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Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

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...

2

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...

3

Composite catalyst for carbon monoxide and hydrocarbon oxidation  

DOE Patents [OSTI]

A method and composition for the complete oxidation of carbon monoxide and/or hydrocarbon compounds. The method involves reacting the carbon monoxide and/or hydrocarbons with an oxidizing agent in the presence of a metal oxide composite catalyst. The catalyst is prepared by combining fluorite-type oxygen ion conductors with active transition metals. The fluorite oxide, selected from the group consisting of cerium oxide, zirconium oxide, thorium oxide, hafnium oxide, and uranium oxide, and may be doped by alkaline earth and rare earth oxides. The transition metals, selected from the group consisting of molybdnum, copper, cobalt, maganese, nickel, and silver, are used as additives. The atomic ratio of transition metal to fluorite oxide is less than one.

Liu, Wei (Cambridge, MA); Flytzani-Stephanopoulos, Maria (Winchester, MA)

1996-01-01T23:59:59.000Z

4

Composite catalyst for carbon monoxide and hydrocarbon oxidation  

DOE Patents [OSTI]

A method and composition are disclosed for the complete oxidation of carbon monoxide and/or hydrocarbon compounds. The method involves reacting the carbon monoxide and/or hydrocarbons with an oxidizing agent in the presence of a metal oxide composite catalyst. The catalyst is prepared by combining fluorite-type oxygen ion conductors with active transition metals. The fluorite oxide, selected from the group consisting of cerium oxide, zirconium oxide, thorium oxide, hafnium oxide, and uranium oxide, and may be doped by alkaline earth and rare earth oxides. The transition metals, selected from the group consisting of molybdenum, copper, cobalt, manganese, nickel, and silver, are used as additives. The atomic ratio of transition metal to fluorite oxide is less than one.

Liu, W.; Flytzani-Stephanopoulos, M.

1996-03-19T23:59:59.000Z

5

Thermal device and method for production of carbon monoxide and hydrogen by thermal dissociation of hydrocarbon gases  

DOE Patents [OSTI]

Carbon monoxide is produced in a fast quench reactor. The production of carbon monoxide includes injecting carbon dioxide and some air into a reactor chamber having a high temperature at its inlet and a rapidly expanding a reactant stream, such as a restrictive convergent-divergent nozzle at its outlet end. Carbon dioxide and other reactants such as methane and other low molecular weight hydrocarbons are injected into the reactor chamber. Other gas may be added at different stages in the process to form a desired end product and prevent back reactions. The resulting heated gaseous stream is then rapidly cooled by expansion of the gaseous stream.

Detering, Brent A. (Idaho Falls, ID); Kong, Peter C. (Idaho Falls, ID)

2001-01-01T23:59:59.000Z

6

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

7

Prediction of Carbon Monoxide and Hydrocarbon Emissions in Isooctane HCCI Engine Combustion Using Multi-Zone Simulations  

SciTech Connect (OSTI)

Homogeneous Charge Compression Ignitions (HCCI) engines show promise as an alternative to Diesel engines, yet research remains: development of practical HCCI engines will be aided greatly by accurate modeling tools. A novel detailed chemical kinetic model that incorporates information from a computational fluid mechanics code has been developed to simulate HCCI combustion. This model very accurately predicts many aspects of the HCCI combustion process. High-resolution computational grids can be used for the fluid mechanics portion of the simulation, but the chemical kinetics portion of the simulation can be reduced to a handful of computational zones (for all previous work 10 zones have been used). While overall this model has demonstrated a very good predictive capability for HCCI combustion, previous simulations using this model have tended to underpredict carbon monoxide emissions by an order of magnitude. A factor in the underprediction of carbon monoxide may be that all previous simulations have been conducted with 10 chemical kinetic zones. The chemistry that results in carbon monoxide emissions is very sensitive to small changes in temperature within the engine. The resolution in temperature is determined directly by the number of zones. This paper investigates how the number of zones (i.e. temperature resolution) affects the model's prediction of hydrocarbon and carbon monoxide emissions in an HCCI engine. Simulations with 10, 20, and 40 chemical kinetic zones have been conducted using a detailed chemical kinetic mechanism (859 species, 3606 reactions) to simulate an isooctane fueled HCCI engine. The results show that 10-zones are adequate to resolve the hydrocarbon emissions, but a greater numbers of zones are required to resolve carbon monoxide emissions. Results are also presented that explore spatial sources of the exhaust emissions within the HCCI engine combustion chamber.

Flowers, D; Aceves, S M; Martinez-Frias, J; Dibble, R

2002-05-02T23:59:59.000Z

8

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

9

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

10

Carbon Monoxide, Ozone, Hydrocarbon Air Quality Standards, and Related Emission Requirements (Ohio)  

Broader source: Energy.gov [DOE]

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.

11

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

12

Hydrocarbon Observations and Ozone Production Rates in Western Houston During the Texas 2000 Air Quality Study  

SciTech Connect (OSTI)

Measurements of total non-methane hydrocarbon in whole air canisters collected from the top of a skyscraper on the western edge of Houston, Texas are summarized with an emphasis on samples collected during the passage of plumes of O{sub 3} and the associated rapid increase in the mixing ratio of this species. The back-trajectories associated with these events showed a pronounced deceleration of air parcels over central and western Houston and were not necessarily associated with direct passage over the petrochemical plants located in the heavily industrialized eastern part of Houston. As a result of the time these air parcels spent over the central and western parts of Houston, their VOC mix and associated chemical production rates were expected to differ from similar observations made over eastern Houston from aircraft sampling at low altitudes. Although periods of high O{sub 3} in the western part of the city were closely associated with light alkenes, these same observations show isoprene to make a significant contribution to the total VOC reactivity in the early afternoon (the start of peak photochemical activity) in contrast to observations made east of our sampling site that found the reactivity to be dominated by anthropogenic species. By initializing a 0-dimensional chemical kinetic model with observations made at the Williams Tower, we find that the ozone production efficiency scaled linearly to the ratio of total hydrocarbons and NO{sub x}, with an average OPE of 7.2, ranging from 2.3 to 16.9; these values are smaller than those reported in eastern Houston, suggesting a strong gradient in photochemical productivity across the city.

Berkowitz, Carl M.; Spicer, Chet W.; Doskey, Paul V.

2005-06-01T23:59:59.000Z

13

E-Print Network 3.0 - aromatic hydrocarbons methyl Sample Search...  

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

Renewable Energy 2 Quantification of Local Ozone Production Attributable to Automobile Hydrocarbon Emissions Summary: -fueled automobiles, most cyclic hydrocarbons are...

14

E-Print Network 3.0 - aromatic hydrocarbons progress Sample Search...  

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

Collection: Chemistry 3 Quantification of Local Ozone Production Attributable to Automobile Hydrocarbon Emissions Summary: -fueled automobiles, most cyclic hydrocarbons are...

15

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

16

Predicting tropospheric ozone and hydroxyl radical in a global, three-dimensional, chemistry, transport, and deposition model  

SciTech Connect (OSTI)

Two of the most important chemically reactive tropospheric gases are ozone (O{sub 3}) and the hydroxyl radical (OH). Although ozone in the stratosphere is a necessary protector against the sun`s radiation, tropospheric ozone is actually a pollutant which damages materials and vegetation, acts as a respiratory irritant, and is a greenhouse gas. One of the two main sources of ozone in the troposphere is photochemical production. The photochemistry is initiated when hydrocarbons and carbon monoxide (CO) react with nitrogen oxides (NO{sub x} = NO + NO{sub 2}) in the presence of sunlight. Reaction with the hydroxyl radical, OH, is the main sink for many tropospheric gases. The hydroxyl radical is highly reactive and has a lifetime on the order of seconds. Its formation is initiated by the photolysis of tropospheric ozone. Tropospheric chemistry involves a complex, non-linear set of chemical reactions between atmospheric species that vary substantially in time and space. To model these and other species on a global scale requires the use of a global, three-dimensional chemistry, transport, and deposition (CTD) model. In this work, I developed two such three dimensional CTD models. The first model incorporated the chemistry necessary to model tropospheric ozone production from the reactions of nitrogen oxides with carbon monoxide (CO) and methane (CH{sub 4}). The second also included longer-lived alkane species and the biogenic hydrocarbon isoprene, which is emitted by growing plants and trees. The models` ability to predict a number of key variables (including the concentration of O{sub 3}, OH, and other species) were evaluated. Then, several scenarios were simulated to understand the change in the chemistry of the troposphere since preindustrial times and the role of anthropogenic NO{sub x} on present day conditions.

Atherton, C.S.

1995-01-05T23:59:59.000Z

17

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

18

E-Print Network 3.0 - active natural hydrocarbon Sample Search...  

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

Biology and Medicine 2 Quantification of Local Ozone Production Attributable to Automobile Hydrocarbon Emissions Summary: Quantification of Local Ozone Production Attributable...

19

E-Print Network 3.0 - aromatic hydrocarbons affect Sample Search...  

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

Sciences and Ecology 3 Quantification of Local Ozone Production Attributable to Automobile Hydrocarbon Emissions Summary: -fueled automobiles, most cyclic hydrocarbons are...

20

E-Print Network 3.0 - aromatic hydrocarbons annual Sample Search...  

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

Page: << < 1 2 3 4 5 > >> 1 Quantification of Local Ozone Production Attributable to Automobile Hydrocarbon Emissions Summary: releases about 5 billion kilograms of hydrocarbons...

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

E-Print Network 3.0 - aromatic hydrocarbons implications Sample...  

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

Page: << < 1 2 3 4 5 > >> 1 Quantification of Local Ozone Production Attributable to Automobile Hydrocarbon Emissions Summary: -fueled automobiles, most cyclic hydrocarbons are...

22

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

23

A Micro-Computer-Based Fuel Optimization System Utilizing In-Situ Measurement of Carbon Monoxide  

E-Print Network [OSTI]

gas analyzer that mounts directly in the flue or stack to continuously measure carbon monoxide, unburned hydrocarbons, opacity and temperature. The control console interfaces directly with the boiler's existing analog control system to provide precise...

DeVivo, D. G.

1980-01-01T23:59:59.000Z

24

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

25

E-Print Network 3.0 - aromatic hydrocarbon exhaust Sample Search...  

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

Page: << < 1 2 3 4 5 > >> 1 Quantification of Local Ozone Production Attributable to Automobile Hydrocarbon Emissions Summary: : Acetylenes: Aromatics: 57 15 2 26 A breakdown of 17...

26

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

27

Investigation of the Atmospheric Ozone Impacts of Methyl Iodide  

E-Print Network [OSTI]

J. R. Holmes (1977): “Nitrogen Dioxide Photolysis in the LosO3 Ozone NO Nitric Oxide NO2 Nitrogen Dioxide NO3 NitrateNitrogen Pentoxide HONO Nitrous Acid HNO3 Nitric Acid HNO4 Peroxynitric Acid HO2H Hydrogen Peroxide CO Carbon Monoxide SO2 Sulfur Dioxide

Carter, W P L

2007-01-01T23:59:59.000Z

28

Transient PrOx carbon monoxide measurement, control, and optimization  

SciTech Connect (OSTI)

Fuel processing systems for low temperature polymer electrolyte membrane (PEM) fuel cell systems require control of the carbon monoxide concentration to less than 100 ppm to 10 ppm in the anode feed. Conventional hydrocarbon fuel processors use a water-gas shift (WGS) reactor to react CO with water to form H2 and reduce the CO concentration. The CO conversion is limited by equilibrium at the outlet temperature of the WGS reactor. The WGS outlet CO concentration can range from over 1% to 2000 ppm depending on the system and its operating parameters. At these concentrations, CO poisons low temperature PEM fuel cells and the concentrations needs to be reduced further.

Inbody, M. A. (Michael A.); Borup, R. L. (Rodney L.); Tafoya, J. (Jose I.)

2002-01-01T23:59:59.000Z

29

(Carbon monoxide metabolism by photosynthetic bacteria)  

SciTech Connect (OSTI)

Research continued on the metabolism of carbon monoxide by Rhodospirillum rubrum. This report discusses progress on the activity, induction, inhibition, and spectroscopic analysis of the enzyme Carbon Monoxide Dehydrogenase. (CBS)

Not Available

1989-01-01T23:59:59.000Z

30

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

31

Advanced Diesel Combustion with Low Hydrocarbon and Carbon Monoxide  

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

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home Page on Delicious Rank EERE:YearRound-Up fromDepartment of EnergyAdministrative RecordsBiofuelseffort toACESTIFofEmissions

32

Ozone chemistry in the smoke from the Kuwait oil fires  

SciTech Connect (OSTI)

Ozone depletion occurred in the core of the plume of smoke from the Kuwait oil fires within 100 km of the fires, primarily in regions where NO{sub x} concentrations were high and ultraviolet flux was near zero. Rapid conversion of NO to NO{sub 2} can explain almost all of the ozone loss. Ozone was produced in diffuse regions of the plume, where the ultraviolet flux was higher than in the core. However, due to the relatively high ratio of nonmethane hydrocarbons to NO{sub x}, ozone production was slow. Since ozone was produced in a much larger volume than it was depleted, the plume as a whole was a source of ozone on a regional scale. 27 refs., 4 figs., 1 tab.

Herring, J.A.; Hobbs, P.V. [Univ. of Washington, Seattle, WA (United States)

1992-09-20T23:59:59.000Z

33

Reductions in ozone concentrations due to controls on variability in industrial flare emissions in Houston, Texas  

E-Print Network [OSTI]

High concentrations of ozone in the Houston/Galveston area are associated with industrial plumes of highly reactive hydrocarbons, mixed with NOx. The emissions leading to these plumes can have significant temporal variability, ...

Nam, Junsang

2007-01-01T23:59:59.000Z

34

The effect of variability in industrial emissions on ozone formation in Houston, Texas  

E-Print Network [OSTI]

Ambient observations have indicated that high concentrations of ozone observed in the Houston/Galveston area are associated with plumes of highly reactive hydrocarbons, mixed with NOx, from industrial facilities. Ambient ...

Webster, Mort David

2007-01-01T23:59:59.000Z

35

Supporting Information for Impact of Chlorine Emissions from Sea-Salt Aerosol on Coastal Urban Ozone  

E-Print Network [OSTI]

DIOXIDE H2O2 HYDROGEN PEROXIDE NH3 AMMONIA NIT AEROSOL NITRATE SO2 SULFUR DIOXIDE SO3 SULFUR TRIOXIDE OSD extensions* NO NITRIC OXIDE NO2 NITROGEN DIOXIDE O3 OZONE HONO NITROUS ACID HNO3 NITRIC ACID HNO4 PERNITRIC ACID N2O5 NITROGEN PENTOXIDE NO3 NITRATE RADICAL HO2 HYDROPEROXY RADICAL CO CARBON MONOXIDE CO2 CARBON

Dabdub, Donald

36

Apparatus for hydrocarbon extraction  

DOE Patents [OSTI]

Systems and methods for hydrocarbon extraction from hydrocarbon-containing material. Such systems and methods relate to extracting hydrocarbon from hydrocarbon-containing material employing a non-aqueous extractant. Additionally, such systems and methods relate to recovering and reusing non-aqueous extractant employed for extracting hydrocarbon from hydrocarbon-containing material.

Bohnert, George W.; Verhulst, Galen G.

2013-03-19T23:59:59.000Z

37

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

38

Carbon Monoxide Poisoning Avoided Through Weatherization | Department...  

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

systems in recipients' homes. "We had a chain -- one right after another," says Debbie Biggs, weatherization director for C-SCDC. "One had carbon monoxide levels so high we told...

39

Atmospheric deposition of polycyclic aromatic hydrocarbons in an urban and a suburban area of Korea from 2002 to 2004  

SciTech Connect (OSTI)

Atmospheric bulk samples (wet and dry) were collected monthly during 2002 to 2004 from an urban and a suburban area in Korea for assessment of depositional flux and seasonal variations in the concentrations of polycyclic aromatic hydrocarbons (PAHs). PAH depositional flux ranged from 64.1 to 610 {mu} g/m{sup 2}/y for the urban area and from 65 to 460 {mu} g/m{sup 2}/y for the suburban area. The fluxes of PAHs measured in this study were comparable with those reported for urban and suburban areas in other countries. The fluxes of particulates and PAHs were higher in winter than in summer, consistent with the greater per capita consumption of fossil fuel in winter than in summer. Ambient temperature played a major role in the seasonal variability in PAH fluxes. Photochemical degradation of PAHs appears to occur during the summer months. The relationship of PAH depositional fluxes with major air pollutants, such as ozone, sulfur dioxide, carbon monoxide, nitrogen dioxide, and presence of particulate matter up to 10 {mu} m in size (PM10), was also investigated. Dominant PAH compounds in both the urban and the suburban locations were benzo(g,h,i)perylene, pyrene, and indeno(1,2,3-c,d)pyrene. Based on the PAH diagnostic ratios and a factor analysis, the major sources of PAHs in the urban and the suburban regions were found to be similar. Diesel exhaust, coal combustion, and gasoline emissions contributed predominantly to atmospheric PAH contamination.

Moon, H.B.; Kannan, K.; Lee, S.J.; Ok, G. [National Fisheries Research & Development Institute, Pusan (Republic of Korea)

2006-11-15T23:59:59.000Z

40

Process of producing liquid hydrocarbon fuels from biomass  

DOE Patents [OSTI]

A continuous thermochemical indirect liquefaction process is described to convert various biomass materials into diesel-type transportation fuels which fuels are compatible with current engine designs and distribution systems comprising feeding said biomass into a circulating solid fluidized bed gasification system to produce a synthesis gas containing olefins, hydrogen and carbon monoxide and thereafter introducing the synthesis gas into a catalytic liquefaction system to convert the synthesis gas into liquid hydrocarbon fuel consisting essentially of C[sub 7]-C[sub 17] paraffinic hydrocarbons having cetane indices of 50+. 1 fig.

Kuester, J.L.

1987-07-07T23:59:59.000Z

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

Process of producing liquid hydrocarbon fuels from biomass  

DOE Patents [OSTI]

A continuous thermochemical indirect liquefaction process to convert various biomass materials into diesel-type transportation fuels which fuels are compatible with current engine designs and distribution systems comprising feeding said biomass into a circulating solid fluidized bed gasification system to produce a synthesis gas containing olefins, hydrogen and carbon monoxide and thereafter introducing the synthesis gas into a catalytic liquefaction system to convert the synthesis gas into liquid hydrocarbon fuel consisting essentially of C.sub.7 -C.sub.17 paraffinic hydrocarbons having cetane indices of 50+.

Kuester, James L. (Scottsdale, AZ)

1987-07-07T23:59:59.000Z

42

Naphthenic hydrocarbons  

SciTech Connect (OSTI)

An important type of naphthenic hydrocarbons is the monocyclic type, (k/sub 2/, 0, 0). In this instance the number of carbon atoms, n = k/sub 2/, and a formula, C/sub n/H/sub 2n/, can be written where H/C = 2. The value n can vary from 2 to infinity. In the case of n = 2, it is ethylene (I) (2-membered cyclic ring); n = 3, cyclopropane (II) (3-membered cyclic ring); n = 4, cyclobutane (III) (4-membered cyclic ring); etc. If the monocyclic naphthenic is planar, then the bond angle theta can be expressed as theta = (1 - 2/n)..pi.. where n is the number of carbon atoms. However, the tetrahedron angle of the carbon atom being phi = cos/sup -1/ (- 1/3).

Yen, T.F.; Kuo, J.F.; Chilingarian, G.V.

1987-01-01T23:59:59.000Z

43

[Carbon monoxide metabolism by photosynthetic bacteria]. Progress report  

SciTech Connect (OSTI)

Research continued on the metabolism of carbon monoxide by Rhodospirillum rubrum. This report discusses progress on the activity, induction, inhibition, and spectroscopic analysis of the enzyme Carbon Monoxide Dehydrogenase. (CBS)

Not Available

1989-12-31T23:59:59.000Z

44

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

E-Print Network [OSTI]

Monoxide in Seatde Ice Skating Rinks." American Journal ofHockey Players in Ice Skating Rinks." Veterinary and Human

Apte, Michael G.

2010-01-01T23:59:59.000Z

45

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

46

Systems including catalysts in porous zeolite materials within a reactor for use in synthesizing hydrocarbons  

DOE Patents [OSTI]

Catalytic structures include a catalytic material disposed within a zeolite material. The catalytic material may be capable of catalyzing a formation of methanol from carbon monoxide and/or carbon dioxide, and the zeolite material may be capable of catalyzing a formation of hydrocarbon molecules from methanol. The catalytic material may include copper and zinc oxide. The zeolite material may include a first plurality of pores substantially defined by a crystal structure of the zeolite material and a second plurality of pores dispersed throughout the zeolite material. Systems for synthesizing hydrocarbon molecules also include catalytic structures. Methods for synthesizing hydrocarbon molecules include contacting hydrogen and at least one of carbon monoxide and carbon dioxide with such catalytic structures. Catalytic structures are fabricated by forming a zeolite material at least partially around a template structure, removing the template structure, and introducing a catalytic material into the zeolite material.

Rolllins, Harry W. (Idaho Falls, ID); Petkovic, Lucia M. (Idaho Falls, ID); Ginosar, Daniel M. (Idaho Falls, ID)

2012-07-24T23:59:59.000Z

47

Methods of using structures including catalytic materials disposed within porous zeolite materials to synthesize hydrocarbons  

DOE Patents [OSTI]

Catalytic structures include a catalytic material disposed within a zeolite material. The catalytic material may be capable of catalyzing a formation of methanol from carbon monoxide and/or carbon dioxide, and the zeolite material may be capable of catalyzing a formation of hydrocarbon molecules from methanol. The catalytic material may include copper and zinc oxide. The zeolite material may include a first plurality of pores substantially defined by a crystal structure of the zeolite material and a second plurality of pores dispersed throughout the zeolite material. Systems for synthesizing hydrocarbon molecules also include catalytic structures. Methods for synthesizing hydrocarbon molecules include contacting hydrogen and at least one of carbon monoxide and carbon dioxide with such catalytic structures. Catalytic structures are fabricated by forming a zeolite material at least partially around a template structure, removing the template structure, and introducing a catalytic material into the zeolite material.

Rollins, Harry W. (Idaho Falls, ID); Petkovic, Lucia M. (Idaho Falls, ID); Ginosar, Daniel M. (Idaho Falls, ID)

2011-02-01T23:59:59.000Z

48

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

49

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

50

Catalysts and process for liquid hydrocarbon fuel production  

DOE Patents [OSTI]

The present invention provides a novel process and system in which a mixture of carbon monoxide and hydrogen synthesis gas, or syngas, is converted into hydrocarbon mixtures composed of high quality gasoline components, aromatic compounds, and lower molecular weight gaseous olefins in one reactor or step. The invention utilizes a novel molybdenum-zeolite catalyst in high pressure hydrogen for conversion, as well as a novel rhenium-zeolite catalyst in place of the molybdenum-zeolite catalyst, and provides for use of the novel catalysts in the process and system of the invention.

White, Mark G; Liu, Shetian

2014-12-09T23:59:59.000Z

51

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... .)...

52

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

53

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

54

7, 97959828, 2007 Tropospheric ozone  

E-Print Network [OSTI]

ACPD 7, 9795­9828, 2007 Tropospheric ozone climatology over Beijing A. J. Ding et al. Title Page Chemistry and Physics Discussions Tropospheric ozone climatology over Beijing: analysis of aircraft data;ACPD 7, 9795­9828, 2007 Tropospheric ozone climatology over Beijing A. J. Ding et al. Title Page

Paris-Sud XI, Université de

55

8, 1106311101, 2008 Tropospheric Ozone  

E-Print Network [OSTI]

ACPD 8, 11063­11101, 2008 Tropospheric Ozone climatology in the southern subtropics G. Clain et al.0 License. Atmospheric Chemistry and Physics Discussions Tropospheric ozone climatology at two southern Tropospheric Ozone climatology in the southern subtropics G. Clain et al. Title Page Abstract Introduction

Paris-Sud XI, Université de

56

Carbon monoxide sensor for PEM fuel cell systems Christopher T. Holta,*  

E-Print Network [OSTI]

reforming) or with air and water (autothermal reforming). In the second step, carbon monoxide is reduced

Azad, Abdul-Majeed

57

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

58

Ozone decomposing filter  

DOE Patents [OSTI]

In an improved ozone decomposing air filter carbon fibers are held together with a carbonized binder in a perforated structure. The structure is made by combining rayon fibers with gelatin, forming the mixture in a mold, freeze-drying, and vacuum baking.

Simandl, Ronald F. (Farragut, TN); Brown, John D. (Harriman, TN); Whinnery, Jr., LeRoy L. (Dublin, CA)

1999-01-01T23:59:59.000Z

59

The oxidation of soot and carbon monoxide in hydrocarbon diffusion flames  

SciTech Connect (OSTI)

Quantitative hydroxyl radical concentrations and primary soot particle sizes have been determined in the soot oxidation regions of axisymmetric diffusion flames burning methane, methane/butane, and methane/1-butene in air at atmospheric pressure. The total carbon flow rate was held constant in these flames while the maximum amount of soot varied by a factor of seven along the centerline. Laser-induced fluorescence measurements of OH were placed on an absolute basis by calibration against earlier absorption results. The primary size measurements of the soot particles were made using thermophoretic sampling and transmission electron microscopy. OH concentrations are greatly reduced in the presence of soot particles. Whereas large super-equilibrium ratios are observed in the high-temperature reaction zones in the absence of soot, the OH concentrations approach equilibrium values when the soot loading is high. The diminished OH concentrations are found to arise from reactions with the soot particles and only to a minor degree from lower temperatures due to soot radiation losses. Analysis of the soot oxidation rates computed from the primary particle size profiles as a function of time along the flame centerlines shows that OH is the dominant oxidizer of soot, with O[sub 2] making only a small contribution. Higher collision efficiencies of OH reactions with soot particles are found for the flames containing larger soot concentrations at lower temperatures. A comparison of the soot and CO oxidation rates shows that although CO is inherently more reactive than soot, the soot successfully competes with CO for OH and hence suppresses CO oxidation for large soot concentrations.

Puri, R.; Santoro, R.J. (Pennsylvania State Univ., University Park, PA (United States). Dept. of Mechanical Engineering); Smyth, K.C. (National Inst. of Standards and Technology, Gaithersburg, MD (United States). Building and Fire Research Lab.)

1994-05-01T23:59:59.000Z

60

NATURAL MARINE HYDROCARBON SEEPAGE  

E-Print Network [OSTI]

affects ocean chemistry (Dando and Hovland, 1992) and provides a natural source of petroleum pollution the water column above submarine vents, plumes of hydrocarbon gas bubbles act as acoustic scattering targets

Luyendyk, Bruce

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

Hydrocarbon desulfurization process  

SciTech Connect (OSTI)

A process is described for converting a sour hydrocarbon feedstock having a relatively high sulfur content to a hydrocarbon product having a relatively low sulfur content comprising the steps of: (a) hydrodesulfurizing the feedstock having a relatively high sulfur contact with hydrogen to produce the hydrocarbon product having a relatively low sulfur content and hydrogen sulfide gas; (b) contacting the hydrogen sulfide gas with an anthraquinone dissolved in a polar organic solvent having a polarity greater than about 3 Debye units to produce sulfur and an anthrahydroquinone in the solvent; (c) regenerating the anthraquinone from the anthrahydroquinone upon contact with air to produce the anthraquinone and hydrogen peroxide; (d) recycling the anthraquinone to step (b); (e) reducing the hydrogen peroxide to oxygen and water; (f) partially oxidizing a hydrocarbon fuel with the oxygen to produce carbon dioxide and hydrogen; and (g) recycling the hydrogen to step (a).

Plummer, M.A.; Zimmerman, C.C. Jr.

1986-04-08T23:59:59.000Z

62

Membrane separation of hydrocarbons  

DOE Patents [OSTI]

Mixtures of heavy oils and light hydrocarbons may be separated by passing the mixture over a polymeric membrane which comprises a polymer capable of maintaining its integrity in the presence of hydrocarbon compounds at temperature ranging from about ambient to about 100.degree. C. and pressures ranging from about 50 to about 1000 psi. The membranes which possess pore sizes ranging from about 10 to about 500 Angstroms are cast from a solvent solution and recovered.

Funk, Edward W. (Highland Park, IL); Kulkarni, Sudhir S. (Hoffman Estates, IL); Chang, Y. Alice (Des Plaines, IL)

1986-01-01T23:59:59.000Z

63

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

64

Dispersant solutions for dispersing hydrocarbons  

DOE Patents [OSTI]

A dispersant solution includes a hydrocarbon dispersing solution derived from a bacterium from ATCC 75527, ATCC 75529, or ATCC 55638.

Tyndall, Richard L. (Clinton, TN)

1997-01-01T23:59:59.000Z

65

Dispersant solutions for dispersing hydrocarbons  

DOE Patents [OSTI]

A dispersant solution includes a hydrocarbon dispersing solution derived from a bacterium from ATCC 75527, ATCC 75529, or ATCC 55638.

Tyndall, R.L.

1997-03-11T23:59:59.000Z

66

Hydrocarbon cracking catalyst  

SciTech Connect (OSTI)

This patent describes a catalyst composition for cracking hydrocarbons to maximize gasoline comprising: rare earth exchanged ''Y'' crystalline faujasite dispersed in a clay containing matrix material; and which has been subsequently further ion exchanged to contain 0.20 to 3.0 wt% yttrium, calculated as the oxide, whereby the yttrium is chemically combined in the catalyst composition.

Lochow, C.F.; Kovacs, D.B.

1988-12-27T23:59:59.000Z

67

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

68

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.

69

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.

70

Ambient aromatic hydrocarbon measurements at Welgegund, South Africa  

SciTech Connect (OSTI)

Aromatic hydrocarbons are associated with direct adverse human health effects and can have negative impacts on ecosystems due to their toxicity, as well as indirect negative effects through the formation of tropospheric ozone and secondary organic aerosol that affect human health, crop production and regional climate. Measurements were conducted at the Welgegund measurement station (South Africa) that is considered to be a regionally representative background site. However, the site is occasionally impacted by plumes from major anthropogenic source regions in the interior of South Africa, which include the western Bushveld Igneous Complex (e.g. platinum, base metal and ferrochrome smelters), the eastern Bushveld Igneous Complex (platinum and ferrochrome smelters), the Johannesburg-Pretoria metropolitan conurbation (>10 million people), the Vaal Triangle (e.g. petrochemical and industries), the Mpumalanga Highveld (e.g. coal-fired power plants and petrochemical industry) and also a region of anti-cyclonic recirculation of air mass over the interior of South Africa. The aromatic hydrocarbon measurements were conducted with an automated sampler on Tenax-TA and Carbopack-B adsorbent tubes with heated inlet for one year. Samples were collected twice a week for two hours during daytime and two hours 1 during night-time. A thermal desorption unit, connected to a gas chromatograph and a mass 2 selective detector was used for sample preparation and analysis. Results indicated that the 3 monthly median total aromatic hydrocarbon concentrations ranged between 0.01 to 3.1 ppb. 4 Benzene levels did not exceed local air quality standards. Toluene was the most abundant 5 species, with an annual median concentration of 0.63 ppb. No statistically significant 6 differences in the concentrations measured during daytime and night-time were found and no distinct seasonal patterns were observed. Air mass back trajectory analysis proved that the lack of seasonal cycles could be attributed to patterns determining the origin of the air masses sampled. Aromatic hydrocarbon concentrations were in general significantly higher in air masses that passed over anthropocentrically impacted regions. Interspecies correlations and ratios gave some indications of the possible sources for the different aromatic hydrocarbons in the source regions defined in the paper. The highest contribution of aromatic hydrocarbon concentrations to ozone formation potential was also observed in plumes passing over anthropocentrically impacted regions.

Jaars, K.; Beukes, J. P.; van Zyl, P. G.; Venter, A. D.; Josipovic, M.; Pienaar, J. J.; Vakkari, Ville; Aaltonen, H.; Laakso, H.; Kulmala, M.; Tiitta, P.; Guenther, Alex B.; Hellen, H.; Laakso, L.; Hakola, H.

2014-07-11T23:59:59.000Z

71

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.

72

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

73

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

74

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

75

Quantitative analysis of SCIAMACHY carbon monoxide total column measurements  

E-Print Network [OSTI]

, SCIAMACHY CO total column retrievals are of sufficient quality to provide useful new information]. Ground-based FTIR measurements provide high quality total column measurements but have very limitedQuantitative analysis of SCIAMACHY carbon monoxide total column measurements A. T. J. de Laat,1,2 A

Laat, Jos de

76

Membrane separation of hydrocarbons  

DOE Patents [OSTI]

Mixtures of heavy oils and light hydrocarbons may be separated by passing the mixture through a polymeric membrane. The membrane which is utilized to effect the separation comprises a polymer which is capable of maintaining its integrity in the presence of hydrocarbon compounds and which has been modified by being subjected to the action of a sulfonating agent. Sulfonating agents which may be employed will include fuming sulfuric acid, chlorosulfonic acid, sulfur trioxide, etc., the surface or bulk modified polymer will contain a degree of sulfonation ranging from about 15 to about 50%. The separation process is effected at temperatures ranging from about ambient to about 100.degree. C. and pressures ranging from about 50 to about 1000 psig.

Chang, Y. Alice (Des Plaines, IL); Kulkarni, Sudhir S. (Hoffman Estates, IL); Funk, Edward W. (Highland Park, IL)

1986-01-01T23:59:59.000Z

77

Direct hydrocarbon fuel cells  

DOE Patents [OSTI]

The direct electrochemical oxidation of hydrocarbons in solid oxide fuel cells, to generate greater power densities at lower temperatures without carbon deposition. The performance obtained is comparable to that of fuel cells used for hydrogen, and is achieved by using novel anode composites at low operating temperatures. Such solid oxide fuel cells, regardless of fuel source or operation, can be configured advantageously using the structural geometries of this invention.

