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


1

Methane, Nonmethane Hydrocarbons, Alkyl Nitrates, and Chlorinated Carbon  

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

Atmospheric Trace Gases in Whole-Air Samples Atmospheric Trace Gases in Whole-Air Samples Methane, Nonmethane Hydrocarbons, Alkyl Nitrates, and Chlorinated Carbon Compounds including 3 Chlorofluorocarbons (CFC-11, CFC-12, and CFC-113) in Whole-air Samples graphics Graphics data Data Investigator Donald Blake Department of Chemistry, University of California Irvine, California, 92697 USA Period of Record April 1979 - December 2012 Methods Whole-air samples are collected in conditioned, evacuated, 2-L stainless steel canisters; each canister is filled to ambient pressure over a period of about 1 minute (approximately 20 seconds to 2 minutes). These canisters are returned to the University of California at Irvine for chromatographic analysis. Analysis for methane includes gas chromatography with flame ionization, as

2

Gas/particle partitioning of total alkyl nitrates observed with TD-LIF in Bakersfield  

E-Print Network (OSTI)

total AN (gas + aerosol) and ANaer show that on average 21% of ANs are in the condensed phaseGas/particle partitioning of total alkyl nitrates observed with TD-LIF in Bakersfield A. W. Rollins samples. These measurements show that ANs are a ubiquitous component of the OA with the ­ONO2 subunit

Cohen, Ronald C.

3

Alkyl nitrate (C1-C3) depth profiles in the tropical Pacific Ocean E. E. Dahl,1,2  

E-Print Network (OSTI)

and distribution of tropo- spheric ozone. Atmospheric alkyl nitrates are normally associated with polluted air free radical processes initiated by radioactive decay or cosmic rays, enzymatically mediated reactions expedition in the equatorial Pacific, an equatorial maximum in atmospheric ethyl and isopropyl nitrate

Saltzman, Eric

4

Alkylate  

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

Day) Day) Product: Alkylate Aromatics Asphalt & Road Oil Isomers Isobutane Isopentane & Isohexane Isooctane Lubricants Marketable Petroleum Coke Hydrogen Sulfur Period: Annual (as of January 1) Download Series History Download Series History Definitions, Sources & Notes Definitions, Sources & Notes Show Data By: Product Area 2008 2009 2010 2011 2012 2013 View History U.S. 1,260,985 1,260,923 1,248,514 1,262,443 1,246,875 1,269,361 1982-2013 PAD District 1 110,229 110,229 95,500 108,629 79,429 91,429 1982-2013 Delaware 11,729 11,729 0 11,729 11,729 11,729 1982-2013 Florida 0 0 0 0 0 0 2007-2013 Georgia 0 0 0 0 0 0 2006-2013 Maryland 0 0 0 0 0 0 2007-2013 New Jersey 40,200 40,200 36,200 37,200 37,200 37,200 1982-2013

5

Transition metal ion-assisted photochemical generation of alkyl halides and hydrocarbons from carboxylic acids  

SciTech Connect

Near-UV photolysis of aqueous solutions of propionic acid and aqueous Fe3+ in the absence of oxygen generates a mixture of hydrocarbons (ethane, ethylene and butane), carbon dioxide, and Fe2+. The reaction becomes mildly catalytic (about five turnovers) in the presence of oxygen which converts a portion of alkyl radicals to oxidizing intermediates that reoxidize Fe2+. The photochemistry in the presence of halide ions (X? = Cl?, Br?) generates ethyl halides via halogen atom abstraction from FeXn3?n by ethyl radicals. Near-quantitative yields of C2H5X are obtained at ?0.05 M X?. Competition experiments with Co(NH3)5Br2+ provided kinetic data for the reaction of ethyl radicals with FeCl2+ (k = (4.0 ± 0.5) × 106 M?1 s?1) and with FeBr2+ (k = (3.0 ± 0.5) × 107 M?1 s?1). Photochemical decarboxylation of propionic acid in the presence of Cu2+ generates ethylene and Cu+. Longer-chain acids also yield alpha olefins as exclusive products. These reactions become catalytic under constant purge with oxygen which plays a dual role. It reoxidizes Cu+ to Cu2+, and removes gaseous olefins to prevent accumulation of Cu+(olefin) complexes and depletion of Cu2+. The results underscore the profound effect that the choice of metal ions, the medium, and reaction conditions exert on the photochemistry of carboxylic acids.

Carraher, Jack; Pestovsky, Oleg; Bakac, Andreja

2012-03-14T23:59:59.000Z

6

Alkyl nitrate (C 1 -C 3 ) depth profiles in the tropical Pacific Ocean  

E-Print Network (OSTI)

concentrations with a [ iPr]/[Et] ratio of 0.1±0.0. Noat all depths with an [iPr]/[Et] ratio of 0.2 ± 0.0. Thiswith ethyl nitrate with an [iPr]/[Et] ratio of 0.2 ± 0.0.

Dahl, E. E; Yvon-Lewis, S. A; Saltzman, E. S

2007-01-01T23:59:59.000Z

7

Preparation and use of tetra-alkyl cobalt dicarbollide for extraction of cesium and strontium into hydrocarbon solvents  

DOE Patents (OSTI)

Preparation and use of tetra-C-alkyl cobalt dicarbollide for extraction of cesium and strontium into hydrocarbon solvents. Tetra-C-alkyl derivatives of cobalt dicarbollide, Co(C.sub.2 R.sub.2 B.sub.9 H.sub.9).sub.2.sup.- (CoB.sub.2 R.sub.4.sup.- ; R=CH.sub.3 and C.sub.6 H.sub.13) are demonstrated to be significant cesium and strontium extractants from acidic and alkaline solutions into non-toxic organic solvent systems. Extractions using mesitylene and diethylbenzene are compared to those with nitrobenzene as the organic phase. CoB.sub.2 -hexyl.sub.4.sup.- in diethylbenzene shows improved selectivity (10.sup.4) for Cs over Na in acidic solution. In dilute alkaline solution, CoB.sub.2 -hexyl.sub.4.sup.- extracts Cs less efficiently, but more effectively removes Sr from higher base concentrations. A general synthesis of tetra-C-alkyl cobalt dicarbollides is described.

Miller, Rebecca L. (Los Alamos, NM); Pinkerton, Anthony B. (Santa Fe, NM); Abney, Kent D. (Los Alamos, NM); Kinkead, Scott A. (Los Alamos, NM)

1997-01-01T23:59:59.000Z

8

Process for using alkyl substituted C8-C10 aromatic hydrocarbons as preferential physical solvents for selective processing of hydrocarbon gas streams  

SciTech Connect

This patent describes a process for the removal of hydrocarbon gas liquids, comprising hydrocarbons heavier than methane, from a hydrocarbon gas stream. The improvement consists of selectively extracting the hydrocarbon gas liquids from the hydrocarbon gas stream with a preferential physical solvent which provides selective capability for recovery according to the selected degree of (a) ethane in amounts ranging from 2-98%, (b) propane in amounts ranging from 2-99%, (c) butane in amounts ranging from 2-100%, or (d) pentanes and higher molecular weight hydrocarbons in amounts ranging up to 100% which comprises: A. selectively extracting and stripping the hydrocarbon gas stream with the physical solvent to produce a residue hydrocarbon gas stream of pipeline specifications and a rich solvent stream containing ethane and heavier hydrocarbon components, the preferential physical solvent being: (1) rich in C/sub 8/-C/sub 10/ aromatic compounds having methyl, ethyl, or propyl aliphatic groups and (2) selective for ethane and heavier hydrocarbon components of the gas stream such that: (a) the relative volatility of methane over ethane is at least 5.0 and the hydrocarbon loading capacity, defined as solubility of ethane in solvent, is at least 0.25 standard cubic feet of ethane per gallon of solvent, or (b) the preferential factor determined by the multiplication of relative volatility of methane over ethane by the solubility of ethane in solvent, in standard cubic feet of ethane per gallon of solvent, of at least 1.25; and B. distilling the rich solvent to produce the hydrocarbon gas liquids and the physical solvent.

Mehra, Y.R.

1987-09-08T23:59:59.000Z

9

Nitrated and oxygenated derivatives of polycyclic aromatic hydrocarbons in the ambient air of two  

E-Print Network (OSTI)

polycyclic aromatic hydrocarbons; Size distribution; Atmospheric pollution; POVA (POllution des Vallées, published in "Atmospheric Environment 42, 173 (2008) 55 à 64" DOI : 10.1016/j.atmosenv.2007.10.008 #12 was determined during the intensive sampling campaigns of the POVA (POllution des Vallées Alpines) research

Boyer, Edmond

10

Adsorption of alkyl amides: monolayer structures and mixing behaviour  

E-Print Network (OSTI)

adsorbs hydrocarbons from liquid media [42-44]. Groszek [42] provided an explanation for the high affinity of the graphite surface for the hydrocarbons. The zigzag structure of the hydrocarbon fits well into the graphite hexagons (Figure 1... of the composition range. 1.3 Alkyl amides In this section the properties and applications of alkyl amides are explained, and a review of the adsorption of amides on different surfaces such as graphite, polymer surfaces and water is provided. The bulk...

Bhinde, Tej

2011-02-08T23:59:59.000Z

11

Degradation of Polycyclic Aromatic Hydrocarbons at Low Temperature under Aerobic and Nitrate-Reducing Conditions in Enrichment Cultures from Northern Soils  

Science Journals Connector (OSTI)

...from well-drained areas. In general, most successful enrichment...temperature and freeze-thaw cycles on hydrocarbon biodegradation...Krieg. 1994. Methods for general and molecular bacteriology...Canada creosote degradation diesel fuel Eastern Canada Ellesmere...

Mikael Eriksson; Erik Sodersten; Zhongtang Yu; Gunnel Dalhammar; William W. Mohn

2003-01-01T23:59:59.000Z

12

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

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

Environmental Sciences and Ecology 30 0600Fg--Chem--Forensic Oil Sampling 01 2010 ****DATA SOURCE**** Summary: M - Alkylated PAHs) Volatile Organic Hydrocarbons -- Paraffins,...

13

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

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

Environmental Sciences and Ecology 30 0600Fg--Chem--Forensic Oil Sampling 01 2010 ****DATA SOURCE**** Summary: M - Alkylated PAHs) Volatile Organic Hydrocarbons -- Paraffins,...

14

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

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

Environmental Sciences and Ecology 30 0600Fg--Chem--Forensic Oil Sampling 01 2010 ****DATA SOURCE**** Summary: M - Alkylated PAHs) Volatile Organic Hydrocarbons -- Paraffins,...

15

Nitrate reduction  

DOE Patents (OSTI)

Nitrates are reduced to nitrogen gas by contacting the nitrates with a metal to reduce the nitrates to nitrites which are then contacted with an amide to produce nitrogen and carbon dioxide or acid anions which can be released to the atmosphere. Minor amounts of metal catalysts can be useful in the reduction of the nitrates to nitrites. Metal salts which are formed can be treated electrochemically to recover the metals.

Dziewinski, Jacek J. (Los Alamos, NM); Marczak, Stanislaw (Los Alamos, NM)

2000-01-01T23:59:59.000Z

16

Alkylating Properties of Phosphoramide Mustard  

Science Journals Connector (OSTI)

...undergoes alkylation reactions as an intact molecule...rather than a direct SN2 displacement of the chlorine...undergoes alkylation reactions as an intact molecule...ylamine formed in the reaction of phosphoramide mustard...alkylation by direct (SN2) displacement of the...

Michael Colvin; Robert B. Brundrett; Man-Na N. Kan; Ian Jardine; and Catherine Fenselau

1976-03-01T23:59:59.000Z

17

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

18

Method of making alkyl esters  

DOE Patents (OSTI)

Methods of making alkyl esters are described herein. The methods are capable of using raw, unprocessed, low-cost feedstocks and waste grease. Generally, the method involves converting a glyceride source to a fatty acid composition and esterifying the fatty acid composition to make alkyl esters. In an embodiment, a method of making alkyl esters comprises providing a glyceride source. The method further comprises converting the glyceride source to a fatty acid composition comprising free fatty acids and less than about 1% glyceride by mass. Moreover, the method comprises esterifying the fatty acid composition in the presence of a solid acid catalyst at a temperature ranging firm about 70.degree. C. to about 120.degree. C. to produce alkyl esters, such that at least 85% of the free fatty acids are converted to alkyl esters. The method also incorporates the use of packed bed reactors for glyceride conversion and/or fatty acid esterification to make alkyl esters.

Elliott, Brian (Wheat Ridge, CO)

2010-09-14T23:59:59.000Z

19

Hydrocarbon composition of crude oils near the Caspian depression  

SciTech Connect

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

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

1983-01-01T23:59:59.000Z

20

Production of methyl tert-alkyl ethers  

SciTech Connect

The transition to the use of unleaded gasolines has required the replacement of tetraethyl lead by oxygen-containing compounds such as methanol, ethanol, and ethers, which are termed {open_quotes}oxygenates{close_quotes} in the technical literature. These may be used in commercial gasolines in amounts of 10-15% by volume, equivalent to 2% oxygen by weight. When methyl tert-butyl ether (MTBE) is used, the oxygen content may amount to 2.7% by weight. This oxygenate gives a significant improvement of knock resistance of naphtha fractions, the greatest effects being observed for straight-run naphthas and reformer naphthas produced under normal conditions; the MTBE also improves the engine power and economy characteristics and lowers the carbon monoxide content in the exhaust by 15-30% and the hydrocarbon content by 7-8%. This paper describes methods for the production of MTBE and also methyl tert-alkyl ethers.

Trofimov, V.A.

1995-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "hydrocarbons alkyl nitrates" 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

Chemical nature of high-molecular hydrocarbons of gaseous condensates  

SciTech Connect

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

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

1987-01-01T23:59:59.000Z

22

Polyethylene composites containing a phase change material having a C14 straight chain hydrocarbon  

DOE Patents (OSTI)

A composite useful in thermal energy storage, said composite being formed of a polyethylene matrix having a straight chain alkyl hydrocarbon incorporated therein, said polyethylene being crosslinked to such a degree that said polyethylene matrix is form stable and said polyethylene matrix is capable of absorbing at least 10% by weight of said straight chain alkyl hydrocarbon; the composite is useful in forming pellets or sheets having thermal energy storage characteristics.

Salyer, Ival O. (Dayton, OH)

1987-01-01T23:59:59.000Z

23

Removal of trace olefins from aromatic hydrocarbons  

SciTech Connect

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

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

1989-01-03T23:59:59.000Z

24

Mild Catalytic methods for Alkyl-Alkyl Bond Formation  

SciTech Connect

Overview of Research Goals and Accomplishments for the Period 07/01/06 – 06/30/07: Our overall research goal is to transform the rapidly emerging synthetic chemistry involving alkyl-alkyl cross-couplings into more of a mechanism-based field so that that new, rationally-designed catalysts can be performed under energy efficient conditions. Our specific objectives for the previous year were 1) to obtain a proper electronic description of an active catalyst for alkyl-alkyl cross-coupling reactions and 2) to determine the effect of ligand structure on the rate, scope, selectivity, and functional group compatibility of C(sp3)-C(sp3) cross-coupling catalysis. We have completed both of these initial objectives and established a firm base for further studies. The specific significant achievements of the current grant period include: 1) we have performed magnetic and computational studies on (terpyridine)NiMe, an active catalyst for alkyl-alkyl cross couplings, and have discovered that the unpaired electron resides heavily on the terpyridine ligand and that the proper electronic description of this nickel complex is a Ni(II)-methyl cation bound to a reduced terpyridine ligand; 2) we have for the first time shown that alkyl halide reduction by terpyridyl nickel catalysts is substantially ligand based; 3) we have shown by isotopic labeling studies that the active catalyst (terpyridine)NiMe is not produced via a mechanism that involves the formation of methyl radicals when (TMEDA)NiMe2 is used as the catalyst precursor; 4) we have performed an extensive ligand survey for the alkyl-alkyl cross-coupling reactions and have found that electronic factors only moderately influence reactivity in the terpyridine-based catalysis and that the most dramatic effects arise from steric and solubility factors; 5) we have found that the use of bis(dialkylphosphino)methanes as ligands for nickel does not produce active catalysts for cross-coupling but rather leads to bridging hydride complexes of varying geometries; 6) we have determined that the geometry of aforementioned bridging hydride complexes is largely determined by external forces such as hydrogen bonding interactions and crystal packing forces; 7) we have found that the rate of reductive elimination of alkane from a (pyridyl-2-pyrrolide)AuMe2 complex is severely inhibited due to the rigid geometry of the pyridyl-2-pyrrolide ligand; 8) we have prepared, structurally characterized, and explored the reactivity of 1-adamantylzinc reagents as model nucleophiles for sterically challenging alkyl-alkyl cross-coupling reactions. The continued success of this work will lead to alkyl-alkyl cross-coupling catalysts with broad scope and selectivities. The work has potential to significantly impact science and technologies of interest to the DOE as the chemistry is focused on developing useful reactions using reagents that can be directly prepared from petroleum and natural gas feedstocks. Moreover, the developing synthetic chemistry can profoundly affect the way materials, fine chemicals, and drugs are made. Since the methodology we are developing can shorten existing synthetic protocols, proceed at room temperature, and operate under environmentally benign conditions, it can greatly reduce energy expenditures, especially considering the contribution of the chemical manufacturing field to the gross domestic product.

David A Vicic

2009-08-10T23:59:59.000Z

25

Thermochemical nitrate destruction  

DOE Patents (OSTI)

A method is disclosed for denitrification of nitrates and nitrates present in aqueous waste streams. The method comprises the steps of (1) identifying the concentration nitrates and nitrites present in a waste stream, (2) causing formate to be present in the waste stream, (3) heating the mixture to a predetermined reaction temperature from about 200.degree. C. to about 600.degree. C., and (4) holding the mixture and accumulating products at heated and pressurized conditions for a residence time, thereby resulting in nitrogen and carbon dioxide gas, and hydroxides, and reducing the level of nitrates and nitrites to below drinking water standards.

Cox, John L. (Richland, WA); Hallen, Richard T. (Richland, WA); Lilga, Michael A. (Richland, WA)

1992-01-01T23:59:59.000Z

26

The Mechanism of Action of Alkylating Agents  

Science Journals Connector (OSTI)

...the Sn2 and Sn1 reactors with their known...alkylating agents on nuclear material and cell...the Sn@ and Sni reactors with their known...alkylating agents on nuclear material and cell...then there was de generation, whereas with x-rays...oegiants, although nuclear granulation similar...

G. P. Warwick

1963-09-01T23:59:59.000Z

27

Thermochemical nitrate destruction  

DOE Patents (OSTI)

A method is disclosed for denitrification of nitrates and nitrites present in aqueous waste streams. The method comprises the steps of (1) identifying the concentration nitrates and nitrites present in a waste stream, (2) causing formate to be present in the waste stream, (3) heating the mixture to a predetermined reaction temperature from about 200 C to about 600 C, and (4) holding the mixture and accumulating products at heated and pressurized conditions for a residence time, thereby resulting in nitrogen and carbon dioxide gas, and hydroxides, and reducing the level of nitrates and nitrites to below drinking water standards.

Cox, J.L.; Hallen, R.T.; Lilga, M.A.

1992-06-02T23:59:59.000Z

28

Naphthenic hydrocarbons  

SciTech Connect

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

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

1987-01-01T23:59:59.000Z

29

Alkylation of organic aromatic compounds  

DOE Patents (OSTI)

Aromatic compounds are alkylated in a combination reactor/distillation column comprising a vessel suitable for operating between 70 C and 500 C and from 0.5 to 20 atmospheres pressure; an inert distillation packing in the lower one-third of said vessel; solid acidic catalytic material such as zeolites or an acidic cation exchange resin supported in the middle one-third of said vessel; and inert distillation packing in the upper one-third of said vessel. A benzene inlet is located near the upper end of the vessel; an olefin inlet is juxtaposed with said solid acidic catalytic material; a bottoms outlet is positioned near the bottom of said vessel for removing said cumene and ethyl benzene; and an overhead outlet is placed at the top of said vessel for removing any unreacted benzene and olefin.

Smith, L.A. Jr.; Arganbright, R.P.; Hearn, D.

1993-01-05T23:59:59.000Z

30

Alkylation of organic aromatic compounds  

DOE Patents (OSTI)

Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C[sub 2] to C[sub 10] olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80 C to 500 C, using as the catalyst a mole sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene below the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms. 1 fig.

Smith, L.A. Jr.

1989-07-18T23:59:59.000Z

31

Alkylation of organic aromatic compounds  

DOE Patents (OSTI)

Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C.sub.2 to C.sub.10 olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80.degree. C. to 500.degree. C., using as the catalyst a mole sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene below the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms.

Smith, Jr., Lawrence A. (Houston, TX)

1989-01-01T23:59:59.000Z

32

Alkylation of organic aromatic compounds  

DOE Patents (OSTI)

Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C.sub.2 to C.sub.10 olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80.degree. C. to 500.degree. C., using as the catalyst a mole sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene below the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms.

Smith, Jr., Lawrence A. (Bellaire, TX); Arganbright, Robert P. (Seabrook, TX); Hearn, Dennis (Houston, TX)

1994-01-01T23:59:59.000Z

33

Alkylation of organic aromatic compounds  

DOE Patents (OSTI)

Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C[sub 2] to C[sub 10] olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80 C to 500 C, using as the catalyst a molecular sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene to about the mid point of the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms. 1 figures.

Smith, L.A. Jr.; Arganbright, R.P.; Hearn, D.

1993-09-07T23:59:59.000Z

34

Alkylation of organic aromatic compounds  

DOE Patents (OSTI)

Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C[sub 2] to C[sub 10] olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80 C to 500 C, using as the catalyst a molecular sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene below the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms. 1 fig.

Smith, L.A. Jr.; Arganbright, R.P.; Hearn, D.

1994-06-14T23:59:59.000Z

35

Alkylation of organic aromatic compounds  

DOE Patents (OSTI)

Aromatic compounds are alkylated in a catalytic distillation, wherein the catalyst structure also serves as a distillation component by contacting the aromatic compound with a C.sub.2 to C.sub.10 olefin in the catalyst bed under 0.25 to 50 atmospheres of pressure and at temperatures in the range of 80.degree. C. to 500.degree. C., using as the catalyst a mole sieve characterized as acidic or an acidic cation exchange resin. For example, ethyl benzene is produced by feeding ethylene to about the mid point of the catalyst bed while benzene is conveniently added through the reflux in molar excess to that required to react with ethylene, thereby reacting substantially all of the ethylene and recovering benzene as the principal overhead and ethyl benzene in the bottoms.

Smith, Jr., Lawrence A. (Bellaire, TX); Arganbright, Robert P. (Seabrook, TX); Hearn, Dennis (Houston, TX)

1993-01-01T23:59:59.000Z

36

Wet Chemical Functionalization of III–V Semiconductor Surfaces: Alkylation of Gallium Arsenide and Gallium Nitride by a Grignard Reaction Sequence  

Science Journals Connector (OSTI)

Wet Chemical Functionalization of III–V Semiconductor Surfaces: Alkylation of Gallium Arsenide and Gallium Nitride by a Grignard Reaction Sequence ... These observations are consistent with the known solubility of oxidized As species in water. ... Remote H plasma exposure was effective for removing halogens and hydrocarbons from the surfaces of both nitrides at 450 °C, but was not efficient for oxide removal. ...

Sabrina L. Peczonczyk; Jhindan Mukherjee; Azhar I. Carim; Stephen Maldonado

2012-02-28T23:59:59.000Z

37

Present and Future Alkylation Processes in Refineries  

Science Journals Connector (OSTI)

Present and Future Alkylation Processes in Refineries ... Second, an accident at a Texas refinery released considerable amounts of gaseous HF. ... In addition, following an accident, it is uncertain whether the sprays would still be operable. ...

Lyle F. Albright

2009-01-08T23:59:59.000Z

38

GC/FTIR Study of Nitrated Polycyclic Aromatic Hydrocarbons  

Science Journals Connector (OSTI)

......addressed. Department of Chemistry, Mississippi State...Whitehead Department of Chemistry, Mississippi State...which are present during combustion (10). There is a...diesel particulates and coal combustion complicates the identification......

V.F. Kalasinsky; C. Saiwan; K.G. Whitehead

1988-11-01T23:59:59.000Z

39

A nitrate sink in estuaries?  

Science Journals Connector (OSTI)

and d15N and d18O of nitrate along the salinity gradient in the estuary of the river Elbe, one of the largest German rivers discharging into the North Sea. Nitrate ...

2008-06-04T23:59:59.000Z

40

Combustion of viscous hydrocarbons  

SciTech Connect

A method is described for utilizing viscous hydrocarbons as combustible fuels comprising: (A) forming a hydrocarbosol using a surfactant package in a proportion of about 1:100 to about 1:20,000 by weight based on hydrocarbon, (1) the surfactant package comprising (a) at least one water-soluble surfactant, an effective amount of which surfactant promotes emulsification of a hydrocarbon with API gravity of about 20/sup 0//sup o/ API or less; and (b) at least one water-soluble bioemulsifier, being a microboally-derived substance which predominantly resides at hydrocarbon/water interfaces to substantially surround hydrocarbon droplets in hydrocarbon-in-water emulsions; (2) the hydrocarbosol (a) comprising a hydrocarbon characterized by an API gravity of about 20/sup 0//sup o/ API or less; (b) having a hydrocarbon:water ratio of about 70:30 by volume; and (B) burning the resultant hydrocarbosol.

Hayes, M.E.; Hrebenar, K.R.; Murphy, P.L.; Futch, L.E. Jr.; Deal, J.F. III

1986-10-21T23:59:59.000Z

Note: This page contains sample records for the topic "hydrocarbons alkyl nitrates" 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

Purification of alkali metal nitrates  

DOE Patents (OSTI)

A process is disclosed for removing heavy metal contaminants from impure alkali metal nitrates containing them. The process comprises mixing the impure nitrates with sufficient water to form a concentrated aqueous solution of the impure nitrates, adjusting the pH of the resulting solution to within the range of between about 2 and about 7, adding sufficient reducing agent to react with heavy metal contaminants within said solution, adjusting the pH of the solution containing reducing agent to effect precipitation of heavy metal impurities and separating the solid impurities from the resulting purified aqueous solution of alkali metal nitrates. The resulting purified solution of alkali metal nitrates may be heated to evaporate water therefrom to produce purified molten alkali metal nitrate suitable for use as a heat transfer medium. If desired, the purified molten form may be granulated and cooled to form discrete solid particles of alkali metal nitrates.

Fiorucci, Louis C. (Hamden, CT); Gregory, Kevin M. (Woodridge, IL)

1985-05-14T23:59:59.000Z

42

Highly Effective Gene Transfection In Vivo by Alkylated Polyethylenimine  

E-Print Network (OSTI)

We mechanistically explored the effect of increased hydrophobicity of the polycation on the efficacy and specificity of gene delivery in mice. N-Alkylated linear PEIs with varying alkyl chain lengths and extent of substitution ...

Fortune, Jennifer A.

43

Catalytic Synthesis of n-Alkyl Arenes through Alkyl Group Cross-Metathesis  

E-Print Network (OSTI)

n-Alkyl arenes were prepared in a one-pot tandem dehydrogenation/olefin metathesis/hydrogenation sequence directly from alkanes and ethylbenzene. Excellent selectivity was observed when (tBuPCP)IrH[subscript 2] was paired ...

Dobereiner, Graham E.

44

Combustion of viscous hydrocarbons  

SciTech Connect

A method is described for utilizing viscous hydrocarbons as combustible pre-atomized fuels, comprising: (A) forming a hydrocarbon-in-water emulsion using an effective amount of a surfactant package comprising at least one water-soluble surfactant, the hydrocarbon-in-water emulsion (1) comprising a hydrocarbon characterized by API gravity of about 20/sup 0/ API or less, viscosity of about 1000 centipoise or greater at 212/sup 0/F., a paraffin content of about 50% by weight or less and, an aromatic content of about 15% by weight or greater, and (2) having a hydrocarbon water ratio from about 60:40 to about 90:10 by volume; and (B) burning the resultant hydrocarbon-in-water emulsion.

Hayes, M.E.; Hrebenar, K.R.; Murphy, P.L.; Futch, L.E. Jr.; Deal, J.F. III; Bolden, P.L. Jr.

1987-08-04T23:59:59.000Z

45

Detonation of Ammonium Nitrate Fertilizer  

Science Journals Connector (OSTI)

Detonation of Ammonium Nitrate Fertilizer ... charge of the fertilizer enclosed in ¼-inch Shelby seamless tubing, 3 inches in diameter and 20 inches in length, detonated with extreme violence. ...

1947-07-28T23:59:59.000Z

46

Hydrocarbon Potential of Deep Water  

Science Journals Connector (OSTI)

...research-article Hydrocarbon Potential of Deep Water H. R. Warman In...the geology and hydrocarbon potential of the Earth's deeper water areas, an attempt...United Kingdom 1981 Hydrocarbon potential of deep water Warman H. R. Author...

1978-01-01T23:59:59.000Z

47

Direct Evidence for a Marine Source of C1 and C2 Alkyl Nitrates  

Science Journals Connector (OSTI)

...samples, were pumped into 3-liter...under running seawater. Air samples...linearity, and storage artefacts were...out, in which seawater samples were...samples, were pumped into 3-liter...under running seawater. Air samples...linearity, and storage artefacts were...

Adele L. Chuck; Suzanne M. Turner; Peter S. Liss

2002-08-16T23:59:59.000Z

48

Alkyl nitrate (C 1 -C 3 ) depth profiles in the tropical Pacific Ocean  

E-Print Network (OSTI)

Experiment (WOCE), vol. 2, Pacific Ocean DRAFT, edited by M.over the equatorial Pacific Ocean during SAGA 3, J. Geophys.the troposphere over the Pacific Ocean during PEM- Tropics A

Dahl, E. E; Yvon-Lewis, S. A; Saltzman, E. S

2007-01-01T23:59:59.000Z

49

Recovering hydrocarbons from hydrocarbon-containing vapors  

DOE Patents (OSTI)

Values are recovered from a hydrocarbon-containing vapor by contacting the vapor with quench liquid consisting essentially of hydrocarbons to form a condensate and a vapor residue, the condensate and quench fluid forming a combined liquid stream. The combined liquid stream is mixed with a viscosity-lowering liquid to form a mixed liquid having a viscosity lower than the viscosity of the combined liquid stream to permit easy handling of the combined liquid stream. The quench liquid is a cooled portion of the mixed liquid. Viscosity-lowering liquid is separated from a portion of the mixed liquid and cycled to form additional mixed liquid.

