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


1

Carbon Monoxide Safety Tips  

E-Print Network [OSTI]

Protect yourself and your family from the deadly effects of carbon monoxide--a colorless, odorless poisonous gas. This publication describes the warning signs of carbon monoxide exposure and includes a home safety checklist....

Shaw, Bryan W.; Garcia, Monica L.

1999-07-26T23:59:59.000Z

2

Carbon monoxide absorbing liquid  

SciTech Connect (OSTI)

The present disclosure is directed to a carbon monoxide absorbing liquid containing a cuprous ion, hydrochloric acid and titanum trichloride. Titanium trichloride is effective in increasing the carbon monoxide absorption quantity. Furthermore, titanium trichloride remarkably increases the oxygen resistance. Therefore, this absorbing liquid can be used continuously and for a long time.

Arikawa, Y.; Horigome, S.; Kanehori, K.; Katsumoto, M.

1981-07-07T23:59:59.000Z

3

SENSITIVE OPTOACOUSTIC DETECTION OF CARBON MONOXIDE BY RESONANCE ABSORPTION  

E-Print Network [OSTI]

Monoxide by Resonance Absorption Robert Gerlach and Nabil M.MONOXIDE BY RESONANCE ABSORPTION Robert Gerlach and Nabil M.the context of atmospheric absorption. The carbon monoxide

Gerlach, R.

2011-01-01T23:59:59.000Z

4

Why sequence carbon monoxide oxidizing thermophiles?  

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

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

5

Advanced Diesel Combustion with Low Hydrocarbon and Carbon Monoxide...  

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

Combustion with Low Hydrocarbon and Carbon Monoxide Emissions Advanced Diesel Combustion with Low Hydrocarbon and Carbon Monoxide Emissions Poster presented at the 16th Directions...

6

Desorption of carbon monoxide from nickel using mercaptans  

SciTech Connect (OSTI)

An IR spectroscopic study on the displacement of carbon monoxide with 1-propyl, 2-propyl-, 1-butyl-, 2-butyl-, and tert.-butyl mercaptan from nickel foil and silica-supported nickel showed that at low carbon monoxide coverage on supported nickel, mercaptan adsorption initially converted bridged to linear carbon monoxide surface species. At higher mercaptan pressures, carbon monoxide desorbed into the gas phase. A small amount of carbon monoxide remained on the surface when the poisoned sample was evacuated, and additional carbon monoxide adsorbed when 5 mm Hg of carbon monoxide was added to the evacuated sample.

Neff, L.D.; Sturdivant, A.E.; Wallace, J.L.

1980-06-01T23:59:59.000Z

7

Enhanced carbon monoxide utilization in methanation process  

DOE Patents [OSTI]

Carbon monoxide - containing gas streams are passed over a catalyst to deposit a surface layer of active surface carbon thereon essentially without the formation of inactive coke. The active carbon is subsequently reacted with steam or hydrogen to form methane. Surprisingly, hydrogen and water vapor present in the feed gas do not adversely affect CO utilization significantly, and such hydrogen actually results in a significant increase in CO utilization.

Elek, Louis F. (Peekskill, NY); Frost, Albert C. (Congers, NY)

1984-01-01T23:59:59.000Z

8

Carbon Monoxide Concentration Trends in Urban Atmospheres  

Science Journals Connector (OSTI)

...BOVE, J.L., AIRBORNE LEAD AND CARBON MONOXIDE...various procedures that release transmitter has been...conclusion for trans-mitter release. He also provided evidence...suburban counties, a larger fraction of the gasoline is undoubtedly...in the huts (indoor fires are used for space heating...

Merril Eisenbud; Laurel R. Ehrlich

1972-04-14T23:59:59.000Z

9

Isotopic equilibration of carbon monoxide catalyzed by supported ruthenium  

SciTech Connect (OSTI)

Isotopic equilibration of carbon monoxide catalyzed by supported ruthenium was studied with oxygen-18 and carbon-13 labeled carbon monoxide in the presence and absence of hydrogen. The results showed that carbon monoxide was present on commercial alumina-supported ruthenium in a reactive undissociated form at 373/sup 0/K; that it adsorbed as a single carbonyl and in a geminal dicarbonyl form; and that hydrogen inhibited the exchange reaction by competitive adsorption and by stabilizing the carbonyl bond. The results elucidate the carbon monoxide methanation and Fischer-Tropsch reactions on this catalyst.

Bossi, A. (Cent. Ric. Novara); Zanderighi, L.; Carnisio, G.; Garbassi, F.; Giunchi, G.; Petrini, G.

1980-09-01T23:59:59.000Z

10

Advanced Diesel Combustion with Low Hydrocarbon and Carbon Monoxide...  

Broader source: Energy.gov (indexed) [DOE]

Combustion with Low Hydrocarbon and Carbon Monoxide Emissions Poster Location P-19 Gregory K. Lilik, Andr L. Boehman Department of Energy & Mineral Engineering EMS Energy...

11

Mechanistical studies on the formation of carbon dioxide in extraterrestrial carbon monoxide ice analog samples  

E-Print Network [OSTI]

be produced via radiolysis of carbon monoxide ices.5 Indeed, the effects of ionizing radiation on pure carbonMechanistical studies on the formation of carbon dioxide in extraterrestrial carbon monoxide ice901220f Binary ice mixtures of two carbon monoxide isotopomers, 13 C16 O and 12 C18 O, were subjected

Kaiser, Ralf I.

12

CO (Carbon Monoxide Mixing Ratio System) Handbook  

SciTech Connect (OSTI)

The main function of the CO instrument is to provide continuous accurate measurements of carbon monoxide mixing ratio at the ARM SGP Central Facility (CF) 60-meter tower (36.607 °N, 97.489 °W, 314 meters above sea level). The essential feature of the control and data acquisition system is to record signals from a Thermo Electron 48C and periodically calibrate out zero and span drifts in the instrument using the combination of a CO scrubber and two concentrations of span gas (100 and 300 ppb CO in air). The system was deployed on May 25, 2005.

Biraud, S

2011-02-23T23:59:59.000Z

13

The Catalysis of the Carbon Monoxide-Steam Reaction  

Science Journals Connector (OSTI)

...The Catalysis of the Carbon Monoxide-Steam Reaction F. J. Long K. W. Sykes The kinetics of the carbon monoxide-steam reaction occurring heterogeneously at...nearly unity, while that with respect to steam is correspondingly lowered; a slight...

1952-01-01T23:59:59.000Z

14

E-Print Network 3.0 - ambient carbon monoxide Sample Search Results  

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

FACT SHEET Carbon monoxide (CO), known as the Invisible Killer... , propane, oil, wood, coal, and gasoline. Exposure to carbon monoxide can cause flu-like symptoms and can... .)...

15

Carbon and carbon monoxide hydrogenation on nickel: support effects  

SciTech Connect (OSTI)

Hydrogenation of carbon, deposited on nickel catalysts by CO disproportionation, was investigated by temperature-programmed surface reaction (TPSR) for four oxide supports, alumina (Al/sub 2/O/sub 3/), silica (SiO/sub 2/), titanium oxide (TiO/sub 2/), and SiO/sub 2/.Al/sub 2/O/sub 3/. The rate of carbon monoxide hydrogenation was measured by temperature-programmed reaction (TPR) for comparison. The rate of carbon hydrogenation to methane was found to be independent of the support and an average activation energy of 42 kJ/mol was estimated. In contrast, the rate of carbon monoxide hydrogenation was very sensitive to the catalyst support. Nickel (Ni) supported on TiO/sub 2/ exhibited the highest specific activity, and two distinct sites for methanation were observed on Ni/TiO/sub 2/ and Ni/Al/sub 2/O/sub 3/. The lowest specific activities were observed for Ni/SiO/sub 2/ and Ni/SiO/sub 2/.Al/sub 2/O/sub 3/. For all catalysts, carbon hydrogenation occurred at a lower temperature than carbon monoxide hydrogenation. For both TPR and TPSR, small amounts of ethane were formed and at a lower temperature than methane. The amount of less-active, ..beta..-carbon observed in TPSR experiments was very small on all catalysts. These results indicate that at high coverages, carbon hydrogenation does not depend on the support, and thus it is not rate-determining for CO hydrogenation in excess hydrogen. The support is also shown to change the specific rate of carbon monoxide methanation; activity differences seen in steady-state experiments are not just due to differences in site densities. 5 figures, 5 tables.

Ozdogan, S.Z.; Gochis, P.D.; Falconer, J.L.

1983-10-01T23:59:59.000Z

16

Process for producing carbon monoxide and hydrogen from methanol  

SciTech Connect (OSTI)

A process is described for producing carbon monoxide and hydrogen which comprises contacting methanol vapor at a temperature of 200 degrees to 300 degrees C with an indirectly heated zinc containing catalyst to obtain an effluent gas in which the components of carbon monoxide and hydrogen constitute at least 90% by volume of said gas. At least a part of the impurities from said effluent gas are removed and said effluent gas is deparated into its carbon monoxide and hydrogen components by adsorption. The effluent gas can be separated into its carbon monoxide and hydrogen components by use of a plurality of adsorbers containing zeolite-type molecular sieve material where the zeolite is substantially permeable to hydrogen but sorbs carbon monoxide.

Jockel, H.; Marschner, F.; Moller, F.W.; Mortel, H.

1982-02-23T23:59:59.000Z

17

Carbon monoxide exposure of subjects with documented cardiac arrhythmias  

SciTech Connect (OSTI)

The impact of low-level carbon monoxide exposure on ventricular arrhythmia frequency in patients with ischemic heart disease has not been thoroughly studied. The issue is of concern because of the potential proarrhythmic effect of carbon monoxide in patients with ischemic heart disease. We studied 30 subjects with well-documented coronary artery disease who had an average of at least 30 ventricular ectopic beats per hour over a 20-hour monitoring interval. By using appropriate inclusion and exclusion criteria, subjects were selected and enrolled in a randomized double-blind study to determine the effects of carbon monoxide exposure on ventricular arrhythmia frequency at rest, during exercise, and during ambulatory activities. The carbon monoxide exposure was designed to result in 3% or 5% carboxyhemoglobin levels, as measured by gas chromatography. The carbon monoxide exposure protocol produced target levels in 60 minutes, and the levels were maintained for an additional 90 minutes to provide adequate time to assess the impact of carbon monoxide on the frequency of ventricular ectopic beats. The data on total and repetitive ventricular arrhythmias were analyzed for seven specific time intervals: (1) two hours before carbon monoxide exposure; (2) during the two-hour carbon monoxide or air exposure; (3) during a two-hour rest period; (4) during an exercise period; (5) during an exercise recovery period; (6) six hours after carbon monoxide or air exposure; and (7) approximately 10 hours after exposure, or the remaining recording interval on the Holter monitor. There was no increase in ventricular arrhythmia frequency after carbon monoxide exposure, regardless of the level of carboxyhemoglobin or the type of activity.

Chaitman, B.R.; Dahms, T.E.; Byers, S.; Carroll, L.W.; Younis, L.T.; Wiens, R.D. (St. Louis Univ. School of Medicine, MO (United States))

1992-09-01T23:59:59.000Z

18

Comparison of Three CarbonComparison of Three Carbon Monoxide Databases in ConnecticutMonoxide Databases in Connecticut  

E-Print Network [OSTI]

Comparison of Three CarbonComparison of Three Carbon Monoxide Databases in ConnecticutMonoxide Databases in Connecticut Brian Toal, MSPHBrian Toal, MSPH Patricia Miskell, MPHPatricia Miskell, MPH Connecticut Department of Public HealthConnecticut Department of Public Health Environmental & Occupational

19

Reduction of Carbon Monoxide. Past Research Summary  

DOE R&D Accomplishments [OSTI]

Research programs for the year on the preparation, characterization, and reactions of binuclear tantalum complexes are described. All evidence to date suggest the following of these dimeric molecules: (1) the dimer does not break into monomers under mild conditions; (2) intermolecular hydride exchange is not negligible, but it is slow; (3) intermolecular non-ionic halide exchange is fast; (4) the ends of the dimers can rotate partially with respect to one another. The binuclear tantalum hydride complexes were found to react with carbon monoxide to give a molecule which is the only example of reduction of CO by a transition metal hydride to give a complex containing a CHO ligand. Isonitrides also reacted in a similar manner with dimeric tantalum hydride. (ATT)

Schrock, R. R.

1982-00-00T23:59:59.000Z

20

Carbon monoxide sensor and method of use thereof  

DOE Patents [OSTI]

Carbon monoxide sensors suitable for use in hydrogen feed streams and methods of use thereof are disclosed. The sensors are palladium metal/insulator/semiconductor (Pd-MIS) sensors which may possess a gate metal layer having uniform, Type 1, or non-uniform, Type 2, film morphology. Type 1 sensors display an increased sensor response in the presence of carbon monoxide while Type 2 sensors display a decreased response to carbon monoxide. The methods and sensors disclosed herein are particularly suitable for use in proton exchange membrane fuel cells (PEMFCs).

McDaniel; Anthony H. (Livermore, CA), Medlin; J. Will (Boulder, CO), Bastasz; Robert J. (Livermore, CA)

2007-09-04T23:59:59.000Z

Note: This page contains sample records for the topic "hc carbon monoxide" 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

Nickel and iron EXAFS of carbon monoxide dehydrogenase from Clostridium thermoaceticum strain DSM  

Science Journals Connector (OSTI)

Nickel and iron EXAFS of carbon monoxide dehydrogenase from Clostridium thermoaceticum strain DSM ...

Neil R. Bastian; Gabriele. Diekert; Eric C. Niederhoffer; Boon Keng. Teo; Christopher T. Walsh; William H. Orme-Johnson

1988-08-01T23:59:59.000Z

22

Carbon monoxide-assisted growth of carbon nanotubes Y.H. Tang a,b  

E-Print Network [OSTI]

Carbon monoxide-assisted growth of carbon nanotubes Y.H. Tang a,b , Y.F. Zheng a , C.S. Lee a , N was used to synthesize carbon nanotubes (CNTs) in a hot-®lament chemical vapor deposition (HFCVD) system in the formation of multi-walled carbon nanotubes (MWNT)s. The CNTs synthesized from carbon monoxide validate

Zheng, Yufeng

23

Carbon Monoxide Poisoning Avoided Through Weatherization | Department of  

Broader source: Energy.gov (indexed) [DOE]

Carbon Monoxide Poisoning Avoided Through Weatherization Carbon Monoxide Poisoning Avoided Through Weatherization Carbon Monoxide Poisoning Avoided Through Weatherization October 5, 2010 - 10:56am Addthis Joshua DeLung What does this mean for me? Getting your heating pipes fixed can not only save you money, but also improve your health. "If we'd had a couple cold nights where I would've had to use my heat more than usual, it probably would've put me to sleep and left me there -- it was just too much carbon monoxide coming out in the house," says Mark Pickartz, of Van Buren, Ark. Pickartz's home was weatherized in February by his local community action agency, Crawford-Sebastian Community Development Council (C-SCDC). When energy auditors arrived to his house, they found that his home's heater was severely leaking the poisonous gas. C-SCDC, based in Fort Smith, Ark.,

24

Carbon Monoxide Toxicity after Lighting Coals at a Hookah Bar  

Science Journals Connector (OSTI)

Unintentional non-fire-related (UNFR) carbon monoxide (CO) poisonings continue to account for a significant health and economic burden in the United States. While most of these poisonings are related to faulty...

Ryan Misek; Christine Patte

2014-09-01T23:59:59.000Z

25

Carbon monoxide-silicon carbide interaction in HTGR fuel particles  

Science Journals Connector (OSTI)

The corrosion of the coating-layers of silicon carbide (SiC) by carbon monoxide (CO) was observed in irradiated Triso-coated uranium dioxide particles, used in high-temperature gas-cooled reactors, by optical ...

Kazuo Minato; Toru Ogawa; Satoru Kashimura; Kousaku Fukuda…

1991-05-01T23:59:59.000Z

26

Titanium dioxide based high temperature carbon monoxide selective sensor  

E-Print Network [OSTI]

Titanium dioxide based high temperature carbon monoxide selective sensor Nancy O. Savagea , Sheikh as a trap for the oxidation products of CO and CH4. Upon oxidation of CO on ALC, carbonate species were detected, whereas the reaction of CH4 produced negligible carbonate species. The insensitivity of the ALC

Dutta, Prabir K.

27

Determination of the atherogenic potential of inhaled carbon monoxide  

SciTech Connect (OSTI)

he effects of chronic exposure to moderate levels of carbon monoxide upon the augmentation of arteriosclerotic plaque development were investigated in a series of in vivo studies in the cockerel (young rooster). This animal model has been well characterized, especially regarding the role of environmental agents in exacerbating early stages of plaque development. Cockerels injected with subtumorigenic doses of carcinogens exhibit markedly accelerated development of aortic arteriosclerotic plaques. Inhalation of mainstream smoke from two packs of cigarettes (100 minutes/day for 16 weeks) causes small but statistically significant increases in plaque size. As is the case with many animal models of plaque development, raised fat-proliferative plaques also appear in these animals following cholesterol feeding. Carbon monoxide is a ubiquitous pollutant in urban environments, where it is derived largely from mobile sources and cigarette smoke. Exposure to chronically elevated carbon monoxide levels has been implicated in a number of health-related problems. Whether such exposure plays a role in the development of arteriosclerosis has not been determined conclusively. In the present study, three questions were posed: 1. Will inhaled carbon monoxide at levels of 50 to 200 parts per million (ppm)* (two hours/day for 16 weeks) be sufficient to augment arteriosclerotic plaque development in cockerels, in the absence of other plaque-promoting agents 2. Will the inhalation of 100 ppm carbon monoxide (two hours/day for 16 weeks), concomitant with the feeding of low levels (0.1%) of cholesterol, yield larger plaques than those obtained with either of these agents administered alone 3. Will inhalation of 100 ppm carbon monoxide (two hours/day for 11 or 22 weeks), by cockerels in whom plaques have already appeared, further augment plaque development Cockerels were exposed to carefully regulated levels of carbon monoxide in stainless-steel and Plexiglas dynamic exposure chambers.

Penn, A. (New York Univ. Medical Center, NY (United States))

1993-05-01T23:59:59.000Z

28

Carbon Monoxide, Ozone, Hydrocarbon Air Quality Standards, and Related  

Broader source: Energy.gov (indexed) [DOE]

Monoxide, Ozone, Hydrocarbon Air Quality Standards, and Monoxide, Ozone, Hydrocarbon Air Quality Standards, and Related Emission Requirements (Ohio) Carbon Monoxide, Ozone, Hydrocarbon Air Quality Standards, and Related Emission Requirements (Ohio) < Back Eligibility Agricultural Commercial Construction Fuel Distributor Industrial Institutional Investor-Owned Utility Local Government Municipal/Public Utility Rural Electric Cooperative State/Provincial Govt Transportation Tribal Government Utility Savings Category Buying & Making Electricity Program Info State Ohio Program Type Environmental Regulations Provider Ohio Environmental Protection Agency This chapter defining the roles of the Ohio Environmental Protection Agency gives specific detail on the regulation point-source air pollution for a variety of industries and pollutants.

29

Disproportionation of carbon monoxide on supported nickel catalysts  

SciTech Connect (OSTI)

The disproportionation of carbon monoxide was investigated mainly on a 5.5% Ni/Al/sub 2/O/sub 3/ catalyst by infrared spectroscopy and temperature-programmed desorption. The reaction was found to be of first order with respect to the surface concentration of CO below 200/sup 0/C, while at 450/sup 0/C the reaction proceeded as a second order reaction for the pressure of CO. Results obtained with predeposited carbon indicated that the disproportionation reaction requires an ensemble of several nickel atoms. In agreement with this result, the disproportionation did not take place readily on a 1.1% Ni/Al/sub 2/O/sub 3/ catalyst on which a high dispersion of the metal was indicated by both infrared spectroscopy and the chemisorption of hydrogen. In the temperature-programmed desorption (TPD) carbon monoxide desorbed in a single peak before 300/sup 0/C. Some of the carbon monoxide, however, underwent disproportionation during TPD and a carbon dioxide peak appeared at about 220/sup 0/C. Furthermore, carbon thus deposited on the surface was oxidized to carbon monoxide by oxygen supplied from the catalysts and gave a second peak of CO in TPD at temperatures higher than 300/sup 0/C. Possible sources of the oxygen were discussed.

Galuszka, J.; Chang, J.R.; Amenomiya, Y.

1981-03-01T23:59:59.000Z

30

E-Print Network 3.0 - acute carbon monoxide Sample Search Results  

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

28, 2007 Summary: OSHAReproToxin AcutelyHazardousWaste Carbon monoxide CalOSHAReproToxin Carbon Tetrachloride IARC-2BNTP Carbonic... toxins, biotoxins and acutely toxic...

31

Kinetic model of catalytic oxidation of carbon monoxide on nickel  

SciTech Connect (OSTI)

A mechanism is proposed for describing the previous disclosed multiplicity of equilibrium states in the oxidation of carbon monoxide on metallic nickel. In contrast to the known mechanism for oxidation of CO on platinum metals it includes a nonlinear stage of carbon monoxide adsorption and a linear stage of oxygen adsorption. A kinetic model has been obtained and stage velocity constants have been found, providing a basis for obtaining a quantitative agreement between the calculated and experimental relations between the reaction velocity and the reagent concentrations. Opinions are stated in relation to the causes for evolution of the CO oxidation reaction from platinum metals to nickel.

Pyatnitskii, Yu.I.; Ostapyuk, V.A.

1986-07-01T23:59:59.000Z

32

Terpolymerization of ethylene, sulfur dioxide and carbon monoxide  

DOE Patents [OSTI]

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

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

1981-01-01T23:59:59.000Z

33

Photobiogeochemical cycling of carbon monoxide in the southeastern Beaufort Sea in spring and autumn  

E-Print Network [OSTI]

Photobiogeochemical cycling of carbon monoxide in the southeastern Beaufort Sea in spring the distribution, photoproduction, microbial uptake, and air­sea exchange of carbon monoxide (CO), a key that in warmer seas. Carbon monoxide (CO) is the dominant sink for hydroxyl radicals in the troposphere, thus

Vincent, Warwick F.

34

Infrared spectra of carbon monoxide adsorbed on palladium black  

SciTech Connect (OSTI)

The authors investigate the heterogeneous adsorption of carbon monoxide and the concurrent catalytic and sorptive properties of palladium black from the standpoint of a comprehensive analysis of the infrared spectra of the reaction pathways and their various products as well as the pressure dependence of the line behavior at various wavelengths.

Vozdvizhenskii, V.F.; Levintova, T.D.; Sokol'skii, D.V.

1986-06-01T23:59:59.000Z

35

Catalytic activation of carbon monoxide on metal surfaces  

SciTech Connect (OSTI)

In discussing the important basic aspects of carbon monoxide chemistry, this review covers the adsorption and reaction of CO with H/sub 2/O and H/sub 2/ on reduced metal surfaces. Carbon monoxide adsorption of the Group VIII metals exhibits certain patterns. Typically, as coverages exceed one-half, compression occurs in the monolayer and the molecules lose registry with the surface metal atoms. Particular sites associated with rough surfaces facilitate CO dissociation to the surface carbon; these sites may have a significant effect on selectivity in the CO hydrogenation reaction. The support used and the metal crystallite size both affect the catalyst activity and product selectivity. Indications are strong that a better knowledge of metal-support interactions combined with a more complete understanding of the surface chemistry involved will lead to improved catalyst systems in the future.

Vannice, M.A.

1982-01-01T23:59:59.000Z

36

Catalyst for the methanation of carbon monoxide in sour gas  

DOE Patents [OSTI]

The invention involves the synergistic effect of the specific catalytic constituents on a specific series of carriers for the methanation of carbon monoxide in the presence of sulfur at relatively high temperatures and at low steam to gas ratios in the range of 0.2:1 or less. This effect was obtained with catalysts comprising the mixed sulfides and oxides of nickel and chromium supported on carriers comprising magnesium aluminate and magnesium silicate. Conversion of carbon monoxide to methane was in the range of from 40 to 80%. Tests of this combination of metal oxides and sulfides on other carriers and tests of other metal oxides and sulfides on the same carrier produced a much lower level of conversion.

Kustes, William A. (Louisville, KY); Hausberger, Arthur L. (Louisville, KY)

1985-01-01T23:59:59.000Z

37

INFRARED ABSORPTION SPECTROSCOPY OF CARBON MONOXIDE ON NICKEL FILMS: A LOW TEMPERATURE THERMAL DETECTION TECHNIQUE  

E-Print Network [OSTI]

A. B. Optical System Absorption Signal C. Small SignalNoise . Sensitivity of Absorption Spectroscopy EXPERIMENTSINFRARED ABSORPTION SPECTROSCOPY OF CARBON MONOXIDE ON

Bailey, Robert Brian

2011-01-01T23:59:59.000Z

38

Carbon Monoxide Oxidation by Bacteria Associated with the Roots of Freshwater Macrophytes  

Science Journals Connector (OSTI)

...consumption and production of atmospheric carbon monoxide by...the consumption of atmospheric carbon monoxide by...rapid oxidation of atmospheric CO to CO2 by soils...D. Influence of water table on carbon dioxide...rice fields and biogas generators: CH4, N2O, CO...

Jeremy J. Rich; G. M. King

1998-12-01T23:59:59.000Z

39

Population based exposure assessment methodology for carbon monoxide: Development of a Carbon Monoxide Passive Sampler and Occupational Dosimeter  

E-Print Network [OSTI]

Monoxide Poisoning from Propane- Fueled Forklifts." JournalMonoxide Poisoning from Propane- Fueled Fotklifts" Journalto the Indoor Use of Propane-Fueled Forklifts in Colorado

Apte, Michael G.

2010-01-01T23:59:59.000Z

40

Removal of carbon monoxide. Physical adsorption on natural and synthetic zeolites  

SciTech Connect (OSTI)

The utilization of natural zeolite materials in the elimination of polluting gases is investigated. Carbon monoxide pollution is emphasized because its concentration may reach dangerous levels in places such as vehicle tunnels, underground parking lots, etc. The elimination of carbon monoxide is also of interest in some industrial processes relating to the production of pure gases.

Alfani, F.; Greco, G. Jr.; Iroio, G.

1982-07-01T23:59:59.000Z

Note: This page contains sample records for the topic "hc carbon monoxide" 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

Submitted to the Annals of Applied Statistics INTERPOLATING FIELDS OF CARBON MONOXIDE  

E-Print Network [OSTI]

and transport. CO AMS 2000 subject classifications: Carbon monoxide; satellite data; Bayesian hierarchi- cal models; interpolation; data assimilation 1 imsart-aoas ver. 2007/04/13 file: COpaper.tex date: March 24Submitted to the Annals of Applied Statistics INTERPOLATING FIELDS OF CARBON MONOXIDE DATA USING

Nychka, Douglas

42

Interaction of carbon monoxide with supported platinum catalysts  

SciTech Connect (OSTI)

The interaction of carbon monoxide with Pt/..gamma..-Al/sub 2/O/sub 3/ containing 0.5-5% Pt by weight has been investigated by means of thermal desorption and IR spectroscopy. It has been shown that CO is adsorbed in three different forms, corresponding to the desorption temperature intervals 25-250/sup 0/C (I), and 250-700/sup 0/C (II), and 550-850/sup 0/C (III). In the adsorption of CO in the first two forms, the metal takes part (absorption band at 2080 cm/sup -1/), and also the support (1800, 1260, 1390, 1470, 1550, and 1640 cm/sup -1/). The adsorption in form III probably takes place on oxidized platinum centers with the formation of strong surface carbonate structures. High temperatures tend to increase the adsorption of CO in forms II and III.

Savel'eva, G.A.; Galeev, T.K.; Popova, N.M.; Vozdvizhenskii, V.F.; Mishchenko, V.M.

1982-04-01T23:59:59.000Z

43

Indoor air pollutants from unvented kerosene heater emissions in mobile homes: studies on particles, semivolatile organics, carbon monoxide, and mutagenicity  

Science Journals Connector (OSTI)

Indoor air pollutants from unvented kerosene heater emissions in mobile homes: studies on particles, semivolatile organics, carbon monoxide, and mutagenicity ...

Judy L. Mumford; Ron W. Williams; Debra B. Walsh; Robert M. Burton; David J. Svendsgaard; Jane C. Chuang; Virginia S. Houk; Joellen Lewtas

1991-10-01T23:59:59.000Z

44

Some observations on the kinetics of the hydrogenation of carbon monoxide  

SciTech Connect (OSTI)

For the hydrogenation of CO a positive order of hydrogen and a slightly negative or a zero order in carbon monoxide are generally reported. The negative (or zero) order in carbon monoxide is often explained by assuming a strong adsorption of carbon monoxide on the same sites as used by the hydrogen. It is then assumed that the surface is ''almost totally'' covered by carbon monoxide. From experiments in which the surface products on an unsupported cobalt catalyst after the reaction were stripped off by a hydrogen treatment it was concluded that more than 95% of the surface (as determined from the adsorption of carbon monoxide at room temperature) was covered by carbon-containing species. This paper illustrates that ''zero order in carbon monoxide'' can be obtained with much lower coverage of carbon-containing species in equilibrium with gas-phase carbon monoxide than indicated above. Equations for reaction rates are presented, and data is calculated on the fraction of the catalyst surface covered by active carbon-containing species when the reaction is zero order in CO. The results suggest that only a small fraction of the catalyst surface is actively engaged in the hydrogenation of CO. This further suggests that the low turnover frequencies found for the Fischer-Tropsch synthesis could be caused by a small number of sites which are active in the rate-determining step. (MWF)

Rautavuoma, A.O.I.; van der Baan, H.S.

1981-10-01T23:59:59.000Z

45

Influence of the electrode material on carbon monoxide adsorption and electroreduction in aqueous solutions  

SciTech Connect (OSTI)

Carbon monoxide electroreduction was studied at rotating disk electrodes made of different materials (Cu, Au, Zn, Cd; amalgamated Cu; Al, Ga, In, glassy carbon, Sn, Pb, Mo, Fe, Ni, and certain binary systems). Positive partial currents which are evidence for a direct electroreduction of CO have been observed only at Zn, Ga, and Cd. The observation that CO is less susceptible to electroreduction than carbon dioxide is explained by the stronger chemisorption of carbon monoxide on the electrodes.

Osetrova, N.V.; Vasil'ev, Yu.B.

1987-12-01T23:59:59.000Z

46

Reduction of carbon monoxide emissions with regenerative thermal oxidizers  

SciTech Connect (OSTI)

Regenerative thermal oxidizers (RTOs) have been extensively used for the control of volatile organic compound (VOC) emissions from various sources. However, very little information is available on the ability of RTOs to control carbon monoxide (CO) emissions. This paper presents the results of extensive tests conducted on two RTOs to determine their VOC and CO control efficiencies. The inlet gas stream to the RTOs includes VOC and CO concentrations as high as 2,000 ppm and 3,600 ppm, respectfully. The testing demonstrated that both RTOs were capable of controlling greater than 98% of both inlet VOCs and CO. While the destruction efficiencies within the combustion chambers exceeded 99.9%, direct leakage past valves accounted for the lower control efficiencies. The tests indicated that the overall VOC and CO control efficiencies of the RTOs may be limited by valve leakage. The design and permitting of a RTO should include conservative control estimates which account for possible valve leakage.

Firmin, S.M.; Lipke, S.; Baturay, A.

1996-09-01T23:59:59.000Z

47

Crystallographic Snapshots of Cyanide- and Water-Bound C-Clusters from Bifunctional Carbon Monoxide Dehydrogenase/Acetyl-CoA Synthase  

E-Print Network [OSTI]

Nickel-containing carbon monoxide dehydrogenases (CODHs) reversibly catalyze the oxidation of carbon monoxide to carbon dioxide and are of vital importance in the global carbon cycle. The unusual catalytic CODH C-cluster ...

Kung, Yan

48

Role of Microorganisms in the Consumption and Production of Atmospheric Carbon Monoxide by Soil  

Science Journals Connector (OSTI)

...Winzer. 1932. Uber die Bildung von Essigsaure bei der biologischen Umsetzung von Kohlenoxyd und Kohlensaure mit Wasserstoff zu Methan. Biochem. Z. 245:2-12. 14. Fuchs, G., U. Schnitker, and R. K. Thauer. 1974. Carbon monoxide...

Ralf Conrad; Wolfgang Seiler

1980-09-01T23:59:59.000Z

49

Production of carbon monoxide-free hydrogen and helium from a high-purity source  

DOE Patents [OSTI]

The invention provides vacuum swing adsorption processes that produce an essentially carbon monoxide-free hydrogen or helium gas stream from, respectively, a high-purity (e.g., pipeline grade) hydrogen or helium gas stream using one or two adsorber beds. By using physical adsorbents with high heats of nitrogen adsorption, intermediate heats of carbon monoxide adsorption, and low heats of hydrogen and helium adsorption, and by using vacuum purging and high feed stream pressures (e.g., pressures of as high as around 1,000 bar), pipeline grade hydrogen or helium can purified to produce essentially carbon monoxide -free hydrogen and helium, or carbon monoxide, nitrogen, and methane-free hydrogen and helium.

Golden, Timothy Christopher (Allentown, PA); Farris, Thomas Stephen (Bethlehem, PA)

2008-11-18T23:59:59.000Z

50

Quantum cascade laser-based carbon monoxide detection on a second time scale from human breath  

Science Journals Connector (OSTI)

We present three different detection schemes for measuring carbon monoxide (CO) in direct absorption using a thermoelectrically cooled, distributed-feedback pulsed quantum cascade (qc) laser operating between 217...

B.W.M. Moeskops; H. Naus; S.M. Cristescu; F.J.M. Harren

2006-03-01T23:59:59.000Z

51

Continuous Measurement of Carbon Monoxide Improves Combustion Efficiency of CO Boilers  

E-Print Network [OSTI]

CONTINUOUS MEASUREMENT OF CARBON MONOXIDE IMPROVES COMBUSTION EFFICIENCY OF CO BOILERS Russell L. Branham ana James J. Prichard Ashland Oil Company Catlettsburg, KY ABSTRACT The paper describes the application of in-situ flue gas CO... measurement in the operation of CO Boilers and details the steps needed to optimize combustion efficiency. INTRODUCTION In the petroleum industry, the efficient operation of a fluid-cata1ytic-cracking unit, produces gases rich in carbon monoxide...

Gilmour, W. A.; Pregler, D. N.; Branham, R. L.; Prichard, J. J.

1981-01-01T23:59:59.000Z

52

Reformer-pressure swing adsorption process for the production of carbon monoxide  

SciTech Connect (OSTI)

An improved process for the production of carbon monoxide by the steam reforming of hydrocarbons is described comprising: (a) catalytically reacting a fluid hydrocarbon feed stream with steam in a steam reformer; (b) passing the reformer effluent containing hydrogen, carbon monoxide and carbon dioxide from the steam reformer, without scrubbing to remove the carbon dioxide content thereof, to a pressure swing adsorption system having at least four adsorbent beds, each bed of which, on a cyclic basis, undergoes a processing sequence; (c) recycling the carbon dioxide-rich stream to the steam reformer for reaction with additional quantities of the hydrocarbon feed stream being passed to the stream reformer to form additional quantities of carbon monoxide and hydrogen, with product recovery being enhanced and the need for employing a carbon dioxide wash system being obviated.

Fuderer, A.

1988-02-23T23:59:59.000Z

53

Analysis of black carbon and carbon monoxide observed over the Indian Ocean: Implications for emissions and photochemistry  

E-Print Network [OSTI]

and known emission factors for black carbon (BC) from South Asia yields 0.7 Tg yrÃ?1 (upper limit of about 1 Global Change: Atmosphere (0315, 0325); KEYWORDS: Soot, black carbon, CO, emissions, India Citation of black carbon and carbon monoxide observed over the Indian Ocean: Implications for emissions

Dickerson, Russell R.

54

Coadsorption of hydrogen and ethylene, and carbon monoxide and ethylene on the Ru(001) surface  

SciTech Connect (OSTI)

A detailed investigation of the coadsorption of ethylene with both preadsorbed hydrogen and preadsorbed carbon monoxide on the Ru(001) surface is reported here. Both preadsorbed hydrogen and carbon monoxide reduce the saturation coverage of subsequently chemisorbed ethylene. The coadsorption of hydrogen with ethylene results in detectable hydrogenation of ethylene to ethane below 250 K, whereas no self-hydrogenation of ethylene to ethane is observed. High-resolution electron energy loss spectra show that ethylene coadsorbed with either hydrogen or carbon monoxide decomposes to ethylidyne (CCH/sub 3/) and acetylide (CCH), as it does on the clean surface. Carbon monoxide preadsorption enhances the stability of the ethylidyne such that it decomposes at approximately 420 K, rather than 355 K as on the initially clean Ru(001) surface. Preadsorbed carbon monoxide also reduces the ratio of ethylidyne to acetylide that is formed from ethylene, compared to the ratio observed from an equivalent coverage of ethylene on the clean surface; hydrogen preadsorption, on the other hand, increases this ratio.

Hills, M.M.; Parmeter, J.E.; Weinberg, W.H.

1986-11-12T23:59:59.000Z

55

Carbon monoxide annealed TiO2 nanotube array electrodes for efficient biosensor applications  

E-Print Network [OSTI]

Carbon monoxide annealed TiO2 nanotube array electrodes for efficient biosensor applications by anodic oxidation of titanium foil followed with O2 and CO annealing were employed as matrices consisted of Ti3+ defects with carbon-doping and exhibited well defined quasi-reversible cyclic voltammetric

Cao, Guozhong

56

An experimental investigation of the ignition properties of hydrogen and carbon monoxide  

E-Print Network [OSTI]

for syngas turbine applications S.M. Walton *, X. He, B.T. Zigler, M.S. Wooldridge Department of Mechanical of simulated syngas mixtures of hydrogen (H2), carbon monoxide (CO), oxygen (O2), nitrogen (N2), and carbon mechanism for H2 and CO. Ã? 2006 The Combustion Institute. Published by Elsevier Inc. All rights reserved

Wooldridge, Margaret S.

57

Factors Affecting the Efficiency of Carbon Monoxide Photoproduction in the St. Lawrence Estuarine System (Canada)  

Science Journals Connector (OSTI)

Factors Affecting the Efficiency of Carbon Monoxide Photoproduction in the St. Lawrence Estuarine System (Canada) ... The solar insolation-weighted mean apparent quantum yield of CO (?CO) decreased as much as fourfold with increasing salinity and showed a strong positive correlation with the dissolved organic carbon-specific absorption coefficient at 254 nm. ...

Yong Zhang; Huixiang Xie; Guohua Chen

2006-11-01T23:59:59.000Z

58

A population-based exposure assessment methodology for carbon monoxide: Development of a carbon monoxide passive sampler and occupational dosimeter  

SciTech Connect (OSTI)

Two devices, an occupational carbon monoxide (CO) dosimeter (LOCD), and an indoor air quality (IAQ) passive sampler were developed for use in population-based CO exposure assessment studies. CO exposure is a serious public health problem in the U.S., causing both morbidity and mortality (lifetime mortality risk approximately 10{sup -4}). Sparse data from population-based CO exposure assessments indicate that approximately 10% of the U.S. population is exposed to CO above the national ambient air quality standard. No CO exposure measurement technology is presently available for affordable population-based CO exposure assessment studies. The LOCD and IAQ Passive Sampler were tested in the laboratory and field. The palladium-molybdenum based CO sensor was designed into a compact diffusion tube sampler that can be worn. Time-weighted-average (TWA) CO exposure of the device is quantified by a simple spectrophotometric measurement. The LOCD and IAQ Passive Sampler were tested over an exposure range of 40 to 700 ppm-hours and 200 to 4200 ppm-hours, respectively. Both devices were capable of measuring precisely (relative standard deviation <20%), with low bias (<10%). The LOCD was screened for interferences by temperature, humidity, and organic and inorganic gases. Temperature effects were small in the range of 10{degrees}C to 30{degrees}C. Humidity effects were low between 20% and 90% RH. Ethylene (200 ppm) caused a positive interference and nitric oxide (50 ppm) caused a negative response without the presence of CO but not with CO.

Apte, M.G.

1997-09-01T23:59:59.000Z

59

Mechanism of methanol synthesis from carbon monoxide and hydrogen on copper catalysts  

SciTech Connect (OSTI)

The authors examine possible mechanisms of methanol synthesis from carbon monoxide and hydrogen on supported copper catalysts. Two broad categories of reaction mechanism can be identified: (a) Type I: Carbon monoxide, adsorbed on the copper surface, is hydrogenated by the addition of hydrogen atoms while the C-O bond remains intact. A second C-O bond is neither formed nor broken. (b) Type II: Carbon monoxide (or a partially hydrogenated intermediate, e.g., HCO) reacts with an oxygen atom on the catalyst surface to give an intermediate, typically a formate, which contains two C-O bonds. Subsequent reaction leads overall to methanol and the reformation of the surface oxygen atom. Both mechanisms are discussed.

Fakley, M.E.; Jennings, J.R.; Spencer, M.S. (ICI Chemicals and Polymers Ltd, Billingham, Cleveland (England))

1989-08-01T23:59:59.000Z

60

Process for producing methane from gas streams containing carbon monoxide and hydrogen  

DOE Patents [OSTI]

Carbon monoxide-containing gas streams are passed over a catalyst capable of catalyzing the disproportionation of carbon monoxide so as to deposit a surface layer of active surface carbon on the catalyst essentially without formation of inactive coke thereon. The surface layer is contacted with steam and is thus converted to methane and CO.sub.2, from which a relatively pure methane product may be obtained. While carbon monoxide-containing gas streams having hydrogen or water present therein can be used only the carbon monoxide available after reaction with said hydrogen or water is decomposed to form said active surface carbon. Although hydrogen or water will be converted, partially or completely, to methane that can be utilized in a combustion zone to generate heat for steam production or other energy recovery purposes, said hydrogen is selectively removed from a CO--H.sub.2 -containing feed stream by partial oxidation thereof prior to disproportionation of the CO content of said stream.

Frost, Albert C. (Congers, NY)

1980-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "hc carbon monoxide" 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

Carbon monoxide oxidation on Rh(111): Velocity and angular distributions of the CO2 product  

E-Print Network [OSTI]

Carbon monoxide oxidation on Rh(111): Velocity and angular distributions of the CO2 product J. I and angular distributions of CO2 produced by CO oxidation on Rh 111 have been measured as a function a fundamental and a practical point of view. CO2 formation serves as a model recombina- tion reaction

Sibener, Steven

62

Observations of rotating jets of carbon monoxide in comet Hale-Bopp with the IRAM interferometer  

E-Print Network [OSTI]

Observations of rotating jets of carbon monoxide in comet Hale-Bopp with the IRAM interferometer;eres, France Abstract. CO was observed on March 11, 1997 in comet Hale-Bopp with the IRAM Plateau de for parent molecules. We have developed a 3-D model simulating rotating spiral jets of CO gas. We present

Demoulin, Pascal

63

Crystallization and mutational studies of carbon monoxide dehydrogenase from moorella thermoacetica  

E-Print Network [OSTI]

Carbon Monoxide Dehydrogenase (CODH), also known as Acetyl-CoA synthase (ACS), is one of seven known Ni containing enzymes. CODH/ACS is a bifunctional enzyme which oxidizes CO to CO2 reversibly and synthesizes acetyl-CoA. Recently, X-ray crystal...

Kim, Eun Jin

2004-09-30T23:59:59.000Z

64

Effect of redox potential, sulfide ions and a persulfide forming cysteine residue on carbon monoxide dehydrogenase  

E-Print Network [OSTI]

The Ni-Fe-S C-cluster of carbon monoxide dehydrogenases (CODH), which catalyzes the reversible oxidation of CO to CO2, can be stabilized in four redox states: Cox, Cred1, Cint, and Cred2. The best-supported mechanism of catalysis involves a one...

Feng, Jian

2005-08-29T23:59:59.000Z

65

Study of hydrogen and carbon monoxide adsorption on modified Zn/Cr catalysts by adsorption calorimetry  

SciTech Connect (OSTI)

Differential heat of adsorption (q) of hydrogen (a) and carbon monoxide (b) as a function of the adsorbed amount (a) on Zn/Cr catalysts at 463/sup 0/K; 1) unpromoted catalyst, 2) catalyst promoted with 2.5% of K/sub 2/O.

Yoshin, S.V.; Klyacho, A.L.; Kondrat'ev, L.T.; Leonov, V.E.; Skripchenko, G.B.; Sushchaya, L.E.

1986-08-01T23:59:59.000Z

66

Association of hydrogen metabolism with unitrophic or mixotrophic growth of Methanosarcina barkeri on carbon monoxide.  

