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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

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

Evaluation of the Origin of Dissolved Organic Carbon and the Treatability of Mercury in Flue Gas Desulfurization Wastewater  

Science Conference Proceedings (OSTI)

Regulations for reducing the dissolved mercury (Hg) concentrations in wastewater discharged by electric generating power plants are becoming more stringent via federal regulatory limits proposed by the EPA and regulatory limits set by select states. Data obtained in a previous EPRI study conducted in 2009 suggested a potential negative impact of dissolved organic carbon (DOC) and iodide concentrations present in flue gas desulfurization (FGD) wastewater on mercury treatability (EPRI report 1019867). ...

2013-12-17T23:59:59.000Z

3

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

E-Print Network (OSTI)

The Bryan/College Station (B/CS) region has been reported to have elevated concentrations of dissolved organic carbon (DOC) in surface water. Increased DOC concentrations are worrisome as DOC has been shown to be an energy source for the recovery and regrowth of E. coli and many watersheds are impaired by high bacteria levels. To examine the sources and fates of DOC in rural and urban regions to better understand DOC movement though the environment, seven watersheds were studied. To investigate source, streams were analyzed using diffuse reflectance near infrared spectroscopy (DR-NIR) and carbon isotopes. Fate of DOC was determined through monthly streams samples, gathered between March 2011 and February 2012, which were incubated for biodegradable DOC (BDOC). Soil in the region was sampled based on land use categories. Soil was analyzed for DOC and BDOC as well as DOC adsorption, the other major fate of DOC. Above ground vegetation was sampled in conjunction with soil and analyzed for BDOC. Data indicated that fecal matter from cliff swallows provided considerable organic material to streams in the B/CS region as shown through DR-NIR. Carbon isotope values in streams ranged from -23.5 +/- 0.7% to -26.8 +/- 0.5%. Stream spectra may be able to predict carbon isotope values in streams (Adj. R2 = 0.88). Mean annual stream DOC concentrations ranged from 11 +/- 3 mg/L to 31 +/- 12 mg/L, which represents a significant decrease in DOC between 2007 and 2011. Concurrent increases in pH and conductivity were also recorded. The decrease in DOC and the increases in pH and conductivity may be due to impacts of high sodium irrigation tap water. Biodegradable DOC was low in streams, which is likely due to DOC being present in streams in refractory forms that are resistant to microbial breakdown. Soil chemistry, including soil adsorption, was greatly influenced by sodium. The elevated adsorption coefficients and release values seen in highly developed and urban open areas can be attributed 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 quality as a result of this research.

Cioce, Danielle

2012-08-01T23:59:59.000Z

4

Low dissolved organic carbon input from fresh litter to deep mineral soils  

SciTech Connect

Dissolved organic carbon (DOC) leached from recent litter in the forest floor has been suggested to be an important source of C to the mineral soil of forest ecosystems. In order to determine the rate at which this flux of C occurs we have taken advantage of a local release of 14C at Oak Ridge National Laboratory Reservation, USA (latitude N 35 58'; longitude W 84 16'). Eight replicate 7x7 m plots were estab lished at four field sites on the reservation in an upland oak forest setting. Half of the plots were provided with 14C-enriched litter (?14C ?1000 ), and the other half with near-background litter (?14C ?220 ) over multiple years. Differences in the labeled leaf litter were used to quantify the movement of litter derived DOC through the soil profile. Soil solutions were collected over several years with tension lysimeters at 15 and 70 cm depth and measured for DOC concentration and 14C abundance. The net amount of DOC retained between 15 and 70 cm was 1.5-6 g m-2 y-1. There were significant effects of the litter additions on the 14C abundance in the DOC, but the net transport of 14C from the added litter was small. The difference in ?14C between the treatments with enriched and near-background litter was only about 130 at both depths, which is small compared with the difference in ?14C in the added litter. The primary source of DOC within the mineral soil must therefore have been either the Oe/Oa horizon or the organic matter in the mineral soil. Over a 2-year time frame, leaching of DOC from recent litter did not have a major impact on the C stock in the mineral soil below 15 cm in this ecosystem.

Froeberg, Mats J [ORNL; Jardine, Philip M [ORNL; Hanson, Paul J [ORNL; Swanston, Christopher [ORNL; Todd Jr, Donald E [ORNL; Phillips, Jana Randolph [ORNL; Garten Jr, Charles T [ORNL

2007-01-01T23:59:59.000Z

5

Influence of Dissolved Organic Carbon and pH on Containment Sorption to Sediment  

DOE Green Energy (OSTI)

Low-Level Waste buried on the SRS contains cellulosic materials, Including wood, paper, and cardboard. Once buried, these materials are expected to degrade to form cellulose degradation products (CDP). Such materials are expected to influence radionuclide speciation in such a way that the radionuclides will sorb less to SRS Subsurface sediments and therefore would migrate more rapidly from the disposal site. The objective of this study was to quantify through laboratory work the influence of CDP and pH on radionuclide sorption to SRS subsurface sediments. The intent of this work was to create a Kd look-up table as a function of radionuclide, pH, and CDP concentration that could be used in future performance assessment calculations. Previous CDP-impacted Kd values were generated using two chemical analogues, UO2 2+ and Eu3+. This study collected data from a wider range of analogues to validate and/or refine this approach. An incomplete-randomized-block-statistical design was used in a laboratory sorption study involving 2 soil types (sandy and clay textured), 5 dissolved organic carbon concentrations (a measure of CDP), and 3 pH levels. Nonradioactive solutes were used as chemical analogues to the radionuclides of interest to the Low-Level Waste Performance Assessment: monovalent cations (K+ and Cs+), divalent cations (Ni2+ and Sr2+), trivalent cations (Ce3+ and Eu3+), tetravalent cations (Th4+ and Zr4+), and an anion (ReO4-). Analogues were matched to approximately 30 radionuclides based on similarities in periodicity and chemical properties. All CDP-impacted Kd values generated from this study were equal to or greater than those used in previous performance assessments. These larger Kd values may result in a greater Waste Acceptance Criteria (WAC), which in turn may permit greater amounts of Low-Level Waste to be safely disposed on site, saving the site the expense of shipping the waste off-site for disposal.

KAPLAN, DANIEL

2004-09-30T23:59:59.000Z

6

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 carbon (DOC) and other tracers are fractionated in relation to the initial water. Two separate “freeze-out” experiments were conducted to observe the effects of fractionation during ice formation. In experiment 1, marine and freshwater end members were mixed together in different ratios to create four different salinities. In experiment 2, a brackish water sample was collected. The initial unfrozen water, ice melt, and post-freeze brine water were tested for dissolved organic carbon, total nitrogen (TN), dissolved inorganic carbon (DIC), fluorescence and absorption (optics), water isotopes (?18O and ?D), and lignin phenols. Results showed a clear fractionation effect for all parameters, where the ice samples contained much less of the dissolved species than the enriched brine samples. This information is important to consider when trying using these parameters to determine the fate of carbon and the freshwater budget to the Arctic Ocean.

Smith, Stephanie 1990-

2012-05-01T23:59:59.000Z

7

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

8

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

9

Characterization of the dissolved organic matter in steam assisted gravity drainage boiler blow-down water.  

E-Print Network (OSTI)

??The presence of high concentrations of dissolved organic matter (DOM) and total dissolved solids (TDS) in the boiler blow-down water (BBD) causes severe equipment fouling… (more)

Guha Thakurta, Subhayan

2012-01-01T23:59:59.000Z

10

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

11

Aerosol organic carbon to black carbon ratios: Analysis of published...  

NLE Websites -- All DOE Office Websites (Extended Search)

Aerosol organic carbon to black carbon ratios: Analysis of published data and implications for climate forcing Title Aerosol organic carbon to black carbon ratios: Analysis of...

12

Rapid Field Measurement of Dissolved Inorganic Carbon Based on CO{sub 2} Analysis  

SciTech Connect

Dissolved inorganic carbon (DIC) is commonly measured in water and is an important parameter for understanding carbonate equilibrium, carbon cycling, and water-rock interaction. While accurate measurements can be made in the analytical laboratory, we have developed a rapid, portable technique that can be used to obtain accurate and precise data in the field as well.

VESPER, DJ, Edenborn, Harry

2012-01-01T23:59:59.000Z

13

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

E-Print Network (OSTI)

The vulnerability of the Arctic to climate change has been realized due to disproportionately large increases in surface air temperatures which are not uniformly distributed over the seasonal cycle. Effects of this temperature shift are widespread in the Arctic but likely include changes to the hydrological cycle and permafrost thaw, which have implications for the mobilization of organic carbon into rivers. The focus of this research was to describe the seasonal variability of the chemical composition of dissolved organic matter (DOM) in the six largest Arctic rivers (Yukon, Mackenzie, Ob, Yenisei, Lena and Kolyma) using optical properties (UV-Vis Absorbance and Fluorescence) and lignin phenol analysis. We also investigated differences between rivers and how watershed characteristics influence DOM composition. Dissolved organic carbon (DOC) concentrations followed the hydrograph with highest concentrations measured during peak river flow. The chemical composition of peak-flow DOM indicates a dominance of freshly leached material with elevated aromaticity, larger molecular weight, and elevated lignin yields relative to base-flow DOM. During peak flow, soils in the watershed are still frozen and snowmelt water follows a lateral flow path to the river channels. As the soils thaw, surface water penetrates deeper into the soil horizons leading to lower DOC concentrations and likely altered composition of DOM due to sorption and microbial degradation processes. The six rivers studied here shared a similar seasonal pattern and chemical composition. There were, however, large differences between rivers in terms of total carbon discharge reflecting the differences in watershed characteristics such as climate, catchment size, river discharge, soil types, and permafrost distribution. The large rivers (Lena, Yenisei), with a greater proportion of permafrost, exported the greatest amount of carbon. The Kolyma and Mackenzie exported the smallest amount of carbon annually, however, the discharge weighted mean DOC concentration was almost 2-fold higher in the Kolyma, again, indicating the importance of continuous permafrost. The quality and quantity of DOM mobilized into Arctic rivers appears to depend on the relative importance of surface run-off and extent of soil percolation. The relative importance of these is ultimately determined by watershed characteristics.

Rinehart, Amanda J.

2007-08-01T23:59:59.000Z

14

ARM - Measurement - Organic Carbon Concentration  

NLE Websites -- All DOE Office Websites (Extended Search)

govMeasurementsOrganic Carbon Concentration govMeasurementsOrganic Carbon Concentration ARM Data Discovery Browse Data Comments? We would love to hear from you! Send us a note below or call us at 1-888-ARM-DATA. Send Measurement : Organic Carbon Concentration The concentration of carbon bound in organic compounds. Categories Aerosols Instruments The above measurement is considered scientifically relevant for the following instruments. Refer to the datastream (netcdf) file headers of each instrument for a list of all available measurements, including those recorded for diagnostic or quality assurance purposes. ARM Instruments ACSM : Aerosol Chemical Speciation Monitor Field Campaign Instruments AEROSCARBON : Aerosol Carbon Analyzer AEROSMASSSPEC : Aerosol Mass Spectrometer Datastreams AOS : Aerosol Observing System Datastreams

15

Development of a dissolved carbon dioxide sensor with a HPTS-incorporated polymer membrane  

Science Conference Proceedings (OSTI)

In this study a dissolved carbon dioxide sensor is made by using the fluorescent dye, HPTS incorporated into a polymer matrix, polyHEMA-co-EGDA. The HPTS-incorporated polymer membrane soaking in sodium bicarbonate buffer solution is put into a well in ... Keywords: carbon dioxide, fermentation, fluorescence, polymer membrane, sensor

Ok-Jae Sohn; Jong Il Rhee

2008-11-01T23:59:59.000Z

16

Mechanisms controlling the production and transport of methane, carbon dioxide, and dissolved solutes within a boreal peatland  

SciTech Connect

Peatlands are one of the most important terrestrial reservoirs in the global cycle for carbon, and are a major source for atmospheric methane. However, little is known about the dynamics of these carbon reservoirs or their feedback mechanisms with the pool of atmospheric CO{sub 2} during the Holocene. Specifically, it is unknown whether large peat basins are sources, sinks, or steady-state reservoirs for the global carbon cycle. In particular, the production and transport of methane, carbon dioxide, and dissolved organic carbon form the deeper portions of these peatlands is unknown. Our DOE research program is to conduct an integrated ecologic and hydrogeochemical study of the Glacial Lake Agassiz peatlands (northern Minnesota) to better understand the carbon dynamics in globally significant peat basins. Specifically, our study will provide local and regional data on (1), rates of carbon accumulation and loss and fluxes of methane in the peat profiles; (2) the physical and botanical factors controlling the production of methane and carbon dioxide in the wetland; and (3) the role of hydrogeologic processes in controlling the fluxes of gases and solutes through the peat. We intend to use computer simulation models, calibrated to field data, to scale-up from local to regional estimates of methane and carbon dioxide within the basin. How gases and dissolved organic carbon escapes form peatlands in unknown. It has been suggested that the concentrations of methane produced in the upper peat are sufficient to produce diffusion gradients towards the surface. Alternatively, gas may move through the peat profile by groundwater advection.

Siegel, D.I.

1992-04-09T23:59:59.000Z

17

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

18

Dissolved organic matter and lake metabolism. Technical progress report, 1 April 1973--31 March 1974  

SciTech Connect

A detailed temporal and spatial carbon budget, essentially a functional detrital carbon budget, was evaluated for an oligotrophic lake system. Emphasis was placed on the fate and mechanisms regulating the qualitative and quantitative utilization and losses of organic carbon. (CH)

Wetzel, G.H.

1974-01-01T23:59:59.000Z

19

Reductive transformation of dioxins: An assessment of the contribution of dissolved organic matter to dechlorination reactions  

Science Conference Proceedings (OSTI)

The susceptibility of dioxins to dissolved organic carbon (DOC)-mediated dechlorination reactions was investigated using 1,2,3,4,6,7,9-heptachlorodibenzo-p-dioxin (HpCDD), Aldrich humic acid (AHA), and polymaleic acid (PMA) as model compounds. The dechlorination yields were on the order of 4--20% which, when normalized to phenolic acidity, was comparable to yields observed in the presence of the humic constituents catechol and resorcinol. Based on the ratio of dechlorination yields as a function of phenolic acidity and electron transfer capacity, differences in electron transfer efficiency to dioxins are likely combined effects of specific interactions with the functional groups and nonspecific hydrophobic interactions. Hexa- and pentaCDD homologues were dominant in all incubations, and diCDD constituted the final product of dechlorination. The rates of appearance of lesser chlorinated products were similar to those observed in sediment systems and followed thermodynamic considerations as they decreased with a decrease in level of chlorination. Generally, both absolute and phenolic acidity-normalized rate constants for AHA-mediated reactions were up to 2-fold higher than those effected by PMA. These results indicate that the electron shuttling capacity of sediment DOC may significantly affect the fate of dioxins, in part through dechlorination reactions.

Fu, Q.S.; Barkovskii, A.L.; Adriaens, P.

1999-11-01T23:59:59.000Z

20

Method for removing and decolorizing aqueous waste effluents containing dissolved or dispersed organic matter  

DOE Patents (OSTI)

A method is provided for treating organic waste material dissolved or dispersed in an aqueous effluent, which comprises contacting the effluent with an inert particulate carbonaceous sorbent at an oxygen pressure up to 2000 psi, irradiating the resultant mixture with high energy radiation until a decolorized liquid is produced, and then separating the decolorized liquid.

Case, F.N.; Ketchen, E.E.

1975-10-14T23:59:59.000Z

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

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

Science Conference Proceedings (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

22

Mechanisms controlling the production and transport of methane, carbon dioxide, and dissolved solutes within a boreal peatland. Progress report, January 15, 1991--July 14, 1992  

SciTech Connect

Peatlands are one of the most important terrestrial reservoirs in the global cycle for carbon, and are a major source for atmospheric methane. However, little is known about the dynamics of these carbon reservoirs or their feedback mechanisms with the pool of atmospheric CO{sub 2} during the Holocene. Specifically, it is unknown whether large peat basins are sources, sinks, or steady-state reservoirs for the global carbon cycle. In particular, the production and transport of methane, carbon dioxide, and dissolved organic carbon form the deeper portions of these peatlands is unknown. Our DOE research program is to conduct an integrated ecologic and hydrogeochemical study of the Glacial Lake Agassiz peatlands (northern Minnesota) to better understand the carbon dynamics in globally significant peat basins. Specifically, our study will provide local and regional data on (1), rates of carbon accumulation and loss and fluxes of methane in the peat profiles; (2) the physical and botanical factors controlling the production of methane and carbon dioxide in the wetland; and (3) the role of hydrogeologic processes in controlling the fluxes of gases and solutes through the peat. We intend to use computer simulation models, calibrated to field data, to scale-up from local to regional estimates of methane and carbon dioxide within the basin. How gases and dissolved organic carbon escapes form peatlands in unknown. It has been suggested that the concentrations of methane produced in the upper peat are sufficient to produce diffusion gradients towards the surface. Alternatively, gas may move through the peat profile by groundwater advection.

Siegel, D.I.

1992-04-09T23:59:59.000Z

23

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

Science Conference Proceedings (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.

2012-10-11T23:59:59.000Z

24

Worldwide organic soil carbon and nitrogen data  

Science Conference Proceedings (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

25

Soil organic carbon – A Western Australian perspective Soil organic carbon A Western Australian perspective  

E-Print Network (OSTI)

Sequestering carbon in soils is being investigated worldwide as a way to remove carbon dioxide from the atmosphere and provide land managers with extra income from the sale of carbon offsets or credits. In theory, the opportunity exists for farmers and other land managers to be paid via voluntary trades or carbon trading schemes to implement land management changes that sequester soil carbon, with additional benefits gained in improving the biological, chemical and physical health of their soils. The concept of increasing soil organic carbon is very attractive because it seemingly provides a ‘win-win’ situation in which farmers earn extra income for removing greenhouse gas emissions from the atmosphere while simultaneously lifting the productivity of arable soils. But how realistic is this concept and what opportunities and risks does it present to farmers? Soil organic carbon is part of the global carbon cycle The soil can either represent an enormous ‘source’ or ‘sink ’ of carbon – with more carbon contained in the soil than in the world’s vegetation and atmosphere combined. Soil organic carbon represents a critical component

Janet Paterson; Dr. Fran Hoyle; Department Of Agriculture

2011-01-01T23:59:59.000Z

26

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

27

Soil Organic Carbon Sequestration by Tillage and Crop Rotation...  

NLE Websites -- All DOE Office Websites (Extended Search)

Site Descriptions Soil Organic Carbon Sequestration by Tillage and Crop Rotation: A Global Data Analysis (Site Descriptions) West, T.O., and W.M. Post. 2002. Soil Organic Carbon...

28

Optimizing Carbon Nanotube Contacts for Use in Organic Photovoltaics: Preprint  

DOE Green Energy (OSTI)

This report describes research on optimizing carbon nanotube networks for use as transparent electrical contacts (TCs) in organic photovoltaics (OPV).

Barnes, T. M.; Blackburn, J. L.; Tenent, R. C.; Morfa, A.; Heben, M.; Coutts, T. J.

2008-05-01T23:59:59.000Z

29

Total organic carbon (TOC) and chemical oxygen demand (COD) - Monitoring of organic pollutants in wastewater.  

E-Print Network (OSTI)

?? Total organic carbon (TOC) and chemical oxygen demand (COD) are two methods used for measuring organic pollutants in wastewater. Both methods are widely used… (more)

Hodzic, Elvisa

2011-01-01T23:59:59.000Z

30

Challenges for improving estimates of soil organic carbon stored in  

NLE Websites -- All DOE Office Websites (Extended Search)

Challenges for improving estimates of soil organic carbon stored in Challenges for improving estimates of soil organic carbon stored in permafrost regions September 30, 2013 Tweet EmailPrint One of the greatest environmental challenges of the 21st century lies in predicting the impacts of anthropogenic activities on Earth's carbon cycle. Soil is a significant component of the carbon cycle, because it contains at least two-thirds of the world's terrestrial carbon and more than twice as much carbon as the atmosphere. Although soil organic carbon (SOC) stocks were built over millennial time scales, they are susceptible to a far more rapid release back to the atmosphere due to climatic and land use change. If environmental perturbations negatively impact the processes regulating the storage of SOC, significant amounts of this carbon could be decomposed

31

Estimation of the annual yield of organic carbon released from carbonates and shales by chemical weathering  

E-Print Network (OSTI)

Estimation of the annual yield of organic carbon released from carbonates and shales by chemical matter yield induced by chemical weathering of carbonates and shales, considering their global surface carbonate rocks and shales weathering in major world watersheds, published by numerous authors. The results

Paris-Sud XI, Université de

32

Soil Organic Carbon Sequestration in Reclaimed Minesoils  

NLE Websites -- All DOE Office Websites (Extended Search)

The SOC dynamics in soil macro and micro-aggregate fractions and its effect on long-term carbon (C) sequestration are discussed. Introduction Carbon (C) management in the next...

33

Contribution of organic carbon to wood smoke particulate matter absorption  

NLE Websites -- All DOE Office Websites (Extended Search)

Contribution of organic carbon to wood smoke particulate matter absorption Contribution of organic carbon to wood smoke particulate matter absorption of solar radiation Title Contribution of organic carbon to wood smoke particulate matter absorption of solar radiation Publication Type Journal Article Year of Publication 2012 Authors Kirchstetter, Thomas W., and Tracy L. Thatcher Journal Atmospheric Chemistry and Physics Volume 12 Pagination 6067-6072 Abstract A spectroscopic analysis of 115 wintertime partic- ulate matter samples collected in rural California shows that wood smoke absorbs solar radiation with a strong spectral se- lectivity. This is consistent with prior work that has demon- strated that organic carbon (OC), in addition to black car- bon (BC), appreciably absorbs solar radiation in the visible and ultraviolet spectral regions. We apportion light absorp-

34

Building and testing organized architectures of carbon nanotubes  

Science Conference Proceedings (OSTI)

This paper will focus on the directed assembly of multiwalled carbon nanotubes on various substrates into highly organized structures that include vertically and horizontally oriented arrays, ordered fibers and porous membranes. The concept of growing ...

R. Vajtai; Bingqing Wei; Yung Joon Jung; Anyuan Cao; S. K. Biswas; G. Ramanath; P. M. Ajayan

2003-12-01T23:59:59.000Z

35

Electrolytic dissolver  

DOE Patents (OSTI)

This patent related to an electrolytic dissolver wherein dissolution occurs by solution contact including a vessel of electrically insulative material, a fixed first electrode, a movable second electrode, means for insulating the electrodes from the material to be dissolved while permitting a free flow of electrolyte therebetween, means for passing a direct current between the electrodes and means for circulating electrolyte through the dissolver. (auth)

Wheelwright, E.J.; Fox, R.D.

1975-08-26T23:59:59.000Z

36

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

E-Print Network (OSTI)

power of radiocarbon in biogeochemical studies of the marinepower of radiocarbon in biogeochemical studies of the marine

De Jesus, Roman Paul

2008-01-01T23:59:59.000Z

37

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

E-Print Network (OSTI)

power of radiocarbon in biogeochemical studies of the marinepower of radiocarbon in biogeochemical studies of the marine

de Jesus, Roman P

2008-01-01T23:59:59.000Z

38

Chemistry of organic carbon in soil with relationship to the global carbon cycle  

SciTech Connect

Various ecosystem disturbances alter the balances between production of organic matter and its decomposition and therefore change the amount of carbon in soil. The most severe perturbation is conversion of natural vegetation to cultivated crops. Conversion of natural vegetation to cultivated crops results in a lowered input of slowly decomposing material which causes a reduction in overall carbon levels. Disruption of soil matrix structure by cultivation leads to lowered physical protection of organic matter resulting in an increased net mineralization rate of soil carbon. Climate change is another perturbation that affects the amount and composition of plant production, litter inputs, and decomposition regimes but does not affect soil structure directly. Nevertheless, large changes in soil carbon storage are probable with anticipated CO2 induced climate change, particularly in northern latitudes where anticipated climate change will be greatest (MacCracken and Luther 1985) and large amounts of soil organic matter are found. It is impossible, given the current state of knowledge of soil organic matter processes and transformations to develop detailed process models of soil carbon dynamics. Largely phenomenological models appear to be developing into predictive tools for understanding the role of soil organic matter in the global carbon cycle. In particular, these models will be useful in quantifying soil carbon changes due to human land-use and to anticipated global climate and vegetation changes. 47 refs., 7 figs., 2 tabs.

Post, W.M. III

1988-01-01T23:59:59.000Z

39

Sorption of organic carbon compounds to the fine fraction of surface and Subsurface Soils  

Science Conference Proceedings (OSTI)

Dissolved organic carbon (DOC) transported from the soil surface is stabilized in deeper soil profiles by physicochemical sorption processes. However, it is unclear how different forms of organic carbon (OC) compounds common in soil organic matter interact with soil minerals in the surface (A) and subsurface (B) horizons. We added four compounds (glucose, starch, cinnamic acid and stearic acid) to the silt- and clay-sized fraction (fine fraction) of A and B horizons of eight soils from varying climates (3 temperate, 3 tropical, 1 arctic and 1 sub-arctic). Equilibriumbatch experiments were conducted using 0 to 100 mg C L 1 of 14C-labeled compounds for 8 h. Sorption parameters (maximum sorption capacity, Qmax and binding coefficient, k) calculated by fitting sorption data to the Langmuir equation showed that Qmax of A and B horizons was very similar for all compounds. Both Qmax and k values were related to sorbate properties, with Qmax being lowest for glucose (20 500 mg kg 1), highest for stearic acid (20,000 200,000 mg kg 1), and intermediate for both cinnamic acid (200 4000 mg kg 1) and starch (400 6000 mg kg 1). Simple linear regression analysis revealed that physicochemical properties of the sorbents influenced the Qmax of cinnamic acid and stearic acid, but not glucose and starch. The sorbent properties did not show predictive ability for binding coefficient k. By using the fine fraction as sorbent, we found that the mineral fractions of A horizons are equally reactive as the B horizons irrespective of soil organic carbon content.

Jagadamma, Sindhu [ORNL; Mayes, Melanie [ORNL; Zinn, Yuri [Federal University of Lavras, Brazil; Gisladottir, Gudrun [University of Iceland; Ann, Russell [Iowa State University

2014-01-01T23:59:59.000Z

40

Shale-Derived Dissolved Organic Matter as a Substrate for Subsurface Methanogenic Communities in the Antrim Shale, Michigan Basin, USA.  

E-Print Network (OSTI)

??The microbial origin of methane produced from sedimentary basins is a subject of great interest, with implications for the global cycling of carbon as well… (more)

Huang, Roger

2008-01-01T23:59:59.000Z

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.


41

Soil Organic Carbon Change Monitored Over Large Areas  

DOE Green Energy (OSTI)

Soils account for the largest fraction of terrestrial carbon (C) and thus are critically important in determining global cycle dynamics. In North America, conversion of native prairies to agriculture over the past 150 years released 30- 50% of soil organic carbon (SOC) stores [Mann, 1986]. Improved agricultural practices could recover much of this SOC, storing it in biomass and soil and thereby sequestering billions of tons of atmospheric carbon dioxide (CO2). These practices involve increasing C inputs to soil (e.g., through crop rotation, higher biomass crops, and perennial crops) and decreasing losses (e.g., through reduced tillage intensity) [Janzen et al., 1998; Lal et al., 2003; Smith et al., 2007].

Brown, David J.; Hunt, E. Raymond; Izaurralde, Roberto C.; Paustian, Keith H.; Rice, Charles W.; Schumaker, Bonny L.; West, Tristram O.

2010-11-23T23:59:59.000Z

42

Carbon-catalyzed gasification of organic feedstocks in supercritical water  

Science Conference Proceedings (OSTI)

Spruce wood charcoal, macadamia shell charcoal, coal activated carbon, and coconut shell activated carbon catalyze the gasification of organic compounds in supercritical water. Feedstocks studied in this paper include glycerol, glucose, cellobiose, whole biomass feedstocks (depithed bagasse liquid extract and sewage sludge), and representative Department of Defense (DoD) wastes (methanol, methyl ethyl ketone, ethylene glycol, acetic acid, and phenol). The effects of temperature, pressure, reactant concentration, weight hourly space velocity, and the type of catalyst on the gasification of glucose are reported. Complete conversion of glucose (22% by weight in water) to a hydrogen-rich synthesis gas was realized at a weight hourly space velocity (WHSV) of 22.2 h{sup {minus}1} in supercritical water at 600 C, 34.5 MPa. Complete conversions of the whole biomass feeds were also achieved at the same temperature and pressure. The destruction efficiencies for the representative DoD wastes were also high. Deactivation of the carbon catalyst was observed after 4 h of operation without swirl in the entrance region of the reactor, but the carbon gasification efficiency remained near 100% for more than 6 h when a swirl generator was employed in the entrance of the reactor.

Xu, X.; Matsumura, Y.; Stenberg, J.; Antal, M.J. Jr. [Univ. of Hawaii, Honolulu, HI (United States). Hawaii Natural Energy Inst.

1996-08-01T23:59:59.000Z

43

Carbon Dioxide Separation with Novel Microporous Metal Organic Frameworks  

NLE Websites -- All DOE Office Websites (Extended Search)

David a. Lang David a. Lang Project Manager National Energy Technology Laboratory 626 Cochrans Mill Road P.O. Box 10940 Pittsburgh, PA 15236-0940 412-386-4881 david.lang@netl.doe.doe Richard Willis Principal Investigator UOP LLC 50 East Algonquin Road Des Plaines, IL 60016 847-391-3190 Richard.Willis@uop.com Carbon DioxiDe Separation with novel MiCroporouS Metal organiC FraMeworkS Background UOP LLC, in collaboration with Vanderbilt University and the University of Edinburgh, is working to develop novel microporous metal organic frameworks (MOFs) and an associated process for the removal of CO 2 from coal-fired power plant flue gas. This innovative project will exploit the latest discoveries in an extraordinary class of materials (MOFs) having extremely high adsorption capacities. MOFs have previously exhibited

44

Questions and Answers - Is carbon found in all organic and inorganic  

NLE Websites -- All DOE Office Websites (Extended Search)

atoms make up sugar? atoms make up sugar? Previous Question (What atoms make up sugar?) Questions and Answers Main Index Next Question (In the equation for methane, why is there more hydrogen than carbon?) In the equation for methane, why isthere more hydrogen than carbon? Is carbon found in all organic and inorganic matter? The answer is yes and no. Yes, carbon IS found in all organic matter, but NOT in inorganic matter. Although there are many definitions of "organic," in the scientific disciplines, the basic definition comes from chemistry. In chemistry, organic means chemical compounds with carbon in them. In a more general sense, organic refers to living things. And this is connected to the idea of organic chemistry being based on carbon compounds. Organic

45

Phototrophic Fe(II) Oxidation Promotes Organic Carbon Acquisition  

E-Print Network (OSTI)

Anoxygenic phototrophic Fe(II) oxidation is usually considered to be a lithoautotrophic metabolism that contributes to primary production in Fe-based ecosystems. In this study, we employed Rhodobacter capsulatus SB1003 as a model organism to test the hypothesis that phototrophic Fe(II) oxidation can be coupled to organic carbon acquisition. R. capsulatus SB1003 oxidized Fe(II) under anoxic conditions in a light-dependent manner, but it failed to grow lithoautotrophically on soluble Fe(II). When the strain was provided with Fe(II)-citrate, however, growth was observed that was dependent upon microbially catalyzed Fe(II) oxidation, resulting in the formation of Fe(III)-citrate. Subsequent photochemical breakdown of Fe(III)-citrate yielded acetoacetic acid that supported growth in the light but not the dark. The deletion of genes (RRC00247 and RRC00248) that encode homologs of atoA and atoD, required for acetoacetic acid utilization, severely impaired the ability of R. capsulatus SB1003 to grow on Fe(II)-citrate. The growth yield achieved by R. capsulatus SB1003 in the presence of citrate cannot be explained by lithoautotrophic growth on Fe(II) enabled by indirect effects of the ligand [such as altering the thermodynamics of Fe(II) oxidation or preventing cell encrustation]. Together, these results demonstrate that R. capsulatus SB1003 grows photoheterotrophically on Fe(II)-citrate. Nitrilotriacetic acid also supported light-dependent growth on Fe(II), suggesting that Fe(II) oxidation may be a general mechanism whereby some Fe(II)-oxidizing bacteria mine otherwise inaccessible organic carbon sources.

Rhodobacter Capsulatus Sb; Nicky C. Caiazza; Douglas P. Lies; Dianne K. Newman

2006-01-01T23:59:59.000Z

46

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 and by the fabrica- tion of an organic thin film transistor. An organic solar cell was fabricated from these com

Hong, Soon Hyung

47

Soil Organic Carbon Change Monitored Over Large Areas  

Science Conference Proceedings (OSTI)

Soils account for the largest fraction of terrestrial carbon (C); thus, they are critically important in determining global C cycle dynamics. In North America, conversion of native prairies to agricultural land use over 150 years ago released 30-50% of the soil organic carbon (SOC). Improved agricultural practices have the capacity to recover much of this SOC, storing it in biomass and soil and thereby removing billions of tons of atmospheric CO2. These practices involve increasing C inputs to soil (e.g., by crop rotations, increased use of higher biomass crops, perennial crops) and decreased losses (e.g., reduced tillage intensity) [Janzen et al., 1998; Lal et al., 2003; Smith et al., 2007]. Managing agricultural soils to increase SOC storage is a significant, immediately available, low-cost option for mitigating CO2 emissions, with a technical potential to offset as much as 800 Tg CO2/yr in the US (~13% of US CO2 emissions) [Lal et al., 2003] and 5000 Tg CO2/yr globally (~17% of global CO2 emissions) [Smith et al., 2007].

