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


1

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

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

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

2

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

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

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

3

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

SciTech Connect

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

Atherton, C.S.

1995-11-01T23:59:59.000Z

4

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

5

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

6

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

7

Ozone  

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

and Umkehr observations (Angell et al.) The Forest Responses to Anthropogenic Stress (FORAST) (McLaughlin et al.) Ozone EnrichmentAspen FACE Experiment - Rhinelander, Wisconsin...

8

Ozone  

SciTech Connect

The author discusses the debate over whether concern about a hole in the ozone layer in Antarctic is real or science fiction. There is a growing consensus that efforts must be taken to protect the ozone layer. The issue now is not whether chlorofluorocarbons (CFCs) should be controlled and regulated but how much and how soon. The United States has urged that the production of dangerous CFCs, and any other chemicals that affect the ozone layer, be restricted immediately to current levels and that their use be reduced 95 percent over the next decade. The American position was too strong for many European nations and the Japanese. Negotiations at an international conference on the matter broke down. The breakdown is due in part to a more acute concern for environmental matters in the United States than exists in many countries. Meanwhile CFCs are linked to another environmental problem that equally threatens the world - the Greenhouse Effect. The earth is in a natural warming period, but man could be causing it to become even warmer. The Greenhouse Effect could have a catastrophic impact on mankind, although nothing has been proven yet.

1988-06-01T23:59:59.000Z

9

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

10

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

Science Conference Proceedings (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

11

Large Scale Atmospheric Chemistry Simulations for 2001: An Analysis of Ozone and Other Species in Central Arizona  

DOE Green Energy (OSTI)

A key atmospheric gas is ozone. Ozone in the stratosphere is beneficial to the biosphere because it absorbs a significant fraction of the sun's shorter wavelength ultraviolet radiation. Ozone in the troposphere is a pollutant (respiratory irritant in humans and acts to damage crops, vegetation, and many materials). It affects the Earths energy balance by absorbing both incoming solar radiation and outgoing long wave radiation. An important part of the oxidizing capacity of the atmosphere involves ozone, through a photolysis pathway that leads to the hydroxyl radical (OH). Since reaction with OH is a major sink of many atmospheric species, its concentration controls the distributions of many radiatively important species. Ozone in the troposphere arises from both in-situ photochemical production and transport from the stratosphere. Within the troposphere, ozone is formed in-situ when carbon monoxide (CO), methane (CH4), and non-methane hydrocarbons (NMHCs) react in the presence of nitrogen oxides (NO, = NO + NO2) and sunlight. The photochemistry of the stratosphere differs significantly from that in the troposphere. Within the stratosphere, ozone formation is initiated by the photolysis of 02. Stratospheric ozone may be destroyed via catalytic reactions with NO, H (hydrogen), OH, CI (chlorine) and Br (bromine), or photolysis. In the past, attempts to simulate the observed distributions of ozone (and other important gases) have focused on either the stratosphere or the troposphere. Stratospheric models either employed simplified parameterizations to represent tropospheric chemical and physical processes, or assumed the troposphere behaved as a boundary condition. Likewise, tropospheric models used simplified stratospheric chemistry and transport.

Atherton, C; Bergmann, D; Cameron-Smith, P; Connell, P; Molenkamp, C; Rotman, D; Tannahil, J

2002-10-08T23:59:59.000Z

12

Analysis of the behavior of ternary hydrocarbon mixture as substitutes of the CFC-12  

Science Conference Proceedings (OSTI)

Hydrocarbons are stratospheric ozone friendly and have good heat transfer properties. The use of hydrocarbons (HCs) or their blend as refrigerant is extending in these days. This paper deals with the search of the best ternary hydrocarbons mixture of ... Keywords: CFC-12, LB-12, cub, hydrocarbon, ozone, refrigerant, ternary mixture

Rafael Quintero Ricardo

2007-05-01T23:59:59.000Z

13

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

E-Print Network (OSTI)

A microcomputer-based control system utilizing a distributed intelligence architecture has been developed to control combustion in hydrocarbon fuel-fired boilers and heaters to significantly reduce fuel usage. The system incorporates a unique flue 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 air fuel ratio control based on carbon monoxide measurements. Significant decreases in excess air result in reduced fuel usage while meeting steam demand. Actual performance on industrial boilers shows increases in efficiency of from 1% to 3% with substantial fuel savings.

DeVivo, D. G.

1980-01-01T23:59:59.000Z

14

Transient PrOx carbon monoxide measurement, control, and optimization  

DOE Green Energy (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

15

Carbon Monoxide Tolerant Electrocatalyst with Low Platinum ...  

Carbon Monoxide Tolerant Electrocatalyst with Low Platinum Loading and a Process for its Preparation Brookhaven National Laboratory. Contact BNL About ...

16

Numerical Simulation of Polycyclic Aromatic Hydrocarbon Formation in n-Heptane HCCI Combustion  

Science Conference Proceedings (OSTI)

By modifying the SENKIN code of CHEMKIN chemical kinetics package, the combustion processes and the characteristics of hydrocarbon (HC) and carbon monoxide(CO) emissions of a HCCI engine were simulated. Furthermore, the formation of benzene (A1) and ... Keywords: n-neptane, HCCI, multi-zone model, polycyclic aromatic hydrocarbons

Zeng Wen; Ma Hong-an

2011-02-01T23:59:59.000Z

17

Method of removing carbon monoxide from gases  

DOE Patents (OSTI)

A process and catalyst are disclosed for purifying an atmosphere containing carbon monoxide by passing the atmosphere through a bed of a catalyst of TbO.sub.x, where x = 1.8 to 1.5, which oxidizes the carbon monoxide to carbon dioxide.

Gerstein, Bernard C. (Ames, IA); Macaulay, David B. (Arlington Heights, IL)

1976-06-01T23:59:59.000Z

18

Why sequence carbon monoxide oxidizing thermophiles?  

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

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

19

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

20

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

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

Device for staged carbon monoxide oxidation  

DOE Patents (OSTI)

A method and apparatus for selectively oxidizing carbon monoxide in a hydrogen rich feed stream. The method comprises mixing a feed stream consisting essentially of hydrogen, carbon dioxide, water and carbon monoxide with a first predetermined quantity of oxygen (air). The temperature of the mixed feed/oxygen stream is adjusted in a first the heat exchanger assembly (20) to a first temperature. The mixed feed/oxygen stream is sent to reaction chambers (30,32) having an oxidation catalyst contained therein. The carbon monoxide of the feed stream preferentially absorbs on the catalyst at the first temperature to react with the oxygen in the chambers (30,32) with minimal simultaneous reaction of the hydrogen to form an intermediate hydrogen rich process stream having a lower carbon monoxide content than the feed stream. The elevated outlet temperature of the process stream is carefully controlled in a second heat exchanger assembly (42) to a second temperature above the first temperature. The process stream is then mixed with a second predetermined quantity of oxygen (air). The carbon monoxide of the process stream preferentially reacts with the second quantity of oxygen in a second stage reaction chamber (56) with minimal simultaneous reaction of the hydrogen in the process stream. The reaction produces a hydrogen rich product stream having a lower carbon monoxide content than the process stream. The product stream is then cooled in a third heat exchanger assembly (72) to a third predetermined temperature. Three or more stages may be desirable, each with metered oxygen injection.

Vanderborgh, Nicholas E. (Los Alamos, NM); Nguyen, Trung V. (College Station, TX); Guante, Jr., Joseph (Denver, CO)

1993-01-01T23:59:59.000Z

22

: Plasma-Hydrocarbon conversion  

crude oil and hydrocarbon gases like natural gas, into lighter hydrocarbon materials (e.g. synthetic light oil).

23

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

24

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

SciTech Connect

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

25

Hydrocarbon synthesis catalyst and method of preparation  

DOE Patents (OSTI)

A catalyst for the synthesis of hydrocarbons from carbon monoxide and hydrogen composed of palladium or platinum and cobalt supported on a solid phase is disclosed. The catalyst is prepared by heating a heterogeneous component of the palladium or platinum deposited on the solid support in a solution of cobalt carbonyl or precursors thereof. The catalyst exhibits excellent activity, stability in air, and produces highly desirable product fractions even with dilute gaseous reactants. The catalyst is preferably used in dilute slurry form, which is desirable from a heat transfer standpoint.

Sapienza, Richard S. (Shoreham, NY); Sansone, Michael J. (Summit, NJ); Slegeir, William A. R. (Hampton Bays, NY)

1983-08-02T23:59:59.000Z

26

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

27

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

28

Method and apparatus for selective removal of carbon monoxide  

DOE Patents (OSTI)

There is provided a method and apparatus for treatment of a hydrogen-rich gas to reduce the carbon monoxide content thereof by reacting the carbon monoxide in the gas with an amount of oxygen sufficient to oxidize at least a portion of the carbon monoxide in the presence of a catalyst in a desired temperature range without substantial reaction of hydrogen. The catalyst is an iridium-based catalyst dispersed on, and supported on, a carrier. In the presence of the catalyst, carbon monoxide in a hydrogen-rich feed gas is selectively oxidized such that a product stream is produced with a very low carbon monoxide content.

Borup, Rodney L. (East Rochester, NY); Skala, Glenn W. (Churchville, NY); Brundage, Mark A. (Pittsford, NY); LaBarge, William J. (Bay City, MI)

2000-01-01T23:59:59.000Z

29

Removing the Hydrocarbon from Hydrocarbon Flow ...  

Science Conference Proceedings (OSTI)

... gas and petroleum products. Therefore is important to have primary calibration standards with low uncertainty. NIST has several hydrocarbon liquid ...

2014-01-03T23:59:59.000Z

30

Carbon Monoxide in type II supernovae  

E-Print Network (OSTI)

Infrared spectra of two type II supernovae 6 months after explosion are presented. The spectra exhibit a strong similarity to the observations of SN 1987A and other type II SNe at comparable epochs. The continuum can be fitted with a cool black body and the hydrogen lines have emissivities that are approximately those of a Case B recombination spectrum. The data extend far enough into the thermal region to detect emission by the first overtone of carbon monoxide. The molecular emission is modeled and compared with that in the spectra of SN 1987A. It is found that the flux in the CO first overtone is comparable to that found in SN 1987A. We argue that Carbon Monoxide forms in the ejecta of all type II SNe during the first year after explosion.

J. Spyromilio; B. Leibundgut; R. Gilmozzi

2001-07-16T23:59:59.000Z

31

Enhanced carbon monoxide utilization in methanation process  

DOE Green Energy (OSTI)

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

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

1984-01-01T23:59:59.000Z

32

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

Science Conference Proceedings (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

33

Ozone in Michigan's Environment 1876–1880  

Science Conference Proceedings (OSTI)

Atmospheric ozone was monitored in Michigan during the late 1880's using Schoenbein's test paper. A conversion chart was constructed to relate the Schoenbein ozone scale at various relative humidifies to ozone levels indicated by a Dasibi ozone ...

Dale E. Linvill; W. J. Hooker; Brian Olson

1980-11-01T23:59:59.000Z

34

CO (Carbon Monoxide Mixing Ratio System) Handbook  

Science Conference Proceedings (OSTI)

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

Biraud, S

2011-02-23T23:59:59.000Z

35

Radiation and Ozone  

Science Conference Proceedings (OSTI)

Radiation is the driving force for the general circulation of the atmosphere and controls the Earth's climate. Ozone is responsible for the warm stratosphere and protects life on Earth from harmful solar ultraviolet radiation. In July 1959, the ...

G. Ohring; R. D. Bojkov; H-J. Bolle; R. D. Hudson; H. Volkert

2009-11-01T23:59:59.000Z

36

Search of medical literature for indoor carbon monoxide exposure  

SciTech Connect

This report documents a literature search on carbon monoxide. The search was limited to the medical and toxicological databases at the National Library of Medicine (MEDLARS). The databases searched were Medline, Toxline and TOXNET. Searches were performed using a variety of strategies. Combinations of the following keywords were used: carbon, monoxide, accidental, residential, occult, diagnosis, misdiagnosis, heating, furnace, and indoor. The literature was searched from 1966 to the present. Over 1000 references were identified and summarized using the following abbreviations: The major findings of the search are: (1) Acute and subacute carbon monoxide exposures result in a large number of symptoms affecting the brain, kidneys, respiratory system, retina, and motor functions. (2) Acute and subacute carbon monoxide (CO) poisonings have been misdiagnosed on many occasions. (3) Very few systematic investigations have been made into the frequency and consequences of carbon monoxide poisonings.

Brennan, T.; Ivanovich, M.

1995-12-01T23:59:59.000Z

37

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); Non-methane hydrocarbons (NMHCs); Liquefied petroleum gases (LPG); Temperature inversion ARTICLE) and nitrogen oxides (NO+NO2 ¼ NOx), ozone is photochemically pro- duced and can accumulate to hazardous levels

Wingenter, Oliver W.

38

Ozone Modeling Using Neural Networks  

Science Conference Proceedings (OSTI)

Ozone models for the city of Tulsa were developed using neural network modeling techniques. The neural models were developed using meteorological data from the Oklahoma Mesonet and ozone, nitric oxide, and nitrogen dioxide (NO2) data from ...

Ramesh Narasimhan; Joleen Keller; Ganesh Subramaniam; Eric Raasch; Brandon Croley; Kathleen Duncan; William T. Potter

2000-03-01T23:59:59.000Z

39

Observations of Transport Processes for Ozone and Ozone Precursors during the 1991 Lake Michigan Ozone Study  

Science Conference Proceedings (OSTI)

The Lake Michigan Air Quality Region (LMAQR) continues to experience ozone concentrations in urban and rural areas above the federal standard of 125 ppb. During the summer of 1991, the LMAQR states sponsored the Lake Michigan Ozone Study, which ...

Timothy S. Dye; Paul T. Roberts; Marcelo E. Korc

1995-08-01T23:59:59.000Z

40

Reduction of Carbon Monoxide. Past Research Summary  

DOE R&D Accomplishments (OSTI)

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

Schrock, R. R.

1982-00-00T23:59:59.000Z

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

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

42

Ozone depletion and health  

SciTech Connect

This book presents the state of knowledge of the ozone layer and the greenhouse effect. Deleterious effects of ultra-violet radiation on humans, animals, and plants are discussed. Alternatives to chloro-fluoro-carbons and political responses to the scientific discoveries are also addressed.

Russell-Jones, R.; Wigley, T.

1989-01-01T23:59:59.000Z

43

Carbon Monoxide Poisoning Avoided Through Weatherization | Department of  

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

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

44

Photochemistry and Transport of Carbon Monoxide in the Middle Atmosphere  

Science Conference Proceedings (OSTI)

Two-dimensional model calculations of the photochemistry and transport of carbon monoxide in the stratosphere, mesosphere, and lower thermosphere are presented. Results are compared to available observations at midlatitudes, where both ...

S. Solomon; R. R. Garcia; J. J. Olivero; R. M. Bevilacqua; P. R. Schwartz; R. T. Clancy; D. O. Muhleman

1985-05-01T23:59:59.000Z

45

Inhibition of Premixed Carbon Monoxide-Hydrogen-Oxygen ...  

Science Conference Proceedings (OSTI)

... The fuel gas is carbon monoxide (Mathe- son UHP, 99.9% CO, with the sum of ... filters) gener- ates the schlieren image of the flame for capture by a ...

2012-09-07T23:59:59.000Z

46

Annual and Seasonal Global Variation in Total Ozone and Layer-Mean Ozone,  

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

Atmospheric Trace Gases » Ozone » Total Ozone and Layer-Mean Ozone Atmospheric Trace Gases » Ozone » Total Ozone and Layer-Mean Ozone Annual and Seasonal Global Variation in Total Ozone and Layer-Mean Ozone, 1958-1987 (1991) DOI: 10.3334/CDIAC/atg.ndp023 data Data Investigators J. K. Angell, J. Korshover, and W. G. Planet Description For 1958 through 1987, this data base presents total ozone variations and layer mean ozone variations expressed as percent deviations from the 1958 to 1977 mean. The total ozone variations were derived from mean monthly ozone values published in Ozone Data for the World by the Atmospheric Environment Service in cooperation with the World Meteorological Organization. The layer mean ozone variations are derived from ozonesonde and Umkehr observations. The data records include year, seasonal and annual

47

OZONE PRECURSORS, SOURCE REGIONS, AND O(3) FORMATION DURING THE TEXAQS 2000 STUDY.  

SciTech Connect

The DOE G-1 aircraft made flights on 14 days during the TexAQS 2000 study. On 7 of those days, the aircraft encountered highly localized plumes exhibiting O{sub 3} concentrations in excess of 150 ppb; on some days, peak O{sub 3} concentrations were in excess of 200 ppb. These ozone plumes were rapidly formed with an efficiency (O{sub 3} per NO{sub x} molecule consumed) much higher (7-20) than observed in other urban areas (3-4), and were frequently associated with high concentrations (>20 ppb) of secondary hydrocarbon species such as formaldehyde. Back trajectory analysis showed that the plumes were invariably associated with emissions from one or more of the large industrial complexes clustered about the Houston Ship Channel and Galveston Bay. Very high hydrocarbon reactivities were found in the vicinity of these facilities during morning flights. These hydrocarbon reactivities, in combination with local NO{sub x} emissions, were large enough to support instantaneous O{sub 3} production rates as high as 200 ppb/h. It is hypothesized that the combination of nitrogen oxides and hydrocarbon emissions emanating from this complex of industries provided a potent mixture of chemicals that caused the rapid formation of very high concentrations of ozone which, depending on the prevailing meteorology, could cause exceedance of the NAAQS ozone standard anywhere in the Houston metropolitan area.

DAUM,P.H.; KLEINMAN,L.I.; BRECHTEL,F.; LEE,Y.N.; NUNNERMACKER,L.J.; SPRINGSTON,S.R.; WEINSTEIN-LLOYD,J.

2001-10-01T23:59:59.000Z

48

Plasma Processing Of Hydrocarbon  

SciTech Connect

The Idaho National Laboratory (INL) developed several patented plasma technologies for hydrocarbon processing. The INL patents include nonthermal and thermal plasma technologies for direct natural gas to liquid conversion, upgrading low value heavy oil to synthetic light crude, and to convert refinery bottom heavy streams directly to transportation fuel products. Proof of concepts has been demonstrated with bench scale plasma processes and systems to convert heavy and light hydrocarbons to higher market value products. This paper provides an overview of three selected INL patented plasma technologies for hydrocarbon conversion or upgrade.

Grandy, Jon D; Peter C. Kong; Brent A. Detering; Larry D. Zuck

2007-05-01T23:59:59.000Z

49

Terpolymerization of ethylene, sulfur dioxide and carbon monoxide  

DOE Patents (OSTI)

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

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

1981-01-01T23:59:59.000Z

50

Hole in the ozone layer?  

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

Hole in the ozone layer? Hole in the ozone layer? Name: Kelley Location: N/A Country: N/A Date: N/A Question: Is there really a hole in the ozone layer? Replies: That depends on what one means by a "hole". There is a thinning of the layer that is particularly severe during certain seasons at the poles. But the ozone layer is thinning most everywhere. The thinning around the south pole of earth is particularly stunning, and has been referred to as a hole even though some ozone still exists there, it is much less concentrated. As you may know, this ozone destruction is probably due to human release of pollutants such as clorofluorocarbons (CFCs) an due to natural sources such as chemicals from volcanic eruptions. CFCs are used is cooling systems such as refrigerators and air conditioning. There is an international agreement to phase out the use of these destructive chemicals but they won't be banned entirely for years for fears of losing money. Meanwhile the ozone layer thins and we are exposed to increasingly higher doses of cancer causing radiation

51

A Smart Sensor System for Carbon Monoxide Detection  

Science Conference Proceedings (OSTI)

This paper illustrates a smart sensor system for carbon monoxide detection. An innovative technological approach has been pursued to fabricate gas sensors on silicon substrate, compatible with IC fabrication. A mixed analog-digital electronic interface processes ... Keywords: sensor interfaces, sensors, sigma-delta converters

G. C. Cardinali; L. Dori; M. Fiorini; I. Sayago; G. Faglia; C. Perego; G. Sberveglieri; V. Liberali; F. Maloberti; D. Tonietto

1997-11-01T23:59:59.000Z

52

Ultraviolet photoelectron spectroscopy of molybdenum and molybdenum monoxide anions  

E-Print Network (OSTI)

of Utah, Salt Lake City, Utah 84112 Received 30 May 1995; accepted 23 October 1995 The 351 nm photoelectron spectra of Mo and MoO have been measured. The electron affinity of atomic molybdenum is 0.748 2 e- denum monoxide illustrates these difficulties especially well, since the molybdenum atomic ground state

Lineberger, W. Carl

53

Hydrocarbon adsorption system  

SciTech Connect

In a solid adsorbent hydrocarbon recovery system for processing natural gas, towers adapted for performing adsorbing, cooling, and regenerating functions are used. It is recommended that a regeneration gas be used of substantially uniform richness in hydrocarbons in the closed-cycle regeneration system. The natural gas stream is flowed through an adsorbent bed to remove liquid hydrocarbons. A portion of the stripped gas stream is flowed through a second adsorbent bed for cooling purposes. A heated, rich, regeneration gas is circulated through a closed-cycle regeneration system that includes a third adsorbent bed. This rich regeneration gas is combined with the stripped gas stream. These steps are repeated in a cyclic operation. (10 claims)

Humphries, C.L.

1966-11-29T23:59:59.000Z

54

Hydrocarbon/Total Combustibles Sensor  

the invention is an electrochemical hydrocarbon sensor that is more reliable and reproducible than any other hydrocarbon sensor on the market today. The patented method for producing the sensor ensures reproducibility and reduces the need for ...

55

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

56

Catalysts for hydrocarbon conversion  

Science Conference Proceedings (OSTI)

Catalyst, particularly useful in catalytic reforming and for producing highly pure aromatic hydrocarbons, comprising an alumina carrier and containing, expressed in proportion of the weight of the alumina carrier: 005 to 1% of platinum 01 to 4% of gallium, indium or thallium 01 to 2% of tungsten, and 1 to 10% of halogen.

Le P. J.; Malmaison, R.; Marcilly, C.; Martino, G.; Miquel, J.

1980-08-12T23:59:59.000Z

57

Hydrocarbon synthesis catalyst and method of preparation and use thereof. [DOE patent application  

DOE Patents (OSTI)

A catalyst for the synthesis of hydrocarbons from carbon monoxide and hydrogen composed of palladium or platinum and cobalt supported on a solid phase is disclosed. The catalyst is prepared by heating a heterogeneous component of the palladium or platinum deposited on the solid support in a solution of cobalt carbonyl or precursors thereof. The catalyst exhibits excellent activity, stability in air, and produces highly desirable product fractions even with dilute gaseous reactants. The catalyst is preferably used in dilute slurry form, which is desirable from a heat transfer standpoint.

Sapienza, R.S.; Sansone, M.J.; Slegeir, W.A.R.

1981-08-14T23:59:59.000Z

58

Hydrocarbon reclaimer system  

SciTech Connect

This patent describes a filtering process for filtering sludge from a finished product oil storage tank and thereby separating solids from oil and hydrocarbon. The process requires no added water, solvents or diluents. It comprises: pumping a volume sludge from a finished product oil storage tank to a mixing tank; mixing the sludge; sampling the sludge to determine solid content; adding filter aid comprising diatomaceous earth to the mixing tank; mixing the filter aid with the sludge in the mixing tank; enclosing and sealing a plurality of filter plates inside a horizontal plate filter; pressurizing the horizontal plate filter by operation of pump means; pumping the sludge from the mixing tank through the horizontal plate filter to filter out solids; recirculating the sludge from the horizontal plate filter back through the mixing tank; and pumping a purified hydrocarbon and water filtrate from the horizontal plate filter.

Uremovich, M.J.

1990-09-04T23:59:59.000Z

59

FROZEN HYDROCARBONS IN COMETS  

SciTech Connect

Recent investigations of the luminescence of frozen hydrocarbon particles of icy cometary halos have been carried out. The process of luminescence of organic icy particles in a short-wavelength solar radiation field is considered. A comparative analysis of observed and laboratory data leads to 72 luminescent emission lines in the spectrum of the comet 153P/Ikeya-Zhang. The concept of cometary relict matter is presented, and the creation of a database of unidentified cometary emission lines is proposed.

Simonia, Irakli, E-mail: irakli.simonia@jcu.edu.au [School of Graduate Studies, Ilia State University, 3/5 Cholokashvili Street, Tbilisi, 0162 (Georgia); Center for Astronomy, James Cook University, Townsville QLD 4811 (Australia)

2011-02-15T23:59:59.000Z

60

THERMOCHEMISTRY OF HYDROCARBON RADICALS  

DOE Green Energy (OSTI)

Gas phase negative ion chemistry methods are employed to determine enthalpies of formation of hydrocarbon radicals that are important in combustion processes and to investigate the dynamics of ion-molecule reactions. Using guided ion beam tandem mass spectrometry, we measure collisional threshold energies of endoergic proton transfer and hydrogen atom transfer reactions of hydrocarbon molecules with negative reagent ions. The measured reaction threshold energies for proton transfer yield the relative gas phase acidities. In an alternative methodology, competitive collision-induced dissociation of proton-bound ion-molecule complexes provides accurate gas phase acidities relative to a reference acid. Combined with the electron affinity of the R {center_dot} radical, the gas phase acidity yields the RH bond dissociation energy of the corresponding neutral molecule, or equivalently the enthalpy of formation of the R{center_dot} organic radical, using equation: D(R-H) = {Delta}{sub acid}H(RH) + EA(R) - IE(H). The threshold energy for hydrogen abstraction from a hydrocarbon molecule yields its hydrogen atom affinity relative to the reagent anion, providing the RH bond dissociation energy directly. Electronic structure calculations are used to evaluate the possibility of potential energy barriers or dynamical constrictions along the reaction path, and as input for RRKM and phase space theory calculations. In newer experiments, we have measured the product velocity distributions to obtain additional information on the energetics and dynamics of the reactions.

Kent M. Ervin, Principal Investigator

2004-08-17T23:59:59.000Z

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.


61

Reclamation and reuse of freon in total petroleum hydrocarbon analyses  

SciTech Connect

ADS is using a commercially available solvent reclamation system to recycle 95-97 percent of the Freon used in total petroleum hydrocarbon analyses. ADS has further developed the commercially available solvent reclamation system to accommodate radioactive contaminated Freon. This report establishes the following: validity of the method; success of recycling; and effect of radionuclides in recycling radioactive contaminated Freon. The standard analysis method for determining total petroleum hydrocarbons (commonly known as oil and grease determination) involves solvent extraction of the hydrocarbons using Freon followed by quantitation using infrared detection. This has been the method of choice because it is simple, rugged, inexpensive, and applicable to both solid and liquid samples and to radioactive samples. Due to its deleterious effect on the ozone layer, the use of Freon and other chloro-fluorocarbons (CFCs) has been greatly restricted. Freon has become very expensive (800$/liter) and will soon be unavailable entirely. Several methods have been proposed to replace the Freon extraction method. These methods include solid-phase extraction, solvent extraction, and supercritical fluid extraction all of which use gravimetric determination or infrared analysis of the extracted hydrocarbons. These methods are not as precise or as sensitive as the Freon extraction method, and a larger amount of sample is therefore required due to the decreased sensitivity. The solid phase extraction method cannot accommodate solid samples. Supercritical fluid extraction requires expensive instrumentation. ADS opted to keep the existing Freon method and recycle the solvent. An inexpensive solvent reclamation system was procured to reclaim the spent Freon. This reclaimer removes hydrocarbons from the Freon solvent by passage through an activated carbon bed.

Ekechukwu, A.A.; Peterson, S.F.

1996-04-01T23:59:59.000Z

62

Ozone Conference II: Abstract Proceedings  

Science Conference Proceedings (OSTI)

Ozone Conference II: Pre- and Post-Harvest Applications Two Years After Gras, was held September 27-28, 1999 in Tulare, California. This conference, sponsored by EPRI's Agricultural Technology Alliance and Southern California Edison's AgTAC facility, was coordinated and organized by the on-site ATA-AgTAC Regional Center. Approximately 175 people attended the day-and-a-half conference at AgTAC. During the Conference twenty-two presentations were given on ozone food processing and agricultural applications...

1999-11-24T23:59:59.000Z

63

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

E-Print Network (OSTI)

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

Smieja, Jonathan Mark

2012-01-01T23:59:59.000Z

64

Carbon monoxide study - Seattle, Washington, October 6-November 2, 1977. Part 1. Executive summary report  

SciTech Connect

This report is a summary of EPA 910/9-78-054b, a study of the carbon monoxide problem in downtown Seattle.

Wilson, C.B.; Schweiss, J.W.

1978-12-01T23:59:59.000Z

65

A Comparison of Total Column Ozone Values Derived from the Global Ozone Monitoring Experiment (GOME), the Tiros Operational Vertical Sounder (TOVS), and the Total Ozone Mapping Spectrometer (TOMS)  

Science Conference Proceedings (OSTI)

A comparison of total column ozone data retrieved from the Global Ozone Monitoring Experiment (GOME), the Tiros Operational Vertical Sounder (TOVS), and the Total Ozone Mapping Spectrometer (TOMS) for the years 1996, 1997, 1998, and 1999 is ...

Gary K. Corlett; Paul S. Monks

2001-05-01T23:59:59.000Z

66

Ozone Reductions Using Residential Building Envelopes  

SciTech Connect

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

67

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

E-Print Network (OSTI)

hydrocarbons (toluene), alkanes (butane, methane, heptane),tube/GC (NIOSH 1 5 0 0 ) a Butane 300ppm Charcoal tube/GC (O toluene toluene + C O butane butane + C O methane methane

Apte, Michael G.

2010-01-01T23:59:59.000Z

68

HYDROCARBON LIQUID FLOW CALIBRATION SERVICE ...  

Science Conference Proceedings (OSTI)

... and is the cross correlation coefficient ... a NIST Hydrocarbon Liquid Flow Calibration Facility ... FED2004-56790, 2004 Heat Transfer/Fluids Engineering ...

2012-05-21T23:59:59.000Z

69

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

DOE Green Energy (OSTI)

Several different catalytic reactions must be carried out in order to convert hydrocarbons (or alcohols) into hydrogen for use as a fuel for polyelectrolyte membrane (PEM) fuel cells. Each reaction in the fuel-processing sequence has a different set of characteristics, which influences the type of catalyst support that should be used for that particular reaction. A wide range of supports are being evaluated for the various reactions in the fuel-processing scheme, including porous and non-porous particles, ceramic and metal straight-channel monoliths, and ceramic and metal monolithic foams. These different types of support have distinctly different transport characteristics. The best choice of support for a given reaction will depend on the design constraints for the system, e.g., allowable pressure drop, and on the characteristics of the reaction for which the catalyst is being designed. Three of the most important reaction characteristics are the intrinsic reaction rate, the exothermicity/endothermicity of the reaction, and the nature of the reaction network, e.g., whether more than one reaction takes place and, in the case of multiple reactions, the configuration of the network. Isotopic transient kinetic analysis was used to study the surface intermediates. The preferential oxidation of low concentrations of carbon monoxide in the presence of high concentrations of hydrogen (PROX) is an important final step in most fuel processor designs. Data on the behavior of straight-channel monoliths and foam monolith supports will be presented to illustrate some of the factors involved in choosing a support for this reaction.

Mr. Paul Chin; Dr. Xiaolei Sun; Professor George W. Roberts; Professor James J. Spivey; Mr. Amornmart Sirijarhuphan; Dr. James G. Goodwin, Jr.; Dr. Richard W. Rice

2002-12-31T23:59:59.000Z

70

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.

71

717 Notices to Readers Carbon Monoxide Poisoning Deaths  

E-Print Network (OSTI)

Carbon Monoxide monoxide Poisoning (CO) is an odorless, — Continued colorless, nonirritating gas produced by the incomplete combustion of carbon-based fuels. CO exposure is responsible for more fatal unintentional poisonings in the United States than any other agent, with the highest incidence occurring during the cold-weather months (1). Although most of these deaths occur in residences or motor vehicles (2), two incidents among campers in Georgia illustrate the danger of CO in outdoor settings. This report describes the two incidents, which resulted in six deaths, and provides recommendations for avoiding CO poisoning in outdoor settings. Cases 1–4. On the afternoon of March 14, 1999, a 51-year-old man, his 10-year-old son, a 9-year-old boy, and a 7-year-old girl were found dead inside a zipped-up, 10-foot by 14-foot, two-room tent at their campsite in southeast Georgia (a pet dog also died). A propane gas stove, still burning, was found inside the tent; the stove apparently had been brought inside to provide warmth. The occupants had died during the night. Postmortem carboxyhemoglobin (COHb) levels measured 50%, 63%, 69%, and 63%, respectively, in the four decedents (in the general U.S. population, COHb concentrations

Basidiobolomycosis Arizona; North Carolinia

1999-01-01T23:59:59.000Z

72

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

73

Antarctic Ozone Transport and Depletion in Austral Spring 2002  

Science Conference Proceedings (OSTI)

The ozone budget in the Antarctic region during the stratospheric warming in 2002 is studied, using ozone analyses from the Royal Netherlands Meteorological Institute (KNMI) ozone-transport and assimilation model called TM3DAM. The results show a ...

Peter Siegmund; Henk Eskes; Peter van Velthoven

2005-03-01T23:59:59.000Z

74

Interaction of carbon monoxide and hydrogen with the (1010) face of ruthenium  

DOE Green Energy (OSTI)

The interaction was studied at 23.5, 200, and -135/sup 0/C with low energy electron diffraction (LEED) and Auger electron spectroscopy. (AES). Carbon monoxide adsorbs associatively at 23.5/sup 0/C, but is apparently dissociated by the LEED beam and hydrogen adsorbed from the ambient after a few minutes for less than 10 Langmuirs of carbon monoxide. For large doses of carbon monoxide at 23.5/sup 0/C, 10 Langmuirs or more, the LEED beam does not disociate carbon monoxide, but carbon monoxide and hydrogen adsorbed from the ambient do appear to be removed from the surface by the LEED beam. Carbon monoxide and hydrogen on the surface together will react and form surface complexes with distinctive LEED patterns at 23.5/sup 0/C though some of the interactions appear to be LEED beam induced. If sufficient hydrogen is present, some of these complexes are lost from the surface probably as methane and water. Carbon monoxide will react with itself and hydrogen at 23.5/sup 0/C with carbon being lost from the surface probably as carbon dioxide. At 200/sup 0/C, neither carbon monoxide nor hydrogen will absorb on Ru (1010) in significant amounts at the low dose pressures used. However, if the Ru(1010) crystal is allowed to cool below 70/sup 0/C, ambient carbon monoxide and hydrogen will adsorb on Ru (1010) and form LEED patterns like those formed at 23.5/sup 0/C. At -135/sup 0/C, carbon monoxide will react with itself and hydrogen readily most of the time producing surface complexes with distinctive LEED paterns. If a moderate amount of hydrogen is present, some of these complexes are lost from the surface, probably as methane. If a large amount of hydrogen is present, some of these complexes are lost from the surface probably as carbon dioxdie. 17 figures, 8 tables.