Science Journals Connector (OSTI)

...by the simultaneous consumption of methanol and CO...by the simultaneous consumption of methanol and CO...conbustion of fossil fuels. Carbon monoxide is...involves the production and consumption of a carbonyl group...served as experi- mental vessels. Immediately after...

J M O'Brien; R H Wolkin; T T Moench; J B Morgan; J G Zeikus

1984-04-01T23:59:59.000Z

67

Electrochemical Removal of Carbon Monoxide in Reformate Hydrogen for Fueling Proton Exchange Membrane  

E-Print Network [OSTI]

Electrochemical Removal of Carbon Monoxide in Reformate Hydrogen for Fueling Proton Exchange Membrane Fuel Cells Sivagaminathan Balasubramanian, Charles E. Holland,* and John W. Weidner*,z Center in reformate hydrogen. In this design, the potential and gas flow are switched between the two filter cells so

Weidner, John W.

68

Molten metal reactor and method of forming hydrogen, carbon monoxide and carbon dioxide using the molten alkaline metal reactor  

DOE Patents [OSTI]

A molten metal reactor for converting a carbon material and steam into a gas comprising hydrogen, carbon monoxide, and carbon dioxide is disclosed. The reactor includes an interior crucible having a portion contained within an exterior crucible. The interior crucible includes an inlet and an outlet; the outlet leads to the exterior crucible and may comprise a diffuser. The exterior crucible may contain a molten alkaline metal compound. Contained between the exterior crucible and the interior crucible is at least one baffle.

Bingham, Dennis N.; Klingler, Kerry M.; Turner, Terry D.; Wilding, Bruce M.

2012-11-13T23:59:59.000Z

69

Carbon Monoxide Tolerant Electrocatalyst with Low Platinum Loading...  

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

particle. When used as an electrocatalyst for the oxidation of fuel at a fuel cell anode, this structure exhibits low platinum loading and elevated tolerance to carbon...

70

Impact of emissions, chemistry, and climate on atmospheric carbon monoxide : 100-year predictions from a global chemistry-climate model  

E-Print Network [OSTI]

The possible trends for atmospheric carbon monoxide in the next 100 yr have been illustrated using a coupled atmospheric chemistry and climate model driven by emissions predicted by a global economic development model. ...

Wang, Chien.; Prinn, Ronald G.

71

Relative and kinetic properties of carbon monoxide and carbon dioxide on a graphite surface  

SciTech Connect (OSTI)

Temperature-programmed desorption (TPD) results after chemisorption of carbon monoxide (CO) and carbon dioxide (CO/sub 2/) on polycrystalline graphite are presented. CO adsorbs onto graphite with a very low sticking coefficient. After CO chemisorption CO (mass 28 amu) desorbs in two temperature regions, between 400 and 700 K and between 1000 and 1300 K, and CO/sub 2/ (mass 44 amu) desorbs below 950 K. The intensity of the CO/sub 2/ signal is less than 1 order of magnitude lower than the CO intensity. After CO/sub 2/ adsorption the major desorption product is CO at high temperatures (1000 < T (K) < 1300), whereas a small amount of CO/sub 2/ desorbs around 450 K. The adsorption of C/sup 16/O/sub 2/ and C/sup 18/O/sub 2/ mixture leads to a nearly total oxygen scrambling of the CO/sub 2/ desorbed. A mechanism for CO and CO/sub 2/ interconversion on the graphite surface is presented in terms of surface oxide species, mainly lactones and semiquinones, and their relative stability. Assignments of the TPD features are proposed accordingly. Reaction studies on the CO/sub 2/ gasification of clean graphite and the CO disproportionation (Boudouard reaction) have been performed. A good agreement is found between the activation energies obtained and the desorption energies calculated from the analysis of the TPD results.

Marchon, B.; Tysoe, W.T.; Carrazza, J.; Heinemann, H.; Somorjai, G.A.

1988-10-06T23:59:59.000Z

72

Catalytic reactions on well-characterized vanadium oxide catalysts. 1. Oxidation of carbon monoxide  

SciTech Connect (OSTI)

The oxidation of carbon monoxide over unsupported and supported vanadium oxide catalysts was investigated from the standpoint of structure sensitivity. The activity of unsupported V/sub 2/O/sub 5/ markedly decreased the turnover frequency, while the reduction-oxidation treatment of the fused catalyst increased it. The turnover frequency of V/sub 2/O/sub 5//TiO/sub 2/ with low V/sub 2/O/sub 5/ content was much smaller than that of the V/sub 2/O/sub 5//TiO/sub 2/ with high V/sub 2/O/sub 5/ content or the unsupported V/sub 2/O/sub 5/. Such a retarding effect of the TiO/sub 2/ support on the activity of the oxidation of carbon monoxide is in contrast to the known promoting effect of TiO/sub 2/ for the oxidations of various hydrocarbons. From these results coupled with the characterization of the catalysts, it was concluded that the oxidation of carbon monoxide on vanadium oxide catalysts is a structure-sensitive reaction and that the activity of surface defects such as steps, kinks, and vacancies is much higher than that of the surface V=O species in the smooth (010) face of V/sub 2/O/sub 5/. 39 references, 9 figures, 2 tables.

Mori, K.; Miyamoto, A.; Murakami, Y.

1984-06-21T23:59:59.000Z

73

Gravimetric study of adsorbed intermediates in methanation of carbon monoxide  

SciTech Connect (OSTI)

The purpose of this study is to more fully elucidate the adsorbed intermediates and mechanism involved in catalytic methanation of CO on a typical nickel methanation catalyst. Rates of adsorption and desorption of surface species and of gasification of carbon were measured gravimetrically to determine their kinetics and possible roles in methanation. 19 refs.

Gardner, D.C.; Bartholomew, C.H.

1981-08-01T23:59:59.000Z

74

Mechanism of iron catalysis of carbon monoxide decomposition in refractories  

SciTech Connect (OSTI)

The authors discuss the catalytic effects of selected iron phases (metals, oxides, sulfides, and carbides) on the Boudouard reaction studied in an effort to more fully understand the disintegration of refractories when exposed to CO for long periods of time. It was found that active Fe atoms generated from the reduction of the iron oxides, especially {alpha}-Fe/sub 2/O/sub 3/, are the actual catalysts for the Boudouard reaction. The catalytic process confirmed by thermodynamic calculations, kinetic data, and X-ray diffraction data, consists of adsorption and decomposition of CO simultaneously forming carbides of iron. The chemisorption and subsequent decomposition of the iron carbides, rather than diffusion, constitute the rate-controlling process for carbon deposition.

Xu, M.W.P.; Brown, J.J. Jr. (Virginia Polytechnic Inst. and State Univ., Blacksburg, VA (USA). Dept. of Materials Engineering)

1989-01-01T23:59:59.000Z

75

Adsorption and desorption of hydrogen and carbon monoxide were studied on alumina-supported iridium catalysts  

SciTech Connect (OSTI)

The adsorption and desorption of hydrogen and carbon monoxide were studied on alumina-supported iridium catalysts which were examined by a scanning transmission electron microscope (STEM). The metal particle size and number of particles per area of catalyst increased with increasing metal loading. The particles were approx. 10 A. in diameter, cubo-octahedral shaped, and approx. 80-90% disperse. The STEM electron beam caused negligible damage to the samples. Hydrogen adsorption measurements showed that the hydrogen-iridium atom ratio was 1.2:1-1.3:1 and increased with decreasing metal loading. Temperature-programed desorption showed four types of adsorbed hydrogen desorbing at -90/sup 0/C (I), 15/sup 0/C (IV), 115/sup 0/C (II), and 245/sup 0/C (III). Types II and IV desorb from single atom sites and Types I and III from multiple atom sites. Type I is in rapid equilibrium with the gas phase. All desorption processes appear to be first order. Carbon monoxide adsorbed nondissociatively at 25/sup 0/C with approx. 0.7:1 CO/Ir atom ratio. It adsorbed primarily in linear forms at low coverage, but a bridged form appeared at high coverage.

Etherton, B.P.

1980-01-01T23:59:59.000Z

76

Ultraviolet photoelectron spectroscopic study of the interaction of potassium with carbon monoxide and benzene on the Pt(111) surface  

SciTech Connect (OSTI)

The interaction of potassium with carbon monoxide and benezene has been studied on the Pt(111) crystal surface by ultraviolet photoelectron spectroscopy (UPS). The adsorptive changes reported in previous studies for carbon monoxide and benzene when potassium is coadsorbed are correlated with the UPS results presented here and are explained with the aid of a molecular orbital analysis. The authors find that the valence molecular orbitals increase their binding energy slightly when the potassium is coadsorbed, implying a model in which the adsorbates sense the potassium-induced changes in dipole field at the surface. 36 references, 11 figures.

Kudo, M.; Garfunkel, E.L.; Somorjai, G.A.

1985-07-18T23:59:59.000Z

77

Observation of two-dimensional compositional ordering of a carbon monoxide and argon monolayer mixture physisorbed on graphite  

SciTech Connect (OSTI)

Commensurate monolayers of a mixture of 70% carbon monoxide and 30% argon on graphite are studied by neutron and low-energy-electron diffraction. A 2 x 2 superstructure due to 3:1 compositional ordering is observed below 25 K. The compositional ordering is most likely due to molecular-axis ordering of carbon monoxide molecules into a pinwheel pattern with argon atoms at the central sites of each pinwheel. Such a pinwheel structure has been predicted by Harris, Mouritsen, and Berlinsky for planar rotors with anisotropic interactions on a triangular lattice with vacancies.

You, H.; Fain, S.C. Jr.; Satija, S.; Passell, L.

1986-01-20T23:59:59.000Z

78

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

Science Journals Connector (OSTI)

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

Ana Pinheiro; Nathalie Dupassieux; Damien Hudebine; Christophe Geantet

2011-01-18T23:59:59.000Z

79

Design and Development of a Mid-Infrared Carbon Monoxide Sensor for a High-Pressure Combustor Rig  

E-Print Network [OSTI]

A sensor for carbon monoxide measurement has been developed using a mid-infrared quantum-cascade (QC) laser operating in the fundamental band (?v= 1) of CO near 4.5 ?m. The fundamental band was chosen due to its stronger absorption line...

Camou, Alejandro

2014-05-03T23:59:59.000Z

80

Chemisorption of carbon monoxide and nitrogen oxides on highly dispersed technetium  

SciTech Connect (OSTI)

The purpose of this work is to study, in infrared spectroscopy, the surface compounds formed on adsorption of carbon monoxide and nitrogen oxides on Tc/SiO/sub 2/. The samples were prepared by soaking Aerosil with aqueous solution of ammonium pertechnetate containing 10 wt.% of Tc. Reduction with hydrogen to the metal was carried out at 700-800/sup 0/C. Results indicated that chemisorption of CO on highly dispersed technetium gives rise to a single type of linear and several types of multicentered adsorption forms. Occurrence of bridge form of adsorbed CO was also suggested on the basis of the data on chemisorption stoichiometry. Formation of a structure characterizable by absorption at 1790 cm/sup -1/ may indicate, only after protracted analysis, that the surface of the technetium introduced gradually suffers significant rearrangement facilitating formation of this type of complexes.

Serebryakova, N.V.; Sokolova, N.P.; Spitsyn, V.S.

1982-08-01T23:59:59.000Z

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


81

Transformation of carbon monoxide dimer surface structures on yttrium oxide modified by silver  

SciTech Connect (OSTI)

It has been established that introducing ions of silver(II) in yttrium(III) oxide leads to the formation of a significant concentration of a paramagnetic dimer species (CO)/sub 2/-in the course of the adsorption of carbon monoxide, and that these dimers exhibit high thermal stability and reactivity. Reactions are proposed for the formation of the dimer species (CO)/sub 2//sup 2 -/ and (CO)/sub 2//sup -/ on the surface of the Ag/Y/sub 2/O/sub 3/ catalyst that involve the reduction of the anion vacancies and a change in the oxidation state of the silver ions. Modifying the yttrium oxide with ionic silver leads to a marked decrease in the strength of the oxidative ability of the surface of the catalyst for CO, while the nature of the active sites of the yttrium oxide, which adsorbs CO in three forms, remains unchanged.

Vydrin, S.N.; Bobolev, A.V.; Loginov, A.Yu.

1987-09-10T23:59:59.000Z

82

Infrared spectroscopic study of the adsorption of carbon monoxide on silica-supported copper oxide  

SciTech Connect (OSTI)

Adsorption of carbon monoxide at room temperature (0.1 to 50 Torr) on silica-supported copper oxide was studied by infrared spectroscopy. Catalysts were prepared by deposition-precipitation or impregnation. After calcination two types of adsorbed CO were identified showing absorption bands at 2136 +- 3 and 2204 +- 1 cm/sup -1/, which are ascribed to CO adsorbed on copper(II) oxide and on isolated copper(II) ions in the silica surface, respectively. Reduction and reoxidation removed the band at 2204 cm/sup -1/ with all samples and raised the intensity of the 2136-cm/sup -1/ band with the precipitated catalysts but not with the impregnation catalyst. Evidence is brought forward that the isolated copper ions are mobilized during reduction and generate new copper (oxide) surface. The change in background transmission of the samples could be used to obtain further information about the interaction of O/sub 2/ and CO with copper oxide.

De Jong, K.P.; Geus, J.W.; Joziasse, J.

1980-10-01T23:59:59.000Z

83

Modification of copper-chromium catalyst for steam conversion of carbon monoxide  

SciTech Connect (OSTI)

This paper presents the results of model tests that show that the copperchromium sample is superior in stability and activity to the industrial NTK-5 catalyst. Under unfavorable conditions with the use of industrial converted gas containing more than 20 vol.% of carbon monoxide, and with sulfur compounds, chlorine, and ammonia as impurities, after 3 months of continuous operation in the temperature range 190-260 degrees the catalyst lost less than 10% of inactivity (with respect to the degree of CO conversion), whereas the activity of the industrial NTK-4 catalyst fell by 15% under the same conditions. It is shown that a catalyst not inferior in properties to the industrial NTK-4 catalyst can be obtained by modifying the copper-chromium catalyst with aluminum compounds.

Khabibullin, R.R.; Torocheshnikov, N.S.

1986-08-01T23:59:59.000Z

84

Carbon monoxide adsorption/desorption processes over NaX zeolite and supported ruthenium catalyst  

SciTech Connect (OSTI)

The binding states of CO on NaX zeolite and RuNaX were investigated by thermal desorption spectroscopy. Desorption peaks centered at around 390, 430, 490, and 520 K were observed from NaX following room-temperature adsorption of CO. The activation energy values corresponding to these peaks were calculated to be 41.4, 45.7, 53.8, and 57.7 kJ mol{sup {minus}1}, respectively. These peaks were also observed in desorption profiles from RuNaX although their temperatures were higher by 10 to 20 K. In addition, the desorption spectra from RuNaX also comprise two high-temperature peaks at around 575 and 640 K. With both the RuNaX and the NaX samples the temperature and relative intensities of the desorption peaks depended on pretreatment conditions and on the lapsed time between CO exposure to the sample and the commencement of programmed heating. Mass spectral analysis revealed that the gas desorbed at 300-500 K consisted mainly of CO while at higher temperatures CO{sub 2} was the main component. The desorption peaks below 500 K are attributed to the release of carbon monoxide from structural and intragranular or intergranular zeolitic pores. Lewis sites on the zeolite surface are found to facilitate activation of CO, resulting in its transformation to CO{sub 2}. The initial adsorption of carbon monoxide in zeolite pores and subsequent diffusion to metal sites leading to its disproportionation/oxidation is found to play an important role in the CO adsorption/desorption process on RuNaX.

Kamble, V.S.; Gupta, N.M.; Iyer, R.M. (Bhabha Atomic Research Centre, Bombay (India))

1988-10-01T23:59:59.000Z

85

Effectiveness of Diesel Oxidation Catalyst in Reducing HC and CO Emissions from Reactivity Controlled Compression Ignition  

SciTech Connect (OSTI)

Reactivity Controlled Compression Ignition (RCCI) has been shown to allow for diesel-like or better brake thermal efficiency with significant reductions in nitrogen oxide (NOX) particulate matter (PM) emissions. Hydrocarbon (HC) and carbon monoxide (CO) emission levels, on the other hand, are similar to those of port fuel injected gasoline engines. The higher HC and CO emissions combined with the lower exhaust temperatures with RCCI operation present a challenge for current exhaust aftertreatments. The reduction of HC and CO emissions in a lean environment is typically achieved with an oxidation catalyst. In this work, several diesel oxidation catalysts (DOC) with different precious metal loadings were evaluated for effectiveness to control HC and CO emissions from RCCI combustion in a light-duty multi-cylinder engine operating on gasoline and diesel fuels. Each catalyst was evaluated in a steady-state engine operation with temperatures ranging from 160 to 260 C. A shift to a higher light-off temperature was observed during the RCCI operation. In addition to the steady-state experiments, the performances of the DOCs were evaluated during multi-mode engine operation by switching from diesel-like combustion at higher exhaust temperature and low HC/CO emissions to RCCI combustion at lower temperature and higher HC/CO emissions. High CO and HC emissions from RCCI generated an exotherm keeping the catalyst above the light-off temperature.

Prikhodko, Vitaly Y [ORNL; Curran, Scott [ORNL; Parks, II, James E [ORNL; Wagner, Robert M [ORNL

2013-01-01T23:59:59.000Z

86

Solar Carbon Monoxide, Thermal Profiling, and the Abundances of C, O, and their Isotopes  

E-Print Network [OSTI]

A solar photospheric "thermal profiling" analysis is presented, exploiting the infrared rovibrational bands of carbon monoxide (CO) as observed with the McMath-Pierce Fourier transform spectrometer (FTS) at Kitt Peak, and from above the Earth's atmosphere by the Shuttle-borne ATMOS experiment. Visible continuum intensities and center-limb behavior constrained the temperature profile of the deep photosphere, while CO center-limb behavior defined the thermal structure at higher altitudes. The oxygen abundance was self consistently determined from weak CO absorptions. Our analysis was meant to complement recent studies based on 3-D convection models which, among other things, have revised the historical solar oxygen (and carbon) abundance downward by a factor of nearly two; although in fact our conclusions do not support such a revision. Based on various considerations, an oxygen abundance of 700+/-100 ppm (parts per million relative to hydrogen) is recommended; the large uncertainty reflects the model sensitivity of CO. New solar isotopic ratios also are reported for 13C, 17O, and 18O.

Thomas R. Ayres; Claude Plymate; Christoph U. Keller

2006-06-07T23:59:59.000Z

87

Kinetics of the Reduction of Wüstite by Hydrogen and Carbon Monoxide for the Chemical Looping Production of Hydrogen  

E-Print Network [OSTI]

produced could be stored, e.g. by geological sequestration, making the overall process “carbon-neutral”, or “carbon-negative” when biomass is used as fuel. In addition, the hydrogen produced during the oxidation of FexO and metallic Fe in steam can be kept... Kinetics of the reduction of wüstite by hydrogen and carbon monoxide for the chemical looping production of hydrogen Wen Liu a,n, Jin Yang Lim b, Marco A. Saucedo a, Allan N. Hayhurst b, Stuart A. Scott a, J.S. Dennis b a Department of Engineering...

Liu, Wen; Lim, Jin Yang; Saucedo, Marco A.; Hayhurst, Allan N.; Scott, Stuart A.; Dennis, J. S.

2014-08-13T23:59:59.000Z

88

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

SciTech Connect (OSTI)

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

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

1988-11-10T23:59:59.000Z

89

Using the HP-41CV calculator as a data acquisition system for personal carbon monoxide exposure monitors  

SciTech Connect (OSTI)

The use of small, personal monitors as instruments for air pollution data acquisition, storage, and retrieval presents a new set of monitoring considerations. Portability, ruggedness, power supplies, and data capture are functions to be addressed in designing personal monitoring systems. The emphasis herein is on the data capture function. This paper describes experiences using the Hewlett-Packard HP-41CV system as a data management system interfaced with personal carbon monoxide monitors (General Electric Carbon Monoxide Detector, Model 15EC53CO3). In general, the HP-41CV proved to be reliable, adaptable, and easy to use. Problems with the monitor power source (battery failure) were more frequent than with the HP-41CV itself. Using the HP-41CV for the specific data collection requirements of the Washington Microenvironment Study is a focal point of this presentation.

Fitz-Simons, T.; Sauls, H.B.

1984-09-01T23:59:59.000Z

90

Total oxidation of carbon monoxide and methane over transition metal-fluorite oxide composite catalysts. I. Catalyst composition and activity  

SciTech Connect (OSTI)

A novel metal oxide composite catalyst for the total oxidation of carbon monoxide and methane was prepared by combining fluorite oxides with active transition metals. The fluorite oxides, such as ceria and zirconia, are oxygen-ion-conducting materials having catalytic properties usually at high temperatures. Active base metal catalysts, such as copper, were used as additives to promote the catalytic properties of these oxides. The contact of the two types of materials gave rise to a high active oxidation catalyst. At a space velocity of about 42,000 h{sup {minus}1}, complete carbon monoxide oxidation in air occurred at room temperature on the Au{sub 0.05}[Ce(La)]{sub 0.95}L{sub x} catalyst and at ca. 100{degrees}C on Cu-Ce-O composite catalysts. At the same space velocity, total oxidation of methane on the Cu-Ce-O catalyst doped with La{sub 2}O{sub 3} or SrO took place at ca. 550{degrees}C. The specific carbon monoxide oxidation activity of the Cu-Ce-O catalyst was several orders of magnitude higher than that of conventional copper-based catalysts and comparable or superior to platinum catalysts. This type of composite catalyst also showed excellent resistance to water vapor poisoning. The enhanced catalyst activity and stability resulted from strong interaction of the transition metal and fluorite oxide materials. 44 refs., 14 figs., 5 tabs.

Liu, W.; Flytzani-Stephanopoulos, F. [Tufts Univ., Medford, MA (United States)] [Tufts Univ., Medford, MA (United States)

1995-05-01T23:59:59.000Z

91

Adsorption of carbon monoxide on a smooth palladium electrode: an in-situ infrared spectroscopic study  

SciTech Connect (OSTI)

Adsorption of carbon monoxide on a smooth palladium electrode in 1 M HClO/sub 4/ saturated with CO was studied by two in-situ IR reflectance spectroscopic methods: EMIRS (electrochemically modulated infrared reflectance spectroscopy) and LPSIRS (linear potential sweep infrared reflectance spectroscopy). Two types of adsorbed CO, linear and bridged, were identified from the observed IR spectra, the latter being the predominant surface species. The C-O stretching frequency of the linear CO shifts to higher frequencies at more positive potentials with a slope of 48 cm/sup -1//V. The frequency of the bridged CO increases by 63 cm/sup -1/ between -0.5 and 0.9 V(NHE) and its integrated band intensity decreases continuously in the same potential region while the intensity of the linear CO is almost constant up to 0.1 V and then decreases gradually with increasing positive potential. The surface selection rule of the IR reflection absorption spectroscopy was tested for the present system by using the p- and s-polarized light. It was found that only p-polarized light gave the IR spectra of CO adsorbed on the palladium electrode thus proving the selection rule at the electrode/solution interface.

Kunimatsu, K.

1984-05-24T23:59:59.000Z

92

Cysteine 295 indirectly affects Ni coordination of carbon monoxide dehydrogenase-II C-cluster  

SciTech Connect (OSTI)

Highlights: •CODH-II harbors a unique [Ni-Fe-S] cluster. •We substituted the ligand residues of Cys{sup 295} and His{sup 261}. •Dramatic decreases in Ni content upon substitutions were observed. •All substitutions did not affect Fe-S clusters assembly. •CO oxidation activity was decreased by the substitutions. -- Abstract: A unique [Ni–Fe–S] cluster (C-cluster) constitutes the active center of Ni-containing carbon monoxide dehydrogenases (CODHs). His{sup 261}, which coordinates one of the Fe atoms with Cys{sup 295}, is suggested to be the only residue required for Ni coordination in the C-cluster. To evaluate the role of Cys{sup 295}, we constructed CODH-II variants. Ala substitution for the Cys{sup 295} substitution resulted in the decrease of Ni content and didn’t result in major change of Fe content. In addition, the substitution had no effect on the ability to assemble a full complement of [Fe–S] clusters. This strongly suggests Cys{sup 295} indirectly and His{sup 261} together affect Ni-coordination in the C-cluster.

Inoue, Takahiro; Takao, Kyosuke; Yoshida, Takashi [Division of Applied Biosciences, Graduate School of Agriculture, Kyoto University, Kyoto 606-8502 (Japan)] [Division of Applied Biosciences, Graduate School of Agriculture, Kyoto University, Kyoto 606-8502 (Japan); Wada, Kei [Organization for Promotion of Tenure Track, University of Miyazaki, Miyazaki 889-1692 (Japan)] [Organization for Promotion of Tenure Track, University of Miyazaki, Miyazaki 889-1692 (Japan); Daifuku, Takashi; Yoneda, Yasuko [Division of Applied Biosciences, Graduate School of Agriculture, Kyoto University, Kyoto 606-8502 (Japan)] [Division of Applied Biosciences, Graduate School of Agriculture, Kyoto University, Kyoto 606-8502 (Japan); Fukuyama, Keiichi [Department of Biological Sciences, Graduate School of Science, Osaka University, Toyonaka, Osaka 560-0043 (Japan)] [Department of Biological Sciences, Graduate School of Science, Osaka University, Toyonaka, Osaka 560-0043 (Japan); Sako, Yoshihiko, E-mail: sako@kais.kyoto-u.ac.jp [Division of Applied Biosciences, Graduate School of Agriculture, Kyoto University, Kyoto 606-8502 (Japan)] [Division of Applied Biosciences, Graduate School of Agriculture, Kyoto University, Kyoto 606-8502 (Japan)

2013-11-08T23:59:59.000Z

93

Carbon monoxide in the solar atmosphere I. Numerical method and two-dimensional models  

E-Print Network [OSTI]

The radiation hydrodynamic code CO5BOLD has been supplemented with the time-dependent treatment of chemical reaction networks. Advection of particle densities due to the hydrodynamic flow field is also included. The radiative transfer is treated frequency-independently, i.e. grey, so far. The upgraded code has been applied to two-dimensional simulations of carbon monoxide (CO) in the non-magnetic solar photosphere and low chromosphere. For this purpose a reaction network has been constructed, taking into account the reactions which are most important for the formation and dissociation of CO under the physical conditions of the solar atmosphere. The network has been strongly reduced to 27 reactions, involving the chemical species H, H2, C, O, CO, CH, OH, and a representative metal. The resulting CO number density is highest in the cool regions of the reversed granulation pattern at mid-photospheric heights and decreases strongly above. There, the CO abundance stays close to a value of 8.3 on the usual logarithmic abundance scale with [H]=12 but is reduced in hot shock waves which are a ubiquitous phenomenon of the model atmosphere. For comparison, the corresponding equilibrium densities have been calculated, based on the reaction network but also under assumption of instantaneous chemical equilibrium by applying the Rybicki & Hummer (RH) code by Uitenbroek (2001). Owing to the short chemical timescales, the assumption holds for a large fraction of the atmosphere, in particular the photosphere. In contrast, the CO number density deviates strongly from the corresponding equilibrium value in the vicinity of chromospheric shock waves. Simulations with altered reaction network clearly show that the formation channel via hydroxide (OH) is the most important one under the conditions of the solar atmosphere.

S. Wedemeyer-Boehm; I. Kamp; J. Bruls; B. Freytag

2005-03-23T23:59:59.000Z

94

Novel Carbon Monoxide Sensor for PEM Fuel Cell Systems C.T. Holt, A.-M. Azad, S.L. Swartz, W.J. Dawson, and P.K. Dutta  

E-Print Network [OSTI]

Novel Carbon Monoxide Sensor for PEM Fuel Cell Systems C.T. Holt, A.-M. Azad, S.L. Swartz, W The importance of carbon monoxide sensors for automotive PEM fuel cell systems is illustrated by a schematic will protect the PEM fuel cell stack; detection of CO is extremely important because too much CO will poison

Azad, Abdul-Majeed

95

Interaction of copper oxides with reaction medium in heterogeneous catalytic oxidation of carbon monoxide by molecular oxygen. IV. IR spectroscopic study of carbon monoxide interaction with copper oxide surface  

SciTech Connect (OSTI)

An IR spectroscopic study has been made of the interaction of CO with CuO prepared in different ways, and the interaction of O/sub 2/ with carbon monoxide preadsorbed on CuO. A number of Cu/sup +/CO surface complexes have been detected (2114-2148 cm/sup -1/) with a heat of adsorption about 79.5-180 kJ/mole. From an analysis of the nature of these complexes, we have evaluated the processes taking place on the CuO surface when it interacts with CO and have compared the properties of massive CuO with those of CuO on oxide supports. The data are interpreted on the assumption that extended defects - dislocations - exist and play an important role, determining to a considerable degree the properties of the massive CuO in the reaction of CO oxidation.

Lokhov, Y.A.; Popovskii, V.V.; Sadykov, V.A.; Tikhov, S.F.

1985-08-01T23:59:59.000Z

96

J. Phys. Chem. 1994, 98, 11213-11219 11213 Vibrational Dynamics of Carbon Monoxide at the Active Site of Myoglobin: Picosecond  

E-Print Network [OSTI]

J. Phys. Chem. 1994, 98, 11213-11219 11213 Vibrational Dynamics of Carbon Monoxide at the Active Physics Laboratory, Stanford University, Stanford, Califomia 94305 Received: April 27, 1994: In Final Form at Urbana-Champaign. Deparlment of Chemistry, Sfanford University. Hansen ExperimentaJ Physics Laboratory

Fayer, Michael D.

97

Process for the production of hydrogen and carbonyl sulfide from hydrogen sulfide and carbon monoxide using a metal boride, nitride, carbide and/or silicide catalyst  

SciTech Connect (OSTI)

Hydrogen and carbonyl sulfide are produced by a process comprising contacting gaseous hydrogen sulfide with gaseous carbon monoxide in the presence of a metal boride, carbide, nitride and/or silicide catalyst, such as titanium carbide, vanadium boride, manganese nitride or molybdenum silicide.

McGuiggan, M.F.; Kuch, P.L.

1984-05-08T23:59:59.000Z

98

Resilience of gas-phase anharmonicity in the vibrational response of adsorbed carbon monoxide and breakdown under electrical conditions  

E-Print Network [OSTI]

In surface catalysis, the adsorption of carbon monoxide on transition-metal electrodes represents the prototype of strong chemisorption. Notwithstanding significant changes in the molecular orbitals of adsorbed CO, spectroscopic experiments highlight a close correlation between the adsorbate stretching frequency and equilibrium bond length for a wide range of adsorption geometries and substrate compositions. In this work, we study the origins of this correlation, commonly known as Badger's rule, by deconvoluting and examining contributions from the adsorption environment to the intramolecular potential using first-principles calculations. Noting that intramolecular anharmonicity is preserved upon CO chemisorption, we show that Badger's rule for adsorbed CO can be expressed solely in terms of the tabulated Herzberg spectroscopic constants of isolated CO. Moreover, although it had been previously established using finite-cluster models that Badger's rule is not affected by electrical conditions, we find here th...

Dabo, Ismaila

2012-01-01T23:59:59.000Z

99

Adsorbate effects on a mixed-valence compound: Carbon monoxide chemisorption on CeIr/sub 2/  

SciTech Connect (OSTI)

We have studied the effects of stoichiometry change and CO chemisorption on the surface electronic structure of the mixed-valence compound CeIr/sub 2/. We show that the surface iridium to cerium ratio can be varied by changing sample temperature while sputtering. Carbon monoxide is found to adsorb 80% molecularly on the surface and cause a mild surface oxidation which induces a shift of electron density into available cerium f orbitals. Peaks due to the 4sigma, 1..pi.., and 5sigma CO molecular orbitals appear at different binding energies than those due to molecular CO on the pure iridium surface. This binding-energy shift as well as the high percentage of molecular CO on the surface (CO adsorption on pure cerium is completely dissociative) points toward a surface which has lost much of the elemental character of its two constituents upon compound formation.

Lindquist, J.M.; Hemminger, J.C.; Lawrence, J.

1987-10-15T23:59:59.000Z

100

Auger electron spectroscopy, electron loss spectroscopy and low energy electron diffraction of oxygen and carbon monoxide adsorption of Pd films  

SciTech Connect (OSTI)

The adsorption of oxygen and carbon monoxide at room temperature on polycrystalline and (111) monocrystalline thin films of Pd vapor deposited on mice was investigated by AES, ELS, and LEED. The results show that adsorbate coverage depends strongly on surface microstructure, composition, and topography. Polycrystalline or Cl contaminated surfaces adsorb large amounts of the gases, while flat, monocrystalline surfaces will adsorb almost none. These results are quite different from those observed earlier using sputter etched and annealed bulk single cyrstals where adsorbate superlattices formed after rather low gaseous exposures. In the present work no superlattices were observed after exposures ranging up to several thousand langmuirs. The contradictory results obtained in the two cases are attributed to probable differences in surface microtopography and microstructure.

Vook, R.W.; De Cooman, B.C.; Vankar, V.D.

1983-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "hc carbon monoxide" 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

Remarkable catalytic activity of cobalt tetraphenylporphyrin modified on a titania for the oxidation of carbon monoxide below room temperature  

SciTech Connect (OSTI)

CoTPP on TiO/sub 2/-120s modified at 250 /sup 0/C under vacuum catalytically oxidized carbon monoxide rapidly with oxygen even at -79/sup 0/C. Its catalytic activity was incomparably higher than that of commercial Hopcalite. Comparison of its catalytic performance with those of the same catalyst or different TiO/sub 2/ supporting catalyst both evacuated at 200 /sup 0/C revealed unique features of the present catalyst in terms of its oxygen adsorption, the poisoning of adsorbed oxygen, and the insolubility of the complex in benzene. Both significant structural modification of the complex and its strong interaction with properly dehydrated TiO/sub 2/-120s brought about by evacuation at 250 /sup 0/C may induce such extraordinary activity. 14 references, 4 figures, 5 tables.

Mochida, I.; Iwai, Y.; Kamo, T.; Fujitsu, H.

1985-12-05T23:59:59.000Z

102

Adsorbate effects on a mixed-valence compound: carbon monoxide chemisorption on CeIr/sub 2/  

SciTech Connect (OSTI)

The authors studied the effects of stoichiometry change and CO chemisorption on the surface electronic structure of the mixed-valence compound CeIr/sub 2/. It is shown that the surface iridium to cerium ratio can be varied by changing sample temperature while sputtering. Carbon monoxide is found to adsorb 80% molecularly on the surface and cause a mild surface oxidation which induces a shift of electron density into available cerium f orbitals. Peaks due to the 4 sigma, 1 pi, and 5 sigma CO molecular orbitals appear at different binding energies than those due to molecular CO on the pure iridium surface. This binding-energy shift as well as the high percentage of molecular CO on the surface (CO adsorption on pure cerium is completely dissociative) points toward a surface which has lost much of the elemental character of its two constituents upon compound formation.

Lindquist, J.M.; Hemminger, J.C.

1987-10-15T23:59:59.000Z

103

E-Print Network 3.0 - accidental carbon monoxide Sample Search...  

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

Health Collection: Biology and Medicine 33 Assessing and Modeling Exposure to Indoor Air Pollution among Rural Women in Guatemala Summary: pollution exposures to carbon...

104

E-Print Network 3.0 - accelerates carbon monoxide Sample Search...  

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

Health Collection: Biology and Medicine 31 Assessing and Modeling Exposure to Indoor Air Pollution among Rural Women in Guatemala Summary: pollution exposures to carbon...

105

States of cobalt and iron in catalysts supported in TiO{sub 2} from data of diffuse reflectance IR spectra of adsorbed carbon monoxide  

SciTech Connect (OSTI)

The variations in the oxidation states of cobalt and iron atoms in pure and mixed Co- and Fe-containing catalysts supported on TiO{sub 2} as a function of the conditions in which the catalysts were prepared and preliminarily treated were studied by analysis of the IR spectra of carbon monoxide adsorbed on these catalysts. A mutual influence of the components was discovered; iron was found to promote reduction of cobalt.

Davydov, A.A. [G.K. Boreskov Inst. of Catalysis, Novosibirsk (Russian Federation); Coville, N. [Univ. of the Wiswatersrand Wits, Johannesburg (South Africa)

1995-10-01T23:59:59.000Z

106

Relation between surface adsorption states and emf in a solid electrolyte concentration cell during carbon monoxide oxidation on platinum studied by local current measurement  

SciTech Connect (OSTI)

The importance of measuring adsorption during surface catalysis has been emphasized often. This is true for the oxidation of carbon monoxide on a platinum surface. Surface adsorption states during the reaction under steady states can be learned from electromotive force (emf) measurement with appropriate assumptions. Two mechanisms for emf generation have been proposed, one is that only oxygen activity generates emf, the other is that both oxygen and CO adsorption generates emf.

Okamoto, H.; Kawamura, G.; Kudo, T.

1984-04-01T23:59:59.000Z

107

HC-NIDS  

Energy Science and Technology Software Center (OSTI)

003182WKSTN00 HC-NIDS: signatures and simulations for detecting cyber-attacks aiming to cause damage against cyber-physical energy systems  not yet decided 

108

Effect of the type of carrier on the properties of cobalt catalysts in the synthesis of aliphatic hydrocarbons from carbon monoxide and hydrogen  

SciTech Connect (OSTI)

The properties of catalysts used in the synthesis of hydrocarbons from CO and H/sub 2/ are determined to a significant degree by the carriers used in their preparation. This paper deals with a study of the effect of the type of carrier on the properties of cobalt-based catalysts in the synthesis of aliphatic hydrocarbons from CO and H/sub 2/. Co catalysts that are active in the synthesis of hydrocarbons from CO and H/sub 2/ are those on which the adsorption of H/sub 2/ exceeds 3.10/sup -2/ mmole/g Co and the adsorptin of carbon monoxide exceeds 7.10/sup -2/ mmole/g Co. Carbon monoxide and hydrogen are adsorbed on active catalysts in weakly bound forms. A mechanism is proposed for the formatin of an active center and the adsorption of carbon monoxide on Co-catalysts which includes the appearance of a partial positive charge on the cobalt atom.

Lapidus, A.L.; Jem, H.C.; Krylova, A.Y.

1983-04-10T23:59:59.000Z

109

Kinetics and mechanisms of interactions of nitrogen and carbon monoxide with liquid niobium  

SciTech Connect (OSTI)

The kinetics and mechanisms of interactions of N{sub 2} and CO with liquid niobium were investigated in the temperature range of 2,700 to 3,000 K in samples levitated in N{sub 2}/Ar and CO/Ar streams. The nitrogen absorption and desorption processes were found to be second-order with respect to nitrogen concentration, indicating that the rate controlling step is either the adsorption of nitrogen molecules on the liquid surface or dissociation of absorbed nitrogen molecules into adsorbed atoms. The carbon and oxygen dissolution in liquid niobium from CO gas is an exothermic process and the solubilities of carbon and oxygen (C{sub Ce}, C{sub Oe} in at%) are related to the temperature and the partial pressure of CO. The reaction CO {yields} (C) + (O) along with the evaporation of niobium oxide takes place during C and O dissolution, whereas C and O desorption occurs via CO evolution only.

Park, H.G.

1990-01-01T23:59:59.000Z

110

Catalysts for the production of hydrocarbons from carbon monoxide and water  

DOE Patents [OSTI]

A method of converting low H.sub.2 /CO ratio syngas to carbonaceous products comprising reacting the syngas with water or steam at 200.degree. to 350.degree. C. in the presence of a metal catalyst supported on zinc oxide. Hydrocarbons are produced with a catalyst selected from cobalt, nickel or ruthenium and alcohols are produced with a catalyst selected from palladium, platinium, ruthenium or copper on the zinc oxide support. The ratio of the reactants are such that for alcohols and saturated hydrocarbons: (2n+1).gtoreq.x.gtoreq.O and for olefinic hydrocarbons: 2n.gtoreq.x.gtoreq.O where n is the number of carbon atoms in the product and x is the molar amount of water in the reaction mixture.

Sapienza, Richard S. (Shoreham, NY); Slegeir, William A. (Hampton Bays, NY); Goldberg, Robert I. (Selden, NY)

1987-01-01T23:59:59.000Z

111

Catalysts for the production of hydrocarbons from carbon monoxide and water  

DOE Patents [OSTI]

A method of converting low H/sub 2//CO ratio syngas to carbonaceous products comprising reacting the syngas with water or steam at 200 to 350/sup 0/C in the presence of a metal catalyst supported on zinc oxide. Hydrocarbons are produced with a catalyst selected from cobalt, nickel or ruthenium and alcohols are produced with a catalyst selected from palladium, platinum, ruthenium or copper on the zinc oxide support. The ratio of the reactants are such that for alcohols and saturated hydrocarbons: (2n + 1) greater than or equal to x greater than or equal to O and for olefinic hydrocarbons: 2n greater than or equal to x greater than or equal to O where n is the number of carbon atoms in the product and x is the molar amount of water in the reaction mixture.

Sapienza, R.S.; Slegeir, W.A.; Goldberg, R.I.

1985-11-06T23:59:59.000Z

112

Carbon monoxide line emission as a CMB foreground: tomography of the star-forming universe with different spectral resolutions  

E-Print Network [OSTI]

The rotational lines of carbon monoxide and the fine structure lines of CII and of the most abundant metals, emitted during the epoch of enhanced star formation in the universe, are redshifted in the frequency channels where the present-day and future CMB experiments are sensitive. We estimate the contribution to the CMB angular power spectrum by the emission in such lines in merging star-forming galaxies. We used the Lacey-Cole approach to characterize the distribution of the merging halos, together with a parametrization for the star formation rate in each of them. Using observational data from a sample of local, low-redshift, and high-redshift objects, we calibrated the luminosity in each line as a function of the star formation rate. We show that the correlation term arising from CO line emission is a significant source of foreground for CMB in a broad range of frequencies (in particular in the 20-60 GHz band) and for 1000

Mattia Righi; Carlos Hernandez-Monteagudo; Rashid Sunyaev

2008-07-24T23:59:59.000Z

113

Photochemical generation of carbon monoxide and hydrogen by reduction of carbon dioxide and water under visible light irradiation  

Science Journals Connector (OSTI)

...energy conversion with consumption of a pollutant, CO2...energy conversion with consumption of a pollutant, CO...energy conversion with consumption of a pollutant, CO2...energy by producing fuels (hydrogen, carbon...M) in the reaction vessel; the gas contained...

Jean-Marie Lehn; Raymond Ziessel

1982-01-01T23:59:59.000Z

114

Higher energy electronic transitions of HC2n+1H+ ,,n=27... and HC2n+1H  

E-Print Network [OSTI]

Higher energy electronic transitions of HC2n+1H+ ,,n=2­7... and HC2n+1H ,,n=4­7... in neon matrices to other carbon chains. The B~ 3 u - X~ 3 g - transition in the UV of neutral HC2n+1H n=4­7 has also been, they are perhaps building blocks of larger organic sys- tems such as polycyclic aromatic hydrocarbons. CnH,4­7 Cn

Maier, John Paul

115

Infrared spectroscopic studies of carbon monoxide adsorbed on a series of silica-supported copper catalysts in different oxidation states  

SciTech Connect (OSTI)

Infrared spectroscopy has been used to study the adsorption of carbon monoxide (358-493 K, 0.1-20 kPa) on four copper-on-silica (2-10 wt% Cu) catalysts prepared by the ion-exchange technique. The measurements are made for each sample in three different states: unreduced (predominantly Cu{sup 2+}), and reduced (Cu{sup 0}), and partially reoxidized in nitrous oxide (Cu{sup +}). On unreduced samples, a major absorption band between 2127 and 2132 cm{sup {minus}1} due to CO adsorbed on small CuO particles and a weak band at 2199 cm{sup {minus}1} due to CO on isolated Cu{sup 2+} ions incorporated in the silica surface have been identified. The former adsorption obeys a Langmuir isotherm with a heat of adsorption of 29 kJ/mol independent of CuO particle size and surface coverage. After catalyst reduction, the major absorption band lies between 2090 and 2113 cm{sup {minus}1} and arises from CO linearly bound to very small (1- to 5-nm) copper metal clusters. The observed frequency shifts indicate the presence of steps and terraces similar to low index Cu planes in very small particles (1- to 2-nm), and the presence of similar higher index Cu planes on larger clusters (2- to 5-nm). The absorption is described by a Freundlich isotherm with the heat of CO adsorption decreasing with coverage from 50 to 22 kJ/mol on bigger particles but more constant (27 to 22 kJ/mol) on small particles. A surface copper/CO atomic ratio increasing from 5 to 12 is established at equilibrium saturation between 358 and 493 K using extinction coefficients determined in this study. In the reduced catalysts, a weakly adsorbed ({Delta}H{sub a} = {minus}20 kJ/mol) species assigned to CO bound to isolated Cu{sup +} ions is also found and absorbs at 2175 cm{sup {minus}1}. The frequency of this band does not vary with catalyst loading and is not affected by reoxidation of the catalyst in nitrous oxide.