Brown, David J.; Hunt, E. Raymond; Izaurralde, Roberto C.; Paustian, Keith H.; Rice, Charles W.; West, Tristram O.; Schumaker, Bonny L.

2010-08-31T23:59:59.000Z

48

Changes in Soil Organic Carbon and Nitrogen as a Result of Cultivation  

NLE Websites -- All DOE Office Websites (Extended Search)

Research Program Abstract We assembed and analyzed a data base of soil organic carbon and nitrogen information from over 1100 profiles in order to explore factors...

49

Dissolver production tests  

SciTech Connect

In order to obtain data for the development and design of the Purex dissolvers and to demonstrate to Manufacturing and Technical personnel the feasibility of increasing the size of dissolver cuts at BiPO{sub 4} and Redox, a dissolver production test program in a BiPO{sub 4} dissolver is requested. These tests are expected to supplement the program already initiated on the 321 Bldg. dissolver, explaining dissolver behavior to the extent that existing dissolvers can be operated under more nearly optimum conditions and that new dissolvers can be designed with accuracy.

Tomlinson, R.E.

1952-08-05T23:59:59.000Z

50

Historical emissions of black and organic carbon aerosol from energy-related combustion, 18502000  

E-Print Network (OSTI)

Historical emissions of black and organic carbon aerosol from energy-related combustion, 1850) and primary organic carbon (OC) aerosols from fossil fuel and biofuel combustion between 1850 and 2000. We-related combustion, 1850­2000, Global Biogeochem. Cycles, 21, GB2018, doi:10.1029/2006GB002840. 1. Importance

Wisconsin at Madison, University of

51

Role of organic soils in the world carbon cycle: problem analysis and research needs  

SciTech Connect

In May 1979, The Institute of Ecology held a workshop to determine the role of organic soils in the global carbon cycle and to ascertain their past, present and future significance in world carbon flux. Wetlands ecologists and soil scientists who participated in the workshop examined such topics as Soils as Sources of Atmospheric CO/sub 2/, Organic Soils, Primary Production and Growth of Wetlands Ecosystems, and Management of Peatlands. The major finding of the workshop is that the organic soils are important in the overall carbon budget. Histosols and Gleysols, the major organic soil deposits of the world, normally sequester organic carbon fixed by plants. They may now be releasing enough carbon to account for nearly 10% of the annual rise in atmospheric content of CO/sub 2/.

Armentano, T.V. (ed.)

1980-02-01T23:59:59.000Z

52

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

SciTech Connect

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

53

Carbon Dioxide Separation with Novel Microporous Metal Organic Frameworks  

SciTech Connect

The goal of this program was to develop a low cost novel sorbent to remove carbon dioxide from flue gas and gasification streams in electric utilities. Porous materials named metal-organic frameworks (MOFs) were found to have good capacity and selectivity for the capture of carbon dioxide. Several materials from the initial set of reference MOFs showed extremely high CO{sub 2} adsorption capacities and very desirable linear isotherm shapes. Sample preparation occurred at a high level, with a new family of materials suitable for intellectual property protection prepared and characterized. Raman spectroscopy was shown to be useful for the facile characterization of MOF materials during adsorption and especially, desorption. Further, the development of a Raman spectroscopic-based method of determining binary adsorption isotherms was initiated. It was discovered that a stronger base functionality will need to be added to MOF linkers in order to enhance CO{sub 2} selectivity over other gases via a chemisorption mechanism. A concentrated effort was expended on being able to accurately predict CO{sub 2} selectivities and on the calculation of predicted MOF surface area values from first principles. A method of modeling hydrolysis on MOF materials that correlates with experimental data was developed and refined. Complimentary experimental data were recorded via utilization of a combinatorial chemistry heat treatment unit and high-throughput X-ray diffractometer. The three main Deliverables for the project, namely (a) a MOF for pre-combustion (e.g., IGCC) CO{sub 2} capture, (b) a MOF for post-combustion (flue gas) CO{sub 2} capture, and (c) an assessment of commercial potential for a MOF in the IGCC application, were completed. The key properties for MOFs to work in this application - high CO{sub 2} capacity, good adsorption/desorption rates, high adsorption selectivity for CO{sub 2} over other gases such as methane and nitrogen, high stability to contaminants, namely moisture, and easy regenerability, were all addressed during this program. As predicted at the start of the program, MOFs have high potential for CO{sub 2} capture in the IGCC and flue gas applications.

Richard Willis; Annabelle Benin; John Low; Ganesh Venimadhavan; Syed Faheem; David Lesch; Adam Matzger; Randy Snurr

2008-02-04T23:59:59.000Z

54

Feeding on ultraplankton and dissolved organic carbon in coral reefs: from the individual grazer to the community  

E-Print Network (OSTI)

A Review of the U.S. Department of Energy's Inertial Fusion Energy Program Rulon Linford,1) research carried out in contributing pro- grams. These programs include the heavy ion (HI) beam, the high of'' IFE research carried out in contributing programs. These programs include the HI beam, HAPL

Yahel, Gitai

55

Carbon Dioxide Separation with Novel Microporous Metal Organic Frameworks  

NLE Websites -- All DOE Office Websites (Extended Search)

Separation with Separation with Novel Microporous Metal Organic Frameworks Background UOP LLC, the University of Michigan, and Northwestern University are collaborating on a three-year program to develop novel microporous metal organic frameworks (MOFs) suitable for CO 2 capture and separation. MOFs are hybrid organic/inorganic structures in which the organic moiety is readily derivatized. This innovative program is using sophisticated molecular modeling to evaluate the structurally

56

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

57

Metal-Containing Organic and Carbon Aerogels for Hydrogen Storage  

SciTech Connect

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

58

The Impact of Marcellus Shale Total Organic Carbon on Productivity.  

E-Print Network (OSTI)

??In the Appalachian basin, the Devonian organic-rich shale interval, including the Marcellus Shale, is an important target for natural gas exploration. It has been utilized… (more)

Fakhouri, Eyad

2013-01-01T23:59:59.000Z

59

Aerosol organic carbon to black carbon ratios: Analysis of published data and implications for climate forcing  

E-Print Network (OSTI)

carbon particles in the Detroit urban area: Wintertimeparticulate concentrations in Detroit, Atmos. Environ. , 19,meteorological parameters in Detroit, Atmos. Environ. , 19,

Novakov, T.; Menon, S.; Kirchstetter, T.W.; Koch, D.; Hansen, J.E.

2005-01-01T23:59:59.000Z

60

Aerosol organic carbon to black carbon ratios: Analysis of published data and implications for climate forcing  

E-Print Network (OSTI)

Ryu (2004), Carbonaceous aerosol characteristics ofPM 2.5Allen (1990), Transported acid aerosols measured in southernconference international aerosol carbon round robin test

Novakov, T.; Menon, S.; Kirchstetter, T.W.; Koch, D.; Hansen, J.E.

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.


61

TethyanMediterranean organic carbon-rich sediments from Mesozoic black shales to sapropels  

E-Print Network (OSTI)

Tethyan­Mediterranean organic carbon-rich sediments from Mesozoic black shales to sapropels KAY@geowiss.uni-hamburg.de) Geological Institute, ETH Zurich, Zurich, Switzerland ABSTRACT The Jurassic to Holocene record of black shale sections or drill cores. The term `black shale' is used here broadly for sediments with elevated organic

Gilli, Adrian

62

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

63

Soil Organic Carbon Sequestration by Tillage and Crop Rotation: A Global  

NLE Websites -- All DOE Office Websites (Extended Search)

Tillage and Crop Rotation Tillage and Crop Rotation Soil Organic Carbon Sequestration by Tillage and Crop Rotation: A Global Data Analysis DOI: 10.3334/CDIAC/tcm.002 PDF file Full text Soil Science Society of America Journal 66:1930-1946 (2002) CSITE image Tristram O. West and Wilfred M. Post DOE Center for Carbon Sequestration in Terrestrial Ecosystems (CSiTE) Environmental Sciences Division Oak Ridge National Laboratory P.O. Box 2008 Oak Ridge, TN 37831-6290 U.S.A. Sponsor: U.S. Department of Energy's Office of Science, Biological and Environmental Research Program Abstract Global map Changes in agricultural management can potentially increase the accumulation rate of soil organic carbon (SOC), thereby sequestering CO2 from the atmosphere. This study was conducted to quantify potential soil

64

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

E-Print Network (OSTI)

Storage of Hydrogen, Methane, and Carbon Dioxide in Highly Porous Covalent Organic Frameworks projects aimed at using hydrogen as a clean fuel for automobiles and producing clean energy by designing achieve higher storage capacities for hydrogen, (1) (a) Leaf, D.; Verolmec, H. J. H.; Hunt, W. F., Jr. En

Yaghi, Omar M.

65

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

Science Conference Proceedings (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

66

Analysis of organic carbon and moisture in Hanford single-shell tank waste  

SciTech Connect

This report documents a revised analysis performed by Pacific Northwest Laboratory involving the organic carbon laboratory measurement data for Hanford single-shell tanks (SSTs) obtained from a review of the laboratory analytical data. This activity has as its objective to provide a best-estimate, including confidence levels, of total organic carbon (TOC) and moisture in each of the 149 SSTs at Hanford. The TOC and moisture information presented in this report is useful as part of the criteria to identify SSTs for additional measurements, or monitoring for the Organic Safety Program. In April 1994, an initial study of the organic carbon in Hanford single-shell tanks was completed at PNL. That study reflected the estimates of TOC based on tank characterizations datasets that were available at the time. Also in that study, estimation of dry basis TOC was based on generalized assumptions pertaining to the moisture of the tank wastes. The new information pertaining to tank moisture and TOC data that has become available from the current study influences the best estimates of TOC in each of the SSTs. This investigation of tank TOC and moisture has resulted in improved estimates based on waste phase: saltcake, sludge, or liquid. This report details the assumptions and methodologies used to develop the estimates of TOC and moisture in each of the 149 SSTs at Hanford.

Toth, J.J.; Heasler, P.G.; Lerchen, M.E.; Hill, J.G.; Whitney, P.D.

1995-05-01T23:59:59.000Z

67

The Minnesota Filter: A Tool for Capturing Stormwater Dissolved Phosphorus  

E-Print Network (OSTI)

://stormwater.safl.umn.edu/ Dissolved Pollutant Removal Processes · Vegetative processes: plant uptake and rhizospheric activity to nitrogen gas or petroleum hydrocarbons to carbon dioxide #12;http://stormwater.safl.umn.edu/ Phosphorus

Minnesota, University of

68

The mechanism of HF formation in LiPF6 based organic carbonate electrolytes  

NLE Websites -- All DOE Office Websites (Extended Search)

The mechanism of HF formation in LiPF6 based organic carbonate electrolytes The mechanism of HF formation in LiPF6 based organic carbonate electrolytes Title The mechanism of HF formation in LiPF6 based organic carbonate electrolytes Publication Type Journal Article Year of Publication 2012 Authors Lux, Simon F., Ivan T. Lucas, Elad Pollak, Stefano Passerini, Martin Winter, and Robert Kostecki Journal Electrochemistry Communications Volume 14 Start Page 47 Issue 1 Pagination 47-50 Date Published 01/2012 Keywords Hydrofluoric acid, LiPF6 degradation, Lithium ion batteries, spectroscopic ellipsometry Abstract Spectroscopic ellipsometry was used to study the time-dependent formation of HF upon the thermal degradation of LiPF6 at 50 °C in a lithium ion battery electrolyte containing ethylene carbonate and diethyl carbonate. The generated HF was monitored by following the etching rate of a 300 nm thick SiO2 layer, grown on both sides of a silicon wafer substrate, as a function of the immersion time in the electrolyte at 50 °C. It was found that the formation of HF starts after 70 h of exposure time and occurs following several different phases. The amount of generated HF was calculated using an empirical formula correlating the etching rate to the temperature. Combining the results of the HF formation with literature data, a simplified mechanism for the formation of the HF involving LiPF6 degradation, and a simplified catalytical reaction pathway of the formed HF and silicon dioxide are proposed to describe the kinetics of HF formation.

69

Bioavailable organic carbon in wetland soils across a broad climogeographic area  

E-Print Network (OSTI)

Soils from a broad climogeographic region of the U.S., ranging from Alaska to Louisiana and Texas, were obtained from the NRCS National Soils Laboratory in Lincoln, Nebraska. Soils were also collected in the summer of 1996 from upland and poorly drained areas in northern Alaska for comparison of biological properties and to determine the effects of drying on estimation of microbial biomass and activity. Air-dried soils were moistened and incubated 48 h, during which time CO? evolution was measured. Following the preincubation, microbial biomass was determined using a modification of the chloroform-fumigation-incubation method to accommodate limited sample quantity. Carbohydrates were determined using bicinchoninic acid reagent and total extractable carbon was determined by analysis of 0.5-M K?SO? extracts with a total carbon analyzer. The objectives of this study were to elucidate geographical trends and meaningful relationships between the bioavailable C parameters. Soil microbial biomass, determined by chloroform fumigation incubation, correlated best with organic C and basal respiration with subtraction of unfumigated controls. Extraction of C with hot water was a rapid, simple procedure that provided the best predictor of soil respiration. Potassium sulfate-extractable carbon was consistently lower than hot water extractable C. Soils from northern states tended to contain more organic carbon than soils in southern states, however, not necessarily more bioavailable C. Detecting geographical trends for bioavailable C proved more difficult due to numerous factors such as topographic position, surface vegetation, climate, and land use.

Baker, Andrew Dwight

2002-01-01T23:59:59.000Z

70

Reaction Mechanisms for the Limited Reversibility of Li-O2 Chemistry in Organic Carbonate Electrolytes  

SciTech Connect

The Li-O2 chemistry in nonaqueous carbonate electrolytes and the underneath reason of its limited reversibility was exhaustively investigated. The discharge products collected from the air cathode in a Li-O2 battery at different depth of discharge (DOD) were systematically analyzed with X-ray diffraction. It is revealed that, independent of the discharge depth, lithium alkylcarbonate (either lithium propylenedicarbonate - LPDC, or lithium ethylenedicarbonate - LEDC, with other related derivatives) and lithium carbonate (Li2CO3) are always the main products, obviously originated from the electrolyte solvents propylene carbonate (PC) and ethylene carbonate (EC). These lithium alkylcarbonates are obviously generated from the single-electron reductive decomposition of the corresponding carbonate solvents initiated by the attack of superoxide radical anions. On the other hand, neither lithium peroxide (Li2O2) nor lithium oxide (Li2O) is detected. More significantly, from in situ gas chromatography/mass spectroscopy it is found that Li2CO3 and Li2O cannot be oxidized even when charged up to 4.6 V vs. Li/Li+, while LPDC, LEDC and Li2O2 are readily able to, with CO2 and CO released with the re-oxidation of LPDC and LEDC. It is therefore concluded that the quasi-reversibility of Li-O2 chemistry observed hitherto in an organic carbonate-based electrolyte is actually reliant on the formation of lithium alkylcarbonates through the reductive decomposition of carbonate solvents during discharge process and the subsequent oxidation of these same alkylcarbonates during charge process. It is the poor oxidizability of these alkylcarbonate species that constitutes the obstruction to an ideal rechargeable Li-O2 battery.

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

2011-11-15T23:59:59.000Z

71

Paleoreconstruction of Particulate Organic Carbon Inputs to the High-Arctic Colville River Delta, Beaufort Sea, Alaska  

E-Print Network (OSTI)

High Arctic permafrosted soils represent a massive sink in the global carbon cycle, accounting for twice as much carbon as what is currently stored as carbon dioxide in the atmosphere. However, with current warming trends this sink is in danger of thawing and potentially releasing large amounts of carbon as both carbon dioxide and methane into the atmosphere. It is difficult to make predictions about the future of this sink without knowing how it has reacted to past temperature and climate changes. This dissertation summarizes the results of the first study to look at long term, fine scale organic carbon delivery by the high-Arctic Colville River into Simpson’s Lagoon in the near-shore Beaufort Sea. Modern delivery of organic carbon to the Lagoon was determined to come from a variety of sources through the use of a three end-member mixing model and sediment biomarker concentrations. These sources include the Colville River in the western area of the Lagoon near the river mouth, marine sources in areas of the Lagoon without protective barrier islands, and coastal erosional sources and the Mackenzie River in the eastern area of the Lagoon. Downcore organic carbon delivery was measured on two cores in the Lagoon, one taken near the mouth of the Colville River (spans about 1800 years of history) and one taken on the eastern end of the Lagoon (spans about 600 years of history). Bulk organic parameters and biomarkers were measured in both cores and analyzed with Principle Component Analysis to determine long-term trends in organic carbon delivery. It was shown that at various times in the past, highly degraded organic carbon inputs of what is likely soil and peat carbon were delivered to the Lagoon. At other times, inputs of fresher, non-degraded, terrestrially-derived organic carbon inputs of what are likely higher amounts of plant and vegetative material was delivered to the Lagoon. Inputs of degraded soil carbon were also shown to correspond to higher temperatures on the North Slope of Alaska, likely indicating that warmer temperatures lead to a thawing of permafrost and in turn organic carbon mobilization to the coastal Beaufort Sea.

Schreiner, Kathryn 1983-

2013-05-01T23:59:59.000Z

72

Electrochemical degradation characteristics of refractory organic pollutants in coking wastewater on multiwall carbon nanotube-modified electrode  

Science Conference Proceedings (OSTI)

The multiwall carbon nanotube-mollified electrode (MWCNT-ME) was fabricated and its electrocatalytic activity of refractory organic pollutants of coking wastewater was investigated. The surface morphology, absorption properties, and the electrochemical ...

Yan Wang; Shujing Sun; Guifu Ding; Hong Wang

2012-01-01T23:59:59.000Z

73

EVOLUTIONARY AND GEOLOGIC CONSEQUENCES OF ORGANIC CARBON FIXING IN THE PRIMITIVE ANOXIC OCEAN  

E-Print Network (OSTI)

photosynthesis primary carbon dioxide-fixing mechanism.trophic bacteria to fix carbon dioxide. These bacteria toas the primary energy fix carbon dioxide. The free source to

Berry, W.B.N.

2013-01-01T23:59:59.000Z

74

OBSERVATION Microbial Electrosynthesis: Feeding Microbes Electricity To Convert Carbon Dioxide and Water to Multicarbon Extracellular Organic Compounds  

E-Print Network (OSTI)

ABSTRACT The possibility of providing the acetogenic microorganism Sporomusa ovata with electrons delivered directly to the cells with a graphite electrode for the reduction of carbon dioxide to organic compounds was investigated. Biofilms of S. ovata growing on graphite cathode surfaces consumed electrons with the reduction of carbon dioxide to acetate and small amounts of 2-oxobutyrate. Electrons appearing in these products accounted for over 85 % of the electrons consumed. These results demonstrate that microbial production of multicarbon organic compounds from carbon dioxide and water with electricity as the energy source is feasible. IMPORTANCE Reducing carbon dioxide to multicarbon organic chemicals and fuels with electricity has been identified as an attractive strategy to convert solar energy that is harvested intermittently with photovoltaic technology and store it as covalent chemical bonds. The organic compounds produced can then be distributed via existing infrastructure. Nonbiological electrochemical reduction of carbon dioxide has proven problematic. The results presented here suggest that microbiological catalysts may be a robust alternative, and when coupled with photovoltaics, current-driven microbial carbon dioxide reduction represents a new form of photosynthesis that might convert solar energy to organic products more effectively than traditional biomass-based strategies.

Kelly P. Nevin; Trevor L. Woodard; Ashley E. Franks; Zarath M. Summers; Derek R. Lovley

2010-01-01T23:59:59.000Z

75

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

Science Conference Proceedings (OSTI)

Bioreduction-based strategies for remediating uranium (U)-contaminated sediments face the challenge of maintaining the reduced status of U for long times. Because groundwater influxes continuously bring in oxidizing terminal electron acceptors (O{sub 2}, NO{sub 3}{sup -}), it is necessary to continue supplying organic carbon (OC) to maintain the reducing environment after U bioreduction is achieved. We tested the influence of OC supply rates on mobility of previously microbial reduced uranium U(IV) in contaminated sediments. We found that high degrees of U mobilization occurred when OC supply rates were high, and when the sediment still contained abundant Fe(III). Although 900 days with low levels of OC supply minimized U mobilization, the sediment redox potential increased with time as did extractable U(VI) fractions. Molecular analyses of total microbial activity demonstrated a positive correlation with OC supply and analyses of Geobacteraceae activity (RT-qPCR of 16S rRNA) indicated continued activity even when the effluent Fe(II) became undetectable. These data support our earlier hypothesis on the mechanism responsible for re-oxidation of microbial reduced U(IV) under reducing conditions; that microbial respiration caused increased (bi)carbonate concentrations and formation of stable uranyl carbonate complexes, thereby shifted U(IV)/U(VI) equilibrium to more reducing potentials. The data also suggested that low OC concentrations could not sustain the reducing condition of the sediment for much longer time.

Wan, J.; Tokunaga, T.K.; Kim, Y.; Brodie, E.; Daly, R.; Hazen, T.C.; Firestone, M.K.

2008-05-15T23:59:59.000Z

76

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

E-Print Network (OSTI)

for measuring ecosystem carbon oxidation state and oxidativemean oxidation number of carbon (MOC) - A useful concept forJ.F. & Barsanti, K.C. The Carbon Number-Polarity Grid: A

Kroll, Jesse H.

2011-01-01T23:59:59.000Z

77

Comparison of sampling methods for semi-volatile organic carbonAssociated with PM2.5  

SciTech Connect

This study evaluates the influence of denuder sampling methods and filter collection media on the measurement of semi-volatile organic carbon (SVOC) associated with PM2.5. Two types of collection media, charcoal (activated carbon) and XAD, were used both in diffusion denuders and impregnated back-up filters in two different samplers, the VAPS and the PC-BOSS. The two organic diffusion denuders were XAD-coated glass annular denuders and charcoal-impregnated cellulose fiber filter(CIF) denuders. In addition, recently developed XAD-impregnated quartz filters were compared to CIF filters as back-up filter collection media. The two denuder types resulted in equivalent measurement of particulate organic carbon and particle mass. The major difference observed between the XAD and charcoal BOSS denuders is the higher efficiency of charcoal for collection of more volatile carbon. This more volatile carbon does not contribute substantially to the particle mass or SVOC measured as OC on quartz filters downstream of the denuders. This volatile carbon does result in high OC concentrations observed in charcoal filters placed behind quartz filters downstream of the XAD denuders and would result in overestimating the SVOC in that configuration.

Lewtas, Joellen; Booth, Derrick; Pang, Yanbo; Reimer, Steve; Eatough, Delbert J.; Gundel, Lara A.

2001-06-29T23:59:59.000Z

78

Method for dissolving plutonium dioxide  

DOE Patents (OSTI)

A method for dissolving plutonium dioxide comprises adding silver ions to a nitric acid-hydrofluoric acid solution to significantly speed up dissolution of difficultly soluble plutonium dioxide.

Tallent, Othar K. (Oak Ridge, TN)

1976-01-01T23:59:59.000Z

79

Identifying sources of dissolved organic carbon in agriculturally dominated rivers using radiocarbon age dating: Sacramento–San Joaquin River Basin, California  

E-Print Network (OSTI)

contribu- tion of water at the intake to the SWP on a dailySTHMFP—State Water Project SWP intake was the San Joaquinthan 50% of the water at the SWP intake; for the study

Sickman, James O.; DiGiorgio, Carol L.; Lee Davisson, M.; Lucero, Delores M.; Bergamaschi, Brian

2010-01-01T23:59:59.000Z

80

Influences of Organic Carbon Supply Rate on Uranium Bioreduction in Initially Oxidizing, Contaminated Sediment  

SciTech Connect

Remediation of uranium (U) contaminated sediments through in-situ stimulation of bioreduction to insoluble UO{sub 2} is a potential treatment strategy under active investigation. Previously, we found that newly reduced U(IV) can be reoxidized under reducing conditions sustained by a continuous supply of organic carbon (OC) because of residual reactive Fe(III) and enhanced U(VI) solubility through complexation with carbonate generated through OC oxidation. That finding motivated this investigation directed at identifying a range of OC supply rates that is optimal for establishing U bioreduction and immobilization in initially oxidizing sediments. The effects of OC supply rate, from 0 to 580 mmol OC (kg sediment){sup -1} year{sup -1}, and OC form (lactate and acetate) on U bioreduction were tested in flow-through columns containing U-contaminated sediments. An intermediate supply rate on the order of 150 mmol OC (kg sediment){sup -1} year{sup -1} was determined to be most effective at immobilizing U. At lower OC supply rates, U bioreduction was not achieved, and U(VI) solubility was enhanced by complexation with carbonate (from OC oxidation). At the highest OC supply rate, resulting highly carbonate-enriched solutions also supported elevated levels of U(VI), even though strongly reducing conditions were established. Lactate and acetate were found to have very similar geochemical impacts on effluent U concentrations (and other measured chemical species), when compared at equivalent OC supply rates. While the catalysts of U(VI) reduction to U(IV) are presumably bacteria, the composition of the bacterial community, the Fe reducing community, and the sulfate reducing community had no direct relationship with effluent U concentrations. The OC supply rate has competing effects of driving reduction of U(VI) to low solubility U(IV) solids, as well as causing formation of highly soluble U(VI)-carbonato complexes. These offsetting influences will require careful control of OC supply rates in order to optimize bioreduction-based U stabilization.

Tokunaga, Tetsu K.; Wan, Jiamin; Kim, Yongman; Daly, Rebecca A.; Brodie, Eoin L.; Hazen, Terry C.; Herman, Don; Firestone, Mary K.

2008-06-10T23:59:59.000Z

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

Method for dissolving plutonium dioxide  

DOE Patents (OSTI)

The fluoride-catalyzed, non-oxidative dissolution of plutonium dioxide in HNO.sub.3 is significantly enhanced in rate by oxidizing dissolved plutonium ions. It is believed that the oxidation of dissolved plutonium releases fluoride ions from a soluble plutonium-fluoride complex for further catalytic action.

Tallent, Othar K. (Oak Ridge, TN)

1978-01-01T23:59:59.000Z

82

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

83

Predicting Agricultural Management Influence on Long-Term Soil Organic Carbon Dynamics: Implications for Biofuel Production  

SciTech Connect

Long-term field experiments (LTE) are ideal for predicting the influence of agricultural management on soil organic carbon (SOC) dynamics and examining biofuel crop residue removal policy questions. Our objectives were (i) to simulate SOC dynamics in LTE soils under various climates, crop rotations, fertilizer or organic amendments, and crop residue managements using the CQESTR model and (ii) to predict the potential of no-tillage (NT) management to maintain SOC stocks while removing crop residue. Classical LTEs at Champaign, IL (1876), Columbia, MO (1888), Lethbridge, AB (1911), Breton, AB (1930), and Pendleton, OR (1931) were selected for their documented history of management practice and periodic soil organic matter (SOM) measurements. Management practices ranged from monoculture to 2- or 3-yr crop rotations, manure, no fertilizer or fertilizer additions, and crop residue returned, burned, or harvested. Measured and CQESTR predicted SOC stocks under diverse agronomic practices, mean annual temperature (2.1 19 C), precipitation (402 973 mm), and SOC (5.89 33.58 g SOC kg 1) at the LTE sites were significantly related (r 2 = 0.94, n = 186, P < 0.0001) with a slope not significantly different than 1. The simulation results indicated that the quantities of crop residue that can be sustainably harvested without jeopardizing SOC stocks were influenced by initial SOC stocks, crop rotation intensity, tillage practices, crop yield, and climate. Manure or a cover crop/intensified crop rotation under NT are options to mitigate loss of crop residue C, as using fertilizer alone is insufficient to overcome residue removal impact on SOC stocks

Gollany, H. T. [USDA ARS; Rickman, R. W. [USDA ARS; Albrecht, S. L. [USDA ARS; Liang, Y. [University of Arkansas; Kang, Shujiang [ORNL; Machado, S. [Oregon State University, Corvallis

2011-01-01T23:59:59.000Z

84

Distribution, Speciation, and Elemental Associations of Soil Organic Carbon under Varying Landscape Topographic Positions at the Molecular Scale  

E-Print Network (OSTI)

Distribution, Speciation, and Elemental Associations of Soil Organic Carbon under Varying Landscape spectra and maps were collected. Results: C Distribution and Associations with the Major Elements in Soil Clay Particles Fig.1. Relative elemental distribution maps (9µm�6µm) of clay fractions from the A

Sparks, Donald L.

85

Article Geography doi: 10.1007/s11434-012-5529-9 Preliminary estimation of the organic carbon pool in China’s wetlands  

E-Print Network (OSTI)

Accurate estimation of wetland carbon pools is a prerequisite for wetland resource conservation and implementation of carbon sink enhancement plans. The inventory approach is a realistic method for estimating the organic carbon pool in China’s wetlands at the national scale. An updated data and inventory approach were used to estimate the amount of organic carbon stored in China’s wetlands. Primary results are as follows: (1) the organic carbon pool of China’s wetlands is between 5.39 and 7.25 Pg, accounting for 1.3%–3.5 % of the global level; (2) the estimated values and percentages of the organic carbon contained in the soil, water and vegetation pools in China’s wetlands are 5.04–6.19 Pg and 85.4%–93.5%, 0.22–0.56 Pg and 4.1%–7.7%, 0.13–0.50 Pg and 2.4%–6.9%, respectively. The soil organic carbon pool of China’s wetlands is greater than our previous estimate of 3.67 Pg, but is lower than other previous estimates of 12.20 and 8–10 Pg. Based on the discussion and uncertainty analysis, some research areas worthy of future attention are presented. wetland carbon pool, inventory approach, remote sensing, soil carbon density, wetland vegetation Citation: Zheng Y M, Niu Z G, Gong P, et al. Preliminary estimation of the organic carbon pool in China’s wetlands. Chin Sci Bull,

Zheng Yaomin; Niu Zhenguo; Gong Peng; Dai Yongjiu; Shangguan Wei

2012-01-01T23:59:59.000Z

86

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

DOE Green Energy (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

87

Organic Carbon Cycling in East China Sea Shelf Sediments: Linkages with Hypoxia  

E-Print Network (OSTI)

The Changjiang River provides the main source of sediment and terrestrial derived organic carbon (OC) to the Changjiang large delta-front estuary (LDE) in the East China Sea (ECS). This study analyzed bulk OC, biomarkers including lignin and plant pigment, black carbon (BC) on ECS sediments sampled in winter 2009 and 2010 in order to study the OC cycling under the influence of natural and anthropogenic disturbance. Low-oxygen tolerant foraminiferal microfossils were analyzed in another two sediment cores to study the historical hypoxia events in the Changjiang LDE. Bulk carbon to nitrogen (C/N) ratio and stable isotope ?13C in the surface sediment samples indicated a mixture source of terrestrial, deltaic and marine derived OC. Refractory BC and reworked marine OC seemed to comprise most of the OC pool with older, less reactive signatures as deduced from ?14C, and BC analyses. Winter wind/wave energy and hydrodynamic sorting had a substantial winnowing effect on surface sediment OC redistribution. As a result, the highest lignin concentration shifted to the south during the 2010 cruise after the summer flood event. In addition, algal inputs from local deltaic lakes due to eutrophication and/or lateral transport likely caused the observed lack of benthic-pelagic coupling of pigment concentrations between the surface sediments and the water column after the summer flood in 2010. For the down-core sediment, the mass accumulation rate distribution followed the dispersal pathway of the ECS sediment. Terrestrial and marine derived OC showed significant spatial and temporal distribution. Lignin rich materials were better preserved in sediments closer to the coast while offshore sediments tended to be composed of lignin-poor, degraded OC, that were likely hydrodynamically sorted to a long distance during transport. Besides eutrophication, plant pigments indicated that marine-derived OC was mostly deposited in the sediment mixed layer with decay in the underlying sediment accumulation layer. The total OC standing stock since 1900 is approximately 1.62±1.15 kgC m^-2, about 1/10 of the total OC stock in all the middle and lower lakes in the Changjiang catchment. There has been an increase in the number of hypoxic bottom water events on the Changjiang LDE over the past 60 yrs indicated from the increases in low-oxygen tolerant foraminiferal microfossils due to excess deposition of OC and summer stratification.

