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We encourage you to perform a real-time search of NLEBeta
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1

Colorado Nonhydrocarbon Gases Removed from Natural Gas (Million...  

Annual Energy Outlook 2012 (EIA)

Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet) Colorado Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet) Decade Year-0 Year-1 Year-2 Year-3...

2

Continuous cryopump with a method for removal of solidified gases  

DOE Patents (OSTI)

An improved cryopump for the removal of gases from a high vacuum, comprising a cryopanel incorporating honeycomb structure, refrigerant means thermally connected to the cryopanel, and a rotatable channel moving azimuthally around an axis located near the center of the cryopanel, removing gases adsorbed within the honeycomb structure by subliming them and conducting them outside the vacuum vessel. 4 figs.

Carlson, L.W.; Herman, H.

1988-05-05T23:59:59.000Z

3

Other States Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic  

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

Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet) Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet) Other States Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet) Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 - - - - - - - - - - - - 1997 513 491 515 539 557 534 541 579 574 585 558 573 1998 578 536 591 581 517 456 486 486 471 477 457 468 1999 466 438 489 495 499 510 547 557 544 555 541 579 2000 587 539 605 587 615 570 653 629 591 627 609 611 2001 658 591 677 690 718 694 692 679 686 697 688 700 2002 639 591 587 621 622 605 654 639 649 650 623 638 2003 689 624 649 676 702 691 733 732 704 734 719 748 2004 741 697 727 692 692 688 718 729 706 723 711 718

4

Comparative Analysis of Alternative Means for Removing Noncondensable Gases  

Open Energy Info (EERE)

Comparative Analysis of Alternative Means for Removing Noncondensable Gases Comparative Analysis of Alternative Means for Removing Noncondensable Gases from Flashed-Steam Geothermal Power Plants:April 1999 - March 2000 Dataset Summary Description This dataset corresponds to the final report on a screening study to compare six methods of removing noncondensable gases from direct-use geo-thermal steam power plants. This report defines the study methodologies and compares the performance and economics of selected gas-removal systems. Recommendations are presented for follow-up investigations and implementation of some of the technologies discussed. The specific gas-removal methods include five vacuum system configurations using the conventional approach of evacuating gas/vapor mixtures from the power plant condenser system and a system for physical separation of steam and gases upstream of the power turbine. The study focused on flashed-steam applications, but the results apply equally well to flashed-steam and dry-steam geothermal power plant configurations. Two gas-removal options appear to offer profitable economic potential. The hybrid vacuum system configurations and the reboiler process yield positive net present value results over wide-ranging gas concentrations. The hybrid options look favorable for both low-temperature and high-temperature resource applications. The reboiler looks profitable for low-temperature resource applications for gas levels above about 20,000 parts per million by volume. A vacuum system configuration using a three-stage turbocompressor battery may be profitable for low-temperature resources, but results show that the hybrid system is more profitable. The biphase eductor alternative cannot be recommended for commercialization at this time. The report is available from NREL's publication database.

5

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

6

Illinois Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet) Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1991 0 0 0 0 0 0 0 0 0 0 0 0 1992 0 0 0 0 0 0 0 0 0 0 0 0 1993 0 0 0 0 0 0 0 0 0 0 0 0 1994 0 0 0 0 0 0 0 0 0 0 0 0 1995 0 0 0 0 0 0 0 0 0 0 0 0 1996 0 0 0 0 0 0 0 0 0 0 0 0 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0

7

Colorado Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Colorado Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Colorado Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet) Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 - - - - - - - - - - - - 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0 2009 0 0 0 0 0 0 0 0 0 0 0 0 2010 0 0 0 0 0 0 0 0 0 0 0 0 2011 NA NA NA NA NA NA NA NA NA NA NA NA

8

Colorado Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

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

Colorado Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Colorado Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet) Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 - - - - - - - - - - - - 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0 2009 0 0 0 0 0 0 0 0 0 0 0 0 2010 0 0 0 0 0 0 0 0 0 0 0 0 2011 NA NA NA NA NA NA NA NA NA NA NA NA

9

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

10

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

11

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

12

Fluid clathrate system for continuous removal of heavy noble gases from mixtures of lighter gases  

DOE Patents (OSTI)

An apparatus and method for separation of heavy noble gas in a gas volume. An apparatus and method have been devised which includes a reservoir containing an oil exhibiting a clathrate effect for heavy noble gases with a reservoir input port and the reservoir is designed to enable the input gas volume to bubble through the oil with the heavy noble gas being absorbed by the oil exhibiting a clathrate effect. The gas having reduced amounts of heavy noble gas is output from the oil reservoir, and the oil having absorbed heavy noble gas can be treated by mechanical agitation and/or heating to desorb the heavy noble gas for analysis and/or containment and allow recycling of the oil to the reservoir.

Gross, Kenneth C. (Bolingbrook, IL); Markun, Francis (Joliet, IL); Zawadzki, Mary T. (South Bend, IN)

1998-01-01T23:59:59.000Z

13

Fluid clathrate system for continuous removal of heavy noble gases from mixtures of lighter gases  

DOE Patents (OSTI)

An apparatus and method are disclosed for separation of heavy noble gas in a gas volume. An apparatus and method have been devised which includes a reservoir containing an oil exhibiting a clathrate effect for heavy noble gases with a reservoir input port and the reservoir is designed to enable the input gas volume to bubble through the oil with the heavy noble gas being absorbed by the oil exhibiting a clathrate effect. The gas having reduced amounts of heavy noble gas is output from the oil reservoir, and the oil having absorbed heavy noble gas can be treated by mechanical agitation and/or heating to desorb the heavy noble gas for analysis and/or containment and allow recycling of the oil to the reservoir. 6 figs.

Gross, K.C.; Markun, F.; Zawadzki, M.T.

1998-04-28T23:59:59.000Z

14

Biological Removal of Siloxanes from Landfill and Digester Gases  

E-Print Network (OSTI)

volatilize from waste at landfills and wastewater treatment plants (1). As a result, biogas produced, as well as an increase in maintenance costs (6, 7). The presence of VMSs in biogas is thus a challenge recommended by most equipment manufacturers for un- hindered use (6). Of all VMSs in biogas

15

,"Ohio Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)"  

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

Monthly","9/2013" Monthly","9/2013" ,"Release Date:","12/12/2013" ,"Next Release Date:","1/7/2014" ,"Excel File Name:","n9030oh2m.xls" ,"Available from Web Page:","http://tonto.eia.gov/dnav/ng/hist/n9030oh2m.htm" ,"Source:","Energy Information Administration" ,"For Help, Contact:","infoctr@eia.doe.gov" ,,"(202) 586-8800",,,"12/19/2013 6:56:25 AM" "Back to Contents","Data 1: Ohio Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" "Sourcekey","N9030OH2" "Date","Ohio Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" 33253,0 33284,0 33312,0

16

,"Tennessee Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)"  

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

Monthly","9/2013" Monthly","9/2013" ,"Release Date:","12/12/2013" ,"Next Release Date:","1/7/2014" ,"Excel File Name:","n9030tn2m.xls" ,"Available from Web Page:","http://tonto.eia.gov/dnav/ng/hist/n9030tn2m.htm" ,"Source:","Energy Information Administration" ,"For Help, Contact:","infoctr@eia.doe.gov" ,,"(202) 586-8800",,,"12/19/2013 6:56:27 AM" "Back to Contents","Data 1: Tennessee Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" "Sourcekey","N9030TN2" "Date","Tennessee Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" 33253,0 33284,0

17

,"Tennessee Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)"  

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

Annual",2010 Annual",2010 ,"Release Date:","12/12/2013" ,"Next Release Date:","1/7/2014" ,"Excel File Name:","n9030tn2a.xls" ,"Available from Web Page:","http://tonto.eia.gov/dnav/ng/hist/n9030tn2a.htm" ,"Source:","Energy Information Administration" ,"For Help, Contact:","infoctr@eia.doe.gov" ,,"(202) 586-8800",,,"12/19/2013 6:56:27 AM" "Back to Contents","Data 1: Tennessee Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" "Sourcekey","N9030TN2" "Date","Tennessee Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" 35611,0 35976,0 37802,0 38898,0

18

,"Virginia Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)"  

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

Monthly","9/2013" Monthly","9/2013" ,"Release Date:","12/12/2013" ,"Next Release Date:","1/7/2014" ,"Excel File Name:","n9030va2m.xls" ,"Available from Web Page:","http://tonto.eia.gov/dnav/ng/hist/n9030va2m.htm" ,"Source:","Energy Information Administration" ,"For Help, Contact:","infoctr@eia.doe.gov" ,,"(202) 586-8800",,,"12/19/2013 6:56:29 AM" "Back to Contents","Data 1: Virginia Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" "Sourcekey","N9030VA2" "Date","Virginia Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" 33253,0 33284,0

19

,"Pennsylvania Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)"  

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

Annual",2010 Annual",2010 ,"Release Date:","12/12/2013" ,"Next Release Date:","1/7/2014" ,"Excel File Name:","n9030pa2a.xls" ,"Available from Web Page:","http://tonto.eia.gov/dnav/ng/hist/n9030pa2a.htm" ,"Source:","Energy Information Administration" ,"For Help, Contact:","infoctr@eia.doe.gov" ,,"(202) 586-8800",,,"12/19/2013 6:56:26 AM" "Back to Contents","Data 1: Pennsylvania Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" "Sourcekey","N9030PA2" "Date","Pennsylvania Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" 35611,0 35976,0 37802,0

20

Comparative Analysis of Alternative Means for Removing Noncondensable Gases from Flashed-Steam Geothermal Power Plants  

Open Energy Info (EERE)

June 2000 * NREL/SR-550-28329 June 2000 * NREL/SR-550-28329 Martin Vorum, P.E. Englewood, Colorado Eugene A. Fritzler, P.E. Fort Morgan, Colorado Comparative Analysis of Alternative Means for Removing Noncondensable Gases from Flashed-Steam Geothermal Power Plants April 1999-March 2000 National Renewable Energy Laboratory 1617 Cole Boulevard Golden, Colorado 80401-3393 NREL is a U.S. Department of Energy Laboratory Operated by Midwest Research Institute * * * * Battelle * * * * Bechtel Contract No. DE-AC36-99-GO10337 June 2000 * NREL/SR-550-28329 Comparative Analysis of Alternative Means for Removing Noncondensable Gases from Flashed-Steam Geothermal Power Plants April 1999-March 2000 Martin Vorum, P.E. Englewood, Colorado Eugene A. Fritzler, P.E. Fort Morgan, Colorado NREL Technical Monitor: C. Kutscher

Note: This page contains sample records for the topic "gases removed increased" 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

,"South Dakota Natural Gas Nonhydrocarbon Gases Removed (MMcf)"  

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

Monthly","9/2013" Monthly","9/2013" ,"Release Date:","12/12/2013" ,"Next Release Date:","1/7/2014" ,"Excel File Name:","n9030sd2m.xls" ,"Available from Web Page:","http://tonto.eia.gov/dnav/ng/hist/n9030sd2m.htm" ,"Source:","Energy Information Administration" ,"For Help, Contact:","infoctr@eia.doe.gov" ,,"(202) 586-8800",,,"12/19/2013 6:56:26 AM" "Back to Contents","Data 1: South Dakota Natural Gas Nonhydrocarbon Gases Removed (MMcf)" "Sourcekey","N9030SD2" "Date","South Dakota Natural Gas Nonhydrocarbon Gases Removed (MMcf)" 33253,0 33284,0 33312,0 33343,0 33373,0

22

Removal of oxides of nitrogen from gases in multi-stage coal combustion  

DOE Patents (OSTI)

Polluting NO.sub.x gas values are removed from off-gas of a multi-stage coal combustion process which includes an initial carbonizing reaction, firing of char from this reaction in a fluidized bed reactor, and burning of gases from the carbonizing and fluidized bed reactions in a topping combustor having a first, fuel-rich zone and a second, fuel-lean zone. The improvement by means of which NO.sub.x gases are removed is directed to introducing NO.sub.x -free oxidizing gas such as compressor air into the second, fuel-lean zone and completing combustion with this source of oxidizing gas. Excess air fed to the fluidized bed reactor is also controlled to obtain desired stoichiometry in the first, fuel-rich zone of the topping combustor.

Mollot, Darren J. (Morgantown, WV); Bonk, Donald L. (Louisville, OH); Dowdy, Thomas E. (Orlando, FL)

1998-01-01T23:59:59.000Z

23

,"Virginia Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)"  

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

Annual",2010 Annual",2010 ,"Release Date:","12/12/2013" ,"Next Release Date:","1/7/2014" ,"Excel File Name:","n9030va2a.xls" ,"Available from Web Page:","http://tonto.eia.gov/dnav/ng/hist/n9030va2a.htm" ,"Source:","Energy Information Administration" ,"For Help, Contact:","infoctr@eia.doe.gov" ,,"(202) 586-8800",,,"12/19/2013 6:56:29 AM" "Back to Contents","Data 1: Virginia Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" "Sourcekey","N9030VA2" "Date","Virginia Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" 35611,0 35976,0 37802,0 38898,0

24

,"Pennsylvania Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)"  

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

Monthly","9/2013" Monthly","9/2013" ,"Release Date:","12/12/2013" ,"Next Release Date:","1/7/2014" ,"Excel File Name:","n9030pa2m.xls" ,"Available from Web Page:","http://tonto.eia.gov/dnav/ng/hist/n9030pa2m.htm" ,"Source:","Energy Information Administration" ,"For Help, Contact:","infoctr@eia.doe.gov" ,,"(202) 586-8800",,,"12/19/2013 6:56:26 AM" "Back to Contents","Data 1: Pennsylvania Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" "Sourcekey","N9030PA2" "Date","Pennsylvania Natural Gas Nonhydrocarbon Gases Removed (Million Cubic Feet)" 33253,0

25

Process for removal of ammonia and acid gases from contaminated waters  

DOE Patents (OSTI)

Contaminating basic gases, i.e., ammonia and acid gases, e.g., carbon dioxide, are removed from process waters or waste waters in a combined extraction and stripping process. Ammonia in the form of ammonium ion is extracted by an immiscible organic phase comprising a liquid cation exchange component, especially an organic phosphoric acid derivative, and preferably di-2-ethyl hexyl phosphoric acid, dissolved in an alkyl hydrocarbon, aryl hydrocarbon, higher alcohol, oxygenated hydrocarbon, halogenated hydrocarbon, and mixtures thereof. Concurrently, the acidic gaseous contaminants are stripped from the process or waste waters by stripping with stream, air, nitrogen, or the like. The liquid cation exchange component has the ammonia stripped therefrom by heating, and the component may be recycled to extract additional amounts of ammonia.

King, C.J.; Mackenzie, P.D.

1982-09-03T23:59:59.000Z

26

Process for removal of ammonia and acid gases from contaminated waters  

DOE Patents (OSTI)

Contaminating basic gases, i.e., ammonia, and acid gases, e.g., carbon dioxide, are removed from process waters or waste waters in a combined extraction and stripping process. Ammonia in the form of ammonium ion is extracted by an immiscible organic phase comprising a liquid cation exchange component, especially an organic phosphoric acid derivative, and preferably di-2-ethyl hexyl phosphoric acid, dissolved in an alkyl hydrocarbon, aryl hydrocarbon, higher alcohol, oxygenated hydrocarbon, halogenated hydrocarbon, and mixtures thereof. Concurrently, the acidic gaseous contaminants are stripped from the process or waste waters by stripping with steam, air, nitrogen, or the like. The liquid cation exchange component has the ammonia stripped therefrom by heating, and the component may be recycled to extract additional amounts of ammonia.

King, C. Judson (Kensington, CA); MacKenzie, Patricia D. (Berkeley, CA)

1985-01-01T23:59:59.000Z

27

Federal Offshore--Gulf of Mexico Nonhydrocarbon Gases Removed from Natural  

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

Nonhydrocarbon Gases Removed from Natural Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet) Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0 2009 0 0 0 0 0 0 0 0 0 0 0 0 2010 0 0 0 0 0 0 0 0 0 0 0 0 2011 NA NA NA NA NA NA NA NA NA NA NA NA 2012 NA NA NA NA NA NA NA NA NA NA NA NA

28

Kinetic modeling of nitric oxide removal from exhaust gases by Selective Non-Catalytic Reduction  

E-Print Network (OSTI)

for increased pressure predict a wider temperature range at which significant nitric oxide can be removed and also in the case of RAPRENOx process the levels of N20 (a by-product in the case of the RAPRENOx process) are significantly lower. The accounting...

Chenanda, Cariappa Mudappa

2012-06-07T23:59:59.000Z

29

Trichloroethene Removal From Waste Gases in Anaerobic Biotrickling Filters Through Reductive Dechlorination  

E-Print Network (OSTI)

reductive dechlorination of PCE. Environ. Sci. Technol 2003,588. Kim, J. O. Gaseous TCE and PCE removal by an activatedTsotsis, T. T. Degradation of PCE in an anaerobic waste gas

Popat, Sudeep Chandrakant

2010-01-01T23:59:59.000Z

30

Apparatus for the detection and removal of vapor phase alkali species from coal-derived gases at high temperature and pressure  

Science Journals Connector (OSTI)

A high-pressure high-temperature apparatus has been developed for the analysis of sorbents capable of removing alkali compounds to the concentration levels required by advanced coal-fired power generating systems. The reactor is capable of operating at temperatures up to 1200? C and pressures up to 2.0 MPa. A laser-based techniquephotofragment fluorescenceenables in situ analysis of the sodium content in a gas stream before and after a sorbent bed thereby determining the efficiency of the alkali removal by the various sorbents studied (typically alumino-silicate clays). The design and development of both the reactor and the laser-based analytical technique is described.

P. G. Griffin; R. J. S. Morrison; A. Campisi; B. L. Chadwick

1998-01-01T23:59:59.000Z

31

Gas Cleaning Methods for Ambient Air and Compressed Gases  

Science Journals Connector (OSTI)

Cleaning air or compressed gases in cleanroom installations requires removal of particulate and/or ... The technology used for cleaning gases for the cleanroom is derived from processes long used in ... fossil fu...

Alvin Lieberman

1992-01-01T23:59:59.000Z

32

EIA-Voluntary Reporting of Greenhouse Gases Program - What are...  

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

gases such as hydrofluorocarbons, perfluorocarbons, and sulfur hexafluoride). The Greenhouse Effect Concentrations of several important greenhouse gases have increased by about 33...

33

Regenerative process for removal of mercury and other heavy metals from gases containing H.sub.2 and/or CO  

DOE Patents (OSTI)

A method for removal of mercury from a gaseous stream containing the mercury, hydrogen and/or CO, and hydrogen sulfide and/or carbonyl sulfide in which a dispersed Cu-containing sorbent is contacted with the gaseous stream at a temperature in the range of about 25.degree. C. to about 300.degree. C. until the sorbent is spent. The spent sorbent is contacted with a desorbing gaseous stream at a temperature equal to or higher than the temperature at which the mercury adsorption is carried out, producing a regenerated sorbent and an exhaust gas comprising released mercury. The released mercury in the exhaust gas is captured using a high-capacity sorbent, such as sulfur-impregnated activated carbon, at a temperature less than about 100.degree. C. The regenerated sorbent may then be used to capture additional mercury from the mercury-containing gaseous stream.

Jadhav, Raja A. (Naperville, IL)

2009-07-07T23:59:59.000Z

34

INCREASE  

ScienceCinema (OSTI)

The Interdisciplinary Consortium for Research and Educational Access in Science and Engineering (INCREASE), assists minority-serving institutions in gaining access to world-class research facilities.

None

2013-07-22T23:59:59.000Z

35

Processes to remove acid forming gases from exhaust gases  

DOE Patents (OSTI)

The present invention relates to a process for reducing the concentration of NO in a gas, which process comprises: (A) contacting a gas sample containing NO with a gaseous oxidizing agent to oxidize the NO to NO[sub 2]; (B) contacting the gas sample of step (A) comprising NO[sub 2] with an aqueous reagent of bisulfite/sulfite and a compound selected from urea, sulfamic acid, hydrazinium ion, hydrazoic acid, nitroaniline, sulfanilamide, sulfanilic acid, mercaptopropanoic acid, mercaptosuccinic acid, cysteine or combinations thereof at between about 0 and 100 C at a pH of between about 1 and 7 for between about 0.01 and 60 sec; and (C) optionally contacting the reaction product of step (A) with conventional chemical reagents to reduce the concentrations of the organic products of the reaction in step (B) to environmentally acceptable levels. Urea or sulfamic acid are preferred, especially sulfamic acid, and step (C) is not necessary or performed. 16 figs.

Chang, S.G.

1994-09-20T23:59:59.000Z

36

Decontamination of combustion gases in fluidized bed incinerators  

DOE Patents (OSTI)

Sulfur-containing atmospheric pollutants are effectively removed from exit gas streams produced in a fluidized bed combustion system by providing a fluidized bed of particulate material, i.e. limestone and/or dolomite wherein a concentration gradient is maintained in the vertical direction. Countercurrent contacting between upwardly directed sulfur containing combustion gases and descending sorbent particulate material creates a concentration gradient across the vertical extent of the bed characterized in progressively decreasing concentration of sulfur, sulfur dioxide and like contaminants upwardly and decreasing concentration of e.g. calcium oxide, downwardly. In this manner, gases having progressively decreasing sulfur contents contact correspondingly atmospheres having progressively increasing concentrations of calcium oxide thus assuring optimum sulfur removal.

Leon, Albert M. (Mamaroneck, NY)

1982-01-01T23:59:59.000Z

37

HYBRID SELECTIVE NON-CATALYTIC REDUCTION (SNCR)/SELECTIVE CATALYTIC REDUCTION (SCR) DEMONSTRATION FOR THE REMOVAL OF NOx FROM BOILER FLUE GASES  

SciTech Connect

The U. S. Department of Energy (DOE), Electric Power Research Institute (EPRI), Pennsylvania Electric Energy Research Council, (PEERC), New York State Electric and Gas and GPU Generation, Inc. jointly funded a demonstration to determine the capabilities for Hybrid SNCR/SCR (Selective Non-Catalytic Reduction/Selective Catalytic Reduction) technology. The demonstration site was GPU Generation's Seward Unit No.5 (147MW) located in Seward Pennsylvania. The demonstration began in October of 1997 and ended in December 1998. DOE funding was provided through Grant No. DE-FG22-96PC96256 with T. J. Feeley as the Project Manager. EPRI funding was provided through agreements TC4599-001-26999 and TC4599-002-26999 with E. Hughes as the Project Manager. This project demonstrated the operation of the Hybrid SNCR/SCR NO{sub x} control process on a full-scale coal fired utility boiler. The hybrid technology was expected to provide a cost-effective method of reducing NO{sub x} while balancing capital and operation costs. An existing urea based SNCR system was modified with an expanded-duct catalyst to provide increased NO{sub x} reduction efficiency from the SNCR while producing increased ammonia slip levels to the catalyst. The catalyst was sized to reduce the ammonia slip to the air heaters to less than 2 ppm while providing equivalent NO{sub x} reductions. The project goals were to demonstrate hybrid technology is capable of achieving at least a 55% reduction in NO{sub x} emissions while maintaining less than 2ppm ammonia slip to the air heaters, maintain flyash marketability, verify the cost benefit and applicability of Hybrid post combustion technology, and reduce forced outages due to ammonium bisulfate (ABS) fouling of the air heaters. Early system limitations, due to gas temperature stratification, restricted the Hybrid NO{sub x} reduction capabilities to 48% with an ammonia slip of 6.1 mg/Nm{sup 3} (8 ppm) at the catalyst inlet. After resolving the stratification problem, the catalyst did not have sufficient activity in order to continue the planned test program. Arsenic poisoning was found to be the cause of premature catalyst deactivation.

Jerry B. Urbas

1999-05-01T23:59:59.000Z

38

Nonhydrocarbon Gases Removed from Natural Gas  

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

6-2013 6-2013 Federal Offshore Gulf of Mexico NA NA NA NA NA NA 1997-2013 Louisiana NA NA NA NA NA NA 1996-2013 New Mexico NA NA NA NA NA NA 1996-2013 Oklahoma NA NA NA NA NA NA 1996-2013 Texas NA NA NA NA NA NA 1991-2013 Wyoming NA NA NA NA NA NA 1991-2013 Other States Other States Total NA NA NA NA NA NA 1996-2013 Alabama NA NA NA NA NA NA 1991-2013 Arizona NA NA NA NA NA NA 1996-2013 Arkansas NA NA NA NA NA NA 1991-2013 California NA NA NA NA NA NA 1996-2013 Colorado NA NA NA NA NA NA 1996-2013 Florida NA NA NA NA NA NA 1996-2013 Illinois NA NA NA NA NA NA 1991-2013 Indiana NA NA NA NA NA NA 1991-2013 Kansas NA NA NA NA NA NA 1996-2013 Kentucky NA NA NA NA NA NA 1991-2013 Maryland

39

Nonhydrocarbon Gases Removed from Natural Gas  

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

661,168 718,674 721,507 836,698 867,922 761,836 1973-2012 661,168 718,674 721,507 836,698 867,922 761,836 1973-2012 Alaska 0 0 0 0 0 0 1996-2012 Federal Offshore Gulf of Mexico 0 0 0 0 0 0 1997-2012 Louisiana 0 0 0 0 1996-2010 Louisiana Onshore NA NA NA NA NA NA 2003-2012 Louisiana State Offshore NA NA NA NA NA NA 2003-2012 New Mexico 28,962 32,444 33,997 40,191 39,333 38,358 1980-2012 Oklahoma 0 0 0 0 1996-2010 Texas 254,337 241,626 240,533 279,981 284,557 183,118 1980-2012 Texas Onshore 254,337 241,626 240,533 279,981 284,557 183,118 1992-2012 Texas State Offshore NA 0 0 0 0 0 2003-2012 Wyoming 154,157 161,952 155,366 164,221 152,421 151,288 1980-2012 Other States Other States Total 223,711 282,651 291,611 352,304 1994-2010 Alabama 16,529 17,394 16,658 14,418 18,972 NA 1980-2012

40

Nonhydrocarbon Gases Removed from Natural Gas (Summary)  

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

1-2013 1-2013 Alaska NA NA NA NA NA NA 1996-2013 Arizona NA NA NA NA NA NA 1996-2013 Arkansas NA NA NA NA NA NA 1991-2013 California NA NA NA NA NA NA 1996-2013 Colorado NA NA NA NA NA NA 1996-2013 Florida NA NA NA NA NA NA 1996-2013 Illinois NA NA NA NA NA NA 1991-2013 Indiana NA NA NA NA NA NA 1991-2013 Kansas NA NA NA NA NA NA 1996-2013 Kentucky NA NA NA NA NA NA 1991-2013 Louisiana NA NA NA NA NA NA 1996-2013 Maryland NA NA NA NA NA NA 1991-2013 Michigan NA NA NA NA NA NA 1996-2013 Mississippi NA NA NA NA NA NA 1991-2013 Missouri NA NA NA NA NA NA 1991-2013 Montana NA NA NA NA NA NA 1996-2013 Nebraska NA NA NA NA NA NA 1991-2013 Nevada NA NA NA NA NA NA 1991-2013 New Mexico NA NA NA NA NA NA 1996-2013

Note: This page contains sample records for the topic "gases removed increased" 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

Separation of polar gases from nonpolar gases  

DOE Patents (OSTI)

Polar gases such as hydrogen sulfide, sulfur dioxide and ammonia may be separated from nonpolar gases such as methane, nitrogen, hydrogen or carbon dioxide by passing a mixture of polar and nonpolar gases over the face of a multicomponent membrane at separation conditions. The multicomponent membrane which is used to effect the separation will comprise a mixture of a glycol plasticizer having a molecular weight of from about 200 to about 600 and an organic polymer cast on a porous support. The use of such membranes as exemplified by polyethylene glycol and silicon rubber composited on polysulfone will permit greater selectivity accompanied by a high flux rate in the separation process.

Kulprathipanja, S.; Kulkarni, S.S.

1986-08-26T23:59:59.000Z

42

Separation of polar gases from nonpolar gases  

DOE Patents (OSTI)

Polar gases such as hydrogen sulfide, sulfur dioxide and ammonia may be separated from nonpolar gases such as methane, nitrogen, hydrogen or carbon dioxide by passing a mixture of polar and nonpolar gases over the face of a multicomponent membrane at separation conditions. The multicomponent membrane which is used to effect the separation will comprise a mixture of a glycol plasticizer having a molecular weight of from about 200 to about 600 and an organic polymer cast on a porous support. The use of such membranes as exemplified by polyethylene glycol and silicon rubber composited on polysulfone will permit greater selectivity accompanied by a high flux rate in the separation process.

Kulprathipanja, Santi (Hoffman Estates, IL); Kulkarni, Sudhir S. (Hoffman Estates, IL)

1986-01-01T23:59:59.000Z

43

Increasing cellulose accessibility is more important than removing lignin: A comparison of cellulose solventbased lignocellulose fractionation and soaking in aqueous ammonia  

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

Increasing Increasing Cellulose Accessibility Is More Important Than Removing Lignin: A Comparison of Cellulose Solvent-Based Lignocellulose Fractionation and Soaking in Aqueous Ammonia Joseph A. Rollin, 1 Zhiguang Zhu, 1 Noppadon Sathitsuksanoh, 1,2 Y.-H. Percival Zhang 1,2,3 1 Biological Systems Engineering Department, Virginia Polytechnic Institute and State University, 210-A Seitz Hall, Blacksburg, Virginia 24061; telephone: 1-540-231-7414; fax: þ1- 540-231-3199; e-mail: ypzhang@vt.edu 2 Institute for Critical Technology and Applied Sciences (ICTAS), Virginia Polytechnic Institute and State University, Blacksburg, Virginia 3 DOE BioEnergy Science Center (BESC), Oak Ridge, Tennessee Received 18 May 2010; revision received 11 August 2010; accepted 17 August 2010 Published online 1 September 2010 in Wiley Online Library (wileyonlinelibrary.com). DOI 10.1002/bit.22919

44

Method for enhancing microbial utilization rates of gases using perfluorocarbons  

DOE Patents (OSTI)

A method of enhancing the bacterial reduction of industrial gases using perfluorocarbons (PFCs) is disclosed. Because perfluorocarbons (PFCs) allow for a much greater solubility of gases than water does, PFCs have the potential to deliver gases in higher concentrations to microorganisms when used as an additive to microbial growth media thereby increasing the rate of the industrial gas conversion to economically viable chemicals and gases.

Turick, Charles E. (Idaho Falls, ID)

1997-01-01T23:59:59.000Z

45

Technologies for Boron Removal  

Science Journals Connector (OSTI)

Tests were performed to examine the removal of boron from aqueous solution either with polyvinyl alcohol (PVA) alone or by both PVA and other inorganic additives under room temperature. ... Added calcium hydroxide increased the co-removal of borate with PVA, and this offers a polishing treatment after borate removal by liming. ... As boron removal can be achieved by chemical precipitation and coagulation, it is logical to assume that the EC could remove boron from water and industrial effluent. ...

Yonglan Xu; Jia-Qian Jiang

2007-11-23T23:59:59.000Z

46

Strongly interacting Fermi gases  

E-Print Network (OSTI)

Strongly interacting gases of ultracold fermions have become an amazingly rich test-bed for many-body theories of fermionic matter. Here we present our recent experiments on these systems. Firstly, we discuss high-precision ...

Bakr, W.

47

Method of converting environmentally pollutant waste gases to methanol  

SciTech Connect

A continuous flow method is described of converting environmentally pollutant by-product gases emitted during the manufacture of silicon carbide to methanol comprising: (a) operating a plurality of batch furnaces of a silicon carbide manufacturing plant thereby producing silicon carbide and emitting by-product gases during the operation of the furnaces; (b) staggering the operation of the batch furnaces to achieve a continuous emission of the by-product gases; (c) continuously flowing the by-product gases as emitted from the batch furnaces directly to a methanol manufacturing plant; (d) cleansing the by-product gases of particulate matter, including removing the element sulfur from the by-product gases, as they are flowed to the methanol manufacturing plant, sufficiently for use of the by-product gases in producing methanol; and (e) immediately producing methanol from the by-product gases at the methanol manufacturing plant whereby the producing of silicon carbide is joined with the producing of methanol as a unified process.

Pfingstl, H.; Martyniuk, W.; Hennepin, A. Ill; McNally, T.; Myers, R.; Eberle, L.

1993-08-03T23:59:59.000Z

48

Semi-Continuous Detection of Mercury in Gases  

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

Continuous Detection of Mercury in Gases Continuous Detection of Mercury in Gases Opportunity Research is currently active on the patented technology "Semi-Continuous Detection of Mercury in Gases." The technology, which is a spinoff of the National Energy Technology Laboratory's (NETL) GP-254 Process (U.S. patent 6,576,092), is available for licensing and/or further collaborative research from the U.S. Department of Energy's NETL. Overview This invention discloses a method for the quantitative detection of heavy metals, especially mercury, in effluent gas streams. The method employs photo-deposition and an array of surface acoustic wave sensors where each sensor monitors a specific metal. The U.S. Environmental Protection Agency issued a national regulation for mercury removal from coal-derived flue and fuel gases in December 2011,

49

California Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic  

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

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 71 76 80 78 78 76 80 79 77 79 78 80 1997 20 18 20 20 20 20 20 20 20 20 20 20 1998 62 56 62 60 62 60 62 62 60 62 60 62 1999 18 16 18 17 18 17 18 18 17 18 17 18 2000 22 20 22 22 22 22 22 22 22 22 22 22 2001 21 19 21 20 21 20 21 21 20 21 20 21 2002 224 203 227 211 219 217 217 410 274 304 330 299 2003 309 277 304 289 307 293 298 285 279 281 276 281 2004 284 260 273 270 278 269 278 275 270 279 272 277 2005 104 250 276 272 280 267 282 289 280 288 281 283 2006 277 256 293 283 293 280 283 286 269 284 275 285 2007 261 242 277 268 277 264 268 270 254 268 260 269

50

Alabama Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1991 1,825 1,776 1,759 1,668 1,765 1,492 1,869 1,541 2,011 857 1,610 1,972 1992 2,247 1,940 1,988 2,248 2,249 2,233 2,381 2,259 2,222 2,290 2,277 2,387 1993 2,340 1,872 2,111 1,945 1,407 1,747 2,269 2,331 2,270 2,338 2,232 2,457 1994 2,473 2,025 2,223 2,147 1,562 1,554 2,551 2,616 2,287 2,375 2,593 2,575 1995 2,412 2,008 2,181 2,136 1,597 1,475 2,496 2,591 2,213 2,314 2,581 2,576 1996 2,211 2,030 2,287 2,270 2,346 2,216 2,232 2,297 2,257 2,293 2,292 2,275 1997 2,336 2,076 2,333 2,284 2,206 1,787 2,210 2,225 2,387 2,564 2,349 2,447 1998 2,281 2,028 2,282 2,245 2,151 1,732 2,162 2,156 2,342 2,519 2,310 2,404

51

Louisiana Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 - - - - - - - - - - - - 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0 2009 0 0 0 0 0 0 0 0 0 0 0 0 2010 0 0 0 0 0 0 0 0 0 0 0 0 2011 NA NA NA NA NA NA NA NA NA NA NA NA 2012 NA NA NA NA NA NA NA NA NA NA NA NA

52

North Dakota Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 18 12 17 15 21 64 67 60 36 32 9 8 1997 6 6 8 6 5 5 10 24 47 13 28 5 1998 5 4 5 3 5 5 5 5 5 6 5 5 1999 5 6 7 7 7 8 6 8 6 6 5 5 2000 5 5 5 5 5 5 5 5 8 8 8 9 2001 9 7 7 6 7 6 9 8 8 8 7 7 2002 9 10 15 14 12 13 14 13 9 10 10 10 2003 11 10 10 10 11 11 11 12 9 10 9 9 2004 10 10 12 12 18 13 14 11 7 8 5 6 2005 6 6 7 6 7 8 9 8 8 8 7 7 2006 8 5 5 5 3 4 4 4 5 4 3 3 2007 6 4 4 4 2 3 3 3 4 3 2 2 2008 567 495 642 623 697 761 801 818 853 935 931 920 2009 614 540 589 564 544 513 535 536 497 479 483 349 2010 431 467 513 478 560 682 626 760 660 733 777 761

53

Montana Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

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

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 - - - - - - - - - - - - 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 134 102 102 102 24 20 27 7 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0 2009 0 0 0 0 0 0 0 0 0 0 0 0 2010 0 0 0 0 0 0 0 0 0 0 0 0 2011 NA NA NA NA NA NA NA NA NA NA NA NA 2012 NA NA NA NA NA NA NA NA NA NA NA NA

54

Missouri Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

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

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1991 0 0 0 0 0 0 0 0 0 0 0 0 1992 0 0 0 0 0 0 0 0 0 0 0 0 1993 0 0 0 0 0 0 0 0 0 0 0 0 1994 0 0 0 0 0 0 0 0 0 0 0 0 1995 0 0 0 0 0 0 0 0 0 0 0 0 1996 0 0 0 0 0 0 0 0 0 0 0 0 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2011 NA NA NA NA NA NA NA NA NA NA NA NA 2012 NA NA NA NA NA NA NA NA NA NA NA NA

55

Wyoming Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

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

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1991 2,374 2,117 2,567 2,440 2,313 2,308 2,342 2,478 2,317 2,472 2,521 2,381 1992 2,015 1,452 1,893 1,823 1,717 1,841 2,042 2,024 1,919 2,008 2,039 2,020 1993 13,055 11,433 13,119 12,645 13,201 6,119 12,956 13,525 13,301 13,884 14,076 13,925 1994 12,654 11,498 12,761 12,155 10,841 6,002 12,042 12,022 11,700 12,648 11,857 11,877 1995 13,054 11,340 12,181 12,297 12,586 12,154 12,287 10,493 12,228 12,613 12,100 12,391 1996 12,895 12,028 13,010 12,512 12,728 5,106 12,415 12,604 12,006 13,039 12,740 13,111 1997 13,025 11,329 13,134 12,620 12,437 9,809 12,318 12,317 11,967 12,304 12,546 12,607 1998 12,808 11,567 12,745 12,011 8,083 11,668 11,325 12,323 12,368 13,077 12,714 12,051

56

Utah Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 - - - - - - - - - - - - 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 730 790 769 1,205 963 766 715 704 861 583 478 765 2001 852 765 1,053 957 1,104 1,086 1,925 1,935 1,418 1,469 1,570 951 2002 1,221 1,265 1,334 1,269 1,197 1,224 1,354 1,285 1,259 1,525 1,172 1,115 2003 1,184 1,146 1,278 1,218 1,081 1,186 1,205 1,134 1,181 1,070 1,091 1,036 2004 991 932 942 895 880 864 744 961 883 886 823 790 2005 941 861 805 815 809 731 782 764 626 627 589 533 2006 695 479 534 493 469 447 463 485 497 555 530 469 2007 500 409 462 478 548 538 563 565 563 635 540 404

57

Maryland Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1991 0 0 0 0 0 0 0 0 0 0 0 0 1992 0 0 0 0 0 0 0 0 0 0 0 0 1993 0 0 0 0 0 0 0 0 0 0 0 0 1994 0 0 0 0 0 0 0 0 0 0 0 0 1995 0 0 0 0 0 0 0 0 0 0 0 0 1996 0 0 0 0 0 0 0 0 0 0 0 0 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0

58

Arizona Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

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

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 - - - - - - - - - - - - 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0 2009 0 0 0 0 0 0 0 0 0 0 0 0 2010 0 0 0 0 0 0 0 0 0 0 0 0 2011 NA NA NA NA NA NA NA NA NA NA NA NA 2012 NA NA NA NA NA NA NA NA NA NA NA NA

59

Utah Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

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

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 - - - - - - - - - - - - 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 730 790 769 1,205 963 766 715 704 861 583 478 765 2001 852 765 1,053 957 1,104 1,086 1,925 1,935 1,418 1,469 1,570 951 2002 1,221 1,265 1,334 1,269 1,197 1,224 1,354 1,285 1,259 1,525 1,172 1,115 2003 1,184 1,146 1,278 1,218 1,081 1,186 1,205 1,134 1,181 1,070 1,091 1,036 2004 991 932 942 895 880 864 744 961 883 886 823 790 2005 941 861 805 815 809 731 782 764 626 627 589 533 2006 695 479 534 493 469 447 463 485 497 555 530 469 2007 500 409 462 478 548 538 563 565 563 635 540 404

60

Texas Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

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

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1991 13,942 13,557 14,940 12,971 14,588 14,028 14,816 14,906 15,187 15,171 14,489 14,803 1992 15,418 14,446 14,043 15,744 15,716 14,929 15,203 15,313 14,243 15,567 14,513 14,868 1993 15,307 13,813 15,250 14,590 15,480 14,914 15,983 16,468 14,486 15,673 15,868 16,426 1994 16,557 15,133 16,303 16,449 16,781 16,234 14,410 15,490 16,853 17,348 17,080 17,827 1995 16,874 15,423 16,615 16,765 17,103 16,545 14,686 15,787 17,177 17,681 17,408 18,169 1996 18,965 18,527 19,905 18,331 17,193 19,390 18,370 21,654 21,126 20,005 23,391 22,041 1997 21,201 19,430 21,726 19,323 22,294 21,770 23,348 23,536 21,611 22,478 23,411 23,268

Note: This page contains sample records for the topic "gases removed increased" 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

California Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 71 76 80 78 78 76 80 79 77 79 78 80 1997 20 18 20 20 20 20 20 20 20 20 20 20 1998 62 56 62 60 62 60 62 62 60 62 60 62 1999 18 16 18 17 18 17 18 18 17 18 17 18 2000 22 20 22 22 22 22 22 22 22 22 22 22 2001 21 19 21 20 21 20 21 21 20 21 20 21 2002 224 203 227 211 219 217 217 410 274 304 330 299 2003 309 277 304 289 307 293 298 285 279 281 276 281 2004 284 260 273 270 278 269 278 275 270 279 272 277 2005 104 250 276 272 280 267 282 289 280 288 281 283 2006 277 256 293 283 293 280 283 286 269 284 275 285 2007 261 242 277 268 277 264 268 270 254 268 260 269

62

Wyoming Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1991 2,374 2,117 2,567 2,440 2,313 2,308 2,342 2,478 2,317 2,472 2,521 2,381 1992 2,015 1,452 1,893 1,823 1,717 1,841 2,042 2,024 1,919 2,008 2,039 2,020 1993 13,055 11,433 13,119 12,645 13,201 6,119 12,956 13,525 13,301 13,884 14,076 13,925 1994 12,654 11,498 12,761 12,155 10,841 6,002 12,042 12,022 11,700 12,648 11,857 11,877 1995 13,054 11,340 12,181 12,297 12,586 12,154 12,287 10,493 12,228 12,613 12,100 12,391 1996 12,895 12,028 13,010 12,512 12,728 5,106 12,415 12,604 12,006 13,039 12,740 13,111 1997 13,025 11,329 13,134 12,620 12,437 9,809 12,318 12,317 11,967 12,304 12,546 12,607 1998 12,808 11,567 12,745 12,011 8,083 11,668 11,325 12,323 12,368 13,077 12,714 12,051

63

Alaska Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 - - - - - - - - - - - - 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0 2009 0 0 0 0 0 0 0 0 0 0 0 0 2010 0 0 0 0 0 0 0 0 0 0 0 0 2011 0 0 0 0 0 0 0 0 0 0 0 0 2012 0 0 0 0 0 0 0 0 0 0 0 0 2013 NA NA NA NA NA NA NA NA NA NA

64

New Mexico Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 8,529 7,949 8,687 8,339 8,740 8,289 7,875 7,987 7,677 7,773 7,824 8,089 1997 12,133 12,133 12,133 12,133 12,133 12,133 12,133 12,133 12,133 12,133 12,133 12,133 1998 11,177 11,177 11,177 11,177 11,177 11,177 11,177 11,177 11,177 11,177 11,177 11,177 1999 12,787 11,548 12,722 12,443 12,412 12,599 12,654 12,926 12,327 12,927 12,633 11,671 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 2,219 1,984 2,391 2,117 2,392 2,251 2,373 2,639 2,554 2,728 2,619 2,696

65

Kentucky Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1991 0 0 0 0 0 0 0 0 0 0 0 0 1992 0 0 0 0 0 0 0 0 0 0 0 0 1993 0 0 0 0 0 0 0 0 0 0 0 0 1994 0 0 0 0 0 0 0 0 0 0 0 0 1995 0 0 0 0 0 0 0 0 0 0 0 0 1996 0 0 0 0 0 0 0 0 0 0 0 0 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0

66

Montana Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 - - - - - - - - - - - - 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 134 102 102 102 24 20 27 7 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0 2009 0 0 0 0 0 0 0 0 0 0 0 0 2010 0 0 0 0 0 0 0 0 0 0 0 0 2011 NA NA NA NA NA NA NA NA NA NA NA NA 2012 NA NA NA NA NA NA NA NA NA NA NA NA