Kohler, M.A.; Wainwright, M.S.; Trimm, D.L.; Cant, N.W. (Macquarie Univ., New South Wales (Australia) Univ. of South Wales (Australia))

1989-05-01T23:59:59.000Z

116

Infrared spectra of carbon monoxide adsorbed on SiO sub 2 -supported lanthanide-Ni bimetallic catalysts and their catalytic properties  

SciTech Connect (OSTI)

Recently the surface properties of the lanthanide (rare earth) - transition metal intermetallics and lanthanide metal overlayers have attracted a growing interest from the point of view of technical applications in catalyst and hydrogen storage. However, despite the intrinsic interest and considerable potential of these novel materials, very little detailed work has been carried out with a view to unveiling the specific properties upon interactions of lanthanides with transition metals. It has been shown that Eu and Yb metals dissolve in liquid ammonia to yield homogeneous solutions containing the ammoniated electrons. When the transition metal powders are added to this solution, the metal powders react with the dissolved lanthanide metals in liquid ammonia to form novel bimetallic catalysts. Such a system can be used as a catalyst probe for studying the catalytic actions induced by interactions between the lanthanide and transition metals. The present investigation was extended to include a SiO{sub 2}-supported bimetallic systems obtained when Eu or Yb dissolved in liquid ammonia reacts with silica-supported Ni. Using Fourier transform (FT)-IR studies of adsorbed carbon monoxide the authors provided information about the way the surface components were disposed in this bimetallic system. Adsorbed carbon monoxide was used as a molecular probe for the nature of bimetallic surface since the IR spectra of adsorbed probe molecules directly reflected variations in the surface.

Imamura, Hayao; Sugimoto, Hiromi; Sakata, Yoshihisa; Tsuchiya, Susumu (Yamaguchi Univ., Ube (Japan))

1992-07-01T23:59:59.000Z

117

Increased combustion rate of chlorobenzene on Pt/?-Al2O3 in binary mixtures with hydrocarbons and with carbon monoxide  

Science Journals Connector (OSTI)

The catalytic combustion of chlorobenzene on a 2 wt.% Pt/?-Al2O3 catalyst in binary mixtures with various hydrocarbons (toluene, benzene, cyclohexane, cyclohexene, 1,4-cyclohexadiene, 2-butene, and ethene) and with carbon monoxide has been explored. For all binary mixtures used the (excess of) added hydrocarbon increased the rate of conversion of chlorobenzene. With 2-butene, T50% and T100% for chlorobenzene were reduced by 100 and 200°C, respectively. Toluene and ethene were almost equally efficient as 2-butene. Co-feeding benzene or carbon monoxide resulted in a much smaller decrease of the T50%. The additional heat and water production in hydrocarbon combustion may contribute to some extent to the observed rate acceleration, but removal of Cl from the surface due to the hydrocarbon appears to be the major factor. The co-feeding of hydrocarbons invariably reduced the output of polychlorinated benzenes, which are formed as byproducts in the combustion of chlorobenzene on Pt/?-Al2O3. Again, especially toluene, ethene, and 2-butene were very efficient. Benzene — as well as cyclohexane, cyclohexene, and 1,4-cyclohexadiene, which were converted in situ into benzene — was much less effective, due to chlorination of the aromatic nucleus. In chlorobenzene–CO mixtures the levels of polychlorinated benzenes were almost as high as with chlorobenzene per se. Removal of Cl from the surface (mainly in the form of HCl) by (non-aromatic) hydrocarbons is responsible for reducing the formation of byproducts.

R.W. van den Brink; R. Louw; P. Mulder

2000-01-01T23:59:59.000Z

118

Final Technical Report "Catalytic Hydrogenation of Carbon Monoxide and Olefin Oxidation" Grant number : DE-FG02-86ER13615  

SciTech Connect (OSTI)

Title: Catalytic Hydrogenation of Carbon Monoxide and Olefin Oxidation Grant No. DE-FG02-86ER13615 PI: Wayland, B. B. (wayland@sas.upenn.edu) Abstract Development of new mechanistic strategies and catalyst materials for activation of CO, H2, CH4, C2H4, O2, and related substrates relevant to the conversion of carbon monoxide, alkanes, and alkenes to organic oxygenates are central objectives encompassed by this program. Design and synthesis of metal complexes that manifest reactivity patterns associated with potential pathways for the hydrogenation of carbon monoxide through metallo-formyl (M-CHO), dimetal ketone (M-C(O)-M), and dimetal dionyl (M-C(O)-C(O)-M) species is one major focus. Hydrocarbon oxidation using molecular oxygen is a central goal for methane activation and functionalization as well as regioselective oxidation of olefins. Discovery of new reactivity patterns and control of selectivity are pursued through designing new metal complexes and adjusting reaction conditions. Variation of reaction media promotes distinct reaction pathways that control both reaction rates and selectivities. Dimetalloradical diporphyrin complexes preorganize transition states for substrate reactions that involve two metal centers and manifest large rate increases over mono-metalloradical reactions of hydrogen, methane, and other small molecule substrates. Another broad goal and recurring theme of this program is to contribute to the thermodynamic database for a wide scope of organo-metal transformations in a range of reaction media. One of the most complete descriptions of equilibrium thermodynamics for organometallic reactions in water and methanol is emerging from the study of rhodium porphyrin substrate reactions in aqueous and alcoholic media. Water soluble group nine metalloporphyrins manifest remarkably versatile substrate reactivity in aqueous and alcoholic media which includes producing rhodium formyl (Rh-CHO) and hydroxy methyl (Rh-CH2OH) species. Exploratory directions for this program include expending new strategies for anti-Markovnikov addition of water, alcohols, and amines with olefins, developing catalytic reactions of CO to give formamides and formic esters, and evaluating the potential for coupling reactions of CO to produce organic building blocks.

Wayland, B.B.

2009-08-31T23:59:59.000Z

119

Quantum-chemical investigation of the interaction of nitrogen and carbon monoxide molecules with the Lewis acid sites of aluminium oxide  

SciTech Connect (OSTI)

Within the framework of the cluster approximation, using covalent and ionic models of Lewis acid sites of aluminumoxide, their electronic structure, as well as that of complexes of nitrogen and carbon monoxide molecules with them, was calculated. It was shown that the Lewis acid sites, representing a truncated tetrahedron, exhibit stronger electron-acceptor properties than the corresponding sites in the form of a truncated octahedron. For both molecules, the linear form of adsorption is energetically more profitable than the T-shaped form. The results obtained by the nonempirical SCF MO LCAO method in the STO-3GF basis and by semiempirical methods in CNDO/2 and INDO approximatations, are qualitatively the same.

Senchenya, I.N.; Chuvylkin, N.D.; Kazanskii, V.B.

1986-11-01T23:59:59.000Z

120

Studies on the sulfur poisoning of Ru-RuO{sub x}/TiO{sub 2} catalyst for the adsorption and methanation of carbon monoxide  

SciTech Connect (OSTI)

The effects of sulfur poisoning on the chemisorption and on the methanation of carbon monoxide over Ru/TiO{sub 2} catalyst were investigated by FTIR spectroscopy and volumetric gas adsorption measurements. The CS{sub 2} molecules are {eta}` bonded to Ru sites through one of the sulfur atoms and decompose to the constituent elements on thermal activation. Each S atom may deactivate 3 to 10 metal sites even at low coverages, the effect being more pronounced on the chemisorption of hydrogen. The deposited sulfur (and possibly carbon also) sterically hinders the formation of certain multicarbonyl and monocarbonyl species (vCO in 2055-2140 cm{sup -1} region), which otherwise transform to methane via surface methylene groups in the presence of chemisorbed hydrogen and are found to play an important role in the low-temperature methanation activity of the studied catalyst. The Ru-CO species giving rise to lower frequency vibrational bands are affected to a lesser extent. The presence of sulfur also results in the development of some new CO binding states which are weak and are identified with the CO and S coadsorbed at Ru sites of different oxidation states or of varying crystallographic nature. The CO adsorbed in these states is not reactive to hydrogen. 45 refs., 9 figs., 1 tab.

Kamble, V.S.; Londhe, V.P.; Gupta, N.M. [Bhambha Atomic Research centre, Bombay (India)] [and others] [Bhambha Atomic Research centre, Bombay (India); and others

1996-02-01T23:59:59.000Z

Note: This page contains sample records for the topic "hc carbon monoxide" 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

FTIR study of carbon monoxide oxidation and scrambling at room temperature over copper supported on ZnO and TiO{sub 2} No. 1  

SciTech Connect (OSTI)

An FTIR and quadrupole mass spectroscopic study of CO adsorption and oxidation with {sup 16}O{sub 2} and {sup 18}O{sub 2} on copper supported on ZnO and TiO{sub 2} is presented. The experimental results indicate that CO is adsorbed on the metallic particles dispersed on both oxides on two kinds of sites, on the normal terrace sites and on sites at the borderline of the particles. Moreover, on titania, a band at 2126 cm{sup -1}, assigned to CO adsorbed on isolated Cu atoms and/or on two-dimensional small clusters, is detected. A frequency shift of the bands of CO adsorbed on the metallic particles observed in the CO-O{sub 2} coadsorption experiments and the occurrence of a scrambling reaction between CO and {sup 18}O{sub 2} reveal that on all these samples, there are metallic sites which are able to adsorb at the same time oxygen atoms and carbon monoxide. Carbon dioxide and carbonate-like species are formed: the asymmetric stretching frequencies of CO{sub 2} and the quadrupole mass spectroscopic analysis reveal that with {sup 18}O{sub 2}, different isotopic molecular CO{sub 2}`s are formed, while the carbonate-like species have the same frequencies of those produced in {sup 16}O{sub 2}. Moreover, these species are completely lacking in the absence of oxygen in the gas phase. The experimental results indicate the there are, on these samples, two independent pathways for the CO oxidation, a direct oxidation of CO at the surface of the metallic particles and an induced oxidation with the surface lattice oxygen species of the supports. 46 refs., 8 figs.

Baccuzzi, F.; Chiorino, A. [Universita di Torino (Italy)] [Universita di Torino (Italy)

1996-02-29T23:59:59.000Z

122

Extending surface-enhanced Raman spectroscopy to transition-metal surfaces: carbon monoxide adsorption and electrooxidation on platinum- and palladium-coated gold electrodes  

SciTech Connect (OSTI)

Thin (ca. one to three monolayers) films of platinum and palladium electrodeposited on electrochemically roughened gold are observed to yield surface-enhanced Raman (SER) spectra for adsorbed carbon monoxide. The major vibrational band(s) on these surfaces are diagnosed from their frequencies as arising from C-O stretching vibrations, nu/sub CO/ bound to the transition-metal overlayers rather than to residual gold sites. The observed SFR nu/sub CO/ frequencies are closely similar to (within ca. 10 cm/sup -1/ of) those obtained for these systems from potential-difference infrared (PDIR) spectra. The major SERS and PDIR nu/sub CO/ features for the platinum and palladium surfaces appear at 2060-2090 and 1965-1985 cm/sup -1/, respectively, consistent with the presence of terminal and bridging CO on these two electrodes. The infrared as well as electrochemical properties of these systems are closely similar to those for the corresponding polycrystalline bulk electrodes. A difference between the SER- and IR-active adsorbed CO, however, is that the former undergoes electrooxidation on both surfaces at 0.2-0.3 V higher overpotentials than the latter form. Examination of the potential-dependent SERS bands for metal oxide vibrations, nu/sub PtO/, on the platinum surface shows that the electrooxidation potential for the SERS-active adsorbed CO coincides with that for the appearance of the nu/sub PtO/ band. Some broader implications to the utilization of SERS for examining transition-metal surfaces are pointed out.

Leung, L.W.H.; Weaver, M.J.

1987-08-19T23:59:59.000Z

123

Chemisorption and catalysis by metal clusters. II. Chemisorption of carbon monoxide and of oxygen by supported osmium clusters derived from Os/sub 3/(CO)/sub 12/ and from Os/sub 6/(CO)/sub 18/  

SciTech Connect (OSTI)

Carbon monoxide and oxygen have been chemisorbed at 293 K on the high-nuclearity carbonyl-protected clusters (the various species A) obtained by heating in vacuo to 523 K Os/sub 3/(CO)/sub 12/ or Os/sub 6/(CO)/sub 18/ impregnated on silica, alumina, or titania. The adsorption isotherms have a conventional appearance, but most are composed of a primary and a secondary region. Material adsorbed in the secondary region is removed by evacuation at room temperature whereas that adsorbed in the primary region is removed by evacuation at elevated temperatures. For species A/alumina and the species A/titania the primary region is complete and the secondary region commences when the pressure over the adsorbent is 0.2 Torr. Species A/silica gave no secondary region in oxygen adsorption. Adsorption and subsequent temperature-programmed desorption of (/sup 18/O)CO occurred without any dilution by (/sup 16/O)CO, indicating that ligand-(/sup 16/O)CO and adsorbed-(/sup 18/O)CO do not exchange even at elevated temperatures. The two species A/aluminas catalyzed oxygen isotope exchange at 293 K. From the experimental evidence it is deduced that carbon monoxide and oxygen each adsorbs molecularly in both the primary and the secondary regions. In the primary region carbon monoxide adsorption occurs at osmium sites on the cluster framework, whereas in the secondary region it occurs at ligand-carbon bonded to osmium. For oxygen, adsorption in the primary region is again at osmium sites on the cluster framework but that in the secondary region is at osmium sites of the cluster framework suitably modified as a result of the support-cluster interaction.

Hunt, D.J.; Jackson, S.D.; Moyes, R.B.; Wells, P.B.; Whyman, R.

1984-04-01T23:59:59.000Z

124

Studies of the coadsorption of deuterium and carbon monoxide with silver on rhodium and the adsorption of 2,4,6-trinitrotoluene on clean and carbon covered platinum  

SciTech Connect (OSTI)

Ag adsorbed on Rh(100) is presented as a model of the corresponding bimetallic catalyst. Ag overlayer growth follows the Frank-Van der Merwe growth mechanism at 300 K and the Stranski-Krastanov growth mechanism at 640 K. Ag(3d) binding energies are found to track the vacuum level rather than the Fermi level. The results of D/sub 2/ and CO adsorption studies on Ag/Rh(100) show that adsorbed Ag does not significantly alter the properties of adjacent D/sub 2/ or CO adsorption sites on the Rh(100) surface. The desorption and decomposition of 2,4,6-trinitrotoluene (TNT) on clean and carbon covered Pt(111) is also reported. No evidence for TNT decomposition on the carbon covered surface is found. Molecular TNT desorption kinetics at low coverage are first order, yielding an activation energy of 16.7 +/- 1 Kcal/mol and a preexponential factor of 2.3 x 10/sup 11/ (x e/sup - + 0.5/) sec/sup -1/. TNT adsorbed on the clean Pt(111) surface at submonolayer coverages undergoes almost complete decomposition during heating. The major decomposition products are H/sub 2/O, NO, CO/sub 2/, CO, HCN, and a carbon residue left on the surface. TNT adsorbed in the second and higher monolayers desorbs molecularly. The significance of these results in understanding the performance of a commercial explosive vapor preconcentrator is discussed.

Peebles, H.C.

1983-01-01T23:59:59.000Z

125

FTIR study of hydrogen and carbon monoxide adsorption on Pt/TiO{sub 2}, Pt/ZrO{sub 2}, and Pt/Al{sub 2}O{sub 3}  

SciTech Connect (OSTI)

The Pt/TiO{sub 2}, Pt/ZrO{sub 2}, and Pt/Al{sub 2}O{sub 3} catalysts submitted to low-temperature reduction (LTR,200 C) and high-temperature reduction (HTR, 500 C) and exposed to hydrogen and carbon monoxide at room temperature were studied by infrared spectroscopy. There is a strong loss of transmission in the entire infrared spectra on Pt/TiO{sub 2} after its exposure to hydrogen, which is related to the reducibility of the support. A typical SMSI behavior (strong metal-support interaction), such as the decrease in carbon monoxide adsorption capacity, was detected on Pt/TiO{sub 2} and Pt/ZrO{sub 2} after exposure to hydrogen, even for the catalysts submitted to LTR treatment. Also a carbonyl band shift to lower wavenumber was observed on LTR-treated Pt/TiO{sub 2}, Pt/ZrO{sub 2}, and Pt/Al{sub 2}O{sub 3} after exposure to hydrogen. The authors interpreted this SMSI behavior as an electronic rather than morphological effect, which was induced by the presence of hydrogen spillover.

Benvenutti, E.V.; Franken, L.; Moro, C.C.; Davanzo, C.U.

1999-11-09T23:59:59.000Z

126

Visible-Light Photoredox Catalysis: Selective Reduction of Carbon Dioxide to Carbon Monoxide by a Nickel N-Heterocyclic Carbene-Isoquinoline Complex  

SciTech Connect (OSTI)

The solar-driven reduction of carbon dioxide to value-added chemical fuels is a longstanding challenge in the fields of catalysis, energy science, and green chemistry. In order to develop effective CO2 fixation, several key considerations must be balanced, including (1) catalyst selectivity for promoting CO2 reduction over competing hydrogen generation from proton reduction, (2) visible-light harvesting that matches the solar spectrum, and (3) the use of cheap and earth-abundant catalytic components. In this report, we present the synthesis and characterization of a new family of earth-abundant nickel complexes supported by N-heterocyclic carbene amine ligands that exhibit high selectivity and activity for the electrocatalytic and photocatalytic conversion of CO2 to CO. Systematic changes in the carbene and amine donors of the ligand have been surveyed, and [Ni(Prbimiq1)]2+ (1c, where Prbimiq1 = bis(3-(imidazolyl)isoquinolinyl)propane) emerges as a catalyst for electrochemical reduction of CO2 with the lowest cathodic onset potential (Ecat = 1.2 V vs SCE). Using this earth-abundant catalyst with Ir(ppy)3 (where ppy = 2-phenylpyridine) and an electron donor, we have developed a visible-light photoredox system for the catalytic conversion of CO2 to CO that proceeds with high selectivity and activity and achieves turnover numbers and turnover frequencies reaching 98,000 and 3.9 s1, respectively. Further studies reveal that the overall efficiency of this solar-to-fuel cycle may be limited by the formation of the active Ni catalyst and/or the chemical reduction of CO2 to CO at the reduced nickel center and provide a starting point for improved photoredox systems for sustainable carbon-neutral energy conversion.

Thoi, VanSara; Kornienko, Nick; Margarit, C; Yang, Peidong; Chang, Christopher

2013-06-07T23:59:59.000Z

127

The structure of adsorbed sulfur and carbon on molybdenum and rhenium single crystal surfaces, and their influence on carbon monoxide and hydrocarbon chemisorption  

SciTech Connect (OSTI)

An ultra-high vacuum (10/sup -10/ Torr) study was performed on the chemisorption and structures of S and C adsorbates on Mo(100), Re(0001), and Re(1010) single crystal surfaces. Both S and C adsorb strongly on Mo(100), Re(0001), and Re(1010), with adsorption energies >70 kcal/mol for coverages less than saturation. S was proposed to adsorb in the highest symmetry sites on all surfaces except for theta/sub s/ > 0.75 on Mo(100), where studies suggest two different adsorption sites. C adsorbs in a ''carbidic'' or active phase on Mo(100), where it is also proposed to adsorb in the highest symmetry sites. However, C adsorbs in a ''graphitic'' or inactive phase on Re(0001) and Re(1010). CO chemisorption on the S and C overlayers was found to be blocked (except for C on Mo(100)), with S blocking adsorption more efficiently than C. Changes in adsorption energy were determined to be caused by local crowding of CO molecules by S or C, rather than a long-range electronic interaction. Unsaturated hydrocarbons decomposed completely on Mo(100), Re(0001), and Re(1010). Similar to the results for CO chemisorption, strong adsorption of unsaturated hydrocarbons (leading to decomposition) was blocked by pre-adsorbed S, allowing only physisorption to occur (adsorption energies < 11 kcal/mol). The effect of pre-adsorbed ''graphitic'' C on Re(0001) and Re(1010) on unsaturated hydrocarbon chemisorption was the same; strong adsorption (leading to decomposition) was blocked allowing only physisorption. However, Mo(100) with pre-adsorbed ''carbidic'' carbon blocks only decomposition while allowing strong reversible molecular chemisorption (12 to 23 kcal/mol). Differences in inhibition efficiency of S and C are proposed to be caused by differences in bond distances of the adsorbates to the surface. Greater distance from the metal surface causes more interaction with neighboring metal atoms. These differences also suggest explanations for catalytic hydrodesulfurization of thiophene.

Kelly, D.G.

1987-08-01T23:59:59.000Z

128

Synthesis and reactivity of sterically congested metallacyclobutenes and metal-mediated carbon-sulfur bond activation  

E-Print Network [OSTI]

methods for this conversion typically involve the production of byproducts like carbon monoxide and hydrogen

Vélez, Carmen L.

2011-01-01T23:59:59.000Z

129

Exhaust-catalyst development for methanol-fueled vehicles. II. Synergism between palladium and silver in methanol and carbon monoxide oxidation over an alumina-supported palladium-silver catalyst  

SciTech Connect (OSTI)

Methanol and carbon monoxide oxidation were examined over 0.01 Pd, 5% Ag, and 0.01% Pd/5% Ag catalysts - all supported on ..gamma..-alumina. The bimetallic catalyst showed greater CO and CH/sub 3/OH oxidation activity than either of the single-component catalysts; moreover, the Pd and Ag interacted synergistically in the bimetallic catalyst to produce greater CO and CH/sub 3/OH oxidation rates and lower yields of methanol partial oxidation products than expected from a mixture of the single-component catalysts. Temperature-programmed oxidation experiments and reactivity experiments involving changes in O/sub 2/ partial pressure both provided evidence that the Pd-Ag synergism results from Pd promoting the rate of O/sub 2/ adsorption and reaction with CO and CH/sub 3/OH on Ag. The data also indicate that virtually all of the Pd in the bimetallic catalyst is present in Pd-Ag crystallites.

McCabe, R.W.; Mitchell, P.J.

1987-02-01T23:59:59.000Z

130

TableHC10.13.xls  

Gasoline and Diesel Fuel Update (EIA)

or More... 0.3 Q Q Q Q Lighting Usage Indicators U.S. Census Region Northeast Midwest Table HC10.13 Lighting Usage...

131

ZIRCONIA-BASED MIXED POTENTIAL CARBON MONOXIDE/HYDROCARBON SENSORS WITH LANTHANUM MAGNESIUM OXIDE, AND TERBIUM-DOPED YTTRIUM STABILIZED ZIRCONIA ELECTRODES  

SciTech Connect (OSTI)

We have investigated the performance of dual metal oxide electrode mixed potential sensors in an engine-out, dynamometer environment. Sensors were fabricated by sputtering thin films of LaMnO{sub 3} and Tb-doped YSZ onto YSZ electrolyte. Au gauze held onto the metal oxide thin films with Au ink was used for current collection. The exhaust gas from a 4.8L, V8 engine operated in open loop, steady-state mode around stoichiometry at 1500 RPM and 50 Nm. The sensor showed a stable EMF response (with no hysteresis) to varying concentrations of total exhaust gas HC content. The sensor response was measured at 620 and 670 C and shows temperature behavior characteristic of mixed potential-type sensors. The results of these engine-dynamometer tests are encouraging; however, the limitations associated with Au current collection present the biggest impediment to automotive use.

E. L. BROSHA; R. MUKUNDAN; ET AL

2000-10-01T23:59:59.000Z

132

Sulfur tolerant molten carbonate fuel cell anode and process  

DOE Patents [OSTI]

Molten carbonate fuel cell anodes incorporating a sulfur tolerant carbon monoxide to hydrogen water-gas-shift catalyst provide in situ conversion of carbon monoxide to hydrogen for improved fuel cell operation using fuel gas mixtures of over about 10 volume percent carbon monoxide and up to about 10 ppm hydrogen sulfide.

Remick, Robert J. (Naperville, IL)

1990-01-01T23:59:59.000Z

133

A DFT Study of Interaction of Carbon Monoxide with Carbonaceous Materials Juan F. Espinal, Alejandro Montoya, Fanor Mondragon,*, and Thanh N. Truong*,  

E-Print Network [OSTI]

is an important process in the gasification of carbon materials such as char, coke, soot, as well as in the growth it is a clean and efficient alternative to the use of coal instead of combustion. The gasification process

Truong, Thanh N.

134

TableHC11.12.xls  

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

... 2.8 0.3 Q 0.2 Million U.S. Housing Units Home Electronics Usage Indicators Table HC11.12 Home Electronics Usage Indicators by Northeast Census Region,...

135

TableHC6.13.xls  

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

Q 5 or More... 0.3 N Q Q Q Q Lighting Usage Indicators 4 Members 5 or More Members Table HC6.13 Lighting Usage Indicators by...

136

Use of carbon monoxide and third-derivative EPR spectra to probe the coordination of surface V/sup 4 +/ ions on reduced V/sub 2/O/sub 5//SiO/sub 2/ catalysts  

SciTech Connect (OSTI)

The coordination properties of surface V/sup 4 +/ ions of reduced V/sub 2/O/sub 5/ supported on silica have been studied by EPR using the adsorption of various probe molecules. The spectrum resolution, greatly enhanced with the third-derivative presentation, indicates an orthorhombic symmetry for the V/sup 4 +/ ions after CO adsorption (g/sub 1/ approx. g/sub 2/ = 1.985, g/sub 3/ = 1.931, A/sub 1/ approx. A/sub 2/ 71.4 G, A/sub 3/ = 191.4 G). The use of /sup 13/C-enriched carbon monoxide allows us to observe that the V/sup 4 +/ surface ions can coordinate two CO molecules from the gas phase to form, together with four lattice oxide ions, a distorted octahedron with one pronounced vanadyl character bond. The /sup 13/C superhyperfine coupling constant is found to be about 7 G. The influence of the adsorbed molecules (CO, H/sub 2/O, C/sub 2/H/sub 4/) on the properties of the V/sup 4 +/ ions at the surface is further discussed. 33 references, 4 figures, 1 table.

Che, M.; Canosa, B.; Gonzalez-Elipe, A.R.

1986-02-13T23:59:59.000Z

137

Interaction of carbon monoxide with oxygen in the adsorbed layer on Pd, Ce, Pd-Ce catalysts supported on /gamma/-Al/sub 2/O/sub 3/  

SciTech Connect (OSTI)

The adsorption of CO and the interaction of CO/sub ads/ with O/sub 2/ on Pd, Ce, and Pd-Ce//gamma/-Al/sub 2/O/sub 3/ (0.5 wt. % Pd, 2.0 wt. % Ce) has been studied using the methods of IR spectroscopy and differential scanning calorimetry. The identity of the adsorbed CO complexes, the temperature ranges over which they desorb, and their reactivity with O/sub 2/ have been established. The interaction of bridging and carbonate - carboxylate CO complexes and carbon (disproportionation and dissociation products) with O/sub 2/ on Pd and Pd-Ce catalysts is preceded by the coadsorption of oxygen and the evolution of heat. During the oxidation of CO, autooscillation, heat evolution, and the concentration of oxygen in the flow are observed.

Savel'eva, G.A.; Sass, A.S.; Speranskaya, G.V.; Tenchev, K.K.; Petrov, L.A.; Vozdvizhenskii, V.F.; Galeev, T.K.; Popova, N.M.

1989-01-01T23:59:59.000Z

138

Conversion of carbon monoxide on membrane catalysts of palladium alloys. I. Reaction between CO and H/sub 2/ on binary palladium alloys with ruthenium and nickel  

SciTech Connect (OSTI)

The formation of saturated and unsaturated C/sub 1/ and C/sub 2/ hydrocarbons, carbon dioxide and water is observed during reaction CO and H/sub 2/ on binary palladium alloys with 10 wt. % of Ru and 5.5 wt. % Ni at atmospheric pressure and 523-683 K. The introduction of hydrogen into the reaction zone by different methods, bu diffusion through a membrane catalyst or in a mixture with CO, influences the activity and selectivity of the catalysts investigated.

Gur'yanova, O.S.; Serov, Yu.M.; Gyl'yanova, S.G.; Gryaznov, V.M.

1989-01-01T23:59:59.000Z

139

Office of HC Policy, Accountability, and Technology (HC-10) | Department of  

Broader source: Energy.gov (indexed) [DOE]

Policy, Accountability, Policy, Accountability, and Technology (HC-10) Office of HC Policy, Accountability, and Technology (HC-10) Mission and Function Statement This organization supports the program objectives and missions of all Departmental components by (1) developing Department-level human capital management (HCM) and training/development policies, (2) developing human capital management strategies that provide the direction and structure for Departmental HCM programs, (3) developing HCM legislative proposals; (4) supplying HCM policy advice and guidance within the Department; and (5) developing and implementing innovative HCM business solutions relating to corporate recruiting, talent capacity, diversity outreach, and technology innovations. Strategic directions are influenced by an analysis of budget and workforce

140

Office of HC Strategy Budget and Performance Metrics (HC-50) | Department  

Broader source: Energy.gov (indexed) [DOE]

Strategy Budget and Strategy Budget and Performance Metrics (HC-50) Office of HC Strategy Budget and Performance Metrics (HC-50) Mission Statement and Function Statement The Office of Human Capital Strategy, Budget, and Performance Metrics provides strategic direction and advice to its stakeholders through the integration of budget analysis, workforce projections, and performance metrics in support of the goals and missions of the Department of Energy. Functions: Promotes business partnerships with Departmental elements to define and design HCM implementation strategies in alignment with Departmental mission, goals, and objectives. Provides strategic direction and advice through analysis of budget, workforce projections, and performance to respond to congressional mandates, administration goals, Departmental priorities and mission needs.

Note: This page contains sample records for the topic "hc carbon monoxide" 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

Identifying and counting point defects in carbon nanotubes  

E-Print Network [OSTI]

of single-walled carbon nanotubes. J. Phys. Chem. B 103,single-walled carbon nanotubes on patterned silicon wafers.of single-walled carbon nanotubes from carbon monoxide.

Fan, Y W; Goldsmith, B R; Collins, Philip G

2005-01-01T23:59:59.000Z

142

Identifying and Counting Point Defects in Carbon Nanotubes  

E-Print Network [OSTI]

single-walled carbon nanotubes on patterned silicon wafers.of single-walled carbon nanotubes from carbon monoxide.single-walled carbon nanotubes. Science 306, 1362–1364 (

Collins, Philip G

2005-01-01T23:59:59.000Z

143

Performance Metrics and Budget Division (HC-51) | Department of Energy  

Broader source: Energy.gov (indexed) [DOE]

Performance Metrics and Budget Division (HC-51) Performance Metrics and Budget Division (HC-51) Performance Metrics and Budget Division (HC-51) MISSION: The mission of the Performance Metrics and Budget Division (HC-51) is to support the effective and efficient implementation of the Department of Energy's human capital initiatives and functions through the strategic integration of corporate human capital performance metrics and the budget of the Office of the Chief Human Capital Officer (HC). FUNCTIONS: Human capital performance measurement and strategic functions at the DOE and interagency levels include: Provides analytical support and strategic advice to internal and external HC stakeholders on the appropriate and effective use of performance metrics as a key to effective strategic human capital management.

144

DOE Learning & Development Competency Governance Structure Senior HC Leadership  

Broader source: Energy.gov (indexed) [DOE]

Learning & Development Learning & Development Competency Governance Structure Senior HC Leadership HC DOE L&D BOD HC-20 Other HR Functions (e.g. Staffing) (Competency Steward) Competency Management HC-23 Other DOE Working and Users Groups Lead Competency Stakeholders (CMWG and CMUG) Management Program (e.g. Union Reps, (CMP) to ensure validity and career & professional consistency of competencies development programs Lead Implementation and Operation of automated Competency Management System (CMS) Competency Steward -Supplies HR/Competency Development subject matter expertise -Maintains DOE Competency Framework and Competency Dictionary to ensure common, valid approaches are used to develop and

145

The Impact of PM and HC on EGR Cooler Fouling  

Broader source: Energy.gov [DOE]

Data were used to correlate an EGR cooling fouling model developed to test the impact of PM and HC on fouling

146

Investigations on emission characteristics of the pongamia biodiesel–diesel blend fuelled twin cylinder compression ignition direct injection engine using exhaust gas recirculation methodology and dimethyl carbonate as additive  

Science Journals Connector (OSTI)

Experiments were carried out on a twin cylinder direct injection compression ignition engine using pongamia biodiesel–diesel blend as fuel with exhaust gas recirculation (EGR) and dimethyl carbonate (DMC) as additive. The experimental results showed that pongamia biodiesel–diesel blend fuelled engine with EGR and DMC can simultaneously reduce smoke and nitric oxide ( NO x ) emission. The NO x emission was reduced by about 17.68% for 10% of EGR introduction and about 13.55% increase in smoke emission. When dimethyl carbonate was added with EGR the engine emits lower smoke with lesser NO x emission and it showed that the smoke reduction rate had a linear relationship with DMC percentage. The carbon monoxide (CO) and hydrocarbon (HC) emissions also decreased when DMC was added. However the addition of DMC with EGR caused an increase in both BSEC and BTE.

M. Pandian; S. P. Sivapirakasam; M. Udayakumar

2010-01-01T23:59:59.000Z

147

Flame/Wall interactions : laminar study of unburnt HC formation  

E-Print Network [OSTI]

for an important part to the sources of hydrocarbon (HC) emission in a combustion chamber. The aim of this work in gasoline engine. A skeletal mechanism (29 species and 48 reactions) mimicking iso-octane combustion is used, wall heat flux, quench distances as well as HC families are investigated by varying parameters like

Paris-Sud XI, Université de

148

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

149

Information Management Division (HC-14) | Department of Energy  

Broader source: Energy.gov (indexed) [DOE]

Information Management Division (HC-14) Information Management Division (HC-14) Information Management Division (HC-14) Mission Statement This division provides operational support and consultative advice to the Chief Human Capital Officer and Departmental Senior Management on matters pertaining to the acquisition, deployment and maintenance of enabling technology to support the tactical and strategic management of human capital related to accomplishing Department goals and program objectives. The mission also entails establishing and providing assistance and guidance on the use of technology-supported business process reengineering; investment analysis; performance measurement; strategic development and application of information systems and infrastructure; policies to provide improved management of information resources and technology; and better,

150

Employment Solutions Division (HC-13) | Department of Energy  

Broader source: Energy.gov (indexed) [DOE]

Employment Solutions Division (HC-13) Employment Solutions Division (HC-13) Employment Solutions Division (HC-13) Mission Statement This division develops and implements innovative HCM business solutions relating to corporate recruiting, organizational and workforce development, workforce and succession planning, talent capacity, and diversity outreach. Functions Directing the activities of the Corporate Outreach and Recruitment Council (with representatives from across the Department including NNSA, the Power Marketing Administrations, and the National Labs); including enhancing entry-level and mid to senior level hiring across DOE, furthering the use of automated technology in outreach and recruitment efforts, designing effective marketing and branding efforts to attract the right candidate for the right job, incorporating diversity strategies, and

151

HQ Operations Division (HC-32) | Department of Energy  

Broader source: Energy.gov (indexed) [DOE]

Operations Division (HC-32) Operations Division (HC-32) HQ Operations Division (HC-32) Functions Deliver employment operational and advisory services, including position management, recruitment, staffing and classification, reduction in force in Headquarters; Provide operational and advisory support for competitive sourcing initiatives and impacted serviced population; Provide information to HQ employee population on employee benefit programs (retirement; health, dental, vision, long-term care, and life insurance; thrift savings plan; flexible spending accounts; the transit subsidy program; and annual and sick leave, and long-term care through individual consultation, new employee orientation and exit interviews; Deliver a range of human resources personnel processing functions to employees in HQ organizations, including processing actions, OPF

152

Workforce Analysis and Planning Division (HC-52) | Department of Energy  

Broader source: Energy.gov (indexed) [DOE]

Workforce Analysis and Planning Division (HC-52) Workforce Analysis and Planning Division (HC-52) Workforce Analysis and Planning Division (HC-52) Mission Statement: This division provides strategic direction guidance and advice through analysis of budget and workforce projections and plans, congressional mandates, administration goals, Departmental priorities and mission needs. FUNCTIONS: Develops business intelligence, demographic and trend analyses in support of corporate workforce planning and in response to requests from within the Department and from external oversight agencies. Analyzes and evaluates workforce plans, employment trends, budget development and implementation, Departmental studies and human capital assessment systems. Develops staffing targets and tracks staffing management throughout the Department to identify needs for new or changing

153

Human Capital Policy Division (HC-11) | Department of Energy  

Broader source: Energy.gov (indexed) [DOE]

About Us » Organization » Policy, Accountability, and Technology About Us » Organization » Policy, Accountability, and Technology (HC-10) » Human Capital Policy Division (HC-11) Human Capital Policy Division (HC-11) Mission Statement This division serves as the HCM policy arm for the Department. It supports program objectives and missions of all DOE components by developing HCM-related policies and strategies and supplies advice and guidance across the Department. Functions Provide a full range of staff support to the Chief Human Capital Officer including support required for internal and external responsibilities. Develop and revise the agency human capital management strategy in support of the overall departmental strategic plan. Seek out, influence and translate legislative and regulatory direction into Departmental strategies, policies and programs to address

154

HC Policy and Services - Points of Contact | Department of Energy  

Broader source: Energy.gov (indexed) [DOE]

HC Policy and Services - Points of Contact HC Policy and Services - Points of Contact HC Policy and Services - Points of Contact Learning and Development Contact Email Phone Executive Learning Rosenmarkle, David P david.rosenmarkle@hq.doe.gov 202-586-7978 Technical and Professional Skills Dent, Cheri D cheri.dent@hq.doe.gov 202-586-9556 Supervisory Training Robinson, June V june.robinson@hq.doe.gov 202-586-9557 Competency Development Coleman, Eric eric.coleman@hq.doe.gov 202-586-8466 Organizational Development Coleman, Eric eric.coleman@hq.doe.gov 202-586-8466 Skills Assessment Coleman, Eric eric.coleman@hq.doe.gov 202-586-8466 Mission Critical Occupations Coleman, Eric eric.coleman@hq.doe.gov 202-586-8466 Training and Program Evaluation Welcome, Deadra deadra.welcome@hq.doe.gov 202-586-9533

155

Office of Executive Resources (HC-40) | Department of Energy  

Broader source: Energy.gov (indexed) [DOE]

Executive Resources (HC-40) Executive Resources (HC-40) Office of Executive Resources (HC-40) Mission and Function Statement This organization provides a full range of human capital management workforce services and support as well as policy guidance functions to senior level positions (SES, SL, and ST), excepted service positions (EJ, EK, and ARPA-E ET/ER) and political appointments for the Department. This includes: Providing operational and advisory executive services to Headquarters and field components, including political appointees and the immediate Office of the Secretary. Providing operational support to the Department's Executive Resources and Performance Review Boards. Administering the SES and SL/ST performance management systems and recognition and awards programs. Managing the SES Candidate Development Program.

156

E-Print Network 3.0 - americium carbonates Sample Search Results  

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

air pollutants are defined in the Clean Air Act and include ozone, particulate matter, carbon monoxide... .g., americium-241, cesium- 137, plutonium-238, plutonium-239, uranium-...

157

Hackathon Project (HC-04): Ontology Summit 2013 Content Hack  

E-Print Network [OSTI]

developed by Northeastern University and CIM3. #12;Ontology Summit 2013 Content Hack 6 Ontology Summit 2013Hackathon Project (HC-04): Ontology Summit 2013 Content Hack Leveraging Semantics on OntologPSMW Ken Baclawski Marcela Vegetti (co-champions) #12;Ontology Summit 2013 Content Hack 2 Background

Baclawski, Kenneth B.

158

Project and Survey Staff (HC-50.1) | Department of Energy  

Broader source: Energy.gov (indexed) [DOE]

Project and Survey Staff (HC-50.1) Project and Survey Staff (HC-50.1) Project and Survey Staff (HC-50.1) Functional Statement The Project and Survey Staff (HC-50.1) report to the Office of Human Capital Strategy, Budget, and Performance Metrics (HC-50). The Project and Survey Staff work with other HC-50 divisions to provide strategic direction and advice to stakeholders through budget analysis, workforce projections, and performance metrics. HC-50.1 facilitates the integration of HR program functions and cultivates business partnerships with Program and Staff Offices (PSO) within the Department to define and design Human Capital Management (HCM) implementation strategies for establishing and sustaining consistent quality management functions throughout Human Capital (HC). These partnerships serve to ensure that human capital management

159

Ag-Al2O3 Catalyst HC-SCR: Performance with Light Alcohols and...  

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

Ag-Al2O3 Catalyst HC-SCR: Performance with Light Alcohols and Other Reductants Ag-Al2O3 Catalyst HC-SCR: Performance with Light Alcohols and Other Reductants 2004 Diesel Engine...

160

Engine and Reactor Evaluations of HC-SCR for Diesel NOx Reduction...  

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

Engine and Reactor Evaluations of HC-SCR for Diesel NOx Reduction Engine and Reactor Evaluations of HC-SCR for Diesel NOx Reduction Focus is the heavy duty, US dynamometer...

Note: This page contains sample records for the topic "hc carbon monoxide" 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

A New Approach to Carbon Gasification  

Science Journals Connector (OSTI)

... carbon monoxide plus hydrogen respectively, under the usual conditions of temperature and pressure applying in gasification practice, the rates of reaction measured by the number of gm. moles of product ...

J. D. BLACKWOOD; F. K. McTAGGART

1959-08-08T23:59:59.000Z

162

Plasmachemical Synthesis of Carbon Suboxide  

E-Print Network [OSTI]

A nonthermal carbon monoxide plasma is known to produce a solid deposition which is thought to be a polymer of carbon suboxide (C3O2); however there are very few investigations of this deposition in the literature. This thesis contains an analysis...

Geiger, Robert

2012-12-11T23:59:59.000Z

163

Office of the Chief Human Capital Officer (HC-1) | Department of Energy  

Broader source: Energy.gov (indexed) [DOE]

the Chief Human Capital the Chief Human Capital Officer (HC-1) Office of the Chief Human Capital Officer (HC-1) HC-1 Mission and Function Statement The Office of the Chief Human Capital Officer (HC) provides leadership to the Department of Energy (DOE) on the impact and use of policies, proposals, programs, and partnership agreements/relationships related to all aspects of Human Capital Management (HCM). Within the framework of the organization, HCM is an integrated approach that links human resources, training/development and diversity. HC develops, deploys and assesses a full range of short and long term human capital management solutions, policies and programs and proactively seeks additional solutions and approaches to serve the needs of the Department. HC advances and supports

164

Hydrocarbon Inhibition and HC Storage Modeling in Fe-Zeolite Catalysts for HD Diesel Engines  

Broader source: Energy.gov [DOE]

Investigating the dynamics between various aftertreatment devices for overall optimal performance to simultaneously reduce NOx and PM. Ex: HC poisoning/inhibition on zeolites1, catalyst aging, etc.

165

Detection of Carbon Monoxide within the Magellanic Bridge  

E-Print Network [OSTI]

The Mopra 22m and SEST 15m telescopes have been used to detect and partially map a region of 12CO(1-0) line emission within the Magellanic Bridge, a region lying between the Large and Small Magellanic Clouds. The emission appears to be embedded in a cloud of neutral hydrogen, and is in the vicinity of an IRAS source. The CO emission region is found to have a 60um/100um flux density ratio typical for 12CO(1-0) detections within the SMC, although it has a significantly lower 12CO brightness and velocity width. These suggest that the observed region is of a low metallicity, supporting earlier findings that the Magellanic Bridge is not as evolved as the SMC and Magellanic Stream, which are themselves of a lower metallicity than the Galaxy. Our observations, along with empirical models based on SMC observations, indicate that the radius of the detected CO region has an upper limit of ~16 pc. This detection is, to our knowledge, the first detection of CO emission from the Magellanic Bridge and is the only direct evidence of star formation through molecular cloud collapse in this region.

