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Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


1

Yucca Mountain Area Saturated Zone Dissolved Organic Carbon Isotopic Data  

SciTech Connect (OSTI)

Groundwater samples in the Yucca Mountain area were collected for chemical and isotopic analyses and measurements of water temperature, pH, specific conductivity, and alkalinity were obtained at the well or spring at the time of sampling. For this project, groundwater samples were analyzed for major-ion chemistry, deuterium, oxygen-18, and carbon isotopes of dissolved inorganic carbon (DIC) and dissolved organic carbon (DOC). The U.S. Geological Survey (USGS) performed all the fieldwork on this project including measurement of water chemistry field parameters and sample collection. The major ions dissolved in the groundwater, deuterium, oxygen-18, and carbon isotopes of dissolved inorganic carbon (DIC) were analyzed by the USGS. All preparation and processing of samples for DOC carbon isotopic analyses and geochemical modeling were performed by the Desert Research Institute (DRI). Analysis of the DOC carbon dioxide gas produced at DRI to obtain carbon-13 and carbon-14 values was conducted at the University of Arizona Accelerator Facility (a NSHE Yucca Mountain project QA qualified contract facility). The major-ion chemistry, deuterium, oxygen-18, and carbon isotopes of DIC were used in geochemical modeling (NETPATH) to determine groundwater sources, flow paths, mixing, and ages. The carbon isotopes of DOC were used to calculate groundwater ages that are independent of DIC model corrected carbon-14 ages. The DIC model corrected carbon-14 calculated ages were used to evaluate groundwater travel times for mixtures of water including water beneath Yucca Mountain. When possible, groundwater travel times were calculated for groundwater flow from beneath Yucca Mountain to down gradient sample sites. DOC carbon-14 groundwater ages were also calculated for groundwaters in the Yucca Mountain area. When possible, groundwater travel times were estimated for groundwater flow from beneath Yucca Mountain to down gradient groundwater sample sites using the DOC calculated groundwater ages. The DIC calculated groundwater ages were compared with DOC calculated groundwater ages and both of these ages were compared to travel times developed in ground-water flow and transport models. If nuclear waste is stored in Yucca Mountain, the saturated zone is the final barrier against the release of radionuclides to the environment. The most recent rendition of the TSPA takes little credit for the presence of the saturated zone and is a testament to the inadequate understanding of this important barrier. If radionuclides reach the saturated zone beneath Yucca Mountain, then there is a travel time before they would leave the Yucca Mountain area and flow down gradient to the Amargosa Valley area. Knowing how long it takes groundwater in the saturated zone to flow from beneath Yucca Mountain to down gradient areas is critical information for potential radionuclide transport. Radionuclide transport in groundwater may be the quickest pathway for radionuclides in the proposed Yucca Mountain repository to reach land surface by way of groundwater pumped in Amargosa Valley. An alternative approach to ground-water flow and transport models to determine the travel time of radionuclides from beneath Yucca Mountain to down gradient areas in the saturated zone is by carbon-14 dating of both inorganic and organic carbon dissolved in the groundwater. A standard method of determining ground-water ages is to measure the carbon-13 and carbon-14 of DIC in the groundwater and then correct the measured carbon-14 along a flow path for geochemical reactions that involve carbon containing phases. These geochemical reactions are constrained by carbon-13 and isotopic fractionations. Without correcting for geochemical reactions, the ground-water ages calculated from only the differences in carbon-14 measured along a flow path (assuming the decrease in carbon-14 is due strictly to radioactive decay) could be tens of thousands of years too old. The computer program NETPATH, developed by the USGS, is the best geochemical program for correcting carbon-14 activities for geochemical r

Thomas, James; Decker, David; Patterson, Gary; Peterman, Zell; Mihevc, Todd; Larsen, Jessica; Hershey, Ronald

2007-06-25T23:59:59.000Z

2

The distribution of dissolved and particulate organic carbon in the southeastern Indian Ocean  

E-Print Network [OSTI]

. rbe rloSxee of NASTI. R OP SCIENCE Decerabex 1976 Na)or Subject: OueanoStaPby THE DISTRIBUTION OF DISSOLVED AND PARTICULATE ORGANIC CARBON IN THE SOUTHEASTERN INDIAN OCEAN A Thesis by HUSSEIN ANWAR ABD EL-REHEIM (Co-Chairman of ommittee) (Co...-C irman of Commit e) (Head of Department) (Member) r (Member) December 1976 ABSTtlACT The Distribution of Dissolved and Particulate Organic Carbon In the Southeastern Indian Ocean. (December 1976) Hussein Anwan Abd El-Reheim B. Sc. , Alexandria...

Abd El-Reheim, Hussein Anwar

1976-01-01T23:59:59.000Z

3

Determining Sources of Dissolved Organic Carbon and Nutrients in an Urban Basin Using Novel and Traditional Methods  

E-Print Network [OSTI]

Water quality in urban ecosystems is sensitive to localized disturbances potentially affecting those mechanisms which influence nutrient cycles. The Carters Creek Basin has been reported to have elevated concentrations of dissolved organic carbon...

Govil, Krittika

2014-01-03T23:59:59.000Z

4

Dissolved organic carbon dynamics in anaerobic sediments of the Santa Monica Basin  

E-Print Network [OSTI]

an organic-rich coastal sediment. Geochim. Cosmochim. Actaorganic carbon in sediments from the North Carolinaexchange between deep ocean sediments and sea water. Nature

2013-01-01T23:59:59.000Z

5

A method for the determination of dissolved organic carbon in sea water by gas chromatography  

E-Print Network [OSTI]

of organic matter was carried out at elevated temperature and pressure after collection of a large number of samples. The resulting carbon dioxide was flushed through a gas chromatograph with helium as the carrier gas and the signal was recorded on a strip... chart recorder. Chromatographic analysis time was approximately eleven minutes per sample with a precision of + Q. 1 mg C/l. The organic carbon content of the sample was determined by measurement of the peak area using an appropriate carbon dioxide...

Fredericks, Alan D

1965-01-01T23:59:59.000Z

6

Study of dissolved organic matter in peatlands: molecular characterisation of a dynamic carbon reservoir   

E-Print Network [OSTI]

Northern peatlands represent a significant carbon reservoir, containing approximately a third of the terrestrial carbon pool. The stability of these carbon stores is poorly understood, and processes of accumulation and ...

Ridley, Luke McDonald

2014-06-30T23:59:59.000Z

7

Dissolved organic matter properties and their relationship to carbon dioxide efflux from  

E-Print Network [OSTI]

of Bayreuth, 95440 Bayreuth, Germany c Department of Geography and Centre for Climate and Global Change 2001; accepted 9 December 2002 Abstract The effects of peat bog harvesting and restoration on dissolved- centrations, humification indices derived from synchronous fluorescence spectra (humification index (HIX

Moore, Tim

8

Fractionation of Dissolved Solutes and Chromophoric Dissolved Organic Matter During Experimental Sea Ice Formation.  

E-Print Network [OSTI]

In the past decade there has been an overall decrease in Arctic Ocean sea ice cover. Changes to the ice cover have important consequences for organic carbon cycling, especially over the continental shelves. When sea ice is formed, dissolved organic...

Smith, Stephanie 1990-

2012-04-16T23:59:59.000Z

9

The effect of water temperature on the adsorption equilibrium of dissolved organic matter and atrazine on granular activated carbon  

SciTech Connect (OSTI)

The influence of water temperature on the adsorption of natural dissolved organic matter (DOM) on activated carbon has not been investigated intensively yet. In this study, batch experiments with granular activated carbon (GAC) F300, from bituminous coal, have been carried out at three temperatures (5, 20, 35{sup o} C) using a humic acid model water and different types of surface water (lake, river, canal). Furthermore, the adsorption of an anthropogenic contaminant, atrazine, was quantified in the absence and presence of DOM. The results indicate a significant influence of water temperature on the adsorption equilibrium of DOM and atrazine. Contrary to expectations, DOM and atrazine adsorption in surface water tends to be increased with increasing water temperature, whereas the extent of this effect is dependent on the type and concentration of DOM. Furthermore, the temperature effect on atrazine adsorption is controlled by competition of DOM and atrazine on adsorption sites. Some assumptions are proposed and discussed for explaining the temperature effects observed in the batch studies. 39 refs., 4 figs., 2 tabs.

Bernd Schreiber; Viktor Schmalz; Thomas Brinkmann; Eckhard Worch [Dresden University of Technology, Dresden (Germany). Institute of Water Chemistry

2007-09-15T23:59:59.000Z

10

APPLICATION OF CARBOHYDRATES AND PHENOLS AS BIOMARKERS TO STUDY DISSOLVED ORGANIC MATTER RESERVOIRS IN ARCTIC RIVERS.  

E-Print Network [OSTI]

Arctic rivers are the dominant pathways for the transport of terrestrial dissolved organic carbon to the Arctic Ocean, but knowledge of sources, transformations and transfer of organic carbon and nitrogen in Arctic river watersheds is extremely...

McMahon, Rachel

2014-01-22T23:59:59.000Z

11

PII S0016-7037(99)00066-6 Fluxes of dissolved organic carbon from California continental margin sediments  

E-Print Network [OSTI]

sediments DAVID J. BURDIGE,1, * WILLIAM M. BERELSON,2 KENNETH H. COALE,3 JAMES MCMANUS,4 and KENNETH S) from marine sediments represent a poorly constrained component of the oceanic carbon cycle that may measurements of DOC fluxes from continental margin sediments (water depths ranging from 95 to 3,700 m

Burdige, David

12

Total Organic Carbon Analyzer | EMSL  

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

Total Organic Carbon Analyzer Total Organic Carbon Analyzer The carbon analyzer is used to analyze total carbon (TC), inorganic carbon (IC), total organic carbon (TOC), purgeable...

13

Microbial community transcriptomes reveal microbes and metabolic pathways associated with dissolved organic matter turnover in the sea  

E-Print Network [OSTI]

Marine dissolved organic matter (DOM) contains as much carbon as the Earth's atmosphere, and represents a critical component of the global carbon cycle. To better define microbial processes and activities associated with ...

McCarren, Jay

14

Dissolved organic matter in Chesapeake Bay sediment pore waters  

E-Print Network [OSTI]

Dissolved organic matter in Chesapeake Bay sediment pore waters David J. Burdige * Department of recent studies of dissolved organic matter (DOM) in Chesapeake Bay sediment pore waters are summar- ized water DOM. This analysis shows that much of the DOM accumulating in sediment pore waters appears

Burdige, David

15

Microbial production and consumption of marine dissolved organic matter  

E-Print Network [OSTI]

Marine phytoplankton are the principal producers of oceanic dissolved organic matter (DOM), the organic substrate responsible for secondary production by heterotrophic microbes in the sea. Despite the importance of DOM in ...

Becker, Jamie William

2013-01-01T23:59:59.000Z

16

PHOTOINDUCTIVE DEGRADATION OF TWO ESTROGENS BY NATURAL DISSOLVED ORGANIC  

E-Print Network [OSTI]

PHOTOINDUCTIVE DEGRADATION OF TWO ESTROGENS BY NATURAL DISSOLVED ORGANIC MATTER UNDER SIMULATED on the nature and origin of the media (Thurman 1985) Photodegradation - degradation (break of aromatic HPLC-UV Spectrophotometer, Fluorimeter, TOCmeter Suntest 8h, 250 W/m2, 900 kJ/h : - ~ 800 nM E1 or E2

Boyer, Edmond

17

Rapid extraction of dissolved inorganic carbon from seawater and groundwater samples for radiocarbon dating  

E-Print Network [OSTI]

The focus of this thesis is the design and development of a system for rapid extraction of dissolved inorganic carbon from seawater and groundwater samples for radiocarbon dating. The Rapid Extraction of Dissolved Inorganic ...

Gospodinova, Kalina Doneva

2012-01-01T23:59:59.000Z

18

Photolytic processing of secondary organic aerosols dissolved in cloud droplets  

SciTech Connect (OSTI)

The effect of UV irradiation on the molecular composition of aqueous extracts of secondary organic aerosol (SOA) was investigated. SOA was prepared by the dark reaction of ozone and d-limonene at 0.05 - 1 ppm precursor concentrations and collected with a particle-into-liquid sampler (PILS). The PILS extracts were photolyzed by 300 - 400 nm radiation for up to 24 hours. Water-soluble SOA constituents were analyzed using high-resolution electrospray ionization mass spectrometry (HR-ESI-MS) at different stages of photolysis for all SOA precursor concentrations. Exposure to UV radiation increased the average O/C ratio and decreased the average double bond equivalent (DBE) of the dissolved SOA compounds. Oligomeric compounds were significantly reduced by photolysis relative to the monomeric compounds. Direct pH measurements showed that compounds containing carboxylic acids increased upon photolysis. Methanol reactivity analysis revealed significant photodissociation of molecules containing carbonyl groups and formation of carboxylic acids. Aldehydes, such as limononaldehyde, were almost completely removed. The removal of carbonylswas confirmed by the UV-Vis absorption spectroscopy of the SOA extracts where the absorbance in the carbonyl n??* band decreased significantly upon photolysis. The effective quantum yield (the number of carbonyls destroyed per photon absorbed) was estimated as ~ 0.03. The concentration of peroxides did not change significantly during photolysis as quantified with an iodometric test. Although organic peroxides were photolyzed, the likely end products of photolysis were smaller peroxides, including hydrogen peroxide, resulting in a no net change in the peroxide content.

Bateman, Adam P.; Nizkorodov, Serguei; Laskin, Julia; Laskin, Alexander

2011-05-26T23:59:59.000Z

19

Aged black carbon identified in marine dissolved organic carbon  

E-Print Network [OSTI]

pool in the northeast Pacific Ocean, Deep Sea Res. , Part I,?445‰ in the deep NE Pacific Ocean (Table S1). The Suwanneein the northeast Pacific Ocean. If the BC in the Amazon

Ziolkowski, Lori A; Druffel, Ellen R.M.

2010-01-01T23:59:59.000Z

20

Chemical characterization of dissolved organic matter (DOM) in seawater : structure, cycling, and the role of biology  

E-Print Network [OSTI]

The goal of this thesis is to investigate three different areas relating to the characterization of dissolved organic matter (DOM): further determination of the chemical compounds present in high molecular weight DOM ...

Quan, Tracy M. (Tracy Michelle), 1977-

2005-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


21

Direct and indirect photoreactions of chromophoric dissolved organic matter : roles of reactive oxygen species and iron  

E-Print Network [OSTI]

Photochemical transformations of chromophoric dissolved organic matter (CDOM) are one of the principal processes controlling its fate in coastal waters. The photochemical decomposition of CDOM leads to the formation of a ...

Goldstone, Jared Verrill, 1971-

2002-01-01T23:59:59.000Z

22

Photochemical and microbial degradation of dissolved lignin phenols: Implications for the fate of terrigenous dissolved organic matter in  

E-Print Network [OSTI]

Photochemical and microbial degradation of dissolved lignin phenols: Implications for the fate level characterizations of dissolved lignin were conducted in Mississippi River plume waters to study degradation were the primary factors affecting lignin concentrations. At salinities >25 psu, photooxidation

Hernes, Peter J.

23

Biogeochemical and hydrographic controls on chromophoric dissolved organic matter distribution in the Pacific Ocean  

E-Print Network [OSTI]

in the Pacific Ocean Chantal M. Swan a,Ă?, David A. Siegel a,b , Norman B. Nelson a , Craig A. Carlson c , Elora Available online 19 September 2009 Keywords: CDOM AOU Pacific Water masses Hydrography Bio-optical a b s t r a c t Recent in situ observations of chromophoric dissolved organic material (CDOM) in the Pacific

Siegel, David A.

24

Supplemental Data Insights into Dissolved Organic Matter Complexity in Rainwater from Continental  

E-Print Network [OSTI]

Supplemental Data Insights into Dissolved Organic Matter Complexity in Rainwater from. Storm Number Storm Type Date Collected Amount (mm) pH DOC (µM) 688 Terrestrial 3/17/07 8.6 4.7 64.6 718

Meskhidze, Nicholas

25

Occurrence and Implication of dissolved organic phosphorus (DOP) in tertiary wastewater Effluents Page 1 of 6  

E-Print Network [OSTI]

GU, APRIL Occurrence and Implication of dissolved organic phosphorus (DOP) in tertiary wastewater wastewater effluents L. Liu1 , D. S. Smith2 , M. Bracken3 , J.B. Neethling4 , H.D. Stensel5 and S. Murthy6 levels (e.g. TPwastewater treatment plants. A few previous studies (Benisch et al., 2007

Brody, James P.

26

5, 11391174, 2008 Organic carbon and  

E-Print Network [OSTI]

BGD 5, 1139­1174, 2008 Organic carbon and nutrient export from disturbed peatlands S. Waldron et al of Biogeosciences The significance of organic carbon and nutrient export from peatland-dominated landscapes subject Union. 1139 #12;BGD 5, 1139­1174, 2008 Organic carbon and nutrient export from disturbed peatlands S

Boyer, Edmond

27

Predicting the oceanic input of organic carbon by continental erosion  

SciTech Connect (OSTI)

Empirical models were developed to describe relationships between the climatic, biologic, and geomorphologic characteristics of major world rivers and the observed dissolved and particulate carbon fluxes. The main purpose of the study was to determine the best regression models to describe river carbon flux at a global scale. Model parameters were grouped in all possible combinations and in a way to minimize the effects of multicollinearity. All parameter combinations were then tested individually. A model was developed with parameters which corresponded well to field results and global carbon fluxes which were close to previous estimates. The model was also used to relate the variability of annual carbon fluxes to the environmental variability of river basins. The statistical approach allows only a general view, but is capable of identifying the principal factors controlling global organic carbon flux. 111 refs., 5 figs., 4 tabs.

Ludwig, W.; Probst, J.C. [Centre National de la Recherche Scientifique, Strasbourg (France)] [Centre National de la Recherche Scientifique, Strasbourg (France); Kempe, S. [Technische Hochschule Darmstadt (Germany)] [Technische Hochschule Darmstadt (Germany)

1996-03-01T23:59:59.000Z

28

PAPER www.rsc.org/pps | Photochemical & Photobiological Sciences Alteration of chromophoric dissolved organic matter by solar UV radiation  

E-Print Network [OSTI]

the lagoon that were incubated in the pre-exposed water for 5 h in the dark. Cell abundance, activity dissolved organic matter by solar UV radiation causes rapid changes in bacterial community composition We evaluated the effect of photochemical alterations of chromophoric dissolved organic matter (CDOM

Sommaruga, Ruben

29

Carbon Allocation in Underground Storage Organs  

E-Print Network [OSTI]

Carbon Allocation in Underground Storage Organs Studies on Accumulation of Starch, Sugars and Oil Cover: Starch granules in cells of fresh potato tuber visualised by iodine staining. #12;Carbon By increasing knowledge of carbon allocation in underground storage organs and using the knowledge to improve

30

Subsurface Monitor for Dissolved Inorganic Carbon at Geological Sequestration Site Phase 1 SBIR Final Report  

SciTech Connect (OSTI)

Phase I research of this SBIR contract has yielded anticipated results and enable us to develop a practical new instrument to measure the Dissolved Inorganic Carbons (DIC) as well as Supercritical (SC) CO2 in underground brine water at higher sensitivity, lower cost, higher frequency and longer period of time for the Monitoring, Verification & Accounting (MVA) of CO2 sequestration as well as Enhanced Oil Recovery (EOR). We show that reduced cost and improved performance are possible; both future and emerging market exist for the proposed new instrument.

Sheng Wu

2012-08-03T23:59:59.000Z

31

STUDIES ON THE USE OF CARBON DIOXIDE DISSOLVED IN REFRIGERATED BRINE FOR THE PRESERVATION OF WHOLE FISH  

E-Print Network [OSTI]

of water by species of low oil content, such as sole and cod, and an increase in total salt. Con- trolling, NO. Z, 1971. Use of carbon dioxide gas dissolved in re- frigerated seawater seemed promising as an in experiments on holding fish in tanks, carbon dioxide decreased the rate at which their quality was degraded

32

Corrosion Testing of Carbon Steel in Oxalic Acid that Contains Dissolved Iron  

SciTech Connect (OSTI)

Radioactive liquid waste has been stored in underground carbon steel tanks for nearly 60 years at the Savannah River Site. The site is currently in the process of removing the waste from these tanks in order to place it into vitrified, stable state for longer term storage. The last stage in the removal sequence is a chemical cleaning step that breaks up and dissolves metal oxide solids that cannot be easily pumped out of the tank. Oxalic acid (OA) will be used to chemically clean the tanks after waste retrieval is completed. The waste tanks at SRS were constructed from carbon steel materials and thus are vulnerable to corrosion in acidic media. In addition to structural impacts, the impact of corrosion on the hydrogen generated during the process must be assessed. Electrochemical and coupon immersion tests were used to investigate the corrosion mechanism at anticipated process conditions. The testing showed that the corrosion rates were dependent upon the reduction of the iron species that had dissolved in solution. Initial corrosion rates were elevated due to the reduction of the ferric species to ferrous species. At later times, as the ferric species depleted, the corrosion rate decreased. On the other hand, the hydrogen evolution reaction became more dominant.

Wiersma, Bruce J.; Mickalonis, John I.; Subramanian, Karthik H.

2012-10-11T23:59:59.000Z

33

Organizing Carbon Nanotubes with Liquid Crystals  

E-Print Network [OSTI]

Organizing Carbon Nanotubes with Liquid Crystals Michael D. Lynch and David L. Patrick* Department, 2002; Revised Manuscript Received September 13, 2002 ABSTRACT Single- and multiwalled carbon nanotubes- and multiwalled carbon nanotubes (SWCNT and MWCNT) are of particular interest because these materials

Patrick, David L.

34

Worldwide organic soil carbon and nitrogen data  

SciTech Connect (OSTI)

The objective of the research presented in this package was to identify data that could be used to estimate the size of the soil organic carbon pool under relatively undisturbed soil conditions. A subset of the data can be used to estimate amounts of soil carbon storage at equilibrium with natural soil-forming factors. The magnitude of soil properties so defined is a resulting nonequilibrium values for carbon storage. Variation in these values is due to differences in local and geographic soil-forming factors. Therefore, information is included on location, soil nitrogen content, climate, and vegetation along with carbon density and variation.

Zinke, P.J.; Stangenberger, A.G. [Univ. of California, Berkeley, CA (United States). Dept. of Forestry and Resource Management; Post, W.M.; Emanual, W.R.; Olson, J.S. [Oak Ridge National Lab., TN (United States)

1986-09-01T23:59:59.000Z

35

Metal binding to dissolved organic matter and adsorption to ferrihydrite in shallow peat groundwaters: Application to diamond exploration  

E-Print Network [OSTI]

Metal binding to dissolved organic matter and adsorption to ferrihydrite in shallow peat t The speciation and solubility of kimberlite pathfinder metals (Ni, Nd, Ba and K) in shallow peat ground- waters with kimberlite pathfinder metals and determine the spatial distribution of those metals in shallow peat

36

Effects of Organic Carbon Supply Rates on Uranium Mobility in a  

E-Print Network [OSTI]

respiration caused increased (bi)carbonate concentration and formation of stable uranyl carbonate complexes remediation. Dissolved oxygen, nitrate and denitrification products have been demonstrated to mobilize U

Hazen, Terry

37

A study of the remineralization of organic carbon in nearshore sediments using carbon isotopes  

E-Print Network [OSTI]

A study of the remineralization of organic carbon was conducted in the organic-rich sediments of Buzzards Bay, MA. Major processes affecting the carbon chemistry in sediments are reflected by changes in the stable carbon ...

McNichol, Ann P., 1956-

1986-01-01T23:59:59.000Z

38

The Relationships of Particulate Matter and Particulate Organic Carbon with Hypoxic Conditions Along the Texas-Louisiana Shelf  

E-Print Network [OSTI]

an onboard surface-water flow-through system, CTD casts, and by an undulating towed vehicle. Total particulate matter and particulate organic carbon samples were obtained from Niskin bottles on CTD casts. Samples were also taken to measure dissolved oxygen...

Zuck, Nicole A

2014-08-06T23:59:59.000Z

39

The Stability of Organic Solvents and Carbon Electrode in Nonaqueous...  

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

The Stability of Organic Solvents and Carbon Electrode in Nonaqueous Li-O2 Batteries. The Stability of Organic Solvents and Carbon Electrode in Nonaqueous Li-O2 Batteries....

40

Dissolved inorganic carbon isotopic composition of low-temperature axial and ridge-flank hydrothermal fluids of the Juan de Fuca Ridge  

E-Print Network [OSTI]

carbon isotopic composition of low-temperature axial and ridge-flank hydrothermal fluids of the Juan deDissolved inorganic carbon isotopic composition of low-temperature axial and ridge-flank hydrothermal fluids of the Juan de Fuca Ridge Brett D. Walker a,, Matthew D. McCarthy a , Andrew T. Fisher b

Fisher, Andrew

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


41

Assessment of terrigenous organic carbon input to the total organic carbon in sediments from Scottish transitional waters Hydrology and Earth System Sciences, 6(6), 959970 (2002) EGS  

E-Print Network [OSTI]

Assessment of terrigenous organic carbon input to the total organic carbon in sediments from of terrigenous organic carbon input to the total organic carbon in sediments from Scottish transitional waters This paper addresses the assessment of terrestrially derived organic carbon in sediments from two Scottish

Paris-Sud XI, Université de

42

Soil Organic Carbon Degradation, Barrow, 2013-2014  

DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

This dataset provides information about soil organic carbon decomposition in Barrow soil incubation studies. The soil cores were collected from low-center polygon (Area A) and were incubated in the laboratory at different temperatures for up to 60 days. Transformations of soil organic carbon were characterized by UV and FT-IR, and small organic acids in water-soluble carbons were quantified by ion chromatography during the incubation

Baohua Gu; Ziming Yang

43

Carbon Dynamics in Aquatic Ecosystems in Response to Elevated Atmospheric CO2 and Altered Nutrients Availability  

E-Print Network [OSTI]

. Our results show that elevated CO2 led to enhanced photosynthetic carbon uptake and dissolved organic carbon (DOC) production. DOC occupied larger percentage in total organic carbon production in high CO2 environment. N addition stimulated biomass...

Song, Chao

2011-04-26T23:59:59.000Z

44

Unburned lubricant produces 60%90% of organic carbon emissions.  

E-Print Network [OSTI]

Unburned lubricant produces 60%­90% of organic carbon emissions. While diesel fuel is often viewed for gasoline light-duty vehicles are very effective at controlling organic carbon (OC) emissions. Diesel as the most polluting of conventional petroleum-based fuels, emissions from gasoline engines can more

45

The effect of mean cell residence time on the adsorbability of dissolved organic compounds found in petrochemical wastewaters  

E-Print Network [OSTI]

, each with a different mean cell residence time, biologically treated the waste- water. Follow1ng biolog1cal treatment, the wastewater was subjected to activated carbon adsorption treatment. The Freundlich isotherm, non-adsorbable organic compound... residence time on adsorbability is the same for petrochemical wastewater as it is for municipal wastewater. The purpose of this thesis is to determine if the mean cell residence time in a biological treatment process can af'feet the ad- sorbability...

Johnson, Timothy Loring

1979-01-01T23:59:59.000Z

46

Carbon isotope ratios of organic compound fractions in oceanic suspended particles  

E-Print Network [OSTI]

Radiocarbon evidence of fossil-carbon cycling in sediments1968), Metabolic fractionation of carbon isotopes in marineof particulate organic carbon using bomb 14 C, Nature,

Hwang, Jeomshik; Druffel, Ellen R. M

2006-01-01T23:59:59.000Z

47

Characterization and biodegradation of water-soluble biomarkers and organic carbon extracted from low temperature chars  

SciTech Connect (OSTI)

This study demonstrates that wildfires/biomass combustion may be an important source of labile pyrogenic water-soluble organic matter (Py-WSOM) to aquatic systems. Spectroscopic analysis (of the solid char and Py-WSOM) with Fourier transform infrared spectroscopy (FTIR) indicated that the Py-WSOM extracted from two low temperature chars (one wood, one grass) was dominated by polar moieties (-OH and C-O) derived from depolymerization and fragmentation of lignocellulose. Incubation experiments under aerobic conditions with unsterilized river water suggested that Py-WSOM and associated biomarkers may have turnover rates on the order of weeks to months, consistent with mixing and transport conditions of riverine systems. For example, pyrogenic dissolved organic carbon (Py-DOC) had a half-life of 30-40 days. Turnover rate for the combustion biomarkers was shorter, with levoglucosan and free lignin phenols having a half-life around 3-4 days and polymeric lignin components 13-14 days. The latter observations contradict earlier studies on the biodegradation of dissolved lignin and point to the need for re-assessment of lignin degradation kinetics in well-mixed riverine systems, particularly when such lignin components are derived from thermally altered plant material that may exist in a form more labile than that in highly processed riverine DOM.

Norwood, Matt J.; Louchouarn, Patrick; Kuo, Li-Jung; Harvey, Omar

2013-03-16T23:59:59.000Z

48

Management effects on labile organic carbon pools  

E-Print Network [OSTI]

It is well documented that increases in soil organic matter (SOM) improve soil physical properties and increase the overall fertility and sustainability of the soil. Research in SOM storage has recently amplified following the proposal...

Kolodziej, Scott Michael

2005-08-29T23:59:59.000Z

49

Sources and Fates of Dissolved Organic Carbon in Rural and Urban Watersheds in Brazos County, Texas  

E-Print Network [OSTI]

to frequent exposure to high sodium irrigation water. The results indicate that sodium is a major driver of DOC in the system. Sound management decisions concerning irrigation water chemistry and urban development might eventually emerge to protect water...

Cioce, Danielle

2012-10-19T23:59:59.000Z

50

Natural Abundance Radiocarbon Studies of Dissolved Organic Carbon (DOC) in the Marine Environment  

E-Print Network [OSTI]

Press, San Diego. Bruland, K.W. , (1989) Complexation of6624), 480-482. Rue, E.L. , Bruland, K.W. , (1997) The rolemetal binding ligands (Bruland, 1989; Rue and Bruland, 1997;

de Jesus, Roman P

2008-01-01T23:59:59.000Z

51

Natural abundance radiocarbon studies of dissolved organic carbon (DOC) in the marine environment  

E-Print Network [OSTI]

Press, San Diego. Bruland, K.W. , (1989) Complexation of6624), 480-482. Rue, E.L. , Bruland, K.W. , (1997) The rolemetal binding ligands (Bruland, 1989; Rue and Bruland, 1997;

De Jesus, Roman Paul

2008-01-01T23:59:59.000Z

52

Adsorption of dissolved organic carbon to mineral soils: A comparison of four isotherm approaches  

E-Print Network [OSTI]

.N. Kothawala a, , T.R. Moore a,1 , W.H. Hendershot b,2 a Department of Geography and Global Environmental

Moore, Tim

53

Uncorrected Latitudinal Trends in Organic Carbon  

E-Print Network [OSTI]

of freshwater wetlands to sequester C. Keywords Cesium-137 (137 Cs), climate change, Histosol, precipitation author: e-mail: ccraft@indiana.edu J. Vymazal (ed.), Wastewater Treatment, Plant Dynamics and Management relation- ships between climate (temperature) and C accumulation. Organic C accumulation was inversely

Craft, Christopher B.

54

RESEARCH ARTICLE Carbon quantity defines productivity while its quality defines  

E-Print Network [OSTI]

RESEARCH ARTICLE Carbon quantity defines productivity while its quality defines community that dissolved organic carbon (DOC) quantity and quality differently influence bacterioplankton. The ponds were production, abundance, biomass were highest in mid-summer and correlated positively with the concentration

Vincent, Warwick F.

55

Preservation of Organic Matter in Marine Sediments: Controls, Mechanisms, and an Imbalance in Sediment Organic Carbon Budgets?  

E-Print Network [OSTI]

Preservation of Organic Matter in Marine Sediments: Controls, Mechanisms, and an Imbalance in Sediment Organic Carbon Budgets? David J. Burdige* Department of Ocean, Earth and Atmospheric Sciences, Old.1. Organic Geochemistry of Marine Sediments: General Considerations 468 2. Molecularly Uncharacterized

Burdige, David

56

Highly dispersed carbon nanotubes in organic media for polymer:fullerene photovoltaic devices  

E-Print Network [OSTI]

Highly dispersed carbon nanotubes in organic media for polymer:fullerene photovoltaic devices Gwang photovoltaic device are fabricated using homogeneously dispersed carbon nanotubes (CNTs) in a polymer. All rights reserved. 1. Introduction Organic photovoltaic (OPV) materials promise the production

Hong, Soon Hyung

57

Emission and Chemistry of Organic Carbon in the Gas and Aerosol...  

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

and Chemistry of Organic Carbon in the Gas and Aerosol Phase at a Sub-Urban Site Near Mexico City in March 2006 During Emission and Chemistry of Organic Carbon in the Gas and...

58

Soil organic carbon sequestration potential of cropland in China Zhangcai Qin,1,2  

E-Print Network [OSTI]

Soil organic carbon sequestration potential of cropland in China Zhangcai Qin,1,2 Yao Huang,1), Soil organic carbon sequestration potential of cropland in China, Global Biogeochem. Cycles, 27, doi:10 carbon (SOC) in cropland is of great importance to the global carbon (C) balance and to agricultural

Pittendrigh, Barry

59

Extreme organic carbon burial fuels intense methane bubbling in a temperate reservoir  

E-Print Network [OSTI]

Extreme organic carbon burial fuels intense methane bubbling in a temperate reservoir Sebastian. Wehrli (2012), Extreme organic carbon burial fuels intense methane bubbling in a temperate reservoir; revised 25 November 2011; accepted 30 November 2011; published 4 January 2012. [1] Organic carbon (OC

Wehrli, Bernhard

60

Z .Marine Chemistry 67 1999 3342 Differences in seawater particulate organic carbon concentration  

E-Print Network [OSTI]

of the organic carbon retained by a glass-fiber filter against the volume filtered. The interceptZ .Marine Chemistry 67 1999 33­42 Differences in seawater particulate organic carbon concentration August 1998; accepted 11 May 1999 Abstract Z . Z . ZParticulate organic carbon POC data collected

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


61

Storage of Hydrogen, Methane, and Carbon Dioxide in Highly Porous Covalent Organic Frameworks for Clean Energy  

E-Print Network [OSTI]

, and carbon dioxide. Introduction Carbon dioxide emissions resulting from the burning of fossil fuels 20 metric tons of carbon dioxide per capita are released annually into the atmosphere.1a,b CarbonStorage of Hydrogen, Methane, and Carbon Dioxide in Highly Porous Covalent Organic Frameworks

Yaghi, Omar M.

62

Total organic carbon as an indicator of wood delignification  

SciTech Connect (OSTI)

Kraft pulping experiments were performed in a 12-liter electrically heated laboratory digester to determine pulp yields and residual lignin content (kappa number) as a function of time. Samples of the pulp and the black liquor were analyzed for total organic carbon (TOC) content by oxidizing the samples in a combustion furnace and measuring the released CO/sub 2/ gravimetrically. The experimental data on TOC were correlated with kappa number and yield. Results can be explained satisfactorily using a mathematical model based upon the principle of conservation of mass. The TOC content of black liquor appears to be a useful parameter for batch digester control. 17 references.

Genco, J.M.; Hassler, J.C.; Busayasakul, N.

1984-07-01T23:59:59.000Z

63

Atomic-Scale Detection of Organic Molecules Coupled to Single-Walled Carbon Nanotubes  

E-Print Network [OSTI]

Atomic-Scale Detection of Organic Molecules Coupled to Single-Walled Carbon Nanotubes Sung You Hong.green@chem.ox.ac.uk; ben.davis@chem.ox.ac.uk Functionalized carbon nanotubes (f-CNTs) bearing organic molecules functionalization of single-walled carbon nanotubes (SWNTs) can tailor critical proper- ties such as solubility

Davis, Ben G.

64

Organized Research Unit (ORU) on Carbon Capture and Sequestration: Meeting the Needs of the Energy Sector  

E-Print Network [OSTI]

Organized Research Unit (ORU) on Carbon Capture and Sequestration: Meeting the Needs of the Energy of an Organized Research Unit (ORU) on Carbon Capture and Sequestration (CCS). The purpose of this effort Frontier Research Center proposal: "Integrated Science of Geological Carbon Sequestration" to BES office

Zhou, Chongwu

65

Interaction effects of climate and land use/land cover change on soil organic carbon sequestration  

E-Print Network [OSTI]

Interaction effects of climate and land use/land cover change on soil organic carbon sequestration carbon sequestration Climate change Soil carbon change Historically, Florida soils stored the largest in Florida (FL) have acted as a sink for carbon (C) over the last 40 years. · Climate interacting with land

Grunwald, Sabine

66

REMOVAL OF ORGANIC POLLUTANTS FROM SUBCRITICAL WATER WITH ACTIVATED CARBON  

SciTech Connect (OSTI)

The Energy & Environmental Research Center (EERC) has demonstrated that controlling the temperature (and to a lesser extent, the pressure) of water can dramatically change its ability to extract organics and inorganics from matrices ranging from soils and sediments to waste sludges and coal. The dielectric constant of water can be changed from about 80 (a very polar solvent) to <5 (similar to a nonpolar organic solvent) by controlling the temperature (from ambient to about 400 C) and pressure (from about 5 to 350 bar). The EERC has shown that hazardous organic pollutants such as pesticides, PACS (polycyclic aromatic hydrocarbons), and PCBs (polychlorinated biphenyls) can be completely removed from soils, sludges, and sediments at temperatures (250 C) and pressures (<50 atm) that are much milder than typically used for supercritical water processes (temperature >374 C, pressure >221 atm). In addition, the process has been demonstrated to be particularly effective for samples containing very high levels of contaminants (e.g., part per thousand). Current projects include demonstrating the subcritical water remediation process at the pilot scale using an 8-liter system constructed under separate funding during 1997. To date, subcritical water has been shown to be an effective extraction fluid for removing a variety of organic pollutants from soils and sludges contaminated with fossil fuel products and waste products, including PACS from soil (e.g., town gas sites), refining catalysts, and petroleum tank bottom sludges; PCBs from soil and sediments; toxic gasoline components (e.g., benzene) from soil and waste sludge; and phenols from petroleum refinery sludges. The obvious need to clean the wastewater from subcritical water processes led to preliminary experiments with activated carbon placed in line after the extractor. Initial experiments were performed before and after cooling the extractant water (e.g., with water at 200 C and with water cooled to 25 C). Surprisingly, the ability of activated carbon to remove organics from the water is better at a high temperature than at room temperature. These initial results are opposite to those expected from chromatographic theory, since the solubility of the organics is about 100,000-fold higher in the hot water than in ambient water. At present, the physicochemical mechanism accounting for these results is unknown; however, it is possible that the lower surface tension and lower viscosity of subcritical water (compared to water at ambient conditions) greatly increases the available area of the carbon by several orders of magnitude. Regardless of the mechanism involved, the optimal use of activated carbon to clean the wastewater generated from subcritical water remediation will depend on obtaining a better understanding of the controlling parameters. While these investigations focused on the cleanup of wastewater generated from subcritical water remediation, the results also apply to cleanup of any wastewater contaminated with nonpolar and moderately polar organics such as wastewaters from coal and petroleum processing.

Steven B. Hawthorne; Arnaud J. Lagadec

1999-08-01T23:59:59.000Z

67

Differential Supply of Autochthonous Organic Carbon and Nitrogen to the Microbial Loop in the Delaware Estuary  

E-Print Network [OSTI]

Differential Supply of Autochthonous Organic Carbon and Nitrogen to the Microbial Loop to heterotrophic bacteria (bacteria) has been re-evaluated in the Delaware Estuary, considering carbon (C sources of organic matter to the estuarine microbial loop. Introduction The fate of organic matter

68

Liquid-phase adsorption of organic compounds by granular activated carbon and activated carbon fibers  

SciTech Connect (OSTI)

Liquid-phase adsorption of organic compounds by granular activated carbon (GAC) and activated carbon fibers (ACFs) is investigated. Acetone, isopropyl alcohol (IPA), phenol, and tetrahydrofuran (THF) were employed as the model compounds for the present study. It is observed from the experimental results that adsorption of organic compounds by GAC and ACF is influenced by the BET (Brunauer-Emmett-Teller) surface area of adsorbent and the molecular weight, polarity, and solubility of the adsorbate. The adsorption characteristics of GAC and ACFs were found to differ rather significantly. In terms of the adsorption capacity of organic compounds, the time to reach equilibrium adsorption, and the time for complete desorption, ACFs have been observed to be considerably better than GAC. For the organic compounds tested here, the GAC adsorptions were shown to be represented well by the Langmuir isotherm while the ACF adsorption could be adequately described by the Langmuir or the Freundlich isotherm. Column adsorption tests indicated that the exhausted ACFs can be effectively regenerated by static in situ thermal desorption at 150 C, but the same regeneration conditions do not do as well for the exhausted GAC.

Lin, S.H.; Hsu, F.M. [Yuan Ze Inst. of Tech., Taoyuan (Taiwan, Province of China). Dept. of Chemical Engineering

1995-06-01T23:59:59.000Z

69

PII S0016-7037(99)00361-0 Dissolved and particulate carbohydrates in contrasting marine sediments  

E-Print Network [OSTI]

PII S0016-7037(99)00361-0 Dissolved and particulate carbohydrates in contrasting marine sediments D) and mid-Atlantic shelf/slope break (continental margin) sediments. Particulate carbohydrates (PCHOs) rep- resented 5­9% of the total sediment particulate organic carbon (POC), and PCHO remineralization appeared

Burdige, David

70

Highly efficient carbon dioxide capture with a porous organic polymer impregnated with  

E-Print Network [OSTI]

Highly efficient carbon dioxide capture with a porous organic polymer impregnated environmental crises such as global warming and ocean acidication, efficient carbon dioxide (CO2) capture As CO2 capture mate- rials, numerous solid adsorbents such as silica5 and carbon materials,6 metal

Paik Suh, Myunghyun

71

Soil organic carbon enrichment of dust emissions: magnitude, mechanisms and its implications for  

E-Print Network [OSTI]

Soil organic carbon enrichment of dust emissions: magnitude, mechanisms and its implications Range, MSC 3 JER, NMSU, Box 30003, Las Cruces, NM 88003-8003, USA. E-mail: nwebb@nmsu.edu ABSTRACT: Soil to the role of aeolian processes in influencing soil organic carbon (SOC) flux and the release of greenhouse

72

Quantification of soil organic carbon using mid- and near- DRIFT spectroscopy  

E-Print Network [OSTI]

(X) and soil property data (Y) into a new smaller set of latent variables and their scores that best describe all the variance in the data. Oxidizable organic carbon content was measured by a modified Walkley-Black method, and total organic carbon...

Kang, Misun

2004-09-30T23:59:59.000Z

73

Carbon oxidation state as a metric for describing the chemistry of atmospheric organic aerosol  

SciTech Connect (OSTI)

A detailed understanding of the sources, transformations, and fates of organic species in the environment is crucial because of the central roles that organics play in human health, biogeochemical cycles, and Earth's climate. However, such an understanding is hindered by the immense chemical complexity of environmental mixtures of organics; for example, atmospheric organic aerosol consists of at least thousands of individual compounds, all of which likely evolve chemically over their atmospheric lifetimes. Here we demonstrate the utility of describing organic aerosol (and other complex organic mixtures) in terms of average carbon oxidation state (OSC), a quantity that always increases with oxidation, and is readily measured using state-of-the-art analytical techniques. Field and laboratory measurements of OSC , using several such techniques, constrain the chemical properties of the organics and demonstrate that the formation and evolution of organic aerosol involves simultaneous changes to both carbon oxidation state and carbon number (nC).

Massachusetts Institute of Technology; Kroll, Jesse H.; Donahue, Neil M.; Jimenez, Jose L.; Kessler, Sean H.; Canagaratna, Manjula R.; Wilson, Kevin R.; Altieri, Katye E.; Mazzoleni, Lynn R.; Wozniak, Andrew S.; Bluhm, Hendrik; Mysak, Erin R.; Smith, Jared D.; Kolb, Charles E.; Worsnop, Douglas R.

2010-11-05T23:59:59.000Z

74

Unexpected carbon-carbon coupling between organic cyanides and isopropyl {beta}-carbon in a hafnium ene diamide complex  

SciTech Connect (OSTI)

Reaction of the ene diamide complex Cp*Hf({sigma}{sup 2},{pi}-iPr-DAB)Cl (1; Cp* = {eta}{sup 5}-C{sub 5}Me{sub 5}, iPr-DAB = 1,4-diisopropyl-1,4-diaza-1,3-butadiene) with organic cyanides was investigated. The crystal structure of the product, Cp*Hf[iPrNCH{double_bond}CHNC(Me){double_bond}CHC(tBu){double_bond}NH]Cl, is reported. The reaction is thought to proceed by two hydrogen transfers and a C-C coupling on the {beta}-carbon of an isopropyl group. NMR was used to identify reaction intermediates in the hydrogen transfer scheme.

Bol, J.E.; Hessen, B.; Teuben, J.H. [Univ. of Groningen (Netherlands); Smeets, W.J.J.; Spek, A.L. [Univ. of Utrecht (Netherlands)

1992-06-01T23:59:59.000Z

75

Multi-Walled Carbon Nanotubes-Modified Polymer Organic Photovoltaics.  

E-Print Network [OSTI]

??Since the carbon nanotubes were first discovered by Iijima in 1991, CNTs have been the focus of intense research by many groups. Nearly 7000 papers… (more)

Chen, Tzu-Fan

2009-01-01T23:59:59.000Z

76

Constraining the propagation of bomb-radiocarbon through the dissolved organic carbon (DOC) pool in the northeast Pacific Ocean  

E-Print Network [OSTI]

the most recent series of thermonuclear tests. Nature 200 (Druffel, 1987) created by thermonuclear weapons testing inthe time elapsed since thermonuclear weapons testing ($50

Beaupré, Steven R; Druffel, Ellen R.M.

2009-01-01T23:59:59.000Z

77

Dissolved organic carbon (DOC) plays a central role in many aquatic ecosystem processes [e.g. (Williamson et al.,  

E-Print Network [OSTI]

. A study in North American lakes showed that photochemical degradation of DOC caused a decrease in UV radiation, especially UV radiation (UVR = 280­400 nm) (Scully and Lean, 1994; Morris et al., 1995). UVR can absorbance. Effects of photochemical degradation differed between lakes and were related to differences

Williamson, Craig E.

78

Polymer and carbon nanotube materials for chemical sensors and organic electronics  

E-Print Network [OSTI]

This thesis details the development of new materials for high-performance chemical sensing as well as organic electronic applications. In Chapter 2, we develop a chemiresistive material based on single-walled carbon nanotubes ...

Wang, Fei, Ph. D. Massachusetts Institute of Technology

2010-01-01T23:59:59.000Z

79

Highly efficient separation of carbon dioxide by a metal-organic framework replete with  

E-Print Network [OSTI]

Highly efficient separation of carbon dioxide by a metal-organic framework replete with open metal capture of CO2, which is essential for natural gas purifi- cation and CO2 sequestration, has been reported media. carbon dioxide capture dynamic adsorption reticular chemistry Selective removal of CO2 from

Yaghi, Omar M.

80

Limiting diffusion coefficients of heavy molecular weight organic contaminants in supercritical carbon dioxide  

E-Print Network [OSTI]

LIMITING DIFFUSION COEFFICIENTS OF HEAVY MOLECULAR WEIGHT ORGANIC CONTAMINANTS IN SUPERCRITICAL CARBON DIOXIDE A Thesis by MAURICIO OREJUELA Submitted to the Office of Graduate Studies of Texas A&M University in partial fulfillment... of the requirements for the degree of MASTER OF SCIENCE August 1994 Major Subject: Chemical Engineering LIMITING DIFFUSION COEFFICIENTS OF HEAVY MOLECULAR WEIGHT ORGANIC CONTAMINANTS IN SUPERCRITICAL CARBON DIOXIDE A Thesis by MAURICIO OREJUELA Submitted...

