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Note: This page contains sample records for the topic "reduce sulfur dioxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
they are not comprehensive nor are they the most current set.
We encourage you to perform a real-time search of NLEBeta
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1

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,

2

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

3

Sulfide catalysts for reducing SO2 to elemental sulfur  

DOE Patents (OSTI)

A highly efficient sulfide catalyst for reducing sulfur dioxide to elemental sulfur, which maximizes the selectivity of elemental sulfur over byproducts and has a high conversion efficiency. Various feed stream contaminants, such as water vapor are well tolerated. Additionally, hydrogen, carbon monoxide, or hydrogen sulfides can be employed as the reducing gases while maintaining high conversion efficiency. This allows a much wider range of uses and higher level of feed stream contaminants than prior art catalysts.

Jin, Yun (Peking, CN); Yu, Qiquan (Peking, CN); Chang, Shih-Ger (El Cerrito, CA)

2001-01-01T23:59:59.000Z

4

Sulfur dioxide and nitrogen dioxide levels inside and outside homes and the implications on health effects research  

Science Journals Connector (OSTI)

Sulfur dioxide and nitrogen dioxide levels inside and outside homes and the implications on health effects research ...

John D. Spengler; Benjamin G. Ferris Jr.; Douglas W. Dockery; Frank E. Speizer

1979-10-01T23:59:59.000Z

5

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

6

Advanced Byproduct Recovery: Direct Catalytic Reduction of Sulfur Dioxide to Elemental Sulfur.  

SciTech Connect

More than 170 wet scrubber systems applied, to 72,000 MW of U.S., coal-fired, utility boilers are in operation or under construction. In these systems, the sulfur dioxide removed from the boiler flue gas is permanently bound to a sorbent material, such as lime or limestone. The sulfated sorbent must be disposed of as a waste product or, in some cases, sold as a byproduct (e.g. gypsum). Due to the abundance and low cost of naturally occurring gypsum, and the costs associated with producing an industrial quality product, less than 7% of these scrubbers are configured to produce usable gypsum (and only 1% of all units actually sell the byproduct). The disposal of solid waste from each of these scrubbers requires a landfill area of approximately 200 to 400 acres. In the U.S., a total of 19 million tons of disposable FGD byproduct are produced, transported and disposed of in landfills annually. The use of regenerable sorbent technologies has the potential to reduce or eliminate solid waste production, transportation and disposal. In a regenerable sorbent system, the sulfur dioxide in the boiler flue gas is removed by the sorbent in an adsorber. The S0{sub 2}s subsequently released, in higher concentration, in a regenerator. All regenerable systems produce an off-gas stream from the regenerator that must be processed further in order to obtain a salable byproduct, such as elemental sulfur, sulfuric acid or liquid S0{sub 2}.

NONE

1997-06-01T23:59:59.000Z

7

Reducing carbon dioxide to products  

DOE Patents (OSTI)

A method reducing carbon dioxide to one or more products may include steps (A) to (C). Step (A) may bubble said carbon dioxide into a solution of an electrolyte and a catalyst in a divided electrochemical cell. The divided electrochemical cell may include an anode in a first cell compartment and a cathode in a second cell compartment. The cathode may reduce said carbon dioxide into said products. Step (B) may adjust one or more of (a) a cathode material, (b) a surface morphology of said cathode, (c) said electrolyte, (d) a manner in which said carbon dioxide is bubbled, (e), a pH level of said solution, and (f) an electrical potential of said divided electrochemical cell, to vary at least one of (i) which of said products is produced and (ii) a faradaic yield of said products. Step (C) may separate said products from said solution.

Cole, Emily Barton; Sivasankar, Narayanappa; Parajuli, Rishi; Keets, Kate A

2014-09-30T23:59:59.000Z

8

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

9

CATALYST EVALUATION FOR A SULFUR DIOXIDE-DEPOLARIZED ELECTROLYZER  

SciTech Connect

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

10

Advanced byproduct recovery: Direct catalytic reduction of sulfur dioxide to elemental sulfur. Fourth quarterly technical progress report  

SciTech Connect

The team of Arthur D. Little, Tufts University and Engelhard Corporation are conducting Phase 1 of a four and a half year, two-phase effort to develop and scale-up an advanced byproduct recovery technology that is a direct, single-stage, catalytic process for converting sulfur dioxide to elemental sulfur. This catalytic process reduces SO{sub 2} over a fluorite-type oxide (such as ceria and zirconia). The catalytic activity can be significantly promoted by active transition metals, such as copper. More than 95% elemental sulfur yield, corresponding to almost complete sulfur dioxide conversion, was obtained over a Cu-Ce-O oxide catalyst as part of an on-going DOE-sponsored, University Coal Research Program. This type of mixed metal oxide catalyst has stable activity, high selectivity for sulfur production, and is resistant to water and carbon dioxide poisoning. Tests with CO and CH{sub 4} reducing gases indicate that the catalyst has the potential for flexibility with regard to the composition of the reducing gas, making it attractive for utility use. The performance of the catalyst is consistently good over a range of SO{sub 2} inlet concentration (0.1 to 10%) indicating its flexibility in treating SO{sub 2} tail gases as well as high concentration streams.

NONE

1997-01-01T23:59:59.000Z

11

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

12

Advanced byproduct recovery: Direct catalytic reduction of sulfur dioxide to elemental sulfur. Quarterly report, April 1--June 30, 1997  

SciTech Connect

The team of Arthur D. Little, Tufts University and Engelhard Corporation are conducting Phase 1 of a four and a half year, two-phase effort to develop and scale-up an advanced byproduct recovery technology that is a direct, single-stage, catalytic process for converting sulfur dioxide to elemental sulfur. This catalytic process reduces SO{sub 2} over a fluorite-type oxide (such as ceria and zirconia). The catalytic activity can be significantly promoted by active transition metals, such as copper. More than 95% elemental sulfur yield, corresponding to almost complete sulfur dioxide conversion, was obtained over a Cu-Ce-O oxide catalyst as part of an on-going DOE-sponsored, University Coal Research Program. This type of mixed metal oxide catalyst has stable activity, high selectivity for sulfur production, and is resistant to water and carbon dioxide poisoning. Tests with CO and CH{sub 4} reducing gases indicate that the catalyst has the potential for flexibility with regard to the composition of the reducing gas, making it attractive for utility use. The performance of the catalyst is consistently good over a range of SO{sub 2} inlet concentration (0.1 to 10%) indicating its flexibility in treating SO{sub 2} tail gases as well as high concentration streams. The principal objective of the Phase 1 program is to identify and evaluate the performance of a catalyst which is robust and flexible with regard to choice of reducing gas. In order to achieve this goal, the authors have planned a structured program including: Market/process/cost/evaluation; Lab-scale catalyst preparation/optimization studies; Lab-scale, bulk/supported catalyst kinetic studies; Bench-scale catalyst/process studies; and Utility review. Progress is reported from all three organizations.

NONE

1997-12-31T23:59:59.000Z

13

Auction design and the market for sulfur dioxide emissions  

E-Print Network (OSTI)

Title IV of the Clean Air Act Amendments of 1990 created a market for electric utility emissions of sulfur dioxide (SO2). Recent papers have argued that flaws in the design of the auctions that are part of this market have ...

Joskow, Paul L.

1996-01-01T23:59:59.000Z

14

Historical Sulfur Dioxide Emissions 1850-2000: Methods and Results  

SciTech Connect

A global, self-consistent estimate of sulfur dioxide emissions over the last one and a half century were estimated by using a combination of bottom-up and best available inventory methods including all anthropogenic sources. We find that global sulfur dioxide emissions peaked about 1980 and have generally declined since this time. Emissions were extrapolated to a 1{sup o} x 1{sup o} grid for the time period 1850-2000 at annual resolution with two emission height levels and by season. Emissions are somewhat higher in the recent past in this new work as compared with some comprehensive estimates. This difference is largely due to our use of emissions factors that vary with time to account for sulfur removals from fossil fuels and industrial smelting processes.

Smith, Steven J.; Andres, Robert; Conception , Elvira; Lurz, Joshua

2004-01-25T23:59:59.000Z

15

Advanced product recovery: Direct catalytic reduction of sulfur dioxide to elemental sulfur. Third quarterly technical progress report  

SciTech Connect

More than 170 wet scrubber systems applied to 72,000 MW of US, coal-fired, utility boilers are in operation or under construction. In these systems, the sulfur dioxide removed form the boiler flue gas is permanently bound to a sorbent material, such as lime or limestone. The sulfated sorbent must be disposed of as a waste product or, in some cases, sold as a byproduct (e.g. gypsum). The use of regenerable sorbent technologies has the potential to reduce or eliminate solid waste production, transportation and disposal. Arthur D. Little, Inc., together with its industry and commercialization advisor, Engelhard Corporation, and its university partner, Tufts, plans to develop and scale-up an advanced, byproduct recovery technology that is a direct, catalytic process for reducing sulfur dioxide to elemental sulfur. The principal objective of the Phase 1 program is to identify and evaluate the performance of a catalyst which is robust and flexible with regard to choice of reducing gas. In order to achieve this goal, they have planned a structured program including: market/process/cost/evaluation; lab-scale catalyst preparation/optimization studies; lab-scale, bulk/supported catalyst kinetic studies; bench-scale catalyst/process studies; and utility review. This catalytic process reduces SO{sub 2} over a fluorite-type oxide (such as ceria and zirconia). The catalytic activity can be significantly promoted by active transition metals, such as copper. This type of mixed metal oxide catalyst has stable activity, high selectivity for sulfur production, and is resistant to water and carbon dioxide poisoning.

NONE

1996-07-01T23:59:59.000Z

16

Advanced Byproduct Recovery: Direct Catalytic Reduction of Sulfur Dioxide to Elemental Sulfur. Fifth quarterly technical progress report, December 1996  

SciTech Connect

More than 170 wet scrubber systems applied, to 72,000 MW of U.S., coal-fired, utility boilers are in operation or under construction. In these systems, the sulfur dioxide removed from the boiler flue gas is permanently bound to a sorbent material, such as lime or limestone. The sulfated sorbent must be disposed of as a waste product or, in some cases, sold as a byproduct (e.g. gypsum). Due to the abundance and low cost of naturally occurring gypsum, and the costs associated with producing an industrial quality product, less than 7% of these scrubbers are configured to produce usable gypsum (and only 1% of all units actually sell the byproduct). The disposal of solid waste from each of these scrubbers requires a landfill area of approximately 200 to 400 acres. In the U.S., a total of 19 million tons of disposable FGD byproduct are produced, transported and disposed of in landfills annually. The use of regenerable sorbent technologies has the potential to reduce or eliminate solid waste production, transportation and disposal. In a regenerable sorbent system, the sulfur dioxide in the boiler flue gas is removed by the sorbent in an adsorber. The S0{sub 2}s subsequently released, in higher concentration, in a regenerator. All regenerable systems produce an off-gas stream from the regenerator that must be processed further in order to obtain a salable byproduct, such as elemental sulfur, sulfuric acid or liquid S0{sub 2}.

NONE

1996-12-01T23:59:59.000Z

17

Advanced Byproduct Recovery: Direct Catalytic Reduction of Sulfur Dioxide to Elemental Sulfur. Sixth quarterly technical progress report, January - March 1997  

SciTech Connect

More than 170 wet scrubber systems applied, to 72,000 MW of U.S., coal-fired, utility boilers are in operation or under construction. In these systems, the sulfur dioxide removed from the boiler flue gas is permanently bound to a sorbent material, such as lime or limestone. The sulfated sorbent must be disposed of as a waste product or, in some cases, sold as a byproduct (e.g. gypsum). Due to the abundance and low cost of naturally occurring gypsum, and the costs associated with producing an industrial quality product, less than 7% of these scrubbers are configured to produce usable gypsum (and only 1% of all units actually sell the byproduct). The disposal of solid waste from each of these scrubbers requires a landfill area of approximately 200 to 400 acres. In the U.S., a total of 19 million tons of disposable FGD byproduct are produced, transported and disposed of in landfills annually. The use of regenerable sorbent technologies has the potential to reduce or eliminate solid waste production, transportation and disposal. In a regenerable sorbent system, the sulfur dioxide in the boiler flue gas is removed by the sorbent in an adsorber. The S0{sub 2}s subsequently released, in higher concentration, in a regenerator. All regenerable systems produce an off-gas stream from the regenerator that must be processed further in order to obtain a salable byproduct, such as elemental sulfur, sulfuric acid or liquid S0{sub 2}.

NONE

1997-03-01T23:59:59.000Z

18

SYNTHESIS OF SULFUR-BASED WATER TREATMENT AGENT FROM SULFUR DIOXIDE WASTE STREAMS  

SciTech Connect

We propose a process that uses sulfur dioxide from coal combustion as a raw material to synthesize polymeric ferric sulfate (PFS), a water treatment agent. The process uses sodium chlorate as an oxidant and ferrous sulfate as an absorbent. The major chemical mechanisms in this reaction system include oxidation, hydrolysis, and polymerization. Oxidation determines sulfur conversion efficiency while hydrolysis and polymerization control the quality of product. Many factors, including SO{sub 2} inlet concentration, flow rate of simulated flue gas, reaction temperature, addition rate of oxidant and stirring rate, may affect the efficiencies of SO{sub 2} removal. Currently, the effects of SO{sub 2} inlet concentration, the flow rate of simulated flue gas and addition rate of flue gas on removal efficiencies of SO{sub 2}, are being investigated. Experiments shown in this report have demonstrated that the conversion efficiencies of sulfur dioxide with ferrous sulfate as an absorbent are in the range of 60-80% under the adopted process conditions. However, the conversion efficiency of sulfur dioxide may be improved by optimizing reaction conditions to be investigated. Partial quality indices of the synthesized products, including Fe{sup 2+} concentration and total iron concentration, have been evaluated.

Robert C. Brown; Maohong Fan

2001-12-01T23:59:59.000Z

19

E-Print Network 3.0 - absorbing sulfur dioxide Sample Search...  

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

provides some chemicals which are incompatible with other compounds. Summary: Potassium carbon tetrachloride, carbon dioxide, water Potassium chlorate sulfuric and other acids...

20

E-Print Network 3.0 - ambient sulfur dioxide Sample Search Results  

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

provides some chemicals which are incompatible with other compounds. Summary: Potassium carbon tetrachloride, carbon dioxide, water Potassium chlorate sulfuric and other acids...

Note: This page contains sample records for the topic "reduce sulfur dioxide" 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

Instrument Development and Measurements of the Atmospheric Pollutants Sulfur Dioxide, Nitrate Radical, and Nitrous Acid by Cavity Ring-down Spectroscopy and Cavity Enhanced Absorption Spectroscopy  

E-Print Network (OSTI)

A. , A method of nitrogen dioxide and sulphur dioxidedetermination of nitrogen dioxide and sulfur dioxide in theDOAS) have measured nitrogen dioxide (NO 2 ), nitrate

Medina, David Salvador

2011-01-01T23:59:59.000Z

22

Effects of Sulfur Dioxide on Formation of Fishy Off-Odor and Undesirable Taste in Wine Consumed with Seafood  

Science Journals Connector (OSTI)

Effects of Sulfur Dioxide on Formation of Fishy Off-Odor and Undesirable Taste in Wine Consumed with Seafood ... These results suggest that sulfur dioxide in wine participated in degradation of unsaturated fatty acids, causing an increase in undesirable taste and fishy off-odor in wine and seafood pairings. ... Wine; seafood; fishy off-odor; undesirable taste; unsaturated fatty acids; sulfur dioxide ...

Akiko Fujita; Atsuko Isogai; Michiko Endo; Hitoshi Utsunomiya; Shigeyoshi Nakano; Hiroshi Iwata

2010-03-10T23:59:59.000Z

23

Physicochemical aspects of the adsorption of sulfur dioxide by carbon adsorbents  

Science Journals Connector (OSTI)

Literature data on the chemistry of the adsorption of sulfur dioxide on carbon adsorbents are surveyed and described systematically. The influence of various factors (the nature of the carbon matrix, the activation method, the chemistry of the adsorbent surfaces, temperature, the composition of the gas stream, etc.) on the sorption of SO2 by activated carbons and semicokes is examined. The possible ways in which sulfur dioxide interacts with the carbon surface are discussed. The bibliography includes 128 references.

Sergey A Anurov

1996-01-01T23:59:59.000Z

24

Process for production of synthesis gas with reduced sulfur content  

DOE Patents (OSTI)

A process for the partial oxidation of a sulfur- and silicate-containing carbonaceous fuel to produce a synthesis gas with reduced sulfur content which comprises partially oxidizing said fuel at a temperature in the range of 1800.degree.-2200.degree. F. in the presence of a temperature moderator, an oxygen-containing gas and a sulfur capture additive which comprises an iron-containing compound portion and a sodium-containing compound portion to produce a synthesis gas comprising H.sub.2 and CO with a reduced sulfur content and a molten slag which comprises (i) a sulfur-containing sodium-iron silicate phase and (ii) a sodium-iron sulfide phase. The sulfur capture additive may optionally comprise a copper-containing compound portion.

Najjar, Mitri S. (Hopewell Junction, NY); Corbeels, Roger J. (Wappingers Falls, NY); Kokturk, Uygur (Wappingers Falls, NY)

1989-01-01T23:59:59.000Z

25

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

E-Print Network (OSTI)

world-best-practice-energy- intensity-values-selected-World Best Practice Energy Intensity Values for Selectedof the Targets for Energy Intensity and Sulfur Dioxide in

Zhou, Nan

2013-01-01T23:59:59.000Z

26

Contribution of isotopologue self-shielding to sulfur mass-independent fractionation during sulfur dioxide photolysis  

E-Print Network (OSTI)

Signatures of sulfur mass-independent fractionation (S-MIF) are observed for sulfur minerals in Archean rocks, and for modern stratospheric sulfate aerosols (SSA) deposited in polar ice. Ultraviolet light photolysis of ...

Lyons, J. R.

27

Sandia National Laboratories: reducing carbon dioxide emissions  

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

carbon dioxide emissions Measurements of Thermal Stratification in a Homogenous Charge Compression Ignition Engine On February 27, 2013, in CRF, Energy, Facilities, News, News &...

28

Hybrid Microfabricated Device for Field Measurement of Atmospheric Sulfur Dioxide  

Science Journals Connector (OSTI)

It is also now generally agreed that forthcoming major volcanic eruptions will sensitively monitored for increasing sulfur gas emissions as indicated by increasing seismic activity. ... (12)?Fish, B. R.; Durham, J. L. Environ. ...

Shin-Ichi Ohira; Kei Toda; Shin-Ichiro Ikebe; Purnendu K. Dasgupta

2002-10-10T23:59:59.000Z

29

Sulfur dioxide oxidation and plume formation at cement kilns  

SciTech Connect

Results of source sampling at the Glens Falls cement kiln in Glens Falls, N.Y., are reported for sulfur oxides, ammonia, hydrochloric acid, oxygen, and moisture content. The origin of a detached, high-opacity, persistent plume originating from the cement kiln stack is investigated. It is proposed that this plume is due to ammonium salts of SOx and sulfuric acid that have been formed in condensed water droplets in the plume by the pseudocatalytic action of ammonia. (1 diagram, 1 graph, 22 references, 7 tables)

Dellinger, B.; Grotecloss, G.; Fortune, C.R.; Cheney, J.L.; Homolya, J.B.

1980-10-01T23:59:59.000Z

30

From Sulfur Dioxide to Greenhouse Gases: Trends and Events Shaping Future Emissions Trading Programs in the United States  

Science Journals Connector (OSTI)

The success of the United States sulfur dioxide (SO2...) trading program has led to worldwide interest in emissions trading. The program has become a model for ... a theoretical option discussed only by economist...

Joseph Kruger

2007-01-01T23:59:59.000Z

31

Selective catalytic reduction of sulfur dioxide to elemental sulfur. Final report  

SciTech Connect

This project has investigated new metal oxide catalysts for the single stage selective reduction of SO{sub 2} to elemental sulfur by a reductant, such as CO. Significant progress in catalyst development has been made during the course of the project. We have found that fluorite oxides, CeO{sub 2} and ZrO{sub 2}, and rare earth zirconates such as Gd{sub 2}Zr{sub 2}O{sub 7} are active and stable catalysts for reduction Of SO{sub 2} by CO. More than 95% sulfur yield was achieved at reaction temperatures about 450{degrees}C or higher with the feed gas of stoichiometric composition. Reaction of SO{sub 2} and CO over these catalysts demonstrated a strong correlation of catalytic activity with the catalyst oxygen mobility. Furthermore, the catalytic activity and resistance to H{sub 2}O and CO{sub 2} poisoning of these catalysts were significantly enhanced by adding small amounts of transition metals, such as Co, Ni, Co, etc. The resulting transition metal-fluorite oxide composite catalyst has superior activity and stability, and shows promise in long use for the development of a greatly simplified single-step sulfur recovery process to treat variable and dilute SO{sub 2} concentration gas streams. Among various active composite catalyst systems the Cu-CeO{sub 2} system has been extensively studied. XRD, XPS, and STEM analyses of the used Cu-CeO{sub 2} catalyst found that the fluorite crystal structure of ceria was stable at the present reaction conditions, small amounts of copper was dispersed and stabilized on the ceria matrix, and excess copper oxide particles formed copper sulfide crystals of little contribution to catalytic activity. A working catalyst consisted of partially sulfated cerium oxide surface and partially sulfided copper clusters. The overall reaction kinetics were approximately represented by a first order equation.

Liu, W.; Flytzani-Stephanopoulos, M.; Sarofim, A.F.

1995-06-01T23:59:59.000Z

32

On-Road Motor Vehicle Emissions including Ammonia, Sulfur Dioxide and Nitrogen Dioxide Don Stedman, Gary Bishop, Allison Peddle, University of Denver Department of Chemistry and Biochemistry Denver CO 80208. www.feat.biochem.du.edu  

E-Print Network (OSTI)

On-Road Motor Vehicle Emissions including Ammonia, Sulfur Dioxide and Nitrogen Dioxide Don Stedman Nitrogen dioxide: Less than 5% of the NOx BUT with an outstanding peak for the 2007 MY in Fresno 0. Nitrogen dioxide: less than 5% of NOx except the Fresno fleet containing the 2007 Sprinter ambulances. #12;

Denver, University of

33

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

SciTech Connect

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

34

The vibrational and rotational structure of the 2400 to 1950 A? absorption spectrum of sulfur dioxide  

E-Print Network (OSTI)

0. $ ? Vs TBE YiaUSXOKtf U ? m sm U M A L M W of thb 2400 to 1950 2 Ammwim mmmm m s u m m m a m A. BisMrtatiim % James Willbom Biggs, Jfe. Submitted to the Gra4taata Sdtotd tdt HA* Agricultural and Maofcudoal Qtlltc* %ff I'M* 3*i partial... fulfillment of' %hm r*tuir??Mi*s f?r %ift ??' m m m m m m & m s t Major Sttfejoott Rupeio* THE VIBRATIONAL AND ROTATIONAL STRUCTURE OP THE 2400 TO 1950 A ABSORPTION SPECTRUM OP SULFUR DIOXIDE A Dissertation 37 James Willborn Riggs, Jr. Approved...

Riggs, James Willborn

2013-10-04T23:59:59.000Z

35

Oxidation of carbon monoxide and hydrocarbons on platinum and palladium catalysts in the presence of sulfur dioxide  

SciTech Connect

The authors report on a study of the effect of sulfur dioxide on the activity of platinum and palladium catalysts with respect to oxidation of the principal toxic components in the exhaust gases of internal combustion engines: carbon monoxide and hydrocarbons (propylene (C/sub 3/H/sub 6/) and propane (C/sub 3/H/sub 8/)). The experiments were carried out in a flow system equipped with Beckman infrared analyzers to monitor the concentrations of CO and hydrocarbons and of sulfur dioxide. A series of thermal desorption experiments was carried out in a low-pressure flow system with mass spectrometric analysis of the gas phase. The results indicate that the low-temperature adsorption of sulfur dioxide on platinum (and also palladium) catalysts inhibits the oxidation of carbon monoxide and propylene. The poisoning effect of O/sub 2/ is due to blockage of the platinum centers for adsorption of the oxidizable compounds and oxygen.

Panchishnyi, V.I.; Bondareva, N.K.; Sklyarov, A.V.; Rozanov, V.V.; Chadina, G.P.

1988-11-10T23:59:59.000Z

36

Portable instrument and method for detecting reduced sulfur compounds in a gas  

DOE Patents (OSTI)

A portable real time instrument for detecting concentrations in the part per billion range of reduced sulfur compounds in a sample gas. Ozonized air or oxygen and reduced sulfur compounds in a sample gas stream react to produce chemiluminescence in a reaction chamber and the emitted light is filtered and observed by a photomultiplier to detect reduced sulfur compounds. Selective response to individual sulfur compounds is achieved by varying reaction chamber temperature and ozone and sample gas flows, and by the use of either air or oxygen as the ozone source gas.

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

1983-06-01T23:59:59.000Z

37

KINETICS OF OXIDATION OF AQUEOUS SULFUR(IV) BY NITROGEN DIOXIDE YIN-NAN LEE AND STEPHEN E. SCHWARTZ  

E-Print Network (OSTI)

, reagent gas solubilities, mass trans- fer, stoichiometry, and reaction rate were not systematicallyKINETICS OF OXIDATION OF AQUEOUS SULFUR(IV) BY NITROGEN DIOXIDE YIN-NAN LEE AND STEPHEN E. SCHWARTZ for the oxidation of these compounds and their incorpo- ration into atmospheric liquid water are not fully

Schwartz, Stephen E.

38

Modeling of atmospheric corrosion behavior of weathering steel in sulfur dioxide-polluted atmospheres  

SciTech Connect

Atmospheric corrosion resistance of carbon steel (CS) and high-phosphorus weathering steel (WS, Acr-Ten A) was compared after exposure for up to 6 years in Taiwan. In an industrial atmosphere, corrosion kinetics of WS after 3 years of exposure deviated from behavior predicted by the well-known bilogarithmic law. This deviation was simulated using a laboratory accelerated test under cyclic wet/dry conditions with addition of 1 ppm sulfur dioxide (SO{sub 2}). In-situ electrochemical impedance measurements also were carried out in a modified three-electrode cell covered by a thin electrolyte layer to investigate corrosion behavior of WS in SO{sub 2}-polluted environments. Three impedance models were proposed to explain the characteristic corrosion behavior of WS in various stages of exposure.

Wang, J.H.; Shih, H.C. [National Tsing Hua Univ., Hsinchu (Taiwan, Province of China). Dept. of Materials Science and Engineering; Wei, F.I. [China Steel Corp., Kaoshiung (Taiwan, Province of China)

1996-12-01T23:59:59.000Z

39

Remote measurement of sulfur dioxide emissions using an ultraviolet light sensitive video system  

SciTech Connect

Remote measurements of SO/sub 2/ emissions and plume velocities were made with a portable ultraviolet light-sensitive video system and compared with EPA in-stack compliance measurement methods. The instrument system measures the ultraviolet light absorption of SO/sub 2/ and movement of SO/sub 2/ fluctuations in the effluent plume and relates these measurements to the SO/sub 2/ concentration and velocity of the plume. Laboratory and field tests were conducted to establish the potential for using this technique for rapid surveillance of SO/sub 2/ emissions. The effects caused by submicron aerosols also were investigated. The field tests were performed on two occasions. On the first occasion, SO/sub 2/ and plume velocity measurements were made at a typical coal-fired power plant with flue gas desulfurization (FGD) controls (concentrations ranged from 80 to 365 ppm). The second occasion involved participation in an urban particulate modeling study, which resulted in routine SO/sub 2/ emission measurements performed at 12 industrial sites. The results of smoke generator and field tests indicate that the sulfur dioxide concentration of smoke stack emissions can be made with an accuracy less than +/-120 ppm (relative to the EPA stack test compliance method), provided the particulate opacity of the emissions is less than 22 percent. The velocity measurement feature of the instrument correlated poorly with the EPA compliance method for stack gas velocity.

McElhoe, H.B.; Conner, W.D.

1986-01-01T23:59:59.000Z

40

Selective catalytic reduction of sulfur dioxide to elemental sulfur. Quarterly technical progress report No. 6, October--December 1993  

SciTech Connect

Elemental sulfur recovery from SO{sub 2}-containing gas stream is highly attractive as it produces a salable product and no waste to dispose of. However, commercially available schemes are complex and involve multi-stage reactors, such as, most notably in the Resox (reduction of SO{sub 2} with coke) and Claus plant (reaction of SO{sub 2} with H{sub 2}S over catalyst). This project will investigate a cerium oxide catalyst for the single stage selective reduction of SO{sub 2} to elemental sulfur by a reductant, such as carbon monoxide. Cerium oxide has been identified in recent work at MIT as a superior catalyst for SO{sub 2} reduction by CO to elemental sulfur because its high activity and high selectivity to sulfur over COS over a wide temperature range (400--650{degree}C). The detailed kinetic and parametric studies of SO{sub 2} reduction planned in this work over various CeO{sub 2} formulations will provide the necessary basis for development of a very simplified process, namely that of a single-stage elemental sulfur recovery scheme from variable concentration gas streams. The potential cost- and energy-efficiency benefits from this approach can not be overstated. A first apparent application is treatment of a regenerator off-gases in power plants using regenerative flue gas desulfurization. Such a simple catalytic converter may offer the long-sought ``Claus-alternative`` for coal-fired power plant applications.

Liu, W.; Flytzani-Stephanopoulos, M.; Sarofim, A.F.

1993-12-31T23:59:59.000Z

Note: This page contains sample records for the topic "reduce sulfur dioxide" 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 catalytic reduction of sulfur dioxide to elemental sulfur. Quarterly technical progress report No. 4, April--June 1993  

SciTech Connect

Elemental sulfur recovery from SO{sub 2}-containing gas stream is highly attractive as it produces a salable product and no waste to dispose of. However, commercially available schemes are complex and involve multi-stage reactors, such as, most notably in the Resox (reduction of SO{sub 2} with coke) and Claus plant(reaction of SO{sub 2} with H{sub 2}S over catalyst). This project will investigate a cerium oxide catalyst for the single stage selective reduction of SO{sub 2} to elemental sulfur by a reductant, such as carbon monoxide. Cerium oxide has been identified in recent work at MIT as a superior catalyst for SO{sub 2} reduction by CO to elemental sulfur because its high activity and high selectivity to sulfur over COS over a wide temperature range(400--650{degrees}C). The detailed kinetic and parametric studies of SO{sub 2} reduction planned in this work over various CeO{sub 2}-formulations will provide the necessary basis for development of a very simplified process, namely that of a single-stage elemental sulfur recovery scheme from variable concentration gas streams, The potential cost- and energy-efficiency benefits from this approach can not be overstated. A first apparent application is treatment of a regenerator off-gases in power plants using regenerative flue gas desulfurization. Such a simple catalytic converter may offer the long-sought ``Claus-alternative`` for coal-fired power plant applications.

Liu, Wei; Flytzani-Stephanopoulos, M.; Sarofim, A.F.; Williams, R.S.

1993-12-31T23:59:59.000Z

42

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.

43

Selective catalytic reduction of sulfur dioxide to elemental sulfur. Quarterly technical progress report No. 6, October 1993--December 1993  

SciTech Connect

Elemental sulfur recovery from SO{sub 2}-containing gas stream is highly attractive as it produces a salable product and no waste to dispose of. However, commercially available schemes are complex and involve multi-stage reactors, such as, most notably in the Resox (reduction of SO{sub 2} with coke) and Claus plant (reaction of SO{sub 2} with H{sub 2}S over catalyst). This project will investigate a cerium oxide catalyst for the single stage selective reduction of SO{sub 2} to elemental sulfur by a reductant, such as carbon monoxide. Cerium oxide has been identified in recent work at MIT as a superior catalyst for SO{sub 2} reduction by CO to elemental sulfur because its high activity and high selectivity to sulfur over COS over a wide temperature range(400-650 {degrees}C). The detailed kinetic and parametric studies of SO{sub 2} reduction planned in this work over various CeO{sub 2}-formulations will provide the necessary basis for development of a very simplified process, namely that of a single-stage elemental sulfur recovery scheme from variable concentration gas streams. The potential cost- and energy-efficiency benefits from this approach can not be overstated. A first apparent application is treatment of a regenerator off-gases in power plants using regenerative flue gas desulfurization. Such a simple catalytic converter may offer the long-sought {open_quotes}Claus-alternative{close_quotes} for coal-fired power plant applications.

Liu, W.; Flytzani-Stephanopoulos, M.; Sarofim, A.F.

1996-01-01T23:59:59.000Z

44

Elemental sulfur recovery process  

DOE Patents (OSTI)

An improved catalytic reduction process for the direct recovery of elemental sulfur from various SO[sub 2]-containing industrial gas streams. The catalytic process provides combined high activity and selectivity for the reduction of SO[sub 2] to elemental sulfur product with carbon monoxide or other reducing gases. The reaction of sulfur dioxide and reducing gas takes place over certain catalyst formulations based on cerium oxide. The process is a single-stage, catalytic sulfur recovery process in conjunction with regenerators, such as those used in dry, regenerative flue gas desulfurization or other processes, involving direct reduction of the SO[sub 2] in the regenerator off gas stream to elemental sulfur in the presence of a catalyst. 4 figures.

Flytzani-Stephanopoulos, M.; Zhicheng Hu.

1993-09-07T23:59:59.000Z

45

Current emission trends for nitrogen oxides, sulfur dioxide, and volatile organic compounds by month and state: Methodology and results  

SciTech Connect

This report presents estimates of monthly sulfur dioxide (SO{sub 2}), nitrogen oxides (NO{sub x}), and nonmethane voltatile organic compound (VOC) emissions by sector, region, and state in the contiguous United States for the years 1975 through 1988. This work has been funded as part of the National Acid Precipitation Assessment Program`s Emissions and Controls Task Group by the US Department of Energy (DOE) Office of Fossil Energy (FE). The DOE project officer is Edward C. Trexler, DOE/FE Office of Planning and Environment.

Kohout, E.J.; Miller, D.J.; Nieves, L.A.; Rothman, D.S.; Saricks, C.L.; Stodolsky, F.; Hanson, D.A.

1990-08-01T23:59:59.000Z

46

Current emission trends for nitrogen oxides, sulfur dioxide, and volatile organic compounds by month and state: Methodology and results  

SciTech Connect

This report presents estimates of monthly sulfur dioxide (SO{sub 2}), nitrogen oxides (NO{sub x}), and nonmethane voltatile organic compound (VOC) emissions by sector, region, and state in the contiguous United States for the years 1975 through 1988. This work has been funded as part of the National Acid Precipitation Assessment Program's Emissions and Controls Task Group by the US Department of Energy (DOE) Office of Fossil Energy (FE). The DOE project officer is Edward C. Trexler, DOE/FE Office of Planning and Environment.

Kohout, E.J.; Miller, D.J.; Nieves, L.A.; Rothman, D.S.; Saricks, C.L.; Stodolsky, F.; Hanson, D.A.

1990-08-01T23:59:59.000Z

47

Discharge characteristics of lithium/sulfur dioxide (LiSO{sub 2}) ``D`` cells (SAFT America Inc.)  

SciTech Connect

This report presents data which was generated during a series of discharge tests performed on Lithium/Sulfur Dioxide (LiSO{sub 2}) ``D`` cells manufactured by SAFT America Inc., Cockeysville, Maryland. The discharge tests were run using five different load conditions and six temperature regimes. This report contains graphs depicting cell discharge curves (cell voltage versus time). Test results indicate that the cells performed most consistently at temperatures between 0{degrees} and 60{degrees}C and at 10 mA loads. 1 ref., 43 figs.

Pitre, L.J. Jr.

1990-02-01T23:59:59.000Z

48

Evaluation of sulfur-reducing microorganisms for organic desulfurization. [Pyrococcus furiosus  

SciTech Connect

Because of substantial portion of the sulfur in Illinois coal is organic, microbial desulfurization of sulfidic and thiophenic functionalities could hold great potential for completing pyritic sulfur removal. We are testing the hypothesis that organic sulfur can be reductively removed as H{sub 2}S through the activities of anaerobic microorganisms. Our objectives for this year include the following: (1) To obtain cultures that will reductively desulfurize thiophenic model compounds. In addition to crude oil enrichments begun last year, we sampled municipal sewage sludge. (2) To continue to work toward optimizing the activity of the DBDS-reducing cultures obtained during the previous year. (3) To expand coal desulfurization work to include other coals including Illinois Basin Coal 101 and a North Dakota lignite, which might be more susceptible to the dibenzyldisulfide reducing cultures due to its lower rank. (4) To address the problem of sulfide sorption, by investigating the sorption capacity of coals in addition to Illinois Basin Coal 108.

Miller, K.W.

1991-01-01T23:59:59.000Z

49

A composite material of uniformly dispersed sulfur on reduced graphene oxide: Aqueous one-pot synthesis, characterization and excellent performance as the cathode in rechargeable lithium-sulfur batteries  

Science Journals Connector (OSTI)

Sulfur-reduced graphene oxide composite (SGC) materials with uniformly dispersed sulfur on reduced graphene oxide sheets have been prepared by a ... the simultaneous oxidation of sulfide and reduction of graphene

Hui Sun; Gui-Liang Xu; Yue-Feng Xu; Shi-Gang Sun; Xinfeng Zhang…

2012-10-01T23:59:59.000Z

50

Development of a new FGD process that converts sulfur dioxide to salable ammonium phosphate fertilizer  

SciTech Connect

Rich mineral resources have enabled Chinese coal output and energy consumption to rank second and third in the world, respectively. In 1992, up to 70 percent of the country`s electric power was generated by the combustion of some 300 million tons of coal. Although the average sulfur content level in Chinese coals is only about 0.8 percent, the share of high- sulfur coals with 2 percent or more sulfur content is as high as 18 percent. As a result, air pollution accompanied by acid rain now occurs over most of the country, especially in southwestern China. Currently, the area comprising Guangdong, Guangxi, the Sichuan Basin, and the greater part of Gueizhou, where the sulfur content in coal is between 2 and 7 percent and the average pH values of rain water are between 4 and 5 per annum, has become one of the three biggest acid rain-affected areas in the world. In 1992, the national installed coal-fired electricity generation capacity exceeded 100,000 MWe. By the year 2000, it is expected to reach as much as 200,000 MWe, according to a new scheduled program. Environmental pollution caused by large-scale coal combustion is a very important issue that needs to be considered in the implementation of the program. To ensure that the effects of coal-fired power generation on the environment can be properly controlled in the near future, TPRI (Thermal Power Research Institute), the sole thermal power engineering research institution within the Ministry of Electric Power Industry (MOEPI), has conducted a long-term research program to develop sulfur emission control technologies suitable to the special conditions prevalent in China since the early 1970s. The details are summarized. The objective of this chapter is to describe the fundamental concept and major pilot test results and present an economic evaluation of a new process combining flue gas desulfurization (FGD) and ammonium phosphate fertilizer production.

Ji-lu Chen

1993-12-31T23:59:59.000Z

51

Gas chromatographic identification of interferences and their elimination in measuring total reduced sulfur gases  

SciTech Connect

This paper reports on a selective filter that is capable of eliminating positive interference in the coulometric measurement of ambient concentrations of total reduced sulfur gases which has been successfully developed and field tested. Most of the interference was found to be caused by terpenes, which react with bromine, the active reagent in the coulometric titrators. Terpenes are given off by conifer trees in the natural environment as well as emitted in pulping and other wood-handling and lumber manufacturing operations.

de Souza, T.L.C. (Pulp and Paper Research Inst. of Canada, Pointe Claire, PQ (Canada))

1992-05-01T23:59:59.000Z

52

ADVANCED SULFUR CONTROL CONCEPTS  

SciTech Connect

Conventional sulfur removal in integrated gasification combined cycle (IGCC) power plants involves numerous steps: COS (carbonyl sulfide) hydrolysis, amine scrubbing/regeneration, Claus process, and tail-gas treatment. Advanced sulfur removal in IGCC systems involves typically the use of zinc oxide-based sorbents. The sulfides sorbent is regenerated using dilute air to produce a dilute SO{sub 2} (sulfur dioxide) tail gas. Under previous contracts the highly effective first generation Direct Sulfur Recovery Process (DSRP) for catalytic reduction of this SO{sub 2} tail gas to elemental sulfur was developed. This process is currently undergoing field-testing. In this project, advanced concepts were evaluated to reduce the number of unit operations in sulfur removal and recovery. Substantial effort was directed towards developing sorbents that could be directly regenerated to elemental sulfur in an Advanced Hot Gas Process (AHGP). Development of this process has been described in detail in Appendices A-F. RTI began the development of the Single-step Sulfur Recovery Process (SSRP) to eliminate the use of sorbents and multiple reactors in sulfur removal and recovery. This process showed promising preliminary results and thus further process development of AHGP was abandoned in favor of SSRP. The SSRP is a direct Claus process that consists of injecting SO{sub 2} directly into the quenched coal gas from a coal gasifier, and reacting the H{sub 2}S-SO{sub 2} mixture over a selective catalyst to both remove and recover sulfur in a single step. The process is conducted at gasifier pressure and 125 to 160 C. The proposed commercial embodiment of the SSRP involves a liquid phase of molten sulfur with dispersed catalyst in a slurry bubble-column reactor (SBCR).

Apostolos A. Nikolopoulos; Santosh K. Gangwal; William J. McMichael; Jeffrey W. Portzer

2003-01-01T23:59:59.000Z

53

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

54

Reducing Carbon Dioxide Emissions with Enhanced Oil Recovery Projects:? A Life Cycle Assessment Approach  

Science Journals Connector (OSTI)

Reducing Carbon Dioxide Emissions with Enhanced Oil Recovery Projects:? A Life Cycle Assessment Approach ... This capacity corresponds approximately to storing the emissions of a 5 MW power plant emitting 65 tons of CO2 per day for almost 1800 years27 or 14 years from a 300 MW coal power plant where 8000 tons of CO2 is captured per day. ... To overcome this CO2 emission problem, there is great interest, esp. in Canada, to capture carbon dioxide and utilize it as a flooding agent for the enhanced oil recovery (EOR) process. ...

Anne-Christine Aycaguer; Miriam Lev-On; Arthur M. Winer

2001-03-01T23:59:59.000Z

55

Ground level concentration of sulfur dioxide at Kuwait`s major population centers during the oil-field fires  

SciTech Connect

During the Iraqi occupation, Kuwait`s oil wells were ignited. the fires were damaging to the country`s oil resources and air quality. The impact of the oil-field fires on the air quality was studied to determine the level of exposure to pollutants in major population centers. The period of July-September 1991 was selected for examination. A mathematical model was used to compute the ground-level concentration isopleths. The results of these computations are supported by significant concentrations measured and reported by the Environmental Protection Council, Kuwait. The ground-level concentrations of sulfur dioxide in the major population centers, whether measure or estimated, were less than the ambient standards of the U.S. Environmental Protection Agency`s air pollution index. The dispersive characteristics were classified according to wind conditions. The results of this assessment provide historical data on Kuwait`s oil fires and may be useful in assessing risks resulting from this catastrophe. 6 refs., 10 fig., 2 tab.

Al-Ajmi, D.N.; Marmoush, Y.R. [Kuwait Institute for Scientific Research (Kuwait)] [Kuwait Institute for Scientific Research (Kuwait)

1996-08-01T23:59:59.000Z

56

U.S. Sulfur Dioxide Emissions Trading Program: Results and Further Applications  

Science Journals Connector (OSTI)

The use of emissions trading (cap and trade) is gaining worldwide...2 have been reduced annually from sources participating in the US SO2 emissions trading program. Ambient SO2 levels and sulfate deposition have ...

Stephanie Rose Benkovic; Joseph Kruger

2001-08-01T23:59:59.000Z

57

Advances of flue gas desulfurization technology for coal-fired boilers and strategies for sulfur dioxide pollution prevention in China  

SciTech Connect

Coal is one of the most important kinds of energy resources at the present time and in the immediate future in China. Sulfur dioxide resulting from combustion of coal is one of the principle pollutants in the air. Control of SO{sub 2} discharge is still a major challenge for environmental protection in developing China. In this paper, research, development and application of technology of flue gas desulfurization (FGD) for coal-fired boilers in China will be reviewed with emphasis on cost-effective technology, and the development trends of FGD technology, as well as the strategy for SO{sub 2} discharge control in China, will be analyzed. A practical technology for middle-small-sized boilers developed by the primary author and the field investigation results will also be presented. At present, there are four major kinds of FGD technologies that are practical to be applied in China for their cost-effectiveness and efficiency to middle-small-sized boilers. An important development trend of the FGD technology for middle-small-sized boilers for the next decade is improvement of the existing cost-effective wet-type FGD technology, and in the future it will be the development of dry-type FGD technology. For middle-sized generating boilers, the development direction of the FGD technology is the spraying and drying process. For large-sized generating boilers, the wet-type limestone-plaster process will still be applied in the immediate future, and dry-type FGD technologies, such as ammonia with electron beam irradiation, will be developed in the future. State strategies for the control of SO{sub 2} discharge will involve the development and popularization of efficient coal-fired devices, extension of gas coal and liquefied coal, spreading coal washing, and centralized heating systems.

Yang, C.; Zeng, G.; Li, G.; Qiu, J.