E. Muller; L. Staveley-Smith; W. Zealey

2002-09-25T23:59:59.000Z

166

Studies of carbon monoxide diffusion in an urban area  

E-Print Network [OSTI]

3 40 ( )-, 7) 50 I I ) 'I ' 0 (. ' i . l') 4! !, , /' / 600 700 TRAFFTC/15 N!. Ii Fig. 14. Carl~co moaoxicle come. atrat ion v, traffic for Sampler 2 fro' t 12 15PN7 00PYCI/To ? 'JU)v 20' 1969(r'057) 29 if] 8!. & vcti jr. ';"; /I 7... correlation co"fficient 0. 47% 16. 6% 2. 44% 0. 13% Table 10 sboms 95/ confislence limits for average values for the three days. T1-e...

Thomas, John Charles

2012-06-07T23:59:59.000Z

167

Oxidation of Carbon Monoxide in Cell Extracts of Pseudomonas carboxydovorans  

Science Journals Connector (OSTI)

...Winzer. 1932. Uber die Bildung von Essigsaure bei der biologischen Umsetzung von Kohlenoxyd und Kohlensaure mit Wasserstoff zu Methan. Biochem. Z. 245:2-12. 9. Fuchs, G., G. Andress, and R. K. Thauer. 1975. CO- oxidation by anaerobic...

Ortwin Meyer; Hans G. Schlegel

1979-02-01T23:59:59.000Z

168

Advanced Diesel Combustion with Low Hydrocarbon and Carbon Monoxide Emissions  

Broader source: Energy.gov [DOE]

Poster presented at the 16th Directions in Engine-Efficiency and Emissions Research (DEER) Conference in Detroit, MI, September 27-30, 2010.

169

ILENR/RE-AQ-ON-ROAD CARBON MONOXIDE AND HYDROCARBON  

E-Print Network [OSTI]

. McVey, and Stuart P. Beaton Prepared for: Illinois Department of Energy and Natural Resources Office A. Witter Director State of Illinois Illinois Department of Energy and Natural Resources #12;NOTE This report has been reviewed by the Illinois Department of Energy and Natural Resources (ENR) and approved

Denver, University of

170

Computer simulation of the dispersion of carbon monoxide from roadways  

E-Print Network [OSTI]

and that the transport of material in the x-direction is due mainly to the mean wind, one can reduce equation (1) to BB B BV B BB u ? = ? (K ? ) + ? (K ? ) Bx By y By Bz z Bz (4) with the following boundary conditions, 1) I ~ 0 as x -+ 2) V~ asx-+0 (5) 3... are illustrated in Figures 5 and 6. Using equations (24) and (25) with n = 1 and equation (21), the concentration equations (19) and (20) become Q 1 v 21 r&(x, y, z, h) 2rra a u exp P- ? (~) J L2 ~ z z-h) 1 z+h)2 a az 'z (28) t(x, z, h) = exp /2rr a u z...

Maldonado, Cesar

1976-01-01T23:59:59.000Z

171

Decomposition and Polymerization of Solid Carbon Monoxide under Pressure  

Science Journals Connector (OSTI)

By performing constant-pressure deformable-cell ab initio molecular dynamics simulations we have studied the pressure-induced chemical instability of CO above 5 GPa. The simulation shows that, contrary to previous speculations, polymerization proceeds without CO bond dissociation. The resulting polymer consists of a disordered network of small polycarbonyl (CO)n chains connecting fivefold C4O cycles. The computed vibrational spectra and electronic gap agree very well with (and shed light on) very recent experimental data.

Stéphane Bernard; Guido L. Chiarotti; Sandro Scandolo; Erio Tosatti

1998-09-07T23:59:59.000Z

172

Metal catalyzed copolymerization processes involving carbon oxides as substrates  

E-Print Network [OSTI]

backbone and electron donating tert-butyl groups in the phenolate rings. This catalyst was used to investigate the effect of altering the nature of the cocatalyst and its concentration. The coupling of carbon monoxide and aziridines has been shown...

Phelps, Andrea Lee

2005-11-01T23:59:59.000Z

173

Population based exposure assessment methodology for carbon monoxide: Development of a Carbon Monoxide Passive Sampler and Occupational Dosimeter  

E-Print Network [OSTI]

monitoring for nitrogen dioxide exposure: methodologyB.G. , Jr. (1983) Nitrogen dioxide inside and outside 137Personal Sampler for Nitrogen Dioxide. American Industrial

Apte, Michael G.

2010-01-01T23:59:59.000Z

174

Carbon dioxide recovery from an integrated coal gasifier, combined cycle plant using membrane separation and a CO2 gas turbine  

Science Journals Connector (OSTI)

A scheme is described for electricity production based on coal gasification with recovery of carbon dioxide. In this scheme, coal is gasified into a coal gas, consisting mainly of hydrogen and carbon monoxide. A ...

Chris Hendriks

1994-01-01T23:59:59.000Z

175

FEAT Equations for CO, HC and NO. G. A. Bishop Last updated June 2011. ASSUMPTIONS  

E-Print Network [OSTI]

:H ratio is 2 and non-oxygenated. Applies to gasoline and diesel in general. Fuel is approximated make the math simpler we have chosen for the exhaust HC to be a multiple of the input HC are correct for diesel vehicles) and assume an 8cm path length. For a direct tailpipe comparison for diesel

Denver, University of

176

University of California, Santa Cruz Student Health Services HC: 1017 (11/20/13) Meningitis Handout  

E-Print Network [OSTI]

be treated? Only people who have been in close contact (household members, intimate contacts, health careUniversity of California, Santa Cruz Student Health Services HC: 1017 (11/20/13) Meningitis Handout-459-2591. #12;University of California, Santa Cruz Student Health Services HC: 1017 (11/20/13) Meningitis

California at Santa Cruz, University of

177

Evaluation of HC1 measurement techniques at municipal and hazardous-waste incinerators  

SciTech Connect (OSTI)

Hydrogen chloride (HC1) emissions from hazardous waste incinerators are regulated by the EPA, and the Agency is considering HC1 regulations for municipal waste combustors. Until recently, techniques to adequately quantify these emissions using either instrumentation or wet-chemistry sampling methods have not been evaluated. The EPA has sponsored several field tests to assess the performance of commercially-available HC1 continuous emission monitoring systems (CEMS's) and a proposed manual sampling and analysis methodology for use at municipal and hazardous waste incinerators. Tests were performed (1) to determine the capability of HC1 CEMS's to provide valid measurement data, (2) to develop HC1 CEMS performance specifications, and (3) to develop a suitable performance test method.

Shanklin, S.A.; Steinsberger, S.C.; Logan, T.J.; Rollins, R.

1990-01-01T23:59:59.000Z

178

file://C:\Documents%20and%20Settings\VM3\My%20Documents\hc6-1a_  

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

Table HC6-1a. Usage Indicators by Climate Zone, Table HC6-1a. Usage Indicators by Climate Zone, Million U.S. Households, 2001 ________________________________________________________________________________________________________ | | | | | Climate Zone 1 | | |_________________________________________________| | | | | | | Fewer than 2,000 CDD and -- | |

179

HC-Pro Suppression of Transgene Silencing Eliminates the Small RNAs but Not Transgene Methylation or the Mobile Signal  

Science Journals Connector (OSTI)

...and if HC-Pro interferes with this process, we developed a polymerase chain reaction...enzyme ( ), HC-Pro may target the process at this step. There are several possible...the two branches of gene silencing are interrelated and if HC-Pro affects VIGS in the same...

Allison C. Mallory; Lara Ely; Trent H. Smith; Rajendra Marathe; Radhamani Anandalakshmi; Mathilde Fagard; Herve Vaucheret; Gail Pruss; Lewis Bowman; Vicki B. Vance

180

Observation of the h_c(1P) using e^+e^- collisions above DDbar threshold  

E-Print Network [OSTI]

Using 586pb^-1 of e^+e^- collision data at E_CM = 4170MeV, produced at the CESR collider and collected with the CLEO-c detector, we observe the process e^+e^- --> pi^+ pi^- h_c(1P). We measure its cross section to be 15.6+-2.3+-1.9+-3.0pb, where the third error is due to the external uncertainty on the branching fraction of psi(2S) --> pi^0 h_c(1P), which we use for normalization. We also find evidence for e^+e^- --> eta h_c(1P) at 4170MeV at the 3sigma level, and see hints of a rise in the e^+e^- --> pi^+ pi^- h_c(1P) cross section at 4260MeV.

CLEO Collaboration; T. K. Pedlar; D. Cronin-Hennessy; J. Hietala; S. Dobbs; Z. Metreveli; K. K. Seth; A. Tomaradze; T. Xiao; L. Martin; A. Powell; G. Wilkinson; H. Mendez; J. Y. Ge; D. H. Miller; I. P. J. Shipsey; B. Xin; G. S. Adams; D. Hu; B. Moziak; J. Napolitano; K. M. Ecklund; J. Insler; H. Muramatsu; C. S. Park; L. J. Pearson; E. H. Thorndike; S. Ricciardi; C. Thomas; M. Artuso; S. Blusk; R. Mountain; T. Skwarnicki; S. Stone; L. M. Zhang; G. Bonvicini; D. Cinabro; A. Lincoln; M. J. Smith; P. Zhou; J. Zhu; P. Naik; J. Rademacker; D. M. Asner; K. W. Edwards; K. Randrianarivony; G. Tatishvili; R. A. Briere; H. Vogel; P. U. E. Onyisi; J. L. Rosner; J. P. Alexander; D. G. Cassel; S. Das; R. Ehrlich; L. Gibbons; S. W. Gray; D. L. Hartill; B. K. Heltsley; D. L. Kreinick; V. E. Kuznetsov; J. R. Patterson; D. Peterson; D. Riley; A. Ryd; A. J. Sadoff; X. Shi; W. M. Sun; J. Yelton; P. Rubin; N. Lowrey; S. Mehrabyan; M. Selen; J. Wiss; J. Libby; M. Kornicer; R. E. Mitchell; M. R. Shepherd; C. M. Tarbert; D. Besson

2011-04-11T23:59:59.000Z

Note: This page contains sample records for the topic "hc carbon monoxide" 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

CUT FLOWER VARIETY TRIAL RESULTS 2007 H.C. WIEN, Department of Horticulture  

E-Print Network [OSTI]

1 CUT FLOWER VARIETY TRIAL RESULTS 2007 H.C. WIEN, Department of Horticulture Cornell University series make a single flower look double; Wonderous Light Brown is an attractive caramel color. Pumpkin

Pawlowski, Wojtek

182

Strain-induced band-gap engineering of graphene monoxide and its effect on graphene  

Science Journals Connector (OSTI)

Using first-principles calculations we demonstrate the feasibility of band-gap engineering in two-dimensional crystalline graphene monoxide (GMO), a recently reported graphene-based material with a 1:1 carbon/oxygen ratio. The band gap of GMO, which can be switched between direct and indirect, is tunable over a large range (0–1.35 eV) for accessible strains. Electron and hole transport occurs predominantly along the zigzag and armchair directions (armchair for both) when GMO is a direct- (indirect-) gap semiconductor. A band gap of ?0.5 eV is also induced in graphene at the K? points for GMO/graphene hybrid systems.

H. H. Pu; S. H. Rhim; C. J. Hirschmugl; M. Gajdardziska-Josifovska; M. Weinert; J. H. Chen

2013-02-13T23:59:59.000Z

183

Detection of iodine monoxide in the tropical free troposphere  

E-Print Network [OSTI]

19, 2012) Atmospheric iodine monoxide (IO) is a radical that catalytically destroys heat trapping in the remote tropical marine boundary layer (MBL) (2­4). IO further affects the oxidative capacity iodine species over the remote ocean remain poorly understood (11, 14) but are currently thought

184

Cobalt carbonyl catalyzed olefin hydroformylation in supercritical carbon dioxide  

DOE Patents [OSTI]

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

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

1993-03-30T23:59:59.000Z

185

Zhai, H., H.C. Frey, N.M. Rouphail, G.A. Gonalves, and T.L. Farias, "Fuel Consumption and Emissions Comparisons between Ethanol 85 and Gasoline Fuels for Flexible Fuel Vehicles," Paper No. 2007-AWMA-444, Proceedings, 100th  

E-Print Network [OSTI]

the Alternative Fuel Data Center (AFDC) of the U.S. Department of Energy.4 Carbon dioxide (CO2), CO, and nitricZhai, H., H.C. Frey, N.M. Rouphail, G.A. Gonçalves, and T.L. Farias, "Fuel Consumption and Emissions Comparisons between Ethanol 85 and Gasoline Fuels for Flexible Fuel Vehicles," Paper No. 2007-AWMA

Frey, H. Christopher

186

Snowmobile Contributions to Mobile Source Emissions in Yellowstone  

E-Print Network [OSTI]

measurements of carbon monoxide (CO) and hydrocarbon (HC) emissions were collected from in-use snowmobiles% of the annual emissions of carbon monoxide and 77% of annual emissions of hydrocarbons using an equivalent bestSnowmobile Contributions to Mobile Source Emissions in Yellowstone National Park G A R Y A . B I

Denver, University of

187

Khi i hc k thut thng tin (Undergraduateds School of IES) http://www.uec.ac.jp/ies/faculty/index.html (Jpns)  

E-Print Network [OSTI]

lng Lng t hc Vt liu hc Cht bán dn - Siêu bán dn Thit b in t - Thit b quang in t - T - Vt liu quang Thông tin quang Vt lý rn Sinh hc - Thn kinh hc H thng sinh hc o lng sinh hc Tên thng qun lý doanh nghip... nh hng ngh nghip: K s h thng, K s qun lý sn xut - cht lng sn phm, Chuyên

Yanai, Keiji

188

Carbon dioxide capture process with regenerable sorbents  

DOE Patents [OSTI]

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

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

2002-05-14T23:59:59.000Z

189

Sample collection for high throughput radiation biodosimetry , H.C. Turner1  

E-Print Network [OSTI]

fingerstick-derived blood samples, either to estimate past radiation dose, or to sort individuals exposed, there will be a major need to assess, within a few days, the radiation doses received by tens or hundreds of thousandsSample collection for high throughput radiation biodosimetry G. Garty1 , H.C. Turner1 , Y. Chen2

Simaan, Nabil

190

GeoTran-HC: Geometric transformation of highly coupled variable topology multi-body problems  

Science Journals Connector (OSTI)

Manipulating geometry to prepare a CAD design model for mesh generation is an important step in the finite element analysis (FEA) process. However, complex problems such as electronic chip packages often consist of hundreds or even thousands of sub-features ... Keywords: Cell decomposition, Chip package, FEA modeling, GeoTran-HC, Geometrical transformation, Knowledge-based design and analysis

Sai Zeng; Angran Xiao; Russell S. Peak

2007-09-01T23:59:59.000Z

191

The ebullition of hydrogen, carbon monoxide, methane, carbon dioxide and total gaseous mercury  

E-Print Network [OSTI]

of gaseous species depends of their solubility in the water. Since CH4 is relatively insoluble, ebullition-product of the respiration and is highly soluble in the water, leading ofte h- 1 . Measurements of H2, CO, CH4 and CO2 trapped gas concentrations and fluxes were used

O'Driscoll, Nelson

192

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

E-Print Network [OSTI]

are on the decline of the peak oil production curve, and thedue to the impending peak in oil production and the threatoil production curves for those countries that have passed peak

Smieja, Jonathan Mark

2012-01-01T23:59:59.000Z

193

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

E-Print Network [OSTI]

graph displays not only the shift in energy from wood to fossil fuels but also shows that total energy usagegraph displays not only the shift in energy from wood to fossil fuels, but also shows that total energy usage

Smieja, Jonathan Mark

2012-01-01T23:59:59.000Z

194

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

E-Print Network [OSTI]

compressed air and hydrogen production are all frequently discussed as viable options for future energy storage.

Smieja, Jonathan Mark

2012-01-01T23:59:59.000Z

195

Carbon monoxide and carbon dioxide concentrations in Santiago de Chile associated with traffic emissions  

Science Journals Connector (OSTI)

CO/CO2 ratios have been measured in different locations of Santiago de Chile city. Measurements were carried out in a tunnel (prevailing emissions from cars with catalytic converter) and close to heavy traffic st...

María A. Rubio; Irene Fuenzalida…

2010-03-01T23:59:59.000Z

196

Short-term effects of air pollution: a panel study of blood markers in patients with chronic pulmonary disease  

E-Print Network [OSTI]

monoxide [NO], nitrogen dioxide [NO 2 ], carbon monoxide [monoxide (NO), nitrogen dioxide (NO 2 ), carbon monoxide (dioxide; NO 2 , nitrogen dioxide; CO, carbon monoxide; NO,

2009-01-01T23:59:59.000Z

197

A New Solar Carbon Capture Process: Solar Thermal Electrochemical Photo (STEP) Carbon Capture  

Science Journals Connector (OSTI)

A New Solar Carbon Capture Process: Solar Thermal Electrochemical Photo (STEP) Carbon Capture ... CO2 can be captured from 34% to over 50% solar energy efficiency (depending on the level of solar heat inclusion), as solid carbon and stored, or used as carbon monoxide to be available for a feedstock to synthesize (with STEP generated hydrogen) solar diesel fuel, synthetic jet fuel, or chemical production. ... STEP Iron, a Chemistry of Iron Formation without CO2 Emission: Molten Carbonate Solubility and Electrochemistry of Iron Ore Impurities ...

Stuart Licht; Baohui Wang; Susanta Ghosh; Hina Ayub; Dianlu Jiang; Jason Ganley

2010-07-14T23:59:59.000Z

198

Carbon capture by sorption-enhanced water-gas shift reaction process using hydrotalcite-based material  

SciTech Connect (OSTI)

A novel route for precombustion decarbonization is the sorption-enhanced water-gas shift (SEWGS) process. In this process carbon dioxide is removed from a synthesis gas at elevated temperature by adsorption. Simultaneously, carbon monoxide is converted to carbon dioxide by the water-gas shift reaction. The periodic adsorption and desorption of carbon dioxide is induced by a pressure swing cycle, and the cyclic capacity can be amplified by purging with steam. From previous studies is it known that for SEWGS applications, hydrotalcite-based materials are particularly attractive as sorbent, and commercial high-temperature shift catalysts can be used for the conversion of carbon monoxide. Tablets of a potassium promoted hydrotalcite-based material are characterized in both breakthrough and cyclic experiments in a 2 m tall fixed-bed reactor. When exposed to a mixture of carbon dioxide, steam, and nitrogen at 400{sup o}C, the material shows a breakthrough capacity of 1.4 mmol/g. In subsequent experiments the material was mixed with tablets of promoted iron-chromium shift catalyst and exposed to a mixture of carbon dioxide, carbon monoxide, steam, hydrogen, and nitrogen. It is demonstrated that carbon monoxide conversion can be enhanced to 100% in the presence of a carbon dioxide sorbent. At breakthrough, carbon monoxide and carbon dioxide simultaneously appear at the end of the bed. During more than 300 cycles of adsorption/reaction and desorption, the capture rate, and carbon monoxide conversion are confirmed to be stable. Two different cycle types are investigated: one cycle with a CO{sub 2} rinse step and one cycle with a steam rinse step. The performance of both SEWGS cycles are discussed.

van Selow, E.R.; Cobden, P.D.; Verbraeken, P.A.; Hufton, J.R.; van den Brink, R.W. [Energy research Center of the Netherlands, Petten (Netherlands)

2009-05-15T23:59:59.000Z

199

Office of Learning and Workforce Development (HC-20) | Department of Energy  

Broader source: Energy.gov (indexed) [DOE]

Learning and Workforce Learning and Workforce Development (HC-20) Office of Learning and Workforce Development (HC-20) Mission Statement and Fuction Statement The mission of the Office of Learning and Workforce Development is to ensure that the Department of Energy workforce possesses the breath of skills and competencies needed in order to successfully accomplish the mission of the agency. The Office of Learning and Workforce Development establishes the vision, strategy and corporate policy to support the Department's talent development requirements. To accomplish its mission, the Office of Learning and Development provides guidance and resources to define and assess critical workforce competencies. The Office also provides strategies to address identified skills gaps. The Department designs, develops, delivers and manages

200

Assembly of large metagenome data sets using a Convey HC-1 hybrid core computer (7th Annual SFAF Meeting, 2012)  

ScienceCinema (OSTI)

Alex Copeland on "Assembly of large metagenome data sets using a Convey HC-1 hybrid core computer" at the 2012 Sequencing, Finishing, Analysis in the Future Meeting held June 5-7, 2012 in Santa Fe, New Mexico.

Copeland, Alex [DOE JGI

2013-02-11T23:59:59.000Z

Note: This page contains sample records for the topic "hc carbon monoxide" 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

Mechanistical studies on the formation and destruction of carbon monoxide (CO), carbon dioxide (CO2), and carbon trioxide (CO3)  

E-Print Network [OSTI]

) in extraterrestrial, low temperature ices. Reactants and products were analyzed on line and in situ via absorption with a 1/r2 dependence, r being the distance from the sun, and thus becomes less important when the outer% H+ , 2% He2+ , and few heavier nuclei; the energy distribution maximum peaks at around 10 MeV where

Kaiser, Ralf I.

202

Crack detection on HC-130H aircraft using low frequency eddy current  

SciTech Connect (OSTI)

An eddy current inspection method was developed at the Federal Aviation Administration`s Airworthiness Assurance NDI Validation Center (AANC) to easily and rapidly detect subsurface fatigue cracks in the wheel well fairing on the US Coast Guard (USCG) HC-130H aircraft caused by fatigue. The inspection procedure locates cracks as small as 10.2 millimeters in length at 2.54 mm below the skin surface at raised fastener sites. The test procedure developed baseline three USCG aircraft. Inspection results on the three aircraft reveals good correlation with results made during subsequent structural disassembly.

Moore, D.G. [Sandia National Labs., Albuquerque, NM (United States); Mihelic, J.E.; Barnes, J.D. [Coast Guard, Elizabeth City, NC (United States). Aircraft Repair and Supply Center

1998-02-01T23:59:59.000Z

203

Table HC6.9 Home Appliances Characteristics by Number of Household Members, 2005  

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

HC6.9 Home Appliances Characteristics by Number of Household Members, 2005 HC6.9 Home Appliances Characteristics by Number of Household Members, 2005 Total U.S.............................................................. 111.1 30.0 34.8 18.4 15.9 12.0 Cooking Appliances Conventional Ovens Use an Oven.................................................. 109.6 29.5 34.4 18.2 15.7 11.8 1................................................................. 103.3 28.4 32.0 17.3 14.7 11.0 2 or More.................................................... 6.2 1.1 2.5 1.0 0.9 0.8 Do Not Use an Oven...................................... 1.5 0.6 0.4 Q Q Q Most-Used Oven Fuel Electric....................................................... 67.9 18.2 22.5 11.2 9.5 6.5 Natural Gas................................................ 36.4 9.9 10.0 6.1 5.6 4.7 Propane/LPG.............................................

204

Experimental evaluation of automotive air-conditioning using HFC-134a and HC-134a  

Science Journals Connector (OSTI)

An experimental study to evaluate the energy consumption of an automotive air conditioning is presented. In this study these refrigerants will be tested using the experimental rig which simulated the actual cars as a cabin complete with a cooling system component of the actual car that is as the blower evaporator condenser radiators electric motor which acts as a vehicle engine and then the electric motor will operate the compressor using a belt and pulley system as well as to the alternator will recharge the battery. The compressor working with the fluids HFC-134a and HC-134a and has been tested varying the speed in the range 1000 1500 2000 and 2500 rpm. The measurements taken during the one hour experimental periods at 2-minutes interval times for temperature setpoint of 20°C with internal heat loads 0 500 700 and 1000 W. The final results of this study show an overall better energy consumption of the HFC-134a compared with the HC-134a.

Azhar Abdul Aziz

2012-01-01T23:59:59.000Z

205

Study of $?(3686)\\to?^0 h_c, h_c\\to??_c$ via $?_c$ exclusive decays  

E-Print Network [OSTI]

The process $\\psi(3686) \\to \\pi^0 h_c, h_c \\to \\gamma \\eta_c$ has been studied with a data sample of $106 \\pm 4$ million $\\psi(3686)$ events collected with the BESIII detector at the BEPCII storage ring. The mass and width of the $P$-wave charmonium spin-singlet state $h_c(^1P_1)$ are determined by simultaneously fitting distributions of the $\\pi^0$ recoil mass for 16 exclusive $\\eta_c$ decay modes. The results, $M(\\hc) = 3525.31 \\pm 0.11 {\\rm (stat.)} \\pm 0.14 {\\rm (syst.)}$\\,MeV/$c^2$ and $\\Gamma(\\hc) = 0.70 \\pm 0.28 \\pm 0.22$\\,MeV, are consistent with and more precise than previous measurements. We also determine the branching ratios for the 16 exclusive $\\eta_c$ decay modes, five of which have not been measured previously. New measurements of the $\\eta_c$ line-shape parameters in the $E1$ transition $h_c\\to\\gamma\\eta_c$ are made by selecting candidates in the $h_c$ signal sample and simultaneously fitting the hadronic mass spectra for the 16 $\\eta_c$ decay channels. The resulting $\\eta_c$ mass and width values are $M(\\eta_c) = 2984.49 \\pm 1.16 \\pm 0.52$\\,MeV/$c^2$ and $\\Gamma(\\eta_c) = 36.4 \\pm 3.2 \\pm 1.7$\\,MeV.

The BESIII Collaboration; M. Ablikim; M. N. Achasov; O. Albayrak; D. J. Ambrose; F. F. An; Q. An; J. Z. Bai; Y. Ban; J. Becker; J. V. Bennett; M. Bertani; J. M. Bian; E. Boger; O. Bondarenko; I. Boyko; R. A. Briere; V. Bytev; X. Cai; O. Cakir; A. Calcaterra; G. F. Cao; S. A. Cetin; J. F. Chang; G. Chelkov; G. Chen; H. S. Chen; J. C. Chen; M. L. Chen; S. J. Chen; X. Chen; Y. B. Chen; H. P. Cheng; Y. P. Chu; D. Cronin-Hennessy; H. L. Dai; J. P. Dai; D. Dedovich; Z. Y. Deng; A. Denig; I. Denysenko; M. Destefanis; W. M. Ding; Y. Ding; L. Y. Dong; M. Y. Dong; S. X. Du; J. Fang; S. S. Fang; L. Fava; F. Feldbauer; C. Q. Feng; R. B. Ferroli; C. D. Fu; J. L. Fu; Y. Gao; C. Geng; K. Goetzen; W. X. Gong; W. Gradl; M. Greco; M. H. Gu; Y. T. Gu; Y. H. Guan; A. Q. Guo; L. B. Guo; Y. P. Guo; Y. L. Han; F. A. Harris; K. L. He; M. He; Z. Y. He; T. Held; Y. K. Heng; Z. L. Hou; H. M. Hu; T. Hu; G. M. Huang; G. S. Huang; J. S. Huang; X. T. Huang; Y. P. Huang; T. Hussain; C. S. Ji; Q. Ji; Q. P. Ji; X. B. Ji; X. L. Ji; L. L. Jiang; X. S. Jiang; J. B. Jiao; Z. Jiao; D. P. Jin; S. Jin; F. F. Jing; N. Kalantar-Nayestanaki; M. Kavatsyuk; W. Kuehn; W. Lai; J. S. Lange; C. H. Li; Cheng Li; Cui Li; D. M. Li; F. Li; G. Li; H. B. Li; J. C. Li; K. Li; Lei Li; Q. J. Li; S. L. Li; W. D. Li; W. G. Li; X. L. Li; X. N. Li; X. Q. Li; X. R. Li; Z. B. Li; H. Liang; Y. F. Liang; Y. T. Liang; G. R. Liao; X. T. Liao; B. J. Liu; C. L. Liu; C. X. Liu; C. Y. Liu; F. H. Liu; Fang Liu; Feng Liu; H. Liu; H. H. Liu; H. M. Liu; H. W. Liu; J. P. Liu; K. Y. Liu; Kai Liu; P. L. Liu; Q. Liu; S. B. Liu; X. Liu; Y. B. Liu; Z. A. Liu; Zhiqiang Liu; Zhiqing Liu; H. Loehner; G. R. Lu; H. J. Lu; J. G. Lu; Q. W. Lu; X. R. Lu; Y. P. Lu; C. L. Luo; M. X. Luo; T. Luo; X. L. Luo; M. Lv; C. L. Ma; F. C. Ma; H. L. Ma; Q. M. Ma; S. Ma; T. Ma; X. Y. Ma; Y. Ma; F. E. Maas; M. Maggiora; Q. A. Malik; Y. J. Mao; Z. P. Mao; J. G. Messchendorp; J. Min; T. J. Min; R. E. Mitchell; X. H. Mo; C. Morales Morales; C. Motzko; N. Yu. Muchnoi; H. Muramatsu; Y. Nefedov; C. Nicholson; I. B. Nikolaev; Z. Ning; S. L. Olsen; Q. Ouyang; S. Pacetti; J. W. Park; M. Pelizaeus; H. P. Peng; K. Peters; J. L. Ping; R. G. Ping; R. Poling; E. Prencipe; M. Qi; S. Qian; C. F. Qiao; X. S. Qin; Y. Qin; Z. H. Qin; J. F. Qiu; K. H. Rashid; G. Rong; X. D. Ruan; A. Sarantsev; B. D. Schaefer; J. Schulze; M. Shao; C. P. Shen; X. Y. Shen; H. Y. Sheng; M. R. Shepherd; X. Y. Song; S. Spataro; B. Spruck; D. H. Sun; G. X. Sun; J. F. Sun; S. S. Sun; Y. J. Sun; Y. Z. Sun; Z. J. Sun; Z. T. Sun; C. J. Tang; X. Tang; I. Tapan; E. H. Thorndike; D. Toth; M. Ullrich; G. S. Varner; B. Wang; B. Q. Wang; D. Wang; D. Y. Wang; K. Wang; L. L. Wang; L. S. Wang; M. Wang; P. Wang; P. L. Wang; Q. Wang; Q. J. Wang; S. G. Wang; X. L. Wang; Y. D. Wang; Y. F. Wang; Y. Q. Wang; Z. Wang; Z. G. Wang; Z. Y. Wang; D. H. Wei; J. B. Wei; P. Weidenkaff; Q. G. Wen; S. P. Wen; M. Werner; U. Wiedner; L. H. Wu; N. Wu; S. X. Wu; W. Wu; Z. Wu; L. G. Xia; Z. J. Xiao; Y. G. Xie; Q. L. Xiu; G. F. Xu; G. M. Xu; H. Xu; Q. J. Xu; X. P. Xu; Z. R. Xu; F. Xue; Z. Xue; L. Yan; W. B. Yan; Y. H. Yan; H. X. Yang; Y. Yang; Y. X. Yang; H. Ye; M. Ye; M. H. Ye; B. X. Yu; C. X. Yu; H. W. Yu; J. S. Yu; S. P. Yu; C. Z. Yuan; Y. Yuan; A. A. Zafar; A. Zallo; Y. Zeng; B. X. Zhang; B. Y. Zhang; C. Zhang; C. C. Zhang; D. H. Zhang; H. H. Zhang; H. Y. Zhang; J. Q. Zhang; J. W. Zhang; J. Y. Zhang; J. Z. Zhang; S. H. Zhang; X. J. Zhang; X. Y. Zhang; Y. Zhang; Y. H. Zhang; Y. S. Zhang; Z. P. Zhang; Z. Y. Zhang; G. Zhao; H. S. Zhao; J. W. Zhao; K. X. Zhao; Lei Zhao; Ling Zhao; M. G. Zhao; Q. Zhao; Q. Z. Zhao; S. J. Zhao; T. C. Zhao; X. H. Zhao; Y. B. Zhao; Z. G. Zhao; A. Zhemchugov; B. Zheng; J. P. Zheng; Y. H. Zheng; B. Zhong; J. Zhong; Z. Zhong; L. Zhou; X. K. Zhou; X. R. Zhou; C. Zhu; K. Zhu; K. J. Zhu; S. H. Zhu; X. L. Zhu; Y. C. Zhu; Y. M. Zhu; Y. S. Zhu; Z. A. Zhu; J. Zhuang; B. S. Zou; J. H. Zou

2012-09-22T23:59:59.000Z

206

Catalysis of hydrocarbon synthesis from CO and H{sub 2} on carbon membranes  

SciTech Connect (OSTI)

This paper describes the preparation of carbon membrane supports from polyacrylonitrile. The membranes were utilized for the preparation of cobalt catalysts. The catalysts were prepared by impregnating the membranes with a cobalt nitrate solution followed by drying on a water bath. The cobalt was sometimes introduced directly into the molding solution before the activation stage. The cobalt catalysts were utilized in the methanation of carbon monoxide. The products were dependent on the conditions utilized to obtain the carbon supports.

Lapidus, A.l.; Krylova, A.Yu.; Strupov, A.N.; Linkov, V.M.; Sanderson, R.D. [Rossiiskaya Akademiya, Nauk (Russian Federation)

1994-12-31T23:59:59.000Z

207

Experimental flight test vibration measurements and nondestructive inspection on a USCG HC-130H aircraft  

SciTech Connect (OSTI)

This paper presents results of experimental flight test vibration measurements and structural inspections performed by the Federal Aviation Administration`s Airworthiness Assurance NDI Validation Center (AANC) at Sandia National Laboratories and the US Coast Guard Aircraft Repair and Supply Center (ARSC). Structural and aerodynamic changes induced by mounting a Forward Looking Infrared (FLIR) system on a USCG HC-130H aircraft are described. The FLIR adversely affected the air flow characteristics and structural vibration on the external skin of the aircraft`s right main wheel well fairing. Upon initial discovery of skin cracking and visual observation of skin vibration in flight by the FLIR, a baseline flight without the FLIR was conducted and compared to other measurements with the FLIR installed. Nondestructive inspection procedures were developed to detect cracks in the skin and supporting structural elements and document the initial structural condition of the aircraft. Inspection results and flight test vibration data revealed that the FLIR created higher than expected flight loading and was the possible source of the skin cracking. The Coast Guard performed significant structural repair and enhancement on this aircraft, and additional in-flight vibration measurements were collected on the strengthened area both with and without the FLIR installed. After three months of further operational FLIR usage, the new aircraft skin with the enhanced structural modification was reinspected and found to be free of flaws. Additional US Coast Guard HC-130H aircraft are now being similarly modified to accommodate this FLIR system. Measurements of in-flight vibration levels with and without the FLIR installed, and both before and after the structural enhancement and repair were conducted on the skin and supporting structure in the aircraft`s right main wheel fairing. Inspection results and techniques developed to verify the aircraft`s structural integrity are discussed.

Moore, D.G.; Jones, C.R. [Sandia National Labs., Albuquerque, NM (United States). FAA Airworthiness Assurance NDI Validation Center; Mihelic, J.E.; Barnes, J.D. [Coast Guard Aircraft Repair and Supply Center, Elizabeth City, NC (United States)

1998-08-01T23:59:59.000Z

208

CSER 00-008 use of PFP Glovebox HC-18BS for Storage and Transport of Fissionable Material  

SciTech Connect (OSTI)

This CSER addresses the feasibility of increasing the allowed number of open containers and permitting the transfer and storage of fissionable material in Glovebox HC-18BS without regard to form or density (metal, oxide having an H/X {le} 20, material having unrestricted moderation and plutonium hydroxide having a plutonium density of 0.2 g/cm{sup 3}).

ERICKSON, D.G.

2000-06-01T23:59:59.000Z

209

Carbon Dioxide Hydrate Process for Gas Separation from a Shifted Synthesis Gas Stream  

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

Sequestration and Sequestration and Gasification Technologies Carbon DioxiDe HyDrate ProCess for Gas seParation from a sHifteD syntHesis Gas stream Background One approach to de-carbonizing coal is to gasify it to form fuel gas consisting predominately of carbon monoxide and hydrogen. This fuel gas is sent to a shift conversion reactor where carbon monoxide reacts with steam to produce carbon dioxide (CO 2 ) and hydrogen. After scrubbing the CO 2 from the fuel, a stream of almost pure hydrogen stream remains, which can be burned in a gas turbine or used to power a fuel cell with essentially zero emissions. However, for this approach to be practical, it will require an economical means of separating CO 2 from mixed gas streams. Since viable options for sequestration or reuse of CO

210

Adsorption and methanation of carbon dioxide on a nickel/silica catalyst  

SciTech Connect (OSTI)

Temperature-programed desorption and reaction studies showed that increasing amounts of CO/sub 2/ adsorbed on silica-supported 6.9% nickel with increasing temperature to a maximum adsorption at approx. 443/sup 0/K, i.e., that the adsorption was activated; that CO/sub 2/ desorbed partly as CO/sub 2/ with the peak at 543/sup 0/K, and partly as CO with several peaks; that in the presence of hydrogen, nearly all adsorbed CO/sub 2/ desorbed as methane, and a small amount as CO; and that the methane desorption peaks from adsorbed CO and CO/sub 2/ both occurred at 473/sup 0/K. These results suggested that carbon dioxide adsorbed dissociatively as a carbon monoxide and an oxygen species. An observed absence of higher hydrocarbons in the methanation products of carbon dioxide was attributed to a high hydrogen/carbon monoxide surface ratio caused by the activated carbon dioxide adsorption.

Falconer, J.L.; Zagli, A.E.

1980-04-01T23:59:59.000Z

211

Titanium monoxide spectroscopy following laser-induced optical breakdown  

SciTech Connect (OSTI)

This work investigates Titanium Monoxide (TiO) in ablation-plasma by employing laser-induced breakdown spectroscopy (LIBS) with 1 to 10 TW/cm{sup 2} irradiance, pulsed, 13 nanosecond, Q-switched Nd:YAG laser radiation at the fundamental wavelength of 1064 nm. The analysis of TiO is based on our first accurate determination of transition line strengths for selected TiO A-X, B-X, and E-X transitions, particularly TiO A-X {gamma} and B-X {gamma} Prime bands. Electric dipole line strengths for the A{sup 3}{Phi}-X{sup 3}{delta} and B{sup 3}{Pi}-X{sup 3}{delta} bands of TiO are computed. The molecular TiO spectra are observed subsequent to laser-induced breakdown (LIB). We discuss analysis of diatomic molecular spectra that may occur simultaneously with spectra originating from atomic species. Gated detection is applied to investigate the development in time of the emission spectra following LIB. Collected emission spectra allow one to infer micro-plasma parameters such as temperature and electron density. Insight into the state of the micro-plasma is gained by comparing measurements with predictions of atomic and molecular spectra. Nonlinear fitting of recorded and computed diatomic spectra provides the basis for molecular diagnostics, while atomic species may overlap and are simultaneously identified. Molecular diagnostic approaches similar to TiO have been performed for diatomic molecules such as AlO, C{sub 2}, CN, CH, N{sub 2}, NH, NO and OH.

Parigger, Christian G.; Woods, Alexander C.; Keszler, Anna; Nemes, Laszlo; Hornkohl, James O. [The University of Tennessee/UT Space Institute, Center for Laser Applications, 411 B.H. Goethert Parkway, Tullahoma, TN 37388-9700 (United States); Chemical Research Center of the Hungarian Academy of Sciences, Institute of Materials and Environmental Chemistry, Pusztaszeri ut 59-67, H-1025 Budapest (Hungary); Chemical Research Center of the Hungarian Academy of Sciences, Laser Spectroscopy Laboratory, Pusztaszeri ut 59-67, H-1025 Budapest (Hungary); Hornkohl Consulting, Tullahoma, TN 37388 (United States)

2012-07-30T23:59:59.000Z

212

Synthesis of higher alcohols from carbon monoxide and hydrogen in a slurry reactor  

SciTech Connect (OSTI)

Higher, i.e. C{sub 2{sup +}}, alcohols are desired as gasoline additives, feedstocks for producing ethers and as alternative fuels for automobiles. In all cases, the backbone branching of an alcohol improves octane rating, which is essential for good engine performance. These types of branched, higher alcohols are the desired products for a process converting synthesis gas, a CO and H{sub 2} mixture, often generated from coal gasification. Based on this premise, promoted ZnCr oxide catalysts appear to be as one of the best avenues for further investigation. Once this investigation is complete, a natural extension is to replace the Cr in the ZnCr oxide catalyst with Mo and W, both in the same elemental triad with Cr. Mo has already been shown as an active HAS catalyst, both on a SiO{sub 2} support and in the MoS{sub 2} form. The three catalyst combinations, ZnMo, ZnW, and MnCr oxides will be tested in the stirred autoclave system. However, if none of the three indicate any comparable activity and/or selectivity toward higher alcohols as compared with other HAS catalysts, then an investigation of the effects of Cs promotion on the ZnCr oxide methanol catalysts will be executed.

McCutchen, M.S.

1992-08-28T23:59:59.000Z

213

A Novel Carbon Monoxide-Releasing Molecule Fully Protects Mice from Severe Malaria  

Science Journals Connector (OSTI)

...exudate, and elevated VEGF levels in plasma, followed by death between days 7 and...b) Levels of VEGF protein in the plasma of P. berghei ANKA-infected DBA-2...adequate cautions. Published ahead of print 12 December 2011 Supplemental material...

Ana C. Pena; Nuno Penacho; Liliana Mancio-Silva; Rita Neres; João D. Seixas; Afonso C. Fernandes; Carlos C. Romão; Maria M. Mota; Gonçalo J. L. Bernardes; Ana Pamplona

2011-12-12T23:59:59.000Z

214

A Novel Carbon Monoxide-Releasing Molecule Fully Protects Mice from Severe Malaria  

Science Journals Connector (OSTI)

...temperature under a nitrogen atmosphere. The solution was concentrated...C O) cm deltaH (400 MHz, D2O) 2.23 (3H...an inductively coupled plasma-atomic emission spectrometer...growth factor (VEGF) in plasma samples was determined...elevated VEGF levels in plasma, followed by death between...

Ana C. Pena; Nuno Penacho; Liliana Mancio-Silva; Rita Neres; João D. Seixas; Afonso C. Fernandes; Carlos C. Romão; Maria M. Mota; Gonçalo J. L. Bernardes; Ana Pamplona

2011-12-12T23:59:59.000Z

215

Measuring the Kinetics of the Reduction of Iron Oxide with Carbon Monoxide in a Fluidized Bed  

Science Journals Connector (OSTI)

Combusting a solid fuel in the presence of a metal oxide rather than air, chemical looping combustion, generates CO2suitable for sequestration and the reduced metal. For the case of iron, the reduced oxide can be...

C. D. Bohnt; J. P. Cleeton; C. M. Miiller…

2010-01-01T23:59:59.000Z

216

Detection of carbon monoxide (CO) as a furnace byproduct using a rotating mask spectrometer.  

SciTech Connect (OSTI)

Sandia National Laboratories, in partnership with the Consumer Product Safety Commission (CPSC), has developed an optical-based sensor for the detection of CO in appliances such as residential furnaces. The device is correlation radiometer based on detection of the difference signal between the transmission spectrum of the sample multiplied by two alternating synthetic spectra (called Eigen spectra). These Eigen spectra are derived from a priori knowledge of the interferents present in the exhaust stream. They may be determined empirically for simple spectra, or using a singular value decomposition algorithm for more complex spectra. Data is presented on the details of the design of the instrument and Eigen spectra along with results from detection of CO in background N{sub 2}, and CO in N{sub 2} with large quantities of interferent CO{sub 2}. Results indicate that using the Eigen spectra technique, CO can be measured at levels well below acceptable limits in the presence of strongly interfering species. In addition, a conceptual design is presented for reducing the complexity and cost of the instrument to a level compatible with consumer products.

Sinclair, Michael B.; Flemming, Jeb Hunter; Blair, Raymond (Honeywell Federal Manufacturing & Technologies, Albuqueruque, NM); Pfeifer, Kent Bryant

2006-02-01T23:59:59.000Z

217

Test results of a ceramic-based carbon monoxide sensor in the automotive exhaust manifold  

SciTech Connect (OSTI)

A prototype CO sensor based on the anatase phase of TiO{sub 2} was fabricated and tested in a Ford V6 engine. Fuel combustion was programmed to be near stoichiometric conditions, and emissions were monitored with an FT-IR analytical instrument. The sensor, positioned near the oxygen sensor in the exhaust manifold, was successfully tested for 50 cycles of revving and idling, and was observed to respond quickly and reproducibly. The sensor response was correlated to the CO concentration at specific engine temperatures and was found to vary systematically with increasing concentrations. The results are promising and the sensor shows potentials to monitor the efficiency of the catalytic converter.