Barnett, Scott A.; Lai, Tammy; Liu, Jiang

2010-05-04T23:59:59.000Z

78

Water addition for increased CO/H[sub 2] hydrocarbon synthesis activity over catalysts comprising cobalt, ruthenium and mixtures thereof which may include a promoter metal  

SciTech Connect (OSTI)

A once-through, fixed or slurry bed Fischer Tropsch process is described with enhanced CO conversion activity and C[sub 5] + liquid hydrocarbon selectivity comprising contacting a feed mixture of carbon monoxide and hydrogen in a reaction zone with about 1 Vol % to about 70 Vol % water based on the total volume of feed mixture, at a pressure above one atmosphere and a temperature ranging from about 150 C to about 300 C, with a catalyst selected from the group consisting of cobalt, ruthenium, and mixtures thereof on a titania support, wherein said titania support is less than 40 m[sup 2]/g, converting at least 90 Vol % of the carbon monoxide to liquid hydrocarbons, and in the substantial absence of CO[sub 2] formation.

Kim, C.J.

1993-07-13T23:59:59.000Z

79

Process for separating an ethylenically unsaturated hydrocarbon from a hydrocarbon mixture  

SciTech Connect (OSTI)

A process is described for separating an ethylenically unsaturated hydrocarbon from a hydrocarbon mixture characterized by: (a) distilling a hydrocarbon mixture containing the unsaturated hydrocarbon with an N-(aminoalkyl) piperazine; and (b) separating the amine/hydrocarbon mixture into at least two factions, one of which contains the amine and the unsaturated hydrocarbon.

vanEijl, A.T.

1986-06-24T23:59:59.000Z

80

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

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

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

82

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

83

Hydrocarbon conversion catalysts  

SciTech Connect (OSTI)

This patent describes a process for hydrocracking hydrocarbon oils into products of lower average molecular weight and lower average boiling point. It comprises contacting a hydrocarbon oil at a temperature between 250{sup 0}C and 500{sup 0}C and a pressure up to 300 bar in the presence of hydrogen with a catalyst consisting essentially of a Y zeolite modified to have a unit cell size below 24.35A, a water absorption capacity (at 25{sup 0}C and a rho/rho/sub o/ value of 0.2) of at least 8% by weight of the zeolite and a pore volume of at least 0.25 ml/g wherein between 10% and 60% of the total pore volume is made up of pores having a diameter of at least 8 nm; an alumina binder and at least one hydrogenation component selected from the group consisting of a Group VI metal, a Group VIII metal and mixtures thereof.

Hoek, A.; Huizinga, T.; Maxwell, I.E.

1989-08-15T23:59:59.000Z

84

E-Print Network 3.0 - air pollutants ozone Sample Search Results  

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

1 Global Ozone Project Ozone Formation in Summary: , power plants and industry all emit air pollution that forms ground-level ozone. Ozone is a primary... Stratospheric and...

85

Hydrocarbon sensors and materials therefor  

DOE Patents [OSTI]

An electrochemical hydrocarbon sensor and materials for use in sensors. A suitable proton conducting electrolyte and catalytic materials have been found for specific application in the detection and measurement of non-methane hydrocarbons. The sensor comprises a proton conducting electrolyte sandwiched between two electrodes. At least one of the electrodes is covered with a hydrocarbon decomposition catalyst. Two different modes of operation for the hydrocarbon sensors can be used: equilibrium versus non-equilibrium measurements and differential catalytic. The sensor has particular application for on-board monitoring of automobile exhaust gases to evaluate the performance of catalytic converters. In addition, the sensor can be utilized in monitoring any process where hydrocarbons are exhausted, for instance, industrial power plants. The sensor is low cost, rugged, sensitive, simple to fabricate, miniature, and does not suffer cross sensitivities.

Pham, Ai Quoc (San Jose, CA); Glass, Robert S. (Livermore, CA)

2000-01-01T23:59:59.000Z

86

Process for recovering hydrocarbons from a hydrocarbon-bearing formation  

SciTech Connect (OSTI)

A method is described for transporting heavy crude oil through a pipeline which involves introducing into a pipeline or well-bore with the viscous hydrocarbons an aqueous solution containing (1) a sulfonate surfactant, (2) a rosin soap or a naphthenic acid soap and, optionally (3) coupling agent whereby there is spontaneously formed a low viscosity, salt tolerant, oil-in-water emulsion. Also disclosed is a method of recovery of hydrocarbons from a hydrocarbon bearing formation employing an aqueous solution containing (1) a sulfonate surfactant, (2) a rosin soap or a naphthenic acid soap and, optionally (3) a coupling agent.

Alston, R.B.; Braden, W.B.; Flournoy, K.H.

1980-03-11T23:59:59.000Z

87

TEXIN2: a model for predicting carbon monoxide concentrations near intersections  

E-Print Network [OSTI]

reduction caused by congestion 49 10 Application of impedance factors Carbon monoxide emissions for vehicular speed changes 59 12 Pasquill stability classes, A-G, as related to wind speed and incoming solar radiation 77 13 Regression lines... The prediction of carbon monoxide concentrations near roadway intersections represents a serious and challenging problem in air pollution research. In many geographical regions, the major portion of carbon monoxide in the environment is attributable...

Korpics, J. J

1985-01-01T23:59:59.000Z

88

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

89

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

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

reservoirs (storages, especially the atmosphere, terrestrial biosphere, oceans... emissions trading and the control of greenhouse gas emissions. Carbon monoxide a chemical...

90

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...

91

Ozone Reductions Using Residential Building Envelopes  

SciTech Connect (OSTI)

Ozone is an air pollutant with that can have significant health effects and a significant source of ozone in some regions of California is outdoor air. Because people spend the vast majority of their time indoors, reduction in indoor levels of ozone could lead to improved health for many California residents. Ozone is removed from indoor air by surface reactions and can also be filtered by building envelopes. The magnitude of the envelope impact depends on the specific building materials that the air flows over and the geometry of the air flow paths through the envelope that can be changes by mechanical ventilation operation. The 2008 Residential Building Standards in California include minimum requirements for mechanical ventilation by referencing ASHRAE Standard 62.2. This study examines the changes in indoor ozone depending on the mechanical ventilation system selected to meet these requirements. This study used detailed simulations of ventilation in a house to examine the impacts of different ventilation systems on indoor ozone concentrations. The simulation results showed that staying indoors reduces exposure to ozone by 80percent to 90percent, that exhaust ventilation systems lead to lower indoor ozone concentrations, that opening of windows should be avoided at times of high outdoor ozone, and that changing the time at which mechanical ventilation occurs has the ability to halve exposure to ozone. Future work should focus on the products of ozone reactions in the building envelope and the fate of these products with respect to indoor exposures.

Walker, Iain S.; Sherman, Max; Nazaroff, William W.

2009-02-01T23:59:59.000Z

92

Ozone decomposition in water solutions  

E-Print Network [OSTI]

. Hewes, III; B. S. , Texas ASH University Directed by Dr. R. R. Davison The rate of the decomposition of ozone in water solutions at various pH's and temperatures were ob- tained by an iodometrical method. The orders of the reactions and the reaction...

Hewes, Cecil Grayson

1969-01-01T23:59:59.000Z

93

6, 74277469, 2006 Linear ozone  

E-Print Network [OSTI]

from biases in the schemes' climatology coefficients. Cariolle v2.1 analyses showed biases of up to 20 and Kelder (1998) ozone climatology into the scheme. Chem2D-OPP v2.1 analyses showed biases up to 20 analysed temperatures and the temperature climatology supplied with the scheme. Future developments should

Boyer, Edmond

94

2, 15091543, 2002 Ozone production  

E-Print Network [OSTI]

.atmos-chem-phys.org/acpd/2/1509/ c European Geosciences Union 2002 Atmospheric Chemistry and Physics Discussions Ozone as a consequence of local catabatic winds. Aver- age mid-day peroxy radical concentrations at Mt. Cimone; Atlas and Ridley, 1996; Fischer et al., 1998; Zanis et al., 2000a, b). Often, free tropospheric

Boyer, Edmond

95

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

96

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

97

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. Keywords: Carbon monoxide; Hydrogen; Syngas; Ignition; Rapid compression facility 1. Introduction Syngas

Wooldridge, Margaret S.

98

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

99

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

DOE Patents [OSTI]

The present invention relates to a method of removing of nitrogen monoxide from a nitrogen monoxide-containing gas which method comprises contacting a nitrogen oxide-containing gas with an aqueous solution of water soluble organic compound-iron ion chelate complex. The NO absorption efficiency of ferrous urea-dithiocarbamate and ferrous diethanolamine-xanthate as a function of time, oxygen content and solution ph is presented. 3 figs., 1 tab.

Liu, D. Kwok-Keung; Chang, Shih-Ger

1987-08-25T23:59:59.000Z

100

Ozone production in transpacific Asian pollution plumes and implications for ozone air quality in California  

E-Print Network [OSTI]

Ozone production in transpacific Asian pollution plumes and implications for ozone air quality in transpacific Asian pollution plumes, and the implications for ozone air quality in California, by using pollution plumes. Strong dilution of Asian pollution plumes takes place during entrainment in the U

Park, Rokjin

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

Discharge cell for ozone generator  

DOE Patents [OSTI]

A discharge cell for use in an ozone generator is provided which can suppress a time-related reduction in ozone concentration without adding a catalytic gas such as nitrogen gas to oxygen gas as a raw material gas. The discharge cell includes a pair of electrodes disposed in an opposed spaced relation with a discharge space therebetween, and a dielectric layer of a three-layer structure consisting of three ceramic dielectric layers successively stacked on at least one of the electrodes, wherein a first dielectric layer of the dielectric layer contacting the one electrode contains no titanium dioxide, wherein a second dielectric layer of the dielectric layer exposed to the discharge space contains titanium dioxide in a metal element ratio of not lower than 10 wt %.

Nakatsuka, Suguru (Amagasaki, JP)

2000-01-01T23:59:59.000Z

102

Y-12 Plant Stratospheric Ozone Protection plan  

SciTech Connect (OSTI)

The Y-12 Plant staff is required by Lockheed Martin Energy Systems (Energy Systems) (formerly Martin Marietta Energy Systems) standard ESS-EP-129 to develop and implement a Stratospheric Ozone Protection Program which will minimize emissions of ozone-depleting substances to the environment and maximize the use of ozone-safe alternatives in order to comply with Title VI of the 1990 Clean Air Act (CAA) Amendments and the implementing regulations promulgated by the Environmental Protection Agency (EPA). This plan describes the requirements, initiatives, and accomplishments of the Y-12 Plant Stratospheric Ozone Protection Program.

NONE

1995-09-01T23:59:59.000Z

103

Tropospheric Ozone Pollution and Personal Exposure  

E-Print Network [OSTI]

://www.nctcog.org/trans/air/ozone/formation.gif #12;Health Effects · Chest pain, coughing, throat irritation, and congestion · Wheezing and difficulty

Toohey, Darin W.

104

Ozone production rate and hydrocarbon reactivity in 5 urban areas: A cause of high ozone concentration in Houston  

E-Print Network [OSTI]

petrochemical complexes in the world. As a consequence the concentration of O3 in the Houston metropolitan area are ubiquitous in urban areas, the major source categories being on and off-road vehicles, power plants from nearby petrochemical facili- ties. A comparison between Houston and 4 other cities (Nashville, TN

105

DOE's Studies of Weekday/Weekend Ozone Pollution in Southern...  

Energy Savers [EERE]

DOE's Studies of WeekdayWeekend Ozone Pollution in Southern California DOE's Studies of WeekdayWeekend Ozone Pollution in Southern California 2002 DEER Conference Presentation:...

106

Weekday and Weekend Air Pollutant Levels in Ozone Problem Areas...  

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

Ambient Ozone Formation as a Function of NOx Reductions Summary and Implications for Air Quality Impacts DOE's Studies of WeekdayWeekend Ozone Pollution in Southern...

107

The Weekend Ozone Effect - The Weekly Ambient Emissions Control...  

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

More Documents & Publications WeekendWeekday Ozone Study in the South Coast Air Basin DOE's Studies of WeekdayWeekend Ozone Pollution in Southern California...

108

Correlation between speciated hydrocarbon emissions and flame ionization detector response for gasoline/alcohol blends .  

SciTech Connect (OSTI)

The U.S. renewable fuel standard has made it a requirement to increase the production of ethanol and advanced biofuels to 36 billion by 2022. Ethanol will be capped at 15 billion, which leaves 21 billion to come from other sources such as butanol. Butanol has a higher energy density and lower affinity for water than ethanol. Moreover, alcohol fueled engines in general have been shown to positively affect engine-out emissions of oxides of nitrogen and carbon monoxide compared with their gasoline fueled counterparts. In light of these developments, the variety and blend levels of oxygenated constituents is likely to increase in the foreseeable future. The effect on engine-out emissions for total hydrocarbons is less clear due to the relative insensitivity of the flame ionization detector (FID) toward alcohols and aldehydes. It is well documented that hydrocarbon (HC) measurement using a conventional FID in the presence of oxygenates in the engine exhaust stream can lead to a misinterpretation of HC emissions trends for alcohol fuel blends. Characterization of the exhaust stream for all expected hydrocarbon constituents is required to accurately determine the actual concentration of unburned fuel components in the exhaust. In addition to a conventional exhaust emissions bench, this characterization requires supplementary instrumentation capable of hydrocarbon speciation and response factor independent quantification. Although required for certification testing, this sort of instrumentation is not yet widely available in engine development facilities. Therefore, an attempt is made to empirically determine FID correction factors for oxygenate fuels. Exhaust emissions of an engine fueled with several blends of gasoline and ethanol, n-butanol and iso-Butanol were characterized using both a conventional FID and a Fourier transform infrared. Based on these results, a response factor predicting the actual hydrocarbon emissions based solely on FID results as a function of alcohol type and content is presented. Finally, the correlation derived from data presented in this study is compared with equations and results found in the literature.

Wallner, T. (Energy Systems)

2011-08-01T23:59:59.000Z

109

Enrichment of light hydrocarbon mixture  

SciTech Connect (OSTI)

Light hydrocarbon enrichment is accomplished using a vertically oriented distillation column having a plurality of vertically oriented, nonselective micro/mesoporous hollow fibers. Vapor having, for example, both propylene and propane is sent upward through the distillation column in between the hollow fibers. Vapor exits neat the top of the column and is condensed to form a liquid phase that is directed back downward through the lumen of the hollow fibers. As vapor continues to ascend and liquid continues to countercurrently descend, the liquid at the bottom of the column becomes enriched in a higher boiling point, light hydrocarbon (propane, for example) and the vapor at the top becomes enriched in a lower boiling point light hydrocarbon (propylene, for example). The hollow fiber becomes wetted with liquid during the process.

Yang; Dali (Los Alamos, NM); Devlin, David (Santa Fe, NM); Barbero, Robert S. (Santa Cruz, NM); Carrera, Martin E. (Naperville, IL); Colling, Craig W. (Warrenville, IL)

2010-08-10T23:59:59.000Z

110

Enrichment of light hydrocarbon mixture  

DOE Patents [OSTI]

Light hydrocarbon enrichment is accomplished using a vertically oriented distillation column having a plurality of vertically oriented, nonselective micro/mesoporous hollow fibers. Vapor having, for example, both propylene and propane is sent upward through the distillation column in between the hollow fibers. Vapor exits neat the top of the column and is condensed to form a liquid phase that is directed back downward through the lumen of the hollow fibers. As vapor continues to ascend and liquid continues to countercurrently descend, the liquid at the bottom of the column becomes enriched in a higher boiling point, light hydrocarbon (propane, for example) and the vapor at the top becomes enriched in a lower boiling point light hydrocarbon (propylene, for example). The hollow fiber becomes wetted with liquid during the process.

Yang, Dali (Los Alamos, NM); Devlin, David (Santa Fe, NM); Barbero, Robert S. (Santa Cruz, NM); Carrera, Martin E. (Naperville, IL); Colling, Craig W. (Warrenville, IL)

2011-11-29T23:59:59.000Z

111

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

112

Methanation of gas streams containing carbon monoxide and hydrogen  

DOE Patents [OSTI]

Carbon monoxide-containing gas streams having a relatively high concentration of hydrogen are pretreated so as to remove the hydrogen in a recoverable form for use in the second step of a cyclic, essentially two-step process for the production of methane. The thus-treated streams are then passed over a catalyst to deposit a surface layer of active surface carbon thereon essentially without the formation of inactive coke. This active carbon is reacted with said hydrogen removed from the feed gas stream to form methane. The utilization of the CO in the feed gas stream is appreciably increased, enhancing the overall process for the production of relatively pure, low-cost methane from CO-containing waste gas streams.

Frost, Albert C. (Congers, NY)

1983-01-01T23:59:59.000Z

113

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

114

Biological enhancement of hydrocarbon extraction  

DOE Patents [OSTI]

A method of microbial enhanced oil recovery for recovering oil from an oil-bearing rock formation is provided. The methodology uses a consortium of bacteria including a mixture of surfactant producing bacteria and non-surfactant enzyme producing bacteria which may release hydrocarbons from bitumen containing sands. The described bioprocess can work with existing petroleum recovery protocols. The consortium microorganisms are also useful for treatment of above oil sands, ground waste tailings, subsurface oil recovery, and similar materials to enhance remediation and/or recovery of additional hydrocarbons from the materials.

Brigmon, Robin L. (North Augusta, SC); Berry, Christopher J. (Aiken, SC)

2009-01-06T23:59:59.000Z

115

Estimating The Thermodynamics And Kinetics Of Chlorinated Hydrocarbon...  

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

Estimating The Thermodynamics And Kinetics Of Chlorinated Hydrocarbon Degradation. Estimating The Thermodynamics And Kinetics Of Chlorinated Hydrocarbon Degradation. Abstract: Many...

116

aromatic hydrocarbon components: Topics by E-print Network  

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

AROMATIC HYDROCARBONS 2005 April 19 ABSTRACT Interstellar polycyclic aromatic hydrocarbon (PAH) infrared emission features 26 Dehydrogenation of polycyclic aromatic...

117

An Assessment of Tropospheric Ozone Pollution  

E-Print Network [OSTI]

An Assessment of Tropospheric Ozone Pollution --A North American Perspective-- Surface Urban, California 94304 #12;AN ASSESSMENT OF TROPOSPHERIC OZONE POLLUTION: A NORTH AMERICAN PERSPECTIVE The NARSTO, Instituto Mexicano del Petroleo, Mexico, D.F., Mexico Alan Dunker, General Motors Research & Development

118

Syngas Upgrading to Hydrocarbon Fuels Technology Pathway  

SciTech Connect (OSTI)

This technology pathway case investigates the upgrading of woody biomass derived synthesis gas (syngas) to hydrocarbon biofuels. While this specific discussion focuses on the conversion of syngas via a methanol intermediate to hydrocarbon blendstocks, there are a number of alternative conversion routes for production of hydrocarbons through a wide array of intermediates from syngas. Future work will also consider the variations to this pathway to determine the most economically viable and lowest risk conversion route. Technical barriers and key research needs have been identified that should be pursued for the syngas-to-hydrocarbon pathway to be competitive with petroleum-derived gasoline-, diesel- and jet-range hydrocarbon blendstocks.

Talmadge, M.; Biddy, M.; Dutta, A.; Jones, S.; Meyer, A.

2013-03-01T23:59:59.000Z

119

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

120

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

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

Laboratory measurement of secondary pollutant yields from ozone reaction with HVAC filters.  

E-Print Network [OSTI]

from Ozone Reaction with HVAC Filters Hugo Destaillats,from Ozone Reaction with HVAC Filters Hugo Destaillatsfrom Ozone Reaction with HVAC Filters Hugo Destaillats

Destaillats, Hugo

2012-01-01T23:59:59.000Z

122

E-Print Network 3.0 - aura-omi tropospheric ozone Sample Search...  

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

atmospheric ozone. The Ozone Monitoring Instrument (OMI) onboard the satellite provides global total column ozone (TCO) and in combination Summary: with other instruments...

123

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

124

Dry reforming of hydrocarbon feedstocks  

SciTech Connect (OSTI)

Developments in catalyst technology for the dry reforming of hydrocarbon feedstocks are reviewed for methane, higher hydrocarbons and alcohols. Thermodynamics, mechanisms and the kinetics of dry reforming are also reviewed. The literature on Ni catalysts, bi-metallic Ni catalysts and the role of promoters on Ni catalysts is critically evaluated. The use of noble and transitional metal catalysts for dry reforming is discussed. The application of solid oxide and metal carbide catalysts to dry reforming is also evaluated. Finally, various mechanisms for catalyst deactivation are assessed. This review also examines the various process related issues associated with dry reforming such as its application and heat optimization. Novel approaches such as supercritical dry reforming and microwave assisted dry reforming are briefly expanded upon.

Shah, Yatish T. [Norfolk State University; Gardner, Todd H. [U.S. DOE

2014-01-01T23:59:59.000Z

125

Underground caverns for hydrocarbon storage  

SciTech Connect (OSTI)

Large, international gas processing projects and growing LPG imports in developing countries are driving the need to store large quantities of hydrocarbon liquids. Even though underground storage is common in the US, many people outside the domestic industry are not familiar with the technology and the benefits underground storage can offer. The latter include lower construction and operating costs than surface storage, added safety, security and greater environmental acceptance.

Barron, T.F. [Exeter Energy Services, Houston, TX (United States)

1998-12-31T23:59:59.000Z

126

Deep desulfurization of hydrocarbon fuels  

DOE Patents [OSTI]

The invention relates to processes for reducing the sulfur content in hydrocarbon fuels such as gasoline, diesel fuel and jet fuel. The invention provides a method and materials for producing ultra low sulfur content transportation fuels for motor vehicles as well as for applications such as fuel cells. The materials and method of the invention may be used at ambient or elevated temperatures and at ambient or elevated pressures without the need for hydrogen.

Song, Chunshan (State College, PA); Ma, Xiaoliang (State College, PA); Sprague, Michael J. (Calgary, CA); Subramani, Velu (State College, PA)

2012-04-17T23:59:59.000Z

127

17 October 2014 Antarctic Ozone Bulletin  

E-Print Network [OSTI]

as measured with an electrochemical ozonesonde on 10 October. One can see two large "bite-outs" of ozone). Ushuaia is marked with a green dot. One can see that Ushuaia is well inside the polar vortex. The PV data

Toohey, Darin W.

128

Ozone treatment of biomass to enhance digestibility  

E-Print Network [OSTI]

is very resistant to enzymatic degradation. Lignocellulosic materials require pretreatment to enhance their digestibility. The main objective of this research was to further enhance the digestibility of biomass (bagasse) with ozonation as a follow...

Almendarez, Maria Elena

2000-01-01T23:59:59.000Z

129

Pinatubo fails to deepen the ozone hole  

SciTech Connect (OSTI)

When the Philippine volcano Pinatubo exploded last year, pumping the upper atmosphere full of find debris, researchers foresaw yet another assault on the stratosphere's beleaguered ozone layer. Some calculations of the effects of volcanic debris implied that as much as 25% to 30% of the ozone shield over temperature latitudes might be eaten away by the volcanic haze - five times the observed loss over the past decade. Early measurements didn't bear out that concern, but researchers weren't prepared to call off the alarm until the verdict came in from the most vulnerable part of the planet's ozone layer, the frigid stratosphere over Antarctica. Although the hole was more extensive than ever before, probably because of unusual weather patterns, total ozone bottomed out well above the record set last year - even a tad above the low levels seen in 1987, 1989, and 1990.

Kerr, R.A.

1992-10-15T23:59:59.000Z

130

Methane production from ozonated pulp mill effluent  

SciTech Connect (OSTI)

A study was made of the production of methane from desugared spent sulfite liquor (SSL) reacted with ozone. The ozonated SSL was fed continuously to three anaerobic fermenters for three months as the sole source of carbon and energy. The fermenters were inoculated with anaerobic bacteria obtained from sewage sludge and acclimated for 1 month in ozonated SSL prior to continuous fermentation. Chemical and biological parameters such as COD, BOD, total sulfur content, redox potential, pH, fatty acid composition, and methane bacteria populations were monitored to determine changes in the SSL during fermentation. Methane production from ozone-treated SSL averaged 1.7 liters/ liter or 17 ml of CH/sub 4/ produced/gram of volatile solids fed. Fatty acis analysis of fermenter effluent indicated a net production of 58 mM/ liter of acetate during ozonated SSL fermentation. This acetic acid production shows future potential for further fermentation by protein-producing yeast. Although the rate of conversion of volatile solids to CH/sub 4/ in this process was not competitive with domestic or agricultural waste digesters, this study did indicate the potential benefits of ozonating organic wastes for increased methane fermentation yields.

Bremmon, C.E.; Jurgensen, M.F.; Patton, J.T.

1980-07-01T23:59:59.000Z

131

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

132

Photochemistry of aromatic hydrocarbons: implications for ozone and secondary organic aerosol formation  

E-Print Network [OSTI]

formation is essential to assess the urban air pollution. This dissertation consists of two parts: (1) theoretical investigation of the toluene oxidation initiated by OH radical using quantum chemical and kinetic calculations to understand the mechanism of O...

Suh, Inseon

2006-08-16T23:59:59.000Z

133

Membrane separation of hydrocarbons using cycloparaffinic solvents  

DOE Patents [OSTI]

Heavy crude oils which contain metal contaminants such as nickel, vanadium and iron may be separated from light hydrocarbon oils by passing a solution of the crude oil dissolved in a cycloparaffinic hydrocarbon solvent containing from about 5 to about 8 carbon atoms by passing through a polymeric membrane which is capable of maintaining its integrity in the presence of hydrocarbon compounds. The light hydrocarbon oils which possess relatively low molecular weights will be recovered as the permeate while the heavy oils which possess relatively high molecular weights as well as the metal contaminants will be recovered as the retentate.

Kulkarni, Sudhir S. (Hoffman Estates, IL); Chang, Y. Alice (Westmont, IL); Gatsis, John G. (Des Plaines, IL); Funk, Edward W. (Highland Park, IL)

1988-01-01T23:59:59.000Z

134

Application of advanced hydrocarbon characterization and its...  

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

advanced hydrocarbon characterization and its consequences on future fuel properties and advanced combustion research Rafal Gieleciak, Craig Fairbridge and Darcy Hager Poster...

135

Membrane separation of hydrocarbons using cycloparaffinic solvents  

DOE Patents [OSTI]

Heavy crude oils which contain metal contaminants such as nickel, vanadium and iron may be separated from light hydrocarbon oils by passing a solution of the crude oil dissolved in a cycloparaffinic hydrocarbon solvent containing from about 5 to about 8 carbon atoms by passing through a polymeric membrane which is capable of maintaining its integrity in the presence of hydrocarbon compounds. The light hydrocarbon oils which possess relatively low molecular weights will be recovered as the permeate while the heavy oils which possess relatively high molecular weights as well as the metal contaminants will be recovered as the retentate.

Kulkarni, S.S.; Chang, Y.A.; Gatsis, J.G.; Funk, E.W.

1988-06-14T23:59:59.000Z

136

Nox reduction system utilizing pulsed hydrocarbon injection  

DOE Patents [OSTI]

Hydrocarbon co-reductants, such as diesel fuel, are added by pulsed injection to internal combustion engine exhaust to reduce exhaust NO.sub.x to N.sub.2 in the presence of a catalyst. Exhaust NO.sub.x reduction of at least 50% in the emissions is achieved with the addition of less than 5% fuel as a source of the hydrocarbon co-reductants. By means of pulsing the hydrocarbon flow, the amount of pulsed hydrocarbon vapor (itself a pollutant) can be minimized relative to the amount of NO.sub.x species removed.

Brusasco, Raymond M. (Livermore, CA); Penetrante, Bernardino M. (San Ramon, CA); Vogtlin, George E. (Fremont, CA); Merritt, Bernard T. (Livermore, CA)

2001-01-01T23:59:59.000Z

137

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

138

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

139

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

140

OXIDATION OF DRY HYDROCARBONS AT HIGH-POWER DENSITY ANODES  

SciTech Connect (OSTI)

This work builds upon discoveries by the University of Pennsylvania and others pertaining to the oxidation of dry hydrocarbon fuels in high temperature solid oxide fuel cells. The work reported here was restricted primarily to dry methane and confirms that YSZ-based cells, having ceria in the anode as a catalyst and copper in the anode as a current collector, can operate on dry methane for extended periods. Thirty-three lab-scale cells of various designs were fabricated and operated under a variety of conditions. The longest-lived cell gave stable performance on dry methane at 800 C for over 305 hours. Only slight carbon deposition was noted at the completion of the test. A corresponding nickel/YSZ-based anode would have lasted for less than an hour under these test conditions (which included open circuit potential measurements) before carbon fouling essentially destroyed the cell. The best performing cell achieved 112 mW/cm{sub 2} on dry methane at 800 C. Several problems were encountered with carbon fouling and declining open circuit voltages in many of the test cells after switching from operation on hydrogen to dry methane. Although not rigorously confirmed by experimentation, the results suggested that air infiltration through less than perfect perimeter seals or pinholes in the electrolytes, or both gave rise to conditions that caused the carbon fouling and OCV decline. Small amounts of air reacting with methane in a partial oxidation reaction could produce carbon monoxide that, in turn, would deposit the carbon. If this mechanism is confirmed, it implies that near perfect hardware is required for extended operation. Some evidence was also found for the formation of electrical shorts, probably from carbon deposits bridging the electrolyte. Work with odorized methane and with methane containing 100-ppm hydrogen sulfide confirmed that copper is stable at 800 C in dry hydrocarbon fuels in the presence of sulfur. In a number of cases, but not exclusively, the performance life on dry methane with sulfur compounds was much longer than with dry methane alone. The effect of sulfur compounds in these cases appeared to correlate with inhibition of carbon deposition. Mixed results were obtained for the effect of the sulfur compounds on power density. Progress also was made in understanding the mechanisms involved in direct utilization of dry natural gas. Evidence was developed for three possible mechanisms for dry methane utilization in addition to the usually cited mechanism--direct oxidation of methane by oxygen anions. Further work is required at a fundamental level before the knowledge gained here can be translated into higher levels of performance.

K.Krist; O. Spaldon-Stewart; R. Remick

2004-03-01T23:59:59.000Z

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

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

142

Southern Hemisphere Additional Ozonesondes (SHADOZ) 19982000 tropical ozone climatology  

E-Print Network [OSTI]

ozone record from Paramaribo, Surinam (6°N, 55°W) (also in SHADOZ) shows a marked contrast to southern tropical ozone because Surinam is often north of the Intertropical Convergence Zone (ITCZ). A more

Thompson, Anne

143

Concentration of ozone in surface air over greater Boston  

E-Print Network [OSTI]

Surface ozone concentrations were measured in the Greater Boston area from November, 1964 to December, 1965. Ozone was monitored continuosly using a Mast microcoulombmetric sensor. A chromium trioxide filter was fitted to ...

Widen, Donald Allen

1966-01-01T23:59:59.000Z

144

Polynuclear aromatic hydrocarbons for fullerene synthesis in flames  

DOE Patents [OSTI]

This invention provides improved methods for combustion synthesis of carbon nanomaterials, including fullerenes, employing multiple-ring aromatic hydrocarbon fuels selected for high carbon conversion to extractable fullerenes. The multiple-ring aromatic hydrocarbon fuels include those that contain polynuclear aromatic hydrocarbons. More specifically, multiple-ring aromatic hydrocarbon fuels contain a substantial amount of indene, methylnapthalenes or mixtures thereof. Coal tar and petroleum distillate fractions provide low cost hydrocarbon fuels containing polynuclear aromatic hydrocarbons, including without limitation, indene, methylnapthalenes or mixtures thereof.

Alford, J. Michael; Diener, Michael D.

2006-12-19T23:59:59.000Z

145

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

146

Hydrocarbon conversion process and catalysts  

SciTech Connect (OSTI)

This patent describes a process for hydrocracking hydrocarbon oils into products of lower average molecular weight and lower average boiling point. It comprises contacting hydrocarbon oil at a temperature between 250{sup 0}C and 500{sup 0}C and a pressure up to 300 bar in the presence of hydrogen with a catalyst consisting essentially of a Y zeolite modified to have a unit cell size below 24.40 A, a water adsorption capacity (at 25{sup 0}C and a rho/rho/sub o/ value of 0.2) of between 10% and 15% by weight of the zeolite and a pore volume of at least 0.25 ml/g wherein between 10% and 60% of the total pore volume is made up of pores having a diameter of at least 8 nm; am amorphous cracking component, a binder and at least one hydrogenation component selected from the group consisting of a Group VI metal, a Group VIII metal and mixtures thereof.

Hoek, A.; Huizinga, T.; Maxwell, I.E.

1989-08-15T23:59:59.000Z

147

Tensile Effective Stresses in Hydrocarbon Storage Caverns  

E-Print Network [OSTI]

Tensile Effective Stresses in Hydrocarbon Storage Caverns Hippolyte Djizanne and Pierre Bérest LMS, Germany,1-2 October 2012 TENSILE EFFECTIVE STRESSES IN HYDROCARBON STORAGE CAVERNS Hippolyte Djizanne1 that effective tensile stresses can be generated at a cavern wall after a rapid increase or decrease in pressure

Paris-Sud XI, Université de

148

Conversion of organic solids to hydrocarbons  

DOE Patents [OSTI]

A method of converting organic solids to liquid and gaseous hydrocarbons includes impregnating an organic solid with photosensitizing ions and exposing the impregnated solid to light in a non-oxidizing atmosphere for a time sufficient to photocatalytically reduce the solid to at least one of a liquid and a gaseous hydrocarbon.

