National Library of Energy BETA

Sample records for millivolt napl non-aqueous

  1. Non-Aqueous Phase Liquid Calculator

    Energy Science and Technology Software Center (OSTI)

    2004-02-19

    Non-Aqueous Phase Liquid or "NPAL" is a term that most environmental professionals are familiar with because NAPL has been recognized in the literature as a significant source of groundwater contamination. There are two types of NAPL: DNAPL and LNAPL. DNAPL is a ‘dense’ non-aqueous phase liquid. In this context, dense means having a density greater than water (1.0 kg/L). Trichloroethylene (TCE) and tetrachioroethylene (PCE) are examples of DNAPL compounds. A compound that is heaver thanmore » water means this type of NAPL will sink in an aquifer. Conversely, LNAPL is a ‘light’ non-aqueous phase liquid with a density less than water, and will float on top of the aquifer. Examples of LNAPL’s are benzene and toluene. LNAPL or DNAPL often manifest as a complex, multi-component mixture of organic compounds that can occur in environmental media. Complex multi-component mixtures distributed in soil pore-air, pore-water, soil particles and in free phase complicate residual saturation of single and multi component NAPL compounds in soil samples. The model output also includes estimates of the NAPL mass and volume and other physical and chemical properties that may be useful for characterization, modeling, and remedial system design and operation. The discovery of NAPL in the aquifer usually leads to a focused characterization for possible sources of NAPL in the vadose zone using a variety of innovative technologies and characterization methods. Often, the analytical data will indicated the presence of NAPL, yet, the NAPL will go unrecognized. Failure to recognize the NAPL can be attributed to the complicated processes of inter-media transfer or a general lack of knowledge about the physical characteristics of complex organic mixtures in environmental samples.« less

  2. Microsoft Word - DOE_RM_DM-#350832-v1-NAPL_Quarterly_April-June...

    Office of Legacy Management (LM)

    ... completed the final conceptual design for Area B NAPL remediation in early ... of Non-Aqueous Phase Liquids at the Northeast Site (Area B Conceptual Design) (DOE 2004). ...

  3. Microsoft Word - DOE_RM_DM-#345139-v1-NAPL_Quarterly_Oct-Dec...

    Office of Legacy Management (LM)

    ... completed the final conceptual design for Area B NAPL remediation in early ... of Non-Aqueous Phase Liquids at the Northeast Site (Area B Conceptual Design) (DOE 2004). ...

  4. Microsoft Word - DOE_RM_DM-#100069-v1-NAPL_Quarterly_Oct-Dec...

    Office of Legacy Management (LM)

    ... completed the final conceptual design for Area B NAPL remediation in early ... of Non-Aqueous Phase Liquids at the Northeast Site (Area B Conceptual Design) (DOE 2004). ...

  5. Non-aqueous liquid compositions comprising ion exchange polymers...

    Office of Scientific and Technical Information (OSTI)

    Data Explorer Search Results Non-aqueous liquid compositions comprising ion exchange polymers Title: Non-aqueous liquid compositions comprising ion exchange polymers Compositions, ...

  6. Inorganic rechargeable non-aqueous cell

    DOE Patents [OSTI]

    Bowden, William L. (Nashua, NH); Dey, Arabinda N. (Needham, MA)

    1985-05-07

    A totally inorganic non-aqueous rechargeable cell having an alkali or alkaline earth metal anode such as of lithium, a sulfur dioxide containing electrolyte and a discharging metal halide cathode, such as of CuCl.sub.2, CuBr.sub.2 and the like with said metal halide being substantially totally insoluble in SO.sub.2 and admixed with a conductive carbon material.

  7. NON-AQUEOUS DISSOLUTION OF MASSIVE PLUTONIUM

    DOE Patents [OSTI]

    Reavis, J.G.; Leary, J.A.; Walsh, K.A.

    1959-05-12

    A method is presented for obtaining non-aqueous solutions or plutonium from massive forms of the metal. In the present invention massive plutonium is added to a salt melt consisting of 10 to 40 weight per cent of sodium chloride and the balance zinc chloride. The plutonium reacts at about 800 deg C with the zinc chloride to form a salt bath of plutonium trichloride, sodium chloride, and metallic zinc. The zinc is separated from the salt melt by forcing the molten mixture through a Pyrex filter.

  8. Non-aqueous electrolyte for lithium-ion battery

    SciTech Connect (OSTI)

    Zhang, Lu; Zhang, Zhengcheng; Amine, Khalil

    2015-12-22

    An electrolyte including an alkali metal salt; a polar aprotic solvent; and a triazinane trione; wherein the electrolyte is substantially non-aqueous.

  9. Non-aqueous electrolytes for lithium-air batteries

    DOE Patents [OSTI]

    Amine, Khalil; Chen, Zonghai; Zhang, Zhengcheng

    2016-06-07

    A lithium-air cell includes a negative electrode; an air positive electrode; and a non-aqueous electrolyte which includes an anion receptor that may be represented by one or more of the formulas. ##STR00001##

  10. Northeast Site Non-Aqueous Phase Liquids Interim Measures Progress...

    Office of Legacy Management (LM)

    Northeast Site Non-Aqueous Phase Liquids Interim Measures Progress Report April 2003 Grand Junction Office U.S. Department of Energy Work Performed Under DOE Contract No. for the ...

  11. Naples, Maine: Energy Resources | Open Energy Information

    Open Energy Info (EERE)

    Naples, Maine: Energy Resources Jump to: navigation, search Equivalent URI DBpedia Coordinates 43.971739, -70.6092258 Show Map Loading map... "minzoom":false,"mappingservice":...

  12. Anion receptor compounds for non-aqueous electrolytes

    DOE Patents [OSTI]

    Lee, Hung Sui; Yang, Xiao-Oing; McBreen, James

    2000-09-19

    A new family of aza-ether based compounds including linear, multi-branched and aza-crown ethers is provided. When added to non-aqueous battery electrolytes, the new family of aza-ether based compounds acts as neutral receptors to complex the anion moiety of the electrolyte salt thereby increasing the conductivity and the transference number of LI.sup.+ ion in alkali metal batteries.

  13. Phenyl boron-based compounds as anion receptors for non-aqueous battery electrolytes

    DOE Patents [OSTI]

    Lee, Hung Sui; Yang, Xiao-Qing; McBreen, James; Sun, Xuehui

    2002-01-01

    Novel fluorinated boronate-based compounds which act as anion receptors in non-aqueous battery electrolytes are provided. When added to non-aqueous battery electrolytes, the fluorinated boronate-based compounds of the invention enhance ionic conductivity and cation transference number of non-aqueous electrolytes. The fluorinated boronate-based anion receptors include different fluorinated alkyl and aryl groups.

  14. Non-aqueous electrolytes for lithium ion batteries

    DOE Patents [OSTI]

    Chen, Zonghai; Amine, Khalil

    2015-11-12

    The present invention is generally related to electrolytes containing anion receptor additives to enhance the power capability of lithium-ion batteries. The anion receptor of the present invention is a Lewis acid that can help to dissolve LiF in the passivation films of lithium-ion batteries. Accordingly, one aspect the invention provides electrolytes comprising a lithium salt; a polar aprotic solvent; and an anion receptor additive; and wherein the electrolyte solution is substantially non-aqueous. Further there are provided electrochemical devices employing the electrolyte and methods of making the electrolyte.

  15. Non-aqueous electrolyte for lithium-ion battery

    DOE Patents [OSTI]

    Amine, Khalil; Zhang, Lu; Zhang, Zhengcheng

    2016-01-26

    A substantially non-aqueous electrolyte solution includes an alkali metal salt, a polar aprotic solvent, and an organophosphorus compound of Formula IA, IB, or IC: ##STR00001## where R.sup.1, R.sup.2, R.sup.3 and R.sup.4 are each independently hydrogen, halogen, alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heterocyclyl, heteroaryl, alkoxy, alkenoxy, alkynoxy, cycloalkoxy, aryloxy, heterocyclyloxy, heteroaryloxy, siloxyl, silyl, or organophosphatyl; R.sup.5 and R.sup.6 are each independently alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heterocyclyl, or heteroaryl; R.sup.7 is ##STR00002## and R.sup.8, R.sup.9 and R.sup.10 are each independently alkyl, cycloalkyl, aryl, heterocyclyl, or heteroaryl; provided that if the organophosphorus compound is of Formula IB, then at least one of R.sup.5, and R.sup.6 are other than hydrogen, alkyl, or alkenyl; and if the organophosphorus compound is of Formula IC, then the electrolyte solution does not include 4-methylene-1,3-dioxolan-2-one or 4,5-dimethylene-1,3-dioxolan-2-one.

  16. Microsoft Word - DOE_RM_DM-#99768-v1-NAPL_Quarterly_Report_for...

    Office of Legacy Management (LM)

    ... remediation process, an overview of construction and operation activities for NAPL Area ... of planning activities for the construction of a similar treatment system at NAPL ...

  17. Microsoft Word - N0071600-NAPL-Oct to Dec.doc

    Office of Legacy Management (LM)

    ... remediation process, an overview of construction and operation activities for NAPL Area ... planning activities for the construction of a similar treatment system at NAPL ...

  18. Microsoft Word - N0074600-NAPL-Jan to March.doc

    Office of Legacy Management (LM)

    remediation process, an overview of construction and operation activities for NAPL Area ... of planning activities for the construction of a similar treatment system at NAPL ...

  19. In Situ Thermal NAPL Remediation at the Northeast Site Pinellas Environmental Restoration Project

    SciTech Connect (OSTI)

    Juhlin, R.; Butherus, M.

    2006-07-01

    The U.S. Department of Energy (DOE) is conducting thermal remediation to remove non-aqueous phase liquids (NAPLs) from the subsurface at the Northeast Site that is part of the Pinellas Environmental Restoration Project. The Northeast Site is located on the Young - Rainey Science, Technology, and Research (STAR) Center in Largo, Florida. The STAR Center was formerly a DOE facility. The NAPL remediation was performed at Area A and is currently being performed at Area B at the Northeast Site. The remediation at Area A was completed in 2003 and covered an area of 900 m{sup 2} (10,000 ft{sup 2}) and a depth of remediation that extended to 10.7 m (35 ft) below ground surface. Cleanup levels achieved were at or below maximum contaminant levels in almost all locations. The remediation project at Area B is ongoing and covers an area of 3,240 m{sup 2} (36,000 ft{sup 2}), a volume of 41,300 m (54,000 yd 3), and a depth of remediation to 12 m (40 ft) below ground surface. In addition, a portion of the subsurface under an occupied building in Area B is included in the remediation. The cleanup levels achieved from this remediation will be available in the Area B Final Report that will be posted on the DOE Office of Legacy Management web site (www.lm.doe.gov/land/sites/fl/ pinellas/pinellas.htm) in January 2007. Electrical resistive heating and steam were the chosen remediation methods at both areas. Lessons learned from the Area A remediation were incorporated into the Area B remediation and could benefit managers of similar remediation projects. (authors)

  20. Northeast Site Non-Aqueous Phase Liquids Interim Measures Progress Report April through June 2003

    Office of Legacy Management (LM)

    7-TAC GJO-PIN 13.5.1-1 U.S. Department of Energy Work Performed Under DOE Contract No. for the U.S. Department of Energy DE-AC13-02GJ79491 Approved for public release; distribution is unlimited. Pinellas Environmental Restoration Project Northeast Site Non-Aqueous Phase Liquids Interim Measures Progress Report April Through June 2003 July 2003 N0063400 GJO- 2003- 467- TAC GJO-PIN 13.5.1-1 Pinellas Environmental Restoration Project Northeast Site Non-Aqueous Phase Liquids Interim Measures

  1. Non-aqueous spray drying as a route to ultrafine ceramic powders

    SciTech Connect (OSTI)

    Armor, J.N. ); Fanelli, A.J.; Marsh, G.M. ); Zambri, P.M. )

    1988-09-01

    Spray drying imparts unique powder handling features to a wide variety of dried products and is usually carried out in a heated air stream while feeding an aqueous suspension of some solid material. The present work, however, describes non-aqueous spray drying as a means of preparing fine powders of metal oxides. In this case an alcohol solvent was used in place of water and the slurry sprayed under an inert atmosphere. Using the non-aqueous technique, the product consists of distinct but loosely aggregated primary particles. Such materials have potential for use as catalysts or catalyst supports.

  2. Method and device for removing a non-aqueous phase liquid from a groundwater system

    DOE Patents [OSTI]

    Looney, Brian B.; Rossabi, Joseph; Riha, Brian D.

    2002-01-01

    A device for removing a non-aqueous phase liquid from a groundwater system includes a generally cylindrical push-rod defining an internal recess therein. The push-rod includes first and second end portions and an external liquid collection surface. A liquid collection member is detachably connected to the push-rod at one of the first and second end portions thereof. The method of the present invention for removing a non-aqueous phase liquid from a contaminated groundwater system includes providing a lance including an external hydrophobic liquid collection surface, an internal recess, and a collection chamber at the bottom end thereof. The lance is extended into the groundwater system such that the top end thereof remains above the ground surface. The liquid is then allowed to collect on the liquid collection surface, and flow downwardly by gravity into the collection chamber to be pumped upwardly through the internal recess in the lance.

  3. High voltage rechargeable magnesium batteries having a non-aqueous electrolyte

    DOE Patents [OSTI]

    Doe, Robert Ellis; Lane, George Hamilton; Jilek, Robert E.; Hwang, Jaehee

    2016-03-22

    A rechargable magnesium battery having an non-aqueous electrolyte is provided. The properties of the electrolyte include high conductivity, high Coulombic efficiency, and an electrochemical window that can exceed 3.5 V vs. Mg/Mg.sup.+2. The use of the electrolyte promotes the electrochemical deposition and dissolution of Mg without the use of any Grignard reagents, other organometallic materials, tetraphenyl borate, or tetrachloroaluminate derived anions. Other Mg-containing electrolyte systems that are expected to be suitable for use in secondary batteries are also described.

  4. Project Overview: Successful Field-Scale In Situ Thermal NAPL Remediation |

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

    Department of Energy Project Overview: Successful Field-Scale In Situ Thermal NAPL Remediation Project Overview: Successful Field-Scale In Situ Thermal NAPL Remediation Paper presented at the Third International Conference on Oxidation and Reduction Technologies for Soil and Groundwater. October 2004, San Diego, California. Michael Butherus, David S. Ingle, Randall Juhlin, Joseph Daniel Project Overview: Successful Field-Scale In Situ Thermal NAPL Remediation (305.82 KB) More Documents &

  5. Alkyl-bis(imidazolium) salts: a new amphiphile platform that forms thermotropic and non-aqueous lyotropic bicontinuous cubic phases

    SciTech Connect (OSTI)

    Robertson, LA; Schenkel, MR; Wiesenauer, BR; Gin, DL

    2013-01-01

    New ionic amphiphiles with a hexyl-bridged bis(imidazolium) headgroup; Br-, BF4-, or Tf2N- anions; and a long n-alkyl tail can form thermotropic bicontinuous cubic liquid crystal phases in neat form and/or lyotropic bicontinuous cubic phases with several non-aqueous solvents or water.

  6. Highly Quantitative Electrochemical Characterization of Non-Aqueous Electrolytes & Solid Electrolyte Interphases

    SciTech Connect (OSTI)

    Sergiy V. Sazhin; Kevin L. Gering; Mason K. Harrup; Harry W. Rollins

    2012-10-01

    The methods to measure solid electrolyte interphase (SEI) electrochemical properties and SEI formation capability of non-aqueous electrolyte solutions are not adequately addressed in the literature. And yet, there is a strong demand in new electrolyte generations that promote stabilized SEIs and have an influence to resolve safety, calendar life and other limitations of Li-ion batteries. To fill this gap, in situ electrochemical approach with new descriptive criteria for highly quantitative characterization of SEI and electrolytes is proposed. These criteria are: SEI formation capacity, SEI corrosion rate, SEI maintenance rate, and SEI kinetic stability. These criteria are associated with battery parameters like irreversible capacity, self-discharge, shelf-life, power, etc. Therefore, they are especially useful for electrolyte development and standard fast screening, allowing a skillful approach to narrow down the search for the best electrolyte. The characterization protocol also allows retrieving information on interfacial resistance for SEI layers and the electrochemical window of electrolytes, the other important metrics of characterization. The method validation was done on electrolyte blends containing phosphazenes, developed at Idaho National Laboratory, as 1.2M LiPF6 [80 % EC-MEC (2:8) (v/v) + 20% Phosphazene variety] (v/v), which were targeted for safer electrolyte variations.

  7. Shale gas and non-aqueous fracturing fluids: Opportunities and challenges for supercritical CO?

    SciTech Connect (OSTI)

    Middleton, Richard S.; Carey, James William; Currier, Robert P.; Hyman, Jeffrey De'Haven; Kang, Qinjun; Karra, Satish; Jimnez-Martnez, Joaqun; Porter, Mark L.; Viswanathan, Hari S.

    2015-06-01

    Hydraulic fracturing of shale formations in the United States has led to a domestic energy boom. Currently, water is the only fracturing fluid regularly used in commercial shale oil and gas production. Industry and researchers are interested in non-aqueous working fluids due to their potential to increase production, reduce water requirements, and to minimize environmental impacts. Using a combination of new experimental and modeling data at multiple scales, we analyze the benefits and drawbacks of using CO? as a working fluid for shale gas production. We theorize and outline potential advantages of CO? including enhanced fracturing and fracture propagation, reduction of flow-blocking mechanisms, increased desorption of methane adsorbed in organic-rich parts of the shale, and a reduction or elimination of the deep re-injection of flow-back water that has been linked to induced seismicity and other environmental concerns. We also examine likely disadvantages including costs and safety issues associated with handling large volumes of supercritical CO?. The advantages could have a significant impact over time leading to substantially increased gas production. In addition, if CO? proves to be an effective fracturing fluid, then shale gas formations could become a major utilization option for carbon sequestration.

  8. Shale gas and non-aqueous fracturing fluids: Opportunities and challenges for supercritical CO₂

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

    Middleton, Richard S.; Carey, James William; Currier, Robert P.; Hyman, Jeffrey De'Haven; Kang, Qinjun; Karra, Satish; Jiménez-Martínez, Joaquín; Porter, Mark L.; Viswanathan, Hari S.

    2015-06-01

    Hydraulic fracturing of shale formations in the United States has led to a domestic energy boom. Currently, water is the only fracturing fluid regularly used in commercial shale oil and gas production. Industry and researchers are interested in non-aqueous working fluids due to their potential to increase production, reduce water requirements, and to minimize environmental impacts. Using a combination of new experimental and modeling data at multiple scales, we analyze the benefits and drawbacks of using CO₂ as a working fluid for shale gas production. We theorize and outline potential advantages of CO₂ including enhanced fracturing and fracture propagation, reductionmore » of flow-blocking mechanisms, increased desorption of methane adsorbed in organic-rich parts of the shale, and a reduction or elimination of the deep re-injection of flow-back water that has been linked to induced seismicity and other environmental concerns. We also examine likely disadvantages including costs and safety issues associated with handling large volumes of supercritical CO₂. The advantages could have a significant impact over time leading to substantially increased gas production. In addition, if CO₂ proves to be an effective fracturing fluid, then shale gas formations could become a major utilization option for carbon sequestration.« less

  9. Shale gas and non-aqueous fracturing fluids: Opportunities and challenges for supercritical CO₂

    SciTech Connect (OSTI)

    Middleton, Richard S.; Carey, James William; Currier, Robert P.; Hyman, Jeffrey De'Haven; Kang, Qinjun; Karra, Satish; Jiménez-Martínez, Joaquín; Porter, Mark L.; Viswanathan, Hari S.

    2015-06-01

    Hydraulic fracturing of shale formations in the United States has led to a domestic energy boom. Currently, water is the only fracturing fluid regularly used in commercial shale oil and gas production. Industry and researchers are interested in non-aqueous working fluids due to their potential to increase production, reduce water requirements, and to minimize environmental impacts. Using a combination of new experimental and modeling data at multiple scales, we analyze the benefits and drawbacks of using CO₂ as a working fluid for shale gas production. We theorize and outline potential advantages of CO₂ including enhanced fracturing and fracture propagation, reduction of flow-blocking mechanisms, increased desorption of methane adsorbed in organic-rich parts of the shale, and a reduction or elimination of the deep re-injection of flow-back water that has been linked to induced seismicity and other environmental concerns. We also examine likely disadvantages including costs and safety issues associated with handling large volumes of supercritical CO₂. The advantages could have a significant impact over time leading to substantially increased gas production. In addition, if CO₂ proves to be an effective fracturing fluid, then shale gas formations could become a major utilization option for carbon sequestration.

  10. Containment and recovery of a light non-aqueous phase liquid plume at a woodtreating facility

    SciTech Connect (OSTI)

    Crouse, D.; Powell, G.; Hawthorn, S.; Weinstock, S.

    1997-12-31

    A woodtreating site in Montana used a formulation (product) of 5 percent pentachlorophenol and 95 percent diesel fuel as a carrier liquid to pressure treat lumber. Through years of operations approximately 378,500 liters of this light non-aqueous phase liquid (LNAPL) product spilled onto the ground and soaked into the groundwater. A plume of this LNAPL product flowed in a northerly direction toward a stream located approximately 410 meters from the pressure treatment building. A 271-meter long high density polyethylene (HDPE) containment cutoff barrier wall was installed 15 meters from the stream to capture, contain, and prevent the product from migrating off site. This barrier was extended to a depth of 3.7 meters below ground surface and allowed the groundwater to flow beneath it. Ten product recovery wells, each with a dual-phase pumping system, were installed within the plume, and a groundwater model was completed to indicate how the plume would be contained by generating a cone of influence at each recovery well. The model indicated that the recovery wells and cutoff barrier wall would contain the plume and prevent further migration. To date, nearly 3{1/2} year`s later, approximately 106,000 liters of product have been recovered.

  11. Synthesis and NMR characterization of SAPO-35 from non-aqueous systems using hexamethyleneimine template

    SciTech Connect (OSTI)

    Venkatathri, N. . E-mail: venkat@cata.ncl.res.in

    2005-07-12

    SAPO-35 was synthesized using hexamethyleneimine template in non-aqueous systems. X-ray diffraction and scanning electron micrograph analysis shows the synthesized sample is pure and well crystalline. Presence of four stages (1.6%, 0.8%, 7.8% and 8.4%) of weight loss is observed by TG/DTA analysis. FT-IR analysis in the framework region shows the presence of tetrahedral T-O-T vibrations is similar to the other known aluminophosphate molecular sieves. FT-IR spectrum in the -OH region shows stretching vibrations at 3631, 3604 and 3580 cm{sup -1} can be assigned to OH groups in bigger cages near S6R, in bigger cages near D6R and those actually confined inside the D6R, respectively. The spectra for the as-synthesized sample show a single symmetrical {sup 27}Al MAS NMR line at {delta} = 36.26 indicating the presence of a single tetrahedral aluminium species. Where as {sup 29}Si and {sup 31}P MAS NMR shows the presence of two peaks in both at (-89.9 and -95.15 ppm) and (-34.01 and -40.45 ppm) due to the Si substitution of P present in two different locations in double 6 ring (D6R) and in single 6 ring (S6R). {sup 27}Al 3Q-MAS NMR shows two peaks for environmentally different tetrahedral aluminium atoms. This is the first time we are showing such a fact which is not observable using ordinary MAS NMR.

  12. Niagara Air Quality Survey Report, 1987: Occidental Chemical Corporation, Niagara Falls, New York, USA, non-aqueous phase liquid (NAPL) incineration test. Report no. ARB-166-87-AR/SP

    SciTech Connect (OSTI)

    Bell, R.W.; DeBrou, G.

    1988-01-01

    An ambient air quality survey was conducted in the Niagara Falls area of Ontario from October 8-12, 1987 to provide on-site real-time screening for selected polychlorinated biphenyl congeners and other chlorinated organics at times when the Occidental Chemical Corporation was conducting tests at its liquid hazardous waste incineration facility in Niagara Falls, N.Y. During the incineration tests, the winds were such that the gaseous emissions from the Occidental facility were carried into the U.S. Since the monitoring units were restricted to the Canadian side of the Niagara River, only upwind air quality parameters could be measured.