Azad, A.M.; Younkman, L.B.; Akbar, S.A. [Ohio State Univ., Columbus, OH (United States)

1996-12-31T23:59:59.000Z

218

Sensing mechanism of a carbon monoxide sensor based on anatase titania  

SciTech Connect (OSTI)

This paper reports results on a TiO{sub 2} (anatase)-based CO sensor and proposes a possible surface-controlled sensing mechanism. The complex plane analysis of the ac electrical data provides quantitative evidence supporting the mechanism. The grain-boundary capacitance and conductance, extracted from the impedance plane, were observed to increase with the CO concentration. This effect is attributed to a change in the depletion region thickness and barrier height at the TiO{sub 2} intergranular contact. The analysis of the electrical data combined with x-ray diffraction and x-ray photoelectron spectroscopy observations support the proposed sensing mechanism involving CO adsorption and ionization on the titania surface, and not an oxidation-reduction type reaction as observed in most oxide-based sensors.

Akbar, S.A.; Younkman, L.B. [Ohio State Univ., Columbus, OH (United States). Dept. of Materials Science and Engineering

1997-05-01T23:59:59.000Z

219

Adsorption effects during temperature-programmed desorption of carbon monoxide from supported platinum  

SciTech Connect (OSTI)

To investigate the effects of CO adsorption, we develop a mathematical model and use it to compute desorption spectra for the TPD of CO from Pt dispersed over a porous support into (a) an inert carrier gas and (b) a vacuum. Over the realistic parameter range considered, our model predicts that adsorption effects, caused by high concentrations of gaseous CO in the system, are always an important feature, broadening the desorption peaks and shifting them to higher temperatures. Indeed, we find that adsorption competes with desorption to the extent that adsorption equilibrium is always approached closely within the porous supported Pt samples. For desorption into a carrier gas, the adsorption effects result from limitations to the flow of CO from the sample cell, whereas for desorption into a vacuum, the adsorption effects result from limitations to the diffusion of CO from the porous sample. Our results suggest that significant adsorption effects will also be present during the TPD of CO from other Group VIII precious metals dispersed over porous supports. 4 figures, 2 tables.

Herz, R.K.; Kiela, J.B.; Marin, S.P.

1982-01-01T23:59:59.000Z

220

Some general laws of the hydrogenation of carbon monoxide on metals  

SciTech Connect (OSTI)

The catalytic properties of supported transition metals in the hydrogenation of CO to hydrocarbons have been studied. A kinetic model interpreting the unusual dependence of the activation energy on temperature is proposed. It is shown that the catalytic activity (r) decreases and the selectivity with respect to methane (SCH/sub 4/) increases with an increase in the heat of adsorption of CO.

Golodets, G.I.; Pavlenko, N.V.; Tripol'skii, A.I.

1988-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "hc carbon monoxide" 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

Kinetic study of the reaction between nitric oxide and carbon monoxide catalyzed by clean polycrystalline platinum  

SciTech Connect (OSTI)

The kinetics of the platinum catalyzed reaction between NO and CO has been studied under conditions chosen to approximate those observed during operation of catalysts in automotive exhaust gas treatment applications. The catalysts were polycrystalline platinum foils and wires. The reaction was studied over a range of reactant partial pressures of 10 V Torr to 1 Torr and catalyst temperatures of 500 to 1500K. The steady-state kinetics results could not be fit by a simple Langmuir-Hinshelwood kinetic model over all experimental conditions studied. The kinetics at high coverage were most consistent with Langmuir-Hinshelwood kinetics assuming a bimolecular reaction between NO and CO as the rate-limiting step. At high temperature, the Langmuir-Hinshelwood assumption of fast adsorption-desorption equilibrium relative to the surface reaction rate was no longer appropriate and the mechanism of adsorption of NO had to be considered explicitly.

Klein, R.L.

1984-01-01T23:59:59.000Z

222

Dissociation and oxidation of carbon monoxide over Rh/Al sub 2 O sub 3 catalysts  

SciTech Connect (OSTI)

The activity of Rh/Al{sub 2}O{sub 3} catalysts for CO oxidation was investigated by transient isotopic pulse experiments using packed-bed reactor. This transient experimental scheme revealed significant CO dissociation activity during CO oxidation over Rh/Al{sub 2}O{sub 3} catalysts. Results indicate that the oxidation of CO proceeds via dissociative oxidation by its own oxygen as well as via direct oxidation by gas-phase oxygen on well-dispersed Rh/Al{sub 2}O{sub 3} catalysts. The rate of CO dissociation is on the same order of magnitude as the rate of CO oxidation; under steady-state conditions at 300{degree}C, the rate of CO dissociation is approximately half that of direct oxidation. Differences in CO dissociation activity between single-crystal Rh surfaces and well-dispersed supported Rh particles are explained in terms of the molecular bonding and adsorption characteristics on these two different surfaces. The importance of CO dissociation kinetics in the overall CO oxidation activity of Rh/Al{sub 2}O{sub 3} catalysts is further discussed in view of the reaction lightoff behavior.

Cho, Byong K.; Stock, C.J. (General Motors Research Labs., Warren, MI (USA))

1989-05-01T23:59:59.000Z

223

Adsorption of carbon monoxide on ZSM-5 zeolites. Infrared spectroscopic study and quantum-chemical calculations  

SciTech Connect (OSTI)

Low temperature adsorption of CO was studied on H-ZSM-5 zeolites modified by dehydroxylation, ionic exchange with Al/sup 3 +/, and impregnation with Al/sub 2/O/sub 3/ and on Na-ZSM-5 and CaH-ZSM-5 zeolites. It was found that interaction of CO with framework OH groups results in the formation of a hydrogen-bonded CO complex whose OH bond frequency is decreased by 310-320 cm/sup -1/ compared with that of free hydroxyls. For the less acidic framework hydroxyls in large cavities of H/sub 70/Na/sub 30/-Y zeolite the observed shift is 275 cm/sup -1/. With ZSM-5 zeolites, at least six types of electron-accepting sites are observed originating from nonframework Al species (band of CO in the interaction complex: 2132, 2222, 2202, 2195, and 2198 cm/sup -1/) and the Al/sub 2/O/sub 3/ microcrystalline phase (CO band at 2153 cm/sup -1/). The CO bond orders calculated by the CNDO/2 method for the CO interaction complexes with models of surface sites increase in the following order: > O-CO < > OH-CO approx. ..-->.. Al-CO approx. = Na-CO < alumina-CO approx. = Ca-CO < ..-->.. Si-CO < Al(cationic)-CO. A correlation between the calculated bond orders of CO and the observed vibrational frequencies of CO-forming interaction complexes is drawn.

Kustov, L.M.; Kazansky, V.B.; Beran, S.; Kubelkova, L.; Jiru, P.

1987-09-24T23:59:59.000Z

224

Sulfur adsorption on nickel(100) and its effect on carbon monoxide, nitric oxide, and deuterium chemisorption  

SciTech Connect (OSTI)

The adsorption of CO, NO, and D/sub 2/ was studied on clean and sulfided Ni(100) near 100K using Auger electron spectroscopy, thermal desorption spectroscopy, X-ray and ultraviolet photoelectron spectroscopies, and work function change measurements. The evidence suggests that sulfur's effects are predominantly steric in nature. Weak, short-range (approx.4 angstrom) electrostatic effects are also present, due to charge transfer of about 0.04 of an electron from nickel to sulfur. The blocking effect of S on the adsorption of each gas at various temperatures is discussed.

Hardegree, E.L.

1985-01-01T23:59:59.000Z

225

Free-radical reactions in glow and explosion of carbon monoxide-oxygen mixtures  

SciTech Connect (OSTI)

Examination of published compilations of rate coefficients of free-radical reactions yields reactions that are associated with chain branching in mixtures of CO and O/sub 2/ and small quantities of hydrogen or water vapor. The complete mechanism included diffusion of HO/sub 2/ radicals to the vessel wall and their adsorption and reaction at the surface. This mechanism is applied to the data of E.J. Buckler and R.G.W. Norrish on the branched-chain explosion of CO-O/sub 2/ mixtures containing H/sub 2/ in the order of 1 mm Hg. Substantial agreement is found between theory and experiment. Further, the mechanism is applied to experiments of Bond, Gray, and Griffiths with an H/sub 2/ content of 0.01-0.05 mm Hg. By specifying details of the adsorption and surface reaction of HO/sub 2/ on the basis of Langmuir's adsorption the phenomenon of flow is explained and the regions of slow reaction, glow, and explosion are described in accord with the experimental data. It is confirmed that the reaction between CO and O/sub 2/ requires the presence of a hydrogenous compound such as H/sub 2/, H/sub 2/O, CH/sub 4/, etc., and that ''dry'' homogenous reaction is not possible except at very high temperatures.

Von Elbe, G.; Lewis, B.

1986-02-01T23:59:59.000Z

226

Homologation and functionalization of carbon monoxide by a recyclable uranium complex  

Science Journals Connector (OSTI)

...C-5b (R = Ph) were confirmed by CHN combustion analyses, FTIR spectroscopy, and the...SiOCCOSiPh 3 , and 4 to estimate the heats of formation ({delta}H for ) for...resource from which to produce industrial hydrocarbon feedstocks as alternatives to crude oil...

Benedict M. Gardner; John C. Stewart; Adrienne L. Davis; Jonathan McMaster; William Lewis; Alexander J. Blake; Stephen T. Liddle

2012-01-01T23:59:59.000Z

227

Impacts of 2006 Indonesian fires and dynamics on tropical upper tropospheric carbon monoxide and ozone  

E-Print Network [OSTI]

reproduce seasonal mean lightning flash rates to match theobser- vations of lightning flashes from the Optical

2011-01-01T23:59:59.000Z

228

Hydrocarbons from carbon monoxide hydrogen-steam mixtures, unusual product distributions and mechanistic implications  

SciTech Connect (OSTI)

Over recent years, considerable interest has developed in hydrocarbon synthesis via direct processing of H/sub 2/-lean synthesis gases which are produced by the ''second generation'' of thermally efficient coal gasifiers. To directly process gases with a H/sub 2//CO ratio less than 0.5, requires that water be mixed with the reactor feed gas so that additional H/sub 2/ is generated in-situ via the water-gas-shift (WGS) reaction. This obviously requires the use of catalysts which are active for both the synthesis and WGS reactions. The fact that most Group VIII metals are active for both reactions is well demonstrated by the development of the Kolbel-Engelhardt (KE) synthesis in which all the H/sub 2/ is formed in-situ. The authors previously examined the effect of H/sub 2//CO/H/sub 2/2O feed ratios on CO conversion rates (4); the present report concerns its effect upon hydrocarbon product distributions. In the experiments described, as the H/sub 2//CO ratio was reduced from 2.0 (Typical Fischer-Tropsch (FT) conditions), sufficient H/sub 2/O was added to compensate for the H/sub 2/ deficiency based on the assumption that all added H/sub 2/O was converted to H/sub 2/ via the WGS reaction.

Chaffee, A.L.; Ekstrom; Lapszewica, J.; Loeh, H.

1986-03-01T23:59:59.000Z

229

Multimodel simulations of carbon monoxide: Comparison with observations and projected near-future changes  

E-Print Network [OSTI]

development of a gridded climatology for tropospheric ozone,et al. , 2000] O 3 climatology based on satellite and sondeO 3 nudged toward climatology above 380 K zonal mean O 3

2006-01-01T23:59:59.000Z

230

Nitric oxide and carbon monoxide in cigarette smoke in the development of cardiorespiratory disease in smokers  

E-Print Network [OSTI]

(Rep 1983). This could be due to indoor air pollution but respiratory disease in childhood may affect later respiratory function ( Burrows, Knudson and Lebvitz 1977). Similarly the decline in bronchitis mortality i n the U.K . in re c ent years which... anteceded the decline in cigarette cons umption might, in addition, suggest an effect of outdoor pollution Air Acts". The marked internat ional differences in mortality and the high figures for the British I sles...

Borland, Colin David Ross

1988-10-18T23:59:59.000Z

231

TEXIN2: a model for predicting carbon monoxide concentrations near intersections  

E-Print Network [OSTI]

of the Journal of the Air Pollution Control Association emitted along straight roadways, where traffic is wel 1-def ined and flows uniformly at constant speeds. This scenario is extremely inap- propriate for intersections. A simple conversion from straight... are presented in Chapter V. CHAPTER II LITERATURE REVIEW The task of modeling pollutant concentrations near intersections has traditionally been approached by first enlisting an emissions model to estimate a composite emission rate for vehicular traffic...

Korpics, J. J

1985-01-01T23:59:59.000Z

232

REFORMULATION OF COAL-DERIVED TRANSPORTATION FUELS: SELECTIVE OXIDATION OF CARBON MONOXIDE ON METAL FOAM CATALYSTS  

SciTech Connect (OSTI)

Hydrocarbon fuels must be reformed in a series of steps to provide hydrogen for use in proton exchange membrane fuel cells (PEMFCs). Preferential oxidation (PROX) is one method to reduce the CO concentration to less than 10 ppm in the presence of {approx}40% H{sub 2}, CO{sub 2}, and steam. This will prevent CO poisoning of the PEMFC anode. Structured supports, such as ceramic monoliths, can be used for the PROX reaction. Alternatively, metal foams offer a number of advantages over the traditional ceramic monolith.

Paul Chin; Xiaolei Sun; George W. Roberts; Amornmart Sirijarhuphan; Sourabh Pansare; James G. Goodwin Jr; Richard W. Rice; James J. Spivey

2005-06-01T23:59:59.000Z

233

Influence of solid fuel on the carbon-monoxide and nitrogen-oxide emissions on sintering  

SciTech Connect (OSTI)

Laboratory and industrial research now underway at the sintering plant of AO Mittal Steel Temirtau is focusing on the preparation of fuel of optimal granulometric composition, the replacement of coke fines, and the adaptation of fuel-input technology so as to reduce fuel consumption and toxic emissions without loss of sinter quality.

M.F. Vitushchenko; N.L. Tatarkin; A.I. Kuznetsov; A.E. Vilkov [AO Mittal Steel Temirtau, Temirtau (Kazakhstan)

2007-07-01T23:59:59.000Z

234

Electroreduction of carbon monoxide to liquid fuel on oxide-derived nanocrystalline copper  

Science Journals Connector (OSTI)

... were used without further purification. Electrolyte solutions were prepared with deionized water (Ricca Chemical, ASTM Type I). Preparation of oxide-derived Cu 1

Christina W. Li; Jim Ciston; Matthew W. Kanan

2014-04-09T23:59:59.000Z

235

Isotope effect in the formation of carbon monoxide by radiative association  

Science Journals Connector (OSTI)

......levels of the final electronic state. 3 COMPUTATIONAL...parameters needed for calculation of according to...through reaction (2) does not vary much at...1sigma+ transition does not go above 2...curve of the A 1pi electronic state leads to the...M. Mathematical Handbook for Scientists and......

Sergey V. Antipov; Magnus Gustafsson; Gunnar Nyman

2013-01-01T23:59:59.000Z

236

Carbon Monoxide Dehydrogenases and Acetyl-CoA Synthases: Light at the End of the Tunnel?  

SciTech Connect (OSTI)

OAK-B135 Metalloenzymes seem to ''come of age'' when their structures are known at atomic resolution, spectroscopic and catalytic properties are basically understood, and genetic expression systems are available. Such foundations allow detailed mechanistic and spectroscopic properties to be probed and correlated to structure. The objective of this article is to summarize what is known about the title group of enzymes, and show that, to a large degree, they have come of age.

Paul A. Lindahl

2002-02-19T23:59:59.000Z

237

Oxygen isotope fractionation in the vacuum ultraviolet photodissociation of carbon monoxide: Wavelength, pressure and temperature dependency.  

E-Print Network [OSTI]

Oxygen isotope fractionation in the vacuum ultravioletmeasurement of the associated oxygen isotopic composition ofwavelength dependency of the oxygen isotopic composition in

Chakraborty, Subrata

2013-01-01T23:59:59.000Z

238

Carbon Monoxide Pollution Promotes Cardiac Remodeling and Ventricular Arrhythmia in Healthy Rats  

E-Print Network [OSTI]

worldwide by outdoor air pollution caused by vehicles and industrial emissions (http://www.who.int; http:// www.infoforhealth.org). Notably, air pollution increases the risk of mortality from cardiovascular investigating the effects of urban air pollution in humans are mainly restricted to epide- miological studies

Boyer, Edmond

239

REFORMULATION OF COAL-DERIVED TRANSPORTATION FUELS: SELECTIVE OXIDATION OF CARBON MONOXIDE ON METAL FOAM CATALYSTS  

SciTech Connect (OSTI)

Uses for structured catalytic supports, such as ceramic straight-channel monoliths and ceramic foams, have been established for a long time. One of the most prominent examples is the washcoated ceramic monolith as a three-way catalytic converter for gasoline-powered automobiles. A distinct alternative to the ceramic monolith is the metal foam, with potential use in fuel cell-powered automobiles. The metal foams are characterized by their pores per inch (ppi) and density ({rho}). In previous research, using 5 wt% platinum (Pt) and 0.5 wt% iron (Fe) catalysts, washcoated metal foams, 5.08 cm in length and 2.54 cm in diameter, of both varying and similar ppi and {rho} were tested for their activity (X{sub CO}) and selectivity (S{sub CO}) on a CO preferential oxidation (PROX) reaction in the presence of a H{sub 2}-rich gas stream. The variances in these metal foams' activity and selectivity were much larger than expected. Other structured supports with 5 wt% Pt, 0-1 wt% Fe weight loading were also examined. A theory for this phenomenon states that even though these structured supports have a similar nominal catalyst weight loading, only a certain percentage of the Pt/Fe catalyst is exposed on the surface as an active site for CO adsorption. We will use two techniques, pulse chemisorption and temperature programmed desorption (TPD), to characterize our structured supports. Active metal count, metal dispersion, and other calculations will help clarify the causes for the activity and selectivity variations between the supports. Results on ceramic monoliths show that a higher Fe loading yields a lower dispersion, potentially because of Fe inhibition of the Pt surface for CO adsorption. This theory is used to explain the reason for activity and selectivity differences for varying ppi and {rho} metal foams; less active and selective metal foams have a lower Fe loading, which justifies their higher metal dispersion. Data on the CO desorption temperature and average metal crystallite size for TPD are also collected.

Paul Chin; George W. Roberts; James J. Spivey

2003-12-31T23:59:59.000Z

240

INFRARED ABSORPTION SPECTROSCOPY OF CARBON MONOXIDE ON NICKEL FILMS: A LOW TEMPERATURE THERMAL DETECTION TECHNIQUE  

E-Print Network [OSTI]

excess noise from the thermometer element and the digitizingXBL 78/2-6334 Fig. 14. Noise spectra of sample thermometer.noise spectrum of the thermometer signal for two different

Bailey, Robert Brian

2011-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "hc carbon monoxide" 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

Reaction of titanium polonides with carbon dioxide  

SciTech Connect (OSTI)

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

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

1987-05-01T23:59:59.000Z

242

"Table HC4.9 Home Appliances Characteristics by Renter-Occupied Housing Unit, 2005"  

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

HC4.9 Home Appliances Characteristics by Renter-Occupied Housing Unit, 2005" HC4.9 Home Appliances Characteristics by Renter-Occupied Housing Unit, 2005" " Million U.S. Housing Units" ,," Renter-Occupied Housing Units (millions)","Type of Renter-Occupied Housing Unit" ,"U.S. Housing Units (millions" ,,,"Single-Family Units",,"Apartments in Buildings With--" "Home Appliances Characteristics",,,"Detached","Attached","2 to 4 Units","5 or More Units","Mobile Homes" "Total U.S.",111.1,33,8,3.4,5.9,14.4,1.2 "Cooking Appliances" "Conventional Ovens" "Use an Oven",109.6,32.3,7.9,3.3,5.9,14.1,1.1 "1.",103.3,31.4,7.6,3.3,5.7,13.7,1.1 "2 or More",6.2,0.9,0.3,"Q","Q",0.4,"Q"

243

"Table HC3.9 Home Appliances Characteristics by Owner-Occupied Housing Unit, 2005"  

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

HC3.9 Home Appliances Characteristics by Owner-Occupied Housing Unit, 2005" HC3.9 Home Appliances Characteristics by Owner-Occupied Housing Unit, 2005" " Million U.S. Housing Units" ,," Owner-Occupied Housing Units (millions)","Type of Owner-Occupied Housing Unit" ,"U.S. Housing Units (millions" ,,,"Single-Family Units",,"Apartments in Buildings With--" "Home Appliances Characteristics",,,"Detached","Attached","2 to 4 Units","5 or More Units","Mobile Homes" "Total U.S.",111.1,78.1,64.1,4.2,1.8,2.3,5.7 "Cooking Appliances" "Conventional Ovens" "Use an Oven",109.6,77.3,63.4,4.1,1.8,2.3,5.6 "1.",103.3,71.9,58.6,3.9,1.6,2.2,5.5 "2 or More",6.2,5.4,4.8,"Q","Q","Q","Q"

244

Estimation of Carbon Monoxide and Carbon Dioxide at Sub-ppm Level Concentrations in Ammonia Synthesis Gas  

Science Journals Connector (OSTI)

......can be handled per analysis. The ammonia synthesis...conditioning of I2O5 reactors or to marginal flow...20%. Thus, the reliability of the method depends...practice for the analysis of trace impurities...estimated from a single analysis the method of converting...to CO2 using I2O5 reactor (11) after its......

K. Annaji Rao; K.K. Pushpa; Hari Mohan; R.M. Iyer

1978-07-01T23:59:59.000Z

245

Remote Sensing of Commercial Aircraft Emissions Peter J. Popp & Donald H. Stedman  

E-Print Network [OSTI]

), and nitrogen oxides (NOx, which is the sum of nitrogen oxide, NO, and nitrogen dioxide, NO2) emitted from,4 The instrument consists of a non-dispersive infrared (IR) component for detecting carbon monoxide, carbon dioxide (CO2), and hydrocarbons (HC), and a dispersive ultraviolet (UV) spectrometer for measuring nitrogen

Denver, University of

246

Effect of potassium carbonate on char gasification by carbon dioxide  

SciTech Connect (OSTI)

A differential packed-bed reactor has been employed to study the gasification of 7.5 wt% K/sub 2/CO/sub 3/-catalyzed Saran char in carbon dioxide/carbon monoxide mixtures at a total pressure near 1 atm (101.3 kPa) and temperatures between 922 and 1046 K. The rate data were tested with a model which involves two-site adsorption and subsequent dissociation of CO/sub 2/ on the char surface. The results indicate that this model adequately explains the catalyzed gasification data. Moreover, the activation energy for desorption of carbon-oxygen complex is lower for the catalyzed case than for the uncatalyzed case. Adsorption of CO and CO/sub 2/ on both catalyzed and uncatalyzed chars was also followed with a volumetric adsorption apparatus at pressures between 1 and 100 kPa and temperatures from 273 to 725 K. The catalyzed char adsorbed an order of magnitude more CO/sub 2/ at 560 K than the uncatalyzed char. Subsequent dissociation of CO/sub 2/ on the carbon surface does not appear to be catalyzed by potassium. Thus, the catalyst's role is to enhance CO/sub 2/ adsorption, thereby creating more oxygen on the surface, and lowering the activation energy for desorption of the resultant carbon-oxygen species.

Koenig, P.C.; Squires, R.G.; Laurendeau, N.M.

1986-07-01T23:59:59.000Z

247

Dissociation and excitation coefficients of nitrogen molecules and nitrogen monoxide generation  

SciTech Connect (OSTI)

The excitation coefficient ?{sub N2} is calculated for the excited metastable level of N{sub 2}(A{sub 3}?{sub u}{sup +}) in nitrogen molecules. In addition, the dissociation coefficient of nitrogen molecules is investigated by making use of the Boltzmann distribution of the electrons in atmospheric plasmas. The excitation and electron-impact dissociation coefficients of nitrogen molecules are analytically expressed in terms of the electron temperature T{sub e} for evaluations of the reactive oxygen and nitrogen species in atmospheric plasmas. As an application example of these coefficients, the nitrogen monoxide generation through a microwave torch is carried out for a development of medical tool. The nitrogen monoxide concentration from a microwave plasma-torch can be easily controlled by the nitrogen flow rate, mole fraction of the oxygen gas, and the microwave power. A simple analytic expression of the nitrogen monoxide concentration is obtained in terms of the oxygen molecular density and gas flow rate. The experimental data agree remarkably well with the theoretical results from the analytical expression. A microwave nitrogen-torch can easily provide an appropriate nitrogen monoxide concentration for the wound healings.

Uhm, Han S.; Na, Young H.; Choi, Eun H.; Cho, Guangsup [Department of Electronic and Biological Physics, Kwangwoon University 447-1 Wolgye-Dong, Nowon-Gu, Seoul 137-701 (Korea, Republic of)] [Department of Electronic and Biological Physics, Kwangwoon University 447-1 Wolgye-Dong, Nowon-Gu, Seoul 137-701 (Korea, Republic of)

2013-08-15T23:59:59.000Z

248

CARBON-CARBON COMPOSITE ALLCOMP Carbon-Carbon Composite  

E-Print Network [OSTI]

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

Rollins, Andrew M.

249

Comparative study of upper critical field Hc2 and second magnetization peak Hsp in hole- and electron-doped BaFe2As2 superconductor  

Science Journals Connector (OSTI)

A comparative study of the upper critical field Hc2 and second magnetization peak Hsp was performed using high-quality single crystals of hole-doped Ba0.68K0.32Fe2As2 and electron-doped BaFe1.85Co0.15As2 and BaFe1.91Ni0.09As2. The Hc2 was extracted from both resistivity and magnetization measurements using varying magnetic fields on H?c and H?c orientations. The anisotropic ratio, ?=Hc2?c/Hc2?c, was observed to decrease to ?2.5 for the hole-doped and ?3.0 for both electron-doped samples as the magnetic fields were increased up to 9 T. It demonstrates that the anisotropic properties only show slight change by doping aliovalent ions either in or out-of the basal plane of FeAs. For the hole-doped Ba0.68K0.32Fe2As2 the Hc2 and Hsp shift toward the higher temperature and higher field regime in the temperature-normalized (T/Tc) vortex phase diagram, suggesting a stronger vortex pinning by the comparison with the electron-doped BaFe1.85Co0.15As2 and BaFe1.91Ni0.09As2. In contrast to the As-deficiency or inhomogeneous doping distribution of K, Co, and Ni, the dense pinning centers in Ba0.68K0.32Fe2As2 may be attributed to the disordered structural domains and suggested to be responsible for the intrinsic disorder and anisotropy of iron arsenides.

D. L. Sun; Y. Liu; C. T. Lin

2009-10-12T23:59:59.000Z

250

Quantification of Black Carbon and Other Pollutant Emissions from a  

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

Quantification of Black Carbon and Other Pollutant Emissions from a Quantification of Black Carbon and Other Pollutant Emissions from a Traditional and an Improved Cookstove Title Quantification of Black Carbon and Other Pollutant Emissions from a Traditional and an Improved Cookstove Publication Type Report LBNL Report Number LBNL-6062E Year of Publication 2010 Authors Kirchstetter, Thomas W., Chelsea Preble, Odelle L. Hadley, and Ashok J. Gadgil Keywords aethalometer, Berkeley Darfur Stove, black carbon, carbon monoxide, climate change, DustTrak, global warming, improved cookstoves, indoor air quality, LBNL Stove Testing Facility, particulate matter, photoacoustic absorption spectrometer, pollutant emission factor, three-stone fire Abstract Traditional methods of cooking in developing regions of the world emit pollutants that

251

Vacancies in ordered and disordered titanium monoxide: Mechanism of B1 structure stabilization  

SciTech Connect (OSTI)

The electronic structure and stability of three phases of titanium monoxide TiO{sub y} with B1 type of the basic structure have been studied. Cubic phase without structural vacancies, TiO, and two phases with structural vacancies, monoclinic Ti{sub 5}O{sub 5} and cubic disordered TiO{sub 1.0}, was treated by means of first-principles calculations within the density functional theory with pseudo-potential approach based on the plane wave's basis. The ordered monoclinic phase Ti{sub 5}O{sub 5} was found to be the most stable and the cubic TiO without vacancies the less stable one. The role of structural vacancies in the titanium sublattice is to decrease the Fermi energy, the role of vacancies in the oxygen sublattice is to contribute to the appearance of Ti–Ti bonding interactions through these vacancies and to reinforce the Ti–Ti interactions close to them. Listed effects are significantly pronounced if the vacancies in the titanium and oxygen sublattices are associated in the so called “vacancy channels” which determine the formation of vacancy ordered structure of monoclinic Ti{sub 5}O{sub 5}-type. - Graphical abstract: Changes in total DOS of titanium monoxide when going from vacancy-free TiO to TiO with disordered structural vacancies and to TiO with ordered structural vacancies. Highlights: • Ordered monoclinic Ti{sub 5}O{sub 5} is the most stable phase of titanium monoxide. • Vacancy-free TiO is the less stable phase of the titanium monoxide. • Ordering of oxygen vacancies leads to the appearance of Ti–Ti bonding interactions. • Titanium vacancies contribute significantly to the decreasing of the Fermi energy.

Kostenko, M.G. [Institute of Solid State Chemistry, The Ural Branch of the Russian Academy of Sciences, Pervomayskaya 91, Ekaterinburg 620990 (Russian Federation); Lukoyanov, A.V. [Institute of Metal Physics, The Ural Branch of the Russian Academy of Sciences, S. Kovalevskoy 18, Ekaterinburg 620990 (Russian Federation); Ural Federal University named after First President of Russia B.N. Yeltsin, Mira 19, Ekaterinburg 620002 (Russian Federation); Zhukov, V.P. [Institute of Solid State Chemistry, The Ural Branch of the Russian Academy of Sciences, Pervomayskaya 91, Ekaterinburg 620990 (Russian Federation); Rempel, A.A., E-mail: rempel@ihim.uran.ru [Institute of Solid State Chemistry, The Ural Branch of the Russian Academy of Sciences, Pervomayskaya 91, Ekaterinburg 620990 (Russian Federation); Ural Federal University named after First President of Russia B.N. Yeltsin, Mira 19, Ekaterinburg 620002 (Russian Federation)

2013-08-15T23:59:59.000Z

252

?-? Rearrangement of vinylphosphonium ligand in the coordination sphere of manganese, the crystal and molecular structure of [?5-C5H5(CO)2Mn(?2-PhHc=CHP+Ph3]Cl?  

Science Journals Connector (OSTI)

By the x-ray diffraction analysis method we established the structure of [Cp(CO)2Mn (?-PhHC=CHP+Ph3)]Cl?.

N. E. Kolobova; O. M. Khitrova…

1987-09-01T23:59:59.000Z

253

INDOOR AIR QUALITY  

E-Print Network [OSTI]

carbon monoxide, nitrogen dioxide, formaldehyde, radon, andcarbon monoxide (CO), nitrogen dioxide (N0 ), formaldehyde (

Hollowell, C.D.

2010-01-01T23:59:59.000Z

254

Carbon sequestration  

Science Journals Connector (OSTI)

...Leaver and Howard Dalton Carbon sequestration Rattan Lal * * ( lal.1...and biotic technologies. Carbon sequestration implies transfer of atmospheric...and biomass burning. 3. Carbon sequestration Emission rates from fossil...

2008-01-01T23:59:59.000Z

255

Carbon Sequestration  

Science Journals Connector (OSTI)

Carbon sequestration” refers to a portfolio of activities for ... capture, separation and storage or reuse of carbon or CO2. Carbon sequestration technologies encompass both the prevention of CO2 emissions into ...

Robert L. Kane MS; Daniel E. Klein MBA

2005-01-01T23:59:59.000Z

256

Modification of Y Zeolite with Alkaline Treatment: Textural Properties and Catalytic Activity for Diethyl Carbonate Synthesis  

Science Journals Connector (OSTI)

(1) Compared to dimethyl carbonate (DMC) and ethanol, DEC has been proposed as a potential fuel oxygenate additive to replace methyl tert-butyl ether (MTBE) because of its high oxygen content (40.6 wt %) and favorable fuel/water partition coefficient. ... For CuY using untreated zeolite as a support, there were only two H2-comsumption peaks at 473 and 681 K, ascribed to the Cu+ located on sites III? and II. ... Dunn, B. C.; Guenneau, C.; Hilton, S. A.; Pahnke, J.; Eyring, E. M.Production of diethyl carbonate from ethanol and carbon monoxide over a heterogeneous catalyst Energy Fuels 2002, 16, 177– 181 ...

Shouying Huang; Pengzhen Chen; Bing Yan; Shengping Wang; Yongli Shen; Xinbin Ma

2013-04-20T23:59:59.000Z

257

Control-oriented input-delay model of the distributed temperature of a SI engine exhaust  

E-Print Network [OSTI]

shifting [8]. This open-loop technique leads to a faster heating of the catalyst but also yields combustion the combustion: hydrocar- bons HC, carbon monoxide CO and nitrogen oxide NOx. Yet, conversion efficiency Delphine to activate chemical re- actions and the catalyst conversion ratio is poor [18]. Therefore, speed

258

2114 Znorg. Chem. 1989,28, 21 14-21 19 Contribution from the School of Chemical Sciences,  

E-Print Network [OSTI]

6*' and of carbon monoxide to methanol8 that are effected by the group 4 hydrides Cp2ZrHC1 and (C5Me) and 120.6 (1)O. Its structure differs fundamentally from that of the titanium analogue Ti(BH4)3(PMe,)2,and

Girolami, Gregory S.

259

ILYA KOLMANOVSKY, PAUL MORAAL, MICHIEL VAN NIEUWSTADT AND ANNA STEFANOPOULOU  

E-Print Network [OSTI]

components are increasingly being considered for production of passenger car internal combustion engines), oxides of nitrogen (NOx), hydrocarbons (HC) and carbon monoxide (CO). Speci - cally, increased air gas and it increases the speci c heat capacity of the charge. This reduces the burn rate, lowering

Stefanopoulou, Anna

260

THE PROBLEM OF COLD STARTS:1 A CLOSER LOOK AT MOBILE SOURCE EMISSIONS LEVELS2  

E-Print Network [OSTI]

(pre-)heated catalysts, using the bigger batteries available34 on hybrid drivetrains and plug Agency (EPA) has been regulating the light-duty vehicle fleet's hydrocarbon (HC), carbon41 monoxide (CO, when engine block and coolant temperatures are low, incomplete combustion results in44 #12

Kockelman, Kara M.

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


261

Envlron. Sci. Technol. 1993, 27, 1885-1891 On-Road Hydrocarbon Remote Sensing in the Denver Area  

E-Print Network [OSTI]

), oxides of nitrogen (NO,), and other toxic air pollutants. These emissions play important roles in all emission control technology. Introduction Automobile emissionsoriginate from fuelrich-burning, misfiring or nonfunctional emission control system can produce high emission rates for carbon monoxide (CO), hydrocarbon (HC

Denver, University of

262

Pre-Combustion Carbon Capture Research | Department of Energy  

Broader source: Energy.gov (indexed) [DOE]

Pre-Combustion Carbon Capture Research Pre-Combustion Carbon Capture Research Pre-Combustion Carbon Capture Research Pre-combustion capture refers to removing CO2 from fossil fuels before combustion is completed. For example, in gasification processes a feedstock (such as coal) is partially oxidized in steam and oxygen/air under high temperature and pressure to form synthesis gas. This synthesis gas, or syngas, is a mixture of hydrogen, carbon monoxide, CO2, and smaller amounts of other gaseous components, such as methane. The syngas can then undergo the water-gas shift reaction to convert CO and water (H2O) to H2 and CO2, producing a H2 and CO2-rich gas mixture. The concentration of CO2 in this mixture can range from 15-50%. The CO2 can then be captured and separated, transported, and ultimately sequestered, and the H2-rich fuel combusted.

263

I'hc I>ci~~t'tiiicnt-wIclc A-70 Infomiation Technology (IT) Competitive Sourcirig  

Broader source: Energy.gov (indexed) [DOE]

5 5 , 3004 SIJI3JII( ' ' 1 ~ : 1'1' A-76 'I'ransition f'lanning and Iniplcnientation I'hc I>ci~~t'tiiicnt-wIclc A-70 Infomiation Technology (IT) Competitive Sourcirig Study i s iiioving into the final phascs. AS you know, the request lor propos;il ( i < l ~ ' l ~ ) W;IS rclcasccl in mid-Aiigiist. I would lIke lo taltc this oppor-turiity lo itifbr-ni yo11 ol- liitur-c ;ictivitics rclatcti to the remaining aspects of the proccss. 'l'lic cvnipetitivc sourcing study has provided the entire Department with ;I ~iriiqtic opportunity to reaffirm it's cnininitniciit to strengthened 1'1' policics and practices. As w c move hrward, it is imperative to ilriplcmcnt various policies, plans, a i ~ l ;iclivities t-clatcd t o IT organizational realignment and thc acquisition of 1'1'

264

HC: 749 (7/14) CruzCare Enroll/Cancel Form UCSC Student Health Services Phone: (831) 459-2389 Fax: (831) 459-4050  

E-Print Network [OSTI]

HC: 749 (7/14) CruzCare Enroll/Cancel Form UCSC Student Health Services Phone: (831) 459-2389 Fax quarterly to the student's account) CruzCare provides unlimited Student Health Center visits for care-ray charges, CruzCare pays for itself with a single visit to the Student Health Center. What is covered

California at Santa Cruz, University of

265

Fluorine-Doped Carbon Blacks: Highly Efficient Metal-Free Electrocatalysts for Oxygen Reduction Reaction  

Science Journals Connector (OSTI)

As a result of the energy crisis in the world, fuel cells are attractive as clean and sustainable energy conversion devices because they can help address the ever increasing global energy demand. ... (2, 3) To date, Pt-based materials are the most widely used electrocatalysts for ORR;(4-6) however, Pt-based catalysts suffer from problems, such as sluggish oxygen reduction at any pH, durability, very limited reserves, high cost, and inactivation by carbon monoxide (CO) poisoning. ...

Xiujuan Sun; Yuwei Zhang; Ping Song; Jing Pan; Lin Zhuang; Weilin Xu; Wei Xing

2013-07-03T23:59:59.000Z

266

Carbon Smackdown: Carbon Capture  

SciTech Connect (OSTI)

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

Jeffrey Long

2010-07-12T23:59:59.000Z

267

Process for the conversion of carbonaceous feedstocks to particulate carbon and methanol  

DOE Patents [OSTI]

A process is described for the production of a pollutant-free particulate carbon (i.e., a substantially ash-, sulfur- and nitrogen-free carbon) from carbonaceous feedstocks. The basic process involves de-oxygenating one of the gas streams formed in a cyclic hydropyrolysis-methane pyrolysis process in order to improve conversion of the initial carbonaceous feedstock. De-oxygenation is effected by catalytically converting carbon monoxide, carbon dioxide, and hydrogen contained in one of the pyrolysis gas streams, preferably the latter, to a methanol co-product. There are thus produced two products whose use is known per se, viz., a substantially pollutant-free particulate carbon black and methanol. These products may be admixed in the form of a liquid slurry of carbon black in methanol. 3 figs.

Steinberg, M.; Grohse, E.W.

1995-06-27T23:59:59.000Z

268

Process for the conversion of carbonaceous feedstocks to particulate carbon and methanol  

DOE Patents [OSTI]

A process for the production of a pollutant-free particulate carbon (i.e., a substantially ash-, sulfur- and nitrogen-free carbon) from carbonaceous feedstocks. The basic process involves de-oxygenating one of the gas streams formed in a cyclic hydropyrolysis-methane pyrolysis process in order to improve conversion of the initial carbonaceous feedstock. De-oxygenation is effected by catalytically converting carbon monoxide, carbon dioxide, and hydrogen contained in one of the pyrolysis gas streams, preferably the latter, to a methanol co-product. There are thus produced two products whose use is known per se, viz., a substantially pollutant-free particulate carbon black and methanol. These products may be admixed in the form of a liquid slurry of carbon black in methanol.

Steinberg, Meyer (Melville, NY); Grohse, Edward W. (Port Jefferson, NY)

1995-01-01T23:59:59.000Z

269

ON IRON MONOXIDE NANOPARTICLES AS A CARRIER OF THE MYSTERIOUS 21 ?m EMISSION FEATURE IN POST-ASYMPTOTIC GIANT BRANCH STARS  

SciTech Connect (OSTI)

A prominent mysterious emission feature peaking at ?20.1 ?m—historically known as the '21 ?m' feature—is seen in over two dozen Galactic and Magellanic Cloud carbon-rich, post-asymptotic giant branch (post-AGB) stars. The nature of its carrier remains unknown since the first detection of the 21 ?m feature in 1989. Over a dozen materials have been suggested as possible carrier candidates. However, none of them has been accepted: they either require too much material (compared to what is available in the circumstellar shells around these post-AGB stars), or exhibit additional emission features that are not seen in these 21 ?m sources. Recently, iron monoxide (FeO) nanoparticles seem to be a promising carrier candidate as Fe is an abundant element and FeO emits exclusively at ?21 ?m. In this work, using the proto-typical protoplanetary nebula HD 56126 as a test case, we examine FeO nanoparticles as a carrier for the 21 ?m feature by modeling their infrared emission, with FeO being stochastically heated by single stellar photons. We find that FeO emits too broad a 21 ?m feature to explain that observed and the Fe abundance required to be locked up in FeO exceeds what is available in HD 56126. We therefore conclude that FeO nanoparticles are not likely to be responsible for the 21 ?m feature.

Li, Aigen; Jiang, B. W. [Department of Physics and Astronomy, University of Missouri, Columbia, MO 65211 (United States); Liu, J. M., E-mail: lia@missouri.edu, E-mail: bjiang@bnu.edu.cn [Department of Astronomy, Beijing Normal University, Beijing 100875 (China)

2013-11-10T23:59:59.000Z

270

Carbon Conference  

Science Journals Connector (OSTI)

Carbon Conference ... The Fourth Hienninl Conference on Carbon will be held at the University of Buffalo, June 15 to 19. ... The Pittsburgh Section's coal technology group will meet in the conference room at Mellon Institute, Pittsburgh, June ... ...

1959-06-01T23:59:59.000Z

271

Multi-phase Multi-dimensional Analysis of PEM Fuel Cells with Carbon Monoxide Poisoning and Oxygen Bleeding.  

E-Print Network [OSTI]

??Polymer electrolyte membrane (PEM) fuel cells are promising alternative green power source for mobile, portable and stationary applications. However, their cost, durability, and performance are… (more)

Li, Yaqun

2010-01-01T23:59:59.000Z

272

Daily and 3-hourly variability in global fire emissions and consequences for atmospheric model predictions of carbon monoxide  

E-Print Network [OSTI]

of biomass burning in South?America, Int. J. Remote Sens. ,D24303 fire season in South America, J. Geophys. Res. , 103(across North, South and Central America, Remote Sens.

2011-01-01T23:59:59.000Z

273

REDUCTION OF NITRIC OXIDE BY CARBON MONOXIDE OVER A SILICA SUPPORTED PLATINUM CATALYST: INFRARED AND KINETIC STUDIES  

E-Print Network [OSTI]

System. • B. Procedures. Catalyst Preparation Infrared DiskPreparation. Catalyst Characterization. PreliminaryReduction by CO Over a Pt Catalyst," M.S. thesis, Department

Lorimer, D.H.

2011-01-01T23:59:59.000Z

274

Thermodesorption studies of catalytic systems. 16. The carbon monoxide-water vapor conversion on copper-containing catalysts  

SciTech Connect (OSTI)

Thermodesorption studies have shown the presence of several types of centers: centers for the firm irreversible adsorption of CO, centers for the adsorption of H/sub 2/O, centers for the competitive adsorption of CO and H/sub 2/O, and centers for the CO-H/sub 2/O conversion, on the surface of the skeletal copper catalyst. It is suggested that CO adsorbs in bridged form on the competitive adsorption centers, and in linear form on the reaction centers. The conversion reaction involves CO and H/sub 2/O molecules adsorbed on a small fraction (approx. 1%) of centers, the H/sub 2/O molecules in question being in the associative adsorbed form.

Gel'man, V.N.; Varlamova, A.M.; Sobolevskii, V.S.; Golosman, E.Z.; Yakerson, V.I.

1981-03-01T23:59:59.000Z

275

An infrared spectroscopy study of carbon monoxide adsorption on. alpha. -chromia surfaces: Probing oxidation states of coordinatively unsaturated surface cations  

SciTech Connect (OSTI)

CO adsorption on thermoevacuated, H{sub 2}-reduced and O{sub 2}-treated {alpha}-chromia surfaces was studied by IR spectroscopy in the temperature range 77-298 K. Coordinatively unsaturated (cus) Cr{sup 3+} cation sites, probably in 3-coordinate and to a much lesser extent 5-coordinate states, are the adsorption sites on H{sub 2}-reduced {alpha}-Cr{sub 2}O{sub 3}. The surface containing excess oxygen also exposes cus Cr{sup 4+} and Cr{sup 5+} sites. An empirical procedure is described which permits the determination of oxidation state and coordination number of the cus surface sites. This procedure is based on a correlation between C-O stretching frequency and electric field strength exerted by the cation. The latter is calculated from Pauling's strength of the electrostatic bond and effective ionic radii, both of which take the cation coordination into account.