1999-07-01T23:59:59.000Z

58

Comparison of thermoelectric and permeation dryers for sulfur dioxide removal during sample conditioning of wet gas streams  

SciTech Connect

Flue gas conditioning for moisture removal is commonly performed for criteria pollutant measurements, in particular for extractive CEM systems at combustion sources. An implicit assumption is that conditioning systems specifically remove moisture without affecting pollutant and diluent concentrations. Gas conditioning is usually performed by passing the flue gas through a cold trap (Peltier or thermoelectric dryer) to remove moisture by condensation, which is subsequently extracted by a peristaltic pump. Many air pollutants are water-soluble and potentially susceptible to removal in a condensation dryer from gas interaction with liquid water. An alternative technology for gas conditioning is the permeation dryer, where the flue gas passes through a selectively permeable membrane for moisture removal. In this case water is transferred through the membrane while other pollutants are excluded, and the gas does not contact condensed liquid. Laboratory experiments were performed to measure the relative removal of a water-soluble pollutant (sulfur dioxide, SO{sub 2}) by the two conditioning techniques. A wet gas generating system was used to create hot, wet gas streams of known composition (15% and 30% moisture, balance nitrogen) and flow rate. Pre-heated SO{sub 2} was dynamically spiked into the wet stream using mass flow meters to achieve concentrations of 20, 50, and 100 ppm. The spiked gas was directed through a heated sample line to either a thermoelectric or a permeation conditioning system. Two gas analyzers (Western Research UV gas monitor, KVB/Analect FTIR spectrometer) were used to measure the SO{sub 2} concentration after conditioning. Both analytic methods demonstrated that SO{sub 2} is removed to a significantly greater extent by the thermoelectric dryer. These results have important implications for SO{sub 2} monitoring and emissions trading.

Dunder, T.A. [Entropy, Inc., Research Triangle Park, NC (United States). Research Div.; Leighty, D.A. [Perma Pure, Inc., Toms River, NJ (United States)

1997-12-31T23:59:59.000Z

59

Catalyst for elemental sulfur recovery process  

DOE Patents (OSTI)

A catalytic reduction process is described for the direct recovery of elemental sulfur from various SO[sub 2]-containing industrial gas streams. The catalytic process provides high activity and selectivity, as well as stability in the reaction atmosphere, for the reduction of SO[sub 2] to elemental sulfur product with carbon monoxide or other reducing gases. The reaction of sulfur dioxide and reducing gas takes place over a metal oxide composite catalyst having one of the following empirical formulas: [(FO[sub 2])[sub 1[minus]n](RO)[sub n

Flytzani-Stephanopoulos, M.; Liu, W.

1995-01-24T23:59:59.000Z

60

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.

Note: This page contains sample records for the topic "reduce sulfur dioxide" 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

Clarification of C-S relationships of marine black shales using stable isotopic composition of reduced sulfur  

SciTech Connect

Carbon-sulfur relationships are compared for the Miocene Monterey Formation (Santa Maria Basin, California) and the Upper Devonian New Albany Shale (Illinois Basin, Indiana). In both formations, C-S concentrations covary for samples with the lower to more intermediate organic carbon concentrations and become invariant at higher organic carbon concentrations. While the similarity of these relationships in Monterey and New Albany suggest sulfur diagenesis occurred in similar depositional environments, sulfur isotopic data clearly indicate differences in the depositional environments. In the Monterey, the most organic-rich laminated shales are characterized by isotopic enrichment of reduced S and low S ratios and indicate that sulfate reduction occurred under sulfate-limited conditions within the sediments. In the New Albany, organic-rich laminated shales exhibit isotopic depletion of reduced S coupled with low S[sub reduced]/C[sub org] and suggest sulfur diagenesis occurred under euxinic conditions. These data show that in the absence of sulfur isotopic data, misleading conclusions concerning depositional environments can be made when using C-S plots and the traditional interpretations that are associated with these types of plots.

Zaback, D.A.; Pratt, L.M. (Indiana Univ., Bloomington, IN (United States). Dept. of Geological Sciences)

1992-01-01T23:59:59.000Z

62

Evaluation of sulfur-reducing microorganisms for organic desulfurization. Final technical report, September 1, 1990--August 31, 1991  

SciTech Connect

Because of substantial portion of the sulfur in Illinois coal is organic, microbial desulfurization of sulfidic and thiophenic functionalities could hold great potential for completing pyritic sulfur removal. We are testing the hypothesis that organic sulfur can be reductively removed as H{sub 2}S through the activities of anaerobic microorganisms. Our objectives for this year include the following: (1) To obtain cultures that will reductively desulfurize thiophenic model compounds. In addition to crude oil enrichments begun last year, we sampled municipal sewage sludge. (2) To continue to work toward optimizing the activity of the DBDS-reducing cultures obtained during the previous year. (3) To expand coal desulfurization work to include other coals including Illinois Basin Coal 101 and a North Dakota lignite, which might be more susceptible to the dibenzyldisulfide reducing cultures due to its lower rank. (4) To address the problem of sulfide sorption, by investigating the sorption capacity of coals in addition to Illinois Basin Coal 108.

Miller, K.W.

1991-12-31T23:59:59.000Z

63

RECENT ADVANCES IN THE DEVELOPMENT OF THE HYBRID SULFUR PROCESS FOR HYDROGEN PRODUCTION  

SciTech Connect

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. In the HyS Process, sulfur dioxide is oxidized in the presence of water at the electrolyzer anode to produce sulfuric acid and protons. The protons are transported through a cation-exchange membrane electrolyte to the cathode and are reduced to form hydrogen. In the second stage of the process, the sulfuric acid by-product from the electrolyzer is thermally decomposed at high temperature to produce sulfur dioxide and oxygen. The two gases are separated and the sulfur dioxide recycled to the electrolyzer for oxidation. The Savannah River National Laboratory (SRNL) has been exploring a fuel-cell design concept for the SDE using an anolyte feed comprised of concentrated sulfuric acid saturated with sulfur dioxide. The advantages of this design concept include high electrochemical efficiency and small footprint compared to a parallel-plate electrolyzer design. This paper will provide a summary of recent advances in the development of the SDE for the HyS process.

Hobbs, D.

2010-07-22T23:59:59.000Z

64

Electrochemical studies of the corrosion behavior of carbon and weathering steels in alternating wet/dry environments with sulfur dioxide gas  

SciTech Connect

Electrochemical impedance techniques were used to investigate the corrosion behavior of carbon steel (CS) and weathering steel (WS) in sulfur dioxide (SO{sub 2})-containing environments. Impedance measurements were conducted in a modified three-electrode electrochemical cell covered by a thin electrolyte layer during the wet/dry period. Results showed WS was more resistant to SO{sub 2}-induced atmospheric corrosion than CS. Three forms of impedance spectra were observed, depending upon exposure period. Accordingly, three impedance models were proposed to explain the characteristic impedance data and corrosion behaviors in different stages of exposure. The proposed models and equivalent circuits produced good agreement with experimental impedance data.

Wang, J.H.; Shih, H.C. [National Tsing Hua Univ., Hsinchu (Taiwan, Province of China). Dept. of Materials Science and Engineering; Wei, F.I. [China Steel Corp., Kaoshiung (Taiwan, Province of China)

1996-08-01T23:59:59.000Z

65

Notification to Mirant by the Commonwealth of Virginia of Serious Violations of the National Ambient Air Quality Standards for Sulfur Dioxide  

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

9, 2005 9, 2005 Lisa D. Johnson, President Mirant Potomac River, LLC 8711 Westphalia Road Upper Marlboro, Maryland 20774 Dear Ms. Johnson: DEQ is in receipt of the results of Mirant's "downwash" modeling provided by Mirant to DEQ pursuant to the consent special order between the State Air Pollution Control Board and Mirant Potomac River, LLC. A cursory review of the modeling reveals that emissions from the Potomac River Generating Station result in, cause or substantially contribute to serious violations of the primary national ambient air quality standards or "NAAQS" for sulfur dioxide (SO 2 ), nitrogen dioxide (NO 2 ) and PM 10 . NAAQS are established by the U. S. Environmental Protection Agency at concentrations necessary to protect human health with an adequate margin of safety.

66

Efficient Conversion of Thermal Energy into Hydrogen: Comparing Two Methods to Reduce Exergy Losses in a Sulfuric Acid Decomposition Reactor  

Science Journals Connector (OSTI)

Efficient Conversion of Thermal Energy into Hydrogen: Comparing Two Methods to Reduce Exergy Losses in a Sulfuric Acid Decomposition Reactor ... The first design uses optimal control theory to obtain a more uniform distribution of the entropy production. ... This optimized design is found to perform the best, but it requires significant changes in the heating equipment in order to approximately realize the optimal temperature profiles. ...

Leen V. van der Ham; Joachim Gross; Ad Verkooijen; Signe Kjelstrup

2009-08-06T23:59:59.000Z

67

Lubricant oil consumption effects on diesel exhaust ash emissions using a sulfur dioxide trace technique and thermogravimetry  

E-Print Network (OSTI)

A detailed experimental study was conducted targeting lubricant consumption effects on ,diesel exhaust ash levels using a model year 2002 5.9L diesel engine, high and low Sulfur commercial lubricants, and clean diesel ...

Plumley, Michael J

2005-01-01T23:59:59.000Z

68

High Purity Hydrogen Production with In-Situ Carbon Dioxide and Sulfur Capture in a Single Stage Reactor  

SciTech Connect

Enhancement in the production of high purity hydrogen (H{sub 2}) from fuel gas, obtained from coal gasification, is limited by thermodynamics of the water gas shift (WGS) reaction. However, this constraint can be overcome by conducting the WGS in the presence of a CO{sub 2}-acceptor. The continuous removal of CO{sub 2} from the reaction mixture helps to drive the equilibrium-limited WGS reaction forward. Since calcium oxide (CaO) exhibits high CO{sub 2} capture capacity as compared to other sorbents, it is an ideal candidate for such a technique. The Calcium Looping Process (CLP) developed at The Ohio State University (OSU) utilizes the above concept to enable high purity H{sub 2} production from synthesis gas (syngas) derived from coal gasification. The CLP integrates the WGS reaction with insitu CO{sub 2}, sulfur and halide removal at high temperatures while eliminating the need for a WGS catalyst, thus reducing the overall footprint of the hydrogen production process. The CLP comprises three reactors - the carbonator, where the thermodynamic constraint of the WGS reaction is overcome by the constant removal of CO{sub 2} product and high purity H{sub 2} is produced with contaminant removal; the calciner, where the calcium sorbent is regenerated and a sequestration-ready CO{sub 2} stream is produced; and the hydrator, where the calcined sorbent is reactivated to improve its recyclability. As a part of this project, the CLP was extensively investigated by performing experiments at lab-, bench- and subpilot-scale setups. A comprehensive techno-economic analysis was also conducted to determine the feasibility of the CLP at commercial scale. This report provides a detailed account of all the results obtained during the project period.

Nihar Phalak; Shwetha Ramkumar; Daniel Connell; Zhenchao Sun; Fu-Chen Yu; Niranjani Deshpande; Robert Statnick; Liang-Shih Fan

2011-07-31T23:59:59.000Z

69

Intention to change activities that reduce carbon dioxide emissions related to worry about global climate change consequences  

Science Journals Connector (OSTI)

Introduction Mitigating the global climate change requires actions at different levels including that lay people change their consumption patterns, which cause emissions of greenhouse gases. Recent research suggests that inducing affects such as fear and worry may have positive effects. Objective To investigate whether worry in addition to personalized information about emissions of carbon dioxide would influence lay people's intentions to change consumption-related personal activities causing carbon-dioxide emissions. Method A municipality-provided tool to calculate their annual carbon dioxide emissions was used by 135 university students who after being informed about negative consequences of global climate change stated their intentions to change a number of personal activities to reduce carbon dioxide emissions during the following 12 months. They also rated how worried they were about eight global climate change consequences. Results Intentions to change travel, energy use at home, food consumption, involvement in environmental organizations, and support of environmental policies increased with worry. An interaction was also observed such that high-emitters’ intentions to invest in energy-efficient infrastructure increased more with worry than did low- and medium-emitters’ intentions. Conclusions In line with recent research positing that affect increases preventive actions, the hypothesis was supported that intentions to change personal activities to reduce carbon dioxide emissions increased with participants’ worry about the consequences of global climate change.

E.-L. Sundblad; A. Biel; T. Gärling

2014-01-01T23:59:59.000Z

70

Applications of carbon dioxide capture and storage technologies in reducing emissions from fossil-fired power plants  

SciTech Connect

The aim of this paper is to investigate the global contribution of carbon capture and storage technologies to mitigating climate change. Carbon capture and storage is a technology that comprises the separation of from carbon dioxide industrial- and energy-related sources, transport to a storage location (e.g., saline aquifers and depleted hydrocarbon fields), and long-term isolation from the atmosphere. The carbon dioxides emitted directly at the power stations are reduced by 80 to 90%. In contrast, the life cycle assessment shows substantially lower reductions of greenhouse gases in total (minus 65 to 79%).

Balat, M.; Balat, H.; Oz, C. [University of Mahallesi, Trabzon (Turkey)

2009-07-01T23:59:59.000Z

71

Calcium looping process for high purity hydrogen production integrated with capture of carbon dioxide, sulfur and halides  

DOE Patents (OSTI)

A process for producing hydrogen comprising the steps of: (i) gasifying a fuel into a raw synthesis gas comprising CO, hydrogen, steam, sulfur and halide contaminants in the form of H.sub.2S, COS, and HX, wherein X is a halide; (ii) passing the raw synthesis gas through a water gas shift reactor (WGSR) into which CaO and steam are injected, the CaO reacting with the shifted gas to remove CO.sub.2, sulfur and halides in a solid-phase calcium-containing product comprising CaCO.sub.3, CaS and CaX.sub.2; (iii) separating the solid-phase calcium-containing product from an enriched gaseous hydrogen product; and (iv) regenerating the CaO by calcining the solid-phase calcium-containing product at a condition selected from the group consisting of: in the presence of steam, in the presence of CO.sub.2, in the presence of synthesis gas, in the presence of H.sub.2 and O.sub.2, under partial vacuum, and combinations thereof.

Ramkumar, Shwetha; Fan, Liang-Shih

2013-07-30T23:59:59.000Z

72

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

E-Print Network (OSTI)

committed to reduce its carbon intensity (CO 2 per unit ofcommitted to reduce its carbon intensity (CO 2 per unit of2 emissions, and the 40-45% carbon intensity reduction goals

Zhou, Nan

2013-01-01T23:59:59.000Z

73

COMPONENT DEVELOPMENT NEEDS FOR THE HYBRID SULFUR ELECTROLYZER  

SciTech Connect

Fiscal year 2008 studies in electrolyzer component development have focused on the characterization of membrane electrode assemblies (MEA) after performance tests in the single cell electrolyzer, evaluation of electrocatalysts and membranes using a small scale electrolyzer and evaluating the contribution of individual cell components to the overall electrochemical performance. Scanning electron microscopic (SEM) studies of samples taken from MEAs testing in the SRNL single cell electrolyzer test station indicates a sulfur-rich layer forms between the cathode catalyst layer and the membrane. Based on a review of operating conditions for each of the MEAs evaluated, we conclude that the formation of the layer results from the reduction of sulfur dioxide as it passes through the MEA and reaches the catalyst layer at the cathode-membrane interface. Formation of the sulfur rich layer results in partial delamination of the cathode catalyst layer leading to diminished performance. Furthermore we believe that operating the electrolyzer at elevated pressure significantly increases the rate of formation due to increased adsorption of hydrogen on the internal catalyst surface. Thus, identification of a membrane that exhibits much lower transport of sulfur dioxide is needed to reduce the quantity of sulfur dioxide that reaches the cathode catalyst and is reduced to produce the sulfur-rich layer. Three candidate membranes are currently being evaluated that have shown promise from preliminary studies, (1) modified Nafion{reg_sign}, (2) polybenzimidazole (PBI), and (3) sulfonated Diels Alder polyphenylene (SDAPP). Testing examined the activity for the sulfur dioxide oxidation of platinum (Pt) and platinum-alloy catalysts in 30 wt% sulfuric acid solution. Linear sweep voltammetry showed an increase in activity when catalysts in which Pt is alloyed with non-noble transition metals such as cobalt and chromium. However when Pt is alloyed with noble metals, such as iridium or ruthenium, the kinetic activity decreases. We recommend further testing to determine if these binary alloys will provide the increased reaction kinetic needed to meet the targets. We also plan to test the performance of these catalyst materials for both proton and sulfur dioxide reduction. The latter may provide another parameter by which we can control the reduction of sulfur dioxide upon transport to the cathode catalyst surface. A small scale electrolyzer (2 cm{sup 2}) has been fabricated and successfully installed as an additional tool to evaluate the effect of different operating conditions on electrolyzer and MEA performance. Currently this electrolyzer is limited to testing at temperatures up to 80 C and at atmospheric pressure. Selected electrochemical performance data from the single cell sulfur dioxide depolarized electrolyzer were analyzed with the aid of an empirical equation which takes into account the overpotential of each of the components. By using the empirical equation, the performance data was broken down into its components and a comparison of the potential losses was made. The results indicated that for the testing conditions of 80 C and 30 wt% sulfuric acid, the major overpotential contribution ({approx}70 % of all losses) arise from the slow reaction rate of oxidation of sulfur dioxide. The results indicate that in order to meet the target of hydrogen production at 0.5 A/cm{sup 2} at 0.6 V and 50 wt% sulfuric acid, identification of a better catalyst for sulfur dioxide oxidation will provide the largest gain in electrolyzer performance.

Hobbs, D; Hector Colon-Mercado, H; Mark Elvington, M

2008-05-30T23:59:59.000Z

74

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

E-Print Network (OSTI)

controls or integrated measures could simultaneously reduce greenhouse gas (GHG) emissions and criteria air pollutantcontrols or integrated measures that simultaneously reduce greenhouse gas (GHG) emissions and criteria air pollutantcontrols or integrated measures that are defined as simultaneously reducing greenhouse gas (GHG) emissions and criteria air pollutant

Zhou, Nan

2013-01-01T23:59:59.000Z

75

METHOD TO PREVENT SULFUR ACCUMULATION INSIDE MEMBRANE ELECTRODE ASSEMBLY  

SciTech Connect

HyS is conceptually the simplest of the thermochemical cycles and involves only sulfur chemistry. In the HyS Cycle hydrogen gas (H{sub 2}) is produced at the cathode of the electrochemical cell (or electrolyzer). Sulfur dioxide (SO{sub 2}) is oxidized at the anode to form sulfuric acid (H{sub 2}SO{sub 4}) and protons (H{sup +}) as illustrated below. A separate high temperature reaction decomposes the sulfuric acid to water and sulfur dioxide which are recycled to the electrolyzers, and oxygen which is separated out as a secondary product. The electrolyzer includes a membrane that will allow hydrogen ions to pass through but block the flow of hydrogen gas. The membrane is also intended to prevent other chemical species from migrating between electrodes and undergoing undesired reactions that could poison the cathode or reduce overall process efficiency. In conventional water electrolysis, water is oxidized at the anode to produce protons and oxygen. The standard cell potential for conventional water electrolysis is 1.23 volts at 25 C. However, commercial electrolyzers typically require higher voltages ranging from 1.8 V to 2.6 V [Kirk-Othmer, 1991]. The oxidation of sulfur dioxide instead of water in the HyS electrolyzer occurs at a much lower potential. For example, the standard cell potential for sulfur dioxide oxidation at 25 C in 50 wt % sulfuric acid is 0.29 V [Westinghouse, 1980]. Since power consumption by the electrolyzers is equal to voltage times current, and current is proportional to hydrogen production, a large reduction in voltage results in a large reduction in electrical power cost per unit of hydrogen generated.

Steimke, J.; Steeper, T.; Herman, D.; Colon-Mercado, H.; Elvington, M.

2009-06-22T23:59:59.000Z

76

Hydrogenase of the hyperthermophile Pyrococcus furiosus is an elemental sulfur reductase or sulfhydrogenase: evidence for a sulfur-reducing hydrogenase ancestor  

Science Journals Connector (OSTI)

...polysulfide reduction/geothermal biolog/evolution...appears to be an energy-conserving reaction...The publication costs of this article...sulfur-rich, geothermal environ- ments...fact, represent an energy- conserving reaction...the Department of Energy (FG09-88ER13901...

K Ma; R N Schicho; R M Kelly; M W Adams

1993-01-01T23:59:59.000Z

77

Impact of additives for enhanced sulfur dioxide removal on re-emissions of mercury in wet flue gas desulfurization  

Science Journals Connector (OSTI)

Abstract The wet flue gas desulfurization process (FGD) in fossil fired power plants offers the advantage of simultaneously removing SO2 and other water soluble pollutants, such as certain oxidized mercury compounds (Hg2+). In order to maximize SO2 removal efficiency of installed FGD units, organic additives can be utilized. In the context of multi-pollutant control by wet FGD, the effect of formic and adipic acid on redox reactions of dissolved mercury compounds is investigated with a continuously operated lab-scale test-rig. For sulfite ( SO 3 2 - ) concentrations above a certain critical value, their potential as reducing agent leads to rapidly increasing formation and re-emission of elemental mercury (Hg0). Increasing chloride concentration and decreasing pH and slurry temperature have been identified as key factors for depressing Hg0 re-emissions. Both organic additives have a negative impact on Hg-retention and cause increased Hg0 re-emissions in the wet FGD process, with formic acid being the significantly stronger reducing agent. Different pathways of Hg2+ reduction were identified by qualitative interpretation of the pH-dependence and by comparison of activation enthalpies and activation entropies. While the first mechanism proposed identifies SO 3 2 - as reducing agent and is therefore relevant for any FGD process, the second mechanism involves the formate anion, thus being exclusively relevant for \\{FGDs\\} utilizing formic acid as additive.

Barna Heidel; Melanie Hilber; Günter Scheffknecht

2014-01-01T23:59:59.000Z

78

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

SciTech Connect

Since 2006, China has set goals of reducing energy intensity, emissions, and pollutants in multiple guidelines and in the Five Year Plans. Various strategies and measures have then been taken to improve the energy efficiency in all sectors and to reduce pollutants. Since controlling energy, CO{sub 2} emissions, and pollutants falls under the jurisdiction of different government agencies in China, many strategies are being implemented to fulfill only one of these objectives. Co-controls or integrated measures could simultaneously reduce greenhouse gas (GHG) emissions and criteria air pollutant emissions. The targets could be met in a more cost effective manner if the integrated measures can be identified and prioritized. This report provides analysis and insights regarding how these targets could be met via co-control measures focusing on both CO{sub 2} and SO{sub 2} emissions in the cement, iron &steel, and power sectors to 2030 in China. An integrated national energy and emission model was developed in order to establish a baseline scenario that was used to assess the impact of actions already taken by the Chinese government as well as planned and expected actions. In addition, CO{sub 2} mitigation scenarios and SO{sub 2} control scenarios were also established to evaluate the impact of each of the measures and the combined effects. In the power sector, although the end of pipe SO{sub 2} control technology such as flue gas desulfurization (FGD) has the largest reduction potential for SO{sub 2} emissions, other CO{sub 2} control options have important co-benefits in reducing SO{sub 2} emissions of 52.6 Mt of SO{sub 2} accumulatively. Coal efficiency improvements along with hydropower, renewable and nuclear capacity expansion will result in more than half of the SO{sub 2} emission reductions as the SO{sub 2} control technology through 2016. In comparison, the reduction from carbon capture and sequestration (CCS) is much less and has negative SO{sub 2} reductions potential. The expanded biomass generation scenario does not have significant potential for reducing SO{sub 2} emissions, because of its limited availability. For the cement sector, the optimal co-control strategy includes accelerated adoption of energy efficiency measures, decreased use of clinker in cement production, increased use of alternative fuels, and fuel-switching to biomass. If desired, additional SO{sub 2} mitigation could be realized by more fully adopting SO{sub 2} abatement mitigation technology measures. The optimal co-control scenario results in annual SO{sub 2} emissions reductions in 2030 of 0.16 Mt SO{sub 2} and annual CO{sub 2} emissions reductions of 76 Mt CO{sub 2}. For the iron and steel sector, the optimal co-control strategy includes accelerated adoption of energy efficiency measures, increased share of electric arc furnace steel production, and reduced use of coal and increased use of natural gas in steel production. The strategy also assumes full implementation of sinter waste gas recycling and wet desulfurization. This strategy results in annual SO{sub 2} emissions reductions in 2030 of 1.3 Mt SO{sub 2} and annual CO{sub 2} emissions reductions of 173 Mt CO{sub 2}.

Zhou, Nan; Price, Lynn; Zheng, Nina; Ke, Jing; Hasanbeigi, Ali

2011-10-15T23:59:59.000Z

79

Analysis of Strategies for Reducing Multiple Emissions from Electric Power Plants: SO2, Nox, CO2  

Reports and Publications (EIA)

This report responds to a request received from Senator David McIntosh on June 29, 2000 to analyze the impacts on energy consumers and producers of coordinated strategies to reduce emissions of sulfur dioxide, nitrogen oxides, and carbon dioxide at U.S. power plants.

2001-01-01T23:59:59.000Z

80

Method to prevent sulfur accumulation in membrane electrode assembly  

DOE Patents (OSTI)

A method of operating a hybrid sulfur electrolyzer to generate hydrogen is provided that includes the steps of providing an anolyte with a concentration of sulfur dioxide, and applying a current. During steady state generation of hydrogen a plot of applied current density versus concentration of sulfur dioxide is below a boundary line. The boundary line may be linear and extend through the origin of the graph with a slope of 0.001 in which the current density is measured in mA/cm2 and the concentration of sulfur dioxide is measured in moles of sulfur dioxide per liter of anolyte.

Steimke, John L; Steeper, Timothy J; Herman, David T

2014-04-29T23:59:59.000Z

Note: This page contains sample records for the topic "reduce sulfur dioxide" 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

A Novel Collaboration Paradigm for Reducing Energy Consumption and Carbon Dioxide Emissions in Data Centres  

Science Journals Connector (OSTI)

......research and innovation projects to reduce the energy consumption The Computer...this topic. This research project designed energy-aware optimization policies...an unpredicted renewable energy surplus (typically solar or wind). This low emission......

D. Rincón; A. Agustí-Torra; J.F. Botero; F. Raspall; D. Remondo; X. Hesselbach; M.T. Beck; H. de Meer; F. Niedermeier; G. Giuliani

2013-12-01T23:59:59.000Z

82

A Novel Collaboration Paradigm for Reducing Energy Consumption and Carbon Dioxide Emissions in Data Centres  

Science Journals Connector (OSTI)

......consumption can be reduced (or increased) in periods of power generation shortage (or surplus). In the context of Smart Grid technologies, this can even be extended to average or even minor customers. 3. ARCHITECTURE OVERVIEW In Fig. 3......

D. Rincón; A. Agustí-Torra; J.F. Botero; F. Raspall; D. Remondo; X. Hesselbach; M.T. Beck; H. de Meer; F. Niedermeier; G. Giuliani

2013-12-01T23:59:59.000Z

83

Using ISC & GIS to predict sulfur deposition from coal-fired power plants  

E-Print Network (OSTI)

The goal of this research project was to determine if atmospheric sources have the potential of contributing significantly to the sulfur content of grazed forage. Sulfur deposition resulting from sulfur dioxide emissions from coal- fired power...

Lopez, Jose Ignacio

2012-06-07T23:59:59.000Z

84

A Novel Collaboration Paradigm for Reducing Energy Consumption and Carbon Dioxide Emissions in Data Centres  

Science Journals Connector (OSTI)

......since power generation is based on fossil fuels. Therefore, to reduce expenses and its...renewable sources is free of costs for fuel, but to be able to compensate, the EP...collateral effects (for example, UPS batteries can degrade after successive charge......

D. Rincón; A. Agustí-Torra; J.F. Botero; F. Raspall; D. Remondo; X. Hesselbach; M.T. Beck; H. de Meer; F. Niedermeier; G. Giuliani

2013-12-01T23:59:59.000Z

85

Sulfur capture in combination bark boilers  

SciTech Connect

A review of sulfur dioxide emission data for eight combination bark boilers in conjunction with the sulfur contents of the fuels reveals significant sulfur capture ranging from 10% to over 80% within the solid ash phase. Wood ash characteristics similar to activated carbon as well as the significant wood ash alkali oxide and carbonate fractions are believed responsible for the sulfur capture. Sulfur emissions from combination bark-fossil fuel firing are correlated to the sulfur input per ton of bark or wood residue fired.

Someshwar, A.V.; Jain, A.K. (National Council of the Paper Industry for Air and Stream Improvement, Gainesville, FL (United States))

1993-07-01T23:59:59.000Z

86

FY08 MEMBRANE CHARACTERIZATION REPORT FOR HYBRID SULFUR ELECTROLYZER  

SciTech Connect

This report summarizes results from all of the membrane testing completed to date at the Savannah River National Laboratory (SRNL) for the sulfur dioxide-depolarized electrolyzer (SDE). Several types of commercially-available membranes have been analyzed for ionic resistance and sulfur dioxide transport including perfluorinated sulfonic acid (PFSA), sulfonated polyether-ketone-ketone (SPEKK), and polybenzimidazole membranes (PBI). Of these membrane types, the poly-benzimidazole membrane, Celtec-L, exhibited the best combination of characteristics for use in an SDE. Several experimental membranes have also been analyzed including hydrated sulfonated Diels-Alder polyphenylenes (SDAPP) membranes from Sandia National Laboratory, perfluorosulfonimide (PFSI) and sulfonated perfluorocyclobutyl aromatic ether (S-PFCB) prepared by Clemson University, hydrated platinum-treated PFSA prepared by Giner Electrochemical Systems (GES) and Pt-Nafion{reg_sign} 115 composites prepared at SRNL. The chemical stability, SO{sub 2} transport and ionic conductivity characteristics have been measured for several commercially available and experimental proton-conducting membranes. Commercially available PFSA membranes such as the Nafion{reg_sign} series exhibited excellent chemical stability and ionic conductivity in sulfur dioxide saturated sulfuric acid solutions. Sulfur dioxide transport in the Nafion{reg_sign} membranes varied proportionally with the thickness and equivalent weight of the membrane. Although the SO{sub 2} transport in the Nafion{reg_sign} membranes is higher than desired, the excellent chemical stability and conductivity makes this membrane the best commercially-available membrane at this time. Initial results indicated that a modified Nafion{reg_sign} membrane incorporating Pt nanoparticles exhibited significantly reduced SO{sub 2} transport. Reduced SO{sub 2} transport was also measured with commercially available PBI membrane and several experimental membranes produced at SNL and Clemson. These membranes also exhibit good chemical stability and conductivity in concentrated sulfuric acid solutions and, thus, serve as promising candidates for the SDE. Therefore, we recommend further testing of these membranes including electrolyzer testing to determine if the reduced SO{sub 2} transport eliminates the formation of sulfur-containing films at the membrane/cathode interface. SO{sub 2} transport measurements in the custom built characterization cell identified experimental limitations of the original design. During the last quarter of FY08 we redesigned and fabricated a new testing cell to overcome the previous limitations. This cell also offers the capability to test membranes under polarized conditions as well as test the performance of MEAs under selected electrolyzer conditions.

Hobbs, D; Hector Colon-Mercado, H; Mark Elvington, M

2008-09-01T23:59:59.000Z

87

Improvement of Carbon Dioxide Sweep Efficiency by Utilization of Microbial Permeability Profile Modification to Reduce the Amount of Oil Bypassed During Carbon Dioxide Flood  

SciTech Connect

The objective of this project was to couple microbial permeability profile modification (MPPM), with carbon dioxide flooding to improve oil recovery from the Upper Cretaceous Little Creek Oil Field situated in Lincoln and Pike counties, MS. This study determined that MPPM technology, which improves production by utilizing environmentally friendly nutrient solutions to simulate the growth of the indigenous microflora in the most permeable zones of the reservoir thus diverting production to less permeable, previously unswept zones, increased oil production without interfering with the carbon dioxide flooding operation. Laboratory tests determined that no microorganisms were produced in formation waters, but were present in cores. Perhaps the single most significant contribution of this study is the demonstration that microorganisms are active at a formation temperature of 115?C (239?F) by using a specially designed culturing device. Laboratory tests were employed to simulate the MPPM process by demonstrating that microorganisms could be activated with the resulting production of oil in coreflood tests performed in the presence of carbon dioxide at 66?C (the highest temperature that could be employed in the coreflood facility). Geological assessment determined significant heterogeneity in the Eutaw Formation, and documented relatively thin, variably-lithified, well-laminated sandstone interbedded with heavily-bioturbated, clay-rich sandstone and shale. Live core samples of the Upper Cretaceous Eutaw Formation from the Heidelberg Field, MS were quantitatively assessed using SEM, and showed that during MPPM permeability modification occurs ubiquitously within pore and throat spaces of 10-20 ?m diameter. Testing of the MPPM procedure in the Little Creek Field showed a significant increase in production occurred in two of the five production test wells; furthermore, the decline curve in each of the production wells became noticeably less steep. This project greatly extends the number of oil fields in which MPPM can be implemented.

Darrel Schmitz; Lewis Brown F. Leo Lynch; Brenda Kirkland; Krystal Collins; William Funderburk

2010-12-31T23:59:59.000Z

88

Using Vehicle Taxes to Reduce Carbon Dioxide Emissions Rates of New Passenger Vehicles: Evidence from France, Germany, and Sweden  

E-Print Network (OSTI)

France, Germany, and Sweden link vehicle taxes to the carbon dioxide (CO2) emissions rates of passenger vehicles. Based on new vehicle registration data from 2005–2010, a vehicle’s tax is negatively correlated with its ...

Klier, Thomas

89

GLOBAL BIOGEOCHEMICAL CYCLES, VOL. ???, XXXX, DOI:10.1029/, Global Dry Deposition of Nitrogen Dioxide and1  

E-Print Network (OSTI)

-DERIVED NO2 AND SO2 DRY DEPOSITION 1. Introduction Nitrogen dioxide (NO2) and sulfur dioxide (SO2) haveGLOBAL BIOGEOCHEMICAL CYCLES, VOL. ???, XXXX, DOI:10.1029/, Global Dry Deposition of Nitrogen Dioxide and1 Sulfur Dioxide Inferred from Space-Based2 Measurements3 C. R. Nowlan, 1,2 R. V. Martin, 1,2 S

Martin, Randall

90

Advanced byproduct recovery: Direct catalytic reduction of SO{sub 2} to elemental sulfur. First quarterly technical progress report, [October--December 1995  

SciTech Connect

The team of Arthur D. Little, Tufts University and Engelhard Corporation will be conducting Phase I of a four and a half year, two-phase effort to develop and scale-up an advanced byproduct recovery technology that is a direct, single-stage, catalytic process for converting sulfur dioxide to elemental sulfur. this catalytic process reduces SO{sub 2} over a fluorite-type oxide (such as ceria or zirconia). The catalytic activity can be significantly promoted by active transition metals, such as copper. More than 95% elemental sulfur yield, corresponding to almost complete sulfur dioxide conversion, was obtained over a Cu-Ce-O oxide catalyst as part of an ongoing DOE-sponsored University Coal Research Program. This type of mixed metal oxide catalyst has stable activity, high selectivity for sulfur production, and is resistant to water and carbon dioxide poisoning. Tests with CO and CH{sub 4} reducing gases indicates that the catalyst has the potential for flexibility with regard to the composition of the reducing gas, making it attractive for utility use. the performance of the catalyst is consistently good over a range of SO{sub 2} inlet concentration (0.1 to 10%) indicating its flexibility in treating SO{sub 2} tail gases as well as high concentration streams.

Benedek, K. [Little (Arthur D.), Inc., Cambridge, MA (United States); Flytzani-Stephanopoulos, M. [Tufts Univ., Medford, MA (United States)

1996-02-01T23:59:59.000Z

91

Sulfur: its clinical and toxicologic aspects  

Science Journals Connector (OSTI)

Although there is no known dietary requirement for inorganic sulfur, it is an essential element for all animal species in as much as they all require the sulfur-containing amino acid methionine. There are three predominate forms of organic sulfur in animals and humans: 1) the thiomethyl of methionine residues in protein; 2) the sulfhydryl disulfides of protein; and 3) the compounds containing ester or amide bound sulfates of glycosaminoglycans, steroids, and many xenobiotic metabolites. Thus, sulfur becomes an important constituent of amino acids, proteins, enzymes, vitamins and other biomolecules. Unlike mammalian species, plants can use inorganic sulfur and synthesize methionine from which are synthesized all the other important sulfur compounds. Hence, sulfur deficiency occurs mainly when plants are grown in sulfur-depleted soils and when humans and animals consume low-protein diets. In recent times, however, the increasing prevalence of refining petroleum and smelting sulfur compounds of metallic minerals into free metals are having a large impact on the balance of sulfur in the environment. Sulfur toxicity is associated mainly with high levels of the element and its toxic volatile substances in the environment. Sulfur dioxide (SO2), a major air pollutant, may adversely affect animal and human health by causing bronchitis, bronchoconstriction, and increased pulmonary resistance.

Lioudmila A Komarnisky; Robert J Christopherson; Tapan K Basu

2003-01-01T23:59:59.000Z

92

Summary of the presentations at the international workshop on reducing carbon dioxide emissions from the developing world: Assessment of benefits, costs and barriers  

SciTech Connect

The International Workshop on Reducing Carbon Dioxide Emissions from the Developing World: Assessment of Benefits, Costs and Barriers'' was the second workshop held as part of a project being conducted by the International Energy Studies Group of Lawrence Berkeley Laboratory, in collaboration with experts from leading institutions across the developing world. The goal of the project is to analyze long-range energy consumption in developing countries and its potential contribution to global climate change. The US Environmental Protection Agency (EPA) is supporting this work, the results of which already have made a key contribution to the technical analysis being used as the basis for discussion by the Energy and Industry Sub-group of the Intergovernmental Panel on Climate Change (IPCC). The main purpose of this workshop was two-fold: (1) to discuss the feasibility of implementing the efficiency improvements and fuel switching measures incorporated into the long-term energy scenarios created for 17 developing countries and (2) to examine the costs and benefits of reducing energy-related carbon dioxide emissions generated by developing countries.

Sathaye, J.; Goldman, N. (eds.)

1991-06-01T23:59:59.000Z

93

Summary of the presentations at the international workshop on reducing carbon dioxide emissions from the developing world: Assessment of benefits, costs and barriers  

SciTech Connect

The ``International Workshop on Reducing Carbon Dioxide Emissions from the Developing World: Assessment of Benefits, Costs and Barriers`` was the second workshop held as part of a project being conducted by the International Energy Studies Group of Lawrence Berkeley Laboratory, in collaboration with experts from leading institutions across the developing world. The goal of the project is to analyze long-range energy consumption in developing countries and its potential contribution to global climate change. The US Environmental Protection Agency (EPA) is supporting this work, the results of which already have made a key contribution to the technical analysis being used as the basis for discussion by the Energy and Industry Sub-group of the Intergovernmental Panel on Climate Change (IPCC). The main purpose of this workshop was two-fold: (1) to discuss the feasibility of implementing the efficiency improvements and fuel switching measures incorporated into the long-term energy scenarios created for 17 developing countries and (2) to examine the costs and benefits of reducing energy-related carbon dioxide emissions generated by developing countries.

Sathaye, J.; Goldman, N. [eds.

1991-06-01T23:59:59.000Z

94

Two stage sorption of sulfur compounds  

DOE Patents (OSTI)

A two stage method for reducing the sulfur content of exhaust gases is disclosed. Alkali- or alkaline-earth-based sorbent is totally or partially vaporized and introduced into a sulfur-containing gas stream. The activated sorbent can be introduced in the reaction zone or the exhaust gases of a combustor or a gasifier. High efficiencies of sulfur removal can be achieved.

Moore, William E. (Manassas, VA)

1992-01-01T23:59:59.000Z

95

The US department of Energy's R&D program to reduce greenhouse gas emissions through beneficial uses of carbon dioxide  

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

Published in 2011 by John Wiley & Sons, Ltd | Greenhouse Gas Sci Technol. (2011); DOI: 10.1002/ghg Published in 2011 by John Wiley & Sons, Ltd | Greenhouse Gas Sci Technol. (2011); DOI: 10.1002/ghg Perspective Correspondence to: Darin Damiani, National Energy Technology Laboratory, US Department of Energy, 3610 Collins Ferry Road, Morgantown, WV 26507, USA. E-mail: darin.damiani@netl.doe.gov † This article is a US Government work and is in the public domain in the USA. Received June 24, 2011; revised July 26, 2011; accepted July 27, 2011 Published online at Wiley Online Library (wileyonlinelibrary.com) DOI: 10.1002/ghg.35 The US Department of Energy's R&D program to reduce greenhouse gas emissions through benefi cial uses of carbon dioxide † Darin Damiani and John T. Litynski, National Energy Technology Laboratory, US Department of

96

An Analysis of PM and NOx Train Emissions in the Alameda Corridor, CA  

E-Print Network (OSTI)

Environment. Estimation of Nitrogen Dioxide Concentrationsmatter, ozone, nitrogen dioxide and sulfur dioxide - Globalnitrate particles and nitrogen dioxide can reduce visibility

Sangkapichai, Mana; Saphores, Jean-Daniel M; Ritchie, Stephen G.; You, Soyoung Iris; Lee, Gunwoo

2008-01-01T23:59:59.000Z

97

Molecular Dynamics Simulation of Liquid Sulfur Dioxide  

Science Journals Connector (OSTI)

Mauro C. C. Ribeiro * ... Ribeiro, Mauro C. C. ... Marcelo J. Monteiro, Ro?mulo A. Ando, Leonardo J. A. Siqueira, Fernanda F. Camilo, Paulo S. Santos, Mauro C. C. Ribeiro, and Roberto M. Torresi ...

Mauro C. C. Ribeiro

2006-04-11T23:59:59.000Z

98

Intertemporal pricing of sulfur dioxide allowances  

E-Print Network (OSTI)

The Clean Air Act Amendments of 1990 initiated the first large-scale use of the tradable permit approach to pollution control. The theoretical case for this approach rests on the assumption of an efficient market for ...

Bailey, Elizabeth M.

1998-01-01T23:59:59.000Z

99

Reduced  

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Reduced intermittency in the magnetic turbulence of reversed field pinch plasmas L. Marrelli and L. Frassinetti Consorzio RFX, Associazione EURATOM-ENEA sulla Fusione, Corso Stati...

100

Integrated boiler, superheater, and decomposer for sulfuric acid decomposition  

DOE Patents (OSTI)

A method and apparatus, constructed of ceramics and other corrosion resistant materials, for decomposing sulfuric acid into sulfur dioxide, oxygen and water using an integrated boiler, superheater, and decomposer unit comprising a bayonet-type, dual-tube, counter-flow heat exchanger with a catalytic insert and a central baffle to increase recuperation efficiency.

Moore, Robert (Edgewood, NM); Pickard, Paul S. (Albuquerque, NM); Parma, Jr., Edward J. (Albuquerque, NM); Vernon, Milton E. (Albuquerque, NM); Gelbard, Fred (Albuquerque, NM); Lenard, Roger X. (Edgewood, NM)

2010-01-12T23:59:59.000Z

Note: This page contains sample records for the topic "reduce sulfur dioxide" 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

Bisphosphine dioxides  

DOE Patents (OSTI)

A process is described for the production of organic bisphosphine dioxides from organic bisphosphonates. The organic bisphosphonate is reacted with a Grignard reagent to give relatively high yields of the organic bisphosphine dioxide.

Moloy, K.G.

1990-02-20T23:59:59.000Z

102

Performance and cost models for the direct sulfur recovery process. Task 1 Topical report, Volume 3  

SciTech Connect

The purpose of this project is to develop performance and cost models of the Direct Sulfur Recovery Process (DSRP). The DSRP is an emerging technology for sulfur recovery from advanced power generation technologies such as Integrated Gasification Combined Cycle (IGCC) systems. In IGCC systems, sulfur present in the coal is captured by gas cleanup technologies to avoid creating emissions of sulfur dioxide to the atmosphere. The sulfur that is separated from the coal gas stream must be collected. Leading options for dealing with the sulfur include byproduct recovery as either sulfur or sulfuric acid. Sulfur is a preferred byproduct, because it is easier to handle and therefore does not depend as strongly upon the location of potential customers as is the case for sulfuric acid. This report describes the need for new sulfur recovery technologies.