Mirza, Zia I. (La Verne, CA); Knell, Everett W. (Los Alamitos, CA); Winter, Bruce L. (Danville, CA)

1980-09-30T23:59:59.000Z

50

A Detailed Chemical Kinetic Reaction Mechanism for Oxidation of Four Small Alkyl Esters in Laminar Premixed Flames  

SciTech Connect

A detailed chemical kinetic reaction mechanism has been developed for a group of four small alkyl ester fuels, consisting of methyl formate, methyl acetate, ethyl formate and ethyl acetate. This mechanism is validated by comparisons between computed results and recently measured intermediate species mole fractions in fuel-rich, low pressure, premixed laminar flames. The model development employs a principle of similarity of functional groups in constraining the H atom abstraction and unimolecular decomposition reactions in each of these fuels. As a result, the reaction mechanism and formalism for mechanism development are suitable for extension to larger oxygenated hydrocarbon fuels, together with an improved kinetic understanding of the structure and chemical kinetics of alkyl ester fuels that can be extended to biodiesel fuels. Variations in concentrations of intermediate species levels in these flames are traced to differences in the molecular structure of the fuel molecules.

Westbrook, C K; Pitz, W J; Westmoreland, P R; Dryer, F L; Chaos, M; Osswald, P; Kohse-Hoinghaus, K; Cool, T A; Wang, J; Yang, B; Hansen, N; Kasper, T

2008-02-08T23:59:59.000Z

51

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

52

E-Print Network 3.0 - alkyl-tert alkyl ethers Sample Search Results  

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

> >> 1 7198 J. Org. Chem. 1995,60, 7198-7208 Gas Phase Decomposition of Conjugate Acid Ions of Simple Summary: of ProtonatedAlkyl tert-ButylEthers RO(H)C(CH&+ (To.6 Values in meV...

53

Sensitive Analysis of Alkyl Alcohols as Decomposition Products of Alkyl Nitrites in Human Whole Blood and Urine by Headspace Capillary GC with Cryogenic Oven Trapping  

Science Journals Connector (OSTI)

......cryogenic oven trapping. | The abuse of alkyl nitrites is becoming...Sensitivity and Specificity The abuse of alkyl nitrites is becoming...them at common markets or by internet sales. The most popular alkyl...the detection of alkyl nitrite abuse in forensic science practice......

Kanako Watanabe-Suzuki; Robert R. Lemmer; Hideki Nozawa; Osamu Suzuki; Akira Ishii

2003-02-01T23:59:59.000Z

54

Alkyl Surface Treatments of Planar Zinc Oxide in Hybrid Organic/Inorganic Solar Cells  

SciTech Connect

Hybrid organic/inorganic solar cells have not lived up to their potential because of poor interface properties. Interfacial molecular layers provide a way of adjusting these devices to improve their performance. We have studied a prototypical system involving poly(3-hexylthiophene) (P3HT) on planar zinc oxide (ZnO) films that have been modified with two types of molecules having identical 18-carbon alkyl chain termination and different surface attachments: octadecanethiol (ODT) and octadecyltriethoxysilane (OTES). We examined the functionalized surfaces using water contact angle measurements, Kelvin probe measurements, infrared absorbance spectroscopy, and atomic force microscopy. These have shown that OTES forms disordered incomplete monolayers, while ODT is prone to develop multilayered islands. Both treatments enhance polymer ordering. However, inverted solar cell devices fabricated with these treated interfaces performed very differently. ODT improves the short circuit current (J{sub SC}), open circuit voltage (V{sub OC}), and power conversion efficiency ({eta}), while these parameters all decrease in devices constructed from OTES-treated ZnO. The differences in V{sub OC} are related to modifications of the surface dipole associated with deposition of the two types of alkyl molecules, while changes in J{sub SC} are attributed to a balance between charge transfer blocking caused by the saturated hydrocarbon and the improved hole mobility in the polymer.

Allen, C. G.; Baker, D. J.; Brenner, T. M.; Weigand, C. C.; Albin, J. M.; Steirer, K. X.; Olson, D. C.; Ladam, C.; Ginley, D. S.; Collins, R. T.; Furtak, T. E.

2012-04-26T23:59:59.000Z

55

Role of methyl nitrate in plasma exhaust treatment  

SciTech Connect

There is growing interest in the use of a nonthermal plasma combined with a catalyst for NO{sub x} removal from diesel engine exhaust streams. Such exhaust streams contain excess oxygen (typically 6--10%), low concentrations of hydrocarbons (typically 100--1,000 ppm), and significant concentrations of water (typically 5--12%). Conversion of NO{sub x} to environmentally acceptable compounds, without requiring a scrubber or an added reductant, is the desired end result. In their research the authors observe the formation of substantial amounts of methyl nitrate (CH{sub 3}ONO{sub 2}) in the plasma-catalyst system. CH{sub 3}ONO{sub 2} was prepared and added to the gas blend on test equipment simulating a diesel exhaust gas. A dielectric barrier plasma discharge was followed by a zeolite-based catalyst. Methyl nitrate introduced upstream of the plasma discharge is largely unreacted upon passing through the plasma. CH{sub 3}ONO{sub 2} arriving at the catalyst is converted to methanol and NO{sub 2}. While methyl nitrate was shown to be formed in this system, it is not a significant intermediate in the mechanism of conversion of NO{sub x} to nitrogen.

Hoard, J.W.; Wallington, T.J.; Ball, J.C.; Hurley, M.D.; Wodzisz, K.; Balmer, M.L.

1999-10-01T23:59:59.000Z

56

Distribution of Pendant Alkyl Groups in the Argonne Premium Coals  

Science Journals Connector (OSTI)

Distribution of Pendant Alkyl Groups in the Argonne Premium Coals ... Chemistry Division, Argonne National Laboratory, Argonne, Illinois 60439, and Department of Chemistry, The University of Chicago, Chicago, Illinois 60637 ... The ruthenium(VIII) oxidation reaction has been employed to determine the distribution of alkyl groups that are bonded to aromatic structural elements in lignin and the Argonne Premium Coals. ...

Marcus Obeng; Leon M. Stock

1996-07-18T23:59:59.000Z

57

E-Print Network 3.0 - alkyl amides derivatives Sample Search...  

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

allylic alkylation Summary: Highly ecient kinetic resolution of 2-cyclohexenyl acetate in Pd-catalyzed allylic alkylation James... been synthesized and employed in the...

58

E-Print Network 3.0 - alkyl chain bending Sample Search Results  

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

interacting alkyl substituents Source: Collection: Chemistry 74 Low absorption liquid crystals for mid-wave infrared applications Summary: (), while keeping the alkyl chain...

59

Dispersant solutions for dispersing hydrocarbons  

DOE Patents (OSTI)

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

Tyndall, R.L.

1997-03-11T23:59:59.000Z

60

Carbon neutral hydrocarbons  

Science Journals Connector (OSTI)

...depends on a source of primary energy to drive the required chemical...synthetic hydrocarbons are an energy carrier produced from a primary energy source such as wind, nuclear...Gustavsson et al. 2007), using a conversion value of $1.00=0.72...

2008-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "hydrocarbons alkyl nitrates" 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

Optrode for sensing hydrocarbons  

DOE Patents (OSTI)

A two-phase system employing the Fujiwara reaction is provided for the fluorometric detection of halogenated hydrocarbons. A fiber optic is utilized to illuminate a column of pyridine trapped in a capillary tube coaxially attached at one end to the illuminating end of the fiber optic. A strongly alkaline condition necessary for the reaction is maintained by providing a reservoir of alkali in contact with the column of pyridine, the surface of contact being adjacent to the illuminating end of the fiber optic. A semipermeable membrane caps the other end of the capillary tube, the membrane being preferentially permeable to the halogenated hydrocarbon and but preferentially impermeable to water and pyridine. As the halogenated hydrocarbon diffuses through the membrane and into the column of pyridine, fluorescent reaction products are formed. Light propagated by the fiber optic from a light source, excites the fluorescent products. Light from the fluorescence emission is also collected by the same fiber optic and transmitted to a detector. The intensity of the fluorescence gives a measure of the concentration of the halogenated hydrocarbons.

Miller, Holly (Bethel Island, CA); Milanovich, Fred P. (Lafayette, CA); Hirschfeld, Tomas B. (Livermore, CA); Miller, Fred S. (Bethel Island, CA)

1987-01-01T23:59:59.000Z

62

Optrode for sensing hydrocarbons  

DOE Patents (OSTI)

A two-phase system employing the Fujiwara reaction is provided for the fluorometric detection of halogenated hydrocarbons. A fiber optic is utilized to illuminate a column of pyridine trapped in a capillary tube coaxially attached at one end to the illuminating end of the fiber optic. A strongly alkaline condition necessary for the reaction is maintained by providing a reservoir of alkali in contact with the column of pyridine, the surface of contact being adjacent to the illuminating end of the fiber optic. A semipermeable membrane caps the other end of the capillary tube, the membrane being preferentially permeable to the halogenated hydrocarbon and but preferentially impermeable to water and pyridine. As the halogenated hydrocarbon diffuses through the membrane and into the column of pyridine, fluorescent reaction products are formed. Light propagated by the fiber optic from a light source, excites the fluorescent products. Light from the fluorescence emission is also collected by the same fiber optic and transmitted to a detector. The intensity of the fluorescence gives a measure of the concentration of the halogenated hydrocarbons. 5 figs.

Miller, H.; Milanovich, F.P.; Hirschfeld, T.B.; Miller, F.S.

1988-09-13T23:59:59.000Z

63

Optrode for sensing hydrocarbons  

DOE Patents (OSTI)

A two-phase system employing the Fujiwara reaction is provided for the fluorometric detection of halogenated hydrocarbons. A fiber optic is utilized to illuminate a column of pyridine trapped in a capillary tube coaxially attached at one end to the illuminating end of the fiber optic. A strongly alkaline condition necessary for the reaction is maintained by providing a reservoir of alkali in contact with the column of pyridine, the surface of contact being adjacent to the illuminating end of the fiber optic. A semipermeable membrane caps the other end of the capillary tube, the membrane being preferentially permeable to the halogenated hydrocarbon but preferentially impermeable to water and pyridine. As the halogenated hydrocarbon diffuses through the membrane and into the column of pyridine, fluorescent reaction products are formed. Light propagated by the fiber optic from a light source, excites the fluorescent products. Light from the fluorescence emission is also collected by the same fiber optic and transmitted to a detector. The intensity of the fluorescence gives a measure of the concentration of the halogenated hydrocarbons. 6 figs.

Miller, H.; Milanovich, F.P.; Hirschfeld, T.B.; Miller, F.S.

1987-05-19T23:59:59.000Z

64

Optrode for sensing hydrocarbons  

DOE Patents (OSTI)

A two-phase system employing the Fujiwara reaction is provided for the fluorometric detection of halogenated hydrocarbons. A fiber optic is utilized to illuminate a column of pyridine trapped in a capillary tube coaxially attached at one end to the illuminating end of the fiber optic. A strongly alkaline condition necessary for the reaction is maintained by providing a reservoir of alkali in contact with the column of pyridine, the surface of contact being adjacent to the illuminating end of the fiber optic. A semipermeable membrane caps the other end of the capillary tube, the membrane being preferentially permeable to the halogenated hydrocarbon and but preferentially impermeable to water and pyridine. As the halogenated hydrocarbon diffuses through the membrane and into the column of pyridine, fluorescent reaction products are formed. Light propagated by the fiber optic from a light source, excites the fluorescent products. Light from the fluorescence emission is also collected by the same fiber optic and transmitted to a detector. The intensity of the fluorescence gives a measure of the concentration of the halogenated hydrocarbons.

Miller, Holly (Bethel Island, CA); Milanovich, Fred P. (Lafayette, CA); Hirschfeld, Tomas B. (Livermore, CA); Miller, Fred S. (Bethel Island, CA)

1988-01-01T23:59:59.000Z

65

A Novel Chemical Nitrate Destruction Process  

SciTech Connect

Nitrates represent one of the most significant pollutant discharged to the Baltic Sea by the Sliiamae hydrometallurgical plant. This article contains a brief overview of the existing nitrate destruction technologies followed by the description of a new process developed by the authors. The new chemical process for nitrate destruction is cost effective and simple to operate. It converts the nitrate to nitrogen gas which goes to the atmosphere.

Dziewinski, J.; Marczak, S.

1999-03-01T23:59:59.000Z

66

Final Technical Report [Development of Catalytic Alkylation and Fluoroalkylation Methods  

SciTech Connect

In the early stages of this DOE-funded research project, we sought to prepare and study a well-defined nickel-alkyl complex containing tridentate nitrogen donor ligands. We found that reaction of (TMEDA)NiMe2 (1) with terpyridine ligand cleanly led to the formation of (terpyridyl)NiMe (2), which we also determined to be an active alkylation catalyst. The thermal stability of 2 was unlike that seen for any of the active pybox ligands, and enabled a number of key studies on alkyl transfer reactions to be performed, providing new insights into the mechanism of nickel-mediated alkyl-alkyl cross-coupling reactions. In addition to the mechanistic studies, we showed that the terpyridyl nickel compounds can catalytically cross-couple alkyl iodides in yields up to 98% and bromides in yields up to 46 %. The yields for the bromides can be increased up to 67 % when the new palladium catalyst [(tpy’)Pd-Ph]I is used. The best route to the targeted [(tpy)NiBr] (1) was found to involve the comproportionation reaction of [(dme)NiBr{sub 2}] and [Ni(COD){sub 2}] in the presence of two equivalents of terpyridine. This reaction was driven to high yields of product formation (72 % isolated) by the precipitation of 1 from THF solvent.

Vicic, David A.

2014-05-01T23:59:59.000Z

67

THERMOCHEMISTRY OF HYDROCARBON RADICALS  

SciTech Connect

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

68

Radical scavengers from heavy hydrocarbons  

SciTech Connect

The hydrogen-donating properties of some hydrocarbons form the basis for processes such as coal liquefaction and heavy oil upgrading. However, these hydrocarbons have seldom been used for other purposes, because their potential applications have not been well recognized. Research has indicated that these hydrogen-donating hydrocarbons can be used in important reactions as radical scavengers and have properties particular to those of pure hydrocarbons without functional groups containing heteroatoms. Over years of study researchers have found that pure hydrocarbons with radical-scavenging effects nearly as high as those in conventional hindered phenolic antioxidants can be produced from petroleum, and these hydrogen-donating hydrocarbons exhibit such effects even in oxidative atmospheres (i.e., they function as antioxidants). He has also shown that these mixtures have some properties particular to pure hydrocarbons without functional groups containing heteroatoms, and they`ve seen that a mechanism based on the steric effects appears when these hydrocarbons are used in heavy oil hydroprocessing. Hydrogen-donating hydrocarbons should be a viable resource in many applications. In this article, he presents radical-scavenging abilities, characteristics as pure hydrocarbons, and applications on the basis of the studies.

Kubo, Junichi [Nippon Oil Co. Ltd. (Japan)

1996-10-01T23:59:59.000Z

69

Sensitive Analysis of Alkyl Alcohols as Decomposition Products of Alkyl Nitrites in Human Whole Blood and Urine by Headspace Capillary GC with Cryogenic Oven Trapping  

Science Journals Connector (OSTI)

......470-1192, Japan The abuse of alkyl nitrites is...oven trapping. | The abuse of alkyl nitrites is...Sensitivity and Specificity The abuse of alkyl nitrites is...abused by inhalation among young people for their aphrodisiac...common markets or by internet sales. The most popular......

Kanako Watanabe-Suzuki; Robert R. Lemmer; Hideki Nozawa; Osamu Suzuki; Akira Ishii

2003-02-01T23:59:59.000Z

70

Potential of producing various hydrocarbons from canola oil by catalytic treatment over Pt-ZSM-5  

SciTech Connect

Canola oil conversion was studied at atmospheric pressure over Pt-ZSM-5 catalyst (0.5 wt% Pt) in a fixed bed micro-reactor. The operating conditions were: temperature range of 400--500 C, weight hourly space velocity (WHSV) of 1.8 and 3.6 h{sup {minus}1} and steam/oil ratio of 4:1. The products were coke, gas, an organic liquid product (OLP) and residue. The gas and OLP consisted mainly of hydrocarbons. The objective of this study was to maximize the amount of gasoline range hydrocarbons in the OLP and the selectivity to isohydrocarbons in the gas. The gas yields varied between 22--65 wt% and were higher in the presence of steam compared to the operation without steam. Also, the gas fraction decreased with increase in space velocity. The olefin/paraffin ratio of C{sub 2}-C{sub 4} hydrocarbon gases varied between 0.31--0.79. The amount of isohydrocarbons relative to n-hydrocarbons were higher with Pt-ZSM-5 (1.6--4.8) compared to pure HZSM-5 catalyst (0.2--0.3). The OLP yields with Pt-ZSM-5 (20--55wt% of canola oil) were slightly lower compared to HZSM-5 (40--63wt% of canola oil) under similar conditions. The major components of OLP were aliphatic and aromatic hydrocarbons. The main aromatic hydrocarbons were benzene, toluene, xylenes and trimethylbenzenes. Alkylated pentane and hexane were the main aliphatic hydrocarbons. In the presence of steam, Pt-ZSM-5 gave higher yields of liquid hydrocarbons within the gasoline boiling range than HZSM-5.

Katikaneni, S.P.R.; Adjaye, J.D.; Bakhshi, N.N. [Univ. of Saskatchewan, Saskatoon (Canada)

1995-12-31T23:59:59.000Z

71

The Utilization of Certain Hydrocarbons by Microorganisms  

Science Journals Connector (OSTI)

...UTILIZATION OF CERTAIN HYDROCARBONS BY MICROORGANISMS...1940 INTRODUCTION Hydrocarbons, as a class, represent...obtained by comparing the heat of combustion of some six carbon...biological utilization of hydrocarbons as sources of energy...

L. D. Bushnell; H. F. Haas

1941-05-01T23:59:59.000Z

72

Interaction between Carcinogenic Hydrocarbons and Nucleosides  

Science Journals Connector (OSTI)

...addition, the findings that hydrocarbons inhibit DNA syn thesis...for these carcinogens. Hydrocarbon-nucleic acid interaction...and the interactions of water molecules. Indeed, carcinogenic hydrocarbons tend to form 1 This investigation...

Ronald G. Harvey and Marilyn Halonen

1968-11-01T23:59:59.000Z

73

Enhanced liquid hydrocarbon recovery process  

SciTech Connect

This patent describes a process for recovering liquid hydrocarbons. It comprises: injecting into a fractured subterranean formation a polymer enhanced foam comprising a polymer selected from a synthetic polymer or a biopolymer, a surfactant, an aqueous solvent and a gas, recovering liquid hydrocarbons from the formation.

Sydansk, R.D.

1992-07-14T23:59:59.000Z

74

Hydrocarbon sensors and materials therefor  

DOE Patents (OSTI)

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

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

2000-01-01T23:59:59.000Z

75

The infrared and Raman spectra of N-alkyl ethylenimines  

E-Print Network (OSTI)

mother, without wnose sacrifices and help none of this would have been possible. TABLE OF CONTLNTS THE INFPAR D AND P'u~'AN SP" CTPW OF N-ALKYL ETHYLENIYINES Pa8e I. Introduction. . . . , . . . . , II. Experimental. . . , . 3 III ' Discussion... be represented as follows, CH2 R ? ~ &CH 2 where R = CH3-, C2H5-, and (CH3)2CH-. It is assumed here that the alkyl group lies above the plane of the ring as does the N-H hydrogen in ethylenimine. ' ' This assumption has been supported 8 9, 11 in the case...

Ashby, Theodore Leroy

2012-06-07T23:59:59.000Z

76

E-Print Network 3.0 - allylic alkylations added Sample Search...  

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

benzyl or allyl halides. s-Alkyl... -chiral center of high optical purity based on the SN2 displace- ment reaction of alkyl cuprates on chiral allyl... A Practical and Highly...

77

E-Print Network 3.0 - asymmetric allylic alkylation Sample Search...  

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

benzyl or allyl halides. s-Alkyl... -chiral center of high optical purity based on the SN2 displace- ment reaction of alkyl cuprates on chiral allyl... ) Examples of asymmetric...

78

Alcohol Chemistry on Rutile TiO2(110): The Influence of Alkyl...  

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

Alcohol Chemistry on Rutile TiO2(110): The Influence of Alkyl Substituents on Reactivity and Selectivity. Alcohol Chemistry on Rutile TiO2(110): The Influence of Alkyl Substituents...

79

Process for recovering hydrocarbons from a hydrocarbon-bearing formation  

SciTech Connect

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

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

1980-03-11T23:59:59.000Z

80

Highly Enantioselective sec-Alkyl Sulfatase Activity of Sulfolobus acidocaldarius DSM 639  

Science Journals Connector (OSTI)

Highly Enantioselective sec-Alkyl Sulfatase Activity of Sulfolobus acidocaldarius DSM 639 ... rac-sec-Alkyl sulfate esters 1a?4a were resolved in high enantioselectivities with E-values up to >200 using whole cells of aerobically grown Sulfolobus acidocaldarius DSM 639. ... On the basis of vague hints on the stereospecific and enantioselective hydrolysis of alkyl sulfate esters,3 we recently reported an alkyl sulfatase (termed “RS2”) from Rhodococcus ruber DSM 44541. ...

Sabine R. Wallner; Bettina M. Nestl; Kurt Faber

2004-12-02T23:59:59.000Z

Note: This page contains sample records for the topic "hydrocarbons alkyl nitrates" 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

Nitrates and Prussic Acid in Forages  

E-Print Network (OSTI)

When nitrates and prussic acid accumulate in forage, the feed may not be safe for livestock consumption. Learn the symptoms of nitrate and prussic acid poisoning and which plants are most likely to pose a risk to livestock. Also learn sampling...

Provin, Tony; Pitt, John L.

2003-01-06T23:59:59.000Z

82

Nitrate removal from drinking water -- Review  

SciTech Connect

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

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

1997-04-01T23:59:59.000Z

83

Microbial degradation of n-alkyl tetrahydrothiophenes found in petroleum  

SciTech Connect

Although n-alkyl-substituted tetrahydrothiophenes are found in nonbiodegraded petroleums, they are not found in petroleums which have undergone biodegradation in their reservoirs. These observations suggested that this group of compounds with alkyl chain lengths from approximately C/sub 10/ to at least C/sub 30/ is biodegradable. Two of these sulfides, 2-n-dodecyltetrahydrothiophene (DTHT) and 2-n-undecyltetrahydrothiophene, were synthesized, and their biodegradabilities were tested by using five gram-positive, n-alkane-degrading bacterial isolates. The alkyl side chains of these compounds were oxidized, and the major intermediates found in 2-n-undecyltetrahydrothiophene- and DTHT-metabolizing cultures were 2-tetrahydrothiophenecarboxylic acid (THTC) and 2-tetrahydrothiopheneacetic acid (THTA), respectively. Four n-alkane-degrading fungi were also shown to degrade DTHT, yielding both THTA and THTC. Quantitation of tetrahydrothiophene ring-containing products in 28-day-old bacterial and fungal cultures suggested that THTC and THTA were metabolized further to unidentified products. In addition, two of the bacterial isolates were shown to degrade a mixture of n-alkyl tetrahydrothiophenes isolated from Bellshill Lake crude oil.

Fedorak, P.M.; Payzant, J.D.; Montgomery, D.S.; Westlake, D.W.S.

1988-05-01T23:59:59.000Z

84

Alkylation of Guanosine and Deoxyguanosine by Phosphoramide Mustard  

Science Journals Connector (OSTI)

...Phosphoramide mustard, an active metabolite of cyclophosphamide...Phosphoramide mustard, an active metabolite of cyclophos...acrolein (1) and an active alkylating agent, phosphoramide...adducts which it forms. MATERIALS AND METHODS Crystalline...field emitter anode and cathode; 8 kV acceler ating...

Jitendra R. Mehta; Michael Przybylski; and David B. Ludlum

1980-11-01T23:59:59.000Z

85

Reactions Between Water Soluble Organic Acids and Nitrates in...  

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

Between Water Soluble Organic Acids and Nitrates in Atmospheric Aerosols: Recycling of Nitric Acid and Formation of Reactions Between Water Soluble Organic Acids and Nitrates in...

86

Report seeks solutions for nitrate in drinking water  

E-Print Network (OSTI)

Nitrate in California’s Drinking Water report http://Clark Report seeks solutions for nitrate in drinking waternitrate contamination of drinking water in high-risk areas

Editors, By

2012-01-01T23:59:59.000Z

87

The seasonal evolution of NMHCs and light alkyl nitrates at middle to high northern latitudes during TOPSE  

E-Print Network (OSTI)

Meinardi,1 Oliver W. Wingenter,3 Elliot L. Atlas,4 Frank Flocke,4 Brian A. Ridley,4 and F. Sherwood Rowland with meteorological trajectory analysis, different trace gas signatures provided significant clues to the origins here provide a unique picture of NH trace gas evolution from winter to summer that will be invaluable

Wingenter, Oliver W.

88

A new technology for producing synthetic liquid hydrocarbons from gaseous hydrocarbons  

Science Journals Connector (OSTI)

Conventional technologies of synthetic liquid fuels (SLF) production from gaseous hydrocarbons by producing synthesis ... liquid hydrocarbons are examined. A high-efficiency SLF production technology that allows ...

D. L. Astanovskii; L. Z. Astanovskii; A. L. Lapidus

2012-09-01T23:59:59.000Z

89

Synthesis of a new energetic nitrate ester  

SciTech Connect

Nitrate esters have been known as useful energetic materials since the discovery of nitroglycerin by Ascanio Sobrero in 1846. The development of methods to increase the safety and utility of nitroglycerin by Alfred Nobel led to the revolutionary improvement in the utility of nitroglycerin in explosive applications in the form of dynamite. Since then, many nitrate esters have been prepared and incorporated into military applications such as double-based propellants, detonators and as energetic plasticizers. Nitrate esters have also been shown to have vasodilatory effects in humans and thus have been studied and used for treatments of ailments such as angina. The mechanism of the biological response towards nitrate esters has been elucidated recently. Interestingly, many of the nitrate esters used for military purposes are liquids (ethylene glycol dinitrate, propylene glycol dinitrate, etc). Pentaerythritol tetranitrate (PETN) is one of the only solid nitrate esters, besides nitrocellulose, that is used in any application. Unfortunately, PETN melting point is above 100 {sup o}C, and thus must be pressed as a solid for detonator applications. A more practical material would be a melt-castable explosive, for potential simplification of manufacturing processes. Herein we describe the synthesis of a new energetic nitrate ester (1) that is a solid at ambient temperatures, has a melting point of 85-86 {sup o}C and has the highest density of any known nitrate ester composed only of carbon, hydrogen, nitrogen and oxygen. We also describe the chemical, thermal and sensitivity properties of 1 as well as some preliminary explosive performance data.

Chavez, David E [Los Alamos National Laboratory

2008-01-01T23:59:59.000Z

90

Enrichment of light hydrocarbon mixture  

DOE Patents (OSTI)

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

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

2011-11-29T23:59:59.000Z

91

Biological enhancement of hydrocarbon extraction  

DOE Patents (OSTI)

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

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

2009-01-06T23:59:59.000Z

92

Fluorescence Detection of Hydrocarbons in Harbour Water  

Science Journals Connector (OSTI)

In harbor water, the hydrocarbons pollution identification represents an important issue. Hydrocarbon presence derives from oil spills, for instance in bilge water, or it may come from industrial discharge ... Fl...

A. Catini; F. Dini; D. Polese; S. Petrocco; M. De Luca…

2011-01-01T23:59:59.000Z

93

Estimating The Thermodynamics And Kinetics Of Chlorinated Hydrocarbon...  

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

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

94

Extracting hydrocarbons from water using a centrifuge  

Science Journals Connector (OSTI)

An original method for the solid-phase microextraction of hydrocarbons from water using a centrifuge is proposed. Comparative results...

A. Yu. Ryabov; A. A. Ilyina; A. V. Chuikin…

2014-09-01T23:59:59.000Z

95

Photo-oxides of Carcinogenic Hydrocarbons  

Science Journals Connector (OSTI)

... are involved in the biological action of carcinogenic hydrocarbons, we have attempted to isolate the photo-oxides of some of these hydrocarbons. Such ... -oxides of some of these hydrocarbons. Such photo-oxides would naturally be insoluble in water and hence would represent merely one stage in ...

J. W. COOK; R. MARTIN; E. M. F. ROE

1939-06-17T23:59:59.000Z

96

Catalytic steam reforming of hydrocarbons  

SciTech Connect

The hot effluent from the catalytic steam reforming of a major portion of a fluid hydrocarbon feed stream in the reformer tubes of a primary reformer, or said effluent after secondary reforming thereof, is mixed with the hot effluent from the catalytic steam reforming of the remaining portion of the feed discharged from the reformer tubes of a primary reformer-exchanger. The combined gas steam is passed on the shell side of the reformer-exchanger countercurrently to the passage of feed in the reformer tubes thereof, thus supplying the heat for the reforming of the portion of the feed passed through the reformer tubes of the reformerexchanger. At least about 2/3 of the hydrocarbon feed stream is passed to the reformer tubes of said primary reformer, heated by radiant heat transfer and/or by contact with combustion gases, at a steam/hydrocarbon mole ratio of about 2-4/1. The remainder of said feed stream is passed to the reformer tubes of said reformer -exchanger at a steam/hydrocarbon mole ratio of about 3-6/1. The reformer shell of the reformer-exchanger is internally insulated by a refractory lining or by use of a double shell with passage of water or a portion of the feed material between the inner and outer shells. There is no significant difference between the pressure inside and outside of the reformer tubes of said primary reformer-exchanger.

Fuderer, A.

1982-06-29T23:59:59.000Z

97

E-Print Network 3.0 - alkylating agents synthesis Sample Search...  

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

Natural Product Leinamycin Summary: , the antitumor natural product leina- mycin (LM) (1, 2) is converted to a potent DNA-alkylating agent via... the sequence specificity...