Li, Xinxin

2013-05-01T23:59:59.000Z

88

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

SciTech Connect

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

89

Spatial and temporal distributions of particulate matter and particulate organic carbon, Northeast Gulf of Mexico  

E-Print Network (OSTI)

The distribution of particulate matter (PM) and particulate organic carbon (POC) was determined during the Northeast Gulf of Mexico Chemical Oceanography and Hydro-graphy program (NEGOM). The hydrography and physical forcing functions were examined to explain particulate matter distribution. PM and POC were determined for discrete samples, and PM was also compared with in situ beam attenuation measure-ments in order to make estimations of continuous particle concentration profiles. Measurements were made three times per year for three years, during 1997-1998, 1998-1999, and 1999-2000, but only the first two years' worth of results are reported here. PM distributions vary seasonally and interannually. General patterns tend to be fairly consistent spatially and temporally during fall and spring, but intensity changes accord-ing to season. Differences present at the surface appear to be due mainly to riverine input of nutrients and particles from the several major rivers that flow into the northeastern Gulf of Mexico. Wind-forced circulation appears to be a minor influence on surface particulate distribution. Secondary eddies can have an effect upon distribution, as seen with an anticyclonic feature over the upper slope during Summer 1998 which entrained less saline, high particulate river water offshore. A similar effect was noted during Summer 1999, but to a lesser degree. A shelf edge current associated with anticyclonic flow seems to be a mechanism responsible for the appearance of nepheloid layers on the outer shelf.

Bernal, Christina Estefana

2001-01-01T23:59:59.000Z

90

Organic analyses in water quality control programs - training manual  

Science Conference Proceedings (OSTI)

A lecture/laboratory manual dealing with the analysis of selected organic pollutants. Intended for use by those having little or no experience in the field, but having one year (or equivalent) of college organic chemistry, and having basic laboratory skills (volumetric glassware, titration assemblies, analytical and trip balances). Topics include dissolved oxygen, biochemical oxygen demand, ammonia, nitrates, nitrites, carbon analysis, chemical oxygen demand, surfactants, oil and grease phenolics, gas chromatography, and polychlorinated biphenyls.

Feldmann, C.

1980-11-01T23:59:59.000Z

91

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

Science Conference Proceedings (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

92

Carbon Dioxide Adsorption by Metal Organic Frameworks (Synthesis, Testing and Modeling).  

E-Print Network (OSTI)

??It is essential to capture carbon dioxide from flue gas because it is considered one of the main causes of global warming. Several materials and… (more)

Sabouni, Rana

2013-01-01T23:59:59.000Z

93

Historical emissions of black and organic carbon aerosol from energy-related combustion, 1850-2000 - article no. GB2018  

SciTech Connect

We present an emission inventory of primary black carbon (BC) and primary organic carbon (OC) aerosols from fossil fuel and biofuel combustion between 1850 and 2000. We reconstruct fossil fuel consumption and represent changes in technology on a national and sectoral basis. Our estimates rely on new estimates of biofuel consumption, and updated emission factors for old technologies. Emissions of black carbon increase almost linearly, totaling about 1000 Gg in 1850, 2200 Gg in 1900, 3000 Gg in 1950, and 4400 Gg in 2000. Primary organic carbon shows a similar pattern, with emissions of 4100 Gg, 5800 Gg, 6700 Gg, and 8700 Gg in 1850, 1900, 1950, and 2000, respectively. Biofuel is responsible for over half of BC emission until about 1890, and dominates energy-related primary OC emission throughout the entire period. Coal contributes the greatest fraction of BC emission between 1880 and 1975, and is overtaken by emissions from biofuel around 1975, and by diesel engines around 1990. Previous work suggests a rapid rise in BC emissions between 1950 and 2000. This work supports a more gradual increase between 1950 and 2000, similar to the increase between 1850 and 1925; implementation of clean technology is a primary reason.

Bond, T.C.; Bhardwaj, E.; Dong, R.; Jogani, R.; Jung, S.K.; Roden, C.; Streets, D.G.; Trautmann, N.M. [University of Illinois, Urbana, IL (USA). Dept. of Civil & Environmental Engineering

2007-05-15T23:59:59.000Z

94

DISSOLVED CONCENTRATION LIMITS OF RADIOACTIVE ELEMENTS  

Science Conference Proceedings (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

95

CALIFORNIUM ISOTOPES FROM BOMBARDMENT OF URANIUM WITH CARBON IONS  

E-Print Network (OSTI)

Isotopes from Bombardment of Uranium with Carbon Ions A.ISOTOPES FROM BOMBARDMENT OF URANIUM WITH CARBON IONS A.the irradiations, the uranium was dissolved in dilute

Ghiorso, A.; Thompson, S.G.; Street, K. Jr.; Seaborg, G.T.

2008-01-01T23:59:59.000Z

96

The Dissolution of Desicooler Residues in H-Canyon Dissolvers  

Science Conference Proceedings (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

97

Modeling the heat and mass transfers in temperature-swing adsorption of volatile organic compounds onto activated carbons  

Science Conference Proceedings (OSTI)

A theoretical model was built to simulate the adsorption of volatile organic compounds (VOCs) onto activated carbons in a fixed bed. This model was validated on a set of experimental data obtained for the adsorption of acetone, ethyl formate, and dichloromethane onto five commercial activated carbons. The influence of operating conditions was modeled with various VOC contents at the inlet of the adsorber and superficial velocities of the gas-phase from 0.14 to 0.28 m.s{sup -1}. Breakthrough times and maximum temperature rises were computed with a coefficient of determination of 0.988 and 0.901, respectively. The simulation was then extended to the adsorption of mixtures of VOCs. From the comparison of simulation and experimental results, the advantage of accounting for dispersions of heat and mass is shown and the importance in taking into account the temperature effect on the equilibrium data is demonstrated. 29 refs., 6 figs., 1 tab.

Sylvain Giraudet; Pascaline Pre; Pierre Le Cloirec [Ecole des Mines de Nantes, Nantes (France)

2009-02-15T23:59:59.000Z

98

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

Science Conference Proceedings (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

99

Bead and Process for Removing Dissolved Metal Contaminants  

DOE Patents (OSTI)

A bead is provided which comprises or consists essentially of activated carbon immobilized by crosslinked poly (carboxylic acid) binder, sodium silicate binder, or polyamine binder. The bead is effective to remove metal and other ionic contaminants from dilute aqueous solutions. A method of making metal-ion sorbing beads is provided, comprising combining activated carbon, and binder solution (preferably in a pin mixer where it is whipped), forming wet beads, and heating and drying the beads. The binder solution is preferably poly(acrylic acid) and glycerol dissolved in water and the wet beads formed from such binder solution are preferably heated and crosslinked in a convection oven.

Summers, Bobby L., Jr.; Bennett, Karen L.; Foster, Scott A.

2005-01-18T23:59:59.000Z

100

DISSOLVED CONCENTRATION LIMITS OF RADIOACTIVE ELEMENTS  

Science Conference Proceedings (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.


101

Processes Affecting Agricultural Drainwater Quality and Organic Carbon Loads in California's Sacramento-San Joaquin Delta  

E-Print Network (OSTI)

Wang, and S. Rojstaczer. 1998. Subsidence of organic soils,Prokopovich, N.P. 1985. Subsidence of peat in California andDeverel, S.J. 1998. Subsidence mitigation in the Sacramento-

Deverel, Steven J; Leighton, David A; Finlay, Mark R

2007-01-01T23:59:59.000Z

102

Impact of Post-Synthesis Modification of Nanoporous Organic Frameworks on Selective Carbon Dioxide Capture.  

E-Print Network (OSTI)

??Porous organic polymers containing nitrogen-rich building units are among the most promising materials for selective CO2 capture and separation applications that impact the environment and… (more)

?slamo?lu, Timur

2013-01-01T23:59:59.000Z

103

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

E-Print Network (OSTI)

Sun, Y. et al. Size-resolved aerosol chemistry on Whistlerwith a high-resolution aerosol mass spectrometer duringBasis Set: 1. Organic-Aerosol Mixing Thermodynamics. Atmos.

Kroll, Jesse H.

2011-01-01T23:59:59.000Z

104

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

105

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

106

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

DOE Green Energy (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

107

Wormhole formation in dissolving fractures  

E-Print Network (OSTI)

We investigate the dissolution of artificial fractures with three-dimensional, pore-scale numerical simulations. The fluid velocity in the fracture space was determined from a lattice-Boltzmann method, and a stochastic solver was used for the transport of dissolved species. Numerical simulations were used to study conditions under which long conduits (wormholes) form in an initially rough but spatially homogeneous fracture. The effects of flow rate, mineral dissolution rate and geometrical properties of the fracture were investigated, and the optimal conditions for wormhole formation determined.

Szymczak, P

2009-01-01T23:59:59.000Z

108

PROCESS OF DISSOLVING ZIRCONIUM ALLOYS  

DOE Patents (OSTI)

A process is described for dissolving binary zirconium-uranium alloys where the uranium content is about 2%. In prior dissolution procedures for these alloys, an oxidizing agent was added to prevent the precipitation of uranium tetrafluoride. In the present method complete dissolution is accomplished without the use of the oxidizing agent by using only the stoichiometric amount or slight excess of HF required by the zirconium. The concentration of the acid may range from 2M to 10M and the dissolution is advatageously carried out at a temperature of 80 deg C.

Shor, R.S.; Vogler, S.

1958-01-21T23:59:59.000Z

109

A committee machine with intelligent systems for estimation of total organic carbon content from petrophysical data: An example from Kangan and Dalan reservoirs in South Pars Gas Field, Iran  

Science Conference Proceedings (OSTI)

Total organic carbon (TOC) content present in reservoir rocks is one of the important parameters, which could be used for evaluation of residual production potential and geochemical characterization of hydrocarbon-bearing units. In general, organic-rich ... Keywords: Committee machine, Fuzzy logic, Genetic algorithm, Neural network, Neuro-fuzzy, Petrophysical data, South Pars Gas Field, Total organic carbon

Ali Kadkhodaie-Ilkhchi; Hossain Rahimpour-Bonab; Mohammadreza Rezaee

2009-03-01T23:59:59.000Z

110

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

SciTech Connect

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

111

Organization  

NLE Websites -- All DOE Office Websites (Extended Search)

Organization Print Organization Print 2012-12 org chart A complete ALS organization chart (June 2013) is available in PDF. Appointed and elected members of advisory panels provide guidance to Berkeley Lab and ALS management in developing the ALS scientific and user programs. ALS Staff Photo staff photo thumb Click on the image to see a recent photo of ALS staff in front of the dome. The photo was taken on May 14, 2013. ALS Management and Advisory Team Steve Kevan, Deputy Division Director, Science Michael J. Banda, Deputy Division Director, Operations Robert W. Schoenlein, Senior Staff Scientist, Next Generation Light Source Initiative Janos Kirz, Scientific Advisor Paul Adams, Division Deputy for Biosciences ALS Scientific, Technical, and User Support Groups Accelerator Physics

112

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

SciTech Connect

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

113

Nanostructured Electrodes For Organic Bulk Heterojunction Solar Cells: Model Study Using Carbon Nanotube Dispersed Polythiophene-fullerene Blend Devices  

Science Conference Proceedings (OSTI)

We test the feasibility of using nanostructured electrodes in organic bulk heterojunction solar cells to improve their photovoltaic performance by enhancing their charge collection efficiency and thereby increasing the optimal active blend layer thickness. As a model system, small concentrations of single wall carbon nanotubes are added to blends of poly(3-hexylthiophene): [6,6]-phenyl-C{sub 61}-butyric acid methyl ester in order to create networks of efficient hole conduction pathways in the device active layer without affecting the light absorption. The nanotube addition leads to a 22% increase in the optimal blend layer thickness from 90 nm to 110 nm, enhancing the short circuit current density and photovoltaic device efficiency by as much as {approx}10%. The associated incident-photon-to-current conversion efficiency for the given thickness also increases by {approx}10% uniformly across the device optical absorption spectrum, corroborating the enhanced charge carrier collection by nanostructured electrodes.

Nam, C.Y.; Wu, Q.; Su, D.; Chiu, C.-y; Tremblay, N.J.; Nuckolls, C,; Black, C.T.

2011-09-19T23:59:59.000Z

114

METHOD OF DISSOLVING REFRACTORY ALLOYS  

DOE Patents (OSTI)

This patent relates to the dissolution of alloys of uranium with zirconium, thorium, molybdenum, or niobium. The alloy is contacted with an anhydrous solution of mercuric chloride in a low-molecular-weight monohydric alcohol to produce a mercury-containing alcohol slurry. The slurry is then converted to an aqueous system by adding water and driving off the alcohol. The resulting aqueous slurry is electrolyzed in the presence of a mercury cathode to remove the mercury and produce a uranium-bearing aqueous solution. This process is useful for dissolving irradiated nuclear reactor fuels for radiochemical reprocessing by solvent extraction. In addition, zirconium-alloy cladding is selectively removed from uranium dioxide fuel compacts by this means. (AEC)

Helton, D.M.; Savolainen, J.K.

1963-04-23T23:59:59.000Z

115

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

116

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

SciTech Connect

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

117

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

Science Conference Proceedings (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

118

Carbon Dioxide Removal from Flue Gas Using Microporous Metal Organic Frameworks  

SciTech Connect

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

119

Constraining oceanic dust deposition using surface ocean dissolved Al  

E-Print Network (OSTI)

Iron, manganese and lead at Hawaii Ocean Time-series stationof beryllium to the oceans, Earth Planet. Sci. Lett. , 114,organic carbon fluxes in the ocean based on the quantitative

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

2008-01-01T23:59:59.000Z

120

Dissolving uranium oxide--aluminum fuel  

SciTech Connect

The dissolution of aluminum-clad uranium oxide-aluminum fuel was studied to provide basic data for dissolving this type of enriched uranium fuel at the Savannah River Plant. The studies also included the dissolution of a similar material prepared from scrap uranium oxides that were to be recycled through the solvent extraction process. The dissolving behavior of uranium oxide-aluminum core material is similar to that of U-Al alloy. Dissolving rates are rapid in HNO/sub 3/-Hg(NO/sub 3/)/sub 2/ solutions. Irradiation reduce s the dissolving rate and increases mechanical strength. A dissolution model for use in nuclear safety analyses is developed, . based on the observed dissolving characteristics. (auth)

Perkins, W.C.

1973-11-01T23:59:59.000Z

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.


121

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

SciTech Connect

Two gas storage fields were studied for this project. Overisel field, operated by Consumer's Energy, is located near the town of Holland, Michigan. Huntsman Storage Unit, operated by Kinder Morgan, is located in Cheyenne County, Nebraska near the town of Sidney. Wells in both fields experienced declining performance over several years of their annual injection/production cycle. In both fields, the presence of hydrocarbons, organic materials or production chemicals was suspected as the cause of progressive formation damage leading to the performance decline. Core specimens and several material samples were collected from these 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

2004-06-30T23:59:59.000Z

122

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

123

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

124

Three Letters to an Architect Dissolving  

E-Print Network (OSTI)

Three Letters to an Architect Dissolving Douglas Dardendeceive yourself. To be an architect is to lay d o w n y o uheavy earth. Give up, architect: n o m a n , and less the

Darden, Douglas

1987-01-01T23:59:59.000Z

125

Dissolved organic matters impact on colour reconstruction in underwater images  

Science Conference Proceedings (OSTI)

The natural properties of water column usually affect underwater imagery by suppressing high-energy light. In application such as color correction of underwater images estimation of water column parameters is crucial. Diffuse attenuation coefficients ...

J. Ĺhlén; D. Sundgren; T. Lindell; E. Bengtsson

2005-06-01T23:59:59.000Z

126

Process for coal liquefaction in staged dissolvers  

SciTech Connect

There is described an improved liquefaction process by which coal is converted to a low ash and low sulfur carbonaceous material that can be used as a fuel in an environmentally acceptable manner without costly gas scrubbing equipment. In the process, coal is slurried with a pasting oil, passed through a preheater and at least two dissolvers in series in the presence of hydrogen-rich gases at elevated temperatures and pressures. Solids, including mineral ash and unconverted coal macerals, are separated from the condensed reactor effluent. In accordance with the improved process, the first dissolver is operated at a higher temperature than the second dissolver. This temperature sequence produces improved product selectivity and permits the incorporation of sufficient hydrogen in the solvent for adequate recycle operations.

Roberts, George W. (Emmaus, PA); Givens, Edwin N. (Bethlehem, PA); Skinner, Ronald W. (Allentown, PA)

1983-01-01T23:59:59.000Z

127

Carbon Sequestration - Public Meeting  

NLE Websites -- All DOE Office Websites (Extended Search)

Public Meeting Programmatic Environmental Impact Statement Public Meeting May 18, 2004 National Energy Technology Laboratory Office of Fossil Energy Scott Klara Carbon Sequestration Technology Manager Carbon Sequestration Program Overview * What is Carbon Sequestration * The Fossil Energy Situation * Greenhouse Gas Implications * Pathways to Greenhouse Gas Stabilization * Sequestration Program Overview * Program Requirements & Structure * Regional Partnerships * FutureGen * Sources of Information What is Carbon Sequestration? Capture can occur: * at the point of emission * when absorbed from air Storage locations include: * underground reservoirs * dissolved in deep oceans * converted to solid materials * trees, grasses, soils, or algae Capture and storage of CO 2 and other Greenhouse Gases that

128

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

SciTech Connect

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

129

In-situ photocatalytic remediation of organic contaminants in groundwater  

E-Print Network (OSTI)

Dissolved Organic Carbon DWI Drinking Water Inspectorate E Energy level of photon in electron volt EDX Energy-Dispersive X-ray spectroscopy ecb- Conduction band electron Eg Energy bandgap EIA Energy Information Administration etr- Electron trapped... in the conduction band eV Electron volt Fe Iron or ferrum Fe2+ Ferrous ion Fe3+ Ferric ion g Gram(s) [M] xxxiv GC Gas chromatograph GC-FID Gas chromatograph with flame ionisation detector h Hour(s) [T] H Height [L] H Henry’s law constant [M L-3 (M-1 L-3...

Lim, Leonard Lik Pueh

2010-07-06T23:59:59.000Z

130

Acetylenic carbon allotrope  

DOE Patents (OSTI)

A fourth allotrope of carbon, an acetylenic carbon allotrope, is described. The acetylenic carbon allotropes of the present invention are more soluble than the other known carbon allotropes in many common organic solvents and possesses other desirable characteristics, e.g. high electron density, ability to burn cleanly, and electrical conductive properties. Many uses for this fourth allotrope are described herein.

Lagow, Richard J. (6204 Shadow Mountain Dr., Austin, TX 78731)

1998-01-01T23:59:59.000Z

131

Acetylenic carbon allotrope  

DOE Patents (OSTI)

A fourth allotrope of carbon, an acetylenic carbon allotrope, is described. The acetylenic carbon allotropes of the present invention are more soluble than the other known carbon allotropes in many common organic solvents and possesses other desirable characteristics, e.g. high electron density, ability to burn cleanly, and electrical conductive properties. Many uses for this fourth allotrope are described herein. 17 figs.

Lagow, R.J.

1998-02-10T23:59:59.000Z

132

Acetylenic carbon allotrope  

DOE Patents (OSTI)

A fourth allotrope of carbon, an acetylenic carbon allotrope, is described. The acetylenic carbon allotropes of the present invention are more soluble than the other known carbon allotropes in many common organic solvents and possesses other desirable characteristics, e.g. high electron density, ability to burn cleanly, and electrical conductive properties. Many uses for this fourth allotrope are described herein.

Lagow, Richard J. (6204 Shadow Mountain Dr., Austin, TX 78731)

1999-01-01T23:59:59.000Z

133

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

134

Efficient Organic Excitonic Solar Cells with Carbon Nanotubes Replacing In2O3:Sn as the Transparent Electrode (Presentation)  

DOE Green Energy (OSTI)

The conclusions of this report are that: (1) organic solar cells with efficiencies of up to 1.43% conversion efficiency that use no ITO and no PEDOT:PSS, are demonstrated; (2) a cell without ITO, but with PEDOT:PSS gave 2.6% conversion efficiency; (3) due to porous nature of SWCNT substrates, optimization of the active layer is essential; and (4) SWCNT electrodes bring one step closer the goal of a fully printable, organic solar cell.

van de Lagemaat, J.; Barnes, T.; Rumbles, G.; Shaheen, S.; Coutts, T. J.; Weeks, C.; Glatkowski, P.; Levitsky, I.; Peltola, J.

2006-05-01T23:59:59.000Z

135

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

SciTech Connect

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

136

HB-Line Dissolver Dilution Flows and Dissolution Capability with Dissolver Charge Chute Cover Off  

DOE Green Energy (OSTI)

A flow test was performed in Scrap Recovery of HB-Line to document the flow available for hydrogen dilution in the dissolvers when the charge chute covers are removed. Air flow through the dissolver charge chutes, with the covers off, was measured. A conservative estimate of experimental uncertainty was subtracted from the results. After subtraction, the test showed that there is 20 cubic feet per minute (cfm) air flow through the dissolvers during dissolution with a glovebox exhaust fan operating, even with the scrubber not operating. This test also showed there is 6.6 cfm air flow through the dissolvers, after subtraction of experimental uncertainty if the scrubber and the glovebox exhaust fans are not operating. Three H-Canyon exhaust fans provide sufficient motive force to give this 6.6 cfm flow. Material charged to the dissolver will be limited to chemical hydrogen generation rates that will be greater than or equal to 25 percent of the Lower Flammability Limit (LFL) during normal operations. The H-Canyon fans will maintain hydrogen below LFL if electrical power is lost. No modifications are needed in HB-Line Scrap Recovery to ensure hydrogen is maintained less that LFL if the scrubber and glovebox exhaust fans are not operating.

Hallman, D.F.

2003-01-15T23:59:59.000Z

137

CARBON TECHNOLOGY: I: Petroleum Coke  

Science Conference Proceedings (OSTI)

CARBON TECHNOLOGY: Session I: Petroleum Coke. Sponsored by: LMD Aluminum Committee Program Organizer: Jean-Claude Thomas , Aluminium ...

138

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

Science Conference Proceedings (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

139

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

SciTech Connect

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

140

System to Continuously Produce Carbon Fiber via Microwave-Assisted ...  

Biomass and Biofuels; Building ... Carbon and graphite fibers are conventionally produced through the controlled pyrolysis of fibrous organic carbon precursors ...

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

One-step production of lactate from cellulose as the sole carbon source without any other organic nutrient by recombinant cellulolytic Bacillus subtilis  

NLE Websites -- All DOE Office Websites (Extended Search)

step step production of lactate from cellulose as the sole carbon source without any other organic nutrient by recombinant cellulolytic Bacillus subtilis Xiao-Zhou Zhang a , Noppadon Sathitsuksanoh a,b , Zhiguang Zhu a , Y.-H. Percival Zhang a,b,c,n a Department of Biological Systems Engineering, Virginia Tech, Blacksburg, VA 24061, USA b Institute for Critical Technology and Applied Science, Virginia Tech, Blacksburg, VA 24061, USA c BioEnergy Science Center, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA a r t i c l e i n f o Article history: Received 28 December 2010 Received in revised form 9 April 2011 Accepted 25 April 2011 Keywords: Bacillus subtilis Cellulase engineering Consolidated bioprocessing Endoglucanase Lactate Metabolic engineering Directed evolution a b s t r a c t Although intensive efforts have been made to create recombinant cellulolytic microorganisms,

142

Alcohol fuel use: Implications for atmospheric levels of aldehydes, organic nitrates, pans, and peroxides: Separating sources using carbon isotopes  

DOE Green Energy (OSTI)

We have developed DiNitroPhenylHydrazone (DNPH) derivatization--high performance liquid chromatographic methods for measuring aldehydes in ambient samples with detection limits of approximately 1ppbV. These methods can be used for air or precipitation studies, and have been used for indoor measurements at much higher levels using shorter integration times. We are using gas chromatographs with electron capture detection (GCECD) to measure ambient levels of peroxyacyl nitrates and organic nitrates. Diffusion tubes with synthetically produced organic nitrates in n-tridecane solution are used to calibrate these systems. These compounds are important means of transporting NO/sub x/ over large scales due to their reduced tropospheric reactivity, low water solubilities, photolytic, and thermal stability. Their chemistries are coupled to aldehyde chemistry and are important greenhouse gases as well as phytotoxins. We have completed preliminary studies in Rio de Janeiro examining the atmospheric chemistry consequences of ethanol fuel usage. The urban air mass has been effected by the direct uncontrolled usage of ethanolgasoline and ethanoldiesel mixtures. We are exploring the use of luminol chemiluminescent detection of peroxides using gas chromatography to separate the various organic and inorganic peroxides. These compounds are coupled to the aldehyde chemistry, particularly in remote chemistries down-wind of urban sources. 13 refs.

Gaffney, J.S.; Tanner, R.L.

1988-01-01T23:59:59.000Z

143

Tuning the Gate Opening Pressure of Metal Organic Frameworks (MOFs) for the Selective Separation of Hydro-carbons  

E-Print Network (OSTI)

Separation of hydrocarbons is one of the most energy demanding processes. The need to develop materials for the selective adsorption of hydrocarbons, under reasonable conditions, is therefore of paramount importance. This work unveils unexpected hydrocarbon selectivity in a flexible Metal Organic Framework (MOF), based on differences in their gate opening pressure. We show selectivity dependence on both chain length and specific framework-gas interaction. Combining Raman spectroscopy and theoretical van der Waals Density Functional (vdW-DF) calculations, the separation mechanisms governing this unexpected gate opening behavior are revealed.

Nijem, Nour; Canepa, Pieremanuele; Marti, Anne; Balkus,, Kenneth J; Thonhauser, T; Li, Jing; Chabal, Yves J; 10.1021/ja305754f

2012-01-01T23:59:59.000Z

144

Method for dissolving delta-phase plutonium  

DOE Patents (OSTI)

A process for dissolving plutonium, and in particular, delta-phase plutonium. The process includes heating a mixture of nitric acid, hydroxylammonium nitrate and potassium fluoride (HAN) to a temperature between 40 and 70 C, then immersing the metal in the mixture. Preferably, the nitric acid has a concentration of not ore than 2M, the HAN approximately 0.66M, and the potassium fluoride 1M. Additionally, a small amount of sulfamic acid, such as 0.1M can be added to assure stability of the HAN in the presence of nitric acid. The oxide layer that forms on plutonium metal may be removed with a non-oxidizing acid as a pre-treatment step.

Karraker, D.G.

1992-12-31T23:59:59.000Z

145

METHOD FOR DISSOLVING LANTHANUM FLUORIDE CARRIER FOR PLUTONIUM  

DOE Patents (OSTI)

A method is described for dissolving lanthanum fluoride precipitates which is applicable to lanthanum fluoride carrier precipitation processes for recovery of plutonium values from aqueous solutions. The lanthanum fluoride precipitate is contacted with an aqueous acidic solution containing dissolved zirconium in the tetravalent oxidation state. The presence of the zirconium increases the lanthanum fluoride dissolved and makes any tetravalent plutonium present more readily oxidizable to the hexavalent state. (AEC)

Koshland, D.E. Jr.; Willard, J.E.

1961-08-01T23:59:59.000Z

146

Method for dissolving plutonium oxide with HI and separating plutonium  

DOE Patents (OSTI)

PuO.sub.2 -containing solids, particularly residues from incomplete HNO.sub.3 dissolution of irradiated nuclear fuels, are dissolved in aqueous HI. The resulting solution is evaporated to dryness and the solids are dissolved in HNO.sub.3 for further chemical reprocessing. Alternatively, the HI solution containing dissolved Pu values, can be contacted with a cation exchange resin causing the Pu values to load the resin. The Pu values are selectively eluted from the resin with more concentrated HI.

Vondra, Benedict L. (Oak Ridge, TN); Tallent, Othar K. (Oak Ridge, TN); Mailen, James C. (Oak Ridge, TN)

1979-01-01T23:59:59.000Z

147

Utah Associated-Dissolved Natural Gas, Wet After Lease Separation...  

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

Adjustments (Billion Cubic Feet) Utah Associated-Dissolved Natural Gas, Wet After Lease Separation, Reserves Adjustments (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3...

148

Utah Associated-Dissolved Natural Gas, Wet After Lease Separation...  

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

Acquisitions (Billion Cubic Feet) Utah Associated-Dissolved Natural Gas, Wet After Lease Separation, Reserves Acquisitions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3...

149

Utah Associated-Dissolved Natural Gas, Wet After Lease Separation...  

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

Extensions (Billion Cubic Feet) Utah Associated-Dissolved Natural Gas, Wet After Lease Separation, Reserves Extensions (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3...

150

Utah Associated-Dissolved Natural Gas, Wet After Lease Separation...  

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

Increases (Billion Cubic Feet) Utah Associated-Dissolved Natural Gas, Wet After Lease Separation, Reserves Revision Increases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2...

151

Utah Associated-Dissolved Natural Gas, Wet After Lease Separation...  

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

Reservoir Discoveries in Old Fields (Billion Cubic Feet) Utah Associated-Dissolved Natural Gas, Wet After Lease Separation, New Reservoir Discoveries in Old Fields (Billion Cubic...

152

Utah Associated-Dissolved Natural Gas, Wet After Lease Separation...  

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

Decreases (Billion Cubic Feet) Utah Associated-Dissolved Natural Gas, Wet After Lease Separation, Reserves Revision Decreases (Billion Cubic Feet) Decade Year-0 Year-1 Year-2...

153

,"Utah Associated-Dissolved Natural Gas Proved Reserves, Wet...  

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

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

154

Utah Associated-Dissolved Natural Gas, Reserves in Nonproducing...  

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

Reserves in Nonproducing Reservoirs, Wet (Billion Cubic Feet) Utah Associated-Dissolved Natural Gas, Reserves in Nonproducing Reservoirs, Wet (Billion Cubic Feet) Decade Year-0...

155

Utah Associated-Dissolved Natural Gas, Wet After Lease Separation...  

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

Field Discoveries (Billion Cubic Feet) Utah Associated-Dissolved Natural Gas, Wet After Lease Separation, New Field Discoveries (Billion Cubic Feet) Decade Year-0 Year-1 Year-2...

156

Utah Associated-Dissolved Natural Gas, Wet After Lease Separation...  

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

Estimated Production from Reserves (Billion Cubic Feet) Utah Associated-Dissolved Natural Gas, Wet After Lease Separation, Estimated Production from Reserves (Billion Cubic Feet)...

157

,"Utah Associated-Dissolved Natural Gas, Wet After Lease Separation...  

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

,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","Utah Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion...

158

,"Louisiana State Offshore Associated-Dissolved Natural Gas,...  

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

Of Series","Frequency","Latest Data for" ,"Data 1","Louisiana State Offshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves...

159

,"California Federal Offshore Associated-Dissolved Natural Gas...  

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

Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","California Federal Offshore Associated-Dissolved Natural Gas, Wet After Lease Separation,...

160

,"California - San Joaquin Basin Onshore Associated-Dissolved...  

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

Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","California - San Joaquin Basin Onshore Associated-Dissolved Natural Gas, Wet After Lease...

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

,"California - Coastal Region Onshore Associated-Dissolved Natural...  

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

Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","California - Coastal Region Onshore Associated-Dissolved Natural Gas, Wet After Lease...

162

,"California State Offshore Associated-Dissolved Natural Gas...  

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

Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","California State Offshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved...

163

,"California Associated-Dissolved Natural Gas, Wet After Lease...  

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

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

164

,"California - Los Angeles Basin Onshore Associated-Dissolved...  

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

Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","California - Los Angeles Basin Onshore Associated-Dissolved Natural Gas, Wet After Lease...

165

,"Ohio Associated-Dissolved Natural Gas, Wet After Lease Separation...  

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

,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","Ohio Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion...

166

Texas State Offshore Associated-Dissolved Natural Gas, Wet After...  

Annual Energy Outlook 2012 (EIA)

Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Texas State Offshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved...

167

,"Michigan Associated-Dissolved Natural Gas, Wet After Lease...  

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

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

168

Texas - RRC District 3 Onshore Associated-Dissolved Natural Gas...  

Gasoline and Diesel Fuel Update (EIA)

Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Texas - RRC District 3 Onshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved...

169

Texas - RRC District 5 Associated-Dissolved Natural Gas, Wet...  

Gasoline and Diesel Fuel Update (EIA)

Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Texas - RRC District 5 Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved...

170

Texas - RRC District 8 Associated-Dissolved Natural Gas, Wet...  

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

Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Texas - RRC District 8 Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved...

171

Texas - RRC District 9 Associated-Dissolved Natural Gas, Wet...  

Gasoline and Diesel Fuel Update (EIA)

Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Texas - RRC District 9 Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved...

172

Texas - RRC District 6 Associated-Dissolved Natural Gas, Wet...  

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

Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Texas - RRC District 6 Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved...

173

,"Ohio Associated-Dissolved Natural Gas Proved Reserves, Wet...  

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

,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","Ohio Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease...

174

,"Colorado Associated-Dissolved Natural Gas, Wet After Lease...  

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

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

175

Oxidation Behavior of the Simulated Fuel with Dissolved ...  

Science Conference Proceedings (OSTI)

Page 1. Oxidation Behavior of the Simulated Fuel with Dissolved Fission Products in Air at 573~873 K KH Kang C, S, KC ...

2006-07-20T23:59:59.000Z

176

,"Texas Associated-Dissolved Natural Gas, Wet After Lease Separation...  

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

,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","Texas Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion...

177

,"Texas State Offshore Associated-Dissolved Natural Gas, Wet...  

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

,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","Texas State Offshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved...