Tomcsik, T.L.

1979-01-01T23:59:59.000Z

75

Laboratory measurement of secondary pollutant yields from ozone...  

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

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

76

Calibration of the Ogawa ozone passive sampler for aircraft cabins...  

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

Calibration of the Ogawa ozone passive sampler for aircraft cabins. Title Calibration of the Ogawa ozone passive sampler for aircraft cabins. Publication Type Journal Article Year...

77

Iron catalysis in oxidation by ozone - Energy Innovation Portal  

Bookmark Iron catalysis in oxidation by ozone - Energy Innovation Portal on Google; Bookmark Iron catalysis in oxidation by ozone - Energy Innovation ...

78

Y-12 Plant Stratospheric Ozone Protection plan  

SciTech Connect

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

79

Hydrocarbon Source Signatures in Houston, Texas: Influence of the Petrochemical Industry  

SciTech Connect

Observations of C1-C10 hydrocarbon mixing ratios measured by in-situ instrumentation at the La Porte super site during the TexAQS 2000 field experiment are reported. The La Porte data were compared to a roadway vehicle exhaust signature obtained from canister samples collected in the Houston Washburn tunnel during the same summer to better understand the impact of petrochemical emissions of hydrocarbons at the site. It is shown that the abundance of ethene, propene, 1-butene, C2-C4 alkanes, hexane, cyclohexane, methylcyclohexane, isopropylbenzene, and styrene at La Porte were systematically impacted by petrochemical industry emissions. Coherent power law relationships between frequency distribution widths of hydrocarbon mixing ratios and their local lifetimes clearly identify two major source groups, roadway vehicle emissions and industrial emissions. Distributions of most aromatics and long chain alkanes were consistent with roadway vehicle emissions as the dominant source. Airmass reactivity was generally dominated by C1-C3 aldehydes. Propene and ethene sometimes dominated air mass reactivity with HO loss frequencies often greater than 10 s-1. Ozone mixing ratios near 200 ppbv were observed on two separate occasions and these air masses appear to have been impacted by industrial emissions of alkenes from the Houston Ship Channel. The La Porte data provide evidence of the importance of industrial emissions of ethene and propene on air masses reactivity and ozone formation in Houston.

Jobson, B Tom T.; Berkowitz, Carl M.; Kuster, W. C.; Goldan, P. D.; Williams, E. J.; Fesenfeld, F.; Apel, Eric; Karl, Thomas G.; Lonneman, William A.; Riemer, D.

2004-12-22T23:59:59.000Z

80

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

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

Size Effect of Ruthenium Nanoparticles in Catalytic Carbon Monoxide Oxidation  

Science Conference Proceedings (OSTI)

Carbon monoxide oxidation over ruthenium catalysts has shown an unusual catalytic behavior. Here we report a particle size effect on CO oxidation over Ru nanoparticle (NP) catalysts. Uniform Ru NPs with a tunable particle size from 2 to 6 nm were synthesized by a polyol reduction of Ru(acac){sub 3} precursor in the presence of poly(vinylpyrrolidone) stabilizer. The measurement of catalytic activity of CO oxidation over two-dimensional Ru NPs arrays under oxidizing reaction conditions (40 Torr CO and 100 Torr O{sub 2}) showed an activity dependence on the Ru NP size. The CO oxidation activity increases with NP size, and the 6 nm Ru NP catalyst shows 8-fold higher activity than the 2 nm catalysts. The results gained from this study will provide the scientific basis for future design of Ru-based oxidation catalysts.

Joo, Sang Hoon; Park, Jeong Y.; Renzas, J. Russell; Butcher, Derek R.; Huang, Wenyu; Somorjai, Gabor A.

2010-04-04T23:59:59.000Z

82

Hydrocarbons in the deep earth  

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

composed of the elements hydrogen and carbon) are the main building block of crude oil and natural gas. Hydrocarbons contribute to the global carbon cycle (one of the most...

83

Hydrocarbon adsorption apparatus and process  

SciTech Connect

A method of recovering hydrocarbons from natural gas by the use of solid adsorbents consists of 3 steps. The main flow stream of natural gas is passed through a first and only bed of solid adsorbent so that at least a portion of the hydrocarbons present is adsorbed in the bed. A heated regeneration gas is next passed through a second bed of solid adsorbent so that at least a portion of the hydrocarbons is desorbed from the bed. The main flow of natural gas is passed through the second and only bed when in a heated condition after regeneration and the flow of heated regeneration gas is passed through the first bed. The hydrocarbons desorbed from the first and second beds from the regeneration gas are recovered while the previous 3 steps are repeated. (6 claims)

Humphries, C.L.

1966-12-06T23:59:59.000Z

84

Optimal statistical model for forecasting ozone  

Science Conference Proceedings (OSTI)

The objective of this paper is to apply time series analysis and multiple regression method to ozone data in order to obtain the optimal statistical model for forecasting next day ozone level. The best estimated model is then used to produce one-step ... Keywords: ARMA (p, q), Durbin-Watson Statistic, MAPE, R-square, multiple regression

M. Abdollahian; R. Foroughi; N. Debnath

2006-04-01T23:59:59.000Z

85

Modeling Ambient Carbon Monoxide Trends to Evaluate Mobile Source Emissions Reductions  

Science Conference Proceedings (OSTI)

Regression models have been used with poor success to detect the effect of emission control programs in ambient concentration measurements of carbon monoxide. An advanced CO regression model is developed whose form is based on an understanding of ...

Robin L. Dennis; Mary W. Downton

1987-10-01T23:59:59.000Z

86

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

87

Basin-Scale Carbon Monoxide Distributions in the Parallel Ocean Program  

Science Conference Proceedings (OSTI)

As a primary photochemical constituent in upper-ocean and tropospheric geocycling, carbon monoxide is of interest to a variety of global change research communities. Dynamic three-dimensional simulations of its marine concentration patterns, ...

Shaoping Chu; Scott Elliott; David Erickson

2007-12-01T23:59:59.000Z

88

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

89

Ozone, skin cancer, and the SST  

SciTech Connect

In 1971, the U.S. Congress cut off funding for development of supersonic transport aircraft prototypes when it was argued that the pollution created by SSTs could reduce the stratospheric ozone content and increase the incidence of skin cancer. At present, the theory of ozone depletion is in a rather uncertain state. Two examples of this are cited. First, ozone depletion may depend more on the availability of surfaces of aerosols and particles than on the content of chlorine. Second, it has been discovered that NO(x) can tie up active chlorine and thus reduce depletion from that source. We are therefore left with the paradoxical result that under certain circumstances SSTs flying in the lower stratospheric can actually counteract, at least partially, any ozone-depleting effects of CFCs. A recent study by scientists at the Brookhaven National Laboratory showed that melanoma rates would not be affected by changes in the ozone layer. If these results are confirmed, then much of the fear associated with ozone depletion disappears. It is difficult to tell how all this will affect a future supersonic transport program, since it is not clear whether a fleet of SSTs will increase or offset ozone depletion.

Singer, S.F.

1994-07-01T23:59:59.000Z

90

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

DOE Green Energy (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

91

Conversion of Mixed Oxygenates Generated from Synthesis Gas to Fuel Range Hydrocarbon  

SciTech Connect

The growing dependence in the U.S. on foreign crude oil supplies and increased concerns regarding greenhouse gas emission has generated considerable interest in research to develop renewable and environmentally friendly liquid hydrocarbon transportation fuels. One of the strategies for achieving this is to produce intermediate compounds such as alcohols and other simple oxygenates from biomass generated synthesis gas (mixture of carbon monoxide and hydrogen) and further convert them into liquid hydrocarbons. The focus of this research is to investigate the effects of mixed oxygenates intermediate product compositions on the conversion step to produce hydrocarbon liquids. A typical mixed oxygenate stream is expected to contain water (around 50%), alcohols, such as methanol and ethanol (around 35%), and smaller quantities of oxygenates such as acetaldehyde, acetic acid and ethyl acetate. However the ratio and the composition of the mixed oxygenate stream generated from synthesis gas vary significantly depending on the catalyst used and the process conditions. Zeolite catalyzed deoxygenation of methanol accompanied by chain growth is well understood under Methanol-to-Gasoline (MTG) like reaction conditions using an H-ZSM-5 zeolite as the catalyst6-8. Research has also been conducted to a limited extent in the past with higher alcohols, but not with other oxygenates present9-11. Also there has been little experimental investigation into mixtures containing substantial amounts of water. The latter is of particular interest because water separation from the hydrocarbon product would be less energy intensive than first removing it from the oxygenate intermediate stream prior to hydrocarbon synthesis, potentially reducing overall processing costs.

Ramasamy, Karthikeyan K.; Gerber, Mark A.; Lilga, Michael A.; Flake, Matthew D.

2012-08-19T23:59:59.000Z

92

Discovery of carbon monoxide in the upper atmosphere of Pluto  

E-Print Network (OSTI)

Pluto's icy surface has changed colour and its atmosphere has swelled since its last closest approach to the Sun in 1989. The thin atmosphere is produced by evaporating ices, and so can also change rapidly, and in particular carbon monoxide should be present as an active thermostat. Here we report the discovery of gaseous CO via the 1.3mm wavelength J=2-1 rotational transition, and find that the line-centre signal is more than twice as bright as a tentative result obtained by Bockelee-Morvan et al. in 2000. Greater surface-ice evaporation over the last decade could explain this, or increased pressure could have caused the atmosphere to expand. The gas must be cold, with a narrow line-width consistent with temperatures around 50 K, as predicted for the very high atmosphere, and the line brightness implies that CO molecules extend up to approximately 3 Pluto radii above the surface. The upper atmosphere must have changed markedly over only a decade since the prior search, and more alterations could occur by the...

Greaves, J S; Friberg, P

2011-01-01T23:59:59.000Z

93

Cleanup of hydrocarbon conversion system  

Science Conference Proceedings (OSTI)

This patent describes a process for the catalytic reforming of a substantially contaminant-free second hydrocarbon feed using a second reforming catalyst, in a catalytic-reforming system having equipment contaminated through contact with a contaminant-containing prior feed. It comprises: contacting the first hydrocarbon feed in the catalytic-reforming system at first reforming conditions with a first reforming catalyst until contaminant removal from the conversion system is substantially completed and the system is contaminant-free; thereafter replacing the first reforming catalyst in the contaminant-free catalytic-reforming system with a second reforming catalyst; and thereafter contacting the second hydrocarbon feed in the contaminant-free catalytic-reforming system with the second reforming catalyst at second reforming conditions.

Peer, R.L.; Russ, M.B.

1990-07-10T23:59:59.000Z

94

Enrichment of light hydrocarbon mixture  

Science Conference Proceedings (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

95

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)

2010-08-10T23:59:59.000Z

96

Biological enhancement of hydrocarbon extraction  

SciTech Connect

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

97

Baseline Ozone Results from 1923 to 1955  

Science Conference Proceedings (OSTI)

Baseline total atmospheric ozone values have been derived, using the Chappuis band, from historical data for 11 Smithsonian sites, including both Northern and Southern Hemispheres. The main baselines consist of 1194 and 970 days respectively for ...

Ronald J. Angione; Robert G. Roosen

1983-08-01T23:59:59.000Z

98

Climatological effects of atmospheric ozone: A review  

Science Conference Proceedings (OSTI)

The paper presents some results of model estimates of ozone (O/sub 3/) climatological effects. Specific issues involved in O/sub 3/ climate study and future research needs are discussed. (ACR)

Wang, W.C.

1984-01-01T23:59:59.000Z

99

Tropospheric Ozone in Louisiana and Synoptic Circulation  

Science Conference Proceedings (OSTI)

Tropospheric ozone (O3) is a pollutant of increasing concern in many urban areas in the United States. There is an increasing need to understand the geographical and meteorological properties associated with O3, particularly because of the ...

Robert V. Rohli; Michelle M. Russo; Anthony J. Vega; John B. Cole

2004-10-01T23:59:59.000Z

100

Catalytic Conversion of Bioethanol to Hydrocarbons ...  

Conventional biomass to hydrocarbon conversion is generally not commercially feasible, due to costs of the conversion process.

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

Hydrocarbons from plants and trees  

DOE Green Energy (OSTI)

The way energy was used in the US in 1980 was examined. A diagram shows the development of energy from its source to its end use. The following are described: the carbon dioxide problem - the greenhouse effect, sugar cane as an energy source, hydrocarbon-producing plants and trees, and isoprenoids from plants and trees. (MHR)

Calvin, M.

1982-07-01T23:59:59.000Z

102

Global Variation in Total Ozone and Layer-Mean Ozone: An Update Through 1981  

Science Conference Proceedings (OSTI)

Total-ozone variations have been updated through 1981 for four regions in north temperate latitudes, the five climatic zones, both hemispheres, and the world. Also updated through 1981 are ozone values in height layers 32–48 km, 24–32 km, 16–24 ...

J. K. Angell; J. Korshover

1983-09-01T23:59:59.000Z

103

Syngas Upgrading to Hydrocarbon Fuels Technology Pathway  

DOE Green Energy (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

104

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

SciTech Connect

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

105

Substantially isotactic, linear, alternating copolymers of carbon monoxide and an olefin  

DOE Patents (OSTI)

The compound, [Pd(Me-DUPHOS)(MeCN){sub 2}](BF{sub 4}){sub 2}, [Me-DUPHOS: 1,2-bis(2,5-dimethylphospholano)benzene] is an effective catalyst for the highly enantioselective, alternating copolymerization of olefins, such as aliphatic {alpha}-olefins, with carbon monoxide to form optically active, isotactic polymers which can serve as excellent starting materials for the synthesis of other classes of chiral polymers. For example, the complete reduction of a propylene-carbon monoxide copolymer resulted in the formation of a novel, optically active poly(1,4-alcohol). Also, the previously described catalyst is a catalyst for the novel alternating isomerization cooligomerization of 2-butene with carbon monoxide to form optically active, isotactic poly(1,5-ketone).

Sen, A.; Jiang, Z.

1996-05-28T23:59:59.000Z

106

Substantially isotactic, linear, alternating copolymers of carbon monoxide and an olefin  

DOE Patents (OSTI)

The compound, [Pd(Me-DUPHOS)(MeCN).sub.2 ](BF.sub.4).sub.2, [Me-DUPHOS: 1,2-bis(2,5-dimethylphospholano)benzene] is an effective catalyst for the highly enantioselective, alternating copolymerization of olefins, such as aliphatic .alpha.-olefins, with carbon monoxide to form optically active, isotactic polymers which can serve as excellent starting materials for the synthesis of other classes of chiral polymers. For example, the complete reduction of a propylene-carbon monoxide copolymer resulted in the formation of a novel, optically active poly(1,4-alcohol). Also, the previously described catalyst is a catalyst for the novel alternating isomerization cooligomerization of 2-butene with carbon monoxide to form optically active, isotactic poly(1,5-ketone)

Sen, Ayusman (State College, PA); Jiang, Zhaozhong (State College, PA)

1996-01-01T23:59:59.000Z

107

Effects of Ozone Heating on Forced Equatorial Kelvin Waves  

Science Conference Proceedings (OSTI)

An equatorial beta-plane model of the stratosphere is used to examine the effects of longwave radiational cooling, ozone photochemistry, and ozone advection on the linear spatial modulation of forced equatorial Kelvin waves. The model atmosphere ...

Robert S. Echols; Terrence R. Nathan

1996-01-01T23:59:59.000Z

108

Relations between Meteorology and Ozone in the Lake Michigan Region  

Science Conference Proceedings (OSTI)

The field program phase of the Lake Michigan Ozone Study (LMOS) took place during the summer of 1991. Observed ozone concentrations and weather variables have been analyzed for the Lake Michigan region and the eastern United States for four 1991 ...

Steven R. Hanna; Joseph C. Chang

1995-03-01T23:59:59.000Z

109

Determination of Total Ozone Amount from TIROS Radiance Measurements  

Science Conference Proceedings (OSTI)

Total ozone amounts are determined from atmospheric radiances measured by the TIROS Operational Vertical Sounder (TOVS). The retrieval procedure is one of linear regression where total ozone amounts derived from Dobson spectrophotometer ...

Walter G. Planet; David S. Crosby; James H. Lienesch; Michael L. Hill

1984-02-01T23:59:59.000Z

110

Vertical Structure of the Anomalous 2002 Antarctic Ozone Hole  

Science Conference Proceedings (OSTI)

Ozone estimates from observations by the NOAA-16 Solar Backscattered Ultraviolet (SBUV/2) instrument and Television Infrared Observation Satellite (TIROS-N) Operational Vertical Sounder (TOVS) are used to describe the vertical structure of ozone ...

S. Kondragunta; L. E. Flynn; A. Neuendorffer; A. J. Miller; C. Long; R. Nagatani; S. Zhou; T. Beck; E. Beach; R. McPeters; R. Stolarski; P. K. Bhartia; M. T. DeLand; L.-K. Huang

2005-03-01T23:59:59.000Z

111

Surface Ozone During the Second Half of the Nineteenth Century  

Science Conference Proceedings (OSTI)

During the last few years, increases in tropospheric ozone concentration have been detected and the need for more study has been recognized. There is very little knowledge about surface ozone background concentrations prior to the advent of ...

Rumen D. Bojkov

1986-03-01T23:59:59.000Z

112

Space and Time Scales in Ambient Ozone Data  

Science Conference Proceedings (OSTI)

This paper describes the characteristic space and time scales in time series of ambient ozone data. The authors discuss the need and a methodology for cleanly separating the various scales of motion embedded in ozone time series data, namely, ...

S. T. Rao; I. G. Zurbenko; R. Neagu; P. S. Porter; J. Y. Ku; R. F. Henry

1997-10-01T23:59:59.000Z

113

Iron Catalysis in Oxidations by Ozone - Energy Innovation Portal  

Wind Energy; Partners (27) Visual Patent Search; Success Stories; News; Events; Industrial Technologies Iron Catalysis in Oxidations by Ozone Ames ...

114

Hydrocarbon Technologies | Open Energy Information  

Open Energy Info (EERE)

Hydrocarbon Technologies Hydrocarbon Technologies Place Lawrenceville, New Jersey Zip 8648 Sector Efficiency Product String representation "Technology-base ... onmental risks." is too long. Coordinates 36.761678°, -77.845048° Loading map... {"minzoom":false,"mappingservice":"googlemaps3","type":"ROADMAP","zoom":14,"types":["ROADMAP","SATELLITE","HYBRID","TERRAIN"],"geoservice":"google","maxzoom":false,"width":"600px","height":"350px","centre":false,"title":"","label":"","icon":"","visitedicon":"","lines":[],"polygons":[],"circles":[],"rectangles":[],"copycoords":false,"static":false,"wmsoverlay":"","layers":[],"controls":["pan","zoom","type","scale","streetview"],"zoomstyle":"DEFAULT","typestyle":"DEFAULT","autoinfowindows":false,"kml":[],"gkml":[],"fusiontables":[],"resizable":false,"tilt":0,"kmlrezoom":false,"poi":true,"imageoverlays":[],"markercluster":false,"searchmarkers":"","locations":[{"text":"","title":"","link":null,"lat":36.761678,"lon":-77.845048,"alt":0,"address":"","icon":"","group":"","inlineLabel":"","visitedicon":""}]}

115

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

116

OZONE PRODUCTION IN URBAN PLUMES.  

SciTech Connect

Ozone levels observed during a field campaign in Houston were significantly higher than that observed in Phoenix or Philadelphia. An examination of the slope of O{sub x} versus NO{sub z} in the urban plumes shows that NO{sub x} is used 2 to 3 times more efficiently in Houston as compared with Phoenix and Philadelphia. Representative values of OPEx are 7-12, 3, and 4, in Houston, Phoenix, and Philadelphia. Aircraft observations have been used to calculate P(O{sub 3})/P(NO{sub z}). Values in Houston are significantly higher than in Phoenix and Philadelphia. We show that P(O{sub 3})/P(NO{sub z}) is proportional to a VOC/NO{sub 2}-OH reactivity ratio. High values of P(O{sub 3})/P(NO{sub z}) in Houston are due to emissions of reactive olefins from the ship channel region. It is significant that high values of P(O{sub 3})/P(NO{sub z}) occur at NO{sub x} levels up to several 10's of ppb. Not only is the chemistry efficient but it will be long lasting. The occurrence of high NO{sub x} and high OPEx is fostered by the co-location of VOC and NO{sub x} sources in the Houston industrial areas.

KLEINMAN,L.

2001-09-17T23:59:59.000Z

117

Deep desulfurization of hydrocarbon fuels  

SciTech Connect

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

118

Ozonization of humic acids in brown coal oxidized in situ  

SciTech Connect

The effect of the ozonization of humic acids in chloroform and glacial acetic acid media on the yield and component composition of the resulting products was studied. The high efficiency of ozonization in acetic acid was found. Water-soluble low-molecular-weight substances were predominant among the ozonization products.

S.A. Semenova; Yu.F. Patrakov; M.V. Batina [Russian Academy of Sciences, Kemerovo (Russia). Institute of Coal and Coal Chemistry

2008-10-15T23:59:59.000Z

119

Liquid-phase ozonation of fusainized components of SS coal  

SciTech Connect

Stepwise ozonation of leaning fusainized components of fossil coal of SS grade in acetic acid was studied. The dynamics of accumulation of oxygen-containing groups in the course of ozonation was examined, and the main pathways of the reaction of ozone with structural fragments of the coal substance were revealed.

Semenova, S.A.; Patrakov, Y.F. [Russian Academy of Sciences, Kemerovo (Russian Federation)

2007-11-15T23:59:59.000Z

120

AMBIENT HYDROCARBONS IN THE HOUSTON METROPOLITAN AREA DURING TEXAQS 2000: AN IDENTIFICATION OF UNUSUAL FEATURES.  

SciTech Connect

Houston's ozone problem has been linked to the occurrence of very high light olefin concentrations. We have analyzed the DOE G-1 aircraft hydrocarbon data set to provide additional information on the geographic distribution and prevalence of air samples with high olefin concentration as well as an identification of other compounds which contribute to the high hydrocarbon reactivity in Houston. In order to identify high concentrations we need a definition of normal. For that purpose we use aircraft samples collected during a 1999 aircraft based field campaign in Philadelphia relying on the circumstance that the frequency distributions of NO{sub x} and C{sub 2}H{sub 2} in Philadelphia are nearly the same as in Houston. Comparison is made also with hydrocarbons collected in Phoenix which exhibit nearly the same NO{sub x} and C{sub 2}H{sub 2} frequency distribution as the other 2 cities, but in spite of that similarity have a much lower hydrocarbon reactivity. As in other studies we find that there is a subset of Houston hydrocarbon samples with very high OH-reactivity due to elevated concentrations of ethylene, propylene and less often butenes, including 1,3 butadiene. Although these samples stand out as being qualitatively different we present evidence that ethylene and propylene are significantly elevated in at least half of the Houston samples, covering a wide geographic area apart from the Ship Channel region. Frequency distributions for these compounds are log normal suggesting that Houston's atmosphere is a single entity rather than separate industrial and urban areas. The comparison between Houston and Philadelphia also identifies C{sub 2}-C{sub 5} alkanes, n-hexane, and benzene as having elevated concentrations. Emission reductions of these less reactive compounds sufficient to yield the concentrations observed in Philadelphia would have a minor effect on the most reactive samples, but about a 20% effect on samples with more typical (median) reactivity.

KLEINMAN, L.I.; DAUM P.H.

2004-11-01T23:59:59.000Z

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.


121

Effect of Ventilation Strategies on Residential Ozone Levels  

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

Effect of Ventilation Strategies on Residential Ozone Levels Effect of Ventilation Strategies on Residential Ozone Levels Title Effect of Ventilation Strategies on Residential Ozone Levels Publication Type Journal Article LBNL Report Number LBNL-5889E Year of Publication 2012 Authors Walker, Iain S., and Max H. Sherman Journal Building and Environment Volume 59 Start Page 456 Pagination 456-465 Date Published 01/2013 Keywords ashrae standard 62,2, filtration, infiltration, mechanical ventilation, ozone, simulation Abstract Elevated outdoor ozone levels are associated with adverse health effects. Because people spend the vast majority of their time indoors, reduction in indoor levels of ozone of outdoor origin would lower population exposures and might also lead to a reduction in ozone---associated adverse health effects. In most buildings, indoor ozone levels are diminished with respect to outdoor levels to an extent that depends on surface reactions and on the degree to which ozone penetrates the building envelope. Ozone enters buildings from outdoors together with the airflows that are driven by natural and mechanical means, including deliberate ventilation used to reduce concentrations of indoor---generated pollutants. When assessing the effect of deliberate ventilation on occupant health one should consider not only the positive effects on removing pollutants of indoor origin but also the possibility that enhanced ventilation might increase indoor levels of pollutants originating outdoors. This study considers how changes in residential ventilation that are designed to comply with ASHRAE Standard 62.2 might influence indoor levels of ozone. Simulation results show that the building envelope can contribute significantly to filtration of ozone. Consequently, the use of exhaust ventilation systems is predicted to produce lower indoor ozone concentrations than would occur with balanced ventilation systems operating at the same air---exchange rate. We also investigated a strategy for reducing exposure to ozone that would deliberately reduce ventilation rates during times of high outdoor ozone concentration while still meeting daily average ventilation requirements.

122

HYDROCARBON AND SULFUR SENSORS FOR SOFC SYSTEMS  

DOE Green Energy (OSTI)

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

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

2003-11-01T23:59:59.000Z

123

Indonesia Forest Fires Exacerbate Carbon Monoxide Pollution over Peninsular Malaysia during July to September 2005  

Science Conference Proceedings (OSTI)

Wind carried the smoke further afield from forest fires in Sumatra caused worse air pollution in Malaysia reached extremely hazardous levels and forced schools and an airport to close. There were 3,258 'hot spots' recorded by NOAA satellites in the province ... Keywords: AIRS, Carbon monoxide, Peninsular

Jasim M. Rajab; M. Z. MatJafri; H. S. Lim; K. Abdullah

2009-08-01T23:59:59.000Z

124

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

125

Compressed Air Sample Technology for Isotopic Analysis of Atmospheric Carbon Monoxide  

Science Conference Proceedings (OSTI)

A methodology for the collection of large (1000 L) air samples for isotopic analysis of atmospheric carbon monoxide is presented. A low-background, high-pressure, high-flow sampling system with a residual background of less than 2 ppbv CO has ...

John E. Mak; Carl A. M. Brenninkmeijer

1994-04-01T23:59:59.000Z

126

Catalytic Conversion of Bioethanol to Hydrocarbons  

ORNL 2011-G00219/jcn UT-B ID 201002414 08.2011 Catalytic Conversion of Bioethanol to Hydrocarbons Technology Summary A method for catalytically converting an alcohol ...

127

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

128

Catalytic Conversion of Bioethanol to Hydrocarbons  

ORNL 2011-G00219/jcn UT-B ID 201002414 08.2011 Catalytic Conversion of Bioethanol to Hydrocarbons Technology Summary A method for catalytically ...

129

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

130

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

131

Method for producing low-cost, high volume hydrogen from hydrocarbon sources  

DOE Patents (OSTI)

A method is described for the conversion of naturally-occurring or biomass-derived lower to higher hydrocarbon (C{sub x}H{sub y},where x may vary from 1--3 and y may vary from 4--8) to low-cost, high-volume hydrogen. In one embodiment, methane, the major component of natural gas, is reacted in a single reaction zone of a mixed-conducting ceramic membrane reactor to form hydrogen via simultaneous partial oxidation and water gas shift reactions at temperatures required for thermal excitations of the mixed-conducting membranes. The hydrogen is produced by catalytically reacting the hydrocarbon with oxygen to form synthesis gas (a mixture of carbon monoxide and hydrogen), followed by a water gas shift (WGS) reaction with steam, wherein both reactions occur in a single reaction zone having a multi-functional catalyst or a combination of catalysts. The hydrogen is separated from other reaction products by membrane-assisted transport or by pressure-swing adsorption technique. Membrane-assisted transport may occur via proton transfer or molecular sieving mechanisms.

Bose, Arun C.; Balachandran, Uthamalinga; Kleerfisch, Mark S.; Udovich, Carl A.; Stiegel, Gary J.

1997-12-01T23:59:59.000Z

132

OXIDATION OF DRY HYDROCARBONS AT HIGH-POWER DENSITY ANODES  

DOE Green Energy (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

133

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.

134

Surface Ozone Pattern in Hong Kong  

Science Conference Proceedings (OSTI)

Surface ozone (O3) and its precursors in rural and urban areas of Hong Kong are analyzed through the seasonal, temporal, and spatial variation patterns. The seasonal O3 shows a unique pattern with a major peak in autumn and a trough in summer. ...

L. Y. Chan; C. Y. Chan; Y. Qin

1998-10-01T23:59:59.000Z

135

Ozone Conservation and Entrainment in Cumulus Congestus  

Science Conference Proceedings (OSTI)

This study demonstrates that ozone mixing ratio (O3) is conserved during moist convection and can be used as a tracer for cloud entrainment studies. The approach used is to apply mixing line analysis to pairs of liquid water potential temperature ...

R. Pearson Jr.; C. J. Weaver

1989-07-01T23:59:59.000Z

136

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

137

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

138

Underground storage of natural gas, liquid hydrocarbons, and...  

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

Underground storage of natural gas, liquid hydrocarbons, and carbon dioxide (Louisiana) Underground storage of natural gas, liquid hydrocarbons, and carbon dioxide (Louisiana)...

139

Biogeochemistry of Isoprenoid Production and Anaerobic Hydrocarbon Biodgeradation.  

E-Print Network (OSTI)

??This dissertation is an exploration of microbial isoprenoid production and destruction by anaerobic hydrocarbon biodegradation. Isoprenoids are methyl-branched hydrocarbons, and include biomarkers from all three… (more)

Dawson, Katherine

2011-01-01T23:59:59.000Z

140

Interannual Variability and Trends of Extratropical Ozone. Part I: Northern Hemisphere  

Science Conference Proceedings (OSTI)

The authors apply principal component analysis (PCA) to the extratropical total column ozone from the combined merged ozone data product and the European Centre for Medium-Range Weather Forecasts assimilated ozone from January 1979 to August ...

Xun Jiang; Steven Pawson; Charles D. Camp; J. Eric Nielsen; Run-Lie Shia; Ting Liao; Varavut Limpasuvan; Yuk L. Yung

2008-10-01T23:59:59.000Z

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

Quality of Total Ozone Measured by the Focused Sun Method Using a Brewer Spectrophotometer  

Science Conference Proceedings (OSTI)

Strong ozone depletions and large natural variations in total ozone have been observed at high latitudes. Accurate measurements of total ozone are important so as not to misinterpret the involved processes and to track correctly the variations. ...

Weine Josefsson

2003-01-01T23:59:59.000Z

142

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.

143

NRC symposium explores links between greenhouse gases, stratospheric ozone  

SciTech Connect

Two important climatic issues stratospheric ozone depletion and greenhouse gas increase and the apparent connection between them led to the holding in March 1988 of a Joint Symposium on Ozone Depletion, Greenhouse Gases and Climate Change. This symposium was primarily concerned with the linkages between ozone depletion and increasing greenhouse gases and with their combined effect in causing climate change to occur on a global scale. The presentations review the current state of knowledge about stratospheric ozone depletion, discuss the probable effect of predicted greenhouse gas increase on future ozone trends, summarize observational data on changing atmospheric chemistry and associated atmospheric temperatures, and describe the continuing effort to model and predict future scenarios of climatic change relative to ozone and greenhouse gases in both the stratosphere and the troposphere.

1989-04-01T23:59:59.000Z

144

The Cost of Crop Damage Caused by Ozone Air Pollution From Motor Vehicles  

E-Print Network (OSTI)

L. (1982). Assessment of crop loss from ozone. Journal of1984). Assessing impacts of ozone on agricultural crops: II.crop yield functions and alternative exposure statistics.

Murphy, James; Delucchi, Mark; McCubbin, Donald; Kim, H.J.

1999-01-01T23:59:59.000Z

145

In-Situ Electrical Studies on Ozone Functionalization of Graphene  

Science Conference Proceedings (OSTI)

It is found that the ozone molecules at 300 K are reversibly physisorbed on the surface of graphene and the physisorption bonding is removed immediately after  ...

146

In situ gasification process for producing product gas enriched in carbon monoxide and hydrogen  

SciTech Connect

The present invention is directed to an in situ coal gasification process wherein the combustion zone within the underground coal bed is fed with air at increasing pressure to increase pressure and temperature in the combustion zone for forcing product gases and water naturally present in the coal bed into the coal bed surrounding the combustion zone. No outflow of combustion products occurs during the build-up of pressure and temperature in the combustion zone. After the coal bed reaches a temperature of about 2000.degree. F and a pressure in the range of about 100-200 psi above pore pressure the airflow is terminated and the outflow of the combustion products from the combustion zone is initiated. The CO.sub.2 containing gaseous products and the water bleed back into the combustion zone to react endothermically with the hot carbon of the combustion zone to produce a burnable gas with a relatively high hydrogen and carbon monoxide content. About 11 to 29 percent of the gas recovered from the combustion zone is carbon monoxide which is considerably better than the 4 to 10 percent carbon monoxide obtained by employing previously known coal gasification techniques.

Capp, John P. (Morgantown, WV); Bissett, Larry A. (Morgantown, WV)

1978-01-01T23:59:59.000Z

147

A survey of carbon monoxide and nitrogen dioxide in indoor ice arenas in Vermont  

Science Conference Proceedings (OSTI)

Because of the history of health problems traceable to the exhaust of ice resurfacing machines, state sanitarians used detector tubes to measure carbon monoxide (CO) and nitrogen dioxide (NO[sub 2]) levels in enclosed ice arenas in Vermont during high school hockey games. Five of eight arenas had average game CO measurements of 30 ppm carbon monoxide or more. Two of the three periods of play had average CO readings in excess of 100 ppm in one arena. Only six arenas had the complete series of nitrogen dioxide measurements. One had an average game NO[sub 2] level of 1.2 ppm. Two had one or more periods of play that averaged in excess of 0.5 ppm. Despite the ample documentation of the hazards of operating combustion-powered resurfacing machines inside enclosed ice arenas, a significant portion of the arenas had undesirable levels of carbon monoxide or nitrogen dioxide. Ice arenas should be routinely monitored for air contaminants. Considerations should be given to the purchase of electric ice resurfacing machines for new arenas and arenas that have air contamination that cannot be resolved with ventilation.