  13. Successful Field-Scale In Situ Thermal NAPL Remediation at the Young -

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

    Rainey STAR Center | Department of Energy Successful Field-Scale In Situ Thermal NAPL Remediation at the Young - Rainey STAR Center Successful Field-Scale In Situ Thermal NAPL Remediation at the Young - Rainey STAR Center Proceedings of the Fourth International Conference on Remediation of Chlorinated and Recalcitrant Compounds. May 2004, Monterey, California. Randall Juhlin, Michael Butherus, Joseph Daniel, David S. Ingle, Dr. Gorm Heron, Dr. Bruce McGee Successful Field-Scale In Situ

  14. Quantitative Chromatographic Determination of Dissolved Elemental Sulfur in the Non-aqueous Electrolyte for Lithium-Sulfur Batteries

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

    Zheng, Dong; Yang, Xiao-Qing; Zhang, Xuran; Li, Chao; McKinnon, Meaghan E.; Sadok, Rachel G.; Qu, Deyu; Yu, Xiqian; Lee, Hung-Sui; Qu, Deyang

    2014-12-02

    A fast and reliable analytical method is reported for the quantitative determination of dissolved elemental sulfur in non-aqueous electrolytes for Li-S batteries. By using high performance liquid chromatography with a UV detector, the solubility of S in 12 different pure solvents and in 22 different electrolytes was determined. It was found that the solubility of elemental sulfur is dependent on the Lewis basicity, the polarity of solvents and the salt concentration in the electrolytes. In addition, the S content in the electrolyte recovered from a discharged Li-S battery was successfully determined by the proposed HPLC/UV method. Thus, the feasibility ofmore » the method to the online analysis for a Li-S battery is demonstrated. Interestingly, the S was found super-saturated in the electrolyte recovered from a discharged Li-S cell.« less

  15. Quantitative Chromatographic Determination of Dissolved Elemental Sulfur in the Non-aqueous Electrolyte for Lithium-Sulfur Batteries

    SciTech Connect (OSTI)

    Zheng, Dong; Yang, Xiao-Qing; Zhang, Xuran; Li, Chao; McKinnon, Meaghan E.; Sadok, Rachel G.; Qu, Deyu; Yu, Xiqian; Lee, Hung-Sui; Qu, Deyang

    2014-12-02

    A fast and reliable analytical method is reported for the quantitative determination of dissolved elemental sulfur in non-aqueous electrolytes for Li-S batteries. By using high performance liquid chromatography with a UV detector, the solubility of S in 12 different pure solvents and in 22 different electrolytes was determined. It was found that the solubility of elemental sulfur is dependent on the Lewis basicity, the polarity of solvents and the salt concentration in the electrolytes. In addition, the S content in the electrolyte recovered from a discharged Li-S battery was successfully determined by the proposed HPLC/UV method. Thus, the feasibility of the method to the online analysis for a Li-S battery is demonstrated. Interestingly, the S was found super-saturated in the electrolyte recovered from a discharged Li-S cell.

  16. Shale gas and non-aqueous fracturing fluids: Opportunities and challenges for supercritical CO2

    SciTech Connect (OSTI)

    Middleton, Richard Stephen; Carey, James William; Currier, Robert Patrick; Hyman, Jeffrey De'Haven; Kang, Qinjun; Karra, Satish; Viswanathan, Hari S.; Porter, Mark L.; Martinez, Joaquin Jimenez

    2015-03-23

    In this study, hydraulic fracturing of shale formations in the United States has led to a domestic energy boom. Currently, water is the only fracturing fluid regularly used in commercial shale oil and gas production. Industry and researchers are interested in non-aqueous working fluids due to their potential to increase production, reduce water requirements, and to minimize environmental impacts. Using a combination of new experimental and modeling data at multiple scales, we analyze the benefits and drawbacks of using CO2 as a working fluid for shale gas production. We theorize and outline potential advantages of CO2 including enhanced fracturing and fracture propagation, reduction of flow-blocking mechanisms, increased desorption of methane adsorbed in organic-rich parts of the shale, and a reduction or elimination of the deep re-injection of flow-back water that has been linked to induced seismicity and other environmental concerns. We also examine likely disadvantages including costs and safety issues associated with handling large volumes of supercritical CO2. The advantages could have a significant impact over time leading to substantially increased gas production. In addition, if CO2 proves to be an effective fracturing fluid, then shale gas formations could become a major utilization option for carbon sequestration.

  17. Refinement of the Kansas City Plant site conceptual model with respect to dense non-aqueous phase liquids (DNAPL)

    SciTech Connect (OSTI)

    Korte, N.E.; Hall, S.C.; Baker, J.L.

    1995-10-01

    This document presents a refinement of the site conceptual model with respect to dense non-aqueous phase liquid (DNAPL) at the US Department of Energy Kansas City Plant (KCP). This refinement was prompted by a review of the literature and the results of a limited study that was conducted to evaluate whether pools of DNAPL were present in contaminated locations at the KCP. The field study relied on the micropurge method of sample collection. This method has been demonstrated as a successful approach for obtaining discrete samples within a limited aquifer zone. Samples were collected at five locations across 5-ft well screens located at the base of the alluvial aquifer at the KCP. The hypothesis was that if pools of DNAPL were present, the dissolved concentration would increase with depth. Four wells with highly contaminated groundwater were selected for the test. Three of the wells were located in areas where DNAPL was suspected, and one where no DNAPL was believed to be present. The results demonstrated no discernible pattern with depth for the four wells tested. A review of the data in light of the available technical literature suggests that the fine-grained nature of the aquifer materials precludes the formation of pools. Instead, DNAPL is trapped as discontinuous ganglia that are probably widespread throughout the aquifer. The discontinuous nature of the DNAPL distribution prevents the collection of groundwater samples with concentrations approaching saturation. Furthermore, the results indicate that attempts to remediate the aquifer with conventional approaches will not result in restoration to pristine conditions because the tortuous groundwater flow paths will inhibit the efficiency of fluid-flow-based treatments.

  18. Microsoft Word - DOE_RM_DM-#344133-v1-Final_NAPL_Quarterly_July-Sept_2005.Dƒ

    Office of Legacy Management (LM)

    1 2005 - -L U.S. Department of Energy Work Performed Under DOE Contract No. for the U.S. Department of Energy Office of Legacy Management. DE-AC01-02GJ79491 Approved for public release; distribution is unlimited. Office of Legacy Management Office of Legacy Management Office of Legacy Management Pinellas Environmental Restoration Project Northeast Site Non-Aqueous Phase Liquids Interim Measure Progress Report July Through September 2005 October 2005 DOE-LM/GJ1011-2005 Pinellas Environmental

  19. U.S. DEPARTMENT OF ENERGY * SAVANNAH RIVER SITE * AIKEN * SC

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

    NAPL Calculator: (Non-aqueous Phase Liquid) An environmental engineer at the Savannah River Site has developed a software application that will determine if non-aqueous phase liquid (NAPL) contaminants are present in soil, groundwater, or soil vapor samples. The software will determine both the quantity and composition of NAPL chemicals in the samples based on the results of sample analysis. The software also computes important environmental engineering measures such as the residual saturation,

  20. Non-aqueous electrolytes for electrochemical cells

    DOE Patents [OSTI]

    Dong, Jian; Zhang, Zhengcheng; Amine, Khalil

    2016-07-12

    A electrolyte for a lithium battery includes a silane/siloxane compound represented by SiR.sub.4-x-yR'.sub.xR''.sub.y, by Formula II, or Formula III: ##STR00001## where each R is individually an alkenyl, alkynyl, alk(poly)enyl, alk(poly)ynyl, aryl; each R' is represented by; ##STR00002## each R'' is represented by Formula I-B; ##STR00003## R.sup.1 is an organic spacer; R.sup.2 is a bond or an organic spacer; R.sup.3 is alkyl or aryl; k is 1-15; m is 1-15; n is 1 or 2; p is 1-3; x' is 1-2; and y' is 0-2.

  1. Non-aqueous electrolytes for electrochemical cells

    DOE Patents [OSTI]

    Zhang, Zhengcheng; Dong, Jian; Amine, Khalil

    2016-06-14

    An electrolyte electrochemical device includes an anodic material and an electrolyte, the electrolyte including an organosilicon solvent, a salt, and a hybrid additiving having a first and a second compound, the hybrid additive configured to form a solid electrolyte interphase film on the anodic material upon application of a potential to the electrochemical device.

  2. NAPL Calculator - Energy Innovation Portal

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

    Programs http://nnsa.energy.gov printed copies are uncontrolled SUPPLEMENTAL DIRECTIVE Approved: 2-25-16 DEFENSE PROGRAMS BUSINESS PROCESS SYSTEM (DPBPS) NATIONAL NUCLEAR SECURITY ADMINISTRATION Office of Defense Programs NNSA SD 452.3-1A THIS PAGE INTENTIONALLY LEFT BLANK NNSA SD 452.3-1A 1 2-25-16 DEFENSE PROGRAMS BUSINESS PROCESS SYSTEM 1. PURPOSE. This supplemental directive (SD) establishes the Defense Programs Business Process System (DPBPS) Portal as the mechanism for implementing DOE

  3. Non-aqueous liquid compositions comprising ion exchange polymers

    DOE Patents [OSTI]

    Kim, Yu Seung; Lee, Kwan-Soo; Rockward, Tommy Q. T.

    2013-03-12

    Compositions, and methods of making thereof, comprising from about 1% to about 5% of a perfluorinated sulfonic acid ionomer or a hydrocarbon-based ionomer; and from about 95% to about 99% of a solvent, said solvent consisting essentially of a polyol; wherein said composition is substantially free of water and wherein said ionomer is uniformly dispersed in said solvent.

  4. Non-aqueous liquid compositions comprising ion exchange polymers

    DOE Patents [OSTI]

    Kim, Yu Seung; Lee, Kwan-Soo; Rockward, Tommy Q. T.

    2011-07-19

    Compositions, and methods of making thereof, comprising from about 1% to about 5% of a perfluorinated sulfonic acid ionomer or a hydrocarbon-based ionomer; and from about 95% to about 99% of a solvent, said solvent consisting essentially of a polyol; wherein said composition is substantially free of water and wherein said ionomer is uniformly dispersed in said solvent.

  5. Non-aqueous electrolyte for lithium-ion battery

    DOE Patents [OSTI]

    Zhang, Lu; Zhang, Zhengcheng; Amine, Khalil

    2014-04-15

    The present technology relates to stabilizing additives and electrolytes containing the same for use in electrochemical devices such as lithium ion batteries and capacitors. The stabilizing additives include triazinane triones and bicyclic compounds comprising succinic anhydride, such as compounds of Formulas I and II described herein.

  6. Non-aqueous electrolyte for high voltage rechargeable magnesium batteries

    DOE Patents [OSTI]

    Doe, Robert Ellis; Lane, George Hamilton; Jilek, Robert E; Hwang, Jaehee

    2015-02-10

    An electrolyte for use in electrochemical cells is provided. The properties of the electrolyte include high conductivity, high Coulombic efficiency, and an electrochemical window that can exceed 3.5 V vs. Mg/Mg.sup.+2. The use of the electrolyte promotes the electrochemical deposition and dissolution of Mg without the use of any Grignard reagents, other organometallic materials, tetraphenyl borate, or tetrachloroaluminate derived anions. Other Mg-containing electrolyte systems that are expected to be suitable for use in secondary batteries are also described.

  7. Non-aqueous electrolytes for lithium ion batteries (Patent) ...

    Office of Scientific and Technical Information (OSTI)

    Further there are provided electrochemical devices employing the electrolyte and methods of making the electrolyte. Inventors: Chen, Zonghai ; Amine, Khalil Issue Date: 2015-11-12 ...

  8. Non-aqueous solution preparation of doped and undoped lixmnyoz

    DOE Patents [OSTI]

    Boyle, Timothy J.; Voigt, James A.

    1997-01-01

    A method for generation of phase-pure doped and undoped Li.sub.x Mn.sub.y O.sub.z precursors. The method of this invention uses organic solutions instead of aqueous solutions or nonsolution ball milling of dry powders to produce phase-pure precursors. These precursors can be used as cathodes for lithium-polymer electrolyte batteries. Dopants may be homogeneously incorporated to alter the characteristics of the powder.

  9. Northeast Site Non-Aqueous Phase Liquids Interim Measures Progress...

    Office of Legacy Management (LM)

    5 Figure 3. Energy Balance......7 Figure 7. Treatment System Process Flow Diagram ... sent from there to the LNAPL and DNAPL waste storage tanks. ...

  10. Intermetallic negative electrodes for non-aqueous lithium cells and batteries

    DOE Patents [OSTI]

    Thackeray, Michael M.; Vaughey, John T.; Johnson, Christopher S.; Fransson, Linda M.; Edstrom, Ester Kristina; Henriksen, Gary

    2004-05-04

    A method of operating an electrochemical cell is disclosed. The cell has an intermetallic negative electrode of Cu.sub.6-x M.sub.x Sn.sub.5, wherein x is .ltoreq.3 and M is one or more metals including Si and a positive electrode containing Li in which Li is shuttled between the positive electrode and the negative electrode during charge and discharge to form a lithiated intermetallic negative electrode during charge. The voltage of the electrochemical cell is controlled during the charge portion of the charge-discharge cycles so that the potential of the lithiated intermetallic negative electrode in the fully charged electrochemical cell is less than 0.2 V but greater than 0 V versus metallic lithium.

  11. Non-aqueous electrolyte for lithium-ion battery (Patent) | DOEPatents

    Office of Scientific and Technical Information (OSTI)

    and R.sup.4 are each independently hydrogen, halogen, alkyl, alkenyl, alkynyl, ... of R.sup.5, and R.sup.6 are other than hydrogen, alkyl, or alkenyl; and if the ...

  12. Non-aqueous electrolyte for lithium-ion battery (Patent) | DOEPatents

    Office of Scientific and Technical Information (OSTI)

    States) Sponsoring Org: USDOE Country of Publication: United States Language: English Subject: 36 MATERIALS SCIENCE; 37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY

  13. Microscopic Insights into the Electrochemical Behavior of Non-aqueous Electrolytes in Supercapacitors

    SciTech Connect (OSTI)

    Jiang, Deen; Wu, Jianzhong

    2013-01-01

    Electric double-layer capacitors (EDLC) are electrical devices that store energy by adsorption of ionic species at the inner surface of porous electrodes. Compared with aqueous electrolytes, ionic liquid and organic electrolytes have the advantage of larger potential windows, making them attractive for the next generation of EDLC with superior energy and power densities. The performance of both ionic liquid and organic electrolyte EDLC hinges on the judicious selection of the electrode pore size and the electrolyte composition that requires a comprehension of the charging behavior from a microscopic view. In this perspective, we discuss predictions from the classical density functional theory (CDFT) on the dependence of the capacitance on the pore size for ionic-liquid and organic-electrolyte EDLC. CDFT is applicable to electrodes with the pore size ranging from that below the ionic dimensionality to mesoscopic scales, thus unique for investigating the electrochemical behavior of the confined electrolytes for EDLC applications.

  14. Non-aqueous liquid compositions comprising ion exchange polymers reference to related application

    DOE Patents [OSTI]

    Kim; Yu Seung , Lee; Kwan-Soo , Rockward; Tommy Q. T.

    2012-08-07

    Compositions, and methods of making thereof, comprising from about 1% to about 5% of a perfluorinated sulfonic acid ionomer or a hydrocarbon-based ionomer; and from about 95% to about 99% of a solvent, said solvent consisting essentially of a polyol; wherein said composition is substantially free of water and wherein said ionomer is uniformly dispersed in said solvent.

  15. Non-aqueous electrolyte for lithium-ion battery (Patent) | DOEPatents

    Office of Scientific and Technical Information (OSTI)

    Inventors: Zhang, Lu ; Zhang, Zhengcheng ; Amine, Khalil Issue Date: 2014-04-15 OSTI Identifier: 1129197 Assignee: UChicago Argonne, LLC (Chicago, IL) ANL Patent Number(s): ...

  16. Revised Arrangements for the Management of Solid and Non-Aqueous Radioactive Waste - 12452

    SciTech Connect (OSTI)

    Fullbrook, Michael; Walker, Johann; Macnab, Alec

    2012-07-01

    In 2010, Atomic Weapons Establishment (AWE) identified a requirement to implement revised management arrangements for the generation, storage and disposal of radioactive waste. A thorough review of the current arrangements/processes was undertaken which included both legal compliance requirements and the identification of business improvement opportunities. On completion of this review a suitable project team was established and in 2011 an integrated Radioactive Waste Management process was implemented throughout the business. Initial results have shown measurable improvements within Radioactive Waste management compliance, operator understanding and increased business efficiency. Through the development and implementation of the revised working arrangements AWE has been able to continue to demonstrate both legal compliance to its regulators along with business efficiency and effectiveness improvements. Simple to follow process maps have improved employees understanding of Radioactive Waste management requirements, provided them with easily accessible information and ensured the business operates in a single coherent manner. The implementation of a modern electronic data management system has ensured all waste related information is easily retrievable and appropriately maintained. The additional functions that have been built into the system have reduced the potential for human error and increased the overall efficiency of the Waste Management department through the use of the automated report generation functionality. (authors)

  17. Liquid Catholyte Molecules for Non-aqueous Redox Flow Batteries - Joint

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

    Liquefied Natural Gas Liquefied Natural Gas Liquefied Natural Gas Natural gas plays a vital role in the U.S. energy supply and in achieving the nation's economic and environmental goals. One of several supply options involves increasing imports of liquefied natural gas (LNG) to ensure that American consumers have adequate supplies of natural gas for the future. Natural gas consumption in the United States is expected to increase slightly from about 24.3 trillion cubic feet (Tcf) in 2011 to 26.6

  18. A Pentafluorophenylboron Oxalate Additive in Non-aqueous Electrolytes 3 for Lithium Batteries

    SciTech Connect (OSTI)

    Yang, X.Q.; Li, L.F.; Lee, H.S.; Li, H.; Huang, X.J.

    2009-12-01

    A novel compound named pentafluorophenylboron oxalate (PFPBO) has been synthesized. PFPBO has a unique molecular structure containing a boron atom center with electron deficiency and an oxalate group. It is found that when PFPBO is used as additive, the solubility of lithium fluoride (LiF) or lithium oxide (Li{sub 2}O, Li{sub 2}O{sub 2}) in propylene carbonate (PC) and dimethyl carbonate (DMC) solvents can be increased dramatically. The new electrolytes show high ionic conductivity, high lithium ion transference number and good compatibility with LiMn{sub 2}O{sub 4} cathode and MCMB anode. PFPBO was synthesized with the designed structure to act as a bi-functional additive: boron-based anion receptor (BBAR) additive and stable solid electrolyte interphase (SEI) formation additive in PC-based electrolytes. The results show it does possess these two desired functionalities.

  19. Understanding the Initial Stages of Reversible Mg Deposition and Stripping in Inorganic Non-Aqueous Electrolytes

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

    Canepa, Pieremanuele; Gautam, Gopalakrishnan Sai; Malik, Rahul; Jayaraman, Saivenkataraman; Rong, Ziqin; Zavadil, Kevin R.; Persson, Kristin; Ceder, Gerbrand

    2015-04-08

    Multivalent (MV) battery architectures based on pairing a Mg metal anode with a high-voltage (~3 V) intercalation cathode offer a realistic design pathway toward significantly surpassing the energy storage performance of traditional Li-ion-based batteries, but there are currently only few electrolyte systems that support reversible Mg deposition. Using both static first-principles calculations and ab initio molecular dynamics, we perform a comprehensive adsorption study of several salt and solvent species at the interface of Mg metal with an electrolyte of Mg2+ and Cl–dissolved in liquid tetrahydrofuran (THF). Our findings not only provide a picture of the stable species at the interfacemore » but also explain how this system can support reversible Mg deposition, and as such, we provide insights in how to design other electrolytes for Mg plating and stripping. Furthermore, the active depositing species are identified to be (MgCl)+ monomers coordinated by THF, which exhibit preferential adsorption on Mg compared to possible passivating species (such as THF solvent or neutral MgCl2 complexes). We found that upon deposition, the energy to desolvate these adsorbed complexes and facilitate charge transfer is shown to be small (~61–46.2 kJ mol–1 to remove three THF from the strongest adsorbing complex), and the stable orientations of the adsorbed but desolvated (MgCl)+ complexes appear to be favorable for charge transfer. Finally, observations of Mg–Cl dissociation at the Mg surface at very low THF coordinations (0 and 1) suggest that deleterious Cl incorporation in the anode may occur upon plating. In the stripping process, this is beneficial by further facilitating the Mg removal reaction.« less

  20. Non-aqueous electrolyte for lithium-ion battery (Patent) | DOEPatents

    Office of Scientific and Technical Information (OSTI)

    Patent Number(s): 9,218,915 Application Number: 14196,840 Contract Number: W-31-109-ENG-38 Resource Relation: Patent File Date: 2014 Mar 04 Research Org: Chicago Operations ...

  1. Origin of electrochemical, structural and transport properties in non-aqueous zinc electrolytes

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

    Han, Sang -Don; Rajput, Nav Nidhi; Qu, Xiaohui; Pan, Baofei; He, Meinan; Ferrandon, Magali S.; Liao, Chen; Persson, Kristin A.; Burrell, Anthony K.

    2016-01-14

    Through coupled experimental analysis and computational techniques, we uncover the origin of anodic stability for a range of nonaqueous zinc electrolytes. By examination of electrochemical, structural, and transport properties of nonaqueous zinc electrolytes with varying concentrations, it is demonstrated that the acetonitrile Zn(TFSI)2, acetonitrile Zn(CF3SO3)2, and propylene carbonate Zn(TFSI)2 electrolytes can not only support highly reversible Zn deposition behavior on a Zn metal anode (≥99% of Coulombic efficiency), but also provide high anodic stability (up to ~3.8 V). The predicted anodic stability from DFT calculations is well in accordance with experimental results, and elucidates that the solvents play an importantmore » role in anodic stability of most electrolytes. Molecular dynamics (MD) simulations were used to understand the solvation structure (e.g., ion solvation and ionic association) and its effect on dynamics and transport properties (e.g., diffusion coefficient and ionic conductivity) of the electrolytes. Lastly, the combination of these techniques provides unprecedented insight into the origin of the electrochemical, structural, and transport properties in nonaqueous zinc electrolytes« less

  2. Investigation of the Rechargeability of Li-O2 Batteries in Non-aqueous Electrolyte

    SciTech Connect (OSTI)

    Xiao, Jie; Hu, Jian Z.; Wang, Deyu; Hu, Dehong; Xu, Wu; Graff, Gordon L.; Nie, Zimin; Liu, Jun; Zhang, Jiguang

    2011-07-01

    In order to understand the nature of the limited cycle life and poor energy efficiency associated with the secondary Li-O2 batteries the discharge products of primary Li-O2 cells at different depth of discharge (DOD) are systematically analyzed in this work. It is revealed that if discharged to 2.0 V a small amount of Li2O2 coexist with Li2CO3 and RO-(C=O)-OLi) in alkyl carbonate-based electrolyte. Further discharging the air electrodes to below 2.0 V the amount of Li2CO3 and LiRCO3 increases significantly due to the severe electrolyte decomposition. There is no Li2O detected in this alkyl carbonate electrolyte regardless of DOD. It is also found that the alkyl carbonate based electrolyte begins to decompose at 4.0 V during charging under the combined influences from the high surface area carbon, the nickel metal current collector and the oxygen atmosphere. Accordingly the impedance of the Li-O2 cell continues to increase after each discharge and recharge process indicating a repeated plating of insoluble lithium salts on the carbon surface. Therefore the whole carbon electrode becomes completely insulated only after a few cycles and loses the function of providing active tri-phase regions for the Li-oxygen batteries.

  3. Understanding the Initial Stages of Reversible Mg Deposition and Stripping in Inorganic Non-Aqueous Electrolytes

    SciTech Connect (OSTI)

    Canepa, Pieremanuele; Gautam, Gopalakrishnan Sai; Malik, Rahul; Jayaraman, Saivenkataraman; Rong, Ziqin; Zavadil, Kevin R.; Persson, Kristin; Ceder, Gerbrand

    2015-04-08

    Multivalent (MV) battery architectures based on pairing a Mg metal anode with a high-voltage (~3 V) intercalation cathode offer a realistic design pathway toward significantly surpassing the energy storage performance of traditional Li-ion-based batteries, but there are currently only few electrolyte systems that support reversible Mg deposition. Using both static first-principles calculations and ab initio molecular dynamics, we perform a comprehensive adsorption study of several salt and solvent species at the interface of Mg metal with an electrolyte of Mg2+ and Cldissolved in liquid tetrahydrofuran (THF). Our findings not only provide a picture of the stable species at the interface but also explain how this system can support reversible Mg deposition, and as such, we provide insights in how to design other electrolytes for Mg plating and stripping. Furthermore, the active depositing species are identified to be (MgCl)+ monomers coordinated by THF, which exhibit preferential adsorption on Mg compared to possible passivating species (such as THF solvent or neutral MgCl2 complexes). We found that upon deposition, the energy to desolvate these adsorbed complexes and facilitate charge transfer is shown to be small (~6146.2 kJ mol1 to remove three THF from the strongest adsorbing complex), and the stable orientations of the adsorbed but desolvated (MgCl)+ complexes appear to be favorable for charge transfer. Finally, observations of MgCl dissociation at the Mg surface at very low THF coordinations (0 and 1) suggest that deleterious Cl incorporation in the anode may occur upon plating. In the stripping process, this is beneficial by further facilitating the Mg removal reaction.

