National Library of Energy BETA

Sample records for mineral gadolinite ce

  1. CE Geothermal | Open Energy Information

    Open Energy Info (EERE)

    Geothermal Jump to: navigation, search Name: CE Geothermal Place: California Sector: Geothermal energy Product: CE Geothermal previously owned the assets of Western States...

  2. Clay Minerals

    SciTech Connect (OSTI)

    Mueller, Karl T.; Sanders, Rebecca L.; Washton, Nancy M.

    2014-03-14

    Clay minerals are important components of the environment and are involved or implicated in processes such as the uptake of pollutants and the release of nutrients and as potential platforms for a number of chemical reactions. Owing to their small particle sizes (typically, on the order of microns or smaller) and mixing with a variety of other minerals and soil components, advanced characterization methods are needed to study their structures, dynamics, and reactivities. In this article, we describe the use of solid-state NMR methods to characterize the structures and chemistries of clay minerals. Early one-pulse magic-angle spinning (MAS) NMR studies of 27Al and 29Si have now been enhanced and extended with new studies utilizing advanced methodologies (such as Multiple Quantum MAS) as well as studies of less-sensitive nuclei. In additional work, the issue of reactivity of clay minerals has been addressed, including studies of reactive surface area in the environment. Utilizations of NMR-sensitive nuclides within the clay minerals themselves, and in molecules that react with speci?c sites on the clay mineral surfaces, have aided in understanding the reactivity of these complex aluminosilicate systems.

  3. International Refrigeration: Order (2012-CE-1510) | Department...

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    International Refrigeration: Order (2012-CE-1510) International Refrigeration: Order (2012-CE-1510) July 20, 2012 DOE ordered International Refrigeration Products to pay an 8,000 ...

  4. CE Solar | Open Energy Information

    Open Energy Info (EERE)

    Czech Republic Zip: 686 01 Product: Czech PV system integrator primarily building plants for Energy 21 in the Czech Republic. References: CE Solar1 This article is a stub....

  5. CRAD, NNSA - Conduct of Engineering (CE) | Department of Energy

    Office of Environmental Management (EM)

    Conduct of Engineering (CE) CRAD, NNSA - Conduct of Engineering (CE) CRAD for Conduct of Engineering (CE). Criteria Review and Approach Documents (CRADs) that can be used to...

  6. CE: Proposed Penalty (2013-SE-1429)

    Office of Energy Efficiency and Renewable Energy (EERE)

    DOE alleged in a Notice of Proposed Civil Penalty that CE North America, LLC, privately labeled and distributed noncompliant freezers in the U.S.

  7. CE: Compromise Agreement (2013-SE-1429)

    Broader source: Energy.gov [DOE]

    DOE and CE North America entered into a Compromise Agreement to resolve a case involving the distribution in commerce of noncompliant freezers.

  8. Legacy: Order (2015-CE-14025) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Legacy: Order (2015-CE-14025) Legacy: Order (2015-CE-14025) February 11, 2015 DOE ordered The Legacy Companies to pay a $8,000 civil penalty after finding Legacy had failed to certify that refrigerator Maxx-Ice brand basic model MCR3U complies with the applicable energy conservation standards. PDF icon Legacy: Order (2015-CE-14025) More Documents & Publications Legacy: Proposed Penalty (2015-CE-14025) Maxlite: Order (2015-CE-27018) Electrolux: Order (2015-CE-14020)

  9. Thermoelectric Couple Demonstration of (In, Ce)-based Skutterudite...

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    of (In, Ce)-based Skutterudite Materials for Automotive Energy Recovery Thermoelectric Couple Demonstration of (In, Ce)-based Skutterudite Materials for Automotive...

  10. California Ethanol Power CE P | Open Energy Information

    Open Energy Info (EERE)

    Power CE P Jump to: navigation, search Name: California Ethanol & Power (CE+P) Place: Florida Product: US ethanol project developer. References: California Ethanol & Power...

  11. Palmetto Clean Energy (PaCE) Program

    Broader source: Energy.gov [DOE]

    PaCE funding comes from the customers of participating utilities who voluntarily choose to support the program through an additional charge on their monthly utility bills. Of the $4, $3.50 goes t...

  12. CeCap LLP | Open Energy Information

    Open Energy Info (EERE)

    Name: CeCap LLP Place: London, United Kingdom Zip: W1S 2LQ Product: London-based investment boutique which provides investment advice to, and invests in, small to mediun size...

  13. Hybridized Nature of Pseudogap in Kondo Insulators CeRhSb and CeRhAs

    SciTech Connect (OSTI)

    Kumigashira, H.; Takahashi, T.; Yoshii, S.; Kasaya, M.

    2001-08-06

    We studied the electronic structure of Kondo insulators CeRhSb and CeRhAs using high-resolution photoemission spectroscopy. We found that the 4f -derived density of states shows a depletion (pseudogap) at E{sub F} in contrast to metallic Kondo materials. It was found that the size of the f pseudogap is smaller than that of conduction electrons (c pseudogap) while both scale well with the Kondo temperature. The present results indicate that the hybridization between 4f and conduction electrons near E{sub F} is essential for the Kondo gap in the Ce-based compounds.

  14. LG: Order (2015-CE-14022) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    LG: Order (2015-CE-14022) LG: Order (2015-CE-14022) February 11, 2015 DOE ordered LG Electronics USA, Inc. to pay a 8,000 civil penalty after finding LG had failed to certify that ...

  15. Spin reorientation and Ce-Mn coupling in antiferromagnetic oxypnictide CeMnAsO

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Zhang, Qiang; Tian, Wei; Peterson, Spencer G.; Dennis, Kevin W.; Vaknin, David

    2015-02-18

    Structure and magnetic properties of high-quality polycrystlline CeMnAsO, a parent compound of the “1111”-type oxypnictides, have been investigated using neutron powder diffraction and magnetization measurements. We find that CeMnAsO undergoes a C-type antiferromagnetic order with Mn2+(S = 5/2) moments pointing along the c axis below a relatively high Néel temperature of TN = 347(1) K. Below TSR = 35 K, two simultaneous transitions occur where the Mn moments reorient from the c axis to the ab plane preserving the C-type magnetic order, and Ce moments undergo long-range AFM ordering with antiparallel moments pointing in the ab plane. Another transition tomore » a noncollinear magnetic structure occurs below 7 K. The ordered moments of Mn and Ce at 2 K are 3.32(4) μB and 0.81(4)μB, respectively. We find that CeMnAsO primarily falls into the category of a local-moment antiferromagnetic insulator in which the nearest-neighbor interaction (J1) is dominant with J2 < J1/2 in the context of J1 – J2 – Jc model. The spin reorientation transition driven by the coupling between Ce and the transition metal seems to be common to Mn, Fe, and Cr ions, but not to Co and Ni ions in the isostructural oxypnictides. As a result, a schematic illustration of magnetic structures in Mn and Ce sublattices in CeMnAsO is presented.« less

  16. Utility: Order (2016-CE-42007) | Department of Energy

    Energy Savers [EERE]

    CE-42007) Utility: Order (2016-CE-42007) January 5, 2016 DOE ordered Utility Refrigerator to pay a $8,000 civil penalty after finding Utility had failed to certify that certain models of commercial refrigerator equipment comply with the applicable energy conservation standards. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and Utility. PDF icon Utility: Order (2016-CE-42007) More Documents & Publications Utility: Proposed Penalty (2016-CE-42007)

  17. Haier: Order (2011-CE-2104) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Haier: Order (2011-CE-2104) Haier: Order (2011-CE-2104) June 12, 2012 DOE ordered Haier to pay an $20,000 civil penalty after finding Haier had failed to certify that Haier residential clothes dryers comply with the applicable energy conservation standard. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and Haier. PDF icon Haier: 2011-CE-2104 More Documents & Publications Haier: Proposed Penalty (2011-CE-2104) Haier: Noncompliance Determination

  18. Almo: Order (2012-CE-1416) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Almo: Order (2012-CE-1416) Almo: Order (2012-CE-1416) July 25, 2012 DOE ordered Almo Corporation to pay a $6,500 civil penalty after finding Almo had failed to certify that certain models of residential refrigerators comply with the applicable energy conservation standards. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and Almo. PDF icon 2012-CE-1416_Almo_Order More Documents & Publications Almo: Proposed Penalty (2012-CE-1416) International

  19. Electrolux: Order (2012-CE-1901) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Electrolux: Order (2012-CE-1901) Electrolux: Order (2012-CE-1901) July 27, 2012 DOE ordered Electrolux North America to pay a $6,500 civil penalty after finding Electrolux had failed to certify that certain dishwashers comply with the applicable energy conservation standard. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and Electrolux. PDF icon Electrolux: Order (2012-CE-1901) More Documents & Publications Electrolux: Proposed Penalty (2012-CE-1901)

  20. Barron: Order (2013-CE-48004) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Order (2013-CE-48004) Barron: Order (2013-CE-48004) July 15, 2015 DOE ordered Barron Lighting Group, Inc. to pay a $8,000 civil penalty after finding Barron had failed to certify that certain models of illuminated exit signs comply with the applicable energy conservation standards. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and Barron. PDF icon Barron: Order (2013-CE-48004) More Documents & Publications Barron: Proposed Penalty (2013-CE-48004)

  1. PQL: Order (2013-CE-27001) | Department of Energy

    Energy Savers [EERE]

    Order (2013-CE-27001) PQL: Order (2013-CE-27001) August 7, 2015 DOE ordered P.Q.L, Inc. to pay a $12,500 civil penalty after finding PQL had failed to certify that certain models of medium base compact fluorescent lamps comply with the applicable energy conservation standards. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and PQL. PDF icon PQL: Order (2013-CE-27001) More Documents & Publications PQL: Proposed Penalty (2013-CE-27001) PQL: Order

  2. RPI: Order (2015-CE-42065) | Department of Energy

    Energy Savers [EERE]

    Order (2015-CE-42065) RPI: Order (2015-CE-42065) November 6, 2015 DOE ordered RPI Industries, Inc. to pay a $8,000 civil penalty after finding RPI had failed to certify that certain models of commercial refrigeration equipment comply with the applicable energy conservation standards. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and RPI. PDF icon RPI: Order (2015-CE-42065) More Documents & Publications RPI: Proposed Penalty (2015-CE-42065) Maxlite:

  3. Eurodib: Order (2014-CE-45001) | Department of Energy

    Office of Environmental Management (EM)

    Order (2014-CE-45001) Eurodib: Order (2014-CE-45001) May 11, 2015 DOE ordered Eurodib Inc. to pay a $8,000 civil penalty after finding Eurodib had failed to certify that certain models of automatic commercial ice makers comply with the applicable energy conservation standards. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and Eurodib. PDF icon Eurodib: Order (2014-CE-45001) More Documents & Publications Eurodib: Proposed Penalty (2014-CE-45001) Fagor

  4. Maxlite: Order (2015-CE-27018) | Department of Energy

    Office of Environmental Management (EM)

    5-CE-27018) Maxlite: Order (2015-CE-27018) May 14, 2015 DOE ordered Maxlite, Inc. to pay a $8,000 civil penalty after finding Maxlite had failed to certify that certain models of general service fluorescent lamps comply with the applicable energy conservation standards. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and Maxlite. PDF icon Maxlite: Order (2015-CE-27018) More Documents & Publications Maxlite: Proposed Penalty (2015-CE-27018) Maxlite:

  5. Minerals Technologies | Open Energy Information

    Open Energy Info (EERE)

    Technologies Jump to: navigation, search Name: Minerals Technologies Place: Bethlehem, PA Website: www.mineralstechnologies.com References: Minerals Technologies1 Information...

  6. High thermal stability of La2O3 and CeO2-stabilized tetragonal ZrO2

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Wang, Shichao; Xie, Hong; Lin, Yuyuan; Poeppelmeier, Kenneth R.; Li, Tao; Winans, Randall E.; Cui, Yanran; Ribeiro, Fabio H.; Canlas, Christian P.; Elam, Jeffrey W.; et al

    2016-02-15

    Catalyst support materials of tetragonal ZrO2, stabilized by either La2O3 (La2O3-ZrO2) or CeO2 (CeO2-ZrO2), were synthesized under hydrothermal conditions at 200 °C with NH4OH or tetramethylammonium hydroxide as the mineralizer. From In Situ synchrotron powder X-ray diffraction and small-angle X-ray scattering measurements, the calcined La2O3-ZrO2 and CeO2-ZrO2 supports were nonporous nanocrystallites that exhibited rectangular shapes with thermal stability up to 1000 °C in air. These supports had an average size of ~10 nm and a surface area of 59-97 m2/g. The catalysts Pt/La2O3-ZrO2 and Pt/CeO2-ZrO2 were prepared by using atomic layer deposition with varying Pt loadings from 6.3-12.4 wt %.more » Mono-dispersed Pt nanoparticles of ~3 nm were obtained for these catalysts. As a result, the incorporation of La2O3 and CeO2 into the t-ZrO2 structure did not affect the nature of the active sites for the Pt/ZrO2 catalysts for the water-gas-shift (WGS) reaction.« less

  7. Linac Coherent Light SourCe

    Energy Savers [EERE]

    Linac Coherent Light SourCe after the Stanford Linear Accelerator Center (now the SLAC National Accelerator Laboratory) developed its two- mile-long linear accelerator (linac), it received approval from the Department of Energy to construct the Linac Coherent Light Source (LCLS), the first free electron laser (FEL) facility that would be able to produce x-rays short and bright enough that individual molecules could be imaged in their natural states. 40 years Genesis of the idea In 1992, Dr.

  8. Role of Ce4+ in the scintillation mechanism of codoped Gd3Ga3Al2O12:Ce

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Wu, Yuntao; Meng, Fang; Li, Qi; Koschan, Merry; Melcher, Charles L.

    2014-10-17

    To control the time-response performance of widely used cerium-activated scintillators in cutting-edge medical-imaging devices, such as time-of-flight positron-emission tomography, a comprehensive understanding of the role of Ce valence states, especially stable Ce4+, in the scintillation mechanism is essential. However, despite some progress made recently, an understanding of the physical processes involving Ce4+ is still lacking. The aim of this work is to clarify the role of Ce4+ in scintillators by studying Ca2+ codoped Gd3Ga3Al2O12∶Ce (GGAG∶Ce). By using a combination of optical absorption spectra and x-ray absorption near-edge spectroscopies, the correlation between Ca2+codoping content and the Ce4+ fraction is seen. The energy-levelmore » diagrams of Ce3+ and Ce4+ in the Gd3Ga3Al2O12 host are established by using theoretical and experimental methods, which indicate a higher position of the 5d1 state of Ce4+ in the forbidden gap in comparison to that of Ce3+. Underlying reasons for the decay-time acceleration resulting from Ca2+ codoping are revealed, and the physical processes of the Ce4+-emission model are proposed and further demonstrated by temperature-dependent radioluminescence spectra under x-ray excitation.« less

  9. Role of Ce4+ in the scintillation mechanism of codoped Gd3Ga3Al2O12:Ce

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Wu, Yuntao; Meng, Fang; Li, Qi; Koschan, Merry; Melcher, Charles L.

    2014-10-17

    To control the time-response performance of widely used cerium-activated scintillators in cutting-edge medical-imaging devices, such as time-of-flight positron-emission tomography, a comprehensive understanding of the role of Ce valence states, especially stable Ce4+, in the scintillation mechanism is essential. However, despite some progress made recently, an understanding of the physical processes involving Ce4+ is still lacking. The aim of this work is to clarify the role of Ce4+ in scintillators by studying Ca2+ codoped Gd3Ga3Al2O12∶Ce (GGAG∶Ce). By using a combination of optical absorption spectra and x-ray absorption near-edge spectroscopies, the correlation between Ca2+codoping content and the Ce4+ fraction is seen. The energy-levelmore »diagrams of Ce3+ and Ce4+ in the Gd3Ga3Al2O12 host are established by using theoretical and experimental methods, which indicate a higher position of the 5d1 state of Ce4+ in the forbidden gap in comparison to that of Ce3+. Underlying reasons for the decay-time acceleration resulting from Ca2+ codoping are revealed, and the physical processes of the Ce4+-emission model are proposed and further demonstrated by temperature-dependent radioluminescence spectra under x-ray excitation.« less

  10. Oak Ridge Field O%ce

    Office of Legacy Management (LM)

    DOC F ' ;fz; , NiJlo-2- - ' U ' ted St tes Go e e t kh&~~durn Der>artment of Energy rm jl# Oak Ridge Field O%ce DATE: June 21, 1993 REPLY TO ATTW Of: EW-93:Hartman SUBJECT: WAYNE INTERIM STORAGE SITE - TERMINATION OF SITE ENVIRONMENTAL REPORT TO: Peter 3. Gross, Director, Environmental Protection Division, SE-31 The Wayne Interim Storage Site (WISS) is part of the Formerly Utilized Sites Remedial Action Program. Based upon our surveillance efforts at WISS since 1984, the data for all

  11. Atlas Lighting: Order (2015-CE-48001) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Order (2015-CE-48001) Atlas Lighting: Order (2015-CE-48001) July 7, 2015 DOE ordered Atlas Lighting Products to pay a $6,000 civil penalty after finding Atlas Lighting had failed to certify that certain models of illuminated exit signs comply with the applicable energy conservation standards. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and Atlas Lighting. PDF icon Atlas Lighting: Order (2015-CE-48001) More Documents & Publications Atlas Lighting:

  12. Atosa: Order (2015-CE-42037) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Order (2015-CE-42037) Atosa: Order (2015-CE-42037) August 31, 2015 DOE ordered Atosa Catering Equipment, Inc. to pay a $8,000 civil penalty after finding Atosa had failed to certify that certain models of self-contained commercial refrigeration equipment with doors comply with the applicable energy conservation standards. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and Atosa. PDF icon Atosa: Order (2015-CE-42037) More Documents & Publications Atosa:

  13. Goodman Manufacturing: Order (2012-CE-1509) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    2-CE-1509) Goodman Manufacturing: Order (2012-CE-1509) August 7, 2012 DOE ordered Goodman Manufacturing Company L.P. to pay an $8,000 civil penalty after finding Goodman Manufacturing had failed to certify that certain room air conditioners comply with the applicable energy conservation standard. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and Goodman Manufacturing. PDF icon Goodman Manufacturing: Order (2012-CE-1509) More Documents & Publications

  14. Danby Products: Order (2012-CE-1415) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Danby Products: Order (2012-CE-1415) Danby Products: Order (2012-CE-1415) August 9, 2012 DOE ordered Danby Products to pay a $9,900 civil penalty after finding Danby had failed to certify that certain models of refrigerators and freezers comply with the applicable energy conservation standard. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and Danby. PDF icon Danby Products: Order (2012-CE-1415) More Documents & Publications Danby Products: Proposed

  15. Thermoelectric Couple Demonstration of (In, Ce)-based Skutterudite

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Materials for Automotive Energy Recovery | Department of Energy Couple Demonstration of (In, Ce)-based Skutterudite Materials for Automotive Energy Recovery Thermoelectric Couple Demonstration of (In, Ce)-based Skutterudite Materials for Automotive Energy Recovery Presents recent accomplishments and couple test results with these (In, Ce)-based skutterudite TE materials and potential impacts TE power system performance in military and commercial applications PDF icon hendricks_pm.pdf More

  16. Sunpentown: Order (2012-CE-1505) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Order (2012-CE-1505) Sunpentown: Order (2012-CE-1505) August 2, 2012 DOE ordered Sunpentown International Inc. to pay a $12,160 civil penalty after finding Sunpentown had failed to certify that certain models of room air conditioners comply with the applicable energy conservation standards. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and Sunpentown. PDF icon Sunpentown: Order (2012-CE-1505) More Documents & Publications Sunpentown: Proposed Penalty

  17. Eaton Cooper: Order (2015-CE-48003) | Department of Energy

    Office of Environmental Management (EM)

    Order (2015-CE-48003) Eaton Cooper: Order (2015-CE-48003) August 5, 2015 DOE ordered Eaton Cooper Lighting to pay a $8,000 civil penalty after finding Eaton Cooper had failed to certify that certain models of illuminated exit signs comply with the applicable energy conservation standards. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and Eaton Cooper. PDF icon Eaton Cooper: Order (2015-CE-48003) More Documents & Publications Eaton Cooper: Proposed

  18. CE2 Capital Partners LLC | Open Energy Information

    Open Energy Info (EERE)

    Capital Partners LLC Jump to: navigation, search Name: CE2 Capital Partners LLC Place: Solana Beach, California Zip: 92075 Sector: Carbon, Renewable Energy Product:...

  19. Lattice Disorder And Size-Induced Kondo Behavior in CeAl(2) And CePt(2+X)

    SciTech Connect (OSTI)

    Han, S.-W.; Booth, C.H.; Bauer, E.D.; Huang, P.H.; Chen, Y.Y.; Lawrence, J.M.; /LBL, Berkeley /Chonbuk Natl. U. /Los Alamos /Taiwan, Inst. Phys. /UC, Irvine

    2007-07-19

    When the particle size of CeAl{sub 2} and CePt{sub 2+x} samples is reduced to the nanometer scale, antiferromagnetism is suppressed and Kondo behavior dominates. We find that the Kondo temperature T{sub K} can either decrease (CeAl{sub 2}) or increase (CePt{sub 2+x}) in the nanoparticles relative to the bulk. Extended x-ray absorption fine-structure data show that the Ce-Al and Ce-Pt environments are significantly distorted in the nanoparticles. While such distortions should strongly affect magnetic and electronic properties, we find they cannot explain the observed changes in T{sub K}. Changes in the conduction density of states or other parameters must, therefore, play a significant role.

  20. Lattice disorder and size-induced Kondo behavior in CeAl2 andCePt2+x

    SciTech Connect (OSTI)

    Han, S.-W.; Booth, C.H.; Bauer, E.D.; Huang P.H.; Chen, Y.Y.; Lawrence, J.M.

    2006-03-14

    When the particle size of CeAl{sub 2} and CePt{sub 2+x} samples is reduced to the nanometer scale, antiferromagnetism is suppressed and Kondo behavior dominates. We find that the Kondo temperature T{sub K} can either decrease (CeAl{sub 2}) or increase (CePt{sub 2+x}) in the nanoparticles relative to the bulk. Extended x-ray absorption fine-structure data show that the Ce-Al and Ce-Pt environments are significantly distorted in the nanoparticles. While such distortions should strongly affect magnetic and electronic properties, we find they cannot explain the observed changes in T{sub K}. Changes in the conduction density of states or other parameters must, therefore, play a significant role.

  1. Nevada Division of Minerals | Open Energy Information

    Open Energy Info (EERE)

    Logo: Nevada Division of Minerals Name: Nevada Division of Minerals Address: 400 W. King St. 106 Place: Carson City, Nevada Zip: 89703 Website: minerals.state.nv.us...

  2. Hearing protection for miners

    SciTech Connect (OSTI)

    Schulz, T.

    2008-10-15

    A NIOSH analysis showed that at age 50 approximately 90% of coal miners have a hearing impairment, yet noise included hearing loss is 100% preventable. The article discusses requirements of the MSHA regulations, 30 CFR Part 62 - occupational noise exposure (2000) and a 2008-MSHA document describing technologically achievable and promising controls for several types of mining machinery. Hearing protection is still required for exposure to greater than 90 dBA. These are now commercially available ways to determine how much attenuation an individual gets from a given hearing protector, known as 'fit testing'. 3 refs., 1 fig., 1 tab., 1 photo.

  3. Mineral industries of Australia, Canada, and Oceania (including a discussion of Antarctica's mineral resources). Mineral perspective

    SciTech Connect (OSTI)

    Kimbell, C.L.; Lyday, T.Q.; Newman, H.H.

    1985-12-01

    The Bureau of Mines report gives the mineral industry highlights of two of the world's major mineral producing countries, Australia and Canada, and seven Pacific island nations or territories--Fiji, New Caledonia, New Zealand, Papua New Guinea, Republic of Nauru, Solomon Islands, and Vanuatu. The mineral resources of Antarctica are also discussed. Because of the size of the Australian and Canadian mineral industries, summary reviews are presented for each of the States, Provinces, or Territories. The most current information available from all nations is given on major minerals or mineral-commodity production, share of world production, and reserves. Reported also are significant mining companies, locations and capacities of their main facilities, and their share of domestic production. Other information is provided on mineral-related trade with the United States, government mineral policy, energy production-consumption and trade, the mining industry labor force, and prospects for the mineral industry. Maps show the locations of selected mineral deposits, oilfields and gasfields, mines, and processing facilities including iron and steel plants, nonferrous smelters and refineries, and cement plants, as well as infrastructure pertinent to the mineral industry.

  4. Minerals Yearbook: Minerals in the world economy. 1988 International review

    SciTech Connect (OSTI)

    Kimbell, C.L.; Zajac, W.L.

    1988-01-01

    In overview, 1988 appeared to be the best year for the world's mineral industry since 1980, although the all-important petroleum component suffered severely from low prices. With this notable exception, the traditional statistical measures of mineral industry performance, namely production, trade, and consumption, reflected growth in most elements of the world mineral industry from crude material extraction through the gamut of downstream processing. Moreover, the growth was reasonably well distributed geographically, with many countries sharing in the substantial upturn in activity. The report discusses production, trade, consumption, investment, transportation, prices, and statistical summary of world production and trade of major mineral commodities.

  5. Maxlite: Order (2010-CE-2701) | Department of Energy

    Office of Environmental Management (EM)

    0-CE-2701) Maxlite: Order (2010-CE-2701) In the Matter of Maxlite, SK America, Inc. (general service flourescent lamps), DOE Case Number 2010-CE-2701, Adopting Order and Compromise Agreement. Order adopting accompanying Compromise Agreement. DOE found that Maxlite failed to submit compliance certifications for its products under 10 C.F.R. Section 430.62, and here assesses a civil penalty of $5,000 (if paid within 30 days) or of $10,000 (if paid between 31-60 days). Maxlite promises to certify

  6. CE2 Carbon Capital LLC | Open Energy Information

    Open Energy Info (EERE)

    Carbon Capital LLC Jump to: navigation, search Name: CE2 Carbon Capital LLC Place: California Sector: Carbon, Renewable Energy Product: US-based carbon trader that looks to take...

  7. Paragon Sales: Order (2012-CE-1417) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Order (2012-CE-1417) July 30, 2012 DOE ordered Paragon Sales Co., Inc., to pay a 6,000 civil penalty after finding Paragon Sales had failed to certify that certain models of...

  8. Manitowoc Foodservice: Order (2012-CE-5309) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Order (2012-CE-5309) July 20, 2012 DOE ordered Manitowoc Foodservice to pay an 6,000 civil penalty after finding Manitowoc Foodservice had failed to certify that Manitowoc...

  9. Electrolux: Order (2012-CE-1901) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Order (2012-CE-1901) July 27, 2012 DOE ordered Electrolux North America to pay a 6,500 civil penalty after finding Electrolux had failed to certify that certain dishwashers comply...

  10. Haier: Order (2011-CE-2104) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Haier: Order (2011-CE-2104) June 12, 2012 DOE ordered Haier to pay an 20,000 civil penalty after finding Haier had failed to certify that Haier residential clothes...

  11. Danby Products: Order (2012-CE-1415) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Order (2012-CE-1415) August 9, 2012 DOE ordered Danby Products to pay a 9,900 civil penalty after finding Danby had failed to certify that certain models of refrigerators...

  12. Utility: Proposed Penalty (2016-CE-42007) | Department of Energy

    Energy Savers [EERE]

    Proposed Penalty (2016-CE-42007) Utility: Proposed Penalty (2016-CE-42007) November 30, 2015 DOE alleged in a Notice of Proposed Civil Penalty that Utility Refrigerator failed to certify certain commercial refrigerator equipment as compliant with the applicable energy conservation standards. DOE regulations require a manufacturer (which includes importers) to submit reports certifying that its products have been tested and meet the applicable energy conservation standards. This civil penalty

  13. International Refrigeration: Order (2012-CE-1510) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    International Refrigeration: Order (2012-CE-1510) International Refrigeration: Order (2012-CE-1510) July 20, 2012 DOE ordered International Refrigeration Products to pay an $8,000 civil penalty after finding International Refrigeration had failed to certify that certain room air conditioners comply with the applicable energy conservation standard. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and International Refrigeration. PDF icon International

  14. Atlas Lighting: Proposed Penalty (2015-CE-48001) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Proposed Penalty (2015-CE-48001) Atlas Lighting: Proposed Penalty (2015-CE-48001) June 2, 2015 DOE alleged in a Notice of Proposed Civil Penalty that Atlas Lighting Products failed to certify a variety of illuminated exit sign basic models as compliant with the applicable energy conservation standards. DOE regulations require a manufacturer (which includes importers) to submit reports certifying that its products have been tested and meet the applicable energy conservation standards. This civil

  15. Atosa: Proposed Penalty (2015-CE-42037) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Proposed Penalty (2015-CE-42037) Atosa: Proposed Penalty (2015-CE-42037) August 10, 2015 DOE alleged in a Notice of Proposed Civil Penalty that Atosa Catering Equipment, Inc. failed to certify various models of self-contained commercial refrigeration equipment with doors as compliant with the applicable energy conservation standards. DOE regulations require a manufacturer (which includes importers) to submit reports certifying that its products have been tested and meet the applicable energy

  16. Distinctive Appliances: Order (2015-CE-14019) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Distinctive Appliances: Order (2015-CE-14019) Distinctive Appliances: Order (2015-CE-14019) February 19, 2015 DOE ordered Distinctive Appliances Distributing, Inc. to pay a $16,000 civil penalty after finding Distinctive Appliances had failed to certify that certain models of Fhiaba-brand refrigerator-freezers comply with the applicable energy conservation standards. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and Distinctive Appliances. PDF icon

  17. Barron: Proposed Penalty (2013-CE-48004) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Proposed Penalty (2013-CE-48004) Barron: Proposed Penalty (2013-CE-48004) June 12, 2015 DOE alleged in a Notice of Proposed Civil Penalty that Barron Lighting Group, Inc. failed to certify a variety of illuminated exit sign models as compliant with the applicable energy conservation standards. DOE regulations require a manufacturer (which includes importers) to submit reports certifying that its products have been tested and meet the applicable energy conservation standards. This civil penalty

  18. Systemair: Order (2016-CE-43003) | Department of Energy

    Energy Savers [EERE]

    Systemair: Order (2016-CE-43003) Systemair: Order (2016-CE-43003) February 23, 2016 DOE ordered Systemair, Inc., to pay a $8,000 civil penalty after finding Systemair had failed to certify that its single package vertical air conditioning and heating equipment comply with the applicable energy conservation standards. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and Systemair. DOE regulations require a manufacturer (which includes importers) to submit

  19. True: Order (2015-CE-42049) | Department of Energy

    Energy Savers [EERE]

    True: Order (2015-CE-42049) True: Order (2015-CE-42049) February 4, 2016 DOE ordered True Manufacturing Co., Inc., to pay a $36,400 civil penalty after finding True had manufactured and distributed in commerce in the U.S. 182 units of True commercial refrigerator basic models TCGG-72 and GCGG-72-S, which did not meet the application energy conservation standard. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and True. Federal law subjects manufacturers and

  20. Sanyo Electric: Order (2010-CE-1210) | Department of Energy

    Energy Savers [EERE]

    Sanyo Electric: Order (2010-CE-1210) Sanyo Electric: Order (2010-CE-1210) October 13, 2010 DOE issued an Order and entered into a Compromise Agreement with Sanyo E&E Corp. after finding Sanyo had used an improper method to submit its certification that certain models of residential refrigerators, refrigerator-freezers, and freezers comply with the applicable energy conservation standards. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and Sanyo. PDF

  1. PQL: Proposed Penalty (2013-CE-27001) | Department of Energy

    Energy Savers [EERE]

    Proposed Penalty (2013-CE-27001) PQL: Proposed Penalty (2013-CE-27001) July 10, 2015 DOE alleged in a Notice of Proposed Civil Penalty that P.Q.L., Inc. failed to certify various basic models of medium base compact fluorescent lamps as compliant with the applicable energy conservation standards. DOE regulations require a manufacturer (which includes importers) to submit reports certifying that its products have been tested and meet the applicable energy conservation standards. This civil penalty

  2. RPI: Proposed Penalty (2015-CE-42065) | Department of Energy

    Energy Savers [EERE]

    Proposed Penalty (2015-CE-42065) RPI: Proposed Penalty (2015-CE-42065) September 25, 2015 DOE alleged in a Notice of Proposed Civil Penalty that RPI Industries, Inc. failed to certify various basic models of self-contained refrigeration equipment with doors as compliant with the applicable energy conservation standards. DOE regulations require a manufacturer (which includes importers) to submit reports certifying that its products have been tested and meet the applicable energy conservation

  3. Eurodib: Proposed Penalty (2014-CE-45001) | Department of Energy

    Office of Environmental Management (EM)

    Proposed Penalty (2014-CE-45001) Eurodib: Proposed Penalty (2014-CE-45001) March 4, 2015 DOE alleged in a Notice of Proposed Civil Penalty that Eurodib Inc. failed to certify automatic commercial ice makers as compliant with the applicable energy conservation standards. DOE regulations require a manufacturer (which includes importers) to submit reports certifying that its products have been tested and meet the applicable energy conservation standards. This civil penalty notice advises the

  4. Fujitsu: Order (2015-CE-16014) | Department of Energy

    Office of Environmental Management (EM)

    Fujitsu: Order (2015-CE-16014) Fujitsu: Order (2015-CE-16014) October 27, 2015 DOE ordered Fujitsu General America, Inc. to pay a $8,000 civil penalty after finding Fujitsu had failed to certify that certain models of central air conditioners and heat pumps comply with the applicable energy conservation standards prior to distributing them in commerce. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and Fujitsu. DOE regulations require a manufacturer (which

  5. Lochinvar: Order (2016-CE-24001) | Department of Energy

    Office of Environmental Management (EM)

    Lochinvar: Order (2016-CE-24001) Lochinvar: Order (2016-CE-24001) November 2, 2015 DOE ordered Lochinvar, LLC, to pay a $8,000 civil penalty after finding Lochinvar had failed to certify that certain models of pool heaters comply with the applicable energy conservation standard. The Order adopted a Compromise Agreement, which reflected settlement terms between DOE and Lochinvar. DOE regulations require a manufacturer (which includes importers) to submit reports certifying that its products have

  6. Maxlite: Proposed Penalty (2015-CE-27018) | Department of Energy

    Office of Environmental Management (EM)

    Proposed Penalty (2015-CE-27018) Maxlite: Proposed Penalty (2015-CE-27018) May 6, 2015 DOE alleged in a Notice of Proposed Civil Penalty that Maxlite, Inc. failed to certify general service fluorescent lamps as compliant with the applicable energy conservation standards. DOE regulations require a manufacturer (which includes importers) to submit reports certifying that its products have been tested and meet the applicable energy conservation standards. This civil penalty notice advises the

  7. EIS-0497: CE FLNG Project, Plaquemines Parish, Louisiana | Department of

    Office of Environmental Management (EM)

    Energy 7: CE FLNG Project, Plaquemines Parish, Louisiana EIS-0497: CE FLNG Project, Plaquemines Parish, Louisiana Summary The Federal Energy Regulatory Commission (FERC) is preparing, with DOE as a cooperating agency, an EIS to analyze the potential environmental impacts of a proposal to construct and operate a liquefied natural gas terminal in Plaquemines Parish, Louisiana, and approximately 37 miles of 42-inch diameter natural gas transmission pipeline to connect the terminal to natural

  8. Eaton Cooper: Proposed Penalty (2015-CE-48003) | Department of Energy

    Office of Environmental Management (EM)

    Proposed Penalty (2015-CE-48003) Eaton Cooper: Proposed Penalty (2015-CE-48003) June 16, 2015 DOE alleged in a Notice of Proposed Civil Penalty that Eaton Cooper Lighting failed to certify a variety of illuminated exit sign models as compliant with the applicable energy conservation standards. DOE regulations require a manufacturer (which includes importers) to submit reports certifying that its products have been tested and meet the applicable energy conservation standards. This civil penalty

  9. Ca2+-Doped CeBr3 Scintillating Materials

    SciTech Connect (OSTI)

    Guss, Paul; Foster, Michael E.; Wong, Bryan M.; Doty, F. Patrick; Shah, Kanai; Squillante, Michael R.; Shirwadkar, Urmila; Hawrami, Rastgo; Tower, Josh; Yuan, Ding

    2014-01-21

    Despite the outstanding scintillation performance characteristics of cerium tribromide (CeBr3) and cerium-activated lanthanum tribromide, their commercial availability and application are limited due to the difficulties of growing large, crack-free single crystals from these fragile materials. This investigation employed aliovalent doping to increase crystal strength while maintaining the optical properties of the crystal. One divalent dopant (Ca2+) was used as a dopant to strengthen CeBr3 without negatively impacting scintillation performance. Ingots containing nominal concentrations of 1.9% of the Ca2+ dopant were grown. Preliminary scintillation measurements are presented for this aliovalently doped scintillator. Ca2+-doped CeBr3 exhibited little or no change in the peak fluorescence emission for 371 nm optical excitation for CeBr3. The structural, electronic, and optical properties of CeBr3 crystals were studied using the density functional theory within the generalized gradient approximation. The calculated lattice parameters are in good agreement with the experimental data. The energy band structures and density of states were obtained. The optical properties of CeBr3, including the dielectric function, were calculated.

  10. Universal ripper miner

    DOE Patents [OSTI]

    Morrell, Roger J. (Bloomington, MN); Larson, David A. (Minneapolis, MN)

    1991-01-01

    A universal ripper miner used to cut, collect and transfer material from an underground mine working face includes a cutter head that is vertically movable in an arcuate cutting cycle by means of drive members, such as hydraulically actuated pistons. The cutter head may support a circular cutter bit having a circular cutting edge that may be indexed to incrementally expose a fresh cutting edge. An automatic indexing system is disclosed wherein indexing occurs by means of a worm gear and indexing lever mechanism. The invention also contemplates a bi-directional bit holder enabling cutting to occur in both the upstroke and the downstroke cutting cycle. Another feature of the invention discloses multiple bits arranged in an in-line, radially staggered pattern, or a side-by-side pattern to increase the mining capacity in each cutting cycle. An on-board resharpening system is also disclosed for resharpening the cutting edge at the end of cutting stroke position. The aforementioned improvement features may be used either singly, or in any proposed combination with each other.

  11. Comparison of the high-pressure behavior of the cerium oxides Ce2O3 and CeO2

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Lipp, M. J.; Jeffries, J. R.; Cynn, H.; Park Klepeis, J. -H.; Evans, W. J.; Mortensen, D. R.; Seidler, G. T.; Xiao, Y.; Chow, P.

    2016-02-09

    We studied the high-pressure behavior of Ce2O3 using angle-dispersive x-ray diffraction to 70 GPa and compared with that of CeO2. Up to the highest pressure Ce2O3 remains in the hexagonal phase (space group 164, P ¯32/m1) typical for the lanthanide sesquioxides. We did not observe a theoretically predicted phase instability for 30 GPa. The isothermal bulk modulus and its pressure derivative for the quasihydrostatic case are B0 = 111 ± 2 GPa, B'0 = 4.7 ± 0.3, and for the case without pressure-transmitting medium B0 = 104 ±4 GPa, B'0 = 6.5 ± 0.4. Starting from ambient-pressure magnetic susceptibility measurementsmore » for both oxides in highly purified form,we find that the Ce atom in Ce2O3 behaves like a trivalent Ce3+ ion (2.57μB per Ce atom) in contrast to previously published data. Since x-ray emission spectroscopy of the Lγ (4d3/2 → 2p1/2) transition is sensitive to the 4f -electron occupancy, we also followed the high-pressure dependence of this line for both oxides up to 50 GPa. We observed no change of the respective line shape, indicating that the 4f -electron configuration is stable for both materials. We posit from this data that the 4f electrons do not drive the volume collapse of CeO2 from the high-symmetry, low-pressure fluorite structure to the lower-symmetry orthorhombic phase.« less

  12. Effects of CeO2 Support Facets on VOx/CeO2 Catalysts in Oxidative Dehydrogenation of Methanol

    SciTech Connect (OSTI)

    Li, Yan; Wei, Zhehao; Gao, Feng; Kovarik, Libor; Peden, Charles HF; Wang, Yong

    2014-05-13

    CeO2 supports with dominating facets, i.e., low index (100), (110) and (111) facets, are prepared. The facet effects on the structure and catalytic performance of supported vanadium oxide catalysts are investigated using oxidative dehydrogenation of methanol as a model reaction. In the presence of mixed facets, Infrared and Raman characterizations demonstrate that surface vanadia species preferentially deposit on CeO2 (100) facets, presumably because of its higher surface energy. At the same surface vanadium densities, VOx species on (100) facets show better dispersion, followed by (110) and (111) facets. The VOx species on CeO2 nanorods with (110) and (100) facets display higher activity and lower apparent activation energies compared to that on CeO2 nanopolyhedras with dominating (111) facets and CeO2 nanocubes with dominating (100) facets. The higher activity for VOx/CeO2(110) might be related to the more abundant oxygen vacancies present on the (110) facets, evidenced from Raman spectroscopic measurements.

  13. Property:MineralManager | Open Energy Information

    Open Energy Info (EERE)

    MineralManager Jump to: navigation, search Property Name MineralManager Property Type Page Pages using the property "MineralManager" Showing 25 pages using this property. (previous...

  14. China Gengsheng Minerals Inc | Open Energy Information

    Open Energy Info (EERE)

    Gengsheng Minerals Inc Jump to: navigation, search Name: China Gengsheng Minerals Inc Place: Henan Province, China Product: China-based material technology company. References:...

  15. Energy and Mineral Development Program

    Office of Environmental Management (EM)

    - Federal Register Solicitation ◦ FY 2012 very soon ◦ Average 60-90+ days response from tribes Annual Funding Program - Energy and Mineral Development Projects ◦ Renewable: Biomass (Woody, Waste-to-Energy), Wind, Hydroelectric, Geothermal, and Solar ◦ Oil, Gas, and Coal ◦ Mineral - Pre-Development work: ◦ Resource Assessment/Exploration studies ◦ Feasibility studies ◦ Market studies In previous years a por tion of the program has been earmarked for renewable energy projects and

  16. An Update on NiCE Support for BISON

    SciTech Connect (OSTI)

    McCaskey, Alex; Billings, Jay Jay; Deyton, Jordan H.; Wojtowicz, Anna

    2015-09-01

    The Nuclear Energy Advanced Modeling and Simulation program (NEAMS) from the Department of Energy s Office of Nuclear Energy has funded the development of a modeling and simulation workflow environment to support the various codes in its nuclear energy scientific computing toolkit. This NEAMS Integrated Computational Environment (NiCE) provides extensible tools and services that enable efficient code execution, input generation, pre-processing visualizations, and post-simulation data analysis and visualization for a large portion of the NEAMS Toolkit. A strong focus for the NiCE development team throughout FY 2015 has been support for the Multiphysics Object Oriented Simulation Environment (MOOSE) and the NEAMS nuclear fuel performance modeling application built on that environment, BISON. There is a strong desire in the program to enable and facilitate the use of BISON throughout nuclear energy research and industry. A primary result of this desire is the need for strong support for BISON in NiCE. This report will detail improvements to NiCE support for BISON. We will present a new and improved interface for interacting with BISON simulations in a variety of ways: (1) improved input model generation, (2) embedded mesh and solution data visualizations, and (3) local and remote BISON simulation launch. We will also show how NiCE has been extended to provide support for BISON code development.

  17. Minerals in the world economy. Minerals yearbook Volume 3. 1991 international review

    SciTech Connect (OSTI)

    Kimbell, C.L.

    1991-12-31

    This edition of the Minerals Yearbook - International Review records the performance of the worldwide minerals industry during 1991 and provides background information to assist in interpreting that performance. Volume III, International Review, contains the latest available mineral data on more than 150 foreign countries and discusses the importance of minerals to the economies of these nations. The 1991 review is presented as five area reports and one world overview: Mineral Industries of Africa, Mineral Industries of Asia and the Pacific, Mineral Industries of Latin America and Canada, Mineral Industries of Europe and the U.S.S.R., Mineral Industries of the Middle East, and Minerals in the World Economy.

  18. Homoleptic Ce(III) and Ce(IV) Nitroxide Complexes: Significant Stabilization of the 4+ Oxidation State

    SciTech Connect (OSTI)

    Bogart, Justin A.; Lewis, Andrew J.; Medling, Scott A.; Piro, Nicholas A.; Carroll, Patrick J.; Booth, Corwin H.; Schelter, Eric J.

    2014-06-25

    Electrochemical experiments performed on the complex Ce-IV[2-((BuNO)-Bu-t)py](4), where [2-((BuNO)-Bu-t)py](-) = N-tert-butyl-N-2-pyridylnitroxide, indicate a 2.51 V stabilization of the 4+ oxidation state of Ce compared to [(Bu4N)-Bu-n](2)[Ce(NO3)(6)] in acetonitrile and a 2.95 V stabilization compared to the standard potential for the ion under aqueous conditions. Density functional theory calculations suggest that this preference for the higher oxidation state is a result of the tetrakis(nitroxide) ligand framework at the Ce cation, which allows for effective electron donation into, and partial covalent overlap with, vacant 4f orbitals with delta symmetry. The results speak to the behavior of CeO2 and related solid solutions in oxygen uptake and transport applications, in particular an inherent local character of bonding that stabilizes the 4+ oxidation state. The results indicate a cerium(IV) complex that has been stabilized to an unprecedented degree through tuning of its ligand-field environment.

  19. CRYSTAL CHEMISTRY OF HYDROUS MINERALS

    SciTech Connect (OSTI)

    Y. ZHAO; ET AL

    2001-02-01

    Hydrogen has long been appreciated for its role in geological processes of the Earth's crust. However, its role in Earth's deep interior has been neglected in most geophysical thinking. Yet it is now believed that most of our planet's hydrogen may be locked up in high pressure phases of hydrous silicate minerals within the Earth's mantle. This rocky interior (approximately 7/8 of Earth's volume) is conjectured to contain 1-2 orders of magnitude more water than the more obvious oceans (the ''hydrosphere'') and atmosphere. This project is aimed at using the capability of neutron scattering from hydrogen to study the crystal chemistry and stability of hydrogen-bearing minerals at high pressures and temperatures. At the most basic level this is a study of the atomic position and hydrogen bond itself. We have conducted experimental runs on hydrous minerals under high pressure and high temperature conditions. The crystallographic structure of hydrous minerals at extreme conditions and its structural stability, and hydrogen bond at high P-T conditions are the fundamental questions to be addressed. The behavior of the hydrous minerals in the deep interior of the Earth has been discussed.

  20. Proactive Design of n-Type (In, Ce) Filled Skutterudites Enabling...

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Design of n-Type (In, Ce) Filled Skutterudites Enabling High-Temperature Waste Heat Recovery Proactive Design of n-Type (In, Ce) Filled Skutterudites Enabling High-Temperature ...

  1. SEMI-ANNUAL REPORTS FOR CE FLNG, LLC (CAMBRIDGE) - DK. NO. 12...

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    CE FLNG, LLC (CAMBRIDGE) - DK. NO. 12-123-LNG - ORDER 3193 SEMI-ANNUAL REPORTS FOR CE FLNG, LLC (CAMBRIDGE) - DK. NO. 12-123-LNG - ORDER 3193 PDF icon April 2013 PDF icon October...

  2. DOI-BLM-ID-110-2009-3825-CE | Open Energy Information

    Open Energy Info (EERE)

    110-2009-3825-CE Jump to: navigation, search NEPA Document Collection for: DOI-BLM-ID-110-2009-3825-CE CX at Crane Creek Geothermal Area for GeothermalExploration Crane Creek...

  3. CO Oxidation mechanism on CeO2-supported Au nanoclusters

    SciTech Connect (OSTI)

    Kim H. Y.; Henkelman, G.

    2013-09-08

    To reveal the richer chemistry of CO oxidation by CeO2 supported Au Nanoclusters(NCs)/Nanoparticles, we design Au13 and Au12 supported on a flat and a stepped-CeO2 model (Au/CeO2) and study various kinds of CO oxidation mechanisms at the Au-CeO2 interface and the Au NC as well.

  4. Neutron scattering of CeNi at the SNS-ORNL: A preliminary report

    SciTech Connect (OSTI)

    Mirmelstein, A. [Russian Federal Nuclear Center VNIITF, Snezhinsk, Russia; Podlesnyak, Andrey A [ORNL; Kolesnikov, Alexander I [ORNL; Saporov, B. [Oak Ridge National Laboratory (ORNL); Sefat, A.S. [Oak Ridge National Laboratory (ORNL); Tobin, J. G. [Lawrence Livermore National Laboratory (LLNL)

    2014-01-01

    This is a preliminary report of a neutron scattering experiment used to investigate 4f electron behavior in Ce.

  5. Lattice Disorder and Size-Induced Kondo Behavior in CeAl{sub 2} and CePt{sub 2+x}

    SciTech Connect (OSTI)

    Han, S.-W.; Booth, C. H.; Bauer, E. D.; Huang, P. H.; Chen, Y. Y.; Lawrence, J. M.

    2006-09-01

    When the size of CeAl{sub 2} and CePt{sub 2+x} particles is reduced to the nanometer scale, antiferromagnetism is suppressed and Kondo behavior predominates, with the Kondo temperature T{sub K} either decreasing (CeAl{sub 2}) or increasing (CePt{sub 2+x}) relative to the bulk. Local structure measurements show that these nanoparticles are significantly distorted. While such distortions should strongly affect magnetic and electronic properties, we find they cannot explain the observed changes in T{sub K}. Other size-induced changes to the electronic structure must, therefore, play a significant role.

  6. Review of 1989 international mineral industry activities

    SciTech Connect (OSTI)

    Kimbell, C.L. (US Bureau of Mines, Washington, DC (US))

    1990-07-01

    This article reviews global mineral industry activities for 1989. Production of coal, natural gas, and petroleum, as well as non-fuel minerals, is detailed regionally and for individual countries. The problems of changes in technology, economic and political systems are discussed where they have affected mineral production.

  7. LOW TEMPERATURE GEOTHERMAL MINERAL RECOVERY PROGRAM 02/11/2014...

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    LOW TEMPERATURE GEOTHERMAL MINERAL RECOVERY PROGRAM 02112014 LOW TEMPERATURE GEOTHERMAL MINERAL RECOVERY PROGRAM 02112014 PDF icon mineral-webinar.pdf More Documents & ...

  8. New Mexico Energy, Minerals and Natural Resources Department...

    Open Energy Info (EERE)

    Minerals and Natural Resources Department Jump to: navigation, search Logo: New Mexico Energy, Minerals and Natural Resources Department Name: New Mexico Energy, Minerals...

  9. Oregon Department of Geology and Mineral Industries | Open Energy...

    Open Energy Info (EERE)

    Geology and Mineral Industries Jump to: navigation, search Logo: Oregon Department of Geology and Mineral Industries Name: Oregon Department of Geology and Mineral Industries...

  10. Mineralization of Carbon Dioxide: Literature Review

    SciTech Connect (OSTI)

    Romanov, V; Soong, Y; Carney, C; Rush, G; Nielsen, B; O'Connor, W

    2015-01-01

    CCS research has been focused on CO2 storage in geologic formations, with many potential risks. An alternative to conventional geologic storage is carbon mineralization, where CO2 is reacted with metal cations to form carbonate minerals. Mineralization methods can be broadly divided into two categories: in situ and ex situ. In situ mineralization, or mineral trapping, is a component of underground geologic sequestration, in which a portion of the injected CO2 reacts with alkaline rock present in the target formation to form solid carbonate species. In ex situ mineralization, the carbonation reaction occurs above ground, within a separate reactor or industrial process. This literature review is meant to provide an update on the current status of research on CO2 mineralization. 2

  11. Strata control in mineral engineering

    SciTech Connect (OSTI)

    Bieniawski, Z.T.

    1986-01-01

    This book covers the state-of-the-art of strata control practice both in the United States and abroad with respect to strata reinforcement by rock bolting, long wall mining technology and innovations in energy development, such as mining for oil and tunneling for storage of high-level nuclear waste in deep underground repositories. It features coverage of design concepts in rock engineering and rockbolt systems, stability of rock pillars, rockbursts, shaft design and construction and a detailed consideration of mineral and energy needs in the United States.

  12. Mineral Resource Information System for Field Lab in the Osage Mineral Reservation Estate

    SciTech Connect (OSTI)

    Carroll, H.B.; Johnson, William I.

    1999-04-27

    The Osage Mineral Reservation Estate is located in Osage County, Oklahoma. Minerals on the Estate are owned by members of the Osage Tribe who are shareholders in the Estate. The Estate is administered by the Osage Agency, Branch of Minerals, operated by the U.S. Bureau of Indian Affairs (BIA). Oil, natural gas, casinghead gas, and other minerals (sand, gravel, limestone, and dolomite) are exploited by lessors. Operators may obtain from the Branch of Minerals and the Osage Mineral Estate Tribal Council leases to explore and exploit oil, gas, oil and gas, and other minerals on the Estate. Operators pay a royalty on all minerals exploited and sold from the Estate. A mineral Resource Information system was developed for this project to evaluate the remaining hydrocarbon resources located on the Estate. Databases on Microsoft Excel spreadsheets of operators, leases, and production were designed for use in conjunction with an evaluation spreadsheet for estimating the remaining hydrocarbons on the Estate.

  13. On the heat capacity of Ce{sub 3}Al

    SciTech Connect (OSTI)

    Singh, Durgesh Samatham, S. Shanmukharao Venkateshwarlu, D. Gangrade, Mohan Ganesan, V.

    2014-04-24

    Electrical resistivity and heat capacity measurements on Cerium based dense Kondo compound Ce{sub 3}Al have been reported. Clear signatures of first order structural transition at 108K, followed by a Kondo minimum and coherence are clearly seen in resistivity. The structural transition is robust and is not affected by magnetic fields. Heat capacity measurements reveal an anomalous enhancement in the heavy fermion character upon magnetic fields. Vollhardt invariance in specific heat C(T.H) curves have been observed at T=3.7K and at H ? 6T.

  14. The influence of nano-architectured CeOx supports in RhPd/CeO? for the catalytic ethanol steam reforming reaction

    SciTech Connect (OSTI)

    Divins, N. J.; Senanayake, S. D.; Casanovas, A.; Xu, W.; Trovarelli, A.; Llorca, J.

    2015-01-19

    The ethanol steam reforming (ESR) reaction has been tested over RhPd supported on polycrystalline ceria in comparison to structured supports composed of nanoshaped CeO? cubes and CeO? rods tailored towards the production of hydrogen. At 650-700 K the hydrogen yield follows the trend RhPd/CeO?-cubes > RhPd/CeO? -rods > RhPd/CeO?- polycrystalline, whereas at temperatures higher than 800 K the catalytic performance of all samples is similar and close to the thermodynamic equilibrium. The improved performance of RhPd/CeO?-cubes and RhPd/CeO? -rods for ESR at low temperature is mainly ascribed to higher water-gas shift activity and a strong interaction between the bimetallic - oxide support interaction. STEM analysis shows the existence of RhPd alloyed nanoparticles in all samples, with no apparent relationship between ESR performance and RhPd particle size. X-ray diffraction under operating conditions shows metal reorganization on {100} and {110} ceria crystallographic planes during catalyst activation and ESR, but not on {111} ceria crystallographic planes. The RhPd reconstructing and tuned activation over ceria nanocubes and nanorods is considered the main reason for better catalytic activity with respect to conventional catalysts based on polycrystalline ceria

  15. The influence of nano-architectured CeOx supports in RhPd/CeO₂ for the catalytic ethanol steam reforming reaction

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Divins, N. J.; Senanayake, S. D.; Casanovas, A.; Xu, W.; Trovarelli, A.; Llorca, J.

    2015-01-19

    The ethanol steam reforming (ESR) reaction has been tested over RhPd supported on polycrystalline ceria in comparison to structured supports composed of nanoshaped CeO₂ cubes and CeO₂ rods tailored towards the production of hydrogen. At 650-700 K the hydrogen yield follows the trend RhPd/CeO₂-cubes > RhPd/CeO₂ -rods > RhPd/CeO₂- polycrystalline, whereas at temperatures higher than 800 K the catalytic performance of all samples is similar and close to the thermodynamic equilibrium. The improved performance of RhPd/CeO₂-cubes and RhPd/CeO₂ -rods for ESR at low temperature is mainly ascribed to higher water-gas shift activity and a strong interaction between the bimetallic -more » oxide support interaction. STEM analysis shows the existence of RhPd alloyed nanoparticles in all samples, with no apparent relationship between ESR performance and RhPd particle size. X-ray diffraction under operating conditions shows metal reorganization on {100} and {110} ceria crystallographic planes during catalyst activation and ESR, but not on {111} ceria crystallographic planes. The RhPd reconstructing and tuned activation over ceria nanocubes and nanorods is considered the main reason for better catalytic activity with respect to conventional catalysts based on polycrystalline ceria« less

  16. Interface Induced Carbonate Mineralization: A Fundamental Geochemical

    Office of Scientific and Technical Information (OSTI)

    Process Relevant to Carbon Sequestration (Technical Report) | SciTech Connect Interface Induced Carbonate Mineralization: A Fundamental Geochemical Process Relevant to Carbon Sequestration Citation Details In-Document Search Title: Interface Induced Carbonate Mineralization: A Fundamental Geochemical Process Relevant to Carbon Sequestration We have approached the long-standing geochemical question why anhydrous high-Mg carbonate minerals (i.e., magnesite and dolomite) cannot be formed at

  17. Center for Excitonics (CE) | U.S. DOE Office of Science (SC)

    Office of Science (SC) Website

    Center for Excitonics (CE) Energy Frontier Research Centers (EFRCs) EFRCs Home Centers EFRC External Websites Research Science Highlights News & Events Publications History Contact BES Home Centers Center for Excitonics (CE) Print Text Size: A A A FeedbackShare Page CE Header Director Marc Baldo Lead Institution Massachusetts Institute of Technology Year Established 2009 Mission To supersede traditional electronics with devices that use excitonics to mediate the flow of energy. Research

  18. Proactive Design of n-Type (In, Ce) Filled Skutterudites Enabling

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    High-Temperature Waste Heat Recovery | Department of Energy Design of n-Type (In, Ce) Filled Skutterudites Enabling High-Temperature Waste Heat Recovery Proactive Design of n-Type (In, Ce) Filled Skutterudites Enabling High-Temperature Waste Heat Recovery Thermoelectric and structural properties of n-type (In, Ce) filled skutterudites including power factors and ZT as a function of temperature are presented PDF icon subramanian.pdf More Documents & Publications Proactive Design of n-Type

  19. Geology and Minerals | Open Energy Information

    Open Energy Info (EERE)

    Jump to: navigation, search Retrieved from "http:en.openei.orgwindex.php?titleGeologyandMinerals&oldid612244" Feedback Contact needs updating Image needs updating...

  20. Interface Induced Carbonate Mineralization: A Fundamental Geochemical

    Office of Scientific and Technical Information (OSTI)

    Interface Induced Carbonate Mineralization: A Fundamental Geochemical Process Relevant to Carbon Sequestration Teng, H. Henry PI, The George Washington University PI, The George...

  1. Ethanol Steam Reforming on Co/CeO2: The Effect of ZnO Promoter

    SciTech Connect (OSTI)

    Davidson, Stephen; Sun, Junming; Wang, Yong

    2013-12-02

    A series of ZnO promoted Co/CeO2 catalysts were synthesized and characterized using XRD, TEM, H2-TPR, CO chemisorption, O2-TPO, IR-Py, and CO2-TPD. The effects of ZnO on the catalytic performances of Co/CeO2 were studied in ethanol steam reforming. It was found that the addition of ZnO facilitated the oxidation of Co0 via enhanced oxygen mobility of the CeO2 support which decreased the activity of Co/CeO2 in CC bond cleavage of ethanol. 3 wt% ZnO promoted Co/CeO2 exhibited minimum CO and CH4 selectivity and maximum CO2 selectivity. This resulted from the combined effects of the following factors with increasing ZnO loading: (1) enhanced oxygen mobility of CeO2 facilitated the oxidation of CHx and CO to form CO2; (2) increased ZnO coverage on CeO2 surface reduced the interaction between CHx/CO and Co/CeO2; and (3) suppressed CO adsorption on Co0 reduced CO oxidation rate to form CO2. In addition, the addition of ZnO also modified the surface acidity and basicity of CeO2, which consequently affected the C2C4 product distributions.

  2. Capillary electrophoresis-fluorescence line narrowing system (CE-FLNS) for on-line structural characterization

    DOE Patents [OSTI]

    Jankowiak, R.J.; Small, G.J.; Shields, P.A.

    1999-04-27

    Capillary electrophoresis (CE) is interfaced with low temperature fluorescence line-narrowing (FLN) spectroscopy for on-line structural characterization of separated molecular analytes. 21 figs.

  3. Capillary electrophoresis-fluorescence line narrowing system (CE-FLNS) for on-line structural characterization

    DOE Patents [OSTI]

    Jankowiak, Ryszard J. (Ames, IA); Small, Gerald J. (Ames, IA); Shields, Peter A. (Reading, MA)

    1999-04-27

    Capillary electrophoresis (CE) is interfaced with low temperature fluorescence line-narrowing (FLN) spectroscopy for on-line structural characterization of separated molecular analytes.