178

,"Texas - RRC District 5 Associated-Dissolved Natural Gas, Wet...  

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

,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","Texas - RRC District 5 Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved...

179

,"Texas - RRC District 10 Associated-Dissolved Natural Gas, Wet...  

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

,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","Texas - RRC District 10 Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved...

180

,"Texas - RRC District 2 Onshore Associated-Dissolved Natural...  

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

,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","Texas - RRC District 2 Onshore Associated-Dissolved Natural Gas, Wet After Lease Separation,...

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

,"Texas - RRC District 4 Onshore Associated-Dissolved Natural...  

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

,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","Texas - RRC District 4 Onshore Associated-Dissolved Natural Gas, Wet After Lease Separation,...

182

,"Texas - RRC District 9 Associated-Dissolved Natural Gas, Wet...  

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

,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","Texas - RRC District 9 Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved...

183

,"Texas - RRC District 1 Associated-Dissolved Natural Gas, Wet...  

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

,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","Texas - RRC District 1 Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved...

184

,"Texas - RRC District 8 Associated-Dissolved Natural Gas, Wet...  

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

,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","Texas - RRC District 8 Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved...

185

,"Texas - RRC District 6 Associated-Dissolved Natural Gas, Wet...  

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

,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","Texas - RRC District 6 Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved...

186

Influence of temperature, moisture, and organic carbon on the flux of H/sub 2/ and CO between soil and atmosphere: field studies in subtropical regions  

Science Conference Proceedings (OSTI)

Production and deposition rates of atmospheric hydrogen and carbon monoxide were studied during field measurements in subtropical regions, i.e., Transvaal (South Africa), Andalusia (Spain), and the Karoo (South Africa). Measurements were carried out by applying static and equilibrium box techniques. The equilibrium technique has been introduced as a novel method to measure production and destruction rates simultaneously even when soil conditions (e.g., temperature) change during the course of the measurements. Deposition velocities of H/sub 2/ and CO were virtually independent of the soil temperature measured in 3- to 10-mm depths and agreed with those measured in the temperate regions. The deposition velocities were inhibited or stimulated by irrigation water depending on the conditions of the individual field sites. H/sub 2/ production by soil was not observed. By contrast, CO was produced by soil in a dark chemical reaction. Production rates increased exponentially with soil temperatures, giving activation energies of 57-110 kJ mol/sup -1/ and increased linearly with soil organic carbon content. CO production rates followed a diel rhythm parallel to soil surface temperatures. Production generally exceeded CO deposition during the hot hours of the day, so that arid subtropical soils act as a net source of atmospheric CO during this time. On a global basis, CO production by soil may reach source strengths of 30 Tg yr/sup -1/, which is considerably less than the global deposition of CO estimated to be 190-580 Tg yr/sup -1/. Global H/sub 2/ deposition rates were estimated to 70-110 Tg yr/sup -1/.

Conrad, R.; Seiler, W.

1985-06-20T23:59:59.000Z

187

Tracing And Quantifying Magmatic Carbon Discharge In Cold Groundwaters...  

Open Energy Info (EERE)

waters contain magmatic helium with 3He4He ratios as high as 4.5 times the atmospheric ratio, and a magmatic component in the dissolved inorganic carbon (DIC) can be identified in...

188

Maintaining and Monitoring Dissolved Oxygen at Hydroelectric Projects: Status Report  

Science Conference Proceedings (OSTI)

This report is an update of EPRI's 1990 report, "Assessment and Guide for Meeting Dissolved Oxygen Water Quality Standards for Hydroelectric Plant Discharges" (GS-7001). The report provides an updated review of technologies and techniques for enhancing dissolved oxygen (DO) levels in reservoirs and releases from hydroelectric projects and state-of-the-art methods, equipment, and techniques for monitoring DO.

2002-05-28T23:59:59.000Z

189

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

Moore, Keith

190

Carbon Accounting in Forest Ecosystems  

E-Print Network (OSTI)

. Carbon Pools: Above ground biomass Belowground BiomassBelowground Biomass Soil Organic Carbon Dead: · Aboveground biomassAboveground biomass · Belowground biomass · Soil Organic Carbon · Litter · Dead Wood· Dead Wood · (Wood Products) T�V S�D Industrie Service GmbH #12;Principles · Biomass is usually measured

Pettenella, Davide

191

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

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Alabama Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 13 1980's 23 25 1990's 25 23 30 46 56 44 38 30 28 27 2000's 29 26 31 32 32 29 18 20 19 29 2010's 38 48 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease Separation, as of Dec. 31 Alabama Associated-Dissolved Natural Gas Proved Reserves, Wet After

192

Atmospheric Plasma Deposition of Diamond-like Carbon Coatings  

DOE Green Energy (OSTI)

DLC coatings in a low-pressure environment. For example, ion beam processes are widely utilized since the ion bombardment is thought to promote denser sp3-bonded carbon networks. Other processes, such as sputtering, are better suited for coating large parts [29,30,44]. However, the deposition of DLC in a vacuum system has several disadvantages, including high equipment cost and restrictions on the size and shape of material that may be treated. The deposition of DLC at atmospheric pressure has been demonstrated by several researchers. Izake, et al [53] and Novikov and Dymont [54] have demonstrated an electrochemical process that is carried out with organic compounds such as methanol and acetylene dissolved in ammonia. This process requires that the substrates be immersed in the liquid [53-54]. The atmospheric pressure deposition of DLC was also demonstrated by Kulik, et al. utilizing a plasma torch. However, this process requires operating temperatures in excess of 800 oC [55]. In this report, we investigate the deposition of diamond-like carbon films using a low temperature, atmospheric pressure plasma-enhanced chemical vapor deposition (PECVD) process. The films were characterized by solid-state carbon-13 nuclear magnetic resonance (13C NMR) and found to have a ratio of sp2 to sp3 carbon of 43 to 57%. The films were also tested for adhesion, coefficient of friction, and dielectric strength.

Ladwig, Angela

2008-01-23T23:59:59.000Z

193

Hierarchical Template of Porous Carbon for Multifunctional ...  

Science Conference Proceedings (OSTI)

Hierarchical Template of Porous Carbon for Multifunctional Applications · Interstitial Hydride ... Structurally Dynamic Metal Organic Frameworks for CO2 Capture.

194

Terrestrial Carbon Management  

NLE Websites -- All DOE Office Websites (Extended Search)

Terrestrial Carbon Management Data Sets and Analyses Terrestrial Carbon Management Data Sets and Analyses Carbon Accumulation with Cropland Management Influence of Agricultural Management on Soil Organic Carbon: A Compendium and Assessment of Canadian Studies (VandenBygaart et al., Agriculture and Agri-Food Canada) Soil Carbon Sequestration by Tillage and Crop Rotation: A Global Data Analysis (West and Post, Oak Ridge National Laboratory) Preliminary Estimates of the Potential for Carbon Mitigation in European Soils Through No-Till Farming (Smith et al., University of Aberdeen, United Kingdom) Potential for Carbon Sequestration in European Soils: Preliminary Estimates for Five Scenarios Using Results from Long-Term Experiments (Smith et al., University of Aberdeen, United Kingdom) Carbon Accumulation with Grassland Management

195

California - Coastal Region Onshore Associated-Dissolved Natural Gas, Wet  

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) California - Coastal Region Onshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 307 1980's 265 265 325 344 256 254 261 243 220 233 1990's 228 220 196 135 145 109 120 129 116 233 2000's 244 185 197 173 188 269 208 211 150 168 2010's 178 172 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease

196

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

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Montana Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 51 1980's 122 89 81 108 77 91 98 97 101 68 1990's 86 66 61 53 55 53 51 42 52 67 2000's 70 85 94 112 130 161 195 219 197 312 2010's 302 270 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease Separation, as of Dec. 31

197

Louisiana - North Associated-Dissolved Natural Gas, Wet After Lease  

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Louisiana - North Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 765 1980's 916 1,040 832 775 690 632 567 488 249 237 1990's 241 192 160 120 134 133 255 287 183 260 2000's 186 168 159 139 107 98 90 73 78 53 2010's 73 98 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease

198

Utah Associated-Dissolved Natural Gas, Wet After Lease Separation...  

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

Sales (Billion Cubic Feet) Utah Associated-Dissolved Natural Gas, Wet After Lease Separation, Reserves Sales (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5...

199

California - Los Angeles Basin Onshore Associated-Dissolved Natural Gas,  

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

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) California - Los Angeles Basin Onshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 175 1980's 207 162 103 114 162 185 149 155 158 141 1990's 110 120 100 108 108 115 112 143 153 174 2000's 203 194 218 196 184 186 161 154 81 91 2010's 92 102 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease

200

California Federal Offshore Associated-Dissolved Natural Gas, Wet After  

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

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) California Federal Offshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 249 1980's 307 1,110 1,249 1,312 1,252 1990's 1,229 995 987 976 1,077 1,195 1,151 498 437 488 2000's 500 490 459 456 412 776 756 752 702 731 2010's 722 711 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease

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

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

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Michigan Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 733 1980's 883 758 719 824 774 689 577 569 491 432 1990's 408 437 352 328 357 326 347 281 228 227 2000's 214 159 214 269 193 153 192 179 148 77 2010's 72 77 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease Separation, as of Dec. 31

202

Miscellaneous States Associated-Dissolved Natural Gas, Wet After Lease  

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Miscellaneous States Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 14 1980's 34 12 27 31 14 25 41 13 28 39 1990's 22 14 11 9 11 32 28 31 17 54 2000's 19 19 20 14 12 14 19 15 9 78 2010's 10 104 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease Separation, as of Dec. 31

203

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

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Wyoming Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 1,038 1980's 1,374 1,228 1,060 959 867 710 691 691 616 581 1990's 573 572 624 502 611 879 824 850 794 713 2000's 652 488 561 450 362 384 347 365 223 362 2010's 334 318 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease

204

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

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Arkansas Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 166 1980's 194 184 174 194 189 157 150 145 157 145 1990's 67 136 133 93 85 104 89 56 38 41 2000's 39 30 38 37 40 46 44 37 12 20 2010's 29 46 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease Separation, as of Dec. 31

205

Program on Technology Innovation: Novel Carbon Sorbents  

Science Conference Proceedings (OSTI)

A new approach has been developed for making activated carbons and catalytic carbons with high surface areas. A novel carbonization process using alkali organic and metal salt precursors can yield carbons with a narrow, customized, pore size distribution as well as high adsorption capacity and catalytic activity. This report summarizes initial attempts to produce high-surface-area carbons with porous structure and carbons with added nanoscale catalyst using the novel carbonization process.

2009-03-23T23:59:59.000Z

206

Continuous surface ocean measurements of dissolved oxygen isotopes  

E-Print Network (OSTI)

Climate effects on atmospheric carbon dioxide over the lastNitrogen . . . . . . 3.3.2 Carbon dioxide . . 3.3.3 Wateron atmo- spheric carbon dioxide over the last century.

Rafelski, Lauren Elmegreen

2012-01-01T23:59:59.000Z

207

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

208

STOCK AND DISTRIBUTION OF TOTAL AND CORN-DERIVED SOIL ORGANIC CARBON IN AGGREGATE AND PRIMARY PARTICLE FRACTIONS FOR DIFFERENT LAND USE AND SOIL MANAGEMENT PRACTICES  

Science Conference Proceedings (OSTI)

Land use, soil management, and cropping systems affect stock, distribution, and residence time of soil organic carbon (SOC). Therefore, SOC stock and its depth distribution and association with primary and secondary particles were assessed in long-term experiments at the North Appalachian Experimental Watersheds near Coshocton, Ohio, through *13C techniques. These measurements were made for five land use and soil management treatments: (1) secondary forest, (2) meadow converted from no-till (NT) corn since 1988, (3) continuous NT corn since 1970, (4) continuous NT corn-soybean in rotation with ryegrass since 1984, and (5) conventional plow till (PT) corn since 1984. Soil samples to 70-cm depth were obtained in 2002 in all treatments. Significant differences in soil properties were observed among land use treatments for 0 to 5-cm depth. The SOC concentration (g C kg*1 of soil) in the 0 to 5-cm layer was 44.0 in forest, 24.0 in meadow, 26.1 in NT corn, 19.5 in NT corn-soybean, and 11.1 i n PT corn. The fraction of total C in corn residue converted to SOC was 11.9% for NT corn, 10.6% for NT corn-soybean, and 8.3% for PT corn. The proportion of SOC derived from corn residue was 96% for NT corn in the 0 to 5-cm layer, and it decreased gradually with depth and was 50% in PT corn. The mean SOC sequestration rate on conversion from PT to NT was 280 kg C ha*1 y*1. The SOC concentration decreased with reduction in aggregate size, and macro-aggregates contained 15 to 35% more SOC concentration than microaggregates. In comparison with forest, the magnitude of SOC depletion in the 0 to 30-cm layer was 15.5 Mg C/ha (24.0%) in meadow, 12.7 Mg C/ha (19.8%) in NT corn, 17.3 Mg C/ha (26.8%) in NT corn-soybean, and 23.3 Mg C/ha (35.1%) in PT corn. The SOC had a long turnover time when located deeper in the subsoil.

Puget, P; Lal, Rattan; Izaurralde, R Cesar C.; Post, M; Owens, Lloyd

2005-04-01T23:59:59.000Z

209

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

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Kentucky Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 2 1980's 11 14 12 19 17 13 17 19 19 22 1990's 8 10 8 6 47 27 24 26 20 29 2000's 27 25 25 25 19 30 36 34 34 32 2010's 111 98 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease Separation, as of Dec. 31 Kentucky Associated-Dissolved Natural Gas Proved Reserves, Wet After

210

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

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Florida Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 108 1980's 122 99 86 64 90 81 69 62 69 57 1990's 53 45 55 59 117 110 119 112 106 100 2000's 93 96 102 92 88 87 50 110 1 7 2010's 30 2 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease Separation, as of Dec. 31 Florida Associated-Dissolved Natural Gas Proved Reserves, Wet After

211

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

Science Conference Proceedings (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

212

Considerations for additional 321 Building mercury dissolving studies  

DOE Green Energy (OSTI)

Studies in the 321 Building dissolver during December 1953 and January 1954, were successful in developing a laboratory-proved mercury-catalyzed dissolving flowsheet into a suitable plant procedure. However, this flowsheet was not adapted for Redox plant operation because of uncertainty about the possible presence of hydrogen above the lower explosive limit in the off-gases. Subsequent laboratory work has resulted in a better understanding of the hydrogen evolution, and has resulted in developing low hydrogen evolution flowsheets. When one of these flowsheets is selected for further work, it will be tested in the 321 Building dissolver with non-irradiated slugs to provide information for scaling-up the single-slug laboratory data to a plant-scale operation. It is the purpose of this memorandum to outline the factors considered to be pertinent to the 321 Building investigation, to be used as a guide in making preparations for the runs to be performed.

Curtis, M.H.

1954-08-11T23:59:59.000Z

213

The Effects of Dissolved Methane upon Liquid Argon Scintillation Light  

E-Print Network (OSTI)

In this paper we report on measurements of the effects of dissolved methane upon argon scintillation light. We monitor the light yield from an alpha source held 20 cm from a cryogenic photomultiplier tube (PMT) assembly as methane is injected into a high-purity liquid argon volume. We observe significant suppression of the scintillation light yield by dissolved methane at the 10 part per billion (ppb) level. By examining the late scintillation light time constant, we determine that this loss is caused by an absorption process and also see some evidence of methane-induced scintillation quenching at higher concentrations (50-100 ppb). Using a second PMT assembly we look for visible re-emission features from the dissolved methane which have been reported in gas-phase argon methane mixtures, and we find no evidence of visible re-emission from liquid-phase argon methane mixtures at concentrations between 10 ppb and 0.1%.

B. J. P. Jones; T. Alexander; H. O. Back; G. Collin; J. M. Conrad; A. Greene; T. Katori; S. Pordes; M. Toups

2013-08-16T23:59:59.000Z

214

Philippines-Low Carbon Plan (LCP) | Open Energy Information  

Open Energy Info (EERE)

Philippines-Low Carbon Plan (LCP) Jump to: navigation, search Name Philippines-Low Carbon Plan (LCP) AgencyCompany Organization World Wildlife Fund Sector Energy Topics...

215

Total Dissolved Methylmercury Concentrations in Two Headwater Streams  

Science Conference Proceedings (OSTI)

Methylmercury (MeHg) is the only form of mercury whose concentrations increase with trophic level in aquatic food webs. As a consequence, a direct causal link exists between the levels of MeHg dissolved in water, where it typically accounts for only 10% of the total mercury, and in fish tissues, where it typically accounts for more than 90% of the total mercury. This link makes dissolved MeHg a critical indicator of an ecosystempotential to attain high fish mercury levels and makes its accurate measureme...

2009-11-20T23:59:59.000Z

216

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

DOE Data Explorer (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.

217

The effect of elevated atmospheric carbon dioxide mixing ratios on the emission of Volatile organic compounds from Corymbia citriodora and Tristaniopsis laurina.  

E-Print Network (OSTI)

??Bibliography: p. 120-124. Introduction  – Environmental factors affecting the emission of biogenic Volatile organic compounds  – Materials and experimental procedures  – Quantification using sold-phase microextraction… (more)

Camenzuli, Michelle

2008-01-01T23:59:59.000Z

218

PRODUCTION OF CARBON PRODUCTS USING A COAL EXTRACTION PROCESS  

Science Conference Proceedings (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

219

NETL: Carbon Storage - Big Sky Carbon Sequestration Partnership  

NLE Websites -- All DOE Office Websites (Extended Search)

BSCSP BSCSP Carbon Storage Big Sky Carbon Sequestration Partnership MORE INFO Additional information related to ongoing BSCSP efforts can be found on their website. The Big Sky Carbon Sequestration Partnership (BSCSP) is led by Montana State University-Bozeman and represents a coalition of more than 60 organizations including universities, national laboratories, private companies, state agencies, Native American tribes, and international collaborators. The partners are engaged in several aspects of BSCSP projects and contribute to the efforts to deploy carbon storage projects in the BSCSP region. The BSCSP region encompasses Montana, Wyoming, Idaho, South Dakota, and eastern Washington and Oregon. BSCSP Big Sky Carbon Sequestration Partnership Region Big Sky Carbon Sequestration Partnership Region

220

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

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) California Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 2,961 1980's 3,345 2,660 2,663 2,546 2,507 1990's 2,400 2,213 2,093 1,982 1,698 1,619 1,583 1,820 1,879 2,150 2000's 2,198 1,922 1,900 1,810 2,006 2,585 2,155 2,193 1,917 2,314 2010's 2,282 2,532 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease

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.


221

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

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Louisiana Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1980's 3,360 2,391 2,128 1,794 1,741 1990's 1,554 1,394 1,167 926 980 1,001 1,039 1,016 911 979 2000's 807 796 670 586 557 588 561 641 1,235 1,072 2010's 679 639 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease Separation, as of Dec. 31

222

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

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Colorado Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 181 1980's 200 259 206 173 208 167 190 219 177 236 1990's 510 682 762 1,162 1,088 1,072 1,055 533 772 781 2000's 960 1,025 1,097 1,186 1,293 1,326 1,541 1,838 2,010 1,882 2010's 2,371 2,518 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease

223

PROCESS OF DISSOLVING FUEL ELEMENTS OF NUCLEAR REACTORS  

DOE Patents (OSTI)

A process is described for dissolving stainless-steelor zirconium-clad uranium dioxide fuel elements by immersing the elements in molten lead chloride, adding copper, cuprous chloride, or cupric chloride as a catalyst and passing chlorine through the salt mixture. (AEC)

Wall, E.M.V.; Bauer, D.T.; Hahn, H.T.

1963-09-01T23:59:59.000Z

224

CarbonSolve | Open Energy Information  

Open Energy Info (EERE)

CarbonSolve CarbonSolve Jump to: navigation, search Tool Summary LAUNCH TOOL Name: CarbonSolve Agency/Company /Organization: CarbonSolve Sector: Climate Focus Area: Greenhouse Gas Resource Type: Software/modeling tools User Interface: Website Website: www.carbonsolve.com Web Application Link: www.carbonsolve.com Cost: Paid CarbonSolve Screenshot References: CarbonSolve[1] Logo: CarbonSolve The CarbonSolve platform is designed to address a broad spectrum of needs, and makes possible for organizations to transform their sustainability objectives - including carbon, water, waste, employee engagement, or supply chain related initiatives into measureable metrics and trackable processes. Overview The CarbonSolve platform is designed to address a broad spectrum of needs, and makes possible for organizations to transform their sustainability

225

Dynamics of organic matter production and degradation during coastal diatom blooms.  

E-Print Network (OSTI)

??Experiments were designed to answer key questions about diatom-derived organic matter cycling (i.e., production and degradation) in coastal systems. Dissolved organic matter (DOM) production was… (more)

[No author

2006-01-01T23:59:59.000Z

226

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

DOE Green Energy (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

227

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

228

How Dissolved Metal Ions Interact in Solution | Advanced Photon Source  

NLE Websites -- All DOE Office Websites (Extended Search)

One Giant Leap for Radiation Biology? One Giant Leap for Radiation Biology? What's in the Cage Matters in Iron Antimonide Thermoelectric Materials Novel Experiments on Cement Yield Concrete Results Watching a Glycine Riboswitch "Switch" Polyamorphism in a Metallic Glass Science Highlights Archives: 2013 | 2012 | 2011 | 2010 2009 | 2008 | 2007 | 2006 2005 | 2004 | 2003 | 2002 2001 | 2000 | 1998 | Subscribe to APS Science Highlights rss feed How Dissolved Metal Ions Interact in Solution MAY 2, 2007 Bookmark and Share Researchers at the Department of Energy's Argonne National Laboratory and the University of Notre Dame have successfully applied X-ray scattering techniques to determine how dissolved metal ions interact in solution. Researchers from the U.S. Department of Energy's Argonne National

229

California - San Joaquin Basin Onshore Associated-Dissolved Natural Gas,  

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) California - San Joaquin Basin Onshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 2,253 1980's 2,713 2,664 2,465 2,408 2,270 2,074 2,006 2,033 1,947 1,927 1990's 1,874 1,818 1,738 1,676 1,386 1,339 1,304 1,494 1,571 1,685 2000's 1,665 1,463 1,400 1,365 1,549 2,041 1,701 1,749 1,632 2,002 2010's 1,949 2,179 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014

230

NETL: Carbon Storage - Southeast Regional Carbon Sequestration Partnership  

NLE Websites -- All DOE Office Websites (Extended Search)

Southeast Regional Carbon Sequestration Partnership Southeast Regional Carbon Sequestration Partnership MORE INFO Additional information related to ongoing SECARB efforts can be found on their website. The Southeast Regional Carbon Sequestration Partnership (SECARB), managed by the Southern States Energy Board (SSEB), represents a 13-State region, including Alabama, Arkansas, Florida, Georgia, Louisiana, Mississippi, North Carolina, South Carolina, Tennessee, Texas, and Virginia, and portions of Kentucky and West Virginia. SECARB is comprised of over 100 participants representing Federal and State governments, industry, academia, and non-profit organizations. Southeast Regional Carbon Sequestration Partnership Region Southeast Regional Carbon Sequestration Partnership Region The primary goal of SECARB is to develop the necessary framework and

231

CARBON-CARBON COMPOSITE ALLCOMP Carbon-Carbon Composite  

E-Print Network (OSTI)

strength 4340 steel, carbon-carbon composite, and Carbon-Silicon Carbide composite were tested to examine-C composite containing continuous PAN T300 fibers · SWB: Chopped Fiber Composite containing SWB fibers Crush

Rollins, Andrew M.

232

013 Characterization of the Sintered Porous Zirconia Dissolves the ...  

Science Conference Proceedings (OSTI)

Porous zirconia was synthesized in order to overcome this problem. To avoid .... 166 Multi-Phase-Field Simulation in a Low Carbon Steel for Continuous Cooling  ...

233

Carbon Jungle | Open Energy Information  

Open Energy Info (EERE)

Jungle Jungle Jump to: navigation, search Name Carbon Jungle Place El Segundo, California Zip 90246 Sector Carbon Product Carbon Jungle's mission is to decrease CO2 in the atmosphere by planting and managing tree plantations, increasing awareness of the facts behind increased CO2 in the atmosphere, and giving companies a means to participate in carbon credit trading. References Carbon Jungle[1] LinkedIn Connections CrunchBase Profile No CrunchBase profile. Create one now! This article is a stub. You can help OpenEI by expanding it. Carbon Jungle is a company located in El Segundo, California . References ↑ "Carbon Jungle" Retrieved from "http://en.openei.org/w/index.php?title=Carbon_Jungle&oldid=343237" Categories: Clean Energy Organizations

234

Energy-efficient indoor volatile organic compound air cleaning...  

NLE Websites -- All DOE Office Websites (Extended Search)

Energy-efficient indoor volatile organic compound air cleaning using activated carbon fiber media with nightly regeneration Title Energy-efficient indoor volatile organic compound...

235

Global climate change and pedogenic carbonates  

SciTech Connect

Global Climate Change summarizes what is known about soil inorganic carbon and develops strategies that could lead to the retention of more carbon in the soil. It covers basic concepts, analytical methods, secondary carbonates, and research and development priorities. With this book one will get a better understanding of the global carbon cycle, organic and inorganic carbon, and their roles, or what is known of them, in the greenhouse effect.

Lal, R.; Kimble, J.M.; Stewart, B.A.; Eswaran, H. [eds.

1999-11-01T23:59:59.000Z

236

Methods and systems for chemoautotrophic production of organic compounds  

SciTech Connect

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

237

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

Science Conference Proceedings (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

238

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

SciTech Connect

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

239

NETL: News Release - Carbon Sequestration Regional Partnership...  

NLE Websites -- All DOE Office Websites (Extended Search)

June 10, 2004 Carbon Sequestration Regional Partnership Program Adds Partners Seven States, Thirteen Organizations Added; Will Help Develop Sequestration Options WASHINGTON, DC -...

240

Multiphase Sequestration Geochemistry: Model for Mineral Carbonation  

SciTech Connect

Carbonation of formation minerals converts low viscosity supercritical CO2 injected into deep saline reservoirs for geologic sequestration into an immobile form. Until recently the scientific focus of mineralization reactions with reservoir rocks has been those that follow an aqueous-mediated dissolution/precipitation mechanism, driven by the sharp reduction in pH that occurs with CO2 partitioning into the aqueous phase. For sedimentary basin formations the kinetics of aqueous-mediated dissolution/precipitation reactions are sufficiently slow to make the role of mineralization trapping insignificant over a century period. For basaltic saline formations aqueous-phase mineralization progresses at a substantially higher rate, making the role of mineralization trapping significant, if not dominant, over a century period. The overlooked mineralization reactions for both sedimentary and basaltic saline formations, however, are those that occur in liquid or supercritical CO2 phase; where, dissolved water appears to play a catalyst role in the formation of carbonate minerals. A model is proposed in this paper that describes mineral carbonation over sequestration reservoir conditions ranging from dissolved CO2 in aqueous brine to dissolved water in supercritical CO2. The model theory is based on a review of recent experiments directed at understanding the role of water in mineral carbonation reactions of interest in geologic sequestration systems occurring under low water contents.

White, Mark D.; McGrail, B. Peter; Schaef, Herbert T.; Hu, Jian Z.; Hoyt, David W.; Felmy, Andrew R.; Rosso, Kevin M.; Wurstner, Signe K.

2011-04-01T23:59:59.000Z

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.


241

Secondary Organic Aerosol Formation From Radical-Initiated Reactions of Alkenes: Development of Mechanisms  

E-Print Network (OSTI)

and Secondary Organic Aerosols in Southern California duringSources of Organic Carbon Aerosols in the Free Troposphere21 co-authors), 2005. Organic Aerosol and Global Climate

Matsunaga, Aiko

2009-01-01T23:59:59.000Z

242

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

SciTech Connect

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

243

CARBON TETRACHLORIDE  

E-Print Network (OSTI)

This fact sheet answers the most frequently asked health questions (FAQs) about carbon tetrachloride.

unknown authors

2005-01-01T23:59:59.000Z

244

A spatial deconvolution of molecular signals in oceanic dissolved organic matter  

E-Print Network (OSTI)

power of radiocarbon in biogeochemical studies of the marinepower of radiocarbon in biogeochemical studies of the marine

Meador, Travis Blake

2008-01-01T23:59:59.000Z

245

A Spatial Deconvolution of Molecular Signals in Oceanic Dissolved Organic Matter  

E-Print Network (OSTI)

power of radiocarbon in biogeochemical studies of the marinepower of radiocarbon in biogeochemical studies of the marine

Meador, Travis B

2008-01-01T23:59:59.000Z

246

The Use of Stable and Radiocarbon Isotopes as a Method for Delineating Sources of Organic Matter in Anchialine Systems  

E-Print Network (OSTI)

Submerged caves, locally referred to as cenotes, can be found throughout the Yucatan Peninsula of Mexico. These nutrient poor, aphotic “underground estuaries” lack photosynthetic primary productivity, but are often found underlying high primary productivity areas such as mangroves and tropical forests. Adjacent ecosystems contribute organic carbon to the cave systems via percolation, where it is then utilized by the obligate, cave-dwelling fish and invertebrates. Another potential pathway through which organic carbon can enter the cave food web is through chemosynthesis. Chemoautotrophic sulfur-oxidizing or nitrifying bacteria have been found in the hydrogen sulfide layer or in the sediments of some anchialine caves. Our study utilizes 13C/12C and 15N/14N stable isotopes as well as 14C radiocarbon dating to determine and compare the sources of organic matter entering a coastal anchialine cave (Cenote Aak Kimin) versus an inland cave (Cenote Maya Blue) in the Yucatan Peninsula. Stable isotopes have long been employed in tropic investigations. This study, however, is the first to utilize radiocarbon isotopes in anchialine caves. The use of both stable and radiocarbon isotopes as source indicators provides greater discrimination in systems that contain numerous carbon sources or indistinct trophic levels, particularly to distinguish between chemoautotrophic versus photosynthetically derived carbon. Results indicate that chemosynthetically derived organic carbon contributes substantially to the diet of some crustaceans, such as the stygobitic shrimp Typhlatya, while other species remain dependent on detrital inputs. Depleted ?13C values and aged radiocarbon values (as low as -47.51‰ and 1840 yrs. for Typhlatya spp.) in comparison to particulate and sediment ?13C values (lowest -32.07‰ and -28.43‰, respectively). A comparison of isotopic values between Cenote Aak Kimin and Cenote Maya Blue suggests that the trophic web of the coastal cave incorporates more photosynthetic or detrital carbon, while the inland cave, with more depleted 13C and 14C values, relies more heavily on chemoautotrophic carbon. Within both systems, however, distinct photosynthetic and chemoautotrophic levels were identified. Water quality parameters, especially dissolved oxygen and pH, support the hypothesis of bacterial activity at the halocline. Anchialine systems in the Yucatan Peninsula are threatened due to increases in tourism, development, and pollution. Quantifying and qualifying the inputs of organic carbon is vital for the management and conservation of the area’s freshwater resources.

Neisch, Julie A

2013-05-01T23:59:59.000Z

247

NETL: Carbon Storage  

NLE Websites -- All DOE Office Websites (Extended Search)

Carbon Sequestration Partnerships Regional Carbon Sequestration Partnership (RCSP) Programmatic Points of Contact Carbon Storage Program Infrastructure Coordinator Carbon Storage...

248

Impact of biochar application on nitrogen nutrition of rice, greenhouse-gas emissions and soil organic carbon dynamics in two paddy soils of China  

Science Conference Proceedings (OSTI)

Two field microcosm experiments and 15N labeling techniques were used to investigate the first-year effects of biochar addition on rice N nutrition and GHG emissions in an Inceptisol and an Ultisol. Biochar N bioavailability and effect of biochar on fertilizer nitrogen-use efficiency (NUE) were studied by 15N-enriched wheat biochar (7.8803 atom% 15N) and fertilizer urea (5 atom% 15N) (Experiment I). Corn biochar and corn stalks were applied at 12 Mg ha-1 to study their effects on GHG emissions (Experiment II). Biochar had no significant impact on rice production and less than 2% of the biochar N was available to plants in the first season. Biochar addition increased soil C and N contents and decreased urea NUE.. Seasonal cumulative CH4 emissions with biochar were similar to the controls, but significantly lower than the local practice of straw amendment. Soil emissions of N2O with biochar amendment were similar to the control in the acidic Ultisol, but significantly higher in the slightly alkaline Inceptisol. Carbon-balance calculations found no major losses of biochar-C. Low bio-availability of biochar N did not make a significant impact on rice production or N nutrition during the first year.. Replacement of straw amendments with biochar could decrease CH4 emissions and increase SOC stocks.