  4. Final Report Northeast Site Area B NAPL Remediation Project

    Office of Legacy Management (LM)

    ... In order to seal the "gap" between the edge of asphalt and top of the geomembrane, a 1-inch thick cement- slurry "plug" was placed on top of the membrane. 2.4.4 Abandonment After ...

  5. Northeast Site Area A NAPL Remediation Final Report.doc

    Office of Legacy Management (LM)

    by U.S. Department of Energy Grand Junction Office ... 2.3 Steam System......the generation, handling, storage and transportation of ...

  6. Microsoft Word - N0075800-NAPL April to June 04.doc

    Office of Legacy Management (LM)

    ... water pollution prevention plan was finalized by the subcontractor by the end of June. The application for the modification of the existing synthetic non-Title V Air Emissions ...

  7. Kinetic investigation of catalytic disproportionation of superoxide ions in the non-aqueous electrolyte used in Liair batteries

    SciTech Connect (OSTI)

    Wang, Qiang; Zheng, Dong; McKinnon, Meaghan E.; Yang, Xiao -Qing; Qu, Deyang

    2014-10-28

    Superoxide reacts with carbonate solvents in Liair batteries. Tris(pentafluorophenyl)borane is found to catalyze a more rapid superoxide (O2-) disproportionation reaction than the reaction between superoxide and propylene carbonate (PC). With this catalysis, the negative impact of the reaction between the electrolyte and O2-produced by the O2 reduction can be minimized. A simple kinetic study using ESR spectroscopy was reported to determine reaction orders and rate constants for the reaction between PC and superoxide, and the disproportionation of superoxide catalyzed by Tris(pentafluorophenyl)borane and Li ions. As a result, the reactions are found to be first order and the rate constants are 0.033 s-1 M-1, 0.020 s-1 M-1and 0.67 s-1M-1 for reactions with PC, Li ion and Tris(pentafluorophenyl)borane, respectively.

  8. Protein-style dynamical transition in a non-biological polymer and a non-aqueous solvent

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

    Mamontov, E.; Sharma, V. K.; Borreguero, J. M.; Tyagi, M.

    2016-03-15

    Using neutron scattering and molecular dynamics simulation, techniques most often associated with protein dynamical transition studies, we have investigated the microscopic dynamics of one of the most common polymers, polystyrene, which was exposed to toluene vapor, mimicking the process of protein hydration from water vapor. Polystyrene with adsorbed toluene is an example of a solvent-solute system, which, unlike biopolymers, is anhydrous and lacks hydrogen bonding. Nevertheless, it exhibits the essential traits of the dynamical transition in biomolecules, such as a specific dependence of the microscopic dynamics of both solvent and host on the temperature and the amount of solvent adsorbed.more » Ultimately, we conclude that the protein dynamical transition is a manifestation of a universal solvent-solute dynamical relationship, which is not specific to either biomolecules as solute, or aqueous media as solvent, or even a particular type of interactions between solvent and solute.« less

  9. Literature search for the non-aqueous separation of zinc from fuel rod cladding. [After dissolution in liquid metal

    SciTech Connect (OSTI)

    Sandvig, R. L.; Dyer, S. J.; Lambert, G. A.; Baldwin, C. E.

    1980-06-21

    This report reviews the literature of processes for the nonaqueous separation of zinc from dissolved fuel assembly cladding. The processes considered were distillation, pyrochemical processing, and electrorefining. The last two techniques were only qualitatively surveyed while the first, distillation, was surveyed in detail. A survey of available literature from 1908 through 1978 on the distillation of zinc was performed. The literature search indicated that a zinc recovery rate in excess of 95% is possible; however, technical problems exist because of the high temperatures required and the corrosive nature of liquid zinc. The report includes a bibliography of the surveyed literature and a computer simulation of vapor pressures in binary systems. 129 references.

  10. Compatibility of Lithium Salts with Solvent of the Non-Aqueous Electrolyte in LiO2 Batteries

    SciTech Connect (OSTI)

    Du, Peng; Lu, Jun; Lau, Kah Chun; Luo, Xiangyi; Bareno, Javier; Zhang, Xiaoyi; Ren, Yang; Zhang, Zhengcheng; Curtiss, Larry A.; Sun, Yang-Kook; Amine, Khalil

    2013-02-20

    The stability of lithium salts, especially in the presence of reduced oxygen species, O2 and H2O (even in a small amount), plays an important role in the cyclability and capacity of LiO2 cells. This combined experimental and computational study provides evidence that the stability of the electrolyte used in LiO2 cells strongly depends on the compatibility of lithium salts with solvent. In the case of the LiPF61NM3 electrolyte, the decomposition of LiPF6 occurs in the cell as evidenced by in situ XRD, FT-IR and XPS analysis, which triggers the decomposition of 1NM3 solvent due to formation of HF from the decomposition of LiPF6. These reactions lead to degradation of the electrolyte and cause poor cyclability of the cell. The same reactions are not observed when LiTFSI and LiCF3SO3 are used as the lithium salts in 1NM3 solvent, or LiPF6 is used in TEGDME solvent.

  11. Kinetic investigation of catalytic disproportionation of superoxide ions in the non-aqueous electrolyte used in Li-air batteries

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

    Wang, Qiang; Yang, Xiao -Qing; Zheng, Doug; McKinnon, Meaghan E.; Qu, Deyang

    2014-10-28

    Superoxide reacts with carbonate solvents in Liair batteries. Tris(pentafluorophenyl)borane is found to catalyze a more rapid superoxide (O2-) disproportionation reaction than the reaction between superoxide and propylene carbonate (PC). With this catalysis, the negative impact of the reaction between the electrolyte and O2-produced by the O2 reduction can be minimized. A simple kinetic study using ESR spectroscopy was reported to determine reaction orders and rate constants for the reaction between PC and superoxide, and the disproportionation of superoxide catalyzed by Tris(pentafluorophenyl)borane and Li ions. The reactions are found to be first order and the rate constants are 0.033 s-1 M-1,more0.020 s-1 M-1and 0.67 s-1M-1 for reactions with PC, Li ion and Tris(pentafluorophenyl)borane, respectively.less

  12. Synthesis and studies of boron based anion receptors and their use in non-aqueous electrolytes for lithium batteries

    SciTech Connect (OSTI)

    Sun, X.; Yang, X.Q.; Lee, H.S.; McBreen, J.; Choi, L.S.

    1998-12-31

    A new family of anion receptors based on boron compounds has been synthesized. These compounds can be used as anion receptors in lithium battery electrolytes and can greatly increase solubility and ionic conductivities of various lithium salts, such as LiF, LiCl, CF{sub 3}COOLi and C{sub 2}F{sub 5}COOLi, in DME solutions. Near Edge X-ray Absorption Fine Structure (NEXAFS) spectroscopy studies show that Cl{sup {minus}} anions of LiCl are complexed with these compounds in DME solutions. The electrochemical stability of lithium salts and one of the boron compounds in deferent solvents was studied. For the first time, LiF has been successfully used as conducting salt in a novel electrolyte with this boron compound as an additive in DME. A rechargeable Li/LiMn{sub 2}O{sub 4} cell using this electrolyte was successfully cycled 51 times. However, the capacity fades with cycling due to decomposition of the solvent. The cycling performance of the battery was greatly improved by replacing DME with PC-EC-DMC as the solvent.

  13. Kinetic investigation of catalytic disproportionation of superoxide ions in the non-aqueous electrolyte used in Li–air batteries

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

    Wang, Qiang; Zheng, Dong; McKinnon, Meaghan E.; Yang, Xiao -Qing; Qu, Deyang

    2014-10-28

    Superoxide reacts with carbonate solvents in Li–air batteries. Tris(pentafluorophenyl)borane is found to catalyze a more rapid superoxide (O2-) disproportionation reaction than the reaction between superoxide and propylene carbonate (PC). With this catalysis, the negative impact of the reaction between the electrolyte and O2-produced by the O2 reduction can be minimized. A simple kinetic study using ESR spectroscopy was reported to determine reaction orders and rate constants for the reaction between PC and superoxide, and the disproportionation of superoxide catalyzed by Tris(pentafluorophenyl)borane and Li ions. As a result, the reactions are found to be first order and the rate constants aremore » 0.033 s-1 M-1, 0.020 s-1 M-1and 0.67 s-1M-1 for reactions with PC, Li ion and Tris(pentafluorophenyl)borane, respectively.« less

  14. Kinetic investigation of catalytic disproportionation of superoxide ions in the non-aqueous electrolyte used in Li-air batteries

    SciTech Connect (OSTI)

    Wang, Qiang; Yang, Xiao -Qing; Zheng, Doug; McKinnon, Meaghan E.; Qu, Deyang

    2014-10-28

    Superoxide reacts with carbonate solvents in Liair batteries. Tris(pentafluorophenyl)borane is found to catalyze a more rapid superoxide (O2-) disproportionation reaction than the reaction between superoxide and propylene carbonate (PC). With this catalysis, the negative impact of the reaction between the electrolyte and O2-produced by the O2 reduction can be minimized. A simple kinetic study using ESR spectroscopy was reported to determine reaction orders and rate constants for the reaction between PC and superoxide, and the disproportionation of superoxide catalyzed by Tris(pentafluorophenyl)borane and Li ions. The reactions are found to be first order and the rate constants are 0.033 s-1 M-1, 0.020 s-1 M-1and 0.67 s-1M-1 for reactions with PC, Li ion and Tris(pentafluorophenyl)borane, respectively.

  15. HYDROGEL TRACER BEADS: THE DEVELOPMENT, MODIFICATION, AND TESTING OF AN INNOVATIVE TRACER FOR BETTER UNDERSTANDING LNAPL TRANSPORT IN KARST AQUIFERS

    SciTech Connect (OSTI)

    Amanda Laskoskie, Harry M. Edenborn, and Dorothy J. Vesper

    2012-01-01

    The goal of this specific research task is to develop proxy tracers that mimic contaminant movement to better understand and predict contaminant fate and transport in karst aquifers. Hydrogel tracer beads are transported as a separate phase than water and can used as a proxy tracer to mimic the transport of non-aqueous phase liquids (NAPL). They can be constructed with different densities, sizes & chemical attributes. This poster describes the creation and optimization of the beads and the field testing of buoyant beads, including sampling, tracer analysis, and quantitative analysis. The buoyant beads are transported ahead of the dissolved solutes, suggesting that light NAPL (LNAPL) transport in karst may occur faster than predicted from traditional tracing techniques. The hydrogel beads were successful in illustrating this enhanced transport.

  16. Acoustically enhanced remediation of contaminated soils and ground water. Volume 1

    SciTech Connect (OSTI)

    1995-10-01

    The Phase 1 laboratory bench-scale investigation results have shown that acoustically enhanced remediation (AER) technology can significantly accelerate the ground water remediation of non-aqueous phase liquids (NAPLs) in unconsolidated soils. The testing also determined some of the acoustic parameters which maximize fluid and contaminant extraction rates. A technology merit and trade analysis identified the conditions under which AER could be successfully deployed in the field, and an analysis of existing acoustical sources and varying methods for their deployment found that AER technology can be successfully deployed in-situ. Current estimates of deployability indicate that a NAPL plume 150 ft in diameter can be readily remediated. This program focused on unconsolidated soils because of the large number of remediation sites located in this type of hydrogeologic setting throughout the nation. It also focused on NAPLs and low permeability soil because of the inherent difficult in the remediation of NAPLs and the significant time and cost impact caused by contaminated low permeability soils. This overall program is recommended for Phase 2 which will address the technology scaling requirements for a field scale test.

  17. Dynamic underground stripping to remediate a deep hydrocarbon spill

    SciTech Connect (OSTI)

    Yow, J.L. Jr.; Aines, R.D.; Newmark, R.L.

    1995-09-01

    Dynamic Underground Stripping is a combination of in situ steam injection, electrical resistance heating, and fluid extraction for rapid removal and recovery of subsurface contaminants such as solvents or fuels. Underground imaging and other measurement techniques monitor the system in situ for process control. Field tests at a deep gasoline spill at Lawrence Livermore National Laboratory recovered over 26,500 liters (7000 gallons) of gasoline during several months of field operations. Preliminary analysis of system cost and performance indicate that Dynamic Underground Stripping compares favorably with conventional pump-and-treat methods and vacuum extraction schemes for removing non-aqueous phase liquids (NAPLs) such as gasoline from deep subsurface plumes.

  18. N0057000.doc

    Office of Legacy Management (LM)

    000 GJO- 2002-380- TAC GJO-PIN 13.5.1-1 Pinellas Environmental Restoration Project Northeast Site Non-Aqueous Phase Liquids Interim Measures Progress Report July through September 2002 October 2002 Prepared by U.S. Department of Energy Grand Junction Office Grand Junction, Colorado Work Performed Under DOE Contract Number DE-AC13-02GJ79491 Task Order Number ST03-107 Document Number N0057000 Contents DOE/Grand Junction Office Northeast Site NAPL Interim Measures Progress Report October 2002 Page

  19. Non-aqueous solution preparation of doped and undoped Li{sub x}Mn{sub y}O{sub z}

    DOE Patents [OSTI]

    Boyle, T.J.; Voigt, J.A.

    1997-05-20

    A method is described for generation of phase-pure doped and undoped Li{sub x}Mn{sub y}O{sub z} precursors. The method of this invention uses organic solutions instead of aqueous solutions or nonsolution ball milling of dry powders to produce phase-pure precursors. These precursors can be used as cathodes for lithium-polymer electrolyte batteries. Dopants may be homogeneously incorporated to alter the characteristics of the powder. 1 fig.

  20. CO2 Capture and Regeneration at Low Temperatures: Novel Non-Aqueous CO2 Solvents and Capture Process with Substantially Reduced Energy Penalties

    SciTech Connect (OSTI)

    2010-07-01

    IMPACCT Project: RTI is developing a solvent and process that could significantly reduce the temperature associated with regenerating solvent and CO2 captured from the exhaust gas of coal-fired power plants. Traditional CO2 removal processes using water-based solvents require significant amount of steam from power plants in order to regenerate the solvent so it can be reused after each reaction. RTI’s solvents can be better at absorbing CO2 than many water-based solvents, and are regenerated at lower temperatures using less steam. Thus, industrial heat that is normally too cool to re-use can be deployed for regeneration, rather than using high-value steam. This saves the power plant money, which results in increased cost savings for consumers.

  1. Microsoft Word - DOE_RM_DM-#102768-v1-NAPL_Quarterly_Report_Jan...

    Office of Legacy Management (LM)

    .........2 4.0 Problems......a description of planning and construction ... Wiring for all these systems will be installed. An emergency ...

  2. Microsoft Word - DOE_RM_DM-#341474-v1-NAPL_Quarterly_April_-...

    Office of Legacy Management (LM)

    .........2 4.0 Problems......a description of planning and construction ... pumps, steam generator, emergency generator, and various ...

  3. Superfund Record of Decision (EPA Region 2): Hooker-102nd Street Landfill, Niagara Falls, NY. (First remedial action), September 1990. Final report

    SciTech Connect (OSTI)

    Not Available

    1990-09-26

    The 22-acre Hooker-102nd Street site is a former industrial landfill in the city of Niagara Falls, Niagara County, New York. The site is adjacent to, and partially within the Niagara River's 100-year floodplain. These studies and the Remedial Investigation (RI) initiated in 1984, identified contamination in ground water, onsite and offsite soil, rivershore sediment, and within a storm sewer. Additionally, the presence of a leachate plume of non-aqueous phase liquids (NAPLs) was discovered emanating from the landfill area. The Record of Decision (ROD) is the final remedy which addresses all of the contaminated media. The primary contaminants of concern affecting the soil, sediment, and ground water are VOCs including benzene, TCE, and toluene; other organics including PCBs and phenols; and metals including arsenic.

  4. Biotic and Abiotic Transformation of a Volatile Organics Plume in a Semi-Arid Vadose Zone

    SciTech Connect (OSTI)

    Studer, J.E.; Singletary, M.A.; Miller, D.R.

    1999-04-08

    An evaluation of biotic and abiotic attenuation processes potentially important to chlorinated and non-chlorinated volatile organic compound (VOC) fate and transport in the 148 meter thick vadose zone beneath the Chemical Waste Landfill (CWL) was conducted. A unique feature of this evaluation is the comparison of two estimates of VOC mass present in the soil gas, pore-water, and solid phases (but not including mass as non-aqueous phase liquid [NAPL]) of the vadose zone in 1993. One estimate, 1,800 kg, was obtained from vadose zone transport modeling that incorporated molecular diffusion and volatilization to the atmosphere, but not biotic or chemical processes. The other estimate, 2,120 kg, was obtained from the sum of VOC mass physically removed during soil vapor extraction and an estimate of VOC mass remaining in the vadose zone in 1998, both adjusted to exclude NAPL mass. This comparison indicates that biogeochemical processes were at best slightly important to historical VOC plume development. Some evidence of aerobic degradation of non-chlorinated VOCs and abiotic transformation of 1,1,1-Trichloroethane was identified. Despite potentially amenable site conditions, no evidence was found of cometabolic and anaerobic transformation pathways. Relying principally on soil-gas analytical results, an upper-bound estimate of 21% mass reduction due to natural biogeochemical processes was developed. Although available information for the CWL indicates that natural attenuation processes other than volatilization to the atmosphere did not effective y enhance groundwater protection, these processes could be important in significantly reducing groundwater contamination and exposure risks at other sites. More laboratory and field research is required to improve our collective ability to characterize and exploit natural VOC attenuation processes, especially with respect to the combination of relatively thick and dry vadose zones and chlorinated VOCs.

  5. Mass transfer and biodegradation of PAH compounds from coal tar. Quarterly technical report, January--March 1993

    SciTech Connect (OSTI)

    Ramaswami, A.; Ghoshal, S.; Luthy, R.G.

    1994-09-01

    This study examines the role of physico-chemical mass transfer processes on the rate of biotransformation of polycyclic aromatic hydrocarbon (PAH) compounds released from non-aqueous phase liquid (NAPL) coal tar present at residual saturation within a microporous medium. A simplified coupled dissolution-degradation model is developed that describes the concurrent mass transfer and biokinetic processes occurring in the system. Model results indicate that a dimensionless Damkohler number can be utilized to distinguish between systems that are mass transfer limited, and those that are limited by biological phenomena. The Damkohler number is estimated from independent laboratory experiments that measure the rates of aqueous phase dissolution and biodegradation of naphthalene from coal tar. Experimental data for Stroudsburg coal tar imbibed within 236 {mu}m diameter silica particles yield Damkohler numbers smaller than unity, indicating, for the particular system under study, that the overall rate of biotransformation of naphthalene is not limited by the mass transfer of naphthalene from coal tar to the bulk aqueous phase. There is a need for investigation of mass transfer for larger particles and/or other PAH compounds, and study of microbial rate-limiting phenomena including toxicity, inhibition and competitive substrate utilization.

  6. Buffalo County, Wisconsin: Energy Resources | Open Energy Information

    Open Energy Info (EERE)

    Wisconsin Modena, Wisconsin Mondovi, Wisconsin Montana, Wisconsin Naples, Wisconsin Nelson, Wisconsin Waumandee, Wisconsin Retrieved from "http:en.openei.orgw...

  7. Case study installation of a HDPE curtain wall with sheetpile tie-in on both ends

    SciTech Connect (OSTI)

    Schindler, R.M.; Maltese, P.C.

    1997-12-31

    The plans for eliminating the off-site migration of non-aqueous phase liquid (NAPL) from a refinery into a nearby river included the installation of a High Density Polyethylene (HDPE) curtain wall and an underdrain system. A 640 m (2100 lineal feet) HDPE Curtain Wall was installed along the river boundary, tying into an existing sheet pile wall on both ends. The wall varied from approximately 4.5 m (15 feet) deep at the northern end to about 7 m (23 feet) deep at the southern end, running approximately 3 to 3.6 m (10 to 12 feet) inland of an existing wooden bulkhead. The curtain wall was successfully installed through a slurry supported trench. A 930 m (3050 lineal feet) interception/collection trench was installed parallel to the HDPE Curtain Wall, continuing on beyond the curtain wall on the southern end. The depth of the trench varied from approximately 3 to 4 m (10 to 13 feet) deep. A 20.32 cm (8 inch) diameter perforated HDPE header pipe was placed in the trench to convey groundwater and product to two sumps. The trench is 53.34 cm (21 inches) wide and contained aggregate to approximately 0.9 m (3 feet) below ground. This work was accomplished using the bio-polymer slurry drainage trench (BP Drain) technique. This paper briefly describes the construction methods utilized during this project, specifically HDPE curtain wall installation thru a bentonite slurry and tie-in to the existing sheet pile wall.

  8. Tmvoc-React

    Energy Science and Technology Software Center (OSTI)

    2008-02-12

    The TMVOC-REACT simulator was generated by replacing the fluid and heat flow part, TOUGH2, in TOUGHREACT with TMVOC. Both programs have been distributed to the public through the US Department of Energy's Energy Science and Technology Software Center. TMVOC is a program for three-phase non-isothermal flows of multi-component hydrocarbon mixtures in variably saturated heterogeneous media. TMVOC was initially designed for studying subsurface contamination by volatile organic compounds (VOCs), such as hydrocarbon fuels and industrial solvents.more » It can model the one-, two-, or three-dimensional migration of non-aqueous phase liquids (NAPLs) through the unsaturated and saturated zones, the formation of an oil lens on the water table, the dissolution and subsequent transport of VOCs in groundwater, as well as the vaporization and migration of VOCs in the interstitial air of the unsaturated zone. TOUGHREACT is a numerical simulation program for chemically reactive nonisothermal flows of multiphase fluids in porous and fractured media. A variety of subsurface thermo-physical-chemical processes can be considered under a wide range of conditions of pressure, temperature, water saturation, ionic strength, pH and Eh. Intractions between mineral assemblages and fluids can occur under local equilibrium or kinetic rates. The gas phase can be chemically active. Precipitation and dissolution reactions can change formation porosity and permeability. The program can be applied to many geologic systems and environmental problems, including geothermal systems, diagenetic and weathering processes, subsurface waste disposal, aid mine drainage remediation, and contaminant transport.« less

  9. Property Transfer Review

    Office of Environmental Management (EM)

    Department of Energy Project Overview: Successful Field-Scale In Situ Thermal NAPL Remediation Project Overview: Successful Field-Scale In Situ Thermal NAPL Remediation Paper presented at the Third International Conference on Oxidation and Reduction Technologies for Soil and Groundwater. October 2004, San Diego, California. Michael Butherus, David S. Ingle, Randall Juhlin, Joseph Daniel Project Overview: Successful Field-Scale In Situ Thermal NAPL Remediation (305.82 KB) More Documents &

  10. Cumberland County, Maine: Energy Resources | Open Energy Information

    Open Energy Info (EERE)

    Maine Freeport, Maine Frye Island, Maine Gorham, Maine Gray, Maine Harpswell, Maine Harrison, Maine Little Falls-South Windham, Maine Long Island, Maine Naples, Maine New...

  11. Scott County, Illinois: Energy Resources | Open Energy Information

    Open Energy Info (EERE)

    Zone Subtype A. Places in Scott County, Illinois Alsey, Illinois Bluffs, Illinois Exeter, Illinois Glasgow, Illinois Manchester, Illinois Naples, Illinois Winchester, Illinois...

  12. EIS-0409: Mitigation Action Plan | Department of Energy

    Broader source: Energy.gov (indexed) [DOE]

    Draft Environmental Impact Statement EIS-0409: Final Environmental Impact Statement Successful Field-Scale In Situ Thermal NAPL Remediation at the Young - Rainey STAR Center...

  13. Remediation

    SciTech Connect (OSTI)

    Oostrom, Mart; Falta, Ron W.; Mayer, Alex S.; Javandel, I.; Hassanizadeh, S. M.

    2005-12-06

    The three most frequently used remediation technologies are discussed: (1) NAPL removal, (2) Pump-and-Treat, (3) Soil Vapor Extraction.

  14. Ontario County, New York: Energy Resources | Open Energy Information

    Open Energy Info (EERE)

    New York Naples, New York Phelps, New York Richmond, New York Rushville, New York Seneca, New York Shortsville, New York South Bristol, New York Victor, New York West...

  15. Clark County, South Dakota: Energy Resources | Open Energy Information

    Open Energy Info (EERE)

    Climate Zone Number 6 Climate Zone Subtype A. Places in Clark County, South Dakota Bradley, South Dakota Clark, South Dakota Garden City, South Dakota Naples, South Dakota...

  16. Boron compounds as anion binding agents for nonaqueous battery electrolytes

    DOE Patents [OSTI]

    Lee, Hung Sui; Yang, Xia-Oing; McBreen, James; Xiang, Caili

    2000-02-08

    Novel fluorinated boron-based compounds which act as anion receptors in non-aqueous battery electrolytes are provided. When added to non-aqueous battery electrolytes, the fluorinated boron-based compounds of the invention enhance ionic conductivity and cation transference number of non-aqueous electrolytes. The fluorinated boron-based anion receptors include borane and borate compounds bearing different fluorinated alkyl and aryl groups.