98

E-Print Network 3.0 - alkylating agents Sample Search Results  

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

Natural Product Leinamycin Summary: , the antitumor natural product leina- mycin (LM) (1, 2) is converted to a potent DNA-alkylating agent via... the sequence specificity...

99

E-Print Network 3.0 - alkylating agents evaluacion Sample Search...  

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

Natural Product Leinamycin Summary: , the antitumor natural product leina- mycin (LM) (1, 2) is converted to a potent DNA-alkylating agent via... the sequence specificity...

100

Syngas Upgrading to Hydrocarbon Fuels Technology Pathway  

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

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.

Note: This page contains sample records for the topic "hydrocarbons alkyl nitrates" 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

Nickel-catalyzed Suzuki-Miyaura reactions of unactivated halides with alkyl boranes and planar-chiral borabenzene catalysts for Diels-Alder reactions  

E-Print Network (OSTI)

Part I describes the expansion in scope of a nickel-catalyzed coupling reaction of unactivated alkyl bromides and alkyl boranes to include unactivated alkyl chlorides. The new method is adapted for use outside of a glove ...

Lu, Zhe

2010-01-01T23:59:59.000Z

102

Perchlorate and nitrate in situ bioremediation of ground water  

SciTech Connect

Nitrate and perchlorate are growing worldwide problems as mobile anionic groundwater contaminants. Biological rduction of nitrate and perchlorate in groundwater is under development as a technology to address these problems.

Strietelmeier, E. A. (Elizabeth A.); Nuttall, H. Eric; Hatzinger, Paul; Goltz, Mark

2002-01-01T23:59:59.000Z

103

Denitration of High Nitrate Salts Using Reductants  

SciTech Connect

This report describes work conducted by Pacific Northwest National Laboratory (PNNL), in conjunction with Idaho National Engineering and Environmental Laboratory (INEEL), to remove nitrates in simulated low-activity waste (LAW). The major objective of this work was to provide data for identifying and demonstrating a technically viable and cost-effective approach to condition LAW for immobilization (grout).

HD Smith; EO Jones; AJ Schmidt; AH Zacher; MD Brown; MR Elmore; SR Gano

1999-05-03T23:59:59.000Z

104

3, 59195976, 2003 The nitrate aerosol  

E-Print Network (OSTI)

ACPD 3, 5919­5976, 2003 The nitrate aerosol field over Europe M. Schaap et al. Title Page Abstract of Utrecht, Institute of Marine and Atmospheric Science, PO Box 80005, 3508 TA, Utrecht, The Netherlands 2, The Netherlands 3 Netherlands Energy Research Foundation (ECN), PO Box 1, 1755 LE Petten, The Netherlands 4 Joint

Paris-Sud XI, Université de

105

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":""}]}

106

Enhanced liquid hydrocarbon recovery process  

SciTech Connect

This patent describes a process for the recovery of liquid hydrocarbons from a subterranean hydrocarbon-bearing formation. It comprises injecting natural gas into the formation via a well in fluid communication with the formation, the natural gas being at a temperature which is insufficient to significantly mobilize light density oil in the formation and at a pressure such that the natural gas is immiscible with the light density oil in the formation, the natural gas being injected in a volume sufficient to contact light density oil in the formation within a radius from the well of about 50 meters; shutting in the well for a period of time of about 1 to about 100 days which is sufficient to render the contacted light density oil mobile; and producing the light density oil which has been mobilized by solution of the natural gas from the well.

Haines, H.K.; Monger, T.G.; Kenyon, D.E.; Galvin, L.J.

1991-06-25T23:59:59.000Z

107

Dry reforming of hydrocarbon feedstocks  

SciTech Connect

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

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

2014-01-01T23:59:59.000Z

108

Chapter 3 - Hydrocarbons from Petroleum  

Science Journals Connector (OSTI)

Publisher Summary Petroleum products (in contrast to petrochemicals) are those hydrocarbon fractions that are derived from petroleum and have commercial value as a bulk product. A major group of hydrocarbon products from petroleum (petrochemicals) are the basis of a major industry. They are, in the strictest sense, different to petroleum products insofar as the petrochemicals are the basic building blocks of the chemical industry. The specific gravity of product gases, including liquefied petroleum gas, may be determined conveniently by a number of methods and a variety of instruments. The heat value of gases is generally determined at constant pressure in a flow calorimeter in which the heat released by the combustion of a definite quantity of gas is absorbed by a measured quantity of water or air. A continuous recording calorimeter is available for measuring heat values of natural gases.

James G. Speight

2011-01-01T23:59:59.000Z

109

Year/PAD District Alkylates Aromatics Road Oil  

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

Alkylates Alkylates Aromatics Road Oil and Lubricants Petroleum Coke (MMcfd) Hydrogen Sulfur (short tons/day) Production Capacity Asphalt Isomers Marketable Table 7. Operable Production Capacity of Petroleum Refineries, January 1, 1981 to January 1, 2013 (Thousand Barrels per Stream Day, Except Where Noted) a JAN 1, 1981 974 299 765 131 234 276 2,054 NA JAN 1, 1982 984 290 740 162 242 267 1,944 NA JAN 1, 1983 960 237 722 212 241 296 2,298 NA JAN 1, 1984 945 218 800 208 241 407 2,444 NA JAN 1, 1985 917 215 767 219 243 424 2,572 NA JAN 1, 1986 941 276 804 258 246 356 2,357 NA JAN 1, 1987 974 287 788 326 250 364 2,569 23,806 JAN 1, 1988 993 289 788 465 232 368 2,418 27,639 JAN 1, 1989 1,015 290 823 469 230 333 2,501 28,369 JAN 1, 1990 1,030 290 844 456 232 341 2,607 24,202

110

Discharge produces hydrocarbons from coal  

Science Journals Connector (OSTI)

Discharge produces hydrocarbons from coal ... Studies of the reactions of coal in electric discharges by two chemists at the U.S. Bureau of Mines' Pittsburgh Coal Research Center may lead to improved ways of producing acetylene and other useful chemicals from coal. ... Other workers have produced high yields of acetylene from coal by extremely rapid pyrolysis using energy sources such as plasma jets, laser beams, arc-image reactors, and flash heaters. ...

1968-01-22T23:59:59.000Z

111

Deep desulfurization of hydrocarbon fuels  

DOE Patents (OSTI)

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

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

2012-04-17T23:59:59.000Z

112

NITRATE DESTRUCTION LITERATURE SURVEY AND EVALUATION CRITERIA  

SciTech Connect

This report satisfies the initial phase of Task WP-2.3.4 Alternative Sodium Recovery Technology, Subtask 1; Develop Near-Tank Nitrate/Nitrite Destruction Technology. Some of the more common anions in carbon steel waste tanks at SRS and Hanford Site are nitrate which is corrosive, and nitrite and hydroxide which are corrosion inhibitors. At present it is necessary to periodically add large quantities of 50 wt% caustic to waste tanks. There are three primary reasons for this addition. First, when the contents of salt tanks are dissolved, sodium hydroxide preferentially dissolves and is removed. During the dissolution process the concentration of free hydroxide in the tank liquid can decrease from 9 M to less than 0.2 M. As a result, roughly half way through the dissolution process large quantities of sodium hydroxide must be added to the tank to comply with requirements for corrosion control. Second, hydroxide is continuously consumed by reaction with carbon dioxide which occurs naturally in purge air used to prevent buildup of hydrogen gas inside the tanks. The hydrogen is generated by radiolysis of water. Third, increasing the concentration of hydroxide increases solubility of some aluminum compounds, which is desirable in processing waste. A process that converts nitrate and nitrite to hydroxide would reduce certain costs. (1) Less caustic would be purchased. (2) Some of the aluminum solid compounds in the waste tanks would become more soluble so less mass of solids would be sent to High Level Vitrification and therefore it would be not be necessary to make as much expensive high level vitrified product. (3) Less mass of sodium would be fed to Saltstone at SRS or Low Level Vitrification at Hanford Site so it would not be necessary to make as much low level product. (4) At SRS less nitrite and nitrate would be sent to Defense Waste Processing Facility (DWPF) so less formic acid would be consumed there and less hydrogen gas would be generated. This task involves literature survey of technologies to perform the nitrate to hydroxide conversion, selection of the most promising technologies, preparation of a flowsheet and design of a system. The most promising technologies are electrochemical reduction of nitrates and chemical reduction with hydrogen or ammonia. The primary reviewed technologies are listed and they aredescribed in more detail later in the report: (1) Electrochemical destruction; (2) Chemical reduction with agents such as ammonia, hydrazine or hydrogen; (3) Hydrothermal reduction process; and (4) Calcination. Only three of the technologies on the list have been demonstrated to generate usable amounts of caustic; electrochemical reduction and chemical reduction with ammonia, hydrazine or hydrogen and hydrothermal reduction. Chemical reduction with an organic reactant such as formic acid generates carbon dioxide which reacts with caustic and is thus counterproductive. Treatment of nitrate with aluminum or other active metals generates a solid product. High temperature calcination has the potential to generate sodium oxide which may be hydrated to sodium hydroxide, but this is unproven. The following criteria were developed to evaluate the most suitable option. The numbers in brackets after the criteria are relative weighting factors to account for importance: (1) Personnel exposure to radiation for installation, routine operation and maintenance; (2) Non-radioactive safety issues; (3) Whether the technology generates caustic and how many moles of caustic are generated per mole of nitrate plus nitrite decomposed; (4) Whether the technology can handle nitrate and nitrite at the concentrations encountered in waste; (5) Maturity of technology; (6) Estimated annual cost of operation (labor, depreciation, materials, utilities); (7) Capital cost; (8) Selectivity to nitrogen as decomposition product (other products are flammable and/or toxic); (9) Impact of introduced species; (10) Selectivity for destruction of nitrate vs. nitrite; and (11) Cost of deactivation and demolition. Each technology was given a score from one

Steimke, J.

2011-02-01T23:59:59.000Z

113

Enediolate-Dilithium Amide Mixed Aggregates in the Enantioselective Alkylation of Arylacetic Acids: Structural  

E-Print Network (OSTI)

Despite remarkable progress in the field of catalytic asymmetric synthesis,1 asymmetric alkylations of lithium enolates are pre- dominantly based on covalent chiral auxiliaries even in the simplest functionalizations.2-5 Recently, we developed an alkylation of the dianions of aryl and heteroaryl acetic acids6

Collum, David B.

114

A Practical and Highly Stereoselective Umpolung Alternative to the Alkylation of Chiral Enolates  

E-Print Network (OSTI)

-chiral center of high optical purity based on the SN2 displace- ment reaction of alkyl cuprates on chiral allyl, the reaction sometimes leads to self-condensa- tion byproducts. The Lewis acid induced alkylation of silyl enol ethers allows reaction with SN1-prone electrophiles but is of limited use with ester or amide derived O

Spino, Claude

115

Molten nitrate salt technology development status report  

SciTech Connect

Recognizing thermal energy storage as potentially critical to the successful commercialization of solar thermal power systems, the Department of Energy (DOE) has established a comprehensive and aggressive thermal energy storage technology development program. Of the fluids proposed for heat transfer and energy storage molten nitrate salts offer significant economic advantages. The nitrate salt of most interest is a binary mixture of NaNO/sub 3/ and KNO/sub 3/. Although nitrate/nitrite mixtures have been used for decades as heat transfer and heat treatment fluids the use has been at temperatures of about 450/sup 0/C and lower. In solar thermal power systems the salts will experience a temperature range of 350 to 600/sup 0/C. Because central receiver applications place more rigorous demands and higher temperatures on nitrate salts a comprehensive experimental program has been developed to examine what effects, if any, the new demands and temperatures have on the salts. The experiments include corrosion testing, environmental cracking of containment materials, and determinations of physical properties and decomposition mechanisms. This report details the work done at Sandia National Laboratories in each area listed. In addition, summaries of the experimental programs at Oak Ridge National Laboratory, the University of New York, EIC Laboratories, Inc., and the Norwegian Institute of Technology on molten nitrate salts are given. Also discussed is how the experimental programs will influence the near-term central receiver programs such as utility repowering/industrial retrofit and cogeneration. The report is designed to provide easy access to the latest information and data on molten NaNO/sub 3//KNO/sub 3/ for the designers and engineers of future central receiver projects.

Carling, R.W.; Kramer, C.M.; Bradshaw, R.W.; Nissen, D.A.; Goods, S.H.; Mar, R.W.; Munford, J.W.; Karnowsky, M.M.; Biefeld, R.N.; Norem, N.J.

1981-03-01T23:59:59.000Z

116

Extraction of nitric acid, uranyl nitrate, and bismuth nitrate from aqueous nitric acid solutions with CMPO  

SciTech Connect

DOE sponsored development of the transuranium extraction (TRUEX) process for removing actinides from radioactive wastes. The solvent is a mixture of CMPO and TBP. Since the extraction characteristics of CMPO are not as well understood as those of TBP, the extraction of nitric acid, uranyl nitrate, and bismuth nitrate with CMPO (dissolved in n-dodecane) were studied. Results indicate that CMPO extracts nitric acid with a 1:1 stoichiometry; equilibrium constant is 2. 660{plus_minus}0.092 at 25 C, and extraction enthalpy is -5. 46{plus_minus}0.46 kcal/mol. Slope analysis indicates that uranyl nitrate extracts with a mixed equilibria of 1:1 and 2:1 stoichiometries in nearly equal proportion. Equil. constant of the 2: 1 extraction was 1.213 {times} 10{sup 6}{plus_minus}3.56 {times} 10{sup 4} at 25 C; reaction enthalpy was -9.610{plus_minus}0.594 kcal/mol. Nitration complexation constant is 8.412{plus_minus}0.579, with an enthalpy of -10.72{plus_minus}1.87 kcal/mol. Bismuth nitrate also extracts with a mixed equilibria of (perhaps) 1:1 and 2:1 stoichiometries. A 2:1 extraction equilibrium and a nitrate complexation adequately model the data. Kinetics and enthalpies were also measured.

Spencer, B.B.

1995-08-01T23:59:59.000Z

117

Volatile liquid hydrocarbon characterization of underwater hydrocarbon vents and formation waters from offshore production operations  

Science Journals Connector (OSTI)

Volatile liquid hydrocarbon characterization of underwater hydrocarbon vents and formation waters from offshore production operations ... The environmental implications of offshore oil and gas activities ... The environmental implications of offshore oil and gas activities ...

Theodor C. Sauer

1981-08-01T23:59:59.000Z

118

HYDROCARBON AND SULFUR SENSORS FOR SOFC SYSTEMS  

SciTech Connect

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

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

2003-11-01T23:59:59.000Z

119

Hydrocarbon Separations in Metal–Organic Frameworks  

Science Journals Connector (OSTI)

Given the large differences in the physical properties of methane and C2 hydrocarbons, both size selective effects and metal–hydrocarbon interactions can be tuned to achieve a high selectivity within a metal–organic framework. ... Polycyclic aromatic hydrocarbons, or PAHs, are carcinogenic byproducts of incomplete combustion of organic matter such as fossil fuels. ... data and the heats of adsorption were found to fit well to a small group of mol. ...

Zoey R. Herm; Eric D. Bloch; Jeffrey R. Long

2013-11-22T23:59:59.000Z

120

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

Note: This page contains sample records for the topic "hydrocarbons alkyl nitrates" 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

catalytic_upgrading_sugars_to_hydrocarbons  

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

phase reforming into hydrocarbons for fuels and co-product commodities. Process Block Diagram Next Steps Additional modeling is necessary to quantify baseline costs associated...

122

Application of advanced hydrocarbon characterization and its...  

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

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

123

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

124

Biodegradation of Aromatic Hydrocarbons in an Extremely Acidic Environment  

Science Journals Connector (OSTI)

...biodegradation of aromatic hydrocarbons can occur in environments...Polycyclic aromatic hydrocarbons (PAHs) occur as common...formed by incomplete combustion of fossil fuels...enrichments with aromatic hydrocarbons, mineralization assays...lysis was initiated by heat and sodium dodecyl...

Raymond D. Stapleton; Dwayne C. Savage; Gary S. Sayler; Gary Stacey

1998-11-01T23:59:59.000Z

125

High Levels of Carcinogenic Polycyclic Aromatic Hydrocarbons in Mate Drinks  

Science Journals Connector (OSTI)

...polycyclic aromatic hydrocarbons| Introduction Esophageal...polycyclic aromatic hydrocarbon (PAH) content. PAHs...usually exposed to combustion products from burning...SRM 2260a Aromatic Hydrocarbons in Toluene, SRM 2269...dichloromethane; heat: preheat cell at 100C...

Farin Kamangar; Michele M. Schantz; Christian C. Abnet; Renato B. Fagundes; and Sanford M. Dawsey

2008-05-01T23:59:59.000Z

126

High Levels of Carcinogenic Polycyclic Aromatic Hydrocarbons in Mate Drinks  

Science Journals Connector (OSTI)

...polycyclic aromatic hydrocarbons (PAH), including...polycyclic aromatic hydrocarbons| Introduction...mechanism. However, data on the association...polycyclic aromatic hydrocarbon (PAH) content...usually exposed to combustion products from burning...dichloromethane; heat: preheat cell...

Farin Kamangar; Michele M. Schantz; Christian C. Abnet; Renato B. Fagundes; and Sanford M. Dawsey

2008-05-01T23:59:59.000Z

127

MICROCHEMICALJOURNAL39, 160-165Hydrocarbons in Air  

E-Print Network (OSTI)

from Waters Associates. Water used was deionized, distilled, and hydrocarbon filtered (BarnsteadMICROCHEMICALJOURNAL39, 160-165Hydrocarbons in Air to extract polycyclic aromatic hydrocarbons (PAH) from air particulate sampleswas investigated. High

Canberra, University of

128

Metabolism of Polycyclic Aromatic Hydrocarbons in Cell Cultures  

Science Journals Connector (OSTI)

...metabolism of polycyclic aromatic hydrocarbons to water-soluble and organic-soluble...metabolism of polycyclic aromatic hydrocarbons to water-soluble and organic-soluble...cytotoxicity and conversion of hydrocarbons to water-soluble products (Chart...

Eliezer Huberman; James K. Selkirk; and Charles Heidelberger

1971-12-01T23:59:59.000Z

129

High Levels of Carcinogenic Polycyclic Aromatic Hydrocarbons in Mate Drinks  

Science Journals Connector (OSTI)

...polycyclic aromatic hydrocarbons (PAH), including...80C) or cold (5C) water. Measurements were...polycyclic aromatic hydrocarbons in mate drinks. | Drinking...polycyclic aromatic hydrocarbons (PAH), including...cold (5 degrees C) water. Measurements were...

Farin Kamangar; Michele M. Schantz; Christian C. Abnet; Renato B. Fagundes; and Sanford M. Dawsey

2008-05-01T23:59:59.000Z

130

Hydrocarbons in rift basins: the role of stratigraphy  

Science Journals Connector (OSTI)

...versus shallow-water environments...A (1999) Hydrocarbons in rift basins...Facies and hydrocarbon potential The...availability of water. This can either...form seals for hydrocarbons. The shallow-water environ- ments...

1999-01-01T23:59:59.000Z

131

Learning and discrimination of cuticular hydrocarbons in a social insect  

Science Journals Connector (OSTI)

...colony members. Cuticular hydrocarbons (CHCs) play a central...CHC profile with synthetic hydrocarbons [4-6] reveal that some hydrocarbons elicit aggression. However...non-volatile, insoluble in water and therefore difficult...

2012-01-01T23:59:59.000Z

132

Tensile Effective Stresses in Hydrocarbon Storage Caverns  

E-Print Network (OSTI)

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

Paris-Sud XI, Université de

133

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

134

The Effects of Two Isomeric Benzoflavones on Aryl Hydrocarbon Hydroxylase and the Toxicity and Carcinogenicity of Polycyclic Hydrocarbons  

Science Journals Connector (OSTI)

...recrystallized from alcohol : water. For tissue culture experiments the hydrocarbons and benzoflavones...metabolism of the hydrocarbons to water-soluble derivatives...chloroform:methanol. Hydrocarbon-3 H metabolized to water-soluble derivatives...

Leila Diamond; Rosemary McFall; Joel Miller; and Harry V. Gelboin

1972-04-01T23:59:59.000Z

135

Hydrocarbon fouling of SCR during Premixed Charge Compression...  

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

Hydrocarbon fouling of SCR during Premixed Charge Compression Ignition (PCCI) combustion Hydrocarbon fouling of SCR during Premixed Charge Compression Ignition (PCCI) combustion...

136

Algal Lipid Extraction and Upgrading to Hydrocarbons Technology...  

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

and upgrading pathway to be competitive with petroleum-derived gasoline-, diesel-, and jet-range hydrocarbon blendstocks. Algal Lipid Extraction and Upgrading to Hydrocarbons...

137

DOE Perspectives on Advanced Hydrocarbon-based Biofuels | Department...  

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

DOE Perspectives on Advanced Hydrocarbon-based Biofuels DOE Perspectives on Advanced Hydrocarbon-based Biofuels Zia Haq, DPA Coordinator, presentation on DOE Perspectives on...

138

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

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

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

139

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

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

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

140

Palladium-catalyzed allylic alkylation via decarboxylative and retro-Claisen C-C cleavage methods  

E-Print Network (OSTI)

Presented herein is the development of new methods for Pd-catalyzed allylic alkylation with a central focus on reactions that generate molecular complexity rapidly with little waste byproduct. With this simply stated, yet ...

Grenning, Alexander James

2012-05-31T23:59:59.000Z

Note: This page contains sample records for the topic "hydrocarbons alkyl nitrates" 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

Degradable Terpolymers with Alkyl Side Chains Demonstrate Enhanced Gene Delivery Potency and Nanoparticle Stability  

E-Print Network (OSTI)

Degradable, cationic poly(?-amino ester)s (PBAEs) with alkyl side chains are developed for non-viral gene delivery. Nanoparticles formed from these PBAE terpolymers exhibit significantly enhanced DNA transfection potency ...

Eltoukhy, Ahmed A.

142

E-Print Network 3.0 - alkylation response protein Sample Search...  

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

Summary: -DNA methyltransferases such as Ada and Ogt in E. coli and MGMT (or AGT) in humans. These proteins directly remove alkyl... purified proteins have been reported only for...

143

E-Print Network 3.0 - alkylating agent monobromobimane Sample...  

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

Naphthoate and Central Amide in Sequence-Dependent Summary: . In these assays, a 100-fold excess of agents was used in order to provide measurable alkylation yields in single......

144

1208 Organometallics1988,7,1208-1213 Copper(I) Alkyls. Synthesis and Characterization of Tertiary  

E-Print Network (OSTI)

-Champaign, Urbana, Illinois 61801 Received December 28. 1986 Alkylation of copper(I1)acetate reflections and 62 variables. Introduction Lithium dialkylcuprates, LiCuR2,are used extensively in organic

Girolami, Gregory S.

145

E-Print Network 3.0 - alkyl methyl ketones Sample Search Results  

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

l S e m e s t e r 1 9 9 7 Summary: . These acetylides are nucleophilic enough to undergo SN2 reactions with alkyl halides. There are two steps involved... : (a) formation of the...

146

Preparation of synthetic hydrocarbon lubricants  

SciTech Connect

A process is described for preparing synthetic lubricating materials which process comprises: (a) reacting (i) at least a portion of a reaction product of the liquid phase oligomerization of propylene, butylene or mixtures thereof containing a C/sub 6/ olefin component, (ii) a linear olefin reactant having an average carbon number ranging from about 10 to about 18 in the presence of a catalyst, (b) separating from the reaction mixture of (a) hydrocarbons which distill at a temperature above about 660/sup 0/ F. (316/sup 0/ C.), and (c) hydrogenating the reaction product of (b) by contact with hydrogen with or without a catalyst at a temperature ranging from about 25/sup 0/ C. to about 300/sup 0/ C.

Johnson, T.H.

1986-10-07T23:59:59.000Z

147

Electrophilic Metal Alkyl Chemistry in New Ligand Environments  

SciTech Connect

The goals of this project were to design new electrophilic metal alkyl complexes and to exploit these systems in fundamental studies of olefin polymerization and other important and new catalytic reactions. A key target reaction is insertion copolymerization of olefins and polar CH2=CHX vinyl monomers such as vinyl halides and vinyl ethers. During the period covered by this report we (i) investigated the properties of ortho-alkoxy-arylphosphine ligands in Ni-based olefin polymerization catalysts, (ii) studied the synthesis of double-end-capped polyethylene using group 4 metal catalysts that contain tris-pyrazolylborate ligands, (iii) explored the ethylene insertion reactivity of group 4 metal tris-pyrazolyl-borate complexes, (iv) showed that (?-diimine)PdMe{sup +} species undergo multiple insertion of silyl vinyl ethers, (v) synthesized and explored the reactivity of base-free Ni benzyl complexes that contain ortho-phosphino-arene sulfonate ligands, (vi) established the mechanism of the reaction of vinyl chloride with (?-diimine)PdMe{sup +} catalysts, (vii) explored the role of cationic polymerization and insertion chemistry in the reactions of vinyl ethers with (?-diimine)PdMe{sup +} species, (viii) discovered a new class of self-assembled tetranuclear Pd catalysts that produce high molecular weight linear polyethylene and copolymerize ethylene and vinyl fluoride, and (ix) developed model systems that enabled investigation of cis-trans isomerization of {phosphine-sulfonate}Pd(II) complexes.

Jordan, Richard F. [University of Chicago] University of Chicago

2013-06-30T23:59:59.000Z

148

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

149

Cross-Couplings of Unactivated Secondary Alkyl Halides: Room-Temperature Nickel-Catalyzed Negishi Reactions of Alkyl Bromides and Iodides  

E-Print Network (OSTI)

-carbon bonds.1 To date, most studies of these processes have focused on forming Csp2-Csp2 (particularly biaryl-coupling catalysts for generating Csp3-Csp3 bonds.2 The availability of general methods for building the latter set to constructing Csp3-Csp3 bonds via metal- catalyzed cross-couplings of alkyl electrophiles with alkylmetals

Fu, Gregory C.

150

Analyzing Biomass Conversion into Liquid Hydrocarbons  

Science Journals Connector (OSTI)

Variants of the Fischer–Tropsch producer-gas conversion into liquid hydrocarbons are analyzed under the ... is attained in the reactions occurring in the biomass gasification. When the raw material is wood ... th...

V. D. Meshcheryakov; V. A. Kirillov

2002-09-01T23:59:59.000Z

151

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...

Kanga, Shahrukh

2012-06-07T23:59:59.000Z

152

E-Print Network 3.0 - ammonium compounds n-alkyl Sample Search...  

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

which are incompatible with other compounds. Summary: compounds, fulminic acid Sodium carbon tetrachloride, carbon dioxide, water Sodium nitrite ammonium nitrate... chemicals...

153

Nitrate-Cancrinite Precipitation on Quartz Sand in Simulated Hanford  

E-Print Network (OSTI)

Nitrate-Cancrinite Precipitation on Quartz Sand in Simulated Hanford Tank Solutions B A R R Y R . B minerals at the U.S. Department of Energy's Hanford site in Washington. Nitrate-cancrinite began's (DOE) Hanford Site in southeast Washington since the late 1950s (1). To predict the fate

Illinois at Chicago, University of

154

Phytoplankton biomass and residual nitrate in the pelagic ecosystem  

Science Journals Connector (OSTI)

...research-article Research Article Phytoplankton biomass and residual nitrate in the pelagic ecosystem...are linked to changes in the chlorophyll biomass. The model can be treated analytically...Mathematical bounds are found for the autotrophic biomass and the residual nitrate in terms of the...

2003-01-01T23:59:59.000Z

155

CU(II): catalyzed hydrazine reduction of ferric nitrate  

SciTech Connect

A method is described for producing ferrous nitrate solutions by the cupric ion-catalyzed reduction of ferric nitrate with hydrazine. The reaction is complete in about 1.5 hours at 40/sup 0/C. Hydrazoic acid is also produced in substantial quantities as a reaction byproduct.

Karraker, D.G.

1981-11-01T23:59:59.000Z

156

Evaluation of nitrate and nitrite destruction/separation technologies  

SciTech Connect

This report describes and evaluates four types of nitrate and nitrite destruction and separation technologies that could be used to treat the aqueous, alkaline, nitrate-bearing mixed waste that is generated by the In-Tank Precipitation (ITP) process at the Savannah River Site (SRS). The technologies considered in this report include thermal, hydrothermal, chemical, and electrochemical technologies.

Hobbs, D.T.

1997-08-29T23:59:59.000Z

157

Methanol conversion to higher hydrocarbons  

SciTech Connect

Several indirect options exist for producing chemicals and transportation fuels from coal, natural gas, or biomass. All involve an initial conversion step to synthesis gas (CO and H{sub 2}). Presently, there are two commercial technologies for converting syngas to liquids: Fischer-Tropsch, which yields a range of aliphatic hydrocarbons with molecular weights determined by Schulz-Flory kinetics, and methanol synthesis. Mobil`s diversity of technology for methanol conversion gives the methanol synthesis route flexibility for production of either gasoline, distillate or chemicals. Mobil`s ZSM-5 catalyst is the key in several processes for producing chemicals and transportation fuels from methanol: MTO for light olefins, MTG for gasoline, MOGD for distillates. The MTG process has been commercialized in New Zealand since 1985, producing one-third of the country`s gasoline supply, while MTO and MOGD have been developed and demonstrated at greater than 100 BPD scale. This paper will discuss recent work in understanding methanol conversion chemistry and the various options for its use.

Tabak, S.A. [Mobil Research and Development Corp., Princeton, NJ (United States). Central Research Lab.

1994-12-31T23:59:59.000Z

158

Thermal Decomposition of Nitrated Tributyl Phosphate  

SciTech Connect

Contact between tributyl phosphate and aqueous solutions of nitric acid and/or heavy metal nitrate salts at elevated temperatures can lead to exothermic reactions of explosive violence. Even though such operations have been routinely performed safely for decades as an intrinsic part of the Purex separation processes, several so-called ``red oil`` explosions are known to have occurred in the United States, Canada, and the former Soviet Union. The most recent red oil explosion occurred at the Tomsk-7 separations facility in Siberia, in April 1993. That explosion destroyed part of the unreinforced masonry walls of the canyon-type building in which the process was housed, and allowed the release of a significant quantity of radioactive material.