Frey, H.C. [North Carolina State Univ., Raleigh, NC (United States); Williams, R.B. [Carneigie Mellon Univ., Pittsburgh, PA (United States)

1995-09-01T23:59:59.000Z

103

Large Scale U.S. Unconventional Fuels Production and the Role of Carbon Dioxide Capture and Storage Technologies in Reducing Their Greenhouse Gas Emissions  

SciTech Connect

This paper examines the role that carbon dioxide capture and storage technologies could play in reducing greenhouse gas emissions if a significant unconventional fuels industry were to develop within the United States. Specifically, the paper examines the potential emergence of a large scale domestic unconventional fuels industry based on oil shale and coal-to-liquids (CTL) technologies. For both of these domestic heavy hydrocarbon resources, this paper models the growth of domestic production to a capacity of 3 MMB/d by 2050. For the oil shale production case, we model large scale deployment of an in-situ retorting process applied to the Eocene Green River formation of Colorado, Utah, and Wyoming where approximately 75% of the high grade oil shale resources within the United States lies. For the CTL case, we examine a more geographically dispersed coal-based unconventional fuel industry. This paper examines the performance of these industries under two hypothetical climate policies and concludes that even with the wide scale availability of cost effective carbon dioxide capture and storage technologies, these unconventional fuels production industries would be responsible for significant increases in CO2 emissions to the atmosphere. The oil shale production facilities required to produce 3MMB/d would result in net emissions to the atmosphere of between 3000-7000 MtCO2 in addition to storing potentially 1000 to 5000 MtCO2 in regional deep geologic formations in the period up to 2050. A similarly sized domestic CTL industry could result in 4000 to 5000 MtCO2 emitted to the atmosphere in addition to potentially 21,000 to 22,000 MtCO2 stored in regional deep geologic formations over the same period up to 2050. Preliminary analysis of regional CO2 storage capacity in locations where such facilities might be sited indicates that there appears to be sufficient storage capacity, primarily in deep saline formations, to accommodate the CO2 from these industries. However, additional analyses plus detailed regional and site characterization is needed, along with a closer examination of competing storage demands.

Dooley, James J.; Dahowski, Robert T.

2008-11-18T23:59:59.000Z

104

PPPL wins Department of Energy award for reducing greenhouse gases |  

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PPPL wins Department of Energy award for reducing greenhouse gases PPPL wins Department of Energy award for reducing greenhouse gases By Jeanne Jackson DeVoe October 2, 2012 Tweet Widget Facebook Like Google Plus One PPPL engineer Tim Stevenson checks for possible leaks of sulfur hexafluoride (SF6), the gas used to insulate electronic equipment that has the potential to cause global warming at many times the rate of carbon dioxide. PPPL reduced leaks of SF6 by 65 percent over three years - reducing overall greenhouse gas emissions by 48 percent between 2008 and 2011. (Photo by Elle Starkman/PPPL Office of Communications) PPPL engineer Tim Stevenson checks for possible leaks of sulfur hexafluoride (SF6), the gas used to insulate electronic equipment that has the potential to cause global warming at many times the rate of carbon

105

Sulfur minimization in bacterial leaching  

SciTech Connect

The production of sewage biosolids in Ontario in 1989 was estimated to be 7 million m{sup 3} of wet sludge per year. Of this amount, land application accounts for between 20 and 30% of the total. Unfortunately, the use of sewage biosolids on agricultural land is often prohibited because of heavy metal contamination of the biosolids. High cost and operational problems have made chemical methods of metal extraction unattractive. Consequently, microbiological methods of leaching of heavy metals have been studied for over a decade. A relatively simple microbiological process has been investigated in recent years in flask level experiments and recently in a semicontinuous system. The process exploits nonacidophilic and acidophilic indigenous thiobacilli to extract heavy metals from sewage biosolids. These thiobacilli use elemental sulfur as the energy source, producing sulfuric acid. However, the resulting decontaminated biosolids can cause environmental problems like acidification of the soil, when acid is generated from the residual sulfur in the biosolids. The present study examines the possibility of reducing the amount of sulfur added in batch and semicontinuous bacterial leaching systems, and maximizing sulfur oxidation efficiency, thereby reducing the residual sulfur in leached biosolids.

Seth, R.; Prasad, D.; Henry, J.G. [Univ. of Toronto, Ontario (Canada). Dept. of Civil Engineering

1996-11-01T23:59:59.000Z

106

Improve reformer operation with trace sulfur removal  

SciTech Connect

Modern bimetallic reforming catalysts typically have feed specifications for sulfur of 0.5 to 1 wppm in the reformer naphtha carge. Sulfur in the raw naphtha is reduced to this level by naphtha hydrotreating. While most naphtha hydrotreating operations can usually obtain these levels without substantial problems. It is difficult to obtain levels much below 0.5 to 1 wppm with this process. Revamp of a constrained existing hydrotreater to reduce product sulfur slightly can be extremely costly typically entailing replacement or addition of a new reactor. At Engelhard the authors demonstrated that if the last traces of sulfur remaining from hydrotreating can be removed, the resulting ultra-low sulfur feed greatly improves the reformer operation and provides substantial economic benefit to the refiner. Removal of the remaining trace sulfur is accomplished in a simple manner with a special adsorbent bed, without adding complexity to the reforming operation.

McClung, R.G.; Novak, W.J.

1987-01-01T23:59:59.000Z

107

Sonic enhanced ash agglomeration and sulfur capture. Nineteenth quarterly technical progress report, January 3, 1994--March 27, 1994  

SciTech Connect

A major concern with the utilization of coal in directly fired gas turbines is the control of particulate emissions and reduction of sulfur dioxide, and alkali vapor from combustion of coal, up-stream of the gas turbine. Much research and development has been sponsored on methods for particulate emissions control and the direct injection of calcium-based sorbents to reduce SO{sub 2} emission levels. The results of this research and development indicate that both acoustic agglomeration of particulates and direct injection of sorbents have the potential to become a significant emissions control strategy. The Sonic Enhanced Ash Agglomeration and Sulfur Capture program focuses upon the application of an MTCI proprietary invention (Patent No. 5,197,399) for simultaneously enhancing sulfur capture and particulate agglomeration of the combustor effluent. This application can be adapted as either a ``hot flue gas cleanup`` subsystem for the current concepts for combustor islands or as an alternative primary pulse combustor island in which slagging, sulfur capture, particulate agglomeration and control, and alkali gettering as well as NO{sub x} control processes become an integral part of the pulse combustion process. The goal of the program is to support the DOE mission in developing coal-fired combustion gas turbines. In particular, the MTCI proprietary process for bimodal ash agglomeration and simultaneous sulfur capture will be evaluated and developed.

Not Available

1994-07-01T23:59:59.000Z

108

Sulfur meter for blending coal at Plant Monroe: Final report  

SciTech Connect

An on-line sulfur analyzer, installed at the Detroit Edison, Monroe Power station, was placed into service and evaluated for coal blending optimization to minimize the cost of complying with changing stack gas sulfur dioxide regulations. The project involved debugging the system which consisted of an /open quotes/as-fired/close quotes/ sampler and nuclear source sulfur analyzer. The system was initially plagued with mechanical and electronic problems ranging from coal flow pluggages to calibration drifts in the analyzer. Considerable efforts were successfully made to make the system reliable and accurate. On-line testing showed a major improvement in control of sulfur dioxide emission rates and fuel blending optimization equivalent to as much as $6 million in fuel costs at the time of the evaluation. 7 refs., 14 figs., 12 tabs.

Trentacosta, S.D.; Yurko, J.O.

1988-04-01T23:59:59.000Z

109

Graphene-wrapped sulfur nanospheres with ultra-high sulfur loading for high energy density lithium–sulfur batteries  

Science Journals Connector (OSTI)

Abstract Lithium–sulfur (Li–S) battery with high theoretical energy density is one of the most promising energy storage systems for electric vehicles and intermittent renewable energy. However, due to the poor conductivity of the active material, considerable weight of the electrode is occupied by the conductive additives. Here we report a graphene-wrapped sulfur nanospheres composite (S-nanosphere@G) with sulfur content up to 91 wt% as the high energy density cathode material for Li–S battery. The sulfur nanospheres with diameter of 400–500 nm are synthesized through a solution-based approach with the existence of polyvinylpyrrolidone (PVP). Then the sulfur nanospheres are uniformly wrapped by conductive graphene sheets through the electrostatic interaction between graphene oxide and PVP, followed by reducing of graphene oxide with hydrazine. The design of graphene wrapped sulfur nanoarchitecture provides flexible conductive graphene coating with void space to accommodate the volume expansion of sulfur and to minimize polysulfide dissolution. As a result, the S-nanosphere@G nanocomposite with 91 wt% sulfur shows a reversible initial capacity of 970 mA h g?1 and an average columbic efficiency > 96% over 100 cycles at a rate of 0.2 C. Taking the total mass of electrode into account, the S-nanosphere@G composite is a promising cathode material for high energy density Li–S batteries.

Ya Liu; Jinxin Guo; Jun Zhang; Qingmei Su; Gaohui Du

2015-01-01T23:59:59.000Z

110

Offshore Sulfur Comes In  

Science Journals Connector (OSTI)

Offshore Sulfur Comes In ... "The deposit is a major new source of sulfur," say Hines H. Baker, president of Humble Oil, and Langbourne M. Williams, president of Freeport Sulphur. ... Humble's deposit, known as Grand Isle (Block 18), was discovered in the course of offshore oil exploration and it ranks among the most important sulfur discoveries of recent years. ...

1956-10-01T23:59:59.000Z

111

Potential for reducing paper mill energy use and carbon dioxide emissions through plant-wide energy audits: A case study in China  

Science Journals Connector (OSTI)

The pulp and paper industry is one of the most energy-intensive industries worldwide. In 2007, it accounted for 5% of total global industrial energy consumption and 2% of direct industrial carbon dioxide (CO2) emissions. An energy audit is a primary step toward improving energy efficiency at the facility level. This paper describes a plant-wide energy audit aimed at identifying energy conservation and CO2 mitigation opportunities at a paper mill in Guangdong province, China. We describe the energy audit methods, relevant Chinese standards, methods of calculating energy and carbon indicators, baseline energy consumption and CO2 emissions of the audited paper mill, and nine energy-efficiency improvement opportunities identified by the audit. For each of the nine options, we evaluate the energy conservation and associated CO2 mitigation potential. The total technical energy conservation potential for these nine opportunities is 967.8 terajoules (TJ), and the total CO2 mitigation potential is equal to 93,453 tonnes CO2 annually, representing 14.4% and 14.7%, respectively, of the mill’s total energy consumption and CO2 emissions during the audit period.

Lingbo Kong; Lynn Price; Ali Hasanbeigi; Huanbin Liu; Jigeng Li

2013-01-01T23:59:59.000Z

112

Direct determination of organic and inorganic sulfur in coal by controlled oxidation  

SciTech Connect

The overall objective of this project is to develop an analytical method to directly measure the forms of organic sulfur in coal. The method will provide a route to monitor the effectiveness of coal preparation research directed toward removal of organic sulfur in coal. The approach involves subjecting diluted coal samples simultaneously to an oxygen flow and a linear increase in temperature. Distinctive sulfur dioxide evolution patterns are observed among coals of different rank and between raw and treated coals. Assignments have been made relating each specific sulfur dioxide evolution to the non-aromatic organic, aromatic organic, and inorganic sulfur present in coals and treated coals. Work is progressing on schedule to optimize experimental conditions and to improve the efficiency of the controlled-atmosphere programmed-temperature oxidation (CAPTO) method by developing a multiple sample instrumental system.

LaCount, R.B.

1992-01-01T23:59:59.000Z

113

Direct determination of organic and inorganic sulfur in coal by controlled oxidation  

SciTech Connect

The overall objective of this project is to develop an analytical method to directly measure the forms of organic sulfur in coal. The method will provide a route to monitor the effectiveness of coal preparation research directed toward removal of organic sulfur in coal. The approach involves subjecting diluted coal samples simultaneously to an oxygen flow and a linear increase in temperature. Distinctive sulfur dioxide evolution patterns are observed among coals of different rank and between raw and treated coals. Assignments have been made relating each specific sulfur dioxide evolution to the non-aromatic organic, aromatic organic, and inorganic sulfur present in coals and treated coals. Work is progressing on schedule to optimize experimental conditions and to improve the efficiency of the controlled-atmosphere programmed-temperature oxidation (CAPTO) method by developing a multiple sample instrumental system.

LaCount, R.B.

1992-12-31T23:59:59.000Z

114

The reaction kinetics of gasoline sulfur compounds: Catalytic mechanisms for sulfur reduction  

SciTech Connect

One of the key elements of reformulated gasoline is the reduction of the sulfur compounds produced by fluid catalytic cracking. This paper probes the reaction kinetics of refractory gasoline-range thiophene derivatives (thiophene, tetrahydrothiophene, and alkylthiophenes) in an effort to determine the mechanisms of sulfur compound cracking in the FCC unit. The gasoline-range sulfur compounds were analyzed using gas chromatography with an atomic emission detector. The authors` results show that the FCC catalysts affects the cracking of sulfur compounds through both hydrogen transfer and zeolite pore restriction mechanisms. An experimental FCC catalyst is shown to reduce gasoline sulfur content in the Davidson Circulating Riser (DCR{sup TM}) pilot unit. Model compound tests show that the activity of the catalyst is due to both its catalytic and adsorptive properties. Tetrahydrothiophene, which is produced from thiophenes by hydrogen transfer, is completely removed by the experimental catalyst.

Harding, R.H.; Gatte, R.R.; Albro, T.G.; Wormsbecher, R.F. [W.R. Grace & Co. Conn, Columbia, MD (United States)

1993-12-31T23:59:59.000Z

115

ADVANCED BYPRODUCT RECOVERY: DIRECT CATALYTIC REDUCTION OF SO2 TO ELEMENTAL SULFUR  

SciTech Connect

Arthur D. Little, Inc., together with its commercialization partner, Engelhard Corporation, and its university partner Tufts, investigated a single-step process for direct, catalytic reduction of sulfur dioxide from regenerable flue gas desulfurization processes to the more valuable elemental sulfur by-product. This development built on recently demonstrated SO{sub 2}-reduction catalyst performance at Tufts University on a DOE-sponsored program and is, in principle, applicable to processing of regenerator off-gases from all regenerable SO{sub 2}-control processes. In this program, laboratory-scale catalyst optimization work at Tufts was combined with supported catalyst formulation work at Engelhard, bench-scale supported catalyst testing at Arthur D. Little and market assessments, also by Arthur D. Little. Objectives included identification and performance evaluation of a catalyst which is robust and flexible with regard to choice of reducing gas. The catalyst formulation was improved significantly over the course of this work owing to the identification of a number of underlying phenomena that tended to reduce catalyst selectivity. The most promising catalysts discovered in the bench-scale tests at Tufts were transformed into monolith-supported catalysts at Engelhard. These catalyst samples were tested at larger scale at Arthur D. Little, where the laboratory-scale results were confirmed, namely that the catalysts do effectively reduce sulfur dioxide to elemental sulfur when operated under appropriate levels of conversion and in conditions that do not contain too much water or hydrogen. Ways to overcome those limitations were suggested by the laboratory results. Nonetheless, at the end of Phase I, the catalysts did not exhibit the very stringent levels of activity or selectivity that would have permitted ready scale-up to pilot or commercial operation. Therefore, we chose not to pursue Phase II of this work which would have included further bench-scale testing, scale-up, pilot-scale (0.5 MW{sub e}) testing at conditions representative of various regenerable SO{sub 2}-control systems, preparation of a commercial process design, and development of a utility-scale demonstration plan.

Robert S. Weber

1999-05-01T23:59:59.000Z

116

Sulfur@Carbon Cathodes for Lithium Sulfur Batteries > Research...  

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

Electrode Channel Flow DEMS Cell Sulfur@Carbon Cathodes for Lithium Sulfur Batteries Better Ham & Cheese: Enhanced Anodes and Cathodes for Fuel Cells Epitaxial Single...

117

Sulfur-Graphene Oxide Nanocomposite Cathodes for Lithium/Sulfur...  

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

Advanced Materials Advanced Materials Find More Like This Return to Search Sulfur-Graphene Oxide Nanocomposite Cathodes for LithiumSulfur Cells Lawrence Berkeley National...

118

Chapter 11 - Sulfur Recovery  

Science Journals Connector (OSTI)

Abstract Sulfur is present in many raw industrial gases and in natural gas in the form of hydrogen sulfide. Sulfur removal facilities are located at the majority of oil and gas processing facilities throughout the world. The sulfur recovery unit does not make a profit for the operator but it is an essential processing step to allow the overall facility to operate, as the discharge of sulfur compounds to the atmosphere is severely restricted by environmental regulations. Concentration levels of H2S vary significantly depending upon their source. H2S produced from absorption processes, such as amine treating of natural gas or refinery gas, can contain 50–75% H2S by volume or higher. This chapter provides information about fundamentals of sulfur removal facilities in the natural gas industry.

Alireza Bahadori

2014-01-01T23:59:59.000Z

119

Bacterial Sulfur Storage Globules  

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

by I. J. Pickering and G. N. George by I. J. Pickering and G. N. George Sulfur is essential for all life, but it plays a particularly central role in the metabolism of many anaerobic microorganisms. Prominent among these are the sulfide-oxidizing bacteria that oxidize sulfide (S2-) to sulfate (SO42-). Many of these organisms can store elemental sulfur (S0) in "globules" for use when food is in short supply (Fig. 1). The chemical nature of the sulfur in these globules has been an enigma since they were first described as far back as 1887 (1); all known forms (or allotropes) of elemental sulfur are solid at room temperature, but globule sulfur has been described as "liquid", and it apparently has a low density – 1.3 compared to 2.1 for the common yellow allotrope a-sulfur. Various exotic forms of sulfur have been proposed to explain these properties, including micelles (small bubble-like structures) formed from long-chain polythionates, but all of these deductions have been based upon indirect evidence (for example the density was estimated by flotation of intact cells), and many questions remained.

120

HYBRID SULFUR ELECTROLYZER DEVELOPMENT, NHI WORK PACKAGE N-SR07TC0301, FY07 FIRST QUARTER REPORT  

SciTech Connect

The proof of concept of SO2 electrolysis for the hybrid sulfur (HyS) process is the second priority research target of the DOE Nuclear Hydrogen Initiative's thermochemical program for FY07. The proof of concept of the liquid-phase option must be demonstrated at the single cell level for an extended run times (>100 hours). The rate of development of HyS will depend on the identification of a promising membrane or an alternative means for controlling sulfur formation. Once successful long-duration operation has been demonstrated, SRNL will develop a multi-cell stack that can be connected to the H2SO4 decomposer being developed by SNL for the S-I ILS for a Hybrid Sulfur Integrated Laboratory-Scale Experiment during FY 2008. During the first quarter of FY07, SRNL continued the component development and membrane development activities with the goal of identifying and characterizing improved electrodes, electrocatalysts, membranes and MEA configurations which could then be tested at larger scale in the SDE test facility. A modified glass cell was fabricated to allow measurements of sulfur dioxide (SO2) transport across membrane samples at elevated temperatures (up to 70 C). This testing also includes evaluating SO2 transport in different sulfuric acid concentrations (30-70 wt%). A new potentiostat/frequency analyzer was installed for determining ionic conductivity of membranes. This instrument enhances our capabilities to characterize membrane, electrocatalyst and MEA properties and performance. Continuing work from FY06, evaluations were preformed on various commercial and experimental membranes and electrocatalyst materials for the SDE. Several different types of commercially-available membranes were analyzed for sulfur dioxide transport as a function of acid strength including perfluorinated sulfonic acid (PFSA), sulfonated polyetherketone-ketone, and poly-benzimidazole (PBI) membranes. Experimental membranes from the sulfonated diels-alder polyphenylenes (SDAPP) and modified Nafion{reg_sign} 117 were evaluated for SO{sub 2} transport as well. These membranes exhibited reduced transport coefficient for SO{sub 2} transport without the loss in ionic conductivity.

Summers, W

2006-12-20T23:59:59.000Z

Note: This page contains sample records for the topic "reduce sulfur dioxide" 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

Development of the Hybrid Sulfur Thermochemical Cycle  

SciTech Connect

The production of hydrogen via the thermochemical splitting of water is being considered as a primary means for utilizing the heat from advanced nuclear reactors to provide fuel for a hydrogen economy. The Hybrid Sulfur (HyS) Process is one of the baseline candidates identified by the U.S. Department of Energy [1] for this purpose. The HyS Process is a two-step hybrid thermochemical cycle that only involves sulfur, oxygen and hydrogen compounds. Recent work has resulted in an improved process design with a calculated overall thermal efficiency (nuclear heat to hydrogen, higher heating value basis) approaching 50%. Economic analyses indicate that a nuclear hydrogen plant employing the HyS Process in conjunction with an advanced gas-cooled nuclear reactor system can produce hydrogen at competitive prices. Experimental work has begun on the sulfur dioxide depolarized electrolyzer, the major developmental component in the cycle. Proof-of-concept tests have established proton-exchange-membrane cells (a state-of-the-art technology) as a viable approach for conducting this reaction. This is expected to lead to more efficient and economical cell designs than were previously available. Considerable development and scale-up issues remain to be resolved, but the development of a viable commercial-scale HyS Process should be feasible in time to meet the commercialization schedule for Generation IV gas-cooled nuclear reactors.

Summers, William A.; Steimke, John L

2005-09-23T23:59:59.000Z

122

Reduced-Order Model for the Geochemical Impacts of Carbon Dioxide, Brine and Trace Metal Leakage into an Unconfined, Oxidizing Carbonate Aquifer, Version 2.1  

SciTech Connect

The National Risk Assessment Partnership (NRAP) consists of 5 U.S DOE national laboratories collaborating to develop a framework for predicting the risks associated with carbon sequestration. The approach taken by NRAP is to divide the system into components, including injection target reservoirs, wellbores, natural pathways including faults and fractures, groundwater and the atmosphere. Next, develop a detailed, physics and chemistry-based model of each component. Using the results of the detailed models, develop efficient, simplified models, termed reduced order models (ROM) for each component. Finally, integrate the component ROMs into a system model that calculates risk profiles for the site. This report details the development of the Groundwater Geochemistry ROM for the Edwards Aquifer at PNNL. The Groundwater Geochemistry ROM for the Edwards Aquifer uses a Wellbore Leakage ROM developed at LANL as input. The detailed model, using the STOMP simulator, covers a 5x8 km area of the Edwards Aquifer near San Antonio, Texas. The model includes heterogeneous hydraulic properties, and equilibrium, kinetic and sorption reactions between groundwater, leaked CO2 gas, brine, and the aquifer carbonate and clay minerals. Latin Hypercube sampling was used to generate 1024 samples of input parameters. For each of these input samples, the STOMP simulator was used to predict the flux of CO2 to the atmosphere, and the volume, length and width of the aquifer where pH was less than the MCL standard, and TDS, arsenic, cadmium and lead exceeded MCL standards. In order to decouple the Wellbore Leakage ROM from the Groundwater Geochemistry ROM, the response surface was transformed to replace Wellbore Leakage ROM input parameters with instantaneous and cumulative CO2 and brine leakage rates. The most sensitive parameters proved to be the CO2 and brine leakage rates from the well, with equilibrium coefficients for calcite and dolomite, as well as the number of illite and kaolinite sorption sites proving to be of secondary importance. The Groundwater Geochemistry ROM was developed using nonlinear regression to fit the response surface with a quadratic polynomial. The goodness of fit was excellent for the CO2 flux to the atmosphere, and very good for predicting the volumes of groundwater exceeding the pH, TDS, As, Cd and Pb threshold values.

Bacon, Diana H.

2013-03-31T23:59:59.000Z

123

Sulfur Degassing From Volcanoes: Source Conditions, Surveillance, Plume Chemistry and Earth System Impacts  

E-Print Network (OSTI)

of sulfur in magmas owes much to its multiple valence states (-II, 0, IV, VI), speciation (e.g., S2, H2S, SO on the redox chemistry of sulfur: by reducing sulfur, thiosulfate, sulfite and sulfate to H2S, or oxidizing sulfur and H2S to sulfate (e.g., Takano et al. 1997; Amend and Shock 2001; Shock et al. 2010

Boyer, Edmond

124

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

125

China’s Functioning Market for Sulfur Dioxide Scrubbing Technologies  

Science Journals Connector (OSTI)

Department of Geography and Resource Management and Institute of Environment, Energy and Sustainability, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China ... (7, 8) The Roth criteria were proposed to fix broken markets or build new ones if they are missing, which could be especially useful for environmental protection as market failure is often the cause. ...

Yuan Xu

2011-09-29T23:59:59.000Z

126

Supplementary Material Sulfur Dioxide and Primary Carbonaceous Aerosol Emissions  

E-Print Network (OSTI)

(-52%-62%) 14 (-52%-63%) Agricultural waste burning 54 (-86%-120%) 51 (-87%-115%) 52 (-85%-116%) 58 burning 12 (-51%-79%) 19 (-46%-65%) 10 (-52%-99%) 13 (-48%-84%) 12 (-46%-69%) Agricultural waste burning%-64%) 1756 (-37%-66%) 1912 (-38%-65%) Forest & savanna burning 14 (-55%-71%) 23 (-54%-71%) 10 (-56%-72%) 14

Meskhidze, Nicholas

127

Device and method for detecting sulfur dioxide at high temperatures  

DOE Patents (OSTI)

The present invention relates to a method for selectively detecting and/or measuring gaseous SO.sub.2 at a temperature of at least 500.degree. C., the method involving: (i) providing a SO.sub.2-detecting device including an oxygen ion-conducting substrate having on its surface at least three electrodes comprising a first, second, and third electrode; (ii) driving a starting current of specified magnitude and temporal variation between the first and second electrodes; (iii) contacting the SO.sub.2-detecting device with the SO.sub.2-containing sample while maintaining the magnitude and any temporal variation of the starting current, wherein said SO.sub.2-containing sample causes a change in the electrical conductance of said device; and (iv) detecting the change in electrical conductance of the device based on measuring an electrical property related to or indicative of the conductance of the device between the first and third electrodes, or between the second and third electrodes, and detecting SO.sub.2 in the SO.sub.2-containing sample based on the measured change in electrical conductance.

West, David L. (Oak Ridge, TN); Montgomery, Frederick C. (Oak Ridge, TN); Armstrong, Timothy R. (Clinton, TN)

2011-11-01T23:59:59.000Z

128

Impact of Sulfur Dioxide on Lean NOx Trap Catalysts | Department...  

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

Diesel Engine Emissions Reduction (DEER) Conference Presentation: University of New Mexico 2004deerhammache.pdf More Documents & Publications CLEERS Aftertreatment Modeling...

129

Lithium–sulfur batteries: Influence of C-rate, amount of electrolyte and sulfur loading on cycle performance  

Science Journals Connector (OSTI)

Abstract In the past four years major improvement of the lithium sulfur battery technology has been reported. Novel carbon cathode materials offer high sulfur loading, sulfur utilization and cycle stability. An often neglected aspect is that sulfur loading and amount of electrolyte strongly impact the performance. In this paper, we demonstrate how the amount of electrolyte, sulfur loading, lithium excess and cycling rate influences the cycle stability and sulfur utilization. We chose vertically aligned carbon nanotubes (VA-CNT) as model system with a constant areal loading of carbon. For a high reproducibility, decreased weight of current collector and good mechanical adhesion of the VA-CNTs we present a layer transfer technique that enables a light-weight sulfur cathode. The sulfur loading of the cathode was adjusted from 20 to 80 wt.-%. Keeping the total amount of electrolyte constant and varying the C-rate, we are able to demonstrate that the capacity degradation is reduced for high rates, high amount of electrolyte and low sulfur loading. In addition idle periods in the cycling regiment and lower rates result in an increased degradation. We attribute this to the redox-reaction between reactive lithium and polysulfides that correlates with the cycling time, rather than cycle number.

Jan Brückner; Sören Thieme; Hannah Tamara Grossmann; Susanne Dörfler; Holger Althues; Stefan Kaskel

2014-01-01T23:59:59.000Z

130

Nitrogen dioxide detection  

DOE Patents (OSTI)

Method and apparatus for detecting the presence of gaseous nitrogen dioxide and determining the amount of gas which is present. Though polystyrene is normally an insulator, it becomes electrically conductive in the presence of nitrogen dioxide. Conductance or resistance of a polystyrene sensing element is related to the concentration of nitrogen dioxide at the sensing element.

Sinha, Dipen N. (Los Alamos, NM); Agnew, Stephen F. (Los Alamos, NM); Christensen, William H. (Buena Park, CA)

1993-01-01T23:59:59.000Z

131

Freeport Begins Offshore Sulfur Plant  

Science Journals Connector (OSTI)

Freeport Begins Offshore Sulfur Plant ... Discovered by Humble Oil & Refining, the sulfur deposit off Grand Isle is believed by industry observers to be one of the largest discovered in recent years. ...

1958-07-07T23:59:59.000Z

132

SULFUR POLYMER ENCAPSULATION.  

SciTech Connect

Sulfur polymer cement (SPC) is a thermoplastic polymer consisting of 95 wt% elemental sulfur and 5 wt% organic modifiers to enhance long-term durability. SPC was originally developed by the U.S. Bureau of Mines as an alternative to hydraulic cement for construction applications. Previous attempts to use elemental sulfur as a construction material in the chemical industry failed due to premature degradation. These failures were caused by the internal stresses that result from changes in crystalline structure upon cooling of the material. By reacting elemental sulfur with organic polymers, the Bureau of Mines developed a product that successfully suppresses the solid phase transition and significantly improves the stability of the product. SPC, originally named modified sulfur cement, is produced from readily available, inexpensive waste sulfur derived from desulfurization of both flue gases and petroleum. The commercial production of SPC is licensed in the United States by Martin Resources (Odessa, Texas) and is marketed under the trade name Chement 2000. It is sold in granular form and is relatively inexpensive ({approx}$0.10 to 0.12/lb). Application of SPC for the treatment of radioactive, hazardous, and mixed wastes was initially developed and patented by Brookhaven National Laboratory (BNL) in the mid-1980s (Kalb and Colombo, 1985; Colombo et al., 1997). The process was subsequently investigated by the Commission of the European Communities (Van Dalen and Rijpkema, 1989), Idaho National Engineering Laboratory (Darnell, 1991), and Oak Ridge National Laboratory (Mattus and Mattus, 1994). SPC has been used primarily in microencapsulation applications but can also be used for macroencapsulation of waste. SPC microencapsulation has been demonstrated to be an effective treatment for a wide variety of wastes, including incinerator hearth and fly ash; aqueous concentrates such as sulfates, borates, and chlorides; blowdown solutions; soils; and sludges. It is not recommended for treatment of wastes containing high concentrations of nitrates because of potentially dangerous reactions between sulfur, nitrate, and trace quantities of organics. Recently, the process has been adapted for the treatment of liquid elemental mercury and mercury contaminated soil and debris.

KALB, P.

2001-08-22T23:59:59.000Z

133

HYBRID SULFUR ELECTROLYZER DEVELOPMENT FY09 SECOND QUARTER REPORT  

SciTech Connect

The primary objective of the DOE-NE Nuclear Hydrogen Initiative (NHI) is to develop the nuclear hydrogen production technologies necessary to produce hydrogen at a cost competitive with other alternative transportation fuels. The focus of the NHI is on thermochemical cycles and high temperature electrolysis that can be powered by heat from high temperature gas reactors. The Savannah River National Laboratory (SRNL) has been tasked with the primary responsibility to perform research and development in order to characterize, evaluate and develop the Hybrid Sulfur (HyS) thermochemical process. This report documents work during the first quarter of Fiscal Year 2009, for the period between January 1, 2009 and March 31, 2009. The HyS Process is a two-step hybrid thermochemical cycle that is part of the 'Sulfur Family' of cycles. As a sulfur cycle, it uses high temperature thermal decomposition of sulfuric acid to produce oxygen and to regenerate the sulfur dioxide reactant. The second step of the process uses a sulfur dioxide depolarized electrolyzer (SDE) to split water and produce hydrogen by electrochemically reacting sulfur dioxide with H{sub 2}O. The SDE produces sulfuric acid, which is then sent to the acid decomposer to complete the cycle. The DOE NHI program is developing the acid decomposer at Sandia National Laboratory for application to both the HyS Process and the Sulfur Iodine Cycle. The SDE is being developed at SRNL. During FY05 and FY06, SRNL designed and conducted proof-of-concept testing for a SDE using a low temperature, PEM fuel cell-type design concept. The advantages of this design concept include high electrochemical efficiency, small footprint and potential for low capital cost, characteristics that are crucial for successful implementation on a commercial scale. During FY07, SRNL extended the range of testing of the SDE to higher temperature and pressure, conducted a 100-hour longevity test with a 60-cm{sup 2} single cell electrolyzer, and designed and built a larger, multi-cell stack electrolyzer. During FY08, SRNL continued SDE development, including development and successful testing of a three-cell electrolyzer stack with a rated capacity of 100 liters per hour. The HyS program for FY09 program will address improving SDE performance by focusing on preventing or minimizing sulfur deposition inside the cell caused by SO{sub 2} crossover, reduction of cell voltage for improved efficiency, an extension of cell operating lifetime. During FY09 a baseline technology development program is being conducted to address each of these issues. Button-cell (2-cm{sup 2}) and single cell (60-cm{sup 2}) SDEs will be fabricated and tested. A pressurized button-cell test facility will be designed and constructed to facilitate addition testing. The single cell test facility will be upgraded for unattended operation, and later for operation at higher temperature and pressure. Work will continue on development of the Gas Diffusion Electrode (GDE), or Gap Cell, as an alternative electrolyzer design approach that is being developed under subcontract with industry partner Giner Electrochemical Systems. If successful, it could provide an alternative means of preventing sulfur crossover through the proton exchange membrane, as well as the possibility for higher current density operation based on more rapid mass transfer in a gas-phase anode. Promising cell components will be assembled into membrane electrode assemblies (MEAs) and tested in the single cell test facility. Upon modification for unattended operation, test will be conducted for 200 hours or more. Both the button-cell and modified single cell facility will be utilized to demonstrate electrolyzer operation without sulfur build-up limitations, which is a Level 1 Milestone.

Herman, D; David Hobbs, D; Hector Colon-Mercado, H; Timothy Steeper, T; John Steimke, J; Mark Elvington, M

2009-04-15T23:59:59.000Z

134

Why sequence Alkaliphilic sulfur oxidizing bacteria for sulfur pollution  

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

Alkaliphilic sulfur oxidizing Alkaliphilic sulfur oxidizing bacteria for sulfur pollution remediation? Burning sulfur-containing fuels, such as coal, oil, and natural gas, contributes significantly to global environmental problems, such as air pollution and acid rain, besides contributing to the loss of the ozone layer. One method of managing sulfur compounds released as byproducts from industrial processes is to scrub them out using chemical treatments and activated charcoal beds. A lower-cost solution relies on incorporating alkaliphic sulfur-oxidizing bacteria into biofilters to convert the volatile and toxic compounds into insoluble sulfur for easier removal. Discovered in the last decade, these bacteria have been found to thrive in habitats that span the full pH range. The bacteria could have applications

135

Sulfur Dioxide Crossover during the Production of Hydrogen and Sulfuric Acid in a PEM Electrolyzer  

E-Print Network (OSTI)

and must be resup- plied. For example, researchers at the Savannah River National Laboratory SRNL have

Weidner, John W.

136

On the potential economic costs of cutting carbon dioxide emissions in Portugal  

Science Journals Connector (OSTI)

The objective of this paper is to estimate the impact of reducing carbon dioxide emissions from fossil fuel combustion activities on economic ... €6,340. More importantly, and since carbon dioxide emissions are l...

Alfredo Marvão Pereira; Rui Manuel Marvão Pereira

2010-12-01T23:59:59.000Z

137

Viscosity of tetrahydrothiophene-1,1-dioxide  

Science Journals Connector (OSTI)

Substance name(s): tetrahydrothiophene-1,1-dioxide; tetrahydrothiophene-S,S-dioxide; tetrahydro-thiophene-1,1 ... ,1-dioxide; thiacyclopentane dioxide; tetramethylene sulfone; tetrahydrothiophene 1...

Ch. Wohlfarth

2009-01-01T23:59:59.000Z

138

High pressure sulfuric acid decomposition experiments for the sulfur-iodine thermochemical cycle.  

SciTech Connect

A series of three pressurized sulfuric acid decomposition tests were performed to (1) obtain data on the fraction of sulfuric acid catalytically converted to sulfur dioxide, oxygen, and water as a function of temperature and pressure, (2) demonstrate real-time measurements of acid conversion for use as process control, (3) obtain multiple measurements of conversion as a function of temperature within a single experiment, and (4) assess rapid quenching to minimize corrosion of metallic components by undecomposed acid. All four of these objectives were successfully accomplished. This report documents the completion of the NHI milestone on high pressure H{sub 2}SO{sub 4} decomposition tests for the Sulfur-Iodine (SI) thermochemical cycle project. All heated sections of the apparatus, (i.e. the boiler, decomposer, and condenser) were fabricated from Hastelloy C276. A ceramic acid injection tube and a ceramic-sheathed thermocouple were used to minimize corrosion of hot liquid acid on the boiler surfaces. Negligible fracturing of the platinum on zirconia catalyst was observed in the high temperature decomposer. Temperature measurements at the exit of the decomposer and at the entry of the condenser indicated that the hot acid vapors were rapidly quenched from about 400 C to less than 20 C within a 14 cm length of the flow path. Real-time gas flow rate measurements of the decomposition products provided a direct measurement of acid conversion. Pressure in the apparatus was preset by a pressure-relief valve that worked well at controlling the system pressure. However, these valves sometimes underwent abrupt transitions that resulted in rapidly varying gas flow rates with concomitant variations in the acid conversion fraction.

Velasquez, Carlos E; Reay, Andrew R.; Andazola, James C.; Naranjo, Gerald E.; Gelbard, Fred

2005-09-01T23:59:59.000Z

139

Method and system for capturing carbon dioxide and/or sulfur dioxide from gas stream  

DOE Patents (OSTI)

The present invention provides a system for capturing CO.sub.2 and/or SO.sub.2, comprising: (a) a CO.sub.2 and/or SO.sub.2 absorber comprising an amine and/or amino acid salt capable of absorbing the CO.sub.2 and/or SO.sub.2 to produce a CO.sub.2- and/or SO.sub.2-containing solution; (b) an amine regenerator to regenerate the amine and/or amino acid salt; and, when the system captures CO.sub.2, (c) an alkali metal carbonate regenerator comprising an ammonium catalyst capable catalyzing the aqueous alkali metal bicarbonate into the alkali metal carbonate and CO.sub.2 gas. The present invention also provides for a system for capturing SO.sub.2, comprising: (a) a SO.sub.2 absorber comprising aqueous alkali metal carbonate, wherein the alkali metal carbonate is capable of absorbing the SO.sub.2 to produce an alkali metal sulfite/sulfate precipitate and CO.sub.2.

Chang, Shih-Ger; Li, Yang; Zhao, Xinglei

2014-07-08T23:59:59.000Z

140

It's Elemental - The Element Sulfur  

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

Phosphorus Phosphorus Previous Element (Phosphorus) The Periodic Table of Elements Next Element (Chlorine) Chlorine The Element Sulfur [Click for Isotope Data] 16 S Sulfur 32.065 Atomic Number: 16 Atomic Weight: 32.065 Melting Point: 388.36 K (115.21°C or 239.38°F) Boiling Point: 717.75 K (444.60°C or 832.28°F) Density: 2.067 grams per cubic centimeter Phase at Room Temperature: Solid Element Classification: Non-metal Period Number: 3 Group Number: 16 Group Name: Chalcogen What's in a name? From the Sanskrit word sulvere and the Latin word sulphurium. Say what? Sulfur is pronounced as SUL-fer. History and Uses: Sulfur, the tenth most abundant element in the universe, has been known since ancient times. Sometime around 1777, Antoine Lavoisier convinced the rest of the scientific community that sulfur was an element. Sulfur is a

Note: This page contains sample records for the topic "reduce sulfur dioxide" 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

Why sequence purple sulfur bacteria?  

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

purple sulfur bacteria? purple sulfur bacteria? The process by which plants and some bacteria can convert light energy to sugar, or photosynthesis, is crucial to global food webs, and complicated. Very little is known about the photosynthetic bacteria in the purple sulfur bacteria group, which may represent one of the most primitive photosynthetic organisms and are capable of carbon fixation and sequestration in both light and dark conditions with the help of sulfur compounds. Purple sulfur bacteria are autotrophic and can synthesize organic compounds from inorganic sources. Researchers hope to learn more by sequencing nine type strains of purple sulfur bacteria that are found in freshwater, brackish and marine systems. The information would lead to a better understanding of the process of photosynthesis as well as the global

142

Microbial transformations of sulfur compounds  

Science Journals Connector (OSTI)

Oct 13, 1978 ... tains a large part of the chemical energy transferred ... ical energy is partly preserved in the bio- mass of .... ethanol to remove elemental sulfur.

2000-01-10T23:59:59.000Z

143

What's Next for Vanadium Dioxide?  

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

How Atomic Vibrations Transform Vanadium Dioxide How Atomic Vibrations Transform Vanadium Dioxide Calculations Confirm Material's Potential for Next-Generation Electronics, Energy...

144

Carbon Dioxide Capture DOI: 10.1002/anie.201000431  

E-Print Network (OSTI)

Carbon Dioxide Capture DOI: 10.1002/anie.201000431 Carbon Dioxide Capture: Prospects for New] Carbon capture and storage (CCS) schemes embody a group of technologies for the capture of CO2 from power to the atmosphere could be reduced by 80­90% for a modern conventional power plant equipped with carbon capture

145

Carbon dioxide absorbent and method of using the same  

SciTech Connect

In accordance with one aspect, the present invention provides a composition which contains the amino-siloxane structures I, or III, as described herein. The composition is useful for the capture of carbon dioxide from process streams. In addition, the present invention provides methods of preparing the amino-siloxane composition. Another aspect of the present invention provides 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.

Perry, Robert James; O'Brien, Michael Joseph

2014-06-10T23:59:59.000Z

146

Scaling up carbon dioxide capture and storage: From megatons to gigatons Howard J. Herzog  

E-Print Network (OSTI)

Scaling up carbon dioxide capture and storage: From megatons to gigatons Howard J. Herzog MIT Global warming Carbon mitigation Low carbon energy technologies Carbon dioxide capture and storage (CCS) Carbon dioxide (CO2) capture and storage (CCS) is the only technology that can reduce CO2 emissions

147

Clathrate hydrate equilibrium data for the gas mixture of carbon dioxide and nitrogen in the  

E-Print Network (OSTI)

1 Clathrate hydrate equilibrium data for the gas mixture of carbon dioxide and nitrogen the mole fraction of CO2 in the carbon dioxide + nitrogen + cyclopentane mixed hydrate phase, both defined;2 {water +carbon dioxide + nitrogen}, the equilibrium pressure of the mixed hydrate is reduced by 0.95 up

Paris-Sud XI, Université de

148

Reduce Climate Change  

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

Reduce Climate Change Reduce Climate Change Highway vehicles release about 1.5 billion metric tons of greenhouse gases (GHGs) into the atmosphere each year-mostly in the form of carbon dioxide (CO2)-contributing to global climate change. Each gallon of gasoline you burn creates 20 pounds of CO2. That's roughly 5 to 9 tons of CO2 each year for a typical vehicle. more... How can a gallon of gasoline create 20 pounds of carbon dioxide? It seems impossible that a gallon of gasoline, which weighs about 6.3 pounds, could produce 20 pounds of carbon dioxide (CO2) when burned. However, most of the weight of the CO2 doesn't come from the gasoline itself, but the oxygen in the air. When gasoline burns, the carbon and hydrogen separate. The hydrogen combines with oxygen to form water (H2O), and carbon combines with oxygen

149

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

150

HYBRID SULFUR RECOVERY PROCESS FOR NATURAL GAS UPGRADING  

SciTech Connect

This second quarter report of 2002 describes progress on a project funded by the U.S. Department of Energy (DOE) to test a hybrid sulfur recovery process for natural gas upgrading. The process concept represents a low cost option for direct treatment of natural gas streams to remove H{sub 2}S in quantities equivalent to 0.2-25 metric tons (LT) of sulfur per day. This process is projected to have lower capital and operating costs than the competing technologies, amine/aqueous iron liquid redox and amine/Claus/tail gas treating, and have a smaller plant footprint, making it well suited to both on-shore and offshore applications. CrystaSulf (service mark of CrystaTech, Inc.) is a new nonaqueous sulfur recovery process that removes hydrogen sulfide (H{sub 2}S) from gas streams and converts it into elemental sulfur. CrystaSulf features high sulfur recovery similar to aqueous-iron liquid redox sulfur recovery processes, but differs from the aqueous processes in that CrystaSulf controls the location where elemental sulfur particles are formed. In the hybrid process, approximately 1/3 of the total H{sub 2}S in the natural gas is first oxidized to SO{sub 2} at low temperatures over a heterogeneous catalyst. Low temperature oxidation is done so that the H{sub 2}S can be oxidized in the presence of methane and other hydrocarbons without oxidation of the hydrocarbons. The project involves the development of a catalyst using laboratory/bench-scale catalyst testing, and then demonstration of the catalyst at CrystaTech's pilot plant in west Texas. Previous reports described development of a catalyst with the required selectivity and efficiency for producing sulfur dioxide from H{sub 2}S. In the laboratory, the catalyst was shown to be robust and stable in the presence of several intentionally added contaminants, including condensate from the pilot plant site. This report describes testing using the laboratory apparatus but operated at the pilot plant using the actual pilot plant gas, which contains far more contaminants than can be simulated in the laboratory. The results are very encouraging, with stable and efficient operation being obtained for a prolonged period of time.

