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1

Soil–Atmosphere Exchange of Nitrous Oxide, Nitric Oxide, Methane, and Carbon Dioxide in Logged and Undisturbed Forest in the Tapajos National Forest, Brazil  

Science Conference Proceedings (OSTI)

Selective logging is an extensive land use in the Brazilian Amazon region. The soil–atmosphere fluxes of nitrous oxide (N2O), nitric oxide (NO), methane (CH4), and carbon dioxide (CO2) are studied on two soil types (clay Oxisol and sandy loam ...

Michael Keller; Ruth Varner; Jadson D. Dias; Hudson Silva; Patrick Crill; Raimundo Cosme de Oliveira Jr.; Gregory P. Asner

2005-11-01T23:59:59.000Z

2

EIA - Greenhouse Gas Emissions - Nitrous Oxide Emissions  

Annual Energy Outlook 2012 (EIA)

nitrous oxide emisssions from industrial sources, 1990, 2005, 2008, and 2009 4.5. Waste management sources In 2009, treatment of residential and commercial wastewater produced 92...

3

EIA - Greenhouse Gas Emissions - Nitrous Oxide Emissions  

Gasoline and Diesel Fuel Update (EIA)

4. Nitrous Oxide Emissions 4. Nitrous Oxide Emissions 4.1 Total emissions U.S. nitrous oxide emissions in 2009 were 4 MMTCO2e (1.7 percent) below their 2008 total (Table 22). Sources of U.S. nitrous oxide emissions include agriculture, energy use, industrial processes, and waste management (Figure 22). The largest source is agriculture (73 percent), and the majority of agricultural emissions result from nitrogen fertilization of agricultural soils (87 percent of the agriculture total) and management of animal waste (13 percent). U.S. nitrous oxide emissions rose from 1990 to 1994, fell from 1994 to 2002, and returned to an upward trajectory from 2003 to 2007, largely as a result of increased use of synthetic fertilizers. Fertilizers are the primary contributor of emissions from nitrogen fertilization of soils, which grew by more than 30 percent from

4

Effect of fresh green waste and green waste compost on mineral nitrogen, nitrous oxide and carbon dioxide from a Vertisol  

Science Conference Proceedings (OSTI)

Incorporation of organic waste amendments to a horticultural soil, prior to expected risk periods, could immobilise mineral N, ultimately reducing nitrogen (N) losses as nitrous oxide (N{sub 2}O) and leaching. Two organic waste amendments were selected, a fresh green waste (FGW) and green waste compost (GWC) as they had suitable biochemical attributes to initiate N immobilisation into the microbial biomass and organic N forms. These characteristics include a high C:N ratio (FGW 44:1, GWC 35:1), low total N (14%). Both products were applied at 3 t C/ha to a high N (plus N fertiliser) or low N (no fertiliser addition) Vertisol soil in PVC columns. Cumulative N{sub 2}O production over the 28 day incubation from the control soil was 1.5 mg/N{sub 2}O/m{sup 2}, and 11 mg/N{sub 2}O/m{sup 2} from the control + N. The N{sub 2}O emission decreased with GWC addition (P < 0.05) for the high N soil, reducing cumulative N{sub 2}O emissions by 38% by the conclusion of the incubation. Analysis of mineral N concentrations at 7, 14 and 28 days identified that both FGW and GWC induced microbial immobilisation of N in the first 7 days of incubation regardless of whether the soil environment was initially high or low in N; with the FGW immobilising up to 30% of available N. It is likely that the reduced mineral N due to N immobilisation led to a reduced substrate for N{sub 2}O production during the first week of the trial, when soil N{sub 2}O emissions peaked. An additional finding was that FGW + N did not decrease cumulative N{sub 2}O emissions compared to the control + N, potentially due to the fact that it stimulated microbial respiration resulting in anaerobic micro sites in the soil and ultimately N{sub 2}O production via denitrification. Therefore, both materials could be used as post harvest amendments in horticulture to minimise N loss through nitrate-N leaching in the risk periods between crop rotations. The mature GWC has potential to reduce N{sub 2}O, an important greenhouse gas.

Vaughan, Sarah M., E-mail: s.vaughan@uq.edu.au [School of Land, Crop and Food Sciences, University of Queensland, St. Lucia, QLD 4072 (Australia); Dalal, Ram C. [School of Land, Crop and Food Sciences, University of Queensland, St. Lucia, QLD 4072 (Australia); Department of Environment and Resource Management, 80 Meiers Rd., Indooroopilly, QLD 4068 (Australia); Harper, Stephen M. [Department of Employment, Economic Development and Innovation, Warrego Highway, Gatton, QLD 4343 (Australia); Menzies, Neal W. [School of Land, Crop and Food Sciences, University of Queensland, St. Lucia, QLD 4072 (Australia)

2011-08-15T23:59:59.000Z

5

The biogeochemistry of marine nitrous oxide  

E-Print Network (OSTI)

Atmospheric nitrous oxide N?O concentrations have been rising steadily for the past century as a result of human activities. In particular, human perturbation of the nitrogen cycle has increased the N?O production rates ...

Frame, Caitlin H

2011-01-01T23:59:59.000Z

6

Low temperature plasma enhanced chemical vapor deposition of silicon oxide films using disilane and nitrous oxide  

Science Conference Proceedings (OSTI)

Keywords: disilane, low temperature, nitrous oxide, plasma enhanced chemical vapor deposition, silicon oxide

Juho Song; G. S. Lee; P. K. Ajmera

1995-10-01T23:59:59.000Z

7

Process Modeling of Global Soil Nitrous Oxide Emissions  

E-Print Network (OSTI)

Nitrous oxide is an important greenhouse gas and is a major ozone-depleting substance. To understand and

Saikawa, E.

2011-09-01T23:59:59.000Z

8

Spatiotemporal modelling in estimation of nitrous oxide emissions from soil.  

E-Print Network (OSTI)

??Nitrous oxide is a major greenhouse gas emission. The aim of this research was to develop and apply statistical models to characterize the complex spatial… (more)

Huang, Xiaodong

2013-01-01T23:59:59.000Z

9

EMISSIONS OF NITROUS OXIDE AND METHANE FROM CONVENTIONAL AND ALTERNATIVE FUEL MOTOR VEHICLES  

E-Print Network (OSTI)

EMISSIONS OF NITROUS OXIDE AND METHANE FROM CONVENTIONAL AND ALTERNATIVE FUEL MOTOR VEHICLES from motor vehicles because unlike emissions of CO2, which are relatively easy to estimate, emissions-related emissions. In the U.S., for example, emissions of carbon dioxide (CO2) from the production and use of motor

Kammen, Daniel M.

10

Methane and Nitrous Oxide: Their Effects on the Terrestrial Climate  

Science Conference Proceedings (OSTI)

Simplified band models are developed for methane (CH4) and nitrous oxide (N2O) bands in the longwave radiation spectrum. The band models are then employed in a radiation model to calculate the seasonally and latitudinally varying contributions of ...

L. Donner; V. Ramanathan

1980-01-01T23:59:59.000Z

11

On-farm Assessment of Nitrogen Fertilizer application to corn on Nitrous Oxide Emissions  

E-Print Network (OSTI)

mitigation of greenhouse gas emissions by agriculture. Nutr.1998. Nitrous oxide emission in three years as affected by2008. Soil-surface gas emissions. p.851-861. In: M.R. Carter

2009-01-01T23:59:59.000Z

12

A kinetics study of the atmospheric pressure CVD reaction of silane and nitrous oxide  

SciTech Connect

A mechanistic study of oxide deposition from silane and nitrous oxide between 495{sup 0}C and 690{sup 0}C was performed in a laminar flow, cool wall reactor. Results indicate the existence of two distinct chemical pathways. At high nitrous oxide concentrations, the deposition reaction is dominated by radical chain chemistry initiated by the decomposition of N/sub 2/O. At lower N/sub 2/O concentrations, the decomposition of silane to form silylene (SiH/sub 2/) initiates the deposition. Studies of the reaction of disilane and nitrous oxide confirmed the role of SiH/sub 2/ in the deposition. Reactions involving SiH/sub 2/ are used to explain the observed growth of sub-stoichiometric oxides under low N/sub 2/O conditions.

Chapple-Sokol, J.D.; Giunta, C.J.; Gordon, R.G. (Harvard Univ., Cambridge, MA (USA). Dept. of Chemistry)

1989-10-01T23:59:59.000Z

13

Modern Records of Atmospheric Nitrous Oxide (N2O) and a 2000-year Ice-core  

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

Modern Records of Atmospheric Nitrous Oxide (N2O) and a 2000-year Ice-core Modern Records of Atmospheric Nitrous Oxide (N2O) and a 2000-year Ice-core Record from Law Dome, Antarctica Introduction This page provides an introduction and links to records of atmospheric nitrous oxide (N2O) over the last 2000 years, emphasizing large data bases each representing currently active stations. Records in recent decades (time period depending on location) have been obtained from samples of ambient-air at remote locations, which represent changing global atmospheric conditions rather than influences of local sources. The longer (2000-year) record is from the Law Dome ice core in Antarctica. The ice-core record has been merged with modern annual data from Cape Grim, Tasmania to provide a 2000-year time series of annual values. A spline function has been fit to the data to provide a continuous time series of

14

Final Report for DOE grant no. DE-FG02-04ER63883: Can soil genomics predict the impact of precipitation on nitrous oxide flux from soil  

SciTech Connect

Nitrous oxide is a potent greenhouse gas that is released by microorganisms in soil. However, the production of nitrous oxide in soil is highly variable and difficult to predict. Future climate change may have large impacts on nitrous oxide release through alteration of precipitation patterns. We analyzed DNA extracted from soil in order to uncover relationships between microbial processes, abundance of particular DNA sequences and net nitrous oxide fluxes from soil. Denitrification, a microbial process in which nitrate is used as an electron acceptor, correlated with nitrous oxide flux from soil. The abundance of ammonia oxidizing archaea correlated positively, but weakly, with nitrous oxide production in soil. The abundance of bacterial genes in soil was negatively correlated with gross nitrogen mineralization rates and nitrous oxide release from soil. We suggest that the most important control over nitrous oxide production in soil is the growth and death of microorganisms. When organisms are growing nitrogen is incorporated into their biomass and nitrous oxide flux is low. In contrast, when microorganisms die, due to predation or infection by viruses, inorganic nitrogen is released into the soil resulting in nitrous oxide release. Higher rates of precipitation increase access to microorganisms by predators or viruses through filling large soil pores with water and therefore can lead to large releases of nitrous oxide from soil. We developed a new technique, stable isotope probing with 18O-water, to study growth and mortality of microorganisms in soil.

Egbert Schwartz

2008-12-15T23:59:59.000Z

15

Nitrous oxide (N?O) isotopic composition in the troposphere : instrumentation, observations at Mace Head, Ireland, and regional modeling  

E-Print Network (OSTI)

Nitrous oxide (N?O) is a significant greenhouse gas and main contributor to stratospheric ozone destruction. Surface measurements of N?O mole fractions have been used to attribute source and sink strengths, but large ...

Potter, Katherine Ellison

2011-01-01T23:59:59.000Z

16

Vibrational Infrared Lifetime of the Anesthetic nitrous oxide gas in solution  

E-Print Network (OSTI)

The lifetime of the asymmetric fundamental stretching 2218 cm$^{-1}$ vibration of the anesthetic gas nitrous oxide (N$_2$O) dissolved in octanol and olive oil is reported. These solvents are model systems commonly used to assess anesthetic potency. Picosecond time-scale molecular dynamics simulations have suggested that protein dynamics or membrane dynamics play a role in the molecular mechanism of anesthetic action. Ultrafast infrared spectroscopy with 100 fs time resolution is an ideal tool to probe dynamics of anesthetic molecules on such timescales. Pump-probe studies at the peak of the vibrational band yield a lifetime of $55 \\pm 1$ ps in olive oil and $52 \\pm 1 ps$ in octanol. The similarity of lifetimes suggests that energy relaxation of the anesthetic is determined primarily by the hydrophobic nature of the environment, consistent with models of anesthetic action. The results show that nitrous oxide is a good model system for probing anesthetic-solvent interactions using nonlinear infrared spectroscop...

Chieffo, Logan; Shattuck, Jeffrey; Hong, Mi K; Ziegler, Lawrence; Erramilli, Shyamsunder

2006-01-01T23:59:59.000Z

17

Nitrous oxide production from radiolysis of simulted high-level nuclear waste solutions  

DOE Green Energy (OSTI)

Nitrous oxide gas (N{sub 2}O) is produced by the radiolysis of aqueous nitrate or nitrite solutions in the presence of organic compounds. When ethylenediaminetetraacetic acid (EDTA) or N- (2-hydroxyethyl)-ethylenediaminetriacetic acid (HEDTA) is present, the G-value for hydrogen increases and N{sub 2}O become the major gaseous product (G=0.54). A survey of organic compounds indicates the amount of N{sub 2}O formed depends on the structure of the organic. With highly oxidized organics (carbonate, formate, acetate and oxalate), little or no N{sub 2}O is formed. Aromatic and aliphatic organics (sodium tetraphenylborate, benzene, phenol, n-paraffin, and tributylphosphate) produce small amounts of N{sub 2}O. Water soluble, easily oxidized organics (methanol, ethanol, isopropanol, n-butanol, acetone, and ethylene glycol) produce large amounts of N{sub 2}O relative to the previous two categories. Nitrous oxide production is not greatly affected by pH between neutral and pH=13, but increases significantly in acid solution. The G-value for N{sub 2}O production in 10 wt% potassium tetraphenylborate slurries has been measured under process conditions important at the Savannah River Site.

Walker, D.D.; Hobbs, D.T.; Tiffany, J.B.; Bibler, N.E. [Westinghouse Savannah River Co., Aiken, SC (United States); Meisel, D. [Argonne National Lab., IL (United States)

1992-07-01T23:59:59.000Z

18

Nitrous oxide production from radiolysis of simulted high-level nuclear waste solutions  

DOE Green Energy (OSTI)

Nitrous oxide gas (N{sub 2}O) is produced by the radiolysis of aqueous nitrate or nitrite solutions in the presence of organic compounds. When ethylenediaminetetraacetic acid (EDTA) or N- (2-hydroxyethyl)-ethylenediaminetriacetic acid (HEDTA) is present, the G-value for hydrogen increases and N{sub 2}O become the major gaseous product (G=0.54). A survey of organic compounds indicates the amount of N{sub 2}O formed depends on the structure of the organic. With highly oxidized organics (carbonate, formate, acetate and oxalate), little or no N{sub 2}O is formed. Aromatic and aliphatic organics (sodium tetraphenylborate, benzene, phenol, n-paraffin, and tributylphosphate) produce small amounts of N{sub 2}O. Water soluble, easily oxidized organics (methanol, ethanol, isopropanol, n-butanol, acetone, and ethylene glycol) produce large amounts of N{sub 2}O relative to the previous two categories. Nitrous oxide production is not greatly affected by pH between neutral and pH=13, but increases significantly in acid solution. The G-value for N{sub 2}O production in 10 wt% potassium tetraphenylborate slurries has been measured under process conditions important at the Savannah River Site.

Walker, D.D.; Hobbs, D.T.; Tiffany, J.B.; Bibler, N.E. (Westinghouse Savannah River Co., Aiken, SC (United States)); Meisel, D. (Argonne National Lab., IL (United States))

1992-01-01T23:59:59.000Z

19

Developing Greenhouse Gas Emissions Offsets by Reducing Nitrous Oxide (N2O) Emissions in Agricultural Crop Production  

Science Conference Proceedings (OSTI)

This final project report describes a three-year long EPRI supplemental project entitled "Developing Greenhouse Gas Emissions Offsets by Reducing Nitrous Oxide (N2O) Emissions." This EPRI-sponsored project investigated an innovative approach to developing large-scale, cost-effective greenhouse gas (GHG) emissions offsets that potentially can be implemented across broad geographic areas of the United States and internationally.

2009-12-17T23:59:59.000Z

20

Developing Greenhouse Gas Emissions Offsets by Reducing Nitrous Oxide (N2O) Emissions in Agricultural Crop Production  

Science Conference Proceedings (OSTI)

This Technical Update covers the first year of a three-year-long EPRI research project entitled Developing Greenhouse Gas Emissions Offsets by Reducing Nitrous Oxide (N2O) Emissions in Agricultural Crop Production. The report provides a project overview and explains the preliminary results yielded from the first year of on-farm research.

2007-10-30T23:59:59.000Z

Note: This page contains sample records for the topic "dioxide nitrous oxide" 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

Developing Greenhouse Gas Emissions Offsets by Reducing Nitrous Oxide (N2O) Emissions in Agricultural Crop Production  

Science Conference Proceedings (OSTI)

This report covers the first two years of a three-year long project entitled "Developing Greenhouse Gas Emissions Offsets by Reducing Nitrous Oxide (N2O) Emissions." This EPRI-sponsored project is investigating an innovative approach to developing large-scale and potentially cost-effective greenhouse gas (GHG) emissions offsets that could be implemented across broad geographic areas of the U.S. and internationally. The tools and information developed in this project will broaden the GHG emissions offset ...

2008-11-11T23:59:59.000Z

22

Regional Sources of Nitrous Oxide over the United States: Seasonal Variation and Spatial Distribution  

SciTech Connect

This paper presents top-down constraints on the magnitude, spatial distribution, and seasonality of nitrous oxide (N{sub 2}O) emissions over the central United States. We analyze data from tall towers in 2004 and 2008 using a high resolution Lagrangian particle dispersion model paired with both geostatistical and Bayesian inversions. Our results indicate peak N{sub 2}O emissions in June with a strong seasonal cycle. The spatial distribution of sources closely mirrors data on fertilizer application with particularly large N{sub 2}O sources over the US Cornbelt. Existing inventories for N{sub 2}O predict emissions that differ substantially from the inverse model results in both seasonal cycle and magnitude. We estimate a total annual N{sub 2}O budget over the central US of 0.9-1.2 TgN/yr and an extrapolated budget for the entire US and Canada of 2.1-2.6 TgN/yr. By this estimate, the US and Canada account for 12-15% of the total global N{sub 2}O source or 32-39% of the global anthropogenic source as reported by the Intergovernmental Panel on Climate Change in 2007.

Miller, S. M.; Kort, E. A.; Hirsch, A. I.; Dlugokencky, E. J.; Andrews, A. E.; Xu, X.; Tian, H.; Nehrkorn, T.; Eluszkiewicz, J.; Michalak, A. M.; Wofsy, S. C.

2012-01-01T23:59:59.000Z

23

Developing Greenhouse Gas Emissions Offsets by Reducing Nitrous Oxide (N2O) Emissions in Agricultural Crop Production: Experience Validating a New GHG Offset Protocol  

Science Conference Proceedings (OSTI)

This project report describes in part the second phase (years four through six, 2010–2012) of a two-phase, six-year long EPRI-sponsored research project entitled “Developing Greenhouse Gas Emissions Offsets by Reducing Nitrous Oxide (N2O) Emissions.” This project investigated an innovative approach to developing large-scale, cost-effective greenhouse gas (GHG) emissions offsets that potentially can be implemented across broad geographic areas of the ...

2013-05-28T23:59:59.000Z

24

Nitrogen Fertilizer Management for Nitrous Oxide (N2O) Mitigation in Intensive Corn (Maize) Production: An Emissions Reduction Proto col for US Midwest Agriculture  

Science Conference Proceedings (OSTI)

Status: Published Citation: Millar, N; Robertson, GP; Grace, PR; Gehl, RJ; and Hoben, JP. 2010. Nitrogen Fertilizer Management for Nitrous Oxide (N2O) Mitigation in Intensive Corn (Maize) Production: An Emissions Reduction Protocol for US Midwest Agriculture. In Journal of Mitigation and Adaptation Strategies for Global Change,Volume 15, Number 2, 2010, pp. 185-204. Link to Journal Publication: See Journal of Mitigation and Adaptation Strategies for Global Change.

2010-09-03T23:59:59.000Z

25

Nitrogen Fertilizer Management for Nitrous Oxide (N2O) Mitigation in Intensive Corn (Maize) Production: An Emissions Redu ction Protocol for U.S. Midwest Agriculture  

Science Conference Proceedings (OSTI)

Status: Published Citation: Millar, N; Robertson, GP; Grace, PR; Gehl, RJ; and Hoben; JP. 2010. Nitrogen Fertilizer Management for Nitrous Oxide (N2O) Mitigation in Intensive Corn (Maize) Production: An Emissions Reduction Protocol for U.S. Midwest Agriculture. In Mitigation and Adaptation Strategies for Global Change, Volume 15, Number 2, 2010, pp. 185-204. A peer-reviewed journal article that identifies, describes and analyzes socio-economic factors that may encourage or inhibit farmers from participat...

2009-12-17T23:59:59.000Z

26

Zinc-catalyzed copolymerization of carbon dioxide and propylene oxide  

E-Print Network (OSTI)

The zinc-catalyzed copolymerization of carbon dioxide and propylene oxide, which is one of the promising reactions for the utilization of carbon dioxide, has been investigated from various aspects. Above all, considering that supercritical carbon dioxide has recently been paid attention in the field of extraction, separation, and reaction medium, its aptitude for both a reaction solvent and a reactant was examined in zinc glutarate-catalyzed reactions. As a result, it was proved that supercritical carbon dioxide was a suitable substitute for organic solvents in the copolymerization reactions. Great diffusivity of supercritical carbon dioxide into polymer segments was thought to promote carbon dioxide supply to the active sites of the zinc species and to afford alternating polycarbonate production. Low reaction temperature appeared to be advantageous to polycarbonate and cyclic carbonate formation. Apart from zinc glutarate catalyst whose detailed mechanistic studies were hard to perform due to its insolubility, some other zinc compounds were studied. A homogeneous catalyst, bis(ethyl fumarato)zinc, showed similar polycarbonate yield to zinc glutarate, and the method of the catalyst preparation affected its catalytic activity. Only a small amount of the catalyst was considered to be active in the copolymerization process even in the homogeneous systems. In the zinc dicarboxylate complexes, the carbon number between two carboxyl groups and the steric nature in the vicinity of the zinc atom might be important factors for the copolymerization catalysis.

Katsurao, Takumi

1994-01-01T23:59:59.000Z

27

Thermal and combined thermal and radiolytic reactions involving nitrous oxide, hydrogen, nitrogen, and ammonia in contact with tank 241-SY-101 simulated waste  

DOE Green Energy (OSTI)

Work described in this report was conducted at Pacific Northwest National Laboratory (PNNL) for the Flammable Gas Safety Project, the purpose of which is to develop information needed to support Westinghouse Hanford Company (WHC) in their efforts to ensure the safe interim storage of wastes at the Hanford Site. Described in this report are the results of tests to evaluate the rates of thermal and combined thermal and radiolytic reactions involving flammable gases in the presence of Tank 241-SY-101 simulated waste. Flammable gases generated by the radiolysis of water and by the thermal and radiolytic decomposition of organic waste constituents may themselves participate in further reactions. Examples include the decomposition of nitrous oxide to yield nitrogen and oxygen, the reaction of nitrous oxide and hydrogen to produce nitrogen and water, and the reaction of nitrogen and hydrogen to produce ammonia. The composition of the gases trapped in bubbles in the wastes might therefore change continuously as a function of the time that the gas bubbles are retained.

Bryan, S.A.; Pederson, L.R.

1996-02-01T23:59:59.000Z

28

Nitrous oxide emissions  

SciTech Connect

The purpose of this paper is to report the effect of key operating parameters, the relative importance of coal type, and the potentially significant coal properties for producing N{sub 2}O emissions in an atmospheric circulating fluidized-bed combustor (CFBC) and pressurized bubbling fluidized-bed combustor (PFBC). The generation of N{sub 2}O emissions is quantified in an empirical model based on the experimental data.

Mann, M.D.; Collings, M.E.; Young, B.C.

1992-12-01T23:59:59.000Z

29

Nitrous oxide emissions  

SciTech Connect

The purpose of this paper is to report the effect of key operating parameters, the relative importance of coal type, and the potentially significant coal properties for producing N[sub 2]O emissions in an atmospheric circulating fluidized-bed combustor (CFBC) and pressurized bubbling fluidized-bed combustor (PFBC). The generation of N[sub 2]O emissions is quantified in an empirical model based on the experimental data.

Mann, M.D.; Collings, M.E.; Young, B.C.

1992-01-01T23:59:59.000Z

30

Bayesian Modelling Volatility of Growth Rate in Atmospheric Carbon Dioxide Concentrations  

Science Conference Proceedings (OSTI)

Atmospheric gases, such as carbon dioxide, ozone, methane, nitrous oxide, and etc., create a natural greenhouse effect and cause climate change. Therefore, modelling behavior of these gases could help policy makers to control greenhouse effects. In a ... Keywords: Stochastic volatility, Smooth transition autoregressive, Markov chain Monte Carlo, methods, Bayesian, ARCH, GARCH

Esmail Amiri

2009-12-01T23:59:59.000Z

31

Standard test methods for analysis of sintered gadolinium oxide-uranium dioxide pellets  

E-Print Network (OSTI)

1.1 These test methods cover procedures for the analysis of sintered gadolinium oxide-uranium dioxide pellets to determine compliance with specifications. 1.2 The analytical procedures appear in the following order: Section Carbon (Total) by Direct CombustionThermal Conductivity Method C1408 Test Method for Carbon (Total) in Uranium Oxide Powders and Pellets By Direct Combustion-Infrared Detection Method Chlorine and Fluorine by Pyrohydrolysis Ion-Selective Electrode Method C1502 Test Method for Determination of Total Chlorine and Fluorine in Uranium Dioxide and Gadolinium Oxide Gadolinia Content by Energy-Dispersive X-Ray Spectrometry C1456 Test Method for Determination of Uranium or Gadolinium, or Both, in Gadolinium Oxide-Uranium Oxide Pellets or by X-Ray Fluorescence (XRF) Hydrogen by Inert Gas Fusion C1457 Test Method for Determination of Total Hydrogen Content of Uranium Oxide Powders and Pellets by Carrier Gas Extraction Isotopic Uranium Composition by Multiple-Filament Surface-Ioni...

American Society for Testing and Materials. Philadelphia

2006-01-01T23:59:59.000Z

32

structural defects in uranium dioxide : from oxidation to irradiation.  

Science Conference Proceedings (OSTI)

About this Abstract. Meeting, 2014 TMS Annual Meeting & Exhibition. Symposium , Radiation Effects in Oxide Ceramics and Novel LWR Fuels. Presentation Title ...

33

Oxygen Pathways and Carbon Dioxide Utilization in Methane Partial Oxidation in Ambient Temperature  

E-Print Network (OSTI)

- ronmental impact. Present technology uses steam reforming to produce synthesis gas which is converted into enhance- ment of the carbon balance of methane conversion by reforming with CO2 in order to "recycleOxygen Pathways and Carbon Dioxide Utilization in Methane Partial Oxidation in Ambient Temperature

Mallinson, Richard

34

On the Ratio of Sulfur Dioxide to Nitrogen Oxides as an Indicator of Air Pollution Sources  

Science Conference Proceedings (OSTI)

The ratio of sulfur dioxide to nitrogen oxides (RSN = SO2/NOx) is one indicator of air pollution sources. The role of this ratio in source attribution is illustrated here for the Ashdod area, located in the southern coastal plain of Israel. The ...

Ronit Nirel; Uri Dayan

2001-07-01T23:59:59.000Z

35

Improved efficiency in the sulfur dioxide-iodine hydrogen cycle through the use of magnesium oxide  

DOE Green Energy (OSTI)

The reaction of iodine with dry magnesium oxide and magnesium sulfite hexahydrate was studied experimentally as a possible means of improving the efficiency of the sulfur dioxide-iodine cycle. When no extra water was introduced, the maximum product yield was 67% obtained at 423 K. With excess water vapor, a nonporous plug was formed which prevented complete reaction. In the second case, maximum yield was 62% measured at 433 K showing that added water does not increase reaction products. This reaction gives an alternate route for producing hydrogen from water via the sulfur dioxide-iodine process.

Mason, C.F.V.; Bowman, M.G.

1981-01-01T23:59:59.000Z

36

CARBON DIOXIDE UPTAKE STUDIES IN ALGAE GROWN IN WATER AND DEUTERIUM OXIDE  

SciTech Connect

A procedure is described for studying carbon dioxide uptake in algae using C/sup 14/-labeled sodium bicarbonate as the source of carbon dioxide, Actively dividing, water grown and deuterium oxide adapted, Scenedesmus obliquus and Chlorella vulgaris were employed in the studies. Uptake comparisons were made over pH range 6 to 9 using appropriate buffer systems. Uptake was fairly constant in the range pH 6 to 8 for both the aqueous and deuterated algae. Above pH 8 uptake dropped markedly. In general, the deuterated algae showed between 1O and 30% lower uptake than ordinary algae. Greater chlorophyll content is associated with higher carbon dioxide uptake. (auth)

Blake, M.I.; Kaganove, A.S.; Katz, J.J.

1962-04-01T23:59:59.000Z

37

Solar Thermo-Chemical Splitting of Carbon Dioxide by Metal Oxide ...  

Science Conference Proceedings (OSTI)

Presentation Title, Solar Thermo-Chemical Splitting of Carbon Dioxide by Metal ... which can split carbon dioxide as well as water molecules by abstracting ...

38

Analysis of Strategies for Reducing Multiple Emissions from Electric Power Plants: Sulfur Dioxide, Nitrogen Oxides, Carbon Dioxide, and Mercury and a Renewable Portfolio Standard  

Gasoline and Diesel Fuel Update (EIA)

3 3 ERRATA Analysis of Strategies for Reducing Multiple Emissions from Electric Power Plants: Sulfur Dioxide, Nitrogen Oxides, Carbon Dioxide, and Mercury and a Renewable Portfolio Standard July 2001 Energy Information Administration Office of Integrated Analysis and Forecasting U.S. Department of Energy Washington, DC 20585 This Service Report was prepared by the Energy Information Administration, the independent statistical and analytical agency within the Department of Energy. The information contained herein should be attributed to the Contacts This report was prepared by the Office of Integrated Analysis and Forecasting, Energy Information Adminis- tration. General questions concerning the report may be directed to Mary J. Hutzler (202/586-2222, mhutzler @eia.doe.gov), Director of the Office of Integrated Analysis and Forecasting, Scott B. Sitzer (202/586-2308,

39

MINIMIZING NET CARBON DIOXIDE EMISSIONS BY OXIDATIVE CO-PYROLYSIS OF COAL/BIOMASS BLENDS  

DOE Green Energy (OSTI)

Solid fuels vary significantly with respect to the amount of CO{sub 2} directly produced per unit heating value. Elemental carbon is notably worse than other solid fuels in this regard, and since carbon (char) is an intermediate product of the combustion of almost all solid fuels, there is an opportunity to reduce specific CO{sub 2} emissions by reconfiguring processes to avoid char combustion wholly or in part. The primary goal of this one-year Innovative Concepts project is to make a fundamental thermodynamic assessment of three modes of solid fuel use: (1) combustion, (2) carbonization, and (3) oxidative pyrolysis, for a wide range of coal and alternative solid fuels. This period a large set of thermodynamic calculations were carried out to assess the potential of the three processes. The results show that the net carbon dioxide emissions and the relative ranking of the different processes depends greatly on the particular baseline fossil fuel being displaced by the new technology. As an example, in a baseline natural gas environment, it is thermodynamically more advantageous to carbonize biomass than to combust it, and even more advantageous to oxidatively pyrolyze the biomass.

Robert Hurt; Todd Lang

2001-06-25T23:59:59.000Z

40

PROCESSING OF HIGH-FIRED URANIUM DIOXIDE FUELS BY A REDUCTION-MERCURY EXTRACTION-OXIDATION PROCESS  

DOE Green Energy (OSTI)

A preliminary flowsheet for the purification of uranium dioxide fuels by a magnesium reduction-- mercury extraction-- steam oxidation process is proposed. Feasibility was indicated by laboratory-scale scouting experiments. Data evaluation indicated 100% reduction of uranium dioxide by magnesium although this figure was not demonstrated, chiefly because of poor choice of materials and design of equipment. Steam oxidation of uranlum tetramercuride produced an oxide with an O/U ratio of 2.43. This ratio was decreased to 2.09 by heating the oxide in a hydrogen atmosphere at 900 deg C for 1 hr. The final product had a surface area of 3.5 m/sup 2//g, and 18% of the panticles were < 1 mu diam. A pellet of the oxide sintered at 1750 deg C had a density of 9.76 g/cc, 89% of theoretical. Decontamination factors demonstrated for ruthenium, cesium, and samarium, when present originally in amounts equivalent to 30,000 Mwd/ton fuel burnup and 60 days' decay, were

Messing, A. F.; Dean, O. C.

1960-08-12T23:59:59.000Z

Note: This page contains sample records for the topic "dioxide nitrous oxide" 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

Selective methane oxidation over promoted oxide catalysts. Quarterly report, September 1 - November 30, 1995  

DOE Green Energy (OSTI)

The objective of this research is the selective oxidation of methane to C{sub 2}H{sub 4} hydrocarbons and to oxygenates, in particular formaldehyde and methanol. Air, oxygen, or carbon dioxide rather than nitrous oxide, are utilized as the oxidizing gas at high gas hourly space velocity but mild reaction conditions (500-700{degrees}C, 1 atm total pressure). All the investigated processes are catalytic, aiming at minimizing gas phase reactions that are difficult to control. During this quarter, solid state {sup 51}V NMR and double catalyst bed experiments were conducted to demonstrate the unfavorable effect of the presence of bulk crystalline V{sub 2}O{sub 5} in V{sub 2}O{sub 5}-SiO{sub 2} xerogel catalysts on selective oxidation of methane to methanol and formaldehyde. Results are discussed.

Klier, Kamil; Herman, R.G.; Wang, C.B. [USDOE Morgantown Energy Technology Center, WV (United States)

1995-12-31T23:59:59.000Z

42

Atmospheric Trace Gases, Carbon Isotopes, Radionuclides, and Aerosols: Atmospheric Carbon Dioxide Data from the Carbon Dioxide Information Analysis Center (CDIAC)  

DOE Data Explorer (OSTI)

CDIAC products include numeric data packages, publications, trend data, atlases, models, etc. and can be searched for by subject area, keywords, authors, product numbers, time periods, collection sites, spatial references, etc. Some of the collections may also be included in the CDIAC publication titled Trends Online: A Compendium of Global Change Data. Most datasets, many with numerous data files, are free to download from CDIAC's ftp area. Information related to atmospheric carbon dioxide data includes: Atmospheric Carbon Dioxide and Carbon Isotopes • Atmospheric carbon dioxide records from Mauna Loa, Hawaii • Monthly atmospheric CO2 mixing ratios and other data from the NOAA/CMDL continuous monitoring network • Data from the CSIRO GASLAB Flask Sampling Network • Atmospheric CO2 records from continuous measurements at Jubany Station, Antarctica and from 10 sites in the SIO air sampling network • Historical data from the extended Vostok ice core (2003) and the Siple Station ice core (1997) • Historical records from the Law Dome DE08, DE08-2, and DSS ice cores (1998) • AmeriFlux Carbon Dioxide, Water Vapor, and Energy Balance Measurements • Data from the Canadian Background Air Pollution Monitoring Network • Flask Samples from at U.S.S.R.-Operated Sites (1991) • The CISIRO (Australia) Monitoring Program from Aircraft for 1972-1981 • CO2 Concentrations in Surface Water and the Atmosphere during 1986-1989 NOAA/PMEL Cruises in the Pacific and Indian Oceans • Surface Water and Atmospheric CO2 and Nitrous Oxide Observations by Shipboard Automated Gas Chromatography: Results from Expeditions Between 1977 and 1990 (1992) • IPCC Working Group 1, 1994: Modeling Results Relating Future Atmospheric CO2 Concentrations to Industrial Emissions (1995). New datasets are added when available to the category of atmospheric carbon dioxide.

43

REDUCTION AND SEQUESTRATION OF PERTECHNETATE TO TECHNETIUM DIOXIDE AND PROTECTION FROM RE-OXIDATION  

Science Conference Proceedings (OSTI)

This effort is part of the technetium management initiative and provides data for the handling and disposition of technetium. To that end, the objective of this effort was to challenge tin(II)apatite (Sn(II)apatite) against double-shell tank 241-AN-I0S simulant spiked with pertechnetate (TcO{sub 4}{sup -}). The Sn(II)apatite used in this effort was synthesized on site using a recipe developed at and provided by Sandia National Laboratories; the synthesis provides a high quality product while requiring minimal laboratory effort. The Sn(II)apatite reduces pertechnetate from the mobile +7 oxidation state to the non-mobile +4 oxidation state. It also sequesters the technetium and does not allow for re-oxidization to the mobile +7 state under acidic or oxygenated conditions within the tested period of time (6 weeks). Previous work indicated that the Sn(II)apatite can achieve an ANSI leachability index in Cast Stone of 12.8. The technetium distribution coefficient for Sn(II)apatite exhibits a direct correlation with the pH of the contaminated media. Table 1 shows Sn(II)apatite distribution coefficients as a function of pH. The asterisked numbers indicate that the lower detection limit of the analytical instrument was used to calculate the distribution coefficient as the concentration of technetium left in solution was less than the detection limit.

DUNCAN JB; JOHNSON JM; MOORE WP; HAGERTY KJ; RHODES RN; MOORE RC

2012-07-11T23:59:59.000Z

44

THE HIGH TEMPERATURE BEHAVIOR OF METALLIC INCLUSIONS IN URANIUM DIOXIDE.  

E-Print Network (OSTI)

Products in Irradiated Uranium Dioxide," UKAEA Report AERE-OF METALLIC INCLUSIONS IN URANIUM DIOXIDE Rosa Lu Yang (Chemical State of Irradiated Uranium- Plutonium Oxide Fuel

Yang, Rosa Lu.

2010-01-01T23:59:59.000Z

45

Sulfur isotope fractionation during oxidation of sulfur dioxide: gas-phase oxidation by OH radicals and aqueous oxidation by H2O2, O3 and iron catalysis  

E-Print Network (OSTI)

The oxidation of SO[subscript 2] to sulfate is a key reaction in determining the role of sulfate in the environment through its effect on aerosol size distribution and composition. Sulfur isotope analysis has been used to ...

Harris, E.

46

Technology Innovation Program Transforming America's ...  

Science Conference Proceedings (OSTI)

... Reducing US dependence on foreign oil. # Reducing carbon dioxide, nitrous oxide, and other ... Separation, sequestration, and utilization of CO2 ...

2011-02-02T23:59:59.000Z

47

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

48

Standard specification for blended uranium oxides with 235U content of less than 5 % for direct hydrogen reduction to nuclear grade uranium dioxide  

E-Print Network (OSTI)

1.1 This specification covers blended uranium trioxide (UO3), U3O8, or mixtures of the two, powders that are intended for conversion into a sinterable uranium dioxide (UO2) powder by means of a direct reduction process. The UO2 powder product of the reduction process must meet the requirements of Specification C 753 and be suitable for subsequent UO2 pellet fabrication by pressing and sintering methods. This specification applies to uranium oxides with a 235U enrichment less than 5 %. 1.2 This specification includes chemical, physical, and test method requirements for uranium oxide powders as they relate to the suitability of the powder for storage, transportation, and direct reduction to UO2 powder. This specification is applicable to uranium oxide powders for such use from any source. 1.3 The scope of this specification does not comprehensively cover all provisions for preventing criticality accidents, for health and safety, or for shipping. Observance of this specification does not relieve the user of th...

American Society for Testing and Materials. Philadelphia

2001-01-01T23:59:59.000Z

49

Building Energy Software Tools Directory: EMISS  

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

Three types of emission factors are currently included: carbon dioxide, sulfur dioxide, nitrous oxide. Emissions factors are specified separately for six different end-use...

50

Biomass burning sources of nitrogen oxides, carbon monoxide, and non-methane hydrocarbons  

SciTech Connect

Biomass burning is an important source of many key tropospheric species, including aerosols, carbon dioxide (CO{sub 2}), nitrogen oxides (NO{sub {times}}=NO+NO{sub 2}), carbon monoxide (CO), methane (CH{sub 4}), nitrous oxide (N{sub 2}O), methyl bromide (CH{sub 3}Br), ammonia (NH{sub 3}), non-methane hydrocarbons (NMHCs) and other species. These emissions and their subsequent products act as pollutants and affect greenhouse warming of the atmosphere. One important by-product of biomass burning is tropospheric ozone, which is a pollutant that also absorbs infrared radiation. Ozone is formed when CO, CH{sub 4}, and NMHCs react in the presence of NO{sub {times}} and sunlight. Ozone concentrations in tropical regions (where the bulk of biomass burning occurs) may increase due to biomass burning. Additionally, biomass burning can increase the concentration of nitric acid (HNO{sub 3}), a key component of acid rain.

Atherton, C.S.

1995-11-01T23:59:59.000Z

51

Selective methane oxidation over promoted oxide catalysts. Quarterly report, March--May 1995  

DOE Green Energy (OSTI)

The objective of this research is the selective oxidative coupling of methane to C{sub 2}H{sub 4} hydrocarbons and oxygenates, in particular formaldehyde and methanol. Air, oxygen or carbon dioxide, rather than nitrous oxide will be utilized as the oxidizing gas at high gas hourly space velocity, but mild reaction conditions (500-700 {degrees}C, 1 atm total pressure). All the investigated processes are catalytic, aiming at minimizing gas phase reactions that are difficult to control. The research is divided into the following three tasks: (1) maximizing selective methane oxidation to C{sub 2}H{sub 4} products over promoted Sr/La{sub 2}O{sub 3}; (2) selective methane oxidation to oxygenates; and (3) catalyst characterization and optimization. Task 1 dealt with the preparation, testing, and optimization of acidic promoted lanthana-based catalysts for the synthesis of C{sub 2}H{sub 4} hydrocarbons and is essentially completed. Task 2 aims at the formation and optimization of promoted catalysts for the synthesis of oxygenates, in particular formaldehyde and methanol. Task 3 involves characterization of the most promising catalysts so that optimization can be achieved under Task 2. Accomplishments for this period are presented.

Klier, K.; Herman, R.G.; Wang, Chaun-Bao; Shi, Chunlei; Sun, Qun

1995-08-01T23:59:59.000Z

52

Premixed Carbon Monoxide–Nitrous Oxide–Hydrogen Flames ...  

Science Conference Proceedings (OSTI)

... the combustion emission charac- teristics of stationary and mobile power plants. ... present data are in good agreement with the low-hydro- gen data ...