Greenbaum, Elias (Oak Ridge, TN)

1995-01-01T23:59:59.000Z

149

Conversion of organic solids to hydrocarbons  

DOE Patents [OSTI]

A method of converting organic solids to liquid and gaseous hydrocarbons includes impregnating an organic solid with photosensitizing ions and exposing the impregnated solid to light in a non-oxidizing atmosphere for a time sufficient to photocatalytically reduce the solid to at least one of a liquid and a gaseous hydrocarbon. 5 Figs.

Greenbaum, E.

1995-05-23T23:59:59.000Z

150

The impact of interannual variability on multidecadal total ozone simulations  

E-Print Network [OSTI]

to reinforce the chemical ozone depletion caused by the enhanced aerosol loading following the eruption of Mt

Jackman, Charles H.

151

Ozone treatment in a closed culture system for Macrobrachium rosenbergii  

E-Print Network [OSTI]

constant flow of air. The Orthotoridine-Manganese Method (OTM) wss employed to measure ozone in solution (APHA, 1976) . Because of the rapid rate of decomposition of ozone in water, it was determined that the production of ozone could not be measured... by introducing into water and then sampling that water for analysis with OTM. Therefore, ozone was introduced directly into a solution of OTM reagent with subsequent changes in color of the reagent, measured on a "B & L Spectronic 70" spectrophotometer, being...

Yamaguchi, Ryoji

1978-01-01T23:59:59.000Z

152

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

153

Low-Temperature Hydrocarbon/CO Oxidation Catalysis in Support...  

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

& Publications Low-Temperature HydrocarbonCO Oxidation Catalysis in Support of HCCI Emission Control Low-Temperature HydrocarbonCO Oxidation Catalysis in Support of HCCI...

154

Commercialization of IH2® Biomass Direct-to-Hydrocarbon Fuel...  

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

Commercialization of IH2 Biomass Direct-to-Hydrocarbon Fuel Technology Commercialization of IH2 Biomass Direct-to-Hydrocarbon Fuel Technology Breakout Session 2: Frontiers and...

155

Cyclic process for producing methane from carbon monoxide with heat removal  

DOE Patents [OSTI]

Carbon monoxide-containing gas streams are converted to methane by a cyclic, essentially two-step process in which said carbon monoxide is disproportionated to form carbon dioxide and active surface carbon deposited on the surface of a catalyst, and said carbon is reacted with steam to form product methane and by-product carbon dioxide. The exothermic heat of reaction generated in each step is effectively removed during each complete cycle so as to avoid a build up of heat from cycle-to-cycle, with particularly advantageous techniques being employed for fixed bed, tubular and fluidized bed reactor operations.

Frost, Albert C. (Congers, NY); Yang, Chang-lee (Spring Valley, NY)

1982-01-01T23:59:59.000Z

156

A study of the effect of ozone and antioxidants on ozone-sensitive loblolly pine  

E-Print Network [OSTI]

and exposed to LSX ambient ozone for two months. Arrows indicate pestained SDS-PAGE molecular weight standards (kD) and Rubisco large subunit. Lane R = pure spinach Rubisco large subunit. Lanes 1 and 2 = control seedlings in the Ozoban study. Lanes 3 and 4... radicals are produced during normal metabolism when oxygen is reduced to water. Grimes et al. (1983) studied the products that form from ozone in cells and found no detectable superoxide radicals, leading them to propose that either ozone or hydroxyl...

Posey, Karen Lashea

1995-01-01T23:59:59.000Z

157

Ozone determination in different copying centers  

E-Print Network [OSTI]

&ixicolr&gi 1st ed. , New York. Hemisphere Publishing Corp, 1 987, ppl35-13(? 12. Menzel, D. B. : Toxicity of Ozone, Oxygen and Radiation. AI111 Rev. of Pharmacol. 1970; 10: 37&)-394. 13. Menzel, D. B. : Ozone: An overview of its toxicity in m;in . in...-Threshold Limit Values for Chemi?;il Substances and Physical Agents in the Work Environm?ni 1991-1992. Cincinnati, Ohio: ACGIH 1991 24. Wadden, R. A. , and P. A. Scheff: /ndoor At't Pollt&ttr ii l si ?d New York: John Wiley & Sons, inc. , 1983, ppl-5. 25...

Lai, Chen-Fu

1993-01-01T23:59:59.000Z

158

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

159

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

160

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

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

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

162

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

163

Attosecond Control of Electron Dynamics in Carbon Monoxide I. Znakovskaya,1  

E-Print Network [OSTI]

Attosecond Control of Electron Dynamics in Carbon Monoxide I. Znakovskaya,1 P. von den Hoff,2 S by manipulating the laser frequency, phase and polarization in closed loop experiments [1]. Control- faces in the observed control? We describe experiments, where control of electron dynamics in carbon

Kling, Matthias

164

Effects of exogenous carbon monoxide on radiation-induced bystander effect in zebrafish embryos in vivo  

E-Print Network [OSTI]

that the dose-response of radiation in the low-dose regime deviated from the LNT model. A notable example radiation are linearly proportional to the absorbed dose, evidence accumulated in the past decades showed as a pharmaceutical agent to release a low dose of exogenous carbon monoxide (CO) to attenuate the effect on bystander

Yu, K.N.

165

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 the projection of the jet mean velocity on the line of sight. As the jet rotates with the nucleus, the velocity, an interesting feature is to be noted. We have computed the mean photometric centre from the peak intensity

Demoulin, Pascal

166

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

167

Selective photooxidation of hydrocarbons in zeolites by oxygen  

DOE Patents [OSTI]

A selective photooxidation process for the conversion of hydrocarbon molecules to partially oxygenated derivatives, which comprises the steps of adsorbing a hydrocarbon and oxygen onto a dehydrated zeolite support matrix to form a hydrocarbon-oxygen contact pair, and subsequently exposing the hydrocarbon-oxygen contact pair to visible light, thereby forming a partially oxygenated derivative.

Frei, Heinz (Berkeley, CA); Blatter, Fritz (Berkeley, CA); Sun, Hai (Berkeley, CA)

1998-01-01T23:59:59.000Z

168

Nuclear conflict and ozone depletion Quick summary  

E-Print Network [OSTI]

Nuclear conflict and ozone depletion Quick summary o Regional nuclear war could cause global which traps pollutants o Nuclear weapons cause explosions, which then causes things around the vicinity to start burning, which in turn releases black carbon; it is not the nuclear material or fallout causing

Toohey, Darin W.

169

Water solubility data for 151 hydrocarbons  

SciTech Connect (OSTI)

The solubility of a hydrocarbon in water is important from both an environmental and a safety perspective. This information is required by engineers who design or operate stripping processes that remove hydrocarbons from air or water, or who must determine the amount of a hydrocarbon that has dissolved in water following a chemical spill. In particular, the water solubilities of paraffins are increasingly important because of more-stringent government regulations. Paraffins, along with naphthenes and aromatics, are the three major components of unrefined fuels. The water solubilities of 151 paraffins are listed in tables. The data are valid between 25 and 121 C, typical temperature in air- and steam-stripping operations. Also included is a correlation equation that allows users to estimate hydrocarbon solubilities above the given temperature range.

Yaws, C.L.; Pan, Xiang; Lin, Xiaoyin (Lamar Univ., Beaumont, TX (United States))

1993-02-01T23:59:59.000Z

170

Solubilization of petroleum hydrocarbons using biosurfactants  

E-Print Network [OSTI]

that bioavailability of the crude oil to the microorganisms limited the degradation rates (Mills, 1994). Preliminary experiments at our laboratories have also indicated enhanced solubilities of petroleum hydrocarbons due to the effects of biosurfactants (Kanga et al...

Kanga, Shahrukh

1995-01-01T23:59:59.000Z

171

Removal of trace olefins from aromatic hydrocarbons  

SciTech Connect (OSTI)

A process is described for treating a hydrocarbon process stream by converting trace quantities of olefinic impurities to nonolefinic hydrocarbons. The process comprises contacting the process stream, which contains trace olefins in an amount of from about 50 to about 2000 as measured by Bromine Index and at least 80% by weight of aromatic and naphthenic hydrocarbons having from 6 to 20 carbon atoms per molecule, at reaction conditions which ensure liquid phase operation with a solid catalyst composite comprising a crystalline aluminosilicate zeolite and a refractory inorganic oxide. A catalytic olefin-consuming alkylation reaction then produces an essentially olefinfree product stream with approximately the same quantity and distribution of aromatic and naphthenic hydrocarbons as contained in the process stream.

Sachtler, J.W.A.; Barger, P.T.

1989-01-03T23:59:59.000Z

172

E-Print Network 3.0 - aromatic hydrocarbons estimated Sample...  

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

Geosciences 26 2006-01-0201 Speciated Hydrocarbon Emissions from an Automotive Diesel Summary: estimated for many hydrocarbons 26, 27. The MIR of a hydrocarbon is the...

173

E-Print Network 3.0 - aromatic hydrocarbons investigated Sample...  

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

compounds with two multiple-ringed polynuclear aromatic hydrocarbons (PAHs) or naphthenic hydrocarbons... Prediction of hydrocarbon molecular structure using infrared, Raman,...

174

E-Print Network 3.0 - aromatic hydrocarbon investigation Sample...  

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

compounds with two multiple-ringed polynuclear aromatic hydrocarbons (PAHs) or naphthenic hydrocarbons... Prediction of hydrocarbon molecular structure using infrared, Raman,...

175

E-Print Network 3.0 - aromatic hydrocarbons evaluated Sample...  

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

compounds with two multiple-ringed polynuclear aromatic hydrocarbons (PAHs) or naphthenic hydrocarbons... Prediction of hydrocarbon molecular structure using infrared, Raman,...

176

E-Print Network 3.0 - aromatic hydrocarbon diol-epoxide Sample...  

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

compounds with two multiple-ringed polynuclear aromatic hydrocarbons (PAHs) or naphthenic hydrocarbons... Prediction of hydrocarbon molecular structure using infrared, Raman,...

177

E-Print Network 3.0 - aromatic hydrocarbon residues Sample Search...  

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

compounds with two multiple-ringed polynuclear aromatic hydrocarbons (PAHs) or naphthenic hydrocarbons... Prediction of hydrocarbon molecular structure using infrared, Raman,...

178

E-Print Network 3.0 - aromatic hydrocarbons analyses Sample Search...  

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

compounds with two multiple-ringed polynuclear aromatic hydrocarbons (PAHs) or naphthenic hydrocarbons... Prediction of hydrocarbon molecular structure using infrared, Raman,...

179

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

E-Print Network [OSTI]

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

180

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

E-Print Network [OSTI]

Satellite observations of ozone and nitrogen dioxide: from retrievals to emission estimates #12 Satellite observations of ozone and nitrogen dioxide: from retrievals to emission es- timates / by Bas Subject headings: satellite retrieval / nitrogen dioxide / ozone / air pollution / emis- sion estimates

Haak, Hein

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

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

E-Print Network [OSTI]

inhibitor line Ozone Generator Oxygen Concentrator CellSequal oxygen concentrator and Pure-O-Tech ozone generator.This oxygen is then supplied into the ozone generator for

Aydogan, Ahmet

2006-01-01T23:59:59.000Z

182

A Study of Vibrational Relaxation of B-State Carbon Monoxide in the Heme Pocket of Photolyzed Carboxymyoglobin  

E-Print Network [OSTI]

, Massachusetts 02215 ABSTRACT The vibrational energy relaxation of dissociated carbon monoxide in the heme pocket for the two CO substate frequencies, T1(B1) 335 115 ps and T1(B2) 330 145 ps. These simulation results

Straub, John E.

183

Top-down estimate of a large source of atmospheric carbon monoxide associated with fuel combustion in Asia  

E-Print Network [OSTI]

modeling methodology, we find that the source of carbon monoxide from fossil-fuel and biofuel combustion-fuel and- biofuel combustion sources in North America, Europe, Asia (including Indonesia and the Middle

Palmer, Paul

184

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.

185

Ozone Removal by Filters Containing Activated Carbon: A Pilot Study  

SciTech Connect (OSTI)

This study evaluated the ozone removal performance of moderate-cost particle filters containing activated carbon when installed in a commercial building heating, ventilating, and air conditioning (HVAC) system. Filters containing 300 g of activated carbon per 0.09 m2 of filter face area were installed in two 'experimental' filter banks within an office building located in Sacramento, CA. The ozone removal performance of the filters was assessed through periodic measurements of ozone concentrations in the air upstream and downstream of the filters. Ozone concentrations were also measured upstream and downstream of a 'reference' filter bank containing filters without any activated carbon. The filter banks with prefilters containing activated carbon were removing 60percent to 70percent of the ozone 67 and 81 days after filter installation. In contrast, there was negligible ozone removal by the reference filter bank without activated carbon.

Fisk, William; Spears, Mike; Sullivan, Douglas; Mendell, Mark

2009-09-01T23:59:59.000Z

186

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

187

airborne antarctic ozone: Topics by E-print Network  

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

winter weather conditions: Severe cold and isolated air ow: circumpolar vortex North pole vortex breakdown replenishes ozone layer from outside: mixes air 12; E11;ects...

188

antarctic ozone recovery: Topics by E-print Network  

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

winter weather conditions: Severe cold and isolated air ow: circumpolar vortex North pole vortex breakdown replenishes ozone layer from outside: mixes air 12; E11;ects...

189

antarctic ozone hole: Topics by E-print Network  

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

winter weather conditions: Severe cold and isolated air ow: circumpolar vortex North pole vortex breakdown replenishes ozone layer from outside: mixes air 12; E11;ects...

190

antarctic ozone experiment: Topics by E-print Network  

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

winter weather conditions: Severe cold and isolated air ow: circumpolar vortex North pole vortex breakdown replenishes ozone layer from outside: mixes air 12; E11;ects...

191

antarctic ozone depletion: Topics by E-print Network  

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

winter weather conditions: Severe cold and isolated air ow: circumpolar vortex North pole vortex breakdown replenishes ozone layer from outside: mixes air 12; E11;ects...

192

Exposure-Relevant Ozone Chemistry in Occupied Spaces  

E-Print Network [OSTI]

from the material balance on ozone (equation 4-1). S [O 3 ](equation 5-2, which reflects a steady-state material balance

Coleman, Beverly Kaye

2009-01-01T23:59:59.000Z

193

Ozone heating and the destabilization of traveling waves during summer  

SciTech Connect (OSTI)

The effects of ozone heating on the linear stability of lower stratospheric traveling waves of the summertime, extratropical circulation are examined. Based on coupled equations for the quasigeostrophic potential vorticity and ozone volume mixing ratio, it is shown that the diabatic heating arising from ozone advection can offset the damping due to Newtonian cooling, leading to wave amplification and significant changes in the structure and zonally rectified fluxes of the wave fields in both the lower stratosphere and troposphere. The vertical profile of the zonal mean wind plays a crucial role in determining whether the ozone heating destabilizes eastward and/or westward traveling disturbances.

Nathan, T.R.; Cordero, E.C.; Li, L. [Univ. of California, Davis, CA (United States)] [Univ. of California, Davis, CA (United States)

1994-07-01T23:59:59.000Z

194

Syngas Upgrading to Hydrocarbon Fuels Technology Pathway  

SciTech Connect (OSTI)

In support of the Bioenergy Technologies Office, the National Renewable Energy Laboratory (NREL) and the Pacific Northwest National Laboratory (PNNL) are undertaking studies of biomass conversion technologies to hydrocarbon fuels to identify barriers and target research toward reducing conversion costs. Process designs and preliminary economic estimates for each of these pathway cases were developed using rigorous modeling tools (Aspen Plus and Chemcad). These analyses incorporated the best information available at the time of development, including data from recent pilot and bench-scale demonstrations, collaborative industrial and academic partners, and published literature and patents. This pathway case investigates the upgrading of biomass derived synthesis gas (‘syngas’) to hydrocarbon biofuels. While this specific discussion focuses on the conversion of syngas via a methanol intermediate to hydrocarbon blendstocks, there are a number of alternative conversion routes for production of hydrocarbons through a wide array of intermediates from syngas. Future work will also consider the variations to this pathway to determine the most economically viable and risk adverse conversion route. Technical barriers and key research needs have been identified that should be pursued for the syngas to hydrocarbon pathway to be competitive with petroleum-derived gasoline, diesel and jet range blendstocks.

Talmadge, M.; Biddy, Mary J.; Dutta, Abhijit; Jones, Susanne B.; Meyer, Pimphan A.

2013-03-31T23:59:59.000Z

195

E-Print Network 3.0 - ambient ozone levels Sample Search Results  

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

level ozone. Lesson 2: Ozone Formation... , power plants and industry all emit air pollution that forms ... Source: Royer, Dana - Department of Earth and Environmental Sciences,...

196

E-Print Network 3.0 - ash ozonation technology Sample Search...  

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

ozonation technology Search Powered by Explorit Topic List Advanced Search Sample search results for: ash ozonation technology Page: << < 1 2 3 4 5 > >> 1 Fine volcanic Predicting...

197

E-Print Network 3.0 - ambient ozone growth Sample Search Results  

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

Climate and Environment (Climate) Impacts of ozone on trees and crops Summary: and carbon sequestration. Vegetation exposure to ozone reduces photosynthesis, growth, and...

198

Final Report, "Molecular Design of Hydrocarbon Oxidation Catalytic Processes"  

SciTech Connect (OSTI)

The main goal of this project had been to use model systems to correlate selectivities in partial oxidation catalysis with the presence of specific sites on the surface of the catalyst. Extensive work was performed this year on characterizing oxygen-treated nickel surfaces by chemical means. Specifically, the surface chemistry of ammonia coadsorbed with atomic oxygen on Ni(110) single-crystal surfaces was studied by temperature-programmed desorption (TPD) and X-ray photoelectron spectroscopy (XPS). It was determined that at intermediate oxygen coverages direct ammonia adsorption on nickel sites is suppressed, but a new high-temperature reaction regime is generated at 400 K where NHx surface fragments are rehydrogenated concurrently with the production of water and molecular hydrogen. The extensive isotope scrambling and hydrogen transfer seen from nitrogen- to oxygen-containing surface intermediates, and the optimum yields seen for this 400 K state at intermediate oxygen coverages, strongly suggest the direct interaction of the adsorbed ammonia with oxygen atoms at the end of the –Ni–O- rows that form upon reconstruction of the surface. Hydrogen transfer between ammonia and oxygen appears to take place directly via hydrogen bonding, and to be reversible but biased towards water formation. An equilibrium is reached between the produced water and the reacting surface oxygen and hydrogen. The strong influence of the OH surface groups on the thermal chemistry of the adsorbed ammonia was interpreted in terms of the adsorbing geometry of the OH groups on the surface, and of hydrogen bonding between adsorbed OH and NH3 species. In terms of alcohol reactivity, the adsorption of 2-iodoethanol, a precursor for the preparation of 2-hydroxyethyl and oxametallacycle surface species, was found to lead to two configurations involving either just the iodine atom or both iodine and hydroxyl ends of the molecule. A complex chemical behavior starts around 140 K with the production of small amounts of ethylene and water, most likely via the concerted decomposition or disproportionation of the adsorbed molecular species. The bulk of the 2-iodoethanol decomposes at about 150 K via an initial carbon-iodine scission to form –O(H)CH2CH2– (~80%) and 2-hydroxyethyl (~20%) intermediates. Two competing reactions are involved with the subsequent conversion of the 2-hydroxyethyl species around 160 K, a reductive elimination with surface hydrogen to yield ethanol, and a ?-H elimination to surface vinyl alcohol. The –O(H)CH2CH2–, on the other hand, dehydrogenates to a –OCH2CH2– oxametallacycle species about the same temperature. Both 2-hydroxyethyl and oxametallacycle species tautomerize to acetaldehyde, around 210 K and above 250 K, respectively, and some of that acetaldehyde desorbs while the rest decomposes to hydrogen and carbon monoxide. We contend that a better understanding of the surface chemistry of oxygen-containing surfaces can lead to better selectivities in catalysis. This is arguably the most important issue in the field of catalysis in the near future, and one that impacts several technologies of interest to DOE such as the manufacturing of speciality chemicals and the control and removal of pollutants. Additional work was performed on the characterization of the chemistry of methyl and methylene adsorbed species on oxygen-treated nickel surfaces. Complex chemistry was observed involving not only hydrogenation and dehydrogenation steps, but also C-C couplings and methylene insertions to produce heavier hydrocarbons, and oxygen insertion reactions that yield oxygenates. Finally, a dual titration technique employing xenon and a chemically sensitive probe was developed to identify minority catalytic sites on oxide surfaces. In the case of oxygen-treated Ni(110) single crystals, it was found that both hydrogen transfer with adsorbed water or ammonia and certain hydrocarbon hydrogenation reactions take place at the end of the –Ni–O rows that form in this system. Carbon and nitrogen oxides, on the other hand, display no pre

Professor Francisco Zaera

2007-08-09T23:59:59.000Z

199

Using supercritical fluids to refine hydrocarbons  

DOE Patents [OSTI]

This is a method to reactively refine hydrocarbons, such as heavy oils with API gravities of less than 20.degree. and bitumen-like hydrocarbons with viscosities greater than 1000 cp at standard temperature and pressure using a selected fluid at supercritical conditions. The reaction portion of the method delivers lighter weight, more volatile hydrocarbons to an attached contacting device that operates in mixed subcritical or supercritical modes. This separates the reaction products into portions that are viable for use or sale without further conventional refining and hydro-processing techniques. This method produces valuable products with fewer processing steps, lower costs, increased worker safety due to less processing and handling, allow greater opportunity for new oil field development and subsequent positive economic impact, reduce related carbon dioxide, and wastes typical with conventional refineries.

Yarbro, Stephen Lee

2014-11-25T23:59:59.000Z

200

Catalysts for synthesizing various short chain hydrocarbons  

DOE Patents [OSTI]

Method and apparatus (10), including novel photocatalysts, are disclosed for the synthesis of various short chain hydrocarbons. Light-transparent SiO.sub.2 aerogels doped with photochemically active uranyl ions (18) are fluidized in a fluidized-bed reactor (12) having a transparent window (16), by hydrogen and CO, C.sub.2 H.sub.4 or C.sub.2 H.sub.6 gas mixtures (20), and exposed to radiation (34) from a light source (32) external to the reactor (12), to produce the short chain hydrocarbons (36).

Colmenares, Carlos (Alamo, CA)

1991-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

Conversion of methane and acetylene into gasoline range hydrocarbons  

E-Print Network [OSTI]

Conversion of methane and acetylene to higher molecular weight hydrocarbons over zeolite catalyst (HZSM-5) was studied The reaction between methane and acetylene successfully produced high molecular weight hydrocarbons, such as naphthalene, benzene...

Alkhawaldeh, Ammar

2000-01-01T23:59:59.000Z

202

Seismic Analysis Using Wavelet Transform for Hydrocarbon Detection  

E-Print Network [OSTI]

result in successful hydrocarbon finds because abnormal seismic amplitude variations can sometimes be caused by other factors, such as alternative lithology and residual hydrocarbons in certain depositional environments. Furthermore, not all gas fields...

Cai, Rui

2012-02-14T23:59:59.000Z

203

Chemical nature of high-molecular hydrocarbons of gaseous condensates  

SciTech Connect (OSTI)

Mass spectrometry was used to study the group-structure composition of high-boiling 50 deg (200/degrees/-250/degrees/, 250/degrees/-300/degrees/, and 300/degrees/-350/degrees/C) fractions of East Turkmenistan condensates: the hydrocarbons composition is characterized by a high content of paraffinic hydrocarbons, and that of others by aromatic and naphthenic hydrocarbons. For all the condensates under investigation, as the boiling temperature of fractions increases, the content of paraffinic hydrocarbons in them is increased, while that of naphthenic hydrocarbons is reduced. The distribution of naphthenic hydrocarbons according to the number of rings is identical. In high-paraffin condensates, monoaromatic hydrocarbons consist mainly structures with alkyl substituents, but in condensates with a high content of aromatic and naphthenic hydrocarbons they consist mainly of structures with naphthenic substituents. 4 references, 1 figures, 2 tables.

Kul'dzhayev, B.A.; Makarov, V.V.; Sergiyenko, S.R.; Khramova, E.V.

1987-01-01T23:59:59.000Z

204

Sustainable treatment of hydrocarbon-contaminated industrial land   

E-Print Network [OSTI]

Land contamination by petroleum hydrocarbons is a widespread and global environmental pollution issue from recovery and refining of crude oil and the ubiquitous use of hydrocarbons in industrial processes and applications. ...

Cunningham, Colin John

2012-06-25T23:59:59.000Z

205

A Parametric Study of the Effect of Temperature and Hydrocarbon...  

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

of Temperature and Hydrocarbon Species on the Product Distribution from a Non-Thermal Plasma Reactor A Parametric Study of the Effect of Temperature and Hydrocarbon Species on the...

206

E-Print Network 3.0 - aromatic hydrocarbons fluorene Sample Search...  

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

Hydrocarbons... Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous organic pollutants in urban environments... in the urbanized and rapidly urbanizing areas. Keywords...

207

E-Print Network 3.0 - aromatic hydrocarbon phenanthrene Sample...  

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

Abstract Polycyclic aromatic hydrocarbons (PAHs) and dioxins are lipophilic organic pollutants occurring... absorption, pig INTRODUCTION Polycyclic aromatic hydrocarbons (PAHs)...

208

E-Print Network 3.0 - aromatic hydrocarbons based Sample Search...  

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

Aromatic Hydrocarbons Volatile Organic... Compounds Toxic Organic Halogenated Dioxins Furans (dioxins) Polycyclic Aromatic Hydrocarbons found... Rana Novini ATOC 3500 Burn...

209

E-Print Network 3.0 - aromatic hydrocarbons Sample Search Results  

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

Hydrocarbons... Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous organic pollutants in urban environments... in the urbanized and rapidly urbanizing areas. Keywords...

210

E-Print Network 3.0 - aromatic hydrocarbons pah5 Sample Search...  

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

hydrocarbons (PAHs) are ubiquitous, recalcitrant, and potentially carcinogenic pollutants. Plants Summary: 1461 Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous,...

211

E-Print Network 3.0 - aromatic hydrocarbons inenvironmental Sample...  

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

Hydrocarbons... Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous organic pollutants in urban environments... in the urbanized and rapidly urbanizing areas. Keywords...

212

E-Print Network 3.0 - aromatic hydrocarbon o-quinones Sample...  

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

Hydrocarbons... Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous organic pollutants in urban environments... in the urbanized and rapidly urbanizing areas. Keywords...

213

E-Print Network 3.0 - aromatic hydrocarbons assessment Sample...  

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

Aromatic Hydrocarbons Volatile Organic... Compounds Toxic Organic Halogenated Dioxins Furans (dioxins) Polycyclic Aromatic Hydrocarbons found... of airborne soot. The air...

214

Method and apparatus for low temperature destruction of halogenated hydrocarbons  

DOE Patents [OSTI]

A method and apparatus for decomposing halogenated hydrocarbons are provided. The halogenated hydrocarbon is mixed with solvating agents and maintained in a predetermined atmosphere and at a predetermined temperature. The mixture is contacted with recyclable reactive material for chemically reacting with the recyclable material to create dehalogenated hydrocarbons and halogenated inorganic compounds. A feature of the invention is that the process enables low temperature destruction of halogenated hydrocarbons.

Reagen, William Kevin (Stillwater, MN); Janikowski, Stuart Kevin (Idaho Falls, ID)

1999-01-01T23:59:59.000Z

215

aromatic hydrocarbons coated: Topics by E-print Network  

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

Summary: ??Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous environmental pollutants, known human lung carcinogens, and potent mammary carcinogens in animal models....

216

Biological Conversion of Sugars to Hydrocarbons Technology Pathway  

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

Enzymes Acid + Caustic Wastewater Treatment Process Heat and Power Integration Biogas + Sludge Fuel Finishing (hydroprocessing, as needed) Electricity Hydrogen Hydrocarbon...

217

ORIGINAL CONTRIBUTION Ozone and Short-term Mortality  

E-Print Network [OSTI]

. With the National Morbidity, Mortality, and Air Pollution Study (NMMAPS), we have developed na- tional approaches Ambient Air Qual- ity Standard (NAAQS) for ozone, adding a daily maximum 8-hour stan- dard of 80 ppb.19 Because of the relevance of epidemiologic evi- dence to the NAAQS for ozone and other pollutants

Dominici, Francesca

218

Atmospheric Environment 41 (2007) 31513160 Ozone removal by HVAC filters  

E-Print Network [OSTI]

Atmospheric Environment 41 (2007) 3151­3160 Ozone removal by HVAC filters P. Zhao, J.A. Siegel�, R May 2006; accepted 14 June 2006 Abstract Residential and commercial HVAC filters that have been loaded of the relative importance of HVAC filters as a removal mechanism for ozone in residential and commercial

Siegel, Jeffrey

219

Proceedings: Indoor Air 2005 OZONE REMOVAL BY RESIDENTIAL HVAC FILTERS  

E-Print Network [OSTI]

Proceedings: Indoor Air 2005 2366 OZONE REMOVAL BY RESIDENTIAL HVAC FILTERS P Zhao1,2 , JA Siegel1, Austin, Texas 78758, USA ABSTRACT HVAC filters have a significant influence on indoor air quality% for Filter #2 at a face velocity of 0.81 cm/s. The potential for HVAC filters to affect ozone concentrations

Siegel, Jeffrey

220

URBAN OZONE CONCENTRATION FORECASTING WITH ARTIFICIAL NEURAL NETWORK IN CORSICA  

E-Print Network [OSTI]

Perceptron; Ozone concentration. 1. Introduction Tropospheric ozone is a major air pollution problem, both, Ajaccio, France, e-mail: balu@univ-corse.fr Abstract: Atmospheric pollutants concentration forecasting is an important issue in air quality monitoring. Qualitair Corse, the organization responsible for monitoring air

Boyer, Edmond

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

Production of hydrocarbons from hydrates. [DOE patent application  

DOE Patents [OSTI]

An economical and safe method of producing hydrocarbons (or natural gas) from in situ hydrocarbon-containing hydrates is given. Once started, the method will be self-driven and will continue producing hydrocarbons over an extended period of time (i.e., many days).

McGuire, P.L.

1981-09-08T23:59:59.000Z

222

Method for removing chlorine compounds from hydrocarbon mixtures  

DOE Patents [OSTI]

A process for removing halide ions from a hydrocarbon feedstream containing halogenated hydrocarbons wherein the contaminated feedstock is contacted with a solution of a suitable oxidizing acid containing a lanthanide oxide, the acid being present in a concentration of at least about 50 weight percent for a time sufficient to remove substantially all of the halide ion from the hydrocarbon feedstock.

Janoski, E.J.; Hollstein, E.J.

1984-09-29T23:59:59.000Z

223

Substantially self-powered method and apparatus for recovering hydrocarbons from hydrocarbon-containing solid hydrates  

DOE Patents [OSTI]

A method and apparatus are provided for producing gaseous hydrocarbons from formations comprising solid hydrocarbon hydrates located under either a body of land or a body of water. The vast natural resources of such hydrocarbon hydrates can thus now be economically mined. Relatively warm brine or water is brought down from an elevation above that of the hydrates through a portion of the apparatus, and passes in contact with the hydrates, thus melting them. The liquid then continues up another portion of the apparatus carrying entrained hydrocarbon vapors in the form of bubbles, which can easily be separated from the liquid. After a short startup procedure, the process and apparatus are substantially self-powered.

Elliott, G.R.B.; Barraclough, B.L.; Vanderborgh, N.E.

1981-02-19T23:59:59.000Z

224

Substantially self-powered method and apparatus for recovering hydrocarbons from hydrocarbon-containing solid hydrates  

DOE Patents [OSTI]

A method and apparatus are provided for producing gaseous hydrocarbons from formations comprising solid hydrocarbon hydrates located under either a body of land or a body of water. The vast natural resources of such hydrocarbon hydrates can thus now be economically mined. Relatively warm brine or water is brought down from an elevation above that of the hydrates through a portion of the apparatus and passes in contact with the hydrates, thus melting them. The liquid then continues up another portion of the apparatus, carrying entrained hydrocarbon vapors in the form of bubbles, which can easily be separated from the liquid. After a short startup procedure, the process and apparatus are substantially self-powered.

Elliott, Guy R. B. (Los Alamos, NM); Barraclough, Bruce L. (Santa Fe, NM); Vanderborgh, Nicholas E. (Los Alamos, NM)

1983-01-01T23:59:59.000Z

225

Apparatus for recovering gaseous hydrocarbons from hydrocarbon-containing solid hydrates  

DOE Patents [OSTI]

A method and apparatus are provided for producing gaseous hydrocarbons from formations comprising solid hydrocarbon hydrates located under either a body of land or a body of water. The vast natural resources of such hydrocarbon hydrates can thus now be economically mined. Relatively warm brine or water is brought down from an elevation above that of the hydrates through a portion of the apparatus and passes in contact with the hydrates, thus melting them. The liquid then continues up another portion of the apparatus, carrying entrained hydrocarbon vapors in the form of bubbles, which can easily be separated from the liquid. After a short startup procedure, the process and apparatus are substantially self-powered.

Elliott, Guy R. B. (Los Alamos, NM); Barraclough, Bruce L. (Santa Fe, NM); Vanderborgh, Nicholas E. (Los Alamos, NM)

1984-01-01T23:59:59.000Z

226

Method of dispersing a hydrocarbon using bacteria  

DOE Patents [OSTI]

New protozoan derived microbial consortia and method for their isolation are provided. Consortia and bacteria isolated therefrom are useful for treating wastes such as trichloroethylene and trinitrotoluene. Consortia, bacteria isolated therefrom, and dispersants isolated therefrom are useful for dispersing hydrocarbons such as oil, creosote, wax, and grease.