67

Mississippi Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic  

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

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1991 4,713 4,103 4,177 3,429 3,291 3,200 3,548 3,901 3,708 4,067 3,907 3,971 1992 3,944 3,653 3,861 3,656 3,806 4,011 4,105 4,107 2,254 4,223 4,138 4,015 1993 4,031 3,622 3,992 3,857 4,043 4,213 4,447 4,201 4,173 4,150 3,845 3,441 1994 3,468 3,196 3,665 3,492 3,683 3,619 3,903 3,999 3,578 4,030 3,792 3,920 1995 810 747 857 816 861 846 912 935 836 942 886 916 1996 829 744 786 751 808 750 776 725 326 427 693 701 1997 718 631 684 659 641 598 633 677 752 775 723 676 1998 734 676 691 696 727 713 720 746 685 716 705 711 1999 697 637 667 553 559 532 537 516 490 525 498 493 2000 487 1,362 1,346 1,380 1,545 1,453 1,616 1,565 1,526 1,608 1,546 1,558

68

Louisiana Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic  

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

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 - - - - - - - - - - - - 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0 2009 0 0 0 0 0 0 0 0 0 0 0 0 2010 0 0 0 0 0 0 0 0 0 0 0 0 2011 NA NA NA NA NA NA NA NA NA NA NA NA 2012 NA NA NA NA NA NA NA NA NA NA NA NA

69

Oklahoma Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 - - - - - - - - - - - - 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0 2009 0 0 0 0 0 0 0 0 0 0 0 0 2010 0 0 0 0 0 0 0 0 0 0 0 0 2011 NA NA NA NA NA NA NA NA NA NA NA NA 2012 NA NA NA NA NA NA NA NA NA NA NA NA

70

Kansas Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 - - - - - - - - - - - - 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0 2009 0 0 0 0 0 0 0 0 0 0 0 0 2010 0 0 0 0 0 0 0 0 0 0 0 0 2011 NA NA NA NA NA NA NA NA NA NA NA NA 2012 NA NA NA NA NA NA NA NA NA NA NA NA

71

Florida Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 51 49 45 45 48 50 81 65 68 63 66 69 1997 69 66 79 72 70 58 67 65 67 59 57 64 1998 62 56 60 62 66 55 65 69 58 61 69 67 1999 67 58 64 59 55 51 65 74 68 68 73 65 2000 64 62 73 64 69 61 68 68 68 66 58 66 2001 59 51 56 64 57 61 71 68 63 90 49 46 2002 44 33 50 38 38 37 34 31 32 31 27 35 2003 30 26 30 27 27 36 35 30 35 38 34 37 2004 37 25 35 36 34 36 42 35 13 33 37 40 2005 43 31 37 33 36 27 12 19 26 26 25 23 2006 21 20 24 23 24 26 30 29 29 39 24 16 2007 15 15 17 17 17 19 22 21 21 29 17 12 2008 21 20 24 23 24 26 30 29 29 40 24 16 2009 2 2 3 2 3 3 3 3 3 4 3 2

72

Oregon Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 35 22 31 35 20 19 20 16 19 19 16 14 1997 15 14 14 14 14 14 14 14 12 14 13 14 1998 13 11 14 13 13 13 13 13 13 12 12 12 1999 12 12 20 19 19 19 18 13 15 21 22 23 2000 20 17 17 16 17 15 15 16 16 18 16 15 2001 1 1 1 1 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0 2009 0 0 0 0 0 0 0 0 0 0 0 0 2010 0 0 0 0 0 0 0 0 0 0 0 0 2011 0 0 0 0 0 0 0 0 0 0 0 0

73

Nevada Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1991 0 0 0 0 0 0 0 0 0 0 0 0 1992 0 0 0 0 0 0 0 0 0 0 0 0 1993 0 0 0 0 0 0 0 0 0 0 0 0 1994 0 0 0 0 0 0 0 0 0 0 0 0 1995 0 0 0 0 0 0 0 0 0 0 0 0 1996 0 0 0 0 0 0 0 0 0 0 0 0 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0

74

North Dakota Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic  

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

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 18 12 17 15 21 64 67 60 36 32 9 8 1997 6 6 8 6 5 5 10 24 47 13 28 5 1998 5 4 5 3 5 5 5 5 5 6 5 5 1999 5 6 7 7 7 8 6 8 6 6 5 5 2000 5 5 5 5 5 5 5 5 8 8 8 9 2001 9 7 7 6 7 6 9 8 8 8 7 7 2002 9 10 15 14 12 13 14 13 9 10 10 10 2003 11 10 10 10 11 11 11 12 9 10 9 9 2004 10 10 12 12 18 13 14 11 7 8 5 6 2005 6 6 7 6 7 8 9 8 8 8 7 7 2006 8 5 5 5 3 4 4 4 5 4 3 3 2007 6 4 4 4 2 3 3 3 4 3 2 2 2008 567 495 642 623 697 761 801 818 853 935 931 920 2009 614 540 589 564 544 513 535 536 497 479 483 349 2010 431 467 513 478 560 682 626 760 660 733 777 761

75

Michigan Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

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

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 - - - - - - - - - - - - 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0 2009 0 0 0 0 0 0 0 0 0 0 0 0 2010 0 0 0 0 0 0 0 0 0 0 0 0 2011 NA NA NA NA NA NA NA NA NA NA NA NA 2012 NA NA NA NA NA NA NA NA NA NA NA NA

76

Arkansas Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1991 0 0 0 0 0 0 0 0 0 0 0 0 1992 0 0 0 0 0 0 0 0 0 0 0 0 1993 0 0 0 0 0 0 0 0 0 0 0 0 1994 0 0 0 0 0 0 0 0 0 0 0 0 1995 0 0 0 0 0 0 0 0 0 0 0 0 1996 0 0 0 0 0 0 0 0 0 0 0 0 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0

77

Michigan Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 - - - - - - - - - - - - 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0 2009 0 0 0 0 0 0 0 0 0 0 0 0 2010 0 0 0 0 0 0 0 0 0 0 0 0 2011 0 0 0 0 0 0 0 0 0 0 0 0 2012 0 0 0 0 0 0 0 0 0 0 0 0 2013 NA NA NA NA NA NA NA NA NA NA

78

West Virginia Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1991 0 0 0 0 0 0 0 0 0 0 0 0 1992 0 0 0 0 0 0 0 0 0 0 0 0 1993 0 0 0 0 0 0 0 0 0 0 0 0 1994 0 0 0 0 0 0 0 0 0 0 0 0 1995 0 0 0 0 0 0 0 0 0 0 0 0 1996 0 0 0 0 0 0 0 0 0 0 0 0 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0

79

Nebraska Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1991 0 0 0 0 0 0 0 0 0 0 0 0 1992 0 0 0 0 0 0 0 0 0 0 0 0 1993 0 0 0 0 0 0 0 0 0 0 0 0 1994 0 0 0 0 0 0 0 0 0 0 0 0 1995 0 0 0 0 0 0 0 0 0 0 0 0 1996 0 0 0 0 0 0 0 0 0 0 0 0 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0

80

Arizona Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

Gasoline and Diesel Fuel Update (EIA)

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 - - - - - - - - - - - - 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0 2009 0 0 0 0 0 0 0 0 0 0 0 0 2010 0 0 0 0 0 0 0 0 0 0 0 0 2011 0 0 0 0 0 0 0 0 0 0 0 0 2012 0 0 0 0 0 0 0 0 0 0 0 0 2013 NA NA NA NA NA NA NA NA NA NA

Note: This page contains sample records for the topic "gases removed increased" from the National Library of EnergyBeta (NLEBeta).
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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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81

Oklahoma Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

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

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 - - - - - - - - - - - - 1997 0 0 0 0 0 0 0 0 0 0 0 0 1998 0 0 0 0 0 0 0 0 0 0 0 0 1999 0 0 0 0 0 0 0 0 0 0 0 0 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 0 0 0 0 0 0 0 0 0 0 0 0 2008 0 0 0 0 0 0 0 0 0 0 0 0 2009 0 0 0 0 0 0 0 0 0 0 0 0 2010 0 0 0 0 0 0 0 0 0 0 0 0 2011 NA NA NA NA NA NA NA NA NA NA NA NA 2012 NA NA NA NA NA NA NA NA NA NA NA NA

82

New Mexico Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic  

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

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1996 8,529 7,949 8,687 8,339 8,740 8,289 7,875 7,987 7,677 7,773 7,824 8,089 1997 12,133 12,133 12,133 12,133 12,133 12,133 12,133 12,133 12,133 12,133 12,133 12,133 1998 11,177 11,177 11,177 11,177 11,177 11,177 11,177 11,177 11,177 11,177 11,177 11,177 1999 12,787 11,548 12,722 12,443 12,412 12,599 12,654 12,926 12,327 12,927 12,633 11,671 2000 0 0 0 0 0 0 0 0 0 0 0 0 2001 0 0 0 0 0 0 0 0 0 0 0 0 2002 0 0 0 0 0 0 0 0 0 0 0 0 2003 0 0 0 0 0 0 0 0 0 0 0 0 2004 0 0 0 0 0 0 0 0 0 0 0 0 2005 0 0 0 0 0 0 0 0 0 0 0 0 2006 0 0 0 0 0 0 0 0 0 0 0 0 2007 2,219 1,984 2,391 2,117 2,392 2,251 2,373 2,639 2,554 2,728 2,619 2,696

83

Alabama Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

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

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1991 1,825 1,776 1,759 1,668 1,765 1,492 1,869 1,541 2,011 857 1,610 1,972 1992 2,247 1,940 1,988 2,248 2,249 2,233 2,381 2,259 2,222 2,290 2,277 2,387 1993 2,340 1,872 2,111 1,945 1,407 1,747 2,269 2,331 2,270 2,338 2,232 2,457 1994 2,473 2,025 2,223 2,147 1,562 1,554 2,551 2,616 2,287 2,375 2,593 2,575 1995 2,412 2,008 2,181 2,136 1,597 1,475 2,496 2,591 2,213 2,314 2,581 2,576 1996 2,211 2,030 2,287 2,270 2,346 2,216 2,232 2,297 2,257 2,293 2,292 2,275 1997 2,336 2,076 2,333 2,284 2,206 1,787 2,210 2,225 2,387 2,564 2,349 2,447 1998 2,281 2,028 2,282 2,245 2,151 1,732 2,162 2,156 2,342 2,519 2,310 2,404

84

BIOSIGNATURE GASES IN H?-DOMINATED ATMOSPHERES ON ROCKY EXOPLANETS  

E-Print Network (OSTI)

Super-Earth exoplanets are being discovered with increasing frequency and some will be able to retain stable H2-dominated atmospheres. We study biosignature gases on exoplanets with thin H2 atmospheres and habitable surface ...

Seager, Sara

85

Control of pollutants in flue gases and fuel gases  

E-Print Network (OSTI)

and gasification technologies for heat and power . . . . . . . . 2-3 2.4 Waste incineration and waste . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-1 2.2 Flue gases and fuel gases: combustion, gasification, pyrolysis, incineration and other . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3 3.3 Formation of sulphur compounds during combustion and gasification . 3-5 3.4 Emission

Laughlin, Robert B.

86

Control of pollutants in flue gases and fuel gases  

E-Print Network (OSTI)

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-1 2.2 Flue gases and fuel gases: combustion, gasification, pyrolysis, incineration and other and gasification technologies for heat and power . . . . . . . . 2-3 2.4 Waste incineration and waste . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3 3.3 Formation of sulphur compounds during combustion and gasification . . 3-5 3.4 Emission

Zevenhoven, Ron

87

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

88

Molybdenum-based additives to mixed-metal oxides for use in hot gas cleanup sorbents for the catalytic decomposition of ammonia in coal gases  

DOE Patents (OSTI)

This invention relates to additives to mixed-metal oxides that act simultaneously as sorbents and catalysts in cleanup systems for hot coal gases. Such additives of this type, generally, act as a sorbent to remove sulfur from the coal gases while substantially simultaneously, catalytically decomposing appreciable amounts of ammonia from the coal gases.

Ayala, Raul E. (Clifton Park, NY)

1993-01-01T23:59:59.000Z

89

Federal Energy Management Program: Greenhouse Gases  

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

Greenhouse Gases Greenhouse Gases to someone by E-mail Share Federal Energy Management Program: Greenhouse Gases on Facebook Tweet about Federal Energy Management Program: Greenhouse Gases on Twitter Bookmark Federal Energy Management Program: Greenhouse Gases on Google Bookmark Federal Energy Management Program: Greenhouse Gases on Delicious Rank Federal Energy Management Program: Greenhouse Gases on Digg Find More places to share Federal Energy Management Program: Greenhouse Gases on AddThis.com... Sustainable Buildings & Campuses Operations & Maintenance Greenhouse Gases Basics Federal Requirements Guidance & Reporting Inventories & Performance Mitigation Planning Resources Contacts Water Efficiency Data Center Energy Efficiency Industrial Facilities Sustainable Federal Fleets

90

Voluntary Reporting of Greenhouse Gases  

Reports and Publications (EIA)

The Voluntary Reporting of Greenhouse Gases Program was suspended May 2011. It was a mechanism by which corporations, government agencies, individuals, voluntary organizations, etc., could report to the Energy Information Administration, any actions taken that have or are expected to reduce/avoid emissions of greenhouse gases or sequester carbon.

2011-01-01T23:59:59.000Z

91

Silica Scaling Removal Process  

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

Silica Scaling Removal Process Silica Scaling Removal Process Silica Scaling Removal Process Scientists at Los Alamos National Laboratory have developed a novel technology to remove both dissolved and colloidal silica using small gel particles. Available for thumbnail of Feynman Center (505) 665-9090 Email Silica Scaling Removal Process Applications: Cooling tower systems Water treatment systems Water evaporation systems Potential mining applications (produced water) Industry applications for which silica scaling must be prevented Benefits: Reduces scaling in cooling towers by up to 50% Increases the number of cycles of concentration substantially Reduces the amount of antiscaling chemical additives needed Decreases the amount of makeup water and subsequent discharged water (blowdown) Enables considerable cost savings derived from reductions in

92

Greenhouse Gases | Department of Energy  

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

Greenhouse Gases Greenhouse Gases Greenhouse Gases October 7, 2013 - 9:59am Addthis Executive Order 13514 requires Federal agencies to inventory and manage greenhouse gas (GHG) emissions to meet Federal goals and mitigate climate change. Basics: Read an overview of greenhouse gases. Federal Requirements: Look up requirements for agency greenhouse gas management as outlined in Federal initiatives and executive orders. Guidance and Reporting: Find guidance documents and resources for greenhouse gas accounting and reporting. GHG Inventories and Performance: See detailed comprehensive GHG inventories by Federal agency and progress toward achieving Scope 1 and 2 GHG and Scope 3 GHG reduction targets. Mitigation Planning: Learn how Federal agencies can cost-effectively meet their GHG reduction goals.

93

Degenerate quantum gases of strontium  

E-Print Network (OSTI)

Degenerate quantum gases of alkaline-earth-like elements open new opportunities in research areas ranging from molecular physics to the study of strongly correlated systems. These experiments exploit the rich electronic structure of these elements, which is markedly different from the one of other species for which quantum degeneracy has been attained. Specifically, alkaline-earth-like atoms, such as strontium, feature metastable triplet states, narrow intercombination lines, and a non-magnetic, closed-shell ground state. This review covers the creation of quantum degenerate gases of strontium and the first experiments performed with this new system. It focuses on laser-cooling and evaporation schemes, which enable the creation of Bose-Einstein condensates and degenerate Fermi gases of all strontium isotopes, and shows how they are used for the investigation of optical Feshbach resonances, the study of degenerate gases loaded into an optical lattice, as well as the coherent creation of Sr_2 molecules.

Stellmer, Simon; Killian, Thomas C

2013-01-01T23:59:59.000Z

94

Turning greenhouse gases into gold  

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

gases, with carbon dioxide (CO2) often accused of being the primary instigator of global climate change. As a result, numerous efforts are under way to find ways to prevent,...

95

ARM - What are Greenhouse Gases?  

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

radiative forcing (which means they enhance global warming). Many of these gases are naturally occurring and are essential to life on earth by providing a blanket for marine and...

96

Greenhouse Gases and Emissions Trading  

Science Journals Connector (OSTI)

Atmospheric concentrations of carbon dioxide and other greenhouse gases have grown rapidly since the beginning of this century. Unless emissions are controlled, the world could face rapid climate changes, incl...

Alice LeBlanc; Daniel J. Dudek

1993-01-01T23:59:59.000Z

97

Climate VISION: Greenhouse Gases Information  

Office of Scientific and Technical Information (OSTI)

GHG Information GHG Information Greenhouse Gases, Global Climate Change, and Energy Emissions of Greenhouse Gases in the United States 2001 [1605(a)] This report, required by Section 1605(a) of the Energy Policy Act of 1992, provides estimates of U.S. emissions of greenhouse gases, as well as information on the methods used to develop the estimates. The estimates are based on activity data and applied emissions factors, not on measured or metered emissions monitoring. Available Energy Footprints Industry NAICS* All Manufacturing Alumina & Aluminum 3313 Cement 327310 Chemicals 325 Fabricated Metals 332 Food and Beverages 311, 312 Forest Products 321, 322 Foundries 3315 Glass & Glass Products, Fiber Glass 3272, 3296 Iron & Steel Mills 331111 Machinery & Equipment 333, 334, 335, 336

98

Investigating and Using Biomass Gases  

K-12 Energy Lesson Plans and Activities Web site (EERE)

Students will be introduced to biomass gasification and will generate their own biomass gases. Students generate these everyday on their own and find it quite amusing, but this time theyll do it by heating wood pellets or wood splints in a test tube. They will collect the resulting gases and use the gas to roast a marshmallow. Students will also evaluate which biomass fuel is the best according to their own criteria or by examining the volume of gas produced by each type of fuel.

99

Clean Gases for Gas Chromatography  

Science Journals Connector (OSTI)

......to purchase such clean gases. Even research grades...no maintenance, at the cost of 500 watts of electrical...Exploration and Production Research Division, Hous...hour. The maintenance cost of the cold trap is only...displaces the contaminated gas which has passed into......

B. Osborne Prescott; Harold L. Wise

1966-02-01T23:59:59.000Z

100

Effects of catalysts and additives on fluorocarbon removal with surface discharge plasma  

Science Journals Connector (OSTI)

The decomposition of fluorocarbons (1%) in Ar was investigated using a surface discharge-type plasma reactor. To enhance the effectiveness of plasma chemical processing, we investigated the effects of catalysts and additives. The removal rate increased when the plasma reactor was packed with TiO2 pellets as a catalyst. The catalytic effect seems to be derived from the direct activation of the TiO2 surface by the plasma discharge, because significant UV emission and temperature increase were not observed in the plasma reactor. The removal rate was also enhanced when water vapor, oxygen, or hydrogen was added to the reactant. In addition, the presence of TiO2 or the additional gases or both depressed byproduct formation. Analysis of the reaction products suggested that the catalysts and additives enhanced the process by preventing the recombination of decomposed fragments.

Atsushi Ogata; Hyun-Ha Kim; Shigeru Futamura; Satoshi Kushiyama; Koichi Mizuno

2004-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "gases removed increased" 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

Industrial Gases as a Vehicle for Competitiveness  

E-Print Network (OSTI)

the diversity and options available to enable cost savings and environmentally driven process improvements. Industrial gases have come of age during the last fifteen years. Engineers and scientists have looked beyond the paradigms of their operations...INDUSTRIAL GASES AS A VEHICLE FOR COMPETITIVENESS James R. Dale, Director, Technology Programs, Airco Industrial Gases Division, The BOC Group, Inc., Murray Hill, New Jersey ABSTRACT Industrial gases are produced using compressed air...

Dale, J. R.

102

CO2 Separation from Low-Temperature Flue Gases  

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

partners interested in implementing United States Patent Number 7,842,126 entitled "Co 2 Separation from Low-Temperature Flue Gases." Disclosed in this patent are novel methods for processing carbon dioxide (CO 2 ) from combustion gas streams. Researchers at NETL are focused on the development of novel sorbent systems that can effectively remove CO 2 and other gases in an economically feasible manner with limited impact on energy production cost. The current invention will help in reducing greenhouse gas emissions by using an improved, regenerable aqueous amine and soluble potassium carbonate sorbent system. This novel solvent system may be capable of achieving CO 2 capture from larger emission streams at lower overall cost. Overview Sequestration of CO

103

Silica Scaling Removal Process  

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

Silica Scaling Removal Process Silica Scaling Removal Process Scientists at Los Alamos National Laboratory have developed a novel technology to remove both dissolved and colloidal...

104

Greenhouse Gases Converted to Fuel  

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

Greenhouse Greenhouse Gases Converted to Fuel Greenhouse Gases Converted to Fuel carbon-conversion-fig-1.jpg Key Challenges: An important strategy for reducing global CO2 emissions calls for capturing the greenhouse gas and converting it to fuels and chemicals. Although researchers working toward that goal demonstrated in 1992 such a reaction in the lab, a key outstanding scientific challenge was explaining the details of how the reaction took place - its "mechanism." Why it Matters: An important potential strategy for reducing global CO2 emissions calls for capturing the greenhouse gas and converting it electrochemically to fuels and chemicals. Accomplishments: Computation to explain how carbon dioxide can be converted to small organic molecules with little energy input. The

105

Methods and compositions for removing carbon dioxide from a gaseous mixture  

DOE Patents (OSTI)

Provided is a method for adsorbing or separating carbon dioxide from a mixture of gases by passing the gas mixture through a porous three-dimensional polymeric coordination compound having a plurality of layers of two-dimensional arrays of repeating structural units, which results in a lower carbon dioxide content in the gas mixture. Thus, this invention provides useful compositions and methods for removal of greenhouse gases, in particular CO.sub.2, from industrial flue gases or from the atmosphere.

Li, Jing; Wu, Haohan

2014-06-24T23:59:59.000Z

106

Use of low temperature blowers for recirculation of hot gases  

DOE Patents (OSTI)

An apparatus is described for maintaining motors at low operating temperatures during recirculation of hot gases in fuel cell operations and chemical processes such as fluidized bed coal gasification. The apparatus includes a means for separating the hot process gas from the motor using a secondary lower temperature gas, thereby minimizing the temperature increase of the motor and associated accessories.

Maru, H.C.; Forooque, M.

1982-08-19T23:59:59.000Z

107

THE GREENHOUSE EFFECT RISING GREENHOUSE GASES AND CLIMATE CHANGE  

E-Print Network (OSTI)

, methane, and nitrous oxides. The sun's energy passes through these gases, like light passing through risen by almost 40 percent. This is attributed primarily to the burning of fossil fuels (coal, oil, gasoline). Methane and nitrous oxides are also increasing rapidly, due in part to the expansion

108

Carbonaceous adsorbent regeneration and halocarbon displacement by hydrocarbon gases  

DOE Patents (OSTI)

This invention describes a process for regeneration of halocarbon bearing carbonaceous adsorbents through which a carbonaceous adsorbent is contacted with hydrocarbon gases, preferably propane, butane and pentane at near room temperatures and at atmospheric pressure. As the hydrocarbon gases come in contact with the adsorbent, the hydrocarbons displace the halocarbons by physical adsorption. As a result of using this process, the halocarbon concentration and the hydrocarbon eluant is increased thereby allowing for an easier recovery of pure halocarbons. By using the process of this invention, carbonaceous adsorbents can be regenerated by an inexpensive process which also allows for subsequent re-use of the recovered halocarbons. 8 figures.

Senum, G.I.; Dietz, R.N.

1994-04-05T23:59:59.000Z

109

Carbonaceous adsorbent regeneration and halocarbon displacement by hydrocarbon gases  

DOE Patents (OSTI)

This invention describes a process for regeneration of halocarbon bearing carbonaceous adsorbents through which a carbonaceous adsorbent is contacted with hydrocarbon gases, preferably propane, butane and pentane at near room temperatures and at atmospheric pressure. As the hydrocarbon gases come in contact with the adsorbent, the hydrocarbons displace the halocarbons by physical adsorption. As a result of using this process, the halocarbon concentration and the hydrocarbon eluant is increased thereby allowing for an easier recovery of pure halocarbons. By using the process of this invention, carbonaceous adsorbents can be regenerated by an inexpensive process which also allows for subsequent re-use of the recovered halocarbons.

Senum, Gunnar I. (Patchogue, NY); Dietz, Russell N. (Patchogue, NY)

1994-01-01T23:59:59.000Z

110

Asia-wide emissions of greenhouse gases  

SciTech Connect

Emissions of principal greenhouse gases (GHGs) from Asia are increasing faster than those from any other continent. This is a result of rapid economic growth, as well as the fact that almost half of the world`s population lives in Asian countries. In this paper, the author provides estimates of emissions of the two principal greenhouse gases, carbon dioxide (CO{sub 2}) and methane (CH{sub 4}), from individual countries and areas. Recent literature has been reviewed for emission estimates for individual sources, such as carbon dioxide from cement manufacture, and methane from rice fields. There are very large uncertainties in many of these estimates, so several estimates are provided, where available. The largest anthropogenic source of CO{sub 2} emissions is the use of fossil fuels. Energy consumption data from 1992 have been used to calculate estimated emissions of CO{sub 2} from this source. In view of the ongoing negotiations to limit future greenhouse gas emissions, estimates of projected CO{sub 2} emissions from the developing countries of Asia are also provided. These are likely to be 3 times their 1986 levels by 2010, under business as usual scenarios. Even with the implementation of energy efficiency measures and fuel switching where feasible, the emissions of CO{sub 2} are likely to double within the same time period.

Siddiqi, T.A. [East-West Center, Honolulu, HI (United States). Program on Environment

1995-11-01T23:59:59.000Z

111

The Viscosity of Compressed Gases  

Science Journals Connector (OSTI)

New data and a new theory for the viscosity of compressed gases are presented. Data for nitrogen, hydrogen and a mixture of these gases are given, in the calculation of which, the "end effects" are not neglected as has been done in the past. Previous viscosity data are of doubtful validity owing to neglect of this factor. The theory is based on an analogy between the kinetic pressure and viscosity of a gas and is derived using an equation of state of the Lorentz type. Allowance is made for the difference between the viscosity and compressibility covolumes. The theory is substantiated experimentally and further confirmed by the recalculation of other data on the variation of Reynolds' criterion with the pressure, which is here shown to be constant. The mixture data offer a direct opportunity of comparing the Lorentz and linear rules for the calculation of the covolume of a mixture from the covolumes of the components and such comparison indicates that the Lorentz rule is not to be preferred. The substantiation of the new theory is the first direct proof of the validity of the separate treatment of the kinetic and cohesive pressures in the equation of state.

James H. Boyd; Jr.

1930-05-15T23:59:59.000Z

112

ARM - Lesson Plans: Dissolved Gases in Water  

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

released into the air, additional CO2 Would intensify an already-problematic greenhouse effect. Preparation Demonstrate that water contains invisible gases. Collect and cover...

113

Granular gases under extreme driving  

E-Print Network (OSTI)

We study inelastic gases in two dimensions using event-driven molecular dynamics simulations. Our focus is the nature of the stationary state attained by rare injection of large amounts of energy to balance the dissipation due to collisions. We find that under such extreme driving, with the injection rate much smaller than the collision rate, the velocity distribution has a power-law high energy tail. The numerically measured exponent characterizing this tail is in excellent agreement with predictions of kinetic theory over a wide range of system parameters. We conclude that driving by rare but powerful energy injection leads to a well-mixed gas and constitutes an alternative mechanism for agitating granular matter. In this distinct nonequilibrium steady-state, energy cascades from large to small scales. Our simulations also show that when the injection rate is comparable with the collision rate, the velocity distribution has a stretched exponential tail.

W. Kang; J. Machta; E. Ben-Naim

2010-02-04T23:59:59.000Z

114

Raman Spectra of Polyatomic Gases  

Science Journals Connector (OSTI)

Raman spectra of gaseous CO2, N2O, NH3, CH4 and C2H4 have been photographed using the line ?2536 of mercury as the exciting radiation. Vibrational transitions have been observed in all the gases investigated, and rotational transitions in the cases of NH3 and CH4. For the frequency shifts due to the vibrational transitions, the following numerical values (in cm-1) have been found: CO2: 1264.5; 1285.1; 1387.7; 1408.4.CH4: 2914.8; 3022.1; 3071.5.N2O: 1281.8C2H4: 1342.4; 1623.3; 2880.1; 3019.3; 3240.3; 3272.3.NH3: 3333.6 Raman spectra of liquid NH3 have been photographed and found to give the two frequency shifts: 3298.4 and 3214.5. In the case of gaseous NH3, pure rotational transitions lead to a moment of inertia having the value I0=2.7910-40. In the case of methane, the positive and negative branches of the 3022.1 band lead to the value I0=5.1710-40. The relations between these data and infra-red absorption data are discussed.

R. G. Dickinson, R. T. Dillon, and F. Rasetti

1929-08-15T23:59:59.000Z

115

Mercury and tritium removal from DOE waste oils  

SciTech Connect

This work covers the investigation of vacuum extraction as a means to remove tritiated contamination as well as the removal via sorption of dissolved mercury from contaminated oils. The radiation damage in oils from tritium causes production of hydrogen, methane, and low-molecular-weight hydrocarbons. When tritium gas is present in the oil, the tritium atom is incorporated into the formed hydrocarbons. The transformer industry measures gas content/composition of transformer oils as a diagnostic tool for the transformers` condition. The analytical approach (ASTM D3612-90) used for these measurements is vacuum extraction of all gases (H{sub 2}, N{sub 2}, O{sub 2}, CO, CO{sub 2}, etc.) followed by analysis of the evolved gas mixture. This extraction method will be adapted to remove dissolved gases (including tritium) from the SRS vacuum pump oil. It may be necessary to heat (60{degrees}C to 70{degrees}C) the oil during vacuum extraction to remove tritiated water. A method described in the procedures is a stripper column extraction, in which a carrier gas (argon) is used to remove dissolved gases from oil that is dispersed on high surface area beads. This method appears promising for scale-up as a treatment process, and a modified process is also being used as a dewatering technique by SD Myers, Inc. (a transformer consulting company) for transformers in the field by a mobile unit. Although some mercury may be removed during the vacuum extraction, the most common technique for removing mercury from oil is by using sulfur-impregnated activated carbon (SIAC). SIAC is currently being used by the petroleum industry to remove mercury from hydrocarbon mixtures, but the sorbent has not been previously tested on DOE vacuum oil waste. It is anticipated that a final process will be similar to technologies used by the petroleum industry and is comparable to ion exchange operations in large column-type reactors.

Klasson, E.T. [Oak Ridge National Lab., TN (United States)

1997-10-01T23:59:59.000Z

116

Comparing greenhouse gases for policy purposes  

E-Print Network (OSTI)

In order to derive optimal policies for greenhouse gas emissions control, the discounted marginal damages of emissions of different gases must be compared. The greenhouse warming potential (GWP) index, which is most often ...

Schmalensee, Richard

1993-01-01T23:59:59.000Z

117

Voluntary reporting of greenhouse gases, 1995  

SciTech Connect

The Voluntary Reporting Program for greenhouse gases is part of an attempt by the U.S. Government to develop innovative, low-cost, and nonregulatory approaches to limit emissions of greenhouse gases. It is one element in an array of such programs introduced in recent years as part of the effort being made by the United States to comply with its national commitment to stabilize emissions of greenhouse gases under the Framework Convention on Climate Change. The Voluntary Reporting Program, developed pursuant to Section 1605(b) of the Energy Policy Act of 1992, permits corporations, government agencies, households, and voluntary organizations to report to the Energy Information Administration (EIA) on actions taken that have reduced or avoided emissions of greenhouse gases.

NONE

1996-07-01T23:59:59.000Z

118

Gases for an SSC muon detector  

SciTech Connect

Recent measurements of electron drift velocities as a function of the density-reduced electric field E/N are reported for a number of unitary gases and the mixtures CO{sub 2}/CH{sub 4} and NH{sub 3}/CF{sub 4}/Ar. Calculated values of the mean electron energy as a function of E/N are also reported for unitary gases and mixtures of CO{sub 2}/CH{sub 4}. 7 refs., 5 figs.

Christophorou, L.G.; Datskos, P.G.; Carter, J.G. (Oak Ridge National Lab., TN (USA) Tennessee Univ., Knoxville, TN (USA). Dept. of Physics and Astronomy)

1990-01-01T23:59:59.000Z

119

Removal of ash from Indian Assam coking coal using sodium hydroxide and acid solutions  

SciTech Connect

Mineral matter (ash) removal from Assam coking coal by leaching with different concentrations of sodium hydroxide and acid (HCl, H{sub 2}SO{sub 4}, HNO{sub 3}, and HF) solutions has been investigated at a temperature of 75 C. The parameters tested were concentration of NaOH, type of acid, concentration of acids, and number of acid leaching steps. Total ash removed increased with increase of NaOH and acid concentrations up to the range studied. For the same experimental conditions, treatment of caustic leached coal in HCl acid resulted in better demineralization than in H{sub 2}SO{sub 4} or HNO{sub 3} acid. In the NaOH-HNO{sub 3} leaching method, a higher concentration (>20%) of HNO{sub 3} acid had an adverse effect on the de-ashing of coal. The NaOH-HF leaching process has been found to be the most effective method of coal de-ashing. The two acid treatment steps (HCl-H{sub 2}SO{sub 4}/HCl-HNO{sub 3}) after caustic leaching are the next most effective methods of coal de-ashing. The removal of mineral matter (including S) from coal is expected to decrease the graphite reactivity and thus the atmospheric pollution (due to the generation of smaller quantities of CO and SO{sub 2} gases).

Kumar, M.; Shankar, R.H.

2000-03-01T23:59:59.000Z

120

Purification of Natural Gases with High CO2 Content Using Gas Hydrates  

Science Journals Connector (OSTI)

Purification of Natural Gases with High CO2 Content Using Gas Hydrates ... The feed was separated using a cascade of continuously stirred tank crystallizer vessels, which can also be regarded as an ideal crystallizer column resembling a gas-hydrate-based scrubbing process. ... Pressurized gas scrubbing, pressure swing adsorption, chemical absorption, and membrane and cryogenic processes are some examples of well-established technologies for the removal of CO2 from gaseous products. ...

Nena Dabrowski; Christoph Windmeier; Lothar R. Oellrich

2009-09-25T23:59:59.000Z

Note: This page contains sample records for the topic "gases removed increased" 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

Turbomachinery debris remover  

DOE Patents (OSTI)

An apparatus for removing debris from a turbomachine. The apparatus includes housing and remotely operable viewing and grappling mechanisms for the purpose of locating and removing debris lodged between adjacent blades in a turbomachine.

Krawiec, Donald F. (Pittsburgh, PA); Kraf, Robert J. (North Huntingdon, PA); Houser, Robert J. (Monroeville, PA)

1988-01-01T23:59:59.000Z

122

THE FUTURE OF ENERGY GASES David G. Howell, Editor  

E-Print Network (OSTI)

totally independent of oil. Methane is found in association with coal; it is a byproduct of metabolic the term "energy gases" to distinguish those natural gases, primarily methane, that have utility for energy consequences associated with an expanded role of energy gases? Energy gases, particularly methane, are commonly

123

Measuring the Isotopic Composition of Solar Wind Noble Gases  

E-Print Network (OSTI)

noble gases. #12;Exploring the Solar Wind94 Light solar wind noble gases were directly measured by mass of the light gases are known to vary with energy, so none of these provided solar isotopic and elemental5 Measuring the Isotopic Composition of Solar Wind Noble Gases Alex Meshik, Charles Hohenberg, Olga

124

Production of quantum degenerate strontium gases: Larger, better, faster, colder  

E-Print Network (OSTI)

We report on an improved scheme to generate Bose-Einstein condensates (BECs) and degenerate Fermi gases of strontium. This scheme allows us to create quantum gases with higher atom number, a shorter time of the experimental cycle, or deeper quantum degeneracy than before. We create a BEC of 84-Sr exceeding 10^7 atoms, which is a 30-fold improvement over previously reported experiments. We increase the atom number of 86-Sr BECs to 2.5x10^4 (a fivefold improvement), and refine the generation of attractively interacting 88-Sr BECs. We present a scheme to generate 84-Sr BECs with a cycle time of 2s, which, to the best of our knowledge, is the shortest cycle time of BEC experiments ever reported. We create deeply-degenerate 87-Sr Fermi gases with T/T_F as low as 0.10(1), where the number of populated nuclear spin states can be set to any value between one and ten. Furthermore, we report on a total of five different double-degenerate Bose-Bose and Bose-Fermi mixtures. These studies prepare an excellent starting poi...

Stellmer, Simon; Schreck, Florian

2012-01-01T23:59:59.000Z

125

Purchase, Delivery, and Storage of Gases  

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

Purchase, Delivery, and Storage of Gases Print Purchase, Delivery, and Storage of Gases Print ALS users should follow Berkeley Lab policy, as described below, for the purchase, delivery, storage, and use of all gases at the ALS. See Shipping and Receiving for information on any non-gas deliveries. Contacts: Gas purchase or delivery: ALS Receiving, 510-486-4494 Gas use and storage: Experiment Coordination, 510-486-7222, This e-mail address is being protected from spambots. You need JavaScript enabled to view it Gas Storage: Berkeley Lab Chemical Inventory All gas bottles and cylinders at the ALS must be identified with bar code and logged into the Berkeley Lab Chemical Inventory by ALS staff. The inventory will be updated periodically; for more information contact Experiment Coordination. Gases are stored either in the racks between buildings 6 and 7; toxic and corrosive gases are stored in Building 6, room 6C across the walkway from beamline 10.0.

126

Sorption of organic gases in residential rooms  

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

residential rooms residential rooms Title Sorption of organic gases in residential rooms Publication Type Journal Article LBNL Report Number LBNL-59303 Year of Publication 2007 Authors Singer, Brett C., Alfred T. Hodgson, Toshifumi Hotchi, Katherine Y. Ming, Richard G. Sextro, Emily E. Wood, and Nancy J. Brown Journal Atmospheric Environment Volume 41 Start Page Chapter Pagination 3251-3265 Keywords adsorption, hazardous air pollutants, nerve agents, sink effect, volatile organic compounds Abstract Experiments were conducted to characterize organic gas sorption in residential rooms studied ''as-is'' with furnishings and material surfaces unaltered and in a furnished chamber designed to simulate a residential room. Results are presented for 10 rooms (five bedrooms, two bathrooms, a home office, and two multi-function spaces) and the chamber. Exposed materials were characterized and areas quantified. A mixture of volatile organic compounds (VOCs) was rapidly volatilized within each room as it was closed and sealed for a 5-h Adsorb phase; this was followed by 30-min Flush and 2-h closed-room Desorb phases. Included were alkane, aromatic, and oxygenated VOCs representing a range of ambient and indoor air pollutants. Three organophosphorus compounds served as surrogates for Sarin-like nerve agents. Measured gas-phase concentrations were fit to three variations of a mathematical model that considers sorption occurring at a surface sink and potentially a second, embedded sink. The 3-parameter sink-diffusion model provided acceptable fits for most compounds and the 4-parameter two-sink model provided acceptable fits for the others. Initial adsorption rates and sorptive partitioning increased with decreasing vapor pressure for the alkanes, aromatics and oxygenated VOCs. Best-fit sorption parameters obtained from experimental data from the chamber produced best-fit sorption parameters similar to those obtained from the residential rooms

127

Ion fragmentation in an electrospray ionization mass spectrometer interface with different gases  

E-Print Network (OSTI)

in the gas phase. However, particularly in multi- component samples, this may not be enough to unambigu predicts that the degree of ion fragmentation increases with increasing mass of the curtain gas. However with argon and krypton is caused by condensation of the gases within the free jet expansion between

Chen, David D.Y.

128

Emissions of greenhouse gases in the United States, 1985--1990  

SciTech Connect

The Earth`s capacity to support life depends on the moderating influences of gases that envelop the planet and warm its surface and protect it from harmful radiation. These gases are referred to as ``greenhouse gases.`` Their warming capacity, called ``the greenhouse effect,`` is essential to maintaining a climate hospitable to all plant, animal, and human life. In recent years, however, there has been increasing concern that human activity may be affecting the intricate balance between the Earth`s absorption of heat from the sun and its capacity to reradiate excess heat back into space. Emissions of greenhouse gases from human activities may be an important mechanism that affects global climate. Thus, research is intensifying to improve our understanding of the role human activities might play in influencing atmospheric concentrations of greenhouse gases. On the basis of scientific findings of the past few decades, the US Government and the international community at large are now taking steps toward stabilizing greenhouse gas emissions. This report contributes to that process. Mandated by Congress this report provides estimates of US emissions of the principal greenhouse gases--carbon dioxide, methane, nitrous oxide, chlorofluorcarbons, carbon monoxide, nitrogen oxides, and nonmethane volatile organic compounds. Estimates are for the period 1985 to 1990. Preliminary estimates for 1991 have also been included, whenever data were available.

Not Available

1993-11-10T23:59:59.000Z

129

Coherence Length of Cold Exciton Gases in Coupled Quantum Wells  

Science Journals Connector (OSTI)

A Mach-Zehnder interferometer with spatial and spectral resolution was used to probe spontaneous coherence in cold exciton gases, which are implemented experimentally in the ring of indirect excitons in coupled quantum wells. A strong enhancement of the exciton coherence length is observed at temperatures below a few Kelvin. The increase of the coherence length is correlated with the macroscopic spatial ordering of excitons. The coherence length at the lowest temperature corresponds to a very narrow spread of the exciton momentum distribution, much smaller than that for a classical exciton gas.

Sen Yang, A. T. Hammack, M. M. Fogler, L. V. Butov, and A. C. Gossard

2006-10-31T23:59:59.000Z

130

Emissions Of Greenhouse Gases From Rice Agriculture  

SciTech Connect

This project produced detailed data on the processes that affect methane and nitrous oxide emissions from rice agriculture and their inter-relationships. It defines the shifting roles and potential future of these gases in causing global warming and the benefits and tradeoffs of reducing emissions. The major results include: 1). Mechanisms and Processes Leading to Methane Emissions are Delineated. Our experiments have tested the standard model of methane emissions from rice fields and found new results on the processes that control the flux. A mathematical mass balance model was used to unravel the production, oxidation and transport of methane from rice. The results suggested that when large amounts of organic matter are applied, the additional flux that is observed is due to both greater production and reduced oxidation of methane. 2). Methane Emissions From China Have Been Decreasing Over the Last Two Decades. We have calculated that methane emissions from rice fields have been falling in recent decades. This decrease is particularly large in China. While some of this is due to reduced area of rice agriculture, the bigger effect is from the reduction in the emission factor which is the annual amount of methane emitted per hectare of rice. The two most important changes that cause this decreasing emission from China are the reduced use of organic amendments which have been replaced by commercial nitrogen fertilizers, and the increased practice of intermittent flooding as greater demands are placed on water resources. 3). Global Methane Emissions Have Been Constant For More Than 20 Years. While the concentrations of methane in the atmosphere have been leveling off in recent years, our studies show that this is caused by a near constant total global source of methane for the last 20 years or more. This is probably because as some anthropogenic sources have increased, others, such as the rice agriculture source, have fallen. Changes in natural emissions appear small. 4). Nitrous Oxide Emissions From Rice Fields Increase as Methane Emissions Drop. Inundated conditions favor anaerobic methane production with high emission rates and de-nitrification resulting in modest nitrous oxide emissions. Under drier conditions such as intermittent flooding, methane emissions fall and nitrous oxide emissions increase. Increased nitrogen fertilizer use increases nitrous oxide emissions and is usually accompanied by reduced organic matter applications which decreases methane emissions. These mechanisms cause a generally inverse relationship between methane and nitrous oxide emissions. Reduction of methane from rice agriculture to control global warming comes with tradeoffs with increased nitrous oxide emissions. 5). High Spatial Resolution Maps of Emissions Produced. Maps of methane and nitrous oxide emissions at a resolution of 5 min 5 min have been produced based on the composite results of this research. These maps are necessary for both scientific and policy uses.

M. Aslam K. Khalil

2009-07-16T23:59:59.000Z

131

Risk Removal | Department of Energy  

Energy Savers (EERE)

Risk Removal Risk Removal Workers safely remove old mercury tanks from the Y-12 National Security Complex. Workers safely remove old mercury tanks from the Y-12 National Security...

132

Combustion behavior of a spark ignition engine fueled with synthetic gases derived from biogas  

Science Journals Connector (OSTI)

Abstract Combustion results obtained from a spark ignition engine fueled with two synthetic gases obtained from catalytic decomposition of biogas are presented in this paper. These results are compared with those obtained when the engine was fueled with gasoline, methane and with the biogas from which synthetic gases are extracted. Experimental tests were performed under a wide range of speeds and at three equivalence ratios. Results showed that fractions of hydrogen in synthetic gases increased maximum pressures inside cylinder. Moreover, peak pressures were detected closer to top dead center than methane and biogas. Despite the fraction of diluents in the composition of synthetic gases, high speeds and lean conditions resulted in higher indicated efficiencies than those obtained with gasoline. Moreover, combustion speed and heat release rate were strongly influenced by the proportion of diluents and hydrogen in gaseous blends. CO and CO2 content in the composition of synthetic gases contributed to increase the exhaust concentrations of these pollutants compared with the other fuels, while HC decreased because of the small fraction of methane which remained unburned. Although \\{NOx\\} emissions were mitigated by diluents, like CO2 and air excess, high hydrogen fraction in composition of syngas involved elevated \\{NOx\\} emissions due to the increase in flame temperature that hydrogen produces.