Paddleford, D.F. [Westinghouse Savannah River Company, Aiken, SC (United States); Hou, Y.; Barefield, E.K.; Tedder, D.W.; Abdel-Khalik, S.I. [Georgia Institute of Technology, GA (United States)

1995-01-01T23:59:59.000Z

159

Thermal decomposition of nitrated tributyl phosphate  

SciTech Connect

Extended contact between heated mixtures of tri-n-butyl phosphate (TBP) and aqueous solutions of nitric acid and/or heavy metal nitrate salts at elevated temperatures can lead to exothermic reactions of explosive violence. Most solvent extraction operations are conducted at ambient conditions without heating TBP and have been performed safely for decades, but several explosions involving TBP have occurred in the US, Canada, and the former Soviet Union. This investigation was undertaken to characterize the products of thermal decomposition of both single- and two-phase mixtures of TBP, nitric acid, and water under a variety of conditions. The data indicate that the extent of reaction and the rate of gaseous product formation are affected by the presence of Zr{sup 4+}, distillation compared with reflux conditions, temperature, water/HNO{sub 3} and HNO{sub 3}/TBP ratios, and whether the decomposition occurs under constant pressure or constant volume conditions. Higher reaction temperatures accelerate the rate of decomposition, but the extent of decomposition, as measured by the quantity of gaseous products, was greater at lower temperatures when the decomposition was performed under distillation conditions. Higher gas production occurs under reflux conditions, lower H{sub 2}O/HNO{sub 3} ratios, and when a separate water-HNO{sub 3} phase is initially present. The major gaseous products include N{sub 2}, CO, CO{sub 2}, NO, and N{sub 2}O. Measurable amounts of NO{sub 2} were not present in the final product mixture, although an orange color suggesting the presence of NO{sub 2} was observed in the early stages of decomposition. The major liquid products were dibutyl phosphoric acid, butyl nitrate, and water. Small amounts of C{sub 1}-C{sub 4} carboxylic acids were also present. Because of the small sample sizes that were employed and the isothermal conditions of the decomposition, runaway reactions were not observed. Some possible reaction pathways are considered.

Hou, Y.; Barefield, E.K.; Tedder, D.W.; Abdel-Khalik, S.I. [Georgia Inst. of Technology, Atlanta, GA (United States)

1996-03-01T23:59:59.000Z

160

Chlorofluorocarbons  

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

Atmospheric Trace Gases » Chlorofluorocarbons Atmospheric Trace Gases » Chlorofluorocarbons Chlorofluorocarbons CFC-11 (trichlorofluoromethane - CFCl2) Advanced Global Atmospheric Gases Experiment (AGAGE, Prinn et al.) Methane, Nonmethane Hydrocarbons, Alkyl Nitrates, and Chlorinated Carbon Compounds including 3 Chlorofluorocarbons (CFC-11, CFC-12, and CFC-113) in Whole-air Samples (Blake) Globally Averaged Atmospheric CFC-11 Concentrations: Monthly and Annual Data for the Period 1975-1992 (Khalil and Rasmussen) Atmospheric CFC, CCl4, and SF6 Historical Update (Bullister) CFC-12 (dichlorodifluoromethane - CF2Cl2) Advanced Global Atmospheric Gases Experiment (AGAGE, Prinn et al.) Methane, Nonmethane Hydrocarbons, Alkyl Nitrates, and Chlorinated Carbon Compounds including 3 Chlorofluorocarbons (CFC-11, CFC-12, and

Note: This page contains sample records for the topic "hydrocarbons alkyl nitrates" 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

Polyhalogenated hydrocarbon refrigerants and refrigerant oils colored with fluorescent dyes and method for their use as leak detectors  

SciTech Connect

A leak detectable refrigeration composition is described comprising: (A) a refrigeration liquid selection from the group consisting of: (1) a polyhalogenated hydrocarbon refrigerant; (2) a refrigeration oil selected from the group consisting of naphthenic oils, paraffinic oils, alkylated benzenes, silicones, polyglycols, diesters or triesters of dicarboxylic or tricarboxylic acids, and polyalkyl silicate oils, and (3) a mixture of A(1) and A(2), and (B) a fluorescent dye compound or composition comprising the dye selected from the group consisting of: (1) a fluorescent dye selected from the group consisting of perylene, naphthoxanthene, monocyclic aromatic compounds having an organometallic compound, (2) a solution of fluorescent dye in a solvent, and (3) a mixture of B(1) and B(2). The fluorescent dye compound or composition is soluble in the refrigeration liquid. The concentration of the dye being at least 0.001 grams per 100 grams of the refrigeration liquid.

Parekh, M.

1988-07-19T23:59:59.000Z

162

Dose-dependent cytotoxic and mutagenic effects of antineoplastic alkylating agents on human lymphoblastoid cells  

SciTech Connect

The alkylating agents in clinical use as antineoplastics are strongly implicated as human carcinogens on the basis of animal studies and human epidemiologic studies. However, there is little quantitative information on the extent to which exposure to these drugs is mutagenic for normal (non-malignant) cells and the extent to which such mutagenicity correlates with cytotoxicity of these agents. Human lymphoblastoid cells (WIL2-NS) were exposed to graded doses of eight antineoplastic alkylating agents. Dose-dependent decreases in survival were used to calculate IC{sub 50}s for each of the drugs tested. The mutagenicity of these agents is correlated strongly with cytotoxicity. These results quantitate the dose-dependent cytotoxic and mutagenic effects of these bifunctional alkylating agents on human cells. All are cytotoxic and mutagenic, although their mutagenic efficiency varies.

Sanderson, B.J.S.; Johnson, K.J.; Henner, W.D. (Oregon Health Sciences Univ., Portland (United States))

1991-01-01T23:59:59.000Z

163

Groundwater nitrates in the Seymour Aquifer: problem or resource?  

E-Print Network (OSTI)

24 tx H2O Fall 2012 Story by Alejandra Arreola-Triana In the Rolling Plains of Texas, the Seymour Aquifer is the major source of water for Haskell, Jones and Knox counties. #31;e water from the Seymour Aquifer, however, contains nitrate levels... are working on ways to manage the nitrate levels in this aquifer. Tracking the source Nitrates in groundwater can come from runo#27;, fertilizer use, leaks from septic tanks, sewage and erosion of natural deposits, according to the U.S. Environmental...

Arreola-Triana, Alejandra

2012-01-01T23:59:59.000Z

164

Effect of Polyethylene Glycol, Alkyl, and Oligonucleotide Spacers on the Binding, Secondary Structure, and Self-Assembly of Fractalkine  

E-Print Network (OSTI)

Effect of Polyethylene Glycol, Alkyl, and Oligonucleotide Spacers on the Binding, Secondary-amphiphiles with no spacer (NoSPR), polyethylene glycol (PEG4, PEG8, PEG24), alkyl (C12 and C24), or oligonucleotide (T10 a polyethylene glycol (PEG) or an oligo-T (thymine) spacer is added to the aptamer, especially when attaching

Kokkoli, Efie

165

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":""}]}

166

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

167

Using supercritical fluids to refine hydrocarbons  

DOE Patents (OSTI)

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

Yarbro, Stephen Lee

2014-11-25T23:59:59.000Z

168

Thermal decomposition of nitrated tributyl phosphate  

SciTech Connect

Tri-n-butyl phosphate (TBP), nitric acid and water mixtures are subject to thermal decomposition. The gaseous and liquid decomposition product yields are highly path dependent. Higher temperatures accelerate decomposition rates, but may result in lower extent of reaction than comparable low temperature cases. Actual extent of reaction, and gaseous by-products generation, are affected by the presence of Zr(IV), condensate reflux back into the reaction vessel, the water/HNO{sub 3} and the HNO{sub 3}/TBP molar ratios, and whether the decomposition occurs at isobaric or constant volume conditions. Higher gaseous production results from condensate reflux, lower H{sub 2}O/HNO{sub 3} ratios, and with excess HNO{sub 3} and water present as a second liquid phase. Principal gaseous products include N{sub 2}, CO, CO{sub 2}, NO and N{sub 2}O. Measurable concentrations of NO{sub 2} were not observed, although gas coloration indicative of NO{sub 2} were obsessed during the beginning of decomposition measurements. Principal liquid products are dibutyl phosphoric acid and butyl nitrate. Air sparging of TBP solutions (e.g., thru transfers using air lift pumps) may increase the hazards of TBP decomposition reactions by lowering the H{sub 2}O/HNO{sub 3} molar ratios. Runaway reactions were not observed under the conditions of this study. Possible reaction mechanisms and pathways are discussed.

Hou, Y.; Barefield, E.K.; Tedder, D.W.; Abdel-Khalik, S.I. [Georgia Institute of Technology, Atlanta, GA (United States)

1995-12-31T23:59:59.000Z

169

Weapon Systems Using Samine, Melanj and Isopropyl Nitrate  

Science Journals Connector (OSTI)

This paper describes the uses and properties of three chemicals stored in Azerbaijan: melanj, samine, and isopropyl nitrate. These three chemicals have historically been used in the manufacturing of liquid bal...

Vugar Gafarov

2005-01-01T23:59:59.000Z

170

Project Profile: Advanced Nitrate Salt Central Receiver Power Plant  

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

Abengoa, under the Baseload CSP FOA, will demonstrate a 100-megawatt electrical (MWe) central receiver plant using nitrate salt as the receiver coolant, thermal storage medium, and heat transport fluid in the steam generator.

171

NITRATE REMOVAL BY CALCINED HYDROTALCITE-TYPE COMPOUNDS  

Science Journals Connector (OSTI)

...contaminant in drinking water (which is primarily...levels in contaminated waters. Reverse osmosis, ion exchange, and electrodialysis are considered the best...nitrate-contaminated water (Canter, 1997; Haugen...solid interface. Treatment processes, such as...

María M. Socías-Viciana; María D. Ureña-Amate; Emilio González-Pradas; María J. García-Cortés; Cristina López-Teruel

172

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

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

various hydrocarbons on monolithic hydrocarbon adsorber Dae Jung Kim,a Ji Man Kim,a Jae Eui Yie... and conversion of various hydrocarbons on monolithic hydrocarbon adsorbers were...

173

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

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

various hydrocarbons on monolithic hydrocarbon adsorber Dae Jung Kim,a Ji Man Kim,a Jae Eui Yie... and conversion of various hydrocarbons on monolithic hydrocarbon adsorbers were...

174

Sexual selection on cuticular hydrocarbons of male sagebrush crickets in the wild  

Science Journals Connector (OSTI)

...association between cuticular hydrocarbon composition and desiccation...temperature on cuticular lipids and water balance in a desert Drosophila...interactions for cuticular hydrocarbon expression in Drosophila simulans...evolutionary roles of cuticular hydrocarbons in Diptera. In Insect hydrocarbons...

2013-01-01T23:59:59.000Z

175

Sustainable treatment of hydrocarbon-contaminated industrial land   

E-Print Network (OSTI)

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

Cunningham, Colin John

2012-06-25T23:59:59.000Z

176

Chapter 9 - Chemical and Physical Properties of Hydrocarbons  

Science Journals Connector (OSTI)

Publisher Summary Hydrocarbons are the simplest organic compounds and contain only carbon and hydrogen but they can be straight chain or branched chain with the same empirical formula but showing differences in properties. Chemical change results in the hydrocarbon yielding a product that may be entirely different in composition to the starting hydrocarbon—the exception is the isomerization reaction where a straight-chain hydrocarbon is converted to a branched-chain hydrocarbon. Chemical properties of hydrocarbons describe the potential of hydrocarbons to undergo chemical change or reaction by virtue of the hydrocarbon structure. Physical properties can be observed or measured without changing the composition of matter. Physical properties are used to observe and describe matter. Physical properties that are of interest in the current context include: boiling point, melting point, density, vapor density, flash point, ignition temperature, and dew point.

James G. Speight

2011-01-01T23:59:59.000Z

177

FORMATION OF CARBON-CARBON BONDS IN THE PHOTOCHEMICAL ALKYLATION OF POLYCYCLIC AROMATIC  

E-Print Network (OSTI)

HYDROCARBONS TANIA B. MAHAJAN1, JAMIE E. ELSILA1, DAVID W. DEAMER2 and RICHARD N. ZARE1 1 Department July 2002) Abstract. The reaction of polycyclic aromatic hydrocarbons (PAHs) with alkanes was examined films in contact with simulated ocean water, and in matrices simulating ISM conditions. Photoalkylation

Zare, Richard N.

178

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

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

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

179

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

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

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

180

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

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

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

Note: This page contains sample records for the topic "hydrocarbons alkyl nitrates" 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

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

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

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

182

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

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

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

183

E-Print Network 3.0 - aromatic hydrocarbons Sample Search Results  

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

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

184

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

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

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

185

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

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

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

186

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

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

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

187

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

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

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

188

Biodegradation of monoaromatic hydrocarbons by aquifer microorganisms using oxygen, nitrate, or nitrous oxide as the terminal electron acceptor.  

Science Journals Connector (OSTI)

...I. Mayfield. 1986. Remediation of gasoline-contaminated...Aerobic denitrification as an innovative method for in-situ biological remediation of contaminated sub- surface...underground storage tanks: remediation with emphasis on in situ...

S R Hutchins

1991-08-01T23:59:59.000Z

189

Biological Conversion of Sugars to Hydrocarbons Technology Pathway  

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

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

190

THE ELECTRON MICROSCOPY OF HYDROCARBON PRODUCTION IN PARTHENIUM ARGENTATUM (GUAYULE)  

E-Print Network (OSTI)

conversion of solar energy is the production of hydrocarbonsproduction of hydrocarbons. Mankind's use of biologically converted solar energy

Bauer, T.E.

2010-01-01T23:59:59.000Z

191

aromatic hydrocarbons coated: Topics by E-print Network  

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

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

192

Serendipitous alkylation of a Plk1 ligand uncovers a new binding channel  

E-Print Network (OSTI)

We obtained unanticipated synthetic byproducts from alkylation of the ?[superscript 1] nitrogen (N3) of the histidine imidazole ring of the polo-like kinase-1 (Plk1) polo-box domain (PBD)-binding peptide PLHSpT. For the ...

Lim, Dan

193

Oligonucleoside alkyl or arylphosphonate derivatives capable of crosslinking with or cleaving nucleic acids  

DOE Patents (OSTI)

A composition for inactivating a target nucleic acid which comprises an oligonucleoside alkyl or arylphosphonate analogue which is complementary to the sequence of the target nucleic acid is provided. It includes a functional group which reacts with the target nucleic acid to render the target nucleic acid inactive or nonfunctional. 16 figs.

Miller, P.S.; Ts'o, P.O.P.

1999-06-15T23:59:59.000Z

194

Whitesides et al. f Reaction ctfAlkyl Halides with Magnesiunt Mechanismof Formationof GrignardReagents.  

E-Print Network (OSTI)

carbanionsand carbonium ionsare not intermediates,and tliat the transition-itut. structuredoesnot resemblean SN2.rnagncsiumatom at the mctal surface(or possibly in solution) rrrrghtdisplacehelidefrotncarbonin an SN2-likc rcuctionor inrcrlWhitesides et al. f Reaction ctfAlkyl Halides with Magnesiunt Mechanismof Formationof Grignard

Prentiss, Mara

195

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

196

Molecular carbon isotopic evidence for the origin of geothermal hydrocarbons  

Science Journals Connector (OSTI)

... in the flask's headspace. This procedure produced negligible amounts of contaminating hydrocarbons. The geothermal hydrocarbons were separated and combusted, and the carbon dioxide product purified and measured using ... of the pyrolysis and spark discharge experiments, b, Isotopic abundance of hydrocarbons from four geothermal localities as follows: D, Cerro Prieto, well M-5, sampled January 1979; ...

David J. Des Marais; Jason H. Donchin; Nancy L. Nehring; Alfred H. Truesdell

1981-08-27T23:59:59.000Z

197

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

198

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

199

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

200

Nonlinear dependence of the solubility of water in hydrocarbons on the molar volume of the hydrocarbon  

Science Journals Connector (OSTI)

The solubility of water in fifty hydrocarbon solvents at 20°C is estimated by ... in nonspecific cohesion forces, and assuming that water is primarily monomeric in solution, the prediction ... breaking of the H-b...

Paul Ruelle; Ulrich W. Kesselring

1996-07-01T23:59:59.000Z

Note: This page contains sample records for the topic "hydrocarbons alkyl nitrates" 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

Mass Transfer of Polynuclear Aromatic Hydrocarbons from  

E-Print Network (OSTI)

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

Peters, Catherine A.

202

Interaction and dynamics of (alkylamide + electrolyte) deep eutectics: Dependence on alkyl chain-length, temperature, and anion identity  

SciTech Connect

Here we investigate the solute-medium interaction and solute-centered dynamics in (RCONH{sub 2} + LiX) deep eutectics (DEs) via carrying out time-resolved fluorescence measurements and all-atom molecular dynamics simulations at various temperatures. Alkylamides (RCONH{sub 2}) considered are acetamide (CH{sub 3}CONH{sub 2}), propionamide (CH{sub 3}CH{sub 2}CONH{sub 2}), and butyramide (CH{sub 3}CH{sub 2}CH{sub 2}CONH{sub 2}); the electrolytes (LiX) are lithium perchlorate (LiClO{sub 4}), lithium bromide (LiBr), and lithium nitrate (LiNO{sub 3}). Differential scanning calorimetric measurements reveal glass transition temperatures (T{sub g}) of these DEs are ?195 K and show a very weak dependence on alkyl chain-length and electrolyte identity. Time-resolved and steady state fluorescence measurements with these DEs have been carried out at six-to-nine different temperatures that are ?100–150 K above their individual T{sub g}s. Four different solute probes providing a good spread of fluorescence lifetimes have been employed in steady state measurements, revealing strong excitation wavelength dependence of probe fluorescence emission peak frequencies. Extent of this dependence, which shows sensitivity to anion identity, has been found to increase with increase of amide chain-length and decrease of probe lifetime. Time-resolved measurements reveal strong fractional power dependence of average rates for solute solvation and rotation with fraction power being relatively smaller (stronger viscosity decoupling) for DEs containing longer amide and larger (weaker decoupling) for DEs containing perchlorate anion. Representative all-atom molecular dynamics simulations of (CH{sub 3}CONH{sub 2} + LiX) DEs at different temperatures reveal strongly stretched exponential relaxation of wavevector dependent acetamide self dynamic structure factor with time constants dependent both on ion identity and temperature, providing justification for explaining the fluorescence results in terms of temporal heterogeneity and amide clustering in these multi-component melts.

Guchhait, Biswajit; Das, Suman; Daschakraborty, Snehasis; Biswas, Ranjit, E-mail: ranjit@bose.res.in [Department of Chemical, Biological and Macromolecular Sciences, S. N. Bose National Centre for Basic Sciences, Block-JD, Sector-III, Salt Lake, Kolkata 700098 (India)] [Department of Chemical, Biological and Macromolecular Sciences, S. N. Bose National Centre for Basic Sciences, Block-JD, Sector-III, Salt Lake, Kolkata 700098 (India)

2014-03-14T23:59:59.000Z

203

Caenorhabditis elegans orthologs of the aryl hydrocarbon receptor and its heterodimerization partner the aryl hydrocarbon receptor nuclear translocator  

Science Journals Connector (OSTI)

...WI 53706 The aryl hydrocarbon receptor (AHR) is...The mammalian aryl hydrocarbon receptor (AHR) is...complex with the 90-kDa heat shock protein (HSP90) and...polycyclic aromatic hydrocarbons such as {beta...cigarette smoking and other combustion processes, initiate...

Jo Anne Powell-Coffman; Christopher A. Bradfield; William B. Wood

1998-01-01T23:59:59.000Z

204

Caenorhabditis elegans orthologs of the aryl hydrocarbon receptor and its heterodimerization partner the aryl hydrocarbon receptor nuclear translocator  

Science Journals Connector (OSTI)

...mammalian aryl hydrocarbon receptor...the 90-kDa heat shock protein (HSP90...polycyclic aromatic hydrocarbons such as {beta...smoking and other combustion processes...we searched data from the...Helminth HSP90 Heat-Shock Proteins...Molecular Sequence Data Protein Binding...Receptors, Aryl Hydrocarbon genetics metabolism...

Jo Anne Powell-Coffman; Christopher A. Bradfield; William B. Wood

1998-01-01T23:59:59.000Z

205

Composition of paraffinic and naphthenic hydrocarbons in petroleum asphalts  

SciTech Connect

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

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

1982-11-01T23:59:59.000Z

206

Ligand Lone-Pair Influence on Hydrocarbon C-H Activation: A Computational Perspective  

SciTech Connect

Mid to late transition metal complexes that break hydrocarbon C?H bonds by transferring the hydrogen to a heteroatom ligand while forming a metal?alkyl bond offer a promising strategy for C?H activation. Here we report a density functional (B3LYP, M06, and X3LYP) analysis of cis-(acac){sub 2}MX and TpM(L)X (M = Ir, Ru, Os, and Rh; acac = acetylacetonate, Tp = tris(pyrazolyl)borate; X = CH{sub 3}, OH, OMe, NH{sub 2}, and NMe{sub 2}) systems for methane C?H bond activation reaction kinetics and thermodynamics. We address the importance of whether a ligand lone pair provides an intrinsic kinetic advantage through possible electronic d{sub ?}?p{sub ?} repulsions for M?OR and M?NR{sub 2} systems versus M?CH{sub 3} systems. This involves understanding the energetic impact of the X ligand group on ligand loss, C?H bond coordination, and C?H bond cleavage steps as well as understanding how the nucleophilicity of the ligand X group, the electrophilicity of the transition metal center, and cis-ligand stabilization effect influence each of these steps. We also explore how spectator ligands and second- versus third-row transition metal centers impact the energetics of each of these C?H activation steps.

Ess, Daniel H; Gunnoe, T. Brent; Cundari, Thomas R; Goddard, William A; Periana, Roy A

2010-01-01T23:59:59.000Z

207

Benchmark Evaluation of Plutonium Nitrate Solution Arrays  

SciTech Connect

In October and November of 1981 thirteen approach-to-critical experiments were performed on a remote split table machine (RSTM) in the Critical Mass Laboratory of Pacific Northwest Laboratory (PNL) in Richland, Washington, using planar arrays of polyethylene bottles filled with plutonium (Pu) nitrate solution. Arrays of up to sixteen bottles were used to measure the critical number of bottles and critical array spacing with a tight fitting Plexiglas{reg_sign} reflector on all sides of the arrays except the top. Some experiments used Plexiglas shells fitted around each bottles to determine the effect of moderation on criticality. Each bottle contained approximately 2.4 L of Pu(NO3)4 solution with a Pu content of 105 g Pu/L and a free acid molarity H+ of 5.1. The plutonium was of low 240Pu (2.9 wt.%) content. These experiments were performed to fill a gap in experimental data regarding criticality limits for storing and handling arrays of Pu solution in reprocessing facilities. Of the thirteen approach-to-critical experiments eleven resulted in extrapolations to critical configurations. Four of the approaches were extrapolated to the critical number of bottles; these were not evaluated further due to the large uncertainty associated with the modeling of a fraction of a bottle. The remaining seven approaches were extrapolated to critical array spacing of 3-4 and 4-4 arrays; these seven critical configurations were evaluation for inclusion as acceptable benchmark experiments in the International Criticality Safety Benchmark Evaluation Project (ICSBEP) Handbook. Detailed and simple models of these configurations were created and the associated bias of these simplifications was determined to range from 0.00116 and 0.00162 {+-} 0.00006 ?keff. Monte Carlo analysis of all models was completed using MCNP5 with ENDF/BVII.0 neutron cross section libraries. A thorough uncertainty analysis of all critical, geometric, and material parameters was performed using parameter perturbation methods. It was found that uncertainty in the impurities in the polyethylene bottles, reflector position, bottle outer diameter, and critical array spacing had the largest effect. The total uncertainty ranged from 0.00651 to 0.00920 ?keff. Evaluation methods and results will be presented and discussed in greater detail in the full paper.

M. A. Marshall; J. D. Bess

2011-09-01T23:59:59.000Z

208

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

209

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

210

LUMINESCENCE SPECTRA OF THE URANYL ION IN TWO GEOMETRICALLY SIMILAR COORDINATION ENVIRONMENTS: URANYL NITRATE HEXAHYDRATE AND DI-u-AQUO-BIS (DIOXODINITRA-TOURANIUM(VI) DI-IMIDAZOLE  

E-Print Network (OSTI)

coordination sphere of uranyl nitrate hexahydrate (UNH). U-Coordination Environments: Uranyl Nitrate Hexahydrate andin the crystal hosts of uranyl nitrate hexahydrate (UNH) and

Brittain, Harry G.

2013-01-01T23:59:59.000Z

211

Spin Crossover in a Series of Iron(II) Complexes of 2-(2-Alkyl-2H-tetrazol-5-yl)-1,10-phenanthroline: Effects of Alkyl Side  

E-Print Network (OSTI)

Spin Crossover in a Series of Iron(II) Complexes of 2-(2-Alkyl-2H-tetrazol-5-yl)-1Versity, Beijing 100871, China Received October 27, 2006 2-(2H-Tetrazol-5-yl)-1,10-phenanthroline (HL0 ), its alkyl) at the 2H position of the tetrazole ring, and their iron(II) complexes (a for [Fe(L0 )2], na for [Fe(Ln)2

Gao, Song

212

Thermophysical Properties of Sodium Nitrate and Sodium Chloride  

Office of Scientific and Technical Information (OSTI)

Thermophysical Properties of Sodium Nitrate and Sodium Chloride Thermophysical Properties of Sodium Nitrate and Sodium Chloride Solutions and Their Effects on Fluid Flow in Unsaturated Media Tianfu Xu and Karsten Pruess Earth Sciences Division, Lawrence Berkeley National Laboratory, University of California, Berkeley, CA 94720 ABSTRACT. Understanding movement of saline sodium nitrate (NaNO 3 ) waste solutions is important for assessing the contaminant migration near leaking waste storage tanks in the unsaturated zone at the Hanford site (Washington, USA). The purpose of this study is to contribute a basic understanding of effects of the thermophysical behavior of NaNO 3 solutions on fluid flow in unsaturated media. We first present mathematical expressions for the dependence of density, viscosity, solubility and vapor pressure of

213

Thorium Nitrate Stockpile--From Here to Eternity  

SciTech Connect

The Defense National Stockpile Center (DNSC), a field level activity of the Defense Logistics Agency (DLA) has stewardship of a stockpile of thorium nitrate that has been in storage for decades. The stockpile is made up of approximately 3.2 million kg (7 million lb) of thorium nitrate crystals (hydrate form) stored at two depot locations in the United States. DNSC sought technical assistance from Oak Ridge National Laboratory (ORNL) to define and quantify the management options for the thorium nitrate stockpile. This paper describes methodologies and results comprising the work in Phase 1 and Phase 2. The results allow the DNSC to structure and schedule needed tasks to ensure continued safe long-term storage and/or phased disposal of the stockpile.

Hermes, W. H.; Hylton, T. D.; Mattus, C.H.; Storch, S. N.; Singley, P.S.; Terry. J. W.; Pecullan, M.; Reilly, F. K.

2003-02-26T23:59:59.000Z

214

HYDROCARBONS FROM PLANTS: ANALYTICAL METHODS AND OBSERVATIONS  

SciTech Connect

We have suggested that certain plants rich in hydrocarbon-like materials might be cultivated for renewable photosynthetic products. Two species were selected for experimental plantations: Euphorbia lathyris, an annual from seed and Euphorbia tirucalli, a perennial from cuttings, The yield from each species is over 10 barrels of oil/acre/year without genetic or agronomic improvement. In addition to plants, there are trees, such as species of Copaifera in Brazil and other tropical areas, which produce a diesel-like oil upon tapping. Each tree produces approximately 40 liters of hydrocarbon per year, and this material can be used directly by a diesel-powered car. Further efforts to develop plants as alternate energy sources are underway, as well as a continuing search for additional plant species throughout the world which have a similar capability.

Calvin, Melvin

1980-05-01T23:59:59.000Z

215

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

216

Getter pump for hydrogen and hydrocarbon gases  

DOE Patents (OSTI)

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

Hsu, Wen Ling

1987-10-14T23:59:59.000Z

217

Field Validation of Polyethylene Passive Air Samplers for Parent and Alkylated PAHs in Alexandria, Egypt  

Science Journals Connector (OSTI)

Field Validation of Polyethylene Passive Air Samplers for Parent and Alkylated PAHs in Alexandria, Egypt ... In Alexandria for example, eight monitoring stations were established for monitoring the atmospheric quality since the establishment of the Egyptian environmental Law (Law No. 4, 1994). ... Environmental Characterization of Alexandria, Egypt; Egyptian Environmental Affairs Agency: Cairo, 2007; www.eeaa.gov.eg/English/reports/GovProfiles/final/Alex%20Des.pdf. ...

Mohammed A. Khairy; Rainer Lohmann

2012-03-07T23:59:59.000Z

218

Summary of Substitution and Elimination Reactions of Alkyl Halides Polar protic solvent  

E-Print Network (OSTI)

will come from E2 and/or SN2, or there will be no reaction, depending upon the structure of the alkyl halide­X E2, SN2, E1/SN1 First, you need to know which products to expect from each mechanism. Second, you: 1) 1° halides will give SN2 unless the halide is hindered on the backside by branching

Walba, David

219

STRUCTURE OF PENTAKIS (UREA) DIOXOURANIUM(VI)NITRATE LUO2 (OC (NH2)2)5 (NO3) 2  

E-Print Network (OSTI)

an aqueous solution of uranyl nitrate and urea which wasALL f(O,O.t» URANYL UREA NITRATE FOB AND FCA ARE THEFACTORS CO~TINUE& FOf URANYL UREA NITRATE l F[) B PAGE . ,

Zalkin, Allan

2011-01-01T23:59:59.000Z

220

E-Print Network 3.0 - aluminium nitrates Sample Search Results  

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

common co.contaminant with uranium. Nitrate inhib- ited U... Mexico. Once nitrate was depleted, both U(VI) and Fe(lIl) were Ireduced concurrently. When ... Source: Lovley, Derek -...

Note: This page contains sample records for the topic "hydrocarbons alkyl nitrates" 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

THE SYSTEM THORIUM NITRATE-WATER-NITRIC ACID AT 25 AND THE HYDRATES...  

Office of Scientific and Technical Information (OSTI)

SYSTEM THORIUM NITRATE-WATER-NITRIC ACID AT 25 AND THE HYDRATES OF THORIUM NITRATE Re-direct Destination: Temp Data Fields Ferraro, J.R.; Katzin, L.I. Temp Data Storage 3: Argonne...