  4. Luminescence properties of LaF{sub 3}:Ce nanoparticles encapsulated by oleic acid

    SciTech Connect (OSTI)

    Kim, Jaewoo; Lee, Jun-Hyung; An, Hyejin; Lee, Jungkuk; Park, Seong-Hee; Seo, Young-Soo; Miller, William H.

    2014-09-15

    Highlights: In-situ hydrophobization of water dispersible LaF{sub 3}:Ce nanoparticles was achieved. Oleic acid surface modification of the nanoparticles was verified by IR spectra. Quantum yields of LaF{sub 3}:Ce and OA-LaF{sub 3}:Ce nanoparticles were evaluated. Quantum yields of LaF{sub 3}:Ce are strongly dependent on OA surface modification. - Abstract: Cerium ions doped lanthanum fluoride (LaF{sub 3}:Ce) nanopowder as well as LaF{sub 3}:Ce nanopowder whose surfaces was modified by oleic acid (OA) were synthesized by using an in-situ hydrothermal process under the various doping concentrations. Based on the XRD spectra and TEM images, it was confirmed that the crystalline structured hexagonal LaF{sub 3}:Ce nanopowder was synthesized. Oleic acid was efficient for conversion of the water dispersible LaF{sub 3}:Ce nanoparticles to hydrophobic ones. Surface modification was verified by FTIR absorption spectrum as well as TEM images, showing no agglomeration between 5 and 10 nm scaled particles. Photoluminescence based on 5d ? 4f electronic transition of cerium ions excited at ?{sub ex} ?256 nm for both neat and OA encapsulated LaF{sub 3}:Ce nanoparticles decreases as the cerium concentration increases, while the quantum yields of OA encapsulated nanoparticles were much lower than the neat particles due to low photon transmittance of OA at the range longer than ?350 nm.

  5. Thermal Variation of Ce Valence in Mixed ValenceKondo Lattice Systems CeT2(Si1-xGex)2 with T= Mn and Ni

    SciTech Connect (OSTI)

    Liang,G.; Croft, M.

    2008-01-01

    The results on the thermal variation of Ce L3-valence in CeT2(Si1-xGex)2 series with 0{le}x{le}1 and T=Mn and Ni are reported. It is observed that for both series, the Ce valence increases with decreasing temperature and has little thermal variation for samples in the nearly trivalent regime. The magnitude of this thermal variation in the T=Mn series is much greater than in the T=Ni series. The results are explained by the degenerate Anderson model and correlated with the specific heat data.

  6. Interface Induced Carbonate Mineralization: A Fundamental Geochemical

    Office of Scientific and Technical Information (OSTI)

    Process Relevant to Carbon Sequestration (Technical Report) | SciTech Connect Interface Induced Carbonate Mineralization: A Fundamental Geochemical Process Relevant to Carbon Sequestration Citation Details In-Document Search Title: Interface Induced Carbonate Mineralization: A Fundamental Geochemical Process Relevant to Carbon Sequestration Mica, biotite, muscovite, diopside, tremolite, ultramafic rock, hematite, Ca-Mg-carbonate, calcite, aragonite, dolomite, crystal nucleation,

  7. Magnetic structure of the antiferromagnetic Kondo lattice compounds CeRhAl4Si2 and CeIrAl4Si2

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Ghimire, N. J.; Calder, S.; Janoschek, M.; Bauer, E. D.

    2015-06-01

    In this article, we have investigated the magnetic ground state of the antiferromagnetic Kondo-lattice compounds CeMAl4Si2(M = Rh, Ir) using neutron powder diffraction. Although both of these compounds show two magnetic transitions TN1 and TN2 in the bulk properties measurements, evidence for magnetic long-range order was only found below the lower transition TN2. Analysis of the diffraction profiles reveals a commensurate antiferromagnetic structure with a propagation vector k = (0, 0, 1/2). The magnetic moment in the ordered state of CeRhAl4Si2 and CeIrAl4Si2 were determined to be 1.14(2) and 1.41(3) μB/Ce, respectively, and are parallel to the crystallographic c-axis inmore » agreement with magnetic susceptibility measurements.« less

  8. Ternary ceramic alloys of Zr-Ce-Hf oxides

    DOE Patents [OSTI]

    Becher, P.F.; Funkenbusch, E.F.

    1990-11-20

    A ternary ceramic alloy is described which produces toughening of zirconia and zirconia composites through the stress transformation from tetragonal phase to monoclinic phase. This alloy, having the general formula Ce[sub x]Hf[sub y]Zr[sub 1[minus]x[minus]y]O[sub 2], is produced through the addition of appropriate amounts of ceria and hafnia to the zirconia. Typically, improved toughness is achieved with about 5 to about 15 mol % ceria and up to about 40 mol % hafnia. The preparation of alloys of these compositions are given together with data as to the densities, tetragonal phase content, hardness and fracture toughness. The alloys are useful in preparing zirconia bodies as well as reinforcing ceramic composites. 1 fig.

  9. Ternary ceramic alloys of ZR-CE-HF oxides

    DOE Patents [OSTI]

    Becher, Paul F. (Oak Ridge, TN); Funkenbusch, Eric F. (White Bear Lake, MN)

    1990-01-01

    A ternary ceramic alloy which produces toughening of zirconia and zirconia composites through the stress transformation from tetragonal phase to monoclinic phase. This alloy, having the general formula Ce.sub.x Hf.sub.y Zn.sub.1-x-y O.sub.2, is produced through the addition of appropriate amounts of ceria and hafnia to the zirconia. Typically, improved toughness is achieved with about 5 to about 15 mol % ceria and up to about 40 mol % hafnia. The preparation of alloys of these compositions are given together with data as to the densities, tetragonal phase content, hardness and fracture toughness. The alloys are useful in preparing zirconia bodies as well as reinforcing ceramic composites.

  10. Inelastic magnetic neutron scattering in CePd{sub 3}.

    SciTech Connect (OSTI)

    Lawrence, J. M.; Fanelli, V. R.; Goremychkin, E. A.; Osborn, R.; Bauer, E. D.; McClellan, K. J.; Christianson, A. D.; Univ. of California at Irvine; LANL; ORNL

    2008-01-01

    We have performed time-of-flight neutron scattering measurements on a single crystal of the intermediate valence compound CePd{sub 3}. At 10 K, a Kondo-esque inelastic magnetic scattering peak occurs near {Delta}E = 60 meV with maximum intensity for momentum transfer Q near the (1/2, 1/2, 0) zone boundary. Spectral weight is transferred to lower energy as Q varies until at zone center the intensity at 60 meV is considerably weaker. These results are in qualitative accord with predictions of the Anderson lattice. The Q-dependence may resolve an older controversy concerning the low-temperature scattering. We discuss the relationship of these results to our recent results in YbAl{sub 3}.

  11. Preparation and properties of ce-doped TiO{sub 2} photocatalyst

    SciTech Connect (OSTI)

    Yan, Ningning; Zhu, Zhongqi; Zhang, Jin; Zhao, Zongyan; Liu, Qingju

    2012-08-15

    Highlights: ? The cerium ion doped TiO{sub 2} (Ce-TiO{sub 2}) powders were prepared and characterized. ? The spectrum absorption region of Ce-TiO{sub 2} is red-shifted to visible light. ? The recombination of photo-generated electron-hole pairs of Ce-TiO{sub 2} is inhibited. ? The photocatalytic activity was effected by Ce ion content and greatly improved. -- Abstract: TiO{sub 2} nanoparticles doped with different content of Ce ion were prepared by solgel method. The samples were characterized by XRD, XPS, TEM, UVVis, and PL, the photocatalytic activity was evaluated by photocatalytic degradation of methylene blue (MB) under the irradiation of fluorescent lamp. The results indicate that Ce ion is incorporated into the lattice of TiO{sub 2}, which can restrain the increase of grain size, broaden the absorption region to visible light, and inhibit the recombination of the photo-generated electron and hole pairs. Moreover, the photocatalytic activity of Ce-TiO{sub 2} in MB degradation is evidently enhanced. The MB degradation rate of the sample with Ce:Ti = 0.33% (molar ratio) in 8 h is 90.03%, which is much higher than that of P25 (68.19%).

  12. CO Oxidation at the Interface of Au Nanoclusters and the Stepped-CeO2(111) Surface

    SciTech Connect (OSTI)

    Kim H. Y.; Henkelman, G.

    2013-01-14

    To reveal the richer chemistry of CO oxidation by CeO2 supported Au Nanoclusters NCs)/Nanoparticles, we design a Au12 supported on a stepped-CeO2 model (Au/CeO2-step) and study various kinds of CO oxidation mechanisms at the interface of the Au/CeO2-step: oxygen spillover from the CeO2 to the Au NCs;2 CO oxidation by the O2 bound to the Au-Ce3+ interface;3 and CO oxidation by the Mars-van Krevelen (M-vK) mechanism.4 DFT+U calculations show that lattice oxygen at the CeO2 step edge oxidizes CO bound to Au NCs by the M-vK mechanism. CO2 desorption determines the rate of CO oxidation and the vacancy formation energy (Evac) is a reactivity descriptor for CO oxidation. The maximum Evac that insures spontaneous CO2 production is higher for the Au/CeO2-step than the Au/CeO2-surface suggesting that the CeO2-step is a better supporting material than the CeO2-surface for CO oxidation by the Au/CeO2. Our results also suggest that for CO oxidation by Au NCs supported on nano- or meso-structured CeO2, which is the case of industrial catalysts, the M-vK mechanism accounts for a large portion of the total activity.

  13. Mineral Selection for Multicomponent Equilibrium Geothermometry

    SciTech Connect (OSTI)

    Plamer, C. D.; Ohly, S. R.; Smith, R. W.; Neupane, G.; McLing, T.; Mattson, E.

    2015-04-01

    Multicomponent geothermometry requires knowledge of the mineral phases in the reservoir with which the geothermal fluids may be equilibrated. These minerals phases are most often alteration products rather than primary minerals. We have reviewed the literature on geothermal systems representing most major geologic environments typically associated with geothermal activity and identified potential alteration products in various environments. We have included this information in RTEst, a code we have developed to estimate reservoir conditions (temperature, CO2 fugacity) from the geochemistry of near-surface geothermal waters. The information has been included in RTEst through the addition of filters that decrease the potential number of minerals from all possibilities based on the basis species to those that are more relevant to the particular conditions in which the user is interested. The three groups of filters include host rock type (tholeiitic, calc-alkaline, silicic, siliciclastic, carbonate), water type (acidic, neutral), and the temperature range over which the alteration minerals were formed (low, medium, high). The user-chosen mineral assemblage is checked to make sure that it does not violate the Gibbs phase rule. The user can select one of three mineral saturation weighting schemes that decrease the chance the optimization from being skewed by reaction stoichiometry or analytical uncertainty.

  14. Mineral Selection for Multicomponent Equilibrium Geothermometry

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Plamer, C. D.; Ohly, S. R.; Smith, R. W.; Neupane, G.; McLing, T.; Mattson, E.

    2015-04-01

    Multicomponent geothermometry requires knowledge of the mineral phases in the reservoir with which the geothermal fluids may be equilibrated. These minerals phases are most often alteration products rather than primary minerals. We have reviewed the literature on geothermal systems representing most major geologic environments typically associated with geothermal activity and identified potential alteration products in various environments. We have included this information in RTEst, a code we have developed to estimate reservoir conditions (temperature, CO2 fugacity) from the geochemistry of near-surface geothermal waters. The information has been included in RTEst through the addition of filters that decrease the potential numbermore » of minerals from all possibilities based on the basis species to those that are more relevant to the particular conditions in which the user is interested. The three groups of filters include host rock type (tholeiitic, calc-alkaline, silicic, siliciclastic, carbonate), water type (acidic, neutral), and the temperature range over which the alteration minerals were formed (low, medium, high). The user-chosen mineral assemblage is checked to make sure that it does not violate the Gibbs phase rule. The user can select one of three mineral saturation weighting schemes that decrease the chance the optimization from being skewed by reaction stoichiometry or analytical uncertainty.« less

  15. Process for the physical segregation of minerals

    DOE Patents [OSTI]

    Yingling, Jon C.; Ganguli, Rajive

    2004-01-06

    With highly heterogeneous groups or streams of minerals, physical segregation using online quality measurements is an economically important first stage of the mineral beneficiation process. Segregation enables high quality fractions of the stream to bypass processing, such as cleaning operations, thereby reducing the associated costs and avoiding the yield losses inherent in any downstream separation process. The present invention includes various methods for reliably segregating a mineral stream into at least one fraction meeting desired quality specifications while at the same time maximizing yield of that fraction.

  16. Division of Energy and Mineral Resources Management - Projects

    Office of Environmental Management (EM)

    BIA - - Division of Energy and Mineral Division of Energy and Mineral Resources Management Resources Management 1 1 Assistant Secretary Assistant Secretary - - Indian Affairs Indian Affairs Office of Indian Office of Indian Energy and Economic Energy and Economic Development Development Division of Energy and Division of Energy and Mineral Resources Mineral Resources Management Management BIA BIA - - Division of Energy and Mineral Division of Energy and Mineral Resources Management Resources

  17. Bashfords Hot Mineral Spa Pool & Spa Low Temperature Geothermal...

    Open Energy Info (EERE)

    Bashfords Hot Mineral Spa Pool & Spa Low Temperature Geothermal Facility Jump to: navigation, search Name Bashfords Hot Mineral Spa Pool & Spa Low Temperature Geothermal Facility...

  18. Mineral Recovery Creates Revenue Stream for Geothermal Energy...

    Energy Savers [EERE]

    Mineral Recovery Creates Revenue Stream for Geothermal Energy Development Mineral Recovery Creates Revenue Stream for Geothermal Energy Development December 1, 2015 - 8:00am...

  19. Mineral Leasing Act for Acquired Lands of 1947 | Open Energy...

    Open Energy Info (EERE)

    of the Mineral Leasing Act and the authority of the Secretary of the Interior over oil and gas operations to federal "acquired lands." References Mineral Leasing Act for...

  20. ITP Mining: Mining Industry of the Future Mineral Processing...

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    of the Future Mineral Processing Technology Roadmap ITP Mining: Mining Industry of the Future Mineral Processing Technology Roadmap PDF icon mptroadmap.pdf More Documents & ...

  1. Buckhorn Mineral Wells Pool & Spa Low Temperature Geothermal...

    Open Energy Info (EERE)

    Buckhorn Mineral Wells Pool & Spa Low Temperature Geothermal Facility Jump to: navigation, search Name Buckhorn Mineral Wells Pool & Spa Low Temperature Geothermal Facility...

  2. Indian Mineral Leasing Act of 1938 | Open Energy Information

    Open Energy Info (EERE)

    Provides for leasing of minerals on tribal lands References IMLA1 United States v. Navajo Nation2 The Indian Mineral Leasing Act of 1938 (IMLA) provides that "unallotted...

  3. Vietnam National Coal Mineral Industries Group Vinacomin | Open...

    Open Energy Info (EERE)

    National Coal Mineral Industries Group Vinacomin Jump to: navigation, search Name: Vietnam National Coal-Mineral Industries Group (Vinacomin) Place: Vietnam Product: Vietnam-based...

  4. Geology and Mineral Deposits of Churchill County, Nevada | Open...

    Open Energy Info (EERE)

    Mineral Deposits of Churchill County, Nevada Jump to: navigation, search OpenEI Reference LibraryAdd to library Report: Geology and Mineral Deposits of Churchill County, Nevada...

  5. H. R. S. 182 - Reservation and Disposition of Government Mineral...

    Open Energy Info (EERE)

    Mineral Rights (2012). Retrieved from "http:en.openei.orgwindex.php?titleH.R.S.182-ReservationandDispositionofGovernmentMineralRights&oldid801574" ...

  6. Relations Of Ammonium Minerals At Several Hydrothermal Systems...

    Open Energy Info (EERE)

    to mineralization. Submicroscopic analysis of ammonium minerals from two mercury- and gold-bearing hot-springs deposits at Ivanhoe, Nevada and McLaughlin, California shows that...

  7. Studies on Ca2+-Doped CeBr3 Scintillating Materials

    SciTech Connect (OSTI)

    Guss, P. [NSTec; Foster, M. E. [SNL; Wong, B. M. [SNL; Doty, F. P. [SNL; Shah, K. [RMD; Squillante, M. [RMD; Glodo, J. [RMD; Yuan, D. [NSTec

    2013-07-03

    Despite the outstanding scintillation performance characteristics of cerium tribromide (CeBr3) and cerium-activated lanthanum tribromide (LaBr3:Ce), their commercial availability and application is limited due to the difficulties of growing large, crack-free single crystals from these fragile materials. The objective of this investigation was to employ aliovalent doping to increase crystal strength while maintaining the optical properties of the crystal. One divalent dopant (Ca2+) was investigated as a dopant to strengthen CeBr3 without negatively impacting scintillation performance. Ingots containing nominal concentrations of 1.9% of the Ca2+ dopant were grown. Preliminary scintillation measurements are presented for this aliovalently doped scintillator. Ca2+-doped CeBr3 exhibited little or no change in the peak fluorescence emission for 371 nm optical excitation for CeBr3. The structural, electronic, and optical properties of CeBr3 crystals were investigated using the density functional theory within generalized gradient approximation. The calculated lattice parameters are in good agreement with the experimental data. The energy band structures and density of states were obtained. The optical properties of CeBr3, including the dielectric function, were calculated.

  8. Recovery of minerals from US coals

    SciTech Connect (OSTI)

    Vanderborgh, N.E.

    1982-01-01

    Projections show that domestic coal will serve for the majority of energy supplies during the next decades. Thorough chemical cleaning of this coal can be accomplished in long residence time, slurry transport systems to produce high-quality fuel product. Concurrently, mineral recovery from coals will supplement existing ores. This paper describes this concept and given preliminary engineering considerations for mineral recovery during transport operations.

  9. Dissolving the mineral calcite | Argonne National Laboratory

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    calcite Share Topic Programs Chemical sciences & engineering Synchrotron radiation X-ray imaging & holography Argonne's X-ray Reflection Interfacial Microscope allows researchers to observe mineral surfaces. Powered by the Advanced Photon Source, the microscope allows researchers to "see" the surface structure in real time as "etch pits," or surface holes, developed on the mineral calcite

  10. Division of Energy and Mineral Development

    Office of Environmental Management (EM)

    Office of Indian Energy and Economic Development Division of Energy and Mineral Development DOE Energy Efficiency & Renewable Energy Tribal Energy Program November 14 th , 2011 Winter Jojola-Talburt, Electrical Engineer Assistant Secretary - Indian Affairs (Larry Echo Hawk) Director Bureau of Indian Affairs Director Bureau of Indian Education Deputy Assistant Secretary Policy and Economic Development (Jodi Gillette) Division of Energy and Mineral Development Division of Economic Development

  11. Neutron scattering of CeNi at the SNS-ORNL: A preliminary report

    Office of Scientific and Technical Information (OSTI)

    (Conference) | SciTech Connect Conference: Neutron scattering of CeNi at the SNS-ORNL: A preliminary report Citation Details In-Document Search Title: Neutron scattering of CeNi at the SNS-ORNL: A preliminary report This is a preliminary report of a neutron scattering experiment used to investigate 4f electron behavior in Ce. Authors: Mirmelstein, A. [1] ; Podlesnyak, Andrey A [2] ; Kolesnikov, Alexander I [2] ; Saporov, B. [3] ; Sefat, A.S. [3] ; Tobin, J. G. [4] + Show Author Affiliations

  12. Magnitude of the magnetic exchange interaction in the heavy-fermion antiferromagnet CeRhIn?

    SciTech Connect (OSTI)

    Das, Pinaki [Los Alamos National Laboratory (LANL), Los Alamos, NM (United States); Lin, S. -Z. [Los Alamos National Laboratory (LANL), Los Alamos, NM (United States); Ghimire, N.? J. [Los Alamos National Laboratory (LANL), Los Alamos, NM (United States); Huang, K. [Los Alamos National Laboratory (LANL), Los Alamos, NM (United States); Univ. of California, San Diego, La Jolla, CA (United States); Ronning, F. [Los Alamos National Laboratory (LANL), Los Alamos, NM (United States); Bauer, E.? D. [Los Alamos National Laboratory (LANL), Los Alamos, NM (United States); Thompson, J.? D. [Los Alamos National Laboratory (LANL), Los Alamos, NM (United States); Batista, C.? D. [Los Alamos National Laboratory (LANL), Los Alamos, NM (United States); Ehlers, G. [Oak Ridge National Lab. (ORNL), Oak Ridge, TN (United States); Janoschek, M. [Los Alamos National Laboratory (LANL), Los Alamos, NM (United States)

    2014-12-01

    We have used high-resolution neutron spectroscopy experiments to determine the complete spin wave spectrum of the heavy-fermion antiferromagnet CeRhIn?. The spin wave dispersion can be quantitatively reproduced with a simple frustrated J??J? model that also naturally explains the magnetic spin-spiral ground state of CeRhIn? and yields a dominant in-plane nearest-neighbor magnetic exchange constant J?=0.74(3)??meV. Our results pave the way to a quantitative understanding of the rich low-temperature phase diagram of the prominent CeTIn? (T = Co, Rh, Ir) class of heavy-fermion materials.

  13. Electronic Band Dispersion Of CeAg{sub 2}Ge{sub 2} Studied Using Angle

    Office of Scientific and Technical Information (OSTI)

    Resolved Photoemission Spectroscopy (Journal Article) | SciTech Connect Electronic Band Dispersion Of CeAg{sub 2}Ge{sub 2} Studied Using Angle Resolved Photoemission Spectroscopy Citation Details In-Document Search Title: Electronic Band Dispersion Of CeAg{sub 2}Ge{sub 2} Studied Using Angle Resolved Photoemission Spectroscopy Angle resolved photoelectron spectroscopy has been used to determine the electronic band dispersion of CeAg{sub 2}Ge{sub 2} single crystal along the {Gamma}-Z

  14. SEMI-ANNUAL REPORTS FOR CE FLNG, LLC (CAMBRIDGE) - DK. NO. 12-123-LNG -

    Energy Savers [EERE]

    ORDER 3193 | Department of Energy CE FLNG, LLC (CAMBRIDGE) - DK. NO. 12-123-LNG - ORDER 3193 SEMI-ANNUAL REPORTS FOR CE FLNG, LLC (CAMBRIDGE) - DK. NO. 12-123-LNG - ORDER 3193 PDF icon April 2013 PDF icon October 2013 PDF icon April 2014 PDF icon October 2014 PDF icon April 2015 PDF icon October 2015 More Documents & Publications CE FLNG, LLC - FE DKT. NO. 12-123-LNG - ORDER 3193 EIS-0497: Notice of Intent to Prepare an Environmental Impact Statement SEMI-ANNUAL REPORTS FOR FREEPORT LNG

  15. Lattice instabilities in heavy fermion superconductors. [CeCu/sub 2/Si/sub 2/; CeAl/sub 3/; CeCu/sub 6/; UBe/sub 13/; UPt/sub 3/

    SciTech Connect (OSTI)

    Wohlleben, D.

    1987-01-01

    This paper shows that while in nonsuperconducting HF systems such as CeCu/sub 6/, CeAl/sub 3/ and stoichiometric CeCu/sub 2/Si/sub 2/, the large electronic ..gamma.. is due to a very narrow f band, in the three HF superconductors UBe/sub 13/, UPt/sub 3/ and nonstochiometric CeCu/sub 2/Si/sub 2/, it is not. The f band of these systems, as measured by their response to magnetic fields in three different ways, is much wider than suggested by the large ..gamma... According to their actual f band width, the HF superconductors belong into the Bantam Fermion class. It is argued that most of the large ..gamma.. of the HF superconductors is not of electronic origin and that it is instead caused by the precursor of a martensitic phase transition of the lattice or by a crystallographic phase mixture, i.e., that it is due to the displacive degrees of freedom. This suggests that the superconductivity of all three HF superconductors is caused by some special, low energy phonons rather than by a narrow f band. 52 refs., 4 figs., 3 tabs.

  16. A comparison of the structure and localized magnetism in Ce{sub 2}PdGa{sub 12} with the heavy fermion CePdGa{sub 6}

    SciTech Connect (OSTI)

    Macaluso, Robin T. [Department of Chemistry, Louisiana State University, Baton Rouge, LA 70803 (United States); Millican, Jasmine N. [Department of Chemistry, Louisiana State University, Baton Rouge, LA 70803 (United States); Nakatsuji, Satoru [Department of Physics, Kyoto University, Kyoto, Japan 606-8502 (Japan); Lee, Han-Oh [Department of Physics, University of California, Davis, CA 95616 (United States); Carter, B. [Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Moreno, Nelson O. [Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Fisk, Zachary [Department of Physics, University of California, Davis, CA 95616 (United States); Chan, Julia Y. [Department of Chemistry, Louisiana State University, Baton Rouge, LA 70803 (United States)]. E-mail: jchan@lsu.edu

    2005-11-15

    Single crystals of Ce{sub 2}PdGa{sub 12} have been synthesized in Ga flux and characterized by X-ray diffraction. This compound crystallizes in the tetragonal P4/nbm space group, Z=2 with lattice parameters of a=6.1040(2)A and c=15.5490(6)A. It shows strongly anisotropic magnetism and orders antiferromagnetically at T{sub N}{approx}11K. A field-induced metamagnetic transition to the ferromagnetic state is observed below T{sub N}. Structure-property relationships with the related heavy-fermion antiferromagnet CePdGa{sub 6} are discussed.

  17. ASKO Appliances: Order (2012-CE-19/2004) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    (2012-CE-192004) July 20, 2012 DOE ordered ASKO Appliances, Inc. to pay a 36,500 civil penalty after finding ASKO had failed to certify that certain models of residential...

  18. Pressure-Induced Structural Phase Transition in CeNi: X-ray and...

    Office of Scientific and Technical Information (OSTI)

    Journal Article: Pressure-Induced Structural Phase Transition in CeNi: X-ray and Neutron Scattering Studies and First-Principles Calculations Citation Details In-Document Search...

  19. Neutron Scattering of CeNi at the Spallation Neutron Source at...

    Office of Scientific and Technical Information (OSTI)

    Title: Neutron Scattering of CeNi at the Spallation Neutron Source at Oak Ridge National Laboratory: A Preliminary Report Authors: Tobin, J G ; Mirmelstein, A V ; Podlesnyak, A ; ...

  20. f-electron correlations in nonmagnetic Ce studied by means of...

    Office of Scientific and Technical Information (OSTI)

    f-electron correlations in nonmagnetic Ce studied by means of spin-resolved resonant photoemission Citation Details In-Document Search Title: f-electron correlations in nonmagnetic ...

  1. MINER{nu}A Test Beam Commissioning

    SciTech Connect (OSTI)

    Higuera, A.; Castorena, J.; Urrutia, Z.; Felix, J.; Zavala, G.

    2009-12-17

    MINER{nu}A Main INjector ExpeRiment {nu}-A is a high-statistic neutrino scattering experiment that will ran in the NuMI Beam Hall at Fermilab. To calibrate the energy response of the MINER{nu}A detector, a beamline is being designed for the MINER{nu}A Test Beam Detector (TBD). The TBD is a replica of the full MINER{nu}A detector at small scale for calibration studies of the main detector. The beamline design consists of the following parts: a copper target, used to generate tertiaries from an incoming secondary beam; a steel collimator for tertiaries, which also serves as a dump for the incoming beam; a time of fight system (scintillator planes); four wire chambers, for angle measurements and tracking; and two dipole magnets, used as an spectrometer. During last October, the first commissioning run of the MINER{nu}A Test Beam took place in the Meson Test Beam Facility at Fermilab. We commissioned the target and collimator of the new tertiary beamline.

  2. Pressure-Induced Structural Phase Transition in CeNi: X-ray and Neutron

    Office of Scientific and Technical Information (OSTI)

    Scattering Studies and First-Principles Calculations (Journal Article) | SciTech Connect Journal Article: Pressure-Induced Structural Phase Transition in CeNi: X-ray and Neutron Scattering Studies and First-Principles Calculations Citation Details In-Document Search This content will become publicly available on August 3, 2016 Title: Pressure-Induced Structural Phase Transition in CeNi: X-ray and Neutron Scattering Studies and First-Principles Calculations The pressure-induced structural

  3. Results for aliovalent doping of CeBr{sub 3} with Ca{sup 2+}

    SciTech Connect (OSTI)

    Guss, Paul; Foster, Michael E.; Wong, Bryan M.; Patrick Doty, F.; Shah, Kanai; Squillante, Michael R.; Shirwadkar, Urmila; Hawrami, Rastgo; Tower, Joshua; Yuan, Ding

    2014-01-21

    Despite the outstanding scintillation performance characteristics of cerium tribromide (CeBr{sub 3}) and cerium-activated lanthanum tribromide, their commercial availability and application are limited due to the difficulties of growing large, crack-free single crystals from these fragile materials. This investigation employed aliovalent doping to increase crystal strength while maintaining the optical properties of the crystal. One divalent dopant (Ca{sup 2+}) was used as a dopant to strengthen CeBr{sub 3} without negatively impacting scintillation performance. Ingots containing nominal concentrations of 1.9% of the Ca{sup 2+} dopant were grown, i.e., 1.9% of the CeBr{sub 3} molecules were replaced by CaBr{sub 2} molecules, to match our target replacement of 1 out of 54 cerium atoms be replaced by a calcium atom. Precisely the mixture was composed of 2.26 g of CaBr{sub 2} added to 222.14 g of CeBr{sub 3}. Preliminary scintillation measurements are presented for this aliovalently doped scintillator. Ca{sup 2+}-doped CeBr{sub 3} exhibited little or no change in the peak fluorescence emission for 371?nm optical excitation for CeBr{sub 3}. The structural, electronic, and optical properties of CeBr{sub 3} crystals were studied using the density functional theory within the generalized gradient approximation. Calculated lattice parameters are in agreement with the experimental data. The energy band structures and density of states were obtained. The optical properties of CeBr{sub 3}, including the dielectric function, were calculated.

  4. ASKO Appliances: Order (2012-CE-19/2004) | Department of Energy

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    ASKO Appliances: Order (2012-CE-19/2004) ASKO Appliances: Order (2012-CE-19/2004) July 20, 2012 DOE ordered ASKO Appliances, Inc. to pay a $36,500 civil penalty after finding ASKO had failed to certify that certain models of residential dishwashers and clothes washers comply with the applicable energy and water conservation standards. DOE assessed a higher civil penalty due to a prior history of the same type of violation. The Order adopted a Compromise Agreement, which reflected settlement

  5. f-electron correlations in nonmagnetic Ce studied by means of spin-resolved

    Office of Scientific and Technical Information (OSTI)

    resonant photoemission (Journal Article) | SciTech Connect f-electron correlations in nonmagnetic Ce studied by means of spin-resolved resonant photoemission Citation Details In-Document Search Title: f-electron correlations in nonmagnetic Ce studied by means of spin-resolved resonant photoemission Authors: Yu, S. -W. ; Komesu, T. ; Chung, B. W. ; Waddill, G. D. ; Morton, S. A. ; Tobin, J. G. [1] ; MUST) [2] + Show Author Affiliations LLNL ( Publication Date: 2015-10-15 OSTI Identifier:

  6. Mitsubishi Electric: Consent Decree (2011-CE-01/0202) | Department of

    Office of Environmental Management (EM)

    Energy Mitsubishi Electric: Consent Decree (2011-CE-01/0202) Mitsubishi Electric: Consent Decree (2011-CE-01/0202) May 7, 2010 In this consent degree, the Air-Conditioning, Heating and Refrigeration Institute (AHRI) agrees to pay $5,000 on behalf of Mitsubishi Electric & Electronics, USA, Inc. Mitsubishi Electric agreed that the required certification reports were not filed with DOE; however, Mitsubishi had an agreement with AHRI for AHRI to submit those reports on Mitsubishi's behalf.

  7. Antiferromagnetic ordering in the doped Kondo insulator CeRhSb

    SciTech Connect (OSTI)

    Menon, L.; Malik, S.K.

    1997-06-01

    CeRhSb, the so-called {open_quotes}Kondo insulator,{close_quotes} is a mixed-valent compound showing a gap formation in the electronic density of states. On the other hand, CePdSb is ferromagnetically ordered with a Curie temperature of {approximately}17 K. We have carried out magnetic susceptibility and electrical resistivity measurements on CeRh{sub 1{minus}x}Pd{sub x}Sb (0{le}x{le}1.0), to study the ground-state properties of this system. For small Pd doping in CeRhSb, up to 20{percent}, the gap continually diminishes and no magnetic ordering is observed down to 2 K. In the region 0.3{le}x{le}0.4, as soon as the gap is suppressed, an antiferromagnetic ground state is observed. In the region 0.5{le}x{lt}0.7, the compounds are not single phase. At the CePdSb end, in the region 0.7{le}x{le}1, the ground state is ferromagnetic. The observation of an antiferromagnetic phase in the phase diagram of CeRh{sub 1{minus}x}Pd{sub x}Sb, where neither end is antiferromagnetic, is interesting and is discussed in the light of some recent theoretical models. {copyright} {ital 1997} {ital The American Physical Society}

  8. Structure and scintillation yield of Ce-doped AlGa substituted yttrium garnet

    SciTech Connect (OSTI)

    Sidletskiy, Oleg; Kononets, Valerii; Lebbou, Kheirreddine; Neicheva, Svetlana; Voloshina, Olesya; Bondar, Valerii; Baumer, Vyacheslav; Belikov, Konstantin; Gektin, Alexander; Grinyov, Boris; Joubert, Marie-France

    2012-11-15

    Highlights: ? Range of Y{sub 3}(Al{sub 1?x}Ga{sub x}){sub 5}O{sub 12}:Ce solid solution crystals are grown from melt by the Czochralski method. ? Light yield of mixed crystals reaches 130% of the YAG:Ce value at x ? 0.4. ? ?1% of antisite defects is formed in YGG:Ce, but no evidence of this is obtained for the rest of crystals. -- Abstract: Structure and scintillation yield of Y{sub 3}(Al{sub 1?x}Ga{sub x}){sub 5}O{sub 12}:Ce solid solution crystals are studied. Crystals are grown from melt by the Czochralski method. Distribution of host cations in crystal lattice is determined. Quantity of antisite defects in crystals is evaluated using XRD and atomic emission spectroscopy data. Trend of light output at Al/Ga substitution in Y{sub 3}(Al{sub 1?x}Ga{sub x}){sub 5}O{sub 12}:Ce is determined for the first time. Light output in mixed crystals reaches 130% comparative to Ce-doped yttriumaluminum garnet. Luminescence properties at Al/Ga substitution are evaluated.

  9. An Update on Improvements to NiCE Support for RELAP-7

    SciTech Connect (OSTI)

    McCaskey, Alex; Wojtowicz, Anna; Deyton, Jordan H.; Patterson, Taylor C.; Billings, Jay Jay

    2015-01-01

    The Multiphysics Object-Oriented Simulation Environment (MOOSE) is a framework that facilitates the development of applications that rely on finite-element analysis to solve a coupled, nonlinear system of partial differential equations. RELAP-7 represents an update to the venerable RELAP-5 simulator that is built upon this framework and attempts to model the balance-of-plant concerns in a full nuclear plant. This report details the continued support and integration of RELAP-7 and the NEAMS Integrated Computational Environment (NiCE). RELAP-7 is fully supported by the NiCE due to on-going work to tightly integrate NiCE with the MOOSE framework, and subsequently the applications built upon it. NiCE development throughout the first quarter of FY15 has focused on improvements, bug fixes, and feature additions to existing MOOSE-based application support. Specifically, this report will focus on improvements to the NiCE MOOSE Model Builder, the MOOSE application job launcher, and the 3D Nuclear Plant Viewer. This report also includes a comprehensive tutorial that guides RELAP-7 users through the basic NiCE workflow: from input generation and 3D Plant modeling, to massively parallel job launch and post-simulation data visualization.

  10. Iron oxyhydroxide mineralization on microbial extracellular polysaccharides

    SciTech Connect (OSTI)

    Chan, Clara S.; Fakra, Sirine C.; Edwards, David C.; Emerson, David; Banfield, Jillian F.

    2010-06-22

    Iron biominerals can form in neutral pH microaerophilic environments where microbes both catalyze iron oxidation and create polymers that localize mineral precipitation. In order to classify the microbial polymers that influence FeOOH mineralogy, we studied the organic and mineral components of biominerals using scanning transmission X-ray microscopy (STXM), micro X-ray fluorescence ({mu}XRF) microscopy, and high-resolution transmission electron microscopy (HRTEM). We focused on iron microbial mat samples from a creek and abandoned mine; these samples are dominated by iron oxyhydroxide-coated structures with sheath, stalk, and filament morphologies. In addition, we characterized the mineralized products of an iron-oxidizing, stalk-forming bacterial culture isolated from the mine. In both natural and cultured samples, microbial polymers were found to be acidic polysaccharides with carboxyl functional groups, strongly spatially correlated with iron oxyhydroxide distribution patterns. Organic fibrils collect FeOOH and control its recrystallization, in some cases resulting in oriented crystals with high aspect ratios. The impact of polymers is particularly pronounced as the materials age. Synthesis experiments designed to mimic the biomineralization processes show that the polysaccharide carboxyl groups bind dissolved iron strongly but release it as mineralization proceeds. Our results suggest that carboxyl groups of acidic polysaccharides are produced by different microorganisms to create a wide range of iron oxyhydroxide biomineral structures. The intimate and potentially long-term association controls the crystal growth, phase, and reactivity of iron oxyhydroxide nanoparticles in natural systems.

  11. Ionic liquid-assisted sonochemical preparation of CeO2 nanoparticles for CO oxidation

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Alammar, Tarek; Noei, Heshmat; Wang, Yuemin; Grünert, Wolfgang; Mudring, Anja -Verena

    2014-10-10

    CeO2 nanoparticles were synthesized via a one-step ultrasound synthesis in different kinds of ionic liquids based on bis(trifluoromethanesulfonylamide, [Tf2N]–, in combination with various cations including 1-butyl-3-methylimidazolium ([C4mim]+), 1-ethyl-2,3-dimethylimidazolium ([Edimim]+), butyl-pyridinium([Py4]+), 1-butyl-1-methyl-pyrrolidinium ([Pyrr14]+), and 2-hydroxyethyl-trimethylammonium ([N1112OH]+). Depending on synthetic parameters, such as ionic liquid, Ce(IV) precursor, heating method, and precipitator, formed ceria exhibits different morphologies, varying from nanospheres, nanorods, nanoribbons, and nanoflowers. The morphology, crystallinity, and chemical composition of the obtained materials were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), energy dispersive X-ray spectroscopy (EDX), Raman spectroscopy, and N2 adsorption. The structural and electronic propertiesmore » of the as-prepared CeO2 samples were probed by CO adsorption using IR spectroscopy under ultrahigh vacuum conditions. The catalytic activities of CeO2 nanoparticles were investigated in the oxidation of CO. CeO2 nanospheres obtained sonochemically in [C4mim][Tf2N] exhibit the best performance for low-temperature CO oxidation. As a result, the superior catalytic performance of this material can be related to its mesoporous structure, small particle size, large surface area, and high number of surface oxygen vacancy sites.« less

  12. Reduced graphene oxide/CeO{sub 2} nanocomposite with enhanced photocatalytic performance

    SciTech Connect (OSTI)

    Kaur, Jasmeet Anand, Kanika; Singh, Gurpreet; Hastir, Anita; Virpal,; Singh, Ravi Chand; Anand, Kanica

    2015-05-15

    In this work, reduced graphene oxide /cerium oxide (RGO/CeO{sub 2}) nanocomposite was synthesized by in situ reduction of cerium nitrate Ce(NO{sub 3}){sub 3}6H{sub 2}O in the presence of graphene oxide by hydrazine hydrate (N{sub 2}H{sub 4}.H{sub 2}O). The intrinsic characteristics of as-prepared nanocomposite were studied using powder x-ray diffraction (XRD), Raman spectroscopy and field-emission scanning electron microscopy (FESEM). The photocatalytic degradation of methylene blue (MB) was employed as a model reaction to evaluate the photocatalytic activity of the RGO/CeO{sub 2} nanocomposite. The as-obtained RGO/CeO{sub 2} nanocomposite displays a significantly enhanced photocatalytic degradation of MB dye in comparison with bare CeO{sub 2} nanoparticles under sunlight irradiation, which can be attributed to the improved separation of electron-hole pairs and enhanced adsorption performance due to presence of RGO.

  13. Structural and magnetic phase transitions in CeCu6-xTx (T = Ag,Pd)

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Poudel, Lekhanath N.; De la cruz, Clarina; Payzant, E. Andrew; Koehler, Michael R.; May, Andrew F.; Garlea, Vasile O.; Taylor, Alice E.; Parker, David S.; Cao, Huibo B.; McGuire, Michael A.; et al

    2015-12-15

    The structural and the magnetic properties of CeCu6-xAgx (0 ≤ x ≤ 0.85) and CeCu6-xPdx (0 ≤ x ≤ 0.4) have been studied using neutron diffraction, resonant ultrasound spectroscopy (RUS), x-ray diffraction measurements, and first principles calculations. The structural and magnetic phase diagrams of CeCu6-xAgx and CeCu6-xPdx as a function of Ag/Pd composition are reported. The end member, CeCu6, undergoes a structural phase transition from an orthorhombic (Pnma) to a monoclinic (P21/c) phase at 240 K. In CeCu6-xAgx, the structural phase transition temperature (Ts) decreases linearly with Ag concentration and extrapolates to zero at xS ≈ 0.1. The structural transitionmore » in CeCu6-xPdx remains unperturbed with Pd substitution within the range of our study. The lattice constant b slightly decreases with Ag/Pd doping, whereas a and c increase with an overall increase in the unit cell volume. Both systems, CeCu6-xAgx and CeCu6-xPdx, exhibit a magnetic quantum critical point (QCP), at x ≈ 0.2 and x ≈ 0.05, respectively. Near the QCP, long range antiferromagnetic ordering takes place at an incommensurate wave vector (δ1 0 δ2), where δ1 ~ 0.62, δ2 ~ 0.25, x = 0.125 for CeCu6-xPdx and δ1 ~ 0.64, δ2 ~ 0.3, x = 0.3 for CeCu6-xAgx. As a result, the magnetic structure consists of an amplitude modulation of the Ce moments which are aligned along the c axis of the orthorhombic unit cell.« less

  14. Molecular Characterization of Bacterial Respiration on Minerals

    SciTech Connect (OSTI)

    Blake, Robert C.

    2013-04-26

    The overall aim of this project was to contribute to our fundamental understanding of proteins and biological processes under extreme environmental conditions. We sought to define the biochemical and physiological mechanisms that underlie biodegradative and other cellular processes in normal, extreme, and engineered environments. Toward that end, we sought to understand the substrate oxidation pathways, the electron transport mechanisms, and the modes of energy conservation employed during respiration by bacteria on soluble iron and insoluble sulfide minerals. In accordance with these general aims, the specific aims were two-fold: To identify, separate, and characterize the extracellular biomolecules necessary for aerobic respiration on iron under strongly acidic conditions; and to elucidate the molecular principles whereby these bacteria recognize and adhere to their insoluble mineral substrates under harsh environmental conditions. The results of these studies were described in a total of nineteen manuscripts. Highlights include the following: 1. The complete genome of Acidithiobacillus ferrooxidans ATCC 23270 (type strain) was sequenced in collaboration with the DOE Joint Genome Institute; 2. Genomic and mass spectrometry-based proteomic methods were used to evaluate gene expression and in situ microbial activity in a low-complexity natural acid mine drainage microbial biofilm community. This was the first effort to successfully analyze a natural community using these techniques; 3. Detailed functional and structural studies were conducted on rusticyanin, an acid-stable electron transfer protein purified from cell-free extracts of At. ferrooxidans. The three-dimensional structure of reduced rusticyanin was determined from a combination of homonuclear proton and heteronuclear 15N- and 13C-edited NMR spectra. Concomitantly, the three-dimensional structure of oxidized rusticyanin was determined by X-ray crystallography to a resolution of 1.9 A by multiwavelength anomalous dispersion (MAD) phasing; 4. An acid-stable red cytochrome with a novel absorbance peak at 579 nm was purified from cell-free extracts of L. ferriphilum. Functional studies demonstrated that this cytochrome was an important component of the aerobic iron respiratory chain in this organism; 5. The specific adhesion of At. ferrooxidans to pyrite is mediated by an extracellular protein that was identified as aporusticyanin. The adhesion of At. ferrooxidans to minerals was characterized by high affinity binding that exhibited a high specificity for pyrite over other sulfide minerals. The principal biopolymer involved in this high-affinity adhesion to pyrite was isolated by mineral affinity chromatography and identified as aporusticyanin. The adhesion of purified aporusticyanin to minerals was observed to adhere to different mineral with a pattern of reactivity identical to that observed with the intact bacterium. Further, preincubation of pyrite with excess exogenous aporusticyanin served to inhibit the adherence of intact cells to the surface of the mineral, indicating that the protein and the cells adhered to the pyrite in a mutually exclusive manner. Taken together, these observations support a model where aporusticyanin located on the surface of the bacterial cell acts as a mineral-specific receptor for the initial adherence of At. ferrooxidans to solid pyrite; 6. The specific adhesion of L. ferriphilum to pyrite was mediated by a different acid-stable extracellular protein than aporusticyanin; and 7. A prototype integrating cavity absorption meter (ICAM) was assembled to determine whether this novel spectrophotometer could be used to study cellular respiration in situ.

  15. Title 11 Alaska Administrative Code 82 Mineral Leasing Procedures...

    Open Energy Info (EERE)

    2 Mineral Leasing Procedures Jump to: navigation, search OpenEI Reference LibraryAdd to library Legal Document- RegulationRegulation: Title 11 Alaska Administrative Code 82 Mineral...

  16. Indian Mineral Development Act of 1982 | Open Energy Information

    Open Energy Info (EERE)

    agreements with DOI approval References Indian Mineral Development Act of 19821 Bureau of Indian Affairs2 The Indian Mineral Development Act of 1982 (IMDA) 25 U.S.C. Secs....

  17. Title 36 CFR 228 Minerals | Open Energy Information

    Open Energy Info (EERE)

    Regulation: Title 36 CFR 228 MineralsLegal Abstract Part 228 Minerals under Title 36: Parks, Forests, and Public Property of the U.S. Code of Federal Regulations, current as of...

  18. File:03AKDStateNoncompetitiveMineralLeasingProcess.pdf | Open...

    Open Energy Info (EERE)

    3AKDStateNoncompetitiveMineralLeasingProcess.pdf Jump to: navigation, search File File history File usage Metadata File:03AKDStateNoncompetitiveMineralLeasingProcess.pdf Size of...

  19. A Comparative Study of the Water Gas Shift Reaction Over Platinum Catalysts Supported on CeO2, TiO2 and Ce-Modified TiO2

    SciTech Connect (OSTI)

    Gonzalez, I.; Navarro, R; Wen, W; Marinkovic, N; Rodriguez, J; Rosa, F; Fierro, J

    2010-01-01

    WGS reaction has been investigated on catalysts based on platinum supported over CeO{sub 2}, TiO{sub 2} and Ce-modified TiO{sub 2}. XPS and XANES analyses performed on calcined catalysts revealed a close contact between Pt precursors and cerium species on CeO{sub 2} and Ce-modified TiO{sub 2} supports. TPR results corroborate the intimate contact between Pt and cerium entities in the Pt/Ce-TiO{sub 2} catalyst that facilitates the reducibility of the support at low temperatures while the Ce-O-Ti surface interactions established in the Ce-modified TiO{sub 2} support decreases the reduction of TiO{sub 2} at high temperature. The changes in the support reducibility leads to significant differences in the WGS activity of the studied catalysts. Pt supported on Ce-modified TiO{sub 2} support exhibits better activity than those corresponding to individual CeO{sub 2} and TiO{sub 2}-supported catalysts. Additionally, the Ce-TiO{sub 2}-supported catalyst displays better stability at reaction temperatures higher than 573 K that observed on pure TiO{sub 2}-supported counterpart. Activity measurements, when coupled with the physicochemical characterization of catalysts suggest that the modifications in the surface reducibility of the support play an essential role in the enhancement of activity and stability observed when Pt is supported on the Ce-modified TiO{sub 2} substrate.

  20. H. R. S. 182 - Reservation and Disposition of Government Mineral...

    Open Energy Info (EERE)

    (Redirected from Hawaii Revised Statute 182-1, Definitions for Reservation and Disposition of Government Mineral Rights)...

  1. Diagenesis and clay mineral formation at Gale Crater, Mars (Journal

    Office of Scientific and Technical Information (OSTI)

    Article) | SciTech Connect Journal Article: Diagenesis and clay mineral formation at Gale Crater, Mars Citation Details In-Document Search Title: Diagenesis and clay mineral formation at Gale Crater, Mars The Mars Science Laboratory rover Curiosity found host rocks of basaltic composition and alteration assemblages containing clay minerals at Yellowknife Bay, Gale Crater. On the basis of the observed host rock and alteration minerals, we present results of equilibrium thermochemical modeling

  2. IEED Energy and Mineral Development Grants

    Broader source: Energy.gov [DOE]

    The Secretary of the Interior, through the Office of lndian Energy and Economic Development (IEED), is soliciting grant proposals from federally recognized Indian tribes and tribal energy resource development organizations for projects that assess, evaluate, or otherwise promote the processing, use, or development of energy and mineral resources on Indian lands. Grant awards are subject to the availability of funds as appropriated by Congress and allotted to IEED.

  3. NM Energy Minerals & Natural Resources Department

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Energy Minerals & Natural Resources Department - Sandia Energy Energy Search Icon Sandia Home Locations Contact Us Employee Locator Energy & Climate Secure & Sustainable Energy Future Stationary Power Energy Conversion Efficiency Solar Energy Wind Energy Water Power Supercritical CO2 Geothermal Natural Gas Safety, Security & Resilience of the Energy Infrastructure Energy Storage Nuclear Power & Engineering Grid Modernization Battery Testing Nuclear Fuel Cycle Defense Waste

  4. LOW TEMPERATURE GEOTHERMAL MINERAL RECOVERY PROGRAM

    Broader source: Energy.gov [DOE]

    This targeted initiative focuses on critical mineral extraction as a path to optimize the value stream of low-to-moderate temperature resources. The FOA aims to promote the advancement of thermal energy processes capable of converting geothermal heat sources into power, in conjunction with the development or exploitation of technologies capable of capturing, concentrating, and/or purifying valuable materials contained within geothermal brines to economically extract resources that can provide additional revenue streams to geothermal operators.

  5. Thermodynamic and Transport Properties of YTe3, LaTe3 and CeTe3

    SciTech Connect (OSTI)

    Ru, N.

    2011-08-19

    Measurements of heat capacity, susceptibility, and electrical resistivity are presented for single crystals of the charge density wave compounds YTe{sub 3}, LaTe{sub 3}, and CeTe{sub 3}. The materials are metallic to low temperatures, but have a small density of states due to the charge density wave gapping large portions of the Fermi surface. CeTe{sub 3} is found to be a weak Kondo lattice, with an antiferromagnetic ground state and T{sub N} = 2.8 K. The electrical resistivity of all three compounds is highly anisotropic, confirming the weak dispersion perpendicular to Te planes predicted by band structure calculations.

  6. Optical properties of the Ce and La ditelluride charge density wave compounds

    SciTech Connect (OSTI)

    Lavagnini, M.; Sacchetti, A.; Degiorgi, L.; Shin, K.Y.; Fisher, I.R.; /Stanford U., Geballe Lab. /Stanford U., Appl. Phys. Dept.

    2010-02-15

    The La and Ce di-tellurides LaTe{sub 2} and CeTe{sub 2} are deep in the charge-density-wave (CDW) ground state even at 300 K. We have collected their electrodynamic response over a broad spectral range from the far infrared up to the ultraviolet. We establish the energy scale of the single particle excitation across the CDW gap. Moreover, we find that the CDW collective state gaps a very large portion of the Fermi surface. Similarly to the related rare earth tri-tellurides, we envisage that interactions and Umklapp processes play a role in the onset of the CDW broken symmetry ground state.

  7. Ferromagnetic Kondo lattice CeRuSi{sub 2} with non-Fermi-liquid behavior

    SciTech Connect (OSTI)

    Nikiforov, V. N.; Baran, M.; Irkhin, V. Yu.

    2013-05-15

    The structure, electronic, thermodynamic, and magnetic properties of the CeRuSi{sub 2} Kondo lattice with ferromagnetic ordering characterized by a small moment of the ground state are investigated. Anomalies in the temperature dependences of heat capacity and resistivity (unusual power or logarithmic behavior) observed in the low-temperature range indicate a non-Fermi-liquid behavior. The results are compared with those for other Ce{sub l}Ru{sub n}X{sub m} compounds and anomalous systems based on rare-earth elements and actinides that had been studied earlier.

  8. {ital Ab Initio} Calculation of Crystalline Electric Fields and Kondo Temperatures in Ce Compounds

    SciTech Connect (OSTI)

    Han, J.; Alouani, M.; Cox, D.; Han, J.; Cox, D.; Alouani, M.

    1997-02-01

    We have calculated the band-f hybridizations for Ce{sub x}La{sub 1-x}M{sub 3} compounds (x=1 and x{r_arrow}0; M=Pb,In,Sn,Pd) within the local density approximation and fed this into a noncrossing approximation for the Anderson impurity model applied to both dilute and concentrated limits. Our calculations produce crystalline electric field splittings and Kondo temperatures with trends in good agreement with experiment and demonstrate the need for detailed electronic structure information on hybridization to describe the diverse behaviors of these Ce compounds. {copyright} {ital 1997} {ital The American Physical Society}

  9. (U) Analysis of shock-initiated PBX-9501 through porous CeO2

    SciTech Connect (OSTI)

    Fredenburg, David A.; Dattelbaum, Dana Mcgraw; Dennis-Koller, Darcie

    2015-07-24

    The attenuation properties of an impact initiated PBX-9501 explosive through several thicknesses of CeO2 powder is investigated. The CeO2 is at an initial porous density of 4.0 g/cm3 , roughly 55 % of theoretical maximum density. Measurements of the input (into the powder) and propagated (through the powder) wave profiles are measured using optical velocimetry. Results show a reduction of the average wave speed, CX, and peak steady-state material velocity, uP , with increasing powder thickness from 1.5 - 5.0 mm.

  10. Mechanism of Methane Chemical Looping Combustion with Hematite Promoted with CeO2

    SciTech Connect (OSTI)

    Miller, Duane D.; Siriwardane, Ranjani

    2013-08-01

    Chemical looping combustion (CLC) is a promising technology for fossil fuel combustion that produces sequestration-ready CO{sub 2} stream, reducing the energy penalty of CO{sub 2} separation from flue gases. An effective oxygen carrier for CLC will readily react with the fuel gas and will be reoxidized upon contact with oxygen. This study investigated the development of a CeO{sub 2}-promoted Fe{sub 2}O{sub 3}?hematite oxygen carrier suitable for the methane CLC process. Composition of CeO{sub 2} is between 5 and 25 wt % and is lower than what is generally used for supports in Fe{sub 2}O{sub 3} carrier preparations. The incorporation of CeO{sub 2} to the natural ore hematite strongly modifies the reduction behavior in comparison to that of CeO{sub 2} and hematite alone. Temperature-programmed reaction studies revealed that the addition of even 5 wt % CeO{sub 2} enhances the reaction capacity of the Fe{sub 2}O{sub 3} oxygen carrier by promoting the decomposition and partial oxidation of methane. Fixed-bed reactor data showed that the 5 wt % cerium oxides with 95 wt % iron oxide produce 2 times as much carbon dioxide in comparison to the sum of carbon dioxide produced when the oxides were tested separately. This effect is likely due to the reaction of CeO{sub 2} with methane forming intermediates, which are reactive for extracting oxygen from Fe{sub 2}O{sub 3} at a considerably faster rate than the rate of the direct reaction of Fe{sub 2}O{sub 3} with methane. These studies reveal that 5 wt % CeO{sub 2}/Fe{sub 2}O{sub 3} gives stable conversions over 15 reduction/oxidation cycles. Lab-scale reactor studies (pulsed mode) suggest the methane reacts initially with CeO{sub 2} lattice oxygen to form partial oxidation products (CO + H{sub 2}), which continue to react with oxygen from neighboring Fe{sub 2}O{sub 3}, leading to its complete oxidation to form CO{sub 2}. The reduced cerium oxide promotes the methane decomposition reaction to form C + H{sub 2}, which continue to react with Fe{sub 2}O{sub 3}/Fe{sub 3}O{sub 4} to form CO/CO{sub 2} and H{sub 2}O. This mechanism is supported by the characterization studies, which also suggest that the formation of carbonaceous intermediates may affect the reaction rate and selectivity of the oxygen carrier.

  11. Momentum-space structure of quasielastic spin fluctuations in Ce 3 Pd 20 Si

    Office of Scientific and Technical Information (OSTI)

    6 (Journal Article) | SciTech Connect Momentum-space structure of quasielastic spin fluctuations in Ce 3 Pd 20 Si 6 Citation Details In-Document Search Title: Momentum-space structure of quasielastic spin fluctuations in Ce 3 Pd 20 Si 6 Authors: Portnichenko, P. Y. ; Cameron, A. S. ; Surmach, M. A. ; Deen, P. P. ; Paschen, S. ; Prokofiev, A. ; Mignot, J.-M. ; Strydom, A. M. ; Telling, M. T. F. ; Podlesnyak, A. ; Inosov, D. S. Publication Date: 2015-03-13 OSTI Identifier: 1179978 Type:

  12. Pressure-Induced Structural Phase Transition in CeNi: X-ray and Neutron

    Office of Scientific and Technical Information (OSTI)

    Scattering Studies and First-Principles Calculations (Journal Article) | SciTech Connect Pressure-Induced Structural Phase Transition in CeNi: X-ray and Neutron Scattering Studies and First-Principles Calculations Citation Details In-Document Search Title: Pressure-Induced Structural Phase Transition in CeNi: X-ray and Neutron Scattering Studies and First-Principles Calculations Authors: Mirmelstein, A ; Podlesnyak, A ; dos Santos, A M ; Ehlers, G ; Kerbel, O ; Matvienko, V ; Sefat, A S ;

  13. Neutron Scattering of CeNi at the SNS-ORNL: A Preliminary Report

    Office of Scientific and Technical Information (OSTI)

    (Conference) | SciTech Connect Conference: Neutron Scattering of CeNi at the SNS-ORNL: A Preliminary Report Citation Details In-Document Search Title: Neutron Scattering of CeNi at the SNS-ORNL: A Preliminary Report × You are accessing a document from the Department of Energy's (DOE) SciTech Connect. This site is a product of DOE's Office of Scientific and Technical Information (OSTI) and is provided as a public service. Visit OSTI to utilize additional information resources in energy

  14. Magnetic properties of Ce{sup 3+} in Pb{sub 1{minus}x}Ce{sub x}Se: Kondo and crystal-field effect

    SciTech Connect (OSTI)

    Gratens, X.; Charar, S.; Averous, M.; Isber, S.; Deportes, J.; Golacki, Z.

    1997-10-01

    Electron paramagnetic resonance (EPR) experiments were performed on a Pb{sub 1{minus}x}Ce{sub x}Se crystal at liquid-helium temperatures and show very clearly that the doublet {Gamma}{sub 7} is the ground state for cerium ions. The cubic symmetry is shown and the effective Land{acute e} factor for the Ce{sup 3+} is determined to be 1.354{plus_minus}0.003. An orbital reduction factor is introduced to explain the g experimental value. High-field magnetization results are in good agreement with the EPR results. The nominal Ce composition in PbSe deduced from saturation of the magnetization, x=0.0405{plus_minus}0.0003, is very closed to the value determined by microprobe analysis (x=0.04). At 1.5 K, an antiferromagnetic interaction between the nearest-neighbor cerium atoms is found, J{sub ex}/k{sub B}={minus}0.715thinspK. The low-field magnetic-susceptibility results show that the magnetic moment of cerium impurities is strongly temperature dependent, explained by the presence of the crystal-field effect and the Kondo effect. {copyright} {ital 1997} {ital The American Physical Society}

  15. The synthesis and optical property of solid-state-prepared YAG:Ce phosphor by a spray-drying method

    SciTech Connect (OSTI)

    Lee, H.-M.; Cheng, C.-C.; Huang, C.-Y.

    2009-05-06

    Ce{sup 3+}-activated yttrium aluminum garnet (Y{sub 3}Al{sub 5}O{sub 12}:Ce, YAG:Ce) powder as luminescent phosphor was synthesized by the solid-state reaction method. The phase identification, microstructure and photoluminescent properties of the products were investigated by X-ray powder diffraction (XRD), scanning electron microscopy (SEM), absorption spectrum and photoluminescence (PL) analysis. Spherical phosphor particle is considered better than irregular-shaped particle to improve PL property and application, so this phosphor was granulated into a sphere-like shape by a spray-drying device. After calcinating at 1500 deg. C for 0, 4, and 8 h, the product was identified as YAG and CeO{sub 2} phases. The CeO{sub 2} phase content is decreased by increasing the calcination time or decreasing the Ce{sup 3+} doping content. The product showed higher emission intensity resulted from more Ce{sup 3+} content and larger grain size. The product with CeO{sub 2} was found to have lower emission intensity. This paper presents the crystal structures of Rietveld refinement results of powder XRD data.