Girish Srinivas; Steven C. Gebhard; David W. DeBerry

2002-07-01T23:59:59.000Z

151

Conversion of Hydrogen Sulfide in Coal Gases to Liquid Elemental Sulfur with Monolithic Catalysts  

SciTech Connect

Removal of hydrogen sulfide (H{sub 2}S) from coal gasifier gas and sulfur recovery are key steps in the development of Department of Energy's (DOE's) advanced power plants that produce electric power and clean transportation fuels with coal and natural gas. These plants will require highly clean coal gas with H{sub 2}S below 1 ppmv and negligible amounts of trace contaminants such as hydrogen chloride, ammonia, alkali, heavy metals, and particulate. The conventional method of sulfur removal and recovery employing amine, Claus, and tail-gas treatment is very expensive. A second generation approach developed under DOE's sponsorship employs hot-gas desulfurization (HGD) using regenerable metal oxide sorbents followed by Direct Sulfur Recovery Process (DSRP). However, this process sequence does not remove trace contaminants and is targeted primarily towards the development of advanced integrated gasification combined cycle (IGCC) plants that produce electricity (not both electricity and transportation fuels). There is an immediate as well as long-term need for the development of cleanup processes that produce highly clean coal gas for next generation power plants. To this end, a novel process is now under development at several research organizations in which the H{sub 2}S in coal gas is directly oxidized to elemental sulfur over a selective catalyst. Such a process is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S In the Single-Step Sulfur Recovery Process (SSRP), the direct oxidation of H{sub 2}S to elemental sulfur in the presence of SO{sub 2} is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S. This direct oxidation process has the potential to produce a super clean coal gas more economically than both conventional amine-based processes and HGD/DSRP. The H{sub 2} and CO components of syngas appear to behave as inert with respect to sulfur formed at the SSRP conditions. One problem in the SSRP process that needs to be eliminated or minimized is COS formation that may occur due to reaction of CO with sulfur formed from the Claus reaction. The objectives of this research are to formulate monolithic catalysts for removal of H{sub 2}S from coal gases and minimum formation of COS with monolithic catalyst supports, {gamma}-alumina wash coat, and catalytic metals, to develop a regeneration method for a deactivated monolithic catalyst, to measure kinetics of both direct oxidation of H{sub 2}S to elemental sulfur with SO{sub 2} as an oxidizer and formation of COS in the presence of a simulated coal gas mixture containing H{sub 2}, CO, CO{sub 2}, and moisture, using a monolithic catalyst reactor. The task of developing kinetic rate equations and modeling the direct oxidation process to assist in the design of large-scale plants will be abandoned since formulation of catalysts suitable for the removal of H{sub 2}S and COS is being in progress. This heterogeneous catalytic reaction has gaseous reactants such as H{sub 2}S and SO{sub 2}. However, this heterogeneous catalytic reaction has heterogeneous products such as liquid elemental sulfur and steam. Experiments on conversion of hydrogen sulfide into elemental sulfur and formation of COS were carried out for the space time range of 46-570 seconds under reaction conditions to formulate catalysts suitable for the removal of H{sub 2}S and COS from coal gases and evaluate their capabilities in reducing hydrogen sulfide and COS in coal gases. Simulated coal gas mixtures consist of 3,200-4,000-ppmv hydrogen sulfide, 1,600-20,000-ppmv sulfur dioxide, 18-27 v% hydrogen, 29-41 v% CO, 8-12 v% CO{sub 2}, 0-10 vol % moisture, and nitrogen as remainder. Volumetric feed rates of simulated coal gas mixtures to the reactor are 30 - 180 cm{sup 3}/min at 1 atm and 25 C (SCCM). The temperature of the reactor is controlled in an oven at 120-155 C. The pressure of the reactor is maintained at 40-210 psia. The molar ratio

K.C. Kwon

2009-09-30T23:59:59.000Z

152

Carbon dioxide capture under ambient conditions using 2-chloroethylamine  

Science Journals Connector (OSTI)

This is the first case applying 2-haloethylamine to CO2 capture. The prospect of global warming and the urgent need to reduce atmospheric concentration of carbon dioxide has prompted actions at many levels. The c...

Junhua Wang; Xiqin Zhang; Yun Zhou

2011-12-01T23:59:59.000Z

153

Carbon dioxide dissolution in structural and stratigraphic traps  

E-Print Network (OSTI)

The geologic sequestration of carbon dioxide (CO[subscript 2]) in structural and stratigraphic traps is a viable option to reduce anthropogenic emissions. While dissolution of the CO[subscript 2] stored in these traps ...

Hesse, M. A.

154

Graphene-sulfur nanocomposites for rechargeable lithium-sulfur battery electrodes  

SciTech Connect

Rechargeable lithium-sulfur batteries having a cathode that includes a graphene-sulfur nanocomposite can exhibit improved characteristics. The graphene-sulfur nanocomposite can be characterized by graphene sheets with particles of sulfur adsorbed to the graphene sheets. The sulfur particles have an average diameter less than 50 nm..

Liu, Jun; Lemmon, John P; Yang, Zhenguo; Cao, Yuiliang; Li, Xiaolin

2014-06-17T23:59:59.000Z

155

Reducing Diesel Engine Emissions  

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

Reducing Reducing Diesel Engine Emissions 2 0 1 0 Green TransporTaTion TechnoloGies Compared to traditional gasoline engines, diesel engines require less maintenance, generate energy more efficiently, and produce less carbon dioxide emissions. But when uncontrolled, diesel engines churn out harmful emissions like particu- late matter (PM) and nitrogen oxides (NO x ). Researchers at Argonne National Laboratory are currently working to develop

156

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

157

CARBON DIOXIDE EMISSION REDUCTION  

E-Print Network (OSTI)

.5 Primary Energy Use and Carbon Dioxide Emissions for Selected US Chemical Subsectors in 1994 ...............................................................................................................16 Table 2.7 1999 Energy Consumption and Specific Energy Consumption (SEC) in the U.S. Cement Efficiency Technologies and Measures in Cement Industry.................22 Table 2.9 Energy Consumption

Delaware, University of

158

A Mathematical Model for a LithiumSulfur Cell Karthikeyan Kumaresan,a,  

E-Print Network (OSTI)

S8 l is reduced to S2- in steps. For example, S8 l is reduced to S8 2- , then to S6 2- , S4 2- , S2,4 Figure 1 presents a typical experimental discharge profile at a C/50 rate C = 2.5 Ah . The lithium/sulfur Development The schematic of the lithium/sulfur cell modeled in this work is shown in Fig. 2. The cell is made

159

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

160

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

Note: This page contains sample records for the topic "reduce sulfur dioxide" 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

Molecular Structures of Polymer/Sulfur Composites for Lithium...  

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

Structures of PolymerSulfur Composites for Lithium-Sulfur Batteries with Long Cycle Life. Molecular Structures of PolymerSulfur Composites for Lithium-Sulfur Batteries with Long...

162

Amylopectin Wrapped Graphene Oxide/Sulfur for Improved Cyclability of Lithium–Sulfur Battery  

Science Journals Connector (OSTI)

Amylopectin Wrapped Graphene Oxide/Sulfur for Improved Cyclability of Lithium–Sulfur Battery ... An amylopectin wrapped graphene oxide-sulfur composite was prepared to construct a 3-dimensionally cross-linked structure through the interaction between amylopectin and graphene oxide, for stabilizing lithium sulfur batteries. ...

Weidong Zhou; Hao Chen; Yingchao Yu; Deli Wang; Zhiming Cui; Francis J. DiSalvo; Héctor D. Abruña

2013-09-05T23:59:59.000Z

163

Revisit Carbon/Sulfur Composite for Li-S Batteries  

SciTech Connect

To correlate the carbon properties e.g. surface area and porous structure, with the electrochemical behaviors of carbon/sulfur (C/S) composite cathodes for lithium-sulfur (Li-S) batteries, four different carbon frameworks including Ketjen Black (KB, high surface area and porous), Graphene (high surface area and nonporous), Acetylene Black (AB, low surface area and nonporous) and Hollow Carbon Nano Sphere (HCNS, low surface area and porous) are employed to immobilize sulfur (80 wt.%). It has been revealed that high surface area of carbon improves the utilization rate of active sulfur and decreases the real current density during the electrochemical reactions. Accordingly, increased reversible capacities and reduced polarization are observed for high surface area carbon hosts such as KB/S and graphene/S composites. The porous structure of KB or HCNS matrix promotes the long-term cycling stability of C/S composites but only at relatively low rate (0.2 C). Once the current density increases, the pore effect completely disappears and all Li-S batteries show similar trend of capacity degradation regardless of the different carbon hosts used in the cathodes. The reason has been assigned to the formation of reduced amount of irreversible Li2S on the cathode as well as shortened time for polysulfides to transport towards lithium anode at elevated current densities. This work provides valuable information for predictive selection on carbon materials to construct C/S composite for practical applications from the electrochemical point of view.

Zheng, Jianming; Gu, Meng; Wagner, Michael J.; Hays, Kevin; Li, Xiaohong S.; Zuo, Pengjian; Wang, Chong M.; Zhang, Jiguang; Liu, Jun; Xiao, Jie

2013-07-23T23:59:59.000Z

164

The Net Environmental Effects of Carbon Dioxide Reduction Policies  

E-Print Network (OSTI)

of policy measures have been proposed to reduce the emissions of carbon dioxide (CO2). However, policies which reduce CO2 emissions will also decrease the emissions of greenhouse-relevant gases methane are overlooked the net effect of CO2 reduction policies on global warming is understated. Thus, emissions of all

165

CARBON DIOXIDE FIXATION.  

SciTech Connect

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

166

Refractive index of tetrahydrothiophene-1,1-dioxide  

Science Journals Connector (OSTI)

Substance name(s): tetrahydrothiophene-1,1-dioxide; tetrahydrothiophene-S,S-dioxide; tetrahydro-thiophene-1,1 ... ,1-dioxide; thiacyclopentane dioxide; tetramethylene sulfone; tetrahydrothiophene 1...

Ch. Wohlfarth

2008-01-01T23:59:59.000Z

167

Dielectric constant of tetrahydrothiophene-1,1-dioxide  

Science Journals Connector (OSTI)

Substance name(s): tetrahydrothiophene-1,1-dioxide; tetrahydrothiophene-S,S-dioxide; tetrahydro-thiophene-1,1 ... ,1-dioxide; thiacyclopentane dioxide; tetramethylene sulfone; tetrahydrothiophene 1...

Ch. Wohlfarth

2008-01-01T23:59:59.000Z

168

Direct sulfur recovery during sorbent regeneration. Final report  

SciTech Connect

The objective of this research project was to improve the direct elemental sulfur yields that occur during the regeneration of SO{sub 2}-saturated MgO-vermiculite sorbents (MagSorbents) by examining three approaches or strategies. The three approaches were regeneration-gas recycle, high-pressure regeneration, and catalytic reduction of the SO{sub 2} gas using a new catalyst developed by Research Triangle Institute (RTI). Prior to the project, Sorbent Technologies Corporation (Sorbtech) had developed a sorbent-regeneration process that yielded directly a pure elemental sulfur product. In the process, typically about 25 to 35 percent of the liberated S0{sub 2} was converted directly to elemental sulfur. The goal of this project was to achieve a conversion rate of over 90 percent. Good success was attained in the project. About 90 percent or more conversion was achieved with two of the approaches that were examined, regeneration-gas recycle and use of the RTI catalyst. Of these approaches, regeneration-gas recycle gave the best results (essentially 100 percent conversion in some cases). In the regeneration-gas recycle approach, saturated sorbent is simply heated to about 750{degree}C in a reducing gas (methane) atmosphere. During heating, a gas containing elemental sulfur, water vapor, H{sub 2}S, S0{sub 2}, and C0{sub 2} is evolved. The elemental sulfur and water vapor in the gas stream are condensed and removed, and the remaining gas is recycled back through the sorbent bed. After several recycles, the S0{sub 2} and H{sub 2}S completely disappear from the gas stream, and the stream contains only elemental sulfur, water vapor and C0{sub 2}.

Nelson, S.G.; Little, R.C. [Sorbent Technologies Corp., Twinsburg, OH (United States)

1993-08-01T23:59:59.000Z

169

Sulfur geochemistry of thermogenic gas hydrate and associated sediment from the Texas-Louisiana continental slope  

E-Print Network (OSTI)

total reduced sulfide (TRS), acid volatile sulfide, and citrate-dithionate and HCl extractable iron. Pore-fluid measurements included []H?S, chloride, sulfate, ammonia and total dissolved inorganic carbon. Gas hydrate hydrogen sulfide and carbon dioxide...

Gledhill, Dwight Kuehl

2001-01-01T23:59:59.000Z

170

The use of ethanol to remove sulfur from coal. Final report, September 1991--December 1992; Revision  

SciTech Connect

The initial technical goal in the project was to develop a chemical method for the cost effective removal of both inorganic and organic sulfur from Ohio coals. Verifying and using a process of reacting ethanol vapors with coal under conditions disclosed in U.S. Patent 4,888,029, the immediate technical objectives were to convert a small scale laborative batch process to a larger scale continuous process which can serve as the basis for commercial development of the technology. This involved getting as much information as possible from small scale batch autoclave or fluid bed laboratory reactors for use in pilot plant studies. The laboratory data included material balances on the coal and sulfur, temperature and pressure ranges for the reaction, minimum reaction times at different conditions, the effectiveness of different activators such as oxygen and nitric oxide, the amount and nature of by-products such as sulfur dioxide, hydrogen sulfide and acetaldehyde, the effect of coal particle size on the speed and completeness of the reaction, and the effectiveness of the reaction on different Ohio coals. Because the laboratory experiments using the method disclosed in U.S. 4,888,029 were not successful, the objective for the project was changed to develop a new laboratory process to use ethanol to remove sulfur from coal. Using copper as a catalyst and as an H{sub 2}S scavenger, a new laboratory procedure to use ethanol to remove sulfur from coal has been developed at Ohio University and a patent application covering this process was filed in March, 1993. The process is based on the use of copper as a catalyst for the dehydrogenation of ethanol to produce nascent hydrogen to remove sulfur from the coal and the use of copper as a scavenger to capture the hydrogen sulfide formed from the sulfur removed from coal.

Savage, R.L.; Lazarov, L.K.; Prudich, M.E.; Lange, C.A.; Kumar, N.

1994-03-10T23:59:59.000Z

171

The complete genome sequence of Staphylothermus marinus reveals differences in sulfur metabolism among heterotrophic Crenarchaeota  

SciTech Connect

Staphylothermus marinus is an anaerobic, sulfur-reducing peptide fermenter of the archaeal phylum Crenarchaeota. It is the third heterotrophic, obligate sulfur reducing crenarchaeote to be sequenced and provides an opportunity for comparative analysis of the three genomes. The 1.57 Mbp genome of the hyperthermophilic crenarchaeote Staphylothermus marinus has been completely sequenced. The main energy generating pathways likely involve 2-oxoacid:ferredoxin oxidoreductases and ADP-forming acetyl-CoA synthases. S. marinus possesses several enzymes not present in other crenarchaeotes including a sodium ion-translocating decarboxylase likely to be involved in amino acid degradation. S. marinus lacks sulfur-reducing enzymes present in the other two sulfur-reducing crenarchaeotes that have been sequenced - Thermofilum pendens and Hyperthermus butylicus. Instead it has three operons similar to the mbh and mbx operons of Pyrococcus furiosus, which may play a role in sulfur reduction and/or hydrogen production. The two marine organisms, S. marinus and H. butylicus, possess more sodium-dependent transporters than T. pendens and use symporters for potassium uptake while T. pendens uses an ATP-dependent potassium transporter. T. pendens has adapted to a nutrient-rich environment while H. butylicus is adapted to a nutrient-poor environment, and S. marinus lies between these two extremes. The three heterotrophic sulfur-reducing crenarchaeotes have adapted to their habitats, terrestrial vs. marine, via their transporter content, and they have also adapted to environments with differing levels of nutrients. Despite the fact that they all use sulfur as an electron acceptor, they are likely to have different pathways for sulfur reduction.

Anderson, iain J.; Dharmarajan, Lakshmi; Rodriguez, Jason; Hooper, Sean; Porat, Iris; Ulrich, Luke E.; Elkins, James G.; Mavromatis, Kostas; Sun, Hui; Land, Miriam; Lapidus, Alla; Lucas, Susan; Barry, Kerrie; Huber, Harald; Zhulin, Igor B.; Whitman, William B.; Mukhopadhyay, Biswarup; Woese, Carl; Bristow, James; Kyrpides, Nikos

2008-09-05T23:59:59.000Z

172

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 Novomer’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.

173

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

174

Impact of Light-Duty Vehicle Emissions on 21st Century Carbon Dioxide Concentrations  

SciTech Connect

The impact of light-duty passenger vehicle emissions on global carbon dioxide concentrations was estimated using the MAGICC reduced-form climate model combined with the PNNL contribution to the CCSP scenarios product. Our central estimate is that tailpipe light duty vehicle emissions of carbon-dioxide over the 21st century will increase global carbon dioxide concentrations by slightly over 12 ppmv by 2100.

Smith, Steven J.; Kyle, G. Page

2007-08-04T23:59:59.000Z

175

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

176

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

177

The Viscosity of Carbon Dioxide  

Science Journals Connector (OSTI)

26 July 1912 research-article The Viscosity of Carbon Dioxide P. Phillips The Royal Society is collaborating with JSTOR to digitize, preserve, and extend access to Proceedings...

1912-01-01T23:59:59.000Z

178

Photosynthesis and carbon dioxide fixation  

Science Journals Connector (OSTI)

Photosynthesis and carbon dioxide fixation ... Photosynthetic pigments, photosystems, the Calvin cycle, the Hatch-Slack pathway, photorespiration, and photosynthetic yield improvement. ...

Muriel B. Bishop; Carl B. Bishop

1987-01-01T23:59:59.000Z

179

High-temperature sorbent method for removal of sulfur containing gases from gaseous mixtures  

DOE Patents (OSTI)

A copper oxide-zinc oxide mixture is used as a sorbent for removing hydrogen sulfide and other sulfur containing gases at high temperatures from a gaseous fuel mixture. This high-temperature sorbent is especially useful for preparing fuel gases for high temperature fuel cells. The copper oxide is initially reduced in a preconditioning step to elemental copper and is present in a highly dispersed state throughout the zinc oxide which serves as a support as well as adding to the sulfur sorption capacity. The spent sorbent is regenerated by high-temperature treatment with an air fuel, air steam mixture followed by hydrogen reduction to remove and recover the sulfur.

Young, John E. (Woodridge, IL); Jalan, Vinod M. (Concord, MA)

1984-01-01T23:59:59.000Z

180

High-temperature sorbent method for removal of sulfur-containing gases from gaseous mixtures  

DOE Patents (OSTI)

A copper oxide-zinc oxide mixture is used as a sorbent for removing hydrogen sulfide and other sulfur containing gases at high temperatures from a gaseous fuel mixture. This high-temperature sorbent is especially useful for preparing fuel gases for high temperature fuel cells. The copper oxide is initially reduced in a preconditioning step to elemental copper and is present in a highly dispersed state throughout the zinc oxide which serves as a support as well as adding to the sulfur sorbtion capacity. The spent sorbent is regenerated by high-temperature treatment with an air fuel, air steam mixture followed by hydrogen reduction to remove and recover the sulfur.

Young, J.E.; Jalan, V.M.

1982-07-07T23:59:59.000Z

Note: This page contains sample records for the topic "reduce sulfur dioxide" 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

High-temperature sorbent method for removal of sulfur containing gases from gaseous mixtures  

DOE Patents (OSTI)

A copper oxide-zinc oxide mixture is used as a sorbent for removing hydrogen sulfide and other sulfur containing gases at high temperatures from a gaseous fuel mixture. This high-temperature sorbent is especially useful for preparing fuel gases for high temperature fuel cells. The copper oxide is initially reduced in a preconditioning step to elemental copper and is present in a highly dispersed state throughout the zinc oxide which serves as a support as well as adding to the sulfur sorption capacity. The spent sorbent is regenerated by high-temperature treatment with an air fuel, air steam mixture followed by hydrogen reduction to remove and recover the sulfur.

Young, J.E.; Jalan, V.M.

1984-06-19T23:59:59.000Z

182

Method of making sulfur-resistant composite metal membranes  

DOE Patents (OSTI)

The invention provides thin, hydrogen-permeable, sulfur-resistant membranes formed from palladium or palladium-alloy coatings on porous, ceramic or metal supports. Also disclosed are methods of making these membranes via sequential electroless plating techniques, wherein the method of making the membrane includes decomposing any organic ligands present on the substrate, reducing the palladium crystallites on the substrate to reduced palladium crystallites, depositing a film of palladium metal on the substrate and then depositing a second, gold film on the palladium film. These two metal films are then annealed at a temperature between about 200.degree. C. and about 1200.degree. C. to form a sulfur-resistant, composite PdAu alloy membrane.

Way, J. Douglas (Boulder, CO) [Boulder, CO; Lusk, Mark (Golden, CO) [Golden, CO; Thoen, Paul (Littleton, CO) [Littleton, CO

2012-01-24T23:59:59.000Z

183

HYBRID SULFUR RECOVERY PROCESS FOR NATURAL GAS UPGRADING  

SciTech Connect

This final report describes the objectives, technical approach, results and conclusions for a project funded by the U.S. Department of Energy to test a hybrid sulfur recovery process for natural gas upgrading. The process concept is a configuration of CrystaTech, Inc.'s CrystaSulf{reg_sign} process which utilizes a direct oxidation catalyst upstream of the absorber tower to oxidize a portion of the inlet hydrogen sulfide (H{sub 2}S) to sulfur dioxide (SO{sub 2}) and elemental sulfur. This hybrid configuration of CrystaSulf has been named CrystaSulf-DO and represents a low-cost option for direct treatment of natural gas streams to remove H{sub 2}S in quantities equivalent to 0.2-25 metric tons (LT) of sulfur per day and more. This hybrid process is projected to have lower capital and operating costs than the competing technologies, amine/aqueous iron liquid redox and amine/Claus/tail gas treating, and have a smaller plant footprint, making it well suited to both onshore and offshore applications. CrystaSulf is a nonaqueous sulfur recovery process that removes H{sub 2}S from gas streams and converts it to elemental sulfur. In CrystaSulf, H{sub 2}S in the inlet gas is reacted with SO{sub 2} to make elemental sulfur according to the liquid phase Claus reaction: 2H{sub 2}S + SO{sub 2} {yields} 2H{sub 2}O + 3S. The SO{sub 2} for the reaction can be supplied from external sources by purchasing liquid SO{sub 2} and injecting it into the CrystaSulf solution, or produced internally by converting a portion of the inlet gas H{sub 2}S to SO{sub 2} or by burning a portion of the sulfur produced to make SO{sub 2}. CrystaSulf features high sulfur recovery similar to aqueous-iron liquid redox sulfur recovery processes, but differs from the aqueous processes in that CrystaSulf controls the location where elemental sulfur particles are formed. In the hybrid process, the needed SO{sub 2} is produced by placing a bed of direct oxidation catalyst in the inlet gas stream to oxidize a portion of the inlet H{sub 2}S. Oxidation catalysts may also produce some elemental sulfur under these conditions, which can be removed and recovered prior to the CrystaSulf absorber. The CrystaSulf-DO process can utilize direct oxidation catalyst from many sources. Numerous direct oxidation catalysts are available from many suppliers worldwide. They have been used for H{sub 2}S oxidation to sulfur and/or SO{sub 2} for decades. It was believed at the outset of the project that TDA Research, Inc., a subcontractor, could develop a direct oxidation catalyst that would offer advantages over other commercially available catalysts for this CrystaSulf-DO process application. This project involved the development of several of TDA's candidate proprietary direct oxidation catalysts through laboratory bench-scale testing. These catalysts were shown to be effective for conversion of H{sub 2}S to SO{sub 2} and to elemental sulfur under certain operating conditions. One of these catalysts was subsequently tested on a commercial gas stream in a bench-scale reactor at CrystaTech's pilot plant site in west Texas with good results. However, commercial developments have precluded the use of TDA catalysts in the CrystaSulf-DO process. Nonetheless, this project has advanced direct oxidation catalyst technology for H{sub 2}S control in energy industries and led to several viable paths to commercialization. TDA is commercializing the use of its direct oxidation catalyst technology in conjunction with the SulfaTreat{reg_sign} solid scavenger for natural gas applications and in conjunction with ConocoPhillips and DOE for gasification applications using ConocoPhillips gasification technology. CrystaTech is commercializing its CrystaSulf-DO process in conjunction with Gas Technology Institute for natural gas applications (using direct oxidation catalysts from other commercial sources) and in conjunction with ChevronTexaco and DOE for gasification applications using ChevronTexaco's gasification technology.

Dennis Dalrymple

2004-06-01T23:59:59.000Z

184

Carbon dioxide capture and geological storage  

Science Journals Connector (OSTI)

...Blundell and Fraser Armstrong Carbon dioxide capture and geological storage Sam...Nottingham NG12 5GG, UK Carbon dioxide capture and geological storage is a...80-90%. It involves the capture of carbon dioxide at a large industrial...

2007-01-01T23:59:59.000Z

185

Flue gas carbon dioxide sequestration during water softening with ion-exchange fibers  

SciTech Connect

This study examines the use of ion-exchange fibers (IX fibers) to permanently sequester carbon dioxide present in flue gas into an aqueous phase as calcium or magnesium alkalinity while concurrently softening hard water. The only process inputs besides carbon dioxide (or flue gas) are snowmelt (or rainwater); no other chemicals are required for the regeneration of the IX fibers. Importantly, the process is not energy intensive and carbon dioxide does not need to be compressed to excessive pressures (>150 psi) for efficient use. Sources of carbon dioxide do not require concentration and, therefore, the use of raw flue gas (similar to 17% CO{sub 2}) is feasible with the rate of sequestration governed only by the partial pressure of carbon dioxide. While valid for flue gas obtained from any combustion process (e.g., coal, oil, natural gas, etc.), emissions from oil or gas combustion may be more appropriate for use in the described process due to the absence of mercury and particulates. It should also be noted that the presence of sulfur dioxide in flue gas would not adversely affect the process and may even enhance regeneration efficiency. The only product of the proposed process is an environmentally benign regenerant stream containing calcium and/or magnesium alkalinity. The unique property of IX fibers that makes the proposed process both environmentally sustainable and economically feasible is amenability to efficient regeneration with carbon dioxide and harvested snowmelt. Low intraparticle diffusional resistance is the underlying reason why IX fibers are amenable to efficient regeneration using snowmelt sparged with carbon dioxide; 95% calcium recovery was attained at a CO{sub 2} partial pressure of 6.8 atm. The energy balance for a typical electric utility shows that up to 1% of carbon dioxide emitted during combustion would be sequestered in the softening process.

Greenleaf, J.E.; SenGupta, A.K. [Lafayette College, Easton, PA (United States). Dept. of Civil & Environmental Engineering

2009-06-15T23:59:59.000Z

186

Enhanced electrochemical performance by wrapping graphene on carbon nanotube/sulfur composites for rechargeable lithium–sulfur batteries  

Science Journals Connector (OSTI)

Abstract A novel graphene-wrapped carbon nanotube/sulfur structure was designed to improve the electrochemical performance of the lithium–sulfur (Li–S) batteries. Owing to the introduction of the reduced graphene oxide (rGO) with the aim to restrain the polysulfide anions diffusion phenomenon, increase the overall electronic conductivity of the electrode and accommodate volume expansion between the delithiated S and lithiated Li2S phases, the resulted graphene-wrapped carbon nanotube/sulfur (S/CNT@rGO) composite makes the cycling performance of the Li–S batteries better than that without rGO. The S/CNT@rGO composite showed an initial discharge capacity of ~1299 mA h g?1 at 0.2 C rate. After 100 cycles of charge/discharge, the S/CNT@rGO composite retained a high specific capacity of ~670 mA h g?1, much higher than that without rGO (graphene-wrapped carbon nanotube/sulfur composite could be a promising cathode material for high-rate performance Li–S batteries.

Yishan Wu; Chunmei Xu; Jinxin Guo; Qingmei Su; Gaohui Du; Jun Zhang

2014-01-01T23:59:59.000Z

187

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.

Not Available

1990-10-01T23:59:59.000Z

188

Dynamic reduced order modeling of entrained flow gasifiers  

E-Print Network (OSTI)

Gasification-based energy systems coupled with carbon dioxide capture and storage technologies have the potential to reduce greenhouse gas emissions from continued use of abundant and secure fossil fuels. Dynamic reduced ...

Monaghan, Rory F. D. (Rory Francis Desmond)

2010-01-01T23:59:59.000Z

189

Carbon Dioxide Sequestration in Concrete Using Vacuum-Carbonation Alain Azar, Prof. Yixin Shao  

E-Print Network (OSTI)

Carbon Dioxide Sequestration in Concrete Using Vacuum-Carbonation Alain Azar, Prof. Yixin Shao promising carbon uptake results and is a viable option for carbonation curing. Carbon sequestration increase in Carbon dioxide (CO2) emissions over the past five decades, specific ways to reduce

Barthelat, Francois

190

Carbon/Sulfur Nanocomposites and Additives for High-Energy Lithium...  

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

CarbonSulfur Nanocomposites and Additives for High-Energy Lithium Sulfur Batteries CarbonSulfur Nanocomposites and Additives for High-Energy Lithium Sulfur Batteries 2011 DOE...

191

The Cost of Carbon Dioxide Capture and Storage in Geologic Formations  

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

CosT of Carbon DioxiDe CapTure CosT of Carbon DioxiDe CapTure anD sTorage in geologiC formaTions The sequestration of carbon dioxide (CO 2 ) in geologic formations is a viable option for achieving deep reductions in greenhouse gas emissions without hindering economic prosperity. Due to the abundance of fossil fuels in the United States and around the globe as compared to other energy sources, there is strong interest in geologic sequestration, but cost is a key issue. The volume of CO 2 emitted from power plants and other energy systems is enormous compared to other emissions of concern. For example, a pulverized coal (PC) boiler operating on Illinois #6 coal (2.5 percent sulfur) may generate 0.03 pounds of sulfur dioxide per kilowatt hour (kWh) and emit CO 2 at a rate of 1.7 pounds per kWh.

192

HYDROCARBON AND SULFUR SENSORS FOR SOFC SYSTEMS  

SciTech Connect

The following report summarizes work conducted during the Phase I program Hydrocarbon and Sulfur Sensors for SOFC Systems under contract No. DE-FC26-02NT41576. For the SOFC application, sensors are required to monitor hydrocarbons and sulfur in order to increase the operation life of SOFC components. This report discusses the development of two such sensors, one based on thick film approach for sulfur monitoring and the second galvanic based for hydrocarbon monitoring.

A.M. Azad; Chris Holt; Todd Lesousky; Scott Swartz

2003-11-01T23:59:59.000Z

193

Sulfur-Free Selective Pulping  

E-Print Network (OSTI)

Technoeconomic Appraisal," December 1991. 5. DOE Annual Report on Contract No. AC02-83CH10093, Bozell, J. J., Hames, B., Chum, H. L., Dimmel, D. R, Althen, E., Caldwell, P. L., Daube, Oxidation ;; Diels-Alder .. I I -Methanol .. ~ 5 I 3 (C~O) OCH... - Hydrogen 3 (Q-IP) # Q-I 3 o o ~ o 1 2 ~ (H) Lignin DMBQ =two OCH3 groups Anthraquinone MMBQ =one OCH3 group A. K, and Kuroda, K-I.,"Sulfur-free Selective Pulping," March 1992. 6. DOE Annual Report on Contrac No. DE-AC02-83CH10093, Bozell, J. J...

Dimmel, D. R.; Bozell, J. J.

194

THE EFFECT OF ANOLYTE PRODUCT ACID CONCENTRATION ON HYBRID SULFUR CYCLE PERFORMANCE  

SciTech Connect

The Hybrid Sulfur (HyS) cycle (Fig. 1) is one of the simplest, all-fluids thermochemical cycles that has been devised for splitting water with a high-temperature nuclear or solar heat source. It was originally patented by Brecher and Wu in 1975 and extensively developed by Westinghouse in the late 1970s and early 1980s. As its name suggests, the only element used besides hydrogen and oxygen is sulfur, which is cycled between the +4 and +6 oxidation states. HyS comprises two steps. One is the thermochemical (>800 C) decomposition of sulfuric acid (H{sub 2}SO{sub 4}) to sulfur dioxide (SO{sub 2}), oxygen (O{sub 2}), and water. H{sub 2}SO{sub 4} = SO{sub 2} + 1/2 O{sub 2} + H{sub 2}O. The other is the SO{sub 2}-depolarized electrolysis of water to H{sub 2}SO{sub 4} and hydrogen (H{sub 2}), SO{sub 2} + 2 H{sub 2}O = H{sub 2}SO{sub 4} + H{sub 2}, E{sup o} = -0.156 V, explaining the 'hybrid' designation. These two steps taken together split water into H{sub 2} and O{sub 2} using heat and electricity. Researchers at the Savannah River National Laboratory (SRNL) and at the University of South Carolina (USC) have successfully demonstrated the use of proton exchange membrane (PEM) electrolyzers (Fig. 2) for the SO{sub 2}-depolarized electrolysis (sulfur oxidation) step, while Sandia National Laboratories (SNL) successfully demonstrated the high-temperature sulfuric acid decomposition (sulfur reduction) step using a bayonet-type reactor (Fig. 3). This latter work was performed as part of the Sulfur-Iodine (SI) cycle Integrated Laboratory Scale demonstration at General Atomics (GA). The combination of these two operations results in a simple process that will be more efficient and cost-effective for the massive production of hydrogen than alkaline electrolysis. Recent developments suggest that the use of PEMs other than Nafion will allow sulfuric acid to be produced at higher concentrations (>60 wt%), offering the possibility of net thermal efficiencies around 50% (HHV basis). The effect of operation at higher anolyte concentrations on the flowsheet, and on the net thermal efficiency for a nuclear-heated HyS process, is examined and quantified.

Gorensek, M.; Summers, W.

2010-03-24T23:59:59.000Z

195

Sulfurization of a carbon surface for vapor phase mercury removal II: Sulfur forms and mercury uptake  

E-Print Network (OSTI)

promote the formation of organic sulfur and the presence of H2S during the cooling process increased in the presence of H2S was very effective towards Hg uptake in nitrogen. Corre- lation of mercury uptake capacitySulfurization of a carbon surface for vapor phase mercury removal ­ II: Sulfur forms and mercury

Borguet, Eric

196

Sorbent utilization prediction methodology: sulfur control in fluidized-bed combustors  

SciTech Connect

The United States Government has embarked on an ambitious program to develop and commercialize technologies to efficiently extract energy from coal in an environmentally acceptable manner. One of the more promising new technologies for steam and power generation is the fluidized-bed combustion of coal. In this process, coal is burned in a fluidized bed composed mainly of calcined limestone sorbent. The calcium oxide reacts chemically to capture the sulfur dioxide formed during the combustion and to maintain the stack gas sulfur emissions at acceptable levels. The spent sulfur sorbent, containing calcium sulfate, is a dry solid that can be disposed of along with coal ash or potentially used. Other major advantages of fluidized-bed combustion are the reduction in nitrogen oxide emissions because of the relatively low combustion temperatures, the capability of burning wide varieties of fuel, the high carbon combustion efficiencies, and the high heat-transfer coefficients. A key to the widespread commercialization of fluidized-bed technology is the ability to accurately predict the amount of sulfur that will be captured by a given sorbent. This handbook meets this need by providing a simple, yet reliable, user-oriented methodology (the ANL method) that allows performance of a sorbent to be predicted. The methodology is based on only three essential sorbent parameters, each of which can be readily obtained from standardized laboratory tests. These standard tests and the subsequent method of data reduction are described in detail.

Fee, D.C.; Wilson, W.I.; Shearer, J.A.; Smith, G.W.; Lenc, J.F.; Fan, L.S.; Myles, K.M.; Johnson, I.

1980-09-01T23:59:59.000Z

197

Impact of the Presence of Carbon Monoxide and Carbon Dioxide on Gas Oil Hydrotreatment: Investigation on Liquids from Biomass Cotreatment with Petroleum Cuts  

Science Journals Connector (OSTI)

Impact of the Presence of Carbon Monoxide and Carbon Dioxide on Gas Oil Hydrotreatment: Investigation on Liquids from Biomass Cotreatment with Petroleum Cuts ... A potential way of utilizing these bioliquids as fuels could be the direct hydrotreatment(6) or the cohydrotreatment with petroleum fractions,(7) such as atmospheric gas oils, to achieve the technical and environmental fuel standards, especially in terms of sulfur content. ...

Ana Pinheiro; Nathalie Dupassieux; Damien Hudebine; Christophe Geantet

2011-01-18T23:59:59.000Z

198

Cost-cutting for offshore sulfur recovery processes studied  

SciTech Connect

An increasing portion of future US gas supply is likely to come from offshore, primarily Gulf of Mexico. Because this gas can be sour, the industry has sought lower cost H{sub 2}S-removal/recovery processes for treating it. Usually the gas contains < 5 tons/day (tpd) of sulfur. A study to compare several emerging sulfur-removal/recovery processes against a baseline Amine/LO-CAT II process has indicated that some emerging processes, though not yet commercialized, show considerable potential for reducing costs. Specifically, the major findings were that Double Loop and CrystaSulf, developed by Radian International LLC, Austin, were the least expensive capital-cost processes by a significant margin and that Marathon Oil Co.`s Hysulf`s cost has the potential to compete with Double Loop and CrystaSulf.

Quinlan, M.P.; Echterhoff, L.W. [M.W. Kellogg Co., Houston, TX (United States); Leppin, D.; Meyer, H.S. [Gas Research Inst., Chicago, IL (United States)

1997-07-21T23:59:59.000Z

199

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

E-Print Network (OSTI)

Carbon Dioxide Sequestration Industrial-scale processes are available for separating carbon dioxide dioxide separation and sequestration because the lower cost of carbon dioxide separation from for injection of carbon dioxide into oil or gas-bearing formations. An advantage of sequestration involving

200

High-Sulfur Coal for Generating Electricity  

Science Journals Connector (OSTI)

High-Sulfur...FLUIDIZED-BED COMBUSTORS, COMBUSTION...MAY FLUE GAS DES S E...1971 ). High-sulfur...was brief. Natural gas became...overdependent on natural gas and oil to...elevated pressure with a downward...coals of high ash-fusion...

James T. Dunham; Carl Rampacek; T. A. Henrie

1974-04-19T23:59:59.000Z

Note: This page contains sample records for the topic "reduce sulfur dioxide" 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

A decomposition analysis of carbon dioxide emissions in the Chinese nonferrous metal industry  

Science Journals Connector (OSTI)

The nonferrous metal industry (NMI) of China consumes large amounts of energy and associated emissions of carbon dioxide (CO 2) are very high. Actions to reduce CO 2 emissions and ener...

Y. Shi; T. Zhao

2014-11-01T23:59:59.000Z

202

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-

203

Recuperative supercritical carbon dioxide cycle  

DOE Patents (OSTI)

A power plant includes a closed loop, supercritical carbon dioxide system (CLS-CO.sub.2 system). The CLS-CO.sub.2 system includes a turbine-generator and a high temperature recuperator (HTR) that is arranged to receive expanded carbon dioxide from the turbine-generator. The HTR includes a plurality of heat exchangers that define respective heat exchange areas. At least two of the heat exchangers have different heat exchange areas.

Sonwane, Chandrashekhar; Sprouse, Kenneth M; Subbaraman, Ganesan; O'Connor, George M; Johnson, Gregory A

2014-11-18T23:59:59.000Z

204

HYBRID SULFUR PROCESS REFERENCE DESIGN AND COST ANALYSIS  

SciTech Connect

This report documents a detailed study to determine the expected efficiency and product costs for producing hydrogen via water-splitting using energy from an advanced nuclear reactor. It was determined that the overall efficiency from nuclear heat to hydrogen is high, and the cost of hydrogen is competitive under a high energy cost scenario. It would require over 40% more nuclear energy to generate an equivalent amount of hydrogen using conventional water-cooled nuclear reactors combined with water electrolysis compared to the proposed plant design described herein. There is a great deal of interest worldwide in reducing dependence on fossil fuels, while also minimizing the impact of the energy sector on global climate change. One potential opportunity to contribute to this effort is to replace the use of fossil fuels for hydrogen production by the use of water-splitting powered by nuclear energy. Hydrogen production is required for fertilizer (e.g. ammonia) production, oil refining, synfuels production, and other important industrial applications. It is typically produced by reacting natural gas, naphtha or coal with steam, which consumes significant amounts of energy and produces carbon dioxide as a byproduct. In the future, hydrogen could also be used as a transportation fuel, replacing petroleum. New processes are being developed that would permit hydrogen to be produced from water using only heat or a combination of heat and electricity produced by advanced, high temperature nuclear reactors. The U.S. Department of Energy (DOE) is developing these processes under a program known as the Nuclear Hydrogen Initiative (NHI). The Republic of South Africa (RSA) also is interested in developing advanced high temperature nuclear reactors and related chemical processes that could produce hydrogen fuel via water-splitting. This report focuses on the analysis of a nuclear hydrogen production system that combines the Pebble Bed Modular Reactor (PBMR), under development by PBMR (Pty.) Ltd. in the RSA, with the Hybrid Sulfur (HyS) Process, under development by the Savannah River National Laboratory (SRNL) in the US as part of the NHI. This work was performed by SRNL, Westinghouse Electric Company, Shaw, PBMR (Pty) Ltd., and Technology Insights under a Technical Consulting Agreement (TCA). Westinghouse Electric, serving as the lead for the PBMR process heat application team, established a cost-shared TCA with SRNL to prepare an updated HyS thermochemical water-splitting process flowsheet, a nuclear hydrogen plant preconceptual design and a cost estimate, including the cost of hydrogen production. SRNL was funded by DOE under the NHI program, and the Westinghouse team was self-funded. The results of this work are presented in this Final Report. Appendices have been attached to provide a detailed source of information in order to document the work under the TCA contract.

Gorensek, M.; Summers, W.; Boltrunis, C.; Lahoda, E.; Allen, D.; Greyvenstein, R.

2009-05-12T23:59:59.000Z

205

Method of removal of sulfur from coal and petroleum products  

DOE Patents (OSTI)

A method for the removal of sulfur from sulfur-bearing materials such as coal and petroleum products using organophosphine and organophosphite compounds is provided.

Verkade, John G. (Ames, IA); Mohan, Thyagarajan (Ames, IA); Angelici, Robert J. (Ames, IA)

1995-01-01T23:59:59.000Z

206

Investigation of Sulfur Deactivation on Cu/Zeolite SCR Catalysts...  

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

of Sulfur Deactivation on CuZeolite SCR Catalysts in Diesel Application Investigation of Sulfur Deactivation on CuZeolite SCR Catalysts in Diesel Application Investigation of...

207

Additives and Cathode Materials for High-Energy Lithium Sulfur...  

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

Additives and Cathode Materials for High-Energy Lithium Sulfur Batteries Additives and Cathode Materials for High-Energy Lithium Sulfur Batteries 2013 DOE Hydrogen and Fuel Cells...

208

Manipulating the Surface Reactions in Lithium Sulfur Batteries...  

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

Manipulating the Surface Reactions in Lithium Sulfur Batteries Using Hybrid Anode Structures. Manipulating the Surface Reactions in Lithium Sulfur Batteries Using Hybrid Anode...

209

Sulfur nanocrystals anchored graphene composite with highly improved electrochemical performance for lithium–sulfur batteries  

Science Journals Connector (OSTI)

Abstract Two kinds of graphene–sulfur composites with 50 wt% of sulfur are prepared using hydrothermal method and thermal mixing, respectively. Transmission Electron Microscopy (TEM) and Energy Dispersive X-ray Spectra mapping show that sulfur nanocrystals with size of ?5 nm dispersed on graphene sheets homogeneously for the sample prepared by hydrothermal method (NanoS@G). While for the thermal mixed graphene–sulfur composite (S–G mixture), sulfur shows larger and uneven size (50–200 nm). X-ray Photoelectron Spectra (XPS) reveals the strong chemical bonding between the sulfur nanocrystals and graphene. Comparing with the S–G mixture, the NanoS@G composite shows highly improved electrochemical performance as cathode for lithium–sulfur (Li–S) battery. The NanoS@G composite delivers an initial capacity of 1400 mAh g?1 with the sulfur utilization of 83.7% at a current density of 335 mA g?1. The capacity keeps above 720 mAh g?1 over 100 cycles. The strong adherence of the sulfur nanocrystals on graphene immobilizes sulfur and polysulfides species and suppressed the “shuttle effect”, resulting higher coulombic efficiency and better capacity retention. Electrochemical impedance also suggests that the strong bonding enabled rapid electronic/ionic transport and improved electrochemical kinetics, therefore good rate capability is obtained. These results demonstrate that the NanoS@G composite is a very promising candidate for high-performance Li–S batteries.