2012-12-06T23:59:59.000Z

53

Three Dimensional CFD Model of a Planar Solid Oxide Electrolysis Cell for Co-Electrolysis of Steam and Carbon-Dioxide  

SciTech Connect

A three-dimensional computational fluid dynamics (CFD) model has been created to model high temperature co-electrolysis of steam and carbon dioxide in a planar solid oxide electrolyzer (SOE). A research program is under way at the Idaho National Laboratory (INL) to simultaneously address the research and scale-up issues associated with the implementation of planar solid-oxide electrolysis cell technology for syn-gas production from CO2 and steam. Various runs have been performed under different run conditions to help assess the performance of the SOE. An experimental study is also being performed at the INL to assess the SOE. Model results provide detailed profiles of temperature, Nernst potential, operating potential, anode-side gas composition, cathode-side gas composition, current density and syn-gas production over a range of stack operating conditions. Typical results of current density versus cell potential, cell current versus H2 and CO production, temperature, and voltage potential are all presented within this paper. Plots of mole fraction of CO2, CO, H2, H2O, O2, are presented. Currently there is strong interest in the large-scale production of syn-gas from CO2 and steam to be reformed into a usable transportation fuel. This process takes the carbon-neutral approach where the amount of CO2 in the atmosphere does not increase. Consequently, there is a high level of interest in production of syn-gas from CO2 and steam electrolysis. Worldwide, the demand for light hydrocarbon fuels like gasoline and diesel oil is increasing. To satisfy this demand, oil companies have begun to utilize oil deposits of lower hydrogen. In the mean time, with the price of oil currently over $70 / barrel, synthetically-derived hydrocarbon fuels (synfuels) have become economical. Synfuels are typically produced from syngas – hydrogen (H2) and carbon monoxide (CO) -- using the Fischer-Tropsch process, discovered by Germany before World War II. South Africa has used synfuels to power a significant number of their buses, trucks, and taxicabs. The Idaho National Laboratory (INL), in conjunction with Ceramatec Inc. (Salt Lake City, USA) has been researching for several years the use of solid-oxide fuel cell technology to electrolyze steam for large-scale nuclear-powered hydrogen production. Now, an experimental research project is underway at the INL to investigate the feasibility of producing syngas by simultaneously electrolyzing at high-temperature steam and carbon dioxide (CO2) using solid oxide fuel cell technology. High-temperature nuclear reactors have the potential for substantially increasing the efficiency of syn-gas production from CO2 and water, with no consumption of fossil fuels, and no production of greenhouse gases. Thermal CO2-splitting and water splitting for syn-gas production can be accomplished via high-temperature electrolysis or thermochemical processes, using high-temperature nuclear process heat. In order to achieve competitive efficiencies, both processes require high-temperature operation (~850°C). High-temperature electrolytic CO2 and water splitting supported by nuclear process heat and electricity has the potential to produce syn-gas with an overall system efficiency near those of the thermochemical processes. Specifically, a high-temperature advanced nuclear reactor coupled with a high-efficiency high-temperature electrolyzer could achieve a competitive thermal-to-syn-gas conversion efficiency of 45 to

G. Hawkes; J. O' Brien; C. Stoots; S. Herring; R. Jones

2006-11-01T23:59:59.000Z

54

Basic Engineering Research for D and D of R Reactor Storage Pond Sludge: Electrokinetics, Carbon Dioxide Extraction, and Supercritical Water Oxidation  

Science Conference Proceedings (OSTI)

Large quantities of mixed low level waste (MLLW) that fall under the Toxic Substances Control Act (TSCA) exist and will continue to be generated during D and D operations at DOE sites across the country. The standard process for destruction of MLLW is incineration, which has an uncertain future. The extraction and destruction of PCBs from MLLW was the subject of this research Supercritical Fluid Extraction (SFE) with carbon dioxide with 5% ethanol as cosolvent and Supercritical Waster Oxidation (SCWO) were the processes studied in depth. The solid matrix for experimental extraction studies was Toxi-dry, a commonly used absorbent made from plant material. PCB surrogates were 1.2,4-trichlorobenzene (TCB) and 2-chlorobiphenyl (2CBP). Extraction pressures of 2,000 and 4,000 psi and temperatures of 40 and 80 C were studied. Higher extraction efficiencies were observed with cosolvent and at high temperature, but pressure little effect. SCWO treatment of the treatment of the PCB surrogates resulted in their destruction below detection limits.

Michael A. Matthews; David A. Bruce,; Thomas A. Davis; Mark C. Thies; John W. Weidner; Ralph E. White

2002-04-01T23:59:59.000Z

55

Ternary Electrocatalysts for Oxidizing Ethanol to Carbon Dioxide: Making Ir Capable of Splitting C-C bond  

Science Conference Proceedings (OSTI)

Splitting the C-C bond is the main obstacle to electroxidation of ethanol (EOR) to CO2. We recently demonstrated that the ternary PtRhSnO2 electrocatalyst can accomplish that reaction at room temperature with Rh having a unique capability to split the C-C bond. In this article we report the finding that Ir can be induced to split the C-C bond as a component of the ternary catalyst. We synthesized, characterized and compared the properties of several ternary electrocatalysts. Carbon-supported nanoparticle (NP) electrocatalysts comprising a SnO2 NP core decorated with multi-metallic nanoislands (MM = PtIr, PtRh, IrRh, PtIrRh) were prepared using a seeded growth approach. An array of characterization techniques were employed to establish the composition and architecture of the synthesized MM /SnO2 NPs, while electrochemical and in situ infrared reflection absorption spectroscopy studies elucidated trends in activity and the nature of the reaction intermediates and products. Both EOR reactivity and selectivity towards CO2 formation of several of these MM /SnO2/C electrocatalysts are significantly higher compared to conventional Pt/C and Pt/SnO2/C catalysts. We demonstrate that the PtIr/SnO2/C catalyst with high Ir content shows outstanding catalytic property with the most negative EOR onset potential and reasonably good selectivity towards ethanol complete oxidation to CO2. PtRh/SnO2/C catalysts with a moderate Rh content exhibit the highest EOR selectivity, as deduced from infrared studies.

Li, Meng [Brookhaven National Laboratory (BNL); Cullen, David A [ORNL; Sasaki, Kotaro [Brookhaven National Laboratory (BNL); Marinkovic, N. [University of Delaware; More, Karren Leslie [ORNL; Adzic, Radoslav R. [Brookhaven National Laboratory (BNL)

2013-01-01T23:59:59.000Z

56

Measurements of Surface Ocean Carbon Dioxide Partial Pressure During WOCE  

SciTech Connect

All of the technical goals of the World Ocean Circulation Experiment (WOCE) field program which were supported under the Department of Energy research grant ''Measurements of Surface Ocean Carbon Dioxide Partial Pressure During WOCE'' (DE-FG03-90ER60981) have been met. This has included the measurement of the partial pressures of carbon dioxide (C0{sub 2}) and nitrous oxide (N{sub 2}O) in both the surface ocean and the atmosphere on 24 separate shipboard expedition legs of the WOCE Hydrographic Programme. These measurements were made in the Pacific, Indian and Atlantic Oceans over a six-and-a-half year period, and over a distance of nearly 200,000 kilometers of ship track. The total number of measurements, including ocean measurements, air measurements and standard gas measurements, is about 136,000 for each gas, or about 34,000 measurements of each gas in the ocean and in the air. This global survey effort is directed at obtaining a better understanding of the role of the oceans in the global atmospheric budgets of two important natural and anthropogenic modulators of climate through the ''greenhouse effect'', CO{sub 2} and N{sub 2}O, and an important natural and anthropogenic modulator of the Earth's protective ozone layer through catalytic processes in the stratosphere, N{sub 2}O. For both of these compounds, the oceans play a major role in their global budgets. In the case of CO{sub 2}, roughly half of the anthropogenic production through the combustion of fossil fuels has been absorbed by the world's oceans. In the case of N{sub 2}O, roughly a third of the natural flux to the atmosphere originates in the oceans. As the interpretation of the variability in the oceanic distributions of these compounds improves, measurements such as those supported by this research project are playing an increasingly important role in improving our understanding of natural and anthropogenic influences on climate and ozone. (B204)

Weiss, R.F.

1998-10-15T23:59:59.000Z

57

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...

58

Global Warming and Greenhouse Gases  

Science Conference Proceedings (OSTI)

... NIST is producing new suites of primary gas standards for carbon dioxide, methane, carbon monoxide, and nitrous oxide in air at atmospheric levels ...

2013-09-20T23:59:59.000Z

59

NIST Kevin Douglass  

Science Conference Proceedings (OSTI)

... 1.6 micron atmospheric window region where three critical greenhouse gases, carbon dioxide (CO 2 ), nitrous oxide (N 2 O), and methane (CH 4 ...

2013-04-01T23:59:59.000Z

60

OIAF Products and Data Analyses Brochure, May 2000  

U.S. Energy Information Administration (EIA)

As required by the Energy Policy Act of 1992,this report presents the annual estimates of U.S.emissions for carbon dioxide, methane, nitrous oxide, ...

Note: This page contains sample records for the topic "dioxide nitrous oxide" 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

DISSOLUTION OF NEPTUNIUM OXIDE RESIDUES  

Science Conference Proceedings (OSTI)

This report describes the development of a dissolution flowsheet for neptunium (Np) oxide (NpO{sub 2}) residues (i.e., various NpO{sub 2} sources, HB-Line glovebox sweepings, and Savannah River National Laboratory (SRNL) thermogravimetric analysis samples). Samples of each type of materials proposed for processing were dissolved in a closed laboratory apparatus and the rate and total quantity of off-gas were measured. Samples of the off-gas were also analyzed. The quantity and type of solids remaining (when visible) were determined after post-dissolution filtration of the solution. Recommended conditions for dissolution of the NpO{sub 2} residues are: Solution Matrix and Loading: {approx}50 g Np/L (750 g Np in 15 L of dissolver solution), using 8 M nitric acid (HNO{sub 3}), 0.025 M potassium fluoride (KF) at greater than 100 C for at least 3 hours. Off-gas: Analysis of the off-gas indicated nitric oxide (NO), nitrogen dioxide (NO{sub 2}) and nitrous oxide (N{sub 2}O) as the only identified components. No hydrogen (H{sub 2}) was detected. The molar ratio of off-gas produced per mole of Np dissolved ranged from 0.25 to 0.4 moles of gas per mole of Np dissolved. A peak off-gas rate of {approx}0.1 scfm/kg bulk oxide was observed. Residual Solids: Pure NpO{sub 2} dissolved with little or no residue with the proposed flowsheet but the NpCo and both sweepings samples left visible solid residue after dissolution. For the NpCo and Part II Sweepings samples the residue amounted to {approx}1% of the initial material, but for the Part I Sweepings sample, the residue amounted to {approx}8 % of the initial material. These residues contained primarily aluminum (Al) and silicon (Si) compounds that did not completely dissolve under the flowsheet conditions. The residues from both sweepings samples contained minor amounts of plutonium (Pu) particles. Overall, the undissolved Np and Pu particles in the residues were a very small fraction of the total solids.

Kyser, E

2009-01-12T23:59:59.000Z

62

Carbon Dioxide Compression  

Science Conference Proceedings (OSTI)

Page 1. © C opyright 2009 Carbon Dioxide Compression DOE – EPRI – NIST ... Greenhouse gas sequestration Page 5. 5 © C opyright 2009 ...

2013-04-22T23:59:59.000Z

63

Formation of rare earth carbonates using supercritical carbon dioxide  

DOE Patents (OSTI)

The invention relates to a process for the rapid, high yield conversion of select rare earth oxides or hydroxides, to their corresponding carbonates by contact with supercritical carbon dioxide.

Fernando, Quintus (Tucson, AZ); Yanagihara, Naohisa (Zacopan, MX); Dyke, James T. (Santa Fe, NM); Vemulapalli, Krishna (Tuscon, AZ)

1991-09-03T23:59:59.000Z

64

Carbon dioxide capture process with regenerable sorbents  

DOE Patents (OSTI)

A process to remove carbon dioxide from a gas stream using a cross-flow, or a moving-bed reactor. In the reactor the gas contacts an active material that is an alkali-metal compound, such as an alkali-metal carbonate, alkali-metal oxide, or alkali-metal hydroxide; or in the alternative, an alkaline-earth metal compound, such as an alkaline-earth metal carbonate, alkaline-earth metal oxide, or alkaline-earth metal hydroxide. The active material can be used by itself or supported on a substrate of carbon, alumina, silica, titania or aluminosilicate. When the active material is an alkali-metal compound, the carbon-dioxide reacts with the metal compound to generate bicarbonate. When the active material is an alkaline-earth metal, the carbon dioxide reacts with the metal compound to generate carbonate. Spent sorbent containing the bicarbonate or carbonate is moved to a second reactor where it is heated or treated with a reducing agent such as, natural gas, methane, carbon monoxide hydrogen, or a synthesis gas comprising of a combination of carbon monoxide and hydrogen. The heat or reducing agent releases carbon dioxide gas and regenerates the active material for use as the sorbent material in the first reactor. New sorbent may be added to the regenerated sorbent prior to subsequent passes in the carbon dioxide removal reactor.

Pennline, Henry W. (Bethel Park, PA); Hoffman, James S. (Library, PA)

2002-05-14T23:59:59.000Z

65

The use of onboard diagnostics to reduce emissions in automobiles  

E-Print Network (OSTI)

The emissions from automobiles are very harmful and include gases such as Carbon Dioxide, Nitrous Oxide, and Sulfur Dioxide. One of the main reasons OBD was created was to control emissions however it currently only monitors ...

Perez, Alberto, Jr

2009-01-01T23:59:59.000Z

66

Ti3+ in the surface of titanium dioxide: generation, properties and photocatalytic application  

Science Conference Proceedings (OSTI)

Titanium dioxide (TiO2) is the most investigated crystalline oxide in the surface science of metal oxides. Its physical and chemical properties are dominantly determined by its surface condition. Ti3+ surface defect (TSD) is one ...

Liang-Bin Xiong; Jia-Lin Li; Bo Yang; Ying Yu

2012-01-01T23:59:59.000Z

67

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

68

sulfur dioxide emissions | OpenEI  

Open Energy Info (EERE)

sulfur dioxide emissions sulfur dioxide emissions Dataset Summary Description Emissions from energy use in buildings are usually estimated on an annual basis using annual average multipliers. Using annual numbers provides a reasonable estimation of emissions, but it provides no indication of the temporal nature of the emissions. Therefore, there is no way of understanding the impact on emissions from load shifting and peak shaving technologies such as thermal energy storage, on-site renewable energy, and demand control. Source NREL Date Released April 11th, 2011 (3 years ago) Date Updated April 11th, 2011 (3 years ago) Keywords buildings carbon dioxide emissions carbon footprinting CO2 commercial buildings electricity emission factors ERCOT hourly emission factors interconnect nitrogen oxides

69

CYCLIC CARBON DIOXIDE STIMULATION  

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

CARBON DIOXIDE STIMULATION ("Huff-and-Puff') (A well-stimulation method) Cyclic CO 2 stimulation is a single-well operation that is developing as a method of rapidly producing oil....

70

Sulfur Dioxide Regulations (Ohio)  

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

This chapter of the law establishes that the Ohio Environmental Protection Agency provides sulfur dioxide emission limits for every county, as well as regulations for the emission, monitoring and...

71

SRD 134 Carbon Dioxide  

Science Conference Proceedings (OSTI)

> Return to SRD 134, Index of Semiconductor Process Gases. CARBON DIOXIDE. MW [1]. 44.010. NBP [1]. 194.75 K. TP [1]. 216.59 K. CO 2. Pc [1]. ...

2012-07-27T23:59:59.000Z

72

Biomass Burning and the Production of Greenhouse Gases  

Science Conference Proceedings (OSTI)

Biomass burning is a source of greenhouse gases, carbon dioxide, methane, and nitrous oxide. In addition, biomass burning is a source of chemically active gases, including carbon monoxide, nonmethane hydrocarbons, and nitric oxide. These gases, along ...

Levine J. S.

1994-01-01T23:59:59.000Z

73

BEHAVIOR OF METALLIC INCLUSIONS IN URANIUM DIOXIDE  

E-Print Network (OSTI)

Metallic Inclusions in Uranium Dioxide", LBL-11117 (1980).in Hypostoichiornetric Uranium Dioxide 11 , LBL-11095 (OF METALLIC INCLUSIONS IN URANIUM DIOXIDE Rosa L. Yang and

Yang, Rosa L.

2013-01-01T23:59:59.000Z

74

SOOT-CATALYZED OXIDATION OF SULFUR DIOXIDE  

E-Print Network (OSTI)

produced by combustion of propane saturated with benzeneparticles produced by a propane flame. investigators foundand carbon(ls) regions of propane soot particles produced by

Chang, S.G.

2010-01-01T23:59:59.000Z

75

Voluntary Reporting of Greenhouse Gases Program - Electricity Factors  

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

Voluntary Reporting Program > Coefficients Voluntary Reporting Program > Coefficients Voluntary Reporting of Greenhouse Gases Program (Voluntary Reporting of Greenhouse Gases Program Fuel Carbon Dioxide Emission Coefficients) Voluntary Reporting of Greenhouse Gases Program Fuel Emission Coefficients Table 1: Carbon Dioxide Emission Factors for Stationary Combustion Table 2: Carbon Dioxide Emission Factors for Transportation Fuels Table 3: Generic Methane and Nitrous Oxide Emission Factors for Stationary Fuel Combustion Table 4: Specific Methane and Nitrous Oxide Emission Factors for Biogenic Fuel Sources Table 5: Methane and Nitrous Oxide Emissions Factors for Highway Vehicles Table 6: Methane and Nitrous Oxide Emission Factors for Alternative Fuel Vehicles Table 7: Methane and Nitrous Oxide Emission Factors for Non-Highway Mobile Combustion

76

METHOD OF SINTERING URANIUM DIOXIDE  

DOE Green Energy (OSTI)

This patent relates to a method of sintering uranium dioxide. Uranium dioxide bodies are heated to above 1200 nif- C in hydrogen, sintered in steam, and then cooled in hydrogen. (AEC)

Henderson, C.M.; Stavrolakis, J.A.

1963-04-30T23:59:59.000Z

77

Depleted Uranium (DU) Dioxide Fill  

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

Fill Depleted Uranium (DU) Dioxide Fill DU dioxide in the form of sand may be used to fill the void spaces in the waste package after the package is loaded with SNF. This...

78

Available Technologies: Acceleration of Carbon Dioxide ...  

APPLICATIONS OF TECHNOLOGY: Carbon dioxide capture and sequestration; ADVANTAGES: Accelerated capture of carbon dioxide; Effective at extremely dilute (nanomolar ...

79

APPENDIX F: EMISSIONS OF NITROUS OXIDE AND METHANE FROM ALTERNATIVE FUELS FOR MOTOR  

E-Print Network (OSTI)

for Improving Efficiency and Versatility of Dye-Sensitized Solar Cells ... PM 307 (Convention Center ) Pisist The operation and efficiency of dye-sensitized solar cells (DSSCs) ... Macromolecular Crowding Effects by Supported Wox/SiO2 Catalysts ... Center ) Israel E. Wachs1, Soe Lwin1, Wu Zhou2, Chris K. Kiely3, Nikolaos

Delucchi, Mark

80

800,000 Year Ice-Core Records of Atmospheric Nitrous Oxide (N2O...  

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

create a long-term record to the present. These records are maintained by the World Data Center for Paleoclimatology, National Oceanic and Atmospheric Administration (NOAA), and...

Note: This page contains sample records for the topic "dioxide nitrous oxide" 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

Table 11.4 Nitrous Oxide Emissions, 1980-2009 (Thousand Metric ...  

U.S. Energy Information Administration (EIA)

States 2009 (March 2011), Table 22; and EIA estimates based on the Intergovernmental Panel on Climate Change's Guidelines for National Greenhouse Gas Inventories ...

82

On-farm Assessment of Nitrogen Fertilizer application to corn on Nitrous Oxide Emissions  

E-Print Network (OSTI)

in soils cropped to corn with varying N fertilization. Can.as affected by tillage, corn-soybean-alfalfa rotations, andsoil nitrogen mineralization for corn production in eastern

2009-01-01T23:59:59.000Z

83

Table 11.4 Nitrous Oxide Emissions, 1980-2009 (Thousand Metric ...  

U.S. Energy Information Administration (EIA)

Short-Term Energy Outlook › Annual Energy Outlook › Energy Disruptions › International Energy Outlook ... 1984: 86: 45: 132: 1: 11: 11: 355: 2: 74: 431: 87: 661:

84

Quantification of and Controls on Dinitrogen and Nitrous Oxide Fluxes from Terrestrial Ecosystems  

E-Print Network (OSTI)

and then 100 g was weighed into each sample jar (490 mL).The jars were sealed on viton gaskets with aluminum lidssepta for gas sampling. The jars were flushed with N 2 for

Yang, Wendy Hui-I

2010-01-01T23:59:59.000Z

85

The carbon dioxide dilemma  

SciTech Connect

The effect of burning fossil fuels on the global climate is discussed. It may be that as we produce carbon dioxide by burning fossil fuels, we create a greenhouse effect which causes temperatures on earth to rise. Implications of changes in global temperatures are discussed.

Edelson, E.

1982-02-01T23:59:59.000Z

86

Carbon dioxide sensor  

SciTech Connect

The present invention generally relates to carbon dioxide (CO.sub.2) sensors. In one embodiment, the present invention relates to a carbon dioxide (CO.sub.2) sensor that incorporates lithium phosphate (Li.sub.3PO.sub.4) as an electrolyte and sensing electrode comprising a combination of lithium carbonate (Li.sub.2CO.sub.3) and barium carbonate (BaCO.sub.3). In another embodiment, the present invention relates to a carbon dioxide (CO.sub.2) sensor has a reduced sensitivity to humidity due to a sensing electrode with a layered structure of lithium carbonate and barium carbonate. In still another embodiment, the present invention relates to a method of producing carbon dioxide (CO.sub.2) sensors having lithium phosphate (Li.sub.3PO.sub.4) as an electrolyte and sensing electrode comprising a combination of lithium carbonate (Li.sub.2CO.sub.3) and barium carbonate (BaCO.sub.3).

Dutta, Prabir K. (Worthington, OH); Lee, Inhee (Columbus, OH); Akbar, Sheikh A. (Hilliard, OH)

2011-11-15T23:59:59.000Z

87

NETL: Carbon Dioxide 101 FAQs  

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

is carbon dioxide? is carbon dioxide? CO2 Dipole Carbon Dioxide Carbon dioxide (chemical name CO2) is a clear gas composed of one atom of carbon (C) and two atoms of oxygen (O). Carbon dioxide is one of many chemical forms of carbon on the Earth. It does not burn, and in standard temperature and pressure conditions it is stable, inert, and non-toxic. Carbon dioxide occurs naturally in small amounts (about 0.04%) in the Earth's atmosphere. The volume of CO2 in the atmosphere is equivalent to one individual in a crowd of 2,500. Carbon dioxide is produced naturally by processes deep within the Earth. This CO2 can be released at the surface by volcanoes or might be trapped in natural underground geologic CO2 deposits, similar to underground deposits of oil and natural gas. As a major greenhouse gas, CO2 helps create and

88

CARBON DIOXIDE FIXATION.  

DOE Green Energy (OSTI)

Solar carbon dioxide fixation offers the possibility of a renewable source of chemicals and fuels in the future. Its realization rests on future advances in the efficiency of solar energy collection and development of suitable catalysts for CO{sub 2} conversion. Recent achievements in the efficiency of solar energy conversion and in catalysis suggest that this approach holds a great deal of promise for contributing to future needs for fuels and chemicals.

FUJITA,E.

2000-01-12T23:59:59.000Z

89

Abatement of Air Pollution: Control of Carbon Dioxide Emissions...  

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

Carbon Dioxide EmissionsCarbon Dioxide Budget Trading Program (Connecticut) Abatement of Air Pollution: Control of Carbon Dioxide EmissionsCarbon Dioxide Budget Trading Program...

90

Radiation Effects in Oxide Ceramics and Novel LWR Fuels  

Science Conference Proceedings (OSTI)

Nuclear fuels, such as uranium dioxide (UO2) and Mixed Oxide (MOX) fuels, have been used in current light water reactors (LWRs) to produce about 15% of the ... of oxide ceramics for nuclear applications through experiment, theory and ...

91

NETL: Carbon Dioxide 101 FAQs  

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

the process through which carbon is cycled through the air, ground, plants, animals, and fossil fuels. People and animals inhale oxygen from the air and exhale carbon dioxide...

92

Sonochemical reduction of carbon dioxide.  

E-Print Network (OSTI)

??Emissions from the combustion of fossil fuels and cement production are responsible for approximately 75% of the increase of carbon dioxide (CO2) concentration in the… (more)

Koblov, Alexander

2011-01-01T23:59:59.000Z

93

State-level Greenhouse Gas Emission Factors for Electricity Generation, Updated 2002  

Reports and Publications (EIA)

This report documents the preparation of updated state-level electricity coefficients for carbon dioxide (CO ), methane (CH ), and nitrous oxide (N O), which represent a three-year weighted average for 1998-2000.

Information Center

2002-04-01T23:59:59.000Z

94

Power Technologies Energy Data Book: Fourth Edition, Chapter...  

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

Table 12.7 - Global Warming Potentials (GWP) (100-year time horizon) Gas GWP SAR 900 Carbon dioxide (CO2) 1 Methane (CH 4 ) 1 21 Nitrous oxide (N 2 O) 310 HFC-23 11,700 HFC-32 650...

95

Emissions of Greenhouse Gases in the United States, 2004  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

2005-12-19T23:59:59.000Z

96

Emissions of Greenhouse Gases in the United States, 2002  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

2003-10-01T23:59:59.000Z

97

Emissions of Greenhouse Gases in the United States, 2005  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

2006-11-14T23:59:59.000Z

98

Emissions of Greenhouse Gases in the United States, 1996  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

1997-10-01T23:59:59.000Z

99

Emissions of Greenhouse Gases in the United States, 1995  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

1996-10-01T23:59:59.000Z

100

Emissions of Greenhouse Gases in the United States, 1994  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

1995-09-01T23:59:59.000Z

Note: This page contains sample records for the topic "dioxide nitrous oxide" 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

Emissions of Greenhouse Gases in the United States, 1999  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

2000-10-01T23:59:59.000Z

102

Emissions of Greenhouse Gases in the United States, 2000  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

2001-11-01T23:59:59.000Z

103

Emissions of Greenhouse Gases in the United States, 1997  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

1998-10-01T23:59:59.000Z

104

Emissions of Greenhouse Gases in the United States, 1998  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

1999-10-01T23:59:59.000Z

105

Emissions of Greenhouse Gases in the United States, 2001  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

2002-12-01T23:59:59.000Z

106

Emissions of Greenhouse Gases in the United States, 2003  

Reports and Publications (EIA)

This report presents the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

2004-12-01T23:59:59.000Z

107

Emissions of Greenhouse Gases in the United States, 2000 Executive Summary  

Reports and Publications (EIA)

Executive Summary on the Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. These estimates are based on activity data and applied emissions factors and not on measured or metered emissions monitoring.

Perry Lindstrom

2001-11-01T23:59:59.000Z

108

Process for sequestering carbon dioxide and sulfur dioxide  

DOE Patents (OSTI)

A process for sequestering carbon dioxide, which includes reacting a silicate based material with an acid to form a suspension, and combining the suspension with carbon dioxide to create active carbonation of the silicate-based material, and thereafter producing a metal salt, silica and regenerating the acid in the liquid phase of the suspension.

Maroto-Valer, M. Mercedes (State College, PA); Zhang, Yinzhi (State College, PA); Kuchta, Matthew E. (State College, PA); Andresen, John M. (State College, PA); Fauth, Dan J. (Pittsburgh, PA)

2009-10-20T23:59:59.000Z

109

Method for hot pressing beryllium oxide articles  

DOE Patents (OSTI)

The hot pressing of beryllium oxide powder into high density compacts with little or no density gradients is achieved by employing a homogeneous blend of beryllium oxide powder with a lithium oxide sintering agent. The lithium oxide sintering agent is uniformly dispersed throughout the beryllium oxide powder by mixing lithium hydroxide in an aqueous solution with beryllium oxide powder. The lithium hydroxide is converted in situ to lithium carbonate by contacting or flooding the beryllium oxide - lithium hydroxide blend with a stream of carbon dioxide. The lithium carbonate is converted to lithium oxide while remaining fixed to the beryllium oxide particles during the hot pressing step to assure uniform density throughout the compact.

Ballard, A.H.; Godfrey, T.G. Jr.; Mowery, E.H.

1986-10-10T23:59:59.000Z

110

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

111

Optimize carbon dioxide sequestration, enhance oil recovery  

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

4 January Optimize carbon dioxide sequestration, enhance oil recovery Optimize carbon dioxide sequestration, enhance oil recovery The simulation provides an important...

112

Optimize carbon dioxide sequestration, enhance oil recovery  

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

Optimize carbon dioxide sequestration, enhance oil recovery Optimize carbon dioxide sequestration, enhance oil recovery The simulation provides an important approach to estimate...

113

Photocatalytic Conversion of Carbon Dioxide to Methanol.  

E-Print Network (OSTI)

??The photocatalytic conversion of carbon dioxide (CO2) to methanol was investigated. The procedure for the carbon dioxide conversion was carried out using a small scale… (more)

Okpo, Emmanuel

2009-01-01T23:59:59.000Z

114

Figure 37. Carbon dioxide emissions from electricity ...  

U.S. Energy Information Administration (EIA)

Sheet3 Sheet2 Sheet1 Figure 37. Carbon dioxide emissions from electricity generation in three cases, 2005-2040 (million metric tons carbon dioxide ...

115

China's Industrial Carbon Dioxide Emissions in Manufacturing...  

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

China's Industrial Carbon Dioxide Emissions in Manufacturing Subsectors and in Selected Provinces Title China's Industrial Carbon Dioxide Emissions in Manufacturing Subsectors and...

116

Thermochemical cyclic system for splitting water and/or carbon dioxide by means of cerium compounds and reactions useful therein  

DOE Patents (OSTI)

A thermochemical cyclic process for producing hydrogen from water comprises reacting ceric oxide with monobasic or dibasic alkali metal phosphate to yield a solid reaction product, oxygen and water. The solid reaction product, alkali metal carbonate or bicarbonate, and water, are reacted to yield hydrogen, ceric oxide, carbon dioxide and trialkali metal phosphate. Ceric oxide is recycled. Trialkali metal phosphate, carbon dioxide and water are reacted to yield monobasic or dibasic alkali metal phosphate and alkali metal bicarbonate, which are recycled. The cylic process can be modified for producing carbon monoxide from carbon dioxide by reacting the alkali metal cerous phosphate and alkali metal carbonate or bicarbonate in the absence of water to produce carbon monoxide, ceric oxide, carbon dioxide and trialkali metal phosphate. Carbon monoxide can be converted to hydrogen by the water gas shift reaction.

Bamberger, Carlos E. (Oak Ridge, TN); Robinson, Paul R. (Knoxville, TN)

1980-01-01T23:59:59.000Z

117

PREPARATION OF REFRACTORY OXIDE CRYSTALS  

DOE Patents (OSTI)

A method is given for preparing uranium dioxide, thorium oxide, and beryllium oxide in the form of enlarged individual crystals. The surface of a fused alkali metal halide melt containing dissolved uranium, thorium, or beryllium values is contacted with a water-vapor-bearing inert gas stream at a rate of 5 to 10 cubic centimeters per minute per square centimeter of melt surface area. Growth of individual crystals is obtained by prolonged contact. Beryllium oxide-coated uranium dioxide crystals are prepared by disposing uranium dioxide crystals 5 to 20 microns in diameter in a beryllium-containing melt and contacting the melt with a water-vapor-bearing inert gas stream in the same manner. (AEC)

Grimes, W.R.; Shaffer, J.H.; Watson, G.M.

1962-11-13T23:59:59.000Z

118

decommissioning of carbon dioxide (CO  

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

decommissioning of carbon dioxide (CO decommissioning of carbon dioxide (CO 2 ) storage wells. The manual builds on lessons learned through NETL research; the experiences of the Regional Carbon Sequestration Partnerships' (RCSPs) carbon capture, utilization, and storage (CCUS) field tests; and the acquired knowledge of industries that have been actively drilling wells for more than 100 years. In addition, the BPM provides an overview of the well-

119

METHOD OF MAKING PLUTONIUM DIOXIDE  

DOE Patents (OSTI)

A process is presented For converting both trivalent and tetravalent plutonium oxalate to substantially pure plutonium dioxide. The plutonium oxalate is carefully dried in the temperature range of 130 to300DEC by raising the temperature gnadually throughout this range. The temperature is then raised to 600 C in the period of about 0.3 of an hour and held at this level for about the same length of time to obtain the plutonium dioxide.

Garner, C.S.

1959-01-13T23:59:59.000Z

120

Calculating the probability of injected carbon dioxide plumes encountering faults  

E-Print Network (OSTI)

Change Special Report on Carbon Dioxide Capture and Storage,Probability of Injected Carbon Dioxide Plumes Encounteringthe probability of injected carbon dioxide encountering and

Jordan, P.D.

2013-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "dioxide nitrous oxide" 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

The Greenness of Cities: Carbon Dioxide Emissions and Urban Development  

E-Print Network (OSTI)

carbon dioxide emissions index, we use conversion factors.conversion factor of pounds of carbon dioxide emitted perappropriate factors to arrive at carbon dioxide emissions.

Glaeser, Edward L.; Kahn, Matthew E.

2008-01-01T23:59:59.000Z

122

The Greenness of Cities: Carbon Dioxide Emissions and Urban Development  

E-Print Network (OSTI)

carbon dioxide emissions index, we use conversion factors.into carbon dioxide emissions, we continue to use a factorappropriate factors to arrive at carbon dioxide emissions.

Glaeser, Edward L.; Kahn, Matthew E.

2008-01-01T23:59:59.000Z

123

Reaction products of chlorine dioxide  

E-Print Network (OSTI)

Concern over the presence of trihalomethanes and other chlorinated by-products in chlorinedisinfected drinking water has led to extensive investigations of treatment options for controlling these by-products. Among these treatment options is the use of an alternative disinfectant such as chlorine dioxide. Although chlorine dioxide does not react to produce trihalomethanes, considerable evidence does exist that chlorine dioxide, like chlorine, will produce other organic by-products. The literature describes chlorinated and nonchlorinated derivatives including acids, epoxides, quinones, aldehydes, disulfides, and sulfonic acids that are products of reactions carried out under conditions that are vastly different from those experienced during drinking water treatment. Evidence is beginning to emerge, however, that some by-products in these categories may be produced. Certain specific volatile aldehydes and halogenated derivatives as determined by the total organic halogen parameter are among those by-products that have been measured.

Alan A. Stevens

1982-01-01T23:59:59.000Z

124

Weyburn Carbon Dioxide Sequestration Project  

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

Weyburn Carbon DioxiDe SequeStration Weyburn Carbon DioxiDe SequeStration ProjeCt Background Since September 2000, carbon dioxide (CO 2 ) has been transported from the Dakota Gasification Plant in North Dakota through a 320-km pipeline and injected into the Weyburn oilfield in Saskatchewan, Canada. The CO 2 has given the Weyburn field, discovered 50 years ago, a new life: 155 million gross barrels of incremental oil are slated to be recovered by 2035 and the field is projected to be able to store 30 million tonnes of CO 2 over 30 years. CO 2 injection began in October of 2005 at the adjacent Midale oilfield, and an additional 45-60 million barrels of oil are expected to be recovered during 30 years of continued operation. A significant monitoring project associated with the Weyburn and Midale commercial

125

Destruction of organic wastes with molten oxidizers  

DOE Patents (OSTI)

A process for destruction of biologically hazardous organic chemical wastes by using liquefied strongly oxidizing inorganic salts, such as the alkali metal nitrates, at high temperatures and atmospheric pressure, to yield inorganic salts, carbon dioxide, and water. The oxidizing salts are regenerated and recycled.

Bradshaw, R.W.; Holmes, J.T.; Tyner, C.E.

1990-01-01T23:59:59.000Z

126

Destruction of organic wastes with molten oxidizers  

DOE Patents (OSTI)

A process for destruction of biologically hazardous organic chemical wastes by using liquefied strongly oxidizing inorganic salts, such as the alkali metal nitrates, at high temperatures and atmospheric pressure, to yield inorganic salts, carbon dioxide, and water. The oxidizing salts are regenerated and recycled.

Bradshaw, R.W.; Holmes, J.T.; Tyner, C.E.

1990-12-31T23:59:59.000Z

127

Plasma gasification of coal in different oxidants  

Science Conference Proceedings (OSTI)

Oxidant selection is the highest priority for advanced coal gasification-process development. This paper presents comparative analysis of the Powder River Basin bituminous-coal gasification processes for entrained-flow plasma gasifier. Several oxidants, which might be employed for perspective commercial applications, have been chosen, including air, steam/carbon-dioxide blend, carbon dioxide, steam, steam/air, steam/oxygen, and oxygen. Synthesis gas composition, carbon gasification degree, specific power consumptions, and power efficiency for these processes were determined. The influence of the selected oxidant composition on the gasification-process main characteristics have been investigated.

Matveev, I.B.; Messerle, V.E.; Ustimenko, A.B. [Applied Plasma Technology, Mclean, VA (USA)

2008-12-15T23:59:59.000Z

128

SEPARATING PROTOACTINIUM WITH MANGANESE DIOXIDE  

DOE Patents (OSTI)

The preparation of U/sup 235/ and an improved method for isolating Pa/ sup 233/ from foreign products present in neutronirradiated thorium is described. The method comprises forming a solution of neutron-irradiated thorium together with a manganous salt, then adding potassium permanganate to precipitate the manganese as manganese dioxide whereby protoactinium is carried down with the nnanganese dioxide dissolving the precipitate, adding a soluble zirconium salt, and adding phosphate ion to precipitate zirconium phosphate whereby protoactinium is then carried down with the zirconium phosphate to effect a further concentration.

Seaborg, G.T.; Gofman, J.W.; Stoughton, R.W.

1958-04-22T23:59:59.000Z

129

Erbium diffusion in silicon dioxide  

SciTech Connect

Erbium diffusion in silicon dioxide layers prepared by magnetron sputtering, chemical vapor deposition, and thermal growth has been investigated by secondary ion mass spectrometry, and diffusion coefficients have been extracted from simulations based on Fick's second law of diffusion. Erbium diffusion in magnetron sputtered silicon dioxide from buried erbium distributions has in particular been studied, and in this case a simple Arrhenius law can describe the diffusivity with an activation energy of 5.3{+-}0.1 eV. Within a factor of two, the erbium diffusion coefficients at a given temperature are identical for all investigated matrices.

Lu Yingwei; Julsgaard, B.; Petersen, M. Christian [Department of Physics and Astronomy, Aarhus University, DK-8000 Aarhus C (Denmark); Jensen, R. V. Skougaard [Department of Physics and Nanotechnology, Aalborg University, DK-9220 Aalborg O (Denmark); Pedersen, T. Garm; Pedersen, K. [Department of Physics and Nanotechnology, Aalborg University, DK-9220 Aalborg O (Denmark); Interdisciplinary Nanoscience Center-iNANO, DK-8000 Aarhus C (Denmark); Larsen, A. Nylandsted [Department of Physics and Astronomy, Aarhus University, DK-8000 Aarhus C (Denmark); Interdisciplinary Nanoscience Center-iNANO, DK-8000 Aarhus C (Denmark)

2010-10-04T23:59:59.000Z

130

OXYGEN DIFFUSION IN HYPOSTOICHIOMETRIC URANIUM DIOXIDE  

E-Print Network (OSTI)

IN HYPOSTOICHIOMETRIC URANIUM DIOXIDE Kee Chul Kim Ph.D.727-366; Figure 1. Oxygen-uranium phase-equilibrium _ystem [18]. uranium dioxide powders and 18 0 enriched carbon

Kim, Kee Chul

2010-01-01T23:59:59.000Z

131

Carbon Dioxide Information Analysis Center (CDIAC)  

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

Emissions Carbon Dioxide Fossil-Fuel CO2 Emissions Carbon Dioxide Emissions from Fossil-Fuel Consumption and Cement Manufacture, (2011) Kyoto-Related Fossil-Fuel CO2 Emission...

132

Flame Inhibition by Ferrocene, Carbon Dioxide, and ...  

Science Conference Proceedings (OSTI)

Flame Inhibition by Ferrocene, Carbon Dioxide, and Trifluoromethane Blends: Synergistic ... a straight sided schlieren image which is captured by a ...

2012-10-23T23:59:59.000Z

133

Application Of Optical Processing For Growth Of Silicon Dioxide  

DOE Patents (OSTI)

A process for producing a silicon dioxide film on a surface of a silicon substrate. The process comprises illuminating a silicon substrate in a substantially pure oxygen atmosphere with a broad spectrum of visible and infrared light at an optical power density of from about 3 watts/cm.sup.2 to about 6 watts/cm.sup.2 for a time period sufficient to produce a silicon dioxide film on the surface of the silicon substrate. An optimum optical power density is about 4 watts/cm.sup.2 for growth of a 100.ANG.-300.ANG. film at a resultant temperature of about 400.degree. C. Deep level transient spectroscopy analysis detects no measurable impurities introduced into the silicon substrate during silicon oxide production and shows the interface state density at the SiO.sub.2 /Si interface to be very low.

Sopori, Bhushan L. (Denver, CO)

1997-06-17T23:59:59.000Z

134

Carbon dioxide for enhanced oil recovery  

SciTech Connect

The current status and outlook for carbon dioxide in the immediate future has been examined by Kenneth M. Stern of Chem Systems Inc. Stern. Most of the tonnage carbon dioxide being used for EOR comes from natural gas wells. Major projects are now in progress to develop natural carbon dioxide sources and to transport the gas via pipeline to the injection region. These projects and the maximum permissible cost of carbon dioxide at current petroleum prices are discussed. Potential sources include exhaust gases from power plants, natural gas processing plants, chemical plants, and natural carbon dioxide wells.

Not Available

1986-04-28T23:59:59.000Z

135

Nitrous Oxide and Molecular Nitrogen Isotopic Compositions and Aerosol Optical Properties: Experiments and Observations Relevant to Planetary Atmospheres  

E-Print Network (OSTI)

D6), doi:10.1029/1096JD03382. Volk, C. M. , et al. (1996),CIRS, Icarus , 191 , 712-721. Volk, C. M. , et al. (1996),Mass Spectrom. , 22, 603-312. Volk, C. M. , et al. (1996),

Croteau, Philip Louis

2010-01-01T23:59:59.000Z

136

Nitrous oxide as a substitute for sulfur hexafluoride in the ANSI/ASHRAE 110 Method of hood performance evaluation.  

E-Print Network (OSTI)

??The ANSI/ASHRAE 110 Method is the standard test for laboratory hood containment performance. Sulfur hexafluoride is specified as the gas most suitable for this test… (more)

Guffey, Eric J. (Eric Jemison)

2011-01-01T23:59:59.000Z

137

Nitrous oxide as a substitute for sulfur hexafluoride in the ANSI/ASHRAE 110 Method of hood performance evaluation  

E-Print Network (OSTI)

The ANSI/ASHRAE 110 Method is the standard test for laboratory hood containment performance. Sulfur hexafluoride is specified as the gas most suitable for this test and is most commonly used. Sulfur hexafluoride use has ...

Guffey, Eric J. (Eric Jemison)

2011-01-01T23:59:59.000Z

138

Nitrous Oxide and Molecular Nitrogen Isotopic Compositions and Aerosol Optical Properties: Experiments and Observations Relevant to Planetary Atmospheres  

E-Print Network (OSTI)

not included here). The solar spectrum at 625 km in Earth’ssee if structure in the solar spectrum changes the ratio ofnot included here). The solar spectrum at 625 km in Earth’s

Croteau, Philip Louis

2010-01-01T23:59:59.000Z

139

Nitrous Oxide and Molecular Nitrogen Isotopic Compositions and Aerosol Optical Properties: Experiments and Observations Relevant to Planetary Atmospheres  

E-Print Network (OSTI)

through biomass and fossil fuel combustion, which show thatof industrial combustion or biomass burning processes butbiomass burning, based on recent measurements of a combustion

Croteau, Philip Louis

2010-01-01T23:59:59.000Z

140

Capturing Carbon Dioxide From Air  

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

Capturing Carbon Dioxide From Air Capturing Carbon Dioxide From Air Klaus S. Lackner (kl2010@columbia.edu; 212-854-0304) Columbia University 500 West 120th Street New York, NY 10027 Patrick Grimes (pgrimes@worldnet.att.net; 908-232-1134) Grimes Associates Scotch Plains, NJ 07076 Hans-J. Ziock (ziock@lanl.gov; 505-667-7265) Los Alamos National Laboratory P.O.Box 1663 Los Alamos, NM 87544 Abstract The goal of carbon sequestration is to take CO 2 that would otherwise accumulate in the atmosphere and put it in safe and permanent storage. Most proposed methods would capture CO 2 from concentrated sources like power plants. Indeed, on-site capture is the most sensible approach for large sources and initially offers the most cost-effective avenue to sequestration. For distributed, mobile sources like cars, on-board capture at affordable cost would not be

Note: This page contains sample records for the topic "dioxide nitrous oxide" 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

Reductive Sequestration of Carbon Dioxide  

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

Reductive Sequestration of Carbon Dioxide Reductive Sequestration of Carbon Dioxide T. Mill (ted.mill@sri.com; 650-859-3605) SRI, PS273 333 Ravenswood Menlo Park, CA 94025 D. Ross (dsross3@yahoo.com; 650-327-3842) U.S. Geological Survey, Bldg 15 MS 999 345 Middlefield Rd. Menlo Park, CA 94025 Introduction The United States currently meets 80% of its energy needs by burning fossil fuels to form CO 2 . The combustion-based production of CO 2 has evolved into a major environmental challenge that extends beyond national borders and the issue has become as politically charged as it is technologically demanding. Whereas CO 2 levels in the atmosphere had remained stable over the 10,000 years preceeding the industrial revolution, that event initiated rapid growth in CO 2 levels over the past 150 years (Stevens, 2000). The resulting accelerating accumulation of

142

IEP - Carbon Dioxide: Regulatory Drivers  

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

IEP - Carbon Dioxide (CO2) Regulatory Drivers In July 7, 2009 testimony before the U.S. Senate Committee on Environment and Public Works, Secretary of Energy Steven Chu made the following statements:1 "...Overwhelming scientific evidence shows that carbon dioxide from human activity has increased the atmospheric level of CO2 by roughly 40 percent, a level one- third higher than any time in the last 800,000 years. There is also a consensus that CO2 and other greenhouse gas emissions have caused our planet to change. Already, we have seen the loss of about half of the summer arctic polar ice cap since the 1950s, a dramatically accelerating rise in sea level, and the loss of over two thousand cubic miles of glacial ice, not on geological time scales but over a mere hundred years.