Zaki, M.I.; Knoezinger, H. (Universitaet Muenchen (West Germany))

1989-10-01T23:59:59.000Z

276

Catalytic oxidation of carbon monoxide over Ir/SiO/sub 2/. An in situ infrared and kinetic study  

SciTech Connect (OSTI)

The oxidation of CO on a highly dispersed Ir/SiO/sub 2/ catalyst has been studied both in a Pyrex microreactor and by using an in situ infrared cell-reactor. Multiple steady states obtained under conditions of increasing and decreasing CO partial pressure were observed to lead to reaction rate hysteresis. The area under the hysteresis loop is strongly dependent on reaction temperature. This is explained by invoking competitive adsorption between CO and O/sub 2/ as a function of temperature. Self-sustained oscillations were obtained when certain conditions of partial pressure and temperature were met. Quantitative estimates of fluctuations in surface coverage and temperature during these oscillations were 10% and 3K, respectively. CO islands of reactivity were not observed under the conditions of this study. The presence of higher oxidation states of IR could not be unequivocally determined by using infrared spectroscopy. 29 references, 8 figures, 2 tables.

Saymeh, R.A.; Gonzalez, R.D.

1986-02-13T23:59:59.000Z

277

The isotopic record of Northern Hemisphere atmospheric carbon monoxide1 since 1950; implications for the CO budget Supplementary Material2  

E-Print Network [OSTI]

), the mass balance calculation can be performed with the following equation:54 13 C= i=1 7 [COi ]/[CO]Ã? 13

Meskhidze, Nicholas

278

Spectroscopic study of a Cu/CeO{sub 2} catalyst subjected to redox treatments in carbon monoxide and oxygen  

SciTech Connect (OSTI)

Redox processes induced by interaction of a calcined Cu/CeO{sub 2} catalyst with CO and reoxidation with O{sub 2} have been investigated by CO-TPR, EPR, FTIR of adsorbed CO, and XPS. The initial calcined samples shows the presence of dispersed Cu{sup 2+} species, which give rise in the EPR spectrum to signals due to isolated entities, a somewhat more aggregated Cu{sup 2+}-containing phase, and copper ionic pairs, in coexistence with an EPR-silent CuO-type phase, revealed by XPS. A significant reduction of copper is produced already by contact with CO at room temperature, EPR results suggesting that reducibility of Cu{sup 2+} species decreases with their aggregation degree. Simultaneously, the ceria surface is also reduced by this interaction, copper acting as a strong promoter of this process. A singular consequence of the synergistic reduction of both components is observed by subjecting the catalyst to CO at T{sub r} {ge} 473 K, at which the CO adsorption capability of copper is apparently suppressed, in view of the absence of copper carbonyls in the FTIR spectrum. This is attributed to the establishment of electronic interactions between reduced ceria and small metallic copper particles generated by the reduction process. Contact of the CO-reduced sample with O{sub 2} at room or higher temperature produces an important reoxidation of both copper and ceria, revealed by FTIR and EPR. The synergetic effects between copper and ceria in the reduction process and the easy reoxidation of deeply reduced ceria are thought to be crucial to explaining the high catalytic activity shown by this system for CO oxidation.

Martinez-Arias, A.; Fernandez-Garcia, M.; Soria, J.; Conesa, J.C. [CSIC, Madrid (Spain). Instituto de Catalisis y Petroleoquimica] [CSIC, Madrid (Spain). Instituto de Catalisis y Petroleoquimica

1999-03-10T23:59:59.000Z

279

Seasonal variation of carbon monoxide in northern Japan: Fourier transform IR measurements and source-labeled model calculations  

E-Print Network [OSTI]

doi:10.1029/2002JD003093. Stricker, N. C. M. , A. Hahne, D.satellite measurements [ Stricker et al . , 1995] are shown

2006-01-01T23:59:59.000Z

280

Seasonal variation of carbon monoxide in northern Japan: Fourier transform IR measurements and source-labeled model calculations  

E-Print Network [OSTI]

emissions, fossil and bio- fuel burning and biomass burningof contributions from fossil and bio- fuel burning (FF) and

2006-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "hc carbon monoxide" 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

Broadband carbon monoxide laser system operating in the wavelength range of 2.5 - 8.3 {mu}m  

SciTech Connect (OSTI)

A two-cascade frequency conversion of CO-laser radiation is demonstrated in a single sample of a nonlinear ZnGeP{sub 2} crystal. The crystal is pumped by a repetitively pulsed cryogenic lowpressure CO laser operating on {approx}150 vibration - rotational transitions in the wavelength range 5.0 - 7.5 {mu}m, which corresponds to the frequency range of a half octave. In the first conversion cascade, generation of second harmonic and sum frequencies of various pairs of CO-laser radiation give {approx}350 emission lines in the wavelength range 2.5 - 3.7 {mu}m. In the second cascade, by mixing the radiation converted in the first cascade with the residual radiation of the CO laser we have obtained {approx}90 lines in the range 4.3 - 5.0 {mu}m and more than 80 lines in the range 7.5 - 8.3 {mu}m. Thus, using a single sample of the nonlinear ZnGeP{sub 2} crystal pumped by the radiation of a single CO laser we have produced a source of broadband (more than one and a half octaves) laser radiation, simultaneously operating at {approx}670 lines in the wavelength range 2.5 - 8.3 {mu}m. (lasers)

Andreev, Yu M; Ionin, Andrei A; Kinyaevsky, I O; Klimachev, Yu M; Kozlov, A Yu; Kotkov, A A; Lanskii, G V; Shaiduko, A V

2013-02-28T23:59:59.000Z

282

Isolation of carbon monoxide dehydrogenase from Acetobacterium woodii and comparison of its properties with those of the Clostridium thermoaceticum enzyme.  

Science Journals Connector (OSTI)

...to be the primary natural electron carrier...to be the primary natural electron carrier...to be the primary natural electron carrier...Chemical Co., Inc., Corpus Christi, Tex.). A. woodii...H2-CO2 (66/33) gas mixture or on fructose...

S W Ragsdale; L G Ljungdahl; D V DerVartanian

1983-09-01T23:59:59.000Z

283

Analysis of mid-tropospheric carbon monoxide data using a three- dimensional Global atmospheric Chemistry numerical Model  

SciTech Connect (OSTI)

The GChM atmospheric chemistry and transport model has been used to analyze the mid-tropospheric CO dataset obtained from NASA`s Measurement of Air Pollution by Satellites (MAPS) program. Fourteen simulations with a 3.75 horizontal resolution have been performed, including a base case and 13 sensitivity runs. The model reproduces many, but not all, of the major features of the MAPS dataset. Locations of peak CO mixing ratios associated with biomass burning as observed in the MAPS experiment are slightly farther south than the model result, indicating either greater horizontal transport than present in the model representation or a spatial difference between the location of modeled biomass fires and actual fires. The current version of GChM was shown to be relatively insensitive to the magnitude of the prescribed NO{sub x} and O{sub 3} global distributions and very insensitive to the depth of the mixed layer as parameterized in the model. Cloud convective transport was shown to play an important role in venting boundary layer CO to the free troposphere. This result agrees with prior meteorological analyses of the MAPS dataset that have-indirectly inferred the presence of convective activity through satellite-based information. Work is continuing to analyze the results of these simulations further and to perform more detailed comparisons between model results and MAPS data.

Easter, R.C.; Saylor, R.D.; Chapman, E.G.

1993-12-01T23:59:59.000Z

284

GALLIUM NITRIDE INTEGRATED GAS/TEMPERATURE SENSORS FOR FUEL CELL SYSTEM MONITORING FOR HYDROGEN AND CARBON MONOXIDE  

E-Print Network [OSTI]

on field effect devices using catalytic metal gates on silicon carbide substrates has been reviewed (Spetz-10%) of transition metals such as copper, silver, and chromium (Feinstein et al 1997 and Pyke 1993). High temperature. Introduction Gas sensing and analysis based on gas adsorption on a catalytic metal surface has been extensively

285

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

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

CDIAC products are indexed and searchable through a customized interface powered by ORNL's Mercury search engine. Products include numeric data packages, publications, trend data, atlases, 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.

286

Carbon Cycle  

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

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

287

Carbon Isotopes  

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

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

288

Observation of $e^+e^-\\to ?^0?^0 h_c$ and a neutral charmoniumlike structure $Z_c(4020)^0$  

E-Print Network [OSTI]

Using data collected with the BESIII detector operating at the Beijing Electron Positron Collider at center-of-mass energies of $\\sqrt{s}$=4.23, 4.26, and 4.36 GeV, we observe $e^+e^-\\to \\pi^0\\pi^0 h_c$ for the first time. The Born cross sections are measured and found to be about half of those of $e^+e^- \\to \\pi^+\\pi^-h_c$ within less than 2$\\sigma$. In the $\\pi^0h_c$ mass spectrum, a structure at 4.02~GeV/$c^2$ that is most likely the neutral isospin partner of the $Z_c(4020)^{\\pm}$ observed in the process of $e^+e^- \\to \\pi^+\\pi^-h_c$ is found. A fit to the $\\pi^0 h_c$ invariant mass spectrum with the width of the $Z_c(4020)^0$ fixed to that of its charged isospin partner and possible interferences with non-$Z_c(4020)^0$ amplitudes neglected, gives a mass of ($4023.9\\pm 2.2 \\pm 3.8$)~MeV/$c^2$ for the $Z_c(4020)^0$, where the first error is statistical and the second systematic.

M. Ablikim; M. N. Achasov; X. C. Ai; O. Albayrak; M. Albrecht; D. J. Ambrose; A. Amoroso; F. F. An; Q. An; J. Z. Bai; R. Baldini Ferroli; Y. Ban; D. W. Bennett; J. V. Bennett; M. Bertani; D. Bettoni; J. M. Bian; F. Bianchi; E. Boger; O. Bondarenko; I. Boyko; R. A. Briere; H. Cai; X. Cai; O. Cakir; A. Calcaterra; G. F. Cao; S. A. Cetin; J. F. Chang; G. Chelkov; G. Chen; H. S. Chen; H. Y. Chen; J. C. Chen; M. L. Chen; S. J. Chen; X. Chen; X. R. Chen; Y. B. Chen; H. P. Cheng; X. K. Chu; Y. P. Chu; G. Cibinetto; D. Cronin-Hennessy; H. L. Dai; J. P. Dai; D. Dedovich; Z. Y. Deng; A. Denig; I. Denysenko; M. Destefanis; F. De Mori; Y. Ding; C. Dong; J. Dong; L. Y. Dong; M. Y. Dong; S. X. Du; P. F. Duan; J. Z. Fan; J. Fang; S. S. Fang; X. Fang; Y. Fang; L. Fava; F. Feldbauer; G. Felici; C. Q. Feng; E. Fioravanti; C. D. Fu; Q. Gao; Y. Gao; I. Garzia; K. Goetzen; W. X. Gong; W. Gradl; M. Greco; M. H. Gu; Y. T. Gu; Y. H. Guan; A. Q. Guo; L. B. Guo; T. Guo; Y. Guo; Y. P. Guo; Z. Haddadi; A. Hafner; S. Han; Y. L. Han; F. A. Harris; K. L. He; Z. Y. He; T. Held; Y. K. Heng; Z. L. Hou; C. Hu; H. M. Hu; J. F. Hu; T. Hu; Y. Hu; G. M. Huang; G. S. Huang; H. P. Huang; J. S. Huang; X. T. Huang; Y. Huang; T. Hussain; Q. Ji; Q. P. Ji; X. B. Ji; X. L. Ji; L. L. Jiang; L. W. Jiang; X. S. Jiang; J. B. Jiao; Z. Jiao; D. P. Jin; S. Jin; T. Johansson; A. Julin; N. Kalantar-Nayestanaki; X. L. Kang; X. S. Kang; M. Kavatsyuk; B. C. Ke; R. Kliemt; B. Kloss; O. B. Kolcu; B. Kopf; M. Kornicer; W. Kuehn; A. Kupsc; W. Lai; J. S. Lange; M. Lara; P. Larin; M. Leyhe; Cheng Li; D. M. Li; F. Li; G. Li; H. B. Li; J. C. Li; Jin Li; K. Li; K. Li; Q. J. Li; T. Li; W. D. Li; W. G. Li; X. L. Li; X. M. Li; X. N. Li; X. Q. Li; Z. B. Li; H. Liang; Y. F. Liang; Y. T. Liang; G. R. Liao; D. X. Lin; B. J. Liu; C. L. Liu; C. X. Liu; F. H. Liu; Fang Liu; Feng Liu; H. B. Liu; H. H. Liu; H. H. Liu; H. M. Liu; J. Liu; J. P. Liu; J. Y. Liu; K. Liu; K. Y. Liu; L. D. Liu; Q. Liu; S. B. Liu; X. Liu; X. X. Liu; Y. B. Liu; Z. A. Liu; Zhiqiang Liu; Zhiqing Liu; H. Loehner; X. C. Lou; H. J. Lu; J. G. Lu; R. Q. Lu; Y. Lu; Y. P. Lu; C. L. Luo; M. X. Luo; T. Luo; X. L. Luo; M. Lv; X. R. Lyu; F. C. Ma; H. L. Ma; Q. M. Ma; S. Ma; T. Ma; X. N. Ma; X. Y. Ma; F. E. Maas; M. Maggiora; Q. A. Malik; Y. J. Mao; Z. P. Mao; S. Marcello; J. G. Messchendorp; J. Min; T. J. Min; R. E. Mitchell; X. H. Mo; Y. J. Mo; H. Moeini; C. Morales Morales; K. Moriya; N. Yu. Muchnoi; H. Muramatsu; Y. Nefedov; F. Nerling; I. B. Nikolaev; Z. Ning; S. Nisar; S. L. Niu; X. Y. Niu; S. L. Olsen; Q. Ouyang; S. Pacetti; P. Patteri; M. Pelizaeus; H. P. Peng; K. Peters; J. L. Ping; R. G. Ping; R. Poling; Y. N. Pu; M. Qi; S. Qian; C. F. Qiao; L. Q. Qin; N. Qin; X. S. Qin; Y. Qin; Z. H. Qin; J. F. Qiu; K. H. Rashid; C. F. Redmer; H. L. Ren; M. Ripka; G. Rong; X. D. Ruan; V. Santoro; A. Sarantsev; M. Savrié; K. Schoenning; S. Schumann; W. Shan; M. Shao; C. P. Shen; P. X. Shen; X. Y. Shen; H. Y. Sheng; M. R. Shepherd; W. M. Song; X. Y. Song; S. Sosio; S. Spataro; B. Spruck; G. X. Sun; J. F. Sun; S. S. Sun; Y. J. Sun; Y. Z. Sun; Z. J. Sun; C. J. Tang; X. Tang; I. Tapan; E. H. Thorndike; M. Tiemens; D. Toth; M. Ullrich; I. Uman; G. S. Varner; B. Wang; B. L. Wang; D. Wang; D. Y. Wang; K. Wang; L. L. Wang; L. S. Wang; M. Wang; P. Wang; P. L. Wang; Q. J. Wang; S. G. Wang; W. Wang; X. F. Wang; Y. F. Wang; Y. Q. Wang; Z. Wang; Z. G. Wang; Z. H. Wang; Z. Y. Wang; D. H. Wei; J. B. Wei; P. Weidenkaff; S. P. Wen; U. Wiedner; M. Wolke; L. H. Wu; Z. Wu; L. G. Xia; Y. Xia; D. Xiao; Z. J. Xiao; Y. G. Xie; Q. L. Xiu; G. F. Xu; L. Xu; Q. J. Xu; Q. N. Xu; X. P. Xu; Z. Xue; L. Yan; W. B. Yan; W. C. Yan; Y. H. Yan; H. X. Yang; L. Yang; Y. Yang; Y. X. Yang; H. Ye; M. Ye; M. H. Ye; J. H. Yin; B. X. Yu; C. X. Yu; H. W. Yu; J. S. Yu; C. Z. Yuan; W. L. Yuan; Y. Yuan; A. Yuncu; A. A. Zafar; A. Zallo; Y. Zeng; B. X. Zhang; B. Y. Zhang; C. Zhang; C. C. Zhang; D. H. Zhang; H. H. Zhang; H. T. Zhang; H. Y. Zhang; J. J. Zhang; J. L. Zhang; J. Q. Zhang; J. W. Zhang; J. Y. Zhang; J. Z. Zhang; K. Zhang; L. Zhang; S. H. Zhang; X. J. Zhang; X. Y. Zhang; Y. Zhang; Y. H. Zhang; Z. H. Zhang; Z. P. Zhang; Z. Y. Zhang; G. Zhao; J. W. Zhao; J. Y. Zhao; J. Z. Zhao; Lei Zhao; Ling Zhao; M. G. Zhao; Q. Zhao; Q. W. Zhao; S. J. Zhao; T. C. Zhao; Y. B. Zhao; Z. G. Zhao; A. Zhemchugov; B. Zheng; J. P. Zheng; Y. H. Zheng; B. Zhong; L. Zhou; Li Zhou; X. Zhou; X. K. Zhou; X. R. Zhou; X. Y. Zhou; K. Zhu; K. J. Zhu; S. Zhu; X. L. Zhu; Y. C. Zhu; Y. S. Zhu; Z. A. Zhu; J. Zhuang; B. S. Zou; J. H. Zou

2014-09-23T23:59:59.000Z

289

Integration of carbonate fuel cells with advanced coal gasification systems  

SciTech Connect (OSTI)

Carbonate fuel cells have attributes which make them ideally suited to operate on coal-derived fuel gas; they can convert the methane, hydrogen, and carbon monoxide present in coal derived fuel gas directly to electricity, are not subject to thermodynamic cycle limits as are heat engines, and operate at temperatures compatible with coal gasifiers. Some new opportunities for improved efficiency have been identified in integrated coal gasification/carbonate fuel cells which take advantage of low temperature catalytic coal gasification producing a methane-rich fuel gas, and the internal methane reforming capabilities of Energy Research Corporation`s carbonate fuel cells. By selecting the appropriate operating conditions and catalyst in the gasifier, methane formation is maximized to improve gasification efficiency and to take advantage of the heat management aspects of the internal reforming carbonate fuel cell. These advanced integrated gasification/carbonate fuel cell systems are projected to have better efficiencies than gasification/carbonate fuel cell systems employing conventional gasification, and also competing non-fuel cell systems. These improved efficiencies would be accompanied by a corresponding reduction in impact on the environment as well.

Steinfeld, G. [Energy Research Corp., Danbury, CT (United States); Meyers, S.J. [Fluor Daniel, Inc., Irvine, CA (United States); Hauserman, W.B. [North Dakota Univ., Grand Forks, ND (United States). Energy and Environmental Research Center

1992-12-01T23:59:59.000Z

290

Integration of carbonate fuel cells with advanced coal gasification systems  

SciTech Connect (OSTI)

Carbonate fuel cells have attributes which make them ideally suited to operate on coal-derived fuel gas; they can convert the methane, hydrogen, and carbon monoxide present in coal derived fuel gas directly to electricity, are not subject to thermodynamic cycle limits as are heat engines, and operate at temperatures compatible with coal gasifiers. Some new opportunities for improved efficiency have been identified in integrated coal gasification/carbonate fuel cells which take advantage of low temperature catalytic coal gasification producing a methane-rich fuel gas, and the internal methane reforming capabilities of Energy Research Corporation's carbonate fuel cells. By selecting the appropriate operating conditions and catalyst in the gasifier, methane formation is maximized to improve gasification efficiency and to take advantage of the heat management aspects of the internal reforming carbonate fuel cell. These advanced integrated gasification/carbonate fuel cell systems are projected to have better efficiencies than gasification/carbonate fuel cell systems employing conventional gasification, and also competing non-fuel cell systems. These improved efficiencies would be accompanied by a corresponding reduction in impact on the environment as well.

Steinfeld, G. (Energy Research Corp., Danbury, CT (United States)); Meyers, S.J. (Fluor Daniel, Inc., Irvine, CA (United States)); Hauserman, W.B. (North Dakota Univ., Grand Forks, ND (United States). Energy and Environmental Research Center)

1992-01-01T23:59:59.000Z

291

MOBILE6 Vehicle Emission Modeling Software | Open Energy Information  

Open Energy Info (EERE)

MOBILE6 Vehicle Emission Modeling Software MOBILE6 Vehicle Emission Modeling Software Jump to: navigation, search Tool Summary Name: MOBILE6 Agency/Company /Organization: United States Environmental Protection Agency Sector: Energy Focus Area: Transportation Topics: GHG inventory Resource Type: Software/modeling tools User Interface: Desktop Application Website: www.epa.gov/oms/m6.htm Cost: Free References: http://www.epa.gov/oms/m6.htm MOBILE6 is an emission factor model for predicting gram per mile emissions of Hydrocarbons (HC), Carbon Monoxide (CO), Nitrogen Oxides (NOx), Carbon Dioxide (CO2), Particulate Matter (PM), and toxics from cars, trucks, and motorcycles under various conditions. MOBILE6 is an emission factor model for predicting gram per mile emissions of Hydrocarbons (HC), Carbon Monoxide (CO), Nitrogen Oxides (NOx), Carbon

292

Synthesis and characterization of lignin-based carbon materials with tunable microstructure  

SciTech Connect (OSTI)

Lignin-based carbons can be used as a low-cost alternative to graphite and petroleum-based carbons enabling the production of sustainable, functional carbon materials for various applications. The microstructure development of these carbons can be controlled through chemical modification of the lignin precursor and choice of carbonization parameters. In this work, microstructured carbon materials are synthesized from lignin using a combination of chemical modification and carbon fiber processing techniques. Lignin is modified by incorporating different ester groups which results in a precursor highly compatible with melt processing using the fiber extrusion technique and conversion into microstructured carbons by oxidative stabilization and subsequent carbonization. Furthermore, the impact of esterifications on precursor chemistry and carbonizations is investigated. A nuclear magnetic resonance study of modified lignins shows characteristic spectral changes as a result of esterifications. Ultrahigh resolution Fourier transform ion cyclotron resonance mass spectrometry shows the modification process does not affect the polymeric character of the lignin backbone. Esterifications result in moderate shifts in O:C and H:C ratios. Thermogravimetric analysis of lignins reveals distinct differences in mass loss trends during oxidations and carbonizations.

Chatterjee, Sabornie [ORNL] [ORNL; Clingenpeel, Amy [National High Magnetic Field Laboratory (Magnet Lab), Florida] [National High Magnetic Field Laboratory (Magnet Lab), Florida; McKenna, Amy [National High Magnetic Field Laboratory (Magnet Lab), Florida] [National High Magnetic Field Laboratory (Magnet Lab), Florida; Rios, Orlando [ORNL] [ORNL; Johs, Alexander [ORNL] [ORNL

2013-01-01T23:59:59.000Z

293

Carbon Nanotubes.  

E-Print Network [OSTI]

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

Fredriksson, Tore

2014-01-01T23:59:59.000Z

294

Capturing carbon | EMSL  

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

Capturing carbon Capturing carbon New technology enables molecular-level insight into carbon sequestration Carbon sequestration is a potential solution for reducing greenhouse...

295

Carbon dioxide adsorption and methanation on ruthenium  

SciTech Connect (OSTI)

The adsorption and methanation of carbon dioxide on a ruthenium-silica catalyst were studied using temperature-programmed desorption (TPD) and temperature-programmed reaction (TPR). Carbon dioxide adsorption was found to be activated; CO/sub 2/ adsorption increased significantly as the temperature increased from 298 to 435 K. During adsorption, some of the CO/sub 2/ dissociated to carbon monoxide and oxygen; upon hydrogen exposure at room temperature, the oxygen reacted to water. Methanation of adsorbed CO and of adsorbed CO/sub 2/, using TPR in flowing hydrogen, yielded a CH/sub 4/ peak with a peak temperature of 459 K for both adsorbates, indicating that both reactions follow the same mechanism after adsorption. This peak temperature did not change with initial surface coverage of CO, indicating that methanation is first order in CO coverage. The desorption and reaction spectra for Ru/SiO/sub 2/ were similar to those previously obtained for Ni/SiO/sub 2/, but both CO/sub 2/ formation and CH/sub 4/ formation proceeded faster on Ru. Also, the details of CO desorption and the changes in CO/sub 2/ and CO desorptions with initial coverage were different on the two metals. 5 figures, 3 tables.

Zagli, E.; Falconer, J.L.

1981-05-01T23:59:59.000Z

296

A digital map of the high center (HC) and low center (LC) polygon boundaries delineated from high resolution LiDAR data for Barrow, Alaska  

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

This dataset represent a map of the high center (HC) and low center (LC) polygon boundaries delineated from high resolution LiDAR data for the arctic coastal plain at Barrow, Alaska. The polygon troughs are considered as the surface expression of the ice-wedges. The troughs are in lower elevations than the interior polygon. The trough widths were initially identified from LiDAR data, and the boundary between two polygons assumed to be located along the lowest elevations on trough widths between them.

Gangodagamage, Chandana; Wullschleger, Stan

297

A digital map of the high center (HC) and low center (LC) polygon boundaries delineated from high resolution LiDAR data for Barrow, Alaska  

SciTech Connect (OSTI)

This dataset represent a map of the high center (HC) and low center (LC) polygon boundaries delineated from high resolution LiDAR data for the arctic coastal plain at Barrow, Alaska. The polygon troughs are considered as the surface expression of the ice-wedges. The troughs are in lower elevations than the interior polygon. The trough widths were initially identified from LiDAR data, and the boundary between two polygons assumed to be located along the lowest elevations on trough widths between them.

Gangodagamage, Chandana; Wullschleger, Stan

2014-07-03T23:59:59.000Z

298

Carbon Sequestration  

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

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

299

Carbon Nanotubes  

Science Journals Connector (OSTI)

A broad review of the structure and properties of carbon nanotubes is presented. Particular emphasis is given to ... dimensional density of states predicted for single-wall nanotubes of small diameter. The eviden...

M. S. Dresselhaus; G. Dresselhaus…

2000-01-01T23:59:59.000Z

300

Carbon Fiber  

ScienceCinema (OSTI)

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

McGetrick, Lee

2014-07-23T23:59:59.000Z

Note: This page contains sample records for the topic "hc carbon monoxide" 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

Carbon Fiber  

SciTech Connect (OSTI)

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

McGetrick, Lee

2014-04-17T23:59:59.000Z

302

Growth direction of oblique angle electron beam deposited silicon monoxide thin films identified by optical second-harmonic generation  

SciTech Connect (OSTI)

Oblique angle deposited (OAD) silicon monoxide (SiO) thin films forming tilted columnar structures have been characterized by second-harmonic generation. It was found that OAD SiO leads to a rotationally anisotropic second-harmonic response, depending on the optical angle of incidence. A model for the observed dependence of the second-harmonic signal on optical angle of incidence allows extraction of the growth direction of OAD films. The optically determined growth directions show convincing agreement with cross-sectional scanning electron microscopy images. In addition to a powerful characterization tool, these results demonstrate the possibilities for designing nonlinear optical devices through SiO OAD.

Vejling Andersen, Søren; Lund Trolle, Mads; Pedersen, Kjeld [Department of Physics and Nanotechnology, Aalborg University, Skjernvej 4A, DK-9220 Aalborg Øst (Denmark)] [Department of Physics and Nanotechnology, Aalborg University, Skjernvej 4A, DK-9220 Aalborg Øst (Denmark)

2013-12-02T23:59:59.000Z

303

Low Carbon Fuel Standards  

E-Print Network [OSTI]

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

Sperling, Dan; Yeh, Sonia

2009-01-01T23:59:59.000Z

304

Delayed carbon sequestration and rising carbon prices  

Science Journals Connector (OSTI)

We set out a dynamic model to investigate optimal time paths of emissions, carbon stocks and carbon sequestration by land conversion, allowing for non-instantaneous carbon sequestration. Previous research in a dy...

Alejandro Caparrós

2009-10-01T23:59:59.000Z

305

Carbon Additionality: Discussion Paper  

E-Print Network [OSTI]

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

306

Reducing Emissions of Persistent Organic Pollutants from a Diesel Engine by Fueling with Water-Containing Butanol Diesel Blends  

Science Journals Connector (OSTI)

An increasing energy demand and environmental pollution has motivated a search for bio-fuels, such as bio-diesels(1, 2) and bio-alcohols,(3, 4) that can be used as alternative fuels for diesel engines. ... In general, both bio-diesel and bio-alcohols, such as ethanol and butanol, have the advantages of higher brake thermal efficiency (BTE) and lower emissions of particulate matter (PM), carbon monoxide (CO) and hydrocarbons (HC). ... Diesel Engine and Test Cycle ...

Yu-Cheng Chang; Wen-Jhy Lee; Hsi-Hsien Yang; Lin-Chi Wang; Jau-Huai Lu; Ying I. Tsai; Man-Ting Cheng; Li-Hao Young; Chia-Jui Chiang

2014-04-16T23:59:59.000Z

307

Carbon Sequestration  

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

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

308

Carbon Sequestration  

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

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

309

Deshpande, B., H.C. Frey, Y. Cao, and Z. Liu, "Modeling of the Penetration of Ambient PM2.5 to Indoor Residential Microenvironment," Paper 2009-A-86-AWMA, Proceedings, 102nd Annual Conference and Exhibition, Air & Waste  

E-Print Network [OSTI]

-PM residential indoor model indicates that air exchange rate, deposition rate and penetration factor affectDeshpande, B., H.C. Frey, Y. Cao, and Z. Liu, "Modeling of the Penetration of Ambient PM2 of the Penetration of Ambient PM2.5 to Indoor Residential Microenvironment Paper: 2009-A-86-AWMA Bela K. Deshpande, H

Frey, H. Christopher

310

H.C. DORLAND, N.J. BEUKES, J. GUTZMER, D.A.D. EVANS AND R.A. ARMSTRONG SOUTH AFRICAN JOURNAL OF GEOLOGY, 2006, VOLUME 109 PAGE 139-156  

E-Print Network [OSTI]

H.C. DORLAND, N.J. BEUKES, J. GUTZMER, D.A.D. EVANS AND R.A. ARMSTRONG SOUTH AFRICAN JOURNAL.evans@yale.edu R.A. Armstrong Research School of Earth Sciences, Australian National University, Canberra, Australia e-mail: Richard.Armstrong@anu.edu.au © 2006 March Geological Society of South Africa ABSTRACT

311

Frey, H.C., and P.Y. Kuo, "Potential Best Practices for Reducing Greenhouse Gas (GHG) Emissions in Freight Transportation," Paper No. 2007-AWMA-443, Proceedings, 100th  

E-Print Network [OSTI]

Frey, H.C., and P.Y. Kuo, "Potential Best Practices for Reducing Greenhouse Gas (GHG) Emissions Gas (GHG) Emissions in Freight Transportation Extended Abstract # 2007-A-443-AWMA H. Christopher Frey for approximately 9% of total greenhouse gas (GHG) emissions in the United States.1-2 The individual contributions

Frey, H. Christopher

312

Hanna, A., J. Vukovich, S. Arunachalam, D. Loughlin, H.C. Frey, J. Touma, J. Irwin, and V. Isakov, "Assessment of Uncertainty in Benzene Concentration Estimates in the Houston, TX, Area," Proceedings, Annual Meeting of the Air &  

E-Print Network [OSTI]

Hanna, A., J. Vukovich, S. Arunachalam, D. Loughlin, H.C. Frey, J. Touma, J. Irwin, and V. Isakov Carolina Environmental Program University of North Carolina at Chapel Hill H. Christopher Frey North Carolina State University Jawad Touma and John Irwin U. S. Environmental Protection Agency Vlad Isakov

Frey, H. Christopher

313

Carbon Trading, Carbon Taxes and Social Discounting  

E-Print Network [OSTI]

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

Weiblen, George D

314

Characteristics of carbonized sludge for co-combustion in pulverized coal power plants  

SciTech Connect (OSTI)

Co-combustion of sewage sludge can destabilize its combustion profile due to high volatility, which results in unstable flame. We carried out fuel reforming for sewage sludge by way of carbonization at pyrolysis temperature of 300-500 deg. C. Fuel characteristics of carbonized sludge at each temperature were analyzed. As carbonization temperature increased, fuel ratio increased, volatile content reduced, and atomic ratio relation of H/C and O/C was similar to that of lignite. The analysis result of FT-IR showed the decrease of aliphatic C-H bond and O-C bond in carbonization. In the analysis result of TG-DTG, the thermogravimetry reduction temperature of carbonized sludge (CS400) was proven to be higher than that of dried sludge, but lower than that of sub-bituminous coal. Hardgrove grindability index increased in proportion to fuel ratio increase, where the carbonized sludge value of 43-110 was similar or higher than the coal value of 49-63. As for ash deposits, slagging and fouling index were higher than that of coal. When carbonized sludge (CS400) and coal were co-combusted in 1-10% according to calorific value, slagging tendency was low in all conditions, and fouling tendency was medium or high according to the compositions of coal.

Park, Sang-Woo [Department of Environmental Engineering, Hanbat National University, Daejeon 305-719 (Korea, Republic of); Jang, Cheol-Hyeon, E-mail: jangch@hanbat.ac.kr [Department of Environmental Engineering, Hanbat National University, Daejeon 305-719 (Korea, Republic of)

2011-03-15T23:59:59.000Z

315

Gasification behavior of carbon residue in bed solids of black liquor gasifier  

SciTech Connect (OSTI)

Steam gasification of carbon residue in bed solids of a low-temperature black liquor gasifier was studied using a thermogravimetric system at 3 bar. Complete gasification of the carbon residue, which remained unreactive at 600 C, was achieved in about 10 min as the temperature increased to 800 C. The rate of gasification and its temperature dependence were evaluated from the non-isothermal experiment results. Effects of particle size and adding H{sub 2} and CO to the gasification agent were also studied. The rate of steam gasification could be taken as zero order in carbon until 80% of carbon was gasified, and for the rest of the gasification process the rate appeared to be first order in carbon. The maximum rate of carbon conversion was around 0.003/s and the activation energy was estimated to be in the range of 230-300 kJ/mol. The particle size did not show significant effect on the rate of gasification. Hydrogen and carbon monoxide appeared to retard the onset of the gasification process. (author)

Preto, Fernando; Zhang, Xiaojie (Frank); Wang, Jinsheng [CANMET Energy Technology Centre, Natural Resources (Canada)

2008-07-15T23:59:59.000Z

316

Incorporation of catalytic dehydrogenation into Fischer-Tropsch synthesis to lower carbon dioxide emissions  

DOE Patents [OSTI]

A method for producing liquid fuels includes the steps of gasifying a starting material selected from a group consisting of coal, biomass, carbon nanotubes and mixtures thereof to produce a syngas, subjecting that syngas to Fischer-Tropsch synthesis (FTS) to produce a hyrdrocarbon product stream, separating that hydrocarbon product stream into C1-C4 hydrocarbons and C5+ hydrocarbons to be used as liquid fuels and subjecting the C1-C4 hydrocarbons to catalytic dehydrogenation (CDH) to produce hydrogen and carbon nanotubes. The hydrogen produced by CDH is recycled to be mixed with the syngas incident to the FTS reactor in order to raise the hydrogen to carbon monoxide ratio of the syngas to values of 2 or higher, which is required to produce liquid hydrocarbon fuels. This is accomplished with little or no production of carbon dioxide, a greenhouse gas. The carbon is captured in the form of a potentially valuable by-product, multi-walled carbon nanotubes (MWNT), while huge emissions of carbon dioxide are avoided and very large quantities of water employed for the water-gas shift in traditional FTS systems are saved.

Huffman, Gerald P

2012-09-18T23:59:59.000Z

317

Carbon Fiber Consortium | Partnerships | ORNL  

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

Carbon Fiber Consortium SHARE Carbon Fiber Consortium Oak Ridge Carbon Fiber Composites Consortium The Oak Ridge Carbon Fiber Composites Consortium was established in 2011 to...

318

Effect of low po? on growth of bacteria and on loss of soluble carbon from maize roots under hydroponic conditions  

E-Print Network [OSTI]

to air (20. 9 kPa 02) and to either 0 or 2 kPa 02 as separate treatments for 48 h. Root systems and nutrient solution samples were collected at 12 hour intervals (commencing with the onset of the oxygen treatment) for enumeration of the bacterial... vs. 20. 9 kPa 02). . . . . . . . . . . . 19 Effect of p02 on hexose carbon (HC) in roots and solution (2 kpa vs- 20 F 9 kpa 02) ~ 36 Effect of p02 on bacteria associated with roots and in solution (2 kPa vs. 20. 9 kPa 02) . 46 Effect of p02...

Coker, Dennis Lee

2012-06-07T23:59:59.000Z

319

Carbon Ionic Conductors for use in Novel Carbon-Ion Fuel Cells  

SciTech Connect (OSTI)

Carbon-consuming fuel cells have many potential advantages, including increased efficiency and reduced pollution in power generation from coal. A large amount of work has already been done on coal fuel cells that utilize yttria-stabilized zirconium carbide as an oxygen-ion superionic membrane material. But high-temperature fuel cells utilizing yttria-stabilized zirconium require partial combustion of coal to carbon monoxide before final oxidation to carbon dioxide occurs via utilization of the oxygen- ion zirconia membrane. A carbon-ion superionic membrane material would enable an entirely new class of carbon fuel cell to be developed, one that would use coal directly as the fuel source, without any intervening combustion process. However, a superionic membrane material for carbon ions has not yet been found. Because no partial combustion of coal would be required, a carbon-ion superionic conductor would allow the direct conversion of coal to electricity and pure CO{sub 2} without the formation of gaseous pollutants. The objective of this research was to investigate ionic lanthanide carbides, which have an unusually high carbon-bond ionicity as potential superionic carbide-ion conductors. A first step in this process is the stabilization of these carbides in the cubic structure, and this stabilization has been achieved via the preparation of pseudobinary lanthanide carbides. The diffusion rates of carbon have been measured in these carbides as stabilized to preserve the high temperature cubic structure down to room temperature. To prepare these new compounds and measure these diffusion rates, a novel, oxide-based preparation method and a new C{sup 13}/C{sup 12} diffusion technique have been developed. The carbon diffusion rates in La{sup 0.5}Er{sup 0.5}C{sub 2}, Ce{sup 0.5}Er{sup 0.5}C{sub 2}, and La{sup 0.5}Y{sup 0.5}C{sub 2}, and Ce{sup 0.5}Tm0.5C{sub 2} modified by the addition of 5 wt %Be{sub 2}C, have been determined at temperatures from 850 C to 1150 C. The resulting diffusion constants as measured were all less than 10{sup -11} cm{sup 2}/sec, and therefore these compounds are not superionic. However, there remain a large number of potentially superionic pseudobinary lanthanide compounds and a number of alternate ionic carbides which might act as dopants to produce vacancies on the carbon-ion sublattice and thereby increase carbon-ion diffusion rates. The discovery of a superionic carbon conductor would usher in a truly revolutionary new coal technology, and could dramatically improve the way in which we generate electricity from coal. The work completed to date is a promising first step towards this end.

Franklin H. Cocks; W. Neal Simmons; Paul A. Klenk

2005-11-01T23:59:59.000Z

320

Carbon Sequestration Project Portfolio  

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

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

Note: This page contains sample records for the topic "hc carbon monoxide" 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

CALIFORNIA CARBON SEQUESTRATION THROUGH  

E-Print Network [OSTI]

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

322

Method of making carbon-carbon composites  

DOE Patents [OSTI]

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

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

1993-01-01T23:59:59.000Z

323

Carbon Code Requirements for voluntary carbon sequestration projects  

E-Print Network [OSTI]

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

324

Toward Zero Carbon Energy Production Toward Zero Carbon Energy Production  

E-Print Network [OSTI]

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

Narasayya, Vivek

325

Low Carbon Fuel Standards  

E-Print Network [OSTI]

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

Sperling, Dan; Yeh, Sonia

2009-01-01T23:59:59.000Z

326

Carbon Capture (Carbon Cycle 2.0)  

ScienceCinema (OSTI)

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

Smit, Berend

2011-06-08T23:59:59.000Z

327

Office of HC Strategy Budget and Performance Metrics (HC-50)...  

Broader source: Energy.gov (indexed) [DOE]

and partner agencies on strategic human capital management, performance metrics, workforce analysis and succession planning. Leadership Tony Nguyen Director of the Office...

328

Acetylenic carbon allotrope  

DOE Patents [OSTI]

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

Lagow, R.J.

1998-02-10T23:59:59.000Z

329

The Woodland Carbon Code  

E-Print Network [OSTI]

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

330

Mesoporous carbon materials  

DOE Patents [OSTI]

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

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

2014-09-09T23:59:59.000Z

331

A first principle study for the adsorption and absorption of carbon atom and the CO dissociation on Ir(100) surface  

SciTech Connect (OSTI)

We employ density functional theory to examine the adsorption and absorption of carbon atom as well as the dissociation of carbon monoxide on Ir(100) surface. We find that carbon atoms bind strongly with Ir(100) surface and prefer the high coordination hollow site for all coverages. In the case of 0.75?ML coverage of carbon, we obtain a bridging metal structure due to the balance between Ir–C and Ir–Ir interactions. In the subsurface region, the carbon atom prefers the octahedral site of Ir(100) surface. We find large diffusion barrier for carbon atom into Ir(100) surface (2.70 eV) due to the strong bonding between carbon atom and Ir(100) surface, whereas we find a very small segregation barrier (0.22 eV) from subsurface to the surface. The minimum energy path and energy barrier for the dissociation of CO on Ir(100) surface are obtained by using climbing image nudge elastic band. The energy barrier of CO dissociation on Ir(100) surface is found to be 3.01 eV, which is appreciably larger than the association energy (1.61 eV) of this molecule.

Erikat, I. A., E-mail: ihsanas@yahoo.com [Department of Physics, Jerash University, Jerash-26150 (Jordan); Hamad, B. A. [Department of Physics, The University of Jordan, Amman-11942 (Jordan)] [Department of Physics, The University of Jordan, Amman-11942 (Jordan)

2013-11-07T23:59:59.000Z

332

Ultrafast Nonlinear Spectroscopy of Semiconducting Carbon Nanotubes  

E-Print Network [OSTI]

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

Graham, Matthew Werden

2010-01-01T23:59:59.000Z

333

Ultrafast Nonlinear Spectroscopy of Semiconducting Carbon Nanotubes  

E-Print Network [OSTI]

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

Graham, Matthew Werden

2010-01-01T23:59:59.000Z

334

R93HC.PDF  

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

Table 3.7a. Space Heating by Census Region and Climate Zone, Table 3.7a. Space Heating by Census Region and Climate Zone, Million U.S. Households, 1993 Space Heating Characteristics RSE Column Factor: Total Census Region Climate Zone RSE Row Factors Northeast Midwest South West Fewer than 2,000 CDD and -- More than 2,000 CDD and Few- er than 4,000 HDD More than 7,000 HDD 5,500 to 7,000 HDD 4,000 to 5,499 HDD Few- er than 4,000 HDD 0.5 0.9 1.1 0.8 0.8 1.6 1.3 1.2 1.2 1.1 Total ................................................. 96.6 19.5 23.3 33.5 20.4 8.7 26.5 22.5 17.8 21.2 7.7 Main Heating Fuel and Equipment Natural Gas .................................... 50.8 9.4 16.8 12.7 11.9 4.3 17.5 10.1 10.2 8.7 7.5 Central Warm-Air Furnace ........... 34.9 4.7 13.4 8.7 8.2 3.2 12.7 6.5 6.3 6.3 9.1 For One Housing Unit ................ 34.1 4.4 13.1 8.6 8.0 3.1 12.4 6.2 6.3 6.2

335

R93HC.PDF  

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

0a. Light Usage by Census Region and Climate Zone, 0a. Light Usage by Census Region and Climate Zone, Million U.S. Households, 1993 Light Usage RSE Column Factor: Total Census Region Climate Zone RSE Row Factors Northeast Midwest South West Fewer than 2,000 CDD and -- More than 2,000 CDD and Few- er than 4,000 HDD More than 7,000 HDD 5,500 to 7,000 HDD 4,000 to 5,499 HDD Few- er than 4,000 HDD 0.4 0.8 0.8 0.6 0.8 2.4 1.4 1.3 1.4 1.1 Total ..................................................... 96.6 19.5 23.3 33.5 20.4 8.7 26.5 22.5 17.8 21.2 6.6 Indoor Electric Lights Total Number Lights 1 to 4 Hours None ............................................... 9.6 2.1 1.5 3.6 2.4 0.7 2.3 1.9 2.2 2.5 10.9 1 ...................................................... 22.1 4.2 5.5 8.0 4.4 2.2 6.2 4.7 4.2 4.9 7.8 2 ......................................................