Orejuela, Mauricio

1994-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


81

Metal-Containing Organic and Carbon Aerogels for Hydrogen Storage  

SciTech Connect (OSTI)

This document and the accompanying manuscript summarize the technical accomplishments of our one-year LDRD-ER effort. Hydrogen storage and hydrogen fuel cells are important components of the 2003 Hydrogen Fuel Initiative focused on the reduction of America's dependence on oil. To compete with oil as an energy source, however, one must be able to transport and utilize hydrogen at or above the target set by DOE (6 wt.% H{sub 2}) for the transportation sector. Other than liquid hydrogen, current technology falls well short of this DOE target. As a result, a variety of materials have recently been investigated to address this issue. Carbon nanostructures have received significant attention as hydrogen storage materials due to their low molecular weight, tunable microporosity and high specific surface areas. For example, the National Renewable Energy Laboratory (NREL) achieved 5 to 10 wt.% H{sub 2} storage using metal-doped carbon nanotubes. That study showed that the intimate mix of metal nanoparticles with graphitic carbon resulted in the unanticipated hydrogen adsorption at near ambient conditions. The focus of our LDRD effort was the investigation of metal-doped carbon aerogels (MDCAs) as hydrogen storage materials. In addition to their low mass densities, continuous porosities and high surface areas, these materials are promising candidates for hydrogen storage because MDCAs contain a nanometric mix of metal nanoparticles and graphitic nanostructures. For FY04, our goals were to: (1) prepare a variety of metal-doped CAs (where the metal is cobalt, nickel or iron) at different densities and carbonization temperatures, (2) characterize the microstructure of these materials and (3) initiate hydrogen adsorption/desorption studies to determine H2 storage properties of these materials. Since the start of this effort, we have successfully prepared and characterized Ni- and Co-doped carbon aerogels at different densities and carbonization temperatures. The bulk of this work is described in the attached manuscript entitled 'Formation of Carbon Nanostructures in Cobalt- and Nickel- Doped Carbon Aerogels'. This one-year effort has lead to our incorporation into the DOE Carbon-based Hydrogen Storage Center of Excellence at NREL, with funding from DOE's Energy Efficiency and Renewable Energy (EERE) Program starting in FY05.

Satcher, Jr., J H; Baumann, T F; Herberg, J L

2005-01-10T23:59:59.000Z

82

Improved Detection of Bed Boundaries for Petrophysical Evaluation with Well Logs: Applications to Carbonate and Organic-Shale Formations  

E-Print Network [OSTI]

: Applications to Carbonate and Organic-Shale Formations Zoya Heidari, SPE, Texas A&M University and Carlos of well logs acquired in organic shales and carbonates is challenging because of the presence of thin beds acquired in thinly bedded carbonates and in the Haynesville shale-gas formation. Estimates of petrophysical

Torres-VerdĂ­n, Carlos

83

Oxygen production and carbon sequestration in an upwelling coastal Burke Hales,1  

E-Print Network [OSTI]

Oxygen production and carbon sequestration in an upwelling coastal margin Burke Hales,1 Lee Karp), Oxygen production and carbon sequestration in an upwelling coastal margin, Global Biogeochem. Cycles, 20 of particulate organic carbon (POC) and dissolved O2 during the upwelling season off the Oregon coast. Oxygen

Pierce, Stephen

84

August 22, 2002 Contribution to Stein, R. and Macdonald, R. W. (eds.) The Organic Carbon Cycle in  

E-Print Network [OSTI]

1 August 22, 2002 Contribution to Stein, R. and Macdonald, R. W. (eds.) The Organic Carbon Cycle. This problem is highlighted by a recent study of the carbon budget of the Mackenzie shelf by Macdonald et al

Eicken, Hajo

85

Substrate and environmental controls on microbial assimilation of soil organic carbon: a framework for Earth System Models  

SciTech Connect (OSTI)

Microbial assimilation of soil organic carbon is one of the fundamental processes of global carbon cycling and it determines the magnitude of microbial biomass in soils. Mechanistic understanding of microbial assimilation of soil organic carbon and its controls is important for to improve Earth system models ability to simulate carbon-climate feedbacks. Although microbial assimilation of soil organic carbon is broadly considered to be an important parameter, it really comprises two separate physiological processes: one-time assimilation efficiency and time-dependent microbial maintenance energy. Representing of these two mechanisms is crucial to more accurately simulate carbon cycling in soils. In this study, a simple modeling framework was developed to evaluate the substrate and environmental controls on microbial assimilation of soil organic carbon using a new term: microbial annual active period (the length of microbes remaining active in one year). Substrate quality has a positive effect on microbial assimilation of soil organic carbon: higher substrate quality (lower C:N ratio) leads to higher ratio of microbial carbon to soil organic carbon and vice versa. Increases in microbial annual active period from zero stimulate microbial assimilation of soil organic carbon; however, when microbial annual active period is longer than an optimal threshold, increasing this period decreases microbial biomass. The simulated ratios of soil microbial biomass to soil organic carbon are reasonably consistent with a recently compiled global dataset at the biome-level. The modeling framework of microbial assimilation of soil organic carbon and its controls developed in this study offers an applicable ways to incorporate microbial contributions to the carbon cycling into Earth system models for simulating carbon-climate feedbacks and to explain global patterns of microbial biomass.

Xu, Xiaofeng [ORNL] [ORNL; Schimel, Joshua [University of California, Santa Barbara] [University of California, Santa Barbara; Thornton, Peter E [ORNL] [ORNL; Song, Xia [ORNL] [ORNL; Yuan, Fengming [ORNL] [ORNL; Goswami, Santonu [ORNL] [ORNL

2014-01-01T23:59:59.000Z

86

The distribution of organic carbon in the Brazos River basin  

E-Print Network [OSTI]

of 6. 12 mgC/1 for a station in Brazoria County. This sample was taken 8 April 1962 and was analyzed by an infrared method. This method consists of: (1) removing all inorganic carbonate from a sample of water by acidifying the sample and pass- ing... is often too saline. The salt load of the Brazos River comes from the entire basin and is the result of solution, accretion of un- determined amounts of oil-field brine, and accretion of brine from springs and seeps---such as those in Salt Croton Creek...

Brooks, James Mark

1970-01-01T23:59:59.000Z

87

Thermoelectric Behavior of Flexible Organic Nanocomposites with Carbon Nanotubes  

E-Print Network [OSTI]

with ~100 S/m of electrical conductivity, resulting ~10,000 µW/m-K2 of power factor. The result of this study shows that organic thermoelectric materials would be a promising approach for thermoelectric applications with light-weight and non-toxic nature....

Choi, Kyung Who

2013-12-03T23:59:59.000Z

88

Adsorption -capacity data for 283 organic compounds  

SciTech Connect (OSTI)

Adsorption on activated carbon is a widely used method for removing volatile organic compounds (VOCs) from gases and other exhaust streams. This article presents a compilation of adsorption-capacity data as a function of the VOC concentration in the gas. The results are useful in engineering and environmental studies, and in the design of carbon-based adsorption systems to remove unwanted organic pollutants from gases. For vapor control, carbon-based systems typically combine a carbon-adsorption unit with a secondary control method to reclaim or destroy the vapors desorbed during carbon-bed regeneration. To remove organics dissolved in wastewater, air stripping is typically used to transfer the organics to a vapor stream. Carbon adsorption is then used to separate the organics from the stripper exhaust. Collected vapors can be recovered for reuse or destroyed, depending on their value.

Yaws, C.L.; Bu, L.; Nijhawan, S. [Lamar Univ., Beaumont, TX (United States)

1995-05-01T23:59:59.000Z

89

Simulating Field-Scale Soil Organic Carbon Dynamics Using EPIC  

SciTech Connect (OSTI)

Simulation models integrate our knowledge of soil organic C (SOC) dynamics and are useful tools for evaluating impacts of crop management on soil C sequestration; yet, they require local calibration. Our objectives were to calibrate the Environmental Policy Integrated Climate (EPIC) model, and evaluate its performance for simulating SOC fractions as affected by soil landscape and management. An automated parameter optimization procedure was used to calibrate the model for a site-specific experiment in the Coastal Plain of central Alabama. The ability of EPIC to predict corn (Zea mays L.) and cotton (Gossypium hirsutum L.) yields and SOC dynamics on different soil landscape positions (summit, sideslope and drainageway) during the initial period of conservation tillage adoption (5 years) was evaluated using regression and mean squared deviations. Simulated yield explained 88% of measured yield variation, with greatest disagreement on the sideslope position and highest agreement in the drainageway. Simulations explained approximately 1, 34 and 40% of the total variation in microbial biomass C (MBC), particulate organic C (POC) and total organic C (TOC), respectively. Lowest errors on TOC simulations (0-20 cm) were found on the sideslope and summit. We conclude that the automated parameterization was generally successful, although further work is needed to refine the MBC and POC fractions, and to improve EPIC predictions of SOC dynamics with depth. Overall, EPIC was sensitive to spatial differences in C fractions that resulted from differing soil landscape positions. The model needs additional refinement for accurate simulations of field-scale SOC dynamics affected by short-term management decisions.

Causarano, Hector J.; Shaw, Joey N.; Franzluebbers, A. J.; reeves, D. W.; Raper, Randy L.; Balkcom, Kipling S.; Norfleet, M. L.; Izaurralde, R Cesar

2007-07-01T23:59:59.000Z

90

Relationship between Compost Stability and Extractable Organic Carbon L. Wu and L. Q. Ma*  

E-Print Network [OSTI]

OH-extractable organic carbon (OC) containsfor a better compost quality control and utilization efficiency. The objective found that the OC contentOC concentration was influenced by the total volatile solids and de- of the core HA relative to total dry mass increased whilecreased with curing time for compost with a high

Ma, Lena

91

Organic carbon sources and transformations in mangrove sediments: A Rock-Eval pyrolysis approach  

E-Print Network [OSTI]

Organic carbon sources and transformations in mangrove sediments: A Rock-Eval pyrolysis approach C'Orléans, CNRS/INSU, Université d'Orléans, 1A rue de la Férollerie, 45071 Orléans, France Abstract A Rock cycling in this specific environment using a method that allows monitoring the depth evolution of sources

Paris-Sud XI, Université de

92

Organic carbon burial efficiency in lake sediments controlled by oxygen exposure time and sediment source  

E-Print Network [OSTI]

Organic carbon burial efficiency in lake sediments controlled by oxygen exposure time and sediment : deposited OC) in a diverse set of 27 different sediments from 11 lakes, focusing on the potential effects burial efficiency was high (mean 48%), and it was particularly high in sediments receiving high input

Wehrli, Bernhard

93

Identification of Sediment Organic Carbon Location and Association with Polycyclic Aromatic Hydrocarbons (PAHs) in Contaminated Sediment  

E-Print Network [OSTI]

Identification of Sediment Organic Carbon Location and Association with Polycyclic Aromatic Hydrocarbons (PAHs) in Contaminated Sediment Upal Ghosh1 , Richard G. Luthy1 , J. Seb Gillette2 , and Richard N long-term issue confronting sediment bioremediation is the lack of understanding of contaminant-sediment

94

LAND USE AND PARENT MATERIAL EFFECTS ON SOIL ORGANIC CARBON AND NITROGEN IN THE  

E-Print Network [OSTI]

LAND USE AND PARENT MATERIAL EFFECTS ON SOIL ORGANIC CARBON AND NITROGEN IN THE KONYA BASIN, TURKEY AND NITROGEN IN THE KONYA BASIN, TURKEY: METHODS AND DATA FOR LANDSCAPE-SCALE ENVIRONMENTAL MONITORING Marc T use practices and soil parent materials on soil biogeochemistry in the Konya Basin, south

Wisconsin at Madison, University of

95

REGULAR ARTICLE Alfalfa-grass biomass, soil organic carbon, and total nitrogen  

E-Print Network [OSTI]

REGULAR ARTICLE Alfalfa-grass biomass, soil organic carbon, and total nitrogen under different and N content in alfalfa-grass mixture, and their relationships with SOC and STN. Methods An alfalfa-/belowground allocation changed seasonally. Keywords Aboveground biomass . Root biomass . Alfalfa-grasses cropping . Soil

Norton, Jay B.

96

Deep-Sea Research II 50 (2003) 655674 Determining true particulate organic carbon: bottles, pumps  

E-Print Network [OSTI]

Deep-Sea Research II 50 (2003) 655­674 Determining true particulate organic carbon: bottles, pumps or by in situ filtration with pumps and analyzing the filters. The concentrations measured by these two methods-latitude waters. Here we report that the ratio of bottle POC to pump POC ranged between 20 and 200 in the Ross Sea

Hansell, Dennis

97

Optical Properties of Mixed Black Carbon, Inorganic and Secondary Organic Aerosols  

SciTech Connect (OSTI)

Summarizes the achievements of the project, which are divided into four areas: 1) Optical properties of secondary organic aerosols; 2) Development and of a polar nephelometer to measure aerosol optical properties and theoretical approaches to several optical analysis problems, 3) Studies on the accuracy of measurements of absorbing carbon by several methods, and 4) Environmental impacts of biodiesel.

Paulson, S E

2012-05-30T23:59:59.000Z

98

An extended organic carbon-isotope record across the TriassicJurassic boundary in the Queen Charlotte Islands,  

E-Print Network [OSTI]

a negative offset in baseline carbon isotope values from approximately -29 in the Late Norian to -31An extended organic carbon-isotope record across the Triassic­Jurassic boundary in the Queen carbon-isotope data are presented for the Triassic­Jurassic boundary section at Kennecott Point, Queen

Williford, Kenneth H.

99

Metal-Organic Frameworks with Precisely Designed Interior for Carbon Dioxide Capture in the Presence of Water  

E-Print Network [OSTI]

Metal-Organic Frameworks with Precisely Designed Interior for Carbon Dioxide Capture preservation of the IRMOF structure. Carbon dioxide capture from combustion sources such as flue gas in power this carbon capture challenge. The preferred method for measuring the efficiency of a given material

Yaghi, Omar M.

100

Layered Organic Structure at the Carbon Tetrachloride-Water Interface Dennis K. Hore, Dave S. Walker, and Geraldine L. Richmond*  

E-Print Network [OSTI]

Layered Organic Structure at the Carbon Tetrachloride-Water Interface Dennis K. Hore, Dave S remediation. The carbon tetrachloride-water interface in particular has been the subject of numerous the density profile across the interface. No detailed studies of the carbon tetrachloride structure

Richmond, Geraldine L.

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


101

Li+ solvation in pure, binary and ternary mixtures of organic carbonate electrolytes  

E-Print Network [OSTI]

Classical molecular dynamics (MD) simulations and quantum chemical density functional theory (DFT) calculations have been employed in the present study to investigate the solvation of lithium cations in pure organic carbonate solvents (ethylene carbonate (EC), propylene carbonate (PC) and dimethyl carbonate (DMC)) and their binary (EC-DMC, 1:1 molar composition) and ternary (EC-DMC-PC, 1:1:3 molar composition) mixtures. The results obtained by both methods indicate that the formation of complexes with four solvent molecules around Li+, exhibiting a strong local tetrahedral order, is the most favorable. However, the molecular dynamics simulations have revealed the existence of significant structural heterogeneities, extending up to a length scale which is more than five times the size of the first coordination shell radius. Due to these significant structural fluctuations in the bulk liquid phases, the use of larger size clusters in DFT calculations has been suggested. Contrary to the findings of the DFT calcu...

Skarmoutsos, Ioannis; Vetere, Valentina; Mossa, Stefano

2014-01-01T23:59:59.000Z

102

Photoconductive CdSe Nanowire Arrays, Serpentines, and Loops Formed by Electrodeposition on Self-Organized Carbon Nanotubes  

E-Print Network [OSTI]

Photoconductive CdSe Nanowire Arrays, Serpentines, and Loops Formed by Electrodeposition on Self-Organized Carbon Nanotubes X. Wendy Gu,,§ Nitzan Shadmi, Tohar S. Yarden,, Hagai Cohen, and Ernesto Joselevich with controlled geometries by using self-organized single-walled carbon nanotubes as a template for the selective

Joselevich, Ernesto

103

In Situ Infrared Spectroscopic Study of Brucite Carbonation in...  

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

Carbonation in Dry to Water-Saturated Supercritical Carbon Dioxide. Abstract: In geologic carbon sequestration, while part of the injected carbon dioxide will dissolve into host...

104

Effects of organic carbon supply rates on mobility of previously bioreduced uranium in a contaminated sediment  

E-Print Network [OSTI]

contaminated subsurface sediments. Environ. Microbiol. 2002,in previously bioreduced sediment by dissolved oxygen andcontaminated aquifer sediments. Appl Environ Microbiol 2002,

Wan, J.

2008-01-01T23:59:59.000Z

105

1 Protection of Organic Carbon in Soil Microaggregates Occurs via Restructuring of Aggregate Porosity and Filling of Pores with Accumulating Organic Matter  

E-Print Network [OSTI]

1 Protection of Organic Carbon in Soil Microaggregates Occurs via Restructuring of Aggregate, and comparison of its extent among treatments suggests important feedback loops. The 41 use of USAXS, which has, and insights relevant to strategies for enhancing 44 carbon-sequestration in soil through changes

McCarthy, John F.

106

The effects of water on the passive behavior of 1018 carbon steel in organic solutions  

SciTech Connect (OSTI)

The passivation and breakdown behavior of 1018 carbon steel in propylene carbonate (PC) or dimethoxyethane (DME) mixtures with water and containing 0.5M LiAsF[sub 6] were studied. The behavior of the steel in the organic solvent/water mixtures was highly dependent on the organic solvent. The anodic polarization of carbon steel displayed active-passive behavior in 10--90 mole percent (m/o) PC/H[sub 2]O mixtures and a tenuous degree of stability within the passive range. The anodic polarization of carbon steel displayed no active-passive behavior in 50--90 m/o DME/H[sub 2]O mixtures and displayed active-passive behavior in 10--30 m/o DME/H[sub 2]O mixtures. The steel was stable within the passive range of these DME/H[sub 2]O solutions. The breakdown potential of the steel in DME/H[sub 2]O mixtures is more electropositive than the oxidation potential of the DME solvent at all molar ratios.

Shifler, D.A.; Kruger, J. (John Hopkins Univ., Baltimore, MD (United States). Dept. of Materials Science and Engineering); Moran, P.J. (Naval Academy, Annapolis, MD (United States). Dept. of Mechanical Engineering)

1994-04-01T23:59:59.000Z

107

T E C H N I C A L A D V A N C E Soil organic carbon dust emission: an omitted global  

E-Print Network [OSTI]

T E C H N I C A L A D V A N C E Soil organic carbon dust emission: an omitted global source emission, soil organic carbon Received 16 April 2013 and accepted 21 May 2013 Introduction Uncertainty, Gunnedah, NSW 2380, Australia Abstract Soil erosion redistributes soil organic carbon (SOC) within

108

Improved thermoelectric power output from multilayered polyethylenimine doped carbon nanotube based organic composites  

SciTech Connect (OSTI)

By appropriately selecting the carbon nanotube type and n-type dopant for the conduction layers in a multilayered carbon nanotube composite, the total device thermoelectric power output can be increased significantly. The particular materials chosen in this study were raw single walled carbon nanotubes for the p-type layers and polyethylenimine doped single walled carbon nanotubes for the n-type layers. The combination of these two conduction layers leads to a single thermocouple Seebeck coefficient of 96 ± 4??VK{sup ?1}, which is 6.3 times higher than that previously reported. This improved Seebeck coefficient leads to a total power output of 14.7 nW per thermocouple at the maximum temperature difference of 50?K, which is 44 times the power output per thermocouple for the previously reported results. Ultimately, these thermoelectric power output improvements help to increase the potential use of these lightweight, flexible, and durable organic multilayered carbon nanotube based thermoelectric modules in low powered electronics applications, where waste heat is available.

Hewitt, Corey A.; Montgomery, David S.; Barbalace, Ryan L.; Carlson, Rowland D.; Carroll, David L., E-mail: carroldl@wfu.edu [Center for Nanotechnology and Molecular Materials, Wake Forest University, 501 Deacon Blvd., Winston Salem, North Carolina 27105 (United States)

2014-05-14T23:59:59.000Z

109

Partitioning Behavior of Organic Contaminants in Carbon Storage Environments: A Critical Review  

SciTech Connect (OSTI)

Carbon capture and storage is a promising strategy for mitigating the CO{sub 2} contribution to global climate change. The large scale implementation of the technology mandates better understanding of the risks associated with CO{sub 2} injection into geologic formations and the subsequent interactions with groundwater resources. The injected supercritical CO{sub 2} (sc-CO{sub 2}) is a nonpolar solvent that can potentially mobilize organic compounds that exist at residual saturation in the formation. Here, we review the partitioning behavior of selected organic compounds typically found in depleted oil reservoirs in the residual oil–brine–sc-CO{sub 2} system under carbon storage conditions. The solubility of pure phase organic compounds in sc-CO{sub 2} and partitioning of organic compounds between water and sc-CO{sub 2} follow trends predicted based on thermodynamics. Compounds with high volatility and low aqueous solubility have the highest potential to partition to sc-CO{sub 2}. The partitioning of low volatility compounds to sc-CO{sub 2} can be enhanced by co-solvency due to the presence of higher volatility compounds in the sc-CO{sub 2}. The effect of temperature, pressure, salinity, pH, and dissolution of water molecules into sc-CO{sub 2} on the partitioning behavior of organic compounds in the residual oil-brine-sc-CO{sub 2} system is discussed. Data gaps and research needs for models to predict the partitioning of organic compounds in brines and from complex mixtures of oils are presented. Models need to be able to better incorporate the effect of salinity and co-solvency, which will require more experimental data from key classes of organic compounds.

Burant, Aniela; Lowry, Gregory V.; Karamalidis, Athanasios K.

2013-01-01T23:59:59.000Z

110

An assessment of particulate organic carbon to thorium-234 ratios in the ocean and their impact on the application  

E-Print Network [OSTI]

An assessment of particulate organic carbon to thorium-234 ratios in the ocean and their impact February 2006 Abstract Thorium-234 is increasingly used as a tracer of ocean particle flux, primarily

Coppola, Laurent

111

Dissolved Oxygen in Allen CreekDissolved Oxygen in Allen Creek Dissolved oxygen (DO) enters the water by diffusion from air, as a by-product of photosynthesis and  

E-Print Network [OSTI]

Dissolved Oxygen in Allen CreekDissolved Oxygen in Allen Creek Dissolved oxygen (DO) enters and rapids. There is an inverse relationship between temperature and DO, i.e. colder water holds more oxygen it supplies oxygen to aquatic organisms. Higher DO levels also give the water a better taste. Figure 2. During

Tyler, Christy

112

CVD Growth of Self-Organized Micro-Honeycomb Network Structure of Single-Walled Carbon Nanotubes for Photovoltaic Devices  

E-Print Network [OSTI]

CVD Growth of Self-Organized Micro-Honeycomb Network Structure of Single-Walled Carbon Nanotubes of dye-sensitized solar cells. Here, we propose a self-organized micro-honeycomb network structure performance. The SWNT/n-Si heterojunction solar cell was built by placing the micro-honeycomb SWNTs network

Maruyama, Shigeo

113

Mobilization and Transport of Organic Compounds from Reservoir Rock and Caprock in Geological Carbon Sequestration Sites  

SciTech Connect (OSTI)

Supercritical CO2 (scCO2) is an excellent solvent for organic compounds, including benzene, toluene, ethyl-benzene, and xylene (BTEX), phenols, and polycyclic aromatic hydrocarbons (PAHs). Monitoring results from geological carbon sequestration (GCS) field tests has shown that organic compounds are mobilized following CO2 injection. Such results have raised concerns regarding the potential for groundwater contamination by toxic organic compounds mobilized during GCS. Knowledge of the mobilization mechanism of organic compounds and their transport and fate in the subsurface is essential for assessing risks associated with GCS. Extraction tests using scCO2 and methylene chloride (CH2Cl2) were conducted to study the mobilization of volatile organic compounds (VOCs, including BTEX), the PAH naphthalene, and n-alkanes (n-C20 – n-C30) by scCO2 from representative reservoir rock and caprock obtained from depleted oil reservoirs and coal from an enhanced coal-bed methane recovery site. More VOCs and naphthalene were extractable by scCO2 compared to the CH2Cl2 extractions, while scCO2 extractable alkane concentrations were much lower than concentrations extractable by CH2Cl2. In addition, dry scCO2 was found to extract more VOCs than water saturated scCO2, but water saturated scCO2 mobilized more naphthalene than dry scCO2. In sand column experiments, moisture content was found to have an important influence on the transport of the organic compounds. In dry sand columns the majority of the compounds were retained in the column except benzene and toluene. In wet sand columns the mobility of the BTEX was much higher than that of naphthalene. Based upon results determined for the reservoir rock, caprock, and coal samples studied here, the risk to aquifers from contamination by organic compounds appears to be relatively low; however, further work is necessary to fully evaluate risks from depleted oil reservoirs.

Zhong, Lirong; Cantrell, Kirk J.; Mitroshkov, Alexandre V.; Shewell, Jesse L.

2014-05-06T23:59:59.000Z

114

PROCESS WATER RECOVERY: DISSOLVED AIR FLOTATION COMPARED TO HIGH SHEAR RATE SEPARATION  

E-Print Network [OSTI]

PROCESS WATER RECOVERY: DISSOLVED AIR FLOTATION COMPARED TO HIGH SHEAR RATE SEPARATION John H to the feed without dissolved air or with the addition of dual polymer flocculating polymers. Although fiber intend to investigate the effect of pacifying stickies by precipitating calcium carbonate with carbon

Abubakr, Said

115

Oceanography June 200450 Colored Dissolved Organic  

E-Print Network [OSTI]

blue sea" can typically be seen only hundreds of miles offshore. The areas of the ocean that most that are by products of plant and animal decompo- sition, and can come from both terrestrial and marine sources. When of the Mississippi River just offshore of where it enters the Gulf of Mexico. The brown color observed from a Paula

Oregon, University of

116

Rare earth element concentrations and speciation in organic-rich blackwaters of the Great Dismal Swamp, Virginia, USA  

E-Print Network [OSTI]

Rare earth element concentrations and speciation in organic-rich blackwaters of the Great Dismal Concentrations of rare earth elements (REE), major inorganic solutes, and dissolved organic carbon (DOC) were reserved. Keywords: Rare earth elements; Speciation; Humic substances; Geochemistry; Great Dismal Swamp

Burdige, David

117

The Stability of Organic Solvents and Carbon Electrode in Nonaqueous Li-O2 Batteries  

SciTech Connect (OSTI)

The effect of different kinds of aprotic organic solvents on the discharge performance and discharge products in Li-O2 batteries was systematically investigated. The discharge products deposited in air cathodes were analyzed by X-ray diffraction, in situ gas chromatography/mass spectroscopy and X-ray photoelectron spectroscopy. We found that a significant amount of Li2O2 can be formed in glyme-based electrolytes during the discharge process, while only small amount of Li2O2 is produced in electrolytes of phosphate, nitrile, ionic liquid and sulfoxide. However, in all the seven types of solvent systems we studied, Li2CO3 and LiF were still formed as byproducts whose compositions are strongly related to the solvents. Li2CO3 is produced not from the carbon air electrode but from oxidation and decomposition of the solvent as we verified by using a 13C-labeled carbon electrode and the solid-state 13C-MAS NMR technique. The formation of Li2CO3 and LiF during discharge will greatly reduce the Coulombic efficiency and cycle life of the Li-air batteries. Therefore, better electrolytes that can ensure the formation of Li2O2 but minimize other reaction products formed on air electrodes of Li-air batteries need to be further investigated.

Xu, Wu; Hu, Jian Z.; Engelhard, Mark H.; Towne, Silas A.; Hardy, John S.; Xiao, Jie; Feng, Ju; Hu, Mary Y.; Zhang, Jian; Ding, Fei; Gross, Mark E.; Zhang, Jiguang

2012-05-18T23:59:59.000Z

118

Photocatalytic and chemical oxidation of organic compounds in supercritical carbon dioxide. Progress report for FY97  

SciTech Connect (OSTI)

'The background for the project is briefly reviewed and the work done during the nine months since funding was received is documented. Work began in January, 1997. A post doctoral fellow joined the team in April. The major activities completed this fiscal year were: staffing the project, design of the experimental system, procurement of components, assembly of the system. preparation of the Safe Operating Procedure and ES and H compliance, pressure testing, establishing data collection and storage methodology, and catalyst preparation. Objective The objective of the project is to develop new chemistry for the removal of organic contaminants from supercritical carbon dioxide. This has application in processes used for continuous cleaning and extraction of parts and waste materials. A secondary objective is to increase the fundamental understanding of photocatalytic chemistry. Cleaning and extraction using supercritical carbon dioxide (scCO{sub 2}) can be applied to the solution of a wide range of environmental and pollution prevention problems in the DOE complex. Work is being done that explores scCO{sub 2} in applications ranging from cleaning contaminated soil to cleaning components constructed from plutonium. The rationale for use of scCO{sub 2} are based on the benign nature, availability and low cost, attractive solvent properties, and energy efficient separation of the extracted solute from the solvent by moderate temperature or pressure changes. To date, R and D has focussed on the methods and applications of the extraction steps of the process. Little has been done that addresses methods to polish the scCO{sub 2} for recycle in the cleaning or extraction operations. In many applications it will be desirable to reduce the level of contamination from that which would occur at steady state operation of a process. This proposal addresses chemistry to achieve that. This would be an alternative to removing a fraction of the contaminated scCO{sub 2} for disposal and using makeup scCO{sub 2}. A chemical polishing operation can reduce the release of CO{sub 2} from the process. It can also reduce the consumption of reagents that may be used in the process to enhance extraction and cleaning. A polishing operation will also reduce or avoid formation of an additional waste stream. Photocatalytic and other photochemical oxidation chemistry have not been investigated in scCO{sub 2}. The large base of information for these reactions in water, organic solvents, or air suggest that the chemistry will work in carbon dioxide. There are compelling reasons to believe that the properties of scCO{sub 2} should increase the performance of photocatalytic chemistry over that found in more conventional fluid phases.'

Blake, D.M.; Bryant, D.L.; Reinsch, V.

1997-09-30T23:59:59.000Z

119

PII S0016-7037(99)00335-X Sedimentary sources of old high molecular weight dissolved organic carbon from the ocean  

E-Print Network [OSTI]

and Bruland, 1988; Rue and Bruland, 1997). The processes which control the cycling of DOC in the ocean

Guo, Laodong

120

Assessment of temporal patterns in dissolved organic carbon in Tempe Town Lake Monica M. Palta1 and Hilairy E.Hartnett1,2  

E-Print Network [OSTI]

· Explore potential for monitoring some component of phytoplankton/community respiration or NPP that can symbols, city of Tempe Time Series Data · Tempe Town Lake was constructed in 1999, and provides recreation

Hall, Sharon J.

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


121

Capture of Carbon Dioxide from Air and Flue Gas in the Alkylamine-Appended Metal-Organic Framework mmen-Mg2(dobpdc)  

E-Print Network [OSTI]

, stationary sources like coal-fired power plants, carbon capture and sequestration (CCS) has been proposed.4Capture of Carbon Dioxide from Air and Flue Gas in the Alkylamine- Appended Metal-Organic Framework viable absorbents for carbon capture under the aforementioned conditions, and they are presently used

122

Carbon Nanosheets and Nanostructured Electrodes in Organic Photovoltaic Devices: Cooperative Research and Development Final Report, CRADA Number CRD-08-321  

SciTech Connect (OSTI)

Carbon nanosheet thin films were employed as nanostructured electrodes in organic solar cells. Due to the nanostructured texture of the carbon nanosheet electrodes, there was an increase in performance over standard ITO electrodes with very thick active layers. ZnO deposited via atomic layer deposition (ALD) was used as a hole blocking layer to provide for carrier selectivity of the carbon nanosheets.

Olson, D.

2012-04-01T23:59:59.000Z

123

Carbon dioxide effects research and assessment program: flux of organic carbon by rivers to the oceans. [Lead abstract  

SciTech Connect (OSTI)

Separate abstracts were prepared for the 15 papers presented in this workshop report. The state of knowledge about the role of rivers in the transport, storage and oxidation of carbon is the subject of this report. (KRM)

None

1981-04-01T23:59:59.000Z

124

Black carbon in the Gulf of Maine : new insights into inputs and cycling of combustion-derived organic carbon  

E-Print Network [OSTI]

Emissions of black carbon (BC), the soot and char formed during incomplete combustion of fossil and biomass fuels, have increased over the last century and are estimated to be between 8 and 270 Tg BC/yr. BC may affect ...

Flores Cervantes, Déborah Xanat, 1978-

2008-01-01T23:59:59.000Z

125

Low Power, Red, Green and Blue Carbon Nanotube Enabled Vertical Organic Light Emitting Transistors for Active Matrix OLED Displays  

SciTech Connect (OSTI)

Organic semiconductors are potential alternatives to polycrystalline silicon as the semiconductor used in the backplane of active matrix organic light emitting diode displays. Demonstrated here is a light-emitting transistor with an organic channel, operating with low power dissipation at low voltage, and high aperture ratio, in three colors: red, green and blue. The single-wall carbon nanotube network source electrode is responsible for the high level of performance demonstrated. A major benefit enabled by this architecture is the integration of the drive transistor, storage capacitor and light emitter into a single device. Performance comparable to commercialized polycrystalline-silicon TFT driven OLEDs is demonstrated.

McCarthy, M. A. [University of Florida, Gainesville; Liu, B. [University of Florida, Gainesville; Donoghue, E. P. [University of Florida, Gainesville; Kravchenko, Ivan I [ORNL; Kim, D. Y. [University of Florida, Gainesville; So, Franky [University of Florida, Gainesville; Rinzler, A. G. [University of Florida, Gainesville

2011-01-01T23:59:59.000Z

126

E-Print Network 3.0 - acyclic organic carbonate Sample Search...  

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

(PAN... ORNL 2011-G00246jcn UT-B ID 200501518 09.2011 System to Continuously Produce Carbon Fiber via... developed at ORNL, carbon fibers with specific mechanical properties...

127

The Effects of Moisture and Organic Matter Lability on Carbon Dioxide and Methane Production in an  

E-Print Network [OSTI]

amounts of carbon in the form of peat and other undecomposed plant matter. Global climate change al. 2003). The carbon stored in wetlands is in the form of undecayed plant matter, or peat. Peat carbon are very useful for agricultural purposes. Their peat and preserved timber has been mined

Vallino, Joseph J.

128

Composite Membranes for CO2 Capture: High Performance Metal Organic Frameworks/Polymer Composite Membranes for Carbon Dioxide Capture  

SciTech Connect (OSTI)

IMPACCT Project: A team of six faculty members at Georgia Tech are developing an enhanced membrane by fitting metal organic frameworks, compounds that show great promise for improved carbon capture, into hollow fiber membranes. This new material would be highly efficient at removing CO2 from the flue gas produced at coal-fired power plants. The team is analyzing thousands of metal organic frameworks to identify those that are most suitable for carbon capture based both on their ability to allow coal exhaust to pass easily through them and their ability to select CO2 from that exhaust for capture and storage. The most suitable frameworks would be inserted into the walls of the hollow fiber membranes, making the technology readily scalable due to their high surface area. This composite membrane would be highly stable, withstanding the harsh gas environment found in coal exhaust.

None

2010-07-01T23:59:59.000Z

129

SciTech Connect: Worldwide organic soil carbon and nitrogen data  

Office of Scientific and Technical Information (OSTI)

and geographic soil-forming factors. Therefore, information is included on location, soil nitrogen content, climate, and vegetation along with carbon density and variation....

130

Process for producing organic products containing silicon, hydrogen, nitrogen, and carbon by the direct reaction between elemental silicon and organic amines and products formed thereby  

DOE Patents [OSTI]

A process is disclosed for producing, at a low temperature, a high purity organic reaction product consisting essentially of silicon, hydrogen, nitrogen, and carbon. The process comprises reacting together a particulate elemental high purity silicon with a high purity reactive amine reactant in a liquid state at a temperature of from about O/degree/C up to about 300/degree/C. A high purity silicon carbide/silicon nitride ceramic product can be formed from this intermediate product, if desired, by heating the intermediate product at a temperature of from about 1200-1700/degree/C for a period from about 15 minutes up to about 2 hours or the organic reaction product may be employed in other chemical uses.

Pugar, E.A.; Morgan, P.E.D.

1988-04-04T23:59:59.000Z

131

DISSOLVED CONCENTRATION LIMITS OF RADIOACTIVE ELEMENTS  

SciTech Connect (OSTI)

The purpose of this study is to evaluate dissolved concentration limits (also referred to as solubility limits) of elements with radioactive isotopes under probable repository conditions, based on geochemical modeling calculations using geochemical modeling tools, thermodynamic databases, field measurements, and laboratory experiments. The scope of this modeling activity is to predict dissolved concentrations or solubility limits for 14 elements with radioactive isotopes (actinium, americium, carbon, cesium, iodine, lead, neptunium, plutonium, protactinium, radium, strontium, technetium, thorium, and uranium) important to calculated dose. Model outputs for uranium, plutonium, neptunium, thorium, americium, and protactinium are in the form of tabulated functions with pH and log (line integral) CO{sub 2} as independent variables, plus one or more uncertainty terms. The solubility limits for the remaining elements are either in the form of distributions or single values. The output data from this report are fundamental inputs for Total System Performance Assessment for the License Application (TSPA-LA) to determine the estimated release of these elements from waste packages and the engineered barrier system. Consistent modeling approaches and environmental conditions were used to develop solubility models for all of the actinides. These models cover broad ranges of environmental conditions so that they are applicable to both waste packages and the invert. Uncertainties from thermodynamic data, water chemistry, temperature variation, and activity coefficients have been quantified or otherwise addressed.

NA

2004-11-22T23:59:59.000Z

132

The Dissolution of Desicooler Residues in H-Canyon Dissolvers  

SciTech Connect (OSTI)

A series of dissolution and characterization studies has been performed to determine if FB-Line residues stored in desicooler containers will dissolve using a modified H-Canyon processing flowsheet. Samples of desicooler materials were used to evaluate dissolving characteristics in the low-molar nitric acid solutions used in H-Canyon dissolvers. The selection for the H-Canyon dissolution of desicooler residues was based on their high-enriched uranium content and trace levels of plutonium. Test results showed that almost all of the enriched uranium will dissolve from the desicooler materials after extended boiling in one molar nitric acid solutions. The residue that contained uranium after completion of the extended boiling cycle consisted of brown solids that had agglomerated into large pieces and were floating on top of the dissolver solution. Addition of tenth molar fluoride to a three molar nitric acid solution containing boron did not dissolve remaining uranium from the brown solids. Only after boiling in an eight molar nitric acid-tenth molar fluoride solution without boron did remaining uranium and aluminum dissolve from the brown solids. The amount of uranium associated with brown solids would be approximately 1.4 percent of the total uranium content of the desicooler materials. The brown solids that remain in the First Uranium Cycle feed will accumulate at the organic/aqueous interface during solvent extraction operations. Most of the undissolved white residue that remained after extended boiling was aluminum oxide containing additional trace quantities of impurities. However, the presence of mercury used in H-Canyon dissolvers should complete the dissolution of these aluminum compounds.

Gray, J.H.

2003-06-23T23:59:59.000Z

133

Design, Synthesis and Evaluation of Liquid-like Nanoparticle Organic Hybrid Materials for Carbon Dioxide Capture.  

E-Print Network [OSTI]

??Given the rapid increase in atmospheric concentration of CO2, the development of efficient CO2 capture technologies is critical for the future of carbon-based energy. Currently,… (more)

Lin, Kun-Yi

2012-01-01T23:59:59.000Z

134

A New Organic Acid to Stimulate Deep Wells in Carbonate Reservoirs  

E-Print Network [OSTI]

Carbonate acidizing has been carried out using HCl-based stimulation fluids for decades. However, at high temperatures, HCl does not produce acceptable results because of its fast reaction, acid penetration, and hence surface dissolution, and its...

Al-Douri, Ahmad F

2014-05-28T23:59:59.000Z

135

Changes in soil organic carbon storage predicted by Earth system models during the 21st century  

E-Print Network [OSTI]

carbon changes in Earth system models K. E. O. Todd-Brown etcarbon changes in Earth system models K. E. O. Todd-Brown etcarbon changes in Earth system models K. E. O. Todd-Brown et

2013-01-01T23:59:59.000Z

136

Free Zinc Ion and Dissolved Orthophosphate Effects on  

E-Print Network [OSTI]

historic heavy-metal mining and smelting areas. The lake transitions longitudinally from mesotrophic toxic response by phytoplankton and higher- trophic-level organisms due to elevated dissolved-metal of nutrients, toxicants, and sediment from two major riverine inputs; the St. Joe River from the south

137

Electrodeposited Manganese Oxides on Three-Dimensional Carbon Nanotube Substrate: Supercapacitive Behaviour in Aqueous and Organic Electrolytes  

SciTech Connect (OSTI)

Thin amorphous manganese oxide layers with a thickness of 3-5nm are electrodeposited on a carbon nanotube (CNT) film substrate that has a three-dimensional nanoporous structure (denoted asMnO2/CNT electrode). For the purpose of comparison, manganese oxide films are also electrodeposited on a flat Pt-coated Si wafer substrate (denoted as MnO2 film electrode). The pseudocapacitive properties of the MnO2 film and MnO2/CNT electrodes are examined in both aqueous electrolyte (1.0M KCl) and nonaqueousorganic electrolyte (1.0M LiClO4 in propylene carbonate). While both types of electrode showpseudocapacitive behaviour in the aqueous electrolyte, only the MnO2/CNT electrode does so in the organic electrolyte, due to its high oxide/electrolyte interfacial area and improved electron conduction through the CNT substrate. Compared with the MnO2 film electrode, the MnO2/CNT electrode shows a much higher specific capacitance and better high-rate capability, regardless of the electrolyte used.Use of the organic electrolyte results in a ?6 times higher specific energy compared with that obtained with the aqueous electrolyte, while maintaining a similar specific power. The construction of a threedimensional nanoporous network structure consisting of a thin oxide layer on a CNT film substrate at the nm scale and the use of an organic electrolyte are promising approaches to improving the specific energyof supercapacitors.

Nam,K.W.; Yang,X.

2009-03-01T23:59:59.000Z

138

Carbon oxidation state as a metric for describing the chemistry of atmospheric organic aerosol  

E-Print Network [OSTI]

A detailed understanding of the sources, transformations and fates of organic species in the environment is crucial because of the central roles that they play in human health, biogeochemical cycles and the Earth's climate. ...

Kroll, Jesse

139

Final Technical Report: Ocean CO{sub 2} Measurements for the WOCE Hydrographic Survey in the Pacific Ocean, 1992-1995 Field Years: Shore Based Analysis of Dissolved Inorganic Carbon January 1, 1993-April 15, 1998  

SciTech Connect (OSTI)

Participation in the hydrographic survey of the world ocean circulation experiment (WOCE) began in December 1990 with a two year grant from DOE for shore related analyses of inorganic carbon in sea water. These analyses were intended to assure that the measurements carried out under difficult laboratory conditions on board ships were consistent with measurements made under more carefully controlled shore laboratory conditions.

Keeling, Charles D.

1998-04-15T23:59:59.000Z

140

DISSOLVED CONCENTRATION LIMITS OF RADIOACTIVE ELEMENTS  

SciTech Connect (OSTI)

The purpose of this study is to evaluate dissolved concentration limits (also referred to as solubility limits) of elements with radioactive isotopes under probable repository conditions, based on geochemical modeling calculations using geochemical modeling tools, thermodynamic databases, field measurements, and laboratory experiments. The scope of this activity is to predict dissolved concentrations or solubility limits for elements with radioactive isotopes (actinium, americium, carbon, cesium, iodine, lead, neptunium, plutonium, protactinium, radium, strontium, technetium, thorium, and uranium) relevant to calculated dose. Model outputs for uranium, plutonium, neptunium, thorium, americium, and protactinium are provided in the form of tabulated functions with pH and log fCO{sub 2} as independent variables, plus one or more uncertainty terms. The solubility limits for the remaining elements are either in the form of distributions or single values. Even though selection of an appropriate set of radionuclides documented in Radionuclide Screening (BSC 2002 [DIRS 160059]) includes actinium, transport of Ac is not modeled in the total system performance assessment for the license application (TSPA-LA) model because of its extremely short half-life. Actinium dose is calculated in the TSPA-LA by assuming secular equilibrium with {sup 231}Pa (Section 6.10); therefore, Ac is not analyzed in this report. The output data from this report are fundamental inputs for TSPA-LA used to determine the estimated release of these elements from waste packages and the engineered barrier system. Consistent modeling approaches and environmental conditions were used to develop solubility models for the actinides discussed in this report. These models cover broad ranges of environmental conditions so they are applicable to both waste packages and the invert. Uncertainties from thermodynamic data, water chemistry, temperature variation, and activity coefficients have been quantified or otherwise addressed.

P. Bernot

2005-07-13T23:59:59.000Z

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


141

Organic carbon aerogels from the sol-gel polymerization of phenolic-furfural mixtures  

DOE Patents [OSTI]

The sol-gel polymerization of a phenolic-furfural mixture in dilute solution leads to a highly cross-linked network that can be supercritically dried to form a high surface area foam. These porous materials have cell/pore sizes {<=}1000 {angstrom}, and although they are dark brown in color, they can be classified as a new type of aerogel. The phenolic-furfural aerogel can be pyrolyzed in an inert atmosphere at 1050 C to produce carbon aerogels. This new aerogel may be used for thermal insulation, chromatographic packing, water filtration, ion-exchange, and carbon electrodes for energy storage devices, such as batteries and double-layer capacitors. 8 figs.

Pekala, R.W.

1998-04-28T23:59:59.000Z

142

Organic carbon aerogels from the sol-gel polymerization of phenolic-furfural mixtures  

DOE Patents [OSTI]

The sol-gel polymerization of a phenolic-furfural mixture in dilute solution leads to a highly cross-linked network that can be supercritically dried to form a high surface area foam. These porous materials have cell/pore sizes .ltoreq.1000 .ANG., and although they are dark brown in color, they can be classified as a new type of aerogel. The phenolic-furfural aerogel can be pyrolyzed in an inert atmosphere at 1050.degree. C. to produce carbon aerogels. This new aerogel may be used for thermal insulation, chromatographic packing, water filtration, ion-exchange, and carbon electrodes for energy storage devices, such as batteries and double-layer capacitors.

Pekala, Richard W. (Pleasant Hill, CA)

1998-04-28T23:59:59.000Z

143

Carbon tetrachloride contamination, 200 West Area, Hanford Site: Arid Site Integrated Demonstration for remediation of volatile organic compounds  

SciTech Connect (OSTI)

The Arid State Integrated Demonstration is a US Department of Energy (DOE) program targeted at the acquisition, development, demonstration, and deployment of technologies for evaluation and cleanup of volatile organic and associated contaminants in soils and ground waters. Several DOE laboratories, universities, and industry will participate in the program. Candidate technologies will be demonstrated in the areas of site characterization; performance prediction, monitoring, and evaluations; contaminant extraction and ex situ treatment; in situ remediations; and site closure and monitoring. The performance of these demonstrated technologies will be compared to baseline technologies and documented to promote the transfer of new technologies to industry for use at DOE facilities. The initial host site is the Hanford Site's 200 West Area. The location of the demonstration contains primarily carbon tetrachloride (CCl{sub 4}), chloroform, and a variety of associated mixed waste contaminants. Chemical processes used to recover and purify plutonium at Hanford's plutonium finishing plant (Z Plant) resulted in the production of actinide-bearing waste liquid. Both aqueous and organic liquid wastes were generated, and were routinely discharged to subsurface disposal facilities. The primary radionuclide in the waste streams was plutonium, and the primary organic was CCl{sub 4}. This paper contains brief descriptions of the principal CCl{sub 4} waste disposal facilities in Hanford's 200 West Area, associated hydrogeology, existing information on the extent of soil and ground-water contamination, and a conceptual outline of suspected subsurface CCl{sub 4} distributions.