Tyndall, Richard L. (Clinton, TN)

1996-01-01T23:59:59.000Z

227

Mass Transfer of Polynuclear Aromatic Hydrocarbons from  

E-Print Network [OSTI]

of the individual components of four synthetic dense non-aqueous phase liquid (DNAPL) mixtures into the aqueous hydrocarbons (PAHs), were designed to serve as models for coal tars and creosotes. The reactor employed (PAHs) are often present in the environment as components of such dense non- aqueous phase liquids

Peters, Catherine A.

228

Use of Advanced Oxidation and Aerobic Degradation for Remediation of Various Hydrocarbon Contaminates  

SciTech Connect (OSTI)

Western Research Institute in conjunction with Sierra West Consultants, Inc., Tetra Tech, Inc., and the U.S. Department of Energy conducted laboratory and field studies to test different approaches to enhance degradation of hydrocarbons and associated contaminants. WRI in conjunction with Sierra West Consultants, Inc., conducted a laboratory and field study for using ozone to treat a site contaminated with MTBE and other hydrocarbons. Results from this study demonstrate that a TOD test can be used to resolve the O{sub 3} dosage problem by establishing a site-specific benchmark dosage for field ozone applications. The follow-up testing of the laboratory samples provided indications that intrinsic biodegradation could be stimulated by adding oxygen. Laboratory studies also suggests that O3 dosage in the full-scale field implementation could be dialed lower than stoichiometrically designed to eliminate the formation of Cr(VI). WRI conducted a study involving a series of different ISCO oxidant applications to diesel-contaminated soil and determined the effects on enhancing biodegradation to degrade the residual hydrocarbons. Soils treated with permanganate followed by nutrients and with persulfate followed by nutrients resulted in the largest decrease in TPH. The possible intermediates and conditions formed from NOM and TPH oxidation by permanganate and activated persulfate favors microbial TPH degrading activity. A 'passive-oxidation' method using microbial fuel cell (MFC) technology was conducted by WRI in conjunction with Tetra Tech, Inc., to degrade MTBE in groundwater. These experiments have demonstrated that a working MFC (i.e., one generating power) could be established in the laboratory using contaminated site water or buffered media inoculated with site water and spiked with MTBE, benzene, or toluene. Electrochemical methods were studied by WRI with goal of utilizing low voltage and amperage electrical sources for 'geo-oxidation' of organic contaminants. The results from a study with TCE contaminated-clay indicate that electrochemically inducing reductive dechlorination of TCE in a saturated matrix may offer an effective and viable alternative to remediation TCE and other contaminants with potential of being reduced. Another study focused on steel wool oxidation to electrochemically increase population of hydrocarbon-degrading denitrifying bacteria. Significantly larger denitrifying activity was observed in the cathode chamber of a treatment unit setup like an MFC with steel wool as the anode. This enhanced nitrate reduction could be due to direct electron utilization by denitrifying bacteria on the cathode, thereby stimulating microbial denitrification or a combination of electron transfer directly to NO{sub 3}{sup -} and electron transfer to nitrate reducing bacteria, which may serve as a type of bio-catalyst on the cathode for nitrate reduction. Overall, the studies conducted under Task 72 demonstrated different innovative methods to enhance petroleum hydrocarbon degradation and associated contaminants.

Paul Fallgren

2009-03-06T23:59:59.000Z

229

Effects of 20002050 changes in climate and emissions on global tropospheric ozone and the policy-relevant background surface ozone  

E-Print Network [OSTI]

) project major changes in anthro- pogenic emissions of greenhouse gases and ozone precur- sors over the 2Effects of 2000­2050 changes in climate and emissions on global tropospheric ozone and the policy; published 27 September 2008. [1] We use a global chemical transport model (GEOS-Chem) driven by a general

Mickley, Loretta J.

230

Proceedings: Indoor Air 2005 REACTIONS BETWEEN OZONE AND BUILDING PRODUCTS: IMPACT ON  

E-Print Network [OSTI]

Proceedings: Indoor Air 2005 2118 REACTIONS BETWEEN OZONE AND BUILDING PRODUCTS: IMPACT ON PRIMARY of reactions of ozone on building products and on their emissions in indoor air. For this purpose, 12 building products were exposed to ozone in a dedicated experimental setup. The measured ozone removal rate

Paris-Sud XI, Université de

231

Ozone ensemble forecast with machine learning Vivien Mallet,1,2  

E-Print Network [OSTI]

Ozone ensemble forecast with machine learning algorithms Vivien Mallet,1,2 Gilles Stoltz,3 forecasts. The latter rely on a multimodel ensemble built for ozone forecasting with the modeling system Europe in order to forecast ozone daily peaks and ozone hourly concentrations. On the basis of past

Paris-Sud XI, Université de

232

An ozone climatology of the Dallas-Fort Worth area and its relationship to meteorology  

E-Print Network [OSTI]

, no extensive studies on ozone in this area have been published. This study presents a broad overview of the ozone problem in the DFW area. An ozone spatial and temporal climatology was constructed using ozone data at 23 different monitoring sites from 1980...

Nobis, Timothy Edward

1998-01-01T23:59:59.000Z

233

Hydrocarbon composition of crude oils near the Caspian depression  

SciTech Connect (OSTI)

The structural-group composition of hydrocarbons of Mesozoic crude oils near the Caspian depression was investigated by mass-spectrometry, followed by the analysis of the mass-spectra using a computer. The distribution of naphthenic hydrocarbons, according to the number of rings and of aromatic hydrocarbons, according to the degree of hydrogen unsaturation is similar for all the crude oils examined. The hydrocarbon composition of Mesozoic crude oils is characterized by a reduction in the content of aliphatic hydrocarbons and alkyl benzenes.

Botneva, T.A.; Khramova, E.V.; Nekhamkina, L.G.; Polyakova, A.A.

1983-01-01T23:59:59.000Z

234

Composition of paraffinic and naphthenic hydrocarbons in petroleum asphalts  

SciTech Connect (OSTI)

Uses a combination of chromatographic, chemical, and spectroscopic methods to determine the composition of the paraffinic and naphthenic hydrocarbons recovered from asphalts. Monitors the completeness of separation of the hydrocarbons from the aromatics on the basis of UV spectra. Finds that in the mixture of adduct-forming hydrocarbons, along with the n-paraffins there were admixtures of isoparaffins and longchain alkylnaphthenes. Concludes that a comparison of the structural-group composition of the asphalt fractions from the different crudes shows that there are only slight differences in the structure of the paraffinic/naphthenic hydrocarbons present in these asphalts, particularly with regard to those hydrocarbons that do not react with urea.

Botvin'eva, A.M.; Dubkova, R.V.; Shkredova, N.A.

1982-11-01T23:59:59.000Z

235

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

236

Plasma-assisted conversion of solid hydrocarbon to diamond  

DOE Patents [OSTI]

A process of preparing diamond, e.g., diamond fiber, by subjecting a hydrocarbon material, e.g., a hydrocarbon fiber, to a plasma treatment in a gaseous feedstream for a sufficient period of time to form diamond, e.g., a diamond fiber is disclosed. The method generally further involves pretreating the hydrocarbon material prior to treatment with the plasma by heating within an oxygen-containing atmosphere at temperatures sufficient to increase crosslinking within said hydrocarbon material, but at temperatures insufficient to melt or decompose said hydrocarbon material, followed by heating at temperatures sufficient to promote outgassing of said crosslinked hydrocarbon material, but at temperatures insufficient to convert said hydrocarbon material to carbon.

Valone, Steven M. (Santa Fe, NM); Pattillo, Stevan G. (Los Alamos, NM); Trkula, Mitchell (Los Alamos, NM); Coates, Don M. (Santa Fe, NM); Shah, S. Ismat (Wilmington, DE)

1996-01-01T23:59:59.000Z

237

Nonadiabatic calculations of ultraviolet absorption cross section of sulfur monoxide: Isotopic effects on the photodissociation reaction  

SciTech Connect (OSTI)

Ultraviolet absorption cross sections of the main and substituted sulfur monoxide (SO) isotopologues were calculated using R-Matrix expansion technique. Energies, transition dipole moments, and nonadiabatic coupling matrix elements were calculated at MRCI/AV6Z level. The calculated absorption cross section of {sup 32}S{sup 16}O was compared with experimental spectrum; the spectral feature and the absolute value of photoabsorption cross sections are in good agreement. Our calculation predicts a long lived photoexcited SO* species which causes large non-mass dependent isotopic effects depending on the excitation energy in the ultraviolet region.

Danielache, Sebastian O.; Tomoya, Suzuki; Nanbu, Shinkoh [Department of Materials and Life Sciences, Faculty of Science and Technology, Sophia University, Chiyoda Ku, Tokyo 102-8554 (Japan)] [Department of Materials and Life Sciences, Faculty of Science and Technology, Sophia University, Chiyoda Ku, Tokyo 102-8554 (Japan); Kondorsky, Alexey [P. N. Lebedev Physical Institute of Russian Academy of Science, Leninsky pr., 53, Moscow, 119991 (Russian Federation) [P. N. Lebedev Physical Institute of Russian Academy of Science, Leninsky pr., 53, Moscow, 119991 (Russian Federation); Moscow Institute of Physics and Technology (State University), Institutsky per., 9, Dolgoprudny Moscow region, 141700 (Russian Federation); Tokue, Ikuo [Department of Chemistry, Faculty of Science, Niigata University, Ikarashi, Niigata 950-2181 (Japan)] [Department of Chemistry, Faculty of Science, Niigata University, Ikarashi, Niigata 950-2181 (Japan)

2014-01-28T23:59:59.000Z

238

Hydrous pyrolysis/oxidation process for in situ destruction of chlorinated hydrocarbon and fuel hydrocarbon contaminants in water and soil  

DOE Patents [OSTI]

In situ hydrous pyrolysis/oxidation process is useful for in situ degradation of hydrocarbon water and soil contaminants. Fuel hydrocarbons, chlorinated hydrocarbons, polycyclic aromatic hydrocarbons, petroleum distillates and other organic contaminants present in the soil and water are degraded by the process involving hydrous pyrolysis/oxidation into non-toxic products of the degradation. The process uses heat which is distributed through soils and water, optionally combined with oxygen and/or hydrocarbon degradation catalysts, and is particularly useful for remediation of solvent, fuel or other industrially contaminated sites.

Knauss, Kevin G. (Livermore, CA); Copenhaver, Sally C. (Livermore, CA); Aines, Roger D. (Livermore, CA)

2000-01-01T23:59:59.000Z

239

Evaluation of microporous carbon filters as catalysts for ozone decomposition  

SciTech Connect (OSTI)

Ozone is produced in small quantities in photocopiers and laser printers in the workplace and large quantities in industrial waste water treatment facilities. Carbon filters are commonly used to decompose this unwanted ozone. The three most important factors in producing a filter for this purpose are flow properties, efficiency, and cost. Most ozone decomposition applications require very low back-pressure at modest flow rates. The tradeoff between the number of pores and the size of the pores will be discussed. Typical unfiltered emissions in the workplace are approximately 1 ppm. The maximum permissible exposure limit, PEL, for worker exposure to ozone is 0.1 ppm over 8 hours. Several methods have been examined to increase the efficiency of ozone decomposition. Carbon surfaces were modified with catalysts, the surface activated, and the surface area was increased, in attempts to decompose ozone more effectively. Methods to reduce both the processing and raw material costs were investigated. Several sources of microporous carbon were investigated as ozone decomposition catalysts. Cheaper processing routes including macropore templating, faster drying and extracting methods were also studied.

Whinnery, L.; Coutts, D.; Shen, C.; Adams, R. [Sandia National Labs., Livermore, CA (United States); Quintana, C.; Showalter, S. [Sandia National Labs., Albuquerque, NM (United States)

1994-12-31T23:59:59.000Z

240

Exposure-Relevant Ozone Chemistry in Occupied Spaces  

SciTech Connect (OSTI)

Ozone, an ambient pollutant, is transformed into other airborne pollutants in the indoor environment. In this dissertation, the type and amount of byproducts that result from ozone reactions with common indoor surfaces, surface residues, and vapors were determined, pollutant concentrations were related to occupant exposure, and frameworks were developed to predict byproduct concentrations under various indoor conditions. In Chapter 2, an analysis is presented of secondary organic aerosol formation from the reaction of ozone with gas-phase, terpene-containing consumer products in small chamber experiments under conditions relevant for residential and commercial buildings. The full particle size distribution was continuously monitored, and ultrafine and fine particle concentrations were in the range of 10 to>300 mu g m-3. Particle nucleation and growth dynamics were characterized.Chapter 3 presents an investigation of ozone reactions with aircraft cabin surfaces including carpet, seat fabric, plastics, and laundered and worn clothing fabric. Small chamber experiments were used to determine ozone deposition velocities, ozone reaction probabilities, byproduct emission rates, and byproduct yields for each surface category. The most commonly detected byproducts included C1?C10 saturated aldehydes and skin oil oxidation products. For all materials, emission rates were higher with ozone than without. Experimental results were used to predict byproduct exposure in the cabin and compare to other environments. Byproduct levels are predicted to be similar to ozone levels in the cabin, which have been found to be tens to low hundreds of ppb in the absence of an ozone converter. In Chapter 4, a model is presented that predicts ozone uptake by and byproduct emission from residual chemicals on surfaces. The effects of input parameters (residue surface concentration, ozone concentration, reactivity of the residue and the surface, near-surface airflow conditions, and byproduct yield) were explored. In Chapter 5, the reaction of ozone with permethrin, a residual insecticide used in aircraft cabins, to form phosgene is investigated. A derivatization technique was developed to detect phosgene at low levels, and chamber experiments were conducted with permethrin-coated cabin materials. It was determined that phosgene formation, if it occurs in the aircraft cabin, is not likely to exceed the relevant, health-based phosgene exposure guidelines.

Coleman, Beverly Kaye

2009-04-01T23:59:59.000Z

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" from the National Library of EnergyBeta (NLEBeta).
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241

Ozone generation by rock fracture: Earthquake early warning?  

SciTech Connect (OSTI)

We report the production of up to 10 ppm ozone during crushing and grinding of typical terrestrial crust rocks in air, O{sub 2} and CO{sub 2} at atmospheric pressure, but not in helium or nitrogen. Ozone is formed by exoelectrons emitted by high electric fields, resulting from charge separation during fracture. The results suggest that ground level ozone produced by rock fracture, besides its potential health hazard, can be used for early warning in earthquakes and other catastrophes, such as landslides or land shifts in excavation tunnels and underground mines.

Baragiola, Raul A.; Dukes, Catherine A.; Hedges, Dawn [Engineering Physics, University of Virginia, Charlottesville, Virginia 22904 (United States)

2011-11-14T23:59:59.000Z

242

HYDROCARBON-DEGRADING BACTERIA AND SURFACTANT ACTIVITY  

SciTech Connect (OSTI)

Fate of benzene ethylbenzene toluene xylenes (BTEX) compounds through biodegradation was investigated using two different bacteria, Ralstonia picketti (BP-20) and Alcaligenes piechaudii (CZOR L-1B). These bacteria were isolated from extremely polluted petroleum hydrocarbon contaminated soils. PCR and Fatty Acid Methyl Ester (FAME) were used to identify the isolates. Biodegradation was measured using each organism individually and in combination. Both bacteria were shown to degrade each of the BTEX compounds. Alcaligenes piechaudii biodegraded BTEXs more efficiently while mixed with BP-20 and individually. Biosurfactant production was observed by culture techniques. In addition 3-hydroxy fatty acids, important in biosurfactant production, was observed by FAME analysis. In the all experiments toluene and m+p- xylenes were better growth substrates for both bacteria than the other BTEX compounds. In addition, the test results indicate that the bacteria could contribute to bioremediation of aromatic hydrocarbons (BTEX) pollution increase biodegradation through the action by biosurfactants.

Brigmon, R; Topher Berry, T; Grazyna A. Plaza, G; jacek Wypych, j

2006-08-15T23:59:59.000Z

243

Behavioral toxicology, risk assessment, and chlorinated hydrocarbons  

SciTech Connect (OSTI)

Behavioral end points are being used with greater frequency in neurotoxicology to detect and characterize the adverse effects of chemicals on the nervous system. Behavioral measures are particularly important for neurotoxicity risk assessment since many known neurotoxicants do not result in neuropathology. The chlorinated hydrocarbon class consists of a wide variety of chemicals including polychlorinated biphenyls, clioquinol, trichloroethylene, hexachlorophene, organochlorine insecticides (DDT, dicofol, chlordecone, dieldrin, and lindane), and phenoxyherbicides. Each of these chemicals has effects on motor, sensory, or cognitive function that are detectable using functional measures such as behavior. Furthermore, there is evidence that if exposure occurs during critical periods of development, many of the chlorinated hydrocarbons are developmental neurotoxicants. Developmental neurotoxicity is frequently expressed as alterations in motor function or cognitive abilities or charges in the ontogeny of sensorimotor reflexes. Neurotoxicity risk assessment should include assessments of the full range of possible neurotoxicological effects, including both structural and functional indicators of neurotoxicity. 121 refs., 1 tab.

Evangelista de Duffard, A.M.; Duffard, R. [Laboratorio de Toxicologia Experimental, Santa Fe (Argentina)

1996-04-01T23:59:59.000Z

244

Method and apparatus for synthesizing hydrocarbons  

DOE Patents [OSTI]

A method and apparatus for synthesizing a mixture of hydrocarbons having five carbons or less is disclosed. An equal molar ratio of CO and H/sub 2/ gases is caused to pass through a ThO/sub 2/ catalyst having a surface area of about 80 to 125 m/sup 2//g. The catalyst further includes Na present as a substitutional cation in an amount of about 5 to 10 atom %. At a temperature of about 340 to 360/sup 0/C, and at pressures of about 20 to 50 atm, CH/sub 3/OH is produced in an amount of about 90 wt % of the total hydrocarbon mixture, and comprised 1 mole % of the effluent gas.

Colmenares, C.A.; Somorjai, G.A.; Maj, J.J.

1983-06-21T23:59:59.000Z

245

Monitoring of vapor phase polycyclic aromatic hydrocarbons  

DOE Patents [OSTI]

An apparatus for monitoring vapor phase polycyclic aromatic hydrocarbons in a high-temperature environment has an excitation source producing electromagnetic radiation, an optical path having an optical probe optically communicating the electromagnetic radiation received at a proximal end to a distal end, a spectrometer or polychromator, a detector, and a positioner coupled to the first optical path. The positioner can slidably move the distal end of the optical probe to maintain the distal end position with respect to an area of a material undergoing combustion. The emitted wavelength can be directed to a detector in a single optical probe 180.degree. backscattered configuration, in a dual optical probe 180.degree. backscattered configuration or in a dual optical probe 90.degree. side scattered configuration. The apparatus can be used to monitor an emitted wavelength of energy from a polycyclic aromatic hydrocarbon as it fluoresces in a high temperature environment.

Vo-Dinh, Tuan; Hajaligol, Mohammad R.

2004-06-01T23:59:59.000Z

246

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

247

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

248

Production of synthetic hydrocarbon fuels from peat  

SciTech Connect (OSTI)

A process and apparatus for production of synthetic hydrocarbon fuels from peat providing wide variation of the composite proportion of liquid-gas output while maintaining high overall carbon conversion to useful fuel. The process and apparatus utilizes three process stages in a single vessel providing functions of drying wet peat, provisions for addition of both wet and dry peat to a hydropyrolysis zone and gasification of the peat char.

Bodle, W.W.; Punwani, D.; Weil, S.A.

1982-06-22T23:59:59.000Z

249

Getter pump for hydrogen and hydrocarbon gases  

DOE Patents [OSTI]

A gettering device for hydrogen isotopes and gaseous hydrocarbons based on the interaction of a plasma and graphite used as cathodic material. The plasma is maintained at a current density within the range of about 1 to about 1000 mA/cm/sup 2/. The graphite may be heated to a temperature greater than 1000/degree/C. The new device offers high capacity, low noise, and gas species selectivity. 2 figs.

Hsu, Wen Ling

1987-10-14T23:59:59.000Z

250

Oxidative dehydrogenation of alkanes to unsaturated hydrocarbons  

DOE Patents [OSTI]

Oxidative dehydrogenation of alkanes to unsaturated hydrocarbons is carried out over metal vanadate catalysts under oxidizing conditions. The vanadate catalysts are represented by the formulas M[sub 3](VO[sub 4])[sub 2] and MV[sub 2]O[sub 6], M representing Mg, Zn, Ca, Pb, or Cd. The reaction is carried out in the presence of oxygen, but the formation of oxygenate by-products is suppressed.

Kung, H.H.; Chaar, M.A.

1988-10-11T23:59:59.000Z

251

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

252

Ozone concentrations in El Paso, Texas  

SciTech Connect (OSTI)

El Paso, Texas may have a problem in meeting ambient air standards due to influx of pollutants from foreign sources. Cd. Juarez, Chihuahua, and Fort Bliss abut the city and are areas over which the Texas Air Control Board (TACB) has little or no jurisdiction. The Board maintains two Continuous Air Monitoring Stations (CAM) in El Paso. Ozone, nitric oxide, and nitrogen dioxide data were obtained from these stations. If the EPA Empirical Kinetic Model is used for El Paso, reducing NMHC concentrations may increase rather than decrease O/sub 3/ concentrations. The Texas State Implementation Plan, while not based on Empirical Kinetic Modeling, calls for a reduction of 18% in NMHC. However, 31% of all NMHC in El Paso arise from sources over which Texas had little (a federal military reservation) or no (Cd. Juarez) jurisdiction. It appears the TACB is correct in believing the SIP for O/sub 3/ may not bring El Paso into compliance. (JMT)

Crocker, J.E. (Texas Air Control Board, Austin); Applegate, H.G.

1983-02-01T23:59:59.000Z

253

Phase Behavior of Light Gases in Hydrocarbon and Aqueous Solvents  

SciTech Connect (OSTI)

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

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

1997-09-01T23:59:59.000Z

254

PREFERENTIAL OXIDATION OF CARBON MONOXIDE IN A THIN-FILM CATALYTIC MICROREACTOR: ADVANTAGES AND LIMITATIONS  

E-Print Network [OSTI]

-PBR's favor the reverse water-gas-shift (r-WGS) reaction, thus causing a much narrower range of permissible stream after hydrocarbon fuel reforming and water-gas-shift reactions. This process, referred to as CO;2 ABSTRACT Silicon microreactors with thin-film wall catalyst were adopted for kinetic studies of CO

Besser, Ronald S.

255

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

256

Attosecond electronic and nuclear quantum photodynamics of the ozone molecule  

SciTech Connect (OSTI)

Coupled electron-nuclear dynamics simulations are investigated for the ozone molecule on the attosecond time scale. The initial wavepacket is pumped as a coherent superposition of two or three electronic states.

Halász, G. J. [Department of Information Technology, University of Debrecen, H-4010 Debrecen, PO Box 12 (Hungary)] [Department of Information Technology, University of Debrecen, H-4010 Debrecen, PO Box 12 (Hungary); Perveaux, A.; Lasorne, B.; Gatti, F. [CTMM, Institut Charles Gerhardt Montpellier, F-34095 Montpellier Cedex 5 (France)] [CTMM, Institut Charles Gerhardt Montpellier, F-34095 Montpellier Cedex 5 (France); Robb, M. A. [Imperial College London, Department of Chemistry, London SW7 2AZ (United Kingdom)] [Imperial College London, Department of Chemistry, London SW7 2AZ (United Kingdom); Vibók, Á. [Department of Theoretical Physics, University of Debrecen, H-40410 Debrecen, PO Box 5 (Hungary)] [Department of Theoretical Physics, University of Debrecen, H-40410 Debrecen, PO Box 5 (Hungary)

2013-11-13T23:59:59.000Z

257

Global Health and Economic Impacts of Future Ozone Pollution  

E-Print Network [OSTI]

We assess the human health and economic impacts of projected 2000-2050 changes in ozone pollution using the MIT Emissions Prediction and Policy Analysis-Health Effects (EPPA-HE) model, in combination with results from the ...

Webster, Mort D.

258

Method for producing hydrocarbon and alcohol mixtures. [Patent application  

DOE Patents [OSTI]

It is an object of this invention to provide an efficient process for extracting alcohols and ketones from an aqueous solution containing the same into hydrocarbon fuel mixtures, such as gasoline, diesel fuel and fuel oil. Another object of the invention is to provide a mixture consisting of hydrocarbon, alcohols or ketones, polyoxyalkylene polymer and water which can be directly added to fuels or further purified. The above stated objects are achieved in accordance with a preferred embodiment of the invention by contacting an aqueous fermentation liquor with a hydrocarbon or hydrocarbon mixture containing carbon compounds having 5 to 18 carbon atoms, which may include gasoline, diesel fuel or fuel oil. The hydrocarbon-aqueous alcohol solution is mixed in the presence or one or more of a group of polyoxyalkylene polymers described in detail hereinafter; the fermentation alcohol being extracted into the hydrocarbon fuel-polyoxyalkylene polymer mixture.

Compere, A.L.; Googin, J.M.; Griffith, W.L.

1980-12-01T23:59:59.000Z

259

The role of ozone in tracheal cell transformation  

SciTech Connect (OSTI)

This project examined the potential role of ozone as a respiratory carcinogen by characterizing its ability to induce or modulate the preneoplastic transformation of rat tracheal epithelial cells. The chemical reactivity of ozone and the types of damage it can cause suggest that it may have a role in environmental carcinogenesis. Few other studies have examined the direct cytotoxic or transforming effects of ozone after in vivo or in vitro exposure of cells, and no studies have been reported on the comparative effects of ozone on respiratory cells exposed in vivo or in vitro. The induction of early preneoplastic changes in populations of rat tracheal epithelial cells by carcinogens can be detected and quantified in vitro after exposures in vivo or in vitro of tracheal epithelial cells. This cell culture and transformation system was used to characterize the transforming potency of ozone. Tracheal epithelial cells were isolated from Fischer-344/N rats that had been exposed for six hours per day, five days per week for one, two, or four weeks to 0, 0.12, 0.5, or 1.0 parts per million (ppm)* ozone (sea-level equivalents). Cell populations were examined in culture for increases in the frequency of preneoplastic variants. Rats exposed to ozone did not exhibit an increase in the frequency of preneoplastic tracheal cells, although exposed tracheas did exhibit dose-dependent morphological changes. Rat tracheal epithelial cells were given single, 40-minute in vitro exposures to concentrations of ozone that did not result in any detectable decrease in colony-forming efficiency.

Thomassen, D.G.; Harkema, J.R.; Sun, J.D.; Stephens, N.D.; Griffith, W.C. (Inhalation Toxicology Research Institute, Lovelace Biomedical and Environmental Research Institute, Albuquerque, NM (United States))

1992-04-01T23:59:59.000Z

260

An experimental and mathematical investigation of hydrocarbon steam distillation  

E-Print Network [OSTI]

of Committee) Dr. Pau B. Crawford (Member) r. William D. McCain Jr. r. A ber t T. Watson (Member) Dr. i l. iam D. on Gonten ead of Department) December 1984 ABSTRACT An Experimental and Mathematical Investigation of Hydrocarbon Steam Distillation... mechanism associated with steam flooding and in-situ combustion enhanced oil recovery projects. It also takes place in hydrocarbon recovery from deep volatile oil reservoirs. Nethods for predicting the recovery of hydrocarbons by steam distillation have...

Langhoff, John Allan

1984-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

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

262

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.

263

Commercialization of IH2® Biomass Direct-to-Hydrocarbon Fuel...  

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

Commercialization of IH 2 Biomass Direct-to-Hydrocarbon Fuel Technology Alan Del Paggio, Vice President CRI Catalyst Company 910 Louisiana, Houston, TX 77002 Disclaimer This...

264

Biological Conversion of Sugars to Hydrocarbons Technology Pathway...  

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

case investigates the biological conversion of biomass-derived sugars to hydrocarbon biofuels, utilizing data from recent literature references and information consistent with...

265

Systems and methods for producing hydrocarbons from tar sands formations  

DOE Patents [OSTI]

A system for treating a tar sands formation is disclosed. A plurality of heaters are located in the formation. The heaters include at least partially horizontal heating sections at least partially in a hydrocarbon layer of the formation. The heating sections are at least partially arranged in a pattern in the hydrocarbon layer. The heaters are configured to provide heat to the hydrocarbon layer. The provided heat creates a plurality of drainage paths for mobilized fluids. At least two of the drainage paths converge. A production well is located to collect and produce mobilized fluids from at least one of the converged drainage paths in the hydrocarbon layer.

Li, Ruijian (Katy, TX); Karanikas, John Michael (Houston, TX)

2009-07-21T23:59:59.000Z

266

Process for making unsaturated hydrocarbons using microchannel process technology  

DOE Patents [OSTI]

The disclosed invention relates to a process for converting a feed composition comprising one or more hydrocarbons to a product comprising one or more unsaturated hydrocarbons, the process comprising: flowing the feed composition and steam in contact with each other in a microchannel reactor at a temperature in the range from about 200.degree. C. to about 1200.degree. C. to convert the feed composition to the product, the process being characterized by the absence of catalyst for converting the one or more hydrocarbons to one or more unsaturated hydrocarbons. Hydrogen and/or oxygen may be combined with the feed composition and steam.

Tonkovich, Anna Lee (Dublin, OH); Yuschak, Thomas (Lewis Center, OH); LaPlante, Timothy J. (Columbus, OH); Rankin, Scott (Columbus, OH); Perry, Steven T. (Galloway, OH); Fitzgerald, Sean Patrick (Columbus, OH); Simmons, Wayne W. (Dublin, OH); Mazanec, Terry (Solon, OH) Daymo, Eric (Dublin, OH)

2011-04-12T23:59:59.000Z

267

Biological Production of a Hydrocarbon Fuel IntermediatePolyhydroxybu...  

Office of Scientific and Technical Information (OSTI)

Biological Production of a Hydrocarbon Fuel Intermediate Polyhydroxybutyrate (PHB) from a Process Relevant Lignocellulosic Derived Sugar (Poster) Re-direct Destination: PHAs are...

268

Selective aerobic oxidation of hydrocarbons over supported gold catalysts.  

E-Print Network [OSTI]

??The selective oxidation of hydrocarbons is of vital importance for the production of valuable chemicals from crude oil and natural gas resources. Unfortunately, when using… (more)

Hereijgers, B.P.C.

2011-01-01T23:59:59.000Z

269

Algal Lipid Extraction and Upgrading to Hydrocarbons Technology...  

Energy Savers [EERE]

of algal biomass followed by further lipid extraction and upgrading to hydrocarbon biofuels. Technical barriers and key research needs have been assessed in order for the algal...

270

Catalytic Upgrading of Sugars to Hydrocarbons Technology Pathway...  

Energy Savers [EERE]

the catalytic conversion of solubilized carbohydrate streams to hydrocarbon biofuels, utilizing data from recent efforts within the National Advanced Biofuels Consortium...

271

Catalytic Upgrading of Sugars to Hydrocarbons Technology Pathway  

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

Fractionation Hydrogen Acid, Caustic, Enzymes Wastewater Treatment Insoluble solids Biogas + Sludge Process Heat and Power Integration Corn Stover Hydrocarbon Biofuels (i.e....

272

Carbonaceous adsorbent regeneration and halocarbon displacement by hydrocarbon gases  

DOE Patents [OSTI]

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

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

1994-01-01T23:59:59.000Z

273

Carbonaceous adsorbent regeneration and halocarbon displacement by hydrocarbon gases  

DOE Patents [OSTI]

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

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

1994-04-05T23:59:59.000Z

274

aromatic hydrocarbon carcinogenesis: Topics by E-print Network  

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

and Ecology Websites Summary: ), and there are oil refineries on the shore. In this environment, input of aromatic hydrocarbons from petroleum and the Yarra River Estuary J. David...

275

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

276

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

277

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

278

Gulf Hydrocarbon Inc | Open Energy Information  

Open Energy Info (EERE)

AFDC Printable Version Share this resource Send a link to EERE: Alternative Fuels Data Center Home Page to someone by E-mail Share EERE: Alternative Fuels Data Center Home Page on Facebook Tweet about EERE: Alternative Fuels Data Center Home Page on Twitter Bookmark EERE: Alternative Fuels Data Center Home Page on Google Bookmark EERE: Alternative Fuels Data Center Home5b9fcbce19 No revision hasInformation Earth's Heat Jump to:Photon Place:Net Jump Agency/Company(Redirected fromHydrocarbon

279

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

280

Proceedings of Healthy Buildings 2009 Paper 141 Removal of Indoor Ozone with Reactive Materials: Preliminary Results and  

E-Print Network [OSTI]

Proceedings of Healthy Buildings 2009 Paper 141 Removal of Indoor Ozone with Reactive Materials air quality. #12;Proceedings of Healthy Buildings 2009 Paper 141 Removing ozone from indoor

Siegel, Jeffrey

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

Preliminary Geospatial Analysis of Arctic Ocean Hydrocarbon Resources  

SciTech Connect (OSTI)

Ice coverage of the Arctic Ocean is predicted to become thinner and to cover less area with time. The combination of more ice-free waters for exploration and navigation, along with increasing demand for hydrocarbons and improvements in technologies for the discovery and exploitation of new hydrocarbon resources have focused attention on the hydrocarbon potential of the Arctic Basin and its margins. The purpose of this document is to 1) summarize results of a review of published hydrocarbon resources in the Arctic, including both conventional oil and gas and methane hydrates and 2) develop a set of digital maps of the hydrocarbon potential of the Arctic Ocean. These maps can be combined with predictions of ice-free areas to enable estimates of the likely regions and sequence of hydrocarbon production development in the Arctic. In this report, conventional oil and gas resources are explicitly linked with potential gas hydrate resources. This has not been attempted previously and is particularly powerful as the likelihood of gas production from marine gas hydrates increases. Available or planned infrastructure, such as pipelines, combined with the geospatial distribution of hydrocarbons is a very strong determinant of the temporal-spatial development of Arctic hydrocarbon resources. Significant unknowns decrease the certainty of predictions for development of hydrocarbon resources. These include: 1) Areas in the Russian Arctic that are poorly mapped, 2) Disputed ownership: primarily the Lomonosov Ridge, 3) Lack of detailed information on gas hydrate distribution, and 4) Technical risk associated with the ability to extract methane gas from gas hydrates. Logistics may control areas of exploration more than hydrocarbon potential. Accessibility, established ownership, and leasing of exploration blocks may trump quality of source rock, reservoir, and size of target. With this in mind, the main areas that are likely to be explored first are the Bering Strait and Chukchi Sea, in spite of the fact that these areas do not have highest potential for future hydrocarbon reserves. Opportunities for improving the mapping and assessment of Arctic hydrocarbon resources include: 1) Refining hydrocarbon potential on a basin-by-basin basis, 2) Developing more realistic and detailed distribution of gas hydrate, and 3) Assessing the likely future scenarios for development of infrastructure and their interaction with hydrocarbon potential. It would also be useful to develop a more sophisticated approach to merging conventional and gas hydrate resource potential that considers the technical uncertainty associated with exploitation of gas hydrate resources. Taken together, additional work in these areas could significantly improve our understanding of the exploitation of Arctic hydrocarbons as ice-free areas increase in the future.