Jun Zhang; Zimin Dong; Xiuli Wang; Xuyang Zhao; Jiangping Tu; Qingmei Su; Gaohui Du

2014-01-01T23:59:59.000Z

210

Innovative Carbon Dioxide Sequestration from Flue Gas Using an In-Duct Scrubber Coupled with Alkaline Clay Mineralization  

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

Innovative Carbon Dioxide Sequestration Innovative Carbon Dioxide Sequestration from Flue Gas Using an In-Duct Scrubber Coupled with Alkaline Clay Mineralization Background The United States Department of Energy (DOE) is leading an effort to find novel approaches to reduce carbon dioxide (CO 2 ) emissions from industrial sources. The Industrial Carbon Capture and Sequestration (ICCS) program is funded by the American Recovery and Reinvestment Act (ARRA) to encourage development of processes that

211

Sulfur-graphene oxide material for lithium-sulfur battery cathodes  

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

Sulfur-graphene oxide material for lithium-sulfur battery cathodes Sulfur-graphene oxide material for lithium-sulfur battery cathodes Theoretical specific energy and theoretical energy density Scanning electron micrograph of the GO-S nanocomposite June 2013 Searching for a safer, less expensive alternative to today's lithium-ion batteries, scientists have turned to lithium-sulfur as a possible chemistry for next-generation batteries. Li/S batteries have several times the energy storage capacity of the best currently available rechargeable Li-ion battery, and sulfur is inexpensive and nontoxic. Current batteries using this chemistry, however, suffer from extremely short cycle life-they don't last through many charge-discharge cycles before they fail. A research team led by Elton Cairns and Yuegang Zhang has developed a new

212

Removal of sulfur and nitrogen containing pollutants from discharge gases  

DOE Patents (OSTI)

Oxides of sulfur and of nitrogen are removed from waste gases by reaction with an unsupported copper oxide powder to form copper sulfate. The resulting copper sulfate is dissolved in water to effect separation from insoluble mineral ash and dried to form solid copper sulfate pentahydrate. This solid sulfate is thermally decomposed to finely divided copper oxide powder with high specific surface area. The copper oxide powder is recycled into contact with the waste gases requiring cleanup. A reducing gas can be introduced to convert the oxide of nitrogen pollutants to nitrogen.

Joubert, James I. (Pittsburgh, PA)

1986-01-01T23:59:59.000Z

213

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

214

Phosphazene groups modified sulfur composites as active cathode materials for rechargeable lithium/sulfur batteries  

Science Journals Connector (OSTI)

A novel phosphazene groups modified sulfur composites cathode [triphosphazene sulfide composite (PS) or nitroaniline–triphosphazene disulfide composite (NPS)] which can give good affinity with electrolytes was...

J. D. Liu; S. Q. Zhang; S. B. Yang; Z. F. Shi; S. T. Zhang; L. K. Wu

2013-11-01T23:59:59.000Z

215

Energy Levels in Sulfur Nuclei  

Science Journals Connector (OSTI)

A study has been made of the proton groups from the reaction of 3.22-Mev deuterons with sulfur in the form, primarily, of H2S gas. The following Q values have been assigned to the reaction S32(dp)S33:6.48, 5.69, 4.58, 4.31, 3.63, 3.33, 2.60, 2.33, 2.06, 1.78, 1.37, 0.85, and 0.18 Mev, corresponding to the ground state and twelve excited states of S33. Four of these groups have been investigated for proton gamma-ray coincidences to confirm this assignment. The yield as a function of deuteron energy has been observed for the six highest energy groups and indication of the presence of some broad resonances found. A qualitative measurement of the variation with angle of relative yields of the groups has indicated a proton intensity distribution that is symmetric for some groups and asymmetric for others. The cross section for the reaction for 90° observation has been found to be 1.2 barns. The mass difference S33-S32 has been calculated to be 0.99963 mass unit.Two low intensity, high energy groups have been assigned to the reaction S33(dp)S34 with Q values of 8.67 and 7.85 Mev. This, together with the above observation, leads to a value of 1.99691 for the mass difference S34-S32.

Perry W. Davison

1949-03-01T23:59:59.000Z

216

Carbon Dioxide: Threat or Opportunity?  

E-Print Network (OSTI)

tion will be by direct combustion for the generation of power, but an increasing proportion will be con verted to syngas for chemical and fuel uses. Coal gasification is projected to become a major industry in the next decade. For every ton of coal... entering the gasification process, 1.88 lons of carbon dio xide are produced. This carbon dioxide is removed in virtually pure form by existing technology. This same technology can be applied to remove carbon dioxide from stack gases produced by power...

McKinney, A. R.

1982-01-01T23:59:59.000Z

217

Steam reforming utilizing sulfur tolerant catalyst  

SciTech Connect

This patent describes a steam reforming process for converting hydrocarbon material to hydrogen gas in the presence of sulfur which consists of: adding steam to the hydrocarbon material and passing the steam and hydrocarbon material over catalyst material at elevated temperatures. The improvement comprises utilizing as a catalyst material high activity, sulfur tolerant catalyst of platinum supported on lanthanum stabilized alumina or magnesium promoted lanthanum stabilized alumina. It also describes a steam process for converting hydrocarbon material to hydrogen gas in the presence of sulfur which consists of steam to the hydrocarbon material over catalyst material at elevated temperatures. The improvement comprises utilizing as a catalyst material high activity, sulfur tolerant catalysts consisting essentially of iridium supported on lanthanum stabilized alumina or magnesium promoted lanthanum stabilized alumina. In addition a steam reforming process is described for converting hydrocarbon material to hydrogen gas in the presence of sulfur comprising adding steam to the hydrocarbon material and passing the steam and hydrocarbon material over catalyst material at elevated temperatures. The improvement comprises utilizing as a catalyst material high activity sulfur tolerant catalysts consisting essentially of palladium supported on lanthanum stabilized alumina or magnesium promoted lanthanum stabilized alumina.

Setzer, H.J.; Karavolis, S.; Bett, J.A.S.

1987-09-15T23:59:59.000Z

218

Capture of carbon dioxide from ambient air  

Science Journals Connector (OSTI)

Carbon dioxide capture from ambient air could compensate for all carbon dioxide emissions to the atmosphere. Such capture would, for example, make it possible to use liquid, carbon-based fuels in cars or airplane...

K.S. Lackner

2009-09-01T23:59:59.000Z

219

Carbon Dioxide and Methane Emissions from Estuaries  

Science Journals Connector (OSTI)

Carbon dioxide and methane emissions from estuaries are reviewed in relation with biogeochemical processes and carbon cycling. In estuaries, carbon dioxide and methane emissions show a large spatial and temporal ...

Gwenaël Abril; Alberto Vieira Borges

2005-01-01T23:59:59.000Z

220

FIELD DEMONSTRATION OF CARBON DIOXIDE MISCIBLE FLOODING IN THE LANSING-KANSAS CITY FORMATION, CENTRAL KANSAS  

SciTech Connect

A pilot carbon dioxide miscible flood was initiated in the Lansing Kansas City C formation in the Hall Gurney Field, Russell County, Kansas. Continuous carbon dioxide injection began on December 2, 2003. By the end of December 2004, 11.39 MM lb of carbon dioxide were injected into the pilot area. Carbon dioxide injection rates averaged about 242 MCFD. Vent losses were excessive during June as ambient temperatures increased. Installation of smaller plungers in the carbon dioxide injection pump reduced the recycle and vent loss substantially. Carbon dioxide was detected in one production well near the end of May and in the second production well in August. No channeling of carbon dioxide was observed. The GOR has remained within the range of 3000-4000 for most the last six months. Wells in the pilot area produced 100% water at the beginning of the flood. Oil production began in February, increasing to an average of about 2.35 B/D for the six month period between July 1 and December 31. Cumulative oil production was 814 bbls. Neither well has experienced increased oil production rates expected from the arrival of the oil bank generated by carbon dioxide injection.

Alan Byrnes; G. Paul Willhite; Don Green; Martin Dubois; Richard Pancake; Timothy Carr; W. Lynn Watney; John Doveton; Willard Guy; Rodney Reynolds; Dave Murfn; James Daniels; Russell Martin; William Flanders; Dave Vander Griend; Eric Mork; Paul Cantrell

2004-12-31T23:59:59.000Z

Note: This page contains sample records for the topic "reduce sulfur dioxide" 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

FISCAL YEAR 2006 REPORT ON ELECTROLYZER COMPONENT DEVELOPMENT FOR THE HYBRID SULFUR PROJECT  

SciTech Connect

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. In FY05, testing at the Savannah River National Laboratory (SRNL) explored a low temperature fuel cell design concept for the SDE. The advantages of this design concept include high electrochemical efficiency and small volumetric footprint that is crucial for successful implementation on a commercial scale. A key component of the SDE is the ion conductive membrane through which protons produced at anode migrate to the cathode and react to produce hydrogen. An ideal membrane for the SDE should have both low ionic resistivity and low sulfur dioxide transport. These features allow the electrolyzer to perform at high currents with low potentials, along with preventing contamination of both the hydrogen output and poisoning of the catalysts involved. Another key component is the electrocatalyst material used for the anode and cathode. Good electrocatalysts should be chemically stable and low overpotential for the desired electrochemical reactions. This report summarizes results from activities to evaluate different membrane and electrocatalyst materials for the SDE. Several different types of commercially-available membranes were analyzed for ionic resistance and sulfur dioxide transport including perfluorinated sulfonic acid, sulfonated poly-etherketone-ketone, and poly-benzimidazole membranes. Of these membrane types, the poly-benzimidazole (PBI) membrane, Celtec-L, exhibited the best combination of characteristics for use in an SDE. Testing examined the activity and stability of platinum and palladium as 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 concentration of the sulfuric acid. Various cell configurations were examined with respect to the deposition of electrocatalyst and use of conductive carbon materials such as carbon cloth and carbon paper. Findings from these evaluations and the results of the membrane and electrocatalyst testing, we prepared three different membrane electrode assemblies (MEA) for electrolyzer testing. The first MEA consisted of a Nafion{reg_sign} membrane with platinum electrocatalyst deposited on carbon cloths, which were heat pressed onto the membrane, an assembly identical to those used in proton exchange membrane fuel cells. The second MEA also used a Nafion membrane with the electrocatalysts deposited directly onto the membrane. The third MEA proved similar to the second but utilized a PBI membrane in place of the Nafion{reg_sign} membrane. Tailor of the membrane and catalysts properties for the SDE system was concluded as a required step for the technology to move forward. It was also recommended the evaluation of the tested and new developed materials at conditions closer to the SDE operating conditions and for longer period of time.

Colon-Mercado, H; David Hobbs, D; Daryl Coleman, D; Amy Ekechukwu, A

2006-08-03T23:59:59.000Z

222

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 of technologies developed to capture carbon dioxide (Co2) gas from the exhausts of power stations and from other

223

Condenser-type diffusion denuders for the collection of sulfur dioxide in a cleanroom  

Science Journals Connector (OSTI)

High-efficiency condenser-type diffusion denuders of cylindrical and planar geometries are described. The film condensation of water vapor onto a cooled denuder surface can be used as a method for collecting w...

In-Hyoung Chang; Dong Soo Lee; Soon-Ho Ock

2003-02-01T23:59:59.000Z

224

The excited state geometry associated with the 2900A absorption spectrum of sulfur dioxide  

E-Print Network (OSTI)

Za in Eqs. [18], [19], and [ZO], and the ground state vibrational frequencies Vl" and VZ" in Eq. [16]. Once the L" matrix has been determined, the normal coordi- nates ql" and qZ" could be obtained by the transformation [24] written for the ground... vs. log E for any plate or film has the form shown in Figure l. a b Log Exposure Figure l. Optical density vs. log exposure for a film or plate. Note that over the range (a, b) the graph is practically linear, We may also write Eq. I 2...

Smith, David Robert, Jr

2012-06-07T23:59:59.000Z

225

Wave lengths of some new absorption bands of sulfur dioxide vapor  

E-Print Network (OSTI)

is made in two sections with flanges on each end to permit, bolting the sections and end plates together. One en/, the left in figure 3, is equipped with two pair of adjusting screws which are used to change the orientation of two half mirrors, mounted... in figure 4, was based on two objectives. One was getting the maximum amount of light through the system and to the photographic plate. This was a major problem because the light rays become quite weak after being re- flected many times by the mirrors...

Landrum, Bobby Lee

2012-06-07T23:59:59.000Z

226

Quantitative application of the Franck-Condon theory to sulfur dioxide  

E-Print Network (OSTI)

there are N(G^) molecules In the absorbing path. Since the absorption 2J. H. Clements, Phys. Rev. 47. 220 (1935). ^F. Almassy and H. Laemmel, Helv. Chlm. Acta. 33, 2092, (1950). ^G. B. Kistiakowski and A. H. Solomon, JN Chem. Phys. 1, 609 (1937). 2... there are N(G^) molecules In the absorbing path. Since the absorption 2J. H. Clements, Phys. Rev. 47. 220 (1935). ^F. Almassy and H. Laemmel, Helv. Chlm. Acta. 33, 2092, (1950). ^G. B. Kistiakowski and A. H. Solomon, JN Chem. Phys. 1, 609 (1937). 2...

Coffman, Moody Lee

2013-10-04T23:59:59.000Z

227

Organoclay Sorbent for Removal of Carbon Dioxide from Gas Streams at Low Temperatures  

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

Organoclay Sorbent for Removal of Carbon Dioxide from Gas Organoclay Sorbent for Removal of Carbon Dioxide from Gas Streams at Low Temperatures Contact NETL Technology Transfer Group techtransfer@netl.doe.gov October 2012 Significance * Energy mixing is maximized * Mobilizing of the particulates is complete * No "dead zones" exist * Packing of material is minimized * Eroding effects are significantly reduced Applications * Mixing nuclear waste at Hanford * Any similar industrial process involving heavy solids in a carrier fluid Opportunity Research is currently active on the patent-pending technology "Organoclay Sorbent for Removal of Carbon Dioxide from

228

Carbon/Sulfur Nanocomposites and Additives for High-Energy Lithium...  

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

& Publications Additives and Cathode Materials for High-Energy Lithium Sulfur Batteries CarbonSulfur Nanocomposites and Additives for High-Energy Lithium Sulfur Batteries...

229

An Aerosol Condensation Model for Sulfur Trioxide  

SciTech Connect

This document describes a model for condensation of sulfuric acid aerosol given an initial concentration and/or source of gaseous sulfur trioxide (e.g. fuming from oleum). The model includes the thermochemical effects on aerosol condensation and air parcel buoyancy. Condensation is assumed to occur heterogeneously onto a preexisting background aerosol distribution. The model development is both a revisiting of research initially presented at the Fall 2001 American Geophysical Union Meeting [1] and a further extension to provide new capabilities for current atmospheric dispersion modeling efforts [2]. Sulfuric acid is one of the most widely used of all industrial chemicals. In 1992, world consumption of sulfuric acid was 145 million metric tons, with 42.4 Mt (mega-tons) consumed in the United States [10]. In 2001, of 37.5 Mt consumed in the U.S., 74% went into producing phosphate fertilizers [11]. Another significant use is in mining industries. Lawuyi and Fingas [7] estimate that, in 1996, 68% of use was for fertilizers and 5.8% was for mining. They note that H{sub 2}SO{sub 4} use has been and should continue to be very stable. In the United States, the elimination of MTBE (methyl tertiary-butyl ether) and the use of ethanol for gasoline production are further increasing the demand for petroleum alkylate. Alkylate producers have a choice of either a hydrofluoric acid or sulfuric acid process. Both processes are widely used today. Concerns, however, over the safety or potential regulation of hydrofluoric acid are likely to result in most of the growth being for the sulfuric acid process, further increasing demand [11]. The implication of sulfuric acid being a pervasive industrial chemical is that transport is also pervasive. Often, this is in the form of oleum tankers, having around 30% free sulfur trioxide. Although sulfuric acid itself is not a volatile substance, fuming sulfuric acid (referred to as oleum) is [7], the volatile product being sulfur trioxide. Sulfate aerosols and mist may form in the atmosphere on tank rupture. From chemical spill data from 1990-1996, Lawuyi02 and Fingas [7] prioritize sulfuric acid as sixth most serious. During this period, they note 155 spills totaling 13 Mt, out of a supply volume of 3700 Mt. Lawuyi and Fingas [7] summarize information on three major sulfuric acid spills. On 12 February 1984, 93 tons of sulfuric acid were spilled when 14 railroad cars derailed near MacTier, Parry Sound, Ontario. On 13 December 1978, 51 railroad cars derailed near Springhill, Nova Scotia. One car, containing 93% sulfuric acid, ruptured, spilling nearly its entire contents. In July 1993, 20 to 50 tons of fuming sulfuric acid spilled at the General Chemical Corp. plant in Richmond, California, a major industrial center near San Francisco. The release occurred when oleum was being loaded into a nonfuming acid railroad tank car that contained only a rupture disk as a safety device. The tank car was overheated and this rupture disk blew. The resulting cloud of sulfuric acid drifted northeast with prevailing winds over a number of populated areas. More than 3,000 people subsequently sought medical attention for burning eyes, coughing, headaches, and nausea. Almost all were treated and released on the day of the spill. By the day after the release, another 5,000 people had sought medical attention. The spill forced the closure of five freeways in the region as well as some Bay Area Rapid Transit System stations. Apart from corrosive toxicity, there is the additional hazard that the reactions of sulfur trioxide and sulfuric acid vapors with water are extremely exothermic [10, 11]. While the vapors are intrinsically denser than air, there is thus the likelihood of strong, warming-induced buoyancy from reactions with ambient water vapor, water-containing aerosol droplets, and wet environmental surface. Nordin [12] relates just such an occurrence following the Richmond, CA spill, with the plume observed to rise to 300 m. For all practical purposes, sulfur trioxide was the constituent released from the heated tank

Grant, K E

2008-02-07T23:59:59.000Z

230

Electrochemical separation and concentration of sulfur containing gases from gas mixtures  

DOE Patents (OSTI)

A method of removing sulfur oxides of H.sub.2 S from high temperature gas mixtures (150.degree.-1000.degree. C.) is the subject of the present invention. An electrochemical cell is employed. The cell is provided with inert electrodes and an electrolyte which will provide anions compatible with the sulfur containing anions formed at the anode. The electrolyte is also selected to provide inert stable cations at the temperatures encountered. The gas mixture is passed by the cathode where the sulfur gases are converted to SO.sub.4.sup.= or, in the case of H.sub.2 S, to S.sup.=. The anions migrate to the anode where they are converted to a stable gaseous form at much greater concentration levels (>10X). Current flow may be effected by utilizing an external source of electrical energy or by passing a reducing gas such as hydrogen past the anode.

Winnick, Jack (3805 Woodrail-on-the-Green, Columbia, MO 65201)

1981-01-01T23:59:59.000Z

231

Reduced viscosity  

Science Journals Connector (OSTI)

n. (1) (IUPAC: viscosity number) Reduced viscosity is the fluid viscosity increase per unit of polymer solute concentration.... where ? ...

2007-01-01T23:59:59.000Z

232

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

233

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

234

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.

235

Safety considerations for the use of sulfur in sulfur-modified pavement materials  

E-Print Network (OSTI)

on the surround1ng environment. As sulfur-modified paving materials were being developed, there was a corresponding concern for studying the amounts of gaseous emiss1ons that were generated. The Texas Trans- portat1on Inst1tute (TTI) was one of the first... organizations in the United States to become 1nvolved in the research and development of sulfur-modified pavements, Throughout 1ts laboratory stud1es TTI cont1nually mon1tored hydrogen sulf1de (H25) and sulfur d1oxide (502) em1ssions produced during mix...

Jacobs, Carolyn Yuriko

2012-06-07T23:59:59.000Z

236

Dielectric constant of the mixture (1) tetrahydrothiophene-1,1-dioxide; (2) pyridine  

Science Journals Connector (OSTI)

Substance name(s): tetrahydrothiophene-1,1-dioxide; tetrahydrothiophene-S,S-dioxide; tetrahydro-thiophene-1,1 ... ,1-dioxide; thiacyclopentane dioxide; tetramethylene sulfone; tetrahydrothiophene 1...

Ch. Wohlfarth

2008-01-01T23:59:59.000Z

237

Viscosity of the mixture (1) tetrahydrothiophene-1,1-dioxide; (2) ethylbenzene  

Science Journals Connector (OSTI)

Substance name(s): tetrahydrothiophene-1,1-dioxide; tetrahydrothiophene-S,S-dioxide; tetrahydro-thiophene-1,1 ... ,1-dioxide; thiacyclopentane dioxide; tetramethylene sulfone; tetrahydrothiophene 1...

Ch. Wohlfarth

2009-01-01T23:59:59.000Z

238

Dielectric constant of the mixture (1) water; (2) tetrahydrothiophene-1,1-dioxide  

Science Journals Connector (OSTI)

Substance name(s): tetrahydrothiophene-1,1-dioxide; tetrahydrothiophene-S,S-dioxide; tetrahydro-thiophene-1,1 ... ,1-dioxide; thiacyclopentane dioxide; tetramethylene sulfone; tetrahydrothiophene 1...

Ch. Wohlfarth

2008-01-01T23:59:59.000Z

239

Viscosity of the mixture (1) tetrahydrothiophene-1,1-dioxide; (2) 1,4-dimethylbenzene  

Science Journals Connector (OSTI)

Substance name(s): tetrahydrothiophene-1,1-dioxide; tetrahydrothiophene-S,S-dioxide; tetrahydro-thiophene-1,1 ... ,1-dioxide; thiacyclopentane dioxide; tetramethylene sulfone; tetrahydrothiophene 1...

Ch. Wohlfarth

2009-01-01T23:59:59.000Z

240

Viscosity of the mixture (1) tetrahydrothiophene-1,1-dioxide; (2) toluene  

Science Journals Connector (OSTI)

Substance name(s): tetrahydrothiophene-1,1-dioxide; tetrahydrothiophene-S,S-dioxide; tetrahydro-thiophene-1,1 ... ,1-dioxide; thiacyclopentane dioxide; tetramethylene sulfone; tetrahydrothiophene 1...

Ch. Wohlfarth

2009-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "reduce sulfur dioxide" 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

Refractive index of the mixture (1) tetrahydrothiophene-1,1-dioxide; (2) 1-methylnapthalene  

Science Journals Connector (OSTI)

Substance name(s): tetrahydrothiophene-1,1-dioxide; tetrahydrothiophene-S,S-dioxide; tetrahydro-thiophene-1,1 ... ,1-dioxide; thiacyclopentane dioxide; tetramethylene sulfone; tetrahydrothiophene 1...

Ch. Wohlfarth

2008-01-01T23:59:59.000Z

242

Viscosity of the mixture (1) 1,3-dioxolane; (2) tetrahydrothiophene-1,1-dioxide  

Science Journals Connector (OSTI)

Substance name(s): tetrahydrothiophene-1,1-dioxide; tetrahydrothiophene-S,S-dioxide; tetrahydro-thiophene-1,1 ... ,1-dioxide; thiacyclopentane dioxide; tetramethylene sulfone; tetrahydrothiophene 1...

Ch. Wohlfarth

2009-01-01T23:59:59.000Z

243

Viscosity of the mixture (1) water; (2) tetrahydrothiophene-1,1-dioxide  

Science Journals Connector (OSTI)

Substance name(s): tetrahydrothiophene-1,1-dioxide; tetrahydrothiophene-S,S-dioxide; tetrahydro-thiophene-1,1 ... ,1-dioxide; thiacyclopentane dioxide; tetramethylene sulfone; tetrahydrothiophene 1...

Ch. Wohlfarth

2009-01-01T23:59:59.000Z

244

Viscosity of the mixture (1) tetrahydrothiophene-1,1-dioxide; (2) 1,3-dimethylbenzene  

Science Journals Connector (OSTI)

Substance name(s): tetrahydrothiophene-1,1-dioxide; tetrahydrothiophene-S,S-dioxide; tetrahydro-thiophene-1,1 ... ,1-dioxide; thiacyclopentane dioxide; tetramethylene sulfone; tetrahydrothiophene 1...

Ch. Wohlfarth

2009-01-01T23:59:59.000Z

245

Viscosity of the mixture (1) tetrahydrothiophene-1,1-dioxide; (2) benzene  

Science Journals Connector (OSTI)

Substance name(s): tetrahydrothiophene-1,1-dioxide; tetrahydrothiophene-S,S-dioxide; tetrahydro-thiophene-1,1 ... ,1-dioxide; thiacyclopentane dioxide; tetramethylene sulfone; tetrahydrothiophene 1...

Ch. Wohlfarth

2009-01-01T23:59:59.000Z

246

Viscosity of the mixture (1) tetrahydrofuran; (2) tetrahydrothiophene-1,1-dioxide  

Science Journals Connector (OSTI)

Substance name(s): tetrahydrothiophene-1,1-dioxide; tetrahydrothiophene-S,S-dioxide; tetrahydro-thiophene-1,1 ... ,1-dioxide; thiacyclopentane dioxide; tetramethylene sulfone; tetrahydrothiophene 1...

Ch. Wohlfarth

2009-01-01T23:59:59.000Z

247

Viscosity of the mixture (1) tetrahydrothiophene-1,1-dioxide; (2) 1,2-dimethylbenzene  

Science Journals Connector (OSTI)

Substance name(s): tetrahydrothiophene-1,1-dioxide; tetrahydrothiophene-S,S-dioxide; tetrahydro-thiophene-1,1 ... ,1-dioxide; thiacyclopentane dioxide; tetramethylene sulfone; tetrahydrothiophene 1...

Ch. Wohlfarth

2009-01-01T23:59:59.000Z

248

Fact #824: June 9, 2014 EPA Sulfur Standards for Gasoline  

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

Sulfur naturally occurs in gasoline and diesel fuel, contributing to pollution when the fuel is burned. Beginning in 2004, standards were set on the amount of sulfur in gasoline (Tier 2 standards)....

249

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

250

ORIGINAL ARTICLE Sulfur oxidizers dominate carbon fixation  

E-Print Network (OSTI)

). Methylotrophs and iron oxidizers were also active in plume waters and expressed key proteins for methane by bacteria (especially, alpha-, gamma- and epsilon-proteobacteria) that likely participate in the oxidationORIGINAL ARTICLE Sulfur oxidizers dominate carbon fixation at a biogeochemical hot spot in the dark

Hansell, Dennis

251

High-Sulfur Coal for Generating Electricity  

Science Journals Connector (OSTI)

...amounts of coal, because...Director-Mineral Re-sources...of Gas from Coal through a...on coals of high ash-fusion temperature...per ton of high-sulfur coal burned. Absorp-tion...particulate matter as well as...capable of remov-ing up to...

James T. Dunham; Carl Rampacek; T. A. Henrie

1974-04-19T23:59:59.000Z

252

Short communication Influence of molybdenum and sulfur on copper  

E-Print Network (OSTI)

Short communication Influence of molybdenum and sulfur on copper metabolism in sheep: comparison of molybdenum able to trigger the copper sulfur molybdenum interference in sheep was measured with either only) and 4 increasing molybdenum doses. The sulfur-molybdenum-copper interference was quantified

Paris-Sud XI, Université de

253

A novel lithium/sulfur battery based on sulfur/graphene nanosheet composite cathode and gel polymer electrolyte  

Science Journals Connector (OSTI)

A novel sulfur/graphene nanosheet (S/GNS) composite was prepared ... ball milling of sulfur with commercial multi-layer graphene nanosheet, followed by a heat treatment. ... of irregularly interlaced nanosheet-li...

Yongguang Zhang; Yan Zhao; Zhumabay Bakenov

2014-03-01T23:59:59.000Z

254

A simple approach to synthesize nanosized sulfur/graphene oxide materials for high-performance lithium/sulfur batteries  

Science Journals Connector (OSTI)

We report on a simple and facile synthesis route for the sulfur/graphene oxide composite via ultrasonic mixing of the nano-sulfur and graphene oxide aqueous suspensions followed by a low-temperature heat treat...

Yongguang Zhang; Yan Zhao; Zhumabay Bakenov

2014-07-01T23:59:59.000Z

255

An analysis of the impact of having uranium dioxide mixed in with plutonium dioxide  

SciTech Connect

An assessment was performed to show the impact on airborne release fraction, respirable fraction, dose conversion factor and dose consequences of postulated accidents at the Plutonium Finishing Plant involving uranium dioxide rather than plutonium dioxide.

MARUSICH, R.M.

1998-10-21T23:59:59.000Z

256

Sulfur accumulation in pinewood (Pinus sylvestris) induced by bacteria in a simulated seabed environment: Implications for marine archaeological wood and fossil fuels  

Science Journals Connector (OSTI)

Fresh pinewood blocks were submerged in sulfate and iron(II) containing media, inoculated with bacterial consortia isolated from seawater, aiming to simulate the seabed conditions of the Vasa shipwreck (1628). The consortia contained erosion (EB) and sulfate-reducing bacteria (SRB). Sulfur K-edge X-ray absorption near edge structure (XANES) spectroscopy and scanning X-ray spectromicroscopy images showed that organic sulfur, mainly thiols (R-SH), had accumulated in the lignin-rich middle lamella in EB-degraded parts of the wood. The sulfur content in the wood increased more than 10 times in 2 years. In another series with active inoculums from marine archaeological wood, the sulfur XANES spectra showed, after 4 years of anaerobic treatment, considerable amounts also of inorganic iron sulfides, Fe1?xS, which oxidized at atmospheric exposure. A sediment sample from the Vasa's seabed was also rich in iron sulfides, including pyrite, FeS2. X-ray fluorescence mappings of sulfur and phosphorous distributions indicate that scavenging SRB penetration, producing hydrogen sulfide in situ, is restricted to EB-degraded parts of the wood structure. The sulfur isotope depletion of 34S from ?34S = 21‰ in marine sulfate to ?34S = 6‰ and 1.8‰ for fractions of reduced sulfur and sulfate separated from a Vasa wood sample, respectively, suggests bacterial transformation. A fuller understanding of the routes of sulfur accumulation, as reactive iron sulfides and as organic sulfur, has important implications for improving conservation methods of marine archaeological wood. Moreover, the biogenic accumulation of organically bound sulfur, specifically in lignin-rich parts of waterlogged wood, has wider geochemical significance for fossil fuels of marine origin, as lignin-rich humic matter is important for the diagenetic formation of kerogens from anoxic marine sediments.

Yvonne Fors; Thomas Nilsson; Emiliana Damian Risberg; Magnus Sandström; Peter Torssander

2008-01-01T23:59:59.000Z

257

ULTRA-LOW SULFUR REDUCTION EMISSION CONTROL DEVICE/DEVELOPMENT OF AN ON-BOARD FUEL SULFUR TRAP  

SciTech Connect

Honeywell is actively working on a 3-year program to develop and demonstrate proof-of-concept for an ''on-vehicle'' desulfurization fuel filter for heavy-duty diesel engines. Integration of the filter into the vehicle fuel system will reduce the adverse effects sulfur has on post combustion emission control devices such as NO{sub x} adsorbers. The NO{sub x} adsorber may be required to meet the proposed new EPA Tier II and ''2007-Rule'' emission standards. The proposed filter concept is based on Honeywell's reactive filtration technology and experience in liquids handling and conditioning. A regeneration and recycling plan for the spent filters will also be examined. We have chosen to develop and demonstrate this technology based on criteria set forth for a heavy duty CIDI engine system because it represents a more challenging set of conditions of service intervals and overall fuel usage over light duty systems. It is anticipated that the technology developed for heavy-duty applications will be applicable to light-duty as well. Further, technology developed under this proposal would also have application for the use of liquid based fuels for fuel cell power generation. The program consists of four phases. Phase I will focus on developing a concept design and analysis and resolution of technical barriers concerning removal of sulfur-containing species in low sulfur fuels. In Phase II we will concentrate on prototype filter design and preparation followed by qualification testing of this component in a fuel line application. Phase III will study life cycle and regeneration options for the spent filter. Phase IV will focus on efficacy and life testing and component integration. The project team will include a number of partners, with Honeywell International as the prime contractor. The partners include an emission control technology developer (Honeywell International), a fuel technology developer (Marathon Ashland Petroleum), a catalyst technology developer (Johnson Matthey), a CIDI engine manufacturer (Mack Trucks Inc.), a filter recycler (American Wastes Industries), and a low-sulfur fuel supplier (Equilon, a joint venture between Shell and Texaco).

Ron Rohrbach; Gary Zulauf; Tim Gavin

2003-04-01T23:59:59.000Z

258

Putting the pressure on carbon dioxide | EMSL  

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

Putting the pressure on carbon dioxide Improving the chances for fuel recovery and carbon sequestration Artwork from this research graces the cover of Environmental Science...

259

Club Convergence in Carbon Dioxide Emissions  

Science Journals Connector (OSTI)

We examine convergence in carbon dioxide emissions among 128 countries for the period 1960–...2 emissions among all the countries under scrutiny in...

Ekaterini Panopoulou; Theologos Pantelidis

2009-09-01T23:59:59.000Z

260

The use of ethanol to remove sulfur from coal. Final report, September 1991--December 1992  

SciTech Connect

In developing the new Ohio University procedure the thermodynamic limitations of the reactions for removal of both pyritic and organic sulfur from coal at 400--600{degrees}C were studied using copper as a very strong H{sub 2}S-acceptor. Copper serves as a catalyst for ethanol dehydrogenation to form nascent hydrogen. Copper also serves as a scavenger to form copper sulfide from the hydrogen sulfide evolved during the reaction. Copper sulfide in turn serves as a catalyst for organic sulfur hydrodesulfurization reactions. If the coal to be desulfurized contains pyrite (FeS{sub 2}) or FeS, the copper scavenger effect reduces any back reaction of hydrogen sulfide with the iron and increases the removal of sulfur from the carbonaceous material. The desired effect of using copper can be achieved by using copper or copper containing alloys as materials of construction or as liners for a regenerable reactor. During the time period that Ohio Coal Development Office supported this work, small scale (560 grams) laboratory experiments with coals containing about 3.5% sulfur have achieved up to 90% desulfurization at temperatures of 500{degrees}C when using a copper reactor. Results from the autoclave experiments have identified the nature of the chemical reactions taking place. Because the process removes both pyritic and organic sulfur in coal, the successful scale up of the process would have important economic significance to the coal industry. Even though this and other chemical processes may be relatively expensive and far from being commercial, the reason for further development is that this process may hold the promise of achieving much greater sulfur reduction and of producing a cleaner coal than other methods. This would be especially important for small or older power plants and industrial boilers.

Not Available

1993-04-15T23:59:59.000Z

Note: This page contains sample records for the topic "reduce sulfur dioxide" 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

Graphene-Wrapped Sulfur Particles as a Rechargeable Lithium–Sulfur Battery Cathode Material with High Capacity and Cycling Stability  

Science Journals Connector (OSTI)

Graphene-Wrapped Sulfur Particles as a Rechargeable Lithium–Sulfur Battery Cathode Material with High Capacity and Cycling Stability ... The resulting graphene–sulfur composite showed high and stable specific capacities up to ?600 mAh/g over more than 100 cycles, representing a promising cathode material for rechargeable lithium batteries with high energy density. ...

Hailiang Wang; Yuan Yang; Yongye Liang; Joshua Tucker Robinson; Yanguang Li; Ariel Jackson; Yi Cui; Hongjie Dai

2011-06-24T23:59:59.000Z

262

NiW and NiRu Bimetallic Catalysts for Ethylene Steam Reforming: Alternative Mechanisms for Sulfur Resistance  

SciTech Connect

Previous investigations of Ni-based catalysts for the steam reforming of hydrocarbons have indicated that the addition of a second metal can reduce the effects of sulfur poisoning. Two systems that have previously shown promise for such applications, NiW and NiRu, are considered here for the steam reforming of ethylene, a key component of biomass derived tars. Monometallic and bimetallic Al{sub 2}O{sub 3}-supported Ni and W catalysts were employed for ethylene steam reforming in the presence and absence of sulfur. The NiW catalysts were less active than Ni in the absence of sulfur, but were more active in the presence of 50 ppm H{sub 2}S. The mechanism for the W-induced improvements in sulfur resistance appears to be different from that for Ru in NiRu. To probe reasons for the sulfur resistance of NiRu, the adsorption of S and C{sub 2}H{sub 4} on several bimetallic NiRu alloy surfaces ranging from 11 to 33 % Ru was studied using density functional theory (DFT). The DFT studies reveal that sulfur adsorption is generally favored on hollow sites containing Ru. Ethylene preferentially adsorbs atop the Ru atom in all the NiRu (111) alloys investigated. By comparing trends across the various bimetallic models considered, sulfur adsorption was observed to be correlated with the density of occupied states near the Fermi level while C{sub 2}H{sub 4} adsorption was correlated with the number of unoccupied states in the d-band. The diverging mechanisms for S and C{sub 2}H{sub 4} adsorption allow for bimetallic surfaces such as NiRu that enhance ethylene binding without accompanying increases in sulfur binding energy. In contrast, bimetallics such as NiSn and NiW appear to decrease the affinity of the surface for both the reagent and the poison.

Rangan, M.; Yung, M. M.; Medlin, J. W.

2012-06-01T23:59:59.000Z

263

Carbon-dioxide-controlled ventilation study  

SciTech Connect

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

264

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 are valued using the "real options" valuation methodology in an uncertain carbon dioxide (CO2) price (baseline IGCC), and IGCC with pre-investments that make future retrofit for CO2 capture less expensive (pre

265

Optimize carbon dioxide sequestration, enhance oil recovery  

E-Print Network (OSTI)

- 1 - Optimize carbon dioxide sequestration, enhance oil recovery January 8, 2014 Los Alamos simulation to optimize carbon dioxide (CO2) sequestration and enhance oil recovery (CO2-EOR) based on known production. Due to carbon capture and storage technology advances, prolonged high oil prices

266

Predicting Future Atmospheric Carbon Dioxide Levels  

Science Journals Connector (OSTI)

...Predicting future atmospheric carbon dioxide levels...1978012175 air atmosphere biosphere carbon...Predicting future atmospheric carbon dioxide levels...re-quired 5-Mhz bandwidth, which...synchronization rate of 16 khz and the picture...the interstellar plasma. For UHF frequencies...

U. Siegenthaler; H. Oeschger

1978-01-27T23:59:59.000Z

267

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...

268

Table 2. 2011 State energy-related carbon dioxide emisssions...  

Annual Energy Outlook 2012 (EIA)

2011 State energy-related carbon dioxide emissions by fuel million metric tons of carbon dioxide shares State Coal Petroleum Natural Gas Total Coal Petroleum Natural Gas Alabama...

269

Reducing NOx in Fired Heaters and Boilers  

E-Print Network (OSTI)

-6, 2000 Reducing NOx in Fired Heaters Air Pollution Control and Boilers Keeping the environment clean Presented by Ashutosh Garg Furnace Improvements Low cost solutions for fired heaters Trace compounds ? Nitric oxides ? Carbon monoxide ? Sulfur... it is essential to estimate accurately baseline NOx emissions. ? This will establish each units current compliance status. ? Emissions ? Current excess air level ? Carbon monoxide ? Combustibles ? NOx corrected to 3% 02 314 ESL-IE-00-04-46 Proceedings...

Garg, A.

270

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

271

Sulfur-isotope separation by distillation  

SciTech Connect

Sulfur-isotope separation by low-temperature distillation of hydrogen sulfide was studied in an 8-m, 25-mm diameter distillation column. Column temperature was controlled by a propane-propylene heat pipe. Column packing HETP was measured using nitric oxide in the column. The column was operated at pressures from 45 to 125 kPa. The relative volatility of S-32 vs. S-34 varied from 1.0008 to 1.0014.

Mills, T.R.

1982-01-01T23:59:59.000Z

272

Sulfur/three-dimensional graphene composite for high performance lithium–sulfur batteries  

Science Journals Connector (OSTI)

Abstract A sulfur/graphene composite is prepared by loading elemental sulfur into three-dimensional graphene (3D graphene), which is assembled using a metal ions assisted hydrothermal method. When used as cathode materials for lithium–sulfur (Li–S) batteries, the sulfur/graphene composite (S@3D-graphene) with 73 wt % sulfur shows a significantly enhanced cycling performance (>700 mAh g?1 after 100 cycles at 0.1C rate with a Coulombic efficiency > 96%) as well as high rate capability with a capacity up to 500 mAh g?1 at 2C rate (3.35 A g?1). The superior electrochemical performance could be attributed to the highly porous structure of three-dimensional graphene that not only enables stable and continue pathway for rapid electron and ion transportation, but also restrain soluble polysulfides and suppress the “shuttle effect”. Moreover, the robust structure of 3D graphene can keep cathode integrity and accommodate the volume change during high-rate charge/discharge processes, making it a promising candidate as cathode for high performance Li–S batteries.

Chunmei Xu; Yishan Wu; Xuyang Zhao; Xiuli Wang; Gaohui Du; Jun Zhang; Jiangping Tu

2015-01-01T23:59:59.000Z

273

Carbon dioxide emission, institutional quality, and economic growth: Empirical evidence in Malaysia  

Science Journals Connector (OSTI)

Abstract In view of Malaysia's status as a fast-growing economy with accelerating carbon dioxide emissions, a better understanding of the relationship between economic growth and pollution is vital to the policy makers. This paper, therefore, attempts to investigate the existence of long run relationship among carbon dioxide emission, institutional quality, exports, and economic growth and further examines the causal relationship among these variables in Malaysia for the period 1984–2008. From the bounds test, it is found that a long run relationship does exist among the variables, even using different conditioning information sets. A positive and significant interaction term between carbon dioxide emission and institutional quality indicator (i.e. law and order) implies that good institutional quality is important in controlling carbon dioxide emission in the process of economic development. The results for Granger causality tests further confirm the importance of institutional frameworks in reducing carbon dioxide emissions since institutional quality is found not only affects economic growth directly, but also indirectly via carbon dioxide emissions. This indicates that sound institutional frameworks are essential for Malaysia to achieve high economic growth without sacrificing its environment.

Lin-Sea Lau; Chee-Keong Choong; Yoke-Kee Eng

2014-01-01T23:59:59.000Z

274

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

275

Supercritical Carbon Dioxide Turbo-Expander and Heat Exchangers  

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

This fact sheet describes a supercritical carbon dioxide turbo-expander and heat exchangers project awarded under the DOE's 2012 SunShot Concentrating Solar Power R&D award program. The team, led by the Southwest Research Institute, is working to develop a megawatt-scale s-CO2 hot-gas turbo-expander optimized for the highly transient solar power plant profile. The team is also working to optimize novel printed circuit heat exchangers for s-CO2 applications to drastically reduce their manufacturing costs.

276

Project Profile: Direct Supercritical Carbon Dioxide Receiver Development  

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

The National Renewable Energy Laboratory (NREL), under the National Laboratory R&D competitive funding opportunity, is working to develop, characterize, and experimentally demonstrate a novel high-temperature receiver technology using supercritical carbon dioxide (s-CO2) directly as the heat transfer fluid (HTF). A high-temperature receiver that is compatible with s-CO2 enables a significant increase in power cycle efficiency and reduces solar-field size, thereby decreasing the installed cost of concentrating solar power (CSP) systems.

277

American Electric Power (AEP): Mountaineer Carbon Dioxide Capture and Storage Demonstration (WITHDRAWN AT CONCLUSION OF PHASE 1)  

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

American Electric Power (AEP): American Electric Power (AEP): Mountaineer Carbon Dioxide Capture and Storage Demonstration (WITHDRAWN AT CONCLUSION OF PHASE 1) Background A need exists to further develop carbon management technologies that capture and store or beneficially reuse carbon dioxide (CO 2 ) that would otherwise be emitted into the atmosphere from coal-based electric power generating facilities. Carbon capture, utilization and storage (CCUS) technologies offer great potential for reducing CO

278

Reduce Stress!  

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

Stress! Stress! x Take a break every hour. Do some relaxation or stretching exercises or talk with someone about topics unrelated to work. Give your body and mind a rest. x Massage your hands and forearms several times a day with a vitamin E lotion. The massage will improve circulation and break up adhesions. Since you can't touch a keyboard until the lotion is absorbed, it also enforces a good break. x Massage the muscles in your neck working your way down from the skull to the shoulders, applying more force to the larger muscles as you go down. x Periodically evaluate your environment for ways to reduce stress. Try to keep your desk uncluttered so you can always find things. Make sure programs are set up correctly on the computer, and see if you can use a macro program to reduce

279

Enzymatic conversion of carbon dioxide to methanol: Enhanced methanol production in silica sol-gel matrices  

SciTech Connect

Strategies for effective conversion of atmospheric CO{sub 2} to methanol offer promising new technologies not only for recycling of the greenhouse gas but also for an efficient production of fuel alternatives. Partial hydrogenation of carbon dioxide has been accomplished by means of heterogeneous catalysis, electrocatalysis, and photocatalysis. Oxide-based catalysts are predominantly used for industrial fixation of carbon dioxide. A unique approach in this direction involves the use of enzymes as catalysts for conversion of carbon dioxide to methanol. The use of enzymes is particularly appealing since it provides a facile low-temperature route for generation of methanol directly from gaseous carbon dioxide. The authors report an enzymatically coupled sequential reduction of carbon dioxide to methanol by using a series of reactions catalyzed by three different dehydrogenases. Overall, the process involves an initial reduction of CO{sub 2} to formate catalyzed by formate dehydrogenase (F{sub ate}DH), followed by reduction of formate to formaldehyde by formaldehyde dehydrogenase (F{sub ald}DH), and finally formaldehyde is reduced to methanol by alcohol dehydrogenase (ADH). In this process, reduced nicotinamide adenine dinucleotide (NADH) acts as a terminal electron donor for each dehydrogenase-catalyzed reduction.

Obert, R.; Dave, B.C.