222

Extraction of U(VI) with N,N?-dimethyl-N,N?-dioctylmalonamide from nitrate media  

Science Journals Connector (OSTI)

The extraction of uranyl nitrate with the novel extractant N,N?-dimethyl-N,N?-dioctylmalonamide (DMDOMA) from aqueous sodium nitrate (and nitric acid) was investigated. The extraction mechanism was established an...

Yu Cui; Yufen Hu; Yanju Zhang; Shaohong Yin…

2010-03-01T23:59:59.000Z

223

Nitrate occurrence and attenuation in the major aquifers of England and Wales  

Science Journals Connector (OSTI)

...Examination of the delta15N composition of infiltrating nitrate relative...L., Zech, W., The composition of dissolved organic matter...Migration and attenuation of agrochemical pollutants: insights from...The nitrogen isotope composition of groundwater nitrates from...

M.O. Rivett; J.W.N. Smith; S.R. Buss; P. Morgan

224

E-Print Network 3.0 - ammonium nitrate-fuel oil Sample Search...  

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

nitrate-fuel oil Search Powered by Explorit Topic List Advanced Search Sample search results for: ammonium nitrate-fuel oil Page: << < 1 2 3 4 5 > >> 1 ORNL 2010-G01068jcn UT-B ID...

225

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

226

Waste Isolation Pilot Plant Nitrate Salt Bearing Waste Container  

E-Print Network (OSTI)

HEPA filtration. On April 11, 2014, in anticipation of investigation of the source of a radiological on the possibility that a container of inadequately remediated nitrate salt bearing waste had caused the release and is the most Page 1 of 17 #12;likely source of the release. Further investigation is underway to determine

Napp, Nils

227

Catalytic Upgrading of Sugars to Hydrocarbons Technology Pathway  

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

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

228

Biological Conversion of Sugars to Hydrocarbons Technology Pathway...  

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

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

229

CSIA of Petroleum Hydrocarbons: Forensic Fingerprinting and Oil Spill Characterisation.  

E-Print Network (OSTI)

??This thesis has identified a suite of hydrocarbon diagnostic indices to be applied in the forensic fingerprinting of diesel oil characterisation and source identification using… (more)

Muhammad, Syahidah Akmal binti

2012-01-01T23:59:59.000Z

230

The mobility of petroleum hydrocarbons in Athabasca oil sands tailings.  

E-Print Network (OSTI)

??Several oil sands tailings from Suncor Energy Inc. were analysed with respect to the mobility and solubility of the petroleum hydrocarbon (PHC) contaminants. At sites… (more)

Brickner, Heather

2014-01-01T23:59:59.000Z

231

Process for making unsaturated hydrocarbons using microchannel process technology  

DOE Patents (OSTI)

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

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

2011-04-12T23:59:59.000Z

232

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

233

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

234

Selective aerobic oxidation of hydrocarbons over supported gold catalysts.  

E-Print Network (OSTI)

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

Hereijgers, B.P.C.

2011-01-01T23:59:59.000Z

235

Catalytic Upgrading of Sugars to Hydrocarbons Technology Pathway...  

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

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

236

Mechanisms of Hydrocarbon Poisoning of A Urea SCR Catalyst  

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

Understanding what reactions and which catalytic functions are affected by hydrocarbons can lead to improved tolerances for selective catalytic reduction performance

237

Electrical dispersion of water drops suspended in hydrocarbons  

Science Journals Connector (OSTI)

The effects of alternating (50 Hz) and direct current fields on drops of distilled water in a nonpolar hydrocarbon medium were examined.

G. M. Panchenkov; V. V. Papko; V. Ya. Baranov

1968-10-01T23:59:59.000Z

238

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

239

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

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

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

240

Nitrate Enhanced Microbial Cr(VI) Reduction-Final Report  

SciTech Connect

A major challenge for the bioremediation of radionuclides (i.e., uranium, technetium) and metals (i.e., Cr(VI), Hg) is the co-occurrence of nitrate as it can inhibit metal transformation. Denitrification (nitrate reduction to dinitrogen gas) is considered the most important ecological process. For many metal and metalloid reducing bacteria, however, ammonia is the end product through respiratory nitrate reduction (RNRA). The focus of this work was to determine how RNRA impacts Cr(VI) transformation. The goal was to elucidate the specific mechanism(s) that limits Cr(VI) reduction in the presence of nitrate and to use this information to develop strategies that enhance Cr(VI) reduction (and thus detoxification). Our central hypothesis is that nitrate impacts the biotransformation of metals and metalloids in three ways 1) as a competitive alternative electron acceptor (inhibiting transformation), 2) as a co-metabolite (i.e., concomitant reduction, stimulating transformation), and 3) as an inducer of specific proteins and pathways involved in oxidation/reduction reactions (stimulating transformation). We have identified three model organisms, Geobacter metallireducens (mechanism 1), Sulfurospirillum barnesii, (mechasism 2), and Desulfovibrio desulfuricans (mechanisms 3). Our specific aims were to 1) investigate the role of Cr(VI) concentration on the kinetics of both growth and reduction of nitrate, nitrite, and Cr(VI) in these three organisms; 2) develop a profile of bacterial enzymes involved in nitrate transformation (e.g., oxidoreductases) using a proteomic approach; 3) investigate the function of periplasmic nitrite reductase (Nrf) as a chromate reductase; and 4) develop a strategy to maximize microbial chromium reduction in the presence of nitrate. We found that growth on nitrate by G. metallireducens was inhibited by Cr(VI). Over 240 proteins were identified by LC/MS-MS. Redox active proteins, outer membrane heavy metal efflux proteins, and chemotaxis sensory proteins (Gmet_2478 and Gmet_1641) were up-regulated with exposure to Cr(VI). A nine-heme cytochrome C was purified that could reduce nitrite and could be oxidized by Cr(VI). For D. desulfuricans, we found that confirmed that Cr(VI) induced a prolonged lag period when Cr(VI) was reduced. Over three hundred proteins were unequivocally identified by LC/MS-MS and a significant number of down-regulated proteins for which the levels were changed >2 fold compared to control. Sulfite reductase levels were similar, however, nitrate and nitrite reductase were down-regulated. The supernatant of spent cultures was found to contain a filterable, heat stable compound that rapidly reduced Cr(VI). In addition, desulfoviridin was purified from nitrate grown cells and shown to have nitrite reductase activity that was inhibited by Cr(VI). For S. barnesii, periplasmic nitrate reductase (Nap), nitrite reductase (Nrf), and the metalloid reductase (Rar) were purified and characterized. The supernatant of spent cultures was also found to contain a filterable, heat stable compound that rapidly reduced Cr(VI) but that Rar also reduced Cr(VI). Our results from specific aims 1 through 3 indicate that for G. metallireducens, Cr(VI) inhibits nitrate respiration as it oxidizes cytochromes involved in nitrate respiration. Iron reduction is apparently not affected and the inhibitory affects of Cr(VI) may be attenuated by the addition of sufficient Fe(III) to generate Fe(II) that abiotically reduces the chromium. For S. barnesii, although the enzyme assays indicate that the components of the respiratory pathway for nitrate (e.g. Nap and Nrf) are inhibited by chromate, the organism has a mechanism to prevent this from actually occurring. Our current hypothesis is that the non-specific metalloid reductase (Rar) is providing resistance by reducing the Cr(VI). The strategy here would be to enhance its growth and metabolism in the natural setting. Lactate is a suitable electron donor for S. barnesii but other donors are possible. Although the version of the Phylochip used for monitoring the microb

John F. Stolz

2011-06-15T23:59:59.000Z

Note: This page contains sample records for the topic "hydrocarbons alkyl nitrates" 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

Optimizing hydrocarbon recoveries in nitrogen rejection units  

SciTech Connect

In order to address conceptual questions such as process selection and natural gas liquids plant integration, an understanding of the effects of several additional factors on nitrogen rejection unit design is important. These factors, which may influence optimum hydrocarbon recovery, installed compression, etc., include current and forecast values for natural gas and utilities, project life, plant size, feed gas composition and product specifications, feed pressure, and process variations. Prices, project life, and plant size are analyzed in detail and presented in terms of methane recoveries as a function of nitrogen content in the feed for both double and single column processes. Trends are qualitatively discussed for the remaining factors. 13 references.

Chesney, J.D.; Davis, R.A.; Hilton, M.F.; Vines, H.L.

1983-01-01T23:59:59.000Z

242

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

243

Mutagenicity of Soot and Associated Polycyclic Aromatic Hydrocarbons to Salmonella typhimurium  

Science Journals Connector (OSTI)

...polycyclic aromatic hydrocarbons were quantitatively...polycyclic aromatic hydrocarbon constituent in a kerosene...polycyclic aromatic hydrocarbon fraction in terms of...formed by the incomplete combustion of organic material...and sediments (1), heat and power generation...

Debra A. Kaden; Ronald A. Hites; and William G. Thilly

1979-10-01T23:59:59.000Z

244

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

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

various hydrocarbons on monolithic hydrocarbon adsorber Dae Jung Kim,a Ji Man Kim,a Jae Eui Yie... and conversion of various hydrocarbons on ... Source: Kim, Ji Man - Department...

245

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

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

various hydrocarbons on monolithic hydrocarbon adsorber Dae Jung Kim,a Ji Man Kim,a Jae Eui Yie... and conversion of various hydrocarbons on ... Source: Kim, Ji Man - Department...

246

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

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

various hydrocarbons on monolithic hydrocarbon adsorber Dae Jung Kim,a Ji Man Kim,a Jae Eui Yie... and conversion of various hydrocarbons on ... Source: Kim, Ji Man - Department...

247

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

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

various hydrocarbons on monolithic hydrocarbon adsorber Dae Jung Kim,a Ji Man Kim,a Jae Eui Yie... and conversion of various hydrocarbons on monolithic ... Source: Kim, Ji Man -...

248

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

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

various hydrocarbons on monolithic hydrocarbon adsorber Dae Jung Kim,a Ji Man Kim,a Jae Eui Yie... and conversion of various hydrocarbons on monolithic ... Source: Kim, Ji Man -...

249

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

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

various hydrocarbons on monolithic hydrocarbon adsorber Dae Jung Kim,a Ji Man Kim,a Jae Eui Yie... and conversion of various hydrocarbons on monolithic ... Source: Kim, Ji Man -...

250

The Fate of Fossil Fuel Hydrocarbons in Marine Animals [and Discussion  

Science Journals Connector (OSTI)

...research-article The Fate of Fossil Fuel Hydrocarbons in Marine Animals [and Discussion...mammals. The fate of fossil fuel hydrocarbons in marine animals. | Journal Article...Carcinogens 0 Epoxy Compounds 0 Fuel Oils 0 Hydrocarbons 0 Naphthalenes...

1975-01-01T23:59:59.000Z

251

Ozonation of Mutagenic and Carcinogenic Polyaromatic Amines and Polyaromatic Hydrocarbons in Water  

Science Journals Connector (OSTI)

...Amines and Polyaromatic Hydrocarbons in Water 1 1 Supported by a grant...amines and polyaromatic hydrocarbons in water. | The Salmonella-microsome...g., 13 halogenated hydrocarbons were identified in the drinking water of New Orleans (13...

Gary R. Burleson; Michael J. Caulfield; and Morris Pollard

1979-06-01T23:59:59.000Z

252

Determination of hydrocarbons in water – interlaboratory method validation before routine monitoring  

Science Journals Connector (OSTI)

The clarification of hydrocarbon input into the Baltic sea via rivers ... of a new method for the determination of hydrocarbons by solvent extraction and gas chromatography. Surrogate oil solutions with known hydrocarbon

P. Woitke; Reinhard Kreßner; Peter Lepom

2001-04-01T23:59:59.000Z

253

Process for using preferential physical solvents for selective processing of hydrocarbon gas streams  

SciTech Connect

This patent describes a process for the removal of hydrocarbon gas liquids, comprising hydrocarbons heavier than methane, from a hydrocarbon gas stream, wherein a need exists for recovering to any selected degree and at extremely high recoveries a selected hydrocarbon component and heavier hydrocarbons. The hydrocarbons are within the group consisting of ethane, propane, butane, and pentane without the need simultaneously to recover hydrocarbons lighter than the selected hydrocarbon component from the hydrocarbon gas stream, The improvement of selectively extracting the hydrocarbon gas liquids from the hydrocarbon gas stream with a preferential physical solvent is described here. The method provides selective capability for recovery according to the selected degree of (a) ethane in amounts ranging from 2-98%, (b) propane in amounts ranging from 2-99%, (c) butane in amounts ranging from 2-100%, or (d) pentanes and higher molecular weight hydrocarbons in amounts ranging up to 100%.

Mehra, Y.R.

1986-10-14T23:59:59.000Z

254

Hydrocarbon steam reforming using series steam superheaters  

SciTech Connect

In a process for steam reforming of a hydrocarbon gas feedstream wherein: the hydrocarbon gas feedstream is partially reformed at elevated temperatures in indirect heat exchange with hot combustion gases in a direct fired primary reforming furnace provided with a convection section for recovery of excess heat from said combustion gases; and the partially reformed feedstream is then further reformed in the presence of an oxygen-containing gas and steam in a secondary reformer to form a secondary reformer gaseous effluent; the improvement which comprises recovering waste heat from said secondary reformer effluent gas and from said primary reforming combustion products by heating a high pressure saturated steam in a first steam superheating zone by indirect heat exchange with at least a portion of said secondary reformer effluent gas to form a first superheated steam stream; and further heating said first superheated steam in a second steam superheating zone by indirect heat exchange with at least a portion of said primary reformer hot combustion gases for form a second superheated steam stream.

Osman, R. M.

1985-10-08T23:59:59.000Z

255

Algal Lipid Extraction and Upgrading to Hydrocarbons Technology Pathway  

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

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.

256

Scroll compressor modelling for heat pumps using hydrocarbons as refrigerants  

E-Print Network (OSTI)

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

Paris-Sud XI, Université de

257

Contemplation on the heats of combustion of isomeric hydrocarbons  

Science Journals Connector (OSTI)

Within the Hückel molecular orbital theory, the heats of combustion of isomeric hydrocarbons are related to some topological factors. The standard heats of combustion values of alternant hydrocarbons, expressed as kcal/g, seem to be related to a4 coefficient of their secular polynomials.

Lemi Türker

2004-01-01T23:59:59.000Z

258

Formation mechanism for polycyclic aromatic hydrocarbons in methane flames  

E-Print Network (OSTI)

aromatic hydrocarbons PAHs up to 788 amu (C64H20) were detected in the combustion gases. Only the most applications including heating systems and gas turbines for electric power generation.62­64 The combustionFormation mechanism for polycyclic aromatic hydrocarbons in methane flames K. Siegmanna) Swiss

Sattler, Klaus

259

Biological Conversion of Sugars to Hydrocarbons Technology Pathway  

SciTech Connect

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

260

Biological Conversion of Sugars to Hydrocarbons Technology Pathway  

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

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.

Note: This page contains sample records for the topic "hydrocarbons alkyl nitrates" 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

High levels of carcinogenic polycyclic aromatic hydrocarbons in mate drinks  

Science Journals Connector (OSTI)

...carcinogenic polycyclic aromatic hydrocarbons in mate drinks Farin Kamangar...exposure to polycyclic aromatic hydrocarbons (PAHs), including known...80 oC) or cold (4 oC) water and two commonly used brands...Infusions were made by adding water to the leaves, steeping for...

Farin Kamangar; Michele Schantz; Christian Abnet; Renato Fagundes; and Sanford Dawsey

2008-05-01T23:59:59.000Z

262

Total Synthesis of Convex Polyhedral Hydrocarbons The Platonic Solids  

E-Print Network (OSTI)

O H H Total Synthesis of Convex Polyhedral Hydrocarbons The Platonic Solids O O t-BuO3C Br O O Br Br Ph PhPh Ph PhPh Ph Ph COOH HOOC Total Synthesis of Convex Polyhedral Hydrocarbons The Five Matter Icosahedron Water · Polyhedron: a closed surface made up of polygonal regions. · Regular

Stoltz, Brian M.

263

Natural attenuation of fuel hydrocarbon contaminants: Hydraulic conductivity dependency of biodegradation rates in a field case study  

SciTech Connect

Two biodegradation models are developed to represent natural attenuation of fuel-hydrocarbon contaminants as observed in a comprehensive natural-gradient tracer test in a heterogeneous aquifer on the Columbus Air Force Base in Mississippi. The first, a first-order mass loss model, describes the irreversible losses of BTEX and its individual components, i.e., benzene (B), toluene (T), ethyl benzene (E), and xylene (X). The second, a reactive pathway model, describes sequential degradation pathways for BTEX utilizing multiple electron acceptors, including oxygen, nitrate, iron and sulfate, and via methanogenesis. The heterogeneous aquifer is represented by multiple hydraulic conductivity (K) zones delineated on the basis of numerous flowmeter K measurements. A direct propagation artificial neural network (DPN) is used as an inverse modeling tool to estimate the biodegradation rate constants associated with each of the K zones. In both the mass loss model and the reactive pathway model, the biodegradation rate constants show an increasing trend with the hydraulic conductivity. The finding of correlation between biodegradation kinetics and hydraulic conductivity distributions is of general interest and relevance to characterization and modeling of natural attenuation of hydrocarbons in other petroleum-product contaminated sites.

Lu, Guoping; Zheng, Chunmiao

2003-07-15T23:59:59.000Z

264

Natural Attenuation of Fuel Hydrocarbon Contaminants: Correlation of Biodegradation with Hydraulic Conductivity in a Field Case Study  

SciTech Connect

Two biodegradation models are developed to represent natural attenuation of fuel-hydrocarbon contaminants as observed in a comprehensive natural-gradient tracer test in a heterogeneous aquifer on the Columbus Air Force Base in Mississippi, USA. The first, a first-order mass loss model, describes the irreversible losses of BTEX and its individual components, i.e., benzene (B), toluene (T), ethyl benzene (E), and xylene (X). The second, a reactive pathway model, describes sequential degradation pathways for BTEX utilizing multiple electron acceptors, including oxygen, nitrate, iron and sulfate, and via methanogenesis. The heterogeneous aquifer is represented by multiple hydraulic conductivity (K) zones delineated on the basis of numerous flowmeter K measurements. A direct propagation artificial neural network (DPN) is used as an inverse modeling tool to estimate the biodegradation rate constants associated with each of the K zones. In both the mass loss model and the reactive pathway model, the biodegradation rate constants show an increasing trend with the hydraulic conductivity. The finding of correlation between biodegradation kinetics and hydraulic conductivity distributions is of general interest and relevance to characterization and modeling of natural attenuation of hydrocarbons in other petroleum-product contaminated sites.

Lu, Guoping; Zheng, Chunmiao

2003-10-15T23:59:59.000Z

265

Role of alkyl alcohol on viscosity of silica-based chemical gels for decontamination of highly radioactive nuclear facilities  

SciTech Connect

Silica-based chemical gel for the decontamination of nuclear facilities was prepared by using fumed silica as a viscosifier, a 0.5 M Ce (IV) solution dissolved in concentrated nitric acid as a chemical decontamination agent, and tripropylene glycol butyl ether (TPGBE) as a co-viscosifier. A new effective strategy for the preparation of the chemical gel was investigated by introducing the alkyl alcohols as organic solvents to effectively dissolve the co-viscosifier. The mixture solution of the co-viscosifier and alkyl alcohols was more effective in the control of viscosity than that of the co-viscosifier only in gel. Here, the alkyl alcohols played a key role as an effective dissolution solvent for the co-viscosifier in the preparation of the chemical gel, resulting in a reducing of the amount of the co-viscosifier and gel time compared with that of the chemical gel prepared without the alkyl alcohols. It was considered that the alkyl alcohols contributed to the effective dissolution of the co-viscosifier as well as the homogeneous mixing in the formation of the gel, while the co-viscosifier in an aqueous media of the chemical decontamination agent solution showed a lower solubility. The decontamination efficiency of the chemical gels prepared in this work using a multi-channel analyzer (MCA) showed a high decontamination efficiency of over ca. 94% and ca. 92% for Co-60 and Cs-137 contaminated on surface of the stainless steel 304, respectively. (authors)

Choi, B. S.; Yoon, S. B.; Jung, C. H.; Lee, K. W.; Moon, J. K. [Div. of Decontamination and Decommissioning Technology Development, Korea Atomic Energy Research Inst., Daedeok-daero 989-111, Yuseong-gu, Daejeon, 305-353 (Korea, Republic of)

2012-07-01T23:59:59.000Z

266

Microbial Degradation in Soil Microcosms of Fuel Oil Hydrocarbons from Drilling Cuttings  

Science Journals Connector (OSTI)

Microbial Degradation in Soil Microcosms of Fuel Oil Hydrocarbons from Drilling Cuttings ... Relation between Bioavailability and Fuel Oil Hydrocarbon Composition in Contaminated Soils ...

Claude-Henri. ChaIneau; Jean-Louis. Morel; Jean. Oudot

1995-06-01T23:59:59.000Z

267

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

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

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

268

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

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

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

269

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

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

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

270

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

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

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

271

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

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

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

272

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

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

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

273

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

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

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

274

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

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

275

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

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

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

276

Chlorinated C$_{1}$ and C$_{2}$ Hydrocarbons in the Marine Environment [and Discussion  

Science Journals Connector (OSTI)

...the marine environment. | Journal Article | 0 Hydrocarbons, Chlorinated | Air Pollution analysis Animals Fresh Water Great Britain Hydrocarbons, Chlorinated analysis metabolism Seawater Water Pollution, Chemical analysis The Royal Society...

1975-01-01T23:59:59.000Z

277

A generalized viscosity equation for pure heavy hydrocarbons  

SciTech Connect

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

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

1991-02-01T23:59:59.000Z

278

Bioremediation of soil contaminated with hydrocarbons and heavy metals  

SciTech Connect

This investigation showed that a soil contaminated with petroleum hydrocarbons and heavy metals had sufficient indigenous microbial activity for hydrocarbon biodegradation under nonlimiting conditions. Nutrient supplementation with nitrogen and phosphate, together with aeration, seemed to be the most important factors for enhancing biodegradation. Hydrocarbon biodegradation occurred to a much greater extent under aerobic than under anaerobic conditions. Biodegradation did, however, induce low pH conditions and thus caused high heavy-metal concentrations in the leachate. Anaerobic conditions inhibited hydrocarbon biodegradation with no subsequent drop in pH and low heavy-metal concentrations in the leachate. Thus, anaerobic conditions were shown to facilitate less metal mobility than low pH conditions. Air sparging did not cause a significant increase in biodegradation. Adsorption of heavy-fraction hydrocarbons (> C{sub 20}) to microorganisms and colloidal material in the leachate was suspected of facilitating mobility of these fractions and thus their subsequent detection in the leachate.

Plessis, C.A. du; Phaal, C.B.; Senior, E. [Univ. of Natal, Scottsville (South Africa)

1995-12-31T23:59:59.000Z

279

Cogeneration systems and processes for treating hydrocarbon containing formations  

DOE Patents (OSTI)

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

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

2009-12-29T23:59:59.000Z

280

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

Note: This page contains sample records for the topic "hydrocarbons alkyl nitrates" 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

Total Carbon Dioxide, Hydrographic, and Nitrate Measurements in the  

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

Total Carbon Dioxide, Hydrographic, and Nitrate Measurements in the Southwest Pacific during Austral Autumn, 1990: Results from NOAA/PMEL CGC-90 Cruise. Total Carbon Dioxide, Hydrographic, and Nitrate Measurements in the Southwest Pacific during Austral Autumn, 1990: Results from NOAA/PMEL CGC-90 Cruise. NDP-052 (1995) data Download the Data and ASCII Documentation files of NDP-052 PDF Download a PDF of NDP-052 image Contributed by Marilyn F. Lamb and Richard A. Feely Pacific Marine Environmental Laboratory Seattle, Washington and Lloyd Moore and Donald K. Atwood Atlantic Oceanographic and Meteorological Laboratory Miami, Florida Prepared by Alexander Kozyr* Carbon Dioxide Information Analysis Center Oak Ridge National Laboratory Oak Ridge, Tennessee, U.S.A. *Energy, Environment, and Resources Center The University of Tennessee Knoxville, Tennessee Environmental Sciences Division Publication No. 4420 Date Published: September 1995

282

Infrared absorption coefficients of gaseous chlorine nitrate at 296 K  

SciTech Connect

Chlorine nitrate (ClONO{sub 2}) is a temporary reservoir species which couples the ClO{sub x} and NO{sub x} catalytic cycles responsible for ozone depletion in the stratosphere. The identification and quantitative estimation of ClONO{sub 2} in the stratosphere has been achieved using its characteristic absorptions around 1,292 cm{sup {minus}1}. Peak and integrated absorption coefficients of the {nu}{sub 1}, {nu}{sub 2}, {nu}{sub 3} and {nu}{sub 4} fundamental bands of chlorine nitrate were measured at resolutions of 0.13 cm{sup {minus}1} for both pure and pressure-broadened samples at 296 K. The results are compared to previous literature data.

Tuazon, E.C. (Univ. of California, Riverside (USA)); Wallington, T.J. (Ford Motor Co., Dearborn, MI (USA))

1989-04-01T23:59:59.000Z

283

ADSORPTION/DESORPTION STUDIES ON SOLID ACID ALKYLATION CATALYSTS USING A TAPERED ELEMENT OSCILLATING MICROBALANCE (TEOM)  

E-Print Network (OSTI)

for the first time the adsorption/desorption characteristics of alkylation reactants and products on these zeolites and some mesoporous materials. Equilibrium adsorption isotherms were obtained on these catalysts using n-butane, isobutane, and propane....2.1. Zeolites 72 4.2.2. Mesoporous Materials 78 4.2.3. Chemicals 79 vi 4.3. Equilibrium Adsorption Isotherms of n-Butane, Isobutane, and Propane on b- zeolite and USY-zeolite 79 4.4. Equilibrium Adsorption Isotherms of CO2 on b-zeolite and USY-zeolite 89 4...

Gong, Kening

2008-10-23T23:59:59.000Z

284

for the alkylation reaction. We (23) and others (24) observed similar carbon isotope effects in  

E-Print Network (OSTI)

no wasteful by-products other than water. Whereas chlorinated solvents such as CH2Cl2 and C6H5Cl generally give the best results, nonchlorinated solvents such as toluene and tetrahydrofuran can be used in most- generation "green" catalytic processes. References and Notes 1. G. A. Olah, A. Molnár, Hydrocarbon Chemistry

Jacob, Daniel J.

285

Process for steam reforming of hydrocarbons  

SciTech Connect

A process is provided for the steam reforming of normally liquid hydrocarbons to produce carbon monoxide and hydrogen, which does not promote the deposition of carbonacious materials upon catalytic surfaces. The catalyst consists of nickel promoted with the oxides of iron and manganese within a specific manganese to iron ratio, said metal and metal oxides being supported upon a refractory support. The support is preferably aluminum oxide in its alpha phase having a surface area of more than 0.5 m2/gm but no more than 10 m2/gm. The metallic constituents are impregnated onto said refractory low surface area support as salts and are calcined at sufficiently high temperature to convert the salts to the oxide but at a sufficiently low temperature that they do not chemically react with the support.

Broughton, D.R.; Russ, K.J.

1980-11-11T23:59:59.000Z

286

Method and apparatus for detecting halogenated hydrocarbons  

DOE Patents (OSTI)

A halogenated hydrocarbon (HHC) detector is formed from a silent discharge (also called a dielectric barrier discharge) plasma generator. A silent discharge plasma device receives a gas sample that may contain one or more HHCs and produces free radicals and excited electrons for oxidizing the HHCs in the gas sample to produce water, carbon dioxide, and an acid including halogens in the HHCs. A detector is used to sensitively detect the presence of the acid. A conductivity cell detector combines the oxidation products with a solvent where dissociation of the acid increases the conductivity of the solvent. The conductivity cell output signal is then functionally related to the presence of HHCs in the gas sample. Other detectors include electrochemical cells, infrared spectrometers, and negative ion mobility spectrometers.

Monagle, Matthew (Los Alamos, NM); Coogan, John J. (Los Alamos, NM)

1997-01-01T23:59:59.000Z

287

Experimental Investigations of an IC Engine Operating with Alkyl Esters of Jatropha, Karanja and Castor Seed Oil  

Science Journals Connector (OSTI)

Abstract Diesel engines are efficient systems popularly used to meet electricity and other power requirements for agriculture, industry, transportation and decentralized power generation. Vegetable oils can be successfully used in Compression Ignition (CI) engine either through engine modifications or fuel modifications, later being more feasible option. Fuel modification options include blending of vegetable oils with mineral diesel, transesterification, cracking/pyrolysis, micro-emulsion, and hydrogenation to reduce polymerization and viscosity, transesterification of vegetable oil with a short chain alcohol i.e. methanol or ethanol being most popular. Several non-edible plant oils have been found to be promising crude oils for the production of biodiesel. Methanol is most commonly used in commercial production of biodiesel. Fatty acid alkyl esters (FAAE) produced from higher alcohols is of interest as they may have different fuel properties in comparison to methyl or ethyl esters. In the present investigations, preparation of methanol, ethanol, propanol and butanol were used for formation of alkyl esters of Jatropha, Karanja and Castor. The composition of Jatropha, Karanja and Castor oil were analysed and alcoholysis process for preparing alkyl esters of Jatropha, Karanja and Castor oil with various alcohols was optimised. Alkyl ester-diesel blends were used to test the diesel engine at different load conditions and extensive performance and emissions studies were conducted in single cylinder direct injection compression ignition engines. It is concluded that lower blends of ethyl, propyl and butyl esters of Jatropha and Karanja feedstock have physico-chemical properties similar to methyl esters. However, deviation from the properties became larger for higher blending ratio. Therefore, in order to get engine performance in close range of diesel, the optimum blending ratio of higher alkyl esters need to be even less than methyl esters. Lower blends of higher alkyl esters are expected to give engine characteristics in close proximity to diesel overcoming the limitations of bio-diesel, while retaining the advantages.