Long, Philip E.; Wurstner, Signe K.; Sullivan, E. C.; Schaef, Herbert T.; Bradley, Donald J.

2008-10-01T23:59:59.000Z

282

Process for the production of liquid hydrocarbons  

DOE Patents [OSTI]

The present invention concerns a process for the preparation of liquid hydrocarbons which process comprises contacting synthesis gas with a slurry of solid catalyst particles and a liquid in a reactor vessel by introducing the synthesis gas at a low level into the slurry at conditions suitable for conversion of the synthesis gas into liquid hydrocarbons, the solid catalyst particles comprising a catalytic active metal selected from cobalt or iron on a porous refractory oxide carrier, preferably selected from silica, alumina, titania, zirconia or mixtures thereof, the catalyst being present in an amount between 10 and 40 vol. percent based on total slurry volume liquids and solids, and separating liquid material from the solid catalyst particles by using a filtration system comprising an asymmetric filtration medium (the selective side at the slurry side), in which filtration system the average pressure differential over the filtration medium is at least 0.1 bar, in which process the particle size distribution is such that at least a certain amount of the catalyst particles is smaller than the average pore size of the selective layer of the filtration medium. The invention also comprises an apparatus to carry out the process described above.

Bhatt, Bharat Lajjaram; Engel, Dirk Coenraad; Heydorn, Edward Clyde; Senden, Matthijis Maria

2006-06-27T23:59:59.000Z

283

Solubility of hydrocarbons in salt water  

SciTech Connect (OSTI)

In the design and operation of industrial processes, physical and thermodynamic property data are required. Increasingly stringent regulations are making water solubility of substances even more critical. Water solubility data of naphthenes, or cycloalkanes, is applicable for the complete range of salt concentrations, including water without salt to water saturated with salt. The results are intended for use in initial engineering and environmental applications. Solubility values from the correlation are useful in determining the distribution of a hydrocarbon spill on its contact with sea water. Solubility values at other salt concentrations also may be computed. Results are presented for water solubility of hydrocarbons (naphthenes) as a function of salt concentration (log(S) = A + BX + CX[sup 2]). The correlation constants, A, B and C, are displayed in an easy-to-use tabular format that is applicable for rapid engineering use with the personal computer or hand-held calculator. The results for solubility in salt water are applicable for the complete range of salt concentrations. This range covers water without salt, X = 0, to water saturated with salt, X = 358,700 ppM(wt). Correlation and experimental results are in favorable agreement.

Yaws, C.L.; Lin, X. (Lamar Univ., Beaumont, TX (United States). Dept. of Chemical Engineering)

1994-01-01T23:59:59.000Z

284

Scroll compressor modelling for heat pumps using hydrocarbons as refrigerants  

E-Print Network [OSTI]

1 Scroll compressor modelling for heat pumps using hydrocarbons as refrigerants Paul BYRNE and to install heat pumps in unoccupied spaces. Nevertheless manufacturers keep working on components for hydrocarbons. In the frame of a research project on heat pumps for simultaneous heating and cooling, an R407C

Paris-Sud XI, Université de

285

Biological Conversion of Sugars to Hydrocarbons Technology Pathway  

SciTech Connect (OSTI)

This technology pathway case investigates the biological conversion of biomass-derived sugars to hydrocarbon biofuels, utilizing data from recent literature references and information consistent with recent pilot-scale demonstrations at NREL. Technical barriers and key research needs have been identified that should be pursued for the pathway to become competitive with petroleum-derived gasoline-, diesel-, and jet-range hydrocarbon blendstocks.

Davis, R.; Biddy, M.; Tan, E.; Tao, L.; Jones, S.

2013-03-01T23:59:59.000Z

286

.. Polycyclic aromatic hydrocarbons in nearshore marine sediments of Australia*  

E-Print Network [OSTI]

143 . .. Polycyclic aromatic hydrocarbons in nearshore marine sediments of Australia* W.A. Maher and J. Aislabiet Water Research Centre, University of Canberra, PO Box /, Belconnen,ACT 26/6, Australia aromatic hydrocarbons (PAH) in nearshore marine sediments of Australia isdiscussed. Available information

Canberra, University of

287

Selective thermal and photooxidation of hydrocarbons in zeolites by oxygen  

DOE Patents [OSTI]

A process is described for selective thermal oxidation or photooxidation of hydrocarbons adsorbed onto zeolite matrices. A highly selective thermal oxidation and photooxidation of unsubstituted or alkyl substituted alkanes, alkenes, aromatics and cycloalkyls in solvent free zeolites under dark thermal conditions or under irradiation with visible light. The process oxidizes hydrocarbons almost completely selectively without substantial production of byproducts. 19 figs.

Frei, H.; Blatter, F.; Sun, H.

1999-06-22T23:59:59.000Z

288

Selective thermal and photooxidation of hydrocarbons in zeolites by oxygen  

DOE Patents [OSTI]

A process for selective thermal oxidation or photooxidation of hydrocarbons adsorbed onto zeolite matrices. A highly selective thermal oxidation and photooxidation of unsubstituted or alkyl substituted alkanes, alkenes, aromatics and cycloalkyls in solvent free zeolites under dark thermal conditions or under irradiation with visible light. The process oxidizes hydrocarbons almost completely selectively without substantial production of byproducts.

Frei, Heinz (Berkeley, CA); Blatter, Fritz (Basel, CH); Sun, Hai (Saint Charles, MO)

1999-01-01T23:59:59.000Z

289

Selective thermal oxidation of hydrocarbons in zeolites by oxygen  

DOE Patents [OSTI]

A process for selective thermal oxidation of hydrocarbons adsorbed onto zeolite matrices. A highly selective thermal oxidation of unsubstituted or alkyl substituted alkanes, alkenes, aromatics and cycloalkyls is carried out in solvent free zeolites under dark thermal conditions. The process oxidizes hydrocarbons almost completely selectively without substantial production of byproducts.

Frei, Heinz (Berkeley, CA); Blatter, Fritz (Basel, CH); Sun, Hai (Saint Charles, MO)

2000-01-01T23:59:59.000Z

290

Selective thermal and photooxidation of hydrocarbons in zeolites by oxygen  

DOE Patents [OSTI]

A process for a combined selective thermal oxidation and photooxidation of hydrocarbons adsorbed onto zeolite matrices. A highly combined selective thermal oxidation and photooxidation of unsubstituted or alkyl substituted alkanes, alkenes, aromatics and cycloalkyls in solvent free zeolites under dark thermal conditions or under irradiation with visible light. The process oxidizes hydrocarbons almost completely selectively without substantial production of byproducts.

Frei, Heinz (Berkeley, CA); Blatter, Fritz (Basel, CH); Sun, Hai (Saint Charles, MO)

2001-01-01T23:59:59.000Z

291

Comparison of three vertically resolved ozone data sets: climatology, trends and radiative forcings  

E-Print Network [OSTI]

Climate models that do not simulate changes in stratospheric ozone concentrations require the prescription of ozone fields to accurately calculate UV fluxes and stratospheric heating rates. In this study, three different ...

Hassler, B.

292

Atmospheric Environment 38 (2004) 14251436 A development of ozone abatement strategies for the Grenoble  

E-Print Network [OSTI]

Atmospheric Environment 38 (2004) 1425­1436 A development of ozone abatement strategies are generated in the Grenoble plume. For developing ozone abatement strategies it is important to know whether

293

A delayed effect of ozone fumigation on photosynthesis of Norway spruce  

E-Print Network [OSTI]

A delayed effect of ozone fumigation on photosynthesis of Norway spruce D. Eamus1 A.W. Davis J into the long-lastincl effects of ozone fumiga- tion upon photosynthesis of Norway spruce. Measurements were

Paris-Sud XI, Université de

294

E-Print Network 3.0 - acute ozone-induced change Sample Search...  

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

Abstract Predicting ozone-induced reduction of carbon... a leaf-level model to the whole tree, it is possible to investigate whether the ozone-induced ... Source: Michigan...

295

Examination of the Effects of Sea Salt Aerosols on Southeast Texas Ozone and Secondary Organic Aerosol  

E-Print Network [OSTI]

such as ozone, reactive nitrogen, mercury, and sulfur containing compounds. Urban areas are most impacted by these trace gases, which is a concern because ozone especially affects the health of citizens. Experiments have three basic parts. First we generate mono...

Benoit, Mark David

2013-02-06T23:59:59.000Z

296

Pilot Scale Study of Excess Sludge Production Reduction in Wastewater Treatment by Ozone  

E-Print Network [OSTI]

Pilot Scale Study of Excess Sludge Production Reduction in Wastewater Treatment by Ozone Yuan Ma-scale reactors were operated at the LaPrairie Wastewater Treatment plant (one control and one ozonated

Barthelat, Francois

297

E-Print Network 3.0 - acid regulates ozone-induced Sample Search...  

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

ozone-induced Search Powered by Explorit Topic List Advanced Search Sample search results for: acid regulates ozone-induced Page: << < 1 2 3 4 5 > >> 1 Plant Molecular Biology 51:...

298

E-Print Network 3.0 - aromatic hydrocarbon exposure Sample Search...  

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

Aust. J. Mar. Freshw. Res., 1984, 35, 119-28 Aromatic Hydrocarbons in Waters of Port Phillip Bay... of aromatic hydrocarbons in coastal waters, using solvent extraction and...

299

E-Print Network 3.0 - aromatic hydrocarbons influence Sample...  

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

; Geosciences 93 Hydrocarbons Heterogeneous Pyrolysis: Experiments and Modeling for Scramjet Thermal Management Summary: of the decomposition of the heavy hydrocarbon fuel is the...

300

E-Print Network 3.0 - aromatic hydrocarbon unresolved Sample...  

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

40 On the Use, and Reuse, of Polymers for the Treatment of Hydrocarbon Contaminated Water Via a Solidliquid Partitioning Bioreactor Summary: hydrocarbons and more heavily...

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

E-Print Network 3.0 - aromatic hydrocarbons alcohols Sample Search...  

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

Mathematics 29 UV Irradiation of Polycyclic Aromatic Hydrocarbons in Ices Summary: UV Irradiation of Polycyclic Aromatic Hydrocarbons in Ices: Production of Alcohols,...

302

E-Print Network 3.0 - aromatic hydrocarbons exhibited Sample...  

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

of Port Phillip Bay... of aromatic hydrocarbons in coastal waters, using solvent extraction and fluorescence emission analysis, shows... of hydrocarbon inputs....

303

E-Print Network 3.0 - aromatic hydrocarbons molecules Sample...  

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

Sciences and Ecology 35 2006-01-0201 Speciated Hydrocarbon Emissions from an Automotive Diesel Summary: to number of carbon atoms per hydrocarbon molecule (Figure 2). For each...

304

E-Print Network 3.0 - aromatic hydrocarbons resulting Sample...  

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

Geosciences 50 2006-01-0201 Speciated Hydrocarbon Emissions from an Automotive Diesel Summary: a retention library developed by performing runs with known hydrocarbon...

305

E-Print Network 3.0 - aromatic hydrocarbons determined Sample...  

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

Mathematics 39 2006-01-0201 Speciated Hydrocarbon Emissions from an Automotive Diesel Summary: hydrocarbons is by their structure. Figure 10 shows conversion efficiency...

306

E-Print Network 3.0 - aromatic hydrocarbons formed Sample Search...  

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

Sciences and Ecology 31 2006-01-0201 Speciated Hydrocarbon Emissions from an Automotive Diesel Summary: of engine-out hydrocarbons that are partially reacted fuel. LATE FORMING...

307

E-Print Network 3.0 - aromatic hydrocarbon content Sample Search...  

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

Technologies 23 2006-01-0201 Speciated Hydrocarbon Emissions from an Automotive Diesel Summary: hydrocarbons is by their structure. Figure 10 shows conversion efficiency...

308

E-Print Network 3.0 - aromatic hydrocarbon molecules Sample Search...  

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

Sciences and Ecology 35 2006-01-0201 Speciated Hydrocarbon Emissions from an Automotive Diesel Summary: to number of carbon atoms per hydrocarbon molecule (Figure 2). For each...

309

E-Print Network 3.0 - aromatic hydrocarbon contamination Sample...  

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

Summary: called aromatic hydrocarbons. These include harmful pollutants like dioxins, PCBs and a group called... polycyclic aromatic hydrocarbons (PAHs). PAHs are...

310

E-Print Network 3.0 - aromatic hydrocarbon receptor Sample Search...  

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

aromatic hydrocarbons... the aryl hydrocarbon receptor (AHR), through which dioxins and dioxin-like compounds cause altered gene... -methylcholanthrene AHH: aryl...

311

E-Print Network 3.0 - aromatic hydrocarbons extracted Sample...  

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

of Toxic Contamination Summary: called aromatic hydrocarbons. These include harmful pollutants like dioxins, PCBs and a group called... polycyclic aromatic hydrocarbons (PAHs)....

312

E-Print Network 3.0 - aromatic hydrocarbon metabolism Sample...  

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

hydrocarbon is introduced into the ocean via oil spillage, offshore drilling leaks, industrial... hydrocarbons have been attributed to inhibition of ... Source: National...

313

The Impact of Low Octane Hydrocarbon Blending Streams on "E85...  

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

The Impact of Low Octane Hydrocarbon Blending Streams on "E85" Engine Optimization The Impact of Low Octane Hydrocarbon Blending Streams on "E85" Engine Optimization...

314

E-Print Network 3.0 - aromatic hydrocarbon-degrading bacteria...  

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

ydrocarbonDegradation It was hypothesized... aromatic hydrocarbon degradation. Hypothesis Test Result Groundwater stimulates Fe(lll) reduction Cell... Hydrocarbon Degradation At...

315

Heating hydrocarbon containing formations in a line drive staged process  

DOE Patents [OSTI]

Method for treating a hydrocarbon containing formation are described herein. Methods may include providing heat to a first section of the formation with one or more first heaters in the first section. First hydrocarbons may be heated in the first section such that at least some of the first hydrocarbons are mobilized. At least some of the mobilized first hydrocarbons may be produced through a production well located in a second section of the formation. The second section may be located substantially adjacent to the first section. A portion of the second section may be provided some heat from the mobilized first hydrocarbons, but is not conductively heated by heat from the first heaters. Heat may be provided to the second section with one or more second heaters in the second section to further heat the second section.

Miller, David Scott (Katy, TX)

2009-07-21T23:59:59.000Z

316

Cogeneration systems and processes for treating hydrocarbon containing formations  

DOE Patents [OSTI]

A system for treating a hydrocarbon containing formation includes a steam and electricity cogeneration facility. At least one injection well is located in a first portion of the formation. The injection well provides steam from the steam and electricity cogeneration facility to the first portion of the formation. At least one production well is located in the first portion of the formation. The production well in the first portion produces first hydrocarbons. At least one electrical heater is located in a second portion of the formation. At least one of the electrical heaters is powered by electricity from the steam and electricity cogeneration facility. At least one production well is located in the second portion of the formation. The production well in the second portion produces second hydrocarbons. The steam and electricity cogeneration facility uses the first hydrocarbons and/or the second hydrocarbons to generate electricity.

Vinegar, Harold J. (Bellaire, TX); Fowler, Thomas David (Houston, TX); Karanikas, John Michael (Houston, TX)

2009-12-29T23:59:59.000Z

317

A generalized viscosity equation for pure heavy hydrocarbons  

SciTech Connect (OSTI)

This paper presents a method for the correlation and prediction of the viscosity of pure heavy hydrocarbons listed in API Research Project 42. The 273 heavy hydrocarbons in the database include branched/unbranched paraffins and olefins together with a variety of complex nonfused/fused aromatic and naphthenic compounds. A generalized one-parameter viscosity-temperature equation, log ({mu} + 0.8) = 100(0.01T){sup b}, is proposed (overall AAD {lt} 7-10%) for all heavy hydrocarbons in the database. For each hydrocarbon, an optimum value of parameter b is provided. It is shown that parameter b varies linearly with the logarithm of molar mass as well as the inverse of boiling temperature (at 10 mmHg). This important observation leads to the development of a predictive method for the liquid-phase viscosity of pure heavy hydrocarbons.

Mehrotra, A.K. (Dept. of Chemical and Petroleum Engineering, Univ. of Calgary, Calgary, Alberta T2N 1N4 (CA))

1991-02-01T23:59:59.000Z

318

Meteorological Simulations of Ozone Episode Case Days during the 1996 Paso del Norte Ozone Study  

SciTech Connect (OSTI)

Meteorological simulations centered around the border cities of El Paso and Ciudad Juarez have been performed during an ozone episode that occurred on Aug. 13,1996 during the 1996 Paso del Norte Ozone Study field campaign. Simulations were petiormed using the HOTMAC mesoscale meteorological model using a 1,2,4, and 8 km horizontal grid size nested mesh system. Investigation of the vertical structure and evolution of the atmospheric boundary layer for the Aug. 11-13 time period is emphasized in this paper. Comparison of model-produced wind speed profiles to rawirisonde and radar profiler measurements shows reasonable agreement. A persistent upper-level jet was captured in the model simulations through data assimilation. In the evening hours, the model was not able to produce the strong wind direction shear seen in the radar wind profiles. Based on virtual potential temperature profile comparisons, the model appears to correctly simulate the daytime growth of the convective mixed layer. However, the model underestimates the cooling of the surface layer at night. We found that the upper-level jet significantly impacted the turbulence structure of the boundary layer, leading to relatively high turbulent kinetic energy (tke) values aloft at night. The model indicates that these high tke values aloft enhance the mid-morning growth of the boundary layer. No upper-level turbulence measurements were available to verify this finding, however. Radar profiler-derived mixing heights do indicate relatively rapid morning growth of the mixed layer.

Brown, M.J.; Costigan, K.; Muller, C.; Wang, G.

1999-02-01T23:59:59.000Z

319

1 Ozone pollution forecasting 3 Herve Cardot, Christophe Crambes and Pascal Sarda.  

E-Print Network [OSTI]

Contents 1 Ozone pollution forecasting 3 Herv´e Cardot, Christophe Crambes and Pascal Sarda. 1;1 Ozone pollution forecasting using conditional mean and conditional quantiles with functional covariates Herv´e Cardot, Christophe Crambes and Pascal Sarda. 1.1 Introduction Prediction of Ozone pollution

Crambes, Christophe

320

Thirdhand Tobacco Smoke: Emerging Evidence and Arguments for a Multidisciplinary Research Agenda  

E-Print Network [OSTI]

include ammonia, acrolein, carbon monoxide, formaldehyde,aldehydes (formaldehyde, acrolein), aromatic hydrocarbons (

Matt, Georg E.

2013-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

Pyrochlore catalysts for hydrocarbon fuel reforming  

DOE Patents [OSTI]

A method of catalytically reforming a reactant gas mixture using a pyrochlore catalyst material comprised of one or more pyrochlores having the composition A2B2-y-zB'yB"zO7-.DELTA., where y>0 and z.gtoreq.0. Distribution of catalytically active metals throughout the structure at the B site creates an active and well dispersed metal locked into place in the crystal structure. This greatly reduces the metal sintering that typically occurs on supported catalysts used in reforming reactions, and reduces deactivation by sulfur and carbon. Further, oxygen mobility may also be enhanced by elemental exchange of promoters at sites in the pyrochlore. The pyrochlore catalyst material may be utilized in catalytic reforming reactions for the conversion of hydrocarbon fuels into synthesis gas (H2+CO) for fuel cells, among other uses.

Berry, David A.; Shekhawat, Dushyant; Haynes, Daniel; Smith, Mark; Spivey, James J.

2012-08-14T23:59:59.000Z

322

Microbial hydrocarbons: back to the future  

SciTech Connect (OSTI)

The defining challenge of energy research in the 21st century is the development and deployment of technologies for large-scale reconfiguration of global energy infrastructure. Modern society is built upon a concentrated yet finite reservoir of diverse hydrocarbons formed through the photosynthetic transformation of several hundred million years of solar energy. In human history, the fossil energy era will be short lived and never repeated. Although the timing of peak oil is extensively debated, it is an eventuality. It is, therefore, imperative that projections for both when it will occur and the degree to which supply will fall short of demand be taken into serious consideration, especially in the sectors of energy technology development, political and economic decision making, and societal energy usage. The requirement for renewable energy systems is no longer a point for discussion, and swift advances on many fronts are vital to counteract current and impending crises in both energy and the environment.

Work, Victoria H.; Beliaev, Alex S.; Konopka, Allan; Posewitz, Matthew C.

2012-03-01T23:59:59.000Z

323

Method and apparatus for synthesizing hydrocarbons  

DOE Patents [OSTI]

A method and apparatus for synthesizing a mixture of aliphatic alcohols having five carbons or less is disclosed. An equal molar ratio of CO and H/sub 2/ gases is caused to pass through a ThO/sub 2/ catalyst having a surface area of about 80 to 125 m/sup 2//g. The catalyst further optionally includes Na ions present as substitutional cations in an amount of about 5 to 10 atom %. At a temperature of about 570 to 630/sup 0/K, and at pressures of about 20 to 50 atm, methanol and isobutanol are the predominant products and are produced in amounts of about 90 wt % of the total hydrocarbon mixture. 6 figs.

Colmenares, C.A.; Somorjai, G.A.; Maj, J.J.

1985-04-16T23:59:59.000Z

324

Geology and hydrocarbon prospects of Latvia  

SciTech Connect (OSTI)

Oil prospects in Latvia are associated with the Baltic syneclise. Latvia occupies about one fourth of that large tectonic depression; zones of oil accumulation continue there from adjacent areas: the Telshai rampart (Lithuania) and the Leba nose (Polish offshore). The oil prospects in separate areas are determined by their position regarding the sources of oil generation--the Gdansk-Kura and Liepaya depressions. The most prospective areas are the Liepaya-Saldus zone of highs and the Pape-Barta trough. The Liepaya-Saldus zone was situated so that the hydrocarbon migration path crossed it. It probably is an important oil accumulation zone. The paper describes the geology of Latvia and the one oil field in Latvia.

Freimanis, A. (Latvian Dept. of Geology, Riga (Latvia)); Margulis, L.; Brangulis, A.; Kanev, S.; Pomerantseva, R. (Inst. of Marine Geology and Geophysics, Riga (Latvia))

1993-12-06T23:59:59.000Z

325

Ozone induces glucose intolerance and systemic metabolic effects in young and aged brown Norway rats  

SciTech Connect (OSTI)

Air pollutants have been associated with increased diabetes in humans. We hypothesized that ozone would impair glucose homeostasis by altering insulin signaling and/or endoplasmic reticular (ER) stress in young and aged rats. One, 4, 12, and 24 month old Brown Norway (BN) rats were exposed to air or ozone, 0.25 or 1.0 ppm, 6 h/day for 2 days (acute) or 2 d/week for 13 weeks (subchronic). Additionally, 4 month old rats were exposed to air or 1.0 ppm ozone, 6 h/day for 1 or 2 days (time-course). Glucose tolerance tests (GTT) were performed immediately after exposure. Serum and tissue biomarkers were analyzed 18 h after final ozone for acute and subchronic studies, and immediately after each day of exposure in the time-course study. Age-related glucose intolerance and increases in metabolic biomarkers were apparent at baseline. Acute ozone caused hyperglycemia and glucose intolerance in rats of all ages. Ozone-induced glucose intolerance was reduced in rats exposed for 13 weeks. Acute, but not subchronic ozone increased ?{sub 2}-macroglobulin, adiponectin and osteopontin. Time-course analysis indicated glucose intolerance at days 1 and 2 (2 > 1), and a recovery 18 h post ozone. Leptin increased day 1 and epinephrine at all times after ozone. Ozone tended to decrease phosphorylated insulin receptor substrate-1 in liver and adipose tissues. ER stress appeared to be the consequence of ozone induced acute metabolic impairment since transcriptional markers of ER stress increased only after 2 days of ozone. In conclusion, acute ozone exposure induces marked systemic metabolic impairments in BN rats of all ages, likely through sympathetic stimulation. - Highlights: • Air pollutants have been associated with increased diabetes in humans. • Acute ozone exposure produces profound metabolic alterations in rats. • Age influences metabolic risk factors in aging BN rats. • Acute metabolic effects are reversible and repeated exposure reduces these effects. • Ozone metabolic effects are only slightly exacerbated in geriatric rats.

Bass, V. [Environmental Public Health Division, National Health and Environmental Effects Research Laboratory, U.S. Environmental Protection Agency, Research Triangle Park, NC (United States); Gordon, C.J.; Jarema, K.A.; MacPhail, R.C. [Toxicity Assessment Division, National Health and Environmental Effects Research Laboratory, U.S. Environmental Protection Agency, Research Triangle Park, NC (United States); Cascio, W.E. [Environmental Public Health Division, National Health and Environmental Effects Research Laboratory, U.S. Environmental Protection Agency, Research Triangle Park, NC (United States); Phillips, P.M. [Toxicity Assessment Division, National Health and Environmental Effects Research Laboratory, U.S. Environmental Protection Agency, Research Triangle Park, NC (United States); Ledbetter, A.D.; Schladweiler, M.C. [Environmental Public Health Division, National Health and Environmental Effects Research Laboratory, U.S. Environmental Protection Agency, Research Triangle Park, NC (United States); Andrews, D. [Research Cores Unit, National Health and Environmental Effects Research Laboratory, U.S. Environmental Protection Agency, Research Triangle Park, NC (United States); Miller, D. [Curriculum in Toxicology, University of North Carolina, Chapel Hill, NC (United States); Doerfler, D.L. [Research Cores Unit, National Health and Environmental Effects Research Laboratory, U.S. Environmental Protection Agency, Research Triangle Park, NC (United States); Kodavanti, U.P., E-mail: kodavanti.urmila@epa.gov [Environmental Public Health Division, National Health and Environmental Effects Research Laboratory, U.S. Environmental Protection Agency, Research Triangle Park, NC (United States)

2013-12-15T23:59:59.000Z

326

Hydrocarbon provinces and productive trends in Libya and adjacent areas  

SciTech Connect (OSTI)

According to the age of major reservoirs, hydrocarbon occurrences in Libya and adjacent areas can be grouped into six major systems which, according to their geographic locations, can be classified into two major hydrocarbon provinces: (1) Sirte-Pelagian basins province, with major reservoirs ranging from middle-late Mesozoic to early Tertiary, and (2) Murzog-Ghadames basins province, with major reservoirs ranging from early Paleozoic to early Mesozoic. In the Sirte-Pelagian basins province, hydrocarbons have been trapped in structural highs or in stratigraphic wedge-out against structural highs and in carbonate buildups. Here, hydrocarbon generation is characterized by the combined effect of abundant structural relief and reservoir development in the same hydrocarbon systems of the same age, providing an excellent example of hydrocarbon traps in sedimentary basins that have undergone extensive tensional fracturing in a shallow marine environment. In the Murzog-Ghadames basins province, hydrocarbons have been trapped mainly in structural highs controlled by paleostructural trends as basement arches which acted as focal points for oil migration and accumulation.

Missallati, A.A. (Agip (N.A.M.E.)Ltd., Tripoli (Libya))

1988-08-01T23:59:59.000Z

327

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

328

Gas-phase energies of actinide oxides -- an assessment of neutral and cationic monoxides and dioxides from thorium to curium  

SciTech Connect (OSTI)

An assessment of the gas-phase energetics of neutral and singly and doubly charged cationic actinide monoxides and dioxides of thorium, protactinium, uranium, neptunium, plutonium, americium, and curium is presented. A consistent set of metal-oxygen bond dissociation enthalpies, ionization energies, and enthalpies of formation, including new or revised values, is proposed, mainly based on recent experimental data and on correlations with the electronic energetics of the atoms or cations and with condensed-phase thermochemistry.

Marcalo, Joaquim; Gibson, John K.

2009-08-10T23:59:59.000Z

329

Plasma Chemistry and Plasma Processing, Vol. 23, No. 3, September 2003 ( 2003) Ozone Production in the Negative DC Corona  

E-Print Network [OSTI]

: Corona discharge; corona plasma; plasma reacting flow; ozone; electrostatic precipitator; Damkohler

Chen, Junhong

330

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

331

Direct conversion of light hydrocarbon gases to liquid fuel  

SciTech Connect (OSTI)

Amoco oil Company, has investigated the direct, non-catalytic conversion of light hydrocarbon gases to liquid fuels (particularly methanol) via partial oxidation. The primary hydrocarbon feed used in these studies was natural gas. This report describes work completed in the course of our two-year project. In general we determined that the methanol yields delivered by this system were not high enough to make it economically attractive. Process variables studied included hydrocarbon feed composition, oxygen concentration, temperature and pressure effects, residence time, reactor design, and reactor recycle.

Kaplan, R.D.; Foral, M.J.

1992-05-16T23:59:59.000Z

332

Method for making hydrogen rich gas from hydrocarbon fuel  

DOE Patents [OSTI]

A method of forming a hydrogen rich gas from a source of hydrocarbon fuel in which the hydrocarbon fuel contacts a two-part catalyst comprising a dehydrogenation portion and an oxide-ion conducting portion at a temperature not less than about 400 C for a time sufficient to generate the hydrogen rich gas while maintaining CO content less than about 5 volume percent. There is also disclosed a method of forming partially oxidized hydrocarbons from ethanes in which ethane gas contacts a two-part catalyst comprising a dehydrogenation portion and an oxide-ion conducting portion for a time and at a temperature sufficient to form an oxide. 4 figs.

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

1999-07-27T23:59:59.000Z

333

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

334

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

E-Print Network [OSTI]

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

Dennis, J A

1971-01-01T23:59:59.000Z

335

Molecular and Biochemical Characterization of Hydrocarbon Production in the Green Microalga Botryococcus braunii  

E-Print Network [OSTI]

Algae biofuels ................................................................................ 1 Algae .............................................................................................. 2 Botryococcus braunii... ..................................................................... 4 General biology ........................................................................ 4 Biofuel potential ....................................................................... 9 Hydrocarbon synthesis...

Weiss, Taylor Leigh

2012-10-19T23:59:59.000Z

336

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

337

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

338

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

339

Spectroscopic detection of Carbon Monoxide in the Young Supernova Remnant Cassiopeia A  

E-Print Network [OSTI]

We report the detection of carbon monoxide (CO) emission from the young supernova remnant Cassiopeia A (Cas A) at wavelengths corresponding to the fundamental vibrational mode at 4.65 micron. We obtained AKARI Infrared Camera spectra towards 4 positions which unambiguously reveal the broad characteristic CO ro-vibrational band profile. The observed positions include unshocked ejecta at the center, indicating that CO molecules form in the ejecta at an early phase. We extracted a dozen spectra across Cas A along the long 1 arcmin slits, and compared these to simple CO emission models in Local Thermodynamic Equilibrium to obtain first-order estimates of the excitation temperatures and CO masses involved. Our observations suggest that significant amounts of carbon may have been locked up in CO since the explosion 330 years ago. Surprisingly, CO has not been efficiently destroyed by reactions with ionized He or the energetic electrons created by the decay of the radiative nuclei. Our CO detection thus implies that...

Rho, Jeonghee; Cami, Jan; Reach, William

2012-01-01T23:59:59.000Z

340

Simultaneous Detection of Water, Methane and Carbon Monoxide in the Atmosphere of Exoplanet HR8799b  

E-Print Network [OSTI]

Absorption lines from water, methane and carbon monoxide are detected in the atmosphere of exoplanet HR8799b. A medium-resolution spectrum presented here shows well-resolved and easily identified spectral features from all three molecules across the K band. The majority of the lines are produced by CO and H2O, but several lines clearly belong to CH4. Comparisons between these data and atmosphere models covering a range of temperatures and gravities yield log mole fractions of H2O between -3.09 and -3.91, CO between -3.30 and -3.72 and CH4 between -5.06 and -5.85. More precise mole fractions are obtained for each temperature and gravity studied. A reanalysis of H-band data, previously obtained at similar spectral resolution, results in a nearly identical water abundance as determined from the K-band spectrum. The methane abundance is shown to be sensitive to vertical mixing and indicates an eddy diffusion coefficient in the range of 10^6 to 10^8 cm^2 s^-1, comparable to mixing in the deep troposphere of Jupite...