Xie, Zubin; Xu, Yanping; Liu, Gang; Liu, Qi; Zhu, Jianguo; Tu, Cong; Amonette, James E.; Cadisch, Georg; Yong, Jean W.; Hu, Shuijin

2013-09-01T23:59:59.000Z

249

Process for coal liquefaction by separation of entrained gases from slurry exiting staged dissolvers  

SciTech Connect

There is described an improved liquefaction process by which coal is converted to a low ash and low sulfur carbonaceous material that can be used as a fuel in an environmentally acceptable manner without costly gas scrubbing equipment. In the process, coal is slurried with a solvent, passed through a preheater and at least two dissolvers in series in the presence of hydrogen-rich gases at elevated temperatures and pressures. Solids, including mineral ash and unconverted coal macerals are separated from the condensed dissolver effluent. In accordance with the improved process, fresh hydrogen is fed to each dissolver and the entrained gas from each dissolver is separated from the slurry phase and removed from the reactor system before the condensed phase is passed to the next dissolver in the series. In accordance with another process, the feeds to the dissolvers are such that the top of each downstream dissolver is used as a gas-liquid separator.

Givens, Edwin N. (Bethlehem, PA); Ying, David H. S. (Macungie, PA)

1983-01-01T23:59:59.000Z

250

Nonaqueous method for dissolving lanthanide and actinide metals  

DOE Patents (OSTI)

Lanthanide and actinide beta-diketonate complex molecular compounds are produced by reacting a beta-diketone compound with a lanthanide or actinide element in the elemental metallic state in a mixture of carbon tetrachloride and methanol.

Crisler, L.R.

1975-11-11T23:59:59.000Z

251

Intelligent control aeration and external carbon addition for improving nitrogen removal  

Science Conference Proceedings (OSTI)

Fuzzy logic can in several ways be applied to improve the control of the activated sludge system. In this paper, fuzzy logic based control strategies for external carbon flow in the anoxic zone and dissolved oxygen (DO) concentration in the aerobic zone ... Keywords: Energy saving, External carbon addition, Fuzzy control, Nitrogen removal, Predenitrification process

M. Yong; P. Yong-zhen; W. Xiao-lian; W. Shu-ying

2006-06-01T23:59:59.000Z

252

Total Dissolved Gas Effects on Fishes of the Lower Columbia River  

DOE Green Energy (OSTI)

Gas supersaturation problems generated by spill from dams on the Columbia River were first identified in the 1960s. Since that time, considerable research has been conducted on effects of gas supersaturation on aquatic life, primarily juvenile salmonids. Also since that time, modifications to dam structures and operations have reduced supersaturated gas levels produced by the dams. The limit for total dissolved gas saturation (TDGS) as mandated by current Environmental Protection Agency water quality standards is 110%. State management agencies issue limited waivers to water quality, allowing production of levels of up to 120% TDGS to facilitate the downstream migration of juvenile salmonids. Recently, gas supersaturation as a water quality issue has resurfaced as concerns have grown regarding chronic effects of spill-related total dissolved gas on salmonids, including incubating embryos and larvae, resident fish species, and other aquatic organisms. Because of current concerns, and because the last comprehensive review of research on supersaturation effects on fishes was conducted in 1997, we reviewed recent supersaturation literature to identify new or ongoing issues that may not be adequately addressed by the current 110% TDGS limit and the 120% TDGS water quality waiver. We found that recent work supports older research indicating that short-term exposure to levels up to 120% TDGS does not produce acute effects on migratory juvenile or adult salmonids when compensating depths are available. Monitoring programs at Snake and Columbia river dams from 1995 to the early 2000s documented a low incidence of significant gas bubble disease or mortality in Columbia River salmonids, resident fishes, or other taxa. We did, however, identify five areas of concern in which total dissolved gas levels lower than water quality limits may produce sublethal effects on fishes of the Columbia River. These areas of concern are 1) sensitive and vulnerable species or life stages, 2) long-term chronic or multiple exposure, 3) vulnerable habitats and reaches, 4) effects on incubating fish in hyporheic habitats, and 5) community and ecosystem effects. Although some of these areas of concern may have been identified previously in earlier works, we suggest that consideration of the issues is warranted to avoid detrimental impacts on aquatic resources of the Columbia River system. We discuss these issues and provide recommendations to regulatory and management agencies based on our review of recent literature. In general, we recommend that additional attention be directed toward resolving the uncertainties within these five areas.

McGrath, Kathy E.; Dawley, Earl; Geist, David R.

2006-03-31T23:59:59.000Z

253

NETL: Carbon Storage - Midwest Regional Carbon Sequestration Partnership  

NLE Websites -- All DOE Office Websites (Extended Search)

MRCSP MRCSP Carbon Storage Midwest Regional Carbon Sequestration Partnership MORE INFO Additional information related to ongoing MRCSP efforts can be found on their website. The Midwest Regional Carbon Sequestration Partnership (MRCSP) was established to assess the technical potential, economic viability, and public acceptability of carbon storage within a region consisting of nine contiguous states: Indiana, Kentucky, Maryland, Michigan, New Jersey, New York, Ohio, Pennsylvania, and West Virginia. A group of leading universities, state geological surveys, non-governmental organizations and private companies, led by Battelle Memorial Institute, has been assembled to carry out this research. The MRCSP currently consists of nearly 40 members; each contributing technical knowledge, expertise and cost sharing.

254

Carbon and Nitrogen Dynamics in Agricultural Soils  

E-Print Network (OSTI)

Carbon and Nitrogen Dynamics in Agricultural Soils Model Applications at Different Scales in Time Print: SLU Service/Repro, Uppsala 2012 #12;Carbon and Nitrogen Dynamics in Agricultural Soils. Model Applications at Different Scales in Time and Space Abstract An understanding of soil organic carbon (C

255

On The Importance of Organic Oxygen for Understanding Organic Aerosol  

NLE Websites -- All DOE Office Websites (Extended Search)

On The Importance of Organic Oxygen for Understanding Organic Aerosol On The Importance of Organic Oxygen for Understanding Organic Aerosol Particles Title On The Importance of Organic Oxygen for Understanding Organic Aerosol Particles Publication Type Journal Article Year of Publication 2006 Authors Pang, Yanbo, B. J. Turpin, and Lara A. Gundel Journal Journal of Aerosol Science and Technology Volume 40 Start Page Chapter Pagination 128-133 Abstract This study shows how aerosol organic oxygen data could provide new and independent information about organic aerosol mass, aqueous solubility of organic aerosols, formation of secondary organic aerosol (SOA) and the relative contributions of anthropogenic and biogenic sources. For more than two decades atmospheric aerosol organic mass concentration has usually been estimated by multiplying the measured carbon content by an assumed organic mass (OM)-to-organic carbon (OC ) factor of 1.4. However, this factor can vary from 1.0 to 2.5 depending on location. This great uncertainty about aerosol organic mass limits our understanding of the influence of organic aerosol on climate, visibility and health.New examination of organic aerosol speciation data shows that the oxygen content is the key factor responsible for the observed range in the OM-to-OC factor. When organic oxygen content is excluded, the ratio of non-oxygen organic mass to carbon mass varies very little across different environments (1.12 to 1.14). The non-oxygen-OM-to-non-oxygen OC factor for all studied sites (urban and non-urban) is 1.13± 0.02. The uncertainty becomes an order of magnitude smaller than the uncertainty in the best current estimates of organic mass to organic carbon ratios (1.6± 0.2 for urban and 2.1± 0.2 for non-urban areas). When aerosol organic oxygen data become available, organic aerosol mass can be quite accurately estimated using just OC and organic oxygen (OO) without the need to know whether the aerosol is fresh or aged. In addition, aerosol organic oxygen data will aid prediction of water solubility since compounds with OO-to-OC higher than 0.4 have water solubilities higher than 1g per 100 g water

256

Interfacial Studies of Sized Carbon Fiber  

SciTech Connect

This study was performed to investigate the influence of sizing treatment on carbon fiber in respect of interfacial adhesion in composite materials, Epolam registered 2025. Fortafil unsized carbon fiber was used to performed the experiment. The fiber was commercially surface treated and it was a polyacrylonitrile based carbon fiber with 3000 filament per strand. Epicure registered 3370 was used as basic sizing chemical and dissolved in two types of solvent, ethanol and acetone for the comparison purpose. The single pull out test has been used to determine the influence of sizing on carbon fiber. The morphology of carbon fiber was observed by atomic force microscopy (AFM) and scanning electron microscopy (SEM). The apparent interfacial strength IFSS values determined by pull out test for the Epicure registered 3370/ethanol sized carbon fiber pointed to a good interfacial behaviour compared to the Epicure registered 3370/acetone sized carbon fiber. The Epicure registered 3370/ethanol sizing agent was found to be effective in promoting adhesion because of the chemical reactions between the sizing and Epolam registered 2025 during the curing process. From this work, it showed that sized carbon fiber using Epicure registered 3370 with addition of ethanol give higher mechanical properties of carbon fiber in terms of shear strength and also provided a good adhesion between fiber and matrix compared to the sizing chemical that contain acetone as a solvent.

Shahrul, S. N.; Hartini, M. N.; Hilmi, E. A.; Nizam, A. [Nanomaterials Program, Advance Materials Centre (AMREC), SIRIM Berhad, Lot 34, Jalan Hi-Tech Park, 09000, Kulim, Kedah (Malaysia)

2010-03-11T23:59:59.000Z

257

MST: Organizations: Organic Materials  

NLE Websites -- All DOE Office Websites (Extended Search)

Adhesive Bonding Adhesive Bonding Composites Encapsulation Materials Characterization Mechanical Testing Molding, Thermoforming, & Compounding Organizations Organic Materials Composite-to-metal adhesive bond Experimental/analytical study of composit-to-metal adhesive bond. The Organic Materials department in the Advanced Manufacturing and Processing Laboratory provides innovative prototype fabrication, full service small lot production, materials technology, processing expertise, and a broad range of organic material characterization and mechanical testing techniques. We encapsulate, we join and bond, we foam, we analyze and image, we build composite structures. We strive to make you, our customers, successful! We partner with you to find the right combination of materials, processing, and fixturing that will result in the highest value

258

Common Carbon Metric | Open Energy Information  

Open Energy Info (EERE)

Common Carbon Metric Common Carbon Metric Jump to: navigation, search Tool Summary Name: Common Carbon Metric Agency/Company /Organization: United Nations Environment Programme, World Resources Institute Sector: Energy Focus Area: Buildings, Energy Efficiency, Industry Topics: GHG inventory, Implementation Resource Type: Guide/manual, Publications Website: www.unep.org/sbci/pdfs/Common-Carbon-Metric-for_Pilot_Testing_220410.p Common Carbon Metric Screenshot References: Common Carbon Metrics [1] "This paper is offered by the United Nations Environment Programme's Sustainable Buildings & Climate Initiative (UNEP-SBCI), a partnership between the UN and public and private stakeholders in the building sector, promoting sustainable building practices globally. The purpose of this

259

Forest Carbon Portal | Open Energy Information  

Open Energy Info (EERE)

Forest Carbon Portal Forest Carbon Portal Jump to: navigation, search Tool Summary Name: Forest Carbon Portal Agency/Company /Organization: United Nations Development Programme, United States Agency for International Development, United Kingdom Department for International Development, Forest Trends Sector: Land Focus Area: Forestry Topics: GHG inventory Resource Type: Lessons learned/best practices Website: www.forestcarbonportal.com/ Forest Carbon Portal Screenshot References: FCP[1] "Ecosystem Marketplace's Forest Carbon Portal is a clearinghouse of information, feature stories, event listings, project details, 'how-to' guides, news, and market analysis on forest-based carbon sequestration projects. Deforestation and land-use change are responsible for 17% of the

260

Determination of free CO2 in emergent groundwaters using a commercial beverage carbonation meter  

Science Conference Proceedings (OSTI)

Dissolved CO{sub 2} in groundwater is frequently supersaturated relative to its equilibrium with atmospheric partial pressure and will degas when it is conveyed to the surface. Estimates of dissolved CO{sub 2} concentrations can vary widely between different hydrochemical facies because they have different sources of error (e.g., rapid degassing, low alkalinity, non-carbonate alkalinity). We sampled 60 natural spring and mine waters using a beverage industry carbonation meter, which measures dissolved CO{sub 2} based on temperature and pressure changes as the sample volume is expanded. Using a modified field protocol, the meter was found to be highly accurate in the range 0.2–35 mMCO{sub 2}. The meter provided rapid, accurate and precise measurements of dissolved CO{sub 2} in natural waters for a range of hydrochemical facies. Dissolved CO{sub 2} concentrations measured in the field with the carbonation meter were similar to CO{sub 2} determined using the pH-alkalinity approach, but provided immediate results and avoided errors from alkalinity and pH determination. The portability and ease of use of the carbonation meter in the field made it well-suited to sampling in difficult terrain. The carbonation meter has proven useful in the study of aquatic systems where CO{sub 2} degassing drives geochemical changes that result in surficial mineral precipitation and deposition, such as tufa, travertine and mine drainage deposits.

Vesper, Dorothy J.; Edenborn, Harry M.

2012-03-12T23:59:59.000Z

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.


261

Biogeochemical Behavior of Dissolved Arsenic and Uranium Concentrations in Public Water Supply Wells.  

E-Print Network (OSTI)

??Public water supply (PWS) wells currently contain dissolved uranium concentrations above the federally mandated maximum contaminant level (MCL) of 30 ppb (parts per billion) and… (more)

mcvey, kevin j

2009-01-01T23:59:59.000Z

262

,"U.S. Federal Offshore Associated-Dissolved Natural Gas, Wet...  

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

Of Series","Frequency","Latest Data for" ,"Data 1","U.S. Federal Offshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves...

263

Texas - RRC District 7B Associated-Dissolved Natural Gas, Wet...  

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

Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Texas - RRC District 7B Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved...

264

Texas - RRC District 8A Associated-Dissolved Natural Gas, Wet...  

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

Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Texas - RRC District 8A Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved...

265

Texas - RRC District 7C Associated-Dissolved Natural Gas, Wet...  

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

Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Texas - RRC District 7C Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved...

266

,"U.S. Associated-Dissolved Natural Gas Proved Reserves, Wet...  

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

,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","U.S. Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease...

267

,"Texas - RRC District 7B Associated-Dissolved Natural Gas, Wet...  

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

,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","Texas - RRC District 7B Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved...

268

,"Texas - RRC District 8A Associated-Dissolved Natural Gas, Wet...  

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

,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","Texas - RRC District 8A Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved...

269

,"Texas - RRC District 7C Associated-Dissolved Natural Gas, Wet...  

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

,"Worksheet Name","Description"," Of Series","Frequency","Latest Data for" ,"Data 1","Texas - RRC District 7C Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved...

270

Treatment of organic waste  

DOE Patents (OSTI)

An organic waste containing at least one element selected from the group consisting of strontium, cesium, iodine and ruthenium is treated to achieve a substantial reduction in the volume of the waste and provide for fixation of the selected element in an inert salt. The method of treatment comprises introducing the organic waste and a source of oxygen into a molten salt bath maintained at an elevated temperature to produce solid and gaseous reaction products. The gaseous reaction products comprise carbon dioxide and water vapor, and the solid reaction products comprise the inorganic ash constituents of the organic waste and the selected element which is retained in the molten salt. The molten salt bath comprises one or more alkali metal carbonates, and may optionally include from 1 to about 25 wt.% of an alkali metal sulfate.

Grantham, LeRoy F. (Calabasas, CA)

1979-01-01T23:59:59.000Z

271

Carbon Cycle  

NLE Websites -- All DOE Office Websites (Extended Search)

Carbon Cycle Carbon Cycle Latest Global Carbon Budget Estimates Including CDIAC Estimates Terrestrial Carbon Management Data Sets and Analyses Carbon Dioxide Emissions from Fossil-Fuel Consumption and Cement Manufacture, (2011) Annual Fossil-Fuel CO2 Emissions: Mass of Emissions Gridded by One Degree Latitude by One Degree Longitude (2012) Monthly Fossil-Fuel CO2 Emissions: Mass of Emissions Gridded by One Degree Latitude by One Degree Longitude (2012) Annual Fossil-Fuel CO2 Emissions: Global Stable Carbon Isotopic Signature (2012) Monthly Fossil-Fuel CO2 Emissions: Isomass (δ 13C) of Emissions Gridded by One Degree Latitude by One Degree Longitude (2012) AmeriFlux - Terrestrial Carbon Dioxide, Water Vapor, and Energy Balance Measurements Estimates of Monthly CO2 Emissions and Associated 13C/12C Values

272

Carbon Isotopes  

NLE Websites -- All DOE Office Websites (Extended Search)

Atmospheric Trace Gases » Carbon Isotopes Atmospheric Trace Gases » Carbon Isotopes Carbon Isotopes Gateway Pages to Isotopes Data Modern Records of Carbon and Oxygen Isotopes in Atmospheric Carbon Dioxide and Carbon-13 in Methane 800,000 Deuterium Record and Shorter Records of Various Isotopic Species from Ice Cores Carbon-13 13C in CO Measurements from Niwot Ridge, Colorado and Montana de Oro, California (Tyler) 13C in CO2 NOAA/CMDL Flask Network (White and Vaughn) CSIRO GASLAB Flask Network (Allison, Francey, and Krummel) CSIRO in situ measurements at Cape Grim, Tasmania (Francey and Allison) Scripps Institution of Oceanography (Keeling et al.) 13C in CH4 NOAA/CMDL Flask Network (Miller and White) Northern & Southern Hemisphere Sites (Quay and Stutsman) Northern & Southern Hemisphere Sites (Stevens)

273

Carbon Capture and Storage  

NLE Websites -- All DOE Office Websites (Extended Search)

SECARB's SECARB's Mississippi SalineTest Site: A Field Project Update Robert C. Trautz (rtrautz@epri.com) Electric Power Research Institute Senior Project Manager DOE Regional Carbon Sequestration Partnership Annual Review Meeting October 6-8, 2008 Pittsburgh, PA 2 1. Introduction 2. Well Drilling & Completion 3. Reservoir Characterization 4. CO 2 Injection Operations 5. Monitoring and Verification Outline 3 Key Organizations and Acknowledgments SOUTHERN STATES ENERGY BOARD Dr. Gerald (Jerry) R. Hill OTHER FIELD PROJECTS AND SUPPORTING ACTIVITIES * Advanced Resources * Alabama Geological Survey/ SCS * Gulf Coast Carbon Center (TXBEG) * EPRI * Virginia Tech University * Mississippi State University * Others Richard Esposito MISSISSIPPI POWER CO. Rick Berry Richard (Dick) Rhudy Robert (Rob) Trautz

274

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

275

Dissolving brittle stars hint at implications of ocean acidification |  

NLE Websites -- All DOE Office Websites (Extended Search)

Sea urchins and brittle starfish on the seabed at Explorers Cove in Antarctica. The rate the starfish decay offers clues to ocean acidification. Photo courtesy of Shawn Harper. To view a larger version of the image, click on it. Sea urchins and brittle starfish on the seabed at Explorers Cove in Antarctica. The rate the starfish decay offers clues to ocean acidification. Photo courtesy of Shawn Harper. To view a larger version of the image, click on it. Sea urchins and brittle starfish on the seabed at Explorers Cove in Antarctica. The rate the starfish decay offers clues to ocean acidification. Photo courtesy of Shawn Harper. To view a larger version of the image, click on it. Dissolving brittle stars hint at implications of ocean acidification By Chelsea Leu * August 15, 2013 Tweet EmailPrint Under the sea ice of Explorers Cove, Antarctica, is a startling array of life. Brittle stars, sea urchins and scallops grow in profusion on the seafloor, a stark contrast to the icy moonscape on the continent's

276

The Transfer of Dissolved Cs-137 from Soil to Plants  

SciTech Connect

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

277

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

Science Conference Proceedings (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

278

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

279

Time Series Measurements from a Moored Fluorescence-Based Dissolved Oxygen Sensor  

Science Conference Proceedings (OSTI)

We present an analysis of time-series measurements from a prototype fluorescence-quenching dissolved oxygen sensor moored for a six-day period in late March 1987 at 100 m depth in Saanich Inlet, British Columbia. Temporal variations in dissolved ...

Richard E. Thomson; Terrence A. Curran; M. Coreen Hamilton; Ronald McFarlane

1988-10-01T23:59:59.000Z

280

Carbon Nanotubes  

Science Conference Proceedings (OSTI)

Carbon Nanotubes. Sponsored by: TMS Electronic, Magnetic and Photonic Materials Division Date and Time: Sunday, February 13, 2005 ~ 8:30 am-5:00 pm

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

Carbon Nanomaterials  

Science Conference Proceedings (OSTI)

Mar 12, 2012 ... The graphene film was spin-coated using carbon nanotubes to form the cathode of the field emission device. A phosphor coated graphene-PET ...

282

Louisiana State Offshore Associated-Dissolved Natural Gas, Wet After Lease  

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Louisiana State Offshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1980's 449 251 260 207 231 1990's 207 207 154 157 168 148 157 130 98 120 2000's 129 145 84 79 61 63 56 65 686 513 2010's 107 51 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease Separation, as of Dec. 31 LA, State Offshore Associated-Dissolved Natural Gas Proved Reserves,

283

ENERGY STAR Update: ENERGY STAR Low Carbon IT Campaign Kicks...  

NLE Websites -- All DOE Office Websites (Extended Search)

Carbon IT Campaign Kicks Off 2013 with Organizations Pledging to Power Manage 360,000 Computers The ENERGY STAR Low Carbon IT (LCIT) Campaign, a nationwide effort to assist and...

284

Low density microcellular carbon foams and method of preparation  

DOE Patents (OSTI)

A low density, open-celled microcellular carbon foam is disclosed which is prepared by dissolving a carbonizable polymer or copolymer in a solvent, pouring the solution into a mold, cooling the solution, removing the solvent, and then carbonizing the polymer or copolymer in a high temperature oven to produce the foam. If desired, an additive can be introduced in order to produce a doped carbon foam, and the foams can be made isotropic by selection of a suitable solvent. The low density, microcellular foams produced by this process are particularly useful in the fabrication of inertial confinement fusion targets, but can also be used as catalysts, absorbents, and electrodes.

Arnold, C. Jr.; Aubert, J.H.; Clough, R.L.; Rand, P.B.; Sylwester, A.P.

1988-06-20T23:59:59.000Z

285

Low density microcellular carbon foams and method of preparation  

SciTech Connect

A low density, open-celled microcellular carbon foam is disclosed which is prepared by dissolving a carbonizable polymer or copolymer in a solvent, pouring the solution into a mold, cooling the solution, removing the solvent, and then carbonizing the polymer or copolymer in a high temperature oven to produce the foam. If desired, an additive can be introduced in order to produce a doped carbon foam, and the foams can be made isotropic by selection of a suitable solvent. The low density, microcellular foams produced by this process are particularly useful in the fabrication of inertial confinement fusion targets, but can also be used as catalysts, absorbents, and electrodes.

Arnold, Jr., Charles (Albuquerque, NM); Aubert, James H. (Albuquerque, NM); Clough, Roger L. (Albuquerque, NM); Rand, Peter B. (Albuquerque, NM); Sylwester, Alan P. (Albuquerque, NM)

1989-01-01T23:59:59.000Z

286

Metal Organic Clathrates for Carbon Dioxide Removal  

removal from coal-fired power plant flue gas streams.  Modified variations of the materials can be used in a variety of other fields as well, ...

287

Worldwide Organic Soil Carbon and Nitrogen Data  

NLE Websites -- All DOE Office Websites (Extended Search)

of soil samples from California. Additional data came from soil surveys of Italy, Greece, Iran, Thailand, Vietnam, various tropical Amazonian areas, and U.S. forests and from...

288

Total Organic Carbon Rejection in Osmotic Distillation.  

E-Print Network (OSTI)

?? The osmotic distillation (OD) system is a spacecraft wastewater recycling system designed to produce potable water from human urine and humidity condensate. The OD… (more)

Shaw, Hali Laraelizabeth

2012-01-01T23:59:59.000Z

289

Soil Organic Carbon in Canadian Soils  

NLE Websites -- All DOE Office Websites (Extended Search)

A. J. VandenBygaart, E. G. Gregorich, and D. A. Angers Agriculture and Agri-Food Canada 960 Carling Avenue Ottawa, Ontario K1A 0C5 Abstract To fulfill commitments under the...

290

NETL: Carbon Storage - Carbon Sequestration Leadership Forum  

NLE Websites -- All DOE Office Websites (Extended Search)

CSLF Carbon Storage Carbon Sequestration Leadership Forum CSLF Logo The Carbon Sequestration Leadership Forum (CSLF) is a voluntary climate initiative of industrially developed and...

291

Intermediate Temperature Carbon - Carbon Composite Structures. CRADA Final Report  

SciTech Connect

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

292

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

293

Organization Chart  

NLE Websites -- All DOE Office Websites (Extended Search)

and Mission Organization Staff - Organization Chart About Us Bob Cottingham, 865-241-0554 Computational Biology and Bioinformatics Meghan Drake 865-241-8288 Michael...

294

Science Organizations  

NLE Websites -- All DOE Office Websites (Extended Search)

Organizations Science Organizations National security depends on science and technology. The United States relies on Los Alamos National Laboratory for the best of both. No place...

295

Low Carbon World | Open Energy Information  

Open Energy Info (EERE)

Low Carbon World Low Carbon World Jump to: navigation, search Tool Summary LAUNCH TOOL Name: LowCarbonWorld Agency/Company /Organization: LowCarbonEconomy Partner: United Nations Environment Programme Sector: Energy, Land Topics: GHG inventory, Background analysis Resource Type: Dataset, Maps Website: www.lowcarboneconomy.com/Low_Carbon_World/Data/Home LowCarbonWorld Screenshot References: LowCarbonWorld[1] Background The idea behind this project was conceived at the 2008 United Nations Conference of Parties (COP14) event in Poznan (Poland). By listening to many speeches by energy ministers from numerous countries in the high level segment of the event, Toddington Harper Managing Director of The Low Carbon Economy Ltd (TLCE) became aware of the depth of valuable information being

296

SOUTHEAST REGIONAL CARBON SEQUESTRATION PARTNERSHIP THE UNITED  

NLE Websites -- All DOE Office Websites (Extended Search)

SOUTHEAST REGIONAL CARBON SEQUESTRATION PARTNERSHIP THE UNITED S T A T E S 2012 ATLAS CARBON UTILIZATION AND STORAGE Southeast Regional Carbon Sequestration Partnership The Southeast Regional Carbon Sequestration Partnership (SECARB), managed by the Southern States Energy Board, represents a 13-state region, including Alabama, Arkansas, Florida, Georgia, Louisiana, Mississippi, North Carolina, South Carolina, Tennessee, eastern Texas, and Virginia and portions of Kentucky and West Virginia. SECARB comprises more than 100 participants representing Federal and state governments, industry, academia, and nonprofit organizations. The primary goal of SECARB is to develop the necessary framework and infrastructure to conduct field tests of carbon storage technologies and to

297

Sandbag Carbon Offset Map | Open Energy Information  

Open Energy Info (EERE)

Sandbag Carbon Offset Map Sandbag Carbon Offset Map Jump to: navigation, search Tool Summary LAUNCH TOOL Name: Sandbag Carbon Offset Map Agency/Company /Organization: Sandbag Sector: Energy, Land Focus Area: Renewable Energy, Biomass, Energy Efficiency, Forestry, Geothermal, Hydrogen, Industry, Solar, Wind Topics: Market analysis Resource Type: Maps, Software/modeling tools User Interface: Website Website: sandbag.org.uk/carbondata/cers Sandbag Carbon Offset Map Screenshot References: Sandbag Carbon Offset Map[1] Thinking about climate change can be a depressing occupation. It's a massive issue and personal actions like switching off lights and unplugging televisions can feel like small contributions. Background "Thinking about climate change can be a depressing occupation. It's a

298

Flux of carbon from 14C-enriched leaf litter throughout a forest soil mesocosm  

SciTech Connect

The role of DOC for the build-up of soil organic carbon pools is still not well known, but it is thought to play a role in the transport of carbon to a greater depth where it becomes more stable. The aim of this study was to elucidate within-year dynamics of carbon transport from litter to the O (Oe and Oa) and A horizons. Mesocosms with constructed soil profiles were used to study dynamics of C transport from 14C-enriched (about 1000 ) leaf litter to the Oe/Oa and A horizons as well as the mineralization of leaf litter. The mesocosms were placed in the field for 17 months during which time fluxes and 14C content of DOC and CO2 were measured. Changes in 14C in leaf litter and bulk soil C pools were also recorded. Significant simultaneous release and immobilization of DOC occurring in both the O and A horizons was hypothesized. Contrary to our hypothesis, DOC released from the labeled Oi horizon was not retained within the Oe/Oa layer. DOC originating in the unlabeled Oe/Oa layer was also released for transport. Extensive retention of DOC occurred in the A horizon. DOC leaching from A horizon consisted of a mix of DOC from different sources, with a main fraction originating in the A horizon and a smaller fraction leached from the overlaying horizons. The C and 14C budget for the litter layer also indicated a surprisingly large amount of carbon with ambient ?14C-signature to be respired from this layer. Data for this site also suggested significant contributions from throughfall to dissolved organic carbon (DOC) transport into and respiration from the litter layer. The results from this study showed that DOC retentionwas low in the O horizon and therefore not important for the O horizon carbon budget. In the A horizon DOC retention was extensive, but annual DOC input was small compared to C stocks and therefore not important for changes in soil C on an annual timescale.

Froberg, Mats J. [Sveriges Lantbruksuniversitet; Hanson, Paul J [ORNL; Trumbore, Susan E. [University of California, Irvine; Swanston, Christopher W. [USFS; Todd Jr, Donald E [ORNL

2009-01-01T23:59:59.000Z

299

Dissolved gaseous mercury behavior in shallow water estuaries  

E-Print Network (OSTI)

The formation of dissolved gaseous mercury (DGM) can be an important pathway for mercury removal from an aquatic environment. DGM evasional fluxes from an aquatic system can account for up to 95% of atmospheric Hg and its deposition pathways. While this makes DGM an important species of mercury to investigate, the difficulty of accurately analyzing DGM has prevented many from studying it. In this study, DGM was measured in two different types of estuarine environments and with two different methods, discrete and continuous analysis. The discrete technique works reasonably well and is reproducible, but it does not allow one to observe rapid changes in DGM concentration due to long analysis times (~2 hr per sample). When used in this study, the discrete sampling technique agreed well with the continuous technique for Offatts Bayou, Galveston, Texas, and Georgiana Slough in the California Bay-Delta region. The average DGM concentration during the March continuous study at Offatts Bayou was 25.3 ± 8.8 pg L-1. This is significantly higher than the average DGM concentration from Georgiana Slough during late March 2006 (9.6 ± 6.6 pg L-1). DGM seemed to correlate best with photosynthetically active radiation (PAR) data in every study, suggesting that the primary control of its formation is solar irradiation. Stronger positive correlations with PAR were seen when DGM data was shifted back one hour, indicating that mercury photoreactions take time to complete. DGM also correlated positively with wind speed in most instances. However, increased wind speed should enhance air to water transfer of elemental mercury, thus one would expect a negative correlation. DGM co-varied negatively with salinity during the continuous studies, suggesting that the DGM pool is reduced in surface waters by chloride mediated oxidation. Three predictive flux models were used in the study to assess the potential for DGM water to air transfer. For both the Georgiana Slough and Offatts Bayou studies, the predicted flux dropped to or below zero after sunset. This study does contribute to the understanding of DGM cycling in aquatic environments as there are few studies that have made continuous DGM measurements in estuarine environments.

Landin, Charles Melchor

2007-12-01T23:59:59.000Z

300

Dissolved gaseous mercury behavior in shallow water estuaries  

E-Print Network (OSTI)

The formation of dissolved gaseous mercury (DGM) can be an important pathway for mercury removal from an aquatic environment. DGM evasional fluxes from an aquatic system can account for up to 95% of atmospheric Hg and its deposition pathways. While this makes DGM an important species of mercury to investigate, the difficulty of accurately analyzing DGM has prevented many from studying it. In this study, DGM was measured in two different types of estuarine environments and with two different methods, discrete and continuous analysis. The discrete technique works reasonably well and is reproducible, but it does not allow one to observe rapid changes in DGM concentration due to long analysis times (~2 hr per sample). When used in this study, the discrete sampling technique agreed well with the continuous technique for Offatts Bayou, Galveston, Texas, and Georgiana Slough in the California Bay-Delta region. The average DGM concentration during the March continuous study at Offatts Bayou was 25.3 + 8.8 pg L-1. This is significantly higher than the average DGM concentration from Georgiana Slough during late March 2006 (9.6 + 6.6 pg L-1). DGM seemed to correlate best with photosynthetically active radiation (PAR) data in every study, suggesting that the primary control of its formation is solar irradiation. Stronger positive correlations with PAR were seen when DGM data was shifted back one hour, indicating that mercury photoreactions take time to complete. DGM also correlated positively with wind speed in most instances. However, increased wind speed should enhance air to water transfer of elemental mercury, thus one would expect a negative correlation. DGM co-varied negatively with salinity during the continuous studies, suggesting that the DGM pool is reduced in surface waters by chloride mediated oxidation. Three predictive flux models were used in the study to assess the potential for DGM water to air transfer. For both the Georgiana Slough and Offatts Bayou studies, the predicted flux dropped to or below zero after sunset. This study does contribute to the understanding of DGM cycling in aquatic environments as there are few studies that have made continuous DGM measurements in estuarine environments.

Landin, Charles Melchor

2007-12-01T23:59:59.000Z

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.