143

Carbon Dioxide Compression and Transportation  

Science Conference Proceedings (OSTI)

This report summarizes the state of the art regarding carbon dioxide CO2 compression and transportation in the United States and Canada. The primary focus of the report was on CO2 compression because it is a significant cost and energy penalty in carbon capture and storage CCS. The secondary focus of the report was to document the state of the art of CO2 pipeline transportation in the United States and Canada.

2008-12-23T23:59:59.000Z

144

Method for Sequestering Carbon Dioxide and Sulfur Dioxide Utilizing a Plurality of Waste Streams  

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

Sequestering Carbon Dioxide and Sulfur Dioxide Sequestering Carbon Dioxide and Sulfur Dioxide Utilizing a Plurality of Waste Streams Opportunity The Department of Energy's National Energy Technology Laboratory is seeking licensing partners interested in implementing United States Patent Number 7,922,792 entitled "Method for Sequestering Carbon Dioxide and Sulfur Dioxide Utilizing a Plurality of Waste Streams." Disclosed in this patent is the invention of a neutralization/sequestration method that concomitantly treats bauxite residues from aluminum production processes, as well as brine wastewater from oil and gas production processes. The method uses an integrated approach that coincidentally treats multiple industrial waste by-product streams. The end results include neutralizing caustic

145

Carbon Dioxide: Threat or Opportunity?  

E-Print Network (OSTI)

Over the past century, fossil fuel consumption has added carbon dioxide to the atmosphere at rapidly increasing rates. The prospect of further acceleration of this rate by turning from petroleum to coal has alarmed climatologists because of possible catastrophic long term effects on world climate. An alternative to discharging carbon dioxide into the atmosphere is to find new uses. One possible use is in 'Biofactories'. Biofactories may be achieved by exploiting two new developing technologies: Solar (Photosynthesis) energy, and genetic engineering. Some exciting new developments in genetic engineering will be touched on together with established bio-engineering-aquaculture, hydroponics, yeast, pharmaceutical production, fermentation, single cell protein, etc. A 'bio-factory' will be described, with a feed stream of carbon dioxide, water, nutrients containing sulfur, nitrogen, phosphorus and trace elements, and living culture interacting with light under controlled conditions to yield food and raw materials. Candidate products will be suggested and a few of the problems anticipated. Engineering and logistic requirements will be outlined and the economic impact assessed.

McKinney, A. R.

1982-01-01T23:59:59.000Z

146

An experimental investigation of the urea-water decomposition and selective catalytic reduction (SCR) of nitric oxides with urea using V2O5-WO3-TiO2 catalyst.  

E-Print Network (OSTI)

Two flow reactor studies, using an electrically heated laminar flow reactor over Vanadia based (V2O5-WO3/TiO2) honeycomb catalyst, were performed at 1 atm pressure and various temperatures. The experiments were conducted using simulated exhaust gas compositions for different exhaust gases. A quartz tube was used in order to establish inert conditions inside the reactor. The experiments utilized a Fourier transform infrared (FTIR) spectrometer in order to perform both qualitative and quantitative analysis of the reaction products. Urea-water solution decomposition was investigated over V2O5-WO3/TiO2 catalyst over the entire SCR temperature range using the temperature controlled flow reactor. The solution was preheated and then injected into pure nitrogen (N2) stream. The decomposition experiments were conducted with a number of oxygen (O2) compositions (0, 1, 10, and 15%) over the temperature range of 227oC to 477oC. The study showed ammonia (NH3), carbon-dioxide (CO2) and nitric oxide (NO) as the major products of decomposition along with other products such as nitrous oxide (N2O) and nitrogen dioxide (NO2). The selective catalytic reduction (SCR) of nitric oxide (NO) with urea-water solution over V2O5-WO3/TiO2 catalyst using a laboratory laminar-flow reactor was investigated. Urea-water solution was injected at a temperature higher than the vaporization temperature of water and the flow reactor temperature was varied from 127oC to 477oC. A FTIR spectrometer was used to determine the concentrations of the product species. The major products of SCR reduction were NH3, NO and CO2 along with the presence of other minor products NO2 and N2O. NO removal of up to 87% was observed. The aim of the urea-water decomposition experiments was to study the decomposition process as close to the SCR configuration as possible. The aim of the SCR experiments was to delineate the effect of various parameters including reaction temperature and O2 concentration on the reduction process. The SCR investigation showed that changing parameter values significantly affected the NO removal, the residual NH3 concentration, the temperature of the maximum NO reduction, and the temperature of complete NH3 conversion. In the presence of O2, the reaction temperature for maximum NO reduction was 377?C for ratio of 1.0.

Johar, Jasmeet Singh

2005-08-01T23:59:59.000Z

147

PROCESS OF PRODUCING REFRACTORY URANIUM OXIDE ARTICLES  

DOE Patents (OSTI)

A method is presented for fabricating uranium oxide into a shaped refractory article by introducing a uranium halide fluxing reagent into the uranium oxide, and then mixing and compressing the materials into a shaped composite mass. The shaped mass of uranium oxide and uranium halide is then fired at an elevated temperature so as to form a refractory sintered article. It was found in the present invention that the introduction of a uraninm halide fluxing agent afforded a fluxing action with the uranium oxide particles and that excellent cohesion between these oxide particles was obtained. Approximately 90% of uranium dioxide and 10% of uranium tetrafluoride represent a preferred composition.

Hamilton, N.E.

1957-12-01T23:59:59.000Z

148

Methanol partial oxidation reformer  

DOE Patents (OSTI)

A partial oxidation reformer is described comprising a longitudinally extending chamber having a methanol, water and an air inlet and an outlet. An igniter mechanism is near the inlets for igniting a mixture of methanol and air, while a partial oxidation catalyst in the chamber is spaced from the inlets and converts methanol and oxygen to carbon dioxide and hydrogen. Controlling the oxygen to methanol mole ratio provides continuous slightly exothermic partial oxidation reactions of methanol and air producing hydrogen gas. The liquid is preferably injected in droplets having diameters less than 100 micrometers. The reformer is useful in a propulsion system for a vehicle which supplies a hydrogen-containing gas to the negative electrode of a fuel cell. 7 figs.

Ahmed, S.; Kumar, R.; Krumpelt, M.

1999-08-24T23:59:59.000Z

149

Methanol partial oxidation reformer  

DOE Patents (OSTI)

A partial oxidation reformer is described comprising a longitudinally extending chamber having a methanol, water and an air inlet and an outlet. An igniter mechanism is near the inlets for igniting a mixture of methanol and air, while a partial oxidation catalyst in the chamber is spaced from the inlets and converts methanol and oxygen to carbon dioxide and hydrogen. Controlling the oxygen to methanol mole ratio provides continuous slightly exothermic partial oxidation reactions of methanol and air producing hydrogen gas. The liquid is preferably injected in droplets having diameters less than 100 micrometers. The reformer is useful in a propulsion system for a vehicle which supplies a hydrogen-containing gas to the negative electrode of a fuel cell. 7 figs.

Ahmed, S.; Kumar, R.; Krumpelt, M.

1999-08-17T23:59:59.000Z

150

Method for hot pressing beryllium oxide articles  

DOE Patents (OSTI)

The hot pressing of beryllium oxide powder into high density compacts with little or no density gradients is achieved by employing a homogeneous blend of beryllium oxide powder with a lithium oxide sintering agent. The lithium oxide sintering agent is uniformly dispersed throughout the beryllium oxide powder by mixing lithium hydroxide in an aqueous solution with beryllium oxide powder. The lithium hydroxide is converted in situ to lithium carbonate by contacting or flooding the beryllium oxide-lithium hydroxide blend with a stream of carbon dioxide. The lithium carbonate is converted to lithium oxide while remaining fixed to the beryllium oxide particles during the hot pressing step to assure uniform density throughout the compact.

Ballard, Ambrose H. (Oak Ridge, TN); Godfrey, Jr., Thomas G. (Oak Ridge, TN); Mowery, Erb H. (Clinton, TN)

1988-01-01T23:59:59.000Z

151

Carbon dioxide and climate: a bibliography  

SciTech Connect

This bibliography with abstracts presents 394 citations retrieved from the Energy Data Base of the Department of Energy Technical Information Center, Oak Ridge, Tennessee. The citations cover all aspects of the climatic effects of carbon dioxide emissions to the atmosphere. These include carbon cycling, temperature effects, carbon dioxide control technologies, paleoclimatology, carbon dioxide sources and sinks, mathematical models, energy policies, greenhouse effect, and the role of the oceans and terrestrial forests.

Ringe, A.C. (ed.)

1980-10-01T23:59:59.000Z

152

TABLE OF CONTENTS Carbon Dioxide Reduction Metallurgy  

Science Conference Proceedings (OSTI)

Chemical Utilization of Sequestered Carbon Dioxide as a. Booster of Hydrogen ... CO2 Capture and Sequestration – Implications for the Metals. Industry.

153

Atmospheric carbon dioxide and the greenhouse effect  

SciTech Connect

This document contains a non-technical review of the problems associated with atmospheric carbon dioxide and the resulting greenhouse effect. (TEM)

Firestine, M.W. (ed.)

1989-05-01T23:59:59.000Z

154

Carbon Dioxide Transportation and Sequestration Act (Illinois...  

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

process for the issuance of a certificate of authority by an owner or operator of a pipeline designed, constructed, and operated to transport and to sequester carbon dioxide...

155

Carbon Ion Pump for Carbon Dioxide Removal  

coal fired power plants; oil or gas fired power plants; cement production; bio-fuel combustion; Separation of carbon dioxide from other combustion ...

156

Scientists Crack Materials Mystery of Vanadium Dioxide  

Science Conference Proceedings (OSTI)

Dec 1, 2010 ... Using a condensed physics theory to explain the observed phase behaviors of vanadium dioxide, ORNL scientists have discovered that the ...

157

EIA - Greenhouse Gas Emissions - Carbon Dioxide Emissions  

U.S. Energy Information Administration (EIA)

Nonfuel uses of fossil fuels (for purposes other than their energy value) create carbon dioxide emissions and also sequester carbon in nonfuel products, ...

158

Carbon Dioxide Information Analysis Center (CDIAC)  

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

available free of charge - include estimates of carbon dioxide emissions from fossil-fuel consumption and land-use changes; records of atmospheric concentrations of carbon...

159

Selective catalytic reduction (SCR) of nitric oxide (NO) with ammonia over vanadia-based and pillared interlayer clay-based catalysts  

E-Print Network (OSTI)

The selective catalytic reduction (SCR) of nitric oxide (NO) with ammonia over vanadia-based (V2O5-WO3/TiO2) and pillared interlayer clay-based (V2O5/Ti-PILC) monolithic honeycomb catalysts using a laboratory laminar-flow reactor was investigated. The experiments used a number of gas compositions to simulate different combustion gases. A Fourier transform infrared (FTIR) spectrometer was used to determine the concentrations of the product species. The major products were nitric oxide (NO), ammonia (NH3), nitrous oxide (N2O), and nitrogen dioxide (NO2). The aim was to delineate the effect of various parameters including reaction temperature, oxygen concentration, NH3-to-NO ratio, space velocity, heating area, catalyst arrangement, and vanadium coating on the removal of nitric oxide. The investigation showed that the change of the parameters significantly affected the removals of NO and NH3 species, the residual NH3 concentration (or NH3 slip), the temperature of the maximum NO reduction, and the temperature of complete NH3 conversion. The reaction temperature was increased from the ambient temperature (25°C) to 450 °C. For both catalysts, high NO and NH3 removals were obtained in the presence of a small amount of oxygen, but no significant influence was observed from 0.1 to 3.0% O2. An increase in NH3-to-NO ratio increased NO reduction but decreased NH3 conversions. For V2O5-WO3/TiO2, the decrease of space velocity increased NO and NH3 removals and broadened the active temperature window (based on NO > 88% and NH3 > 87%) about 50°C. An increase in heating area decreased the reaction temperature of the maximum NO reduction from 350 to 300°C, and caused the active reaction temperature window (between 250 and 400°C) to shift toward 50°C lower reaction temperatures (between 200 and 350°C). The change of catalyst arrangements resulted slight improvement for NO and NH3 removals, therefore, the change might contribute to more gas removals. The catalyst with extra vanadium coating showed higher NO reductions and NH3 conversions than the catalyst without the extra vanadium coating.

Oh, Hyuk Jin

2006-05-01T23:59:59.000Z

160

Power plant emissions of sulfur dioxide and nitrogen oxides ...  

U.S. Energy Information Administration (EIA)

Have a question, comment, or suggestion for a future article? Send your feedback to todayinenergy@eia.gov

Note: This page contains sample records for the topic "dioxide nitrous oxide" 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

Power plant emissions of sulfur dioxide and nitrogen oxides ...  

U.S. Energy Information Administration (EIA)

Nuclear & Uranium. Uranium fuel ... acid rain program in the eastern half of the United States. ... and settlements under the Clean Air Act's New Source Review ...

162

Power plant emissions of sulfur dioxide and nitrogen oxides ...  

U.S. Energy Information Administration (EIA)

State Energy Data System ... the program provided an economic incentive for coal-fired power plants to reduce emissions by installing pollution contro ...

163

Carbon dioxide storage professor Martin Blunt  

E-Print Network (OSTI)

Carbon dioxide storage professor Martin Blunt executive summary Carbon Capture and Storage (CCS) referS to the Set of technologies developed to capture carbon dioxide (Co2) gas from the exhausts raises new issues of liability and risk. the focus of this briefing paper is on the storage of carbon

164

ORNL DAAC, Effects of Increased Carbon Dioxide, Dec. 11, 2002  

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

Increased Carbon Dioxide on Vegetation The ORNL DAAC announces the release of a data set entitled "Effects of Elevated Carbon Dioxide on Litter Chemistry and Decomposition." The...

165

Geologic Carbon Dioxide Storage Field Projects Supported by DOE...  

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

Geologic Carbon Dioxide Storage Field Projects Supported by DOE's Sequestration Program Geologic Carbon Dioxide Storage Field Projects Supported by DOE's Sequestration Program...

166

Cost and Performance of Carbon Dioxide Capture from Power Generation...  

Open Energy Info (EERE)

on Facebook icon Twitter icon Cost and Performance of Carbon Dioxide Capture from Power Generation Jump to: navigation, search Name Cost and Performance of Carbon Dioxide...

167

Changes related to "Cost and Performance of Carbon Dioxide Capture...  

Open Energy Info (EERE)

icon Changes related to "Cost and Performance of Carbon Dioxide Capture from Power Generation" Cost and Performance of Carbon Dioxide Capture from Power Generation...

168

Why do carbon dioxide emissions weigh more than the ...  

U.S. Energy Information Administration (EIA)

Why do carbon dioxide emissions weigh more than the original fuel? Carbon dioxide emissions weigh more than the original fuel because during complete ...

169

Recovery Act: Re-utilization of Industrial Carbon Dioxide for...  

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

Re-utilization of Industrial Carbon Dioxide for Algae Production Using a Phase Change Material Background Worldwide carbon dioxide (CO 2 ) emissions from human activity have...

170

EA-1336: Ocean Sequestration of Carbon Dioxide Field Experiment...  

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

6: Ocean Sequestration of Carbon Dioxide Field Experiment, Pittsburgh, Pennsylvania EA-1336: Ocean Sequestration of Carbon Dioxide Field Experiment, Pittsburgh, Pennsylvania...

171

Haverford Researchers Create Carbon Dioxide-Separating Polymer  

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

Haverford College Researchers Create Carbon Dioxide-Separating Polymer Haverford College Researchers Create Carbon Dioxide-Separating Polymer August 1, 2012 | Tags: Basic Energy...

172

Improving the Carbon Dioxide Emission Estimates from the Combustion...  

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

Improving the Carbon Dioxide Emission Estimates from the Combustion of Fossil Fuels in California and Spatial Disaggregated Estimate of Energy-related Carbon Dioxide for California...

173

Improving the Carbon Dioxide Emission Estimates from the Combustion...  

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

the Carbon Dioxide Emission Estimates from the Combustion of Fossil Fuels in California Title Improving the Carbon Dioxide Emission Estimates from the Combustion of Fossil Fuels in...

174

Emerging Energy-efficiency and Carbon Dioxide Emissions-reduction...  

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

Energy-efficiency and Carbon Dioxide Emissions-reduction Technologies for the Iron and Steel Industry Title Emerging Energy-efficiency and Carbon Dioxide Emissions-reduction...

175

Carbon Dioxide Capture/Sequestration Tax Deduction (Kansas) ...  

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

Carbon Dioxide CaptureSequestration Tax Deduction (Kansas) Carbon Dioxide CaptureSequestration Tax Deduction (Kansas) Eligibility Commercial Industrial Utility Program...

176

Nano-Enabled Titanium Dioxide Ultraviolet Protective Layers for...  

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

Nano-Enabled Titanium Dioxide Ultraviolet Protective Layers for Cool-Color Roofing Research Project Nano-Enabled Titanium Dioxide Ultraviolet Protective Layers for Cool-Color...

177

Molten salt synthesis and localized surface plasmon resonance study of vanadium dioxide nanopowders  

SciTech Connect

Rutile-type vanadium dioxide nanopowders with four different sizes were successfully synthesized by carbothermal reducing V{sub 2}O{sub 5} in KCl-LiCl molten salt. XRD and TEM characterizations suggested that vanadium dioxide particles formed by a broken and reunited process of vanadium oxide. Molten salt and organic carbon sources are crucial to the size of final particles. In the presence of the molten salt, the organic carbon with a shorter chain length would induce smaller particles. The UV-VIS-IR spectral measurements for as-prepared vanadium dioxide announced an obvious localized surface plasmon resonance band in the near infrared region at 90 deg. C. - Graphical abstract: Schematic illustration of the formation mechanism of VO{sub 2}(M) nanoparticles in molten salt, particles size can be controlled by choosing organic carbon sources with different chain length.

Wang Fu [Key Laboratory of Photochemical Conversion and Optoelectronic Materials of Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Zhongguancun, Beijing 100190 (China); Graduate School of the Chinese Academy of Sciences, Beijing 100806 (China); Liu Yun [Key Laboratory of Photochemical Conversion and Optoelectronic Materials of Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Zhongguancun, Beijing 100190 (China); Liu Chunyan, E-mail: cyliu@mail.ipc.ac.c [Key Laboratory of Photochemical Conversion and Optoelectronic Materials of Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Zhongguancun, Beijing 100190 (China)

2009-12-15T23:59:59.000Z

178

carbon dioxide emissions | OpenEI  

Open Energy Info (EERE)

dioxide emissions dioxide emissions Dataset Summary Description Total annual carbon dioxide emissions by country, 2005 to 2009 (million metric tons). Compiled by Energy Information Administration (EIA). Source EIA Date Released Unknown Date Updated Unknown Keywords carbon dioxide emissions EIA world Data text/csv icon total_carbon_dioxide_emissions_from_the_consumption_of_energy_2005_2009million_metric_tons.csv (csv, 12.3 KiB) Quality Metrics Level of Review Peer Reviewed Comment Temporal and Spatial Coverage Frequency Time Period 2005 - 2009 License License Other or unspecified, see optional comment below Comment Rate this dataset Usefulness of the metadata Average vote Your vote Usefulness of the dataset Average vote Your vote Ease of access Average vote Your vote Overall rating

179

EIA - Greenhouse Gas Emissions - Carbon Dioxide Emissions  

Gasoline and Diesel Fuel Update (EIA)

2. Carbon Dioxide Emissions 2. Carbon Dioxide Emissions 2.1. Total carbon dioxide emissions Annual U.S. carbon dioxide emissions fell by 419 million metric tons in 2009 (7.1 percent), to 5,447 million metric tons (Figure 9 and Table 6). The annual decrease-the largest over the 19-year period beginning with the 1990 baseline-puts 2009 emissions 608 million metric tons below the 2005 level, which is the Obama Administration's benchmark year for its goal of reducing U.S. emissions by 17 percent by 2020. The key factors contributing to the decrease in carbon dioxide emissions in 2009 included an economy in recession with a decrease in gross domestic product of 2.6 percent, a decrease in the energy intensity of the economy of 2.2 percent, and a decrease in the carbon intensity of energy supply of

180

Carbon dioxide disposal in solid form  

SciTech Connect

Coal reserves can provide for the world`s energy needs for centuries. However, coal`s long term use may be severely curtailed if the emission of carbon dioxide into the atmosphere is not eliminated. We present a safe and permanent method of carbon dioxide disposal that is based on combining carbon dioxide chemically with abundant raw materials to form stable carbonate minerals. We discuss the availability of raw materials and potential process designs. We consider our initial rough cost estimate of about 3{cents}/kWh encouraging. The availability of a carbon dioxide fixation technology would serve as insurance in case global warming, or the perception of global warming, causes severe restrictions on carbon dioxide emissions. If the increased energy demand of a growing world population is to be satisfied from coal, the implementation of such a technology would quite likely be unavoidable.

Lackner, K.S.; Butt, D.P.; Sharp, D.H. [Los Alamos National Lab., NM (United States); Wendt, C.H. [Auxon Corp., (United States)

1995-12-31T23:59:59.000Z

Note: This page contains sample records for the topic "dioxide nitrous oxide" 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

NETL: Carbon Dioxide 101 FAQs  

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

is the greenhouse effect? is the greenhouse effect? Greenhouse Effect Greenhouse Effect The greenhouse effect is used to describe the phenomenon whereby the Earth's atmosphere traps solar radiation, caused by the presence of gases, such as carbon dioxide (CO2), methane (CH4), and water vapor (H2O), in the atmosphere that allow incoming sunlight to pass through but absorb heat radiated back from the Earth's surface, resulting in higher temperatures. The greenhouse effect gets its name from what actually happens in a greenhouse. In a greenhouse, short wavelength visible sunlight shines through the glass panes and warms the air and the plants inside. The radiation emitted from the heated objects is of longer wavelength and is unable to pass through the glass barrier, maintaining a warm temperature

182

SEQUESTERING CARBON DIOXIDE IN COALBEDS  

SciTech Connect

The authors' long term goal is to develop accurate prediction methods for describing the adsorption behavior of gas mixtures on solid adsorbents over complete ranges of temperature, pressure and adsorbent types. The major objectives of the project are to: (1) measure the adsorption behavior of pure CO{sub 2}, methane, nitrogen and their binary and ternary mixtures on several selected coals having different properties at temperatures and pressures applicable to the particular coal being studied, (2) generalize the adsorption results in terms of appropriate properties of the coals, to facilitate estimation of adsorption behavior for coals other than those studied experimentally, (3) delineate the sensitivity of the competitive adsorption of CO{sub 2}, methane and nitrogen to the specific characteristics of the coal on which they are adsorbed; establish the major differences (if any) in the nature of this competitive adsorption on different coals, and (4) test and/or develop theoretically-based mathematical models to represent accurately the adsorption behavior of mixtures of the type for which measurements are made. The specific accomplishments of this project during this reporting period are summarized below in three broad categories outlining experimentation, model development, and coal characterization. (1) Experimental Work: Our adsorption apparatus was reassembled, and all instruments were tested and calibrated. Having confirmed the viability of the experimental apparatus and procedures used, adsorption isotherms for pure methane, carbon dioxide and nitrogen on wet Fruitland coal were measured at 319.3 K (115 F) and pressures to 12.4 MPa (1800 psia). These measurements showed good agreement with our previous data and yielded an expected uncertainty of about 2%. Preparations are underway to measure adsorption isotherms for pure methane, carbon dioxide and nitrogen on two other coals. (2) Model Development: The experimental data were used to evaluate the predictive capabilities of various adsorption models, including the Langmuir/loading ratio correlation, two-dimensional cubic equations of state, and the local density model. In general, all models performed well for Type I adsorption exhibited by methane, nitrogen, and carbon dioxide up to 8.3 MPa (average deviations within 2%). However, for pressures higher than 8.3 MPa (1200 psia), carbon dioxide produced multilayer adsorption behavior similar to Type IV adsorption. Our results to date indicate that the SLD model may be a suitable choice for modeling multilayer coalbed gas adsorption. However, model improvements are required to (a) account for coal heterogeneity and structure complexity, and (b) provide for more accurate density predictions. (3) Coal Characterization: We have identified several well-characterized coals for use in our adsorption studies. The criteria for coal selection has been guided by the need for coals that (a) span the spectrum of properties encountered in coalbed methane production (such as variation in rank), and (b) originate from coalbed methane recovery sites (e.g., San Juan Basin, Black Warrior Basin, etc.). At Pennsylvania State University, we have completed calibrating our instruments using a well-characterized activated carbon. In addition, we have conducted CO{sub 2} and methane uptakes on four samples, including (a) a widely used commercial activated carbon, BPL from Calgon Carbon Corp.; (b) an Illinois No.6 bituminous coal from the Argonne Premium Coal sample bank; (c) a Fruitland Intermediate coal sample; (d) a dry Fruitland sample. The results are as expected, except for a greater sensitivity to the outgassing temperature. ''Standard'' outgassing conditions (e.g., 383.2 K, overnight), which are often used, may not be appropriate for gas storage in coalbeds. Conditions that are more representative of in-situ coal (approximately 313.2 K) may be much more appropriate. In addition, our results highlight the importance of assessing the degree of approach to adsorption equilibrium.

K.A.M. Gasem; R.L. Robinson, Jr.; L.R. Radovic

2001-06-15T23:59:59.000Z

183

Superior catalysts for selective catalytic reduction of nitric oxide. Quarterly technical progress report, January 1, 1995--March 31, 1995  

DOE Green Energy (OSTI)

During this quarter, progress was made on the following tasks: TPD techniques were employed to study the reaction mechanism of the selective catalytic reduction of nitrogen oxide with ammonia over iron oxide pillared clay catalyst; and a sulfur dioxide resistant iron oxide/titanium oxide catalyst was developed.

Li, W.B.; Yang, R.T.

1995-12-01T23:59:59.000Z

184

METHOD FOR SEPARATING PLUTONIUM AND FISSION PRODUCTS EMPLOYING AN OXIDE AS A CARRIER FOR FISSION PRODUCTS  

DOE Patents (OSTI)

Carrier precipitation processes for separating plutonium values from uranium fission products are described. Silicon dioxide or titanium dioxide in a finely divided state is added to an acidic aqueous solution containing hexavalent plutonium ions together with ions of uranium fission products. The supernatant solution containing plutonium ions is then separated from the oxide and the fission products associated therewith.

Davies, T.H.

1961-07-18T23:59:59.000Z

185

Winter and summer nitrous oxide and nitrogen oxides fluxes from a seasonally snow-covered subalpine meadow at Niwot Ridge, Colorado  

E-Print Network (OSTI)

of Geography, University of Colorado, Boulder, CO, USA M. W.Alpine Research, University of Colorado, Boulder, CO, USA D.Sciences, University of Colorado, Boulder, CO, USA B. Hall

2009-01-01T23:59:59.000Z

186

Appendix B: CArBon dioxide CApture teChnology SheetS Oxygen PrOductiOn  

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

Oxygen PrOductiOn B-500 Oxygen PrOductiOn u.S. dePartment Of energy advanced carbOn diOxide caPture r&d PrOgram: technOlOgy uPdate, may 2013 itm Oxygen technOlOgy fOr integratiOn...

187

Carbon Dioxide Capture Technology for the Coal-Powered Electricity Industry: A Systematic Prioritization of Research Needs  

E-Print Network (OSTI)

Balbach, J. H. (1991). "Modeling the removal of sulfur dioxide and nitrogen oxides from flue gases using% by volume (Chang et al. 1992b). Such observation is important for combustors that operate with flue gases and ultraviolet radiation. The composition, tem- perature, and pressure of the treated gas streams simulate gases

188

Method for combined removal of mercury and nitrogen oxides from off-gas streams  

DOE Patents (OSTI)

A method for removing elemental Hg and nitric oxide simultaneously from a gas stream is provided whereby the gas stream is reacted with gaseous chlorinated compound to convert the elemental mercury to soluble mercury compounds and the nitric oxide to nitrogen dioxide. The method works to remove either mercury or nitrogen oxide in the absence or presence of each other.

Mendelsohn, Marshall H. (Downers Grove, IL); Livengood, C. David (Lockport, IL)

2006-10-10T23:59:59.000Z

189

Fast-regenerable sulfur dioxide adsorbents for diesel engine emission control  

Science Conference Proceedings (OSTI)

Disclosed herein are sorbents and devices for controlling sulfur oxides emissions as well as systems including such sorbents and devices. Also disclosed are methods for making and using the disclosed sorbents, devices and systems. In one embodiment the disclosed sorbents can be conveniently regenerated, such as under normal exhaust stream from a combustion engine, particularly a diesel engine. Accordingly, also disclosed are combustion vehicles equipped with sulfur dioxide emission control devices.

Li, Liyu [Richland, WA; King, David L [Richland, WA

2011-03-15T23:59:59.000Z

190

Carbon Dioxide Information Analysis Center (CDIAC)  

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

Latest Estimates Latest Estimates Atmos CO2 Level 397.31 ppm Fossil CO2 Emissions 9,167 MMT Carbon Global Temp Anomaly +0.56°C / +1.01°F Global Sea Level Rise +2.9 ± 0.4 mm/y Carbon Dioxide Information Analysis Center The Carbon Dioxide Information Analysis Center (CDIAC) is the primary climate-change data and information analysis center of the U.S. Department of Energy (DOE). CDIAC is located at DOE's Oak Ridge National Laboratory (ORNL) and includes the World Data Center for Atmospheric Trace Gases. CDIAC's data holdings include estimates of carbon dioxide emissions from fossil-fuel consumption and land-use changes; records of atmospheric concentrations of carbon dioxide and other radiatively active trace gases; carbon cycle and terrestrial carbon management datasets and analyses; and

191

Canada, carbon dioxide and the greenhouse effect  

SciTech Connect

One of the major contributors to the greenhouse effect is carbon dioxide from the combustion of fossil fuels such as coal, oil, and natural gas. Even with its low population density, Canada, on a per capita basis, has the dubious distinction of being the world's fourth largest producer of carbon from carbon dioxide. This paper considers the impact of Canadian carbon dioxide emissions on the greenhouse effect in light of the 1988 Conference on the Changing Atmosphere's recommendations. A computer model has been developed that, when using anticipated Canadian fossil fuel demands, shows that unless steps are taken immediately, Canada will not be able to meet the conference's proposed carbon dioxide reduction of 20 percent of 1988 levels by the year 2005, let alone meet any more substantial cuts that may be required in the future.

Hughes, L.; Scott, S. (Dept. of Mathematics and Computing Science, Saint Mary' s Univ., Halifax, Nova Scotia B3H 3C3 (CA))

1991-01-01T23:59:59.000Z

192

Turning unwanted carbon dioxide into electricity  

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

and use it as a tool to boost electric power. Turning unwanted carbon dioxide into electricity Anne M Stark, LLNL, (925) 422-9799, stark8@llnl.gov High Resolution Image The...

193

Sequestration of Carbon Dioxide in Coal Seams  

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

Carbon Dioxide in Coal Seams K. Schroeder (schroede@netl.doe.gov; 412.386.5910) U.S. Department of Energy National Energy Technology Laboratory P.O. Box 10940 Pittsburgh, PA 15236...

194

Carbon Dioxide Variability and Atmospheric Circulation  

Science Conference Proceedings (OSTI)

Hourly values of the concentration of atmospheric carbon dioxide at Mauna Loa Observatory (MLO) formed the basis for an investigation of concentration fluctuations on daily to monthly time scales. In agreement with earlier studies we found no ...

James C. Sadler; Colin S. Ramage; Arnold M. Hori

1982-06-01T23:59:59.000Z

195

Regulating carbon dioxide capture and storage  

E-Print Network (OSTI)

This essay examines several legal, regulatory and organizational issues that need to be addressed to create an effective regulatory regime for carbon dioxide capture and storage ("CCS"). Legal, regulatory, and organizational ...

De Figueiredo, Mark A.

2007-01-01T23:59:59.000Z

196

Carbon Dioxide Emission Factors for Coal  

Reports and Publications (EIA)

The Energy Information Administration (EIA) has developed factors for estimating the amount of carbon dioxide emitted, accounting for differences among coals, to reflect the changing "mix" of coal in U.S. coal consumption.

William Watson

1994-08-01T23:59:59.000Z

197

Biomass burning and the production of greenhouse gases, in Climate Biosphere Interaction: Biogenic Emissions and the Environmental Effects of Climate Change, edited by  

E-Print Network (OSTI)

Biomass burning is a source of greenhouse gases, carbon dioxide, methane, and nitrous oxide. In addition, biomass burning is a source of chemically active gases, including carbon monoxide, nonmethane hydrocarbons, and nitric oxide. These gases, along with methane, lead to the chemical production of tropospheric ozone (another greenhouse gas) as well as control the concentration of the

Joel S. Levine

1994-01-01T23:59:59.000Z

198

Thorium dioxide: properties and nuclear applications  

SciTech Connect

This is the sixth book on reactor materials published under sponsorship of the Naval Reactors Office of the United States Department of Energy, formerly the United States Atomic Energy Commission. This book presents a comprehensive compilation of the most significant properties of thorium dioxide, much like the book Uranium Dioxide: Properties and Nuclear Applications presented information on the fuel material used in the Shippingport Pressurized Water Reactor core.

Belle, J.; Berman, R.M. (eds.)

1984-01-01T23:59:59.000Z

199

Copper mercaptides as sulfur dioxide indicators  

DOE Patents (OSTI)

Organophosphine copper(I) mercaptide complexes are useful as convenient and semiquantitative visual sulfur dioxide gas indicators. The air-stable complexes form 1:1 adducts in the presence of low concentrations of sulfur dioxide gas, with an associated color change from nearly colorless to yellow-orange. The mercaptides are made by mixing stoichiometric amounts of the appropriate copper(I) mercaptide and phosphine in an inert organic solvent.

Eller, Phillip G. (Los Alamos, NM); Kubas, Gregory J. (Los Alamos, NM)

1979-01-01T23:59:59.000Z

200

SEQUESTERING CARBON DIOXIDE IN COALBEDS  

SciTech Connect

During the present reporting period, six complementary tasks involving experimentation, model development, and coal characterization were undertaken to meet our project objectives: (1) A second adsorption apparatus, utilizing equipment donated by BP Amoco, was assembled. Having confirmed the reliability of this additional experimental apparatus and procedures, adsorption isotherms for CO{sub 2}, methane, ethane, and nitrogen on wet Fruitland coal and on activated carbon were measured at 319.3 K (115 F) and pressures to 12.4 MPa (1800 psia). These measurements showed good agreement with our previous data and yielded an expected uncertainty of about 3%. The addition of this new facility has allowed us to essentially double our rate of data production. (2) Adsorption isotherms for pure CO{sub 2}, methane, and nitrogen on wet Illinois-6 coal and on activated carbon were measured at 319.3 K (115 F) and pressures to 12.4 MPa (1800 psia) on our first apparatus. The activated carbon measurements showed good agreement with literature data and with measurements obtained on our second apparatus. The expected uncertainty of the data is about 3%. The Illinois-6 adsorption measurements are a new addition to the existing database. Preparations are underway to measure adsorption isotherms for pure methane, carbon dioxide and nitrogen on DESC-8 coal. (3) Adsorption from binary mixtures of methane, nitrogen and CO{sub 2} at a series of compositions was also measured on the wet Fruitland coal at 319.3 K (115 F), using our first apparatus. The nominal compositions of these mixtures are 20%/80%, 40%/60%, 60%/40%, and 80%/20%. The experiments were conducted at pressures from 100 psia to 1800 psia. The expected uncertainty for these binary mixture data varies from 2 to 9%. (4) A study was completed to address the previously-reported rise in the CO{sub 2} absolute adsorption on wet Fruitland coal at 115 F and pressures exceeding 1200 psia. Our additional adsorption measurements on Fruitland coal and on activated carbon show that: (a) the Gibbs adsorption isotherm for CO{sub 2} under study exhibits typical adsorption behavior for supercritical gas adsorption, and (b) a slight variation from Type I absolute adsorption may be observed for CO{sub 2}, but the variation is sensitive to the estimates used for adsorbed phase density. (5) The experimental data were used to evaluate the predictive capabilities of various adsorption models, including the Langmuir/loading ratio correlation, a two-dimensional cubic equation of state (EOS), a new two-dimensional (2-D) segment-segment interactions equation of state, and the simplified local density model (SLD). Our model development efforts have focused on developing the 2-D analog to the Park-Gasem-Robinson (PGR) EOS and an improved form of the SLD model. The new PGR EOS offers two advantages: (a) it has a more accurate repulsive term, which is important for reliable adsorption predictions, and (b) it is a segment-segment interactions model, which should more closely describe the gas-coal interactions during the adsorption process. In addition, a slit form of the SLD model was refined to account more precisely for heterogeneity of the coal surface and matrix swelling. In general, all models performed well for the Type I adsorption exhibited by methane, nitrogen, and carbon dioxide up to 8.3 MPa (average deviations within 2%). In comparison, the SLD model represented the adsorption behavior of all fluids considered within 5% average deviations, including the near-critical behavior of carbon dioxide beyond 8.3 MPa (1200 psia). Work is in progress to (a) derive and implement the biporous form of the SLD model, which would expand the number of structural geometries used to represent the heterogeneity of coal surface; and (b) extend the SLD model to mixture predictions. (6) Proper reduction of our adsorption data requires accurate gas-phase compressibility (Z) factors for methane, ethane, nitrogen and carbon dioxide and their mixtures to properly analyze our experimental adsorption data. A careful evaluation of t

K.A.M. Gasem; R.L. Robinson, Jr.; L.R. Radovic

2001-06-15T23:59:59.000Z

Note: This page contains sample records for the topic "dioxide nitrous oxide" 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

Energy and Air Emission Implications of a Decentralized Wastewater System  

E-Print Network (OSTI)

Carbon monoxide; CO 2 (e): Carbon dioxide equivalent; NO x :Darby J L, 2011. Methane, Carbon Dioxide, and Nitrous Oxidemethane biogas to carbon dioxide, a conversion efficiency of

Shehabi, Arman

2013-01-01T23:59:59.000Z

202

Energy Information Handbook: Applications for Energy-Efficient Building Operations  

E-Print Network (OSTI)

coefficients for carbon dioxide, methane, and nitrous oxideinternational standard of carbon dioxide equivalent (CO 2Carbon Equivalents and Carbon Dioxide Equivalents. February

Granderson, Jessica

2013-01-01T23:59:59.000Z

203

Increased Cytotoxicity of Oxidized Flame Soot  

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

Increased Cytotoxicity of Oxidized Flame Soot Increased Cytotoxicity of Oxidized Flame Soot Title Increased Cytotoxicity of Oxidized Flame Soot Publication Type Journal Article Year of Publication 2012 Authors Holder, Amara L., Brietta J. Carter, Regine Goth-Goldstein, Donald Lucas, and Catherine P. Koshland Journal Atmospheric Pollution Research Volume 3 Start Page 25 Issue 1 Pagination 25-31 Date Published 01/2012 Keywords health effects, ozone, soot, toxicity Abstract Combustion-generated particles released into the atmosphere undergo reactions with oxidants, which can change the particles' physiochemical characteristics. In this work, we compare the physical and chemical properties and cellular response of particles fresh from a flame with those oxidized by ozone and nitrogen dioxide. The reaction with ozone and nitrogen dioxide does not significantly modify the physical characteristics of the particles (primary particle size, fractal dimension, and surface area). However, oxidation affects the chemical characteristics of the particles, creating more oxygen and nitrogen containing functional groups, and increases their hydrophilicity. In addition, oxidized soot generates more reactive oxygen species, as measured by the dithiothreitol (DTT) assay. Furthermore, oxidized soot is 1.5-2 times more toxic than soot that was not reacted with ozone, but the inflammatory response, measured by interleukin-8 (IL-8) secretion, is unchanged. These results imply that combustion-generated particles released into the atmosphere will have an increased toxicity on or after high ozone days.

204

Ceramic coating system or water oxidation environments  

DOE Patents (OSTI)

A process for water oxidation of combustible materials in which during at least a part of the oxidation corrosive material is present and makes contact with at least a portion of the apparatus over a contact area on the apparatus. At least a portion of the contact surface area comprises titanium dioxide coated onto a titanium metal substrate. Such ceramic composites have been found to be highly resistant to environments encountered in the process of supercritical water oxidation. Such environments typically contain greater than 50 mole percent water, together with oxygen, carbon dioxide, and a wide range of acids, bases, and salts. Pressures are typically about 27.5 to about 1000 bar while temperatures range as high as 700.degree. C. The ceramic composites are also resistant to degradation mechanisms caused by thermal stresses.

Hong, Glenn T. (Tewksbury, MA)

1996-01-01T23:59:59.000Z

205

Electrocatalytic reduction of carbon dioxide to carbon monoxide by rhenium and manganese polypyridyl catalysts  

E-Print Network (OSTI)

for reduction of carbon dioxide. IR-SpectroelectrochemicalElectrocatalytic reduction of carbon dioxide mediated by Re(Reduction of Carbon Dioxide to Carbon Monoxide Mediated by (

Smieja, Jonathan Mark

2012-01-01T23:59:59.000Z

206

Thermal dissociation behavior and dissociation enthalpies of methane-carbon dioxide mixed hydrates  

E-Print Network (OSTI)

of Methane– Title: Carbon Dioxide Mixed Hydrates Tae-Hyukof methane with carbon dioxide in hydrate has been proposedsequestration of carbon dioxide ( CO 2 ) and/or production

Kwon, T.H.

2012-01-01T23:59:59.000Z

207

Oil shale oxidation at subretorting temperatures  

SciTech Connect

Green River oil shale was air oxidized at subretorting temperatures. Off gases consisting of nitrogen, oxygen, carbon monoxide, carbon dioxide, and water were monitored and quantitatively determined. A mathematical model of the oxidation reactions based on a shrinking core model has been developed. This model incorporates the chemical reaction of oxygen and the organic material in the oil shale as well as the diffusivity of the oxygen into the shale particle. Diffusivity appears to be rate limiting for the oxidation. Arrhenius type equations, which include a term for oil shale grade, have been derived for both the chemical reaction and the diffusivity.

Jacobson, I.A. Jr.

1980-06-01T23:59:59.000Z

208

Vehicle Technologies Office: Fact #464: April 9, 2007 Carbon Dioxide  

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

4: April 9, 2007 4: April 9, 2007 Carbon Dioxide Emissions to someone by E-mail Share Vehicle Technologies Office: Fact #464: April 9, 2007 Carbon Dioxide Emissions on Facebook Tweet about Vehicle Technologies Office: Fact #464: April 9, 2007 Carbon Dioxide Emissions on Twitter Bookmark Vehicle Technologies Office: Fact #464: April 9, 2007 Carbon Dioxide Emissions on Google Bookmark Vehicle Technologies Office: Fact #464: April 9, 2007 Carbon Dioxide Emissions on Delicious Rank Vehicle Technologies Office: Fact #464: April 9, 2007 Carbon Dioxide Emissions on Digg Find More places to share Vehicle Technologies Office: Fact #464: April 9, 2007 Carbon Dioxide Emissions on AddThis.com... Fact #464: April 9, 2007 Carbon Dioxide Emissions Carbon dioxide (CO2) emissions from the transportation sector began to

209

Simultaneous removal of nitrogen oxides and sulfur oxides from combustion gases  

DOE Patents (OSTI)

A process for the simultaneous removal of sulfur oxides and nitrogen oxides from power plant stack gases comprising contacting the stack gases with a supported iron oxide catalyst/absorbent in the presence of sufficient reducing agent selected from the group consisting of carbon monoxide, hydrogen, and mixtures thereof, to provide a net reducing atmosphere in the SO.sub.x /NO.sub.x removal zone. The sulfur oxides are removed by absorption substantially as iron sulfide, and nitrogen oxides are removed by catalytic reduction to nitrogen and ammonia. The spent iron oxide catalyst/absorbent is regenerated by oxidation and is recycled to the contacting zone. Sulfur dioxide is also produced during regeneration and can be utilized in the production of sulfuric acid and/or sulfur.