Last, G.V. (Pacific Northwest Lab., Richland, WA (United States)); Rohay, V.J. (Westinghouse Hanford Co., Richland, WA (United States))

1991-05-06T23:59:59.000Z

144

Carbon tetrachloride contamination, 200 West Area, Hanford Site: Arid Site Integrated Demonstration for remediation of volatile organic compounds  

SciTech Connect (OSTI)

The Arid State Integrated Demonstration is a US Department of Energy (DOE) program targeted at the acquisition, development, demonstration, and deployment of technologies for evaluation and cleanup of volatile organic and associated contaminants in soils and ground waters. Several DOE laboratories, universities, and industry will participate in the program. Candidate technologies will be demonstrated in the areas of site characterization; performance prediction, monitoring, and evaluations; contaminant extraction and ex situ treatment; in situ remediations; and site closure and monitoring. The performance of these demonstrated technologies will be compared to baseline technologies and documented to promote the transfer of new technologies to industry for use at DOE facilities. The initial host site is the Hanford Site`s 200 West Area. The location of the demonstration contains primarily carbon tetrachloride (CCl{sub 4}), chloroform, and a variety of associated mixed waste contaminants. Chemical processes used to recover and purify plutonium at Hanford`s plutonium finishing plant (Z Plant) resulted in the production of actinide-bearing waste liquid. Both aqueous and organic liquid wastes were generated, and were routinely discharged to subsurface disposal facilities. The primary radionuclide in the waste streams was plutonium, and the primary organic was CCl{sub 4}. This paper contains brief descriptions of the principal CCl{sub 4} waste disposal facilities in Hanford`s 200 West Area, associated hydrogeology, existing information on the extent of soil and ground-water contamination, and a conceptual outline of suspected subsurface CCl{sub 4} distributions.

Last, G.V. [Pacific Northwest Lab., Richland, WA (United States); Rohay, V.J. [Westinghouse Hanford Co., Richland, WA (United States)

1991-05-06T23:59:59.000Z

145

Extraction of semivolatile organic compounds from high-efficiency particulate air (HEPA) filters by supercritical carbon dioxide  

SciTech Connect (OSTI)

Supercritical fluid extraction (SFE) using unmodified carbon dioxide has been explored as an alternative method for the extraction of semivolatile organic compounds from high-efficiency particulate air (HEPA) filters. HEPA filters provide the final stage of containment on many exhaust systems in US Department of Energy (DOE) facilities by preventing the escape of chemical and radioactive materials entrained in the exhausted air. The efficiency of the filters is tested by the manufacturer and DOE using dioctylphthalate (DOP), a substance regulated by the US Environmental Protection Agency under the Resource Conservation and Recovery Act. Therefore, the filters must be analyzed for semivolatile organics before disposal. Ninety-eight acid, base, and neutral semivolatile organics were spiked onto blank HEPA material and extracted using SFE, Soxhlet, automated Soxhlet, and sonication techniques. The SFE conditions were optimized using a Dionex SFE-703 instrument. Average recoveries for the 98 semivolatile compounds are 82.7% for Soxhlet, 74.0% for sonication, 70.2% for SFE, and 62.9% for Soxtec. Supercritical fluid extraction reduces the extraction solvent volume to 10--15 mL, a factor of 20--30 less than Soxhlet and more than 5 times less than Soxtec and sonication. Extraction times of 30--45 min are used compared to 16--18 h for Soxhlet extraction.

Schilling, J.B.

1997-09-01T23:59:59.000Z

146

Effect of an organic molecular coating on control over the conductance of carbon nanotube channel  

SciTech Connect (OSTI)

It is shown that the coating of carbon nanotubes with molecules with a constant dipole moment changes the conductance of the tubes due to a variation in the structure of energy levels that participate in charge transport. The I–V characteristics of the investigated structures exhibit significant dependence of the channel conductance on the gate potential. The observed memory effect of conductance level can be explained by the rearrangement of polar groups and molecules as a whole in an electric field. The higher the dipole moment per unit length and the weaker the intermolecular interaction, the faster the rearrangement process is.

Bobrinetskiy, I. I.; Emelianov, A. V.; Nevolin, V. K., E-mail: vkn@miee.ru; Romashkin, A. V. [National Research University “Moscow Institute of Electronic Technology” (MIET) (Russian Federation)

2014-12-15T23:59:59.000Z

147

TREATMENT OF HYDROCARBON, ORGANIC RESIDUE AND PRODUCTION CHEMICAL DAMAGE MECHANISMS THROUGH THE APPLICATION OF CARBON DIOXIDE IN NATURAL GAS STORAGE WELLS  

SciTech Connect (OSTI)

Core specimens and several material samples were collected from two natural gas storage reservoirs. Laboratory studies were performed to characterize the samples that were believed to be representative of a reservoir damage mechanism previously identified as arising from the presence of hydrocarbons, organic residues or production chemicals. A series of laboratory experiments were performed to identify the sample materials, use these materials to damage the flow capacity of the core specimens and then attempt to remove or reduce the induced damage using either carbon dioxide or a mixture of carbon dioxide and other chemicals. Results of the experiments showed that pure carbon dioxide was effective in restoring flow capacity to the core specimens in several different settings. However, in settings involving asphaltines as the damage mechanism, both pure carbon dioxide and mixtures of carbon dioxide and other chemicals provided little effectiveness in damage removal.

Lawrence J. Pekot; Ron Himes

2004-05-31T23:59:59.000Z

148

Large Magnetization at Carbon Surfaces  

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

Large Magnetization at Carbon Surfaces Large Magnetization at Carbon Surfaces Print Wednesday, 31 August 2011 00:00 From organic matter to pencil lead, carbon is a versatile...

149

Organization  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary)morphinanInformation Desert Southwest Regionat CornellInternships,(SC) Laboratories »OrganicOrganization

150

Cold Dissolved Saltcake Waste Simulant Development, Preparation, and Analysis  

SciTech Connect (OSTI)

CH2M HILL Hanford Group, Inc. is identifying and developing supplemental process technologies to accelerate the Hanford tank waste cleanup mission. Bulk vitrification, containerized grout, and steam reforming are three technologies under consideration for treatment of the radioactive saltcake wastes in 68 single-shell tanks. To support development and testing of these technologies, Pacific Northwest National Laboratory (PNNL) was tasked with developing a cold dissolved saltcake simulant formulation to be representative of an actual saltcake waste stream, preparing 25- and 100-L batches of the simulant, and analyzing the composition of the batches to ensure conformance to formulation targets. Lacking a defined composition for dissolved actual saltcake waste, PNNL used available tank waste composition information and an equilibrium chemistry model (Environmental Simulation Program [ESP{trademark}]) to predict the concentrations of analytes in solution. Observations of insoluble solids in initial laboratory preparations for the model-predicted formulation prompted reductions in the concentration of phosphate and silicon in the final simulant formulation. The analytical results for the 25- and 100-L simulant batches, prepared by an outside vendor to PNNL specifications, agree within the expected measurement accuracy ({approx}10%) of the target concentrations and are highly consistent for replicate measurements, with a few minor exceptions. In parallel with the production of the 2nd simulant batch (100-L), a 1-L laboratory control sample of the same formulation was carefully prepared at PNNL to serve as an analytical standard. The instrumental analyses indicate that the vendor prepared batches of solution adequately reflect the as-formulated simulant composition. In parallel with the simulant development effort, a nominal 5-M (molar) sodium actual waste solution was prepared at the Hanford Site from a limited number of tank waste samples. Because this actual waste solution w as also to be used for testing the supplemental treatment technologies, the modeled simulant formulation was predicated on the composite of waste samples used to prepare it. Subsequently, the actual waste solution was filtered and pretreated to remove radioactive cesium at PNNL and then analyzed using the same instrumentation and procedures applied to the simulant samples. The overall agreement of measured simulant and actual waste solution compositions is better than {+-}10% for the most concentrated species including sodium, nitrate, hydroxide, carbonate, and nitrite. While the magnitude of the relative difference in the simulant and actual waste composition is large (>20% difference) for a few analytes (aluminum, chromium, fluoride, potassium, and total organic carbon), the absolute differences in concentration are in general not appreciable. Our evaluation is that these differences in simulant and actual waste solutions should have a negligible impact on bulk vitrification and containerized grout process testing, while the impact of the low aluminum concentration on steam reforming is yet to be determined.

Rassat, Scot D.; Mahoney, Lenna A.; Russell, Renee L.; Bryan, Samuel A.; Sell, Rachel L.

2003-05-13T23:59:59.000Z

151

Classification of Multiple Types of Organic Carbon Composition in Atmospheric Particles by Scanning Transmission X-Ray Microscopy Analysis  

SciTech Connect (OSTI)

A scanning transmission X-ray microscope at the Lawrence Berkeley National Laboratory is used to measure organic functional group abundance and morphology of atmospheric aerosols. We present a summary of spectra, sizes, and shapes observed in 595 particles that were collected and analyzed between 2000 and 2006. These particles ranged between 0.1 and 12 mm and represent aerosols found in a large range of geographical areas, altitudes, and times. They include samples from seven different field campaigns: PELTI, ACE-ASIA, DYCOMS II, Princeton, MILAGRO (urban), MILAGRO (C-130), and INTEX-B. At least 14 different classes of organic particles show different types of spectroscopic signatures. Different particle types are found within the same region while the same particle types are also found in different geographical domains. Particles chemically resembling black carbon, humic-like aerosols, pine ultisol, and secondary or processed aerosol have been identified from functional group abundance and comparison of spectra with those published in the literature.

Kilcoyne, Arthur L; Takahama, S.; Gilardoni, S.; Russell, L.M.; Kilcoyne, A.L.D.

2007-05-16T23:59:59.000Z

152

Designer organisms for photosynthetic production of ethanol from carbon dioxide and water  

DOE Patents [OSTI]

The present invention provides a revolutionary photosynthetic ethanol production technology based on designer transgenic plants, algae, or plant cells. The designer plants, designer algae, and designer plant cells are created such that the endogenous photosynthesis regulation mechanism is tamed, and the reducing power (NADPH) and energy (ATP) acquired from the photosynthetic water splitting and proton gradient-coupled electron transport process are used for immediate synthesis of ethanol (CH.sub.3CH.sub.2OH) directly from carbon dioxide (CO.sub.2) and water (H.sub.2O). The ethanol production methods of the present invention completely eliminate the problem of recalcitrant lignocellulosics by bypassing the bottleneck problem of the biomass technology. The photosynthetic ethanol-production technology of the present invention is expected to have a much higher solar-to-ethanol energy-conversion efficiency than the current technology and could also help protect the Earth's environment from the dangerous accumulation of CO.sub.2 in the atmosphere.

Lee, James Weifu (Knoxville, TN)

2011-07-05T23:59:59.000Z

153

{sup 210}Pb dating of sediments from the central and northern Adriatic Sea: deposition and preservation of sedimentary organic carbon  

SciTech Connect (OSTI)

Lead-210 ({sup 21O}Pb) and organic C depth distribution profiles in sediments from the northern and central Adriatic Sea were measured as part of the EEC funded project on Eutrophic Limits of the Northern Adriatic (ELNA). {sup 210}Pb derived mass-accumulation rates decrease southward from between 0.15 and 0.2 g cm{sup -2}y{sup -1} close to the Po River outflow (> 24 m, water depth) to less than 0.04 g cm{sup -2}y{sup -1} in the Jabuka Pit (246 m, water depth) in the central Adriatic Sea. The mass- accumulation rates obtained in the Jabuka Pit correspond to mean sedimentation rates of about 0.03 cm y{sup -1} (ref. porosity = 0.5) and fall between 5 to 20 times lower than rates found for north Adriatic shelf cores. Estimated sedimentation rates are considered as upper limits because of the possible effects of bioturbation and physical disturbance on the {sup 21O}Pb sedimentary record but are consistent with data from previous work. Rates of sediment accumulation and carbon burial appear to be strongly influenced by the transport of fluvial materials from land and transport of fine-grained particles. First-order estimates of organic C burial rates into surface sediment ranged from 1 to 0.028 mMol cm{sup -2}y{sup -1} between the Po delta and the Jabuka Pit regions, respectively. We estimate that a maximum of 50% of organic C preserved in surface sediment may be derived from biological production in the overlying water column.

Hamilton, T. F., LLNL

1998-04-01T23:59:59.000Z

154

Carbon Dioxide Removal from Flue Gas Using Microporous Metal Organic Frameworks  

SciTech Connect (OSTI)

UOP LLC, a Honeywell Company, in collaboration with Professor Douglas LeVan at Vanderbilt University (VU), Professor Adam Matzger at the University of Michigan (UM), Professor Randall Snurr at Northwestern University (NU), and Professor Stefano Brandani at the University of Edinburgh (UE), supported by Honeywell's Specialty Materials business unit and the Electric Power Research Institute (EPRI), have completed a three-year project to develop novel microporous metal organic frameworks (MOFs) and an associated vacuum-pressure swing adsorption (vPSA) process for the removal of CO{sub 2} from coal-fired power plant flue gas. The project leveraged the team's complementary capabilities: UOP's experience in materials development and manufacturing, adsorption process design and process commercialization; LeVan and Brandani's expertise in high-quality adsorption measurements; Matzger's experience in syntheis of MOFs and the organic components associated with MOFs; Snurr's expertise in molecular and other modeling; Honeywell's expertise in the manufacture of organic chemicals; and, EPRI's knowledge of power-generation technology and markets. The project was successful in that a selective CO{sub 2} adsorbent with good thermal stability and reasonable contaminant tolerance was discovered, and a low cost process for flue gas CO{sub 2} capture process ready to be evaluated further at the pilot scale was proposed. The team made significant progress toward the current DOE post-combustion research targets, as defined in a recent FOA issued by NETL: 90% CO{sub 2} removal with no more than a 35% increase in COE. The team discovered that favorable CO{sub 2} adsorption at more realistic flue gas conditions is dominated by one particular MOF structure type, M/DOBDC, where M designates Zn, Co, Ni, or Mg and DOBDC refers to the form of the organic linker in the resultant MOF structure, dioxybenzenedicarboxylate. The structure of the M/DOBDC MOFs consists of infinite-rod secondary building units bound by DOBDC resulting in 1D hexagonal pores about 11 angstroms in diameter. Surface areas range from 800 to 1500 sq m/g for the different MOFs. Mg/DOBDC outperformed all MOF and zeolite materials evaluated to date, with about 25 wt% CO{sub 2} captured by this MOF at flue gas conditions ({approx}0.13 atm CO{sub 2} pressure, 311K). In simulated flue gas without oxygen, the zero-length (ZLC) system was very useful in quickly simulating the effect of long term exposure to impurities on the MOFs. Detailed adsorption studies on MOF pellets have shown that water does not inhibit CO{sub 2} adsorption for MOFs as much as it does for typical zeolites. Moreover, some MOFs retain a substantial CO{sub 2} capacity even with a modest water loading at room temperature. Molecular modeling was a key activity in three areas of our earlier DOE/NETL-sponsored MOF-based research on CC. First, the team was able to effectively simulate CO{sub 2} and other gas adsorption isotherms for more than 20 MOFs, and the knowledge obtained was used to help predict new MOF structures that should be effective for CO{sub 2} adsorption at low pressure. The team also showed that molecular modeling could be utilized to predict the hydrothermal stability of a given MOF. Finally, the team showed that low moisture level exposure actually enhanced the CO{sub 2} adsorption performance of a particular MOF, HKUST-1.

David A Lesch

2010-06-30T23:59:59.000Z

155

Method of separating lignocellulosic material into lignin, cellulose and dissolved sugars  

DOE Patents [OSTI]

A method is described for separating lignocellulosic material into (a) lignin, (b) cellulose, and (c) hemicellulose and dissolved sugars. Wood or herbaceous biomass is digested at elevated temperature in a single-phase mixture of alcohol, water and a water-immiscible organic solvent (e.g., a ketone). After digestion, the amount of water or organic solvent is adjusted so that there is phase separation. The lignin is present in the organic solvent, the cellulose is present in a solid pulp phase, and the aqueous phase includes hemicellulose and any dissolved sugars.

Black, S.K.; Hames, B.R.; Myers, M.D.

1998-03-24T23:59:59.000Z

156

Method of separating lignocellulosic material into lignin, cellulose and dissolved sugars  

DOE Patents [OSTI]

A method for separating lignocellulosic material into (a) lignin, (b) cellulose, and (c) hemicellulose and dissolved sugars. Wood or herbaceous biomass is digested at elevated temperature in a single-phase mixture of alcohol, water and a water-immiscible organic solvent (e.g., a ketone). After digestion, the amount of water or organic solvent is adjusted so that there is phase separation. The lignin is present in the organic solvent, the cellulose is present in a solid pulp phase, and the aqueous phase includes hemicellulose and any dissolved sugars.

Black, Stuart K. (Denver, CO); Hames, Bonnie R. (Westminster, CO); Myers, Michele D. (Dacono, CO)

1998-01-01T23:59:59.000Z

157

Emission and Chemistry of Organic Carbon in the Gas and Aerosol Phase at a Sub-Urban Site Near Mexico City in March 2006 During the MILAGRO Study  

SciTech Connect (OSTI)

Volatile organic compounds (VOCs) and carbonaceous aerosol were measured at a sub-urban site near Mexico City in March of 2006 during the MILAGRO study (Megacity Initiative: Local and Global Research Objectives). Diurnal variations of hydrocarbons, elemental carbon (EC) and hydrocarbon-like organic aerosol (HOA) were dominated by a high peak in the early morning when local emissions accumulated in a shallow boundary layer, and a minimum in the afternoon when the emissions were diluted in a significantly expanded boundary layer and, in case of the reactive gases, removed by OH. In comparison, diurnal variations of species with secondary sources such as the aldehydes, ketones, oxygenated organic aerosol (OOA) and water-soluble organic carbon (WSOC) stayed relatively high in the afternoon indicating strong photochemical formation. Emission ratios of many hydrocarbon species relative to CO were higher in Mexico City than in the U.S., but we found similar emission ratios for most oxygenated VOCs and organic aerosol. Secondary formation of acetone may be more efficient in Mexico City than in the U.S., due to higher emissions of alkane precursors from the use of liquefied petroleum gas. Secondary formation of organic aerosol was similar between Mexico City and the U.S. Combining the data for all measured gas and aerosol species, we describe the budget of total observed organic carbon (TOOC), and find that the enhancement ratio of TOOC relative to CO is conserved between the early morning and mid afternoon despite large compositional changes. Finally, the influence of biomass burning is investigated using the measurements of acetonitrile, which was found to correlate with levoglucosan in the particle phase. Diurnal variations of acetonitrile indicate a contribution from local burning sources. Scatter plots of acetonitrile versus CO suggest that the contribution of biomass burning to the enhancement of most gas and aerosol species was not dominant and perhaps not dissimilar from observations in the U.S.

de Gouw, Joost A.; Welsh-Bon, Daniel; Warneke, Carsten; Kuster, W. C.; Alexander, M. L.; Baker, Angela K.; Beyersdorf, Andreas J.; Blake, D. R.; Canagaratna, Manjula R.; Celada, A. T.; Huey, L. G.; Junkermann, W.; Onasch, Timothy B.; Salcido, A.; Sjostedt, S. J.; Sullivan, Amy; Tanner, David J.; Vargas-Ortiz, Leroy; Weber, R. J.; Worsnop, Douglas R.; Yu, Xiao-Ying; Zaveri, Rahul A.

2009-05-28T23:59:59.000Z

158

Dissolved aluminum in the Gulf of Mexico  

E-Print Network [OSTI]

in areas of minimum sediment resuspension. With limited data available it appears that the boundary of the sediment/water interface does release dissolved Al, but kinetically Al should decrease with depth in the sediment during authigenesis. The Al... DISSOLVED ALUMINUM IN THE GULF OF MEXICO A Thesis by PEGGY LYNNE MYRE Submitted to the Office of Graduate Studies of Texas A6M University in partial fulfillment of the requirements for the degree of MASTER OF SCIENCE August 1990 Majo...

Myre, Peggy Lynne

1990-01-01T23:59:59.000Z

159

Molecular Structure and Stability of Dissolved Lithium Polysulfide...  

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

Stability of Dissolved Lithium Polysulfide Species. Molecular Structure and Stability of Dissolved Lithium Polysulfide Species. Abstract: Ability to predict the solubility and...

160

On carbon footprints and growing energy use  

E-Print Network [OSTI]

On carbon footprints and growing energy use Curtis M.reductions in the carbon footprint of a growing organizationhis own organization's carbon footprint and answers this

Oldenburg, C.M.

2012-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


161

Impacts of engineering nanoparticles on dissolved organic matter assembly  

E-Print Network [OSTI]

One of promising geoengineering solutions, ocean gardening (is one of potential geoengineering approaches (Figueroa et

Chen, Chi-Shuo

2012-01-01T23:59:59.000Z

162

Nature and Transformation of Dissolved Organic Matter in  

E-Print Network [OSTI]

influence on transformations that occur during treatment, (ii) the climate factors have a secondary effect. As wastewater treatment plant effluent passes through treatment wetlands, the DOM undergoes transformation selected to evaluate the effects of climate, wastewater characteristics, and operating conditions

163

Photolytic processing of secondary organic aerosols dissolved in cloud  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear Security Administration the1 - September 2006 TheStevenAdministration

164

Carbon dioxide-assisted fabrication of highly uniform submicron-sized colloidal carbon spheres via hydrothermal carbonization using soft drink  

SciTech Connect (OSTI)

An eco-friendly and economical method for the formation of uniform-sized carbon spheres by hydrothermal dehydration/condensation of a commercial carbonated beverage at 200 oC is reported. CO2 dissolved in the beverage accelerates the dehydration kinetics of the dissolved sugar molecules leading to production of homogeneous carbon spheres having a diameter less than 850 nm. In the presence of CO2, the rough surface of these carbon spheres likely results from continuous Ostwald ripening of constituent microscopic carbon-containing spheres that are formed by subsequent polymerization of intermediate HMF molecules.

Moon, Gun-Hee; Shin, Yongsoon; Arey, Bruce W.; Wang, Chong M.; Exarhos, Gregory J.; Choi, Wonyong; Liu, Jun

2012-10-01T23:59:59.000Z

165

Barium in Twilight Zone suspended matter as a potential proxy for particulate organic carbon remineralization: Results for the North Pacific  

E-Print Network [OSTI]

considering TdR conversion factors 1 and 2 x 10 18 cellsrates using TdR conversion factors of 1 - 2 x 10 18mol -1 and a carbon conversion factor of 15 fg C cell -1 ;

Dehairs, F.

2008-01-01T23:59:59.000Z

166

Synthesis of Amine-Modified Aerogel Sorbents and Metal-Organic Framework-5 (MOF-5) Membranes for Carbon Dioxide Separation.  

E-Print Network [OSTI]

??Amine-modified solid sorbents and membrane separation are promising technologies for separation and capture of carbon dioxide (CO2) from combustion flue gas. Amine absorption processes are… (more)

Rosa, Teresa M.

2010-01-01T23:59:59.000Z

167

Simulation of a continuous rotary dissolver  

SciTech Connect (OSTI)

This paper describes the simulation of a rotating, multistage chemical reactor that dissolves spent nuclear fuel for reprocessing in a breeder cycle. The continuous, time-dependent process model of a dissolver was developed using the Advanced Continuous Simulation Language (ACSL) to calculate various temperatures and the masses of the chemical constituents of the solution in each stage. The Gear integration algorithm (Gear 1971) was used to accommodate the stiff dynamics. An arrangement of interacting discrete sections was employed to cause fresh fuel to be added and dissolver rotations to occur at appropriate times. By changing various constants, the model can simulate the effect of different fuel compositions and operational scenarios. The model code is a valuable tool for analysis of the performance of the dissolution system and has been instrumental in its design. 5 refs., 7 figs.

Carnal, C.L.; Hardy, J.E.; Lewis, B.E.

1989-01-01T23:59:59.000Z

168

Absorption Properties of Dissolved and Particulate Matter in Turbid Productive Inland Lakes  

E-Print Network [OSTI]

of solar energy: colored dissolved organic matter (subscript CDOM), suspended non-algal particles of North America (Nebraska, USA). STUDY AREA Data were collected in eastern Nebraska during 2002 and 2003 as freshwater supplies and recreational areas. Optical properties of lakes may provide for example the time

Gitelson, Anatoly

169

Methylation of Mercury by Bacteria Exposed to Dissolved, Nanoparticulate, and Microparticulate Mercuric Sulfides  

E-Print Network [OSTI]

Methylation of Mercury by Bacteria Exposed to Dissolved, Nanoparticulate, and Microparticulate in the environment is partly controlled by the bioavailability of inorganic divalent mercury (Hg(II)) to anaerobic matter to form chemical species that include organic-coated mercury sulfide nanoparticles as reaction

170

Widespread influence of resuspended sediments on oceanic particulate organic carbon: Insights from radiocarbon and aluminum contents in sinking particles  

E-Print Network [OSTI]

between proxy records in a sediment drift, Science, 298,the Japan Sea measured with sediment traps, Mar. Chem. , 91,and organic constituents in sediments from the con- tinental

Hwang, Jeomshik; Druffel, Ellen R. M; Eglinton, Timothy I

2010-01-01T23:59:59.000Z

171

Preservation of iron(II) by carbon-rich matrices in a hydrothermal plume  

SciTech Connect (OSTI)

Hydrothermal venting associated with mid-ocean ridge volcanism is globally widespread. This venting is responsible for a dissolved iron flux to the ocean that is approximately equal to that associated with continental riverine runoff. For hydrothermal fluxes, it has long been assumed that most of the iron entering the oceans is precipitated in inorganic forms. However, the possibility of globally significant fluxes of iron escaping these mass precipitation events and entering open-ocean cycles is now being debated, and two recent studies suggest that dissolved organic ligands might influence the fate of hydrothermally vented metals. Here we present spectromicroscopic measurements of iron and carbon in hydrothermal plume particles at the East Pacific Rise mid-ocean ridge. We show that organic carbon-rich matrices, containing evenly dispersed iron(II)-rich materials, are pervasive in hydrothermal plume particles. The absence of discrete iron(II) particles suggests that the carbon and iron associate through sorption or complexation. We suggest that these carbon matrices stabilize iron(II) released from hydrothermal vents in the region, preventing its oxidation and/or precipitation as insoluble minerals. Our findings have implications for deep-sea biogeochemical cycling of iron, a widely recognized limiting nutrient in the oceans.

Toner, Brandy M.; Fakra, Sirine C.; Manganini, Steven J.; Santelli, Cara M.; Marcus, Matthew A.; Moffett, James W.; Rouxel, Olivier; German, Christopher R.; Edwards, Katrina J.

2008-09-20T23:59:59.000Z

172

Thermodynamics and kinetics of hydrophobic organic compound sorption in natural sorbents and quantification of black carbon by electron microscopy  

E-Print Network [OSTI]

The sorption behaviors of hydrophobic organic compounds (HOCs) in sediments were investigated using pyrene. Native pyrene desorbed slowly, taking from weeks to months to equilibrate. The end-point data suggested that, at ...

Kuo, Dave Ta Fu, 1978-

2010-01-01T23:59:59.000Z

173

Carbon dioxide fixation by Metallosphaera yellowstonensis and acidothermophilic iron-oxidizing microbial communities from Yellowstone National Park  

SciTech Connect (OSTI)

The fixation of inorganic carbon (as carbon dioxide) has been documented in all three domains of life and results in the biosynthesis of a diverse suite of organic compounds that support the growth of heterotrophic organisms. The primary aim of this study was to assess the importance of carbon dioxide fixation in high-temperature Fe(III)-oxide mat communities and in pure cultures of one of the dominant Fe(II)-oxidizing organisms (Metallosphaera yellowstonensis strain MK1) present in situ. Protein-encoding genes of the complete 3-hydroxypropionate/4-hydroxybutyrate (3-HP/4-HB) carbon fixation pathway were identified in pure-cultures of M. yellowstonensis strain MK1. Metagenome sequencing from the same environments also revealed genes for the 3-HP/4-HB pathway belonging to M. yellowstonensis populations, as well as genes for a complete reductive TCA cycle from Hydrogenobaculum spp. (Aquificales). Stable isotope (13CO2) labeling was used to measure the fixation of CO2 by M. yellowstonensis strain MK1, and in ex situ assays containing live Fe(III)-oxide microbial mats. Results showed that M. yellowstonensis strain MK1 fixes CO2 via the 3-HP/4-HB pathway with a fractionation factor of ~ 2.5 ‰. Direct analysis of the 13C composition of dissolved inorganic C (DIC), dissolved organic C (DOC), landscape C and microbial mat C showed that mat C is comprised of both DIC and non-DIC sources. The estimated contribution of DIC carbon to biomass C (> ~ 35%) is reasonably consistent with the relative abundance of known chemolithoautotrophs and corresponding CO2 fixation pathways detected in metagenome sequence. The significance of DIC as a major source of carbon for Fe-oxide mat communities provides a foundation for examining microbial interactions in these systems that are dependent on the activity of autotrophic organisms such as Hydrogenobaculum and Metallosphaera spp.

Jennings, Ryan; Whitmore, Laura M.; Moran, James J.; Kreuzer, Helen W.; Inskeep, William P.

2014-05-01T23:59:59.000Z

174

atmospheric organic matter: Topics by E-print Network  

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

Theses and Dissertations Summary: ??Dissolved natural organic matter (NOM) and heavy metals are ubiquitous in aqueous and terrestrial systems. Adsorption processes involving...

175

IMPROVEMENTS IN MODELLING DISSOLVED OXYGEN IN ACTIVATED SLUDGE SYSTEMS  

E-Print Network [OSTI]

1 IMPROVEMENTS IN MODELLING DISSOLVED OXYGEN IN ACTIVATED SLUDGE SYSTEMS Jacek Makinia*, Scott A in a full-scale activated sludge reactor. The Activated Sludge Model No. 1 was used to describe for dissolved oxygen. KEYWORDS Activated sludge; dispersion; dissolved oxygen dynamics; mass transfer

Wells, Scott A.

176

Applications of High-Resolution Electrospray Ionization Mass Spectrometry to Measurements of Average Oxygen to Carbon Ratios in Secondary Organic Aerosols  

SciTech Connect (OSTI)

The applicability of high resolution electrospray ionization mass spectrometry (HR ESI-MS) to measurements of the average oxygen to carbon ratio (O/C) in organic aerosols was investigated. Solutions with known average O/C containing up to 10 standard compounds representative of secondary organic aerosol (SOA) were analyzed and corresponding electrospray ionization efficiencies were quantified. The assumption of equal ionization efficiency commonly used in estimating O/C ratios of organic aerosols was found to be reasonably accurate. We found that the accuracy of the measured O/C ratios increases by averaging the values obtained from both (+) and (-) modes. A correlation was found between the ratio of the ionization efficiencies in the positive and negative ESI modes with the octanol-water partition constant, and more importantly, with the compound's O/C. To demonstrate the utility of this correlation for estimating average O/C values of unknown mixtures, we analyzed the ESI (+) and ESI (-) data for SOA produced by oxidation of limonene and isoprene and compared to online O/C measurements using an aerosol mass spectrometer (AMS). This work demonstrates that the accuracy of the HR ESI-MS methods is comparable to that of the AMS, with the added benefit of molecular identification of the aerosol constituents.

Bateman, Adam P.; Laskin, Julia; Laskin, Alexander; Nizkorodov, Sergey

2012-07-02T23:59:59.000Z

177

Heterotrophic Soil Respiration in Warming Experiments: Using Microbial Indicators to Partition Contributions from Labile and Recalcitrant Soil Organic Carbon. Final Report  

SciTech Connect (OSTI)

The central objective of the proposed work was to develop a genomic approach (nucleic acid-based) that elucidates the mechanistic basis for the observed impacts of experimental soil warming on forest soil respiration. The need to understand the mechanistic basis arises from the importance of such information for developing effective adaptation strategies for dealing with projected climate change. Specifically, robust predictions of future climate will permit the tailoring of the most effective adaptation efforts. And one of the greatest uncertainties in current global climate models is whether there will be a net loss of carbon from soils to the atmosphere as climate warms. Given that soils contain approximately 2.5 times as much carbon as the atmosphere, a net loss could lead to runaway climate warming. Indeed, most ecosystem models predict that climate warming will stimulate microbial decomposition of soil carbon, producing such a positive feedback to rising global temperatures. Yet the IPCC highlights the uncertainty regarding this projected feedback. The uncertainty arises because although warming-experiments document an initial increase in the loss of carbon from soils, the increase in respiration is short-lived, declining to control levels in a few years. This attenuation could result from changes in microbial physiology with temperature. We explored possible microbial responses to warming using experiments and modeling. Our work advances our understanding of how soil microbial communities and their activities are structured, generating insight into how soil carbon might respond to warming. We show the importance of resource partitioning in structuring microbial communities. Specifically, we quantified the relative abundance of fungal taxa that proliferated following the addition of organic substrates to soil. We added glycine, sucrose, cellulose, lignin, or tannin-protein to soils in conjunction with 3-bromo-deoxyuridine (BrdU), a nucleotide analog. Active microbes absorb BrdU from the soil solution; if they multiply in response to substrate additions, they incorporate the BrdU into their DNA. After allowing soils to incubate, we extracted BrdU-labeled DNA and sequenced the ITS regions of fungal rDNA. Fungal taxa that proliferated following substrate addition were likely using the substrate as a resource for growth. We found that the structure of active fungal communities varied significantly among substrates. The active fungal community under glycine was significantly different from those under other conditions, while the active communities under sucrose and cellulose were marginally different from each other and the control. These results indicate that the overall community structure of active fungi was altered by the addition of glycine, sucrose, and cellulose and implies that some fungal taxa respond to changes in resource availability. The community composition of active fungi is also altered by experimental warming. We found that glycine-users tended to increase under warming, while lignin-, tannin/protein-, and sucrose-users declined. The latter group of substrates requires extracellular enzymes for use, but glycine does not. It is possible that warming selects for fungal species that target, in particular, labile substrates. Linking these changes in microbial communities and resource partitioning to soil carbon dynamics, we find that substrate mineralization rates are, in general, significantly lower in soils exposed to long-term warming. This suggests that microbial use of organic substrates is impaired by warming. Yet effects are dependent on substrate identity. There are fundamental differences in the metabolic capabilities of the communities in the control and warmed soils. These differences might relate to the changes in microbial community composition, which appeared to be associated with groups specialized on different resources. We also find that functional responses indicate temperature acclimation of the microbial community. There are distinct seasonal patterns and to long-term soil warming, with

Bradford, M A; Melillo, J M; Reynolds, J F; Treseder, K K; Wallenstein, M D

2010-06-10T23:59:59.000Z

178

Refined conceptual model for the Volatile Organic Compounds-Arid Integrated Demonstration and 200 West Area Carbon Tetrachloride Expedited Response Action  

SciTech Connect (OSTI)

This report presents a refined geohydrologic and geochemical conceptual model of the host site (Hanford Reservation) for the Volatile Organic Compounds -- Arid Integrated Demonstration (VOC-Arid ID) and 200 West Area Carbon Tetrachloride (CCl{sub 4}) Expedited Response Action (ERA), based on the results from fiscal year 1992 site characterization activities. The ERA was initiated in December 1990 to minimize or stabilize CCl{sub 4} migration within the unsaturated (vadose) zone in the vicinity of three CCl{sub 4} disposal sites in the 200 West Area (216-Z-1A tile field, 216-Z-9 trench, and 216-Z-18 crib). Implementation of this ERA was based on concerns that CCl{sub 4} residing in the soils was continuing to spread to the groundwater and, if left unchecked, would significantly increase the area of groundwater contamination. A soil-vapor-extraction system began operating at the site in February 1992.

Last, G.V. [Pacific Northwest Lab., Richland, WA (United States); Rohay, V.J. [Westinghouse Hanford Co., Richland, WA (United States)

1993-03-01T23:59:59.000Z

179

Carbon Mineralizability Determines Interactive Effects onMineralizatio...  

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

Determines Interactive Effects onMineralization of Pyrogenic Organic Matter and Soil Organic Carbon. Carbon Mineralizability Determines Interactive Effects onMineralization...

180

The marine geochemistry of dissolved gallium: A comparison with dissolved aluminum  

SciTech Connect (OSTI)

Dissolved Ga concentrations in the pacific Ocean range from 2 to 30 picomolar: they are low in surface waters (2-12 pM), with a subsurface maximum at 150-300 m (6-17 pM), a mid-depth minimum from 500 to 1,000 m (4-10 pM) and increasing values with depth to a maximum in the bottom waters (12-30 pM). The highest concentrations are in the central gyre, with lower values toward the north and east where productivity and particle scavenging increase. Dissolved Ga concentrations in the surface waters of the northwest Atlantic are nearly an order of magnitude higher than in the central North pacific, with higher values in the Gulf Stream than in the continental slope boundary region. The vertical distributions and horizontal transects indicate three sources of dissolved Ga to the oceans. The surface distribution reflects an eolian source with no net fluvial input to the open ocean; the subsurface maximum (a feature not seen for North Pacific dissolved Al) is attributed to vertical exchange processes; the source for the deep waters of the North Pacific is from a sediment surface remineralization process or a pore water flux. Scavenging removal throughout the water column is evident in the vertical profiles for both dissolved Ga and Al, with intensified removal in the boundary regions where productivity and particle scavenging are at a maximum. Residence times of dissolved Ga in surface waters are nearly an order of magnitude longer than the corresponding values for Al.

Orians, K.J.; Bruland, K.W. (Univ. of California, Santa Cruz (USA))

1988-12-01T23:59:59.000Z

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


181

The Arctic Ocean carbon sink G.A. MacGilchrist a,n  

E-Print Network [OSTI]

Carbon sequestration Biological pump a b s t r a c t We present observation based estimatesThe Arctic Ocean carbon sink G.A. MacGilchrist a,n , A.C. Naveira Garabato a , T. Tsubouchi b , S January 2014 Keywords: Arctic Ocean Dissolved inorganic carbon Carbon budget Air­sea carbon dioxide flux

Naveira Garabato, Alberto

182

Carbon Cycle Discussion After the warm-up quiz, discuss the carbon cycle.  

E-Print Network [OSTI]

Carbon Cycle Discussion After the warm-up quiz, discuss the carbon cycle. Carbon is one is without carbon. Where else is carbon on our Earth? In rocks, living organisms, the atmosphere, oceans Does carbon stay in one place? What processes include moving carbon? Introduce residence time: How long does

Carrington, Emily

183

Speciation and structural characterization of plutonium and actinide-organic complexes in surface and groundwaters. 1998 annual progress report  

SciTech Connect (OSTI)

'The authors proposed research is designed to study the association of actinides with dissolved organic complexes in subsurface waters. This study expands considerably on prior work due to the combination of Pu oxidation studies (for Pu speciation/chemical reactivity information), Pu isotope ratio work (for Pu source function information), and the detailed characterization of organic matter in size-fractionated groundwater samples. They have postulated that actinide associations with organic matter may be enhanced due to colloidal biopolymers. This report summarizes work completed after less than 2 years of a 3-year project. Activities thus far have included: (1) the development of sampling techniques to minimize contamination and artifact formation, (2) the separation of Pu isotopes by oxidation state in groundwater, (3) the development of techniques for the separation and identification of organic constituents from natural waters, (4) a study of background Pu and organic carbon concentrations at the proposed study sites, and (5) field work at the Savannah River site (SRS).'

Buesseler, K.O.; Repeta, D.J. [Woods Hole Oceanographic Inst., MA (US); Kelley, J.M. [Pacific Northwest National Lab., Richland, WA (US)

1998-06-01T23:59:59.000Z

184

Use of carbonates for biological and chemical synthesis  

DOE Patents [OSTI]

A system of using carbonates, especially water-insoluble or sparing soluble mineral carbonates, for maintaining or increasing dissolved inorganic carbon concentrations in aqueous media. In particular, the system generates concentrated dissolve inorganic carbon substrates for photosynthetic, chemosynthetic, or abiotic chemical production of carbonaceous or other compounds in solution. In some embodiments, the invention can also enhance the dissolution and retention of carbon dioxide in aqueous media, and can produce pH buffering capacity, metal ions, and heat, which can be beneficial to the preceding syntheses.

Rau, Gregory Hudson

2014-09-09T23:59:59.000Z

185

Changes in soil organic carbon under biofuel crops K R I S T I N A J . A N D E R S O N -T E I X E I R A *, S A R A H C . D AV I S w , M I C H A E L D . M A S T E R S * and  

E-Print Network [OSTI]

Changes in soil organic carbon under biofuel crops K R I S T I N A J . A N D E R S O N - T E I X E of growing biofuel crops will be the sequestration or release of carbon (C) in soil. Soil organic carbon (SOC) represents an important C sink in the lifecycle C balances of biofuels and strongly influences soil quality

DeLucia, Evan H.

186

Effect of Organic Capping Layers over Monodisperse Platinum Nanoparticles upon Activity for Ethylene Hydrogenation and Carbon Monoxide Oxidation  

SciTech Connect (OSTI)

The influence of oleylamine (OA), trimethyl tetradecyl ammonium bromide (TTAB), and polyvinlypyrrolidone (PVP) capping agents upon the catalytic properties of Pt/silica catalysts was evaluated. Pt nanoparticles that were 1.5 nm in size were synthesized by the same procedure (ethylene glycol reduction under basic conditions) with the various capping agents added afterward for stabilization. Before examining catalytic properties for ethylene hydrogenation and CO oxidation, the Pt NPs were deposited onto mesoporous silica (SBA-15) supports and characterized by transmission electron microscopy (TEM), H{sub 2} chemisorption, and elemental analysis (ICP-MS). PVP- and TTAB-capped Pt yielded mass-normalized reaction rates that decreased with increasing pretreatment temperature, and this trend was attributed to the partial coverage of the Pt surface with decomposition products from the organic capping agent. Once normalized to the Pt surface area, similar intrinsic activities were obtained regardless of the pretreatment temperature, which indicated no influence on the nature of the active sites. Consequently, a chemical probe technique using intrinsic activity for ethylene hydrogenation was demonstrated as an acceptable method for estimating the metallic surface areas of Pt. Amine (OA) capping exhibited a detrimental influence on the catalytic properties as severe deactivation and low activity were observed for ethylene hydrogenation and CO oxidation, respectively. These results were consistent with amine groups being strong poisons for Pt surfaces, and revealed the need to consider the effects of capping agents on the catalytic properties.

Kuhn, John N.; Tsung, Chia-Kuang; Huang, Wenyu; Somorjai, Gabor A.

2009-03-24T23:59:59.000Z

187

Determination of Total Solids in Biomass and Total Dissolved...  

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

Total Solids in Biomass and Total Dissolved Solids in Liquid Process Samples Laboratory Analytical Procedure (LAP) Issue Date: 3312008 A. Sluiter, B. Hames, D. Hyman, C. Payne,...

188

On dissolved phosphorus in the Gulf of Mexico  

E-Print Network [OSTI]

: Oceanography ON DISSOLVED PHOSPHOHUS IN THE GULF OF I~1~XICO A Tbesls by DAVID JOHN liRIGHT Approved as to style and content by: l && ~ ~Ohs ' ~f'". . r ead of epact tmen rN 1 tv&ay 1970 ABSTRACT On Dissolved Phosphorus 1n the Gulf of Nexico. (Nay... 1970) David J. Wright, B. S. , Oregon State University; D1rected by: Dr. Lela N. Jeffrey Dissolved phosphorus (P) in the mid-Gulf of Nexico water column during November ranged from 6. l to 79 micro- grams Pjl. In mid-Gulf dissolved inorganic...

Wright, David John

1970-01-01T23:59:59.000Z

189

Variations in dissolved gas compositions of reservoir fluids...  

Open Energy Info (EERE)

A. E.; Copp, J. F. . 111991. Variations in dissolved gas compositions of reservoir fluids from the Coso geothermal field. Proceedings of () ; () : Sixteenth workshop on...

190

,"New York Associated-Dissolved Natural Gas Proved Reserves,...  

U.S. Energy Information Administration (EIA) Indexed Site

Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","New York Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease Separation",10,"Annua...

191

4, 1367, 2007 Modelling carbon  

E-Print Network [OSTI]

BGD 4, 13­67, 2007 Modelling carbon overconsumption and extracellular POC formation M. Schartau et carbon overconsumption and the formation of extracellular particulate organic carbon M. Schartau1 , A Correspondence to: M. Schartau (markus.schartau@gkss.de) 13 #12;BGD 4, 13­67, 2007 Modelling carbon

Paris-Sud XI, Université de

192

Method of making carbon nanotube composite materials  

DOE Patents [OSTI]

The present invention is a method of making a composite polymeric material by dissolving a vinyl thermoplastic polymer, un-functionalized carbon nanotubes and hydroxylated carbon nanotubes and optionally additives in a solvent to make a solution and removing at least a portion of the solvent after casting onto a substrate to make thin films. The material has enhanced conductivity properties due to the blending of the un-functionalized and hydroxylated carbon nanotubes.

O'Bryan, Gregory; Skinner, Jack L; Vance, Andrew; Yang, Elaine Lai; Zifer, Thomas

2014-05-20T23:59:59.000Z

193

Constraining oceanic dust deposition using surface ocean dissolved Al  

E-Print Network [OSTI]

Constraining oceanic dust deposition using surface ocean dissolved Al Qin Han,1 J. Keith Moore,1; accepted 7 December 2007; published 12 April 2008. [1] We use measurements of ocean surface dissolved Al (DEAD) model to constrain dust deposition to the oceans. Our Al database contains all available

Zender, Charles

194

Adaptive Management Team Total Dissolved Gas in the  

E-Print Network [OSTI]

Adaptive Management Team Total Dissolved Gas in the Columbia and Snake Rivers Evaluation of the 115 Percent Total Dissolved Gas Forebay Requirement Washington State Department of Ecology and State of Oregon Department of Environmental Quality Final January 2009 Publication no. 09-10-002 #12;Publication and Contact

195

Bromine and iodine chemistry in a global chemistry-climate model: description and evaluation of very short-lived oceanic sources  

E-Print Network [OSTI]

radiation flux at the surface and the dissolved organic carbon (DOC) con- centration over the ocean.

2012-01-01T23:59:59.000Z

196

The significance of organic carbon and sediment surface area to the benthic biogeochemistry of the slope and deep water environments of the northern Gulf of Mexico  

E-Print Network [OSTI]

at the Geochemical & Environmental Research Group for map construction. I thank Dr. Andreas Luttge and Dr. Rolf Arvidson at Rice University for use of the surface area analyzer. Dr. Luis Cifuentes and Brian Jones at Texas A&M University provided equipment.... ______________ This thesis follows the style and format of Geochimica et Cosmochimica Acta. 2 As the detritus sinks through the water it is subject to break down, or remineralization, by bacterial activity releasing dissolved nutrients to the water...

Beazley, Melanie J.

2004-09-30T23:59:59.000Z

197

E-Print Network 3.0 - alkali metal carbonates Sample Search Results  

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

, sodium carbide, turpentine, finely divided metals Calcium water, carbon dioxide, carbon tetrachloride... , acids, metal powders, sulfur, finely divided organics or...