301

Enhancing Low-carbon Development by Greening the Economy: Policy...  

Open Energy Info (EERE)

to: navigation, search Name Enhancing Low-carbon Development by Greening the Economy: Policy Dialogue, Advisory Services, Benchmarking AgencyCompany Organization Deutsche...

302

Enhancing low-carbon development by greening the economy: policy...  

Open Energy Info (EERE)

to: navigation, search Name Enhancing low-carbon development by greening the economy: policy dialogue, advisory services, benchmarking AgencyCompany Organization Deutsche...

303

Numerical Simulation of Carbon and Nitrogen Profiles Produced by ...  

Science Conference Proceedings (OSTI)

In advance of the nitrogen diffusion zone the carbon concentration is as high as 10 at. pct. ... Discovery of Efficient Metal-Organic Frameworks for CO2 Capture.

304

Investigation of the stress induced properties of coke during carbonization.  

E-Print Network (OSTI)

??The large polycyclic aromatic plates within coal tar pitches do not flow freely enough to organize into large anisotropic domains during pyrolytic carbonization. It was… (more)

Maybury, James Joshua.

2007-01-01T23:59:59.000Z

305

Carbon Efficiency, Carbon Reduction Potential, and Economic Development in  

Open Energy Info (EERE)

Carbon Efficiency, Carbon Reduction Potential, and Economic Development in Carbon Efficiency, Carbon Reduction Potential, and Economic Development in the People's Republic of China Jump to: navigation, search Tool Summary LAUNCH TOOL Name: Carbon Efficiency, Carbon Reduction Potential, and Economic Development in the People's Republic of China Agency/Company /Organization: Asian Development Bank Sector: Energy Focus Area: Energy Efficiency, Industry Topics: Low emission development planning, Policies/deployment programs, Background analysis Resource Type: Publications, Case studies/examples Website: www.adb.org/documents/studies/carbon-efficiency-prc/carbon-efficiency- Country: China UN Region: Eastern Asia Coordinates: 35.86166°, 104.195397° Loading map... {"minzoom":false,"mappingservice":"googlemaps3","type":"ROADMAP","zoom":14,"types":["ROADMAP","SATELLITE","HYBRID","TERRAIN"],"geoservice":"google","maxzoom":false,"width":"600px","height":"350px","centre":false,"title":"","label":"","icon":"","visitedicon":"","lines":[],"polygons":[],"circles":[],"rectangles":[],"copycoords":false,"static":false,"wmsoverlay":"","layers":[],"controls":["pan","zoom","type","scale","streetview"],"zoomstyle":"DEFAULT","typestyle":"DEFAULT","autoinfowindows":false,"kml":[],"gkml":[],"fusiontables":[],"resizable":false,"tilt":0,"kmlrezoom":false,"poi":true,"imageoverlays":[],"markercluster":false,"searchmarkers":"","locations":[{"text":"","title":"","link":null,"lat":35.86166,"lon":104.195397,"alt":0,"address":"","icon":"","group":"","inlineLabel":"","visitedicon":""}]}

306

The Carbon Cycle  

NLE Websites -- All DOE Office Websites (Extended Search)

Carbon Cycle Print E-mail U.S. Carbon Cycle Science Program U.S. Carbon Cycle Science Program The U.S. Carbon Cycle Science Program, in consultation with the Carbon Cycle...

307

Simulation of the dissolved oxygen concentration and the pH value at the O2-FET  

Science Conference Proceedings (OSTI)

The O2-FET is a pH ion sensitive field effect transistor (ISFET) modified to measure dissolved oxygen via the acidification from an amperometric dissolved oxygen microsensor. A diffusion based finite elements model which describes the transactions at ... Keywords: ISFET, diffusion, dissolved oxygen, finite elements simulation

J. Wiest; S. Blank; M. Brischwein; H. Grothe; B. Wolf

2008-02-01T23:59:59.000Z

308

Carbon stored in human settlements: the conterminous  

E-Print Network (OSTI)

Urban areas are home to more than half of the world’s people, responsible for 470 % of anthropogenic release of carbon dioxide and 76 % of wood used for industrial purposes. By 2050 the proportion of the urban population is expected to increase to 70 % worldwide. Despite fast rates of change and potential value for mitigation of carbon dioxide emissions, the organic carbon storage in human settlements has not been well quantified. Here, we show that human settlements can store as much carbon per unit area (23–42 kg C m 2 urban areas and 7–16 kg C m 2 exurban areas) as tropical forests, which have the highest carbon density of natural ecosystems (4–25 kg C m 2). By the year 2000 carbon storage attributed to human settlements of the conterminous United States was 18 Pg of carbon or 10 % of its total land carbon storage. Sixty-four percent of this carbon was attributed to soil, 20 % to vegetation, 11 % to landfills, and 5 % to buildings. To offset rising urban emissions of carbon, regional and national governments should consider how to protect or even to increase carbon storage of human-dominated landscapes. Rigorous studies addressing carbon budgets of human settlements and vulnerability of their carbon storage are needed.

unknown authors

2009-01-01T23:59:59.000Z

309

Carbon Sequestration  

NLE Websites -- All DOE Office Websites (Extended Search)

David a. Lang David a. Lang Project Manager National Energy Technology Laboratory 626 Cochrans Mill Road P.O. Box 10940 Pittsburgh, PA 15236 412-386-4881 david.lang@netl.doe.gov andrew chizmeshya Arizona State University Center for Solid State Science Tempe, AZ 85287-1704 480-965-6072 chizmesh@asu.edu A Novel ApproAch to MiNerAl cArboNAtioN: eNhANciNg cArboNAtioN While AvoidiNg MiNerAl pretreAtMeNt process cost Background Carbonation of the widely occurring minerals of the olivine group, such as forsterite (Mg 2 SiO 4 ), is a potential large-scale sequestration process that converts CO 2 into the environmentally benign mineral magnesite (MgCO 3 ). Because the process is exothermic, it inherently offers low-cost potential. Enhancing carbonation reactivity is the key to economic viability. Previous

310

Large Magnetization at Carbon Surfaces  

NLE Websites -- All DOE Office Websites (Extended Search)

Large Magnetization at Carbon 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 element. Now, another use has been found: magnets. One would not expect pure carbon to be magnetic, but for more than ten years scientists have suspected that carbon can be made to be magnetic by doping it with nonmagnetic materials, changing its order ever so slightly. Years ago, the first x-ray images obtained using the scanning transmission x-ray microscope at ALS Beamline 11.0.2 provided valuable insight into how proton irradiation can cause carbon to transform into a ferromagnetic material. Now, researchers are using x-ray spectroscopy at ALS Beamline 4.0.2 to study the magnetism of proton-irradiated graphite surfaces in order to understand the effects of hydrogen (i.e. protons) on the electronic structure of carbon. In studying the properties of electrons responsible for magnetic order in graphite, researchers found that a very large magnetic moment is essentially switched on when hydrogen atoms are incorporated at the surface of graphite.

311

New Mexico - West Associated-Dissolved Natural Gas, Wet After Lease  

Gasoline and Diesel Fuel Update (EIA)

West Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) West Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) New Mexico - West Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 151 1980's 156 150 146 180 194 181 214 213 259 178 1990's 184 156 127 107 97 119 108 106 98 92 2000's 115 99 103 89 90 98 82 87 86 82 2010's 105 143 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease

312

Utah Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved  

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Utah Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 367 1980's 414 335 325 360 341 391 410 471 475 442 1990's 455 469 309 289 286 277 301 310 209 321 2000's 348 303 359 299 290 308 317 368 321 601 2010's 631 909 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease Separation, as of Dec. 31

313

Kansas Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved  

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Kansas Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 167 1980's 185 139 112 132 110 115 132 115 103 101 1990's 114 115 94 93 75 67 82 51 60 52 2000's 40 105 66 85 80 83 82 83 85 83 2010's 79 127 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease Separation, as of Dec. 31

314

North Dakota Associated-Dissolved Natural Gas, Wet After Lease Separation,  

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) North Dakota Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 201 1980's 239 253 248 257 267 331 293 276 266 313 1990's 334 243 266 274 275 263 255 257 261 250 2000's 264 270 315 316 320 343 357 417 484 1,070 2010's 1,717 2,511 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease

315

Ohio Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved  

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Ohio Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 1,047 1980's 1,417 800 984 1,635 1,178 938 898 594 480 589 1990's 371 376 381 343 315 355 399 391 342 402 2000's 469 340 346 304 208 184 174 101 99 97 2010's 90 74 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease Separation, as of Dec. 31

316

Texas - RRC District 4 Onshore Associated-Dissolved Natural Gas, Wet After  

Gasoline and Diesel Fuel Update (EIA)

4 Onshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) 4 Onshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Texas - RRC District 4 Onshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 1,416 1980's 1,292 1,005 890 765 702 684 596 451 393 371 1990's 301 243 228 215 191 209 246 368 394 182 2000's 176 140 150 136 165 148 110 117 127 96 2010's 91 61 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease

317

California State Offshore Associated-Dissolved Natural Gas, Wet After Lease  

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) California State Offshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 226 1980's 160 244 232 221 206 1990's 188 55 59 63 59 56 47 54 39 58 2000's 86 80 85 76 85 89 85 79 54 53 2010's 63 79 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease Separation, as of Dec. 31

318

Texas - RRC District 1 Associated-Dissolved Natural Gas, Wet After Lease  

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

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Texas - RRC District 1 Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 209 1980's 172 180 216 175 170 260 241 205 204 251 1990's 333 401 361 191 151 248 446 68 51 67 2000's 69 43 47 48 45 57 61 72 60 67 2010's 267 900 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease

319

Gulf of Mexico Federal Offshore - Texas Associated-Dissolved Natural Gas,  

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

Texas Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Texas Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Gulf of Mexico Federal Offshore - Texas Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1980's 474 320 541 522 532 494 1990's 446 407 691 574 679 891 794 1,228 1,224 1,383 2000's 1,395 1,406 1,267 1,119 886 547 378 377 465 629 2010's 689 539 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease

320

West Virginia Associated-Dissolved Natural Gas, Wet After Lease Separation,  

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) West Virginia Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 76 1980's 122 63 83 86 73 73 65 150 141 98 1990's 86 159 198 190 133 74 71 59 43 88 2000's 98 48 21 23 20 19 16 16 23 24 2010's 29 52 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease Separation, as of Dec. 31

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

Texas - RRC District 2 Onshore Associated-Dissolved Natural Gas, Wet After  

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

2 Onshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) 2 Onshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Texas - RRC District 2 Onshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 955 1980's 921 806 780 747 661 570 517 512 428 430 1990's 407 352 308 288 299 245 252 235 204 202 2000's 115 65 70 81 76 109 118 137 72 72 2010's 134 924 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease

322

Calibration, Response, and Hysteresis in Deep-Sea Dissolved Oxygen Measurements  

Science Conference Proceedings (OSTI)

Accurately measuring the dissolved oxygen concentration in the ocean has been the subject of considerable research. Traditionally, the calibration and correction of profiling oxygen measurements has centered on static, steady-state errors, ...

Bradley Edwards; David Murphy; Carol Janzen; Nordeen Larson

2010-05-01T23:59:59.000Z

323

Table 13: Associated-dissolved natural gas proved reserves, reserves changes, an  

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

: Associated-dissolved natural gas proved reserves, reserves changes, and production, wet after lease separation, 2011" : Associated-dissolved natural gas proved reserves, reserves changes, and production, wet after lease separation, 2011" "billion cubic feet" ,,"Changes in Reserves During 2011" ,"Published",,,,,,,,"New Reservoir" ,"Proved",,"Revision","Revision",,,,"New Field","Discoveries","Estimated","Proved" ,"Reserves","Adjustments","Increases","Decreases","Sales","Acquisitions","Extensions","Discoveries","in Old Fields","Production","Reserves" "State and Subdivision",40543,"(+,-)","(+)","(-)","(-)","(+)","(+)","(+)","(+)","(-)",40908

324

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

DOE Green Energy (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

325

Organization | Department of Energy  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

About Us Organization Organization Leadership Organization History Careers Contact Us Organization...

326

PREDICTION OF TOTAL DISSOLVED GAS EXCHANGE AT HYDROPOWER DAMS  

DOE Green Energy (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

327

Allied Carbon Credit GmbH | Open Energy Information  

Open Energy Info (EERE)

Carbon Credit GmbH Carbon Credit GmbH Jump to: navigation, search Name Allied Carbon Credit GmbH Place Hessen, Germany Sector Carbon Product Frankfurt-based carbon advisory and consultancy firm. References Allied Carbon Credit GmbH[1] LinkedIn Connections CrunchBase Profile No CrunchBase profile. Create one now! This article is a stub. You can help OpenEI by expanding it. Allied Carbon Credit GmbH is a company located in Hessen, Germany . References ↑ "Allied Carbon Credit GmbH" Retrieved from "http://en.openei.org/w/index.php?title=Allied_Carbon_Credit_GmbH&oldid=342020" Categories: Clean Energy Organizations Companies Organizations Stubs What links here Related changes Special pages Printable version Permanent link Browse properties 429 Throttled (bot load)

328

Organic aerogel microspheres  

Science Conference Proceedings (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

329

NETL: Carbon Storage - West Coast Regional Carbon Sequestration Partnership  

NLE Websites -- All DOE Office Websites (Extended Search)

WESTCARB WESTCARB Carbon Storage West Coast Regional Carbon Sequestration Partnership MORE INFO Additional information related to ongoing WESTCARB efforts can be found on their website. The West Coast Regional Carbon Sequestration Partnership (WESTCARB) is led by the California Energy Commission and represents a coalition of more than 90 organizations from state and provincial resource management and environmental protection agencies; national laboratories and research institutions; colleges and universities; conservation non-profits; oil and gas companies; power companies; pipeline companies; trade associations; vendors and service firms; and consultants. The partners are engaged in several aspects of WESTCARB projects and contribute to the efforts to deploy carbon storage projects on the west coast of North America. WESTCARB

330

NETL: Carbon Storage - Southwest Regional Partnership on Carbon  

NLE Websites -- All DOE Office Websites (Extended Search)

Southwest Regional Partnership on Carbon Sequestration Southwest Regional Partnership on Carbon Sequestration MORE INFO Additional information related to ongoing SWP efforts can be found on their website. The Southwest Regional Partnership on Carbon Sequestration (SWP) is led by the New Mexico Institute of Mining and Technology and represents a coalition composed of a diverse group of experts in geology, engineering, economics, public policy, and outreach. The 50 SWP partners represent state and federal agencies, universities, electric utilities, non-governmental organizations, coal, oil and gas companies, and the Navajo Nation. The partners are engaged in several aspects of SWP projects and contribute to the efforts to deploy carbon capture and storage (CCS) projects in the southwestern region of the United States. SWP encompasses Arizona,

331

CUFR Tree Carbon Calculator | Open Energy Information  

Open Energy Info (EERE)

CUFR Tree Carbon Calculator CUFR Tree Carbon Calculator Jump to: navigation, search Tool Summary LAUNCH TOOL Name: CUFR Tree Carbon Calculator Agency/Company /Organization: United States Forest Service Sector: Climate, Land Focus Area: Forestry Phase: Determine Baseline, Evaluate Options Topics: GHG inventory, Resource assessment Resource Type: Software/modeling tools User Interface: Desktop Application Website: www.fs.fed.us/ccrc/topics/urban-forests/ctcc/ Cost: Free Language: English References: CUFR Tree Carbon Calculator[1] Overview "The CUFR Tree Carbon Calculator is the only tool approved by the Climate Action Reserve's Urban Forest Project Protocol for quantifying carbon dioxide sequestration from GHG tree planting projects. The CTCC is programmed in an Excel spreadsheet and provides carbon-related information

332

Gas adsorption on metal-organic frameworks  

SciTech Connect

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

333

Modern Records of Carbon and Oxygen Isotopes in Atmospheric Carbon...  

NLE Websites -- All DOE Office Websites (Extended Search)

Modern Records of Carbon and Oxygen Isotopes in Atmospheric Carbon Dioxide and Carbon-13 in Methane Modern Records of Carbon and Oxygen Isotopes in Atmospheric Carbon Dioxide and...

334

NIST Organization  

Science Conference Proceedings (OSTI)

... What We Do; Organization Chart; Budget Information; Office of the Director; Laboratories & Major Programs; Locations; Staff Directory; Working With ...

2013-02-19T23:59:59.000Z

335

Symposium Organizer  

Science Conference Proceedings (OSTI)

Volunteer Training Module. March 2013. 1. Your Professional Partner for Career Advancement. Symposium Organizer. Online Training Module. March 2013 ...

336

Carbonate Mineralization of Volcanic Province Basalts  

Science Conference Proceedings (OSTI)

Flood basalts are receiving increasing attention as possible host formations for geologic sequestration of anthropogenic CO2, with studies underway in the United States, India, Iceland, and Canada. As an extension of our previous experiments with Columbia River basalt, basalts from the eastern United States, India, and South Africa were reacted with aqueous dissolved CO2 and aqueous dissolved CO2-H2S mixtures under supercritical CO2 (scCO2) conditions to study the geochemical reactions resulting from injection of CO2 in such formations. The results of these studies are consistent with cation release behavior measured in our previous experiments (in press) for basalt samples tested in single pass flow through dissolution experiments under dilute solution and mildly acidic conditions. Despite the basalt samples having similar bulk chemistry, mineralogy and apparent dissolution kinetics, long-term static experiments show significant differences in rates of mineralization as well as compositions and morphologies of precipitates that form when the basalts are reacted with CO2-saturated water. For example, basalt from the Newark Basin in the United States was by far the most reactive of any basalt tested to date. Carbonate reaction products for the Newark Basin basalt were globular in form and contained significantly more Fe than the secondary carbonates that precipitated on the other basalt samples. In comparison, the post-reacted samples associated with the Columbia River basalts from the United States contained calcite grains with classic dogtooth spar morphology and trace cation substitution (Mg and Mn). Carbonation of the other basalts produced precipitates with compositions that varied chemically throughout the entire testing period. Examination of polished cross sections of the reacted grains by scanning electron microscopy and energy dispersive x-ray spectroscopy show precipitate overgrowths with varying chemical compositions. Compositional differences in the precipitates suggest changes in fluid chemistry unique to the dissolution behavior of each basalt sample reacted with CO2-saturated water. The Karoo basalt from South Africa appeared the least reactive, with very limited mineralization occurring during the testing with CO2-saturated water. The relative reactivity of different basalt samples were unexpectedly different in the experiments conducted using aqueous dissolved CO2-H2S mixtures versus those reacted with aqueous dissolved CO2 mixtures. For example, the Karoo basalt was highly reactive in the presence of aqueous dissolved CO2-H2S, as evident by small nodules of carbonate coating the basalt grains after 181 days of testing. However the most reactive basalt in CO2-H2O, Newark Basin, formed limited amounts of carbonate precipitates in the presence of aqueous dissolved CO2-H2S mixture. Basalt reactivity in CO2-H2O mixtures appears to be controlled by the composition of the glassy mesostasis, which is the most reactive component in the basalt rock. With the addition of H2S to the CO2-H2O system, basalt reactivity appears to be controlled by precipitation of coatings of insoluble Fe sulfides.

Schaef, Herbert T.; McGrail, B. Peter; Owen, Antionette T.

2010-03-31T23:59:59.000Z

337

Method for making carbon films  

DOE Patents (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

338

Method for making carbon films  

DOE Patents (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 (.apprxeq.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.degree. 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.degree. 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.degree. C. for between 1-6 hours.

Tan, Ming X. (Livermore, CA)

1999-01-01T23:59:59.000Z

339

Method of stripping metals from organic solvents  

DOE Patents (OSTI)

A new method to strip metals from organic solvents in a manner that allows for the recycle of the stripping agent. The method utilizes carbonate solutions of organic amines with complexants, in low concentrations, to strip metals from organic solvents. The method allows for the distillation and reuse of organic amines. The concentrated metal/complexant fraction from distillation is more amenable to immobilization than solutions resulting from current practice.

Todd, Terry A. (Aberdeen, ID); Law, Jack D. (Pocatello, ID); Herbst, R. Scott (Idaho Falls, ID); Romanovskiy, Valeriy N. (St. Petersburg, RU); Smirnov, Igor V. (St.-Petersburg, RU); Babain, Vasily A. (St-Petersburg, RU); Esimantovski, Vyatcheslav M. (St-Petersburg, RU)

2009-02-24T23:59:59.000Z

340

Carbon supercapacitors  

SciTech Connect

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

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

Carbon particles  

DOE Patents (OSTI)

A method and apparatus whereby small carbon particles are made by pyrolysis of a mixture of acetylene carried in argon. The mixture is injected through a nozzle into a heated tube. A small amount of air is added to the mixture. In order to prevent carbon build-up at the nozzle, the nozzle tip is externally cooled. The tube is also elongated sufficiently to assure efficient pyrolysis at the desired flow rates. A key feature of the method is that the acetylene and argon, for example, are premixed in a dilute ratio, and such mixture is injected while cool to minimize the agglomeration of the particles, which produces carbon particles with desired optical properties for use as a solar radiant heat absorber.

Hunt, Arlon J. (Oakland, CA)

1984-01-01T23:59:59.000Z

342

SEPARATION OF INORGANIC SALTS FROM ORGANIC SOLUTIONS  

DOE Patents (OSTI)

A process is described for recovering the nitrates of uranium and plutonium from solution in oxygen-containing organic solvents such as ketones or ethers. The solution of such salts dissolved in an oxygen-containing organic compound is contacted with an ion exchange resin whereby sorption of the entire salt on the resin takes place and then the salt-depleted liquid and the resin are separated from each other. The reaction seems to be based on an anion formation of the entire salt by complexing with the anion of the resin. Strong base or quaternary ammonium type resins can be used successfully in this process.

Katzin, L.I.; Sullivan, J.C.

1958-06-24T23:59:59.000Z

343

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

344

Large Magnetization at Carbon Surfaces  

NLE Websites -- All DOE Office Websites (Extended Search)

Large Magnetization at Carbon Surfaces Print Large Magnetization at Carbon Surfaces Print From organic matter to pencil lead, carbon is a versatile element. Now, another use has been found: magnets. One would not expect pure carbon to be magnetic, but for more than ten years scientists have suspected that carbon can be made to be magnetic by doping it with nonmagnetic materials, changing its order ever so slightly. Years ago, the first x-ray images obtained using the scanning transmission x-ray microscope at ALS Beamline 11.0.2 provided valuable insight into how proton irradiation can cause carbon to transform into a ferromagnetic material. Now, researchers are using x-ray spectroscopy at ALS Beamline 4.0.2 to study the magnetism of proton-irradiated graphite surfaces in order to understand the effects of hydrogen (i.e. protons) on the electronic structure of carbon. In studying the properties of electrons responsible for magnetic order in graphite, researchers found that a very large magnetic moment is essentially switched on when hydrogen atoms are incorporated at the surface of graphite.

345

Large Magnetization at Carbon Surfaces  

NLE Websites -- All DOE Office Websites (Extended Search)

Large Magnetization at Carbon Surfaces Print Large Magnetization at Carbon Surfaces Print From organic matter to pencil lead, carbon is a versatile element. Now, another use has been found: magnets. One would not expect pure carbon to be magnetic, but for more than ten years scientists have suspected that carbon can be made to be magnetic by doping it with nonmagnetic materials, changing its order ever so slightly. Years ago, the first x-ray images obtained using the scanning transmission x-ray microscope at ALS Beamline 11.0.2 provided valuable insight into how proton irradiation can cause carbon to transform into a ferromagnetic material. Now, researchers are using x-ray spectroscopy at ALS Beamline 4.0.2 to study the magnetism of proton-irradiated graphite surfaces in order to understand the effects of hydrogen (i.e. protons) on the electronic structure of carbon. In studying the properties of electrons responsible for magnetic order in graphite, researchers found that a very large magnetic moment is essentially switched on when hydrogen atoms are incorporated at the surface of graphite.

346

Large Magnetization at Carbon Surfaces  

NLE Websites -- All DOE Office Websites (Extended Search)

Large Magnetization at Carbon Surfaces Print Large Magnetization at Carbon Surfaces Print From organic matter to pencil lead, carbon is a versatile element. Now, another use has been found: magnets. One would not expect pure carbon to be magnetic, but for more than ten years scientists have suspected that carbon can be made to be magnetic by doping it with nonmagnetic materials, changing its order ever so slightly. Years ago, the first x-ray images obtained using the scanning transmission x-ray microscope at ALS Beamline 11.0.2 provided valuable insight into how proton irradiation can cause carbon to transform into a ferromagnetic material. Now, researchers are using x-ray spectroscopy at ALS Beamline 4.0.2 to study the magnetism of proton-irradiated graphite surfaces in order to understand the effects of hydrogen (i.e. protons) on the electronic structure of carbon. In studying the properties of electrons responsible for magnetic order in graphite, researchers found that a very large magnetic moment is essentially switched on when hydrogen atoms are incorporated at the surface of graphite.

347

Large Magnetization at Carbon Surfaces  

NLE Websites -- All DOE Office Websites (Extended Search)

Large Magnetization at Carbon Surfaces Print Large Magnetization at Carbon Surfaces Print From organic matter to pencil lead, carbon is a versatile element. Now, another use has been found: magnets. One would not expect pure carbon to be magnetic, but for more than ten years scientists have suspected that carbon can be made to be magnetic by doping it with nonmagnetic materials, changing its order ever so slightly. Years ago, the first x-ray images obtained using the scanning transmission x-ray microscope at ALS Beamline 11.0.2 provided valuable insight into how proton irradiation can cause carbon to transform into a ferromagnetic material. Now, researchers are using x-ray spectroscopy at ALS Beamline 4.0.2 to study the magnetism of proton-irradiated graphite surfaces in order to understand the effects of hydrogen (i.e. protons) on the electronic structure of carbon. In studying the properties of electrons responsible for magnetic order in graphite, researchers found that a very large magnetic moment is essentially switched on when hydrogen atoms are incorporated at the surface of graphite.

348

Separation of organic ion exchange resins from sludge -- engineering study  

SciTech Connect

This engineering study evaluates the use of physical separation technologies to separate organic ion exchange resin from KE Basin sludge prior to nitric acid dissolution. This separation is necessitate to prevent nitration of the organics in the acid dissolver. The technologies under consideration are: screening, sedimentation, elutriation. The recommended approach is to first screen the Sludge and resin 300 microns then subject the 300 microns plus material to elutriation.

Duncan, J.B.

1998-08-25T23:59:59.000Z

349

Low Carbon Economy Index 2010 | Open Energy Information  

Open Energy Info (EERE)

Low Carbon Economy Index 2010 Low Carbon Economy Index 2010 Jump to: navigation, search Tool Summary Name: Low Carbon Economy Index 2010 Agency/Company /Organization: PricewaterhouseCoopers Sector: Energy, Land Topics: Co-benefits assessment, Low emission development planning Resource Type: Publications Website: www.pwc.co.uk/ Low Carbon Economy Index 2010 Screenshot References: Low Carbon Economy Index 2010[1] "PwC re-examines the progress of the G20 economies against the Low Carbon Achievement and Low Carbon Challenge Index. This post- Copenhagen report provides an update on the progress over 2009." Low Carbon Economy Index 2010 References ↑ "Low Carbon Economy Index 2010" Retrieved from "http://en.openei.org/w/index.php?title=Low_Carbon_Economy_Index_2010&oldid=3841

350

Forest Carbon Partnership Facility | Open Energy Information  

Open Energy Info (EERE)

Forest Carbon Partnership Facility Forest Carbon Partnership Facility Jump to: navigation, search Logo: Forest Carbon Partnership Facility Name Forest Carbon Partnership Facility Agency/Company /Organization World Bank Sector Land Focus Area Forestry Topics Co-benefits assessment, Finance Resource Type Lessons learned/best practices, Training materials Website http://www.forestcarbonpartner Country Argentina, Bolivia, Cambodia, Cameroon, Central African Republic, Chile, Colombia, Costa Rica, Democratic Republic of Congo, El Salvador, Equatorial Guinea, Ethiopia, Gabon, Ghana, Guatemala, Guyana, Honduras, Indonesia, Kenya, Laos, Laos, Liberia, Madagascar, Mexico, Moldova, Mozambique, Nepal, Nicaragua, Panama, Papua New Guinea, Paraguay, Peru, Republic of the Congo, Suriname, Tanzania, Thailand, Uganda, Vanuatu, Vietnam

351

Oxidation and methylation of dissolved elemental mercury by anaerobic bacteria  

Science Conference Proceedings (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

352

Preparation of Carbon Nanotube-Composite  

E-Print Network (OSTI)

A composite is made up of two distinct materials and the resulted properties are different from the individual precursors. Composite combines a huge or bulkier element called matrix and reinforcement called filler or fiber. Fiber is added in the matrix to increase the stiffness of the matrix and enhance or alter its physical properties. Since silk has high levels of toughness, strength and multifunctional nature, we decided to use bombyx mori as a matrix. Because of the superior mechanical properties, i.e., high tensile moduli, and strength of carbon nanotube, we chose carbon nanotube as a reinforcement fiber to enhance the mechanical properties of resulting composite. The main issue encountered while preparing composite was to fully disperse individual nanotubes in the matrices, because nanotubes tend to form clusters and bundles. Hence, we used ionic liquids to dissolve the cocoon, and processed homogenization of FCNT with silk by sonication, stirring. For testing, different weight percentages of functionalized carbon nanotube were used as a filler to make the silk composite, and nanoindentation and tensile tester tested the samples. The composite of various concentrations did not show the expected result of increasing mechanical properties with decreased carbon nanotube concentration. Hence, it was concluded that a different method to functionalize carbon nanotube should be implemented.

Sharma, Sundeep

2011-05-01T23:59:59.000Z

353

Major role of marine vegetation on the oceanic carbon cycle  

E-Print Network (OSTI)

Abstract. The carbon burial in vegetated sediments, ignored in past assessments of carbon burial in the ocean, was evaluated using a bottom-up approach derived from upscaling a compilation of published individual estimates of carbon burial in vegetated habitats (seagrass meadows, salt marshes and mangrove forests) to the global level and a top-down approach derived from considerations of global sediment balance and a compilation of the organic carbon content of vegeatated sediments. Up-scaling of individual burial estimates values yielded a total carbon burial in vegetated habitats of 111 Tmol C y ?1. The total burial in unvegetated sediments was estimated to be 126 Tg C y ?1, resulting in a bottom-up estimate of total burial in the ocean of about 244 Tg C y ?1, two-fold higher than estimates of oceanic carbon burial that presently enter global carbon budgets. The organic carbon

C. M. Duarte; J. J. Middelburg; N. Caraco

2005-01-01T23:59:59.000Z

354

Transport Models for Radioactive Carbon Dioxide at RWMC  

SciTech Connect

Radioactive carbon dioxide (formed by oxidation of carbon-14) is a highly mobile, radioactive contaminant released from solid wastes buried at the Subsurface Disposal Area (SDA) at the Radioactive Waste Management Complex (RWMC) at the Idaho National Engineering and Environmental Laboratory (INEEL). Radioactive CO2 is chemically active in the environment, volatile, water soluble, and subject to adsorption on solids. For this reason, its fate must be understood and controlled to meet radiological requirements (protection of the atmosphere, aquifer, vadose zones, plants and animals). In the present work, the migration of carbon-14 as dissolved bicarbonate was studied using miscible displacement experiments in water-saturated columns containing sediments from RWMC. Dissolved carbon-14 was retarded relative to the movement of water by a factor of about 3.6, which translates to a partition coefficient (Kd) of 0.8 ml/g. Two different adsorption sites were identified, with one site possibly having a nonlinear adsorption isotherm. A conservative tracer gas, sulfur hexafluoride, was used to measure the tortuosity of sedimentary material for gaseous diffusion. The tortuosity of the RWMC sediment (Spreading Area B sediment) was determined to be 3.2, which is slightly greater than predicted by the commonly used Millington-Quirk equation. In terms of affecting the migration of carbon-14 to the aquifer, the relative importance of the parameters studied is: (1) natural moisture content of the sediments, (2) sediment tortuosity to gas-phase diffusion, and (3) adsorption onto solid phases.

Hull, Laurence Charles; Hohorst, Frederick August

2001-12-01T23:59:59.000Z

355

Carbon | Open Energy Information  

Open Energy Info (EERE)

Carbon Sector Retrieved from "http:en.openei.orgwindex.php?titleCarbon&oldid271960" Categories: Articles with outstanding TODO tasks...

356

Landscape level differences in soil carbon and nitrogen: implications for soil carbon sequestration  

SciTech Connect

The objective of this research was to understand how land cover and topography act, independently or together, as determinants of soil carbon and nitrogen storage over a complex terrain. Such information could help to direct land management for the purpose of carbon sequestration. Soils were sampled under different land covers and at different topographic positions on the mostly forested 14,000 ha Oak Ridge Reservation in Tennessee, USA. Most of the soil carbon stock, to a 40-cm soil depth, was found to reside in the surface 20 cm of mineral soil. Surface soil carbon and nitrogen stocks were partitioned into particulate ({ge}53 {micro}m) and mineral-associated organic matter (<53 {micro}m). Generally, soils under pasture had greater nitrogen availability, greater carbon and nitrogen stocks, and lower C:N ratios than soils under transitional vegetation and forests. The effects of topography were usually secondary to those of land cover. Because of greater soil carbon stocks, and greater allocation of soil carbon to mineral-associated organic matter (a long-term pool), we conclude that soil carbon sequestration, but not necessarily total ecosystem carbon storage, is greater under pastures than under forests. The implications of landscape-level variation in soil carbon and nitrogen for carbon sequestration are discussed at several different levels: (1) nitrogen limitations to soil carbon storage; (2) controls on soil carbon turnover as a result of litter chemistry and soil carbon partitioning; (3) residual effects of past land use history; and (4) statistical limitations to the quantification of soil carbon stocks.