Barman, Travis S; Macintosh, Bruce; Marois, Christian

2015-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

Search for the electric dipole moment of the electron with thorium monoxide  

E-Print Network [OSTI]

The electric dipole moment of the electron (eEDM) is a signature of CP-violating physics beyond the Standard Model. We describe an ongoing experiment to measure or set improved limits to the eEDM, using a cold beam of thorium monoxide (ThO) molecules. The metastable $H {}^3\\Delta_1$ state in ThO has important advantages for such an experiment. We argue that the statistical uncertainty of an eEDM measurement could be improved by as much as 3 orders of magnitude compared to the current experimental limit, in a first-generation apparatus using a cold ThO beam. We describe our measurements of the $H$ state lifetime and the production of ThO molecules in a beam, which provide crucial data for the eEDM sensitivity estimate. ThO also has ideal properties for the rejection of a number of known systematic errors; these properties and their implications are described.

Amar C. Vutha; Wesley C. Campbell; Yulia V. Gurevich; Nicholas R. Hutzler; Maxwell Parsons; David Patterson; Elizabeth Petrik; Benjamin Spaun; John M. Doyle; Gerald Gabrielse; David DeMille

2010-11-06T23:59:59.000Z

342

Relationship of respiratory symptoms and pulmonary function to tar, nicotine, and carbon monoxide yield of cigarettes  

SciTech Connect (OSTI)

The data from consecutive surveys of the Tucson Epidemiologic Study (1981-1988) were used to evaluate the relationship in cigarette smokers of respiratory symptoms and pulmonary function to tar, nicotine, and carbon monoxide (CO) yields of the cigarette. There were 690 subjects who reported smoking regularly in at least one survey, over age 15. After adjustment for intensity and duration of smoking and for depth of inhalation, the risk of chronic phlegm, cough, and dyspnea were not related to the tar and nicotine yields. In 414 subjects with pulmonary function tested in at least one of the three surveys the spirometric indices used were significantly related to the daily dose of tar, nicotine, and CO (product of the cigarette yield and daily number of cigarettes smoked). The effects were more pronounced for past than for current doses. However, the differentiation of pulmonary function due to various yields of cigarettes was small in comparison to the difference in pulmonary function between smokers and nonsmokers.

Krzyzanowski, M.; Sherrill, D.L.; Paoletti, P.; Lebowitz, M.D. (National Institute of Hygiene, Warsaw (Poland))

1991-02-01T23:59:59.000Z

343

Carbon monoxide oxidation over three different states of copper: Development of a model metal oxide catalyst  

SciTech Connect (OSTI)

Carbon monoxide oxidation was performed over the three different oxidation states of copper -- metallic (Cu), copper (I) oxide (Cu{sub 2}O), and copper (II) oxide (CuO) as a test case for developing a model metal oxide catalyst amenable to study by the methods of modern surface science and catalysis. Copper was deposited and oxidized on oxidized supports of aluminum, silicon, molybdenum, tantalum, stainless steel, and iron as well as on graphite. The catalytic activity was found to decrease with increasing oxidation state (Cu > Cu{sub 2}O > CuO) and the activation energy increased with increasing oxidation state (Cu, 9 kcal/mol < Cu{sub 2}O, 14 kcal/mol < CuO, 17 kcal/mol). Reaction mechanisms were determined for the different oxidation states. Lastly, NO reduction by CO was studied. A Cu and CuO catalyst were exposed to an equal mixture of CO and NO at 300--350 C to observe the production of N{sub 2} and CO{sub 2}. At the end of each reaction, the catalyst was found to be Cu{sub 2}O. There is a need to study the kinetics of this reaction over the different oxidation states of copper.

Jernigan, G.G. [California Univ., Berkeley, CA (United States). Dept. of Chemistry; [Lawrence Berkeley Lab., CA (United States). Materials and Chemical Sciences Div.

1994-10-01T23:59:59.000Z

344

Separation of toxic metal ions, hydrophilic hydrocarbons, hydrophobic fuel and halogenated hydrocarbons and recovery of ethanol from a process stream  

DOE Patents [OSTI]

This invention provides a process to tremendously reduce the bulk volume of contaminants obtained from an effluent stream produced subsurface remediation. The chemicals used for the subsurface remediation are reclaimed for recycling to the remediation process. Additional reductions in contaminant bulk volume are achieved by the ultra-violet light destruction of halogenated hydrocarbons, and the complete oxidation of hydrophobic fuel hydrocarbons and hydrophilic hydrocarbons. The contaminated bulk volume will arise primarily from the disposal of the toxic metal ions. The entire process is modular, so if there are any technological breakthroughs in one or more of the component process modules, such modules can be readily replaced.

Kansa, Edward J. (Livermore, CA); Anderson, Brian L. (Lodi, CA); Wijesinghe, Ananda M. (Tracy, CA); Viani, Brian E. (Oakland, CA)

1999-01-01T23:59:59.000Z

345

Separation of toxic metal ions, hydrophilic hydrocarbons, hydrophobic fuel and halogenated hydrocarbons and recovery of ethanol from a process stream  

DOE Patents [OSTI]

This invention provides a process to tremendously reduce the bulk volume of contaminants obtained from an effluent stream produced subsurface remediation. The chemicals used for the subsurface remediation are reclaimed for recycling to the remediation process. Additional reductions in contaminant bulk volume are achieved by the ultra-violet light destruction of halogenated hydrocarbons, and the complete oxidation of hydrophobic fuel hydrocarbons and hydrophilic hydrocarbons. The contaminated bulk volume will arise primarily from the disposal of the toxic metal ions. The entire process is modular, so if there are any technological breakthroughs in one or more of the component process modules, such modules can be readily replaced. 3 figs.

Kansa, E.J.; Anderson, B.L.; Wijesinghe, A.M.; Viani, B.E.

1999-05-25T23:59:59.000Z

346

Learning about ozone depletion Paul J. Crutzen & Michael Oppenheimer  

E-Print Network [OSTI]

Learning about ozone depletion Paul J. Crutzen & Michael Oppenheimer Received: 12 January 2007 Mainz, Germany M. Oppenheimer (*) Department of Geosciences, Princeton University, Princeton, NJ 08544, USA e-mail: omichael@princeton.edu M. Oppenheimer Woodrow Wilson School of Public and International

Oppenheimer, Michael

347

Mathematical modeling of solid oxide fuel cells using hydrocarbon fuels  

E-Print Network [OSTI]

Solid oxide fuel cells (SOFCs) are high efficiency conversion devices that use hydrogen or light hydrocarbon (HC) fuels in stationary applications to produce quiet and clean power. While successful, HC-fueled SOFCs face ...

Lee, Won Yong, Ph. D. Massachusetts Institute of Technology

2012-01-01T23:59:59.000Z

348

Faults as potential hydrocarbon barriers, Arroyo Grande, California  

E-Print Network [OSTI]

Faulting in a sandstone introduces properties which are different from the country rock. Previous work has shown that these new properties can significantly impede the flow of hydrocarbons through the country rock. This thesis seeks to analyze...

Switek, Daniel Paul

1994-01-01T23:59:59.000Z

349

Effect of the Composition of Hydrocarbon Streams on HCCI Performance  

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

of hydrocarbon samples and can be treated as compositional variables which could describe bulk properties of the samples Sample fingerprint STEP 1: Data receiving Q(2d)RPR How...

350

Biodegradability of select polycyclic aromatic hydrocarbon (pah) mixtures  

E-Print Network [OSTI]

Polycyclic aromatic hydrocarbons (PAHs) are environmentally significant because of their ubiquity and the toxicity of some. Their recalcitrance and persistence makes them problematic environmental contaminants. Microbial degradation is considered...

Desai, Anuradha M.

2007-04-25T23:59:59.000Z

351

aromatic hydrocarbon emissions: Topics by E-print Network  

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

15 16 17 18 19 20 21 22 23 24 25 Next Page Last Page Topic Index 1 Detection of mid-infrared Aromatic Hydrocarbon Emission Features from the Small Magellanic Cloud Astrophysics...

352

aromatic hydrocarbon emission: Topics by E-print Network  

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

15 16 17 18 19 20 21 22 23 24 25 Next Page Last Page Topic Index 1 Detection of mid-infrared Aromatic Hydrocarbon Emission Features from the Small Magellanic Cloud Astrophysics...

353

Process for conversion of lignin to reformulated hydrocarbon gasoline  

DOE Patents [OSTI]

A process for converting lignin into high-quality reformulated hydrocarbon gasoline compositions in high yields is disclosed. The process is a two-stage, catalytic reaction process that produces a reformulated hydrocarbon gasoline product with a controlled amount of aromatics. In the first stage, a lignin material is subjected to a base-catalyzed depolymerization reaction in the presence of a supercritical alcohol as a reaction medium, to thereby produce a depolymerized lignin product. In the second stage, the depolymerized lignin product is subjected to a sequential two-step hydroprocessing reaction to produce a reformulated hydrocarbon gasoline product. In the first hydroprocessing step, the depolymerized lignin is contacted with a hydrodeoxygenation catalyst to produce a hydrodeoxygenated intermediate product. In the second hydroprocessing step, the hydrodeoxygenated intermediate product is contacted with a hydrocracking/ring hydrogenation catalyst to produce the reformulated hydrocarbon gasoline product which includes various desirable naphthenic and paraffinic compounds.

Shabtai, Joseph S. (Salt Lake City, UT); Zmierczak, Wlodzimierz W. (Salt Lake City, UT); Chornet, Esteban (Golden, CO)

1999-09-28T23:59:59.000Z

354

Process for converting light alkanes to higher hydrocarbons  

DOE Patents [OSTI]

A process is disclosed for the production of aromatic-rich, gasoline boiling range hydrocarbons from the lower alkanes, particularly from methane. The process is carried out in two stages. In the first, alkane is reacted with oxygen and hydrogen chloride over an oxyhydrochlorination catalyst such as copper chloride with minor proportions of potassium chloride and rare earth chloride. This produces an intermediate gaseous mixture containing water and chlorinated alkanes. The chlorinated alkanes are contacted with a crystalline aluminosilicate catalyst in the hydrogen or metal promoted form to produce gasoline range hydrocarbons with a high proportion of aromatics and a small percentage of light hydrocarbons (C.sub.2 -C.sub.4). The light hydrocarbons can be recycled for further processing over the oxyhydrochlorination catalyst.

Noceti, Richard P. (Pittsburgh, PA); Taylor, Charles E. (Pittsburgh, PA)

1988-01-01T23:59:59.000Z

355

Hydrocarbon Inhibition and HC Storage Modeling in Fe-Zeolite...  

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

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

356

Determination of Total Petroleum Hydrocarbons (TPH) Using Total Carbon Analysis  

SciTech Connect (OSTI)

Several methods have been proposed to replace the Freon(TM)-extraction method to determine total petroleum hydrocarbon (TPH) content. For reasons of cost, sensitivity, precision, or simplicity, none of the replacement methods are feasible for analysis of radioactive samples at our facility. We have developed a method to measure total petroleum hydrocarbon content in aqueous sample matrixes using total organic carbon (total carbon) determination. The total carbon content (TC1) of the sample is measured using a total organic carbon analyzer. The sample is then contacted with a small volume of non-pokar solvent to extract the total petroleum hydrocarbons. The total carbon content of the resultant aqueous phase of the extracted sample (TC2) is measured. Total petroleum hydrocarbon content is calculated (TPH = TC1-TC2). The resultant data are consistent with results obtained using Freon(TM) extraction followed by infrared absorbance.

Ekechukwu, A.A.

2002-05-10T23:59:59.000Z

357

Cooling and solidification of heavy hydrocarbon liquid streams  

DOE Patents [OSTI]

A process and apparatus for cooling and solidifying a stream of heavy hydrocarbon material normally boiling above about 850.degree. F., such as vacuum bottoms material from a coal liquefaction process. The hydrocarbon stream is dropped into a liquid bath, preferably water, which contains a screw conveyor device and the stream is rapidly cooled, solidified and broken therein to form discrete elongated particles. The solid extrudates or prills are then dried separately to remove substantially all surface moisture, and passed to further usage.

Antieri, Salvatore J. (Trenton, NJ); Comolli, Alfred G. (Yardley, PA)

1983-01-01T23:59:59.000Z

358

Catalytic Upgrading of Sugars to Hydrocarbons Technology Pathway  

SciTech Connect (OSTI)

This technology pathway case investigates the catalytic conversion of solubilized carbohydrate streams to hydrocarbon biofuels, utilizing data from recent efforts within the National Advanced Biofuels Consortium (NABC) in collaboration with Virent, Inc. Technical barriers and key research needs that should be pursued for the catalytic conversion of sugars pathway to be competitive with petroleum-derived gasoline-, diesel-, and jet-range hydrocarbon blendstocks have been identified.

Biddy, M.; Jones, S.

2013-03-01T23:59:59.000Z

359

Origin of gaseous hydrocarbons in east-central Texas groundwaters  

E-Print Network [OSTI]

; Follett, 1974). The high transmissivity and sandy lithology of the Sparta are much like those of the Queen City, as is the quality of water. 40 LIGNITE STREAKS 30 Laminated and discontinuous lenticular. Trough cross bedded siltstones. 20 ROAD l... hydrocarbons simply reflects a difference in the 5 C of the substrate. Sparta lignite is about 7%%do enriched in ' C relative to Yegua lignite, comparable to the difference seen in the gaseous hydrocarbons. ACKNOWLEDGMENTS I would like to thank Dr. Steven...

Coffman, Bryan Keith

1988-01-01T23:59:59.000Z

360

Emission of polycyclic aromatic hydrocarbons in China  

SciTech Connect (OSTI)

Emission of 16 polycyclic aromatic hydrocarbons (PAHs) listed as U.S. Environmental Protection Agency (U.S. EPA) priority pollutants from major sources in China were compiled. Geographical distribution and temporal change of the PAH emission, as well as emission profiles, are discussed. It was estimated that the total PAH emission in China was 25,300 tons in 2003. The emission profile featured a relatively higher portion of high molecular weight (HMW) species with carcinogenic potential due to large contributions of domestic coal and coking industry. Among various sources, biomass burning, domestic coal combustion, and the coking industry contributed 60%, 20%, and 16% of the total emission, respectively. Total emission, emission density, emission intensity, and emission per capita showed geographical variations. In general, the southeastern provinces were characterized by higher emission density, while those in western and northern China featured higher emission intensity and population-normalized emission. Although energy consumption in China went up continuously during the past two decades, annual emission of PAHs fluctuated depending on the amount of domestic coal consumption, coke production, and the efficiency of energy utilization. 47 refs., 6 figs.

Shanshan Xu; Wenxin Liu; Shu Tao [Peking University, Beijing (China). Laboratory for Earth Surface Processes, College of Environmental Sciences

2006-02-01T23:59:59.000Z

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

Rock types, pore types, and hydrocarbon exploration  

SciTech Connect (OSTI)

A proposed exploration-oriented method of classifying porosity in sedimentary rocks is based on microscopic examination cores or cuttings. Factors include geometry, size, abundance, and connectivity of the pores. The porosity classification is predictive of key petrophysical characteristics: porosity-permeability relationships, capillary pressures, and (less certainly) relative permeabilities. For instance, intercrystalline macroporosity typically is associated with high permeability for a given porosity, low capillarity, and favorable relative permeabilities. This is found to be true whether this porosity type occurs in a sucrosic dolomite or in a sandstone with pervasive quartz overgrowths. This predictive method was applied in three Rocky Mountain oil plays. Subtle pore throat traps could be recognized in the J sandstone (Cretaceous) in the Denver basin of Colorado by means of porosity permeability plotting. Variations in hydrocarbon productivity from a Teapot Formation (Cretaceous) field in the Powder River basin of Wyoming were related to porosity types and microfacies; the relationships were applied to exploration. Rock and porosity typing in the Red River Formation (Ordovician) reconciled apparent inconsistencies between drill-stem test, log, and mud-log data from a Williston basin wildcat. The well was reevaluated and completed successfully, resulting in a new field discovery. In each of these three examples, petrophysics was fundamental for proper evaluation of wildcat wells and exploration plays.

Coalson, E.B.; Hartmann, D.J.; Thomas, J.B.

1985-05-01T23:59:59.000Z

362

Tailoring hydrocarbon streams for asphaltene removal  

SciTech Connect (OSTI)

Oilfield production is often hindered by asphaltene precipitation which tends to fill the pores of the reservoir rocks and plug the wellbore tubing as well as the other auxiliary equipment used during crude oil recovery. Several remedies to remove these deposits have been proposed and patented but the injection of aromatic solvents such as toluene and light petroleum distillates is normally preferred. Previous studies with a number of pure aromatic hydrocarbons have shown that the solvent capacity of these molecules may be very different and that the degree of condensation plays an important role. In this regard, tetralins and naphthalenes are superior to alkylbenzenes. However, because the use of pure compounds is not economically feasible, the authors examined various industrial streams and the authors correlated their chemical composition to the solvent capacity. This work allowed the identification of the pseudo-components whose relative concentration is crucial for evaluating the solvent performances. Based on these data, the authors were able to find new products with ideal characteristics. The efficiency of one of these products was confirmed by the analysis of the data obtained when using this new solvent to remove asphaltene in damaged wells of an Italian field.

Del Bianco, A.; Stroppa, F.; Bertero, L.

1995-11-01T23:59:59.000Z

363

The Exposure-Response Curve for Ozone and Risk of Mortality and the Adequacy of Current Ozone  

E-Print Network [OSTI]

and applied several statistical models to data on air pollution, weather, and mortality for 98 U.S. urban mortality. Interventions to further reduce ozone pollution would benefit public health, even in regions pollutant linked to numerous harmful health effects, including reduced lung function, increased frequency

Dominici, Francesca

364

Supplement of "Inversion of and emissions  

E-Print Network [OSTI]

' $ 9 -pinene @ ¤ ¦ other hydrocarbons ¦§ carbon monoxide ¦ ¤ % ¤ methanol ¦ ¤ ¡¥ formaldehyde¦ ¤ ¥¨ ¦ ¤ `$ dimethyl sulfide ¦§¨ ¡ carbon disulfide ¤ ¡¥¨ hydrogen sulfide 7 E $ oxygen atom (excited state ppbv hydrogen £ ¡¥ : 311 ppbv nitrous oxide ¦§ ©¨ : 0.5 ppbv carbonyl sulfide ozone ¤ ¡¥ ©¡ hydrogen

Meskhidze, Nicholas

365

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

366

Kidney cancer and hydrocarbon exposures among petroleum refinery workers  

SciTech Connect (OSTI)

To evaluate the hypothesis of increased kidney cancer risk after exposure to hydrocarbons, especially those present in gasoline, we conducted a case-control study in a cohort of approximately 100,000 male refinery workers from five petroleum companies. A review of 18,323 death certificates identified 102 kidney cancer cases, to each of whom four controls were matched by refinery location and decade of birth. Work histories, containing an average of 15.7 job assignments per subject, were found for 98% of the cases and 94% of the controls. Tb each job, industrial hygienists assigned semiquantitative ratings for the intensity and frequency of exposures to three hydrocarbon categories: nonaromatic liquid gasoline distillates, aromatic hydrocarbons, and the more volatile hydrocarbons. Ratings of {open_quotes}present{close_quotes} or {open_quotes}absent{close_quotes} were assigned for seven additional exposures: higher boiling hydrocarbons, polynuclear aromatic hydrocarbons, asbestos, chlorinated solvents, ionizing radiation, and lead. Each exposure had either no association or a weak association with kidney cancer. For the hydrocarbon category of principal a priori interest, the nonaromatic liquid gasoline distillates, the estimated relative risk (RR) for any exposure above refinery background was 1.0 (95% confidence interval [CI] 0.5-1.9). Analyses of cumulative exposures and of exposures in varying time periods before kidney cancer occurrence also produced null or near-null results. In an analysis of the longest job held by each subject (average duration 9.2 years or 40% of the refiner&y work history), three groups appeared to be at increased risk: laborers (RR = 1.9,95% CI 1.0-3.9); workers in receipt, storage, and movements (RR = 2.5,95% CI 0.9-6.6); and unit cleaners (RR = 2.3, 95% CI 0.5-9.9). 53 refs., 7 tabs.

Poole, C.; Dreyer, N.A.; Satterfield, M.H. [Epidemiology Resources Inc., Newton Lower Falls, MA (United States); Levin, L. [Drexel Univ., Philadelphia, PA (United States)

1993-12-01T23:59:59.000Z

367

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

368

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

369

Preliminary assessment of hydrocarbon potential in southern Illinois  

SciTech Connect (OSTI)

Hydrocarbon exploration has been sparse south of the Cottage Grove fault system in southern Illinois. Over 240,000 ac in this area are within the Shawnee National Forest (SNF). Upcoming review of mineral exploration policy on SNF land and a recent amendment to the Mineral Leasing Act (1987) will result in release of portions of the SNF for competitive and potentially noncompetitive bidding for mineral exploration tracts in the near future. Preliminary assessment of hydrocarbon potential has been carried out in southern Illinois. Numerous oil shows occur in Paleozoic strata south of the Cottage Grove fault system, which, at present, describes the southern boundary of most oil production in Illinois. Only Mitchellsville oil field in southern Saline County lies south of the Cottage Grove fault system. The Upper Devonian New Albany Shale, though to be the primary source rock for Illinois basin hydrocarbons, underlies most of the area. Older potential source rocks may be present. Depositional trends of prolific oil-productive Mississippian strata in Illinois continue southward through the area. Few drill holes have tested strata older than Mississippian in the area. Complex faulting in the Rough Creek-Shawneetown fault system may have improved the potential for hydrocarbon emplacement and entrapment in this region. Preliminary assessment of hydrocarbon potential indicates that this wildcat region deserves further tests.

Crockett, J.E.; Oltz, D.F. (Illinois State Geological Survey, Champaign (USA))

1989-08-01T23:59:59.000Z

370

Scale-Up and Demonstration of Fly Ash Ozonation Technology  

SciTech Connect (OSTI)

The disposal of fly ash from the combustion of coal has become increasingly important. When the fly ash does not meet the required specification for the product or market intended, it is necessary to beneficiate it to achieve the desired quality. This project, conducted at PPL's Montour SES, is the first near full-scale ({approx}10 ton/day), demonstration of ash ozonation technology. Bituminous and sub bituminous ashes, including two ash samples that contained activated carbon, were treated during the project. Results from the tests were very promising. The ashes were successfully treated with ozone, yielding concrete-suitable ash quality. Preliminary process cost estimates indicate that capital and operating costs to treat unburned carbon are competitive with other commercial ash beneficiation technologies at a fraction of the cost of lost sales and/or ash disposal costs. This is the final technical report under DOE Cooperative Agreement No.: DE-FC26-03NT41730.

Rui Afonso; R. Hurt; I. Kulaots

2006-03-01T23:59:59.000Z

371

CF[sub 3] chemistry: Potential implications for stratospheric ozone  

SciTech Connect (OSTI)

The authors address questions about the chemistry of CF[sub 3] bearing compounds in the atmosphere, and the impact that the existence of and reaction rate constants for such species may have on stratospheric ozone. Species considered include CF[sub 3], CF[sub 3]O, CF[sub 3]O[sub 2], CF[sub 3]OH, CF[sub 3]OOH, CF[sub 3]ONO[sub 2], CF[sub 3]O[sub 2]NO[sub 2], and CF[sub 3]OOCl. Based on their calculational results, the authors suggest a number of experimental measurements which should substantially decrease uncertainties associated with the role of CF[sub 3] species in atmospheric chemistry related to ozone.

Ko, M.K.W.; Sze, N.D.; Rodriguez, J.M.; Weistenstein, D.K.; Heisey, C.W. (Atmospheric and Environmental Research, Inc., Cambridge, MA (United States)); Wayne, R.P.; Biggs, P.; Canosa-Mas, C.E. (Univ. of Oxford, Oxford (United Kingdom)); Sidebottom, H.W.; Treacy, J. (Univ. College, Dublin (Ireland))

1994-01-15T23:59:59.000Z

372

FORMATION OF MOLECULAR OXYGEN AND OZONE ON AMORPHOUS SILICATES  

SciTech Connect (OSTI)

Oxygen in the interstellar medium is seen in the gas phase, in ices (incorporated in H{sub 2}O, CO, and CO{sub 2}), and in grains such as (Mg{sub x} Fe{sub 1-x} )SiO{sub 3} or (Mg{sub x} Fe{sub 1-x} ){sub 2}SiO{sub 4}, 0 < x < 1. In this investigation, we study the diffusion of oxygen atoms and the formation of oxygen molecules and ozone on the surface of an amorphous silicate film. We find that ozone is formed at low temperature (<30 K), and molecular oxygen forms when the diffusion of oxygen atoms becomes significant, at around 60 K. This experiment, besides being the first determination of the diffusion energy barrier (1785 {+-} 35 K) for oxygen atoms on a silicate surface, suggests bare silicates as a possible storage place for oxygen atoms in low-A{sub v} environments.

Jing Dapeng; He Jiao; Vidali, Gianfranco [Physics Department, Syracuse University, Syracuse, NY 13244 (United States); Brucato, John Robert; Tozzetti, Lorenzo [Osservatorio Astrofisico di Arcetri, INAF, I-50125 Florence (Italy); De Sio, Antonio [Department of Physics and Astronomy, University of Florence, I-50125 Florence (Italy)

2012-09-01T23:59:59.000Z

373

Meeting the New Ozone Standard: Challenges and Opportunities  

Broader source: Energy.gov [DOE]

This presentation by Anna Garcia, executive director of the Ozone Transport Commission, was part of the July 2008 Webcast sponsored by the U.S. Department of Energy Office of Energy Efficiency and Renewable Energy Weatherization and Intergovernmental Program Clean Energy and Air Quality Integration Initiative that was titled Role of Energy Efficiency and Renewable Energy in Improving Air Quality and Addressing Greenhouse Gas Reduction Goals on High Electric Demand Days.

374

Hydrocarbon Processing`s HPI construction boxscore update  

SciTech Connect (OSTI)

Data are compiled for oil and gas industry construction projects worldwide, listing country (and state or province, when appropriate), company, location of the project, purpose, plant capacity, estimated cost, current status, licensor, engineering firm, and construction company. Projects include carbon monoxide, urea, ammonia, isomerizer, hydrogen, alkylation, TAME, desalter, hydrotreating, sulfur, waste gas cleanup, catalytic reformer, ethylene recovery, natural gas helium, nitrogen removal, NGL recovery, cumene, dewaxer, polystyrene, vinyl chloride, synthesis gas, formaldehyde, FCC cracker, isobutylene, H{sub 2}S removal, cogeneration, methanol, delayed coker, gas oil treater, NGL fractionation, BTX, information systems, control systems, waste water cleanup, glycol treater, acid gas removal, LPG, MTBE, caustic cleanup, visbreaker, naphtha treater, and others.

NONE

1996-02-01T23:59:59.000Z

375

E-Print Network 3.0 - arctic ozone loss Sample Search Results  

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

Chemistry Summary: stratospheric ozone losses during cold Arctic Januaries, M. Rex, R. J. Salaw- itch, M. L. Santee, J. W. Waters... , and UARS MLS to demonstrate that the...

376

E-Print Network 3.0 - atmospheric ozone depletion Sample Search...  

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

78992007 Summary: ozone depletion based on sequential assimilation of satellite data from the ENVISATMIPAS and Odin... 2007 Abstract. The objective of this study...

377

E-Print Network 3.0 - ambient ozone exposure Sample Search Results  

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

Materials Science ; Energy Storage, Conversion and Utilization 12 Proceedings of Healthy Buildings 2009 Paper 141 Removal of Indoor Ozone with Reactive Materials: Preliminary...

378

E-Print Network 3.0 - atmospheric ozone increases Sample Search...  

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

Collection: Environmental Sciences and Ecology ; Geosciences 78 Proceedings of Healthy Buildings 2009 Paper 336 Time-Scale Analysis for Reactive Deposition of Ozone via Passive...

379

E-Print Network 3.0 - ameliorate ozone effects Sample Search...  

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

Summary: students confuse the relationship between the ozone hole and the greenhouse effect, thus confusing... , and to suggest more effective teaching methods. 2....

380

E-Print Network 3.0 - analyzing ground ozone Sample Search Results  

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

are analyzed... to superposition of the "natural" pro- cesses. Comparison of the total ozone ... Source: Ecole Polytechnique, Centre de mathmatiques Collection:...

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

Catalytic Upgrading of Sugars to Hydrocarbons Technology Pathway  

SciTech Connect (OSTI)

In support of the Bioenergy Technologies Office, the National Renewable Energy Laboratory (NREL) and the Pacific Northwest National Laboratory (PNNL) are undertaking studies of biomass conversion technologies to hydrocarbon fuels to identify barriers and target research toward reducing conversion costs. Process designs and preliminary economic estimates for each of these pathway cases were developed using rigorous modeling tools (Aspen Plus and Chemcad). These analyses incorporated the best information available at the time of development, including data from recent pilot and bench-scale demonstrations, collaborative industrial and academic partners, and published literature and patents. This technology pathway case investigates the catalytic conversion of solubilized carbohydrate streams to hydrocarbon biofuels, utilizing data from recent efforts within the National Advanced Biofuels Consortium (NABC) in collaboration with Virent, Inc.. Technical barriers and key research needs that should be pursued for the catalytic conversion of sugars pathway to be competitive with petroleum-derived gasoline, diesel and jet range hydrocarbon blendstocks have been identified.

Biddy, Mary J.; Jones, Susanne B.

2013-03-31T23:59:59.000Z

382

Process for light-driven hydrocarbon oxidation at ambient temperatures  

DOE Patents [OSTI]

A photochemical reaction for the oxidation of hydrocarbons uses molecular oxygen as the oxidant. A reductive photoredox cycle that uses a tin(IV)- or antimony(V)-porphyrin photosensitizer generates the reducing equivalents required to activate oxygen. This artificial photosynthesis system drives a catalytic cycle, which mimics the cytochrome P.sub.450 reaction, to oxidize hydrocarbons. An iron(III)- or manganese(III)-porphyrin is used as the hydrocarbon-oxidation catalyst. Methylviologen can be used as a redox relay molecule to provide for electron-transfer from the reduced photosensitizer to the Fe or Mn porphyrin. The system is long-lived and may be used in photo-initiated spectroscopic studies of the reaction to determine reaction rates and intermediates.

Shelnutt, John A. (Tijeras, NM)

1990-01-01T23:59:59.000Z

383

Combustion process for synthesis of carbon nanomaterials from liquid hydrocarbon  

DOE Patents [OSTI]

The present invention provides a combustion apparatus for the production of carbon nanomaterials including fullerenes and fullerenic soot. Most generally the combustion apparatus comprises one or more inlets for introducing an oxygen-containing gas and a hydrocarbon fuel gas in the combustion system such that a flame can be established from the mixed gases, a droplet delivery apparatus for introducing droplets of a liquid hydrocarbon feedstock into the flame, and a collector apparatus for collecting condensable products containing carbon nanomaterials that are generated in the combustion system. The combustion system optionally has a reaction zone downstream of the flame. If this reaction zone is present the hydrocarbon feedstock can be introduced into the flame, the reaction zone or both.

Diener, Michael D.; Alford, J. Michael; Nabity, James; Hitch, Bradley D.

2007-01-02T23:59:59.000Z

384

Method for recovering light hydrocarbons from coal agglomerates  

DOE Patents [OSTI]

A method and apparatus for removing light hydrocarbons, such as heptane, from coal agglomerates includes an enclosed chamber having a substantially horizontal perforate surface therein. The coal agglomerates are introduced into a water bath within the chamber. The agglomerates are advanced over the surface while steam is substantially continuously introduced through the surface into the water bath. Steam heats the water and causes volatilization of the light hydrocarbons, which may be collected from the overhead of the chamber. The resulting agglomerates may be collected at the opposite end from the surface and subjected to final draining processes prior to transportation or use.

Huettenhain, Horst (Benicia, CA); Benz, August D. (Hillsborough, CA); Getsoian, John (Ann Arbor, MI)

1991-01-01T23:59:59.000Z

385

Upgrading of petroleum oil feedstocks using alkali metals and hydrocarbons  

DOE Patents [OSTI]

A method of upgrading an oil feedstock by removing heteroatoms and/or one or more heavy metals from the oil feedstock composition. This method reacts the oil feedstock with an alkali metal and an upgradant hydrocarbon. The alkali metal reacts with a portion of the heteroatoms and/or one or more heavy metals to form an inorganic phase separable from the organic oil feedstock material. The upgradant hydrocarbon bonds to the oil feedstock material and increases the number of carbon atoms in the product. This increase in the number of carbon atoms of the product increases the energy value of the resulting oil feedstock.

Gordon, John Howard

2014-09-09T23:59:59.000Z

386

Low-Temperature Catalytic Process To Produce Hydrocarbons From Sugars  

DOE Patents [OSTI]

Disclosed is a method of producing hydrogen from oxygenated hydrocarbon reactants, such as methanol, glycerol, sugars (e.g. glucose and xylose), or sugar alcohols (e.g. sorbitol). The method takes place in the condensed liquid phase. The method includes the steps of reacting water and a water-soluble oxygenated hydrocarbon in the presence of a metal-containing catalyst. The catalyst contains a metal selected from the group consisting of Group VIIIB transitional metals, alloys thereof, and mixtures thereof. The disclosed method can be run at lower temperatures than those used in the conventional steam reforming of alkanes.

Cortright, Randy D. (Madison, WI); Dumesic, James A. (Verona, WI)

2005-11-15T23:59:59.000Z

387

Electrically heated particulate filter regeneration using hydrocarbon adsorbents  

DOE Patents [OSTI]

An exhaust system that processes exhaust generated by an engine is provided. The system generally includes a particulate filter (PF) that filters particulates from the exhaust wherein an upstream end of the PF receives exhaust from the engine. A grid of electrically resistive material selectively heats exhaust passing through the upstream end to initiate combustion of particulates within the PF. A hydrocarbon adsorbent coating applied to the PF releases hydrocarbons into the exhaust to increase a temperature of the combustion of the particulates within the PF.