1999-12-29T23:59:59.000Z

280

Conversion of Hydrogen Sulfide in Coal Gases to Liquid Elemental Sulfur with Monolithic Catalysts  

SciTech Connect

Removal of hydrogen sulfide (H{sub 2}S) from coal gasifier gas and sulfur recovery are key steps in the development of Department of Energy's (DOE's) advanced power plants that produce electric power and clean transportation fuels with coal and natural gas. These plants will require highly clean coal gas with H{sub 2}S below 1 ppmv and negligible amounts of trace contaminants such as hydrogen chloride, ammonia, alkali, heavy metals, and particulate. The conventional method of sulfur removal and recovery employing amine, Claus, and tail-gas treatment is very expensive. A second generation approach developed under DOE's sponsorship employs hot-gas desulfurization (HGD) using regenerable metal oxide sorbents followed by Direct Sulfur Recovery Process (DSRP). However, this process sequence does not remove trace contaminants and is targeted primarily towards the development of advanced integrated gasification combined cycle (IGCC) plants that produce electricity (not both electricity and transportation fuels). There is an immediate as well as long-term need for the development of cleanup processes that produce highly clean coal gas for next generation power plants. To this end, a novel process is now under development at several research organizations in which the H{sub 2} in coal gas is directly oxidized to elemental sulfur over a selective catalyst. Such a process is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S In the Single-Step Sulfur Recovery Process (SSRP), the direct oxidation of H{sub 2}S to elemental sulfur in the presence of SO{sub 2} is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S. This direct oxidation process has the potential to produce a super clean coal gas more economically than both conventional amine-based processes and HGD/DSRP. The H{sub 2} and CO components of syngas appear to behave as inert with respect to sulfur formed at the SSRP conditions. One problem in the SSRP process that needs to be eliminated or minimized is COS formation that may occur due to reaction of CO with sulfur formed from the Claus reaction. The objectives of this research are to formulate monolithic catalysts for removal of H{sub 2}S from coal gases and minimum formation of COS with monolithic catalyst supports, {gamma}-alumina wash or carbon coats, and catalytic metals, to develop a catalytic regeneration method for a deactivated monolithic catalyst, to measure kinetics of both direct oxidation of H{sub 2}S to elemental sulfur with SO{sub 2} as an oxidizer and formation of COS in the presence of a simulated coal gas mixture containing H{sub 2}, CO, CO{sub 2}, and moisture, using a monolithic catalyst reactor, and to develop kinetic rate equations and model the direct oxidation process to assist in the design of large-scale plants. This heterogeneous catalytic reaction has gaseous reactants such as H{sub 2}S and SO{sub 2}. However, this heterogeneous catalytic reaction has heterogeneous products such as liquid elemental sulfur and steam. To achieve the above-mentioned objectives using a monolithic catalyst reactor, experiments on conversion of hydrogen sulfide into elemental sulfur and formation of COS were carried out for the space time range of 40-560 seconds at 120-150 C to evaluate effects of reaction temperatures, total pressure, space time, and catalyst regeneration on conversion of hydrogen sulfide into elemental sulfur and formation of COS. Simulated coal gas mixtures consist of 3,600-4,000-ppmv hydrogen sulfide, 1,800-2,000 ppmv sulfur dioxide, 23-27 v% hydrogen, 36-41 v% CO, 10-12 v% CO{sub 2}, 0-10 vol % moisture, and nitrogen as remainder. Volumetric feed rates of a simulated coal gas mixture to the reactor are 30-180 SCCM. The temperature of the reactor is controlled in an oven at 120-150 C. The pressure of the reactor is maintained at 40-210 psia. The molar ratio of H{sub 2}S to SO{sub 2} in the monolithic catalyst reactor is mai

K. C. Kwon

2006-09-30T23:59:59.000Z

Note: This page contains sample records for the topic "reduce sulfur dioxide" 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

FETC Programs for Reducing Greenhouse Gas Emissions  

SciTech Connect

Mark Twain once quipped that everyone talks about the weather but no one does anything about it. With interest in global climate change on the rise, researchers in the fossil-energy sector are feeling the heat to provide new technology to permit continued use of fossil fuels but with reduced emissions of so-called `greenhouse gases.` Three important greenhouse gases, carbon dioxide, methane, and nitrous oxide, are released to the atmosphere in the course of recovering and combusting fossil fuels. Their importance for trapping radiation, called forcing, is in the order given. In this report, we briefly review how greenhouse gases cause forcing and why this has a warming effect on the Earth`s atmosphere. Then we discuss programs underway at FETC that are aimed at reducing emissions of methane and carbon dioxide.

Ruether, J.A.

1998-02-01T23:59:59.000Z

282

Lithium/Sulfur Batteries Based on Doped Mesoporous Carbon - Energy...  

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

Materials Advanced Materials Find More Like This Return to Search LithiumSulfur Batteries Based on Doped Mesoporous Carbon Oak Ridge National Laboratory Contact ORNL About...

283

Analyses of sulfur-asphalt field trials in Texas  

E-Print Network (OSTI)

128 LIST OF FIGURES FIGURE PAGF Layout of SNPA sulfur bitumen binder pavem nt test ? U. S. Highway 69, Lufkin, Texas 15 Col 1oi d mi 1 1 furnished by SNPA for preparation of sul fur-asphalt emulsions View of mixing station showing sulfur... designed to investigate the advantage of using a colloid mill to prepare sulfur-asphalt binders as compared to comingling the asphalt and molten sulfur in a pipeline leading directly to the pug mill. After only six months of testing, the results...

Newcomb, David Edward

1979-01-01T23:59:59.000Z

284

Development of sulfur cathode material for Li-S batteries.  

E-Print Network (OSTI)

??M.S. Efforts were taken to fabricate a cathode material having Sulfur as the active material. First step is composed of identifying potential ways of fabricating… (more)

Dharmasena, Ruchira Ravinath, 1984-

2014-01-01T23:59:59.000Z

285

Project Profile: Baseload CSP Generation Integrated with Sulfur...  

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

Related Links FAQs Contact Us Offices You are here Home Concentrating Solar Power Project Profile: Baseload CSP Generation Integrated with Sulfur-Based...

286

SULFUR-TOLERANT CATALYST FOR THE SOLID OXIDE FUEL CELL.  

E-Print Network (OSTI)

??JP-8 fuel is easily accessible, transportable, and has hydrogen content essential to solid oxide fuel cell (SOFC) operation. However, this syngas has sulfur content which… (more)

Bozeman, Joe Frank, III

2010-01-01T23:59:59.000Z

287

Fundamental Studies of Lithium-Sulfur Cell Chemistry  

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

Studies of Lithium-Sulfur Cell Chemistry PI: Nitash Balsara LBNL June 17, 2014 Project ID ESS224 This presentation does not contain any proprietary, confidential, or otherwise...

288

Abatement of Air Pollution: Control of Sulfur Compound Emissions  

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

Abatement of Air Pollution: Control of Sulfur Compound Emissions Abatement of Air Pollution: Control of Sulfur Compound Emissions (Connecticut) Abatement of Air Pollution: Control of Sulfur Compound Emissions (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 Program Info State Connecticut Program Type Environmental Regulations Provider Department of Energy and Environmental Protection These regulations set limits on the sulfur content of allowable fuels (1.0%

289

Improvement of LNG production technology in gas-distribution stations with an increased content of carbon dioxide in supply-line gas  

Science Journals Connector (OSTI)

The possibility is considered of reducing the weight of absorbent in a carbon dioxide gas cleaning system during liquefied natural gas production in gas-distribution stations (due to use of a pressure drop ... is...

S. P. Gorbachev; S. V. Lyugai

2009-11-01T23:59:59.000Z

290

Effects of Nitrogen and Sulfur Fertilization on Free Amino Acids, Sugars, and Acrylamide-Forming Potential in Potato  

Science Journals Connector (OSTI)

In this study, 13 varieties of potato were grown in a field trial in 2010 and treated with different combinations of N and S. Potatoes were analyzed immediately after harvest to show the effect of N and S fertilization on concentrations of free asparagine, other free amino acids, sugars, and acrylamide-forming potential. ... (4-7) With respect to potato, De Wilde et al. showed that concentrations of sugars in tubers rose in response to N deprivation by up to 100% compared with adequately fertilized potatoes,(8) and Kumar et al. similarly reported that plants adequately fertilized with N had lower reducing sugar concentration at harvest. ... To examine how sulfur deprivation may affect acrylamide formation in cooked potatoes, three varieties of potato were grown under conditions of either severe sulfur deprivation or an adequate supply of sulfur. ...

Nira Muttucumaru; Stephen J. Powers; J. Stephen Elmore; Donald S. Mottram; Nigel G. Halford

2013-06-15T23:59:59.000Z

291

Sulfur removal and comminution of carbonaceous material  

DOE Patents (OSTI)

Finely divided, clean coal or other carbonaceous material is provided by forming a slurry of coarse coal in aqueous alkali solution and heating the slurry under pressure to above the critical conditions of steam. The supercritical fluid penetrates and is trapped in the porosity of the coal as it swells in a thermoplastic condition at elevated temperature. By a sudden, explosive release of pressure the coal is fractured into finely divided particles with release of sulfur-containing gases and minerals. The finely divided coal is recovered from the minerals for use as a clean coal product. 2 figs.

Narain, N.K.; Ruether, J.A.; Smith, D.N.

1987-10-07T23:59:59.000Z

292

Sulfur removal and comminution of carbonaceous material  

DOE Patents (OSTI)

Finely divided, clean coal or other carbonaceous material is provided by forming a slurry of coarse coal in aqueous alkali solution and heating the slurry under pressure to above the critical conditions of steam. The supercritical fluid penetrates and is trapped in the porosity of the coal as it swells in a thermoplastic condition at elevated temperature. By a sudden, explosive release of pressure the coal is fractured into finely divided particles with release of sulfur-containing gases and minerals. The finely divided coal is recovered from the minerals for use as a clean coal product.

Narain, Nand K. (Bethel Park, PA); Ruether, John A. (McMurray, PA); Smith, Dennis N. (Herminie, PA)

1988-01-01T23:59:59.000Z

293

Sulfur isotopes in coal constrain the evolution of the Phanerozoic sulfur cycle  

Science Journals Connector (OSTI)

...obviously influence the average isotope values. For the other data, samples...pp 87–105 . 19 Price FT Casagrande DJ ( 1991 ) Sulfur...coals. Geology of Fossil Fuels, Proc 30th Int Geol Congress...Jersey Pinelands and its effect on stream water chemistry...223 – 248 . 29 Price FT Shieh YN ( 1979 ) Fractionation...

Donald E. Canfield

2013-01-01T23:59:59.000Z

294

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

295

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.

1994-01-01T23:59:59.000Z

296

Storage of Carbon Dioxide in Offshore Sediments  

Science Journals Connector (OSTI)

...Carbon Dioxide in Offshore Sediments 10...efforts to increase energy efficiency; efforts...sources, including renewable and nuclear energy; and investment...repositories. Offshore geological repositories...between Scotland and Norway and far out of...

Daniel P. Schrag

2009-09-25T23:59:59.000Z

297

Production of elemental sulfur and ammonium thiosulfate by the oxidation of H2S containing water vapor and ammonia over V/Zr-PILC catalysts  

Science Journals Connector (OSTI)

The catalytic oxidation of hydrogen sulfide in the presence of water and ammonia was studied over V2O5 supported on Zr-pillared clay catalysts (V/Zr-PILCs). The synthesized catalysts were examined using a variety of characterization techniques. A catalytic performance study using V/Zr-PILC catalysts showed that H2S was successfully converted to elemental sulfur and ammonium thiosulfate (ATS) without considerable emission of sulfur dioxide. The H2S conversion over V/Zr-PILCs increased with increasing the content of vanadia up to 6 wt.%. This superior catalytic performance might be related to the uniform dispersion of vanadia species on the Zr-PILC support.

Kanattukara Vijayan Bineesh; Moon-il Kim; Goo-Hwa Lee; Manickam Selvaraj; Kyu Hyun; Dae-Won Park

2012-01-01T23:59:59.000Z

298

Conversion of Hydrogen Sulfide in Coal Gases to Liquid Elemental Sulfur with Monolithic Catalysts  

SciTech Connect

Removal of hydrogen sulfide (H{sub 2}S) from coal gasifier gas and sulfur recovery are key steps in the development of Department of Energy's (DOE's) advanced power plants that produce electric power and clean transportation fuels with coal and natural gas. These plants will require highly clean coal gas with H{sub 2}S below 1 ppmv and negligible amounts of trace contaminants such as hydrogen chloride, ammonia, alkali, heavy metals, and particulate. The conventional method of sulfur removal and recovery employing amine, Claus, and tail-gas treatment is very expensive. A second generation approach developed under DOE's sponsorship employs hot-gas desulfurization (HGD) using regenerable metal oxide sorbents followed by Direct Sulfur Recovery Process (DSRP). However, this process sequence does not remove trace contaminants and is targeted primarily towards the development of advanced integrated gasification combined cycle (IGCC) plants that produce electricity (not both electricity and transportation fuels). There is an immediate as well as long-term need for the development of cleanup processes that produce highly clean coal gas for next generation power plants. To this end, a novel process is now under development at several research organizations in which the H{sub 2}S in coal gas is directly oxidized to elemental sulfur over a selective catalyst. Such a process is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S In the Single-Step Sulfur Recovery Process (SSRP), the direct oxidation of H{sub 2}S to elemental sulfur in the presence of SO{sub 2} is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S. This direct oxidation process has the potential to produce a super clean coal gas more economically than both conventional amine-based processes and HGD/DSRP. The H{sub 2} and CO components of syngas appear to behave as inert with respect to sulfur formed at the SSRP conditions. One problem in the SSRP process that needs to be eliminated or minimized is COS formation that may occur due to reaction of CO with sulfur formed from the Claus reaction. The objectives of this research are to formulate monolithic catalysts for removal of H{sub 2}S from coal gases and minimum formation of COS with monolithic catalyst supports, {gamma}-alumina wash or carbon coats, and catalytic metals, to develop a catalytic regeneration method for a deactivated monolithic catalyst, to measure kinetics of both direct oxidation of H{sub 2}S to elemental sulfur with SO{sub 2} as an oxidizer and formation of COS in the presence of a simulated coal gas mixture containing H{sub 2}, CO, CO{sub 2}, and moisture, using a monolithic catalyst reactor, and to develop kinetic rate equations and model the direct oxidation process to assist in the design of large-scale plants. This heterogeneous catalytic reaction has gaseous reactants such as H{sub 2}S and SO{sub 2}. However, this heterogeneous catalytic reaction has heterogeneous products such as liquid elemental sulfur and steam. Experiments on conversion of hydrogen sulfide into elemental sulfur and formation of COS were carried out for the space time range of 130-156 seconds at 120-140 C to formulate catalysts suitable for the removal of H{sub 2}S and COS from coal gases, evaluate removal capabilities of hydrogen sulfide and COS from coal gases with formulated catalysts, and develop an economic regeneration method of deactivated catalysts. Simulated coal gas mixtures consist of 3,300-3,800-ppmv hydrogen sulfide, 1,600-1,900 ppmv sulfur dioxide, 18-21 v% hydrogen, 29-34 v% CO, 8-10 v% CO{sub 2}, 5-18 vol % moisture, and nitrogen as remainder. Volumetric feed rates of a simulated coal gas mixture to the reactor are 114-132 SCCM. The temperature of the reactor is controlled in an oven at 120-140 C. The pressure of the reactor is maintained at 116-129 psia. The molar ratio of H{sub 2}S to SO{sub 2} in the monolithic catalyst reactor is

K. C. Kwon

2007-09-30T23:59:59.000Z

299

Displacement of crude oil by carbon dioxide  

E-Print Network (OSTI)

DISPLACEMENT OF CRUDE OIL BY CARBON DIOXIDE A Thesis by OLUSEGUN OMOLE Submitted to the Graduate College of Texas ASM University in part';al fulfillment of the requirement for the degree of MASTER OF SCIENCE December 1980 Major Subject...: Petroleum Engineering DISPLACEMENT OF CRUDE OIL BY CARBON DIOXIDE A Thesis by OLUSEGUN OMOLE Approved as to style and content by: hairman of Committee / (Member (Member (Member (Hea o Depart ent December 1980 ABSTRACT Displacement of Crude Oil...

Omole, Olusegun

1980-01-01T23:59:59.000Z

300

Saving Money and Reducing the Risk of Climate Change Through Greater Energy Efficiency  

Science Journals Connector (OSTI)

Improving the efficiency of specific energy-using devices such as automobiles or appliances can save consumers and the country money while reducing emissions of carbon dioxide and other pollutants. In the case...

Howard S. Geller

1991-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "reduce sulfur dioxide" 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

Dielectric constant of the mixture (1) ethane-1,2-diol; (2) tetrahydrothiophene-1,1-dioxide  

Science Journals Connector (OSTI)

Substance name(s): tetrahydrothiophene-1,1-dioxide; tetrahydrothiophene-S,S-dioxide; tetrahydro-thiophene-1,1 ... ,1-dioxide; thiacyclopentane dioxide; tetramethylene sulfone; tetrahydrothiophene 1...

Ch. Wohlfarth

2008-01-01T23:59:59.000Z

302

Refractive index of the mixture (1) ethane-1,2-diol; (2) tetrahydrothiophene-1,1-dioxide  

Science Journals Connector (OSTI)

Substance name(s): tetrahydrothiophene-1,1-dioxide; tetrahydrothiophene-S,S-dioxide; tetrahydro-thiophene-1,1 ... ,1-dioxide; thiacyclopentane dioxide; tetramethylene sulfone; tetrahydrothiophene 1...

Ch. Wohlfarth

2008-01-01T23:59:59.000Z

303

Dielectric constant of the mixture (1) tetrahydrothiophene-1,1-dioxide; (2) 2-(2-hydroxyethoxy)-ethanol  

Science Journals Connector (OSTI)

Substance name(s): tetrahydrothiophene-1,1-dioxide; tetrahydrothiophene-S,S-dioxide; tetrahydro-thiophene-1,1 ... ,1-dioxide; thiacyclopentane dioxide; tetramethylene sulfone; tetrahydrothiophene 1...

Ch. Wohlfarth

2008-01-01T23:59:59.000Z

304

Refractive index of the mixture (1) tetrahydrothiophene-1,1-dioxide; (2) 2-(2-hydroxyethoxy)-ethanol  

Science Journals Connector (OSTI)

Substance name(s): tetrahydrothiophene-1,1-dioxide; tetrahydrothiophene-S,S-dioxide; tetrahydro-thiophene-1,1 ... ,1-dioxide; thiacyclopentane dioxide; tetramethylene sulfone; tetrahydrothiophene 1...

Ch. Wohlfarth

2008-01-01T23:59:59.000Z

305

NETL: News Release - Frio Formation Test Well Injected With Carbon Dioxide  

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

19, 2004 19, 2004 Frio Formation Test Well Injected With Carbon Dioxide Researchers Perform Small Scale, Short Term Carbon Sequestration Field Test HOUSTON, TX - In the first U.S. field test to investigate the ability of brine formations to store greenhouse gasses, researchers funded by the U.S. Department of Energy are closely monitoring 1,600 tons of carbon dioxide that were injected into a mile-deep well in Texas in October. The test is providing unique data to help investigators understand the viability of geologic sequestration as a means of reducing greenhouse gas emissions. The Frio Brine Pilot experimental site is 30 miles northeast of Houston, in the South Liberty oilfield. Researchers at the University of Texas at Austin's Bureau of Economic Geology drilled a 5,753 foot injection well earlier this year, and developed a nearby observation well to study the ability of the high-porosity Frio sandstone formation to store carbon dioxide.

306

HEALTH AND CLIMATE POLICY IMPACTS ON SULFUR EMISSION CONTROL  

E-Print Network (OSTI)

the climate and health effects of sulfate aerosol into an integrated-assessment model of fossil fuel emission warming and health simultaneously will support more stringent fossil fuel and sulfur controls control. Our simulations show that a policy that adjusts fossil fuel and sulfur emissions to address both

Russell, Lynn

307

Carbon dioxide emission reduction using molten carbonate fuel cell systems  

Science Journals Connector (OSTI)

Abstract The contribution of the molten carbonate fuel cell system (MCFCs) to carbon dioxide (CO2) emission reduction in power application is analyzed. \\{MCFCs\\} can separate and concentrate CO2 emitted from traditional thermal power plants (PPs) without reducing the plant's overall energy efficiency. \\{MCFCs\\} can also be used by itself as an effective CO2 separator or concentrator by managing the anode gas stream to increase the heat utilization of the system. The CO2 separated and concentrated by \\{MCFCs\\} is most effectively captured by condensation. \\{MCFCs\\} is currently used as a CO2 separator only to a limited extent due to its high cost and relatively small scale operation. However, \\{MCFCs\\} will substantially contribute to reduce CO2 emissions in power generation applications in the near future.

Jung-Ho Wee

2014-01-01T23:59:59.000Z

308

Metal-sulfur type cell having improved positive electrode  

DOE Patents (OSTI)

An novel metal-sulfur type cell operable at a temperature of 200.degree. C. or less with an energy density of 150 Whrs/Kg or better is disclosed characterized by an organo-sulfur cathode formed from an organic-sulfur compound having the general formula, in its charged state, of (R(S).sub.y).sub.n wherein y=1 to 6; n=2 to 20; and R is one or more different aliphatic or aromatic organic moieties having 1 to 20 carbon atoms, which may include one or more oxygen, sulfur, or nitrogen heteroatoms when R comprisises one of more aromatic rings, or one or more oxygen, sulfur, nitrogen, or fluorine atoms associtated with the chain when R comprises an aliphatic chain, wherein the aliphatic group may be linear or branched, saturated or unsaturated, and wherein either the aliphatic chain or the aromatic ring may have substituted groups thereon.

Dejonghe, Lutgard C. (Berkeley, CA); Visco, Steven J. (Berkeley, CA); Mailhe, Catherine C. (Berkeley, CA); Armand, Michel B. (St. Martin D'Uriage, FR)

1989-01-01T23:59:59.000Z

309

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

310

Carbon/Sulfur Nanocomposites and Additives for High-Energy Lithium...  

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

May 2011 CarbonSulfur Nanocomposites and Additives for High-Energy Lithium Sulfur Batteries "This presentation does not contain any proprietary, confidential, or otherwise...

311

E-Print Network 3.0 - amoco sulfur recovery process Sample Search...  

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

and Medicine 80 Sulfur and oxygen isotope composition of the atmosphere in Saxony (Germany) Tichomirowa et al. Summary: ? a) Mixing processes 12;Sulfur and oxygen isotope...

312

Rules to Cut Carbon Emissions Also Reduce Other Air Pollutants A first-of-its-kind study released today by scientists at Syracuse and  

E-Print Network (OSTI)

Rules to Cut Carbon Emissions Also Reduce Other Air Pollutants A first-of-its-kind study released to the reference case. This option reduced carbon dioxide emissions from the power sector by 35 percent from 2005 to significant gains in public and environmental health. "When power plants limit carbon dioxide emissions

Mather, Patrick T.

313

Gasification combined cycle: Carbon dioxide recovery, transport, and disposal  

SciTech Connect

The objective of the project is to develop engineering evaluations of technologies for the capture, use, and disposal of carbon dioxide (CO{sub 2}). This project emphasizes CO{sub 2}-capture technologies combined with integrated gasification combined-cycle (IGCC) power systems. Complementary evaluations address CO{sub 2} transportation, CO{sub 2} use, and options for the long-term sequestering of unused CO{sub 2}. Commercially available CO{sub 2}-capture technology is providing a performance and economic baseline against which to compare innovative technologies. The intent is to provide the CO{sub 2} budget, or an {open_quotes}equivalent CO{sub 2}{close_quotes} budget, associated with each of the individual energy-cycle steps, in addition to process design capital and operating costs. The value used for the {open_quotes}equivalent CO{sub 2}{close_quotes} budget is 1 kg of CO{sub 2} per kilowatt-hour (electric). The base case is a 458-MW IGCC system that uses an air-blown Kellogg-Rust-Westinghouse agglomerating fluidized-bed gasifier, Illinois No. 6 bituminous coal feed, and in-bed sulfur removal. Mining, feed preparation, and conversion result in a net electric power production of 454 MW, with a CO{sub 2} release rate of 0.835 kg/kWhe. Two additional life-cycle energy balances for emerging technologies were considered: (1) high-temperature CO{sub 2} separation with calcium- or magnesium-based sorbents, and (2) ambient-temperature facilitated-transport polymer membranes for acid-gas removal.

Doctor, R.D.; Molburg, J.C.; Thimmapuram, P.R.; Berry, G.F.; Livengood, C.D.

1994-09-01T23:59:59.000Z

314

NETL: Carbon Dioxide 101 FAQs  

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

What are people doing now to manage CO2? What are people doing now to manage CO2? SECARB's injection operations at the Mississippi test site in Escatawpa, Mississippi SECARB's injection operations at the Mississippi test site in Escatawpa, Mississippi. A combined portfolio of carbon management options is being implemented to reduce current emission levels associated with energy production while enhancing energy security and building the technologies and knowledge base for export to other countries faced with reducing emissions. The U.S. portfolio includes: (1) use fuels with reduced carbon intensity - renewables, nuclear, and natural gas; (2) adopt more efficient technologies on both the energy demand and supply sides; and (3) use carbon capture and storage (CCS) technology. CCS is a viable emission management option

315

Resistance of biofilm-covered mortars to microbiologically influenced deterioration simulated by sulfuric acid exposure  

SciTech Connect

Following the reported success of biofilm applications on metal surfaces to inhibit microbiologically influenced corrosion, effectiveness and sustainability of E. coli DH5? biofilm on mortar surface to prevent microbiologically influenced concrete deterioration (MICD) are investigated. Experiments simulating microbial attack were carried out by exposing incrementally biofilm-covered mortar specimens to sulfuric acid solutions with pH ranging from 3 to 6. Results showed that calcium concentration in control reactors without biofilm was 23–47% higher than the reactors with biofilm-covered mortar. Formation of amorphous silica gel as an indication of early stages of acid attack was observed only on the control mortar specimens without biofilm. During acidification, the biofilm continued to grow and its thickness almost doubled from ? 30 ?m before acidification to ? 60 ?m after acidification. These results demonstrated that E. coli DH5? biofilm was able to provide a protective and sustainable barrier on mortar surfaces against medium to strong sulfuric acid attack. -- Highlights: •Effectiveness of E.coli DH5? biofilm to prevent MICD was studied. •Conditions that lead to MICD were simulated by chemical acidification. •Biofilm-covered mortar specimens were exposed to sulfuric acid solutions. •The presence of biofilm helped reduce the chemically-induced mortar deterioration. •Biofilm remained alive and continued to grow during the acidification process.

Soleimani, Sahar, E-mail: ssoleima@connect.carleton.ca; Isgor, O. Burkan, E-mail: burkan_isgor@carleton.ca; Ormeci, Banu, E-mail: banu_ormeci@carleton.ca

2013-11-15T23:59:59.000Z

316

Degradation of solid oxide fuel cell metallic interconnects in fuels containing sulfur  

SciTech Connect

Hydrogen is the main fuel for all types of fuel cells except direct methanol fuel cells. Hydrogen can be generated from all manner of fossil fuels, including coal, natural gas, diesel, gasoline, other hydrocarbons, and oxygenates (e.g., methanol, ethanol, butanol, etc.). Impurities in the fuel can cause significant performance problems and sulfur, in particular, can decrease the cell performance of fuel cells, including solid oxide fuel cells (SOFC). In the SOFC, the high (800-1000°C) operating temperature yields advantages (e.g., internal fuel reforming) and disadvantages (e.g., material selection and degradation problems). Significant progress in reducing the operating temperature of the SOFC from ~1000 ºC to ~750 ºC may allow less expensive metallic materials to be used for interconnects and as balance of plant (BOP) materials. This paper provides insight on the material performance of nickel, ferritic steels, and nickel-based alloys in fuels containing sulfur, primarily in the form of H2S, and seeks to quantify the extent of possible degradation due to sulfur in the gas stream.

Ziomek-Moroz, M.; Hawk, Jeffrey A.

2005-01-01T23:59:59.000Z

317

SULFUR POLYMER STABILIZATION/SOLIDIFICATION (SPSS) TREATABILITY OF LOS ALAMOS NATIONAL LABORATORY MERCURY WASTE.  

SciTech Connect

Brookhaven National Laboratory's Sulfur Polymer Stabilization/Solidification (SPSS) process was used to treat approximately 90kg of elemental mercury mixed waste from Los Alamos National Laboratory. Treatment was carried out in a series of eight batches using a 1 ft{sup 3} pilot-scale mixer, where mercury loading in each batch was 33.3 weight percent. Although leach performance is currently not regulated for amalgamated elemental mercury (Hg) mixed waste, Toxicity Characteristic Leach Procedure (TCLP) testing of SPSS treated elemental mercury waste indicates that leachability is readily reduced to below the TCLP limit of 200 ppb (regulatory requirement following treatment by retort for wastes containing > 260 ppb Hg), and with process optimization, to levels less than the stringent Universal Treatment Standard (UTS) limit of 25 ppb that is applied to waste containing < 260 ppm Hg. In addition, mercury-contaminated debris, consisting of primary glass and plastic containers, as well as assorted mercury thermometers, switches, and labware, was first reacted with SPSS components to stabilize the mercury contamination, then macroencapsulated in the molten SPSS product. This treatment was done by vigorous agitation of the sulfur polymer powder and the comminuted debris. Larger plastic and metal containers were reacted to stabilize internal mercury contamination, and then filled with molten sulfur polymer to encapsulate the treated product.

ADAMS,J.W.; KALB,P.D.

2001-11-01T23:59:59.000Z

318

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

319

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)

320

Reaction of titanium polonides with carbon dioxide  

SciTech Connect

It has been ascertained that heating titanium and tantalum in carbon dioxide to temperatures of 500 or 800/sup 0/C alters the composition of the gas phase, causing the advent of carbon monoxide and lowering the oxygen content. Investigation of the thermal stability of titanium polonides in a carbon dioxide medium has shown that titanium mono- and hemipolonides are decomposed at temperatures below 350/sup 0/C. The temperature dependence of the vapor pressure of polonium produced in the decomposition of these polonides in a carbon dioxide medium have been determined by a radiotensimetric method. The enthalpy of the process, calculated from this relationship, is close to the enthalpy of vaporization of elementary polonium in vacuo.

Abakumov, A.S.; Malyshev, M.L.; Reznikova, N.F.

1987-05-01T23:59:59.000Z

Note: This page contains sample records for the topic "reduce sulfur dioxide" 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

Energy use and carbon dioxide emissions in the steel sector in key developing countries  

SciTech Connect

Iron and steel production consumes enormous quantities of energy, especially in developing countries where outdated, inefficient technologies are still used to produce iron and steel. Carbon dioxide emissions from steel production, which range between 5 and 15% of total country emissions in key developing countries (Brazil, China, India, Mexico, and South Africa), will continue to grow as these countries develop and as demand for steel products such as materials, automobiles, and appliances increases. In this report, we describe the key steel processes, discuss typical energy-intensity values for these processes, review historical trends in iron and steel production by process in five key developing countries, describe the steel industry in each of the five key developing countries, present international comparisons of energy use and carbon dioxide emissions among these countries, and provide our assessment of the technical potential to reduce these emissions based on best-practice benchmarking. Using a best practice benchmark, we find that significant savings, in the range of 33% to 49% of total primary energy used to produce steel, are technically possible in these countries. Similarly, we find that the technical potential for reducing intensities of carbon dioxide emissions ranges between 26% and 49% of total carbon dioxide emissions from steel production in these countries.

Price, L.K.; Phylipsen, G.J.M.; Worrell, E.

2001-04-01T23:59:59.000Z

322

Influence of Sulfur on the Carbon Deposition in Liquid Hydrocarbon Steam Reforming over CeO2-Al2O3 supported Ni and Rh Catalysts  

SciTech Connect

This study was performed to elucidate the influence of sulfur on the carbon deposition in steam reforming of liquid hydrocarbons over CeO{sub 2}-Al{sub 2}O{sub 3} supported Ni and Rh catalysts at 800 C. The characteristics of the carbon deposits on the used catalysts after the reactions without and with sulfur were investigated by temperature-programmed oxidation (TPO), transmission electron microscopy (TEM), scanning transmission X-ray microscopy (STXM), temperature-programmed hydrogenation (TPH), X-ray absorption near edge structure (XANES), and scanning electron microscopy (SEM). Though abundant carbon deposits can accumulate on the pure CeO{sub 2}-Al{sub 2}O{sub 3} support due to fuel thermal cracking, the addition of Ni or Rh metal greatly reduced the carbon deposition in the sulfur-free reaction. The presence of sulfur increased the carbon deposition on both catalysts, which has a much more significant impact for the Ni catalyst. Carbon XANES study on the used catalysts revealed that graphitic carbon was dominant in the presence of sulfur, while oxidized carbon species (quinone-like carbon, carboxyl and carbonate) prevailed without sulfur. Meanwhile, the formation of carboxyl and carbonate more dramatically dropped on the Ni catalyst than that on the Rh catalyst. Our results strongly suggest that (I) the presence of sulfur can suppress carbon gasification and promote the formation of graphitic carbon on reforming catalysts due mainly to its poisoning effect on metals, and (II) Rh catalyst possesses stronger capability to maintain carbon gasification activity than Ni catalyst in the presence of sulfur.

C Xie; Y Chen; Y Li; X Wang; C Song

2011-12-31T23:59:59.000Z

323

Inorganic by-products in waters disinfected with chlorine dioxide  

Science Journals Connector (OSTI)

The continuing diminishing sources of fresh waters has stimulated the search for unconventional water resources, such as effluents from municipal sewage treatment plants, which can be reused for purposes of irrigation in agriculture, cooling water in industry, groundwater aquifer recharge and in the long term even for drinking water. The main problem of using effluents is the presence of pathogenic bacteria and viruses that can affect human and animal health. Therefore, disinfection has been used for many years to control and reduce waterborne diseases. At the moment, most water treatment plants use sodium hypochlorite as their primary biocide. However, the toxicity of chlorinated organic compounds produced during the treatment has led to increased interest in the use of alternative agents. One possible candidate as viable substitute of free chlorine is chlorine dioxide. Before this disinfectant can be recommended for routine use, it is imperative that its safety be assessed. In this research we have investigated the presence of chlorite and chlorate in sewage disinfected with chlorine dioxide. The effect of initial concentration of biocide and contact time was evaluated using a pilot plant fed with the effluent of a municipal treatment plant. Moreover, the influence of ClO2 generator performance was analyzed and discussed.

E. Veschetti; B. Cittadini; D. Maresca; G. Citti; M. Ottaviani

2005-01-01T23:59:59.000Z

324

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

325

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.

326

Breath is a mixture of nitrogen, oxygen, carbon dioxide, water  

E-Print Network (OSTI)

12 SCIENCE Breath is a mixture of nitrogen, oxygen, carbon dioxide, water vapour, inert gases. On the basis of proton affinity, the major constituents of air and breath (nitrogen, oxygen, carbon dioxide

327

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...

Marroquin Cabrera, Juan Carlos

2012-06-07T23:59:59.000Z

328

Graph Model for Carbon Dioxide Emissions from Metallurgical Plants  

Science Journals Connector (OSTI)

Mathematical models are presented for estimating carbon dioxide emissions from metallurgical processes. The article also presents ... in graph form to calculate transit and net emissions of carbon dioxide based o...

Yu. N. Chesnokov; V. G. Lisienko; A. V. Lapteva

2013-03-01T23:59:59.000Z

329

Worldwide, accelerating glacier loss provides independent and startling evidence that global warming is occurring1 It is now clear that the Earth is warming rapidly due to man-made emissions of carbon dioxide and other heat-trap-  

E-Print Network (OSTI)

-made emissions of carbon dioxide and other heat-trap- ping gases, which blanket the planet and cause temperatures future limits on carbon emissions. · Electricity consumers should opt for "green power" where imperative that emissions of the main heat-trapping gas, car- bon dioxide (CO2), are significantly reduced

Combes, Stacey A.

330

E-Print Network 3.0 - arterial carbon dioxide Sample Search Results  

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

reactivity. inserm-00495071... , manufactured nanoparticles, especially carbon or titanium dioxide nanoparticles, could be relevant surrogate... of carbon or titanium dioxide...

331

Coal Cleaning Using Resonance Disintegration for Mercury and Sulfur Reduction Prior to Combustion  

SciTech Connect

Coal-cleaning processes have been utilized to increase the heating value of coal by extracting ash-forming minerals in the coal. These processes involve the crushing or grinding of raw coal followed by physical separation processes, taking advantage of the density difference between carbonaceous particles and mineral particles. In addition to the desired increase in the heating value of coal, a significant reduction of the sulfur content of the coal fed to a combustion unit is effected by the removal of pyrite and other sulfides found in the mineral matter. WRI is assisting PulseWave to develop an alternate, more efficient method of liberating and separating the undesirable mineral matter from the carbonaceous matter in coal. The approach is based on PulseWave's patented resonance disintegration technology that reduces that particle size of materials by application of destructive resonance, shock waves, and vortex generating forces. Illinois No.5 coal, a Wyodak coal, and a Pittsburgh No.8 coal were processed using the resonance disintegration apparatus then subjected to conventional density separations. Initial microscopic results indicate that up to 90% of the pyrite could be liberated from the coal in the machine, but limitations in the density separations reduced overall effectiveness of contaminant removal. Approximately 30-80% of the pyritic sulfur and 30-50% of the mercury was removed from the coal. The three coals (both with and without the pyritic phase separated out) were tested in WRI's 250,000 Btu/hr Combustion Test Facility, designed to replicate a coal-fired utility boiler. The flue gases were characterized for elemental, particle bound, and total mercury in addition to sulfur. The results indicated that pre-combustion cleaning could reduce a large fraction of the mercury emissions.

Andrew Lucero

2005-04-01T23:59:59.000Z

332

The Greenness of Cities: Carbon Dioxide Emissions and Urban Development  

E-Print Network (OSTI)

carbon dioxide emissions per 1,000 cubic feet of natural gas. In this case, there is much less energy

Glaeser, Edward L.; Kahn, Matthew E.

2008-01-01T23:59:59.000Z

333

Microchannel Distillation of JP-8 Jet Fuel for Sulfur Content Reduction  

SciTech Connect

In microchannel based distillation processes, thin vapor and liquid films are contacted in small channels where mass transfer is diffusion-limited. The microchannel architecture enables improvements in distillation processes. A shorter height equivalent of a theoretical plate (HETP) and therefore a more compact distillation unit can be achieved. A microchannel distillation unit was used to produce a light fraction of JP-8 fuel with reduced sulfur content for use as feed to produce fuel-cell grade hydrogen. The HETP of the microchannel unit is discussed, as well as the effects of process conditions such as feed temperature, flow rate, and reflux ratio.

Zheng, Feng; Stenkamp, Victoria S.; TeGrotenhuis, Ward E.; Huang, Xiwen; King, David L.

2006-09-16T23:59:59.000Z

334

Low Temperature Sorbents for removal of Sulfur Compounds from fluid feed Streams  

SciTech Connect

A sorbent material is provided comprising a material reactive with sulfur, a binder unreactive with sulfur and an inert material, wherein the sorbent absorbs the sulfur at temperatures between 30 and 200 C. Sulfur absorption capacity as high as 22 weight percent has been observed with these materials.

Siriwardane, Ranjan

1999-09-30T23:59:59.000Z

335

Low Temperature Sorbents for Removal of Sulfur Compounds from Fluid Feed Streams  

DOE Patents (OSTI)

A sorbent material is provided comprising a material reactive with sulfur, a binder unreactive with sulfur and an inert material, wherein the sorbent absorbs the sulfur at temperatures between 30 and 200 C. Sulfur absorption capacity as high as 22 weight percent has been observed with these materials.

Siriwardane, Ranjani

2004-06-01T23:59:59.000Z

336

Behavior of sulfur and chlorine in coal during combustion and boiler corrosion. Final technical report, 1 September, 1992--31 August, 1993  

SciTech Connect

The goals of this project are to investigate the behavior of sulfur and chlorine during pyrolysis and combustion of Illinois coals, the chemistry and mineralogy of boiler deposits, the effects of combustion gases on boiler materials, and remedial measures to reduce the sulfur and chlorine compounds in combustion gases. Replicate determinations of chlorine and sulfur evolution during coal pyrolysis-gas combustion were conducted using a pyrolysis apparatus in conjunction with a quadrupole gas analyzer. HCl is the only gaseous chlorine species measured in combustion gases. Pyrolysis of coal IBC-109 spiked with NaCl solution shows a strong peak of HCl evolution above 700C. The absence of this peak during pyrolysis of Illinois coal indicates that little chlorine in Illinois coal occurs in the NaCl form. Evolution of sulfur during coal pyrolysis was studied; the sulfur evolution profile may be explained by the sulfur forms in coal. To determine the fate of sulfur and chlorine during combustion, a set of six samples of boiler deposits from superheater and reheater tubes of an Illinois power plant was investigated. Scanning electron microscopy shows microscopic calcium sulfate droplets on cenospheres. Superheater deposits are high in mullite, hematite, and cristobalite, whereas a reheater deposit is enriched in anhydrite. The chlorine content is very low, indicating that most of the chlorine in the feed coal is lost as volatile HCl during he combustion process. The profiles of SO{sub 2} released during combustion experiments at 825 C indicate that calcium hydroxide added to the coal has a significant effect on reducing the SO{sub 2} vapors in combustion gases.

Chou, C.L.; Hackley, K.C.; Cao, J.; Moore, D.M.; Xu, J.; Ruch, R.R. [Illinois State Geological Survey, Champaign, IL (United States); Pan, W.P.; Upchurch, M.L.; Cao, H.B. [Western Kentucky Univ., Bowling Green, KY (United States)

1993-12-31T23:59:59.000Z

337

Designed amyloid fibers as materials for selective carbon dioxide capture  

E-Print Network (OSTI)

Designed amyloid fibers as materials for selective carbon dioxide capture Dan Lia,b,c,1 , Hiroyasu demonstrate that amyloids, self-assembling protein fibers, are effective for selective carbon dioxide capture formation rate is fast enough to capture carbon dioxide by dynamic separation, undiminished by the presence

338

Array of titanium dioxide nanostructures for solar energy utilization  

DOE Patents (OSTI)

An array of titanium dioxide nanostructures for solar energy utilization includes a plurality of nanotubes, each nanotube including an outer layer coaxial with an inner layer, where the inner layer comprises p-type titanium dioxide and the outer layer comprises n-type titanium dioxide. An interface between the inner layer and the outer layer defines a p-n junction.

Qiu, Xiaofeng; Parans Paranthaman, Mariappan; Chi, Miaofang; Ivanov, Ilia N; Zhang, Zhenyu

2014-12-30T23:59:59.000Z

339

Thermal Infrared Radiation and Carbon Dioxide in the Atmosphere  

E-Print Network (OSTI)

dioxide Water vapor #12;Atmospheric composition (parts per million by volume) · Nitrogen (N2) 780Thermal Infrared Radiation and Carbon Dioxide in the Atmosphere Bill Satzer 3M Company #12;Outline,840 · Oxygen (O2) 209,460 · Argon (Ar) 9340 · Carbon dioxide (CO2) 394 · Methane (CH4) 1.79 · Ozone (O3) 0

Olver, Peter

340

World Energy Consumption and Carbon Dioxide Emissions: 1950 2050  

E-Print Network (OSTI)

-U" relation with a within- sample peak between carbon dioxide emissions (and energy use) per capita and perWorld Energy Consumption and Carbon Dioxide Emissions: 1950 Ã? 2050 Richard Schmalensee, Thomas M. Stoker, andRuth A. Judson* Emissions of carbon dioxide from combustion of fossil fuels, which may

Note: This page contains sample records for the topic "reduce sulfur dioxide" 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

Glutamate Surface Speciation on Amorphous Titanium Dioxide and  

E-Print Network (OSTI)

Glutamate Surface Speciation on Amorphous Titanium Dioxide and Hydrous Ferric Oxide D I M I T R I (HFO) and titanium dioxide exhibit similar strong attachment of many adsorbates including biomolecules on amorphous titanium dioxide. The results indicate that glutamate adsorbs on HFO as a deprotonated divalent

Sverjensky, Dimitri A.

342

System for adding sulfur to a fuel cell stack system for improved fuel cell stability  

DOE Patents (OSTI)

A system for adding sulfur to a reformate stream feeding a fuel cell stack, having a sulfur source for providing sulfur to the reformate stream and a metering device in fluid connection with the sulfur source and the reformate stream. The metering device injects sulfur from the sulfur source to the reformate stream at a predetermined rate, thereby providing a conditioned reformate stream to the fuel cell stack. The system provides a conditioned reformate stream having a predetermined sulfur concentration that gives an acceptable balance of minimal drop in initial power with the desired maximum stability of operation over prolonged periods for the fuel cell stack.