198

CARBON-CARBON COMPOSITE ALLCOMP Carbon-Carbon Composite  

E-Print Network [OSTI]

materials. MATERIALS AND DESIRED DATA Carbon-Carbon Composites(T300 & SWB): Crush Resistance, Bend StrengthCARBON-CARBON COMPOSITE ALLCOMP Carbon-Carbon Composite · C-C supplied in two forms · T300: C strength 4340 steel, carbon-carbon composite, and Carbon-Silicon Carbide composite were tested to examine

Rollins, Andrew M.

199

ARM - Measurement - Organic Carbon Concentration  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May JunDatastreamsmmcrcalgovInstrumentsruc Documentation RUC : XDCResearch Relatedcontent ARM DatagovMeasurementsNitrogen ARM

200

Organic geochemistry and organic petrography  

SciTech Connect (OSTI)

The Vermillion Creek coals and shales contain dominantly humic organic matter originating from woody plant tissues except for one shale unit above the coals, which contains hydrogen-rich kerogen that is mostly remains of filamentous algae, of likely lacustrine origin. The coals have two unusual features - very low inertinite content and high sulfur content compared to mined western coals. However, neither of these features points to the limnic setting reported for the Vermillion Creek sequence. The vitrinite reflectance of Vermillion Creek shales is markedly lower than that of the coals and is inversely proportional to the H/C ratio of the shales. Rock-Eval pyrolysis results, analyses of H, C, and N, petrographic observations, isotope composition of organic carbon, and amounts and compositions of the CHCl/sub 3/-extractable organic matter all suggest mixtures of two types of organic matter in the Vermillion Creek coals and clay shales: (1) isotopically heavy, hydrogen-deficient, terrestrial organic matter, as was found in the coals, and (2) isotopically light, hydrogen-rich organic matter similar to that found in one of the clay-shale samples. The different compositions of the Vermillion Creek coal, the unnamed Williams Fork Formation coals, and coals from the Middle Pennsylvanian Marmaton and Cherokee Groups are apparently caused by differences in original plant composition, alteration of organic matter related to different pH conditions of the peat swamps, and slightly different organic maturation levels.

Bostick, N.H.; Hatch, J.R.; Daws, T.A.; Love, A.H.; Lubeck, S.C.M.; Threlkeld, C.N.

1987-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


201

Constraining oceanic dust deposition using surface ocean dissolved Al  

E-Print Network [OSTI]

Lett. , 114, 101 – 111. Bruland, K. W. , and M. C. Lohan (K. J. , and K. W. Bruland (1985), Dissolved aluminium in theK. J. , and K. W. Bruland (1986), The biogeochemistry of

Han, Qin; Moore, J. Keith; Zender, Charles; Measures, Chris; Hydes, David

2008-01-01T23:59:59.000Z

202

The marine biogeochemistry of dissolved and colloidal iron  

E-Print Network [OSTI]

Iron is a redox active trace metal micronutrient essential for primary production and nitrogen acquisition in the open ocean. Dissolved iron (dFe) has extremely low concentrations in marine waters that can drive phytoplankton ...

Fitzsimmons, Jessica Nicole

2013-01-01T23:59:59.000Z

203

Diffusional motion of redox centers in carbonate electrolytes  

SciTech Connect (OSTI)

Ferrocene (Fc) and N-(ferrocenylmethyl)-N,N-dimethyl-N-ethylammonium bistrifluoromethyl-sulfonimide (Fc1N112-TFSI) were dissolved in carbonate solvents and self-diffusion coefficients (D) of solutes and solvents were measured by {sup 1}H and {sup 19}F pulsed field gradient nuclear magnetic resonance (NMR) spectroscopy. The organic solvents were propylene carbonate (PC), ethyl methyl carbonate (EMC), and a ternary mixture that also includes ethylene carbonate (EC). Results from NMR studies over the temperature range of 0–50 °C and for various concentrations (0.25–1.7 M) of Fc1N112-TFSI are compared to values of D simulated with classical molecular dynamics (MD). The measured self-diffusion coefficients gradually decreased as the Fc1N112-TFSI concentration increased in all solvents. Since TFSI{sup ?} has fluoromethyl groups (CF{sub 3}), D{sub TFSI} could be measured separately and the values found are larger than those for D{sub Fc1N112} in all samples measured. The EC, PC, and EMC have the same D in the neat solvent mixture and when Fc is dissolved in EC/PC/EMC at a concentration of 0.2 M, probably due to the interactions between common carbonyl structures within EC, PC, and EMC. A difference in D (D{sub PC} < D{sub EC} < D{sub EMC}), and both a higher E{sub a} for translational motion and higher effective viscosity for PC in the mixture containing Fc1N112-TFSI reflect the interaction between PC and Fc1N112{sup +}, which is a relatively stronger interaction than that between Fc1N112{sup +} and other solvent species. In the EC/PC/EMC solution that is saturated with Fc1N112-TFSI, we find that D{sub PC} = D{sub EC} = D{sub EMC} and Fc1N112{sup +} and all components of the EC/PC/EMC solution have the same E{sub a} for translational motion, while the ratio D{sub EC/PC/EMC}/D{sub Fc1N112} is approximately 3. These results reflect the lack of available free volume for independent diffusion in the saturated solution. The Fc1N112{sup +} transference numbers lie around 0.4 and increase slightly as the temperature is increased in the PC and EMC solvents. The trends observed for D from simulations are in good agreement with experimental results and provide molecular level understanding of the solvation structure of Fc1N112-TFSI dissolved in EC/PC/EMC.

Han, Kee Sung [Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington 99352 (United States); Rajput, Nav Nidhi; Persson, Kristin A. [Environmental Energy Technologies Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720 (United States); Wei, Xiaoliang; Wang, Wei [Energy and Environmental Directorate, Pacific Northwest National Laboratory, Richland, Washington 99352 (United States); Hu, Jian Zhi [Fundamental and Computational Sciences Directorate, Pacific Northwest National Laboratory, Richland, Washington 99352 (United States); Mueller, Karl T., E-mail: karl.mueller@pnnl.gov [Environmental Molecular Sciences Laboratory, Pacific Northwest National Laboratory, Richland, Washington 99352 (United States); Department of Chemistry, Pennsylvania State University, University Park, Pennsylvania 16802 (United States)

2014-09-14T23:59:59.000Z

204

Diffusional Motion of Redox Centers in Carbonate Electrolytes  

SciTech Connect (OSTI)

Ferrocene (Fc) and N-(ferrocenylmethyl)-N,N-dimethyl-N-ethylammonium bistrifluoromethyl-sulfonimide (Fc1N112-TFSI) were dissolved in carbonate solvents and self diffusion coefficents (D) of solutes and solvents were measured by 1H and 19F pulsed field gradient (PFG) nuclear magnetic resonance (NMR) spectroscopy. The organic solvents were propylene carbonate (PC), ethyl methyl carbonate (EMC) and a ternary mixture that also includes ethylene carbonate (EC). Results from NMR studies over the temperature range of 0-50 °C and for various concentrations (0.25 - 1.7 M) of Fc1N112-TFSI are compared to values of D simulated with classical molecular dynamics (MD). The measured self-diffusion coefficients gradually decreased as the Fc1N112-TFSI concentration increased in all solvents. Since the peaks for the two ions (Fc1N212 and TFSI) are separated in one-dimensional NMR spectra, separate diffusion coefficients could be measured and DTFSI is larger than DFc1N112 in all samples measured. The EC, PC and EMC have the same D in the neat solvent mixture and when Fc is dissolved in EC/PC/EMC at a concentration of 0.2 M, probably due to the interactions between common carbonyl structures within EC, PC and EMC. A difference in D (DPC < DEC < DEMC), and both a higher Ea for translational motion and higher effective viscosity for PC in the mixture containing Fc1N112-TFSI reflect the interaction between PC and Fc1N112+, which is a relatively stronger interaction than that between Fc1N112+ and other solvent species. In the EC/PC/EMC solution that is saturated with Fc1N112-TFSI, we find that DPC = DEC = DEMC and Fc1N112+ and all components of the EC/PC/EMC solution have the same Ea for translational motion, while the ratio DEC/PC/EMC/DFc1N112+ is approximately 3. These results reflect the lack of available free volume for independent diffusion in the saturated solution. The Fc1N112+ transference numbers lie around 0.4 and increases slightly as the temperature is increased in the PC and EMC solvents. The trends observed for D from simulations are in good agreement with experimental results and provide molecular level understanding of the solvation structure of Fc1N112-TFSI dissolved in EC/PC/EMC.

Han, Kee Sung; Rajput, Nav Nidhi; Wei, Xiaoliang; Wang, Wei; Hu, Jian Z.; Persson, Kristin A.; Mueller, Karl T.

2014-09-14T23:59:59.000Z

205

Carbon ion pump for removal of carbon dioxide from combustion gas and other gas mixtures  

DOE Patents [OSTI]

A novel method and system of separating carbon dioxide from flue gas is introduced. Instead of relying on large temperature or pressure changes to remove carbon dioxide from a solvent used to absorb it from flue gas, the ion pump method, as disclosed herein, dramatically increases the concentration of dissolved carbonate ion in solution. This increases the overlying vapor pressure of carbon dioxide gas, permitting carbon dioxide to be removed from the downstream side of the ion pump as a pure gas. The ion pumping may be obtained from reverse osmosis, electrodialysis, thermal desalination methods, or an ion pump system having an oscillating flow in synchronization with an induced electric field.

Aines, Roger D. (Livermore, CA); Bourcier, William L. (Livermore, CA)

2010-11-09T23:59:59.000Z

206

Carbon ion pump for removal of carbon dioxide from combustion gas and other gas mixtures  

DOE Patents [OSTI]

A novel method and system of separating carbon dioxide from flue gas is introduced. Instead of relying on large temperature or pressure changes to remove carbon dioxide from a solvent used to absorb it from flue gas, the ion pump method, as disclosed herein, dramatically increases the concentration of dissolved carbonate ion in solution. This increases the overlying vapor pressure of carbon dioxide gas, permitting carbon dioxide to be removed from the downstream side of the ion pump as a pure gas. The ion pumping may be obtained from reverse osmosis, electrodialysis, thermal desalination methods, or an ion pump system having an oscillating flow in synchronization with an induced electric field.

Aines, Roger D.; Bourcier, William L.

2014-08-19T23:59:59.000Z

207

Utilization of DNA as a Sole Source of Phosphorus, Carbon, and Energy by Shewanella spp.: Ecological and Physiological Implications for Dissimilatory Metal Reduction  

SciTech Connect (OSTI)

As a constituent of dissolved organic matter, DNA may be consumed by microorganisms inhabiting various freshwater and marine environments. In this study, we demonstrate that dissolved extracellular DNA can serve as a sole source of carbon, energy, nitrogen, and phosphorus for microorganisms residing in the upper layer of Columbia River (WA, USA) water column as well as a sole source of phosphorus for the dissimilatory metal-reducing bacteria Shewanella oneidensis MR-1 and Geobacter sulfurreducens and for Bacillus subtilis ATCC 49760. Our results suggest that DNA assimilation by S. oneidensis is linked to the activity of Ca2+-dependent nuclease(s) and extracellular phosphatase(s). The ability to use DNA as the sole source of phosphorus may be of particular ecological advantage for microorganisms living under Fe(III)-reducing conditions where bioavailability of inorganic phosphate may be limited by the formation of vivianite [Fe3(PO4)2•8H20].

Pinchuk, Grigoriy E.; Ammons, Christine G.; Culley, David E.; Li, Shu-Mei; McLean, Jeffrey S.; Romine, Margaret F.; Nealson, Kenneth H.; Fredrickson, Jim K.; Beliaev, Alex S.

2008-02-15T23:59:59.000Z

208

Correlation of Soil and Sediment Organic Matter Polarity to Aqueous  

E-Print Network [OSTI]

and compared with published partition coefficients (Koc) of carbon tetrachloride (CT) from aqueous solution of the measured partition coefficients (Koc) of carbon tetrachloride (CT) vs. percent polar organic carbon (POC to their organic carbon-normalized sorption coefficients (Koc) for carbon tetrachloride (CT) and 1

209

Continuous surface ocean measurements of dissolved oxygen isotopes  

E-Print Network [OSTI]

Figure 6.2: Fossil fuel emissions perof Carbon Dioxide from Fossil Fuels, editors W. P. Elliott,Carbon dioxide emissions from fossil fuels: A procedure for

Rafelski, Lauren Elmegreen

2012-01-01T23:59:59.000Z

210

alkyl carbonate solution: Topics by E-print Network  

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

R. 13 Solution-processed single walled carbon nanotube electrodes for organic thin-film transistors Physics Websites Summary: t Airbrushed single walled carbon nanotube...

211

Sorted Single-Walled Carbon Nanotube Films for Transparent Electrodes...  

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

Sorted Single-Walled Carbon Nanotube Films for Transparent Electrodes in Organic Solar Cells Home > Research > ANSER Research Highlights > Sorted Single-Walled Carbon Nanotube...

212

Global Proteomics Reveal An Atypical Strategy for Carbon/Nitrogen...  

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

crucial to global oxygen production and worldwide carbon and nitrogen cycles. These microalgae are robust organisms capable carbon neutral biofuel production. Synechocystis sp....

213

PACIFICA (PACIFic ocean Interior CArbon) Database: A Data Synthesis Resource (NDP-92, ORNL/CDIAC-159)  

DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

PACIFICA (PACIFic ocean Interior CArbon) was an international collaborative project for synthesis of data on ocean interior carbon and its related parameters in the Pacific Ocean. The North Pacific Marine Science Organization (PICES), Section on Carbon and Climate (S-CC) supported the project. Hydrographic/hydrochemical datasets have been merged from a total of 272 cruises, including those from cruises conducted between the late 1980s and 2000 but not included in GLODAP, as well as CLIVAR/CO2 Repeat Hydrography datasets from the 2000s. Adjustments were calculated to account for analytical offsets in dissolved inorganic carbon, total alkalinity, salinity, oxygen, and nutrients (nitrate and nitrite, phosphate, and silicic acid) for each cruise as a result of the secondary quality control procedure, based on crossover analysis using data from deep layers (Tanhua et al., 2010). A total of 59 adjusted datasets from Line P off the west coast of Canada were also merged. Finally, the authors have produced the adjusted PACIFICA database that consists of datasets from a total of 306 cruises that also includes 34 datasets from WOCE Hydrographic Program cruises in the Pacific Ocean conducted in the 1990s. The PACIFICA database is available free of charge as a numeric data package (NDP-92) from the Carbon Dioxide Information Analysis Center (CDIAC) and the primary PACIFICA data site at pacifica.pices.jp. The NDP consists of the original cruise data files, adjusted data product, and the documentation.

Suzuki, T.; Ishii, M.; Aoyama, M. R; Christian, J. R.; Enyo, K.; Kawano, T.; Key, R. M.; Kosugi, N.; Kozyr, A.; Miller, L. A.; Murata, A.; Nakano, T.; Ono, T.; Saino, T.; Sasaki, K.; Sasano, D; Takatani, Y.; Wakita, M.; Sabine, C.

214

1994 conceptual model of the carbon tetrachloride contamination in the 200 West Area at the Hanford Site  

SciTech Connect (OSTI)

Between 1955 and 1973, a total of 363,000 to 580,000 L (577,000 to kg) of liquid carbon tetrachloride, in mixtures with other organic and aqueous, actinide-bearing fluids, were discharged to the soil column at three disposal facilities -- the 216-Z-9 Trench, the 216-Z-lA TiTe Field, and the 216-Z-18 Crib -- in the 200 West Area at the Hanford Site. In the mid-1980`s, dissolved carbon tetrachloride was found in the uppermost aquifer beneath the disposal facilities, and in late 1990, the US Environmental Protection Agency and the Washington State Department of Ecology requested that the US Department of Energy proceed with planning and implementation of an expedited response action (ERA) to minimize additional carbon tetrachloride contamination of the groundwater. In February 1992, soil vapor extraction was initiated to remove carbon tetrachloride from the unsaturated zone beneath these disposal facilities. By May 1994, a total of 10,560 L (16,790 kg) of carbon tetrachloride had been removed, amounting to an estimated 2% of the discharged inventory. In the spring of 1991, the Volatile Organic Compounds -- Arid Integrated Demonstration (VOC-Arid ID) program selected the carbon tetrachloride-contaminated site for demonstration and deployment of new technologies for evaluation and cleanup of volatile organic compounds and associated contaminants in soils and groundwater at arid sites. Site investigations conducted in support of both the ERA and the VOC-Arid ID have been integrated because of their shared objective to refine the conceptual model of the site and to promote efficiency. Site characterization data collected in fiscal year 1993 have supported and led to refinement of the conceptual model of the carbon tetrachloride site.

Rohay, V.J.

1994-08-01T23:59:59.000Z

215

PRODUCTION OF CARBON PRODUCTS USING A COAL EXTRACTION PROCESS  

SciTech Connect (OSTI)

This Department of Energy National Energy Technology Laboratory sponsored project developed carbon products, using mildly hydrogenated solvents to extract the organic portion of coal to create synthetic pitches, cokes, carbon foam and carbon fibers. The focus of this effort was on development of lower cost solvents, milder hydrogenation conditions and improved yield in order to enable practical production of these products. This technology is needed because of the long-term decline in production of domestic feedstocks such as petroleum pitch and coal tar pitch. Currently, carbon products represents a market of roughly 5 million tons domestically, and 19 million tons worldwide. Carbon products are mainly derived from feedstocks such as petroleum pitch and coal tar pitch. The domestic supply of petroleum pitch is declining because of the rising price of liquid fuels, which has caused US refineries to maximize liquid fuel production. As a consequence, the long term trend has a decline in production of petroleum pitch over the past 20 years. The production of coal tar pitch, as in the case of petroleum pitch, has likewise declined significantly over the past two decades. Coal tar pitch is a byproduct of metallurgical grade coke (metcoke) production. In this industry, modern metcoke facilities are recycling coal tar as fuel in order to enhance energy efficiency and minimize environmental emissions. Metcoke production itself is dependent upon the production requirements for domestic steel. Hence, several metcoke ovens have been decommissioned over the past two decades and have not been replaced. As a consequence sources of coal tar are being taken off line and are not being replaced. The long-term trend is a reduction in coal tar pitch production. Thus import of feedstocks, mainly from Eastern Europe and China, is on the rise despite the relatively large transportation cost. To reverse this trend, a new process for producing carbon products is needed. The process must be economically competitive with current processes, and yet be environmentally friendly as well. The solvent extraction process developed uses mild hydrogenation of low cost oils to create powerful solvents that can dissolve the organic portion of coal. The insoluble portion, consisting mainly of mineral matter and fixed carbon, is removed via centrifugation or filtration, leaving a liquid solution of coal chemicals and solvent. This solution can be further refined via distillation to meet specifications for products such as synthetic pitches, cokes, carbon foam and fibers. The most economical process recycles 85% of the solvent, which itself is obtained as a low-cost byproduct from industrial processes such as coal tar or petroleum refining. Alternatively, processes have been developed that can recycle 100% of the solvent, avoiding any need for products derived from petroleum or coal tar.

Dady Dadyburjor; Philip R. Biedler; Chong Chen; L. Mitchell Clendenin; Manoj Katakdaunde; Elliot B. Kennel; Nathan D. King; Liviu Magean; Peter G. Stansberry; Alfred H. Stiller; John W. Zondlo

2004-08-31T23:59:59.000Z

216

artery calcium mineral: Topics by E-print Network  

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

between diatom aggregates, minerals, particulate organic carbon, and dissolved organic October 2008. 1 Correlations of particulate organic carbon (POC) and mineral fluxes into...

217

NUMERICALANALYSIS OF FREE SURFACE FLOWS IN FIBER SPINNING OF CARBON NANOTUBES  

E-Print Network [OSTI]

NUMERICALANALYSIS OF FREE SURFACE FLOWS IN FIBER SPINNING OF CARBON NANOTUBES C. Halliburton1 , J Flows in Fiber Spinning of Carbon Nanotubes Charles Halliburton1, J. Alex Lee2, Matteo Pasquali2 1. Nano Acknowledgements ·Fibers can be produced from solutions of carbon nanotubes (CNTs) dissolved in chlorosulphonic

218

The Importance of Carbon Footprint Estimation Boundaries  

E-Print Network [OSTI]

The Importance of Carbon Footprint Estimation Boundaries H . S C O T T M A T T H E W S , C H R I and organizations are pursuing "carbon footprint" projects to estimate their own contributions to global climate change. Protocol definitions from carbon registries help organizations analyze their footprints

Kammen, Daniel M.

219

A Comparative Study of Dolomite Dissolution in Simple Organic Acids and Chelating Agents  

E-Print Network [OSTI]

Acid treatments have predominantly been conducted using HCl for its availability, high rock dissolving power and soluble reaction products. At high temperatures, rapid spending of the acid with carbonates prevents deeper penetration distance...

Adenuga, Olusegun O

2013-05-03T23:59:59.000Z

220

E-Print Network 3.0 - authigenic carbonate formation Sample Search...  

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

in the flux of carbon... to the deep sea. However, the accumulation rate of authigenic uranium depends not only on the organic carbon... into an organic carbon rain rate (export...

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
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221

The solubilities of significant organic compounds in HLW tank supernate solutions -- FY 1995 progress report  

SciTech Connect (OSTI)

At the Hanford Site organic compounds were measured in tank supernate simulant solutions during FY 1995. This solubility information will be used to determine if these organic salts could exist in solid phases (saltcake or sludges) in the waste where they might react violently with the nitrate or nitrite salts present in the tanks. Solubilities of sodium glycolate, succinate, and caproate salts; iron and aluminum and butylphosphate salts; and aluminum oxalate were measured in simulated waste supernate solutions at 25 {degree}C, 30 {degree}C, 40 {degree}C, and 50 {degree}C. The organic compounds were selected because they are expected to exist in relatively high concentrations in the tanks. The solubilities of sodium glycolate, succinate, caproate, and butylphosphate in HLW tank supernate solutions were high over the temperature and sodium hydroxide concentration ranges expected in the tanks. High solubilities will prevent solid sodium salts of these organic acids from precipitating from tank supernate solutions. The total organic carbon concentrations (YOC) of actual tank supernates are generally much lower than the TOC ranges for simulated supernate solutions saturated (at the solubility limit) with the organic salts. This is so even if all the dissolved carbon in a given tank and supernate is due to only one of these eight soluble compounds (an unlikely situation). Metal ion complexes of and butylphosphate and oxalate in supernate solutions were not stable in the presence of the hydroxide concentrations expected in most tanks. Iron and aluminum dibutylphosphate compounds reacted with hydroxide to form soluble sodium dibutylphosphate and precipitated iron and aluminum hydroxides. Aluminum oxalate complexes were also not stable in the basic simulated supernate solutions. Solubilities of all the organic salts decrease with increasing sodium hydroxide concentration because of the common ion effect of Na+. Increasing temperatures raised the solubilities of the organic salts, especially the succinate and caproate salts.

Barney, G.S.

1996-04-26T23:59:59.000Z

222

Interactions of Arsenic and the Dissolved Substances Derived from  

E-Print Network [OSTI]

As trapping and transport within porous soil media and in developing comprehensive plans for managingInteractions of Arsenic and the Dissolved Substances Derived from Turf Soils Z H A N G R O N G C H University, Miami, Florida 33199, Southeast Environmental Research Center, Florida International University

Florida, University of

223

Process for separating dissolved solids from a liquid using an anti-solvent and multiple effect evaporators  

DOE Patents [OSTI]

A process and system are disclosed for treating aluminum salt cake containing water soluble halide salts by contacting the salt cake with water to dissolve water soluble halide salts forming a saturated brine solution. Transporting a portion of about 25% of the saturated brine solution to a reactor and introducing into the saturated brine solution at least an equal volume of a water-miscible low-boiling organic material such as acetone to precipitate a portion of the dissolved halide salts forming a three-phase mixture of an aqueous-organic-salt solution phase and a precipitated salt phase and an organic rich phase. The precipitated salt phase is separated from the other phases and the organic rich phase is recycled to the reactor. The remainder of the saturated brine solution is sent to a multiple effect evaporator having a plurality of stages with the last stage thereof producing low grade steam which is used to boil off the organic portion of the solution which is recycled. 3 figs.

Daniels, E.J.; Jody, B.J.; Bonsignore, P.V.

1994-07-19T23:59:59.000Z

224

JOURNAL OF ENVIRONMENTAL ENGINEERING / SEPTEMBER 2000 / 865 CARBON FIBER ADSORPTION USING QUANTITATIVE  

E-Print Network [OSTI]

JOURNAL OF ENVIRONMENTAL ENGINEERING / SEPTEMBER 2000 / 865 CARBON FIBER ADSORPTION USING carbon fiber (ACF) adsorbents. The DR isotherm parameter, k, depends on the adsorbate as well volatile organic compound adsorbates and activated carbon fiber adsorbents. INTRODUCTION Activated carbon

Cal, Mark P.

225

Investigation on the Charging Process of Li2O2-Based Air Electrodes in Li-O2 Batteries with Organic Carbonate Electrolytes  

SciTech Connect (OSTI)

The charge processes of Li-O2 batteries were investigated by analyzing the gas evolution by in situ gas chromatography-mass spectroscopy (GC/MS) technique. The mixture of Li2O2/Fe3O4/Super P carbon/polyvinylidene fluoride (PVDF) was used as the starting air electrode material and 1M LiTFSI in carbonate-based solvents was used as electrolyte. It was found that Li2O2 is reactive to 1-methyl-2-pyrrolidinone and PVDF binder used in the electrode preparation. During the 1st charge (up to 4.6 V), O2 was the main component in the gases released. The amount of O2 measured by GC/MS was consistent with the amount of Li2O2 decomposed in the electrochemical process as measured by the charge capacity, indicative of the good chargeability of Li2O2. However, after the cell was discharged to 2.0 V in O2 atmosphere and re-charged to ~ 4.6 V in the second cycle, CO2 was dominant in the released gases. Further analysis of the discharged air electrode by X-ray diffraction and Fourier transform infrared spectroscopy indicated that lithium-containing carbonate species (lithium alkyl carbonate and/or Li2CO3) were the main reaction products. Therefore, compatible electrolyte and electrodes as well as the electrode preparation procedures need to be developed for long term operation of rechargeable Li-O2 or Li-air batteries.

Xu, Wu; Viswanathan, Vilayanur V.; Wang, Deyu; Towne, Silas A.; Xiao, Jie; Nie, Zimin; Hu, Dehong; Zhang, Jiguang

2011-04-15T23:59:59.000Z

226

A Physically Based Framework for Modelling the Organic Fractionation of Sea Spray Aerosol from Bubble Film Langmuir Equilibria  

SciTech Connect (OSTI)

The presence of a large fraction of organic matter in primary sea spray aerosol (SSA) can strongly affect its cloud condensation nuclei activity and interactions with marine clouds. Global climate models require new parameterizations of the SSA composition in order to improve the representation of these processes. Existing proposals for such a parameterization use remotely-sensed chlorophyll-a concentrations as a proxy for the biogenic contribution to the aerosol. However, both observations and theoretical considerations suggest that existing relationships with chlorophyll-a, derived from observations at only a few locations, may not be representative for all ocean regions. We introduce a novel framework for parameterizing the fractionation of marine organic matter into SSA based on a competitive Langmuir adsorption equilibrium at bubble surfaces. Marine organic matter is partitioned into classes with differing molecular weights, surface excesses, and Langmuir adsorption parameters. The classes include a lipid-like mixture associated with labile dissolved organic carbon (DOC), a polysaccharide-like mixture associated primarily with semi-labile DOC, a protein-like mixture with concentrations intermediate between lipids and polysaccharides, a processed mixture associated with recalcitrant surface DOC, and a deep abyssal humic-like mixture. Box model calculations have been performed for several cases of organic adsorption to illustrate the underlying concepts. We then apply the framework to output from a global marine biogeochemistry model, by partitioning total dissolved organic carbon into several classes of macromolecule. Each class is represented by model compounds with physical and chemical properties based on existing laboratory data. This allows us to globally map the predicted organic mass fraction of the nascent submicron sea spray aerosol. Predicted relationships between chlorophyll-\\textit{a} and organic fraction are similar to existing empirical parameterizations, but can vary between biologically productive and non-productive regions, and seasonally within a given region. Major uncertainties include the bubble film thickness at bursting and the variability of organic surfactant activity in the ocean, which is poorly constrained. In addition, marine colloids and cooperative adsorption of polysaccharides may make important contributions to the aerosol, but are not included here. This organic fractionation framework is an initial step towards a closer linking of ocean biogeochemistry and aerosol chemical composition in Earth system models. Future work should focus on improving constraints on model parameters through new laboratory experiments or through empirical fitting to observed relationships in the real ocean and atmosphere, as well as on atmospheric implications of the variable composition of organic matter in sea spray.

Burrows, Susannah M.; Ogunro, O.; Frossard, Amanda; Russell, Lynn M.; Rasch, Philip J.; Elliott, S.

2014-12-19T23:59:59.000Z

227

Methods and systems for chemoautotrophic production of organic compounds  

DOE Patents [OSTI]

The present disclosure identifies pathways, mechanisms, systems and methods to confer chemoautotrophic production of carbon-based products of interest, such as sugars, alcohols, chemicals, amino acids, polymers, fatty acids and their derivatives, hydrocarbons, isoprenoids, and intermediates thereof, in organisms such that these organisms efficiently convert inorganic carbon to organic carbon-based products of interest using inorganic energy, such as formate, and in particular the use of organisms for the commercial production of various carbon-based products of interest.

Fischer, Curt R.; Che, Austin J.; Shetty, Reshma P.; Kelly, Jason R.

2013-01-08T23:59:59.000Z

228

Slurried solid media for simultaneous water purification and carbon dioxide removal from gas mixtures  

DOE Patents [OSTI]

A slurried solid media for simultaneous water purification and carbon dioxide removal from gas mixtures includes the steps of dissolving the gas mixture and carbon dioxide in water providing a gas, carbon dioxide, water mixture; adding a porous solid media to the gas, carbon dioxide, water mixture forming a slurry of gas, carbon dioxide, water, and porous solid media; heating the slurry of gas, carbon dioxide, water, and porous solid media producing steam; and cooling the steam to produce purified water and carbon dioxide.

Aines, Roger D.; Bourcier, William L.; Viani, Brian

2013-01-29T23:59:59.000Z

229

Remedial Action Plan and Site Design for Stabilization of the Inactive Uranium Mill Tailings Site, Maybell, Colorado. Appendixes to Attachment 3: Appendix A, Hydrological services calculations: Appendix B, Ground water quality by location, Final report  

SciTech Connect (OSTI)

This report contains chemical analysis data for ground water for the following: elements; cyanides; chlorides; dissolved organic carbon; fluorides; silica; sulfates; sulfides; dissolved solids; nitrates; and nitrites.

Not Available

1994-06-01T23:59:59.000Z

230

Clathrate hydrates in frozen confections : formation by carbon dioxide flash freezing and behavior during distribution and consumption  

E-Print Network [OSTI]

Carbonated frozen foods are not common on the market due to the limited liquid water available to dissolve CO? . CO? clathrate hydrates can change this because CO? is trapped in crystalline water. The CO? flash-freezing ...

Peters, Teresa Baker, 1981-

2009-01-01T23:59:59.000Z

231

Identification of polar, ionic, and highly water soluble organic pollutants in untreated industrial wastewaters  

SciTech Connect (OSTI)

This paper presents a generic protocol for the determination of polar, ionic, and highly water soluble organic pollutants on untreated industrial wastewaters involving the use of two different solid-phase extraction (SPE) methodologies followed by liquid chromatography-mass spectrometry (LC-MS). Untreated industrial wastewaters might contain natural and synthetic dissolved organic compounds with total organic carbon (TOC) values varying between 100 and 3000 mg/L. All polar, ionic and highly water soluble compounds comprising more than 95% of the organic content and with major contribution to the total toxicity of the sample cannot be analyzed by conventional gas chromatography-mass spectrometry (GC-MS), and LC-MS is a good alternative. In this work two extraction procedures were used to obtain fractionated extracts of the nonionic polar compounds: a polymeric Isolute ENV + SPE cartridge for the preconcentration of anionic analytes and a sequential solid-phase extraction (SSPE) method percolating the samples first in octadecylsilica cartridge in series with the polymeric Lichrolut EN cartridge. Average recoveries ranging from 72% to 103% were obtained for a variety of 23 different analytes. Determination of nonionic pollutants was accomplished by reverse-phase liquid chromatography-atmospheric pressure chemical ionization-mass spectrometry (LC-APCI-MS), while anionic compounds were analyzed by ion pair chromatography-electrospray-mass spectrometry (IP-ESI-MS) and LC-ESI-MS. This protocol was applied to a pilot survey of textile and tannery wastewaters leading to the identification and quantification of 33 organic pollutants.

Castillo, M.; Alonso, M.C.; Riu, J.; Barcelo, D. [IIQAB-CSIC, Barcelona (Spain). Dept. of Environmental Chemistry] [IIQAB-CSIC, Barcelona (Spain). Dept. of Environmental Chemistry

1999-04-15T23:59:59.000Z

232

Carbon Capture  

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

Carbon Capture Pre-Combustion Post-Combustion CO2 Compression Systems Analysis Regulatory Drivers Program Plan Capture Handbook Carbon capture involves the separation of CO2 from...

233

Dissolved Oxygen Sensing in a Flow Stream using Molybdenum Chloride Optical Indicators  

E-Print Network [OSTI]

Dissolved Oxygen Sensing in a Flow Stream using Molybdenum Chloride Optical Indicators Reza Loloee1@msu.edu Abstract--Dissolved oxygen concentration is considered the most important water quality variable in fish culture. Reliable and continuous (24/7) oxygen monitoring of dissolved oxygen (DO) in the 1 ­ 11 mg

Ghosh, Ruby N.

234

Carbon dynamics in arctic vegetation   

E-Print Network [OSTI]

Rapid climate change in Arctic regions is of concern due to important feedbacks between the Arctic land surface and the global climate system. A large amount of organic carbon (C) is currently stored in Arctic soils; if ...

Street, Lorna Elizabeth

2011-11-24T23:59:59.000Z

235

Dissolver Off-gas Hot Operations Authorization (AFCI CETE Milestone Report)  

SciTech Connect (OSTI)

The head-end processing of the Coupled-End-to-End (CETE) Demonstration includes fuel receipt, fuel disassembly, exposure of fuel (e.g., by segmenting the fuel pins), voloxidation of the fuel to separate tritium, and fuel dissolution. All of these processing steps with the exception of the dissolution step will be accomplished in the Irradiated Fuels Examination Laboratory (IFEL) (Building 3525). The final headend step will be performed in the Radiochemical Engineering Development Center (Building 7920). The primary purpose of the fuel dissolution step is to prepare the solid fuel for subsequent liquid separations steps. This is accomplished by dissolving the fuel solids using nitric acid. During the dissolution process gases are evolved. Oxides of nitrogen are the primary off-gas components generated by the reactions of nitric acid and the fuel oxides however, during the dissolution and sparging of the resulting solution, iodine, C-14 as carbon dioxide, xenon, and krypton gasses are also released to the off-gas stream. The Dissolver Off-gas treatment rack provides a means of trapping these volatile fission products and other gases via various trapping media. Specifically the rack will recover iodine on a solid sorbent bed, scrub NOx in a water/acid column, scrub CO{sub 2} in a caustic scrubber column, remove moisture with solid sorbent drier beds and recover Xe and Kr using solid absorbent beds. The primary purpose of this experimental rack and the off-gas rack associated with the voloxidation equipment located at IFEL is to close the material balances around the volatile gases and to provide an understanding of the impacts of specific processing conditions on the fractions of the volatile components released from the various head-end processing steps.

Jubin, Robert Thomas [ORNL

2009-06-01T23:59:59.000Z

236

Carbon Smackdown: Carbon Capture  

SciTech Connect (OSTI)

In this July 9, 2010 Berkeley Lab summer lecture, Lab scientists Jeff Long of the Materials Sciences and Nancy Brown of the Environmental Energy Technologies Division discuss their efforts to fight climate change by capturing carbon from the flue gas of power plants, as well as directly from the air

Jeffrey Long

2010-07-12T23:59:59.000Z

237

Carbon Smackdown: Carbon Capture  

ScienceCinema (OSTI)

In this July 9, 2010 Berkeley Lab summer lecture, Lab scientists Jeff Long of the Materials Sciences and Nancy Brown of the Environmental Energy Technologies Division discuss their efforts to fight climate change by capturing carbon from the flue gas of power plants, as well as directly from the air

Jeffrey Long

2010-09-01T23:59:59.000Z

238

Recovery Act: Molecular Simulation of Dissolved Inorganic Carbons for Underground Brine CO2 Sequestration  

SciTech Connect (OSTI)

To further our understanding and develop the method for measuring the DICs under geological sequestration conditions, we studied the infrared spectra of DICs under high pressure and temperature conditions. First principles simulations of DICs in brine conditions were performed using a highly optimized ReaxFF-DIC forcefield. The thermodynamics stability of each species were determined using the 2PT method, and shown to be consistent with the Reax simulations. More importantly, we have presented the IR spectra of DIC in real brine conditions as a function of temperature and pressure. At near earth conditions, we find a breaking of the O-C-O bending modes into asymmetric and symmetric modes, separated by 100cm{sup -1} at 400K and 5 GPa. These results can now be used to calibrate FTIR laser measurements.

Goddard, William

2012-11-30T23:59:59.000Z

239

Dissolved inorganic carbon in soil and shallow groundwater, Konza Prairie LTER Site, NE Kanas, USA  

E-Print Network [OSTI]

cycles of soil air CO2, groundwater DIC, and isotope characteristics showed a strong dependency on weather conditions and soil respiration. Soil air CO2 reached its annual maximum in the middle of the growing season, when moisture was not limiting to soil...

Tsypin, Mikhail

2011-12-31T23:59:59.000Z

240

SciTech Connect: Rapid Field Measurement of Dissolved Inorganic Carbon  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmosphericNuclear Security Administrationcontroller systemsBi (2) Sr (2) Ca (2)Frameworkextended bottom plate.Based on

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


241

Wyoming Associated-Dissolved Natural Gas, Wet After Lease Separation,  

Annual Energy Outlook 2013 [U.S. Energy Information Administration (EIA)]

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary) " ,"ClickPipelinesProved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease

242

Carbon-Based Materials, High-Surface-Area Sorbents, and New Materials...  

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

technologies includes a range of carbon-based materials such as carbon nanotubes, aerogels, nanofibers (including metal-doped hybrids), as well as metal-organic frameworks,...

243

Rapid prototyping of carbon-based chemiresistive gas sensors on paper  

E-Print Network [OSTI]

Chemically functionalized carbon nanotubes (CNTs) are promising materials for sensing of gases and volatile organic compounds. However, the poor solubility of carbon nanotubes hinders their chemical functionalization and ...

Mirica, Katherine

244

Phase partitioning and solubility of iron in natural seawater controlled by dissolved organic matter  

E-Print Network [OSTI]

in the coastal environments [Hutchins and Bruland, 1998; Bruland et al., 2001; Hutchins et al., 2002]. Knowledge

Guo, Laodong

245

Dissolved Organic Matter Cycling on the Louisiana Shelf: Implications for the Formation of Hypoxia  

E-Print Network [OSTI]

................................................................................................... ix LIST OF TABLES .................................................................................................... x CHAPTER I INTRODUCTION ............................................................................... 1 1... .................................. 16 4 DON and Nitrate+Nitrite Pearson Correlation at Stations in August 2010......... 19 5 (A) Pearson product moment correlations (p<0.05) between DFAA and bulk parameters at three stations...

Shen, Li

2012-02-14T23:59:59.000Z

246

A spatial deconvolution of molecular signals in oceanic dissolved organic matter  

E-Print Network [OSTI]

subtropical North Pacific Ocean. Limnol. Oceanogr. 47: 1595-the subtropical North Pacific Ocean. Nature 388: Karl, D. ,subtropical North Pacific Ocean. Nature 388: Kirshenbaum, I;

Meador, Travis Blake

2008-01-01T23:59:59.000Z

247

Oily wastewater treatment: removal of dissolved organic components by forward osmosis.  

E-Print Network [OSTI]

??Produced water is water brought to the surface with crude oil or natural gas; it is the largest waste stream by volume associated with the… (more)

Abousnina, Rajab M

2012-01-01T23:59:59.000Z

248

Absorption and fluorescence of chromophoric dissolved organic matter in the Pearl River Estuary, South China  

E-Print Network [OSTI]

plant decay matter: tryptophan-like fluorophore T had the strongest signal among all fluorophores originates from degradation of plant materials in terrestrial and aquatic ecosystems (Kirk, 1994). It plays in prin- ciple be determined with remote sensing techniques. In offshore waters, CDOM is presumably

249

Dissolved organic matter discharge in the six largest arctic rivers-chemical composition and seasonal variability  

E-Print Network [OSTI]

) -1 , c) Acid to aldehyde ratios for vanillyls and syringyls, d) Syringyls/Vanillyls (S/V) & Cinnamyls/ vanillyls (C/V), e) p-coumaric acid/ferulic acid (CAD/FAD) & p- hydroxybenzaldehyde /total p-hydroxy group (PON/P), f) 3,5...-hydroxy group (PON/P), f) 3,5- dihydroxybenzoic acid/vanillyl (DiBA/V) & total p-hydroxy group/ (vanillyl + syringyl) (P/(V+S))............................................................... 72 27 Kolyma River discharge (m 3 s -1 ), and a...

Rinehart, Amanda J.

2009-05-15T23:59:59.000Z

250

A Spatial Deconvolution of Molecular Signals in Oceanic Dissolved Organic Matter  

E-Print Network [OSTI]

subtropical North Pacific Ocean. Limnol. Oceanogr. 47: 1595-the subtropical North Pacific Ocean. Nature 388: Karl, D. ,central equatorial Pacific Ocean, 1992: Daily and finescale

Meador, Travis B

2008-01-01T23:59:59.000Z

251

The Effects of Ozone Deposition and Dissolved Organic Matter on Manganese Speciation in the Surface Ocean  

E-Print Network [OSTI]

such as humics and is strongly enhanced by the presence of light (Spokes and Liss 1995; Sunda and Huntsman 1994). Spokes and Liss (1995) showed that an increase in the concentration of humic acid in solution leads to an increase in the rate of photoreduction... deposition to seawater (Reckhow et al. 1991). The formation of MnO2 in drinking water has been studied with respect to humic acids and bicarbonate, both of which could be important in seawater. Humics compete with Mn(II) for O3, increasing the amount of O3...

Smyth, Alison Michelle

2014-07-31T23:59:59.000Z

252

Sources and Fate of Chromophoric Dissolved Organic Matter in the Arctic Ocean and Surrounding Watersheds  

E-Print Network [OSTI]

Drift UHW Upper halocline water layer WGC West Greenland Current ix TABLE OF CONTENTS Page ABSTRACT... .................................................................................................. vii TABLE OF CONTENTS .......................................................................................... ix LIST OF FIGURES ................................................................................................... xii LIST...

Walker, Sally Annette

2012-10-19T23:59:59.000Z

253

Author's personal copy Modeling the dynamics and export of dissolved organic matter in the  

E-Print Network [OSTI]

& Mary, Route 1208, Greate Road, Gloucester Point, VA 23062-1346, USA c Rutgers University, 71 Dudley), mesotrophic (Anderson and Williams, 1998; Fasham et al., 1999) and oligotro- phic (Anderson and Pondaven, 2003; Raick et al., 2005) regional systems and the global ocean (Popova and Anderson, 2002). Fasham et al

Fennel, Katja

254

VOLUME 89, NUMBER 1 P H Y S I C A L R E V I E W L E T T E R S 1 JULY 2002 Self-Organization of a Carbide Superlattice during Deposition of Carbon on Mo  

E-Print Network [OSTI]

of carbides in transition metals has long been a subject of interest since the Industrial Revolution. Re- cently, many of the same transition metals have been used as catalysts for the production of single-Organization of a Carbide Superlattice during Deposition of Carbon on Mo F. Tsui* and P. A. Ryan Department of Physics

255

Carbon nanotube coatings as chemical absorbers  

DOE Patents [OSTI]

Airborne or aqueous organic compound collection using carbon nanotubes. Exposure of carbon nanotube-coated disks to controlled atmospheres of chemical warefare (CW)-related compounds provide superior extraction and retention efficiencies compared to commercially available airborne organic compound collectors. For example, the carbon nanotube-coated collectors were four (4) times more efficient toward concentrating dimethylmethyl-phosphonate (DMMP), a CW surrogate, than Carboxen, the optimized carbonized polymer for CW-related vapor collections. In addition to DMMP, the carbon nanotube-coated material possesses high collection efficiencies for the CW-related compounds diisopropylaminoethanol (DIEA), and diisopropylmethylphosphonate (DIMP).

Tillotson, Thomas M.; Andresen, Brian D.; Alcaraz, Armando

2004-06-15T23:59:59.000Z

256

Influence of Carbon Sources and Electron Shuttles on Ferric Iron Reduction by Cellulomonas sp. Strain ES6  

SciTech Connect (OSTI)

Microbially reduced iron minerals can reductively transform a variety of contaminants including heavy metals, radionuclides, chlorinated aliphatics, and nitroaromatics. A number of Cellulomonas spp. strains, including strain ES6, isolated from aquifer samples obtained at the U.S. Department of Energy's Hanford site in Washington, have been shown to be capable of reducing Cr(VI), TNT, natural organic matter, and soluble ferric iron [Fe(III)]. This research investigated the ability of Cellulomonas sp. strain ES6 to reduce solid phase and dissolved Fe(III) utilizing different carbon sources and various electron shuttling compounds. Results suggest that Fe(III) reduction by and growth of strain ES6 was dependent upon the type of electron donor, the form of iron present, and the presence of synthetic or natural organic matter, such as anthraquinone-2,6-disulfonate (AQDS) or humic substances. This research suggests that Cellulomonas sp. strain ES6 could play a significant role in metal reduction in the Hanford subsurface and that the choice of carbon source and organic matter addition can allow for independent control of growth and iron reduction activity.

Dr Robin Gerlach; Erin K. Field; Sridhar Viamajala; Brent M. Peyton; William A. Apel; Al B. Cunningham

2011-09-01T23:59:59.000Z

257

Introduction to carbon physics Carbon is in many ways a unique element. Most importantly, it is crucial for life on earth as  

E-Print Network [OSTI]

out of carbon. Scientifically, the whole huge field of organic chemistry deals entirely with carbon with producing nanotubes with specific properties. A number of reviews and books about carbon nanotubes have been

Johannesson, Henrik

258

Bankruptcy, guns or campaigns : explaining armed organizations' post-war trajectories  

E-Print Network [OSTI]

This project seeks to explain what happens to armed organizations after they sign peace accords. Why do they dissolve, return to war, or form non-violent socio-political entities (political parties or civic associations)? ...

Daly, Sarah Zukerman

2011-01-01T23:59:59.000Z

259

Speciation and structural characterization of plutonium and actinide-organic complexes in surface and groundwaters. 1998 annual progress report  

SciTech Connect (OSTI)

'The authors proposed research is designed to study the association of actinides with dissolved organic complexes in subsurface waters. This study expands considerably on prior work due to the combination of Pu oxidation studies (for Pu speciation/chemical reactivity information), Pu isotope ratio work (for Pu source function information), and the detailed characterization of organic matter in size-fractionated groundwater samples. The authors have postulated that actinide associations with organic matter may be enhanced due to colloidal biopolymers. This report summarizes work completed after less than 2 years of a 3-year project. Activities thus far have included: (1) the development of sampling techniques to minimize contamination and artifact formation, (2) the separation of Pu isotopes by oxidation state in groundwater, (3) the development of techniques for the separation and identification of organic constituents from natural waters, (4) a study of background Pu and organic carbon concentrations at the proposed study sites, and (5) field work at the Savannah River Site (SRS).'