J. Arroyo; F. Moreno; M. Muoz; C. Monn; N. Bernal

2014-01-01T23:59:59.000Z

133

Chemical Properties of the Rare Gases  

Science Journals Connector (OSTI)

... of argon of about 100 atm. I have already shown by an independent method1 that radon, too, forms a hydrate which is much more stable than those of other rare ... , forms a hydrate which is much more stable than those of other rare gases. Radon is easily held by crystals of sulphur dioxide hydrates, when they are formed from ...

B. A. NIKITIN

1937-10-09T23:59:59.000Z

134

New instruments for measuring landfill gases  

Science Journals Connector (OSTI)

New instruments for measuring landfill gases ... The legislation mandates that landfill operators monitor more than 1200 active sites for specific pollution products. ... According to Varian, the instrumentation systems can be adapted easily to meet landfill testing requirements that might be enacted in states other than California. ...

RUDY BAUM

1988-02-01T23:59:59.000Z

135

Pulsed Laser Deposition of Photoresponsive Two-Dimensional GaSe Nanosheet Networks  

SciTech Connect

Here we explore pulsed laser deposition (PLD), a well known and versatile synthesis method principally used for epitaxial oxide thin film growth, for the synthesis of functional metal chalcogenide (GaSe) nanosheet networks by stoichiometric transfer of laser vaporized material from bulk GaSe targets in Ar background gas. Uniform coverage of interconnected, crystalline, few-layer, photoresponsive GaSe nanosheets in both in-plane and out-of-plane orientations were achieved under different ablation plume conditions over ~1.5 cm2 areas. Plume propagation was characterized by in situ ICCD-imaging. High (1 Torr) Ar background gas pressures were found to be crucial for the stoichiometric growth of GaSe nanosheet networks. Individual 1-3 layer GaSe triangular nanosheets of ~ 200 nm domain size were formed within 30 laser pulses, coalescing to form nanosheet networks in as few as 100 laser pulses. The thickness of the deposited networks increased linearly with pulse number, adding layers in a two-dimensional (2D) growth mode while maintaining a surface roughness of 2 GaSe layers for increasing overall thickness. Field effect transistors using these interconnected crystalline GaSe networks showed p-type semiconducting characteristics with mobilities reaching as high as 0.1 cm2V-1s-1. Spectrally-resolved photoresponsivities and external quantum efficiencies ranged from 0.4 AW-1 and 100% at 700 nm, to 1.4 AW-1 and 600 % at 240 nm, respectively. Pulsed laser deposition under these conditions appears to provide a versatile and rapid approach to stoichiometrically transfer and deposit photoresponsive networks of 2D nanosheets with digital thickness control and substrate-scale uniformity for a variety of applications.

Mahjouri-Samani, Masoud [ORNL; Gresback, Ryan G [ORNL; Tian, Mengkun [ORNL; Puretzky, Alexander A [ORNL; Rouleau, Christopher M [ORNL; Eres, Gyula [ORNL; Ivanov, Ilia N [ORNL; Xiao, Kai [ORNL; McGuire, Michael A [ORNL; Duscher, Gerd [University of Tennessee, Knoxville (UTK); Geohegan, David B [ORNL

2014-01-01T23:59:59.000Z

136

Increasing Knowledge Increasing Knowledge 29  

E-Print Network (OSTI)

28 Increasing Knowledge Increasing Knowledge 29 Expanding Leadership 36 Building Partnerships 43 the world. The challenges ahead are large, but WSP is preparing to meet them by increasing knowledge, expanding leadership, building partnerships, and seeking solutions. #12;29 Increasing Knowledge Increasing

Fay, Noah

137

Perdido LF-Gase to Electricity | Department of Energy  

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

Perdido LF-Gase to Electricity Perdido LF-Gase to Electricity This presentation was given at the July 17, 2012, Community Renewable Energy Deployment webinar on successful landfill...

138

BOC Lienhwa Industrial Gases BOCLH | Open Energy Information  

Open Energy Info (EERE)

BOC Lienhwa Industrial Gases BOCLH BOC Lienhwa Industrial Gases BOCLH Jump to: navigation, search Name BOC Lienhwa Industrial Gases (BOCLH) Place Taipei, Taiwan Sector Solar Product BOCLH is a joint venture between the Lien Hwa Industrial Corporation and the BOC Group in the United Kingdom and produces high-purity gases used in solar component production. References BOC Lienhwa Industrial Gases (BOCLH)[1] LinkedIn Connections CrunchBase Profile No CrunchBase profile. Create one now! This article is a stub. You can help OpenEI by expanding it. BOC Lienhwa Industrial Gases (BOCLH) is a company located in Taipei, Taiwan . References ↑ "BOC Lienhwa Industrial Gases (BOCLH)" Retrieved from "http://en.openei.org/w/index.php?title=BOC_Lienhwa_Industrial_Gases_BOCLH&oldid=342956

139

Sorption of organic gases in residential bedrooms and bathrooms  

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

Sorption of organic gases in residential bedrooms and bathrooms Sorption of organic gases in residential bedrooms and bathrooms Title Sorption of organic gases in residential bedrooms and bathrooms Publication Type Conference Paper LBNL Report Number LBNL-56787 Year of Publication 2005 Authors Singer, Brett C., Alfred T. Hodgson, Toshifumi Hotchi, Katherine Y. Ming, Richard G. Sextro, Emily E. Wood, and Nancy J. Brown Conference Name Proceedings of the 10th International Conference on Indoor Air Quality and Climate - Indoor Air 2005 Volume 2(9) Publisher Tsinghua University Press Conference Location Beijing, China Abstract Experiments were conducted to characterize organic gas sorption in residential bedrooms (n=4), bathrooms (n=2), and a furnished test chamber. Rooms were studied "as-is" with material surfaces and furnishings unaltered. Surface materials were characterized and areas quantified. Experiments included rapid volatilization of a volatile organic compound (VOC) mixture with the room closed and sealed for a 5-h Adsorb phase, followed by 30-min Flush and 2-h closed-room Desorb phases. The mixture included n-alkanes, aromatics, glycol ethers, 2-ethyl-1-hexanol, dichlorobenzene, and organophosphorus compounds. Measured gas-phase concentrations were fit to three variations of a mathematical model that considers sorption occurring at one surface sink and one potential embedded sink. The 2-parameter sink model tracked measurements for most compounds, but improved fits were obtained for some VOCs with a 3-parameter sink-diffusion or a 4-parameter two-sink model. Sorptive partitioning and initial adsorption rates increased with decreasing vapour pressure within each chemical class.

140

Impact of increasing MHTGR power on passive heat removal  

SciTech Connect

In 1990 a cost reduction study recommended that the reference US MHTGR module design be changed to an 84-column, 450 MW(t) annular reactor core to attain improved economics with the same high level of safety as the previous reference 66-column, 350 MW(t) MHTGR module. The objective of this paper is to report on a recently completed core configuration trade study that reviewed the basis for that recommendation with more detailed assessments. The trade study examined alternate core configurations in terms of the size, shape, and power level. Core configurations at 450 MW(t), an alterative at higher power, and one at lower power were considered. These alternatives represented the maximum achievable power for fuel element for two different reactor vessel sizes. Fuel, reactor internal and vessel temperatures during pressurized and depressurized conduction cooldown transients are presented and compared to limits. Based on the need to improve economics without sacrificing the MHTGR`s high level of safety, the trade study confirmed that the previously selected 84-column, 450 MW(t) annular design remains the preferable configuration.

Dunn, T.D.; Schwartz, A.A.; Silady, F.A.

1992-07-01T23:59:59.000Z

Note: This page contains sample records for the topic "gases removed increased" 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

Impact of increasing MHTGR power on passive heat removal  

SciTech Connect

In 1990 a cost reduction study recommended that the reference US MHTGR module design be changed to an 84-column, 450 MW(t) annular reactor core to attain improved economics with the same high level of safety as the previous reference 66-column, 350 MW(t) MHTGR module. The objective of this paper is to report on a recently completed core configuration trade study that reviewed the basis for that recommendation with more detailed assessments. The trade study examined alternate core configurations in terms of the size, shape, and power level. Core configurations at 450 MW(t), an alterative at higher power, and one at lower power were considered. These alternatives represented the maximum achievable power for fuel element for two different reactor vessel sizes. Fuel, reactor internal and vessel temperatures during pressurized and depressurized conduction cooldown transients are presented and compared to limits. Based on the need to improve economics without sacrificing the MHTGR's high level of safety, the trade study confirmed that the previously selected 84-column, 450 MW(t) annular design remains the preferable configuration.

Dunn, T.D.; Schwartz, A.A.; Silady, F.A.

1992-07-01T23:59:59.000Z

142

Tritium Removal from Carbon Plasma Facing Components  

SciTech Connect

Tritium removal is a major unsolved development task for next-step devices with carbon plasma-facing components. The 2-3 order of magnitude increase in duty cycle and associated tritium accumulation rate in a next-step tokamak will place unprecedented demands on tritium removal technology. The associated technical risk can be mitigated only if suitable removal techniques are demonstrated on tokamaks before the construction of a next-step device. This article reviews the history of codeposition, the tritium experience of TFTR (Tokamak Fusion Test Reactor) and JET (Joint European Torus) and the tritium removal rate required to support ITER's planned operational schedule. The merits and shortcomings of various tritium removal techniques are discussed with particular emphasis on oxidation and laser surface heating.

C.H. Skinner; J.P. Coad; G. Federici

2003-11-24T23:59:59.000Z

143

On the ratio of the shear viscosity to the density of entropy of the rare gases and , and  

Science Journals Connector (OSTI)

Abstract The ratio ? of the shear viscosity ? to the volume density of entropy s , ? = ? / s , of the rare gases He, Ne, Ar, Kr, and Xe and the molecules H 2 , N 2 , CH 4 , and CF 4 is studied in the critical region. It is shown that the minimum value ? m of ? / s is observed in the vicinity of the critical point. In addition the universal inequality ? ? ? / ( 4 ? k ) proposed by Kovtun, Son, and Starinets [Phys. Rev. Lett. 94 (2005) 111601] holds for these gases. For the rare gases and 6Li ? m depends linearly on m 1 / 2 ? 2 , where m is the mass and ? defined via the potential energy function as U ( ? ) = 0 . ? m of the molecules H 2 , N 2 , CH 4 , and CF 4 falls on the same straight line provided that the vibrational and rotational contributions to the entropy density s are removed.

U. Hohm

2014-01-01T23:59:59.000Z

144

Selective Catalytic Oxidation of Hydrogen Sulfide to Elemental Sulfur from Coal-Derived Fuel Gases  

SciTech Connect

The development of low cost, highly efficient, desulfurization technology with integrated sulfur recovery remains a principle barrier issue for Vision 21 integrated gasification combined cycle (IGCC) power generation plants. In this plan, the U. S. Department of Energy will construct ultra-clean, modular, co-production IGCC power plants each with chemical products tailored to meet the demands of specific regional markets. The catalysts employed in these co-production modules, for example water-gas-shift and Fischer-Tropsch catalysts, are readily poisoned by hydrogen sulfide (H{sub 2}S), a sulfur contaminant, present in the coal-derived fuel gases. To prevent poisoning of these catalysts, the removal of H{sub 2}S down to the parts-per-billion level is necessary. Historically, research into the purification of coal-derived fuel gases has focused on dry technologies that offer the prospect of higher combined cycle efficiencies as well as improved thermal integration with co-production modules. Primarily, these concepts rely on a highly selective process separation step to remove low concentrations of H{sub 2}S present in the fuel gases and produce a concentrated stream of sulfur bearing effluent. This effluent must then undergo further processing to be converted to its final form, usually elemental sulfur. Ultimately, desulfurization of coal-derived fuel gases may cost as much as 15% of the total fixed capital investment (Chen et al., 1992). It is, therefore, desirable to develop new technology that can accomplish H{sub 2}S separation and direct conversion to elemental sulfur more efficiently and with a lower initial fixed capital investment.

Gardner, Todd H.; Berry, David A.; Lyons, K. David; Beer, Stephen K.; Monahan, Michael J.

2001-11-06T23:59:59.000Z

145

Continuous sulfur removal process  

DOE Patents (OSTI)

A continuous process for the removal of hydrogen sulfide from a gas stream using a membrane comprising a metal oxide deposited on a porous support is disclosed. 4 figures.

Jalan, V.; Ryu, J.

1994-04-26T23:59:59.000Z

146

Using carbon adsorbents for removing nitrogen oxides and sulphur oxides from flue gases  

Science Journals Connector (OSTI)

The use of carbon adsorbents in industrial power engineering outside Russia is briefly reviewed and the results of our own experimental investigations, made in the laboratory and at a pilot commercial installation, are given. The proposal to use the described device in a KE-25-24-C industrial boiler is outlined.

A.I. Blokhin; A.N. Nikitin; A.O. Gabibov

2003-01-01T23:59:59.000Z

147

U.S. Nonhydrocarbon Gases Removed from Natural Gas (Million Cubic Feet)  

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

Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec Year Jan Feb Mar Apr May Jun Jul Aug Sep Oct Nov Dec 1973 NA NA NA NA NA NA NA NA NA NA NA NA 1974 NA NA NA NA NA NA NA NA NA NA NA NA 1975 NA NA NA NA NA NA NA NA NA NA NA NA 1976 NA NA NA NA NA NA NA NA NA NA NA NA 1977 NA NA NA NA NA NA NA NA NA NA NA NA 1978 NA NA NA NA NA NA NA NA NA NA NA NA 1979 NA NA NA NA NA NA NA NA NA NA NA NA 1980 18,000 16,000 17,000 16,000 17,000 16,000 17,000 17,000 17,000 15,000 17,000 18,000 1981 20,000 18,000 18,000 18,000 18,000 19,000 20,000 18,000 18,000 18,000 17,000 20,000 1982 19,000 18,000 19,000 18,000 17,000 16,000 15,000 18,000 16,000 16,000 18,000 19,000 1983 19,994 16,995 17,995 15,995 16,995 18,995 17,995 19,994 18,995 17,995 18,995 20,994

148

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

DOE Patents (OSTI)

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

Apel, William A. (Idaho Falls, ID)

1998-01-01T23:59:59.000Z

149

Theoretical Gas Phase Mass Transfer Coefficients for Endogenous Gases in the Lungs  

E-Print Network (OSTI)

Theoretical Gas Phase Mass Transfer Coefficients for Endogenous Gases in the Lungs PETER CONDORELLI of California at Irvine, Irvine, CA (Received 18 November 1997; accepted 9 February 1999) Abstract--Gas phase in terms of a lumped variable, Per(L/D)n . (Sh) increases as the solu- bility of the gas in tissue

George, Steven C.

150

ESTABoues, a decision tool to assess greenhouse gases of sewage sludge treatment and di  

E-Print Network (OSTI)

digestion, aerobic digestion, dewatering, al composting, drying) and sludge disposal route (land applicationORBIT2012 G ESTABoues, a decision tool to assess greenhouse gases of sewage sludge treatment and di-laure.reverdy@irstea.fr EXECUTIVE SUMMARY Sewage sludge production increases continuously reaching almost 20% (946 700 t 1 118 795

Paris-Sud XI, Université de

151

Separation of rare gases and chiral molecules by selective binding in porous organic cages  

SciTech Connect

Abstract: The rare gases krypton, xenon, and radon pose both an economic opportunity and a potential environmental hazard. Xenon is used in commercial lighting, medical imaging, and anesthesia, and can sell for $5,000 per kilogram. Radon, by contrast, Is naturally radioactive and the second largest cause of lung cancer, and radioactive xenon, 133Xe, was a major pollutant released In the Fukushima Daiichi Nuclear Power Plant disaster. We describe an organic cage molecule that can capture xenon and radon with unprecedented selectivity, suggesting new technologies for environmental monitoring, removal of pollutants, or the recovery of rare, valuable elements from air.

Chen, Linjiang; Reiss, Paul S.; Chong, Samantha Y.; Holden, Daniel; Jelfs, Kim E.; Hasell, Tom; Little, Marc A.; Kewley, Adam; Briggs, Michael E.; Stephenson, Andrew; Thomas, K. M.; Armstrong, Jayne A.; Bell, Jon; Busto, Jose; Noel, Raymond; Liu, Jian; Strachan, Denis M.; Thallapally, Praveen K.; Cooper, Andrew I.

2014-10-31T23:59:59.000Z

152

Two-stage air gasification of mixed plastic waste: Olivine as the bed material and effects of various additives and a nickel-plated distributor on the tar removal  

Science Journals Connector (OSTI)

Abstract Air gasification of mixed plastic waste was conducted in a two-stage gasifier. The effects of the combination of olivine as the fluidized bed material and activated carbon with or without other additives for tar cracking, as well as a Ni-plated distributor, the use of steam as a gasifying agent, and the calcination of olivine on the producer gas compositions and tar production, were also investigated. The maximum H2 concentration (27.3vol%) was obtained with 900g of activated carbon in the tar-cracking zone, and through the use of calcined olivine as the bed material. In the experiments, the maximum tar removal efficiency calculated using a base case reached 98.2%. The \\{LHVs\\} of the producer gases were in the range of 6.19.0MJ/Nm3. The increase in the activated carbon amount led to an enhanced H2 production, as well as a decrease in tar production. The Ni-plated distributor was found to be effective for tar removal. In the application of dolomite in the tar-cracking zone and the use of steam as a fluidizing medium resulted in a high rate of \\{HCl\\} removal. The minimum \\{HCl\\} concentration in the producer gases was under 1ppm.

Min-Hwan Cho; Tae-Young Mun; Young-Kon Choi; Joo-Sik Kim

2014-01-01T23:59:59.000Z

153

Drum lid removal tool  

DOE Patents (OSTI)

A tool for removing the lid of a metal drum wherein the lid is clamped over the drum rim without protruding edges, the tool having an elongated handle with a blade carried by an angularly positioned holder affixed to the midsection of the handle, the blade being of selected width to slice between lid lip and the drum rim and, when the blade is so positioned, upward motion of the blade handle will cause the blade to pry the lip from the rim and allow the lid to be removed.

Pella, Bernard M. (Martinez, GA); Smith, Philip D. (North Augusta, SC)

2010-08-24T23:59:59.000Z

154

Efficieny handling effluent gases through chemical scrubbing  

SciTech Connect

This paper is presented as an information source for efficiencies of chemical scrubbing. In it, we will discuss the specific problems of scrubbing silane, disilane, diborane, phosphine, hydrogen selenide and arsine. We will explain the scrubber dynamics, gases and flow rates used along with liquid mediums. The equipment and procedures used for testing, as well as the determination of the results, will be discussed. We intend to give examples of possible reactions and documentation of our efficiencies. Installation and maintenance will be touched, as well as our experiments into accidental catastrophic releases. From all of this we will derive conclusions as to the best possible means of wet chemical scrubbing.

Herman, T.; Soden, S.

1988-07-15T23:59:59.000Z

155

Heat conduction in relativistic neutral gases revisited  

E-Print Network (OSTI)

The kinetic theory of dilute gases to first order in the gradients yields linear relations between forces and fluxes. The heat flux for the relativistic gas has been shown to be related not only to the temperature gradient but also to the density gradient in the representation where number density, temperature and hydrodynamic velocity are the independent state variables. In this work we show the calculation of the corresponding transport coefficients from the full Boltzmann equation and compare the magnitude of the relativistic correction.

A. L. Garcia-Perciante; A. R. Mendez

2010-09-30T23:59:59.000Z

156

Assess Potential Agency Size Changes that Impact Greenhouse Gases from  

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

Vehicles and Mobile Equipment Vehicles and Mobile Equipment Assess Potential Agency Size Changes that Impact Greenhouse Gases from Vehicles and Mobile Equipment October 7, 2013 - 11:31am Addthis YOU ARE HERE Step 1 Planned changes in a Federal agency's size, missions, transportation needs, and vehicle inventory all impact the strategic portfolio planning efforts that target greenhouse gas (GHG) emissions mitigation for vehicles and mobile equipment. Under Section 142 of the Energy Independence and Security Act (EISA) and Section 8 of Executive Order (E.O.) 13514, agencies are required to develop a plan that will reduce fleet GHG emissions to meet Federally mandated petroleum reduction and alternative fuel increase targets. Agencies can use these plans as a basis for determining potential changes in fleet size and

157

Trace gases, CO2, climate, and the greenhouse effect  

Science Journals Connector (OSTI)

Weather is driven by the suns energy input and the difference between insolation per unit area of the poles and the equator. The energy flux of the Earth is in long?term balanceas much is radiated away by the Earth as is absorbed or the mean temperature would have to increase or decrease steadily (and of course this is not observed). CO2 and other trace gases can cause the Earths mean temperature to rise through the Greenhouse Effect. The mean temperature in the Little Ice Age was only 1?C cooler but large effects were felt especially toward the poles. The CO2 which stays in the atmosphere will raise Earths mean temperature with effects which are relatively certain: a lot of warming at the poles and a very small amount of warming at the equator.

Gordon J. Aubrecht II

1988-01-01T23:59:59.000Z

158

EIA-Voluntary Reporting of Greenhouse Gases Program - Greenhouse Gases and  

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

Greenhouse Gases and Global Warming Potentials (GWP) Greenhouse Gases and Global Warming Potentials (GWP) Voluntary Reporting of Greenhouse Gases Program Greenhouse Gases and Global Warming Potentials (GWP) (From Appendix E of the instructions to Form EIA-1605) GREENHOUSE GAS NAME GREENHOUSE GAS CODE FORMULA GWP TAR1 AR42 (1) Carbon Dioxide CO2 CO2 1 1 (2) Methane CH4 CH4 23 25 (3) Nitrous Oxide N2O N2O 296 298 (4) Hydroflourocarbons HFC-23 (trifluoromethane) 15 CHF3 12000 14800 HFC-32 (difluoromethane) 16 CH2F2 550 675 HFC-41 (monofluoromethane) 43 CH3F 97 -3 HFC-125 (pentafluoroethane) 17 CHF2CF3 3400 3500 HFC-134 (1,1,2,2-tetrafluoroethane) 44 CHF2CHF2 1100 -3 HFC-134a (1,1,1,2-tetrafluoroethane) 18 CH2FCF3 1300 1430 HFC-143 (1,1,2-trifluorethane) 45 CHF2CH2F 330 -3 HFC-143a (1,1,1-trifluoroethane) 46 CF3CH3 4300 4470 HFC-152 (1,2-difluorethane) 47 CH2FCH2F

159

Condensate removal device  

DOE Patents (OSTI)

A condensate removal device is disclosed which incorporates a strainer in unit with an orifice. The strainer is cylindrical with its longitudinal axis transverse to that of the vapor conduit in which it is mounted. The orifice is positioned inside the strainer proximate the end which is remoter from the vapor conduit.

Maddox, James W. (Newport News, VA); Berger, David D. (Alexandria, VA)

1984-01-01T23:59:59.000Z

160

Removal of 2-Aminophenol Using Novel Adsorbents  

Science Journals Connector (OSTI)

The positive values of entropy show the increased randomness at solid/solution interface with some structural changes in the adsorbate and adsorbent and the affinity of adsorbents toward 2AP. ... Upon doubling the adsorbent amount from 10 to 20 g/L, the amount of phenol adsorbed also increases by almost two-fold. ... It is quite evident that, after 6 h of equilibrium, 27% of the total 2-aminophenol is removed by 10 g/L of the adsorbent slag, while 20 g/L of slag removed 37% of 2-aminophenol and 30 g/L of adsorbent adsorbs 42% under identical experimental conditions. ...

Vinod K. Gupta; Dinesh Mohan; Suhas; Kunwar P. Singh

2006-01-04T23:59:59.000Z

Note: This page contains sample records for the topic "gases removed increased" 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

The greenhouse gases HFCs, PFCs Danish consumption and emissions, 2007  

E-Print Network (OSTI)

The greenhouse gases HFCs, PFCs and SF6 Danish consumption and emissions, 2007 Tomas Sander Poulsen AND EMISSION OF F-GASES 7 1.1.1 Consumption 7 1.1.2 Emission 7 1.1.3 Trends in total GWP contribution from F 21 4 EMISSION OF F-GASES 23 4.1.1 Emissions of HFCs from refrigerants 23 4.1.2 Emissions of HFCs from

162

Suspended two-dimensional electron and hole gases  

SciTech Connect

We report on the fabrication of fully suspended two-dimensional electron and hole gases in III-V heterostructures. Low temperature transport measurements verify that the properties of the suspended gases are only slightly degraded with respect to the non-suspended gases. Focused ion beam technology is used to pattern suspended nanostructures with minimum damage from the ion beam, due to the small width of the suspended membrane.

Kazazis, D.; Bourhis, E.; Gierak, J.; Gennser, U. [Laboratoire de Photonique et de Nanostructures, CNRS-LPN, Route de Nozay, 91460 Marcoussis (France); Bourgeois, O. [Institut Nel, CNRS-UJF, BP 166, 38042 Grenoble Cedex 9 (France); Antoni, T. [Laboratoire de Photonique et de Nanostructures, CNRS-LPN, Route de Nozay, 91460 Marcoussis, France and Laboratoire Kastler Brossel, Universit Pierre et Marie Curie, 4 Place Jussieu, 75005 Paris (France)

2013-12-04T23:59:59.000Z

163

EIA-Voluntary Reporting of Greenhouse Gases Program - Emission...  

Gasoline and Diesel Fuel Update (EIA)

AP-42 Volume 2 mobile sources Global Warming Potentials The Intergovernmental Panel on Climate Change (IPCC) revised GWPs for certain greenhouse gases in 2007 for the Fourth...

164

Energetic Materials for EGS Well Stimulation (solids, liquids, gases)  

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

Energetic Materials for EGS Well Stimulation (solids, liquids, gases) presentation at the April 2013 peer review meeting held in Denver, Colorado.

165

Gas geochemistry of the Valles caldera region, New Mexico and comparisons with gases at Yellowstone, Long Valley and other geothermal systems  

Science Journals Connector (OSTI)

Noncondensible gases from hot springs, fumaroles, and deep wells within the Valles caldera geothermal system (210300C) consist of roughly 98.5 mol% CO2, 0.5 mol% H2S, and 1 mol% other components. 3He/4He ratios indicate a deep magmatic source (R/Ra up to 6) whereas ?13CCO2 values (?3 to ?5) do not discriminate between a mantle/magmatic source and a source from subjacent, hydrothermally altered Paleozoic carbonate rocks. Regional gases from sites within a 50-km radius beyond Valles caldera are relatively enriched in CO2 and He, but depleted in H2S compared to Valles gases. Regional gases have R/Ra values ?1.2 due to more interaction with the crust and/or less contribution from the mantle. Carbon sources for regional CO2 are varied. During 19821998, repeat analyses of gases from intracaldera sites at Sulphur Springs showed relatively constant CH4, H2, and H2S contents. The only exception was gas from Footbath Spring (19871993), which experienced increases in these three components during drilling and testing of scientific wells VC-2a and VC-2b. Present-day Valles gases contain substantially less N2 than fluid inclusion gases trapped in deep, early-stage, post-caldera vein minerals. This suggests that the long-lived Valles hydrothermal system (ca. 1 Myr) has depleted subsurface Paleozoic sedimentary rocks of nitrogen. When compared with gases from many other geothermal systems, Valles caldera gases are relatively enriched in He but depleted in CH4, N2 and Ar. In this respect, Valles gases resemble end-member hydrothermal and magmatic gases discharged at hot spots (Galapagos, Kilauea, and Yellowstone).

Fraser Goff; Cathy J. Janik

2002-01-01T23:59:59.000Z

166

DOE Removes Brookhaven Contractor  

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

DOE Removes DOE Removes Brookhaven Contractor Peña sends a message to DOE facilities nationwide INSIDE 2 Accelerator Rx 4 FermiKids 6 Spring at Fermilab Photos courtesy of Brookhaven National Laboratory by Judy Jackson, Office of Public Affairs Secretary of Energy Federico Peña announced on Thursday, May 1, that the Department of Energy would immediately terminate the current management contract with Associated Universities, Inc. at Brookhaven National Laboratory in Upton, New York. Peña said that he made the decision after receiving the results of a laboratory safety management review conducted by the independent oversight arm of DOE's Office of Environment, Safety and Health. In addition, the Secretary said he found unacceptable "the continued on page 8 Volume 20 Friday, May 16, 1997

167

Pneumatic soil removal tool  

DOE Patents (OSTI)

A soil removal tool is provided for removing radioactive soil, rock and other debris from the bottom of an excavation, while permitting the operator to be located outside of a containment for that excavation. The tool includes a fixed jaw, secured to one end of an elongate pipe, which cooperates with a movable jaw pivotably mounted on the pipe. Movement of the movable jaw is controlled by a pneumatic cylinder mounted on the pipe. The actuator rod of the pneumatic cylinder is connected to a collar which is slidably mounted on the pipe and forms part of the pivotable mounting assembly for the movable jaw. Air is supplied to the pneumatic cylinder through a handle connected to the pipe, under the control of an actuator valve mounted on the handle, to provide movement of the movable jaw. 3 figs.

Neuhaus, J.E.

1992-10-13T23:59:59.000Z

168

On surface temperature, greenhouse gases, and aerosols: models and observations  

SciTech Connect

The effect of changes in atmospheric carbon dioxide concentrations and sulphate aerosols on near-surface temperature is investigated using a version of the Hadley Centre atmospheric model coupled to a mixed layer ocean. The scattering of sunlight by sulphate aerosols is represented by appropriately enhancing the surface albedo. On doubling atmospheric carbon dioxide concentrations, the global mean temperature increases by 5.2 K. An integration with a 39% increase in CO{sub 2}, giving the estimated change in radiative heating due to increases in greenhouse gases since 1900, produced an equilibrium warming of 2.3 K, which, even allowing for oceanic inertia, is significantly higher than the observed warming over the same period. Furthermore, the simulation suggests a substantial warming everywhere, whereas the observations indicate isolated regions of cooling, including parts of the northern midlatitude continents. The addition of an estimate of the effect of scattering by current industrial aerosols (uncertain by a factor of at least 3) leads to improved agreement with the observed pattern of changes over the northern continents and reduces the global mean warming by about 30%. Doubling the aerosol forcing produces patterns that are still compatible with the observations, but further increase leads to unrealistically extensive cooling in the midlatitudes. The diurnal range of surface temperature decreases over most of the northern extratropics on increasing CO{sub 2}, in agreement with recent observations. The addition of the current industrial aerosol had little detectable effect on the diurnal range in the model because the direct effect of reduced solar heating at the surface is approximately balanced by the indirect effects of cooling. Thus, the ratio of the reduction in diurnal range to the mean warming is increased, in closer agreement with observations. Results from further sensitivity experiments with larger increases in aerosol and CO{sub 2} are presented.

Mitchell, J.F.B.; Davis, R.A.; Ingram, W.J.; Senior, C.A. [Hadley Centre for Climate Prediction and Research, Berkshire (United Kingdom)] [Hadley Centre for Climate Prediction and Research, Berkshire (United Kingdom)

1995-10-01T23:59:59.000Z

169

FLAMMABILITY CHARACTERISTICS OF COMBUSTIBLE GASES AND VAPORS  

Office of Scientific and Technical Information (OSTI)

Bulletin 627 Bulletin 627 BUREAU o b MINES FLAMMABILITY CHARACTERISTICS OF COMBUSTIBLE GASES AND VAPORS By Michael G. Zabetakis DISCLAIMER This report was prepared as an account of work sponsored by an agency of the United States Government. Neither the United States Government nor any agency Thereof, nor any of their employees, makes any warranty, express or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any information, apparatus, product, or process disclosed, or represents that its use would not infringe privately owned rights. Reference herein to any specific commercial product, process, or service by trade name, trademark, manufacturer, or otherwise does not necessarily constitute or imply its endorsement,

170

Refinery Yield of Liquefied Refinery Gases  

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

Refinery Yield Refinery Yield (Percent) Product: Liquefied Refinery Gases Finished Motor Gasoline Finished Aviation Gasoline Kerosene-Type Jet Fuel Kerosene Distillate Fuel Oil Residual Fuel Oil Naphtha for Petrochemical Feedstock Use Other Oils for Petrochemical Feedstock Use Special Naphthas Lubricants Waxes Petroleum Coke Asphalt and Road Oil Still Gas Miscellaneous Products Processing Gain(-) or Loss(+) Period: Monthly Annual Download Series History Download Series History Definitions, Sources & Notes Definitions, Sources & Notes Show Data By: Product Area Apr-13 May-13 Jun-13 Jul-13 Aug-13 Sep-13 View History U.S. 5.3 5.4 5.2 5.2 5.1 3.9 1993-2013 PADD 1 4.4 5.1 4.9 4.9 4.6 2.1 1993-2013 East Coast 4.4 5.3 5.1 5.1 4.9 2.2 1993-2013

171

Shortcuts to adiabaticity for trapped ultracold gases  

E-Print Network (OSTI)

We study, experimentally and theoretically, the controlled transfer of harmonically trapped ultracold gases between different quantum states. In particular we experimentally demonstrate a fast decompression and displacement of both a non-interacting gas and an interacting Bose-Einstein condensate which are initially at equilibrium. The decompression parameters are engineered such that the final state is identical to that obtained after a perfectly adiabatic transformation despite the fact that the fast decompression is performed in the strongly non-adiabatic regime. During the transfer the atomic sample goes through strongly out-of-equilibrium states while the external confinement is modified until the system reaches the desired stationary state. The scheme is theoretically based on the invariants of motion and scaling equations techniques and can be generalized to decompression trajectories including an arbitrary deformation of the trap. It is also directly applicable to arbitrary initial non-equilibrium sta...

Schaff, Jean-Franois; Labeyrie, Guillaume; Vignolo, Patrizia

2011-01-01T23:59:59.000Z

172

Shortcuts to adiabaticity for trapped ultracold gases  

E-Print Network (OSTI)

We study, experimentally and theoretically, the controlled transfer of harmonically trapped ultracold gases between different quantum states. In particular we experimentally demonstrate a fast decompression and displacement of both a non-interacting gas and an interacting Bose-Einstein condensate which are initially at equilibrium. The decompression parameters are engineered such that the final state is identical to that obtained after a perfectly adiabatic transformation despite the fact that the fast decompression is performed in the strongly non-adiabatic regime. During the transfer the atomic sample goes through strongly out-of-equilibrium states while the external confinement is modified until the system reaches the desired stationary state. The scheme is theoretically based on the invariants of motion and scaling equations techniques and can be generalized to decompression trajectories including an arbitrary deformation of the trap. It is also directly applicable to arbitrary initial non-equilibrium states.

Jean-Franois Schaff; Pablo Capuzzi; Guillaume Labeyrie; Patrizia Vignolo

2011-05-11T23:59:59.000Z

173

Voluntary reporting of greenhouse gases 1997  

SciTech Connect

The Voluntary Reporting of Greenhouse Gases Program, required by Section 1605(b) of the Energy Policy Act of 1992, records the results of voluntary measures to reduce, avoid, or sequester greenhouse gas emissions. In 1998, 156 US companies and other organizations reported to the Energy information Administration that, during 1997, they had achieved greenhouse gas emission reductions and carbon sequestration equivalent to 166 million tons of carbon dioxide, or about 2.5% of total US emissions for the year. For the 1,229 emission reduction projects reported, reductions usually were measured by comparing an estimate of actual emissions with an estimate of what emissions would have been had the project not been implemented.

NONE

1999-05-01T23:59:59.000Z

174

Bogoliubov spectrum of interacting Bose gases  

E-Print Network (OSTI)

We study the large-N limit of a system of N bosons interacting with a potential of intensity 1/N. When the ground state energy is to the first order given by Hartree's theory, we study the next order, predicted by Bogoliubov's theory. We show the convergence of the lower eigenvalues and eigenfunctions towards that of the Bogoliubov Hamiltonian (up to a convenient unitary transform). We also prove the convergence of the free energy when the system is sufficiently trapped. Our results are valid in an abstract setting, our main assumptions being that the Hartree ground state is unique and non-degenerate, and that there is complete Bose-Einstein condensation on this state. Using our method we then treat two applications: atoms with ''bosonic'' electrons on one hand, and trapped 2D and 3D Coulomb gases on the other hand.

Mathieu Lewin; Phan Thnh Nam; Sylvia Serfaty; Jan Philip Solovej

2014-03-11T23:59:59.000Z

175

Lead removal by using carbon nanotubes  

Science Journals Connector (OSTI)

Exposure to lead (Pb) can cause anemia, diseases of the liver and kidneys, brain damage and ultimately death. For these reasons, heavy metals must be removed as much as possible from water. The removal of Pb (II) ions from aqueous solution using carbon nanotubes (CNT) as the adsorbent was investigated. The effects of pH were studied at 25C. Batch mode adsorption study has revealed that the removal of Pb (II) ions was maximum (85% removal) at pH 5 and achieved 83% removal at 40 mg/L of CNTs. The adsorption continuously increased in the pH range of 3-5, beyond which the adsorption could not be carried out due to the precipitation of metal. This study was also supported by characterisation of CNTs using FESEM. The characterisation suggested that at acidic condition (pH 5), the surfaces of CNTs are more aligned and well-integrated compared to CNTs at different pHs. Finally, it can be concluded that CNTs could be a potential adsorbent for the removal of Pb from wastewater.

A.A. Muataz; M. Fettouhi; A. Al-Mammum; N. Yahya

2009-01-01T23:59:59.000Z

176

1988 Pilot Institute on Global Change on trace gases and the biosphere  

SciTech Connect

This proposal seeks multi-agency funding to conduct an international, multidisciplinary 1988 Pilot Institute on Global Change to take place from August 7 through 21, 1988, on the topic: Trace Gases and the Biosphere. The institute, to be held in Snowmass, Colorado, is envisioned as a pilot version of a continuing series of institutes on Global Change (IGC). This proposal seeks support for the 1988 pilot institute only. The concept and structure for the continuing series, and the definition of the 1988 pilot institute, were developed at an intensive and multidisciplinary Summer Institute Planning Meeting in Boulder, Colorado, on August 24--25, 1987. The theme for the 1988 PIGC, Trace Gases and the Biosphere, will focus a concerted, high-level multidisciplinary effort on a scientific problem central to the Global Change Program. Dramatic year-to-year increases in the global concentrations of radiatively-active trace gases such as methane and carbon dioxide are now well documented. The predicted climatic effects of these changes lend special urgency to efforts to study the biospheric sources and sinks of these gases and to clarify their interactions and role in the geosphere-biosphere system.

Eddy, J.A.; Moore, B. III

1998-07-01T23:59:59.000Z

177

OBTAINING LAWS OF THERMODYNAMICS FOR IDEAL GASES USING ELASTIC COLLISIONS  

E-Print Network (OSTI)

OBTAINING LAWS OF THERMODYNAMICS FOR IDEAL GASES USING ELASTIC COLLISIONS STEPHEN MONTGOMERY law of expansion of ideal gases. 1. The Second Law of Thermodynamics A thermally isolated container-SMITH AND HANNAH MORGAN Abstract. The purpose of this note is to see to what extent ideal gas laws can be obtained

Montgomery-Smith, Stephen

178

EIA - Greenhouse Gas Emissions - High-GWP gases  

Gasoline and Diesel Fuel Update (EIA)

5. High-GWP gases 5. High-GWP gases 5.1. Total emissions Greenhouse gases with high global warming potential (high-GWP gases) are hydrofluorocarbons (HFCs), perfluorocarbons (PFCs), and sulfur hexafluoride (SF6), which together represented 3 percent of U.S. greenhouse gas emissions in 2009. Emissions estimates for the high-GWP gases are provided to EIA by the EPA's Office of Air and Radiation. The estimates for emissions of HFCs not related to industrial processes or electric transmission are derived from the EPA Vintaging Model. Emissions from manufacturing and utilities are derived by the EPA from a mix of public and proprietary data, including from the EPA's voluntary emission reduction partnership programs. For this year's EIA inventory, 2008 values for HFC-23 from HCFC-22

179

The Greenhouse Gases, Regulated Emissions, and Energy Use in Transportation  

Open Energy Info (EERE)

Gases, Regulated Emissions, and Energy Use in Transportation Gases, Regulated Emissions, and Energy Use in Transportation Model (GREET) Jump to: navigation, search Tool Summary Name: The Greenhouse Gases, Regulated Emissions, and Energy Use in Transportation Model (GREET Fleet) Agency/Company /Organization: Argonne National Laboratory Sector: Energy Focus Area: Greenhouse Gas, Transportation Phase: Determine Baseline, Evaluate Options Topics: Baseline projection, GHG inventory Resource Type: Software/modeling tools User Interface: Spreadsheet Website: greet.es.anl.gov/main Cost: Free OpenEI Keyword(s): EERE tool, The Greenhouse Gases, Regulated Emissions, and Energy Use in Transportation Model, GREET References: GREET Fleet Main Page[1] Logo: The Greenhouse Gases, Regulated Emissions, and Energy Use in Transportation Model (GREET Fleet)

180

EIA-Voluntary Reporting of Greenhouse Gases Program  

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

of Greenhouse Gases Program of Greenhouse Gases Program Voluntary Reporting of Greenhouse Gases Program ***THE VOLUNTARY REPORTING OF GREENHOUSE GASES ("1605(b)") PROGRAM HAS BEEN SUSPENDED.*** This affects all survey respondents. Please visit the What's New page for full details. What Is the Voluntary Reporting Program? logo Established by Section 1605(b) of the Energy Policy Act of 1992, the Voluntary Reporting of Greenhouse Gases Program encourages corporations, government agencies, non-profit organizations, households, and other private and public entities to submit annual reports of their greenhouse gas emissions, emission reductions, and sequestration activities. The Program provides a means for voluntary reporting that is complete, reliable, and consistent. More information on the program...

Note: This page contains sample records for the topic "gases removed increased" 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

Ordered Vertex Removal Subgraph Problems  

E-Print Network (OSTI)

of the vertex removal and subgraph problems are shown to be P­complete. In addition, a natural lex­ icographicOrdered Vertex Removal and Subgraph Problems Ray Greenlaw Department of Computer Science University­8703196. #12; Vertex Removal and Graph Problems Ray Greenlaw Department of Computer Science FR­35

Greenlaw, Ray

182

Method for producing and treating coal gases  

DOE Patents (OSTI)

A method of generating a de-sulphurized volatile matter and a relatively low Btu gas includes the initial step of pyrolyzing coal to produce volatile matter and a char. The volatile matter is fed to a first de-sulphurizer containing a de-sulphurizing agent to remove sulphur therefrom. At the same time, the char is gasified to produce a relatively low Btu gas. The low Btu gas is fed to a second de-sulphurizer containing the de-sulphurizing agent to remove sulphur therefrom. A regenerator is provided for removing sulphur from the de-sulphurizing agent. Portions of the de-sulphurizing agent are moved among the first de-sulphurizer, the second de-sulphurizer, and the regenerator such that the regenerator regenerates the de-sulphurizing agent. Preferably, the portions of the de-sulphurizing agent are moved from the second de-sulphurizer to the first de-sulphurizer, from the first de-sulphurizer to the regenerator, and from the regenerator to the second de-sulphurizer.

Calderon, Albert (P.O. Box 126, Bowling Green, OH 43402)

1990-01-01T23:59:59.000Z

183

Gases as Working Fluid in Parabolic Trough CSP Plants  

Science Journals Connector (OSTI)

Abstract The energetic dimension of actual economy is massively oriented towards the use of fossil fuels: they cover a share of 87% of the energy needs and the trend of this share is increasing, in spite of the commitments adopted by almost all the Countries in the World. Most crucial concern is CO2 levels in the atmosphere and the positive feedback between Earth's temperature increase and carbon. Actual technologies which make use of renewable sources seem to be not fully suitable to invert this continuous increase of fossil fuels. Concentrated Solar Power plants (CSP) have had, recently, a huge attention as a technology able to give, in the mean future, a strong contribution to the electrical energy generation. CSP technology has an intrinsic superiority with respect to the other renewable plants but actual plants suffer of many drawbacks which slow down a massive diffusion: these aspects increase costs and do not insure the reliability levels required to make the investments profitable. Gas as heat transfer fluid inside solar receiver in a CSP Parabolic Trough (PT) type plant is discussed in this paper: this would simplify actual technology in the conversion section, downstream the solar energy collecting phase. The use of gases calls for a new conversion section discussed in this paper based on a direct expansion in gas turbine plants. The success of this concept is related to the possibility to increase the fluid (gas) temperature above the actual operating maximum values. The paper discusses the performances of a new gas cycle, the performances of actual receivers when fed with gas and introduces and discusses an optimization design parameter which allows a cost decrease and industrial reliability improvement.

Roberto Cipollone; Andrea Cinocca; Angelo Gualtieri

2013-01-01T23:59:59.000Z

184

Process for removing metals from water  

DOE Patents (OSTI)

A process for removing metals from water including the steps of prefiltering solids from the water, adjusting the pH to between about 2 and 3, reducing the amount of dissolved oxygen in the water, increasing the pH to between about 6 and 8, adding water-soluble sulfide to precipitate insoluble sulfide- and hydroxide-forming metals, adding a containing floc, and postfiltering the resultant solution. The postfiltered solution may optionally be eluted through an ion exchange resin to remove residual metal ions. 2 tabs.