  17. Materials for Use with Aqueous Redox Flow Batteries | Argonne National

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

    Laboratory Materials for Use with Aqueous Redox Flow Batteries The invention provides a non-aqueous redox flow battery comprising a negative electrode immersed in a non-aqueous liquid negative electrolyte, a positive electrode immersed in a non-aqueous liquid positive electrolyte, and a cation-permeable separator (e.g., a porous membrane, film, sheet, or panel) between the negative electrolyte from the positive electrolyte. During charging and discharging, the electrolytes are circulated

  18. ZnS/Zn(O,OH)S-based buffer layer deposition for solar cells

    DOE Patents [OSTI]

    Bhattacharya, Raghu N.

    2009-11-03

    The invention provides CBD ZnS/Zn(O,OH)S and spray deposited ZnS/Zn(O,OH)S buffer layers prepared from a solution of zinc salt, thiourea and ammonium hydroxide dissolved in a non-aqueous/aqueous solvent mixture or in 100% non-aqueous solvent. Non-aqueous solvents useful in the invention include methanol, isopropanol and triethyl-amine. One-step deposition procedures are described for CIS, CIGS and other solar cell devices.

  19. Long life lithium batteries with stabilized electrodes (Patent...

    Office of Scientific and Technical Information (OSTI)

    The present invention relates to non-aqueous electrolytes having electrode stabilizing ... an alkali metal salt, a polar aprotic solvent, and an electrode stabilizing additive. ...

  20. Presentations | JCESR

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

    a Viable Lithium-Sulfur Transportation Battery Kevin Zavadil, JCESR Thrust PI, Chemical Transformation Pathways to Non-aqueous Redox Flow (NRF) Batteries for Grid Storage Fikile ...

  1. 2,5-Dimethoxy-1,4-Benzoquinone (DMBQ) as Organic Cathode for...

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

    Cathode for Rechargeable Magnesium-Ion Batteries Image for Organic Cathode Scientific ... non-aqueous rechargeable magnesium-ion batteries Significance and Impact Mg-DMBQ ...

  2. The mechanisms of oxygen reduction and evolution reactions in...

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

    and evolution reactions in nonaqueous lithium-oxygen batteries A mechanistic understanding of the oxygen reductionevolution reaction in non-aqueous lithium-oxygen batteries. ...

  3. Apparatus and methods for hydrocarbon extraction

    DOE Patents [OSTI]

    Bohnert, George W.; Verhulst, Galen G.

    2016-04-26

    Systems and methods for hydrocarbon extraction from hydrocarbon-containing material. Such systems and methods relate to extracting hydrocarbon from hydrocarbon-containing material employing a non-aqueous extractant. Additionally, such systems and methods relate to recovering and reusing non-aqueous extractant employed for extracting hydrocarbon from hydrocarbon-containing material.

  4. Apparatus for hydrocarbon extraction

    DOE Patents [OSTI]

    Bohnert, George W.; Verhulst, Galen G.

    2013-03-19

    Systems and methods for hydrocarbon extraction from hydrocarbon-containing material. Such systems and methods relate to extracting hydrocarbon from hydrocarbon-containing material employing a non-aqueous extractant. Additionally, such systems and methods relate to recovering and reusing non-aqueous extractant employed for extracting hydrocarbon from hydrocarbon-containing material.

  5. Removing sulphur oxides from a fluid stream

    DOE Patents [OSTI]

    Katz, Torsten; Riemann, Christian; Bartling, Karsten; Rigby, Sean Taylor; Coleman, Luke James Ivor; Lail, Marty Alan

    2014-04-08

    A process for removing sulphur oxides from a fluid stream, such as flue gas, comprising: providing a non-aqueous absorption liquid containing at least one hydrophobic amine, the liquid being incompletely miscible with water; treating the fluid stream in an absorption zone with the non-aqueous absorption liquid to transfer at least part of the sulphur oxides into the non-aqueous absorption liquid and to form a sulphur oxide-hydrophobic amine-complex; causing the non-aqueous absorption liquid to be in liquid-liquid contact with an aqueous liquid whereby at least part of the sulphur oxide-hydrophobic amine-complex is hydrolyzed to release the hydrophobic amine and sulphurous hydrolysis products, and at least part of the sulphurous hydrolysis products is transferred into the aqueous liquid; separating the aqueous liquid from the non-aqueous absorption liquid. The process mitigates absorbent degradation problems caused by sulphur dioxide and oxygen in flue gas.

  6. Saccharification of newspaper waste after ammonia fiber expansion...

    Office of Scientific and Technical Information (OSTI)

    ... Universitario Monte S. Angelo, Via Cintia, 4, 80126 Naples, Italy Full list of author information is available at the end of the article water by leachate, as well as air pollution ...

  7. CX-012256: Categorical Exclusion Determination

    Broader source: Energy.gov [DOE]

    Bench-Scale Development of a Non-Aqueous Solvent Carbon Dioxide Capture Process CX(s) Applied: B3.6 Date: 09/11/2014 Location(s): Norway Offices(s): National Energy Technology Laboratory

  8. CX-003172: Categorical Exclusion Determination

    Broader source: Energy.gov [DOE]

    RTI International - Novel Non-Aqueous Carbon Dioxide-Solvents and Capture ProcessCX(s) Applied: B3.6Date: 06/02/2010Location(s): North CarolinaOffice(s): Advanced Research Projects Agency - Energy

  9. Lithium metal oxide electrodes for lithium cells and batteries...

    Office of Scientific and Technical Information (OSTI)

    Title: Lithium metal oxide electrodes for lithium cells and batteries A lithium metal oxide positive electrode for a non-aqueous lithium cell is disclosed. The cell is prepared in ...

  10. Protein-Style Dynamical Transition in a non-Biological Polymer...

    Office of Scientific and Technical Information (OSTI)

    Protein-Style Dynamical Transition in a non-Biological Polymer and a non-Aqueous Solvent ... This content will become publicly available on January 1, 2017 Title: Protein-Style ...

  11. Four Scientific Approaches | JCESR

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

    and more inclusive than the specific battery technologies now being pursued by the ... Non-aqueous Redox Flow is based on reversibly - changing the charge state of ions held in ...

  12. Towards High-Performance Nonaqueous Redox Flow Electrolyte through Ionic Modification of Active Species

    SciTech Connect (OSTI)

    Wei, Xiaoliang; Cosimbescu, Lelia; Xu, Wu; Hu, Jian Z.; Vijayakumar, M.; Feng, Ju; Hu, Mary Y.; Deng, Xuchu; Xiao, Jie; Liu, Jun; Sprenkle, Vincent L.; Wang, Wei

    2015-01-01

    We will present a novel design lithium-organic non-aqueous redox flow battery based on a modified ferrocene catholyte. This RFB produced desired electrochemical performance exceeding most of the currently reported nonaqueous RFB systems.

  13. TEMPO-based Catholyte for High Energy Density Nonaqueous Redox Flow Batteries

    SciTech Connect (OSTI)

    Wei, Xiaoliang; Xu, Wu; Vijayakumar, M.; Cosimbescu, Lelia; Liu, Tianbiao L.; Sprenkle, Vincent L.; Wang, Wei

    2014-12-03

    We will present a novel design lithium-organic non-aqueous redox flow battery based on a TEMPO catholyte. This RFB produced desired electrochemical performance exceeding most of the currently reported nonaqueous RFB systems.

  14. Search for: All records | SciTech Connect

    Office of Scientific and Technical Information (OSTI)

    (1) fossil-fueled power plants(20) (1) geosciences (1) geosciences(58) (1) hydraulic fracturing (1) natural gas (1) natural gas(03) (1) non-aqueous fracturing fluids (1) oil shales...

  15. Complexes Containing Redox Non-Innocent Ligands for Symmetric,

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

    Multi-Electron Transfer Non-Aqueous Redox Flow Batteries - Joint Center for Energy Storage Research May 28, 2015, Research Highlights Complexes Containing Redox Non-Innocent Ligands for Symmetric, Multi-Electron Transfer Non-Aqueous Redox Flow Batteries (Top) Functionalized chromium bipyridine complexes (left), and solubility data for the charged and neutral species (right). (Bottom) Charge-discharge curves for the Cr(L3)3 complex: A) Full H-cell potential, B) Positive electrode potential,

  16. Transformer current sensor for superconducting magnetic coils

    DOE Patents [OSTI]

    Shen, S.S.; Wilson, C.T.

    1985-04-16

    The present invention is a current transformer for operating currents larger than 2kA (two kiloamps) that is capable of detecting a millivolt level resistive voltage in the presence of a large inductive voltage. Specifically, the present invention includes substantially cylindrical primary turns arranged to carry a primary current and substantially cylindrical secondary turns arranged coaxially with and only partially within the primary turns, the secondary turns including an active winding and a dummy winding, the active and dummy windings being coaxial, longitudinally separated and arranged to mutually cancel voltages excited by commonly experienced magnetic fields, the active winding but not the dummy winding being arranged within the primary turns.

  17. Thin film superconductors and process for making same

    DOE Patents [OSTI]

    Nigrey, P.J.

    1988-01-21

    A process for the preparation of oxide superconductors from high-viscosity non-aqueous solution is described. Solutions of lanthanide nitrates, alkaline earth nitrates and copper nitrates in a 1:2:3 stoichiometric ratio, when added to ethylene glycol containing citric acid solutions, have been used to prepare highly viscous non-aqueous solutions of metal mixed nitrates-citrates. Thin films of these compositions are produced when a layer of the viscous solution is formed on a substrate and subjected to thermal decomposition.

  18. DE-FE0013865 | netl.doe.gov

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

    Bench-Scale Development of a Non-Aqueous Solvent (NAS) CO2 Capture Process for Coal-Fired Power Plants Project No.: DE-FE0013865 Research Triangle Institute (RTI) is continuing the development process for a non-aqueous solvent (NAS)-based CO2 capture process that was originated at laboratory scale under an ARPA-E project. This project will conduct bench-scale testing to show the potential of the technology to reduce the parasitic energy penalty. Key technical and economic challenges and

  19. Lithium-titanium-oxide anodes for lithium batteries

    DOE Patents [OSTI]

    Vaughey, John T. (Elmhurst, IL); Thackeray, Michael M. (Naperville, IL); Kahaian, Arthur J. (Chicago, IL); Jansen, Andrew N. (Bolingbrook, IL); Chen, Chun-hua (Westmont, IL)

    2001-01-01

    A spinel-type structure with the general formula Li[Ti.sub.1.67 Li.sub.0.33-y M.sub.y ]O.sub.4, for 0non-aqueous electrochemical cell and in a non-aqueous battery comprising an plurality of cells, electrically connected, each cell comprising a negative electrode, an electrolyte and a positive electrode, the negative electrode consisting of the spinel-type structure disclosed.

  20. Negative electrodes for lithium cells and batteries

    DOE Patents [OSTI]

    Vaughey, John T.; Fransson, Linda M.; Thackeray, Michael M.

    2005-02-15

    A negative electrode is disclosed for a non-aqueous electrochemical cell. The electrode has an intermetallic compound as its basic structural unit with the formula M.sub.2 M' in which M and M' are selected from two or more metal elements including Si, and the M.sub.2 M' structure is a Cu.sub.2 Sb-type structure. Preferably M is Cu, Mn and/or Li, and M' is Sb. Also disclosed is a non-aqueous electrochemical cell having a negative electrode of the type described, an electrolyte and a positive electrode. A plurality of cells may be arranged to form a battery.

  1. Electrode compositions

    DOE Patents [OSTI]

    Block, J.; Fan, X.

    1998-10-27

    An electrode composition is described for use as an electrode in a non-aqueous battery system. The electrode composition contains an electrically active powder in a solid polymer and, as a dispersant, a C{sub 8}-C{sub 15} alkyl capped oligomer of a hexanoic acid that is electrochemically inert at 2.5--4.5 volts.

  2. High energy density battery based on complex hydrides

    DOE Patents [OSTI]

    Zidan, Ragaiy

    2016-04-26

    A battery and process of operating a battery system is provided using high hydrogen capacity complex hydrides in an organic non-aqueous solvent that allows the transport of hydride ions such as AlH.sub.4.sup.- and metal ions during respective discharging and charging steps.

  3. CX-010115: Categorical Exclusion Determination

    Broader source: Energy.gov [DOE]

    Non-Aqueous Titration of Next Generation Solvent in the Modular Caustic Side Solvent Extraction Unit CX(s) Applied: B3.6 Date: 03/28/2013 Location(s): South Carolina Offices(s): Savannah River Operations Office

  4. CX-010312: Categorical Exclusion Determination

    Broader source: Energy.gov [DOE]

    Dense Non-Aqueous Phase Liquid (DNAPL) Characterization at the M-Area Settling Basin Western Sector Treatment System (WSTS) CX(s) Applied: B3.1 Date: 04/26/2013 Location(s): South Carolina Offices(s): Savannah River Operations Office

  5. CX-013595: Categorical Exclusion Determination

    Broader source: Energy.gov [DOE]

    Non-Aqueous Titration of Next Generation Solvent in the Modular Caustic Side Solvent Extraction Unit (NGS-MCU) CX(s) Applied: B3.6Date: 03/19/2015Location(s): South CarolinaOffices(s): Savannah River Operations Office

  6. Electrode compositions

    DOE Patents [OSTI]

    Block, Jacob (Rockville, MD); Fan, Xiyun (Orange, TX)

    1998-01-01

    An electrode composition for use as an electrode in a non-aqueous battery system. The electrode composition contains an electrically active powder in a solid polymer and, as a dispersant, a C.sub.8 -C.sub.15 alkyl capped oligomer of a hexanoic acid that is electrochemically inert at 2.5-4.5 volts.

  7. Development of Chemical Model to Predict the Interactions between Supercritical CO2and Fluid, and Rocks in EGS Reservoirs

    Broader source: Energy.gov [DOE]

    This project will develop a chemical model, based on existing models and databases, that is capable of simulating chemical reactions between supercritical (SC) CO2 and Enhanced Geothermal System (EGS) reservoir rocks of various compositions in aqueous, non-aqueous and 2-phase environments.

  8. Fabrication of ionic liquid electrodeposited Cu--Sn--Zn--S--Se thin films and method of making

    DOE Patents [OSTI]

    Bhattacharya, Raghu Nath

    2016-01-12

    A semiconductor thin-film and method for producing a semiconductor thin-films comprising a metallic salt, an ionic compound in a non-aqueous solution mixed with a solvent and processing the stacked layer in chalcogen that results in a CZTS/CZTSS thin films that may be deposited on a substrate is disclosed.

  9. Electrogenerative oxidation of lower alcohols to useful products

    DOE Patents [OSTI]

    Meshbesher, Thomas M.

    1987-01-01

    In the disclosed electrogenerative process for converting alcohols such as ethanol to aldehydes such as acetaldehyde, the alcohol starting material is an aqueous solution containing more than the azeotropic amount of water. Good first-pass conversions (<40% and more typically <50%) are obtained at operating cell voltages in the range of about 80 to about 350 millivolts at ordinary temperatures and pressures by using very high flow rates of alcohol to the exposed anode surface (i.e. the "gas" side of an anode whose other surface is in contact with the electrolyte). High molar flow rates of vaporized aqueous alcohol also help to keep formation of undesired byproducts at a low level.

  10. Surface and Interfacial Properties of Nonaqueous-Phase Liquid Mixtures Released to the Subsurface at the Hanford Site

    SciTech Connect (OSTI)

    Nellis, Scott; Yoon, Hongkyu; Werth, Charlie; Oostrom, Martinus; Valocchi, Albert J.

    2009-05-01

    Surface and interfacial tensions that arise at the interface between different phases are key parameters affecting Nonaqueous Phase Liquid (NAPL) movement and redistribution in the vadose zone after spill events. In this study, the impact of major additive components on surface and interfacial tensions for organic mixtures and wastewater was investigated. Organic mixture and wastewater compositions are based upon carbon tetrachloride (CT) mixtures released at the Hanford site, where CT was discharged simultaneously with dibutyl butyl phosphonate (DBBP), tributyl phosphate (TBP), dibutyl phosphate (DBP), and a machining lard oil (LO). A considerable amount of wastewater consisting primarily of nitrates and metal salts was also discharged. The tension values measured in this study revealed that the addition of these additive components caused a significant lowering of the interfacial tension with water or wastewater and the surface tension of the wastewater phase in equilibrium with the organic mixtures, compared to pure CT, but had minimal effect on the surface tension of the NAPL itself. These results lead to large differences in spreading coefficients for several mixtures, where the additives caused both a higher (more spreading) initial spreading coefficient and a lower (less spreading) equilibrium spreading coefficient. This indicates that if these mixtures migrate into uncontaminated areas, they will tend to spread quickly, but form a higher residual NAPL saturation after equilibrium, as compared to pure CT. Over time, CT likely volatilizes more rapidly than other components in the originally disposed mixtures and the lard oil and phosphates would become more concentrated in the remaining NAPL, resulting in a lower interfacial tension for the mixture. Spreading coefficients are expected to increase and perhaps change the equilibrated organic mixtures from nonspreading to spreading in water-wetting porous media. These results show that the behavior of organic

  11. 1B-03.doc

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

    1B-03, in: A.R. Gavaskar and A.S.C. Chen (Eds.), Remediation of Chlorinated and Recalcitrant Compounds -2004. Proceedings of the Fourth International Conference on Remediation of Chlorinated and Recalcitrant Compounds (Monterey, CA; May 2004). ISBN 1-57477-145-0, published by Battelle Press, Columbus, OH, www.battelle.org/bookstore. NONAQUEOUS-PHASE LIQUID CHARACTERIZATION AND POST-REMEDIATION VERIFICATION SAMPLING ABSTRACT: Light and dense nonaqueous-phase liquids (NAPLs) were identified in the

  12. Proceedings of the international workshop on measurement and computation of turbulent nonpremixed flames

    SciTech Connect (OSTI)

    Barlow, R.S.

    1996-10-01

    This report documents the proceedings of the International Workshop on Measurement and Computation of Turbulent Nonpremixed Flames, held in Naples, Italy on July 26--27, 1996. Contents include materials that were distributed to participants at the beginning of the workshop, as well as a Summary of Workshop Accomplishments that was generated at the close to this Naples meeting. The Naples workshop involved sixty-one people from eleven countries. The primary objectives were: (1) to select a set of well-documented and relatively simple flames that would be appropriate for collaborative comparisons of model predictions; and (2) to specify common submodels to be used in these predictions, such that models for the coupling of turbulence and chemistry might be isolated and better understood. Studies involve hydrogen and natural gas fuels. These proceedings are also published on the Web and those interested in the ongoing process of data selection and model comparison should consult the workshop page for the most recent and complete information on these collaborative research efforts. The URL is: http://www/ca.sandia/gov/tdf/Workshop.html.

  13. Lead in human blood from children living in Campania, Italy

    SciTech Connect (OSTI)

    Amodio-Cocchieri, R.; Arnese, A.; Prospero, E.; Roncioni, A.

    1996-03-01

    Blood lead (PbB) levels were determined in children living Campania (in Naples and in a rural zone in the district of Caserta). Atmospheric lead (PbA) concentration in these considered areas was monitored for 1 yr (1993-1994). The children tested were questioned about common sources of lead, other than atmospheric relating to their living and dietary habits. The PbB levels in children living in Naples were at the 50th percentile, 18.8 {mu}g/dl in males and 13.7 {mu}g/dl in females; in children living in the rural area the median PbB levels were 8.9{mu}g/dl in males, and 9.9 {mu}g/dl in females. The annual mean values of atmospheres lead were 1.15 {plus_minus} 0.24 {mu}g/dl in Naples and 0.23 {plus_minus} 0.07 {mu}g/dl in the rural area. Significant and congruent mean differences between urban and rural sites were found in children`s blood and concurrent air lead. Considering the PbB level of 10 {mu}g/dl as the maximum level that is not associated any known adverse effect in children, the Neapolitan group can be considered at risk of chronic intoxication by lead. 18 refs., 3 figs., 4 tabs.

  14. CONTRIBUTING TO THE DISCUSSIONS ON THE FUNDAMENTAL ASPECTS AND COMPLEXITIES OF TALSPEAK CHEMISTRY

    SciTech Connect (OSTI)

    Peter R. Zalupski; Leigh R. Martin

    2011-10-01

    When liquid-liquid distribution of lanthanides was monitored at Talspeak-related conditions a characteristic drop in the extraction efficiency was observed at high lactate concentrations. The lactate dependency trend also appears to be directly affected by the increasing complexity of the non-aqueous environment. Some considerations of the non-ideal solution behavior in aqueous and organic environment are presented here in an attempt to explain the observed metal partitioning trends. While the mechanism of metal ion phase transfer appears to adhere to the conventional thermodynamic struggle between HDEHP and DTPA, the diminished metal distribution and suppressed slopes for the extractant dependencies suggest further build-up in the complexity of the non-aqueous environment in Talspeak systems.

  15. Method of remediation of contaminants in porous media through minimization of bouyancy effects

    DOE Patents [OSTI]

    Shook, G. Michael; Pope, Gary A.

    1999-01-01

    A method for controlling vertical migration of contaminants in an aquifer includes introduction of a solubilizing solution having a surfactant and an alcohol or other light co-solvent. The surfactant is selected to solubilize the contaminant. The alcohol or other solvent is selected to provide the microemulsion with a substantially neutral buoyancy with respect to groundwater. The neutral buoyancy of the microemulsion prevents the normal downward movement which is typical of the solubilized dense non-aqueous phase liquid in surfactant-enhanced aquifer remediation. Thus, the risk that any significant amount of the solubilized dense non-aqueous contaminants will migrate vertically can be controlled. The relative tendency for vertical migration may also be reduced by increasing the injection rate or injected fluid viscosity (by adding polymer), or by reducing the well spacing.

  16. Methods of making membrane electrode assemblies

    DOE Patents [OSTI]

    Kim, Yu Seung; Lee, Kwan -Soo; Rockward, Tommy Q. T.

    2015-07-28

    Method of making a membrane electrode assembly comprising: providing a membrane comprising a perfluorinated sulfonic acid; providing a first transfer substrate; applying to a surface of the first transfer substrate a first ink, said first ink comprising an ionomer and a catalyst; applying to the first ink a suitable non-aqueous swelling agent; forming an assembly comprising: the membrane; and the first transfer substrate, wherein the surface of the first transfer substrate comprising the first ink and the non-aqueous swelling agent is disposed upon one surface of the membrane; and heating the assembly at a temperature of 150.degree. C. or less and at a pressure of from about 250 kPa to about 3000 kPa or less for a time suitable to allow substantially complete transfer of the first ink and the second ink to the membrane; and cooling the assembly to room temperature and removing the first transfer substrate and the second transfer substrate.

  17. Ceramic porous material and method of making same

    DOE Patents [OSTI]

    Liu, Jun (Richland, WA); Kim, Anthony Y. (Kennewick, WA); Virden, Jud W. (Richland, WA)

    1997-01-01

    The invention is a mesoporous ceramic membrane having substantially uniform pore size. Additionally, the invention includes aqueous and non-aqueous processing routes to making the mesoporous ceramic membranes. According to one aspect of the present invention, inserting a substrate into a reaction chamber at pressure results in reaction products collecting on the substrate and forming a membrane thereon. According to another aspect of the present invention, a second aqueous solution that is sufficiently immiscible in the aqueous solution provides an interface between the two solutions whereon the mesoporous membrane is formed. According to a further aspect of the present invention, a porous substrate is placed at the interface between the two solutions permitting formation of a membrane on the surface or within the pores of the porous substrate. According to yet another aspect of the present invention, mesoporous ceramic materials are formed using a non-aqueous solvent and water-sensitive precursors.

  18. Ceramic porous material and method of making same

    DOE Patents [OSTI]

    Liu, J.; Kim, A.Y.; Virden, J.W.

    1997-07-08

    The invention is a mesoporous ceramic membrane having substantially uniform pore size. Additionally, the invention includes aqueous and non-aqueous processing routes to making the mesoporous ceramic membranes. According to one aspect of the present invention, inserting a substrate into a reaction chamber at pressure results in reaction products collecting on the substrate and forming a membrane thereon. According to another aspect of the present invention, a second aqueous solution that is sufficiently immiscible in the aqueous solution provides an interface between the two solutions whereon the mesoporous membrane is formed. According to a further aspect of the present invention, a porous substrate is placed at the interface between the two solutions permitting formation of a membrane on the surface or within the pores of the porous substrate. According to yet another aspect of the present invention, mesoporous ceramic materials are formed using a non-aqueous solvent and water-sensitive precursors. 21 figs.