Garten Jr, Charles T [ORNL; Ashwood, Tom L [ORNL

2002-12-01T23:59:59.000Z

357

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

SciTech Connect

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

358

Organization Chart  

NLE Websites -- All DOE Office Websites (Extended Search)

spacer spacer spacer About DOE Organization News Contact Us Search Search Go spacer U.S. Department of Energy header image Science & Technology Energy Sources Energy Efficiency...

359

Variations in dissolved gas compositions of reservoir fluids from the Coso  

Open Energy Info (EERE)

Variations in dissolved gas compositions of reservoir fluids from the Coso Variations in dissolved gas compositions of reservoir fluids from the Coso geothermal field Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Conference Proceedings: Variations in dissolved gas compositions of reservoir fluids from the Coso geothermal field Details Activities (1) Areas (1) Regions (0) Abstract: Gas concentrations and ratios in 110 analyses of geothermal fluids from 47 wells in the Coso geothermal system illustrate the complexity of this two-phase reservoir in its natural state. Two geographically distinct regions of single-phase (liquid) reservoir are present and possess distinctive gas and liquid compositions. Relationships in soluble and insoluble gases preclude derivation of these waters from a common parent by boiling or condensation alone. These two regions may

360

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

Science Conference Proceedings (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

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

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

362

Carbon Additionality: Discussion Paper  

E-Print Network (OSTI)

Carbon Additionality: A review Discussion Paper Gregory Valatin November 2009 Forest Research. Voluntary Carbon Standards American Carbon Registry Forest Carbon Project Standard (ACRFCPS) 27 CarbonFix Standard (CFS) 28 Climate, Community and Biodiversity Standard (CCBS) 28 Forest Carbon Standard (FCS) 28

363

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

Science Conference Proceedings (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

364

Low Carbon Development: Planning & Modelling Course | Open Energy  

Open Energy Info (EERE)

Low Carbon Development: Planning & Modelling Course Low Carbon Development: Planning & Modelling Course Jump to: navigation, search Tool Summary LAUNCH TOOL Name: Low Carbon Development: Planning & Modelling Course Agency/Company /Organization: World Bank Sector: Climate Focus Area: Renewable Energy, Economic Development, People and Policy Topics: Low emission development planning, Pathways analysis, Resource assessment Resource Type: Training materials, Workshop Website: einstitute.worldbank.org/ei/course/low-carbon-development Cost: Paid References: Low Carbon Development: Planning & Modelling[1] Program Overview This course has the following modules - (i) Introduction to Low Carbon Development Planning; (ii) Overview for Policymakers; (iii) Power; (iv) Household; (v) Transport - which introduce you to climate change

365

On the Importance of Organic Oxygen for Understanding OrganicAerosol Particles  

SciTech Connect

This study shows how aerosol organic oxygen data could provide new information about organic aerosol mass, aqueous solubility of organic aerosols, formation of secondary organic aerosol (SOA) and the relative contributions of anthropogenic and biogenic sources. For more than two decades atmospheric aerosol organic mass (OM) concentration has been estimated by multiplying the measured carbon content by an assumed (OM)-to-organic carbon (OC) factor, usually 1.4. However, this factor can vary from 1.0 to 2.5 depending on location. This large uncertainty about aerosol organic mass limits our understanding of the influence of organic aerosol on climate, visibility and health. New examination of organic aerosol speciation data shows that the oxygen content is responsible for the observed range in the OM-to-OC factor. When organic oxygen content is excluded, the ratio of non-oxygen organic mass to carbon mass varies very little across different environments (1.12 to 1.14). The non-oxygen-OM-to-OC factor for all studied sites (urban and non-urban) averaged 1.13. The uncertainty becomes an order of magnitude smaller than the uncertainty in the best current estimates of organic mass to organic carbon ratios (1.6 {+-} 0.2 for urban and 2.1 {+-} 0.2 for non-urban areas). This analysis suggests that, when aerosol organic oxygen data become available, organic aerosol mass can be quite accurately estimated using just OC and organic oxygen (OO) without the need to know whether the aerosol is fresh or aged. In addition, aerosol organic oxygen data will aid prediction of water solubility since compounds with OO-to-OC higher than 0.4 have water solubilities higher than 1 g per 100 g water.

Pang, Y.; Turpin, B.J.; Gundel, L.A.

2005-04-01T23:59:59.000Z

366

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

SciTech Connect

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

2010-07-01T23:59:59.000Z

367

Forest Carbon Index | Open Energy Information  

Open Energy Info (EERE)

Forest Carbon Index Forest Carbon Index Jump to: navigation, search Tool Summary LAUNCH TOOL Name: Forest Carbon Index Agency/Company /Organization: Resources for the Future Partner: United Nations Foundation Sector: Land Focus Area: Forestry Topics: Finance, GHG inventory, Market analysis Resource Type: Maps, Software/modeling tools User Interface: Website Website: www.forestcarbonindex.org/ Web Application Link: www.forestcarbonindex.org/maps.html Cost: Free References: Forest Carbon Index [1] The Forest Carbon Index (FCI) compiles and displays global data relating to biological, economic, governance, investment, and market readiness conditions for every forest and country in the world, revealing the best places and countries for forest carbon investments. Please use this site to

368

Carbon Sequestration  

NLE Websites -- All DOE Office Websites (Extended Search)

Technology Technology Laboratory 626 Cochrans Mill Road P.O. Box 10940 Pittsburgh, PA 15236-0940 412-386-4966 jose.figueroa@netl.doe.gov Kevin o'Brien Principal Investigator SRI International Materials Research Laboratory 333 Ravenswood Avenue Menlo Park, AK 94025 650-859-3528 kevin.obrien@sri.com Fabrication and Scale-Up oF polybenzimidazole - baSed membrane SyStem For pre - combUStion captUre oF carbon dioxide Background In order to effectively sequester carbon dioxide (CO 2 ) from a gasification plant, there must be an economically viable method for removing the CO 2 from other gases. While CO 2 separation technologies currently exist, their effectiveness is limited. Amine-based separation technologies work only at low temperatures, while pressure-swing absorption and cryogenic distillation consume significantly

369

Carbon Sequestration  

NLE Websites -- All DOE Office Websites (Extended Search)

andrea Mcnemar andrea Mcnemar National Energy Technology Laboratory 3610 Collins Ferry Road P.O. Box 880 Morgantown, WV 26507-0880 304-285-2024 andrea.mcnemar@netl.doe.gov Gregory J. Elbring Principal Investigator Sandia National Laboratory P.O. Box 5800 Albuquerque, NM 87185 505-844-4904 gjelbri@sandia.gov GeoloGic SequeStration of carbon DioxiDe in a DepleteD oil reServoir: a comprehenSive moDelinG anD Site monitorinG project Background The use of carbon dioxide (CO 2 ) to enhance oil recovery (EOR) is a familiar and frequently used technique in the United States. The oil and gas industry has significant experience with well drilling and injecting CO 2 into oil-bearing formations to enhance production. While using similar techniques as in oil production, this sequestration field

370

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

Science Conference Proceedings (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

371

NETL: Carbon Dioxide 101 FAQs  

NLE Websites -- All DOE Office Websites (Extended Search)

are the primary sources of CO2? are the primary sources of CO2? Natural CO2 sources account for the majority of CO2 released into the atmosphere Natural CO2 sources account for the majority of CO2 released into the atmosphere. It is important to note that there are both natural CO2 sources and manmade (anthropogenic) CO2 sources. The primary natural CO2 sources include ocean release, animal and plant respiration, organic matter decomposition, forest fires, and volcanic eruptions, while the primary anthropogenic CO2 sources include fossil fuel burning, cement production, and farmland plowing. Natural CO2 sources account for the majority of CO2 released into the atmosphere. Oceans sometimes release dissolved CO2 into the atmosphere to maintain equilibrium between the two media. Oceans provide the greatest

372

Black carbon in Arctic snow and its effect on surface albedo  

E-Print Network (OSTI)

1 Black carbon in Arctic snow and its effect on surface albedo Stephen Warren, University wavelengths: ice is nearly transparent. Absorptive impurities: Black carbon (soot) Brown carbon (organics broadband albedo: 83% 71% (2) by addition of black carbon (BC) (20 ppb): 0.5% for r = 100 µm 1.6% for r

373

Tools for Forest Carbon Inventory, Management, and Reporting | Open Energy  

Open Energy Info (EERE)

Tools for Forest Carbon Inventory, Management, and Reporting Tools for Forest Carbon Inventory, Management, and Reporting Jump to: navigation, search Tool Summary LAUNCH TOOL Name: Tools for Carbon Inventory, Management, and Reporting Agency/Company /Organization: United States Forest Service, United States Department of Agriculture Sector: Land Focus Area: Forestry Topics: GHG inventory, Resource assessment Resource Type: Guide/manual, Lessons learned/best practices, Publications, Training materials, Software/modeling tools User Interface: Desktop Application, Website Website: nrs.fs.fed.us/carbon/tools/ Cost: Free Tools for Carbon Inventory, Management, and Reporting Screenshot References: Carbon Tools[1] Logo: Tools for Carbon Inventory, Management, and Reporting "Accurate estimates of carbon in forests are crucial for forest carbon

374

Carbon Value Analysis Tool (CVAT) | Open Energy Information  

Open Energy Info (EERE)

Carbon Value Analysis Tool (CVAT) Carbon Value Analysis Tool (CVAT) Jump to: navigation, search Tool Summary LAUNCH TOOL Name: Carbon Value Analysis Tool (CVAT) Agency/Company /Organization: World Resources Institute Sector: Energy, Land Topics: Co-benefits assessment, Finance, GHG inventory Resource Type: Software/modeling tools User Interface: Spreadsheet Website: www.wri.org/publication/carbon-value-analysis-tool Cost: Free Carbon Value Analysis Tool (CVAT) Screenshot References: CVAT[1] he Carbon Value Analysis Tool (CVAT) is a screening tool to help companies integrate the value of carbon dioxide emissions reductions into energy-related investment decisions. The tool has two main purposes: To test the sensitivity of a project's internal rate of return (IRR) to "carbon value" (the value of GHG emissions reductions). CVAT integrates this value into traditional financial analysis by ascribing a market price, either actual or projected, to carbon emissions reductions.

375

Nanostructuring of Microporous Carbons with Carbon Nanotubes for ...  

Science Conference Proceedings (OSTI)

Presentation Title, Nanostructuring of Microporous Carbons with Carbon Nanotubes for Efficient Carbon Dioxide Capture. Author(s), Stephen C. Hawkins,  ...

376

Carbon isotopes in peat, DOC, CO{sub 2}, and CH{sub 4} in a Holocene peatland on Dartmoor, southwest England  

Science Conference Proceedings (OSTI)

Carbon gases with younger {sup 14}C ages than those of the surrounding peat have been reported from continental boreal peatlands, a fact which suggests that significant movement of CO{sub 2}, CH{sub 4}, or DOC (dissolved organic carbon) and export of C via subsurface processes are not accounted for in most estimates of contributions to the C cycle. This paper tests the hypothesis that similar processes can occur in oceanic ombrotrophic mires where water and gas movement is theoretically minimal. Measurements of {sup 14}C and {delta}{sup 13}C in CO{sub 2}, CH{sub 4}, and DOC, and of tritium, are reported from depths to 250 cm at Tor Royal, a raised mire in southwest England. Radiocarbon ages of gases are 1,460 to 500 yr younger than those of peat from the same depths, and CO{sub 2} is consistently younger than CH{sub 4}. DOC is 1,260 to 830 yr younger than the peat, and significant amounts of tritium were found at all depths. Gas ages are mostly intermediate between the age of the peat and that of the DOC, which suggests that C is principally transported as DOC. However, some gases are younger than their associated DOC, which implies that movement of dissolved gases may also take place. {delta}{sup 13}C values in gases suggest that CO{sub 2} reduction is the major pathway for CH{sub 4} production. Transport of C in deep peats is likely to be a significant component in the overall C budget of ombrotrophic oceanic peatlands, and C export via discharge to ground or surface waters may be an important mechanism for gaseous C emissions.

Charman, D.J. [Univ. of Plymouth (United Kingdom). Dept. of Geographical Sciences; Aravena, R. [Univ. of Waterloo, Ontario (Canada). Dept. of Earth Sciences; Bryant, C.L.; Harkness, D.D. [Natural Environment Research Council Radiocarbon Lab., Glasgow (United Kingdom)

1999-06-01T23:59:59.000Z

377

U.S. Federal Offshore Associated-Dissolved Natural Gas, Wet After Lease  

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

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) U.S. Federal Offshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1990's 6,773 6,487 6,315 6,120 6,738 7,471 7,437 7,913 7,495 7,093 2000's 7,010 8,649 8,090 7,417 6,361 5,904 4,835 4,780 5,106 5,223 2010's 5,204 5,446 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease Separation, as of Dec. 31

378

Louisiana - South Onshore Associated-Dissolved Natural Gas, Wet After Lease  

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

South Onshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) South Onshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Louisiana - South Onshore Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 2,304 1980's 2,134 1,871 1,789 1,582 1,488 1,792 1,573 1,380 1,338 1,273 1990's 1,106 995 853 649 678 720 627 599 630 599 2000's 492 483 427 368 389 427 415 503 471 506 2010's 499 490 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease

379

Texas Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved  

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Texas Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1980's 10,832 10,753 9,735 9,340 9,095 9,205 1990's 8,999 8,559 8,667 7,880 7,949 7,787 8,160 7,786 7,364 7,880 2000's 6,833 6,089 6,387 6,437 6,547 7,003 7,069 7,530 7,559 8,762 2010's 10,130 13,507 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas Proved Reserves, Wet After Lease

380

Ice-Tethered Profiler Measurements of Dissolved Oxygen under Permanent Ice Cover in the Arctic Ocean  

Science Conference Proceedings (OSTI)

Four ice-tethered profilers (ITPs), deployed between 2006 and 2009, have provided year-round dissolved oxygen (DO) measurements from the surface mixed layer to 760-m depth under the permanent sea ice cover in the Arctic Ocean. These ITPs drifted ...

M.-L. Timmermans; R. Krishfield; S. Laney; J. Toole

2010-11-01T23:59:59.000Z

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

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.

382

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

383

Evaluation of a vertical continuous centrifuge for clarification of HTGR dissolver slurries  

Science Conference Proceedings (OSTI)

A series of statistically designed centrifuge performance tests was conducted to evaluate the solid-liquid separation efficiency of a vertical continuous centrifuge. Test results show that 100% of the particles greater than 4 microns in diameter were removed from simulated HTGR fuel reprocessing dissolver solutions. Centrifugal force and liquid density are the principal variables affecting separation efficiency.

Olguin, L.J.

1980-03-01T23:59:59.000Z

384

PROCESS FOR DISSOLVING BINARY URANIUM-ZIRCONIUM OR ZIRCONIUM-BASE ALLOYS  

DOE Patents (OSTI)

A process of dissolving uranium-- zirconium and zircaloy alloys, e.g. jackets of fuel elements, with an anhydrous hydrogen fluoride containing from 10 to 32% by weight of hydrogen chloride at between 400 and 450 deg C., preferably while in contact with a fluidized inert powder, such as calcium fluoride is described. (AEC)

Jonke, A.A.; Barghusen, J.J.; Levitz, N.M.

1962-08-14T23:59:59.000Z

385

Total Dissolved Gas Monitoring in Chum Salmon Spawning Gravels Below Bonneville Dam  

DOE Green Energy (OSTI)

At the request of the U.S. Army Corps of Engineers (Portland District), Pacific Northwest National Laboratory (PNNL) conducted research to determine whether total dissolved gas concentrations are elevated in chum salmon redds during spring spill operations at Bonneville Dam. The study involved monitoring the total dissolved gas levels at egg pocket depth and in the river at two chum salmon spawning locations downstream from Bonneville Dam. Dissolved atmospheric gas supersaturation generated by spill from Bonneville Dam may diminish survival of chum (Oncorhynchus keta) salmon when sac fry are still present in the gravel downstream from Bonneville Dam. However, no previous work has been conducted to determine whether total dissolved gas (TDG) levels are elevated during spring spill operations within incubation habitats. The guidance used by hydropower system managers to provide protection for pre-emergent chum salmon fry has been to limit TDG to 105% after allowing for depth compensation. A previous literature review completed in early 2006 shows that TDG levels as low as 103% have been documented to cause mortality in sac fry. Our study measured TDG in the incubation environment to evaluate whether these levels were exceeded during spring spill operations. Total dissolved gas levels were measured within chum salmon spawning areas near Ives Island and Multnomah Falls on the Columbia River. Water quality sensors screened at egg pocket depth and to the river were installed at both sites. At each location, we also measured dissolved oxygen, temperature, specific conductance, and water depth to assist with the interpretation of TDG results. Total dissolved gas was depth-compensated to determine when levels were high enough to potentially affect sac fry. This report provides detailed descriptions of the two study sites downstream of Bonneville Dam, as well as the equipment and procedures employed to monitor the TDG levels at the study sites. Results of the monitoring at both sites are then presented in both text and graphics. The findings and recommendations for further research are discussed, followed by a listing of the references cited in the report.

Arntzen, Evan V.; Geist, David R.; Panther, Jennifer L.; Dawley, Earl

2007-01-30T23:59:59.000Z

386

STRIPPING OF URANIUM FROM ORGANIC EXTRACTANTS  

DOE Patents (OSTI)

A liquid-liquid extraction method is given for recovering uranium values from uranium-containing solutions. Uranium is removed from a uranium-containing organic solution by contacting said organic solution with an aqueous ammonium carbonate solution substantially saturated in uranium values. A uranium- containing precipitate is thereby formed which is separated from the organic and aqueous phases. Uranium values are recovered from this separated precipitate. (AE C)

Crouse, D.J. Jr.

1962-09-01T23:59:59.000Z

387

Carbon Steels  

Science Conference Proceedings (OSTI)

Table 1   Corrosion rates of carbon steel at various locations...Vancouver Island, BC, Canada Rural marine 13 0.5 Detroit, MI Industrial 14.5 0.57 Fort Amidor Pier, CZ Marine 14.5 0.57 Morenci, MI Urban 19.5 0.77 Potter County, PA Rural 20 0.8 Waterbury, CT Industrial 22.8 0.89 State College, PA Rural 23 0.9 Montreal, QC, Canada Urban 23 0.9 Durham, NH Rural 28 1.1...

388

AirShares EU Carbon Allowances Fund | Open Energy Information  

Open Energy Info (EERE)

AirShares EU Carbon Allowances Fund AirShares EU Carbon Allowances Fund Jump to: navigation, search Name AirShares EU Carbon Allowances Fund Place New York, New York Zip 10170 Product AirShares is a commodity pool for exchange-traded futures contracts for EUAs. References AirShares EU Carbon Allowances Fund[1] LinkedIn Connections CrunchBase Profile No CrunchBase profile. Create one now! This article is a stub. You can help OpenEI by expanding it. AirShares EU Carbon Allowances Fund is a company located in New York, New York . References ↑ "AirShares EU Carbon Allowances Fund" Retrieved from "http://en.openei.org/w/index.php?title=AirShares_EU_Carbon_Allowances_Fund&oldid=341942" Categories: Clean Energy Organizations Companies Organizations Stubs What links here Related changes

389

Unsteady-state material balance model for a continuous rotary dissolver  

Science Conference Proceedings (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

390

On carbon footprints and growing energy use  

SciTech Connect

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

391

China-NIES Low-Carbon Society Scenarios 2050 | Open Energy Information  

Open Energy Info (EERE)

China-NIES Low-Carbon Society Scenarios 2050 Jump to: navigation, search Name China-NIES Low-Carbon Society Scenarios 2050 AgencyCompany Organization National Institute for...

392

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

393

MIDWEST REGIONAL CARBON SEQUESTRATION PARTNERSHIP THE UNITED  

NLE Websites -- All DOE Office Websites (Extended Search)

MIDWEST REGIONAL CARBON SEQUESTRATION PARTNERSHIP THE UNITED S T A T E S 2012 ATLAS CARBON UTILIZATION AND STORAGE Midwest Regional Carbon Sequestration Partnership The Midwest Regional Carbon Sequestration Partnership (MRCSP) region consists of nine neighboring states: Indiana, Kentucky, Maryland, Michigan, New Jersey, New York, Ohio, Pennsylvania, and West Virginia. Battelle Memorial Institute leads MRCSP, which includes nearly 40 organizations from the research community, energy industry, universities, non-government, and government organizations. The region has a diverse range of CO 2 sources and many opportunities for reducing CO 2 emissions through geologic storage and/or EOR. Potential locations for geologic storage in the MRCSP states extend from the deep rock formations in the broad

394

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: (i) an x-ray density of at least 2.00 grams per cubic centimeters, (ii) a closed porosity of no greater than 5%, and (iii) an open porosity of no greater than 47%; and (b) graphite having the following properties: (i) an x-ray density of at least 2.20 grams per cubic centimeters, (ii) a closed porosity of no greater than 5%, and (iii) 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 counterelectrode.

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

1997-01-01T23:59:59.000Z

395

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

396

Autonomous observations of the ocean biological carbon pump  

Science Conference Proceedings (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

397

Carbon Sequestration Project Portfolio  

NLE Websites -- All DOE Office Websites (Extended Search)

Home > Technologies > Carbon Storage > Reference Shelf > Project Portfolio Home > Technologies > Carbon Storage > Reference Shelf > Project Portfolio Carbon Storage 2011 Carbon Storage Project Portfolio Table of Contents CARBON STORAGE OVERVIEW Carbon Storage Program Contacts [PDF-26KB] Carbon Storage Projects National Map [PDF-169KB] State Projects Summary Table [PDF-39KB] Carbon Storage Program Structure [PDF-181KB] Selected Carbon Sequestration Program Papers and Publications The U.S. Department of Energy's R&D Program to Reduce Greenhouse Gas Emissions Through Beneficial Uses of Carbon Dioxide (2011) [PDF-3.3MB] Greenhouse Gas Science and Technology Carbon Capture and Sequestration: The U.S. Department of Energy's R&D Efforts to Characterize Opportunities for Deep Geologic Storage of Carbon Dioxide in Offshore Resources (2011) [PDF-445KB]

398

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

399

Carbon Dioxide (CO2)  

NLE Websites -- All DOE Office Websites (Extended Search)

Carbon Dioxide (CO2) Carbon Dioxide (CO2) Gateway Pages to Carbon Dioxide Data Modern records and ice core records back 2000 years 800,000 year records from ice cores Other...

400

Campus Carbon Calculator | Open Energy Information  

Open Energy Info (EERE)

Campus Carbon Calculator Campus Carbon Calculator Jump to: navigation, search Tool Summary Name: Campus Carbon Calculator Agency/Company /Organization: Clean Air-Cool Planet Phase: Create a Vision, Determine Baseline, Develop Goals User Interface: Spreadsheet Website: www.cleanair-coolplanet.org/toolkit/inv-calculator.php The Campus Carbon Calculator(tm), Version 6.4, is now available for download. Version 6.4 includes new features, updates and corrections - including greatly expanded projection and solutions modules, designed to aid schools that have completed greenhouse gas inventories in developing long term, comprehensive climate action plans based on those inventories. The new modules facilitate analysis of carbon reduction options, determining project payback times, net present value, cost per ton reduced,

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

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

402

Carbon Initiative for Development (Ci-Dev) | Open Energy Information  

Open Energy Info (EERE)

Ci-Dev) Ci-Dev) Jump to: navigation, search Name Carbon Initiative for Development (Ci-Dev) Agency/Company /Organization World Bank Sector Climate Topics Finance, GHG inventory, Low emission development planning Website http://wbcarbonfinance.org/Rou References Carbon Initiative for Development (Ci-Dev)[1] "The World Bank is proposing a new initiative, the Carbon Initiative for Development (Ci-Dev), which aims at helping low-income countries create sustainable access to financing for low-carbon investments through carbon markets. This initiative has three components: A Readiness Fund will support carbon capacity building, knowledge development and advocacy work for improving carbon market mechanisms, asset creation, and developing innovative approaches to leveraging carbon

403

Carbon dioxide and climate  

SciTech Connect

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.

1990-10-01T23:59:59.000Z

404

DOE Carbon Sequestration Program  

NLE Websites -- All DOE Office Websites (Extended Search)

Carbon Sequestration Program Charles E. Schmidt Carbon Sequestration Product Manager National Energy Technology Laboratory David J. Beecy Director, Office of Environmental Systems...

405

Catalyzing Low Carbon Growth in Developing Countries | Open Energy  

Open Energy Info (EERE)

Catalyzing Low Carbon Growth in Developing Countries Catalyzing Low Carbon Growth in Developing Countries Jump to: navigation, search Tool Summary Name: Catalyzing Low Carbon Growth in Developing Countries: Public Finance Mechanisms to scale up private sector investment in climate solutions Agency/Company /Organization: United Nations Environment Programme Sector: Energy Focus Area: Renewable Energy, Energy Efficiency Topics: Finance, Low emission development planning, Policies/deployment programs Resource Type: Guide/manual Website: sefi.unep.org/fileadmin/media/sefi/docs/publications/PublicPrivateWeb. Catalyzing Low Carbon Growth in Developing Countries: Public Finance Mechanisms to scale up private sector investment in climate solutions Screenshot References: Catalyzing Low Carbon Growth in Developing Countries[1]

406

Carbon Nanotube Nanocomposites, Methods of Making Carbon ...  

This technology describes methods to fabricate supercapacitors using aligned carbon nanotubes that are decorated with metal oxide or nitride ...

407

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

408

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 of group schemes 8 2.6 Monitoring 9 2.7 Carbon statements and reporting 9 2.8 Woodland Carbon Code trademark 10 3. Carbon sequestration 11 3.1 Units of carbon calculation 11 3.2 Carbon baseline 11 3.3 Carbon

409

Carbon Code Requirements for voluntary carbon sequestration projects  

E-Print Network (OSTI)

Woodland Carbon Code Requirements for voluntary carbon sequestration projects ® Version 1.1 July.6 Monitoring 8 2.7 Carbon statements and reporting 8 2.8 Woodland Carbon Code trademark 9 3. Carbon sequestration 10 3.1 Units of carbon calculation 10 3.2 Carbon baseline 10 3.3 Carbon leakage 11 3.4 Project

410

U.S. Associated-Dissolved Natural Gas, Wet After Lease Separation, New  

Gasoline and Diesel Fuel Update (EIA)

Reservoir Discoveries in Old Fields (Billion Cubic Feet) Reservoir Discoveries in Old Fields (Billion Cubic Feet) U.S. Associated-Dissolved Natural Gas, Wet After Lease Separation, New Reservoir Discoveries in Old Fields (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 264 1980's 369 271 365 326 296 341 189 155 339 174 1990's 250 334 292 163 202 634 338 187 218 424 2000's 249 477 331 124 97 79 65 73 820 169 2010's 186 160 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages: Associated-Dissolved Natural Gas New Reservoir Discoveries in Old Fields, Wet After Lease Separation

411

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

Science Conference Proceedings (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

412

EPRI Dissolved Gas Analysis Guide for High-Voltage Cables and Transformers  

Science Conference Proceedings (OSTI)

Dissolved gas analysis (DGA) is deemed to be the most economical and reliable diagnostic test for both cables and transformers, and it is finding widespread application worldwide. The general subject of DGA has continued to receive considerable attention for several decades. While there is commonality between cable and transformer DGA and the oil-paper insulating system, there are marked differences with respect to DGA due to the differing designs, materials, and operating conditions associated with ...

2012-12-20T23:59:59.000Z

413

EPRI Dissolved Gas Analysis Guide for High Voltage Cables and Transformers – 2013 Update  

Science Conference Proceedings (OSTI)

Dissolved gas analysis (DGA) is deemed to be an economical and reliable diagnostic test for both cables and transformers and is finding widespread application worldwide. The general subject of DGA has continued to receive considerable attention for several decades. While there is commonality between cable and transformer DGA and the oil-paper insulating system, there are marked differences with respect to DGA due to the differing designs, materials, and operating conditions associated with the two ...

2013-12-20T23:59:59.000Z

414

Dissolved Gas Analysis (DGA) by EPRI Disposable Oil Sampling System (EDOSS)  

Science Conference Proceedings (OSTI)

The utility industry has increasingly applied dissolved gas analysis (DGA) to assess the condition of fluid-filled equipment. Modifications to the EPRI Pressurized Oil Sampling System (EPOSS), a novel DGA method developed in 1983, have rendered the system more cost-effective without compromising its accuracy and precision. Designated the EPRI Disposable Oil Sampling System, EDOSS safely operates with all types of fluid-filled equipment under most weather conditions.

1998-10-12T23:59:59.000Z

415

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

416

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

417

Brazil-Pathways to a Low Carbon Economy | Open Energy Information  

Open Energy Info (EERE)

search Name Pathways to a Low Carbon Economy for Brazil AgencyCompany Organization McKinsey and Company Topics Implementation, Low emission development planning, Policies...

418

New Mexico Associated-Dissolved Natural Gas, Wet After Lease Separation,  

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) New Mexico Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 1,823 1980's 1,689 1,649 1,520 1,503 1,569 1,490 1,446 1,445 1,453 1,378 1990's 1,435 1,554 1,597 1,585 1,641 1,678 1,693 1,420 1,443 1,578 2000's 1,588 1,447 1,482 1,545 1,578 1,661 1,772 1,841 1,755 1,982 2010's 2,213 2,552 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages:

419

New Mexico - East Associated-Dissolved Natural Gas, Wet After Lease  

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) New Mexico - East Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 1,672 1980's 1,533 1,499 1,374 1,323 1,375 1,309 1,232 1,232 1,194 1,200 1990's 1,251 1,398 1,470 1,478 1,544 1,559 1,585 1,314 1,345 1,486 2000's 1,473 1,348 1,379 1,456 1,488 1,563 1,690 1,754 1,669 1,900 2010's 2,108 2,409 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages:

420

Lower 48 States Associated-Dissolved Natural Gas, Wet After Lease  

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

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Lower 48 States Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 32,208 1980's 33,443 32,870 31,268 31,286 30,282 29,515 28,684 27,457 26,609 26,611 1990's 26,242 25,088 24,701 23,551 23,913 24,532 24,715 24,666 23,385 24,206 2000's 23,065 23,232 23,165 22,285 21,180 21,874 20,754 21,916 22,396 25,290 2010's 27,850 34,288 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014

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

Alaska Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved  

Gasoline and Diesel Fuel Update (EIA)

Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Alaska Associated-Dissolved Natural Gas, Wet After Lease Separation, Proved Reserves (Billion Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3 Year-4 Year-5 Year-6 Year-7 Year-8 Year-9 1970's 27,217 1980's 28,567 28,676 30,814 30,408 30,356 31,092 30,893 30,732 6,269 6,198 1990's 6,927 6,729 6,723 6,494 6,487 6,265 6,080 7,716 7,275 7,209 2000's 6,768 6,592 6,376 6,267 6,469 6,362 8,886 10,752 6,627 8,093 2010's 7,896 8,535 - = No Data Reported; -- = Not Applicable; NA = Not Available; W = Withheld to avoid disclosure of individual company data. Release Date: 8/1/2013 Next Release Date: 8/1/2014 Referring Pages:

422

Overview of Carbon Storage Research | Department of Energy  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Overview of Overview of Carbon Storage Research Overview of Carbon Storage Research The Carbon Storage Program is focused on ensuring the safe and permanent storage and/or utilization of CO2 captured from point sources. The Carbon Storage Program is focused on ensuring the safe and permanent storage and/or utilization of CO2 captured from point sources. Roughly one third of the United States' carbon emissions come from power plants and other large point sources, such as industrial facilities. The Carbon Storage Program is focused on ensuring the safe and permanent storage and/or utilization of CO2 captured from point sources. This effort is organized into two broad areas: Cooperative Advancement, which involves working with other organizations and governments to advance CCS worldwide, and

423

Organizations and Networks | Open Energy Information  

Open Energy Info (EERE)

Organizations and Networks Organizations and Networks (Redirected from Gateway:International/Networks) Jump to: navigation, search Registered Technical and Research Organizations Networks Climate Eval "The website promotes active debate on areas relevant to evaluation of climate change and development evaluation by bringing relevant topics to a peer to peer discussion forum." Coordinated Low Emissions Assistance Network (CLEAN) CLEAN aims to improve communication and coordination by bringing together national and international organizations that are assisting developing countries with preparation and implementation of low greenhouse gas emission plans and strategies. This includes support for technology needs assessments, for low carbon and clean energy development plans, and

424

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

425

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

426

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

427

Mechanomutable Carbon Nanotube Arrays  

Science Conference Proceedings (OSTI)

About this Abstract. Meeting, 2010 TMS Annual Meeting & Exhibition. Symposium , Polymer Nanocomposites. Presentation Title, Mechanomutable Carbon ...