Gonze, Eugene V [Pinckney, MI

2011-02-01T23:59:59.000Z

388

Hydrocarbon composition of crude oil from Lam Bank  

SciTech Connect (OSTI)

The authors discuss the crude oil from a new offshore field called the Lam Bank in the Caspian Sea. A segregated commercial crude was distilled and the distillation data is shown. In order to determine the content of n-paraffins, the naphthenic-paraffinic part of the narrow cuts was subjected to adsorptive separation on CaA zeolite. Owing to the high contents of naphthenic and isoparaffinic hydrocarbons and the low content of aromatic hydrocarbons in the distillate part, this crude can be used to produce high-quality fuels and oils by the use of the dewaxing processes.

Samedova, F.I.; Agaeva, R.M.; Alieva, F.Z.; Valiev, M.A.

1987-07-01T23:59:59.000Z

389

Method and apparatus for production of subsea hydrocarbon formations  

DOE Patents [OSTI]

A system for controlling, separating, processing and exporting well fluids produced from subsea hydrocarbon formations is disclosed. The subsea well tender system includes a surface buoy supporting one or more decks above the water surface for accommodating equipment to process oil, gas and water recovered from the subsea hydrocarbon formation. The surface buoy includes a surface-piercing central flotation column connected to one or more external flotation tanks located below the water surface. The surface buoy is secured to the sea bed by one or more tendons which are anchored to a foundation with piles imbedded in the sea bed. The system accommodates multiple versions on the surface buoy configuration. 20 figures.

Blandford, J.W.

1995-01-17T23:59:59.000Z

390

Method and apparatus for production of subsea hydrocarbon formations  

DOE Patents [OSTI]

A system for controlling, separating, processing and exporting well fluids produced from subsea hydrocarbon formations is disclosed. The subsea well tender system includes a surface buoy supporting one or more decks above the water surface for accommodating equipment to process oil, gas and water recovered from the subsea hydrocarbon formation. The surface buoy includes a surface-piercing central flotation column connected to one or more external floatation tanks located below the water surface. The surface buoy is secured to the seabed by one or more tendons which are anchored to a foundation with piles imbedded in the seabed. The system accommodates multiple versions on the surface buoy configuration.

Blandford, Joseph W. (15 Mott La., Houston, TX 77024)

1995-01-01T23:59:59.000Z

391

Method for determining processability of a hydrocarbon containing feedstock  

DOE Patents [OSTI]

Disclosed herein is a method involving the steps of (a) precipitating an amount of asphaltenes from a liquid sample of a first hydrocarbon-containing feedstock having solvated asphaltenes therein with one or more first solvents in a column; (b) determining one or more solubility characteristics of the precipitated asphaltenes; (c) analyzing the one or more solubility characteristics of the precipitated asphaltenes; and (d) correlating a measurement of feedstock reactivity for the first hydrocarbon-containing feedstock sample with a mathematical parameter derived from the results of analyzing the one or more solubility characteristics of the precipitated asphaltenes.

Schabron, John F.; Rovani, Jr., Joseph F.

2013-09-10T23:59:59.000Z

392

LiMnPO4 Nanoplate Grown via Solid-State Reaction in Molten Hydrocarbon...  

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

LiMnPO4 Nanoplate Grown via Solid-State Reaction in Molten Hydrocarbon for Li-ion Battery Cathode. LiMnPO4 Nanoplate Grown via Solid-State Reaction in Molten Hydrocarbon for Li-ion...

393

Oil & Chemical Pollution 6 (19'X)} 81-Hydrocarbon Pollution of  

E-Print Network [OSTI]

distribution offuel distillates is evident with only a small contribution from lubricating and heavier oilOil & Chemical Pollution 6 (19'X)} 81- pollution as all oils contain aromatic hydrocarbons while few, if any, biogenic aromatic hydrocarbons

Canberra, University of

394

Interpretation of side-scan sonar images from hydrocarbon seep areas of the Louisiana continental slope  

E-Print Network [OSTI]

Side-scan sonar images from the Louisiana continental slope were examined to study hydrocarbon seepage and related surficial geologic seafloor features. Three study areas are located in the Green Canyon area and the Garden Bank area. Hydrocarbon...

Hou, Rusheng

2001-01-01T23:59:59.000Z

395

Syngas Conversion to Gasoline-Range Hydrocarbons over Pd/ZnO...  

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

Syngas Conversion to Gasoline-Range Hydrocarbons over PdZnOAl2O3 and ZSM-5 Composite Catalyst System. Syngas Conversion to Gasoline-Range Hydrocarbons over PdZnOAl2O3 and ZSM-5...

396

Evaluation of biological treatment for the degradation of petroleum hydrocarbons in a wastewater treatment plant  

E-Print Network [OSTI]

present. An evaluation of the performance of the biological treatment of petroleum hydrocarbon by the hydrocarbon degrading microbes at the Brayton Fire School??s 4 million gallon per day (MGD) wastewater treatment plant was the main research objective...

Basu, Pradipta Ranjan

2005-08-29T23:59:59.000Z

397

Plasma Chemistry and Plasma Processing, Vol. 22, No. 4, December 2002 ( 2002) Ozone Production in the Positive DC Corona  

E-Print Network [OSTI]

Plasma Chemistry and Plasma Processing, Vol. 22, No. 4, December 2002 ( 2002) Ozone Production the distribution of ozone, but does not affect the rate of production. KEY WORDS: Corona discharge; corona plasma

Chen, Junhong

398

A 4D Synchrotron X-Ray-Tomography Study of the Formation of Hydrocarbon-  

E-Print Network [OSTI]

hydrocarbons and the growing production of hydrocarbons from low-permeability tight rocks. Quantitative models, University of Oslo, Idaho National Laboratory, and Institute for Energy Technology Summary Recovery of oil from oil shales and the natural primary migration of hydrocarbons are closely related processes

Mazzini, Adriano

399

UPTAKE AND LOSS OF PETROLEUM HYDROCARBONS BY THE MUSSEL, MYTILUS EDULIS, IN LABORATORY EXPERIMENTS  

E-Print Network [OSTI]

UPTAKE AND LOSS OF PETROLEUM HYDROCARBONS BY THE MUSSEL, MYTILUS EDULIS, IN LABORATORY EXPERIMENTS ROBERT C. CLARK, JR., AND JOHN S. FINLEY' ABSTRACT Petroleum paraffin hydrocarbons (n-CI4H30 to n-C37H76 system that simulated tides. The mussels were exposed to levels of petroleum hydrocarbons from a surface

400

192 IEEE SENSORS JOURNAL, VOL. 7, NO. 2, FEBRUARY 2007 Hydrocarbon and Fluorocarbon Monitoring by MIS  

E-Print Network [OSTI]

192 IEEE SENSORS JOURNAL, VOL. 7, NO. 2, FEBRUARY 2007 Hydrocarbon and Fluorocarbon Monitoring of hydrocarbon and fluorocarbon molecules on a Ni coil (CE), the products detectable by metal­ insulator Terms--Fluorocarbons, hydrocarbons, metal­ insulator­semiconductor (MIS) and metal

Moritz, Werner

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

Ground-based zenith sky abundances and in situ gas cross sections for ozone and nitrogen dioxide  

E-Print Network [OSTI]

Ground-based zenith sky abundances and in situ gas cross sections for ozone and nitrogen dioxide, in situ ambient absorption gas cell mea- surements for ozone and nitrogen dioxide, and ground-based zenith for ozone and nitrogen dioxide that are retrieved from measured spectra of the zenith sky

Dirksen, Ruud

402

Ensemble forecasting with machine learning algorithms for ozone, nitrogen dioxide and PM10 on the Prev'Air  

E-Print Network [OSTI]

Ensemble forecasting with machine learning algorithms for ozone, nitrogen dioxide and PM10'Air operational platform. This platform aims at forecasting maps, on a daily basis, for ozone, nitrogen dioxide models, ozone, nitrogen dioxide, particulate matter, threshold exceedance 1. Introduction1 Operational

Mallet, Vivien

403

Experimental study of reactions between ozone and building products M. Nicolas, O. Ramalho, F. Maupetit*  

E-Print Network [OSTI]

ozone and building products and document their potential impact on indoor air quality. PreliminaryExperimental study of reactions between ozone and building products M. Nicolas, O. Ramalho, F experiments were conducted on four building products: two carpets, a gypsum board and a pine wood board

Paris-Sud XI, Université de

404

Validation of Ozone Monitoring Instrument nitrogen dioxide columns E. A. Celarier,1  

E-Print Network [OSTI]

Validation of Ozone Monitoring Instrument nitrogen dioxide columns E. A. Celarier,1 E. J. Brinksma the standard nitrogen dioxide (NO2) data product (Version 1.0.), which is based on measurements made), Validation of Ozone Monitoring Instrument nitrogen dioxide columns, J. Geophys. Res., 113, D15S15, doi:10

405

Ground-level nitrogen dioxide concentrations inferred from the satellite-borne Ozone Monitoring Instrument  

E-Print Network [OSTI]

Ground-level nitrogen dioxide concentrations inferred from the satellite-borne Ozone Monitoring; published 28 August 2008. [1] We present an approach to infer ground-level nitrogen dioxide (NO2), Ground-level nitrogen dioxide concentrations inferred from the satellite-borne Ozone Monitoring

Martin, Randall

406

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

E-Print Network [OSTI]

Summary Satellite observations of ozone and nitrogen dioxide: from retrievals to emission estimates be inferred for important trace gases such as ozone (O3) and nitrogen dioxide (NO2). Chemical transport models.11 to 3.79. Total nitrogen dioxide columns can be retrieved from space in the 405­465 nm window

Haak, Hein

407

Tropospheric ozone trends at Mauna Loa Observatory tied to decadal climate variability  

E-Print Network [OSTI]

measurements at Mauna Loa Observatory in Hawaii reveal little change in tropospheric ozone levels during spring a suite of chemistry­climate model simulations. We show that the flow of ozone-rich air from Eurasia towards Hawaii during spring weakened in the 2000s as a result of La-Niña-like decadal cooling

408

PPPL-3281, Preprint: January 1998, UC-426 Synthesis of Ozone at Atmospheric Pressure  

E-Print Network [OSTI]

to ~250 ppm were produced using a thermal plasma reactor system based on an ICP torch operating at 2.5 MHz by rapid mixing of molecular oxygen with atomic oxygen produced by the torch. The ozone concentration in industrial processes is increasing. Applications for ozone include treatment of waste water, water

409

Separating the dynamical effects of climate change and ozone depletion. Part  

E-Print Network [OSTI]

) fixed at 1960 levels and ozone depleting substances (ODSs) varying in time, 2) ODSs fixed at 1960 levels averaged wave drag in SH spring and summer, as well as for final warming dates. Ozone depletion a significant impact on the stratosphere on both a global and a regional scale. Over the past three decades

Wirosoetisno, Djoko

410

Chapter Descriptions, Parties Request, and Timetable 2010 WMO/UNEP Ozone Assessment  

E-Print Network [OSTI]

AND SURFACE ULTRAVIOLET RADIATION CHAPTER 3: FUTURE OZONE AND ITS IMPACT ON SURFACE UV CHAPTER 4) of this 2010 ozone assessment. It provides updated information on degradation products which could have of understanding on ODS degradation products in the stratosphere (e.g., HCl, HF, BrO, CF2O), examines how

Jánosi, Imre M.

411

The Role of Material Porosity on Ozone Uptake for Metakaolin-Concrete Surfaces  

E-Print Network [OSTI]

to a diminished environmental impact, clay may cause increased removal of ozone, an important indoor pollutant velocity, Heterogeneous Chemistry, Construction Materials 1 Introduction Metakaolin-cement systems hold ozone uptake. Cement is an essential component in the building industry used in formulating concrete

Siegel, Jeffrey

412

Simultaneous retrievals of column ozone and aerosol optical properties from direct and diffuse solar irradiance measurements  

E-Print Network [OSTI]

of column ozone and aerosol optical properties from direct and diffuse solar irradiance measurements, JSimultaneous retrievals of column ozone and aerosol optical properties from direct and diffuse solar irradiance measurements Christian D. Goering,1 Tristan S. L'Ecuyer,1 Graeme L. Stephens,1 James R

Stephens, Graeme L.

413

Effects of Sodium Chloride Particles, Ozone, UV, and Relative Humidity on Atmospheric Corrosion of Silver  

E-Print Network [OSTI]

Effects of Sodium Chloride Particles, Ozone, UV, and Relative Humidity on Atmospheric Corrosion The corrosion of Ag contaminated with NaCl particles in gaseous environments containing humidity and ozone analyzed using a coulometric reduction technique. The atmospheric corrosion of Ag was greatly accelerated

414

Air Pollution Physics and Chemistry EAS 6790 Home Work Assignment Ozone Chemistry 2  

E-Print Network [OSTI]

1 Air Pollution Physics and Chemistry EAS 6790 Fall 2010 Home Work Assignment Ozone Chemistry 2 and Chemistry EAS 6790 Fall 2006 Home Work Assignment No. 4, Ozone Chemistry Problems 11.8 and 11.9 (sub-part 1 and 2 only). Daniel Jacob, Atmospheric Chemistry #12;2 Problem 2: 2 2. Consider an air parcel ventilated

Weber, Rodney

415

Can ozone depletion and global warming interact to produce rapid climate change?  

E-Print Network [OSTI]

Can ozone depletion and global warming interact to produce rapid climate change? Dennis L. Hartmann of Climate Change (IPCC) assess- ment of the status of global warming, which reported that winter stratospheric ozone depletion and greenhouse warming are possible. These interactions may be responsible

Limpasuvan, Varavut

416

NORTHEASTERN NATURALIST2009 16(2):307313 Variation in Ozone Sensitivity Within Indian Hemp and  

E-Print Network [OSTI]

NORTHEASTERN NATURALIST2009 16(2):307­313 Variation in Ozone Sensitivity Within Indian Hemp , and Dennis R. Decoteau1 Abstract - Sixteen selections of Apocynum cannabinum (Indian Hemp) and nine, adaxial stipple, similar to symptoms ascribed to ambient ozone in the field. Indian Hemp was more

Decoteau, Dennis R.

417

Surface ozone background in the United States: Canadian and Mexican pollution influences  

E-Print Network [OSTI]

of anthropogenic emissions from Canada, Mexico, and outside North America on daily maximum 8-hour average ozone Surface ozone Air quality standard Chemical transport model Global model a b s t r a c t We use a global chemical transport model (GEOS-Chem) with 1 Ã? 1 horizontal resolution to quantify the effects

Park, Rokjin

418

Stratospheric ozone depletion: a key driver of recent precipitation trends in South Eastern South America  

E-Print Network [OSTI]

. In this paper we focus on South Eastern South America (SESA), a region that has exhibited one of the largest South America 1 Introduction The depletion of ozone in the polar Antarctic strato- sphere (i.e. `theStratospheric ozone depletion: a key driver of recent precipitation trends in South Eastern South

419

Tropospheric ozone climatology over Irene, South Africa, from 1990 to 1994 and 1998 to 2002  

E-Print Network [OSTI]

Tropospheric ozone climatology over Irene, South Africa, from 1990 to 1994 and 1998 to 2002 R. D in South Africa are reported for the period 1990 to 1994 and a more recent period, 1998 to 2002, when), Tropospheric ozone climatology over Irene, South Africa, from 1990 to 1994 and 1998 to 2002, J. Geophys. Res

Thompson, Anne

420

Passive Ozone Control Through Use of Reactive Indoor Wall and Ceiling Materials  

E-Print Network [OSTI]

Passive Ozone Control Through Use of Reactive Indoor Wall and Ceiling Materials Paper # 715 Donna A and unpainted drywall as passive ozone control surfaces in a room-sized laboratory chamber. Mean deposition-50%, resulted in increased reactivity for activated carbon. In our model for a typical house, about 35

Siegel, Jeffrey

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

Fundamental spectroscopic studies of carbenes and hydrocarbon radicals  

SciTech Connect (OSTI)

Highly reactive carbenes and carbon-chain radicals are studied at millimeter wavelengths by observing their rotational spectra. The purpose is to provide definitive spectroscopic identification, accurate spectroscopic constants in the lowest vibrational states, and reliable structures of the key intermediates in reactions leading to aromatic hydrocarbons and soot particles in combustion.

Gottlieb, C.A.; Thaddeus, P. [Harvard Univ., Cambridge, MA (United States)

1993-12-01T23:59:59.000Z

422

Hydrocarbons Heterogeneous Pyrolysis: Experiments and Modeling for Scramjet Thermal Management  

E-Print Network [OSTI]

1 Hydrocarbons Heterogeneous Pyrolysis: Experiments and Modeling for Scramjet Thermal Management : United States (2008)" #12;2 I. Introduction One of the main issues of the development of scramjet, an air to the endothermicity of its thermal decomposition. Because of the large heat load found in a scramjet, engine

Paris-Sud XI, Université de

423

Hydrocarbon saturation determination using acoustic velocities obtained through casing  

DOE Patents [OSTI]

Compressional and shear velocities of earth formations are measured through casing. The determined compressional and shear velocities are used in a two component mixing model to provides improved quantitative values for the solid, the dry frame, and the pore compressibility. These are used in determination of hydrocarbon saturation.

Moos, Daniel (Houston, TX)

2010-03-09T23:59:59.000Z

424

Formation mechanism for polycyclic aromatic hydrocarbons in methane flames  

E-Print Network [OSTI]

Formation mechanism for polycyclic aromatic hydrocarbons in methane flames K. Siegmanna) Swiss 96822 Received 24 August 1999; accepted 13 October 1999 A laminar diffusion flame of methane exhausts,7­17 coal-fired, electricity generating power plants,18,19 tobacco smoke,20 residential wood

Sattler, Klaus

425

THERMOCATALYTIC CO2-FREE PRODUCTION OF HYDROGEN FROM HYDROCARBON FUELS  

E-Print Network [OSTI]

THERMOCATALYTIC CO2- FREE PRODUCTION OF HYDROGEN FROM HYDROCARBON FUELS N. Muradov Florida Solar Energy Center 1679 Clearlake Road, Cocoa, Florida 32922 tel. 321-638-1448, fax. 321-638-1010, muradov (except for the start-up operation). This results in the following advantages: (1) no CO/CO2 byproducts

426

Chemical Kinetics of Hydrocarbon Ignition in Practical Combustion Systems  

SciTech Connect (OSTI)

Chemical kinetic factors of hydrocarbon oxidation are examined in a variety of ignition problems. Ignition is related to the presence of a dominant chain branching reaction mechanism that can drive a chemical system to completion in a very short period of time. Ignition in laboratory environments is studied for problems including shock tubes and rapid compression machines. Modeling of the laboratory systems are used to develop kinetic models that can be used to analyze ignition in practical systems. Two major chain branching regimes are identified, one consisting of high temperature ignition with a chain branching reaction mechanism based on the reaction between atomic hydrogen with molecular oxygen, and the second based on an intermediate temperature thermal decomposition of hydrogen peroxide. Kinetic models are then used to describe ignition in practical combustion environments, including detonations and pulse combustors for high temperature ignition, and engine knock and diesel ignition for intermediate temperature ignition. The final example of ignition in a practical environment is homogeneous charge, compression ignition (HCCI) which is shown to be a problem dominated by the kinetics intermediate temperature hydrocarbon ignition. Model results show why high hydrocarbon and CO emissions are inevitable in HCCI combustion. The conclusion of this study is that the kinetics of hydrocarbon ignition are actually quite simple, since only one or two elementary reactions are dominant. However, there are many combustion factors that can influence these two major reactions, and these are the features that vary from one practical system to another.

Westbrook, C.K.

2000-07-07T23:59:59.000Z

427

Chlorinated Hydrocarbon Levels in Fishes and Shellfishes of the  

E-Print Network [OSTI]

the utilization by humans of the vast protein resources in the sea. Chlorinated hydrocarbons from both agricultural and industrial chemicals have been found repeatedly in marine organisms throughout the world also analyzed a few samples of fish eggs, liver. oil. and meal. Finfishes from the northeastern Pacific

428

Energy Conservation Opportunities in Hydrocarbon Resin Manufacturing Facilities  

E-Print Network [OSTI]

"The results of a plant-wide assessment of the manufacturing facilities of Neville Chemical Company, a manufacturer of hydrocarbon resins will be presented in this paper. The project was co-funded by US Department of Energy under its Plant...

Ganji, A. R.; Hackett, B.; Chow, S.; Lonergan, R.; Wimer, J.

429

Theoretical studies of hydrocarbon combustion chemistry. Annual progress report  

SciTech Connect (OSTI)

The author reports here the results of DZP CISD calculations for methylcarbene. Geometry, symmetry, and vibrational modes for the radical are reported for both the singlet and the triplet state. Future work will focus on the ethyl radical-oxygen interaction relevant to hydrocarbon combustion.

Schaefer, H.F. III

1994-08-01T23:59:59.000Z

430

FROM INTERSTELLAR POLYCYCLIC AROMATIC HYDROCARBONS AND ICE TO ASTROBIOLOGY  

E-Print Network [OSTI]

photolysis of these ices produces a host of new compounds, some of which show intriguing prebiotic behavior1 FROM INTERSTELLAR POLYCYCLIC AROMATIC HYDROCARBONS AND ICE TO ASTROBIOLOGY LOUIS J. ALLAMANDOLA, the concept of ices in dense molecular clouds ignored, and the notion of large, abundant, gas phase, carbon

431

RICH METHANE PREMIXED LAMINAR FLAMES DOPED BY LIGHT UNSATURATED HYDROCARBONS  

E-Print Network [OSTI]

RICH METHANE PREMIXED LAMINAR FLAMES DOPED BY LIGHT UNSATURATED HYDROCARBONS PART III: CYCLOPENTENE-length article SHORTENED RUNNING TITLE : METHANE FLAMES DOPED BY CYCLOPENTENE * E-mail : pierre with the studies presented in the parts I and II of this paper, the structure of a laminar rich premixed methane

Paris-Sud XI, Université de

432

RICH METHANE PREMIXED LAMINAR FLAMES DOPED BY LIGHT UNSATURATED HYDROCARBONS  

E-Print Network [OSTI]

RICH METHANE PREMIXED LAMINAR FLAMES DOPED BY LIGHT UNSATURATED HYDROCARBONS PART I: ALLENE Full-length article SHORTENED RUNNING TITLE : METHANE FLAMES DOPED BY ALLENE OR PROPYNE * E investigated: a pure methane flame and two methane flames doped by allene and propyne, respectively. The gases

Paris-Sud XI, Université de

433

RICH METHANE PREMIXED LAMINAR FLAMES DOPED BY LIGHT UNSATURATED HYDROCARBONS  

E-Print Network [OSTI]

RICH METHANE PREMIXED LAMINAR FLAMES DOPED BY LIGHT UNSATURATED HYDROCARBONS PART II: 1,3-BUTADIENE-length article SHORTENED RUNNING TITLE : METHANE FLAMES DOPED BY 1,3-BUTADIENE * E-mail : Pierre of this paper, the structure of a laminar rich premixed methane flame doped with 1,3-butadiene has been

Paris-Sud XI, Université de

434

The toxicity of certain new chlorinated hydrocarbons to cotton pests  

E-Print Network [OSTI]

THE TOXICITY OF CERTAIN NEW CHLORINATED HYDROCARBONS TO COTTON PESTS A Dissertation 5y MARVIN EUGENE MERKL Approved as to style and content by: Chairman of CouBlttee Head of Departnent May 19*3 THE TOXICITY OF CERTAIN NEW CHLORINATED... .....................................................78 CONCLUSIONS............................................... ..81 BIBLIOGRAPHI .............................................. ..82 Pag? FIGURES 1* Dosage-?ortality curve for the toxicity of endrin to aphids...

Merkl, Marvin Eugene

1953-01-01T23:59:59.000Z

435

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]

), or with air and steam (autothermal reforming or ATR), to convert gasoline, methanol or other hydrocarbons

Azad, Abdul-Majeed

436

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

437

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.

438

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

439

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

440

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

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

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

442

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

443

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

444

Moving hydrocarbons through portions of tar sands formations with a fluid  

DOE Patents [OSTI]

A method for treating a tar sands formation is disclosed. The method includes heating a first portion of a hydrocarbon layer in the formation from one or more heaters located in the first portion. The heat is controlled to increase a fluid injectivity of the first portion. A drive fluid and/or an oxidizing fluid is injected and/or created in the first portion to cause at least some hydrocarbons to move from a second portion of the hydrocarbon layer to a third portion of the hydrocarbon layer. The second portion is between the first portion and the third portion. The first, second, and third portions are horizontally displaced from each other. The third portion is heated from one or more heaters located in the third portion. Hydrocarbons are produced from the third portion of the formation. The hydrocarbons include at least some hydrocarbons from the second portion of the formation.

Stegemeier, George Leo; Mudunuri, Ramesh Raju; Vinegar, Harold J.; Karanikas, John Michael; Jaiswal, Namit; Mo, Weijian

2010-05-18T23:59:59.000Z

445

Quantitative Changes in Hydrocarbons over Time in Fecal Pellets of Incisitermes minor May Predict Whether Colonies Are Alive or Dead  

E-Print Network [OSTI]

Food utilization and fecal pellet production by drywoodexploring seasonality in pellet production and hydrocarbon

Lewis, Vernard R.; Nelson, Lori J.; Haverty, Michael I.; Baldwin, James A.

2010-01-01T23:59:59.000Z

446

INTRODUCTION Asphalt is a mixture of a wide variety of chemical compounds that include aliphatic hydrocarbons and highly fused  

E-Print Network [OSTI]

hydrocarbons and highly fused aromatic ring systems.They are classified as asphaltenes (medium molecular weight

Harms, Kyle E.

447

Ozone-depleting-substance control and phase-out plan  

SciTech Connect (OSTI)

Title VI of the Federal Clean Air Act Amendments of 1990 requires regulation of the use and disposal of ozone-depleting substances (ODSs) (e.g., Halon, Freon). Several important federal regulations have been promulgated that affect the use of such substances at the Hanford Site. On April 23, 1993, Executive Order (EO) 12843, Procurement Requirements and Policies for Federal Agencies for Ozone-Depleting Substances (EPA 1993) was issued for Federal facilities to conform to the new US Environmental Protection Agency (EPA) regulations implementing the Clean Air Act of 1963 (CAA), Section 613, as amended. To implement the requirements of Title VI the US Department of Energy, Richland Operations Office (RL), issued a directive to the Hanford Site contractors on May 25, 1994 (Wisness 1994). The directive assigns Westinghouse Hanford Company (WHC) the lead in coordinating the development of a sitewide comprehensive implementation plan to be drafted by July 29, 1994 and completed by September 30, 1994. The implementation plan will address several areas where immediate compliance action is required. It will identify all current uses of ODSs and inventories, document the remaining useful life of equipment that contains ODS chemicals, provide a phase-out schedule, and provide a strategy that will be implemented consistently by all the Hanford Site contractors. This plan also addresses the critical and required elements of Federal regulations, the EO, and US Department of Energy (DOE) guidance. This plan is intended to establish a sitewide management system to address the clean air requirements.

Nickels, J.M.; Brown, M.J.

1994-07-01T23:59:59.000Z

448

INFLUENCE OF ELEVATED OZONE AND CARBON DIOXIDE ON INSECT DENSITIES.  

SciTech Connect (OSTI)

The combustion of fossil fuels is profoundly altering the chemical composition of the atmosphere. Beginning with the Industrial Revolution, the concentration of carbon dioxide in the atmosphere has increased from approximately 280 to 370 {micro}l l{sup -1} in 2004, and it is expected to exceed 550 {micro}l l{sup -1} by 2050. Tropospheric ozone has risen even more rapidly than CO{sub 2} and average summer concentrations in the Northern Hemisphere are expected to continue to increase by 0.5-2.5% per year over the next 30 years. Although elevated CO{sub 2} stimulates photosynthesis and productivity of terrestrial ecosystems, ozone (O{sub 3}) is deleterious. In addition to directly affecting the physiology and productivity of crops, increased concentrations of tropospheric CO{sub 2} and O{sub 3} are predicted to lower the nutritional quality of leaves, which has the potential to increase herbivory as insects eat more to meet their nutritional demands. We tested the hypothesis that changes in tropospheric chemistry affect the relationship between plants and insect herbivores by changing leaf quality. The susceptibility to herbivory of soybean grown in elevated CO{sub 2} or O{sub 3} was examined using free air gas concentration enrichment (SoyFACE). FACE technology has the advantage that plants are cultivated under realistic field conditions with no unwanted alteration of microclimate or artificial constraints on the insect community.

DELUCIA, E.; DERMODY, O.; O'NEILL, B.; ALDEA, M.; HAMILTON, J.; ZANGERL, A.; ROGER, A.; BERENBAUM, M.

2005-01-05T23:59:59.000Z

449

THE IMPACT OF OZONE ON THE LOWER FLAMMABLE LIMIT OF HYDROGEN IN VESSELS CONTAINING SAVANNAH RIVER SITE HIGH LEVEL WASTE  

SciTech Connect (OSTI)

The Savannah River Site, in conjunction with AREVA Federal services, has designed a process to treat dissolved radioactive waste solids with ozone. It is known that in this radioactive waste process, radionuclides radiolytically break down water into gaseous hydrogen and oxygen, which presents a well defined flammability hazard. Flammability limits have been established for both ozone and hydrogen separately; however, there is little information on mixtures of hydrogen and ozone. Therefore, testing was designed to provide critical flammability information necessary to support safety related considerations for the development of ozone treatment and potential scale-up to the commercial level. Since information was lacking on flammability issues at low levels of hydrogen and ozone, a testing program was developed to focus on filling this portion of the information gap. A 2-L vessel was used to conduct flammability tests at atmospheric pressure and temperature using a fuse wire ignition source at 1 percent ozone intervals spanning from no ozone to the Lower Flammable Limit (LFL) of ozone in the vessel, determined as 8.4%(v/v) ozone. An ozone generator and ozone detector were used to generate and measure the ozone concentration within the vessel in situ, since ozone decomposes rapidly on standing. The lower flammability limit of hydrogen in an ozone-oxygen mixture was found to decrease from the LFL of hydrogen in air, determined as 4.2 % (v/v) in this vessel. From the results of this testing, Savannah River was able to develop safety procedures and operating parameters to effectively minimize the formation of a flammable atmosphere.

Sherburne, Carol [Savannah River Site (SRS), Aiken, SC (United States). Savannah River Remediation, LLC; Osterberg, Paul [Fauske and Associates, LLC, Burr Ridge, IL (United States); Johnson, Tom [Fauske and Associates, LLC, Burr Ridge, IL (United States); Frawely, Thomas [Fauske and Associates, LLC, Burr Ridge, IL (United States)

2013-01-23T23:59:59.000Z

450

Plasma-induced conversion of surface-adsorbed hydrocarbons  

SciTech Connect (OSTI)

Experimental results are reported for an electrical device for direct conversion of methane into higher hydrocarbons. A microchannel plate is excited with electrons from a photoemissive source, and electron impact ionization of methane on the inner surfaces of the microchannels creates an ion feedback process. The resulting low-density plasma creates higher hydrocarbons when charged particles impact the surfaces at grazing incidence. The production Of C{sub 2} to C{sub 8}-containing gases was noted, with a selectivity for C{sub 2} of 39% in one case. The proportions of converted products and the conversion rates depend upon the electrical voltage, the microchannel geometry, and the operating pressure. Conversion rates increase with operating pressure.

Sackinger, W.M.

1992-07-01T23:59:59.000Z

451

Plasma-induced conversion of surface-adsorbed hydrocarbons  

SciTech Connect (OSTI)

Experimental results are reported for an electrical device for direct conversion of methane into higher hydrocarbons. A microchannel plate is excited with electrons from a photoemissive source, and electron impact ionization of methane on the inner surfaces of the microchannels creates an ion feedback process. The resulting low-density plasma creates higher hydrocarbons when charged particles impact the surfaces at grazing incidence. The production Of C{sub 2} to C{sub 8}-containing gases was noted, with a selectivity for C{sub 2} of 39% in one case. The proportions of converted products and the conversion rates depend upon the electrical voltage, the microchannel geometry, and the operating pressure. Conversion rates increase with operating pressure.

Sackinger, W.M.

1992-01-01T23:59:59.000Z

452

Biological Conversion of Sugars to Hydrocarbons Technology Pathway  

SciTech Connect (OSTI)

In support of the Bioenergy Technologies Office, the National Renewable Energy Laboratory (NREL) and the Pacific Northwest National Laboratory (PNNL) are undertaking studies of biomass conversion technologies to identify barriers and target research toward reducing conversion costs. Process designs and preliminary economic estimates for each of these pathway cases were developed using rigorous modeling tools (Aspen Plus and Chemcad). These analyses incorporated the best information available at the time of development, including data from recent pilot and bench-scale demonstrations, collaborative industrial and academic partners, and published literature and patents. This technology pathway case investigates the biological conversion of biomass derived sugars to hydrocarbon biofuels, utilizing data from recent literature references and information consistent with recent pilot scale demonstrations at NREL. Technical barriers and key research needs have been identified that should be pursued for the pathway to become competitive with petroleum-derived gasoline, diesel and jet range hydrocarbon blendstocks.

Davis, Ryan; Biddy, Mary J.; Tan, Eric; Tao, Ling; Jones, Susanne B.