Clay, David T. (Longview, WA); Lynn, Scott (Walnut Creek, CA)

1976-10-19T23:59:59.000Z

210

The sacrificial oxide etching of poly-Si cantilevers having high aspect ratios using supercritical CO2  

Science Conference Proceedings (OSTI)

The aqueous etchants used in conventional wet etching for the micromachining of integrated circuits and MEMS devices often encumber the processes with a stiction problem. A dry etching method with anhydrous HF/pyridine in supercritical carbon dioxide ... Keywords: Cantilever, Etching, MEMS, Poly-Si, Sacrificial oxide, Supercritical carbon dioxide

Ha Soo Hwang; Jae Hyun Bae; Jae Mok Jung; Kwon Taek Lim

2010-11-01T23:59:59.000Z

211

SEQUESTERING CARBON DIOXIDE IN COALBEDS  

SciTech Connect

The authors' long-term goal is to develop accurate prediction methods for describing the adsorption behavior of gas mixtures on solid adsorbents over complete ranges of temperature, pressure and adsorbent types. The originally-stated, major objectives of the current project are to (1) measure the adsorption behavior of pure CO{sub 2}, methane, nitrogen, and their binary and ternary mixtures on several selected coals having different properties at temperatures and pressures applicable to the particular coals being studied, (2) generalize the adsorption results in terms of appropriate properties of the coals to facilitate estimation of adsorption behavior for coals other than those studied experimentally, (3) delineate the sensitivity of the competitive adsorption of CO{sub 2}, methane and nitrogen to the specific characteristics of the coal on which they are adsorbed; establish the major differences (if any) in the nature of this competitive adsorption on different coals, and (4) test and/or develop theoretically-based mathematical models to represent accurately the adsorption behavior of mixtures of the type for which measurements are made. As this project has developed, an important additional objective has been added to the above original list. Namely, we have been encouraged to interact with industry and/or governmental agencies to utilize our expertise to advance the state of the art in coalbed adsorption science and technology. As a result of this additional objective, we have participated with the Department of Energy and industry in the measurement and analysis of adsorption behavior as part of two distinct investigations. These include (a) Advanced Resources International (ARI) DOE Project DE-FC26-00NT40924, ''Adsorption of Pure Methane, Nitrogen, and Carbon Dioxide and Their Mixtures on Wet Tiffany Coal'', and (b) the DOE-NETL Project, ''Round Robin: CO{sub 2} Adsorption on Selected Coals''. These activities, contributing directly to the DOE projects listed above, have also provided direct synergism with the original goals of our work. Specific accomplishments of this project during the current reporting period are summarized in three broad categories outlining experimentation, model development, and coal characterization.

K.A.M. Gasem; R.L. Robinson, Jr.; L.R. Radovic

2003-03-10T23:59:59.000Z

212

SEQUESTERING CARBON DIOXIDE IN COALBEDS  

SciTech Connect

The authors' long-term goal is to develop accurate prediction methods for describing the adsorption behavior of gas mixtures on solid adsorbents over complete ranges of temperature, pressure, and adsorbent types. The originally-stated, major objectives of the current project are to: (1) measure the adsorption behavior of pure CO{sub 2}, methane, nitrogen, and their binary and ternary mixtures on several selected coals having different properties at temperatures and pressures applicable to the particular coals being studied, (2) generalize the adsorption results in terms of appropriate properties of the coals to facilitate estimation of adsorption behavior for coals other than those studied experimentally, (3) delineate the sensitivity of the competitive adsorption of CO{sub 2}, methane, and nitrogen to the specific characteristics of the coal on which they are adsorbed; establish the major differences (if any) in the nature of this competitive adsorption on different coals, and (4) test and/or develop theoretically-based mathematical models to represent accurately the adsorption behavior of mixtures of the type for which measurements are made. As this project developed, an important additional objective was added to the above original list. Namely, we were encouraged to interact with industry and/or governmental agencies to utilize our expertise to advance the state of the art in coalbed adsorption science and technology. As a result of this additional objective, we participated with the Department of Energy and industry in the measurement and analysis of adsorption behavior as part of two distinct investigations. These include (a) Advanced Resources International (ARI) DOE Project DE-FC26-00NT40924, ''Adsorption of Pure Methane, Nitrogen, and Carbon Dioxide and Their Mixtures on Wet Tiffany Coal'', and (b) the DOE-NETL Project, ''Round Robin: CO{sub 2} Adsorption on Selected Coals''. These activities, contributing directly to the DOE projects listed above, also provided direct synergism with the original goals of our work. Specific accomplishments of this project are summarized below in three broad categories: experimentation, model development, and coal characterization.

K.A.M. Gasem; R.L. Robinson, Jr.; J.E. Fitzgerald; Z. Pan; M. Sudibandriyo

2003-04-30T23:59:59.000Z

213

A Vortex Contactor for Carbon Dioxide Separations  

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

Vortex Contactor for Carbon Dioxide Separations Vortex Contactor for Carbon Dioxide Separations Kevin T. Raterman (ratekt@inel.gov; 208-526-5444) Michael McKellar (mgq@inel.gov; 208-526-1346) Anna Podgorney (poloak@inel.gov; 208-526-0064) Douglas Stacey (stacde@inel.gov; 208-526-3938) Terry Turner (tdt@inel.gov; 208-526-8623) Idaho National Engineering and Environmental Laboratory P.O. Box 1625 Idaho Falls, Idaho 83415-2110 Brian Stokes (bxs9@pge.com; 415-972-5591) John Vranicar (jjv2@pge.com; 415-972-5591) Pacific Gas & Electric Company 123 Mission Street San Francisco, CA 94105 Introduction Many analysts 1,2,3 identify carbon dioxide (CO 2 ) capture and separation as a major roadblock in efforts to cost effectively mitigate greenhouse gas emissions via sequestration. An assessment 4 conducted by the International Energy Agency (IEA)

214

Polymers for metal extractions in carbon dioxide  

DOE Patents (OSTI)

A composition useful for the extraction of metals and metalloids comprises (a) carbon dioxide fluid (preferably liquid or supercritical carbon dioxide); and (b) a polymer in the carbon dioxide, the polymer having bound thereto a ligand that binds the metal or metalloid; with the ligand bound to the polymer at a plurality of locations along the chain length thereof (i.e., a plurality of ligands are bound at a plurality of locations along the chain length of the polymer). The polymer is preferably a copolymer, and the polymer is preferably a fluoropolymer such as a fluoroacrylate polymer. The extraction method comprises the steps of contacting a first composition containing a metal or metalloid to be extracted with a second composition, the second composition being as described above; and then extracting the metal or metalloid from the first composition into the second composition.

DeSimone, Joseph M. (7315 Crescent Ridge Dr., Chapel Hill, NC 27516); Tumas, William (1130 Big Rock Loop, Los Alamos, NM 87544); Powell, Kimberly R. (103 Timber Hollow Ct. Apartment 323, Chapel Hill, NC 27514); McCleskey, T. Mark (1930 Camino Mora, Los Alamos, NM 87544); Romack, Timothy J. (5810 Forest Ridge Dr., Durham, NC 27713); McClain, James B. (8530 Sommersweet La., Raleigh, NC 27612); Birnbaum, Eva R. (1930 Camino Mora, Los Alamos, NM 87544)

2001-01-01T23:59:59.000Z

215

CHLORINE DIOXIDE AND CHLORITE Chlorine Dioxide CAS # 10049-04-4  

E-Print Network (OSTI)

This fact sheet answers the most frequently asked health questions (FAQs) about chlorine dioxide and chlorite. For more information, call the ATSDR Information Center at 1-888-422-8737. This fact sheet is one in a series of summaries about hazardous substances and their health effects. It is important you understand this information because these substances may harm you. The effects of exposure to any hazardous substance depend on the dose, the duration, how you are exposed, personal traits and habits, and whether other chemicals are present. HIGHLIGHTS: Chlorine dioxide is a gas that does not occur naturally in the environment. It is used to disinfect drinking water and make it safe to drink. Chlorite is formed when chlorine dioxide reacts with water. High levels of chlorine dioxide can be irritating to the nose, eyes, throat, and lungs. Chlorine dioxide and chlorite have not been found in any of the 1,647 National Priorities List sites identified by the Environmental Protection Agency (EPA). What are chlorine dioxide and chlorite? Chlorine dioxide is a yellow to reddish-yellow manufactured gas. It does not occur naturally in the environment. When

Chlorite Cas

2004-01-01T23:59:59.000Z

216

Magnesium/manganese dioxide electrochemical cell  

SciTech Connect

This patent describes an improvement in a magnesium/manganese dioxide electrochemical cell that has been stored following partial usage and including an alloy of magnesium as the anode, a moist cathode mix of carbon black, manganese dioxide, magnesium hydroxide, barium chromate and lithium chromate as the cathode, and 3.5 to 4.0 normal magnesium perchlorate as the electrolyte. The improvement involves increasing the moisture content of the cathode mix from 34 to 38 percent at the time of making the cell to reduce the self discharge and increase the operating capacity after the cell has been stored following partial usage.

Jarvis, L.P.; Brundage, M.T.; Atwater, T.B.

1989-09-26T23:59:59.000Z

217

Fabrication of Cerium Oxide and Uranium Oxide Microspheres for Space Nuclear Power Applications  

Science Conference Proceedings (OSTI)

Cerium oxide and uranium oxide microspheres are being produced via an internal gelation sol-gel method to investigate alternative fabrication routes for space nuclear fuels. Depleted uranium and non-radioactive cerium are being utilized as surrogates for plutonium-238 (Pu-238) used in radioisotope thermoelectric generators and for enriched uranium required by nuclear thermal rockets. While current methods used to produce Pu-238 fuels at Los Alamos National Laboratory (LANL) involve the generation of fine powders that pose a respiratory hazard and have a propensity to contaminate glove boxes, the sol-gel route allows for the generation of oxide microsphere fuels through an aqueous route. The sol-gel method does not generate fine powders and may require fewer processing steps than the LANL method with less operator handling. High-quality cerium dioxide microspheres have been fabricated in the desired size range and equipment is being prepared to establish a uranium dioxide microsphere production capability.

Jeffrey A. Katalenich; Michael R. Hartman; Robert C. O'Brien

2013-02-01T23:59:59.000Z

218

EIA - International Energy Outlook 2008-Energy-Related Carbon Dioxide  

Gasoline and Diesel Fuel Update (EIA)

Energy-Related Carbon Dioxide Emissions Energy-Related Carbon Dioxide Emissions International Energy Outlook 2008 Chapter 7 - Energy-Related Carbon Dioxide Emissions In 2005, non-OECD emissions of carbon dioxide exceeded OECD emissions by 7 percent. In 2030, carbon dioxide emissions from the non-OECD countries are projected to exceed those from the OECD countries by 72 percent. Figure 75. World Energy-Related Carbon Dioxide Emissions, 2005-2030 (Billion Metric Tons). Need help, contact the National Energy Information Center at 202-586-8800. Figure Data Figure 76. World Energy-Related Carbon Dioxide Emissions by Fuel Type, 1990-2030 (Billion Metric Tons). Need help, contact the National Energy Information Center at 202-586-8800. Figure Data Figure 77. Average Annual Growth in Energy-Related Carbon Dioxide Emissions in the OECD Economies, 2005-2030 (Percent per Year). Need help, contact the National Energy Information Center at 202-586-8800.

219

Dry process fluorination of uranium dioxide using ammonium bifluoride  

E-Print Network (OSTI)

An experimental study was conducted to determine the practicality of various unit operations for fluorination of uranium dioxide. The objective was to prepare ammonium uranium fluoride double salts from uranium dioxide and ...

Yeamans, Charles Burnett, 1978-

2003-01-01T23:59:59.000Z

220

New Texas Oil Project Will Help Keep Carbon Dioxide Underground...  

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

Texas Oil Project Will Help Keep Carbon Dioxide Underground New Texas Oil Project Will Help Keep Carbon Dioxide Underground February 5, 2013 - 12:05pm Addthis The Air Products and...

Note: This page contains sample records for the topic "dioxide nitrous oxide" 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

How much carbon dioxide is produced by burning gasoline and ...  

U.S. Energy Information Administration (EIA)

How much carbon dioxide is produced by burning gasoline and diesel fuel? About 19.64 pounds of carbon dioxide (CO 2) are produced from burning a gallon of gasoline ...

222

Recycling Carbon Dioxide to Make Plastics | Department of Energy  

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

Recycling Carbon Dioxide to Make Plastics Recycling Carbon Dioxide to Make Plastics May 20, 2013 - 1:31pm Addthis Novomers thermoplastic pellets incorporate waste CO2 into a...

223

Carbon Dioxide Capture/Sequestration Tax Deduction (Kansas)  

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

Carbon Dioxide Capture/Sequestration Tax Deduction allows a taxpayer a deduction to adjusted gross income with respect to the amortization of the amortizable costs of carbon dioxide capture,...

224

Calculating Residential Carbon Dioxide Emissions --A New Approach  

E-Print Network (OSTI)

Calculating Residential Carbon Dioxide Emissions -- A New Approach Larry Hughes, Kathleen Bohan to submit an annual national greenhouse gas inventory to the United Nations Framework Convention on Climate different sectors and their associated greenhouse gas emissions (principally carbon dioxide, methane

Hughes, Larry

225

Fluid Dynamics of Carbon Dioxide Disposal into Saline Aquifers  

E-Print Network (OSTI)

carbon dioxide can be less than the viscosity of the aqueous phase by a factorcarbon dioxide can be less than the viscosity of the aqueous phase by a factor

Garcia, Julio Enrique

2003-01-01T23:59:59.000Z

226

EIA - International Energy Outlook 2007 - Energy-Related Carbon Dioxide  

Gasoline and Diesel Fuel Update (EIA)

Energy-Relaated Carbon Dioxide Emissions Energy-Relaated Carbon Dioxide Emissions International Energy Outlook 2007 Chapter 7 - Energy-Related Carbon Dioxide Emissions In 2004, non-OECD emissions of carbon dioxide were greater than OECD emissions for the first time. In 2030, carbon dioxide emissions from the non-OECD countries are projected to exceed those from the OECD countries by 57 percent. Figure 77. World Energy-Related Carbon Dioxide Emissions by Region, 2003-2030 (Billion Metric Tons). Need help, contact the National Energy Information Center on 202-585-8800. Figure Data Figure 78. World energy-Related Carbon Dioxide Emissions by Fuel Type, 1990-2030 (Billion Metric Tons). Need help, contact the National Energy at 202-586-8800. Figure Data Carbon dioxide is the most abundant anthropogenic (human-caused) greenhouse

227

Energy use and carbon dioxide emissions in energy-intensive industries in key developing countries  

E-Print Network (OSTI)

Structural Factors Affecting Energy Use and Carbon DioxideStructural Factors Affecting Energy Use and Carbon Dioxide

Price, Lynn; Worrell, Ernst; Phylipsen, Dian

1999-01-01T23:59:59.000Z

228

Carbon Dioxide as Cushion Gas for Natural Gas Storage  

Carbon dioxide injection during carbon sequestration with enhanced gas recovery can be carried out to produce the methane while

229

Carbon Dioxide and Other Greenhouse Gas Reduction Metallurgy  

Science Conference Proceedings (OSTI)

About this Symposium. Meeting, 2011 TMS Annual Meeting & Exhibition. Symposium, Carbon Dioxide and Other Greenhouse Gas Reduction Metallurgy - 2011.

230

FLAME DENITRATION AND REDUCTION OF URANIUM NITRATE TO URANIUM DIOXIDE  

DOE Patents (OSTI)

A process is given for converting uranyl nitrate solution to uranium dioxide. The process comprises spraying fine droplets of aqueous uranyl nitrate solution into a hightemperature hydrocarbon flame, said flame being deficient in oxygen approximately 30%, retaining the feed in the flame for a sufficient length of time to reduce the nitrate to the dioxide, and recovering uranium dioxide. (AEC)

Hedley, W.H.; Roehrs, R.J.; Henderson, C.M.

1962-06-26T23:59:59.000Z

231

Cation Adsorption on Manganese Dioxide Impregnated Fibers  

Science Conference Proceedings (OSTI)

The complete removal of radioactive cations by standard mixed-bed ion-exchange resins is sometimes not achieved in liquid radwaste systems. This report documents an alternative ion adsorption process for the purification of liquid wastes, specifically, the use of manganese dioxide (MnO2) impregnated fibers to remove selected cations from PWR liquid waste streams.

1993-02-26T23:59:59.000Z

232

Synthetic fuels, carbon dioxide and climate  

Science Conference Proceedings (OSTI)

The observed increase in atmospheric carbon dioxide (CO2) has been attributed to the use of fossil fuels. There is concern that the generation and use of synthetic fuels derived from oil shale and coal will accelerate the increase of CO2.

Alex R. Sapre; John R. Hummel; Ruth A. Reck

1982-01-01T23:59:59.000Z

233

Carbon Dioxide Capture from Coal-Fired  

E-Print Network (OSTI)

Carbon Dioxide Capture from Coal-Fired Power Plants: A Real Options Analysis May 2005 MIT LFEE 2005. LFEE 2005-002 Report #12;#12;i ABSTRACT Investments in three coal-fired power generation technologies environment. The technologies evaluated are pulverized coal (PC), integrated coal gasification combined cycle

234

Improved magnesium/manganese dioxide electrochemical cell  

SciTech Connect

A magnesium/manganese dioxide electrochemical cell, stored following partial usage, is improved by increasing the cathode moisture content at the time of making the cell to reduce the self-discharge and increase the operating capacity after the cell has been stored following partial usage.

Jarvis, L.P.; Brundage, M.T.; Atwater, T.B.

1988-11-10T23:59:59.000Z

235

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

236

Recovery Act: Carbon Dioxide-Water Emulsion for Enhanced Oil Recovery and Permanent Sequestration of Carbon Dioxid  

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

Carbon Dioxide-Water Carbon Dioxide-Water Emulsion for Enhanced Oil Recovery and Permanent Sequestration of Carbon Dioxide Background The U.S. Department of Energy (DOE) distributed a portion of American Recovery and Reinvestment Act (ARRA) funds to advance technologies for chemical conversion of carbon dioxide (CO 2 ) captured from industrial sources. The focus of the research projects is permanent sequestration of CO 2 through mineralization or development

237

DOE Hydrogen Analysis Repository: Carbon Dioxide Compression, Transport,  

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

Carbon Dioxide Compression, Transport, and Storage Carbon Dioxide Compression, Transport, and Storage Project Summary Full Title: Techno-Economic Models for Carbon Dioxide Compression, Transport, and Storage & Correlations for Estimating Carbon Dioxide Density and Viscosity Project ID: 195 Principal Investigator: David McCollum Brief Description: This project addresses several components of carbon capture and storage (CCS) costs, provides technical models for determining the engineering and infrastructure requirements of CCS, and describes some correlations for estimating CO2 density and viscosity. Keywords: Pipeline, transportation, greenhouse gases (GHG), costs, technoeconomic analysis Purpose Estimate costs of carbon dioxide capture, compression, transport, storage, etc., and provide some technical models for determining the engineering and

238

SunShot Initiative: 10-Megawatt Supercritical Carbon Dioxide Turbine  

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

10-Megawatt Supercritical Carbon 10-Megawatt Supercritical Carbon Dioxide Turbine to someone by E-mail Share SunShot Initiative: 10-Megawatt Supercritical Carbon Dioxide Turbine on Facebook Tweet about SunShot Initiative: 10-Megawatt Supercritical Carbon Dioxide Turbine on Twitter Bookmark SunShot Initiative: 10-Megawatt Supercritical Carbon Dioxide Turbine on Google Bookmark SunShot Initiative: 10-Megawatt Supercritical Carbon Dioxide Turbine on Delicious Rank SunShot Initiative: 10-Megawatt Supercritical Carbon Dioxide Turbine on Digg Find More places to share SunShot Initiative: 10-Megawatt Supercritical Carbon Dioxide Turbine on AddThis.com... Concentrating Solar Power Systems Components Competitive Awards CSP Research & Development Thermal Storage CSP Recovery Act Baseload CSP SunShot Multidisciplinary University Research Initiative

239

International Energy Outlook 2006 - Energy-Related Carbon Dioxide Emissions  

Gasoline and Diesel Fuel Update (EIA)

Eneregy-Related Carbon Dioxide Emissions Eneregy-Related Carbon Dioxide Emissions International Energy Outlook 2006 Chapter 7: Energy-Related Carbon Dioxide Emissions In the coming decades, actions to limit greenhouse gas emissions could affect patterns of energy use around the world and alter the level and composition of energy-related carbon dioxide emissions by energy source. Figure 65. World Carbon Dioxide Emissions by Region, 1990-2030 (Billion Metric Tons). Need help, contact the National Energy Information Center at 202-586-8800. Figure Data Figure 66. World Carbon Dioxide Emissions by Fuel Type, 1980-2030 (Billion Metric Tons). Need help, contact the National Energy Information Center at 202-586-8800. Figure Data Carbon dioxide is one of the most prevalent greenhouse gases in the

240

EIA - 2010 International Energy Outlook - Energy-Related Carbon Dioxide  

Gasoline and Diesel Fuel Update (EIA)

Energy-Related Carbon Dioxide Emissions Energy-Related Carbon Dioxide Emissions International Energy Outlook 2010 Energy-Related Carbon Dioxide Emissions In 2007, non-OECD energy-related emissions of carbon dioxide exceeded OECD emissions by 17 percent. In the IEO2010 Reference case, energy-related carbon dioxide emissions from non-OECD countries in 2035 are about double those from OECD countries. Overview Because anthropogenic emissions of carbon dioxide result primarily from the combustion of fossil fuels, world energy use continues to be at the center of the climate change debate. In the IEO2010 Reference case, world energy-related carbon dioxide emissions29 grow from 29.7 billion metric tons in 2007 to 33.8 billion metric tons in 2020 and 42.4 billion metric tons in 2035 (Table 18).30

Note: This page contains sample records for the topic "dioxide nitrous oxide" 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

Multifunctional Oxides  

Science Conference Proceedings (OSTI)

3) Electric, ferroelectric, magnetic and photonic properties of oxides 4) Theoretical modeling of epitaxial growth, interfaces and microstructures 5) Composition ...

242

The effect of plutonium dioxide water surface coverage on the generation of hydrogen and oxygen  

DOE Green Energy (OSTI)

The conditions for the production of oxygen during radiolysis of water adsorbed onto plutonium dioxide powder are discussed. Studies in the literature investigating the radiolysis of water show that both oxygen and hydrogen can be generated from water adsorbed on high-purity plutonium dioxide powder. These studies indicate that there is a threshold in the amount of water below which oxygen is not generated. The threshold is associated with the number of monolayers of adsorbed water and is shown to occur at approximately two monolayers of molecularly adsorbed water. Material in equilibrium with 50% relative humidity (RH) will be at the threshold for oxygen generation. Using two monolayers of molecularly adsorbed water as the threshold for oxygen production, the total pressure under various conditions is calculated assuming stoichiometric production of hydrogen and oxygen. The specific surface area of the oxide has a strong effect on the final partial pressure. The specific surface areas resulting in the highest pressures within a 3013 container are evaluated. The potential for oxygen generation is mitigated by reduced relative humidity, and hence moisture adsorption, at the oxide surface which occurs if the oxide is warmer than the ambient air. The potential for oxygen generation approaches zero as the temperature difference between the ambient air and the material approaches 6 C.

Veirs, Douglas K. [Los Alamos National Laboratory; Berg, John M. [Los Alamos National Laboratory; Crowder, Mark L. [Savannah River National Laboratory

2012-06-20T23:59:59.000Z

243

www.defra.gov.uk SMALL BUSINESS USER GUIDE  

E-Print Network (OSTI)

is caused by the release of greenhouse gases into the atmosphere. What are greenhouse gas emissions? The key greenhouse gas emissions are carbon dioxide, methane and nitrous oxide hydrofluorocarbons, perfluorocarbons gas emissions? Human activities release greenhouse gas emissions into the atmosphere ­ using

244

Finding Answers to Definition Questions Using Web Knowledge Bases  

E-Print Network (OSTI)

, Information and Computation, pages 484­492 #12;supposed to be the consequence between the greenhouse gas is the greenhouse gas? Answer 1 Greenhouse gas is a kind of gas that causes greenhouse effect. Answer 2 Greenhouse gases include carbon dioxide, methane, nitrous oxide, etc.. Questions like "What is the greenhouse gas

245

Emissions of greenhouse gases in the United States 1995  

Science Conference Proceedings (OSTI)

This is the fourth Energy Information Administration (EIA) annual report on US emissions of greenhouse gases. This report presents estimates of US anthropogenic (human-caused) emissions of carbon dioxide, methane, nitrous oxide, and several other greenhouse gases for 1988 through 1994. Estimates of 1995 carbon dioxide, nitrous oxide, and halocarbon emissions are also provided, although complete 1995 estimates for methane are not yet available. Emissions of carbon dioxide increased by 1.9% from 1993 to 1994 and by an additional 0.8% from 1994 to 1995. Most carbon dioxide emissions are caused by the burning of fossil fuels for energy consumption, which is strongly related to economic growth, energy prices, and weather. The US economy grew rapidly in 1994 and slowed in 1995. Estimated emissions of methane increased slightly in 1994, as a result of a rise in emissions from energy and agricultural sources. Estimated nitrous oxide emissions increased by 1.8% in 1995, primarily due to increased use of nitrogen fertilizers and higher output of chemicals linked to nitrous oxide emissions. Estimated emissions of hydrofluorocarbons (HFCs) and perfluorocarbons (PFCs), which are known to contribute to global warming, increased by nearly 11% in 1995, primarily as a result of increasing substitution for chlorofluorocarbons (CFCs). With the exception of methane, the historical emissions estimates presented in this report are only slightly revised from those in last year`s report.

NONE

1996-10-01T23:59:59.000Z

246

An Intercomparison of Ground-Based Solar FTIR Measurements of Atmospheric Gases at Eureka, Canada  

Science Conference Proceedings (OSTI)

The authors report the results of an intercomparison of vertical column amounts of hydrogen chloride (HCl), hydrogen fluoride (HF), nitrous oxide (N2O), nitric acid (HNO3), methane (CH4), ozone (O3), carbon dioxide (CO2), and nitrogen (N2) ...

C. Paton-Walsh; R. L. Mittermeier; W. Bell; H. Fast; N. B. Jones; A. Meier

2008-11-01T23:59:59.000Z

247

Solid oxide electrochemical reactor science.  

DOE Green Energy (OSTI)

Solid-oxide electrochemical cells are an exciting new technology. Development of solid-oxide cells (SOCs) has advanced considerable in recent years and continues to progress rapidly. This thesis studies several aspects of SOCs and contributes useful information to their continued development. This LDRD involved a collaboration between Sandia and the Colorado School of Mines (CSM) ins solid-oxide electrochemical reactors targeted at solid oxide electrolyzer cells (SOEC), which are the reverse of solid-oxide fuel cells (SOFC). SOECs complement Sandia's efforts in thermochemical production of alternative fuels. An SOEC technology would co-electrolyze carbon dioxide (CO{sub 2}) with steam at temperatures around 800 C to form synthesis gas (H{sub 2} and CO), which forms the building blocks for a petrochemical substitutes that can be used to power vehicles or in distributed energy platforms. The effort described here concentrates on research concerning catalytic chemistry, charge-transfer chemistry, and optimal cell-architecture. technical scope included computational modeling, materials development, and experimental evaluation. The project engaged the Colorado Fuel Cell Center at CSM through the support of a graduate student (Connor Moyer) at CSM and his advisors (Profs. Robert Kee and Neal Sullivan) in collaboration with Sandia.

Sullivan, Neal P. (Colorado School of Mines, Golden, CO); Stechel, Ellen Beth; Moyer, Connor J. (Colorado School of Mines, Golden, CO); Ambrosini, Andrea; Key, Robert J. (Colorado School of Mines, Golden, CO)

2010-09-01T23:59:59.000Z

248

Carbon Dioxide Capture Process with Regenerable Sorbents  

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

Dioxide Capture Process with Regenerable Sorbents Dioxide Capture Process with Regenerable Sorbents sorbent material. Additionally, the design of the system incorporates a cross- flow moving-bed reactor where the gas flows horizontally through a "panel" of solid sorbent that is slowly moving down-wards under gravity flow. With the expanded use of fossil fuels expected throughout the world, the increase in CO 2 emissions may prove to contribute even more significantly to global climate change. To address this problem, carbon sequestration scientists and engineers have proposed a number of methods to remove CO 2 from gas streams, such as chemical absorption with a solvent, membrane separation, and cryogenic fractionation. However, all of these methods are expensive and possibly cost-prohibitive for a specific application.

249

Atmospheric Carbon Dioxide Record from Mauna Loa  

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

SIO Air Sampling Network » Mauna Loa SIO Air Sampling Network » Mauna Loa Atmospheric Carbon Dioxide Record from Mauna Loa DOI: 10.3334/CDIAC/atg.035 graphics Graphics data Data Investigators R.F. Keeling, S.C. Piper, A.F. Bollenbacher and J.S. Walker Carbon Dioxide Research Group Scripps Institution of Oceanography University of California La Jolla, California 92093-0444, U.S.A. Period of Record 1958-2008 Methods Air samples at Mauna Loa are collected continuously from air intakes at the top of four 7-m towers and one 27-m tower. Four air samples are collected each hour for the purpose of determining the CO2 concentration. Determinations of CO2 are made by using a Siemens Ultramat 3 nondispersive infrared gas analyzer with a water vapor freeze trap. This analyzer registers the concentration of CO2 in a stream of air flowing at ~0.5

250

Coal Bed Sequestration of Carbon Dioxide  

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

COAL BED SEQUESTRATION OF CARBON DIOXIDE COAL BED SEQUESTRATION OF CARBON DIOXIDE R. Stanton (rstanton@usgs.gov; 703-648-6462) U.S. Geological Survey MS 956 National Center Reston, VA 20192 R. Flores (rflores@usgs.gov; 303-236-7774) U.S. Geological Survey MS 939, Denver Federal Center Denver, CO 80225 P.D. Warwick (pwarwick@usgs.gov; 703-648-6469) H. Gluskoter (halg@usgs.gov; 703-648-6429) U.S. Geological Survey MS 956 National Center Reston, VA 20192 G.D. Stricker (303-236-7763) U.S. Geological Survey MS 939, Denver Federal Center Denver, CO 80225 Introduction Geologic sequestration of CO 2 generated from fossil fuel combustion may be an environmentally attractive method to reduce the amount of greenhouse gas emissions. Of the geologic options, sequestering CO

251

Carbon Dioxide Emissions from Industrialized Countries  

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

6 6 Carbon Dioxide Emissions from Industrialized Countries Extended discussion here Carbon emissions per capita 1973 vs. 1991 by major end use. (Denmark comparison is 1972 and 1991) With the third Conference of the Parties (COP-3) in Kyoto approaching, there is a great deal of excitement over policies designed to reduce future carbon dioxide (CO2) emissions from fossil fuels. At COP-3, more than 130 nations will meet to create legally binding targets for CO2 reductions. Accordingly, we have analyzed the patterns of emissions arising from the end uses of energy (and electricity production) in ten industrialized countries, with surprising and, in some cases, worrisome results. The surprise is that emissions in many countries in the early 1990s were lower than in the 1970s in an absolute sense and on a per capita basis; the worry

252

Carbon dioxide utilization and seaweed production  

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

dioxide utilization and seaweed production dioxide utilization and seaweed production V.R.P.Sinha World Bank Project Bangladesh Fisheries Research Institute, Mymensingh, Bangladesh e-mails; vrpsinha@ mymensingh.net, vidyut_s@hotmail.com Lowell Fraley L.D. Fraley & Associates, LLC, P.O. Box 1525, Sugarland, TX 77487, USA, e-mail idf@hia.net BS Chowdhry ISS Consultants, Inc. 13111 Westheimer, Suite 303, Houston, Texas 77077, USA, e-mail bsc@issci.com Abstract: Stronger growth in many plants stimulated by increased CO 2 concentration should lead to greater biological productivity with an expected increase in the photosynthetic storage of carbon. Thus, the biosphere will serve as a sink for CO 2 , though it will also act as a source too, because of respiration. Normally net photosynthesis dominates in summer and

253

Solubilities of phenols in supercritical carbon dioxide  

SciTech Connect

Equilibrium solubilities of pure anthracene at 50 C, 1-naphthol at 35, 45, and 55 C, and hydroquinone at 35 and 45 C in supercritical carbon dioxide over a pressure range of about 85--300 bar have been measured using a supercritical fluid extractor coupled with an external high-pressure liquid chromatographer. The solubility results, along with those for other phenols reported in the literature, are correlated with the translated-modified Peng Robinson equation of state.

Coutsikos, P.; Magoulas, K.; Tassios, D. [National Technical Univ. of Athens (Greece)

1995-07-01T23:59:59.000Z

254

The production of pure hydrogen with simultaneous capture of carbon dioxide  

E-Print Network (OSTI)

dioxide is the combustion of carbona- ceous fuels. Currently, the combustion of oil, natural gas and coal accounts for 88 % of the world’s supply of primary energy, as seen in Table 1.1. While combustible renewables, such as wood, peat and animal waste... . For hydrogen, an environmentally-benign energy vector whose sole combustion product is water, to become a major energy source, it must be produced in an efficient, CO2- neutral manner. A process, which uses a packed bed of iron and its oxides, viz. Fe, Fe0.947O...

Bohn, Christopher

2010-10-12T23:59:59.000Z

255

Why Sequence Sulfur-Oxidizing Bacteria?  

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

Sulfur-Oxidizing Bacteria? Sulfur-Oxidizing Bacteria? Several environmental problems, such as acid rain, biocorrosion, etc., are caused by sulfur compounds, such as sulfur dioxide (SO2) and hydrogen sulfide (H2S). A sustainable process to remove these sulfur compounds is the production of elemental sulfur from H2S-containing gas streams by the use of sulfide-oxidizing bacteria. In this process, H2S is absorbed into the alkaline solution in the scrubber unit, followed by the biological oxidation of H2S to elemental sulfur and the recycling of water. With this two-step process, a variety of gas streams (i.e., natural gas, synthesis gas, biogas, and refinery gas) can be treated. For the treatment of sulfate-containing waste streams, an extra step has to be introduced: the transformation of sulfate into H2S by sulfate-reducing bacteria. In

256

Extracting metals directly from metal oxides  

DOE Patents (OSTI)

A method of extracting metals directly from metal oxides by exposing the oxide to a supercritical fluid solvent containing a chelating agent is described. Preferably, the metal is an actinide or a lanthanide. More preferably, the metal is uranium, thorium or plutonium. The chelating agent forms chelates that are soluble in the supercritical fluid, thereby allowing direct removal of the metal from the metal oxide. In preferred embodiments, the extraction solvent is supercritical carbon dioxide and the chelating agent is selected from the group consisting of .beta.-diketones, halogenated .beta.-diketones, phosphinic acids, halogenated phosphinic acids, carboxylic acids, halogenated carboxylic acids, and mixtures thereof. In especially preferred embodiments, at least one of the chelating agents is fluorinated. The method provides an environmentally benign process for removing metals from metal oxides without using acids or biologically harmful solvents. The chelate and supercritical fluid can be regenerated, and the metal recovered, to provide an economic, efficient process.

Wai, Chien M. (Moscow, ID); Smart, Neil G. (Moscow, ID); Phelps, Cindy (Moscow, ID)

1997-01-01T23:59:59.000Z

257

Extracting metals directly from metal oxides  

DOE Patents (OSTI)

A method of extracting metals directly from metal oxides by exposing the oxide to a supercritical fluid solvent containing a chelating agent is described. Preferably, the metal is an actinide or a lanthanide. More preferably, the metal is uranium, thorium or plutonium. The chelating agent forms chelates that are soluble in the supercritical fluid, thereby allowing direct removal of the metal from the metal oxide. In preferred embodiments, the extraction solvent is supercritical carbon dioxide and the chelating agent is selected from the group consisting of {beta}-diketones, halogenated {beta}-diketones, phosphinic acids, halogenated phosphinic acids, carboxylic acids, halogenated carboxylic acids, and mixtures thereof. In especially preferred embodiments, at least one of the chelating agents is fluorinated. The method provides an environmentally benign process for removing metals from metal oxides without using acids or biologically harmful solvents. The chelate and supercritical fluid can be regenerated, and the metal recovered, to provide an economic, efficient process. 4 figs.

Wai, C.M.; Smart, N.G.; Phelps, C.

1997-02-25T23:59:59.000Z

258

HYBRID HETEROGENEOUS CATALYSTS FOR HYDROGENATION OF CARBON DIOXIDE  

DOE Green Energy (OSTI)

HYBRID HETEROGENEOUS CATALYSTS FOR HYDROGENATION OF CARBON DIOXIDE Lucia M. Petkovic, Harry W. Rollins, Daniel M. Ginosar, and Kyle C. Burch Idaho National Laboratory P.O. Box 1625 Idaho Falls, ID 83415-2208 Introduction Anthropogenic emissions of carbon dioxide, a gas often associated with global warming, have increased considerably since the beginning of the industrial age.1 In the U.S., stationary CO2 sources, such as electricity generation plants, produce about one-third of the anthropogenic CO2 generation. Reports2 indicate that the power required to recover 90% of the CO2 from an integrated coal-fired power-plant is about 10% of the power-plant capacity. This energy requirement can be reduced to less than 1% if the recovered CO2 is applied to the production of synthetic fuels. However, the lack of efficient catalysts along with the costs of energy and hydrogen has prevented the development of technologies for direct hydrogenation of CO2.3 Although the cost of hydrogen for hydrogenating CO2 is not economically attractive at present, the future production of hydrogen by nuclear power sources could completely change this scenario.2 Still, an efficient catalyst will be essential for commercial application of those processes. The objective of the work presented here was the development of hybrid catalysts for one-step carbon dioxide hydrogenation to liquid fuels. The hybrid catalysts, which were prepared by two novel techniques, included a copper/zinc oxide catalytic function distributed within an acidic zeolitic matrix. Results of catalyst activity and selectivity studies at atmospheric pressure are presented in this contribution. Experimental Catalysts were prepared by two novel techniques and under several different conditions to produce copper/zinc oxide/zeolite materials. Once synthesized, samples were pelletized and the fraction between 40-60 mesh was utilized for the experiments. Two hundred milligrams of catalyst were loaded in a U-tube stainless steel reactor and a flow of 100 cm3/min of a 10:90 H2:Ar mixture was passed through the catalyst bed while the temperature was increased from room temperature to 513 K at 1.8 K/min and held at 513 K for 15 h. A reactant gas mixture composed by 10 cm3/min of CO2 and 30 cm3/min of H2 was then passed through the catalyst bed and the reaction products monitored by on-line gas chromatographic analyses using an SRI Multiple Gas Analyzer #2 equipped with 3 columns (MoleSieve 13X, Hayesep-D, and MXT-1) and 3 detectors (TCD, FID, and FID-methanizer). This GC system allowed for quantification of inert gases, CO, CO2, methanol, dimethylether, higher alcohols, water, and hydrocarbons up to C20. One hundred milligrams of a commercial syngas-to-methanol catalyst along with the same amount of a commercial zeolite catalyst was utilized under the same reaction conditions for comparison purposes. These catalysts were utilized either in two-layers (Com1) or mixed together (Com2). Results and Discussion Under the conditions applied in this study, the main reaction products were CO, CH3OH, CH3OCH3, and H2O. Methanol and dimethylether production rates and selectivities with respect to CO formation are presented in Figures 1 and 2, respectively. Although the activity of the synthesized catalysts did not surpass the commercial catalysts, the selectivity to oxygenates with respect to CO on most of the synthesized catalysts were better than on the commercial catalysts. For example, cat

Licia M. Petkovic; Harry W. Rollins; Daniel M. Ginosar; Kyle C. Burch

2006-09-01T23:59:59.000Z

259

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

260

EA-1336: Ocean Sequestration of Carbon Dioxide Field Experiment,  

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

336: Ocean Sequestration of Carbon Dioxide Field Experiment, 336: Ocean Sequestration of Carbon Dioxide Field Experiment, Pittsburgh, Pennsylvania EA-1336: Ocean Sequestration of Carbon Dioxide Field Experiment, Pittsburgh, Pennsylvania SUMMARY This EA evaluates the environmental impacts for the U.S. Department of Energy National Energy Technology Laboratory's proposal to participate with a group of international organizations in an experiment to evaluate the dispersion and diffusion of liquid carbon dioxide droplets in ocean waters. PUBLIC COMMENT OPPORTUNITIES None available at this time. DOCUMENTS AVAILABLE FOR DOWNLOAD May 4, 2001 EA-1336: Finding of No Significant Impact Ocean Sequestration of Carbon Dioxide Field Experiment May 4, 2001 EA-1336: Final Environmental Assessment Ocean Sequestration of Carbon Dioxide Field Experiment

Note: This page contains sample records for the topic "dioxide nitrous oxide" 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

Improving Repository Performance by Using DU Dioxide Fill  

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

DU Dioxide Fill DU Dioxide Fill Improving Repository Performance by Using DU Dioxide Fill Fills may improve repository performance by acting as sacrificial materials, which delay the degradation of SNF uranium dioxide. Because fill and SNF have the same chemical form of uranium (uranium dioxide), the DU dioxide in a repository is the only fill which has the same behavior as that of the SNF. In the natural environment, some uranium ore deposits have remained intact for very long periods of time. The outer parts of the ore deposit degrade while the inner parts of the deposit are protected. The same approach is proposed herein for protecting SNF. The application could use half or more of the DU inventory in the United States. Behavior of Uranium and Potential Behavior of a Waste Package with SNF and Fill

262

Building Technologies Office: Nano-Enabled Titanium Dioxide Ultraviolet  

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

Nano-Enabled Titanium Nano-Enabled Titanium Dioxide Ultraviolet Protective Layers for Cool-Color Roofing Research Project to someone by E-mail Share Building Technologies Office: Nano-Enabled Titanium Dioxide Ultraviolet Protective Layers for Cool-Color Roofing Research Project on Facebook Tweet about Building Technologies Office: Nano-Enabled Titanium Dioxide Ultraviolet Protective Layers for Cool-Color Roofing Research Project on Twitter Bookmark Building Technologies Office: Nano-Enabled Titanium Dioxide Ultraviolet Protective Layers for Cool-Color Roofing Research Project on Google Bookmark Building Technologies Office: Nano-Enabled Titanium Dioxide Ultraviolet Protective Layers for Cool-Color Roofing Research Project on Delicious Rank Building Technologies Office: Nano-Enabled Titanium Dioxide

263

Method of immobilizing carbon dioxide from gas streams  

DOE Patents (OSTI)

This invention is a method for rapidly and continuously immobilizing carbon dioxide contained in various industrial off-gas streams, the carbon dioxide being immobilized as dry, stable, and substantially water-insoluble particulates. Briefly, the method comprises passing the gas stream through a fixed or fluidized bed of hydrated barium hydroxide to remove and immobilize the carbon dioxide by converting the bed to barium carbonate. The method has several important advantages: it can be conducted effectively at ambient temperature; it provides a very rapid reaction rate over a wide range of carbon dioxide concentrations; it provides high decontamination factors; and it has a high capacity for carbon dioxide. The invention is especially well suited for the removal of radioactive carbon dioxide from off-gases generated by nuclear-fuel reprocessing facilities and nuclear power plants.

Holladay, David W. (Knoxville, TN); Haag, Gary L. (Oliver Springs, TN)

1979-01-01T23:59:59.000Z

264

National Level Co-Control Study of the Targets for Energy Intensity and Sulfur Dioxide in China  

E-Print Network (OSTI)

Ozawa Meida. 2001. “Carbon Dioxide Emissions from the Globalpost-combustion capture of carbon dioxide. ” InternationalIPCC Special Report on Carbon Dioxide Capture and Storage:

Zhou, Nan

2013-01-01T23:59:59.000Z

265

Model Documentation for the MiniCAM  

SciTech Connect

The MiniCAM, short for the Mini-Climate Assessment Model, is an integrated assessment model of moderate complexity focused on energy and agriculture sectors. The model produces emissions of greenhouse gases (carbon dioxide, methane and nitrous oxide) and other radiatively important substances such as sulfur dioxide. Through incorporation of the simple climate model MAGICC, the consequences of these emissions for climate change and sea-level rise can be examined. The MiniCAM is designed to be fast and flexible.