Buesseler, K.O.; Repeta, D.J. [Woods Hole Oceanographic Inst., Woods Hole, MA (US); Kelley, J.M. [Pacific Northwest National Lab., Richland, WA (US)

1998-06-01T23:59:59.000Z

260

Lesson Summary Students will learn about different carbon  

E-Print Network [OSTI]

Lesson Summary Students will learn about different carbon sources and sinks and the release · Knowledge of carbon as the main constituent of living organisms AAAS Science Benchmarks The Physical Setting Materials · 1 copy of The Carbon Cycle (Figure 1) · 1 copy of The Carbon Cycle A4 sheet for each student · 1

Mojzsis, Stephen J.

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


261

Evaluation and validation of criticality codes for fuel dissolver calculations  

SciTech Connect (OSTI)

During the past ten years an OECD/NEA Criticality Working Group has examined the validity of criticality safety computational methods. International calculation tools which were shown to be valid in systems for which experimental data existed were demonstrated to be inadequate when extrapolated to fuel dissolver media. The spread of the results in the international calculation amounted to {plus minus} 12,000 pcm in the realistic fuel dissolver exercise n{degrees} 19 proposed by BNFL, and to {plus minus} 25,000 pcm in the benchmark n{degrees} 20 in which fissile material in solid form is surrounded by fissile material in solution. A theoretical study of the main physical parameters involved in fuel dissolution calculations was performed, i.e. range of moderation, variation of pellet size and the fuel double heterogeneity effect. The APOLLO/P{sub IC} method developed to treat latter effect, permits us to supply the actual reactivity variation with pellet dissolution and to propose international reference values. The disagreement among contributors' calculations was analyzed through a neutron balance breakdown, based on three-group microscopic reaction rates solicited from the participants. The results pointed out that fast and resonance nuclear data in criticality codes are not sufficiently reliable. Moreover the neutron balance analysis emphasized the inadequacy of the standard self-shielding formalism (NITAWL in the international SCALE package) to account for {sup 238}U resonance mutual self-shielding in the pellet-fissile liquor interaction. Improvements in the up-dated 1990 contributions, as do recent complementary reference calculations (MCNP, VIM, ultrafine slowing-down CGM calculation), confirm the need to use rigorous self-shielding methods in criticality design-oriented codes. 6 refs., 11 figs., 3 tabs.

Santamarina, A.; Smith, H.J. (CEA Centre d'Etudes Nucleaires de Cadarache, 13 - Saint-Paul-lez-Durance (France)); Whitesides, G.E. (Oak Ridge National Lab., TN (United States))

1991-01-01T23:59:59.000Z

262

Effect of raw material and Kraft Pulping Conditions on Characteristics of Dissolved Lignin.  

E-Print Network [OSTI]

?? Lignin is one of the main components in wood and during the chemical pulping processes it is degraded and dissolved into the cooking liquor.… (more)

Svärd, Antonia

2014-01-01T23:59:59.000Z

263

Enhanced terrestrial carbon uptake in the Northern High Latitudes in the 21st century from the Coupled Carbon  

E-Print Network [OSTI]

the Coupled Carbon Cycle Climate Model Intercomparison Project model projections H A I F E N G Q I A N *, R E Carbon Cycle Climate Model Intercomparison Project. Our analysis suggests that the NHL will be a carbon the intense warming there enhances SOM decomposition, soil organic carbon (SOC) storage continues to increase

Zeng, Ning

264

The temporal dynamics of terrestrial organic matter transfer to the oceans : initial assessment and application  

E-Print Network [OSTI]

This thesis employs compound-specific stable carbon and radiocarbon isotopic analysis of organic biomarkers to (a) resolve petrogenic from pre-aged vascular plant organic carbon (OC) in continental margin sediments, (b) ...

Drenzek, Nicholas J

2007-01-01T23:59:59.000Z

265

Storage and turnover of organic matter in soil  

E-Print Network [OSTI]

of organic carbon from peat soils. Nature 412 , 785. Fried,Plant Litter. Standard Soil Methods for Long-Term Ecological2007). Role of proteins in soil carbon and nitrogen storage:

Torn, M.S.

2009-01-01T23:59:59.000Z

266

1 In situ Ramanbased measurements of high dissolved methane 2 concentrations in hydraterich ocean sediments  

E-Print Network [OSTI]

sediments 3 Xin Zhang,1,2 Keith C. Hester,1,3 William Ussler,1 Peter M. Walz,1 Edward T. Peltzer,1 4 XX Month 2011. 6 [1] Ocean sediment dissolved CH4 concentrations are of 7 interest for possible dissolved 28 methane concentrations in hydraterich ocean sediments, Geophys. 29 Res. Lett., 38, LXXXXX, doi

Tian, Weidong

267

Effects of applied voltages and dissolved oxygen on sustained power generation by microbial fuel cells  

E-Print Network [OSTI]

Effects of applied voltages and dissolved oxygen on sustained power generation by microbial fuel), Faculty of Advanced Technology, University of Glamorgan, Pontypridd RCT CF37 1DL, UK Oxygen intrusion chamber MFCs at the end of a cycle when the substrate is depleted. A slight increase in dissolved oxygen

268

Constraining Oceanic dust deposition using surface 1 ocean dissolved Al 2  

E-Print Network [OSTI]

Constraining Oceanic dust deposition using surface 1 ocean dissolved Al 2 Qin Han, J. Keith Moore, Charles Zender, Chris Measures, David Hydes 3 Abstract 4 We use measurements of ocean surface dissolved Al and Deposition 6 (DEAD) model, to constrain dust deposition to the oceans. Our Al database contains 7 all

Zender, Charles

269

Dissolved oxygen stratification in two micro-tidal partially-mixed estuaries  

E-Print Network [OSTI]

Dissolved oxygen stratification in two micro-tidal partially-mixed estuaries Jing Lin a,*, Lian Xie online 21 August 2006 Abstract The controlling physical factors for vertical oxygen stratification that vertical stratification of dissolved oxygen (DO) concentration can be explained by the extended Hansen

Mallin, Michael

270

Isolation and Quantification of Dissolved Lignin from Natural Waters Using Solid-Phase Extraction  

E-Print Network [OSTI]

Isolation and Quantification of Dissolved Lignin from Natural Waters Using Solid-Phase Extraction) was tested for the isolation of dissolved lignin from diverse natural waters (fresh, estuarine, and marine and quantification of trace levels of lignin in seawater. The low blanks and quick cleanup of C18 cartridges support

Louchouarn, Patrick

271

Dissolved Gas in the Snake and Columbia Rivers Modeled by CRiSP  

E-Print Network [OSTI]

Dissolved Gas in the Snake and Columbia Rivers 1969-1984 Modeled by CRiSP Pamela Shaw Columbia Basin Research School of Fisheries, UW #12;Introduction These dissolved gas profiles for 1969-1984 were created using CRiSP and historic spill and flow data. In CRiSP the gas going into the tailwater

Washington at Seattle, University of

272

Flowsheet modifications for dissolution of sand, slag, and crucible residues in the F-canyon dissolvers  

SciTech Connect (OSTI)

An initial flowsheet for the dissolution of sand, slag, and crucible (SS{ampersand}C) was developed for the F- Canyon dissolvers as an alternative to dissolution in FB-Line. In that flowsheet, the sand fines were separated from the slag chunks and crucible fragments. Those two SS{ampersand}C streams were packaged separately in mild-steel cans for dissolution in the 6.4D dissolver. Nuclear safety constraints limited the dissolver charge to approximately 350 grams of plutonium in two of the three wells of the dissolver insert and required 0.23M (molar) boron as a soluble neutron poison in the 9.3M nitric acid/0.013M fluoride dissolver solution. During the first dissolution of SS{ampersand}C fines, it became apparent that a significant amount of the plutonium charged to the 6.4D dissolver did not dissolve in the time predicted by previous laboratory experiments. The extended dissolution time was attributed to fluoride complexation by boron. An extensive research and development (R{ampersand}D) program was initiated to investigate the dissolution chemistry and the physical configuration of the dissolver insert to understand what flowsheet modifications were needed to achieve a viable dissolution process.

Rudisill, T.S.; Karraker, D.G.; Graham, F.R.

1997-12-01T23:59:59.000Z

273

Intermediate Temperature Carbon - Carbon Composite Structures. CRADA Final Report  

SciTech Connect (OSTI)

The objective of this Cooperative Research and Development Agreement (CRADA) between UT-Battelle, LLC (the "Contractor") and Synterials, Inc. (the "Participant") was to demonstrate promising processing methods, which can lead to producing Carbon-Carbon Composites (CCC), with tensile and interlaminar properties comparable to those of organic matrix composites and environmental stability at 1200 F for long periods of time. The participant synthesized carbon-carbon composites with two different fiber coatings and three different matrices. Both parties evaluated the tensile and interlaminar properties of these materials and characterized the microstructure of the matrices and interfaces. It was found that fiber coatings of carbon and boron carbide provided the best environmental protection and resulted in composites with high tensile strength.

Lara-Curzio, Edgar [ORNL

2007-06-01T23:59:59.000Z

274

Carbon Nanotubes.  

E-Print Network [OSTI]

?? Carbon nanotubes have extraordinary mechanical, electrical, thermal andoptical properties. They are harder than diamond yet exible, have betterelectrical conductor than copper, but can also… (more)

Fredriksson, Tore

2014-01-01T23:59:59.000Z

275

The Transfer of Dissolved Cs-137 from Soil to Plants  

SciTech Connect (OSTI)

Rapidly maturing plants were grown simultaneously at the same experimental sites under natural conditions at the Chernobyl Exclusion Zone. Roots of the plants were side by side in the soil. During two seasons we selected samples of the plants and of the soils several times every season. Content of Cs-137 in the plant and in the soil solution extracted from the samples of soils was measured. Results of measurements of the samples show that, for the experimental site, Cs-137 content in the plant varies with date of the sample selection. The plant:soil solution Cs-137 concentration ratio depends strongly on the date of selection and also on the type of soil. After analysis of the data we conclude that Cs-137 plant uptake is approximately proportional to the content of dissolved Cs-137 in the soil per unit of volume, and the plant:soil solution Cs-137 concentration ratio for the soil is approximately proportional to the soil moisture. (authors)

Prorok, V.V.; Melnichenko, L.Yu. [Department of Physics, Taras Shevchenko National University of Kyiv, 2, build. 1 Acad. Glushkov prospect, Kyiv-680 MSP (Ukraine); Mason, C.F.V. [Research Applications Corporation, 148 Piedra Loop, Los Alamos, NM 87544 (United States); Ageyev, V.A.; Ostashko, V.V. [Institute for Nuclear Research, 47 Nauky prospect, Kyiv-680 MSP (Ukraine)

2006-07-01T23:59:59.000Z

276

Training Graduate and Undergraduate Students in Simulation and Risk Assessment for Carbon Sequestration  

SciTech Connect (OSTI)

Capturing carbon dioxide (CO2) and injecting it into deep underground formations for storage (carbon capture and underground storage, or CCUS) is one way of reducing anthropogenic CO2 emissions. Gas or aqueous-phase leakage may occur due to transport via faults and fractures, through faulty well bores, or through leaky confining materials. Contaminants of concern include aqueous salts and dissolved solids, gaseous or aqueous-phase organic contaminants, and acidic gas or aqueous-phase fluids that can liberate metals from aquifer minerals. Understanding the mechanisms and parameters that can contribute to leakage of the CO2 and the ultimate impact on shallow water aquifers that overlie injection formations is an important step in evaluating the efficacy and risks associated with long-term CO2 storage. Three students were supported on the grant Training Graduate and Undergraduate Students in Simulation and Risk Assessment for Carbon Sequestration. These three students each examined a different aspect of simulation and risk assessment related to carbon dioxide sequestration and the potential impacts of CO2 leakage. Two performed numerical simulation studies, one to assess leakage rates as a function of fault and deep reservoir parameters and one to develop a method for quantitative risk assessment in the event of a CO2 leak and subsequent changes in groundwater chemistry. A third student performed an experimental evaluation of the potential for metal release from sandstone aquifers under simulated leakage conditions. This study has resulted in two student first-authored published papers {Siirila, 2012 #560}{Kirsch, 2014 #770} and one currently in preparation {Menke, In prep. #809}.

McCray, John

2013-09-30T23:59:59.000Z

277

Sorbents and Carbon-Based Materials for Hydrogen Storage R &...  

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

for storing hydrogen in high-surface-area sorbents such as hybrid carbon nanotubes, aerogels, and nanofibers, as well as metal-organic frameworks and conducting polymers. A...

278

Sorbents and Carbon-Based Materials for Hydrogen Storage Research...  

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

for storing hydrogen in high-surface-area sorbents such as hybrid carbon nanotubes, aerogels, and nanofibers, as well as metal-organic frameworks and conducting polymers. A...

279

Graphene Produces More Efficient Charge Transport Inside an Organic  

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

Graphene Produces More Efficient Charge Transport Inside an Organic Semiconductor Graphene, a two dimensional semi-metal made of sp 2 hybridized carbon, is an outstanding material...

280

Graphene Produces More Efficient Charge Transport Inside an Organic...  

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

Graphene Produces More Efficient Charge Transport Inside an Organic Semiconductor Friday, January 30, 2015 Graphene, a two dimensional semi-metal made of sp2 hybridized carbon, is...

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


281

ccsd00003923, Combination of carbon nanotubes and  

E-Print Network [OSTI]

of composite optical limiters, in which two complementary nonlinear optical materials are mixed togetherccsd­00003923, version 1 ­ 18 Jan 2005 Combination of carbon nanotubes and two-photon absorbers-linear scattering from single-wall carbon nanotubes (SWNT) and multiphoton absorption (MPA) from organic

282

Gas adsorption on metal-organic frameworks  

DOE Patents [OSTI]

The present invention involves the use of certain metal organic frameworks that have been treated with water or another metal titrant in the storage of carbon dioxide. The capacity of these frameworks is significantly increased through this treatment.

Willis, Richard R. (Cary, IL); Low, John J. (Schaumburg, IL), Faheem, Syed A. (Huntley, IL); Benin, Annabelle I. (Oak Forest, IL); Snurr, Randall Q. (Evanston, IL); Yazaydin, Ahmet Ozgur (Evanston, IL)

2012-07-24T23:59:59.000Z

283

Organic aerogel microspheres  

DOE Patents [OSTI]

Organic aerogel microspheres are disclosed which can be used in capacitors, batteries, thermal insulation, adsorption/filtration media, and chromatographic packings, having diameters ranging from about 1 micron to about 3 mm. The microspheres can be pyrolyzed to form carbon aerogel microspheres. This method involves stirring the aqueous organic phase in mineral oil at elevated temperature until the dispersed organic phase polymerizes and forms nonstick gel spheres. The size of the microspheres depends on the collision rate of the liquid droplets and the reaction rate of the monomers from which the aqueous solution is formed. The collision rate is governed by the volume ratio of the aqueous solution to the mineral oil and the shear rate, while the reaction rate is governed by the chemical formulation and the curing temperature.

Mayer, S.T.; Kong, F.M.; Pekala, R.W.; Kaschmitter, J.L.

1999-06-01T23:59:59.000Z

284

Organic aerogel microspheres  

DOE Patents [OSTI]

Organic aerogel microspheres which can be used in capacitors, batteries, thermal insulation, adsorption/filtration media, and chromatographic packings, having diameters ranging from about 1 micron to about 3 mm. The microspheres can be pyrolyzed to form carbon aerogel microspheres. This method involves stirring the aqueous organic phase in mineral oil at elevated temperature until the dispersed organic phase polymerizes and forms nonsticky gel spheres. The size of the microspheres depends on the collision rate of the liquid droplets and the reaction rate of the monomers from which the aqueous solution is formed. The collision rate is governed by the volume ratio of the aqueous solution to the mineral oil and the shear rate, while the reaction rate is governed by the chemical formulation and the curing temperature.

Mayer, Steven T. (San Leandro, CA); Kong, Fung-Ming (Pleasanton, CA); Pekala, Richard W. (Pleasant Hill, CA); Kaschmitter, James L. (Pleasanton, CA)

1999-01-01T23:59:59.000Z

285

Carbon Fiber  

ScienceCinema (OSTI)

Lee McGetrick leads ORNL's effort to produce light, durable carbon fiber at lower cost -- a key to improvements in manufacturing that will produce more fuel-efficient vehicles and other advances.

McGetrick, Lee

2014-07-23T23:59:59.000Z

286

Carbon Fiber  

SciTech Connect (OSTI)

Lee McGetrick leads ORNL's effort to produce light, durable carbon fiber at lower cost -- a key to improvements in manufacturing that will produce more fuel-efficient vehicles and other advances.

McGetrick, Lee

2014-04-17T23:59:59.000Z

287

Carbon Sequestration  

SciTech Connect (OSTI)

Carbon Sequestration- the process of capturing the CO2 released by the burning of fossil fuels and storing it deep withing the Earth, trapped by a non-porous layer of rock.

None

2013-05-06T23:59:59.000Z

288

Source Term Modeling for Evaluating the Potential Impacts to Groundwater of Fluids Escaping from a Depleted Oil Reservoir Used for Carbon Sequestration  

SciTech Connect (OSTI)

In recent years depleted oil reservoirs have received special interest as carbon storage reservoirs because of their potential to offset costs through collaboration with enhanced oil recovery projects. Modeling is currently being conducted to evaluate potential risks to groundwater associated with leakage of fluids from depleted oil reservoirs used for storage of CO2. Modeling results reported here focused on understanding how toxic organic compounds found in oil will distribute between the various phases within a storage reservoir after introduction of CO2, understanding the migration potential of these compounds, and assessing potential groundwater impacts should leakage occur. Two model scenarios were conducted to evaluate how organic components in oil will distribute among the phases of interest (oil, CO2, and brine). The first case consisted of 50 wt.% oil and 50 wt.% water; the second case was 90 wt.% CO2 and 10 wt.% oil. Several key organic compounds were selected for special attention in this study based upon their occurrence in oil at significant concentrations, relative toxicity, or because they can serve as surrogate compounds for other more highly toxic compounds for which required input data are not available. The organic contaminants of interest (COI) selected for this study were benzene, toluene, naphthalene, phenanthrene, and anthracene. Partitioning of organic compounds between crude oil and supercritical CO2 was modeled using the Peng-Robinson equation of state over temperature and pressure conditions that represent the entire subsurface system (from those relevant to deep geologic carbon storage environments to near surface conditions). Results indicate that for a typical set of oil reservoir conditions (75°C, and 21,520 kPa) negligible amounts of the COI dissolve into the aqueous phase. When CO2 is introduced into the reservoir such that the final composition of the reservoir is 90 wt.% CO2 and 10 wt.% oil, a significant fraction of the oil dissolves into the vapor phase. As the vapor phase moves up through the stratigraphic column, pressures and temperatures decrease, resulting in significant condensation of oil components. The heaviest organic components condense early in this process (at higher pressures and temperatures), while the lighter components tend to remain in the vapor phase until much lower pressures and temperatures are reached. Based on the model assumptions, the final concentrations of COI to reach an aquifer at 1,520 kPa and 25°C were quite significant for benzene and toluene, whereas the concentrations of polynuclear aromatic hydrocarbons that reach the aquifer were very small. This work demonstrates a methodology that can provide COI source term concentrations in CO2 leaking from a reservoir and entering an overlying aquifer for use in risk assessments.

Cantrell, Kirk J.; Brown, Christopher F.

2014-06-13T23:59:59.000Z

289

Dissolved strontium in the subterranean estuary Implications for the marine strontium isotope budget  

E-Print Network [OSTI]

Dissolved strontium in the subterranean estuary ­ Implications for the marine strontium isotope concentrations among sites (0.1­24 lM Sr). Strontium isotope exchange was observed in the STE at five

290

E-Print Network 3.0 - actual icpp dissolved Sample Search Results  

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

for: actual icpp dissolved Page: << < 1 2 3 4 5 > >> 1 RAC Report No. 4-CDC-Task Order 1-1999-Final FINAL REPORT Summary: and chromium concentrations in air from suspension...

291

Corrosion mechanisms in aqueous solutions containing dissolved H2S. Part 2: Mode! ofthe cathodic reactions.  

E-Print Network [OSTI]

Corrosion mechanisms in aqueous solutions containing dissolved H2S. Part 2: Mode! ofthe cathodicFP Energies nouvelles, Rond-point de 1'Ă©changeur de Solaize BP3, 69360 Solaize, France. J. Corrosion

Paris-Sud XI, Université de

292

BOOKS & MEDIA UPDATE Carbon Nanotechnology  

E-Print Network [OSTI]

of organic semiconductors are introduced in this book, which also gives a clear impression of the rangeBOOKS & MEDIA UPDATE Carbon Nanotechnology Liming Dai (ed.) Elsevier · 2006 · 750 pp ISBN: 0 are reviewed. Contributions by different authors are grouped into three sections on the synthesis, chemistry

Elliott, James

293

AMAZING CARBON Prof. David Tomnek  

E-Print Network [OSTI]

understood. The complexity and importance of Organic Chemistry reflects the fact that chemically, or gasoline. Without carbon, the key player in molecular biology, our life would be different, or not exist enough to warrant the 1996 Chemistry Nobel prize for Smalley, Kroto and Curl. The amazing world of sub

294

EXPERIMENTAL STUDY TO EVALUATE CORROSION OF THE F-CANYON DISSOLVER DURING THEUNIRRADIATED MARK-42 CAMPAIGN  

SciTech Connect (OSTI)

Unirradiated Mark 42 fuel tubes are to be dissolved in an upcoming campaign in F-canyon. Savannah River Technology Center (SRTC)/Chemical & Hydrogen Technology Section (CHTS) identified a flow sheet for the dissolution of these Mark 42 fuel tubes which required a more aggressive dissolver solution than previously required for irradiated Mark 42 fuel tubes. Subsequently, SRTC/MTS was requested to develop and perform a corrosion testing program to assess the impact of new flow sheets on corrosion of the dissolver wall. The two primary variables evaluated were the fluoride and aluminum concentrations of the dissolver solution. Fluoride was added as Calcium Fluoride (CaF{sub 2}) while the aluminum was added either as metallic aluminum, which was subsequently dissolved, or as the chemical aluminum nitrate (Al(NO{sub 3}){sub 3}). The dissolved aluminum metal was used to simulate the dissolution of the aluminum from the Mark 42 cladding and fuel matrix. Solution composition for the corrosion tests bracketed the flow sheet for the Mark 42. Corrosion rates of AISI Type 304 stainless steel coupons, both welded and non-welded coupons, were calculated from measured weight losses and post-test concentrations of soluble Fe, Cr and Ni. The corrosion rates, which ranged between 2.7 and 32.5 mpy, were calculated from both the one day and the one week weight losses. These corrosion rates indicated a relatively mild corrosion on the dissolver vessel. The welded coupons consistently had a higher corrosion rate than the non-welded coupons. The difference between the two decreased as the solution aggressiveness decreased. In these test solutions, aggressiveness corresponded with the fluoride concentration. Based on the results of this study, any corrosion occurring during the Mark 42 Campaign is not expected to have a deleterious effect on the dissolver vessel.

Mickalonis, J; Kerry Dunn, K

1999-08-01T23:59:59.000Z

295

The resistance of recent marine carbonate sediments to solution  

E-Print Network [OSTI]

H of the solution from about 8?0 at 1 week to 8. 2 at 10 weeks. C H A P T E R I V CONCLUSIONS The results of this study indicate: l. The grain size of recent marine carbonate sediments have ++ ++ no relationship to the amount of Ca or Mg dissolved... sediment samples ++ t3 Dissolved Mg from unground marine carbonate sediment samples C5 UJ o CO (0 C3 I. O 0. 8 0. 6 0. 4 ~E 0. 2 o. o 0 ~ ~ ai 0 ? ~ ? ~ 0 2 4 % MgCOp IN THE SAMPLE IO 12 C) Ld O U) C5 E I. O 0. 8 0. 6 0. 4...

Jansen, John F

1962-01-01T23:59:59.000Z

296

DISCOLORATION OF THE WETTED SURFACE IN THE 6.1D DISSOLVER  

SciTech Connect (OSTI)

During a camera inspection of a failed coil in the 6.1D dissolver, an orange discoloration was observed on a portion of the dissolver wall and coils. At the request of H-Canyon Engineering, the inspection video of the dissolver was reviewed by SRNL to assess if the observed condition (a non-uniform, orange-colored substance on internal surfaces) was a result of corrosion. Although the dissolver vessel and coil corrode during dissolution operations, the high acid conditions are not consistent with the formation of ferrous oxides (i.e., orange/rust-colored corrosion products). In a subsequent investigation, SRNL performed dissolution experiments to determine if residues from the nylon bags used for Pu containment could have generated the orange discoloration following dissolution. When small pieces of a nylon bag were placed in boiling 8 M nitric acid solutions containing other components representative of the H-Canyon process, complete dissolution occurred almost immediately. No residues were obtained even when a nylon mass to volume ratio greater than 100 times the 6.1D dissolver value was used. Degradation products from the dissolution of nylon bags are not responsible for the discoloration observed in the dissolver.

Rudisill, T.; Mickalonis, J.; Crapse, K.

2013-12-18T23:59:59.000Z

297

Carbon dynamics of terrestrial ecosystems on the Tibetan Plateau  

E-Print Network [OSTI]

RESEARCH PAPER Carbon dynamics of terrestrial ecosystems on the Tibetan Plateau during the 20th tundra to evergreen tropics. Its soils are dominated by permafrost and are rich in organic carbon. Its, the carbon dynamics of the Tibetan Plateau have not been well quantified under changes of climate and per

Xiao, Jingfeng

298

Wildland fire emissions, carbon, and climate: Emission factors Shawn Urbanski  

E-Print Network [OSTI]

Wildland fire emissions, carbon, and climate: Emission factors Shawn Urbanski Missoula Fire burning Greenhouse gases Emission factors a b s t r a c t While the vast majority of carbon emitted wildland fire greenhouse gas and aerosol (organic aerosol (OA) and black carbon (BC)) emission inventories

299

Method for making carbon films  

SciTech Connect (OSTI)

A method for treating an organic polymer material, preferably a vinylidene chloride/vinyl chloride copolymer (Saran) to produce a flat sheet of carbon film material having a high surface area ([approx equal]1000 m[sup 2] /g) suitable as an electrode material for super capacitor applications. The method comprises heating a vinylidene chloride/vinyl chloride copolymer film disposed between two spaced apart graphite or ceramic plates to a first temperature of about 160 C for about 14 hours to form a stabilized vinylidene chloride/vinyl chloride polymer film, thereafter heating the stabilized film to a second temperature of about 750 C in an inert atmosphere for about one hour to form a carbon film; and finally activating the carbon film to increase the surface area by heating the carbon film in an oxidizing atmosphere to a temperature of at least 750--850 C for between 1--6 hours. 2 figs.

Tan, M.X.

1999-07-29T23:59:59.000Z

300

PREDICTION OF TOTAL DISSOLVED GAS EXCHANGE AT HYDROPOWER DAMS  

SciTech Connect (OSTI)

Total dissolved gas (TDG) supersaturation in waters released at hydropower dams can cause gas bubble trauma in fisheries resulting in physical injuries and eyeball protrusion that can lead to mortality. Elevated TDG pressures in hydropower releases are generally caused by the entrainment of air in spillway releases and the subsequent exchange of atmospheric gasses into solution during passage through the stilling basin. The network of dams throughout the Columbia River Basin (CRB) are managed for irrigation, hydropower production, flood control, navigation, and fish passage that frequently result in both voluntary and involuntary spillway releases. These dam operations are constrained by state and federal water quality standards for TDG saturation which balance the benefits of spillway operations designed for Endangered Species Act (ESA)-listed fisheries versus the degradation to water quality as defined by TDG saturation. In the 1970s, the United States Environmental Protection Agency (USEPA), under the federal Clean Water Act (Section 303(d)), established a criterion not to exceed the TDG saturation level of 110% in order to protect freshwater and marine aquatic life. The states of Washington and Oregon have adopted special water quality standards for TDG saturation in the tailrace and forebays of hydropower facilities on the Columbia and Snake Rivers where spillway operations support fish passage objectives. The physical processes that affect TDG exchange at hydropower facilities have been studied throughout the CRB in site-specific studies and routine water quality monitoring programs. These data have been used to quantify the relationship between project operations, structural properties, and TDG exchange. These data have also been used to develop predictive models of TDG exchange to support real-time TDG management decisions. These empirically based predictive models have been developed for specific projects and account for both the fate of spillway and powerhouse flows in the tailrace channel and resultant exchange in route to the next downstream dam. Currently, there exists a need to summarize the general finding from operational and structural TDG abatement programs conducted throughout the CRB and for the development of a generalized prediction model that pools data collected at multiple projects with similar structural attributes. A generalized TDG exchange model can be tuned to specific projects and coupled with water regulation models to allow the formulation of optimal daily water regulation schedules subject to water quality constraints for TDG supersaturation. A generalized TDG exchange model can also be applied to other hydropower dams that affect TDG pressures in tailraces and can be used to develop alternative operational and structural measures to minimize TDG generation. It is proposed to develop a methodology for predicting TDG levels downstream of hydropower facilities with similar structural properties as a function of a set of variables that affect TDG exchange; such as tailwater depth, spill discharge and pattern, project head, and entrainment of powerhouse releases. TDG data from hydropower facilities located throughout the northwest region of the United States will be used to identify relationships between TDG exchange and relevant dependent variables. Data analysis and regression techniques will be used to develop predictive TDG exchange expressions for various structural categories.

Hadjerioua, Boualem [ORNL; Pasha, MD Fayzul K [ORNL; Stewart, Kevin M [ORNL; Bender, Merlynn [Bureau of Reclamation; Schneider, Michael L. [U.S. Army Corps of Engineers

2012-07-01T23:59:59.000Z

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


301

Low Carbon Fuel Standards  

E-Print Network [OSTI]

gas, or even coal with carbon capture and sequestration. Afuels that facilitate carbon capture and sequestration. Forenergy and could capture and sequester carbon emissions.

Sperling, Dan; Yeh, Sonia

2009-01-01T23:59:59.000Z

302

Carbon supercapacitors  

SciTech Connect (OSTI)

Carbon supercapacitors are represented as distributed RC networks with transmission line equivalent circuits. At low charge/discharge rates and low frequencies these networks approximate a simple series R{sub ESR}C circuit. The energy efficiency of the supercapacitor is limited by the voltage drop across the ESR. The pore structure of the carbon electrode defines the electrochemically active surface area which in turn establishes the volume specific capacitance of the carbon material. To date, the highest volume specific capacitance reported for a supercapacitor electrode is 220F/cm{sup 3} in aqueous H{sub 2}SO{sub 4} (10) and {approximately}60 F/cm{sup 3} in nonaqueous electrolyte (8).

Delnick, F.M.

1993-11-01T23:59:59.000Z

303

Summary of Tests to Determine Effectiveness of Gelatin Strike on SS{ampersand}C Dissolver Solutions  

SciTech Connect (OSTI)

The solutions from the dissolution of sand, slag, and crucible (SS&C) material are sufficiently different from previous solutions processed via the F-Canyon Purex process that the effectiveness of individual process steps needed to be ascertained. In this study, the effectiveness of gelatin strike was tested under a variety of conditions. Specifically, several concentrations of silica, fluoride, nitric acid (HNO{sub 3}), boric acid (H{sub 3}BO{sub 3}), and aluminium nitrate nonahydrate (ANN) were studied. The disengagement times of surrogate and plant SS&C dissolver solutions from plant solvent also were measured. The results of the tests indicate that gelatin strike does not coagulate the silica at the low concentration of silica ({tilde 30} ppm) expected in the SS&C dissolver solutions because the silicon is complexed with fluoride ions (e.g., SiF{sub 6}{sup -2}). The silicon fluoride complex is expected to remain with the aqueous phase during solvent extraction. The disengagement times of the dissolver solutions from the plant solvent were not affected by the presence of low concentrations of silica and no third phase formation was observed in the disengagement phase with the low silica concentrations. Tests of surrogate SS&C dissolver solutions with higher concentration of silica (less than 150 ppm) did show that gelatin strike followed by centrifugation resulted in good phase disengagement of the surrogate SS{ampersand}C dissolver solution from the plant dissolver solution. At the higher silica concentrations, there is not sufficient fluoride to complex with the silica, and the silica must be entrained by the gelatin and removed from the dissolver solution prior to solvent extraction.

Murray, A.M. [Westinghouse Savannah River Company, AIKEN, SC (United States); Karraker, D.G.

1998-05-01T23:59:59.000Z

304

Carbon microtubes  

DOE Patents [OSTI]

A carbon microtube comprising a hollow, substantially tubular structure having a porous wall, wherein the microtube has a diameter of from about 10 .mu.m to about 150 .mu.m, and a density of less than 20 mg/cm.sup.3. Also described is a carbon microtube, having a diameter of at least 10 .mu.m and comprising a hollow, substantially tubular structure having a porous wall, wherein the porous wall comprises a plurality of voids, said voids substantially parallel to the length of the microtube, and defined by an inner surface, an outer surface, and a shared surface separating two adjacent voids.

Peng, Huisheng (Shanghai, CN); Zhu, Yuntian Theodore (Cary, NC); Peterson, Dean E. (Los Alamos, NM); Jia, Quanxi (Los Alamos, NM)

2011-06-14T23:59:59.000Z

305

Surface-Initiated Titanium-Mediated Coordination Polymerization from Catalyst-Functionalized Single and Multiwalled Carbon Nanotubes  

SciTech Connect (OSTI)

Single (SWNTs) and multiwalled (MWNTs) carbon nanotubes were functionalized with a titanium alkoxide catalyst through a Diels-Alder cycloaddition reaction. The catalyst-functionalized carbon nanotubes (CNTs) were used for the surface initiated titanium-mediated coordination polymerizations of L-lactide (L-LA), -caprolactone (-CL) and n-hexyl isocyanate (HIC) employing the grafting from technique. 1H NMR, IR and Raman spectra showed that the precursor catalyst was successfully synthesized and covalently attached on the CNTs surface. Thermogravimetric analysis (TGA) revealed that the grafted poly(L-lactide) (PLLA) content could be controlled with time. The final polymer-grafted CNTs were readily dissolved in organic solvents as compared to the insoluble pristine and catalyst-functionalized CNTs. The presence of thick layers of polymers around the CNTs was observed through transmission electron microscopy (TEM). Differential scanning calorimetry (DSC) proved that the glass transition (Tg) and melting (Tm) temperatures of the PLLA are affected by the presence of the CNTs, while PLLA R-helix conformation remains intact, as revealed by the circular dichroism (CD) spectra.

Priftis, Dimitrios [ORNL; Petzetakis, Nikolaos [University of Athens, Athens, Greece; Sakellariou, Georgios [ORNL; Pitsikalis, Marinos [ORNL; Baskaran, Durairaj [University of Tennessee, Knoxville (UTK); Mays, Jimmy [ORNL; Hadjichristidis, Nikos [University of Athens, Athens, Greece

2009-01-01T23:59:59.000Z

306

Organic Matter Transformation in the Peat Column at Marcell Experimental Forest: Humification and Vertical Stratification  

SciTech Connect (OSTI)

A large-scale ecosystem manipulation (Spruce and Peatland Responses under Climatic and Environmental Change, SPRUCE) is being constructed in the Marcell Experimental Forest, Minnesota, USA, to determine the effects of climatic forcing on ecosystem processes in northern peatlands. Prior to the initiation of the manipulation, we characterized the solid-phase peat to a depth of 2 meters using a variety of techniques, including peat C:N ratios, 13C and 15N isotopic composition, Fourier Transform Infrared (FT IR), and 13C Nuclear Magnetic Resonance spectroscopy (13C NMR). FT IR determined peat humification-levels increased rapidly between and 75 cm, indicating a highly reactive zone. We observed a rapid drop in the abundance of O-alkyl-C, carboxyl-C, and other oxygenated functionalities within this zone and a concomitant increase in the abundance of alkyl- and nitrogen-containing compounds. Below 75-cm, minimal change was observed except that aromatic functionalities accumulated with depth. Incubation studies revealed the highest methane production rates and greatest CH4:CO2 ratios within this and 75 cm zone. Hydrology and surface vegetation played a role in belowground carbon cycling. Radiocarbon signatures of microbial respiration products in deeper porewaters resembled the signatures of dissolved organic carbon rather than solid phase peat, indicating that more recently photosynthesized organic matter fueled the bulk of subsurface microbial respiration. Oxygen-containing functionalities, especially O-alkyl-C, appear to serve as an excellent proxy for soil decomposition rate, and in addition should be a sensitive indicator of the response of the solid phase peat to the climatic manipulation.

Tfaily, Malak [Florida State University, Tallahassee; Cooper, Bill [Florida State University, Tallahassee; Kostka, [Georgia Institute of Technology, Atlanta; Chanton, Patrick R [ORNL; Schadt, Christopher Warren [ORNL; Hanson, Paul J [ORNL; Iversen, Colleen M [ORNL; Chanton, Jeff P [ORNL

2014-01-01T23:59:59.000Z

307

Analytical Chemistry Laboratory (ACL) procedure compendium. Volume 4, Organic methods  

SciTech Connect (OSTI)

This interim notice covers the following: extractable organic halides in solids, total organic halides, analysis by gas chromatography/Fourier transform-infrared spectroscopy, hexadecane extracts for volatile organic compounds, GC/MS analysis of VOCs, GC/MS analysis of methanol extracts of cryogenic vapor samples, screening of semivolatile organic extracts, GPC cleanup for semivolatiles, sample preparation for GC/MS for semi-VOCs, analysis for pesticides/PCBs by GC with electron capture detection, sample preparation for pesticides/PCBs in water and soil sediment, report preparation, Florisil column cleanup for pesticide/PCBs, silica gel and acid-base partition cleanup of samples for semi-VOCs, concentrate acid wash cleanup, carbon determination in solids using Coulometrics` CO{sub 2} coulometer, determination of total carbon/total organic carbon/total inorganic carbon in radioactive liquids/soils/sludges by hot persulfate method, analysis of solids for carbonates using Coulometrics` Model 5011 coulometer, and soxhlet extraction.

Not Available

1993-08-01T23:59:59.000Z

308

Rock Physics Characterization of Organic-Rich Shale Formations to Predict Organic Properties  

E-Print Network [OSTI]

rely on to assess the economic potential of these formations are: total organic carbon (TOC), thermal maturity, hydrocarbon saturation, porosity, mineralogy and brittleness. In this thesis, I investigate rock physics models and methods for the possible...

Bush, Brandon

2013-07-29T23:59:59.000Z

309

Frustrated Organic Solids Display Unexpected Gas Sorption  

SciTech Connect (OSTI)

Calixarene based organic solid can hold guests such as toluene and other organic molecules we have discovered a new type of material which believe involves a frustration of the solvate lattice as it moves toward the thermodynamically stable desolvated state. The intermediated phase with partial solvent content unexpectedly sorbs gases such as carbon dioxide and highly explosive acetylene deep inside the crystal lattice.

Thallapally, Praveen K.; Dalgarno, Scott J.; Atwood, Jerry L.

2006-11-27T23:59:59.000Z

310

In Situ Infrared Spectroscopic Study of Brucite Carbonation in Dry to Water-Saturated Supercritical Carbon Dioxide  

SciTech Connect (OSTI)

In geologic carbon sequestration, while part of the injected carbon dioxide will dissolve into host brine, some will remain as neat to water saturated super critical CO2 (scCO2) near the well bore and at the caprock, especially in the short-term life cycle of the sequestration site. Little is known about the reactivity of minerals with scCO2 containing variable concentrations of water. In this study, we used high-pressure infrared spectroscopy to examine the carbonation of brucite (Mg(OH)2) in situ over a 24 hr reaction period with scCO2 containing water concentrations between 0% and 100% saturation, at temperatures of 35, 50, and 70 °C, and at a pressure of 100 bar. Little or no detectable carbonation was observed when brucite was reacted with neat scCO2. Higher water concentrations and higher temperatures led to greater brucite carbonation rates and larger extents of conversion to magnesium carbonate products. The only observed carbonation product at 35 °C was nesquehonite (MgCO3 • 3H2O). Mixtures of nesquehonite and magnesite (MgCO3) were detected at 50 °C, but magnesite was more prevalent with increasing water concentration. Both an amorphous hydrated magnesium carbonate solid and magnesite were detected at 70 °C, but magnesite predominated with increasing water concentration. The identity of the magnesium carbonate products appears strongly linked to magnesium water exchange kinetics through temperature and water availability effects.

Loring, John S.; Thompson, Christopher J.; Zhang, Changyong; Wang, Zheming; Schaef, Herbert T.; Rosso, Kevin M.

2012-04-25T23:59:59.000Z

311

Carbon Storage Program  

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

Carbon Sequestration Partnership MSU . . . . . . . . . . . . . . . . . . . . . . . Montana State University MVA . . . . . . . . . . . . . . . . . . . . . . . Monitoring,...

312

LETTER doi:10.1038/nature10854 Uncovering the Neoproterozoic carbon cycle  

E-Print Network [OSTI]

Ccarb and d13 C in organic carbon (d13 Corg) will covary, offset by the fractionation impartedLETTER doi:10.1038/nature10854 Uncovering the Neoproterozoic carbon cycle D. T. Johnston1 , F. A events in Earth history are, in large part, derived from the stable carbon isotope records of carbonate

Schrag, Daniel

313

Oxidation and methylation of dissolved elemental mercury by anaerobic bacteria  

SciTech Connect (OSTI)

Methylmercury is a neurotoxin that poses significant health risks to humans. Some anaerobic sulphate- and iron-reducing bacteria can methylate oxidized forms of mercury, generating methylmercury1-4. One strain of sulphate-reducing bacteria (Desulfovibrio desulfuricans ND132) can also methylate elemental mercury5. The prevalence of this trait among different bacterial strains and species remains unclear, however. Here, we compare the ability of two strains of the sulphate-reducing bacterium Desulfovibrio and one strain of the iron-reducing bacterium Geobacter to oxidise and methylate elemental mercury in a series of laboratory incubations. Experiments were carried out under dark, anaerobic conditions, in the presence of environmentally-relevant concentrations of elemental mercury. We report differences in the ability of these organisms to oxidise and methylate elemental mercury. In line with recent findings5, we show that Desulfovibrio desulfuricans ND132 can both oxidise and methylate elemental mercury. However, the rate of methylation of elemental mercury is only about one third the rate of methylation of oxidized mercury. We also show that Desulfovibrio alaskensis G20 can oxidise, but not methylate, elemental mercury. Geobacter sulfurreducens PCA is able to oxidise and methylate elemental mercury in the presence of cysteine. We suggest that the activity of methylating and non-methylating bacteria may together enhance the formation of methylmercury in anaerobic environments.

Hu, Haiyan [ORNL] [ORNL; Lin, Hui [ORNL] [ORNL; Zheng, Wang [ORNL] [ORNL; Tomanicek, Stephen J [ORNL] [ORNL; Johs, Alexander [ORNL] [ORNL; Feng, Xinbin [ORNL] [ORNL; Elias, Dwayne A [ORNL] [ORNL; Liang, Liyuan [ORNL] [ORNL; Liang, Liyuan [ORNL] [ORNL; Gu, Baohua [ORNL] [ORNL

2013-01-01T23:59:59.000Z

314

Carbon Additionality: Discussion Paper  

E-Print Network [OSTI]

ahead, and identifying the carbon pools and other green house gas emissions sources and savings coveredCarbon Additionality: A review Discussion Paper Gregory Valatin November 2009 Forest Research. Voluntary Carbon Standards American Carbon Registry Forest Carbon Project Standard (ACRFCPS) 27 Carbon

315

On-line fast response device and method for measuring dissolved gas in a fluid  

DOE Patents [OSTI]

A method and device for the measurement of dissolved gas within a fluid. The fluid, substantially a liquid, is pumped into a pipe. The flow of the fluid is temporally restricted, creating one or more low pressure regions. A measurement indicative of trapped air is taken before and after the restriction. The amount of dissolved air is calculated from the difference between the first and second measurements. Preferably measurements indicative of trapped air is obtained from one or more pressure transducers, capacitance transducers, or combinations thereof. In the alternative, other methods such as those utilizing x-rays or gamma rays may also be used to detect trapped air. Preferably, the fluid is a hydraulic fluid, whereby dissolved air in the fluid is detected.

Tutu, Narinder Kumar (Manorville, NY)

2011-01-11T23:59:59.000Z

316

PREDICTION OF DISSOLVER LIFETIMES THROUGH NON-DESTRUCTIVE EVALUATION AND LABORATORY TESTING  

SciTech Connect (OSTI)

Non-destructive evaluation was used as the primary method of monitoring the corrosion degradation of nuclear material dissolvers and assessing the remaining lifetimes. Materials were typically processed in nitric acid based (4-14M) solutions containing fluoride concentrations less than 0.2 M. The primary corrosion issue for the stainless steel dissolvers is the occurrence of localized corrosion near the tank bottom and the heat affected zones of the welds. Laboratory data for a range of operational conditions, including solution chemistry and temperature, was used to assess the impact of processing changes on the dissolver corrosion rate. Experimental and NDE-based general corrosion rates were found to be in reasonable agreement for standard dissolution chemistries consisting of nitric acid with fluorides and at temperatures less than 95 C. Greater differences were observed when chloride was present as an impurity and temperatures exceeded 100 C.

Mickalonis, J.; Woodsmall, T.; Hinz, W.; Edwards, T.

2011-10-03T23:59:59.000Z

317

FLUIDIZED BED STEAM REFORMING (FBSR) OF HIGH LEVEL WASTE (HLW) ORGANIC AND NITRATE DESTRUCTION PRIOR TO VITRIFICATION: CRUCIBLE SCALE TO ENGINEERING SCALE DEMONSTRATIONS AND NON-RADIOACTIVE TO RADIOACTIVE DEMONSTRATIONS  

SciTech Connect (OSTI)

Over a decade ago, an in-tank precipitation process to remove Cs-137 from radioactive high level waste (HLW) supernates was demonstrated at the Savannah River Site (SRS). The full scale demonstration with actual HLW was performed in SRS Tank 48 (T48). Sodium tetraphenylborate (NaTPB) was added to enable Cs-137 extraction as CsTPB. The CsTPB, an organic, and its decomposition products proved to be problematic for subsequent processing of the Cs-137 precipitate in the SRS HLW vitrification facility for ultimate disposal in a HLW repository. Fluidized Bed Steam Reforming (FBSR) is being considered as a technology for destroying the organics and nitrates in the T48 waste to render it compatible with subsequent HLW vitrification. During FBSR processing the T48 waste is converted into organic-free and nitrate-free carbonate-based minerals which are water soluble. The soluble nature of the carbonate-based minerals allows them to be dissolved and pumped to the vitrification facility or returned to the tank farm for future vitrification. The initial use of the FBSR process for T48 waste was demonstrated with simulated waste in 2003 at the Savannah River National Laboratory (SRNL) using a specially designed sealed crucible test that reproduces the FBSR pyrolysis reactions, i.e. carbonate formation, organic and nitrate destruction. This was followed by pilot scale testing of simulants at the Science Applications International Corporation (SAIC) Science & Technology Application Research (STAR) Center in Idaho Falls, ID by Idaho National Laboratory (INL) and SRNL in 2003-4 and then engineering scale demonstrations by THOR{reg_sign} Treatment Technologies (TTT) and SRS/SRNL at the Hazen Research, Inc. (HRI) test facility in Golden, CO in 2006 and 2008. Radioactive sealed crucible testing with real T48 waste was performed at SRNL in 2008, and radioactive Benchscale Steam Reformer (BSR) testing was performed in the SRNL Shielded Cell Facility (SCF) in 2008.