Napier, J.M.; Hancher, C.M.; Hackett, G.D.

1987-06-29T23:59:59.000Z

185

Nitrate removal from drinking water -- Review  

SciTech Connect

Nitrate concentrations in surface water and especially in ground water have increased in Canada, the US, Europe, and other areas of the world. This trend has raised concern because nitrates cause methemoglobiinemia in infants. Several treatment processes including ion exchange, biological denitrification, chemical denitrification, reverse osmosis, electrodialysis, and catalytic denitrification can remove nitrates from water with varying degrees of efficiency, cost, and ease of operation. Available technical data, experience, and economics indicate that ion exchange and biological denitrification are more acceptable for nitrate removal than reverse osmosis. Ion exchange is more viable for ground water while biological denitrification is the preferred alternative for surface water. This paper reviews the developments in the field of nitrate removal processes.

Kapoor, A.; Viraraghavan, T. [Univ. of Regina, Saskatchewan (Canada)

1997-04-01T23:59:59.000Z

186

Measuring non-condensable gases in steam  

SciTech Connect

In surgery, medical devices that are used should be sterilized. To obtain surface steam sterilization conditions, not only in the sterilizer chamber itself but also in the loads to be sterilized, the amount of non-condensable gases (NCGs), for instance air, should be very low. Even rather small fractions of NCGs (below 1%) seriously hamper steam penetration in porous materials or devices with hollow channels (e.g., endoscopes). A recently developed instrument which might detect the presence of residual NCGs in a reliable and reproducible way is the 3M{sup TM} Electronic Test System (ETS). In this paper, a physical model is presented that describes the behavior of this instrument. This model has been validated by experiments in which known fractions of NCGs were introduced in a sterilizer chamber in which an ETS was placed. Despite several approximations made in the model, a good agreement is found between the model predictions and the experimental results. The basic principle of the ETS, measuring the heat transfer by condensation on a cooled surface, permits a very sensitive detection of NCGs in harsh environments like water vapor at high temperatures and pressures. Our model may serve to develop adapted and optimized versions of this instrument for use outside the field of sterilization, e.g., in heat exchangers based on steam condensation.

Doornmalen, J. P. C. M. van; Kopinga, K., E-mail: k.kopinga@tue.nl [Department of Applied Physics, Eindhoven University of Technology, P.O. Box 513, 5600 MB Eindhoven (Netherlands)

2013-11-15T23:59:59.000Z

187

1 - Solubility of Atmospheric Gases in Freshwater  

Science Journals Connector (OSTI)

This chapter presents tabular information on the standard air saturation concentration (moist air at 1atm) for oxygen, nitrogen, argon, and carbon dioxide gas in terms of ?mol/kg, mg/L, and mL/L; and in terms of Bunsen coefficients L real gas/(Latm); mg real gas/(LmmHg); and mg real gas/(LkPa) for 040C and freshwater conditions. Because the mole fraction of carbon dioxide in the atmosphere is changing, solubility information is provided for 2010 (390?atm) and for 2030 (440?atm) based on projected atmospheric values. Tabular information is also provided to allow computation of standard air saturation concentrations of carbon dioxide gas directly as a function of atmospheric mole fraction. Conversion factors are presented to convert these concentrations to other commonly used units. Equations and tabular information are provided to compute air saturation concentration for moist air at local barometric pressure for the four atmospheric gases. Because of the importance of dissolved oxygen in biological processes, the air solubility concentration is also presented as a function of elevation for both metric and English elevations. Equations and tabular information are provided to allow conversion of concentrations in mg/L to partial pressures in mmHg. Sample problems are included for representative examples. Keywords gas solubility, freshwater, oxygen, nitrogen, argon, carbon dioxide, standard air solubility, air solubility, Bunsen coefficients, partial pressures

John Colt

2012-01-01T23:59:59.000Z

188

Photoactivated metal removal  

SciTech Connect

The authors propose the use of photochromic dyes as light activated switches to bind and release metal ions. This process, which can be driven by solar energy, can be used in environmental and industrial processes to remove metals from organic and aqueous solutions. Because the metals can be released from the ligands when irradiated with visible light, regeneration of the ligands and concentration of the metals may be easier than with conventional ion exchange resins. Thus, the process has the potential to be less expensive than currently used metal extraction techniques. In this paper, the authors report on their studies of the metal binding of spirogyran dyes and the hydrolytic stability of these dyes. They have prepared a number of spirogyrans and measured their binding constants for calcium and magnesium. They discuss the relationship of the structure of the dyes to their binding strengths. These studies are necessary towards determining the viability of this technique.

Nimlos, M.R.; Filley, J.; Ibrahim, M.A.; Watt, A.S.; Blake, D.M.

1999-07-01T23:59:59.000Z

189

Energy Efficiency and Greenhouse Gases | Department of Energy  

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

Energy Efficiency Energy Efficiency and Greenhouse Gases Energy Efficiency and Greenhouse Gases Mission The team establishes an energy conservation program as defined in Executive Order (EO) 13423, Strengthening Federal Environmental, Energy, and Transportation Management, and (EO) 13514, Federal Leadership in Environmental, Energy, and Economic Performance, and DOE Order 436.1, Departmental Sustainability, and approved by LM. The team incorporates requirements for energy efficiency and reductions in greenhouse gases, and it advocates conserving environmental resources and improving operational capabilities and mission sustainability. Scope The team evaluates how to maintain and operate its buildings and facilities in a resource-efficient, sustainable, and economically viable manner. The

190

Unified Theory of Lattice Boltzmann Models for Nonideal Gases  

SciTech Connect

A nonideal gas lattice Boltzmann model is directly derived, in an {ital a priori} fashion, from the Enskog equation for dense gases. The model is rigorously obtained by a systematic procedure to discretize the Enskog equation (in the presence of an external force) in both phase space and time. The lattice Boltzmann model derived here is thermodynamically consistent and is free of the defects which exist in previous lattice Boltzmann models for nonideal gases. The existing lattice Boltzmann models for nonideal gases are analyzed and compared with the model derived here. {copyright} {ital 1998} {ital The American Physical Society}

Luo, L. [ICASE, MS 403, NASA Langley Research Center, 6 North Dryden Street, Building 1298, Hampton, Virginia 23681-0001 (United States)] [ICASE, MS 403, NASA Langley Research Center, 6 North Dryden Street, Building 1298, Hampton, Virginia 23681-0001 (United States)

1998-08-01T23:59:59.000Z

191

Global warming description using Daisyworld model with greenhouse gases  

Science Journals Connector (OSTI)

Abstract Daisyworld is an archetypal model of the earth that is able to describe the global regulation that can emerge from the interaction between life and environment. This article proposes a model based on the original Daisyworld considering greenhouse gases emission and absorption, allowing the description of the global warming phenomenon. Global and local analyses are discussed evaluating the influence of greenhouse gases in the planet dynamics. Numerical simulations are carried out showing the general qualitative behavior of the Daisyworld for different scenarios that includes solar luminosity variations and greenhouse gases effect. Nonlinear dynamics perspective is of concern discussing a way that helps the comprehension of the global warming phenomenon.

Susana L.D. Paiva; Marcelo A. Savi; Flavio M. Viola; Albino J.K. Leiroz

2014-01-01T23:59:59.000Z

192

Ozone removal by HVAC filters  

Science Journals Connector (OSTI)

Residential and commercial HVAC filters that have been loaded with particles during operation in the field can remove ozone from intake or recirculated air. However, knowledge of the relative importance of HVAC filters as a removal mechanism for ozone in residential and commercial buildings is incomplete. We measured the ozone removal efficiencies of clean (unused) fiberglass, clean synthetic filters, and field-loaded residential and commercial filters in a controlled laboratory setting. For most filters, the ozone removal efficiency declined rapidly but converged to a non-zero (steady-state) value. This steady-state ozone removal efficiency varied from 0% to 9% for clean filters. The mean steady-state ozone removal efficiencies for loaded residential and commercial filters were 10% and 41%, respectively. Repeated exposure of filters to ozone following a 24-h period of no exposure led to a regeneration of ozone removal efficiency. Based on a theoretical scaling analysis of mechanisms that are involved in the ozone removal process, we speculate that the steady-state ozone removal efficiency is limited by reactant diffusion out of particles, and that regeneration is due to internal diffusion of reactive species to sites available to ozone for reaction. Finally, by applying our results to a screening model for typical residential and commercial buildings, HVAC filters were estimated to contribute 22% and 95%, respectively, of total ozone removal in HVAC systems.

P. Zhao; J.A. Siegel; R.L. Corsi

2007-01-01T23:59:59.000Z

193

Analysis of air pollution and greenhouse gases  

SciTech Connect

The current objective of the project Analysis of Air Pollution and Greenhouse Gases'' is to develop a study of emissions and emission sources that could easily be linked to models of economic activity. Initial studies were conducted to evaluate data currently available linking activity rates and emissions estimates. The emissions inventory developed for the National Acid Precipitation Assessment Program (NAPAP) presents one of the most comprehensive data sets, and was chosen for our initial studies, which are described in this report. Over 99% of the SO{sub 2} emissions, 98% of the NO{sub x} emission and 57% of the VOC emissions from area sources are related to fuel combustion. The majority of emission from these sources are generated by the transportation sector. Activity rates for area sources are not archived with the NAPAP inventory; alternative derivations of these data will be part of the future activities of this project. The availability and completeness of the fuel heat content data in the NAPAP inventory were also studied. Approximately 10% of the SO{sub 2} emissions, 13% of the NO{sub x} emissions and 46% of the VOC emissions are generated by sources with unavailable data for fuel heat content. Initial estimates of pollutant emission rate per unit fuel heat content. Initial estimates of pollutant emission rate per unit fuel heat content were generated. Future studies for this project include the derivation of activity rates for area sources, improved explanations for the default fuel parameters defined in the NAPAP inventory and the development of links to data bases of economic activity.

Benkovitz, C.M.

1992-03-01T23:59:59.000Z

194

Nuclear magnetic resonance of laser-polarized noble gases in molecules, materials and organisms  

SciTech Connect

Conventional nuclear magnetic resonance (NMR) spectroscopy and magnetic resonance imaging (MRI) are fundamentally challenged by the insensitivity that stems from the ordinarily low spin polarization achievable in even the strongest NMR magnets. However, by transferring angular momentum from laser light to electronic and nuclear spins, optical pumping methods can increase the nuclear spin polarization of noble gases by several orders of magnitude, thereby greatly enhancing their NMR sensitivity. This dissertation is primarily concerned with the principles and practice of optically pumped nuclear magnetic resonance (OPNMR). The enormous sensitivity enhancement afforded by optical pumping noble gases can be exploited to permit a variety of novel NMR experiments across many disciplines. Many such experiments are reviewed, including the void-space imaging of organisms and materials, NMR and MRI of living tissues, probing structure and dynamics of molecules in solution and on surfaces, and zero-field NMR and MRI.

Goodson, Boyd M.

1999-12-01T23:59:59.000Z

195

Global Research Alliance on Agricultural Greenhouse Gases | Open Energy  

Open Energy Info (EERE)

Global Research Alliance on Agricultural Greenhouse Gases Global Research Alliance on Agricultural Greenhouse Gases Jump to: navigation, search Name Global Research Alliance on Agricultural Greenhouse Gases Agency/Company /Organization United States Department of Agriculture Sector Land Focus Area Agriculture Topics GHG inventory, Policies/deployment programs Resource Type Guide/manual, Lessons learned/best practices Website http://globalresearchalliance. References Global Research Alliance on Agricultural Greenhouse Gases [1] Background "The Alliance is a bottom-up network, founded on the voluntary, collaborative efforts of countries. It will coordinate research on agricultural greenhouse gas emission reductions by linking up existing and new research efforts across a range of sub-sectors and work areas. It will

196

Method of producing pyrolysis gases from carbon-containing materials  

DOE Patents (OSTI)

A gasification process of improved efficiency is disclosed. A dual bed reactor system is used in which carbon-containing feedstock materials are first treated in a gasification reactor to form pyrolysis gases. The pyrolysis gases are then directed into a catalytic reactor for the destruction of residual tars/oils in the gases. Temperatures are maintained within the catalytic reactor at a level sufficient to crack the tars/oils in the gases, while avoiding thermal breakdown of the catalysts. In order to minimize problems associated with the deposition of carbon-containing materials on the catalysts during cracking, a gaseous oxidizing agent preferably consisting of air, oxygen, steam, and/or mixtures thereof is introduced into the catalytic reactor at a high flow rate in a direction perpendicular to the longitudinal axis of the reactor. This oxidizes any carbon deposits on the catalysts, which would normally cause catalyst deactivation.

Mudge, Lyle K. (Richland, WA); Brown, Michael D. (West Richland, WA); Wilcox, Wayne A. (Kennewick, WA); Baker, Eddie G. (Richland, WA)

1989-01-01T23:59:59.000Z

197

Spontaneous detonation of a mixture of two odd electron gases  

Science Journals Connector (OSTI)

Spontaneous detonation of a mixture of two odd electron gases ... Instructions for safe detonation of ClO2 and NO (the fastest known reaction between two stable molecules at room temperature). ...

Thomas S. Briggs

1991-01-01T23:59:59.000Z

198

Suitability of Non-Energy Greenhouse Gases for Emissions Trading  

Science Journals Connector (OSTI)

This paper assesses the suitability of different sources of non-energy greenhouse gases for emissions trading. Different forms of emissions trading are defined and criteria for determining whether a source is sui...

Erik Haites; Angelo Proestos

2000-01-01T23:59:59.000Z

199

Studying coherence in ultra-cold atomic gases  

E-Print Network (OSTI)

This thesis will discuss the study of coherence properties of ultra-cold atomic gases. The atomic systems investigated include a thermal cloud of atoms, a Bose-Einstein condensate and a fermion pair condensate. In each ...

Miller, Daniel E. (Daniel Edward)

2007-01-01T23:59:59.000Z

200

Removing Arsenic from Drinking Water  

ScienceCinema (OSTI)

See how INL scientists are using nanotechnology to remove arsenic from drinking water. For more INL research, visit http://www.facebook.com/idahonationallaboratory

None

2013-05-28T23:59:59.000Z

Note: This page contains sample records for the topic "gases removed increased" 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

Removing Arsenic from Drinking Water  

SciTech Connect

See how INL scientists are using nanotechnology to remove arsenic from drinking water. For more INL research, visit http://www.facebook.com/idahonationallaboratory

None

2011-01-01T23:59:59.000Z

202

Unsupervised One-Class Learning for Automatic Outlier Removal  

Science Journals Connector (OSTI)

Outliers are pervasive in many computer vision and pattern recognition problems. Automatically eliminating outliers scattering among practical data collections becomes increasingly important, especially for Internet inspired vision applications. In this ... Keywords: One-Class Learning, Outlier Removal

Wei Liu, Gang Hua, John R. Smith

2014-06-01T23:59:59.000Z

203

Effect of bed medium moisture on {alpha}-pinene removal by biofilters  

SciTech Connect

In this study, laboratory scale continuous flow bioifilters were used to determine the effect of bed medium moisture on biofilter performance when treating off-gases containing {alpha}-pinene. Biofilters were packed using a proprietary wood waste bed medium and were operated at a flow rate of 700 ml of air per min, yielding an empty bed residence time of 2 minutes. For the bed medium moisture levels tested, a biofilter bed held at 100% moisture on a dry weight basis demonstrated the best overall {alpha}-pinene removal results. Volumetric productivity and percent removal were higher, while the time to reach maximum removal efficiency was decreased compared to biofilters operated at 40, 60 and 80% bed medium moisture. Results indicate that control of moisture in a biofilter is important for maximum removal of {alpha}-pinene.

Lee, B.D.; Apel, W.A.; Cook, L.L. [Lockheed Martin Idaho Technologies Co., Idaho Falls, ID (United States); Nichols, K.M. [Weyerhaeuser, Federal Way, WA (United States)

1996-12-31T23:59:59.000Z

204

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

205

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

DOE Patents (OSTI)

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

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

1983-01-01T23:59:59.000Z

206

Carbonaceous material for production of hydrogen from low heating value fuel gases  

DOE Patents (OSTI)

A process for the catalytic production of hydrogen, from a wide variety of low heating value fuel gases containing carbon monoxide, comprises circulating a carbonaceous material between two reactors--a carbon deposition reactor and a steaming reactor. In the carbon deposition reactor, carbon monoxide is removed from a fuel gas and is deposited on the carbonaceous material as an active carbon. In the steaming reactor, the reactive carbon reacts with steam to give hydrogen and carbon dioxide. The carbonaceous material contains a metal component comprising from about 75% to about 95% cobalt, from about 5% to about 15% iron, and up to about 10% chromium, and is effective in suppressing the production of methane in the steaming reactor.

Koutsoukos, Elias P. (Los Angeles, CA)

1989-01-01T23:59:59.000Z

207

Energy loss characteristics of heavy ions in nitrogen, carbon dioxide, argon, hydrocarbon gases and tradescantia tissue  

E-Print Network (OSTI)

Energy loss characteristics of heavy ions in nitrogen, carbon dioxide, argon, hydrocarbon gases and tradescantia tissue

Dennis, J A

1971-01-01T23:59:59.000Z

208

Efficiency and emissions of a spark ignition engine fueled with synthetic gases obtained from catalytic decomposition of biogas  

Science Journals Connector (OSTI)

This paper presents the results of the tests developed in a naturally aspirated spark ignition engine, intended for installation in vehicles, fueled with synthetic gases obtained from catalytic decomposition of biogas. The experimental tests were carried out at three equivalence ratios and different speeds and loads. Two synthetic blends were used and the results were compared with those of gasoline and methane. Efficiency and emissions were calculated for the different fuels under the same operation conditions and it was found that at lean equivalence ratios, brake thermal efficiency with synthetic gases approached to the traditional fuels and even improved it at ?=0.7. BSCO2 emissions increased due to the CO2 content of the gaseous blends. While CO increased at stoichiometric conditions, it decreased at lean conditions because the H2 contained in synthetic gases improved combustion at these conditions. BSHC measured were very low with synthetic gases because of the low content of methane in blends. The change in the fraction of H2 and CO2 of the synthetic blends led to quite different results in BSNOx. Syngas 1 \\{BSNOx\\} emissions were the lowest of all fuels, while syngas 2 \\{BSNOx\\} were the highest because of its high H2 fraction.

J. Arroyo; F. Moreno; M. Muoz; C. Monn

2013-01-01T23:59:59.000Z

209

Finalize Historic National Program to Reduce Greenhouse Gases and Improve  

Open Energy Info (EERE)

Finalize Historic National Program to Reduce Greenhouse Gases and Improve Finalize Historic National Program to Reduce Greenhouse Gases and Improve Fuel Economy for Cars and Trucks Jump to: navigation, search Tool Summary LAUNCH TOOL Name: Finalize Historic National Program to Reduce Greenhouse Gases and Improve Fuel Economy for Cars and Trucks Agency/Company /Organization: EPA and NHTSA Focus Area: Standards - Incentives - Policies - Regulations Topics: Policy Impacts Resource Type: Reports, Journal Articles, & Tools Website: www.epa.gov/oms/climate/regulations/420f10014.pdf This document establish a national program consisting of new standards for model year 2012 through 2016 light-duty vehicles that will reduce greenhouse gas emissions and improve fuel economy. EPA is finalizing the first-ever national greenhouse gas (GHG) emissions standards under the

210

Voluntary Reporting of Greenhouse Gases Program - Electricity Factors  

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

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

211

Greenhouse Gases, Regulated Emissions, and Energy Use in Transportation  

Open Energy Info (EERE)

Greenhouse Gases, Regulated Emissions, and Energy Use in Transportation Greenhouse Gases, Regulated Emissions, and Energy Use in Transportation (GREET) Model Jump to: navigation, search Tool Summary LAUNCH TOOL Name: Greenhouse Gases, Regulated Emissions, and Energy Use in Transportation (GREET) Model Agency/Company /Organization: Argonne National Laboratory Focus Area: GHG Inventory Development Topics: Analysis Tools Website: greet.es.anl.gov/ This full life-cycle model evaluates the energy and emission impacts of advanced vehicle technologies and new transportation fuels. The model allows users to evaluate various vehicle and fuel combinations. How to Use This Tool This tool is most helpful when using these strategies: Shift - Change to low-carbon modes Improve - Enhance infrastructure & policies Learn more about the avoid, shift, improve framework for limiting air

212

Lattice vibrations of pure and doped GaSe  

SciTech Connect

The Bridgman method is used to grow especially undoped and doped single crystals of GaSe. Composition and impurity content of the grown crystals were determined using X-ray fluorescence (XRF) method. X-ray diffraction, Raman scattering, photoluminescence (PL), and IR transmission measurements were performed at room temperature. The long wavelength lattice vibrations of four modifications of GaSe were described in the framework of modified one-layer linear-chain model which also takes into consideration the interaction of the selenium (Se) atom with the second nearest neighbor gallium (Ga) atom in the same layer. The existence of an eight-layer modification of GaSe is suggested and the vibrational frequencies of this modification are explained in the framework of a lattice dynamical model considered in the present work. Frequencies and the type of vibrations (gap, local, or resonance) for the impurity atoms were calculated and compared with the experimental results.

Allakhverdiev, K. [Materials Institute, Marmara Research Center, TUBITAK, Gebze/Kocaeli 41470 (Turkey) and Institute of Physics, Azerbaijan National Academy of Sciences, Baku AZ1143 (Azerbaijan)]. E-mail: kerim.allahverdi@mam.gov.tr; Baykara, T. [Materials Institute, Marmara Research Center, TUBITAK, Gebze/Kocaeli 41470 (Turkey); Ellialtioglu, S. [Department of Physics, Middle East Technical University, Ankara 06531 (Turkey); Hashimzade, F. [Institute of Physics, Azerbaijan National Academy of Sciences, Baku AZ1143 (Azerbaijan); Huseinova, D. [Institute of Physics, Azerbaijan National Academy of Sciences, Baku AZ1143 (Azerbaijan); Kawamura, K. [Institute of Materials Science, University of Tsukuba 305-8573 (Japan); Kaya, A.A. [Materials Institute, Marmara Research Center, TUBITAK, Gebze/Kocaeli 41470 (Turkey); Kulibekov, A.M. [Department of Physics, Mugla University, Mugla 48000 (Turkey); Onari, S. [Institute of Materials Science, University of Tsukuba 305-8573 (Japan)

2006-04-13T23:59:59.000Z

213

Emissions of greenhouse gases in the United States 1997  

SciTech Connect

This is the sixth annual report on aggregate US national emissions of greenhouse gases. It covers emissions over the period 1990--1996, with preliminary estimates of emissions for 1997. Chapter one summarizes some background information about global climate change and the greenhouse effect. Important recent developments in global climate change activities are discussed, especially the third Conference of the Parties to the Framework Convention on Climate Change, which was held in December of 1997 in Kyoto, Japan. Chapters two through five cover emissions of carbon dioxide, methane, nitrous oxide, halocarbons and related gases, respectively. Chapter six describes potential sequestration and emissions of greenhouse gases as a result of land use changes. Six appendices are included in the report. 96 refs., 38 tabs.

NONE

1998-10-01T23:59:59.000Z

214

Assess Potential Agency Size Changes to Reduce Greenhouse Gases Using  

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

Assess Potential Agency Size Changes to Reduce Greenhouse Gases Assess Potential Agency Size Changes to Reduce Greenhouse Gases Using Renewable Energy in Buildings Assess Potential Agency Size Changes to Reduce Greenhouse Gases Using Renewable Energy in Buildings October 7, 2013 - 11:15am Addthis To support planning for using renewable energy to reduce greenhouse gas (GHG) emissions at the Federal agency or program-level, it is important to consider what changes to the agencies building or land-holding portfolio may have on opportunities for renewable energy. Changes to consider include: Addition of new buildings or sites to the agencies portfolio Major renovations to existing buildings Office moves into or out of agency-owned or leased space. As is the case with planning energy efficiency measures, planning for renewable energy in new construction can be more cost-effective than

215

Raman/FTIR spectroscopy of oil shale retort gases  

SciTech Connect

A Raman facility was assembled in order to aid in the evaluation of the feasibility of using Raman or FTIR spectroscopy for analyzing gas mixtures of interest in oil shale. Applications considered in oil shale research included both retort monitoring and laboratory kinetic studies. Both techniques gave limits of detection between 10 and 1000 ppM for ten representative pertinent gases. Both techniques are inferior as a general analytical technique for oil shale gas analysis in comparison with mass spectroscopy, which had detection limits between 1 and 50 ppM for the same gases. The conclusion of the feasibility study was to recommend that mass spectroscopic techniques be used for analyzing gases of interest to oil shale.

Richardson, J H; Monaco, S B; Sanborn, R H; Hirschfeld, T B; Taylor, J R

1982-08-01T23:59:59.000Z

216

Bacterially mediated removal of phosphorus and cycling of nitrate and sulfate in the waste stream  

E-Print Network (OSTI)

with an increase in ammonia showing there had to be an additional P removal process at the same timeBacterially mediated removal of phosphorus and cycling of nitrate and sulfate in the waste stream sludge Phosphorus removal Denitrification Apatite formation Sulfur cycling a b s t r a c t Simultaneous

Benning, Liane G.

217

Effect of Xylan and Lignin Removal by Batch and Flowthrough Pretreatment  

E-Print Network (OSTI)

Effect of Xylan and Lignin Removal by Batch and Flowthrough Pretreatment on the Enzymatic understand these trade-offs, comparative data are reported on xylan and lignin removal and enzymatic with just water enhanced the xylan dissolution rate, more than doubled total lignin removal, and increased

California at Riverside, University of

218

WCH Removes Massive Test Reactor  

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

RICHLAND, WA -- Hanford's River Corridor contractor, Washington Closure Hanford, has met a significant cleanup challenge on the U.S. Department of Energy's (DOE) Hanford Site by removing a 1,082...

219

Pileup Removal Algorithms  

E-Print Network (OSTI)

One of the main challenges of the upcoming LHC run will be the increase of instantaneous luminosity, which will result in a large number of additional proton-proton collisions in each event (pileup). In such a high pileup environment, the accurate reconstruction of jet properties and shapes will be more and more demanding. In this note, the performances of various advanced pileup mitigation tools such as charged hadron subtraction, grooming techniques, jet cleansing and per particle pileup approaches are studied. The focus is on preparation for LHC Run II for which we expect up to 40 additional pileup events on average and includes comparisons to LHC Run I data which has typically 20 additional pileup events on average.

CMS Collaboration

2014-01-01T23:59:59.000Z

220

Hazardous Gases VASILIS M. FTHENAKIS Department of Applied Science  

Office of Scientific and Technical Information (OSTI)

Mitigation Options for Mitigation Options for Accidental Releases of Hazardous Gases VASILIS M. FTHENAKIS Department of Applied Science Brookhaven National Laboratory Upton, N Y 11973 ABSTRACT The objective of this paper is to review and compare technologies available for mitigation of unconfined releases of toxic and flammable gases. These technologies indude: secondary confinement, de- inventory, vapor barriers, foam spraying, and water sprays/monitors. Guidelines for the design and/or operation of effective post-release mitigation systems and case studies involving actual industrial mitigation systems are also presented. 1. ACCIDENT PREVENTION & MITIGATION OPTIONS Accident prevention and mitigation in the process industries is based on the military concept of defense in

Note: This page contains sample records for the topic "gases removed increased" 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

Dissipative dynamics of a Josephson junction in the Bose gases  

SciTech Connect

The dissipative dynamics of a Josephson junction in Bose gases is considered within the framework of the model of a tunneling Hamiltonian. The effective action that describes the dynamics of the phase difference across the junction is derived using the functional integration method. The dynamic equation obtained for the phase difference across the junction is analyzed for the finite temperatures in the low-frequency limit involving the radiation terms. The asymmetric case of the Bose gases with the different order parameters is calculated as well.

Barankov, R.A. [Department of Physics, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139 (United States); Burmistrov, S.N. [RRC 'Kurchatov Institute', Kurchatov Sq.1, 123182 Moscow (Russian Federation)

2003-01-01T23:59:59.000Z

222

Critical behavior of two freely evolving granular gases separated by an adiabatic piston  

E-Print Network (OSTI)

Two granular gases separated by an adiabatic piston and initially in the same macroscopic state are considered. It is found that a phase transition with an spontaneous symmetry breaking occurs. When the mass of the piston is increased beyond a critical value, the piston moves to a stationary position different from the middle of the system. The transition is accurately described by a simple kinetic model that takes into account the velocity fluctuations of the piston. Interestingly, the final state is not characterized by the equality of the temperatures of the subsystems but by the cooling rates being the same. Some relevant consequences of this feature are discussed.

J. Javier Brey; Nagi Khalil

2010-09-23T23:59:59.000Z

223

Polycyclic aromatic hydrocarbon emission profiles and removal efficiency by electrostatic precipitator and wetfine scrubber in an iron ore sintering plant  

SciTech Connect

A monitoring campaign of polychlorinated dibenzo-p-dioxins and dibenzofurans, polyaromatic hydrocarbons (PAHs), and polychlorinated biphenyl was carried out in an Italian iron ore sintering plant by sampling the combustion gases at the electrostatic precipitator (ESP) outlet, at the Wetfine scrubber (WS) outlet, and by collecting the ESP dust. Few data are available on these micropollutants produced in iron ore sintering plants, particularly from Italian plants. This study investigates the PAH emission profiles and the removal efficiency of ESPs and WS. PAHs were determined at the stack, ESP outlet flue gases, and in ESP dust to characterize the emission profiles and the performance of the ESP and the WS for reducing PAH emission. The 11 PAHs monitored are listed in the Italian legislative decree 152/2006. The mean total PAH sum concentration in the stack flue gases is 3.96 {mu}g/N m{sup 3}, in ESP outlet flue gases is 9.73 {mu}g/N m{sup 3}, and in ESP dust is 0.53 {mu}g/g. Regarding the emission profiles, the most abundant compound is benzo(b)fluoranthene, which has a relative low BaP toxic equivalency factors (TEF) value, followed by dibenzo(a,l)pyrene, which has a very high BaP(TEF) value. The emission profiles in ESP dust and in the flue gases after the ESP show some changes, whereas the fingerprint in ESP and stack flue gases is very similar. The removal efficiency of the ESP and of WS on the total PAH concentration is 5.2 and 59.5%, respectively. 2 figs., 5 tabs.

Ettore Guerriero; Antonina Lutri; Rosanna Mabilia; Maria Concetta Tomasi Sciano; Mauro Rotatori [Istituto sull'Inquinamento Atmosferico, Monterotondo Scalo (Italy). Consiglio Nazionale delle Ricerche

2008-11-15T23:59:59.000Z

224

AER1301: KINETIC THEORY OF GASES Assignment #2  

E-Print Network (OSTI)

AER1301: KINETIC THEORY OF GASES Assignment #2 1. Using the formalism of the text book is as follows. Assume that the particle number density is a slowly varying function of the z coordinate #27; ? is a constant. 3. Show that if the potential function, U(r), varies as 1=r 4

Groth, Clinton P. T.

225

AER1301: KINETIC THEORY OF GASES Assignment #2  

E-Print Network (OSTI)

AER1301: KINETIC THEORY OF GASES Assignment #2 1. Using the formalism of the text book the particle number density and temperature are both slowly varying functions of the z coordinate of the previous problem is as follows. Assume that the particle number density is a slowly varying function

Groth, Clinton P. T.

226

OPTIONS FOR ABATING GREENHOUSE GASES FROM EXHAUST STREAMS.  

SciTech Connect

This report examines different alternatives for replacing, treating, and recycling greenhouse gases. It is concluded that treatment (abatement) is the only viable short-term option. Three options for abatement that were tested for use in semiconductor facilities are reviewed, and their performance and costs compared. This study shows that effective abatement options are available to the photovoltaic (PV) industry, at reasonable cost.

FTHENAKIS,V.

2001-12-01T23:59:59.000Z

227

Automatic Process Chromatographs for the Analysis of Corrosive Fluoride Gases  

Science Journals Connector (OSTI)

......hexaflu- oride matrix gas by a trapping procedure...the disadvantage of high cost and require skilled and...lacked reliability in gases of high halocarbon coolant...the uranium hexafluoride gas; impurities have a direct effect on production efficiency. Coolant-114......

J. G. Million; W. S. Pappas; C. W. Weber

1969-03-01T23:59:59.000Z

228

Optical Third-Harmonic Coefficients for Inert Gases  

Science Journals Connector (OSTI)

Optical third-harmonic coefficients ?zzzz(3?) for the inert gases have been calculated taking the LS coupling scheme for helium and Jj and jl coupling schemes for neon, argon, and krypton. Our calculated values agree reasonably well with the experimental values of set (i) of Ward and New.

B. P. Tripathi; R. K. Laloraya; S. L. Srivastava

1971-11-01T23:59:59.000Z

229

Mitigation options for accidental releases of hazardous gases  

SciTech Connect

The objective of this paper is to review and compare technologies available for mitigation of unconfined releases of toxic and flammable gases. These technologies include: secondary confinement, deinventory, vapor barriers, foam spraying, and water sprays/monitors. Guidelines for the design and/or operation of effective post-release mitigation systems and case studies involving actual industrial mitigation systems are also presented.

Fthenakis, V.M.

1995-05-01T23:59:59.000Z

230

SAFT Modeling of the Solubility of Gases in Perfluoroalkanes  

Science Journals Connector (OSTI)

SAFT Modeling of the Solubility of Gases in Perfluoroalkanes ... A molecular model within a SAFT context for quantitatively predicting the solubility of xenon and oxygen in n-perfluoroalkanes is presented and discussed here. ... Free-Volume Theory Coupled with Soft-SAFT for Viscosity Calculations: Comparison with Molecular Simulation and Experimental Data ...

Ana M. A. Dias; Josep C. Pmies; Joo A. P. Coutinho; Isabel M. Marrucho; Lourdes F. Vega

2003-12-30T23:59:59.000Z

231

Recommendation 199: Recommendation to Remove Uncontaminated Areas...  

Office of Environmental Management (EM)

9: Recommendation to Remove Uncontaminated Areas of the Oak Ridge Reservation from the National Priorities List Recommendation 199: Recommendation to Remove Uncontaminated Areas of...

232

Perdido LF-Gase to Electricity  

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

E E S S O N S L E A R N E D : C H A L L E N G E S A N D S U C C E S S E S Perdido LF-Gas to Electricity Escambia County, Florida Background  Perdido LF Gas-to-Energy Project (1997-2008)  Direct Use by Paper Mill (IP)  LFG piped from Perdido Landfill to IP Direct Use of LFG  Landfill Gas fueled IP boiler  Project developed and managed by 3 rd party vendor  Vendor managed the gas wellfield  County received minimum compensation from vendor for Gas Rights  Vendor received compensation from IP for fuel used Project Issues  Demand for LFG at IP for fuel fell off  LFG compliance at Perdido LF not a priority for vendor  Surface and boundary emissions increased  Vendor reluctant to implement additional control measures  Contract grey areas Rebirth of LFG Beneficial Reuse

233

SYNTHESIS AND CHARACTERIZATION OF NANO-STRUCTURED CHELATING ADSORBENTS FOR THE DIRECT REMOVAL OF MERCURY VAPOR FROM FLUE-GASES.  

E-Print Network (OSTI)

??Coal-Fired utility boilers are currently the largest single-known source of anthropogenic mercury emissions in the United States. In this research, the potential of gas-phase chelating (more)

ABU-DAABES, MALYUBA ALI

2005-01-01T23:59:59.000Z

234

Methods and sorbents for utilizing a hot-side electrostatic precipitator for removal of mercury from combustion gases  

DOE Patents (OSTI)

Methods are provided for reducing emission of mercury from a gas stream by treating the gas with carbonaceous mercury sorbent particles to reduce the mercury content of the gas; collecting the carbonaceous mercury sorbent particles on collection plates of a hot-side ESP; periodically rapping the collection plates to release a substantial portion of the collected carbonaceous mercury sorbent particles into hoppers; and periodically emptying the hoppers, wherein such rapping and emptying are done at rates such that less than 70% of mercury adsorbed onto the mercury sorbent desorbs from the collected mercury sorbent into the gas stream.

Nelson, Sidney (Hudson, OH)

2011-02-15T23:59:59.000Z

235

Removing Stains from Washable Fabrics.  

E-Print Network (OSTI)

of May 8, 1914, as amended, and June 30, 1914, in cooperation with the United States Department of Agriculture. Zerle L. Carpenter, Director, Texas Agricultural Extension Service, The Texas A&M University System. lOM-1l-88, New CLO ...I UUL. Z TA24S.7 8873 NO.1616 B.1616 / Texas Agricultural Extension Service LIBRARY FEB 0 1 1989 Texas A&M University Removing Stains from Washable Fabrics Ann Vanderpoorten 8eard* Most spots and stains can be removed by prompt...

Beard, Ann Vanderpoorten

1988-01-01T23:59:59.000Z

236

Strongly interacting Fermi gases : non-equilibrium dynamics and dimensional crossover  

E-Print Network (OSTI)

Experiments using ultracold atomic gases address fundamental problems in many-body physics. This thesis describes experiments on strongly-interacting gases of fermionic atoms, with a focus on non-equilibrium physics and ...

Sommer, Ariel T. (Ariel Tjodolv)

2013-01-01T23:59:59.000Z

237

Heat Transfer at Low Temperatures between Tube Walls and Gases in Turbulent Flow  

Science Journals Connector (OSTI)

...September 1947 research-article Heat Transfer at Low Temperatures between Tube...counter-flow system to study heat transfer between tube walls and gases at...Determinations on friction accompanying heat transfer with gases in turbulent flow at...

1947-01-01T23:59:59.000Z

238

Greenhouse Gases (GHG) Emissions from Gas Field Water in Southern Gas Field, Sichuan Basin, China  

Science Journals Connector (OSTI)

In order to assess correctly the gases emissions from oil/gas field water and its contributions to the source of greenhouse gases (GHG) at the atmospheric temperature and pressure, ... first developed to study th...

Guojun Chen; Wei Yang; Xuan Fang; Jiaai Zhong

2014-03-01T23:59:59.000Z

239

Simultaneous Gas Chromatographic Determination of Four Toxic Gases Generally Present in Combustion Atmospheres  

Science Journals Connector (OSTI)

......determining these gases in mixtures...dioxide, nitrogen, water vapor, and...determining these gases in mixtures...dioxide, nitrogen, water vapor, and...to the solubility of A HCN in water, which was...thevariationin gas con- centrations......

Boyd R. Endecott; Donald C. Sanders; Arvind K. Chaturvedi

1996-01-01T23:59:59.000Z

240

E-Print Network 3.0 - atmospheric gases final Sample Search Results  

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

on Climate and Planets http:icp.giss.nasa.gov The Role of the Atmosphere and Greenhouse Effect in Summary: gases, and scenario 3 - an atmosphere and greenhouse gases. Use...

Note: This page contains sample records for the topic "gases removed increased" 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

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

242

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

243

System for trapping and storing gases for subsequent chemical reduction to solids  

DOE Patents (OSTI)

A system for quantitatively reducing oxide gases. A pre-selected amount of zinc is provided in a vial. A tube is provided in the vial. The zinc and the tube are separated. A pre-selected amount of a catalyst is provided in the tube. Oxide gases are injected into the vial. The vial, tube, zinc, catalyst, and the oxide gases are cryogenically cooled. At least a portion of the vial, tube, zinc, catalyst, and oxide gases are heated.

Vogel, John S. (San Jose, CA); Ognibene, Ted J. (Oakland, CA); Bench, Graham S. (Livermore, CA); Peaslee, Graham F. (Holland, MI)

2009-11-03T23:59:59.000Z

244

E-Print Network 3.0 - atmospheric greenhouse gases Sample Search...  

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

to longwave radiation 12;Greenhouse Gases Polyatomic molecules... the greenhouse effect ... Source: Frierson, Dargan - Department of Atmospheric Sciences, University of...

245

Massive Hanford Test Reactor Removed - Plutonium Recycle Test...  

Office of Environmental Management (EM)

Massive Hanford Test Reactor Removed - Plutonium Recycle Test Reactor removed from Hanford's 300 Area Massive Hanford Test Reactor Removed - Plutonium Recycle Test Reactor removed...

246

Remote target removal for the Oak Ridge 86-inch Cyclotron  

SciTech Connect

A remotely operated target remover has been plaed in operation at the 86-Inch Cyclotron located in Oak Ridge. The system provides for the remote removal of a target from inside the cyclotron, loading it into a cask, and the removal of the cask from the 1.5 m (5-ft) shielding walls. The remote system consists of multiple electrical and pneumatically operated equipment which is designed for controlled step-by-step operation, operated with an electrical control panel, and monitored by a television system. The target remover has reduced the radiation exposures to operating personnel at the facility and has increased the effective operating time. The system is fast, requires a minimum of skill to operate, and has demonstrated both reliability and durability.

Walls, A.A.

1982-01-01T23:59:59.000Z

247

Multipollutant Removal with WOWClean System  

E-Print Network (OSTI)

such as petcoke, coal, wood, diesel and natural gas. In addition to significant removal of CO2, test results demonstrate the capability to reduce 99.5% SOx (from levels as high as 2200 ppm), 90% reduction of NOx, and > 90% heavy metals. The paper will include...

Romero, M.

2010-01-01T23:59:59.000Z

248

What are greenhouse gases? Many chemical compounds in the atmosphere act as  

E-Print Network (OSTI)

back into space. However, greenhouse gases will not let all the infrared light pass throughWhat are greenhouse gases? Many chemical compounds in the atmosphere act as greenhouse gases the land and oceans. The warmed Earth releases this heat in the form of infrared light (longwave radiation

249

Low-quality natural gas sulfur removal/recovery  

SciTech Connect

A significant fraction of U.S. natural gas reserves are subquality due to the presence of acid gases and nitrogen; 13% of existing reserves (19 trillion cubic feed) may be contaminated with hydrogen sulfide. For natural gas to be useful as fuel and feedstock, this hydrogen sulfide has to be removed to the pipeline specification of 4 ppm. The technology used to achieve these specifications has been amine, or similar chemical or physical solvent, absorption. Although mature and widely used in the gas industry, absorption processes are capital and energy-intensive and require constant supervision for proper operation. This makes these processes unsuitable for treating gas at low throughput, in remote locations, or with a high concentration of acid gases. The U.S. Department of Energy, recognizes that exploitation of smaller, more sub-quality resources will be necessary to meet demand as the large gas fields in the U.S. are depleted. In response to this need, Membrane Technology and Research, Inc. (MTR) has developed membranes and a membrane process for removing hydrogen sulfide from natural gas. During this project, high-performance polymeric thin-film composite membranes were brought from the research stage to field testing. The membranes have hydrogen sulfide/methane selectivities in the range 35 to 60, depending on the feed conditions, and have been scaled up to commercial-scale production. A large number of spiral-wound modules were manufactured, tested and optimized during this project, which culminated in a field test at a Shell facility in East Texas. The short field test showed that membrane module performance on an actual natural gas stream was close to that observed in the laboratory tests with cleaner streams. An extensive technical and economic analysis was performed to determine the best applications for the membrane process. Two areas were identified: the low-flow-rate, high-hydrogen-sulfide-content region and the high-flow-rate, high-hydrogen-sulfide-content region. In both regions the MTR membrane process will be combined with another process to provide the necessary hydrogen sulfide removal from the natural gas. In the first region the membrane process will be combined with the SulfaTreat fixed-bed absorption process, and in the second region the membrane process will be combined with a conventional absorption process. Economic analyses indicate that these hybrid processes provide 20-40% cost savings over stand-alone absorption technologies.

K. Amo; R.W. Baker; V.D. Helm; T. Hofmann; K.A. Lokhandwala; I. Pinnau; M.B. Ringer; T.T. Su; L. Toy; J.G. Wijmans

1998-01-29T23:59:59.000Z

250

Process studies for a new method of removing H/sub 2/S from industrial gas streams  

SciTech Connect

A process for the removal of hydrogen sulfide from coal-derived gas streams has been developed. The basis for the process is the absorption of H/sub 2/S into a polar organic solvent where it is reacted with dissolved sulfur dioxide to form elemental sulfur. After sulfur is crystallized from solution, the solvent is stripped to remove dissolved gases and water formed by the reaction. The SO/sub 2/ is generated by burning a portion of the sulfur in a furnace where the heat of combustion is used to generate high pressure steam. The SO/sub 2/ is absorbed into part of the lean solvent to form the solution necessary for the first step. The kinetics of the reaction between H/sub 2/S and SO/sub 2/ dissolved in mixtures of N,N-Dimethylaniline (DMA)/ Diethylene Glycol Monomethyl Ether and DMA/Triethylene Glycol Dimethyl Ether was studied by following the temperature rise in an adiabatic calorimeter. This irreversible reaction was found to be first-order in both H/sub 2/S and SO/sub 2/, with an approximates heat of reaction of 28 kcal/mole of SO/sub 2/. The sole products of the reaction appear to be elemental sulfur and water. The presence of DMA increases the value of the second-order rate constant by an order of magnitude over that obtained in the glycol ethers alone. Addition of other tertiary aromatic amines enhances the observed kinetics; heterocyclic amines (e.g., pyridine derivatives) have been found to be 10 to 100 times more effective as catalysts when compared to DMA.