2013-03-31T23:59:59.000Z

453

Estimating The Thermodynamics And Kinetics Of Chlorinated Hydrocarbon Degradation  

SciTech Connect (OSTI)

Many different degradation reactions of chlorinated hydrocarbons are possible in natural ground waters. In order to identify which degradation reactions are important, a large number of possible reaction pathways must be sorted out. Recent advances in ab initio electronic structure methods have the potential to help identify relevant environmental degradation reactions by characterizing the thermodynamic properties of all relevant contaminant species and intermediates for which experimental data is usually not available, as well as provide activation energies for relevant pathways. In this paper, strategies based on ab initio electronic structure methods for estimating thermochemical and kinetic properties of reactions with chlorinated hydrocarbons are presented. Particular emphasis is placed on strategies that are computationally fast and can be used for large organochlorine compounds such as 4,4?-DDT.

Bylaska, Eric J.

2006-08-01T23:59:59.000Z

454

Algal Lipid Extraction and Upgrading to Hydrocarbons Technology Pathway  

SciTech Connect (OSTI)

In support of the Bioenergy Technologies Office, the National Renewable Energy Laboratory (NREL) and the Pacific Northwest National Laboratory (PNNL) are undertaking studies of biomass conversion technologies to identify barriers and target research toward reducing conversion costs. Process designs and preliminary economic estimates for each of these pathway cases were developed using rigorous modeling tools (Aspen Plus and Chemcad). These analyses incorporated the best information available at the time of development, including data from recent pilot and bench-scale demonstrations, collaborative industrial and academic partners, and published literature and patents. This technology pathway case investigates the cultivation of algal biomass followed by further lipid extraction and upgrading to hydrocarbon biofuels. Technical barriers and key research needs have been assessed in order for the algal lipid extraction and upgrading pathway to be competitive with petroleum-derived gasoline, diesel and jet range hydrocarbon blendstocks.

Davis, Ryan; Biddy, Mary J.; Jones, Susanne B.

2013-03-31T23:59:59.000Z

455

Method for removing hydrocarbon contaminants from solid materials  

DOE Patents [OSTI]

A system for removing hydrocarbons from solid materials. Contaminated solids are combined with a solvent (preferably terpene based) to produce a mixture. The mixture is washed with water to generate a purified solid product (which is removed from the system) and a drainage product. The drainage product is separated into a first fraction (consisting mostly of contaminated solvent) and a second fraction (containing solids and water). The first fraction is separated into a third fraction (consisting mostly of contaminated solvent) and a fourth fraction (containing residual solids and water). The fourth fraction is combined with the second fraction to produce a sludge which is separated into a fifth fraction (containing water which is ultimately reused) and a sixth fraction (containing solids). The third fraction is then separated into a seventh fraction (consisting of recovered solvent which is ultimately reused) and an eighth fraction (containing hydrocarbon waste).

Bala, Gregory A. (Idaho Falls, ID); Thomas, Charles P. (Idaho Falls, ID)

1995-01-01T23:59:59.000Z

456

Apparatus for removing hydrocarbon contaminants from solid materials  

DOE Patents [OSTI]

A system for removing hydrocarbons from solid materials. Contaminated solids are combined with a solvent (preferably terpene based) to produce a mixture. The mixture is washed with water to generate a purified solid product (which is removed from the system) and a drainage product. The drainage product is separated into a first fraction (consisting mostly of contaminated solvent) and a second fraction (containing solids and water). The first fraction is separated into a third fraction (consisting mostly of contaminated solvent) and a fourth fraction (containing residual solids and water). The fourth fraction is combined with the second fraction to produce a sludge which is separated into a fifth fraction (containing water which is ultimately reused) and a sixth fraction (containing solids). The third fraction is then separated into a seventh fraction (consisting of recovered solvent which is ultimately reused) and an eighth fraction (containing hydrocarbon waste).

Bala, Gregory A. (Idaho Falls, ID); Thomas, Charles P. (Idaho Falls, ID)

1996-01-01T23:59:59.000Z

457

Process for partial oxidation of a hydrocarbon-containing fuel  

SciTech Connect (OSTI)

This patent describes a process for partial oxidation of a hydrocarbon-containing fuel comprising supplying an oxygen-containing gas and a hydrocarbon-containing fuel to a gasification zone through a concentric arrangement of three oxygen channels and one fuel channel, and oxidizing the fuel and producing auto-thermically a gaseous stream containing synthesis gas, the oxygen-containing gas being supplied through the central channel of the concentric arrangement at a velocity of 21-42 m/sec and through the first concentric channel encircling the central channel at a velocity of 60-120 m/sec, fuel being supplied through the second concentric channel encircling the first channel at a velocity of 3.0-3.8 m/sec, and oxygen-containing gas being supplied through the third concentric channel encircling the second channel at a velocity of 60-120 m/sec.

Martens, F.J.A.; Hasenack, H.J.A.

1988-12-06T23:59:59.000Z

458

Catalysts for conversion of methane to higher hydrocarbons  

DOE Patents [OSTI]

Catalysts for converting methane to higher hydrocarbons such as ethane and ethylene in the presence of oxygen at temperatures in the range of about 700.degree. to 900.degree. C. are described. These catalysts comprise calcium oxide or gadolinium oxide respectively promoted with about 0.025-0.4 mole and about 0.1-0.7 mole sodium pyrophosphate. A preferred reaction temperature in a range of about 800.degree. to 850.degree. C. with a preferred oxygen-to-methane ratio of about 2:1 provides an essentially constant C.sub.2 hydrocarbon yield in the range of about 12 to 19 percent over a period of time greater than about 20 hours.

Siriwardane, Ranjani V. (Morgantown, WV)

1993-01-01T23:59:59.000Z

459

Apparatus for removing hydrocarbon contaminants from solid materials  

DOE Patents [OSTI]

A system is described for removing hydrocarbons from solid materials. Contaminated solids are combined with a solvent (preferably terpene based) to produce a mixture. The mixture is washed with water to generate a purified solid product (which is removed from the system) and a drainage product. The drainage product is separated into a first fraction (consisting mostly of contaminated solvent) and a second fraction (containing solids and water). The first fraction is separated into a third fraction (consisting mostly of contaminated solvent) and a fourth fraction (containing residual solids and water). The fourth fraction is combined with the second fraction to produce a sludge which is separated into a fifth fraction (containing water which is ultimately reused) and a sixth fraction (containing solids). The third fraction is then separated into a seventh fraction (consisting of recovered solvent which is ultimately reused) and an eighth fraction (containing hydrocarbon waste). 4 figs.

Bala, G.A.; Thomas, C.P.

1996-02-13T23:59:59.000Z

460

Method for removing hydrocarbon contaminants from solid materials  

DOE Patents [OSTI]

A system is described for removing hydrocarbons from solid materials. Contaminated solids are combined with a solvent (preferably terpene based) to produce a mixture. The mixture is washed with water to generate a purified solid product (which is removed from the system) and a drainage product. The drainage product is separated into a first fraction (consisting mostly of contaminated solvent) and a second fraction (containing solids and water). The first fraction is separated into a third fraction (consisting mostly of contaminated solvent) and a fourth fraction (containing residual solids and water). The fourth fraction is combined with the second fraction to produce a sludge which is separated into a fifth fraction (containing water which is ultimately reused) and a sixth fraction (containing solids). The third fraction is then separated into a seventh fraction (consisting of recovered solvent which is ultimately reused) and an eighth fraction (containing hydrocarbon waste). 4 figs.

Bala, G.A.; Thomas, C.P.

1995-10-03T23:59:59.000Z

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

Surface modification of nitrogen-doped carbon nanotubes by ozone via atomic layer deposition  

SciTech Connect (OSTI)

The use of ozone as an oxidizing agent for atomic layer deposition (ALD) processes is rapidly growing due to its strong oxidizing capabilities. However, the effect of ozone on nanostructured substrates such as nitrogen-doped multiwalled carbon nanotubes (NCNTs) and pristine multiwalled carbon nanotubes (PCNTs) are not very well understood and may provide an avenue toward functionalizing the carbon nanotube surface prior to deposition. The effects of ALD ozone treatment on NCNTs and PCNTs using 10?wt. % ozone at temperatures of 150, 250, and 300?°C are studied. The effect of ozone pulse time and ALD cycle number on NCNTs and PCNTs was also investigated. Morphological changes to the substrate were observed by scanning electron microscopy and high resolution transmission electron microscopy. Brunauer-Emmett-Teller measurements were also conducted to determine surface area, pore size, and pore size distribution following ozone treatment. The graphitic nature of both NCNTs and PCNTs was determined using Raman analysis while x-ray photoelectron spectroscopy (XPS) was employed to probe the chemical nature of NCNTs. It was found that O{sub 3} attack occurs preferentially to the outermost geometric surface of NCNTs. Our research also revealed that the deleterious effects of ozone are found only on NCNTs while little or no damage occurs on PCNTs. Furthermore, XPS analysis indicated that ALD ozone treatment on NCNTs, at elevated temperatures, results in loss of nitrogen content. Our studies demonstrate that ALD ozone treatment is an effective avenue toward creating low nitrogen content, defect rich substrates for use in electrochemical applications and ALD of various metal/metal oxides.

Lushington, Andrew; Liu, Jian; Tang, Yongji; Li, Ruying; Sun, Xueliang, E-mail: xsun@eng.uwo.ca [Department of Mechanical and Materials Engineering, University of Western Ontario, London, Ontario N6A 5B9 (Canada)

2014-01-15T23:59:59.000Z

462

Preliminary investigation of the nature of hydrocarbon migration and entrapment  

E-Print Network [OSTI]

structures. The charge time for commercial hydrocarbon accumulation is much longer in oil-water systems than in oil-gas-water systems. Faults are classified into charging faults and ?back doors? ? faults other than charging faults in stacked fault...-bounded reservoirs. The lower the displacement pressure of a fault, the higher its updip oil transportation ability. The downdip oil transportation ability of a fault is usually low and cannot cause commercial downdip oil accumulation. Back doors affect both...

Bai, Jianyong

2004-09-30T23:59:59.000Z

463

Direct production of fractionated and upgraded hydrocarbon fuels from biomass  

SciTech Connect (OSTI)

Multistage processing of biomass to produce at least two separate fungible fuel streams, one dominated by gasoline boiling-point range liquids and the other by diesel boiling-point range liquids. The processing involves hydrotreating the biomass to produce a hydrotreatment product including a deoxygenated hydrocarbon product of gasoline and diesel boiling materials, followed by separating each of the gasoline and diesel boiling materials from the hydrotreatment product and each other.

Felix, Larry G.; Linck, Martin B.; Marker, Terry L.; Roberts, Michael J.

2014-08-26T23:59:59.000Z

464

Polycyclic aromatic hydrocarbon distributions in Mississippi Fan sediments  

E-Print Network [OSTI]

/ / / / / / glg. 4. Diag~am showing the morphology and lithologic bed associations of a submarine fan (adapted from IIANER, 1971). 16 indicative of land-sourced organic matter even in the intraslope basins. Furthermore, KENNICUTT et ai, (1986a) concluded.... Sandberg, B. A. , University of Colorado Chairman of Advisory Committee: Dr. James M. Brooks Polycyclic aromatic hydrocarbon (PAH) distributions in Upper Pleistocene sediments of the Mississippi Fan and two intraslope basins in the Gulf of Mexico...

Sandberg, William Allan

1986-01-01T23:59:59.000Z

465

Irregular spacing of heat sources for treating hydrocarbon containing formations  

DOE Patents [OSTI]

A method for treating a hydrocarbon containing formation includes providing heat input to a first section of the formation from one or more heat sources located in the first section. Fluids are produced from the first section through a production well located at or near the center of the first section. The heat sources are configured such that the average heat input per volume of formation in the first section increases with distance from the production well.

Miller, David Scott (Katy, TX); Uwechue, Uzo Philip (Houston, TX)

2012-06-12T23:59:59.000Z

466

THE INFRARED SPECTROSCOPY OF NEUTRAL POLYCYCLIC AROMATIC HYDROCARBON CLUSTERS  

SciTech Connect (OSTI)

The mid-infrared spectra of neutral homogeneous polycyclic aromatic hydrocarbon (PAH) clusters have been computed using density functional theory including an empirical correction for dispersion. The C-H out-of-plane bending modes are redshifted for all the clusters considered in this work. The magnitude of the redshift and the peak broadening are dependent on PAH size, shape, and on the PAH arrangement in the cluster.

Ricca, Alessandra [Carl Sagan Center, SETI Institute, 189 Bernardo Avenue, Suite 100, Mountain View, CA 94043 (United States); Bauschlicher, Charles W. Jr. [Entry Systems and Technology Division, Mail Stop 230-3, NASA Ames Research Center, Moffett Field, CA 94035 (United States); Allamandola, Louis J., E-mail: Alessandra.Ricca-1@nasa.gov, E-mail: Charles.W.Bauschlicher@nasa.gov [Space Science Division, Mail Stop 245-6, NASA Ames Research Center, Moffett Field, CA 94035 (United States)

2013-10-10T23:59:59.000Z

467

The Formation of Nitriles in Hydrocarbon-Rich Atmospheres  

E-Print Network [OSTI]

as the hydrocarbons ethane (C2H6), acetylene (C2H2), ethyl- ene (C2H4), methylacetylene (CH3CCH), propane (C3H8), methylacetylene (CH3CCH), propane (C3H8), and diacetylene (C4H2).3 Even though the above molecules. Nitriles can be hydrolyzed and react via multistep synthesis ultimately to amino acids, thus pro

Kaiser, Ralf I.

468

Method and apparatus for production of subsea hydrocarbon formations  

DOE Patents [OSTI]

A well tender system for controlling, separating, storing and offloading well fluids produced from subsea hydrocarbon formations. The system comprises a vertically aligned series of tethered cylindrical tanks which are torsionally stabilized by flexible catenary production riser and expert riser bundles, and serviced by separate catenary pipe bundles. Piles are secured to the seabed, each pile assembly being pivotally connected to a lower rigid tendon, which is in turn connected to tendons arranged about the periphery of the interconnected cylindrical tanks.

Blandford, Joseph W. (15 Mott La., Houston, TX 77024)

1992-01-01T23:59:59.000Z

469

Method and apparatus for production of subsea hydrocarbon formations  

DOE Patents [OSTI]

A well tender system for controlling, separating, storing and offloading well fluids produced from subsea hydrocarbon formations. The system comprises a vertically aligned series of tethered cylindrical tanks which are torsionally stabilized by flexible catenary production riser and export riser bundles, and serviced by separate catenary pipe bundles. Piles are secured to the seabed, each pile assembly being pivotally connected to a lower rigid tendon, which is in turn connected to tendons arranged about the periphery of the interconnected cylindrical tanks.

Blandford, Joseph W. (15 Mott La., Houston, TX 77024)

1994-01-01T23:59:59.000Z

470

Production of valuable hydrocarbons by flash pyrolysis of oil shale  

DOE Patents [OSTI]

A process for the production of gas and liquid hydrocarbons from particulated oil shale by reaction with a pyrolysis gas at a temperature of from about 700/sup 0/C to about 1100/sup 0/C, at a pressure of from about 400 psi to about 600 psi, for a period of about 0.2 second to about 20 seconds. Such a pyrolysis gas includes methane, helium, or hydrogen. 3 figs., 3 tabs.

Steinberg, M.; Fallon, P.T.

1985-04-01T23:59:59.000Z

471

Aerobic microorganism for the degradation of chlorinated aliphatic hydrocarbons  

DOE Patents [OSTI]

A chlorinated aliphatic hydrocarbon-degrading microorganism, having American Type Culture Collection accession numbers ATCC 53570 and 53571, in a biologically pure culture aseptically collected from a deep subsurface habitat and enhanced, mineralizes trichloroethylene and tetrachloroethylene to HCl, H.sub.2 O and Co.sub.2 under aerobic conditions stimulated by methane, acetate, methanol, tryptone-yeast extract, propane and propane-methane.

Fliermans, Carl B. (Augusta, GA)

1989-01-01T23:59:59.000Z

472

Thermocatalytic CO2-Free Production of Hydrogen from Hydrocarbon Fuels  

SciTech Connect (OSTI)

The main objective of this project is the development of an economically viable thermocatalytic process for production of hydrogen and carbon from natural gas or other hydrocarbon fuels with minimal environmental impact. The three major technical goals of this project are: (1) to accomplish efficient production of hydrogen and carbon via sustainable catalytic decomposition of methane or other hydrocarbons using inexpensive and durable carbon catalysts, (2) to obviate the concurrent production of CO/CO{sub 2} byproducts and drastically reduce CO{sub 2} emissions from the process, and (3) to produce valuable carbon products in order to reduce the cost of hydrogen production The important feature of the process is that the reaction is catalyzed by carbon particulates produced in the process, so no external catalyst is required (except for the start-up operation). This results in the following advantages: (1) no CO/CO{sub 2} byproducts are generated during hydrocarbon decomposition stage, (2) no expensive catalysts are used in the process, (3) several valuable forms of carbon can be produced in the process depending on the process conditions (e.g., turbostratic carbon, pyrolytic graphite, spherical carbon particles, carbon filaments etc.), and (4) CO{sub 2} emissions could be drastically reduced (compared to conventional processes).

University of Central Florida

2004-01-30T23:59:59.000Z

473

Hydrocarbon reforming catalyst material and configuration of the same  

DOE Patents [OSTI]

A hydrocarbon reforming catalyst material comprising a catalyst support impregnated with catalyst is provided for reforming hydrocarbon fuel gases in an electrochemical generator. Elongated electrochemical cells convert the fuel to electrical power in the presence of an oxidant, after which the spent fuel is recirculated and combined with a fresh hydrocarbon feed fuel forming the reformable gas mixture which is fed to a reforming chamber containing a reforming catalyst material, where the reforming catalyst material includes discrete passageways integrally formed along the length of the catalyst support in the direction of reformable gas flow. The spent fuel and/or combusted exhaust gases discharged from the generator chamber transfer heat to the catalyst support, which in turn transfers heat to the reformable gas and to the catalyst, preferably via a number of discrete passageways disposed adjacent one another in the reforming catalyst support. The passageways can be slots extending inwardly from an outer surface of the support body, which slots are partly defined by an exterior confining wall. According to a preferred embodiment, the catalyst support is non-rigid, porous, fibrous alumina, wherein the fibers are substantially unsintered and compressible, and the reforming catalyst support is impregnated, at least in the discrete passageways with Ni and MgO, and has a number of internal slot passageways for reformable gas, the slot passageways being partly closed by a containing outer wall.

Singh, Prabhakar (Export, PA); Shockling, Larry A. (Plum Borough, PA); George, Raymond A. (Pittsburgh, PA); Basel, Richard A. (Plub Borough, PA)

1996-01-01T23:59:59.000Z

474

Federal Environmental Regulations Impacting Hydrocarbon Exploration, Drilling, and Production Operations  

SciTech Connect (OSTI)

Waste handling and disposal from hydrocarbon exploration, drilling, and production are regulated by the US Environmental Protection Agency (EPA) through federal and state regulations and/or through implementation of federal regulations. Some wastes generated in these operations are exempt under the Resource Conservation and Recovery Act (RCRA) but are not exempt under the Comprehensive Environmental Response, Compensation, and Liability Act (CERCLA), Superfund Amendments and Reauthorization Act (SARA), and other federal environmental laws. Exempt wastes remain exempt only if they are not mixed with hazardous wastes or hazardous substances. Once mixture occurs, the waste must be disposed as a hazardous material in an approved hazardous waste disposal facility. Before the Clean Air Act as amended in 1990, air emissions from production, storage, steam generation, and compression facilities associated with hydrocarbon exploration, drilling, and production industry were not regulated. A critical proposed regulatory change which will significantly effect Class II injection wells for disposal of produced brine and injection for enhanced oil recovery is imminent. Federal regulations affecting hydrocarbon exploration, drilling and production, proposed EPA regulatory changes, and a recent significant US Court of Appeals decision are covered in this report. It appears that this industry will, in the future, fall under more stringent environmental regulations leading to increased costs for operators.

Carroll, Herbert B.; Johnson, William I.

1999-04-27T23:59:59.000Z

475

Paleotopography and hydrocarbon accumulation: Williston, Powder River, and Denver basins  

SciTech Connect (OSTI)

Recent geomorphic analyses of 1:24,000 scale topographic maps in the three major basins of the northern Great Plains have disclosed a persistent system of basement paleotopographic features that trend north-northeast throughout the region. Superimposed across this system and subtly influenced by it, are the northwesterly trending Laramide structural features. Paleozoic depositional patterns have been strongly influenced by the paleoridge and trough system formed by the north-northeast features. Mesozoic deposition has also been affected by the ancient subsurface system but in a more subtle manner. Many of the Paleozoic and Mezoxoic hydrocarbon locations in the three basins appear to be the results of paleotopographic control on hydrocarbon accumulation sites. This affect ranges from Paleozoic reef sites in the Williston basin through paleotrough localization of Pennsylvanian Minnelusa production in the Powder River basin to fractured Cretaceous Niobrara production at the Silo field in the Denver basin. Basement paleotopography is the underlying factor in all deposition and subsequent hydrocarbon migration in any basin. As such, it should be considered a major factor in the exploration for oil and gas.

Thomas, G.E. (Thomas and Associates, Denver, CO (United States))

1991-06-01T23:59:59.000Z

476

Hydrocarbon reforming catalyst material and configuration of the same  

DOE Patents [OSTI]

A hydrocarbon reforming catalyst material comprising a catalyst support impregnated with catalyst is provided for reforming hydrocarbon fuel gases in an electrochemical generator. Elongated electrochemical cells convert the fuel to electrical power in the presence of an oxidant, after which the spent fuel is recirculated and combined with a fresh hydrocarbon feed fuel forming the reformable gas mixture which is fed to a reforming chamber containing a reforming catalyst material, where the reforming catalyst material includes discrete passageways integrally formed along the length of the catalyst support in the direction of reformable gas flow. The spent fuel and/or combusted exhaust gases discharged from the generator chamber transfer heat to the catalyst support, which in turn transfers heat to the reformable gas and to the catalyst, preferably via a number of discrete passageways disposed adjacent one another in the reforming catalyst support. The passageways can be slots extending inwardly from an outer surface of the support body, which slots are partly defined by an exterior confining wall. According to a preferred embodiment, the catalyst support is non-rigid, porous, fibrous alumina, wherein the fibers are substantially unsintered and compressible, and the reforming catalyst support is impregnated, at least in the discrete passageways with Ni and MgO, and has a number of internal slot passageways for reformable gas, the slot passageways being partly closed by a containing outer wall. 5 figs.

Singh, P.; Shockling, L.A.; George, R.A.; Basel, R.A.

1996-06-18T23:59:59.000Z

477

Oxidation of methyl tert-butyl ether (MTBE) and ethyl tert-butyl ether (ETBE) by ozone and combined ozone/hydrogen peroxide  

SciTech Connect (OSTI)

The aim of this work was to study the reaction of ozone and combined ozone/hydrogen peroxide on oxygenated additives such as methyl tert-butyl ether (MTBE) and ethyl tert-butyl ether (ETBE) in dilute aqueous solution using controlled experimental conditions. Experiments conducted in a semi-continuous reactor with MTBE and ETBE in combination (initial concentration: 2 mmol/L of each) showed that ETBE was better eliminated than MTBE with both ozone and combined O[sub 3]/H[sub 2]O[sub 2]. batch experiments led to the determination of the ratio of the kinetic constants for the reaction of OH[degree]-radical with MTBE and ETBE (k[sub OH[degree]/ETBE]/k[sub OH[degree]//MTBE] = 1.7). Tert-butyl formate and tert-butyl acetate were identified as the ozonation byproducts of MTBE an ETBE, respectively, while tert-butyl alcohol was found to be produced during the ozonation of both compounds. 10 refs., 10 figs., 1 tab.

Leitner, N.K.V.; Papailhou, A.L.; Croue, J.P.; Dore, M. (Univ. de Poitiers (France)); Peyrot, J. (British Petroleum, Harfleur (France))

1994-01-01T23:59:59.000Z

478

Scale-Up and Demonstration of Fly Ash Ozonation Technology  

SciTech Connect (OSTI)

This is the fourth quarterly report under DOE Cooperative Agreement No.: DE-FC26-03NT41730. Due a number of circumstances, mostly associated with subcontractor agreements, the actual beginning of the project was delayed from its original award date of March 5, 2003. DOE's Project Manager was kept informed (verbally) by PPL's Project Manager throughout this period. Because of this delay, this is the fourth quarterly report and it refers to the time period from January to March 2004. The on-site deployment and testing of the ozonation system took place during this period. This report summarizes these activities including some preliminary results. No significant issues or concerns are identified.

Larry LaBuz; Rui Afonso

2005-03-31T23:59:59.000Z

479

Method and apparatus for monitoring a hydrocarbon-selective catalytic reduction device  

DOE Patents [OSTI]

A method for monitoring a hydrocarbon-selective catalytic reactor device of an exhaust aftertreatment system of an internal combustion engine operating lean of stoichiometry includes injecting a reductant into an exhaust gas feedstream upstream of the hydrocarbon-selective catalytic reactor device at a predetermined mass flowrate of the reductant, and determining a space velocity associated with a predetermined forward portion of the hydrocarbon-selective catalytic reactor device. When the space velocity exceeds a predetermined threshold space velocity, a temperature differential across the predetermined forward portion of the hydrocarbon-selective catalytic reactor device is determined, and a threshold temperature as a function of the space velocity and the mass flowrate of the reductant is determined. If the temperature differential across the predetermined forward portion of the hydrocarbon-selective catalytic reactor device is below the threshold temperature, operation of the engine is controlled to regenerate the hydrocarbon-selective catalytic reactor device.

Schmieg, Steven J; Viola, Michael B; Cheng, Shi-Wai S; Mulawa, Patricia A; Hilden, David L; Sloane, Thompson M; Lee, Jong H

2014-05-06T23:59:59.000Z

480

Three-dimensional simulations of wintertime ozone variability in the lower stratosphere  

SciTech Connect (OSTI)

The evolution of ozone has been calculated for the winters of 1979 and 1989 using winds derived from the authors stratospheric data assimilation system (STRATAN). The ozone fields calculated using this technique are found to compare well with satellite-measured fields for simulations of 2-3 months. Here the authors present comparisons of model fields with both satellite and sonde measurements to verify that stratospheric transport processes are properly represented by this modeling technique. Attention is focussed on the northern hemisphere middle and high latitudes at the 10-hPa level and below, where transport processes are most important to the ozone distribution. First-order quantities and derived budgets from both the model and satellite data are presented. By sampling the model with a limb-viewing satellite and then Kalman filtering the observations of the model, it is shown that transient subplanetary-scale features that are essential to the ozone budget are missed by the satellite system.

Rood, R.B.; Douglass, A.R.; Kaye, J.A. (NASA Goddard Space Flight Center, Greenbelt, MD (USA)); Geller, M.A.; Yuechen, Chi (State Univ. of New York, Stony Brook (USA)); Allen, D.J.; Larson, E.M.; Nash, E.R.; Nielsen, J.E. (Applied Research Corp., Landover, MD (USA))

1991-03-20T23:59:59.000Z

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" 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

Climatology and Trends in the Forcing of the Stratospheric Ozone Transport  

E-Print Network [OSTI]

A thorough analysis of the ozone transport was carried out using the Transformed-Mean Eulerian (TEM) tracer transport equation and the European Centre for Medium-Range Weather Forecasts (ECMWF) Re- Analysis (ERA-40). In ...

Monier, Erwan

482

A Spatial Econometric Approach to Measuring Pollution Externalities: An Application to Ozone Smog  

E-Print Network [OSTI]

A Spatial Econometric Approach to Measuring Pollution Externalities: An Application to Ozone Smog C.-Y. Cynthia Lin University of California at Davis ­ USA Abstract. This paper uses spatial econometrics

Lin, C.-Y. Cynthia

483

Evaluation of a novel ozone generation technique for disinfection of poultry hatchers and processed broiler carcasses  

E-Print Network [OSTI]

When comparing electrochemically generated ozone(03)(2.94.2 wt % inside the (hatcher) and formaldehyde (16 n-A formalin + 7.5 g potassium pertnanganate) for disinfection of Salmonella enteiltidis (SE) contaminated agar plates and typical hatchery...

Ramirez, Gerardo Arturo

1994-01-01T23:59:59.000Z

484

Climatology and trends in the forcing of the stratospheric ozone transport  

E-Print Network [OSTI]

A thorough analysis of the ozone transport was carried out using the Transformed-Mean Eulerian (TEM) tracer continuity equation and the European Centre for Medium-Range Weather Forecasts (ECMWF) Re-Analysis (ERA-40). In ...

Monier, Erwan

485

Atmospheric Environment 39 (2005) 28292838 Diurnal and seasonal cycles of ozone precursors observed from  

E-Print Network [OSTI]

characteristics. Ethane and propane, largely originated from leakage of natural gas or liquefied petroleum gases) and nitrogen oxides (NO+NO2 ¼ NOx), ozone is photochemically pro- duced and can accumulate to hazardous levels

Wingenter, Oliver W.

486

Ozone response to emission changes: a modeling study during the MCMA-2006/MILAGRO Campaign  

E-Print Network [OSTI]

The sensitivity of ozone production to precursor emissions was investigated under five different meteorological conditions in the Mexico City Metropolitan Area (MCMA) during the MCMA-2006/MILAGRO field campaign using the ...

Song, Jihee

487

Real-World Studies of Ambient Ozone Formation as a Function of...  

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

-- Washington D.C. ace29lawson.pdf More Documents & Publications Weekday and Weekend Air Pollutant Levels in Ozone Problem Areas in the U.S. Health Impacts Program DOE's...

488

Ozone predictabilities due to meteorological uncertainties in the Mexico City basin using ensemble forecasts  

E-Print Network [OSTI]

The purpose of the present study is to investigate the sensitivity of ozone (O3)[(O subscript 3)] predictions in the Mexico City Metropolitan Area (MCMA) to meteorological initial uncertainties and planetary boundary layer ...

Bei, Naifang

489

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

490

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

491

Apparatus and method for rapid separation and detection of hydrocarbon fractions in a fluid stream  

DOE Patents [OSTI]

An apparatus and method for rapid fractionation of hydrocarbon phases in a sample fluid stream are disclosed. Examples of the disclosed apparatus and method include an assembly of elements in fluid communication with one another including one or more valves and at least one sorbent chamber for removing certain classifications of hydrocarbons and detecting the remaining fractions using a detector. The respective ratios of hydrocarbons are determined by comparison with a non separated fluid stream.

Sluder, Charles S.; Storey, John M.; Lewis, Sr., Samuel A.

2013-01-22T23:59:59.000Z

492

A study of the structure of the hydrocarbons of primary hard-coal tar  

SciTech Connect (OSTI)

The hydrocarbons isolated from primary hard-coal (G/sub 6/ gas coal) tar have been investigated by a combination of physicochemical and chemical methods. It has been established that the hydrocarbons boiling up to 573 K are mainly aliphatic, hydroaromatic, and naphthenic and are aromatic only to a smaller degree. Molecular and presumable structural formulas of the oxygen compounds isolated from the 473-573 K hydrocarbon fraction have been derived.

Platonov, V.V.; Gerasimova, N.I.; Ivleva, L.N.; Klyavina, O.A.; Vishnyakov, S.N.

1985-01-01T23:59:59.000Z

493

Formation of ozone and oxidation of methane in a direct current corona discharge  

E-Print Network [OSTI]

FORMATION OF OZONE AND OXIDATION OF METHANE IN A DIRECT CURRENT CORONA DISCHARGE A Thesis by UMASHANKER TANGIRALA Submitted to the Graduate College of Texas A&M University in partial fulfillment of the requirement for the degree of MASTER... OF SCIENCE May 1976 Major Subject: Chemical Engineering FORMATION OF OZONE AND OXIDATION OF METHANE IN A DIRECT CURRENT CORONA DISCHARGE A Thesis by UMASHANKER TANGIRALA Approved as to style and content by: (Chairman of Committee) ( ad of Department...

Tangirala, Umashanker

1976-01-01T23:59:59.000Z

494

E-Print Network 3.0 - aromatic hydrocarbons part Sample Search...  

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

By Abbas Firoozabadi Reservoir Engineering... Research Institute (RERI), Palo Alto Yale University, New Haven New phase formation is an integral part... of hydrocarbon...

495

E-Print Network 3.0 - adsorption equilibria hydrocarbons Sample...  

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

of water vapor and hydrocarbons by activated carbon beds: thermo- dynamic model for adsorption... of binary adsorption equilibria of solvent and water vapor on acti- Z .vated...

496

E-Print Network 3.0 - aromatic hydrocarbons adducted Sample Search...  

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

hydrocarbon... to its high reactivity toward DNA and cellular proteins. The major acrolein-DNA adduct, -hydrox- ypropano... -hy- droxynonenal, and acrolein, that readily form...

497

E-Print Network 3.0 - aliphatic hydrocarbons formed Sample Search...  

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

4.3. Lack of Aliphatic Hydrocarbons... might be interpreted as the results of contamination that introduced ... Source: Brocks, Jochen J. - Research School of Earth Sciences,...

498

E-Print Network 3.0 - aromatic hydrocarbon neutrals Sample Search...  

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

RANDHIR S. MAKKAR and KARL J. ROCKNE... --Polycyclic aromatic hydrocarbon (PAH) contamination of the environment represents a serious threat to the health... bioremediation...

499

E-Print Network 3.0 - aromatic hydrocarbon pah-degrading Sample...  

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

degradation Summary: Removal of polycyclic aromatic hydrocarbons (PAHs) from sewage sludge by anaerobic degradation N... , terminate in the sludge, and can be released to the...

500

E-Print Network 3.0 - abundant accessible hydrocarbons Sample...  

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

Functionalization: An Energy Frontier Research... such as hydrocarbons, dioxygen, water, carbon dioxide and dihydrogen are central to new technologies for the use... of...