  16. Phase transition and possible metallization in CeVO{sub 4} under pressure

    SciTech Connect (OSTI)

    Garg, Alka B.; Shanavas, K.V.; Wani, B.N.; Sharma, Surinder M.

    2013-07-15

    Phase stability of CeVO{sub 4} under pressure has been investigated using synchrotron based angle dispersive x-ray diffraction (ADXRD), electrical resistance and first principles calculations. The results indicate that the ambient zircon structure of the compound transforms to a low symmetry monoclinic monazite phase beyond 3.8 GPa with nearly 8.6% volume discontinuity. Beyond 11 GPa, the pattern could be fitted to a similar monazite structure which is about 12.7% denser and has a much larger monoclinic beta angle. On pressure release the first monoclinic phase is recovered. The electrical resistance data show a large drop in resistance with pressure indicating substantial narrowing down of the band gap. Electronic structure calculations support these observations and suggest possible pressure induced metallization in this material. - Pressure induced structural phase transition in CeVO{sub 4} as observed by x- ray diffraction (pressure vs. volume) and possible metallization in CeVO{sub 4} through electrical resistance and first principles electronic structure calculations. - Highlights: Structural and electrical behavior of CeVO{sub 4} under pressure studied using x-ray diffraction and electrical resistance measurements and first principles calculations. Two successive structural transitions confirmed by experiment and theory: zirconmonazite Imonazite II. Band gap collapse and possible metallization is indicated by electrical resistance measurements and electronic structure calculations under pressure. Novel observation of lower bulk modulus in the high pressure phase (both by experiment and calculations) explained through structural analysis.

  17. Influence of Electron Doping on Magnetic Order in CeRu2Al10

    SciTech Connect (OSTI)

    Kobayashi, Riki; Kaneko, Koji; Saito, Kotaro; Mignot, Jean-Michel; Andre, Gilles; Robert, Julien; Wakimoto, Shuichi; Matsuda, Masaaki; Chi, Songxue; Haga, Yoshinori; Matsuda, Tatsuma; Yamamoto, Etsuji; Nishioka, Takashi; Tanida, Hiroshi; Sera, Masafumi

    2014-01-01

    The effect of electron doping by the substitution of Rh for Ru on unconventional magnetic order in CeRu2Al10 was investigated via neutron powder diffraction. In Ce(Ru1 xRhx)2Al10 with x = 0.05, 0.12, and 0.2, reorientation of the ordered moment from the c-axis as in pure CeRu2Al10 to the a-axis takes place in all samples, while the ordering vector q 0; 1; 0 remains unchanged within this concentration range. The moment reorientation is accompanied by an increase in its size by a factor of 2.4, from = 0.43 B at x = 0 to = 1.06, 1.04, and 1.02 B for x = 0.05, 0.12, and 0.2, respectively. The continuous decrease in the N el temperature T0(TN), despite an abrupt increase in , underlines the strong anisotropy in the exchange interaction in CeRu2Al10 and the fact that this anisotropy is easily suppressed by electron doping. 1.

  18. Charge dynamics of Ce-based compounds: Connection between the mixed valent and Kondo-insulator states

    SciTech Connect (OSTI)

    Bucher, B. [Laboratorium fuer Festkoerperphysik, Eidgenoessische Technische Hochschule Zuerich, 8093 Zuerich (Switzerland)] [Laboratorium fuer Festkoerperphysik, Eidgenoessische Technische Hochschule Zuerich, 8093 Zuerich (Switzerland); Schlesinger, Z. [IBM, Thomas J. Watson Research Center, Yorktown Heights, New York 10958 (United States)] [IBM, Thomas J. Watson Research Center, Yorktown Heights, New York 10958 (United States); Mandrus, D.; Fisk, Z.; Sarrao, J. [Los Alamos National Laboratory, Los Alamos, New Mexico 87545 (United States)] [Los Alamos National Laboratory, Los Alamos, New Mexico 87545 (United States); DiTusa, J.F.; Oglesby, C.; Aeppli, G.; Bucher, E. [AT& T Bell Laboratories, Murray Hill, New Jersey 07974 (United States)] [AT& T Bell Laboratories, Murray Hill, New Jersey 07974 (United States)

    1996-02-01

    The reflectivities of the mixed-valent compounds CeSn{sub 3} and CePd{sub 3} have been measured to obtain the optical conductivity as a function of temperature. Both compounds show a renormalization of the low-energy Drude conductivity at low temperatures. In addition, for the low-carrier-density compound CePd{sub 3}, but not for high-carrier-density CeSn{sub 3}, substantial spectral weight lost from the conductivity below 1000 cm{sup {minus}1} reappears in the frequency range 2000{endash}10000 cm{sup {minus}1}, indicating that CePd{sub 3} can be considered a lightly doped Kondo insulator. {copyright} {ital 1996 The American Physical Society.}

  19. (U) Equation of State and Compaction Modeling for CeO2

    SciTech Connect (OSTI)

    Fredenburg, David A.; Chisolm, Eric D.

    2014-10-20

    Recent efforts have focused on developing a solid-liquid and three-phase equation of state (EOS) for CeO2, while parallel experimental efforts have focused on obtaining high-fidelity Hugoniot measurements on CeO2 in the porous state. The current work examines the robustness of two CeO2 SESAME equations of state, a solid-liquid EOS, 96170, and a three-phase EOS, 96171, by validating the EOS against a suite of high-pressure shock compression experiments on initially porous CeO2. At lower pressures compaction is considered by incorporating a two-term exponential form of the P-compaction model, using three separate definitions for ?(P). Simulations are executed spanning the partially compacted and fully compacted EOS regimes over the pressure range 0.5 - 109 GPa. Comparison of calculated Hugoniot results with those obtained experimentally indicate good agreement for all definitions of ?(P) with both the solid-liquid and three-phase EOS in the low-pressure compaction regime. At higher pressures the three-phase EOS does a better job at predicting the measured Hugoniot response, though at the highest pressures EOS 96171 predicts a less compliant response than is observed experimentally. Measured material velocity profiles of the shock-wave after it has transmitted through the powder are also compared with those simulated using with solid-liquid and three-phase EOS. Profiles lend insight into limits of the current experimental design, as well as the threshold conditions for the shock-induced phase transition in CeO2.

  20. Synthesis and crystal structure of two new cerium rhodium oxides: Ce{sub 2/3-x}Rh{sup 3+}{sub 2}O{sub 4} (x{approx}0.12) with Ce mixed valency and Ce{sup 4+}Rh{sup 3+}{sub 2}O{sub 5}

    SciTech Connect (OSTI)

    Mizoguchi, Hiroshi; Zakharov, L.N.; Bhuvanesh, N.S.P.; Sleight, A.W.; Subramanian, M.A.

    2011-06-15

    The new compounds Ce{sub 2/3-x}Rh{sub 2}O{sub 4} (x{approx}0.11-0.14) and CeRh{sub 2}O{sub 5} have been prepared. Their structures were determined from single crystal X-ray diffraction data. Electrical and magnetic properties were also evaluated. Based on the structural analysis and physical properties, oxidation states for CeRh{sub 2}O{sub 5} can be assigned as Ce{sup 4+}Rh{sup 3+}{sub 2}O{sub 5}. A small variation in x was detected for Ce{sub 2/3-x}Rh{sub 2}O{sub 4} indicating a formula ranging from Ce{sup 3.64+}{sub 0.55}Rh{sup 3+}{sub 2}O{sub 4} to Ce{sup 3.81+}{sub 0.525}Rh{sup 3+}{sub 2}O{sub 4}. - Graphical abstract: The new compounds Ce{sub 2/3-x}Rh{sub 2}O{sub 4} (x{approx}0.11-0.14) and CeRh{sub 2}O{sub 5} have been prepared and their structures were determined from single crystal X-ray diffraction data. Electrical and magnetic properties were also evaluated. Highlights: > The new compounds CeRh{sub 2}O{sub 5} and Ce{sub 2/3-x}Rh{sub 2}O{sub 4} (x{approx}0.11-0.14) have been prepared. > Their structures were determined from single crystal X-ray diffraction data. > Valence picture is Ce{sup 4+}Rh{sup 3+}{sub 2}O{sub 5} and Ce{sup 3.64+}{sub 0.55}Rh{sup 3+}{sub 2}O{sub 4} to Ce{sup 3.81+}{sub 0.525}Rh{sup 3+}{sub 2}O{sub 4}.

  1. SkyMine Carbon Mineralization Pilot Project

    SciTech Connect (OSTI)

    Christenson, Norm; Walters, Jerel

    2014-12-31

    This Topical Report addresses accomplishments achieved during Phase 2b of the SkyMine® Carbon Mineralization Pilot Project. The primary objectives of this project are to design, construct, and operate a system to capture CO2 from a slipstream of flue gas from a commercial coal-fired cement kiln, convert that CO2 to products having commercial value (i.e., beneficial use), show the economic viability of the CO2 capture and conversion process, and thereby advance the technology to the point of readiness for commercial scale demonstration and deployment. The overall process is carbon negative, resulting in mineralization of CO2 that would otherwise be released into the atmosphere. The project will also substantiate market opportunities for the technology by sales of chemicals into existing markets, and identify opportunities to improve technology performance and reduce costs at the commercial scale. The project is being conducted in two phases. The primary objectives of Phase 1 were to evaluate proven SkyMine® process chemistry for commercial pilot-scale operation and complete the preliminary design for the pilot plant to be built and operated in Phase 2, complete a NEPA evaluation, and develop a comprehensive carbon life cycle analysis. The objective of Phase 2b was to build the pilot plant to be operated and tested in Phase 2c.

  2. Structure and magnetic properties of Ce?(Ni/Al/Ga)??A new phase with the La?Al?? structure type

    SciTech Connect (OSTI)

    Janka, Oliver; Shang, Tian; Baumbach, Ryan E.; Bauer, Eric D.; Thompson, Joe D.; Kauzlarich, Susan M.

    2015-03-01

    Single crystals of Ce?(Ni/Al/Ga)?? were obtained from an Al flux reaction. Single crystals of the title compound crystallizing in the orthorhombic space group Immm (No. 71, Z = 2) with a = 436.38(14), b = 1004.5(3) and c = 1293.4(4) pm. This is a standardized unit cell of the previously published La?Al?? structure type. Wavelength dispersive microprobe provides the composition of Ce?.?????Ni?.?????Al?.?????Ga?.?????. Single crystal refinement provides the composition Ce?Ni?.??Al?.??Ga?.?? with substitution of the Ni and Ga on the Al1 and Al4 sites with the Al2 and Al3 solely occupied by Al. Magnetic susceptibility measurements reveal antiferromagnetic ordering with TN = 4.8 K and there is no evidence for a ferromagnetic ordering that has been reported for Ce?Al??. The effective magnetic moment was found to be ?eff = 1.9?B/Ce, which is lower than the expected value for trivalent Ce (2.54?B/Ce).

  3. Selective flotation of phosphate minerals with hydroxamate collectors

    DOE Patents [OSTI]

    Miller, Jan D.; Wang, Xuming; Li, Minhua

    2002-01-01

    A method is disclosed for separating phosphate minerals from a mineral mixture, particularly from high-dolomite containing phosphate ores. The method involves conditioning the mineral mixture by contacting in an aqueous in environment with a collector in an amount sufficient for promoting flotation of phosphate minerals. The collector is a hydroxamate compound of the formula; ##STR1## wherein R is generally hydrophobic and chosen such that the collector has solubility or dispersion properties it can be distributed in the mineral mixture, typically an alkyl, aryl, or alkylaryl group having 6 to 18 carbon atoms. M is a cation, typically hydrogen, an alkali metal or an alkaline earth metal. Preferably, the collector also comprises an alcohol of the formula, R'--OH wherein R' is generally hydrophobic and chosen such that the collector has solubility or dispersion properties so that it can be distributed in the mineral mixture, typically an alkyl, aryl, or alkylaryl group having 6 to 18 carbon atoms.

  4. CMI Course Inventory: Mineral Economics and Business | Critical Materials

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Institute Mineral Economics and Business Mineral Economics and Business Of the six CMI Team members that are educational institutions, two offer courses in Mineral Economics and Business. These are Colorado School of Mines and Brown University. The following links go to the class list on the CMI page for that school. Colorado School of Mines offers a major in these areas At Brown University, the Institute of Environment and Society offers several courses on economics and policy CMI Education

  5. Before the House Natural Resources Subcommittee on Energy and Mineral

    Energy Savers [EERE]

    Resources | Department of Energy Natural Resources Subcommittee on Energy and Mineral Resources Before the House Natural Resources Subcommittee on Energy and Mineral Resources Before the House Natural Resources Subcommittee on Energy and Mineral Resources By: Dr. Ray Boswell, Senior Management and Technology Advisor, National Energy Technology Laboratory Subject: Unconventional Fuels, Part II: The Promise of Methane Hydrates PDF icon 7-30-09_Final_Testimony_(Boswell).pdf More Documents &

  6. Magnitude of the magnetic exchange interaction in the heavy-fermion antiferromagnet CeRhIn5

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Das, Pinaki; Lin, S. -Z.; Ghimire, N. J.; Huang, K.; Ronning, F.; Bauer, E. D.; Thompson, J. D.; Batista, C. D.; Ehlers, G.; Janoschek, M.

    2014-12-08

    We have used high-resolution neutron spectroscopy experiments to determine the complete spin wave spectrum of the heavy-fermion antiferromagnet CeRhIn₅. The spin wave dispersion can be quantitatively reproduced with a simple frustrated J₁-J₂ model that also naturally explains the magnetic spin-spiral ground state of CeRhIn₅ and yields a dominant in-plane nearest-neighbor magnetic exchange constant J₀=0.74(3) meV. Our results lead the way to a quantitative understanding of the rich low-temperature phase diagram of the prominent CeTIn₅ (T = Co, Rh, Ir) class of heavy-fermion materials.

  7. Magnitude of the magnetic exchange interaction in the heavy-fermion antiferromagnet CeRhIn5

    SciTech Connect (OSTI)

    Das, Pinaki; Lin, S. -Z.; Ghimire, N. J.; Huang, K.; Ronning, F.; Bauer, E. D.; Thompson, J. D.; Batista, C. D.; Ehlers, G.; Janoschek, M.

    2014-12-08

    We have used high-resolution neutron spectroscopy experiments to determine the complete spin wave spectrum of the heavy-fermion antiferromagnet CeRhIn?. The spin wave dispersion can be quantitatively reproduced with a simple frustrated J?-J? model that also naturally explains the magnetic spin-spiral ground state of CeRhIn? and yields a dominant in-plane nearest-neighbor magnetic exchange constant J?=0.74(3) meV. Our results lead the way to a quantitative understanding of the rich low-temperature phase diagram of the prominent CeTIn? (T = Co, Rh, Ir) class of heavy-fermion materials.

  8. Division of Energy and Mineral Development | Open Energy Information

    Open Energy Info (EERE)

    in Lakewood, Colorado. The Division assists Tribes with the exploration, development and management of their energy and mineral resources to create sustainable economies for...

  9. National Mineral Development Corporation Ltd NMDC | Open Energy...

    Open Energy Info (EERE)

    Corporation Ltd NMDC Jump to: navigation, search Name: National Mineral Development Corporation Ltd. (NMDC) Place: Hyderabad, Andhra Pradesh, India Zip: 500028 Sector: Solar, Wind...

  10. Clay Minerals Related To The Hydrothermal Activity Of The Bouillante...

    Open Energy Info (EERE)

    Minerals Related To The Hydrothermal Activity Of The Bouillante Geothermal Field (Guadeloupe) Jump to: navigation, search OpenEI Reference LibraryAdd to library Journal Article:...

  11. Molecular Simulation of Carbon Dioxide Brine and Clay Mineral...

    Office of Scientific and Technical Information (OSTI)

    Title: Molecular Simulation of Carbon Dioxide Brine and Clay Mineral Interactions and Determination of Contact Angles. Abstract not provided. Authors: Tenney, Craig M ; Cygan, ...

  12. Oxygen And Carbon Isotope Ratios Of Hydrothermal Minerals From...

    Open Energy Info (EERE)

    Oxygen And Carbon Isotope Ratios Of Hydrothermal Minerals From Yellowstone Drill Cores Jump to: navigation, search OpenEI Reference LibraryAdd to library Journal Article: Oxygen...

  13. Buckhorn Mineral Wells Space Heating Low Temperature Geothermal...

    Open Energy Info (EERE)

    Space Heating Low Temperature Geothermal Facility Jump to: navigation, search Name Buckhorn Mineral Wells Space Heating Low Temperature Geothermal Facility Facility Buckhorn...

  14. Thermally Speciated Mercury in Mineral Exploration | Open Energy...

    Open Energy Info (EERE)

    Speciated Mercury in Mineral Exploration Abstract Abstract unavailable. Author S.C. Smith Conference IGES; Dublin, CA; 20030901 Published IGES, 2003 DOI Not Provided Check...

  15. Mineral Leasing Act of 1920 | Open Energy Information

    Open Energy Info (EERE)

    Leasing Act established the authority of the Secretary of the Interior to oversee oil and gas operations on federal land. References Federal Oil and Gas Statutes1 Mineral...

  16. Mining and Minerals Policy Act of 1970 | Open Energy Information

    Open Energy Info (EERE)

    Act, this statute encompasses both hard rock mining and oil and gas and established modern federal policy regarding mineral resources in the United States. The Act articulates a...

  17. Radioactive Mineral Occurences in Nevada | Open Energy Information

    Open Energy Info (EERE)

    Radioactive Mineral Occurences in Nevada Abstract Abstract unavailable. Author Larry J. Garside Organization Nevada Bureau of Mines and Geology Published Nevada Bureau of...

  18. Hawaii Revised Statute 523A-2, Definition of Mineral Resources...

    Open Energy Info (EERE)

    Not provided DOI Not Provided Check for DOI availability: http:crossref.org Online Internet link for Hawaii Revised Statute 523A-2, Definition of Mineral Resources Citation...

  19. DOE - Office of Legacy Management -- International Minerals and...

    Office of Legacy Management (LM)

    (The Former International Minerals and Chemical Corporation) Bartow, Florida; November 26, 1985 FL.03-4 - Memorandum; McKereghan to Campbell; ERDA (AEC) Inspection; April 11, 1977...

  20. Astoria Mineral Hot Springs Pool & Spa Low Temperature Geothermal...

    Open Energy Info (EERE)

    Astoria Mineral Hot Springs Sector Geothermal energy Type Pool and Spa Location Jackson, Wyoming Coordinates 43.4799291, -110.7624282 Show Map Loading map......

  1. Mineral County, West Virginia: Energy Resources | Open Energy...

    Open Energy Info (EERE)

    West Virginia Keyser, West Virginia Piedmont, West Virginia Ridgeley, West Virginia Wiley Ford, West Virginia Retrieved from "http:en.openei.orgwindex.php?titleMineralCou...

  2. Request for Information explores mineral recovery from geothermal...

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Information explores mineral recovery from geothermal fluids May 12, 2015 - 11:01am Addthis Geothermal energy below the boiling point is now being harnessed to generate electricity ...

  3. Cooperative Reorganization of Mineral and Template during Directed...

    Office of Scientific and Technical Information (OSTI)

    prepared from organic thiol molecules on metal substrates are known to exert substantial influence over mineralization and, as such, provide model systems for investigating the...

  4. Australasian Code for Reporting of Exploration Results, Mineral...

    Open Energy Info (EERE)

    (JORC) Published The Joint Ore Reserves Committee of The Australasian Institute of Mining and Metallurgy, Australian Institute of Geoscientists, and Minerals Council of...

  5. Hyperspectral Mineral Mapping In Support Of Geothermal Exploration...

    Open Energy Info (EERE)

    CA and Dixie Valley, NV, USA Jump to: navigation, search OpenEI Reference LibraryAdd to library Conference Paper: Hyperspectral Mineral Mapping In Support Of Geothermal...

  6. Discovery of bridgmanite, the most abundant mineral in Earth...

    Office of Scientific and Technical Information (OSTI)

    SciTech Connect Search Results Journal Article: Discovery of bridgmanite, the most abundant mineral in Earth, in a shocked meteorite Citation Details In-Document Search Title: ...

  7. Stewart Mineral Springs Pool & Spa Low Temperature Geothermal...

    Open Energy Info (EERE)

    Pool & Spa Low Temperature Geothermal Facility Jump to: navigation, search Name Stewart Mineral Springs Pool & Spa Low Temperature Geothermal Facility Facility Stewart...

  8. Respiratory disease in Utah coal miners

    SciTech Connect (OSTI)

    Rom, W.N.; Kanner, R.E.; Renzetti, A.D. Jr.; Shigeoka, J.W.; Barkman, H.W.; Nichols, M.; Turner, W.A.; Coleman, M.; Wright, W.E.

    1981-04-01

    Two hundred forty-two Utah underground coal miners volunteered to participate in a respiratory disease study. They were an older group (mean, 56 years of age) and had spent a mean of 29 years in the coal-mining industry. The prevalence of chronic bronchitis was 57%, and that of coal worker's pneumoconiosis, 25%; only one worker had progressive massive fibrosis. Significant impairment of pulmonary function was found among those with a history of cigarette smoking. Chronic bronchitis or coal worker's penumoconiosis among nonsmokers did not impair pulmonary function. There was a significant association among the nonsmokers between increasing exposure to coal dust and coal worker's pneumoconiosis, but not for changes in pulmonary function. Coal mine dust had a significant influence in causing the symptom complex of chronic cough and sputum production, and coal worker's pneumoconiosis.

  9. Respiratory disease in Utah coal miners

    SciTech Connect (OSTI)

    Rom, W.N.; Kanner, R.E.; Renzetti, A.D. Jr.; Shigeoka, J.W.; Barkman, H.W.; Nichols, M.; Turner, W.A.; Coleman, M.; Wright, W.E.

    1981-04-01

    Two hundred forty-two Utah underground coal miners volunteered to participate in a respiratory disease study. They were an older group (mean, 56 years of age) and had spent a mean of 29 years in the coal-mining industry. The prevalence of chronic bronchitis was 57%, and that of coal worker's pneumoconiosis, 25%; only one worker had progressive massive fibrosis. Significant impairment of pulmonary function was found among those with a history of cigarette smoking. Chronic bronchitis or coal worker's pneumoconiosis among nonsmokers did not impair pulmonary function. There was a significant association among the nonsmokers between increasing exposure to coal dust and coal worker's pneumoconiosis, but not for changes in pulmonary function. Coal mine dust had a significant influence in causing the symptom complex of chronic cough and sputum production, and coal worker's pneumoconiosis.

  10. Momentum-resolved photoemission of the Kondo peak in an ordered Ce-containing alloy

    SciTech Connect (OSTI)

    Garnier, M.; Purdie, D.; Breuer, K.; Hengsberger, M.; Baer, Y.

    1997-11-01

    A comparison of uv-photoemission spectra recorded from the surface alloys Pt(111)({radical}(3){times}{radical}(3))R30{degree}Ce and Pt(111)(2{times}2)La allows the contribution from the 4f electrons to be seen easily. The valence-band structure of these two surfaces is very similar, and the most obvious 4f contribution in high-resolution photoemission spectra of the Ce-containing alloy is the tail of the Kondo peak cut at E{sub F}. Within the limits of our measurement, no dispersion of this feature in the occupied regime is detected. The Kondo peak displays a marked intensity dependence on the emission angle, suggesting that hybridization is present in only a limited part of reciprocal space. The temperature dependence of this near-E{sub F} feature supports this interpretation. {copyright} {ital 1997} {ital The American Physical Society}

  11. Reactivity and reaction intermediates for acetic acid adsorbed on CeO2(111)

    SciTech Connect (OSTI)

    Calaza, Florencia; Chen, Tsung-Liang; Mullins, David R; Xu, Ye; Overbury, Steven {Steve} H

    2015-01-01

    Adsorption and reaction of acetic acid on a CeO2(1 1 1) surface was studied by a combination of ultra-highvacuum based methods including temperature desorption spectroscopy (TPD), soft X-ray photoelectronspectroscopy (sXPS), near edge X-ray absorption spectroscopy (NEXAFS) and reflection absorption IRspectroscopy (RAIRS), together with density functional theory (DFT) calculations. TPD shows that thedesorption products are strongly dependent upon the initial oxidation state of the CeO2surface, includingselectivity between acetone and acetaldehyde products. The combination of sXPS and NEXAFS demon-strate that acetate forms upon adsorption at low temperature and is stable to above 500 K, above whichpoint ketene, acetone and acetic acid desorb. DFT and RAIRS show that below 500 K, bridge bondedacetate coexists with a moiety formed by adsorption of an acetate at an oxygen vacancy, formed bywater desorption.

  12. Single to Multiquasiparticle Excitations in the Itinerant Helical Magnet CeRhIn5

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Stock, C.; Rodriguez-Rivera, J. A.; Schmalzl, K.; Rodriguez, E. E.; Stunault, A.; Petrovic, C.

    2015-06-19

    Neutron scattering is used to measure the quantum spin fluctuations in CeRhIn5 - the parent material of the eXIn5 superconducting series. Out-of-plane spin fluctuations are gapped and localized in momentum, similar to the spin excitons in CeCoIn5. The in-plane fluctuations consist of sharp spin-wave excitations parameterized by a nearest neighbor exchange JRKKY =0.88 ± 0.05 meV that crossover to a temporally and spatially broad multiparticle spectrum with energies of ~ 2 × JRKKY . This continuum represents composite fluctuations that illustrate the breakdown of single magnons originating from the delicate energy balance between localized 4f and itinerant behavior in amore » heavy metal. The experiment therefore shows how quasiparticle behavior is changed by the close proximity of quantum criticality.« less

  13. Neutron Scattering of CeNi at the Spallation Neutron Source at Oak Ridge

    Office of Scientific and Technical Information (OSTI)

    National Laboratory: A Preliminary Report (Conference) | SciTech Connect Spallation Neutron Source at Oak Ridge National Laboratory: A Preliminary Report Citation Details In-Document Search Title: Neutron Scattering of CeNi at the Spallation Neutron Source at Oak Ridge National Laboratory: A Preliminary Report Authors: Tobin, J G ; Mirmelstein, A V ; Podlesnyak, A ; Kolesnikov, A I Publication Date: 2014-01-16 OSTI Identifier: 1132009 Report Number(s): LLNL-PROC-649216 DOE Contract Number:

  14. Investigation into Nanostructured Lanthanum Halides and CeBr{sub 3} for Nuclear Radiation Detection

    SciTech Connect (OSTI)

    Guss, P., Guise, R., Mukhopadhyay, S., Yuan, D.

    2011-06-22

    This slide-show presents work on radiation detection with nanostructured lanthanum halides and CeBr{sub 3}. The goal is to extend the gamma energy response on both low and high-energy regimes by demonstrating the ability to detect low-energy x-rays and relatively high-energy activation prompt gamma rays simultaneously using the nano-structured lanthanum bromide, lanthanum fluoride, cerium bromide, or other nanocrystal material. Homogeneous and nano structure cases are compared.

  15. Synthesis of Transient Climate Evolution of the last 21-kyr (SynTraCE-21)

    SciTech Connect (OSTI)

    Zhengyu Liu

    2011-05-06

    Climate evolution in the last 21,000 years provides critical observations for testing state-of-the-art climate models on the simulation of climate evolution and abrupt climate changes. Proxy evidences and new modeling activities have led to rapid advances in our understanding of climate change for this past time period. This funding helps to support the first international SynTraCE-21k workshop at Mount Hood, Oregon from 10-13 October, 2010.

  16. DOE 10 CFR Part 429, Docket Number: EERE-2010-BT-CE-0014, RIN

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    1904-AC23, Federal Register Vol. 76, No. 75, 21813-15 (Tuesday, April 19, 2011), Notice of Proposed Rule for Energy Conservation Program: Certification, Compliance, and Enforcement fo | Department of Energy Part 429, Docket Number: EERE-2010-BT-CE-0014, RIN 1904-AC23, Federal Register Vol. 76, No. 75, 21813-15 (Tuesday, April 19, 2011), Notice of Proposed Rule for Energy Conservation Program: Certification, Compliance, and Enforcement fo DOE 10 CFR Part 429, Docket Number:

  17. Remarkably robust and correlated coherence and antiferromagnetism in (Ce1-x Lax)Cu?Ge?

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Hodovanets, H.; Budko, S.? L.; Straszheim, W.? E.; Taufour, V.; Mun, E.? D.; Kim, H.; Flint, R.; Canfield, P.? C.

    2015-06-08

    We present magnetic susceptibility, resistivity, specific heat, and thermoelectric power measurements on (Ce1-x Lax)Cu?Ge? single crystals (0 ? x ? 1). With La substitution, the antiferromagnetic temperature TN is suppressed in an almost linear fashion and moves below 0.36 K, the base temperature of our measurements for x > 0.8. Surprisingly, in addition to robust antiferromagnetism, the system also shows low temperature coherent scattering below Tcoh up to ~ 0.9 of La, indicating a small percolation limit ~ 9% of Ce. Tcoh as a function of magnetic field was found to have different behavior for x more> 0.9. Remarkably, (Tcoh) at H = 0 was found to be linearly proportional to TN. The jump in the magnetic specific heat ?Cm at TN as a function of TK/TN for (Ce1-x Lax)Cu?Ge? follows the theoretical prediction based on the molecular field calculation for the S = 1/2 resonant level model.less

  18. Mineral resources and mineral resource potential of the Panamint Dunes Wilderness Study Area, Inyo County, California

    SciTech Connect (OSTI)

    Kennedy, G.L.; Kilburn, J.E.; Conrad, J.E.; Leszcykowski, A.M.

    1984-01-01

    This report presents the results of a mineral survey of the Panamint Dunes Wilderness Study Area (CDCA-127), California Desert Conservation Area, Inyo County, California. The Panamint Dunes Wilderness Study Area has an identified volcanic cinder resource and few areas with mineral resource potential. Hydrothermal deposits of lead-zinc-silver occur in veins and small replacement bodies along and near the Lemoigne thrust fault on the eastern side of the wilderness study area. Two workings, the Big Four mine with 35,000 tons of inferred subeconomic lead-zinc-silver resources and a moderate potential for additional resources, and the Apple 1 claim with low potential for lead-zinc-silver resources, are surrounded by the study area but are specifically excluded from it. A low resource potential for lead-zinc-silver is assigned to other exposures along the Lemoigne thrust, although metallic minerals were not detected at these places. The Green Quartz prospect, located near the northern tip of the study area, has low resource potential for copper in quartz pegmatities in quartz monzonite of the Hunter Mountain batholith. Nonmetallic mineral resources consist of volcanic cinders and quartz sand. An estimated 900,000 tons of inferred cinder reserves are present at Cal Trans borrow pit MS 242, on the southern margin of the study area. The Panamint Valley dune field, encompassing 480 acres in the north-central part of the study area, has only low resource potential for silica because of impurities. Other sources of silica and outside the study area are of both higher purity and closer to possible markets. 19 refs., 2 figs., 1 tab.

  19. Emission properties and back-bombardment for CeB{sub 6} compared to LaB{sub 6}

    SciTech Connect (OSTI)

    Bakr, Mahmoud; Kawai, M.; Kii, T.; Zen, H.; Masuda, K.; Ohgaki, H.

    2015-02-14

    The emission properties of CeB{sub 6} compared to LaB{sub 6} thermionic cathodes have been measured using an electrostatic DC gun. Obtaining knowledge of the emission properties is the first step in understanding the back-bombardment effect that limits wide usage of thermionic radio-frequency electron guns. The effect of back-bombardment electrons on CeB{sub 6} compared to LaB{sub 6} was studied using a numerical simulation model. The results show that for 6 μs pulse duration with input radio-frequency power of 8 MW, CeB{sub 6} should experience 14% lower temperature increase and 21% lower current density rise compared to LaB{sub 6}. We conclude that CeB{sub 6} has the potential to become the future replacement for LaB{sub 6} thermionic cathodes in radio-frequency electron guns.

  20. Kondo behavior, ferromagnetic correlations, and crystal fields in the heavy Fermion compounds Ce3X (X=In, Sn)

    SciTech Connect (OSTI)

    Wang, C. H.; Lawrence, J. M.; Christianson, Andrew D; Goremychkin, E. A.; Fanelli, V. R.; Gofryk, K.; Bauer, E. D.; Ronning, F.; Thompson, J. D.; De Souza, N. R.; Kolesnikov, Alexander I

    2010-01-01

    We report measuerments of the inelastic neutron scattering, the magnetic susceptibility, the magnetization, and the magnetic field dependence of the specific heat for the heavy Fermion compounds Ce3In and Ce3Sn. The neutron scattering results show that the excited crystal field levels have energies E1=13.2 meV, E2-44.8 meV for Ce3In and E1=18.5 meV, E2=36.1 meV for Ce3Sn. The Kondo temperature deduced from the quasielastic linewidth is 17 K for Ce3In and 40 K for Ce3Sn. The low temperature behavior of teh specific heat, magnetization, and susceptibility can not be well-described by J=1.2 Kondo physics alone, but require calculations that include contributions from the Kondo effect, broadened crystal fields, and ferromagnetic correlations, all of which are known to be important in these compounds. We find that the ferromagnetic fluctuation makes a 10-15% contribution to the ground state entropy and magnetization. The large in this heavy Fermion system thus arises more from the ferromagnetic correlations than from the Kondo behavior.

  1. Effect of oxygen vacancy on half metallicity in Ni-doped CeO{sub 2} diluted magnetic semiconductor

    SciTech Connect (OSTI)

    Saini, Hardev S. Saini, G. S. S.; Singh, Mukhtiyar; Kashyap, Manish K.

    2015-05-15

    The electronic and magnetic properties of Ni-doped CeO{sub 2} diluted amgentic semiconductor (DMS) including the effect of oxygen vacancy (V{sub o}) with doping concentration, x = 0.125 have been calculated using FPLAPW method based on Density Functional Theory (DFT) as implemented in WIEN2k. In the present supercell approach, the XC potential was constructed using GGA+U formalism in which Coulomb correction is applied to standard GGA functional within the parameterization of Perdew-Burke-Ernzerhof (PBE). We have found that the ground state properties of bulk CeO{sub 2} compound have been modified significantly due to the substitution of Ni-dopant at the cation (Ce) site with/without V{sub O} and realized that the ferromagnetism in CeO{sub 2} remarkably depends on the V{sub o} concentrations. The presence of V{sub o}, in Ni-doped CeO{sub 2}, can leads to strong ferromagnetic coupling between the nearest neighboring Ni-ions and induces a HMF in this compound. Such ferromagnetic exchange coupling is mainly attributed to spin splitting of Ni-d states, via electrons trapped in V{sub o}. The HMF characteristics of Ni-doped CeO{sub 2} including V{sub o} makes it an ideal material for spintronic devices.

  2. Soft chemistry synthesis of high-crystalline orthogermanate CeGeO{sub 4}: A new photocatalyst

    SciTech Connect (OSTI)

    Xing Jun; Yang Chen; Li Weikun; Gong Xueqing; Yang Huagui

    2013-01-15

    A new orthogermanate phase of CeGeO{sub 4} was studied and the corresponding nanocrystals have been successfully synthesized via a facile hydrothermal method without adding any capping agent. The pH value of the solution and the reaction time were also further investigated, respectively. The as-prepared CeGeO{sub 4} nanocrystals with a uniform size of 15 nm have been characterized by using XRD/TEM/TGA/UV-vis techniques, and their electronic structures and band gap were calculated based on a plane wave density function theory (DFT). The promising photocatalytic properties of CeGeO{sub 4} have been confirmed through monitoring reactive oxidative species generated in photocatalytic reactions of terephthalic acid as a fluorescence probe. - Graphical Abstract: A novel photocatalyst CeGeO{sub 4} was prepared. Highlights: Black-Right-Pointing-Pointer CeGeO{sub 4} as a novel photocatalyst was successfully synthesized by a hydrothermal method. Black-Right-Pointing-Pointer Electronic structure and band gap were calculated based on DFT. Black-Right-Pointing-Pointer CeGeO{sub 4} exhibited a promising photocatalytic performance.

  3. High thermoelectric performance of In, Yb, Ce multiple filled CoSb{sub 3} based skutterudite compounds

    SciTech Connect (OSTI)

    Ballikaya, Sedat; Department of Physics, University of Michigan, Ann Arbor, MI, 48109 ; Uzar, Neslihan; Yildirim, Saffettin; Salvador, James R.; Uher, Ctirad

    2012-09-15

    Filling voids with rare earth atoms is an effective way to lowering thermal conductivity which necessarily enhances thermoelectric properties of skutterudite compounds. Yb atom is one of the most effective species among the rare earth atoms for filling the voids in the skutterudite structure due to a large atomic mass, radius and it is intermediate valence state. In this work, we aim to find the best filling partners for Yb using different combinations of Ce and In as well as to optimize actual filling fraction in order to achieve high values of ZT. The traditional method of synthesis relying on melting-annealing and followed by spark plasma sintering was used to prepare all samples. The thermoelectric properties of four samples of Yb{sub 0.2}In{sub 0.2}Co{sub 4}Sb{sub 12}, Yb{sub 0.2}Ce{sub 0.15}Co{sub 4}Sb{sub 12}, Yb{sub 0.2}Ce{sub 0.15}In{sub 0.2}Co{sub 4}Sb{sub 12}, and Yb{sub 0.3}Ce{sub 0.15}In{sub 0.2}Co{sub 4}Sb{sub 12} (nominal) were examined based on the Seebeck coefficient, electrical conductivity, thermal conductivity, and Hall coefficient. Hall coefficient and Seebeck coefficient signs confirm that all samples are n-type skutterudite compounds. Carrier density increases with the increasing Yb+Ce content. A high power factor value of 57.7 {mu}W/K{sup 2}/cm for Yb{sub 0.2}Ce{sub 0.15}Co{sub 4}Sb{sub 12} and a lower thermal conductivity value of 2.82 W/m/K for Yb{sub 0.2}Ce{sub 0.15}In{sub 0.2}Co{sub 4}Sb{sub 12} indicate that small quantities of Ce with In may be a good partner to Yb to reduce the thermal conductivity further and thus enhance the thermoelectric performance of skutterudites. The highest ZT value of 1.43 was achieved for Yb{sub 0.2}Ce{sub 0.15}In{sub 0.2}Co{sub 4}Sb{sub 12} triple-filled skutterudite at 800 K. - Graphical abstract: Thermoelectric figure of merit of Yb{sub x}In{sub y}Ce{sub z}Co{sub 4}Sb{sub 12} (0{<=}x,y,z{<=}0.18 actual) compounds versus temperature. Highlights: Black-Right-Pointing-Pointer TE properties of Yb,In,Ce multiple-filled Yb{sub x}In{sub y}Ce{sub z}Co{sub 4}Sb{sub 12} skutterudites were investigated. Black-Right-Pointing-Pointer Thermal conductivity is strongly suppressed by multiple filling of Yb, Ce and In. Black-Right-Pointing-Pointer Small amounts of Ce and In with Yb are beneficial for the enhancement of TE performance. Black-Right-Pointing-Pointer The highest ZT=1.43 was achieved with Yb{sub 0.07}In{sub 0.094}Ce{sub 0.065}Co{sub 4}Sb{sub 11.92} at 800 K.

  4. Integrating Steel Production with Mineral Carbon Sequestration

    SciTech Connect (OSTI)

    Klaus Lackner; Paul Doby; Tuncel Yegulalp; Samuel Krevor; Christopher Graves

    2008-05-01

    The objectives of the project were (i) to develop a combination iron oxide production and carbon sequestration plant that will use serpentine ores as the source of iron and the extraction tailings as the storage element for CO2 disposal, (ii) the identification of locations within the US where this process may be implemented and (iii) to create a standardized process to characterize the serpentine deposits in terms of carbon disposal capacity and iron and steel production capacity. The first objective was not accomplished. The research failed to identify a technique to accelerate direct aqueous mineral carbonation, the limiting step in the integration of steel production and carbon sequestration. Objective (ii) was accomplished. It was found that the sequestration potential of the ultramafic resource surfaces in the US and Puerto Rico is approximately 4,647 Gt of CO2 or over 500 years of current US production of CO2. Lastly, a computer model was developed to investigate the impact of various system parameters (recoveries and efficiencies and capacities of different system components) and serpentinite quality as well as incorporation of CO2 from sources outside the steel industry.

  5. SkyMine Carbon Mineralization Pilot Project

    SciTech Connect (OSTI)

    Joe Jones; Clive Barton; Mark Clayton; Al Yablonsky; David Legere

    2010-09-30

    This Topical Report addresses accomplishments achieved during Phase 1 of the SkyMine{reg_sign} Carbon Mineralization Pilot Project. The primary objectives of this project are to design, construct, and operate a system to capture CO{sub 2} from a slipstream of flue gas from a commercial coal-fired cement kiln, convert that CO{sub 2} to products having commercial value (i.e., beneficial use), show the economic viability of the CO{sub 2} capture and conversion process, and thereby advance the technology to a point of readiness for commercial scale demonstration and proliferation. The project will also substantiate market opportunities for the technology by sales of chemicals into existing markets, and identify opportunities to improve technology performance and reduce costs at commercial scale. The primary objectives of Phase 1 of the project were to elaborate proven SkyMine{reg_sign} process chemistry to commercial pilot-scale operation and complete the preliminary design ('Reference Plant Design') for the pilot plant to be built and operated in Phase 2. Additionally, during Phase 1, information necessary to inform a DOE determination regarding NEPA requirements for the project was developed, and a comprehensive carbon lifecycle analysis was completed. These items were included in the formal application for funding under Phase 2. All Phase 1 objectives were successfully met on schedule and within budget.

  6. The estimation of the number of underground coal miners and the annual dose to coal miners in China

    SciTech Connect (OSTI)

    Liu, F.D.; Pan, Z.Q.; Liu, S.L.; Chen, L.; Ma, J.Z.; Yang, M.L.; Wang, N.P.

    2007-08-15

    This paper introduces an estimation method for the number of underground coal miners and the annual dose to coal miners in China. It shows that there are about 6 million underground miners at present and the proportion is about 1, 1 and 4 million for national key coal mines, state-owned local coal mines, and township and private-ownership coal mines, respectively. The collective dose is about 1.65 X 10{sup 4} person-Sv y{sup -1}, of which township and private-ownership coal mines contribute about 91%. This paper also points out that the 2000 UNSCEAR report gives the number of miners of coal production and their collective dose, which are underestimated greatly because the report only includes the number of underground miners in national key coal mines, which only accounts for 1/6 of the workers all working under the best ventilation conditions in China.

  7. Chemically Accelerated Carbon Mineralization: Chemical and Biological Catalytic Enhancement of Weathering of Silicate Minerals as Novel Carbon Capture and Storage

    SciTech Connect (OSTI)

    None

    2010-07-01

    IMPACCT Project: Columbia University is developing a process to pull CO2 out of the exhaust gas of coal-fired power plants and turn it into a solid that can be easily and safely transported, stored above ground, or integrated into value-added products (e.g. paper filler, plastic filler, construction materials, etc.). In nature, the reaction of CO2 with various minerals over long periods of time will yield a solid carbonatethis process is known as carbon mineralization. The use of carbon mineralization as a CO2 capture and storage method is limited by the speeds at which these minerals can be dissolved and CO2 can be hydrated. To facilitate this, Columbia University is using a unique process and a combination of chemical catalysts which increase the mineral dissolution rate, and the enzymatic catalyst carbonic anhydrase which speeds up the hydration of CO2.

  8. Lattice, Ce-L{sub 3}valence, transport, and magnetic results on mixed-valent/Kondo system Ce{sub 1{minus}x}La{sub x}Mn{sub 2}Si{sub 2}

    SciTech Connect (OSTI)

    Liang, G.; Xi, H.; Roberts, E.; Binford, T.; Mochizuki, K.; Markert, J.T.; Croft, M.

    1997-04-01

    Lattice, Ce-L{sub 3} edge, resistivity, and magnetic susceptibility measurements have been carried out on the polycrystalline Ce{sub 1{minus}x}La{sub x}Mn{sub 2}Si{sub 2} system (0{le}x{le}1) to study the interplay between Mn 3d-host magnetism and Kondo-type Ce-spin fluctuations. As x increases, the system varies gradually from a Ce mixed-valent system with 3d-host antiferromagnetism (at x=0) to a nearly trivalent system with strong 3d-host ferromagnetism (near x=1). In the antiferromagnetic (AF) phase region (0{le}x{le}0.5), the Neel temperature T{sub N} decreases with the increase of x, manifesting the weakening of the host AF field. Impurity Kondo behavior is observed at x=0.05, indicating that the low-temperature coherence state in CeMn{sub 2}Si{sub 2} can be destroyed by {open_quotes}Kondo holes{close_quotes} which are created by very small substitution of La for Ce. The susceptibility and resistivity results suggest that the impurity Kondo effect in the 0.1{le}x{le}0.5 samples is partially suppressed by a nonvanishing ferromagnetic (FM) field component; whereas the phononlike behavior of the resistivity curves in the Mn-host FM-phase region (0.5{lt}x{le}1.0) supports our previous proposal that the Kondo-type Ce-spin fluctuations can be effectively quenched by a strong 3d-host FM field. {copyright} {ital 1997 American Institute of Physics.}

  9. Assessment of industrial minerals and rocks in the controlled area

    SciTech Connect (OSTI)

    Castor, S.B.; Lock, D.E.

    1996-08-01

    Yucca Mountain in Nye County, Nevada, is a potential site for a permanent repository for high-level nuclear waste in Miocene ash flow tuff. The Yucca Mountain controlled area occupies approximately 98 km{sup 2} that includes the potential repository site. The Yucca Mountain controlled area is located within the southwestern Nevada volcanic field, a large area of Miocene volcanism that includes at least four major calderas or cauldrons. It is sited on a remnant of a Neogene volcanic plateau that was centered around the Timber Mountain caldera complex. The Yucca Mountain region contains many occurrences of valuable or potentially valuable industrial minerals, including deposits with past or current production of construction aggregate, borate minerals, clay, building stone, fluorspar, silicate, and zeolites. The existence of these deposits in the region and the occurrence of certain mineral materials at Yucca Mountain, indicate that the controlled area may have potential for industrial mineral and rock deposits. Consideration of the industrial mineral potential within the Yucca Mountain controlled area is mainly based on petrographic and lithologic studies of samples from drill holes in Yucca Mountain. Clay minerals, zeolites, fluorite, and barite, as minerals that are produced economically in Nevada, have been identified in samples from drill holes in Yucca Mountain.

  10. Kondo-lattice behavior and multiple characteristic temperatures in CeIr{sub 2}Ge{sub 2}

    SciTech Connect (OSTI)

    Mallik, R.; Sampathkumaran, E.V.; Paulose, P.L.; Dumschat, J.; Wortmann, G.

    1997-02-01

    The results of electrical-resistivity {rho} measurements (1.4{endash}300 K) on the alloys, Ce{sub 1{minus}x}La{sub x}Ir{sub 2}Ge{sub 2} (0{le}x{le}1), CeIr{sub 2{minus}x}(Rh,Pt){sub x}Ge{sub 2} (x=0.2 and 0.4), and CeIr{sub 2}Ge{sub 2{minus}x}(Si,Sn){sub x} (x=0.2 and 0.4), are reported in order to understand the Kondo effect in CeIr{sub 2}Ge{sub 2}. There is a significant decrease in {rho} as the temperature is lowered from 100 to 4.2 K for x = 0.0. This feature disappears for a small replacement of Ce by La (x = 0.3), thereby resulting in a single-ion Kondo effect for higher values of x. This finding establishes that the temperature T{sub coh}, characterizing the coherent scattering among the Kondo centers for x=0 is as large as about 100 K. The coherent scattering is not destroyed by small substitutions at the Ir or Ge site. The observed sensitivity of this coherence effect to a small disruption of Ce sublattice periodicity alone by La substitution is uncommon among trivalent Ce alloys. Such a large T{sub coh} value enables us to emphasize the need to invoke three characteristic temperatures for nonmagnetic Kondo lattices. {copyright} {ital 1997} {ital The American Physical Society}

  11. Surface-structure sensitivity of CeO2 nanocrystals in photocatalysis and enhancing the reactivity with nanogold

    SciTech Connect (OSTI)

    Lei, Wanying; Zhang, Tingting; Gu, Lin; Liu, Ping; Rodriguez, José A.; Liu, Gang; Liu, Minghua

    2015-06-19

    Structure–function correlations are a central theme in heterogeneous (photo)catalysis. In this research, using aberration-corrected scanning transmission electron microscopy (STEM), the atomic surface structures of well-defined one-dimensional (1D) CeO2 nanorods (NRs) and 3D nanocubes (NCs) are directly visualized at subangstrom resolution. CeO2 NCs predominantly expose the {100} facet, with {110} and {111} as minor cutoff facets at the respective edges and corners. Notably, the outermost surface layer of the {100} facet is nearly O-terminated. Neither surface relaxations nor reconstructions on {100} are observed, indicating unusual polarity compensation, which is primarily mediated by near-surface oxygen vacancies. The surface of CeO2 NRs is highly stepped, with the enclosed {110} facet exposing Ce cations and O anions on terraces. On the basis of STEM profile-view imaging and electronic structure analysis, the photoreactivity of CeO2 nanocrystals toward aqueous methyl orange degradation under UV is revealed to be surface-structure-sensitive, following the order: {110} >> {100}. The underlying surface-structure sensitivity can be attributed to the variation in low-coordinate surface cerium cations between {110} and {100} facets. To further enhance light absorption, Au nanoparticles (NPs) are deposited on CeO2 NRs to form Au/CeO2 plasmonic nanocomposites, which dramatically promotes the photoreactivity that is Au particle size- and excitation light wavelength-dependent. The mechanisms responsible for the enhancement of photocatalytic activity are discussed, highlighting the crucial role of photoexcited charge carrier transfer.

  12. Surface-structure sensitivity of CeO2 nanocrystals in photocatalysis and enhancing the reactivity with nanogold

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Lei, Wanying; Zhang, Tingting; Gu, Lin; Liu, Ping; Rodriguez, José A.; Liu, Gang; Liu, Minghua

    2015-06-19

    Structure–function correlations are a central theme in heterogeneous (photo)catalysis. In this research, using aberration-corrected scanning transmission electron microscopy (STEM), the atomic surface structures of well-defined one-dimensional (1D) CeO2 nanorods (NRs) and 3D nanocubes (NCs) are directly visualized at subangstrom resolution. CeO2 NCs predominantly expose the {100} facet, with {110} and {111} as minor cutoff facets at the respective edges and corners. Notably, the outermost surface layer of the {100} facet is nearly O-terminated. Neither surface relaxations nor reconstructions on {100} are observed, indicating unusual polarity compensation, which is primarily mediated by near-surface oxygen vacancies. The surface of CeO2 NRs ismore » highly stepped, with the enclosed {110} facet exposing Ce cations and O anions on terraces. On the basis of STEM profile-view imaging and electronic structure analysis, the photoreactivity of CeO2 nanocrystals toward aqueous methyl orange degradation under UV is revealed to be surface-structure-sensitive, following the order: {110} >> {100}. The underlying surface-structure sensitivity can be attributed to the variation in low-coordinate surface cerium cations between {110} and {100} facets. To further enhance light absorption, Au nanoparticles (NPs) are deposited on CeO2 NRs to form Au/CeO2 plasmonic nanocomposites, which dramatically promotes the photoreactivity that is Au particle size- and excitation light wavelength-dependent. The mechanisms responsible for the enhancement of photocatalytic activity are discussed, highlighting the crucial role of photoexcited charge carrier transfer.« less

  13. Impact of antitrust enforcement on the Country's minerals posture

    SciTech Connect (OSTI)

    Not Available

    1981-10-07

    This review found that there have not been a significant number of nonfuel-minerals-industry-related antitrust cases litigated at FTC or Justice over the last several years. In addition, officials interviewed in the nonfuel minerals industries generally do not view antitrust enforcement as a serious obstacle to their activities. The Department of Justice and FTC's Bureau of Competition comments on this report are included in enclosure II. Enclosure I presents a background discussion on antitrust enforcement, followed by detailed findings and conclusions. Enclosure III summarizes several antitrust investigations and cases cited by minerals industry spokesmen as examples of antitrust problems. (PSB)

  14. Optical properties of {gamma}- and {alpha}-Ce by spectroscopic ellipsometry

    SciTech Connect (OSTI)

    Joo Yull, Rhee

    1992-07-20

    A rotating analyzer type ellipsometer with an ultra high vacuum sample chamber was built. The dielectric functions of {gamma}- and {alpha}-Ce were measured in the energy range from 1.5 to 5.4 eV to investigate the role of the 4f electron in the isostructural phase transition. {gamma}- and {alpha}-Ce were made by evaporation of Ce on sapphire substrates at room temperature and 25 K. All measurements were performed inside a UHV chamber at pressures lower than l {times} 10{sup {minus}10}Torr. The measured dielectric functions showed a thickness dependence. The thicker sample has the smaller optical conductivities. Both overlayer thickness and void fraction increase as sample thickness increases. Repeating cooling-heating-cooling or heating-cooling-heating cycles causes the sample surface to become rougher but the relative volume fractions of both phases and the void fraction in the bulk remain unchanged. The optical conductivity increases upon entering the a-phase but the number of electrons per atom, N{sub eff}/N{sub A}, contributing to the optical conductivity does not change. The valence electrons lose oscillator strength in the above energy range due to volume collapse. This reduces N{sub eff}/NA but the increased 4f-sd valence band hybridization exactly compensates the reduced oscillator strength. Therefore the net effects of the {gamma}{yields}{alpha} isostructural phase transition are an increase of optical conductivity and constancy of N{sub eff}/N{sub A}.

  15. Structure and magnetic properties of Ba{sub 5}Ce{sub 1.25}Mn{sub 3.75}O{sub 15}, a new 10H-polytype in the Ba-Ce-Mn-O system

    SciTech Connect (OSTI)

    Macias, Mario A.; Mentre, Olivier; Cuello, Gabriel J.; Gauthier, Gilles H.

    2013-02-15

    Based on the peculiar magnetic properties that are observed in pseudo one-dimensional manganites, we decided to synthesize the new Ba{sub 5}Ce{sub 1.25}Mn{sub 3.75}O{sub 15} compound. The preparation was performed by solid state reaction in air at about 1350 Degree-Sign C, for which we found that the compound crystallizes in a hexagonal symmetry with space group P6{sub 3}/mmc (No-194) and cell parameters a=b=5.7861(2) A and c=23.902(1) A. The structural description was correlated with neutron diffraction and bond valence calculations, confirming the presence of Ce{sup 4+} and Mn{sup 4+} segregated in the different crystallographic positions. Ba{sub 5}Ce{sub 1.25}Mn{sub 3.75}O{sub 15} displays evidence for strong AFM couplings already set at room temperature. The main arrangement of Mn{sup 4+} in magnetically isolated tetramers of face-sharing octahedra is responsible for a metamagnetic-like transition around 50 K. - Graphical abstract: The new Ba{sub 5}Ce{sub 1.25}Mn{sub 3.75}O{sub 15} polytype shows strong AFM couplings in magnetically isolated [Ce{sub 0.25}Mn{sub 3.75}O{sub 15}] tetramers of face-sharing octahedral, resulting in a metamagnetic-like transition around 50 K. Highlights: Black-Right-Pointing-Pointer Ba{sub 5}Ce{sub 1.25}Mn{sub 3.75}O{sub 15}, a new 10H polytype, has been prepared in the Ba-Ce-Mn-O system. Black-Right-Pointing-Pointer The compound crystallizes in the P6{sub 3}/mmc space group with (cchhh){sub 2} stacking sequence. Black-Right-Pointing-Pointer [Ce{sub 0.25}Mn{sub 3.75}O{sub 15}] tetramers are separated by [CeO{sub 6}] octahedra in the structure. Black-Right-Pointing-Pointer Instead of robust AFM ordering, a metamagnetic-like transition is found around 50 K.

  16. Disorder and size effects on Kondo interactions and magneticcorrelations in CePt2 nanoscrystals

    SciTech Connect (OSTI)

    Chen, Y.Y.; Huang, P.H.; Ou, M.N.; Wang, C.R.; Yao, Y.D.; Lee,T.K.; Ho, M.Y.; Lawrence, J.M.; Booth, C.H.

    2006-12-12

    The evolution of the Kondo effect and magnetic correlations with size reduction in CePt{sub 2} nanoparticles (3.1-26 nm) is studied by analysis of the temperature-dependent specific heat and magnetic susceptibility. The antiferromagnetic correlations diminish with size reduction. The Kondo effect predominates at small particle size with trivalent, small Kondo temperature (T{sub K}) magnetic regions coexisting with strongly mixed valent, large T{sub K} nonmagnetic regions. We discuss the role of structural disorder, background density of states and the electronic quantum size effect on the results.

  17. Nanostructured LaF{sub 3}:Ce Quantum Dot Nuclear Radiation Detector

    SciTech Connect (OSTI)

    Guss, P., Guise, R., Reed, M., Mukhopadhyay, S., Yuan, D.

    2010-11-01

    Many radioactive isotopes have low energy X-rays and high energy gamma rays of interest for detection. The goal of the work presented was to demonstrate the possibility of measuring both low-energy X-rays and relatively high-energy gamma rays simultaneously using the nano-structured lanthanum bromide, lanthanum fluoride, or cerium bromide. The key accomplishments of the project was the building and acquisition of the LaF3:Ce nanocomposite detectors. Nanocomposite detectors are sensitive to {gamma}s as well as ns and X-rays.

  18. Neutron Scattering of CeNi at the SNS-ORNL: A Preliminary Report

    Office of Scientific and Technical Information (OSTI)

    (Conference) | SciTech Connect SNS-ORNL: A Preliminary Report Citation Details In-Document Search Title: Neutron Scattering of CeNi at the SNS-ORNL: A Preliminary Report Authors: Mirmelstein, A V ; Podlesnyak, A ; Kolesnikov, A I ; Saporov, B ; Sefat, A S ; Tobin, J G Publication Date: 2014-04-13 OSTI Identifier: 1132013 Report Number(s): LLNL-PROC-653272 DOE Contract Number: DE-AC52-07NA27344 Resource Type: Conference Resource Relation: Conference: Presented at: 2014 Materials Research

  19. Analysis of FEL-based CeC amplification at high gain limit

    SciTech Connect (OSTI)

    Wang, G.; Litvinenko, V.; Jing, Y.

    2015-05-03

    An analysis of Coherent electron Cooling (CeC) amplifier based on 1D Free Electron Laser (FEL) theory was previously performed with exact solution of the dispersion relation, assuming electrons having Lorentzian energy distribution. At high gain limit, the asymptotic behavior of the FEL amplifier can be better understood by Taylor expanding the exact solution of the dispersion relation with respect to the detuning parameter. In this work, we make quadratic expansion of the dispersion relation for Lorentzian energy distribution and investigate how longitudinal space charge and electrons’ energy spread affect the FEL amplification process.

  20. DOE 10 CFR Parts 430 and 431, Docket No. EERE-2010-BT-CE-0014 RIN

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    1904-AC23, Federal Register Vol. 75, No. 88, 25121-24 (Friday, May 7, 2010), Revisions to Energy Efficiency Enforcement Regulations, Request for Information (RFI);request for comm | Department of Energy Parts 430 and 431, Docket No. EERE-2010-BT-CE-0014 RIN 1904-AC23, Federal Register Vol. 75, No. 88, 25121-24 (Friday, May 7, 2010), Revisions to Energy Efficiency Enforcement Regulations, Request for Information (RFI);request for comm DOE 10 CFR Parts 430 and 431, Docket No.

  1. Pulse studies to decipher the role of surface morphology in CuO/CeO₂ nanocatalysts for the water gas shift reaction

    SciTech Connect (OSTI)

    Rodriguez, Jose A.; Zhao, Fuzhen; Liu, Zongyuan; Xu, Wenqian; Yao, Siyu; Si, Rui; Johnston-Peck, Aaron C.; Martinez-Arias, Arturo; Hanson, Jonathan C.; Senanayake, Sanjaya D.

    2015-01-23

    The water-gas shift reaction (WGS, CO + H₂O → CO₂) was studied over CuO/CeO₂ catalysts with two different ceria particle morphohologies, in the form of nanospheres (ns) and nanocubes (nc). To understand the strong dependence of the WGS reaction activity on the ceria nanoshapes, pulses of CO (without and with water vapor) were employed during in situ X-ray diffraction (XRD) and X-ray absoprtion near edge structure (XANES) measurements done to characterize the catalysts. The results showed that CuO/CeO₂ (ns) exhibited a substantially better activity than CuO/CeO₂ (nc). The higher activity was associated with the unique properties of CuO/CeO₂ (ns), such as the easier reduction of highly dispersed CuO to metallic Cu, the stability of metallic Cu and a larger concentration Ce³⁺ in CeO₂ (ns).