Brenkert, Antoinette L.; Smith, Steven J.; Kim, Son H.; Pitcher, Hugh M.

2003-07-17T23:59:59.000Z

266

Carbon Dioxide Capture by Absorption with Potassium Carbonate  

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

Carbon Dioxide Capture by Absorption Carbon Dioxide Capture by Absorption with Potassium Carbonate Background Although alkanolamine solvents, such as monoethanolamine (MEA), and solvent blends have been developed as commercially-viable options for the absorption of carbon dioxide (CO 2 ) from waste gases, natural gas, and hydrogen streams, further process improvements are required to cost-effectively capture CO 2 from power plant flue gas. The promotion of potassium carbonate (K

267

Selective Extraction of Uranium from Liquid or Supercritical Carbon Dioxide  

SciTech Connect

Current liquid-liquid extraction processes used in recycling irradiated nuclear fuel rely on (1) strong nitric acid to dissolve uranium oxide fuel, and (2) the use of aliphatic hydrocarbons as a diluent in formulating the solvent used to extract uranium. The nitric acid dissolution process is not selective. It dissolves virtually the entire fuel meat which complicates the uranium extraction process. In addition, a solvent washing process is used to remove TBP degradation products, which adds complexity to the recycling plant and increases the overall plant footprint and cost. A liquid or supercritical carbon dioxide (l/sc -CO2) system was designed to mitigate these problems. Indeed, TBP nitric acid complexes are highly soluble in l/sc -CO2 and are capable of extracting uranium directly from UO2, UO3 and U3O8 powders. This eliminates the need for total acid dissolution of the irradiated fuel. Furthermore, since CO2 is easily recycled by evaporation at room temperature and pressure, it eliminates the complex solvent washing process. In this report, we demonstrate: (1) A reprocessing scheme starting with the selective extraction of uranium from solid uranium oxides into a TBP-HNO3 loaded Sc-CO2 phase, (2) Back extraction of uranium into an aqueous phase, and (3) Conversion of recovered purified uranium into uranium oxide. The purified uranium product from step 3 can be disposed of as low level waste, or mixed with enriched uranium for use in a reactor for another fuel cycle. After an introduction on the concept and properties of supercritical fluids, we first report the characterization of the different oxides used for this project. Our extraction system and our online monitoring capability using UV-Vis absorbance spectroscopy directly in sc-CO2 is then presented. Next, the uranium extraction efficiencies and kinetics is demonstrated for different oxides and under different physical and chemical conditions: l/sc -CO2 pressure and temperature, TBP/HNO3 complex used, reductant or complexant used for selectivity, and ionic liquids used as supportive media. To complete the extraction and recovery cycle, we then demonstrate uranium back extraction from the TBP loaded sc-CO2 phase into an aqueous phase and the characterization of the uranium complex formed at the end of this process. Another aspect of this project was to limit proliferation risks by either co-extracting uranium and plutonium, or by leaving plutonium behind by selectively extracting uranium. We report that the former is easily achieved, since plutonium is in the tetravalent or hexavalent oxidation state in the oxidizing environment created by the TBP-nitric acid complex, and is therefore co-extracted. The latter is more challenging, as a reductant or complexant to plutonium has to be used to selectively extract uranium. After undertaking experiments on different reducing or complexing systems (e.g., AcetoHydroxamic Acid (AHA), Fe(II), ascorbic acid), oxalic acid was chosen as it can complex tetravalent actinides (Pu, Np, Th) in the aqueous phase while allowing the extraction of hexavalent uranium in the sc-CO2 phase. Finally, we show results using an alternative media to commonly used aqueous phases: ionic liquids. We show the dissolution of uranium in ionic liquids and its extraction using sc-CO2 with and without the presence of AHA. The possible separation of trivalent actinides from uranium is also demonstrated in ionic liquids using neodymium as a surrogate and diglycolamides as the extractant.

Farawila, Anne F.; O'Hara, Matthew J.; Wai, Chien M.; Taylor, Harry Z.; Liao, Yu-Jung

2012-07-31T23:59:59.000Z

268

Organoclay Sorbent for Removal of Carbon Dioxide from Gas ...  

Organoclay Sorbent for Removal of Carbon Dioxide from Gas ... required for sequestration, an area of research identified as a high priority

269

EA-1846: Demonstration of Carbon Dioxide Capture and Sequestration...  

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

46: Demonstration of Carbon Dioxide Capture and Sequestration of Steam Methane Reforming Process Gas Used for Large-Scale Hydrogen Production, Port Arthur, Texas EA-1846:...

270

Carbon Dioxide, Hydrographic, and Chemical Data Obtained During...  

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

Marine Environmental Laboratory National Oceanic and Atmospheric Administration Seattle, Washington, U.S.A. Prepared by Alexander Kozyr1 Carbon Dioxide Information Analysis...

271

Synchrotron X-ray Studies of Supercritical Carbon Dioxide/ Reservoir...  

Open Energy Info (EERE)

Edit with form History Facebook icon Twitter icon Synchrotron X-ray Studies of Supercritical Carbon Dioxide Reservoir Rock Interfaces Geothermal Lab Call Project Jump to:...

272

Average prices for spot sulfur dioxide emissions allowances at ...  

U.S. Energy Information Administration (EIA)

The weighted average spot price for sulfur dioxide (SO 2) emissions allowances awarded to winning bidders at Environmental Protection Agency's (EPA) annual auction on ...

273

The Structure of Uranium Dioxide Grain Boundaries and its ...  

Science Conference Proceedings (OSTI)

The atomic structures of symmetric ?5 tilt, ?5 twist, and amorphous grain boundaries in uranium dioxide are explored in this work using empirical potentials and ...

274

Development of Geologic Storage Estimates for Carbon Dioxide  

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

Storage Estimates for Carbon Dioxide Prepared for U.S. Department of Energy National Energy Technology Laboratory Carbon Storage Program September 2010 Summary of the...

275

Polyaniline-Based Membranes for Separating Carbon Dioxide and Methane  

Berkeley Lab researchers have optimized polymer membrane technology to more efficiently remove carbon dioxide (CO2) from natural gas. The invention ...

276

Bulk separation of carbon dioxide from natural gas  

SciTech Connect

In the bulk separation of carbon dioxide from feedstocks containing same in admixture with relatively nonsorbable gases using a zeolitic molecular sieve to adsorb selectively the carbon dioxide, higher product purity is attained by terminating the adsorption stroke using the feedstock while the bed still has capacity to adsorb more carbon dioxide at the same conditions, then purging the void space hydrocarbons from the bed using product carbon dioxide at a high partial pressure, and finally desorbing the bed by pressure reduction. (3 claims)

Collins, J.J.

1973-08-14T23:59:59.000Z

277

Historical Carbon Dioxide Record from the Vostok Ice Core  

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

Vostok Ice Core Historical Carbon Dioxide Record from the Vostok Ice Core graphics Graphics data Data Investigators J.-M. Barnola, D. Raynaud, C. Lorius Laboratoire de Glaciologie...

278

Historical Carbon Dioxide Record from the Siple Station Ice Core  

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

Siple Station Ice Core Historical Carbon Dioxide Record from the Siple Station Ice Core graphics Graphics data Data Investigators A. Neftel, H. Friedli, E. Moor, H. Ltscher, H....

279

Segregation of Ru to Edge Dislocations in Uranium Dioxide  

Science Conference Proceedings (OSTI)

Presentation Title, Segregation of Ru to Edge Dislocations in Uranium Dioxide. Author(s), Anuj Goyal, Bowen Deng, Minki Hong, Aleksandr Chernatynskiy, ...

280

Carbon Ion Pump for Carbon Dioxide Removal - Energy Innovation ...  

coal fired power plants; oil or gas fired power plants; cement production; bio-fuel combustion; Separation of carbon dioxide from other combustion ...

Note: This page contains sample records for the topic "dioxide nitrous oxide" 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

Geomechanical risks in coal bed carbon dioxide sequestration  

E-Print Network (OSTI)

SAF. 1958. The strength of coal in triaxial compression.Geomechanical Risks in Coal Bed Carbon Dioxide Sequestrationof leakage of CO 2 from coal bed sequestration projects. The

Myer, Larry R.

2003-01-01T23:59:59.000Z

282

Figure 18. Energy-related carbon dioxide emissions in three ...  

U.S. Energy Information Administration (EIA)

Sheet3 Sheet2 Sheet1 Figure 18. Energy-related carbon dioxide emissions in three cases, 2005-2040 (million metric tons) Extended Policies No Sunset

283

Carbon Dioxide, Hydrographic, and Chemical Data Obtained in the...  

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

Oceanographic Institution Woods Hole, Massachusetts, U.S.A. Prepared by Alexander Kozyr Carbon Dioxide Information Analysis Center Oak Ridge National Laboratory Oak Ridge,...

284

Dissociation of carbon dioxide in atmospheric pressure microchannel plasma devices.  

E-Print Network (OSTI)

??Plasma discharge of carbon dioxide at atmospheric pressure was successfully demonstrated in microchannel plasma devices at breakdown voltages lower than 1 kVRMS. Optical emissions of… (more)

Oh, Taegon

2013-01-01T23:59:59.000Z

285

Carbon Dioxide, Hydrographic, and Chemical Data Obtained During...  

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

Hole Oceanographic Institution Woods Hole, Massachusetts Prepared by Alexander Kozyr Carbon Dioxide Information Analysis Center Oak Ridge National Laboratory Oak Ridge,...

286

Benchmark Results for TraPPE Carbon Dioxide  

Science Conference Proceedings (OSTI)

Benchmark results for TraPPE Carbon Dioxide. The purpose of these pages is to provide some explicit results from Monte ...

2013-09-20T23:59:59.000Z

287

Carbon Dioxide, Hydrographic, and Chemical Data Obtained During...  

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

**Scripps Institution of Oceanography La Jolla, California Prepared by Alexander Kozyr*** Carbon Dioxide Information Analysis Center Oak Ridge National Laboratory Oak Ridge,...

288

Available Technologies: Carbon Dioxide Capture at a Reduced Cost  

Scientists at Berkeley Lab have developed a method that reduces the expense of capturing carbon dioxide generated by the combustion of fossil fuels. This technology ...

289

Carbon Dioxide Capture at a Reduced Cost - Energy Innovation ...  

Scientists at Berkeley Lab have developed a method that reduces the expense of capturing carbon dioxide generated by the combustion of fossil fuels. This technology ...

290

Amine Enriched Solid Sorbents for Carbon Dioxide Capture Opportunity  

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

Laboratory is seeking licensing partners interested in implementing United States Patent Number 6,547,854 entitled "Amine Enriched Solid Sorbents for Carbon Dioxide Capture."...

291

EPA's Proposed Greenhouse Gas Reporting Rule for Carbon Dioxide...  

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

EPA's Proposed Greenhouse Gas Reporting Rule for Carbon Dioxide Injection and Geologic Sequestration Mark de Figueiredo U.S. Environmental Protection Agency RCSP Annual Review...

292

Atmospheric Carbon Dioxide Record from Flask Measurements at...  

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

Island Atmospheric Carbon Dioxide Record from Flask Measurements at Lampedusa Island graphics Graphics data Data Investigators Paolo Chamard, Luigi Ciattaglia, Alcide di Sarra,...

293

Louisiana Geologic Sequestration of Carbon Dioxide Act (Louisiana...  

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

industrial, or other uses, including the use of carbon dioxide for enhanced recovery of oil and gas. The mandates a coordinated statewide program related to the storage...

294

Carbon ion pump for removal of carbon dioxide from combustion ...  

Biomass and Biofuels; Building Energy Efficiency; ... Carbon ion pump for removal of carbon dioxide from combustion gas and other gas mixtures United States Patent ...

295

The carbon footprint analysis of wastewater treatment plants and nitrous oxide emissions from full-scale biological nitrogen removal processes in Spain  

E-Print Network (OSTI)

This thesis presents a general model for the carbon footprint analysis of advanced wastewater treatment plants (WWTPs) with biological nitrogen removal processes, using a life cycle assessment (LCA) approach. Literature ...

Xu, Xin, S.M. Massachusetts Institute of Technology

2013-01-01T23:59:59.000Z

296

Carbon Dioxide Sequestration Industrial-scale processes are available for separating carbon dioxide from the post-  

E-Print Network (OSTI)

-intensive and would lower the thermal efficiency of coal gasification power plants. Selective separation membrane from the post- combustion flue gas of a steam-electric power plant or from the synthesis gas fuel of a coal gasification power plant. The separated carbon dioxide can be compressed and transported

297

Method for Extracting and Sequestering Carbon Dioxide  

DOE Patents (OSTI)

A method and apparatus to extract and sequester carbon dioxide (CO2) from a stream or volume of gas wherein said method and apparatus hydrates CO2, and reacts the resulting carbonic acid with carbonate. Suitable carbonates include, but are not limited to, carbonates of alkali metals and alkaline earth metals, preferably carbonates of calcium and magnesium. Waste products are metal cations and bicarbonate in solution or dehydrated metal salts, which when disposed of in a large body of water provide an effective way of sequestering CO2 from a gaseous environment.

Rau, Gregory H.; Caldeira, Kenneth G.

2005-05-10T23:59:59.000Z

298

Method For Selective Catalytic Reduction Of Nitrogen Oxides  

DOE Patents (OSTI)

A method for catalytically reducing nitrogen oxide compounds (NO.sub.x, defined as nitric oxide, NO, +nitrogen dioxide, NO.sub.2) in a gas by a material comprising a base metal consisting essentially of CuO and Mn, and oxides of Mn, on an activated metal hydrous metal oxide support, such as HMO:Si. A promoter, such as tungsten oxide or molybdenum oxide, can be added and has been shown to increase conversion efficiency. This method provides good conversion of NO.sub.x to N.sub.2, good selectivity, good durability, resistance to SO.sub.2 aging and low toxicity compared with methods utilizing vanadia-based catalysts.

Mowery-Evans, Deborah L. (Broomfield, CO); Gardner, Timothy J. (Albuquerque, NM); McLaughlin, Linda I. (Albuquerque, NM)

2005-02-15T23:59:59.000Z

299

Method for selective catalytic reduction of nitrogen oxides  

DOE Patents (OSTI)

A method for catalytically reducing nitrogen oxide compounds (NO.sub.x, defined as nitric oxide, NO, +nitrogen dioxide, NO.sub.2) in a gas by a material comprising a base metal consisting essentially of CuO and Mn, and oxides of Mn, on an activated metal hydrous metal oxide support, such as HMO:Si. A promoter, such as tungsten oxide or molybdenum oxide, can be added and has been shown to increase conversion efficiency. This method provides good conversion of NO.sub.x to N.sub.2, good selectivity, good durability, resistance to SO.sub.2 aging and low toxicity compared with methods utilizing vanadia-based catalysts.

Mowery-Evans, Deborah L. (Broomfield, CO); Gardner, Timothy J. (Albuquerque, NM); McLaughlin, Linda I. (Albuquerque, NM)

2005-02-15T23:59:59.000Z

300

China's Industrial Carbon Dioxide Emissions in Manufacturing Subsectors and in Selected Provinces  

E-Print Network (OSTI)

U.S. Energy-Related Carbon Dioxide Emissions, 2010. ” AugustChina’s Industrial Carbon Dioxide Emissions in ManufacturingChina’s Industrial Carbon Dioxide Emissions in Manufacturing

Lu, Hongyou

2013-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "dioxide nitrous oxide" 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

Structural and electronic studies of complexes relevant to the electrocatalyic reduction of carbon dioxide  

E-Print Network (OSTI)

1981) Facile reduction of carbon dioxide by anionic Group 6bReduction of Carbon Dioxide on Mercury Electrode.in Reduction of Carbon-Dioxide. J. Chem. Soc. -Chem.

Benson, Eric Edward

2012-01-01T23:59:59.000Z

302

Pressure buildup during supercritical carbon dioxide injection from a partially penetrating borehole into gas reservoirs  

E-Print Network (OSTI)

interface solution for carbon dioxide injection into porousJ.E. Fluid Dynamics of Carbon Dioxide Disposal into SalineGeologic storage of carbon dioxide as a climate change

Mukhopadhyay, S.

2013-01-01T23:59:59.000Z

303

Application of gaseous disinfectants ozone and chlorine dioxide for inactivation of Bacillus subtilis spores  

E-Print Network (OSTI)

An assessment of ozone and chlorine dioxide for treatment ofAston, R. ; Synan, J. , “Chlorine dioxide as a bactericide62, 80. 14. Keane, T. , “ Chlorine dioxide – why all the

Aydogan, Ahmet

2006-01-01T23:59:59.000Z

304

Lessons Learned from Natural and Industrial Analogues for Storage of Carbon Dioxide in Deep Geological Formations  

E-Print Network (OSTI)

and E.R. Slatick, Carbon Dioxide Emission Factors for Coal,oxygen-deficiency is a factor. CARBON DIOXIDE - CO 2 MSDS (Carbon Dioxide will be reached before oxygen-deficiency is a factor.

Benson, Sally M.; Hepple, Robert; Apps, John; Tsang, Chin-Fu; Lippmann, Marcelo

2002-01-01T23:59:59.000Z

305

EIA - International Energy Outlook 2009-Energy-Related Carbon Dioxide  

Gasoline and Diesel Fuel Update (EIA)

Energy-Related Carbon Dioxide Emissions Energy-Related Carbon Dioxide Emissions International Energy Outlook 2009 Chapter 8 - Energy-Related Carbon Dioxide Emissions In 2006, non-OECD energy-related emissions of carbon dioxide exceeded OECD emissions by 14 percent. In 2030, energy-related carbon dioxide emissions from the non-OECD countries are projected to exceed those from the OECD countries by 77 percent. Figure 80. World Energy-Related Carbon Dioxide Emissions, 2006-2030 (Billion Metric Tons). Need help, contact the National Energy Information Center at 202-586-8800. Figure Data Figure 81. World Energy-Related Carbon Dioxide Emissions by Fuel Type, 1990-2030 (Billion Metric Tons). Need help, contact the National Energy Information Center at 202-586-8800. Figure Data Figure 82. U.S. Energy-Related Carbon Dioxide Emissions by Fuel in IEO2008 and IEO2009, 2006, 2015, and 2030 (billion metric tons). Need help, contact the National Energy Information Center at 202-586-8800.

306

Carbon Dioxide Sequestration with Flue Gas Desulfurization (FGD) Gypsum  

Science Conference Proceedings (OSTI)

Carbonation of industrial alkaline residues can be used as a CO2 sequestration technology to reduce carbon dioxide emissions. In this study, alkaline Ca-rich flue gas desulfurization (FGD) gypsum samples were carbonated to a varying extent. These materials ... Keywords: FGD gypsum, carbonation, carbon dioxide

Hongqi Wang; Ningning Sun; Rona J. Donahoe

2009-07-01T23:59:59.000Z

307

Analysis of data for the carbon dioxide capture domain  

Science Conference Proceedings (OSTI)

To tackle the global concern for adverse impact of greenhouse gas (GHG) emissions, the post combustion carbon dioxide (CO"2) capture technology is commonly adopted for reducing industrial CO"2 emissions, for example, from power generation plants. The ... Keywords: Carbon dioxide capture, Data modeling, Expert validation, Neural networks, Sensitivity analysis

Yuxiang Wu; Christine W. Chan

2011-02-01T23:59:59.000Z

308

A monitoring and diagnostic expert system for carbon dioxide capture  

Science Conference Proceedings (OSTI)

The research objective is to design and construct a knowledge-based decision support system for monitoring, control and diagnosis of the carbon dioxide capture process, which is a complicated task involving manipulation of sixteen components and their ... Keywords: Carbon dioxide capture, Diagnosis, Knowledge-based decision support system, Monitoring

Q. Zhou; C. W. Chan; P. Tontiwachiwuthikul

2009-03-01T23:59:59.000Z

309

Carbon dioxide emission during forest fires ignited by lightning  

E-Print Network (OSTI)

In this paper we developed the model for the carbon dioxide emission from forest fire. The master equation for the spreading of the carbon dioxide to atmosphere is the hyperbolic diffusion equation. In the paper we study forest fire ignited by lightning. In that case the fores fire has the well defined front which propagates with finite velocity.

Magdalena Pelc; Radoslaw Osuch

2009-03-31T23:59:59.000Z

310

Historical Sulfur Dioxide Emissions 1850-2000: Methods and Results  

E-Print Network (OSTI)

PNNL-14537 Historical Sulfur Dioxide Emissions 1850-2000: Methods and Results S.J. Smith E;PNNL-14537 Historical Sulfur Dioxide Emissions 1850-2000: Methods and Results PNNL Research Report Joint Global Change Research Institute 8400 Baltimore Avenue College Park, Maryland 20740 #12;PNNL-14537

Hultman, Nathan E.

311

Reduction of carbon dioxide emissions by mineral carbonation  

Science Conference Proceedings (OSTI)

The study investigates the technologies that have the potential to provide feasible reduction of carbon dioxide (CO2) from a reference power plant. Particular focus has been given to mineral carbonation (at 1 bar) in which magnesium (Mg) and/or ... Keywords: carbon dioxide, emissions, mineral carbonation

C. J. Sturgeon; M. G. Rasul; Ashfaque Ahmed Chowdhury

2010-02-01T23:59:59.000Z

312

Pages that link to "Cost and Performance of Carbon Dioxide Capture...  

Open Energy Info (EERE)

icon Pages that link to "Cost and Performance of Carbon Dioxide Capture from Power Generation" Cost and Performance of Carbon Dioxide Capture from Power Generation...

313

Mechanistic Modeling of an Underbalanced Drilling Operation Utilizing Supercritical Carbon Dioxide.  

E-Print Network (OSTI)

??Mechanistic modeling of an underbalanced drilling operation using carbon dioxide has been developed in this research. The use of carbon dioxide in an underbalanced drilling… (more)

ALAdwani, Faisal Abdullah

2007-01-01T23:59:59.000Z

314

Carbon Dioxide Heat Pump Water Heater Research Project | Department of  

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

Emerging Technologies » Carbon Dioxide Heat Pump Water Heater Emerging Technologies » Carbon Dioxide Heat Pump Water Heater Research Project Carbon Dioxide Heat Pump Water Heater Research Project The U.S. Department of Energy is currently conducting research into carbon dioxide (CO2) heat pump water heaters. This project will employ innovative techniques to adapt water heating technology to meet U.S. market requirements, including specifications, cost, and performance targets. Carbon dioxide is a refrigerant with a global warming potential (GWP) of 1. The CO2 heat pump water heater research seeks to develop an improved life cycle climate performance compared to conventional refrigerants. For example, R134a, another type of refrigerant, has a GWP of 1,300. Project Description This project seeks to develop a CO2-based heat pump water heater (HPWH)

315

Microbial Sequestration of Carbon Dioxide and Subsequent Conversion to Methane  

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

Sequestration of Carbon Dioxide and Subsequent Sequestration of Carbon Dioxide and Subsequent conversion to Methane By Nirupam Pal Associate Professor California Polytechnic State University San Luis Obispo, CA 93401 Email : npal@calpoly.edu Phone : (805) 756-1355 INTRODUCTION The rising level of carbon dioxide in the atmosphere has been of growing concern in recent years. The increasing levels of carbon dioxide, the most dominant component of greenhouse gases, contribute to global warming and changing global weather patterns which could potentially lead to catastrophic events that could threaten life in every form on this planet. The level of carbon dioxide in the worlds atmosphere has increased from about 280 ppm in 1850 to the current level of approximately 350 ppm. There are several natural sources and sinks of

316

DOE Report Assesses Potential for Carbon Dioxide Storage Beneath Federal  

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

Report Assesses Potential for Carbon Dioxide Storage Beneath Report Assesses Potential for Carbon Dioxide Storage Beneath Federal Lands DOE Report Assesses Potential for Carbon Dioxide Storage Beneath Federal Lands May 14, 2009 - 1:00pm Addthis Washington, DC - As a complementary document to the U.S. Department of Energy's Carbon Sequestration Atlas of the United States and Canada issued in November 2008, the Office of Fossil Energy's National Energy Technology Laboratory has now released a report that provides an initial estimate of the potential to store carbon dioxide (CO2) underneath millions of acres of Federal lands. The report, Storage of Captured Carbon Dioxide Beneath Federal Lands, estimates and characterizes the storage potential that lies beneath some of the more than 400 million acres of Federal land available for lease.

317

Innovative Concepts for Beneficial Reuse of Carbon Dioxide | Department of  

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

Innovative Concepts for Beneficial Reuse of Carbon Dioxide Innovative Concepts for Beneficial Reuse of Carbon Dioxide Innovative Concepts for Beneficial Reuse of Carbon Dioxide Funding for 12 projects to test innovative concepts for the beneficial use of carbon dioxide (CO2) was announced by the U.S. Department of Energy. The awards are part of $1.4 billion in funding from the American Recovery and Reinvestment Act (ARRA) for projects that will capture carbon dioxide from industrial sources. These 12 projects will engage in a first phase feasibility study that will examine beneficial uses in a variety of ways, including mineralization to carbonates directly through conversion of CO2 in flue gas; the use of CO2 from power plants or industrial applications to grow algae/biomass; and conversion of CO2 to fuels and chemicals. Each project will be subject to

318

Haverford Researchers Create Carbon Dioxide-Separating Polymer  

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

Haverford College Haverford College Researchers Create Carbon Dioxide-Separating Polymer Haverford College Researchers Create Carbon Dioxide-Separating Polymer August 1, 2012 | Tags: Basic Energy Sciences (BES), Chemistry, Hopper Rebecca Raber, rraber@haverford.edu, +1 610 896 1038 gtoc.jpg Carbon dioxide gas separation is important for many environmental and energy applications. Molecular dynamics simulations are used to characterize a two-dimensional hydrocarbon polymer, PG-ES1, that uses a combination of surface adsorption and narrow pores to separate carbon dioxide from nitrogen, oxygen, and methane gases. Image by Joshua Schrier, Haverford College. Carbon dioxide is the primary greenhouse gas emitted through human activities, such as the combustion of fossil fuels for energy and

319

Carbon dioxide absorbent and method of using the same  

DOE Patents (OSTI)

In accordance with one aspect, the present invention provides an amino-siloxane composition comprising at least one of structures I, II, III, IV or V said compositions being useful for the capture of carbon dioxide from gas streams such as power plant flue gases. In addition, the present invention provides methods of preparing the amino-siloxane compositions are provided. Also provided are methods for reducing the amount of carbon dioxide in a process stream employing the amino-siloxane compositions of the invention as species which react with carbon dioxide to form an adduct with carbon dioxide. The reaction of the amino-siloxane compositions provided by the present invention with carbon dioxide is reversible and thus, the method provides for multicycle use of said compositions.

Perry, Robert James (Niskayuna, NY); Lewis, Larry Neil (Scotia, NY); O' Brien, Michael Joseph (Clifton Park, NY); Soloveichik, Grigorii Lev (Latham, NY); Kniajanski, Sergei (Clifton Park, NY); Lam, Tunchiao Hubert (Clifton Park, NY); Lee, Julia Lam (Niskayuna, NY); Rubinsztajn, Malgorzata Iwona (Ballston Spa, NY)

2011-10-04T23:59:59.000Z

320

Method for fluorination of uranium oxide  

SciTech Connect

Highly pure uranium hexafluoride is made from uranium oxide and fluorine. The uranium oxide, which includes UO.sub.3, UO.sub.2, U.sub.3 O.sub.8 and mixtures thereof, is introduced together with a small amount of a fluorine-reactive substance, selected from alkali chlorides, silicon dioxide, silicic acid, ferric oxide, and bromine, into a constant volume reaction zone. Sufficient fluorine is charged into the zone at a temperature below approximately 0.degree. C. to provide an initial pressure of at least approximately 600 lbs/sq. in. at the ambient atmospheric temperature. The temperature is then allowed to rise in the reaction zone until reaction occurs.

Petit, George S. (Oak Ridge, TN)

1987-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "dioxide nitrous oxide" 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

Generation and Solid Oxide Fuel Cell Carbon Sequestration in Northwest Indiana  

DOE Green Energy (OSTI)

The objective of the project is to develop the technology capable of capturing all carbon monoxide and carbon dioxide from natural gas fueled Solid Oxide Fuel Cell (SOFC) system. In addition, the technology to electrochemically oxidize any remaining carbon monoxide to carbon dioxide will be developed. Success of this R&D program would allow for the generation of electrical power and thermal power from a fossil fuel driven SOFC system without the carbon emissions resulting from any other fossil fueled power generationg system.

Kevin Peavey; Norm Bessette

2007-09-30T23:59:59.000Z

322

Fuel electrode containing pre-sintered nickel/zirconia for a solid oxide fuel cell  

DOE Patents (OSTI)

A fuel cell structure (2) is provided, having a pre-sintered nickel-zirconia fuel electrode (6) and an air electrode (4), with a ceramic electrolyte (5) disposed between the electrodes, where the pre-sintered fuel electrode (6) contains particles selected from the group consisting of nickel oxide, cobalt and cerium dioxide particles and mixtures thereof, and titanium dioxide particles, within a matrix of yttria-stabilized zirconia and spaced-apart filamentary nickel strings having a chain structure, and where the fuel electrode can be sintered to provide an active solid oxide fuel cell.

Ruka, Roswell J. (Pittsburgh, PA); Vora, Shailesh D. (Monroeville, PA)

2001-01-01T23:59:59.000Z

323

Implications of mercury interactions with band-gap semiconductor oxides  

SciTech Connect

Titanium dioxide is a well-known photooxidation catalyst. It will oxidize mercury in the presence of ultraviolet light from the sun and oxygen and/or moisture to form mercuric oxide. Several companies manufacture self-cleaning windows. These windows have a transparent coating of titanium dioxide. The titanium dioxide is capable of destroying organic contaminants in air in the presence of ultraviolet light from the sun, thereby keeping the windows clean. The commercially available self-cleaning windows were used to sequester mercury from oxygen–nitrogen mixtures. Samples of the self-cleaning glass were placed into specially designed photo-reactors in order to study the removal of elemental mercury from oxygen–nitrogen mixtures resembling air. The possibility of removing mercury from ambient air with a self-cleaning glass apparatus is examined. The intensity of 365-nm ultraviolet light was similar to the natural intensity from sunlight in the Pittsburgh region. Passive removal of mercury from the air may represent an option in lieu of, or in addition to, point source clean-up at combustion facilities. There are several common band-gap semiconductor oxide photocatalysts. Sunlight (both the ultraviolet and visible light components) and band-gap semiconductor particles may have a small impact on the global cycle of mercury in the environment. The potential environmental consequences of mercury interactions with band-gap semiconductor oxides are discussed. Heterogeneous photooxidation might impact the global transport of elemental mercury emanating from flue gases.

Granite, E.J.; King, W.P.; Stanko, D.C.; Pennline, H.W.

2008-09-01T23:59:59.000Z

324

Microbial and objective quality of whole muscle beef cuts packaged in film containing chlorine dioxide  

E-Print Network (OSTI)

The microbial and objective quality of top round steak treated with two deferent prototype chlorine dioxide containing films were evaluated deleing 14 days of refrigerated storage. The films were designed to deliver different dose rates of chlorine dioxide when in contact with tissue. A high dose rate film in combination with dip treatments resulted in a 1.0 log?? reduction of total hemophilic aerobes, total coliforms, and total lactic acid bacteria. However, this same film caused undesirable characteristics including the rapid loss of the red color associated with fresh beef and the development of a green colored pigment. This color change corresponded to a decrease in Hunter a* values. Ascorbic acid treatments slightly inhibited the development of green color after 2 days of storage, but the protective effect was not evident after 6 days of storage and the color remained undesirable. Chlorine dioxide released from the high dose rate film penetrated immediately into the surface of the beef to a depth of 1mm into the surface of the beef after 6 days of storage, and did not penetrate more than 2mm deep after 14 days of storage. The concentration of myoglobin in extracts of the treated samples decreased sharply after 2 days storage, suggesting oxidative degradation and possibly the formation of a compound similar to the green pigment cholemyoglobin. The TBA values of beef treated with the high dose rate film increased during storage but remained blow 1.0. A low chlorine dioxide dose rate film did not produce any microbiological or objective changes in the beef. The dose rate for the high dose rate film was 32ppm/h, as determined by neutron activation analysis. It decreased rapidly to 0ppm/h after 10 days storage and was not constant during the test period. Based on the unacceptable attributes produced by the high dose rate film, it may be better suited for low fat cuts of pork, ash, or chicken that are less susceptible to color changes and quality losses associated with undesirable oxidative changes.

Knight, Timothy David

1999-01-01T23:59:59.000Z

325

Selected genomic and phenotypic responses of Salmonella serovars to chlorine, chlorine dioxide, and cetylpyridinium chloride  

E-Print Network (OSTI)

Non-typhoidal Salmonella enterica serovars continue to be the leading cause of foodborne illnesses in United States. Chlorine, chlorine related, and quaternary compounds are generally used for disinfecting carcasses and equipment in processing industries. The current study was aimed at understanding the inactivation kinetics of four Salmonella serovars to chlorine, chlorine dioxide and cetylpyridinium chloride (CPC). The transcriptomic responses to oxidative stress was investigated in stationary and log phase cells of S. Typhimurium. The study was also aimed at understanding the effect of the chemicals on the expression of virulence genes associated with the Salmonella Pathogenecity Island 1 (SPI1). The possible induction of the viable but nonculturable (VBNC) state in Salmonella due to CPC was also investigated. The inactivation parameters for each serovar and the chemical were estimated based on the Hom's model, ln (N/N0) = -k C^n T^m and it appeared that while disinfectant contact time was significant, biocide concentration in the overall disinfection was insignificant. This was true especially for chlorine and CPC with subtle differences observed between the serovars. The inactivation efficacy was, however, dependent on both concentration and the exposure time for chlorine dioxide. The highest degree of inactivation was obtained with chlorine followed by chlorine dioxide and CPC. Transcriptomic responses of S. Typhimurium revealed significant downregulation of several metabolic processes such as tricarboxylic acid cycle, oxidative phosphorylation, and amino acid biosynthesis in both log and stationary phase cells. Several stress related genes such as usp, rpoS and ompR were upregulated in the stationary phase cells. Majority of the virulence genes associated with the SPI1 were found to be downregulated for all the treatments. While treatment with chlorine and CPC caused downregulation of all the virulence genes, treatment with chlorine dioxide caused significant upregulation of few (hilC, invC, sipA and sipB) genes associated with the SPI1. Finally, the induction of VBNC state was not concluded as a result of treatment with CPC. However, significant percentage of cells (45 percent) with intact membrane was established based on the BacLight assayTM.

Kakani, Grihalakshmi

2011-05-01T23:59:59.000Z

326

DEVELOPMENT AND MECHANISTIC STUDIES OF THE CHROMIUM TETRAMETHYLTETRAAZAANNULENE CATALYST SYSTEM FOR THE COPOLYMERIZATION OF CARBON DIOXIDE AND EPOXIDES  

E-Print Network (OSTI)

A prominent goal of scientists is to develop products and processes to meet the ever-growing needs of society. Today's needs include products that are economical, specialized, and made through processes with minimal impact on the environment. One such product that serves an important and widespread need is poly(bisphenol A carbonate) for its physical properties and ease of synthesis and processing. However, this polymer does not meet the growing need of being environmentally benign as production involves carcinogenic, chlorinated solvents and toxic monomers that can leach out from the polymer product. An answer to this new demand is the development of a different process for the production of polycarbonate plastics utilizing carbon dioxide and epoxides. Carbon dioxide is an attractive monomer that is cheap and nontoxic, and its utilization signifies an important contribution to counteract global greenhouse emissions. The stability of carbon dioxide has posed a significant and complex challenge towards its utilization. Epoxides are attractive since they are synthesized from a wide variety of olefins, both naturally occurring and those derived from petroleum. The exploration of catalysts to facilitate the coupling of epoxides to carbon dioxide to afford polycarbonates has been under investigation in the Darensbourg lab for fifteen years, and has lead to the development of several successful systems such as zinc bisphenoxides and chromium salens. This dissertation focuses on the development of another successful catalyst system, chromium tetramethyltetraazaannulene, and further elucidation of the mechanism by which polycarbonates are formed. Herein, aspects of the copolymerization process using this system will be discussed in detail, such as cocatalyst and pressure dependence, catalyst derivatization, and kinetic and mechanistic investigations. The end result of these investigations is the development of the most active chromium-based catalyst for the copolymerization of cyclohexene oxide and carbon dioxide and a better understanding of how the copolymer product is produced.

Fitch, Shawn

2009-05-01T23:59:59.000Z

327

Carbon Dioxide Sequestration in Geologic Coal Formations  

SciTech Connect

BP Corporation North America, Inc. (BP) currently operates a nitrogen enhanced recovery project for coal bed methane at the Tiffany Field in the San Juan Basin, Colorado. The project is the largest and most significant of its kind wherein gas is injected into a coal seam to recover methane by competitive adsorption and stripping. The Idaho National Engineering and Environmental Laboratory (INEEL) and BP both recognize that this process also holds significant promise for the sequestration of carbon dioxide, a greenhouse gas, while economically enhancing the recovery of methane from coal. BP proposes to conduct a CO2 injection pilot at the tiffany Field to assess CO2 sequestration potential in coal. For its part the INEEL will analyze information from this pilot with the intent to define the Co2 sequestration capacity of coal and its ultimate role in ameliorating the adverse effects of global warming on the nation and the world.

2001-09-30T23:59:59.000Z

328

Coiled tubing drilling with supercritical carbon dioxide  

DOE Patents (OSTI)

A method for increasing the efficiency of drilling operations by using a drilling fluid material that exists as supercritical fluid or a dense gas at temperature and pressure conditions existing at a drill site. The material can be used to reduce mechanical drilling forces, to remove cuttings, or to jet erode a substrate. In one embodiment, carbon dioxide (CO.sub.2) is used as the material for drilling within wells in the earth, where the normal temperature and pressure conditions cause CO.sub.2 to exist as a supercritical fluid. Supercritical carbon dioxide (SC--CO.sub.2) is preferably used with coiled tube (CT) drilling equipment. The very low viscosity SC--CO.sub.2 provides efficient cooling of the drill head, and efficient cuttings removal. Further, the diffusivity of SC--CO.sub.2 within the pores of petroleum formations is significantly higher than that of water, making jet erosion using SC--CO.sub.2 much more effective than water jet erosion. SC--CO.sub.2 jets can be used to assist mechanical drilling, for erosion drilling, or for scale removal. A choke manifold at the well head or mud cap drilling equipment can be used to control the pressure within the borehole, to ensure that the temperature and pressure conditions necessary for CO.sub.2 to exist as either a supercritical fluid or a dense gas occur at the drill site. Spent CO.sub.2 can be vented to the atmosphere, collected for reuse, or directed into the formation to aid in the recovery of petroleum.

Kolle , Jack J. (Seattle, WA)

2002-01-01T23:59:59.000Z

329

Terpolymerization of ethylene, sulfur dioxide and carbon monoxide  

DOE Patents (OSTI)

This invention relates to a high molecular weight terpolymer of ethylene, sulfur dioxide and carbon monoxide stable to 280.degree. C. and containing as little as 36 mol % ethylene and about 41-51 mol % sulfur dioxide; and to the method of producing said terpolymer by irradiation of a liquid and gaseous mixture of ethylene, sulfur dioxide and carbon monoxide by means of Co-60 gamma rays or an electron beam, at a temperature of about 10.degree.-50.degree. C., and at a pressure of about 140 to 680 atmospheres, to initiate polymerization.

Johnson, Richard (Shirley, NY); Steinberg, Meyer (Huntington Station, NY)

1981-01-01T23:59:59.000Z

330

Estimated Carbon Dioxide Emissions in 2008: United States  

Science Conference Proceedings (OSTI)

Flow charts depicting carbon dioxide emissions in the United States have been constructed from publicly available data and estimates of state-level energy use patterns. Approximately 5,800 million metric tons of carbon dioxide were emitted throughout the United States for use in power production, residential, commercial, industrial, and transportation applications in 2008. Carbon dioxide is emitted from the use of three major energy resources: natural gas, coal, and petroleum. The flow patterns are represented in a compact 'visual atlas' of 52 state-level (all 50 states, the District of Columbia, and one national) carbon dioxide flow charts representing a comprehensive systems view of national CO{sub 2} emissions. Lawrence Livermore National Lab (LLNL) has published flow charts (also referred to as 'Sankey Diagrams') of important national commodities since the early 1970s. The most widely recognized of these charts is the U.S. energy flow chart (http://flowcharts.llnl.gov). LLNL has also published charts depicting carbon (or carbon dioxide potential) flow and water flow at the national level as well as energy, carbon, and water flows at the international, state, municipal, and organizational (i.e. United States Air Force) level. Flow charts are valuable as single-page references that contain quantitative data about resource, commodity, and byproduct flows in a graphical form that also convey structural information about the system that manages those flows. Data on carbon dioxide emissions from the energy sector are reported on a national level. Because carbon dioxide emissions are not reported for individual states, the carbon dioxide emissions are estimated using published energy use information. Data on energy use is compiled by the U.S. Department of Energy's Energy Information Administration (U.S. EIA) in the State Energy Data System (SEDS). SEDS is updated annually and reports data from 2 years prior to the year of the update. SEDS contains data on primary resource consumption, electricity generation, and energy consumption within each economic sector. Flow charts of state-level energy usage and explanations of the calculations and assumptions utilized can be found at: http://flowcharts.llnl.gov. This information is translated into carbon dioxide emissions using ratios of carbon dioxide emissions to energy use calculated from national carbon dioxide emissions and national energy use quantities for each particular sector. These statistics are reported annually in the U.S. EIA's Annual Energy Review. Data for 2008 (US. EIA, 2010) was updated in August of 2010. This is the first presentation of a comprehensive state-level package of flow charts depicting carbon dioxide emissions for the United States.

Smith, C A; Simon, A J; Belles, R D

2011-04-01T23:59:59.000Z

331

The Role of Manganese Dioxide (MnO2) Deposition in Microbiologically Influenced Corrosion  

Science Conference Proceedings (OSTI)

This report documents the role of manganese dioxide (MnO2) in microbiologically influenced corrosion.

2004-12-20T23:59:59.000Z

332

Short-Term Energy Outlook Model Documentation: Carbon Dioxide (CO2) Emissions Model  

Reports and Publications (EIA)

Description of the procedures for estimating carbon dioxide emissions in the Short-Term Energy Outlook

Information Center

2009-08-11T23:59:59.000Z

333

Oxidation catalyst  

DOE Patents (OSTI)

The present invention generally relates to catalyst systems and methods for oxidation of carbon monoxide. The invention involves catalyst compositions which may be advantageously altered by, for example, modification of the catalyst surface to enhance catalyst performance. Catalyst systems of the present invention may be capable of performing the oxidation of carbon monoxide at relatively lower temperatures (e.g., 200 K and below) and at relatively higher reaction rates than known catalysts. Additionally, catalyst systems disclosed herein may be substantially lower in cost than current commercial catalysts. Such catalyst systems may be useful in, for example, catalytic converters, fuel cells, sensors, and the like.