336

R93HC.PDF  

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

7a. Conservation by Census Region and Climate Zone, 7a. Conservation by Census Region and Climate Zone, Million U.S. Households, 1993 Conservation-Related Items RSE Column Factor: Total Census Region Climate Zone RSE Row Factors Northeast Midwest South West Fewer than 2,000 CDD and -- More than 2,000 CDD and Few- er than 4,000 HDD More than 7,000 HDD 5,500 to 7,000 HDD 4,000 to 5,499 HDD Few- er than 4,000 HDD 0.4 0.8 0.8 0.7 0.8 2.3 1.4 1.3 1.5 1.2 Total ..................................................... 96.6 19.5 23.3 33.5 20.4 8.7 26.5 22.5 17.8 21.2 6.5 Adequacy of Insulation (all households) Well Insulated ..................................... 36.0 7.2 8.8 13.1 6.9 3.5 10.3 8.1 5.9 8.2 6.2 Adequately Insulated .......................... 38.4 8.1 9.5 12.7 8.1 3.5 10.3 9.4 6.8 8.5 5.2 Poorly Insulated .................................. 22.2 4.2 5.0 7.7

337

R93HC.PDF  

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

3a. Usage Indicators by Census Region and Climate Zone, 3a. Usage Indicators by Census Region and Climate Zone, Million U.S. Households, 1993 Usage Indicators RSE Column Factor: Total Census Region Climate Zone RSE Row Factors Northeast Midwest South West Fewer than 2,000 CDD and -- More than 2,000 CDD and Few- er than 4,000 HDD More than 7,000 HDD 5,500 to 7,000 HDD 4,000 to 5,499 HDD Few- er than 4,000 HDD 0.4 0.8 0.8 0.7 0.7 2.5 1.4 1.3 1.5 1.2 Total ..................................................... 96.6 19.5 23.3 33.5 20.4 8.7 26.5 22.5 17.8 21.2 6.4 Weekday Home Activities Home Used for Business Yes ................................................... 6.1 1.0 1.5 2.0 1.6 0.7 1.8 1.1 1.3 1.3 11.4 No ..................................................... 90.5 18.5 21.8 31.5 18.7 8.0 24.7 21.4 16.5 19.9 6.5 Energy-Intensive Activity Yes ...................................................

338

R93HC.PDF  

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

1a. Equipment Purchase by Census Region and Climate Zone, 1a. Equipment Purchase by Census Region and Climate Zone, Million U.S. Households, 1993 Equipment Purchase and Purchase Considerations RSE Column Factor: Total Census Region Climate Zone RSE Row Factors Northeast Midwest South West Fewer than 2,000 CDD and -- More than 2,000 CDD and Few- er than 4,000 HDD More than 7,000 HDD 5,500 to 7,000 HDD 4,000 to 5,499 HDD Few- er than 4,000 HDD 0.5 1.0 0.8 0.7 0.9 2.1 1.1 1.1 1.4 1.1 Total ..................................................... 96.6 19.5 23.3 33.5 20.4 8.7 26.5 22.5 17.8 21.2 7.4 Main Heating System Purchased After January 1, 1990 No ....................................................... 83.6 17.0 20.2 27.9 18.5 7.2 23.3 19.7 15.5 18.0 4.2 Yes ..................................................... 13.0 2.4 3.1 5.6 1.8 1.5 3.2 2.7 2.3 3.2 10.3 Came with Home Purchase

339

R93HC.PDF  

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

... 1.5 0.4 0.4 0.5 0.3 0.1 0.4 0.5 0.3 0.3 18.9 BlackWhite ... 19.0 3.9 5.5 6.5 3.1 1.7 5.9 4.6 2.9 3.9 7.8...

340

R93HC.PDF  

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

7a. Space Heating by Census Region and Climate Zone, 7a. Space Heating by Census Region and Climate Zone, Million U.S. Households, 1993 Space Heating Characteristics RSE Column Factor: Total Census Region Climate Zone RSE Row Factors Northeast Midwest South West Fewer than 2,000 CDD and -- More than 2,000 CDD and Few- er than 4,000 HDD More than 7,000 HDD 5,500 to 7,000 HDD 4,000 to 5,499 HDD Few- er than 4,000 HDD 0.5 0.9 1.1 0.8 0.8 1.6 1.3 1.2 1.2 1.1 Total ................................................. 96.6 19.5 23.3 33.5 20.4 8.7 26.5 22.5 17.8 21.2 7.7 Main Heating Fuel and Equipment Natural Gas .................................... 50.8 9.4 16.8 12.7 11.9 4.3 17.5 10.1 10.2 8.7 7.5 Central Warm-Air Furnace ........... 34.9 4.7 13.4 8.7 8.2 3.2 12.7 6.5 6.3 6.3 9.1 For One Housing Unit ................ 34.1 4.4 13.1 8.6 8.0 3.1 12.4 6.2 6.3 6.2 9.4

Note: This page contains sample records for the topic "hc carbon monoxide" 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

Purification and Processing of Graphitic Carbons  

E-Print Network [OSTI]

N-Dimethylformamide EA Electric Arc-Discharge HC Hydrocarbonmethods include electric arc-discharge (EA), 18, 19 laserSWNTs prepared by electric arc-discharge were obtained from

Worsley, Kimberly Anne

2010-01-01T23:59:59.000Z

342

JOURNAL OF GEOPHYSICAL RESEARCH, VOL. 106, NO. D22, PAGES28,481-28,495, NOVEMBER 27, 2001 Source analysis of carbon monoxide  

E-Print Network [OSTI]

and agricultural waste burning in India are major CO sources for the Indian Ocean north of the ITCZ, with minor the globe where biofuel use and biomass burning contribute so much to the CO mixing ratios. In general, most is the dominant CO source at middle and high northern latitudes, whereas biofuel use and biomass burning are major

Laat, Jos de

343

Potentiometric CO titrations of carbon monoxide dehydrogenase and CO-inhibition of the NI-removing reaction with 1,10--phenanthroline  

E-Print Network [OSTI]

the slope and intercept of that plot. Kco was found to be 840 atm ' 30 2400 1900 1 400 ss 0 900 400 ? 100 O. OEO 5. 0E-3 1. 0E-2 1. 5E-2 2. 0E-2 Pco 0. 1 O V -0. 1 ai Z -0. 3 C l -0. 5 tn 4. Z -0. 7 t: ~ I no CO 2. 0 X 10-& otm 4 5.... 1 X 10-3otm 9. 9 X10- otm -0. 9 0 5000 1 0000 1 5000 20000 25000 30000 Time (min) Figure 7. Inhibition of the Reaction of I, IO-Phenanthroline and CODH by CO. See Erperimenral Procedures for details. Upper Panel: Plot of NiFeC signai intensity...

Russell, William Kent

1996-01-01T23:59:59.000Z

344

Method of making a catalytic metal oxide selective for the conversion of a gas and a coating system for the selective oxidation of hydrocarbons and carbon monoxide  

SciTech Connect (OSTI)

A method is described of making a catalytic metal oxide selective to catalyzing the conversion of given gas species, comprising: intimately supporting a solid film of catalytic metal oxide on an electrically conducting material, said film having an exposed outer surface spaced no greater than 1,000 angstroms from said conducting material and said conducting material being matched to the composition of said oxide to change the electron state of the exposed outer surface to promote a reaction between given gas species and said oxide, said metal oxide being selected from the group consisting of TiO[sub 2], SnO[sub 2], FeO, SrTiO[sub 3], and CoO, and said conducting material being selected from the group consisting of Au, Pt, TiN, Pd, Rh, Ni, and Co.

Logothetis, E.M.; Soltis, R.E.

1993-07-20T23:59:59.000Z

345

Surface structure of coadsorbed benzene and carbon monoxide on the rhodium(111) single crystal analyzed with low-energy electron diffraction intensities  

SciTech Connect (OSTI)

The first structural analysis of a molecular coadsorbate system is presented. Mutual reordering and site shifting are found to occur for benzene and CO coadsorbed in a (/sub 13//sup 31/) lattice on Rh(111). This low-energy electron diffraction (LEED) intensity analysis yields the first confirmed hollow-site adsorption of CO on a single-crystal metal surface, with a C-O bond length expanded by 0.06 +/- 0.05 A from the gas phase. The flat-lying benzene is found centered over hcp-type hollow sites with a strong Kekule-type distortion: C-C bond lengths alternate between 1.33 +/- 0.15 A (hydrogen positions were not determined). This suggests the possibility of a 1,3,5-cyclohexatriene species being formed. The Rh-C bond length is 2.35 +/- 0.05 A for benzene and 2.16 +/- 0.04 A for CO.

Van Hove, M.A.; Lin, R.F.; Somorjai, G.A.

1986-05-14T23:59:59.000Z

346

Reductive coupling of carbon monoxide to C{sub 2} products. Progress report for the period, May 1, 1990--November 15, 1993  

SciTech Connect (OSTI)

This progress report covers the two broad areas of research addressed during the period since May 1, 1990. As proposed in 1989, studies of carbyne transformations have been pursued with a variety of carbyne substituents. Perhaps the most noteworthy carbyne results are also the simplest: preparation and properties of the parent M{triple_bond}CH unit. The other topic addressed with DOE support has metal nitrene chemistry as the cornerstone. Publications with iron, tungsten and copper complexes reflect our efforts to access intermediate oxidation state metal nitrene monomers. This new thrust was a central theme of the proposal submitted in 1989, and progress to date is sufficiently encouraging that detailed plans for expanding our nitrene project are an integral part of the accompanying proposal. References in this progress report are kept to a minimum; extensive references in the papers cited here place the work in perspective relative to the literature landscape.

Templeton, J.L.

1993-10-01T23:59:59.000Z

347

THE IMPACT OF REDUCED VENTILATION ON INDOOR AIR QUALITY IN RESIDENTIAL BUILDINGS  

E-Print Network [OSTI]

carbon monoxide and nitrogen dioxide fron gas appliances;quality, infiltration, nitrogen dioxide, radon, ventilation.carbon monoxide (CO), nitrogen dioxide (N02)• formaldehyde (

Berk, James V.

2013-01-01T23:59:59.000Z

348

BUILDING VENTILATION AND INDOOR AIR QUALITY PROGRAM. CHAPTER FROM ENERGY AND ENVIRONMENT DIVISION ANNUAL REPORT 1978  

E-Print Network [OSTI]

Critical Analysis of Nitrogen Dioxide Air Quality Standards.22 Gaseous Emissions: Nitrogen Dioxide, Carbon Monoxide,3- 4 GASEOUS EMISSIONS: NITROGEN DIOXIDE, CARBON MONOXIDE,

Cairns, Elton J.

2011-01-01T23:59:59.000Z

349

Carbon International | Open Energy Information  

Open Energy Info (EERE)

Kingdom Zip: NW1 8LH Sector: Carbon Product: London-based energy and communications agency specialising in low carbon energy and climate change. References: Carbon...

350

Carbon Nanostructure-Based Sensors  

E-Print Network [OSTI]

Control of Single-Walled Carbon Nanotube Functionalization.M. S. Characterizing carbon nanotube samples with resonancewith a Single-Walled Carbon Nanotube Capacitor. Science

Sarkar, Tapan

2012-01-01T23:59:59.000Z

351

Method of making carbon-carbon composites  

DOE Patents [OSTI]

A process for making a carbon-carbon composite having a combination of high crystallinity, high strength, high modulus and high thermal and electrical conductivity. High-modulus/high-strength mesophase derived carbon fibers are woven into a suitable cloth. Layers of this easily graphitizable woven cloth are covered with petroleum or coal tar pitch and pressed at a temperature a few degrees above the softening point of the pitch to form a green laminated composite. The green composite is restrained in a suitable fixture and heated slowly to carbonize the pitch binder. The carbonized composite is then impregnated several times with pitch by covering the composite with hot pitch under pressure. The composites are given a heat treatment between each impregnation step to crack up the infiltrated carbon and allow additional pitch to enter the microstructure during the next impregnation cycle. The impregnated composites are then given a final heat treatment in the range 2500.degree. to 3000.degree. C. to fully graphitize the fibers and the matrix carbon. The composites are then infiltrated with pyrolytic carbon by chemical vapor deposition in the range 1000.degree. to 1300.degree. C. at a reduced pressure for approximately one hundred and fifty (150) hours.

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

1991-01-01T23:59:59.000Z

352

Carbon nanotube nanoelectrode arrays  

DOE Patents [OSTI]

The present invention relates to microelectode arrays (MEAs), and more particularly to carbon nanotube nanoelectrode arrays (CNT-NEAs) for chemical and biological sensing, and methods of use. A nanoelectrode array includes a carbon nanotube material comprising an array of substantially linear carbon nanotubes each having a proximal end and a distal end, the proximal end of the carbon nanotubes are attached to a catalyst substrate material so as to form the array with a pre-determined site density, wherein the carbon nanotubes are aligned with respect to one another within the array; an electrically insulating layer on the surface of the carbon nanotube material, whereby the distal end of the carbon nanotubes extend beyond the electrically insulating layer; a second adhesive electrically insulating layer on the surface of the electrically insulating layer, whereby the distal end of the carbon nanotubes extend beyond the second adhesive electrically insulating layer; and a metal wire attached to the catalyst substrate material.

Ren, Zhifeng (Newton, MA); Lin, Yuehe (Richland, WA); Yantasee, Wassana (Richland, WA); Liu, Guodong (Fargo, ND); Lu, Fang (Burlingame, CA); Tu, Yi (Camarillo, CA)

2008-11-18T23:59:59.000Z

353

Quantifying Carbon Cycle Feedbacks  

Science Journals Connector (OSTI)

Perturbations to the carbon cycle could constitute large feedbacks on future changes in atmospheric CO2 concentration and climate. This paper demonstrates how carbon cycle feedback can be expressed in formally similar ways to climate feedback, ...

J. M. Gregory; C. D. Jones; P. Cadule; P. Friedlingstein

2009-10-01T23:59:59.000Z

354

Terrestrial Carbon Management  

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

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

355

Supernova: Carbon detonation redux  

Science Journals Connector (OSTI)

... A DECADE ago carbon detonation was all the rage among supernova theorists. The idea was that the characteristic burst ... wind.

J. Craig Wheeler

1983-03-17T23:59:59.000Z

356

Carbon Capital | Open Energy Information  

Open Energy Info (EERE)

Sector: Carbon Product: Manages a carbon fund specialised in forestry projects References: Carbon Capital1 This article is a stub. You can help OpenEI by expanding it. Carbon...

357

Kinetics Of Carbon Gasification  

Science Journals Connector (OSTI)

Kinetics Of Carbon Gasification ... The steam–carbon reaction, which is the essential reaction of the gasification processes of carbon-based feed stocks (e.g., coal and biomass), produces synthesis gas (H2 + CO), a synthetically flexible, environmentally benign energy source. ... Coal Gasification in CO2 and Steam:? Development of a Steam Injection Facility for High-Pressure Wire-Mesh Reactors ...

C. W. Zielke; Everett. Gorin

1957-03-01T23:59:59.000Z

358

How Carbon Capture Works  

Broader source: Energy.gov [DOE]

Carbon capture, utilization and storage is a process that captures carbon dioxide emissions from sources like coal-fired power plants and either reuses or stores it so it will not enter the atmosphere. We'll break down the process step by step so you can learn how this technology can help us lower our carbon pollution.

359

Intro to Carbon Sequestration  

ScienceCinema (OSTI)

NETL's Carbon Sequestration Program is helping to develop technologies to capture, purify, and store carbon dioxide (CO2) in order to reduce greenhouse gas emissions without adversely influencing energy use or hindering economic growth. Carbon sequestration technologies capture and store CO2 that would otherwise reside in the atmosphere for long periods of time.

None

2010-01-08T23:59:59.000Z

360

Carbon Connections | Open Energy Information  

Open Energy Info (EERE)

Product: Carbon Connections links partner universities with industry encouraging knowledge exchange and developing innovative ideas. References: Carbon Connections1 This...

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


361

Carbon in detonations  

SciTech Connect (OSTI)

We review three principal results from a five year study of carbon and its properties in detonations and discuss the implications of these results to the behavior of explosives. We first present a new determination of the carbon melt line from release wave velocity measurements in the shocked state. We then outline a colloidal theory of carbon clustering which from diffusion limited coagulation predicts a slow energy release rate for the carbon chemistry. Finally, we show the results from the examination of recovered soot. Here we see support for the colloid theory and find the diamond phase of carbon. The main theme of this paper is that the carbon in detonation products is in the form of a colloidal suspension of carbon clusters which grow through diffusion limited collisions. Even the final state is not bulk graphite or diamond, but is a collection of small, less than 100 /angstrom/A, diamond and graphitic clusters. 23 refs., 4 figs.

Johnson, J.D.

1989-01-01T23:59:59.000Z

362

Molecular Basis of Microbial One-Carbon Metabolism 2008 Gordon Research Conference (July 20-25, 2008)  

SciTech Connect (OSTI)

One-carbon (C-1) compounds play a central role in microbial metabolism. C-1 compounds include methane, carbon monoxide, CO2, and methanol as well as coenzyme-bound one-carbon compounds (methyl-B12, CH3-H4folate, etc). Such compounds are of broad global importance because several C-1 compounds (e.g., CH4) are important energy sources, some (e.g., CO2 and CH4) are potent greenhouse gases, and others (e.g., CH2Cl2) are xenobiotics. They are central in pathways of energy metabolism and carbon fixation by microbes and many are of industrial interest. Research on the pathways of one-carbon metabolism has added greatly to our understanding of evolution, structural biology, enzyme mechanisms, gene regulation, ecology, and applied biology. The 2008 meeting will include recent important findings in the following areas: (a) genomics, metagenomics, and proteomic studies that have expanded our understanding of autotrophy and C-1 metabolism and the evolution of these pathways; (b) redox regulation of carbon cycles and the interrelationship between the carbon cycle and other biogeochemical cycles (sulfur, nitrogen, oxygen); (c) novel pathways for carbon assimilation; (d) biotechnology related to C-1 metabolism; (e) novel enzyme mechanisms including channeling of C-1 intermediates during metabolism; and (f) the relationship between metal homeostasis and the global carbon cycle. The conference has a diverse and gender-balanced slate of speakers and session leaders. The wide variety of disciplines brought to the study of C-1 metabolism make the field an excellent one in which to train young researchers.

Stephen W. Ragsdale

2009-08-12T23:59:59.000Z

363

Potential of Silicon Carbide-Derived Carbon for Carbon Capture  

Science Journals Connector (OSTI)

Potential of Silicon Carbide-Derived Carbon for Carbon Capture ... In contrast to conventional carbons made from natural precursors, carbide derived carbons (CDCs),(8, 10-13) being synthesized from an inorganic source, have no polar functional groups and are composed of purely covalently bonded carbon. ...

S. K. Bhatia; T. X. Nguyen

2011-08-08T23:59:59.000Z

364

Carbon Sequestration via Mineral Carbonation: Overview and Assessment  

E-Print Network [OSTI]

1 Carbon Sequestration via Mineral Carbonation: Overview and Assessment 14 March 2002 Howard Herzog overview and assessment of carbon sequestration by mineral carbonation (referred to as "mineral sequestration R&D. The first is that carbonates have a lower energy state than CO2. Therefore, at least

365

Carbon RRLs Carbon RRLs towards Ultra-compact HII Regions  

E-Print Network [OSTI]

Carbon RRLs Carbon RRLs towards Ultra-compact HII Regions Dana S. Balser D. Anish Roshi (Raman (Agnes Scott College) #12;Carbon RRLs Carbon Radio Recombination Lines (RRLs) NGC 2024 (Orion B) IC 1795 (W3) Palmer et al. (1967) #12;Carbon RRLs Photodissociation Regions (PDRs) Hollenbach & Tielens (1997

Balser, Dana S.

366

Would Border Carbon Adjustments prevent carbon leakage and heavy industry  

E-Print Network [OSTI]

No 52-2013 Would Border Carbon Adjustments prevent carbon leakage and heavy industry halshs-00870689,version1-7Oct2013 #12;Would Border Carbon Adjustments prevent carbon leakage and heavy The efficiency of unilateral climate policies may be hampered by carbon leakage and competitiveness losses

Paris-Sud XI, Université de

367

Cumulative Carbon and Just Allocation of the Global Carbon Commons  

E-Print Network [OSTI]

Cumulative Carbon and Just Allocation of the Global Carbon Commons R.T. Pierrehumbert1 on climate can be characterized by a single statistic, called Cumulative Carbon. This is the aggregate amount of carbon emitted in the form of carbon dioxide by activities such as fossil fuel burning and deforestation

Pierrehumbert, Raymond

368

Carbon Emissions: Food Industry  

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

Food Industry Food Industry Carbon Emissions in the Food Industry The Industry at a Glance, 1994 (SIC Code: 20) Total Energy-Related Emissions: 24.4 million metric tons of carbon (MMTC) -- Pct. of All Manufacturers: 6.6% Total First Use of Energy: 1,193 trillion Btu -- Pct. of All Manufacturers: 5.5% Carbon Intensity: 20.44 MMTC per quadrillion Btu Energy Information Administration, "1994 Manufacturing Energy Consumption Survey" and Emissions of Greenhouse Gases in the United States 1998 Energy-Related Carbon Emissions, 1994 Source of Carbon Carbon Emissions (million metric tons) All Energy Sources 24.4 Net Electricity 9.8 Natural Gas 9.1 Coal 4.2 All Other Sources 1.3 Energy Information Administration, "1994 Manufacturing Energy Consumption Survey" and Emissions of Greenhouse Gases in the United States 1998

369

Carbon Emissions: Chemicals Industry  

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

Chemicals Industry Chemicals Industry Carbon Emissions in the Chemicals Industry The Industry at a Glance, 1994 (SIC Code: 28) Total Energy-Related Emissions: 78.3 million metric tons of carbon (MMTC) -- Pct. of All Manufacturers: 21.1% -- Nonfuel Emissions: 12.0 MMTC Total First Use of Energy: 5,328 trillion Btu -- Pct. of All Manufacturers: 24.6% Energy Sources Used As Feedstocks: 2,297 trillion Btu -- LPG: 1,365 trillion Btu -- Natural Gas: 674 trillion Btu Carbon Intensity: 14.70 MMTC per quadrillion Btu Energy Information Administration, "1994 Manufacturing Energy Consumption Survey" and Emissions of Greenhouse Gases in the United States 1998 Energy-Related Carbon Emissions, 1994 Source of Carbon Carbon Emissions (million metric tons) All Energy Sources 78.3 Natural Gas 32.1

370

The Carbon Cycle  

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

The Carbon Cycle The Carbon Cycle The global carbon cycle involves the carbon in and exchanging between the earth's atmosphere, fossil fuels, the oceans, and the vegetation and soils of the earth's terrestrial ecosystems. image Each year, the world's terrestrial ecosystems withdraw carbon from the atmosphere through photosynthesis and add it again through respiration and decay. A more detailed look at the global carbon cycle for the 1990s is shown below. The main annual fluxes in GtC yr-1 are: pre-industrial "natural" fluxes in black and "anthropogenic" fluxes in red (modified from Sarmiento and Gruber, 2006, with changes in pool sizes from Sabine et al., 2004a). The net terrestrial loss of -39 GtC is inferred from cumulative fossil fuel emissions minus atmospheric increase minus ocean storage. The loss of

371

Carbon Emissions: Paper Industry  

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

Paper Industry Paper Industry Carbon Emissions in the Paper Industry The Industry at a Glance, 1994 (SIC Code: 26) Total Energy-Related Emissions: 31.6 million metric tons of carbon (MMTC) -- Pct. of All Manufacturers: 8.5% Total First Use of Energy: 2,665 trillion Btu -- Pct. of All Manufacturers: 12.3% -- Pct. Renewable Energy: 47.7% Carbon Intensity: 11.88 MMTC per quadrillion Btu Renewable Energy Sources (no net emissions): -- Pulping liquor: 882 trillion Btu -- Wood chips and bark: 389 trillion Btu Energy Information Administration, "1994 Manufacturing Energy Consumption Survey" and Emissions of Greenhouse Gases in the United States 1998 Energy-Related Carbon Emissions, 1994 Source of Carbon Carbon Emissions (million metric tons) All Energy Sources 31.6 Net Electricity 11.0

372

NETL: Carbon Storage  

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

Storage Storage Technologies Carbon Storage (formerly referred to as the "Carbon Sequestration Program") Program Overview For quick navigation of NETL's Carbon Storage Program website, please click on the image. NETL's Carbon Storage Program Fossil fuels are considered the most dependable, cost-effective energy source in the world. The availability of these fuels to provide clean, affordable energy is essential for domestic and global prosperity and security well into the 21st century. However, a balance is needed between energy security and concerns over the impacts of concentrations of greenhouse gases (GHGs) in the atmosphere - particularly carbon dioxide (CO2). NETL's Carbon Storage Program is developing a technology portfolio of safe, cost-effective, commercial-scale CO2 capture, storage, and mitigation

373

Striving To Capture Carbon  

Science Journals Connector (OSTI)

Striving To Capture Carbon ... Energy ministers from around the world met in Washington, D.C., for three days earlier this month to wrestle with how to reenergize efforts to cut carbon emissions from coal-fired power plants. ... Their solution, not surprisingly, is a rapid acceleration of R&D for technologies that capture and sequester underground carbon dioxide emitted by power plants, refineries, and industrial manufacturers that burn fossil fuels. ...

JEFF JOHNSON

2013-11-25T23:59:59.000Z

374

Paraconductivity in carbon nanotubes  

Science Journals Connector (OSTI)

We report the calculation of paraconductivity in carbon nanotubes above the superconducting transition temperature. The complex behavior of paraconductivity depending upon the tube radius, temperature, and magnetic field strength is analyzed. The results are qualitatively compared with recent experimental observations in carbon nanotubes of an inherent transition to the superconducting state and pronounced thermodynamic fluctuations above Tc. The application of our results to single-wall and multiwall carbon nanotubes as well as ropes of nanotubes is discussed.

D. V. Livanov and A. A. Varlamov

2002-09-27T23:59:59.000Z

375

Kinetic models for uncatalyzed and potassium-catalyzed gasification of char by carbon dioxide  

SciTech Connect (OSTI)

A differential packed-bed reactor has been employed to study the gasification of uncatalyzed and 7.5 wt% K/sub 2/CO/sub 3/-catalyzed Saran char in carbon dioxide/carbon monoxide mixtures at a total pressure near 1 atm (101.3 kPa). The gasification temperature was varied between 1131 and 1229 K for the uncatalyzed case, and between 922 and 1046 K for the catalyzed case. Gasification rate data were tested with a model which involves two-site adsorption and subsequent dissociation of CO/sub 2/ on the char surface. The results indicate that this model adequately explains both the uncatalyzed and catalyzed gasification data. However, higher concentrations of carbon-oxygen complex, (C(O)), exist on the surface during catalyzed gasification. The increase in (C(O)) weakens carbon-carbon bonds and thus lowers the activation energy for desorption of the C(O) complex. Adsorption of CO and CO/sub 2/ on both catalyzed and uncatalyzed chars was also followed with a volumetric adsorption apparatus at pressures between 1 and 100 kPa and temperatures from 273 to 725 K. The catalyzed char adsorbed an order of magnitude more CO/sub 2/ at 559 K than the uncatalyzed char. Subsequent dissociation of CO/sub 2/ on the carbon surface does not appear to be catalyzed by potassium. Thus, the catalysts' role is to augment the efficiency and/or number of sites for CO/sub 2/ adsorption, thereby creating more oxygen on the surface. The higher rate during catalyzed gasification can be attributed to a combination of increased (C(O)) and a smaller activation energy for desorption of C(O).

Koenig, P.C.

1985-01-01T23:59:59.000Z

376

Carbon Sequestration - Public Meeting  

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

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

377

NETL: Carbon Storage - Infrastructure  

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

Infrastructure Infrastructure Carbon Storage Infrastructure The Infrastructure Element of DOE's Carbon Storage Program is focused on research and development (R&D) initiatives to advance geologic CO2 storage toward commercialization. DOE determined early in the program's development that addressing CO2 mitigation on a regional level is the most effective way to address differences in geology, climate, population density, infrastructure, and socioeconomic development. This element includes the following efforts designed to support the development of regional infrastructure for carbon capture and storage (CCS). Click on Image to Navigate Infrastructure Content on this page requires a newer version of Adobe Flash Player. Get Adobe Flash player Regional Carbon Sequestration Partnerships (RCSP) - This

378

Carbon Sequestration 101  

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

R&D Overview R&D Overview Office of Fossil Energy Justin "Judd" R. Swift Asst. Secretary for International Affairs Office of Fossil Energy U.S. Department of Energy 2 nd U.S/China CO 2 Emission Control Science & Technology Symposium May 28-29, 2008 Hangzhou, China Office of Fossil Energy Technological Carbon Management Options Improve Efficiency Sequester Carbon ï‚· Renewables ï‚· Nuclear ï‚· Fuel Switching ï‚· Demand Side ï‚· Supply Side ï‚· Capture & Store ï‚· Enhance Natural Sinks Reduce Carbon Intensity All options needed to: ï‚· Affordably meet energy demand ï‚· Address environmental objectives Office of Fossil Energy DOE's Sequestration Program Structure Infrastructure Regional Carbon Sequestration

379

Activated Carbon Injection  

ScienceCinema (OSTI)

History of the Clean Air Act and how the injection of carbon into a coal power plant's flu smoke can reduce the amount of mercury in the smoke.

None

2014-07-22T23:59:59.000Z

380

Carbon Capture and Storage  

Science Journals Connector (OSTI)

Shift to alternative energy sources, which have been introduced in Chap.  8 .... They are effective in air pollution control as well as carbon

Zhongchao Tan

2014-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "hc carbon monoxide" 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

Composites of Carbon Nanotubes.  

E-Print Network [OSTI]

??The purpose of this research was to study various methods of incorporation of single-walled carbon nanotubes (SWNT) with polymers for producing electrically conductive polystyrene composites.… (more)

Tchoul, Maxim N.

2008-01-01T23:59:59.000Z

382

Reinforced Carbon Nanotubes.  

DOE Patents [OSTI]

The present invention relates generally to reinforced carbon nanotubes, and more particularly to reinforced carbon nanotubes having a plurality of microparticulate carbide or oxide materials formed substantially on the surface of such reinforced carbon nanotubes composite materials. In particular, the present invention provides reinforced carbon nanotubes (CNTs) having a plurality of boron carbide nanolumps formed substantially on a surface of the reinforced CNTs that provide a reinforcing effect on CNTs, enabling their use as effective reinforcing fillers for matrix materials to give high-strength composites. The present invention also provides methods for producing such carbide reinforced CNTs.

Ren, Zhifen (Newton, MA); Wen, Jian Guo (Newton, MA); Lao, Jing Y. (Chestnut Hill, MA); Li, Wenzhi (Brookline, MA)

2005-06-28T23:59:59.000Z

383

Carbon Fiber SMC  

Broader source: Energy.gov (indexed) [DOE]

110,000 ACC capital) in 2008 * 54,000 for 2009 Partners * Continental Structural Plastic (CSP), a Tier One supplier * Discounted compounding and molding * Zoltek, a carbon...

384

Carbon Fiber Technology Facility  

Broader source: Energy.gov (indexed) [DOE]

- 4M AMO - 1.5M VTP - Remainder covered by carry- over and ARRA project contingency * Cost of carbon fiber * Technology scaling * Market development * Workforce development * Oak...

385

Activated Carbon Injection  

SciTech Connect (OSTI)

History of the Clean Air Act and how the injection of carbon into a coal power plant's flu smoke can reduce the amount of mercury in the smoke.

None

2014-07-16T23:59:59.000Z

386

NETL: Carbon Storage - Reference Shelf  

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

Carbon Storage > Reference Shelf Carbon Storage > Reference Shelf Carbon Storage Reference Shelf Below are links to Carbon Storage Program documents and reference materials. Each of the 10 categories has a variety of documents posted for easy access to current information - just click on the category link to view all related materials. RSS Icon Subscribe to the Carbon Storage RSS Feed. Carbon Storage Collage 2012 Carbon Utilization and Storage Atlas IV Carbon Sequestration Project Portfolio DOE/NETL Carbon Dioxide Capture and Storage RD&D Roadmap Public Outreach and Education for Carbon Storage Projects Carbon Storage Technology Program Plan Carbon Storage Newsletter Archive Impact of the Marcellus Shale Gas Play on Current and Future CCS Activities Site Screening, Selection, and Initial Characterization for Storage of CO2 in Deep Geologic Formations Carbon Storage Systems and Well Management Activities Monitoring, Verification, and Accounting of CO2 Stored in Deep Geologic Formations

387

SGL Carbon AG | Open Energy Information  

Open Energy Info (EERE)

Carbon AG Jump to: navigation, search Name: SGL Carbon AG Place: Wiesbaden, Hessen, Germany Zip: 65203 Sector: Carbon Product: A Germany-based manufacturer of carbon-based...

388

Eon Masdar Integrated Carbon | Open Energy Information  

Open Energy Info (EERE)

Carbon Jump to: navigation, search Name: Eon Masdar Integrated Carbon Place: Germany Sector: Carbon Product: Germany-based carbon emission projects developer. References:...

389

EMBODIED CARBON TARIFFS Christoph Bhringer  

E-Print Network [OSTI]

EMBODIED CARBON TARIFFS Christoph Böhringer Jared C. Carbone Thomas F. Rutherford Revised: August 2013 Abstract Embodied carbon tariffs tax the direct and indirect carbon emissions embodied in trade -- an idea popularized by countries seeking to extend the reach of domestic carbon regu- lations. We

390

Carbon-Optimal and Carbon-Neutral Supply Chains  

E-Print Network [OSTI]

Y. Li, M. Daskin. 2009. Carbon Footprint and the ManagementJ. van Houtum. 2011. E?ect of carbon emission regulations onStreamlined Enterprise Carbon Footprinting. Environmental

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

2011-01-01T23:59:59.000Z

391

Global Carbon Cycle, Carbon Dioxide Emissions and Mitigation  

Science Journals Connector (OSTI)

The carbon cycle is one of the biogeochemical cycles and describes the movement of carbon, in its many forms, within the biosphere, atmosphere, oceans and geosphere. The global carbon cycle involves the earth’...

2008-01-01T23:59:59.000Z

392

Adsorption and methanation of carbon dioxide on a nickel/silica catalyst  

SciTech Connect (OSTI)

The adsorption and methanation of carbon dioxide on a nickel/silica catalyst were studied using temperature-programmed desorption and temperature-programmed reaction. Carbon dioxide adsorption on nickel was found to be activated; almost no adsorption occurred at room temperature, but large coverages were obtained between 383 and 473 K. The data indicate CO/sub 2/ dissociates upon adsorption at elevated temperatures to yield carbon monoxide and oxygen atoms. These oxygen atoms react with hydrogen at room temperature, so the methane and water observed during programmed heating in flowing hydrogen are identical for adsorbed CO and adsorbed CO/sub 2/. Single CH/sub 4/ and H/sub 2/O peaks, each with a peak temperature at 473 K, were observed. This peak temperature did not change with initial coverage, indicating methanation is first order in CO surface coverage. The activated adsorption of CO/sub 2/ allowed these coverage variation experiments to be carried out. Thus, following adsorption, CO and CO/sub 2/ methanation proceed by the same mechanism. However, the activated adsorption of CO/sub 2/ may create a higher H/sub 2/:CO surface ratio during steady-state hydrogenation, causing CO/sub 2/ hydrogenation to favor methane over higher hydrocarbons. 5 figures.

Falconer, J.L.; Zagli, A.E.

1980-04-01T23:59:59.000Z

393

Carbonation Mechanism of Reservoir Rock by Supercritical Carbon...  

Broader source: Energy.gov (indexed) [DOE]

the carbonation reaction mechanisms between supercritical carbon dioxide (scCO2) and reservoir rocks consisting of different mineralogical compositions in aqueous and...

394

Metal-organic frameworks with high capacity and selectivity for harmful gases  

E-Print Network [OSTI]

, chlorine, tetrahydrothiophene, benzene, dichloromethane, ethyl- ene oxide, and carbon monoxide. Kinetic

Yaghi, Omar M.

395

In situ gas-phase catalytic properties of TiC-supported size-selected gold nanoparticles synthesized by diblock copolymer encapsulation  

E-Print Network [OSTI]

nanoparticle; Titanium carbide; Carbon monoxide; Oxygen; Diblock copolymer; Thermal desorption spectroscopy

Kik, Pieter

396

How can I make sure my rented property is safe?  

E-Print Network [OSTI]

, carbon monoxide, lack of space, security or lighting, or excessive noise. poor hygiene, sanitation

Royal Holloway, University of London

397

Nanomechanics of carbon nanotubes  

Science Journals Connector (OSTI)

...nanotechnology II Nanomechanics of carbon nanotubes Andras Kis 1 * Alex Zettl 2 3 * * Authors...important potential applications of carbon nanotubes are related to their mechanical properties...characterization of the mechanical properties of nanotubes includes a rich variety of experiments...

2008-01-01T23:59:59.000Z

398

Fly ash carbon passivation  

DOE Patents [OSTI]

A thermal method to passivate the carbon and/or other components in fly ash significantly decreases adsorption. The passivated carbon remains in the fly ash. Heating the fly ash to about 500 and 800 degrees C. under inert gas conditions sharply decreases the amount of surfactant adsorbed by the fly ash recovered after thermal treatment despite the fact that the carbon content remains in the fly ash. Using oxygen and inert gas mixtures, the present invention shows that a thermal treatment to about 500 degrees C. also sharply decreases the surfactant adsorption of the recovered fly ash even though most of the carbon remains intact. Also, thermal treatment to about 800 degrees C. under these same oxidative conditions shows a sharp decrease in surfactant adsorption of the recovered fly ash due to the fact that the carbon has been removed. This experiment simulates the various "carbon burnout" methods and is not a claim in this method. The present invention provides a thermal method of deactivating high carbon fly ash toward adsorption of AEAs while retaining the fly ash carbon. The fly ash can be used, for example, as a partial Portland cement replacement in air-entrained concrete, in conductive and other concretes, and for other applications.

La Count, Robert B; Baltrus, John P; Kern, Douglas G

2013-05-14T23:59:59.000Z

399

Electronic Properties of Carbon Nanotubes  

E-Print Network [OSTI]

P. Avouris, in Carbon Nanotubes M. S. Dresselhaus, P.Physics of Carbon Nanotubes S. V. Rotkin, S. Subramoney,Properties of Carbon Nanotubes Philip G. Collins 1 and

Collins, Philip G

2008-01-01T23:59:59.000Z

400

Carbon Sequestration: A Comparative Analysis  

Science Journals Connector (OSTI)

Carbon sequestration refers to the provision and safe storage of carbon dioxide that otherwise would be emitted to ... isolation, and final storage of the produced carbon dioxide, utilizing biological, chemical, ...

Christopher J. Koroneos; Dimitrios C. Rovas

2010-01-01T23:59:59.000Z

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


401

Electronic Properties of Carbon Nanotubes  

E-Print Network [OSTI]

P. Avouris, in Carbon Nanotubes M. S. Dresselhaus, P.in Applied Physics of Carbon Nanotubes S. V. Rotkin, S.Electronic Properties of Carbon Nanotubes Philip G. Collins

Collins, Philip G

2008-01-01T23:59:59.000Z

402

Carbon-free generation  

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

Carbon-free generation Carbon-free generation Carbon-free central generation of electricity, either through fossil fuel combustion with carbon dioxide capture and storage or development of renewable sources such as solar, wind, and/or nuclear power, is key to our future energy portfolio. Brookhaven also provides tools and techniques for studying geological carbon dioxide sequestration and analyzing safety issues for nuclear systems. Our nation faces grand challenges: finding alternative and cleaner energy sources and improving efficiency to meet our exponentially growing energy needs. Researchers at Brookhaven National Laboratory are poised to meet these challenges with basic and applied research programs aimed at advancing the effective use of renewable energy through improved conversion,

403

2013 Global Carbon Project  

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

2013 Global Carbon Project 2013 Global Carbon Project DOI: 10.3334/CDIAC/GCP_2013_V1.1 image 2013 Budget v1.1 (November 2013) image 2013 Budget v1.3 (December 2013, contains typographical corrections to 2011 Australia emissions from v1.1 and corrections to the 2011 Australia transfer and consumption emissions from v1.2) image image image image Global Carbon Dioxide Emissions to Reach 36 Billion Tonnes in 2013 Global emissions of carbon dioxide from the combustion of fossil fuels will reach 36 billion tonnes for the year 2013. "This is a level unprecedented in human history," says CSIRO's Dr Pep Canadell, Executive-Director of the Global Carbon Project (GCP) and co-author of a new report. Global emissions due to fossil fuel alone are set to grow this year at a slightly lower pace of 2.1% than the average 3.1% since 2000, reaching 36

404

Black Carbon and the Carbon Cycle  

Science Journals Connector (OSTI)

...reduces net CO 2 release by permanent deforestation...constitute a substantial fraction of the “missing carbon...estimate of oxygen release assuming 10% of...constitute a substantial fraction of sedimentary organic...formation by vegetation fires may be important...from soils becoming airborne by wind erosion...

Thomas A. J. Kuhlbusch

1998-06-19T23:59:59.000Z

405

Carbon Capture Research and Development  

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

Center Lawrence Berkeley National Laboratory Research Institute of Innovative Energy Carbon Capture Research and Development Carbon capture and storage from fossil-based power...

406

Carbon Trust | Open Energy Information  

Open Energy Info (EERE)

company funded by the UK government to help business and the public sector cut carbon emissions and capture the commercial potential of low carbon technologies....

407

Pacific Northwest rangeland carbon sequestration.  

E-Print Network [OSTI]

??This paper models the supply curve of carbon sequestration on Pacific Northwest rangelands. Rangeland managers have the ability to sequester carbon in agricultural soils by… (more)

Wiggins, Seth T.

2012-01-01T23:59:59.000Z

408

CARBON SEQUESTRATION STRATEGIES FOR CALIFORNIA  

E-Print Network [OSTI]

GEOLOGIC CARBON SEQUESTRATION STRATEGIES FOR CALIFORNIA: REPORT TO THE LEGISLATURE Regional Carbon Sequestration Partnership (WESTCARB) studies that we used, including Cameron Downey

409

Carbon nanotubes for organic electronics.  

E-Print Network [OSTI]

??This thesis investigated the use of carbon nanotubes as active components in solution processible organic semiconductor devices. We investigated the use of functionalized carbon nanotubes… (more)

Goh, Roland Ghim Siong

2008-01-01T23:59:59.000Z

410

Recovery of iron, carbon and zinc from steel plant waste oxides using the AISI-DOE postcombustion smelting technology  

SciTech Connect (OSTI)

This report describes a process to recover steel plant waste oxides to be used in the production of hot metal. The process flowsheet used at the pilot plant. Coal/coke breeze and iron ore pellets/waste oxides are charged into the smelting reactor. The waste oxides are either agglomerated into briquettes (1 inch) using a binder or micro-agglomerated into pellets (1/4 inch) without the use of a binder. The iron oxides dissolve in the slag and are reduced by carbon to produce molten iron. The gangue oxides present in the raw materials report to the slag. Coal charged to the smelter is both the fuel as well as the reductant. Carbon present in the waste oxides is also used as the fuel/reductant resulting in a decrease in the coal requirement. Oxygen is top blown through a central, water-cooled, dual circuit lance. Nitrogen is injected through tuyeres at the bottom of the reactor for stirring purposes. The hot metal and slag produced in the smelting reactor are tapped at regular intervals through a single taphole using a mudgun and drill system. The energy requirements of the process are provided by (i) the combustion of carbon to carbon monoxide, referred to as primary combustion and (ii) the combustion of CO and H{sub 2} to CO{sub 2} and H{sub 2}O, known as postcombustion.

Sarma, B. [Praxair, Inc., Tarrytown, NY (United States); Downing, K.B. [Fluor Daniel, Greenville, SC (United States); Aukrust, E.

1996-09-01T23:59:59.000Z

411

IMPACCT: Carbon Capture Technology  

SciTech Connect (OSTI)

IMPACCT Project: IMPACCT’s 15 projects seek to develop technologies for existing coal-fired power plants that will lower the cost of carbon capture. Short for “Innovative Materials and Processes for Advanced Carbon Capture Technologies,” the IMPACCT Project is geared toward minimizing the cost of removing carbon dioxide (CO2) from coal-fired power plant exhaust by developing materials and processes that have never before been considered for this application. Retrofitting coal-fired power plants to capture the CO2 they produce would enable greenhouse gas reductions without forcing these plants to close, shifting away from the inexpensive and abundant U.S. coal supply.