  19. Hybrid energy storage systems utilizing redox active organic compounds

    DOE Patents [OSTI]

    Wang, Wei; Xu, Wu; Li, Liyu; Yang, Zhenguo

    2015-09-08

    Redox flow batteries (RFB) have attracted considerable interest due to their ability to store large amounts of power and energy. Non-aqueous energy storage systems that utilize at least some aspects of RFB systems are attractive because they can offer an expansion of the operating potential window, which can improve on the system energy and power densities. One example of such systems has a separator separating first and second electrodes. The first electrode includes a first current collector and volume containing a first active material. The second electrode includes a second current collector and volume containing a second active material. During operation, the first source provides a flow of first active material to the first volume. The first active material includes a redox active organic compound dissolved in a non-aqueous, liquid electrolyte and the second active material includes a redox active metal.

  20. Carbonation Mechanism of Reservoir Rock by Supercritical Carbon Dioxide |

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

    Department of Energy Carbonation Mechanism of Reservoir Rock by Supercritical Carbon Dioxide Carbonation Mechanism of Reservoir Rock by Supercritical Carbon Dioxide Project Objectives: Elucidate comprehensively the carbonation reaction mechanisms between supercritical carbon dioxide (scCO2) and reservoir rocks consisting of different mineralogical compositions in aqueous and non-aqueous environments at temperatures of up to 250ºC, and to develop chemical modeling of CO2-reservior rock

  1. Membrane reference electrode

    DOE Patents [OSTI]

    Redey, Laszlo; Bloom, Ira D.

    1989-01-01

    A reference electrode utilizes a small thin, flat membrane of a highly conductive glass placed on a small diameter insulator tube having a reference material inside in contact with an internal voltage lead. When the sensor is placed in a non-aqueous ionic electrolytic solution, the concentration difference across the glass membrane generates a low voltage signal in precise relationship to the concentration of the species to be measured with high spatial resolution.

  2. Accelerating Electrolyte Discovery for Energy Storage with High Throughput

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

    Screening - Joint Center for Energy Storage Research December 26, 2014, Research Highlights Accelerating Electrolyte Discovery for Energy Storage with High Throughput Screening A screening scheme has been developed to down-select molecule candidates based on successive property evaluations obtained from high-throughput computations. Here we show the down-select results for ~1400 candidates for non-aqueous redox flow battery application. Scientific Achievement We have developed a strategy to

  3. Technology available for license: Charging of liquid energy storage media

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

    through radiolysis (ANL-IN-14-036) | Argonne National Laboratory Technology available for license: Charging of liquid energy storage media through radiolysis (ANL-IN-14-036) January 23, 2015 Tweet EmailPrint This technology utilizes radiolysis to charge liquid energy storage media including nanoelectrofuels. Charged liquid can be used in flow batteries for transportation and stationary energy-storage applications. Radiolysis charging can be conducted on aqueous and non-aqueous battery

  4. Simplified one-pot synthesis of [.sup.18F]SFB for radiolabeling

    DOE Patents [OSTI]

    Olma, Sebastian; Shen, Clifton Kwang-Fu

    2013-07-16

    A non-aqueous single pot synthesis of [.sup.18F]SFB is set forth. The [.sup.18F]SFB produced with this method is then used, for example, to label a peptide or an engineered antibody fragment (diabody) targeting human epidermal growth factor receptor 2 (HER2) as representative examples of labeled compounds for use as an injectable composition to locate abnormal tissue, specifically tumors within an animal or human using a PET scan.

  5. Research Highlights - Joint Center for Energy Storage Research

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

    January 13, 2016, Research Highlights 2,5-Dimethoxy-1,4-Benzoquinone (DMBQ) as Organic Cathode for Rechargeable Magnesium-Ion Batteries 2,5-dimethoxyl-1,4-benzoquinone (DMBQ) was investigated as 2 V (vs Mg/Mg2+) organic cathode material for non-aqueous rechargeable magnesium-ion batteries Read More Multivalent Intercalation January 11, 2016, Research Highlights Simulations of Anodic Nanopore Growth Using the Smoothed Boundary and Level Set Methods A new numerical approach for simulating the

  6. Aza compounds as anion receptors

    DOE Patents [OSTI]

    Lee, H.S.; Yang, X.Q.; McBreen, J.

    1998-01-06

    A family of aza-ether based compounds including linear, multi-branched and aza-crown ethers is provided. When added to non-aqueous battery electrolytes, the family of aza-ether based compounds acts as neutral receptors to complex the anion moiety of the electrolyte salt thereby increasing the conductivity and the transference number of Li{sup +} ion in alkali metal batteries. 3 figs.

  7. Aza crown ether compounds as anion receptors

    DOE Patents [OSTI]

    Lee, H.S.; Yang, X.O.; McBreen, J.

    1998-08-04

    A family of aza-ether based compounds including linear, multi-branched and aza-crown ethers is provided. When added to non-aqueous battery electrolytes, the new family of aza-ether based compounds acts as neutral receptors to complex the anion moiety of the electrolyte salt thereby increasing the conductivity and the transference number of LI{sup +} ion in alkali metal batteries. 3 figs.

  8. Aza compounds as anion receptors

    DOE Patents [OSTI]

    Lee, Hung Sui; Yang, Xiao-Qing; McBreen, James

    1998-01-06

    A family of aza-ether based compounds including linear, multi-branched and aza-crown ethers is provided. When added to non-aqueous battery electrolytes, the family of aza-ether based compounds acts as neutral receptors to complex the anion moiety of the electrolyte salt thereby increasing the conductivity and the transference number of Li.sup.+ ion in alkali metal batteries.

  9. Aza crown ether compounds as anion receptors

    DOE Patents [OSTI]

    Lee, Hung Sui; Yang, Xiao-Oing; McBreen, James

    1998-08-04

    A family of aza-ether based compounds including linear, multi-branched and aza-crown ethers is provided. When added to non-aqueous battery electrolytes, the new family of aza-ether based compounds acts as neutral receptors to complex the anion moiety of the electrolyte salt thereby increasing the conductivity and the transference number of LI.sup.+ ion in alkali metal batteries.

  10. PROTACTINIUM EXTRACTION

    DOE Patents [OSTI]

    Horn, F.L.

    1962-07-24

    A method of producing and separating protactinium from taorium containing solids is described. The protactinium is formed by irradiating thorium containing solids, such as thorium dioxide and thorium tetrafluoride with neutrons. The protactinium is separated from the thorium solids by contacting the solids with a non-squeous solution of hydrogen fluoride and a complexing agent, NO/sub 2/. The protactinium complex formed is soluble in the non-aqueous solution, whereas the thorium solids remain insoluble in the solution. (AEC)

  11. Presentations - Joint Center for Energy Storage Research

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

    Presentations To view notes or play video, please download. JCESR Presentations at the 228th Electrochemical Society Meeting, Phoenix, AZ (10-11-15) The Joint Center for Energy Storage Research (JCESR): A New Paradigm for Energy Storage Research George Crabtree, JCESR Director Overcoming Key Challenges for a Viable Lithium-Sulfur Transportation Battery Kevin Zavadil, JCESR Thrust PI, Chemical Transformation Pathways to Non-aqueous Redox Flow (NRF) Batteries for Grid Storage Fikile Brushett,

  12. Long Life Lithium Batteries with Stabilized Electrodes | Argonne National

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

    Laboratory Long Life Lithium Batteries with Stabilized Electrodes Technology available for licensing: Non-aqueous electrolytes with stabilization additives for improved calendar and cycle life of batteries Additives enable excellent specific power and energy and extended calendar life Work across broad temperature range with minimal or no capacity loss IN-03-047 US 7968235B2 US 8551661B2 Availability: Technology available for license to organizations with commercial interest. Collaborative

  13. Simplified one-pot synthesis of [.sup.18F]SFB for radiolabeling

    DOE Patents [OSTI]

    Olma, Sebastian; Shen, Clifton Kwang-Fu

    2015-08-04

    A non-aqueous single pot synthesis of [.sup.18F]SFB is set forth. The [.sup.18F]SFB produced with this method is then used, for example, to label a peptide or an engineered antibody fragment (diabody) targeting human epidermal growth factor receptor 2 (HER2) as representative examples of labeled compounds for use as an injectable composition to locate abnormal tissue, specifically tumors within an animal or human using a PET scan.

  14. Membrane reference electrode

    DOE Patents [OSTI]

    Redey, L.; Bloom, I.D.

    1988-01-21

    A reference electrode utilizes a small thin, flat membrane of a highly conductive glass placed on a small diameter insulator tube having a reference material inside in contact with an internal voltage lead. When the sensor is placed in a non-aqueous ionic electrolytic solution, the concentration difference across the glass membrane generates a low voltage signal in precise relationship to the concentration of the species to be measured, with high spatial resolution. 2 figs.

  15. Microbial production of epoxides

    DOE Patents [OSTI]

    Clark, Thomas R.; Roberto, Francisco F.

    2003-06-10

    A method for microbial production of epoxides and other oxygenated products is disclosed. The method uses a biocatalyst of methanotrophic bacteria cultured in a biphasic medium containing a major amount of a non-aqueous polar solvent. Regeneration of reducing equivalents is carried out by using endogenous hydrogenase activity together with supplied hydrogen gas. This method is especially effective with gaseous substrates and cofactors that result in liquid products.

  16. solvent-battelle | netl.doe.gov

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

    CO2 Binding Organic Liquids Gas Capture with Polarity-Swing-Assisted Regeneration Project No.: DE-FE0007466 Battelle Pacific Northwest Division is developing a new CO2 capture technology for treating post-combustion emissions. The new process couples the unique attributes of non-aqueous, switchable organic solvents (CO2 binding organic liquids - CO2BOLs) with the newly discovered polarity-swing-assisted regeneration (PSAR) process. The process requires significantly lower temperatures and

  17. Frozen soil barriers for hazardous waste confinement

    SciTech Connect (OSTI)

    Dash, J.G.; Leger, R.; Fu, H.Y.

    1997-12-31

    Laboratory and full field measurements have demonstrated the effectiveness of artificial ground freezing for the containment of subsurface hazardous and radioactive wastes. Bench tests and a field demonstration have shown that cryogenic barriers are impenetrable to aqueous and non aqueous liquids. As a result of the successful tests the US Department of Energy has designated frozen ground barriers as one of its top ten remediation technologies.

  18. Chemical Transformation - Joint Center for Energy Storage Research

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

    July 28, 2014, Research Highlights Formation of Interfacial Layer and Long-Term Cyclability of Li-O2 Batteries Identified key factors that affect the long term cycle life of Li-O2 batteries under full discharge/charge conditions. Read More Chemical Transformation July 8, 2014, Research Highlights The mechanisms of oxygen reduction and evolution reactions in nonaqueous lithium-oxygen batteries Superoxide radical anions (O2*-) are intermediates formed in non-aqueous lithium-oxygen batteries, which

  19. Pentavalent Uranium Chemistry - Synthetic Pursuit Of A Rare Oxidation State

    SciTech Connect (OSTI)

    Graves, Christopher R; Kiplinger, Jaqueline L

    2009-01-01

    This feature article presents a comprehensive overview of pentavalent uranium systems in non-aqueous solution with a focus on the various synthetic avenues employed to access this unusual and very important oxidation state. Selected characterization data and theoretical aspects are also included. The purpose is to provide a perspective on this rapidly evolving field and identify new possibilities for future developments in pentavalent uranium chemistry.

  20. Kuwaiti oil sector shows more signs of recovery

    SciTech Connect (OSTI)

    Not Available

    1992-04-06

    This paper reports that Kuwait's oil sector continues to show signs of recovery from the Persian Gulf war. On Mar. 23 Kuwait Petroleum Co. (KPC) loaded the country's first shipment of liquefied petroleum gas for export since the Iraqi invasion in August 1990. In addition, the first shipment of Kuwaiti crude recovered from giant oil lakes formed by hundreds of wild wells sabotaged in the war was to arrive by tanker in Naples, Italy, late last month. The tanker is carrying 210,000 bbl of crude. However, the project to clean up the lakes and recover more oil, undertaken by Bechtel Corp. with Kuwait Oil Co. (KOC), has reached a stand still.

  1. SREL Reprint #3230

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

    0 Foraging Habitat Use by Breeding Wood Storks and the Core Foraging Area Concept A. Lawrence Bryan, Jr.1, Ken D. Meyer2, Bree A. Tomlinson3, Jason A. Lauritsen4, and William B. Brooks5 1Savannah River Ecology Laboratory, P.O. Drawer E, Aiken, SC 29802, USA 2Avian Research and Conservation Institute, Gainesville, FL, 32601, USA 3College of Charleston, Charleston, SC, 29424, USA 4National Audubon Society, Corkscrew Swamp Sanctuary, Naples, FL, 34120, USA 5U.S. Fish and Wildlife Service, North

  2. Appearance of thermochemical emf in some conducting materials

    SciTech Connect (OSTI)

    Petrov, Y.S.; Maslikhov, V.V.; Shcheglov, V.D.

    1983-05-01

    The appearance of an emf in conductors when they are heated is described by the Seebeck and Thompson effects. If some part of the surface of a conductor is covered by a pyrotechnical material and ignited, then while the pyrotechnical material is burning and after it has burned, an emf arises at the ends of the conductor. The direction of the emf depends on the location of maximum temperature of the heated section of the conductor. If the heating is terminated for some time and started up again, then the emf and current appear again, with no necessity for re-application of the pyrotechnical material. Conductors of Nichrome, Constantan and tungsten, as well as graphite rods were studied with small sections of the conductors covered with lead azide, black gunpowder, or match-head composition. The current ranged from -5 to 6 microamps, and the emf from -0.4 to 1 millivolt. The effects described can be used to convert thermal energy into electrical energy in sensors, etc.

  3. Development of thermoelectric fibers for miniature thermoelectric devices

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

    Ren, Fei; Menchhofer, Paul A.; Kiggans, Jr., James O.; Wang, Hsin

    2016-09-23

    Miniature thermoelectric (TE) devices may be used in a variety of applications such as power sources of small sensors, temperature regulation of precision electronics, etc. Reducing the size of TE elements may also enable design of novel devices with unique form factor and higher device efficiency. Current industrial practice of fabricating TE devices usually involves mechanical removal processes that not only lead to material loss but also limit the geometry of the TE elements. In this project, we explored a powder-processing method for the fabrication of TE fibers with large length-to-area ratio, which could be potentially used for miniature TEmore » devices. Powders were milled from Bi2Te3-based bulk materials and then mixed with a thermoplastic resin dissolved in an organic solvent. Through an extrusion process, flexible, continuous fibers with sub-millimeter diameters were formed. The polymer phase was then removed by sintering. Sintered fibers exhibited similar Seebeck coefficients to the bulk materials. Moreover, their electrical resistivity was much higher, which might be related to the residual porosity and grain boundary contamination. Prototype miniature uni-couples fabricated from these fibers showed a linear I-V behavior and could generate millivolt voltages and output power in the nano-watt range. Further development of these TE fibers requires improvement in their electrical conductivities, which needs a better understanding of the causes that lead to the low conductivity in the sintered fibers.« less

  4. Novel air electrode for metal-air battery with new carbon material and method of making same

    DOE Patents [OSTI]

    Ross, Jr., Philip N.

    1990-01-01

    A novel carbonaceous electrode support material is disclosed characterized by a corrosion rate of 0.03 wt. %/hour or less when measured a5 550 millivolts vs. a Hg/HgO electrode in a 30 wt. % KOH electrolyte a5 30.degree. C. The electrode support material comprises a preselected carbon black material which has been heat-treated by heating the material to a temperature of from about 2500.degree. to about 3000.degree. C. over a period of from about 1 to about 5 hours in an inert atmosphere and then maintaining the preselected carbon black material at this temperature for a period of at least about 1 hour, and preferably about 2 hours, in the inert atmosphere. A carbonaceous electrode suitable for use as an air electrode in a metal-air cell may be made from the electrode support material by shaping and forming it into a catalyst support and then impregnating it with a catalytically active material capable of catalyzing the reaction with oxygen at the air electrode of metal-air cell.

  5. Chemical overcharge protection of lithium and lithium-ion secondary batteries

    DOE Patents [OSTI]

    Abraham, Kuzhikalail M.; Rohan, James F.; Foo, Conrad C.; Pasquariello, David M.

    1999-01-01

    This invention features the use of redox reagents, dissolved in non-aqueous electrolytes, to provide overcharge protection for cells having lithium metal or lithium-ion negative electrodes (anodes). In particular, the invention features the use of a class of compounds consisting of thianthrene and its derivatives as redox shuttle reagents to provide overcharge protection. Specific examples of this invention are thianthrene and 2,7-diacetyl thianthrene. One example of a rechargeable battery in which 2,7-diacetyl thianthrene is used has carbon negative electrode (anode) and spinet LiMn.sub.2 O.sub.4 positive electrode (cathode).

  6. Chemical overcharge protection of lithium and lithium-ion secondary batteries

    DOE Patents [OSTI]

    Abraham, K.M.; Rohan, J.F.; Foo, C.C.; Pasquariello, D.M.

    1999-01-12

    This invention features the use of redox reagents, dissolved in non-aqueous electrolytes, to provide overcharge protection for cells having lithium metal or lithium-ion negative electrodes (anodes). In particular, the invention features the use of a class of compounds consisting of thianthrene and its derivatives as redox shuttle reagents to provide overcharge protection. Specific examples of this invention are thianthrene and 2,7-diacetyl thianthrene. One example of a rechargeable battery in which 2,7-diacetyl thianthrene is used has carbon negative electrode (anode) and spinet LiMn{sub 2}O{sub 4} positive electrode (cathode). 8 figs.

  7. Heteroatom incorporated coke for electrochemical cell electrode

    DOE Patents [OSTI]

    Lewis, Irwin Charles (Strongsville, OH); Greinke, Ronald Alfred (Medina, OH)

    1997-01-01

    This invention relates to an electrode for a coke/alkali metal electrochemical cell comprising: (a) calcined coke particles: (i) that contain at least 0.5 weight percent of nitrogen heteroatoms and at least 1.0 weight percent sulfur heteroatoms, and (ii) that have an average particle size from 2 microns to 40 microns with essentially no particles being greater than 50 microns. (b) a binder This invention also relates to a coke/alkali metal electrochemical cell comprising: (a) an electrode as described above, (b) a non-aqueous electrolytic solution comprising an organic aprotic solvent and an electrically conductive salt, and (c) a counterelectrode.

  8. Heteroatom incorporated coke for electrochemical cell electrode

    DOE Patents [OSTI]

    Lewis, I.C.; Greinke, R.A.

    1997-06-17

    This invention relates to an electrode for a coke/alkali metal electrochemical cell comprising: (a) calcined coke particles: (1) that contain at least 0.5 weight percent of nitrogen heteroatoms and at least 1.0 weight percent sulfur heteroatoms, and (2) that have an average particle size from 2 microns to 40 microns with essentially no particles being greater than 50 microns and (b) a binder. This invention also relates to a coke/alkali metal electrochemical cell comprising: (a) an electrode as described above, (b) a non-aqueous electrolytic solution comprising an organic aprotic solvent and an electrically conductive salt, and (c) a counterelectrode. 5 figs.

  9. Chemically modified graphite for electrochemical cells

    DOE Patents [OSTI]

    Greinke, R.A.; Lewis, I.C.

    1998-05-26

    This invention relates to chemically modified graphite particles: (a) that are useful in alkali metal-containing electrode of a electrochemical cell comprising: (1) the electrode, (2) a non-aqueous electrolytic solution comprising an organic aprotic solvent which solvent tends to decompose when the electrochemical cell is in use, and an electrically conductive salt of an alkali metal, and (3) a counter electrode; and (b) that are chemically modified with fluorine, chlorine, iodine or phosphorus to reduce such decomposition. This invention also relates to electrodes comprising such chemically modified graphite and a binder and to electrochemical cells containing such electrodes. 3 figs.

  10. Structured copolymers and their use as absorbents, gels and carriers of metal ions

    DOE Patents [OSTI]

    Hedstrand, David M.; Helmer, Bradley J.; Tomalia, Donald A.

    1996-01-01

    Dense star polymers or dendrimers having a highly branched interior structure capable of associating or chelating with metal ions are modified by capping with a hydrophobic group capable of providing a hydrophobic outer shell. The modified dendrimers are useful for dispersing metal ions in a non-aqueous polymer matrix. Also dense star polymers or dendrimers having a highly branched hydrophilic interior structure are modified by capping with a hydrophobic group capable of providing a hydrophobic outer shell, which modified polymers are useful as gels and surfactants.

  11. Structured copolymers and their use as absorbents, gels and carriers of metal ions

    DOE Patents [OSTI]

    Hedstrand, D.M.; Helmer, B.J.; Tomalia, D.A.

    1996-10-01

    Dense star polymers or dendrimers having a highly branched interior structure capable of associating or chelating with metal ions are modified by capping with a hydrophobic group capable of providing a hydrophobic outer shell. The modified dendrimers are useful for dispersing metal ions in a non-aqueous polymer matrix. Also dense star polymers or dendrimers having a highly branched hydrophilic interior structure are modified by capping with a hydrophobic group capable of providing a hydrophobic outer shell, which modified polymers are useful as gels and surfactants.

  12. Dynamic Underground Stripping: In situ steam sweeping and electrical heating to remediate a deep hydrocarbon spill

    SciTech Connect (OSTI)

    Yow, J.L. Jr.; Aines, R.D.; Newmark, R.L.; Udell, K.S.; Ziagos, J.P.

    1994-07-01

    Dynamic Underground Stripping is a combination of in situ steam injection, electrical resistance heating, and fluid extraction for rapid removal and recovery of subsurface contaminants such as solvents or fuels. Underground imaging and other measurement techniques monitor the system in situ for process control. Field tests at a deep gasoline spill at Lawrence Livermore National Laboratory recovered over 7000 gallons of gasoline during several months of field operations. Preliminary analysis of system cost and performance indicate that Dynamic Underground Stripping compares favorably with conventional pump-and-treat and vacuum extraction schemes for removing non-aqueous phase liquids such as gasoline from deep subsurface plumes.

  13. Electrolytic orthoborate salts for lithium batteries

    DOE Patents [OSTI]

    Angell, Charles Austen; Xu, Wu

    2008-01-01

    Orthoborate salts suitable for use as electrolytes in lithium batteries and methods for making the electrolyte salts are provided. The electrolytic salts have one of the formulae (I). In this formula anionic orthoborate groups are capped with two bidentate chelating groups, Y1 and Y2. Certain preferred chelating groups are dibasic acid residues, most preferably oxalyl, malonyl and succinyl, disulfonic acid residues, sulfoacetic acid residues and halo-substituted alkylenes. The salts are soluble in non-aqueous solvents and polymeric gels and are useful components of lithium batteries in electrochemical devices.

  14. Electrolytic orthoborate salts for lithium batteries

    DOE Patents [OSTI]

    Angell, Charles Austen [Mesa, AZ; Xu, Wu [Tempe, AZ

    2009-05-05

    Orthoborate salts suitable for use as electrolytes in lithium batteries and methods for making the electrolyte salts are provided. The electrolytic salts have one of the formulae (I). In this formula anionic orthoborate groups are capped with two bidentate chelating groups, Y1 and Y2. Certain preferred chelating groups are dibasic acid residues, most preferably oxalyl, malonyl and succinyl, disulfonic acid residues, sulfoacetic acid residues and halo-substituted alkylenes. The salts are soluble in non-aqueous solvents and polymeric gels and are useful components of lithium batteries in electrochemical devices.

  15. Cathode architectures for alkali metal / oxygen batteries

    SciTech Connect (OSTI)

    Visco, Steven J; Nimon, Vitaliy; De Jonghe, Lutgard C; Volfkovich, Yury; Bograchev, Daniil

    2015-01-13

    Electrochemical energy storage devices, such as alkali metal-oxygen battery cells (e.g., non-aqueous lithium-air cells), have a cathode architecture with a porous structure and pore composition that is tailored to improve cell performance, especially as it pertains to one or more of the discharge/charge rate, cycle life, and delivered ampere-hour capacity. A porous cathode architecture having a pore volume that is derived from pores of varying radii wherein the pore size distribution is tailored as a function of the architecture thickness is one way to achieve one or more of the aforementioned cell performance improvements.

  16. Method for digesting a nitro-bearing explosive compound

    DOE Patents [OSTI]

    Shah, Manish M.

    2000-01-01

    The present invention is a process wherein superoxide radicals from superoxide salt are used to break down the explosive compounds. The process has an excellent reaction rate for degrading explosives, and operates at ambient temperature and atmospheric pressure in aqueous or non-aqueous conditions. Because the superoxide molecules are small, much smaller than an enzyme molecule for example, they can penetrate the microstructure of plastic explosives faster. The superoxide salt generates reactive hydroxyl radicals, which can destroy other organic contaminants, if necessary, along with digesting the explosive nitro-bearing compound.