Neumann, D.W.; Lynn, S.

1986-07-01T23:59:59.000Z

251

Agricultural Mitigation of Greenhouse Gases: Science and Policy Options  

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

Agricultural Mitigation of Greenhouse Gases: Science and Policy Options Agricultural Mitigation of Greenhouse Gases: Science and Policy Options Keith Paustian (keithp@nrel.colostate.edu; 970-491-1547) Natural Resource Ecology Laboratory Colorado State University Ft. Collins, CO 80523 Bruce Babcock (babcock@iastate.edu; 515-294-6785) Cathy Kling (ckling@iastate.edu; 515-294-5767) Center for Agriculture and Rural Development Iowa State University Ames, IA 50011-1070 Jerry Hatfield (hatfield@nstl.gov; 515-294-5723) USDA - National Soil Tilth Laboratory Ames, IA 50011 Rattan Lal (lal.1@osu.edu; 614-292-9069) School of Natural Resources The Ohio State University Columbus, OH 43210-1085 Bruce McCarl (mccarl@tamu.edu; 979-845-1706) Department of Agricultural Economics Texas A&M University College Station, TX 77843-2124 Sandy McLaughlin (un4@ornl.gov; 865-574-7358)

252

EIA - Emissions of Greenhouse Gases in the United States 2009  

Gasoline and Diesel Fuel Update (EIA)

Environment Environment Emissions of Greenhouse Gases in the U. S. Release Date: March 31, 2011 | Next Release Date: Report Discontinued | Report Number: DOE/EIA-0573(2009) This report-the eighteenth annual report-presents the U.S. Energy Information Administration's latest estimates of emissions for carbon dioxide, methane, nitrous oxide, and other greenhouse gases. Download the GHG Report Introduction For this report, activity data on coal and natural gas consumption and electricity sales and losses by sector were obtained from the January 2011 Monthly Energy Review (MER). In keeping with current international practice, this report presents data on greenhouse gas emissions in million metric tons carbon dioxide equivalent. The data can be converted to carbon equivalent units by

253

EIA-Voluntary Reporting of Greenhouse Gases Program - Getting Started  

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

Getting Started Getting Started Voluntary Reporting of Greenhouse Gases Program Getting Started Form EIA-1605 may seem daunting at first, even for entities that have reported under the original program. That's why EIA has developed the Getting Started page to help entities take a systematic approach to reporting their emissions and reductions. The Voluntary Reporting of Greenhouse Gases Program suggests that prospective reporters familiarize themselves with the specific requirements for reporting their entity's inventory and reductions by answering the questions embodied in the 10 steps below. In addition, EIA has prepared the interactive Getting Started tool to help reporters determine what parts of Form EIA-1605 they need to complete. Getting Started Tool Getting Started PDF Tables

254

Transporting & Shipping Hazardous Materials at LBNL: Compressed Gases  

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

Compressed Gases Compressed Gases Self-Transport by Hand & Foot Self-Transport by Vehicle Ship by Common Carrier Conduct Field Work Return Cylinders Self-Transport by Hand & Foot Staff may personally move (self-transport) compressed gas cylinders by hand & foot between buildings and in connecting spaces (i.e., hallways, elevators, etc.) within buildings provided it can be done safely. The following safety precautions apply: Use standard cylinder dollies to transport compressed gas cylinders. While dollies are preferred, cylinders weighing 11 Kg (25 lbs) or less may be hand-carried. Never move a cylinder with a regulator connected to it. Cylinder valve-protection caps and valve-opening caps must be in place when moving cylinders. Lecture bottles and other cylinders that are

255

Recovery of CO2 from Flue Gases: Commercial Trends  

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

CO CO 2 from Flue Gases: Commercial Trends Originally presented at the Canadian Society of Chemical Engineers annual meeting October 4-6, 1999, Saskatoon, Saskatchewan, Canada Authors: Dan G. Chapel (dan.chapel@fluor.com; 949-349-7530) Carl L. Mariz (carl.mariz@fluor.com; 949-349-7530) FluorDaniel One Fluor Drive Aliso Viejo CA, 92698 John Ernest (john.ernest@minimed.com; 818-576-4293) Advanced Quality Services Inc 11024 Balboa Blvd. PMB154, Granada Hills, CA 91344-5007 1 Recovery of CO 2 from Flue Gases: Commercial Trends Originally presented at the Canadian Society of Chemical Engineers annual meeting October 4-6, 1999, Saskatoon, Saskatchewan, Canada Authors: Dan Chapel - Fluor Daniel Inc., Senior Vice President Technology; Oil, Gas & Power John Ernest - Advanced Quality Services Inc., Validation Engineer

256

PPPL wins Department of Energy award for reducing greenhouse gases |  

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

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

257

Reading Comprehension - Properties of Solids, Liquids, and Gases  

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

Properties of Solids, Liquids, and Gases Properties of Solids, Liquids, and Gases A solid has a definite _________ mass texture volume and a _________ 3D irregular definite shape. The particles in a solid are _________ free to move around motionless packed tightly together . Particles in a solid move by _________ sliding past one another vibrating back and forth slightly jiggling around . _________ Viscosity Amorphous Crystalline solids soften before melting. The particles in this type of solid are not arranged in regular pattern. Amorphous solids _________ do don't have a distinct melting point. Crystalline solids have a _________ distinct color and shape distinct pattern and melting point . Liquids have no _________ volume mass shape of their own. A liquid takes the shape of its container. Without a container liquids spread into a wide,

258

PPPL Wins Department of Energy Award For Reducing Greenhouse Gases |  

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

Wins Department of Energy Award For Reducing Greenhouse Gases Wins Department of Energy Award For Reducing Greenhouse Gases By Jeanne Jackson DeVoe October 2, 2012 Tweet Widget Facebook Like Google Plus One PPPL's Tim Stevenson takes inventory of the SF6 levels at a power supply tank for NSTX. (Photo by Elle Starkman, PPPL Office of Communications) PPPL's Tim Stevenson takes inventory of the SF6 levels at a power supply tank for NSTX. The U.S. Department of Energy's (DOE) Princeton Plasma Physics Laboratory (PPPL) has received a federal Sustainability Award for reducing overall greenhouse gas emissions 48 percent since 2008 - far exceeding the U.S. government's goal of a 28 percent reduction. Members of the PPPL staff were among the 20 recipients of the Sustainability Awards in a ceremony in Washington, D.C., on Thursday, Sept.

259

The extreme nonlinear optics of gases and femtosecond optical filamentation  

SciTech Connect

Under certain conditions, powerful ultrashort laser pulses can form greatly extended, propagating filaments of concentrated high intensity in gases, leaving behind a very long trail of plasma. Such filaments can be much longer than the longitudinal scale over which a laser beam typically diverges by diffraction, with possible applications ranging from laser-guided electrical discharges to high power laser propagation in the atmosphere. Understanding in detail the microscopic processes leading to filamentation requires ultrafast measurements of the strong field nonlinear response of gas phase atoms and molecules, including absolute measurements of nonlinear laser-induced polarization and high field ionization. Such measurements enable the assessment of filamentation models and make possible the design of experiments pursuing applications. In this paper, we review filamentation in gases and some applications, and discuss results from diagnostics developed at Maryland for ultrafast measurements of laser-gas interactions.

Milchberg, H. M.; Chen, Y.-H.; Cheng, Y.-H.; Jhajj, N.; Palastro, J. P.; Rosenthal, E. W.; Varma, S.; Wahlstrand, J. K.; Zahedpour, S. [Institute for Research in Electronics and Applied Physics, University of Maryland, College Park, Maryland 20742 (United States)

2014-10-15T23:59:59.000Z

260

Apparatus for the plasma destruction of hazardous gases  

DOE Patents (OSTI)

A plasma cell for destroying hazardous gases. An electric-discharge cell having an electrically conducting electrode onto which an alternating high-voltage waveform is impressed and a dielectric barrier adjacent thereto, together forming a high-voltage electrode, generates self-terminating discharges throughout a volume formed between this electrode and a grounded conducting liquid electrode. The gas to be transformed is passed through this volume. The liquid may be flowed, generating thereby a renewable surface. Moreover, since hydrochloric and hydrofluoric acids may be formed from destruction of various chlorofluorocarbons in the presence of water, a conducting liquid may be selected which will neutralize these corrosive compounds. The gases exiting the discharge region may be further scrubbed if additional purification is required.

Kang, Michael (Los Alamos, NM)

1995-01-01T23:59:59.000Z

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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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261

Apparatus for the plasma destruction of hazardous gases  

DOE Patents (OSTI)

A plasma cell for destroying hazardous gases is described. An electric-discharge cell having an electrically conducting electrode onto which an alternating high-voltage waveform is impressed and a dielectric barrier adjacent thereto, together forming a high-voltage electrode, generates self-terminating discharges throughout a volume formed between this electrode and a grounded conducting liquid electrode. The gas to be transformed is passed through this volume. The liquid may be flowed, generating thereby a renewable surface. Moreover, since hydrochloric and hydrofluoric acids may be formed from destruction of various chlorofluorocarbons in the presence of water, a conducting liquid may be selected which will neutralize these corrosive compounds. The gases exiting the discharge region may be further scrubbed if additional purification is required. 4 figs.

Kang, M.

1995-02-07T23:59:59.000Z

262

Reduction of greenhouse gases using renewable energies in Mexico 2025  

Science Journals Connector (OSTI)

This study presents three scenarios relating to the environmental futures of Mexico up to the year 2025. The first scenario emphasizes the use of oil products, particularly fueloil, and represents the energy policy path that was in effect until 1990. The second scenario prioritizes the use of natural gas, reflecting the energy consumption pattern that arose in the mid-1990s as a result of reforms in the energy sector. In the third scenario, the high participation of renewable sources of energy, in particular renewable hydrogen, is considered feasible from a technical and economic point of view. The three scenarios are evaluated up to the year 2025 in terms of greenhouse gases (GHG), acid rain precursor gases (ARPG), and environmentenergy intensity factors.

F Manzini; J Islas; M Mart??nez

2001-01-01T23:59:59.000Z

263

Evaluacin de la generacin de gases de efecto invernadero asociados al ciclo de vida de los biocombustibles colombianos = Assessment of greenhouse gases emissions associated to colombian biofuels lifecycle.  

E-Print Network (OSTI)

??Valencia Botero, Monica Julieth (2012) Evaluacin de la generacin de gases de efecto invernadero asociados al ciclo de vida de los biocombustibles colombianos = Assessment (more)

Valencia Botero, Monica Julieth

2012-01-01T23:59:59.000Z

264

Extraction of uranium from spent fuels using liquefied gases  

SciTech Connect

For reprocessing of spent nuclear fuels, a novel method to extract actinides from spent fuel using highly compressed gases, nitrogen dioxide and carbon dioxide was proposed. As a fundamental study, the nitrate conversion with liquefied nitrogen dioxide and the nitrate extraction with supercritical carbon dioxide were demonstrated by using uranium dioxide powder, uranyl nitrate and tri-n-butylphosphate complex in the present study. (authors)

Sawada, Kayo; Hirabayashi, Daisuke; Enokida, Youichi [EcoTopia Science Institute, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, 464-8603 (Japan)

2007-07-01T23:59:59.000Z

265

Performance Demonstration Program Plan for Analysis of Simulated Headspace Gases  

SciTech Connect

The Performance Demonstration Program (PDP) for headspace gases distributes sample gases of volatile organic compounds (VOCs) for analysis. Participating measurement facilities (i.e., fixed laboratories, mobile analysis systems, and on-line analytical systems) are located across the United States. Each sample distribution is termed a PDP cycle. These evaluation cycles provide an objective measure of the reliability of measurements performed for transuranic (TRU) waste characterization. The primary documents governing the conduct of the PDP are the Quality Assurance Program Document (QAPD) (DOE/CBFO-94-1012) and the Waste Isolation Pilot Plant (WIPP) Waste Analysis Plan (WAP) contained in the Hazardous Waste Facility Permit (NM4890139088-TSDF) issued by the New Mexico Environment Department (NMED). The WAP requires participation in the PDP; the PDP must comply with the QAPD and the WAP. This plan implements the general requirements of the QAPD and the applicable requirements of the WAP for the Headspace Gas (HSG) PDP. Participating measurement facilities analyze blind audit samples of simulated TRU waste package headspace gases according to the criteria set by this PDP Plan. Blind audit samples (hereafter referred to as PDP samples) are used as an independent means to assess each measurement facilitys compliance with the WAP quality assurance objectives (QAOs). To the extent possible, the concentrations of VOC analytes in the PDP samples encompass the range of concentrations anticipated in actual TRU waste package headspace gas samples. Analyses of headspace gases are required by the WIPP to demonstrate compliance with regulatory requirements. These analyses must be performed by measurement facilities that have demonstrated acceptable performance in this PDP. These analyses are referred to as WIPP analyses and the TRU waste package headspace gas samples on which they are performed are referred to as WIPP samples in this document. Participating measurement facilities must analyze PDP samples using the same procedures used for routine waste characterization analyses of WIPP samples.

Carlsbad Field Office

2006-04-01T23:59:59.000Z

266

Analysis of greenhouse gases trading system using conversations among stakeholders  

Science Journals Connector (OSTI)

Greenhouse gas (GHG) reduction agreement makes up the targeted reduction of a legally binding GHG for each country or region. It enables us to buy and sell some GHG with other countries; it is the GHG trading system. But now, some free riders, ... Keywords: GHG emissions, GHG trading systems, MAS, agent-based modelling, agent-based systems, consumer behaviour, emissions reduction, free riders, genetic algorithms, global warming, greenhouse gases, multi-agent simulation, multi-agent systems

Setsuya Kurahashi; Masato Ohori

2010-08-01T23:59:59.000Z

267

Chemical production from industrial by-product gases: Final report  

SciTech Connect

The potential for conservation of natural gas is studied and the technical and economic feasibility and the implementation of ventures to produce such chemicals using carbon monoxide and hydrogen from byproduct gases are determined. A survey was performed of potential chemical products and byproduct gas sources. Byproduct gases from the elemental phosphorus and the iron and steel industries were selected for detailed study. Gas sampling, preliminary design, market surveys, and economic analyses were performed for specific sources in the selected industries. The study showed that production of methanol or ammonia from byproduct gas at the sites studied in the elemental phosphorus and the iron and steel industries is technically feasible but not economically viable under current conditions. Several other applications are identified as having the potential for better economics. The survey performed identified a need for an improved method of recovering carbon monoxide from dilute gases. A modest experimental program was directed toward the development of a permselective membrane to fulfill that need. A practical membrane was not developed but further investigation along the same lines is recommended. (MCW)

Lyke, S.E.; Moore, R.H.

1981-04-01T23:59:59.000Z

268

EIA-Voluntary Reporting of Greenhouse Gases Program - What's New  

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

Environment > Voluntary Reporting Program > What's New Environment > Voluntary Reporting Program > What's New Voluntary Reporting of Greenhouse Gases Program What's New Voluntary Reporting of Greenhouse Gases Program Suspended May 2011 The U.S. Energy Information Administration (EIA) Voluntary Reporting of Greenhouse Gases ("1605(b)") Program has been suspended. The suspension is due to recent reductions in budget appropriations and is effective immediately. Survey respondents may still submit data to the 1605(b) Program using the program's Workbook Form via EIA's Secure File Transfer mechanism. However, EIA will not be able to process and review submitted data or offer respondent support on the submitted data. Should a respondant submit data under the current collection cycle to EIA, the data will be retained in our electronic records. If the 1605(b) Program resumes normal operations, your submitted data will be reviewed and processed at that time. You will be notified in the future if the 1605(b) Program resumes normal operation. If you have any questions, please contact the survey manager, Paul McArdle, at paul.mcardle@eia.gov

269

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

270

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

271

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

272

A bridge-functional-based classical mapping method for predicting the correlation functions of uniform electron gases at finite temperature  

SciTech Connect

Efficient and accurate prediction of the correlation functions of uniform electron gases is of great importance for both practical and theoretical applications. This paper presents a bridge-functional-based classical mapping method for calculating the correlation functions of uniform spin-unpolarized electron gases at finite temperature. The bridge functional is formulated by following Rosenfeld's universality ansatz in combination with the modified fundamental measure theory. The theoretical predictions are in good agreement with recent quantum Monte Carlo results but with negligible computational cost, and the accuracy is better than a previous attempt based on the hypernetted-chain approximation. We find that the classical mapping method is most accurate if the effective mass of electrons increases as the density falls.

Liu, Yu; Wu, Jianzhong, E-mail: jwu@engr.ucr.edu [Department of Chemical and Environmental Engineering and Department of Mathematics, University of California, Riverside, California 92521 (United States)] [Department of Chemical and Environmental Engineering and Department of Mathematics, University of California, Riverside, California 92521 (United States)

2014-02-28T23:59:59.000Z

273

Removing Barriers to Interdisciplinary Research  

E-Print Network (OSTI)

A significant amount of high-impact contemporary scientific research occurs where biology, computer science, engineering and chemistry converge. Although programmes have been put in place to support such work, the complex dynamics of interdisciplinarity are still poorly understood. In this paper we interrogate the nature of interdisciplinary research and how we might measure its "success", identify potential barriers to its implementation, and suggest possible mechanisms for removing these impediments.

Naomi Jacobs; Martyn Amos

2010-12-19T23:59:59.000Z

274

Modeling Sustainable Agricultural Residue Removal at the Subfield Scale  

SciTech Connect

This study developed a computational strategy that utilizes data inputs from multiple spatial scales to investigate how variability within individual fields can impact sustainable residue removal for bioenergy production. Sustainable use of agricultural residues for bioenergy production requires consideration of the important role that residues play in limiting soil erosion and maintaining soil C, health, and productivity. Increased availability of subfield-scale data sets such as grain yield data, high-fidelity digital elevation models, and soil characteristic data provides an opportunity to investigate the impacts of subfield-scale variability on sustainable agricultural residue removal. Using three representative fields in Iowa, this study contrasted the results of current NRCS conservation management planning analysis with subfield-scale analysis for rake-and-bale removal of agricultural residue. The results of the comparison show that the field-average assumptions used in NRCS conservation management planning may lead to unsustainable residue removal decisions for significant portions of some fields. This highlights the need for additional research on subfield-scale sustainable agricultural residue removal including the development of real-time variable removal technologies for agricultural residue.

Muth, D.J.; McCorkle, D.S.; Koch, J.B.; Bryden, K.M.

2012-05-02T23:59:59.000Z

275

Air pollution policy in Europe: Quantifying the interaction with greenhouse gases and climate change policies  

Science Journals Connector (OSTI)

Abstract This paper uses the computable general equilibrium model WorldScan to analyse interactions between EU's air pollution and climate change policies. Covering the entire world and seven EU countries, WorldScan simulates economic growth in a neo-classical recursive dynamic framework, including emissions and abatement of greenhouse gases (CO2, N2O and CH4) and air pollutants (SO2, NOx, NH3 and PM2.5). Abatement includes the possibility of using end-of-pipe control options that remove pollutants without affecting the emission-producing activity itself. This paper analyses several variants of EU's air pollution policies for the year 2020. Air pollution policy will depend on end-of-pipe controls for not more than two thirds, thus also at least one third of the required emission reduction will come from changes in the use of energy through efficiency improvements, fuel switching and other structural changes in the economy. Greenhouse gas emissions thereby decrease, which renders climate change policies less costly. Our results show that carbon prices will fall, and may even drop to zero when the EU agrees on a more stringent air pollution policy.

Johannes Bollen; Corjan Brink

2014-01-01T23:59:59.000Z

276

Slang characterization and removal using pulse detonation technology during coal gasification  

SciTech Connect

Boiler slagging and fouling as a result of inorganic impurities in combustion gases being deposited on heat transfer tubes have caused severe problems in coal-fired power plant operation. These problems are fuel, system design, and operating condition dependent. Pulse detonation technology for the purpose of removing slag and fouling deposits in coal-fired utility power plant boilers offers great potential. The detonation wave technique based on high impact velocity with sufficient energy and thermal shock on the slag deposited on gas contact surfaces offers a convenient, inexpensive, yet efficient and effective way to supplement existing slag removal methods. These detonation waves have been demonstrated experimentally to have exceptionally high shearing capability important to the task of removing slag and fouling deposits. The experimental results show that the single shot detonation wave is capable of removing the entire slag (types of slag deposited on economizer) even at a distance of 8 in. from the exit of a detonation engine tube. Wave strength and slag orientation also have different effects on the chipping off of the slag. This paper discusses about the results obtained in effectively removing the economizer slag.

Huque, Z.; Mei, D.; Biney, P.O.; Zhou, J.

1997-03-25T23:59:59.000Z

277

Removal of Natural Steroid Hormones from Wastewater Using  

E-Print Network (OSTI)

Removal of Natural Steroid Hormones from Wastewater Using Membrane Contactor Processes J O S H U water resources and increased interest in wastewater reclamation for potable reuse. This interest has in the study of wastewater reuse in advanced life support systems (e.g., space missions) because

278

Libya HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Plan Libya HEU Removal Libya HEU Removal Location Libya United States 27 34' 9.5448" N, 17 24' 8.4384" E See map: Google Maps Javascript is required to view this map....

279

Canada HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Plan Canada HEU Removal Canada HEU Removal Location Canada United States 53 47' 24.972" N, 104 35' 23.4384" W See map: Google Maps Javascript is required to view this map....

280

Israel HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Plan Israel HEU Removal Israel HEU Removal Location Israel United States 30 53' 18.2328" N, 34 52' 14.178" E See map: Google Maps Javascript is required to view this map....

Note: This page contains sample records for the topic "gases removed increased" 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

Uzbekistan HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Uzbekistan HEU Removal Uzbekistan HEU Removal Location Uzbekistan United States 42 6' 56.196" N, 63 22' 8.9076" E See map: Google Maps Javascript is required to view this map...

282

France HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Four-Year Plan France HEU Removal France HEU Removal Location United States 45 44' 20.0544" N, 2 17' 6.5616" E See map: Google Maps Javascript is required to view this map...

283

Chile HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Four-Year Plan Chile HEU Removal Chile HEU Removal Location United States 25 28' 1.4916" S, 69 33' 55.548" W See map: Google Maps Javascript is required to view this map...

284

Taiwan HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Plan Taiwan HEU Removal Taiwan HEU Removal Location Taiwan United States 24 35' 37.4964" N, 120 53' 36.798" E See map: Google Maps Javascript is required to view this map....

285

Romania HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Plan Romania HEU Removal Romania HEU Removal Location Romania United States 45 47' 1.932" N, 24 41' 50.1576" E See map: Google Maps Javascript is required to view this map....

286

Serbia HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Plan Serbia HEU Removal Serbia HEU Removal Location Serbia United States 44 22' 45.7068" N, 20 26' 4.452" E See map: Google Maps Javascript is required to view this map....

287

Poland HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Plan Poland HEU Removal Poland HEU Removal Location Poland United States 53 23' 50.2872" N, 17 50' 30.4692" E See map: Google Maps Javascript is required to view this map....

288

Vietnam HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Plan Vietnam HEU Removal Vietnam HEU Removal Location Vietnam United States 13 12' 30.8628" N, 108 19' 30.702" E See map: Google Maps Javascript is required to view this map....

289

Ukraine HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Apply for Our Jobs Our Jobs Working at NNSA Blog Home content Four-Year Plan Ukraine HEU Removal Ukraine HEU Removal Location Ukraine United States 50 12' 24.8688" N,...

290

Japan HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Jobs Apply for Our Jobs Our Jobs Working at NNSA Blog Home content Four-Year Plan Japan HEU Removal Japan HEU Removal Location Japan United States 37 36' 59.5872" N, 140...

291

Performance Demonstration Program Plan for Analysis of Simulated Headspace Gases  

SciTech Connect

The Performance Demonstration Program (PDP) for headspace gases distributes blind audit samples in a gas matrix for analysis of volatile organic compounds (VOCs). Participating measurement facilities (i.e., fixed laboratories, mobile analysis systems, and on-line analytical systems) are located across the United States. Each sample distribution is termed a PDP cycle. These evaluation cycles provide an objective measure of the reliability of measurements performed for transuranic (TRU) waste characterization. The primary documents governing the conduct of the PDP are the Quality Assurance Program Document (QAPD) (DOE/CBFO-94-1012) and the Waste Isolation Pilot Plant (WIPP) Waste Analysis Plan (WAP) contained in the Hazardous Waste Facility Permit (NM4890139088-TSDF) issued by the New Mexico Environment Department (NMED). The WAP requires participation in the PDP; the PDP must comply with the QAPD and the WAP. This plan implements the general requirements of the QAPD and the applicable requirements of the WAP for the Headspace Gas (HSG) PDP. Participating measurement facilities analyze blind audit samples of simulated TRU waste package headspace gases according to the criteria set by this PDP Plan. Blind audit samples (hereafter referred to as PDP samples) are used as an independent means to assess each measurement facilitys compliance with the WAP quality assurance objectives (QAOs). To the extent possible, the concentrations of VOC analytes in the PDP samples encompass the range of concentrations anticipated in actual TRU waste package headspace gas samples. Analyses of headspace gases are required by the WIPP to demonstrate compliance with regulatory requirements. These analyses must be performed by measurement facilities that have demonstrated acceptable performance in this PDP. These analyses are referred to as WIPP analyses and the TRU waste package headspace gas samples on which they are performed are referred to as WIPP samples in this document. Participating measurement facilities must analyze PDP samples using the same procedures used for routine waste characterization analyses of WIPP samples.

Carlsbad Field Office

2007-11-19T23:59:59.000Z

292

Performance Demonstration Program Plan for Analysis of Simulated Headspace Gases  

SciTech Connect

The Performance Demonstration Program (PDP) for headspace gases distributes blind audit samples in a gas matrix for analysis of volatile organic compounds (VOCs). Participating measurement facilities (i.e., fixed laboratories, mobile analysis systems, and on-line analytical systems) are located across the United States. Each sample distribution is termed a PDP cycle. These evaluation cycles provide an objective measure of the reliability of measurements performed for transuranic (TRU) waste characterization. The primary documents governing the conduct of the PDP are the Quality Assurance Program Document (QAPD) (DOE/CBFO-94-1012) and the Waste Isolation Pilot Plant (WIPP) Waste Analysis Plan (WAP) contained in the Hazardous Waste Facility Permit (NM4890139088-TSDF) issued by the New Mexico Environment Department (NMED). The WAP requires participation in the PDP; the PDP must comply with the QAPD and the WAP. This plan implements the general requirements of the QAPD and the applicable requirements of the WAP for the Headspace Gas (HSG) PDP. Participating measurement facilities analyze blind audit samples of simulated TRU waste package headspace gases according to the criteria set by this PDP Plan. Blind audit samples (hereafter referred to as PDP samples) are used as an independent means to assess each measurement facilitys compliance with the WAP quality assurance objectives (QAOs). To the extent possible, the concentrations of VOC analytes in the PDP samples encompass the range of concentrations anticipated in actual TRU waste package headspace gas samples. Analyses of headspace gases are required by the WIPP to demonstrate compliance with regulatory requirements. These analyses must be performed by measurement facilities that have demonstrated acceptable performance in this PDP. These analyses are referred to as WIPP analyses and the TRU waste package headspace gas samples on which they are performed are referred to as WIPP samples in this document. Participating measurement facilities must analyze PDP samples using the same procedures used for routine waste characterization analyses of WIPP samples.

Carlsbad Field Office

2007-11-13T23:59:59.000Z

293

Remove Condensate with Minimal Air Loss  

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

This tip sheet outlines several condensate removal methods as part of maintaining compressed air system air quality.

294

Laser-based coatings removal  

SciTech Connect

Over the years as building and equipment surfaces became contaminated with low levels of uranium or plutonium dust, coats of paint were applied to stabilize the contaminants in place. Most of the earlier paint used was lead-based paint. More recently, various non-lead-based paints, such as two-part epoxy, are used. For D & D (decontamination and decommissioning), it is desirable to remove the paints or other coatings rather than having to tear down and dispose of the entire building.

Freiwald, J.G.; Freiwald, D.

1995-12-01T23:59:59.000Z

295

EIA-Voluntary Reporting of Greenhouse Gases Program - Reporting Guidelines  

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

Reporting Guidelines Reporting Guidelines Voluntary Reporting of Greenhouse Gases Program Reporting Guidelines The purpose of the guidelines is to establish the procedures and requirements for filing voluntary reports, and to ensure that the annual reports of greenhouse gas emissions, emission reductions, and sequestration activities submitted by corporations, government agencies, non-profit organizations, households, and other private and public entities to submit are complete, reliable, and consistent. Over time, it is anticipated that these reports will provide a reliable record of the contributions reporting entities have made toward reducing their greenhouse gas emissions. General Guidelines General Guidelines Technical Guidelines Technical Guidelines Appendices to the Technical Guidelines:

296

Prospecting by sampling and analysis of airborne particulates and gases  

DOE Patents (OSTI)

A method is claimed for prospecting by sampling airborne particulates or gases at a ground position and recording wind direction values at the time of sampling. The samples are subsequently analyzed to determine the concentrations of a desired material or the ratios of the desired material to other identifiable materials in the collected samples. By comparing the measured concentrations or ratios to expected background data in the vicinity sampled, one can select recorded wind directions indicative of the upwind position of the land-based source of the desired material.

Sehmel, G.A.

1984-05-01T23:59:59.000Z

297

Zero sound modes of dilute Fermi gases with arbitrary spin  

Science Journals Connector (OSTI)

Motivated by the recent success of optical trapping of alkali-metal bosons, we have studied the zero sound modes of dilute Fermi gases with arbitrary spin-f, which are spin-S excitations (0<~S<~2f). The dispersion of the mode (S) depends on a single Landau parameter F(S), which is related to the scattering lengths of the system through a simple formula. Measurement of (even a subset of) these modes in finite magnetic fields will enable one to determine all the interaction parameters of the system.

S.-K. Yip and Tin-Lun Ho

1999-06-01T23:59:59.000Z

298

Neutron removal cross section as a measure of neutron skin  

Science Journals Connector (OSTI)

We study the relation between neutron removal cross section (?-N) and neutron skin thickness for finite neutron-rich nuclei using the statistical abrasion ablation model. Different sizes of neutron skin are obtained by adjusting the diffuseness parameter of neutrons in the Fermi distribution. It is demonstrated that there is a good linear correlation between ?-N and the neutron skin thickness for neutron-rich nuclei. Further analysis suggests that the relative increase of neutron removal cross section could be used as a quantitative measure for neutron skin thickness in neutron-rich nuclei.

D. Q. Fang (???); Y. G. Ma (???); X. Z. Cai (???); W. D. Tian (???); H. W. Wang (???)

2010-04-07T23:59:59.000Z

299

Sorbents for the oxidation and removal of mercury  

DOE Patents (OSTI)

A promoted activated carbon sorbent is described that is highly effective for the removal of mercury from flue gas streams. The sorbent comprises a new modified carbon form containing reactive forms of halogen and halides. Optional components may be added to increase reactivity and mercury capacity. These may be added directly with the sorbent, or to the flue gas to enhance sorbent performance and/or mercury capture. Mercury removal efficiencies obtained exceed conventional methods. The sorbent can be regenerated and reused. Sorbent treatment and preparation methods are also described. New methods for in-flight preparation, introduction, and control of the active sorbent into the mercury contaminated gas stream are described.

Olson, Edwin S. (Grand Forks, ND); Holmes, Michael J. (Thompson, ND); Pavlish, John H. (East Grand Forks, MN)

2008-10-14T23:59:59.000Z

300

Sorbents for the oxidation and removal of mercury  

DOE Patents (OSTI)

A promoted activated carbon sorbent is described that is highly effective for the removal of mercury from flue gas streams. The sorbent comprises a new modified carbon form containing reactive forms of halogen and halides. Optional components may be added to increase reactivity and mercury capacity. These may be added directly with the sorbent, or to the flue gas to enhance sorbent performance and/or mercury capture. Mercury removal efficiencies obtained exceed conventional methods. The sorbent can be regenerated and reused. Sorbent treatment and preparation methods are also described. New methods for in-flight preparation, introduction, and control of the active sorbent into the mercury contaminated gas stream are described.

Olson, Edwin S.; Holmes, Michael J.; Pavlish, John Henry

2014-09-02T23:59:59.000Z

Note: This page contains sample records for the topic "gases removed increased" 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

SEPARATION OF CO2 FROM FLUE GASES BY CARBON-MULTIWALL CARBON NANOTUBE MEMBRANES  

SciTech Connect

Multiwalled carbon nanotubes (MWNT) were found to be an effective separation media for removing CO{sub 2} from N{sub 2}. The separation mechanism favors the selective condensation of CO{sub 2} from the flowing gas stream. Significant uptakes of CO{sub 2} were measured at 30 C and 150 C over the pressure range 0.5 to 5 bar. No measurable uptake of nitrogen was found for this range of conditions. The mass uptake of CO{sub 2} by MWNT was found to increase with increasing temperature. A packed bed of MWNT completely removed CO{sub 2} from a flowing stream of CO{sub 2}/N{sub 2}, and exhibited rapid uptake kinetics for CO{sub 2}.

Rodney Andrews

2001-03-01T23:59:59.000Z

302

Instantaneous and efficient surface wave excitation of a low pressure gas or gases  

DOE Patents (OSTI)

A system for instantaneously ionizing and continuously delivering energy in the form of surface waves to a low pressure gas or mixture of low pressure gases, comprising a source of rf energy, a discharge container, (such as a fluorescent lamp discharge tube), an rf shield, and a coupling device responsive to rf energy from the source to couple rf energy directly and efficiently to the gas or mixture of gases to ionize at least a portion of the gas or gases and to provide energy to the gas or gases in the form of surface waves. The majority of the rf power is transferred to the gas or gases near the inner surface of the discharge container to efficiently transfer rf energy as excitation energy for at least one of the gases. The most important use of the invention is to provide more efficient fluorescent and/or ultraviolet lamps.

Levy, Donald J. (Berkeley, CA); Berman, Samuel M. (San Francisco, CA)

1988-01-01T23:59:59.000Z

303

Method of making thermally removable epoxies  

DOE Patents (OSTI)

A method of making a thermally-removable epoxy by mixing a bis(maleimide) compound to a monomeric furan compound containing an oxirane group to form a di-epoxy mixture and then adding a curing agent at temperatures from approximately room temperature to less than approximately 90.degree. C. to form a thermally-removable epoxy. The thermally-removable epoxy can be easily removed within approximately an hour by heating to temperatures greater than approximately 90.degree. C. in a polar solvent. The epoxy material can be used in protecting electronic components that may require subsequent removal of the solid material for component repair, modification or quality control.

Loy, Douglas A. (Albuquerque, NM); Wheeler, David R. (Albuquerque, NM); Russick, Edward M. (Rio Rancho, NM); McElhanon, James R. (Albuquerque, NM); Saunders, Randall S. (late of Albuquerque, NM)

2002-01-01T23:59:59.000Z

304

Synthetic Lorentz force in classical atomic gases via Doppler effect and radiation pressure  

E-Print Network (OSTI)

We theoretically predict a novel type of synthetic Lorentz force for classical (cold) atomic gases, which is based on the Doppler effect and radiation pressure. A fairly uniform and strong force can be constructed for gases in macroscopic volumes of several cubic millimeters and more. This opens the possibility to mimic classical charged gases in magnetic fields, such as those in a tokamak, in cold atom experiments.

Dub?ek, T; Juki?, D; Aumiler, D; Ban, T; Buljan, H

2014-01-01T23:59:59.000Z

305

E-Print Network 3.0 - automobile exhaust gases Sample Search...  

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

exhaust gases Page: << < 1 2 3 4 5 > >> 1 Ability of Catalytic Converters to Reduce Air Pollution Summary: Air Pollution MEASUREMENT OF SELECTED AIR POLLUTANTS IN CAR EXHAUST...

306

E-Print Network 3.0 - aircraft exhaust gases Sample Search Results  

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

gases FAA, 2005. Water in the aircraft exhaust at altitude may have a greenhouse effect... . Aircraft ... Source: Ecole Polytechnique, Centre de mathmatiques...

307

Fact #825: June 16, 2014 Tier 3 Non-Methane Organic Gases Plus...  

Energy Savers (EERE)

organic gases (NMOG) and nitrogen oxides (NOx) that new light vehicles with gasoline engines are allowed to produce for model years 2017 to 2025. These standards apply to...

308

Nitrogen removal from natural gas  

SciTech Connect

According to a 1991 Energy Information Administration estimate, U.S. reserves of natural gas are about 165 trillion cubic feet (TCF). To meet the long-term demand for natural gas, new gas fields from these reserves will have to be developed. Gas Research Institute studies reveal that 14% (or about 19 TCF) of known reserves in the United States are subquality due to high nitrogen content. Nitrogen-contaminated natural gas has a low Btu value and must be upgraded by removing the nitrogen. In response to the problem, the Department of Energy is seeking innovative, efficient nitrogen-removal methods. Membrane processes have been considered for natural gas denitrogenation. The challenge, not yet overcome, is to develop membranes with the required nitrogen/methane separation characteristics. Our calculations show that a methane-permeable membrane with a methane/nitrogen selectivity of 4 to 6 would make denitrogenation by a membrane process viable. The objective of Phase I of this project was to show that membranes with this target selectivity can be developed, and that the economics of the process based on these membranes would be competitive. Gas permeation measurements with membranes prepared from two rubbery polymers and a superglassy polymer showed that two of these materials had the target selectivity of 4 to 6 when operated at temperatures below - 20{degrees}C. An economic analysis showed that a process based on these membranes is competitive with other technologies for small streams containing less than 10% nitrogen. Hybrid designs combining membranes with other technologies are suitable for high-flow, higher-nitrogen-content streams.

NONE

1997-04-01T23:59:59.000Z

309

Ceramic membrane reactor with two reactant gases at different pressures  

DOE Patents (OSTI)

The invention is a ceramic membrane reactor for syngas production having a reaction chamber, an inlet in the reactor for natural gas intake, a plurality of oxygen permeating ceramic slabs inside the reaction chamber with each slab having a plurality of passages paralleling the gas flow for transporting air through the reaction chamber, a manifold affixed to one end of the reaction chamber for intake of air connected to the slabs, a second manifold affixed to the reactor for removing the oxygen depleted air, and an outlet in the reaction chamber for removing syngas.

Balachandran, Uthamalingam (Hinsdale, IL); Mieville, Rodney L. (Glen Ellyn, IL)

2001-01-01T23:59:59.000Z

310

Carbon dioxide capture from power or process plant gases  

SciTech Connect

The present invention are methods for removing preselected substances from a mixed flue gas stream characterized by cooling said mixed flue gas by direct contact with a quench liquid to condense at least one preselected substance and form a cooled flue gas without substantial ice formation on a heat exchanger. After cooling additional process methods utilizing a cryogenic approach and physical concentration and separation or pressurization and sorbent capture may be utilized to selectively remove these materials from the mixed flue gas resulting in a clean flue gas.

Bearden, Mark D; Humble, Paul H

2014-06-10T23:59:59.000Z

311

GFDL One-Page Research Summary Mean climate controls on the simulated response of ENSO to increasing greenhouse gases  

E-Print Network (OSTI)

disasters, agriculture, fisheries, and natural ecosystems. Understanding and predicting the future behavior, this study presents the first comprehensive, pointwise, multi-model upper-ocean heat budget analysis of the pre-industrial control and doubled CO2 climate change experiments from the global coupled GCMs

312

Evaluation of an Unsuccessful Brook Trout Electrofishing Removal Project in a Small Rocky Mountain Stream.  

SciTech Connect

In the western United States, exotic brook trout Salvelinus fontinalis frequently have a deleterious effect on native salmonids, and biologists often attempt to remove brook trout from streams by means of electrofishing. Although the success of such projects typically is low, few studies have assessed the underlying mechanisms of failure, especially in terms of compensatory responses. A multiagency watershed advisory group (WAG) conducted a 3-year removal project to reduce brook trout and enhance native salmonids in 7.8 km of a southwestern Idaho stream. We evaluated the costs and success of their project in suppressing brook trout and looked for brook trout compensatory responses, such as decreased natural mortality, increased growth, increased fecundity at length, and earlier maturation. The total number of brook trout removed was 1,401 in 1998, 1,241 in 1999, and 890 in 2000; removal constituted an estimated 88% of the total number of brook trout in the stream in 1999 and 79% in 2000. Although abundance of age-1 and older brook trout declined slightly during and after the removals, abundance of age-0 brook trout increased 789% in the entire stream 2 years after the removals ceased. Total annual survival rate for age-2 and older brook trout did not decrease during the removals, and the removals failed to produce an increase in the abundance of native redband trout Oncorhynchus mykiss gairdneri. Lack of a meaningful decline and unchanged total mortality for older brook trout during the removals suggest that a compensatory response occurred in the brook trout population via reduced natural mortality, which offset the removal of large numbers of brook trout. Although we applaud WAG personnel for their goal of enhancing native salmonids by suppressing brook trout via electrofishing removal, we conclude that their efforts were unsuccessful and suggest that similar future projects elsewhere over such large stream lengths would be costly, quixotic enterprises.

Meyer, Kevin A.; Lamansky, Jr., James A.; Schill, Daniel J.

2006-01-26T23:59:59.000Z

313

NETL: News Release - DOE Seeks Cost-Shared Research Proposals to Remove  

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

March 20, 2000 March 20, 2000 DOE Seeks Cost-Shared Research Proposals to Remove Mercury From Coal-Fired Power Plants With the Environmental Protection Agency expected to decide in December whether to regulate mercury emissions from coal-burning boilers, the U.S. Department of Energy has kicked off a new effort to develop more affordable pollution control technologies that can remove mercury from power plant flue gases. The Energy Department, through its National Energy Technology Laboratory, has issued a solicitation offering up to $13 million over three years for industry proposals on cost-cutting mercury-control methods for coal-based power systems. Currently no technology exists that can uniformly control mercury from power plant flue gas emissions. The effectiveness of existing flue gas emission controls in removing mercury can vary considerably from plant to plant, or even from boiler to boiler. With today's technologies, mercury removal can range from essentially no control to as high as 90 percent.

314

Method of removing nitrogen monoxide from a nitrogen monoxide-containing gas using a water-soluble iron ion-dithiocarbamate, xanthate or thioxanthate  

DOE Patents (OSTI)

A method of removing nitrogen monoxide from a nitrogen monoxide-containing gas, which method comprises: (a) contacting a nitrogen oxide-containing gas with an aqueous solution of water soluble organic compound-iron ion chelate of the formula: ##STR1## wherein the water-soluble organic compound is selected from compounds of the formula: ##STR2## wherein: R is selected from hydrogen or an organic moiety having at least one polar functional group; Z is selected from oxygen, sulfur, or --N--A wherein N is nitrogen and A is hydrogen or lower alkyl having from one to four carbon atoms; and M is selected from hydrogen, sodium or potassium; and n is 1 or 2, in a contacting zone for a time and at a temperature effective to reduce the nitrogen monoxide. These mixtures are useful to provide an unexpensive method of removing NO from gases, thus reducing atmospheric pollution from flue gases.

Liu, David K. (San Pablo, CA); Chang, Shih-Ger (El Cerrito, CA)

1989-01-01T23:59:59.000Z

315

Mercury removal in utility wet scrubber using a chelating agent  

DOE Patents (OSTI)

A method for capturing and reducing the mercury content of an industrial flue gas such as that produced in the combustion of a fossil fuel or solid waste adds a chelating agent, such as ethylenediaminetetraacetic acid (EDTA) or other similar compounds like HEDTA, DTPA and/or NTA, to the flue gas being scrubbed in a wet scrubber used in the industrial process. The chelating agent prevents the reduction of oxidized mercury to elemental mercury, thereby increasing the mercury removal efficiency of the wet scrubber. Exemplary tests on inlet and outlet mercury concentration in an industrial flue gas were performed without and with EDTA addition. Without EDTA, mercury removal totaled 42%. With EDTA, mercury removal increased to 71%. The invention may be readily adapted to known wet scrubber systems and it specifically provides for the removal of unwanted mercury both by supplying S.sup.2- ions to convert Hg.sup.2+ ions into mercuric sulfide (HgS) and by supplying a chelating agent to sequester other ions, including but not limited to Fe.sup.2+ ions, which could otherwise induce the unwanted reduction of Hg.sup.2+ to the form, Hg.sup.0.