Paulozzi, L.J. (Vermont Health Dept., Burlington, VT (United States)); Spengler, R.F.; Vogt, R.L.; Carney, J.K.

1993-12-01T23:59:59.000Z

148

Process for recovery of liquid hydrocarbons  

SciTech Connect

Methane is recovered as a gas for discharge to a pipeline from a gas stream containing methane and heavier hydrocarbons, principally ethane and propane. Separation is accomplished by condensing the heavier hydrocarbons and distilling the methane therefrom. A liquid product (LPG) comprising the heavier hydrocarbons is subsequently recovered and transferred to storage. Prior to being discharged to a pipeline, the recovered methane gas is compressed and in undergoing compression the gas is heated. The heat content of the gas is employed to reboil the refrigerant in an absorption refrigeration unit. The refrigeration unit is used to cool the LPG prior to its storage.

Millar, J.F.; Cockshott, J.E.

1978-04-11T23:59:59.000Z

149

Ozone, Air Pollution, and Respiratory Health  

E-Print Network (OSTI)

Of the outdoor air pollutants regulated by the Clean Air Act of 1970 (and recently revised in 1990), ozone has been the one pollutant most difficult to control within the federal standards. The known human health effects are all on the respiratory system. At concentrations of ozone which occur during summer air-pollution episodes in many urban metropolitan areas of the United States, a portion of the healthy population is likely to experience symptoms and reversible effects on lung function, particularly if exercising heavily outdoors. More prolonged increase in airway responsiveness and the presence of inflammatory cells and mediators in the airway lining fluid may also result from these naturally occurring exposures. Serial exposures to peak levels of ozone on several consecutive days are more characteristic of pollution episodes in the Northeast United States and may be associated with recurrent symptoms. No "high-risk " or more sensitive group has been found, in contrast to the case of sulfur dioxide, to which asthmatics are more susceptible than normals. The occurrence of multiple exposure episodes within a single year over many years in some areas of California has led to studies looking for chronic effects of ozone exposure on the lung. To date, no conclusive studies have been reported, although further work is under way. Much of what we know about the effects of this gas on the lung are based on controlled exposures to pure gas within an environmental exposure laboratory. Interactions between substances which commonly co-occur in air-pollution episodes are also under investigation.

William S

1991-01-01T23:59:59.000Z

150

Ozone and UV for Grain Milling Systems  

Science Conference Proceedings (OSTI)

Recognizing the current concerns with food safety, First Energy Services and EPRI collaborated in a project to investigate the feasibility of using ozone as a substitute for chlorinated water to control bacteria and mold at the Harvest States Amber Milling facility in Huron, Ohio. Traditionally, chlorinated water is used to control bacteria and mold in grain processing. Since chlorine usage can be costly and because chlorine presents problems in storage and safe handling of chlorine gas, the project part...

2000-12-13T23:59:59.000Z

151

An Assessment of Tropospheric Ozone Pollution  

Science Conference Proceedings (OSTI)

This assessment was prepared as an initiative of the North American Research Strategy for Tropospheric Ozone (NARSTO). The NARSTO partnership is a non-binding, tri-national public/private alliance, open to science agencies, regulatory agencies, regulated industries, academic institutions, environmentalists, and public interests groups in Canada, Mexico, and the United States. The NARSTO mission is to plan, coordinate, and facilitate comprehensive, long-term, policy-relevant scientific research and assess...

2000-09-25T23:59:59.000Z

152

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

E-Print Network (OSTI)

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

Joel S. Levine

1994-01-01T23:59:59.000Z

153

Motor vehicle fuel economy, the forgotten HC control stragegy. [Hydrocarbon (HC)  

DOE Green Energy (OSTI)

Emissions of hydrocarbons from motor vehicles are recognized as major contributors to ozone pollution in urban areas. Petroleum-based motor fuels contain volatile organic compounds (VOC) which, together with oxides of nitrogen, promote the formation of ozone in the troposphere via complex photochemical reactions. VOC emissions from the tailpipe and evaporation from the fuel and engine systems of highway vehicles are believed to account for about 40% of total VOC emissions in any region. But motor fuels also generate emissions throughout the fuel cycle, from crude oil production to refining, storage, transportation, and handling, that can make significant contributions to the total inventory of VOC emissions. Many of these sources of emissions are directly related to the quantity of fuel produced and handled throughout the fuel cycle. It is, therefore, reasonable to expect that a reduction in total fuel throughput might result in a reduction of VOC emissions. In particular, reducing vehicle fuel consumption by increasing vehicle fuel economy should reduce total fuel throughput, thereby cutting total emissions of VOCS. In this report we identify the sources of VOC emissions throughout the motor fuel cycle, quantify them to the extent possible, and describe their dependence on automobile and light truck fuel economy.

Deluchi, M.; Wang, Quanlu; Greene, D.L.

1992-06-01T23:59:59.000Z

154

Stratospheric ozone in the planetary boundary layer  

Science Conference Proceedings (OSTI)

The impact of stratospheric ozone associated with rapid transport processes at remote Whiteface Mountain, New York was studied using /sup 7/Be as a stratospheric tracer. The seasonal variation of /sup 7/Be concentration suggests that the greatest impact of stratospheric ozone at Whiteface Mountain occurs during late spring and early summer consistent with the time when the impact of tropopause folding should be maximum. This is also the time when tropospheric photochemical ozone production is likely to be maximum. The analysis of 33 cases with peak /sup 7/Be > 175 fCi/m/sup 3/ shows strong correlation between averaged O/sub 3/ and /sup 7/Be concentration. Assuming peak /sup 7/Be is associated with rapid transport we estimate 12 ppbv as the 24th average increased O/sub 3/ due to tropopause folding events. Also the average SO/sub 4/2/sup -/ concentration peaked a day after /sup 7/Be suggesting the backside of the weather system responsible for rapid subsidence also favors transport to this site from distant urban-industrial centers. Thus, photochemical pollution episodes may be intensified by stratospheric subsidence.

Dutkiewicz, V.A.; Husain, L.; Rusheed, A.

1980-01-01T23:59:59.000Z

155

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

156

HYDROCARBONS FROM PLANTS: ANALYTICAL METHODS AND OBSERVATIONS  

E-Print Network (OSTI)

W. and Calvin, M. J. Amer. Oil Chern. Assoc. Science,· 208,of the production of oil and alcohol from hydrocarbon-Figure 1 Cumulative U.S. crude oil discoveries as a function

Calvin, Melvin

2013-01-01T23:59:59.000Z

157

Thermodynamic Properties of Acetic Acid + Hydrocarbons ...  

Science Conference Proceedings (OSTI)

Thermodynamic Properties of Acetic Acid + Hydrocarbons Mixtures L. Negadi1,C,S, N. Ainous2, A. Negadi1, I. Mokbel2, A. Kaci3 and J. Jose2 ...

2006-07-20T23:59:59.000Z

158

Process for Photochemical Chlorination of Hydrocarbons  

DOE Patents (OSTI)

A process for chlorination of a major portion of the hydrogen atoms of paraffinic hydrocarbons of five or more carbon atoms may be replaced by subjecting the hydrocarbon to the action of chlorine under active light. The initial chlorination is begun at 25 to 30 deg C with the chlorine diluted with HCl. The later stages may be carried out with undiluted chlorine and the temperature gradually raised to about 129 deg C.

Beanblossom, W.S.

1950-10-31T23:59:59.000Z

159

Formation of hydrocarbons by bacteria and algae  

SciTech Connect

A literature review has been performed summarizing studies on hydrocarbon synthesis by microorganisms. Certain algal and bacterial species produce hydrocarbons in large quantities, 70 to 80% of dry cell mass, when in a controlled environment. The nutritional requirements of these organisms are simple: CO/sub 2/ and mineral salts. The studies were initiated to determine whether or not microorganisms played a role in petroleum formation. 90 references. (DMC)

Tornabene, T.G.

1980-12-01T23:59:59.000Z

160

Clean, economical, underwater (hydrocarbon) storage  

SciTech Connect

A consortium consisting of Howaldtswerke-Deutsche Werft A.G., Phoenix Gummiwerke A.G., Strabag Bau-A.G., and Bugsier Reederei und Bergungs-A.G. offers a plausible solution to the large-scale underwater storage of hydrocarbons. Up to 20 storage compartments of 8000 cu m capacity can be assembled for a capacity of 160,000 cu m. Each compartment is divided in half by a nylon-reinforced polyurethane diaphragm which isolates oil or other products on one side from sea-water ballast on the other side. As oil is pumped into storage on one side of the diaphragm, the diaphragm moves and ballast on the other side is displaced to the sea. Ballast re-enters the compartment during unloading. The system can enable small offshore platforms to produce more economically. Cargo tankers load at 8000 cu m/hr. The tanks will be used in 200 m or greater water depths. The loading station is installed in a buoy 30 m below the water surface.

1978-08-01T23:59:59.000Z

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.


161

Massive global ozone loss predicted following regional nuclear conflict  

E-Print Network (OSTI)

Massive global ozone loss predicted following regional nuclear conflict Michael J. Mills* , Owen B a chemistry-climate model and new estimates of smoke produced by fires in contemporary cities to calculate the impact on stratospheric ozone of a regional nuclear war between developing nuclear states involving 100

162

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

163

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

164

The 1983 and 1985 Anomalies in Ozone Distribution in Perspective  

Science Conference Proceedings (OSTI)

Studies of the amount of total ozone at many observatories show that the negative 1983 deviation from the long-term average exceeded 2?, and was the greatest in magnitude for an annual deviation in their entire record., the total ozone in ...

Rumen D. Bojkov

1987-10-01T23:59:59.000Z

165

Ozonated Laundry: An Analysis of Its Applications and Market Potential  

Science Conference Proceedings (OSTI)

Electric utilities can create value for their customers and revenues for themselves by promoting new energy-intensive technologies. This report focuses on one such electrotechnology, ozonated laundry. It describes the current state of the technology and its economic prospects and explores how utilities can benefit from increased marketplace acceptance of ozonated laundry.

1998-12-23T23:59:59.000Z

166

Autoregressive forecast of monthly total ozone concentration: A neurocomputing approach  

Science Conference Proceedings (OSTI)

The present study endeavors to generate autoregressive neural network (AR-NN) models to forecast the monthly total ozone concentration over Kolkata (22^o34', 88^o22'), India. The issues associated with the applicability of neural network to geophysical ... Keywords: Autoregressive moving average, Autoregressive neural network, Monthly total ozone, Predictive model

Goutami Chattopadhyay; Surajit Chattopadhyay

2009-09-01T23:59:59.000Z

167

An Analysis of Tropopause Pressure and Total Ozone Correlations  

Science Conference Proceedings (OSTI)

The relationship between total ozone and tropopause pressure is analyzed using 4 years (1979–82) of Nimbus-7 total ozone data and NMC global analyses of tropopause on a 5° by 5° grid. The fields are separated into medium (synoptic) and large ...

Siegfried D. Schubert; Marie-Jeanne Munteanu

1988-03-01T23:59:59.000Z

168

SYNTHESIS OF OXYGENATED PRODUCTS FROM CARBON MONOXIDE AND HYDROGEN OVER SILICA- AND ALUMINA-SUPPORTED RUTHENIUM CATALYSTS  

E-Print Network (OSTI)

R. B. , "The Fischer-Tropsch and Related Syntheses", Wiley,with hydrocarbons during Fischer-Tropsch synthesis over iron

Kellner, C.Stephen

2013-01-01T23:59:59.000Z

169

PHASE BEHAVIOR OF LIGHT GASES IN HYDROCARBON AND AQUEOUS SOLVENTS  

Science Conference Proceedings (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 period, the Park-Gasem-Robinson (PGR) equation of state (EOS) has been modified to improve its volumetric and equilibrium predictions. Specifically, the attractive term of the PGR equation was modified to enhance the flexibility of the model, and a new expression was developed for the temperature dependence of the attractive term in this segment-segment interaction model. The predictive capability of the modified PGR EOS for vapor pressure, and saturated liquid and vapor densities was evaluated for selected normal paraffins, normal alkenes, cyclo-paraffins, light aromatics, argon, carbon dioxide and water. The generalized EOS constants and substance-specific characteristic parameters in the modified PGR EOS were obtained from the pure component vapor pressures, and saturated liquid and vapor molar volumes. The calculated phase properties were compared to those of the Peng-Robinson (PR), the simplified-perturbed-hard-chain theory (SPHCT) and the original PGR equations. Generally, the performance of the proposed EOS was better than the PR, SPHCT and original PGR equations in predicting the pure fluid properties (%AAD of 1.3, 2.8 and 3.7 for vapor pressure, saturated liquid and vapor densities, respectively).

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

1998-08-31T23:59:59.000Z

170

An Update through 1985 of the Variations in Global Total Ozone and North Temperate Layer-Mean Ozone  

Science Conference Proceedings (OSTI)

Total-ozone variations in five climatic zones and the world as a whole, as well as ozone variations in tropospheric and stratospheric layers of the north temperate zone, have been updated through 1985 by means of Dobson, ozonesonde and Umkehr ...

J. K. Angell

1988-01-01T23:59:59.000Z

171

Interaction and reactivity of nitric oxide and carbon monoxide on ruthenium surfaces  

DOE Green Energy (OSTI)

A multifaceted investigation of the reduction of nitric oxide by carbon monoxide using a ruthenium (102) single crystal catalyst in the pressure range 10/sup -3/ to 10 Torr and temperature range of 300 to 475/sup 0/C has been undertaken. Kinetic and isotopic results indicate that the reaction products CO/sub 2/ and N/sub 2/ were produced via two reaction mechanisms. Using a reducing gas mixture (low P/sub NO//P/sub CO/ ratio) a two site mechanism was operative involving NO dissociation. The carbon monoxide kinetic order varied from +1 to -3 and the nitric oxide order varied from +1 to 0. The catalyst under these conditions was determined to be metallic ruthenium with oxygen bonded within the first surface layer. The oxygen was unreactive and formed a (1 x 3)-0 LEED pattern. Under oxidizing conditions (high P/sub NO//P/sub CO/ ratio) the catalyst was ruthenium dioxide and the functional mechanism under these reaction conditions yielded a nitric oxide order of +2 to -4. Inclusion of a site poisoning mechanism under reducing conditions and an RuO/sub 2/ growth mechanism involving ruthenium cation transfer under oxidizing conditions into the kinetic rate laws led to an overall rate law which could be fit to the carbon monoxide and nitric oxide order plots. Using isotopically oxygen labelled reactants, it was observed that the three possible isotopes of carbon dioxide were produced. A ..gamma..-CO surface species is postulated as an intermediate in the exchange process. The reaction was observed to be initially surface structure insensitive and the reaction kinetics were derived using a Langmuir-Hinshelwood formalism.

Quick, E.E.

1980-03-01T23:59:59.000Z

172

Syngas Upgrading to Hydrocarbon Fuels Technology Pathway  

SciTech Connect

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

173

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

SciTech Connect

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

174

Ozone depletion, greenhouse gases, and climate change: Proceedings  

SciTech Connect

This symposium was primarily concerned with the linkages between ozone depletion and increasing greenhouse gases and with their combined effect in causing climate change to occur on a global scale. The presentations in these proceedings review the current state of knowledge about stratospheric ozone depletion, discuss the probable effect of predicted greenhouse gas increase on future ozone trends, summarize observational data on changing atmospheric chemistry and associated atmospheric temperatures, and describe the continuing effort to model and predict future scenarios of climatic change relative to ozone and greenhouse gases in both the stratosphere and the troposphere. Some of the questions and answers that followed the presentations have been included when they highlight noteworthy points that were not covered in the presentation itself. The request by the National Climate Program Office for a symposium on the above related issues is included. The symposium agenda and participants are given. As well as a glossary of special terms and abbreviations. In summary, the Joint Symposium on Ozone Depletion, Greenhouse Gases, and Climate Change reviewed the magnitude and causes of stratospheric ozone depletion and examined the connections that exist between this problem and the impending climate warming to increasing greenhouse gases. The presentations of these proceedings indicate that the connections are real and important, and that the stratospheric ozone depletion and tropospheric greenhouse warming problems must be studied as parts of an interactive global system rather than as more or less unconnected events.

1989-01-01T23:59:59.000Z

175

Laboratory Measurement of Secondary Pollutant Yields from Ozone Reaction  

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

Laboratory Measurement of Secondary Pollutant Yields from Ozone Reaction Laboratory Measurement of Secondary Pollutant Yields from Ozone Reaction with HVAC Filters Title Laboratory Measurement of Secondary Pollutant Yields from Ozone Reaction with HVAC Filters Publication Type Conference Proceedings Year of Publication 2009 Authors Destaillats, Hugo, Wenhao Chen, Michael G. Apte, Nuan Li, Michael Spears, Jérémie Almosni, Jianshun Zheng, and William J. Fisk Conference Name Proceedings of the Healthy Buildings 2009 Conference Conference Location Syracuse, NY Keywords building-related symptoms, hvac filter, ozone, ptr-ms, secondary pollutants Abstract We used Proton Transfer Reaction - Mass Spectrometry (PTR-MS) and conventional sampling methods to monitor and identify trace level organic pollutants formed in heterogeneous reactions between ozone and HVAC filters in real time. Experiments were carried out using a bench-scale flow tube reactor operating with dry air and humidified air (50% RH), at realistically high ozone concentrations (150 ppbv). We explored different filter media (i.e., fiberglass and cotton/polyester blends) and different particle loadings (i.e., clean filter and filters loaded with particles for 3 months at the Lawrence Berkeley National Laboratory and the Port of Oakland, CA). Detailed emission dynamics of very low levels of certain organic pollutants from filter media upon ozone exposure in the presence of moisture have been obtained and analyzed.

176

George A. Olah, Carbocation and Hydrocarbon Chemistry  

Office of Scientific and Technical Information (OSTI)

George A. Olah, Carbocation and Hydrocarbon Chemistry George A. Olah, Carbocation and Hydrocarbon Chemistry Resources with Additional Information · Patents George A. Olah Courtesy Rand Larson, Morningstar Productions George Olah received the 1994 Nobel Prize in Chemistry "for his contribution to carbocation chemistry" and his 'role in the chemistry of hydrocarbons. In particular, he developed superacids ... that are much stronger than ordinary acids, are non-nucleophilic, and are fluid at low temperatures. In such media ... carbocations are stable and their physical properties ... can be observed, thus allowing details of their structures to be determined. Besides trivalent ions ... Olah demonstrated the existence of higher coordinate carbocations ... . These species do not violate the octet rule, but involve 2-electron 3-center bonding. '1

177

Gulf Hydrocarbon Inc | Open Energy Information  

Open Energy Info (EERE)

Hydrocarbon Inc Hydrocarbon Inc Jump to: navigation, search Name Gulf Hydrocarbon Inc Address 2016 Main St Place Houston, Texas Zip 77002 Sector Biofuels Product Wholesale marketing of biodiesel and ethanol to refiners, blenders and petroleum distributors Website http://www.gulfhydrocarbon.com Coordinates 29.749227°, -95.371693° Loading map... {"minzoom":false,"mappingservice":"googlemaps3","type":"ROADMAP","zoom":14,"types":["ROADMAP","SATELLITE","HYBRID","TERRAIN"],"geoservice":"google","maxzoom":false,"width":"600px","height":"350px","centre":false,"title":"","label":"","icon":"","visitedicon":"","lines":[],"polygons":[],"circles":[],"rectangles":[],"copycoords":false,"static":false,"wmsoverlay":"","layers":[],"controls":["pan","zoom","type","scale","streetview"],"zoomstyle":"DEFAULT","typestyle":"DEFAULT","autoinfowindows":false,"kml":[],"gkml":[],"fusiontables":[],"resizable":false,"tilt":0,"kmlrezoom":false,"poi":true,"imageoverlays":[],"markercluster":false,"searchmarkers":"","locations":[{"text":"","title":"","link":null,"lat":29.749227,"lon":-95.371693,"alt":0,"address":"","icon":"","group":"","inlineLabel":"","visitedicon":""}]}

178

Sensitivity Analysis of Ozone Formation and Transport for a Central  

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

Sensitivity Analysis of Ozone Formation and Transport for a Central Sensitivity Analysis of Ozone Formation and Transport for a Central California Air Pollution Episode Title Sensitivity Analysis of Ozone Formation and Transport for a Central California Air Pollution Episode Publication Type Journal Article Year of Publication 2008 Authors Jin, Ling, Shaheen R. Tonse, Daniel S. Cohan, Xianglei Mao, Robert A. Harley, and Nancy J. Brown Journal Environmental Science & Technology Volume 42 Start Page 3683 Issue 10 Pagination 3683-3689 Date Published 05/2008 Abstract We developed a first- and second-order sensitivity analysis approach with the decoupled direct method to examine spatial and temporal variations of ozone-limiting reagents and the importance of local vs upwind emission sources in the San Joaquin Valley of central California for a 5 day ozone episode (Jul 29th to Aug 3rd, 2000). Despite considerable spatial variations, nitrogen oxides (NOx) emission reductions are overall more effective than volatile organic compound (VOC) control for attaining the 8 h ozone standard in this region for this episode, in contrast to the VOC control that works better for attaining the prior 1 h ozone standard. Interbasin source contributions of NOx emissions are limited to the northern part of the SJV, while anthropogenic VOC (AVOC) emissions, especially those emitted at night, influence ozone formation in the SJV further downwind. Among model input parameters studied here, uncertainties in emissions of NOx and AVOC, and the rate coefficient of the OH + NO2 termination reaction, have the greatest effect on first-order ozone responses to changes in NOx emissions. Uncertainties in biogenic VOC emissions only have a modest effect because they are generally not collocated with anthropogenic sources in this region.

179

Determination of total ozone from DMSP multichannel filter radiometer measurements  

Science Conference Proceedings (OSTI)

The multichannel filter radiometer (MFR) infrared sensor was first flown in 1977 on a Defense Meteorological Satellite Program (DMSP) Block 5D series satellite operated by the US Air Force. The first four satellites in this series carried MFR sensors from which total atmospheric column ozone amounts may be derived. The last MFR sensor ceased operating on February 16, 1980. The series of four sensors spans a data period of nearly three years. The MFR sensor measures infrared radiances for 16 channels. Total ozone amounts are determined from sets of radiance measurements using an empirical relationship that is developed using linear regression analysis. Total ozone is modeled as a linear combination of terms involving functions of the MFR radiances for four channels (1, 3, 7 and 16) and the secant of the zenith angle. The ozone retrieval methodology is described schematically. The ozone retrieval model is developed through regression analysis using sets of simulated MFR radiances derived from detailed radiative transfer calculations. The MFR total ozone data are compared with independent ground-based Dobson measurements in order to evaluate the ozone retrieval methodology. Many Dobson observatories have been providing their daily measurements of total ozone which are taken close in time to DMSP overpass times. MFR total ozone data are compared with Dobson measurements taken between January 1 and February 15, 1979, and the results are summarized. Comparisons were made where the MFR and Dobson measurements are within 300 km and 300 minutes of each other. Percentages are computed with respect to the Dobson values. The MFR data were processed using a preliminary methodology, and the data will be reprocessed in the near future.

Luther, F.M.; Weichel, R.L.

1980-09-01T23:59:59.000Z

180

Catalysts for synthesizing various short chain hydrocarbons  

DOE Green Energy (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.


181

Effect of ozone on growth and assimilate partitioning in parsley  

SciTech Connect

Parsley (Petroselinum crispum (Mill.) Nym. cv. Banquet) incurred leaf injury, reduced growth, and altered assimilate partitioning after exposures to 20 pphm ozone. Total plant dry weight and root dry weight were decreased 23% and 43% respectively, with little effect on leaves. The relative growth rate of fumigated plants was reduced after the initial ozone exposure but leveled off at a steady state above that of the control plants when plant dry weights reached about 4.5 g. Ozone appeared to have its greatest effect on growth during initial exposures. 15 references, 3 figures, 1 table.

Oshima, R.J.; Bennett, J.P.; Braegelmann, P.K.

1978-05-01T23:59:59.000Z

182

Exposure-Relevant Ozone Chemistry in Occupied Spaces  

SciTech Connect

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

183

Ozone generation by rock fracture: Earthquake early warning?  

Science Conference Proceedings (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

184

A Study on the Planetary Wave Transport of Ozone during the Late February 1979 Stratospheric Warming Using the SAGE Ozone Observation and Meteorological Information  

Science Conference Proceedings (OSTI)

Ozone data from the Stratospheric Aerosol and Gas Experiment (SAGE) have been used in conjunction with meteorological information to study the ozone transport near 55°N due to planetary waves during the late February 1979 stratospheric warming. ...

Pi-Huan Wang; M. P. McCormick; W. P. Chu

1983-10-01T23:59:59.000Z

185

Biogenic Hydrocarbons in the Atmospheric Boundary Layer: A Review  

Science Conference Proceedings (OSTI)

Nonmethane hydrocarbons are ubiquitous trace atmospheric constituents yet they control the oxidation capacity of the atmosphere. Both anthropogenic and biogenic processes contribute to the release of hydrocarbons to the atmosphere. In this ...

J. D. Fuentes; L. Gu; M. Lerdau; R. Atkinson; D. Baldocchi; J. W. Bottenheim; P. Ciccioli; B. Lamb; C. Geron; A. Guenther; T. D. Sharkey; W. Stockwell

2000-07-01T23:59:59.000Z

186

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

SciTech Connect

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

187

Co-cultured Synechococcus and Shewanella Produce Hydrocarbons ...  

... microbes has been developed. These hydrocarbons may be further processed into vehicle fuels using traditional oil refining techniques.

188

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, Edward J. (Havertown, PA); Hollstein, Elmer J. (Wilmington, DE)

1985-12-31T23:59:59.000Z

189

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

190

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

191

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

192

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

193

Method for recovery of hydrocarbon material from hydrocarbon material-bearing formations  

SciTech Connect

A method is disclosed for heating a hydrocarbon material contained in a recovery zone in an underground hydrocarbon material-bearing formation to reduce the viscosity thereof for facilitating recovery of the hydrocarbon material. A gaseous penetration medium comprising a gaseous working fluid and a carrier gas, is fed into the formation at a penetration pressure sufficient for penetration of the recovery zone, the working fluid being a water soluble gas which generates heat of solution upon absorption in an aqueous medium, and in which the partial pressure of the working fluid in relation to the penetration pressure and the temperature prevailing in the recovery zone is controlled to inhibit working fluid condensation but to provide for absorption of working fluid by water present in the formation to release heat for heating the hydrocarbon material in the recovery zone.

Kalina, A.I.

1982-05-25T23:59:59.000Z

194

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

195

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

196

Trace elements and Polycyclic Aromatic Hydrocarbons (PAHs)  

E-Print Network (OSTI)

.2.2 Anthropogenic emissions 28 2.3 Polycyclic Aromatic Hydrocarbons 30 2.3.1 Sources of PAHs 30 2.3.2 Gas to particle distribution in atmosphere 32 2.3.3 Gas to particle distribution in atmosphere 32 CHAPTER THREE

Paris-Sud XI, Université de

197

Sensitivity of Surface Ozone Simulation to Cumulus Parameterization  

Science Conference Proceedings (OSTI)

Different cumulus schemes cause significant discrepancies in simulated precipitation, cloud cover, and temperature, which in turn lead to remarkable differences in simulated biogenic volatile organic compound (BVOC) emissions and surface ozone ...

Zhining Tao; Allen Williams; Ho-Chun Huang; Michael Caughey; Xin-Zhong Liang

2008-05-01T23:59:59.000Z

198

Isentropic Cross-Tropopause Ozone Transport in the Northern Hemisphere  

Science Conference Proceedings (OSTI)

This paper investigates isentropic ozone exchange between the extratropical lower stratosphere and the subtropical upper troposphere in the Northern Hemisphere. The quantification method is based on the potential vorticity (PV) mapping of ...

P. Jing; D. M. Cunnold; H. J. Wang; E-S. Yang

2004-05-01T23:59:59.000Z

199

Indoor Surface Chemistry: Ozone Reaction with Nicotine Sorbed...  

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

Indoor Surface Chemistry: Ozone Reaction with Nicotine Sorbed to Model Materials Speaker(s): Hugo Destaillats Date: May 19, 2005 - 12:00pm Location: Bldg. 90 During this seminar,...

200

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.

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

Total Ozone Determination from the Backscattered Ultraviolet (BUV) Experiment  

Science Conference Proceedings (OSTI)

The algorithm used to derive total ozone from the Nimbus 4 Backscattered Ultraviolet (BUV) experiment is described. A seven-year global data set with more than one million retrievals has been produced and archived using this algorithm. The ...

K. F. Klenk; P. K. Bhartia; V. G. Kaveeshwar; R. D. McPeters; P. M. Smith; A. J. Fleig

1982-11-01T23:59:59.000Z

202

Mesoscale Meteorology and High Ozone in the Northeast United States  

Science Conference Proceedings (OSTI)

This study examines the relationship between mesoscale meteorological conditions and high-ozone days in the northeastern United States. It is proposed that the leeside trough and the sea-breeze front are two mesoscale features that can be ...

Robert S. Gaza

1998-09-01T23:59:59.000Z

203

The Ozone Dilemma: a reference handbook (Contemporary World Issues Series)  

E-Print Network (OSTI)

Dilemma: a reference handbook By David E. Newton Reviewed byDilemma: a reference handbook (Contemporary World IssuesThe Ozone Dilemma: a reference handbook is targeted at both

Li, Haipeng

1997-01-01T23:59:59.000Z

204

An Intercomparison of Ground-Based Total Ozone Instruments  

Science Conference Proceedings (OSTI)

Five ground-based total ozone spectrophotometers were intercompared at Wallops Island, Virginia between October 1979 and January 1981. The tests were conducted to evaluate the stability and accuracy of each instrument over an extended time ...

C. L. Parsons; J. C. Gerlach; M. E. Williams

1982-05-01T23:59:59.000Z

205

Ozone-initiated chemistry in an occupied simulated aircraft cabin  

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

nonanal, decanal, 4-oxopentanal (4-OPA), 6-methyl-5-hepten-2-one (6-MHO), formic acid and acetic acid, with 0.25 to 0.30 moles of quantified product volatilized per mole of ozone...

206

Biofouling Control With Ozone at the Bergen Generating Station  

Science Conference Proceedings (OSTI)

Tests were conducted to evaluate the effectiveness of ozone as an alternative to chlorine for condenser biofouling control in a once-through cooling system. A pilot-scale test facility with three model condensors simulated condenser operation and conditions at the Bergen station. Both ozone and chlorine were tested. The minimum effective level of each was determined by daily measurements of heat transfer coefficients across model condenser tubes and/or water-side pressure drop. Final evaluation was based...

1980-11-01T23:59:59.000Z

207

Probabilistic aspects of meteorological and ozone regional ensemble forecasts  

SciTech Connect

This study investigates whether probabilistic ozone forecasts from an ensemble can be made with skill; i.e., high verification resolution and reliability. Twenty-eight ozone forecasts were generated over the Lower Fraser Valley, British Columbia, Canada, for the 5-day period 11-15 August 2004, and compared with 1-hour averaged measurements of ozone concentrations at five stations. The forecasts were obtained by driving the CMAQ model with four meteorological forecasts and seven emission scenarios: a control run, {+-} 50% NO{sub x}, {+-} 50% VOC, and {+-} 50% NO{sub x} combined with VOC. Probabilistic forecast quality is verified using relative operating characteristic curves, Talagrand diagrams, and a new reliability index. Results show that both meteorology and emission perturbations are needed to have a skillful probabilistic forecast system--the meteorology perturbation is important to capture the ozone temporal and spatial distribution, and the emission perturbation is needed to span the range of ozone-concentration magnitudes. Emission perturbations are more important than meteorology perturbations for capturing the likelihood of high ozone concentrations. Perturbations involving NO{sub x} resulted in a more skillful probabilistic forecast for the episode analyzed, and therefore the 50% perturbation values appears to span much of the emission uncertainty for this case. All of the ensembles analyzed show a high ozone concentration bias in the Talagrand diagrams, even when the biases from the unperturbed emissions forecasts are removed from all ensemble members. This result indicates nonlinearity in the ensemble, which arises from both ozone chemistry and its interaction with input from particular meteorological models.

Monache, L D; Hacker, J; Zhou, Y; Deng, X; Stull, R

2006-03-20T23:59:59.000Z

208

Ozone in the Troposphere and Stratosphere, part 1  

Science Conference Proceedings (OSTI)

This is the first part of a 2-part Conference Publication. This document contains papers presented at the 1992 Quadrennial Ozone Symposium held at the Charlottesville, Virginia, from June 4-13, 1992. The papers cover topics in both Tropospheric and Stratospheric research. These topics include ozone trends and climatology, ground based, aircraft, balloon, rocket and satellite measurements, Arctic and Antarctic research, global and regional modeling, and volcanic effects. Separate abstracts have been prepared for articles from this report.

Hudson, R.D.

1994-04-01T23:59:59.000Z

209

Ozone in the troposphere and stratosphere, part 2  

Science Conference Proceedings (OSTI)

This is the second of a 2-part Conference Publication. This document contains papers presented at the 1992 Quadrennial Ozone Symposium held at Charlottesville, Virginia, from June 4-13, 1992. The papers cover topics in both Tropospheric and Stratospheric research. These topics include ozone trends and climatology, ground based, aircraft, balloon, rocket and satellite measurements, Arctic and Antarctic research, global and regional modeling, and volcanic effects. Separate abstracts have been prepared for articles from this report.

Hudson, R.D.

1994-04-01T23:59:59.000Z

210

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

E-Print Network (OSTI)

environment; Copper-halide 1. Introduction The use of hydrocarbon fuels for generating power for cars for both transportation and residential power systems. PEM fuel cells operate on hydro- gen. However, the infrastructure for hydrogen that will support large markets is decades away. The use of hydro- carbon fuels (e

Dutta, Prabir K.

211

Interannual Variability of the Antarctic Ozone Hole in a GCM. Part I: The Influence of Tropospheric Wave Variability  

Science Conference Proceedings (OSTI)

To study the interannual variability of the Antarctic ozone hole, a physically realistic parameterization of the chemistry responsible for severe polar ozone loss has been included in the GISS GCM. The ensuing ozone hole agrees well with ...

Drew T. Shindell; Sun Wong; David Rind

1997-09-01T23:59:59.000Z

212

Delayed Southern Hemisphere climate change induced by stratospheric ozone recovery, as projected by the CMIP5 models  

Science Conference Proceedings (OSTI)

Stratospheric ozone is expected to recover by the end of this century due to the regulation of ozone depleting substances by the Montreal Protocol. Targeted modeling studies have suggested that the climate response to ozone recovery will greatly ...