  17. Preparation and characterization of Pd{sub 2}Sn nanoparticles

    SciTech Connect (OSTI)

    Page, Katharine; Schade, Christina S.; Zhang, Jinping; Chupas, Peter J.; Chapman, Karena W.; Proffen, Thomas; Cheetham, Anthony K.; Seshadri, Ram

    2007-12-04

    We report a non-aqueous solution preparation of Pd{sub 2}Sn nanoparticles with sizes near 20 nm. The intermetallic compound with the Co{sub 2}Si structure has been characterized using transmission electron microscopy, Rietveld refinement of synchrotron X-ray and neutron powder diffraction, and real-space pair distribution function analysis of high-energy synchrotron X-ray scattering. We also present a description of the electronic structure of this covalent intermetallic using density functional calculations of the electronic structure.

  18. Chemically modified graphite for electrochemical cells

    DOE Patents [OSTI]

    Greinke, Ronald Alfred (Medina, OH); Lewis, Irwin Charles (Strongsville, OH)

    1998-01-01

    This invention relates to chemically modified graphite particles: (a) that are useful in alkali metal-containing electrode of a electrochemical cell comprising: (i) the electrode, (ii) a non-aqueous electrolytic solution comprising an organic aprotic solvent which solvent tends to decompose when the electrochemical cell is in use, and an electrically conductive salt of an alkali metal, and (iii) a counterelectrode; and (b) that are chemically modified with fluorine, chlorine, iodine or phosphorus to reduce such decomposition. This invention also relates to electrodes comprising such chemically modified graphite and a binder and to electrochemical cells containing such electrodes.

  19. Superfund record of decision (EPA Region 8): Smeltertown Site, Operable Unit 2, former Koppers Wood Treating site, Salida, CO, June 4, 1998

    SciTech Connect (OSTI)

    1998-10-01

    This decision document presents the selected remedial action (RA) for the former Koppers Wood Treating Operable Unit (OU2) at the Smeltertown Superfund Site (the Site). This action addresses the wood-treating contaminants from the tie treating operations at the former Koppers Wood Treating Operable Unit that were conducted by Koppers Company, Inc. (now known as Beazer East, Inc.) from 1924 through 1953. This remedy calls for the containment of soils contaminated at low levels and monitors the effect of the contaminants in the soils, dissolved polycyclic aromatic hydrocarbon (PAHs) and dense non-aqueous phase liquids (DNAPL) within the groundwater.

  20. Lithium metal oxide electrodes for lithium cells and batteries

    DOE Patents [OSTI]

    Thackeray, Michael M.; Johnson, Christopher S.; Amine, Khalil; Kim, Jaekook

    2006-11-14

    A lithium metal oxide positive electrode for a non-aqueous lithium cell is disclosed. The cell is prepared in its initial discharged state and has a general formula xLiMO.sub.2.(1-x)Li.sub.2M'O.sub.3 in which 0

  1. Long life lithium batteries with stabilized electrodes

    DOE Patents [OSTI]

    Amine, Khalil; Liu, Jun; Vissers, Donald R.; Lu, Wenquan

    2009-03-24

    The present invention relates to non-aqueous electrolytes having electrode stabilizing additives, stabilized electrodes, and electrochemical devices containing the same. Thus the present invention provides electrolytes containing an alkali metal salt, a polar aprotic solvent, and an electrode stabilizing additive. In some embodiments the additives include a substituted or unsubstituted cyclic or spirocyclic hydrocarbon containing at least one oxygen atom and at least one alkenyl or alkynyl group. When used in electrochemical devices with, e.g., lithium manganese oxide spinel electrodes or olivine or carbon-coated olivine electrodes, the new electrolytes provide batteries with improved calendar and cycle life.

  2. Lithium metal oxide electrodes for lithium cells and batteries

    DOE Patents [OSTI]

    Thackeray, Michael M.; Johnson, Christopher S.; Amine, Khalil; Kim, Jaekook

    2004-01-13

    A lithium metal oxide positive electrode for a non-aqueous lithium cell is disclosed. The cell is prepared in its initial discharged state and has a general formula xLiMO.sub.2.(1-x)Li.sub.2 M'O.sub.3 in which 0

  3. Transport, Targeting, and Applications of Metallic Functional Nanoparticles for Degradation of DNAPL Chlorinated Organic Solvents

    SciTech Connect (OSTI)

    Gregory V. Lowry; Sara Majetich; Krzysztof Matyjaszewski; David Sholl; Robert Tilton

    2006-12-27

    Dense Non-Aqueous Phase Liquid (DNAPL) such as trichloroethylene act as long term sources of groundwater contaminants and are difficult and expensive to remediate. DNAPL-contaminated sites are a significant financial liability for the Department of Energy and the private sector. The objective of this study was to engineer reactive Fe-based nanoparticles with specialized polymeric coatings to make them mobile in the subsurface and to provide them with an affinity for the DNAPL/water interface. The synthesis, characterization, and reactivity/mobility of the engineered particles, and a molecular dynamic model that predicts their behavior at the DNPAL/water interface are described in this report.

  4. self-concentrating-amine | netl.doe.gov

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

    Post-Combustion CO2 Capture for Existing PC Boilers by Self-concentrating Amine Absorbent Project No.: DE-FE0004274 3H Company will evaluate the feasibility of its "Self-Concentrating Absorbent CO2 Capture Process." The process is based on amines in a non-aqueous solvent which, upon reaction with CO2, separate into two distinct phases: a CO2-rich liquid phase and a dilute lean phase. The proposed process offers several potential advantages. Preliminary experimental data show that the

  5. Anodes for rechargeable lithium batteries

    DOE Patents [OSTI]

    Thackeray, Michael M.; Kepler, Keith D.; Vaughey, John T.

    2003-01-01

    A negative electrode (12) for a non-aqueous electrochemical cell (10) with an intermetallic host structure containing two or more elements selected from the metal elements and silicon, capable of accommodating lithium within its crystallographic host structure such that when the host structure is lithiated it transforms to a lithiated zinc-blende-type structure. Both active elements (alloying with lithium) and inactive elements (non-alloying with lithium) are disclosed. Electrochemical cells and batteries as well as methods of making the negative electrode are disclosed.

  6. 2,5-Dimethoxy-1,4-Benzoquinone (DMBQ) as Organic Cathode for Rechargeable

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

    Magnesium-Ion Batteries - Joint Center for Energy Storage Research January 13, 2016, Research Highlights 2,5-Dimethoxy-1,4-Benzoquinone (DMBQ) as Organic Cathode for Rechargeable Magnesium-Ion Batteries Image for Organic Cathode Scientific Achievement 2,5-dimethoxyl-1,4-benzoquinone (DMBQ) was investigated as 2 V (vs Mg/Mg2+) organic cathode material for non-aqueous rechargeable magnesium-ion batteries Significance and Impact Mg-DMBQ batteries were demonstrated to work with a discharge

  7. International Nuclear Energy Research Initiative Development of Computational Models for Pyrochemical Electrorefiners of Nuclear Waste Transmutation Systems

    SciTech Connect (OSTI)

    M.F. Simpson; K.-R. Kim

    2010-12-01

    In support of closing the nuclear fuel cycle using non-aqueous separations technology, this project aims to develop computational models of electrorefiners based on fundamental chemical and physical processes. Spent driver fuel from Experimental Breeder Reactor-II (EBR-II) is currently being electrorefined in the Fuel Conditioning Facility (FCF) at Idaho National Laboratory (INL). And Korea Atomic Energy Research Institute (KAERI) is developing electrorefining technology for future application to spent fuel treatment and management in the Republic of Korea (ROK). Electrorefining is a critical component of pyroprocessing, a non-aqueous chemical process which separates spent fuel into four streams: (1) uranium metal, (2) U/TRU metal, (3) metallic high-level waste containing cladding hulls and noble metal fission products, and (4) ceramic high-level waste containing sodium and active metal fission products. Having rigorous yet flexible electrorefiner models will facilitate process optimization and assist in trouble-shooting as necessary. To attain such models, INL/UI has focused on approaches to develop a computationally-light and portable two-dimensional (2D) model, while KAERI/SNU has investigated approaches to develop a computationally intensive three-dimensional (3D) model for detailed and fine-tuned simulation.

  8. Corrosion, passivity and breakdown of alloys used in high energy density batteries: Final report

    SciTech Connect (OSTI)

    Kruger, J.

    1987-10-01

    The objective of this research is to further the understanding of the passivity of metals and alloys in non-aqueous and mixed solvents. There is a lack of data in this area, despite its importance to applications such as the construction materials for high energy density batteries. There have been a number of corrosion-related problems reported in the construction materials of such batteries. As demands for longevity for these batteries increase, problems associated with corrosion will become increasingly important. This work is concerned with analyzing the nature, mode of formation, and mode of breakdown of passive films that exist on alloys in non-aqueous and mixed solvents. Work during Year I has concentrated upon generating cyclic voltammograms and potentiodynamic curves as baseline data on Au and Armco Fe in water/propylene carbonate mixtures. In addition, Scanning Electron Microscopy has been performed in order to characterize the attack observed and to correlate it to the electrochemical parameters measured. 3 refs., 15 figs.

  9. Magnetoreological Fluid Template for Basic Studies of Mechanical-Chemical Effects During Polishing

    SciTech Connect (OSTI)

    Miao, C.; Bristol, K. M.; Marino, A.E.; Shafrir, S.N.; DeGroote, J.E.; Jacobs, S.D.

    2008-01-07

    We developed a new magnetorheological (MR) fluid for studying the relative contributions of mechanics and chemistry in polishing hard materials. The base carrier fluid is a mixture of two non-aqueous liquids. At conventional carbonyl iron (CI) magnetic particle concentrations, removal rates with this formulation were unacceptably low for the polycrystalline optical ceramic aluminum oxynitride (ALON). We overcame this problem by creating a high magnetic solids concentration suspension consisting of blend of large and small CI particles. Our test bed for experiments was a magnetorheological finishing (MRF) spot-taking machine (STM) that can only polish spots into a non-rotating part. We demonstrated that, using this new MR fluid formation, we could substantially increase peak removal rates on ALON with small additions of nonmagnetic, nanodiamond abrasives. Material removal with this fluid was assumed to be predominately driven by mechanics. With the addition of small amounts of DI water to the base fluid containing nanodiamonds, the peak removal rate showed an additional increase, presumably due to the altered fluid rheology and possibly chemical interactions. In this paper we describe the difficult fluid viscosity issues that were addressed in creating a viable, high removal rate, non-aqueous MR fluid template that could be pumped in the STM for several days of experiments.

  10. Preparation of hydrophobic organic aeorgels

    DOE Patents [OSTI]

    Baumann, Theodore F.; Satcher, Jr., Joe H.; Gash, Alexander E.

    2007-11-06

    Synthetic methods for the preparation of hydrophobic organics aerogels. One method involves the sol-gel polymerization of 1,3-dimethoxybenzene or 1,3,5-trimethoxybenzene with formaldehyde in non-aqueous solvents. Using a procedure analogous to the preparation of resorcinol-formaldehyde (RF) aerogels, this approach generates wet gels that can be dried using either supercritical solvent extraction to generate the new organic aerogels or air dried to produce an xerogel. Other methods involve the sol-gel polymerization of 1,3,5 trihydroxy benzene (phloroglucinol) or 1,3 dihydroxy benzene (resorcinol) and various aldehydes in non-aqueous solvents. These methods use a procedure analogous to the one-step base and two-step base/acid catalyzed polycondensation of phloroglucinol and formaldehyde, but the base catalyst used is triethylamine. These methods can be applied to a variety of other sol-gel precursors and solvent systems. These hydrophobic organics aerogels have numerous application potentials in the field of material absorbers and water-proof insulation.

  11. Preparation of hydrophobic organic aeorgels

    DOE Patents [OSTI]

    Baumann, Theodore F.; Satcher, Jr., Joe H.; Gash, Alexander E.

    2004-10-19

    Synthetic methods for the preparation of hydrophobic organics aerogels. One method involves the sol-gel polymerization of 1,3-dimethoxybenzene or 1,3,5-trimethoxybenzene with formaldehyde in non-aqueous solvents. Using a procedure analogous to the preparation of resorcinol-formaldehyde (RF) aerogels, this approach generates wet gels that can be dried using either supercritical solvent extraction to generate the new organic aerogels or air dried to produce an xerogel. Other methods involve the sol-gel polymerization of 1,3,5 trihydroxy benzene (phloroglucinol) or 1,3 dihydroxy benzene (resorcinol) and various aldehydes in non-aqueous solvents. These methods use a procedure analogous to the one-step base and two-step base/acid catalyzed polycondensation of phloroglucinol and formaldehyde, but the base catalyst used is triethylamine. These methods can be applied to a variety of other sol-gel precursors and solvent systems. These hydrophobic organics aerogels have numerous application potentials in the field of material absorbers and water-proof insulation.

  12. SYNTHESIS OF A NEW FAMILY OF FLUORINATED BORONATE COMPOUNDS AS ANION RECEPTORS AND STUDIES OF THEIR USE AS ADDITIVES IN LITHIUM BATTERY ELECTROLYTES.

    SciTech Connect (OSTI)

    MCBREEN,J.; LEE,H.S.; YANG,X.Q.

    2001-06-08

    Numerous studies have been done on developing new electrolytes for lithium batteries with high ionic conductivity, and good chemical and electrochemical stability. In addition to the research on new salts and solvents, the use of cation receptors to reduce ion pairing in non-aqueous electrolytes has been considered as an approach to improve the properties of electrolytes. Although both cation and anion receptors enhance the dissociation of ion pairs and increase the conductivity of electrolytes, the use of anion receptors is more attractive for a lithium battery electrolyte because anion receptors increase the lithium transference number in the electrolyte. However, most available neutral anion receptors complex with anions through hydrogen binding and cannot be used in lithium batteries. Recently, we have reported on synthesis of a series of new neutral boron compounds as anion receptors based on the idea that electron-deficient boron would complex the anion of the ion pair. The anion complexation effect of these boron compounds was further enhanced by attaching electron-withdrawing groups. Here we report synthesis of another new family of boronate compounds. The effect of these new compounds on conductivity of lithium salts in non-aqueous solution was studied. The molecular weights of these new boronate compounds are lower than our previously reported boron compounds. Therefore, their effects on conductivity enhancement are superior. They also display high electrochemical stability up to 5 V.

  13. Leaching of BTEX from Aged Crude Oil Contaminated Model Soils: Experimental and Modeling Results

    SciTech Connect (OSTI)

    Huesemann, Michael H.; Hausmann, Tom S.; Fortman, Timothy J.

    2005-01-01

    It is generally assumed that soil properties such as organic matter content, porosity, and mineral surface area have a significant effect on the bioavailability and leachability of aged petroleum hydrocarbons. In order to test this hypothesis, nine model soils or sorbents (i.e., fine and coarse quartz sand, montmorillonite and kaolinite clay, peat, 60? and 150? silica gel, a loam soil, and non-porous glass beads) were spiked with a crude oil, aged for 27 months in the laboratory, and transferred to glass columns for the performance of continuous flow leaching experiments. The column effluents were periodically sampled for 43 days and analyzed for BTEX. A one-dimensional flow model for predicting the dissolution and dispersion of individual hydrocarbons from a multi-component NAPL such as crude oil was used to fit the leaching data (i.e., the BTEX concentration versus time curves) by adjusting the equilibrium oil-leachate partitioning coefficient (Kol) for each respective hydrocarbon. The Peclet number, which is a measure of dispersion and a required modeling parameter, was measured in separate chloride tracer experiments for each soil column. Results demonstrate that soil properties did not significantly affect the leaching kinetics of BTEX from the columns. Instead, BTEX leaching curves could be successfully fitted with the one-dimensional NAPL dissolution flow model for all sorbents with the exception of montmorillonite clay. The fitting parameter Kol for each hydrocarbon was found to be similar to the Kol values that were independently measured for the same crude oil by Rixey et al. (Journal of Hazardous Materials B, 65: 137-156, 1999). In addition, the fitted Kol values were very similar for BTEX leaching from aged compared to freshly spiked loam soil. These findings indicate that leaching of BTEX in the aged soils that are contaminated with crude oil at the high concentrations commonly found in the environment (i.e., >20,000 mg/kg) was not affected by soil

  14. Superfund record of decision amendment (EPA Region 2): Hooker (102nd Street Landfill), Niagara Falls, NY, June 9, 1995

    SciTech Connect (OSTI)

    1995-08-01

    This decision document presents the selected modification to the original remedial action (PB91-921417) for the 102nd Street Landfill Site (the `Site`), located in Niagara Falls, New York. The modification to the selected remedy addresses the river sediments within the shallow embayment of the Niagara River adjacent to the Site. The major components of the modification to the selected remedy include: dredging the Niagara River sediments to the `clean line` with respect to Site-related contamination. These sediments, after dewatering, will NOT be incinerated, but will be consolidated on the landfill. Any NAPL found within these sediments will be extracted, and will be incinerated at an off-site facility.

  15. T2VOC user`s guide

    SciTech Connect (OSTI)

    Falta, R.W.; Pruess, K.; Finsterle, S.; Battistelli, A.

    1995-03-01

    T2VOC is a numerical simulator for three-phase, three-component, non-isothermal flow of water, air, and a volatile organic compound (VOC) in multidimensional heterogeneous porous media. Developed at the Lawrence Berkeley Laboratory, T2VOC is an extension of the TOUGH2 general-purpose simulation program. This report is a self-contained guide to application of T2VOC to subsurface contamination problems involving nonaqueous phase liquids (NAPLs). It gives a technical description of the T2VOC code, including a discussion of the physical processes modeled, and the mathematical and numerical methods used. Detailed instructions for preparing input data are presented along with several illustrative sample problems.

  16. Spatial decision support for strategic environmental assessment of land use plans. A case study in southern Italy

    SciTech Connect (OSTI)

    Geneletti, Davide . E-mail: davide.geneletti@ing.unitn.it; Bagli, Stefano . E-mail: home@gecosistema.it; Napolitano, Paola . E-mail: home@gecosistema.it

    2007-07-15

    This paper presents and discusses the construction of a spatial decision-support tool for the Strategic Environmental Assessment (SEA) of a land use plan: the spatial coordination plan of the Province of Naples, in southern Italy. The decision-support tool organises the relevant information, spatially resolves the actions of the plan, predicts their environmental impacts, and generates overall performance maps. Its final goal is to provide a suitable technical support to a formal SEA procedure. The expected implications of the plan, such as changes in land use and traffic flows and urban expansion, were modelled and assessed against a set of environmental criteria using SWOT (Strengths, Weaknesses, Opportunities and Threats) analysis and mapping. It was found that the SWOT analysis provided a good basis for assessment and strategy formulation. The paper also intends to contribute to the topic of data and scale issues in SEA, by exemplifying the role played by spatial data and spatial analyses to support informative SEA.

  17. sup 40 Ar- sup 39 Ar and K-Ar dating of K-rich rocks from the Roccamonfina volcano, Roman Comagmatic Region, Italy

    SciTech Connect (OSTI)

    Di Brozolo, F.R.; Di Girolamo, P.; Turi, B.; Oddone, M. )

    1988-06-01

    Roccamonfina is the northernmost Volcano of the Campanian area of the K-rich Roman comagmatic Region of Italy. It erupted a huge amount of pyroclastics and lavas belonging to both the Leucite-Basanite and Leucitite Series (LBLS) and the Shoshonite Series (SS), spread over an area of about 300 km{sup 2}. The above series correspond to the High-K Series (HKS) and Low-K Series (LKS) of Appleton (1971), respectively. {sup 40}Ar-{sup 39}Ar and K-Ar dating of samples from both series gave ages ranging from 0.656 to 0.096 Ma for the SS and from 1.03( ) to 0.053 Ma for the LBLS. These results indicate that the products of the two series were outpoured together at least between 0.7 and 0.1 Ma age, i.e. during both the so-called pre-caldera phase and the post-caldera phase of activity. The latest products of the volcanism at Roccamonfina were erupted just before the deposition of the Grey Campanian Ignimbrite, which erupted from vents located about 50 km to the south in the Phlegrean Fields near Naples and has an age of about 33,000 years. Taking into account all the available all the available radiometric data the authors conclude that Roccamonfina was active between 1.5 and 0.05 Ma ago, in excellent agreement with the stratigraphic evidence. In this same time span is concentrated the activity of all the centers of the Roman Region north of Naples.

  18. Preferential solvation of lithium cations and impacts on oxygen reduction in lithium–air batteries

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

    Zheng, Dong; Qu, Deyu; Yang, Xiao -Qing; Lee, Hung -Sui; Qu, Deyang

    2015-09-16

    The solvation of Li⁺ with eleven non-aqueous solvents commonly used as the electrolytes for Li batteries were studied. The solvation preferences of different solvents were compared by means of electrospray mass spectrometry and collision-induced dissociation. The relative strength of the solvent for the solvation of Li⁺ was determined. The Lewis acidity of the solvated Li⁺ cations was determined by the preferential solvation of the solvent in the solvation shell. The kinetics of the catalytic disproportionation of the O₂⁻ depends on the relative Lewis acidity of the solvated Li⁺ ion. The impact of the solvated Li⁺ cation on the O₂ redoxmore » reaction was also investigated.« less

  19. Analyzing remediation technologies for Department of Energy sites contaminated with DNAPL pollutants. Master`s thesis

    SciTech Connect (OSTI)

    Papatyi, A.F.

    1997-03-01

    The Department of Energy is in the process of conducting a Remedial Investigation/Feasibility Study for a site contaminated with Dense Non-Aqueous Phase Liquid (DNAPL) pollutants at their Paducah Kentucky facility. This thesis effort focuses on acquiring insight into a number of remediation technology trains that are candidates for the Paducah site. This insight is used to recommend and justify the screening of candidate technology trains. The research makes use of two decision analysis models (one is deterministic, the other is probabilistic) built to provide a quantitative assessment of the candidate technology trains. Dominance considerations and multi-attribute utility theory are utilized to make the quantitative assessments and to gain insight into each candidate technology train. The results of the analysis provide the DOE with a rational justification for screening 55 of the 58 candidate technology trains from further consideration.

  20. New capabilities and applications for electrophoretically deposited coatings

    SciTech Connect (OSTI)

    Sharp, D.J.

    1991-01-01

    Our primary purpose in this test is to provide a brief general description of a few applications of various electrophoretic systems which have been investigated and have found use in various coating applications at Sandia National Laboratories. Both organic and inorganic suspensions in aqueous and non-aqueous media have been considered in these studies. Applications include high voltage insulating dielectrics, thermally conductive/electrically insulating films, adherent lubricating films, uniform photoresist films, glass coatings, and fissile uranium oxide/carbon composite films for studies of nuclear powered lasers. More recently, we have become interested in the beneficial environmental aspects of being able to provide protective polymer coatings which reduce or minimize the use of organic solvents required by traditional spray coat processes. Important practical factors which relate to film uniformity, adhesion, and composition are related to unique coating or plating capabilities and applications. 6 refs., 2 figs., 1 tab.

  1. Process to produce lithium-polymer batteries

    DOE Patents [OSTI]

    MacFadden, Kenneth Orville

    1998-01-01

    A polymer bonded sheet product suitable for use as an electrode in a non-aqueous battery system. A porous electrode sheet is impregnated with a solid polymer electrolyte, so as to diffuse into the pores of the electrode. The composite is allowed to cool, and the electrolyte is entrapped in the porous electrode. The sheet products composed have the solid polymer electrolyte composition diffused into the active electrode material by melt-application of the solid polymer electrolyte composition into the porous electrode material sheet. The solid polymer electrolyte is maintained at a temperature that allows for rapid diffusion into the pores of the electrode. The composite electrolyte-electrode sheets are formed on current collectors and can be coated with solid polymer electrolyte prior to battery assembly. The interface between the solid polymer electrolyte composite electrodes and the solid polymer electrolyte coating has low resistance.

  2. Process to produce lithium-polymer batteries

    DOE Patents [OSTI]

    MacFadden, K.O.

    1998-06-30

    A polymer bonded sheet product is described suitable for use as an electrode in a non-aqueous battery system. A porous electrode sheet is impregnated with a solid polymer electrolyte, so as to diffuse into the pores of the electrode. The composite is allowed to cool, and the electrolyte is entrapped in the porous electrode. The sheet products composed have the solid polymer electrolyte composition diffused into the active electrode material by melt-application of the solid polymer electrolyte composition into the porous electrode material sheet. The solid polymer electrolyte is maintained at a temperature that allows for rapid diffusion into the pores of the electrode. The composite electrolyte-electrode sheets are formed on current collectors and can be coated with solid polymer electrolyte prior to battery assembly. The interface between the solid polymer electrolyte composite electrodes and the solid polymer electrolyte coating has low resistance. 1 fig.

  3. Electrode for a lithium cell

    DOE Patents [OSTI]

    Thackeray, Michael M.; Vaughey, John T.; Dees, Dennis W.

    2008-10-14

    This invention relates to a positive electrode for an electrochemical cell or battery, and to an electrochemical cell or battery; the invention relates more specifically to a positive electrode for a non-aqueous lithium cell or battery when the electrode is used therein. The positive electrode includes a composite metal oxide containing AgV.sub.3O.sub.8 as one component and one or more other components consisting of LiV.sub.3O.sub.8, Ag.sub.2V.sub.4O.sub.11, MnO.sub.2, CF.sub.x, AgF or Ag.sub.2O to increase the energy density of the cell, optionally in the presence of silver powder and/or silver foil to assist in current collection at the electrode and to improve the power capability of the cell or battery.