Jantzen, C; Michael Williams, M; Gene Daniel, G; Paul Burket, P; Charles Crawford, C

2009-02-07T23:59:59.000Z

318

Selecting activated carbon for water and wastewater treatability studies  

SciTech Connect (OSTI)

A series of follow-up investigations were performed to produce data for improving the four-indicator carbon selection method that we developed to identify high-potential activated carbons effective for removing specific organic water pollutants. The carbon's pore structure and surface chemistry are dependent on the raw material and the activation process. Coconut carbons have relatively more small pores than large pores; coal and apricot nutshell/walnut shell fruit carbons have the desirable pore structures for removing adsorbates of all sizes. Chemical activation, excessive activation, and/or thermal reactivation enlarge small pores, resulting in reduced phenol number and higher tannic acid number. Activated carbon's phenol, iodine, methylene blue, and tannic acid numbers are convenient indicators of its surface area and pore volume of pore diameters < 10, 10-15, 15-28, and > 28 angstrom, respectively. The phenol number of a carbon is also a good indicator of its surface acidity of oxygen-containing organic functional groups that affect the adsorptive capacity for aromatic and other small polar organics. The tannic acid number is an indicator of carbon's capacity for large, high-molecular-weight natural organic precursors of disinfection by-products in water treatment. The experimental results for removing nitrobenzene, methyl-tert-butyl ether, 4,4-bisphenol, humic acid, and the organic constituents of a biologically treated coking-plant effluent have demonstrated the effectiveness of this capacity-indicator-based method of carbon selection.

Zhang, W.; Chang, Q.G.; Liu, W.D.; Li, B.J.; Jiang, W.X.; Fu, L.J.; Ying, W.C. [East China University of Chemical Technology, Shanghai (China)

2007-10-15T23:59:59.000Z

319

A literature review of actinide-carbonate mineral interactions  

SciTech Connect (OSTI)

Chemical retardation of actinides in groundwater systems is a potentially important mechanism for assessing the performance of the Waste Isolation Pilot Plant (WIPP), a facility intended to demonstrate safe disposal of transuranic waste. Rigorous estimation of chemical retardation during transport through the Culebra Dolomite, a water-bearing unit overlying the WIPP, requires a mechanistic understanding of chemical reactions between dissolved elements and mineral surfaces. This report represents a first step toward this goal by examining the literature for pertinent experimental studies of actinide-carbonate interactions. A summary of existing models is given, along with the types of experiments on which these models are based. Articles pertaining to research into actinide interactions with carbonate minerals are summarized. Select articles involving trace element-carbonate mineral interactions are also reviewed and may serve as templates for future research. A bibliography of related articles is included. Americium(III), and its nonradioactive analog neodymium(III), partition strongly from aqueous solutions into carbonate minerals. Recent thermodynamic, kinetic, and surface studies show that Nd is preferentially removed from solution, forming a Nd-Ca carbonate solid solution. Neptunium(V) is rapidly removed from solution by carbonates. Plutonium incorporation into carbonates is complicated by multiple oxidation states. Little research has been done on the radium(H) and thorium(IV) carbonate systems. Removal of uranyl ion from solution by calcite is limited to monolayer surface coverage.

Stout, D.L. [Missouri Univ., Columbia, MO (United States). Dept. of Geological Sciences; Carroll, S.A. [Lawrence Livermore National Lab., CA (United States)

1993-10-01T23:59:59.000Z

320

Understanding and engineering interfacial charge transfer of carbon nanotubes and graphene for energy and sensing applications  

E-Print Network [OSTI]

Graphene is a one-atom thick planar monolayer of sp2 -bonded carbon atoms organized in a hexagonal crystal lattice. A single walled carbon nanotube (SWCNT) can be thought of as a graphene sheet rolled up into a seamless ...

Paulus, Geraldine L. C. (Geraldine Laura Caroline)

2013-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


321

Carbon Trading, Carbon Taxes and Social Discounting  

E-Print Network [OSTI]

Carbon Trading, Carbon Taxes and Social Discounting Elisa Belfiori belf0018@umn.edu University of Minnesota Abstract This paper considers the optimal design of policies to carbon emissions in an economy, such as price or quantity controls on the net emissions of carbon, are insufficient to achieve the social

Weiblen, George D

322

Dissolution of Irradiated Commercial UO2 Fuels in Ammonium Carbonate and Hydrogen Peroxide  

SciTech Connect (OSTI)

We propose and test a disposition path for irradiated nuclear fuel using ammonium carbonate and hydrogen peroxide media. We demonstrate on a 13 g scale that >98% of the irradiated fuel dissolves. Subsequent expulsion of carbonate from the dissolver solution precipitates >95% of the plutonium, americium, curium, and substantial amounts of fission products, effectively partitioning the fuel at the dissolution step. Uranium can be easily recovered from solution by any of several means, such as ion exchange, solvent extraction, or direct precipitation. Ammonium carbonate can be evaporated from solution and recovered for re-use, leaving an extremely compact volume of fission products, transactinides, and uranium. Stack emissions are predicted to be less toxic, less radioactive, chemically simpler, and simpler to treat than those from the conventional PUREX process.

Soderquist, Chuck Z.; Johnsen, Amanda M.; McNamara, Bruce K.; Hanson, Brady D.; Chenault, Jeffrey W.; Carson, Katharine J.; Peper, Shane M.

2011-01-18T23:59:59.000Z

323

Investigation of the organic matter in inactive nuclear tank liquids  

SciTech Connect (OSTI)

Environmental Protection Agency (EPA) methodology for regulatory organics fails to account for the organic matter that is suggested by total organic carbon (TOC) analysis in the Oak Ridge National Laboratory (ORNL) inactive nuclear waste-tank liquids and sludges. Identification and measurement of the total organics are needed to select appropriate waste treatment technologies. An initial investigation was made of the nature of the organics in several waste-tank liquids. This report details the analysis of ORNL wastes.

Schenley, R.L.; Griest, W.H.

1990-08-01T23:59:59.000Z

324

Organic Superconductors  

SciTech Connect (OSTI)

Intense magnetic fields are an essential tool for understanding layered superconductors. Fundamental electronic properties of organic superconductors are revealed in intense (60 tesla) magnetic fields. Properties such as the topology of the Fermi surface and the nature of the superconducting order parameter are revealed. With modest maximum critical temperatures~13K the charge transfer salt organic superconductors prove to be incredibly valuable materials as their electronically clean nature and layered (highly anisotropic) structures yield insights to the high temperature superconductors. Observation of de Haas-van Alphen and Shubnikov-de Haas quantum oscillatory phenomena, magnetic field induced superconductivity and re-entrant superconductivity are some of the physical phenomena observed in the charge transfer organic superconductors. In this talk, I will discuss the nature of organic superconductors and give an overview of the generation of intense magnetic fields; from the 60 tesla millisecond duration to the extreme 1000 tesla microsecond pulsed magnetic fields.

Charles Mielke

2009-02-27T23:59:59.000Z

325

Chlorofluorocarbons, Sulfur Hexafluoride, and Dissolved Permanent Gases in Ground Water from Selected Sites In and Near the Idaho National Engineering and Environmental Laboratory, Idaho, 1994 - 1997  

SciTech Connect (OSTI)

From July 1994 through May 1997, the U.S. Geological Survey, in cooperations with the Department of Energy, sampled 86 wells completed in the Snake River Plain aquifer at and near the Idaho National Engineering and Environmental Laboratory (INEEL). The wells were sampled for a variety of constituents including one- and two-carbon halocarbons. Concentrations of dichlorodifluoromethane (CFC-12), trichlorofluoromethane (CFC-11), and trichlorotrifluororoethane (CFC-113) were determined. The data will be used to evaluate the ages of ground waters at INEEL. The ages of the ground water will be used to determine recharge rates, residence time, and travel time of water in the Snake River Plain aquifer in and near INEEL. The chromatograms of 139 ground waters are presented showing a large number of halomethanes, haloethanes, and haloethenes present in the ground waters underlying the INEEL. The chromatograms can be used to qualitatively evaluate a large number of contaminants at parts per trillion to parts per billion concentrations. The data can be used to study temporal and spatial distribution of contaminants in the Snake River Plain aquifer. Representative compressed chromatograms for all ground waters sampled in this study are available on two 3.5-inch high density computer disks. The data and the program required to decompress the data can be obtained from the U.S. Geological Survey office at Idaho Falls, Idaho. Sulfur hexafluoride (SF6) concentrations were measured in selected wells to determine the feasibility of using this environmental tracer as an age dating tool of ground water. Concentrations of dissolved nitrogen, argon, carbon dioxide, oxygen, and methane were measured in 79 ground waters. Concentrations of dissolved permanent gases are tabulated and will be used to evaluate the temperature of recharge of ground water in and near the INEEL.

Busenberg, E.; Plummer, L.N.; Bartholomay, R.C.; Wayland, J.E.

1998-08-01T23:59:59.000Z

326

On carbon footprints and growing energy use  

SciTech Connect (OSTI)

Could fractional reductions in the carbon footprint of a growing organization lead to a corresponding real reduction in atmospheric CO{sub 2} emissions in the next ten years? Curtis M. Oldenburg, head of the Geologic Carbon Sequestration Program of LBNL’s Earth Sciences Division, considers his own organization's carbon footprint and answers this critical question? In addressing the problem of energy-related greenhouse gas (GHG) emissions and climate change, it is essential that we understand which activities are producing GHGs and the scale of emission for each activity, so that reduction efforts can be efficiently targeted. The GHG emissions to the atmosphere of an individual or group are referred to as the ‘carbon footprint’. This terminology is entirely appropriate, because 85% of the global marketed energy supply comes from carbon-rich fossil fuel sources whose combustion produces CO{sub 2}, the main GHG causing global climate change. Furthermore, the direct relation between CO2 emissions and fossil fuels as they are used today makes energy consumption a useful proxy for carbon footprint. It would seem to be a simple matter to reduce energy consumption across the board, both individually and collectively, to help reduce our carbon footprints and therefore solve the energyclimate crisis. But just how much can we reduce carbon footprints when broader forces, such as growth in energy use, cause the total footprint to simultaneously expand? In this feature, I present a calculation of the carbon footprint of the Earth Sciences Division (ESD), the division in which I work at Lawrence Berkeley National Laboratory (LBNL), and discuss the potential for reducing this carbon footprint. It will be apparent that in terms of potential future carbon footprint reductions under projections of expected growth, ESD may be thought of as a microcosm of the situation of the world as a whole, in which alternatives to the business-as-usual use of fossil fuels are needed if absolute GHG emission reductions are to be achieved.

Oldenburg, C.M.

2011-06-01T23:59:59.000Z

327

Public Review Draft: A Method for Assessing Carbon Stocks, Carbon  

E-Print Network [OSTI]

Public Review Draft: A Method for Assessing Carbon Stocks, Carbon Sequestration, and Greenhouse, and Zhu, Zhiliang, 2010, Public review draft; A method for assessing carbon stocks, carbon sequestration

328

Carbon-Optimal and Carbon-Neutral Supply Chains  

E-Print Network [OSTI]

Li, M. Daskin. 2009. Carbon Footprint and the Management ofThe Importance of Carbon Footprint Estimation Boundaries.Carbon accounting and carbon footprint - more than just

Caro, F.; Corbett, C. J.; Tan, T.; Zuidwijk, R.

2011-01-01T23:59:59.000Z

329

Method of dissolving metal oxides with di- or polyphosphonic acid and a redundant  

DOE Patents [OSTI]

A method of dissolving metal oxides using a mixture of a di- or polyphosphonic acid and a reductant wherein each is present in a sufficient amount to provide a synergistic effect with respect to the dissolution of metal oxides and optionally containing corrosion inhibitors and pH adjusting agents.

Horwitz, Earl P. (Argonne, IL); Chiarizia, Renato (Argonne, IL)

1996-01-01T23:59:59.000Z

330

Wastewater Discharge, Nutrient Loading, and Dissolved Oxygen Dynamics in a Shallow Texas Bay  

E-Print Network [OSTI]

In Oso Bay, a wastewater treatment plant acts as a source of eutrophication and may have measureable impact on the health of the bay. The objectives of this study were to create a model for modeling dissolved oxygen concentrations over time...

Schroer, Lee Allen

2014-05-07T23:59:59.000Z

331

Quantitative concentration measurements of creatinine dissolved in water and urine using Raman  

E-Print Network [OSTI]

to the lack of suitable materials with refractive indices lower that of water (n 1.33). Recently, howeverQuantitative concentration measurements of creatinine dissolved in water and urine using Raman in water and in urine. At short integration times, where shot noise is most troublesome, the enhanced

Berger, Andrew J.

332

Geographic variation in phenotypic plasticity in response to dissolved oxygen in an African cichlid fish  

E-Print Network [OSTI]

Geographic variation in phenotypic plasticity in response to dissolved oxygen in an African cichlid variation in a population over a number of generations to result in a population that is locally adapted and plastic variation in gill and brain size among swamp (low oxygen; hypoxic) and river (normal oxygen

Nuismer, Scott L.

333

Did BP's oil-dissolving chemical make the spill By Kate Spinner  

E-Print Network [OSTI]

Did BP's oil-dissolving chemical make the spill worse? By Kate Spinner Published: Monday, May 30, 2011 at 8:47 p.m. BP succeeded in sinking the oil from its blown well out of sight -- and keeping much chemicals. But the impact on the ecosystem as a whole may have been more damaging than the oil alone

Belogay, Eugene A.

334

Modeling transport of dissolved silica in a forested headwater catchment: Implications for defining the hydrochemical  

E-Print Network [OSTI]

in groundwater to be related to the saturation deficit in this zone. A positive correlation between the average and have emphasized the need for a rational, nonempirical approach for the identification stream water chemistry can provide valuable insight into the transport of dissolved materials

Scanlon, Todd

335

Changes in seal capacity of fractured claystone caprocks induced by dissolved and gaseous CO2 seepage  

E-Print Network [OSTI]

Changes in seal capacity of fractured claystone caprocks induced by dissolved and gaseous CO2; accepted 17 June 2008; published 31 July 2008. [1] Claystone caprocks are often the ultimate seal for CO2 underground storage when residual CO2 gas reaches the reservoir top due to buoyancy. Permeability changes

Luquot, Linda

336

Dissolved oxygen and pH monitoring within cell culture media using a hydrogel microarray sensor  

E-Print Network [OSTI]

and control of cell culture processes is required. To do this measurement, multiple sensors must be implemented to monitor various parameters of the cell culture medium. The model analytes used in this study were pH and dissolved oxygen which have...

Lee, Seung Joon

2009-05-15T23:59:59.000Z

337

Fate of Acids in Clouds 1. Combination with bases dissolved in clouds: acids neutralized  

E-Print Network [OSTI]

problems. E#11;ects of Acid Rain 1. Vegetation: SO 2 is toxic to plants #15; Leaves damaged below pH 3 rain { Athens and Rome cathedrals and statues: pollution leads to acid rain #15; SteelFate of Acids in Clouds 1. Combination with bases dissolved in clouds: acids neutralized NH 3 (g

Schofield, Jeremy

338

Preferential Solvent Partitioning within Asphaltenic Aggregates Dissolved in Binary Solvent Mixtures  

E-Print Network [OSTI]

Preferential Solvent Partitioning within Asphaltenic Aggregates Dissolved in Binary SolventVised Manuscript ReceiVed December 9, 2006 The heaviest fraction of crude oils, asphaltenes, has been shown to play-assembled interfacially active asphaltenic aggregates. Thus, careful characterization of these aggregates is of great

Kilpatrick, Peter K.

339

Dissolved metal contamination in the East RiverLong Island sound system: potential biological effects  

E-Print Network [OSTI]

in the United States. The ER­WLIS region receives treated sewage from 18 wastewater treatment plants in New YorkDissolved metal contamination in the East River­Long Island sound system: potential biological sewage, and to assess its possible biological impact on local waters. The East River­Long Island Sound

Johnsen, Sönke

340

Observations of chromophoric dissolved and detrital organic matter distribution using remote sensing in the Southern Ocean: Validation, dynamics and regulation  

E-Print Network [OSTI]

is related to its role attenuating solar radiation and affecting ocean color algorithms (Siegel et al., 2002 CDOM dynamics. First, the Southern Ocean is subject to extreme solar radiation in the austral summer sensing in the Southern Ocean: Validation, dynamics and regulation E. Ortega-Retuerta a,b, , D.A. Siegel c

Siegel, David A.

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


341

The effect of surface irradiance on the absorption spectrum of chromophoric dissolved organic matter in the global ocean  

E-Print Network [OSTI]

.2 mm), is responsible for nearly 90% of ultraviolet (UV) radiation attenuation in the global ocean matter in the global ocean Chantal M. Swan a,n , Norman B. Nelson a , David A. Siegel a,b , Tihomir S to better assess the impact of CDOM on surface ocean photochemistry and remote sensing of ocean color

Siegel, David A.

342

Supplementary information1 S1: Estimation of the dissolved organic mass (DOM) concentrations in aqueous solutions3  

E-Print Network [OSTI]

(1). APCI-MS measurements of aqueous solutions by direct47 infusion of liquid solutions-MS measurements of aqueous solutions by direct47 infusion of liquid solutions, in the negative mode (a

Meskhidze, Nicholas

343

An empirical ocean color algorithm for estimating the contribution of chromophoric dissolved organic matter to total light absorption in  

E-Print Network [OSTI]

.14. As exemplified with the data from the Baltic and North Seas, the algorithm provides a means to distinguish depressing the water-leaving radiance recorded by remote sensing sensors [Carder et al., 1991]. [3

Babin, Marcel

344

Autonomous observations of the ocean biological carbon pump  

SciTech Connect (OSTI)

Prediction of the substantial biologically mediated carbon flows in a rapidly changing and acidifying ocean requires model simulations informed by observations of key carbon cycle processes on the appropriate space and time scales. From 2000 to 2004, the National Oceanographic Partnership Program (NOPP) supported the development of the first low-cost fully-autonomous ocean profiling Carbon Explorers that demonstrated that year-round real-time observations of particulate organic carbon (POC) concentration and sedimentation could be achieved in the world's ocean. NOPP also initiated the development of a sensor for particulate inorganic carbon (PIC) suitable for operational deployment across all oceanographic platforms. As a result, PIC profile characterization that once required shipboard sample collection and shipboard or shore based laboratory analysis, is now possible to full ocean depth in real time using a 0.2W sensor operating at 24 Hz. NOPP developments further spawned US DOE support to develop the Carbon Flux Explorer, a free-vehicle capable of following hourly variations of particulate inorganic and organic carbon sedimentation from near surface to kilometer depths for seasons to years and capable of relaying contemporaneous observations via satellite. We have demonstrated the feasibility of real time - low cost carbon observations which are of fundamental value to carbon prediction and when further developed, will lead to a fully enhanced global carbon observatory capable of real time assessment of the ocean carbon sink, a needed constraint for assessment of carbon management policies on a global scale.

Bishop, James K.B.

2009-03-01T23:59:59.000Z

345

Unsteady-state material balance model for a continuous rotary dissolver  

SciTech Connect (OSTI)

The unsteady-state continuous rotary dissolver material balance code (USSCRD) is a useful tool with which to study the performance of the rotary dissolver under a wide variety of operating conditions. The code does stepwise continuous material balance calculations around each dissolver stage and the digester tanks. Output from the code consists of plots and tabular information on the stagewise concentration profiles of UO{sub 2}, PuO{sub 2}, fission products, Pu(NO{sub 3}){sub 4}, UO{sub 2}(NO{sub 3}){sub 2}, fission product nitrates, HNO{sub 3}, H{sub 2}O, stainless steel, total particulate, and total fuel in pins. Other information about material transfers, stagewise liquid volume, material inventory, and dissolution performance is also provided. This report describes the development of the code, its limitations, key operating parameters, usage procedures, and the results of the analysis of several sets of operating conditions. Of primary importance in this work was the estimation of the steady-state heavy metal inventory in a 0.5-t/d dissolver drum. Values ranging from {similar_to}12 to >150 kg of U + Pu were obtained for a variety of operating conditions. Realistically, inventories are expected to be near the lower end of this range. Study of the variation of operating parameters showed significant effects on dissolver product composition from intermittent solids feed. Other observations indicated that the cycle times for the digesters and shear feed should be closely coupled in order to avoid potential problems with off-specification product. 19 references, 14 tables.

Lewis, B.E.

1984-09-01T23:59:59.000Z

346

Compacted carbon for electrochemical cells  

DOE Patents [OSTI]

This invention provides compacted carbon that is useful in the electrode of an alkali metal/carbon electrochemical cell of improved capacity selected from the group consisting of: (a) coke having the following properties: (1) an x-ray density of at least 2.00 grams per cubic centimeters, (2) a closed porosity of no greater than 5%, and (3) an open porosity of no greater than 47%; and (b) graphite having the following properties: (1) an x-ray density of at least 2.20 grams per cubic centimeters, (2) a closed porosity of no greater than 5%, and (3) an open porosity of no greater than 25%. This invention also relates to an electrode for an alkali metal/carbon electrochemical cell comprising compacted carbon as described above and a binder. This invention further provides an alkali metal/carbon electrochemical cell comprising: (a) an electrode as described above, (b) a non-aqueous electrolytic solution comprising an organic aprotic solvent and an electrolytically conductive salt and an alkali metal, and (c) a counter electrode. 10 figs.

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

1997-10-14T23:59:59.000Z

347

Terrestrial Carbon Management Data from the Carbon Dioxide Information Analysis Center (CDIAC)  

DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

CDIAC products are indexed and searchable through a customized interface powered by ORNL's Mercury search engine. Products include numeric data packages, publications, trend data, atlases, and models and can be searched for by subject area, keywords, authors, product numbers, time periods, collection sites, spatial references, etc. Some of the collections may also be included in the CDIAC publication Trends Online: A Compendium of Global Change Data. Most data sets, many with numerous data files, are free to download from CDIAC's ftp area. Collections under the broad heading of Terrestrial Carbon Management are organized as Carbon Accumulation with Cropland Management, Carbon Accumulation with Grassland Management, Carbon Loss Following Cultivation, Carbon Accumulation Following Afforestation, and Carbon Sources and Sinks Associated with U.S. Cropland Production.

348

Mongolia-Economics of Climate Change and Low Carbon Growth Strategies...  

Open Energy Info (EERE)

Name Mongolia-Economics of Climate Change and Low Carbon Growth Strategies in Northeast Asia AgencyCompany Organization Asian Development Bank Partner Government of Republic of...

349

Vietnam-Rapid Assessment of City Emissions (RACE) for Low Carbon...  

Open Energy Info (EERE)

Assessment of City Emissions (RACE) for Low Carbon Cities: Transport and Building Electricity Use AgencyCompany Organization Clean Air Asia, Chreod Ltd. Partner Asian...

350

E-Print Network 3.0 - affects marine carbon Sample Search Results  

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

the organic carbon content of marine aerosols... . Potential impact of ocean ecosystem changes due to global warming on marine341 ... Source: Russell, Lynn - Scripps...

351

Photophysics of carbon nanotubes  

E-Print Network [OSTI]

This thesis reviews the recent advances made in optical studies of single-wall carbon nanotubes. Studying the electronic and vibrational properties of carbon nanotubes, we find that carbon nanotubes less than 1 nm in ...

Samsonidze, Georgii G

2007-01-01T23:59:59.000Z

352

CALIFORNIA CARBON SEQUESTRATION THROUGH  

E-Print Network [OSTI]

CALIFORNIA ENERGY COMMISSION CARBON SEQUESTRATION THROUGH CHANGES IN LAND USE IN WASHINGTON. Carbon Sequestration Through Changes in Land Use in Washington: Costs and Opportunities. California for Terrestrial Carbon Sequestration in Oregon. Report to Winrock International. #12;ii #12;iii Preface

353

Carbon dioxide and climate  

SciTech Connect (OSTI)

Scientific and public interest in greenhouse gases, climate warming, and global change virtually exploded in 1988. The Department's focused research on atmospheric CO{sub 2} contributed sound and timely scientific information to the many questions produced by the groundswell of interest and concern. Research projects summarized in this document provided the data base that made timely responses possible, and the contributions from participating scientists are genuinely appreciated. In the past year, the core CO{sub 2} research has continued to improve the scientific knowledge needed to project future atmospheric CO{sub 2} concentrations, to estimate climate sensitivity, and to assess the responses of vegetation to rising concentrations of CO{sub 2} and to climate change. The Carbon Dioxide Research Program's goal is to develop sound scientific information for policy formulation and governmental action in response to changes of atmospheric CO{sub 2}. The Program Summary describes projects funded by the Carbon Dioxide Research Program during FY 1990 and gives a brief overview of objectives, organization, and accomplishments.

Not Available

1990-10-01T23:59:59.000Z

354

Method for catalytic destruction of organic materials  

DOE Patents [OSTI]

A method is disclosed for converting waste organic materials into an innocuous product gas. The method comprises maintaining, in a pressure vessel, in the absence of oxygen, at a temperature of 250.degree. C. to 500.degree. C. and a pressure of at least 50 atmospheres, a fluid organic waste material, water, and a catalyst consisting essentially of reduced nickel in an amount sufficient to catalyze a reaction of the organic waste material to produce an innocuous product gas composed primarily of methane and carbon dioxide. The methane in the product gas may be burned to preheat the organic materials.

Sealock, Jr., L. John (Richland, WA); Baker, Eddie G. (Richland, WA); Elliott, Douglas C. (Richland, WA)

1997-01-01T23:59:59.000Z

355

Method for catalytic destruction of organic materials  

DOE Patents [OSTI]

A method is disclosed for converting waste organic materials into an innocuous product gas. The method comprises maintaining, in a pressure vessel, in the absence of oxygen, at a temperature of 250 to 500 C and a pressure of at least 50 atmospheres, a fluid organic waste material, water, and a catalyst consisting essentially of reduced nickel in an amount sufficient to catalyze a reaction of the organic waste material to produce an innocuous product gas composed primarily of methane and carbon dioxide. The methane in the product gas may be burned to preheat the organic materials. 7 figs.

Sealock, L.J. Jr.; Baker, E.G.; Elliott, D.C.

1997-05-20T23:59:59.000Z

356

Method of making carbon-carbon composites  

DOE Patents [OSTI]

A process for making 2D and 3D carbon-carbon composites having a combined high crystallinity, high strength, high modulus and high thermal and electrical conductivity. High-modulus/high-strength mesophase derived carbon fibers are woven into a suitable cloth. Layers of this easily graphitizible woven cloth are infiltrated with carbon material to form green composites. The carbonized composite is then impregnated several times with pitch by covering the composite with hot pitch under pressure. The composites are given a heat treatment between each impregnant step to crack up the infiltrated carbon and allow additional pitch to enter the microstructure during the next impregnation cycle. The impregnated composites are then given a final heat treatment in the range 2500.degree. to 3100.degree. C. to fully graphitize the fibers and the matrix carbon. The composites are then infiltrated with pyrolytic carbon by chemical vapor deposition in the range 1000.degree. C. to 1300.degree. C. at a reduced. pressure.

Engle, Glen B. (16716 Martincoit Rd., Poway, CA 92064)

1993-01-01T23:59:59.000Z

357

Toward Zero Carbon Energy Production Toward Zero Carbon Energy Production  

E-Print Network [OSTI]

#12;Toward Zero Carbon Energy Production Toward Zero Carbon Energy Production Toward Zero Carbon Energy Production Toward Zero Carbon Energy Production Toward Zero Carbon Energy Production Toward Zero Carbon Energy Production Toward Zero Carbon Energy Production Toward Zero Carbon Energy Production Toward

Narasayya, Vivek

358

Carbon Code Requirements for voluntary carbon sequestration projects  

E-Print Network [OSTI]

Woodland Carbon Code Requirements for voluntary carbon sequestration projects ® Version 1.2 July trademark 10 3. Carbon sequestration 11 3.1 Units of carbon calculation 11 3.2 Carbon baseline 11 3.3 Carbon leakage 12 3.4 Project carbon sequestration 12 3.5 Net carbon sequestration 13 4. Environmental quality 14

359

Low Carbon Fuel Standards  

E-Print Network [OSTI]

in 1990. These many alternative-fuel initiatives failed tolow-cost, low-carbon alternative fuels would thrive. Theto introduce low-carbon alternative fuels. Former Federal

Sperling, Dan; Yeh, Sonia

2009-01-01T23:59:59.000Z

360

Carbon Capture (Carbon Cycle 2.0)  

ScienceCinema (OSTI)

Berend Smit speaks at the Carbon Cycle 2.0 kick-off symposium Feb. 3, 2010. We emit more carbon into the atmosphere than natural processes are able to remove - an imbalance with negative consequences. Carbon Cycle 2.0 is a Berkeley Lab initiative to provide the science needed to restore this balance by integrating the Labs diverse research activities and delivering creative solutions toward a carbon-neutral energy future. http://carboncycle2.lbl.gov/

Smit, Berend

2011-06-08T23:59:59.000Z

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


361

Long-term effects of soil warming on labile carbon availability and microbial community respiration and composition  

E-Print Network [OSTI]

of a positive feedback loop if this carbon were to enter the atmosphere. Much of the carbon that entersLong-term effects of soil warming on labile carbon availability and microbial community respiration of warming on the microbial community and soil organic carbon pool. Soils were incubated at various

Vallino, Joseph J.

362

Energy Carrier Transport In Surface-Modified Carbon Nanotubes  

E-Print Network [OSTI]

of organic molecules or inorganic nanoparticles, debundling of nanotubes by dispersing agents, and microwave irradiation. Because carbon nanotubes have unique carrier transport characteristics along a sheet of graphite in a cylindrical shape, the properties...

Ryu, Yeontack

2012-11-30T23:59:59.000Z

363

Composite carbon foam electrode  

DOE Patents [OSTI]

Carbon aerogels used as a binder for granularized materials, including other forms of carbon and metal additives, are cast onto carbon or metal fiber substrates to form composite carbon thin film sheets. The thin film sheets are utilized in electrochemical energy storage applications, such as electrochemical double layer capacitors (aerocapacitors), lithium based battery insertion electrodes, fuel cell electrodes, and electrocapacitive deionization electrodes. The composite carbon foam may be formed by prior known processes, but with the solid particles being added during the liquid phase of the process, i.e. prior to gelation. The other forms of carbon may include carbon microspheres, carbon powder, carbon aerogel powder or particles, graphite carbons. Metal and/or carbon fibers may be added for increased conductivity. The choice of materials and fibers will depend on the electrolyte used and the relative trade off of system resistivty and power to system energy.

Mayer, Steven T. (San Leandro, CA); Pekala, Richard W. (Pleasant Hill, CA); Kaschmitter, James L. (Pleasanton, CA)

1997-01-01T23:59:59.000Z

364

Composite carbon foam electrode  

DOE Patents [OSTI]

Carbon aerogels used as a binder for granulated materials, including other forms of carbon and metal additives, are cast onto carbon or metal fiber substrates to form composite carbon thin film sheets. The thin film sheets are utilized in electrochemical energy storage applications, such as electrochemical double layer capacitors (aerocapacitors), lithium based battery insertion electrodes, fuel cell electrodes, and electrocapacitive deionization electrodes. The composite carbon foam may be formed by prior known processes, but with the solid particles being added during the liquid phase of the process, i.e. prior to gelation. The other forms of carbon may include carbon microspheres, carbon powder, carbon aerogel powder or particles, graphite carbons. Metal and/or carbon fibers may be added for increased conductivity. The choice of materials and fibers will depend on the electrolyte used and the relative trade off of system resistivity and power to system energy. 1 fig.

Mayer, S.T.; Pekala, R.W.; Kaschmitter, J.L.

1997-05-06T23:59:59.000Z

365

Evaluation of filter media for clarification of partially dissolved residues containing plutonium  

SciTech Connect (OSTI)

A common process in the chemical industry employs the leaching of a desirable component from an insoluble substrate, followed by filtration to produce a clarified solution of the desirable component and a discardable residue. The work described here involved evaluating sintered metal filter media for separating dissolved plutonium from undissolved residues generated at various locations owned by the Department of Energy throughout the United States. The work was performed during a six-week assignment at the Savannah River Laboratory as part of a high school science enrichment program conducted in the summer of 1989. The leach step used included dissolving the plutonium-containing solids in a solution of nitric-hydrofluoric acid. To simulate the partial solubility of the actual plutonium-containing residues, a non-radioactive power plant flyash was used. 6 refs., 14 figs., 1 tab.

Foley, E.S.

1989-10-09T23:59:59.000Z

366

Ambient dissolved oxygen concentrations in Delaware's Inland Bays. Final report, June 6, 1984  

SciTech Connect (OSTI)

Ambient dissolved oxygen concentrations were measured at dawn during August, 1983, in Rehoboth and Indian River Bays. In Indian River Bay, 59% of the D.O. measurements were below the State minimum water quality standard of 5 mg L/sup -1/, while in Rehoboth Bay 17% of the values fail to meet the State standards. Diurnal dissolved oxygen curves measured at 5 stations in the Bays and tributary creeks, provide evidence that, although the Bays are in reasonable balance with respect to apparent net daytime photosynthesis (Pa) and nighttime respiration (Rn), the absolute values of Pa and Rn are very high, compared with other coastal ecosystems, except for central Rehoboth Bay. These conclusions are consistent with the annual nutrient loads to the systems, which are about double for Indian River when contrasted with Rehoboth. 11 references, 1 figure, 7 tables.

Biggs, R.B.

1984-01-01T23:59:59.000Z

367

FLOWSHEET EVALUATION FOR THE DISSOLVING AND NEUTRALIZATION OF SODIUM REACTOR EXPERIMENT USED NUCLEAR FUEL  

SciTech Connect (OSTI)

This report includes the literature review, hydrogen off-gas calculations, and hydrogen generation tests to determine that H-Canyon can safely dissolve the Sodium Reactor Experiment (SRE; thorium fuel), Ford Nuclear Reactor (FNR; aluminum alloy fuel), and Denmark Reactor (DR-3; silicide fuel, aluminum alloy fuel, and aluminum oxide fuel) assemblies in the L-Bundles with respect to the hydrogen levels in the projected peak off-gas rates. This is provided that the number of L-Bundles charged to the dissolver is controlled. Examination of SRE dissolution for potential issues has aided in predicting the optimal batching scenario. The calculations detailed in this report demonstrate that the FNR, SRE, and DR-3 used nuclear fuel (UNF) are bounded by MURR UNF and may be charged using the controls outlined for MURR dissolution in a prior report.

Daniel, W. E.; Hansen, E. K.; Shehee, T. C.

2012-10-30T23:59:59.000Z

368

Shallow Carbon Sequestration Demonstration Project  

SciTech Connect (OSTI)

The potential for carbon sequestration at relatively shallow depths was investigated at four power plant sites in Missouri. Exploratory boreholes were cored through the Davis Shale confining layer into the St. Francois aquifer (Lamotte Sandstone and Bonneterre Formation). Precambrian basement contact ranged from 654.4 meters at the John Twitty Energy Center in Southwest Missouri to over 1100 meters near the Sioux Power Plant in St. Charles County. Investigations at the John Twitty Energy Center included 3D seismic reflection surveys, downhole geophysical logging and pressure testing, and laboratory analysis of rock core and water samples. Plans to perform injectivity tests at the John Twitty Energy Center, using food grade CO{sub 2}, had to be abandoned when the isolated aquifer was found to have very low dissolved solids content. Investigations at the Sioux Plant and Thomas Hill Energy Center in Randolph County found suitably saline conditions in the St. Francois. A fourth borehole in Platte County was discontinued before reaching the aquifer. Laboratory analyses of rock core and water samples indicate that the St. Charles and Randolph County sites could have storage potentials worthy of further study. The report suggests additional Missouri areas for further investigation as well.

Pendergrass, Gary; Fraley, David; Alter, William; Bodenhamer, Steven

2013-09-30T23:59:59.000Z

369

Porous Metal-Organic Frameworks for Energy Storage Applications: Design, Synthesis and Mechanism Studies  

E-Print Network [OSTI]

The self-assembly of metal ions and organic linkers could afford 3-dimensional (3D) porous metal-organic frameworks (MOFs). They are promising materials for clean energy applications including carbon capture, hydrogen storage and methane storage...

Liu, Yangyang

2014-05-05T23:59:59.000Z

370

Vitrification of organics-containing wastes  

DOE Patents [OSTI]

A process for stabilizing organics-containing waste materials and recovery metals therefrom, and a waste glass product made according to the process are described. Vitrification of wastes such as organic ion exchange resins, electronic components and the like can be accomplished by mixing at least one transition metal oxide with the wastes, and, if needed, glass formers to compensate for a shortage of silicates or other glass formers in the wastes. The transition metal oxide increases the rate of oxidation of organic materials in the wastes to improve the composition of the glass-forming mixture: at low temperatures, the oxide catalyzes oxidation of a portion of the organics in the waste; at higher temperatures, the oxide dissolves and the resulting oxygen ions oxidize more of the organics; and at vitrification temperatures, the metal ions conduct oxygen into the melt to oxidize the remaining organics. In addition, the transition metal oxide buffers the redox potential of the glass melt so that metals such as Au, Pt, Ag, and Cu separate form the melt in the metallic state and can be recovered. After the metals are recovered, the remainder of the melt is allowed to cool and may subsequently be disposed of. The product has good leaching resistance and can be disposed of in an ordinary landfill, or, alternatively, used as a filler in materials such as concrete, asphalt, brick and tile.

Bickford, D.F.

1995-01-01T23:59:59.000Z

371

Vitrification of organics-containing wastes  

DOE Patents [OSTI]

A process is described for stabilizing organics-containing waste materials and recovering metals therefrom, and a waste glass product made according to the process is also disclosed. Vitrification of wastes such as organic ion exchange resins, electronic components and the like can be accomplished by mixing at least one transition metal oxide with the wastes, and, if needed, glass formers to compensate for a shortage of silicates or other glass formers in the wastes. The transition metal oxide increases the rate of oxidation of organic materials in the wastes to improve the composition of the glass-forming mixture: at low temperatures, the oxide catalyzes oxidation of a portion of the organics in the waste; at higher temperatures, the oxide dissolves and the resulting oxygen ions oxidize more of the organics; and at vitrification temperatures, the metal ions conduct oxygen into the melt to oxidize the remaining organics. In addition, the transition metal oxide buffers the redox potential of the glass melt so that metals such as Au, Pt, Ag, and Cu separate from the melt in the metallic state and can be recovered. After the metals are recovered, the remainder of the melt is allowed to cool and may subsequently be disposed of. The product has good leaching resistance and can be disposed of in an ordinary landfill, or, alternatively, used as a filler in materials such as concrete, asphalt, brick and tile. 1 fig.

Bickford, D.F.

1997-09-02T23:59:59.000Z

372

Vitrification of organics-containing wastes  

DOE Patents [OSTI]

A process for stabilizing organics-containing waste materials and recovering metals therefrom, and a waste glass product made according to the process. Vitrification of wastes such as organic ion exchange resins, electronic components and the like can be accomplished by mixing at least one transition metal oxide with the wastes, and, if needed, glass formers to compensate for a shortage of silicates or other glass formers in the wastes. The transition metal oxide increases the rate of oxidation of organic materials in the wastes to improve the composition of the glass-forming mixture: at low temperatures, the oxide catalyzes oxidation of a portion of the organics in the waste; at higher temperatures, the oxide dissolves and the resulting oxygen ions oxidize more of the organics; and at vitrification temperatures, the metal ions conduct oxygen into the melt to oxidize the remaining organics. In addition, the transition metal oxide buffers the redox potential of the glass melt so that metals such as Au, Pt, Ag, and Cu separate from the melt in the metallic state and can be recovered. After the metals are recovered, the remainder of the melt is allowed to cool and may subsequently be disposed of. The product has good leaching resistance and can be disposed of in an ordinary landfill, or, alternatively, used as a filler in materials such as concrete, asphalt, brick and tile.

Bickford, Dennis F. (Aiken, SC)

1997-01-01T23:59:59.000Z

373

Carbon aerogels: An update on structure, properties, and applications  

SciTech Connect (OSTI)

Aerogels are unique porous materials whose composition, structure, and properties can be controlled at the nanometer scale. This paper examines the synthesis of organic aerogels and their carbonized derivatives. Carbon aerogels have low electrical resistivity, high surface area, and a tunable pore size. These materials are finding applications as electrodes in double layer capacitors.

Pekala, R.W.; Mayer, S.T.; Kaschmitter, J.L.; Kong, F.M.

1993-07-01T23:59:59.000Z

374

Method of making molten carbonate fuel cell ceramic matrix tape  

DOE Patents [OSTI]

A method of making a thin, flexible, pliable matrix material for a molten carbonate fuel cell is described. The method comprises admixing particles inert in the molten carbonate environment with an organic polymer binder and ceramic particle. The composition is applied to a mold surface and dried, and the formed compliant matrix material removed.

Maricle, Donald L. (226 Forest La., Glastonbury, CT 06033); Putnam, Gary C. (47 Walker St., Manchester, CT 06040); Stewart, Jr., Robert C. (1230 Copper Hill Rd., West Suffield, CT 06093)

1984-10-23T23:59:59.000Z

375

The Woodland Carbon Code  

E-Print Network [OSTI]

The Woodland Carbon Code While society must continue to make every effort to reduce greenhouse gas a role by removing carbon dioxide from the atmosphere. The potential of woodlands to soak up carbon to help compensate for their carbon emissions. But before investing in such projects, people want to know

376

Preparation of polypyrrole-incorporated mesoporous carbon-based composites for confinement of Eu(III) within mesopores  

E-Print Network [OSTI]

e Mesoporous polymer-carbon composite (CMPEI/CMK-3) materials were successfully preparedPreparation of polypyrrole-incorporated mesoporous carbon-based composites for confinement of Eu processes. 1. Introduction A number of organic-inorganic or organic-organic composite materials have been

Boo, Jin-Hyo

377

Inorganic Carbon Turnover caused by Digestion of Carbonate Sands and Metabolic Activity of Holothurians  

SciTech Connect (OSTI)

Recent measurements have shown that holothurians (sea cucumbers) play an important role in the cycling of CaCO3 in tropical coral reef systems through ingestion and processing of carbonate sediment. In this study inorganic additional aspects of carbon turnover were determined in laboratory incubations of Holothuria atra, H. leucospilota and Stichopus herrmanni from One Tree Reef, Great Barrier Reef. The pH values of the gut lumen ranged from 6.1 to 6.7 in animals with empty digestive tracts as opposed to 7.0 to 7.6 when digestive tracts were filled with sediment. Empty gut volume estimates for H. atra and S. herrmanni were 36 ± 4 mL and 151 ± 14 mL, respectively. Based on these measurements it is estimated that these species process 19 ± 2kg and 80 ± 7kg CaCO3 sand yr-1 per individual, respectively. The annual dissolution rates of H. atra and S. herrmanni of 6.5±1.9g and 9.6±1.4g, respectively, suggest that 0.05±0.02% and 0.1±0.02% of the CaCO3 processed through their gut annually is dissolved. During the incubations the CaCO3 dissolution was 0.07±0.01%, 0.04±0.01% and 0.21±0.05% of the fecal casts for H. atra, H. leucospilota and S. herrmanni, respectively. The CaCO3 saturation state for both aragonite and calcite minerals during laboratory incubations decreased markedly due to a greater increase in dissolved inorganic carbon (DIC) relative to total alkalinity (AT) as a result of respiration by the animals. Our results support the hypothesis that deposit feeders such as sea cucumbers play an important ecological role in the coral reef CaCO3 cycle.

Schneider, Kenneth; Silverman, Jacob; Kravitz, Benjamin S.; Rivlin, Tanya; Schneider-Mor, Aya; Barbosa, Sergio; Byrne, Maria; Caldeira, Ken

2013-11-20T23:59:59.000Z

378

Mesoporous carbon materials  

DOE Patents [OSTI]

A conductive mesoporous carbon composite comprising conductive carbon nanoparticles contained within a mesoporous carbon matrix, wherein the conductive mesoporous carbon composite possesses at least a portion of mesopores having a pore size of at least 10 nm and up to 50 nm, and wherein the mesopores are either within the mesoporous carbon matrix, or are spacings delineated by surfaces of said conductive carbon nanoparticles when said conductive carbon nanoparticles are fused with each other, or both. Methods for producing the above-described composite, devices incorporating them (e.g., lithium batteries), and methods of using them, are also described.

Dai, Sheng; Fulvio, Pasquale Fernando; Mayes, Richard T.; Wang, Xiqing; Sun, Xiao-Guang; Guo, Bingkun

2014-09-09T23:59:59.000Z

379

http://webhelp.esri.com/arcgisdesktop/9.3/index.cfm?id=1840&pid=1837&topicname=Dissolve_(Data_Management) Dissolve Aggregates features based on specified attributes. It removes internal boundaries.  

E-Print Network [OSTI]

http://webhelp.esri.com/arcgisdesktop/9.3/index.cfm?id=1840&pid=1837&topicname://webhelp.esri.com/arcgisdesktop/9.3/index.cfm?id=1840&pid=1837&topicname=Dissolve_(Data_Management) Parameters: Input Features

Brownstone, Rob

380

Acid sorption regeneration process using carbon dioxide  

DOE Patents [OSTI]

Carboxylic acids are sorbed from aqueous feedstocks onto a solid adsorbent in the presence of carbon dioxide under pressure. The acids are freed from the sorbent phase by a suitable regeneration method, one of which is treating them with an organic alkylamine solution thus forming an alkylamine-carboxylic acid complex which thermally decomposes to the desired carboxylic acid and the alkylamine.

King, C. Judson (Kensington, CA); Husson, Scott M. (Anderson, SC)

2001-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


381

A CATALOG OF GALACTIC INFRARED CARBON STARS  

SciTech Connect (OSTI)

We collected almost all of the Galactic infrared carbon stars (IRCSs) from literature published up to the present to organize a catalog of 974 Galactic IRCSs in this paper. Some of their photometric properties in the near-, mid-, and far-infrared are discussed.

Chen, P. S. [National Astronomical Observatories/Yunnan Observatory and Key Laboratory for the Structure and Evolution of Celestial Objects, Chinese Academy of Sciences, Kunming 650011 (China); Yang, X. H., E-mail: iraspsc@yahoo.com.cn, E-mail: yangxh@cqu.edu.cn [Department of Physics, Chongqing University, Chongqing 400044 (China)

2012-02-15T23:59:59.000Z

382

Electrochemical formation of hydroxide for enhancing carbon dioxide and acid gas uptake by a solution  

DOE Patents [OSTI]

A system is described for forming metal hydroxide from a metal carbonate utilizing a water electrolysis cell having an acid-producing anode and a hydroxyl-producing cathode immersed in a water solution of sufficient ionic content to allow an electric current to pass between the hydroxyl-producing cathode and the acid-producing anode. A metal carbonate, in particular water-insoluble calcium carbonate or magnesium carbonate, is placed in close proximity to the acid-producing anode. A direct current electrical voltage is provided across the acid-producing anode and the hydroxyl-producing cathode sufficient to generate acid at the acid-producing anode and hydroxyl ions at the hydroxyl-producing cathode. The acid dissolves at least part of the metal carbonate into metal and carbonate ions allowing the metal ions to travel toward the hydroxyl-producing cathode and to combine with the hydroxyl ions to form the metal hydroxide. The carbonate ions travel toward the acid-producing anode and form carbonic acid and/or water and carbon dioxide. Among other uses, the metal hydroxide formed can be employed to absorb acid gases such as carbon dioxide from a gas mixture. The invention can also generate hydrogen and oxidative gases such as oxygen or chlorine.

Rau, Gregory Hudson (Castro Valley, CA)

2012-05-15T23:59:59.000Z

383

E-Print Network 3.0 - area uv transparent Sample Search Results  

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

90 A. Biographical Information: Donald P. Morris Summary: . The role of photochemical degradation of dissolved organic carbon in regulating the UV transparency... , climate,...