None

2012-01-01T23:59:59.000Z

412

Trading Water for Carbon with Biological Carbon Sequestration  

E-Print Network [OSTI]

Trading Water for Carbon with Biological Carbon Sequestration Robert B. Jackson,1 * Esteban G. Farley,1 David C. le Maitre,5 Bruce A. McCarl,6 Brian C. Murray7 Carbon sequestration strategies plantations feature prominently among tools for carbon sequestration (1­8). Plantations typi- cally combine

Nacional de San Luis, Universidad

413

Accelerated Carbonation of Brucite in Mine Tailings for Carbon Sequestration  

Science Journals Connector (OSTI)

Atmospheric CO2 is sequestered within ultramafic mine tailings via carbonation of Mg-bearing minerals. ... If carbonation of bulk tailings were accelerated, large mines may have the capacity to sequester millions of tonnes of CO2 annually, offsetting mine emissions. ... A Greenhouse-Scale Photosynthetic Microbial Bioreactor for Carbon Sequestration in Magnesium Carbonate Minerals ...

Anna L. Harrison; Ian M. Power; Gregory M. Dipple

2012-07-06T23:59:59.000Z

414

Cumulative Carbon and Just Allocation of the Global Carbon Commons  

E-Print Network [OSTI]

Cumulative Carbon and Just Allocation of the Global Carbon Commons R.T. Pierrehumbert* Abstract statistic, called cumulative carbon. This statistic is the aggregate amount ofcarbon emitted in theform such activitiespersist.In thispaper the conceptis usedto addressthe question offair allocation of carbon emissions

Pierrehumbert, Raymond

415

International Conference on Carbon Nanotechnology: Potential and Challenges (Carbon 10)  

E-Print Network [OSTI]

International Conference on Carbon Nanotechnology: Potential and Challenges (Carbon 10) 15 - 17th Since the discovery of the carbon nanotube (CNT) about two decades ago, research related to its of Materials and Process Engineering Kanpur Chapter hosted the `International Conference on Carbon

Srivastava, Kumar Vaibhav

416

Carbon nanotubes : synthesis, characterization, and applications  

E-Print Network [OSTI]

fibers, carbon nanotubes, and carbon capsule structures canand multi-walled nanotubes and carbon fiber, and occurs withMulti- walled carbon nanotubes”, Carbon, v.43, pp.2608-2617,

Deck, Christian Peter

2009-01-01T23:59:59.000Z

417

Carbon Dioxide Capture by Absorption with Potassium Carbonate  

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

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

418

Carbon Capture and Storage  

Science Journals Connector (OSTI)

The main object of the carbon capture and storage (CCS) technologies is the...2...emissions produced in the combustion of fossil fuels such as coal, oil, or natural gas. CCS involves first the capture of the emit...

Ricardo Guerrero-Lemus; José Manuel Martínez-Duart

2013-01-01T23:59:59.000Z

419

Introduction to Carbon Capture  

Science Journals Connector (OSTI)

Chapters 7–9 examine nontraditional separation technologies that in the most ideal sense may be considered carbon-neutral. The topics covered in these chapters include the role that algae plays in CO2 capture, CO

Prof. Jennifer Wilcox

2012-01-01T23:59:59.000Z

420

Low Carbon Fuel Standards  

E-Print Network [OSTI]

S O N I A YE H Low Carbon Fuel Standards The most direct andalternative transportation fuels is to spur innovation withstandard for upstream fuel producers. hen it comes to energy

Sperling, Dan; Yeh, Sonia

2009-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "hc carbon monoxide" 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

ATK - Supersonic Carbon Capture  

SciTech Connect (OSTI)

ATK and ACEnt Laboratories, with the help of ARPA-E funding, have taken an aerospace problem, supersonic condensation, and turned it into a viable clean energy solution for carbon capture.

Castrogiovanni, Anthony (ACEnT Laboratories, President and CEO) [ACEnT Laboratories, President and CEO; Calayag, Bon (ATK, Program Manager) [ATK, Program Manager

2014-03-05T23:59:59.000Z

422

Carbon Capture Pilots (Kentucky)  

Broader source: Energy.gov [DOE]

Support for the Carbon Management Research Group (CMRG), a public/private partnership consisting of most of the Commonwealth’s utilities, the Electric Power Research Institute, the Center for...

423

Wetland (peat) Carbon Cycle  

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

Wetland (peat) Carbon Cycle Methane (CH4) is an important greenhouse gas, twenty times more potent than CO2, but atmospheric concentrations of CH4 under future climate change are...

424

Research Summary Carbon Additionality  

E-Print Network [OSTI]

of the quality assurance of emissions reduction and carbon sequestration activities, but remains a source of much/reporting additionality rules. Technological Application of specific technology. Term Abatement arises within a specified

425

Method for synthesizing carbon nanotubes  

DOE Patents [OSTI]

A method for preparing a precursor solution for synthesis of carbon nanomaterials, where a polar solvent is added to at least one block copolymer and at least one carbohydrate compound, and the precursor solution is processed using a self-assembly process and subsequent heating to form nanoporous carbon films, porous carbon nanotubes, and porous carbon nanoparticles.

Fan, Hongyou

2012-09-04T23:59:59.000Z

426

4, 1367, 2007 Modelling carbon  

E-Print Network [OSTI]

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

Paris-Sud XI, Université de

427

Black Carbon’s Properties and Role in the Environment: A Comprehensive Review  

E-Print Network [OSTI]

H. Can reducing black carbon emissions counteract globalinventory of black carbon emissions. Atmos. Environ. 1993,commonly studied form of carbon emissions. Black carbon (BC)

Shrestha, Gyami

2010-01-01T23:59:59.000Z

428

The Development of a Hydrothermal Method for Slurry Feedstock Preparation for Gasification Technology  

E-Print Network [OSTI]

syngas (carbon monoxide and hydrogen) is produced instead of carbon dioxide and water as is in the combustion

He, Wei

2011-01-01T23:59:59.000Z

429

Study of fire retardant behavior of carbon nanotube membranes and carbon nanofiber paper in carbon fiber  

E-Print Network [OSTI]

were incorporated onto the surface of epoxy carbon fiber composites, as proposed fire shieldsStudy of fire retardant behavior of carbon nanotube membranes and carbon nanofiber paper in carbon fiber reinforced epoxy composites Qiang Wu, Wei Zhu, Chuck Zhang *, Zhiyong Liang, Ben Wang Department

Das, Suman

430

Measurement of carbon capture efficiency and stored carbon leakage  

DOE Patents [OSTI]

Data representative of a measured carbon dioxide (CO.sub.2) concentration and of a measured oxygen (O.sub.2) concentration at a measurement location can be used to determine whether the measured carbon dioxide concentration at the measurement location is elevated relative to a baseline carbon dioxide concentration due to escape of carbon dioxide from a source associated with a carbon capture and storage process. Optionally, the data can be used to quantify a carbon dioxide concentration increase at the first location that is attributable to escape of carbon dioxide from the source and to calculate a rate of escape of carbon dioxide from the source by executing a model of gas-phase transport using at least the first carbon dioxide concentration increase. Related systems, methods, and articles of manufacture are also described.

Keeling, Ralph F.; Dubey, Manvendra K.

2013-01-29T23:59:59.000Z

431

NETL: Carbon Storage - Big Sky Carbon Sequestration Partnership  

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

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

432

Chemically modified carbonic anhydrases useful in carbon capture systems  

SciTech Connect (OSTI)

The present disclosure relates to chemically modified carbonic anhydrase polypeptides and soluble compositions, homogenous liquid formulations comprising them. The chemically modified carbonic anhydrase polypeptides have improved properties relative to the same carbonic anhydrase polypeptide that is not chemically modified including the improved properties of increased activity and/or stability in the presence of amine compounds, ammonia, or carbonate ion. The present disclosure also provides methods of preparing the chemically modified polypeptides and methods of using the chemically modified polypeptides for accelerating the absorption of carbon dioxide from a gas stream into a solution as well as for the release of the absorbed carbon dioxide for further treatment and/or sequestering.

Novick, Scott; Alvizo, Oscar

2013-01-15T23:59:59.000Z

433

Chemically modified carbonic anhydrases useful in carbon capture systems  

DOE Patents [OSTI]

The present disclosure relates to chemically modified carbonic anhydrase polypeptides and soluble compositions, homogenous liquid formulations comprising them. The chemically modified carbonic anhydrase polypeptides have improved properties relative to the same carbonic anhydrase polypeptide that is not chemically modified including the improved properties of increased activity and/or stability in the presence of amine compounds, ammonia, or carbonate ion. The present disclosure also provides methods of preparing the chemically modified polypeptides and methods of using the chemically modified polypeptides for accelerating the absorption of carbon dioxide from a gas stream into a solution as well as for the release of the absorbed carbon dioxide for further treatment and/or sequestering.

Novick, Scott J; Alvizo, Oscar

2013-10-29T23:59:59.000Z

434

Effect of low steam/carbon ratio on water gas shift reaction  

Science Journals Connector (OSTI)

Cu/ZnO/Al2O3 catalysts prepared by reverse co-precipitation and an industrial catalyst were used for the low-temperature water gas shift reaction. The catalysts were characterized by chemical analysis (atomic absorption spectroscopy), BET surface area, nitrous oxide chemisorption, X-ray diffraction (XRD), temperature-programmed reduction (TPR), X-ray photoelectron spectroscopy (XPS) and catalytic activity in the target reaction. The catalyst prepared by reverse co-precipitation showed higher BET and copper surface areas, as well as higher catalytic activity. XRD patterns showed that the aurichalcite and hydrozincite precursors were converted into crystalline CuO and ZnO oxides when calcined in air at 623 K. TPR profiles revealed that Cu(I) oxide forms prior to Cu. Binding energies corresponding to several copper states on fresh catalysts were observed by XPS, but copper was in the metallic state during the reaction conditions (reduced catalyst). By varying the catalytic reaction conditions, such as vapor/carbon ratio and the time of contact, it is possible to obtain different conversion rates of carbon monoxide and thus operate under conditions of lower vapor consumption.

Renan Tavares Figueiredo; André Luis Dantas Ramos; Heloysa Martins Carvalho de Andrade; J.L.G. Fierro

2005-01-01T23:59:59.000Z

435

Method for converting hydrocarbon fuel into hydrogen gas and carbon dioxide  

DOE Patents [OSTI]

A method for converting hydrocarbon fuel into hydrogen gas and carbon dioxide within a reformer 10 is disclosed. According to the method, a stream including an oxygen-containing gas is directed adjacent to a first vessel 18 and the oxygen-containing gas is heated. A stream including unburned fuel is introduced into the oxygen-containing gas stream to form a mixture including oxygen-containing gas and fuel. The mixture of oxygen-containing gas and unburned fuel is directed tangentially into a partial oxidation reaction zone 24 within the first vessel 18. The mixture of oxygen-containing gas and fuel is further directed through the partial oxidation reaction zone 24 to produce a heated reformate stream including hydrogen gas and carbon monoxide. Steam may also be mixed with the oxygen-containing gas and fuel, and the reformate stream from the partial oxidation reaction zone 24 directed into a steam reforming zone 26. High- and low-temperature shift reaction zones 64,76 may be employed for further fuel processing.

Clawson, Lawrence G. (Dover, MA); Mitchell, William L. (Belmont, MA); Bentley, Jeffrey M. (Westford, MA); Thijssen, Johannes H. J. (Cambridge, MA)

2000-01-01T23:59:59.000Z

436

NETL: Carbon Dioxide 101 FAQs  

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

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

437

Carbon Trading Protocols for Geologic Sequestration  

E-Print Network [OSTI]

H. , 2005, IPCC: Carbon Capture and Storage: Technical05CH11231. INTRODUCTION Carbon capture and storage (CCS)Development Mechanism CCS: Carbon Capture and Storage C02e:

Hoversten, Shanna

2009-01-01T23:59:59.000Z

438

The Social Carbon Company | Open Energy Information  

Open Energy Info (EERE)

Carbon Company Jump to: navigation, search Name: The Social Carbon Company Place: Brasilia, Distrito Federal (Brasilia), Brazil Zip: CEP 70610-440 Sector: Carbon, Services Product:...

439

Carbon Nanohoops: Molecular Templates for Precision Nanotube...  

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

build carbon-ring "nanohoops," molecular building blocks for the formation of carbon nanotubes. Carbon nanohoops might serve as seeds, or templates, for the efficient and...

440

Electrochemical implications of defects in carbon nanotubes  

E-Print Network [OSTI]

in Hollow Carbon Nanotubes . . . . . . 4.3.2.1 IncreasingThe electrochemistry of carbon nanotubes. Journal of Thethe sidewalls of carbon nanotubes. Journal of the American

Hoefer, Mark

2012-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "hc carbon monoxide" 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

Thermal Management Using Carbon Nanotubes - Energy Innovation...  

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

Thermal Management Using Carbon Nanotubes Oak Ridge National Laboratory Contact ORNL About This Technology Vertically Aligned Carbon Nanotubes Vertically Aligned Carbon Nanotubes...

442

A cell nanoinjector based on carbon nanotubes  

E-Print Network [OSTI]

based on carbon nanotubes Xing Chen *|| , Andras Kis †|| ,that uses carbon nanotubes to deliver cargo into cells. Astrength (2, 3), carbon nanotubes (CNTs) are ideal nanoscale

Chen, Xing; Kis, Andras; Zettl, Alex; Bertozzi, Carolyn R.

2008-01-01T23:59:59.000Z

443

Electron transport through single carbon nanotubes  

E-Print Network [OSTI]

through single carbon nanotubes G. Chai Apollo Technologies,aligned multi-wall carbon nanotubes (CNT). Embedding of CNTsuse of fiber coated carbon nanotubes makes the handling of

Chai, G

2008-01-01T23:59:59.000Z

444

Ultrafast Nonlinear Spectroscopy of Semiconducting Carbon Nanotubes  

E-Print Network [OSTI]

Exciton binding energies in carbon nanotubes from two-photonExciton binding energies in carbon nanotubes from two-photonoptical transition energies of carbon nanotubes: the role of

Graham, Matthew Werden

2010-01-01T23:59:59.000Z

445

Equinox Carbon Equities LLC | Open Energy Information  

Open Energy Info (EERE)

Equities, LLC Place: Newport Beach, California Zip: 92660 Sector: Carbon Product: Investment firm focused on carbon trading References: Equinox Carbon Equities, LLC1 This...

446

Carbon Trust Investments Ltd | Open Energy Information  

Open Energy Info (EERE)

Ltd Place: United Kingdom Sector: Carbon Product: UK-based venture capital investment division of The Carbon Trust. References: Carbon Trust Investments Ltd1 This...

447

Carbon Nanotubes: Bearing Stress Like Never Before  

E-Print Network [OSTI]

Hart, A.J. (2013). Carbon Nanotubes: Present and Futureproduction of carbon nanotubes, and can be used to producesynthesized properly, and carbon nanotubes are no exception.

Limaye, Aditya

2013-01-01T23:59:59.000Z

448

Electrochemical implications of defects in carbon nanotubes  

E-Print Network [OSTI]

parameters. Fullerenes, Nanotubes and Carbon Nanostructures,in Hollow Carbon Nanotubes . . . . . . 4.3.2.1 Increasingmigration in graphite and carbon nanotubes. Chemical Physics

Hoefer, Mark

2012-01-01T23:59:59.000Z

449

Carbon Nanotube and Graphene Nanoelectromechanical Systems  

E-Print Network [OSTI]

Carbon Nanotubes on the2.4 Static Deformation of Carbon Nanotubes . . . . . .3.2 Field Emission from Carbon Nanotubes: Electrostatics

Aleman, Benjamin Jose

2011-01-01T23:59:59.000Z

450

Defects and Disorder in Carbon Nanotubes  

E-Print Network [OSTI]

Perebeinos, V. (2008) Carbon Nanotubes 111 423. Bachilo, S.M. & Mceuen, P. L. (2008) Carbon Nanotubes 111 Biro, L. P. ,sectional structure of carbon nanotubes. Fullerenes '96.

Collins, Philip G

2010-01-01T23:59:59.000Z

451

Electron transport through single carbon nanotubes  

E-Print Network [OSTI]

transport through single carbon nanotubes G. Chai Apolloaligned multi-wall carbon nanotubes (CNT). Embedding of CNTsuse of fiber coated carbon nanotubes makes the handling of

Chai, G

2008-01-01T23:59:59.000Z

452

How Carbon Capture Works | Department of Energy  

Energy Savers [EERE]

past two decades. Carbon capture, utilization and storage (CCUS) -- also referred to as carbon capture, utilization and sequestration -- is a process that captures carbon dioxide...

453

Participatory Carbon Monitoring: Operational Guidance for National...  

Open Energy Info (EERE)

Participatory Carbon Monitoring: Operational Guidance for National REDD+ Carbon Accounting Jump to: navigation, search Tool Summary LAUNCH TOOL Name: Participatory Carbon...

454

Universal Carbon Credits Limited | Open Energy Information  

Open Energy Info (EERE)

Universal Carbon Credits Limited Jump to: navigation, search Name: Universal Carbon Credits Limited Place: London, England, United Kingdom Zip: EC3A6DF Sector: Carbon Product:...

455

Carbon nanotubes : synthesis, characterization, and applications  

E-Print Network [OSTI]

around Surface-Attached Carbon Nanotubes. Ind. Eng. Chem.the flexural rigidity of carbon nanotube ensembles. AppliedNanotechnology in Carbon Materials. Acta Metallurgica, 1997.

Deck, Christian Peter

2009-01-01T23:59:59.000Z

456

Distributed Energy Resources for Carbon Emissions Mitigation  

E-Print Network [OSTI]

Energy Resources for Carbon Emissions Mitigation RyanEnergy Resources for Carbon Emissions Mitigation Ryanand/or site-attributable carbon emissions at commercial and

Firestone, Ryan; Marnay, Chris

2008-01-01T23:59:59.000Z

457

GS Carbon Corporation | Open Energy Information  

Open Energy Info (EERE)

search Name: GS Carbon Corporation Place: New York, New York Zip: 10119 Sector: Carbon Product: The company offsets emissions output with carbon credits through the...

458

BNL | Carbon Cycle Science  

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

The Carbon Cycle Science & Technology Group aims to increase understanding The Carbon Cycle Science & Technology Group aims to increase understanding of the impacts of global change on managed and unmanaged ecosystems and improve knowledge of possible global change mitigation approaches. The group has three main focus areas. FACE Climate Change Experimental Facility Design and Management The CCS&T group is an internationally recognized leader in the development of Free Air CO2 Enrichment (FACE) research facilities. We are interested in the design and management of manipulative experiments that examine the effects of carbon dioxide, ozone, other atmospheric pollutants, temperature and precipitation on natural and managed ecosystems. FACE Plant Physiology and High Throughput Biochemical Phenotyping At FACE facilities we have studied the mechanisms that underlie the

459

Carbon Sequestration 101  

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

Perspectives on Carbon Capture and Storage Perspectives on Carbon Capture and Storage - Directions, Challenges, and Opportunities Thomas J. Feeley, III National Energy Technology Laboratory Carbon Capture and Storage November 13-15, 2007 Austin, Texas C Capture & Storage, Austin, TX Nov. 13-15, 2007 U.S. Fossil Fuel Reserves / Production Ratio 250+ Year Supply at Current Demand Levels ! 258 11.7 9.7 0 100 200 300 Coal Oil Natural Gas Anthracite & Bituminous Sub- Bituminous & Lignite Sources: BP Statistical Review, June 2004, - for coal reserves data - World Energy Council; EIA, Advance Summary U.S. Crude Oil, Natural Gas, and Natural Gas Liquids Reserves, 2003 Annual Report, September 22, 2004 - for oil and gas reserves data. C Capture & Storage, Austin, TX Nov. 13-15, 2007 80 120 160 200 240 1970 1975 1980

460

Carbon Storage Review 2012  

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

Sequestration Options in the Illinois Basin - Phase III DE-FC26-05NT42588 Robert J. Finley and the MGSC Project Team Illinois State Geological Survey (University of Illinois) and Schlumberger Carbon Services U.S. Department of Energy National Energy Technology Laboratory Carbon Storage R&D Project Review Meeting Developing the Technologies and Building the Infrastructure for CO 2 Storage August 21-23, 2012 * The Midwest Geological Sequestration Consortium is funded by the U.S. Department of Energy through the National Energy Technology Laboratory (NETL) via the Regional Carbon Sequestration Partnership Program (contract number DE-FC26-05NT42588) and by a cost share agreement with the Illinois Department of Commerce and Economic Opportunity, Office of Coal Development through the Illinois Clean Coal

Note: This page contains sample records for the topic "hc carbon monoxide" 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

RMOTC - Testing - Carbon Management  

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

Carbon Management Carbon Management Ten Sleep Time Structure, 2nd Wall Creek Formation at RMOTC Notice: As of July 15th 2013, the Department of Energy announced the intent to sell Naval Petroleum Reserve Number 3 (NPR3). The sale of NPR-3 will also include the sale of all equipment and materials onsite. A decision has been made by the Department of Energy to complete testing at RMOTC by July 1st, 2014. RMOTC will complete testing in the coming year with the currently scheduled testing partners. For more information on the sale of NPR-3 and sale of RMOTC equipment and materials please join our mailing list here. RMOTC has the field setting, infrastructure, and expertise to play an important role in carbon management testing, demonstration, and research. The unique combination of a publicly-owned and DOE-operated oil field,

462

Success Stories: Carbon Explorer  

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

LBNL Device Monitors Ocean Carbon LBNL Device Monitors Ocean Carbon Imagine waking up each morning and discovering that twenty percent of all plants in your garden had disappeared over night. They had been eaten. Equally astonishing would be the discovery in the afternoon that new plants had taken their place. This is the norm of life in the ocean. Without the ability to accurately observe these daily changes in ocean life cycles, over vast spatial scales, we lack the ability to predict how the ocean will respond to rising CO2 levels, crippling our ability to develop accurate models of global warming or devise strategies to prevent it. The Carbon Explorer, conceived by Berkeley Lab's James K. Bishop in collaboration with Scripps Institution of Oceanography (La Jolla, California) and WET labs, Inc. (Philomath, Oregon), bridges this

463

Carbon Materials Breakout Group  

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

Materials Breakout Group Process Materials Breakout Group Process * Day 2, Thursday - Review results of Day 1 and modify if needed - Identify critical R&D needs - Outline R&D plan with key milestones - Report results to plenary Carbon Materials Breakout Group * Key Results - Target: get the science right to engineer carbon materials for hydrogen storage * Integrate theory, experiment, engineering * Understand mechanisms, effects, and interactions ranging from physisorption to chemisorption - Theory * Provide "directional" guidance for experiments (and vice- versa) * Provide baseline theory to elucidate parameters affecting the number and type of binding sites and the heat of their interaction with H2 (∆H ) for a broad range of (highly) modified carbon materials

464

Authigenic Carbonate and the History of the Global Carbon Cycle  

Science Journals Connector (OSTI)

...Earth's surface reservoirs ({delta} 13 C...of carbonate rocks. In either case, this...history when the porosity and permeability of...track the bulk rock {delta} 13...of carbonate rocks...sedimentary reservoirs does...

Daniel P. Schrag; John. A. Higgins; Francis A. Macdonald; David T. Johnston

2013-02-01T23:59:59.000Z

465

Development of carbon-carbon composites from solvent extracted pitch  

SciTech Connect (OSTI)

There are several methods used to fabricate carbon-carbon composites. One used extensively in the fabrication of aerospace components such as rocket nozzles and reentry vehicle nosetips, as well as commercial components for furnace fixturing and glass manufacturing, is the densification of a woven preform with molten pitch, and the subsequent conversion of the pitch to graphite through heat treatment. Two types of pitch are used in this process; coal tar pitch and petroleum pitch. The objective of this program was to determine if a pitch produced by the direct extraction of coal could be used as a substitute for these pitches in the fabrication of carbon-carbon composites. The program involved comparing solvent extracted pitch with currently accepted pitches and rigidizing a carbon-carbon preform with solvent extracted pitch for comparison with carbon-carbon fabricated with currently available pitch.

NONE

1996-06-24T23:59:59.000Z

466

Carbon Capture and Storage  

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

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

467

Carbon Capture and Storage  

SciTech Connect (OSTI)

Carbon capture and sequestration (CCS) is the long-term isolation of carbon dioxide from the atmosphere through physical, chemical, biological, or engineered processes. This includes a range of approaches including soil carbon sequestration (e.g., through no-till farming), terrestrial biomass sequestration (e.g., through planting forests), direct ocean injection of CO{sub 2} either onto the deep seafloor or into the intermediate depths, injection into deep geological formations, or even direct conversion of CO{sub 2} to carbonate minerals. Some of these approaches are considered geoengineering (see the appropriate chapter herein). All are considered in the 2005 special report by the Intergovernmental Panel on Climate Change (IPCC 2005). Of the range of options available, geological carbon sequestration (GCS) appears to be the most actionable and economic option for major greenhouse gas reduction in the next 10-30 years. The basis for this interest includes several factors: (1) The potential capacities are large based on initial estimates. Formal estimates for global storage potential vary substantially, but are likely to be between 800 and 3300 Gt of C (3000 and 10,000 Gt of CO{sub 2}), with significant capacity located reasonably near large point sources of the CO{sub 2}. (2) GCS can begin operations with demonstrated technology. Carbon dioxide has been separated from large point sources for nearly 100 years, and has been injected underground for over 30 years (below). (3) Testing of GCS at intermediate scale is feasible. In the US, Canada, and many industrial countries, large CO{sub 2} sources like power plants and refineries lie near prospective storage sites. These plants could be retrofit today and injection begun (while bearing in mind scientific uncertainties and unknowns). Indeed, some have, and three projects described here provide a great deal of information on the operational needs and field implementation of CCS. Part of this interest comes from several key documents written in the last three years that provide information on the status, economics, technology, and impact of CCS. These are cited throughout this text and identified as key references at the end of this manuscript. When coupled with improvements in energy efficiency, renewable energy supplies, and nuclear power, CCS help dramatically reduce current and future emissions (US CCTP 2005, MIT 2007). If CCS is not available as a carbon management option, it will be much more difficult and much more expensive to stabilize atmospheric CO{sub 2} emissions. Recent estimates put the cost of carbon abatement without CCS to be 30-80% higher that if CCS were to be available (Edmonds et al. 2004).

Friedmann, S

2007-10-03T23:59:59.000Z

468

Low Cost Carbon Fiber Production Carbon Fiber Manufacturing Cost Modeling  

E-Print Network [OSTI]

Low Cost Carbon Fiber Production Carbon Fiber Manufacturing Cost Modeling Oak Ridge National fiber reinforced composites have enjoyed limited acceptance in the automotive industry due to high costs to bond with composite matrix material. It is important that a carbon fiber manufacturing cost model

469

ISSUES IN EVALUATING CARBON SEQUESTRATION AND ATTRIBUTING CARBON CREDITS TO GRASSLAND RESTORATION EFFORTS  

E-Print Network [OSTI]

ISSUES IN EVALUATING CARBON SEQUESTRATION AND ATTRIBUTING CARBON CREDITS TO GRASSLAND RESTORATION examines biological carbon sequestration using a grassland restoration as a model system. Chapter 1 for biological carbon sequestration. In this analysis, we found that significantly greater soil carbon

Wisconsin at Madison, University of

470

Carbon Jungle | Open Energy Information  

Open Energy Info (EERE)

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

471

Organic modification of carbon nanotubes  

Science Journals Connector (OSTI)

The organic modification of carbon nanotubes is a novel research field being developed ... and newest progress of organic modification of carbon nanotubes are reviewed from two aspects: organic covalent modificat...

Luqi Liu; Zhixin Guo; Liming Dai; Daoben Zhu

2002-03-01T23:59:59.000Z

472

Irradiation Stability of Carbon Nanotubes  

E-Print Network [OSTI]

Ion irradiation of carbon nanotubes is a tool that can be used to achieve modification of the structure. Irradiation stability of carbon nanotubes was studied by ion and electron bombardment of the samples. Different ion species at various energies...

Aitkaliyeva, Assel

2010-01-14T23:59:59.000Z

473

Asset Carbon | Open Energy Information  

Open Energy Info (EERE)

Carbon Place: United Kingdom Product: UK-based startup looking to invest in CDMJI projects. References: Asset Carbon1 This article is a stub. You can help OpenEI by expanding...

474

Forests, carbon and global climate  

Science Journals Connector (OSTI)

...through fossil-fuel combustion and land-use change...Atmosphere analysis Biomass Carbon metabolism Carbon...through fossil-fuel combustion and land-use change...during fossil fuel and biomass combustion and the release of ammo...

2002-01-01T23:59:59.000Z

475

Carbon smackdown: wind warriors  

ScienceCinema (OSTI)

July 16. 2010 carbon smackdown summer lecture: learn how Berkeley Lab scientists are developing wind turbines to be used in an urban setting, as well as analyzing what it will take to increase the adoption of wind energy in the U.S.

Glen Dahlbacka of the Accelerator & Fusion Research Division and Ryan Wiser of the Environmental Energy Technologies Division are the speakers.

2010-09-01T23:59:59.000Z

476

Carbon-Fuelled Future  

SciTech Connect (OSTI)

Whether due to changes in policy or consumption of available fossil fuels, alternative sources of energy will be required, especially given the rising global energy demand. However, one of the main factors limiting the widespread utilization of renewable energy, such as wind, solar, wave or geothermal, is our ability to store energy. Storage of energy from carbon-neutral sources, such as electricity from solar or wind, can be accomplished through many routes. One approach is to store energy in the form of chemical bonds, as fuels. The conversion of low-energy compounds, such as water and carbon dioxide, to higher energy molecules, such as hydrogen or carbon-based fuels, enables the storage of carbon-neutral energy on a very large scale. The author¹s work in this area is supported by the US Department of Energy Basic Energy Sciences, Division of Chemical Sciences, Geosciences & Biosciences. Pacific Northwest National Laboratory is operated by Battelle for the US Department of Energy.

Appel, Aaron M.

2014-09-12T23:59:59.000Z

477

CARBON DIOXIDE EMISSION REDUCTION  

E-Print Network [OSTI]

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

Delaware, University of

478

Carbon Footprint Calculator  

Broader source: Energy.gov [DOE]

This calculator estimates the amount of carbon emissions you and members of your household are responsible for. It does not include emissions associated with your work or getting to work if you commute by public transportation. It was developed by IEEE Spectrum magazine.

479

decommissioning of carbon dioxide (CO  

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

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

480

Less Carbon Ltd | Open Energy Information  

Open Energy Info (EERE)

Less Carbon Ltd Jump to: navigation, search Name: Less Carbon Ltd Place: London, Greater London, United Kingdom Zip: EC3M 4BT Sector: Carbon Product: Less Carbon advises energy...

Note: This page contains sample records for the topic "hc carbon monoxide" 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

First Carbon Fund Ltd | Open Energy Information  

Open Energy Info (EERE)

First Carbon Fund Ltd Jump to: navigation, search Name: First Carbon Fund Ltd Place: London, Greater London, United Kingdom Zip: EC1V 9EE Sector: Carbon Product: First Carbon Fund...

482

The development and deployment of a ground-based, laser-induced fluorescence instrument for the in situ detection of iodine monoxide radicals  

SciTech Connect (OSTI)

High abundances of iodine monoxide (IO) are known to exist and to participate in local photochemistry of the marine boundary layer. Of particular interest are the roles IO plays in the formation of new particles in coastal marine environments and in depletion episodes of ozone and mercury in the Arctic polar spring. This paper describes a ground-based instrument that measures IO at mixing ratios less than one part in 10{sup 12}. The IO radical is measured by detecting laser-induced fluorescence at wavelengths longer that 500 nm. Tunable visible light is used to pump the A{sup 2}?{sub 3/2} (v{sup ?} = 2) ? X{sup 2}?{sub 3/2} (v{sup ?} = 0) transition of IO near 445 nm. The laser light is produced by a solid-state, Nd:YAG-pumped Ti:Sapphire laser at 5 kHz repetition rate. The laser-induced fluorescence instrument performs reliably with very high signal-to-noise ratios (>10) achieved in short integration times (<1 min). The observations from a validation deployment to the Shoals Marine Lab on Appledore Island, ME are presented and are broadly consistent with in situ observations from European Coastal Sites. Mixing ratios ranged from the instrumental detection limit (<1 pptv) to 10 pptv. These data represent the first in situ point measurements of IO in North America.

Thurlow, M. E., E-mail: thurlow@huarp.harvard.edu; Hannun, R. A.; Lapson, L. B.; Anderson, J. G. [Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138 (United States)] [Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138 (United States); Co, D. T. [Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138 (United States) [Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138 (United States); Argonne-Northwestern Solar Energy Research Center and Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208-3113 (United States); O'Brien, A. S. [Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138 (United States) [Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138 (United States); Department of Civil and Environmental Engineering, Princeton University, Princeton, New Jersey 08544 (United States); Hanisco, T. F. [Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138 (United States) [Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, Massachusetts 02138 (United States); NASA Goddard Space Flight Center, Code 614, Greenbelt, Maryland 20771 (United States)

2014-04-15T23:59:59.000Z

483

NETL: Gasifipedia - Carbon Sequestration  

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

Coal: SNG from Coal: Process & Commercialization: Carbon Sequestration Coal: SNG from Coal: Process & Commercialization: Carbon Sequestration Carbon sequestration, also termed carbon storage, is the permanent storage of CO2, usually in deep geologic formations. Industrially-generated CO2 -- resulting from fossil fuel combustion, gasification, and other industrial processes -- is injected as a supercritical fluid into geologic reservoirs, where it is held in place by natural traps and seals. Carbon storage is one approach to minimizing atmospheric emissions of man-made CO2. As discussed above, the main purpose of CO2 EOR such as the Weyburn Project is tertiary recovery of crude oil, but in effect substantial CO2 remains sequestered/stored as a result. Current Status of CO2 Storage CO2 storage is currently underway in the United States and around the world. Large, commercial-scale projects, like the Sleipner CO2 Storage Site in Norway and the Weyburn-Midale CO2 Project in Canada, have been injecting CO2 into geologic storage formations more than a decade. Each of these projects stores more than 1 million tons of CO2 per year. Large-scale efforts are currently underway in Africa, China, Australia, and Europe, as well. These commercial-scale projects are demonstrating that large volumes of CO2 can be safely and permanently stored. In addition, a number of smaller pilot projects are underway in different parts of the world to determine suitable locations and technologies for future long-term CO2 storage. To date, more than 200 small-scale CO2 storage projects have been carried out worldwide. A demonstration project that captures CO2 from a pulverized coal power plant and pipes it to a geologic formation for storage recently came online in Alabama.

484

Carbon Nanotubes for Data Processing  

E-Print Network [OSTI]

Carbon Nanotubes for Data Processing Joerg Appenzeller, T. J. Watson Research Center, IBM Research.2 Electronic Structure of Graphene 4 2.3 Electronic Structure of Carbon Nanotubes 4 2.4 Transport Properties 6 2.5 Contacts 9 3 Synthesis of Carbon Nanotubes 10 3.1 Synthetic Methods 10 3.2 Growth Mechanisms 12

Joselevich, Ernesto

485

4, 99123, 2007 Amazon carbon  

E-Print Network [OSTI]

, suggested much larger estimates for tropical forest carbon sequestration in the Ama- zon BasinBGD 4, 99­123, 2007 Amazon carbon balanc J. Lloyd et al. Title Page Abstract Introduction Discussions is the access reviewed discussion forum of Biogeosciences An airborne regional carbon balance

Boyer, Edmond

486

Dispersion toughened silicon carbon ceramics  

DOE Patents [OSTI]

Fracture resistant silicon carbide ceramics are provided by incorporating therein a particulate dispersoid selected from the group consisting of (a) a mixture of boron, carbon and tungsten, (b) a mixture of boron, carbon and molybdenum, (c) a mixture of boron, carbon and titanium carbide, (d) a mixture of aluminum oxide and zirconium oxide, and (e) boron nitride. 4 figures.

Wei, G.C.

1984-01-01T23:59:59.000Z

487

CARBON NANOTUBE TRANSISTORS: AN EVALUATION  

E-Print Network [OSTI]

CARBON NANOTUBE TRANSISTORS: AN EVALUATION L.C. Castro, D.L. John, and D.L. Pulfrey Department A simple, non-equilibrium model is used to evaluate the likely DC performance of carbon nanotube field and transcon- ductance close to the low-quantum-capacitance limit. Keywords: Carbon nanotubes, field

Pulfrey, David L.

488

1, 167193, 2004 Terrestrial carbon  

E-Print Network [OSTI]

BGD 1, 167­193, 2004 Terrestrial carbon budget at country-scale I. A. Janssens et al. Title Page Biogeosciences Discussions is the access reviewed discussion forum of Biogeosciences The carbon budget.janssens@ua.ac.be) 167 #12;BGD 1, 167­193, 2004 Terrestrial carbon budget at country-scale I. A. Janssens et al. Title

Paris-Sud XI, Université de

489

NETL: Carbon Storage - Southeast Regional Carbon Sequestration Partnership  

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

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

490

Hydrogen storage in multilayer carbon nanotubes  

Science Journals Connector (OSTI)

Multilayer carbon nanotubes obtained by pyrolysis and mechanical activation of plant-derived amorphous carbon are excellent sorbents for hydrogen.

D. V. Onishchenko; V. P. Reva; V. G. Kuryavyi

2013-05-01T23:59:59.000Z

491

Net carbon flux from agriculture: Carbon emissions, carbon sequestration, crop yield, and land-use change  

Science Journals Connector (OSTI)

There is a potential to sequester carbon in soil by changing agricultural management practices. ... fossil-fuel use, agricultural inputs, and the carbon emissions associated with fossil fuels and other ... with f...

Tristram O. West; Gregg Marland

2003-04-01T23:59:59.000Z

492

Carbon Sequestered, Carbon Displaced and the Kyoto Context  

SciTech Connect (OSTI)

The integrated system that embraces forest management, forest products, and land-use change impacts the global carbon cycle - and hence the net emission of the greenhouse gas carbon dioxide - in four fundamental ways. Carbon is stored in living and dead biomass, carbon is stored in wood products and landfills, forest products substitute in the market place for products made from other materials, and forest harvests can be used wholly or partially to displace fossil fuels in the energy sector. Implementation of the Kyoto Protocol to the United Nations Framework Convention on Climate Change would result in the creation of international markets for carbon dioxide emissions credits, but the current Kyoto text does not treat all carbon identically. We have developed a carbon accounting model, GORCAM, to examine a variety of scenarios for land management and the production of forest products. In this paper we explore, for two simple scenarios of forest management, the carbon flows that occur and how these might be accounted for under the Kyoto text. The Kyoto protocol raises questions about what activities can result in emissions credits, which carbon reservoirs will be counted, who will receive the credits, and how much credit will be available? The Kyoto Protocol would sometimes give credits for carbon sequestered, but it would always give credits when fossil-fuel carbon dioxide emissions are displaced.

Marland, G.; Schlamadinger, B.

1999-04-18T23:59:59.000Z

493

Highlights | The Ames Laboratory  

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

valuable H2, while the other removes an atom of carbon and oxygen and produces carbon monoxide. Typically carbon monoxide inhibits the removal of hydrogen, but the use of...

494

*** How PAN based Carbon Fibers are  

E-Print Network [OSTI]

*** How PAN based Carbon Fibers are Manufactured *** How Carbon Fiber Material Properties are Achieved *** Carbon Fiber Markets/Applications CarbonFiber AerospaceEngineeringGuestLecture: Friday as a Business Development Manager for Amoco's carbon fiber business unit (manufacturers of T-300 carbon fiber

Hu, Hui

495

6, 34193463, 2006 Black carbon or  

E-Print Network [OSTI]

ACPD 6, 3419­3463, 2006 Black carbon or brown carbon M. O. Andreae and A. Gelencs´er Title Page Chemistry and Physics Discussions Black carbon or brown carbon? The nature of light-absorbing carbonaceous;ACPD 6, 3419­3463, 2006 Black carbon or brown carbon M. O. Andreae and A. Gelencs´er Title Page

Paris-Sud XI, Université de

496

Carbon Cycle 2.0  

Broader source: Energy.gov (indexed) [DOE]

Carbon Cycle 2.0 Carbon Cycle 2.0 Pioneering science for sustainable energy solutions Artificial Photosynthesis Energy Storage Combustion Carbon Capture & Storage Developing World Efficiency Photovoltaics Biofuels Energy Analysis Climate Modeling Carbon Cycle 2.0 is... 1. A vision for * a global energy system integrated with the Earth's natural carbon cycles * an interactive Berkeley Lab environment with a shared sense of purpose 2. A program development plan that will allow us to deepen our capabilities and provide more opportunities to have impact 3. An attempt to integrate our basic research with applications using models of technology deployment constraints 4. Set of internal activities aimed at priming the effort

497

CHARTER FOR THE CARBON SEQUESTRATION  

Broader source: Energy.gov (indexed) [DOE]

CHARTER FOR THE CARBON SEQUESTRATION CHARTER FOR THE CARBON SEQUESTRATION LEADERSHIP FORUM (CSLF): A CARBON CAPTURE AND STORAGE TECHNOLOGY INITIATIVE The undersigned national governmental entities (collectively the "Members") set forth the following Terms of Reference for the Carbon Sequestration Leadership Forum (CSLF), a framework for international cooperation in research and development for the separation, capture, transportation and storage of carbon dioxide. The CSLF will seek to realize the promise of carbon capture and storage over the coming decades, making it commercially competitive and environmentally safe. 1. Purpose of the CSLF To facilitate the development of improved cost-effective technologies for the separation and capture of carbon dioxide for its transport and long-term safe storage; to make these

498

CARBON7510.pdf  

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

Author's personal copy Author's personal copy NMR a critical tool to study the production of carbon fiber from lignin Marcus Foston a , Grady A. Nunnery b , Xianzhi Meng a , Qining Sun a , Frederick S. Baker b , Arthur Ragauskas a, * a BioEnergy Science Center, School of Chemistry and Biochemistry, Institute of Paper Science and Technology, Georgia Institute of Technology, 500 10th St., Atlanta, GA 30332, United States b Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN 37831-6087, United States A R T I C L E I N F O Article history: Received 7 April 2012 Accepted 6 September 2012 Available online 14 September 2012 A B S T R A C T The structural changes occurring to hardwood Alcell TM lignin as a result of fiber devolatiliza- tion/extrusion, oxidative thermo-stabilization and carbonization are investigated in this study by solid-state and solution nuclear magnetic resonance

499

Magnetoconductance of carbon nanotubes  

Science Journals Connector (OSTI)

As a result of the interaction between the spin and the magnetic field (B), special step structures are predicted to exist in the ballistic magnetoconductance of carbon nanotubes. The electronic structure of a carbon nanotube drastically changes from a metal (semiconductor) to a semiconductor (metal) during the variation of the magnetic flux. When the spin-B interaction is neglected, the Fermi level only touches the conductance and valence bands of a metallic nanotube. This paramagnetic interaction could make the subbands cross and intersect with the Fermi level within a certain magnetic-flux range; the ballistic magnetoconductance thus exhibits step structures. Such special structures are expected to be observable at low temperature (<1 K) and bias voltage (<0.1 mV). Moreover there exists another effect, the doping effect, which could lead to step structures even without the spin-B interaction.

M. F. Lin and Kenneth W. -K. Shung

1995-03-15T23:59:59.000Z

500

Magnetism of carbon clusters  

Science Journals Connector (OSTI)

The ?-electron ring current magnetic susceptibilities and endohedral chemical shifts of the fullerenes are calculated with the London theory. The diamagnetism calculated for the fullerenes that have been characterized to date does not show a monotonic increase toward the graphite value. By carrying out calculations on high-symmetry giant fullerenes (Cn) in the size regime 100magnetic susceptibility of graphite on a per carbon basis. Endohedral chemical shifts are predicted to be invariant to cluster size, but subject to the quantum size effects seen in smaller fullerenes and metallic clusters. The fullerenes are different from the metallic clusters because the finite band gap in conjugated carbon compounds allows the diamagnetic term to dominate at large cluster size. The experimentally observed decrease in nanotube material diamagnetism with temperature is attributed to the increased importance of the Van Vleck term due to finite-temperature effects.

R. C. Haddon and Alfredo Pasquarello

1994-12-01T23:59:59.000Z