  2. Pulse studies to decipher the role of surface morphology in CuO/CeO₂ nanocatalysts for the water gas shift reaction

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Rodriguez, Jose A.; Zhao, Fuzhen; Liu, Zongyuan; Xu, Wenqian; Yao, Siyu; Si, Rui; Johnston-Peck, Aaron C.; Martinez-Arias, Arturo; Hanson, Jonathan C.; Senanayake, Sanjaya D.

    2015-01-23

    The water-gas shift reaction (WGS, CO + H₂O → CO₂) was studied over CuO/CeO₂ catalysts with two different ceria particle morphohologies, in the form of nanospheres (ns) and nanocubes (nc). To understand the strong dependence of the WGS reaction activity on the ceria nanoshapes, pulses of CO (without and with water vapor) were employed during in situ X-ray diffraction (XRD) and X-ray absoprtion near edge structure (XANES) measurements done to characterize the catalysts. The results showed that CuO/CeO₂ (ns) exhibited a substantially better activity than CuO/CeO₂ (nc). The higher activity was associated with the unique properties of CuO/CeO₂ (ns), suchmore » as the easier reduction of highly dispersed CuO to metallic Cu, the stability of metallic Cu and a larger concentration Ce³⁺ in CeO₂ (ns).« less

  3. Fundamental study of CO2-H2O-mineral interactions for carbon...

    Office of Scientific and Technical Information (OSTI)

    sequestration, with emphasis on the nature of the supercritical fluid-mineral interface. ... sequestration, with emphasis on the nature of the supercritical fluid-mineral interface. ...

  4. H.R.S. 182-1 - Reservation and Disposition of Government Mineral...

    Open Energy Info (EERE)

    Government Mineral Rights, DefinitionsLegal Abstract Hawaii statute governing the administration of government mineral rights, including rights for geothermal resources. Published...

  5. Evolution of a Mineralized Geothermal System, Valles Caldera...

    Open Energy Info (EERE)

    Journal Article: Evolution of a Mineralized Geothermal System, Valles Caldera, New Mexico Abstract The 20-km-diam Valles caldera formed at 1.13 Ma and had continuous...

  6. A Review Of Water Contents Of Nominally Anhydrous Natural Minerals...

    Open Energy Info (EERE)

    Of Water Contents Of Nominally Anhydrous Natural Minerals In The Mantles Of Earth, Mars And The Moon Jump to: navigation, search OpenEI Reference LibraryAdd to library Journal...

  7. ORS 516 - Department of Geology and Mineral Industries | Open...

    Open Energy Info (EERE)

    6 - Department of Geology and Mineral Industries Jump to: navigation, search OpenEI Reference LibraryAdd to library Legal Document- StatuteStatute: ORS 516 - Department of Geology...

  8. Mercury Contents of Natural Thermal and Mineral Fluids, In- U...

    Open Energy Info (EERE)

    Paper 713 Jump to: navigation, search OpenEI Reference LibraryAdd to library Book Section: Mercury Contents of Natural Thermal and Mineral Fluids, In- U.S. Geological...

  9. Hyperspectral Mineral Mapping In Support Of Geothermal Exploration...

    Open Energy Info (EERE)

    Ca And Dixie Valley, Nv, Usa Jump to: navigation, search OpenEI Reference LibraryAdd to library Book: Hyperspectral Mineral Mapping In Support Of Geothermal Exploration- Examples...

  10. Nickel deficiency in RENi2-xP2 (RE=La, Ce, Pr). Combined crystallographic and physical property studies

    SciTech Connect (OSTI)

    Bauer, Eric D; Ronning, Filip; Thompson, Joe D; Sarrao, John L; Bobev, S; Xia, S

    2008-01-01

    Large single crystals from RENi{sub 2-x}P{sub 2} (RE = La, Ce, Pr) were synthesized from the pure elements using Sn as a metal flux, and their structures were established by X-ray crystallography. The title compounds were confirmed to crystallize in the body-centered tetragonal ThCr{sub 2}Si{sub 2} structure type (space group I4/mmm (No. 139); Pearson's symbol tI10), but with a significant stoichiometry breadth with respect to the transition metal. Systematic synthetic work, coupled with accurate structure refinements indicated strong correlation between the degree of Ni-deficiency and the reaction conditions. For four different PrNi{sub 2-x}P{sub 2} (x {le} 0.5) samples, temperature dependent dc magnetization measurements indicated typical local moment 4f-magnetism and a stable Pr{sup 3+} ground state. Field-dependent heat capacity data confirmed a ferromagnetic order at low temperature, and the variations of T{sub c} with the concentration of Ni defects are discussed. LaNi{sub 2-x}P{sub 2}, as expected was found to be Pauli-like paramagnetic in the studied temperature regime, while the Ce-analog CeNi{sub 2-x}P{sub 2} (x = 0.28(1)) showed the characteristics of a mixed valent Ce{sup 3+}/Ce{sup 4+} system with a possible Kondo temperature on the order of 230 K.

  11. Underground radio technology saves miners and emergency response personnel

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Underground radio technology saves miners and emergency response personnel Underground radio technology saves miners and emergency response personnel Founded through LANL, Vital Alert Technologies, Inc. (Vital Alert) has launched a wireless, two-way real-time voice communication system that is effective through 1,000+ feet of solid rock. April 3, 2012 Vital Alert's C1000 mine and tunnel radios use magnetic induction, advanced digital communications techniques and ultra-low frequency transmission

  12. Molecular Simulation of Carbon Dioxide Brine and Clay Mineral Interactions

    Office of Scientific and Technical Information (OSTI)

    and Determination of Contact Angles. (Journal Article) | SciTech Connect Journal Article: Molecular Simulation of Carbon Dioxide Brine and Clay Mineral Interactions and Determination of Contact Angles. Citation Details In-Document Search Title: Molecular Simulation of Carbon Dioxide Brine and Clay Mineral Interactions and Determination of Contact Angles. Abstract not provided. Authors: Tenney, Craig M ; Cygan, Randall T. Publication Date: 2013-08-01 OSTI Identifier: 1106710 Report Number(s):

  13. Diagenesis and clay mineral formation at Gale Crater, Mars (Journal

    Office of Scientific and Technical Information (OSTI)

    Article) | SciTech Connect Journal Article: Diagenesis and clay mineral formation at Gale Crater, Mars Citation Details In-Document Search Title: Diagenesis and clay mineral formation at Gale Crater, Mars × You are accessing a document from the Department of Energy's (DOE) SciTech Connect. This site is a product of DOE's Office of Scientific and Technical Information (OSTI) and is provided as a public service. Visit OSTI to utilize additional information resources in energy science and

  14. A highly conspicuous mineralized composite photonic architecture in the

    Office of Scientific and Technical Information (OSTI)

    translucent shell of the blue-rayed limpet (Journal Article) | DOE PAGES A highly conspicuous mineralized composite photonic architecture in the translucent shell of the blue-rayed limpet « Prev Next » Title: A highly conspicuous mineralized composite photonic architecture in the translucent shell of the blue-rayed limpet × You are accessing a document from the Department of Energy's (DOE) Public Access Gateway for Energy & Science (PAGES). This site is a product of DOE's Office of

  15. Mineral Deformation at Earth's Core-Mantle Boundary

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Mineral Deformation at Earth's Core-Mantle Boundary Mineral Deformation at Earth's Core-Mantle Boundary Print Wednesday, 31 August 2011 00:00 Earth is a dynamic planet in which convection takes place on the scale of thousands of kilometers. Because Earth is mostly solid (except for its liquid-iron outer core), this convection causes deformation of solid rocks by plastic flow. At the core-mantle boundary (CMB), 2900 km deep, seismologists have discovered that seismic waves travel faster in

  16. Thermodynamic stability of actinide pyrochlore minerals in deep geologic

    Office of Scientific and Technical Information (OSTI)

    repository environments (Conference) | SciTech Connect Thermodynamic stability of actinide pyrochlore minerals in deep geologic repository environments Citation Details In-Document Search Title: Thermodynamic stability of actinide pyrochlore minerals in deep geologic repository environments Crystalline phases of pyrochlore (e.g., CaPuTi{sub 2}O{sub 7}, CaUTi{sub 2}O{sub 7}) have been proposed as a durable ceramic waste form for disposal of high level radioactive wastes including surplus

  17. Request for Information explores mineral recovery from geothermal fluids |

    Energy Savers [EERE]

    Department of Energy Request for Information explores mineral recovery from geothermal fluids Request for Information explores mineral recovery from geothermal fluids May 12, 2015 - 11:01am Addthis Geothermal energy below the boiling point is now being harnessed to generate electricity and a host of applications. Source: NREL/Ted Clutter Geothermal energy below the boiling point is now being harnessed to generate electricity and a host of applications. Source: NREL/Ted Clutter The DOE

  18. Low-Temperature Mineral Recovery Program FOA Selections | Department of

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Energy Temperature Mineral Recovery Program FOA Selections Low-Temperature Mineral Recovery Program FOA Selections This early exploration well, drilled in Montana to find oil, has yielded over 1000 gallons per minute of hot goethermal fluid. The Energy Department is finding new ways to tap these natural energy streams to generate power and a number of direct use applications. Source: Geothermal Resources Council This early exploration well, drilled in Montana to find oil, has yielded over

  19. Mineral Recovery Creates Revenue Stream for Geothermal Energy Development |

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    Department of Energy Mineral Recovery Creates Revenue Stream for Geothermal Energy Development Mineral Recovery Creates Revenue Stream for Geothermal Energy Development December 1, 2015 - 8:00am Addthis Critical materials like rare-earth elements and lithium play a vital role in many clean-energy technologies, including solar panels, wind turbines, electric vehicles, and energy-saving lighting. The Energy Department is pursuing a range of research and development efforts to secure and

  20. DOE - Office of Legacy Management -- Foote Mineral Co - PA 27

    Office of Legacy Management (LM)

    Foote Mineral Co - PA 27 FUSRAP Considered Sites Site: Foote Mineral Co. (PA.27 ) Eliminated from further consideration under FUSRAP Designated Name: Not Designated Alternate Name: None Location: Exton , Pennsylvania PA.27-1 Evaluation Year: 1987 PA.27-1 Site Operations: Processed rare earth, principally zirconium and monazite sand was processed on a pilot-plant scale. PA.27-2 Site Disposition: Eliminated - Limited quantity of material handled - Potential for contamination considered remote

  1. Theoretical Study of Trimethylacetic Acid Adsorption on CeO 2 (111) Surface

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Wang, Weina; Thevuthasan, S.; Wang, Wenliang; Yang, Ping

    2016-01-11

    We investigated trimethylacetic acid (TMAA) adsorption on stoichiometric and oxygen-deficient CeO2(111) surfaces using density functional theory that accounts for the on-site Coulomb interaction via a Hubbard term (DFT+U) and long-range dispersion correction. Both the molecular state and dissociative state (TMAA → TMA– + H+) were identified on stoichiometric and oxygen-deficient CeO2(111) surfaces. For the stoichiometric surface, two thermodynamically favorable configurations with adsorption energies of the order of -30 kcal/mol are identified; one is a molecule adsorption state, and the other one is a dissociative state. For the oxygen-deficient surface, dissociative states are more favorable than molecular states. Moreover, the mostmore » favorable configuration is the dissociative adsorption of TMAA with the adsorption energy of the order of -77 kcal/mol. The dissociated TMA moiety takes the position of oxygen vacancy, forming three Ce–O bonds. The signature vibrational frequencies for these thermodynamically stable structures are reported as well as their electronic structures. The effects of long-range dispersion interactions are found to be negligible for geometries but important for adsorption energies.« less

  2. Electronic structure of the heavy-fermion caged compound Ce?Pd??X? (X = Si, Ge) studied by density functional theory and photoelectron spectroscopy

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Yamaoka, Hitoshi; Jarrige, Ignace; Schwier, Eike F.; Arita, Masashi; Shimada, Kenya; Tsujii, Naohito; Jiang, Jian; Hayashi, Hirokazu; Iwasawa, Hideaki; Namatame, Hirofumi; et al

    2015-03-30

    The electronic structure of Ce?Pd??X? (X = Si, Ge) has been studied using detailed density functional theory (DFT) calculations and high-resolution photoelectron spectroscopy (PES) measurements. The orbital decomposition of the electronic structure by DFT calculations indicates that Ce atoms at the (8c) site surrounded by 16 Pd atoms have a more localized nature and a tendency to be magnetic. Ce atoms in the (4a) site surrounded by 12 Pd and 6 X atoms, on the other, show only a negligible magnetic moment. In the photoemission valence-band spectra we observe a strong f? (Ce??) component with a small fraction of fmore(Ce?) component. The spectral weight of f component near the Fermi level Ce?Pd??Si? is stronger than that for Ce?Pd??Ge? at the 4d-4f resonance, suggesting stronger c-f hybridization in the former. This may hint to the origin of the large electronic specific coefficient of Ce?Pd??Si? compared to Ce?Pd??Ge?.less

  3. Influence of solvent on the morphology and photocatalytic properties of ZnS decorated CeO{sub 2} nanoparticles

    SciTech Connect (OSTI)

    Raubach, Cristiane W. Polastro, Lisnias; Ferrer, Mateus M.; Perrin, Andre; Perrin, Christiane; Albuquerque, Anderson R.; Buzolin, Prescila G. C.; Sambrano, Julio R.; Santana, Yuri B. V. de; Varela, Jos A.; Longo, Elson

    2014-06-07

    Herein, we report a theoretical and experimental study on the photocatalytic activity of CeO{sub 2} ZnS, and ZnS decorated CeO{sub 2} nanoparticles prepared by a microwave-assisted solvothermal method. Theoretical models were established to analyze electron transitions primarily at the interface between CeO{sub 2} and ZnS. As observed, the particle morphology strongly influenced the photocatalytic degradation of organic dye Rhodamine B. A model was proposed to rationalize the photocatalytic behavior of the prepared decorated systems taking into account different extrinsic and intrinsic defect distributions, including order-disorder effects at interfacial and intra-facial regions, and vacancy concentration.

  4. Temperature Dependence of the Kondo Resonance and Its Satellites in CeCu{sub 2}Si{sub 2}

    SciTech Connect (OSTI)

    Reinert, F.; Ehm, D.; Schmidt, S.; Nicolay, G.; Huefner, S.; Kroha, J.; Trovarelli, O.; Geibel, C.

    2001-09-03

    We present high-resolution photoemission spectroscopy studies on the Kondo resonance of the strongly correlated Ce system CeCu{sub 2}Si {sub 2} . By exploiting the thermal broadening of the Fermi edge we analyze position, spectral weight, and temperature dependence of the low-energy 4f spectral features, whose major weight lies above the Fermi level E{sub F} . We also present theoretical predictions based on the single-impurity Anderson model using an extended noncrossing approximation, including all spin-orbit and crystal field splittings of the 4f states. The excellent agreement between theory and experiment provides strong evidence that the spectral properties of CeCu{sub 2}Si {sub 2} can be described by single-impurity Kondo physics down to T{approx}5 K .

  5. Update on the CeC PoP 704 MHz 5-cell cavity cryomodule design and fabrication

    SciTech Connect (OSTI)

    Brutus, J. C.; Belomestnykh, S.; Ben-Zvi, I.; Grimm, T.; Huang, Y.; Jecks, R.; Kelly, M.; Litvinenko, V.; Pinayev, I.; Reid, T.; Skaritka, J.; Snydstrup, L.; Than, R.; Tuozzolo, J.; Xu, W.; Yancey, J.; Gerbick, S.

    2015-05-03

    A 5-cell SRF cavity operating at 704 MHz will be used for the Coherent Electron Cooling Proof of Principle (CeC PoP) system under development for the Relativistic Heavy Ion Collider (RHIC) at Brookhaven National Laboratory. The CeC PoP experiment will demonstrate the new technique of cooling proton and ion beams that may increase the beam luminosity in certain cases, by as much as tenfold. The 704 MHz cavity will accelerate 2 MeV electrons from a 112 MHz SRF gun up to 22MeV. This paper provides an overview of the design, the project status and schedule of the 704 MHz 5-cell SRF for CeC PoP experiment.

  6. 6450-01-P, DOE 10 CFR Parts 430 and 431, Docket No. EERE-2010-BT-CE-0014

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    RIN 1904-AC23, Draft Submission to Federal Register, Notice of Revisions to Energy Efficiency Enforcement Regulations, Request for Information/comment. | Department of Energy 6450-01-P, DOE 10 CFR Parts 430 and 431, Docket No. EERE-2010-BT-CE-0014 RIN 1904-AC23, Draft Submission to Federal Register, Notice of Revisions to Energy Efficiency Enforcement Regulations, Request for Information/comment. 6450-01-P, DOE 10 CFR Parts 430 and 431, Docket No. EERE-2010-BT-CE-0014 RIN 1904-AC23, Draft

  7. Determination of the Surface Structure of CeO2(111) by Low-Energy Electron

    Office of Scientific and Technical Information (OSTI)

    Diffraction. (Journal Article) | SciTech Connect Determination of the Surface Structure of CeO2(111) by Low-Energy Electron Diffraction. Citation Details In-Document Search Title: Determination of the Surface Structure of CeO2(111) by Low-Energy Electron Diffraction. Abstract not provided. Authors: McCarty, Kevin F. ; Siegel, David A ; El Gabaly Marquez, Farid ; Chueh, William ; de la Figuera, Juan ; Blanco-Rey, Maria Publication Date: 2013-06-01 OSTI Identifier: 1113313 Report Number(s):

  8. LOW TEMPERATURE GEOTHERMAL MINERAL RECOVERY PROGRAM 02/11/2014 | Department

    Office of Environmental Management (EM)

    of Energy LOW TEMPERATURE GEOTHERMAL MINERAL RECOVERY PROGRAM 02/11/2014 LOW TEMPERATURE GEOTHERMAL MINERAL RECOVERY PROGRAM 02/11/2014 PDF icon mineral-webinar.pdf More Documents & Publications LOW TEMPERATURE GEOTHERMAL MINERAL RECOVERY PROGRAM Geothermal Play Fairway Analysis Geothermal Play Fairway Analysis

  9. Diagenesis and clay mineral formation at Gale Crater, Mars

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Bridges, J. C.; Schwenzer, S. P.; Leveille, R.; Westall, F.; Wiens, R. C.; Mangold, N.; Bristow, T.; Edwards, P.; Berger, G.

    2015-01-18

    The Mars Science Laboratory rover Curiosity found host rocks of basaltic composition and alteration assemblages containing clay minerals at Yellowknife Bay, Gale Crater. On the basis of the observed host rock and alteration minerals, we present results of equilibrium thermochemical modeling of the Sheepbed mudstones of Yellowknife Bay in order to constrain the formation conditions of its secondary mineral assemblage. Building on conclusions from sedimentary observations by the Mars Science Laboratory team, we assume diagenetic, in situ alteration. The modeling shows that the mineral assemblage formed by the reaction of a CO₂-poor and oxidizing, dilute aqueous solution (Gale Portage Water)more » in an open system with the Fe-rich basaltic-composition sedimentary rocks at 10–50°C and water/rock ratio (mass of rock reacted with the starting fluid) of 100–1000, pH of ~7.5–12. Model alteration assemblages predominantly contain phyllosilicates (Fe-smectite, chlorite), the bulk composition of a mixture of which is close to that of saponite inferred from Chemistry and Mineralogy data and to that of saponite observed in the nakhlite Martian meteorites and terrestrial analogues. To match the observed clay mineral chemistry, inhomogeneous dissolution dominated by the amorphous phase and olivine is required. We therefore deduce a dissolving composition of approximately 70% amorphous material, with 20% olivine, and 10% whole rock component.« less

  10. Magnetic structure of the antiferromagnetic Kondo lattice compounds CeRhAl4Si2 and CeIrAl4Si2

    SciTech Connect (OSTI)

    Ghimire, N. J.; Calder, S.; Janoschek, M.; Bauer, E. D.

    2015-06-01

    In this article, we have investigated the magnetic ground state of the antiferromagnetic Kondo-lattice compounds CeMAl4Si2(M = Rh, Ir) using neutron powder diffraction. Although both of these compounds show two magnetic transitions TN1 and TN2 in the bulk properties measurements, evidence for magnetic long-range order was only found below the lower transition TN2. Analysis of the diffraction profiles reveals a commensurate antiferromagnetic structure with a propagation vector k = (0, 0, 1/2). The magnetic moment in the ordered state of CeRhAl4Si2 and CeIrAl4Si2 were determined to be 1.14(2) and 1.41(3) ?B/Ce, respectively, and are parallel to the crystallographic c-axis in agreement with magnetic susceptibility measurements.

  11. Vortex Lattice Studies in CeCoIn₅ with H⊥c

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Das, P.; White, J. S.; Holmes, A. T.; Gerber, S.; Forgan, E. M.; Bianchi, A. D.; Kenzelmann, M.; Zolliker, M.; Gavilano, J. L.; Bauer, E. D.; et al

    2012-02-23

    We present small angle neutron scattering studies of the vortex lattice (VL) in CeCoIn₅ with magnetic fields applied parallel (H) to the antinodal [100] and nodal [110] directions. For H II 100], a single VL orientation is observed, while a 90° reorientation transition is found for H II [110]. For both field orientations and VL configurations we find a distorted hexagonal VL with an anisotropy, Γ=2.0±0.05. The VL form factor shows strong Pauli paramagnetic effects similar to what have previously been reported for H II [001]. At high fields, above which the upper critical field (Hc2) becomes a first-order transition,more »an increased disordering of the VL is observed.« less

  12. Nanostructured Lanthanum Halides and CeBr3 for Nuclear Radiation and Detection

    SciTech Connect (OSTI)

    Paul Guss, Sanjoy Mukhopadhyay, Ron Guise, Ding Yuan

    2010-06-09

    Scintillator materials are used to detect, and in some cases identify, gamma rays. Higher performance scintillators are expensive, hard to manufacture, fragile, and sometimes require liquid nitrogen or cooling engines. But whereas lower-quality scintillators are cheap, easy to manufacture, and more rugged, their performance is lower. At issue: can the desirable qualities of high-and low-performance scintillators be combined to achieve better performance at lower cost? Preliminary experiments show that a LaF{sub 3}:Ce oleic acid-based nanocomposite exhibits a photopeak when exposed to {sup 137}Cs source gamma-radiation. The chemical synthesis of the cerium-doped lanthanum halide nanoparticles are scalable and large quantities of material can be produced at a time, unlike typical crystal growth processes such as the Bridgeman process. Using a polymer composite (Figure 1), produced by LANL, initial measurements of the unloaded and 8% LaF{sub 3}:Ce-loaded sample have been made using {sup 137}Cs sources. Figure 2 shows an energy spectrum acquired for CeF{sub 3}. The lighter plot is the measured polymer-only spectrum and the black plot is the spectrum from the nanocomposite scintillator. As the development of this material continues, the energy resolution is expected to improve and the photopeak-to-Compton ratio will become greater at higher loadings. These measurements show the expected Compton edge in the polymer-only sample, and the Compton edge and photo-peak expected in the nanophosphor composites that LANL has produced. Using a porous VYCORR with CdSe/ZnS core shell quantum dots, Letant has demonstrated that he has obtained signatures of the 241Am photopeak with energy resolution as good at NaI (Figure 3). We begin with the fact that CeBr{sub 3} crystals do not have a self-activity component as strong as the lanthanum halides. The radioactive 0.090% {sup 138}La component of lanthanum leads to significant self-activity, which will be a problem for very large detector volumes. Yet a significant strength of the nanostructure detector concept is the ability to create extremely large detector volumes by mixing nanoparticles into a transparent matrix. This would argue for use of nanoparticles other than lanthanum halides. Nanocomposites are easy to prepare; it is much less costly to use nanocomposites than to grow large whole crystals of these materials. The material can be fabricated at an industrial scale, further reducing cost. This material potentially offers the performance of $300/cc material (e.g., lanthanum bromide) at a cost of $1/cc. Because the material acts as a plastic, it is rugged and flexible, and can be made in large sheets, increasing the sensitivity of a detector using it. It would operate at ambient temperatures. Very large volumes of detector may be produced at greatly reduced cost, enhancing the non-proliferation posture of the nation for the same dollar value.

  13. Transport properties of Ce{sub 2}Ni{sub 2}Sn and Ce{sub 2}Pd{sub 2.05}Sn{sub 0.95} Kondo lattice systems

    SciTech Connect (OSTI)

    Pinto, R.P.; Amado, M.M.; Braga, M.E.; de Azevedo, M.M.; Sousa, J.B.; Chevalier, B.; Etourneau, J.

    1997-04-01

    We report experimental data on thermoelectric power S, electrical resistivity {rho}, and the magnetoresistivity of the antiferromagnet Kondo stannides Ce{sub 2}Ni{sub 2}Sn (T{sub N}=4.7 K) and Ce{sub 2}Pd{sub 2.05}Sn{sub 0.95} (T{sub N}=4.7 K). The essential features of the S(T) curves resemble those of heavy fermion systems such as CeCu{sub 2}Si{sub 2}: a broad and positive maximum at intermediate temperatures, followed by a sharper negative minimum at lower temperatures. S values are is considerably smaller in Ce{sub 2}Pd{sub 2.05}Sn{sub 0.95} than in Ce{sub 2}Ni{sub 2}Sn. The positive peak originates from the incoherent Kondo scattering by the excited crystal field levels of the Ce ion ground state. The negative peak might be related to the shape of the density of states associated with the Abrikosov{endash}Suhl resonance. The change of sign in S(T) between its minimum and maximum at T{sup {asterisk}} can be assigned to the fact that the Fermi level sinks below the upper band at T{gt}T{sup {asterisk}}. This behavior and the maximum observed in the {rho}(T) curve at this temperature can be discussed in terms of the electron polaron model, although one must also take into account the crystal field effect. The role played by the crystal field effect, which is more important in Ce{sub 2}Pd{sub 2.05}Sn{sub 0.95}, is analyzed for this compound, providing the magnitude of the crystal field splitting. Magnetoresistivity was also measured in both compounds. The results are consistent with the important role of the Kondo effect at low temperatures and suggest the splitting of the double degenerate bands at T{gt}T{sup {asterisk}}. {copyright} {ital 1997 American Institute of Physics.}

  14. The effect of Au and Ni doping on the heavy fermion state of the Kondo lattice antiferromagnet CePtZn

    SciTech Connect (OSTI)

    Dhar, S. K.; Aoki, Y.; Suemitsu, B.; Miyazaki, R.; Provino, A.; Manfrinetti, P.

    2014-05-07

    We have probed the effect of doping CePtZn with Au and Ni and also investigated in detail the magnetic behavior of the iso-structural CeAuZn. A magnetic ground state is observed in both CePt{sub 0.9}Au{sub 0.1}Zn and CePt{sub 0.9}Ni{sub 0.1}Zn with T{sub N}?=?2.1 and 1.1?K and the coefficient of the linear term of electronic heat capacity ??=?0.34 and 0.9?J/mol K{sup 2}, respectively. The corresponding values for CePtZn are 1.7?K and 0.6?J/mol K{sup 2}. The altered values of T{sub N} and ? show that the electronic correlations in CePtZn are affected by doping with Au and Ni. CeAuZn orders magnetically near 1.7?K and its electrical resistivity shows a normal metallic behavior. Together with a ? of 0.022?J/mol K{sup 2} the data indicate a weak 4f-conduction electron hybridization in CeAuZn characteristic of normal trivalent cerium based systems.

  15. Improved thermoelectric performance of n-type Ca and Ca-Ce filled skutterudites

    SciTech Connect (OSTI)

    Thompson, Daniel R.; Liu, Chang; Ellison, Nicole D.; Salvador, James R.; Meyer, Martin S.; Haddad, Daad B.; Wang, Hsin; Cai, W.

    2014-12-28

    Thermoelectric (TE) technology for use in automotive waste heat recovery is being advanced by General Motors with support from the US Department of Energy. Skutterudites are a very promising material for this application of TE technology due to their superior mechanical properties and good TE performance. Double-filled Yb{sub x}Ba{sub y}Co{sub 4}Sb{sub 12} with ZT values around 1.1 at 750?K are the best performing n-type skutterudites produced on a large scale using an economically viable approach of melt spinning (MS) in conjunction with spark plasma sintering (SPS). Another economical production method on the tons scale, the melt quench annealing (MQA) technique, has been recently claimed by Treibacher Industrie AG, further information is available [G. Rogl et al., Acta Mater. 76, 434448 (2014)]. A possible hurdle to commercial implementation of these materials is the use of rare earths as the fillers to reduce thermal conductivity and improve the electrical transport properties. It will be shown herein that skutterudites double-filled with Ca and Ce, both of which are lower-cost fillers, display markedly different TE properties depending on whether they are produced by MQA or MS + SPS synthesis techniques. Ca and Ce double-filled skutterudites prepared by MS + SPS have TE properties that are superior to the same compositions prepared by MQA and that are comparable to the best performing Yb and Ba filled materials. Furthermore, the results of this study suggest that the unusually poor transport properties of MQA Ca-filled skutterudites can be ascribed to deleterious secondary phases, which is contrary to reports in the literature attempting to explain these irregularities via band structure features.

  16. "Terrywallaceite" now in official roster of known minerals

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    » June » "Terrywallaceite" Now In Official Roster Of Known Minerals "Terrywallaceite" now in official roster of known minerals The slender, needle-like metallic-black crystals of Terrywallaceite were found in the Julcani Mining District of Peru. June 8, 2011 The mineral "Terrywallaceite" The mineral "Terrywallaceite" I am honored and humbled that a group of geoscientists and peers would suggest naming a mineral after me and that the international

  17. An active atmospheric methane sink in high Arctic mineral cryosols

    SciTech Connect (OSTI)

    Lau, Maggie C.Y.; Stackhouse, B.; Layton, Alice C.; Chauhan, Archana; Vishnivetskaya, T. A.; Chourey, Karuna; Mykytczuk, N. C.S.; Bennett, Phil C.; Lamarche-Gagnon, G.; Burton, N.; Renholm, J.; Hettich, R. L.; Pollard, W. H.; Omelon, C. R.; Medvigy, David M.; Pffifner, Susan M.; Whyte, L. G.; Onstott, T. C.

    2015-04-14

    The transition of Arctic carbon-rich cryosols into methane (CH?)-emitting wetlands due to global warming is a rising concern. However, the spatially predominant mineral cryosols and their CH? emission potential are poorly understood. Fluxes measured in situ and estimated under laboratory conditions coupled with -omics analysis indicate (1) mineral cryosols in the Canadian high Arctic contain atmospheric CH?-oxidizing bacteria; (2) the atmospheric CH? uptake flux increases with ground temperature; and, as a result, (3) the atmospheric CH? sink strength will increase by a factor of 5-30 as the Arctic warms by 5-15 C over a century. We demonstrated that acidic mineral cryosols have previously unrecognized potential of negative CH? feedback.

  18. Investigation of the physical properties of the tetragonal CeMAl4Si2 (M = Rh, Ir, Pt) compounds

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Ghimire, N. J.; Ronning, F.; Williams, D. J.; Scott, B. L.; Luo, Yongkang; Thompson, J. D.; Bauer, E. D.

    2014-12-15

    The synthesis, crystal structure and physical properties studied by means of x-ray diffraction, magnetic, thermal and transport measurements of CeMAl4Si2 (M = Rh, Ir, Pt) are reported, along with the electronic structure calculations for LaMAl4Si2 (M = Rh, Ir, Pt). These materials adopt a tetragonal crystal structure (space group P4/mmm) comprised of BaAl4 blocks, separated by MAl2 units, stacked along the c-axis. Both CeRhAl4Si2 and CeIrAl4Si2 order antiferromagnetically below TN1 = 14 and 16 K, respectively, and undergo a second antiferromagnetic transitition at lower temperature (TN2 = 9 and 14 K, respectively). CePtAl4Si2 orders ferromagnetically below TC = 3 Kmore » with an ordered moment of μsat = 0.8 μB for a magnetic field applied perpendicular to the c-axis. Electronic structure calculations reveal quasi-2D character of the Fermi surface.« less

  19. The effect of Ce{sup 4+} incorporation on structural, morphological and photocatalytic characters of ZnO nanoparticles

    SciTech Connect (OSTI)

    Kannadasan, N.; Shanmugam, N. Cholan, S.; Sathishkumar, K.; Viruthagiri, G.; Poonguzhali, R.

    2014-11-15

    We report a simple chemical precipitation method for the preparation of undoped and cerium doped ZnO nanocrystals. The concentration of cerium in the products can be controlled in the range of 0.0250.125 mol. The structure and chemical compositions of the products were characterized by X-ray diffraction, X-ray photoelectron spectroscopy; energy dispersive spectrum and Fourier transform infrared spectroscopy. The results demonstrate that Ce{sup 4+} ions were successfully incorporated into the lattice position of Zn{sup 2+} ions in ZnO. The morphology of the products was analyzed by field emission scanning electron microscopy and confirmed by high resolution transmission electron microscope analysis. The optical properties of the products were studied by ultravioletvisible and room temperature photoluminescence measurements. The photoluminescence emission spectra of Ce-doped ZnO showed enhanced visible emissions as a result of 5d ? 4f transition of cerium. In particular, a novel photocatalytic activity of the products was assessed using methylene blue. The obtained result reveals that Ce-doped products show higher reduction efficiency for methylene blue than the undoped ZnO. - Highlights: Nanocrystals of ZnO and ZnO:Ce{sup 4+} were grown. XPS results confirmed the incorporated cerium in tetravalence. PL emission exhibited 5d ? 4f transition on cerium doping. Doped ZnO decolorizes MB faster than undoped ZnO.

  20. Superior performance of Ni-W-Ce mixed-metal oxide catalysts for ethanol steam reforming: Synergistic effects of W- and Ni-dopants

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Rodriguez, Jose A.; Liu, Zongyuan; Xu, Wenqian; Yao, Siyu; Johnson-Peck, Aaron C.; Zhao, Fuzhen; Michorczyk, Piotr; Kubacka, Anna; Stach, Eric A.; Fernandez-Garica, Marcos; et al

    2014-11-26

    The ethanol steam reforming (ESR) reaction was studied over a series of Ni-W-Ce oxide catalysts. The structures of the catalysts were characterized using in-situ techniques including X-ray diffraction, Pair Distribution Function, X-ray absorption fine structure and transmission electron microscopy; while possible surface intermediates for the ESR reaction were investigated by Diffuse Reflectance Infrared Fourier Transform Spectroscopy. In these materials, all the W and part of the Ni were incorporated into the CeO? lattice, with the remaining Ni forming highly dispersed nano NiO (moreThe Ni-W-Ce systeme exhibited a much larger lattice strain than those seen for Ni-Ce and W-Ce. Synergistic effects between Ni and W inside ceria produced a substantial amount of defects and O vacancies that led to high catalytic activity, selectivity and stability (i.e. resistance to coke formation) during ethanol steam reforming.less

  1. DOE - Office of Legacy Management -- Heavy Minerals Inc - IL 14

    Office of Legacy Management (LM)

    Heavy Minerals Inc - IL 14 FUSRAP Considered Sites Site: Heavy Minerals, Inc. ( IL.14 ) Eliminated from consideration under FUSRAP Designated Name: Not Designated Alternate Name: W.R. Grace Company IL.14-1 Location: 836 South Michigan Avenue , Chicago , Illinois IL.14-2 Evaluation Year: 1990 IL.14-1 Site Operations: Submitted a proposal to supply thorium hydroxide to the AEC; no indication that the bid was accepted. IL.14-2 Site Disposition: Eliminated - No indication of work done with

  2. Ionic liquid-assisted sonochemical preparation of CeO2 nanoparticles for CO oxidation

    SciTech Connect (OSTI)

    Alammar, Tarek; Noei, Heshmat; Wang, Yuemin; Grnert, Wolfgang; Mudring, Anja -Verena

    2014-10-10

    CeO2 nanoparticles were synthesized via a one-step ultrasound synthesis in different kinds of ionic liquids based on bis(trifluoromethanesulfonylamide, [Tf2N], in combination with various cations including 1-butyl-3-methylimidazolium ([C4mim]+), 1-ethyl-2,3-dimethylimidazolium ([Edimim]+), butyl-pyridinium([Py4]+), 1-butyl-1-methyl-pyrrolidinium ([Pyrr14]+), and 2-hydroxyethyl-trimethylammonium ([N1112OH]+). Depending on synthetic parameters, such as ionic liquid, Ce(IV) precursor, heating method, and precipitator, formed ceria exhibits different morphologies, varying from nanospheres, nanorods, nanoribbons, and nanoflowers. The morphology, crystallinity, and chemical composition of the obtained materials were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), energy dispersive X-ray spectroscopy (EDX), Raman spectroscopy, and N2 adsorption. The structural and electronic properties of the as-prepared CeO2 samples were probed by CO adsorption using IR spectroscopy under ultrahigh vacuum conditions. The catalytic activities of CeO2 nanoparticles were investigated in the oxidation of CO. CeO2 nanospheres obtained sonochemically in [C4mim][Tf2N] exhibit the best performance for low-temperature CO oxidation. As a result, the superior catalytic performance of this material can be related to its mesoporous structure, small particle size, large surface area, and high number of surface oxygen vacancy sites.

  3. Mineral density volume gradients in normal and diseased human tissues

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Djomehri, Sabra I.; Candell, Susan; Case, Thomas; Browning, Alyssa; Marshall, Grayson W.; Yun, Wenbing; Lau, S. H.; Webb, Samuel; Ho, Sunita P.; Aikawa, Elena

    2015-04-09

    Clinical computed tomography provides a single mineral density (MD) value for heterogeneous calcified tissues containing early and late stage pathologic formations. The novel aspect of this study is that, it extends current quantitative methods of mapping mineral density gradients to three dimensions, discretizes early and late mineralized stages, identifies elemental distribution in discretized volumes, and correlates measured MD with respective calcium (Ca) to phosphorus (P) and Ca to zinc (Zn) elemental ratios. To accomplish this, MD variations identified using polychromatic radiation from a high resolution micro-computed tomography (micro-CT) benchtop unit were correlated with elemental mapping obtained from a microprobe X-raymore » fluorescence (XRF) using synchrotron monochromatic radiation. Digital segmentation of tomograms from normal and diseased tissues (N=5 per group; 40-60 year old males) contained significant mineral density variations (enamel: 2820-3095mg/cc, bone: 570-1415mg/cc, cementum: 1240-1340mg/cc, dentin: 1480-1590mg/cc, cementum affected by periodontitis: 1100-1220mg/cc, hypomineralized carious dentin: 345-1450mg/cc, hypermineralized carious dentin: 1815-2740mg/cc, and dental calculus: 1290-1770mg/cc). A plausible linear correlation between segmented MD volumes and elemental ratios within these volumes was established, and Ca/P ratios for dentin (1.49), hypomineralized dentin (0.32-0.46), cementum (1.51), and bone (1.68) were observed. Furthermore, varying Ca/Zn ratios were distinguished in adapted compared to normal tissues, such as in bone (855-2765) and in cementum (595-990), highlighting Zn as an influential element in prompting observed adaptive properties. Hence, results provide insights on mineral density gradients with elemental concentrations and elemental footprints that in turn could aid in elucidating mechanistic processes for pathologic formations.« less

  4. Mineral density volume gradients in normal and diseased human tissues

    SciTech Connect (OSTI)

    Djomehri, Sabra I.; Candell, Susan; Case, Thomas; Browning, Alyssa; Marshall, Grayson W.; Yun, Wenbing; Lau, S. H.; Webb, Samuel; Ho, Sunita P.; Aikawa, Elena

    2015-04-09

    Clinical computed tomography provides a single mineral density (MD) value for heterogeneous calcified tissues containing early and late stage pathologic formations. The novel aspect of this study is that, it extends current quantitative methods of mapping mineral density gradients to three dimensions, discretizes early and late mineralized stages, identifies elemental distribution in discretized volumes, and correlates measured MD with respective calcium (Ca) to phosphorus (P) and Ca to zinc (Zn) elemental ratios. To accomplish this, MD variations identified using polychromatic radiation from a high resolution micro-computed tomography (micro-CT) benchtop unit were correlated with elemental mapping obtained from a microprobe X-ray fluorescence (XRF) using synchrotron monochromatic radiation. Digital segmentation of tomograms from normal and diseased tissues (N=5 per group; 40-60 year old males) contained significant mineral density variations (enamel: 2820-3095mg/cc, bone: 570-1415mg/cc, cementum: 1240-1340mg/cc, dentin: 1480-1590mg/cc, cementum affected by periodontitis: 1100-1220mg/cc, hypomineralized carious dentin: 345-1450mg/cc, hypermineralized carious dentin: 1815-2740mg/cc, and dental calculus: 1290-1770mg/cc). A plausible linear correlation between segmented MD volumes and elemental ratios within these volumes was established, and Ca/P ratios for dentin (1.49), hypomineralized dentin (0.32-0.46), cementum (1.51), and bone (1.68) were observed. Furthermore, varying Ca/Zn ratios were distinguished in adapted compared to normal tissues, such as in bone (855-2765) and in cementum (595-990), highlighting Zn as an influential element in prompting observed adaptive properties. Hence, results provide insights on mineral density gradients with elemental concentrations and elemental footprints that in turn could aid in elucidating mechanistic processes for pathologic formations.

  5. Fundamental study of CO2-H2O-mineral interactions for carbon sequestration,

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    with emphasis on the nature of the supercritical fluid-mineral interface. (Technical Report) | SciTech Connect Fundamental study of CO2-H2O-mineral interactions for carbon sequestration, with emphasis on the nature of the supercritical fluid-mineral interface. Citation Details In-Document Search Title: Fundamental study of CO2-H2O-mineral interactions for carbon sequestration, with emphasis on the nature of the supercritical fluid-mineral interface. In the supercritical CO2-water-mineral

  6. Magnetic hardening of Ce1+xFe11-yCoyTi with ThMn12 structure by melt

    Office of Scientific and Technical Information (OSTI)

    spinning (Journal Article) | SciTech Connect hardening of Ce1+xFe11-yCoyTi with ThMn12 structure by melt spinning Citation Details In-Document Search This content will become publicly available on April 15, 2016 Title: Magnetic hardening of Ce1+xFe11-yCoyTi with ThMn12 structure by melt spinning A recent study on the intrinsic magnetic properties of CeFe11-yCoyTi has revealed that substituting one Co for Fe retains the favorable magnetocrystalline anisotropy Ha found in the ternary Fe end

  7. Pressure-Induced Structural Phase Transition in CeNi: X-ray and Neutron Scattering Studies and First-Principles Calculations

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Mirmelstein, A.; Podlesnyak, Andrey A.; dos Santos, Antonio M.; Ehlers, Georg; Kerbel, O.; Matvienko, V.; Sefat, A. S.; Saporov, B.; Halder, G. J.; Tobin, J. G.

    2015-08-03

    The pressure-induced structural phase transition in the intermediate-valence compound CeNi has been investigated by x-ray and neutron powder diffraction techniques. It is shown that the structure of the pressure-induced CeNi phase (phases) can be described in terms of the Pnma space group. Equations of state for CeNi on both sides of the phase transition are derived and an approximate P-T phase diagram is suggested for Pmorethe phase transition.less

  8. Kondo hole behavior in Ce{sub 0.97} La{sub 0.03}Pd{sub 3}

    SciTech Connect (OSTI)

    Lawrence, J.M.; Graf, T.; Hundley, M.F.; Mandrus, D.; Thompson, J.D. [Los Alamos National Laboratory, Los Alamos, New Mexico 87545 (United States)] [Los Alamos National Laboratory, Los Alamos, New Mexico 87545 (United States); Lacerda, A.; Torikachvili, M.S. [National High Magnetic Field Laboratory, Pulse Facility, Los Alamos, New Mexico 87545 (United States)] [National High Magnetic Field Laboratory, Pulse Facility, Los Alamos, New Mexico 87545 (United States); Sarrao, J.L.; Fisk, Z. [National High Magnetic Field Laboratory, Florida State University, Tallahassee, Florida 32306 (United States)] [National High Magnetic Field Laboratory, Florida State University, Tallahassee, Florida 32306 (United States)

    1996-05-01

    We present results for the resistivity, the magnetoresistance, and the specific heat of Ce{sub 0.97}La{sub 0.03}Pd{sub 3} and CePd{sub 3}. The impurity contributions to these measurements follow the predictions of the single-impurity Kondo model for a Kondo temperature {ital T}{sub {ital L}}{approx_equal}65 K, assuming that the impurity behaves as a crystal-field split ({Gamma}{sub 7}) doublet. Assuming a {ital J}=5/2 impurity, the value of {ital T}{sub {ital L}} needed to fit these experiments varies from 65 to 125 K. The contribution to the susceptibility may be too small to be explained by the model. These results address whether the nonmagnetic impurity behaves as a Kondo hole. {copyright} {ital 1996 The American Physical Society.}

  9. Rend Lake College celebrates the opening of a new coal miner training facility

    SciTech Connect (OSTI)

    Buchsbaum, L.

    2009-09-15

    The Coal Miner Training Center at Rend Lake College recently hosted the Illinois Mining Institute's annual conference and a regional mine rescue competition. The article gives an outline of the coal miner training and refresher course offered. 3 photos.

  10. File:Land sale mineral release complete.pdf | Open Energy Information

    Open Energy Info (EERE)

    Land sale mineral release complete.pdf Jump to: navigation, search File File history File usage File:Land sale mineral release complete.pdf Size of this preview: 463 599 pixels....

  11. Geophysical technique for mineral exploration and discrimination based on electromagnetic methods and associated systems

    DOE Patents [OSTI]

    Zhdanov; Michael S.

    2008-01-29

    Mineral exploration needs a reliable method to distinguish between uneconomic mineral deposits and economic mineralization. A method and system includes a geophysical technique for subsurface material characterization, mineral exploration and mineral discrimination. The technique introduced in this invention detects induced polarization effects in electromagnetic data and uses remote geophysical observations to determine the parameters of an effective conductivity relaxation model using a composite analytical multi-phase model of the rock formations. The conductivity relaxation model and analytical model can be used to determine parameters related by analytical expressions to the physical characteristics of the microstructure of the rocks and minerals. These parameters are ultimately used for the discrimination of different components in underground formations, and in this way provide an ability to distinguish between uneconomic mineral deposits and zones of economic mineralization using geophysical remote sensing technology.

  12. RCW 79.14 Mineral, Coal, Oil and Gas Leases | Open Energy Information

    Open Energy Info (EERE)

    79.14 Mineral, Coal, Oil and Gas Leases Jump to: navigation, search OpenEI Reference LibraryAdd to library Legal Document- StatuteStatute: RCW 79.14 Mineral, Coal, Oil and Gas...

  13. Abiotic/Biotic Degradation and Mineralization of N-Nitrosodimethylamine in Aquifer Sediments

    SciTech Connect (OSTI)

    Szecsody, James E.; McKinley, James P.; Breshears, Andrew T.; Crocker, Fiona H.

    2008-10-14

    The N-nitrosodimethylamine (NDMA) degradation rate and mineralization rate were measured in two aquifer sediments that received treatments to create oxic, reducing, and sequential reducing/oxic environments. Chemically reduced sediments rapidly abiotically degraded NDMA to nontoxic dimethylamine (DMA) to parts per trillion levels, then degraded to further products. NDMA was partially mineralized in reduced sediments (6 to 28 percent) at a slow rate (half-life 3,460 h) by an unknown abiotic/biotic pathway. In contrast, NDMA was mineralized more rapidly (half-life 342 h) and to a greater extent (30 to 81 percent) in oxic sediments with propane addition, likely by a propane monooxygenase pathway. NDMA mineralization in sequential reduced sediment followed by oxic sediment treatment did result in slightly more rapid mineralization and a greater mineralization extent relative to reduced systems. These increases were minor, so aerobic NDMA mineralization with oxygen and propane addition was the most viable in situ NDMA mineralization strategy.

  14. File:03HIAReservedLandMineralLeasingProcess.pdf | Open Energy...

    Open Energy Info (EERE)

    HIAReservedLandMineralLeasingProcess.pdf Jump to: navigation, search File File history File usage Metadata File:03HIAReservedLandMineralLeasingProcess.pdf Size of this preview: 463...

  15. File:03HIBStateMineralLeasingProcess.pdf | Open Energy Information

    Open Energy Info (EERE)

    3HIBStateMineralLeasingProcess.pdf Jump to: navigation, search File File history File usage Metadata File:03HIBStateMineralLeasingProcess.pdf Size of this preview: 463 599...

  16. File:03AKAStateCompetitiveMineralLeasingProcess.pdf | Open Energy...

    Open Energy Info (EERE)

    3AKAStateCompetitiveMineralLeasingProcess.pdf Jump to: navigation, search File File history File usage Metadata File:03AKAStateCompetitiveMineralLeasingProcess.pdf Size of this...

  17. Strongly enhanced oxygen ion transport through samarium-doped CeO2 nanopillars in nanocomposite films

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Yang, Sang Mo; Lee, Shinbuhm; Jian, Jie; Zhang, Wenrui; Lu, Ping; Jia, Quanxi; Wang, Haiyan; Won Noh, Tae; Kalinin, Sergei V.; MacManus‐Driscoll, Judith L.

    2015-10-08

    Enhancement of oxygen ion conductivity in oxides is important for low-temperature (<500 °C) operation of solid oxide fuel cells, sensors and other ionotronic devices. While huge ion conductivity has been demonstrated in planar heterostructure films, there has been considerable debate over the origin of the conductivity enhancement, in part because of the difficulties of probing buried ion transport channels. Here we create a practical geometry for device miniaturization, consisting of highly crystalline micrometre-thick vertical nanocolumns of Sm-doped CeO2 embedded in supporting matrices of SrTiO3. The ionic conductivity is higher by one order of magnitude than plain Sm-doped CeO2films. Then bymore » using scanning probe microscopy, we show that the fast ion-conducting channels are not exclusively restricted to the interface but also are localized at the Sm-doped CeO2 nanopillars. Furthermore, this work offers a pathway to realize spatially localized fast ion transport in oxides of micrometre thickness.« less

  18. One-, two-, and three-channel Kondo effects for a model Ce{sup 3+} impurity in a metal

    SciTech Connect (OSTI)

    Kim, T.; Cox, D.L.

    1997-05-01

    We present studies of a simple Anderson model Hamiltonian for Ce{sup 3+} ions in cubic symmetry with three configurations (f{sup 0},f{sup 1},f{sup 2}). In different parameter regimes, our model Hamiltonian maps to the one-, two-, and three-channel spin-1/2 Kondo models. Using third-order scaling (perturbative renormalization group) analysis, we study the stability of the non-Fermi-liquid fixed point of the two-channel Kondo model for Ce{sup 3+} ions in cubic symmetry against the one-channel Kondo interaction. Using the noncrossing approximation (NCA), we also report detailed studies for our simplified model of the competition between the Fermi-liquid fixed point of the one-channel Kondo model and the non-Fermi fixed points of the two- and three-channel Kondo models. We provide the phase diagram in the model parameter space and study the thermodynamics and the transport properties of our simplified model Hamiltonian. Thermodynamics and transport coefficients show distinct behaviors for different numbers of channels. We confirm in detail that the NCA is a valid numerical method for the overcompensated multichannel S{sub I}=1/2 Anderson models. Our model study might be relevant to the non-Fermi-liquid alloy Ce{sub 1{minus}x}La{sub x}Cu{sub 2.2}Si{sub 2}. {copyright} {ital 1997} {ital The American Physical Society}

  19. Remarkably robust and correlated coherence and antiferromagnetism in (Ce1-xLax)Cu2Ge2

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Hodovanets, H.; Bud’ko, S. L.; Straszheim, W. E.; Taufour, V.; Mun, E. D.; Kim, H.; Flint, R.; Canfield, P. C.

    2015-06-08

    We present magnetic susceptibility, resistivity, specific heat, and thermoelectric power measurements on (Ce1-xLax)Cu2Ge2 single crystals (0 ≤ x ≤ 1). With La-substitution, the antiferromagnetic temperature TN is suppressed in an almost linear fashion and moves below 0.36 K, the base temperature of our measurements for x > 0.8. Surprisingly, in addition to robust antiferromagnetism, the system also shows low temperature coherent scattering below Tcoh up to ~0.9 of La, indicating a small percolation limit ~9% of Ce. Tcoh as a function of magnetic field was found to have different behavior for x < 0.9 and x > 0.9. Remarkably, (Tcoh)2more » at H = 0 was found to be linearly proportional to TN. In conclusion, the jump in the magnetic specific heat δCm at TN as a function of TK/TN for (Ce1-xLax)Cu2Ge2 follows the theoretical prediction based on the molecular field calculation for the S = 1/2 resonant level model.« less

  20. Strongly enhanced oxygen ion transport through samarium-doped CeO2 nanopillars in nanocomposite films

    SciTech Connect (OSTI)

    Yang, Sang Mo; Lee, Shinbuhm; Jian, Jie; Zhang, Wenrui; Lu, Ping; Jia, Quanxi; Wang, Haiyan; Won Noh, Tae; Kalinin, Sergei V.; MacManus?Driscoll, Judith L.

    2015-10-08

    Enhancement of oxygen ion conductivity in oxides is important for low-temperature (<500 C) operation of solid oxide fuel cells, sensors and other ionotronic devices. While huge ion conductivity has been demonstrated in planar heterostructure films, there has been considerable debate over the origin of the conductivity enhancement, in part because of the difficulties of probing buried ion transport channels. Here we create a practical geometry for device miniaturization, consisting of highly crystalline micrometre-thick vertical nanocolumns of Sm-doped CeO2 embedded in supporting matrices of SrTiO3. The ionic conductivity is higher by one order of magnitude than plain Sm-doped CeO2films. Then by using scanning probe microscopy, we show that the fast ion-conducting channels are not exclusively restricted to the interface but also are localized at the Sm-doped CeO2 nanopillars. Furthermore, this work offers a pathway to realize spatially localized fast ion transport in oxides of micrometre thickness.

  1. Strongly enhanced oxygen ion transport through samarium-doped CeO2 nanopillars in nanocomposite films

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Yang, Sangmo; Lee, Shinbuhm; Jian, Jie; Zhang, Wenrui; Lu, Ping; Jia, Quanxi; Wang, Haiyan; Noh, Tae Won; Kalinin, Sergei V.; MacManus-Driscoll, Judith L.

    2015-10-08

    Enhancement of oxygen ion conductivity in oxides is important for low-temperature (<500 °C) operation of solid oxide fuel cells, sensors and other ionotronic devices. While huge ion conductivity has been demonstrated in planar heterostructure films, there has been considerable debate over the origin of the conductivity enhancement, in part because of the difficulties of probing buried ion transport channels. Here we create a practical geometry for device miniaturization, consisting of highly crystalline micrometre-thick vertical nanocolumns of Sm-doped CeO2 embedded in supporting matrices of SrTiO3. The ionic conductivity is higher by one order of magnitude than plain Sm-doped CeO2 films. Bymore » using scanning probe microscopy, we show that the fast ion-conducting channels are not exclusively restricted to the interface but also are localized at the Sm-doped CeO2 nanopillars. This work offers a pathway to realize spatially localized fast ion transport in oxides of micrometre thickness.« less

  2. Effect of Oxygen Defects on the Catalytic Performance of VOx/CeO2 Catalysts for Oxidative Dehydrogenation of Methanol

    SciTech Connect (OSTI)

    Li, Yan; Wei, Zhehao; Gao, Feng; Kovarik, Libor; Baylon, Rebecca A.; Peden, Charles HF; Wang, Yong

    2015-05-01

    In this work, CeO2 nanocubes with controlled particle size and dominating (100) facets are synthesized as supports for VOx catalysts. Combined TEM, SEM, XRD, and Raman study reveals that the oxygen vacancy density of CeO2 supports can be tuned by tailoring the particle sizes without altering the dominating facets, where smaller particle sizes result in larger oxygen vacancy densities. At the same vanadium coverage, the VOx catalysts supported on small-sized CeO2 supports with higher oxygen defect densities exhibit promoted redox property and lower activation energy for methoxyl group decomposition, as evidenced by H2-TPR and methanol TPD study. These results further confirm that the presence of oxygen vacancies plays an important role in promoting the activity of VOx species in methanol oxidation. We gratefully acknowledge financial support from the U.S. Department of Energy (DOE), Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences, and Biosciences. Part of this work was conducted in the William R. Wiley Environmental Molecular Sciences Laboratory (EMSL), a national scientific user facility sponsored by DOE’s Office of Biological and Environmental Research and located at Pacific Northwest National Laboratory (PNNL). PNNL is a multiprogram national laboratory operated for the DOE by Battelle.

  3. Radiolysis of alanine adsorbed in a clay mineral

    SciTech Connect (OSTI)

    Aguilar-Ovando, Ellen Y.; Negron-Mendoza, Alicia

    2013-07-03

    Optical activity in molecules is a chemical characteristic of living beings. In this work, we examine the hypothesis of the influence of different mineral surfaces on the development of a specific chirality in organic molecules when subjected to conditions simulating the primitive Earth during the period of chemical evolution. By using X-ray diffraction techniques and HPLC/ELSD to analyze aqueous suspensions of amino acids adsorbed on minerals irradiated in different doses with a cobalt-60 gamma source, the experiments attempt to prove the hypothesis that some solid surfaces (like clays and meteorite rocks) may have a concentration capacity and protective role against external sources of ionizing radiation (specifically {gamma}-ray) for some organic compounds (like some amino acids) adsorbed on them. Preliminary results show a slight difference in the adsorption and radiolysis of the D-and L-alanine.

  4. Investigating Radiation Shielding Properties of Different Mineral Origin Heavyweight Concretes

    SciTech Connect (OSTI)

    Basyigit, Celalettin; Uysal, Volkan; Kilincarslan, Semsettin; Akkas, Ayse; Mavi, Betuel; Guenoglu, Kadir; Akkurt, Iskender

    2011-12-26

    The radiation although has hazardous effects for human health, developing technologies bring lots of usage fields to radiation like in medicine and nuclear power station buildings. In this case protecting from undesirable radiation is a necessity for human health. Heavyweight concrete is one of the most important materials used in where radiation should be shielded, like those areas. In this study, used heavyweight aggregates of different mineral origin (Limonite, Siderite), in order to prepare different series in concrete mixtures and investigated radiation shielding properties. The experimental results on measuring the radiation shielding, the heavyweight concrete prepared with heavyweight aggregates of different mineral origin show that, are useful radiation absorbents when they used in concrete mixtures.

  5. Method of analysis of asbestiform minerals by thermoluminescence

    DOE Patents [OSTI]

    Fisher, Gerald L. (Davis, CA); Bradley, Edward W. (Davis, CA)

    1980-01-01

    A method for the qualitative and quantitative analysis of asbestiform minerals, including the steps of subjecting a sample to be analyzed to the thermoluminescent analysis, annealing the sample, subjecting the sample to ionizing radiation, and subjecting the sample to a second thermoluminescent analysis. Glow curves are derived from the two thermoluminescent analyses and their shapes then compared to established glow curves of known asbestiform minerals to identify the type of asbestiform in the sample. Also, during at least one of the analyses, the thermoluminescent response for each sample is integrated during a linear heating period of the analysis in order to derive the total thermoluminescence per milligram of sample. This total is a measure of the quantity of asbestiform in the sample and may also be used to identify the source of the sample.

  6. An active atmospheric methane sink in high Arctic mineral cryosols

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Lau, Maggie C.Y.; Stackhouse, B.; Layton, Alice C.; Chauhan, Archana; Vishnivetskaya, T. A.; Chourey, Karuna; Mykytczuk, N. C.S.; Bennett, Phil C.; Lamarche-Gagnon, G.; Burton, N.; et al

    2015-04-14

    The transition of Arctic carbon-rich cryosols into methane (CH₄)-emitting wetlands due to global warming is a rising concern. However, the spatially predominant mineral cryosols and their CH₄ emission potential are poorly understood. Fluxes measured in situ and estimated under laboratory conditions coupled with -omics analysis indicate (1) mineral cryosols in the Canadian high Arctic contain atmospheric CH₄-oxidizing bacteria; (2) the atmospheric CH⁺ uptake flux increases with ground temperature; and, as a result, (3) the atmospheric CH₄ sink strength will increase by a factor of 5-30 as the Arctic warms by 5-15 °C over a century. We demonstrated that acidic mineralmore » cryosols have previously unrecognized potential of negative CH₄ feedback.« less

  7. Hydrodesulfurization and hydrodenitrogenation catalysts obtained from coal mineral matter

    DOE Patents [OSTI]

    Liu, Kindtoken H. D. (Newark, DE); Hamrin, Jr., Charles E. (Lexington, KY)

    1982-01-01

    A hydrotreating catalyst is prepared from coal mineral matter obtained by low temperature ashing coals of relatively low bassanite content by the steps of: (a) depositing on the low temperature ash 0.25-3 grams of an iron or nickel salt in water per gram of ash and drying a resulting slurry; (b) crushing and sizing a resulting solid; and (c) heating the thus-sized solid powder in hydrogen.