384

acute behavioral effects: Topics by E-print Network  

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

natural waters CO2 and dissolved organic carbon (DOC). Acute toxicity was determined for C. dubia and P. promelas Grosell, Martin 251 Taking trophic cascades up a level:...

385

Ultrafast Nonlinear Spectroscopy of Semiconducting Carbon Nanotubes  

E-Print Network [OSTI]

metallic nanotubes . . . . . . . . . . . . . . . . . Carbon2 Carbon Nanotubes Physical and ElectronicStructure of Carbon Nanotubes . . . . . . . . . .

Graham, Matthew Werden

2010-01-01T23:59:59.000Z

386

Ultrafast Nonlinear Spectroscopy of Semiconducting Carbon Nanotubes  

E-Print Network [OSTI]

2 Carbon Nanotubes Physical andElectronic Structure of Carbon Nanotubes . . . . . . . . . .Photophysics in Semiconducting Carbon Nanotubes . . . . .

Graham, Matthew Werden

2010-01-01T23:59:59.000Z

387

Nanocomposite fibers and film containing polyolefin and surface-modified carbon nanotubes  

DOE Patents [OSTI]

Methods for modifying carbon nanotubes with organic compounds are disclosed. The modified carbon nanotubes have enhanced compatibility with polyolefins. Nanocomposites of the organo-modified carbon nanotubes and polyolefins can be used to produce both fibers and films having enhanced mechanical and electrical properties, especially the elongation-to-break ratio and the toughness of the fibers and/or films.

Chu,Benjamin (Setauket, NY); Hsiao, Benjamin S. (Setauket, NY)

2010-01-26T23:59:59.000Z

388

Comprehensive study of carbon dioxide adsorption in the metalorganic frameworks M2(dobdc)  

E-Print Network [OSTI]

are historically slow, the need for mitigation of current CO2 emissions using carbon capture and sequestration (CCSComprehensive study of carbon dioxide adsorption in the metal­organic frameworks M2(dobdc) (M ¼ Mg of adsorption in the M2(dobdc)­CO2 adducts. Introduction Currently, 80% of global energy is supplied by carbon

389

19.1 Introduction Carbon sequestration programs on land and in the  

E-Print Network [OSTI]

Chapter 19 19.1 Introduction Carbon sequestration programs on land and in the oceans are gaining sequestration programs emphasize storing carbon in soil organic matter in agri- cultural fields,in woody sequestration and management include the feasibil- ity and permanence of the carbon sequestered, the scale

Jackson, Robert B.

390

Global Change Biology (2000) 6, 317328 Soil Carbon Sequestration and Land-Use Change: Processes and  

E-Print Network [OSTI]

Global Change Biology (2000) 6, 317­328 Soil Carbon Sequestration and Land-Use Change: Processes in enhanced soil carbon sequestration with changes in land-use and soil management. We review literature, and indicates the relative importance of some factors that influence the rates of organic carbon sequestration

Post, Wilfred M.

391

The Role of Dissolved Oxygen in Hard Clam Aquaculture1 Kerry Weber, Elise Hoover, Leslie Sturmer, and Shirley Baker2  

E-Print Network [OSTI]

FA152 The Role of Dissolved Oxygen in Hard Clam Aquaculture1 Kerry Weber, Elise Hoover, Leslie. Visit the EDIS Web Site at http://edis.ifas.ufl.edu. 2. Kerry Weber, former graduate student; Elise

Florida, University of

392

A measurement of the absorption of liquid argon scintillation light by dissolved nitrogen at the part-per-million level  

E-Print Network [OSTI]

We report on a measurement of the absorption length of scintillation light in liquid argon due to dissolved nitrogen at the part-per-million (ppm) level. We inject controlled quantities of nitrogen into a high purity volume ...

Jones, Benjamin James Poyner

393

Plant responses to phosphorus-deficiency stress: the role of organic acids in P mobilization from iron oxide and P acquisition by sorghum  

E-Print Network [OSTI]

-deficiency stress are organic-acid exudation from the roots and increased phosphatase activity. Organic-acid-induced P release from iron-oxide surfaces was studied using synthetic iron oxides. The amounts of P released and Fe dissolved from ferrihydrite and goethite...

Johnson, Sarah Elizabeth

1999-01-01T23:59:59.000Z

394

Doping of carbon foams for use in energy storage devices  

DOE Patents [OSTI]

A polymeric foam precursor, wetted with phosphoric acid, is pyrolyzed in an inert atmosphere to produce an open-cell doped carbon foam, which is utilized as a lithium intercalation anode in a secondary, organic electrolyte battery. Tests were conducted in a cell containing an organic electrolyte and using lithium metal counter and reference electrodes, with the anode located there between. Results after charge and discharge cycling, for a total of 6 cycles, indicated a substantial increase in the energy storage capability of the phosphorus doped carbon foam relative to the undoped carbon foam, when used as a rechargeable lithium ion battery. 3 figs.

Mayer, S.T.; Pekala, R.W.; Morrison, R.L.; Kaschmitter, J.L.

1994-10-25T23:59:59.000Z

395

Doping of carbon foams for use in energy storage devices  

DOE Patents [OSTI]

A polymeric foam precursor, wetted with phosphoric acid, is pyrolyzed in an inert atmosphere to produce an open-cell doped carbon foam, which is utilized as a lithium intercalation anode in a secondary, organic electrolyte battery. Tests were conducted in a cell containing an organic electrolyte and using lithium metal counter and reference electrodes, with the anode located therebetween. Results after charge and discharge cycling, for a total of 6 cycles, indicated a substantial increase in the energy storage capability of the phosphorus doped carbon foam relative to the undoped carbon foam, when used as a rechargeable lithium ion battery.

Mayer, Steven T. (San Leandro, CA); Pekala, Richard W. (Pleasant Hill, CA); Morrison, Robert L. (Modesto, CA); Kaschmitter, James L. (Pleasanton, CA)

1994-01-01T23:59:59.000Z

396

Chapter 10: Impacts of natural disturbance on soil carbon dynamics in forest ecosystems.  

E-Print Network [OSTI]

Chapter 10: Impacts of natural disturbance on soil carbon dynamics in forest ecosystems. Steven T University, Flagstaff, AZ INTRODUCTION Forest soils are entities within themselves, self- organized and highly resilient over time. The transfer of energy bound in carbon (C) molecules drives the organization

397

Tailoring the properties of organic aerogels  

SciTech Connect (OSTI)

We have recently succeeded in producing a new class of organic (or carbon) aerogels whose electrical, mechanical, and other properties are superior to those of the metal alkoxides. By tailoring properties to specific applications, we hope to achieve aerogels with even better performance. We have already tested carbon aerogels for use in inertial-confinement fusion targets and are currently studying applications to other technologies, such as battery electrodes, catalyst supports, and gas filters. In several of these applications, the permeability of the carbon aerogels-that is, their resistance to fluid flow-is crucial to their performance. Here, we describe briefly the synthesis of organic aerogels and present the results of our permeability studies.

Not Available

1993-05-01T23:59:59.000Z

398

Ernesto Joselevich Research Summary -May 2008 Molecular Wires: From Self-Organization to Functional Nanosystems  

E-Print Network [OSTI]

-dimensional nanostructures, such as carbon nanotubes, inorganic nanowires and polymers, their integration into functional the development of epitaxial approaches to carbon nanotube organization, namely, the directed growth of carbon highly straight, kinked, wavy, crossed8 , serpentine9 and looped. A second contribution has been

Martin, Jan M.L.

399

Effect of low po? on growth of bacteria and on loss of soluble carbon from maize roots under hydroponic conditions  

E-Print Network [OSTI]

. . . . . . . . . . . . . . . . . . . . . . - ~ -. 16 Analysis of soluble sugars and total organic carbon (TOC) in root extracts and in the nutrient solution. . . . . . . . . . . . . . . . . 17 vii Page RESULTS. 19 Effect of p02 on soluble total organic carbon (TOC) in roots and solution (2 kpa... on root and shoot dry matter (2 kPa vs. 20. 9 kPa 02). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . ~ . ~ . . . . . . . . . 49 Effect of p02 on soluble total organic carbon (TOC) in roots snd solution (0 kPa vs. 20. 9 kPa 02...

Coker, Dennis Lee

1992-01-01T23:59:59.000Z

400

Method and reaction pathway for selectively oxidizing organic compounds  

DOE Patents [OSTI]

A method of selectively oxidizing an organic compound in a single vessel comprises: a) combining an organic compound, an acid solution in which the organic compound is soluble, a compound containing two oxygen atoms bonded to one another, and a metal ion reducing agent capable of reducing one of such oxygen atoms, and thereby forming a mixture; b) reducing the compound containing the two oxygen atoms by reducing one of such oxygen atoms with the metal ion reducing agent to, 1) oxidize the metal ion reducing agent to a higher valence state, and 2) produce an oxygen containing intermediate capable of oxidizing the organic compound; c) reacting the oxygen containing intermediate with the organic compound to oxidize the organic compound into an oxidized organic intermediate, the oxidized organic intermediate having an oxidized carbon atom; d) reacting the oxidized organic intermediate with the acid counter ion and higher valence state metal ion to bond the acid counter ion to the oxidized carbon atom and thereby produce a quantity of an ester incorporating the organic intermediate and acid counter ion; and e) reacting the oxidized organic intermediate with the higher valence state metal ion and water to produce a quantity of alcohol which is less than the quantity of ester, the acid counter ion incorporated in the ester rendering the carbon atom bonded to the counter ion less reactive with the oxygen containing intermediate in the mixture than is the alcohol with the oxygen containing intermediate.

Camaioni, Donald M. (Richland, WA); Lilga, Michael A. (Richland, WA)

1998-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


401

Carbon fuel cells with carbon corrosion suppression  

DOE Patents [OSTI]

An electrochemical cell apparatus that can operate as either a fuel cell or a battery includes a cathode compartment, an anode compartment operatively connected to the cathode compartment, and a carbon fuel cell section connected to the anode compartment and the cathode compartment. An effusion plate is operatively positioned adjacent the anode compartment or the cathode compartment. The effusion plate allows passage of carbon dioxide. Carbon dioxide exhaust channels are operatively positioned in the electrochemical cell to direct the carbon dioxide from the electrochemical cell.

Cooper, John F. (Oakland, CA)

2012-04-10T23:59:59.000Z

402

Soil metagenomics and carbon cycling  

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

Soil metagenomics and carbon cycling Soil metagenomics and carbon cycling Establishing a foundational understanding of the microbial and ecosystem factors that control carbon...

403

Carbon Nanostructure-Based Sensors  

E-Print Network [OSTI]

Control of Single-Walled Carbon Nanotube Functionalization.M. S. Characterizing carbon nanotube samples with resonancewith a Single-Walled Carbon Nanotube Capacitor. Science

Sarkar, Tapan

2012-01-01T23:59:59.000Z

404

The Australian terrestrial carbon budget  

E-Print Network [OSTI]

Australian terrestrial carbon budget Open Access 3 , G. P.The Australian terrestrial carbon budget Luo, C. , Mahowald,terrestrial carbon budget Richards, G. P. , Borough, C. ,

2013-01-01T23:59:59.000Z

405

Actinide partitioning from actual ICPP dissolved zirconium calcine using the TRUEX solvent  

SciTech Connect (OSTI)

The TRansUranic EXtraction process (TRUEX), as developed by E.P. Horwitz and coworkers at Argonne National Laboratory (ANL), is being evaluated as a TRU extraction process for Idaho Chemical Processing Plant (ICPP) wastes. A criteria that must be met during this evaluation, is that the aqueous raffinate must be below the 10 nCi/g limit specified in 10 CFR 61.55. A test was performed where the TRUEX solvent (0.2 M octyl(phenyl)-N-N-diisobutyl-carbamoylmethyl-phosphine oxide (CMPO), and 1.4 M tributylphosphate (TBP) in an Isopar-L diluent) was contacted with actual ICPP dissolved zirconium calcine. Two experimental flowsheets were used to determine TRU decontamination factors, and TRU, Zr, Fe, Cr, and Tc extraction, scrub, and strip distribution coefficients. Results from these two flowsheets show that >99.99% of the TRU alpha activity was removed from the acidic feed after three contacts with the TRUEX solvent (fresh solvent being used for each contact). The resulting aqueous raffinate solution contained an approximate TRU alpha activity of 0.02 nCi/g, which is well below the non-TRU waste limit of 10 nCi/g specified in 10 CFR 61.55. Favorable scrub and strip distribution coefficients were also observed for Am-241, Pu-238, and Pu-239, indicating the feasibility of recovering these isotopes from the TRUTEX solvent. A solution of 0.04 M 1-hydroxyethane-1,1-diphosphonic acid (HEDPA) in 0.04 M HNO{sub 3} was used to successfully strip the TRUs from the TRUEX solvent. The results of the test using actual ICPP dissolved zirconium calcine, and subsequent GTM evaluation, show the feasibility of removing TRUs from the dissolved zirconium calcine with the TRUEX solvent and the deleterious effects zirconium poses with the ICPP zirconium calcine waste. Test results using actual ICPP zirconium calcine reveal the necessity of preventing zirconium from following the TRUs.

Brewer, K.N.; Herbst, R.S.; Tranter, T.J. [and others

1995-05-01T23:59:59.000Z

406

Determination of Total Petroleum Hydrocarbons (TPH) Using Total Carbon Analysis  

SciTech Connect (OSTI)

Several methods have been proposed to replace the Freon(TM)-extraction method to determine total petroleum hydrocarbon (TPH) content. For reasons of cost, sensitivity, precision, or simplicity, none of the replacement methods are feasible for analysis of radioactive samples at our facility. We have developed a method to measure total petroleum hydrocarbon content in aqueous sample matrixes using total organic carbon (total carbon) determination. The total carbon content (TC1) of the sample is measured using a total organic carbon analyzer. The sample is then contacted with a small volume of non-pokar solvent to extract the total petroleum hydrocarbons. The total carbon content of the resultant aqueous phase of the extracted sample (TC2) is measured. Total petroleum hydrocarbon content is calculated (TPH = TC1-TC2). The resultant data are consistent with results obtained using Freon(TM) extraction followed by infrared absorbance.

Ekechukwu, A.A.

2002-05-10T23:59:59.000Z

407

Organization Chart - Home  

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

LSD Logo About Us People & Organization Research News & Events Safety Internal Resources Organization Chart Departments Scientific Staff Directory Committees Organization Chart...

408

Desalination with carbon aerogel electrodes. Revision 1  

SciTech Connect (OSTI)

Electrically regenerated electrosorption process (carbon aerogel CDI) was developed by LLNL for continuously removing ionic impurities from aqueous streams. A salt solution flows in a channel formed by numerous pairs of parallel carbon aerogel electrodes. Each electrode has a very high BET surface area (2-5.4x10{sup 6}ft{sup 2}lb{sup -1} or 400-1100 m{sup 2}g{sup -1}) and very low electrical resistivity ({le}40 m{Omega}). Ions are removed from the electrolyte by the electric field and electrosorbed onto the carbon aerogel. It is concluded that carbon aerogel CDI may be an energy-efficient alternative to electrodialysis and reverse osmosis for desalination of brackish water ({le}5000 ppM). The intrinsic energy required by this process is about QV/2, where Q is the stored electrical charge and V is the voltage between the electrodes, plus losses. Estimated requirement for desalination of a 2000 ppM feed is -0.53-2.5 Wh/gal{sup -1} (0.5-2.4 kJ L{sup -1}), depending on voltage, flow rate, cell dimensions, aerogel density, recovery ratio, etc. This assumes that 50-70% of the stored electrical energy is reclaimed during regeneration (electrical discharge). Though the energy requirement for desalination of sea water is also low, this application will be much more difficult. Additional work will be required for desalination of streams that contain more than 5000 ppM total dissolved solids (2000 ppM will require electrochemical cells with extremely tight, demanding tolerances). At this present time, the process is best suited for streams with dilute impurities, as recently demonstrated during a field test at LLNL Treatment Facility C.

Farmer, J.C.; Richardson, J.H.; Fix, D.V. [Lawrence Livermore National Lab., CA (United States); Thomson, S.L.; May, S.C. [Bechtel National, Inc., San Francisco, CA (United States)

1996-12-04T23:59:59.000Z

409

Modeling the downstream improvements in dissolved oxygen from aeration of Cherokee and Douglas releases  

SciTech Connect (OSTI)

This report is an evaluation of downstream improvements in dissolved oxygen (DO) which can be anticipated as a result of different levels of aeration at Cherokee and Douglas Dams. The report describes (a) field studies undertaken to describe late summer conditions for model calibration and verification; (b) development and calibration of unsteady flow and water quality models for the tailwater reaches from Cherokee and Douglas Dams to the Holston and French Broad River confluence at the head of Fort Loudoun Reservoir; and (c) model predictions of DO in the tailwater reaches and at their confluence (after mixing) with and without aeration. 7 refs., 47 figs., 4 tabs.

Hauser, G.E.; Beard, L.M.; Brown, R.T.; McKinnon, M.K.

1983-09-01T23:59:59.000Z

410

In Situ Bioreduction of Uranium (VI) to Submicromolar Levels and Reoxidation by Dissolved Oxygen  

SciTech Connect (OSTI)

Groundwater within Area 3 of the U.S. Department of Energy (DOE) Environmental Remediation Sciences Program (ERSP) Field Research Center at Oak Ridge, TN (ORFRC) contains up to 135 {micro}M uranium as U(VI). Through a series of experiments at a pilot scale test facility, we explored the lower limits of groundwater U(VI) that can be achieved by in-situ biostimulation and the effects of dissolved oxygen on immobilized uranium. Weekly 2 day additions of ethanol over a 2-year period stimulated growth of denitrifying, Fe(III)-reducing, and sulfate-reducing bacteria, and immobilization of uranium as U(IV), with dissolved uranium concentrations decreasing to low levels. Following sulfite addition to remove dissolved oxygen, aqueous U(VI) concentrations fell below the U.S. Environmental Protection Agency maximum contaminant limit (MCL) for drinking water (<30 {micro}g L{sup -1} or 0.126 {micro}M). Under anaerobic conditions, these low concentrations were stable, even in the absence of added ethanol. However, when sulfite additions stopped, and dissolved oxygen (4.0-5.5 mg L{sup -1}) entered the injection well, spatially variable changes in aqueous U(VI) occurred over a 60 day period, with concentrations increasing rapidly from <0.13 to 2.0 {micro}M at a multilevel sampling (MLS) well located close to the injection well, but changing little at an MLS well located further away. Resumption of ethanol addition restored reduction of Fe(III), sulfate, and U(VI) within 36 h. After 2 years of ethanol addition, X-ray absorption near-edge structure spectroscopy (XANES) analyses indicated that U(IV) comprised 60-80% of the total uranium in sediment samples. At the completion of the project (day 1260), U concentrations in MLS wells were less than 0.1 {micro}M. The microbial community at MLS wells with low U(VI) contained bacteria that are known to reduce uranium, including Desulfovibrio spp. and Geobacter spp., in both sediment and groundwater. The dominant Fe(III)-reducing species were Geothrix spp.

Wu, Weimin [ORNL; Carley, Jack M [ORNL; Luo, Jian [Stanford University; Ginder-Vogel, Matthew A. [Stanford University; Cardenas, Erick [Michigan State University, East Lansing; Leigh, Mary Beth [Michigan State University, East Lansing; Hwang, Chaichi [Miami University, Oxford, OH; Kelly, Shelly D [Argonne National Laboratory (ANL); Ruan, Chuanmin [ORNL; Wu, Liyou [University of Oklahoma, Norman; Van Nostrand, Joy [University of Oklahoma, Norman; Gentry, Terry J [ORNL; Lowe, Kenneth Alan [ORNL; Mehlhorn, Tonia L [ORNL; Carroll, Sue L [ORNL; Luo, Wensui [ORNL; Fields, Matthew Wayne [Miami University, Oxford, OH; Gu, Baohua [ORNL; Watson, David B [ORNL; Kemner, Kenneth M [Argonne National Laboratory (ANL); Marsh, Terence [Michigan State University, East Lansing; Tiedje, James [Michigan State University, East Lansing; Zhou, Jizhong [University of Oklahoma, Norman; Fendorf, Scott [Stanford University; Kitanidis, Peter K. [Stanford University; Jardine, Philip M [ORNL; Criddle, Craig [ORNL

2007-01-01T23:59:59.000Z

411

Inorganic-organic hybrid aerogels  

SciTech Connect (OSTI)

Organically modified silica aerogels were prepared by NH{sub 4}OH-catalyzed hydrolysis and condensation of RSi(OMe){sub 3} / Si(OMe){sub 4} mixtures, followed by supercritical drying of the alcogels with methanol or CO{sub 2}. Terminal alkyl or aryl groups, bridging groups or functional organic (methacryloxypropyl or glycidoxypropyl) groups were employed for R. By the proper choice of the organic groups, the RSi(OMe){sub 3} / Si(OMe){sub 4} ratio and the drying conditions, hydrophobic aerogels, being insensitive towards moisture, were obtained with no residual SiOH or Si-OMe groups left. The transparency and porosity of the organically modified aerogels was only slightly diminished relative to unmodified silica aerogels. The elastic constant of the aerogels was significantly influenced by the kind of organic groups. By pyrolysis of the phenyl-substituted aerogels, nanometer-sized carbon structures were generated. They partly coat the primary aerogel particles and provide a very high mass specific extinction in the wavelengths interval critical for thermal radiative transport.

Schubert, U.; Schwertfeger, F.; Huesing, N.; Seyfried, E. [Univ. Wuerzburg (Germany). Inst. fuer Anorganische Chemie

1994-12-31T23:59:59.000Z

412

Microwave-assisted synthesis of carbon nanotubes from tannin, lignin, and derivatives  

SciTech Connect (OSTI)

A method of synthesizing carbon nanotubes. In one embodiment, the method includes the steps of: (a) dissolving a first amount of a first transition-metal salt and a second amount of a second transition-metal salt in water to form a solution; (b) adding a third amount of tannin to the solution to form a mixture; (c) heating the mixture to a first temperature for a first duration of time to form a sample; and (d) subjecting the sample to a microwave radiation for a second duration of time effective to produce a plurality of carbon nanotubes.

Viswanathan, Tito

2014-06-17T23:59:59.000Z

413

Method of making carbon-carbon composites  

DOE Patents [OSTI]

A process for making a carbon-carbon composite having a combination of high crystallinity, high strength, high modulus and high thermal and electrical conductivity. High-modulus/high-strength mesophase derived carbon fibers are woven into a suitable cloth. Layers of this easily graphitizable woven cloth are covered with petroleum or coal tar pitch and pressed at a temperature a few degrees above the softening point of the pitch to form a green laminated composite. The green composite is restrained in a suitable fixture and heated slowly to carbonize the pitch binder. The carbonized composite is then impregnated several times with pitch by covering the composite with hot pitch under pressure. The composites are given a heat treatment between each impregnation step to crack up the infiltrated carbon and allow additional pitch to enter the microstructure during the next impregnation cycle. The impregnated composites are then given a final heat treatment in the range 2500.degree. to 3000.degree. C. to fully graphitize the fibers and the matrix carbon. The composites are then infiltrated with pyrolytic carbon by chemical vapor deposition in the range 1000.degree. to 1300.degree. C. at a reduced pressure for approximately one hundred and fifty (150) hours.

Engle, Glen B. (16716 Martincoit Rd., Poway, CA 92064)

1991-01-01T23:59:59.000Z

414

Mineral mesopore effects on nitrogenous organic matter Andrew R. Zimmermana,  

E-Print Network [OSTI]

as sequestration of pollutants in soils and sediments (Luthy et al., 1997), turnover of natural soil organic carbon that organic matter (OM) may be protected from enzymatic degradation by sequestration within mineral mesopores observations. These results provide a potential mechanism for the selective sequestration and preservation

Chorover, Jon

415

Melody Meyer: Organic Foods Distributor  

E-Print Network [OSTI]

are into green building, reducing carbon footprint, trackingour carbon footprint. There aren’t many companies that areuse, offsetting our carbon footprint. The Rockland facility

Farmer, Ellen

2010-01-01T23:59:59.000Z

416

Carbon nanotube nanoelectrode arrays  

DOE Patents [OSTI]

The present invention relates to microelectode arrays (MEAs), and more particularly to carbon nanotube nanoelectrode arrays (CNT-NEAs) for chemical and biological sensing, and methods of use. A nanoelectrode array includes a carbon nanotube material comprising an array of substantially linear carbon nanotubes each having a proximal end and a distal end, the proximal end of the carbon nanotubes are attached to a catalyst substrate material so as to form the array with a pre-determined site density, wherein the carbon nanotubes are aligned with respect to one another within the array; an electrically insulating layer on the surface of the carbon nanotube material, whereby the distal end of the carbon nanotubes extend beyond the electrically insulating layer; a second adhesive electrically insulating layer on the surface of the electrically insulating layer, whereby the distal end of the carbon nanotubes extend beyond the second adhesive electrically insulating layer; and a metal wire attached to the catalyst substrate material.

Ren, Zhifeng (Newton, MA); Lin, Yuehe (Richland, WA); Yantasee, Wassana (Richland, WA); Liu, Guodong (Fargo, ND); Lu, Fang (Burlingame, CA); Tu, Yi (Camarillo, CA)

2008-11-18T23:59:59.000Z

417

Carbon Monoxide Safety Tips  

E-Print Network [OSTI]

Protect yourself and your family from the deadly effects of carbon monoxide--a colorless, odorless poisonous gas. This publication describes the warning signs of carbon monoxide exposure and includes a home safety checklist....

Shaw, Bryan W.; Garcia, Monica L.

1999-07-26T23:59:59.000Z

418

A three-phase free boundary problem with melting ice and dissolving gas  

E-Print Network [OSTI]

We develop a mathematical model for a three-phase free boundary problem in one dimension that involves the interactions between gas, water and ice. The dynamics are driven by melting of the ice layer, while the pressurized gas also dissolves within the meltwater. The model incorporates a Stefan condition at the water-ice interface along with Henry's law for dissolution of gas at the gas-water interface. We employ a quasi-steady approximation for the phase temperatures and then derive a series solution for the interface positions. A non-standard feature of the model is an integral free boundary condition that arises from mass conservation owing to changes in gas density at the gas-water interface, which makes the problem non-self-adjoint. We derive a two-scale asymptotic series solution for the dissolved gas concentration, which because of the non-self-adjointness gives rise to a Fourier series expansion in eigenfunctions that do not satisfy the usual orthogonality conditions. Numerical simulations of the original governing equations are used to validate the series approximations.

Maurizio Ceseri; John M. Stockie

2014-11-05T23:59:59.000Z

419

ESM 271 Carbon Footprints and Carbon Accounting Instructor: Sangwon Suh  

E-Print Network [OSTI]

1 ESM 271 Carbon Footprints and Carbon Accounting Instructor: Sangwon Suh Bren hall 3422, suh Week 1: Introduction to carbon footprint and carbon account - Background: carbon awareness, major out a report or a web site about carbon footprint results of a product or of a company. Write a two

California at Santa Barbara, University of

420

Big Sky Carbon Atlas  

DOE Data Explorer [Office of Scientific and Technical Information (OSTI)]

(Acknowledgment to the Big Sky Carbon Sequestration Partnership (BSCSP); see home page at http://www.bigskyco2.org/)

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


421

Intro to Carbon Sequestration  

ScienceCinema (OSTI)

NETL's Carbon Sequestration Program is helping to develop technologies to capture, purify, and store carbon dioxide (CO2) in order to reduce greenhouse gas emissions without adversely influencing energy use or hindering economic growth. Carbon sequestration technologies capture and store CO2 that would otherwise reside in the atmosphere for long periods of time.

None

2010-01-08T23:59:59.000Z

422

Intro to Carbon Sequestration  

SciTech Connect (OSTI)

NETL's Carbon Sequestration Program is helping to develop technologies to capture, purify, and store carbon dioxide (CO2) in order to reduce greenhouse gas emissions without adversely influencing energy use or hindering economic growth. Carbon sequestration technologies capture and store CO2 that would otherwise reside in the atmosphere for long periods of time.

2008-03-06T23:59:59.000Z

423

SmallholderSmallholder CarbonCarbon AgroforestryAgroforestry && Carbon for Poverty ReductionCarbon for Poverty Reduction  

E-Print Network [OSTI]

SmallholderSmallholder CarbonCarbon AgroforestryAgroforestry && Carbon for Poverty ReductionCarbon for Poverty Reduction Roundtable (CAPR)Roundtable (CAPR) GEO Forest Monitoring SymposiumGEO Forest Monitoring)Amazon Initiative Consortium (IA) #12;Carbon for Poverty Reduction Roundtable (CAPR)Carbon for Poverty Reduction

424

Significance of Isotopically Labile Organic Hydrogen in Thermal Maturation of Organic Matter  

SciTech Connect (OSTI)

Isotopically labile organic hydrogen in fossil fuels occupies chemical positions that participate in isotopic exchange and in chemical reactions during thermal maturation from kerogen to bitumen, oil and gas. Carbon-bound organic hydrogen is isotopically far less exchangeable than hydrogen bound to nitrogen, oxygen, or sulfur. We explore why organic hydrogen isotope ratios express a relationship with organic nitrogen isotope ratios in kerogen at low to moderate maturity. We develop and apply new techniques to utilize organic D/H ratios in organic matter fractions and on a molecular level as tools for exploration for fossil fuels and for paleoenvironmental research. The scope of our samples includes naturally and artificially matured substrates, such as coal, shale, oil and gas.

Arndt Schimmelmann; Maria Mastalerz

2010-03-30T23:59:59.000Z

425

Organic fuel cells and fuel cell conducting sheets  

DOE Patents [OSTI]

A passive direct organic fuel cell includes an organic fuel solution and is operative to produce at least 15 mW/cm.sup.2 when operating at room temperature. In additional aspects of the invention, fuel cells can include a gas remover configured to promote circulation of an organic fuel solution when gas passes through the solution, a modified carbon cloth, one or more sealants, and a replaceable fuel cartridge.

Masel, Richard I. (Champaign, IL); Ha, Su (Champaign, IL); Adams, Brian (Savoy, IL)

2007-10-16T23:59:59.000Z

426

Formation of Carbon Dwarfs  

E-Print Network [OSTI]

We consider the formation of dwarf carbon stars via accretion from a carbon AGB companion in light of the new 107 object sample of Downes et al. (2004). This sample is now large enough to allow good mass determination via comparison of a composite spectrum to theoretical atmospheric models. Carbon dwarfs of spectral type M are indeed main sequence M dwarfs with enhanced metallicity and carbon abundance. We also calculate the predicted abundance of both M and of F/G carbon dwarfs, and show that the latter should be falsifiable in the near future.

Charles L. Steinhardt; Dimitar D. Sasselov

2012-01-27T23:59:59.000Z

427

Using dissolved noble gas and isotopic tracers to evaluate the vulnerability of groundwater resources in a small, high elevation catchment to predicted climate changes  

SciTech Connect (OSTI)

We use noble gas concentrations and multiple isotopic tracers in groundwater and stream water in a small high elevation catchment to provide a snapshot of temperature, altitude, and physical processes at the time of recharge; and to determine subsurface residence times of different groundwater components. They identify three sources that contribute to groundwater flow: (1) seasonal groundwater recharge with short travel times, (2) water from bedrock aquifers that have elevated radiogenic {sup 4}He, and (3) upwelling of deep fluids that have 'mantle' helium and hydrothermal carbon isotope signatures. Although a bimodal distribution in apparent groundwater age indicates that groundwater storage times range from less than a year to several decades, water that recharges seasonally is the largest likely contributor to stream baseflow. Under climate change scnearios with earlier snowmelt, the groundwater that moves through the alluvial aquifer seasonally will be depleted earlier, providing less baseflow and possible extreme low flows in the creek during summer and fall. Dissolved noble gas measurements indciate recharge temperatures are 5 to 11 degrees higher than would be expected for direct influx of snowmelt, and that excess air concentrations are lower than would be expected for recharge through bedrock fractures. Instead, recharge likely occurs over diffuse vegetated areas, as indicated by {delta}{sup 13}C-DIC values that are consistent with incorporation of CO{sub 2} from soil respiration. Recharge temperatures are close to or slightly higher than mean annual air temperature, and are consistent with recharge during May and June, when snowpack melting occurs.

Singleton, M J; Moran, J E

2009-10-02T23:59:59.000Z

428

Carbon in detonations  

SciTech Connect (OSTI)

We review three principal results from a five year study of carbon and its properties in detonations and discuss the implications of these results to the behavior of explosives. We first present a new determination of the carbon melt line from release wave velocity measurements in the shocked state. We then outline a colloidal theory of carbon clustering which from diffusion limited coagulation predicts a slow energy release rate for the carbon chemistry. Finally, we show the results from the examination of recovered soot. Here we see support for the colloid theory and find the diamond phase of carbon. The main theme of this paper is that the carbon in detonation products is in the form of a colloidal suspension of carbon clusters which grow through diffusion limited collisions. Even the final state is not bulk graphite or diamond, but is a collection of small, less than 100 /angstrom/A, diamond and graphitic clusters. 23 refs., 4 figs.

Johnson, J.D.

1989-01-01T23:59:59.000Z

429

Criticality experiments with low enriched UO/sub 2/ fuel rods in water containing dissolved gadolinium  

SciTech Connect (OSTI)

The results obtained in a criticality experiments program performed for British Nuclear Fuels, Ltd. (BNFL) under contract with the United States Department of Energy (USDOE) are presented in this report along with a complete description of the experiments. The experiments involved low enriched UO/sub 2/ and PuO/sub 2/-UO/sub 2/ fuel rods in water containing dissolved gadolinium, and are in direct support of BNFL plans to use soluble compounds of the neutron poison gadolinium as a primary criticality safeguard in the reprocessing of low enriched nuclear fuels. The experiments were designed primarily to provide data for validating a calculation method being developed for BNFL design and safety assessments, and to obtain data for the use of gadolinium as a neutron poison in nuclear chemical plant operations - particularly fuel dissolution. The experiments program covers a wide range of neutron moderation (near optimum to very under-moderated) and a wide range of gadolinium concentration (zero to about 2.5 g Gd/l). The measurements provide critical and subcritical k/sub eff/ data (1 greater than or equal to k/sub eff/ greater than or equal to 0.87) on fuel-water assemblies of UO/sub 2/ rods at two enrichments (2.35 wt % and 4.31 wt % /sup 235/U) and on mixed fuel-water assemblies of UO/sub 2/ and PuO/sub 2/-UO/sub 2/ rods containing 4.31 wt % /sup 235/U and 2 wt % PuO/sub 2/ in natural UO/sub 2/ respectively. Critical size of the lattices was determined with water containing no gadolinium and with water containing dissolved gadolinium nitrate. Pulsed neutron source measurements were performed to determine subcritical k/sub eff/ values as additional amounts of gadolinium were successively dissolved in the water of each critical assembly. Fission rate measurements in /sup 235/U using solid state track recorders were made in each of the three unpoisoned critical assemblies, and in the near-optimum moderated and the close-packed poisoned assemblies of this fuel.

Bierman, S.R.; Murphy, E.S.; Clayton, E.D.; Keay, R.T.

1984-02-01T23:59:59.000Z

430

GEOC R Lee Penn Sunday, March 25, 2012 12 -Biogeochemical transformation of Fe-and Mn-along a redox gradient: Implications for carbon sequestration  

E-Print Network [OSTI]

a redox gradient: Implications for carbon sequestration within the Christina River Basin Critical Zone States Organic carbon (C)-mineral complexation mechanism is crucial in C sequestration. It is a function

Sparks, Donald L.

431

Isoreticular metal-organic frameworks, process for forming the same, and systematic design of pore size and functionality therein, with application for gas storage  

DOE Patents [OSTI]

An isoreticular metal-organic framework (IRMOF) and method for systematically forming the same. The method comprises the steps of dissolving at least one source of metal cations and at least one organic linking compound in a solvent to form a solution; and crystallizing the solution under predetermined conditions to form a predetermined IRMOF. At least one of functionality, dimension, pore size and free volume of the IRMOF is substantially determined by the organic linking compound.

Yaghi, Omar M.; Eddaoudi, Mohamed; Li, Hailian; Kim, Jaheon; Rosi, Nathaniel

2005-08-16T23:59:59.000Z

432

Standard practices for dissolving glass containing radioactive and mixed waste for chemical and radiochemical analysis  

E-Print Network [OSTI]

1.1 These practices cover techniques suitable for dissolving glass samples that may contain nuclear wastes. These techniques used together or independently will produce solutions that can be analyzed by inductively coupled plasma atomic emission spectroscopy (ICP-AES), inductively coupled plasma mass spectrometry (ICP-MS), atomic absorption spectrometry (AAS), radiochemical methods and wet chemical techniques for major components, minor components and radionuclides. 1.2 One of the fusion practices and the microwave practice can be used in hot cells and shielded hoods after modification to meet local operational requirements. 1.3 The user of these practices must follow radiation protection guidelines in place for their specific laboratories. 1.4 Additional information relating to safety is included in the text. 1.5 The dissolution techniques described in these practices can be used for quality control of the feed materials and the product of plants vitrifying nuclear waste materials in glass. 1.6 These pr...

American Society for Testing and Materials. Philadelphia

2000-01-01T23:59:59.000Z

433

Using Renewable Energy Purchases to Achieve Institutional Carbon Goals: A Review of Current Practices and Considerations  

SciTech Connect (OSTI)

With organizations and individuals increasingly interested in accounting for their carbon emissions, greater attention is being placed on how to account for the benefits of various carbon mitigation actions available to consumers and businesses. Generally, organizations can address their own carbon emissions through energy efficiency, fuel switching, on-site renewable energy systems, renewable energy purchased from utilities or in the form of renewable energy certificates (RECs), and carbon offsets. This paper explores the role of green power and carbon offsets in carbon footprinting and the distinctions between the two products. It reviews how leading greenhouse gas (GHG) reporting programs treat green power purchases and discusses key issues regarding how to account for the carbon benefits of renewable energy. It also discusses potential double counting if renewable energy generation is used in multiple markets.

Bird, L.; Sumner, J.

2011-01-01T23:59:59.000Z

434

Dissolved Nutrient Retention Dynamics in River Networks: A Modeling Investigation of Transient Flow and Scale Effects  

SciTech Connect (OSTI)

In this paper, we use a dynamic network flow model, coupled with a transient storage zone biogeochemical model, to simulate dissolved nutrient removal processes at the channel network scale. We have explored several scenarios in respect of the combination of rainfall variability, and the biological and geomorphic characteristics of the catchment, to understand the dominant controls on removal and delivery of dissolved nutrients (e.g., nitrate). These model-based theoretical analyses suggested that while nutrient removal efficiency is lower during flood events compared to during baseflow periods, flood events contribute significantly to bulk nutrient removal, whereas bulk removal during baseflow periods is less. This is due to the fact that nutrient supply is larger during flood events; this trend is even stronger in large rivers. However, the efficiency of removal during both periods decreases in larger rivers, however, due to (i) increasing flow velocities and thus decreasing residence time, and (ii) increasing flow depth, and thus decreasing nutrient uptake rates. Besides nutrient removal processes can be divided into two parts: in the main channel and in the hyporheic transient storage zone. When assessing their relative contributions the size of the transient storage zone is a dominant control, followed by uptake rates in the main channel and in the transient storage zone. Increasing size of the transient storage zone with downstream distance affects the relative contributions to nutrient removal of the water column and the transient storage zone, which also impacts the way nutrient removal rates scale with increasing size of rivers. Intra-annual hydrologic variability has a significant impact on removal rates at all scales: the more variable the streamflow is, compared to mean discharge, the less nutrient is removed in the channel network. A scale-independent first order uptake coefficient, ke, estimated from model simulations, is highly dependent on the relative size of the transient storage zone and how it changes in the downstream direction, as well as the nature of hydrologic variability.

Ye, Sheng; Covino, Timothy P.; Sivapalan, Murugesu; Basu, Nandita; Li, Hongyi; Wang, Shaowen

2012-06-30T23:59:59.000Z

435

CARBON BED MERCURY EMISSIONS CONTROL FOR MIXED WASTE TREATMENT  

SciTech Connect (OSTI)

Mercury has had various uses in nuclear fuel reprocessing and other nuclear processes, and so is often present in radioactive and mixed (both radioactive and hazardous according tohe Resource Conservation and Recovery Act) wastes. Depending on regulatory requirements, the mercury in the off-gas must be controlled with sometimes very high efficiencies. Compliance to the Hazardous Waste Combustor (HWC) Maximum Achievable Control Technology (MACT) standards can require off-gas mercury removal efficiencies up to 99.999% for thermally treating some mixed waste streams. Several test programs have demonstrated this level of off-gas mercury control using fixed beds of granular sulfur-impregnated activated carbon. Other results of these tests include: (a) The depth of the mercury control mass transfer zone was less than 15-30 cm for the operating conditions of these tests, (b) MERSORB® carbon can sorb Hg up to 19 wt% of the carbon mass, and (c) the spent carbon retained almost all (98 – 99.99%) of the Hg; but when even a small fraction of the total Hg dissolves, the spent carbon can fail the TCLP test when the spent carbon contains high Hg concentrations. Localized areas in a carbon bed that become heated through heat of adsorption, to temperatures where oxidation occurs, are referred to as “bed hot spots.” Carbon bed hot spots must be avoided in processes that treat radioactive and mixed waste. Key to carbon bed hot spot mitigation are (a) designing for sufficient gas velocity, for avoiding gas flow maldistribution, and for sufficient but not excessive bed depth, (b) monitoring and control of inlet gas flowrate, temperature, and composition, (c) monitoring and control of in-bed and bed outlet gas temperatures, and (d) most important, monitoring of bed outlet CO concentrations. An increase of CO levels in the off-gas downstream of the carbon bed to levels about 50-100 ppm higher than the inlet CO concentration indicate CO formation in the bed, caused by carbon bed hot spots. Corrective actions must be implemented quickly if bed hot spots are detected, using a graded approach and sequence starting with corrective actions that are simple, quick, cause the least impact to the process, and are easiest to recover from. Multiple high and high-high alarm levels should be used, with appropriate corrective actions for each level.

Nick Soelberg; Joe Enneking

2010-11-01T23:59:59.000Z

436

Investigation of the organic matter in inactive nuclear tank liquids. Environmental Restoration Program  

SciTech Connect (OSTI)

Environmental Protection Agency (EPA) methodology for regulatory organics fails to account for the organic matter that is suggested by total organic carbon (TOC) analysis in the Oak Ridge National Laboratory (ORNL) inactive nuclear waste-tank liquids and sludges. Identification and measurement of the total organics are needed to select appropriate waste treatment technologies. An initial investigation was made of the nature of the organics in several waste-tank liquids. This report details the analysis of ORNL wastes.

Schenley, R.L.; Griest, W.H.

1990-08-01T23:59:59.000Z

437

ORGANIC CHEMISTRY UCLA Organic Chemistry Faculty  

E-Print Network [OSTI]

ORGANIC CHEMISTRY UCLA Organic Chemistry Faculty perform research in molecular machines, exotic CHEMISTRY FACULTY RESEARCH INTERESTS Anne M. Andrews, Professor-in-Residence: Understanding how areas of interest include cross- coupling reactions, green chemistry, heterocycle synthesis, and natural

Levine, Alex J.

438

Increasing subterranean mobilization of organic contaminants and petroleum by aqueous thermal oxidation  

DOE Patents [OSTI]

In situ hydrous pyrolysis/partial oxidation of organics at the site of the organics constrained in an subsurface reservoir produces surfactants that can form an oil/water emulsion that is effectively removed from an underground formation. The removal of the oil/water emulsions is particularly useful in several applications, e.g., soil contaminant remediation and enhanced oil recovery operations. A portion of the constrained organics react in heated reservoir water with injected steam containing dissolved oxygen gas at ambient reservoir conditions to produce such surfactants.

Leif, Roald N. (San Francisco, CA); Knauss, Kevin G. (Livermore, CA); Newmark, Robin L. (Livermore, CA); Aines, Roger D. (Livermore, CA); Eaker, Craig (Alta Loma, CA)

2002-01-01T23:59:59.000Z

439

SOUTHWEST REGIONAL PARTNERSHIP ON CARBON SEQUESTRATION  

SciTech Connect (OSTI)

The Southwest Partnership Region includes six whole states, including Arizona, Colorado, Kansas, New Mexico, Oklahoma, and Utah, roughly one-third of Texas, and significant portions of adjacent states. The Partnership comprises a large, diverse group of expert organizations and individuals specializing in carbon sequestration science and engineering, as well as public policy and outreach. The main objective of the Southwest Partnership project is to achieve an 18% reduction in carbon intensity by 2012. The Partnership made great progress in this first year. Action plans for possible Phase II carbon sequestration pilot tests in the region are almost finished, including both technical and non-technical aspects necessary for developing and carrying out these pilot tests. All partners in the Partnership are taking an active role in evaluating and ranking optimum sites and technologies for capture and storage of CO{sub 2} in the Southwest Region. We are identifying potential gaps in all aspects of potential sequestration deployment issues.

Brian McPherson; Rick Allis; Barry Biediger; Joel Brown; Jim Cappa; George Guthrie; Richard Hughes; Eugene Kim; Robert Lee; Dennis Leppin; Charles Mankin; Orman Paananen; Rajesh Pawar; Tarla Peterson; Steve Rauzi; Jerry Stuth; Genevieve Young

2004-11-01T23:59:59.000Z

440

Carbon dioxide sensor  

DOE Patents [OSTI]

The present invention generally relates to carbon dioxide (CO.sub.2) sensors. In one embodiment, the present invention relates to a carbon dioxide (CO.sub.2) sensor that incorporates lithium phosphate (Li.sub.3PO.sub.4) as an electrolyte and sensing electrode comprising a combination of lithium carbonate (Li.sub.2CO.sub.3) and barium carbonate (BaCO.sub.3). In another embodiment, the present invention relates to a carbon dioxide (CO.sub.2) sensor has a reduced sensitivity to humidity due to a sensing electrode with a layered structure of lithium carbonate and barium carbonate. In still another embodiment, the present invention relates to a method of producing carbon dioxide (CO.sub.2) sensors having lithium phosphate (Li.sub.3PO.sub.4) as an electrolyte and sensing electrode comprising a combination of lithium carbonate (Li.sub.2CO.sub.3) and barium carbonate (BaCO.sub.3).

Dutta, Prabir K. (Worthington, OH); Lee, Inhee (Columbus, OH); Akbar, Sheikh A. (Hilliard, OH)

2011-11-15T23:59:59.000Z

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


441

A method of determining the dissolved oxygen in the moisture of a porous medium and some oxygen diffusion studies  

E-Print Network [OSTI]

this dissolved oxygen The sample chamber apparatus gives ocnsplcte seal of the bottle from the atmosphere The ohsabor does not require a large ameunt Of nitrogen Sb remove all the oxygen from it, It is easily portable and light in weight The proposed method... METHOD QF DETRHRIUIHO THE DISSOLVED OXmEK IE THE MOISTURE OF A POROUS ERDD% @AD SMfE QXYOEB DKFFUSIOE STUDIES ' INTRO DUO fQRF, I Oxygen, bas been known to be important in plant growth fox maay years There has been a great deal of xesearoh...

Runkles, Jack Ralph

1952-01-01T23:59:59.000Z

442

Comparison of the Carbon System Parameters at the Global CO2 Survey Crossover Locations in the North and South Pacific Ocean, 1990-1996  

SciTech Connect (OSTI)

As a collaborative program to measure global ocean carbon inventories and provide estimates of the anthropogenic carbon dioxide (C02) uptake by the oceans. the National Oceanic and Atmospheric Administration and the U.S. Department of Energy have sponsored the collection of ocean carbon measurements as part of the World Ocean Circulation Experiment and Ocean-Atmosphere Carbon Exchange Study cruises. The cruises discussed here occurred in the North and South Pacific from 1990 through 1996. The carbon parameters from these 30 crossover locations have been compared to ensure that a consistent global data set emerges from the survey cruises. !'he results indicate that for dissolved inorganic carbon. fugacity of C02• and pH. the a~:,rreements at most crossover locations are well within the design specifications for the global CO) survey: whereas. in the case of total alkaliniry. the agreement between crossover locations is not as close.