Mukerjee, Subhasish; Haltiner, Jr., Karl J; Weissman, Jeffrey G

2013-08-13T23:59:59.000Z

343

Martinez Sulfuric Acid Regeneration Plt Biomass Facility | Open Energy  

Open Energy Info (EERE)

Martinez Sulfuric Acid Regeneration Plt Biomass Facility Martinez Sulfuric Acid Regeneration Plt Biomass Facility Jump to: navigation, search Name Martinez Sulfuric Acid Regeneration Plt Biomass Facility Facility Martinez Sulfuric Acid Regeneration Plt Sector Biomass Facility Type Non-Fossil Waste Location Contra Costa County, California Coordinates 37.8534093°, -121.9017954° Loading map... {"minzoom":false,"mappingservice":"googlemaps3","type":"ROADMAP","zoom":14,"types":["ROADMAP","SATELLITE","HYBRID","TERRAIN"],"geoservice":"google","maxzoom":false,"width":"600px","height":"350px","centre":false,"title":"","label":"","icon":"","visitedicon":"","lines":[],"polygons":[],"circles":[],"rectangles":[],"copycoords":false,"static":false,"wmsoverlay":"","layers":[],"controls":["pan","zoom","type","scale","streetview"],"zoomstyle":"DEFAULT","typestyle":"DEFAULT","autoinfowindows":false,"kml":[],"gkml":[],"fusiontables":[],"resizable":false,"tilt":0,"kmlrezoom":false,"poi":true,"imageoverlays":[],"markercluster":false,"searchmarkers":"","locations":[{"text":"","title":"","link":null,"lat":37.8534093,"lon":-121.9017954,"alt":0,"address":"","icon":"","group":"","inlineLabel":"","visitedicon":""}]}

344

Diesel Emissions Control-Sulfur Effects (DECSE) Program Status  

SciTech Connect

Determine the impact of fuel sulfur levels on emission control systems that could be implemented to lower emissions of NO{sub x} and PM from on-highway trucks in the 2002-2004 time frame.

None

1999-06-29T23:59:59.000Z

345

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

346

Novel Sulfur-Tolerant Anodes for Solid Oxide Fuel Cells  

SciTech Connect

One of the unique advantages of SOFCs over other types of fuel cells is the potential for direct utilization of hydrocarbon fuels (it may involve internal reforming). Unfortunately, most hydrocarbon fuels contain sulfur, which would dramatically degrade SOFC performance at parts-per-million (ppm) levels. Low concentration of sulfur (ppm or below) is difficult to remove efficiently and cost-effectively. Therefore, knowing the exact poisoning process for state-of-the-art anode-supported SOFCs with Ni-YSZ cermet anodes, understanding the detailed anode poisoning mechanism, and developing new sulfur-tolerant anodes are essential to the promotion of SOFCs that run on hydrocarbon fuels. The effect of cell operating conditions (including temperature, H{sub 2}S concentration, cell voltage/current density, etc.) on sulfur poisoning and recovery of nickel-based anode in SOFCs was investigated. It was found that sulfur poisoning is more severe at lower temperature, higher H{sub 2}S concentration or lower cell current density (higher cell voltage). In-situ Raman spectroscopy identified the nickel sulfide formation process on the surface of a Ni-YSZ electrode and the corresponding morphology change as the sample was cooled in H{sub 2}S-containing fuel. Quantum chemical calculations predicted a new S-Ni phase diagram with a region of sulfur adsorption on Ni surfaces, corresponding to sulfur poisoning of Ni-YSZ anodes under typical SOFC operating conditions. Further, quantum chemical calculations were used to predict the adsorption energy and bond length for sulfur and hydrogen atoms on various metal surfaces. Surface modification of Ni-YSZ anode by thin Nb{sub 2}O{sub 5} coating was utilized to enhance the sulfur tolerance. A multi-cell testing system was designed and constructed which is capable of simultaneously performing electrochemical tests of 12 button cells in fuels with four different concentrations of H{sub 2}S. Through systematical study of state-of-the-art anode-supported SOFC button cells, it is seen that the long-term sulfur poisoning behavior of those cells indicate that there might be a second-stage slower degradation due to sulfur poisoning, which would last for a thousand hour or even longer. However, when using G-18 sealant from PNNL, the 2nd stage poisoning was effectively prohibited.

Lei Yang; Meilin Liu

2008-12-31T23:59:59.000Z

347

CARBON DIOXIDE AND OUR OCEAN LEGACY  

E-Print Network (OSTI)

to energy-consuming activities that burn fossil fuels. On a yearly basis, the average Ameri- can produces 22 of carbon dioxide from the atmosphere, or nearly half of the fossil fuel carbon emissions over this period sea life that depend on the health and avail- ability of these shelled organisms. At present, ocean

348

Predicting Future Atmospheric Carbon Dioxide Levels  

Science Journals Connector (OSTI)

...re-quired 5-Mhz bandwidth...interstellar plasma. For UHF frequencies of 500 Mhz, this amounts...chang-ing the atmospheric carbon dioxide...in the polar areas. Although...The shaded area indicates the...per-missible atmospheric CO2 level might...emission rates are largest between 2000...

U. Siegenthaler; H. Oeschger

1978-01-27T23:59:59.000Z

349

Synthetic fuels, carbon dioxide and climate  

Science Journals Connector (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

350

Introduction Air Quality and Nitrogen Dioxide  

E-Print Network (OSTI)

- Global update 2005. Primary sources of air pollutants include combustion products from power generationIntroduction Air Quality and Nitrogen Dioxide Air pollution can be defined as "the presence effects to man and/or the environment". (DEFRA) "Clean air is considered to be a basic requirement

351

Hydroelectric Reservoirs -the Carbon Dioxide and Methane  

E-Print Network (OSTI)

Hydroelectric Reservoirs - the Carbon Dioxide and Methane Emissions of a "Carbon Free" Energy an overview on the greenhouse gas production of hydroelectric reservoirs. The goals are to point out the main how big the greenhouse gas emissions from hydroelectric reservoirs are compared to thermo-power plants

Fischlin, Andreas

352

Low temperature fracture evaluation of plasticized sulfur paving mixtures  

E-Print Network (OSTI)

May 1985 Major Subject: Civil Engineering LOW TEMPERATURE FRACTURE EVALUATION OF PLASTICIZED SULFUR PAVING MIXTURES A Thesis by KAMYAR MAHBOUB Approved as to style and content by: Dallas N. Li tie (Chai rman of Committee) Ro e . Lytto Member... modifications to the standard ASTM procedure. These modifications were required due to the nature of plasticized sulfur mixtures and asphalt cement mixtures. The J-integral version of Paris ' law was successfully used to characterize the fatigue...

Mahboub, Kamyar

2012-06-07T23:59:59.000Z

353

Effect of fuel gas composition in chemical-looping combustion with Ni-based oxygen carriers. 1. Fate of sulfur  

SciTech Connect

Chemical-looping combustion (CLC) has been suggested among the best alternatives to reduce the economic cost of CO{sub 2} capture using fuel gas because CO{sub 2} is inherently separated in the process. For gaseous fuels, natural gas, refinery gas, or syngas from coal gasification can be used. These fuels may contain different amounts of sulfur compounds, such as H{sub 2}S and COS. An experimental investigation of the fate of sulfur during CH{sub 4} combustion in a 500 W{sub th} CLC prototype using a Ni-based oxygen carrier has been carried out. The effect on the oxygen carrier behavior and combustion efficiency of several operating conditions such as temperature and H{sub 2}S concentration has been analyzed. Nickel sulfide, Ni3S{sub 2}, was formed at all operating conditions in the fuel reactor, which produced an oxygen carrier deactivation and lower combustion efficiencies. However, the oxygen carrier recovered their initial reactivity after certain time without sulfur addition. The sulfides were transported to the air reactor where SO{sub 2} was produced as final gas product. Agglomeration problems derived from the sulfides formation were never detected during continuous operation. Considering both operational and environmental aspects, fuels with sulfur contents below 100 vppm H{sub 2}S seem to be adequate to be used in an industrial CLC plant.

Garcia-Labiano, F.; de Diego, L.F.; Gayan, P.; Adanez, J.; Abad, A.; Dueso, C. [CSIC, Zaragoza (Spain)

2009-03-15T23:59:59.000Z

354

Recent advances in lithium–sulfur batteries  

Science Journals Connector (OSTI)

Abstract Lithium–sulfur (Li–S) batteries have attracted much attention lately because they have very high theoretical specific energy (2500 Wh kg?1), five times higher than that of the commercial LiCoO2/graphite batteries. As a result, they are strong contenders for next-generation energy storage in the areas of portable electronics, electric vehicles, and storage systems for renewable energy such as wind power and solar energy. However, poor cycling life and low capacity retention are main factors limiting their commercialization. To date, a large number of electrode and electrolyte materials to address these challenges have been investigated. In this review, we present the latest fundamental studies and technological development of various nanostructured cathode materials for Li–S batteries, including their preparation approaches, structure, morphology and battery performance. Furthermore, the development of other significant components of Li–S batteries including anodes, electrolytes, additives, binders and separators are also highlighted. Not only does the intention of our review article comprise the summary of recent advances in Li–S cells, but also we cover some of our proposals for engineering of Li–S cell configurations. These systematic discussion and proposed directions can enlighten ideas and offer avenues in the rational design of durable and high performance Li–S batteries in the near future.

Lin Chen; Leon L. Shaw

2014-01-01T23:59:59.000Z

355

Heat Transfer Characteristics of Sulfur and Sulfur Diluted with Hydrogen Sulfide Flowing Through Circular Tubes  

E-Print Network (OSTI)

is called the pumping-power advantage factor, and has the value 2. 5 x 10 for sodium. The only metals having a higher value of H are 13 lithium 7 and bismuth. Lithium 7 comprises 92. 5% of natural lithium, but the cost of separating it from lithium 6...-section for thermal neutrons being 0. 130 barns. For comparison, water has an absorption cross-section of 0. 58 barns for thermal neutrons (2) . Sulfur is not activated by exposure to neutron flux in such a way as to produce a radioactive isotope which...

Stone, Porter Walwyn

1960-01-01T23:59:59.000Z

356

Linked Redox Precipitation of Sulfur and Selenium under Anaerobic Conditions by Sulfate-Reducing Bacterial Biofilms  

Science Journals Connector (OSTI)

...Influence of growth rate on susceptibility to antimicrobial...handbook of chemistry and physics, 83rd ed. CRC Press...Measurement of in situ rates of selenate removal by...Aquatic chemistry: chemical rates and equilibria in natural...was therefore shown to pass through the biofilm matrix...

Simon L. Hockin; Geoffrey M. Gadd

2003-12-01T23:59:59.000Z

357

Final Technical Report HFC Concrete: A Low-Ã?Â?Ã?Â?Ã?Â?Ã?­Ã?Â?Ã?¢Ã?Â?Ã?Â?Ã?Â?Ã?Energy, Carbon-Ã?Â?Ã?Â?Ã?Â?Ã?­Dioxide-Ã?Â?Ã?Â?Ã?Â?Ã?­Negative Solution for reducing Industrial Greenhouse Gas Emissions  

SciTech Connect

Solidia/CCSM received funding for further research and development of its Low Temperature Solidification Process (LTS), which is used to create hydrate-free concrete (HFC). LTS/HFC is a technology/materials platform that offers wide applicability in the built infrastructure. Most importantly, it provides a means of making concrete without Portland cement. Cement and concrete production is a major consumer of energy and source of industrial greenhouse gas (GHG) emissions. The primary goal of this project was to develop and commercialize a novel material, HFC, which by replacing traditional concrete and cement, reduces both energy use and GHG emissions in the built infrastructure. Traditional concrete uses Portland Cement (PC) as a binder. PC production involves calcination of limestone at {approx}1450 C, which releases significant amounts of CO{sub 2} gas to the atmosphere and consumes a large amount of energy due to the high temperature required. In contrast, HFC is a carbonate-based hydrate-free concrete (HFC) that consumes CO{sub 2} gas in its production. HFC is made by reaction of silicate minerals with CO{sub 2} at temperatures below 100 C, more than an order-of-magnitude below the temperature required to make PC. Because of this significant difference in temperature, it is estimated that we will be able to reduce energy use in the cement and concrete industry by up to 30 trillion Btu by 2020. Because of the insulating properties of HFC, we believe we will also be able to significantly reduce energy use in the Building sector, though the extent of this saving is not yet quantified. It is estimated that production of a tonne of PC-based concrete requires about 6.2 million Btu of energy and produces over 1 tonne of CO{sub 2} emissions (Choate, 2003). These can be reduced to 1.9 million Btu and 0.025 tonnes of CO{sub 2} emissions per tonne of HFC (with overall CO{sub 2}-negativity possible by increasing carbonation yield). In this way, by replacing PC-based concrete with HFC in infrastructure we can reduce energy use in concrete production by 70%, and reduce CO{sub 2} emissions by 98%; thus the potential to reduce the impact of building materials on global warming and climate change is highly significant. Low Temperature Solidification (LTS) is a breakthrough technology that enables the densification of inorganic materials via a hydrothermal process. The resulting product exhibits excellent control of chemistry and microstructure, to provide durability and mechanical performance that exceeds that of concrete or natural stone. The technology can be used in a wide range of applications including facade panels, interior tiles, roof tiles, countertops, and pre-cast concrete. Replacing traditional building materials and concrete in these applications will result in significant reduction in both energy consumption and CO{sub 2} emissions.

Dr. Larry McCandlish, Principal Investigator; Dr. Richard Riman, Co-Principal Investigator

2012-05-14T23:59:59.000Z

358

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

E-Print Network (OSTI)

water outflow of the steam turbine condenser. Due to theHigh-temperature CHP Steam expansion turbine Combined CycleNatural gas expansion turbine Steam Distribution System

Zhou, Nan

2013-01-01T23:59:59.000Z

359

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

E-Print Network (OSTI)

NG Fired CC Nuclear Power Wind Power Coal Not all of theand other Renew Solar Wind Power Hydropower Nuclear Power NGcapacity of solar and wind power increasing rapidly after

Zhou, Nan

2013-01-01T23:59:59.000Z

360

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

E-Print Network (OSTI)

coal Gas coal Fat coal Coking coal Lean coal Meagre coalCoal used for coking Natural Gas Coal used as fuel Source:

Zhou, Nan

2013-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "reduce sulfur dioxide" from the National Library of EnergyBeta (NLEBeta).
While these samples are representative of the content of NLEBeta,
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361

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

E-Print Network (OSTI)

improvements along with hydropower, renewable and nuclearreport are: Power Sector Hydropower in particular has theEfficiency Expanded Hydropower Generation Capacity

Zhou, Nan

2013-01-01T23:59:59.000Z

362

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

E-Print Network (OSTI)

as energy use per unit of gross domestic product (GDP) byas energy use per unit of gross domestic product (GDP) by

Zhou, Nan

2013-01-01T23:59:59.000Z

363

Remediation of chromium(VI) in the vadose zone: stoichiometry and kinetics of chromium(VI) reduction by sulfur dioxide  

E-Print Network (OSTI)

. The reaction was also rapid, with the half-time of about 45 minutes at pH 6 and about 16 hours at pH 7. A two-step kinetic model was developed to describe changes in concentrations of Cr(VI), S(IV), and S(V). Nonlinear regression was applied to obtain...

Ahn, Min

2004-11-15T23:59:59.000Z

364

Polyaniline-modified cetyltrimethylammonium bromide-graphene oxide-sulfur nanocomposites with enhanced performance for lithium-sulfur batteries  

Science Journals Connector (OSTI)

Conductive polymer coatings can boost the power storage capacity of lithium-sulfur batteries. We report here on the design and ... polyaniline (PANI)-modified cetyltrimethylammonium bromide (CTAB)-graphene oxide ...

Yongcai Qiu; Wanfei Li; Guizhu Li; Yuan Hou; Lisha Zhou; Hongfei Li…

2014-09-01T23:59:59.000Z

365

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

366

Conversion of the Common Food Constituent 5-Hydroxymethylfurfural into a Mutagenic and Carcinogenic Sulfuric Acid Ester in the Mouse in Vivo  

Science Journals Connector (OSTI)

Conversion of the Common Food Constituent 5-Hydroxymethylfurfural into a Mutagenic and Carcinogenic Sulfuric Acid Ester in the Mouse in Vivo ... 5-Hydroxymethylfurfural (HMF), formed by acid-catalyzed dehydration and in the Maillard reaction from reducing sugars, is found at high levels in numerous foods. ... Hydroxymethylfurfural, A Versatile Platform Chemical Made from Renewable Resources ...

Bernhard H. Monien; Heinz Frank; Albrecht Seidel; Hansruedi Glatt

2009-04-22T23:59:59.000Z

367

Synergistic capture mechanisms for alkali and sulfur species from combustion. Final report  

SciTech Connect

Experimental work was carried out on a 17 kW, 600 cm long, gas laboratory combustor, to investigate the post flame reactive capture of alkali species by kaolinite. Emphasis was on alkali/sorbent interactions occurring in flue gas at temperatures above the alkali dewpoint and on the formation of water insoluble reaction products. Time-temperature studies were carried out by injecting kaolinite at different axial points along the combustor. The effect of chlorine and sulfur on alkali capture was investigated by doping the flame with SO{sub 2} and Cl{sub 2} gases to simulate coal flame environments. Particle time and temperature history was kept as close as possible to that which would ordinarily be found in a practical boiler. Experiments designed to extract apparent initial reaction rates were carried using a narrow range, 1-2 {mu}m modal size sorbent, while, a coarse, multi size sorbent was used to investigate the governing transport mechanisms. The capture reaction has been proposed to be between alkali hydroxide and activated kaolinite, and remains so in the presence of sulfur and chlorine. The presence of sulfur reduces sodium capture by under 10% at 1300{degree}C. Larger reductions at lower temperatures are attributed to the elevated dewpoint of sodium ({approximately}850{degree}C) with subsequent reduction in sorbent residence time in the alkali gas phase domain. Chlorine reduces sodium capture by 30% across the temperature range covered by the present experiments. This result has been linked to thermodynamic equilibria between sodium hydroxide, sodium chloride and water.

Peterson, T.W.; Shadman, F.; Wendt, J.O.L.; Mwabe, P.O.

1994-02-01T23:59:59.000Z

368

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

369

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

370

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

371

A Carbon Dioxide Gas Turbine Direct Cycle with Partial Condensation for Nuclear Reactors  

SciTech Connect

A carbon dioxide gas turbine power generation system with a partial condensation cycle has been proposed for thermal and fast nuclear reactors, in which compression is done partly in the liquid phase and partly in the gas phase. This cycle achieves higher cycle efficiency than a He direct cycle mainly due to reduced compressor work of the liquid phase and of the carbon dioxide real gas effect, especially in the vicinity of the critical point. If this cycle is applied to a thermal reactor, efficiency of this cycle is about 55% at a reactor outlet temperature of 900 deg. C and pressure of 12.5 MPa, which is higher by about 10% than a typical helium direct gas turbine cycle plant (PBMR) at 900 deg. C and 8.4 MPa; this cycle also provides comparable cycle efficiency at the moderate core outlet temperature of 600 deg. C with that of the helium cycle at 900 deg. C. If this cycle is applied to a fast reactor, it is anticipated to be an alternative to liquid metal cooled fast reactors that can provide slightly higher cycle efficiency at the same core outlet temperature; it would eliminate safety problems, simplify the heat transport system and simplify plant maintenance. A passive decay heat removal system is realized by connecting a liquid carbon dioxide storage tank with the reactor vessel and by supplying carbon dioxide gasified from the tank to the core in case of depressurization event. (authors)

Yasuyoshi Kato; Takeshi Nitawaki; Yoshio Yoshizawa [Research Laboratory for Nuclear Reactors, Tokyo Institute of Technology, O-okayama, Meguro-ku, Tokyo, 152-8550 (Japan)

2002-07-01T23:59:59.000Z

372

Hybrid Sulfur Thermochemical Process Development Annual Report  

SciTech Connect

The Hybrid Sulfur (HyS) Thermochemical Process is a means of producing hydrogen via water-splitting through a combination of chemical reactions and electrochemistry. Energy is supplied to the system as high temperature heat (approximately 900 C) and electricity. Advanced nuclear reactors (Generation IV) or central solar receivers can be the source of the primary energy. Large-scale hydrogen production based on this process could be a major contributor to meeting the needs of a hydrogen economy. This project's objectives include optimization of the HyS process design, analysis of technical issues and concerns, creation of a development plan, and laboratory-scale proof-of-concept testing. The key component of the HyS Process is the SO2-depolarized electrolyzer (SDE). Studies were performed that showed that an electrolyzer operating in the range of 500-600 mV per cell can lead to an overall HyS cycle efficiency in excess of 50%, which is superior to all other currently proposed thermochemical cycles. Economic analysis indicated hydrogen production costs of approximately $1.60 per kilogram for a mature nuclear hydrogen production plant. However, in order to meet commercialization goals, the electrolyzer should be capable of operating at high current density, have a long operating lifetime , and have an acceptable capital cost. The use of proton-exchange-membrane (PEM) technology, which leverages work for the development of PEM fuel cells, was selected as the most promising route to meeting these goals. The major accomplishments of this project were the design and construction of a suitable electrolyzer test facility and the proof-of-concept testing of a PEM-based SDE.

Summers, William A.; Buckner, Melvin R.

2005-07-21T23:59:59.000Z

373

Molten iron oxysulfide as a superior sulfur sorbent. Final report, [September 1989--1993  

SciTech Connect

The studies had as original objective the analysis of conditions for using liquid iron oxysulfide as a desulfuring agent during coal gasification. Ancillary was a comparison of iron oxysulfide with lime as sorbents under conditions where lime reacts with S-bearing gases to form Ca sulfate or sulfide. Primary thrust is to determine the thermodynamic requirements for desulfurization by iron additions (e.g., taconite concentrate) during combustion in gasifiers operating at high equivalence ratios. Thermodynamic analysis of lime-oxygen-sulfur system shows why lime is injected into burners under oxidizing conditions; reducing conditions forms CaS, requiring its removal, otherwise oxidation and release of S would occur. Iron as the oxysulfide liquid has a range of stability and can be used as a desulfurizing agent, if the burner/gasifier operates in a sufficiently reducing regime (high equivalence ratio); this operating range is given and is calculable for a coal composition, temperature, stoichiometry. High moisture or hydrogen contents of the coal yield a poorer degree of desulfurization. Kinetic tests on individual iron oxide particles on substrates or Pt cups with a TGA apparatus fail to predict reaction rates within a burner. Preliminary tests on the Dynamic Containment Burner with acetylene give some promise that this system can produce the proper conditions of coal gasification for use of added iron as a sulfur sorbent.

Hepworth, M.T.

1993-03-31T23:59:59.000Z

374

Sulfur tolerant highly durable CO.sub.2 sorbents  

SciTech Connect

A sorbent for the capture of carbon dioxide from a gas stream is provided, the sorbent containing calcium oxide (CaO) and at least one refractory dopant having a Tammann temperature greater than about 530.degree. C., wherein the refractory dopant enhances resistance to sintering, thereby conserving performance of the sorbent at temperatures of at least about 530.degree. C. Also provided are doped CaO sorbents for the capture of carbon dioxide in the presence of SO.sub.2.

Smirniotis, Panagiotis G. (Cincinnati, OH); Lu, Hong (Urbana, IL)

2012-02-14T23:59:59.000Z

375

REDUCING POWER PRODUCTION COSTS BY UTILIZING PETROLEUM COKE  

SciTech Connect

A Powder River Basin subbituminous coal from the North Antelope mine and a petroleum shot coke were received from Northern States Power Company (NSP) for testing the effects of parent fuel properties on coal-coke blend grindability and evaluating the utility of petroleum coke blending as a strategy for improving electrostatic precipitator (ESP) particulate collection efficiency. Petroleum cokes are generally harder than coals, as indicated by Hardgrove grindability tests. Therefore, the weaker coal component may concentrate in the finer size fractions during the pulverizing of coal-coke blends. The possibility of a coal-coke size fractionation effect is being investigated because it may adversely affect combustion performance. Although the blending of petroleum coke with coal may adversely affect combustion performance, it may enhance ESP particulate collection efficiency. Petroleum cokes contain much higher concentrations of V relative to coals. Consequently, coke blending can significantly increase the V content of fly ash resulting from coal-coke combustion. Pentavalent vanadium oxide (V{sub 2}O{sub 5}) is a known catalyst for transforming gaseous sulfur dioxide (SO{sub 2}[g]) to gaseous sulfur trioxide (SO{sub 3}[g]). The presence of SO{sub 3}(g) strongly affects fly ash resistivity and, thus, ESP performance.

NONE

1998-09-01T23:59:59.000Z

376

Reducing power production costs by utilizing petroleum coke. Annual report  

SciTech Connect

A Powder River Basin subbituminous coal from the North Antelope mine and a petroleum shot coke were received from Northern States Power Company (NSP) for testing the effects of parent fuel properties on coal-coke blend grindability and evaluating the utility of petroleum coke blending as a strategy for improving electrostatic precipitator (ESP) particulate collection efficiency. Petroleum cokes are generally harder than coals, as indicated by Hardgrove grindability tests. Therefore, the weaker coal component may concentrate in the finer size fractions during the pulverizing of coal-coke blends. The possibility of a coal-coke size fractionation effect is being investigated because it may adversely affect combustion performance, it may enhance ESP particulate collection efficiency. Petroleum cokes contain much higher concentrations of V relative to coals. Consequently, coke blending can significantly increase the V content of fly ash resulting from coal-coke combustion. Pentavalent vanadium oxide (V{sub 2}O{sub 5}) is a known catalyst for transforming gaseous sulfur dioxide (SO{sub 2}[g]) to gaseous sulfur trioxide (SO{sub 3}[g]). The presence of SO{sub 3}(g) strongly affects fly ash resistivity and, thus, ESP performance.

Galbreath, K.C.

1998-07-01T23:59:59.000Z

377

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.

378

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

379

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

380

The urgent need for carbon dioxide sequestration  

SciTech Connect

The danger of global warming has put in question the use of fossil fuels which constitute the most abundant and most reliable energy resource. Meeting the ever growing world demand for cheap energy, while simultaneously achieving the required drastic reduction in CO{sub 2} emissions can only be accomplished by actively preventing carbon dioxide generated in the combustion of fuels from accumulating in the atmosphere, i.e. by sequestration. Sequestration is possible and economically viable and is currently the only realistic solution to the dilemma of CO{sub 2} emissions. The authors have developed a very promising approach that disposes of carbon dioxide by chemically combining it in an exothermic reaction with readily available minerals to form carbonates. The resulting carbonates are stable solids that are known to be environmentally benign and to be stable on geological time scales. This stands in contrast to most other methods that do not appear to fully solve the long term problem.

Lackner, K.S.; Butt, D.P.; Jensen, R.; Ziock, H.

1998-09-01T23:59:59.000Z

Note: This page contains sample records for the topic "reduce sulfur dioxide" from the National Library of EnergyBeta (NLEBeta).
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381

Carbon dioxide in Arctic and subarctic regions  

SciTech Connect

A three year research project was presented that would define the role of the Arctic ocean, sea ice, tundra, taiga, high latitude ponds and lakes and polar anthropogenic activity on the carbon dioxide content of the atmosphere. Due to the large physical and geographical differences between the two polar regions, a comparison of CO/sub 2/ source and sink strengths of the two areas was proposed. Research opportunities during the first year, particularly those aboard the Swedish icebreaker, YMER, provided additional confirmatory data about the natural source and sink strengths for carbon dioxide in the Arctic regions. As a result, the hypothesis that these natural sources and sinks are strong enough to significantly affect global atmospheric carbon dioxide levels is considerably strengthened. Based on the available data we calculate that the whole Arctic region is a net annual sink for about 1.1 x 10/sup 15/ g of CO/sub 2/, or the equivalent of about 5% of the annual anthropogenic input into the atmosphere. For the second year of this research effort, research on the seasonal sources and sinks of CO/sub 2/ in the Arctic will be continued. Particular attention will be paid to the seasonal sea ice zones during the freeze and thaw periods, and the tundra-taiga regions, also during the freeze and thaw periods.

Gosink, T. A.; Kelley, J. J.

1981-03-01T23:59:59.000Z

382

ADDITIVE TESTING FOR IMPROVED SULFUR RETENTION: PRELIMINARY REPORT  

SciTech Connect

The Savannah River National Laboratory is collaborating with Alfred University to evaluate the potential for additives in borosilicate glass to improve sulfur retention. This preliminary report provides further background on the incorporation of sulfur in glass and outlines the experiments that are being performed by the collaborators. A simulated waste glass composition has been selected for the experimental studies. The first phase of experimental work will evaluate the impacts of BaO, PbO, and V{sub 2}O{sub 5} at concentrations of 1.0, 2.0, and 5.0 wt % on sulfate retention in simulated high level waste borosilicate glass. The second phase of experimental work will evaluate the effects of time at the melt temperature on sulfur retention. The resulting samples will be characterized to determine the amount of sulfur remaining as well as to identify the formation of any crystalline phases. The results will be used to guide the future selection of frits and glass forming chemicals in vitrifying Department of Energy wastes containing high sulfur concentrations.

Amoroso, J.; Fox, K.

2011-09-07T23:59:59.000Z

383

Influence of Shrinkage and Swelling Properties of Coal on Geologic Sequestration of Carbon Dioxide  

SciTech Connect

The potential for enhanced methane production and geologic sequestration of carbon dioxide in coalbeds needs to be evaluated before large-scale sequestration projects are undertaken. Geologic sequestration of carbon dioxide in deep unmineable coal seams with the potential for enhanced coalbed methane production has become a viable option to reduce greenhouse gas emissions. The coal matrix is believed to shrink during methane production and swell during the injection of carbon dioxide, causing changes in tlie cleat porosity and permeability of the coal seam. However, the influence of swelling and shrinkage, and the geomechanical response during the process of carbon dioxide injection and methane recovery, are not well understood. A three-dimensional swelling and shrinkage model based on constitutive equations that account for the coupled fluid pressure-deformation behavior of a porous medium was developed and implemented in an existing reservoir model. Several reservoir simulations were performed at a field site located in the San Juan basin to investigate the influence of swelling and shrinkage, as well as other geomechanical parameters, using a modified compositional coalbed methane reservoir simulator (modified PSU-COALCOMP). The paper presents numerical results for interpretation of reservoir performance during injection of carbon dioxide at this site. Available measured data at the field site were compared with computed values. Results show that coal swelling and shrinkage during the process of enhanced coalbed methane recovery can have a significant influence on the reservoir performance. Results also show an increase in the gas production rate with an increase in the elastic modulus of the reservoir material and increase in cleat porosity. Further laboratory and field tests of the model are needed to furnish better estimates of petrophysical parameters, test the applicability of thee model, and determine the need for further refinements to the mathematical model.

Siriwardane, H.J.; Gondle, R.; Smith, D.H.

2007-05-01T23:59:59.000Z

384

Trade, transport, and sinks extend the carbon dioxide responsibility of countries: An editorial essay  

SciTech Connect

Globalization and the dynamics of ecosystem sinks need be considered in post-Kyoto climate negotiations as they increasingly affect the carbon dioxide concentration in the atmosphere. Currently, the allocation of responsibility for greenhouse gas mitigation is based on territorial emissions from fossil-fuel combustion, process emissions and some land-use emissions. However, at least three additional factors can significantly alter a country's impact on climate from carbon dioxide emissions. First, international trade causes a separation of consumption from production, reducing domestic pollution at the expense of foreign producers, or vice versa. Second, international transportation emissions are not allocated to countries for the purpose of mitigation. Third, forest growth absorbs carbon dioxide and can contribute to both carbon sequestration and climate change protection. Here we quantify how these three factors change the carbon dioxide emissions allocated to China, Japan, Russia, USA, and European Union member countries. We show that international trade can change the carbon dioxide currently allocated to countries by up to 60% and that forest expansion can turn some countries into net carbon sinks. These factors are expected to become more dominant as fossil-fuel combustion and process emissions are mitigated and as international trade and forest sinks continue to grow. Emission inventories currently in wide-spread use help to understand the global carbon cycle, but for long-term climate change mitigation a deeper understanding of the interaction between the carbon cycle and society is needed. Restructuring international trade and investment flows to meet environmental objectives, together with the inclusion of forest sinks, are crucial issues that need consideration in the design of future climate policies. And even these additional issues do not capture the full impact of changes in the carbon cycle on the global climate system.

Peters, Glen P [Center for International Climate and Energy Research (CICERO), Oslo, Norway; Marland, Gregg [ORNL; Hertwich, Edgar G. [Norwegian University of Science and Technology; Saikku, Laura [University of Helsinki

2009-01-01T23:59:59.000Z

385

Carbon Dioxide Capture from Flue Gas Using Dry Regenerable Sorbents  

SciTech Connect

Regenerable sorbents based on sodium carbonate (Na{sub 2}CO{sub 3}) can be used to separate carbon dioxide (CO{sub 2}) from coal-fired power plant flue gas. Upon thermal regeneration and condensation of water vapor, CO{sub 2} is released in a concentrated form that is suitable for reuse or sequestration. During the research project described in this report, the technical feasibility and economic viability of a thermal-swing CO{sub 2} separation process based on dry, regenerable, carbonate sorbents was confirmed. This process was designated as RTI's Dry Carbonate Process. RTI tested the Dry Carbonate Process through various research phases including thermogravimetric analysis (TGA); bench-scale fixed-bed, bench-scale fluidized-bed, bench-scale co-current downflow reactor testing; pilot-scale entrained-bed testing; and bench-scale demonstration testing with actual coal-fired flue gas. All phases of testing showed the feasibility of the process to capture greater than 90% of the CO{sub 2} present in coal-fired flue gas. Attrition-resistant sorbents were developed, and these sorbents were found to retain their CO{sub 2} removal activity through multiple cycles of adsorption and regeneration. The sodium carbonate-based sorbents developed by RTI react with CO{sub 2} and water vapor at temperatures below 80 C to form sodium bicarbonate (NaHCO3) and/or Wegscheider's salt. This reaction is reversed at temperatures greater than 120 C to release an equimolar mixture of CO{sub 2} and water vapor. After condensation of the water, a pure CO{sub 2} stream can be obtained. TGA testing showed that the Na{sub 2}CO3 sorbents react irreversibly with sulfur dioxide (SO{sub 2}) and hydrogen chloride (HCl) (at the operating conditions for this process). Trace levels of these contaminants are expected to be present in desulfurized flue gas. The sorbents did not collect detectable quantities of mercury (Hg). A process was designed for the Na{sub 2}CO{sub 3}-based sorbent that includes a co-current downflow reactor system for adsorption of CO{sub 2} and a steam-heated, hollow-screw conveyor system for regeneration of the sorbent and release of a concentrated CO{sub 2} gas stream. An economic analysis of this process (based on the U.S. Department of Energy's National Energy Technology Laboratory's [DOE/NETL's] 'Carbon Capture and Sequestration Systems Analysis Guidelines') was carried out. RTI's economic analyses indicate that installation of the Dry Carbonate Process in a 500 MW{sub e} (nominal) power plant could achieve 90% CO{sub 2} removal with an incremental capital cost of about $69 million and an increase in the cost of electricity (COE) of about 1.95 cents per kWh. This represents an increase of roughly 35.4% in the estimated COE - which compares very favorable versus MEA's COE increase of 58%. Both the incremental capital cost and the incremental COE were projected to be less than the comparable costs for an equally efficient CO{sub 2} removal system based on monoethanolamine (MEA).

Thomas Nelson; David Green; Paul Box; Raghubir Gupta; Gennar Henningsen

2007-06-30T23:59:59.000Z

386

Sulfur-Modified Zero-Valent Iron for Remediation Applications at DOE Sites - 13600  

SciTech Connect

Many DOE remediation sites have chemicals of concern that are compounds in higher oxidation states, which make them both more mobile and more toxic. The chemical reduction of these compounds both prevents the migration of these chemicals and in some cases reduces the toxicity. It has also been shown that zero-valent iron is a very effective substance to use in reducing oxygenated compounds in various treatment processes. These have included the treatment of halogenated hydrocarbons in the form volatile organic compounds used as solvents and pesticides. Zero-valent iron has also been used to reduce various oxidized metals such as chromium, arsenic, and mercury in order to immobilize them, decrease their toxicity, and prevent further transport. In addition, it has been used to immobilize or break down other non-metallic species such as selenium compounds and nitrates. Of particular interest at several DOE remediation sites is the fact that zero-valent iron is very effective in immobilizing several radioactive metals which are mobile in their oxidized states. These include both technetium and uranium. The main difficulty in using zero-valent iron has been its tendency to become inactive after relatively short periods of time. While it is advantageous to have the zero-valent iron particles as porous as possible in order to provide maximum surface area for reactions to take place, these pores can become clogged when the iron is oxidized. This is due to the fact that ferric oxide has a greater volume for a given mass than metallic iron. When the surfaces of the iron particles oxidize to ferric oxide, the pores become narrower and will eventually shut. In order to minimize the degradation of the chemical activity of the iron due to this process, a modification of zero-valent iron has been developed which prevents or slows this process, which decreases its effectiveness. It is called sulfur-modified iron, and it has been produced in high purity for applications in municipal water treatment applications. Sulfur-modified iron has been found to not only be an extremely economical treatment technology for municipal water supplies, where very large quantities of water must be treated economically, but it has also been demonstrated to immobilize technetium. It has the added benefit of eliminating several other harmful chemicals in water supplies. These include arsenic and selenium. In one large-scale evaluation study an integrated system implemented chemical reduction of nitrate with sulfur-modified iron followed by filtration for arsenic removal. The sulfur-modified iron that was used was an iron-based granular medium that has been commercially developed for the removal of nitrate, co-contaminants including uranium, vanadium and chromium, and other compounds from water. The independent study concluded that 'It is foreseen that the greatest benefit of this technology (sulfur-modified iron) is that it does not produce a costly brine stream as do the currently accepted nitrate removal technologies of ion exchange and reverse osmosis. This investigation confirmed that nitrate reduction via sulfur-modified iron is independent of the hydraulic loading rate. Future sulfur-modified iron treatment systems can be designed without restriction of the reactor vessel dimensions. Future vessels can be adapted to existing site constraints without being limited to height-to-width ratios that would exist if nitrate reduction were to depend on hydraulic loading rate'. Sulfur-modified iron was studied by the Pacific Northwest National Laboratory (PNNL) for its effectiveness in the reduction and permanent sequestration of technetium. The testing was done using Hanford Site groundwater together with sediment. The report stated, 'Under reducing conditions, TcO{sub 4} is readily reduced to TcIV, which forms highly insoluble oxides such at TcO{sub 2}.nH{sub 2}O. However, (re)oxidation of TcIV oxides can lead to remobilization. Under sulfidogenic conditions, most TcIV will be reduced and immobilized as Tc{sub 2}S{sub 7}, which is less readily re-mobilized, ev

Fogwell, Thomas W. [Fogwell Consulting, P.O. Box 20221, Piedmont, CA 94620 (United States)] [Fogwell Consulting, P.O. Box 20221, Piedmont, CA 94620 (United States); Santina, Pete [SMI-PS, Inc., 2073 Prado Vista, Lincoln, CA 95648 (United States)] [SMI-PS, Inc., 2073 Prado Vista, Lincoln, CA 95648 (United States)

2013-07-01T23:59:59.000Z

387

Income inequality and carbon dioxide emissions: The case of Chinese urban households  

Science Journals Connector (OSTI)

This paper draws on Chinese survey data to investigate variations in carbon dioxide emissions across households with different income levels. Rich households generate more emissions per capita than poor households via both their direct energy consumption and their higher expenditure on goods and services that use energy as an intermediate input. An econometric analysis confirms a positive relationship between emissions and income and establishes a slightly increasing marginal propensity to emit (MPE) over the relevant income range. The redistribution of income from rich to poor households is therefore shown to reduce aggregate household emissions, suggesting that the twin pursuits of reducing inequality and emissions can be achieved in tandem.

Jane Golley; Xin Meng

2012-01-01T23:59:59.000Z

388

Why sequence Sulfur cycling in the Frasassi aquifer?  

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

sulfur cycling in the Frasassi aquifer? sulfur cycling in the Frasassi aquifer? The terrestrial subsurface remains one of the least explored microbial habitats on earth, and is critical for understanding pollutant migration and attenuation, subsurface processes such as limestone dissolution (affecting porosity), and the search for life elsewhere in the solar system and beyond. The deep and sulfidic Frasassi aquifer (of Ancona, Italy) has emerged as a model system for studying sulfur cycling in the terrestrial subsurface, and this sequencing project has relevance for developing applications for wastewater treatment and capabilities relevant for radionuclide, metal and organic pollutant remediation that can be applied at environments at DOE subsurface sites. Principal Investigators: Jennifer Macalady, Penn State University

389

Sodium/Phosphorus-Sulfur Cells II. Phase Equilibria  

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

II. Phase Equilibria II. Phase Equilibria Title Sodium/Phosphorus-Sulfur Cells II. Phase Equilibria Publication Type Journal Article Year of Publication 1996 Authors Ridgway, Paul L., Frank R. McLarnon, and John S. Newman Journal Journal of the Electrochemistry Society Volume 143 Issue 2 Pagination 412-417 Keywords 25 ENERGY STORAGE, 36 MATERIALS SCIENCE, ALUMINIUM OXIDES, equilibrium, performance, PHASE DIAGRAMS, PHOSPHIDES, PHOSPHORUS ADDITIONS, SODIUM COMPOUNDS, SODIUM SULFIDES, SODIUM-SULFUR BATTERIES Abstract Equilibrium open-circuit cell voltage data from a sodium/{beta}{double_prime}-alumina/phosphorus-sulfur cell utilizing P/S ratios of 0, 0.143, and 0.332 and a sodium atom fraction ranging from 0 to 0.4 were interpreted to construct ternary phase diagrams of the Na-P-S ternary system at 350 and 400 C.

390

Indication of Meissner Effect in Sulfur-Substituted Strontium Ruthenates  

E-Print Network (OSTI)

Ceramic samples of Sr2RuO(4-y)Sy (y=0.03-1.2) with intended isovalent substitution of oxygen by sulfur have been synthesized and explored in the temperature range 4-300K. It is found that at a range of optimum sulfur substitution the magnetic response of ceramic samples reveals large diamagnetic signal with amplitudes approaching comparability with that of the YBCO-superconductors. Contrary to a pure ceramic Sr2RuO4, if properly optimized, the resistivity of sulfur-substituted samples has a metallic behavior except at lower temperatures where an upturn occurs. Both synthesis conditions and results of measurements are reported. The Meissner effect may point to high-temperature superconductivity.

Gulian, Armen

2011-01-01T23:59:59.000Z

391

Sulfur behavior in chemical looping combustion with NiO/Al{sub 2}O{sub 3} oxygen carrier  

SciTech Connect

Chemical looping combustion (CLC) is a novel technology where CO{sub 2} is inherently separated during combustion. Due to the existence of sulfur contaminants in the fossil fuels, the gaseous products of sulfur species and the interaction of sulfur contaminants with oxygen carrier are a big concern in the CLC practice. The reactivity of NiO/Al{sub 2}O{sub 3} oxygen carrier reduction with a gas mixture of CO/H{sub 2} and H{sub 2}S is investigated by means of a thermogravimetric analyzer (TGA) and Fourier Transform Infrared spectrum analyzer in this study. An X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and scanning electron microscope (SEM) are used to evaluate the phase characterization of reacted oxygen carrier, and the formation mechanisms of the gaseous products of sulfur species are elucidated in the process of chemical looping combustion with a gaseous fuel containing hydrogen sulfide. The results show that the rate of NiO reduction with H{sub 2}S is higher than the one with CO. There are only Ni and Ni{sub 3}S{sub 2} phases of nickel species in the fully reduced oxygen carrier, and no evidence for the existence of NiS or NiS{sub 2}. The formation of Ni{sub 3}S{sub 2} is completely reversible during the process of oxygen carrier redox. A liquid phase sintering on the external surface of reduced oxygen carriers is mainly attributed to the production of the low melting of Ni{sub 3}S{sub 2} in the nickel-based oxygen carrier reduction with a gaseous fuel containing H{sub 2}S. Due to the sintering of metallic nickel grains on the external surface of the reduced oxygen carrier, further reaction of the oxygen carrier with H{sub 2}S is constrained, and there is no increase of the sulfidation index of the reduced oxygen carrier with the cyclical reduction number. Also, a continuous operation with a syngas of carbon monoxide and hydrogen containing H{sub 2}S is carried out in a 1 kW{sub th} CLC prototype based on the nickel-based oxygen carrier, and the effect of the fuel reactor temperature on the release of gaseous products of sulfur species is investigated. (author)

Shen, Laihong; Gao, Zhengping; Wu, Jiahua; Xiao, Jun [Thermoenergy Engineering Research Institute, Southeast University, Nanjing 210096 (China)

2010-05-15T23:59:59.000Z

392

INVESTIGATION OF MIXED METAL SORBENT/CATALYSTS FOR THE SIMULTANEOUS REMOVAL OF SULFUR AND NITROGEN OXIDES  

SciTech Connect

Simultaneous removal of SO{sub 2} and NO{sub x} using a regenerable solid sorbent will constitute an important improvement over the use of separate processes for the removal of these two pollutants from stack gases and possibly eliminate several shortcomings of the individual SO{sub 2} and NO{sub x} removal operations. The work done at PETC and the DOE-funded investigation of the investigators on the sulfation and regeneration of alumina-supported cerium oxide sorbents have shown that they can perform well at relatively high temperatures (823-900 K) as regenerable desulfurization sorbents. Survey of the recent literature shows that addition of copper oxide to ceria lowers the sulfation temperature of ceria down to 773 K, sulfated ceria-based sorbents can function as selective SCR catalysts even at elevated temperatures, SO{sub 2} can be directly reduced to sulfur by CO on CuO-ceria catalysts, and ceria-based catalysts may have a potential for selective catalytic reduction of NO{sub x} by methane. These observations indicate a possibility of developing a ceria-based sorbent/catalyst which can remove both SO{sub 2} and NO{sub x} from flue gases within a relatively wide temperature window, produce significant amounts of elemental sulfur during regeneration, and use methane for the selective catalytic reduction of NO{sub x}. The objective of this research is to conduct kinetic and parametric studies of the selective catalytic reduction of NO{sub x} with NH{sub 3} and CH{sub 4} over alumina-supported cerium oxide and copper oxide-cerium oxide sorbent/catalysts; investigate SO{sub 2} removal at lower temperatures by supported copper oxide-cerium oxide sorbents; and investigate the possibility of elemental sulfur production during regeneration with CO or with CH{sub 4}-air mixtures.