Amrhein, Gerald T. (Louisville, OH)

2001-01-01T23:59:59.000Z

316

A method for removing arm backscatter from EPID images  

SciTech Connect

Purpose: To develop a method for removing the support arm backscatter from images acquired using current Varian electronic portal imaging devices (EPIDs).Methods: The effect of arm backscatter on EPID images was modeled using a kernel convolution method. The parameters of the model were optimized by comparing on-arm images to off-arm images. The model was used to develop a method to remove the effect of backscatter from measured EPID images. The performance of the backscatter removal method was tested by comparing backscatter corrected on-arm images to measured off-arm images for 17 rectangular fields of different sizes and locations on the imager. The method was also tested using on- and off-arm images from 42 intensity modulated radiotherapy (IMRT) fields.Results: Images generated by the backscatter removal method gave consistently better agreement with off-arm images than images without backscatter correction. For the 17 rectangular fields studied, the root mean square difference of in-plane profiles compared to off-arm profiles was reduced from 1.19% (standard deviation 0.59%) on average without backscatter removal to 0.38% (standard deviation 0.18%) when using the backscatter removal method. When comparing to the off-arm images from the 42 IMRT fields, the mean {gamma} and percentage of pixels with {gamma} < 1 were improved by the backscatter removal method in all but one of the images studied. The mean {gamma} value (1%, 1 mm) for the IMRT fields studied was reduced from 0.80 to 0.57 by using the backscatter removal method, while the mean {gamma} pass rate was increased from 72.2% to 84.6%.Conclusions: A backscatter removal method has been developed to estimate the image acquired by the EPID without any arm backscatter from an image acquired in the presence of arm backscatter. The method has been shown to produce consistently reliable results for a wide range of field sizes and jaw configurations.

King, Brian W. [School of Mathematical and Physics Sciences, University of Newcastle, Newcastle, New South Wales 2308 (Australia); Greer, Peter B. [Department of Radiation Oncology, Calvary Mater Newcastle Hospital, Newcastle, New South Wales 2310 (Australia); School of Mathematical and Physical Sciences, University of Newcastle, Newcastle, New South Wales 2308 (Australia)

2013-07-15T23:59:59.000Z

317

EIA-Voluntary Reporting of Greenhouse Gases Program - Why Report  

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

Why Report Why Report Voluntary Reporting of Greenhouse Gases Program Why Report What Is the Purpose of Form EIA-1605? Form EIA-1605 provides the means for the voluntary reporting of greenhouse gas emissions, reductions, and sequestration under Section 1605(b) of the Energy Policy Act of 1992. The purpose of the Voluntary Reporting Program is to encourage corporations, government agencies, non-profit organizations, households, and other private and public entities to submit annual reports of their greenhouse gas emissions, emission reductions, and sequestration activities. Form EIA-1605 provides a means for voluntary reporting that is complete, reliable, and consistent. How Will My Entity Benefit From Reporting? There are a number of ways for your entity to benefit from reporting, including:

318

Simulations of Deflagration-to-Detonation Transition in Reactive Gases |  

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

numerically generated pseudo-schlieren image numerically generated pseudo-schlieren image Weak ignition behind a reflected Mach=1.5 shock in a stoichiometric hydrogen-oxygen mixture at 0.1 atm initial pressure. Picture shows a numerically generated pseudo-schlieren image of the onset of a detonation in a turbulent boundary layer. Alexei Khokhlov, University of Chicago; Charles Bacon, Argonne National Laboratory, Joanna Austin, Andrew Knisely, University of Illinois at Urbanna-Champaign Simulations of Deflagration-to-Detonation Transition in Reactive Gases PI Name: Alexei Khokhlov PI Email: ajk@oddjob.uchicago.edu Institution: The University of Chicago Allocation Program: INCITE Allocation Hours at ALCF: 130 Million Year: 2013 Research Domain: Chemistry Hydrogen is an abundant, environmentally friendly fuel with the potential

319

Assess Potential Agency Size Changes that Impact Greenhouse Gases from  

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

Employee Commuting Employee Commuting Assess Potential Agency Size Changes that Impact Greenhouse Gases from Employee Commuting October 7, 2013 - 1:42pm Addthis YOU ARE HERE Step 1 For employee commuting, it is important to account for any planned or expected changes in a Federal agency's size when estimating the greenhouse gas (GHG) reduction potential for different operating units or worksites. Considerations include: Are employment levels expected to change in the next decade at specific facilities or agency-wide? Are there any planned facility moves at major worksites? Employee commute coordinators may want to engage human resources and strategic planners in this effort to establish likely changes in employment numbers. Facility planners may be engaged to understand changes in commutes

320

The Breakdown of Gases in High Frequency Electrical Fields  

Science Journals Connector (OSTI)

A theory is proposed to explain the mechanism of breakdown of gases in high frequency electrical fields. It is assumed that breakdown occurs when the electrical field and the frequency are such that an electron acquires the ionizing energy at the end of one mean free path. The field for breakdown is thus a function of the frequency of the applied potential and the ionization potential and pressure of the gas. The fields for breakdown of argon and xenon are calculated and expressed as functions of the frequency and the gas pressure. The calculated potentials are compared with experimental data, and good agreement is found for frequencies greater than 10106 c.p.s.

Donald H. Hale

1948-05-01T23:59:59.000Z

Note: This page contains sample records for the topic "gases removed increased" 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

WIMP Dark Matter Direct-Detection Searches in Noble Gases  

E-Print Network (OSTI)

Cosmological observations and the dynamics of the Milky Way provide ample evidence for an invisible and dominant mass component. This so-called dark matter could be made of new, colour and charge neutral particles, which were non-relativistic when they decoupled from ordinary matter in the early universe. Such weakly interacting massive particles (WIMPs) are predicted to have a non-zero coupling to baryons and could be detected via their collisions with atomic nuclei in ultra-low background, deep underground detectors. Among these, detectors based on liquefied noble gases have demonstrated tremendous discovery potential over the last decade. After briefly introducing the phenomenology of direct dark matter detection, I will review the main properties of liquefied argon and xenon as WIMP targets and discuss sources of background. I will then describe existing and planned argon and xenon detectors that employ the so-called single- and dual-phase detection techniques, addressing their complementarity and science...

Baudis, Laura

2014-01-01T23:59:59.000Z

322

WIMP Dark Matter Direct-Detection Searches in Noble Gases  

E-Print Network (OSTI)

Cosmological observations and the dynamics of the Milky Way provide ample evidence for an invisible and dominant mass component. This so-called dark matter could be made of new, colour and charge neutral particles, which were non-relativistic when they decoupled from ordinary matter in the early universe. Such weakly interacting massive particles (WIMPs) are predicted to have a non-zero coupling to baryons and could be detected via their collisions with atomic nuclei in ultra-low background, deep underground detectors. Among these, detectors based on liquefied noble gases have demonstrated tremendous discovery potential over the last decade. After briefly introducing the phenomenology of direct dark matter detection, I will review the main properties of liquefied argon and xenon as WIMP targets and discuss sources of background. I will then describe existing and planned argon and xenon detectors that employ the so-called single- and dual-phase detection techniques, addressing their complementarity and science reach.

Laura Baudis

2014-08-19T23:59:59.000Z

323

Highly polarized Fermi gases across a narrow Feshbach resonance  

Science Journals Connector (OSTI)

We address the phase of a highly polarized Fermi gases across a narrow Feshbach resonance starting from the problem of a single down-spin fermion immersed in a Fermi sea of up spins. Both polaron and pairing states are considered using the variational wave function approach, and we find that the polaron-to-pairing transition will take place on the BCS side of the resonance, strongly in contrast to a wide resonance where the transition is located at the BEC side. For the pairing phase, we find the critical strength of the repulsive interaction between pairs above which the mixture of pairs and fermions will not phase separate. Therefore, nearby a narrow resonance, it is quite likely that magnetism can coexist with s-wave BCS superfluidity at large Zeeman fields, which is a remarkable property absent in conventional BCS superconductors (or fermion-pair superfluids).

Ran Qi and Hui Zhai

2012-04-13T23:59:59.000Z

324

Finite-size energy of non-interacting Fermi gases  

E-Print Network (OSTI)

We prove the asymptotics of the difference of the ground-state energies of two non-interacting $N$-particle Fermi gases on the half line of length $L$ in the thermodynamic limit up to order $1/L$. We are particularly interested in subdominant terms proportional to $1/L$, called finite-size energy. In the nineties Affleck and co-authors [Aff97, ZA97, AL94] claimed that the finite-size energy equals the decay exponent occuring in Anderson's orthogonality catastrophe. It turns out that the finite-size energy depends on the details of the thermodynamic limit and typically also includes a linear term in the scattering phase shift.

Martin Gebert

2014-06-14T23:59:59.000Z

325

Granular Gases of Rod-Shaped Grains in Microgravity  

Science Journals Connector (OSTI)

Granular gases are convenient model systems to investigate the statistical physics of nonequilibrium systems. In the literature, one finds numerous theoretical predictions, but only few experiments. We study a weakly excited dilute gas of rods, confined in a cuboid container in microgravity during a suborbital rocket flight. With respect to a gas of spherical grains at comparable filling fraction, the mean free path is considerably reduced. This guarantees a dominance of grain-grain collisions over grain-wall collisions. No clustering was observed, unlike in similar experiments with spherical grains. Rod positions and orientations were determined and tracked. Translational and rotational velocity distributions are non-Gaussian. Equipartition of kinetic energy between translations and rotations is violated.

K. Harth; U. Kornek; T. Trittel; U. Strachauer; S. Hme; K. Will; R. Stannarius

2013-04-02T23:59:59.000Z

326

Carrier cooling and exciton formation in GaSe  

Science Journals Connector (OSTI)

The initial cooling of hot carriers and the subsequent exciton formation in GaSe are studied by time-resolved photoluminescence (PL) using femtosecond up-conversion techniques. From the time-resolved PL spectra of this layered III-VI semiconductor two different energy relaxation channels are derived. After an initial subpicosecond cooling due to Frhlich-type interaction of carriers with longitudinal optical E?(22) phonons a slower regime follows, which is dominated by deformation potential interaction with the nonpolar optical A1?(12) phonons. The coupling constant for nonpolar optical phonon scattering is derived. The subsequent formation of excitons is studied at different carrier densities and detection energies. A cross section for the free-exciton formation is determined based on a rate equation model.

S. Nsse; P. Haring Bolivar; H. Kurz; V. Klimov; F. Levy

1997-08-15T23:59:59.000Z

327

Kovacs-like memory effect in driven granular gases  

E-Print Network (OSTI)

While memory effects have been reported for dense enough disordered systems such as glasses, we show here by a combination of analytical and simulation techniques that they are also intrinsic to the dynamics of dilute granular gases. By means of a certain driving protocol, we prepare the gas in a state where the granular temperature $T$ coincides with its long time limit. However, $T$ does not subsequently remain constant, but exhibits a non-monotonic evolution before reaching its non-equilibrium steady value. The corresponding so-called Kovacs hump displays a normal behavior for weak dissipation (as observed in molecular systems), but is reversed under strong dissipation, where it thus becomes anomalous.

A. Prados; E. Trizac

2014-04-24T23:59:59.000Z

328

Sorption of organic gases in a furnished room  

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

a furnished room a furnished room Title Sorption of organic gases in a furnished room Publication Type Journal Article LBNL Report Number LBNL-53943 Year of Publication 2004 Authors Singer, Brett C., Kenneth L. Revzan, Toshifumi Hotchi, Alfred T. Hodgson, and Nancy J. Brown Journal Atmospheric Environment Volume 38 Start Page Chapter Issue 16 Pagination 2483-2494 Abstract We present experimental data and semi-empirical models describing the sorption of organic gases in a simulated indoor residential environment. Two replicate experiments were conducted with 20 volatile organic compounds (VOCs) in a 50-m3 room finished with painted wallboard, carpet and cushion, draperies and furnishings. The VOCs span a wide volatility range and include ten Hazardous Air Pollutants. VOCs were introduced to the static chamber as a pulse and their gas-phase concentrations were measured during a net adsorption period and a subsequent net desorption period. Three sorption models were fit to the measured concentrations for each compound to determine the simplest formulation needed to adequately describe the observed behavior. Sorption parameter values were determined by fitting the models to adsorption period data then checked by comparing measured and predicted behavior during desorption. The adequacy of each model was evaluated using a goodness of fit parameter calculated for each period. Results indicate that sorption usually does not greatly affect indoor concentrations of methyl-tert-butyl ether, 2-butanone, isoprene and benzene. In contrast, sorption appears to be a relevant indoor process for many of the VOCs studied, including C8-C10 aromatic hydrocarbons (HC), terpenes, and pyridine. These compounds sorbed at rates close to typical residential air change rates and exhibited substantial sorptive partitioning at equilibrium. Polycyclic aromatic HCs, aromatic alcohols, ethenylpyridine and nicotine initially adsorbed to surfaces at rates of 1.5 to >6 h-1 and partitioned 95 to >99% in the sorbed phase at equilibrium

329

Part 3: Removal Action | Department of Energy  

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

3: Removal Action 3: Removal Action Part 3: Removal Action Question: When may removal actions be initiated? Answer: Removal actions may be initiated when DOE determines that the action will prevent, minimize, stabilize, or eliminate a risk to health or the environment. The NCP specifies that the determination that a risk to health or the environment is appropriate for removal action should be based on: actual or potential exposure of humans, animals, or the food chain the presence of contained hazardous substances that pose a threat of release the threat of migration of the hazardous substances the threat of fire or explosion the availability of an appropriate Federal or State response capability [section 300.415(b)(2)]. In essence, where DOE identifies a threat of exposure to or migration of

330

TMI-2 reactor vessel head removal  

SciTech Connect

This report describes the safe removal and storage of the Three Mile Island Unit 2 reactor vessel head. The head was removed in July 1984 to permit the removal of the plenum and the reactor core, which were damaged during the 1979 accident. From July 1982, plans and preparations were made using a standard head removal procedure modified by the necessary precautions and changes to account for conditions caused by the accident. After data acquisition, equipment and structure modifications, and training the head was safely removed and stored and the internals indexing fixture and a work platform were installed on top of the vessel. Dose rates during and after the operation were lower than expected; lessons were learned from the operation which will be applied to the continuing fuel removal operations activities.

Bengel, P.R.; Smith, M.D.; Estabrook, G.A.

1984-12-01T23:59:59.000Z

331

TMI-2 reactor vessel head removal  

SciTech Connect

This report describes the safe removal and storage of the Three Mile Island Unit 2 (TMI-2) reactor vessel head. The head was removed in July 1984 to permit the removal of the plenum and the reactor core, which were damaged during the 1979 accident. From July 1982, plans and preparations were made using a standard head removal procedure modified by the necessary precautions and changes to account for conditions caused by the accident. After data acquisition, equipment and structure modifications, and training, the head was safely removed and stored; and the internals indexing fixture and a work platform were installed on top of the vessel. Dose rates during and after the operation were lower than expected; lessons were learned from the operation which will be applied to the continuing fuel removal operations activities.

Bengel, P.R.; Smith, M.D.; Estabrook, G.A.

1985-09-01T23:59:59.000Z

332

Are Greenhouse Gases Changing ENSO Precursors in the Western North Pacific?  

SciTech Connect

Using multiple observational and modeling datasets, we document a strengthening relationship between boreal winter sea surface temperature anomalies (SSTA) in the western North Pacific (WNP) and the development of the El Nino-Southern Oscillation (ENSO) one year later. The increased WNP-ENSO association emerged in the mid 20th century and has grown through the present, reaching correlation coefficients as high as ~0.70 in recent decades. Fully coupled climate experiments with the Community Earth System Model (CESM) replicate the WNP-ENSO association and indicate that greenhouse gases (GHG) are largely responsible for the observed increase. We speculate that shifts in the location and amplitudes of positive SST trends in the subtropical-tropical western Pacific impacts the low-level circulation so that WNP variability is increasingly influencing the development of ENSO one year later. A strengthened GHG-driven relationship between the WNP and ENSO provides an example of how anthropogenic climate change can potentially improve the skill of intraseasonal-to-interannual climate prediction.

Wang, S-Y (Simon); Heureux, Michelle L.; Yoon, Jin-Ho

2013-09-01T23:59:59.000Z

333

Process for particulate removal from coal liquids  

DOE Patents (OSTI)

Suspended solid particulates are removed from liquefied coal products by first subjecting such products to hydroclone action for removal in the underflow of the larger size particulates, and then subjecting the overflow from said hydroclone action, comprising the residual finer particulates, to an electrostatic field in an electrofilter wherein such finer particulates are deposited in the bed of beads of dielectric material on said filter. The beads are periodically cleaned by backwashing to remove the accumulated solids.

Rappe, Gerald C. (Macungie, PA)

1983-01-01T23:59:59.000Z

334

Install Removable Insulation on Valves and Fittings  

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

This tip sheet on installing removable insulation on valves and fittings provides how-to advice for improving steam systems using low-cost, proven practices and technologies.

335

Method of making thermally removable polymeric encapsulants  

DOE Patents (OSTI)

A method of making a thermally-removable encapsulant by heating a mixture of at least one bis(maleimide) compound and at least one monomeric tris(furan) or tetrakis(furan) compound at temperatures from above room temperature to less than approximately 90.degree. C. to form a gel and cooling the gel to form the thermally-removable encapsulant. The encapsulant can be easily removed within approximately an hour by heating to temperatures greater than approximately 90.degree. C., preferably in a polar solvent. The encapsulant can be used in protecting electronic components that may require subsequent removal of the encapsulant for component repair, modification or quality control.

Small, James H. (Santa Fe, NM); Loy, Douglas A. (Albuquerque, NM); Wheeler, David R. (Albuquerque, NM); McElhanon, James R. (Albuquerque, NM); Saunders, Randall S. (late of Albuquerque, NM)

2001-01-01T23:59:59.000Z

336

Australia HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Australia HEU Removal | National Nuclear Security Administration Facebook Twitter Youtube Flickr RSS People Mission Managing the Stockpile Preventing Proliferation Powering the...

337

Argentina HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Argentina HEU Removal | National Nuclear Security Administration Facebook Twitter Youtube Flickr RSS People Mission Managing the Stockpile Preventing Proliferation Powering the...

338

Keeler-Pennwalt Wood Pole Removal  

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

natural environment. The entire remaining length of the Keeler-Pennwalt transmission line, from Keeler Substation to Structure 96, will be removed (approximately 9 miles)....

339

Efficiency of partial water removal during transmission of steam-water mixture on geothermal fields  

Science Journals Connector (OSTI)

The partial water removal from a steam-water mixture before transmission to prevent a pipeline from entering pulsation mode and to increase the flow of the heat carrier coming to the geothermal power plant is ...

A. N. Shulyupin

2007-10-01T23:59:59.000Z

340

Theory of the lattice Boltzmann method: Lattice Boltzmann models for nonideal gases Li-Shi Luo*  

E-Print Network (OSTI)

Theory of the lattice Boltzmann method: Lattice Boltzmann models for nonideal gases Li-Shi Luo is presented. This treat- ment provides a unified theory of lattice Boltzmann models for nonideal gases. The lattice Boltzmann equation is systematically obtained by discretizing the Enskog equation in phase space

Luo, Li-Shi

Note: This page contains sample records for the topic "gases removed increased" 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

Preserving noble gases in a convecting mantle Helge M. Gonnermann1  

E-Print Network (OSTI)

of a processed and out- gassed lower-mantle source, residues of mantle melting10,11 , depleted in uranium and mixing of noble-gas-depleted slabs dilutes the concentrations of noble gases in the mantle, thereby melt, which forms the ocean crust and leaves the residual mantle severely depleted of noble gases

Mukhopadhyay, Sujoy

342

Helium Isotopes In Geothermal And Volcanic Gases Of The Western United  

Open Energy Info (EERE)

Helium Isotopes In Geothermal And Volcanic Gases Of The Western United Helium Isotopes In Geothermal And Volcanic Gases Of The Western United States, I, Regional Variability And Magmatic Origin Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Journal Article: Helium Isotopes In Geothermal And Volcanic Gases Of The Western United States, I, Regional Variability And Magmatic Origin Details Activities (1) Areas (1) Regions (0) Abstract: Helium isotope ratios in gases of thirty hot springs and geothermal wells and of five natural gas wells in the western United States show no relationship to regional conductive heat flow, but do show a correlation with magma-based thermal activity and reservoir fluid temperature (or total convective heat discharge). Gases from high-T (> 200°C) reservoirs have 3He/4He > 2 _ the atmospheric value, with high He

343

Acid dyes removal using low cost adsorbents  

Science Journals Connector (OSTI)

Dyestuff production units and dyeing units have always had pressing need techniques that allow economical pre-treatment for colour in the effluent. The effectiveness of adsorption for dye removal from wastewaters has made it an ideal alternative to other expensive treatment options. Removal of acid green

A.H. Aydin; Y. Bulut; O. Yavuz

2004-01-01T23:59:59.000Z

344

COST OF MERCURY REMOVAL IN IGCC PLANTS  

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

Cost of Mercury Removal Cost of Mercury Removal in an IGCC Plant Final Report September 2002 Prepared for: The United States Department of Energy National Energy Technology Laboratory By: Parsons Infrastructure and Technology Group Inc. Reading, Pennsylvania Pittsburgh, Pennsylvania DOE Product Manager: Gary J. Stiegel DOE Task Manager: James R. Longanbach Principal Investigators: Michael G. Klett Russell C. Maxwell Michael D. Rutkowski PARSONS The Cost of Mercury Removal in an IGCC Plant Final Report i September 2002 TABLE OF CONTENTS Section Title Page 1 Summary 1 2 Introduction 3 3 Background 4 3.1 Regulatory Initiatives 4 3.2 Mercury Removal for Conventional Coal-Fired Plants 4 3.3 Mercury Removal Experience in Gasification 5 3.4 Variability of Mercury Content in Coal 6 4 Design Considerations 7 4.1 Carbon Bed Location

345

Residential propane prices increase  

Annual Energy Outlook 2012 (EIA)

propane prices increase The average retail price for propane rose 3.2 cents from a week ago to 2.86 per gallon. That's up 59.3 cents from a year ago, based on the residential...

346

Residential propane prices increase  

Gasoline and Diesel Fuel Update (EIA)

propane prices increase The average retail price for propane rose 10.3 cents from a week ago to 2.96 per gallon. That's up 68.1 cents from a year ago, based on the residential...

347

Residential propane prices increase  

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

propane prices increase The average retail price for propane rose 3.9 cents from a week ago to 2.80 per gallon. That's up 53.7 cents from a year ago, based on the residential...

348

Residential propane prices increase  

Annual Energy Outlook 2012 (EIA)

propane prices increase The average retail price for propane rose 5.5 cents per gallon from last week to 2.62 per gallon; up 37.4 cents from a year ago, based on the residential...

349

Residential propane price increases  

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

propane price increases The average retail price for propane is 2.41 per gallon, up 6-tenths of a cent from last week, based on the residential heating fuel survey by the U.S....

350

Residential propane prices increase  

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

propane prices increase The average retail price for propane rose 4.8 cents from a week ago to 2.76 per gallon. That's up 51.2 cents from a year ago, based on the residential...

351

Residential propane prices increase  

Gasoline and Diesel Fuel Update (EIA)

propane prices increase The average retail price for propane rose 2.5 cents from a week ago to 2.83 per gallon. That's up 56 cents from a year ago, based on the residential...

352

Residential propane prices increase  

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

propane prices increase The average retail price for propane rose to 2.40 per gallon, up 1.1 cents from a week ago, based on the residential heating fuel survey by the U.S. Energy...

353

Residential propane prices increase  

Annual Energy Outlook 2012 (EIA)

propane prices increase The average retail price for propane rose 2.3 cents per gallon from last week to 2.57 per gallon; up 32.2 cents from a year ago, based on the residential...

354

Residential propane prices increase  

Gasoline and Diesel Fuel Update (EIA)

propane prices increase The average retail price for propane rose 9.1 cents from a week ago to 2.71 per gallon. That's up 46.9 cents from a year ago, based on the residential...

355

Leptin increases maternal investment  

Science Journals Connector (OSTI)

...articles 1001 14 Leptin increases maternal investment Susannah S. French 1 * Timothy J...between self-maintenance and offspring investment when resources are limited. In the...effects of elevated maternal leptin on investment into offspring production versus self...

2009-01-01T23:59:59.000Z

356

Diesel prices increase  

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

Diesel prices increase The U.S. average retail price for on-highway diesel fuel rose to 3.90 a gallon on Monday. That's up 3 cents from a week ago, based on the weekly price...

357

Use of hollow core fibers, fiber lasers, and photonic crystal fibers for spark delivery and laser ignition in gases  

Science Journals Connector (OSTI)

The fiber-optic delivery of sparks in gases is challenging as the output beam must be refocused to high

Joshi, Sachin; Yalin, Azer P; Galvanauskas, Almantas

2007-01-01T23:59:59.000Z

358

ADVANCES IN HEXAVALENT CHROMIUM REMOVAL AT HANFORD  

SciTech Connect

At the Hanford Site, chromium was used as a corrosion inhibitor in the reactor cooling water and was introduced into the groundwater as a result of planned and unplanned discharges from reactors during plutonium production since 1944. Beginning in 1995, groundwater treatment methods were evaluated leading to the use of pump and treat facilities with ion exchange using Dowex 21 K, a regenerable strong base anion exchange resin. This required regeneration of the resin, which is currently performed offsite. Resin was installed in a 4 vessel train, with resin removal required from the lead vessel approximately once a month. In 2007, there were 8 trains (32 vessels) in operation. In 2008, DOE recognized that regulatory agreements would require significant expansion in the groundwater chromium treatment capacity. Previous experience from one of the DOE project managers led to identification of a possible alternative resin, and the contractor was requested to evaluate alternative resins for both cost and programmatic risk reductions. Testing was performed onsite in 2009 and 2010, using a variety of potential resins in two separate facilities with groundwater from specific remediation sites to demonstrate resin performance in the specific groundwater chemistry at each site. The testing demonstrated that a weak base anion single-use resin, ResinTech SIR-700, was effective at removing chromium, had a significantly higher capacity, could be disposed of efficiently on site, and would eliminate the complexities and programmatic risks from sampling, packaging, transportation and return of resin for regeneration. This resin was installed in Hanford's newest groundwater treatment facility, called 100-DX, which began operations in November, 2010, and used in a sister facility, 100-HX, which started up in September of 2011. This increased chromium treatment capacity to 25 trains (100 vessels). The resin is also being tested in existing facilities that utilize Dowex 21 K for conversion to the new resin. This paper will describe the results of the testing, performance in the facilities, continued optimization in the pump and treat facilities, and the estimated savings and non-tangible benefits of the conversion.

NESHEM DO; RIDDELLE J

2012-01-30T23:59:59.000Z

359

Carbon dioxide removal and capture for landfill gas up-grading  

Science Journals Connector (OSTI)

Within the frame of an EC financially supported project - LIFE05 ENV/IT/000874 GHERL (Greenhouse Effect Reduction from Landfill)a pilot plant was set up in order to demonstrate the feasibility of applying chemical absorption to remove carbon dioxide from landfill gas. After proper upgrading - basically removal of carbon dioxide, hydrogen sulphide, ammonia and other trace gas compoundthe gas might be fed into the distribution grid for natural gas or used as vehicle fuel, replacing a fossil fuel thus saving natural resources and carbon dioxide emissions. Several experiences in Europe have been carried out concerning the landfill gas - and biogas from anaerobic digestion - quality up-grading through CO2 removal, but in all of them carbon dioxide was vented to the atmosphere after separation, without any direct benefit in terms of greenhouse gases reduction. With respect to those previous experiences, in this work the attention was focused on CO2 removal from landfill gas with an effective capture process, capable of removing carbon dioxide from atmosphere, through a globally carbon negative process. In particular, processes capable of producing final solid products were investigated, with the aim of obtaining as output solid compounds which can be either used in the chemical industry or disposed off. The adopted absorption process is based on using aqueous solutions of potassium hydroxide, with the final aim of producing potassium carbonate. Potassium carbonate is a product which has several applications in the chemical industry if obtained with adequate quality. It can be sold as a pulverised solid, or in aqueous solution. Several tests were carried out at the pilot plant, which was located at a landfill site, in order to feed it with a fraction of the on-site collected landfill gas. The results of the experimental campaign are reported, explained and commented in the paper. Also a discussion on economic issues is presented.

Lidia Lombardia; Andrea Corti; Ennio Carnevale; Renato Baciocchi; Daniela Zingaretti

2011-01-01T23:59:59.000Z

360

Rapid?sampling system for dusts and gases  

Science Journals Connector (OSTI)

The Bureau of Mines has developed a system for the rapid grab sampling of heterogeneous mixtures of gases and dusts during the preignition and postignition stages of dust explosions. The combustion chamber in which the explosion occurs is first fitted with a hypodermic sampling needle with its inlet end at the desired sampling point within the chamber and its sharp injecting end protruding outside of the chamber. Rapid sampling (approximately 25 to 50 ms) is achieved with a double?acting air?pressure?actuated cylinder. The forward stroke of the cylinder thrusts the rubber septum seal of an evacuated glass sampling tube onto the protruding needle which punctures the septum filling the tube with gas and dust from the combustion chamber. The return stroke of the cylinder reseals the sampling tube by returning the mechanism to its original position. The initial time of sampling and the duration of sampling are independently variable and controlled by a microprocessor. Results obtained with a trimodal distribution of coal dust show no significant size discrimination at least up to 70 ?m. Data obtained from laboratory?scale coal dust explosion tests are also presented. Such data provide valuable insights into the basic phenomena involved in explosions.

R. S. Conti; M. Hertzberg; F. T. Duda; K. L. Cashdollar

1983-01-01T23:59:59.000Z

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


361

Development of NF3 Deposit Removal Technology for the Portsmouth Gaseous Diffusion Plant  

SciTech Connect

This paper summarizes the Battelle, Stoller, and WASTREN (BSW) team's efforts, to date, in support of the United States Department of Energy's plans to remove uranium and technetium deposits before decommissioning the Portsmouth Gaseous Diffusion Plant. The BSW team investigated nitrogen trifluoride (NF{sub 3}) as a safer yet effective alternative gaseous treatment to the chlorine trifluoride (ClF{sub 3})-elemental fluorine (F{sub 2}) treatment currently used to remove uranium and technetium deposits from the uranium enrichment cascade. Both ClF{sub 3} and F{sub 2} are highly reactive, toxic, and hazardous gases, while NF{sub 3}, although toxic [1], is no more harmful than moth balls [2]. BSW's laboratory thermo-analytical and laboratory-scale prototype studies with NF{sub 3} established that thermal NF{sub 3} can effectively remove likely and potential uranium (UO{sub 2}F{sub 2} and UF{sub 4}) and technetium deposits (a surrogate deposit material, TcO{sub 2}, and pertechnetates) by conversion to volatile compounds. Our engineering evaluations suggest that NF{sub 3}'s effectiveness could be enhanced by combining with a lesser concentration of ClF{sub 3}. BSW's and other's studies indicate compatibility with Portsmouth materials of construction (aluminum, copper, and nickel). (authors)

Scheele, R.D.; McNamara, B.K.; Rapko, B.M.; Edwards, M.K.; Kozelisky, A.E.; Daniel, R.C. [Battelle Pacific Northwest Division, PO Box 999, Battelle Blvd, Richland, Washington 99352 (United States); McSweeney, T.I.; Maharas, S.J.; Weaver, P.J.; Iwamasa, K.J. [Battelle Columbus Operations, 505 King Avenue, Columbus, Ohio 43201 (United States); Kefgen, R.B. [WASTREN, Inc., 1864 Shyville Road, Piketon, Ohio 45661 (United States)

2006-07-01T23:59:59.000Z

362

Atmospheric Trace Gases from the Carbon Dioxide Information Analysis Center (CDIAC)  

DOE Data Explorer (OSTI)

CDIAC products are indexed and searchable through a customized interface powered by ORNL's Mercury search engine. Products include numeric data packages, publications, trend data, atlases, models, etc. and can be searched for by subject area, keywords, authors, product numbers, time periods, collection sites, spatial references, etc. Some of the collections may also be included in the CDIAC publication, Trends Online: A Compendium of Global Change Data. Most data sets, many with numerous data files, are free to download from CDIAC's ftp area. The collections under the CDIAC heading of Atmospheric Trace Gases include: Atmospheric Carbon Dioxide, Atmospheric Methane, Atmospheric Carbon Monoxide, Atmospheric Hydrogen, Isotopes in Greenhouse Gases, Radionuclides, Aerosols, and Other Trace Gases.

363

In situ removal of contamination from soil  

DOE Patents (OSTI)

A process of remediation of cationic heavy metal contamination from soil utilizes gas phase manipulation to inhibit biodegradation of a chelating agent that is used in an electrokinesis process to remove the contamination. The process also uses further gas phase manipulation to stimulate biodegradation of the chelating agent after the contamination has been removed. The process ensures that the chelating agent is not attacked by bioorganisms in the soil prior to removal of the contamination, and that the chelating agent does not remain as a new contaminant after the process is completed. 5 figs.

Lindgren, E.R.; Brady, P.V.

1997-10-14T23:59:59.000Z

364

Influence of diesel acidification on dibenzothiophene removal: A new desulfurization practice  

Science Journals Connector (OSTI)

Abstract Commercial diesel is often loaded with organosulphur compounds including hard-to-remove dibenzothiophene DBT and other derivatives. Following uncommon and simple procedure, dibenzothiophene was selectively removed upon diesel acidification by acetic acid prior to activated carbon adsorption. Initially, competitive adsorption tests from synthetic fuel proved that dibenzothiophene is preferentially removed over di/tri and tetra-aromatic hydrocarbons upon fuel acidification by 5% (by vol.) acetic acid. The efficacy of the proposed method was further validated by removing dibenzothiophene from commercial diesel containing 2578 (15)mgkg?1. The removal of DBT from complex diesel has increased from 27% to 55% upon acidification by 5% acetic acid. Acidity value of the treated diesel is within the regulated limit giving more chance for the new procedure for practical applications.

Yahya S. Al-Degs; Mohammad A. Al-Ghouti

2015-01-01T23:59:59.000Z

365

Experimental design to optimise colour removal of diazo dye Congo Red using Zero-Valent Iron  

Science Journals Connector (OSTI)

Two types of zero-valent iron named Iron Powder (IP) and Iron Wool (IW) were used for colour removal of Congo Red (CR) dye from aqueous solution. Strong acidic condition (pH 2?3) favoured 99% colour removal with 2454-2485 mg/g of dye removal capacity by IP and IW. Decolourization of CR followed first order kinetics. At acidic pH, COD (Chemical Oxygen Demand) removal was 14-15% probably by adsorption by various oxidised iron species and at pH 7, it increased to 85%, due to co-precipitation by iron oxide products. IW was reused for three successive cycles without compromising colour removal efficiency of CR.

Animesh Debnath; Saswati Chakraborty

2013-01-01T23:59:59.000Z

366

Increasing the purity of additives  

Science Journals Connector (OSTI)

In the preparation of high-purity additives a low-temperature treatment with Galosha ... . In the preparation of high-purity sulfonate additives, a preliminary removal by settling of insoluble compounds must be...

A. L. Dol'berg

1969-06-01T23:59:59.000Z

367

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

368

Hungary HEU removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

removal | National Nuclear Security Administration removal | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > content > Four-Year Plan > Hungary HEU removal Hungary HEU removal Location Hungary United States 47° 11' 51.6336" N, 19° 41' 15" E See map: Google Maps Printer-friendly version Printer-friendly version Javascript is required to view this map.

369

Mexico HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Removal | National Nuclear Security Administration Removal | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > content > Four-Year Plan > Mexico HEU Removal Mexico HEU Removal Location Mexico United States 24° 24' 35.298" N, 102° 49' 55.3116" W See map: Google Maps Printer-friendly version Printer-friendly version Javascript is required to view this map.

370

Kazakhstan HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Kazakhstan HEU Removal | National Nuclear Security Administration Kazakhstan HEU Removal | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > content > Four-Year Plan > Kazakhstan HEU Removal Kazakhstan HEU Removal Location Kazakhstan United States 48° 59' 44.1492" N, 67° 3' 37.9692" E See map: Google Maps Printer-friendly version Printer-friendly version

371

Sweden Plutonium Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Sweden Plutonium Removal | National Nuclear Security Administration Sweden Plutonium Removal | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > content > Four-Year Plan > Sweden Plutonium Removal Sweden Plutonium Removal Location Sweden United States 62° 24' 4.4136" N, 15° 22' 51.096" E See map: Google Maps Printer-friendly version Printer-friendly version

372

Method of removing polychlorinated biphenyl from oil  

DOE Patents (OSTI)

Polychlorinated biphenyls are removed from oil by extracting the biphenyls into methanol. The mixture of methanol and extracted biphenyls is distilled to separate methanol therefrom, and the methanol is recycled for further use in extraction of biphenyls from oil.

Cook, G.T.; Holshouser, S.K.; Coleman, R.M.; Harless, C.E.; Whinnery, W.N. III

1982-03-17T23:59:59.000Z

373

Part removal of 3D printed parts  

E-Print Network (OSTI)

An experimental study was performed to understand the correlation between printing parameters in the FDM 3D printing process, and the force required to remove a part from the build platform of a 3D printing using a patent ...

Pea Doll, Mateo

2014-01-01T23:59:59.000Z

374

Turkey HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

Turkey HEU Removal | National Nuclear Security Administration Turkey HEU Removal | National Nuclear Security Administration Our Mission Managing the Stockpile Preventing Proliferation Powering the Nuclear Navy Emergency Response Recapitalizing Our Infrastructure Continuing Management Reform Countering Nuclear Terrorism About Us Our Programs Our History Who We Are Our Leadership Our Locations Budget Our Operations Media Room Congressional Testimony Fact Sheets Newsletters Press Releases Speeches Events Social Media Video Gallery Photo Gallery NNSA Archive Federal Employment Apply for Our Jobs Our Jobs Working at NNSA Blog Home > content > Four-Year Plan > Turkey HEU Removal Turkey HEU Removal Location Turkey United States 38° 26' 50.2044" N, 40° 15' 14.0616" E See map: Google Maps Printer-friendly version Printer-friendly version

375

Excitation spectrum and quasiparticles in quantum gases. A rigorous approach  

E-Print Network (OSTI)

This thesis is devoted to a rigorous study of interacting quantum gases. The main objects of interest are the closely related concepts of excitation spectrum and quasiparticles. The immediate motivation of this work is to propose a spectral point of view concerning these two concepts. In the first part of this thesis we discuss the concepts of excitation spectrum and quasiparticles. We provide an overview of physical motivations and based on that we propose a spectral and Hamiltonian-based approach towards these terms. Based on that, we formulate definitions and propositions related to these concepts. In the second part we recall the Bogoliubov and Hartree-Fock-Bogoliubov approximations, which in the physics literature are used to obtain the quasiparticle picture. We show how these two approaches fit into a universal scheme which allows us to arrive at a quasiparticle picture in a more general setup. This scheme is based on the minimization of Hamiltonians over the so-called Gaussian states. Its abstract formulation is the content of Beliaev's Theorem. In the last part we present a rigorous result concerning the justification of the Bogoliubov approximation. This justification employs the concept of the mean-field and infinite-volume limit. We show that for a large number of particles, a large volume and a sufficiently high density, the low-lying energy-momentum spectrum of the homogeneous Bose gas is well described by the Bogoliubov approximation. This result, which is formulated in the form of a theorem, can be seen as the main result of this thesis.

Marcin Napirkowski

2014-09-02T23:59:59.000Z

376

Disk Quota Increase Request  

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

Disk Disk Quota Increase Disk Quota Increase Request NERSC will consider reasonable requests for changes in disk space and inode limits. Please submit a request through the "Request Forms" section at the NERSC help portal. If you select "Hopper scratch directory" from the "File System" menu below, the quota value requested applies to the combined contents of $SCRATCH and $SCRATCH2. Please ask for the least amount of resources you need, since the sum of disk space and inodes allocated to users already exceeds system capacity. In other words, system resources would be exhausted before all users could use their existing quotas. You can find out the current quotas and usage of disk space and inodes for your home and scratch file systems with the myquota command. You can find

377

Laser removal of sludge from steam generators  

DOE Patents (OSTI)

A method of removing unwanted chemical deposits known as sludge from the metal surfaces of steam generators with laser energy is provided. Laser energy of a certain power density, of a critical wavelength and frequency, is intermittently focused on the sludge deposits to vaporize them so that the surfaces are cleaned without affecting the metal surface (sludge substrate). Fiberoptic tubes are utilized for laser beam transmission and beam direction. Fiberoptics are also utilized to monitor laser operation and sludge removal.

Nachbar, Henry D. (Ballston Lake, NY)

1990-01-01T23:59:59.000Z

378

Oil removal from water via adsorption  

E-Print Network (OSTI)

WILLIAM EDWARD JACOBS 1974 OIL REMOVAL FROM WATER VIA ADSORPTION A Thesis by WILLIAM EDWARD JACOBS Submitted to the Graduate College of Texas ASM University in partial fulfillment of the requirement for the degree of MASTER OF SCIENCE... December 1973 Major Subject: Civil Engineering OIL REMOVAL FROM WATER VIA ADSORPTION A Thesis by WILLIAM EDWARD JACOBS Approved as to style and content by: C airman of Committee ea o Department m er Member Memb December 1973 ABSTRACT Oil...

Jacobs, William Edward

2012-06-07T23:59:59.000Z

379

Geochemical Data on Waters, Gases, Scales, and Rocks from the Dixie Valley  

Open Energy Info (EERE)

Geochemical Data on Waters, Gases, Scales, and Rocks from the Dixie Valley Geochemical Data on Waters, Gases, Scales, and Rocks from the Dixie Valley Region, Nevada (1996-1999) Jump to: navigation, search OpenEI Reference LibraryAdd to library Report: Geochemical Data on Waters, Gases, Scales, and Rocks from the Dixie Valley Region, Nevada (1996-1999) Abstract This report tabulates an extensive geochemical database on waters, gases, scales,rocks, and hot-spring deposits from the Dixie Valley region, Nevada. The samples fromwhich the data were obtained were collected and analyzed during 1996 to 1999. Thesedata provide useful information for ongoing and future investigations on geothermalenergy, volcanism, ore deposits, environmental issues, and groundwater quality in thisregion. Authors Los Alamos National Laboratory and NM Published

380

Intensive Sampling Of Noble Gases In Fluids At Yellowstone- I, Early  

Open Energy Info (EERE)

Intensive Sampling Of Noble Gases In Fluids At Yellowstone- I, Early Intensive Sampling Of Noble Gases In Fluids At Yellowstone- I, Early Overview Of The Data, Regional Patterns Jump to: navigation, search GEOTHERMAL ENERGYGeothermal Home Journal Article: Intensive Sampling Of Noble Gases In Fluids At Yellowstone- I, Early Overview Of The Data, Regional Patterns Details Activities (1) Areas (1) Regions (0) Abstract: The Roving Automated Rare Gas Analysis (RARGA) lab of Berkeley's Physics Department was deployed in Yellowstone National Park for a 19 week period commencing in June, 1983. During this time 66 gas and water samples representing 19 different regions of hydrothermal activity within and around the Yellowstone caldera were analyzed on site. Routinely, the abundances of five stable noble gases and the isotopic compositions of He,

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


381

Clarifying the Roles of Greenhouse Gases and ENSO in Recent Global Warming through Their Prediction Performance  

Science Journals Connector (OSTI)

It is well known that natural external forcings and decadal-to-millennial variability drove changes in the climate system throughout the Holocene. Regarding recent times, attribution studies have shown that greenhouse gases (GHGs) determined the ...

Umberto Triacca; Antonello Pasini; Alessandro Attanasio; Alessandro Giovannelli; Marco Lippi

2014-10-01T23:59:59.000Z

382

Eddy covariance flux measurements of pollutant gases in urban Mexico City  

E-Print Network (OSTI)

Eddy covariance (EC) flux measurements of the atmosphere/surface exchange of gases over an urban area are a direct way to improve and evaluate emissions inventories, and, in turn, to better understand urban atmospheric ...

Velasco, Erik

383

Characteristic parameters of geigermller counter gases. Propane-argon and propane-helium mixtures  

Science Journals Connector (OSTI)

The combination of the Wilkinson and the Diethorn-Kohman expressions of counter operation was tested under conditions in which different rare gases were used with the same quench gas as Geiger-Mller counter f...

Richard G. Pannbacker; Robert W. Kiser

1962-02-01T23:59:59.000Z

384

Cosmogenic and trapped rare gases in Luna-24 drill core samples  

Science Journals Connector (OSTI)

The elemental and isotopic composition of noble gases in six samples from different depths of the Luna-24 drill core soil column, obtained by mass spectrometric analyses, are presented and the results are comp...

J. T. Padia; M. N. Rao; T. R. Venkatesan

1979-06-01T23:59:59.000Z

385

Adsorption Modeling of Coalbed Gases and the Effects of Water on Their Adsorption Behavior.  

E-Print Network (OSTI)

??The simplified local-density/Peng-Robinson (SLD-PR) adsorption model was utilized to investigate the adsorption behavior of coalbed gases on coals of varying rank. The model parameters were (more)

Mohammad, Sayeed Ahmed

2009-01-01T23:59:59.000Z

386

Quantifying emissions of greenhouse gases from South Asia through a targeted measurement campaign  

E-Print Network (OSTI)

Methane (CH 4 ), nitrous oxide (N20) and sulfur hexafluoride (SF6) are powerful greenhouse gases with global budgets that are well-known but regional distributions that are not adequately constrained for the purposes of ...

Ganesan, Anita Lakshmi

2013-01-01T23:59:59.000Z

387

Load Preheating Using Flue Gases from a Fuel-Fired Heating System  

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

This tip sheet discusses how the thermal efficiency of a process heating system can be improved significantly by using heat contained in furnace flue gases to preheat the furnace load.