Feely, Richard A [NOAA, Pacific Marine Environmental Laboratory (PMEL); Lamb, Marilyn F. [NOAA, Pacific Marine Environmental Laboratory (PMEL); Greeley, Dana J. [NOAA, Pacific Marine Environmental Laboratory (PMEL); Wanninkhof, Rik [NOAA, Atlantic Oceanographic and Meteorological Laboratory (AOML)

1999-10-01T23:59:59.000Z

443

Self-Assembled Micro-Honeycomb Network of Single-Walled Carbon Nanotubes for Heterojunction Solar Cell  

E-Print Network [OSTI]

Self-Assembled Micro-Honeycomb Network of Single-Walled Carbon Nanotubes for Heterojunction Solar. Here, we propose a self-organized micro- honeycomb network structure of SWNTs obtained by water@photon.t.u-tokyo.ac.jp) Various forms of nano-carbon films such as random network of single-walled carbon nanotubes (SWNTs

Maruyama, Shigeo

444

Effect of chloride content of molten nitrate salt on corrosion of A516 carbon steel.  

SciTech Connect (OSTI)

The corrosion behavior of A516 carbon steel was evaluated to determine the effect of the dissolved chloride content in molten binary Solar Salt. Corrosion tests were conducted in a molten salt consisting of a 60-40 weight ratio of NaNO{sub 3} and KNO{sub 3} at 400{sup o}C and 450{sup o}C for up to 800 hours. Chloride concentrations of 0, 0.5 and 1.0 wt.% were investigated to determine the effect on corrosion of this impurity, which can be present in comparable amounts in commercial grades of the constituent salts. Corrosion rates were determined by descaled weight losses, corrosion morphology was examined by metallographic sectioning, and the types of corrosion products were determined by x-ray diffraction. Corrosion proceeded by uniform surface scaling and no pitting or intergranular corrosion was observed. Corrosion rates increased significantly as the concentration of dissolved chloride in the molten salt increased. The adherence of surface scales, and thus their protective properties, was degraded by dissolved chloride, fostering more rapid corrosion. Magnetite was the only corrosion product formed on the carbon steel specimens, regardless of chloride content or temperature.

Bradshaw, Robert W.; Clift, W. Miles

2010-11-01T23:59:59.000Z

445

Voluntary Carbon Confusion: A Consumer's Guide to Purchasing Carbon Offsets  

E-Print Network [OSTI]

Voluntary Carbon Confusion: A Consumer's Guide to Purchasing Carbon Offsets and Renewable Energy 4 Report Introduction 5 Product Types 5 A. Carbon Offsets 5 B. Certified Emission Reductions (CERs. Voluntary Carbon Confusion: A Consumer's Guide to Purchasing Carbon Offsets and Renewable Energy

Hoffman, Andrew J.

446

Carbon RRLs Carbon RRLs towards Ultra-compact HII Regions  

E-Print Network [OSTI]

Carbon RRLs Carbon RRLs towards Ultra-compact HII Regions Dana S. Balser D. Anish Roshi (Raman (Agnes Scott College) #12;Carbon RRLs Carbon Radio Recombination Lines (RRLs) NGC 2024 (Orion B) IC 1795 (W3) Palmer et al. (1967) #12;Carbon RRLs Photodissociation Regions (PDRs) Hollenbach & Tielens (1997

Balser, Dana S.

447

Would Border Carbon Adjustments prevent carbon leakage and heavy industry  

E-Print Network [OSTI]

No 52-2013 Would Border Carbon Adjustments prevent carbon leakage and heavy industry halshs-00870689,version1-7Oct2013 #12;Would Border Carbon Adjustments prevent carbon leakage and heavy The efficiency of unilateral climate policies may be hampered by carbon leakage and competitiveness losses

Paris-Sud XI, Université de

448

Cumulative Carbon and Just Allocation of the Global Carbon Commons  

E-Print Network [OSTI]

Cumulative Carbon and Just Allocation of the Global Carbon Commons R.T. Pierrehumbert1 on climate can be characterized by a single statistic, called Cumulative Carbon. This is the aggregate amount of carbon emitted in the form of carbon dioxide by activities such as fossil fuel burning and deforestation

Pierrehumbert, Raymond

449

Carbon Sequestration via Mineral Carbonation: Overview and Assessment  

E-Print Network [OSTI]

1 Carbon Sequestration via Mineral Carbonation: Overview and Assessment 14 March 2002 Howard Herzog overview and assessment of carbon sequestration by mineral carbonation (referred to as "mineral sequestration R&D. The first is that carbonates have a lower energy state than CO2. Therefore, at least

450

Mesoporous carbon materials  

DOE Patents [OSTI]

The invention is directed to a method for fabricating a mesoporous carbon material, the method comprising subjecting a precursor composition to a curing step followed by a carbonization step, the precursor composition comprising: (i) a templating component comprised of a block copolymer, (ii) a phenolic compound or material, (iii) a crosslinkable aldehyde component, and (iv) at least 0.5 M concentration of a strong acid having a pKa of or less than -2, wherein said carbonization step comprises heating the precursor composition at a carbonizing temperature for sufficient time to convert the precursor composition to a mesoporous carbon material. The invention is also directed to a mesoporous carbon material having an improved thermal stability, preferably produced according to the above method.

Dai, Sheng; Wang, Xiqing

2013-08-20T23:59:59.000Z

451

Mesoporous carbon materials  

DOE Patents [OSTI]

The invention is directed to a method for fabricating a mesoporous carbon material, the method comprising subjecting a precursor composition to a curing step followed by a carbonization step, the precursor composition comprising: (i) a templating component comprised of a block copolymer, (ii) a phenolic compound or material, (iii) a crosslinkable aldehyde component, and (iv) at least 0.5 M concentration of a strong acid having a pKa of or less than -2, wherein said carbonization step comprises heating the precursor composition at a carbonizing temperature for sufficient time to convert the precursor composition to a mesoporous carbon material. The invention is also directed to a mesoporous carbon material having an improved thermal stability, preferably produced according to the above method.

Dai, Sheng (Knoxville, TN); Wang, Xiqing (Oak Ridge, TN)

2012-02-14T23:59:59.000Z

452

Metabolic evolution of Escherichia coli strains that produce organic acids  

DOE Patents [OSTI]

This invention relates to the metabolic evolution of a microbial organism previously optimized for producing an organic acid in commercially significant quantities under fermentative conditions using a hexose sugar as sole source of carbon in a minimal mineral medium. As a result of this metabolic evolution, the microbial organism acquires the ability to use pentose sugars derived from cellulosic materials for its growth while retaining the original growth kinetics, the rate of organic acid production and the ability to use hexose sugars as a source of carbon. This invention also discloses the genetic change in the microorganism that confers the ability to use both the hexose and pentose sugars simultaneously in the production of commercially significant quantities of organic acids.

Grabar, Tammy; Gong, Wei; Yocum, R Rogers

2014-10-28T23:59:59.000Z

453

Contribution of bacterial cells to lacustrine organic matter based on amino sugars and D-amino acids  

E-Print Network [OSTI]

is processed through the microbial loop (Ducklow, 2000). Fresh OM has high carbon-normalized yields of amino to the ASs, highest carbon normalized D-AA concentrations were found in the upper water column. For Lake Brienz 0.2­14% of the organic carbon pool originated from bacterial cells, compared to only 0

Wehrli, Bernhard

454

Introduction Riftia pachyptila (hereafter referred to solely as Riftia) is a  

E-Print Network [OSTI]

ingest particulate organic matter, and flourishes where dissolved organic carbon and nitrogen-time scales (Johnson et al., 1986; Johnson et al., 1988), with dissolved inorganic carbon concentrations at The hydrothermal vent tubeworm Riftia pachyptila is a dominant member of many hydrothermal vent communities along

Girguis, Peter R.

455

.RIFTBASINS OF THE PASSIVE MARGIN: TECTONICS, ORGANIC-RICH LACUSTRINE SEDIMENTS, BASIN ANALYSES  

E-Print Network [OSTI]

of the basin, organic-rich deep-water lacustrine sediments provide the source for the hydro- carbons. Organic, characterize these beds. Like the Green River Shales, micro- laminated sediment with well-pre- served whole). These organic- rich micro-laminated sediments are the result of depressed ecological efficiency in enormous

Olsen, Paul E.

456

Reinforced Carbon Nanotubes.  

DOE Patents [OSTI]

The present invention relates generally to reinforced carbon nanotubes, and more particularly to reinforced carbon nanotubes having a plurality of microparticulate carbide or oxide materials formed substantially on the surface of such reinforced carbon nanotubes composite materials. In particular, the present invention provides reinforced carbon nanotubes (CNTs) having a plurality of boron carbide nanolumps formed substantially on a surface of the reinforced CNTs that provide a reinforcing effect on CNTs, enabling their use as effective reinforcing fillers for matrix materials to give high-strength composites. The present invention also provides methods for producing such carbide reinforced CNTs.

Ren, Zhifen (Newton, MA); Wen, Jian Guo (Newton, MA); Lao, Jing Y. (Chestnut Hill, MA); Li, Wenzhi (Brookline, MA)

2005-06-28T23:59:59.000Z

457

Carbon Fiber SMC  

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

110,000 ACC capital) in 2008 * 54,000 for 2009 Partners * Continental Structural Plastic (CSP), a Tier One supplier * Discounted compounding and molding * Zoltek, a carbon...

458

Activated Carbon Injection  

SciTech Connect (OSTI)

History of the Clean Air Act and how the injection of carbon into a coal power plant's flu smoke can reduce the amount of mercury in the smoke.

None

2014-07-16T23:59:59.000Z

459

Activated Carbon Injection  

ScienceCinema (OSTI)

History of the Clean Air Act and how the injection of carbon into a coal power plant's flu smoke can reduce the amount of mercury in the smoke.

None

2014-07-22T23:59:59.000Z

460

Polaron spin current transport in organic semiconductors  

E-Print Network [OSTI]

of their unique functional properties, such as a long spin life- time that reflects their light-atom, mainly carbon-based composition. To date, the focus in organic spintronics has mainly been on studies of spin valves with a thin organic semicon- ductor layer... was extracted by fitting the measured field dependence of the voltage using symmetric and asymmetric Lorentz-type functions. A constant offset voltage due to the microwave irradiation (typically ? 100 nV) was also subtracted. g The equivalent circuit...

Watanabe, Shun; Ando, Kazuya; Kang, Keehoon; Mooser, Sebastian; Vaynzof, Yana; Kurebayashi, Hidekazu; Saitoh, Eiji; Sirringhaus, Henning

2014-03-16T23:59:59.000Z

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


461

EMBODIED CARBON TARIFFS Christoph Bhringer  

E-Print Network [OSTI]

EMBODIED CARBON TARIFFS Christoph Böhringer Jared C. Carbone Thomas F. Rutherford Revised: August 2013 Abstract Embodied carbon tariffs tax the direct and indirect carbon emissions embodied in trade -- an idea popularized by countries seeking to extend the reach of domestic carbon regu- lations. We

462

BIG SKY CARBON SEQUESTRATION PARTNERSHIP  

SciTech Connect (OSTI)

The Big Sky Carbon Sequestration Partnership, led by Montana State University, is comprised of research institutions, public entities and private sectors organizations, and the Confederated Salish and Kootenai Tribes and the Nez Perce Tribe. Efforts under this Partnership fall into four areas: evaluation of sources and carbon sequestration sinks; development of GIS-based reporting framework; designing an integrated suite of monitoring, measuring, and verification technologies; and initiating a comprehensive education and outreach program. At the first two Partnership meetings the groundwork was put in place to provide an assessment of capture and storage capabilities for CO{sub 2} utilizing the resources found in the Partnership region (both geological and terrestrial sinks), that would complement the ongoing DOE research. During the third quarter, planning efforts are underway for the next Partnership meeting which will showcase the architecture of the GIS framework and initial results for sources and sinks, discuss the methods and analysis underway for assessing geological and terrestrial sequestration potentials. The meeting will conclude with an ASME workshop. The region has a diverse array of geological formations that could provide storage options for carbon in one or more of its three states. Likewise, initial estimates of terrestrial sinks indicate a vast potential for increasing and maintaining soil C on forested, agricultural, and reclaimed lands. Both options include the potential for offsetting economic benefits to industry and society. Steps have been taken to assure that the GIS-based framework is consistent among types of sinks within the Big Sky Partnership area and with the efforts of other western DOE partnerships. Efforts are also being made to find funding to include Wyoming in the coverage areas for both geological and terrestrial sinks and sources. The Partnership recognizes the critical importance of measurement, monitoring, and verification technologies to support not only carbon trading but all policies and programs that DOE and other agencies may want to pursue in support of GHG mitigation. The efforts begun in developing and implementing MMV technologies for geological sequestration reflect this concern. Research is also underway to identify and validate best management practices for soil C in the Partnership region, and to design a risk/cost effectiveness framework to make comparative assessments of each viable sink, taking into account economic costs, offsetting benefits, scale of sequestration opportunities, spatial and time dimensions, environmental risks, and long-term viability. Scientifically sound information on MMV is critical for public acceptance of these technologies. Two key deliverables were completed in the second quarter--a literature review/database to assess the soil carbon on rangelands, and the draft protocols, contracting options for soil carbon trading. The protocols developed for soil carbon trading are unique and provide a key component of the mechanisms that might be used to efficiently sequester GHG and reduce CO{sub 2} concentrations. While no key deliverables were due during the third quarter, progress on other deliverables is noted in the PowerPoint presentations and in this report. A series of meetings held during the second and third quarters have laid the foundations for assessing the issues surrounding carbon sequestration in this region, the need for a holistic approach to meeting energy demands and economic development potential, and the implementation of government programs or a market-based setting for soil C credits. These meetings provide a connection to stakeholders in the region and a basis on which to draw for the DOE PEIS hearings. In the fourth quarter, three deliverables have been completed, some in draft form to be revised and updated to include Wyoming. This is due primarily to some delays in funding to LANL and INEEL and the approval of a supplemental proposal to include Wyoming in much of the GIS data sets, analysis, and related materials. The de

Susan M. Capalbo

2004-10-31T23:59:59.000Z

463

Big Sky Carbon Sequestration Partnership  

SciTech Connect (OSTI)

The Big Sky Carbon Sequestration Partnership, led by Montana State University, is comprised of research institutions, public entities and private sectors organizations, and the Confederated Salish and Kootenai Tribes and the Nez Perce Tribe. Efforts under this Partnership in Phase I fall into four areas: evaluation of sources and carbon sequestration sinks that will be used to determine the location of pilot demonstrations in Phase II; development of GIS-based reporting framework that links with national networks; designing an integrated suite of monitoring, measuring, and verification technologies and assessment frameworks; and initiating a comprehensive education and outreach program. The groundwork is in place to provide an assessment of storage capabilities for CO2 utilizing the resources found in the Partnership region (both geological and terrestrial sinks), that would complement the ongoing DOE research agenda in Carbon Sequestration. The region has a diverse array of geological formations that could provide storage options for carbon in one or more of its three states. Likewise, initial estimates of terrestrial sinks indicate a vast potential for increasing and maintaining soil C on forested, agricultural, and reclaimed lands. Both options include the potential for offsetting economic benefits to industry and society. Steps have been taken to assure that the GIS-based framework is consistent among types of sinks within the Big Sky Partnership area and with the efforts of other DOE regional partnerships. The Partnership recognizes the critical importance of measurement, monitoring, and verification technologies to support not only carbon trading but all policies and programs that DOE and other agencies may want to pursue in support of GHG mitigation. The efforts in developing and implementing MMV technologies for geological sequestration reflect this concern. Research is also underway to identify and validate best management practices for soil C in the Partnership region, and to design a risk/cost effectiveness framework to make comparative assessments of each viable sink, taking into account economic costs, offsetting benefits, scale of sequestration opportunities, spatial and time dimensions, environmental risks, and long-term viability. Scientifically sound MMV is critical for public acceptance of these technologies. Deliverables for the 7th Quarter reporting period include (1) for the geological efforts: Reports on Technology Needs and Action Plan on the Evaluation of Geological Sinks and Pilot Project Deployment (Deliverables 2 and 3), and Report on the Feasibility of Mineralization Trapping in the Snake River Plain Basin (Deliverable 14); (2) for the terrestrial efforts: Report on the Evaluation of Terrestrial Sinks and a Report of the Best Production Practices for Soil C Sequestration (Deliverables 8 and 15). In addition, the 7th Quarter activities for the Partnership included further development of the proposed activities for the deployment and demonstration phase of the carbon sequestration pilots including geological and terrestrial pilots, expansion of the Partnership to encompass regions and institutions that are complimentary to the steps we have identified, building greater collaborations with industry and stakeholders in the region, contributed to outreach efforts that spanned all partnerships, co-authorship on the Carbon Capture and Separation report, and developed a regional basis to address future energy opportunities in the region. The deliverables and activities are discussed in the following sections and appended to this report. The education and outreach efforts have resulted in a comprehensive plan which serves as a guide for implementing the outreach activities under Phase I. The public website has been expanded and integrated with the GIS carbon atlas. We have made presentations to stakeholders and policy makers including two tribal sequestration workshops, and made connections to other federal and state agencies concerned with GHG emissions, climate change, and efficient and environmental

Susan M. Capalbo

2005-11-01T23:59:59.000Z

464

Dissolved methane distributions and air-sea flux in the plume of a massive seep field, Coal Oil Point, California  

E-Print Network [OSTI]

Dissolved methane distributions and air-sea flux in the plume of a massive seep field, Coal Oil coastal ocean near Coal Oil Point, Santa Barbara Channel, California. Methane was quantified in the down current surface water at 79 stations in a 280 km2 study area. The methane plume spread over an area of $70

Washburn, Libe

465

Reversing Climate Change: Using Carbon Technology to Offset Carbon Emissions  

E-Print Network [OSTI]

Reversing Climate Change: Using Carbon Technology to Offset Carbon Emissions Climate change is real not only emitting less greenhouse gas (GHG), but actually sources of negative carbon. We then present two

466

Carbon-Optimal and Carbon-Neutral Supply Chains  

E-Print Network [OSTI]

Y. Li, M. Daskin. 2009. Carbon Footprint and the ManagementJ. van Houtum. 2011. E?ect of carbon emission regulations onStreamlined Enterprise Carbon Footprinting. Environmental

Caro, F.; Corbett, C. J.; Tan, T.; Zuidwijk, R.

2011-01-01T23:59:59.000Z

467

Electrochemical behavior of carbon aerogels derived from different precursors  

SciTech Connect (OSTI)

The ability to tailor the structure and properties of porous carbons has led to their increased use as electrodes in energy storage devices. Our research focuses on the synthesis and characterization of carbon aerogels for use in electrochemical double layer capacitors. Carbon aerogels are formed from the sol-gel polymerization of (1) resorcinol-formaldehyde or (2) phenolic-furfural, followed by supercritical drying from carbon dioxide, and subsequent pyrolysis in an inert atmosphere. These materials can be produced as monoliths, composites, thin films, powders, or microspheres. In all cases, the areogels have an open-cell structure with an ultrafine pore size (<100 nm), high surface area (400-1 100 m{sup 2}/g), and a solid matrix composed of interconnected particles, fibers, or platelets with characteristic dimensions of 10 nm. This paper examines the effects of the carbon precursor and processing conditions on electrochemical performance in aqueous and organic electrolytes.

Pekala, R.W.; Alviso, C.T.; Nielson, J.K.; Tran, T.D. [Lawrence Livermore National Lab., CA (United States); Reynolds, G.M.; Dresshaus, M.S. [Massachusetts Inst. of Tech., Cambridge, MA (United States). Dept. of Physics

1995-04-01T23:59:59.000Z

468

Glossary of Volatile Organic Compounds Ethylbenzene Carbon tetrachloride  

E-Print Network [OSTI]

;Ethylbenzene Ethylbenzene is a colorless, flammable liquid found in natural products such as coal tar and petroleum. It is also found in manufactured products such as inks, insecticides, and paints. Ethylbenzene in the air. In surface water, ethylbenzene breaks down by reacting with other chemicals found naturally

469

River delta sediments account for ~44% of organic carbon  

E-Print Network [OSTI]

. 2006 C) "Photodissolution" of POC from deltaic sediments during simulated solar irradiation OR CO2 CO2 of enzymes to THAA, suggesting that the initial drop was due to protein "encapsulation" by protective

Boss, Emmanuel S.

470

Metal-Organic Frameworks with Precisely Designed Interior for Carbon  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary)morphinanInformation Desert Southwest Regionat Cornell Batteries & Fuel Cells InDioxide Capture in the

471

Metal-Organic Frameworks with Precisely Designed Interior for Carbon  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr May Jun Jul(Summary)morphinanInformation Desert Southwest Regionat Cornell Batteries & Fuel Cells InDioxide Capture in

472

Metal Organic Clathrates for Carbon Dioxide Removal - Energy Innovation  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE:1 First Use of Energy for All Purposes (Fuel and Nonfuel),Feet) Year Jan Feb Mar Apr MayAtmospheric Optical Depth7-1D: VegetationEquipment Surfaces andMapping theEnergy StorageAdvanced Materials Advanced

473

assimilable organic carbon: Topics by E-print Network  

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

A COUPLED ATMOSPHERE- Engineering Websites Summary: to best estimate CO2 fluxes on the Earths surface by assimilating observations of atmospheric CO2 to transport atmospheric...

474

The effects of total dissolved gas on chum salmon fry survival, growth, gas bubble disease, and seawater tolerance  

SciTech Connect (OSTI)

Chum salmon Oncorhynchus keta alevin developing in gravel habitats downstream of Bonneville Dam on the Columbia River are exposed to elevated levels of total dissolved gas (TDG) when water is spilled at the dam to move migrating salmon smolts downstream to the Pacific Ocean. Current water quality criteria for the management of dissolved gas in dam tailwaters were developed primarily to protect salmonid smolts and are assumed to be protective of alevin if adequate depth compensation is provided. We studied whether chum salmon alevin exposed to six levels of dissolved gas ranging from 100% to 130% TDG at three development periods between hatch and emergence (hereafter early, middle, and late stage) suffered differential mortality, growth, gas bubble disease, or seawater tolerance. Each life stage was exposed for 50 d (early stage), 29 d (middle stage), or 16 d (late stage) beginning at 13, 34, and 37 d post-hatch, respectively, through 50% emergence. The mortality for all stages from exposure to emergence was estimated to be 8% (95% confidence interval (CI) of 4% to 12%) when dissolved gas levels were between 100% and 117% TDG. Mortality significantly increased as dissolved gas levels rose above 117% TDG,; with the lethal concentration that produced 50% mortality (LC50 ) was estimated to be 128.7% TDG (95% CI of 127.2% to 130.2% TDG) in the early and middle stages. By contrast, there was no evidence that dissolved gas level significantly affected growth in any life stage except that the mean wet weight at emergence of early stage fish exposed to 130% TDG was significantly less than the modeled growth of unexposed fish. The proportion of fish afflicted with gas bubble disease increased with increasing gas concentrations and occurred most commonly in the nares and gastrointestinal tract. Early stage fish exhibited higher ratios of filament to lamellar gill chloride cells than late stage fish, and these ratios increased and decreased for early and late stage fish, respectively, as gas levels increased; however, there were no significant differences in mortality between life stages after 96 h in seawater. The study results suggest that current water quality guidelines for the management of dissolved gas appear to offer a conservative level of protection to chum salmon alevin incubating in gravel habitat downstream of Bonneville Dam.

Geist, David R.; Linley, Timothy J.; Cullinan, Valerie I.; Deng, Zhiqun

2013-02-01T23:59:59.000Z

475

DEVELOPMENT OF CONTINUOUS SOLVENT EXTRACTION PROCESSES FOR COAL DERIVED CARBON PRODUCTS  

SciTech Connect (OSTI)

The purpose of this DOE-funded effort is to develop continuous processes for solvent extraction of coal for the production of carbon products. These carbon products include materials used in metals smelting, especially in the aluminum and steel industries, as well as porous carbon structural material referred to as ''carbon foam'' and carbon fibers. A process has been developed which results in high quality binder pitch suitable for use in graphite electrodes or carbon anodes. A detailed description of the protocol is given by Clendenin. Briefly, aromatic heavy oils are hydro-treated under mild conditions in order to increase their ability to dissolve coal. An example of an aromatic heavy oil is Koppers Carbon Black Base (CBB) oil. CBB oil has been found to be an effective solvent and acceptably low cost (i.e., significantly below the market price for binder pitch, or about $280 per ton at the time of this writing). It is also possible to use solvents derived from hydrotreated coal and avoid reliance on coke oven recovery products completely if so desired.

Elliot B. Kennel; Philip L. Biedler; Chong Chen; Dady Dadyburjor; Liviu Magean; Peter G. Stansberry; Alfred H. Stiller; John W. Zondlo

2005-04-13T23:59:59.000Z

476

Electrochemical formation of hydroxide for enhancing carbon dioxide and acid gas uptake by a solution  

DOE Patents [OSTI]

A system for forming metal hydroxide from a metal carbonate utilizes a water electrolysis cell having an acid-producing anode and a hydroxyl-producing cathode immersed in a water solution of sufficient ionic content to allow an electric current to pass between the hydroxyl-producing cathode and the acid-producing anode. A metal carbonate is placed in close proximity to the acid-producing anode. A direct current electrical voltage is provided across the acid-producing anode and the hydroxyl-producing cathode sufficient to generate acid at the acid-producing anode and hydroxyl ions at the hydroxyl-producing cathode. The acid dissolves at least part of the metal carbonate into metal and carbonate ions allowing the metal ions to travel toward the hydroxyl-producing cathode and to combine with the hydroxyl ions to form the metal hydroxide. The carbonate ions travel toward the acid-producing anode and form carbonic acid and/or water and carbon dioxide.

Rau, Gregory Hudson

2014-07-01T23:59:59.000Z

477

Carbon-Optimal and Carbon-Neutral Supply Chains  

E-Print Network [OSTI]

Pearce, D. 2003. The Social Cost Of Carbon And Its PolicyR.S.J. 2008. The Social Cost of Carbon: Trends, Outliers and

Caro, F.; Corbett, C. J.; Tan, T.; Zuidwijk, R.

2011-01-01T23:59:59.000Z

478

Carbonation Mechanism of Reservoir Rock by Supercritical Carbon...  

Open Energy Info (EERE)

from reservoir rock formation. - Task 2: Carbonation study of minerals. - Task 3: Mechanical behaviors of carbonated minerals. - Task 4: Modeling of CO2- reservoir rock...

479

Effective Permeability Change in Wellbore Cement with Carbon Dioxide Reaction  

SciTech Connect (OSTI)

Portland cement, a common sealing material for wellbores for geological carbon sequestration was reacted with CO{sub 2} in supercritical, gaseous, and aqueous phases at various pressure and temperature conditions to simulate cement-CO{sub 2} reaction along the wellbore from carbon injection depth to the near-surface. Hydrated Portland cement columns (14 mm diameter x 90 mm length; water-to-cement ratio = 0.33) including additives such as steel coupons and Wallula basalt fragments were reacted with CO{sub 2} in the wet supercritical (the top half) and dissolved (the bottom half) phases under carbon sequestration condition with high pressure (10 MPa) and temperature (50 C) for 5 months, while small-sized hydrated Portland cement columns (7 mm diameter x 20 mm length; water-to-cement ratio = 0.38) were reacted with CO{sub 2} in dissolved phase at high pressure (10 MPa) and temperature (50 C) for 1 month or with wet CO{sub 2} in gaseous phase at low pressure (0.2 MPa) and temperature (20 C) for 3 months. XMT images reveal that the cement reacted with CO{sub 2} saturated groundwater had degradation depth of {approx}1 mm for 1 month and {approx}3.5 mm for 5 month, whereas the degradation was minor with cement exposure to supercritical CO{sub 2}. SEM-EDS analysis showed that the carbonated cement was comprised of three distinct zones; the innermost less degraded zone with Ca atom % > C atom %, the inner degraded zone with Ca atom % {approx} C atom % due to precipitation of calcite, the outer degraded zone with C atom % > Ca atom % due to dissolution of calcite and C-S-H, as well as adsorption of carbon to cement matrix. The outer degraded zone of carbonated cement was porous and fractured because of dissolution-dominated reaction by carbonic acid exposure, which resulted in the increase in BJH pore volume and BET surface area. In contrast, cement-wet CO{sub 2}(g) reaction at low P (0.2 MPa)-T (20 C) conditions for 1 to 3 months was dominated by precipitation of micron-sized calcite on the outside surface of cement, which resulted in the decrease in BJH pore volume and BET surface area. Cement carbonation and pore structure change are significantly dependent on pressure and temperature conditions as well as the phase of CO{sub 2}, which controls the balance between precipitation and dissolution in cement matrix. Geochemical modeling result suggests that ratio of solid (cement)-to-solution (carbonated water) has a significant effect on cement carbonation, thus the cement-CO{sub 2} reaction experiment needs to be conducted under realistic conditions representing the in-situ wellbore environment of carbon sequestration field site. Total porosity and air permeability for a duplicate cement column with water-to-cement ratio of 0.38 measured after oven-drying by Core Laboratories using Boyle's Law technique and steady-state method were 31% and 0.576 mD. A novel method to measure the effective liquid permeability of a cement column using X-ray micro-tomography images after injection of pressurized KI (potassium iodide) is under development by PNNL. Preliminary results indicate the permeability of a cement column with water-to-cement ratio of 0.38 is 4-8 mD. PNNL will apply the method to understand the effective permeability change of Portland cement by CO{sub 2}(g) reaction under a variety of pressure and temperature conditions to develop a more reliable well-bore leakage risk model.

Um, Wooyong; Jung, Hun Bok; Martin, Paul F.; McGrail, B. Peter

2011-11-01T23:59:59.000Z

480

Carbon monoxide absorbing liquid  

SciTech Connect (OSTI)

The present disclosure is directed to a carbon monoxide absorbing liquid containing a cuprous ion, hydrochloric acid and titanum trichloride. Titanium trichloride is effective in increasing the carbon monoxide absorption quantity. Furthermore, titanium trichloride remarkably increases the oxygen resistance. Therefore, this absorbing liquid can be used continuously and for a long time.

Arikawa, Y.; Horigome, S.; Kanehori, K.; Katsumoto, M.

1981-07-07T23:59:59.000Z

Note: This page contains sample records for the topic "dissolved organic carbon" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
to obtain the most current and comprehensive results.


481

Fly ash carbon passivation  

DOE Patents [OSTI]

A thermal method to passivate the carbon and/or other components in fly ash significantly decreases adsorption. The passivated carbon remains in the fly ash. Heating the fly ash to about 500 and 800 degrees C. under inert gas conditions sharply decreases the amount of surfactant adsorbed by the fly ash recovered after thermal treatment despite the fact that the carbon content remains in the fly ash. Using oxygen and inert gas mixtures, the present invention shows that a thermal treatment to about 500 degrees C. also sharply decreases the surfactant adsorption of the recovered fly ash even though most of the carbon remains intact. Also, thermal treatment to about 800 degrees C. under these same oxidative conditions shows a sharp decrease in surfactant adsorption of the recovered fly ash due to the fact that the carbon has been removed. This experiment simulates the various "carbon burnout" methods and is not a claim in this method. The present invention provides a thermal method of deactivating high carbon fly ash toward adsorption of AEAs while retaining the fly ash carbon. The fly ash can be used, for example, as a partial Portland cement replacement in air-entrained concrete, in conductive and other concretes, and for other applications.

La Count, Robert B; Baltrus, John P; Kern, Douglas G

2013-05-14T23:59:59.000Z

482

Electronic Properties of Carbon Nanotubes  

E-Print Network [OSTI]

P. Avouris, in Carbon Nanotubes M. S. Dresselhaus, P.Physics of Carbon Nanotubes S. V. Rotkin, S. Subramoney,Properties of Carbon Nanotubes Philip G. Collins 1 and

Collins, Philip G

2008-01-01T23:59:59.000Z

483

Carbon Park Environmental Impact Assessment  

E-Print Network [OSTI]

of offsetting the University's carbon footprint, promoting biodiversity and establishing easily maintained Carbon Park Environmental Impact Assessment A B.E.S.T. Project By, Adam Bond 2011 #12; Bishop's University Carbon Park

484

Electronic Properties of Carbon Nanotubes  

E-Print Network [OSTI]

P. Avouris, in Carbon Nanotubes M. S. Dresselhaus, P.in Applied Physics of Carbon Nanotubes S. V. Rotkin, S.Electronic Properties of Carbon Nanotubes Philip G. Collins

Collins, Philip G

2008-01-01T23:59:59.000Z

485

Dissolved and particulate aluminum in the Columbia River and coastal waters of Oregon and Washington: behavior in near-field and far-field plumes  

E-Print Network [OSTI]

1 Dissolved and particulate aluminum in the Columbia River and coastal waters of Oregon) and particulate (leachable and total) aluminum was examined in the Columbia River and estuary, in near Influence on Shelf Ecosystems (RISE) cruise of May/June 2006. Dissolved and particulate aluminum (Al

Hickey, Barbara

486

Organic Photovoltaics Philip Schulz  

E-Print Network [OSTI]

Field Effect Transistors Organic Light Emitting Diodes Organic Solar Cells .OFET, OTFT .RF-ID tag 1977 ­ Conductivity in polymers 1986 ­ First heterojunction OPV 1987 ­ First organic light emitting diode (OLED) 1993 ­ First OPV from solution processing 2001 ­ First certified organic solar cell with 2

Firestone, Jeremy

487

Departmental Organization and Management  

Broader source: Directives, Delegations, and Requirements [Office of Management (MA)]

Effective immediately, the Departmental organization structure reflected in the chart at Attachment 1 has been approved.

1993-06-10T23:59:59.000Z

488

Dissolved cadmium in the Southern Ocean: Distribution, speciation, and relation to phosphate  

E-Print Network [OSTI]

is insignificant, and removed by physical adsorption and biological uptake by microorgan- isms (Bruland 1980). Cd to strong organic ligands in surface waters (Bruland 1992; Sunda and Huntsman 2000; Ellwood 2004

Boyer, Edmond

489

Fiber-based adsorbents having high adsorption capacities for recovering dissolved metals and methods thereof  

DOE Patents [OSTI]

A fiber-based adsorbent and a related method of manufacture are provided. The fiber-based adsorbent includes polymer fibers with grafted side chains and an increased surface area per unit weight over known fibers to increase the adsorption of dissolved metals, for example uranium, from aqueous solutions. The polymer fibers include a circular morphology in some embodiments, having a mean diameter of less than 15 microns, optionally less than about 1 micron. In other embodiments, the polymer fibers include a non-circular morphology, optionally defining multiple gear-shaped, winged-shaped or lobe-shaped projections along the length of the polymer fibers. A method for forming the fiber-based adsorbents includes irradiating high surface area polymer fibers, grafting with polymerizable reactive monomers, reacting the grafted fibers with hydroxylamine, and conditioning with an alkaline solution. High surface area fiber-based adsorbents formed according to the present method demonstrated a significantly improved uranium adsorption capacity per unit weight over existing adsorbents.

Janke, Christopher J; Dai, Sheng; Oyola, Yatsandra

2014-05-13T23:59:59.000Z

490

Prediction of Total Dissolved Gas (TDG) at Hydropower Dams throughout the Columbia  

SciTech Connect (OSTI)

The network of dams throughout the Columbia River Basin (CRB) are managed for irrigation, hydropower production, flood control, navigation, and fish passage that frequently result in both voluntary and involuntary spillway releases. The entrainment of air in spillway releases and the subsequent exchange of atmospheric gasses into solution during passage through the stilling basin cause elevated levels of total dissolved gas (TDG) saturation. Physical processes that affect TDG exchange at hydropower facilities have been characterized throughout the CRB in site-specific studies and at real-time water quality monitoring stations. These data have been used to develop predictive models of TDG exchange which are site specific and account for the fate of spillway and powerhouse flows in the tailrace channel and resultant transport and exchange in route to the downstream dam. Currently, there exists a need to summarize the findings from operational and structural TDG abatement programs conducted throughout the CRB and for the development of a generalized prediction model that pools data collected at multiple projects with similar structural attributes. A generalized TDG exchange model can be tuned to specific projects and coupled with water regulation models to allow for the formulation of optimal water regulation schedules subject to water quality constraints for TDG supersaturation. It is proposed to develop a methodology for predicting TDG levels downstream of hydropower facilities with similar structural properties as a function of a set of variables that affect TDG exchange; such as tailwater depth, spill discharge and pattern, project head, and entrainment of powerhouse releases.

Pasha, MD Fayzul K [ORNL] [ORNL; Hadjerioua, Boualem [ORNL] [ORNL; Stewart, Kevin M [ORNL] [ORNL; Bender, Merlynn [Bureau of Reclamation] [Bureau of Reclamation; Schneider, Michael L. [U.S. Army Corps of Engineers] [U.S. Army Corps of Engineers

2012-01-01T23:59:59.000Z

491

The effect of Sequoyah Nuclear Plant on dissolved oxygen in Chickamauga Reservoir  

SciTech Connect (OSTI)

During the summer of 1985, the Tennessee Division of Water Pollution Control and the Tennessee Wildlife Resources Agency measured dissolved oxygen (DO) concentrations downstream from the Sequoyah Nuclear Plant (SQN) discharge mixing zone that were below the state criterion for DO. The Tennessee General Water Quality Criteria'' specifies that DO should be a minimum of 5.0 mg/l measured at a depth of 5 feet for the protection of fish and aquatic life. The Tennessee Valley Authority developed the present study to answer general concerns about reservoir conditions and potential for adverse effects on aquatic biota. Four objectives were defined for this study: (1) to better define the extent and duration of the redistribution of DO in the reservoir, (2) to better understand DO dynamics within the mixing zone, (3) to determine whether DO is being lost (or added) as the condenser cooling water passes through the plant, and (4) to evaluate the potential for impact on aquatic life in the reservoir.

Butkus, S.R.; Shiao, M.C.; Yeager, B.L.

1990-09-01T23:59:59.000Z

492

Pacific Northwest rangeland carbon sequestration.  

E-Print Network [OSTI]

??This paper models the supply curve of carbon sequestration on Pacific Northwest rangelands. Rangeland managers have the ability to sequester carbon in agricultural soils by… (more)

Wiggins, Seth T.

2012-01-01T23:59:59.000Z

493

CARBON SEQUESTRATION STRATEGIES FOR CALIFORNIA  

E-Print Network [OSTI]

GEOLOGIC CARBON SEQUESTRATION STRATEGIES FOR CALIFORNIA: REPORT TO THE LEGISLATURE Regional Carbon Sequestration Partnership (WESTCARB) studies that we used, including Cameron Downey

494

BIG SKY CARBON SEQUESTRATION PARTNERSHIP  

SciTech Connect (OSTI)

The Big Sky Partnership, led by Montana State University, is comprised of research institutions, public entities and private sectors organizations, and the Confederated Salish and Kootenai Tribes and the Nez Perce Tribe. Efforts during the second performance period fall into four areas: evaluation of sources and carbon sequestration sinks; development of GIS-based reporting framework; designing an integrated suite of monitoring, measuring, and verification technologies; and initiating a comprehensive education and outreach program. At the first two Partnership meetings the groundwork was put in place to provide an assessment of capture and storage capabilities for CO{sub 2} utilizing the resources found in the Partnership region (both geological and terrestrial sinks), that would complement the ongoing DOE research. The region has a diverse array of geological formations that could provide storage options for carbon in one or more of its three states. Likewise, initial estimates of terrestrial sinks indicate a vast potential for increasing and maintaining soil C on forested, agricultural, and reclaimed lands. Both options include the potential for offsetting economic benefits to industry and society. Steps have been taken to assure that the GIS-based framework is consistent among types of sinks within the Big Sky Partnership area and with the efforts of other western DOE partnerships. Efforts are also being made to find funding to include Wyoming in the coverage areas for both geological and terrestrial sinks and sources. The Partnership recognizes the critical importance of measurement, monitoring, and verification technologies to support not only carbon trading but all policies and programs that DOE and other agencies may want to pursue in support of GHG mitigation. The efforts begun in developing and implementing MMV technologies for geological sequestration reflect this concern. Research is also underway to identify and validate best management practices for soil C in the partnership region, and to design a risk/cost effectiveness framework to make comparative assessments of each viable sink, taking into account economic costs, offsetting benefits, scale of sequestration opportunities, spatial and time dimensions, environmental risks, and long term viability. Scientifically sound information on MMV is critical for public acceptance of these technologies. Two key deliverables were completed this quarter--a literature review/database to assess the soil carbon on rangelands, and the draft protocols, contracting options for soil carbon trading. To date, there has been little research on soil carbon on rangelands, and since rangeland constitutes a major land use in the Big Sky region, this is important in achieving a better understanding of terrestrial sinks. The protocols developed for soil carbon trading are unique and provide a key component of the mechanisms that might be used to efficiently sequester GHG and reduce CO{sub 2} concentrations. Progress on other deliverables is noted in the PowerPoint presentations. A series of meetings held during the second quarter have laid the foundations for assessing the issues surrounding the implementation of a market-based setting for soil C credits. These meetings provide a connection to stakeholders in the region and a basis on which to draw for the DOE PEIS hearings. Finally, the education and outreach efforts have resulted in a comprehensive plan and process which serves as a guide for implementing the outreach activities under Phase I. While we are still working on the public website, we have made many presentations to stakeholders and policy makers, connections to other federal and state agencies concerned with GHG emissions, climate change, and efficient and environmentally-friendly energy production. In addition, we have laid plans for integration of our outreach efforts with the students, especially at the tribal colleges and at the universities involved in our partnership. This includes collaboration with the film and media arts departments at MSU, with outreach effort

Susan M. Capalbo

2004-06-01T23:59:59.000Z

495

Big Sky Carbon Sequestration Partnership  

SciTech Connect (OSTI)

The Big Sky Carbon Sequestration Partnership, led by Montana State University, is comprised of research institutions, public entities and private sectors organizations, and the Confederated Salish and Kootenai Tribes and the Nez Perce Tribe. Efforts under this Partnership in Phase I are organized into four areas: (1) Evaluation of sources and carbon sequestration sinks that will be used to determine the location of pilot demonstrations in Phase II; (2) Development of GIS-based reporting framework that links with national networks; (3) Design of an integrated suite of monitoring, measuring, and verification technologies, market-based opportunities for carbon management, and an economic/risk assessment framework; (referred to below as the Advanced Concepts component of the Phase I efforts) and (4) Initiation of a comprehensive education and outreach program. As a result of the Phase I activities, the groundwork is in place to provide an assessment of storage capabilities for CO{sub 2} utilizing the resources found in the Partnership region (both geological and terrestrial sinks), that complements the ongoing DOE research agenda in Carbon Sequestration. The geology of the Big Sky Carbon Sequestration Partnership Region is favorable for the potential sequestration of enormous volume of CO{sub 2}. The United States Geological Survey (USGS 1995) identified 10 geologic provinces and 111 plays in the region. These provinces and plays include both sedimentary rock types characteristic of oil, gas, and coal productions as well as large areas of mafic volcanic rocks. Of the 10 provinces and 111 plays, 1 province and 4 plays are located within Idaho. The remaining 9 provinces and 107 plays are dominated by sedimentary rocks and located in the states of Montana and Wyoming. The potential sequestration capacity of the 9 sedimentary provinces within the region ranges from 25,000 to almost 900,000 million metric tons of CO{sub 2}. Overall every sedimentary formation investigated has significant potential to sequester large amounts of CO{sub 2}. Simulations conducted to evaluate mineral trapping potential of mafic volcanic rock formations located in the Idaho province suggest that supercritical CO{sub 2} is converted to solid carbonate mineral within a few hundred years and permanently entombs the carbon. Although MMV for this rock type may be challenging, a carefully chosen combination of geophysical and geochemical techniques should allow assessment of the fate of CO{sub 2} in deep basalt hosted aquifers. Terrestrial carbon sequestration relies on land management practices and technologies to remove atmospheric CO{sub 2} where it is stored in trees, plants, and soil. This indirect sequestration can be implemented today and is on the front line of voluntary, market-based approaches to reduce CO{sub 2} emissions. Initial estimates of terrestrial sinks indicate a vast potential for increasing and maintaining soil Carbon (C) on rangelands, and forested, agricultural, and reclaimed lands. Rangelands can store up to an additional 0.05 mt C/ha/yr, while the croplands are on average four times that amount. Estimates of technical potential for soil sequestration within the region in cropland are in the range of 2.0 M mt C/yr over 20 year time horizon. This is equivalent to approximately 7.0 M mt CO{sub 2}e/yr. The forestry sinks are well documented, and the potential in the Big Sky region ranges from 9-15 M mt CO{sub 2} equivalent per year. Value-added benefits include enhanced yields, reduced erosion, and increased wildlife habitat. Thus the terrestrial sinks provide a viable, environmentally beneficial, and relatively low cost sink that is available to sequester C in the current time frame. The Partnership recognizes the critical importance of measurement, monitoring, and verification technologies to support not only carbon trading but all policies and programs that DOE and other agencies may want to pursue in support of GHG mitigation. The efforts in developing and implementing MMV technologies for geological and terrestrial sequestration re

Susan Capalbo

2005-12-31T23:59:59.000Z

496

Biological control of vertical carbon flux in the California current and Equatorial Pacific  

E-Print Network [OSTI]

carbon to depth (e.g. Bruland and Silver 1981; Landry et al.flux of organic matter to the deep sea (Bruland and Silver1981; Silver and Bruland 1981; Pfannkuche and Lochte 1993).

Stukel, Michael Raymond

2011-01-01T23:59:59.000Z

497

Radiation Detection: Resistivity Responses in Functional Poly(Olefin Sulfone)/Carbon Nanotube Composites  

E-Print Network [OSTI]

Detection of gamma rays is shown using a non-scintillating organic-based sensor composed of poly(olefin sulfone)/carbon nanotube blends. Functionalization of the polymers can be performed after polymerization to tailor ...

Swager, Timothy Manning

498

Black carbon in marine sediments : quantification and implications for the sorption of polycyclic aromatic hydrocarbons  

E-Print Network [OSTI]

Sorption is a key factor in determining the fate of polycyclic aromatic hydrocarbons (PAHs) in the environment. Here, PAH sorption is proposed as the sum of two mechanisms: absorption into a biogenic, organic carbon (OC) ...

Accardi-Dey, AmyMarie, 1976-

2003-01-01T23:59:59.000Z

499

Molten carbonate fuel cell cathode with mixed oxide coating  

DOE Patents [OSTI]

A molten carbonate fuel cell cathode having a cathode body and a coating of a mixed oxygen ion conductor materials. The mixed oxygen ion conductor materials are formed from ceria or doped ceria, such as gadolinium doped ceria or yttrium doped ceria. The coating is deposited on the cathode body using a sol-gel process, which utilizes as precursors organometallic compounds, organic and inorganic salts, hydroxides or alkoxides and which uses as the solvent water, organic solvent or a mixture of same.

Hilmi, Abdelkader; Yuh, Chao-Yi

2013-05-07T23:59:59.000Z

500

Cumulative Carbon and Just Allocation of the Global Carbon Commons  

E-Print Network [OSTI]

Cumulative Carbon and Just Allocation of the Global Carbon Commons R.T. Pierrehumbert* Abstract statistic, called cumulative carbon. This statistic is the aggregate amount ofcarbon emitted in theform such activitiespersist.In thispaper the conceptis usedto addressthe question offair allocation of carbon emissions

Pierrehumbert, Raymond