Ates Akyurtlu; Jale F. Akyurtlu

2000-04-10T23:59:59.000Z

393

INVESTIGATION OF MIXED METAL SORBENT/CATALYSTS FOR THE SIMULTANEOUS REMOVAL OF SULFUR AND NITROGEN OXIDES  

SciTech Connect

Simultaneous removal of SO{sub 2} and NO{sub x} using a regenerable solid sorbent will constitute an important improvement over the use of separate processes for the removal of these two pollutants from stack gases and possibly eliminate several shortcomings of the individual SO{sub 2} and NO{sub x} removal operations. The work done at PETC and the DOE-funded research of the investigators on the sulfation and regeneration of alumina-supported cerium oxide sorbents have shown that they can perform well at relatively high temperatures (823-900 K) as regenerable desulfurization sorbents. Survey of the recent literature shows that addition of copper oxide to ceria lowers the sulfation temperature of ceria down to 773 K, sulfated ceria-based sorbents can function as selective SCR catalysts even at elevated temperatures, SO{sub 2} can be directly reduced to sulfur by CO on CuO-ceria catalysts, and ceria-based catalysts may have a potential for selective catalytic reduction of NO{sub x} by methane. These observations indicate a possibility of developing a ceria-based sorbent/catalyst which can remove both SO{sub 2} and NO{sub x} from flue gases within a relatively wide temperature window, produce significant amounts of elemental sulfur during regeneration, and use methane for the selective catalytic reduction of NO{sub x}. The objective of this research is to conduct kinetic and parametric studies of the selective catalytic reduction of NO{sub x} with NH{sub 3} and CH{sub 4} over alumina-supported cerium oxide and copper oxide-cerium oxide sorbent/catalysts; investigate SO{sub 2} removal at lower temperatures by supported copper oxide-cerium oxide sorbents; and investigate the possibility of elemental sulfur production during regeneration with CO or with CH{sub 4} air mixtures.

Ates Akyurtlu; Jale F. Akyurtlu

1999-11-30T23:59:59.000Z

394

Investigation of mixed metal sorbent/catalysts for the simultaneous removal of sulfur and nitrogen oxides  

SciTech Connect

Simultaneous removal of SO{sub 2} and NO{sub x} using a regenerable solid sorbent will constitute an important improvement over the use of separate processes for the removal of these two pollutants from stack gases and possibly eliminate several shortcomings of the individual SO{sub 2} and NO{sub x} removal operations. The work done at PETC and the DOE-funded investigation of the investigators on the sulfation and regeneration of alumina-supported cerium oxide sorbents have shown that they can perform well at relatively high temperatures (823-900 K) as regenerable desulfurization sorbents. Survey of the recent literature shows that addition of copper oxide to ceria lowers the sulfation temperature of ceria down to 773 K, sulfated ceria-based sorbents can function as selective SCR catalysts even at elevated temperatures, SO{sub 2} can be directly reduced to sulfur by CO on CuO-ceria catalysts, and ceria-based catalysts may have a potential for selective catalytic reduction of NO{sub x} by methane. These observations indicate a possibility of developing a ceria-based sorbent/catalyst which can remove both SO{sub 2} and NO{sub x} from flue gases within a relatively wide temperature window, produce significant amounts of elemental sulfur during regeneration, and use methane for the selective catalytic reduction of NO{sub x}. The objective of this research is to conduct kinetic and parametric studies of the selective catalytic reduction of NO{sub x} with NH{sub 3} and CH{sub 4} over alumina-supported cerium oxide and copper oxide-cerium oxide sorbent/catalysts; investigate SO{sub 2} removal at lower temperatures by supported copper oxide-cerium oxide sorbents; and investigate the possibility of elemental sulfur production during regeneration with CO or with CH{sub 4}-air mixtures.

Akyurtlu, A.; Akyurtlu, J.F.

1999-03-31T23:59:59.000Z

395

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

396

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

397

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

398

Extraction, separation, and analysis of high sulfur coal. Final report  

SciTech Connect

The work described in this report studies the removal of sulfur by oxidative interaction of various cupric salts with coal and also considers the possibility of removing organic sulfur by the selective interaction of supercritical ethanol with the organic coal matrix. Either one of these methods could potentially be used to pretreat coals before burning. The primary purpose of these studies is to ascertain the nature of the chemical reactions occurring, the chemical composition of the resultant products, and information on possible reaction mechanisms. This information should allow prediction of reasonable reaction conditions for the removal of organosulfur compound from coal.

Olesik, S.V.; Pekay, L.A.; Larkins, W. Jr. [comps.

1992-05-31T23:59:59.000Z

399

Extraction, separation, and analysis of high sulfur coal  

SciTech Connect

The work described in this report studies the removal of sulfur by oxidative interaction of various cupric salts with coal and also considers the possibility of removing organic sulfur by the selective interaction of supercritical ethanol with the organic coal matrix. Either one of these methods could potentially be used to pretreat coals before burning. The primary purpose of these studies is to ascertain the nature of the chemical reactions occurring, the chemical composition of the resultant products, and information on possible reaction mechanisms. This information should allow prediction of reasonable reaction conditions for the removal of organosulfur compound from coal.

Olesik, S.V.; Pekay, L.A.; Larkins, W. Jr. (comps.)

1992-05-31T23:59:59.000Z

400

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

Note: This page contains sample records for the topic "reduce sulfur dioxide" 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

Integrated Energy System with Beneficial Carbon Dioxide (CO2) Use  

SciTech Connect

To address the public concerns regarding the consequences of climate change from anthropogenic carbon dioxide (CO2) emissions, the U.S. Department of Energy National Energy Technology Laboratory (DOE-NETL) is actively funding a CO2 management program to develop technologies capable of reducing the CO2 emissions from fossil fuel power plants and other industrial facilities. Over the past decade, this program has focused on reducing the costs of carbon capture and storage technologies. Recently, DOE-NETL launched an alternative CO2 mitigation program focusing on beneficial CO2 reuse and supporting the development of technologies that mitigate emissions by converting CO2 to solid mineral form that can be utilized for enhanced oil recovery, in the manufacturing of concrete or as a benign landfill, in the production of valuable chemicals and/or fuels. This project was selected as a CO2 reuse activity which would conduct research and development (R&D) at the pilot scale via a cost-shared Cooperative Agreement number DE-FE0001099 with DOE-NETL and would utilize funds setaside by the American Recovery and Reinvestment Act (ARRA) of 2009 for Industrial Carbon Capture and Sequestration R&D,

Sun, Xiaolei; Rink, Nancy

2011-04-30T23:59:59.000Z

402

NETL: Gasification Systems - Liquid Carbon Dioxide/Coal Slurry for Feeding  

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

Feed Systems Feed Systems Liquid Carbon Dioxide/Coal Slurry for Feeding Low-Rank Coal to Gasifiers Project Number: DE-FE0007977 There is increased interest in carbon capture and storage (CCS) for future coal-based power plants, and in a CCS integrated gasification plant, relatively pure, high pressure CO2 stream(s) will be available within the power plant. Electric Power Research Institute (EPRI) aims to help reduce the cost and improve the efficiency of integrated gasification combined cycle (IGCC) with CCS by using a portion of the high purity CO2 product stream as the carrier fluid to feed low rank coal (LRC) into the gasifier. EPRI proposes to confirm the potential advantages of LRC/liquid carbon dioxide (LCO2) slurries by: Conducting plant-wide technical and economic simulations.

403

Low Cost Open-Path Instrument for Monitoring Atmospheric Carbon Dioxide at Sequestration Sites  

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

Low Cost open-path Instrument for Low Cost open-path Instrument for monItorIng atmospherIC Carbon DIoxIDe at sequestratIon sItes Background Growing concern over the effect on global climate of the buildup of greenhouse gases (GHG), particularly carbon dioxide (CO 2 ), in the atmosphere may lead to the curtailment of CO 2 emissions. One potential course of action by industry to reduce GHG emissions is the subsurface disposal of CO 2 . An important requirement of such disposal is verification that the injected gases remain in place and do not leak to the surface. Perhaps the most direct evidence of a successful sequestration project is the lack of a detectable CO 2 concentration above the background level in the air near the ground. Although measurement of CO 2 concentration can be performed, it is

404

Appendix B: CArBon dioxide CApture teChnology SheetS  

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

AdvAnced compression AdvAnced compression B-540 AdvAnced compression U.s. depArtment of energy AdvAnced cArbon dioxide cAptUre r&d progrAm: technology UpdAte, mAy 2013 novel concepts for the compression of lArge volUmes of co 2 primary project goals Southwest Research Institute (SwRI) is developing novel compression technology concepts to reduce carbon dioxide (CO 2 ) compression power requirements by 10% compared to conventional compressor designs. The basic concept is a semi-isothermal compression pro- cess where the CO 2 is continually cooled using an internal cooling jacket rather than using conventional interstage cooling. The project has completed thermodynamic (Phase I) and prototype testing (Phase II). A full-scale demonstration of a multi-stage, internally cooled

405

Pore-Level Modeling of Carbon Dioxide Infiltrating the Ocean Floor  

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

Infiltrating the Ocean Floor Infiltrating the Ocean Floor Grant S. Bromhal, Duane H. Smith, US DOE, National Energy Technology Laboratory, Morgantown, WV 26507-0880; M. Ferer, Department of Physics, West Virginia University, Morgantown, WV 26506-6315 Ocean sequestration of carbon dioxide is considered to be a potentially important method of reducing greenhouse gas emissions (US DOE, 1999). Oceans are currently the largest atmospheric carbon dioxide sink; and certainly, enough storage capacity exists in the oceans to hold all of the CO 2 that we can emit for many years. Additionally, technologies exist that allow us to pump liquid CO 2 into the oceans at depths between one and two kilometers for extended periods of time and five times that deep for shorter durations. The biggest unknown in the ocean sequestration process, however, is the fate and

406

The cost of carbon-dioxide abatement in Nigeria's energy sector  

Science Journals Connector (OSTI)

The cost of carbon dioxide abatement in Nigeria's energy sector has been estimated using MARKAL, a large-scale linear optimisation model, for the period between 1990 and the year 2030. The baseline scenario is based on the concept of the most-likely development-path in the energy system. An integrated abatement scenario is then developed by augmenting the baseline scenario with a set of abatement options: demand-side options, supply-side options, options for increased use of renewable resources, and options for increased use of the associated natural gas that is currently being flared in Nigerian oil fields. The options are assessed and ranked on the basis of their incremental costs per ton of carbon dioxide reduced. Finally, results of a sensitivity study of the model based on perturbations in energy demand growth assumptions are discussed.

F.I. Ibitoye; A.O. Adegbulugbe; J-F.K. Akinbami

1998-01-01T23:59:59.000Z

407

Polyamine-Tethered Porous Polymer Networks for Carbon Dioxide...  

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

Polyamine-Tethered Porous Polymer Networks for Carbon Dioxide Capture from Flue Gas Previous Next List Weigang Lu, Julian P. Sculley, Daqiang Yuan, Rajamani Krishna, Zhangwen Wei,...

408

Carbon Dioxide Capture and Storage Demonstration in Developing...  

Open Energy Info (EERE)

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...

409

Synthesis, Structure, and Carbon Dioxide Capture Properties of...  

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

Synthesis, Structure, and Carbon Dioxide Capture Properties of Zeolitic Imidazolate Frameworks Previous Next List Anh Phan, Christian J. Doonan, Fernando J. Uribe-Romo, Carolyn B....

410

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

411

Carbon dioxide sequestration underground laser based detection system.  

E-Print Network (OSTI)

??Carbon dioxide (CO 2) is a known greenhouse gas. Due to the burning of fossil fuels by industrial and power plants the atmospheric concentration of… (more)

Barr, Jamie Lynn.

2009-01-01T23:59:59.000Z

412

Los Alamos probes mysteries of uranium dioxide's thermal conductivity  

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

of nuclear materials into the hands of terrorists and other non-state actors. The depleted uranium dioxide crystals used for the thermal conductivity measurements were...

413

Per Capita Carbon Dioxide Emissions: Convergence or Divergence?  

Science Journals Connector (OSTI)

Understanding and considering the distribution of per capita carbon dioxide (CO2) emissions is important in designing international climate change ... incentives for participation. I evaluate historic internation...

Joseph E. Aldy

2006-04-01T23:59:59.000Z

414

Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program  

Alternative Fuels and Advanced Vehicles Data Center (EERE)

Tier 2 Vehicle and Tier 2 Vehicle and Gasoline Sulfur Program to someone by E-mail Share Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program on Facebook Tweet about Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program on Twitter Bookmark Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program on Google Bookmark Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program on Delicious Rank Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program on Digg Find More places to share Alternative Fuels Data Center: Tier 2 Vehicle and Gasoline Sulfur Program on AddThis.com... More in this section... Federal State Advanced Search All Laws & Incentives Sorted by Type Tier 2 Vehicle and Gasoline Sulfur Program

415

Sulfur Effect and Performance Recovery of a DOC + CSF + Cu-Zeolite...  

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

Sulfur Effect and Performance Recovery of a DOC + CSF + Cu-Zeolite SCR System Sulfur Effect and Performance Recovery of a DOC + CSF + Cu-Zeolite SCR System effect and performance...

416

Revisit Carbon/Sulfur Composite for Li-S Batteries. | EMSL  

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

Revisit CarbonSulfur Composite for Li-S Batteries. Revisit CarbonSulfur Composite for Li-S Batteries. Abstract: To correlate the carbon properties e.g. surface area and porous...

417

A design strategy applied to sulfur resistant lean NOx̳ automotive catalysts  

E-Print Network (OSTI)

Catalyst poisoning due to sulfur compounds derived from fuel sulfur presents a major challenge, intractable thus far, to development of many advanced technologies for automotive catalysts such as the lean NOx, trap. Under ...

Tang, Hairong

2005-01-01T23:59:59.000Z

418

System for adding sulfur to a fuel cell stack system for improved fuel cell stability  

DOE Patents (OSTI)

A system for adding sulfur to a fuel cell stack, having a reformer adapted to reform a hydrocarbon fuel stream containing sulfur contaminants, thereby providing a reformate stream having sulfur; a sulfur trap fluidly coupled downstream of the reformer for removing sulfur from the reformate stream, thereby providing a desulfurized reformate stream; and a metering device in fluid communication with the reformate stream upstream of the sulfur trap and with the desulfurized reformate stream downstream of the sulfur trap. The metering device is adapted to bypass a portion of the reformate stream to mix with the desulfurized reformate stream, thereby producing a conditioned reformate stream having a predetermined sulfur concentration that gives an acceptable balance of minimal drop in initial power with the desired maximum stability of operation over prolonged periods for the fuel cell stack.

Mukerjee, Subhasish (Pittsford, NY); Haltiner, Jr., Karl J (Fairport, NY); Weissman, Jeffrey G. (West Henrietta, NY)

2012-03-06T23:59:59.000Z

419

Ultra-Low Sulfur diesel Update & Future Light Duty Diesel | Department...  

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

Ultra-Low Sulfur diesel Update & Future Light Duty Diesel Ultra-Low Sulfur diesel Update & Future Light Duty Diesel Presentation given at DEER 2006, August 20-24, 2006, Detroit,...

420

Argonne Transportation - Engines - Reducing Heavy Vehicle Idling  

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

Reducing Vehicle Idling Reducing Vehicle Idling What is Idling? graphic of a hypothetical no-idling sign When a vehicle's engine is on but the vehicle is not in motion, it is idling. Sitting at traffic lights, waiting in a running car to pick someone up, trucks idling while their drivers make deliveries or sleep during rest stops - these are all examples of idling. Why Care About Idling? Although many individual idling episodes are small, the cumulative impacts of idling are large! Consider that idling in the United States uses more than 6 billion gallons of fuel at a cost of more than $20 billion EACH year. Add to that the costs of maintenance related to the extra engine running time and the added emissions of particulates (PM10), nitrogen oxides (NOx), carbon monoxide (CO) and carbon dioxide (CO2) related to

Note: This page contains sample records for the topic "reduce sulfur dioxide" 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

Neutron reflectometry characterization of interface width between sol-gel titanium dioxide and silicon dioxide thin films  

SciTech Connect

Neutron reflectometry (NR) was used to directly measure the interface width between a titanium dioxide and a silicon dioxide film deposited by sol-gel processing. In a bilayer heated to 450 C, NR measurements showed that the interface width is 0.8 nm. This width is the same as the roughness of a sol-gel silicon dioxide surface after the same heat treatment, suggesting no interdiffusion or mixing at the bilayer interface.

Keddie, J.L.; Norton, L.J.; Kramer, E.J.; Giannelis, E.P. (Cornell Univ., Ithaca, NY (United States). Dept. of Materials Science and Engineering)

1993-10-01T23:59:59.000Z

422

Method for extracting and sequestering carbon dioxide  

DOE Patents (OSTI)

A method and apparatus to extract and sequester carbon dioxide (CO.sub.2) from a stream or volume of gas wherein said method and apparatus hydrates CO.sub.2, 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 CO.sub.2 from a gaseous environment.

Rau, Gregory H. (Castro Valley, CA); Caldeira, Kenneth G. (Livermore, CA)

2005-05-10T23:59:59.000Z

423

Capture of carbon dioxide by hybrid sorption  

DOE Patents (OSTI)

A composition, process and system for capturing carbon dioxide from a combustion gas stream. The composition has a particulate porous support medium that has a high volume of pores, an alkaline component distributed within the pores and on the surface of the support medium, and water adsorbed on the alkaline component, wherein the proportion of water in the composition is between about 5% and about 35% by weight of the composition. The process and system contemplates contacting the sorbent and the flowing gas stream together at a temperature and for a time such that some water remains adsorbed in the alkaline component when the contact of the sorbent with the flowing gas ceases.

Srinivasachar, Srivats

2014-09-23T23:59:59.000Z

424

A Vortex Contactor for Carbon Dioxide Separations  

SciTech Connect

Many analysts identify carbon dioxide (CO2) 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) Greenhouse Gas Research and Development Programme cited separation costs from $35 to $264 per tonne of CO2 avoided for a conventional coal fired power plant utilizing existing capture technologies. Because these costs equate to a greater than 40% increase in current power generation rates, it appears obvious that a significant improvement in CO2 separation technology is required if a negative impact on the world economy is to be avoided.

Raterman, Kevin Thomas; Mc Kellar, Michael George; Turner, Terry Donald; Podgorney, Anna Kristine; Stacey, Douglas Edwin; Stokes, B.; Vranicar, J.

2001-05-01T23:59:59.000Z

425

Carbon dioxide capture and storage: Seven years after the IPCC special report  

Science Journals Connector (OSTI)

Carbon dioxide capture and storage (CCS) entails separating carbon dioxide from coal-, biomass- or gas ... or other large industrial sources, transporting the carbon dioxide by pipeline, injecting it deep undergr...

Haroon Kheshgi; Heleen de Coninck…

2012-08-01T23:59:59.000Z

426

Retrieval of ozone and nitrogen dioxide concentrations from Stratospheric Aerosol and Gas Experiment III (SAGE III)  

E-Print Network (OSTI)

Retrieval of ozone and nitrogen dioxide concentrations from Stratospheric Aerosol and Gas extinction. We retrieve ozone and nitrogen dioxide number densities and aerosol extinction from transmission), Retrieval of ozone and nitrogen dioxide concentrations from Stratospheric Aerosol and Gas Experiment III

427

6/4/2013 Page 1 of 12 Nitrogen Dioxide SOP Standard Operating Procedures  

E-Print Network (OSTI)

6/4/2013 Page 1 of 12 Nitrogen Dioxide SOP Standard Operating Procedures Nitrogen Dioxide and Nitric Oxide Print a copy and insert into your laboratory the precautions and safe handling procedures for the use of Nitrogen Dioxide

Cohen, Ronald C.

428

Satellite observations of ozone and nitrogen dioxide: from retrievals to emission estimates  

E-Print Network (OSTI)

Satellite observations of ozone and nitrogen dioxide: from retrievals to emission estimates #12 Satellite observations of ozone and nitrogen dioxide: from retrievals to emission es- timates / by Bas Subject headings: satellite retrieval / nitrogen dioxide / ozone / air pollution / emis- sion estimates

Haak, Hein

429

Sulfur-deactivated steam reforming of gasified biomass  

SciTech Connect

The effect of hydrogen sulfide on the stream reforming of methane has been studied. Methane is the most difficult component to convert by steam reforming in the mixture of hydrocarbons, which is produced in biomass gasification. Two catalysts were subjected to hydrogen sulfide levels up to 300 ppm so as to study the effect of sulfur on their deactivation. These catalysts were the C11-9-061, from United Catalyst Inc., and the HTSR1, from Haldor Topsoee. The activation energy of the sulfur-deactivated steam-reforming reaction was calculated to be 280 and 260 kJ/mol, for each catalyst, respectively. The high values most probably originate from the fact that the degree of sulfur coverage of the nickel surface is close to 1 for these experiments. Even under these severe conditions, steam reforming of methane is possible without any carbon formation. The HTSR1 catalyst exhibits a very high sulfur-free activity, resulting in a performance in the presence of hydrogen sulfide higher than that for the C11-9-061 catalyst. By using the HTSR1 catalyst, the reactor temperature can be lowered by 60 C in order to reach comparable levels of conversion.

Koningen, J.; Sjoestroem, K. [Kungl Tekniska Hoegskolan, Stockholm (Sweden)] [Kungl Tekniska Hoegskolan, Stockholm (Sweden)

1998-02-01T23:59:59.000Z

430

Effect of sulfur on heavy duty diesel engine lubricants  

SciTech Connect

Diesel engine exhaust legislation has become quite onerous for heavy duty engines. Yet, these high thermal efficiency engines continue to meet lower exhaust particulate and NOx emissions limits, due to new engine designs and the complementary engine oil performance requirements of the API service categories. In addition, the EPA has mandated changes in on-highway diesel fuel to help meet particulate emissions regulations. On October 1, 1993, when the EPA outlawed high sulfur fuels for on-highway use, the development of the API CG-4 engine oil performance specification was already in progress. All the new diesel engine tests in the category were therefore designed to run with low (< 0.05% wt.) sulfur fuel. In some engine tests, this new fuel improved some lubricant performance characteristics and degraded others. An engine oil specification for low sulfur fuel brings new challenges to developing future specifications for diesel engine oils. Both higher and lower lubricant additive treat rate products, high performance single grade oils, and formulations to meet world-wide specifications become viable. This paper discusses the results of a diesel engine oil technology that performs well with the new, low sulfur fuel in both engine tests and in the field.

Hayden, T.E. [Texaco Fuels and Lubricants Research Dept., Beacon, NY (United States)

1996-12-01T23:59:59.000Z

431

Workshop on sulfur chemistry in flue gas desulfurization  

SciTech Connect

The Flue Gas Desulfurization Workshop was held at Morgantown, West Virginia, June 7-8, 1979. The presentations dealt with the chemistry of sulfur and calcium compounds in scrubbers. DOE and EPRI programs in this area are described. Ten papers have been entered individually into EDB and ERA. (LTN)

Wallace, W.E. Jr.

1980-05-01T23:59:59.000Z

432

Sulfur tolerant molten carbonate fuel cell anode and process  

DOE Patents (OSTI)

Molten carbonate fuel cell anodes incorporating a sulfur tolerant carbon monoxide to hydrogen water-gas-shift catalyst provide in situ conversion of carbon monoxide to hydrogen for improved fuel cell operation using fuel gas mixtures of over about 10 volume percent carbon monoxide and up to about 10 ppm hydrogen sulfide.

Remick, Robert J. (Naperville, IL)

1990-01-01T23:59:59.000Z

433

Vapor phase elemental sulfur amendment for sequestering mercury in contaminated soil  

DOE Patents (OSTI)

The process of treating elemental mercury within the soil is provided by introducing into the soil a heated vapor phase of elemental sulfur. As the vapor phase of elemental sulfur cools, sulfur is precipitated within the soil and then reacts with any elemental mercury thereby producing a reaction product that is less hazardous than elemental mercury.

Looney, Brian B.; Denham, Miles E.; Jackson, Dennis G.

2014-07-08T23:59:59.000Z

434

Sulfur Impregnation on Activated Carbon Fibers through H2S Oxidation for Vapor Phase  

E-Print Network (OSTI)

Sulfur Impregnation on Activated Carbon Fibers through H2S Oxidation for Vapor Phase Mercury: Sulfur was impregnated onto activated carbon fibers ACFs through H2S oxidation catalyzed by the sorbent CE Database subject headings: Activated carbon; Sulfur; Mercury; Hydrogen sulfides; Oxidation

Borguet, Eric

435

Sulfur-induced greenhouse warming on early Mars Sarah Stewart Johnson,1  

E-Print Network (OSTI)

and 500 mbar CO2 with varying abundances of H2O and sulfur volatiles (H2S and SO2 mixing ratios of 10Ã?3Sulfur-induced greenhouse warming on early Mars Sarah Stewart Johnson,1 Michael A. Mischna,2 melting model, we obtain a high sulfur solubility, approximately 1400 ppm, in Martian mantle melts. We

Zuber, Maria

436

Carbon dioxide adsorption and methanation on ruthenium  

SciTech Connect

The adsorption and methanation of carbon dioxide on a ruthenium-silica catalyst were studied using temperature-programmed desorption (TPD) and temperature-programmed reaction (TPR). Carbon dioxide adsorption was found to be activated; CO/sub 2/ adsorption increased significantly as the temperature increased from 298 to 435 K. During adsorption, some of the CO/sub 2/ dissociated to carbon monoxide and oxygen; upon hydrogen exposure at room temperature, the oxygen reacted to water. Methanation of adsorbed CO and of adsorbed CO/sub 2/, using TPR in flowing hydrogen, yielded a CH/sub 4/ peak with a peak temperature of 459 K for both adsorbates, indicating that both reactions follow the same mechanism after adsorption. This peak temperature did not change with initial surface coverage of CO, indicating that methanation is first order in CO coverage. The desorption and reaction spectra for Ru/SiO/sub 2/ were similar to those previously obtained for Ni/SiO/sub 2/, but both CO/sub 2/ formation and CH/sub 4/ formation proceeded faster on Ru. Also, the details of CO desorption and the changes in CO/sub 2/ and CO desorptions with initial coverage were different on the two metals. 5 figures, 3 tables.

Zagli, E.; Falconer, J.L.

1981-05-01T23:59:59.000Z

437

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.

438

Carbon Dioxide Capture DOI: 10.1002/anie.200902836  

E-Print Network (OSTI)

Carbon Dioxide Capture DOI: 10.1002/anie.200902836 Highly Selective CO2 Capture in Flexible 3D Coordination Polymer Networks** Hye-Sun Choi and Myunghyun Paik Suh* Carbon dioxide capture has been warming, and the development of efficient methods for capturing CO2 from industrial flue gas has become

Paik Suh, Myunghyun

439

Carbon Dioxide Capture by Chemical Absorption: A Solvent Comparison Study  

E-Print Network (OSTI)

1 Carbon Dioxide Capture by Chemical Absorption: A Solvent Comparison Study by Anusha Kothandaraman Students #12;2 #12;3 Carbon Dioxide Capture by Chemical Absorption: A Solvent Comparison Study by Anusha with electricity generation accounting for 40% of the total1 . Carbon capture and sequestration (CCS) is one

440

Pilot Plant Study of Carbon Dioxide Capture by Aqueous Monoethanolamine  

E-Print Network (OSTI)

i Pilot Plant Study of Carbon Dioxide Capture by Aqueous Monoethanolamine Topical Report Prepared Pilot Plant Study of Carbon Dioxide Capture by Aqueous Monoethanolamine Ross Edward Dugas, M capture using monoethanolamine (MEA). MEA is an appropriate choice for a baseline study since

Rochelle, Gary T.

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


441

Exhaust Gas Sensor Based On Tin Dioxide For Automotive Application  

E-Print Network (OSTI)

Exhaust Gas Sensor Based On Tin Dioxide For Automotive Application Arthur VALLERON a,b , Christophe, Engineering Materials Department The aim of this paper is to investigate the potentialities of gas sensor based on semi-conductor for exhaust gas automotive application. The sensing element is a tin dioxide

Paris-Sud XI, Université de

442

Carbon dioxide sequestration in concrete in different curing environments  

E-Print Network (OSTI)

Carbon dioxide sequestration in concrete in different curing environments Y.-m. Chun, T.R. Naik, USA ABSTRACT: This paper summarizes the results of an investigation on carbon dioxide (CO2) sequestration in concrete. Concrete mixtures were not air entrained. Concrete mixtures were made containing

Wisconsin-Milwaukee, University of

443

Method for synthesis of titanium dioxide nanotubes using ionic liquids  

SciTech Connect

The invention is directed to a method for producing titanium dioxide nanotubes, the method comprising anodizing titanium metal in contact with an electrolytic medium containing an ionic liquid. The invention is also directed to the resulting titanium dioxide nanotubes, as well as devices incorporating the nanotubes, such as photovoltaic devices, hydrogen generation devices, and hydrogen detection devices.

Qu, Jun; Luo, Huimin; Dai, Sheng

2013-11-19T23:59:59.000Z

444

Method for Increasing Atmospheric Carbon Dioxide in Bacteriological Incubators  

Science Journals Connector (OSTI)

...Method for Increasing Atmospheric Carbon Dioxide in...Method for Increasing Atmospheric Carbon Dioxide in...experience with water-jacket incubators...that the area of water used be the maximum...does not create condensation. For culturing...was made of the recovery of Mycobacterium...

Alfred G. Karslon; Patrick E. Caskey

1969-07-01T23:59:59.000Z

445

Carbon Dioxide, Global Warming, and Michael Crichton's "State of Fear"  

E-Print Network (OSTI)

Carbon Dioxide, Global Warming, and Michael Crichton's "State of Fear" Bert W. Rust Mathematical- tioned the connection between global warming and increasing atmospheric carbon dioxide by pointing out of these plots to global warming have spilled over to the real world, inviting both praise [4, 17] and scorn [15

Rust, Bert W.

446

The surface science of titanium dioxide Ulrike Diebold*  

E-Print Network (OSTI)

The surface science of titanium dioxide Ulrike Diebold* Department of Physics, Tulane University, New Orleans, LA 70118, USA Manuscript received in final form 7 October 2002 Abstract Titanium dioxide is reviewed on the adsorption and reaction of a wide variety of inorganic molecules (H2, O2, H2O, CO, CO2, N2

Diebold, Ulrike

447

Absorption of Carbon Dioxide in Aqueous Piperazine/Methyldiethanolamine  

E-Print Network (OSTI)

Absorption of Carbon Dioxide in Aqueous Piperazine/Methyldiethanolamine Sanjay Bishnoi and Gary T dioxide absorption in 0.6 M piperazine PZ r4 M methyldiethanolamine ( )MDEA was measured in a wetted wall loading. The absorption rate did not follow pseudo first-order beha®ior except at ®ery low loading. All

Rochelle, Gary T.

448

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

449

Strong Sulfur Binding with Conducting Magneli-Phase TinO2n-1 Nanomaterials for Improving Lithium-Sulfur Batteries  

E-Print Network (OSTI)

will go through a series of soluble intermediate higher-order polysulfides (Li2S8, Li2S6, and Li2S4 of Li2S2, Li2S, and sulfur.6-8 In order to solve these challenges, there have been recent developmentsStrong Sulfur Binding with Conducting Magneli-Phase TinO2n-1 Nanomaterials for Improving Lithium-Sulfur

Cui, Yi

450

ORNL/CDIAC-143 CARBON DIOXIDE, HYDROGRAPHIC, AND CHEMICAL DATA OBTAINED DURING THE  

E-Print Network (OSTI)

Kozyr Carbon Dioxide Information Analysis Center Oak Ridge National Laboratory Oak Ridge, Tennessee, U Prepared by the Carbon Dioxide Information Analysis Center OAK RIDGE NATIONAL LABORATORY Oak Ridge

451

Faraday rotation spectroscopy of nitrogen dioxide based on a widely tunable external cavity quantum cascade laser  

E-Print Network (OSTI)

Faraday rotation spectroscopy of nitrogen dioxide based on a widely tunable external cavity quantum: Faraday Rotation Spectroscopy, external-cavity quantum cascade laser, nitrogen dioxide, trace

452

Synchrotron X-ray Studies of Super-critical Carbon Dioxide /...  

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

Synchrotron X-ray Studies of Super-critical Carbon Dioxide Reservoir Rock Interfaces Synchrotron X-ray Studies of Super-critical Carbon Dioxide Reservoir Rock Interfaces...

453

A Novel Collaboration Paradigm for Reducing Energy Consumption and Carbon Dioxide Emissions in Data Centres  

Science Journals Connector (OSTI)

......and slow. (vi) The Maintenance work plan offered in...of the execution of maintenance jobs (e.g. antivirus...diesel generators and wind turbines. These power stations...is also similar for wind turbines. The EP cannot rely......

D. Rincón; A. Agustí-Torra; J.F. Botero; F. Raspall; D. Remondo; X. Hesselbach; M.T. Beck; H. de Meer; F. Niedermeier; G. Giuliani

2013-12-01T23:59:59.000Z

454

A Novel Collaboration Paradigm for Reducing Energy Consumption and Carbon Dioxide Emissions in Data Centres  

Science Journals Connector (OSTI)

......sources is free of costs for fuel, but to be able to compensate...this can even be extended to average or even minor customers. 3...level being associated with a price and power consumption. In this...complexity and may have collateral effects (for example, UPS batteries......

D. Rincón; A. Agustí-Torra; J.F. Botero; F. Raspall; D. Remondo; X. Hesselbach; M.T. Beck; H. de Meer; F. Niedermeier; G. Giuliani

2013-12-01T23:59:59.000Z

455

A Novel Collaboration Paradigm for Reducing Energy Consumption and Carbon Dioxide Emissions in Data Centres  

Science Journals Connector (OSTI)

......if this were compensated for by a lower tariff. This document presents the basics of...panels, the sudden drop in the power feed- in has to be evened out by increasing the...sudden unpredicted surge in the power feed-in. Therefore, the decision how power generation......

D. Rincón; A. Agustí-Torra; J.F. Botero; F. Raspall; D. Remondo; X. Hesselbach; M.T. Beck; H. de Meer; F. Niedermeier; G. Giuliani

2013-12-01T23:59:59.000Z

456

Global economic potential for reducing carbon dioxide emissions from mangrove loss  

Science Journals Connector (OSTI)

...estimate of land prices for agriculture. The calibration...percentage) Saint Lucia LCA 23...farming can be much higher than agriculture. We use the Sathirathai...yr-1 )14. Additionally, agriculture and rice cultivation...

Juha Siikamäki; James N. Sanchirico; Sunny L. Jardine

2012-01-01T23:59:59.000Z

457

A Novel Collaboration Paradigm for Reducing Energy Consumption and Carbon Dioxide Emissions in Data Centres  

Science Journals Connector (OSTI)

......a sudden drop in power generation, e.g. caused by less solar radiation or wind than...volatile renewable power generation, like solar power, is present in the...case, the amount of power generation may fluctuate strongly......

D. Rincón; A. Agustí-Torra; J.F. Botero; F. Raspall; D. Remondo; X. Hesselbach; M.T. Beck; H. de Meer; F. Niedermeier; G. Giuliani

2013-12-01T23:59:59.000Z

458

A Novel Collaboration Paradigm for Reducing Energy Consumption and Carbon Dioxide Emissions in Data Centres  

Science Journals Connector (OSTI)

......Centres. Proc. 2nd Int. Conf. Energy-Efficient Computing and Networking, e-Energy '11, New York, USA, May 31June 1, pp. 110...Computing and Networking, e- Energy '11, New York, USA, May 31June 1, pp. 2130......

D. Rincón; A. Agustí-Torra; J.F. Botero; F. Raspall; D. Remondo; X. Hesselbach; M.T. Beck; H. de Meer; F. Niedermeier; G. Giuliani

2013-12-01T23:59:59.000Z

459

Understanding Brown Coal-Water Interactions to Reduce Carbon Dioxide Emissions  

Science Journals Connector (OSTI)

Victorian brown coal has a strong affinity for water. It exhibits high monolayer water capacities (MWC) and non-freezing water contents (NFW). In electricity generation, a large amount of brown coal is burnt (...

Leigh M. Clemow; W. Roy Jackson…

2002-01-01T23:59:59.000Z

460

Technologies for Reducing Carbon Dioxide Emissions from Fossil Fuel Fired Installations  

Science Journals Connector (OSTI)

All mitigation scenarios proposed to date either tend so slow down the rate of atmospheric CO2 emissions or level out the CO2 concentration in the atmosphere. A unique system has been devised which offers a metho...

M. Steinberg

1995-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "reduce sulfur dioxide" 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

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)

462

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

463

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.

464

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

465

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

466

Sulfur-tolerant anode materials for solid oxide fuel cell application  

SciTech Connect

This paper summarizes the degradation mechanisms for SOFC anodes in the presence of sulfur and recent developments in sulfur-tolerant anodes. There are two primary sulfur-degradation mechanisms for the anode materials: physical absorption of sulfur that blocks the hydrogen reaction sites, and chemical reaction that forms nickel sulfide. The sulfur-tolerant anodes are categorized into three kinds of materials: thiospinels and metal sulfides, metal cermets, and mixed ionic and electronic conductors. Each material has its own advantages and disadvantages, and the combined application of available materials to serve as different functional components in anodes through proper design may be effective to achieve a balance between stability and performance.

Gong, M. (West Virginia University, Morgantown, WV); Liu, X. (West Virginia University, Morgantown, WV); Trembly, J.; Johnson, C.

2007-06-01T23:59:59.000Z

467

Sulfur tolerant anode materials. Quarterly report, October 1--December 31, 1987  

SciTech Connect

The goal of this program is the development of a molten carbonate fuel cell (MCFC) anode which is more tolerant of sulfur contaminants in the fuel than the current state-of-the-art nickel-based anode structures. This program addresses two different but related aspects of the sulfur contamination problem. The primary aspect is concerned with the development of a sulfur tolerant electrocatalyst for the fuel oxidation reaction. A secondary issue is the development of a sulfur tolerant water-gas-shift reaction catalyst and an investigation of potential steam reforming catalysts which also have some sulfur tolerant capabilities. These two aspects are being addressed as two separate tasks.

Not Available

1988-02-01T23:59:59.000Z

468

Sulfur tolerant anode materials. Quarterly report, January 1--March 31, 1988  

SciTech Connect

The goal of this program is the development of a molten carbonate fuel cell (MCFC) anode which is more tolerant of sulfur contaminants in the fuel than the current state-of-the-art nickel-based anode structures. This program addresses two different but related aspects of the sulfur contamination problem. The primary aspect is concerned with the development of a sulfur tolerant electrocatalyst for the fuel oxidation reaction. A secondary issue is the development of a sulfur tolerant water-gas-shift reaction catalyst and an investigation of potential steam reforming catalysts which also have some sulfur tolerant capabilities. These two aspects are being addressed as two separate tasks.

Not Available

1988-05-01T23:59:59.000Z

469

Method of burning sulfur-containing fuels in a fluidized bed boiler  

DOE Patents (OSTI)

A method of burning a sulfur-containing fuel in a fluidized bed of sulfur oxide sorbent wherein the overall utilization of sulfur oxide sorbent is increased by comminuting the bed drain solids to a smaller average particle size, preferably on the order of 50 microns, and reinjecting the comminuted bed drain solids into the bed. In comminuting the bed drain solids, particles of spent sulfur sorbent contained therein are fractured thereby exposing unreacted sorbent surface. Upon reinjecting the comminuted bed drain solids into the bed, the newly-exposed unreacted sorbent surface is available for sulfur oxide sorption, thereby increasing overall sorbent utilization.

Jones, Brian C. (Windsor, CT)

1982-01-01T23:59:59.000Z

470

Flue-gas sulfur-recovery plant for a multifuel boiler  

SciTech Connect

In October 1991, a Finnish fluting mill brought on stream a flue-gas desulfurization plant with an SO{sub 2} reduction capacity of 99%. The desulfurization plant enabled the mill to discontinue the use of its sulfur burner for SO{sub 2} production. The required makeup sulfur is now obtained in the form of sulfuric acid used by the acetic acid plant, which operates in conjunction with the evaporating plant. The mill`s sulfur consumption has decreased by about 6,000 tons/year (13.2 million lb/year) because of sulfur recycling.

Miettunen, J. [Tampella Power Inc., Tampere (Finland); Aitlahti, S. [Savon Sellu Oy, Kuopio (Finland)

1993-12-01T23:59:59.000Z

471

Synthesis and development of processes for the recovery of sulfur from acid gases. Part 1, Development of a high-temperature process for removal of H{sub 2}S from coal gas using limestone -- thermodynamic and kinetic considerations; Part 2, Development of a zero-emissions process for recovery of sulfur from acid gas streams  

SciTech Connect

Limestone can be used more effectively as a sorbent for H{sub 2}S in high-temperature gas-cleaning applications if it is prevented from undergoing calcination. Sorption of H{sub 2}S by limestone is impeded by sintering of the product CaS layer. Sintering of CaS is catalyzed by CO{sub 2}, but is not affected by N{sub 2} or H{sub 2}. The kinetics of CaS sintering was determined for the temperature range 750--900{degrees}C. When hydrogen sulfide is heated above 600{degrees}C in the presence of carbon dioxide elemental sulfur is formed. The rate-limiting step of elemental sulfur formation is thermal decomposition of H{sub 2}S. Part of the hydrogen thereby produced reacts with CO{sub 2}, forming CO via the water-gas-shift reaction. The equilibrium of H{sub 2}S decomposition is therefore shifted to favor the formation of elemental sulfur. The main byproduct is COS, formed by a reaction between CO{sub 2} and H{sub 2}S that is analogous to the water-gas-shift reaction. Smaller amounts of SO{sub 2} and CS{sub 2} also form. Molybdenum disulfide is a strong catalyst for H{sub 2}S decomposition in the presence of CO{sub 2}. A process for recovery of sulfur from H{sub 2}S using this chemistry is as follows: Hydrogen sulfide is heated in a high-temperature reactor in the presence of CO{sub 2} and a suitable catalyst. The primary products of the overall reaction are S{sub 2}, CO, H{sub 2} and H{sub 2}O. Rapid quenching of the reaction mixture to roughly 600{degrees}C prevents loss Of S{sub 2} during cooling. Carbonyl sulfide is removed from the product gas by hydrolysis back to CO{sub 2} and H{sub 2}S. Unreacted CO{sub 2} and H{sub 2}S are removed from the product gas and recycled to the reactor, leaving a gas consisting chiefly of H{sub 2} and CO, which recovers the hydrogen value from the H{sub 2}S. This process is economically favorable compared to the existing sulfur-recovery technology and allows emissions of sulfur-containing gases to be controlled to very low levels.

Towler, G.P.; Lynn, S.

1993-05-01T23:59:59.000Z

472

Demand, Supply, and Price Outlook for Low-Sulfur Diesel Fuel  

Gasoline and Diesel Fuel Update (EIA)

To help ensure that sulfates in engine exhaust do not To help ensure that sulfates in engine exhaust do not prevent manufacturers of heavy-duty diesel engines from meeting new particulate emissions standards for 1994 and later model years, 1 the Clean Air Act Amend- ments of 1990 (CAAA90) require refiners to reduce the sulfur content of on-highway diesel fuel from current average levels of 0.30 percent by weight to no more than 0.05 percent by weight. The new standard, which goes into effect October 1, 1993, also requires that on-highway diesel fuel have a minimum cetane index of 40 or a maximum aromatic content of 35 percent by volume. 2 (See list of terms and definitions on the fol- lowing page.) This provision is designed to prevent any future rises in aromatics levels. 3 Since the direct mea- surement of aromatics is complex, a minimum cetane

473

In situ Observation of Sulfur in Living Mammalian Cells: Uptake of Taurine  

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

In situ Observation of Sulfur in Living In situ Observation of Sulfur in Living Mammalian Cells: Uptake of Taurine into MDCK Cells Sulfur is essential for life. It plays important roles in the amino acids methionine and cysteine, and has a structural function in disulfide bonds. As a component of iron-sulfur clusters it takes part in electron and sulfur transfer reactions.1 Glutathione, a sulfur-containing tripeptide, is an important part of biological antioxidant systems.2 Another example for the biological relevance of sulfur is the amino acid taurine, which is present in high concentrations in algae and the animal kingdom. Taurine has been implicated in a range of physiological phenomena, but its osmolytic role in cell volum