388

Iron-based alloys with corrosion resistance to oxygen-sulfur mixed gases  

DOE Patents (OSTI)

An iron-based alloy with improved performance with exposure to oxygen-sulfur mixed gases with the alloy containing about 9--30 wt. % Cr and a small amount of Nb and/or Zr implanted on the surface of the alloy to diffuse a depth into the surface portion, with the alloy exhibiting corrosion resistance to the corrosive gases without bulk addition of Nb and/or Zr and without heat treatment at temperatures of 1000--1100 C. 7 figs.

Natesan, K.

1992-11-17T23:59:59.000Z

389

Iron-based alloys with corrosion resistance to oxygen-sulfur mixed gases  

DOE Patents (OSTI)

An iron-based alloy with improved performance with exposure to oxygen-sulfur mixed gases with the alloy containing about 9-30 wt. % Cr and a small amount of Nb and/or Zr implanted on the surface of the alloy to diffuse a depth into the surface portion, with the alloy exhibiting corrosion resistance to the corrosive gases without bulk addition of Nb and/or Zr and without heat treatment at temperatures of 1000.degree.-1100.degree. C.

Natesan, Krishnamurti (Naperville, IL)

1992-01-01T23:59:59.000Z

390

Factors affecting the recovery of petroleum in projects involving the injection of liquefied petroleum gases (LPG)  

E-Print Network (OSTI)

FACTORS AFFECTING THE RECOVERY OF PETROLEUM IN PROJECTS INVOLVING THE INJECTION OF LIQUEFIED PETROLEUM GASES (LPG) A Thesis By GERRY A. GRAHAM Submitted to the Graduate School of the Agricultural and Mechanical College of Texas in partial... fulfillment of the requirements for the degree of MASTER OF SCIENCE August, 1961 Major Subject: Petroleum Engineering GERRY A. GRAHAM FACTORS AFFECTING THE RECOVERY OF PETROLEUM IN PROJECTS INVOLVING THE INJECTION OF LIQUEFIED PETROLEUM GASES (LPG) A...

Graham, Gerry A

2012-06-07T23:59:59.000Z

391

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

392

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

393

Studies on steam condensation with non-condensable gases in a horizontal condenser tube for advanced nuclear reactors using RELAP5  

Science Journals Connector (OSTI)

Horizontal heat exchangers are used in advanced light water nuclear reactors in their passive cooling systems, such as Residual Heat Removal System (RHRS) and Passive Containment Cooling System (PCCS). Horizontal condensation studies of steam with non-condensable gases mixtures in these heat exchangers are very important. This work presents a comparison between simulation results and experimental data in steady state conditions for some inlet pressure, steam and non-condensable gases (air) inlet mass fractions. The test section was modelled and the simulations were performed with the RELAP5 code. Experimental tests were carried out for 200??400 kPa inlet pressure and 5%, 10%, 15% and 20% of inlet air mass fractions. Comparisons between experimental data and simulation results are presented for 200 kPa and 400 kPa pressure conditions and showed good agreement. New correlations for heat transfer coefficients in these steam-air conditions must be theoretically and experimentally studied and implemented in the RELAP5 code.

L.A. Macedo; W.M. Torres

2011-01-01T23:59:59.000Z

394

Removal of \\{PAHs\\} with surfactant-enhanced soil washing: Influencing factors and removal effectiveness  

Science Journals Connector (OSTI)

PAH removal with surfactant enhanced washing was investigated through a series of laboratory tests to examine the effect of stirring speed, washing time, surfactant concentration, liquid/solid ratio, temperature, and on-and-off mode. The first four factors show significant influence on the PAH removal while the latter two do not. Total removal ratio and a new proposed parameter, solubilization percentage, are used to evaluate the effectiveness quantitatively.

Sheng Peng; Wei Wu; Jiajun Chen

2011-01-01T23:59:59.000Z

395

What CO2 well gases tell us about the origin of noble gases in the mantle and their relationship to the atmosphere  

Science Journals Connector (OSTI)

...mantle-rich CO2 well gases, with samples lying on the air-solar mixing line. The most solar-rich gas, from Bravo Dome in New Mexico, had a 10 per cent excess above air value. Since solar and Q-Xe are so similar in composition, it is not possible...

2008-01-01T23:59:59.000Z

396

Fast non-explosive gases for drift chambers  

SciTech Connect

Typical gases which are stock at Fermilab are Ar:C/sub 2/H/sub 6/(50:50) and Ar:CO/sub 2/ (80:20). Argon:Ethane has the virtue of high gas gain and a saturated drift velocity. In fact, parametrizing the drift velocity as a function of electric field we find v/sub d/(E) = v/sub o/(1/minus/e/sup -E/E/o) with v/sub o/ approx. = 5.4 cm/..mu..sec and E/sub o/ = 160 V/cm. However, safety considerations make this gas somewhat inconvenient. The addition of alcohol as quencher also raises the saturation field to, for example, E/sub o/ approx. = 500 V/cm for 1.5% added alcohol. This gas also tends to break up in a high-beam flux environment and leave carbon deposits. The addition of alcohol to avoid such aging often takes a unit cell out of saturation over its entire volume. Finally, for collider applications it is useful to exclude free protons from the gas in order to reduce the sensitivity to the sea of slow neutrons which are present in the collider environment. In contrast, Ar:CO/sub 2/ (80:20) is a gas with more moderate gas gain. The drift velocity at high field is v/sub d/(E > 1.5 kV/cm) approx. = 5.8 cm/..mu..sec. For most field configurations this gas does not saturate, causing a long tail in the drift time distrubtion due to low field regions in the unit cell. The virtues of this gas mixture are that it is cheap, not flammable, and stable under high-beam flux. However as the Collider Upgrade progresses, we wish to find a gas which is faster than 5.0 cm/..mu..sec since the time separation between collisions will at some point be less than drift time of 1..mu..sec for drift distance of 5 cm. 3 refs., 5 figs.

Green, D.; Haggerty, H.; Oshima, N.; Yamada, R.

1988-05-01T23:59:59.000Z

397

A Theory of the Electric Discharge Through Gases  

Science Journals Connector (OSTI)

Three general differential equations are set up which determine the average behavior of a discharge of electricity through a gas. Approximate solutions, giving the electric field E and the concentration of electrons and positive ions, n1 and n2, at any distance x from the cathode, are found for several ranges of value of E.When E is large, the solution corresponds to the conditions in the cathode and anode fall spaces in a glow discharge. Equations are obtained for the potential drop V across the fall space; the current density at the electrode divided by the square of the gas pressure, jp2; and the thickness of the fall space times the pressure, pd.These equations indicate that for the cathode fall space there is a certain minimum value of V, called Vn; and for jp2, called jnp2; and a corresponding maximum value of pd, pdn, beyond which values the discharge ceases. These stationary values are shown to be constants, dependent only on the nature of the gas used and of the cathode material, and correspond to the normal cathode fall space. The equation determining Vn is shown to be of the right from by comparison with the experimentally determined values. From these values of Vn, values of jnp2 and of pdn are calculated for four gases and four cathode materials, and the calculated values check with the experimental data. The corresponding equations for the anode fall space show why there is no corresponding normal anode fall.A consideration of the discharge when E is large throughout the distance between electrodes indicates that there is another stationary value of the cathode fall space when the current density at the cathode reaches its maximum possible value. The V in this case is much smaller than the Vn for the glow discharge, and the form of the equations indicate that they describe the conditions in an electric arc.Another approximate equation is obtained when E is constant, which is the case in the positive column of a glow discharge. This solution indicates that within certain limits of pressure and current density, small sinusoidal variations about the average value Ep, are possible in E. These correspond to the striations sometimes observed in the positive column. The equations determining Ep and those determining the distance between striations check with the known empirical laws relating these amounts to the pressure, the radius of the discharge tube and the critical potentials of the gas used. A general discussion is given of the Faraday dark space and reasons are given why it should be near the cathode rather than the anode.

Philip M. Morse

1928-06-01T23:59:59.000Z

398

PHASE BEHAVIOR OF LIGHT GASES IN HYDROCARBON AND AQUEOUS SOLVENTS  

SciTech Connect

Under previous support from the Department of Energy, an experimental facility has been established and operated to measure valuable vapor-liquid equilibrium data for systems of interest in the production and processing of coal fluids. To facilitate the development and testing of models for prediction of the phase behavior for such systems, we have acquired substantial amounts of data on the equilibrium phase compositions for binary mixtures of heavy hydrocarbon solvents with a variety of supercritical solutes, including hydrogen, methane, ethane, carbon monoxide, and carbon dioxide. The present project focuses on measuring the phase behavior of light gases and water in Fischer-Tropsch (F-T) type solvents at conditions encountered in indirect liquefaction processes and evaluating and developing theoretically-based correlating frameworks to predict the phase behavior of such systems. Specific goals of the proposed work include (a) developing a state-of-the-art experimental facility to permit highly accurate measurements of equilibrium phase compositions (solubilities) of challenging F-T systems, (b) measuring these properties for systematically-selected binary, ternary and molten F-T wax mixtures to provide critically needed input data for correlation development, (c) developing and testing models suitable for describing the phase behavior of such mixtures, and (d) presenting the modeling results in generalized, practical formats suitable for use in process engineering calculations. During the present period, the Park-Gasem-Robinson (PGR) equation of state (EOS) has been modified to improve its volumetric and equilibrium predictions. Specifically, the attractive term of the PGR equation was modified to enhance the flexibility of the model, and a new expression was developed for the temperature dependence of the attractive term in this segment-segment interaction model. The predictive capability of the modified PGR EOS for vapor pressure, and saturated liquid and vapor densities was evaluated for selected normal paraffins, normal alkenes, cyclo-paraffins, light aromatics, argon, carbon dioxide and water. The generalized EOS constants and substance-specific characteristic parameters in the modified PGR EOS were obtained from the pure component vapor pressures, and saturated liquid and vapor molar volumes. The calculated phase properties were compared to those of the Peng-Robinson (PR), the simplified-perturbed-hard-chain theory (SPHCT) and the original PGR equations. Generally, the performance of the proposed EOS was better than the PR, SPHCT and original PGR equations in predicting the pure fluid properties (%AAD of 1.3, 2.8 and 3.7 for vapor pressure, saturated liquid and vapor densities, respectively).

KHALED A.M. GASEM; ROBERT L. ROBINSON, JR.

1998-08-31T23:59:59.000Z

399

The Effect of Flow Rate of Very Dilute Sulfuric Acid on Xylan, Lignin, and Total Mass Removal from Corn Stover  

E-Print Network (OSTI)

The Effect of Flow Rate of Very Dilute Sulfuric Acid on Xylan, Lignin, and Total Mass Removal from mass, xylan, and lignin and increases cellulose digestibility compared to batch operations at otherwise in corn stover at 180 °C. A flow rate of 10 mL/min in a 3.8-mL reactor enhanced xylan removal by about 25

California at Riverside, University of

400

Influence of processing gases on the properties of cold atmospheric plasma SiOxCy coatings  

Science Journals Connector (OSTI)

Abstract Thin layers of SiOxCy (y=4?x and 3?x?4) were applied using a cold atmospheric plasma torch on glass substrates. The aim was to investigate using Atomic Force Microscopy (AFM), X-ray photoelectron spectroscopy (XPS) and time-of-flight secondary ion mass spectrometry (Tof-Sims) the influence of the gases used on the morphology and composition of the deposits. A hexamethyldisilane (HMDS) precursor was injected in post-discharge in an air or nitrogen plasma using a carrier gas (air or nitrogen) and was applied on the substrate previously pre-treated by an air or nitrogen plasma. The carrier gas and plasma gas flows and the distance between the substrate and the plasma torch, the scanning speed, and the precursor flows were kept constant during the study. The gas used during activation pre-treatment showed no particular influence on the characteristics of the deposit. When air is used both as plasma and carrier gas, the coating layer is thicker (96nm) than when nitrogen is used (64nm). It was also evidenced that the gas carrying the precursor has little influence on the hydrophobicity of the coating, contrary to the plasma gas. The latter significantly influences the surface characteristics of the coatings. When air is used as plasma gas, a compact coating layer is obtained and the surface has a water contact angle (WCA) of 82. When nitrogen is used, the deposit is more hydrophobic (WCA of 100) and the deposit morphology is different. This increase in hydrophobicity could be correlated to the increase of SiOC bonds in the upper surface layers evidenced by XPS analyzes. This observation was then confirmed by Tof-Sims analyzes carried out on these thin layers. A uniform distribution of Carbons in the siloxane coating could also be observed using Tof-Sims 2D reconstruction images of cross sections of the deposited layers.

H. Hamze; M. Jimenez; D. Deresmes; A. Beaurain; N. Nuns; M. Traisnel

2014-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "gases removed increased" from the National Library of EnergyBeta (NLEBeta).
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401

Evaluation of Passive and Active Soot Filters for Removal of...  

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

Passive and Active Soot Filters for Removal of Particulate Emissions from Diesel Engines Evaluation of Passive and Active Soot Filters for Removal of Particulate Emissions from...

402

High Metal Removal Rate Process for Machining Difficult Materials...  

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

High Metal Removal Rate Process for Machining Difficult Materials High Metal Removal Rate Process for Machining Difficult Materials highmetalremovalprocessfactsheet.pdf More...

403

Oak Ridge Removes Laboratory's Greatest Source of Groundwater...  

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

Removes Laboratory's Greatest Source of Groundwater Contamination Oak Ridge Removes Laboratory's Greatest Source of Groundwater Contamination May 1, 2012 - 12:00pm Addthis Workers...

404

Vehicle Technologies Office Merit Review 2014: Removing Barriers...  

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

Review 2014: Removing Barriers, Implementing Policies and Advancing Alternative Fuels Markets in New England Vehicle Technologies Office Merit Review 2014: Removing Barriers,...

405

Advanced Water Removal via Membrane Solvent Extraction | Department...  

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

Water Removal via Membrane Solvent Extraction Advanced Water Removal via Membrane Solvent Extraction advwaterremovalmse.pdf More Documents & Publications Advance Patent Waiver...

406

NITROGEN REMOVAL FROM NATURAL GAS  

SciTech Connect

The objective of this project was to develop a membrane process for the denitrogenation of natural gas. Large proven reserves in the Lower-48 states cannot be produced because of the presence of nitrogen. To exploit these reserves, cost-effective, simple technology able to reduce the nitrogen content of the gas to 4-5% is required. Technology applicable to treatment of small gas streams (below 10 MMscfd) is particularly needed. In this project membranes that selectively permeate methane and reject nitrogen in the gas were developed. Preliminary calculations show that a membrane with a methane/nitrogen selectivity of 3 to 5 is required to make the process economically viable. A number of polymer materials likely to have the required selectivities were evaluated as composite membranes. Polyacetylenes such as poly(1-trimethylsilyl-1-propyne) [PTMSP] and poly(4-methyl-2-pentyne) [PMP] had high selectivities and fluxes, but membranes prepared from these polymers were not stable, showing decreasing flux and selectivity during tests lasting only a few hours. Parel, a poly(propylene oxide allyl glycidyl ether) had a selectivity of 3 at ambient temperatures and 4 or more at temperatures of {minus}20 C. However, Parel is no longer commercially available, and we were unable to find an equivalent material in the time available. Therefore, most of our experimental work focused on silicone rubber membranes, which have a selectivity of 2.5 at ambient temperatures, increasing to 3-4 at low temperatures. Silicone rubber composite membranes were evaluated in bench-scale module tests and with commercial-scale, 4-inch-diameter modules in a small pilot plant. Over six days of continuous operation at a feed gas temperature of {minus}5 to {minus}10 C, the membrane maintained a methane/nitrogen selectivity of about 3.3. Based on the pilot plant performance data, an analysis of the economic potential of the process was prepared. We conclude that a stand-alone membrane process is the lowest-cost technology for small gas streams containing less than 10% nitrogen. The membrane process can recover more than 60-70% of the hydrocarbon content of the gas at a cost of $0.60-0.70/Mscfd. The capital cost of the process is about $100-200/Mscf. A number of small operators appear to be ready to use the technology if these costs can be demonstrated in the field. A second, and perhaps better, application of the technology is to combine the membrane process with a cryogenic process to treat large gas streams containing 10-20% nitrogen. The combination process achieves significant synergies. The membrane process performs a bulk separation of the gas, after which the cryogenic process treats the membrane residue (nitrogen-enriched) gas to recover more methane. Overall, hydrocarbon recoveries are greater than 95%. The capital cost of the combination process is lower than that of either process used alone and the processing costs are in the range $0.30-0.40/Mscf. This operating cost would be attractive to many gas producers. MTR is collaborating with a producer of cryogenic systems to further develop the combination process. A number of innovations in membrane process designs were made during the project; four U.S. patents covering various aspects of the technology were filed and issued.

K.A. Lokhandwala; M.B. Ringer; T.T. Su; Z. He; I. Pinnau; J.G. Wijmans; A. Morisato; K. Amo; A. DaCosta; R.W. Baker; R. Olsen; H. Hassani; T. Rathkamp

1999-12-31T23:59:59.000Z

407

241-AZ-101 pump removal trough analysis  

SciTech Connect

As part of the current Hanford mission of environmental cleanup, various long length equipment must be removed from highly radioactive waste tanks. The removal of equipment will utilize portions of the Equipment Removal System for Project W320 (ERS-W320), specifically the 50 ton hydraulic trailer system. Because the ERS-W320 system was designed to accommodate much heavier equipment it is adequate to support the dead weight of the trough, carriage and related equipment for 241AZ101 pump removal project. However, the ERS-W320 components when combined with the trough and its` related components must also be analyzed for overturning due to wind loads. Two troughs were designed, one for the 20 in. diameter carriage and one for the 36 in. diameter carriage. A proposed 52 in. trough was not designed and, therefore is not included in this document. In order to fit in the ERS-W320 strongback the troughs were design with the same widths. Structurally, the only difference between the two troughs is that more material was removed from the stiffener plates on the 36 in trough. The reduction in stiffener plate material reduces the allowable load. Therefore, only the 36 in. trough was analyzed.

Coverdell, B.L.

1995-10-17T23:59:59.000Z

408

Biochemical Removal of HAP Precursors from Coal  

SciTech Connect

Column biooxidation tests with Kentucky coal confirmed results of earlier shake flask tests showing significant removal from the coal of arsenic, selenium, cobalt, manganese, nickel and cadmium. Rates of pyrite biooxidation in Kentucky coal were only slightly more than half the rates found previously for Indiana and Pittsburgh coals. Removal of pyrite from Pittsburgh coal by ferric ion oxidation slows markedly as ferrous ions accumulate in solution, requiring maintenance of high redox potentials in processes designed for removal of pyrite and hazardous air pollutant (HAP) precursors by circulation of ferric solutions through coal. The pyrite oxidation rates obtained in these tests were used by Unifield Engineering to support the conceptual designs for alternative pyrite and HAP precursor bioleaching processes for the phase 2 pilot plant. Thermophilic microorganisms were tested to determine if mercury could be mobilized from coal under elevated growth temperatures. There was no evidence for mercury removal from coal under these conditions. However, the activity of the organisms may have liberated mercury physically. It is also possible that the organisms dissolved mercury and it readsorbed to the clay preferentially. Both of these possibilities are undergoing further testing. The Idaho National Engineering and Environmental Laboratory?s (INEEL) slurry column reactor was operated and several batches of feed coal, product coal, waste solids and leach solutions were submitted to LBL for HAP precursor analysis. Results to date indicate significant removal of mercury, arsenic and other HAP precursors in the combined physical-biological process.

Gregory J. Olson

1997-05-12T23:59:59.000Z

409

Increasing efficiency, reducing emissions with hydrous ethanol in diesel engines  

E-Print Network (OSTI)

Increasing efficiency, reducing emissions with hydrous ethanol in diesel engines Ethanol continuedOber 2013 Catalystcts.umn.edu Nearly all corn-based ethanol produced in the United States is anhydrous processes required to remove the water from ethanol consume a great deal of energy. Researchers from

Minnesota, University of

410

ORIGINAL PAPER Litter legacy increases the competitive advantage of invasive  

E-Print Network (OSTI)

ORIGINAL PAPER Litter legacy increases the competitive advantage of invasive Phragmites australis monospecific dominance has rarely been investigated. We used stands of the common reed, Phragmites australis positioned on Phragmites expansion fronts, we removed litter to isolate its effect from live Phragmites

Bertness, Mark D.

411

A high-speed photoresist removal process using multibubble microwave plasma under a mixture of multiphase plasma environment  

SciTech Connect

This paper proposes a photoresist removal process that uses multibubble microwave plasma produced in ultrapure water. A non-implanted photoresist and various kinds of ion-implanted photoresists such as B, P, and As were treated with a high ion dose of 5 10{sup 15} atoms/cm{sup 2} at an acceleration energy of 70 keV; this resulted in fast removal rates of more than 1 ?m/min. When the distance between multibubble microwave plasma and the photoresist film was increased by a few millimeters, the photoresist removal rates drastically decreased; this suggests that short-lived radicals such as OH affect high-speed photoresist removal.

Ishijima, Tatsuo [Research Center for Sustainable Energy and Technology, Kanazawa University, Kakuma-machi, Kanazawa, Ishikawa 920-1192 (Japan)] [Research Center for Sustainable Energy and Technology, Kanazawa University, Kakuma-machi, Kanazawa, Ishikawa 920-1192 (Japan); Nosaka, Kohei [Graduate School of Natural Science and Technology, Kanazawa University, Kakuma-machi, Kanazawa, Ishikawa 920-1192 (Japan)] [Graduate School of Natural Science and Technology, Kanazawa University, Kakuma-machi, Kanazawa, Ishikawa 920-1192 (Japan); Tanaka, Yasunori; Uesugi, Yoshihiko [Research Center for Sustainable Energy and Technology, Kanazawa University, Kakuma-machi, Kanazawa, Ishikawa 920-1192 (Japan) [Research Center for Sustainable Energy and Technology, Kanazawa University, Kakuma-machi, Kanazawa, Ishikawa 920-1192 (Japan); Graduate School of Natural Science and Technology, Kanazawa University, Kakuma-machi, Kanazawa, Ishikawa 920-1192 (Japan); Goto, Yousuke; Horibe, Hideo [Department of Applied Chemistry, Kanazawa Institute of Technology, 3-1 Yatsukaho, Hakusan, Ishikawa 924-0838 (Japan)] [Department of Applied Chemistry, Kanazawa Institute of Technology, 3-1 Yatsukaho, Hakusan, Ishikawa 924-0838 (Japan)

2013-09-30T23:59:59.000Z

412

Method for removing cesium from a nuclear reactor coolant  

DOE Patents (OSTI)

A method of and system for removing cesium from a liquid metal reactor coolant including a carbon packing trap in the primary coolant system for absorbing a major portion of the radioactive cesium from the coolant flowing therethrough at a reduced temperature. A regeneration subloop system having a secondary carbon packing trap is selectively connected to the primary system for isolating the main trap therefrom and connecting it to the regeneration system. Increasing the temperature of the sodium flowing through the primary trap diffuses a portion of the cesium

Colburn, Richard P. (Pasco, WA)

1986-01-01T23:59:59.000Z

413

Removal of Oil from Water by Inverse Fluidization of Aerogels  

Science Journals Connector (OSTI)

On the contrary, filtration carried out using packed beds of granular materials has the following disadvantages: pressure drop increases proportionally to the flow rate, and the bed voidage reduces as the filter saturates with the contaminants. ... The water flow exits from the bottom of the column and passes through a Keystone Sediment Filter (model 2323N) in order to remove any entrained aerogel granules before being discarded. ... the emulsion was passed through the filters until satn. of the filter was indicated by the appearance of oil in the filtrate (breakthrough). ...

Jose A. Quevedo; Gaurav Patel; Robert Pfeffer

2008-08-16T23:59:59.000Z

414

Impact of plant assemblages on nutrient removal in constructed wetlands  

Science Journals Connector (OSTI)

Four different mesocosm scale constructed wetlands - monoculture (Carexstipata), self-designed (passive) community, mixed planted monoculture-passive community and a non-vegetated control - were compared to assess the effects of plant community composition on the removal of inorganic nutrients from agricultural runoff (synthetic tile water). The mixed and self-designed systems consistently produced effluent NO3-N concentrations significantly below 10 mg/L, and had higher rates of evapotranspiration. Results indicate the type and composition of the plant community can impact the performance of constructed wetlands. Therefore, self-design of the plant community through the existing seed bank may increase the effectiveness of wetlands in treating agricultural runoff.

III">Ralph E. Spayd III; Shirley E. Clark; Katherine H. Baker

2013-01-01T23:59:59.000Z

415

Collisions of the Second Kind and their Effect on the Field in the Positive Column of a Glow Discharge in Mixtures of the Rare Gases  

Science Journals Connector (OSTI)

A study was made of the collision processes in the uniform positive column of a glow discharge in mixtures composed of two of the rare gases, helium, neon and argon and a mixture of each of these gases with mercury vapor, by means of measurements of the electric field and by spectroscopic observations. The discharge tube was of cylindrical form, 4.4 cm in diameter, with plane parallel electrodes The electrode distance could be varied from zero to 32 cm by means of an external electromagnet. The phenomena were studied with currents from 20 to 40 m.a. and pressures from 5 to 30 mm of mercury. The mixtures were circulated through the discharge tube and a purifying system during the entire time that observations were being made. It was very important to maintain extreme purity of the gases. The results show that the electrical and spectral characteristics of the uniform positive column in mixtures of monatomic gases can be explained principally in terms of collisions of the second kind between the ions or metastable atoms of one gas and the neutral atoms of the other. The effect of limitation of electron velocities is insufficient to explain the results, and its effect is shown to be negligible as compared with collisions of the second kind when the concentration of one gas is very small. The necessary condition for a large effect to be produced in the electrical and spectral characteristics of the positive column by a small percentage of one gas added to another is that a close resonance exists between the metastable states of the main gas and the ionization potential or excited states of the added gas atom or ion. By the introduction of as little as 0.4 percent neon or argon into helium, a marked increase in the electric field is produced, and the spectrum emitted is changed almost completely from the arc spectrum of helium to that of neon or argon respectively. The addition of mercury vapor at room temperature to neon caused a decrease of 45 percent in the field while the addition of mercury to either argon or helium produced a small increase. In the cases where the excitation and ionization potentials of the added gas were above the metastable states of the main gas, no reactions between the two gases could occur to affect the concentration of metastable atoms. In these cases practically no change in either the spectral or electrical characteristics were observed upon adding a small amount of one gas to another. However, in larger proportions the change produced in the field was proportional to the amounts of the two gases and the difference between the field in each of the pure gases. This result is accounted for mainly by the difference in the energy of the ionization processes in the two gases by electron impact.

L. B. Headrick and O. S. Duffendack

1931-03-15T23:59:59.000Z

416

Gas transport properties of reverse-selective poly(ether-b-amide6)/[Emim][BF4] gel membranes for CO2/light gases separation  

Science Journals Connector (OSTI)

Abstract The present research investigates deeply effect of 1-ethyl-3 methylimidazolium tetrafluoroborate ([Emim][BF4]) ionic liquid on separation performance and transport properties of poly(ether-b-amide6)(Pebax1657) at different operating pressures from 2 to 20 bar and temperatures from 25 to 65C. [Emim][BF4] showed interesting separation factor for CO2/light gases as a solvent and it was expected that its addition to Pebax1657 leads more amorphous structure, thereby diffusion and permeability of gases increase. [Emim][BF4] was added to the polymer solution up to 100 wt.% of Pebax1657 weight and permeation coefficients of CO2, H2, CH4 and N2 through the prepared membranes were measured. The results showed remarkable increment in permeation of all the tested gases, particularly CO2 and ideal selectivity of CO2/H2 enhanced significantly due to high solubility selectivity of the added compound. Effect of operating conditions on solubility coefficients were also investigated, thus sorption isotherms and activation energies of permeability, solubility and diffusion were calculated. In addition, the membranes were characterized by SEM, DSC, FT-IR spectroscopy and Tensile analysis to inspect changes in their physical and thermal properties, precisely.

Hesamoddin Rabiee; Ali Ghadimi; Toraj Mohammadi

2014-01-01T23:59:59.000Z

417

A BIOMASS-BASED MODEL TO ESTIMATE THE PLAUSIBILITY OF EXOPLANET BIOSIGNATURE GASES  

SciTech Connect

Biosignature gas detection is one of the ultimate future goals for exoplanet atmosphere studies. We have created a framework for linking biosignature gas detectability to biomass estimates, including atmospheric photochemistry and biological thermodynamics. The new framework is intended to liberate predictive atmosphere models from requiring fixed, Earth-like biosignature gas source fluxes. New biosignature gases can be considered with a check that the biomass estimate is physically plausible. We have validated the models on terrestrial production of NO, H{sub 2}S, CH{sub 4}, CH{sub 3}Cl, and DMS. We have applied the models to propose NH{sub 3} as a biosignature gas on a 'cold Haber World', a planet with a N{sub 2}-H{sub 2} atmosphere, and to demonstrate why gases such as CH{sub 3}Cl must have too large of a biomass to be a plausible biosignature gas on planets with Earth or early-Earth-like atmospheres orbiting a Sun-like star. To construct the biomass models, we developed a functional classification of biosignature gases, and found that gases (such as CH{sub 4}, H{sub 2}S, and N{sub 2}O) produced from life that extracts energy from chemical potential energy gradients will always have false positives because geochemistry has the same gases to work with as life does, and gases (such as DMS and CH{sub 3}Cl) produced for secondary metabolic reasons are far less likely to have false positives but because of their highly specialized origin are more likely to be produced in small quantities. The biomass model estimates are valid to one or two orders of magnitude; the goal is an independent approach to testing whether a biosignature gas is plausible rather than a precise quantification of atmospheric biosignature gases and their corresponding biomasses.

Seager, S.; Bains, W.; Hu, R. [Department of Earth, Atmospheric, and Planetary Sciences, Massachusetts Institute of Technology, 77 Massachusetts Ave., Cambridge, MA 02139 (United States)

2013-10-01T23:59:59.000Z

418

A Biomass-based Model to Estimate the Plausibility of Exoplanet Biosignature Gases  

Science Journals Connector (OSTI)

Biosignature gas detection is one of the ultimate future goals for exoplanet atmosphere studies. We have created a framework for linking biosignature gas detectability to biomass estimates, including atmospheric photochemistry and biological thermodynamics. The new framework is intended to liberate predictive atmosphere models from requiring fixed, Earth-like biosignature gas source fluxes. New biosignature gases can be considered with a check that the biomass estimate is physically plausible. We have validated the models on terrestrial production of NO, H2S, CH4, CH3Cl, and DMS. We have applied the models to propose NH3 as a biosignature gas on a "cold Haber World," a planet with a N2-H2 atmosphere, and to demonstrate why gases such as CH3Cl must have too large of a biomass to be a plausible biosignature gas on planets with Earth or early-Earth-like atmospheres orbiting a Sun-like star. To construct the biomass models, we developed a functional classification of biosignature gases, and found that gases (such as CH4, H2S, and N2O) produced from life that extracts energy from chemical potential energy gradients will always have false positives because geochemistry has the same gases to work with as life does, and gases (such as DMS and CH3Cl) produced for secondary metabolic reasons are far less likely to have false positives but because of their highly specialized origin are more likely to be produced in small quantities. The biomass model estimates are valid to one or two orders of magnitude; the goal is an independent approach to testing whether a biosignature gas is plausible rather than a precise quantification of atmospheric biosignature gases and their corresponding biomasses.

S. Seager; W. Bains; R. Hu

2013-01-01T23:59:59.000Z

419

Waste Heat Recovery from High Temperature Off-Gases from Electric Arc Furnace  

SciTech Connect

This article presents a study and review of available waste heat in high temperature Electric Arc Furnace (EAF) off gases and heat recovery techniques/methods from these gases. It gives details of the quality and quantity of the sensible and chemical waste heat in typical EAF off gases, energy savings potential by recovering part of this heat, a comprehensive review of currently used waste heat recovery methods and potential for use of advanced designs to achieve a much higher level of heat recovery including scrap preheating, steam production and electric power generation. Based on our preliminary analysis, currently, for all electric arc furnaces used in the US steel industry, the energy savings potential is equivalent to approximately 31 trillion Btu per year or 32.7 peta Joules per year (approximately $182 million US dollars/year). This article describes the EAF off-gas enthalpy model developed at Oak Ridge National Laboratory (ORNL) to calculate available and recoverable heat energy for a given stream of exhaust gases coming out of one or multiple EAF furnaces. This Excel based model calculates sensible and chemical enthalpy of the EAF off-gases during tap to tap time accounting for variation in quantity and quality of off gases. The model can be used to estimate energy saved through scrap preheating and other possible uses such as steam generation and electric power generation using off gas waste heat. This article includes a review of the historical development of existing waste heat recovery methods, their operations, and advantages/limitations of these methods. This paper also describes a program to develop and test advanced concepts for scrap preheating, steam production and electricity generation through use of waste heat recovery from the chemical and sensible heat contained in the EAF off gases with addition of minimum amount of dilution or cooling air upstream of pollution control equipment such as bag houses.

Nimbalkar, Sachin U [ORNL; Thekdi, Arvind [E3M Inc; Keiser, James R [ORNL; Storey, John Morse [ORNL

2014-01-01T23:59:59.000Z

420

Method of making thermally removable polyurethanes  

DOE Patents (OSTI)

A method of making a thermally-removable polyurethane material by heating a mixture of a maleimide compound and a furan compound, and introducing alcohol and isocyanate functional groups, where the alcohol group and the isocyanate group reacts to form the urethane linkages and the furan compound and the maleimide compound react to form the thermally weak Diels-Alder adducts that are incorporated into the backbone of the urethane linkages during the formation of the polyurethane material at temperatures from above room temperature to less than approximately 90.degree. C. The polyurethane material can be easily removed within approximately an hour by heating to temperatures greater than approximately 90.degree. C. in a polar solvent. The polyurethane material can be used in protecting electronic components that may require subsequent removal of the solid material for component repair, modification or quality control.

Loy, Douglas A. (Albuquerque, NM); Wheeler, David R. (Albuquerque, NM); McElhanon, James R. (Livermore, CA); Saunders, Randall S. (late of Albuquerque, NM); Durbin-Voss, Marvie Lou (Albuquerque, NM)

2002-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "gases removed increased" 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

Purifying rotary kiln waste gases in chamotte burning  

Science Journals Connector (OSTI)

A study of the operation of electric filters connected to rotary kilns for burning clay into chamotte showed that to increase the dust extraction efficiency it is necessary: with dust concentrations in the gas...

Yu. I. Chander; S. Z. Belinskii; L. G. Borisovskii

422

PHASE BEHAVIOR OF LIGHT GASES IN HYDROGEN AND AQUEOUS SOLVENTS  

SciTech Connect

Under previous support from the US Department of Energy, an experimental facility has been established and operated to measure valuable vapor-liquid equilibrium data for systems of interest in the production and processing of coal fluids. To facilitate the development and testing of models for prediction of the phase behavior for such systems, we have acquired substantial amounts of data on the equilibrium phase compositions for binary mixtures of heavy hydrocarbon solvents with a variety of supercritical solutes, including hydrogen, methane, ethane, carbon monoxide, and carbon dioxide. The present project focuses on measuring the phase behavior of light gases and water in Fischer-Tropsch (F-T) type solvents at conditions encountered in indirect liquefaction processes and evaluating and developing theoretically-based correlating frameworks to predict the phase behavior of such systems. Specific goals of the proposed work include (a) developing a state-of-the-art experimental facility to permit highly accurate measurements of equilibrium phase compositions (solubilities) of challenging F-T systems, (b) measuring these properties for systematically-selected binary, ternary and molten F-T wax mixtures to provide critically needed input data for correlation development, (c) developing and testing models suitable for describing the phase behavior of such mixtures, and (d) presenting the modeling results in generalized, practical formats suitable for use in process engineering calculations. During the present reporting period, the solubilities of hydrogen in n-hexane, carbon monoxide in cyclohexane, and nitrogen in phenanthrene and pyrene were measured using a static equilibrium cell over the temperature range from 344.3 to 433.2 K and pressures to 22.8 MPa. The uncertainty in these new solubility measurements is estimated to be less than 0.001 in mole fraction. The data were analyzed using the Peng-Robinson (PR) equation of state (EOS). In general, the PR EOS represents the experimental data well when a single interaction parameter (C{sub ij}) is used for each isotherm. In addition, the predictive capability of the modified Park-Gasem-Robinson (PGR) equation of state (EOS) was evaluated for selected carbon dioxide + normal paraffins, ethane + normal paraffins, and hydrogen + normal paraffins. A set of mixing rules was proposed for the modified EOS to extend its predictive capabilities to mixtures. The predicted bubble point pressures for the ethane + n-paraffin and carbon dioxide + n-paraffin binaries were compared to those of the Peng-Robinson (PR), simplified-perturbed-hard-chain theory (SPHCT) and original PGR equations. The predictive capability of the proposed equation is better or comparable to the PR, SPHCT and original PGR equations of state for the ethane binaries (%AAD of 1.9) and carbon dioxide binaries (%AAD of 2.0). For the hydrogen binaries, the modified PGR EOS showed much better performance (%AAD of 1.7) than the original PGR equation and comparable to the PR equation.

KHALED A.M. GASEM; ROBERT L. ROBINSON, JR.

1999-03-31T23:59:59.000Z

423

Phase Behavior of Light Gases in Hydrocarbon and Aqueous Solvents  

SciTech Connect

Under previous support from the Department of Energy, an experimental facility has been established and operated to measure valuable vapor-liquid equilibrium data for systems of interest in the production and processing of coal fluids. To facilitate the development and testing of models for prediction of the phase behavior for such systems, we have acquired substantial amounts of data on the equilibrium phase compositions for binary mixtures of heavy hydrocarbon solvents with a variety of supercritical solutes, including hydrogen, methane, ethane, carbon monoxide, and carbon dioxide. The present project focuses on measuring the phase behavior of light gases and water in Fischer-Tropsch (F-T) type solvents at conditions encountered in indirect liquefaction processes and evaluating and developing theoretically-based correlating frameworks to predict the phase behavior of such systems. Specific goals of the proposed work include (a) developing a state-of-the-art experimental facility to permit highly accurate measurements of equilibrium phase compositions (solubilities) of challenging F-T systems, (b) measuring these properties for systematically-selected binary, ternary and molten F-T wax mixtures to provide critically needed input data for correlation development, (c) developing and testing models suitable for describing the phase behavior of such mixtures, and (d) presenting the modeling results in generalized, practical formats suitable for use in process engineering calculations. During the present reporting period, our solubility apparatus was refurbished and restored to full service. To test the experimental apparatus and procedures used, measurements were obtained for the solubility Of C0{sub 2} in benzene at 160{degrees}F. Having confirmed the accuracy of the newly acquired data in comparison with our previous measurements and data reported in the literature for this test system, we have begun to measure the solubility of hydrogen in hexane. The measurements for this system will cover the temperature range from 160 to 280{degrees}F at pressures to 2,500 psia. As part of our model evaluation efforts, we examined the predictive abilities of an alternative approach we have proposed for calculating the phase behavior properties of highly non-ideal systems. Using this approach, the liquid phase fugacities generated from an equation of state (EOS) are augmented by a fugacity deviation function correction. The correlative abilities of this approach are compared with those of an EOS equipped with the recently introduced Wong-Sandler (MWS) mixing rules. These two approaches are compared with the current methods for vapor-liquid equilibrium (VLE) calculations, i.e., the EOS (0/0) approach with the van der Waals mixing rules and the split (y/0) approach. The evaluations were conducted on a database comprised of non-ideal low pressure binary systems as well as asymmetric high pressure binary systems. These systems are of interest in the coal liquefaction and utilization processes. The Peng-Robinson EOS was selected for the purposes of this evaluation.

Gasem, K.A.M.; Robinson, R.L., Jr.; Trvedi, N.J., Gao, W.

1997-09-01T23:59:59.000Z

424

Removal of copper and lead ions from aqueous solutions by adsorbent derived from sewage sludge  

Science Journals Connector (OSTI)

Adsorbent prepared from sewage sludge has been used for the adsorption of Cu2+ and Pb2+ from aqueous solutions. It was noted that an increase in removal efficiency achieved 72% and 56% when agitation time achieved 120 min, and a decrease in the removal efficiency from 81% and 70% to 36% and 40% when the heavy metals initial concentration from 10 mg L?1 to 80 mg L?1 for Cu2+ and Pb2+ concentration, the removal efficiency increased with the adsorbent concentration increased. The Langmuir model fitted the experimental data reasonably well. The adsorption capacities achieved 9.737 mg g?1 and 7.386 mg g?1 for the Cu2+ and Pb2+, respectively. Desorption studies were performed by using dilute hydrochloric acid. Quantitative recovery of the metal ion is possible. The mechanism of adsorption seems to be ion exchange.

YunBo Zhai; GuangMing Zeng; LaFang Wang; XianXun Wei; CaiTing Li; ShanHong Li

2011-01-01T23:59:59.000Z

425

Process removes Sr from nuclear wastes  

Science Journals Connector (OSTI)

Process removes Sr from nuclear wastes ... Scientists at Argonne National Laboratory have devised a chemical process for extracting and recovering strontium-90 from liquid nuclear wastes. ... Argonne chemist E. Philip Horwitz, head of the team, says it could be a significant aid in managing such radioactive wastes. ...

WARD WORTHY

1990-09-10T23:59:59.000Z

426

Removing dissolved inorganic contaminants from water  

SciTech Connect

This article describes the physicochemical treatment processes typically used to remove the more common inorganic contaminants from water and wastewater. These are precipitation, coprecipitation, adsorption, ion exchange, membrane separations by reverse osmosis and electrodialysis, and combinations of these processes. The general criteria for process selection are discussed, and the processes and their typical applications are described.

Clifford, D.; Subramonian, S.; Sorg, T.J.

1986-11-01T23:59:59.000Z

427

Method for Removing Precipitates in Biofuel  

At ORNL the application of ultrasonic energy, or sonication, has been shown to successfully remove or prevent the formation of 5090% of the precipitates in biofuels. Precipitates can plug filters as biodiesel is transported from one location to another, and often cannot be detected by visual inspection....

2010-12-08T23:59:59.000Z

428

Automatic Red Eye Removal for Digital Photography  

E-Print Network (OSTI)

Chapter 1 Automatic Red Eye Removal for Digital Photography FRANCESCA GASPARINI DISCo, Dipartimento The red eye effect is a well known problem in photography. It is often seen in amateur shots taken with a built-in flash, but the problem is also well known to professional photographers. Red eye is the red

Schettini, Raimondo

429

Plastic bottles > Remove lids (not recyclable)  

E-Print Network (OSTI)

Plastic bottles Please: > Remove lids (not recyclable) > Empty bottles > Rinse milk bottles, & other bottles if possible > Squash bottles www.st-andrews.ac.uk/estates/environment All types of plastic bottle accepted Clear, opaque and coloured bottles Labels can remain on X No plastic bags X No plastics

Brierley, Andrew

430

ASBESTOS PIPE-INSULATION REMOVAL ROBOT SYSTEM  

SciTech Connect

This final topical report details the development, experimentation and field-testing activities for a robotic asbestos pipe-insulation removal robot system developed for use within the DOE's weapon complex as part of their ER and WM program, as well as in industrial abatement. The engineering development, regulatory compliance, cost-benefit and field-trial experiences gathered through this program are summarized.

Unknown

2000-09-15T23:59:59.000Z

431

Removable partial overdentures for the irradiated patient  

SciTech Connect

Patients who have received radiotherapy to the head and neck area must avoid dental extractions and seek simplicity in treatment and home care follow-up. For partially edentulous patients, removable partial overdenture therapy can fulfill these goals while maintaining the high level of function and aesthetics desired by patients.11 references.

Rosenberg, S.W. (New York Univ. School of Dentistry, NY (USA))

1990-10-01T23:59:59.000Z

432

Pentek metal coating removal system: Baseline report  

SciTech Connect

The Pentek coating removal technology was tested and is being evaluated at Florida International University (FIU) as a baseline technology. In conjunction with FIU`s evaluation of efficiency and cost, this report covers evaluation conducted for safety and health issues. It is a commercially available technology and has been used for various projects at locations throughout the country. The Pentek coating removal system consisted of the ROTO-PEEN Scaler, CORNER-CUTTER{reg_sign}, and VAC-PAC{reg_sign}. They are designed to remove coatings from steel, concrete, brick, and wood. The Scaler uses 3M Roto Peen tungsten carbide cutters while the CORNER-CUTTER{reg_sign} uses solid needles for descaling activities. These hand tools are used with the VAC-PAC{reg_sign} vacuum system to capture dust and debris as removal of the coating takes place. The safety and health evaluation during the testing demonstration focused on two main areas of exposure: dust and noise. Dust exposure minimal, but noise exposure was significant. Further testing for each exposure is recommended because of the environment where the testing demonstration took place. It is feasible that the dust and noise levels will be higher in an enclosed operating environment of different construction. In addition, other areas of concern found were arm-hand vibration, whole-body, ergonomics, heat stress, tripping hazards, electrical hazards, machine guarding, and lockout/tagout.