Ceyer, Sylvia T. (Cambridge, MA); Lahr, David L. (Cambridge, MA)

2010-11-09T23:59:59.000Z

334

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

335

Innovative Geothermal Startup Will Put Carbon Dioxide To Good Use |  

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

Geothermal Startup Will Put Carbon Dioxide To Good Use Geothermal Startup Will Put Carbon Dioxide To Good Use Innovative Geothermal Startup Will Put Carbon Dioxide To Good Use March 17, 2011 - 2:09pm Addthis A basic overview of GreenFire's process to convert CO2 into electricity. | Photo courtesy of GreenFire. A basic overview of GreenFire's process to convert CO2 into electricity. | Photo courtesy of GreenFire. JoAnn Milliken What does this project do? GreenFire Energy will conduct the first field demonstration of a CO2-based geothermal system. Getting geothermal power with CO2 instead of water would be particularly beneficial in the arid Southwestern U.S., where water is scarce. Geothermal power holds enormous opportunities to provide affordable, clean energy that avoids greenhouse gases like carbon dioxide (CO2). That's

336

Carbon Dioxide Emissions Associated with Bioenergy and Other Biogenic  

Open Energy Info (EERE)

Carbon Dioxide Emissions Associated with Bioenergy and Other Biogenic Carbon Dioxide Emissions Associated with Bioenergy and Other Biogenic Sources Jump to: navigation, search Tool Summary LAUNCH TOOL Name: Carbon Dioxide Emissions Associated with Bioenergy and Other Biogenic Sources Agency/Company /Organization: United States Environmental Protection Agency Sector: Energy, Climate Focus Area: Biomass, - Biomass Combustion, - Biomass Gasification, - Biomass Pyrolysis, - Biofuels, - Landfill Gas, - Waste to Energy, Greenhouse Gas Phase: Evaluate Options Resource Type: Publications, Guide/manual User Interface: Website Website: www.epa.gov/climatechange/emissions/biogenic_emissions.html Cost: Free References: EPA, 40 CFR Part 60[1] Tailoring Rule[2] Biogenic Emissions[3] The 'EPA Climate Change - Green House Gas Emissions - Carbon Dioxide

337

Recycling Carbon Dioxide to Make Plastics | Department of Energy  

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

Recycling Carbon Dioxide to Make Plastics Recycling Carbon Dioxide to Make Plastics Recycling Carbon Dioxide to Make Plastics May 20, 2013 - 1:31pm Addthis Novomerñ€™s thermoplastic pellets incorporate waste CO2 into a variety of consumer products. Novomer's thermoplastic pellets incorporate waste CO2 into a variety of consumer products. Why is this important? By using CO2 that would otherwise be emitted to the atmosphere, the process has the potential to cut greenhouse gas emissions while simultaneously reducing petroleum consumption and producing useful products for American consumers. The world's first successful large-scale production of a polypropylene carbonate (PPC) polymer using waste carbon dioxide (CO2) as a key raw material has resulted from a projected funded in part by the U.S. Department of Energy's Office of Fossil Energy.

338

Carbon Dioxide Sequestration (West Virginia) | Department of Energy  

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

Dioxide Sequestration (West Virginia) Dioxide Sequestration (West Virginia) Carbon Dioxide Sequestration (West Virginia) < Back Eligibility Utility Fed. Government Commercial Agricultural Investor-Owned Utility State/Provincial Govt Industrial Construction Municipal/Public Utility Local Government Residential Installer/Contractor Rural Electric Cooperative Tribal Government Low-Income Residential Schools Retail Supplier Institutional Multi-Family Residential Systems Integrator Fuel Distributor Nonprofit General Public/Consumer Transportation Program Info State West Virginia Program Type Environmental Regulations Fees Safety and Operational Guidelines Siting and Permitting The purpose of this law is to: Establish a legal and regulatory framework for the permitting of carbon dioxide sequestration operations; Designate a state agency responsible for establishing standards and

339

Depleted Uranium Dioxide as SNF Waste Package Fill: A Disposal...  

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

DEPLETED URANIUM DIOXIDE AS SNF WASTE PACKAGE FILL: A DISPOSAL OPTION Charles W. Forsberg Oak Ridge National Laboratory * P.O. Box 2008 Oak Ridge, Tennessee 37831-6179 Tel: (865)...

340

World energy consumption and carbon dioxide emissions : 1950-2050  

E-Print Network (OSTI)

Emissions of carbon dioxide form combustion of fossil fuels, which may contribute to long-term climate change, are projected through 2050 using reduced form models estimated with national-level panel data for the period ...

Schmalensee, Richard

1995-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "dioxide nitrous oxide" 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

Energy-related carbon dioxide emissions down in 2011 - Today ...  

U.S. Energy Information Administration (EIA)

Annual energy-related carbon dioxide (CO 2) emissions fell 2.4% in 2011 compared to the level in 2010. Several factors combined to produce this drop, including slower ...

342

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

343

Control strategies for supercritical carbon dioxide power conversion systems  

E-Print Network (OSTI)

The supercritical carbon dioxide (S-C02) recompression cycle is a promising advanced power conversion cycle which couples well to numerous advanced nuclear reactor designs. This thesis investigates the dynamic simulation ...

Carstens, Nathan, 1978-

2007-01-01T23:59:59.000Z

344

NETL: News Release - DOE Study Monitors Carbon Dioxide Storage...  

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

1, 2009 DOE Study Monitors Carbon Dioxide Storage in Norway's Offshore Sleipner Gas Field U.S. World-Acclaimed Marine Institutes Partner with Europeans in North Sea Washington,...

345

Table 21. Total Energy Related Carbon Dioxide Emissions, Projected...  

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

Total Energy Related Carbon Dioxide Emissions, Projected vs. Actual Projected (million metric tons) 1993 1994 1995 1996 1997 1998 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008...

346

Figure 5. Energy-related carbon dioxide emissions in four ...  

U.S. Energy Information Administration (EIA)

Sheet3 Sheet2 Sheet1 Reference High Oil/Gas Resouce CO2$15 CO2$15HR Released: May 2, 2013 Figure 5. Energy-related carbon dioxide emissions in four ...

347

Ownership of Carbon Dioxide Captured by Clean Coal Project (Texas)  

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

This legislation stipulates that the Railroad Commission of Texas automatically acquires the title to any carbon dioxide captured by a clean coal project in the state. The Bureau of Economic...

348

CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS  

Science Conference Proceedings (OSTI)

This report describes research conducted between October 1, 2004 and December 31, 2004 on the use of dry regenerable sorbents for removal of carbon dioxide from flue gas. Two supported sorbents were tested in a bench scale fluidized bed reactor system. The sorbents were prepared by impregnation of sodium carbonate on to an inert support at a commercial catalyst manufacturing facility. One sorbent, tested through five cycles of carbon dioxide sorption in an atmosphere of 3% water vapor and 0.8 to 3% carbon dioxide showed consistent reactivity with sodium carbonate utilization of 7 to 14%. A second, similarly prepared material, showed comparable reactivity in one cycle of testing. Batches of 5 other materials were prepared in laboratory scale quantities (primarily by spray drying). These materials generally have significantly greater surface areas than calcined sodium bicarbonate. Small scale testing showed no significant adsorption of mercury on representative carbon dioxide sorbent materials under expected flue gas conditions.

David A. Green; Brian S. Turk; Jeffrey W. Portzer; Thomas Nelson; Raghubir P. Gupta

2005-01-01T23:59:59.000Z

349

Cardiac Responses to Carbon Dioxide in Developing Zebrafish (Danio rerio) .  

E-Print Network (OSTI)

??The ontogeny of carbon dioxide (CO2) sensing in zebrafish (Danio rerio) has not been studied. In this thesis, CO2-mediated increases in heart rate were used… (more)

Miller, Scott

2013-01-01T23:59:59.000Z

350

Energy-related carbon dioxide emissions declined in 2012 ...  

U.S. Energy Information Administration (EIA)

Energy-related carbon dioxide (CO 2) emissions in 2012 were the lowest in the United States since 1994, at 5.3 billion metric tons of CO 2 (see figure above).

351

Thermophysical Properties of Carbon Dioxide and CO2-Rich Mixtures...  

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

carbon dioxide (CO 2 ) emissions; and will help maintain the nation's leader- ship in the export of gas turbine equipment. In this NETL-managed project, the National Institute of...

352

DEVELOPMENT AND INTEGRATION OF NEW PROCESSES CONSUMING CARBON DIOXIDE IN  

E-Print Network (OSTI)

. Estimation of Greenhouse Gas Emissions....................................... 6 2. Greenhouse Gas Emissions........................................................ 8 C. Carbon Dioxide ­ A Greenhouse Gas................................................ 9 1. Sources............................................................... 3 B. Greenhouse Effect and Climate Change............................................. 4 1

Pike, Ralph W.

353

Carbon Dioxide Capture from Flue Gas Using Dry Regenerable Sorbents  

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

Mill Road P.O. Box 10940 Pittsburgh, PA 15236 412-386-4966 jose.figueroa@netl.doe.gov Carbon DioxiDe Capture from flue Gas usinG Dry reGenerable sorbents Background Currently...

354

World energy consumption and carbon dioxide emissions : 1950-2050  

E-Print Network (OSTI)

Emissions of carbon dioxide from combustion of fossil fuels, which may contribute to long-term climate change, are projected through 2050 using reduced form models estimated with national-level panel data for the period ...

Schmalensee, Richard.; Stoker, Thomas M.; Judson, Ruth A.

355

Short-Term Energy Carbon Dioxide Emissions Forecasts August 2009  

Reports and Publications (EIA)

Supplement to the Short-Term Energy Outlook. Short-term projections for U.S. carbon dioxide emissions of the three fossil fuels: coal, natural gas, and petroleum.

Information Center

2009-08-11T23:59:59.000Z

356

U.S. Energy-Related Carbon Dioxide Emissions, 2012  

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

Energy-Related Carbon Dioxide Emissions, 2012 October 2013 Independent Statistics & Analysis www.eia.gov U.S. Department of Energy Washington, DC 20585 October 2013 U.S. Energy...

357

Carbon Dioxide-Based Heat Pump Water Heater Research Project  

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

The U.S. Department of Energy is currently conducting research into carbon dioxide (CO2) heat pump water heaters. This project will employ innovative techniques to adapt water heating technology to...

358

Synthesis of Titanium Dioxide by Microwave Solid State Method and ...  

Science Conference Proceedings (OSTI)

In this work, titanium dioxide was synthetized by microwave solid-state ... Properties of Low-Carbon High-strength and Low-yield Ratio Bainitic Steels ... New Methodology of Enhancing Etching Factor of Copper Pattern for Advanced Packages.

359

Annual Energy Outlook 2006 with Projections to 2030 - Carbon Dioxide  

Gasoline and Diesel Fuel Update (EIA)

Carbon Dioxide Emissions Carbon Dioxide Emissions Annual Energy Outlook 2006 with Projections to 2030 Higher Energy Consumption Forecast Increases Carbon Dioxide Emissions Figure 107. Carbn dioxide emissions by sector and fuel, 2004 and 2030 (million metric tons). Having problems, call our National Energy Information Center at 202-586-8800 for help. Figure data CO2 emissions from the combustion of fossil fuels are proportional to fuel consumption. Among fossil fuel types, coal has the highest carbon content, natural gas the lowest, and petroleum in between. In the AEO2006 reference case, the shares of these fuels change slightly from 2004 to 2030, with more coal and less petroleum and natural gas. The combined share of carbon-neutral renewable and nuclear energy is stable from 2004 to 2030 at

360

DOE Seeks Applications for Tracking Carbon Dioxide Storage in Geologic  

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

Applications for Tracking Carbon Dioxide Storage in Applications for Tracking Carbon Dioxide Storage in Geologic Formations DOE Seeks Applications for Tracking Carbon Dioxide Storage in Geologic Formations February 19, 2009 - 12:00pm Addthis Washington, DC -- The U.S. Department of Energy (DOE) today issued a Funding Opportunity Announcement (FOA) to enhance the capability to simulate, track, and evaluate the potential risks of carbon dioxide (CO2) storage in geologic formations. Geologic storage is considered to be a key technological solution to mitigate CO2 emissions and combat climate change. DOE anticipates making multiple project awards under this FOA and, depending on fiscal year 2009 appropriations, may be able to provide up to $24 million to be distributed among selected recipients. This investment is

Note: This page contains sample records for the topic "dioxide nitrous oxide" 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

Carbon Dioxide Capture and Storage Demonstration in Developing Countries:  

Open Energy Info (EERE)

Carbon Dioxide Capture and Storage Demonstration in Developing Countries: Carbon Dioxide Capture and Storage Demonstration in Developing Countries: Analysis of Key Policy Issues and Barriers Jump to: navigation, search Tool Summary LAUNCH TOOL Name: Carbon Dioxide Capture and Storage Demonstration in Developing Countries: Analysis of Key Policy Issues and Barriers Focus Area: Clean Fossil Energy Topics: Potentials & Scenarios Website: cdn.globalccsinstitute.com/sites/default/files/publications/15536/carb Equivalent URI: cleanenergysolutions.org/content/carbon-dioxide-capture-and-storage-de Policies: "Deployment Programs,Financial Incentives" is not in the list of possible values (Deployment Programs, Financial Incentives, Regulations) for this property. DeploymentPrograms: Technical Assistance This report discusses the value of carbon capture and storage (CCS)

362

New and Underutilized Technology: Carbon Dioxide Demand Ventilation Control  

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

Carbon Dioxide Demand Ventilation Carbon Dioxide Demand Ventilation Control New and Underutilized Technology: Carbon Dioxide Demand Ventilation Control October 4, 2013 - 4:23pm Addthis The following information outlines key deployment considerations for carbon dioxide (CO2) demand ventilation control within the Federal sector. Benefits Demand ventilation control systems modulate ventilation levels based on current building occupancy, saving energy while still maintaining proper indoor air quality (IAQ). CO2 sensors are commonly used, but a multiple-parameter approach using total volatile organic compounds (TVOC), particulate matter (PM), formaldehyde, and relative humidity (RH) levels can also be used. CO2 sensors control the outside air damper to reduce the amount of outside air that needs to be conditioned and supplied to the building when

363

Interactions of Plutonium Dioxide with Water and Oxygen-Hydrogen Mixtures  

DOE Green Energy (OSTI)

Pressure-volume-temperature data and mass spectrometric results obtained during exposure of PuO{sub 2} to D{sub 2}O show that the dioxide reacts with water at room temperature to produce a higher oxide (PuO{sub 2+x})and H{sub 2}. Results demonstrate that PuO{sub 2+x} is the thermodynamically stable oxide in air. The absence of O{sub 2} at detectable levels in the gas phase implies that radiolytic decomposition of water to the elements is not a significant reaction. The rate of the PuO{sub 2}+H{sub 2}O reaction is 6{+-}4 nmol H{sub 2}/m{sup 2} day, a value that is independent of the H{sub 2}O concentration on the oxide over a range that extends from fractional monolayer coverage to saturation by liquid water. Evaluation of literature data shows that oxide compositions in excess of PuO{sub 2.25} are attained, but the maximum value of x is unknown. During exposure of PuO{sub 2} to a 2:1 D{sub 2}:O{sub 2} mixture at room temperature, the elements combine by a process consistent with a surface-catalyzed reaction. Water is simultaneously formed by the H{sub 2}+O{sub 2} reaction and consumed by the PuO{sub 2} + H{sub 2}O reaction and accumulates until the opposing rates are equal. Thereafter, PuO{sub 2+x} is formed at a constant rate by the water-catalyzed PuO{sub 2} + O{sub 2} reaction. The failure of earlier attempts to prepare higher oxides of plutonium is discussed and the catalytic cycle that promotes the reaction of PuO{sub 2} with O{sub 2} is described. Implications of the results for extended storage and environmental chemistry of oxide are examined. Moisture-catalyzed oxidation of PuO{sub 2} accounts for observation of both pressure increases and decreases in oxide storage containers with air atmospheres. Application of the experimental rate results indicates that the reaction of a typical oxide with 0.5 mass % of adsorbed water maybe complete after 25 to 50 years at room temperature.

Haschke, J.M.; Allen, T.H.

1999-01-01T23:59:59.000Z

364

Catalytic Transformation of Waste Carbon Dioxide into Valuable Products  

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

Catalytic Transformation of Waste Catalytic Transformation of Waste Carbon Dioxide into Valuable Products Background Many industrial processes contribute large amounts of carbon dioxide (CO 2 ) to the earth's atmosphere. In an effort to reduce the amount of CO 2 released to the atmosphere, the U.S. Department of Energy (DOE) is funding efforts to develop CO 2 capture and storage technologies. In addition to permanent storage of CO 2 in underground reservoirs, some

365

DOE/NETL CarbON DiOxiDE  

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

CarbON DiOxiDE CapTurE aND STOragE rD&D rOaDmap DECEmbEr 2010 ii u.S. DEparTmENT Of ENErgy CarbON DiOxiDE CapTurE aND STOragE rD&D rOaDmap Disclaimer This report was prepared as an...

366

Biofilter for removal of nitrogen oxides from contaminated gases under aerobic conditions  

DOE Patents (OSTI)

A biofilter is described for reducing concentrations of gaseous nitrogen oxides in a polluted gas comprises a porous organic filter bed medium disposed in a housing, the filter bed medium including a mixed culture of naturally occurring denitrifying bacteria for converting the nitrogen oxides to nitrogen gas, carbon dioxide, and water. A method is described of reducing concentrations of nitrogen oxides in polluted gas comprises conducting the polluted gas through the biofilter so that the denitrifying bacteria can degrade the nitrogen oxides. A preferred filter medium is wood compost, however composts of other organic materials are functional. Regulation of pH, moisture content, exogenous carbon sources, and temperature are described. 6 figs.

Apel, W.A.

1998-08-18T23:59:59.000Z

367

Biofilter for removal of nitrogen oxides from contaminated gases under aerobic conditions  

DOE Patents (OSTI)

A biofilter for reducing concentrations of gaseous nitrogen oxides in a polluted gas comprises a porous organic filter bed medium disposed in a housing, the filter bed medium including a mixed culture of naturally occurring denitrifying bacteria for converting the nitrogen oxides to nitrogen gas, carbon dioxide, and water. A method of reducing concentrations of nitrogen oxides in polluted gas comprises conducting the polluted gas through the biofilter so that the denitrifying bacteria can degrade the nitrogen oxides. A preferred filter medium is wood compost, however composts of other organic materials are functional. Regulation of pH, moisture content, exogenous carbon sources, and temperature are described.

Apel, William A. (Idaho Falls, ID)

1998-01-01T23:59:59.000Z

368

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

369

Carbon dioxide sequestration: When and how much  

E-Print Network (OSTI)

We analyze carbon dioxide (CO sequestration as a strategy to manage future climate change in an optimal economic growth framework. We approach the problem in two ways: first, by using a simple analytical model, and second, by using a numerical optimization model which allows us to explore the problem in a more realistic setting. CO sequestration is not a perfect substitute for avoiding CO2 production because CO2 leaks back to the atmosphere and hence imposes future costs. The “efficiency factor ” of CO2 sequestration can be expressed as the ratio of the avoided emissions to the economically equivalent amount of sequestered CO2 emissions. A simple analytical model in terms of a net-present value criterion suggests that short-term sequestration methods such as afforestation can be somewhat ( 60 %) efficient, while long term sequestration (such as deep aquifer or deep ocean sequestration) can be very ( 90%) efficient. A numerical study indicates that CO2 sequestration methods at a cost within the range of present estimates reduce the economically optimal CO2 concentrations and climate related damages. The potential savings associated with CO2 sequestration is equivalent in our utilitarian model to a one-time investment of several percent of present gross world product. 1 1

Klaus Keller; Zili Yang; Matt Hall; David F. Bradford

2003-01-01T23:59:59.000Z

370

Why sequence carbon monoxide oxidizing thermophiles?  

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

carbon monoxide oxidizing thermophiles? carbon monoxide oxidizing thermophiles? Many microbes that use carbon monoxide as an energy source are found in high temperature environments such as geothermal areas. Researchers think that these carboxydotrophs may be involved in reducing potentially toxic carbon monoxide hotspots by combine with water to form hydrogen, carbon dioxide and acetate, which are in turn used for thermophilic energy conservation and carbon sequestration mechanisms. The project focuses on sequencing two closely related microbes, one of which is Carboxydothermus hydrogenformans. A strain of C. hydrogenformans has been grown in hydrogen-enriched synthesis gas (syngas), which contains a mix of hydrogen and carbon monoxide. Researchers are interested in sequencing both microbial strains to track the genome's evolution and

371

Uranium Oxide Aerosol Transport in Porous Graphite  

Science Conference Proceedings (OSTI)

The objective of this paper is to investigate the transport of uranium oxide particles that may be present in carbon dioxide (CO2) gas coolant, into the graphite blocks of gas-cooled, graphite moderated reactors. The transport of uranium oxide in the coolant system, and subsequent deposition of this material in the graphite, of such reactors is of interest because it has the potential to influence the application of the Graphite Isotope Ratio Method (GIRM). The GIRM is a technology that has been developed to validate the declared operation of graphite moderated reactors. GIRM exploits isotopic ratio changes that occur in the impurity elements present in the graphite to infer cumulative exposure and hence the reactor’s lifetime cumulative plutonium production. Reference Gesh, et. al., for a more complete discussion on the GIRM technology.

Blanchard, Jeremy; Gerlach, David C.; Scheele, Randall D.; Stewart, Mark L.; Reid, Bruce D.; Gauglitz, Phillip A.; Bagaasen, Larry M.; Brown, Charles C.; Iovin, Cristian; Delegard, Calvin H.; Zelenyuk, Alla; Buck, Edgar C.; Riley, Brian J.; Burns, Carolyn A.

2012-01-23T23:59:59.000Z

372

Carbon Dioxide-Water Emulsions for Enhanced Oil Recovery and Permanent Sequestration of Carbon Dioxide  

Science Conference Proceedings (OSTI)

This project involves the use of an innovative new invention ? Particle Stabilized Emulsions (PSEs) of Carbon Dioxide-in-Water and Water-in-Carbon Dioxide for Enhanced Oil Recovery (EOR) and Permanent Sequestration of Carbon Dioxide. The EOR emulsion would be injected into a semi-depleted oil reservoir such as Dover 33 in Otsego County, Michigan. It is expected that the emulsion would dislocate the stranded heavy crude oil from the rock granule surfaces, reduce its viscosity, and increase its mobility. The advancing emulsion front should provide viscosity control which drives the reduced-viscosity oil toward the production wells. The make-up of the emulsion would be subsequently changed so it interacts with the surrounding rock minerals in order to enhance mineralization, thereby providing permanent sequestration of the injected CO{sub 2}. In Phase 1 of the project, the following tasks were accomplished: 1. Perform laboratory scale (mL/min) refinements on existing procedures for producing liquid carbon dioxide-in-water (C/W) and water-in-liquid carbon dioxide (W/C) emulsion stabilized by hydrophilic and hydrophobic fine particles, respectively, using a Kenics-type static mixer. 2. Design and cost evaluate scaled up (gal/min) C/W and W/C emulsification systems to be deployed in Phase 2 at the Otsego County semi-depleted oil field. 3. Design the modifications necessary to the present CO{sub 2} flooding system at Otsego County for emulsion injection. 4. Design monitoring and verification systems to be deployed in Phase 2 for measuring potential leakage of CO{sub 2} after emulsion injection. 5. Design production protocol to assess enhanced oil recovery with emulsion injection compared to present recovery with neat CO{sub 2} flooding. 6. Obtain Federal and State permits for emulsion injection. Initial research focused on creating particle stabilized emulsions with the smallest possible globule size so that the emulsion can penetrate even low-permeability crude oilcontaining formations or saline aquifers. The term ?globule? refers to the water or liquid carbon dioxide droplets sheathed with ultrafine particles dispersed in the continuous external medium, liquid CO{sub 2} or H{sub 2}O, respectively. The key to obtaining very small globules is the shear force acting on the two intermixing fluids, and the use of ultrafine stabilizing particles or nanoparticles. We found that using Kenics-type static mixers with a shear rate in the range of 2700 to 9800 s{sup -1} and nanoparticles between 100-300 nm produced globule sizes in the 10 to 20 ?m range. Particle stabilized emulsions with that kind of globule size should easily penetrate oil-bearing formations or saline aquifers where the pore and throat size can be on the order of 50 ?m or larger. Subsequent research focused on creating particle stabilized emulsions that are deemed particularly suitable for Permanent Sequestration of Carbon Dioxide. Based on a survey of the literature an emulsion consisting of 70% by volume of water, 30% by volume of liquid or supercritical carbon dioxide, and 2% by weight of finely pulverized limestone (CaCO{sub 3}) was selected as the most promising agent for permanent sequestration of CO{sub 2}. In order to assure penetration of the emulsion into tight formations of sandstone or other silicate rocks and carbonate or dolomite rock, it is necessary to use an emulsion consisting of the smallest possible globule size. In previous reports we described a high shear static mixer that can create such small globules. In addition to the high shear mixer, it is also necessary that the emulsion stabilizing particles be in the submicron size, preferably in the range of 0.1 to 0.2 ?m (100 to 200 nm) size. We found a commercial source of such pulverized limestone particles, in addition we purchased under this DOE Project a particle grinding apparatus that can provide particles in the desired size range. Additional work focused on attempts to generate particle stabilized emulsions with a flow through, static mixer based apparatus under a variety

Ryan, David; Golomb, Dan; Shi, Guang; Shih, Cherry; Lewczuk, Rob; Miksch, Joshua; Manmode, Rahul; Mulagapati, Srihariraju; Malepati, Chetankurmar

2011-09-30T23:59:59.000Z

373

The growth and evolution of thin oxide films on delta-plutonium surfaces  

Science Conference Proceedings (OSTI)

The common oxides of plutonium are the dioxide (PuO{sub 2}) and the sesquioxide (Pu{sub 2}O{sub 3}). The structure of an oxide on plutonium metal under air at room temperature is typically described as a thick PuO{sub 2} film at the gas-oxide interface with a thinner PuO{sub 2} film near the oxide-metal substrate interface. In a reducing environment, such as ultra high vacuum, the dioxide (Pu{sup 4+}; O/Pu = 2.0) readily converts to the sesquioxide (Pu{sup 3+}; O/Pu = 1.5) with time. In this work, the growth and evolution of thin plutonium oxide films is studied with x-ray photoelectron spectroscopy (XPS) under varying conditions. The results indicate that, like the dioxide, the sesquioxide is not stable on a very clean metal substrate under reducing conditions, resulting in substoichiometric films (Pu{sub 2}O{sub 3-y}). The Pu{sub 2}O{sub 3-y} films prepared exhibit a variety of stoichiometries (y = 0.2-1) as a function of preparation conditions, highlighting the fact that caution must be exercised when studying plutonium oxide surfaces under these conditions and interpreting resulting data.

Garcia Flores, Harry G [Los Alamos National Laboratory; Pugmire, David L [Los Alamos National Laboratory

2009-01-01T23:59:59.000Z

374

Ionic Liquid Membranes for Carbon Dioxide Separation  

SciTech Connect

Recent scientific studies are rapidly advancing novel technological improvements and engineering developments that demonstrate the ability to minimize, eliminate, or facilitate the removal of various contaminants and green house gas emissions in power generation. The Integrated Gasification Combined Cycle (IGCC) shows promise for carbon dioxide mitigation not only because of its higher efficiency as compared to conventional coal firing plants, but also due to a higher driving force in the form of high partial pressure. One of the novel technological concepts currently being developed and investigated is membranes for carbon dioxide (CO2) separation, due to simplicity and ease of scaling. A challenge in using membranes for CO2 capture in IGCC is the possibility of failure at elevated temperatures or pressures. Our earlier research studies examined the use of ionic liquids on various supports for CO2 separation over the temperature range, 37°C-300°C. The ionic liquid, 1-hexyl-3methylimidazolium Bis(trifluoromethylsulfonyl)imide, ([hmim][Tf2N]), was chosen for our initial studies with the following supports: polysulfone (PSF), poly(ether sulfone) (PES), and cross-linked nylon. The PSF and PES supports had similar performance at room temperature, but increasing temperature caused the supported membranes to fail. The ionic liquid with the PES support greatly affected the glass transition temperature, while with the PSF, the glass transition temperature was only slightly depressed. The cross-linked nylon support maintained performance without degradation over the temperature range 37-300°C with respect to its permeability and selectivity. However, while the cross-linked nylon support was able to withstand temperatures, the permeability continued to increase and the selectivity decreased with increasing temperature. Our studies indicated that further testing should examine the use of other ionic liquids, including those that form chemical complexes with CO2 based on amine interactions. The hypothesis is that the performance at the elevated temperatures could be improved by allowing a facilitated transport mechanism to become dominant. Several amine-based ionic liquids were tested on the cross-linked nylon support. It was found that using the amine-based ionic liquid did improve selectivity and permeability at higher temperature. The hypothesis was confirmed, and it was determined that the type of amine used also played a role in facilitated transport. Given the appropriate aminated ionic liquid with the cross-linked nylon support, it is possible to have a membrane capable of separating CO2 at IGCC conditions. With this being the case, the research has expanded to include separation of other constituents besides CO2 (CO, H2S, etc.) and if they play a role in membrane poisoning or degradation. This communication will discuss the operation of the recently fabricated ionic liquid membranes and the impact of gaseous components other than CO2 on their performance and stability.

Myers, C.R.; Ilconich, J.B.; Luebke, D.R.; Pennline, H.W.

2008-07-12T23:59:59.000Z

375

Thermal oxidation vitrification flue gas elimination system  

SciTech Connect

With minor modifications to a Best Demonstrated Available Technology hazardous waste incinerator, it is possible to obtain combustion without potentially toxic emissions by using technology currently employed in similar applications throughout industry. Further, these same modifications will reduce waste handling over an extended operating envelope while minimizing energy consumption. Three by-products are produced: industrial grade carbon dioxide, nitrogen, and a final waste form that will exceed Toxicity Characteristics Leaching Procedures requirements and satisfy nuclear waste product consistency tests. The proposed system utilizes oxygen rather than air as an oxidant to reduce the quantities of total emissions, improve the efficiency of the oxidation reactions, and minimize the generation of toxic NO{sub x} emissions. Not only will less potentially hazardous constituents be generated; all toxic substances can be contained and the primary emission, carbon dioxide -- the leading ``greenhouse gas`` contributing to global warming -- will be converted to an industrial by-product needed to enhance the extraction of energy feedstocks from maturing wells. Clearly, the proposed configuration conforms to the provisions for Most Achievable Control Technology as defined and mandated for the private sector by the Clear Air Act Amendments of 1990 to be implemented in 1997 and still lacking definition.

Kephart, W. [Foster-Wheeler Environmental Corp., Oak Ridge, TN (United States); Angelo, F. [Resource Energy Corp. (United States); Clemens, M. [Argonne National Lab., IL (United States)

1995-06-01T23:59:59.000Z

376

Carbon-dioxide-controlled ventilation study  

Science Conference Proceedings (OSTI)

The In-House Energy Management (IHEM) Program has been established by the U.S. Department of Energy to provide funds to federal laboratories to conduct research on energy-efficient technology. The Energy Sciences Department of Pacific Northwest Laboratory (PNL) was tasked by IHEM to research the energy savings potential associated with reducing outdoor-air ventilation of buildings. By monitoring carbon dioxide (CO{sub 2}) levels in a building, outdoor air provided by the heating, ventilating, and air-conditioning (HVAC) system can be reduced to the percentage required to maintain satisfactory CO{sub 2} levels rather than ventilating with a higher outdoor-air percentage based on an arbitrary minimum outdoor-air setting. During summer months, warm outdoor air brought into a building for ventilation must be cooled to meet the appropriate cooling supply-air temperature, and during winter months, cold outdoor air must be heated. By minimizing the amount of hot or cold outdoor air brought into the HVAC system, the supply air requires less cooling or heating, saving energy and money. Additionally, the CO{sub 2} levels in a building can be monitored to ensure that adequate outdoor air is supplied to a building to maintain air quality levels. The two main considerations prior to implementing CO{sub 2}-based ventilation control are its impact on energy consumption and the adequacy of indoor air quality (IAQ) and occupant comfort. To address these considerations, six portable CO{sub 2} monitors were placed in several Hanford Site buildings to estimate the adequacy of office/workspace ventilation. The monitors assessed the potential for reducing the flow of outdoor-air to the buildings. A candidate building was also identified to monitor various ventilation control strategies for use in developing a plan for implementing and assessing energy savings.

McMordie, K.L.; Carroll, D.M.

1994-05-01T23:59:59.000Z

377

Gas Analysis of Plutonium Materials Tested in a Bell Jar  

SciTech Connect

Seventy cans containing plutonium bearing materials have been tested for gas generation in bell jars at the Savannah River Site (SRS). Gas samples from five of the tests were taken and analyzed for hydrogen, oxygen, nitrogen, methane, carbon dioxide, carbon monoxide, and nitrous oxide. Gas samples from all five cans showed significant oxygen consumption. Hydrogen and carbon dioxide were found in non-negligible quantities in all gas samples. Hydrogen and carbon dioxide generation rates are presented along with oxygen depletion rates. A description of the plutonium bearing materials is also provided.

Kies, J.

2003-04-15T23:59:59.000Z

378

THE HIGH TEMPERATURE BEHAVIOR OF METALLIC INCLUSIONS IN URANIUM DIOXIDE.  

E-Print Network (OSTI)

State of Irradiated Uranium- Plutonium Oxide Fuel Pins,"Ingots Formed in Uranium-Plutonium Oxide Irradiated in EBR-Roake, "Fission Products and Plutonium Migration in Uranium-

Yang, Rosa Lu.

2010-01-01T23:59:59.000Z

379

New Texas Oil Project Will Help Keep Carbon Dioxide Underground |  

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

Texas Oil Project Will Help Keep Carbon Dioxide Underground Texas Oil Project Will Help Keep Carbon Dioxide Underground New Texas Oil Project Will Help Keep Carbon Dioxide Underground February 5, 2013 - 12:05pm Addthis The Air Products and Chemicals hydrogen production facilities in Port Arthur, Texas, is funded by the Energy Department through the 2009 Recovery Act. It is managed by the Office of Fossil Energyñ€™s National Energy Technology Laboratory. | Photo credit Air Products and Chemicals hydrogen production facilities. The Air Products and Chemicals hydrogen production facilities in Port Arthur, Texas, is funded by the Energy Department through the 2009 Recovery Act. It is managed by the Office of Fossil Energy's National Energy Technology Laboratory. | Photo credit Air Products and Chemicals hydrogen

380

NETL: News Release - DOE Report Assesses Potential for Carbon Dioxide  

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

4, 2009 4, 2009 DOE Report Assesses Potential for Carbon Dioxide Storage Beneath Federal Lands Newly Released Document Complements 2008 Carbon Sequestration Atlas Washington, D.C. - As a complementary document to the U.S. Department of Energy's Carbon Sequestration Atlas of the United States and Canada issued in November 2008, the Office of Fossil Energy's National Energy Technology Laboratory has now released a report that provides an initial estimate of the potential to store carbon dioxide (CO2) underneath millions of acres of Federal lands. MORE INFO Read the report The report, Storage of Captured Carbon Dioxide Beneath Federal Lands, estimates and characterizes the storage potential that lies beneath some of the more than 400 million acres of Federal land available for lease.

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381

New Texas Oil Project Will Help Keep Carbon Dioxide Underground |  

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

New Texas Oil Project Will Help Keep Carbon Dioxide Underground New Texas Oil Project Will Help Keep Carbon Dioxide Underground New Texas Oil Project Will Help Keep Carbon Dioxide Underground February 5, 2013 - 12:05pm Addthis The Air Products and Chemicals hydrogen production facilities in Port Arthur, Texas, is funded by the Energy Department through the 2009 Recovery Act. It is managed by the Office of Fossil Energyñ€™s National Energy Technology Laboratory. | Photo credit Air Products and Chemicals hydrogen production facilities. The Air Products and Chemicals hydrogen production facilities in Port Arthur, Texas, is funded by the Energy Department through the 2009 Recovery Act. It is managed by the Office of Fossil Energy's National Energy Technology Laboratory. | Photo credit Air Products and Chemicals hydrogen

382

Geologic Carbon Dioxide Storage Field Projects Supported by DOE's  

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

Geologic Carbon Dioxide Storage Field Projects Supported by DOE's Geologic Carbon Dioxide Storage Field Projects Supported by DOE's Sequestration Program Geologic Carbon Dioxide Storage Field Projects Supported by DOE's Sequestration Program Background: The U.S. DOE's Sequestration Program began with a small appropriation of $1M in 1997 and has grown to be the largest most comprehensive CCS R&D program in the world. The U.S. DOE's sequestration program has supported a number of projects implementing CO2 injection in the United States and other countries including, Canada, Algeria, Norway, Australia, and Germany. The program has also been supporting a number of complementary R&D projects investigating the science of storage, simulation, risk assessment, and monitoring the fate of the injected CO2 in the subsurface.

383

Underground storage of natural gas, liquid hydrocarbons, and carbon dioxide  

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

storage of natural gas, liquid hydrocarbons, and carbon storage of natural gas, liquid hydrocarbons, and carbon dioxide (Louisiana) Underground storage of natural gas, liquid hydrocarbons, and carbon dioxide (Louisiana) < Back Eligibility Commercial Construction Industrial Investor-Owned Utility Municipal/Public Utility Utility Program Info State Louisiana Program Type Environmental Regulations Siting and Permitting The Louisiana Department of Environmental Quality regulates the underground storage of natural gas or liquid hydrocarbons and carbon dioxide. Prior to the use of any underground reservoir for the storage of natural gas and prior to the exercise of eminent domain by any person, firm, or corporation having such right under laws of the state of Louisiana, the commissioner, shall have found all of the following:

384

Supercritical Carbon Dioxide / Reservoir Rock Chemical Interactions | Open  

Open Energy Info (EERE)

Supercritical Carbon Dioxide / Reservoir Rock Chemical Interactions Supercritical Carbon Dioxide / Reservoir Rock Chemical Interactions Jump to: navigation, search Geothermal Lab Call Projects for Supercritical Carbon Dioxide / Reservoir Rock Chemical Interactions Loading map... {"format":"googlemaps3","type":"ROADMAP","types":["ROADMAP","SATELLITE","HYBRID","TERRAIN"],"limit":200,"offset":0,"link":"all","sort":[""],"order":[],"headers":"show","mainlabel":"","intro":"","outro":"","searchlabel":"\u2026 further results","default":"","geoservice":"google","zoom":false,"width":"600px","height":"350px","centre":false,"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":"","icon":"","visitedicon":"","forceshow":true,"showtitle":true,"hidenamespace":false,"template":false,"title":"","label":"","lines":[],"polygons":[],"circles":[],"rectangles":[],"locations":[{"text":"

385

Means and method for reducing carbon dioxide to a product  

SciTech Connect

A method is described for reducing carbon dioxide to a product comprising the steps of: providing carbon dioxide to a catholyte chamber of a reaction cell; providing water to an anolyte section of the reaction cell, forming a passageway through the reaction cell with a dual porosity cathode between the passageway and catholyte chamber and with a porous anode between the passageway and anolyte chamber; provides an electrolyte in a manner so that it passes through the passageway; and provides a direct current voltage across the dual porosity cathode and anode so as to cause a reduction of the carbon dioxide in cooperation with the electrolyte and hydrogen ions passing through the anode. This passes to a product contained within the electrolyte and causes oxygen to be emitted from the anolyte chamber.

Ang, P.G.P.; Sammels, A.F.

1987-06-16T23:59:59.000Z

386

CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS  

SciTech Connect

This report describes research conducted between April 1, 2004 and June 30, 2004 on the preparation and use of dry regenerable sorbents for removal of carbon dioxide from flue gas. Support materials and supported sorbents were prepared by spray drying. Sorbents consisting of 20 to 50% sodium carbonate on a ceramic support were prepared by spray drying in batches of approximately 300 grams. The supported sorbents exhibited greater carbon dioxide capture rates than unsupported calcined sodium bicarbonate in laboratory tests. Preliminary process design and cost estimation for a retrofit application suggested that costs of a dry regenerable sodium carbonate-based process could be lower than those of a monoethanolamine absorption system. In both cases, the greatest part of the process costs come from power plant output reductions due to parasitic consumption of steam for recovery of carbon dioxide from the capture medium.

David A. Green; Brian S. Turk; Jeffrey W. Portzer; Raghubir P. Gupta; William J. McMichael; Thomas Nelson

2004-07-01T23:59:59.000Z

387

Total Carbon Dioxide, Hydrographic, and Nitrate Measurements in the  

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

Total Carbon Dioxide, Hydrographic, and Nitrate Measurements in the Southwest Pacific during Austral Autumn, 1990: Results from NOAA/PMEL CGC-90 Cruise. Total Carbon Dioxide, Hydrographic, and Nitrate Measurements in the Southwest Pacific during Austral Autumn, 1990: Results from NOAA/PMEL CGC-90 Cruise. NDP-052 (1995) data Download the Data and ASCII Documentation files of NDP-052 PDF Download a PDF of NDP-052 image Contributed by Marilyn F. Lamb and Richard A. Feely Pacific Marine Environmental Laboratory Seattle, Washington and Lloyd Moore and Donald K. Atwood Atlantic Oceanographic and Meteorological Laboratory Miami, Florida Prepared by Alexander Kozyr* Carbon Dioxide Information Analysis Center Oak Ridge National Laboratory Oak Ridge, Tennessee, U.S.A. *Energy, Environment, and Resources Center The University of Tennessee Knoxville, Tennessee Environmental Sciences Division Publication No. 4420 Date Published: September 1995

388

Gas Generation Testing of Plutonium Dioxide  

DOE Green Energy (OSTI)

Hydrogen and oxygen gas generation rates were measured for purified plutonium oxide (PuO2) powder as a function of water content, specific surface area (SSA), dose rate, and initial fill gas composition. Gas generation rates were found to increase with water content and dose rate and to decrease with specific surface area for given water content. Hydrogen generation rates were similar in air, nitrogen and argon, but oxygen generation rates were greater in nitrogen and argon than in air. The potential for reaching a steady state container pressure for PuO2 of given calcination temperature (i.e., SSA) and water content was evaluated by adding hydrogen to some test vessels and monitoring the effect on container pressure over time

Duffey, J.M.

2002-08-29T23:59:59.000Z

389

Building Technologies Office: Carbon Dioxide-Based Heat Pump Water Heater  

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

Carbon Dioxide-Based Carbon Dioxide-Based Heat Pump Water Heater Research Project to someone by E-mail Share Building Technologies Office: Carbon Dioxide-Based Heat Pump Water Heater Research Project on Facebook Tweet about Building Technologies Office: Carbon Dioxide-Based Heat Pump Water Heater Research Project on Twitter Bookmark Building Technologies Office: Carbon Dioxide-Based Heat Pump Water Heater Research Project on Google Bookmark Building Technologies Office: Carbon Dioxide-Based Heat Pump Water Heater Research Project on Delicious Rank Building Technologies Office: Carbon Dioxide-Based Heat Pump Water Heater Research Project on Digg Find More places to share Building Technologies Office: Carbon Dioxide-Based Heat Pump Water Heater Research Project on AddThis.com...

390

SunShot Initiative: Supercritical Carbon Dioxide Turbo-Expander and Heat  

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

Supercritical Carbon Dioxide Supercritical Carbon Dioxide Turbo-Expander and Heat Exchangers to someone by E-mail Share SunShot Initiative: Supercritical Carbon Dioxide Turbo-Expander and Heat Exchangers on Facebook Tweet about SunShot Initiative: Supercritical Carbon Dioxide Turbo-Expander and Heat Exchangers on Twitter Bookmark SunShot Initiative: Supercritical Carbon Dioxide Turbo-Expander and Heat Exchangers on Google Bookmark SunShot Initiative: Supercritical Carbon Dioxide Turbo-Expander and Heat Exchangers on Delicious Rank SunShot Initiative: Supercritical Carbon Dioxide Turbo-Expander and Heat Exchangers on Digg Find More places to share SunShot Initiative: Supercritical Carbon Dioxide Turbo-Expander and Heat Exchangers on AddThis.com... Concentrating Solar Power Systems Components

391

Global Patterns of Carbon Dioxide Emissions from Soils on a 0...  

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

Potter. 1996. Global Patterns of Carbon Dioxide Emissions from Soils on a 0.5 Degree Grid Cell Basis. DB-1015. Carbon Dioxide Information Analysis Center, U.S. Department of...