  4. Electrochemical Processing of Used Nuclear Fuel

    SciTech Connect (OSTI)

    K. M. Goff; J. C. Wass; G. M. Teske

    2011-08-01

    As part of the Department of Energys Fuel Cycle Research and Development Program an electrochemical technology employing molten salts is being developed for recycle of metallic fast reactor fuel and treatment of light water reactor oxide fuel to produce a feed for fast reactors. This technology has been deployed for treatment of used fuel from the Experimental Breeder Reactor II (EBR-II) in the Fuel Conditioning Facility, located at the Materials and Fuel Complex of Idaho National Laboratory. This process is based on dry (non-aqueous) technologies that have been developed and demonstrated since the 1960s. These technologies offer potential advantages compared to traditional aqueous separations including: compactness, resistance to radiation effects, criticality control benefits, compatibility with advanced fuel types, and ability to produce low purity products. This paper will summarize the status of electrochemical development and demonstration activities with used nuclear fuel, including preparation of associated high-level waste forms.

  5. Anion-tunable properties and electrochemical performance of functionalized ferrocene compounds

    SciTech Connect (OSTI)

    Cosimbescu, Lelia; Wei, Xiaoliang; Vijayakumar, M.; Xu, Wu; Helm, Monte L.; Burton, Sarah D.; Sorensen, Christina M.; Liu, Jun; Sprenkle, Vincent; Wang, Wei

    2015-09-16

    We report a series of ionically modified ferrocene compounds for hybrid lithium-organic non-aqueous redox flow batteries, based on the ferrocene/ferrocenium redox couple as the active catholyte material. Tetraalkylammonium ionic moieties were incorporated into the ferrocene structure, in order to enhance the solubility of the otherwise relatively insoluble ferrocene. The effect of various counter anions of the tetraalkylammonium ionized species appended to the ferrocene, such as bis(trifluoromethanesulfonyl)imide, hexafluorophosphate, perchlorate, tetrafluoroborate, and dicyanamide on the solubility of the ferrocene was investigated. The solution chemistry of the ferrocene species was studied, in order to understand the mechanism of solubility enhancement. Lastly, the electrochemical performance of these ionized ferrocene species was evaluated and shown to have excellent cell efficiency and superior cycling stability.

  6. Lithium metal oxide electrodes for lithium batteries

    DOE Patents [OSTI]

    Thackeray, Michael M.; Kim, Jeom-Soo; Johnson, Christopher S.

    2008-01-01

    An uncycled electrode for a non-aqueous lithium electrochemical cell including a lithium metal oxide having the formula Li.sub.(2+2x)/(2+x)M'.sub.2x/(2+x)M.sub.(2-2x)/(2+x)O.sub.2-.delta., in which 0.ltoreq.x<1 and .delta. is less than 0.2, and in which M is a non-lithium metal ion with an average trivalent oxidation state selected from two or more of the first row transition metals or lighter metal elements in the periodic table, and M' is one or more ions with an average tetravalent oxidation state selected from the first and second row transition metal elements and Sn. Methods of preconditioning the electrodes are disclosed as are electrochemical cells and batteries containing the electrodes.

  7. Multi-component intermetallic electrodes for lithium batteries

    DOE Patents [OSTI]

    Thackeray, Michael M; Trahey, Lynn; Vaughey, John T

    2015-03-10

    Multi-component intermetallic negative electrodes prepared by electrochemical deposition for non-aqueous lithium cells and batteries are disclosed. More specifically, the invention relates to composite intermetallic electrodes comprising two or more compounds containing metallic or metaloid elements, at least one element of which can react with lithium to form binary, ternary, quaternary or higher order compounds, these compounds being in combination with one or more other metals that are essentially inactive toward lithium and act predominantly, but not necessarily exclusively, to the electronic conductivity of, and as current collection agent for, the electrode. The invention relates more specifically to negative electrode materials that provide an operating potential between 0.05 and 2.0 V vs. metallic lithium.

  8. Silver manganese oxide electrodes for lithium batteries

    DOE Patents [OSTI]

    Thackeray, Michael M.; Vaughey, John T.; Dees, Dennis W.

    2006-05-09

    This invention relates to electrodes for non-aqueous lithium cells and batteries with silver manganese oxide positive electrodes, denoted AgxMnOy, in which x and y are such that the manganese ions in the charged or partially charged electrodes cells have an average oxidation state greater than 3.5. The silver manganese oxide electrodes optionally contain silver powder and/or silver foil to assist in current collection at the electrodes and to improve the power capability of the cells or batteries. The invention relates also to a method for preparing AgxMnOy electrodes by decomposition of a permanganate salt, such as AgMnO4, or by the decomposition of KMnO4 or LiMnO4 in the presence of a silver salt.

  9. Investigation of the electrocatalytic oxygen reduction and evolution reactions in lithium–oxygen batteries

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

    Zheng, Dong; Zhang, Xuran; Qu, Deyu; Yang, Xiao -Qing; Lee, Hung -Sui; Qu, Deyang

    2015-04-21

    Oxygen reduction and oxygen evolution reactions were examined on graphite electrodes with different crystal orientations. The kinetics for the redox couple O2/O2•- are very fast, therefore no catalyst seems necessary to assist the charge transfer process. Apparently, the main source of the overpotential for the O2 reduction reaction is from mass diffusion. Li2O2 becomes soluble in non-aqueous electrolytes in the presence of the tetraethylammonium tetrafluoroborate additive. The soluble B-O22- ions can be oxidized electro-catalytically. The edge orientation of graphite demonstrates superior catalytic activity for the oxidation over basal orientation. The findings reveal an opportunity for recharging Li-air batteries efficiently andmore » a new strategy of developing the catalyst for oxygen evolution reaction.« less

  10. Lithium ion batteries based on nanoporous silicon

    SciTech Connect (OSTI)

    Tolbert, Sarah H.; Nemanick, Eric J.; Kang, Chris Byung-Hwa

    2015-09-22

    A lithium ion battery that incorporates an anode formed from a Group IV semiconductor material such as porous silicon is disclosed. The battery includes a cathode, and an anode comprising porous silicon. In some embodiments, the anode is present in the form of a nanowire, a film, or a powder, the porous silicon having a pore diameters within the range between 2 nm and 100 nm and an average wall thickness of within the range between 1 nm and 100 nm. The lithium ion battery further includes, in some embodiments, a non-aqueous lithium containing electrolyte. Lithium ion batteries incorporating a porous silicon anode demonstrate have high, stable lithium alloying capacity over many cycles.

  11. Room temperature, hybrid sodium-based flow batteries with multi-electron transfer redox reactions

    SciTech Connect (OSTI)

    Shamie, Jack S.; Liu, Caihong; Shaw, Leon L.; Sprenkle, Vincent L.

    2015-06-11

    We introduce a new concept of hybrid Na-based flow batteries (HNFBs) with a molten Na alloy anode in conjunction with a flowing catholyte separated by a solid Na-ion exchange membrane for grid-scale energy storage. Such HNFBs can operate at ambient temperature, allow catholytes to have multiple electron transfer redox reactions per active ion, offer wide selection of catholyte chemistries with multiple active ions to couple with the highly negative Na alloy anode, and enable the use of both aqueous and non-aqueous catholytes. Further, the molten Na alloy anode permits the decoupled design of power and energy since a large volume of the molten Na alloy can be used with a limited ion-exchange membrane size. In this proof-of-concept study, the feasibility of multielectron transfer redox reactions per active ion and multiple active ions for catholytes has been demonstrated. Furthermore, the critical barriers to mature this new HNFBs have also been explored.

  12. Anion-tunable properties and electrochemical performance of functionalized ferrocene compounds

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

    Cosimbescu, Lelia; Wei, Xiaoliang; Vijayakumar, M.; Xu, Wu; Helm, Monte L.; Burton, Sarah D.; Sorensen, Christina M.; Liu, Jun; Sprenkle, Vincent; Wang, Wei

    2015-09-16

    We report a series of ionically modified ferrocene compounds for hybrid lithium-organic non-aqueous redox flow batteries, based on the ferrocene/ferrocenium redox couple as the active catholyte material. Tetraalkylammonium ionic moieties were incorporated into the ferrocene structure, in order to enhance the solubility of the otherwise relatively insoluble ferrocene. The effect of various counter anions of the tetraalkylammonium ionized species appended to the ferrocene, such as bis(trifluoromethanesulfonyl)imide, hexafluorophosphate, perchlorate, tetrafluoroborate, and dicyanamide on the solubility of the ferrocene was investigated. The solution chemistry of the ferrocene species was studied, in order to understand the mechanism of solubility enhancement. Lastly, the electrochemicalmore » performance of these ionized ferrocene species was evaluated and shown to have excellent cell efficiency and superior cycling stability.« less

  13. Electrohydrodynamic atomization (EHDA) assisted wet chemical synthesis of nickel nanoparticles

    SciTech Connect (OSTI)

    Barzegar Vishlaghi, M. [Department of Mechanical Engineering, University of Tabriz, Tabriz (Iran, Islamic Republic of)] [Department of Mechanical Engineering, University of Tabriz, Tabriz (Iran, Islamic Republic of); Farzalipour Tabriz, M., E-mail: meisam.fa@gmail.com [Department of Mechanical Engineering, University of Tabriz, Tabriz (Iran, Islamic Republic of); Mohammad Moradi, O. [Department of Mechanical Engineering, University of Tabriz, Tabriz (Iran, Islamic Republic of)] [Department of Mechanical Engineering, University of Tabriz, Tabriz (Iran, Islamic Republic of)

    2012-07-15

    Highlights: ? Electrohydrodynamic atomization (EHDA) assisted chemical synthesis of nickel nanoparticles is reported. ? Substituting water with non-aqueous media prevents the formation of nickel hydroxide. ? Size of particles decreased from 10 to 20 nm down to 24 nm by using multi-jet mode. ? Synthesized nanoparticles have diffraction patterns similar to amorphous materials. -- Abstract: In this study nickel nanoparticles were prepared via chemical reduction of nickel acetate using sodium borohydride using electrohydrodynamic atomization (EHDA) technique. This technique was used to spray a finely dispersed aerosol of nickel precursor solution into the reductive bath. Obtained particles were characterized by means of X-ray diffraction (XRD), UVVisible spectroscopy, and transmission electron microscopy (TEM). Results confirmed the formation of nickel nanoparticles and showed that applying EHDA technique to chemical reduction method results in producing smaller particles with narrower size distribution in comparison with conventional reductive precipitation method.

  14. Room Temperature, Hybrid Sodium-Based Flow Batteries with Multi-Electron Transfer Redox Reactions

    SciTech Connect (OSTI)

    Shamie, Jack S.; Liu, Caihong; Shaw, Leon L.; Sprenkle, Vincent L.

    2015-06-11

    We introduce a new concept of hybrid Na-based flow batteries (HNFBs) with a molten Na alloy anode in conjunction with a flowing catholyte separated by a solid Na-ion exchange membrane for grid-scale energy storage. Such HNFBs can operate at ambient temperature, allow catholytes to have multiple electron transfer redox reactions per active ion, offer wide selection of catholyte chemistries with multiple active ions to couple with the highly negative Na alloy anode, and enable the use of both aqueous and non-aqueous catholytes. Further, the molten Na alloy anode permits the decoupled design of power and energy since a large volume of the molten Na alloy can be used with a limited ion-exchange membrane size. In this proof-of-concept study, the feasibility of multielectron transfer redox reactions per active ion and multiple active ions for catholytes has been demonstrated. The critical barriers to mature this new HNFBs have also been explored.

  15. Investigation of the electrocatalytic oxygen reduction and evolution reactions in lithiumoxygen batteries

    SciTech Connect (OSTI)

    Zheng, Dong; Zhang, Xuran; Qu, Deyu; Yang, Xiao -Qing; Lee, Hung -Sui; Qu, Deyang

    2015-04-21

    Oxygen reduction and oxygen evolution reactions were examined on graphite electrodes with different crystal orientations. The kinetics for the redox couple O2/O2- are very fast, therefore no catalyst seems necessary to assist the charge transfer process. Apparently, the main source of the overpotential for the O2 reduction reaction is from mass diffusion. Li2O2 becomes soluble in non-aqueous electrolytes in the presence of the tetraethylammonium tetrafluoroborate additive. The soluble B-O22- ions can be oxidized electro-catalytically. The edge orientation of graphite demonstrates superior catalytic activity for the oxidation over basal orientation. The findings reveal an opportunity for recharging Li-air batteries efficiently and a new strategy of developing the catalyst for oxygen evolution reaction.

  16. Health assessment for Hooker Chemical (102nd Street Landfill), Niagara Falls, New York, Region 2. CERCLIS No. NYD980506810. Preliminary report

    SciTech Connect (OSTI)

    Not Available

    1989-06-01

    The 102nd Street Landfill is two sites that comprise 22 acres. Occidental Chemical Corporation (OCC) and its predecessor, the Oldbury Electrochemical Company, deposited approximately 23,500 tons of mixed organic solvents, organic and inorganic phosphates, and related chemicals. Included in the site are approximately 300 tons of hexachlorocyclohexane process cake, including lindane. In addition, brine sludge, fly ash, electrochemical cell parts and related equipment in unknown quantities were dumped at the site. On-site contamination of the 102nd Street Landfill includes soils contaminated with non-aqueous phase liquids on both portions of the Landfill. Off-site contamination, based on current studies, results from contaminated ground-water leaching into the Niagara River which causes contamination of the river water, sediments, and aquatic organisms, including fish. The 102nd Street Landfill continues to represent a potential public health threat.

  17. Superfund Record of Decision (EPA Region 2): Hooker Chemical S-Area, Niagara Falls, NY. (First remedial action), September 1990. Final report

    SciTech Connect (OSTI)

    Not Available

    1990-09-21

    The Hooker Chemical S-Area site is a former landfill area located in Niagara Falls, New York. The site lies adjacent to the Niagara River. Approximately 63,000 tons of chemical processing wastes were disposed of at the landfill. Ground water beneath the site also has been contaminated from aqueous phase and non-aqueous phase liquid chemicals. Chemicals have migrated toward the Niagara Falls Drinking Water Treatment Plant (DWTP) which lies to the east of the site, contaminating the Bedrock intake structures. The Record of Decision (ROD) addresses the landfill, a contaminated ground water plume, bedrock contamination, and the DWTP. The primary contaminants of concern affecting the soil, sediment, and ground water are VOCs including PCE; and other organics including chlorinated organics and pesticides. The selected remedial action for the site is included.

  18. Solvent for urethane adhesives and coatings and method of use

    SciTech Connect (OSTI)

    Simandl, Ronald F.; Brown, John D.; Holt, Jerrid S.

    2010-08-03

    A solvent for urethane adhesives and coatings, the solvent having a carbaldehyde and a cyclic amide as constituents. In some embodiments the solvent consists only of miscible constituents. In some embodiments the carbaldehyde is benzaldehyde and in some embodiments the cyclic amide is N-methylpyrrolidone (M-pyrole). An extender may be added to the solvent. In some embodiments the extender is miscible with the other ingredients, and in some embodiments the extender is non-aqueous. For example, the extender may include isopropanol, ethanol, tetrahydro furfuryl alcohol, benzyl alcohol, Gamma-butyrolactone or a caprolactone. In some embodiments a carbaldehyde and a cyclic amide are heated and used to separate a urethane bonded to a component.

  19. Polymer concrete composites for the production of high strength pipe and linings in high temperature corrosive environments

    DOE Patents [OSTI]

    Zeldin, A.; Carciello, N.; Fontana, J.; Kukacka, L.

    High temperature corrosive resistant, non-aqueous polymer concrete composites are described. They comprise about 12 to 20% by weight of a water-insoluble polymer binder polymerized in situ from a liquid monomer mixture consisting essentially of about 40 to 70% by weight of styrene, about 25 to 45% by weight acrylonitrile and about 2.5 to 7.5% by weight acrylamide or methacrylamide and about 1 to 10% by weight of a crosslinking agent. This agent is selected from the group consisting of trimethylolpropane trimethacrylate and divinyl benzene; and about 80 to 88% by weight of an inert inorganic filler system containing silica sand and portland cement, and optionally Fe/sub 2/O/sub 3/ or carbon black or mica. A free radical initiator such as di-tert-butyl peroxide, azobisisobutyronitrile, benzoyl peroxide, lauryl peroxide, other organic peroxides and combinations thereof to initiate crosspolymerization of the monomer mixture in the presence of said inorganic filler.

  20. Anion-Tunable Properties and Electrochemical Performance of Functionalized Ferrocene Compounds

    SciTech Connect (OSTI)

    Cosimbescu, Lelia; Wei, Xiaoliang; Vijayakumar, M.; Xu, Wu; Helm, Monte L.; Burton, Sarah D.; Sorensen, Christina M.; Liu, Jun; Sprenkle, Vincent L.; Wang, Wei

    2015-09-01

    We report a series of ionically modified ferrocene compounds for hybrid lithium-organic non-aqueous redox flow batteries, based on the ferrocene/ferrocenium redox couple as the active catholyte material. Tetraalkylammonium ionic moieties were incorporated into the ferrocene structure, in order to enhance the solubility of the otherwise relatively insoluble ferrocene. The effect of various counter anions of the tetraalkylammonium ionized species appended to the ferrocene, such as bis(trifluoromethanesulfonyl)imide, hexafluorophosphate, perchlorate, tetrafluoroborate, and dicyanamide on the solubility of the ferrocene was investigated. The solution chemistry of the ferrocene species was studied, in order to understand the mechanism of solubility enhancement. Finally, the electrochemical performance of these ionized ferrocene species was evaluated and shown to have excellent cell efficiency and superior cycling stability.

  1. Preferential solvation of lithium cations and impacts on oxygen reduction in lithium–air batteries

    SciTech Connect (OSTI)

    Zheng, Dong; Qu, Deyu; Yang, Xiao -Qing; Lee, Hung -Sui; Qu, Deyang

    2015-09-16

    The solvation of Li⁺ with eleven non-aqueous solvents commonly used as the electrolytes for Li batteries were studied. The solvation preferences of different solvents were compared by means of electrospray mass spectrometry and collision-induced dissociation. The relative strength of the solvent for the solvation of Li⁺ was determined. The Lewis acidity of the solvated Li⁺ cations was determined by the preferential solvation of the solvent in the solvation shell. The kinetics of the catalytic disproportionation of the O₂⁻ depends on the relative Lewis acidity of the solvated Li⁺ ion. The impact of the solvated Li⁺ cation on the O₂ redox reaction was also investigated.

  2. Method for synthesizing pollucite from chabazite and cesium chloride

    DOE Patents [OSTI]

    Pereira, Candido

    1999-01-01

    A method for immobilizing waste chlorides salts containing radionuclides and hazardous nuclear material for permanent disposal, and in particular, a method for immobilizing waste chloride salts containing cesium, in a synthetic form of pollucite. The method for synthesizing pollucite from chabazite and cesium chloride includes mixing dry, non-aqueous cesium chloride with chabazite and heating the mixture to a temperature greater than the melting temperature of the cesium chloride, or above about 700.degree. C. The method further comprises significantly improving the rate of retention of cesium in ceramic products comprised of a salt-loaded zeolite by adding about 10% chabazite by weight to the salt-loaded zeolite prior to conversion at elevated temperatures and pressures to the ceramic composite.

  3. Method for synthesizing pollucite from chabazite and cesium chloride

    DOE Patents [OSTI]

    Pereira, C.

    1999-02-23

    A method is described for immobilizing waste chlorides salts containing radionuclides and hazardous nuclear material for permanent disposal, and in particular, a method is described for immobilizing waste chloride salts containing cesium, in a synthetic form of pollucite. The method for synthesizing pollucite from chabazite and cesium chloride includes mixing dry, non-aqueous cesium chloride with chabazite and heating the mixture to a temperature greater than the melting temperature of the cesium chloride, or above about 700 C. The method further comprises significantly improving the rate of retention of cesium in ceramic products comprised of a salt-loaded zeolite by adding about 10% chabazite by weight to the salt-loaded zeolite prior to conversion at elevated temperatures and pressures to the ceramic composite. 3 figs.

  4. Shell responses to state of Colorado comments on preliminary engineering design package for the shell section 36 trenches IRA. Volume 2

    SciTech Connect (OSTI)

    Not Available

    1990-12-19

    The Preliminary Engineering Package was to include: (1) An investigation and evaluation of different methods that could be utilized in investigating the dense non-aqueous phase liquid (DNAPL) found immediately downgradient of the Shell Section 36 Trenches, and descriptions of these techniques; (2) A discussion of the construction techniques (s) selected for emplacement of the containment wall, and any handling procedures applicable to that technique; Presentation of the monitoring network, sampling frequency, and a list of analytes to be included in the monitoring program. The purpose of presenting the Preliminary Engineering Design Package is to provide the Organizations and State with conceptual plan for implementing the IRA, as has been routinely done on other IRAs. Groundwater monitoring programs and construction techniques were being evaluated.

  5. Final decision document for other contamination sources, interim response action, shell section 36 trenches, RMA

    SciTech Connect (OSTI)

    1990-04-01

    The shell section 36 trenches were used from 1952 to 1966 for land disposal of liquid and solid wastes generated from pesticide manufacture. They have been shown to be a source of soil and ground water contamination for volatile and semivolatile compounds. A dense non-aqueous phase liquid (DNAPL) is also believed to have originated from the area. The objective of the interim response action is to reduce the lateral migration of contaminants emanating from the trenches. The preferred IRA alternative consists of (1) A physical barrier encircling the trenches and (2) a soil and vegetative cover to eliminate recharge. This final decision document provides summaries of: (1). Alternatives considered (2). Significant events leading to the initiation of the IRA (3). The IRA project (4). Applicable or relevant and appropriate requirements, standards.

  6. Anion-tunable properties and electrochemical performance of functionalized ferrocene compounds

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

    Cosimbescu, Lelia; Wei, Xiaoliang; Vijayakumar, M.; Xu, Wu; Helm, Monte L.; Burton, Sarah D.; Sorensen, Christina M.; Liu, Jun; Sprenkle, Vincent; Wang, Wei

    2015-09-16

    We report a series of ionically modified ferrocene compounds for hybrid lithium-organic non-aqueous redox flow batteries, based on the ferrocene/ferrocenium redox couple as the active catholyte material. Tetraalkylammonium ionic moieties were incorporated into the ferrocene structure, in order to enhance the solubility of the otherwise relatively insoluble ferrocene. The effect of various counter anions of the tetraalkylammonium ionized species appended to the ferrocene, such as bis(trifluoromethanesulfonyl)imide, hexafluorophosphate, perchlorate, tetrafluoroborate, and dicyanamide on the solubility of the ferrocene was investigated. The solution chemistry of the ferrocene species was studied, in order to understand the mechanism of solubility enhancement. Finally, the electrochemicalmoreperformance of these ionized ferrocene species was evaluated and shown to have excellent cell efficiency and superior cycling stability.less

  7. High temperature chemically resistant polymer concrete

    DOE Patents [OSTI]

    Sugama, T.; Kukacka, L.E.

    High temperature chemically resistant, non-aqueous polymer concrete composites consist of about 12 to 20% by weight of a water-insoluble polymer binder. The binder is polymerized in situ from a liquid vinyl-type monomer or mixture of vinyl containing monomers such as triallylcyanurate, styrene, acrylonitrile, acrylamide, methacrylamide, methyl-methacrylate, trimethylolpropane trimethacrylate and divinyl benzene. About 5 to 40% by weight of a reactive inorganic filler selected from the group consisting of tricalcium silicate and dicalcium silicate and mixtures containing less than 2% free lime, and about 48 to 83% by weight of silica sand/ and a free radical initiator such as di-tert-butyl peroxide, azobisisobutyronitrile, benzoyl peroxide, lauryl peroxide, other orgaic peroxides and combinations to initiate polymerization of the monomer in the presence of the inorganic filers are used.

  8. Redox shuttles for overcharge protection of lithium batteries

    DOE Patents [OSTI]

    Amine, Khalil; Chen, Zonghai; Wang, Qingzheng

    2010-12-14

    The present invention is generally related to electrolytes containing novel redox shuttles for overcharge protection of lithium-ion batteries. The redox shuttles are capable of thousands hours of overcharge tolerance and have a redox potential at about 3-5.5 V vs. Li and particularly about 4.4-4.8 V vs. Li. Accordingly, in one aspect the invention provides electrolytes comprising an alkali metal salt; a polar aprotic solvent; and a redox shuttle additive that is an aromatic compound having at least one aromatic ring with four or more electronegative substituents, two or more oxygen atoms bonded to the aromatic ring, and no hydrogen atoms bonded to the aromatic ring; and wherein the electrolyte solution is substantially non-aqueous. Further there are provided electrochemical devices employing the electrolyte and methods of making the electrolyte.