Elizabeth A. Barnes; Nicholas W. Barnes; Lorenzo M. Polvani

213

Gold Nanoparticles Supported on Carbon Nitride: Influence of Surface Hydroxyls on Low Temperature Carbon Monoxide Oxidation  

SciTech Connect

This paper reports the synthesis of 2.5 nm gold clusters on the oxygen free and chemically labile support carbon nitride (C3N4). Despite having small particle sizes and high enough water partial pressure these Au/C3N4 catalysts are inactive for the gas phase and liquid phase oxidation of carbon monoxide. The reason for the lack of activity is attributed to the lack of surface OH groups on the C3N4. These OH groups are argued to be responsible for the activation of CO in the oxidation of CO. The importance of basic OH groups explains the well document dependence of support isoelectric point versus catalytic activity.

Singh, Joseph A [ORNL; Dudney, Nancy J [ORNL; Li, Meijun [ORNL; Overbury, Steven {Steve} H [ORNL; Veith, Gabriel M [ORNL

2012-01-01T23:59:59.000Z

214

EXAFS of carbon monoxide oxidation on supported Pt fuel cell electrocatalysts  

Science Conference Proceedings (OSTI)

The potential dependence of the extended X-ray absorption fine structure (EXAFS) obtained at the Pt L{sub III} absorption edge for a carbon supported Pt electrocatalyst exposed to carbon monoxide is presented. The data have been analyzed using the difference file method to separate the dominant contributions of the Pt neighbors from contributions to the EXAFS from the adsorbed species. The presence of adsorbed CO is clearly observed with a Pt-C distance of 1.85 {angstrom} at potentials less than 0.5 V vs. RHE. Increasing the potential above 0.5 V resulted first in the removal of the adsorbed CO and at more positive potentials, e.g., 1.05 V, in the formation of an oxide layer, as evidenced by the presence of a Pt-O coordination shell at 2.00 {angstrom}. These results demonstrate that in situ EXAFS of supported Pt electrocatalysts may be used to probe adsorbate structures.

Maniguet, S.; Mathew, R.J.; Russell, A.E.

2000-03-09T23:59:59.000Z

215

Role of carboxydobacteria in consumption of atmospheric carbon monoxide by soil  

Science Conference Proceedings (OSTI)

The carbon monoxide consumption rates of the carboxydobacteria Pseudomonas (Seliberia) carboxydohydrogena, P. carboxydovorans, and P. carboxydoflava were measured at high (50%) and low (0.5 ..mu..l liter/sup -1/) mixing ratios of CO in air. CO was only consumed when the bacteria had been grown under CO-autotrophic conditions. At low cell densities the CO comsumption rates measured at low CO mixing ratios were similar in cell suspensions and in mixtures of bacteria in soil. CO consumption observed in natural soil (loess, eolian sand, chernozem) as well as in suspensions or soil mixtures of carboxydobacteria showed Michaelis-Menten kinetics. Considering the difference of the K/sub m/, values and the observed V/sub max/ values, carboxydobacteria cannot contribute significantly to the consumption of atmospheric CO.

Conrad, R. (Max-Planck-Institut fuer Chemie, Mainz, Germany); Meyer, O.; Seiler, W.

1981-08-01T23:59:59.000Z

216

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

217

Ozone observations and a model of marine boundary layer photochemistry during SAGA 3  

SciTech Connect

A major purpose of the third joint Soviet-American Gases and Aerosols (SAGA 3) oceanographic cruise was to examine remote tropical marine O{sub 3} and photochemical cycles in detail. On leg 1, which took place between Hilo, Hawaii, and Pago-Pago, American Samoa, in February and March 1990, shipboard measurements were made of O{sub 3}, CO, CH{sub 4}, nonmethane hydrocarbons (NMHC), NO, dimethyl sulfide (DMS), H{sub 2}S, H{sub 2}O{sub 2}, organic peroxides, and total column O{sub 3}. Postcruise analysis was performed for alkyl nitrates and a set of nonmethane hydrocarbons. A latitudinal gradient in O{sub 3} was observed on SAGA 3, with O{sub 3} north of the intertropical convergence zone (ITCZ) at 15-20 parts per billion by volume (ppbv) and less than 12 ppbv south of the ITCZ but never {le} 3 ppbv as observed on some previous equatorial Pacific cruises. Total column O{sub 3} (230--250 Dobson units (DU)) measured from the Akademik Korolev was within 8% of the corresponding total ozone mapping spectrometer (TOMS) satellite observations and confirmed the equatorial Pacific as a low O{sub 3} region. A one-dimensional photochemical model gives a self-consistent picture of O{sub 3}-NO-CO-hydrocarbon interactions taking place during SAGA 3. At typical equatorial conditions, mean O{sub 3} is 10 ppbv with a 10-15% diurnal variation and maximum near sunrise. Measurements of O{sub 3}, CO, CH{sub 4}, NMHC, and H{sub 2}O constrain model-calculated OH to 9 x 10{sup 5} cm{sup {minus}3} for 10 ppbv O{sub 3} at the equator. The concentrations of alkyl nitrates on SAGA 3 (5-15 pptv total alkyl nitrates) were up to 6 times higher than expected from currently accepted kinetics, suggesting a largely continental source for these species. However, maxima in isopropyl nitrate and bromoform near the equator as well as for nitric oxide may signify photochemical and biological sources of these species. 43 refs., 11 figs., 6 tabs.

Thompson, A.M. [NASA Goddard Space Flight Center, Greenbelt, MD (United States); Johnson, J.E.; Bates, T.S.; Kelly, K.C. [NOAA Pacific Marine Environmental Lab., Seattle, WA (United States); Torres, A.L. [NASA Goddard Space Flight Center, Wallops Island, VA (United States); Atlas, E.; Greenberg, J.P. [National Center for Atmospheric Research (NCAR), Boulder, CO (United States); Donahue, N.M. [Massachusetts Institute of Technology, Cambridge, MA (United States); Yvon, S.A.; Saltzman, E.S. [Univ. of Miami, FL (United States)] [and others

1993-09-20T23:59:59.000Z

218

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

219

ADVANCED OXIDATION: OXALATE DECOMPOSITION TESTING WITH OZONE  

SciTech Connect

At the Savannah River Site (SRS), oxalic acid is currently considered the preferred agent for chemically cleaning the large underground Liquid Radioactive Waste Tanks. It is applied only in the final stages of emptying a tank when generally less than 5,000 kg of waste solids remain, and slurrying based removal methods are no-longer effective. The use of oxalic acid is preferred because of its combined dissolution and chelating properties, as well as the fact that corrosion to the carbon steel tank walls can be controlled. Although oxalic acid is the preferred agent, there are significant potential downstream impacts. Impacts include: (1) Degraded evaporator operation; (2) Resultant oxalate precipitates taking away critically needed operating volume; and (3) Eventual creation of significant volumes of additional feed to salt processing. As an alternative to dealing with the downstream impacts, oxalate decomposition using variations of ozone based Advanced Oxidation Process (AOP) were investigated. In general AOPs use ozone or peroxide and a catalyst to create hydroxyl radicals. Hydroxyl radicals have among the highest oxidation potentials, and are commonly used to decompose organics. Although oxalate is considered among the most difficult organic to decompose, the ability of hydroxyl radicals to decompose oxalate is considered to be well demonstrated. In addition, as AOPs are considered to be 'green' their use enables any net chemical additions to the waste to be minimized. In order to test the ability to decompose the oxalate and determine the decomposition rates, a test rig was designed, where 10 vol% ozone would be educted into a spent oxalic acid decomposition loop, with the loop maintained at 70 C and recirculated at 40L/min. Each of the spent oxalic acid streams would be created from three oxalic acid strikes of an F-area simulant (i.e., Purex = high Fe/Al concentration) and H-area simulant (i.e., H area modified Purex = high Al/Fe concentration) after nearing dissolution equilibrium, and then decomposed to {le} 100 Parts per Million (ppm) oxalate. Since AOP technology largely originated on using ultraviolet (UV) light as a primary catalyst, decomposition of the spent oxalic acid, well exposed to a medium pressure mercury vapor light was considered the benchmark. However, with multi-valent metals already contained in the feed, and maintenance of the UV light a concern; testing was conducted to evaluate the impact from removing the UV light. Using current AOP terminology, the test without the UV light would likely be considered an ozone based, dark, ferrioxalate type, decomposition process. Specifically, as part of the testing, the impacts from the following were investigated: (1) Importance of the UV light on the decomposition rates when decomposing 1 wt% spent oxalic acid; (2) Impact of increasing the oxalic acid strength from 1 to 2.5 wt% on the decomposition rates; and (3) For F-area testing, the advantage of increasing the spent oxalic acid flowrate from 40 L/min (liters/minute) to 50 L/min during decomposition of the 2.5 wt% spent oxalic acid. The results showed that removal of the UV light (from 1 wt% testing) slowed the decomposition rates in both the F & H testing. Specifically, for F-Area Strike 1, the time increased from about 6 hours to 8 hours. In H-Area, the impact was not as significant, with the time required for Strike 1 to be decomposed to less than 100 ppm increasing slightly, from 5.4 to 6.4 hours. For the spent 2.5 wt% oxalic acid decomposition tests (all) without the UV light, the F-area decompositions required approx. 10 to 13 hours, while the corresponding required H-Area decompositions times ranged from 10 to 21 hours. For the 2.5 wt% F-Area sludge, the increased availability of iron likely caused the increased decomposition rates compared to the 1 wt% oxalic acid based tests. In addition, for the F-testing, increasing the recirculation flow rates from 40 liter/minute to 50 liter/minute resulted in an increased decomposition rate, suggesting a better use of ozone.

Ketusky, E.; Subramanian, K.

2012-02-29T23:59:59.000Z

220

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

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

Chemical kinetic modelling of hydrocarbon ignition  

DOE Green Energy (OSTI)

Chemical kinetic modeling of hydrocarbon ignition is discussed with reference to a range of experimental configurations, including shock tubes, detonations, pulse combustors, static reactors, stirred reactors and internal combustion engines. Important conditions of temperature, pressure or other factors are examined to determine the main chemical reaction sequences responsible for chain branching and ignition, and kinetic factors which can alter the rate of ignition are identified. Hydrocarbon ignition usually involves complex interactions between physical and chemical factors, and it therefore is a suitable and often productive subject for computer simulations. In most of the studies to be discussed below, the focus of the attention is placed on the chemical features of the system. The other physical parts of each application are generally included in the form of initial or boundary conditions to the chemical kinetic parts of the problem, as appropriate for each type of application being addressed.

Westbrook, C.K.; Pitz, W.J.; Curran, H.J.; Gaffuri, P.; Marinov, N.M.

1995-08-25T23:59:59.000Z

222

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

223

HYDROCARBON FORMATION ON POLYMER-SUPPORTED COBALT  

SciTech Connect

In this report we detail the synthesis catalytic chemistry of polystyrene supported {eta}{sup 5} ~cyclopentadienyl- dicarbonyl cobalt, CpCo(CO){sub 2}. This material is active in the hydrogenation of CO to saturated linear hydrocarbons and appears to retain its "homogeneous", mononuclear character during the course of its catalysis, During ·the course of our work 18% and 20% crosslinked analogs of polystyrene supported CpCo(CO){sub 2} were shown to exhibit limited catalytic activity and no CO activation.

Benner, Linda S.; Perkins, Patrick; Vollhardt, K.Peter C.

1980-10-01T23:59:59.000Z

224

A Review of World Hydrocarbon Resource Assessments  

Science Conference Proceedings (OSTI)

This study reviews assessments of world oil, natural gas, and oil shale resources made between the end of World War II and the end of 1980. Details are provided on the methods used in developing these assessments, geographic coverage, time horizons, and major assumptions (e.g., about discovery rates and recovery factor). Conclusions on the current state of knowledge concerning each of these hydrocarbon resources are presented.

1982-11-01T23:59:59.000Z

225

Literature Review of Background Polycyclic Aromatic Hydrocarbons  

Science Conference Proceedings (OSTI)

Polycyclic aromatic hydrocarbons (PAHs) continuously move through the environment, often via atmospheric transport. The subsequent deposition of particulates containing PAHs along with other sources of PAHs, such as natural vegetative decay, result in "background" PAHs in surficial soils. Even in pristine areas, surface and near surface soils can contain detectable levels of PAHs. This study provides data on the concentrations and distributions of background PAHs observed in environmental media. Such inf...

2000-03-20T23:59:59.000Z

226

Hydrocarbon content of geopressured brines. Final report  

DOE Green Energy (OSTI)

Design Well data (bottomhole pressure minus wellhead pressure, GWR, and hydrocarbon composition) is presented as a function of producing conditions. These are examined in conjunction with the following models to attempt to deduce the reservoir brine saturation level: (1) reservoir contains gas dispersed in the pores and the gas saturation is greater than critical; (2) reservoir brine is gas-saturated; (3) bubble point below hydrostatic pressure; and (4) bubble point between hydrostatic pressure and reservoir pressure. 24 figs., 10 tabs. (ACR)

Osif, T.L.

1985-08-01T23:59:59.000Z

227

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.

Hsu, Wen L. (Danville, CA)

1989-01-01T23:59:59.000Z

228

Impact of Surfaces on Ozone-Terpene Conversion Rates in Buildings  

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

Impact of Surfaces on Ozone-Terpene Conversion Rates in Buildings Speaker(s): Glenn Morrison Date: March 5, 2007 - 4:00pm Location: 90-3122 Indoor surface reactions of ozone with...

229

Transport, Radiative, and Dynamical Effects of the Antarctic Ozone Hole: A GFDL “SKYHI” Model Experiment  

Science Conference Proceedings (OSTI)

The GFDL “SKYHI” general circulation model has been used to simulate the effect of the Antarctic “ozone hole” phenomenon on the radiative and dynamical environment of the lower stratosphere. Both the polar ozone destruction and photochemical ...

J. D. Mahlman; L. J. Umscheid; J. P. Pinto

1994-02-01T23:59:59.000Z

230

Climate Change and the Middle Atmosphere. Part IV: Ozone Response to Doubled CO2  

Science Conference Proceedings (OSTI)

Parameterized stratospheric ozone photochemistry has been included in the Goddard Institute for Space Studies (GISS) GCM to investigate the coupling between chemistry and climate change for the doubled CO2 climate. The chemical ozone response is ...

Drew T. Shindell; David Rind; Patrick Lonergan

1998-05-01T23:59:59.000Z

231

Global Ozone Observations from the UARS MLS: An Overview of Zonal-Mean Results  

Science Conference Proceedings (OSTI)

Global ozone observations from the Microwave Limb Sounder (MLS) aboard the Upper Atmosphere Research Satellite (UARS) are presented, in both vertically resolved and column abundance formats. The authors review the zonal-mean ozone variations ...

Lucien Froidevaux; Joe W. Waters; William G. Read; Lee S. Elson; Dennis A. Flower; Robert F. Jarnot

1994-10-01T23:59:59.000Z

232

Isolation of the Ozone QBO in SAGE II Data by Singular-Value Decomposition  

Science Conference Proceedings (OSTI)

Detailed structure of the global quasi-biennial oscillation (QBO) in ozone is analyzed using Stratospheric Aerosol and Gas Experiment II ozone and nitrogen dioxide data. Emphasis is placed on the midlatitude QBO, in particular its vertical ...

William J. Randel; Fei Wu

1996-09-01T23:59:59.000Z

233

On the Role of Ozone in the Stability of Rossby Normal Modes  

Science Conference Proceedings (OSTI)

The role of ozone in the linear stability of Rossby normal modes is examined in a continuously stratified, extratropical baroclinic atmosphere. The flow is described by coupled equations for the quasi-geostrophic potential vorticity and ozone ...

Terrence R. Nathan

1989-07-01T23:59:59.000Z

234

A Process-Analysis Based Study of the Ozone Weekend Effect  

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

A Process-Analysis Based Study of the Ozone Weekend Effect Title A Process-Analysis Based Study of the Ozone Weekend Effect Publication Type Journal Article Year of Publication...

235

Predicting Total Ozone Based on GTS Data: Applications for South American High-Latitude Populations  

Science Conference Proceedings (OSTI)

A regular occurrence during the 1990s has been the excursion of the edge of the springtime Antarctic ozone hole over the southernmost region of the South American continent. Given the essential role of atmospheric ozone in absorbing incoming ...

Anna E. Jones; Tanya Bowden; John Turner

1998-05-01T23:59:59.000Z

236

Stratospheric Temperature and Radiative Forcing Response to 11-Year Solar Cycle Changes in Irradiance and Ozone  

Science Conference Proceedings (OSTI)

The 11-yr solar cycle temperature response to spectrally resolved solar irradiance changes and associated ozone changes is calculated using a fixed dynamical heating (FDH) model. Imposed ozone changes are from satellite observations, in contrast ...

L. J. Gray; S. T. Rumbold; K. P. Shine

2009-08-01T23:59:59.000Z

237

Tobacco smoke aging in the presence of ozone: a room-sized chamber...  

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

Tobacco smoke aging in the presence of ozone: a room-sized chamber study Title Tobacco smoke aging in the presence of ozone: a room-sized chamber study Publication Type Journal...

238

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.

239

Association of the Laminated Vertical Ozone Structure with the Lower-Stratospheric Circulation  

Science Conference Proceedings (OSTI)

In this study the examination of the role of the atmospheric circulation in the lower stratosphere in relation to the laminated structure of ozone in the subtropical atmosphere is attempted. This analysis is based on the vertical ozone profile ...

C. Varotsos; P. Kalabokas; G. Chronopoulos

1994-04-01T23:59:59.000Z

240

Total Ozone Variations 1970-74 Using Backscattered Ultraviolet (BUV) and Ground-Based Observations  

Science Conference Proceedings (OSTI)

The most long-lived satellite set of ozone observations, to date, is that derived from the Backscatter Ultraviolet (BUV) ozone sensor on Nimbus 4 and extends from April 1970 through 1976. Unfortunately, this experiment suffered spacecraft power ...

A. J. Miller; R. M. Nagatani; T. G. Rogers; A. J. Fleig; D. F. Heath

1982-05-01T23:59:59.000Z

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.


241

Wintertime Ozone Fluxes and Profiles above a Subalpine Spruce–Fir Forest  

Science Conference Proceedings (OSTI)

High rural concentrations of ozone (O3) are thought to be stratospheric in origin, advected from upwind urban sources, or photochemically generated locally by natural trace gas emissions. Ozone is known to be transported vertically downward from ...

Karl Zeller

2000-01-01T23:59:59.000Z

242

The Role of Vertical Mixing in the Temporal Evolution of Ground-Level Ozone Concentrations  

Science Conference Proceedings (OSTI)

Aircraft measurements taken during the North American Research Strategy for Tropospheric Ozone-Northeast field study reveal the presence of ozone concentration levels in excess of 80 ppb on a regional scale in the nocturnal residual layer during ...

Jian Zhang; S. Trivikrama Rao

1999-12-01T23:59:59.000Z

243

IMPROVING ANTARCTIC TOTAL OZONE PROJECTIONS BY A PROCESS-ORIENTED MULTIPLE DIAGNOSTIC ENSEMBLE REGRESSION  

Science Conference Proceedings (OSTI)

Accurate projections of stratospheric ozone are required, because ozone changes impact on exposures to ultraviolet radiation and on tropospheric climate. Unweighted multi-model ensemble mean (uMMM) projections from chemistry-climate models (CCMs) ...

Alexey Yu. Karpechko; Douglas Maraun; Veronika Eyring

244

Interannual Variations of Total Ozone at Northern Midlatitudes Correlated with Stratospheric EP Flux and Potential Vorticity  

Science Conference Proceedings (OSTI)

At northern midlatitudes over the 1979–2002 time period, column ozone trends are observed to have maximum negative amplitudes in February and March. Here, the portion of the observed ozone interannual variability and trends during these months ...

L. L. Hood; B. E. Soukharev

2005-10-01T23:59:59.000Z

245

Reconstruction and Simulation of Stratospheric Ozone Distributions during the 2002 Austral Winter  

Science Conference Proceedings (OSTI)

Satellite-based solar occultation measurements during the 2002 austral winter have been used to reconstruct global, three-dimensional ozone distributions. The reconstruction method uses correlations between potential vorticity and ozone to derive ...

C. E. Randall; G. L. Manney; D. R. Allen; R. M. Bevilacqua; J. Hornstein; C. Trepte; W. Lahoz; J. Ajtic; G. Bodeker

2005-03-01T23:59:59.000Z

246

Ozone reduces crop yields and alters competition with weeds such as yellow nutsedge  

E-Print Network (OSTI)

DT (eds. ). Assessment of Crop Loss from Air Pollutants:Ambient ozone and adverse crop re- sponse: An evaluation ofthe effects of ozone on crops and trees. In: Lefohn AS (

Grantz, David A.; Shrestha, Anil

2005-01-01T23:59:59.000Z

247

Longitude-Dependent Decadal Changes of Total Ozone in Boreal Winter Months during 1979–92  

Science Conference Proceedings (OSTI)

A statistical analysis shows that the decadal change of zonally asymmetric total ozone (Total Ozone Mapping Spectrometer data) has a distinct spatial similarity with the decadal change of the 300-hPa geopotential patterns during December–February ...

Dieter Peters; Günter Entzian

1999-04-01T23:59:59.000Z

248

Hydrocarbon Fouling of SCR during PCCI combustion  

SciTech Connect

The combination of advanced combustion with advanced selective catalytic reduction (SCR) catalyst formulations was studied in the work presented here to determine the impact of the unique hydrocarbon (HC) emissions from premixed charge compression ignition (PCCI) combustion on SCR performance. Catalyst core samples cut from full size commercial Fe- and Cu-zeolite SCR catalysts were exposed to a slipstream of raw engine exhaust from a 1.9-liter 4-cylinder diesel engine operating in conventional and PCCI combustion modes. The zeolites which form the basis of these catalysts are different with the Cu-based catalyst made on a chabazite zeolite which las smaller pore structures relative to the Fe-based catalyst. Subsequent to exposure, bench flow reactor characterization of performance and hydrocarbon release and oxidation enabled evaluation of overall impacts from the engine exhaust. The Fe-zeolite NOX conversion efficiency was significantly degraded, especially at low temperatures (<250 C), after the catalyst was exposed to the raw engine exhaust. The degradation of the Fe-zeolite performance was similar for both combustion modes. The Cu-zeolite showed better tolerance to HC fouling at low temperatures compared to the Fe-zeolite but PCCI exhaust had a more significant impact than the exhaust from conventional combustion on the NOX conversion efficiency. Furthermore, chemical analysis of the hydrocarbons trapped on the SCR cores was conducted to better determine chemistry specific effects.

Prikhodko, Vitaly Y [ORNL; Pihl, Josh A [ORNL; Lewis Sr, Samuel Arthur [ORNL; Parks, II, James E [ORNL

2012-01-01T23:59:59.000Z

249

Phase Behavior of Light Gases in Hydrocarbon and Aqueous Solvents  

Science Conference Proceedings (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

250

The Use of Ozone as an Antimicrobial Agent: Agricultural and Food Processing Technical Assessment  

Science Conference Proceedings (OSTI)

Ozone treatment, a highly effective disinfectant long used in Europe, deactivates even the most stubborn organisms. Food processors can use ozone to disinfect raw fruits and vegetables during processing or to disinfect water used for washing foods and food plant equipment. Food researchers and regulators have confirmed ozone as safe. In 1997, EPRI convened an expert panel that submitted a Generally Recognized as Safe (GRAS) affirmation of ozone in food applications to the U.S. Food and Drug Administratio...

2001-11-08T23:59:59.000Z

251

Demonstration of an Ozone System at a Hospital Laundry Facility: Long Beach Medical Center  

Science Conference Proceedings (OSTI)

In its role as a powerful oxidant and biocide, ozone works in the context of laundry facilities to boost the cleaning activity of the various chemicals and chemical compounds. To be used in laundry operations, ozone must be introduced into the wash water via one of the ozone laundry systems available on the market today. This report highlights and quantifies the benefits of an ozone laundry system at the 134-bed Long Beach Medical Center (LBMC) in Long Beach, New York.

2007-08-31T23:59:59.000Z

252

Development of an ozone climatology for Harris County, Texas  

SciTech Connect

The Houston Regional Monitoring Corporation (HRM) has performed continuous ambient air quality and meteorological monitoring in the Ship Channel area of east Harris County since August 1981. The HRM monitoring network is one of the largest Environmental Protection Agency (EPA) approved Prevention of Significant Deterioration (PSD) monitoring network in the United States operated by an industrial group. As an adjunct to its monitoring. HRM has funded extensive meteorological and statistical analyses of ozone monitoring data in Harris County. One of the goals of these studies was to determine those meteorological conditions responsible for the formation of elevated ozone concentrations in Harris County. The analyses performed included the use of principal component analysis and cluster analysis. These analysis techniques have individually been applied to ozone and air quality research problems. The combined use of these techniques in this analysis, however, is a unique application of these statistical tools to an ozone air quality analysis. As a result of these analyses, a climatology of those episodes conducive to elevated ozone formation in Harris County was developed.

Balentine, H.W.; Carter, J.C. (Radian Corp., Austin, TX (USA)); Preston, J. (Tenneco Polymers, Houston, TX (US))

1987-01-01T23:59:59.000Z

253

Operations Evaluation Report -- Pressurized Ozonation System, North Mississippi Medical Center Laundry Operations  

Science Conference Proceedings (OSTI)

This report describes ozone and its benefits in healthcare laundry operations. In particular, case studies of two ozone applications -- one in a 650-bed regional medical center and another in a 131-bed skilled nursing and rehabilitation facility -- highlight and quantify ozone's benefits.

2005-03-22T23:59:59.000Z

254

Retrieval of Tropospheric Carbon Monoxide Profiles from High-Resolution Interferometer Observations: A New Digital Gas Correlation (DGC)Method and Applications  

Science Conference Proceedings (OSTI)

Global tropospheric carbon monoxide (CO) distributions can be retrieved from observations by spaceborne gas correlation radiometers and high-resolution interferometers. The Measurement of Pollution in the Troposphere (MOPITT) is a gas correlation ...

Jinxue Wang; John C. Gille; Paul L. Bailey; Liwen Pan; David Edwards; James R. Drummond

1999-01-01T23:59:59.000Z

255

Methods of Reforming Hydrocarbon Fuels Using Hexaaluminate Catalysts  

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

of Reforming Hydrocarbon Fuels Using of Reforming Hydrocarbon Fuels Using Hexaaluminate Catalysts Contact NETL Technology Transfer Group techtransfer@netl.doe.gov May 2012 Opportunity Research is currently active on the technology "Methods of Reforming Hydrocarbon Fuels Using Hexaaluminate Catalysts." The technology is available for licensing and/or further collaborative research from the U.S. Department of Energy's National Energy Technology Laboratory. Overview This invention discloses a method to reform hydrocarbon fuels using hexa- aluminate catalysts. In general, the method successfully disrupts the forma- tion of carbon that leads to the deactivation of the catalyst, a key element in the reforming of hydrocarbon fuels. When researchers are designing catalysts to reform hydrocarbon fuels, one

256

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

257

Harvester ants utilize cuticular hydrocarbons in nestmate recognition  

E-Print Network (OSTI)

Abstract—Cuticular hydrocarbons appear to play a role in ant nestmate recognition, but few studies have tested this hypothesis experimentally with purified hydrocarbon extracts. We exposed captive colonies of the harvester ant Pogonomyrmex barbatus to small glass blocks coated with whole cuticular lipid extracts and the purified hydrocarbon portion of extracts from nestmate and nonnestmate workers. As an estimate of agonistic behavior, we measured the proportion of ants in contact with blocks that flared their mandibles. Blocks coated with cuticular extracts from nonnestmates were contacted by more workers in one of two experiments and elicited higher levels of aggression in both experiments than blocks bearing extracts from nestmates. The cuticular hydrocarbon fraction of extracts alone was sufficient to elicit agonistic behavior toward nonnestmates. The results demonstrate that harvester ants can perceive differences in cuticular hydrocarbon composition, and can use those differences in nestmate recognition. Key Words—Cuticular hydrocarbons, Formicidae, Nestmate recognition, Pogonomyrmex barbatus.

Diane Wagner; Madeleine Tissot; William Cuevas; Deborah M. Gordon

2000-01-01T23:59:59.000Z

258

Secondary pollutants from ozone reactions with ventilation filters and  

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

Secondary pollutants from ozone reactions with ventilation filters and Secondary pollutants from ozone reactions with ventilation filters and degradation of filter media additives Title Secondary pollutants from ozone reactions with ventilation filters and degradation of filter media additives Publication Type Journal Article Year of Publication 2011 Authors Destaillats, Hugo, Wenhao Chen, Michael G. Apte, Nuan Li, Michael Spears, Jérémie Almosni, Gregory Brunner, Jianshun(Jensen) Zhang, and William J. Fisk Journal Atmospheric Environment Volume 45 Start Page 3561 Issue 21 Pagination 3561-3568 Keywords commercial building ventilation & indoor environmental quality group, commercial building ventilation and indoor environmental quality group, energy analysis and environmental impacts department, indoor environment department, indoor environment group

259

Investigation of formaldehyde and acetaldehyde sampling rate and ozone  

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

Investigation of formaldehyde and acetaldehyde sampling rate and ozone Investigation of formaldehyde and acetaldehyde sampling rate and ozone interference for passive deployment of Waters Sep-Pak XPoSure samplers Title Investigation of formaldehyde and acetaldehyde sampling rate and ozone interference for passive deployment of Waters Sep-Pak XPoSure samplers Publication Type Journal Article Year of Publication 2013 Authors Mullen, Nasim A., Marion L. Russell, Melissa M. Lunden, and Brett C. Singer Journal Atmospheric Environment Volume 80 Pagination 184-189 Date Published 12/2013 Keywords aldehyde; exposure; indoor air quality; passive sampler; residential Abstract This study investigated formaldehyde and acetaldehyde passive sampling rates and ozone interference for the DNPH-based Waters Sep-Pak XPoSure sampler. Previous studies have shown that ozone interferes with active sampling by this cartridge. Our study included one laboratory and six field experiments conducted in Northern California homes. Passive sampling rates of 1.10 ± 0.09 and 0.86 ± 0.10 mL/min determined for formaldehyde and acetaldehyde are lower than previously reported. In a controlled laboratory experiment there were small, statistically insignificant impacts of subsequent ozone exposure on formaldehyde and acetaldehyde mass passively collected on the samplers. This sampler is inexpensive, easy to deploy and to transport by mail, and has a high sampling capacity when used passively; it is suitable for a wide-range of monitoring applications. However, the passive sampling rate remains in question given the internally consistent, but different results obtained in our study and the previous study.

260

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

Science Conference Proceedings (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

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

Catalytic conversion of cellulose to liquid hydrocarbon fuels ...  

Catalytic conversion of cellulose to liquid hydrocarbon fuels by progressive removal of oxygen to facilitate separation processes and achieve high selectivities

262

Novel catalyst for selective NOx reduction using hydrocarbons ...  

This invention discloses a catalyst and process for removing nitrogen oxides from exhaust streams under lean burn conditions using hydrocarbons as the reductant.

263

ORGANIC GEOCHEMICAL STUDIES. I. MOLECULAR CRITERIA FOR HYDROCARBON GENESIS  

E-Print Network (OSTI)

isoprenoid hydrocarbons in crude oils and sediments must beisomers (up to C ) in crude oil and those characterised inarc found ubiqubtously in crude oils and shalt extracts as

McCarthy, Eugene D.; Calvin, Kevin

2008-01-01T23:59:59.000Z

264

Methods for natural gas and heavy hydrocarbon co-conversion  

DOE Patents (OSTI)

A reactor for reactive co-conversion of heavy hydrocarbons and hydrocarbon gases and includes a dielectric barrier discharge plasma cell having a pair of electrodes separated by a dielectric material and passageway therebetween. An inlet is provided for feeding heavy hydrocarbons and other reactive materials to the passageway of the discharge plasma cell, and an outlet is provided for discharging reaction products from the reactor. A packed bed catalyst may optionally be used in the reactor to increase efficiency of conversion. The reactor can be modified to allow use of a variety of light sources for providing ultraviolet light within the discharge plasma cell. Methods for upgrading heavy hydrocarbons are also disclosed.

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

2009-02-24T23:59:59.000Z

265

Recovery of nitrogen and light hydrocarbons from polyalkene ...  

Recovery of nitrogen and light hydrocarbons from polyalkene purge gas United States Patent. Patent Number: 6,576,043: Issued: June 10, 2003: Official Filing:

266

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

267

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

268

Multi-step catalytic hydroprocessing to produce hydrocarbon fuels ...  

Multi-step catalytic hydroprocessing to produce hydrocarbon fuels from biomass pyrolysis bio-oil (PNNL IPID 16665) Pacific Northwest National Laboratory

269

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

270

Polycyclic Aromatic Hydrocarbon Exposure in German Coke Oven Workers.  

E-Print Network (OSTI)

??Polycyclic aromatic hydrocarbons (PAHs) are formed whenever there is incomplete combustion of carbonaceous material. They are ubiquitous in the environment and background levels are found… (more)

Thoroman, Jeffrey S.

2010-01-01T23:59:59.000Z

271

Analysis, anaerobic treatment and ozonation of wool scouring wastewater  

SciTech Connect

Wool scouring effluents (WSE) were analyzed by high-resolution gas chromatography-mass spectrometry (HRGC-MS), and then exposed to anaerobic biological treatment using laboratory scale fixed-bed filters. This resulted in a nearly 50% reduction in chemical oxygen demand (COD). Ozonation of the effluent from the biological step led to an even further decrease in total organic carbon (TOC). The fatty acid content of the WSE was affected by both biological treatment and ozonation. Finally, steroids in the WSE underwent reduction reactions when exposed to the anaerobic biological treatment.

Monteverdi, A.; Rindone, B.; Sorlini, C. (Univ. di Milano (Italy)); Andreoni, V. (Univ. di Torino (Italy)); Rozzi, A. (Inst. di Ingegneria Sanitaria del Politechnico di Milano (Italy))

1992-01-01T23:59:59.000Z

272

Scale-up and Demonstration of Fly Ash Ozonation Technology  

Science Conference Proceedings (OSTI)

This project is the first large pilot scale test of a new process to passivate the carbon in ash so that it can be used in concrete without physically removing the carbon from the ash. The tests were conducted at PPL's Montour SES, sponsored by DOE and supported by EPRI. Near full-scale industrial equipment was used to expose fly ash, carbon mixtures to ozone to see if ozone would passivate the surface of carbon so that it would not react with air entraining agents that are used by concrete manufacturers...

2005-11-29T23:59:59.000Z

273

Ozone removal capability of a welding fume respirator containing activated charcoal  

SciTech Connect

Development of air purifying respirators for protection against ozone has been slowed by concerns about oxidation of charcoal and other available sorbents. The suitability of a charcoal sorbent for low concentrations of ozone was evaluated as a part of the development of a half-mask air purifying respirator designed for welding fumes and ozone. Testing of the respirator confirmed that charcoal can be a suitable sorbent for low levels of ozone. Where the respirator is properly selected, fit tested, and worn, respirator use against welding fumes and ozone at concentrations not exceeding 10 times the permissible exposure limit had been recommended.