392

THE PATH OF CARBON IN PHOTOSYNTHESIS. X. CARBON DIOXIDE ASSIMILATION IN PLANTS  

E-Print Network (OSTI)

48 The Fath of Carbon i n Photosynthesis X. Carbon Dioxide658 THE PATH O CBRBQM I N PHOTOSYNTHESIS F x CA~ON DIOXIDEr e a c t i o n s of photosynthesis (phosphoglycera t e and

1950-01-01T23:59:59.000Z

393

Electrochemistry of . . . ELECTRODES WITH APPLICATIONS TO FUEL CELLS AND CARBON DIOXIDE CONVERSION DEVICES  

E-Print Network (OSTI)

There is a growing awareness of the need for basic and applied energy research due to the environmental impact of energy use and limitations in the supply of energy sources. In this work, electrochemical research is reported for fuel cells and carbon dioxide reduction, with the aim of reducing the environmental footprint of global energy use. In studies of the formic acid fuel cell, it is reported here that an increase in the formic acid fuel pH increases the rate of formic acid oxidation on palladium and platinum. It is also shown that an increase in fuel pH decreases the potential at which the catalyst poison is removed from the electrode surface. This poison is detrimental to fuel cell operation. This work reports the first such studies in an electrochemical cell on high surface area platinum and palladium nanoparticles. New catalyst formulations were developed via electrochemical surface modification in attempt to eliminate the catalyst poisoning and improve performance of the formic acid fuel cell. Electrochemical studies showed substantial improvement to the rate of formic acid oxidation by a combination of high surface area palladium with tin,

John Leonard Haan

2010-01-01T23:59:59.000Z

394

Statement on global climate change before the Subcommittee on Energy and Power, United States House of Representatives  

SciTech Connect

Greenhouse gases are gases which are effectively transparent to incoming sunlight but absorb infrared radiation escaping to space and thereby warm the surface of the Earth. Human activities result in the release of greenhouse and related gases in such quantities that they are changing the composition of the atmosphere. Greenhouse and related gases which human activities release include carbon dioxide (CO{sub 2}), methane (CH{sub 4}) carbon monoxide (CO), nitrous oxide (N{sub 2}O), nitrogen oxides (NO{sub x}), chlorofluorocarbons (CFCs) and sulphur dioxide (SO{sub 2}). The emission and effects of these gases are detailed in this report.

Edmonds, J.A.

1993-04-01T23:59:59.000Z

395

Standard test methods for chemical and mass spectrometric analysis of nuclear-grade gadolinium oxide (Gd2O3) powder  

E-Print Network (OSTI)

1.1 These test methods cover procedures for the chemical and mass spectrometric analysis of nuclear-grade gadolinium oxide powders to determine compliance with specifications. 1.2 The analytical procedures appear in the following order: Sections Carbon by Direct CombustionThermal Conductivity C1408 Test Method for Carbon (Total) in Uranium Oxide Powders and Pellets By Direct Combustion-Infrared Detection Method Total Chlorine and Fluorine by Pyrohydrolysis Ion Selective Electrode C1502 Test Method for Determination of Total Chlorine and Fluorine in Uranium Dioxide and Gadolinium Oxide Loss of Weight on Ignition 7-13 Sulfur by CombustionIodometric Titration Impurity Elements by a Spark-Source Mass Spectrographic C761 Test Methods for Chemical, Mass Spectrometric, Spectrochemical,Nuclear, and Radiochemical Analysis of Uranium Hexafluoride C1287 Test Method for Determination of Impurities In Uranium Dioxide By Inductively Coupled Plasma Mass Spectrometry Gadolinium Content in Gadolinium Oxid...

American Society for Testing and Materials. Philadelphia

2006-01-01T23:59:59.000Z

396

Solar Power To Help Convert Carbon Dioxide Into Fuel : Renewable Energy News  

E-Print Network (OSTI)

Solar Power To Help Convert Carbon Dioxide Into Fuel : Renewable Energy News TUESDAY 25 MAY, 2010 | | Solar Power To Help Convert Carbon Dioxide Into Fuel by Energy Matters Microbiologist Derek Lovley dioxide into transportation fuels, with the help of special micro-organisms and solar power. The team

Lovley, Derek

397

of carbon dioxide containing 12 but the low concentration of 14  

E-Print Network (OSTI)

of carbon dioxide containing 12 C and 13 C, but the low concentration of 14 C has made its measurement in carbon dioxide extremely difficult. Using an ultrasensitive technique called saturated carbon at values well below radiocarbon's natural abundance in carbon dioxide. In their technique

Zare, Richard N.

398

Carbon Dioxide Footprint of the Northwest Power System Comments submitted by Grant County Public Utility District  

E-Print Network (OSTI)

Carbon Dioxide Footprint of the Northwest Power System Comments submitted by Grant County Public paper: Carbon Dioxide Footprint of the Northwest Power System, dated September 13, 2007. The Grant done a very thorough job of assessing the current and future carbon dioxide footprints of the Northwest

399

Lipid Oxidation Pathways  

Science Conference Proceedings (OSTI)

This book reviews state-of-the-art developments in the understanding of the oxidation of lipids and its connection with the oxidation of other biological molecules such as proteins and starch. Lipid Oxidation Pathways Hardback Books Health - Nutrition -

400

Carbonation Mechanism of Reservoir Rock by Supercritical Carbon Dioxide  

Open Energy Info (EERE)

Carbonation Mechanism of Reservoir Rock by Supercritical Carbon Dioxide Carbonation Mechanism of Reservoir Rock by Supercritical Carbon Dioxide Geothermal Lab Call Project Jump to: navigation, search Last modified on July 22, 2011. Project Title Carbonation Mechanism of Reservoir Rock by Supercritical Carbon Dioxide Project Type / Topic 1 Laboratory Call for Submission of Applications for Research, Development and Analysis of Geothermal Technologies Project Type / Topic 2 Supercritical Carbon Dioxide / Reservoir Rock Chemical Interactions Project Description Supercritical CO2 is currently becoming a more common fluid for extracting volatile oil and fragrance compounds from various raw materials that are used in perfumery. Furthermore, its use as a heat transmission fluid is very attractive because of the greater uptake capability of heat from hot reservoir rock, compared with that of water. However, one concern was the reactivity of CO2 with clay and rock minerals in aqueous and non-aqueous environments. So if this reaction leads to the formation of water-soluble carbonates, such formation could be detrimental to the integrity of wellbore infrastructure.

Note: This page contains sample records for the topic "dioxide nitrous oxide" 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

EIA - International Energy Outlook 2007-Energy-Related Carbon Dioxide  

Gasoline and Diesel Fuel Update (EIA)

7 7 Figure 77. World Energy-Related Carbon Dioxide Emissions by Region, 2003-2030 Figure 77 Data. Need help, contact the National Energy Information Center at 202-586-8800. Figure 78. World Energy-Related Carbon Dioxide Emissions by Fuel Type, 1990-2030 Figure 78 Data. Need help, contact the National Energy Information Center at 202-586-8800. Figure 79. Average Annual Growth in Energy-Related Carbon Dioxide Emissions in the OECD Economies, 2004-2030 Figure 79 Data. Need help, contact the National Energy Information Center at 202-586-8800. Figure 80. Average Annual Growth in Energy-Related Carbon Dioide Emissions in the Non-OECD Economies, 2004-2030 Figure 80 Data. Need help, contact the National Energy Information Center at 202-586-8800. Figure 81. World Carbon Dioxide Emissions from Liquids Combustion by Region, 1990-2030 Figure 81 Data. Need help, contact the National Energy Information Center at 202-586-8800.

402

EIA - International Energy Outlook 2008-Energy-Related Carbon Dioxide  

Gasoline and Diesel Fuel Update (EIA)

8 8 Figure 75. World Energy-Related Carbon Dioxide Emissions, 2005-2030 Figure 75 Data. Need help, contact the National Energy Information Center at 202-586-8800. Figure 76. World Energy-Related Carbon Dioxide Emissions by Fuel Type, 1990-2030 Figure 76 Data. Need help, contact the National Energy Information Center at 202-586-8800. Figure 77. Average Annual Growth in Energy-Related Carbon Dioxide Emissions in the OECD Economies, 2005-2030 Figure 77 Data. Need help, contact the National Energy Information Center at 202-586-8800. Figure 78. U.S. Energy-Related Carbon Dioide Emissions in IEO2007 and IEO2008, 2005-2030 Figure 78 Data. Need help, contact the National Energy Information Center at 202-586-8800. Figure 79. Average Annual Growth in Energy-Related Carbon Dioxide Emissions in the Non-OECD Economies, 2005-2030 Figure 79 Data. Need help, contact the National Energy Information Center at 202-586-8800.

403

Cobalt carbonyl catalyzed olefin hydroformylation in supercritical carbon dioxide  

DOE Patents (OSTI)

A method of olefin hydroformylation is provided wherein an olefin reacts with a carbonyl catalyst and with reaction gases such as hydrogen and carbon monoxide in the presence of a supercritical reaction solvent, such as carbon dioxide. The invention provides higher yields of n-isomer product without the gas-liquid mixing rate limitation seen in conventional Oxo processes using liquid media.

Rathke, J.W.; Klingler, R.J.

1992-12-31T23:59:59.000Z

404

Regulation and Permitting of Carbon Dioxide Geologic Sequestration Wells  

Science Conference Proceedings (OSTI)

This report provides an update of the United States’ regulations and project experiences associated with permitting injection wells used for geologic sequestration of carbon dioxide (CO2). This report is an update of a previous Electric Power Research Institute (EPRI) study on this subject published in December 2008 when the draft regulations governing geologic sequestration were first published.BackgroundSeparating ...

2013-12-18T23:59:59.000Z

405

Groundwater Chemistry Changes as a Result of Carbon Dioxide Injection  

Science Conference Proceedings (OSTI)

This report provides final results from a combined field, laboratory, and modeling investigation into whether carbon dioxide (CO2) can have an adverse impact on potable groundwater. The investigation was undertaken by the Electric Power Research Institute (EPRI), Lawrence Berkeley National Laboratory, United States Geological Survey (USGS), and Montana State University (MSU).

2009-12-23T23:59:59.000Z

406

Cobalt carbonyl catalyzed olefin hydroformylation in supercritical carbon dioxide  

DOE Patents (OSTI)

A method of olefin hydroformylation is provided wherein an olefin reacts with a carbonyl catalyst and with reaction gases such as hydrogen and carbon monoxide in the presence of a supercritical reaction solvent, such as carbon dioxide. The invention provides higher yields of n-isomer product without the gas-liquid mixing rate limitation seen in conventional Oxo processes using liquid media.

Rathke, Jerome W. (Lockport, IL); Klingler, Robert J. (Westmount, IL)

1993-01-01T23:59:59.000Z

407

II. Greenhouse gas markets, carbon dioxide credits and biofuels17  

E-Print Network (OSTI)

or biodiesel use in Europe. Nevertheless, the EU directive sets a target for the use of biofuels15 II. Greenhouse gas markets, carbon dioxide credits and biofuels17 The previous chapter analysed mandatory blends and utilization targets as policy measures that can provide incentives for expanded

408

Phase relation between global temperature and atmospheric carbon dioxide  

E-Print Network (OSTI)

The primary ingredient of Anthropogenic Global Warming hypothesis is the assumption that atmospheric carbon dioxide variations are the cause for temperature variations. In this paper we discuss this assumption and analyze it on basis of bi-centenary measurements and using a relaxation model which causes phase shifts and delays.

Stallinga, Peter

2013-01-01T23:59:59.000Z

409

Cobalt carbonyl catalyzed olefin hydroformylation in supercritical carbon dioxide  

DOE Patents (OSTI)

A method of olefin hydroformylation is provided wherein an olefin reacts with a carbonyl catalyst and with reaction gases such as hydrogen and carbon monoxide in the presence of a supercritical reaction solvent, such as carbon dioxide. The invention provides higher yields of n-isomer product without the gas-liquid mixing rate limitation seen in conventional Oxo processes using liquid media.

Rathke, J.W.; Klingler, R.J.

1993-03-30T23:59:59.000Z

410

Carbon dioxide flash-freezing applied to ice cream production  

E-Print Network (OSTI)

(cont.) Carbon dioxide is recompressed from 1.97 x 106 Pa (285 psi) to 3.96 x 106 Pa (575 psi). The process is scaled by increasing the number of nozzles to accommodate the desired flow rate. Only 165 nozzles are required ...

Peters, Teresa Baker, 1981-

2006-01-01T23:59:59.000Z

411

Corrosion of various engineering alloys in supercritical carbon dioxide  

E-Print Network (OSTI)

The corrosion resistance of ten engineering alloys were tested in a supercritical carbon dioxide (S-CO 2) environment for up to 3000 hours at 610°C and 20MPa. The purpose of this work was to evaluate each alloy as a potential ...

Gibbs, Jonathan Paul

2010-01-01T23:59:59.000Z

412

Reducing Emissions of Sulfur Dioxide, Nitrogen Oxides, and Mercury from Electric Power Plants  

Reports and Publications (EIA)

This analysis responds to a request from Senators Bob Smith, George Voinovich, and Sam Brownback to examine the costs of specific multi-emission reduction strategies

J. Alan Beamon

2001-10-01T23:59:59.000Z

413

Selective methane oxidation over promoted oxide catalysts  

DOE Green Energy (OSTI)

Objective was to selectively oxidize methane to C{sub 2} hydrocarbons and to oxygenates, in particular formaldehyde and methanol, in high space time yields under relatively mild reaction conditions. Results in this document are reported under the headings: methane oxidation over silica, methane oxidation over Sr/La{sub 2}O{sub 3} catalysts, and oxidative coupling of methane over sulfate-doped Sr/La{sub 2}O{sub 3} catalysts. 24 refs, 10 figs, 4 tabs.

Klier, K.; Herman, R.G.

1993-12-31T23:59:59.000Z

414

EVALUATION OF PROTON-CONDUCTING MEMBRANES FOR USE IN A SULFUR-DIOXIDE DEPOLARIZED ELECTROLYZER  

DOE Green Energy (OSTI)

The chemical stability, sulfur dioxide transport, ionic conductivity, and electrolyzer performance have been measured for several commercially available and experimental proton exchange membranes (PEMs) for use in a sulfur dioxide depolarized electrolyzer (SDE). The SDE's function is to produce hydrogen by using the Hybrid Sulfur (HyS) Process, a sulfur based electrochemical/thermochemical hybrid cycle. Membrane stability was evaluated using a screening process where each candidate PEM was heated at 80 C in 60 wt. % H{sub 2}SO{sub 4} for 24 hours. Following acid exposure, chemical stability for each membrane was evaluated by FTIR using the ATR sampling technique. Membrane SO{sub 2} transport was evaluated using a two-chamber permeation cell. SO{sub 2} was introduced into one chamber whereupon SO{sub 2} transported across the membrane into the other chamber and oxidized to H{sub 2}SO{sub 4} at an anode positioned immediately adjacent to the membrane. The resulting current was used to determine the SO{sub 2} flux and SO{sub 2} transport. Additionally, membrane electrode assemblies (MEAs) were prepared from candidate membranes to evaluate ionic conductivity and selectivity (ionic conductivity vs. SO{sub 2} transport) which can serve as a tool for selecting membranes. MEAs were also performance tested in a HyS electrolyzer measuring current density versus a constant cell voltage (1V, 80 C in SO{sub 2} saturated 30 wt% H2SO{sub 4}). Finally, candidate membranes were evaluated considering all measured parameters including SO{sub 2} flux, SO{sub 2} transport, ionic conductivity, HyS electrolyzer performance, and membrane stability. Candidate membranes included both PFSA and non-PFSA polymers and polymer blends of which the non-PFSA polymers, BPVE-6F and PBI, showed the best selectivity.

Hobbs, D.; Elvington, M.; Colon-Mercado, H.

2009-11-11T23:59:59.000Z

415

Reduction of Carbon Dioxide inAqueous Solutions by IonizingRadiation  

DOE Green Energy (OSTI)

The question of the conditions under which living matter originated on the surface of the earth is still a subject limited largely to speculation. The speculation has a greater chance of approaching the truth insofar as it includes and is based upon the ever wider variety of established scientific fact. One of the purposes of the herein reported observation was to add another fact to the ever increasing information which might have any bearing upon this most interesting question. It is not our purpose in the present communication to discuss the various proposals or the arguments which have been adduced for and against them. One of the most popular current conceptions is that life originated in an organic milieu on the surface of the earth, (1,2,3,4,5). The problem to which we are addressed is the origin of that organic milieu in the absence of any life. It appeared to us that one source, if not the only source, of reduced carbon compounds in complex arrangements might be the interaction of various high energy radiations with aqueous solutions of inorganic materials, particularly carbon dioxide, and nitrogenous compounds such as ammonia and nitrogen, since it appears that these compounds were the commoner forms in which the essential elements found themselves on the primordial earth. While it has long been known that high energy radiations can cause organic decomposition and oxidation, it seemed useful to us to demonstrate that conditions could be found in which high energy radiations could induce the reduction with water of carbon dioxide and the ultimate creation of polyatomic molecules (other than simple polymerization of monomers) of carbon, oxygen, hydrogen and nitrogen.

Garrison, W.M.; Morrison, D.C.; Hamilton, J.G.; Benson, A.A.; Calvin, M.

1951-03-13T23:59:59.000Z

416

C:\mydocs\WPDOCS\1605B\Electric_eia3.PDF  

Gasoline and Diesel Fuel Update (EIA)

Updated Updated State-level Greenhouse Gas Emission Factors for Electricity Generation March 2001 Energy Information Administration Office of Integrated Analysis and Forecasting Energy Information Administration U.S. Department of Energy Energy Information Administration / Updated State-level Greenhouse Gas Emission Factors for Electricity Generation i TABLE OF CONTENTS 1. INTRODUCTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1 2. UPDATED EMISSIONS COEFFICIENTS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 Carbon Dioxide . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 Nitrous Oxide and Methane . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

417

Supercritical carbon dioxide cycle control analysis.  

SciTech Connect

This report documents work carried out during FY 2008 on further investigation of control strategies for supercritical carbon dioxide (S-CO{sub 2}) Brayton cycle energy converters. The main focus of the present work has been on investigation of the S-CO{sub 2} cycle control and behavior under conditions not covered by previous work. An important scenario which has not been previously calculated involves cycle operation for a Sodium-Cooled Fast Reactor (SFR) following a reactor scram event and the transition to the primary coolant natural circulation and decay heat removal. The Argonne National Laboratory (ANL) Plant Dynamics Code has been applied to investigate the dynamic behavior of the 96 MWe (250 MWt) Advanced Burner Test Reactor (ABTR) S-CO{sub 2} Brayton cycle following scram. The timescale for the primary sodium flowrate to coast down and the transition to natural circulation to occur was calculated with the SAS4A/SASSYS-1 computer code and found to be about 400 seconds. It is assumed that after this time, decay heat is removed by the normal ABTR shutdown heat removal system incorporating a dedicated shutdown heat removal S-CO{sub 2} pump and cooler. The ANL Plant Dynamics Code configured for the Small Secure Transportable Autonomous Reactor (SSTAR) Lead-Cooled Fast Reactor (LFR) was utilized to model the S-CO{sub 2} Brayton cycle with a decaying liquid metal coolant flow to the Pb-to-CO{sub 2} heat exchangers and temperatures reflecting the decaying core power and heat removal by the cycle. The results obtained in this manner are approximate but indicative of the cycle transient performance. The ANL Plant Dynamics Code calculations show that the S-CO{sub 2} cycle can operate for about 400 seconds following the reactor scram driven by the thermal energy stored in the reactor structures and coolant such that heat removal from the reactor exceeds the decay heat generation. Based on the results, requirements for the shutdown heat removal system may be defined. In particular, the peak heat removal capacity of the shutdown heat removal loop may be specified to be 1.1 % of the nominal reactor power. An investigation of the oscillating cycle behavior calculated by the ANL Plant Dynamics Code under specific conditions has been carried out. It has been found that the calculation of unstable operation of the cycle during power reduction to 0 % may be attributed to the modeling of main compressor operation. The most probable reason for such instabilities is the limit of applicability of the currently used one-dimensional compressor performance subroutines which are based on empirical loss coefficients. A development of more detailed compressor design and performance models is required and is recommended for future work in order to better investigate and possibly eliminate the calculated instabilities. Also, as part of such model development, more reliable surge criteria should be developed for compressor operation close to the critical point. It is expected that more detailed compressor models will be developed as a part of validation of the Plant Dynamics Code through model comparison with the experiment data generated in the small S-CO{sub 2} loops being constructed at Barber-Nichols Inc. and Sandia National Laboratories (SNL). Although such a comparison activity had been planned to be initiated in FY 2008, data from the SNL compression loop currently in operation at Barber Nichols Inc. has not yet become available by the due date of this report. To enable the transient S-CO{sub 2} cycle investigations to be carried out, the ANL Plant Dynamics Code for the S-CO{sub 2} Brayton cycle was further developed and improved. The improvements include further optimization and tuning of the control mechanisms as well as an adaptation of the code for reactor systems other than the Lead-Cooled Fast Reactor (LFR). Since the focus of the ANL work on S-CO{sub 2} cycle development for the majority of the current year has been on the applicability of the cycle to SFRs, work has started on modification of the ANL Plant Dynamics Code to allow

Moisseytsev, A.; Sienicki, J. J. (Nuclear Engineering Division)

2011-04-11T23:59:59.000Z

418

Abatement of Air Pollution: Control of Carbon Dioxide Emissions/Carbon  

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

Carbon Dioxide Carbon Dioxide Emissions/Carbon Dioxide Budget Trading Program (Connecticut) Abatement of Air Pollution: Control of Carbon Dioxide Emissions/Carbon Dioxide Budget Trading Program (Connecticut) < Back Eligibility Agricultural Commercial Construction Fed. Government Fuel Distributor General Public/Consumer Industrial Installer/Contractor Institutional Investor-Owned Utility Local Government Low-Income Residential Multi-Family Residential Municipal/Public Utility Nonprofit Residential Retail Supplier Rural Electric Cooperative Schools State/Provincial Govt Systems Integrator Transportation Tribal Government Utility Savings Category Alternative Fuel Vehicles Hydrogen & Fuel Cells Buying & Making Electricity Water Home Weatherization Solar Wind Program Info State Connecticut

419

Vehicle Technologies Office: Fact #478: July 16, 2007 U.S. Carbon Dioxide  

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

8: July 16, 2007 8: July 16, 2007 U.S. Carbon Dioxide Emissions by Sector to someone by E-mail Share Vehicle Technologies Office: Fact #478: July 16, 2007 U.S. Carbon Dioxide Emissions by Sector on Facebook Tweet about Vehicle Technologies Office: Fact #478: July 16, 2007 U.S. Carbon Dioxide Emissions by Sector on Twitter Bookmark Vehicle Technologies Office: Fact #478: July 16, 2007 U.S. Carbon Dioxide Emissions by Sector on Google Bookmark Vehicle Technologies Office: Fact #478: July 16, 2007 U.S. Carbon Dioxide Emissions by Sector on Delicious Rank Vehicle Technologies Office: Fact #478: July 16, 2007 U.S. Carbon Dioxide Emissions by Sector on Digg Find More places to share Vehicle Technologies Office: Fact #478: July 16, 2007 U.S. Carbon Dioxide Emissions by Sector on AddThis.com...

420

Fundamentals of Mercury Oxidation in Flue Gas  

SciTech Connect

The objective of this project is to understand the importance of and the contribution of gas-phase and solid-phase coal constituents in the mercury oxidation reactions. The project involves both experimental and modeling efforts. The team is comprised of the University of Utah, Reaction Engineering International, and the University of Connecticut. The objective is to determine the experimental parameters of importance in the homogeneous and heterogeneous oxidation reactions; validate models; and, improve existing models. Parameters to be studied include HCl, NO{sub x}, and SO{sub 2} concentrations, ash constituents, and temperature. This report summarizes Year 3 results for the experimental and modeling tasks. Experiments have been completed on the effects of chlorine. However, the experiments with sulfur dioxide and NO, in the presence of water, suggest that the wet-chemistry analysis system, namely the impingers, is possibly giving erroneous results. Future work will investigate this further and determine the role of reactions in the impingers on the oxidation results. The solid-phase experiments have not been completed and it is anticipated that only preliminary work will be accomplished during this study.

JoAnn S. Lighty; Geoffrey Silcox; Andrew Fry; Joseph Helble; Balaji Krishnakumar

2006-07-31T23:59:59.000Z

Note: This page contains sample records for the topic "dioxide nitrous oxide" 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

Solid Oxide Fuel Cell Power Generation Systems  

Science Conference Proceedings (OSTI)

An increasing worldwide demand for premium power, emerging trend towards electric utility deregulation and distributed power generation, global environmental concerns and regulatory controls have accelerated the development of advanced fuel cell based power generation systems. Fuel cells convert chemical energy to electrical energy through electrochemical oxidation of gaseous and/or liquid fuels ranging from hydrogen to hydrocarbons. Electrochemical oxidation of fuels prevents the formation of Nox, while the higher efficiency of the systems reduces carbon dioxide emissions (kg/kWh). Among various fuel cell power generation systems currently being developed for stationary and mobile applications, solid oxide fuel cells (SOFC) offer higher efficiency (up to 80% overall efficiency in hybrid configurations), fuel flexibility, tolerance to CO poisoning, modularity, and use of non-noble construction materials of low strategic value. Tubular, planar, and monolithic cell and stack configurations are currently being developed for stationary and military applications. The current generation of fuel cells uses doped zirconia electrolyte, nickel cermet anode, doped Perovskite cathode electrodes and predominantly ceramic interconnection materials. Fuel cells and cell stacks operate in a temperature range of 800-1000 *C. Low cost ($400/kWe), modular (3-10kWe) SOFC technology development approach of the Solid State Energy Conversion Alliance (SECA) initiative of the USDOE will be presented and discussed. SOFC technology will be reviewed and future technology development needs will be addressed.

Singh, Prabhakar; Pederson, Larry R.; Simner, Steve P.; Stevenson, Jeffry W.; Viswanathan, Vish V.

2001-05-12T23:59:59.000Z

422

Photo-oxidation catalysts  

DOE Patents (OSTI)

Photo-oxidation catalysts and methods for cleaning a metal-based catalyst are disclosed. An exemplary catalyst system implementing a photo-oxidation catalyst may comprise a metal-based catalyst, and a photo-oxidation catalyst for cleaning the metal-based catalyst in the presence of light. The exposure to light enables the photo-oxidation catalyst to substantially oxidize absorbed contaminants and reduce accumulation of the contaminants on the metal-based catalyst. Applications are also disclosed.

Pitts, J. Roland (Lakewood, CO); Liu, Ping (Irvine, CA); Smith, R. Davis (Golden, CO)

2009-07-14T23:59:59.000Z

423

Integrating catalytic coal gasifiers with solid oxide fuel cells  

Science Conference Proceedings (OSTI)

A review was conducted for coal gasification technologies that integrate with solid oxide fuel cells (SOFC) to achieve system efficiencies near 60% while capturing and sequestering >90% of the carbon dioxide [1-2]. The overall system efficiency can reach 60% when a) the coal gasifier produces a syngas with a methane composition of roughly 25% on a dry volume basis, b) the carbon dioxide is separated from the methane-rich synthesis gas, c) the methane-rich syngas is sent to a SOFC, and d) the off-gases from the SOFC are recycled back to coal gasifier. The thermodynamics of this process will be reviewed and compared to conventional processes in order to highlight where available work (i.e. exergy) is lost in entrained-flow, high-temperature gasification, and where exergy is lost in hydrogen oxidation within the SOFC. The main advantage of steam gasification of coal to methane and carbon dioxide is that the amount of exergy consumed in the gasifier is small compared to conventional, high temperature, oxygen-blown gasifiers. However, the goal of limiting the amount of exergy destruction in the gasifier has the effect of limiting the rates of chemical reactions. Thus, one of the main advantages of steam gasification leads to one of its main problems: slow reaction kinetics. While conventional entrained-flow, high-temperature gasifiers consume a sizable portion of the available work in the coal oxidation, the consumed exergy speeds up the rates of reactions. And while the rates of steam gasification reactions can be increased through the use of catalysts, only a few catalysts can meet cost requirements because there is often significant deactivation due to chemical reactions between the inorganic species in the coal and the catalyst. Previous research into increasing the kinetics of steam gasification will be reviewed. The goal of this paper is to highlight both the challenges and advantages of integrating catalytic coal gasifiers with SOFCs.

Siefert, N.; Shamsi, A.; Shekhawat, D.; Berry, D.

2010-01-01T23:59:59.000Z

424

Development of Geologic Storage Estimates for Carbon Dioxide  

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

the Methodology for the Methodology for Development of Geologic Storage Estimates for Carbon Dioxide Prepared for U.S. Department of Energy National Energy Technology Laboratory Carbon Storage Program September 2010 Summary of the Methodology for Development of Geologic Storage Estimates for Carbon Dioxide 2 Authors: U.S. Department of Energy, National Energy Technology Laboratory/ Strategic Center for Coal/Office of Coal and Power R&D John Litynski U.S. Department of Energy, National Energy Technology Laboratory/ Strategic Center for Coal/Office of Coal and Power R&D/Sequestration Division Dawn Deel Traci Rodosta U. S. Department of Energy, National Energy Technology Laboratory/ Office of Research and Development George Guthrie U. S. Department of Energy, National Energy Technology Laboratory/

425

Cermet Waste Packages Using Depleted Uranium Dioxide and Steel  

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

CERMET WASTE PACKAGES USING DEPLETED URANIUM DIOXIDE AND STEEL CERMET WASTE PACKAGES USING DEPLETED URANIUM DIOXIDE AND STEEL Charles W. Forsberg Oak Ridge National Laboratory * P.O. Box 2008 Oak Ridge, Tennessee 37831-6180 Tel: (865) 574-6783 Fax: (865) 574-9512 Email: forsbergcw@ornl.gov Manuscript Number: 078 File Name: DuCermet.HLWcon01.article.final Article Prepared for 2001 International High-Level Radioactive Waste Management Conference American Nuclear Society Las Vegas, Nevada April 29-May 3, 2001 Limits: 1500 words; 3 figures Actual: 1450 words; 3 figures Session: 3.6 Disposal Container Materials and Designs The submitted manuscript has been authored by a contractor of the U.S. Government under contract DE-AC05-00OR22725. Accordingly, the U.S. Government retains a nonexclusive, royalty-free license to publish or reproduce the published form of this contribution,

426

Optimal Geological Enviornments for Carbon Dioxide Storage in Saline Formations  

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

susan D. Hovorka susan D. Hovorka Principal Investigator University of Texas at Austin Bureau of Economic Geology 10100 Burnet Road, Bldg. 130 P.O. Box X Austin, TX 78713 512-471-4863 susan.hovorka@beg.utexas.edu Optimal GeOlOGical envirOnments fOr carbOn DiOxiDe stOraGe in saline fOrmatiOns Background For carbon dioxide (CO 2 ) sequestration to be a successful component of the United States emissions reduction strategy, there will have to be a favorable intersection of a number of factors, such as the electricity market, fuel source, power plant design and operation, capture technology, a suitable geologic sequestration site, and a pipeline right-of-way from the plant to the injection site. The concept of CO 2 sequestration in saline water-bearing formations (saline reservoirs), isolated at

427

Estimation of Carbon Credits in Carbon Dioxide Sequestration Activities  

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

Carbon Credits in Carbon Credits in Carbon Dioxide Sequestration Activities K. Thomas Klasson and Brian H. Davison Oak Ridge National Laboratory * Oak Ridge, Tennessee 37831-6226 Presentation First National Conference on Carbon Sequestration May 14-17, 2001 Washington, DC "The submitted manuscript has been authored by a contractor of the U.S. Government under contract No. DE-AC05-00OR22725. Accordingly, the U.S. Government retains a nonexclusive, royalty-free license to publish or reproduce the published form of this contribution, or allow others to do so, for U.S. Government purposes." * Managed by UT-Battelle, LLC, for the U.S. Department of Energy under contract DE-AC05-00OR22725 1 Estimation of Carbon Credits in Carbon Dioxide Sequestration Activities

428

NETL: Demonstration of a Novel Supercritical Carbon Dioxide Power Cycle  

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

Oxy-Combustion CO2 Emissions Control Oxy-Combustion CO2 Emissions Control Demonstration of a Novel Supercritical Carbon Dioxide Power Cycle Utilizing Pressurized Oxy-Combustion in Conjunction with Cryogenic Compression Project No.: DE-FE0009395 Southwest Research Institute (SwRI) is developing a novel supercritical carbon dioxide (sCO2) advanced power system utilizing pressurized oxy-combustion in conjunction with cryogenic compression. The proposed power system offers a leap in overall system efficiency while producing an output stream of sequestration ready CO2 at pipeline pressures. The system leverages developments in pressurized oxy-combustion technology and recent developments in sCO2 power cycles to achieve high net cycle efficiencies and produce CO2 at pipeline pressures without requiring additional compression of the flue gas.

429

Modelling interactions of carbon dioxide, forests, and climate  

SciTech Connect

Atmospheric carbon dioxide is rising and forests and climate is changing! This combination of fact and premise may be evaluated at a range of temporal and spatial scales with the aid of computer simulators describing the interrelationships between forest vegetation, litter and soil characteristics, and appropriate meteorological variables. Some insights on the effects of climate on the transfers of carbon and the converse effect of carbon transfer on climate are discussed as a basis for assessing the significance of feedbacks between vegetation and climate under conditions of rising atmospheric carbon dioxide. Three main classes of forest models are reviewed. These are physiologically-based models, forest succession simulators based on the JABOWA model, and ecosystem-carbon budget models that use compartment transfer rates with empirically estimated coefficients. Some regression modeling approaches are also outlined. Energy budget models applied to forests and grasslands are also reviewed. This review presents examples of forest models; a comprehensive discussion of all available models is not undertaken.

Luxmoore, R.J. [Oak Ridge National Lab., TN (United States); Baldocchi, D.D. [National Oceanic and Atmospheric Administration, Oak Ridge, TN (United States)

1994-09-01T23:59:59.000Z

430

CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS  

SciTech Connect

Electrobalance studies of calcination and carbonation of sodium bicarbonate materials were conducted at Louisiana State University. Calcination in an inert atmosphere was rapid and complete at 120 C. Carbonation was temperature dependent, and both the initial rate and the extent of reaction were found to decrease as temperature was increased between 60 and 80 C. A fluidization test apparatus was constructed at RTI and two sodium bicarbonate materials were fluidized in dry nitrogen at 22 C. The bed was completely fluidized at between 9 and 11 in. of water pressure drop. Kinetic rate expression derivations and thermodynamic calculations were conducted at RTI. Based on literature data, a simple reaction rate expression, which is zero order in carbon dioxide and water, was found to provide the best fit against reciprocal temperature. Simulations based on process thermodynamics suggested that approximately 26 percent of the carbon dioxide in flue gas could be recovered using waste heat available at 240 C.

David A. Green; Brian S. Turk; Raghubir P. Gupta; Alejandro Lopez-Ortiz; Douglas P. Harrison; Ya Liang

2001-05-01T23:59:59.000Z

431

Regenerable Immobilized Aminosilane Sorbents for Carbon Dioxide Capture  

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

Immobilized Aminosilane Sorbents Immobilized Aminosilane Sorbents for Carbon Dioxide Capture Opportunity Research is currently active on the patent-pending technology titled "Regenerable Immobilized Aminosilane Sorbents for Carbon Dioxide Capture." The technology is available for licensing and/or further collaborative research from the U.S. Department of Energy's National Energy Technology Laboratory. Overview Carbon sequestration entails a multi-step process in which CO 2 is first separated / captured from gas streams followed by permanent storage. Carbon capture represents a critical step in the process and accounts for a considerable portion of the overall cost. Newly developed, high capacity amine-based sorbents offer many advantages over existing technology including increased CO

432

Electro Catalytic Oxidation (ECO) Operation  

Science Conference Proceedings (OSTI)

The power industry in the United States is faced with meeting many new regulations to reduce a number of air pollutants including sulfur dioxide, nitrogen oxides, fine particulate matter, and mercury. With over 1,000 power plants in the US, this is a daunting task. In some cases, traditional pollution control technologies such as wet scrubbers and SCRs are not feasible. Powerspan's Electro-Catalytic Oxidation, or ECO{reg_sign} process combines four pollution control devices into a single integrated system that can be installed after a power plant's particulate control device. Besides achieving major reductions in emissions of sulfur dioxide (SO{sub 2}), nitrogen oxides (NOx), fine particulate matter (PM2.5) and mercury (Hg), ECO produces a highly marketable fertilizer, which can help offset the operating costs of the process system. Powerspan has been operating a 50-MW ECO commercial demonstration unit (CDU) at FirstEnergy Corp.'s R.E. Burger Plant near Shadyside, Ohio, since February 2004. In addition to the CDU, a test loop has been constructed beside the CDU to demonstrate higher NOx removal rates and test various scrubber packing types and wet ESP configurations. Furthermore, Powerspan has developed the ECO{reg_sign}{sub 2} technology, a regenerative process that uses a proprietary solvent to capture CO{sub 2} from flue gas. The CO{sub 2} capture takes place after the capture of NOx, SO{sub 2}, mercury, and fine particulate matter. Once the CO{sub 2} is captured, the proprietary solution is regenerated to release CO{sub 2} in a form that is ready for geological storage or beneficial use. Pilot scale testing of ECO{sub 2} began in early 2009 at FirstEnergy's Burger Plant. The ECO{sub 2} pilot unit is designed to process a 1-MW flue gas stream and produce 20 tons of CO{sub 2} per day, achieving a 90% CO{sub 2} capture rate. The ECO{sub 2} pilot program provided the opportunity to confirm process design and cost estimates, and prepare for large scale capture and sequestration projects. The objectives of this project were to prove at a commercial scale that ECO is capable of extended operations over a range of conditions, that it meets the reliability requirements of a typical utility, and that the fertilizer co-product can be consistently generated, providing ECO with an economic advantage over conventional technologies currently available. Further objectives of the project were to show that the ECO system provides flue gas that meets the inlet standards necessary for ECO{sub 2} to operate, and that the outlet CO{sub 2} and other constituents produced by the ECO{sub 2} pilot can meet Kinder-Morgan pipeline standards for purposes of sequestration. All project objectives are consistent with DOE's Pollution Control Innovations for Power Plants program goals.

Morgan Jones

2011-03-31T23:59:59.000Z

433

Regulation and Permitting of Carbon Dioxide Transport and Geologic Sequestration  

Science Conference Proceedings (OSTI)

This report provides a comprehensive review and analysis of United States (U.S.) regulations that will have a direct impact on permitting and commercial-scale deployment of carbon dioxide (CO2) transport and sequestration projects. The report focuses on specific regulations associated with CO2 transport and sequestration, including pipeline regulations and the U.S. Environmental Protection Agency's (EPA's) proposed rules for characterizing, operating, monitoring, and closing CO2 geologic sequestration we...

2008-12-16T23:59:59.000Z

434

Carbon Dioxide Separation with Supported Ionic Liquid Membranes  

DOE Green Energy (OSTI)

Supported liquid membranes are a class of materials that allow the researcher to utilize the wealth of knowledge available on liquid properties as a direct guide in the development of a capture technology. These membranes also have the advantage of liquid phase diffusivities higher than those observed in polymeric membranes which grant proportionally greater permeabilities. The primary shortcoming of the supported liquid membranes demonstrated in past research has been the lack of stability caused by volatilization of the transport liquid. Ionic liquids, which possess high carbon dioxide solubility relative to light gases such as hydrogen, are an excellent candidate for this type of membrane since they have negligible vapor pressure and are not susceptible to evaporation. A study has been conducted evaluating the use of several ionic liquids, including 1-hexyl-3-methyl-imidazolium bis(trifuoromethylsulfonyl)imide, 1-butyl-3-methyl-imidazolium nitrate, and 1-ethyl-3-methyl-imidazolium sulfate in supported ionic liquid membranes for the capture of carbon dioxide from streams containing hydrogen. In a joint project, researchers at the University of Notre Dame lent expertise in ionic liquid synthesis and characterization, and researchers at the National Energy Technology Laboratory incorporated candidate ionic liquids into supports and evaluated the resulting materials for membrane performance. Initial results have been very promising with carbon dioxide permeabilities as high as 950 barrers and significant improvements in carbon dioxide/hydrogen selectivity over conventional polymers at 37C and at elevated temperatures. Results include a comparison of the performance of several ionic liquids and a number of supports as well as a discussion of innovative fabrication techniques currently under development.

Luebke, D.R.; Ilconich, J.B.; Myers, C.R.; Pennline, H.W.

2007-04-01T23:59:59.000Z

435

RADIATION SYNTHESIS OF CARBON DIOXIDE IN ICE-COATED CARBON: IMPLICATIONS FOR INTERSTELLAR GRAINS AND ICY MOONS  

Science Conference Proceedings (OSTI)

We report the synthesis of carbon dioxide on an amorphous carbon-13 substrate coated with amorphous water ice from irradiation with 100 keV protons at 20 K and 120 K. The quantitative studies show that the CO{sub 2} is dispersed in the ice; its column density increases with ion fluence to a maximum value (in 10{sup 15} molecules cm{sup -2}) of {approx}1 at 20 K and {approx}3 at 120 K. The initial yield is 0.05 (0.1) CO{sub 2} per incident H{sup +} at 20 (120) K. The CO{sub 2} destruction process, which limits the maximum column density, occurs with an effective cross section of {approx}2.5 (4.1) Multiplication-Sign 10{sup -17} cm{sup 2} at 20 (120) K. We discuss radiation-induced oxidation by reactions of radicals in water with the carbon surface and demonstrate that these reactions can be a significant source of condensed carbon dioxide in interstellar grains and in icy satellites in the outer solar system.

Raut, U.; Fulvio, D.; Baragiola, R. A. [Laboratory for Atomic and Surface Physics, University of Virginia, Thornton Hall, Charlottesville, VA 22904 (United States); Loeffler, M. J. [Astrochemistry Laboratory, NASA Goddard Space Flight Center, Mail Code 69, Greenbelt, MD 20771 (United States)

2012-06-20T23:59:59.000Z

436

A High Pressure Carbon Dioxide Separation Process for IGCC Plants  

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

High Pressure Carbon Dioxide Separation Process for IGCC Plants High Pressure Carbon Dioxide Separation Process for IGCC Plants 1 A High Pressure Carbon Dioxide Separation Process for IGCC Plants S.S. Tam 1 , M.E. Stanton 1 , S. Ghose 1 , G. Deppe 1 , D.F. Spencer 2 , R.P. Currier 3 , J.S. Young 3 , G.K. Anderson 3 , L.A. Le 3 , and D.J. Devlin 3 1 Nexant, Inc. (A Bechtel Technology & Consulting Company) 45 Fremont St., 7 th Fl., San Francisco, CA 94506 2 SIMTECHE 13474 Tierra Heights Road, Redding, CA 96003 3 Los Alamos National Laboratory P.O. Box 1663 (MS J567), Los Alamos, NM 87545 1.0 INTRODUCTION Under separate contracts from the U.S. Department of Energy, Office of Fossil Energy (DOE- FE), Los Alamos National Laboratory, and a team of SIMTECHE and Nexant (a Bechtel Technology and Consulting Company) are jointly working to develop the proprietary process for

437

A methodology for forecasting carbon dioxide flooding performance  

E-Print Network (OSTI)

A methodology was developed for forecasting carbon dioxide (CO2) flooding performance quickly and reliably. The feasibility of carbon dioxide flooding in the Dollarhide Clearfork "AB" Unit was evaluated using the methodology. This technique is very helpful when time and data resources are limited. The methodology consists of five tasks: 1) select a section of the reservoir with the most detailed geologic, reservoir, and production data, 2) perform material balance analysis for the selected section to determine 001? and the history of total expansion, voidage, and injectage, 3) establish an average 5-spot pattern within the selected section, 4) develop a black oil numerical simulation model for a quarter of the 5-spot pattern and simulate the primary and waterflood recovery processes, and 5) forecast carbon dioxide performance using Shell's Scoping model, Texaco's "PROPHET" model, and VIP miscible simulator. One of the major limitations of the methodology is that details of individual well performance and reservoir pressure and fluid saturation distributions in the project area are not available. Therefore, the forecast is limited to the average pattern and to the reservoir as a whole. Results of the Dollarhide Clearfork simulation study show that 9.7 % to 14.1 % of OOIP may be recovered by C02 flood in the selected section. It would require WAG injection cycles with a total fluid injection of 0.831 HCPV.

Marroquin Cabrera, Juan Carlos

1998-01-01T23:59:59.000Z

438

CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS  

SciTech Connect

This report describes research conducted between April 1, 2003 and June 30, 2003 on the use of dry regenerable sorbents for concentration of carbon dioxide from flue gas. Grade 1 sodium bicarbonate performed similarly to grade 5 sodium bicarbonate in fixed bed testing in that activity improved after the first carbonation cycle and did not decline over the course of 5 cycles. Thermogravimetric analysis indicated that sodium bicarbonate sorbents produced by calcination of sodium bicarbonate are superior to either soda ash or calcined trona. Energy requirements for regeneration of carbon dioxide sorbents (either wet or dry) is of primary importance in establishing the economic feasibility of carbon dioxide capture processes. Recent studies of liquid amine sorption processes were reviewed and found to incorporate conflicting assumptions of energy requirements. Dry sodium based processes have the potential to be less energy intensive and thus less expensive than oxygen inhibited amine based systems. For dry supported sorbents, maximizing the active fraction of the sorbent is of primary importance in developing an economically feasible process.