Sanjay Bajpai; Lalit Mohan Das

2014-01-01T23:59:59.000Z

288

Synthesis and chemistry of cationic d sup 0 metal alkyl complexes  

SciTech Connect

The objective of this project is to develop new types of electrophilic metal alkyl complexes for catalytic C-H activation and olefin polymerization chemistry, and associated fundamental mechanistic studies. We have focused our efforts on four classes of early metal alkyl complexes: (1) cationic group 4 Cp{sub 2}M(R){sup +} complexes (1) which are active species in Cp{sub 2}MX{sub 2}-based Ziegler-Natta olefin polymerization catalyst systems and which catalyze productive C-H activation reactions of heterocycles, (2) neutral (dicarbollide)(Cp*)M(R) complexes (2) which are structurally are electronically very similar to 1, (3) half-sandwich complexes CpM(R){sub 2}(L){sub n}{sup +} which are highly coordinatively and electronically unsaturated, and (4) new group 5 (dicarbollide)(Cp)MR{sub 2} and (dicarbollide){sub 2} MR complexes which are more unsaturated than group 5 Cp{sub 2}M systems due to incorporation of the dicarbollide ligand.

Jordan, R.F.

1991-01-01T23:59:59.000Z

289

Washing of field weathered crude oil contaminated soil with an environmentally compatible surfactant, alkyl polyglucoside  

Science Journals Connector (OSTI)

Weathered crude oil contaminated soils (COCSs), which are much more difficult to remediate than those freshly contaminated, are widespread especially at the sites of oil fields and industries. Surfactant enhanced ex situ soil washing could be used to remediate COCSs, but surfactant toxicity becomes one of the major concerns. In this study, a class of green surfactants, alkyl polyglucosides (APGs), were tested in washing the field weathered COCS with relatively high oil concentration (123 mg g?1 dry soil) from Jilin Oilfield, Northeastern China. APG1214, characterized with longer alkyl chain, was more effective than APG0810 in crude oil removal. Adding inorganic sodium salts into APG1214 solution further improved the crude oil removal efficiency (CORE). Washing parameters (temperature, washing time, agitation speed and solution/soil ratio) were investigated and further optimized integratedly with an orthogonal design. At the optimum conditions, the CORE reached 97%. GC/MS analysis showed that the proportion of small n-alkanes (C16–C23) in residual crude oil gradually increased, which was helpful to interpret the oil removal mechanism. Moreover, eminent effect on removal of large n-alkanes was achieved from the synergy between APG1214 and inorganic salts, which was opposite to the effect when they were added separately. This study demonstrated a promising way to remediate COCS with ecologically compatible surfactant and provided guidelines for its practical application.

Mei Han; Guodong Ji; Jinren Ni

2009-01-01T23:59:59.000Z

290

Nuclear magnetic resonance (N.M.R.) studies of alkyl formates and of alcohol-water azeotropes  

E-Print Network (OSTI)

from Eq. 2 for 12 Alkyl Formates in Carbon tetrachloride at 37'. Typical N. M. R. Spectrum of a Non-Azeotropic Ethanol- Water Mixture . 16 N. M. R. Spectrum Occasionally Found for Azeotropic Ethanol-Water Mixtures 17 PART I. ALKYL FORMATES... CHAPTER I. INTRODUCTION 1 It has been shown that eq. 1 applies almost exactly to the data for the alkaline hydrolysis of 9 acetate eaters (CH COOR ) in 40% 0 aqueous p - dioxane at 35 . In eq. 1, k is the second-order rate log k = l. 35 + 0. 688 o + 0...

O'Brien, Patrick William

2012-06-07T23:59:59.000Z

291

High-Octane Fuel from Refinery Exhaust Gas: Upgrading Refinery Off-Gas to High-Octane Alkylate  

SciTech Connect

Broad Funding Opportunity Announcement Project: Exelus is developing a method to convert olefins from oil refinery exhaust gas into alkylate, a clean-burning, high-octane component of gasoline. Traditionally, olefins must be separated from exhaust before they can be converted into another source of useful fuel. Exelus’ process uses catalysts that convert the olefin to alkylate without first separating it from the exhaust. The ability to turn up to 50% of exhaust directly into gasoline blends could result in an additional 46 million gallons of gasoline in the U.S. each year.

None

2009-12-01T23:59:59.000Z

292

Hydrocarbon concentrations at the Alpine mountain sites Jungfraujoch and Arosa  

Science Journals Connector (OSTI)

Volatile hydrocarbons have been measured for 1 yr at Arosa (2010 m asl) to determine the contribution of European emissions to the trace gas concentrations at this remote site. Results are compared to concurrent hydrocarbon concentrations at the high Alpine background site Jungfraujoch (3580 m asl). Hydrocarbon concentrations at Arosa are generally much higher than at Jungfraujoch. The influence of the Alpine boundary layer air was studied based on the diurnal variation of hydrocarbon concentrations, i.e. rising pollutant concentrations in the morning at Arosa and in the afternoon at Jungfraujoch. Different hydrocarbon emission sources of the uplifting air were found at the two sites. At Jungfraujoch, several transatlantic events were detected from October 2001 to January 2002 based on analysis of hydrocarbon ratios and air parcel trajectories. The OH concentration during the transatlantic transport was estimated to be around 5×105 cm?3, derived from simultaneous hydrocarbon oxidation and dilution in the free troposphere. These transatlantic transport events were tracked back to warm conveyor belts, characterized by uniform dynamics and relatively uniform surface sources. In addition, ozone production in the free tropospheric transport was also documented in these events.

Yingshi Li; Mike Campana; Stefan Reimann; Daniel Schaub; Konrad Stemmler; Johannes Staehelin; Thomas Peter

2005-01-01T23:59:59.000Z

293

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.

294

Iraq`s significant hydrocarbon potential remains relatively undeveloped  

SciTech Connect

Iraq is probably one of the least explored countries in the Middle East, despite the fact that it possesses one of the richest hydrocarbon basins in the world almost on a par to Saudi Arabia`s potential, if not more. The aim of this article is to state the facts about Iraq and focus on the huge but untapped and undeveloped hydrocarbon resources to the international oil community. Perhaps it is best to start by describing briefly the sedimentary and tectonic elements responsible for accumulating such large hydrocarbon resources. The paper describes the basin, tectonic elements, structural anomalies, deep drilling, source rocks, reservoir rocks, characteristics, and new reserves.

AL-Gailani, M. [GeoDesign Ltd., Kingston-upon-Thames (United Kingdom)

1996-07-29T23:59:59.000Z

295

Method for making hydrogen rich gas from hydrocarbon fuel  

DOE Patents (OSTI)

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

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

1999-07-27T23:59:59.000Z

296

Method for making hydrogen rich gas from hydrocarbon fuel  

DOE Patents (OSTI)

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

Krumpelt, Michael (Naperville, IL); Ahmed, Shabbir (Bolingbrook, IL); Kumar, Romesh (Naperville, IL); Doshi, Rajiv (Downers Grove, IL)

1999-01-01T23:59:59.000Z

297

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

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

emission Search Powered by Explorit Topic List Advanced Search Sample search results for: aromatic hydrocarbon emission...

298

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

E-Print Network (OSTI)

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

Dennis, J A

1971-01-01T23:59:59.000Z

299

Aniline-induced nitrosative stress in rat spleen: Proteomic identification of nitrated proteins  

SciTech Connect

Aniline exposure is associated with toxicity to the spleen which is characterized by splenomegaly, hyperplasia, fibrosis, and a variety of sarcomas on chronic exposure in rats. However, mechanisms by which aniline elicits splenotoxic responses are not well understood. Earlier we have shown that aniline exposure leads to increased nitration of proteins in the spleen. However, nitrated proteins remain to be characterized. Therefore, in the current study using proteomic approaches, we focused on characterizing the nitrated proteins in the spleen of aniline-exposed rats. Aniline exposure led to increased tyrosine nitration of proteins, as determined by 2D Western blotting with anti-3-nitrotyrosine specific antibody, compared to the controls. The analyzed nitrated proteins were found in the molecular weight range of 27.7 to 123.6 kDa. A total of 37 nitrated proteins were identified in aniline-treated and control spleens. Among them, 25 were found only in aniline-treated rats, 11 were present in both aniline-treated and control rats, while one was found in controls only. The nitrated proteins identified mainly represent skeletal proteins, chaperones, ferric iron transporter, enzymes, nucleic acids binding protein, and signaling and protein synthesis pathways. Furthermore, aniline exposure led to significantly increased iNOS mRNA and protein expression in the spleen, suggesting its role in increased reactive nitrogen species formation and contribution to increased nitrated proteins. The identified nitrated proteins provide a global map to further investigate alterations in their structural and functional properties, which will lead to a better understanding of the role of protein nitration in aniline-mediated splenic toxicity. - Highlights: > Proteomic approaches are used to identify nitrated proteins in the spleen. > Twenty five nitrated proteins were found only in the spleen of aniline-treated rats. > Aniline exposure led to increased iNOS mRNA and protein expression in the spleen. > Results support the role of nitrosative stress in splenic toxicity of aniline.

Fan Xiuzhen; Wang Jianling [Department of Pathology, University of Texas Medical Branch, Galveston, TX 77555 (United States); Soman, Kizhake V. [Department of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX 77555 (United States); Ansari, G.A.S. [Department of Pathology, University of Texas Medical Branch, Galveston, TX 77555 (United States); Department of Biochemistry and Molecular Biology, University of Texas Medical Branch, Galveston, TX 77555 (United States); Khan, M. Firoze, E-mail: mfkhan@utmb.edu [Department of Pathology, University of Texas Medical Branch, Galveston, TX 77555 (United States)

2011-08-15T23:59:59.000Z

300

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

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


301

Carbon?Oxygen Bond Forming Mechanisms in Rhenium Oxo-Alkyl Complexes  

SciTech Connect

Three C?X bond formation mechanisms observed in the oxidation of (HBpz{sub 3})ReO(R)(OTf) [HBpz{sub 3} = hydrotris(1-pyrazolyl)borate; R = Me, Et, and iPr; OTf = OSO{sub 2}CF{sub 3}] by dimethyl sulfoxide (DMSO) were investigated using quantum mechanics (M06//B3LYP DFT) combined with solvation (using the PBF Poisson?Boltzmann polarizable continuum solvent model). For R = Et we find the alkyl group is activated through ?-hydrogen abstraction by external base OTf{sup ?} with a free energy barrier of only 12.0 kcal/mol, leading to formation of acetaldehyde. Alternatively, ethyl migration across the M?O bond (leading to the formation of acetaldehyde and ethanol) poses a free energy barrier of 22.1 kcal/mol, and the previously proposed ?-hydrogen transfer to oxo (a 2+2 forbidden reaction) poses a barrier of 44.9 kcal/mol. The rate-determining step to formation of the final product acetaldehyde is an oxygen atom transfer from DMSO to the ethylidene, with a free energy barrier of 15.3 kcal/mol. When R = iPr, the alkyl 1,2-migration pathway becomes the more favorable pathway (both kinetically and thermodynamically), with a free energy barrier (?G{sup ?} = 11.8 kcal/mol) lower than ?-hydrogen abstraction by OTf{sup ?} (?G{sup ?} = 13.5 kcal/mol). This suggests the feasibility of utilizing this type of migration to functionalize M?R to M?OR. We also considered the nucleophilic attack of water and ammonia on the Re-ethylidene ?-carbon as a means of recovering two-electron-oxidized products from an alkane oxidation. Nucleophilic attack (with internal deprotonation of the nucleophile) is exothermic. However, the subsequent protonolysis of the Re?alkyl bond (to liberate an alcohol or amine) poses a barrier of 37.0 or 42.4 kcal/mol, respectively. Where comparisons are possible, calculated free energies agree very well with experimental measurements.

Cheng, Mu-Jeng; Nielsen, Robert J; Ahlquist, Marten; Goddard, William A

2010-01-01T23:59:59.000Z

302

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:

303

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

304

Temporary Anion States of Polyatomic Hydrocarbons KENNETH D. JORDAN'  

E-Print Network (OSTI)

Temporary Anion States of Polyatomic Hydrocarbons KENNETH D. JORDAN' OSpemnenr Of C%sITIkby. M k I. A biographyand photograph of Kenneth D. Jordan appear In previous paper in this issue. far outweighsthat

Simons, Jack

305

Biodegradability of select polycyclic aromatic hydrocarbon (pah) mixtures  

E-Print Network (OSTI)

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

Desai, Anuradha M.

2007-04-25T23:59:59.000Z

306

Experiments on Hydrocarbon Gas Hydrates in Unconsolidated Sand  

Science Journals Connector (OSTI)

Experiments were carried out to observe the formation and decomposition of hydrocarbon gas hydrates in an unconsolidated sand pack 4.4 cm in diameter and ... 43 bars and 5 to 10°C; gas used was 90% methane and 10...

P. E. Baker

1974-01-01T23:59:59.000Z

307

Filtration Combustion in Hydrocarbon Desorption from a Porous Medium  

Science Journals Connector (OSTI)

We have investigated theoretically and experimentally the process of filtration combustion with hydrocarbon desorption from a porous skeleton realized, in particular, in heat cleaning of porous media out of resid...

S. I. Fut'ko; K. V. Dobrego; E. S. Shmelev…

2003-11-01T23:59:59.000Z

308

Fireball during combustion of hydrocarbon fueld releases II. Thermal radiation  

Science Journals Connector (OSTI)

The processes of radiative heat transfer in a fireball which develops upon ignition of a cloud of hydrocarbon fuel near the Earth’s surface are simulated numerically. The emissive characteristics of combustion pr...

G. M. Makhviladze; J. P. Roberts; S. E. Yakush

309

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

310

Effect of the Composition of Hydrocarbon Streams on HCCI Performance  

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

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

311

Hydrocarbon pollution control and remediation of groundwater: a brief review  

Science Journals Connector (OSTI)

...oil-contaminated sediments. There are two main remediation techniques: soil washing and bio- remediation. With soil washing, contaminated soil is leached with water containing a surfactant to assist in hydrocarbon removal. In situ washing is undertaken...

L. Clark

312

THE HEATS OF COMBUSTION OF AROMATIC HYDROCARBONS AND HEXAMETHYLENE.  

Science Journals Connector (OSTI)

THE HEATS OF COMBUSTION OF AROMATIC HYDROCARBONS AND HEXAMETHYLENE. ... Citation data is made available by participants in CrossRef's Cited-by Linking service. ... Experimental methods included adiabatic heat-capacity calorimetry (5 K to 420 K), comparative ... ...

Theodore W. Richards; Frederick Barry

1915-01-01T23:59:59.000Z

313

Measurements of dissolved nonmethane hydrocarbons in sea water  

Science Journals Connector (OSTI)

An automated stripping technique for the measurement of dissolved hydrocarbons in sea water is presented together with some results obtained ... cruise from Europe to Brazil. The sea water concentrations of NMHC ...

C. Plass; R. Koppmann; J. Rudolph

314

Hygienic rating of hydrocarbons in bottom deposits of water ecosystems  

Science Journals Connector (OSTI)

The authors of this article draw the reader’s attention to the topical problem of the contamination of bottom deposits of water ecosystems by hydrocarbons, such as oil and gas condensate,...

Rauf Valievich Galiulin…

2014-05-01T23:59:59.000Z

315

E-Print Network 3.0 - aqueous magnesium nitrate Sample Search...  

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

in aqueous-phase atmospheric aerosols from... , a fundamental understanding of nitrate ions at the ... Source: Allen, Heather C.- Department of Chemistry, Ohio State University...

316

E-Print Network 3.0 - aqueous nitrate flowsheet Sample Search...  

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

in aqueous-phase atmospheric aerosols from... , a fundamental understanding of nitrate ions at the ... Source: Allen, Heather C.- Department of Chemistry, Ohio State University...

317

E-Print Network 3.0 - ammonium nitrate aerosols Sample Search...  

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

ON MINERAL DUSTS: CRYSTALLINE OR AQUEOUS? Summary: 02138, USA Keywords: Phase transition; Atmospheric Aerosols; Ammonium sulfate; Ammonium nitrate... that of ammonium...

318

E-Print Network 3.0 - aqueous nitrate solutions Sample Search...  

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

Biology and Medicine 23 Evaluation for Biological Reduction of Nitrate and Perchlorate in Brine Water Using Summary: in high salt solution. One culture was capable of reducing up...

319

E-Print Network 3.0 - ammonium nitrates Sample Search Results  

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

an electron acceptor... production, but when either ... Source: Collection: Renewable Energy ; Energy Storage, Conversion and Utilization 10 Nitrate accumulation Ammonium nitrogen...

320

E-Print Network 3.0 - alkaline nitrate solutions Sample Search...  

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

2010 www.atmos-chem-phys.net1039992010 Summary: . The model in- cludes explicit transport of size-resolved mineral dust and its alkalinity, nitrate... in terms of...

Note: This page contains sample records for the topic "hydrocarbons alkyl nitrates" 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

E-Print Network 3.0 - anaerobic nitrate-dependent oxidation Sample...  

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

of the experiment... nitrate- dependent Fe(II) ... Source: Roden, Eric E. - Department of Geology and Geophysics, University of Wisconsin at Madison Collection: Environmental...

322

Alkyl Chain Ordering of Asymmetric Phosphatidylcholines Adsorbed at a Liquid-Liquid B. L. Smiley and G. L. Richmond*  

E-Print Network (OSTI)

Alkyl Chain Ordering of Asymmetric Phosphatidylcholines Adsorbed at a Liquid-Liquid Interface B. L chain ordering in phosphatidylcholines (PCs) adsorbed from aqueous solution to a carbon tetrachloride-dimensional phases are discussed. Introduction Surfactant monolayers adsorbed at oil-water interfaces in biological

Richmond, Geraldine L.

323

Reductive Alkylation of Thioamides with Grignard Reagents in the Presence of Ti(OiPr)4: Insight and Extension  

Science Journals Connector (OSTI)

The reductive alkylation of thioamides by Grignard reagents in the presence of Ti(OiPr)4 is the subject of a study involving 20 different substrates. The influence of various parameters has been evaluated, showing notably that the yields of this ...

Fabien Hermant; Ewelina Urba?ska; Sarah Seizilles de Mazancourt; Thomas Maubert; Emmanuel Nicolas; Yvan Six

2014-07-28T23:59:59.000Z

324

The Absorption Spectra of Ethylene, Deutero-Ethylene and Some Alkyl-Substituted Ethylenes in the Vacuum Ultra-Violet  

Science Journals Connector (OSTI)

1 February 1940 research-article The Absorption Spectra of Ethylene, Deutero-Ethylene and Some Alkyl-Substituted Ethylenes in the Vacuum Ultra-Violet W. C. Price W. T. Tutte The Royal Society is collaborating with JSTOR to digitize...

1940-01-01T23:59:59.000Z

325

Reactions of r-Nucleophiles with Alkyl Chlorides: Competition between SN2 and E2 Mechanisms and the  

E-Print Network (OSTI)

Reactions of r-Nucleophiles with Alkyl Chlorides: Competition between SN2 and E2 Mechanisms (SN2) and base-induced elimination (E2). As the extent of substitution in the neutral reactants through a traditional SN2 transition state, followed by an elimination step in the SN2 product ion

Lineberger, W. Carl

326

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

327

Conversion of methane and acetylene into gasoline range hydrocarbons  

E-Print Network (OSTI)

CONVERSION OF METHANE AND ACETYLENE INTO GASOLINE RANGE HYDROCARBONS A Thesis by AMMAR ALKHAWALDEH Submitted to the Office of Graduate Studies of Texas A&M University in partial fulfillment of the requirements for the degree of MASTER... OF SCIENCE May 2000 Major Subject: Chemical Engineering CONVERSION OF METHANE AND ACETYLENE INTO GASOLINE RANGE HYDROCARBONS A Thesis by AMMAR ALKHAWALDEH Submitted to the Office of Graduate Studies of Texas A&M University in partial fulfillment...

Alkhawaldeh, Ammar

2012-06-07T23:59:59.000Z

328

Low severity hydrocarbon steam reforming process  

SciTech Connect

A process is described for producing ammonia which comprises: (a) primary catalytically reforming at super atmospheric pressure in a direct-fired primary reforming zone, a hydrocarbon feedstock with steam to produce a gas containing carbon oxides, hydrogen and methane; (b) secondary catalytically reforming the gas from step (a) by introducing air and bringing the mixture towards equilibrium thereby producing a secondary reformer effluent gas containing nitrogen, carbon oxides, hydrogen and a decreased quantity of methane; (c) converting carbon monoxide catalytically with steam to carbon dioxide and hydrogen; (d) removing carbon oxides to give an ammonia synthesis gas comprising nitrogen and hydrogen and compressing the gas to ammonia synthesis pressure; (e) reacting the synthesis gas in an ammonia synthesis zone to produce ammonia and recovering ammonia from the reacted gas to produce an ammonia-depleted gas stream; (f) recycling at least a portion of the ammonia-depleted gas stream to the ammonia synthesis zone; and (g) treating a sidestream of the ammonia-depleted gas to separate a stream enriched in hydrogen and an inerts-enriched gas stream, and returning the enriched hydrogen stream to the ammonia synthesis zone.

Osman, R.M.; Byington, R.G.

1986-06-03T23:59:59.000Z

329

Emission of polycyclic aromatic hydrocarbons in China  

SciTech Connect

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

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

2006-02-01T23:59:59.000Z

330

Rock types, pore types, and hydrocarbon exploration  

SciTech Connect

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

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

1985-05-01T23:59:59.000Z

331

energy savings by the use of mtbe to replace alkylate in automotive gasolines  

SciTech Connect

This paper presents data on the differences in energy consumption in the production of leaded and unleaded AI-93 gasolines with various blend components. The authors investigate as high-octane components certain products that are more effective in use and less energy-consuming in production in comparison with alkylate. In particular, methyl tert-butyl ether (MTBE) is discussed; it is not poisonous, it has a high heat of combustion, and it does not attack materials of construction. The addition of 11% MTBE to gasoline lowers the cold start temperature of engines by 10-12 degrees. Moreover, no adjustment of the carburetor is required for the changeover to gasoline with 11% MTBE.

Englin, B.A.; Emel'yanov, V.E.; Terent'ev, G.A.; Vinogradov, A.M.

1986-07-01T23:59:59.000Z

332

A preliminary evaluation model for reservoir hydrocarbon-generating potential established based on dissolved hydrocarbons in oilfield water  

Science Journals Connector (OSTI)

A large number of oilfield water samples were analyzed in this work. Research ... relationship between the concentrations and distribution of dissolved hydrocarbons suggested that the contents and composition of ...

Hongjing Zhao; Weilin Sun; Baotian He; Bowen Mei…

2006-01-01T23:59:59.000Z

333

Raman Scattering Sensor for Control of the Acid Alkylation Process in Gasoline Production  

SciTech Connect

Gasoline refineries utilize a process called acid alkylation to increase the octane rating of blended gasoline, and this is the single most expensive process in the refinery. For process efficiency and safety reasons, the sulfuric acid can only be used while it is in the concentration range of 98 to 86 %. The conventional technique to monitor the acid concentration is time consuming and is typically conducted only a few times per day. This results in running higher acid concentrations than they would like to ensure that the process proceeds uninterrupted. Maintaining an excessively high acid concentration costs the refineries millions of dollars each year. Using SBIR funding, Process Instruments Inc. has developed an inline sensor for real time monitoring of acid concentrations in gasoline refinery alkylation units. Real time data was then collected over time from the instrument and its responses were matched up with the laboratory analysis. A model was then developed to correlate the laboratory acid values to the Raman signal that is transmitted back to the instrument from the process stream. The instrument was then used to demonstrate that it could create real-time predictions of the acid concentrations. The results from this test showed that the instrument could accurately predict the acid concentrations to within ~0.15% acid strength, and this level of prediction proved to be similar or better then the laboratory analysis. By utilizing a sensor for process monitoring the most economic acid concentrations can be maintained. A single smaller refinery (50,000 barrels/day) estimates that they should save over $120,000/year, with larger refineries saving considerably more.

Uibel, Rory, H.; Smith, Lee M.; Benner, Robert, E.

2006-04-19T23:59:59.000Z

334

Stereoselective SN2? alkylation reaction sequence of the ?,?-epoxy ?,?-unsaturated ester system via ?,?-chlorohydrin intermediates by the use of a R3Al–CuCN reagent  

Science Journals Connector (OSTI)

A novel stereoselective SN2? alkylation reaction sequence of the ?,?-epoxy ?,?-unsaturated ester system has been developed which involves a regioselective substitution reaction with chloride ions at the ?-position and a subsequent SN2? alkylation reaction of the resulting ?-chloro-?-hydroxy derivatives with a R3Al–CuCN reagent. The new methodology was demonstrated to be applicable to a variety of substrates and to provide various ?-hydroxy-?-alkyl-?,?-unsaturated esters including those bearing a quaternary asymmetric carbon atom at the ?-position in a highly stereoselective manner and high yields.

Fumihiko Yoshimura; Atsushi Matsui; Atsushi Hirai; Keiji Tanino; Masaaki Miyashita

2009-01-01T23:59:59.000Z

335

Kidney cancer and hydrocarbon exposures among petroleum refinery workers  

SciTech Connect

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

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

1993-12-01T23:59:59.000Z

336

Correction to ``Nitrate and colloid transport through coarse Hanford sediments under steady state,  

E-Print Network (OSTI)

Correction to ``Nitrate and colloid transport through coarse Hanford sediments under steady state), Correction to ``Nitrate and colloid transport through coarse Hanford sediments under steady state, variably and colloid transport through coarse Hanford sediments under steady state, variably saturated flow'' by Kelly

Flury, Markus

337

Dietary inorganic nitrate reverses features of metabolic syndrome in endothelial nitric oxide synthase-deficient mice  

Science Journals Connector (OSTI)

...mitochondria to affect oxygen consumption, substrate oxidation, and generation...that dietary nitrate fuels a nitrate-nitrite-NO...libitum. Water and food consumption were determined...microreaction purge vessel coupled with a condenser...integrated with the purge vessel and the outlet of the...

Mattias Carlström; Filip J. Larsen; Thomas Nyström; Michael Hezel; Sara Borniquel; Eddie Weitzberg; Jon O. Lundberg

2010-01-01T23:59:59.000Z

338

J. Phycol. 38, 971982 (2002) FIELD ASSAYS FOR MEASURING NITRATE REDUCTASE ACTIVITY IN ENTEROMORPHA SP.  

E-Print Network (OSTI)

and subsequent storage at 80 C preserved NR activity and allowed for later laboratory use of the optimized.; nitrate reductase; macroalgae; Mobile Bay; Ulva sp. Abbreviation: ASW, artificial seawater; FSW, filtered seawater; NR, nitrate reductase Macroalgal production is frequently limited by the availability

Sherman, Tim

339

Nitrate-responsive miR393/AFB3 regulatory module controls root system architecture in  

E-Print Network (OSTI)

environmental conditions is the modulation of root system architecture (RSA) in response to nitrate supplyNitrate-responsive miR393/AFB3 regulatory module controls root system architecture in ArabidopsisR393/AFB3 is a unique N- responsive module that controls root system architecture in response

Green, Pamela

340

Stainless steel corrosion by molten nitrates : analysis and lessons learned.  

SciTech Connect

A secondary containment vessel, made of stainless 316, failed due to severe nitrate salt corrosion. Corrosion was in the form of pitting was observed during high temperature, chemical stability experiments. Optical microscopy, scanning electron microscopy and energy dispersive spectroscopy were all used to diagnose the cause of the failure. Failure was caused by potassium oxide that crept into the gap between the primary vessel (alumina) and the stainless steel vessel. Molten nitrate solar salt (89% KNO{sub 3}, 11% NaNO{sub 3} by weight) was used during chemical stability experiments, with an oxygen cover gas, at a salt temperature of 350-700 C. Nitrate salt was primarily contained in an alumina vessel; however salt crept into the gap between the alumina and 316 stainless steel. Corrosion occurred over a period of approximately 2000 hours, with the end result of full wall penetration through the stainless steel vessel; see Figures 1 and 2 for images of the corrosion damage to the vessel. Wall thickness was 0.0625 inches, which, based on previous data, should have been adequate to avoid corrosion-induced failure while in direct contact with salt temperature at 677 C (0.081-inch/year). Salt temperatures exceeding 650 C lasted for approximately 14 days. However, previous corrosion data was performed with air as the cover gas. High temperature combined with an oxygen cover gas obviously drove corrosion rates to a much higher value. Corrosion resulted in the form of uniform pitting. Based on SEM and EDS data, pits contained primarily potassium oxide and potassium chromate, reinforcing the link between oxides and severe corrosion. In addition to the pitting corrosion, a large blister formed on the side wall, which was mainly composed of potassium, chromium and oxygen. All data indicated that corrosion initiated internally and moved outward. There was no evidence of intergranular corrosion nor were there any indication of fast pathways along grain boundaries. Much of the pitting occurred near welds; however this was the hottest region in the chamber. Pitting was observed up to two inches above the weld, indicating independence from weld effects.

Kruizenga, Alan Michael

2011-09-01T23:59:59.000Z

Note: This page contains sample records for the topic "hydrocarbons alkyl nitrates" 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

Corrosion of Iron Stainless Steels in Molten Nitrate Salt  

Science Journals Connector (OSTI)

Abstract Energy storage for concentrating solar power (CSP) is a major area of research that seeks to lower the levelized cost of electricity within the aggressive SunShot goals of 6¢/kW-hrth[1–3]. One viable approach is sensible thermal energy storage (TES), which currently utilizes molten nitrate binary salt, stored at 575 °C in the hot tank of a two tank system [4,5]. Increasing the temperature limit within the hot tank requires a detailed understanding of materials corrosion behavior, in addition to salt thermal stability properties. High temperature nickel based alloys are the logical choice for strength and corrosion resistance as elevated temperatures will increase corrosion kinetics, however, the cost of nickel based alloys are nearly four times more expensive than iron based steels [6]. For this reason iron based stainless steels, specifically 321SS and 347SS (nominally Fe-17Cr-9Ni), were chosen for investigation at several temperatures in nitrate salt. 316SS, an elementally similar alloy, was susceptible to stress corrosion cracking while tested at Solar Two [4]. It was suggested that alloys with stabilizing additions of niobium (347SS) or titanium (321SS) would mitigate this deleterious behavior. Flat coupon samples were immersed in binary nitrate salts at temperatures of 400, 500, 600, and 680 °C, with air sparging on all tests. Samples were nominally removed at intervals of 500, 1000, 2000, and 3000 hours to acquire data on time varying weight gain information while simultaneously employing metallography to identify corrosion mechanisms occurring within the melt. Corrosion rates varied dramatically with temperature according to an Arrhenius-type behavior. 347SS and 321SS had very little oxidation for 400 and 500 °C, indicative of a protective corrosion scale and low corrosion kinetics. Data at 600 °C showed that 321SS tended toward linear oxidation behavior based on oxide spallation which was observed on the samples upon removal. Corrosion products at 500 °C had phases of iron oxide, with obvious chromium depletion as observed in energy dispersive spectroscopy (EDS) scans. 600 °C corrosion layers were primarily iron oxide with obvious phases of sodium ferrite on the outer surface. 680 °C marked an excessive rate of corrosion with metal loss in both alloys.