Johnston, A.R.; Dyrud, J.F.; Shih, Y.T. (Occupational Health and Environmental Safety Division, St. Paul, MN (USA))

1989-09-01T23:59:59.000Z

274

Enhanced solubility of petroleum hydrocarbons using biosurfactants  

E-Print Network (OSTI)

This research investigation included two similarly-designed experiments. In the first, a biological surfactant produced by Rhodococcus strain H13-A and a commonly-used synthetic surfactant, Tween-80 (polyoxyethylene sorbitan monooleate), were compared for their effectiveness in enhancing the transport of polycyclic aromatic hydrocarbons from a complex organic phase into aqueous solution. In the batch-reactor experiment, each reactor contained a surfactant solution and West Texas Crude oil, while the control reactors contained distilled-deionized water and the crude oil. Using a temporal-monitoring scheme, the reactors were sacrificially sampled to determine the water-accommodated fraction (WAF). The phenanthrenes, fluorenes, pyrenes, and chrysenes showed significant increases in their aqueous-plus-micellar-phase concentrations in the presence of surfactants; the increase was greater for the biosurfactant compared to the synthetic surfactant. The enhancement in "solubility" was also more significant for the highly-substituted aromatics, when compared to their parent compounds. In the second study, the effects of four biosurfactants on the solubility of petroleum saturated hydrocarbons were compared. Rhodococcus species H13-A (glycolipid-producing), Pseudomonas aeruginosa ATCC 9027 (rhamnolipid-producing), Candida bombicola ATCC 22214 (sophorolipid-producing), and Bacillus subtilis ATCC 21332 (surfactin-producing) were compared to a control of distilled-deionized water. The experimental design was similar that of the first study. The Pseudomonas aeruginosa treatment significantly enhanced the solubility of the lower-weight, higher-weight and branched saturated hydrocarbons. The Rhodococcus treatment significantly enhanced the solubility of the low-molecular-weight compounds, but only moderately increased the solubilities of the other saturates. Neither the Candida nor the Bacillus solutions produced any negligible increase in solubility under these laboratory conditions.

Page, Cheryl Ann

1997-01-01T23:59:59.000Z

275

Collisional processes of hydrocarbons in hydrogen plasmas  

DOE Green Energy (OSTI)

We have investigated the reactions of methane and its derivatives with hydrogen plasmas for use in modelling carbon and hydrocarbon transport in hydrogen plasmas. We provide quantitative information over the temperature range from 0.1 eV to 2 keV for the most significant reactions of methane and methane fragments with electrons and protons. We review the properties of each reaction, present graphs of the cross section and reaction rate coefficient, and give analytical fits for sigma and (sigmav). 34 refs.

Ehrhardt, A.B.; Langer, W.D.

1987-09-01T23:59:59.000Z

276

Clean Cities ozone air quality attainment and maintenance strategies that employ alternative fuel vehicles, with special emphasis on natural gas and propane  

DOE Green Energy (OSTI)

Air quality administrators across the nation are coming under greater pressure to find new strategies for further reducing automotive generated non-methane hydrocarbon (NMHC) and nitrogen oxide (NOx) emissions. The US Environmental Protection Agency (EPA) has established stringent emission reduction requirements for ozone non-attainment areas that have driven the vehicle industry to engineer vehicles meeting dramatically tightened standards. This paper describes an interim method for including alternative-fueled vehicles (AFVs) in the mix of strategies to achieve local and regional improvements in ozone air quality. This method could be used until EPA can develop the Mobile series of emissions estimation models to include AFVs and until such time that detailed work on AFV emissions totals by air quality planners and emissions inventory builders is warranted. The paper first describes the challenges confronting almost every effort to include AFVs in targeted emissions reduction programs, but points out that within these challenges resides an opportunity. Next, it discusses some basic relationships in the formation of ambient ozone from precursor emissions. It then describes several of the salient provisions of EPA`s new voluntary emissions initiative, which is called the Voluntary Mobile Source Emissions Reduction Program (VMEP). Recent emissions test data comparing gaseous-fuel light-duty AFVs with their gasoline-fueled counterparts is examined to estimate percent emissions reductions achievable with CNG and LPG vehicles. Examples of calculated MOBILE5b emission rates that would be used for summer ozone season planning purposes by an individual Air Quality Control Region (AQCR) are provided. A method is suggested for employing these data to compute appropriate voluntary emission reduction credits where such (lighter) AFVs would be acquired. It also points out, but does not quantify, the substantial reduction credits potentially achievable by substituting gaseous-fueled for gasoline-fueled heavy-duty vehicles. Finally, it raises and expands on the relevance of AFVs and their deployment to some other provisions embedded in EPA`s current guidance for implementing 1-hour NAAQS--standards which currently remain in effect--as tools to provide immediate reductions in ozone, without waiting for promised future clean technologies.

Santini, D.J.; Saricks, C.L.

1998-08-04T23:59:59.000Z

277

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

SciTech Connect

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

278

Carbon monoxide in indoor ice skating rinks: Evaluation of absorption by adult hockey players  

Science Conference Proceedings (OSTI)

We evaluated alveolar carbon monoxide (CO) levels of 122 male, adult hockey players active in recreational leagues of the Quebec City region (Canada), before and after 10 weekly 90-minute games in 10 different rinks. We also determined exposure by quantifying the average CO level in the rink during the games. Other variables documented included age, pulmonary function, aerobic capacity, and smoking status. Environmental concentrations varied from 1.6 to 131.5 parts per million (ppm). We examined the absorption/exposure relationship using a simple linear regression model. In low CO exposure levels, physical exercise lowered the alveolar CO concentration. However, we noted that for each 10 ppm of CO in the ambient air, the players had adsorbed enough CO to raise their carboxyhemoglobin (COHb) levels by 1 percent. This relationship was true both for smokers and non-smokers. We suggest that an average environmental concentration of 20 ppm of CO for the duration of a hockey game (90 minutes) should be reference limit not to be exceeded in indoor skating rinks.

Levesque, B.; Dewailly, E.; Lavoie, R.; Prud'Homme, D.; Allaire, S. (Centre hospitalier de l'Universite Laval, Quebec City (Canada))

1990-05-01T23:59:59.000Z

279

Review Article A Review on Preferential Oxidation of Carbon Monoxide in Hydrogen Rich Gases  

E-Print Network (OSTI)

In this review, recent works on the preferential oxidation of carbon monoxide in hydrogen rich gases for fuel cell applications are summarized. H2 is used as a fuel for polymer-electrolyte membrane fuel cell (PEMFC). It is produced by reforming of natural gas or liquid fuels followed by water gas shift reaction. The produced gas consists of H2, CO, and CO2. In which CO content is around 1%, which is highly poisonous for the Pt anode of the PEMFC so that further removal of CO is needed. Catalytic preferential oxidation of CO (CO-PROX) is one of the most suitable methods of purification of H2 because of high CO conversion rate at low temperature range, which is preferable for PEMFC operating conditions. Catalysts used for CO-PROX are mainly noble metal based; gold based and base metal oxide catalysts among them Copper-Ceria based catalysts are the most appropriate due to its low cost, easy availability and result obtained by these catalysts are comparable with the conventional noble metal catalysts. Copyright © 2011 by BCREC UN-

A. Mishra; R. Prasad

2010-01-01T23:59:59.000Z

280

Highly ordered magnetic mesoporous silicas for effective elimination of carbon monoxide  

Science Conference Proceedings (OSTI)

Catalysts based on crystalline nanoparticles of Fe metal supported on mesoporous silica have been developed. The synthetic process involves hydrogen reduction processing for high abundant Fe metal nanoparticles within the mesopores, in which impregnated Fe salt in the inner nanopores of mesoporous silica is thermally treated under hydrogen at 500 Degree-Sign C. Detailed characterization was achieved by XRD, XPS, BET, and HR-TEM techniques. The catalytic efficiency was demonstrated as a function of the used amounts and reaction time. The results show that more than 90% of the carbon monoxide was eliminated at room temperature during a period 80 min with 0.5 g of catalyst. - Graphical abstract: Strategy for the preparation of highly abundant Fe nanoparticle embedded MS catalyst by hydrogen reduction process and HR-TEM images of cross-sectional and top view. Highlights: Black-Right-Pointing-Pointer MS based heterogeneous catalyst with Fe nanoparticles were demonstrated for CO elimination. Black-Right-Pointing-Pointer Highly Fe nanoparticle embedded MS catalyst prepared by hydrogen reduction process. Black-Right-Pointing-Pointer Systematic characterization was achieved by XRD, XPS, BET, and HR-TEM analyses. Black-Right-Pointing-Pointer More than 90% of the CO was eliminated at RT during 80 min with 0.5 g of catalyst.

Lee, Jiho [Korea Institute of Ceramic Engineering and Technology, Seoul 153-801 (Korea, Republic of); Department of Chemistry, Inha University, Incheon 402-751 (Korea, Republic of); Ho Chang, Jeong, E-mail: jhchang@kicet.re.kr [Korea Institute of Ceramic Engineering and Technology, Seoul 153-801 (Korea, Republic of)

2012-04-15T23:59:59.000Z

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.


281

Meteorology-induced variations in the spatial behavior of summer ozone pollution in Central California  

SciTech Connect

Cluster analysis was applied to daily 8 h ozone maxima modeled for a summer season to characterize meteorology-induced variations in the spatial distribution of ozone. Principal component analysis is employed to form a reduced dimension set to describe and interpret ozone spatial patterns. The first three principal components (PCs) capture {approx}85% of total variance, with PC1 describing a general spatial trend, and PC2 and PC3 each describing a spatial contrast. Six clusters were identified for California's San Joaquin Valley (SJV) with two low, three moderate, and one high-ozone cluster. The moderate ozone clusters are distinguished by elevated ozone levels in different parts of the valley: northern, western, and eastern, respectively. The SJV ozone clusters have stronger coupling with the San Francisco Bay area (SFB) than with the Sacramento Valley (SV). Variations in ozone spatial distributions induced by anthropogenic emission changes are small relative to the overall variations in ozone amomalies observed for the whole summer. Ozone regimes identified here are mostly determined by the direct and indirect meteorological effects. Existing measurement sites are sufficiently representative to capture ozone spatial patterns in the SFB and SV, but the western side of the SJV is under-sampled.

Jin, Ling; Harley, Robert A.; Brown, Nancy J.

2010-06-23T23:59:59.000Z

282

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

DOE Green Energy (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

283

Preliminary Geospatial Analysis of Arctic Ocean Hydrocarbon Resources  

SciTech Connect

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

284

Geology and hydrocarbon potentials of Arafura Sea  

Science Conference Proceedings (OSTI)

The Arafura Sea is a continental-shelf sea located between Irian Jaya (western New Guinea) and the northern part of the Australian continent. On the south it adjoins the stable Australian craton, and on the north it is bordered by the Tertiary collision zone between the Australian craton and the northern Irian Jaya island arc. On the west and northwest it is bounded by the active Banda arc collision zone, whereas on the east it is bordered by the northern extension of the Gulf of Carpentaria that also forms the western limit of the zone of late Paleozoic granites. Shelf sediments, ranging in age from late Paleozoic to Cenozoic, predominate in the Arafura Sea continental shelf, and are underlain by granitic basement. Gas shows have been reported from Jurassic to Cretaceous fine-grained marine limestones and sandstones, and gas and condensate also are present in Cretaceous sediments and Middle Jurassic fine-grained sandstones. At the north, the most prospective area seems to be the hinge zone of the Aru high, where a combination of traps and reservoir rocks presumably exists. On the south, the Money Shoal area is considered a significant prospect. In the Arafura basin, stratigraphic traps seem to be the most promising target for hydrocarbon exploration as tectonics seems not to have played an important role in the area. The sedimentary area occupied by the eastern extension of the Tarera-Aiduna wrench fault should also be investigated in detail for its hydrocarbon potential.

Katili, J.A.

1984-09-01T23:59:59.000Z

285

Lubricant formulation for lower unburnt hydrocarbon emissions  

Science Conference Proceedings (OSTI)

Engine-out emissions of unburnt hydrocabons from spark ignition engines are attributable to a number of mechanisms, occurring during the engine cycle, by which fuel escapes combustion. These include absorption of fuel components into the bore lubricating oil film during compression, and subsequent desorption into hot combustion gases throughout expansion. A proportion of the hydrocarbons desorbed will then be emitted, either as unburnt or partially oxidised fuel. This mechanism has been studied by a number of workers, and estimates of its importance vary from 10 to 30% of total hydrocarbons being related to the absorption/desorption process. A novel lubricant additive has been formulated for the purpose of reducing the quantity of fuel which is absorbed into the bore lubricant film, and hence the quantity of fuel subsequently desorbed. This paper describes a programme to evaluate the effect that this lubricant additive can have on engine-out emissions from a single cylinder research engine, together with results from current technology, low-emitting US and European vehicles, tested over FTP and ECE drive cycles. 11 refs., 9 figs., 3 tabs.

Beckwith, P.; Cooper, J.H.

1994-10-01T23:59:59.000Z

286

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

287

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

288

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

289

Algal Lipid Extraction and Upgrading to Hydrocarbons Technology Pathway  

DOE Green Energy (OSTI)

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, R.; Biddy, M.; Jones, S.

2013-03-01T23:59:59.000Z

290

Biological Conversion of Sugars to Hydrocarbons Technology Pathway  

DOE Green Energy (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

291

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

292

An Analysis of the Power Spectra of Total Ozone Data  

Science Conference Proceedings (OSTI)

An analysis is made of the power spectrum of total ozone data using the window closing procedure of Jenkins and Watts (1968). It is concluded that it is presently difficult to distinguish statistically between true periodicities in the data and a ...

Paul V. Rigterink

1981-04-01T23:59:59.000Z

293

Lake Michigan Membrane/Ozone Research and Demonstration Study  

Science Conference Proceedings (OSTI)

Drinking water standards in the United States have become increasingly stringent. The recently-promulgated Enhanced Surface Water Treatment Rule (ESWTR) requires controlling for Cryptosporidium, a pathogen that is resistant to chlorine. This report evaluates the effectiveness of membrane and ozone technologies for reducing Cryptosporidium risks.

1999-12-30T23:59:59.000Z

294

On the Relation between Atmospheric Ozone and Sunspot Number  

Science Conference Proceedings (OSTI)

Based on data from the Dobson network, between 1960 and 1987 there has been a zero-lag correlation of 0.48 between the 112 unsmoothed seasonal values of sunspot number and global total ozone, significant at the 1% level taking into account the ...

J. K. Angell

1989-11-01T23:59:59.000Z

295

Ozone Destruction in Continental Stratus Clouds: An Aircraft Case Study  

Science Conference Proceedings (OSTI)

Apparent depletion of ozone in a cold (0°C), continental stratus cloud system was observed during in situ data collection on 30 April 1994 at the Department of Energy Clouds and Radiation Test Bed site in northern Oklahoma. Analyses of the ...

Zhien Wang; Kenneth Sassen

2000-06-01T23:59:59.000Z

296

Photochemical Modeling of Two 1984 SCCCAMP Ozone Episodes  

Science Conference Proceedings (OSTI)

Data collected during the 1984 SCCCAMP Exploratory Study were used to develop two multiple-day ozone modeling episodes for the Urban Airshed Model (UAM). An operational model performance evaluation was performed for the 5–7 and 16–17 September ...

T. W. Tesche; Dennis E. McNally

1991-05-01T23:59:59.000Z

297

Ozone injury to tobacco plants in South Dakota  

SciTech Connect

Ozone injury symptoms appeared on tobacco (Nicotiana tabacum) Turkish in the greenhouse and on Wisconsin 38 in field plots at Brookings, South Dakota in 1970. In 1971, ozone injury appeared on greenhouse and field-grown plants of Bel-W3, Bel-C, and Turkish. Ozone fleck was most severe in southeast and east-central South Dakota. A decreasing amount of injury was observed in northeast, central, west-central and southwest South Dakota. Bel-W3 showed injury at eight locations while Turkish, Bel-C and Bel-B were injured only in the eastern parts of the State. Bel-W3 was a reliable monitor of air pollution episodes when plants were continuously produced and observed in the greenhouse at Brookings. New injury appeared on newly matured leaves and older leaves as dark gray to black flecks that turned brown to tan to white with age. Periodic ozone occurrences were recorded by new flecks appearing generally on tissue of younger age. Plant indicators for the pollutants peroxyacetyl-nitrate, fluoride and sulfur dioxide showed no injury in South Dakota. 21 references, 4 figures, 1 table.

Gardner, W.S.

1973-02-01T23:59:59.000Z

298

Geologic control of natural marine hydrocarbon seep emissions, Coal Oil Point seep field, California  

E-Print Network (OSTI)

Formation, the primary source of petroleum hydrocarbons inPetroleum Geologists, Tulsa Clark JF, Washburn L, Hornafius JS, Luyendyk BP (2000) Natural marine hydrocarbon seep source

Leifer, Ira; Kamerling, Marc J.; Luyendyk, Bruce P.; Wilson, Douglas S.

2010-01-01T23:59:59.000Z

299

The Spatial Scales, Distribution, and Intensity of Natural Marine Hydrocarbon Seeps near Coal Oil Point, California  

E-Print Network (OSTI)

marine hydrocarbon seeps (Coal Oil Point, Santa Barbara,marine hydrocarbon seepage near Coal Oil Point, California,associated with offshore oil production", Geology, 27(11),

Washburn, Libe; Clark, Jordan F.; Kyriakidis, Phaedon

2004-01-01T23:59:59.000Z

300

The Spatial Scales, Distribution, and Intensity of Natural Marine Hydrocarbon Seeps near Coal Oil Point, California  

E-Print Network (OSTI)

marine hydrocarbon seeps (Coal Oil Point, Santa Barbara,marine hydrocarbon seepage near Coal Oil Point, California,source areas such as near Coal Oil Point. Furthermore,

Washburn, Libe; Clark, Jordan F.; Kyriakidis, Phaedon

2004-01-01T23:59:59.000Z

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.


301

Cogeneration systems and processes for treating hydrocarbon containing formations  

Science Conference Proceedings (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

302

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

303

Ozone effects on inhibitors of human neutrophil proteinases  

SciTech Connect

The effects of ozone on human alpha 1-proteinase inhibitor (A-1-PI), alpha 1-antichymotrypsin (A-1-Achy), bronchial leukocyte proteinase inhibitor (BLPI), and Eglin C were studied using in vitro exposures in phosphate-buffered solutions. Following ozone exposure, inhibitory activities against human neutrophil elastase (HNE) and/or cathepsin G (Cat G) were measured. Exposure of A-1-PI to 50 mol O3/mol protein resulted in a complete loss of HNE inhibitory activity, whereas A-1-Achy lost only 50% of its Cat G inhibitory activity and remained half active even after exposure to 250 mol of O3. At 40 mol O3/mol protein, BLPI lost 79% of its activity against HNE and 87% of its Cat G inhibitory activity. Eglin C, a leech-derived inhibitor, lost 81% of its HNE inhibitory activity and 92% of its ability to inhibit Cat G when exposed to 40 mol O3/mol. Amino acid analyses of ozone-exposed inhibitors showed destruction of Trp, Met, Tyr, and His with as little as 10 mol O3/mol protein, and higher levels of O3 resulted in more extensive oxidation of susceptible residues. The variable ozone susceptibility of the different amino acid residues in the four proteins indicated that oxidation was a function of protein structure, as well as the inherent susceptibility of particular amino acids. Exposure of A-1-PI and BLPI in the presence of the antioxidants, Trolox C (water soluble vitamin E) and ascorbic acid (vitamin C), showed that antioxidant vitamins may protect proteins from oxidative inactivation by ozone. Methionine-specific modification of BLPI reduced its HNE and Cat G inhibitory activities. Two moles of N-chlorosuccinimide per mole of BLPI methionine caused an 80% reduction in activity against Cat G, but only a 40% reduction in HNE inhibitory activity.

Smith, C.E.; Stack, M.S.; Johnson, D.A.

1987-02-15T23:59:59.000Z

304

SOFT X-RAY IRRADIATION OF PURE CARBON MONOXIDE INTERSTELLAR ICE ANALOGUES  

SciTech Connect

There is an increasing evidence for the existence of large organic molecules in the interstellar and circumstellar medium. Very few among such species are readily formed in conventional gas-phase chemistry under typical conditions of interstellar clouds. Attention has therefore focused on interstellar ices as a potential source of these relatively complex species. Laboratory experiments show that irradiation of interstellar ice analogues by fast particles or ultraviolet radiation can induce significant chemical complexity. However, stars are sources of intense X-rays at almost every stage of their formation and evolution. Such radiation may thus provide chemical changes in regions where ultraviolet radiation is severely inhibited. After H{sub 2}O, CO is often the most abundant component of icy grain mantles in dense interstellar clouds and circumstellar disks. In this work we present irradiation of a pure carbon monoxide ice using a soft X-ray spectrum peaked at 0.3 keV. Analysis of irradiated samples shows formation of CO{sub 2}, C{sub 2}O, C{sub 3}O{sub 2}, C{sub 3}, C{sub 4}O, and CO{sub 3}/C{sub 5}. Comparison of X-rays and ultraviolet irradiation experiments, of the same energy dose, shows that X-rays are more efficient than ultraviolet radiation in producing new species. With the exception of CO{sub 2}, X-ray photolysis induces formation of a larger number of products with higher abundances, e.g., C{sub 3}O{sub 2} column density is about one order of magnitude higher in the X-ray experiment. To our knowledge this is the first report on X-ray photolysis of CO ices. The present results show that X-ray irradiation represents an efficient photo-chemical way to convert simple ices to more complex species.

Ciaravella, A.; Candia, R.; Collura, A. [INAF-Osservatorio Astronomico di Palermo, P.za Parlamento 1, 90134 Palermo (Italy); Jimenez-Escobar, A.; Munoz Caro, G. M. [Centro de Astrobiologia (CSIC-INTA), Carretera de Ajalvir, km 4, Torrejon de Ardoz, 28850 Madrid (Spain); Cecchi-Pestellini, C. [INAF-Osservatorio Astronomico di Cagliari, Strada n.54, Loc. Poggio dei Pini, I-09012 Capoterra (Italy); Giarrusso, S. [INAF-Istituto di Astrofisica Spaziale e Fisica Cosmica, Via U. La Malfa 153, I-90146 Palermo (Italy); Barbera, M., E-mail: aciaravella@astropa.unipa.it [Dipartimento di Scienze Fisiche and Astronomiche, Universita di Palermo, Sezione di Astronomia, Piazza del Parlamento 1, I-90134 Palermo (Italy)

2012-02-10T23:59:59.000Z

305

Reaction of uranium oxides with chlorine and carbon or carbon monoxide to prepare uranium chlorides  

SciTech Connect

The preferred preparation concept of uranium metal for feed to an AVLIS uranium enrichment process requires preparation of uranium tetrachloride (UCI{sub 4}) by reacting uranium oxides (UO{sub 2}/UO{sub 3}) and chlorine (Cl{sub 2}) in a molten chloride salt medium. UO{sub 2} is a very stable metal oxide; thus, the chemical conversion requires both a chlorinating agent and a reducing agent that gives an oxide product which is much more stable than the corresponding chloride. Experimental studies in a quartz reactor of 4-cm ID have demonstrated the practically of some chemical flow sheets. Experimentation has illustrated a sequence of results concerning the chemical flow sheets. Tests with a graphite block at 850{degrees}C demonstrated rapid reactions of Cl{sub 2} and evolution of carbon dioxide (CO{sub 2}) as a product. Use of carbon monoxide (CO) as the reducing agent also gave rapid reactions of Cl{sub 2} and formation of CO{sub 2} at lower temperatures, but the reduction reactions were slower than the chlorinations. Carbon powder in the molten salt melt gave higher rates of reduction and better steady state utilization of Cl{sub 2}. Addition of UO{sub 2} feed while chlorination was in progress greatly improved the operation by avoiding the plugging effects from high UO{sub 2} concentrations and the poor Cl{sub 2} utilizations from low UO{sub 2} concentrations. An UO{sub 3} feed gave undesirable effects while a feed of UO{sub 2}-C spheres was excellent. The UO{sub 2}-C spheres also gave good rates of reaction as a fixed bed without any molten chloride salt. Results with a larger reactor and a bottom condenser for volatilized uranium show collection of condensed uranium chlorides as a loose powder and chlorine utilizations of 95--98% at high feed rates. 14 refs., 7 figs., 14 tabs.

Haas, P.A.; Lee, D.D.; Mailen, J.C.

1991-11-01T23:59:59.000Z

306

Stable isotope investigations of chlorinated aliphatic hydrocarbons.  

Science Conference Proceedings (OSTI)

Stable isotope ratio measurements for carbon (C) and chlorine (Cl) can be used to elucidate the processes affecting transformation and transportation of chlorinated aliphatic hydrocarbons (CAHs) in the environment. Methods recently developed in our laboratory for isotopic analysis of CAHs have been applied to laboratory measurements of the kinetic isotope effects associated with aerobic degradation of dichloromethane (DCM) and with both anaerobic and aerobic cometabolic degradation of trichlomethene (TCE) in batch and column microbial cultures. These experimental determinations of fractionation factors are crucial for understanding the behavior of CAHs in complex natural systems, where the extent of biotransformation can be masked by dispersion and volatilization. We have also performed laboratory investigations of kinetic isotope effects accompanying evaporation of CAHs, as well as field investigations of natural attenuation and in situ remediation of CAHs in a number of contaminated shallow aquifers at sites operated by the federal government and the private sector.

Abrajano, T.; Heraty, L. J.; Holt, B. D.; Huang, L.; Sturchio, N. C.

1999-06-01T23:59:59.000Z

307

Microbial hydrocarbons: back to the future  

Science Conference Proceedings (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

308

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

309

Observed and WRF-Simulated Low-Level Winds in a High-Ozone Episode during the Central California Ozone Study  

Science Conference Proceedings (OSTI)

A case study is carried out for the 29 July–3 August 2000 episode of the Central California Ozone Study (CCOS), a typical summertime high-ozone event in the Central Valley of California. The focus of the study is on the low-level winds that ...

J-W. Bao; S. A. Michelson; P. O. G. Persson; I. V. Djalalova; J. M. Wilczak

2008-09-01T23:59:59.000Z

310

Preignition oxidation characteristics of hydrocarbon fuels  

SciTech Connect

Experimental results obtained from a static reactor are presented for the oxidation of a variety of fuels. Pressure and temperature histories of the reacting fuel/oxidizer mixtures were obtained. Measurements of the stable reaction intermediate and product species were made using gas chromatographic analysis. One aspect of this work involved detailed studies of the oxidation chemistry of relatively low molecular weight aliphatic hydrocarbons: propane, propene, and n-butane. The oxidation chemistry of these fuels was examined at temperatures in the range 550-750 K, equivalence ratios ranging from 0.8 to 4.0 and at subatmospheric pressures. The main characteristics and features of the oxidation mechanisms were determined for each fuel in each temperature regime. The experimental results from propene and propane were used to develop a low and intermediate temperature kinetic mechanism for these fuels based on a low temperature acetaldehyde mechanism of Kaiser et al. and a high temperature propene/propane mechanism of Westbrook and Pitz. General preignition characteristics of higher molecular weight hydrocarbons and binary mixtures of these fuels were also studied. The low temperature/cool flame ignition characteristics of dodecane were investigated at temperatures in the range 523-623 K, equivalence s ranging from 0.8 to 1.0 and at subatmospheric pressures. The preignition characteristics of binary mixtures of dodecane and the aromatic component tetralin were examined. The addition of the tetralin had the overall effect of decreasing the ignition tendency of the mixture, although this effect was nonlinear with respect to the amount of tetralin added.

Wilk, R.D.

1986-01-01T23:59:59.000Z

311

Solubilization of petroleum hydrocarbons using biosurfactants  

E-Print Network (OSTI)

Low solubility of petroleum hydrocarbons in water is the major factor limiting the degradation rates of these compounds (Zhang and Miller, 1994). The fraction that is more soluble in the aqueous phase is degraded at higher rates, while less soluble or insoluble compounds have lower degradation rates due to limited bioavailability to the microbial community. A recent study in our lab found no significant degradation of weathered petroleum at a Texas petrochemical plant site. It was concluded 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., 1994). This research focused on biosurfactants because they have been shown to be as effective as chemical surfactants and, most importantly, they enhance biodegradation. Glycolipid biosurfactants are produced by Rhodococcus species HI 3-A to enhance substrate solubility and promote bioavailability for degradation. The work proceeded in two stages. The initial stage involved production and characterization of extracellular biosurfactants by HI 3-A when grown on minimal salts media with hexadecane as the carbon source. The second stage evaluated the performance of the biosurfactants in enhancing the aqueous solubility of weathered West Texas Crude. Initial results indicated production of the biosurfactants by Rhodococcus species H13-A during the stationary growth stage. Biosurfactants lowered the surface tension from 72 to-30 dynes/cm and interfacial tension to below 5 dynes/cm. The two-, three-, and four-ring aromatic compounds showed substantial increase in their aqueous phase concentrations in the presence of biosurfactants. The enhancement was more dramatic with the larger aromatics and also the highly substituted-compounds. Preliminary experiments on toxicity and biodegradation indicated higher levels of toxicity in the surfactant/aqueous mixtures due to increased PAH partitioning (Lambert, 1995), and increased degradation rates for the target PAH compounds.

Kanga, Shahrukh

1995-01-01T23:59:59.000Z

312

Ozone (o3) efficacy on reduction of phytophthora capsici in recirculated horticultural irrigation water  

E-Print Network (OSTI)

Microorganisms that cause plant disease have been isolated in recirculated irrigation water and increase the risks of disease incidence in horticultural operations. Ozone is an effective oxidizer used to disinfect drinking water supplies and treat industrial wastewater. The objective of this research was to investigate using ozone gas as part of a strategy to reduce the incidence of Phytophthora deBary in recirculated irrigation water. An isolate of Phytophthora capsici Leonian was cultured to induce sporulation. Spore dilutions were placed in aliquots of reverse osmosis water and bubbled with ozone gas (O3) to concentrations of 0 to 1.5 mg·L-1. Ozonated samples were plated and observed for colony forming units. Increasing ozone concentrations reduced the number of colony forming units to 0 at 1.5 mg· L-1 03. Turbidity effects on efficacy on Phytophthora capsici were tested using bentonite clay at 0 to 2.0 nephelometric turbidity units and ozone concentrations of 0 to 1.5 mg· L-1. Increasing bentonite did not affect the efficacy of increasing ozone concentrations on reducing colony formation to 0 at 1.5 mg·L-1 O3. Bioassays using Phytophthora capsici on Capsicum annuum L. seedlings confirmed apparent pathogenicity. Reverse osmosis water, containing a soluble fertilizer at 0 to 300 mg· L-1 N, was ozonated to concentrations of 0 to 1.5 mg·L-1 O3 and used to irrigate Chrysanthemum x morifolium T. de Romatuelle. Increasing ozone concentrations did not interact with increasing fertilizer levels to affect the final growth parameters. Chrysanthemum exposed to ozone gas concentrations of 0.5 to 1.5 mg·L-1 showed symptomatic ozone damage. Complete soluble fertilizer solutions with micronutrients were ozonated from 0 to 1.5 mg·L-1 O3 and analysed for nutrient content. Increasing ozone levels did not interact with fertilizers to affect macronutrients. Increasing ozone interacted with iron at a high fertilizer level. Ozone did not affect the efficacy of paclobutralzol in controlling growth in Viola x wittrockiana. Ozone was effective in controlling Phytophthora capsici in recirculated irrigation water with minimum impact on plant growth. Adjustments in fertility regiemes may be needed to counteract the oxidizing affect of ozone on micronutrients.

McDonald, Garry Vernon

2007-05-01T23:59:59.000Z

313

Thermodynamic investigation into steam-methane reforming and the synthesis of methane from carbon monoxide and hydrogen  

SciTech Connect

In this study the stream-methane equilibrium reaction was investigated by considering both methane synthesis from hydrogen and carbon monoxide and by considering steam-methane reforming from methane and steam. A FORTRAN computer program was written to carry out all the calculations over a wide range of temperatures, pressures, and initial compositions. The products of each process as a function of pressure, temperature, and starting ratio of reactant gases were calculated, as well as the heats involved. In both processes the minimum ratios above which no carbon precipitates were determined as a function of temperature and pressure were given.

Wu, L.H.; Lietzke, M.H.

1976-11-01T23:59:59.000Z

314

A two-dimensional model study of past trends in global ozone  

Science Conference Proceedings (OSTI)

Emissions and atmospheric concentrations of several trace gases important to atmospheric chemistry are known to have increased substantially over recent decades. Solar flux variations and the atmospheric nuclear test series are also likely to have affected stratospheric ozone. In this study, the LLNL two-dimensional chemical-radiative-transport model of the troposphere and stratosphere has been applied to an analysis of the effects that these natural and anthropogenic influences may have had on global ozone concentrations over the last three decades. In general, model determined species distributions and the derived ozone trends agree well with published analyses of land-based and satellite-based observations. Also, the total ozone and ozone distribution trends derived from CFC and other trace gas effects have a different response with latitude than the derived trends from solar flux variations, thus providing a ''signature'' for anthropogenic effects on ozone. 24 refs., 5 figs.

Wuebbles, D.J.; Kinnison, D.E.

1988-08-01T23:59:59.000Z

315

Thermal conversion of oil shale into recoverable hydrocarbons  

SciTech Connect

The production of hydrocarbons is accomplished by pyrolysis of oil shale with controlled removal of the resulting layer of spent oil-shale residue. A procedure is described for the in situ thermal conversion of oil shale wherein fluidized abrasive particles are employed to foster improved hydrocarbon production, in amount and kind, by a controlled partial removal of the layer of spent oil shale which results from application of flowing fluids to heat exposed surfaces of the oil shale to release hydrocarbons. (5 claims)

Slusser, M.L.; Bramhall, W.E.

1969-09-23T23:59:59.000Z

316

A pilot study of energy efficient air cleaning for ozone  

SciTech Connect

A laboratory pilot study has been undertaken with the material that showed the most promise (high capacity and low pressure drop) based on the literature review and associated calculations. The best-performing air cleaner was a commercially available pleated filter that contained a thin layer of small activated carbon particles between two sheets of non-woven fibrous webbing. We will refer to this unit as the ''ozone filter'' although it is marketed for removal of volatile organic compounds (VOCs) from automobile passenger compartments. This pilot study strongly suggests that ozone air cleaning can be practical in commercial air handling systems; however, further tests are needed to assess air cleaner performance under a wider range of conditions.

Gundel, Lara A.; Sullivan, Douglas P.; Katsapov, Gregory Y.; Fisk, William J.