  8. Mineral Deformation at Earth's Core-Mantle Boundary

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Mineral Deformation at Earth's Core-Mantle Boundary Print Earth is a dynamic planet in which convection takes place on the scale of thousands of kilometers. Because Earth is mostly solid (except for its liquid-iron outer core), this convection causes deformation of solid rocks by plastic flow. At the core-mantle boundary (CMB), 2900 km deep, seismologists have discovered that seismic waves travel faster in certain directions. This seismic anisotropy appears to be related to the deformation of

  9. Mineral Deformation at Earth's Core-Mantle Boundary

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Mineral Deformation at Earth's Core-Mantle Boundary Print Earth is a dynamic planet in which convection takes place on the scale of thousands of kilometers. Because Earth is mostly solid (except for its liquid-iron outer core), this convection causes deformation of solid rocks by plastic flow. At the core-mantle boundary (CMB), 2900 km deep, seismologists have discovered that seismic waves travel faster in certain directions. This seismic anisotropy appears to be related to the deformation of

  10. Mineral Deformation at Earth's Core-Mantle Boundary

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Mineral Deformation at Earth's Core-Mantle Boundary Print Earth is a dynamic planet in which convection takes place on the scale of thousands of kilometers. Because Earth is mostly solid (except for its liquid-iron outer core), this convection causes deformation of solid rocks by plastic flow. At the core-mantle boundary (CMB), 2900 km deep, seismologists have discovered that seismic waves travel faster in certain directions. This seismic anisotropy appears to be related to the deformation of

  11. Dissolving the mineral calcite: Reaction front instability | Argonne

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    National Laboratory calcite: Reaction front instability Share Topic Programs Chemical sciences & engineering Synchrotron radiation X-ray imaging & holography Using the X-ray Reflection Interfacial Microscope powered by the Advanced Photon Source, researchers can both watch and drive the nanoscale changes of the surface of a calcite mineral as it dissolves in real-time. In this image, researchers observe distortions in the reaction front (the boundary between the blue and red regions)

  12. Mineral Deformation at Earth's Core-Mantle Boundary

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Mineral Deformation at Earth's Core-Mantle Boundary Print Earth is a dynamic planet in which convection takes place on the scale of thousands of kilometers. Because Earth is mostly solid (except for its liquid-iron outer core), this convection causes deformation of solid rocks by plastic flow. At the core-mantle boundary (CMB), 2900 km deep, seismologists have discovered that seismic waves travel faster in certain directions. This seismic anisotropy appears to be related to the deformation of

  13. Mineral Deformation at Earth's Core-Mantle Boundary

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Mineral Deformation at Earth's Core-Mantle Boundary Print Earth is a dynamic planet in which convection takes place on the scale of thousands of kilometers. Because Earth is mostly solid (except for its liquid-iron outer core), this convection causes deformation of solid rocks by plastic flow. At the core-mantle boundary (CMB), 2900 km deep, seismologists have discovered that seismic waves travel faster in certain directions. This seismic anisotropy appears to be related to the deformation of

  14. Mineral Deformation at Earth's Core-Mantle Boundary

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Mineral Deformation at Earth's Core-Mantle Boundary Print Earth is a dynamic planet in which convection takes place on the scale of thousands of kilometers. Because Earth is mostly solid (except for its liquid-iron outer core), this convection causes deformation of solid rocks by plastic flow. At the core-mantle boundary (CMB), 2900 km deep, seismologists have discovered that seismic waves travel faster in certain directions. This seismic anisotropy appears to be related to the deformation of

  15. Mineral Deformation at Earth's Core-Mantle Boundary

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Mineral Deformation at Earth's Core-Mantle Boundary Print Earth is a dynamic planet in which convection takes place on the scale of thousands of kilometers. Because Earth is mostly solid (except for its liquid-iron outer core), this convection causes deformation of solid rocks by plastic flow. At the core-mantle boundary (CMB), 2900 km deep, seismologists have discovered that seismic waves travel faster in certain directions. This seismic anisotropy appears to be related to the deformation of

  16. Mineral Deformation at Earth's Core-Mantle Boundary

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Mineral Deformation at Earth's Core-Mantle Boundary Print Earth is a dynamic planet in which convection takes place on the scale of thousands of kilometers. Because Earth is mostly solid (except for its liquid-iron outer core), this convection causes deformation of solid rocks by plastic flow. At the core-mantle boundary (CMB), 2900 km deep, seismologists have discovered that seismic waves travel faster in certain directions. This seismic anisotropy appears to be related to the deformation of

  17. DOE - Office of Legacy Management -- International Minerals and Chemical

    Office of Legacy Management (LM)

    Corp - Pilot Plant - FL 02 and Chemical Corp - Pilot Plant - FL 02 FUSRAP Considered Sites Site: International Minerals and Chemical Corp - Pilot Plant (FL.02) Designated Name: Not Designated Alternate Name: None Location: Mulberry , Florida FL.02-1 Evaluation Year: 1985 FL.02-2 Site Operations: Erected and operated a pilot plant to process material from the leached zone of the Florida pebble phosphate field for the recovery of uranium and other saleable products and also conducted

  18. DOE - Office of Legacy Management -- International Minerals and Chemicals

    Office of Legacy Management (LM)

    Corp - Bonnie Mill Plant - FL 03 and Chemicals Corp - Bonnie Mill Plant - FL 03 FUSRAP Considered Sites Site: International Minerals and Chemicals Corp., Bonnie Mill Plant (FL.03) Eliminated from consideration under FUSRAP Designated Name: Not Designated Alternate Name: CF Industries Bonnie Uranium Plant FL.03-2 Location: Approximately 2 miles south of Highway 60 between Mulberry and Bartow , Bartow , Florida FL.03-2 Evaluation Year: 1985 FL.03-2 Site Operations: Recovered uranium

  19. Division of Energy and Mineral Development - Project Overviews

    Office of Environmental Management (EM)

    Secretary-Indian Affairs Office of Indian Energy and Economic Development Project Overviews Scott Haase Renewable Energy Engineer ASIA, Division of Energy and Mineral Development Presented at: U.S. DOE Tribal Energy Program Annual Meeting October 26, 2006 Prior to April 14, 2005 the Division was under the Office of Trust Services. The Division now reports to a newly formed office - The Office of Indian Energy and Economic Development Bureau of Indian Affairs Secretary, Policy and Economic

  20. Methanol conversion to light olefins over nanostructured CeAPSO-34 catalyst: Thermodynamic analysis of overall reactions and effect of template type on catalytic properties and performance

    SciTech Connect (OSTI)

    Aghamohammadi, Sogand; Haghighi, Mohammad; Charghand, Mojtaba

    2014-02-01

    Graphical abstract: In this research nanostructured CeAPSO-34 was synthesized to explore the effect of TEAOH and morpholine on its physiochemical properties and MTO performance. Prepared catalysts were characterized with XRD, FESEM, BET, FTIR and NH3-TPD techniques. The results indicated that the nature of the template determines the physiochemical properties of CeAPSO-34 due to different rate of crystal growth. The catalyst obtained by using morpholine showed longer life time as well as sustaining light olefins selectivity at higher values. Furthermore, a comprehensive thermodynamic analysis of overall reactions network was carried out to address the major channels of methanol to olefins conversion. - Highlights: Introduction of Ce into SAPO-34 framework. Comparison of CeAPSO-34 synthesized using morpholine and TEAOH. The nature of the template determines the physiochemical properties of CeAPSO-34. Morpholine enhances catalyst lifetime in MTO process. Presenting a complete reaction network for MTO process. - Abstract: TEAOH and morpholine were employed in synthesis of nanostructured CeAPSO-34 molecular sieve and used in methanol to olefins conversion. Prepared samples were characterized by XRD, FESEM, EDX, BET, FTIR and NH{sub 3}-TPD techniques. XRD patterns reflected the higher crystallinity of the catalyst synthesized with morpholine. The FESEM results indicated that the nature of the template determines the morphology of nanostructured CeAPSO-34 due to different rate of crystal growth. There was a meaningful difference in the strength of both strong and weak acid sites for CeAPSO-34 catalysts synthesized with TEAOH and morpholine templates. The catalyst synthesized with morpholine showed higher desorption temperature of both weak and strong acid sites evidenced by NH{sub 3}-TPD characterization. The catalyst obtained using morpholine template had the longer lifetime and sustained desired light olefins at higher values. A comprehensive thermodynamic analysis of overall reactions network was carried out to address the major channels of methanol to olefins conversion.

  1. SESAME 96170, a solid-liquid equation of state for CeO2

    SciTech Connect (OSTI)

    Chisolm, Eric D.

    2014-05-02

    I describe an equation of state (EOS) for the low-pressure solid phase and liquid phase of cerium (IV) oxide, CeO2. The models and parameters used to calculate the EOS are presented in detail, and I compare with data for the full-density crystal. Hugoniot data are available only for high-porosity powders, and I discuss difficulties in comparing with such data. I have constructed SESAME 96170, an EOS for cerium (IV) oxide that includes the ambient solid and liquid phases. The EOS extends over the full standard SESAME range, but should not be used at low temperatures and high densities because of the lack of a high-pressure solid phase. I have described the models used to compute the three terms of the EOS (cold curve, nuclear, and thermal electronic), and I have given the parameters used in the models. They were determined by comparison with experimental data at P = 1 atm, including the constant-pressure specific heat, coefficient of thermal expansion, and melting and boiling points. The EOS compares well with data in its intended range of validity, but the presence of high-frequency optical modes in its phonon spectrum limits the agreement of our models with thermal data. The next step is to construct a multiphase EOS that includes the low- and high-pressure solid phases and the liquid. The DAC data from Duclos will most strongly constrain the parameters of the high-pressure solid. A remaining issue is the comparison of the crystal-density EOS with experimental Hugoniot data, which are taken at much lower initial data because the samples are porous powders. A satisfactory means of modeling porosity, allowing comparison of theory and experiment, has not yet been produced.

  2. A ferromagnetic quantum critical point in heavy-fermion iron oxypnictide CeFe{sub 1?x}Cr{sub x}PO

    SciTech Connect (OSTI)

    Okano, T.; Matoba, M.; Kamihara, Y.; Kitao, S.; Seto, M.; Atou, T.; Itoh, M.

    2015-05-07

    We report crystallographic and magnetic properties of layered iron oxypnictide CeFe{sub 1?x}Cr{sub x}PO (x?=?0.0000.692). Interlayer distances between Ce{sub 2}O{sub 2} and (Fe{sub 1?x}Cr{sub x}){sub 2}P{sub 2} layers increase as a function of x, suggesting suppression of Kondo coupling among hybridized conducting orbitals and localized Ce 4f orbitals. CeFe{sub 1?x}Cr{sub x}PO (x?=?0.1000.384) exhibits finite ferromagnetic transition temperatures (T{sub curie}) obtained by Arrott plots, although {sup 57}Fe Mssbauer spectra reveal paramagnetic Fe sublattice at T???4.2?K. These results indicate that the ferromagnetic phase transitions of samples are mainly due to Ce sublattice. For the samples with x???0.500, no ferromagnetic order is observed down to 2?K. These results verify that ferromagnetic quantum critical points of CeFe{sub 1?x}Cr{sub x}PO appear at 0.045???x???0.100 and 0.384???x???0.500.

  3. Superior performance of Ni-W-Ce mixed-metal oxide catalysts for ethanol steam reforming: Synergistic effects of W- and Ni-dopants

    SciTech Connect (OSTI)

    Rodriguez, Jose A.; Liu, Zongyuan; Xu, Wenqian; Yao, Siyu; Johnson-Peck, Aaron C.; Zhao, Fuzhen; Michorczyk, Piotr; Kubacka, Anna; Stach, Eric A.; Fernandez-Garica, Marcos; Senanayake, Sanjaya D.

    2014-11-26

    The ethanol steam reforming (ESR) reaction was studied over a series of Ni-W-Ce oxide catalysts. The structures of the catalysts were characterized using in-situ techniques including X-ray diffraction, Pair Distribution Function, X-ray absorption fine structure and transmission electron microscopy; while possible surface intermediates for the ESR reaction were investigated by Diffuse Reflectance Infrared Fourier Transform Spectroscopy. In these materials, all the W and part of the Ni were incorporated into the CeO? lattice, with the remaining Ni forming highly dispersed nano NiO (< 2 nm) outside the Ni-W-Ce oxide structure. The nano NiO was reduced to Ni under ESR conditions. The Ni-W-Ce systeme exhibited a much larger lattice strain than those seen for Ni-Ce and W-Ce. Synergistic effects between Ni and W inside ceria produced a substantial amount of defects and O vacancies that led to high catalytic activity, selectivity and stability (i.e. resistance to coke formation) during ethanol steam reforming.

  4. Crystalline Electric Field as a Probe for Long-Range Antiferromagnetic Order and Superconducting State of CeFeAsO1-xFx

    SciTech Connect (OSTI)

    Chi, Songxue; Adroja, D. T.; GUIDI, T.; Bewley, Robert I.; Li, Shiliang; Zhao, Jun; Lynn, J. W.; Brown, C. M.; Qiu, Y.; Chen, G. F,; Luo, J. L.; Wang, N. L.; Dai, Pengcheng

    2008-01-01

    We use inelastic neutron scattering to study the crystalline electric field (CEF) excitations of Ce{sup 3+} in CeFeAsO{sub 1-x}F{sub x} (x=0, 0.16). For nonsuperconducting CeFeAsO, the Ce CEF levels have three magnetic doublets in the paramagnetic state, but these doublets split into six singlets when the Fe ions order antiferromagnetically. For superconducting CeFeAsO{sub 0.84}F{sub 0.16} (T{sub c} = 41 K), where the static antiferromagnetic order is suppressed, the Ce CEF levels have three magnetic doublets at {h_bar}{sub {omega}} = 0, 18.7, 58.4 meV at all temperatures. Careful measurements of the intrinsic linewidth {Lambda} and the peak position of the 18.7 meV mode reveal a clear anomaly at T{sub c}, consistent with a strong enhancement of local magnetic susceptibility {chi}{double_prime}({h_bar}{sub {omega}}) below T{sub c}. These results suggest that CEF excitations in the rare-earth oxypnictides can be used as a probe of spin dynamics in the nearby FeAs planes.

  5. Superior performance of NiWCe mixed-metal oxide catalysts for ethanol steam reforming: Synergistic effects of W- and Ni-dopants

    SciTech Connect (OSTI)

    Liu, Zongyuan; Xu, Wenqian; Yao, Siyu; Johnson-Peck, Aaron C.; Zhao, Fuzhen; Michorczyk, Piotr; Kubacka, Anna; Stach, Eric A.; Fernndez-Garca, Marcos; Senanayake, Sanjaya D.; Rodriguez, Jos A.

    2014-11-26

    In this study, the ethanol steam reforming (ESR) reaction was examined over a series of Ni-W-Ce oxide catalysts. The structures of the catalysts were characterized using in-situ techniques including X-ray diffraction, Pair Distribution Function, X-ray absorption fine structure and transmission electron microscopy; while possible surface intermediates for the ESR reaction were investigated by Diffuse Reflectance Infrared Fourier Transform Spectroscopy. In these materials, all the W and part of the Ni were incorporated into the CeO? lattice, with the remaining Ni forming highly dispersed nano NiO (< 2 nm) outside the Ni-W-Ce oxide structure. The nano NiO was reduced to Ni under ESR conditions. The Ni-W-Ce systeme exhibited a much larger lattice strain than those seen for Ni-Ce and W-Ce. Synergistic effects between Ni and W inside ceria produced a substantial amount of defects and O vacancies that led to high catalytic activity, selectivity and stability (i.e. resistance to coke formation) during ethanol steam reforming.

  6. Superior performance of Ni–W–Ce mixed-metal oxide catalysts for ethanol steam reforming: Synergistic effects of W- and Ni-dopants

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Liu, Zongyuan; Xu, Wenqian; Yao, Siyu; Johnson-Peck, Aaron C.; Zhao, Fuzhen; Michorczyk, Piotr; Kubacka, Anna; Stach, Eric A.; Fernández-García, Marcos; Senanayake, Sanjaya D.; et al

    2014-11-26

    In this study, the ethanol steam reforming (ESR) reaction was examined over a series of Ni-W-Ce oxide catalysts. The structures of the catalysts were characterized using in-situ techniques including X-ray diffraction, Pair Distribution Function, X-ray absorption fine structure and transmission electron microscopy; while possible surface intermediates for the ESR reaction were investigated by Diffuse Reflectance Infrared Fourier Transform Spectroscopy. In these materials, all the W and part of the Ni were incorporated into the CeO₂ lattice, with the remaining Ni forming highly dispersed nano NiO (< 2 nm) outside the Ni-W-Ce oxide structure. The nano NiO was reduced to Nimore » under ESR conditions. The Ni-W-Ce systeme exhibited a much larger lattice strain than those seen for Ni-Ce and W-Ce. Synergistic effects between Ni and W inside ceria produced a substantial amount of defects and O vacancies that led to high catalytic activity, selectivity and stability (i.e. resistance to coke formation) during ethanol steam reforming.« less

  7. Fundamental study of CO2-H2O-mineral interactions for carbon sequestration,

    Office of Scientific and Technical Information (OSTI)

    with emphasis on the nature of the supercritical fluid-mineral interface. (Technical Report) | SciTech Connect Technical Report: Fundamental study of CO2-H2O-mineral interactions for carbon sequestration, with emphasis on the nature of the supercritical fluid-mineral interface. Citation Details In-Document Search Title: Fundamental study of CO2-H2O-mineral interactions for carbon sequestration, with emphasis on the nature of the supercritical fluid-mineral interface. In the supercritical

  8. Fundamental study of CO2-H2O-mineral interactions for carbon sequestration,

    Office of Scientific and Technical Information (OSTI)

    with emphasis on the nature of the supercritical fluid-mineral interface. (Technical Report) | SciTech Connect Fundamental study of CO2-H2O-mineral interactions for carbon sequestration, with emphasis on the nature of the supercritical fluid-mineral interface. Citation Details In-Document Search Title: Fundamental study of CO2-H2O-mineral interactions for carbon sequestration, with emphasis on the nature of the supercritical fluid-mineral interface. × You are accessing a document from the

  9. Ba{sub 2}B{sub 2}O{sub 5}:Ce{sup 3+}: A novel blue emitting phosphor for white LEDs

    SciTech Connect (OSTI)

    Li, Panlai Wang, Zhijun Yang, Zhiping; Guo, Qinglin

    2014-12-15

    Graphical abstract: Under the 350 nm radiation excitation, Ba{sub 2}B{sub 2}O{sub 5}:Ce{sup 3+} has a broad blue emission band. When the temperature turned up to 150 C, the emission intensity of Ba{sub 1.97}B{sub 2}O{sub 5}:0.03Ce{sup 3+} is 63.4% of the initial value at room temperature. The activation energy ?E is calculated to be 0.25 eV, which prove the good thermal stability of Ba{sub 2}B{sub 2}O{sub 5}:Ce{sup 3+}. All the properties indicate that Ba{sub 2}B{sub 2}O{sub 5}:Ce{sup 3+} may have potential application in white LEDs. - Highlights: Ba{sub 2}B{sub 2}O{sub 5}:Ce{sup 3+} has a broad blue emission band under the 350 nm radiation excitation. Emission intensity of Ba{sub 2}B{sub 2}O{sub 5}:Ce{sup 3+} is 63.4% (150 C) of the initial value (30 C). The activation energy ?E for thermal quenching is 0.25 eV. - Abstract: A novel blue emitting phosphor Ba{sub 2}B{sub 2}O{sub 5}:Ce{sup 3+} is synthesized by a high temperature solid state method. The luminescent property and the thermal stability of Ba{sub 2}B{sub 2}O{sub 5}:Ce{sup 3+} are investigated. Under the 350 nm radiation excitation, Ba{sub 2}B{sub 2}O{sub 5}:Ce{sup 3+} has a broad blue emission band, and the peak locates at 417 nm which is assigned to the 5d{sup 1}4f{sup 1} transition of Ce{sup 3+}. It is further proved that the dipoledipole interaction results in the concentration quenching of Ce{sup 3+} in Ba{sub 2}B{sub 2}O{sub 5}:Ce{sup 3+}. When the temperature turned up to 150 C, the emission intensity of Ba{sub 1.97}B{sub 2}O{sub 5}:0.03Ce{sup 3+} is 63.4% of the initial value at room temperature. The activation energy ?E is calculated to be 0.25 eV, which prove the good thermal stability of Ba{sub 2}B{sub 2}O{sub 5}:Ce{sup 3+}. All the properties indicate that Ba{sub 2}B{sub 2}O{sub 5}:Ce{sup 3+} may have potential application in white LEDs.

  10. Hierarchical Heterogeneity at the CeO x –TiO 2 Interface: Electronic and Geometric Structural Influence on the Photocatalytic Activity of Oxide on Oxide Nanostructures

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Luo, Si; Nguyen-Phan, Thuy-Duong; Johnston-Peck, Aaron C.; Barrio, Laura; Sallis, Shawn; Arena, Dario A.; Kundu, Shankhamala; Xu, Wenqian; Piper, Louis F. J.; Stach, Eric A.; et al

    2015-01-13

    Mixed oxide interfaces are critical for delivering active components of demanding catalytic processes such as the photo-catalytic splitting of water. We have studied CeOxTiO₂ catalysts with low ceria loadings of 1 wt%, 3 wt% and 6 wt% that were prepared with wet impregnation methods to favor a strong interaction between CeOx and TiO₂. In these materials the interfaces between CeOx-TiO₂ have been sequentially loaded (1%, 3% and 6%), with and without Pt (0.5 wt%). The structure and properties of the catalysts were characterized using several X-ray and electron based techniques including XRD, XPS, UPS, NEXAFS, UV-Vis and HR-STEM/STEM-EELS, to unravelmore » the local morphology, bulk structure, surface states and electronic structure. The combination of all these techniques allow us to analyze in a systematic way the complete structural and electronic properties that prevail at the CeOx-TiO₂ interface. Fluorite structured nano crystallites of ceria on anatase-structured titania were identified by both XRD and NEXAFS. A sequential increasing of the CeOx loading led to the formation of clusters, then plates and finally nano particles in a hierarchical manner on the TiO₂ support. The electronic structures of these catalysts indicate that the interaction between TiO₂ and CeO₂ is closely related to the local morphology of nanostructured CeO₂. Ce³⁺ cations were detected at the surface of CeO₂ and at the interface of the two oxides. In addition, the titania is perturbed by the interaction with ceria and also with Pt. The photocatalytic activity for the splitting of H₂O using UV light was measured for these materials and correlated with our understanding of the electronic and structural properties. Optimal catalytic performance and photo response results were found for the 1 wt% CeOx-TiO₂ catalyst where low dimensional geometry of the ceria provided ideal electronic and geometrical properties. The structural and electronic properties of the interface were critical for the photocatalytic performance of this mixed-oxide nanocatalyst system.« less

  11. Hierarchical heterogeneity at the CeOx-TiO? interface: Electronic and geometric structural influence on the photocatalytic activity of oxide on oxide nanostructures

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    None

    2015-01-13

    Mixed oxide interfaces are critical for delivering active components of demanding catalytic processes such as the photo-catalytic splitting of water. We have studied CeOxTiO? catalysts with low ceria loadings of 1 wt%, 3 wt% and 6 wt% that were prepared with wet impregnation methods to favor a strong interaction between CeOx and TiO?. In these materials the interfaces between CeOx-TiO? have been sequentially loaded (1%, 3% and 6%), with and without Pt (0.5 wt%). The structure and properties of the catalysts were characterized using several X-ray and electron based techniques including XRD, XPS, UPS, NEXAFS, UV-Vis and HR-STEM/STEM-EELS, to unravelmorethe local morphology, bulk structure, surface states and electronic structure. The combination of all these techniques allow us to analyze in a systematic way the complete structural and electronic properties that prevail at the CeOx-TiO? interface. Fluorite structured nano crystallites of ceria on anatase-structured titania were identified by both XRD and NEXAFS. A sequential increasing of the CeOx loading led to the formation of clusters, then plates and finally nano particles in a hierarchical manner on the TiO? support. The electronic structures of these catalysts indicate that the interaction between TiO? and CeO? is closely related to the local morphology of nanostructured CeO?. Ce? cations were detected at the surface of CeO? and at the interface of the two oxides. In addition, the titania is perturbed by the interaction with ceria and also with Pt. The photocatalytic activity for the splitting of H?O using UV light was measured for these materials and correlated with our understanding of the electronic and structural properties. Optimal catalytic performance and photo response results were found for the 1 wt% CeOx-TiO? catalyst where low dimensional geometry of the ceria provided ideal electronic and geometrical properties. The structural and electronic properties of the interface were critical for the photocatalytic performance of this mixed-oxide nanocatalyst system.less

  12. NOVEL IN-SITU METAL AND MINERAL EXTRACTION TECHNOLOGY

    SciTech Connect (OSTI)

    Glenn O'Gorman; Hans von Michaelis; Gregory J. Olson

    2004-09-22

    This white paper summarizes the state of art of in-situ leaching of metals and minerals, and describes a new technology concept employing improved fragmentation of ores underground in order to prepare the ore for more efficient in-situ leaching, combined with technology to continuously improve solution flow patterns through the ore during the leaching process. The process parameters and economic benefits of combining the new concept with chemical and biological leaching are described. A summary is provided of the next steps required to demonstrate the technology with the goal of enabling more widespread use of in-situ leaching.

  13. Rare earth element patterns in biotite, muscovite and tourmaline minerals

    SciTech Connect (OSTI)

    Laul, J.C.; Lepel, E.A.

    1986-04-21

    Rare earth element concentrations in the minerals biotite and muscovite from the mica schist country rocks of the Etta pegmatite and tourmalines from the Bob Ingersoll pegmatite have been measured by INAA and CNAA. The concentrations range from 10/sup -4/ g/g to 10/sup -10g//sub g/. The REE patterns of biotite, muscovite and tourmaline reported herein are highly fractionated from light to heavy REE. The REE concentrations in biotite and muscovite are high and indigenous. The pegmatite tourmalines contain low concentrations of REE. Variations in tourmaline REE patterns reflect the geochemical evolution of pegmatite melt/fluid system during crystallization.

  14. Synthesis of mesoporous Bi{sub 2}O{sub 3}/CeO{sub 2} microsphere for photocatalytic degradation of Orange II dye

    SciTech Connect (OSTI)

    Hsieh, Shu-Han; Manivel, Arumugam; Lee, Gang-Juan; Wu, Jerry J.

    2013-10-15

    Graphical abstract: - Highlights: Bi{sub 2}O{sub 3}/CeO{sub 2} microspheres were successfully synthesized by a hydrothermal procedure. Bi{sub 2}O{sub 3}/CeO{sub 2} microspheres were used to remove wastewater pollutant containing azo dye. The activity of Bi{sub 2}O{sub 3}/CeO{sub 2} is synergically enhanced compared to its pristine forms. - Abstract: We report on the visible-light responsive porous assembly of Bi{sub 2}O{sub 3}/CeO{sub 2} microspheres, which were synthesized via a simple hydrothermal reaction between Bi(NO{sub 3}){sub 3}5H{sub 2}O and Ce(NO{sub 3}){sub 3}6H{sub 2}O in the presence of ethylene glycol and ethanol. Systematic structural (X-ray diffraction (XRD)), morphological (field emission scanning electron microscopy (FE-SEM) and transmission electron microscopic (TEM)), BET surface area and diffuse reflectance spectral (DRS) analyses were carried out to characterize the formed product. The effects of experimental parameters on the microstructural and morphological behavior of Bi{sub 2}O{sub 3}/CeO{sub 2} composites were discussed. The semiconductor material as obtained was evaluated as a heterogeneous photocatalyst for the photolytic degradation of an azo dye in water and the degradation was found to follow pseudo-first-order rate kinetics. The study compares the rate constants of the new hybrid catalyst to a pristine Bi{sub 2}O{sub 3} and CeO{sub 2}, which has excellent catalytic properties under visible light irradiation for the degradation of Orange II dye.

  15. Fabrication and microstructure of cerium doped lutetium aluminum garnet (Ce:LuAG) transparent ceramics by solid-state reaction method

    SciTech Connect (OSTI)

    Li, Junlang; Xu, Jian; Shi, Ying; Qi, Hongfang; Xie, Jianjun; Lei, Fang

    2014-07-01

    Highlights: We fabricate Ce doped lutetium aluminum garnet ceramics by solid-state method. The raw materials include Lu{sub 2}O{sub 3} nanopowders synthesized by co-precipitation method. The density of the transparent ceramics reach 99.7% of the theoretical value. The optical transmittance of the bulk ceramic at 550 nm was 57.48%. Some scattering centers decrease the optical characteristic of the ceramic. - Abstract: Polycrystalline Ce{sup 3+} doped lutetium aluminum garnet (Ce:LuAG) transparent ceramics fabricated by one step solid-state reaction method using synthetic nano-sized Lu{sub 2}O{sub 3}, commercial ?-Al{sub 2}O{sub 3} and CeO{sub 2} powders were investigated in this paper. The green compacts shaped by the mixed powders were successfully densified into Ce:LuAG transparent ceramics after vacuum sintering at 1750 C for 10 h. The in-line optical transmittance of the Ce:LuAG ceramic made by home-made Lu{sub 2}O{sub 3} powders could reach 57.48% at 550 nm, which was higher than that of the ceramic made by commercial Lu{sub 2}O{sub 3} powders (22.96%). The microstructure observation showed that light scattering centers caused by micro-pores, aluminum segregation and refraction index inhomogeneities induced the decrease of optical transparency of the Ce:LuAG ceramics, which should be removed and optimized in the future work.

  16. Heavy fermion Ce{sub 3}Co{sub 4}Sn{sub 13} compound under pressure

    SciTech Connect (OSTI)

    Collave, J. R.; Borges, H. A.; Ramos, S. M.; Hering, E. N.; Mendona-Ferreira, L.; Pagliuso, P. G.

    2015-05-07

    The non-magnetic heavy fermion compound Ce{sub 3}Co{sub 4}Sn{sub 13} was studied under pressure. We report single crystalline measurements of electrical resistivity as a function of temperature ?(T) under pressure. Some characteristic features related to a structural transition (T{sub S}), crystalline field effects (T{sub CEF}), and a low temperature maximum (T{sub max}), possibly connected simultaneously to the onset of Kondo lattice coherence and short range magnetic correlations, were identified in the ?(T) data. A pressure-temperature phase diagram with T{sub S} and T{sub max} was constructed by mapping these features. Like for most Ce-based heavy fermion compounds, T{sub max} moves to higher temperatures with pressure, indicating that it is related to the Kondo energy scale, due to the increase of hybridization induced by pressure. On the other hand, T{sub S}, associated to a superlattice distortion and probably combined with a charge density wave transition, decreases as a function of pressure. However, differently from the Sr{sub 3?x}Ca{sub x}Ir{sub 4}Sn{sub 13} system, where a superlattice quantum phase transition is observed [L. E. Klintberg et al., Phys. Rev. Lett. 109, 237?008 (2012)], in Ce{sub 3}Co{sub 4}Sn{sub 13} T{sub S}???154?K, at ambient pressure (P?=?0), seems to stabilize at around 143?K for P???19 kilobars. We also investigated ?(T) in external magnetic fields, at P?=?0. Negative magnetoresistance and increase of T{sub max} are observed, suggesting suppression of low temperature short range magnetic correlations.

  17. Comparative Gamma Spectroscopy with SrI2(Eu), GYGAG(Ce) and Bi-loaded Plastic Scintillators

    SciTech Connect (OSTI)

    Cherepy, N J

    2010-11-19

    We are developing new scintillator materials that offer potential for high resolution gamma ray spectroscopy at low cost. Single crystal SrI{sub 2}(Eu) offers {approx}3% resolution at 662 keV, in sizes of {approx}1 in{sup 3}. We have developed ceramics processing technology allowing us to achieve cubic inch scale transparent ceramic scintillators offering gamma spectroscopy performance superior to NaI(Tl). We fabricated a bismuth-loaded plastic scintillator that demonstrates energy resolution of {approx}8% at 662 keV in small sizes. Gamma ray spectroscopy can be used to identify the presence of weak radioactive sources within natural background. The ability to discriminate close-lying spectral lines is strongly dependent upon the energy resolution of the detector. In addition to excellent energy resolution, large volume detectors are needed to acquire sufficient events, for example, to identify a radioactive anomaly moving past a detector. We have employed a 'directed search' methodology for identifying potential scintillator materials candidates, resulting in the discovery of Europium-doped Strontium Iodide, SrI{sub 2}(Eu), Cerium-doped Gadolinium Garnet, GYGAG(Ce), and Bismuth-loaded Polymers. These scintillators possess very low self-radioactivity, offer energy resolution of 3-8% at 662 keV, and have potential to be grown cost-effectively to sizes similar to the most widely deployed gamma spectroscopy scintillator, Thallium-doped Sodium Iodide, NaI(Tl). In this study, gamma ray spectra of a variety of sources, were obtained employing SrI{sub 2}(Eu), GYGAG(Ce), Bi-loaded polymers, LaBr{sub 3}(Ce), and NaI(Tl). The effects of detector size, energy resolution, and background radioactivity (including self-radioactivity) on the ability to distinguish weak sources is quantified, based on a simple model, and qualitatively compared to laboratory data.

  18. Effect of magnetic fields on the Kondo insulator CeRhSb: Magnetoresistance and high-field heat capacity measurements

    SciTech Connect (OSTI)

    Malik, S.K.; Menon, L.; Pecharsky, V.K.; Gschneidner, K.A. Jr.

    1997-05-01

    The compound CeRhSb is a mixed valent Ce-based compound which shows a gap in the electronic density of states at low temperatures. The gap manifests by a rise in electrical resistivity{emdash}below about 8 K from which the gap energy is estimated to be about 4 K. We have carried out heat capacity measurements on this compound in various applied fields up to 9.85 T. The magnetic contribution to the heat capacity, {Delta}C, is found to have a maximum in {Delta}C/T vs T at 10 K, below which {Delta}C/T is linear with T. This is attributed to the fact that below this temperature, in the gapped state, the electronic density of states decreases linearly with decreasing temperature. On application of a magnetic field, the electronic specific heat coefficient {gamma} in the gapped state increases by {approximately}4mJ/molK{sup 2}. The maximum in {Delta}C/T vs T is observed in all fields, which shifts to lower temperatures {approximately}1K at 5.32 T and raises again at 9.85 T to about the same values as at H=0T. This suggests that the gap exists for all fields up to 9.85 T. Above 10 K, in the mixed-valent state, {Delta}C/T vs T decreases with increasing temperature in zero field. There is hardly any effect of application of field in the mixed-valent state. We have also carried out magnetoresistance measurements on CeRhSb up to fields of 5.5 T at 2, 4.5, 10, 20, and 30 K. The magnetoresistance in CeRhSb is positive at temperatures of 4.5 K and above, in applied fields up to 5.5 T. At 5.5 T, the magnetoresistance is maximum at 4.5 K (6{percent}) and decreases with increasing temperature. The observation of the maximum is consistent with the observation of a maximum in {Delta}C/T vs T and is due to a change in the density of states. At a temperature of 2 K, a negative magnetoresistance is observed for magnetic fields greater than {approximately}3.5T which suggests reduction in the gap. {copyright} {ital 1997} {ital The American Physical Society}

  19. Response of LaBr{sub 3}(Ce) scintillators to 2.5 MeV fusion neutrons

    SciTech Connect (OSTI)

    Cazzaniga, C.; Nocente, M.; Gorini, G.; Istituto di Fisica del Plasma, Associazione EURATOM-ENEA-CNR, Via Roberto Cozzi 53, Milano 20125 ; Tardocchi, M.; Croci, G.; Giacomelli, L.; Angelone, M.; Pillon, M.; Villari, S.; Weller, A.; Petrizzi, L.; Collaboration: ASDEX Upgrade Team; JET-EFDA Contributors

    2013-12-15

    Measurements of the response of LaBr{sub 3}(Ce) to 2.5 MeV neutrons have been carried out at the Frascati Neutron Generator and at tokamak facilities with deuterium plasmas. The observed spectrum has been interpreted by means of a Monte Carlo model. It is found that the main contributor to the measured response is neutron inelastic scattering on {sup 79}Br, {sup 81}Br, and {sup 139}La. An extrapolation of the count rate response to 14 MeV neutrons from deuterium-tritium plasmas is also presented. The results are of relevance for the design of ?-ray diagnostics of fusion burning plasmas.

  20. Active Layer Soil Carbon and Nutrient Mineralization, Barrow, Alaska, 2012

    DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

    Stan D. Wullschleger; Holly M. Vander Stel; Colleen Iversen; Victoria L. Sloan; Richard J. Norby; Mallory P. Ladd; Jason K. Keller; Ariane Jong; Joanne Childs; Deanne J. Brice

    2015-10-29

    This data set consists of bulk soil characteristics as well as carbon and nutrient mineralization rates of active layer soils manually collected from the field in August, 2012, frozen, and then thawed and incubated across a range of temperatures in the laboratory for 28 day periods in 2013-2015. The soils were collected from four replicate polygons in each of the four Areas (A, B, C, and D) of Intensive Site 1 at the Next-Generation Ecosystem Experiments (NGEE) Arctic site near Barrow, Alaska. Soil samples were coincident with the established Vegetation Plots that are located in center, edge, and trough microtopography in each polygon. Data included are 1) bulk soil characteristics including carbon, nitrogen, gravimetric water content, bulk density, and pH in 5-cm depth increments and also by soil horizon, 2) carbon, nitrogen, and phosphorus mineralization rates for soil horizons incubated aerobically (and in one case both aerobically and anaerobically) for 28 days at temperatures that included 2, 4, 8, and 12 degrees C. Additional soil and incubation data are forthcoming. They will be available when published as part of another paper that includes additional replicate analyses.

  1. Fly ash and coal mineral matter surface transformations during heating

    SciTech Connect (OSTI)

    Baer, D R; Smith, R D

    1982-05-01

    A study is reported of surface segregation phenomena for fly ash and aluminosilicates representative of coal mineral matter during heating. The materials studied included a 20-..mu..m average diameter fly ash powder, a glass prepared from the fly ash, and Ca- and K-rich aluminosilicate minerals. The samples were heated both in air and under vacuum for extended periods at temperatures up to 1100/sup 0/C. XPS, Auger and SIMS methods were used to obtain relative surface elemental concentrations for major and minor components and depth profiles for some of the samples. Major differences were noted between samples heated in air (oxidizing) and those heated in vacuum (reducing) environments. For the fly ash glass heated in air Fe, Ti and Mg become enriched on the surfaces while heating in vacuum leads to Si surface segregation. Different trends upon heating were also observed for the Ca- and K-rich aluminosilicates. The results indicate two levels of surface enrichment upon the fly ash glass; a thin (< 500 A) layer and a thicker (1- to 2-..mu..m) layer most evident for heating in air where an Fe-rich layer is formed. The present results indicate that the rates of surface segregation may not be sufficiently fast on the time scale of fly ash formation to result in equilibrium surface segregation. It is concluded that condensation processes during fly ash formation probably play a major role in the observed fly ash surface enrichments.

  2. Generation and reactivity of putative support systems, Ce-Al neutral binary oxide nanoclusters: CO oxidation and CH bond activation

    SciTech Connect (OSTI)

    Wang, Zhe-Chen; Yin, Shi; Bernstein, Elliot R.

    2013-11-21

    Both ceria (CeO{sub 2}) and alumina (Al{sub 2}O{sub 3}) are very important catalyst support materials. Neutral binary oxide nanoclusters (NBONCs), Ce{sub x}Al{sub y}O{sub z}, are generated and detected in the gas phase and their reactivity with carbon monoxide (CO) and butane (C{sub 4}H{sub 10}) is studied. The very active species CeAlO{sub 4}{sup } can react with CO and butane via O atom transfer (OAT) and H atom transfer (HAT), respectively. Other Ce{sub x}Al{sub y}O{sub z} NBONCs do not show reactivities toward CO and C{sub 4}H{sub 10}. The structures, as well as the reactivities, of Ce{sub x}Al{sub y}O{sub z} NBONCs are studied theoretically employing density functional theory (DFT) calculations. The ground state CeAlO{sub 4}{sup } NBONC possesses a kite-shaped structure with an O{sub t}CeO{sub b}O{sub b}AlO{sub t} configuration (O{sub t}, terminal oxygen; O{sub b}, bridging oxygen). An unpaired electron is localized on the O{sub t} atom of the AlO{sub t} moiety rather than the CeO{sub t} moiety: this O{sub t} centered radical moiety plays a very important role for the reactivity of the CeAlO{sub 4}{sup } NBONC. The reactivities of Ce{sub 2}O{sub 4}, CeAlO{sub 4}{sup }, and Al{sub 2}O{sub 4} toward CO are compared, emphasizing the importance of a spin-localized terminal oxygen for these reactions. Intramolecular charge distributions do not appear to play a role in the reactivities of these neutral clusters, but could be important for charged isoelectronic BONCs. DFT studies show that the reaction of CeAlO{sub 4}{sup } with C{sub 4}H{sub 10} to form the CeAlO{sub 4}HC{sub 4}H{sub 9}{sup } encounter complex is barrierless. While HAT processes have been previously characterized for cationic and anionic oxide clusters, the reported study is the first observation of a HAT process supported by a ground state neutral oxide cluster. Mechanisms for catalytic oxidation of CO over surfaces of Al{sub x}O{sub y}/M{sub m}O{sub n} or M{sub m}O{sub n}/Al{sub x}O{sub y} materials are proposed consistent with the presented experimental and theoretical results.

  3. Antiferromagnetic Kondo lattice in the layered compound CePd1–xBi₂ and comparison to the superconductor LaPd1–xBi₂

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Han, Fei; Wan, Xiangang; Phelan, Daniel; Stoumpos, Constantinos C.; Sturza, Mihai; Malliakas, Christos D.; Li, Qing'an; Han, Tian-Heng; Zhao, Qingbiao; Chung, Duck Young; et al

    2015-07-13

    The layered compound CePd1–xBi₂ with the tetragonal ZrCuSi₂-type structure was obtained from excess Bi flux. Magnetic susceptibility data of CePd1–xBi₂ show an antiferromagnetic ordering below 6 K and are anisotropic along the c axis and the ab plane. The anisotropy is attributed to crystal-electric-field (CEF) effects and a CEF model which is able to describe the susceptibility data is given. An enhanced Sommerfeld coefficient γ of 0.191 J mol Ce⁻¹ K⁻² obtained from specific-heat measurement suggests a moderate Kondo effect in CePd1–xBi₂. Other than the antiferromagnetic peak at 6 K, the resistivity curve shows a shoulderlike behavior around 75 Kmore » which could be attributed to the interplay between Kondo and CEF effects. Magnetoresistance and Hall-effect measurements suggest that the interplay reconstructs the Fermi-surface topology of CePd1–xBi₂ around 75 K. Electronic structure calculations reveal that the Pd vacancies are important to the magnetic structure and enhance the CEF effects which quench the orbital moment of Ce at low temperatures.« less

  4. Electronic and optical properties of layered RE{sub 2}Ti{sub 2}O{sub 7} (RE = Ce and Pr) from first principles

    SciTech Connect (OSTI)

    Sayede, A.; Khenata, R.; Chahed, A.; Benhelal, O.

    2013-05-07

    We have studied the structural and electronic properties of Ce{sub 2}Ti{sub 2}O{sub 7} (CeTO) and Pr{sub 2}Ti{sub 2}O{sub 7} (PrTO) by first-principles density functional theory calculations. The computed structural parameters are in fairly good agreement with the available experimental findings. Band structure calculations using the GGA+U approach predict an insulating ground state for the herein studied compounds. The insulating band gaps of 2.00 eV and 2.83 eV are found for CeTO and PrTO, respectively. The analysis of the density of states reveals that the strongly localized RE 4f levels act as charge-trapping sites, predicting a lower photocatalytic activity for CeTO. We have also calculated the optical properties for both CeTO and PrTO. Based on these properties, it is predicted that these titanates are insensitive to ultra-violet radiation, while they are more sensitive to frequencies of the radiation in visible and early UV regions.

  5. Rapid Microwave Preparation of Highly Efficient Ce[superscript 3+]-Substituted Garnet Phosphors for Solid State White Lighting

    SciTech Connect (OSTI)

    Birkel, Alexander; Denault, Kristin A.; George, Nathan C.; Doll, Courtney E.; Hry, Bathylle; Mikhailovsky, Alexander A.; Birkel, Christina S.; Hong, Byung-Chul; Seshadri, Ram (UCSB); (Mitsubishi)

    2012-04-30

    Ce{sup 3+}-substituted aluminum garnet compounds of yttrium (Y{sub 3}Al{sub 5}O{sub 12}) and lutetium (Lu{sub 3}Al{sub 5}O{sub 12}) - both important compounds in the generation of (In,Ga)N-based solid state white lighting - have been prepared using a simple microwave heating technique involving the use of a microwave susceptor to provide the initial heat source. Carbon used as the susceptor additionally creates a reducing atmosphere around the sample that helps stabilize the desired luminescent compound. High quality, phase-pure materials are prepared within a fraction of the time and using a fraction of the energy required in a conventional ceramic preparation; the microwave technique allows for a reduction of about 95% in preparation time, making it possible to obtain phase pure, Ce{sup 3+}-substituted garnet compounds in under 20 min of reaction time. It is estimated that the overall reduction in energy compared with ceramic routes as practiced in the lab is close to 99%. Conventionally prepared material is compared with material prepared using microwave heating in terms of structure, morphology, and optical properties, including quantum yield and thermal quenching of luminescence. Finally, the microwave-prepared compounds have been incorporated into light-emitting diode 'caps' to test their performance characteristics in a real device, in terms of their photon efficiency and color coordinates.

  6. Effect of Doping on Surface Reactivity and Conduction Mechanism in Sm-doped CeO2 Thin Films

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Yang, Nan; Belianinov, Alex; Strelcov, Evgheni; Tebano, Antonello; Daniele, Dr. Di Castro; Schlueter, Dr. Christoph; Lee, Dr. Tien-Lin; Baddorf, Arthur P; Wisinger, Nina; Jesse, Stephen; et al

    2014-01-01

    Scanning probe microscopy measurements show irreversible surface electrochemistry in Sm-doped CeO2 thin films, which depends on humidity, temperature and doping concentration. A systematic study by electrochemical strain microscopy (ESM) in samples with two different Sm content and in several working conditions allows disclosing the microscopic mechanism underlying the difference in water adsorption and splitting with subsequent proton liberation. We measure the behavior of the hysteresis loops by changing temperature and humidity, both in standard ESM configuration and using the first order reversal curve (FORC) method. Complementing our study with spectroscopic measurements by hard x-ray photoemission spectroscopy we find that watermore » incorporation is favored until the doping with Sm is too high to allow the presence of Ce3+. The influence of doping on the surface reactivity and conduction mechanism clearly emerges from all of our experimental results. We find that at lower Sm concentration proton conduction is prevalent, featured by lower activation energy and higher mobility. Defect concentrations determine the type of the prevalent charge carrier in a doping dependent manner.« less

  7. Method for the Production of Mineral Wool andIron from Serpentine Ore

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Method for the Production of Mineral Wool and Iron from Serpentine Ore Overview This invention discloses a method to fabricate a product that has the potential to replace asbestos, which harbors health and environmental risks, with magnesium silicate-based mineral wools. The mineral wool product yields advantages similar to asbestos while eliminating its inherent detriments. Since the late 19th century and into the late 20th century, asbestos has been a commonly used building material for home

  8. Quantitative determination of mineral composition by powder X-ray diffraction

    DOE Patents [OSTI]

    Pawloski, Gayle A. (Livermore, CA)

    1986-01-01

    An external standard intensity ratio method is used for quantitatively determining mineralogic compositions of samples by x-ray diffraction. The method uses ratios of x-ray intensity peaks from a single run. Constants are previously determined for each mineral which is to be quantitatively measured. Ratios of the highest intensity peak of each mineral to be quantified in the sample and the highest intensity peak of a reference mineral contained in the sample are used to calculate sample composition.

  9. Method for the Production of Mineral Wool and Iron from Serpentine Ore -

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    Energy Innovation Portal Industrial Technologies Industrial Technologies Building Energy Efficiency Building Energy Efficiency Advanced Materials Advanced Materials Find More Like This Return to Search Method for the Production of Mineral Wool and Iron from Serpentine Ore Magnesium silicate-based mineral wool insulation National Energy Technology Laboratory Contact NETL About This Technology Publications: PDF Document Publication Partnership Opportunity Notice for Mineral Wool (331 KB) PDF

  10. Quantitative determination of mineral composition by powder x-ray diffraction

    DOE Patents [OSTI]

    Pawloski, G.A.

    1984-08-10

    An external standard intensity ratio method is used for quantitatively determining mineralogic compositions of samples by x-ray diffraction. The method uses ratios of x-ray intensity peaks from a single run. Constants are previously determined for each mineral which is to be quantitatively measured. Ratios of the highest intensity peak of each mineral to be quantified in the sample and the highest intensity peak of a reference mineral contained in the sample are used to calculate sample composition.

  11. Composition and method for self-assembly and mineralization of peptide amphiphiles

    DOE Patents [OSTI]

    Stupp, Samuel I. (Chicago, IL); Beniash, Elia (Newton, MA); Hartgerink, Jeffrey D. (Houston, TX)

    2009-06-30

    The present invention is directed to a composition useful for making homogeneously mineralized self assembled peptide-amphiphile nanofibers and nanofiber gels. The composition is generally a solution comprised of a positively or negatively charged peptide-amphiphile and a like signed ion from the mineral. Mixing this solution with a second solution containing a dissolved counter-ion of the mineral and/or a second oppositely charged peptide amphiphile, results in the rapid self assembly of the peptide-amphiphiles into a nanofiber gel and templated mineralization of the ions. Templated mineralization of the initially dissolved mineral cations and anions in the mixture occurs with preferential orientation of the mineral crystals along the fiber surfaces within the nanofiber gel. One advantage of the present invention is that it results in homogenous growth of the mineral throughout the nanofiber gel. Another advantage of the present invention is that the nanofiber gel formation and mineralization reactions occur in a single mixing step and under substantially neutral or physiological pH conditions. These homogeneous nanostructured composite materials are useful for medical applications especially the regeneration of damaged bone in mammals. This invention is directed to the synthesis of peptide-amphiphiles with more than one amphiphilic moment and to supramolecular compositions comprised of such multi-dimensional peptide-amphiphiles. Supramolecular compositions can be formed by self assembly of multi-dimensional peptide-amphiphiles by mixing them with a solution comprising a monovalent cation.

  12. Composition and method for self-assembly and mineralization of peptide-amphiphiles

    DOE Patents [OSTI]

    Stupp, Samuel I. (Chicago, IL); Beniash, Elia (Newton, MA); Hartgerink, Jeffrey D. (Pearland, TX)

    2012-02-28

    The present invention is directed to a composition useful for making homogeneously mineralized self assembled peptide-amphiphile nanofibers and nanofiber gels. The composition is generally a solution comprised of a positively or negatively charged peptide-amphiphile and a like signed ion from the mineral. Mixing this solution with a second solution containing a dissolved counter-ion of the mineral and/or a second oppositely charged peptide amphiphile, results in the rapid self assembly of the peptide-amphiphiles into a nanofiber gel and templated mineralization of the ions. Templated mineralization of the initially dissolved mineral cations and anions in the mixture occurs with preferential orientation of the mineral crystals along the fiber surfaces within the nanofiber gel. One advantage of the present invention is that it results in homogenous growth of the mineral throughout the nanofiber gel. Another advantage of the present invention is that the nanofiber gel formation and mineralization reactions occur in a single mixing step and under substantially neutral or physiological pH conditions. These homogeneous nanostructured composite materials are useful for medical applications especially the regeneration of damaged bone in mammals. This invention is directed to the synthesis of peptide-amphiphiles with more than one amphiphilic moment and to supramolecular compositions comprised of such multi-dimensional peptide-amphiphiles. Supramolecular compositions can be formed by self assembly of multi-dimensional peptide-amphiphiles by mixing them with a solution comprising a monovalent cation.

  13. Fundamental study of CO2-H2O-mineral interactions for carbon...

    Office of Scientific and Technical Information (OSTI)

    E.; Wang, Yifeng; Matteo, Edward N.; Meserole, Stephen P.; Tallant, David Robert In the supercritical CO2-water-mineral systems relevant to subsurface CO2 sequestration,...

  14. Plutonium Oxidation and Subsequent Reduction by Mn (IV) Minerals

    SciTech Connect (OSTI)

    KAPLAN, DANIEL

    2005-09-13

    Plutonium sorbed to rock tuff was preferentially associated with manganese oxides. On tuff and synthetic pyrolusite (Mn{sup IV}O{sub 2}), Pu(IV) or Pu(V) was initially oxidized, but over time Pu(IV) became the predominant oxidation state of sorbed Pu. Reduction of Pu(V/VI), even on non-oxidizing surfaces, is proposed to result from a lower Gibbs free energy of the hydrolyzed Pu(IV) surface species versus that of the Pu(V) or Pu(VI) surface species. This work suggests that despite initial oxidation of sorbed Pu by oxidizing surfaces to more soluble forms, the less mobile form of Pu, Pu(IV), will dominate Pu solid phase speciation during long term geologic storage. The safe design of a radioactive waste or spent nuclear fuel geologic repository requires a risk assessment of radionuclides that may potentially be released into the surrounding environment. Geochemical knowledge of the radionuclide and the surrounding environment is required for predicting subsurface fate and transport. Although difficult even in simple systems, this task grows increasingly complicated for constituents, like Pu, that exhibit complex environmental chemistries. The environmental behavior of Pu can be influenced by complexation, precipitation, adsorption, colloid formation, and oxidation/reduction (redox) reactions (1-3). To predict the environmental mobility of Pu, the most important of these factors is Pu oxidation state. This is because Pu(IV) is generally 2 to 3 orders of magnitude less mobile than Pu(V) in most environments (4). Further complicating matters, Pu commonly exists simultaneously in several oxidation states (5, 6). Choppin (7) reported Pu may exist as Pu(IV), Pu(V), or Pu(VI) oxic natural groundwaters. It is generally accepted that plutonium associated with suspended particulate matter is predominantly Pu(IV) (8-10), whereas Pu in the aqueous phase is predominantly Pu(V) (2, 11-13). The influence of the character of Mn-containing minerals expected to be found in subsurface repository environments on Pu oxidation state distributions has been the subject of much recent research. Kenney-Kennicutt and Morse (14), Duff et al. (15), and Morgenstern and Choppin (16) observed oxidation of Pu facilitated by Mn(IV)-bearing minerals. Conversely, Shaughnessy et al. (17) used X-ray Absorption near-edge spectroscopy (XANES) to show reduction of Pu(VI) by hausmannite (Mn{sup II}Mn{sub 2}{sup III}O{sub 4}) and manganite ({gamma}-Mn{sup III}OOH) and Kersting et al., (18) observed reduction of Pu(VI) by pyrolusite (Mn{sup IV}O{sub 2}). In this paper, we attempt to reconcile the apparently conflicting datasets by showing that Mn-bearing minerals can indeed oxidize Pu, however, if the oxidized species remains on the solid phase, the oxidation step competes with the formation of Pu(IV) that becomes the predominant solid phase Pu species with time. The experimental approach we took was to conduct longer term (approximately two years later) oxidation state analyses on the Pu sorbed to Yucca Mountain tuff (initial analysis reported by Duff et al., (15)) and measure the time-dependant changes in the oxidation state distribution of Pu in the presence of the Mn mineral pyrolusite.

  15. Catalytic effects of minerals on NOx emission from coal combustion

    SciTech Connect (OSTI)

    Yao, M.Y.; Che, D.F.

    2007-07-01

    The catalytic effects of inherent mineral matters on NOx emissions from coal combustion have been investigated by a thermo-gravimetric analyzer (TGA) equipped with a gas analyzer. The effect of demineralization and the individual effect of Na, K, Ca, Mg, and Fe on the formation of NOx are studied as well as the combined catalytic effects of Ca + Na and Ca + Ti. Demineralization causes more Fuel-N to retain in the char, and reduction of NOx mostly. But the mechanistic effect on NOx formation varies from coal to coal. Ca and Mg promote NOx emission. Na, K, Fe suppress NOx formation to different extents. The effect of transition element Fe is the most obvious. The combination of Ca + Na and Ca + Ti can realize the simultaneous control of sulfur dioxide and nitrogen oxides emissions.

  16. Utilization of coal-associated minerals. Final report

    SciTech Connect (OSTI)

    Slonaker, J. F.; Akers, D. J.; Alderman, J. K.

    1980-01-01

    Under contract number DE-AS21-77ET10533 with the US-DOE several methods of utilizing coal associated by-products were examined for potential commercial use. Such use could transform a costly waste disposal situation into new materials for further use and could provide incentive for the adoption of new coal utilization processes. Several utilization processes appear to have merit and are recommended for further study. Each process is discussed separately in the text of this report. Common coal cleaning processes were also examined to determine the effect of such processes on the composition of by-products. Data obtained in this portion of the research effort are reported in the Appendix. Information of this type is required before utilization processes can be considered. A knowledge of the mineral composition of these materials is also required before even simple disposal methods can be considered.

  17. Osage oil: Mineral law, murder, mayhem, and manipulation

    SciTech Connect (OSTI)

    Strickland, R.

    1995-12-31

    The greatest of the 20th century Osage chiefs, Fred Lookout, feared what the rich oil bonanza under tribal lands would do to his people. He forsaw that oil wealth could turn into a curse as well as a blessing, and it was both. The story of Osage oil is a case history in the failure of law, the failure of Indian policy and the struggle for survival of the indomitable spirit of a great Native people force to deal with both the curse and the blessing of black gold. This article examines law and policy as seen in Osage oil regulation, outlining the legal controls of the land and mineral regulatory system and briefly exploring the breakdowns of the system.

  18. Chemical Reduction of Nd 1.85 Ce 0.15 CuO 4− δ Powders in Supercritical Sodium Ammonia Solutions

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Dias, Yasmin; Wang, Hui; Zhou, Haiqing; Lin, Feng; Lan, Yucheng

    2015-01-01

    Nd 1.85 Ce 0.15 CuO 4− δ powders are chemically reduced in supercritical sodium ammonia solutions from room temperature to 350°C. The crystallographic structure of the reduced powders is investigated from Rietveld refinement of X-ray powder diffraction. The atomic positions are maintained constant within experimental errors while temperature factors of all atoms increase significantly after the chemical treatments, especially of Nd/Ce atoms. The ammonothermally reduced Nd 1.85 Ce 0.15 CuO 4− δ powders show diamagnetic below 24 K which is contributed to the lower oxygen content and higher temperature factors of atoms in the treated compound.more » The ammonothermal method paves a new way to reduce oxides in supercritical solutions near room temperature.« less

  19. Chemical Reduction of Nd1.85Ce0.15CuO4??Powders in Supercritical Sodium Ammonia Solutions

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Dias, Yasmin; Wang, Hui; Zhou, Haiqing; Lin, Feng; Lan, Yucheng

    2015-01-01

    Nd1.85Ce0.15CuO4??powders are chemically reduced in supercritical sodium ammonia solutions from room temperature to 350C. The crystallographic structure of the reduced powders is investigated from Rietveld refinement of X-ray powder diffraction. The atomic positions are maintained constant within experimental errors while temperature factors of all atoms increase significantly after the chemical treatments, especially of Nd/Ce atoms. The ammonothermally reduced Nd1.85Ce0.15CuO4??powders show diamagnetic below 24?K which is contributed to the lower oxygen content and higher temperature factors of atoms in the treated compound. The ammonothermal method paves a new way to reduce oxides in supercritical solutions near room temperature.

  20. Pressure-Induced Structural Phase Transition in CeNi: X-ray and Neutron Scattering Studies and First-Principles Calculations

    SciTech Connect (OSTI)

    Mirmelstein, A.; Podlesnyak, Andrey A.; dos Santos, Antonio M.; Ehlers, Georg; Kerbel, O.; Matvienko, V.; Sefat, A. S.; Saporov, B.; Halder, G. J.; Tobin, J. G.

    2015-08-03

    The pressure-induced structural phase transition in the intermediate-valence compound CeNi has been investigated by x-ray and neutron powder diffraction techniques. It is shown that the structure of the pressure-induced CeNi phase (phases) can be described in terms of the Pnma space group. Equations of state for CeNi on both sides of the phase transition are derived and an approximate P-T phase diagram is suggested for P<8 GPa and T<300 K. The observed Cmcm?Pnma structural transition is then analyzed using density functional theory calculations, which successfully reproduce the ground state volume, the phase transition pressure, and the volume collapse associated with the phase transition.

  1. Uranium mineralization in fluorine-enriched volcanic rocks

    SciTech Connect (OSTI)

    Burt, D.M.; Sheridan, M.F.; Bikun, J.; Christiansen, E.; Correa, B.; Murphy, B.; Self, S.