  9. Lithium-ion batteries with intrinsic pulse overcharge protection

    DOE Patents [OSTI]

    Chen, Zonghai; Amine, Khalil

    2013-02-05

    The present invention relates in general to the field of lithium rechargeable batteries, and more particularly relates to the positive electrode design of lithium-ion batteries with improved high-rate pulse overcharge protection. Thus the present invention provides electrochemical devices containing a cathode comprising at least one primary positive material and at least one secondary positive material; an anode; and a non-aqueous electrolyte comprising a redox shuttle additive; wherein the redox potential of the redox shuttle additive is greater than the redox potential of the primary positive material; the redox potential of the redox shuttle additive is lower than the redox potential of the secondary positive material; and the redox shuttle additive is stable at least up to the redox potential of the secondary positive material.

  10. Lithium Metal Oxide Electrodes For Lithium Cells And Batteries

    DOE Patents [OSTI]

    Thackeray, Michael M.; Johnson, Christopher S.; Amine, Khalil; Kim, Jaekook

    2004-01-20

    A lithium metal oxide positive electrode for a non-aqueous lithium cell is disclosed. The cell is prepared in its initial discharged state and has a general formula xLiMO.sub.2.(1-x)Li.sub.2 M'O.sub.3 in which 0

  11. Lithium metal oxide electrodes for lithium cells and batteries

    DOE Patents [OSTI]

    Thackeray, Michael M.; Johnson, Christopher S.; Amine, Khalil

    2008-12-23

    A lithium metal oxide positive electrode for a non-aqueous lithium cell is disclosed. The cell is prepared in its initial discharged state and has a general formula xLiMO.sub.2.(1-x)Li.sub.2M'O.sub.3 in which 0

  12. Manganese oxide composite electrodes for lithium batteries

    DOE Patents [OSTI]

    Johnson, Christopher S.; Kang, Sun-Ho; Thackeray, Michael M.

    2009-12-22

    An activated electrode for a non-aqueous electrochemical cell is disclosed with a precursor thereof a lithium metal oxide with the formula xLi.sub.2MnO.sub.3.(1-x)LiMn.sub.2-yM.sub.yO.sub.4 for 0.5

  13. Surface protected lithium-metal-oxide electrodes

    DOE Patents [OSTI]

    Thackeray, Michael M.; Kang, Sun-Ho

    2016-04-05

    A lithium-metal-oxide positive electrode having a layered or spinel structure for a non-aqueous lithium electrochemical cell and battery is disclosed comprising electrode particles that are protected at the surface from undesirable effects, such as electrolyte oxidation, oxygen loss or dissolution by one or more lithium-metal-polyanionic compounds, such as a lithium-metal-phosphate or a lithium-metal-silicate material that can act as a solid electrolyte at or above the operating potential of the lithium-metal-oxide electrode. The surface protection significantly enhances the surface stability, rate capability and cycling stability of the lithium-metal-oxide electrodes, particularly when charged to high potentials.

  14. Protective coating on positive lithium-metal-oxide electrodes for lithium batteries

    DOE Patents [OSTI]

    Johnson, Christopher S.; Thackeray, Michael M.; Kahaian, Arthur J.

    2006-05-23

    A positive electrode for a non-aqueous lithium cell comprising a LiMn2-xMxO4 spinel structure in which M is one or more metal cations with an atomic number less than 52, such that the average oxidation state of the manganese ions is equal to or greater than 3.5, and in which 0.ltoreq.x.ltoreq.0.15, having one or more lithium spine oxide LiM'2O4 or lithiated spinel oxide Li1+yM'2O4 compounds on the surface thereof in which M' are cobalt cations and in which 0.ltoreq.y.ltoreq.1.

  15. Anion-tunable properties and electrochemical performance of functionalized ferrocene compounds

    SciTech Connect (OSTI)

    Cosimbescu, Lelia; Wei, Xiaoliang; Vijayakumar, M.; Xu, Wu; Helm, Monte L.; Burton, Sarah D.; Sorensen, Christina M.; Liu, Jun; Sprenkle, Vincent; Wang, Wei

    2015-09-16

    We report a series of ionically modified ferrocene compounds for hybrid lithium-organic non-aqueous redox flow batteries, based on the ferrocene/ferrocenium redox couple as the active catholyte material. Tetraalkylammonium ionic moieties were incorporated into the ferrocene structure, in order to enhance the solubility of the otherwise relatively insoluble ferrocene. The effect of various counter anions of the tetraalkylammonium ionized species appended to the ferrocene, such as bis(trifluoromethanesulfonyl)imide, hexafluorophosphate, perchlorate, tetrafluoroborate, and dicyanamide on the solubility of the ferrocene was investigated. The solution chemistry of the ferrocene species was studied, in order to understand the mechanism of solubility enhancement. Finally, the electrochemical performance of these ionized ferrocene species was evaluated and shown to have excellent cell efficiency and superior cycling stability.

  16. Manganese oxide composite electrodes for lithium batteries

    DOE Patents [OSTI]

    Thackeray, Michael M. (Naperville, IL); Johnson, Christopher S. (Naperville, IL); Li, Naichao (Croton on Hudson, NY)

    2007-12-04

    An activated electrode for a non-aqueous electrochemical cell is disclosed with a precursor of a lithium metal oxide with the formula xLi.sub.2MnO.sub.3.(1-x)LiMn.sub.2-yM.sub.yO.sub.4 for 0

  17. Interface Induced Carbonate Mineralization: A Fundamental Geochemical Process Relevant to Carbon Sequestration

    SciTech Connect (OSTI)

    Teng, H. Henry; Xu, Huifang

    2013-07-17

    We have approached the long-standing geochemical question why anhydrous high-Mg carbonate minerals (i.e., magnesite and dolomite) cannot be formed at ambient conditions from a new perspective by exploring the formation of MgCO{sub 3} and Mg{sub x}Ca{sub (1-x)}CO{sub 3} in non-aqueous solutions. Data collected from our experiments in this funding period suggest that a fundamental barrier, other than cation hydration, exists that prevents Mg{sup 2+} and CO{sub 3}{sup 2-} ions from forming long-range ordered structures. We propose that this barrier mainly stems from the lattice limitation on the spatial configuration of CO{sub 3} groups in magnesite crystals. On the other hand, the measured higher distribution coefficients of Mg between magnesian calcites formed in the absence and presence of water give us a first direct proof to support and quantify the cation hydration effect.

  18. Low-temperature lithium diffusion in simulated high-level boroaluminosilicate nuclear waste glasses

    SciTech Connect (OSTI)

    Neeway, James J.; Kerisit, Sebastien N.; Gin, Stephane; Wang, Zhaoying; Zhu, Zihua; Ryan, Joseph V.

    2014-12-01

    Ion exchange is recognized as an integral, if underrepresented, mechanism influencing glass corrosion. However, due to the formation of various alteration layers in the presence of water, it is difficult to conclusively deconvolute the mechanisms of ion exchange from other processes occurring simultaneously during corrosion. In this work, an operationally inert non-aqueous solution was used as an alkali source material to isolate ion exchange and study the solid-state diffusion of lithium. Specifically, the experiments involved contacting glass coupons relevant to the immobilization of high-level nuclear waste, SON68 and CJ-6, which contained Li in natural isotope abundance, with a non-aqueous solution of 6LiCl dissolved in dimethyl sulfoxide at 90 C for various time periods. The depth profiles of major elements in the glass coupons were measured using time-of-flight secondary ion mass spectrometry (ToF-SIMS). Lithium interdiffusion coefficients, DLi, were then calculated based on the measured depth profiles. The results indicate that the penetration of 6Li is rapid in both glasses with the simplified CJ-6 glass (D6Li ? 4.0-8.0 10-21 m2/s) exhibiting faster exchange than the more complex SON68 glass (DLi ? 2.0-4.0 10-21 m2/s). Additionally, sodium ions present in the glass were observed to participate in ion exchange reactions; however, different diffusion coefficients were necessary to fit the diffusion profiles of the two alkali ions. Implications of the diffusion coefficients obtained in the absence of alteration layers to the long-term performance of nuclear waste glasses in a geological repository system are also discussed.

  19. Pore-scale flow characterization of low-interfacial tension flow through mixed-wet porous media with different pore geometries

    SciTech Connect (OSTI)

    Yadali Jamaloei, Benyamin; Asghari, Koorosh; Kharrat, Riyaz

    2011-01-15

    The low-interfacial tension flow through porous media occurs in surfactant-based enhanced oil recovery (EOR), soil clean-up, underground removal of the non-aqueous phase liquid and dense non-aqueous phase liquid, etc. In surfactant-based EOR processes, numerous works have been carried out to characterize - either qualitatively or quantitatively - the micro- and macro-scale flow behavior. What has been lacking is to link the statistics of oil blobs population (e.g., distribution of blob length and diameter) to the pore-scale phenomena and macro-scale quantities. In particular, no work has been reported to elucidate the effect of the ratio of pore body to throat diameter (i.e., aspect ratio) on the pore-scale characterization based on the blobs population statistics. The significance of the aspect ratio lies in that it describes the geometry of a porous medium and is one of the foremost morphological features. The aspect ratio is also one of the fundamental factors governing the pore-level events. This study presents the effect of aspect ratio on the statistical distribution of the blob length and equivalent diameter and links the blobs population statistics to the observed pore-level events. The pore-scale variation of the ratio of viscous-to-capillary forces acted on the oil blobs at the threshold of displacement is utilized to characterize the effect of blob length distribution at different aspect ratios. It also provides some insight into correlating the change in oil recovery efficiency and capillary number, by change in aspect ratio, with the change in blobs population statistics. (author)

  20. Technetium Sorption by Cementitious Materials Under Reducing Conditions

    SciTech Connect (OSTI)

    Kaplan, Daniel I.; Estes, Shanna L.; Powell, Brian A.

    2012-09-28

    The objective of this study was to measure technetium ({sup 99}Tc) sorption to cementitious materials under reducing conditions to simulate Saltstone Disposal Facility conditions. {sup 99}Tc(VII) batch sorption experiments were conducted for 319 days in an inert glovebag with a variety of cementitious materials (aged cement, Vault 2, TR545, and TR547) containing varying amounts of blast furnace slag. Between 154 and 319 days, the {sup 99}Tc aqueous concentrations tended to remain constant and samples amended with different initial {sup 99}Tc concentrations, tended to merge at about 10{sup -9} M for Vault 2 (17% slag) and TR545 (90% slag) and 10{sup -8} M for TR547 (45% slag). This data provided strong evidence that solubility, and not adsorption (K{sub d} values), was controlling aqueous {sup 99}Tc concentrations. Laboratory data superimposed over thermodynamic speciation diagrams further supported the conclusion that solubility, and not adsorption controlled {sup 99}Tc aqueous concentrations. The oxidation state of the aqueous {sup 99}Tc at the end of the sorption experiment was determined by solvent extraction to be almost entirely {sup 99}Tc(VII). The pH of the present system was ~11.8. Previously proposed solubility controlling phases including Tc-sulfides may be present, but do not appear to control solubility. After the 319 day sorption period, the suspensions were removed from the glovebag and a desorption step under oxic conditions was conducted for 20 days by adding oxic, pH-buffered solutions to the suspensions. {sup 99}Tc aqueous concentrations increased by more than an order of magnitude and Eh increased by several hundred millivolts within 24 hours after the introduction of the oxic solutions. These desorption results are consistent with re-oxidation and dissolution/desorption of {sup 99}Tc(IV) phases possibly present in the cementitious materials after the anoxic sorption step of the experiment. Aqueous {sup 99}Tc concentrations continued to increase

  1. Particle Physics at the University of Pittsburgh Summary Report for Proposal Period FY'09-11

    SciTech Connect (OSTI)

    Boudreau, Joe; Dytman, Steven; Mueller, James; Naples, Donna; Paolone, Vittorio; Savinov, Vladimir

    2012-10-01

    Presented is the final summary report for grant DOE-FG02-91ER40646. The HEP group at the University consists of three tasks: B,D and L. Task B supports Pitt's CDF group at the energy frontier which includes Joe Boudreau and Paul Shepard. Work of the group includes Hao Song's thesis on the measurement of the B_c lifetime using exclusive J/psi+pion decays, and an update of the previous B_c semi-leptonic analyses under the supervision of Paul Shepard. Task D supports Pitt's neutrino group at the intensity frontier which includes PIs Dytman, Naples and Paolone. The group also includes postdoctoral research associate Danko, and thesis students Isvan (MINOS), Eberly (Minerva ), Ren (Minerva )and Hansen (T2K). This report summarizes their progress on ongoing experiments which are designed to make significant contributions to a detailed understanding of the neutrino mixing matrix. Task L supports Pitt's ATLAS group at the energy frontier and includes investigators Vladimir Savinov, James Mueller and Joe Boudreau. This group contributed both to hardware (calorimeter electronics, Savinov) and to software (Simulation, Detector Description, and Visualization: Boudreau and Mueller; MC generators: Savinov) and a summary of their progress is presented.

  2. Sorption of colloids, organics, and metals onto gas-water interfaces: Transport mechanisms and potential remediation technology. 1998 annual progress report

    SciTech Connect (OSTI)

    Wan, J.; Tokunaga, T.K.

    1998-06-01

    'Although contaminant sorption at mineral surfaces has received much recognition as a major mechanism controlling contaminant behavior in subsurface environments, virtually no attention has been given to the possibility of contaminant sorption at gas-water interfaces. Moreover, no effort has yet been advanced to optimize such interactions for the purpose of facilitating in-situ remediation. Gas-water interfaces, unlike water-solid interfaces, are mobile. Therefore, associations of contaminants with gas-water interfaces can be very important not only in subsurface contaminant distributions, but also in contaminant transport, and potentially in remediation. The first objective of this research is to develop a quantitative understanding of interactions between contaminants and gas-water interfaces. The anticipated results will provide insights into the poorly understood phenomenon of contaminant interactions with the gas-water interface, and improve the current conceptual models of contaminant behavior in subsurface environments. The second purpose of this research is to explore the possibility of using surfactant stabilized microbubbles for in-situ remediation. Both pump-and-treat, and air sparging remediation methods are ineffective at displacing contaminants in zones which are advectively inaccessible. Stable microbubbles can migrate beyond preferential flow pathways and enter lower permeability zones by buoyant rise. The microbubbles can deliver oxygen and nutrients for promoting aerobic degradation of organic contaminants, and also deliver surfactants for emulsifying NAPLs.'

  3. P-SV conversions at a shallow boundary beneath Campi Flegrei caldera (Italy) - evidence for the magma chamber

    SciTech Connect (OSTI)

    Ferrucci, F.; Hirn, A.; De Natale, G.; Virieux, J.; Mirabile, L. Inst. de Physique du Globe, Paris Osservatorio Vesuviano, Naples CNRS, Inst. de Geodynamique, Valbonne Ist. Universitario Navale, Naples )

    1992-10-01

    Seismograms from an active seismic experiment carried out at Campi Flegrei caldera (near Naples, Italy), show a large-amplitude SV-polarized shear wave, following by less than 1.5-s P waves reflected at wide angle from a deep crustal interface. Early arriving SV-polarized waves, with the same delay to direct P waves, are also observed in seismograms from a regional 280 km-deep, magnitude 5.1 earthquake. Such short delays of S to P waves are consistent with a P-SV conversion on transmission occurring at a shallow boundary beneath the receivers. The large amplitude of the converted-SV phase, along with that the P waves are near vertical, requires a boundary separating a very low rigidity layer from the upper caldera fill. The converted phases are interpreted as a seismic marker of a magma chamber. The top of this magma chamber is located slightly deeper than the deepest earthquakes observed during the 1982-1984 unrest of Campi Flegrei. 8 refs.

  4. Ther FERMI FEL project at TRIESTE

    SciTech Connect (OSTI)

    Walker, R.P.; Bulfone, D.; Cargnello, F.

    1995-12-31

    The goal of the FERMI project - Free Electron Radiation and Matching Instrumentation - is to construct a new user facility for FEL radiation beams covering a broad spectral range (2-250 {mu}m) to complement the high brightness VUV/Soft-Xray radiation available from the ELETTRA synchrotron radiation facility at Trieste. A unique feature of the project will be the possibility of carrying out {open_quote}pump-probe{close_quote} experiments using synchronized radiation beams from FERMI and ELETTRA on the same sample. The project was launched at a meeting with Italian FEL experts held in Trieste on the 18th November 1994, chaired by C. Rubbia, as a collaboration between Sincrotrone Trieste, ENEA (Frascati), INFN (Frascati) and the University of Naples (Department of Electronic Engineering). The facility will make use of an existing linac, that forms part of the ELETTRA injection system, and a hall into which the beam can be extracted. In addition, for the first phase of the project equipment will be used from the suspended INFN/ENEA {open_quote}SURF{close_quote} FEL experiment, including the undulator, beam transport magnets and optical cavity. In this first International FEL Conference report on the project, we summarize the main features of the project, concentrating in particular on the most recent activities, including: results of measurements of the linac beam in the FEL mode of operation, further studies of the electron beam transport system including possibilities for bunch length manipulations, and further numerical calculations of the FEL performance.

  5. Cost-benefit analysis of cosolvent flushing to treat groundwater contamination source areas

    SciTech Connect (OSTI)

    Anason, S.L.

    1999-03-01

    Dense non-aqueous phase liquids (DNAPLs) in the zone beneath the water table can be a virtually permanent source of groundwater contamination that cannot be remediated by currently available technologies. Cosolvent flushing is a new technology that has the potential to remediate these sites and could pose a solution to the problem of DNAPL source areas. A computer model was developed to determine the cost and time to remediate an aquifer using cosolvent flushing. Included in the model is a module to calculate the costs of recycling the alcohol that is used as the cosolvent. The model was validated using site conditions to a prior study. It was determined that recycling the cosolvent allows cosolvent flushing to be a cost effective alternative to surfactant flushing, another new technology being considered for DNAPL source remediation. Sensitivity analysis of the model was conducted by varying the saturation percentage of contaminant, percentage and type of alcohol used in the cosolvent mixture, site hydraulic conductivity, and the contaminant. Five alcohols were modeled: methanol, ethanol, 1-isopropanol, 2-isopropanol, and tert-butyl-alcohol (TBA). 1-Isopropanol, 2-isopropanol, and TBA were always more expensive than methanol and ethanol.

  6. Passive recovery of DNAPL from clayey soil via vertical collection wells

    SciTech Connect (OSTI)

    Tease, B.; Gagnon, D.

    1995-12-01

    A release of dense non-aqueous phase liquids (DNAPL) from two underground storage tanks (USTs), created a contaminant plume that extended approximately 30 feet into lacustrine sediments comprised mainly of varved clay. Subsurfaces investigations indicated that the release was comprised primarily of the chlorinated solvent Trichloroethene which had migrated horizontally approximately 250 feet cross-gradient to groundwater flow. A relatively narrow zone of free phase product extended from the UST area approximately 150-200 feet along the plume of migration at a depth of 20-30 feet below the ground surface. Since clay varves interconnected by vertical fractures is believed to have facilitated the DNAPL migration, 4{close_quotes} diameter stainless steel collection recovery of 10-20 quarts of DNAPL per each collection event, over a 4 month period supported what is believed to be preferential DNAPL migration. DNAPL recovery continued for a total of 6 months before the point of diminimus return (1-2 quarts/month) resulted in adopting a quarterly recovery schedule. To date, 201 quarts of free phase DNAPL have been recovered. DNAPL mobility, delineation, well installation and collection techniques are discussed. Compared to conventional remediation alternatives, this passive recovery system provides an innovative approach to a difficult and costly problem; recovery of DNAPL isolated within clay.

  7. Long-term proliferation and safeguards issues in future technologies

    SciTech Connect (OSTI)

    Keisch, B.; Auerbach, C.; Fainberg, A.; Fiarman, S.; Fishbone, L.G.; Higinbotham, W.A.; Lemley, J.R.; O'Brien, J.

    1986-02-01

    The purpose of the task was to assess the effect of potential new technologies, nuclear and non-nuclear, on safeguards needs and non-proliferation policies, and to explore possible solutions to some of the problems envisaged. Eight subdivisions were considered: New Enrichment Technologies; Non-Aqueous Reprocessing Technologies; Fusion; Accelerator-Driven Reactor Systems; New Reactor Types; Heavy Water and Deuterium; Long-Term Storage of Spent Fuel; and Other Future Technologies (Non-Nuclear). For each of these subdivisions, a careful review of the current world-wide effort in the field provided a means of subjectively estimating the viability and qualitative probability of fruition of promising technologies. Technologies for which safeguards and non-proliferation requirements have been thoroughly considered by others were not restudied here (e.g., the Fast Breeder Reactor). The time scale considered was 5 to 40 years for possible initial demonstration although, in some cases, a somewhat optimistic viewpoint was embraced. Conventional nuclear-material safeguards are only part of the overall non-proliferation regime. Other aspects are international agreements, export controls on sensitive technologies, classification of information, intelligence gathering, and diplomatic initiatives. The focus here is on safeguards, export controls, and classification.

  8. Hybrid joule heating/electro-osmosis process for extracting contaminants from soil layers

    DOE Patents [OSTI]

    Carrigan, Charles R.; Nitao, John J.

    2003-06-10

    Joule (ohmic) heating and electro-osmosis are combined in a hybrid process for removal of both water-soluble contaminants and non-aqueous phase liquids from contaminated, low-permeability soil formations that are saturated. Central to this hybrid process is the partial desaturation of the formation or layer using electro-osmosis to remove a portion of the pore fluids by induction of a ground water flow to extraction wells. Joule heating is then performed on a partially desaturated formation. The joule heating and electro-osmosis operations can be carried out simultaneously or sequentially if the desaturation by electro-osmosis occurs initially. Joule heating of the desaturated formation results in a very effective transfer or partitioning of liquid state contaminants to the vapor phase. The heating also substantially increases the vapor phase pressure in the porous formation. As a result, the contaminant laden vapor phase is forced out into soil layers of a higher permeability where other conventional removal processes, such as steam stripping or ground water extraction can be used to capture the contaminants. This hybrid process is more energy efficient than joule heating or steam stripping for cleaning low permeability formations and can share electrodes to minimize facility costs.

  9. Electric current-producing device having sulfone-based electrolyte

    DOE Patents [OSTI]

    Angell, Charles Austen; Sun, Xiao-Guang

    2010-11-16

    Electrolytic solvents and applications of such solvents including electric current-producing devices. For example, a solvent can include a sulfone compound of R1--SO2--R2, with R1 being an alkyl group and R2 a partially oxygenated alkyl group, to exhibit high chemical and thermal stability and high oxidation resistance. For another example, a battery can include, between an anode and a cathode, an electrolyte which includes ionic electrolyte salts and a non-aqueous electrolyte solvent which includes a non-symmetrical, non-cyclic sulfone. The sulfone has a formula of R1--SO2--R2, wherein R1 is a linear or branched alkyl or partially or fully fluorinated linear or branched alkyl group having 1 to 7 carbon atoms, and R2 is a linear or branched or partially or fully fluorinated linear or branched oxygen containing alkyl group having 1 to 7 carbon atoms. The electrolyte can include an electrolyte co-solvent and an electrolyte additive for protective layer formation.

  10. Removal of Mercury from Aqueous Streams of Fossil Fuel Power Plants Using Novel Functionalized Nanoporous Sorbents

    SciTech Connect (OSTI)

    Mattigod, Shas V.; Fryxell, Glen E.; Feng, X; Parker, Kent E.; Pierce, Eric M.

    2006-01-11

    A new class of hybrid nanoporous materials has been developed at the Pacific Northwest National Laboratory for removing toxic heavy metals such as mercury from aqueous and nonaqueous waste streams. These novel materials consist of functional molecules capable of selectively binding mercury (thiol groups) covalently bound (as densely populated monolayers) to the synthetic nanoporous substrates. Tests indicated that this sorbent (Self-Assembled Monolayers on Mesoporous Silica - SAMMS) can achieve mercury loading as high as {approx}635 mg/g. The high affinity for Hg adsorption by this material was reflected by Kd values as high as 3.5 x 108 ml/g. Data indicated that SAMMS can adsorb both inorganic and organic forms of mercury. Experimental data indicated that mercury adsorption performance of SAMMS was not significantly affected by pH, ionic strength, presence of other cations (Na, Ca, Cd, Cu, Fe, Ni, Pb, and Zn), and complexing anions (Cl, CN, CO3, SO4, and PO4) in solution. Adsorption kinetics studies indicated that SAMMS adsorbed mercury very rapidly (about 99.9% adsorption occurring within first five minutes). Tests conducted using samples of different aqueous and non-aqueous waste streams have confirmed the exemplary performance characteristics of SAMMS sorbents. Preliminary cost estimates indicated that using SAMMS would result in significant savings in mercury remediation costs as compared to the use of conventional adsorbents such as ion exchange resin and activated carbon.