2002-11-01T23:59:59.000Z

317

Scale-Up and Demonstration of Fly Ash Ozonation Technology  

Science Conference Proceedings (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

318

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

SciTech Connect

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

319

Ozone Alternative Disinfection Study for a Large-Scale Wastewater Treatment Plant  

Science Conference Proceedings (OSTI)

This report describes a feasibility study for the use of an ozonation disinfection system for the treatment of wastewater in the Passaic Valley.

1999-12-06T23:59:59.000Z

320

The Cost of Crop Damage Caused by Ozone Air Pollution From Motor Vehicles  

E-Print Network (OSTI)

D. T. Tingey, Assessment of Crop Loss From Air Pollutants,,Assessing Impacts of Ozone on Agricultural Crops: II.Crop Yield Functions and Alternative Exposure Statistics",

Delucchi, Mark A.; Murphy, James; Kim, Jin; McCubbin, Donald R.

1996-01-01T23:59:59.000Z

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

Secondary organic aerosol from ozone-initiated reactions with terpene-rich household products  

E-Print Network (OSTI)

analysis of competition between aerosol particle removal andof secondary organic aerosol. Part I: ?-pinene/ozone system.data when measuring ambient aerosol. Aerosol Science and

Coleman, Beverly K.

2008-01-01T23:59:59.000Z

322

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

323

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

324

The hydroxyl radical initiated oxidation of unsaturated hydrocarbons in the troposphere: a theoretical and experimental approach  

E-Print Network (OSTI)

Isoprene is the dominant non-methane organic compound emitted by vegetation into the atmosphere, with a global emission rate of ~ 500 Tg yr-1. Its oxidation serves as a major source of ground level ozone in North America during the summer months. Despite the significant impact on tropospheric chemistry, questions remain concerning the detailed oxidation mechanism. The initial step in the mechanism is the addition of OH to form four distinct isomers. The relative branching between these isomers influences the distribution of the final products. I present a comprehensive investigation into the mechanistic details of early steps in the oxidation mechanism of unsaturated hydrocarbons in the troposphere and employ theoretical and experimental techniques. To understand the detailed kinetics of the initial OH addition to unsaturated hydrocarbons, I first present a model developed for the ethylene-OH system. I present the details of a robust two-transition state model. I extend the developed two-transition state model to the case of OH addition to isoprene. Excellent agreement with observed temperature and pressure dependent rate constants affords a high confidence level in understanding of the kinetics and in the calculated branching ratio of the initial OH addition step. I then focus attention on the subsequent reactivity of the OH-isoprene adducts. Until recently, all four of the OH-isoprene adducts were supposed to have reacted with O2 via addition to form alkylperoxy radicals. Previous computational results suggest that two of the OH-isoprene adducts undergo an intramolecular cyclic isomerization followed by hydrogen abstraction by O2 to form stable carbonyl compounds. I have synthesized photolytic precursors, presenting a novel approach to probe the subsequent reactivity of individual hydroxyalkyl radicals. Initial verification of the cyclic isomerization pathway involved synthesis of the photolytic precursor corresponding to the 1,3-butadiene-OH adduct. A culmination of theoretical and experimental techniques allowed verification of the cyclic isomerization pathway. I synthesized the photolytic precursor, which provided a single isoprene-OH adduct. Employing laser photolysis/laser induced fluorescence, time-dependent multiplexed mass spectrometry, velocity map ion imaging, and theoretical techniques, we present the full characterization of the reactivity of the single isoprene-OH adduct in the presence of O2.

Tullos, Erin Elizabeth

2007-05-01T23:59:59.000Z

325

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

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

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

326

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

327

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

328

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

SciTech Connect

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

329

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

330

Trend Analysis for Atmospheric Hydrocarbon Partitioning Using Continuous Thermodynamics  

Science Conference Proceedings (OSTI)

The partitioning of atmospheric hydrocarbons into vapor and condensed phases when the species count is large is considered using the formalism of continuous thermodynamics. The vapor saturation pressures and condensate species distribution are ...

K. Harstad

2005-08-01T23:59:59.000Z

331

Biodegradation and phytoremediation of polycyclic aromatic hydrocarbons using mushroom compost.  

E-Print Network (OSTI)

??Soils contaminated with Polycyclic Aromatic Hydrocarbons (PAHs) are commonly found in petroleum, gas-work and wood-impregnation sites. Interest in the biodegradation and environmental fate of PAHs… (more)

Kodjo-Wayo, Lina Korkor

2006-01-01T23:59:59.000Z

332

Assessment of plant-derived hydrocarbons. Final report  

DOE Green Energy (OSTI)

A number of hydrocarbon producing plants are evaluated as possible sources of rubber, liquid fuels, and industrial lubricants. The plants considered are Euphorbia lathyris or gopher plant, milkweeds, guayule, rabbit brush, jojoba, and meadow foam. (ACR)

McFadden, K.; Nelson, S.H.

1981-09-30T23:59:59.000Z

333

Computer program for determining the thermodynamic properties of light hydrocarbons  

DOE Green Energy (OSTI)

This program was written to be used as a subroutine. The program determines the thermodynamics of light hydrocarbons. The following light hydrocarbons can be analyzed: butane, ethane, ethylene, heptane, hexane, isobutane, isopentane, methane, octane, pentane, propane and propylene. The subroutine can evaluate a thermodynamic state for the light hydrocarbons given any of the following pairs of state quantities: pressure and quality, pressure and enthalpy, pressure and entropy, temperature and pressure, temperature and quality and temperature and specific volume. These six pairs of knowns allow the user to analyze any thermodynamic cycle utilizing a light hydrocarbon as the working fluid. The Starling--Benedict--Webb--Rubin equation of state was used. A brief description, flowchart, listing and required equations for each subroutine are included.

Riemer, D.H.; Jacobs, H.R.; Boehm, R.F.; Cook, D.S.

1976-01-01T23:59:59.000Z

334

Computer program for determining the thermodynamic properties of light hydrocarbons  

DOE Green Energy (OSTI)

This program was written to be used as a subroutine. The program determines the thermodynamics of light hydrocarbons. The following light hydrocarbons can be analyzed: butane, ethane, ethylene, heptane, hexane, isobutane, isopentane, methane, octane, pentane, propane and propylene. The subroutine can evaluate a thermodynamic state for the light hydrocarbons given any of the following pairs of state quantities: pressure and quality, pressure and enthalpy, pressure and entropy, temperature and pressure, temperature and quality and temperature and specific volume. These six pairs of knowns allow the user to analyze any thermodynamic cycle utilizing a light hydrocarbon as the working fluid. The Starling-Benedict-Webb-Rubin equation of state was used. This report contains a brief description, flowchart, listing and required equations for each subroutine.

Riemer, D.H.; Jacobs, H.R.; Boehm, R.F.; Cook, D.S.

1976-07-01T23:59:59.000Z

335

Conversion of Pentose-Derived Furans into Hydrocarbon Fuels  

Science Conference Proceedings (OSTI)

We are interested in the conversion of biomass-derived hemicellulose into hydrocarbon molecules that can be used in the formulation of 'drop-in' fuels such as gasoline (C5-12), diesel (C10-20) and jet fuel (C9-16). Our focus lies on the use of furfuryl alcohol as a starting material since that is already produced commercially from hemicellulose-derived pentoses. The steps required to convert the latter into hydrocarbons are 1) oligomerization of furfuryl alcohol to form dimers (C10) and trimers (C15), and 2) hydrotreatment of the dimers and trimers to produce a mixture of linear hydrocarbons with carbon chain lengths in the range of diesel and jet fuels. However, furfuryl alcohol readily polymerizes to form resins in the presence of an acid catalyst, and the exothermic oligomerization must be carried out under reaction control. This presentation will discuss our progress in the development of this sugar-to-hydrocarbon pathway.

Moens, L.; Johnson, D. K.

2012-01-01T23:59:59.000Z

336

Internal energy and parameters of the order-disorder phase transition in titanium monoxide TiO{sub y}  

Science Conference Proceedings (OSTI)

Quantum-mechanical ab initio calculations are used to simulate the free energy functions for titanium monoxide TiO{sub y}. The effect of the long-range order of the Ti{sub 5}O{sub 5} type superstructure on the internal energy of the compound is studied by the supercell method. The dependences of the configuration entropy and free energy on the long-range order parameter are determined. It is found that the order-disorder phase transition in titanium monoxide must occur in accordance with the mechanism of the first-order phase transition with a critical value of the long-range order parameter of 0.971. The calculated parameters of the phase transition are compared with the experimental data and the results obtained using the model of point charges and by calculating the Madelung energy. It is concluded that the short-range order and the phonon entropy must be taken into account in calculating the equilibrium phase diagrams for strongly nonstoichiometric compounds.

Kostenko, M. G.; Rempel, A. A., E-mail: rempel@ihim.uran.ru [Russian Academy of Sciences, Institute of Solid-State Chemistry, Ural Branch (Russian Federation); Lukoyanov, A. V. [Ural Federal University (Russian Federation)

2013-06-15T23:59:59.000Z

337

One-dimensional turbulence model simulations of autoignition of hydrogen/carbon monoxide fuel mixtures in a turbulent jet  

Science Conference Proceedings (OSTI)

The autoignition of hydrogen/carbon monoxide in a turbulent jet with preheated co-flow air is studied using the one-dimensional turbulence (ODT) model. The simulations are performed at atmospheric pressure based on varying the jet Reynolds number and the oxidizer preheat temperature for two compositions corresponding to varying the ratios of H{sub 2} and CO in the fuel stream. Moreover, simulations for homogeneous autoignition are implemented for similar mixture conditions for comparison with the turbulent jet results. The results identify the key effects of differential diffusion and turbulence on the onset and eventual progress of autoignition in the turbulent jets. The differential diffusion of hydrogen fuels results in a reduction of the ignition delay relative to similar conditions of homogeneous autoignition. Turbulence may play an important role in delaying ignition at high-turbulence conditions, a process countered by the differential diffusion of hydrogen relative to carbon monoxide; however, when ignition is established, turbulence enhances the overall rates of combustion of the non-premixed flame downstream of the ignition point. (author)

Gupta, Kamlesh G.; Echekki, Tarek [Department of Mechanical and Aerospace Engineering, North Carolina State University, NC (United States)

2011-02-15T23:59:59.000Z

338

Catalytic Upgrading of Sugars to Hydrocarbons Technology Pathway  

DOE Green Energy (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

339

Hydrocarbon-enhanced particulate filter regeneration via microwave ignition  

DOE Patents (OSTI)

A regeneration method for a particulate filter includes estimating a quantity of particulate matter trapped within the particulate filter, comparing the quantity of particulate matter to a predetermined quantity, heating at least a portion of the particulate filter to a combustion temperature of the particulate matter, and introducing hydrocarbon fuel to the particulate filter. The hydrocarbon fuel facilitates combustion of the particulate matter to regenerate the particulate filter.

Gonze, Eugene V. (Pinckney, MI); Brown, David B. (Brighton, MI)

2010-02-02T23:59:59.000Z

340

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

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

Method for producing hydrocarbon fuels from heavy polynuclear hydrocarbons by use of molten metal halide catalyst  

DOE Patents (OSTI)

In a process for hydrocracking heavy polynuclear carbonaceous feedstocks to produce lighter hydrocarbon fuels by contacting the heavy feedstocks with hydrogen in the presence of a molten metal halide catalyst, thereafter separating at least a substantial portion of the carbonaceous material associated with the reaction mixture from the spent molten metal halide and thereafter regenerating the metal halide catalyst, an improvement comprising contacting the spent molten metal halide catalyst after removal of a major portion of the carbonaceous material therefrom with an additional quantity of hydrogen is disclosed.

Gorin, Everett (San Rafael, CA)

1979-01-01T23:59:59.000Z

342

Catalytic partial oxidation reforming of hydrocarbon fuels.  

DOE Green Energy (OSTI)

The polymer electrolyte fuel cell (PEFC) is the primary candidate as the power source for light-duty transportation systems. On-board conversion of fuels (reforming) to supply the required hydrogen has the potential to provide the driving range that is typical of today's automobiles. Petroleum-derived fuels, gasoline or some distillate similar to it, are attractive because of their existing production, distribution, and retailing infrastructure. The fuel may be either petroleum-derived or other alternative fuels such as methanol, ethanol, natural gas, etc. [1]. The ability to use a variety of fuels is also attractive for stationary distributed power generation [2], such as in buildings, or for portable power in remote locations. Argonne National Laboratory has developed a catalytic reactor based on partial oxidation reforming that is suitable for use in light-duty vehicles powered by fuel cells. The reactor has shown the ability to convert a wide variety of fuels to a hydrogen-rich gas at less than 800 C, temperatures that are several hundreds of degrees lower than alternative noncatalytic processes. The fuel may be methanol, ethanol, natural gas, or petroleum-derived fuels that are blends of various hydrocarbons such as paraffins, olefins, aromatics, etc., as in gasoline. This paper will discuss the results obtained from a bench-scale (3-kWe) reactor., where the reforming of gasoline and natural gas generated a product gas that contained 38% and 42% hydrogen on a dry basis at the reformer exit, respectively.

Ahmed, S.

1998-09-21T23:59:59.000Z

343

A Large Annual Cycle in Ozone above the Tropical Tropopause Linked to the Brewer–Dobson Circulation  

Science Conference Proceedings (OSTI)

Near-equatorial ozone observations from balloon and satellite measurements reveal a large annual cycle in ozone above the tropical tropopause. The relative amplitude of the annual cycle is large in a narrow vertical layer between 16 and 19 km, ...

William J. Randel; Mijeong Park; Fei Wu; Nathaniel Livesey

2007-12-01T23:59:59.000Z

344

Ozone Profile Retrieval from an Advanced Infrared Sounder: Experiments with Tropopause-Based Climatology and Optimal Estimation Approach  

Science Conference Proceedings (OSTI)

Motivated by a significant potential for retrieving atmospheric ozone profile information from advanced satellite infrared sounders, this study investigates various methods to optimize ozone retrievals. A set of retrieval experiments has been ...

Jennifer C. Wei; Laura L. Pan; Eric Maddy; Jasna V. Pittman; Murty Divarkarla; Xiaozhen Xiong; Chris Barnet

2010-07-01T23:59:59.000Z

345

Terannual Wave in the Ozone and Temperature in the Strato–Mesosphere as Deduced from Satellite Measurements  

Science Conference Proceedings (OSTI)

Two recent reference atmosphere models for ozone and temperature, which are deduced from satellite data, are employed to detect the existence and the behavior of a terannual wave both in ozone and temperature.

C. Varotsos; N. Dris; D. Asimakopoulos

1992-02-01T23:59:59.000Z

346

CCQM Activities in the Gas Analysis Working Group  

Science Conference Proceedings (OSTI)

... past two years included measurement of ammonia, hexane, propane, mercaptans, ozone, oxygen, carbon monoxide, carbon dioxide, nitric oxide ...

2012-11-16T23:59:59.000Z

347

Ozone-surface interactions: Investigations of mechanisms, kinetics, mass transport, and implications for indoor air quality  

SciTech Connect

In this dissertation, results are presented of laboratory investigations and mathematical modeling efforts designed to better understand the interactions of ozone with surfaces. In the laboratory, carpet and duct materials were exposed to ozone and measured ozone uptake kinetics and the ozone induced emissions of volatile organic compounds. To understand the results of the experiments, mathematical methods were developed to describe dynamic indoor aldehyde concentrations, mass transport of reactive species to smooth surfaces, the equivalent reaction probability of whole carpet due to the surface reactivity of fibers and carpet backing, and ozone aging of surfaces. Carpets, separated carpet fibers, and separated carpet backing all tended to release aldehydes when exposed to ozone. Secondary emissions were mostly n-nonanal and several other smaller aldehydes. The pattern of emissions suggested that vegetable oils may be precursors for these oxidized emissions. Several possible precursors and experiments in which linseed and tung oils were tested for their secondary emission potential were discussed. Dynamic emission rates of 2-nonenal from a residential carpet may indicate that intermediate species in the oxidation of conjugated olefins can significantly delay aldehyde emissions and act as reservoir for these compounds. The ozone induced emission rate of 2-nonenal, a very odorous compound, can result in odorous indoor concentrations for several years. Surface ozone reactivity is a key parameter in determining the flux of ozone to a surface, is parameterized by the reaction probability, which is simply the probability that an ozone molecule will be irreversibly consumed when it strikes a surface. In laboratory studies of two residential and two commercial carpets, the ozone reaction probability for carpet fibers, carpet backing and the equivalent reaction probability for whole carpet were determined. Typically reaction probability values for these materials were 10{sup {minus}7}, 10{sup {minus}5}, and 10{sup {minus}5} respectively. To understand how internal surface area influences the equivalent reaction probability of whole carpet, a model of ozone diffusion into and reaction with internal carpet components was developed. This was then used to predict apparent reaction probabilities for carpet. He combines this with a modified model of turbulent mass transfer developed by Liu, et al. to predict deposition rates and indoor ozone concentrations. The model predicts that carpet should have an equivalent reaction probability of about 10{sup {minus}5}, matching laboratory measurements of the reaction probability. For both carpet and duct materials, surfaces become progressively quenched (aging), losing the ability to react or otherwise take up ozone. He evaluated the functional form of aging and find that the reaction probability follows a power function with respect to the cumulative uptake of ozone. To understand ozone aging of surfaces, he developed several mathematical descriptions of aging based on two different mechanisms. The observed functional form of aging is mimicked by a model which describes ozone diffusion with internal reaction in a solid. He shows that the fleecy nature of carpet materials in combination with the model of ozone diffusion below a fiber surface and internal reaction may explain the functional form and the magnitude of power function parameters observed due to ozone interactions with carpet. The ozone induced aldehyde emissions, measured from duct materials, were combined with an indoor air quality model to show that concentrations of aldehydes indoors may approach odorous levels. He shows that ducts are unlikely to be a significant sink for ozone due to the low reaction probability in combination with the short residence time of air in ducts.

Morrison, Glenn C.

1999-12-01T23:59:59.000Z

348

JOURNAL OF GEOPHYSICAL RESEARCH, VOL. ???, XXXX, DOI:10.1029/, Ozone Ensemble Forecast with Machine Learning Algorithms  

E-Print Network (OSTI)

JOURNAL OF GEOPHYSICAL RESEARCH, VOL. ???, XXXX, DOI:10.1029/, Ozone Ensemble Forecast with Machine learning algorithms to perform sequential aggregation of ozone forecasts. The latter rely on a multimodel ensemble built for ozone forecasting with the modeling system Polyphemus. The ensemble simulations

Paris-Sud XI, Université de

349

Ozone levels in passenger cabins of commercial aircraft on North American  

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

Ozone levels in passenger cabins of commercial aircraft on North American Ozone levels in passenger cabins of commercial aircraft on North American and transoceanic routes Title Ozone levels in passenger cabins of commercial aircraft on North American and transoceanic routes Publication Type Journal Article Year of Publication 2008 Authors Bhangar, Seema, Shannon Cowlin, Brett C. Singer, Richard G. Sextro, and William W. Nazaroff Journal Environmental Science and Technology Volume 42 Issue 11 Pagination 3938-43 Abstract Ozone levels in airplane cabins, and factors that influence them, were studied on northern hemisphere commercial passenger flights on domestic U.S., transatlantic, and transpacific routes. Real-time data from 76 flights were collected in 2006-2007 with a battery-powered UV photometric monitor. Sample mean ozone level, peak-hour ozone level, and flight-integrated ozone exposures were highly variable across domestic segments (N = 68), with ranges of 100 ppbv) ozone levels on domestic flights were associated with winter-spring storms that are linked to enhanced exchange between the lower stratosphere and the upper troposphere.

350

Characterization of Ambient Ozone Levels in the Great Smoky Mountains National Park  

Science Conference Proceedings (OSTI)

Ambient ozone data collected at two sites in the Great Smoky Mountains National Park (GSMNP) are summarized and compared with data from an urban and a low-elevation rural site. The ozone climatology in the park is found to be similar to that of ...

Stephen F. Mueller

1994-04-01T23:59:59.000Z

351

An Improved Quality Control for AIRS Total Column Ozone Observations within and around Hurricanes  

Science Conference Proceedings (OSTI)

Atmospheric Infrared Sounder (AIRS) provides twice-daily global observations from which total column ozone data can be retrieved. However, 20% ~ 30% of AIRS ozone data are flagged to be of bad quality. Most of the flagged data were identified to ...

H. Wang; X. Zou; G. Li

2012-03-01T23:59:59.000Z

352

Effects of the Water Quality Maintained by Ozonation Enhanced Ecosystem in the Landscape of Reclaimed Water  

Science Conference Proceedings (OSTI)

the landscape of reclaimed water always broke out water bloom because of containing high concentrations of nitrogen and phosphorus. The TP and TN of the landscape decreased to 0.04mg/L and 2.27mg/L respectively with recycling ozonation at the end of ... Keywords: ozonation, algae, nutrient removal, ecosystem, landscape of reclaimed water

Yu Demiao; Ma Jun; Bai Yu; Gan Yiping

2009-10-01T23:59:59.000Z

353

New Ozone Measurement Systems for Autonomous Operation on Ocean Buoys and Towers  

Science Conference Proceedings (OSTI)

Two autonomous ozone measurement systems for use on ocean buoys and towers have been built and are discussed herein. They are based on low-power atmospheric ozone sensors from Physical Sciences Inc. (PSI) and 2B Technologies. The PSI sensor ...

E. J. Hintsa; G. P. Allsup; C. F. Eck; D. S. Hosom; M. J. Purcell; A. A. Roberts; D. R. Scott; E. R. Sholkovitz; W. T. Rawlins; P. A. Mulhall; K. Lightner; W. W. McMillan; J. Song; M. J. Newchurch

2004-07-01T23:59:59.000Z

354

Seasonal Differences in the Trend of Total Ozone and Contributions from Tropospheric and Stratospheric Layers  

Science Conference Proceedings (OSTI)

Based on an average of the total-ozone changes determined by means of linear regression at individual Dobson stations within climatic zones, trends of total ozone for each of the four seasons have been evaluated for five climatic zones, and the ...

J. K. Angell

1987-04-01T23:59:59.000Z

355

Estimating long term urban exposure to particulate matter and ozone in Europe  

Science Conference Proceedings (OSTI)

OFIS is a robust and efficient model for simulating the formation of photochemical pollutants in an urban plume. In this paper we present applications of the recent further development of OFIS for calculating both particulate matter and ozone concentrations. ... Keywords: Air quality model, Ozone exposure, PM exposure, Urban air pollution

Athanasios Arvanitis; Nicolas Moussiopoulos

2006-04-01T23:59:59.000Z

356

Ozone Forecasts of the Stratospheric Polar Vortex–Splitting Event in September 2002  

Science Conference Proceedings (OSTI)

The Southern Hemisphere major warming event in September 2002 has led to a breakup of the vortex in the middle and higher stratosphere and to a corresponding splitting of the ozone hole. Daily 3D ozone forecasts, produced at the Royal Netherlands ...

Henk Eskes; Arjo Segers; Peter van Velthoven

2005-03-01T23:59:59.000Z

357

The Ozone Weekend Effect in California: Evidence Supporting NOx Emission Reductions  

E-Print Network (OSTI)

Ozone is typically higher on weekends (WE) than on weekdays (WD) at many of California’s air-monitoring stations. Sometimes called the “ozone WE effect, ” this phenomenon occurs despite substantially lower estimates of WE emissions for the major ozone precursors – volatile organic compounds (VOC) and oxides of nitrogen (NOx). Compared to WD emissions, WE emissions of NOx decrease more (proportionally) than do the WE emissions of VOC. Because the WE increases in ozone coincide with the relatively large WE reductions in NOx, some conclude that regulations that would reduce NOx emissions on all days would undermine ozone attainment efforts by causing ozone to decrease more slowly (or even to increase). At this time, public discussion of the ozone WE effect has mostly reflected the viewpoint that NOx emission reductions would not help reduce ambient ozone levels. A large body of published research from this perspective has accumulated over the last 10 to 20 years. Nevertheless, the presently available scientific evidence can also lead to the conclusion that NOx emission reductions may be needed to maintain or even to expedite progress toward attainment

Lawrence C. Larsen

2003-01-01T23:59:59.000Z

358

A Statistical Analysis of Total Ozone Data from the Nimbus-4 BUV Satellite Experiment  

Science Conference Proceedings (OSTI)

Total ozone data from the Nimbus-4 BUV satellite experiment for the period April 1970–April 1977 is analyzed to: 1) provide a better appreciation and-understanding of the global distribution and behavior of total ozone, with emphasis on any ...

G. Reinsel; G. C. Tiao; R. Lewis

1982-02-01T23:59:59.000Z

359

Preparation of oxygen-containing organic products from bed-oxidized brown coal by ozonation  

Science Conference Proceedings (OSTI)

The possibility of modifying the functional composition of humic acids by gas-phase ozonation of bed-oxidized brown coal was examined. About 90% of the organic matter of brown coal was converted to low-molecular weight soluble oxygen-containing products by stepwise liquid-phase ozonation (in chloroform and acetic acid).

Semenova, S.A.; Patrakov, Y.F.; Batina, M.V. [National Academy of Science Belarus, Minsk (Byelarus)

2009-01-15T23:59:59.000Z

360

Comparison between the TOPAZ Airborne Ozone Lidar and In Situ Measurements during TexAQS 2006  

Science Conference Proceedings (OSTI)

The NOAA airborne ozone lidar system [Tunable Optical Profiler for Aerosol and Ozone (TOPAZ)] is compared with the fast-response chemiluminescence sensor flown aboard the NOAA WP-3D during the 2006 Texas Air Quality Study (TexAQS). TOPAZ ...

A. O. Langford; C. J. Senff; R. J. Alvarez II; R. M. Banta; R. M. Hardesty; D. D. Parrish; T. B. Ryerson

2011-10-01T23:59:59.000Z

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361

Elevated Ozone Layers over the Seoul Metropolitan Region in Korea: Evidence for Long-Range Ozone Transport from Eastern China and Its Contribution to Surface Concentrations  

Science Conference Proceedings (OSTI)

Elevated layers of high ozone concentration were observed over the Seoul metropolitan region (SMR) in Korea by ozonesonde measurements during 6–9 June 2003. An analysis of the synoptic-scale meteorological features and backward trajectories ...

In-Bo Oh; Yoo-Keun Kim; Mi-Kyung Hwang; Cheol-Hee Kim; Soontae Kim; Sang-Keun Song

2010-02-01T23:59:59.000Z

362

Tropospheric and Lower Stratospheric Ozone Profiles From AERI-X Emission Spectra  

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

Tropospheric and Lower Stratospheric Ozone Profiles Tropospheric and Lower Stratospheric Ozone Profiles From AERI-X Emission Spectra P. F. Fogal and F. J. Murcray Department of Physics and Astronomy University of Denver Denver, Colorado Introduction The University of Denver Atmospheric Emission Radiometric Interferometer-Extended (AERI-X) has been in regular operation at the Southern Great Plains (SGP) Atmospheric Radiation Measurements (ARM) Program site, conditions permitting, since the mid-1990s. We present here the analysis of several spectra from May 10, 1999, and demonstrate the ability to retrieve the tropospheric ozone profile at the ARM site. While the presence of ozone in the stratosphere is of vital importance for several reasons, in the troposphere, ozone is a pollutant and a powerful oxidizer. For these reasons, it is

363

Review of current research on hydrocarbon production by plants  

DOE Green Energy (OSTI)

This review assesses the status of research and development in the area of plants that produce hydrocarbons as a possible replacement for traditional fossil fuels. The information is meant to be used as a basis for determining the scope of a possible R and D program by DOE/FFB. Except in the case of guayule (Parthenium argentatum Gray), research on hydrocarbon species generally has not advanced beyond preliminary screening, extraction, and growth studies. Virtually no field studies have been initiated; hydrocarbon component extraction, separation, identification, and characterization have been only timidly approached; the biochemistry of hydrocarbon formation remains virtually untouched; and potential market analysis has been based on insufficient data. Research interest is increasing in this area, however. Industrial interest understandably centers about guayule prospects and is supplemented by NSF and DOE research funds. Additional support for other research topics has been supplied by DOE and USDA and by certain university systems. Due to the infant state of technology in this area of energy research, it is not possible to predict or satisfactorily assess at this time the potential contribution that plant hydrocarbons might make toward decreasing the nation's dependence upon petroleum. However, the general impression received from experts interviewed during this review was that the major thrust of research should be directed toward the manufacture of petrochemical substitutes rather than fuel production.

Benedict, H. M.; Inman, B.

1979-01-01T23:59:59.000Z

364

Methane-derived hydrocarbons produced under upper-mantle conditions  

SciTech Connect

There is widespread evidence that petroleum originates from biological processes. Whether hydrocarbons can also be produced from abiogenic precursor molecules under the high-pressure, high-temperature conditions characteristic of the upper mantle remains an open question. It has been proposed that hydrocarbons generated in the upper mantle could be transported through deep faults to shallower regions in the Earth's crust, and contribute to petroleum reserves. Here we use in situ Raman spectroscopy in laser-heated diamond anvil cells to monitor the chemical reactivity of methane and ethane under upper-mantle conditions. We show that when methane is exposed to pressures higher than 2 GPa, and to temperatures in the range of 1,000-1,500 K, it partially reacts to form saturated hydrocarbons containing 2-4 carbons (ethane, propane and butane) and molecular hydrogen and graphite. Conversely, exposure of ethane to similar conditions results in the production of methane, suggesting that the synthesis of saturated hydrocarbons is reversible. Our results support the suggestion that hydrocarbons heavier than methane can be produced by abiogenic processes in the upper mantle.

Kolesnikov, Anton; Kutcherov, Vladimir G.; Goncharov, Alexander F.; (CIW); (RITS)

2009-08-13T23:59:59.000Z

365

Variables effecting ozone treatment of physical-chemical effluent  

SciTech Connect

The treatment of raw sewage from an on-site apartment area was investigated in a series of laboratory experiments in which changes in turbidity, pH, total organic carbon, chemical oxygen demand, and, in some cases, biochemical oxygen demands were determined. Raw sewage, but mainly the effluent following physical-chemical treatment, was examined for improvement in discharge quality by ozone treatment in combination with oxygen sparging, ionizing gamma radiation from /sup 60/Co heating, acidifying, and several other variables. The average composition of the raw sewage was a TOC of 125 ppM (range from 65 to 240), COD of 190 ppM (range from 85 to 475), turbidity of 145 J. U. (range from 60 to 350), and pH of 7.3 (range from 6.5 to 8.4). Physical chemical treatment usually consisted of the addition of CaO (to pH 11) and FeCl/sub 3/ as a coagulant aid in an inclined tube followed by course filtration; typical treatment time was 15 minutes giving an average reduction in TOC and COD of 40 to 60%. Subsequent treatment was usually performed with 200 cm/sup 3/ samples of the effluent in fine and course fritted bubblers. The combination of radiation plus ozone gave the largest reduction of TOC and COD. In one experiment, 15 minutes of treatment followed by 30 minutes of irradiation and ozonation reduced the raw sewage TOC from 95 to 14 ppM carbon and COD from 150 to 6 ppM oxygen. (auth)

Dietz, R.N.; Pruzansky, J.; Steinberg, M.

1973-11-01T23:59:59.000Z

366

Toxicity Analysis of Polycyclic Aromatic Hydrocarbon Mixtures  

E-Print Network (OSTI)

Polycyclic aromatic hydrocarbons (PAHs) are widely distributed in the environment and are generated by many sources. Though the potential of PAH-rich mixtures to cause health effects has been known for almost a century, there are still unanswered questions about the levels of PAHs in the environment, the potential for human exposure to PAHs, the health effects associated with exposure, and how genetic susceptibility influences the extent of health effects in individuals. The first objective of this research was to quantify concentrations of PAHs in samples of settled house dust collected from homes in Azerbaijan, China, and Texas. The trends of PAH surface loadings and percentage of carcinogenic PAHs were China > Azerbaijan > Texas, indicating that the risk of health effects from exposure to PAHs in house dust is highest in the Chinese population and lowest in the Texas population. PAHs in China and Azerbaijan were derived mainly from combustion sources; Texas PAHs were derived from unburned fossil fuels such as petroleum. The second objective of this research was to investigate the effect of pregnane X receptor (PXR) on the genotoxicity of benzo[a]pyrene (BaP). BaP treatment resulted in significantly lower DNA adduct levels in PXR-transfected HepG2 cells than in parental HepG2 cells. Total GST enzymatic activity and mRNA levels of several metabolizing enyzmes were significantly higher in cells overexpressing PXR. These results suggest that PXR protects cells against DNA damage by PAHs such as BaP, possibly through a coordinated regulation of genes involved in xenobiotic metabolism. The third objective of this research was to investigate biomarkers of exposure in house mice (Mus musculus) exposed to PAH mixtures in situ. Mice and soil were collected near homes in Sumgayit and Khizi, Azerbaijan. Mean liver adduct levels were significantly higher in Khizi than in Sumgayit. Mean lung and kidney adduct levels were similar in the two regions. The DNA lesions detected may be a combination of environmentally-induced DNA adducts and naturally-occurring I-compounds. PAHs were present at background levels in soils from both Khizi and Sumgayit. It appears that health risks posed to rodents by soil-borne PAHs are low in these two areas.

Naspinski, Christine S.

2009-05-01T23:59:59.000Z

367

Sources of ozone and sulfate in northeastern United States. Annual progress report  

SciTech Connect

Ozone observed at Whiteface Mountain, NY, may be derived from the stratosphere, photochemical production from pollutant NO/sub x/ and hydrocarbons emitted in urban/industrial areas, with subsequent transport of O/sub 3/ to Whiteface Mountain, and/or photochemical production from NO/sub x/ and hyodrocarbons including terpenes, etc., emitted from vegetation in the vicinity of Whiteface Mountain. The principal objective of this work was to assess /sup 7/Be and /sup 32/P as stratospheric tracers and, if possible, use them to quantify stratospheric O/sub 3/. Other objectives of this program were: to study the relationship between O/sub 3/ and SO/sub 4//sup 2 -/, use SO/sub 4//sup 2 -/ as an indicator of photochemical production originating in urban areas, to study the long-range transport of pollutants and try to identify emission sources and establish daily, monthly, and seasonal variations of SO/sub 4//sup 2 -/ and trace elements thus generating a data base to study long-term trends. The salient features of this study were the first determinations of /sup 7/Be/O/sub 3/ ratios in the lower stratosphere and upper troposphere and gathering continuous data of radionuclides /sup 7/Be, /sup 32/P, and /sup 33/P along with O/sub 3/, SO/sub 4//sup 2 -/, and several trace elements. Some of the significant accomplishments of this study are: a quantitative relationships between /sup 7/Be and O/sub 3/ in the stratosphere was established, and it is applied to estimate stratospheric O/sub 3/ on a global and episodic basis; global /sup 7/Be measurements suggest that the stratospheric influx in the northern hemisphere is twice that in the southern; and, the /sup 7/Be//sup 32/P ratios yield an average transport time of approx. 7 days during spring and summer for stratospheric air from tropopause to Whiteface Mountain, supporting tropopause folding as the predominant mechanism of stratospheric-tropospheric exchange during spring and summer. (JGB)

Husain, L.