    1980-09-01

    Several uranium and other lithophile element deposits are located within or adjacent to small middle to late Cenozoic, fluorine-rich rhyolitic dome complexes. Examples studied include Spor Mountain, Utah (Be-U-F), the Honeycomb Hills, Utah (Be-U), the Wah Wah Mountains, Utah (U-F), and the Black Range-Sierra Cuchillo, New Mexico (Sn-Be-W-F). The formation of these and similar deposits begins with the emplacement of a rhyolitic magma, enriched in lithophile metals and complexing fluorine, that rises to a shallow crustal level, where its roof zone may become further enriched in volatiles and the ore elements. During initial explosive volcanic activity, aprons of lithicrich tuffs are erupted around the vents. These early pyroclastic deposits commonly host the mineralization, due to their initial enrichment in the lithophile elements, their permeability, and the reactivity of their foreign lithic inclusions (particularly carbonate rocks). The pyroclastics are capped and preserved by thick topaz rhyolite domes and flows that can serve as a source of heat and of additional quantities of ore elements. Devitrification, vapor-phase crystallization, or fumarolic alteration may free the ore elements from the glassy matrix and place them in a form readily leached by percolating meteoric waters. Heat from the rhyolitic sheets drives such waters through the system, generally into and up the vents and out through the early tuffs. Secondary alteration zones (K-feldspar, sericite, silica, clays, fluorite, carbonate, and zeolites) and economic mineral concentrations may form in response to this low temperature (less than 200 C) circulation. After cooling, meteoric water continues to migrate through the system, modifying the distribution and concentration of the ore elements (especially uranium).

  2. Reactivity of pulverized coals during combustion catalyzed by CeO{sub 2} and Fe{sub 2}O{sub 3}

    SciTech Connect (OSTI)

    Gong, Xuzhong; Guo, Zhancheng; Wang, Zhi

    2010-02-15

    Effects of CeO{sub 2} and Fe{sub 2}O{sub 3} on combustion reactivity of several fuels, including three ranks of coals, graphite and anthracite chars, were investigated using thermo-gravimetric analyzer. The results indicated that the combustion reactivity of all the samples except lignite was improved with CeO{sub 2} or Fe{sub 2}O{sub 3} addition. It was interesting to note that the ignition temperatures of anthracite were decreased by 50 C and 53 C, respectively, with CeO{sub 2} and Fe{sub 2}O{sub 3} addition and that its combustion rates were increased to 15.4%/min and 12.2%/min. Ignition temperatures of lignite with CeO{sub 2} and Fe{sub 2}O{sub 3} addition were 250 C and 226 C, and the combustion rates were 12.8% and 19.3%/min, respectively. When compared with those of lignite without catalysts, no obvious catalytic effects of the two catalysts on its combustion reactivity were revealed. The results from the combustion of the three rank pulverized coals catalyzed by CeO{sub 2} and Fe{sub 2}O{sub 3} indicated significant effects of the two catalysts on fixed carbon combustion. And it was found that the higher the fuel rank, the better the catalytic effect. The results of combustion from two kinds of anthracite chars showed obvious effects of anthracite pyrolysis catalyzed by CeO{sub 2} and Fe{sub 2}O{sub 3} on its combustion reactivity. (author)

  3. Magnetic hardening of Ce1+xFe11–yCoyTi with ThMn12 structure by melt spinning

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Zhou, Chen; Sun, Kewei; Pinkerton, Frederick E.; Kramer, M. J.

    2015-04-15

    A recent study on the intrinsic magnetic properties of CeFe11–yCoyTi has revealed that substituting one Co for Fe retains the favorable magnetocrystalline anisotropy Ha found in the ternary Fe end member, while enhancing the Curie temperature Tc and saturation magnetization 4πMs. These findings warrant further optimization around Co substitution y = 1 to try to exploit the hard magnetic properties of these Ce-based magnets. Both Ce and Co concentrations in Ce1+xFe11–yCoyTi have been optimized in the range of x = 0 – 0.2 and y = 0 –1.5. It was found that Co substitution effectively enhances all hard magnetic properties,more »although the values are still lower than those predicted from the intrinsic magnetic properties. Specifically, Tc increases from 210 °C to 285 – 350 °C; 4πM19 (magnetization at 19 kOe) from 8.9 kG to 10.5 – 11.5 kG, remanence Br from 3.1 kG to 4.1 – 4.5 kG, and most importantly, Hci from 1.1 kOe to 1.5 kOe. As a result, the room temperature energy product (BH)max has been increased by over 100% from 0.7 MGOe in Ce1.1Fe11Ti to 1.5 MGOe in Ce1.05Fe9.75Co1.25Ti. Microscopy analysis indicates that the addition of Co refines the grain size and promotes chemical homogeneity at the microscopic scale. As a result, the beneficial effect of Co on the microstructure contributes to the improved hard magnetic properties.« less

  4. Magnetic hardening of Ce1+xFe11–yCoyTi with ThMn12 structure by melt spinning

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Zhou, Chen; Sun, Kewei; Pinkerton, Frederick E.; Kramer, M. J.

    2015-04-15

    A recent study on the intrinsic magnetic properties of CeFe11–yCoyTi has revealed that substituting one Co for Fe retains the favorable magnetocrystalline anisotropy Ha found in the ternary Fe end member, while enhancing the Curie temperature Tc and saturation magnetization 4πMs. These findings warrant further optimization around Co substitution y = 1 to try to exploit the hard magnetic properties of these Ce-based magnets. Both Ce and Co concentrations in Ce1+xFe11–yCoyTi have been optimized in the range of x = 0 – 0.2 and y = 0 –1.5. It was found that Co substitution effectively enhances all hard magnetic properties,more » although the values are still lower than those predicted from the intrinsic magnetic properties. Specifically, Tc increases from 210 °C to 285 – 350 °C; 4πM19 (magnetization at 19 kOe) from 8.9 kG to 10.5 – 11.5 kG, remanence Br from 3.1 kG to 4.1 – 4.5 kG, and most importantly, Hci from 1.1 kOe to 1.5 kOe. As a result, the room temperature energy product (BH)max has been increased by over 100% from 0.7 MGOe in Ce1.1Fe11Ti to 1.5 MGOe in Ce1.05Fe9.75Co1.25Ti. Microscopy analysis indicates that the addition of Co refines the grain size and promotes chemical homogeneity at the microscopic scale. As a result, the beneficial effect of Co on the microstructure contributes to the improved hard magnetic properties.« less

  5. Lu.sub.1-xI.sub.3:Ce.sub.x-a scintillator for gamma-ray spectroscopy and time-of-flight pet

    DOE Patents [OSTI]

    Shah, Kanai S.

    2008-02-12

    The present invention includes very fast scintillator materials including lutetium iodide doped with Cerium (Lu.sub.1-xI.sub.3:Ce.sub.x; LuI.sub.3:Ce). The LuI.sub.3 scintillator material has surprisingly good characteristics including high light output, high gamma-ray stopping efficiency, fast response, low cost, good proportionality, and minimal afterglow that the material is useful for gamma-ray spectroscopy, medical imaging, nuclear and high energy physics research, diffraction, non-destructive testing, nuclear treaty verification and safeguards, and geological exploration.

  6. Applications of scanning electron microscopy to the study of mineral matter in peat

    SciTech Connect (OSTI)

    Raymond, R. Jr.; Andrejko, M.J.; Bardin, S.W.

    1983-01-01

    Scanning electron microscopy (SEM) and energy dispersive spectrometry (EDS) have been used for in situ analysis of minerals in peats by combining methods for producing oriented microtome sections of peat with methods for critical point drying. The combined technique allows SEM analysis of the inorganic components and their associated botanical constituents, along with petrographic identification of the botanical constituents. In peat deposits with abundant fluvial- or marine-derived minerals, one may use the above technique and/or medium- or low-temperature ashing followed by x-ray diffraction to readily identify the various mineral components. However, in some freshwater environments the scarcity of non-silica minerals makes the above techniques impractical. By separating the inorganic residues from the peat, one can isolate the non-silica mineral matter in the SEM for analysis by EDS. Furthermore, such separation allows SEM analysis of features and textures of both silica and non-silica mineral particles that might otherwise be unidentifiable. Results indicate the occurrence of detritial minerals in both Okefenokee and Snuggedy Swamp peats, the presence of authigenic or diagenetic minerals growing within peats, and dissolution features on freshwater sponge spicules that may account for the absence of spicules in Tertiary lignites.

  7. An epidemiological study of salt miners in diesel and nondiesel mines

    SciTech Connect (OSTI)

    Gamble, J.; Jones, W.; Hudak, J.

    1983-01-01

    A cross-sectional study of 5 NaCl mines and 259 miners addressed the following questions: 1) Is there an association of increased respiratory symptoms, radiographic findings, and reduced pulmonary function with exposure to nitrogen dioxide (NO2) and/or respirable particulate (RP) among these miners. 2) Is there increased morbidity of these miners compared to other working populations. Personal samples of NO2 and respirable particulate for jobs in each mine were used to estimate cumulative exposure. NO2 is used as a surrogate measure of diesel exposure. Cough was associated with age and smoking, dyspnea with age; neither symptom was associated with exposure (years worked, estimated cumulative NO2 or RP exposure). Phlegm was associated with age, smoking, and exposure. Reduced pulmonary function (FVC, FEV1, peak, flow, FEF50, FEF75) showed no association with exposure. There was one case of small rounded and one case of small irregular opacities; pneumoconiosis was not analyzed further. Compared to underground coal miners, above ground coal miners, potash miners, and nonmining workers, the study population after adjustment for age and smoking generally showed no increased prevalence of cough, phlegm, dyspnea, or obstruction (FEV1/FVC less than 0.7). Obstruction in younger salt miners and phlegm in older salt miners was elevated compared to nonmining workers. Mean predicted pulmonary function was reduced 2-4% for FEV1 and FVC, 7-13% for FEF50, and 18-22% for FEF75 below all comparison populations.

  8. A Novel Approach to Experimental Studies of Mineral Dissolution Kinetics

    SciTech Connect (OSTI)

    Chen Zhu

    2006-08-31

    Currently, DOE is conducting pilot CO{sub 2} injection tests to evaluate the concept of geological sequestration. One strategy that potentially enhances CO{sub 2} solubility and reduces the risk of CO{sub 2} leak back to the surface is dissolution of indigenous minerals in the geological formation and precipitation of secondary carbonate phases, which increases the brine pH and immobilizes CO{sub 2}. Clearly, the rates at which these dissolution and precipitation reactions occur directly determine the efficiency of this strategy. However, one of the fundamental problems in modern geochemistry is the persistent two to five orders of magnitude discrepancy between laboratory measured and field derived feldspar dissolution rates. To date, there is no real guidance as to how to predict silicate reaction rates for use in quantitative models. Current models for assessment of geological carbon sequestration have generally opted to use laboratory rates, in spite of the dearth of such data for compositionally complex systems, and the persistent disconnect between laboratory and field applications. Therefore, a firm scientific basis for predicting silicate reaction kinetics in CO2 injected geological formations is urgently needed to assure the reliability of the geochemical models used for the assessments of carbon sequestration strategies. The funded experimental and theoretical study attempts to resolve this outstanding scientific issue by novel experimental design and theoretical interpretation to measure silicate dissolution rates and iron carbonate precipitation rates at conditions pertinent to geological carbon sequestration. In the second year of the project, we completed CO{sub 2}-Navajo sandstone interaction batch and flow-through experiments and a Navajo sandstone dissolution experiment without the presence of CO{sub 2} at 200 C and 250-300 bars, and initiated dawsonite dissolution and solubility experiments. We also performed additional 5-day experiments at the same conditions as alkali-feldspar dissolution experiments with and without the presence of CO{sub 2} performed in the first year to check the validation of the experiments and analysis. The changes of solution chemistry as dissolution experiments progressed were monitored with on-line sampling of the aqueous phase at the constant temperature and pressure. These data allow calculating overall apparent mineral (feldspars and sandstones) dissolution rates and secondary mineral precipitation rates as a function of saturation states. State-of-the-art atomic resolution transmission electron microscopy (TEM), scanning electron microscopy (SEM), and electron microprobe was used to characterize the products and reactants. Reaction-path geochemical modeling was used to interpret the experimental results of alkali-feldspar dissolution experiments without the presence of CO{sub 2}. Two manuscripts are near completion. Also during the second year, our education goal of graduate student training has been advanced. A Ph. D. student at Indiana University is progressing well in the degree program and has taken geochemical modeling, SEM, and TEM courses, which will facilitate research in the third year. A Ph. D. student at University of Minnesota had graduated. With the success of training of graduate students and excellent experimental data in the second year, we anticipate a more fruitful year in the third year.

  9. High pressures and the Kondo gap in Ce{sub 3}Bi{sub 4}Pt{sub 3}

    SciTech Connect (OSTI)

    Cooley, J.C.; Aronson, M.C.; Canfield, P.C.

    1997-03-01

    We have measured the electrical resistivity {rho}(T) of single crystals of Ce{sub 3}Bi{sub 4}Pt{sub 3} for temperatures from 1.2 to 300 K, and pressures from 1 bar to 145 kbar. The transport is dominated at high temperatures by excitations across a small activation gap {Delta}, which increases rapidly with pressure. The low-temperature transport involves variable range hopping among extrinsic states in the gap. The spatial extent of the in-gap states reflects coupling to conduction-electron states, and is strongly modified as pressure enhances {Delta}. Despite the strong pressure dependence of {Delta}, a direct correspondence between single-ion energetics and the measured gap is maintained, and the role of valence fluctuations is minimal even at the highest pressures. {copyright} {ital 1997} {ital The American Physical Society}

  10. Magnetic properties of CeFe11-xCoxTi with ThMn12 structure

    SciTech Connect (OSTI)

    Zhou, C; Pinkerton, FE; Herbst, JF

    2014-05-07

    A series of novel alloys CeFe11-xCoxTi (0 <= x <= 11) with ThMn12 structure has been successfully prepared by melt-spinning. The Curie temperature T-c increases with Co content x, reaching a maximum of 689 degrees C at x = 9 and declining to 664 degrees C at complete Co filling (x = 11). The room temperature saturation magnetization 4 pi M-s and magnetocrystalline anisotropy H-a have been estimated by fitting the first quadrant demagnetization curve with the Stoner-Wohlfarth model. 4 pi M-s first increases with increasing Co up to x = 3, then decrease. H-a has a complex dependence on Co content, which is indicative of a change in the easy magnetization direction from axis to plane and back as the Co content increases. (C) 2014 AIP Publishing LLC.

  11. Low pressure CO₂ hydrogenation to methanol over gold nanoparticles activated on a CeOx/TiO₂ interface

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Yang, Xiaofang; Boscoboinik, J. Anibal; Kattel, Shyam; Senanayake, Sanjaya D.; Nie, Xiaowa; Graciani, Jesus; Rodriguez, Jose A.; Liu, Ping; Stacchiola, Dario J.; Chen, Jingguang G.

    2015-07-28

    Capture and recycling of CO₂ into valuable chemicals such as alcohols could help mitigate its emissions into the atmosphere. Due to its inert nature, the activation of CO₂ is a critical step in improving the overall reaction kinetics during its chemical conversion. Although pure gold is an inert noble metal and cannot catalyze hydrogenation reactions, it can be activated when deposited as nanoparticles on the appropriate oxide support. In this combined experimental and theoretical study, it is shown that an electronic polarization at the metal–oxide interface of Au nanoparticles anchored and stabilized on a CeOx/TiO₂ substrate generates active centers formore » CO₂ adsorption and its low pressure hydrogenation, leading to a higher selectivity toward methanol. In conclusion, this study illustrates the importance of localized electronic properties and structure in catalysis for achieving higher alcohol selectivity from CO₂ hydrogenation.« less

  12. Degradation of dome cutting minerals in Hanford waste

    SciTech Connect (OSTI)

    Reynolds, Jacob G.; Huber, Heinz J.; Cooke, Gary A.

    2013-01-11

    At the Hanford Tank Farms, recent changes in retrieval technology require cutting new risers in several single-shell tanks. The Hanford Tank Farm Operator is using water jet technology with abrasive silicate minerals such as garnet or olivine to cut through the concrete and rebar dome. The abrasiveness of these minerals, which become part of the high-level waste stream, may enhance the erosion of waste processing equipment. However, garnet and olivine are not thermodynamically stable in Hanford waste, slowly degrading over time. How likely these materials are to dissolve completely in the waste before the waste is processed in the Waste Treatment and Immobilization Plant can be evaluated using theoretical analysis for olivine and collected direct experimental evidence for garnet. Based on an extensive literature study, a large number of primary silicates decompose into sodalite and cancrinite when exposed to Hanford waste. Given sufficient time, the sodalite also degrades into cancrinite. Even though cancrinite has not been directly added to any Hanford tanks during process times, it is the most common silicate observed in current Hanford waste. By analogy, olivine and garnet are expected to ultimately also decompose into cancrinite. Garnet used in a concrete cutting demonstration was immersed in a simulated supernate representing the estimated composition of the liquid retrieving waste from Hanford tank 241-C-107 at both ambient and elevated temperatures. This simulant was amended with extra NaOH to determine if adding caustic would help enhance the degradation rate of garnet. The results showed that the garnet degradation rate was highest at the highest NaOH concentration and temperature. At the end of 12 weeks, however, the garnet grains were mostly intact, even when immersed in 2 molar NaOH at 80 deg C. Cancrinite was identified as the degradation product on the surface of the garnet grains. In the case of olivine, the rate of degradation in the high-pH regimes of a waste tank is expected to depend on two main parameters: carbonate is expected to slow olivine degradation rates, whereas hydroxide is expected to enhance olivine dissolution rates. Which of these two competing dissolution drivers will have a larger impact on the dissolution rate in the specific environment of a waste tank is currently not identifiable. In general, cancrinite is much smaller and less hard than either olivine or garnet, so would be expected to be less erosive to processing equipment. Complete degradation of either garnet or olivine prior to being processed at the Waste Treatment and Immobilization Plant cannot be confirmed, however.

  13. Analysis of stream sediment reconnaissance data for mineral resources from the Montrose NTMS Quadrangle, Colorado

    SciTech Connect (OSTI)

    Beyth, M.; Broxton, D.; McInteer, C.; Averett, W.R.; Stablein, N.K.

    1980-06-01

    Multivariate statistical analysis to support the National Uranium Resource Evaluation and to evaluate strategic and other commercially important mineral resources was carried out on Hydrogeochemical and Stream Sediment Reconnaissance data from the Montrose quadrangle, Colorado. The analysis suggests that: (1) the southern Colorado Mineral Belt is an area favorable for uranium mineral occurrences; (2) carnotite-type occurrences are likely in the nose of the Gunnison Uplift; (3) uranium mineral occurrences may be present along the western and northern margins of the West Elk crater; (4) a base-metal mineralized area is associated with the Uncompahgre Uplift; and (5) uranium and base metals are associated in some areas, and both are often controlled by faults trending west-northwest and north.

  14. Investigation of the physical properties of the tetragonal CeMAl4Si2 (M = Rh, Ir, Pt) compounds

    SciTech Connect (OSTI)

    Ghimire, N. J.; Ronning, F.; Williams, D. J.; Scott, B. L.; Luo, Yongkang; Thompson, J. D.; Bauer, E. D.

    2014-12-15

    The synthesis, crystal structure and physical properties studied by means of x-ray diffraction, magnetic, thermal and transport measurements of CeMAl4Si2 (M = Rh, Ir, Pt) are reported, along with the electronic structure calculations for LaMAl4Si2 (M = Rh, Ir, Pt). These materials adopt a tetragonal crystal structure (space group P4/mmm) comprised of BaAl4 blocks, separated by MAl2 units, stacked along the c-axis. Both CeRhAl4Si2 and CeIrAl4Si2 order antiferromagnetically below TN1 = 14 and 16 K, respectively, and undergo a second antiferromagnetic transitition at lower temperature (TN2 = 9 and 14 K, respectively). CePtAl4Si2 orders ferromagnetically below TC = 3 K with an ordered moment of ?sat = 0.8 ?B for a magnetic field applied perpendicular to the c-axis. Electronic structure calculations reveal quasi-2D character of the Fermi surface.

  15. Data:F3d511d9-6321-49ce-b5b2-a0d21fd28d52 | Open Energy Information

    Open Energy Info (EERE)

    d9-6321-49ce-b5b2-a0d21fd28d52 No revision has been approved for this page. It is currently under review by our subject matter experts. Jump to: navigation, search Loading... 1....

  16. Inverse magnetocaloric effect in Ce(Fe{sub 0.96}Ru{sub 0.04}){sub 2}: Effect of fast neutron irradiation

    SciTech Connect (OSTI)

    Dube, V.; Mishra, P. K.; Prajapat, C. L.; Singh, M. R.; Ravikumar, G.; Rajarajan, A. K.; Sastry, P. U.; Thakare, S. V.

    2013-02-05

    We have shown the effect of fast neutron irradiation on the magnetic phase transition and magnetocaloric effect (MCE) in a doped Ce(Fe{sub 0.96}Ru{sub 0.04}){sub 2}, intermettalic. We show that this leads to suppression of MCE and a to a disordered ferromagnetic phase.

  17. Mechanistic Insights of Ethanol Steam Reforming over NiCeO x (111): The Importance of Hydroxyl Groups for Suppressing Coke Formation

    SciTech Connect (OSTI)

    Liu, Zongyuan; Ducho?, Tom; Wang, Huanru; Peterson, Erik W.; Zhou, Yinghui; Luo, Si; Zhou, Jing; Matoln, Vladimir; Stacchiola, Dario J.; Rodriguez, Jos A.; Senanayake, Sanjaya D.

    2015-07-30

    We have studied the reaction of ethanol and water over NiCeO2-x(111) model surfaces to elucidate the mechanistic steps associated with the ethanol steam reforming (ESR) reaction. Our results provide insights about the importance of hydroxyl groups to the ESR reaction over Ni-based catalysts. Systematically, we have investigated the reaction of ethanol on NiCeO2-x(111) at varying Ce? concentrations (CeO1.82.0) with absence/presence of water using a combination of soft X-ray photoelectron spectroscopy (sXPS) and temperature-programmed desorption (TPD). Consistent with previous reports, upon annealing, metallic Ni formed on reduced ceria while NiO was the main component on fully oxidized ceria. Ni? is the active phase leading to both the CC and CH cleavage of ethanol but is also responsible for carbon accumulation or coking. We have identified a Ni?C phase that formed prior to the formation of coke. At temperatures above 600K, the lattice oxygen from ceria and the hydroxyl groups from water interact cooperatively in the removal of coke, likely through a strong metalsupport interaction between nickel and ceria that facilitates oxygen transfer.

  18. Mechanistic insights of ethanol steam reforming over Ni-CeOx(111): The importance of hydroxyl groups for suppressing coke formation

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Liu, Zongyuan; Senanayake, Sanjaya D.; Duchon, Tomas; Wang, Huanru; Peterson, Erik W.; Zhou, Yinghui; Luo, Si; Zhou, Jing; Matolin, Vladimir; Stacchiola, Dario J.; et al

    2015-07-10

    We have studied the reaction of ethanol and water over NiCeO2-x(111) model surfaces to elucidate the mechanistic steps associated with the ethanol steam reforming (ESR) reaction. Our results provide insights about the importance of hydroxyl groups to the ESR reaction over Ni-based catalysts. Systematically, we have investigated the reaction of ethanol on NiCeO2-x(111) at varying Ce? concentrations (CeO1.82.0) with absence/presence of water using a combination of soft X-ray photoelectron spectroscopy (sXPS) and temperature-programmed desorption (TPD). Consistent with previous reports, upon annealing, metallic Ni formed on reduced ceria while NiO was the main component on fully oxidized ceria. Ni? is themoreactive phase leading to both the CC and CH cleavage of ethanol but is also responsible for carbon accumulation or coking. We have identified a Ni?C phase that formed prior to the formation of coke. At temperatures above 600K, the lattice oxygen from ceria and the hydroxyl groups from water interact cooperatively in the removal of coke, likely through a strong metalsupport interaction between nickel and ceria that facilitates oxygen transfer.less

  19. Mechanistic Insights of Ethanol Steam Reforming over Ni–CeO x (111): The Importance of Hydroxyl Groups for Suppressing Coke Formation

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Liu, Zongyuan; Duchoň, Tomáš; Wang, Huanru; Peterson, Erik W.; Zhou, Yinghui; Luo, Si; Zhou, Jing; Matolín, Vladimir; Stacchiola, Dario J.; Rodriguez, José A.; et al

    2015-07-30

    We have studied the reaction of ethanol and water over Ni–CeO2-x(111) model surfaces to elucidate the mechanistic steps associated with the ethanol steam reforming (ESR) reaction. Our results provide insights about the importance of hydroxyl groups to the ESR reaction over Ni-based catalysts. Systematically, we have investigated the reaction of ethanol on Ni–CeO2-x(111) at varying Ce³⁺ concentrations (CeO1.8–2.0) with absence/presence of water using a combination of soft X-ray photoelectron spectroscopy (sXPS) and temperature-programmed desorption (TPD). Consistent with previous reports, upon annealing, metallic Ni formed on reduced ceria while NiO was the main component on fully oxidized ceria. Ni⁰ is themore » active phase leading to both the C–C and C–H cleavage of ethanol but is also responsible for carbon accumulation or coking. We have identified a Ni₃C phase that formed prior to the formation of coke. At temperatures above 600K, the lattice oxygen from ceria and the hydroxyl groups from water interact cooperatively in the removal of coke, likely through a strong metal–support interaction between nickel and ceria that facilitates oxygen transfer.« less

  20. Crystal Chemistry and Luminescence of Ce3+ -Doped Lu2CaMg2(Si,Ge)3O12 and Its Use in LED Based Lighting

    SciTech Connect (OSTI)

    Setlur,A.; Heward, W.; Gao, Y.; Srivastava, A.; Chandron, R.; Shankar, M.

    2006-01-01

    In this paper, we describe the formation and luminescence of a new garnet phosphor for light emitting diode (LED) based lighting, Lu{sub 2}CaMg{sub 2}(Si,Ge){sub 3}O{sub 12}:Ce{sup 3+}.The regions for garnet phase formation are initially described with respect to larger rare earth substitution and show reasonable correlation to previous crystal chemistry studies for the garnet parent structure. While the pure silicate phosphor also has apatite second phases, a significant amount of Ce{sup 3+} enters the garnet phase, giving Ce{sup 3+} luminescence that is significantly redder when compared to typical Al{sup 3+} garnet phosphors with quantum efficiencies comparable to commercial Ce{sup 3+} garnet phosphors. Potential reasons for the emission red shift and the high quantum efficiency are discussed. Finally, the performance of these new phosphors is tested within LED based lamps. Lamps using these phosphors can reach color temperatures required for general illumination lighting and also have comparable phosphor conversion efficiencies when compared to lamps using typical garnet phosphors.

  1. High Catalytic Activity of Au/CeOx/TiO2(110) Controlled by the Nature of the Mixed Metal Oxide at the Nanometer Level

    SciTech Connect (OSTI)

    Park, J.; Graciani, J; Evans, J; Stacchiola, D; Ma, S; Liu, P; Nambu, A; Sanz, J; Hrbek, J; et. al.

    2009-01-01

    Mixed-metal oxides play a very important role in many areas of chemistry, physics, materials science, and geochemistry. Recently, there has been a strong interest in understanding phenomena associated with the deposition of oxide nanoparticles on the surface of a second (host) oxide. Here, scanning tunneling microscopy, photoemission, and density-functional calculations are used to study the behavior of ceria nanoparticles deposited on a TiO2(110) surface. The titania substrate imposes nontypical coordination modes on the ceria nanoparticles. In the CeOx/TiO2(110) systems, the Ce cations adopt an structural geometry and an oxidation state (+3) that are quite different from those seen in bulk ceria or for ceria nanoparticles deposited on metal substrates. The increase in the stability of the Ce3+ oxidation state leads to an enhancement in the chemical and catalytic activity of the ceria nanoparticles. The codeposition of ceria and gold nanoparticles on a TiO2(110) substrate generates catalysts with an extremely high activity for the production of hydrogen through the water-gas shift reaction (H2O + CO ? H2 + CO2) or for the oxidation of carbon monoxide (2CO + O2 ? 2CO2). The enhanced stability of the Ce3+ state is an example of structural promotion in catalysis described here on the atomic level. The exploration of mixed-metal oxides at the nanometer level may open avenues for optimizing catalysts through stabilization of unconventional surface structures with special chemical activity.

  2. Electrical properties of dispersions of graphene in mineral oil

    SciTech Connect (OSTI)

    Monteiro, O. R.

    2014-02-03

    Dispersions of graphene in mineral oil have been prepared and electrical conductivity and permittivity have been measured. The direct current (DC) conductivity of the dispersions depends on the surface characteristics of the graphene platelets and followed a percolation model with a percolation threshold ranging from 0.05 to 0.1?wt. %. The difference in DC conductivities can be attributed to different states of aggregation of the graphene platelets and to the inter-particle electron transfer, which is affected by the surface radicals. The frequency-dependent conductivity (?(?)) and permittivity (?(?)) were also measured. The conductivity of dispersions with particle contents much greater than the percolation threshold remains constant and equal to the DC conductivity at low frequencies ? with and followed a power-law ?(?)???{sup s} dependence at very high frequencies with s?0.9. For dispersions with graphene concentration near the percolation threshold, a third regime was displayed at intermediate frequencies indicative of interfacial polarization consistent with Maxwell-Wagner effect typically observed in mixtures of two (or more) phases with very distinct electrical and dielectric properties.

  3. Geothermal Geodatabase for Wagon Wheel Hot Springs, Mineral County, Colorado

    SciTech Connect (OSTI)

    Zehner, Richard

    2012-11-01

    Geothermal Geodatabase for Wagon Wheel Hot Springs, Mineral County, Colorado By Richard Rick Zehner Geothermal Development Associates Reno Nevada USA 775.737.7806 rzehner@gdareno.com For Flint Geothermal LLC, Denver Colorado Part of DOE Grant EE0002828 2013 This is an ESRI geodatabase version 10, together with an ESRI MXD file version 10.2 Data is in UTM Zone 13 NAD27 projection North boundary: approximately 4,189,000 South boundary: approximately 4,170,000 West boundary: approximately 330,000 East boundary: approximately 351,000 This geodatabase was built to cover several geothermal targets developed by Flint Geothermal in 2012 during a search for high-temperature systems that could be exploited for electric power development. Several of the thermal springs at Wagon Wheel Gap have geochemistry and geothermometry values indicative of high-temperature systems. The datasets in the geodatabase are a mixture of public domain data as well as data collected by Flint Geothermal, now being made public. It is assumed that the user has internet access, for the mxd file accesses ESRIs GIS servers. Datasets include: 1. Results of reconnaissance shallow (2 meter) temperature surveys 2. Air photo lineaments 3. Groundwater geochemistry 4. Power lines 5. Georeferenced geologic map of Routt County 6. Various 1:24,000 scale topographic maps

  4. Investigation of the hydrothermal crystallisation of the perovskite solid solution NaCe{sub 1?x}La{sub x}Ti{sub 2}O{sub 6} and its defect chemistry

    SciTech Connect (OSTI)

    Harunsani, Mohammad H.; Woodward, David I.; Peel, Martin D.; Ashbrook, Sharon E.; Walton, Richard I.

    2013-11-15

    Perovskites of nominal composition NaCe{sub 1?x}La{sub x}Ti{sub 2}O{sub 6} (0?x?1) crystallise directly under hydrothermal conditions at 240 C. Raman spectroscopy shows distortion from the ideal cubic structure and Rietveld analysis of powder X-ray and neutron diffraction reveals that the materials represent a continuous series in rhombohedral space group R3-bar c. Ce L{sub III}-edge X-ray absorption near edge structure spectroscopy shows that while the majority of cerium is present as Ce{sup 3+} there is evidence for Ce{sup 4+}. The paramagnetic Ce{sup 3+} affects the chemical shift and line width of {sup 23}Na MAS NMR spectra, which also show with no evidence for A-site ordering. {sup 2}H MAS NMR of samples prepared in D{sub 2}O shows the inclusion of deuterium, which IR spectroscopy shows is most likely to be as D{sub 2}O. The deuterium content is highest for the cerium-rich materials, consistent with oxidation of some cerium to Ce{sup 4+} to provide charge balance of A-site water. - Graphical abstract: A multi-element A-site perovskite crystallises directly from aqueous, basic solutions at 240 C; while the paramagnetic effect of Ce{sup 3+} on the {sup 23}Na NMR shows a homogeneous solid-solution, the incorporation of A-site water is also found from {sup 2}H NMR and IR, with oxidation of some cerium to charge balance proved by XANES spectroscopy. Display Omitted - Highlights: Direct hydrothermal synthesis allows crystallisation of a perovskite solid-solution. XANES spectroscopy shows some oxidation of Ce{sup 3+} to Ce{sup 4+}. The paramagnetism of Ce{sup 3+} shifts and broadens the {sup 23}Na solid-state NMR. The perovskite materials incorporate water as an A-site defect.

  5. Utilization of coal associated minerals. Quarterly report No. 11, April 1-June 30, 1980

    SciTech Connect (OSTI)

    Slonaker, J. F.; Akers, D. J.; Alderman, J. K.

    1980-08-29

    The purpose of this research program is to examine the effects of coal mineral materials on coal waste by-product utilization and to investigate new and improved methods for the utilization of waste by-products from cleaning, combustion and conversion processing of coal. The intermediate objectives include: (1) the examination of the effects of cleaning, gasification and combustion on coal mineral materials; and (2) the changes which occur in the coal wastes as a result of both form and distribution of mineral materials in feed coals in conjunction with the coal treatment effects resulting from coal cleaning or either gasification or combustion.

  6. Micro-Analysis of Actinide Minerals for Nuclear Forensics and Treaty Verification

    SciTech Connect (OSTI)

    M. Morey, M. Manard, R. Russo, G. Havrilla

    2012-03-22

    Micro-Raman spectroscopy has been demonstrated to be a viable tool for nondestructive determination of the crystal phase of relevant minerals. Collecting spectra on particles down to 5 microns in size was completed. Some minerals studied were weak scatterers and were better studied with the other techniques. A decent graphical software package should easily be able to compare collected spectra to a spectral library as well as subtract out matrix vibration peaks. Due to the success and unequivocal determination of the most common mineral false positive (zircon), it is clear that Raman has a future for complementary, rapid determination of unknown particulate samples containing actinides.

  7. Substitution effect on the magnetic and transport properties of CeNi{sub 0.8−x}Mn{sub x}Bi{sub 2}

    SciTech Connect (OSTI)

    Kim, Soo-Whan; Lee, Kyujoon; Jung, Myung-Hwa; Adroja, D. T.; Demmel, F.; Taylor, J. W.

    2014-08-21

    We report the results of Mn substitution for Ni in CeNi{sub 0.8}Bi{sub 2} (i.e., CeNi{sub 0.8−x}Mn{sub x}Bi{sub 2}). All the samples have an antiferromagnetic ordered state below T{sub N} = 5.0 K due to localized 4f-magnetic moment on the Ce ions. Besides this antiferromagnetic ordering caused by Ce, the magnetic and transport properties are abruptly changed with increasing Mn contents at the boundary composition of x = 0.4. The magnetic state is changed into a ferromagnetic state around 200 K for x > 0.4, where the electrical resistivity is strongly suppressed to become simple metallic. These results of ferromagnetism and metallicity can be explained by the double exchange mechanism, rather than the simple picture of Doniach phase diagram. The mixed valence states of Ni and Mn ions are confirmed by X-ray photoelectron spectroscopy. For x ≤ 0.4, the initial Ni{sup 3+} state gradually changes to the Ni{sup 2+} state with increasing x up to 0.4. On further increase of x > 0.4, the Ni{sup 2+} state is replaced by the Mn{sup 2+} state, which gradually changes to the final Mn{sup 3+} state. We also present an inelastic neutron scattering (INS) measurements on CeNi{sub 0.8}Bi{sub 2} (i.e., x = 0) between 1.2 and 12 K. The high energy INS study reveals the presence of two well-defined crystal electric field (CEF) excitations near 9 meV and 19 meV at 1.2 K and 6 K, while the low energy INS study reveals the presence of quasielastic scattering above 4 K. We will discuss our INS results of CeNi{sub 0.8}Bi{sub 2} based on the CEF model.

  8. Multivariate statistical analysis of stream sediments for mineral resources from the Craig NTMS Quadrangle, Colorado

    SciTech Connect (OSTI)

    Beyth, M.; McInteer, C.; Broxton, D.E.; Bolivar, S.L.; Luke, M.E.

    1980-06-01

    Multivariate statistical analyses were carried out on Hydrogeochemical and Stream Sediment Reconnaissance data from the Craig quadrangle, Colorado, to support the National Uranium Resource Evaluation and to evaluate strategic or other important commercial mineral resources. A few areas for favorable uranium mineralization are suggested for parts of the Wyoming Basin, Park Range, and Gore Range. Six potential source rocks for uranium are postulated based on factor score mapping. Vanadium in stream sediments is suggested as a pathfinder for carnotite-type mineralization. A probable northwest trend of lead-zinc-copper mineralization associated with Tertiary intrusions is suggested. A few locations are mapped where copper is associated with cobalt. Concentrations of placer sands containing rare earth elements, probably of commercial value, are indicated for parts of the Sand Wash Basin.

  9. H.R.S. 182-6 - Mineral Exploration | Open Energy Information

    Open Energy Info (EERE)

    search OpenEI Reference LibraryAdd to library Legal Document- StatuteStatute: H.R.S. 182-6 - Mineral ExplorationLegal Published NA Year Signed or Took Effect 2012 Legal...

  10. Cal. PRC Section 6910 - Oil and Gas and Mineral Leases | Open...

    Open Energy Info (EERE)

    PRC Section 6910 - Oil and Gas and Mineral Leases Jump to: navigation, search OpenEI Reference LibraryAdd to library Legal Document- StatuteStatute: Cal. PRC Section 6910 - Oil and...

  11. Cal. PRC Section 6909 - Oil and Gas and Mineral Leases: Geothermal...

    Open Energy Info (EERE)

    09 - Oil and Gas and Mineral Leases: Geothermal Resources Jump to: navigation, search OpenEI Reference LibraryAdd to library Legal Document- StatuteStatute: Cal. PRC Section 6909 -...

  12. Title 25 CFR 225 Oil and Gas, Geothermal, and Solid Minerals...

    Open Energy Info (EERE)

    5 Oil and Gas, Geothermal, and Solid Minerals Agreements Jump to: navigation, search OpenEI Reference LibraryAdd to library Legal Document- Federal RegulationFederal Regulation:...

  13. Diffraction Studies from Minerals to Organics - Lessons Learned from Materials Analyses

    SciTech Connect (OSTI)

    Whitfield, Pamela S

    2014-01-01

    In many regards the study of materials and minerals by powder diffraction techniques are complimentary, with techniques honed in one field equally applicable to the other. As a long-time materials researcher many of the examples are of techniques developed for materials analysis applied to minerals. However in a couple of cases the study of new minerals was the initiation into techniques later used in materials-based studies. Hopefully they will show that the study of new minerals structures can provide opportunities to add new methodologies and approaches to future problems. In keeping with the AXAA many of the examples have an Australian connection, the materials ranging from organics to battery materials.

  14. Application Of Fluid Inclusion And Rock-Gas Analysis In Mineral...

    Open Energy Info (EERE)

    to analyze these gases in fluid inclusions in jasperoid around the Pueblo Viejo gold-silver deposit, in vein minerals from the Creede silver-lead-zinc deposit, and from...

  15. Analysis of Mineral Trapping for CO2 Disposal in Deep Aquifers

    Office of Scientific and Technical Information (OSTI)

    ... The deepest aquifers in the United States usually contain ... Mineral Society of America, v. 31, p. 291-351, ... D.K., 1978, Summary and critique of the thermodynamic ...

  16. Revenue ruling 73-538: the service's assault on percentage depletion for ''D'' miners

    SciTech Connect (OSTI)

    Barnes, D.A.

    1983-01-01

    In this article, the author examines the Internal Revenue Service's ruling that storage and loading for shipment at the mine site are nonmining processes for ores and minerals described in section 613(c)(4)(D) of the Internal Revenue Code. He explains the tax consequences of the ruling and discusses the correctness of the position taken by the Internal Revenue Service in light of the relevant case law and the language and legislative history of the statute. The effect of the ruling is to reduce the percentage depletion deduction available to many miners of ores and minerals described in section 613(c)(4)(D), including miners of lead, zinc, copper, gold, silver, uranium, fluorspar, potash, soda ash, garnet and tungsten. (JMT)

  17. Discovery of bridgmanite, the most abundant mineral in Earth, in a shocked

    Office of Scientific and Technical Information (OSTI)

    meteorite (Journal Article) | SciTech Connect SciTech Connect Search Results Journal Article: Discovery of bridgmanite, the most abundant mineral in Earth, in a shocked meteorite Citation Details In-Document Search Title: Discovery of bridgmanite, the most abundant mineral in Earth, in a shocked meteorite Authors: Tschauner, Oliver ; Ma, Chi ; Beckett, John R. ; Prescher, Clemens ; Prakapenka, Vitali B. ; Rossman, George R. [1] ; UNLV) [2] ; CIT) [2] + Show Author Affiliations (UC) (

  18. Microbial and Chemical Enhancement of In-Situ Carbon Mineralization in

    Office of Scientific and Technical Information (OSTI)

    Geological Formation (Technical Report) | SciTech Connect Microbial and Chemical Enhancement of In-Situ Carbon Mineralization in Geological Formation Citation Details In-Document Search Title: Microbial and Chemical Enhancement of In-Situ Carbon Mineralization in Geological Formation × You are accessing a document from the Department of Energy's (DOE) SciTech Connect. This site is a product of DOE's Office of Scientific and Technical Information (OSTI) and is provided as a public service.

  19. FLUIDIZED BED STEAM REFORMED MINERAL WASTE FORMS: CHARACTERIZATION AND DURABILITY TESTING

    SciTech Connect (OSTI)

    Jantzen, C; Troy Lorier, T; John Pareizs, J; James Marra, J

    2006-12-06

    Fluidized Bed Steam Reforming (FBSR) is being considered as a potential technology for the immobilization of a wide variety of high sodium low activity wastes (LAW) such as those existing at the Hanford site, at the Idaho National Laboratory (INL), and the Savannah River Site (SRS). The addition of clay, charcoal, and a catalyst as co-reactants with the waste denitrates the aqueous wastes and forms a granular mineral waste form that can subsequently be made into a monolith for disposal if necessary. The waste form produced is a multiphase mineral assemblage of Na-Al-Si (NAS) feldspathoid minerals with cage and ring structures and iron bearing spinel minerals. The mineralization occurs at moderate temperatures between 650-750 C in the presence of superheated steam. The cage and ring structured feldspathoid minerals atomically bond radionuclides like Tc-99 and Cs-137 and anions such as SO{sub 4}, I, F, and Cl. The spinel minerals stabilize Resource Conservation and Recovery Act (RCRA) hazardous species such as Cr and Ni. Granular mineral waste forms were made from (1) a basic Hanford Envelope A low activity waste (LAW) simulant and (2) an acidic INL simulant commonly referred to as sodium bearing waste (SBW) in pilot scale facilities at the Science Applications International Corporation (SAIC) Science and Technology Applications Research (STAR) facility in Idaho Falls, ID. The FBSR waste forms were characterized and the durability tested via ASTM C1285 (Product Consistency Test), the Environmental Protection Agency (EPA) Toxic Characteristic Leaching Procedure (TCLP), and the Single Pass Flow Through (SPFT) test. The results of the SPFT testing and the activation energies for dissolution are discussed in this study.

  20. FLUIDIZED BED STEAM REFORMED MINERAL WASTE FORMS: CHARACTERIZATION AND DURABILITY TESTING

    SciTech Connect (OSTI)

    Jantzen, C; Troy Lorier, T; John Pareizs, J; James Marra, J

    2007-03-31

    Fluidized Bed Steam Reforming (FBSR) is being considered as a potential technology for the immobilization of a wide variety of high sodium low activity wastes (LAW) such as those existing at the Hanford site, at the Idaho National Laboratory (INL), and the Savannah River Site (SRS). The addition of clay, charcoal, and a catalyst as co-reactants with the waste denitrates the aqueous wastes and forms a granular mineral waste form that can subsequently be made into a monolith for disposal if necessary. The waste form produced is a multiphase mineral assemblage of Na-Al-Si (NAS) feldspathoid minerals with cage and ring structures and iron bearing spinel minerals. The mineralization occurs at moderate temperatures between 650-750 C in the presence of superheated steam. The cage and ring structured feldspathoid minerals atomically bond radionuclides like Tc-99 and Cs-137 and anions such as SO4, I, F, and Cl. The spinel minerals stabilize Resource Conservation and Recovery Act (RCRA) hazardous species such as Cr and Ni. Granular mineral waste forms were made from (1) a basic Hanford Envelope A low-activity waste (LAW) simulant and (2) an acidic INL simulant commonly referred to as sodium bearing waste (SBW) in pilot scale facilities at the Science Applications International Corporation (SAIC) Science and Technology Applications Research (STAR) facility in Idaho Falls, ID. The FBSR waste forms were characterized and the durability tested via ASTM C1285 (Product Consistency Test), the Environmental Protection Agency (EPA) Toxic Characteristic Leaching Procedure (TCLP), and the Single Pass Flow Through (SPFT) test. The results of the SPFT testing and the activation energies for dissolution are discussed in this study.

  1. Low temperature specific heat of the Kondo-semimetal CeNiSn in zero and applied magnetic fields

    SciTech Connect (OSTI)

    Brueckl, A.; Neumaier, K.; Einzel, D.; Andres, K.; Flaschin, S.; Kalvius, G.M.; Nakamoto, G.; Takabatake, T.

    1999-06-01

    The specific heat of several CeNiSn single crystals of various purity has been measured in the temperature range from 25 mK to 5 K and in magnetic fields from zero to 7 Tesla. At very low temperatures (below {approximately} 200 mK) the specific heat is found to vary linearly with temperature (C = {gamma}T), the coefficient {gamma} decreasing with increasing purity. Above 200 mK, the specific heat is well described as the sum of a linear and a quadratic term. An applied magnetic field affects mostly the linear term, which first slightly decreases, then strongly increases with field. In magnetic fields, a nuclear hyperfine specific heat contribution is superimposed, which is due mostly to the bare Zeeman-splitting of the {sup 115}Sn, {sup 117}Sn, {sup 119}Sn nuclei (all with spin I = 1/2 and with abundances of 0.35, 7.61, and 8.58% respectively) in the externally applied field. The results on the specific heat at very low temperatures in applied fields fit into the model of an enhanced (heavy-fermion type) density of states which is modified by coherent antiferromagnetic fluctuations into a V-shaped density of states at the Fermi energy.

  2. Electrochemical Study on the Electrodeposition of U, Nd, Ce, La and Y on a Liquid Cadmium Cathode in a LiCl-KCl Eutectic Salt

    SciTech Connect (OSTI)

    Sung Bin Park; Jong Hyeon Lee; Sung Chan Hwang; Young Ho Kang; Joon Bo Shim; Han Soo Lee; Eung Ho Kim; Seong Won Park

    2007-07-01

    Electro-depositions of U, Nd, Ce, La and Y on a liquid cadmium cathode in a LiCl-KCl eutectic salt were studied by using an electrolytic cell. For the LiCl-KCl-UCl{sub 3}- NdCl{sub 3}-CeCl{sub 3}-LaCl{sub 3}-YCl{sub 3}/Cd system, cyclic voltammograms and polarization curves were measured and the electrochemical properties of the system were discussed. From the results of the electro-depositions of U and rare earth metals on the LCC, separation factors and recovery ratios of U and REs were obtained and co-electro-depositions of U and REs were investigated. (authors)

  3. Lu.sub.1-xI.sub.3:Ce.sub.x--a scintillator for gamma ray spectroscopy and time-of-flight PET

    DOE Patents [OSTI]

    Shah, Kanai S.

    2007-02-06

    The present invention concerns very fast scintillator materials comprising lutetium iodide doped with Cerium (Lu.sub.1-xI.sub.3:Ce.sub.x; LuI.sub.3:Ce). The LuI.sub.3 scintillator material has surprisingly good characteristics including high light output, high gamma ray stopping efficiency, fast response, low cost, good proportionality, and minimal afterglow that the material is useful for gamma ray spectroscopy, medical imaging, nuclear and high energy physics research, diffraction, non-destructive testing, nuclear treaty verification and safeguards, and geological exploration. The timing resolution of the scintillators of the present invention provide compositions capable of resolving the position of an annihilation event within a portion of a human body cross-section.

  4. Nodal to nodeless superconducting energy gap structure change concomitant with Fermi surface reconstruction in the heavy-fermion CeCoIn?

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Kim, Hyunsoo; Petrovic, C.; Tanatar, M. A.; Flint, R.; Hu, Rongwei; White, B. D.; Lum, I. K.; Maple, M. B.; Prozorov, R.

    2015-01-15

    The London penetration depth ?(T) was measured in single crystals of Ce1xRxCoIn?, R=La, Nd, and Yb down to Tmin ? 50 mK (Tc/Tmin ~50) using a tunnel-diode resonator. In the cleanest samples ??(T) is best described by the power law, ??(T) ? Tn, with n ~ 1, consistent with line nodes. Substitutions of Ce with La, Nd, and Yb lead to similar monotonic suppressions of Tc, however, the effects on ??(T) differ. While La and Nd dopings lead to increase of the exponent n and saturation at n ~ 2, as expected for a dirty nodal superconductor, Yb doping leadsmoreto n > 3, suggesting a change from nodal to nodeless superconductivity. This superconducting gap structure change happens in the same doping range where changes of the Fermi surface topology were reported, implying that the nodal structure and Fermi surface topology are closely linked.less

  5. Commissioning of the 112 MHz SRF Gun and 500 MHz bunching cavities for the CeC PoP Linac

    SciTech Connect (OSTI)

    Belomestnykh, S.; Ben-Zvi, I.; Brutus, J. C.; Litvinenko, V.; McIntosh, P.; Moss, A.; Narayan, G.; Orfin, P.; Pinayev, I.; Rao, T.; Skaritka, J.; Smith, K.; Than, R.; Tuozzolo, J.; Wang, E.; Wheelhouse, A.; Wu, Q.; Xiao, B.; Xin, T.; Xu, W.; Zaltsman, A.

    2015-05-03

    The Coherent electron Cooling Proof-of-Principle (CeC PoP) experiment at BNL includes a short electron linac. During Phase 1, a 112 MHz superconducting RF photo-emission gun and two 500 MHz normal conducting bunching cavities were installed and are under commissioning. The paper describes the Phase1 linac layout and presents commissioning results for the cavities and associated RF, cryogenic and other sub-systems

  6. High Activity of Ce1-xNixO2-y for H2 Production through Ethanol Steam Reforming: Tuning Catalytic Performance through Metal-Oxide Interactions

    SciTech Connect (OSTI)

    G Zhou; L Barrio; S Agnoli; S Senanayake; J Evans; A Kubacka; M Estrella; J Hanson; A Martinez-Arias; et al.

    2011-12-31

    The importance of the oxide: Ce{sub 0.8}Ni{sub 0.2}O{sub 2-y} is an excellent catalyst for ethanol steam reforming. Metal-oxide interactions perturb the electronic properties of the small particles of metallic nickel present in the catalyst under the reaction conditions and thus suppress any methanation activity. The nickel embedded in ceria induces the formation of O vacancies, which facilitate cleavage of the OH bonds in ethanol and water.

  7. Remarkably robust and correlated coherence and antiferromagnetism in (Ce1-xLax)Cu2Ge2

    SciTech Connect (OSTI)

    Hodovanets, H.; Budko, S. L.; Straszheim, W. E.; Taufour, V.; Mun, E. D.; Kim, H.; Flint, R.; Canfield, P. C.

    2015-06-08

    We present magnetic susceptibility, resistivity, specific heat, and thermoelectric power measurements on (Ce1-xLax)Cu2Ge2 single crystals (0 ? x ? 1). With La-substitution, the antiferromagnetic temperature TN is suppressed in an almost linear fashion and moves below 0.36 K, the base temperature of our measurements for x > 0.8. Surprisingly, in addition to robust antiferromagnetism, the system also shows low temperature coherent scattering below Tcoh up to ~0.9 of La, indicating a small percolation limit ~9% of Ce. Tcoh as a function of magnetic field was found to have different behavior for x < 0.9 and x > 0.9. Remarkably, (Tcoh)2 at H = 0 was found to be linearly proportional to TN. In conclusion, the jump in the magnetic specific heat ?Cm at TN as a function of TK/TN for (Ce1-xLax)Cu2Ge2 follows the theoretical prediction based on the molecular field calculation for the S = 1/2 resonant level model.

  8. Spin-glass freezing above the ordering temperature for the Kondo ferromagnet CeNi{sub 0.4}Cu{sub 0.6}

    SciTech Connect (OSTI)

    Gomez Sal, J.C.; Garcia Soldevilla, J.; Blanco, J.A.; Espeso, J.I.; Rodriguez Fernandez, J.; Luis, F.; Bartolome, F.; Bartolome, J.

    1997-11-01

    The low-temperature magnetic and transport properties of the orthorhombic CeNi{sub 0.4}Cu{sub 0.6} compound have been determined from the analysis of specific heat, ac magnetic susceptibility, electrical resistivity, elastic and inelastic neutron scattering. These measurements present intriguing experimental results that could not be explained within the usual phenomenology of Ce-based compounds. C{sub p} and {chi}{sub ac} present anomalies around 1 K corresponding to ferromagnetic order as confirmed by neutron diffraction. The magnetic structure is collinear with very reduced moments, 0.6{mu}{sub B}/Ce lying in the b direction. Additionally, a clear Kondo behavior is observed with a Kondo temperature T{sub K}=1.9K estimated from quasielastic neutron scattering. Above the ordering temperature, further anomalies are observed in C{sub p} and {chi}{sub ac} that could not be explained as originating from crystal electric field or Kondo effects. From the frequency and field dependence of the {chi}{sub ac}, above T{sub c}, a spin-glass state with a freezing temperature T{sub f}=2K is proposed for this compound. This unusual magnetic behavior is discussed in terms of mixed (positive and negative) Ruderman-Kittel-Kasuya-Yosida interactions, randomness (structural disorder), large hybridization (Kondo effect), and strong magnetocrystalline anisotropy (crystal electric field effects). {copyright} {ital 1997} {ital The American Physical Society}

  9. Electronic structure of the heavy-fermion caged compound Ce3Pd20X6(X=Si,Ge) studied by density functional theory and photoelectron spectroscopy

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Yamaoka, Hitoshi; Schwier, Eike F.; Arita, Masashi; Shimada, Kenya; Tsujii, Naohito; Jarrige, Ignace; Jiang, Jian; Hayashi, Hirokazu; Iwasawa, Hideaki; Namatame, Hirofumi; et al

    2015-03-30

    The electronic structure of Ce₃Pd₂₀X₆ (X = Si, Ge) has been studied using detailed density functional theory (DFT) calculations and high-resolution photoelectron spectroscopy (PES) measurements. The orbital decomposition of the electronic structure by DFT calculations indicates that Ce atoms at the (8c) site surrounded by 16 Pd atoms have a more localized nature and a tendency to be magnetic. Ce atoms in the (4a) site surrounded by 12 Pd and 6 X atoms, on the other, show only a negligible magnetic moment. In the photoemission valence-band spectra we observe a strong f⁰ (Ce⁴⁺) component with a small fraction of f¹more »(Ce³⁺) component. The spectral weight of f¹ component near the Fermi level Ce₃Pd₂₀Si₆ is stronger than that for Ce₃Pd₂₀Ge₆ at the 4d-4f resonance, suggesting stronger c-f hybridization in the former. This may hint to the origin of the large electronic specific coefficient of Ce₃Pd₂₀Si₆ compared to Ce₃Pd₂₀Ge₆.« less

  10. Magnetic order and heavy fermion behavior in CePd{sub 1+x}Al{sub 6-x}: Synthesis, structure, and physical properties

    SciTech Connect (OSTI)

    Tobash, Paul H., E-mail: ptobash@lanl.go [Materials Physics and Application Division, MPA-10, Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Department of Chemistry and Biochemistry, University of Delaware, Newark, DE 19716 (United States); Ronning, Filip; Thompson, J.D. [Materials Physics and Application Division, MPA-10, Los Alamos National Laboratory, Los Alamos, NM 87545 (United States); Bobev, Svilen [Department of Chemistry and Biochemistry, University of Delaware, Newark, DE 19716 (United States); Bauer, Eric D. [Materials Physics and Application Division, MPA-10, Los Alamos National Laboratory, Los Alamos, NM 87545 (United States)

    2010-03-15

    The physical properties including magnetic susceptibility, specific heat, and electrical resistivity of single crystals are reported for the compound CePd{sub 1+x}Al{sub 6-x} (x=0.5) which crystallizes in the tetragonal SrAu{sub 2}Ga{sub 5}-type structure (space group P4/mmm). The compound was grown from an excess of molten Al flux from the respective elements and the crystal structure was established from single-crystal X-ray diffraction. Anomalies in the low temperature specific heat C{sub p}(T) and electrical resistivity rho(T) show that the compound undergoes ferromagnetic order at T{sub C}=2.8 K. In the ordered state, CePd{sub 1.5}Al{sub 5.5} displays heavy fermion behavior with a Sommerfeld coefficient of ca. 500 mJ/mol-K{sup 2}. - Graphical abstract: The compound CePd{sub 1+x}Al{sub 6-x} (x=0.5) has been synthesized and structurally characterized by single-crystal X-ray diffraction. The measured physical properties of temperature and field dependent magnetic susceptibility, specific heat, and electrical resistivity suggests that the compound undergoes ferromagnetic order at ca. 2.8 K and further exhibits relatively heavy fermion behavior with a Sommerfeld coefficient of 500 mJ/mol-K2.

  11. Resolution of the discrepancy between the variation of the physical properties of Ce1-xYbxCoIn5 single crystals and thin films with Yb composition

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Jang, S.; White, B. D.; Lum, I. K.; Kim, H.; Tanatar, M. A.; Straszheim, W. E.; Prozorov, R.; Keiber, T.; Bridges, F.; Shu, L.; et al

    2014-11-18

    The extraordinary electronic phenomena including an Yb valence transition, a change in Fermi surface topology, and suppression of the heavy fermion quantum critical field at a nominal concentration x≈0.2 have been found in the Ce1-xYbxCoIn5 system. These phenomena have no discernable effect on the unconventional superconductivity and normal-state non-Fermi liquid behaviour that occur over a broad range of x up to ~0.8. However, the variation of the coherence temperature T* and the superconducting critical temperature Tc with nominal Yb concentration x for bulk single crystals is much weaker than that of thin films. To determine whether differences in the actualmore » Yb concentration of bulk single crystals and thin film samples might be responsible for these discrepancies, we employed Vegard’s law and the spectroscopically determined values of the valences of Ce and Yb as a function of x to determine the actual composition xact of bulk single crystals. This analysis is supported by energy-dispersive X-ray spectroscopy, wavelength-dispersive X-ray spectroscopy, and transmission X-ray absorption edge spectroscopy measurements. The actual composition xact is found to be about one-third of the nominal concentration x up to x~0.5, and resolves the discrepancy between the variation of the physical properties of Ce1-xYbxCoIn5 single crystals and thin films with Yb concentration.« less

  12. The rare earth silicon phosphides LnSi{sub 2}P{sub 6} (Ln = La, Ce, Pr, and Nd)

    SciTech Connect (OSTI)

    Kaiser, P.; Jeitschko, W.

    1996-07-01

    The title compounds were prepared in well-crystallized form from a tin flux and their crystal structure was determined from single-crystal diffractometer data of LaSi{sub 2}P{sub 6}: Cmc2{sub 1}, a = 1012.9(3) pm, b = 2817.5(7) pm, c = 1037.4(5) pm, Z = 16, R = 0.034 for 3303 structure factors and 181 variable parameters. The structure of the isotypic compound CeSi{sub 2}P{sub 6} was also refined from single-crystal X-ray data: a = 1011.8(4) pm, b = 2803.1(8) pm, c = 1031.1(4) pm, R = 0.035 for 2132 F values and 181 variables. The silicon and the phosphorus atoms could be distinguished by comparing their occupancy parameters obtained from both structure refinements. The assignments agree with those deduced by structure-chemical arguments. These atoms form a three-dimensionally infinite framework polyanion, which accommodates four different kinds of rare earth atoms: three with nine and one with ten phosphorus neighbors. The silicon atoms are all in tetrahedral phosphorus coordination. There are phosphorus atoms which have only two rare earth and two silicon neighbors, but most phosphorus atoms have--in addition to the rare earth and silicon atoms--phosphorus neighbors, thus forming P{sub 3}, P{sub 4}, P{sub 5}, and P{sub 6} units. Using oxidation numbers, the compounds can be rationalized with the formulas Ln{sup 3+}(Si{sub 2}P{sub 6}){sub 3-} and Ln{sup 3+}(Si{sup 4+}){sub 2}(P{sub 6}){sup 11-}, where the octet rule is obeyed for the silicon and phosphorus atoms and two electrons are counted for each Si-P and P-P interaction.

  13. Antiferromagnetic Kondo lattice in the layered compound CePd1xBi? and comparison to the superconductor LaPd1xBi?

    SciTech Connect (OSTI)

    Han, Fei; Wan, Xiangang; Phelan, Daniel; Stoumpos, Constantinos C.; Sturza, Mihai; Malliakas, Christos D.; Li, Qing'an; Han, Tian-Heng; Zhao, Qingbiao; Chung, Duck Young; Kanatzidis, Mercouri G.