David A. Green; Brian S. Turk; Jeffrey W. Portzer; Raghubir P. Gupta; William J. McMichael; Ya Liang; Tyler Moore; Douglas P. Harrison

2003-08-01T23:59:59.000Z

439

CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS  

SciTech Connect

The objective of this project is to develop a simple and inexpensive process to separate CO{sub 2} as an essentially pure stream from a fossil fuel combustion system using a regenerable sorbent. The sorbents being investigated in this project are primarily alkali carbonates, and particularly sodium carbonate and potassium carbonate, which are converted to bicarbonates through reaction with carbon dioxide and water vapor. Bicarbonates are regenerated to carbonates when heated, producing a nearly pure CO{sub 2} stream after condensation of water vapor. This quarter, electrobalance tests suggested that higher temperature calcination of trona leds to reduced carbonation activity in subsequent cycles, but that calcination in dry carbon dioxide did not result in decreased activity relative to calcination in helium. Following higher temperature calcination, sodium bicarbonate (SBC) No.3 has greater activity than either coarse or fine grades of trona. Fixed bed testing of calcined SBC No.3 at 70 C confirmed that high rates of carbon dioxide absorption are possible and that the resulting product is a mixture of Wegscheider's salt and sodium carbonate. In fluidized bed testing of supported potassium carbonate, very rapid carbonation rates were observed. Activity of the support material complicated the data analysis. A milled, spherical grade of SBC appeared to be similar in attrition and abrasion characteristics to an unmilled, less regularly shaped SBC. The calcination behavior, at 107 C, for the milled and unmilled materials was also similar.

David A. Green; Brian S. Turk; Jeffrey W. Portzer; Raghubir P.Gupta; William J. McMichael; Ya Liang; Douglas P. Harrison

2002-10-01T23:59:59.000Z

440

Extraction of iron and calcium from low rank coal by supercritical carbon dioxide with entrainers  

SciTech Connect

Iron and calcium were extracted from low rank coal with supercritical carbon dioxide and methanol, ethanol, acetic acid, acetyl acetone, ethanol and acetic acid, or acetyl acetone and water entrainers at 313.2 K and 15.0 MPa. The low rank coal used in this study was Berau coal from Indonesia. The addition of methanol, ethanol, or acetic acid entrainers in supercritical carbon dioxide showed very limited effect on enhancement of the recovery rates of Fe. The recovery rates of Fe from dried coal by supercritical carbon dioxide with acetyl acetone were low however, the addition of acetyl acetone with water in supercritical carbon dioxide remarkably enhanced the recovery rates of Fe. Water seems to play an important role in extracting Fe from coal with supercritical carbon dioxide and acetyl acetone. On the other hand, the extraction rates of Ca with supercritical carbon dioxide and water, methanol, ethanol, and acetyl acetone entrainers were very low. The addition of acetic acid with or without water in supercritical carbon dioxide slightly enhanced the recovery rates of Ca. The addition of acetic acid with ethanol in supercritical carbon dioxide remarkably enhanced the recovery rates of Ca. The effect of carbon dioxide flow rate and coal particle size on the recovery rates of Fe were examined. The recovery rate of Fe increased with increasing carbon dioxide flow rate and with decreasing particle size of the low rank coal.

Iwai, Y.; Okamoto, N.; Ohta, S.; Arai, Y.; Sakanishi, K. [Kyushu University, Fukuoka (Japan). Dept. of Chemical Engineering

2007-03-15T23:59:59.000Z

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441

Multifunctional Oxides: Multifunctional Oxides: Synthesis and ...  

Science Conference Proceedings (OSTI)

Using Ultrafast Optical Spectroscopy to Explore Magneoelectric Coupling in Multiferroic Oxide Heterostructures: Y-M Sheu1; S. Trugman1; L Yan1; C-P Chuu 1; ...

442

Asphalt Oxidation Kinetics and Pavement Oxidation Modeling  

E-Print Network (OSTI)

Most paved roads in the United States are surfaced with asphalt. These asphalt pavements suffer from fatigue cracking and thermal cracking, aggravated by the oxidation and hardening of asphalt. This negative impact of asphalt oxidation on pavement performance has not been considered adequately in pavement design. Part of the reason is that the process of asphalt oxidation in pavement is not well understood. This work focused on understanding the asphalt oxidation kinetics and on developing pavement oxidation model that predicts asphalt oxidation and hardening in pavement under environmental conditions. A number of asphalts were studied in laboratory condition. Based on kinetics data, a fast-rate ? constant-rate asphalt oxidation kinetics model was developed to describe the early nonlinear fast-rate aging period and the later constant-rate period of asphalt oxidation. Furthermore, reaction kinetics parameters for the fast-rate and constant-rate reactions were empirically correlated, leading to a simplified model. And the experimental effort and time to obtain these kinetics parameters were significantly reduced. Furthermore, to investigate the mechanism of asphalt oxidation, two antioxidants were studied on their effectiveness. Asphalt oxidation was not significantly affected. It was found that evaluation of antioxidant effectiveness based on viscosity only is not reliable. The asphalt oxidation kinetics model was incorporated into the pavement oxidation model that predicts asphalt oxidation in pavement. The pavement oxidation model mimics the oxidation process of asphalt in real mixture at pavement temperatures. A new parameter, diffusion depth, defined the oxygen diffusion region in the mastic. A field calibration factor accounted for the factors not considered in the model such as the effect of small aggregate particles on oxygen diffusion. Carbonyl area and viscosity of binders recovered from field cores of three pavements in Texas were measured and were used for model calibration and validation. Results demonstrated that the proposed model estimates carbonyl growth over time in pavement, layer-by-layer, quite well. Finally, this work can be useful for incorporating asphalt oxidation into a pavement design method that can predict pavement performance with time and for making strategic decisions such as optimal time for maintenance treatments.

Jin, Xin

2012-05-01T23:59:59.000Z

443

SPONTANEOUS CATALYTIC WET AIR OXIDATION DURING PRE-TREATMENT OF HIGH-LEVEL RADIOACTIVE WASTE SLUDGE  

DOE Green Energy (OSTI)

Savannah River Remediation, LLC (SRR) operates the Defense Waste Processing Facility for the U.S. Department of Energy at the Savannah River Site. This facility immobilizes high-level radioactive waste through vitrification following chemical pretreatment. Catalytic destruction of formate and oxalate ions to carbon dioxide has been observed during qualification testing of non-radioactive analog systems. Carbon dioxide production greatly exceeded hydrogen production, indicating the occurrence of a process other than the catalytic decomposition of formic acid. Statistical modeling was used to relate the new reaction chemistry to partial catalytic wet air oxidation of both formate and oxalate ions driven by the low concentrations of palladium, rhodium, and/or ruthenium in the waste. Variations in process conditions led to increases or decreases in the total oxidative destruction, as well as partially shifting the preferred species undergoing destruction from oxalate ion to formate ion.

Koopman, D.; Herman, C.; Pareizs, J.; Bannochie, C.; Best, D.; Bibler, N.; Fellinger, T.

2009-10-01T23:59:59.000Z

444

Appendix B: CArBon dioxide CApture teChnology SheetS Oxygen PrOductiOn  

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

Oxygen PrOductiOn Oxygen PrOductiOn B-500 Oxygen PrOductiOn u.S. dePartment Of energy advanced carbOn diOxide caPture r&d PrOgram: technOlOgy uPdate, may 2013 itm Oxygen technOlOgy fOr integratiOn in igcc and Other advanced POwer generatiOn SyStemS primary project goals Air Products and Chemicals set out to design and develop an ion transport membrane (ITM) based on ceramics that selectively transport oxygen (O 2 ) ions when operated at high temperature. This high-temperature process may be integrated with advanced power genera- tion processes that require O 2 as a feedstock, such as integrated gasification combined cycle (IGCC) and other clean energy and industrial applications. technical goals * Design, construct, and operate a 0.1-ton/day (TPD) technology development unit

445

High-precision molecular dynamics simulation of UO2-PuO2: superionic transition in uranium dioxide  

E-Print Network (OSTI)

Our series of articles is devoted to high-precision molecular dynamics simulation of mixed actinide-oxide (MOX) fuel in the rigid ions approximation using high-performance graphics processors (GPU). In this article we assess the 10 most relevant interatomic sets of pair potential (SPP) by reproduction of the Bredig superionic phase transition (anion sublattice premelting) in uranium dioxide. The measurements carried out in a wide temperature range from 300K up to melting point with 1K accuracy allowed reliable detection of this phase transition with each SPP. The {\\lambda}-peaks obtained are smoother and wider than it was assumed previously. In addition, for the first time a pressure dependence of the {\\lambda}-peak characteristics was measured, in a range from -5 GPa to 5 GPa its amplitudes had parabolic plot and temperatures had linear (that is similar to the Clausius-Clapeyron equation for melting temperature).

Potashnikov, S I; Nekrasov, K A; Kupryazhkin, A Ya

2011-01-01T23:59:59.000Z

446

High-Temperature Co-electrolysis of Steam and Carbon Dioxide for Direct Production of Syngas; Equilibrium Model and Single-Cell Tests  

DOE Green Energy (OSTI)

An experimental study has been completed to assess the performance of single solid-oxide electrolysis cells operating over a temperature range of 800 to 850șC in the coelectrolysis mode, simultaneously electrolyzing steam and carbon dioxide for the direct production of syngas. The experiments were performed over a range of inlet flow rates of steam, carbon dioxide, hydrogen and nitrogen and over a range of current densities (-0.1 to 0.25 A/cm2) using single electrolyte-supported button electrolysis cells. Steam and carbon dioxide consumption rates associated with electrolysis were measured directly using inlet and outlet dewpoint instrumentation and a gas chromatograph, respectively. Cell operating potentials and cell current were varied using a programmable power supply. Measured values of open-cell potential and outlet gas composition are compared to predictions obtained from a chemical equilibrium coelectrolysis model. Model predictions of outlet gas composition based on an effective equilibrium temperature are shown to agree well with measurements. Cell area-specific resistance values were similar for steam electrolysis and coelectrolysis.

O'Brien, J. E.; Stoots, C. M.; Herring, J. S.; Hartvigsen, J. J.

2007-07-01T23:59:59.000Z

447

High-Temperature Co-electrolysis of Carbon Dioxide and Steam for the Production of Syngas; Equilibrium Model and Single-Cell Tests  

DOE Green Energy (OSTI)

An experimental study has been completed to assess the performance of single solid-oxide electrolysis cells operating over a temperature range of 800 to 850șC in the coelectrolysis mode, simultaneously electrolyzing steam and carbon dioxide for the direct production of syngas. The experiments were performed over a range of inlet flow rates of steam, carbon dioxide, hydrogen and nitrogen and over a range of current densities (-0.1 to 0.25 A/cm2) using single electrolyte-supported button electrolysis cells. Steam and carbon dioxide consumption rates associated with electrolysis were measured directly using inlet and outlet dewpoint instrumentation and a gas chromatograph, respectively. Cell operating potentials and cell current were varied using a programmable power supply. Measured values of open-cell potential and outlet gas composition are compared to predictions obtained from a chemical equilibrium coelectrolysis model. Model predictions of outlet gas composition based on an effective equilibrium temperature are shown to agree well with measurements. Area-specific resistance values were similar for steam electrolysis and coelectrolysis.

J. E. O'Brien; C. M. Stoots; G. L. Hawkes; J. S. Herring; J. J. Hartvigsen

2007-06-01T23:59:59.000Z

448

NIST Differential Absorption LIDAR  

Science Conference Proceedings (OSTI)

... The DIAL system is being designed to span the near infrared spectral region where the greenhouse gases, carbon dioxide, methane, and nitrous ...

2012-10-18T23:59:59.000Z

449

Determination of laser-evaporated uranium dioxide by neutron activation analysis  

SciTech Connect

Safety analyses of nuclear reactors require information about the loss of fuel which may occur at high temperatures. In this study, the surface of a uranium dioxide target was heated rapidly by a laser. The uranium surface was vaporized into a vacuum. The uranium bearing species condensed on a graphite disk placed in the pathway of the expanding uranium vapor. Scanning electron microscopy and X-ray analysis showed very little droplet ejection directly from the laser target surface. Neutron activation analysis was used to measure the amount of uranium deposited. The surface temperature was measured by a fast-response automatic optical pyrometer. The maximum surface temperature ranged from 2400 to 3700/sup 0/K. The Hertz-Langmuir formula, in conjunction with the measured surface temperature transient, was used to calculate the theoretical amount of uranium deposited. There was good agreement between theory and experiment above the melting point of 3120/sup 0/K. Below the melting point much more uranium was collected than was expected theoretically. This was attributed to oxidation of the surface. 29 refs., 16 figs., 7 tabs.

Allred, R.

1987-05-01T23:59:59.000Z

450

Mediated electrochemical oxidation of organic wastes using a Co(III) mediator in a neutral electrolyte  

DOE Patents (OSTI)

An electrochemical cell with a Co(III) mediator and neutral pH anolyte provides efficient destruction of organic and mixed wastes. The organic waste is concentrated in the anolyte reservoir, where the cobalt mediator oxidizes the organics and insoluble radioactive species and is regenerated at the anode until all organics are converted to carbon dioxide and destroyed. The neutral electrolyte is non-corrosive, and thus extends the lifetime of the cell and its components.

Balazs, G. Bryan (Livermore, CA); Lewis, Patricia R. (Livermore, CA)

1999-01-01T23:59:59.000Z

451

Mediated electrochemical oxidation of organic wastes using a Co(III) mediator in a neutral electrolyte  

DOE Patents (OSTI)

An electrochemical cell with a Co(III) mediator and neutral pH anolyte provides efficient destruction of organic and mixed wastes. The organic waste is concentrated in the anolyte reservoir, where the cobalt mediator oxidizes the organics and insoluble radioactive species and is regenerated at the anode until all organics are converted to carbon dioxide and destroyed. The neutral electrolyte is non-corrosive, and thus extends the lifetime of the cell and its components. 2 figs.

Balazs, G.B.; Lewis, P.R.

1999-07-06T23:59:59.000Z

452

EIA - Will carbon capture and storage reduce the world's carbon dioxide  

Gasoline and Diesel Fuel Update (EIA)

Will carbon capture and storage reduce the world's carbon dioxide emissions? Will carbon capture and storage reduce the world's carbon dioxide emissions? International Energy Outlook 2010 Will carbon capture and storage reduce the world'ss carbon dioxide emissions? The pursuit of greenhouse gas reductions has the potential to reduce global coal use significantly. Because coal is the most carbon-intensive of all fossil fuels, limitations on carbon dioxide emissions will raise the cost of coal relative to the costs of other fuels. Under such circumstances, the degree to which energy use shifts away from coal to other fuels will depend largely on the costs of reducing carbon dioxide emissions from coal-fired plants relative to the costs of using other, low-carbon or carbon-free energy sources. The continued widespread use of coal could rely on the cost and availability of carbon capture and storage (CCS) technologies that capture carbon dioxide and store it in geologic formations.

453

Apparatus and method for removing solvent from carbon dioxide in resin recycling system  

SciTech Connect

A two-step resin recycling system and method solvent that produces essentially contaminant-free synthetic resin material. The system and method includes one or more solvent wash vessels to expose resin particles to a solvent, the solvent contacting the resin particles in the one or more solvent wash vessels to substantially remove contaminants on the resin particles. A separator is provided to separate the solvent from the resin particles after removal from the one or more solvent wash vessels. The resin particles are next exposed to carbon dioxide in a closed loop carbon dioxide system. The closed loop system includes a carbon dioxide vessel where the carbon dioxide is exposed to the resin, substantially removing any residual solvent remaining on the resin particles after separation. A separation vessel is also provided to separate the solvent from the solvent laden carbon dioxide. Both the carbon dioxide and the solvent are reused after separation in the separation vessel.

Bohnert, George W. (Harrisonville, MO); Hand, Thomas E. (Lee's Summit, MO); DeLaurentiis, Gary M. (Jamestown, CA)

2009-01-06T23:59:59.000Z

454

Vehicle Technologies Office: Fact #479: July 23, 2007 U.S. Carbon Dioxide  

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

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455

Thermal Transport in Uranium Dioxide from First Principles  

Science Conference Proceedings (OSTI)

About this Abstract. Meeting, 2012 TMS Annual Meeting & Exhibition. Symposium , Radiation Effects in Ceramic Oxide and Novel LWR Fuels. Presentation Title ...

456

Method of determining pH by the alkaline absorption of carbon dioxide  

DOE Patents (OSTI)

A method for measuring the concentration of hydroxides in alkaline solutions in a remote location using the tendency of hydroxides to absorb carbon dioxide. The method includes the passing of carbon dioxide over the surface of an alkaline solution in a remote tank before and after measurements of the carbon dioxide solution. A comparison of the measurements yields the absorption fraction from which the hydroxide concentration can be calculated using a correlation of hydroxide or pH to absorption fraction.

Hobbs, David T. (1867 Lodgepole Ave., N. Augusta, SC 29841)

1992-01-01T23:59:59.000Z

457

The greenhouse effect and acid rain  

DOE Green Energy (OSTI)

The concentrations of carbon dioxide, methane, sulfur dioxide, nitrous oxides and chlorofluorocarbons is increasing in the earth's atmosphere. Increased concentrations of these trace gases could lead to global warming, increased acid rain and increased UV radiation on the earth's surface; however, the actual impacts are still uncertain and are also the subject of great debate. Application of clean'' energy sources such as geothermal are obviously desirable for decreasing these effects and improving our overall general environment. This paper briefly summarizes the global environment concerns, providing a backdrop for the following papers which describe the geothermal role in future environmental considerations. 5 refs., 2 figs., 1 tab.

Traeger, R.K.

1990-01-01T23:59:59.000Z

458

EIA - The National Energy Modeling System: An Overview 2003-Carbon Dioxide  

Gasoline and Diesel Fuel Update (EIA)

Carbon Dioxide and Methane Emissions Carbon Dioxide and Methane Emissions The National Energy Modeling System: An Overview 2003 Carbon Dioxide and Methane Emissions The emissions policy submodule, part of the integrating module, estimates the energy–related emissions of carbon dioxide and methane. Carbon dioxide emissions are dependent on the fossil fuel consumed, the carbon content of the fuel, and the fraction of the fuel consumed in combustion. The product of the carbon dioxide coefficient and the combustion fraction yields a carbon dioxide emission factor. For fuel uses of fossil energy, the combustion fractions are assumed to be 0.99 for liquid fuels and 0.995 for gaseous fuels. The carbon dioxide potential of nonfuel uses of energy, such as asphalt and petrochemical feedstocks, is assumed to be sequestered in the product and not released to the atmosphere. The coefficients for carbon dioxide emissions are updated each year from the Energy Information Administration’s annual, Emissions of Greenhouse Gases in the United States.17

459

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

460

Table 11.1 Carbon Dioxide Emissions From Energy Consumption by ...  

U.S. Energy Information Administration (EIA)

See Note, "Accounting for Carbon Dioxide Emissions From Biomass Energy Combustion," at end of section. 10 Wood and wood-derived fuels.

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


461

Table 11.2e Carbon Dioxide Emissions From Energy Consumption ...  

U.S. Energy Information Administration (EIA)

See Note, "Accounting for Carbon Dioxide Emissions From Biomass Energy Combustion," at end of section. R=Revised. P=Preliminary. ... 6 Wood and wood-derived fuels.

462

Table 11.2c Carbon Dioxide Emissions From Energy Consumption ...  

U.S. Energy Information Administration (EIA)

9 Wood and wood-derived fuels. 2 Carbon dioxide emissions from biomass energy consumption are excluded from total emissions in this ... non-combustion use of fossil ...

463

Table 11.2a Carbon Dioxide Emissions From Energy Consumption ...  

U.S. Energy Information Administration (EIA)

6 Wood and wood-derived fuels. ... See Note, "Accounting for Carbon Dioxide Emissions From Biomass Energy Combustion," at end of section. R=Revised. P=Preliminary.

464

Table 11.2b Carbon Dioxide Emissions From Energy Consumption ...  

U.S. Energy Information Administration (EIA)

8 Wood and wood-derived fuels. ... table. See Note, "Accounting for Carbon Dioxide Emissions From Biomass Energy Combustion," at end of section.

465

Table 11.2c Carbon Dioxide Emissions From Energy Consumption ...  

U.S. Energy Information Administration (EIA)

9 Wood and wood-derived fuels. ... table. See Note, "Accounting for Carbon Dioxide Emissions From Biomass Energy Combustion," at end of section.

466

Table 11.2e Carbon Dioxide Emissions From Energy Consumption ...  

U.S. Energy Information Administration (EIA)

Wood 6: Waste 7: Total: ... See Note, "Accounting for Carbon Dioxide Emissions From Biomass Energy Combustion," at end of section. R=Revised. P=Preliminary.

467

Table 11.1 Carbon Dioxide Emissions From Energy Consumption by ...  

U.S. Energy Information Administration (EIA)

1 Metric tons of carbon dioxide can be converted to metric tons of carbon equivalent by multiplying by 12/44. 9 Includes electric power sector use of ...

468

Table 11.2d Carbon Dioxide Emissions From Energy Consumption ...  

U.S. Energy Information Administration (EIA)

1 Metric tons of carbon dioxide can be converted to metric tons of carbon equivalent by multiplying by 12/44. 8 Fuel ethanol minus denaturant. 2 Carbo ...

469

Experimental investigation of carbon dioxide trapping due to capillary retention in deep saline aquifers.  

E-Print Network (OSTI)

??Carbon dioxide (CO2) is by far the most significant greenhouse gas released by human activities through fossil fuel combustion. In order to minimize CO2 emissions… (more)

Li, Xinqian

2013-01-01T23:59:59.000Z

470

Table 12.1 Carbon Dioxide Emissions From Energy Consumption by ...  

U.S. Energy Information Administration (EIA)

U.S. Energy Information Administration / Monthly Energy Review September 2013 159 Table 12.1 Carbon Dioxide Emissions From Energy Consumption by Source

471

Development of a Carbon Dioxide Micro Gas Sensor with Integrated AgCl Reference Electrode.  

E-Print Network (OSTI)

??ăăIn recent years, high carbon dioxide emissions not only result in serious air pollution and greenhouse effect, but also cause water acidification and decrease the… (more)

Hung, Wei-Che

2013-01-01T23:59:59.000Z

472

Synthesis and reactivity of pyridinediimine iron complexes : for the breakdown of carbon dioxide.  

E-Print Network (OSTI)

??The increase of greenhouse gases in our atmosphere, particularly carbon dioxide (CO2), has been recognized by the scientific, industrial, and political communities. The increase in… (more)

Thammavongsy, Zachary

2013-01-01T23:59:59.000Z

473

Livscykelanalys för koldioxidutsläpp frćn flerbostadshus; Life Cycle Analysis of Carbon Dioxide Emissions from Residential Buildings.  

E-Print Network (OSTI)

?? Today, about 15 to 20 percent of Sweden’s total emission of carbon dioxide can be traced to the household sector. By examining apartment blocks… (more)

Palmborg, Sofia

2013-01-01T23:59:59.000Z

474

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

475

The design, synthesis, and optimization of nanomaterials fabricated in supercritical carbon dioxide .  

E-Print Network (OSTI)

??This thesis presents investigations into the design and synthesis of nanomaterials in supercritical carbon dioxide (sc-CO?) as well as novel experimental design methodologies. First, the… (more)

Casciato, Michael John

2013-01-01T23:59:59.000Z

476

State-Level Energy-Related Carbon Dioxide Emissions, 2000-2009  

U.S. Energy Information Administration (EIA)

Overview. Energy-related carbon dioxide emissions vary significantly across states (Figure 1), whether considered on an absolute or per capita basis.

477

Sorption of Carbon Dioxide from Oxy-fuel Combustion by Lithium ...  

Science Conference Proceedings (OSTI)

Symposium, Materials for CO2 Capture and Conversion. Presentation Title, Sorption of Carbon Dioxide from Oxy-fuel Combustion by Lithium Orthosilicate.

478

A Framework for viewing theoretical, technological, economic and market potential of carbon dioxide capture and storage  

SciTech Connect

Paper presents an intelectual framework for viewing how the theoretical, technological, economic and market potentials of carbon dioxide capture and storage are related to each other.

Dooley, James J.

2004-10-04T23:59:59.000Z

479

Feasibility of Supercritical Carbon Dioxide as a Drilling Fluid for Deep Underbalanced Drilling Operations.  

E-Print Network (OSTI)

??Feasibility of drilling with supercritical carbon dioxide to serve the needs of deep underbalanced drilling operations has been analyzed. A case study involving underbalanced drilling… (more)

Gupta, Anamika

2006-01-01T23:59:59.000Z

480

Carbon Dioxide and Hydrogen Sulfide Emission Factors Applicable to Wastewater Wet Wells.  

E-Print Network (OSTI)

??Transport of wastewater in sewer networks causes potential problems associated with gases which include ammonia, carbon dioxide, carbon monoxide, hydrogen sulfide and methane, in regard… (more)

Mudragaddam, Madhuri

2010-01-01T23:59:59.000Z

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


481

Table 11.2d Carbon Dioxide Emissions From Energy Consumption ...  

U.S. Energy Information Administration (EIA)

2 Carbon dioxide emissions from biomass energy consumption are excluded from total emissions in this table. ... non-combustion use of fossil fuels.

482

Table 11.2b Carbon Dioxide Emissions From Energy Consumption ...  

U.S. Energy Information Administration (EIA)

See Note, "Accounting for Carbon Dioxide Emissions From Biomass Energy Combustion," at end of ... other biomass. 3 Natural gas, excluding supplemental gaseous fuels.

483

Table 11.2a Carbon Dioxide Emissions From Energy Consumption ...  

U.S. Energy Information Administration (EIA)

table. See Note, "Accounting for Carbon Dioxide Emissions From Biomass Energy Combustion," at end of section. R=Revised. P=Preliminary.

484

METHOD OF DISSOLVING PLUTONIUM DIOXIDE IN NITRIC ACID USING CERIUM IONS  

DOE Patents (OSTI)

A method is descnibed for catalyzing the dissolution of plutenium dioxide in nitric acid with small amounts of cerium ions. (AEC)

Wilson, A.S.

1961-10-24T23:59:59.000Z

485

S&TR | May 2005: Locked in Rock: Sequestering Carbon Dioxide...  

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

abundant greenhouse gas is carbon dioxide (CO2). Many climate research studies focus on developing technologies to greatly reduce the atmospheric levels of CO2. One approach...

486

Strained Ge channel p-type metal-oxide-semiconductor field-effect transistors grown on Siâ?â??xGex/Si virtual substrates  

E-Print Network (OSTI)

We have fabricated strained Ge channel p-type metal-oxide-semiconductor field-effect transistors (p-MOSFETs) on Siâ??.â??Geâ??.â?? virtual substrates. The poor interface between silicon dioxide (SiOâ??) and the Ge channel ...

Lee, Minjoo L.

487

NETL: Electrochemical Membranes for Carbon Dioxide Capture and Power  

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

Electrochemical Membranes for Carbon Dioxide Capture and Power Generation Electrochemical Membranes for Carbon Dioxide Capture and Power Generation Project No.: DE-FE0007634 FuelCell Energy, Inc. has developed a novel system concept for the separation of carbon dioxide (CO2) from greenhouse gas (GHG) emission sources using an electrochemical membrane. The proposed membrane has its genesis from the company's patented Direct FuelCellÂź (DFCÂź) technology. The prominent feature of the DFC membrane is its capability to produce power while capturing CO2 from the flue gas from a pulverized coal (PC) plant. The DFC membrane does not require flue gas compression as it operates on the principles of electrochemistry, resulting in net efficiency gains. The membrane utilizes a fuel (different from the plant flue gas, such as coal-derived syngas, natural gas, or a renewable resource) as the driver for the combined carbon capture and electric power generation. The electrochemical membrane consists of ceramic-based layers filled with carbonate salts, separating CO2 from the flue gas. Because of the electrode's high reaction rates, the membrane does not require a high CO2 concentration in its feed gas. The planar geometry of the membrane offers ease of scalability to large sizes suitable for deployment in PC plants, which is an important attribute in membrane design. The membrane has been tested at the laboratory scale, verifying the feasibility of the technology for CO2 separation from simulated flue gases of PC plants as well as combined cycle power plants and other industrial facilities. Fuel Cell Energy, Inc. is advancing the technology to a maturity level suitable for adaption by industry for pilot-scale demonstration and subsequent commercial deployment.

488

Household carbon dioxide production in relation to the greenhouse effect  

SciTech Connect

A survey of 655 households from eastern suburbs of Melbourne was undertaken to determine householders[prime] attitudes to, and understanding of, the greenhouse effect. Carbon dioxide emissions resulting from car, electricity and gas use were computed and household actions which could reduce CO[sub 2] emissions were addressed. Preliminary analysis of the results indicates that householders in this area are aware of, and concerned about, the greenhouse effect, although their understanding of its causes is often poor. Many appreciate the contribution of cars, but are unclear about the relative importance of other household activities. Carbon dioxide emissions from the three sources examined averaged 21[center dot]2 tonnes/year per household and 7[center dot]4 tonnes/year per person. Electricity was the largest contributor (8[center dot]6 tonnes/year), cars the next largest (7[center dot]7 tonnes/year) and gas third (5[center dot] tonnes/year) per household. Emissions varied considerably from household to household. There was a strong positive correlation between availability of economic resources and household CO[sub 2] output from all sources. Carbon dioxide production, particularly from car use, was greater from households which were most distant from a railway station, and from larger households, and numbers of children in the household had little effect on emissions. There were also some economics of scale for households containing more adults. Understanding the causes of the greenhouse bore little relation to change in CO[sub 2] emissions; being concerned about it was associated with a small reduction; but actual actions to reduce car use and household heating, however motivated, produced significant reductions. 12 refs., 9 figs., 6 tabs.

Stokes, D.; Lindsay, A.; Marinopoulos, J.; Treloar, A.; Wescott, G. (Deakin Univ., Clayton (Australia))

1994-03-01T23:59:59.000Z

489

CARBON DIOXIDE CAPTURE FROM FLUE GAS USING DRY REGENERABLE SORBENTS  

SciTech Connect

The objective of this project is to develop a simple, inexpensive process to separate CO{sub 2} as an essentially pure stream from a fossil fuel combustion system using a regenerable, sodium-based sorbent. The sorbents being investigated in this project are primarily alkali carbonates, and particularly sodium carbonate and potassium carbonate, which are converted to bicarbonates, through reaction with carbon dioxide and water vapor. Bicarbonates are regenerated to carbonates when heated, producing a nearly pure CO{sub 2} stream after condensation of water vapor. This quarter, electrobalance tests conducted at LSU indicated that exposure of sorbent to water vapor prior to contact with carbonation gas does not significantly increase the reaction rate. Calcined fine mesh trona has a greater initial carbonation rate than calcined sodium bicarbonate, but appears to be more susceptible to loss of reactivity under severe calcination conditions. The Davison attrition indices for Grade 5 sodium bicarbonate, commercial grade sodium carbonate and extra fine granular potassium carbonate were, as tested, outside of the range suitable for entrained bed reactor testing. Fluidized bed testing at RTI indicated that in the initial stages of reaction potassium carbonate removed 35% of the carbon dioxide in simulated flue gas, and is reactive at higher temperatures than sodium carbonate. Removals declined to 6% when 54% of the capacity of the sorbent was exhausted. Carbonation data from electrobalance testing was correlated using a shrinking core reaction model. The activation energy of the reaction of sodium carbonate with carbon dioxide and water vapor was determined from nonisothermal thermogravimetry.

David A. Green; Brian S. Turk; Raghubir P. Gupta; William J. McMichael; Douglas P. Harrison; Ya Liang

2002-04-01T23:59:59.000Z

490

Development studies for a novel wet oxidation process  

SciTech Connect

A catalytic wet oxidation process (DETOX), which uses an acidic iron solution to oxidize organic compounds to carbon dioxide, water, and other simple products, was investigated as a potential method for the treatment of multicomponent hazardous and mixed wastes. The organic compounds picric acid, poly(vinyl chloride), tetrachlorothiophene, pentachloropyridine, Aroclor 1260 (a polychlorinated biphenyl), and hexachlorobenzene were oxidized in 125 ml reaction vessels. The metals arsenic, barium, beryllium, cadmium, cerium (as a surrogate for plutonium), chromium, lead, mercury, neodymium (as a surrogate for uranium), nickel, and vanadium were tested in the DETOX solution. Barium, beryllium, cerium, chromium, mercury, neodymium, nickel, and vanadium were all found to be very soluble (>100 g/l) in the DETOX chloride-based solution. Arsenic, barium, cadmium, and lead solubilities were lower. Lead could be selectively precipitated from the DETOX solution. Chromium(VI) was reduced to relatively non-toxic chromium(III) by the solution. Six soils were contaminated with arsenic, barium, beryllium, chromium, lead, and neodymium oxides at approximately 0.1% by weight, and benzene, trichloroethene, mineral oil, and Aroclor 1260 at approximately 5% by weight total, and 5.g amounts treated with the DETOX solution in unstirred 125. ml reaction bombs. It is felt that soil treatment in a properly designed system is entirely possible despite incomplete oxidation of the less volatile organic materials in these unstirred tests.

Dhooge, P.M.; Hakim, L.B.

1994-01-01T23:59:59.000Z

491

CATALYST EVALUATION FOR A SULFUR DIOXIDE-DEPOLARIZED ELECTROLYZER  

DOE Green Energy (OSTI)

Thermochemical processes are being developed to provide global-scale quantities of hydrogen. A variant on sulfur-based thermochemical cycles is the Hybrid Sulfur (HyS) Process which uses a sulfur dioxide depolarized electrolyzer (SDE) to produce the hydrogen. Testing examined the activity and stability of platinum and palladium as the electrocatalyst for the SDE in sulfuric acid solutions. Cyclic and linear sweep voltammetry revealed that platinum provided better catalytic activity with much lower potentials and higher currents than palladium. Testing also showed that the catalyst activity is strongly influenced by the concentration of the sulfuric acid electrolyte.

Hobbs, D; Hector Colon-Mercado, H

2007-01-31T23:59:59.000Z

492

A Sensor System Based on Semi-Conductor Metal Oxide Technology for In Situ Detection of Coal Fired Combustion Gases  

SciTech Connect

Sensor Research and Development Corporation (SRD) proposed a two-phase program to develop a robust, autonomous prototype analyzer for in situ, real-time detection, identification, and measurement of coal-fired combustion gases and perform field-testing at an approved power generation facility. SRD developed and selected sensor materials showing selective responses to carbon monoxide, carbon dioxide, nitric oxide, nitrogen dioxide, ammonia, sulfur dioxide and hydrogen chloride. Sensor support electronics were also developed to enable prototype to function in elevated temperatures without any issues. Field-testing at DOE approved facility showed the ability of the prototype to detect and estimate the concentration of combustion by-products accurately with relatively low false-alarm rates at very fast sampling intervals.

Brent Marquis

2007-05-31T23:59:59.000Z

493

Summary report : direct approaches for recycling carbon dioxide into synthetic fuel.  

DOE Green Energy (OSTI)

The consumption of petroleum by the transportation sector in the United States is roughly equivalent to petroleum imports into the country, which have totaled over 12 million barrels a day every year since 2004. This reliance on foreign oil is a strategic vulnerability for the economy and national security. Further, the effect of unmitigated CO{sub 2} releases on the global climate is a growing concern both here and abroad. Independence from problematic oil producers can be achieved to a great degree through the utilization of non-conventional hydrocarbon resources such as coal, oil-shale and tarsands. However, tapping into and converting these resources into liquid fuels exacerbates green house gas (GHG) emissions as they are carbon rich, but hydrogen deficient. Revolutionary thinking about energy and fuels must be adopted. We must recognize that hydrocarbon fuels are ideal energy carriers, but not primary energy sources. The energy stored in a chemical fuel is released for utilization by oxidation. In the case of hydrogen fuel the chemical product is water; in the case of a hydrocarbon fuel, water and carbon dioxide are produced. The hydrogen economy envisions a cycle in which H{sub 2}O is re-energized by splitting water into H{sub 2} and O{sub 2}, by electrolysis for example. We envision a hydrocarbon analogy in which both carbon dioxide and water are re-energized through the application of a persistent energy source (e.g. solar or nuclear). This is of course essentially what the process of photosynthesis accomplishes, albeit with a relatively low sunlight-to-hydrocarbon efficiency. The goal of this project then was the creation of a direct and efficient process for the solar or nuclear driven thermochemical conversion of CO{sub 2} to CO (and O{sub 2}), one of the basic building blocks of synthetic fuels. This process would potentially provide the basis for an alternate hydrocarbon economy that is carbon neutral, provides a pathway to energy independence, and is compatible with much of the existing fuel infrastructure.

Allendorf, Mark D. (Sandia National Laboratories, Livermore, CA); Ambrosini, Andrea; Diver, Richard B., Jr.; Siegel, Nathan Phillip; Miller, James Edward; Gelbard, Fred; Evans, Lindsey R.

2009-01-01T23:59:59.000Z

494

Device for staged carbon monoxide oxidation  

DOE Patents (OSTI)

A method and apparatus for selectively oxidizing carbon monoxide in a hydrogen rich feed stream. The method comprises mixing a feed stream consisting essentially of hydrogen, carbon dioxide, water and carbon monoxide with a first predetermined quantity of oxygen (air). The temperature of the mixed feed/oxygen stream is adjusted in a first the heat exchanger assembly (20) to a first temperature. The mixed feed/oxygen stream is sent to reaction chambers (30,32) having an oxidation catalyst contained therein. The carbon monoxide of the feed stream preferentially absorbs on the catalyst at the first temperature to react with the oxygen in the chambers (30,32) with minimal simultaneous reaction of the hydrogen to form an intermediate hydrogen rich process stream having a lower carbon monoxide content than the feed stream. The elevated outlet temperature of the process stream is carefully controlled in a second heat exchanger assembly (42) to a second temperature above the first temperature. The process stream is then mixed with a second predetermined quantity of oxygen (air). The carbon monoxide of the process stream preferentially reacts with the second quantity of oxygen in a second stage reaction chamber (56) with minimal simultaneous reaction of the hydrogen in the process stream. The reaction produces a hydrogen rich product stream having a lower carbon monoxide content than the process stream. The product stream is then cooled in a third heat exchanger assembly (72) to a third predetermined temperature. Three or more stages may be desirable, each with metered oxygen injection.

Vanderborgh, Nicholas E. (Los Alamos, NM); Nguyen, Trung V. (College Station, TX); Guante, Jr., Joseph (Denver, CO)

1993-01-01T23:59:59.000Z

495

Partial oxidation catalyst  

DOE Patents (OSTI)

A two-part catalyst comprising a dehydrogenation portion and an oxide-ion conducting portion. The dehydrogenation portion is a group VIII metal and the oxide-ion conducting portion is selected from a ceramic oxide crystallizing in the fluorite or perovskite structure. There is also disclosed a method of forming a hydrogen rich gas from a source of hydrocarbon fuel in which the hydrocarbon fuel contacts a two-part catalyst comprising a dehydrogenation portion and an oxide-ion conducting portion at a temperature not less than about 400.degree. C. for a time sufficient to generate the hydrogen rich gas while maintaining CO content less than about 5 volume percent. There is also disclosed a method of forming partially oxidized hydrocarbons from ethanes in which ethane gas contacts a two-part catalyst comprising a dehydrogenation portion and an oxide-ion conducting portion for a time and at a temperature sufficient to form an oxide.

Krumpelt, Michael (Naperville, IL); Ahmed, Shabbir (Bolingbrook, IL); Kumar, Romesh (Naperville, IL); Doshi, Rajiv (Downers Grove, IL)

2000-01-01T23:59:59.000Z

496

Quantitative room-temperature mineralization of airborne formaldehyde using manganese oxide catalysts  

E-Print Network (OSTI)

extent of mineralization Carbon dioxide levels produced as athe formation of carbon dioxide and water. The concentrationformaldehyde and carbon dioxide concentrations were recorded

Sidheswaran, Meera A.

2012-01-01T23:59:59.000Z

497

Electro-catalytic oxidation device for removing carbon from a fuel reformate  

SciTech Connect

An electro-catalytic oxidation device (ECOD) for the removal of contaminates, preferably carbonaceous materials, from an influent comprising an ECOD anode, an ECOD cathode, and an ECOD electrolyte. The ECOD anode is at a temperature whereby the contaminate collects on the surface of the ECOD anode as a buildup. The ECOD anode is electrically connected to the ECOD cathode, which consumes the buildup producing electricity and carbon dioxide. The ECOD anode is porous and chemically active to the electro-catalytic oxidation of the contaminate. The ECOD cathode is exposed to oxygen, and made of a material which promotes the electro-chemical reduction of oxygen to oxidized ions. The ECOD electrolyte is non-permeable to gas, electrically insulating and a conductor to oxidized. The ECOD anode is connected to the fuel reformer and the fuel cell. The ECOD electrolyte is between and in ionic contact with the ECOD anode and the ECOD cathode.

Liu, Di-Jia (Naperville, IL)

2010-02-23T23:59:59.000Z

498

Process and apparatus for generating elemental sulfur and re-usable metal oxide from spent metal sulfide sorbents  

DOE Patents (OSTI)

A process and apparatus for generating elemental sulfur and re-usable metal oxide from spent metal-sulfur compound. Spent metal-sulfur compound is regenerated to re-usable metal oxide by moving a bed of spent metal-sulfur compound progressively through a single regeneration vessel having a first and second regeneration stage and a third cooling and purging stage. The regeneration is carried out and elemental sulfur is generated in the first stage by introducing a first gas of sulfur dioxide which contains oxygen at a concentration less than the stoichiometric amount required for complete oxidation of the spent metal-sulfur compound. A second gas containing sulfur dioxide and excess oxygen at a concentration sufficient for complete oxidation of the partially spent metal-sulfur compound, is introduced into the second regeneration stage. Gaseous sulfur formed in the first regeneration stage is removed prior to introducing the second gas into the second regeneration stage. An oxygen-containing gas is introduced into the third cooling and purging stage. Except for the gaseous sulfur removed from the first stage, the combined gases derived from the regeneration stages which are generally rich in sulfur dioxide and lean in oxygen, are removed from the regenerator as an off-gas and recycled as the first and second gas into the regenerator. Oxygen concentration is controlled by adding air, oxygen-enriched air or pure oxygen to the recycled off-gas.

Ayala, Raul E. (Clifton Park, NY); Gal, Eli (Lititz, PA)

1995-01-01T23:59:59.000Z

499

Table 22. Total Carbon Dioxide Emissions, Projected vs. Actual  

Gasoline and Diesel Fuel Update (EIA)

Total Carbon Dioxide Emissions, Projected vs. Actual Total Carbon Dioxide Emissions, Projected vs. Actual (million metric tons) 1985 1986 1987 1988 1989 1990 1991 1992 1993 1994 1995 1996 1997 1998 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008 2009 AEO 1982 AEO 1983 AEO 1984 AEO 1985 AEO 1986 AEO 1987 AEO 1989* AEO 1990 AEO 1991 AEO 1992 AEO 1993 5009 5053 5130 5207 5269 5335 5401 5449 5504 5562 5621 5672 5724 5771 5819 5867 5918 5969 AEO 1994 5060 5130 5185 5240 5287 5335 5379 5438 5482 5529 5599 5658 5694 5738 5797 5874 5925 AEO 1995 5137 5174 5188 5262 5309 5361 5394 5441.3 5489.0 5551.3 5621.0 5679.7 5727.3 5775.0 5841.0 5888.7 AEO 1996 5182 5224 5295 5355 5417 5464 5525 5589 5660 5735 5812 5879 5925 5981 6030 AEO 1997 5295 5381 5491 5586 5658 5715 5781 5863 5934 6009 6106 6184 6236 6268 AEO 1998 5474 5621 5711 5784 5893 5957 6026 6098 6192 6292 6379 6465 6542 AEO 1999 5522 5689 5810 5913 5976 6036 6084 6152 6244 6325 6418 6493 AEO 2000

500

Carbon Dioxide Information Analysis Center: FY 1991 activities  

SciTech Connect

During the course of a fiscal year, Oak Ridge National Laboratory`s Carbon Dioxide Information Analysis Center (CDIAC) distributes thousands of specially publications-numeric data packages (NDPs), computer model packages (CMPs), technical reports, public communication publications, newsletters, article reprints, and reference boo