Alan Kruizenga; David Gill

2014-01-01T23:59:59.000Z

342

In Situ Hydrocarbon Degradation by Indigenous Nearshore Bacterial Populations  

SciTech Connect

Potential episodic hydrocarbon inputs associated with oil mining and transportation together with chronic introduction of hydrocarbons via urban runoff into the relatively pristine coastal Florida waters poses a significant threat to Florida's fragile marine environment. It is therefore important to understand the extent to which indigenous bacterial populations are able to degrade hydrocarbon compounds and also determine factors that could potentially control and promote the rate at which these compounds are broken down in situ. Previous controlled laboratory experiments carried out by our research group demonstrated that separately both photo-oxidation and cometabolism stimulate bacterial hydrocarbon degradation by natural bacterial assemblages collected from a chronically petroleum contaminated site in Bayboro Bay, Florida. Additionally, we also demonstrated that stable carbon and radiocarbon abundances of respired CO{sub 2} could be used to trace in situ hydrocarbon degradation by indigenous bacterial populations at this same site. This current proposal had two main objectives: (a) to evaluate the cumulative impact of cometabolism and photo-oxidation on hydrocarbon degradation by natural bacterial assemblages collected the same site in Bayboro Bay, Florida and (b) to determine if in situ hydrocarbon degradation by indigenous bacterial populations this site could be traced using natural radiocarbon and stable carbon abundances of assimilated bacterial carbon. Funds were used for 2 years of full support for one ESI Ph.D. student, April Croxton. To address our first objective a series of closed system bacterial incubations were carried out using photo-oxidized petroleum and pinfish (i.e. cometabolite). Bacterial production of CO{sub 2} was used as the indicator of hydrocarbon degradation and {delta}{sup 13}C analysis of the resultant CO{sub 2} was used to evaluate the source of the respired CO{sub 2} (i.e. petroleum hydrocarbons or the pinfish cometabolite). Results from these time series experiments demonstrated that short-term exposure of petroleum to UV light enhanced hydrocarbon degradation by 48% over that observed for non-photo-oxidized petroleum. Despite the greater bio-availability of the photo-oxidized over the non-photo-oxidized petroleum, an initial lag in CO{sub 2} production was observed indicating potential phototoxicity of the photo- by-products. {delta}{sup 13}C analysis and mass balance calculations reveal that co-metabolism with pinfish resulted in increased hydrocarbon degradation for both photo-oxidized and non-photo-oxidized petroleum each by over 100%. These results demonstrate the cumulative effect of photo-oxidation and co-metabolism on petroleum hydrocarbon degradation by natural bacterial populations indigenous to systems chronically impacted by hydrocarbon input. To address the second objective of this proposal bacterial concentrates were collected from Bayboro Harbor in April 2001 for nucleic acid extraction and subsequent natural radiocarbon abundance analyses. Unfortunately, however, all of these samples were lost due to a faulty compressor in our -70 freezer. The freezer was subsequently repaired and samples were again collected from Bayboro Harbor in June 2002 and again December 2002. Several attempts were made to extract the nucleic acid samples--however, the student was not able to successfully extract and an adequate amount of uncontaminated nucleic acid samples for subsequent natural radiocarbon abundance measurements of the bacterial carbon by accelerator mass spectrometry (i.e. require at least 50 {micro}g carbon for AMS measurement). Consequently, we were not able to address the second objective of this proposed work.

Cherrier, J.

2005-05-16T23:59:59.000Z

343

Preliminary assessment of hydrocarbon potential in southern Illinois  

SciTech Connect

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

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

1989-08-01T23:59:59.000Z

344

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

345

Analysis of Enriched Uranyl Nitrate in Nested Annular Tank Array  

SciTech Connect

Two series of experiments were performed at the Rocky Flats Critical Mass Laboratory during the 1980s using highly enriched (93%) uranyl nitrate solution in annular tanks. [1, 2] Tanks were of typical sizes found in nuclear production plants. Experiments looked at tanks of varying radii in a co-located set of nested tanks, a 1 by 2 array, and a 1 by 3 array. The co-located set of tanks had been analyzed previously [3] as a benchmark for inclusion within the International Handbook of Evaluated Criticality Safety Benchmark Experiments. [4] The current study represents the benchmark analysis of the 1 by 3 array of a series of nested annular tanks. Of the seventeen configurations performed in this set of experiments, twelve were evaluated and nine were judged as acceptable benchmarks.

John D. Bess; James D. Cleaver

2009-06-01T23:59:59.000Z

346

Studies on the reverse osmosis treatment of uranyl nitrate solution  

SciTech Connect

The aqueous effluent generated in uranium processing, particularly in the nuclear fuel fabrication step, contains mainly uranium nitrate. This requires treatment before discharge into the environment to meet stringent standards. This paper presents the performance of cellulose acetate membranes with regard to rejection of uranium under reverse osmotic conditions for feed concentrations up to 200 mg/l of uranium, which corresponds to the levels normally prevalent in the effluents. The use of additives like the disodium salt of ethylenediaminetetraacetic acid and sodium sulfate for the improvement of reverse osmosis performance of the above membranes was also investigated. In the light of the experimental results, the suitability of reverse osmosis for the decontamination of uranium effluents is discussed.

Prabhakar, S.; Panicker, S.T.; Misra, B.M.; Ramani, P.S. (Bhabha Atomic Research Centre, Bombay (India))

1992-03-01T23:59:59.000Z

347

Role of Nitrate in Conditioning Aquifer Sediments for Technetium Bioreduction  

Science Journals Connector (OSTI)

Earth System Science Institute, School of Earth and Environment, University of Leeds, Leeds, LS2 9JT, U.K., Williamson Research Centre for Molecular Environmental Science, School of Earth, Atmospheric and Environmental Sciences, The University of Manchester, Manchester, M13 9PL, U.K., and Centre for Radiochemistry Research, The University of Manchester, Manchester, M13 9PL, U.K. ... These results have implications for Tc-cycling in contaminated environments where nitrate has been considered undesirable, but where it may enhance Fe(III)-reduction via a novel pH “conditioning” step. ... Wilkins, M. J.; Livens, F. R.; Vaughan, D. J.; Beadle, I.; Lloyd, J. R. The influence of microbial redox cycling on radionuclide mobility in the subsurface at a low-level radioactive waste storage site Geobiology 2007, 5, 293– 301 ...

Gareth T. W. Law; Andrea Geissler; Christopher Boothman; Ian T. Burke; Francis R. Livens; Jonathan R. Lloyd; Katherine Morris

2009-11-10T23:59:59.000Z

348

FUMIGATION, GROSS NITROGEN TRANSFORMATIONS, N-15, NITRATE, RATES, SOIL  

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

FUMIGATION, GROSS NITROGEN TRANSFORMATIONS, N-15, FUMIGATION, GROSS NITROGEN TRANSFORMATIONS, N-15, NITRATE, RATES, SOIL 1909 Pushnik, J.C., R.S. Demaree, J.L.J. Houpis, W.B. Flory, S.M. Bauer, and P.D. Anderson. 1995. The effect of elevated carbon dioxide on a Sierra-Nevadan dominant species: Pinus ponderosa. Journal of Biogeography 22(2-3):249-254. The impact of increasing atmospheric CO2 has not been fully evaluated on western coniferous forest species. Two year old seedlings of Pinus ponderosa were grown in environmentally controlled chambers under increased CO2 conditions (525 mu L L(-1) and 700 mu L L(-1)) for 6 months. These trees exhibited morphological, physiological and biochemical alterations when compared to our controls (350 mu L L(- 1)). Analysis of whole plant biomass distribution has shown no

349

13C NMR Investigation of the Chemical Structures of Coking and Non-Coking Coals in the Original and Reductively Alkylated Solid States  

Science Journals Connector (OSTI)

Chemical structures of four Turkish coals in their original and reductively alkylated forms were investigated in the solid state by13C NMR, using cross polarization and magic-angle spinning. Changes in13C NMR int...

Gaye Erbatur; Oktay Erbatur; Abdullah Coban; Mark F. Davis…

1984-01-01T23:59:59.000Z

350

Selective and quantitative nitrate electroreduction to ammonium using a porous copper electrode in an electrochemical flow cell  

E-Print Network (OSTI)

,version1-10Jul2014 #12;3 1. Introduction Nitrate ions (NO3 - ) contamination of ground and surface water and physiochemical methods are used for nitrate removal from contaminated water but show drastic limits are costly [10] and produce secondary brine wastes, because the nitrate are only separated but not destroyed

Paris-Sud XI, Université de

351

Determination of Polycyclic Aromatic Hydrocarbons in Fresh Milk by Hollow Fiber Liquid-Phase Microextraction–Gas Chromatography Mass Spectrometry  

Science Journals Connector (OSTI)

......Polycyclic Aromatic Hydrocarbons in Fresh Milk by...polycyclic aromatic hydrocarbons (PAHs) in fresh...more volatile and heat sensitive. The...Polycyclic aromatic hydrocarbons (PAHs) are compounds...the incomplete combustion of carbon-containing...respectively. Data were collected......

Mohd Marsin Sanagi; Saw Hong Loh; Wan Aini Wan Ibrahim; Mohamed Noor Hasan; Hassan Y. Aboul Enein

2013-02-01T23:59:59.000Z

352

Hepatic coenzyme Q redox balance of fishes as a potential bioindicator of environmental contamination by polycyclic aromatic hydrocarbons  

Science Journals Connector (OSTI)

...at the land-water interface are...polycyclic aromatic hydrocarbon (PAH) contamination...Markers 0 Polycyclic Hydrocarbons, Aromatic 0 Water Pollutants, Chemical...metabolism Polycyclic Hydrocarbons, Aromatic toxicity...Ubiquinone metabolism Water Pollutants, Chemical...

2011-01-01T23:59:59.000Z

353

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

354

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. 4 figs.

Kong, P.C.; Lessing, P.A.

1995-06-27T23:59:59.000Z

355

Hydrocarbon composition of crude oil from Lam Bank  

SciTech Connect

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

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

1987-07-01T23:59:59.000Z

356

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

357

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

358

Method for determining processability of a hydrocarbon containing feedstock  

SciTech Connect

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

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

2013-09-10T23:59:59.000Z

359

Upgrading of petroleum oil feedstocks using alkali metals and hydrocarbons  

DOE Patents (OSTI)

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

Gordon, John Howard

2014-09-09T23:59:59.000Z

360

Isoconversional Kinetic Analysis of the Combustion of Heavy Hydrocarbons  

Science Journals Connector (OSTI)

One method to access unconventional, heavy-oil resources as well as waterflood residual oil is to apply in situ combustion (ISC) to oxidize in place a small fraction of the hydrocarbon, thereby providing heat to reduce oil viscosity and pressure that enhances recovery. ... As shown by Vyazovkin,(12) these deviations of temperature yield erroneous values of activation energy, when such a data set is used with a model that assumes linear heating. ... Estimates were made of the heat produced, and a formula was derived for computing the heat of combustion of hydrocarbons in the high-temp. ...

Murat Cinar; Louis M. Castanier; Anthony R. Kovscek

2009-07-06T23:59:59.000Z

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


361

Application of municipal sludge (biosolids) for agricultural purposes and groundwater nitrate concentrations  

SciTech Connect

One of the more popular means of handling sewage sludge from municipalities is its application to agricultural lands. A variety of crops are grown with the expectation that plants will utilize the nitrogen. However, a complex scenario allows some of the nitrate to move below root depth and eventually to the water table at depths of up to 30 ft. The City of Raleigh, NC injects sewage sludge ( residuals'', biosolids'') into soils derived largely from the Rolesville Granite in an area of typical rolling Piedmont topography. A 1975 background study of part of the site demonstrated differences in groundwater quality between areas farmed over a period of years and areas dominated by second-growth pine and harwood forests. Groundwater quality data collected semiannually between 1982 and 1988 show gradual buildup of nitrate in some fields; in others groundwater quality apparently remains unaffected by nitrate from the sludge. Monitoring well placement may play a role in these differences. Minimum time from the sludge application to an increase in groundwater nitrate is from 9 to 12 months. An ongoing study of a 12-acre field which lay fallow for a number of years prior to sludge application in 1990 demonstrates that some nitrate does move downward fairly rapidly, its movement being recorded in both the saprolite and groundwater. Comparison of nitrate content of groundwater from monitoring wells at a nearby dairy farm shows that normal agricultural practices may also increase the nitrate content of the shallow groundwater.

Welby, C.W. (North Carolina State Univ., Raleigh, NC (United States). Dept. of Marine, Earth and Atmospheric Sciences)

1993-03-01T23:59:59.000Z

362

In-situ remediation of nitrate-contaminated ground water by electrokinetics/iron wall processes  

Science Journals Connector (OSTI)

The feasibility of using electrokinetics coupled with a zero valent iron (Fe0) treatment wall to abiotically remediate nitrate-contaminated soils was investigated. Upon completion of each test run, the contaminated soil specimen was sliced into five parts and analyzed for nitrate-nitrogen, ammonia-nitrogen and nitrite-nitrogen. Nitrogen mass balance was used to determine the major transformation products. In control experiments where only electrokinetics was used at various constant voltages, 25 to 37% of the nitrate-nitrogen was transformed. The amount of nitrate-nitrogen transformed improved when a Fe0 wall (20 g or about 8–10% by weight) was placed near the anode. For test runs at various constant voltages, the amount of nitrate-nitrogen transformed ranged from 54 to 87%. By switching to constant currents, the amount of nitrate-nitrogen — transformed was about 84 to 88%. The major transformation products were ammonia-nitrogen and nitrogen gases. Nitrite-nitrogen was less than 1% in all experimental runs. Two localized pH conditions exist in the system, a low pH region near the anode and a high pH region near the cathode. Placing of an iron wall near the anode increases the pH in that area as time increases. Movement of the acid front did not flush across the cathode. This research has demonstrated that the electrokinetics/iron wall process can be used to remediate nitrate-contaminated groundwater.

Chin F. Chew; Tian C. Zhang

1998-01-01T23:59:59.000Z

363

Experimental and artificial neural network modeling study on soot formation in premixed hydrocarbon flamesq  

E-Print Network (OSTI)

Experimental and artificial neural network modeling study on soot formation in premixed hydrocarbon after the methane flames, respectively. Three-layer, feed- forward type artificial neural networks rights reserved. Keywords: Soot; Hydrocarbon flames; Artificial neural networks 1. Introduction

Senkan, Selim M.

364

The Fate of Fossil Fuel Hydrocarbons in Marine Animals [and Discussion  

Science Journals Connector (OSTI)

20 May 1975 research-article The Fate of Fossil Fuel Hydrocarbons in Marine Animals [and Discussion] E...have been made of their fate in mammals. The fate of fossil fuel hydrocarbons in marine animals. | Journal Article...

1975-01-01T23:59:59.000Z

365

Bioenergy Technologies Office Conversion R&D Pathway: Syngas Upgrading to Hydrocarbon Fuels  

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

Syngas upgrading to hydrocarbon fuels is one of eight priority pathways chosen to convert biomass into hydrocarbon fuels by the Bioenergy Technologies Office. These pathways were down-selected from an initial list of 18.

366

Dynamic study of coupled heavy hydrocarbon pyrolysis and combustion. N. Gascoina*  

E-Print Network (OSTI)

1/28 Dynamic study of coupled heavy hydrocarbon pyrolysis and combustion. N. Gascoina* , P of the heat transfer dynamics. Finally, the combustion mechanism is applied and validated experimentally for kerosene pyrolysis application. Keywords Regenerative cooling; Hydrocarbon pyrolysis; Supersonic Combustion

Boyer, Edmond

367

The Energies of the Atomic Linkages in the Normal Paraffin Hydrocarbons  

Science Journals Connector (OSTI)

...normal paraffin hydrocarbons, in the gaseous...values for the heats of combustion of these gases...values for the heats of combustion of the hydrocarbon gases,4'5...Jessup4 on the heats of combustion of normal heptane...

Frederick D. Rossini

1934-01-01T23:59:59.000Z

368

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

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

various hydrocarbons on monolithic hydrocarbon adsorber Dae Jung Kim,a Ji Man Kim,a Jae Eui Yie... ,b, Seong Gyu Seo,c and Sang-Chai Kim d a Department of Molecular Science and...

369

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

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

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

370

Vibration Spectra of Hydrocarbon Molecules. II. Skeletal Frequencies in Certain Branched Paraffins  

Science Journals Connector (OSTI)

25 October 1949 research-article Vibration Spectra of Hydrocarbon Molecules. II...characteristic frequencies should be assigned as vibrations of the carbon skeleton of these structural...problem of the interpretation of the vibration spectra of hydrocarbons is considered...

1949-01-01T23:59:59.000Z

371

Environmental and Transport Effects on Core Measurements of Water Saturation, Salinity, Wettability, and Hydrocarbon Composition  

E-Print Network (OSTI)

and core surfacing operations can significantly alter the water saturation, salinity, hydrocarbon measurements of water saturation, salinity, hydrocarbon composition, and wettability are critical for accurateSPE 166154 Environmental and Transport Effects on Core Measurements of Water Saturation, Salinity

Torres-Verdín, Carlos

372

Light hydrocarbons in the surface water of the mid-Atlantic  

Science Journals Connector (OSTI)

During a cruise of RV Polarstern over the Atlantic in September/October 1988, C2?C4 hydrocarbons were measured in surface sea water. The ship passed through three different ocean ... at 8° N and 3° S. Hydrocarbon

C. Plass; R. Koppmann; J. Rudolph

1992-11-01T23:59:59.000Z

373

Extraction of carbonate complexes of trivalent transplutonium elements with alkyl pyrocatechols  

SciTech Connect

Extraction of trivalent americium curium, californium, and europium with a technical mixture of mono-and didecyl pyrocatechols (TAP) in different diluents from carbonate solutions is studied. The influence of various factors (pH, K/sub 2/CO/sub 3/, TAP and metal concentration, phase contact time) on the degree of extraction and separation of the elements is clarified. It is shown that the elements concerned are extracted quantitatively by TAP solution in toluene and cyclohexane in the K/sub 2/CO/sub 3/ concentration range 0.25-1.5 M. A difference is noted in the coefficients of americium and curium distribution when they are extracted with TAP from 0.25 M K/sub 2/CO/sub 3/ solution. The separation coefficients of this pair rise with the pH of the carbonate solution. The separation coefficients of this pair rise with the pH of the carbonate solution. The separation can be improved at the stage of reextraction of the elements with a mixture of K/sub 2/CO/sub 3/ and DTPA or EDTA from alkyl pyrocatechol because the americium and curium reextraction rate constants differ widely. The composition of the compounds in the organic phase based on 4-(..cap alpha..,..cap alpha..-dioctylethyl)pyrocatechol (DOP) is studied by /sup 13/C NMR spectroscopy.

Karalova, Z.K.; Bukina, T.I.; Myasoedov, B.F.; Fedorov, L.A.; Sokolovskii, S.A.

1987-01-01T23:59:59.000Z

374

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

E-Print Network (OSTI)

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

375

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

E-Print Network (OSTI)

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

Mazzini, Adriano

376

The Interaction of Carcinogenic Hydrocarbons with Tissues VII. Fractionation of Mouse Skin Proteins  

Science Journals Connector (OSTI)

...Inferaction of Hydrocarbons with Tissues. VII...separation of the water- soluble proteins...in Chart 1, and water-soluble proteins...Interaction of Hydrocarbons with Tissues. VII...noncarcinogenic hydrocarbons could be detected...electrophoretic separation of water-soluble proteins...

G. Rodman Davenport; C. W. Abell; and Charles Heidelberger

1961-06-01T23:59:59.000Z

377

Male-derived cuticular hydrocarbons signal sperm competition intensity and affect ejaculate expenditure in crickets  

Science Journals Connector (OSTI)

...taxa has shown that cuticular hydrocarbons (CHCs), contact pheromones...They were supplied with water and fed cat food ad libitum...between-family variation in male hydrocarbon profiles (Thomas Simmons...variation within the blends of hydrocarbons in this experiment, male...

2009-01-01T23:59:59.000Z

378

Speciation and Quantitation of Hydrocarbons in Gasoline Engine Exhaust  

Science Journals Connector (OSTI)

......laboratory engines or reactors. In this paper we...computer technology have advanced to the state where...2-1 m), and the heavy (C5 -C1 2 ) hydrocarbons...PLOT column with water or heavy hy drocarbons...technology to prevent water vapor from condensing...computer technology have advanced to the state where......

Keith L. Olson; Robert M. Sinkevitch; Thompson M. Sloane

1992-12-01T23:59:59.000Z

379

Hydrocarbon Condensation in Heavy-Duty Diesel Exhaust  

Science Journals Connector (OSTI)

Hydrocarbon Condensation in Heavy-Duty Diesel Exhaust ... The semivolatile mass fraction of diesel exhaust particles was studied using size-resolved on-line techniques (DMA-ELPI; TDMA-ELPI). ... The measured size resolved values of mass transfer imply that condensation, or diffusion-limited mass transfer, plays a major role in driving the volatile matter to the diesel exhaust particles. ...

Jyrki Ristimäki; Kati Vaaraslahti; Maija Lappi; Jorma Keskinen

2007-08-10T23:59:59.000Z

380

High Levels of Carcinogenic Polycyclic Aromatic Hydrocarbons in Mate Drinks  

Science Journals Connector (OSTI)

...leaves and/or exposure to combustion products or formation of ash...analysis of the mainstream smoke chemistry of samples of the U.S. cigarette...comparison of the tumors induced by coal tar and benzo[a]pyrene...Spectrometry Ilex paraguariensis chemistry Polycyclic Hydrocarbons, Aromatic...

Farin Kamangar; Michele M. Schantz; Christian C. Abnet; Renato B. Fagundes; and Sanford M. Dawsey

2008-05-01T23:59:59.000Z

Note: This page contains sample records for the topic "hydrocarbons alkyl nitrates" 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

Seismic Analysis Using Wavelet Transform for Hydrocarbon Detection  

E-Print Network (OSTI)

data quality is good. This technique can be directly applied to the processed 2D and 3 D pre-stack/post-stack data sets (1) to detect hydrocarbon zones in both clastic and carbonate reservoirs by analyzing the low frequency signals in the decomposed...

Cai, Rui

2012-02-14T23:59:59.000Z

382

Chemical Kinetics of Hydrocarbon Ignition in Practical Combustion Systems  

SciTech Connect

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

Westbrook, C.K.

2000-07-07T23:59:59.000Z

383

Energy Conservation Opportunities in Hydrocarbon Resin Manufacturing Facilities  

E-Print Network (OSTI)

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

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

384

Fundamental spectroscopic studies of carbenes and hydrocarbon radicals  

SciTech Connect

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

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

1993-12-01T23:59:59.000Z

385

Climatically driven emissions of hydrocarbons from marine sediments during deglaciation  

Science Journals Connector (OSTI)

...destabilizing hydrates shown in the lighter...destabilization of methane hydrates and release of...in SBC suggest gas emissions during...investigate the sand-sized fraction...the presence of sand layers (23...hydrocarbons and methane hydrate, which is widely...4) (24). Gas hydrates commonly...

T. M. Hill; J. P. Kennett; D. L. Valentine; Z. Yang; C. M. Reddy; R. K. Nelson; R. J. Behl; C. Robert; L. Beaufort

2006-01-01T23:59:59.000Z

386

Hydrocarbons Heterogeneous Pyrolysis: Experiments and Modeling for Scramjet Thermal Management  

E-Print Network (OSTI)

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

Paris-Sud XI, Université de

387

Hydrocarbon saturation determination using acoustic velocities obtained through casing  

DOE Patents (OSTI)

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

Moos, Daniel (Houston, TX)

2010-03-09T23:59:59.000Z

388

Increased olefins production via recovery of refinery gas hydrocarbons  

SciTech Connect

In the process of catalytically cracking heavy petroleum fractions to make gasoline and light fuel oil, by-product waste gases are also generated. The waste gases, normally used as fuel, are themselves rich sources of ethylene, propylene and other light hydrocarbons which can be recovered inexpensively via a cryogenic dephlegmator process. This gas separation technique is exploited in a system, in operation since spring of 1987, which reclaims C/sub 2/+ hydrocarbons from a refinery gas. The reclamation process bolsters production in a nearby ethylene plant. Causing no disruption of ethylene plant operations, the cryogenic hydrocarbon recovery system functions smoothly with existing systems. The dephlegmation unit operation melds distillation and heat transfer processes in a single easily-controlled step which boosts the hydrocarbon purity and recovery above the levels profitably achievable with conventional cryogenic separation techniques. Very attractive operating economics follow from high purity, high recovery, and high energy efficiency. This paper discusses process concepts, economic benefits, plant operation, and early performance results.

Bernhard, D.P.; Rowles, H.C.; Moss, J.A.; Pickering, J.L. Jr.

1988-01-01T23:59:59.000Z

389

THERMOCATALYTIC CO2-FREE PRODUCTION OF HYDROGEN FROM HYDROCARBON FUELS  

E-Print Network (OSTI)

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

390

Biodegradation of total petroleum hydrocarbon (TPH) in Jordanian petroleum sludge  

Science Journals Connector (OSTI)

Bioremediation, or the use of micro-organisms to decontaminate soil or groundwater, is being increasingly seen as an effective, environment-friendly treatment for oil-contaminated sites. In this study, the results are presented concerning a laboratory screening of several natural bacterial consortia and laboratory tests to establish the performance in degradation of hydrocarbons contained in oily sludge from the Jordan Oil Refinery Plant. As a result of the laboratory screening, 18 isolates were selected and grouped into two main clusters; cluster 1 containing 12 isolates grown at 43°C, and cluster 2 containing six isolates grown at 37°C. Three natural bacterial consortia with ability to degrade total petroleum hydrocarbons (TPH) were prepared from these isolates. Experiments were conducted in Erlenmeyer flasks under aerobic conditions, with TPH removal percentage varying from 5.9% to 25.1%, depending upon consortia type and concentration. Consortia 7B and 13B exhibited the highest TPH removal percentages of 25% and 23%, respectively before nutrient addition. TPH removal rate was enhanced after addition of nutrients to incubated flasks. The highest TPH reduction (37%) was estimated after addition of a combination of nitrogen, phosphorus and sulphur to consortia 7B. This is the first report concerning biological treatment of total petroleum hydrocarbon by bacteria isolated from the oil refinery plant, where it lay the ground for full integrated studies recommended for hydrocarbon degradation that assist in solving sludge problems.

Bassam Mrayyan; Mohammad Battikhi

2004-01-01T23:59:59.000Z

391

Hydrocarbons in rift basins: the role of stratigraphy  

Science Journals Connector (OSTI)

...succession that causes the shales to reach thermal maturity and generate hydrocarbons. Simple...T. J. 1988 Rift basins of interior Sudan--petroleum exploration and discovery...basins? Is that what we could call the thermal subsidence phase? J. J. Lambiase...

1999-01-01T23:59:59.000Z

392

Application of Resource-Ratio Theory to Hydrocarbon Biodegradation  

Science Journals Connector (OSTI)

Application of Resource-Ratio Theory to Hydrocarbon Biodegradation ... We suggest that the procedures outlined here can be used to help guide practical decisions about the nutrients that are most likely to be growth-limiting and help define the subsequent nutrient application rates. ...

Val H. Smith; David W. Graham; Dale D. Cleland

1998-09-12T23:59:59.000Z

393

Theoretical studies of hydrocarbon combustion chemistry. Annual progress report  

SciTech Connect

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

Schaefer, H.F. III

1994-08-01T23:59:59.000Z

394

FROM INTERSTELLAR POLYCYCLIC AROMATIC HYDROCARBONS AND ICE TO ASTROBIOLOGY  

E-Print Network (OSTI)

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

395

Degradation of Polycyclic Aromatic Hydrocarbons at Low Temperature under Aerobic and Nitrate-Reducing Conditions in Enrichment Cultures from Northern Soils  

Science Journals Connector (OSTI)

...incineration, storage, or soil washing (12). PAHs are often found in oil spills and in soil at old gasworks sites...H. Frimmel. 1997. Surfactant-enhanced mobilization...manufactured gas. Plant Soil Environ. Sci. Technol...

Mikael Eriksson; Erik Sodersten; Zhongtang Yu; Gunnel Dalhammar; William W. Mohn

2003-01-01T23:59:59.000Z

396

On the Chemla effect in molten alkali nitrates  

Science Journals Connector (OSTI)

The Chemla effect concerns the strong composition dependence of the internal ionic mobilities of cations in mixtures of two molten salts with a common anion in which the mobility of the large cation can be higher than the small one at low concentrations of the latter. Molecular dynamics simulations of molten ( Li Cs)NO 3 ( Li K)NO 3 ( Li Na)NO 3 ( Na Cs)NO 3 each at two different compositions at a given temperature and also pure LiNO 3 and pure KNO 3 have been performed with the aim of reproducing the Chemla effect. The key role played by anion polarization on the Chemla effect in molten alkali nitrates is demonstrated by comparing the calculated mobilities using nonpolarizable and polarizable models. Polarization effects were included in the simulations by using a previously proposed fluctuating charge model (FCM) for the NO 3 ? anion. It is shown that a single potential model for a ( M 1 M 2 ) NO 3 mixture gives the correct composition dependence of the M 1 and the M 2 mobilities provided that polarization effects are included in the model. The FCM is thus transferable between different systems but not its nonpolarizable counterpart. Structure and dynamics of the simulated systems are discussed in light of proposed models for the Chemla effect.