1980-06-30T23:59:59.000Z

368

Isolation and characterization of five ozone-inductible cDNA clones from Atriplax canescens (saltbush)  

E-Print Network (OSTI)

Prolonged exposure of plants to ozone inhibits growth and development and produces visible signs of damage. Within a few hours of exposure, certain biochemical alterations have been observed with the induction of several stress-related proteins. accumulation of several polya RNAS. CDNA clones derived from five different polya RNAs which accumulate in ozone-stressed shrub leaves were isolated by differential screening methods. Alteration in gene expression which occurs with ozone, sulfur dioxide and water deficit were examined, and those cDNAs were sequenced. Clone 012-1, hybridized with three RNA species, is initially induced in response to both ozone and water deficit stress, but is repressed to prolonged ozone and sulfur dioxide exposure. Clone 012-1 has strong homology with small subunit RRNA. Northern blots suggest that transcripts hybridized to 012-1 are a naked species (about 1.45 kb) and are subfragments (1.0 and 0.45 kb) of 1.4 kb species. 0112A-3 showed an increase in response to two pollutants, but not to water deficit. 0112A-3 encodes a polypeptide which has homology with wound-inducible protein inhibitors. MRNA species corresponding to 018-3 are transiently induced in response to sulfur dioxide and water deficit stress, and are late-induced by ozone stress. The 018-3 protein is Ozone fumigation to Atriplex canescens (saltbush) caused the homologous to thiol proteases. Clone OID2-2 and OIS14-3 show similar patterns in gene expression Transcript levels of the two genes rise rapidly and remain at a high level by seven days after ozone fumigation, and rise steadily in response to water deficit and sulfur dioxide stress. The deduced amino acids of both clones are glycine-rich proteins, and they have repeated motifs, (G-G-G-Y-G-H)n, and putative cell wall-targeting signal peptides. Northern analyses indicate that plant cells respond to ozone stress by increasing transcription of several genes. Furthermore, the expression of ozone-inducible genes varies with respect to the time course of induction and different stresses such as water-deficit and sulfur dioxide stress. The encoded proteins suggest that: first, ozone stress may generate wounding damage to increase the expression of the proteinase inhibitor (0112A-3) and the protease (018-3); second, ozone stress may change the cell wall components by increasing the amount of glycine-rich proteins (OID2-2 and OIS14-3); and third, ozone stress may change the cell wall structure with tyrosine-mediated cross-linking, which may use oxyradical-scavenging effects to relieve cellular stress.

No, Eun-Gyu

1994-01-01T23:59:59.000Z

369

Catalytic Upgrading of Sugars to Hydrocarbons Technology Pathway  

Science Conference Proceedings (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

370

Method and apparatus for producing oxygenates from hydrocarbons  

DOE Patents (OSTI)

A chemical reactor for oxygenating hydrocarbons includes: a) a dielectric barrier discharge plasma cell, the plasma cell comprising a pair of electrodes having a dielectric material and void therebetween, the plasma cell comprising a hydrocarbon gas inlet feeding to the void; b) a solid oxide electrochemical cell, the electrochemical cell comprising a solid oxide electrolyte positioned between a porous cathode and a porous anode, an oxygen containing gas inlet stream feeding to the porous cathode side of the electrochemical cell; c) a first gas passageway feeding from the void to the anode side of the electrochemical cell; and d) a gas outlet feeding from the anode side of the electrochemical cell to expel reaction products from the chemical reactor. A method of oxygenating hydrocarbons is also disclosed.

Kong, Peter C. (Idaho Falls, ID); Lessing, Paul A. (Idaho Falls, ID)

1995-01-01T23:59:59.000Z

371

Catalytic Fast Pyrolysis for the Production of the Hydrocarbon Biofuels  

SciTech Connect

Catalytic fast pyrolysis is a promising technique for conversion of biomass into hydrocarbons for use as transportation fuels. For over 30 years this process has been studied and it has been demonstrated that oils can be produced with high concentrations of hydrocarbons and low levels of oxygen. However, the yields from this type of conversion are typically low and the catalysts, which are often zeolites, are quickly deactivated through coking. In addition, the hydrocarbons produced are primarily aromatic molecules (benzene, toluene, xylene) that not desirable for petroleum refineries and are not well suited for diesel or jet engines. The goals of our research are to develop new multifunction catalysts for the production of gasoline, diesel and jet fuel range molecules and to improve process conditions for higher yields and low coking rates. We are investigating filtration and the use of hydrogen donor molecules to improve catalyst performance.

Nimlos, M. R.; Robichaud, D. J.; Mukaratate, C.; Donohoe, B. S.; Iisa, K.

2013-01-01T23:59:59.000Z

372

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. 1 fig. 2 tab.

Shelnutt, J.A.

1989-09-26T23:59:59.000Z

373

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

374

Reclamation and reuse of Freon in total petroleum hydrocarbon analyses  

Science Conference Proceedings (OSTI)

At the Savannah River Technology Center (SRTC), we have successfully demonstrated the use of a solvent recycling system to reclaim spent Freon solvent in total petroleum hydrocarbon (TPH) analyses of radioactive samples. A wide variety of sample types including ground water, organics, laboratory waste, process control, sludge, soils, and others are received by our lab for total petroleum hydrocarbon analysis. This paper demonstrates the successful use of a commercially available carbon bed recycle system which we modified to enable the recovery of 95-98 percent of the radioactive contaminated Freon. This system has been used successfully in our lab for the past three years.

Ekechukwu, A.A.; Young, J.E.

1997-12-31T23:59:59.000Z

375

Method and apparatus for synthesizing various short chain hydrocarbons  

DOE Patents (OSTI)

A method and apparatus, 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 are fluidized in a fluidized-bed reactor having a transparent window, by hydrogen and CO, C{sub 2}H{sub 4} or C{sub 2}H{sub 6} gas mixtures, and exposed to radiation from a light source external to the reactor, to produce the short chain hydrocarbons. 1 fig., 1 tab.

Colmenares, C.

1989-05-05T23:59:59.000Z

376

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

377

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

378

Preliminary investigation of the nature of hydrocarbon migration and entrapment  

E-Print Network (OSTI)

Numerical simulations indicate that hydrocarbon migration and entrapment in stacked fault-bounded reservoirs are mainly affected by the following factors: charge time, faults, pressure and geological 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 hydrocarbon percent charge and hydrocarbon migration pathways. Updip back doors improve updip oil charge. The lower the displacement pressure of an updip back door, the more efficient the updip oil charge before 3,000 years. Back doors whose displacement pressure is equal to or higher than 28.76 psi are effective in sealing faults in oil-water systems. On the contrary, only sealing faults result in commercial gas accumulations in stacked fault-compartmentalized reservoirs. Otherwise gas is found over oil. Downdip back doors generally have few effects on downdip hydrocarbon charge. Geopressure enhances the updip oil transportation of a fault and improves the positive effects of updip back doors during updip oil charge. Geopressure and updip back doors result in more efficient updip oil charge. A physical barrier is not necessarily a barrier to oil migration with the aid of geopressure and updip back doors. The chance for hydrocarbon charge into reservoirs along growth faults is not equal. Any one of the above controlling factors can change the patterns of hydrocarbon charge and distribution in such complex geological structures. Generally, lower reservoirs and updip reservoirs are favored. Reservoirs along low-permeability charging faults may be bypassed. Gas can only charge the updip reservoirs. Both updip and downdip back doors can facilitate oil penetrating a barrier fault to charge reservoirs offset by the barrier fault. Interreservoir migration among stacked fault-compartmentalized reservoirs is an important mechanism for hydrocarbon accumulation and trap identification. The interreservoir migration is a very slow process, even though the displacement pressures of bounding faults may be very low.

Bai, Jianyong

2005-05-01T23:59:59.000Z

379

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

380

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

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

Ozone-depleting-substance control and phase-out plan  

SciTech Connect

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

382

Future aircraft and potential effects on stratospheric ozone and climate  

Science Conference Proceedings (OSTI)

The purpose of this study is to extend the recent research examining the global environmental effects from potential fleets of subsonic and supersonic commercial aircraft. Initial studies with LLNL models of global atmospheric chemical, radiative, and transport processes have indicated that substantial decreases in stratospheric ozone concentrations could result from emissions of NO{sub x} from aircraft flying in the stratosphere, depending on fleet size and magnitude of the engine emissions. These studies used homogeneous chemical reaction rates (e.g. gas-phase chemistry). Recent evidence indicates that reactions on particles in the stratosphere may be important. Heterogeneous chemical reactions, for instance, N{sub 2}O{sub 5}and ClONO{sub 2} on background sulfuric acid aerosols, convert NO{sub x}(NO and NO{sub 2}) molecules to HNO{sub 3}. This decreases the odd oxygen loss from the NO{sub x} catalytic cycle and increases the odd oxygen loss from the Cl{sub x} catalytic cycle. By including these heterogeneous reactions in the LLNL model, the relative partitioning of odd oxygen loss between these two families changes, with the result that emissions of NO{sub x} from proposed aircraft fleets flying in the stratosphere now increase zone. Having these heterogeneous processes present also increases ozone concentration in the troposphere relative to gas-phase only chemistry calculations for emissions of NO{sub x} from subsonic aircraft. 26 refs., 5 figs., 3 tabs.

Kinnison, D.E.; Wuebbles, D.J.

1991-10-01T23:59:59.000Z

383

Imaging Spectrometry of Tropospheric Ozone and Water Vapor  

E-Print Network (OSTI)

Imaging spectrometry has the potential of remotely detecting atmospheric trace gases on the basis of their absorption of radiation. Ozone absorbs particulary in the ultraviolet and visible range of the spectrum, whereas water vapor has strong absorption features in the near infrared. Hence, spectrometry is expected to be a promising tool to extract these trace gas contents in a given air column by using the correlation between cumulative trace gas amount and absorption strength in the sensor channels located in the absorption bands. New mathematical methods of channel selection and method evaluation for measuring atmospheric trace gases are presented. Three already known and four new differential absorption techniques are evaluated by using MODTRAN2 simulations of the radiance spectrum at the sensor level and an analytical error propagation analysis. Finally, the best methods and channel combinations are selected and applied to AVIRIS data of Central Switzerland. The spatial ozone distribution could be estimated over water in a qualitative manner, whereas the total column water vapor content could be quantified over land with an accuracy of about 6%.

Daniel Schläpfer; Klaus I. Itten; Johannes Keller

1995-01-01T23:59:59.000Z

384

Sensitivity analysis of ozone formation and transport for a Central California air pollution episode  

SciTech Connect

CMAQ-HDDM is used to determine spatial and temporal variations in ozone limiting reagents and local vs upwind source contributions for an air pollution episode in Central California. We developed a first- and second- order sensitivity analysis approach with the Decoupled Direct Method to examine spatial and temporal variations of ozone-limiting reagents and the importance of local vs upwind emission sources in the San Joaquin Valley of central California for a five-day ozone episode (29th July-3rd Aug, 2000). Despite considerable spatial variations, nitrogen oxides (NO{sub x}) emission reductions are overall more effective than volatile organic compound (VOC) control for attaining the 8-hr ozone standard in this region for this episode, in contrast to the VOC control that works better for attaining the prior 1-hr ozone standard. Inter-basin source contributions of NO{sub x} emissions are limited to the northern part of the SJV, while anthropogenic VOC (AVOC) emissions, especially those emitted at night, influence ozone formation in the SJV further downwind. Among model input parameters studied here, uncertainties in emissions of NO{sub x} and AVOC, and the rate coefficient of the OH + NO{sub 2} termination reaction, have the greatest effect on first-order ozone responses to changes in NO{sub x} emissions. Uncertainties in biogenic VOC emissions only have a modest effect because they are generally not collocated with anthropogenic sources in this region.

Jin, Ling; Tonse, Shaheen; Cohan, Daniel S.; Mao, Xiaoling; Harley, Robert A.; Brown, Nancy J.

2009-05-15T23:59:59.000Z

385

Variability of Gas Composition and Flux Intensity in Natural Marine Hydrocarbon Seeps  

E-Print Network (OSTI)

Energy Development and Technology 008 "Variability of gas composition and flux intensity in natural marine hydrocarbon seeps" Jordan

Clark, J F; Schwager, Katherine; Washburn, Libe

2005-01-01T23:59:59.000Z

386

Hydrocarbon compositions of high elongational viscosity and process for making the same  

SciTech Connect

A hydrocarbon composition is described consisting essentially of a hydrocarbon liquid and an ionic-association or coordination-complex polymer in an amount sufficient to increase and maintain the elongational viscosity of the composition at a level greater than that of the hydrocarbon alone. The polymer is capable of dissociation upon application of the high shear regime to which the hydrocarbon is subjected, and reassociation upon withdrawal of the high shear.

Hamil, H.F.; Weatherford, W.D. Jr.; Fodor, G.E.

1988-03-15T23:59:59.000Z

387

U.S. Product Supplied of Other Hydrocarbons/Oxygenates (Thousand ...  

U.S. Energy Information Administration (EIA)

Product Supplied for Hydrogen/Oxygenates/Renewables/Other Hydrocarbons ; U.S. Product Supplied for Crude Oil and Petroleum Products ...

388

U.S. Exports of Other Hydrocarbons/Oxygenates (Thousand Barrels ...  

U.S. Energy Information Administration (EIA)

Hydrogen/Oxygenates/Renewables/Other Hydrocarbons Supply and Disposition; U.S. Exports of Crude Oil and Petroleum Products ...

389

Recovery of normally gaseous hydrocarbons from net excess hydrogen in a catalytic reforming process  

Science Conference Proceedings (OSTI)

A process is disclosed for the catalytic reforming of hydrocarbons in the presence of hydrogen, preferably to produce high quality gasoline boiling range products. An improved recovery of normally gaseous hydrocarbons from the net excess hydrogen is realized by chilling and contacting said hydrogen with a normally liquid hydrocarbon stream in a plural stage absorption zone at an elevated pressure.

Scheifele, C.A.

1982-06-08T23:59:59.000Z

390

THERMOCATALYTIC CO2-FREE PRODUCTION OF HYDROGEN FROM HYDROCARBON FUELS  

E-Print Network (OSTI)

, preferential oxidation) and gas separation stages required by conventional technologies (e.g., steam reforming and carbon via sustainable catalytic decomposition of methane or other hydrocarbons using inexpensive-situ generation of catalytically active carbon species produced by co-decomposition of methane and unsaturated and

391

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, indene, azulene, fluorene, and biphenyl substituted compounds. Also, lighter hydrocarbons, such as ethylene and isobutene were produced. The reaction was conducted at different operating temperatures and different molar feed composition. The results showed that the conversion of both reactants increased with increasing the operating temperature; for example a conversion of 95.1% was achieved for acetylene at 350°C and 98.6% at 412°C. In addition, the conversion of both reactants decreased with increasing the molar feed ratio of methane to acetylene. A conversion of 96.4% for acetylene was achieved at a molar feed ratio of 6 to 1 (methane to acetylene) and 80.9% at a molar feed ration of 20 to 1 (methane to acetylene). The reaction of methane and ethane over HZSM-5 catalyst also led to the production of high molecular weight hydrocarbons, mainly aromatics, and some lighter products such as propane, and ethylene. Also methane by itself showed the ability to react over HZSM-5 to produce a small amount of aromatics, and ethylene.

Alkhawaldeh, Ammar

2000-01-01T23:59:59.000Z

392

Source Contributions to VOC's to Ozone Formation in Southeast Texas Using a Source-oriented Air Quality Model  

E-Print Network (OSTI)

Houston-Galveston-Brazoria area is in severe non-attainment status for ozone compliance. Source-oriented mechanistic modeling was used to determine the major sources of VOCs that contributes to ozone formation during the Texas Air Quality Study (TexAQS) from August 16, 2000 to September 7, 2000. Environmental Protection Agency (EPA)?s Community Scale Air Quality Model (CMAQ) version 4.6 was used as a host model to include a revised Statewide Air Pollution Research Center (SAPRC99) photochemical mechanism with source-oriented extensions to track the contributions of Volatile Organic Compounds (VOCs) emissions from diesel engines, biogenic sources, highway gasoline vehicles, fuel combustion, off-highway gasoline engines, solvent utilization and petrochemical industries to ozone formation in the atmosphere. Source-oriented emissions needed to drive the model were generated using a revised Sparse Matrix Operator Kernel Emissions (SMOKE) model version 2.4. VOC/NOx ratios are found to be a critical factor in the formation of ozone. Highest ozone formation rates were observed for ratios from 5-15. The contributions of VOC to ozone formation were estimated based on the linear relationship between the rate of NO to NO2 conversion due to radicals generated from VOC oxidation and the rate of net ozone formation. Petroleum and other industrial sources are the largest anthropogenic sources in the urban Houston region and contribute to 45% of the ozone formation in the HGB area. Highway gasoline vehicles make contributions of approximately 28% to ozone formation. Wildfires contribute to as much 11% of ozone formation on days of high wildfire activity. The model results show that biogenic emissions account for a significant amount of ozone formation in the rural areas. Both highway and off-highway vehicles contribute significantly to ozone formation especially in the downwind region. Diesel vehicles do not contribute significantly to ozone formation due to their low VOC emissions.

Krishnan, Anupama

2010-05-01T23:59:59.000Z

393

Method for producing hydrocarbon fuels and fuel gas from heavy polynuclear hydrocarbons by the use of molten metal halide catalysts  

DOE Patents (OSTI)

In a process for hydrocracking heavy polynuclear carbonaceous feedstocks to produce lighter hydrocarbon fuels by contacting the heavy feedstocks with hydrogen in the presence of a molten metal halide catalyst in a hydrocracking zone, thereafter separating at least a major portion of the lighter hydrocarbon fuels from the spent molten metal halide and thereafter regenerating the spent molten metal halide by incinerating the spent molten metal halide by combustion of carbon and sulfur compounds in the spent molten metal halide in an incineration zone, the improvement comprising: (a) contacting the heavy feedstocks and hydrogen in the presence of the molten metal halide in the hydrocracking zone at reaction conditions effective to convert from about 60 to about 90 weight percent of the feedstock to lighter hydrocarbon fuels; (b) separating at least a major portion of the lighter hydrocarbon fuels from the spent molten metal halide; (c) contacting the spent molten metal halide with oxygen in a liquid phase gasification zone at a temperature and pressure sufficient to vaporize from about 25 to about 75 weight percent of the spent metal halide, the oxygen being introduced in an amount sufficient to remove from about 60 to about 90 weight percent of the carbon contained in the spent molten metal halide to produce a fuel gas and regenerated metal halide; and (d) incinerating the spent molten metal halide by combusting carbon and sulfur compounds contained therein.

Gorin, Everett (San Rafael, CA)

1979-01-01T23:59:59.000Z

394

Influence of Long-Period Variations of Total Ozone Content on Climate  

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

Influence of Long-Period Variations of Total Ozone Content on Climate Influence of Long-Period Variations of Total Ozone Content on Climate Change in Twentieth Century Zuev, V Institute of Atmospheric Optics Zueva, N. Institute of Atmospheric Optics Bondarenko, S Institute of Atmospheric Optics Category: Atmospheric State and Surface It is shown that during long-term total ozone decrease everywhere at middle and high latitudes there takes place the destruction of balance in global carbon cycle first of all due to reduction of photosynthetical СО2 sink in consequence of UV-B radiation stress of vegetable biota. As a result, СО2 concentrations in the atmosphere considerably increase, enhancing the "greenhouse effect." Based on reconstruction of behavior of stratospheric ozone between 1600 and 2000 from dendrochronologic data, it is shown that

395

Upper-Level Atmospheric Circulation Patterns and Ground-Level Ozone in the Atlanta Metropolitan Area  

Science Conference Proceedings (OSTI)

The purpose of this paper is to identify middle-troposphere circulation patterns associated with high ozone concentrations during June–August of 2000–07 in the Atlanta, Georgia, metropolitan statistical area (MSA), which is located in the ...

Jeremy E. Diem; Melissa A. Hursey; Imani R. Morris; Amanda C. Murray; Ricardo A. Rodriguez

2010-11-01T23:59:59.000Z

396

An Estimation of the Climatic Effects of Stratospheric Ozone Losses during the 1980s  

Science Conference Proceedings (OSTI)

In order to study the potential climatic effects of the ozone hole more directly and to assess the validity of previous lower resolution model results, the latest high spatial resolution version of the Atmospheric and Environmental Research, Inc.,...

Robert M. MacKay; Malcolm K. W. Ko; Run-Lie Shia; Yajaing Yang; Shuntai Zhou; Gyula Molnar

1997-04-01T23:59:59.000Z

397

UV Sensitivity to Changes in Ozone, Aerosols and Clouds in Seoul, Korea  

Science Conference Proceedings (OSTI)

The total ozone (O3) and aerosol optical depth (AOD) at 320 nm have been observed from the ultraviolet (UV) measurements made at Yonsei University in Seoul, Korea with Dobson and Brewer spectrophotometers, respectively, during 2004-2010. The daily ...

Woogyung Kim; Jhoon Kim; Sang Seo Park; Hi-Ku Cho

398

A Two-Dimensional Model of the Quasi-biennial Oscillation of Ozone  

Science Conference Proceedings (OSTI)

The stratospheric quasi-biennial oscillation (QBO) in zonal wind, temperature and column ozone has been successfully modeled in a two-dimensional dynamical/chemical model by the introduction of a parameterization scheme to model the transfer of ...

L. J. Gray; J. A. Pyle

1989-01-01T23:59:59.000Z

399

Greenhouse gases and future long-term changes in the stratospheric temperature and the ozone layer  

Science Conference Proceedings (OSTI)

A numerical two-dimensional (2D) interactive dynamical-radiative-photochemical model including aerosol physics is used to examine the expected long-term changes in stratospheric temperature and the Earth's ozone layer due to anthropogenic pollution of ...

I. G. Dyominov; A. M. Zadorozhny

2008-05-01T23:59:59.000Z

400

Separating the Dynamical Effects of Climate Change and Ozone Depletion. Part II: Southern Hemisphere Troposphere  

Science Conference Proceedings (OSTI)

The separate effects of ozone depleting substances (ODSs) and greenhouse gases (GHGs) on forcing circulation changes in the Southern Hemisphere extratropical troposphere are investigated using a version of the Canadian Middle Atmosphere Model (...

Charles McLandress; Theodore G. Shepherd; John F. Scinocca; David A. Plummer; Michael Sigmond; Andreas I. Jonsson; M. Catherine Reader

2011-03-01T23:59:59.000Z

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.


401

Calculated Influence of Temperature-Related Factors on Ozone Formation Rates in the Lower Troposphere  

Science Conference Proceedings (OSTI)

Using an atmospheric chemical reaction mechanism applied to air parcels near the earth's surface, the sensitivities ozone (O3) formation rates are quantified for changes in four meteorologically controlled parameters: temperature, sunlight ...

Chris J. Walcek; Hong-H. Yuan

1995-05-01T23:59:59.000Z

402

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

E-Print Network (OSTI)

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

Aydogan, Ahmet

2006-01-01T23:59:59.000Z

403

Interannual Variations of Total Ozone and Their Relationship to Variations of Planetary Wave Activity  

Science Conference Proceedings (OSTI)

Interannual variations of total ozone at midlatitudes of the Northern Hemisphere are shown to operate coherently with variations of upwelling planetary wave activity from the troposphere. Variations of upwelling wave activity, which modulate ...

Andrew C. Fusco; Murry L. Salby

1999-06-01T23:59:59.000Z

404

An Automated Classification Scheme Designed to Better Elucidate the Dependence of Ozone on Meteorology  

Science Conference Proceedings (OSTI)

This paper utilizes a two-stage (average linkage then convergent k means) clustering approach as part of an automated meteorological classification scheme designed to better elucidate the dependence of ozone on meteorology. When applied to 10 ...

Brian K. Eder; Jerry M. Davis; Peter Bloomfield

1994-10-01T23:59:59.000Z

405

Short-Range Prediction of Tropospheric Ozone Concentrations and Exceedances for Baton Rouge, Louisiana  

Science Conference Proceedings (OSTI)

Previous research has been focused on improving forecasts of the daily maximum 1-h concentration of tropospheric ozone, which was based on criteria used by the U.S. Environmental Protection Agency (EPA). However, in 2001, EPA began implementing ...

Robert V. Rohli; S. A. Hsu; Brian W. Blanchard; R. L. Fontenot

2003-04-01T23:59:59.000Z

406

Mesoscale Meteorological Structure of a High-Ozone Episode during the 1995 NARSTO-Northeast Study  

Science Conference Proceedings (OSTI)

Observations and numerical model fields were analyzed to study the meteorological structures contributing to high concentrations of lower-tropospheric ozone over the northeastern United States on 14–15 July 1995. It was found that the episode is ...

Nelson L. Seaman; Sara A. Michelson

2000-03-01T23:59:59.000Z

407

Trends in Stratospheric Ozone: Lessons Learned from a 3D Chemical Transport Model  

Science Conference Proceedings (OSTI)

Stratospheric ozone is affected by external factors such as chlorofluorcarbons (CFCs), volcanoes, and the 11-yr solar cycle variation of ultraviolet radiation. Dynamical variability due to the quasi-biennial oscillation and other factors also ...

Richard S. Stolarski; Anne R. Douglass; Stephen Steenrod; Steven Pawson

2006-03-01T23:59:59.000Z

408

Missing Stratospheric Ozone Decrease at Southern Hemisphere Middle Latitudes after Mt. Pinatubo: A Dynamical Perspective  

Science Conference Proceedings (OSTI)

Although large total ozone decreases occurred in the Northern Hemisphere extratropics in the years after the volcanic eruption of Mt. Pinatubo that are generally attributed to the eruption, comparable decreases did not emerge in the Southern ...

C. Schnadt Poberaj; J. Staehelin; D. Brunner

2011-09-01T23:59:59.000Z

409

Modeling Ozone Formation and Transport in the Cascadia Region of the Pacific Northwest  

Science Conference Proceedings (OSTI)

The rapidly growing Cascadia region of the Pacific Northwest, consisting of western Washington, Oregon, and southwestern British Columbia, has experienced surface ozone concentrations that exceed federally mandated standards. A modeling system ...

Mike Barna; Brian Lamb; Susan O’Neill; Hal Westberg; Cris Figueroa-Kaminsky; Sally Otterson; Clint Bowman; Jennifer DeMay

2000-03-01T23:59:59.000Z

410

Estimating changes in urban ozone concentrations due to life cycle emissions from hydrogen transportation systems  

E-Print Network (OSTI)

criteria.htmlS. Accessed on NRC, 1991. Rethinking the OzonePress, Washington, DC. NRC, 2004. The Hydrogen Economy:hours of the summer months (NRC, 1991). In summary the ‘‘

Wang, Guihua; Ogden, Joan M; Chang, Daniel P.Y.

2007-01-01T23:59:59.000Z

411

Modeling the Effect of Chlorine Emissions on Ozone Levels over the Eastern United States  

Science Conference Proceedings (OSTI)

This paper presents model estimates of the effect of chlorine emissions on atmospheric ozone concentrations in the eastern United States. The model included anthropogenic molecular chlorine emissions, anthropogenic hypochlorous acid emissions ...

Golam Sarwar; Prakash V. Bhave

2007-07-01T23:59:59.000Z

412

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

413

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

414

Trends in ozone and temperature structure: comparison of theory and measurements  

Science Conference Proceedings (OSTI)

Comparison of model calculated trends in ozone and temperature due to inferred variations in trace gas concentrations and solar flux, is made with available analyses of observations. In general, the calculated trends in total ozone and the vertical ozone distribution agree well with the measured trends. However, there are too many remaining theoretical and sampling uncertainties to establish causality. Although qualitatively in agreement, the observed temperature decrease in the upper stratosphere is significantly larger than that calculated. Theoretical results suggest a significant influence on stratospheric ozone from solar flux variations, but observational evidence is at best inconclusive. Overall, the trend comparisons tend to be consistent with the hypothesis that several different anthropogenic influences are affecting the present global atmosphere. 7 references, 3 figures, 2 tables.

Wuebbles, D.J.

1984-08-01T23:59:59.000Z

415

The Characterization of an Air Pollution Episode Using Satellite Total Ozone Measurements  

Science Conference Proceedings (OSTI)

A case study is presented which demonstrates that measurements of total ozone from a space platform can be used to study a widespread air pollution episode over the southeastern United States. In particular the synoptic-scale distribution of ...

Jack Fishman; Fred M. Vukovich; Donald R. Cahoon; Mark C. Shipham

1987-12-01T23:59:59.000Z

416

Characterization of the Nimbus-7 SBUV Radiometer for the Long-Term Monitoring of Stratospheric Ozone  

Science Conference Proceedings (OSTI)

Precise knowledge of in-orbit sensitivity change is critical for the successful monitoring of stratosphere ozone by satellite-based remote sensors. This paper evaluates those aspects of the in-flight operation that influence the long-term ...

R. P. Cebula; H. Park; D. F. Heath

1988-04-01T23:59:59.000Z

417

Global Normal-Mode Rossby Waves Observed in Stratospheric Ozone Data  

Science Conference Proceedings (OSTI)

Westward-propagating Rossby normal-mode planetary waves are documented in stratospheric ozone data using Solar Backscatter Ultraviolet (SBUV) satellite measurements. These modes are evidenced by enhanced spectral power and near-global coherence ...

William J. Randel

1993-02-01T23:59:59.000Z

418

The Long-Term Coupling between Column Ozone and Tropopause Properties  

Science Conference Proceedings (OSTI)

The observational data of the vertical temperature distribution and column ozone, obtained from 10 main stations in the Northern Hemisphere, are analyzed in order to explore the tropopause variations in conjunction with the dynamical variability ...

Costas Varotsos; Costas Cartalis; Andrew Vlamakis; Chris Tzanis; Iphigenia Keramitsoglou

2004-10-01T23:59:59.000Z

419

Ground-level ozone in eastern North America : its formation and transport  

E-Print Network (OSTI)

Ozone (Os), a natural component of the troposphere, is augmented by photochemical processes involving manmade emissions of nitrogen oxides (NOx) and volatile organic compounds (VOCs). Sufficiently high concentrations of ...

Zemba, Stephen G.

1990-01-01T23:59:59.000Z

420

A Novel Lightweight Low-Power Dual-Beam Ozone Photometer Utilizing Solid-State Optoelectronics  

Science Conference Proceedings (OSTI)

Recent advances in semiconductor materials and fabrication techniques have allowed the development of light-emitting diodes (LEDs) with wavelengths extending down into the UV-C region (? < 280 nm). A new ozone photometer has been developed ...

Lars E. Kalnajs; Linnea M. Avallone

2010-05-01T23:59:59.000Z

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.


421

Stratospheric Ozone Decrease Due to Chlorofluoromethane Photolysis: Predictions of Latitude Dependence  

Science Conference Proceedings (OSTI)

A two-dimensional model is used to predict the 1990 reduction in ozone due to the chlorine compounds formed by chlorofluoromethane (CFM) photolysis when the CFM release rate is held constant at the 1975 value. The predicted globally averaged ...

W. J. Borucki; R. C. Whitten; H. T. Woodward; L. A. Capone; C. A. Riegel; S. Gaines

1980-03-01T23:59:59.000Z

422

An Approach to the Detection of Long-Term Trends in Upper Stratospheric Ozone from Space  

Science Conference Proceedings (OSTI)

A central problem in the detection of long-term trends in upper stratospheric ozone from orbiting remote sensors involves the separation of instrument drifts from true geophysical changes. Periodic flights of a Solar Backscatter Ultraviolet ...

John E. Frederick; Xufeng Niu; Ernest Hilsenrath

1990-10-01T23:59:59.000Z

423

Ozone Cycles in the Western Mediterranean Basin: Interpretation of Monitoring Data in Complex Coastal Terrain  

Science Conference Proceedings (OSTI)

In summer, the complex layout of the coasts and mountains surrounding the western Mediterranean basin favors the development of mesoscale atmospheric recirculations and the formation of ozone reservoir layers above the coastal areas and the sea. ...

Millán M. Millán; Enrique Mantilla; Rosa Salvador; Adoración Carratalá; Maria José Sanz; Lucio Alonso; Gotzon Gangoiti; Marino Navazo

2000-04-01T23:59:59.000Z

424

Evaluation of an Improved Set of Predictors for Derivation of Total Ozone from TOVS Measurements  

Science Conference Proceedings (OSTI)

Three improvements to the operational regression procedures used at NOAA/NESDIS to derive total ozone from the TIROS Operational Vertical Sounder (TOVS) measurements are evaluated. An additional predictor, derived from the TOVS measurements, is ...

James H. Lienesch

1988-10-01T23:59:59.000Z

425

Dynamical Response of the Tropical Total Ozone to Sea Surface Temperature Changes  

Science Conference Proceedings (OSTI)

Interannual variations of total ozone in the equatorial region are discussed in terms of the lower-stratospheric dynamical processes associated with sea surface temperature (SST) changes on an EJ Niño-Southern Oscillation time scale. Tropospheric ...

Fumio Hasebe

1993-02-01T23:59:59.000Z

426

Interannual Variability and Trends of Extratropical Ozone. Part II: Southern Hemisphere  

Science Conference Proceedings (OSTI)

A principal component analysis (PCA) is applied to the Southern Hemisphere (SH) total column ozone following the method established for analyzing the data in the Northern Hemisphere (NH) in a companion paper. The interannual variability (IAV) of ...

Xun Jiang; Steven Pawson; Charles D. Camp; J. Eric Nielsen; Run-Lie Shia; Ting Liao; Varavut Limpasuvan; Yuk L. Yung

2008-10-01T23:59:59.000Z

427

The Ozone Hole Breakup in September 2002 as Seen by SCIAMACHY on ENVISAT  

Science Conference Proceedings (OSTI)

An unprecedented stratospheric warming in the Southern Hemisphere in September 2002 led to the breakup of the Antarctic ozone hole into two parts. The Scanning Imaging Absorption Spectrometer for Atmospheric Chartography (SCIAMACHY) on the ...

C. von Savigny; A. Rozanov; H. Bovensmann; K.-U. Eichmann; S. Noël; V. Rozanov; B.-M. Sinnhuber; M. Weber; J. P. Burrows; J. W. Kaiser

2005-03-01T23:59:59.000Z

428

Stratospheric Sensitivity to Perturbations in Ozone and Carbon Dioxide: Radiative and Dynamical Response  

Science Conference Proceedings (OSTI)

We have attempted to assess the stratospheric effects of two different perturbations: 1) a uniform 50% reduction in ozone; and 2) a uniform doubling of carbon dioxide. The primary studies employ an annual mean insulation version of the recently ...