    2015-07-13

    The layered compound CePd1xBi? with the tetragonal ZrCuSi?-type structure was obtained from excess Bi flux. Magnetic susceptibility data of CePd1xBi? show an antiferromagnetic ordering below 6 K and are anisotropic along the c axis and the ab plane. The anisotropy is attributed to crystal-electric-field (CEF) effects and a CEF model which is able to describe the susceptibility data is given. An enhanced Sommerfeld coefficient ? of 0.191 J mol Ce? K? obtained from specific-heat measurement suggests a moderate Kondo effect in CePd1xBi?. Other than the antiferromagnetic peak at 6 K, the resistivity curve shows a shoulderlike behavior around 75 K which could be attributed to the interplay between Kondo and CEF effects. Magnetoresistance and Hall-effect measurements suggest that the interplay reconstructs the Fermi-surface topology of CePd1xBi? around 75 K. Electronic structure calculations reveal that the Pd vacancies are important to the magnetic structure and enhance the CEF effects which quench the orbital moment of Ce at low temperatures.

  14. Magnetic properties of bulk, and rapidly solidified nanostructured (Nd1-xCex)2Fe14-yCoyB ribbons

    SciTech Connect (OSTI)

    Pathak, Arjun K.; Khan, M.; Gschneidner, Jr., K. A.; McCallum, R. W.; Zhou, L.; Sun, K.; Kramer, M. J.; Pecharsky, V. K.

    2015-11-06

    Magnetic properties of Ce and Co co-doped (Nd1-xCex)2Fe14-yCoyB compounds have been investigated both in bulk polycrystalline and rapidly solidified nanostructured ribbon forms. For certain Ce concentrations the materials exhibit spin re-orientation transitions below 140 K. The Curie temperatures, saturation magnetizations, and other magnetic properties relevant for applications as permanent magnets are controlled by Ce and Co substitutions for Nd and Fe, respectively. Most importantly, the results show that Ce, Co co-doped compounds are excellent replacements for several Dy-based high performance permanent magnets (dysprosium is one of the critical elements and is, therefore, in short supply). As a result, the high temperature (>375 K) magnetic properties for Nd–Ce–Fe–Co–B based alloys show promise not only as a replacement for Dy-doped Nd2Fe14B permanent magnets, but the new alloys also require significantly lower amounts of Nd, which too is the critical element that can be replaced by a more abundant Ce.

  15. Mineral Dissolution and Secondary Precipitation on Quartz Sand in Simulated Hanford Tank Solutions Affecting Subsurface Porosity

    SciTech Connect (OSTI)

    Wang, Guohui; Um, Wooyong

    2012-11-23

    Highly alkaline nuclear waste solutions have been released from underground nuclear waste storage tanks and pipelines into the vadose zone at the U.S. Department of Energys Hanford Site in Washington, causing mineral dissolution and re-precipitation upon contact with subsurface sediments. High pH caustic NaNO3 solutions with and without dissolved Al were reacted with quartz sand through flow-through columns stepwise at 45, 51, and 89C to simulate possible reactions between leaked nuclear waste solution and primary subsurface mineral. Upon reaction, Si was released from the dissolution of quartz sand, and nitrate-cancrinite [Na8Si6Al6O24(NO3)2] precipitated on the quartz surface as a secondary mineral phase. Both steady-state dissolution and precipitation kinetics were quantified, and quartz dissolution apparent activation energy was determined. Mineral alteration through dissolution and precipitation processes results in pore volume and structure changes in the subsurface porous media. In this study, the column porosity increased up to 40.3% in the pure dissolution column when no dissolved Al was present in the leachate, whereas up to a 26.5% porosity decrease was found in columns where both dissolution and precipitation were observed because of the presence of Al in the input solution. The porosity change was also confirmed by calculation using the dissolution and precipitation rates and mineral volume changes.

  16. Process for removal of mineral particulates from coal-derived liquids

    DOE Patents [OSTI]

    McDowell, William J. (Knoxville, TN)

    1980-01-01

    Suspended mineral solids are separated from a coal-derived liquid containing the solids by a process comprising the steps of: (a) contacting said coal-derived liquid containing solids with a molten additive having a melting point of 100.degree.-500.degree. C. in an amount of up to 50 wt. % with respect to said coal-derived liquid containing solids, said solids present in an amount effective to increase the particle size of said mineral solids and comprising material or mixtures of material selected from the group of alkali metal hydroxides and inorganic salts having antimony, tin, lithium, sodium, potassium, magnesium, calcium, beryllium, aluminum, zinc, molybdenum, cobalt, nickel, ruthenium, rhodium or iron cations and chloride, iodide, bromide, sulfate, phosphate, borate, carbonate, sulfite, or silicate anions; and (b) maintaining said coal-derived liquid in contact with said molten additive for sufficient time to permit said mineral matter to agglomerate, thereby increasing the mean particle size of said mineral solids; and (c) recovering a coal-derived liquid product having reduced mineral solids content. The process can be carried out with less than 5 wt. % additive and in the absence of hydrogen pressure.

  17. Role of Ce4+ in the scintillation mechanism of codoped Gd3Ga3Al2O12:Ce

    SciTech Connect (OSTI)

    Wu, Yuntao; Meng, Fang; Li, Qi; Koschan, Merry; Melcher, Charles L.

    2014-10-17

    To control the time-response performance of widely used cerium-activated scintillators in cutting-edge medical-imaging devices, such as time-of-flight positron-emission tomography, a comprehensive understanding of the role of Ce valence states, especially stable Ce4+, in the scintillation mechanism is essential. However, despite some progress made recently, an understanding of the physical processes involving Ce4+ is still lacking. The aim of this work is to clarify the role of Ce4+ in scintillators by studying Ca2+ codoped Gd3Ga3Al2O12?Ce?(GGAG?Ce). By using a combination of optical absorption spectra and x-ray absorption near-edge spectroscopies, the correlation between Ca2+codoping content and the Ce4+ fraction is seen. The energy-level diagrams of Ce3+ and Ce4+ in the Gd3Ga3Al2O12 host are established by using theoretical and experimental methods, which indicate a higher position of the 5d1 state of Ce4+ in the forbidden gap in comparison to that of Ce3+. Underlying reasons for the decay-time acceleration resulting from Ca2+ codoping are revealed, and the physical processes of the Ce4+-emission model are proposed and further demonstrated by temperature-dependent radioluminescence spectra under x-ray excitation.

  18. Licensees and economic interest in minerals after Swank and revenue ruling 83-160

    SciTech Connect (OSTI)

    McMahon, M.J. Jr.

    1983-01-01

    In the three years since the Supreme Court decided in United States v. Swank that a coal operator mining a coal deposit under a written lease terminable without cause on 30 days notice held an economic interest in the mineral in place, tax literature began noting that this decision rejected a long-held position of the Internal Revenue Service (IRS). The author assesses the impact of Revenue Ruling 83-88, in which the IRS went beyond Swank in concluding that there is no minimum period during which a lessee must have a legal right to extract minerals as a prerequisite to an economic interest. He examines the proposition that, after Swank and Revenue Ruling 83-160, licensees who previously were considered not to have acquired an economic interest, should now be found to have an economic interest in the mineral deposit they are extracting.

  19. Hierarchical Heterogeneity at the CeO x TiO 2 Interface: Electronic and Geometric Structural Influence on the Photocatalytic Activity of Oxide on Oxide Nanostructures

    SciTech Connect (OSTI)

    Luo, Si; Nguyen-Phan, Thuy-Duong; Johnston-Peck, Aaron C.; Barrio, Laura; Sallis, Shawn; Arena, Dario A.; Kundu, Shankhamala; Xu, Wenqian; Piper, Louis F. J.; Stach, Eric A.; Polyanskiy, Dmitry E.; Fujita, Etsuko; Rodriguez, Jos A.; Senanayake, Sanjaya D.

    2015-01-13

    Mixed oxide interfaces are critical for delivering active components of demanding catalytic processes such as the photo-catalytic splitting of water. We have studied CeOxTiO? catalysts with low ceria loadings of 1 wt%, 3 wt% and 6 wt% that were prepared with wet impregnation methods to favor a strong interaction between CeOx and TiO?. In these materials the interfaces between CeOx-TiO? have been sequentially loaded (1%, 3% and 6%), with and without Pt (0.5 wt%). The structure and properties of the catalysts were characterized using several X-ray and electron based techniques including XRD, XPS, UPS, NEXAFS, UV-Vis and HR-STEM/STEM-EELS, to unravel the local morphology, bulk structure, surface states and electronic structure. The combination of all these techniques allow us to analyze in a systematic way the complete structural and electronic properties that prevail at the CeOx-TiO? interface. Fluorite structured nano crystallites of ceria on anatase-structured titania were identified by both XRD and NEXAFS. A sequential increasing of the CeOx loading led to the formation of clusters, then plates and finally nano particles in a hierarchical manner on the TiO? support. The electronic structures of these catalysts indicate that the interaction between TiO? and CeO? is closely related to the local morphology of nanostructured CeO?. Ce? cations were detected at the surface of CeO? and at the interface of the two oxides. In addition, the titania is perturbed by the interaction with ceria and also with Pt. The photocatalytic activity for the splitting of H?O using UV light was measured for these materials and correlated with our understanding of the electronic and structural properties. Optimal catalytic performance and photo response results were found for the 1 wt% CeOx-TiO? catalyst where low dimensional geometry of the ceria provided ideal electronic and geometrical properties. The structural and electronic properties of the interface were critical for the photocatalytic performance of this mixed-oxide nanocatalyst system.

  20. Muon neutrino charged current inclusive charged pion (CC?{sup }) production in MINER?A

    SciTech Connect (OSTI)

    Eberly, B.

    2015-05-15

    The production of charged pions by neutrinos interacting on nuclei is of great interest in nuclear physics and neutrino oscillation experiments. The MINER?A experiment is working towards releasing the worlds first high statistics neutrino pion production measurements in a few-GeV neutrino beam. We describe MINER?As CC?{sup } analysis event selection in both the neutrino and antineutrino beams, noting reconstruction resolutions and kinematic limits. We also show area-normalized data-simulation comparisons of the reconstructed muon and charged pion kinetic energy distributions.

  1. Mineral resources of the Buffalo Hump and Sand Dunes Addition Wilderness Study Areas, Sweetwater County, Wyoming

    SciTech Connect (OSTI)

    Gibbons, A.B.; Barbon, H.N.; Kulik, D.M. (Geological Survey, Reston, VA (USA)); McDonnell, J.R. Jr. (US Bureau of Mines (US))

    1990-01-01

    The authors present a study to assess the potential for undiscovered mineral resources and appraise the identified resources of the Buffalo Hump and Sand Dunes Addition Wilderness Study Areas, southwestern Wyoming, There are no mines, prospects, or mineralized areas nor any producing oil or gas wells; however, there are occurrences of coal, claystone and shale, and sand. There is a moderate resource potential for oil shale and natural gas and a low resource potential for oil, for metals, including uranium, and for geothermal sources.

  2. Iron speciation in minerals and glasses probed by M [subscript 2/3] -edge

    Office of Scientific and Technical Information (OSTI)

    X-ray Raman scattering spectroscopy (Journal Article) | SciTech Connect Iron speciation in minerals and glasses probed by M [subscript 2/3] -edge X-ray Raman scattering spectroscopy Citation Details In-Document Search Title: Iron speciation in minerals and glasses probed by M [subscript 2/3] -edge X-ray Raman scattering spectroscopy Authors: Nyrow, A. ; Sternemann, C. ; Wilke, M. ; Gordon, R.A. ; Mende, K. ; Yava ; #351 ; , H. ; Simonelli, L. ; Hiraoka, N. ; Sahle, Ch.J. ; Huotari, S. ;

  3. Type B Accident Investigation Board Report on the Head Injury to a Miner at

    Office of Energy Efficiency and Renewable Energy (EERE) Indexed Site

    the Waste Isolation Pilot Plant, Carlsbad, New Mexico - August 25, 2004 | Department of Energy on the Head Injury to a Miner at the Waste Isolation Pilot Plant, Carlsbad, New Mexico - August 25, 2004 Type B Accident Investigation Board Report on the Head Injury to a Miner at the Waste Isolation Pilot Plant, Carlsbad, New Mexico - August 25, 2004 October 15, 2004 On August 25, 2004, an employee of Washington TRU Solution, LLC (WTS) sustained a head injury when he was struck by a C-clamp and

  4. Itinerant electrons, local moments, and magnetic correlations in the pnictide superconductors CeFeAsO₁₋xFxand Sr(Fe₁₋xCox)₂As₂

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Vilmercati, Paolo; Fedorov, Alexei; Bondino, Federica; Offi, Francesco; Panaccione, Giancarlo; Lacovig, Paolo; Simonelli, Laura; McGuire, Michael A.; Sefat, Athena S. M.; Mandrus, David; et al

    2012-06-15

    A direct and element-specific measurement of the local Fe spin moment has been provided by analyzing the Fe 3s core level photoemission spectra in the parent and optimally doped CeFeAsO₁₋xFx (x = 0, 0.11) and Sr(Fe₁₋xCox)2As2 (x = 0, 0.10) pnictides. The rapid time scales of the photoemission process allowed the detection of large local spin moments fluctuating on a 10⁻¹⁵ s time scale in the paramagnetic, antiferromagnetic, and superconducting phases, indicative of the occurrence of ubiquitous strong Hund's magnetic correlations. The magnitude of the spin moment is found to vary significantly among different families, 1.3μB in CeFeAsO and 2.1μBmore » in SrFe₂As₂. Surprisingly, the spin moment is found to decrease considerably in the optimally doped samples, 0.9μB in CeFeAsO₀.₈₉F₀.₁₁ and 1.3μB in Sr(Fe₀.₉Co₀.₁)₂As₂. The strong variation of the spin moment against doping and material type indicates that the spin moments and the motion of itinerant electrons are influenced reciprocally in a self-consistent fashion, reflecting the strong competition between the antiferromagnetic superexchange interaction among the spin moments and the kinetic energy gain of the itinerant electrons in the presence of a strong Hund's coupling. By describing the evolution of the magnetic correlations concomitant with the appearance of superconductivity, these results constitute a fundamental step toward attaining a correct description of the microscopic mechanisms shaping the electronic properties in the pnictides, including magnetism and high-temperature superconductivity.« less

  5. Magnetic correlations and the anisotropic kondo effect in Ce{sub 1-x}La{sub x}Al{sub 3}.

    SciTech Connect (OSTI)

    Goremychkin, E. A.; Osborn, R.; Rainford, B. D.; Costi, T. A.; Murani, A. P.; Scott, C. A.; King, P. J. C.; Materials Science Division; Univ. of Southhampton; Univ. Karlsruhe; Inst. laue Langevin; Rutherford Appleton Lab.

    2002-09-30

    By combining the results of muon spin relaxation and inelastic neutron scattering in the heavy fermion compounds Ce{sub 1-x}La{sub x}Al{sub 3} (0.0 {le} x {le} 0.2), we show that static magnetic correlations are suppressed above a characteristic temperature, T*, by electronic dissipation rather than by thermal disorder. Below T*, an energy gap opens in the single-ion magnetic response in agreement with the predictions of the anisotropic Kondo model. Scaling arguments suggest that similar behavior may underlie the 'hidden order' in URu{sub 2}Si{sub 2}.

  6. Evidence for Anisotropic Kondo Behavior in Ce{sub 0.8}La{sub 0.2}Al{sub 3}

    SciTech Connect (OSTI)

    Goremychkin, E. A.; Osborn, R.; Rainford, B. D.; Murani, A. P.

    2000-03-06

    We have performed an inelastic neutron scattering study of the low energy spin dynamics of the heavy fermion compound Ce{sub 0.8}La {sub 0.2}Al{sub 3} as a function of temperature and external pressure up to 5 kbar. At temperatures below 3 K, the magnetic response transforms from a quasielastic form, common to many heavy fermion systems, to a single well-defined inelastic peak, which is extremely sensitive to external pressure. The scaling of the spin dynamics and the thermodynamic properties are in agreement with the predictions of the anisotropic Kondo model. (c) 2000 The American Physical Society.

  7. Neutron diffraction study of magnetic field induced behavior in the heavy Fermion Ce3Co4Sn13

    SciTech Connect (OSTI)

    Christianson, Andrew D; Goremychkin, E. A.; Gardner, J. S.; Kang, H. J.; Chung, J.-H.; Manuel, P.; Thompson, J. D.; Sarrao, J. L.; Lawrence, J. M.

    2008-01-01

    The specific heat of Ce3Co4Sn13 exhibits a crossover from heavy Fermion behavior with antiferromagnetic correlations at low field to single impurity Kondo behavior above 2 T. We have performed neutron diffraction measurements in magnetic fields up to 6 Tesla on single crystal samples. The (001) position shows a dramatic increase in intensity in field which appears to arise from static polarization of the 4f level and which at 0.14 K also exhibits an anomaly near 2T reflecting the crossover to single impurity behavior.

  8. Synthesis and crystal structure of the isotypic rare earth thioborates Ce[BS{sub 3}], Pr[BS{sub 3}], and Nd[BS{sub 3}

    SciTech Connect (OSTI)

    Hunger, Jens; Borna, Marija [Max Planck Institute for Chemical Physics of Solids, Noethnitzer Strasse 40, D-01187 Dresden (Germany); Kniep, Ruediger, E-mail: kniep@cpfs.mpg.d [Max Planck Institute for Chemical Physics of Solids, Noethnitzer Strasse 40, D-01187 Dresden (Germany)

    2010-03-15

    The orthothioborates Ce[BS{sub 3}], Pr[BS{sub 3}] and Nd[BS{sub 3}] were prepared from mixtures of the rare earth (RE) metals together with amorphous boron and sulfur summing up to the compositions CeB{sub 3}S{sub 6}, PrB{sub 5}S{sub 9} and NdB{sub 3}S{sub 6}. The following preparation routes were used: solid state reactions with maximum temperatures of 1323 K and high-pressure high-temperature syntheses at 1173 K and 3 GPa. Pr[BS{sub 3}] and Nd[BS{sub 3}] were also obtained from rare earth chlorides RECl{sub 3} and sodium thioborate Na{sub 2}B{sub 2}S{sub 5} by metathesis type reactions at maximum temperatures of 1073 K. The crystal structure of the title compounds was determined from X-ray powder diffraction data. The thioborates are isotypic and crystallize in the orthorhombic spacegroup Pna2{sub 1} (No. 33; Z=4; Ce: a=7.60738(6)A, b=6.01720(4)A, c=8.93016(6)A; Pr: a=7.56223(4)A, b=6.00876(2)A, c=8.89747(4)A; Nd: a=7.49180(3)A, b=6.00823(2)A, c=8.86197(3)A) . The crystal structures contain isolated [BS{sub 3}]{sup 3-} groups with boron in trigonal-planar coordination. The sulfur atoms form the vertices of undulated kagome nets, which are stacked along [100] according to the sequence ABAB. Within these nets every second triangle is occupied by boron and the large hexagons are centered by rare earth ions, which are surrounded by overall nine sulfur species. - Abstract: Graphical Abstract Legend (TOC Figure): Table of Contents Figure The isotypic orthothioborates Ce[BS{sub 3}], Pr[BS{sub 3}] and Nd[BS{sub 3}] were prepared using different preparation routes. The crystal structure of the title compounds was determined from X-ray powder diffraction data. The crystal structures contain isolated [BS{sub 3}]{sup 3-} groups with boron in trigonal-planar coordination. The sulfur atoms form the vertices of corrugated kagome nets (sketched with blue dotted lines), which are stacked along [100] according to the sequence ABAB. Within these nets every second triangle is occupied by boron and the large hexagons are centered by rare earth ions, which are surrounded by overall nine sulfur species.

  9. Structure and Magnetic Properties of Ce3(Ni/Al/Ga)11„A New Phase with the La3Al11 Structure Type

    Office of Scientific and Technical Information (OSTI)

    Crystals 2015, 5, 1-8; doi:10.3390/cryst5010001 crystals ISSN 2073-4352 www.mdpi.com/journal/crystals Article Structure and Magnetic Properties of Ce 3 (Ni/Al/Ga) 11 -A New Phase with the La 3 Al 11 Structure Type Oliver Janka 1,2,†, *, Tian Shang 3,4,† , Ryan E. Baumbach 3,5,† , Eric D. Bauer 3,† , Joe D. Thompson 3,† and Susan M. Kauzlarich 1,†, * 1 Department of Chemistry, University of California, Davis, CA 95616, USA 2 Institut für Anorganische und Analytische Chemie,

  10. Measure Guideline: Three High Performance Mineral Fiber Insulation Board Retrofit Solutions

    SciTech Connect (OSTI)

    Neuhauser, K.

    2015-01-01

    This Measure Guideline describes a high performance enclosure retrofit package that uses mineral fiber insulation board, and is intended to serve contractors and designers seeking guidance for non-foam exterior insulation retrofit processes. The guideline describes retrofit assembly and details for wood frame roof and walls and for cast concrete foundations.

  11. Measure Guideline: Three High Performance Mineral Fiber Insulation Board Retrofit Solutions

    SciTech Connect (OSTI)

    Neuhauser, K.

    2015-01-01

    This Measure Guideline describes a high performance enclosure retrofit package that uses mineral fiber insulation board. The Measure Guideline describes retrofit assembly and details for wood frame roof and walls and for cast concrete foundations. This Measure Guideline is intended to serve contractors and designers seeking guidance for non-foam exterior insulation retrofit.

  12. Airflow Resistance of Loose-Fill Mineral Fiber Insulations in Retrofit Applications

    SciTech Connect (OSTI)

    Schumacher, C. J.; Fox, M. J.; Lstiburek, J.

    2015-02-01

    This report expands on Building America Report 1109 by applying the experimental apparatus and test method to dense-pack retrofit applications using mineral fiber insulation materials. Three (3) fiber glass insulation materials and one (1) stone wool insulation material were tested, and the results compared to the cellulose results from the previous study.

  13. Airflow Resistance of Loose-Fill Mineral Fiber Insulations in Retrofit Applications

    SciTech Connect (OSTI)

    Schumacher, C. J.; Fox, M. J.; Lstiburek, J.

    2015-02-01

    This report expands on Building America Report 1109 by applying the experimental apparatus and test method to dense-pack retrofit applications using mineral fiber insulation materials. Three fiber glass insulation materials and one stone wool insulation material were tested, and the results compared to the cellulose results from the previous study.

  14. Mineral formation and redox-sensitive trace elements in a near-surface hydrothermal alteration system

    SciTech Connect (OSTI)

    Gehring, A.U.; Schosseler, P.M.; Weidler, P.G.

    1999-07-01

    A recent hydrothermal mudpool at the southwestern slope of the Rincon de la Vieja volcano in Northwest Costa Rica exhibits an argillic alteration system formed by intense interaction of sulfuric acidic fluids with wall rock materials. Detailed mineralogical analysis revealed an assemblage with kaolinite, alunite, and opal-C as the major mineral phases. Electron paramagnetic resonance spectroscopy (EPR) showed 3 different redox-sensitive cations associated with the mineral phases, Cu{sup +} is structure-bound in opal-C, whereas VO{sup 2+} and Fe{sup 3+} are located in the kaolinite structure. The location of the redox-sensitive cations in different minerals of the assemblage is indicative of different chemical conditions. The formation of the alteration products can be described schematically as a 2-step process. In a first step alunite and opal-C were precipitated in a fluid with slightly reducing conditions and a low chloride availability. The second step is characterized by a decrease in K{sup +} activity and subsequent formation of kaolinite under weakly oxidizing to oxidizing redox conditions as indicated by structure-bound VO{sup 2+} and Fe{sup 3+}. The detection of paramagnetic trace elements structure-bound in mineral phases by EPR provide direct information about the prevailing redox conditions during alteration and can, therefore, be used as additional insight into the genesis of the hydrothermal, near-surface system.

  15. Mineral-Surfactant Interactions for Minimum Reagents Precipitation and Adsorption for Improved Oil Recovery

    SciTech Connect (OSTI)

    P. Somasundaran

    2008-09-20

    Chemical EOR can be an effective method for increasing oil recovery and reducing the amount of produced water; however, reservoir fluids are chemically complex and may react adversely to the polymers and surfactants injected into the reservoir. While a major goal is to alter rock wettability and interfacial tension between oil and water, rock-fluid and fluid-fluid interactions must be understood and controlled to minimize reagent loss, maximize recovery and mitigate costly failures. The overall objective of this project was to elucidate the mechanisms of interactions between polymers/surfactants and the mineral surfaces responsible for determining the chemical loss due to adsorption and precipitation in EOR processes. The role of dissolved inorganic species that are dependent on the mineralogy is investigated with respect to their effects on adsorption. Adsorption, wettability and interfacial tension are studied with the aim to control chemical losses, the ultimate goal being to devise schemes to develop guidelines for surfactant and polymer selection in EOR. The adsorption behavior of mixed polymer/surfactant and surfactant/surfactant systems on typical reservoir minerals (quartz, alumina, calcite, dolomite, kaolinite, gypsum, pyrite, etc.) was correlated to their molecular structures, intermolecular interactions and the solution conditions such as pH and/or salinity. Predictive models as well as general guidelines for the use of polymer/surfactant surfactant/surfactant system in EOR have been developed The following tasks have been completed under the scope of the project: (1) Mineral characterization, in terms of SEM, BET, size, surface charge, and point zero charge. (2) Study of the interactions among typical reservoir minerals (quartz, alumina, calcite, dolomite, kaolinite, gypsum, pyrite, etc.) and surfactants and/or polymers in terms of adsorption properties that include both macroscopic (adsorption density, wettability) and microscopic (orientation/conformation of the adsorbed layers), as well as precipitation/abstraction characteristics. (3) Investigation of the role of dissolved species, especially multivalent ions, on interactions between reservoir minerals and surfactants and/or polymers leading to surfactant precipitation or activated adsorption. (4) Solution behavior tests--surface tension, interaction, ultra filtration, and other tests. (5) Surfactant-mineral interactions relative to adsorption, wettability, and electrophoresis. (6) Work on the effects of multivalent ions, pH, temperature, salinity, and mixing ratio on the adsorption. Developments of adsorption models to explain interactions between surfactants/polymers/minerals. (7) General guidelines for the use of certain surfactants, polymers and their mixtures in micelle flooding processes.

  16. A novel yellow-emitting SrAlSi{sub 4}N{sub 7}:Ce{sup 3+} phosphor for solid state lighting: Synthesis, electronic structure and photoluminescence properties

    SciTech Connect (OSTI)

    Ruan, Jian; Xie, Rong-Jun; Funahashi, Shiro; Tanaka, Yoshinori; Takeda, Takashi; Suehiro, Takayuki; Hirosaki, Naoto; Li, Yuan-Qiang

    2013-12-15

    Ce{sup 3+}-doped and Ce{sup 3+}/Li{sup +}-codoped SrAlSi{sub 4}N{sub 7} phosphors were synthesized by gas pressure sintering of powder mixtures of Sr{sub 3}N{sub 2}, AlN, ?-Si{sub 3}N{sub 4}, CeN and Li{sub 3}N. The phase purity, electronic crystal structure, photoluminescence properties of SrAlSi{sub 4}N{sub 7}:Ce{sup 3+}(Ce{sup 3+}/Li{sup +}) were investigated in this work. The band structure calculated by the DMol{sup 3} code shows that SrAlSi{sub 4}N{sub 7} has a direct band gap of 3.87 eV. The single crystal analysis of Ce{sup 3+}-doped SrAlSi{sub 4}N{sub 7} indicates a disordered Si/Al distribution and nitrogen vacnacy defects. SrAlSi{sub 4}N{sub 7} was identified as a major phase of the fired powders, and Sr{sub 5}Al{sub 5}Si{sub 21}N{sub 35}O{sub 2} and AlN as minor phases. Both Ce{sup 3+} and Ce{sup 3+}/Li{sup +} doped SrAlSi{sub 4}N{sub 7} phosphors can be efficiently excited by near-UV or blue light and show a broadband yellow emission peaking around 565 nm. A highest external quantum efficiency of 38.3% under the 450 nm excitation was observed for the Ce{sup 3+}/Li{sup +}-doped SrAlSi{sub 4}N{sub 7} (5 mol%). A white light LED lamp with color temperature of 6300 K and color rendering index of Ra=78 was achieved by combining Sr{sub 0.97}Al{sub 1.03}Si{sub 3.997}N/94/maccounttest14=t0005{sub 1}8193 {sub 7}:Ce{sup 3+}{sub 0.03} with a commercial blue InGaN chip. It indicates that SrAlSi{sub 4}N{sub 7}:Ce{sup 3+} is a promising yellow emitting down-conversion phosphor for white LEDs. - Graphical abstract: One-phosphor converted white light-emitting diode (LED) was fabricated by combining a blue LED chip and a yellow-emitting SrAlSi4N7:Ce{sup 3+} phosphor (see inset), which has the color rendering index of 78 and color temperature of 6300 K. - Highlights: We reported a new yellow nitride phosphor suitable for solid state lighting. We solved the crystal structure and evidenced a disordered Si/Al distribution. We fabricated a high color rendering white LEDs by using a single SrAlSi4N7:Ce.

  17. Appraisal of selected epidemiologic issues from studies of lung cancer among uranium and hard rock miners

    SciTech Connect (OSTI)

    Petersen, G R; Sever, L E

    1982-04-01

    An extensive body of published information about lung cancer among uranium miners was reviewed and diverse information, useful in identifying important issues but not in resolving them was found. Measuring exposure and response; thresholds of exposure; latency or the period from first mining experience to death; effort to predict excess risk of death, using a model; effects of smoking and radon daughter exposure on the histology of lung tumors; and the interplay of factors on the overall risk of death were all examined. The general concept of thresholds; that is, an exposure level below which risk does not increase was considered. The conclusion is that it should be possible to detect and estimate an epidemiologic threshold when the cohorts have been followed to the death of all members. Issues concerning latency in the studies of uranium miners published to date were examined. It is believed that the induction-latent period for lung cancer among uranium miners may be: as little as 10 to more than 40 years; dependent on age at which exposure begins; exposure rate; and ethnicity or smoking habits. Although suggested as factual, their existence is uncertain. An effect due to the exposure rate may exist although it has not been factual, their existence is uncertain. An effect due to the exposure rate may exist although it has not been confirmed. The median induction-latent period appears to be in excess of the 15 years frequently cited for US uranium miner. A distinct pattern of shorter induction-latent periods with increasing age at first mining exposure is reported. The evidence for and against an unusual histologic pattern of lung cancers among uranium miners was examined. The ratio of epidermoid to small cell types was close to 1:2; the ratio in the general population is nearer 2:1. The histologic pattern warrants closer attention of pathologists and epidemiologists. (ERB) (ERB)

  18. Effect of Tb{sup 3+} concentration on the optical and vibrational properties of YBO{sub 3} tri-doped with Eu{sup 3+}, Ce{sup 3+}, and Tb{sup 3+}

    SciTech Connect (OSTI)

    Sohal, S.; Hassanzadeh, E.; Huang, J. Y. [Department of Physics, Texas Tech University and Nano Tech Center, Lubbock, Texas 79409 (United States); Nazari, M.; Holtz, M., E-mail: mark.holtz@txstate.edu [Department of Physics, Texas State University, San Marcos, Texas 78666 (United States); Zhang, X.; Chaudhuri, J. [Department of Mechanical Engineering, Texas Tech University, Lubbock, Texas 79409 (United States); Kuryatkov, V. V. [Department of Electrical and Computer Engineering and Nano Tech Center, Texas Tech University, Lubbock, Texas 79409 (United States); Hope-Weeks, L. J. [Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, Texas 79409 (United States)

    2014-05-14

    Structural and optical studies are reported of yttrium orthoborate YBO{sub 3} when tri-doped with Eu{sup 3+}, Ce{sup 3+}, and Tb{sup 3+}, focusing on the role of terbium concentration. Incorporation of Tb{sup 3+} affects emission properties for photoluminescence (PL) excited by near ultraviolet light. For constant cerium and europium concentrations, increasing the Tb{sup 3+} results in diminished PL from the Ce{sup 3+} and Tb{sup 3+} color centers. Simultaneously, the PL excitation bands related to both Ce{sup 3+} and Tb{sup 3+} increase in intensity for red emission from the Eu{sup 3+}. Results are consistent with a Ce{sup 3+}???(Tb{sup 3+}){sub n}???Eu{sup 3+} energy transfer scheme, where (Tb{sup 3+}){sub n} denotes a chain incorporating n terbium ions. A high red to orange PL intensity ratio is obtained, ranging from 1.34 to 2.09. Raman vibrational bands show a systematic change, with Tb{sup 3+} concentration, in the B{sub 3}O{sub 9} ring terminal oxygen bending mode coordinated with the yttrium site where dopant ions substitute. The structural changes are interpreted as variations in the local neighborhood of these sites in the YBO{sub 3}:Ce{sup 3+},Tb{sup 3+},Eu{sup 3+} crystal structure.

  19. MINERALIZATION OF RADIOACTIVE WASTES BY FLUIDIZED BED STEAM REFORMING (FBSR): COMPARISONS TO VITREOUS WASTE FORMS, AND PERTINENT DURABILITY TESTING

    SciTech Connect (OSTI)

    Jantzen, C

    2008-12-26

    The Savannah River National Laboratory (SRNL) was requested to generate a document for the Washington State Department of Ecology and the U.S. Environmental Protection Agency that would cover the following topics: (1) A description of the mineral structures produced by Fluidized Bed Steam Reforming (FBSR) of Hanford type Low Activity Waste (LAW including LAWR which is LAW melter recycle waste) waste, especially the cage structured minerals and how they are formed. (2) How the cage structured minerals contain some contaminants, while others become part of the mineral structure (Note that all contaminants become part of the mineral structure and this will be described in the subsequent sections of this report). (3) Possible contaminant release mechanisms from the mineral structures. (4) Appropriate analyses to evaluate these release mechanisms. (5) Why the appropriate analyses are comparable to the existing Hanford glass dataset. In order to discuss the mineral structures and how they bond contaminants a brief description of the structures of both mineral (ceramic) and vitreous waste forms will be given to show their similarities. By demonstrating the similarities of mineral and vitreous waste forms on atomic level, the contaminant release mechanisms of the crystalline (mineral) and amorphous (glass) waste forms can be compared. This will then logically lead to the discussion of why many of the analyses used to evaluate vitreous waste forms and glass-ceramics (also known as glass composite materials) are appropriate for determining the release mechanisms of LAW/LAWR mineral waste forms and how the durability data on LAW/LAWR mineral waste forms relate to the durability data for LAW/LAWR glasses. The text will discuss the LAW mineral waste form made by FBSR. The nanoscale mechanism by which the minerals form will be also be described in the text. The appropriate analyses to evaluate contaminant release mechanisms will be discussed, as will the FBSR test results to date and how they compare to testing performed on LAW glasses. Other details about vitreous waste form durability and impacts of REDuction/OXidation (REDOX) on durability are given in Appendix A. Details about the FBSR process, various pilot scale demonstrations, and applications are given in Appendix B. Details describing all the different leach tests that need to be used jointly to determine the leaching mechanisms of a waste form are given in Appendix C. Cautions regarding the way in which the waste form surface area is measured and in the choice of leachant buffers (if used) are given in Appendix D.

  20. The role of reaction affinity and secondary minerals in regulating chemical weathering rates at the Santa Cruz Soil Chronosequence, California

    SciTech Connect (OSTI)

    Maher, K.; Steefel, C. I.; White, A.F.; Stonestrom, D.A.

    2009-02-25

    In order to explore the reasons for the apparent discrepancy between laboratory and field weathering rates and to determine the extent to which weathering rates are controlled by the approach to thermodynamic equilibrium, secondary mineral precipitation and flow rates, a multicomponent reactive transport model (CrunchFlow) was used to interpret soil profile development and mineral precipitation and dissolution rates at the 226 ka marine terrace chronosequence near Santa Cruz, CA. Aqueous compositions, fluid chemistry, transport, and mineral abundances are well characterized (White et al., 2008, GCA) and were used to constrain the reaction rates for the weathering and precipitating minerals in the reactive transport modeling. When primary mineral weathering rates are calculated with either of two experimentally determined rate constants, the nonlinear, parallel rate law formulation of Hellmann and Tisser and [2006] or the aluminum inhibition model proposed by Oelkers et al. [1994], modeling results are consistent with field-scale observations when independently constrained clay precipitation rates are accounted for. Experimental and field rates, therefore, can be reconciled at the Santa Cruz site. Observed maximum clay abundances in the argillic horizons occur at the depth and time where the reaction fronts of the primary minerals overlap. The modeling indicates that the argillic horizon at Santa Cruz can be explained almost entirely by weathering of primary minerals and in situ clay precipitation accompanied by undersaturation of kaolinite at the top of the profile. The rate constant for kaolinite precipitation was also determined based on model simulations of mineral abundances and dissolved Al, SiO{sub 2}(aq) and pH in pore waters. Changes in the rate of kaolinite precipitation or the flow rate do not affect the gradient of the primary mineral weathering profiles, but instead control the rate of propagation of the primary mineral weathering fronts and thus total mass removed from the weathering profile. Our analysis suggests that secondary clay precipitation is as important as aqueous transport in governing the amount of dissolution that occurs within a profile because clay minerals exert a strong control over the reaction affinity of the dissolving primary minerals. The modeling also indicates that the weathering advance rate and the total mass of mineral dissolved is controlled by the thermodynamic saturation of the primary dissolving phases plagioclase and K-feldspar, as is evident from the difference in propagation rates of the reaction fronts for the two minerals despite their very similar kinetic rate laws.

  1. Nodal to nodeless superconducting energy-gap structure change concomitant with Fermi-surface reconstruction in the heavy-fermion compound CeCoIn5

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Kim, Hyunsoo; Tanatar, M. A.; Flint, R.; Petrovic, C.; Hu, Rongwei; White, B. D.; Lum, I. K.; Maple, M. B.; Prozorov, R.

    2015-01-15

    The London penetration depth λ(T) was measured in single crystals of Ce1–xRxCoIn₅, R=La, Nd, and Yb down to Tmin ≈ 50 mK (Tc/Tmin ~50) using a tunnel-diode resonator. In the cleanest samples Δλ(T) is best described by the power law, Δλ(T) ∝ Tn, with n ~ 1, consistent with line nodes. Substitutions of Ce with La, Nd, and Yb lead to similar monotonic suppressions of Tc, however, the effects on Δλ(T) differ. While La and Nd dopings lead to increase of the exponent n and saturation at n ~ 2, as expected for a dirty nodal superconductor, Yb doping leadsmore » to n > 3, suggesting a change from nodal to nodeless superconductivity. As a result, this superconducting gap structure change happens in the same doping range where changes of the Fermi surface topology were reported, implying that the nodal structure and Fermi surface topology are closely linked.« less

  2. Investigation of Mineral Transformations in Wet Supercritical CO2 by Electron Microscopy

    SciTech Connect (OSTI)

    Arey, Bruce W.; Kovarik, Libor; Wang, Zheming; Felmy, Andrew R.

    2011-10-10

    The capture and storage of carbon dioxide and other greenhouse gases in deep geologic formations represents one of the most promising options for mitigating the impacts of greenhouse gases on global warming. In this regard, mineral-fluid interactions are of prime importance since such reactions can result in the long term sequestration of CO2 by trapping in mineral phases. Recently it has been recognized that interactions with neat to water-saturated non-aqueous fluids are of prime importance in understanding mineralization reactions since the introduced CO2 is likely to contain water initially or soon after injection and the supercritical CO2 (scCO2) is less dense than the aqueous phase which can result in a buoyant scCO2 plume contacting the isolating caprock. As a result, unraveling the molecular/microscopic mechanisms of mineral transformation in neat to water saturated scCO2 has taken on an added important. In this study, we are examining the interfacial reactions of the olivine mineral forsterite (Mg2SiO4) over a range of water contents up to and including complete water saturation in scCO2. The surface precipitates that form on the reacted forsterite grains are extremely fragile and difficult to experimentally characterize. In order to address this issue we have developed experimental protocols for preparing and imaging electron-transparent samples from fragile structures. These electron-transparent samples are then examined using a combination of STEM/EDX, FIB-TEM, and helium ion microscope (HIM) imaging (Figures 1-3). This combination of capabilities has provided unique insight into the geochemical processes that occur on scCO2 reacted mineral surfaces. The experimental procedures and protocols that have been developed also have useful applications for examining fragile structures on a wide variety of materials. This research was performed using EMSL, a national scientific user facility sponsored by the Department of Energy's Office of Biological and Environmental Research located at Pacific Northwest National Laboratory.

  3. Energy efficient microwave synthesis of mesoporous Ce0.5M0.5O2 (Ti, Zr, Hf) nanoparticles for low temperature CO oxidation in an ionic liquid – a comparative study

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Alammar, Tarek; Chow, Ying -Kit; Mudring, Anja -Verena

    2014-11-19

    Ce0.5M0.5O2 (M = Ti, Zr, Hf) nanoparticles have been successfully synthesized by microwave irradiation in the ionic liquid [C4mim][Tf2N] (1-butyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide). The morphology, crystallinity, and chemical composition of the obtained materials were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), energy dispersive X-ray spectroscopy (EDX), Raman spectroscopy, and N2–adsorption measurements. XRD and Raman spectroscopy analyses confirmed the formation of solid solutions with cubic fluorite structure. The catalytic activities of the Ce0.5M0.5O2 (M = Ti, Zr, Hf) nanoparticles were investigated in the low-temperature oxidation of CO. Ce0.5Zr0.5O2 nanospheres exhibit the best performance (100% conversion at 350 °C), followed by Ce0.5Hf0.5O2more » (55% conversion at 360 °C) and Ce0.5Ti0.5O2 (11% conversion at 350 °C). Heating the as-prepared Ce0.5Zr0.5O2 to 600 °C for extended time leads to a decrease in surface area and, as expected decreased catalytic activity. Depending on the ionic liquid the obtained Ce0.5Zr0.5O2 exhibits different morphologies, varying from nano-spheres in [C4mim][Tf2N] and [P66614][Tf2N] (P66614 = trishexyltetradecylphosphonium) to sheet-like assemblies in [C3mimOH][Tf2N] (C3mimOH = 1-(3-hydroxypropyl)-3-methylimidazolium). As a result, the microwave synthesis superiority to other heating methods like sonochemical synthesis and conventional heating was proven by comparative experiments where the catalytic activity of Ce0.5Zr0.5O2 obtained by alternate methods such as conventional heating was found to be poorer than that of the microwave-synthesised material.« less

  4. Mineral resources of the Cross Mountain Wilderness Study Area, Moffat County, Colorado

    SciTech Connect (OSTI)

    Evans, K.V.; Frisken, J.G.; Kulik, D.M.; Thompson, J.R.

    1989-01-01

    The Cross Mountain Wilderness Study Area, in northwestern Colorado, contains high-purity limestone suitable for industrial and agricultural use; dolomitic limestone suitable for agricultural use; and limestone, dolomite, sandstone, and sand and gravel suitable for use as construction materials. There has been no mining within this study area. This entire study area has a low mineral resource potential for sediment-hosted copper in the Uinta Mountain Group, and parts of this study area have a low resource potential for sandstone-type uranium-vanadium in sedimentary rocks. The entire study area has a low resource potential for all other metals and geothermal resources. It has a high energy resource potential for oil and gas in the eastern part of the area and moderate potential elsewhere. This study area has no mineral resource potential for coal.

  5. Method for the production of mineral wool and iron from serpentine ore

    DOE Patents [OSTI]

    O'Connor, William K. (Albany, OR); Rush, Gilbert E. (Scio, OR); Soltau, Glen F. (Lebanon, OR)

    2011-10-11

    Magnesium silicate mineral wools having a relatively high liquidus temperature of at least about 1400.degree. C. and to methods for the production thereof are provided. The methods of the present invention comprise melting a magnesium silicate feedstock (e.g., comprising a serpentine or olivine ore) having a liquidus temperature of at least about 1400.degree. C. to form a molten magnesium silicate, and subsequently fiberizing the molten magnesium silicate to produce a magnesium silicate mineral wool. In one embodiment, the magnesium silicate feedstock contains iron oxide (e.g., up to about 12% by weight). Preferably, the melting is performed in the presence of a reducing agent to produce an iron alloy, which can be separated from the molten ore. Useful magnesium silicate feedstocks include, without limitation, serpentine and olivine ores. Optionally, silicon dioxide can be added to the feedstock to lower the liquidus temperature thereof.

  6. Comparison of Caprock Mineral Characteristics at Field Demonstration Sites for Saline Aquifer Sequestration of Carbon Dioxide

    SciTech Connect (OSTI)

    Griffith, C.A.; Lowry, G. (Carnegie Mellon University); Dzombak, D. (Carnegie Mellon University); Soong, Yee; Hedges, S.W.

    2008-10-01

    In 2003 the U.S Department of Energy initiated regional partnership programs to address the concern for rising atmospheric CO2. These partnerships were formed to explore regional and economical means for geologically sequestering CO2 across the United States and to set the stage for future commercial applications. Several options exist for geological sequestration and among these sequestering CO2 into deep saline aquifers is one of the most promising. This is due, in part, to the possibility of stabilized permanent storage through mineral precipitation from chemical interactions of the injected carbon dioxide with the brine and reservoir rock. There are nine field demonstration sites for saline sequestration among the regional partnerships in Phase II development to validate the overall commercial feasibility for CO2 geological sequestration. Of the nine sites considered for Phase II saline sequestration demonstration, seven are profiled in this study for their caprock lithologic and mineral characteristics.

  7. Overview of mineral waste form development for the electrometallurgical treatment of spent nuclear fuel

    SciTech Connect (OSTI)

    Pereira, C.; Lewis, M.A.; Ackerman, J.P.

    1996-05-01

    Argonne is developing a method to treat spent nuclear fuel in a molten salt electrorefiner. Wastes from this treatment will be converted into metal and mineral forms for geologic disposal. A glass-bonded zeolite is being developed to serve as the mineral waste form that will contain the fission products that accumulate in the electrorefiner salt. Fission products are ion exchanged from the salt into the zeolite A structure. The crystal structure of the zeolite after ion exchange is filled with salt ions. The salt-loaded zeolite A is mixed with glass frit and hot pressed. During hot pressing, the zeolite A may be converted to sodalite which also retains the waste salt. The glass-bonded zeolite is leach resistant. MCC-1 testing has shown that it has a release rate below 1 g/(m{sup 2}day) for all elements.

  8. Contact metasomatic and hydrothermal minerals in the SH2 deep well, Sabatini Volcanic District, Latium, Italy

    SciTech Connect (OSTI)

    Cavarretta, G.; Tecce, F.

    1987-01-01

    Metasomatic and hydrothermal minerals were logged throughout the SH2 geothermal well, which reached a depth of 2498 m in the Sabatini volcanic district. Below 460 m of volcanics, where the newly formed minerals were mainly chlorite, calcite and zeolites (mostly phillipsite), drilling entered the Allochthonous Flysch Complex. Evidence of the ''Cicerchina facies'' was found down to 1600 m depth. Starting from 1070 m, down to hole bottom, a contact metasomatic complex was defined by the appearance of garnet. Garnet together with K-fledspar, vesuvianite, wilkeite, cuspidine, harkerite, wollastonite and apatite prevail in the top part of the contact metasomatic complex. Vesuvianite and phlogopite characterize the middle part. Phlogopite, pyroxene, spinel and cancrinite predominate in the bottom part. The 1500 m thick metasomatic complex indicates the presence at depth of the intrusion of a trachytic magma which released hot fluids involved in metasomatic mineral-forming reactions. Minerals such as harkerite, wilkeite, cuspidine, cancrinite, vesuvianite and phlogopite indicate the intrusive melt had a high volatile content which is in agreement with the very high explosivity index of this volcanic district. The system is at present sealed by abundant calcite and anhydrite. It is proposed that most, if not all, of the sulphates formed after reaction of SO/sub 2/ with aqueous calcium species rather than from sulphates being remobilized from evaporitic (Triassic) rocks as previously inferred. The hypothesis of a CO/sub 2/-rich deep-derived fluid ascending through major fracture systems and contrasting cooling in the hottest areas of Latium is presented.

  9. Synchrotron X-ray Investigations of Mineral-Microbe-Metal Interactions

    SciTech Connect (OSTI)

    Kemner, Kenneth M.; O'Loughlin, Edward J.; Kelly, Shelly D.; Boyanov, Maxim I.

    2008-06-06

    Interactions between microbes and minerals can play an important role in metal transformations (i.e. changes to an element's valence state, coordination chemistry, or both), which can ultimately affect that element's mobility. Mineralogy affects microbial metabolism and ecology in a system; microbes, in turn, can affect the system's mineralogy. Increasingly, synchrotron-based X-ray experiments are in routine use for determining an element's valence state and coordination chemistry, as well as for examining the role of microbes in metal transformations.

  10. Dewatering: Coal and mineral processing. (Latest citations from the COMPENDEX database). Published Search

    SciTech Connect (OSTI)

    Not Available

    1993-05-01

    The bibliography contains citations concerning the technology of dewatering. Included is coverage of techniques, processes, and evaluations applied to coal processing, coal slurry preparation, ash treatments, and processing of other mineral ores. Mechanical devices, heating devices, filtering techniques, air drying, the use of surfactants and flocculants, and design techniques in dewatering systems are discussed. Dewatering of peats, sewage sludges, and industrial sludges are referenced in related bibliographies. (Contains 250 citations and includes a subject term index and title list.)

  11. Understanding Mineral Transport in Switchgrass | U.S. DOE Office of Science

    Office of Science (SC) Website

    (SC) Understanding Mineral Transport in Switchgrass Biological and Environmental Research (BER) BER Home About Research Facilities Science Highlights Searchable Archive of BER Highlights External link Benefits of BER Funding Opportunities Biological & Environmental Research Advisory Committee (BERAC) Community Resources Contact Information Biological and Environmental Research U.S. Department of Energy SC-23/Germantown Building 1000 Independence Ave., SW Washington, DC 20585 P: (301)

  12. Method to enhance the concentration of valuable minerals in froth flotation

    Broader source: All U.S. Department of Energy (DOE) Office Webpages (Extended Search)

    process used in mining - Energy Innovation Portal Find More Like This Return to Search Method to enhance the concentration of valuable minerals in froth flotation process used in mining Enhancing Selectivity and Recovery in the Fractional Flotation of Flotation Column Particles National Energy Technology Laboratory Contact NETL About This Technology Publications: PDF Document Publication Method for Enhancing Selectivity and Recovery in the Fractional Flotation of Flotation Column Particles

  13. Molecular Dynamics Simulation and Analysis of Interfacial Water at Selected Sulfide Mineral Surfaces under Anaerobic Conditions

    SciTech Connect (OSTI)

    Jin, Jiaqi; Miller, Jan D.; Dang, Liem X.

    2014-04-10

    In this paper, we report on a molecular dynamics simulation (MDS) study of the behavior of interfacial water at selected sulfide mineral surfaces under anaerobic conditions. The study revealed the interfacial water structure and wetting characteristics of the pyrite (100) surface, galena (100) surface, chalcopyrite (012) surface, sphalerite (110) surface, and molybdenite surfaces (i.e., the face, armchair-edge, and zigzag-edge surfaces), including simulated contact angles, relative number density profiles, water dipole orientations, hydrogen-bonding, and residence times. For force fields of the metal and sulfur atoms in selected sulfide minerals used in the MDS, we used the universal force field (UFF) and another set of force fields optimized by quantum chemical calculations for interactions with interfacial water molecules at selected sulfide mineral surfaces. Simulation results for the structural and dynamic properties of interfacial water molecules indicate the natural hydrophobic character for the selected sulfide mineral surfaces under anaerobic conditions as well as the relatively weak hydrophobicity for the sphalerite (110) surface and two molybdenite edge surfaces. Part of the financial support for this study was provided by the U.S. Department of Energy (DOE) under Basic Science Grant No. DE-FG-03-93ER14315. The Division of Chemical Sciences, Geosciences, and Biosciences, Office of Basic Energy Sciences (BES), of the DOE, funded work performed by Liem X. Dang. Battelle operates Pacific Northwest National Laboratory for DOE. The calculations were carried out using computer resources provided by BES. The authors are grateful to Professor Tsun-Mei Chang for valuable discussions.

  14. I HEAVY MINERALS CO. 836 South Michigan Avenue Chic&o-5, Illinois

    Office of Legacy Management (LM)

    .,., f.IE.' ,4-L ,.4 ., " - * _ .c - ,: ~, , .' " I HEAVY MINERALS CO. / 836 South Michigan Avenue Chic&o-5, Illinois December 1, 1954 , etomic Energy Commiesion Raw Materials Division Washington, D. C. - - Attention: Mr. Radford Faulkner Gentlemen: CRUDE THORIUM HYDROXIDE We propose to sell crude thorium hydroxide to the Atomic Energy Commission over a four year period, starting during the fourth quarter of 1955. The crude thorium hydroxide we propose to supply will be produced by

  15. Carbon Mineralization by Aqueous Precipitation for Beneficial Use of CO2 from Flue Gas

    SciTech Connect (OSTI)

    Devenney, Martin; Gilliam, Ryan; Seeker, Randy

    2014-06-01

    The objective of this project is to demonstrate an innovative process to mineralize CO2 from flue gas directly to reactive carbonates and maximize the value and versatility of its beneficial use products. The program scope includes the design, construction, and testing of a CO2 Conversion to Material Products (CCMP) Pilot Demonstration Plant utilizing CO2 from the flue gas of a power production facility in Moss Landing, CA as well as flue gas from coal combustion. This topical report covers Phase 2b, which is the construction phase of pilot demonstration subsystems that make up the integrated plant. The subsystems included are the mineralization subsystem, the Alkalinity Based on Low Energy (ABLE) subsystem, the waste calcium oxide processing subsystem, and the fiber cement board production subsystem. The fully integrated plant is now capable of capturing CO2 from various sources (gas and coal) and mineralizing into a reactive calcium carbonate binder and subsequently producing commercial size (4ftx8ft) fiber cement boards. The topical report provides a description of the “as built” design of these subsystems and the results of the commissioning activities that have taken place to confirm operability. At the end of Phase 2b, the CCMP pilot demonstration is fully ready for testing.

  16. Spirometry variability criteria--association with respiratory morbidity and mortality in a cohort of coal miners

    SciTech Connect (OSTI)

    Kellie, S.E.; Attfield, M.D.; Hankinson, J.L.; Castellan, R.M.

    1987-03-01

    To clarify the association between spirometry variability and respiratory morbidity and mortality, the authors analyzed data for miners examined in the first round of the National Coal Study, 1969-1971, and they compared groups of miners who failed with those who met each of two spirometry variability criteria: a 5% criterion recommended by the American Thoracic Society, and a 200 ml criterion used in prior research studies. Compared with miners who met the 5% criterion (the best two forced vital capacities must be within 5% or 100 ml of one another), the group that failed had a lower mean for forced expiratory volume in one second (FEV1), and odds ratios for cough, phlegm, wheeze, shortness of breath, and death of 1.75, 1.67, 1.76, 2.71, and 1.30, respectively. The findings for the 200 ml criterion (the best two FEV1s must be within 200 ml of one another) were somewhat different. The group that failed versus the group that met this criterion had a higher mean for FEV1, and odds ratios for cough, phlegm, wheeze, shortness of breath, and death of 1.13, 1.07, 1.15, 1.43, and 0.94, respectively. Although the findings differ for the two criteria, the findings demonstrate that increased spirometry variability is associated with poorer health.

  17. Oxidative Mineralization and Characterization of Polyvinyl Alcohol Solutions for Wastewater Treatment

    SciTech Connect (OSTI)

    Oji, L.N.

    2003-08-07

    Photochemical and ultrasonic treatment of polyvinyl alcohol (PVA), derived from PVA fabric material, with hydrogen peroxide was evaluated as a primary method for PVA mineralization into simpler organic molecules. PVA-based waste streams have been found to be compatible with nuclear process wastewater treatment facilities only when solubilized PVA is more than 90 percent mineralized with hydrogen peroxide. No undesirable solid particles are formed with other nuclear process liquid waste when they are mixed, pH adjusted, evaporated and blended with this type of oxidized PVA waste streams. The presence of oxidized PVA in a typical nuclear process wastewater has been found to have no detrimental effect on the efficiency of ion exchange resins, inorganic, and precipitation agents used for the removal of radionuclides from nuclear waste streams. The disappearance of PVA solution in hydrogen peroxide with ultrasonic/ ultraviolet irradiation treatment was characterized by pseudo-first-order reaction kinetics. Radioactive waste contaminated PVA fabric can be solubilized and mineralized to produce processible liquid waste, hence, no bulky solid waste disposal cost can be incurred and the radionuclides can be effectively recovered. Therefore, PVA fabric materials can be considered as an effective substitute for cellulose fabrics that are currently used in radioactive waste decontamination processes.

  18. Fundamental Thermodynamics of Actinide-Bearing Mineral Waste Forms - Final Report

    SciTech Connect (OSTI)

    Williamson, Mark A.; Ebbinghaus, Bartley B.; Navrotsky, Alexandra

    2001-03-01

    The end of the Cold War raised the need for the technical community to be concerned with the disposition of excess nuclear weapon material. The plutonium will either be converted into mixed-oxide fuel for use in nuclear reactors or immobilized in glass or ceramic waste forms and placed in a repository. The stability and behavior of plutonium in the ceramic materials as well as the phase behavior and stability of the ceramic material in the environment is not well established. In order to provide technically sound solutions to these issues, thermodynamic data are essential in developing an understanding of the chemistry and phase equilibria of the actinide-bearing mineral waste form materials proposed as immobilization matrices. Mineral materials of interest include zircon, zirconolite, and pyrochlore. High temperature solution calorimetry is one of the most powerful techniques, sometimes the only technique, for providing the fundamental thermodynamic data needed to establish optimum material fabrication parameters, and more importantly understand and predict the behavior of the mineral materials in the environment. The purpose of this project is to experimentally determine the enthalpy of formation of actinide orthosilicates, the enthalpies of formation of actinide substituted zirconolite and pyrochlore, and develop an understanding of the bonding characteristics and stabilities of these materials.

  19. Wilderness study area, mineral resources of the Sleeping Giant, Lewis and Clark County, Montana

    SciTech Connect (OSTI)

    Tysdal, G.; Reynold, M.W.; Carlson, R.R.; Kleinkopf, M.D.; Rowan, L.C. ); Peters, T.J. )

    1991-01-01

    A Mineral resource survey was conducted in 1987 by the U.S. Geological Survey and the U.S. Bureau of Mines to evaluate mineral resources (known) and mineral resource potential (undiscovered) of the Sleeping Giant Wilderness Study Area (MT-075-111) in Lewis and Clark County, Montana. The only economic resource in the study area is an inferred 1.35-million-ton reserve of decorative stone (slate); a small gold placer resource is subeconomic. A high resource potential for decorative slate exists directly adjacent to the area of identified slate resource and in the northeastern part of the study area. The rest of the study area has a low potential for decorative slate. The westernmost part of the study area has a moderate resource potential for copper and associated silver in state-bound deposits in green beds and limestone; potential is low in the rest of the study are. The study area has a low resource potential for sapphires in placer deposits, gold in placer deposits (exclusive of subeconomic resource mentioned above), phosphate in the Spokane Formation, diatomite in lake deposits, uranium, oil, gas, geothermal energy, and no resource potential for phosphate in the Phosphoria Formation.

  20. Low pressure CO? hydrogenation to methanol over gold nanoparticles activated on a CeOx/TiO? interface

    SciTech Connect (OSTI)

    Yang, Xiaofang; Boscoboinik, J. Anibal; Kattel, Shyam; Senanayake, Sanjaya D.; Nie, Xiaowa; Graciani, Jesus; Rodriguez, Jose A.; Liu, Ping; Stacchiola, Dario J.; Chen, Jingguang G.

    2015-07-28

    Capture and recycling of CO? into valuable chemicals such as alcohols could help mitigate its emissions into the atmosphere. Due to its inert nature, the activation of CO? is a critical step in improving the overall reaction kinetics during its chemical conversion. Although pure gold is an inert noble metal and cannot catalyze hydrogenation reactions, it can be activated when deposited as nanoparticles on the appropriate oxide support. In this combined experimental and theoretical study, it is shown that an electronic polarization at the metaloxide interface of Au nanoparticles anchored and stabilized on a CeOx/TiO? substrate generates active centers for CO? adsorption and its low pressure hydrogenation, leading to a higher selectivity toward methanol. In conclusion, this study illustrates the importance of localized electronic properties and structure in catalysis for achieving higher alcohol selectivity from CO? hydrogenation.