428

CALCIUM CARBONATE PRODUCTION BY COCCOLITHOPHORID ALGAE IN LONG TERM CARBON DIOXIDE SEQUESTRATION  

DOE Green Energy (OSTI)

Predictions of increasing levels of anthropogenic carbon dioxide (CO{sub 2}) and the specter of global warming have intensified research efforts to identify ways to sequester carbon. A number of novel avenues of research are being considered, including bioprocessing methods to promote and accelerate biosequestration of CO{sub 2} from the environment through the growth of organisms such as coccolithophorids, which are capable of sequestering CO{sub 2} relatively permanently. Calcium and magnesium carbonates are currently the only proven, long-term storage reservoirs for carbon. Whereas organic carbon is readily oxidized and releases CO{sub 2} through microbial decomposition on land and in the sea, carbonates can sequester carbon over geologic time scales. This proposal investigates the use of coccolithophorids--single-celled, marine algae that are the major global producers of calcium carbonate--to sequester CO{sub 2} emissions from power plants. Cultivation of coccolithophorids for calcium carbonate (CaCO{sub 3}) precipitation is environmentally benign and results in a stable product with potential commercial value. Because this method of carbon sequestration does not impact natural ecosystem dynamics, it avoids controversial issues of public acceptability and legality associated with other options such as direct injection of CO{sub 2} into the sea and ocean fertilization. Consequently, cultivation of coccolithophorids could be carried out immediately and the amount of carbon sequestered as CaCO{sub 3} could be readily quantified. The significant advantages of this approach warrant its serious investigation. The major goals of the proposed research are to identify the growth conditions that will result in the maximum amount of CO{sub 2} sequestration through coccolithophorid calcite production and to evaluate the costs/benefits of using coccolithophorid cultivation ponds or bioreactors to abate CO{sub 2} emissions from power plants.

V. J. Fabry

2003-10-30T23:59:59.000Z

429

CALCIUM CARBONATE PRODUCTION BY COCCOLITHOPHORID ALGAE IN LONG TERM, CARBON DIOXIDE SEQUESTRATION  

DOE Green Energy (OSTI)

Predictions of increasing levels of anthropogenic carbon dioxide (CO{sub 2}) and the specter of global warming have intensified research efforts to identify ways to sequester carbon. A number of novel avenues of research are being considered, including bioprocessing methods to promote and accelerate biosequestration of CO{sub 2} from the environment through the growth of organisms such as coccolithophorids, which are capable of sequestering CO{sub 2} relatively permanently. Calcium and magnesium carbonates are currently the only proven, long-term storage reservoirs for carbon. Whereas organic carbon is readily oxidized and releases CO{sub 2} through microbial decomposition on land and in the sea, carbonates can sequester carbon over geologic time scales. This proposal investigates the use of coccolithophorids--single-celled, marine algae that are the major global producers of calcium carbonate--to sequester CO{sub 2} emissions from power plants. Cultivation of coccolithophorids for calcium carbonate (CaCO{sub 3}) precipitation is environmentally benign and results in a stable product with potential commercial value. Because this method of carbon sequestration does not impact natural ecosystem dynamics, it avoids controversial issues of public acceptability and legality associated with other options such as direct injection of CO{sub 2} into the sea and ocean fertilization. Consequently, cultivation of coccolithophorids could be carried out immediately and the amount of carbon sequestered as CaCO{sub 3} could be readily quantified. The significant advantages of this approach warrant its serious investigation. The major goals of the proposed research are to identify the growth conditions that will result in the maximum amount of CO{sub 2} sequestration through coccolithophorid calcite production and to evaluate the costs/benefits of using coccolithophorid cultivation ponds or bioreactors to abate CO{sub 2} emissions from power plants.

V.J. Fabry

2004-10-30T23:59:59.000Z

430

CALCIUM CARBONATE PRODUCTION BY COCCOLITHAPHORID ALGAE IN LONG TERM, CARBON DIOXIDE SEQUESTRATION  

SciTech Connect

Predictions of increasing levels of anthropogenic carbon dioxide (CO{sub 2}) and the specter of global warming have intensified research efforts to identify ways to sequester carbon. A number of novel avenues of research are being considered, including bioprocessing methods to promote and accelerate biosequestration of CO{sub 2} from the environment through the growth of organisms such as coccolithophorids, which are capable of sequestering CO{sub 2} relatively permanently. Calcium and magnesium carbonates are currently the only proven, long-term storage reservoirs for carbon. Whereas organic carbon is readily oxidized and releases CO{sub 2} through microbial decomposition on land and in the sea, carbonates can sequester carbon over geologic time scales. This proposal investigates the use of coccolithophorids--single-celled, marine algae that are the major global producers of calcium carbonate--to sequester CO{sub 2} emissions from power plants. Cultivation of coccolithophorids for calcium carbonate (CaCO{sub 3}) precipitation is environmentally benign and results in a stable product with potential commercial value. Because this method of carbon sequestration does not impact natural ecosystem dynamics, it avoids controversial issues of public acceptability and legality associated with other options such as direct injection of CO{sub 2} into the sea and ocean fertilization. Consequently, cultivation of coccolithophorids could be carried out immediately and the amount of carbon sequestered as CaCO{sub 3} could be readily quantified. The significant advantages of this approach warrant its serious investigation. The major goals of the proposed research are to identify the growth conditions that will result in the maximum amount of CO{sub 2} sequestration through coccolithophorid calcite production and to evaluate the costs/benefits of using coccolithophorid cultivation ponds to abate CO{sub 2} emissions from power plants.

V. J.Fabry

2004-01-30T23:59:59.000Z

431

CALCIUM CARBONATE PRODUCTION BY COCCOLITHOPHORID ALGAE IN LONG TERM, CARBON DIOXIDE SEQUESTRATION  

SciTech Connect

Predictions of increasing levels of anthropogenic carbon dioxide (CO{sub 2}) and the specter of global warming have intensified research efforts to identify ways to sequester carbon. A number of novel avenues of research are being considered, including bioprocessing methods to promote and accelerate biosequestration of CO{sub 2} from the environment through the growth of organisms such as coccolithophorids, which are capable of sequestering CO{sub 2} relatively permanently. Calcium and magnesium carbonates are currently the only proven, long-term storage reservoirs for carbon. Whereas organic carbon is readily oxidized and releases CO{sub 2} through microbial decomposition on land and in the sea, carbonates can sequester carbon over geologic time scales. This proposal investigates the use of coccolithophorids--single-celled, marine algae that are the major global producers of calcium carbonate--to sequester CO{sub 2} emissions from power plants. Cultivation of coccolithophorids for calcium carbonate (CaCO{sub 3}) precipitation is environmentally benign and results in a stable product with potential commercial value. Because this method of carbon sequestration does not impact natural ecosystem dynamics, it avoids controversial issues of public acceptability and legality associated with other options such as direct injection of CO{sub 2} into the sea and ocean fertilization. Consequently, cultivation of coccolithophorids could be carried out immediately and the amount of carbon sequestered as CaCO{sub 3} could be readily quantified. The significant advantages of this approach warrant its serious investigation. The major goals of the proposed research are to identify the growth conditions that will result in the maximum amount of CO{sub 2} sequestration through coccolithophorid calcite production and to evaluate the costs/benefits of using coccolithophorid cultivation ponds to abate CO{sub 2} emissions from power plants.

V.J. Fabry, Ph.D.

2001-12-15T23:59:59.000Z

432

CALCIUM CARBONATE PRODUCTION BY COCCOLITHOPHORID ALGAE IN LONG TERM, CARBON DIOXIDE SEQUESTRATION  

SciTech Connect

Predictions of increasing levels of anthropogenic carbon dioxide (CO{sub 2}) and the specter of global warming have intensified research efforts to identify ways to sequester carbon. A number of novel avenues of research are being considered, including bioprocessing methods to promote and accelerate biosequestration of CO{sub 2} from the environment through the growth of organisms such as coccolithophorids, which are capable of sequestering CO{sub 2} relatively permanently. Calcium and magnesium carbonates are currently the only proven, long-term storage reservoirs for carbon. Whereas organic carbon is readily oxidized and releases CO{sub 2} through microbial decomposition on land and in the sea, carbonates can sequester carbon over geologic time scales. This proposal investigates the use of coccolithophorids--single-celled, marine algae that are the major global producers of calcium carbonate--to sequester CO{sub 2} emissions from power plants. Cultivation of coccolithophorids for calcium carbonate (CaCO{sub 3}) precipitation is environmentally benign and results in a stable product with potential commercial value. Because this method of carbon sequestration does not impact natural ecosystem dynamics, it avoids controversial issues of public acceptability and legality associated with other options such as direct injection of CO{sub 2} into the sea and ocean fertilization. Consequently, cultivation of coccolithophorids could be carried out immediately and the amount of carbon sequestered as CaCO{sub 3} could be readily quantified. The significant advantages of this approach warrant its serious investigation. The major goals of the proposed research are to identify the growth conditions that will result in the maximum amount of CO{sub 2} sequestration through coccolithophorid calcite production and to evaluate the costs/benefits of using coccolithophorid cultivation ponds to abate CO{sub 2} emissions from power plants.

V.J. Fabry, Ph.D.

2003-07-15T23:59:59.000Z

433

CALCIUM CARBONATE PRODUCTION BY COCCOLITHOPHORID ALGAE IN LONG TERM, CARBON DIOXIDE SEQUESTRATION  

SciTech Connect

Predictions of increasing levels of anthropogenic carbon dioxide (CO{sub 2}) and the specter of global warming have intensified research efforts to identify ways to sequester carbon. A number of novel avenues of research are being considered, including bioprocessing methods to promote and accelerate biosequestration of CO{sub 2} from the environment through the growth of organisms such as coccolithophorids, which are capable of sequestering CO{sub 2} relatively permanently. Calcium and magnesium carbonates are currently the only proven, long-term storage reservoirs for carbon. Whereas organic carbon is readily oxidized and releases CO{sub 2} through microbial decomposition on land and in the sea, carbonates can sequester carbon over geologic time scales. This proposal investigates the use of coccolithophorids--single-celled, marine algae that are the major global producers of calcium carbonate--to sequester CO{sub 2} emissions from power plants. Cultivation of coccolithophorids for calcium carbonate (CaCO{sub 3}) precipitation is environmentally benign and results in a stable product with potential commercial value. Because this method of carbon sequestration does not impact natural ecosystem dynamics, it avoids controversial issues of public acceptability and legality associated with other options such as direct injection of CO{sub 2} into the sea and ocean fertilization. Consequently, cultivation of coccolithophorids could be carried out immediately and the amount of carbon sequestered as CaCO{sub 3} could be readily quantified. The significant advantages of this approach warrant its serious investigation. The major goals of the proposed research are to identify the growth conditions that will result in the maximum amount of CO{sub 2} sequestration through coccolithophorid calcite production and to evaluate the costs/benefits of using coccolithophorid cultivation ponds to abate CO{sub 2} emissions from power plants.

V.J. Fabry, Ph.D.

2001-09-10T23:59:59.000Z

434

CALCIUM CARBONATE PRODUCTION BY COCCOLITHOPHORID ALGAE IN LONG TERM, CARBON DIOXIDE SEQUESTRATION  

SciTech Connect

Predictions of increasing levels of anthropogenic carbon dioxide (CO{sub 2}) and the specter of global warming have intensified research efforts to identify ways to sequester carbon. A number of novel avenues of research are being considered, including bioprocessing methods to promote and accelerate biosequestration of CO{sub 2} from the environment through the growth of organisms such as coccolithophorids, which are capable of sequestering CO{sub 2} relatively permanently. Calcium and magnesium carbonates are currently the only proven, long-term storage reservoirs for carbon. Whereas organic carbon is readily oxidized and releases CO{sub 2} through microbial decomposition on land and in the sea, carbonates can sequester carbon over geologic time scales. This proposal investigates the use of coccolithophorids--single-celled, marine algae that are the major global producers of calcium carbonate--to sequester CO{sub 2} emissions from power plants. Cultivation of coccolithophorids for calcium carbonate (CaCO{sub 3}) precipitation is environmentally benign and results in a stable product with potential commercial value. Because this method of carbon sequestration does not impact natural ecosystem dynamics, it avoids controversial issues of public acceptability and legality associated with other options such as direct injection of CO{sub 2} into the sea and ocean fertilization. Consequently, cultivation of coccolithophorids could be carried out immediately and the amount of carbon sequestered as CaCO{sub 3} could be readily quantified. The significant advantages of this approach warrant its serious investigation. The major goals of the proposed research are to identify the growth conditions that will result in the maximum amount of CO{sub 2} sequestration through coccolithophorid calcite production and to evaluate the costs/benefits of using coccolithophorid cultivation ponds to abate CO{sub 2} emissions from power plants.

V.J. Fabry, Ph.D.

2003-04-15T23:59:59.000Z

435

Calcium Carbonate Production by Coccolithophorid Algae in Long Term, Carbon Dioxide Sequestration  

SciTech Connect

Predictions of increasing levels of anthropogenic carbon dioxide (CO{sub 2}) and the specter of global warming have intensified research efforts to identify ways to sequester carbon. A number of novel avenues of research are being considered, including bioprocessing methods to promote and accelerate biosequestration of CO{sub 2} from the environment through the growth of organisms such as coccolithophorids, which are capable of sequestering CO{sub 2} relatively permanently. Calcium and magnesium carbonates are currently the only proven, long-term storage reservoirs for carbon. Whereas organic carbon is readily oxidized and releases CO{sub 2} through microbial decomposition on land and in the sea, carbonates can sequester carbon over geologic time scales. This proposal investigates the use of coccolithophorids--single-celled, marine algae that are the major global producers of calcium carbonate--to sequester CO{sub 2} emissions from power plants. Cultivation of coccolithophorids for calcium carbonate (CaCO{sub 3}) precipitation is environmentally benign and results in a stable product with potential commercial value. Because this method of carbon sequestration does not impact natural ecosystem dynamics, it avoids controversial issues of public acceptability and legality associated with other options such as direct injection of CO{sub 2} into the sea and ocean fertilization. Consequently, cultivation of coccolithophorids could be carried out immediately and the amount of carbon sequestered as CaCO{sub 3} could be readily quantified. The significant advantages of this approach warrant its serious investigation. The major goals of the proposed research are to identify the growth conditions that will result in the maximum amount of CO{sub 2} sequestration through coccolithophorid calcite production and to evaluate the costs/benefits of using coccolithophorid cultivation ponds to abate CO{sub 2} emissions from power plants.

V.J. Fabry

2005-04-29T23:59:59.000Z

436

CALCIUM CARBONATE PRODUCTION BY COCCOLITHOPHORID ALGAE IN LONG TERM, CARBON DIOXIDE SEQUESTRATION  

SciTech Connect

Predictions of increasing levels of anthropogenic carbon dioxide (CO{sub 2}) and the specter of global warming have intensified research efforts to identify ways to sequester carbon. A number of novel avenues of research are being considered, including bioprocessing methods to promote and accelerate biosequestration of CO{sub 2} from the environment through the growth of organisms such as coccolithophorids, which are capable of sequestering CO{sub 2} relatively permanently. Calcium and magnesium carbonates are currently the only proven, long-term storage reservoirs for carbon. Whereas organic carbon is readily oxidized and releases CO{sub 2} through microbial decomposition on land and in the sea, carbonates can sequester carbon over geologic time scales. This proposal investigates the use of coccolithophorids--single-celled, marine algae that are the major global producers of calcium carbonate--to sequester CO{sub 2} emissions from power plants. Cultivation of coccolithophorids for calcium carbonate (CaCO{sub 3}) precipitation is environmentally benign and results in a stable product with potential commercial value. Because this method of carbon sequestration does not impact natural ecosystem dynamics, it avoids controversial issues of public acceptability and legality associated with other options such as direct injection of CO{sub 2} into the sea and ocean fertilization. Consequently, cultivation of coccolithophorids could be carried out immediately and the amount of carbon sequestered as CaCO{sub 3} could be readily quantified. The significant advantages of this approach warrant its serious investigation. The major goals of the proposed research are to identify the growth conditions that will result in the maximum amount of CO{sub 2} sequestration through coccolithophorid calcite production and to evaluate the costs/benefits of using coccolithophorid cultivation ponds to abate CO{sub 2} emissions from power plants.

V.J. Fabry, Ph.D.

2002-12-15T23:59:59.000Z

437

Calcium Carbonate Production by Coccolithophorid Algae in Long Term, Carbon Dioxide Sequestration  

SciTech Connect

Predictions of increasing levels of anthropogenic carbon dioxide (CO{sub 2}) and the specter of global warming have intensified research efforts to identify ways to sequester carbon. A number of novel avenues of research are being considered, including bioprocessing methods to promote and accelerate biosequestration of CO{sub 2} from the environment through the growth of organisms such as coccolithophorids, which are capable of sequestering CO{sub 2} relatively permanently. Calcium and magnesium carbonates are currently the only proven, long-term storage reservoirs for carbon. Whereas organic carbon is readily oxidized and releases CO{sub 2} through microbial decomposition on land and in the sea, carbonates can sequester carbon over geologic time scales. This proposal investigates the use of coccolithophorids--single-celled, marine algae that are the major global producers of calcium carbonate--to sequester CO{sub 2} emissions from power plants. Cultivation of coccolithophorids for calcium carbonate (CaCO{sub 3}) precipitation is environmentally benign and results in a stable product with potential commercial value. Because this method of carbon sequestration does not impact natural ecosystem dynamics, it avoids controversial issues of public acceptability and legality associated with other options such as direct injection of CO{sub 2} into the sea and ocean fertilization. Consequently, cultivation of coccolithophorids could be carried out immediately and the amount of carbon sequestered as CaCO{sub 3} could be readily quantified. The significant advantages of this approach warrant its serious investigation. The major goals of the proposed research are to identify the growth conditions that will result in the maximum amount of CO{sub 2} sequestration through coccolithophorid calcite production and to evaluate the costs/benefits of using coccolithophorid cultivation ponds to abate CO{sub 2} emissions from power plants.

V. J. Fabry

2006-06-30T23:59:59.000Z

438

CALCIUM CARBONATE PRODUCTION BY COCCOLITHOPHORID ALGAE IN LONG TERM, CARBON DIOXIDE SEQUESTRATION  

SciTech Connect

Predictions of increasing levels of anthropogenic carbon dioxide (CO{sub 2}) and the specter of global warming have intensified research efforts to identify ways to sequester carbon. A number of novel avenues of research are being considered, including bioprocessing methods to promote and accelerate biosequestration of CO{sub 2} from the environment through the growth of organisms such as coccolithophorids, which are capable of sequestering CO{sub 2} relatively permanently. Calcium and magnesium carbonates are currently the only proven, long-term storage reservoirs for carbon. Whereas organic carbon is readily oxidized and releases CO{sub 2} through microbial decomposition on land and in the sea, carbonates can sequester carbon over geologic time scales. This proposal investigates the use of coccolithophorids--single-celled, marine algae that are the major global producers of calcium carbonate--to sequester CO{sub 2} emissions from power plants. Cultivation of coccolithophorids for calcium carbonate (CaCO{sub 3}) precipitation is environmentally benign and results in a stable product with potential commercial value. Because this method of carbon sequestration does not impact natural ecosystem dynamics, it avoids controversial issues of public acceptability and legality associated with other options such as direct injection of CO{sub 2} into the sea and ocean fertilization. Consequently, cultivation of coccolithophorids could be carried out immediately and the amount of carbon sequestered as CaCO{sub 3} could be readily quantified. The significant advantages of this approach warrant its serious investigation. The major goals of the proposed research are to identify the growth conditions that will result in the maximum amount of CO{sub 2} sequestration through coccolithophorid calcite production and to evaluate the costs/benefits of using coccolithophorid cultivation ponds to abate CO{sub 2} emissions from power plants.

V.J. Fabry, Ph.D.

2002-07-09T23:59:59.000Z

439

CALCIUM CARBONATE PRODUCTION BY COCCOLITHOPHORID ALGAE IN LONG TERM, CARBON DIOXIDE SEQUESTRATION  

SciTech Connect

Predictions of increasing levels of anthropogenic carbon dioxide (CO{sub 2}) and the specter of global warming have intensified research efforts to identify ways to sequester carbon. A number of novel avenues of research are being considered, including bioprocessing methods to promote and accelerate biosequestration of CO{sub 2} from the environment through the growth of organisms such as coccolithophorids, which are capable of sequestering CO{sub 2} relatively permanently. Calcium and magnesium carbonates are currently the only proven, long-term storage reservoirs for carbon. Whereas organic carbon is readily oxidized and releases CO{sub 2} through microbial decomposition on land and in the sea, carbonates can sequester carbon over geologic time scales. This proposal investigates the use of coccolithophorids ? single-celled, marine algae that are the major global producers of calcium carbonate ? to sequester CO{sub 2} emissions from power plants. Cultivation of coccolithophorids for calcium carbonate (CaCO{sub 3}) precipitation is environmentally benign and results in a stable product with potential commercial value. Because this method of carbon sequestration does not impact natural ecosystem dynamics, it avoids controversial issues of public acceptability and legality associated with other options such as direct injection of CO{sub 2} into the sea and ocean fertilization. Consequently, cultivation of coccolithophorids could be carried out immediately and the amount of carbon sequestered as CaCO{sub 3} could be readily quantified. The significant advantages of this approach warrant its serious investigation. The major goals of the proposed research are to identify the growth conditions that will result in the maximum amount of CO{sub 2} sequestration through coccolithophorid calcite production and to evaluate the costs/benefits of using coccolithophorid cultivation ponds to abate CO{sub 2} emissions from power plants.

V. J. Fabry

2005-01-24T23:59:59.000Z

440

CALCIUM CARBONATE PRODUCTION BY COCCOLITHOPHORID ALGAE IN LONG TERM, CARBON DIOXIDE SEQUESTRATION  

SciTech Connect

Predictions of increasing levels of anthropogenic carbon dioxide (CO{sub 2}) and the specter of global warming have intensified research efforts to identify ways to sequester carbon. A number of novel avenues of research are being considered, including bioprocessing methods to promote and accelerate biosequestration of CO{sub 2} from the environment through the growth of organisms such as coccolithophorids, which are capable of sequestering CO{sub 2} relatively permanently. Calcium and magnesium carbonates are currently the only proven, long-term storage reservoirs for carbon. Whereas organic carbon is readily oxidized and releases CO{sub 2} through microbial decomposition on land and in the sea, carbonates can sequester carbon over geologic time scales. This proposal investigates the use of coccolithophorids single-celled, marine algae that are the major global producers of calcium carbonate to sequester CO{sub 2} emissions from power plants. Cultivation of coccolithophorids for calcium carbonate (CaCO{sub 3}) precipitation is environmentally benign and results in a stable product with potential commercial value. Because this method of carbon sequestration does not impact natural ecosystem dynamics, it avoids controversial issues of public acceptability and legality associated with other options such as direct injection of CO{sub 2} into the sea and ocean fertilization. Consequently, cultivation of coccolithophorids could be carried out immediately and the amount of carbon sequestered as CaCO{sub 3} could be readily quantified. The significant advantages of this approach warrant its serious investigation. The major goals of the proposed research are to identify the growth conditions that will result in the maximum amount of CO{sub 2} sequestration through coccolithophorid calcite production and to evaluate the costs/benefits of using coccolithophorid cultivation ponds to abate CO{sub 2} emissions from power plants.

V.J. Fabry

2001-07-01T23:59:59.000Z

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.


441

CALCIUM CARBONATE PRODUCTION BY COCCOLITHOPHORID ALGAE IN LONG TERM, CARBON DIOXIDE SEQUESTRATION  

SciTech Connect

Predictions of increasing levels of anthropogenic carbon dioxide (CO{sub 2}) and the specter of global warming have intensified research efforts to identify ways to sequester carbon. A number of novel avenues of research are being considered, including bioprocessing methods to promote and accelerate biosequestration of CO{sub 2} from the environment through the growth of organisms such as coccolithophorids, which are capable of sequestering CO{sub 2} relatively permanently. Calcium and magnesium carbonates are currently the only proven, long-term storage reservoirs for carbon. Whereas organic carbon is readily oxidized and releases CO{sub 2} through microbial decomposition on land and in the sea, carbonates can sequester carbon over geologic time scales. This proposal investigates the use of coccolithophorids--single-celled, marine algae that are the major global producers of calcium carbonate--to sequester CO{sub 2} emissions from power plants. Cultivation of coccolithophorids for calcium carbonate (CaCO{sub 3}) precipitation is environmentally benign and results in a stable product with potential commercial value. Because this method of carbon sequestration does not impact natural ecosystem dynamics, it avoids controversial issues of public acceptability and legality associated with other options such as direct injection of CO{sub 2} into the sea and ocean fertilization. Consequently, cultivation of coccolithophorids could be carried out immediately and the amount of carbon sequestered as CaCO{sub 3} could be readily quantified. The significant advantages of this approach warrant its serious investigation. The major goals of the proposed research are to identify the growth conditions that will result in the maximum amount of CO{sub 2} sequestration through coccolithophorid calcite production and to evaluate the costs/benefits of using coccolithophorid cultivation ponds to abate CO{sub 2} emissions from power plants.

V.J. Fabry, Ph.D.

2002-04-05T23:59:59.000Z

442

Property:Event/Organizer | Open Energy Information  

Open Energy Info (EERE)

Organizer Organizer Jump to: navigation, search Property Name Event/Organizer Property Type String Description The entity or entities responsible for organizing the event. This is typically a person or organization. More than one organizer can be attributed to each event. Pages using the property "Event/Organizer" Showing 25 pages using this property. (previous 25) (next 25) 1 11th Annual Workshop on Greenhouse Gas Emission Trading + International Energy Agency (IEA) + 11th Annual Workshop on Greenhouse Gas Emission Trading Day 2 + International Energy Agency (IEA) + 15th International Business Forum: Low Carbon High Growth - Business Models for a Changing Climate + German Agency for International Cooperation (GIZ) + 18th Africa Partnership Forum + African Partnership Forum +

443

Diverse Chemiresistors Based upon Covalently Modified Multiwalled Carbon Nanotubes  

E-Print Network (OSTI)

A diverse array of multiwalled carbon nanotube (MWCNT) sensory materials have been synthesized and used to create sensors capable of identifying volatile organic compounds (VOCs) on the basis of their functional groups. ...

Swager, Timothy Manning

444

Synthesis of Amides and Lactams in Supercritical Carbon Dioxide  

E-Print Network (OSTI)

Supercritical carbon dioxide can be employed as an environmentally friendly alternative to conventional organic solvents for the synthesis of a variety of carboxylic amides. The addition of amines to ketenes generated in ...

Mak, Xiao Yin

445

Glossary: Energy-Related Carbon Emissions  

U.S. Energy Information Administration (EIA)

Carbon Sequestration: The fixation of atmospheric carbon dioxide in a carbon sink through biological or physical processes. Carbon Sink: ...

446

Regional Carbon Sequestration Partnerships | Department of Energy  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Science & Innovation Carbon Capture and Storage Regional Carbon Sequestration Partnerships Regional Carbon Sequestration Partnerships DOE's Regional Carbon Sequestration...

447

Electron Microscopy of Carbon Nanotube Composites  

Science Conference Proceedings (OSTI)

Electron Microscopy of Carbon Nanotube Composites. Summary: Carbon nanomaterials such as carbon nanotubes (CNTs ...

2013-07-01T23:59:59.000Z

448

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

449

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

450

Microscale Quantification of the Absorption by Dissolved and Particulate Material in Coastal Waters with an ac-9  

Science Conference Proceedings (OSTI)

Measuring coastal and oceanic absorption coefficients of dissolved and particulate matter in the visible domain usually requires a methodology for amplifying the natural signal because conventional spectrophotometers lack the necessary ...

Michael S. Twardowski; James M. Sullivan; Percy L. Donaghay; J. Ronald V. Zaneveld

1999-06-01T23:59:59.000Z

451

Applicant Organization: | Department of Energy  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

Applicant Organization: Applicant Organization: Applicant Organization: More Documents & Publications BlueFire Ethanol, Inc. Applicant Organization: Applicant Organization:...

452

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

Science Conference Proceedings (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

453

A Low Carbon Economic Strategy for Scotland | Open Energy Information  

Open Energy Info (EERE)

Low Carbon Economic Strategy for Scotland Low Carbon Economic Strategy for Scotland Jump to: navigation, search Name A Low Carbon Economic Strategy for Scotland Agency/Company /Organization Government of Scotland Sector Energy, Land Topics Market analysis, Background analysis Website http://www.scotland.gov.uk/Res Country United Kingdom UN Region Western Europe References A Low Carbon Economic Strategy for Scotland[1] Abstract The Low Carbon Economic Strategy is an integral part of the Government's Economic Strategy (GES) to secure sustainable economic growth, and is a key component of our broader approach to meeting Scotland's climate change targets and securing the transition to a low carbon economy in Scotland "The Low Carbon Economic Strategy is an integral part of the Government's

454

Mexico-Low-Carbon Development | Open Energy Information  

Open Energy Info (EERE)

Mexico-Low-Carbon Development Mexico-Low-Carbon Development Jump to: navigation, search Logo: Mexico-ESMAP Low Carbon Growth Studies Program Name Mexico-ESMAP Low Carbon Growth Studies Program Agency/Company /Organization Energy Sector Management Assistance Program of the World Bank Sector Energy, Land Focus Area Energy Efficiency, Biomass, Industry, Forestry Topics GHG inventory, Low emission development planning, Policies/deployment programs, Background analysis Website http://www.esmap.org/filez/pub Country Mexico Central America References Low Carbon Development for Mexico[1] Abstract The Mexico study involves the preparation of a comprehensive package comprising: a low carbon strategy; the identification of priority sectors for carbon abatement; pre-feasibility level analysis of specific investment options; a country specific Marginal Abatement Cost (MAC) curve; identification of implementation barriers and necessary policy responses; and a prioritized list of potent...

455

International Carbon Storage Body Praises Department of Energy Projects |  

Energy.gov (U.S. Department of Energy (DOE)) Indexed Site

International Carbon Storage Body Praises Department of Energy International Carbon Storage Body Praises Department of Energy Projects International Carbon Storage Body Praises Department of Energy Projects November 8, 2012 - 12:00pm Addthis Washington, DC - Three U.S. Department of Energy (DOE) projects have been identified by an international carbon storage organization as an important advancement toward commercialization and large-scale deployment of carbon capture, utilization, and storage (CCUS) technologies. The projects were officially recognized by the Carbon Sequestration Leadership Forum (CSLF) at its recent meeting in Perth, Australia for making significant contributions to the development of global carbon dioxide (CO2) mitigation technologies. All three projects will appear in a yearly project portfolio on the CSLF website to keep the global community

456

Event:IETA Carbon Forum North America | Open Energy Information  

Open Energy Info (EERE)

IETA Carbon Forum North America IETA Carbon Forum North America Jump to: navigation, search Calendar.png IETA Carbon Forum North America: on 2012/10/01 "Carbon Forum North America -IETA's flagship North American event-will be one of the best opportunities of the year to network with the North American and global carbon markets, browse exhibits showcasing the work of leading companies, and learn what you need to know about this rapidly evolving space." Event Details Name IETA Carbon Forum North America Date 2012/10/01 Location District of Columbia Organizer International Emissions Trading Association Tags LEDS, training, CLEAN Website Event Website Ret LikeLike UnlikeLike You like this.Sign Up to see what your friends like. rieved from "http://en.openei.org/w/index.php?title=Event:IETA_Carbon_Forum_North_America&oldid=472

457

Nepal-Climate and Carbon Unit | Open Energy Information  

Open Energy Info (EERE)

Nepal-Climate and Carbon Unit Nepal-Climate and Carbon Unit (Redirected from SNV-Climate and Carbon Unit) Jump to: navigation, search Name SNV-Climate and Carbon Unit Agency/Company /Organization Netherlands Development Organisation, United Kingdom Department for International Development Sector Energy, Climate Topics Finance, Low emission development planning Website http://www.aepc.gov.np/index.p Country Nepal UN Region Eastern Asia References CCU[1] SNV-Climate and Carbon Unit Screenshot "In order to connect to this potential, SNV (Netherlands Development Organisation), the UK's Department for International Development (DFID/UKAID) and Government of Nepal have launched a Climate and Carbon Unit (CCU) within the Nepal Ministry of Environment's Alternative Energy Promotion Centre (AEPC). The CCU establishes climate change and carbon

458

Michael Heine, SGL Group - The Carbon Company, Carbon Fibers...  

NLE Websites -- All DOE Office Websites (Extended Search)

Carbon Fibers in Lightweight Systems for Wind Energy and Automotive Applications: Availability and Challenges for the Future Michael Heine, SGL Group - The Carbon Company, Carbon...

459

Carbon Efficiency, Carbon Reduction Potential, and Economic Developmen...  

Open Energy Info (EERE)

Carbon Reduction Potential, and Economic Development in the People's Republic of China Jump to: navigation, search Tool Summary Name: Carbon Efficiency, Carbon Reduction...

460

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