NONE

1997-07-31T23:59:59.000Z

433

Method of preparation of removable syntactic foam  

DOE Patents (OSTI)

Easily removable, environmentally safe, low-density, syntactic foams are disclosed which are prepared by mixing insoluble microballoons with a solution of water and/or alcohol-soluble polymer to produce a pourable slurry, optionally vacuum filtering the slurry in varying degrees to remove unwanted solvent and solute polymer, and drying to remove residual solvent. The properties of the foams can be controlled by the concentration and physical properties of the polymer, and by the size and properties of the microballoons. The suggested solute polymers are non-toxic and soluble in environmentally safe solvents such as water or low-molecular weight alcohols. The syntactic foams produced by this process are particularly useful in those applications where ease of removability is beneficial, and could find use in packaging recoverable electronic components, in drilling and mining applications, in building trades, in art works, in the entertainment industry for special effects, in manufacturing as temporary fixtures, in agriculture as temporary supports and containers and for delivery of fertilizer, in medicine as casts and splints, as temporary thermal barriers, as temporary protective covers for fragile objects, as filters for particulate matter, which matter may be easily recovered upon exposure to a solvent, as in-situ valves (for one-time use) which go from maximum to minimum impedance when solvent flows through, and for the automatic opening or closing of spring-loaded, mechanical switches upon exposure to a solvent, among other applications.

Arnold, Jr., Charles (Albuquerque, NM); Derzon, Dora K. (Albuquerque, NM); Nelson, Jill S. (Albuquerque, NM); Rand, Peter B. (Albuquerque, NM)

1995-01-01T23:59:59.000Z

434

Long-term record of nss-sulfate and nitrate in aerosols on Midway Island, 19812000: Evidence of increased  

E-Print Network (OSTI)

aerosol along with greenhouse gases are better able to reproduce the surface temperature trends in the 20 of increased (now decreasing?) anthropogenic emissions from Asia Joseph M. Prospero and Dennis L. Savoie Center, New Mexico State University, Carlsbad, New Mexico, USA Received 19 November 2001; revised 14

Prospero, Joseph M.

435

Membrane systems for energy efficient separation of light gases  

SciTech Connect

Ethylene and propylene are two of the largest commodity chemicals in the United States and are major building blocks for the petrochemicals industry. These olefins are separated currently by cryogenic distillation which demands extremely low temperatures and high pressures. Over 75 billion pounds of ethylene and propylene are distilled annually in the US at an estimated energy requirement of 400 trillion BTU`s. Non-domestic olefin producers are rapidly constructing state-of-the-art plants. These energy-efficient plants are competing with an aging United States olefins industry in which 75% of the olefins producers are practicing technology that is over twenty years old. New separation opportunities are therefore needed to continually reduce energy consumption and remain competitive. Amoco has been a leader in incorporating new separation technology into its olefins facilities and has been aggressively pursuing non-cryogenic alternatives to light gas separations. The largest area for energy reduction is the cryogenic isolation of the product hydrocarbons from the reaction by-products, methane and hydrogen. This separation requires temperatures as low as {minus}150{degrees}F and pressures exceeding 450 psig. This CRADA will focus on developing a capillary condensation process to separate olefinic mixtures from light gas byproducts at temperatures that approach ambient conditions and at pressures less than 250 psig; this technology breakthrough will result in substantial energy savings. The key technical hurdle in the development of this novel separation concept is the precise control of the pore structure of membrane materials. These materials must contain specially-shaped channels in the 20-40A range to provide the driving force necessary to remove the condensed hydrocarbon products. In this project, Amoco is the technology end-user and provides the commercialization opportunity and engineering support.

Devlin, D.J.; Archuleta, T.; Barbero, R. [Los Alamos National Lab., NM (United States)] [and others

1997-04-01T23:59:59.000Z

436

Biomass and nutrient removal by willow clones in experimental bioenergy plantations in New York State  

Science Journals Connector (OSTI)

The development of short-rotation intensive cultural (SRIC) willow systems as a source of bioenergy and bioproducts is growing in the northeastern and midwestern United States. Important data for sustainable management such as nutrient removal and nutrient use efficiency in willow bioenergy plantations is lacking. This study reports wood biomass production, annual removal of nutrients, and nutrient use efficiency in experimental plantings of SRIC willow and poplar at Tully, New York. Effects of clone, fertilization, irrigation, planting density, and harvest cycle were analyzed. Annual biomass production of 1522 dryMg/ha removed 7586, 1011, 2732, 5279 and 45kg/ha/year of N, P, K, Ca and Mg, respectively. For all the variables studied, the responses depended on clone. Fertilization and irrigation increased rates of nutrient removal by means of increased biomass production. Unlike planting density, harvest cycle significantly affected rates of nutrient removal and nutrient use efficiency. For clone SV1 (Salix dasyclados), an irrigated and fertilized planting with a density of 36,960trees/ha harvested on a 3-year rotation had the highest biomass production and nutrient use efficiency, and the lowest rates of nutrient removal. The annual harvest cycle had the lowest nutrient use efficiency and the highest annual removal of nutrients suggesting that this choice would be most appropriate for biomass crops that are to be used as buffer strips to manage nutrient runoff from agricultural fields. An appropriate choice of clone, planting density, and harvest cycle could tailor the rates of nutrient removal and nutrient use efficiency to match the objective of the planting.

Hector G. Adegbidi; Timothy A. Volk; Edwin H. White; Lawrence P. Abrahamson; Russell D. Briggs; Donald H. Bickelhaupt

2001-01-01T23:59:59.000Z

437

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

DOE Patents (OSTI)

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

Aines, Roger D.; Bourcier, William L.

2014-08-19T23:59:59.000Z

438

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

DOE Patents (OSTI)

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

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

2010-11-09T23:59:59.000Z

439

Solubility Coefficients for Solar Liquids, a New Method to Quantify Undissolved Gases and Practical Recommendations  

Science Journals Connector (OSTI)

Abstract Solubility of nitrogen in propylene glycol/water mixtures (25%, 41.84% and 100% glycol by weight) have been determined in a temperature range from 10C to 110C using a static isochoric measuring method and are compared to the solubility of a typical solar liquid. To evaluate the amount of gas in a solar system it is necessary to measure the part of gases dissolved in the solar liquid, but also to consider the fraction of free gases (gas bubbles or gas cushions) in the system. Measuring this part was either not possible or only possible with a big technical effort until now. Therefore a new method was developed, which easily and fast identifies the volume of undissolved gases (Gas Bubble Test). The method was validated in extensive investigations in real solar systems.

Martin Heymann; Felix Panitz; Karin Rhling; Clemens Felsmann

2014-01-01T23:59:59.000Z

440

ASUWT JUDICIAL BOARD REMOVAL PROCESS "The ASUWT President shall establish and preside over the removal process, which shall commence  

E-Print Network (OSTI)

should not be removed. Additional time to submit supporting information may be requested and approvedASUWT JUDICIAL BOARD REMOVAL PROCESS "The ASUWT President shall establish and preside over the removal process, which shall commence within five (5) days after the Senate vote to bring removal

Borenstein, Elhanan

Note: This page contains sample records for the topic "gases removed increased" 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

GEI 41040G - Specification for Fuel Gases for COmbustion in Heavy-Duty Gas Turbines  

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

Gas Turbine Gas Turbine Revised, January 2002 GEI 41040G These instructions do not purport to cover all details or variations in equipment nor to provide for every possible contingency to be met in connection with installation, operation or maintenance. Should further information be desired or should particular problems arise which are not covered sufficiently for the purchaser's purposes the matter should be referred to the GE Company. © 1999 GENERAL ELECTRIC COMPANY Specification for Fuel Gases for Combustion in Heavy-Duty Gas Turbines GEI 41040G Specification for Fuel Gases for Combustion in Heavy-Duty Gas Turbines 2 TABLE OF CONTENTS I. INTRODUCTION 4 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

442

Dissipative Dynamics of a Josephson Junction In the Bose-Gases  

E-Print Network (OSTI)

The dissipative dynamics of a Josephson junction in the Bose-gases is considered within the framework of the model of a tunneling Hamiltonian. The effective action which describes the dynamics of the phase difference across the junction is derived using functional integration method. The dynamic equation obtained for the phase difference across the junction is analyzed for the finite temperatures in the low frequency limit involving the radiation terms. The asymmetric case of the Bose-gases with the different order parameters is calculated as well.

R. A. Barankov; S. N. Burmistrov

2003-01-09T23:59:59.000Z

443

Spin noise spectroscopy to probe quantum states of ultracold fermionic atom gases  

SciTech Connect

We theoretically demonstrate that optical measurements of electron spin noise can be a spectroscopic probe of the entangled quantum states of ultracold fermionic atom gases and unambiguously reveal the detailed nature of the underlying interatomic correlations. Different models of the effective interatomic interactions predict entirely new sets of resonances in the spin noise spectrum. Once the correct effective interatomic interaction model is identified, the detailed noise line shapes of the spin noise can be used to constrain this model. We estimate the magnitude of spin noise signals expected in ultracold fermionic atom gases via noise measurements in classical alkali vapors, which demonstrate the feasibility of this approach.

Mihaila, Bogdan; Blagoev, Krastan B.; Smith, Darryl L. [Theoretical Division, Los Alamos National Laboratory, Los Alamos, New Mexico 87545 (United States); Crooker, Scott A.; Rickel, Dwight G. [National High Magnetic Field Laboratory, Los Alamos National Laboratory, Los Alamos, New Mexico 87545 (United States); Littlewood, Peter B. [Cavendish Laboratory, Madingley Road, Cambridge CB3 0HE (United Kingdom)

2006-12-15T23:59:59.000Z

444

Removal of polycyclic aromatic hydrocarbons from surfactant solutions by selective sorption with organo-bentonite  

Science Journals Connector (OSTI)

Abstract Surfactant-enhanced soil washing is known to be an effective remediation approach for contaminated soils and groundwater. However, the recovery of surfactant solutions after soil washing is required for reducing the operation costs of the soil washing process. In this study, selective sorption with organo-bentonite was employed for the removal of polycyclic aromatic hydrocarbons (PAHs) from aqueous surfactant solution as a potential means of recovering surfactant solution after soil washing. The sorption of phenanthrene onto organo-bentonite from surfactant solution was well described by the pseudo-second-order kinetic model and the linear sorption isotherm model, respectively. \\{PAHs\\} can be effectively removed by organo-bentonite from surfactant solutions in a high proportion relative to the sorption loss of surfactant under all experimental conditions. The selectivity for PAH removal to surfactant sorption increased with increasing PAH hydrophobicity and surfactant hydrophilicity, but decreased with increasing surfactant concentration. However, increasing the organo-bentonite dose did not have obvious effect on the selectivity for surfactant recovery since it synchronously enhanced phenanthrene removal and surfactant sorption. The sorbent of organo-bentonite could be repeatedly used for recovering surfactant solution, which greatly reduced the sorption loss of surfactant and subsequently increased the selectivity for surfactant recovery considerably. The results suggest that selective sorption with organo-bentonite provides an alternative means of recovering surfactant solution after soil washing.

Wenjun Zhou; Xuehao Wang; Cuiping Chen; Lizhong Zhu

2013-01-01T23:59:59.000Z

445

Improved Processes to Remove Naphthenic Acids  

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

Improved Processes to Remove Naphthenic Acids Improved Processes to Remove Naphthenic Acids Final Technical Report (From October 1, 2002 to September 30, 2005) Principle Authors Aihua Zhang, Qisheng Ma, Kangshi Wang, Yongchun Tang (co-PI), William A. Goddard (PI), Date Report was issued: December 9, 2005 DOE Award number: DE-FC26-02NT15383 Name and Address of Submitting Organization California Institute of Technology 1200 East California Blvd., Pasadena, CA91125 Disclaimer This report was prepared as an account of work sponsored by an agency of the United States Government. Neither the United States Government nor any agency thereof, nor any of their employees, makes any warranty, express or implied, or assumes any legal liability or responsibility for the accuracy, completeness, or usefulness of any

446

TMI defueling project fuel debris removal system  

SciTech Connect

The three mile Island Unit 2 (TMI-2) pressurized water reactor loss-of-coolant accident on March 28, 1979, presented the nuclear community with many challenging remediation problems; most importantly, the removal of the fission products within the reactor containment vessel. To meet this removal problem, an air-lift system (ALS) can be used to employ compressed air to produce the motive force for transporting debris. Debris is separated from the transport stream by gravity separation. The entire method does not rely on any moving parts. Full-scale testing of the ALS at the Idaho National Engineering Laboratory (INEL) has demonstrated the capability of transporting fuel debris from beneath the LCSA into a standard fuel debris bucket at a minimum rate of 230 kg/min.

Burdge, B.

1992-01-01T23:59:59.000Z

447

TMI defueling project fuel debris removal system  

SciTech Connect

The three mile Island Unit 2 (TMI-2) pressurized water reactor loss-of-coolant accident on March 28, 1979, presented the nuclear community with many challenging remediation problems; most importantly, the removal of the fission products within the reactor containment vessel. To meet this removal problem, an air-lift system (ALS) can be used to employ compressed air to produce the motive force for transporting debris. Debris is separated from the transport stream by gravity separation. The entire method does not rely on any moving parts. Full-scale testing of the ALS at the Idaho National Engineering Laboratory (INEL) has demonstrated the capability of transporting fuel debris from beneath the LCSA into a standard fuel debris bucket at a minimum rate of 230 kg/min.

Burdge, B.

1992-08-01T23:59:59.000Z

448

Removal of arsenic compounds from petroliferous liquids  

DOE Patents (OSTI)

Described is a process for removing arsenic from petroliferous derived liquids by contacting said liquid at an elevated temperature with a divinylbenzene-crosslinked polystyrene having catechol ligands anchored thereon. Also, described is a process for regenerating spent catecholated polystyrene by removal of the arsenic bound to it from contacting petroliferous liquid as described above and involves: a. treating said spent catecholated polystyrene, at a temperature in the range of about 20.degree. to 100.degree. C. with an aqueous solution of at least one carbonate and/or bicarbonate of ammonium, alkali and alkaline earth metals, said solution having a pH between about 8 and 10 and, b. separating the solids and liquids from each other. Preferably the regeneration treatment is in two steps wherein step (a) is carried out with an aqueous alcoholic carbonate solution containing lower alkyl alcohol, and, steps (a) and (b) are repeated using a bicarbonate.

Fish, Richard H. (Berkeley, CA)

1985-01-01T23:59:59.000Z

449

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

450

Categorical Exclusion 4568, Crane Removal Project  

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

l)eterminationFornl l)eterminationFornl Project Title: Crane Removal Project (4568) Program or Program Office: Y -12 Site Office Location: Oak Ridge Tennessee Project Description: This work scope is to remove an old legacy crane trolley and old crane operated cab. General Administration/Management DA I - Routine business actions DA2 - Administrative contract amendments DA4 - Interpretations/rulings for existing regulations DA5 - Regulatory interpretations without environmental effect DA6 - Procedural rulemakings upgrade DA7 - Transfer of property, use unchanged DA8 - Award of technical support/M&O/personal service contracts DA9 - Info gathering, analysis, documentation, dissemination, and training DAIO - Reports on non-DOE legislation DA II - Technical advice and planning assistance

451

Process for removing mercury from aqueous solutions  

DOE Patents (OSTI)

A process for removing mercury from water to a level not greater than two parts per billion wherein an anion exchange material that is insoluble in water is contacted first with a sulfide containing compound and second with a compound containing a bivalent metal ion forming an insoluble metal sulfide. To this treated exchange material is contacted water containing mercury. The water containing not more than two parts per billion of mercury is separated from the exchange material.

Googin, John M. (Oak Ridge, TN); Napier, John M. (Oak Ridge, TN); Makarewicz, Mark A. (Knoxville, TN); Meredith, Paul F. (Knoxville, TN)

1986-01-01T23:59:59.000Z

452

REMOVAL OF LEGACY PLUTONIUM MATERIALS FROM SWEDEN  

SciTech Connect

U.S. Department of Energys National Nuclear Security Administration (NNSA) Office of Global Threat Reduction (GTRI) recently removed legacy plutonium materials from Sweden in collaboration with AB SVAFO, Sweden. This paper details the activities undertaken through the U.S. receiving site (Savannah River Site (SRS)) to support the characterization, stabilization, packaging and removal of legacy plutonium materials from Sweden in 2012. This effort was undertaken as part of GTRIs Gap Materials Program and culminated with the successful removal of plutonium from Sweden as announced at the 2012 Nuclear Security Summit. The removal and shipment of plutonium materials to the United States was the first of its kind under NNSAs Global Threat Reduction Initiative. The Environmental Assessment for the U.S. receipt of gap plutonium material was approved in May 2010. Since then, the multi-year process yielded many first time accomplishments associated with plutonium packaging and transport activities including the application of the of DOE-STD-3013 stabilization requirements to treat plutonium materials outside the U.S., the development of an acceptance criteria for receipt of plutonium from a foreign country, the development and application of a versatile process flow sheet for the packaging of legacy plutonium materials, the identification of a plutonium container configuration, the first international certificate validation of the 9975 shipping package and the first intercontinental shipment using the 9975 shipping package. This paper will detail the technical considerations in developing the packaging process flow sheet, defining the key elements of the flow sheet and its implementation, determining the criteria used in the selection of the transport package, developing the technical basis for the package certificate amendment and the reviews with multiple licensing authorities and most importantly integrating the technical activities with the Swedish partners.

Dunn, Kerry A. [Savannah River National Laboratory; Bellamy, J. Steve [Savannah River National Laboratory; Chandler, Greg T. [Savannah River National Laboratory; Iyer, Natraj C. [U.S. Department of Energy, National Nuclear Security Administration, Office of; Koenig, Rich E.; Leduc, D. [Savannah River National Laboratory; Hackney, B. [Savannah River National Laboratory; Leduc, Dan R. [Savannah River National Laboratory

2013-08-18T23:59:59.000Z

453

Removal of copper from ferrous scrap  

DOE Patents (OSTI)

A process for removing copper from ferrous or other metal scrap in which the scrap is contacted with a polyvalent metal sulfide slag in the presence of an excess of copper-sulfide forming additive to convert the copper to copper sulfide which is extracted into the slag to provide a ratio of copper in the slag to copper in the metal scrap of at least about 10.

Blander, M.; Sinha, S.N.

1987-07-30T23:59:59.000Z

454

Process for removing mercury from aqueous solutions  

DOE Patents (OSTI)

A process for removing mercury from water to a level not greater than two parts per billion wherein an anion exchange material that is insoluble in water is contacted first with a sulfide containing compound and second with a compound containing a bivalent metal ion forming an insoluble metal sulfide. To this treated exchange material is contacted water containing mercury. The water containing not more than two parts per billion of mercury is separated from the exchange material.

Googin, J.M.; Napier, J.M.; Makarewicz, M.A.; Meredith, P.F.

1985-03-04T23:59:59.000Z

455

Removal of copper from ferrous scrap  

DOE Patents (OSTI)

A process for removing copper from ferrous or other metal scrap in which the scrap is contacted with a polyvalent metal sulfide slag in the presence of an excess of copper-sulfide forming additive to convert the copper to copper sulfide which is extracted into the slag to provide a ratio of copper in the slag to copper in the metal scrap of at least about 10.

Blander, Milton (12833 S. 82nd Ct., Palos Park, IL 60464); Sinha, Shome N. (5748 Drexel, 2A, Chicago, IL 60637)

1990-01-01T23:59:59.000Z

456

Assessment of the impact on crops of effluent gases from geothermal energy development in the Imperial Valley, California  

SciTech Connect

We have assessed the potential impact of regionally dispersed sources of geothermal gaseous effluents on crops in the Imperial Valley. We used a detailed model of the photosynthesis and growth of sugar beets fumigated by H/sub 2/S and CO/sub 2/ and generalized from the model calculations to other crops. Model calculations were made with estimates of time series of expected ground-level concentrations of H/sub 2/S and CO/sub 2/ calculated by the Air Quality Assessment element of the Imperial Valley Environmental Project (IVEP) at 22 locations around the valley. Results indicate that in the absence of interactions with other ambient pollutant gases, all locations would experience an increase (from slight to significant) in total growth of sugar beets. Seven locations will experience an increase of at least 10%. We calculated the emissions rate at which negative effects cancel out the benefits of H/sub 2/S fertilization; in the worst case, emission rates are expected to be no more than 1/13 this crossover rate. The expected emission rate will be less than that necessary for negative effects on the most sensitive species (such as alfalfa) by a factor of 4. Similar results for other crops are summarized in the report. If CO/sub 2/ emissions are increased proportionately, the dominance of deleterious effects is not expected to occur even under maximum development as set forth in IVEP scenario projections. 23 references, 8 figures, 6 tables.

Kercher, J.R.

1981-05-22T23:59:59.000Z

457

Detection of Irradiated Frozen Deboned Seafood with the Level of Radiolytic H2 and CO Gases as a Probe  

Science Journals Connector (OSTI)

A method to detect irradiated frozen shrimp without cuticle, cod slices, and deshelled oyster has been developed based on the fact that radiolytic H2 and CO gases are retained in the irradiated samples for a certain period during the storage. These gases ...

Masakazu Furuta; Takaaki Dohmaru; Tadashi Katayama; Hirokazu Toratani; Atsuhiko Takeda

1997-10-15T23:59:59.000Z

458

Method and apparatus for separating gases based on electrically and magnetically enhanced monolithic carbon fiber composite sorbents  

DOE Patents (OSTI)

A method for separating gases or other fluids involves placing a magnetic field on a monolithic carbon fiber composite sorption material to more preferentially attract certain gases or other fluids to the sorption material to which a magnetic field is applied. This technique may be combined with the known pressure swing adsorption'' technique utilizing the same sorption material. 1 fig.

Judkins, R.R.; Burchell, T.D.

1999-07-20T23:59:59.000Z

459

Method and apparatus for separating gases based on electrically and magnetically enhanced monolithic carbon fiber composite sorbents  

DOE Patents (OSTI)

A method for separating gases or other fluids involves placing a magnetic field on a monolithic carbon fiber composite sorption material to more preferentially attract certain gases or other fluids to the sorption material to which a magnetic field is applied. This technique may be combined with the known "pressure swing adsorption" technique utilizing the same sorption material.

Judkins, Roddie R. (9917 Rainbow Dr., Knoxville, TN 37922); Burchell, Timothy D. (109 Greywood Pl., Oak Ridge, TN 37830)

1999-01-01T23:59:59.000Z

460

Photoconductivity and luminescence in GaSe crystals at high levels of optical excitation  

SciTech Connect

The photoconductivity and luminescence of GaSe layered crystals at high levels of optical excitation are studied experimentally. The specific features observed in the photoconductivity and photoluminescence spectra are controlled by the nonlinear optical absorption in the region of excitonic resonance.

Kyazym-zade, A. G.; Salmanov, V. M., E-mail: vagif_salmanov@yahoo.com; Salmanova, A. A. [Baku State University (Azerbaijan); Alieva, A. M.; Ibaeva, R. Z. [National Academy of Sciences, Institute of Physics (Azerbaijan)

2010-03-15T23:59:59.000Z

Note: This page contains sample records for the topic "gases removed increased" 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

Effects of Biochar and Basalt Additions on Carbon Sequestration and Fluxes of Greenhouse Gases in Soils  

E-Print Network (OSTI)

Effects of Biochar and Basalt Additions on Carbon Sequestration and Fluxes of Greenhouse Gases Emissions--Carbon Dioxide Emissions--Sequestration and Storage--Biochar--Basalt--Organic Fertilizers, this investigation focuses on the range of potential of different soil additives to enhance sequestration and storage

Vallino, Joseph J.

462

Operational aspects of the desulfurization process of energy gases mimics in biotrickling filters5  

E-Print Network (OSTI)

. Introduction Energy rich off-gases such as biogas are sometimes not used for electric power generation due impurities. H2S concentrations in biogas can range from 0.1 to 5 We dedicate this article to the memory/v (1000e20,000 ppmv), whereas the specifications for the maximum content of H2S in typical biogas

463

Bose-Einstein Condensation in Atomic Gases Jerzy Zachorowski and Wojciech Gawlik  

E-Print Network (OSTI)

. It is instructive to compare orders of magnitude typical for the thermal and condensed gas samples. For atom gasBose-Einstein Condensation in Atomic Gases Jerzy Zachorowski and Wojciech Gawlik M. Smoluchowski on the Bose-Einstein condensate. We also present main parameters and expected characteristics of the first Pol

464

UA Researchers design a catalyst that neutralizes the gases responsible for climate change  

E-Print Network (OSTI)

UA Researchers design a catalyst that neutralizes the gases responsible for climate change Toxic Researchers at the University of Alicante have developed and patented a novel catalyst capable of decomposing gas streams. "However, nitrous oxide can be decomposed at lower temperatures using a suitable catalyst

Escolano, Francisco

465

Radiative-convective model of warming Mars with artificial greenhouse gases  

E-Print Network (OSTI)

spectra of seven artificial greenhouse gases (CF4, C2F6, C3F8, SF6, CF3Cl, CF3Br, CF2Cl2 ecosynthesis, CF4, C2F6, and SF6 were 17%, 49%, and 48% as effective as C3F8, respectively. The optimal mixture

Kite, Edwin

466

A Biomass-based Model to Estimate the Plausibility of Exoplanet Biosignature Gases  

E-Print Network (OSTI)

Biosignature gas detection is one of the ultimate future goals for exoplanet atmosphere studies. We have created a framework for linking biosignature gas detectability to biomass estimates, including atmospheric photochemistry and biological thermodynamics. The new framework is intended to liberate predictive atmosphere models from requiring fixed, Earth-like biosignature gas source fluxes. New biosignature gases can be considered with a check that the biomass estimate is physically plausible. We have validated the models on terrestrial production of NO, H2S, CH4, CH3Cl, and DMS. We have applied the models to propose NH3 as a biosignature gas on a "cold Haber World," a planet with a N2-H2 atmosphere, and to demonstrate why gases such as CH3Cl must have too large of a biomass to be a plausible biosignature gas on planets with Earth or early-Earth-like atmospheres orbiting a Sun-like star. To construct the biomass models, we developed a functional classification of biosignature gases, and found that gases (such...

Seager, S; Hu, R

2013-01-01T23:59:59.000Z

467

Article published Greenhouse Gases: Science and Technology DOI: 10.1002/ghg.1395  

E-Print Network (OSTI)

Article published Greenhouse Gases: Science and Technology DOI: 10.1002/ghg.1395 National Corridors.1002/ghg.1395 #12;1 Introduction The need to reduce greenhouse gas (GHG) emissions by present energy.1, 2 Carbon dioxide (CO2) is the most worrisome GHG because of its long residence time

Paris-Sud XI, Université de

468

Ballistic spin transport in exciton gases A. V. Kavokin,1, 2  

E-Print Network (OSTI)

, or spin-optronics challeng- ing. How possibly one can explore the current, which is carried by neutral are possible in exciton and exciton-polariton Bose gases. Bosonic spintronics or spin-optronics operates,28 . Combined with evident advantages of bosonic amplifica- tion and low dephasing, this makes spin-optronics

Paris-Sud XI, Université de

469

Gas Chromatographic Measurement of Trace Oxygen and Other Dissolved Gases in Thermally Stressed Jet Fuel  

Science Journals Connector (OSTI)

......additional light hydrocarbon gases (e.g...stream, and the data can be obtained...system. The output data from this analytical...F33615-87-C-2714 and the Combustion and Heat Transfer Studies...from deoxygenated hydrocarbons: I. General features......

Wayne A. Rubey; Richard C. Striebich; Michael D. Tissandier; Debra A. Tirey; Steven D. Anderson

1995-08-01T23:59:59.000Z

470

Experimental observation of a traveling plasma grating formed by two crossing filaments in gases  

SciTech Connect

The spatial motion and effective duration of a traveling plasma grating formed by two interfering femtosecond laser filaments in gases is characterized by its Doppler effect imparted on a probe pulse. The shift velocity determined experimentally agrees with the theoretical calculations.

Durand, Magali [Laboratoire d'Optique Appliquee, ENSTA ParisTech-Ecole Polytechnique-CNRS, 91761 Palaiseau (France); ONERA, Chemin de la Huniere, 91761 Palaiseau (France); Liu Yi; Forestier, Benjamin; Houard, Aurelien; Mysyrowicz, Andre [Laboratoire d'Optique Appliquee, ENSTA ParisTech-Ecole Polytechnique-CNRS, 91761 Palaiseau (France)

2011-03-21T23:59:59.000Z

471

Anode supported single chamber solid oxide fuel cells operating in exhaust gases of thermal engine  

E-Print Network (OSTI)

Anode supported single chamber solid oxide fuel cells operating in exhaust gases of thermal engine fuel cells are usually described as devices able to convert chemical energy into electrical energy. Conventional solid oxide fuel cells are separated into two compartments containing each electrode split

Boyer, Edmond

472

Abstract--Energy consumption and the concomitant Green House Gases (GHG) emissions of network infrastructures are  

E-Print Network (OSTI)

Abstract--Energy consumption and the concomitant Green House Gases (GHG) emissions of network on the overall power consumption and on the GHG emissions with just 25% of green energy sources. I. INTRODUCTION]. In the zero carbon approach, renewable (green) energy sources (e.g. sun, wind, tide) are employed and no GHGs

Politècnica de Catalunya, Universitat

473

Kolmogorov-Sinai entropy for dilute gases in equilibrium H. van Beijeren,1  

E-Print Network (OSTI)

. Posch,3 and Ch. Dellago3,4 1 Institute for Theoretical Physics, University of Utrecht, Postbus 80006, 3508 TA Utrecht, The Netherlands 2 Institute for Physical Science and Technology and Department the kinetic theory of gases have been applied to compute the chaotic properties of simple systems such as hard

Dellago, Christoph

474

Towards a history of the international industrial gases industry Ray Stokes, Ralf Banken, and Matthias Phl  

E-Print Network (OSTI)

industrial revolution" and their component companies. From David Landes's classic study, The Unbound of the industries of the second industrial revolution has been virtually ignored in this scholarship to date1 Towards a history of the international industrial gases industry Ray Stokes, Ralf Banken

Guo, Zaoyang

475

Changes in mercury bioaccumulation in an apex predator in response to removal of an introduced competitor  

E-Print Network (OSTI)

Changes in mercury bioaccumulation in an apex predator in response to removal of an introduced and decreased mercury concentrations in remaining fish. Instead, we observed a significant increase in lake web structure can influence MeHg concentrations in top predators. Keywords Mercury Á Food web Á Fish

Kraft, Clifford E.

476

RCS pressure under reduced inventory conditions following a loss of residual heat removal  

SciTech Connect

The thermal-hydraulic response of a closed-reactor coolant system to loss of residual heat removal (RHR) cooling is investigated. The processes examined include: core coolant boiling and steam generator reflux condensation, pressure increase on the primary side, heat transfer mechanisms on the steam generator primary and secondary sides, and effects of noncondensible gas on heat transfer processes.

Palmrose, D.E.; Hughes, E.D.; Johnsen, G.W.

1992-08-01T23:59:59.000Z

477

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

478

SULFURIC ACID REMOVAL PROCESS EVALUATION: LONG-TERM RESULTS  

SciTech Connect

The objective of this project is to demonstrate the use of alkaline reagents injected into the furnace of coal-fired boilers as a means of controlling sulfuric acid emissions. The project is being co-funded by the U.S. DOE National Energy Technology Laboratory, under Cooperative Agreement DE-FC26-99FT40718, along with EPRI, the American Electric Power Company (AEP), FirstEnergy Corp., the Tennessee Valley Authority, and Dravo Lime, Inc. Sulfuric acid controls are becoming of increasing interest to power generators with coal-fired units for a number of reasons. Sulfuric acid is a Toxic Release Inventory species and can cause a variety of plant operation problems such as air heater plugging and fouling, back-end corrosion, and plume opacity. These issues will likely be exacerbated with the retrofit of selective catalytic reduction (SCR) for NO{sub x} control on many coal-fired plants, as SCR catalysts are known to further oxidize a portion of the flue gas SO{sub 2} to SO{sub 3}. The project previously tested the effectiveness of furnace injection of four different calcium-and/or magnesium-based alkaline sorbents on full-scale utility boilers. These reagents were tested during four one- to two-week tests conducted on two FirstEnergy Bruce Mansfield Plant (BMP) units. One of the sorbents tested was a magnesium hydroxide byproduct slurry produced from a modified Thiosorbic{reg_sign} Lime wet flue gas desulfurization system. The other three sorbents are available commercially and include dolomite, pressure-hydrated dolomitic lime, and commercial magnesium hydroxide. The dolomite reagent was injected as a dry powder through out-of-service burners, while the other three reagents were injected as slurries through air-atomizing nozzles inserted through the front wall of the upper furnace, either across from the nose of the furnace or across from the pendant superheater tubes. After completing the four one- to two-week tests, the most promising sorbents were selected for longer-term (approximately 25-day) full-scale tests on two different units. The longer-term tests were conducted to confirm the effectiveness of the sorbents tested over extended operation on two different boilers, and to determine balance-of-plant impacts. The first long-term test was conducted on FirstEnergy's BMP, Unit 3, and the second test was conducted on AEP's Gavin Plant, Unit 1. The Gavin Plant testing provided an opportunity to evaluate the effects of sorbent injected into the furnace on SO{sub 3} formed across an operating SCR reactor. This report presents the results from those long-term tests. The tests determined the effectiveness of injecting commercially available magnesium hydroxide slurry (Gavin Plant) and byproduct magnesium hydroxide slurry (both Gavin Plant and BMP) for sulfuric acid control. The results show that injecting either slurry could achieve up to 70 to 75% overall sulfuric acid removal. At BMP, this overall removal was limited by the need to maintain acceptable electrostatic precipitator (ESP) particulate control performance. At Gavin Plant, the overall sulfuric acid removal was limited because the furnace injected sorbent was less effective at removing SO{sub 3} formed across the SCR system installed on the unit for NOX control than at removing SO{sub 3} formed in the furnace. The long-term tests also determined balance-of-plant impacts from slurry injection during the two tests. These include impacts on boiler back-end temperatures and pressure drops, SCR catalyst properties, ESP performance, removal of other flue gas species, and flue gas opacity. For the most part the balance-of-plant impacts were neutral to positive, although adverse effects on ESP performance became an issue during the BMP test.

Gary M. Blythe; Richard McMillan

2002-07-03T23:59:59.000Z

479

United Kingdom HEU Removal | National Nuclear Security Administration  

National Nuclear Security Administration (NNSA)

HEU Removal United Kingdom HEU Removal Location United Kingdom United States 52 24' 15.1416" N, 1 34' 55.3116" W See map: Google Maps Javascript is required to view this map...

480

Hanford Begins New Campaign to Remove Excess Water from Double...  

Energy Savers (EERE)

Hanford Begins New Campaign to Remove Excess Water from Double-Shell Tanks Hanford Begins New Campaign to Remove Excess Water from Double-Shell Tanks September 30, 2014 - 12:00pm...

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


481

Removing nuclear waste, one shipment at a time  

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

Removing nuclear waste, one shipment at a time Removing nuclear waste, one shipment at a time The Lab's 1,000th shipment of transuranic waste recently left Los Alamos, on its way...

482

Process for removing technetium from iron and other metals  

DOE Patents (OSTI)

A process for removing technetium from iron and other metals comprises the steps of converting the molten, alloyed technetium to a sulfide dissolved in manganese sulfide, and removing the sulfide from the molten metal as a slag. 4 figs.

Leitnaker, J.M.; Trowbridge, L.D.

1999-03-23T23:59:59.000Z

483

EM's SPRU Celebrates Waste Removal Success, Safety Milestone...  

Office of Environmental Management (EM)

EM's SPRU Celebrates Waste Removal Success, Safety Milestone EM's SPRU Celebrates Waste Removal Success, Safety Milestone February 27, 2014 - 12:00pm Addthis Members of the EM and...

484

Nitrogen Removal From Low Quality Natural Gas  

SciTech Connect

Natural gas provides more than one-fifth of all the primary energy used in the United States. It is especially important in the residential sector, where it supplies nearly half of all the energy consumed in U.S. homes. However, significant quantities of natural gas cannot be produced economically because its quality is too low to enter the pipeline transportation system without some type of processing, other than dehydration, to remove the undesired gas fraction. Such low-quality natural gas (LQNG) contains significant concentration or quantities of gas other than methane. These non- hydrocarbons are predominantly nitrogen, carbon dioxide, and hydrogen sulfide, but may also include other gaseous components. The nitrogen concentrations usually exceeds 4%. Nitrogen rejection is presently an expensive operation which can present uneconomic scenarios in the potential development of natural gas fields containing high nitrogen concentrations. The most reliable and widely used process for nitrogen rejection from natural gas consists of liquefying the feed stream using temperatures in the order of - 300{degrees}F and separating the nitrogen via fractionation. In order to reduce the gas temperature to this level, the gas is compressed, cooled by mullet-stream heat exchangers, and expanded to low pressure. Significant energy for compression and expensive materials of construction are required. Water and carbon dioxide concentrations must be reduced to levels required to prevent freezing. SRI`s proposed research involves screening new nitrogen selective absorbents and developing a more cost effective nitrogen removal process from natural gas using those compounds. The long-term objective of this project is to determine the technical and economical feasibility of a N{sub 2}2 removal concept based on complexation of molecular N{sub 2} with novel complexing agents. Successful development of a selective, reversible, and stable reagent with an appropriate combination of capacity and N{sub 2} absorption/desorption characteristics will allow selective separation of N{sub 2} from LQNG.

Alvarado, D.B.; Asaro, M.F.; Bomben, J.L.; Damle, A.S.; Bhown, A.S.

1997-10-01T23:59:59.000Z

485

Reactive gases evolved during pyrolysis of Devonian oil shale  

SciTech Connect

Computer modeling of oil shale pyrolysis is an important part of the Lawrence Livermore National Laboratory (LLNL) Oil Shale Program. Models containing detailed chemistry have been derived from an investigation of Colorado oil shale. We are currently attempting to use models to treat more completely reactions of nitrogen and sulfur compounds in the retort to better understand emissions. Batch retorting work on Devonian oil shale is proving particularly useful for this study of nitrogen/sulfur chemistry. Improved analytical methods have been developed to quantitatively determine reactive volatiles at the parts-per-million level. For example, the triple quadrupole mass spectrometer (TQMS) is used in the chemical ionization (CI) mode to provide real-time analytical data on ammonia evolution as the shale is pyrolyzed. A heated transfer line and inlet ensure rapid and complete introduction of ammonia to the instrument by preventing water condensation. Ammonia and water release data suitable for calculating kinetic parameters have been obtained from a New Albany Shale sample. An MS/MS technique with the TQMS in the electron ionization (EI) mode allows hydrogen sulfide, carbonyl sulfide, and certain trace organic sulfur compounds to be monitored during oil shale pyrolysis. Sensitivity and selectivity for these compounds have been increased by applying artificial intelligence techniques to tuning of the spectrometer. Gas evolution profiles (100 to 900/sup 0/C) are reported for hydrogen sulfide, water, ammonia, and trace sulfur species formed during pyrolysis of Devonian oil shale. Implications for retorting chemistry are discussed. 18 refs., 11 figs., 3 tabs.

Coburn, T.T.; Crawford, R.W.; Gregg, H.R.; Oh, M.S.

1986-11-01T23:59:59.000Z

486

Estimating Hydro's Contribution to the control of Greenhouse Gases  

SciTech Connect

One of the environmental effects of hydropower operation that should be evaluated in licensing decisions is the general benefit to air quality. Hydropower's contribution to the reduction of greenhouse gas (GHG) emissions is an increasingly important component of these air quality benefits. The Oak Ridge Competitive Electricity Dispatch (ORCED) computer model is one method that can be used to quantify these benefits. ORCED provides a relatively simple method that is applicable and cost-effective and that has been successfully applied in other GHG studies. ORCED can be used to calculate a region-specific value of the carbon intensity factor (CIF, kg carbon/MWh) that would be associated with likely replacement power (i.e., a regionally representative mix of coal, gas, and other energy sources). The project's plant factor and operational mode (e.g, baseload versus peaking) can also be incorporated in the CIF calculation. The resulting parameter can then be multiplied by the energy output of the hydropower project that is being analyzed to estimate a CO{sub 2} emission value that is avoided by the project's operation.

Sale, Michael J [ORNL; Hadley, Stanton W [ORNL

2002-01-01T23:59:59.000Z

487

Compensatory Feeding Following a Predator Removal Program : Detection and Mechanisms, 1982-1996 Progress Report.  

SciTech Connect

Predator removal is one of the oldest management tools in existence, with evidence that ancient Greeks used a bounty reward for wolves over 3,000 years ago (Anonymous 1964). Efforts to control predators on fish have been documented in scientific journals for at least 60 years (Eschmeyer 1937; Lagler 1939; Foerster and Ricker 1941; Smith and Swingle 1941; Jeppson and Platts 1959), and has likely been attempted for much longer. Complete eradication of a target species from a body of water has rarely been the objective of predator removal programs, which instead have attempted to eliminate predators from specific areas, to reduce the density or standing stock of predators, or to kill the largest individuals in the population (Meronek et al. 1996). In evaluating management programs that remove only part of a predator population, the compensatory response(s) of the remaining predators must be considered. Some potential compensatory responses by remaining individuals include increased reproductive output, increased growth rate, or increased consumption of certain prey species (Jude et al. 1987). If compensation by predators that remain in the system following a removal effort occurs, it may reduce the effectiveness of the predator control program. Northern pike-minnow Ptychocheilus oregonensis (formerly called northern squawfish) consume juvenile salmon in rivers, lakes, and reservoirs in British Columbia, Washington, Idaho, Oregon, and California. Northern pikeminnow have been estimated to consume about 11% of all juvenile salmon that migrate through John Day Reservoir on the Columbia River (Rieman et al. 1991). Modeling studies suggested that removal of 20% of the northern pikeminnow population in John Day Reservoir would result in a 50% decrease in predation-related mortality of juvenile salmon migrating through this reach (Beamesderfer et al. 1991). Since the early 1940's, other programs have been implemented to remove northern pikeminnow, with hopes of improving the survival of juvenile salmon (Ricker 1941; Jeppson and Platts 1959).

Petersen, James H.

2002-02-28T23:59:59.000Z

488

Electrostatic cleaning system for removal of sand from solar panels  

Science Journals Connector (OSTI)

Abstract An improved cleaning system has been developed that uses electrostatic force to remove sand from the surface of solar panels. A single-phase high voltage is applied to parallel wire electrodes embedded in the cover glass plate of a solar panel. It has been demonstrated that more than 90% of the adhering sand is repelled from the surface of the slightly inclined panel after the cleaning operation. The performance of the system was further improved by improving the electrode configuration and introducing natural wind on the surface of the panel, even when the deposition of sand on the panel is extremely high. The power consumption of this system is virtually zero. This technology is expected to increase the effective efficiency of mega solar power plants constructed in deserts at low latitudes.

Hiroyuki Kawamoto; Takuya Shibata

2015-01-01T23:59:59.000Z

489

Development of efficiency-enhanced cogeneration system utilizing high-temperature exhaust-gas from a regenerative thermal oxidizer for waste volatile-organic-compound gases  

Science Journals Connector (OSTI)

We have developed a gas-turbine cogeneration system that makes effective use of the calorific value of the volatile organic compound (VOC) gases exhausted during production processes at a manufacturing plant. The system utilizes the high-temperature exhaust-gas from the regenerative thermal oxidizer (RTO) which is used for incinerating VOC gases. The high-temperature exhaust gas is employed to resuperheat the steam injected into the gasturbine. The steam-injection temperature raised in this way increases the heat input, resulting in the improved efficiency of the gas-turbine. Based on the actual operation of the system, we obtained the following results: Operation with the steam-injection temperature at 300C (45C resuperheated from 255C) increased the efficiency of the gasturbine by 0.7%. The system can enhance the efficiency by 1.3% when the steam-injection temperature is elevated to 340C (85C resuperheated). In this case, up to 6.6 million yen of the total energy cost and 400 tons of carbon dioxide (CO2) emissions can be reduced annually. A gas-turbine cogeneration and RTO system can reduce energy consumption by 23% and CO2 emission by 30.1% at the plant.

Masaaki Bannai; Akira Houkabe; Masahiko Furukawa; Takao Kashiwagi; Atsushi Akisawa; Takuya Yoshida; Hiroyuki Yamada

2006-01-01T23:59:59.000Z

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High vacuum indirectly-heated rotary kiln for the removal and recovery of mercury from air pollution control scrubber waste  

SciTech Connect

SepraDyne corporation (Denton, TX, US) has conducted pilot-scale treatability studies of dewatered acid plant blowdown sludge generated by a copper smelter using its recently patented high temperature and high vacuum indirectly-heated rotary retort technology. This unique rotary kiln is capable of operating at internal temperatures up to 850 C with an internal pressure of 50 torr and eliminates the use of sweep gas to transport volatile substances out of the retort. By removing non-condensables such as oxygen and nitrogen at relatively low temperatures and coupling the process with a temperature ramp-up program and low temperature condensation, virtually all of the retort off-