  1. Electronic structure of Ce?RhIn?: A two-dimensional heavy-fermion system studied by angle-resolved photoemission spectroscopy

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Jiang, Rui; Petrovic, C.; Mou, Daixing; Liu, Chang; Zhao, Xin; Yao, Yongxin; Ryu, Hyejin; Ho, Kai -Ming; Kaminski, Adam

    2015-04-01

    We use angle-resolved photoemission spectroscopy (ARPES) to study the 2D heavy fermion superconductor, Ce?RhIn?. The Fermi surface is rather complicated and consists of several hole and electron pockets with one of the sheets displaying strong nesting properties with a q-vector of (0.32, 0.32) ?/a. We do not observe kz dispersion of the Fermi sheets, which is consistent with the expected 2D character of the electronic structure. Comparison of the ARPES data to band structure calculations suggests that a localized picture of the f-electrons works best. While there is some agreement in the overall band dispersion and location of the Fermimoresheets, the model does not reproduce all observed bands and is not completely accurate for those it does. Our data paves the way for improving the band structure calculations and the general understanding of the transport and thermodynamical properties of this material.less

  2. 15N2 formation and fast oxygen isotope exchange during pulsed 15N18O exposure of MnOx/CeO2

    SciTech Connect (OSTI)

    Kwak, Ja Hun; Szanyi, Janos

    2014-12-23

    Pulsing 15N18O onto an annealed 1% Mn16Ox/Ce16O2 catalyst resulted in very fast oxygen isotope exchange and 15N2 formation at 295 K. In the 1st 15N18O pulse, due to the presence of large number of surface oxygen defects, extensive 15N218O and 15N2 formations were observed. In subsequent pulses oxygen isotope exchange dominated as a result of highly labile oxygen in the oxide. We gratefully acknowledge the US Department of Energy (DOE), Office of Energy Efficiency and Renewable Energy/Vehicle Technologies Program for the support of this work. The research described in this paper was performed at the Environmental Molecular Sciences Laboratory (EMSL), a national scientific user facility sponsored by the DOEs Office of Biological and Environmental Research and located at Pacific Northwest National Laboratory (PNNL). PNNL is operated for the US DOE by Battelle.

  3. Influence of the Electronic Structure and Optical Properties of CeO2 and UO2 for Characterization with UV-Laser Assisted Atom Probe Tomography

    SciTech Connect (OSTI)

    Billy Valderrama; H.B. Henderson; C. Yablinsky; J. Gan; T.R. Allen; M.V. Manuel

    2015-09-01

    Oxide materials are used in numerous applications such as thermal barrier coatings, nuclear fuels, and electrical conductors and sensors, all applications where nanometer-scale stoichiometric changes can affect functional properties. Atom probe tomography can be used to characterize the precise chemical distribution of individual species and spatially quantify the oxygen to metal ratio at the nanometer scale. However, atom probe analysis of oxides can be accompanied by measurement artifacts caused by laser-material interactions. In this investigation, two technologically relevant oxide materials with the same crystal structure and an anion to cation ratio of 2.00, pure cerium oxide (CeO2) and uranium oxide (UO2) are studied. It was determined that electronic structure, optical properties, heat transfer properties, and oxide stability strongly affect their evaporation behavior, thus altering their measured stoichiometry, with thermal conductance and thermodynamic stability being strong factors.

  4. Phases in ceria-zirconia binary oxide (1-x)CeO2-xZrO2 nanoparticles: the size effects

    SciTech Connect (OSTI)

    Zhang,F.; Chen, C.; Hanson, J.; Herman, I.; Chan, S.

    2006-01-01

    The phases of ceria-zirconia nanoparticles observed in air are studied as a function of particle size and composition by X-ray diffraction, transmission electron microscopy, and Raman spectroscopy. The emergence of two tetragonal phases t{prime}{prime} and t monotonically moves toward higher zirconia concentrations with decreasing particle size. A smaller particle size increases the solubility of zirconia in cubic ceria, while higher zirconia content in ceria stabilizes against coarsening. In particular, the cubic Ce{sub 1-x}Zr{sub x}O{sub 2-y} is persistent and is 8% in phase amount even at 90% zirconia with 33 nm crystal size. Neither the monoclinic phase m nor the tetragonal phase t{prime} is observed in the present nanoparticles (<40 nm). The effectiveness of these nanoparticles as oxygen source-and-sink in catalytic support is largely due to the persistence of the cubic and the t{prime}{prime} phases.

  5. Structure and physical properties of single crystal PrCr{sub 2}Al{sub 20} and CeM{sub 2}Al{sub 20} (M=V, Cr): A comparison of compounds adopting the CeCr{sub 2}Al{sub 20} structure type

    SciTech Connect (OSTI)

    Kangas, Michael J.; Schmitt, Devin C.; Sakai, Akito; Nakatsuji, Satoru; Institute of Solid State Physics, University of Tokyo, Kashiwa, Chiba 277-8581 ; Chan, Julia Y.

    2012-12-15

    Crystal growth and full structure determination of compounds adopting the CeCr{sub 2}Al{sub 20} structure type, LnTi{sub 2}Al{sub 20} (Ln=La-Pr, Sm, and Yb), LnV{sub 2}Al{sub 20} (Ln=La-Pr, and Sm), and LnCr{sub 2}Al{sub 20} (Ln=La-Pr, Sm, and Yb), are reported. Resistivity, magnetic susceptibility, and heat capacity of flux grown single crystals of the nonmagnetic CeM{sub 2}Al{sub 20} (Ln=Ce, Yb; M=Ti, V) compounds are compared to PrCr{sub 2}Al{sub 20}. Of particular interest is PrCr{sub 2}Al{sub 20} which does not show any phase transition down to the lowest temperature of the measurement (400 mK in resistivity measurement and 1.8 K for magnetic susceptibility measurements) and exhibits Kondo behavior at low temperatures. - Graphical abstract: Crystal structure of SmV{sub 2}Al{sub 20} showing the interpenetrating diamond-like samarium network and pyrochlore-like vanadium network. Highlights: Black-Right-Pointing-Pointer Single crystals of LnM{sub 2}Al{sub 20} were grown from a molten aluminum flux. Black-Right-Pointing-Pointer Magnetic, electrical, and specific heat of single crystal LnM{sub 2}Al{sub 20} are presented. Black-Right-Pointing-Pointer PrCr{sub 2}Al{sub 20} exhibits evidence of Kondo effect.

  6. Structure and magnetic properties of RE{sub 2}CuIn{sub 3} (RE=Ce, Pr, Nd, Sm and Gd)

    SciTech Connect (OSTI)

    Tyvanchuk, Yuriy B. Szytula, Andrzej; Zarzycki, Arkadiusz; Rodewald, Ute Ch.; Kalychak, Yaroslav M.; Poettgen, Rainer

    2008-12-15

    The ternary copper indides RE{sub 2}CuIn{sub 3}{identical_to}RECu{sub 0.5}In{sub 1.5} (RE=Ce, Pr, Nd, Sm and Gd) were synthesized from the elements in sealed tantalum tubes in an induction furnace. They crystallize with the CaIn{sub 2}-type structure, space group P6{sub 3}/mmc, with a statistical occupancy of copper and indium on the tetrahedral substructure. These indides show homogeneity ranges RECu{sub x}In{sub 2-x}. Single crystal structure refinements were performed for five crystals: CeCu{sub 0.66}In{sub 1.34} (a=479.90(7) pm, c=768.12(15) pm), PrCu{sub 0.52}In{sub 1.48} (a=480.23(7) pm, c=759.23(15) pm), NdCu{sub 0.53}In{sub 1.47} (a=477.51(7) pm, c=756.37(15) pm), SmCu{sub 0.46}In{sub 1.54} (a=475.31(7) pm, c=744.77(15) pm), and GdCu{sub 0.33}In{sub 1.67} (a=474.19(7), c=737.67(15) pm). Temperature-dependent susceptibility measurements show antiferromagnetic ordering at T{sub N}=4.7 K for Pr{sub 2}CuIn{sub 3} and Nd{sub 2}CuIn{sub 3} and 15 K for Sm{sub 2}CuIn{sub 3}. Fitting of the susceptibility data of the samarium compound revealed an energy gap {delta}E=39.7(7) K between the ground and the first excited levels. - Graphical abstract: The CaIn{sub 2}-type structure of Sm{sub 2}CuIn{sub 3}.

  7. Smoking cessation among coal miners as predicted by baseline respiratory function and symptoms: a 5-year prospective study

    SciTech Connect (OSTI)

    Ames, R.G.; Hall, D.S.

    1985-03-01

    A prospective analysis was used to test whether respiratory impairment or the presence of respiratory symptoms predicts 5-year cigarette smoking cessation in a sample of 1,118 U.S. white, male, underground coal miners. Miners were examined in 1977 and re-examined in 1982 by NIOSH, and all miners with test abnormalities were so informed by letter. Respiratory impairment was measured by an index of airways obstruction combining the spirometric measures of Forced Vital Capacity (FVC) and Forced Expiratory Volume in 1 sec (FEV1). Bronchitis symptoms were measured by an index that combined chronic cough (3+ months/year) and chronic phlegm (3 + months/year). Among these coal miners, the presence of chronic respiratory symptoms initially was inversely associated with cigarette smoking cessation. Respiratory impairment, however, was positively associated with cigarette smoking cessation but did not reach statistical significance.

  8. The use of the scanning electron microscope in the determination of the mineral composition of Ballachulish slate

    SciTech Connect (OSTI)

    Walsh, Joan A.

    2007-11-15

    Slate is a fine-grained, low-grade metamorphic rock derived from argillaceous sediments or occasionally volcanic ash. Although most slates contain mainly quartz, chlorite and white mica, they vary considerably in their durability, some lasting centuries while others fail after a few years of service. A detailed characterisation of their mineralogy is required for the assessment of performance, and to establish the provenance of a used slate. A combination of methods was used to examine Ballachulish slates; XRD analysis to determine the principal minerals present, XRF analysis to determine the total chemical composition, and scanning electron microscopy to determine the chemical composition of individual minerals. It was found that the white mica in Ballachulish slate is phengite and the chlorite is ripidolite. Feldspar is present as albite and carbonate as ferroan dolomite. Several accessory minerals were also identified, including chloritoid, monzonite and zircon. There was considerable variation in the ratio of the principal minerals, making it impossible to identify used slates by this criterion. Instead, chemical composition of the individual minerals, and possibly key accessory minerals, should be used to determine the provenance of slates.

  9. On phase equilibria and crystal structures in the systems Ce-Pd-B and Yb-Pd-B. Physical properties of R{sub 2}Pd{sub 13.6}B{sub 5} (R=Yb, Lu)

    SciTech Connect (OSTI)

    Sologub, Oksana; Rogl, Peter; Salamakha, Leonid; Bauer, Ernst; Hilscher, Gerfried; Michor, Herwig; Giester, Gerald

    2010-05-15

    Phase equilibria and crystal structures of ternary compounds were determined in the systems Ce-Pd-B and Yb-Pd-B at 850 deg. C in the concentration ranges up to 45 and 33 at% of Ce and Yb, respectively, employing X-ray single crystal and powder diffraction. Phase relations in the Ce-Pd-B system at 850 deg. C are governed by formation of extended homogeneity fields, tau{sub 2}-CePd{sub 8}B{sub 2-x} (0.10Ce{sub 3}Pd{sub 25-x}B{sub 8-y} (1.06CePd{sub 3}B{sub x} (0CePd{sub 3}. Crystallographic parameters for the new structure type tau{sub 2}-CePd{sub 8}B{sub 2-x} (space group C2/c, a=1.78104(4) nm, b=1.03723(3) nm, c=1.16314(3), beta=118.515(1){sup o} for x=0.46) were established from X-ray single crystal diffraction. The crystal structures of tau{sub 2}-CePd{sub 8}B{sub 2-x} and tau{sub 3}-Ce{sub 3}Pd{sub 25-x}B{sub 3-y} are connected in a crystallographic group-subgroup relationship. Due to the lack of suitable single crystals, the novel structure of tau{sub 1}-Ce{sub 6}Pd{sub 47-x}B{sub 6} (x=0.2, C2/m space group, a=1.03594(2) nm, b=1.80782(3) nm, c=1.01997(2) nm, beta=108.321(1){sup o}) was determined from Rietveld refinement of X-ray powder diffraction data applying the structural model obtained from single crystals of homologous La{sub 6}Pd{sub 47-x}B{sub 6} (x=0.19) (X-ray single crystal diffraction, new structure type, space group C2/m, a=1.03988(2) nm, b=1.81941(5) nm, c=1.02418(2) nm, beta=108.168(1){sup o}). The Yb-Pd-B system is characterized by one ternary compound, tau{sub 1}-Yb{sub 2}Pd{sub 14}B{sub 5}, forming equilibria with extended solution YbPd{sub 3}B{sub x}, YbB{sub 6}, Pd{sub 5}B{sub 2} and Pd{sub 3}B. The crystal structures of both Yb{sub 2}Pd{sub 14}B{sub 5} and isotypic Lu{sub 2}Pd{sub 14}B{sub 5} were determined from X-ray Rietveld refinements and found to be closely related to the Y{sub 2}Pd{sub 14}B{sub 5}-type (I4{sub 1}/amd). The crystal structure of binary Yb{sub 5}Pd{sub 2-x} (Mn{sub 5}C{sub 2}-type) was confirmed from X-ray single crystal data and a slight defect on the Pd site (x=0.06) was established. The three structures tau{sub 1}-Ce{sub 6}Pd{sub 47-x}B{sub 6}, tau{sub 2}-CePd{sub 8}B{sub 2-x} and tau{sub 3}-Ce{sub 3}Pd{sub 25-x}B{sub 8-y} are related and can be considered as the packings of fragments observed in Nd{sub 2}Fe{sub 14}B structure with different stacking of common structural blocks. Physical properties for Yb{sub 2}Pd{sub 13.6}B{sub 5} (temperature dependent specific heat, electrical resistivity and magnetization) yielded a predominantly Yb-4f{sup 13} electronic configuration, presumably related with a magnetic instability below 2 K. Kondo interaction and crystalline electric field effects control the paramagnetic temperature domain. - Graphical Abstract: Crystal structure of CePd{sub 8}B{sub 2-x}.

  10. Report for Treating Hanford LAW and WTP SW Simulants: Pilot Plant Mineralizing Flowsheet

    SciTech Connect (OSTI)

    Arlin Olson

    2012-02-28

    The US Department of Energy is responsible for managing the disposal of radioactive liquid waste in underground storage tanks at the Hanford site in Washington State. The Hanford waste treatment and immobilization plant (WPT) will separate the waste into a small volume of high level waste (HLW), containing most of the radioactive constituents, and a larger volume of low activity waste (LAW), containing most of the non-radioactive chemical and hazardous constituents. The HLW and LAW will be converted into immobilized waste forms for disposal. Currently there is inadequate LAW vitrification capacity planned at the WTP to complete the mission within the required timeframe. Therefore additional LAW capacity is required. One candidate supplemental treatment technology is the fluidized bed steam reformer process (FBSR). This report describes the demonstration testing of the FBSR process using a mineralizing flowsheet for treating simulated Hanford LAW and secondary waste from the WTP (WTP SW). The FBSR testing project produced leach-resistant solid products and environmentally compliant gaseous effluents. The solid products incorporated normally soluble ions into an alkali alumino-silicate (NaS) mineral matrix. Gaseous emissions were found to be within regulatory limits. Cesium and rhenium were captured in the mineralized products with system removal efficiencies of 99.999% and 99.998 respectively. The durability and leach performance of the FBSR granular solid were superior to the low activity reference material (LMR) glass standards. Normalized product consistency test (PCT) release rates for constituents of concern were approximately 2 orders of magnitude less than that of sodium in the Hanford glass [standard].

  11. Modeling the global emission, transport and deposition of trace elements associated with mineral dust

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Zhang, Y.; Mahowald, N.; Scanza, R.; Journet, E.; Desboeufs, K.; Albani, S.; Kok, J.; Zhuang, G.; Chen, Y.; Cohen, D. D.; et al

    2014-12-17

    Trace element deposition from desert dust has important impacts on ocean primary productivity. In this study, emission inventories for 8 elements, which are primarily of soil origin, Mg, P, Ca, Mn, Fe, K, Al, and Si were determined based on a global mineral dataset and a soils dataset. Datasets of elemental fractions were used to drive the desert dust model in the Community Earth System Model (CESM) in order to simulate the elemental concentrations of atmospheric dust. Spatial variability of mineral dust elemental fractions was evident on a global scale, particularly for Ca. Simulations of global variations in the Camore » / Al ratio, which typically ranged from around 0.1 to 5.0 in soil sources, were consistent with observations, suggesting this ratio to be a good signature for dust source regions. The simulated variable fractions of chemical elements are sufficiently different that estimates of deposition should include elemental variations, especially for Ca, Al and Fe. The model results have been evaluated with observational elemental aerosol concentration data from desert regions and dust events in non-dust regions, providing insights into uncertainties in the modeling approach. The ratios between modeled and observed elemental fractions ranged from 0.7 to 1.6 except for 3.4 and 3.5 for Mg and Mn, respectivly. Using the soil data base improved the correspondence of the spatial hetereogeneity in the modeling of several elements (Ca, Al and Fe) compared to observations. Total and soluble dust associated element fluxes into different ocean basins and ice sheets regions have been estimated, based on the model results. Annual inputs of soluble Mg, P, Ca, Mn, Fe and K associated with dust using mineral dataset were 0.28 Tg, 16.89 Gg, 1.32 Tg, 22.84 Gg, 0.068 Tg, and 0.15 Tg to global oceans and ice sheets.« less

  12. Mineral resources of the North Algodones Dunes Wilderness Study Area (CDCA-360), Imperial County, California

    SciTech Connect (OSTI)

    Smith, R.S.U.; Yeend, W.; Dohrenwend, J.C.; Gese, D.D.

    1984-01-01

    This report presents the results of a mineral survey of the North Algodones Dunes Wilderness Study Area (CDCA-360), California Desert Conservation Area, Imperial County, California. The potential for undiscovered base and precious metals, and sand and gravel within the North Algodones Dunes Wilderness Study Area is low. The study area has a moderate potential for geothermal energy. One small sand-free area between the Coachella Canal and the west edge of the dune field would probably be the only feasible exploration site for geothermal energy. The study area has a moderate to high potential for the occurrence of undiscovered gas/condensate within the underlying rocks. 21 refs.

  13. Calibrating the ChemCam LIBS for carbonate minerals on Mars

    SciTech Connect (OSTI)

    Wiens, Roger C; Clegg, Samuel M; Ollila, Ann M; Barefield, James E; Lanza, Nina; Newsom, Horton E

    2009-01-01

    The ChemCam instrument suite on board the NASA Mars Science Laboratory (MSL) rover includes the first LIBS instrument for extraterrestrial applications. Here we examine carbonate minerals in a simulated martian environment using the LIDS technique in order to better understand the in situ signature of these materials on Mars. Both chemical composition and rock type are determined using multivariate analysis (MVA) techniques. Composition is confirmed using scanning electron microscopy (SEM) techniques. Our initial results suggest that ChemCam can recognize and differentiate between carbonate materials on Mars.

  14. Pseudophasic extraction method for the separation of ultra-fine minerals

    DOE Patents [OSTI]

    Chaiko, David J. (Naperville, IL)

    2002-01-01

    An improved aqueous-based extraction method for the separation and recovery of ultra-fine mineral particles. The process operates within the pseudophase region of the conventional aqueous biphasic extraction system where a low-molecular-weight, water soluble polymer alone is used in combination with a salt and operates within the pseudo-biphase regime of the conventional aqueous biphasic extraction system. A combination of low molecular weight, mutually immiscible polymers are used with or without a salt. This method is especially suited for the purification of clays that are useful as rheological control agents and for the preparation of nanocomposites.

  15. Calibrating the ChemCam LIBS for Carbonate Minerals on Mars

    DOE R&D Accomplishments [OSTI]

    Wiens, Roger C.; Clegg, Samuel M.; Ollila, Ann M.; Barefield, James E.; Lanza, Nina; Newsom, Horton E.

    2009-01-01

    The ChemCam instrument suite on board the NASA Mars Science Laboratory (MSL) rover includes the first LIBS instrument for extraterrestrial applications. Here we examine carbonate minerals in a simulated martian environment using the LIDS technique in order to better understand the in situ signature of these materials on Mars. Both chemical composition and rock type are determined using multivariate analysis (MVA) techniques. Composition is confirmed using scanning electron microscopy (SEM) techniques. Our initial results suggest that ChemCam can recognize and differentiate between carbonate materials on Mars.

  16. Integrated Experimental and Modeling Studies of Mineral Carbonation as a Mechanism for Permanent Carbon Sequestration in Mafic/Ultramafic Rocks

    SciTech Connect (OSTI)

    Wang, Zhengrong; Qiu, Lin; Zhang, Shuang; Bolton, Edward; Bercovici, David; Ague, Jay; Karato, Shun-Ichiro; Oristaglio, Michael; Zhu, Wen-Iu; Lisabeth, Harry; Johnson, Kevin

    2014-09-30

    A program of laboratory experiments, modeling and fieldwork was carried out at Yale University, University of Maryland, and University of Hawaii, under a DOE Award (DE-FE0004375) to study mineral carbonation as a practical method of geologic carbon sequestration. Mineral carbonation, also called carbon mineralization, is the conversion of (fluid) carbon dioxide into (solid) carbonate minerals in rocks, by way of naturally occurring chemical reactions. Mafic and ultramafic rocks, such as volcanic basalt, are natural candidates for carbonation, because the magnesium and iron silicate minerals in these rocks react with brines of dissolved carbon dioxide to form carbonate minerals. By trapping carbon dioxide (CO2) underground as a constituent of solid rock, carbonation of natural basalt formations would be a secure method of sequestering CO2 captured at power plants in efforts to mitigate climate change. Geochemical laboratory experiments at Yale, carried out in a batch reactor at 200C and 150 bar (15 MPa), studied carbonation of the olivine mineral forsterite (Mg2SiO4) reacting with CO2 brines in the form of sodium bicarbonate (NaHCO3) solutions. The main carbonation product in these reactions is the carbonate mineral magnesite (MgCO3). A series of 32 runs varied the reaction time, the reactive surface area of olivine grains and powders, the concentration of the reacting fluid, and the starting ratio of fluid to olivine mass. These experiments were the first to study the rate of olivine carbonation under passive conditions approaching equilibrium. The results show that, in a simple batch reaction, olivine carbonation is fastest during the first 24 hours and then slows significantly and even reverses. A natural measure of the extent of carbonation is a quantity called the carbonation fraction, which compares the amount of carbon removed from solution, during a run, to the maximum amount that could have been removed if the olivine initially present had fully dissolved and the cations released had subsequently precipitated in carbonate minerals. The carbonation fractions observed in batch experiments with olivine grains and powders varied significantly, from less than 0.01 (1%) to more than 0.5 (50%). Over time, the carbonation fractions reached an upper limit after about 24 to 72 hours of reaction, then stayed constant or decreased. The peak Final Scientific/Technical Report DE-FE0004275 | Mineral Carbonation | 4 coincided with the appearance of secondary magnesium-bearing silicate minerals, whose formation competes for magnesium ions in solution and can even promote conditions that dissolve magnesite. The highest carbonation fractions resulted from experiments with low ratios of concentrated solution to olivine, during which amorphous silica spheres or meshes formed, instead of secondary silicate minerals. The highest carbonation fractions appear to result from competing effects. Precipitation of silica layers on olivine reduces the reactive surface area and, thus, the rate of olivine dissolution (which ultimately limits the carbonation rate), but these same silica layers can also inhibit the formation of secondary silicate minerals that consume magnesite formed in earlier stages of carbonation. Simulation of these experiments with simple geochemical models using the software program EQ3/6 reproduces the general trends observedespecially the results for the carbonation fraction in short-run experiments. Although further experimentation and better models are needed, this study nevertheless provides a framework for understanding the optimal conditions for sequestering carbon dioxide by reacting CO2-bearing fluids with rocks containing olivine minerals. A series of experiments at the Rock Physics Laboratory at the University of Maryland studied the carbonation process during deformation of thermally cracked olivine-rich rock samples (dunit

  17. Evidence for an unsaturated-zone origin of secondary minerals in Yucca Mountain, Nevada

    SciTech Connect (OSTI)

    Whelan, Joseph F.; Roedder, Edwin; Paces, James B.

    2001-04-29

    The unsaturated zone (UZ) in Miocene-age welded tuffs at Yucca Mountain, Nevada, is under consideration as a potential site for the construction of a high-level radioactive waste repository. Secondary calcite and silica minerals deposited on fractures and in cavities in the UZ tuffs are texturally, isotopically, and geochemically consistent with UZ deposition from meteoric water infiltrating at the surface and percolating through the UZ along fractures. Nonetheless, two-phase fluid inclusions with small and consistent vapor to liquid (V:L) ratios that yield consistent temperatures within samples and which range from about 35 to about 80 C between samples have led some to attribute these deposits to formation from upwelling hydrothermal waters. Geochronologic studies have shown that calcite and silica minerals began forming at least 10 Ma and continued to form into the Holocene. If their deposition were really from upwelling water flooding the UZ, it would draw into question the suitability of the site as a waste repository.

  18. Stable isotopes of authigenic minerals in variably-saturated fractured tuff

    SciTech Connect (OSTI)

    Weber, D.S.; Evans, D.D.

    1988-11-01

    Identifying stable isotope variation and mineralogical changes in fractured rock may help establish the history of climatic and geomorphological processes that might affect the isolation properties of a waste repository site. This study examines the use of the stable isotope ratios of oxygen ({sup 18}O/{sup 16}O) and carbon ({sup 13}C/{sup 12}C) in authigenic minerals as hydrogeochemical tools tracing low-temperature rock-water interaction in variably-saturated fractured stuff. Isotopic compositions of fracture-filling and rock matrix minerals in the Apache Leap tuff, near Superior, Arizona were concordant with geothermal temperatures and in equilibrium with water isotopically similar to present-day meteoric water and groundwater. Oxygen and carbon isotope ratios of fracture-filling, in unsaturated fractured tuff, displayed an isotopic gradient believed to result from near-surface isotopic enrichment due to evaporation rather than the effects of rock-water interaction. Oxygen isotope ratios of rock matrix opal samples exhibited an isotopic gradient believed to result from, leaching and reprecipitation of silica at depth. Methods and results can be used to further define primary flowpaths and the movement of water in variably-saturated fractured rock. 71 refs., 23 figs., 3 tabs.

  19. Defending mining claims and mineral leases in environmental suits against federal land managers

    SciTech Connect (OSTI)

    Twelker, E. )

    1989-01-01

    Suits in the last 4-5 years jeopardize the title of thousands of mining claims and mineral leases. The cases presenting the most striking examples are National Wildlife Federation v. Burford, Connor v. Burford, Sierra Club V. Watt, and Bob Marshall Alliance v. Watt. From the claimants' and lessees' point of view, these decisions granted environmental groups sweeping, though somewhat ill-defined, relief. The challenges by environmental groups are based on statutes designed to bring environmental considerations before federal decision makers. The claimants and lessees are caught in the middle of the exchange between environmentalists and federal agencies. Lawsuits that indirectly challenge leases and claims are unlike environmental challenges to fixed projects such as highways or dams. Those affected often times do not know exactly what is at stake. When the challenge is indirect, unexplored, or partially explored, proper ties have only speculative value and the claimants and lessees are often unwilling or unable to engage in a fight with well-heeled environmental public interest law firms. While the federal government has defended the suits, their interests and those of the claimants and lessees may diverge. In the context of the four cases mentioned above, this paper addresses the rights and remedies of claimants and lessees before, during, and after environmental procedural suits that indirectly challenge federal mining claims and mineral leases.

  20. Identification of concrete deteriorating minerals by polarizing and scanning electron microscopy

    SciTech Connect (OSTI)

    Gregerova, Miroslava; Vsiansky, Dalibor

    2009-07-15

    The deterioration of concrete represents one of the most serious problems of civil engineering worldwide. Besides other processes, deterioration of concrete consists of sulfate attack and carbonation. Sulfate attack results in the formation of gypsum, ettringite and thaumasite in hardened concrete. Products of sulfate attack may cause a loss of material strength and a risk of collapse of the concrete constructions. The authors focused especially on the microscopical research of sulfate attack. Concrete samples were taken from the Charles Bridge in Prague, Czech Republic. A succession of degrading mineral formation was suggested. Microscope methods represent a new approach to solving the deterioration problems. They enable evaluation of the state of concrete constructions and in cooperation with hydro-geochemistry, mathematics and statistics permit prediction of the durability of a structure. Considering the number of concrete constructions and their age, research of concrete deterioration has an increasing importance. The results obtained can also be useful for future construction, because they identify the risk factors associated with formation of minerals known to degrade structures.

  1. Chemical analyses of rocks, minerals, and detritus, Yucca Mountain--Preliminary report, special report No. 11

    SciTech Connect (OSTI)

    Hill, C.A.; Livingston, D.E.

    1993-09-01

    This chemical analysis study is part of the research program of the Yucca Mountain Project intended to provide the State of Nevada with a detailed assessment of the geology and geochemistry of Yucca Mountain and adjacent regions. This report is preliminary in the sense that more chemical analyses may be needed in the future and also in the sense that these chemical analyses should be considered as a small part of a much larger geological data base. The interpretations discussed herein may be modified as that larger data base is examined and established. All of the chemical analyses performed to date are shown in Table 1. There are three parts to this table: (1) trace element analyses on rocks (limestone and tuff) and minerals (calcite/opal), (2) rare earth analyses on rocks (tuff) and minerals (calcite/opal), and (3) major element analyses + CO{sub 2} on rocks (tuff) and detritus sand. In this report, for each of the three parts of the table, the data and its possible significance will be discussed first, then some overall conclusions will be made, and finally some recommendations for future work will be offered.

  2. Magnetic hardening of Ce1+xFe11yCoyTi with ThMn12 structure by melt spinning

    SciTech Connect (OSTI)

    Zhou, Chen; Sun, Kewei; Pinkerton, Frederick E.; Kramer, M. J.

    2015-04-15

    A recent study on the intrinsic magnetic properties of CeFe11yCoyTi has revealed that substituting one Co for Fe retains the favorable magnetocrystalline anisotropy Ha found in the ternary Fe end member, while enhancing the Curie temperature Tc and saturation magnetization 4?Ms. These findings warrant further optimization around Co substitution y = 1 to try to exploit the hard magnetic properties of these Ce-based magnets. Both Ce and Co concentrations in Ce1+xFe11yCoyTi have been optimized in the range of x = 0 0.2 and y = 0 1.5. It was found that Co substitution effectively enhances all hard magnetic properties, although the values are still lower than those predicted from the intrinsic magnetic properties. Specifically, Tc increases from 210 C to 285 350 C; 4?M19 (magnetization at 19 kOe) from 8.9 kG to 10.5 11.5 kG, remanence Br from 3.1 kG to 4.1 4.5 kG, and most importantly, Hci from 1.1 kOe to 1.5 kOe. As a result, the room temperature energy product (BH)max has been increased by over 100% from 0.7 MGOe in Ce1.1Fe11Ti to 1.5 MGOe in Ce1.05Fe9.75Co1.25Ti. Microscopy analysis indicates that the addition of Co refines the grain size and promotes chemical homogeneity at the microscopic scale. As a result, the beneficial effect of Co on the microstructure contributes to the improved hard magnetic properties.

  3. Associations of symptoms related to isocyanate, ureaformol, and formophenolic exposures with respiratory symptoms and lung function in coal miners

    SciTech Connect (OSTI)

    Bertrand, J.P.; Simon, V.; Chau, N.

    2007-04-15

    The respiratory effects of diphenylmethane diisocyanate (MDI)-based resins and ureaformol- and formophenolic-based resins, used in coal mining, are unknown. This cross-sectional study of 354 miners evaluated respiratory health in miners with MDI-related symptoms (IS) and ureaformol/formophenolic-related symptoms (UFS). The protocol included clinical examination, chest radiograph, questionnaire on respiratory symptoms, smoking habit, job history, resin handling, and spirometry. Resin handling concerned 27.7% of the miners. IS affected 5.6%, and 1.4% also after work. UFS affected 22.6%, and 2.3% also after work. Wheezing affected 35.6%; chronic cough, expectoration, or bronchitis about 10%; dyspnea 5.4%; and asthma 2.8%. The miners with UFS had significantly more frequent chronic cough, expectoration, chronic bronchitis, dyspnea, and wheezing, whereas those with IS at and after work had markedly lower FVC, FEV1, MMEF, FEF50% and FEF25%. These findings raise the possibility of deleterious effects of exposures to MDI and ureaformol/ ormophenolic resins on respiratory health and lung function in coal miners during their working life.

  4. Performance of Ni-Fe/gadolinium-doped CeO{sub2} anode supported tubular solid oxide fuel cells using steam reforming of methane

    SciTech Connect (OSTI)

    Liang, B.; Suzuki, T.; Hamamoto, K.; Yamaguchi, T.; Sumi, H.; Fujishiro, Y.; Ingram, B. J.; Carter, J. D.

    2012-03-15

    Iron nanoparticles (Fe{sub 2}O{sub 3}) were added to NiO/gadolinium-doped CeO{sub 2} (GDC) anode supported solid oxide fuel cell (SOFC) for the direct methane-water fuel operation. The cell was co-sintered at 1400 C, and the anode porosity is 31.8%. The main size corresponding to peak volume is around 1.5 {mu}m. When steam and methane directly fed to the cell, the power density is about 0.57 W cm{sup -2} at 650 C. It is the familiar performance for H{sub 2} operation (4 times of flow rate) with same fuel utilization. Compare with the testing temperature of 600 and 650 C, there is almost no carbon fiber deposition at 700 C with steam/methane (S/C) of 5. At the same time, fuel operation of high value of S/C (=3.3) resulted in fiber-like deposition and degradation of power performance based on loading test results.

  5. An In-Situ XAS Study of the Structural Changes in a CuO-CeO2/Al2O3 Catalyst during Total Oxidation of Propane

    SciTech Connect (OSTI)

    Silversmith, Geert; Poelman, Hilde; Poelman, Dirk; Gryse, Roger de; Olea, Maria; Balcaen, Veerle; Heynderickx, Philippe; Marin, Guy B.

    2007-02-02

    A CuOx-CeOx/Al2O3 catalyst was studied with in-situ transmission Cu K XAS for the total oxidation of propane as model reaction for the catalytic elimination of volatile organic compounds. The local Cu structure was determined for the catalyst as such, after pre-oxidation and after reduction with propane. The catalyst as such has a local CuO structure. No structural effect was observed upon heating in He up to 600 deg. C or after pre-oxidation at 150 deg. C. A full reduction of the Cu2+ towards metallic Cu0 occurred, when propane was fed to the catalyst. The change in local Cu structure during propane reduction was followed with a time resolution of 1 min. The {chi}(k) scans appeared as linear combinations of start and end spectra, CuO and Cu structure, respectively. However, careful examination of the XANES edge spectra indicates the presence of a small amount of additional Cu1+ species.

  6. Effect of 8 MeV electron beam irradiation on the structural and optical properties of CeO{sub 2} nanoparticles

    SciTech Connect (OSTI)

    Babitha, K.K.; Priyanka, K.P.; Sreedevi, A.; Ganesh, S.; Varghese, Thomas

    2014-12-15

    The effect of 8 MeV electron beam irradiation on the structural and optical properties of cerium oxide nanoparticles was investigated. Ceria nanoparticles were synthesized by chemical precipitation method, and characterized by X-ray diffraction, transmission electron microscopy, ultravioletvisible, photoluminescence and Raman spectroscopy. Ultravioletvisible absorption spectra, photoluminescence and Raman spectra of beam irradiated samples were modified, and shifted to blue region, which were attributed to quantum size effect. Systematic observations found that nonstoichiometry, defects and size reduction caused by beam irradiation have great influence on optical band gap, blue shift, photoluminescence and Raman band modifications. Moreover, electron beam irradiation is a suitable technique to enhance the structural and optical properties of nanoceria by controlling the particle size, which may lead to potentially useful technological applications. - Highlights: Investigated effect of beam irradiation on CeO{sub 2} nanoparticles Beam irradiation caused size reduction and surface modification. It increases microstrain, decreases d-spacing and broadens XRD peaks. It also modifies optical band gap, absorption, PL and Raman bands.

  7. Splitting of the pygmy dipole resonance in {sup 138}Ba and {sup 140}Ce observed in the ({alpha},{alpha}{sup '}{gamma}) reaction

    SciTech Connect (OSTI)

    Endres, J.; Hasper, J.; Zilges, A.; Savran, D.; Berg, A. M. van den; Dendooven, P.; Woertche, H. J.; Fritzsche, M.; Harakeh, M. N.

    2009-09-15

    The N=82 nuclei {sup 140}Ce and {sup 138}Ba have been investigated by means of the ({alpha},{alpha}{sup '}{gamma}) coincidence method to study the pygmy dipole resonance (PDR). The experiments have been performed at the AGOR cyclotron at KVI, Groningen, at a primary beam energy of E{sub {alpha}}=136 MeV. The Big-Bite Spectrometer and seven large-volume high-purity germanium detectors were used in coincidence to perform a simultaneous spectroscopy of the scattered {alpha} particles and the {gamma} decay. The comparison with results of nuclear resonance fluorescence experiments reveals a splitting of the PDR into two components. Up to about 6 MeV the same states that could be observed in ({gamma},{gamma}{sup '}) are also excited in {alpha}-scattering experiments, whereas the higher-lying states are missing in the ({alpha},{alpha}{sup '}{gamma}) reaction. This indicates a structural splitting of the PDR into two modes with different underlying structure.

  8. Fluidized Bed Steam Reforming of Hanford LAW Using THORsm Mineralizing Technology

    SciTech Connect (OSTI)

    Olson, Arlin L.; Nicholas R Soelberg; Douglas W. Marshall; Gary L. Anderson

    2004-11-01

    The U.S. Department of Energy (DOE) documented, in 2002, a plan for accelerating cleanup of the Hanford Site, located in southeastern Washington State, by at least 35 years. A key element of the plan was acceleration of the tank waste program and completion of ''tank waste treatment by 2028 by increasing the capacity of the planned Waste Treatment Plant (WTP) and using supplemental technologies for waste treatment and immobilization.'' The plan identified steam reforming technology as a candidate for supplemental treatment of as much as 70% of the low-activity waste (LAW). Mineralizing steam reforming technology, offered by THOR Treatment Technologies, LLC would produce a denitrated, granular mineral waste form using a high-temperature fluidized bed process. A pilot scale demonstration of the technology was completed in a 15-cm-diameter reactor vessel. The pilot scale facility was equipped with a highly efficient cyclone separator and heated sintered metal filters for particulate removal, a thermal oxidizer for reduced gas species and NOx destruction, and a packed activated carbon bed for residual volatile species capture. The pilot scale equipment is owned by the DOE, but located at the Science and Technology Applications Research (STAR) Center in Idaho Falls, ID. Pilot scale testing was performed August 25, 2004. Flowsheet chemistry and operational parameters were defined through a collaborative effort involving Idaho National Engineering and Environmental Laboratory, Savannah River National Laboratory (SRNL), and THOR Treatment Technologies personnel. Science Application International Corporation, owners of the STAR Center, personnel performed actual pilot scale operation. The pilot scale test achieved a total of 68.7 hrs of cumulative/continuous processing operation before termination in response to a bed de-fluidization condition. 178 kg of LAW surrogate were processed that resulted in 148 kg of solid product, a mass reduction of about 17%. The process achieved essentially complete bed turnover within approximately 40 hours. Samples of mineralized solid product materials were analyzed for chemical/physical properties. SRNL will report separately the results of product performance testing that were accomplished.

  9. The Origin of Refractory Minerals in Comet 81P/Wild 2

    SciTech Connect (OSTI)

    Chi, M; Ishii, H A; Simon, S B; Bradley, J P; Dai, Z R; Joswiak, D J; Browning, N D; Matrajt, G

    2008-11-20

    Refractory Ti-bearing minerals in the calcium-, aluminium-rich inclusion (CAI) Inti, recovered from the comet 81P/Wild 2 sample, were examined using analytical (scanning) transmission electron microscopy (STEM) methods including imaging, nanodiffraction, energy dispersive spectroscopy (EDX) and electron energy loss spectroscopy (EELS). Inti fassaite (Ca(Mg,Ti,Al)(Si,Al){sub 2}O{sub 6}) was found to have a Ti{sup 3+}/Ti{sup 4+} ratio of 2.0 {+-} 0.2, consistent with fassaite in other solar system CAIs. The oxygen fugacity (log f{sub O{sub 2}}) of formation estimated from this ratio, assuming equilibration among phases at 1509K, is -19.4 {+-} 1.3. This value is near the canonical solar nebula value (-18.1 {+-} 0.3) and in close agreement with that reported for fassaite-bearing Allende CAIs (-19.8 {+-} 0.9) by other researchers using the same assumptions. Nanocrystals of osbornite (Ti(V)N), 2-40 nm in diameter, are embedded as inclusions within anorthite, spinel and diopside in Inti. Vanadium is heterogeneously distributed within some osbornite crystals. Compositions range from pure TiN to Ti{sub 0.36}V{sub 0.64}N. The possible presence of oxide and carbide in solid solution with the osbornite was evaluated. The osbornite may contain O but does not contain C. The presence of osbornite, likely a refractory early condensate, together with the other refractory minerals in Inti, indicates that the parent comet contains solids that condensed closer to the proto-sun than the distance at which the parent comet itself accreted. The estimated oxygen fugacity and the reported isotopic and chemical compositions are consistent with Inti originating in the inner solar system as opposed to it being a surviving CAI from an extrasolar source. These results provide insight for evaluating the validity of models of radial mass transport dynamics in the early solar system. The oxidation environments inferred for the Inti mineral assemblage are inconsistent with an X-wind formation scenario. In contrast, radial mixing models allowing accretion of components from different heliocentric distances can satisfy the observations from the cometary CAI Inti.

  10. Fluidized Bed Steam Reforming of INEEL SBW Using THORsm Mineralizing Technology

    SciTech Connect (OSTI)

    Arlin L. Olson; Nicholas R. Soelberg; Douglas W. Marshall; Gary L. Anderson

    2004-12-01

    Sodium bearing waste (SBW) disposition is one of the U.S. Department of Energy (DOE) Idaho Operation Offices (NE-ID) and State of Idahos top priorities at the Idaho National Engineering and Environmental Laboratory (INEEL). Many studies have resulted in the identification of five treatment alternatives that form a short list of perhaps the most appropriate technologies for the DOE to select from. The alternatives are (a) calcination with maximum achievable control technology (MACT) upgrade, (b) steam reforming, (c) cesium ion exchange (CsIX) with immobilization, (d) direct evaporation, and (e) vitrification. Each alternative has undergone some degree of applied technical development and preliminary process design over the past four years. DOE desired further experimental data, with regard to steam reforming technology, to make informed decisions concerning selection of treatment technology for SBW. Mineralizing steam reforming technology, offered by THOR Treatment Technologies, LLC would produce a denitrated, granular mineral waste form using a high-temperature fluidized bed process. A pilot scale demonstration of the technology was performed in a 15-cm-diameter reactor vessel September 27 through October 1, 2004. The pilot scale equipment is owned by the DOE, and located at the Science and Technology Applications Research (STAR) Center in Idaho Falls, ID. Flowsheet chemistry and operational parameters were defined through a collaborative effort involving Idaho National Engineering and Environmental Laboratory, Savannah River National Laboratory (SRNL), and THOR Treatment Technologies personnel. Personnel from Science Applications International Corporation, owners of the STAR Center, operated the pilot plant. The pilot scale test was terminated as planned after achieving a total of 100 hrs of cumulative/continuous processing operation. About 230 kg of SBW surrogate were processed that resulted in about 88 kg of solid product, a mass reduction of about 62%. The process achieved about a 90% turnover of the starting bed. Samples of mineralized solid product materials were analyzed for chemical/physical properties. Results of product performance testing conducted by SRNL will be reported separately by SRNL.

  11. Modeling the global emission, transport and deposition of trace elements associated with mineral dust

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Zhang, Y.; Mahowald, N.; Scanza, R. A.; Journet, E.; Desboeufs, K.; Albani, S.; Kok, J. F.; Zhuang, G.; Chen, Y.; Cohen, D. D.; et al

    2015-10-12

    Trace element deposition from desert dust has important impacts on ocean primary productivity, the quantification of which could be useful in determining the magnitude and sign of the biogeochemical feedback on radiative forcing. However, the impact of elemental deposition to remote ocean regions is not well understood and is not currently included in global climate models. In this study, emission inventories for eight elements primarily of soil origin, Mg, P, Ca, Mn, Fe, K, Al, and Si are determined based on a global mineral data set and a soil data set. The resulting elemental fractions are used to drive themore » desert dust model in the Community Earth System Model (CESM) in order to simulate the elemental concentrations of atmospheric dust. Spatial variability of mineral dust elemental fractions is evident on a global scale, particularly for Ca. Simulations of global variations in the Ca / Al ratio, which typically range from around 0.1 to 5.0 in soils, are consistent with observations, suggesting that this ratio is a good signature for dust source regions. The simulated variable fractions of chemical elements are sufficiently different; estimates of deposition should include elemental variations, especially for Ca, Al and Fe. The model results have been evaluated with observations of elemental aerosol concentrations from desert regions and dust events in non-dust regions, providing insights into uncertainties in the modeling approach. The ratios between modeled and observed elemental fractions range from 0.7 to 1.6, except for Mg and Mn (3.4 and 3.5, respectively). Using the soil database improves the correspondence of the spatial heterogeneity in the modeling of several elements (Ca, Al and Fe) compared to observations. Total and soluble dust element fluxes to different ocean basins and ice sheet regions have been estimated, based on the model results. The annual inputs of soluble Mg, P, Ca, Mn, Fe and K associated with dust using the mineral data set are 0.30 Tg, 16.89 Gg, 1.32 Tg, 22.84 Gg, 0.068 Tg, and 0.15 Tg to global oceans and ice sheets.« less

  12. Strain-guided mineralization in the bone–PDL–cementum complex of a rat periodontium

    SciTech Connect (OSTI)

    Grandfield, Kathryn; Herber, Ralf -Peter; Chen, Ling; Djomehri, Sabra; Tam, Caleb; Lee, Ji -Hyun; Brown, Evan; Woolwine III, Wood R.; Curtis, Don; Ryder, Mark; Schuck, Jim; Webb, Samuel; Landis, William; Ho, Sunita P.

    2015-04-18

    Objective: The objective of this study was to investigate the effect of mechanical strain by mapping physicochemical properties at periodontal ligament (PDL)–bone and PDL–cementum attachment sites and within the tissues per se. Design: Accentuated mechanical strain was induced by applying a unidirectional force of 0.06 N for 14 days on molars in a rat model. The associated changes in functional space between the tooth and bone, mineral forming and resorbing events at the PDL–bone and PDL–cementum attachment sites were identified by using micro-X-ray computed tomography (micro-XCT), atomic force microscopy (AFM), dynamic histomorphometry, Raman microspectroscopy, and AFM-based nanoindentation technique. Results from these analytical techniques were correlated with histochemical strains specific to low and high molecular weight GAGs, including biglycan, and osteoclast distribution through tartrate resistant acid phosphatase (TRAP) staining. Results: Unique chemical and mechanical qualities including heterogeneous bony fingers with hygroscopic Sharpey's fibers contributing to a higher organic (amide III — 1240 cm⁻¹) to inorganic (phosphate — 960 cm⁻¹) ratio, with lower average elastic modulus of 8 GPa versus 12 GPa in unadapted regions were identified. Furthermore, an increased presence of elemental Zn in cement lines and mineralizing fronts of PDL–bone was observed. Adapted regions containing bony fingers exhibited woven bone-like architecture and these regions rich in biglycan (BGN) and bone sialoprotein (BSP) also contained high-molecular weight polysaccharides predominantly at the site of polarized bone growth. Conclusions: From a fundamental science perspective the shift in local properties due to strain amplification at the soft–hard tissue attachment sites is governed by semiautonomous cellular events at the PDL–bone and PDL–cementum sites. Over time, these strain-mediated events can alter the physicochemical properties of tissues per se, and consequently the overall biomechanics of the bone–PDL–tooth complex. From a clinical perspective, the shifts in magnitude and duration of forces on the periodontal ligament can prompt a shift in physiologic mineral apposition in cementum and alveolar bone albeit of an adapted quality owing to the rapid mechanical translation of the tooth.

  13. Strain-guided mineralization in the bone–PDL–cementum complex of a rat periodontium

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Grandfield, Kathryn; Herber, Ralf -Peter; Chen, Ling; Djomehri, Sabra; Tam, Caleb; Lee, Ji -Hyun; Brown, Evan; Woolwine III, Wood R.; Curtis, Don; Ryder, Mark; et al

    2015-04-18

    Objective: The objective of this study was to investigate the effect of mechanical strain by mapping physicochemical properties at periodontal ligament (PDL)–bone and PDL–cementum attachment sites and within the tissues per se. Design: Accentuated mechanical strain was induced by applying a unidirectional force of 0.06 N for 14 days on molars in a rat model. The associated changes in functional space between the tooth and bone, mineral forming and resorbing events at the PDL–bone and PDL–cementum attachment sites were identified by using micro-X-ray computed tomography (micro-XCT), atomic force microscopy (AFM), dynamic histomorphometry, Raman microspectroscopy, and AFM-based nanoindentation technique. Results frommore » these analytical techniques were correlated with histochemical strains specific to low and high molecular weight GAGs, including biglycan, and osteoclast distribution through tartrate resistant acid phosphatase (TRAP) staining. Results: Unique chemical and mechanical qualities including heterogeneous bony fingers with hygroscopic Sharpey's fibers contributing to a higher organic (amide III — 1240 cm⁻¹) to inorganic (phosphate — 960 cm⁻¹) ratio, with lower average elastic modulus of 8 GPa versus 12 GPa in unadapted regions were identified. Furthermore, an increased presence of elemental Zn in cement lines and mineralizing fronts of PDL–bone was observed. Adapted regions containing bony fingers exhibited woven bone-like architecture and these regions rich in biglycan (BGN) and bone sialoprotein (BSP) also contained high-molecular weight polysaccharides predominantly at the site of polarized bone growth. Conclusions: From a fundamental science perspective the shift in local properties due to strain amplification at the soft–hard tissue attachment sites is governed by semiautonomous cellular events at the PDL–bone and PDL–cementum sites. Over time, these strain-mediated events can alter the physicochemical properties of tissues per se, and consequently the overall biomechanics of the bone–PDL–tooth complex. From a clinical perspective, the shifts in magnitude and duration of forces on the periodontal ligament can prompt a shift in physiologic mineral apposition in cementum and alveolar bone albeit of an adapted quality owing to the rapid mechanical translation of the tooth.« less

  14. Development of Advanced Surface Enhancement Technology for Decreasing Wear and Corrosion of Equipment Used for Mineral Processing

    SciTech Connect (OSTI)

    Daniel Tao; Craig A. Blue

    2004-08-01

    Equipment wear is a major concern in the mineral processing industry, which dramatically increases the maintenance cost and adversely affects plant operation efficiency. In this research, wear problems of mineral processing equipment including screens, sieve bends, heavy media vessel, dewatering centrifuge, etc., were identified. A novel surface treatment technology, high density infrared (HDI) surface coating process was proposed for the surface enhancement of selected mineral processing equipment. Microstructural and mechanical properties of the coated samples were characterized. Laboratory-simulated wear tests were conducted to evaluate the tribological performance of the coated components. Test results indicate that the wear resistance of AISI 4140 and ASTM A36 steels can be increased 3 and 5 folds, respectively by the application of HDI coatings.

  15. GaMin11 an international inter-laboratory comparison for geochemical CO? - saline fluid - mineral interaction experiments

    SciTech Connect (OSTI)

    Ostertag-Henning, C. [Federal Inst. for Geosciences and Natural Resesources (BGR), Hannover (Germany); Risse, A. [Federal Inst. for Geosciences and Natural Resesources (BGR), Hannover (Germany); Thomas, B. [United States Geological Survey, Menlo Park, CA (United States); Rosenbauer, R. [United States Geological Survey, Menlo Park, CA (United States); Rochelle, C. [British Geological Survey, Nottinghamshire (United Kingdom); Purser, G. [British Geological Survey, Nottinghamshire (United Kingdom); Kilpatrick, A. [British Geological Survey, Nottinghamshire (United Kingdom); Rosenqvist, J. [Univ. of Leeds (United Kingdom); Yardley, B. [Univ. of Leeds (United Kingdom); Karamalidis, A. [Carnegie Mellon Univ., Pittsburgh, PA (United States); Griffith, C. [National Energy Technology Lab., Pittsburgh, PA (United States); Hedges, S. [National Energy Technology Lab., Pittsburgh, PA (United States); Dilmore, R. [National Energy Technology Lab., Pittsburgh, PA (United States); Goodman, A. [National Energy Technology Lab., Pittsburgh, PA (United States); Black, J. [Univ. of Melbourne, (Austrialia); Haese, R. [Univ. of Melbourne, (Austrialia); Deusner, C. [hGEOMAR Helmholtz Center for Ocean Research, Kiel (Germany); Bigalke, N. [hGEOMAR Helmholtz Center for Ocean Research, Kiel (Germany); Haeckel, M. [hGEOMAR Helmholtz Center for Ocean Research, Kiel (Germany); Fischer, S. [GFZ German Research Centre for Geosciences, Potsdam (Germany); Liebscher, A. [GFZ German Research Centre for Geosciences, Potsdam (Germany); Icenhower, J. P. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Daval, D. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Saldi, G. D. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Knauss, K. G. [Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States); Schmidt, M. [Martin Luther Univ., Halle (Germany); Mito, S. [Research Inst. of Innovative Tech. for the Earth (RITE), Kyoto (Japan); Sorai, M. [National Inst. of Advanced Science and Tech. (AIST) Tsukuba (Japan); Truche, L. [GeoRessources, Universite de Lorraine, Nancy (France)

    2014-12-31

    Due to the strong interest in geochemical CO?-fluid-rock interaction in the context of geological storage of CO? a growing number of research groups have used a variety of different experimental ways to identify important geochemical dissolution or precipitation reactions and if possible quantify the rates and extent of mineral or rock alteration. In this inter-laboratory comparison the gas-fluid-mineral reactions of three samples of rock-forming minerals have been investigated by 11 experimental labs. The reported results point to robust identification of the major processes in the experiments by most groups. The dissolution rates derived from the changes in composition of the aqueous phase are consistent overall, but the variation could be reduced by using similar corrections for changing parameters in the reaction cells over time. The comparison of experimental setups and procedures as well as of data corrections identified potential improvements for future gas-fluid-rock studies.

  16. Crystal structure, magnetism and transport properties of Ce{sub 3}Ni{sub 25.75}Ru{sub 3.16}Al{sub 4.1}B{sub 10}

    SciTech Connect (OSTI)

    Janka, Oliver; Baumbach, Ryan E.; Thompson, Joe D.; Bauer, Eric D.; Kauzlarich, Susan M.

    2013-09-15

    Single crystals of Ce{sub 3}Ni{sub 25.75}Ru{sub 3.16}Al{sub 4.1}B{sub 10} were obtained from a process in which a polycrystalline sample of CeRu{sub 2}Al{sub 2}B was annealed in an excess of a NiIn flux. The initial phase, CeRu{sub 2}Al{sub 2}B, does not recrystallize, instead, crystals of a new phase, Ce{sub 3}Ni{sub 25.75}Ru{sub 3.16}Al{sub 4.1}B{sub 10}, could be isolated once the flux was removed. The title compound crystallizes in the tetragonal space group P4/nmm (No. 129) with a=1139.02(8), c=801.68(6) pm (c/a=0.70) in the Nd{sub 3}Ni{sub 29}Si{sub 4}B{sub 10} structure type. Electrical resistivity measurements reveal metallic behavior with a minimum of 700 ? cm and a small residual resistivity ratio of RRR=1.4 indicating a large amount of disorder scattering. The cerium atoms are either in the 4+ or an intermediate valence state with a valence fluctuation temperature far above room temperature. - Graphical abstract: Single crystals of Ce{sub 3}Ni{sub 25.75}Ru{sub 3.16}A{sub l4.1}B{sub 10} were obtained using a process in which a polycrystalline sample of CeRu{sub 2}Al{sub 2}B was annealed in an excess of a NiIn flux. Electrical resistivity measurements reveal metallic behavior with a minimum of 700 ?? cm and a small residual resistivity ratio of RRR=1.4 indicating a large amount of disorder scattering. The cerium atoms are either in the 4+ or an intermediate valence state with a valence fluctuation temperature far above room temperature. Display Omitted - Highlights: Flux synthesis of high quality single crystals of Ce{sub 3}Ni{sub 25.75}Ru{sub 3.16}Al{sub 4.1}B{sub 10} is presented along with the crystal structure, magnetic and transport properties. The compound is isostructural to Nd{sub 3}Ni{sub 29}Si{sub 4}B{sub 10} but is first of this structure type showing mixed occupancies of d-elements. This is an intermetallic phase with Ce in either the 4+ or an intermediate valence state. The fact that this structure with mixed occupied transition metal sites exists suggests that more compounds of this type should be accessible and the physical properties tuned.

  17. UFe/sub 4/P/sub 12/ and CeFe/sub 4/P/sub 12/: non-metallic isotypes of superconducting LaFe/sub 4/P/sub 12/

    SciTech Connect (OSTI)

    Meisner, G.P.; Torikachvili, M.S.; Yang, K.N.; Maple, M.B.; Guertin, R.P.

    1984-01-01

    The new compound UFe/sub 4/P/sub 12/, which was found to be isostructural to superconducting LaFe/sub 4/P/sub 12/ and with a lattive constant of 7.7729 A, is a semiconductor and shows ferromagnetic order below 3.15 K. CeFe/sub 4/P/sub 12/ is also a semiconductor and its magnetic susceptibility is unusually small in comparison to LaFe/sub 4/P/sub 12/. The semiconducting behaviors of both UFe/sub 4/P/sub 12/ and CeFe/sub 4/P/sub 12/ seem anomalous and may arise from strong f-electron hybridization.

  18. UFe/sub 4/P/sub 12/ and CeFe/sub 4/P/sub 12/: Nonmetallic isotypes of superconducting LaFe/sub 4/P/sub 12/

    SciTech Connect (OSTI)

    Meisner, G.P.; Torikachvili, M.S.; Yang, K.N.; Maple, M.B.; Guertin, R.P.

    1985-04-15

    The new compound UFe/sub 4/P/sub 12/, which was found to be isostructural to superconducting LaFe/sub 4/P/sub 12/ and have a lattice constant of 7.7729 A, is a semiconductor and shows ferromagnetic order below 3.15 K. CeFe/sub 4/P/sub 12/ is also a semiconductor, and its magnetic susceptibility is unusually small in comparison to LaFe/sub 4/P/sub 12/. The semiconducting behaviors of both UFe/sub 4/P/sub 12/ and CeFe/sub 4/P/sub 12/ seem anomalous and may arise from strong f-electron hybridization.

  19. Improvement of {gamma}-ray energy resolution of LaBr{sub 3}:Ce{sup 3+} scintillation detectors by Sr{sup 2+} and Ca{sup 2+} co-doping

    SciTech Connect (OSTI)

    Alekhin, M. S.; Haas, J. T. M. de; Khodyuk, I. V.; Dorenbos, P.; Kraemer, K. W.; Menge, P. R.; Ouspenski, V.

    2013-04-22

    Commercially available LaBr{sub 3}:5% Ce{sup 3+} scintillators show with photomultiplier tube readout about 2.7% energy resolution for the detection of 662 keV {gamma}-rays. Here we will show that by co-doping LaBr{sub 3}:Ce{sup 3+} with Sr{sup 2+} or Ca{sup 2+} the resolution is improved to 2.0%. Such an improvement is attributed to a strong reduction of the scintillation light losses that are due to radiationless recombination of free electrons and holes during the earliest stages (1-10 ps) inside the high free charge carrier density parts of the ionization track.

  20. Mineral dissolution and precipitation during CO2 injection at the Frio-I Brine Pilot: Geochemical modeling and uncertainty analysis

    DOE Public Access Gateway for Energy & Science Beta (PAGES Beta)

    Ilgen, A. G.; Cygan, R. T.

    2015-12-07

    During the Frio-I Brine Pilot CO2 injection experiment in 2004, distinct geochemical changes in response to the injection of 1600 tons of CO2 were recorded in samples collected from the monitoring well. Previous geochemical modeling studies have considered dissolution of calcite and iron oxyhydroxides, or release of adsorbed iron, as the most likely sources of the increased ion concentrations. We explore in this modeling study possible alternative sources of the increasing calcium and iron, based on the data from the detailed petrographic characterization of the Upper Frio Formation “C”. Particularly, we evaluate whether dissolution of pyrite and oligoclase (anorthitemore » component) can account for the observed geochemical changes. Due to kinetic limitations, dissolution of pyrite and anorthite cannot account for the increased iron and calcium concentrations on the time scale of the field test (10 days). However, dissolution of these minerals is contributing to carbonate and clay mineral precipitation on the longer time scales (1000 years). The one-dimensional reactive transport model predicts carbonate minerals, dolomite and ankerite, as well as clay minerals kaolinite, nontronite and montmorillonite, will precipitate in the Frio Formation “C” sandstone as the system progresses towards chemical equilibrium during a 1000-year period. Cumulative uncertainties associated with using different thermodynamic databases, activity correction models (Pitzer vs. B-dot), and extrapolating to reservoir temperature, are manifested in the difference in the predicted mineral phases. Furthermore, these models are consistent with regards to the total volume of mineral precipitation and porosity values which are predicted to within 0.002%.« less