S. B. Fels; J. D. Mahlman; M. D. Schwarzkopf; R. W. Sinclair

1980-10-01T23:59:59.000Z

429

Remote Sensing Measurements of Tropospheric Ozone by Ground-Based Thermal Emission Spectroscopy  

Science Conference Proceedings (OSTI)

Remote sensing measurements of the troposphere were obtained by a new technique in which spectra of the downward thermal radiation from tropospheric ozone were measured with a Fourier transform infrared spectrometer. The measurements were ...

W. F. J. Evans; E. Puckrin

1999-01-01T23:59:59.000Z

430

A Chemiluminescent Analyzer for Stratospheric Measurements of the Ozone Concentration (FOZAN)  

Science Conference Proceedings (OSTI)

Within the framework of the Airborne Polar Experiment, a new ozone analyzer based on chemiluminescent technology has been developed for high-altitude measurements. The instrument was tested on board the M-55 Geophysica aircraft during some ...

V. Yushkov; A. Oulanovsky; N. Lechenuk; I. Roudakov; K. Arshinov; F. Tikhonov; L. Stefanutti; F. Ravegnani; U. Bonafé; T. Georgiadis

1999-10-01T23:59:59.000Z

431

Ozone Loss and Recovery and the Preconditioning of Upward Propagating Planetary Wave Activity  

Science Conference Proceedings (OSTI)

A mechanistic chemistry-dynamical model is used to evaluate the relative importance of radiative, photochemical, and dynamical feedbacks in communicating changes in lower stratospheric ozone to the circulation of the stratosphere and lower ...

John R. Albers; Terrence R. Nathan

432

Global distributions of total ozone during January and February 1979 as determined from DMSP multichannel filter radiometer measurements  

Science Conference Proceedings (OSTI)

The multichannel filter radiometer instrument (MFR) was first flown on a Defense Meteorological Satellite Program (DMSP) Block 5D series satellite in 1977. Daily analyses of the global distribution of retrieved total ozone are presented for January and February 1979. The temporal and spatial averages and variability of ozone during this period are discussed. Retrieved total column ozone data derived from the MFR measurements for January 1979 are compared with preliminary SBUV measurements and with distributions of total ozone measured between 1958 and 1967.

Luther, F.M.; Ellis, J.S.; Lovill, J.E.; Sullivan, T.J.; Weichel, R.L.

1980-09-01T23:59:59.000Z

433

Algal Lipid Extraction and Upgrading to Hydrocarbons Technology Pathway  

Science Conference Proceedings (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

434

Biological Conversion of Sugars to Hydrocarbons Technology Pathway  

SciTech Connect

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

435

Plasma-induced conversion of surface-adsorbed hydrocarbons  

DOE Green Energy (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

436

Plasma-induced conversion of surface-adsorbed hydrocarbons  

DOE Green Energy (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

437

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

438

Aryl hydrocarbon mono-oxygenase activity in human lymphocytes  

SciTech Connect

Aryl hydrocarbon mono-oxygenase (AHM), an enzyme of key importance in metabolism of xenobiotic chemicals such as polynuclear aromatic hydrocarbons (PNA), is present in human lymphocytes. Studies investing the relation of activity of AHM in human lymphocytes to parameters such as disease state, PNA exposure, in vitro mitogen stimulation, etc. have been summarized in this report. Some studies have demonstrated increased AHM activity in lymphocytes from cigarette smokers (compared to nonsmokers), and in lung cancer patients when compared to appropriate control groups. These observations are confused by extreme variability in human lymphocyte AHM activities, such variability arising from factors such as genetic variation in AHM activity, variation in in vitro culture conditions which affect AHM activity, and the problematical relationship of common AHM assays to actual PNA metabolism taking place in lymphocytes. If some of the foregoing problems can be adequately addressed, lymphocyte AHM activity could hold the promise of being a useful biomarker system for human PNA exposure.

Griffin, G.D.; Schuresko, D.D.

1981-06-01T23:59:59.000Z

439

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 to 900{degrees}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 to 850{degrees}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, R.V.

1991-05-15T23:59:59.000Z

440

Environmental Distribution of Petroleum Hydrocarbons at a Utility Service Center  

Science Conference Proceedings (OSTI)

This report presents the results of a field study at a utility service center located in western New York where a petroleum product had leaked into the subsurface over a number of years. The study was a tailored collaboration effort between the Electric Power Research Institute (EPRI) and the Niagara Mohawk Power Corporation, aimed at delineating the nature and extent of migration of the dissolved hydrocarbons. The information is of interest to many utilities as they develop and implement management prac...

1999-06-30T23:59:59.000Z

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
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441

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

442

Determining Polycyclic Aromatic Hydrocarbon (PAH) Background in Sediments  

Science Conference Proceedings (OSTI)

Sediment remediation challenges at former manufactured gas plant (MGP) sites include defining sediment remedial zones, establishing risk-based remedial goals for specific polycyclic aromatic hydrocarbons (PAHs), and determining background conditions in what are often highly industrialized waterways. This technical update describes the various tools and approaches developed over approximately the past decade to determine site-specific background PAH concentrations in sediments attributable to ...

2012-11-14T23:59:59.000Z

443

Irregular spacing of heat sources for treating hydrocarbon containing formations  

SciTech Connect

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

444

Conversion of ethane and of propane to higher olefin hydrocarbons  

DOE Green Energy (OSTI)

It has become apparent during the past few months that results obtained in the oxidative coupling of methane cannot be extended to ethane and propane. Good selectivities and yields for the oxydehydrogenation to olefins can be obtained but production of higher hydrocarbons is small. The present report summarizes results of experiments using zeolite based catalysts and compares these with basic oxide catalysts. The oxydehydrogenation of ethane over zeolite based catalysts (H[sup [minus plus

Heinemann, H.; Somorjai, G.A.

1992-09-01T23:59:59.000Z

445

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

446

Aerobic microorganism for the degradation of chlorinated aliphatic hydrocarbons  

DOE Patents (OSTI)

This invention pertains to 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, C.B.

1988-10-12T23:59:59.000Z

447

Challenge for Mesozoic hydrocarbon exploration in the Eastern Indonesia  

Science Conference Proceedings (OSTI)

The eastern part of Indonesia covers approximately 3 million square kilometers, 35 percent being landmass and 65 percent covered by ocean. Only three of 38 sedimentary basins are producing hydrocarbon (Salawati, Bintuni, and Seram Basins). Oil and gas have discovered in the Lariang, Bone, Timor, Banggai, Sula and Biak Basins, however the discoveries have not developed yet. Hydrocarbon systems in Northern Australia and Papua New Guinea give the major contributions to the geological idea of Pre-Tertiary section in the less explored area in the Eastern Indonesia. The Triassic-Middle Jurassic marine carbonaceous shale sequences are the main hydrocarbon source rock in the Irian Jaya and surrounding area (Buton, gula and Seram basins). The main Mesozoic reservoir are the Kembelangan Formation in the Bintuni Basin of Irian Jaya and Bobong Formation in the North Sula Region. Exploration play types in the Eastern Indonesia can be divided into five types: 1 - Peri Cratonic, 2 - Marginal Rift Graben, 3 - Thrust Fold Belt Island Arc, 4 - Early Collision and 5 -Microcontinental Block - Advanced Collision. Recent discoveries through Mesozoic section in Eastern Indonesia are: Roabiba-1 (1990) in Bintuni Basin-Irian Jaya (Kambelangan Formation); Loku- 1 (1990) in North Sula region (Pre-Tertiary sediments); Oseil-1 (1993/94) in Bula-Seram Basin (Jurassic Manusela Formation); Elang-1 (1 994); Kakaktua-1 (1994) and Laminaria-1 in North Bonaparte Basin (Upper Jurassic Sands).

Abdullah, S.; Rukmiati, M.G.; Sitompul, N. (Pertamina Exploration and Production, Jakarta (Indonesia))

1996-01-01T23:59:59.000Z

448

Method for production of hydrocarbon diluent from heavy crude oil  

Science Conference Proceedings (OSTI)

This patent describes a method of producing a hydrocarbon diluent from a heavy crude oil extracted from an underground petroleum formation via a production well. It comprises: preheating a quantity of heavy crude oil extracted from the production well to yield a heated crude oil; separating in a separator vessel by flashing the heated crude oil to produce a first vapor fraction and a first liquid fraction; thermally cracking in a cracking unit at least a portion of the first liquid fraction to produce a first liquid effluent; quenching the first liquid effluent; introducing at least a portion of the quenched fist liquid effluent into a separator; condensing the first vapor fraction; separating in a separator vessel the condensed vapor fraction to produce a liquid hydrocarbon diluent middle fraction characterized in having a boiling range between about 400{degrees}-700{degrees}F. and a gas; and, directing the liquid hydrocarbon diluent into the formation via an injection well for enhancing production of petroleum from the formation via the production well.

McCants, M.F.

1992-05-05T23:59:59.000Z

449

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

450

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

451

Thermocatalytic CO2-Free Production of Hydrogen from Hydrocarbon Fuels  

DOE Green Energy (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

452

Conversion of Biomass-Derived Furans into Hydrocarbon Fuels  

Science Conference Proceedings (OSTI)

One of the most studied chemical transformations of carbohydrates is their thermocatalytic dehydration to form furans. Cellulose-derived glucose is thereby converted into 5-hydroxymethylfurfuraldehyde (5-HMF), while the hemicellulose-derived pentoses (e.g., xylose, arabinose) form furfuraldehyde. Our objective is to identify new pathways to convert furfuryl alcohol into a mixture of aliphatic hydrocarbons that can be used as drop-in fuels for diesel (C10-20) and jet fuel (C9-16) blends. Furfuryl alcohol is produced commercially through hydrogenation of furfuraldehyde that is derived from hemicellulose-derived pentoses via acid-catalyzed dehydration. The steps that we are currently pursuing to convert furfuryl alcohol into hydrocarbons are 1) oligomerization of furfuryl alcohol to form dimers (C10) and trimers (C15), and 2) hydrotreatment of the dimers and trimers to produce a mixture of linear hydrocarbons with carbon chain lengths in the range of diesel and jet fuels. This presentation will discuss our progress in the development of this pathway.

Moens, L.; Johnson, D. K.

2013-01-01T23:59:59.000Z

453

A Kalman-filter bias correction of ozone deterministic, ensemble-averaged, and probabilistic forecasts  

SciTech Connect

Kalman filtering (KF) is used to postprocess numerical-model output to estimate systematic errors in surface ozone forecasts. It is implemented with a recursive algorithm that updates its estimate of future ozone-concentration bias by using past forecasts and observations. KF performance is tested for three types of ozone forecasts: deterministic, ensemble-averaged, and probabilistic forecasts. Eight photochemical models were run for 56 days during summer 2004 over northeastern USA and southern Canada as part of the International Consortium for Atmospheric Research on Transport and Transformation New England Air Quality (AQ) Study. The raw and KF-corrected predictions are compared with ozone measurements from the Aerometric Information Retrieval Now data set, which includes roughly 360 surface stations. The completeness of the data set allowed a thorough sensitivity test of key KF parameters. It is found that the KF improves forecasts of ozone-concentration magnitude and the ability to predict rare events, both for deterministic and ensemble-averaged forecasts. It also improves the ability to predict the daily maximum ozone concentration, and reduces the time lag between the forecast and observed maxima. For this case study, KF considerably improves the predictive skill of probabilistic forecasts of ozone concentration greater than thresholds of 10 to 50 ppbv, but it degrades it for thresholds of 70 to 90 ppbv. Moreover, KF considerably reduces probabilistic forecast bias. The significance of KF postprocessing and ensemble-averaging is that they are both effective for real-time AQ forecasting. KF reduces systematic errors, whereas ensemble-averaging reduces random errors. When combined they produce the best overall forecast.

Monache, L D; Grell, G A; McKeen, S; Wilczak, J; Pagowski, M O; Peckham, S; Stull, R; McHenry, J; McQueen, J

2006-03-20T23:59:59.000Z

454

Modeling the Effect of Chlorine Emissions on Ozone Levels over the Eastern United States  

E-Print Network (OSTI)

This paper presents model estimates of the effect of chlorine emissions on atmospheric ozone concentrations in the eastern United States. The model included anthropogenic molecular chlorine emissions, anthropogenic hypochlorous acid emissions from cooling towers and swimming pools, and chlorine released from sea-salt aerosols. The release of chlorine emissions from sea-salt aerosols was modeled using heterogeneous reactions involving chloride ions in aerosols and three gas-phase species. The gas-phase chlorine chemistry was combined with the Carbon Bond Mechanism and incorporated into the Community Multiscale Air Quality modeling system. Air quality model simulations were performed for July 2001 and the results obtained with and without chlorine emissions were analyzed. When chlorine emissions were included in the model, ozone concentrations increased in the Houston, Texas, and New York–New Jersey areas. The daily maximum 1-h ozone concentrations increased by up to 12 parts per billion by volume (ppbv) in the Houston area and 6 ppbv in the New York–New Jersey area. The daily maximum 8-h ozone concentrations increased by up to 8 ppbv in the Houston area and 4 ppbv in the New York–New Jersey area. The monthly average daily maximum 1-h ozone concentration increased by up to 3 ppbv in the Houston area, but the increases in the monthly average daily maximum 1-h ozone concentration in the New York–New Jersey area were small. Chlorine emissions and chemistry enhanced the volatile organic compound oxidation rates and, thereby, increased the ozone production rate. 1.

Golam Sarwar; Prakash; V. Bhave

2006-01-01T23:59:59.000Z

455

Seismic Evaluation of Hydrocarbon Saturation in Deep-Water Reservoirs  

SciTech Connect

During this last period of the ''Seismic Evaluation of Hydrocarbon Saturation in Deep-Water Reservoirs'' project (Grant/Cooperative Agreement DE-FC26-02NT15342), we finalized integration of rock physics, well log analysis, seismic processing, and forward modeling techniques. Most of the last quarter was spent combining the results from the principal investigators and come to some final conclusions about the project. Also much of the effort was directed towards technology transfer through the Direct Hydrocarbon Indicators mini-symposium at UH and through publications. As a result we have: (1) Tested a new method to directly invert reservoir properties, water saturation, Sw, and porosity from seismic AVO attributes; (2) Constrained the seismic response based on fluid and rock property correlations; (3) Reprocessed seismic data from Ursa field; (4) Compared thin layer property distributions and averaging on AVO response; (5) Related pressures and sorting effects on porosity and their influence on DHI's; (6) Examined and compared gas saturation effects for deep and shallow reservoirs; (7) Performed forward modeling using geobodies from deepwater outcrops; (8) Documented velocities for deepwater sediments; (9) Continued incorporating outcrop descriptive models in seismic forward models; (10) Held an open DHI symposium to present the final results of the project; (11) Relations between Sw, porosity, and AVO attributes; (12) Models of Complex, Layered Reservoirs; and (14) Technology transfer Several factors can contribute to limit our ability to extract accurate hydrocarbon saturations in deep water environments. Rock and fluid properties are one factor, since, for example, hydrocarbon properties will be considerably different with great depths (high pressure) when compared to shallow properties. Significant over pressure, on the other hand will make the rocks behave as if they were shallower. In addition to the physical properties, the scale and tuning will alter our hydrocarbon indicators. Gas saturated reservoirs change reflection amplitudes significantly. The goal for the final project period was to systematically combine and document these various effects for use in deep water exploration and transfer this knowledge as clearly and effectively as possible.

Michael Batzle

2006-04-30T23:59:59.000Z

456

K. Toyota et al.: 3-D modeling of boundary-layer bromine and ozone in the Arctic (Supplement) 1 Supplement to "Analysis of reactive bromine production and ozone  

E-Print Network (OSTI)

K. Toyota et al.: 3-D modeling of boundary-layer bromine and ozone in the Arctic (Supplement) 1 3-D simulations with GEM-AQ: Inference from synoptic-scale patterns" K. Toyota1,2 , J. C. McConnell1. Toyota (kenjiro.toyota@ec.gc.ca) scale forcing resolved well at the grid resolution used in the present

Meskhidze, Nicholas

457

Incorporating TOMS Ozone Measurements into the Prediction of the Washington, D.C., Winter Storm during 24–25 January 2000  

Science Conference Proceedings (OSTI)

In this study, a methodology is proposed for incorporating total column ozone data from the Total Ozone Mapping Spectrometer (TOMS) into the initial conditions of a mesoscale prediction model. Based on the strong correlation between vertical mean ...

Kun-Il Jang; X. Zou; M. S. F. V. De Pondeca; M. Shapiro; C. Davis; A. Krueger

2003-06-01T23:59:59.000Z

458

Applications of the Regional Atmospheric Modeling System (RAMS) to Provide Input to Photochemical Grid Models for the Lake Michigan Ozone Study (LMOS)  

Science Conference Proceedings (OSTI)

In spite of ongoing control measures, episodes of elevated boundary layer ozone in violation of national ambient air quality standards continue to occur in the Lake Michigan region. The Lake Michigan Ozone Study is a multiyear effort that ...

Walter A. Lyons; Craig J. Tremback; Roger A. Pielke

1995-08-01T23:59:59.000Z

459

Observation-Based Assessment of the Impact of Nitrogen Oxides Emissions Reductions on Ozone Air Quality over the Eastern United States  

Science Conference Proceedings (OSTI)

Ozone is produced by chemical interactions involving nitrogen oxides (NOx) and volatile organic compounds in the presence of sunlight. At high concentrations, ground-level ozone has been shown to be harmful to human health and to the environment. ...

Edith Gégo; P. Steven Porter; Alice Gilliland; S. Trivikrama Rao

2007-07-01T23:59:59.000Z

460

Essays on the Impact of Climate Change and Building Codes on Energy Consumption and the Impact of Ozone on Crop Yield  

E-Print Network (OSTI)

15.2 Crop yield14 Impact of ozone on crop yield 15 Data 15.1 Ozonecrop . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

Aroonruengsawat, Anin

2010-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "monoxide ozone hydrocarbon" from the National Library of EnergyBeta (NLEBeta).
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461

EFFICIENCY OF OZONE PRODUCTION IN THE HOUSTON PLUME.  

SciTech Connect

Ozone levels observed during a field campaign in Houston were significantly higher than that observed in Phoenix or Philadelphia. An examination of the slope of O{sub x} versus NO{sub z} in the urban plumes shows that NO{sub x} is used 2 to 3 times more efficiently in Houston as compared with Phoenix and Philadelphia. Representative values of OPEx are 7-12, 3, and 4, in Houston, Phoenix, and Philadelphia. Aircraft observations have been used to calculate P(O{sub 3})/P(NO{sub z}). Values in Houston are significantly higher than in Phoenix and Philadelphia. We show that P(O{sub 3})/P(NO{sub z}) is proportional to a VOC/NO{sub 2}-OH reactivity ratio. High values of P(O{sub 3})/P(NO{sub z}) in Houston are due to emissions of reactive olefins from the ship channel region. It is significant that high values of P(O{sub 3})/P(NO{sub z}) occur at NO{sub x} levels up to several 10's of ppb. Not only is the chemistry efficient but it will be long lasting. The occurrence of high NO{sub x} and high OPEx is fostered by the co-location of VOC and NO{sub x} sources in the Houston industrial areas.

KLEINMAN,L.I.; DAUM,P.H.; BRECHTEL,F.; LEE,Y.N.; NUNNERMACKER,L.J.; SPRINGSTON,S.R.; WEINSTEIN-LLOYD,J.

2001-10-01T23:59:59.000Z

462

Application of dynamic linear regression to improve the skill of ensemble-based deterministic ozone forecasts  

SciTech Connect

Forecasts from seven air quality models and surface ozone data collected over the eastern USA and southern Canada during July and August 2004 provide a unique opportunity to assess benefits of ensemble-based ozone forecasting and devise methods to improve ozone forecasts. In this investigation, past forecasts from the ensemble of models and hourly surface ozone measurements at over 350 sites are used to issue deterministic 24-h forecasts using a method based on dynamic linear regression. Forecasts of hourly ozone concentrations as well as maximum daily 8-h and 1-h averaged concentrations are considered. It is shown that the forecasts issued with the application of this method have reduced bias and root mean square error and better overall performance scores than any of the ensemble members and the ensemble average. Performance of the method is similar to another method based on linear regression described previously by Pagowski et al., but unlike the latter, the current method does not require measurements from multiple monitors since it operates on individual time series. Improvement in the forecasts can be easily implemented and requires minimal computational cost.

Pagowski, M O; Grell, G A; Devenyi, D; Peckham, S E; McKeen, S A; Gong, W; Monache, L D; McHenry, J N; McQueen, J; Lee, P

2006-02-02T23:59:59.000Z

463

TSD- aa Trends in Measured 1-h Ozone Concentrations over the OTR  

E-Print Network (OSTI)

Trends in raw and meteorologically adjusted 1-hour ozone were calculated at several AQS monitoring sites in the Northeast. A summary of the analysis is provided below, and a detailed description of the met-adjustment procedure is outlined in Milanchus et al. (1998) and references contained including those related to the Kolmogorov-Zurbenko (KZ) method used in this analysis to estimate trends. Data Ozone time series were obtained at many monitoring sites in the Northeastern United States. From these data, log of daily maximum one hour ozone were calculated. In addition, several meteorological variables were obtained from National Weather service stations in the Northeast. These included surface temperature, dew point and specific humidity with dew point depression being calculated. Daily maximum values were calculated for each of the meteorological variable times series. The time span of data considered for both ozone and meteorological variables was from 1985 to 2005. In addition, this analysis focused on the ozone season (April 15 through October 15) of each year.

Modeling Domain

2007-01-01T23:59:59.000Z

464

Method for direct production of carbon disulfide and hydrogen from hydrocarbons and hydrogen sulfide feedstock  

DOE Patents (OSTI)

A method for converting hydrocarbons and hydrogen sulfide to carbon disulfide and hydrogen is provided comprising contacting the hydrocarbons and hydrogen sulfide to a bi-functional catalyst residing in a controlled atmosphere for a time and at a temperature sufficient to produce carbon disulfide and hydrogen. Also provided is a catalyst for converting carbon sulfides and hydrogen sulfides to gasoline range hydrocarbons comprising a mixture containing a zeolite catalyst and a hydrogenating catalyst.

Miao, Frank Q.; Erekson, Erek James

1998-12-01T23:59:59.000Z

465

Variational Assimilation of GOME Total-Column Ozone Satellite Data in a 2D Latitude–Longitude Tracer-Transport Model  

Science Conference Proceedings (OSTI)

A four-dimensional data-assimilation method is described to derive synoptic ozone fields from total-column ozone satellite measurements. The ozone columns are advected by a 2D tracer-transport model, using ECMWF wind fields at a single pressure ...

H. J. Eskes; A. J. M. Piters; P. F. Levelt; M. A. F. Allaart; H. M. Kelder

1999-10-01T23:59:59.000Z

466

Analysis of an Ozone Episode during the San Diego Air Quality Study: The Significance of Transport Aloft  

Science Conference Proceedings (OSTI)

San Diego is subject to transport of ozone and precursors from the Los Angeles area, 170 km to the northwest, as well as to high ozone concentrations from local emissions. The San Diego Air Quality Study was conducted during the summer of 1989. ...

Virginia Bigler-Engler; Hal W. Brown

1995-08-01T23:59:59.000Z

467

Repeatability of the Seasonal Variations of Ozone near the Mesopause from Observations of the 11.072-GHz Line  

Science Conference Proceedings (OSTI)

Ground-based observations of the 11.072-GHz line of ozone were made from January 2008 through the middle of September 2011 to estimate the maximum in the nighttime ozone in the upper mesosphere at an altitude of about 95 km for a region centered ...

A. E. E. Rogers; P. Erickson; V. L. Fish; J. Kittredge; S. Danford; J. M. Marr; M. B. Arndt; J. Sarabia; D. Costa; S. K. May

2012-10-01T23:59:59.000Z

468

Uncertainties in Predicted Ozone Concentrations Due to Input Uncertainties for the UAM-V Photochemical Grid Model  

Science Conference Proceedings (OSTI)

Based on studies of ozone episodes in the eastern United States using the photochemical grid model, UAM-V, regulatory agencies have made decisions concerning emissions controls. This project analyzes effects of uncertainties in UAM-V input variables (emissions, initial and boundary conditions, meteorological variables, and chemical reactions) on uncertainties in UAM-V ozone predictions for the July 1995 episode.

2000-11-06T23:59:59.000Z

469

Seasonal and Diurnal Variations of Ozone near the Mesopause from Observations of the 11.072-GHz Line  

Science Conference Proceedings (OSTI)

Ground-based observations of the 11.072-GHz line of ozone were made from January 2008 through January 2009. These observations provide an estimate of the diurnal and seasonal variations of ozone in the mesopause region. The 11-GHz line is more ...

A. E. E. Rogers; M. Lekberg; P. Pratap

2009-10-01T23:59:59.000Z

470

Effect of temperature on wave velocities in sands and sandstones with heavy hydrocarbons  

SciTech Connect

A laboratory investigation was made of the effects of temperature on wave velocities in well cemented Massillon and Boise sandstones and unconsolidated Ottawa sand saturated with heavy hydrocarbons, as well as the dependence of compressional velocities in the hydrocarbons themselves as a function of temperature. The hydrocarbons selected as pore saturants were a commercial paraffin wax, 1-Eicosene, natural heavy crude, and natural tar. The experimental results show that the compressional wave velocities in the hydrocarbons decrease markedly with increasing temperature. In contrast wave velocities in the Massillon and Boise sandstones and unconsolidated Ottawa sand saturated with air or water decrease only little with increasing temperatures. The main reason for the large decreases in rocks with hydrocarbons is the melting of solid hydrocarbons, and high pore pressure. Thermal expansion of the saturants, and possibly thermal cracking of the heavy fractions and vaporization of the light fractions of the hydrocarbons may also contribute. The large decreases of the compressional and shear wave velocities in the hydrocarbon-saturated rocks and sands with temperature, suggest that seismic measurements such as used in seismology or borehole tomography may be very useful in detecting steam fronts in heavy hydrocarbon reservoirs undergoing steam flooding.

Wang, Z.; Nur, A.M.

1986-01-01T23:59:59.000Z

471

Catalytic conversion of C3+ alcohols to hydrocarbon blend-stock  

Catalytic conversion of C3+ alcohols to hydrocarbon blend-stock Note: The technology described above is an early stage opportunity. Licensing rights to this ...

472

Rare earth elements (REE) as geochemical clues to reconstruct hydrocarbon generation history.  

E-Print Network (OSTI)

??The REE distribution patterns and total concentrations of the organic matter of the Woodford shale reveal a potential avenue to investigate hydrocarbon maturation processes in… (more)

Ramirez-Caro, Daniel

2013-01-01T23:59:59.000Z

473

Hydrocarbon solubility and its migration processes: a look at the present status  

DOE Green Energy (OSTI)

In this study we review the present status of knowledge of solubility of hydrocarbons and its implications on primary migration processes. The intent is to examine the solubility and the transportation mechanisms relevant to geopressured-geothermal reservoirs, although the discussion included here accommodates a wide range of related aspects. Influences of parameters associated with hydrocarbon (especially methane) solubility have been studied. We have sought to evaluate several primary hydrocarbon migration processes and to point out their attractive features as well as their limitations. A brief discussion of hydrocarbon generation processes is also included.

Mamun, C.K.; Ohkuma, H.; Sepehrnoori, K.

1985-12-01T23:59:59.000Z

474

Optical constants of evaporation-deposited silicon monoxide films in the 7.1–800 eV photon energy range  

Science Conference Proceedings (OSTI)

The transmittance of silicon monoxide films prepared by thermal evaporation was measured from 7.1 to 800 eV and used to determine the optical constants of the material. SiO filmsdeposited onto C-coated microgrids in ultrahigh vacuum conditions were measured in situ from 7.1 to 23.1 eV. Grid-supported SiO filmsdeposited in high vacuum conditions were characterized ex situ from 28.5 to 800 eV. At each photon energy

Mónica Fernández-Perea; Manuela Vidal-Dasilva; Juan I. Larruquert; José A. Aznárez; José A. Méndez; Eric Gullikson; Andy Aquila; Regina Soufli

2009-01-01T23:59:59.000Z

475

The Reaction Specificity of Nanoparticles in Solution: Application to the Reaction of Nanoparticulate Iron and Iron-Bimetallic Compounds with Chlorinated Hydrocarbons and Oxyanions  

SciTech Connect

The prospect for better remediation technologies using nanoparticles of iron, iron oxides, and iron with catalytic metals (i.e., bimetallics) has potentially transformative implications for environmental management of DOE sites across the country. Of particular interest is the potential to avoid undesirable products from the degradation of chlorinated solvents by taking advantage of the potential selectivity of nanoparticles to produce environmentally benign products from CCl{sub 4}. Chlorinated solvents are the most frequently reported subsurface contaminants across the whole DOE complex, and carbon tetrachloride (CCl{sub 4}) is the chlorinated solvent that is of greatest concern at Hanford (U. S. Department Energy 2001). In evaluating technologies that might be used at the site, a critical concern will be that CCl{sub 4} reduction usually occurs predominantly by hydrogenolysis to chloroform (CHCl{sub 3}) and methylene chloride (CH{sub 2}Cl{sub 2}), both of which are nearly as problematic as CCl{sub 4} (National Research Council, 1978). Competing reaction pathways produce the more desirable products carbon monoxide (CO) and/or formate (HCOO{sup -}), and possibly CO{sub 2}, but the proportion of reaction that occurs by these pathways is highly variable. Iron-based metallic and oxide nanoparticles have been shown to have enhanced reactivity towards a variety of chemical species, including chlorinated hydrocarbons and reducible oxyanions. Possibly of greater importance is the ability of nanoparticles to select for specific reaction products, potentially facilitating the formation of more environmentally acceptable products. The purpose of this study is to develop a fundamental understanding of the mechanism responsible for the overall particle reactivity and reaction selectivity of reactive metal and oxide nanoparticles. To achieve this objective the project involves the synthesis (using solution and vacuum synthesis methods) and characterization of well-defined nanoparticles, measurements of particle reactivity in solution or vacuum environments, and theory and modeling efforts to rationalize particle structure and reactivity.

None

2005-06-01T23:59:59.000Z

476

Two decades of hydrocarbon exploration activity in Indonesia  

SciTech Connect

During the past two decades, hydrocarbon exploration activity within Indonesia has been based on the Indonesian Energy Policy, aims of which include intensifying and expanding hydrocarbon exploration programs. Expansion into the offshore regions of the nation has resulted in the discovery of petroliferous basins. The first offshore oil production came on stream in 1971. Since then, significant achievements have been made in developing these resources. Intensified onshore exploration has resulted in additional oil fields being discovered in these more mature areas. Among the significant gas fields discovered during the past 20 years, Arun and Badak both supply major LNG projects. Oil fields have been found in the onshore areas of Sumatra, Kalimantan, Java, and Irian Jaya, and in the offshore areas around West Java, Madura, Natuna, and East Kalimantan. The exploration drilling success during this time has been approximately 32%. In addition, the ratio of oil field development to these discoveries is about 54%. For technical and economic reasons, not all discoveries can be developed into oil fields. Recently, Pertamina's Research and Development Division organized the study of data contributed by Pertamina exploration, foreign contractors, and science institutes. This study reveals that 60 basins are spread throughout the onshore and offshore areas of the nation. Using PAUS (plan and analysis of uncertainty situation), a Monte Carolo simulation program, the hydrocarbon potential of each basin has been estimated. These estimates will be continually revised as more data are made available to the study, as the geology of Indonesia is better understood in terms of plate tectonic theory, and as computing techniques improve.

Suardy, A.; Taruno, J.; Simbolon, P.H.; Simbolon, B.

1986-07-01T23:59:59.000Z

477

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

Science Conference Proceedings (OSTI)

We used Proton Transfer Reaction - Mass Spectrometry (PTR-MS) and conventional sampling methods to monitor and identify trace level organic pollutants formed in heterogeneous reactions between ozone and HVAC filters in real time. Experiments were carried out using a bench-scale flow tube reactor operating with dry air and humidified air (50% RH), at realistically high ozone concentrations (150 ppbv). We explored different filter media (i.e., fiberglass and cotton/polyester blends) and different particle loadings (i.e., clean filter and filters loaded with particles for 3 months at the Lawrence Berkeley National Laboratory and the Port of Oakland, CA). Detailed emission dynamics of very low levels of certain organic pollutants from filter media upon ozone exposure in the presence of moisture have been obtained and analyzed.

Destaillats, Hugo; Chen, Wenhao; Apte, Michael; Li, Nuan; Spears, Michael; Almosni, Jérémie; Zhang, Jianshun (Jensen); Fisk, William J.

2009-09-09T23:59:59.000Z

478

Novel metalloporphyrin catalysts for the oxidation of hydrocarbons  

DOE Green Energy (OSTI)

Work was done for developing biomimetic oxidation catalysts. Two classes of metalloporphyrin catalysts were studied. The first class of catalysts studied were a novel series of highly substituted metalloporphyrins, the fluorinated iron dodecaphenylporphyrins. These homogeneous metalloporphyrin catalysts were screened for activity as catalysts in the oxidation of hydrocarbons by dioxygen. Results are discussed with respect to catalyst structural features. The second type of catalysts studied were heterogeneous catalysts consisting of metalloporphyrins applied to inorganic supports. Preliminary catalytic testing results with these materials are presented.

Showalter, M.C.; Nenoff, T.M.; Shelnutt, J.A.

1996-11-01T23:59:59.000Z

479

Direct conversion of light hydrocarbon gases to liquid fuel  

DOE Green Energy (OSTI)

The objective of this program is to investigate the direct conversion of light gaseous hydrocarbons, such as those produced during Fischer-Tropsch synthesis or as a product of gasification, to liquid transportation fuels via a partial oxidation process. The process will be tested in an existing pilot plant to obtain credible mass balances. Specific objectives to be met include determination of optimal process conditions, investigation of various processing options (e.g. feed injection, product quench, and recycle systems), and evaluation of an enhanced yield thermal/catalytic system. Economic evaluation of the various options will be performed as experimental data become available.

Foral, M.J.

1991-01-01T23:59:59.000Z

480

Direct conversion of light hydrocarbon gases to liquid fuel  

DOE Green Energy (OSTI)

The objective of this program is to investigate the direct conversion of light gaseous hydrocarbons, such as those produced during Fischer-Tropsch synthesis or as a product of gasification, to liquid transportation fuels via a partial oxidation process. The process will be tested in an existing pilot plant to obtain credible mass balances. Specific objectives to be met include determination of optimal process conditions, investigation of var