Mauro C. C. Ribeiro

2002-01-01T23:59:59.000Z

397

Development of electrochemical denitrification from waste water containing ammonium nitrate  

SciTech Connect

The authors developed processes to dentrify waste water containing ammonium nitrate discharged from the nuclear fuel manufacturing works and to recover nitric acid and ammonia. For denitrification they applied the operating method and the conditions of operation to make 0.4mM or less from NH{sub 4}NO{sub 3} waste water of 1.5 M by 3 stages of electrodialysis cells. To recover nitric acid and ammonium water, they separated HNO{sub 3} solution of 6 M and NH{sub 4}OH solution with one unit of electrolysis cell, then absorbed NH{sub 3} gas from NH{sub 4}OH solution with water and applied the condition of operation to recover 8 M NH{sub 4}OH solution. The authors demonstrated that treatment and recovery can be carried out stably with actual waste water with a system through the combination of previously mentioned electrodialysis cells, electrolysis cells and an ammonia gas absorber. At present they are planning a plant where NH{sub 4}NO{sub 3} waste water of 4,500 mol can be treated per day.

Sawa, Toshio; Hirose, Yasuo; Ishii, Yoshinori; Takatsudo, Atsushi; Wakasugi, Kazuhico; Hayashi, Hiroshi

1995-12-31T23:59:59.000Z

398

Hugoniot and Shock Initiation Studies of Isopropyl Nitrate  

Science Journals Connector (OSTI)

Isopropyl nitrate (IPN) is a liquid explosive of rather low energy. We have measured the sound speed and used it in the universal liquid Hugoniot to produce an estimated Hugoniot for this material. Gas?gun?driven multiple?magnetic?gauge measurements were made to measure a Hugoniot state at 6 GPa; it was in good agreement with the prediction. Two similar experiments were conducted at higher pressure inputs to study the shock?to?detonation transition in IPN; the high inputs required for initiation necessitated the use of a two?stage gun. One experiment with an input of 9.0 GPa into the IPN produced a run to detonation of about 3 mm and the in?situ particle velocity profiles showed the expected homogeneous initiation behavior of a growing wave behind the shock front that overtakes the front and decays to a steady detonation. The reactive wave in the shocked IPN appears to have achieved a steady superdetonation in both of the initiation experiments. This is the first time a steady superdetonation has been measured with in?situ gauges.

S. A. Sheffield; L. L. Davis; M. R. Baer; Ray Engelke; R. R. Alcon; A. M. Renlund

2002-01-01T23:59:59.000Z

399

Hugoniot and shock initiation studies of isopropyl nitrate  

SciTech Connect

Isopropyl nitrate (IPN) is a liquid explosive of rather low energy. We have measured the sound speed and used it in the universal liquid Hugoniot to produce an estimated Hugoniot for this material. Gas-gun-driven, multiple-magnetic-gauge measurements were made to measure a Hugoniot state at 6 GPa; it was in good agreement with the prediction. Two similar experiments were conducted at higher pressure inputs to study the shock-to-detonation transition in IPN; the high inputs required for initiation necessitated the use of a two-stage gun. One experiment with an input of 9.0 GPa into the IPN produced a run to detonation of about 3 mm and the in-situ particle velocity profiles showed the expected homogeneous initiation behavior of a growing wave behind the shock front that overtakes the front and decays to a steady detonation. The reactive wave in the shocked IPN appears to have achieved a steady superdetonation in both of the initiation experiments. This is the first time a steady superdetonation has been measured with in-situ gauges.

Sheffield, S. A. (Stephen A.); Davis, L. L. (Lloyd L.); Baer, M. R. (Mel R.); Engelke, R. P. (Raymond P.); Alcon, R. R. (Robert R.); Renlund, Anita Mariana

2001-01-01T23:59:59.000Z

400

SunShot Initiative: Advanced Nitrate Salt Central Receiver Power Plant  

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

Advanced Nitrate Salt Central Receiver Power Plant Advanced Nitrate Salt Central Receiver Power Plant Abengoa logo Photo of two lit towers surrounded by much smaller blue flat plates that are mounted on the ground. Commercial central receiver plant designs Abengoa, under the Baseload CSP FOA, will demonstrate a 100-megawatt electrical (MWe) central receiver plant using nitrate salt as the receiver coolant, thermal storage medium, and heat transport fluid in the steam generator. Approach The plan is to operate the plant at full load for 6,400 hours each year using only solar energy. Abengoa is working to create a team of suppliers capable of deploying a commercially ready nitrate salt central receiver technology that can be competitive in the current power marketplace. Innovation Abengoa is developing a new molten-salt power tower technology with a surround heliostat field. Key components include:

Note: This page contains sample records for the topic "hydrocarbons alkyl nitrates" 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

A Conceptual Nitrate Transport Model and Its Application at Different Scales  

Science Journals Connector (OSTI)

Liu et al. [12...] reported the calibration of a diffuse nitrate model (the DNMT model) at White Cart Water Catchment against the observed water quality...K 0 (the hydraulic conductivity at grou...

Shuming Liu; Peter Tucker; Martin Mansell

2010-08-01T23:59:59.000Z

402

Spring-neap modulation of internal tide mixing and vertical nitrate ...  

Science Journals Connector (OSTI)

Sep 1, 2007 ... Measurements of the intra-tidal and spring–neap variation in the vertical flux of nitrate into ... ultimately dissipates the energy of the internal tide.

2007-08-13T23:59:59.000Z

403

Ethylene oxidation by lithium nitrate in the presence of palladium acetate in acetic acid  

Science Journals Connector (OSTI)

Data are reported on variations of the gas phase volume and product accumulation in ethylene oxidation by lithium nitrate in acetic acid solutions, catalyzed by palladium acetate. An assumption is made on the rou...

N. I. Kuznetsova; A. F. Danilyuk…

404

Water purification of nitrates by low-pressure reverse osmosis method  

Science Journals Connector (OSTI)

The paper has investigated possibilities and basic regularities of water purification of nitrates by low pressure reverse osmosis. The negative influence of chlorides and sulfates ... made on expediency of using ...

V. V. Goncharuk; V. O. Osipenko…

2013-03-01T23:59:59.000Z

405

Sodium-Copper Exchange on Wyoming Montmorillonite in Chloride, Perchlorate, Nitrate, and Sulfate Solutions  

E-Print Network (OSTI)

Sodium-Copper Exchange on Wyoming Montmorillonite in Chloride, Perchlorate, Nitrate, and Sulfate. The copper exchange capacity (CuEC) and Na-Cu exchange reactions on Wyoming montmo- rillonite were studied

Sparks, Donald L.

406

Application of Artificially Immobilized Microorganisms to Nitrate Removal from Drinking Water  

E-Print Network (OSTI)

to Nitrate Removal from Drinking Water By Sean X. Liu andFor biological treatment of drinking water, several crucialalginate gel beads to drinking water treatment has proved to

Liu, Sean X; Hermanowicz, Slawomir W

1997-01-01T23:59:59.000Z

407

Reclamation and groundwater remediation at a hydrocarbon site in Alaska  

SciTech Connect

As part of a joint hydrocarbon cleanup project between Unocal and Marathon, we have initiated the use of constructed wetlands for restoration of the 40-acre Poppy Lane gravel pit located near Kenai, Alaska. Gravel excavated from this site was used to construct roads and drilling pads in the 1960`-70`s. During this period it was also used as a refuse dump for waste from the Kenai gas field and from local residents. The bulk wastes were removed and pockets of oily sand were removed, treated and returned to a stockpile on the site. This left the site with residual pockets of hydrocarbon-impacted sand (<1000 TPH) plus traces of hydrocarbon contamination in the uppermost shallow groundwater flowing through the outwash gravels. The final part of the cleanup will be land restoration and bioremediation of the final traces of hydrocarbons, which are predominantly diesel-range. High resolution gas chromatography analysis indicated that common plants already growing on the site (willow, cottonwood, and alder) did not concentrate diesel-range petroleum hydrocarbons in their foliage when growing in soils containing these contaminants. As part of the planned restoration and shallow groundwater remediation, two 1/3 acre test plots were constructed to promote in-situ biodegradation processes. In spring 1995, the first test, a tree root-barrier plot, was planted with dormant cuttings of four native wetland tree and shrub species, which were planted to depths up to five feet. Alder and elderberry did not succeed under any conditions, nor did any species planted in standing water. For cottonwood and willow species, approximately one half of each rooted and survived. When the water table dropped the second year, the willow cuttings rooted deeper in the vadose zone, while cottonwood did not. As a result of these findings, a tree root-barrier wetland is not considered to be a viable option for groundwater treatment at Poppy Lane.

Ririe, G.T. [Unocal, Brea, CA (United States); Drake, L.D. [Univ. of Iowa, Iowa City, IA (United States); Olson, S.S. [Marathon Oil, Tyler, TX (United States)

1997-12-31T23:59:59.000Z

408

Interaction of Carcinogenic Hydrocarbons with Tissues: VIII. Binding of Tritium-labeled Hydrocarbons to the Soluble Proteins of Mouse Skin  

Science Journals Connector (OSTI)

...treated as described in "Materials and Methods." A demonstration...of the unbound radio active hydrocarbon was removed...migrated toward the cathode, a neutral in dicator...pro teins toward the cathode was affected by electro...dermis as described in "Materials and Methods." The...

C. W. Abell and Charles Heidelberger

1962-09-01T23:59:59.000Z

409

Herbicide and nitrate distribution in central Iowa rainfall  

SciTech Connect

Herbicides are detected in rainfall; however, these are a small fraction of the total applied. This study was designed to evaluate monthly and annual variation in atrazine (6-chloro-N-ethyl-N{prime}-(1-methylethyl)-1,3,5-triazine-2,4-diamine), alachlor (2-chloro-N-(2,6-diethylphenyl)-N-(methoxymethyl)acetamide), metolachlor (2-chloro-N-(2-ethyl-6-methylphenyl)-N-(2-methoxy-1-methylethyl)acetamide), and NO{sub 3}-N concentrations in rainfall over Walnut Creek watershed south of Ames, IA. The study began in 1991 and continued through 1994. Within the watershed, two wet/dry precipitation samplers were positioned 4 km apart. Detections varied during the year with >90% of the herbicide detections occurring in April through early July. Concentrations varied among events from nondetectable amounts to concentrations of 154 {mu}g L{sup {minus}1}, which occurred when atrazine was applied during an extremely humid day immediately followed by rainfall of <10 mm that washed spray drift from the atmosphere. This was a local scale phenomenon, because the other collector had a more typical concentration of 1.7 {mu}g L{sup {minus}1} with an 8-mm rainfall. VAriation between the two collectors suggests that local scale meteorological processes affect herbicide movement. Yearly atrazine deposition totals were >100 {mu}g m{sup {minus}2} representing <0.1% of the amount applied. Nitrate-N concentrations in precipitation were uniformly distributed throughout the year and without annual variation in the concentrations. Deposition rates of NO{sub 3}-N were about 1.2 g m{sup {minus}2}. Annual loading onto the watershed was about 25% of the amount applied from all forms of N fertilizers. Movement and rates of deposition provide an understanding of the processes and magnitude of the impact of agriculture on the environment. 7 refs., 5 figs., 3 tabs.

Hatfield, J.L.; Prueger, J.H.; Pfeiffer, R.L. [National Soil Tilth Lab., Ames, IA (United States); Wesley, C.K. [Princeton Univ., NJ (United States)

1996-03-01T23:59:59.000Z

410

Nonmonotonic Electric Conductivity by Alkyl-chain Variation of an Ionic Additive in Percolated Nonionic W/O-Microemulsions  

Science Journals Connector (OSTI)

Nonmonotonic Electric Conductivity by Alkyl-chain Variation of an Ionic Additive in Percolated Nonionic W/O-Microemulsions ... Accordingly, we equate the electrochemical potentials of the anion in both phases Equation 1 is explicitly written, that is where eo, are the elementary charge, , the standard potentials of the anion in the respective states, , the anion concentrations at the interface and in the oil phase, and ?intf, and ?oil the electrical potentials of the interface and oil phases. ... The bilayers, which are here considered have shorter chain length but are interdigitated (if two nano-droplets approach each other) with a consequently considerable resistance regarding diffusion. ...

Hans-Friedrich Eicke

2001-03-13T23:59:59.000Z

411

Apparatus for removing hydrocarbon contaminants from solid materials  

DOE Patents (OSTI)

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

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

1996-01-01T23:59:59.000Z

412

Method for removing hydrocarbon contaminants from solid materials  

DOE Patents (OSTI)

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

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

1995-01-01T23:59:59.000Z

413

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

414

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

415

Impaired mitochondrial respiration and protein nitration in the rat hippocampus after acute inhalation of combustion smoke  

SciTech Connect

Survivors of massive inhalation of combustion smoke endure critical injuries, including lasting neurological complications. We have previously reported that acute inhalation of combustion smoke disrupts the nitric oxide homeostasis in the rat brain. In this study, we extend our findings and report that a 30-minute exposure of awake rats to ambient wood combustion smoke induces protein nitration in the rat hippocampus and that mitochondrial proteins are a sensitive nitration target in this setting. Mitochondria are central to energy metabolism and cellular signaling and are critical to proper cell function. Here, analyses of the mitochondrial proteome showed elevated protein nitration in the course of a 24-hour recovery following exposure to smoke. Mass spectrometry identification of several significantly nitrated mitochondrial proteins revealed diverse functions and involvement in central aspects of mitochondrial physiology. The nitrated proteins include the ubiquitous mitochondrial creatine kinase, F1-ATP synthase {alpha} subunit, dihydrolipoamide dehydrogenase (E3), succinate dehydrogenase Fp subunit, and voltage-dependent anion channel (VDAC1) protein. Furthermore, acute exposure to combustion smoke significantly compromised the respiratory capacity of hippocampal mitochondria. Importantly, elevated protein nitration and reduced mitochondrial respiration in the hippocampus persisted beyond the time required for restoration of normal oxygen and carboxyhemoglobin blood levels after the cessation of exposure to smoke. Thus, the time frame for intensification of the various smoke-induced effects differs between blood and brain tissues. Taken together, our findings suggest that nitration of essential mitochondrial proteins may contribute to the reduction in mitochondrial respiratory capacity and underlie, in part, the brain pathophysiology after acute inhalation of combustion smoke.

Lee, Heung M.; Reed, Jason; Greeley, George H. [Department of Surgery, University of Texas Medical Branch (United States); Englander, Ella W. [Department of Surgery, University of Texas Medical Branch (United States); Shriners Hospitals for Children, Galveston, TX (United States)], E-mail: elenglan@utmb.edu

2009-03-01T23:59:59.000Z

416

Uranyl nitrate-exposed rat alveolar macrophages cell death: Influence of superoxide anion and TNF ? mediators  

SciTech Connect

Uranium compounds are widely used in the nuclear fuel cycle, military and many other diverse industrial processes. Health risks associated with uranium exposure include nephrotoxicity, cancer, respiratory, and immune disorders. Macrophages present in body tissues are the main cell type involved in the internalization of uranium particles. To better understand the pathological effects associated with depleted uranium (DU) inhalation, we examined the metabolic activity, phagocytosis, genotoxicity and inflammation on DU-exposed rat alveolar macrophages (12.5–200 ?M). Stability and dissolution of DU could differ depending on the dissolvent and in turn alter its biological action. We dissolved DU in sodium bicarbonate (NaHCO{sub 3} 100 mM) and in what we consider a more physiological vehicle resembling human internal media: sodium chloride (NaCl 0.9%). We demonstrate that uranyl nitrate in NaCl solubilizes, enters the cell, and elicits its cytotoxic effect similarly to when it is diluted in NaHCO{sub 3}. We show that irrespective of the dissolvent employed, uranyl nitrate impairs cell metabolism, and at low doses induces both phagocytosis and generation of superoxide anion (O{sub 2}{sup ?}). At high doses it provokes the secretion of TNF? and through all the range of doses tested, apoptosis. We herein suggest that at DU low doses O{sub 2}{sup ?} may act as the principal mediator of DNA damage while at higher doses the signaling pathway mediated by O{sub 2}{sup ?} may be blocked, prevailing damage to DNA by the TNF? route. The study of macrophage functions after uranyl nitrate treatment could provide insights into the pathophysiology of uranium?related diseases. -- Highlights: ? Uranyl nitrate effect on cultured macrophages is linked to the doses and independent of its solubility. ? At low doses uranyl nitrate induces generation of superoxide anion. ? At high doses uranyl nitrate provokes secretion of TNF?. ? Uranyl nitrate induces apoptosis through all the range of doses tested.

Orona, N.S. [School of Science and Technology, National University of General Martín, Avda Gral Paz 5445 (1650) San Martín, Buenos Aires (Argentina)] [School of Science and Technology, National University of General Martín, Avda Gral Paz 5445 (1650) San Martín, Buenos Aires (Argentina); Tasat, D.R., E-mail: deborah.tasat@unsam.edu.ar [School of Science and Technology, National University of General Martín, Avda Gral Paz 5445 (1650) San Martín, Buenos Aires (Argentina); School of Dentistry, University of Buenos Aires, M. T. de Alvear 2142 (1122), Buenos Aires (Argentina)

2012-06-15T23:59:59.000Z

417

Faults as potential hydrocarbon barriers, Arroyo Grande, California  

E-Print Network (OSTI)

OPTICALMICROSCOPY. Composition. Grain Size Characteristics Deformation Fluorescence Observations . Microprobe Observations. CAPILLARY PRESSURE. Sample Preparation. Test Procedures. Interpretation of the Mercury Injection Capillary Pressure Curve... rim of hydrocarbons seen on the grains. 41 , , 42 25 Photomicrograph of one of the microcracks that contains oil, 43 26 Microprobe image of the zone of quartz cement seen in the quarry, 27 Mercury injection capillary pressure apparatus, 45 48...

Switek, Daniel Paul

2012-06-07T23:59:59.000Z

418

THE INFRARED SPECTROSCOPY OF NEUTRAL POLYCYCLIC AROMATIC HYDROCARBON CLUSTERS  

SciTech Connect

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

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

2013-10-10T23:59:59.000Z

419

Method and apparatus for production of subsea hydrocarbon formations  

DOE Patents (OSTI)

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

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

1992-01-01T23:59:59.000Z

420

Method and apparatus for production of subsea hydrocarbon formations  

DOE Patents (OSTI)

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

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

1994-01-01T23:59:59.000Z

Note: This page contains sample records for the topic "hydrocarbons alkyl nitrates" 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

Petroleum hydrocarbon-degrading bacteria in the Galveston Bay system  

E-Print Network (OSTI)

PETROLEUM HYDRQCARBOiV-DEGRADING BACTERIA IN THE GALVESTON BAY SYSTEM A Thesis by STEVEN JAMES SCHROPP Submitted to the Graduate College of Texas ASM University in partial fulfillment of the requirement for the degree of MASTER OF SCIFNCE... December 1979 Major Subject: Biology PETROLEUM HYDROCARBON-DEGRADING BACTERIA IN THE GALVESTON BAY SYSTEM A Thesis by STEVEN JAMES SCHROPP Approved as to style and content by: (Co-Chairman of Committee) '( ~CA. ( -Chairman of Committee) (Head...

Schropp, Steven James

1979-01-01T23:59:59.000Z

422

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

423

Direct production of fractionated and upgraded hydrocarbon fuels from biomass  

SciTech Connect

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

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

2014-08-26T23:59:59.000Z

424

Catalyst and process for steam-reforming of hydrocarbons  

SciTech Connect

An improved catalyst and an improved process for use of the catalyst in the steam-hydrocarbon reforming reaction are disclosed. The catalyst comprises a group VIII metal on a cylindrical ceramic support consisting essentially of alpha alumina and having a plurality of gas passages extending axially therethrough. These supported catalysts display a higher geometric surface area and a lower pressure drop than do standard rings.

Atwood, K.; Merriam, J.S.; Wright, J.H.

1980-11-11T23:59:59.000Z

425

Polycyclic aromatic hydrocarbon distributions in Mississippi Fan sediments  

E-Print Network (OSTI)

. Sandberg, B. A. , University of Colorado Chairman of Advisory Committee: Dr. James M. Brooks Polycyclic aromatic hydrocarbon (PAH) distributions in Upper Pleistocene sediments of the Mississippi Fan and two intraslope basins in the Gulf of Mexico... chemistries is separate phase migration driven by hydrodynamic flow upward along fault planes. The same variables at intraslope basin sites are highly altered, possibly due to extensive gravity slump faulting. High- performance liquid chromatography...

Sandberg, William Allan

2012-06-07T23:59:59.000Z

426

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

427

Irregular spacing of heat sources for treating hydrocarbon containing formations  

DOE Patents (OSTI)

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

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

2012-06-12T23:59:59.000Z

428

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

SciTech Connect

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

Carroll, Herbert B.; Johnson, William I.

1999-04-27T23:59:59.000Z

429

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

SciTech Connect

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

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

1991-06-01T23:59:59.000Z

430

Crystal chemistry of new thorium nitrates and chromates  

SciTech Connect

The structures and infrared spectra of six novel thorium compounds are reported. Th(NO{sub 3}){sub 2}(OH){sub 2}(H{sub 2}O){sub 2} (1) crystallizes in space group C2/c, a=14.050(1), b=8.992(7), c=5.954(5) Å, ?=101.014(2)°. K{sub 2}Th(NO{sub 3}){sub 6} (2), P-3, a=13.606(1), c=6.641(6) Å. (C{sub 12}H{sub 28}N){sub 2}Th(NO{sub 3}){sub 6} (3), P21/c, a=14.643(4), b=15.772(5), c=22.316(5) Å, ?=131.01(1)°. KTh(NO{sub 3}){sub 5}(H{sub 2}O){sub 2} (4), P21/c, a=10.070(8), b=12.731(9), c=13.231(8) Å, ?=128.647(4)°. Th(CrO{sub 4}){sub 2}(H{sub 2}O){sub 2} (5), P21/n, a=12.731(1), b=9.469(8), c=12.972(1) Å, ?=91.793(2)°. K{sub 2}Th{sub 3}(CrO{sub 4}){sub 7}(H{sub 2}O){sub 10} (6), Ama2, a=19.302(8), b=15.580(6), c=11.318(6) Å. The coordination polyhedra about Th in these structures are diverse. Th is coordinated by 9 O atoms in 5 and 6, seven of which are from monodentate (CrO{sub 4}) tetrahedra and two are (H{sub 2}O). The Th in compound 1 is coordinated by ten O atoms, four of which are O atoms of two bidentate (NO{sub 3}) triangles and six of which are (OH) and (H{sub 2}O). In compounds 2, 3 and 4 the Th is coordinate by 12 O atoms. In 2 and 3 there are six bidentate (NO{sub 3}) triangles, and in 4 ten of the O atoms are part of five bidentate (NO{sub 3}) triangles and the others are (H{sub 2}O) groups. The structural units of these compounds consist of a chain of thorium and nitrate polyhedra (1), isolated thorium hexanitrate clusters (2, 3), an isolated thorium pentanitrate dihydrate cluster (4), and a sheet (6) and framework (5) of thorium and chromate polyhedra. These structures illustrate the complexity inherent in the crystal chemistry of Th.

Sigmon, Ginger E.; Burns, Peter C

2010-01-01T23:59:59.000Z

431

Factors affecting the discharge lifetime of lithium-molten nitrate thermal battery cells using soluble cathode materials  

Science Journals Connector (OSTI)

The use of soluble cathode materials in molten nitrate electrolyte thermal battery cells presents several problems related to cathode...? rich separator layer.

G. E. McManis; A. N. Fletcher; M. H. Miles

1986-09-01T23:59:59.000Z

432

Synthesis and chemistry of cationic d{sup 0} metal alkyl complexes. Progress report, July 1988--May 1991  

SciTech Connect

The objective of this project is to develop new types of electrophilic metal alkyl complexes for catalytic C-H activation and olefin polymerization chemistry, and associated fundamental mechanistic studies. We have focused our efforts on four classes of early metal alkyl complexes: (1) cationic group 4 Cp{sub 2}M(R){sup +} complexes (1) which are active species in Cp{sub 2}MX{sub 2}-based Ziegler-Natta olefin polymerization catalyst systems and which catalyze productive C-H activation reactions of heterocycles, (2) neutral (dicarbollide)(Cp*)M(R) complexes (2) which are structurally are electronically very similar to 1, (3) half-sandwich complexes CpM(R){sub 2}(L){sub n}{sup +} which are highly coordinatively and electronically unsaturated, and (4) new group 5 (dicarbollide)(Cp)MR{sub 2} and (dicarbollide){sub 2} MR complexes which are more unsaturated than group 5 Cp{sub 2}M systems due to incorporation of the dicarbollide ligand.

Jordan, R.F.

1991-12-31T23:59:59.000Z

433

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

DOE Patents (OSTI)

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

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

2014-05-06T23:59:59.000Z

434

Low time resolution analysis of polar ice cores cannot detect impulsive nitrate events  

E-Print Network (OSTI)

Ice cores are archives of climate change and possibly large solar proton events (SPEs). Wolff et al. (2012) used a single event, a nitrate peak in the GISP2-H core, which McCracken et al. (2001a) time associated with the poorly quantified 1859 Carrington event, to discredit SPE-produced, impulsive nitrate deposition in polar ice. This is not the ideal test case. We critique the Wolff et al. analysis and demonstrate that the data they used cannot detect impulsive nitrate events because of resolution limitations. We suggest re-examination of the top of the Greenland ice sheet at key intervals over the last two millennia with attention to fine resolution and replicate sampling of multiple species. This will allow further insight into polar depositional processes on a sub-seasonal scale, including atmospheric sources, transport mechanisms to the ice sheet, post-depositional interactions, and a potential SPE association.

Smart, D F; Melott, A L; Laird, C M

2015-01-01T23:59:59.000Z

435

Apparatus and method for rapid separation and detection of hydrocarbon fractions in a fluid stream  

DOE Patents (OSTI)

An apparatus and method for rapid fractionation of hydrocarbon phases in a sample fluid stream are disclosed. Examples of the disclosed apparatus and method include an assembly of elements in fluid communication with one another including one or more valves and at least one sorbent chamber for removing certain classifications of hydrocarbons and detecting the remaining fractions using a detector. The respective ratios of hydrocarbons are determined by comparison with a non separated fluid stream.

Sluder, Charles S.; Storey, John M.; Lewis, Sr., Samuel A.

2013-01-22T23:59:59.000Z

436

A study of the structure of the hydrocarbons of primary hard-coal tar  

SciTech Connect

The hydrocarbons isolated from primary hard-coal (G/sub 6/ gas coal) tar have been investigated by a combination of physicochemical and chemical methods. It has been established that the hydrocarbons boiling up to 573 K are mainly aliphatic, hydroaromatic, and naphthenic and are aromatic only to a smaller degree. Molecular and presumable structural formulas of the oxygen compounds isolated from the 473-573 K hydrocarbon fraction have been derived.

Platonov, V.V.; Gerasimova, N.I.; Ivleva, L.N.; Klyavina, O.A.; Vishnyakov, S.N.

1985-01-01T23:59:59.000Z

437

Initiation Mechanisms and Kinetics of Pyrolysis and Combustion of JP-10 Hydrocarbon Jet Fuel  

Science Journals Connector (OSTI)

Initiation Mechanisms and Kinetics of Pyrolysis and Combustion of JP-10 Hydrocarbon Jet Fuel ... We found that the primary decomposition reactions involve either (1) dissociation of ethylene from JP-10, resulting in the formation of a C8 hydrocarbon intermediate, or (2) the production of two C5 hydrocarbons. ... Heats of combustion (kcal/mole) were measured via O bomb calorimetry; adamantane (I) (c), -1441.95 ...

Kimberly Chenoweth; Adri C. T. van Duin; Siddharth Dasgupta; William A. Goddard III

2009-02-11T23:59:59.000Z

438

Characterizing and Biological Monitoring of Polycyclic Aromatic Hydrocarbons in Exposures to Diesel Exhaust  

Science Journals Connector (OSTI)

Characterizing and Biological Monitoring of Polycyclic Aromatic Hydrocarbons in Exposures to Diesel Exhaust ... Diesel and Gasoline Engine Exhausts and Some Nitroarenes; IARC:? Lyon, France 1989. ...

Wei Huang; Thomas J. Smith; Long Ngo; Tong Wang; Hongqiao Chen; Fanggu Wu; Robert F. Herrick; David C. Christiani; Hui Ding

2007-03-16T23:59:59.000Z

439

Naphthenic/paraffinic hydrocarbons of residual lube stock from West Siberian crudes  

SciTech Connect

The lube stocks from West Siberian crudes are characterized by high contents of aromatic hydrocarbons and by high viscosity indexes of the naphthenic/paraffinic and aromatic hydrocarbons. Mass spectrometric analysis showed that isoparaffins account for one-third of the total naphthenic/paraffinic hydrocarbons. The study showed that the naphthenic/paraffinic hydrocarbons of the residual lube stock from West Siberia crudes, even with a variation of molecular weight over broad limits, are relatively uniform in composition. They consist mainly of isoparaffinic and monocyclic and noncondensed naphthenic structures.

Detusheva, E.P.; Bogdanov, Sh.K.; Khramtsova, L.P.; Nekrasova, A.V.; Shkol'nikov, V.M.

1983-03-01T23:59:59.000Z

440

E-Print Network 3.0 - abundant accessible hydrocarbons Sample...  

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

Functionalization: An Energy Frontier Research... such as hydrocarbons, dioxygen, water, carbon dioxide and dihydrogen are central to new technologies for the use... of...

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


441

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

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

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

442

Calculation of the heats of combustion of aromatic hydrocarbons contained in power-generating fuel  

Science Journals Connector (OSTI)

The additive method of group contributions is used for the calculation of the heats of combustion of aromatic hydrocarbons of different structures.

E. V. Sagadeev; V. V. Sagadeev

2006-07-01T23:59:59.000Z

443

Calculation of the Heats of Combustion of Saturated Hydrocarbons Contained in Power-Generating Fuels  

Science Journals Connector (OSTI)

An empirical method is suggested for the calculation of the heats of combustion of saturated hydrocarbons by the additive scheme proceeding from their...

E. V. Sagadeev; V. V. Sagadeev

2002-07-01T23:59:59.000Z

444

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

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

with a DNA... ), a polycyclic aromatic hydrocarbon. A residue of fuel and tobacco combustion and frequently ingested by humans... , BP is metabolized in mammals to...

445

Low-Temperature Hydrocarbon/CO Oxidation Catalysis in Support of HCCI Emission Control  

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

Development of catalyst materials to facilitate the low-temperature oxidation of hydrocarbons and CO in homogeneous charge compression ignition (HCCI) emissions.

446

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

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

Blending Streams on "E85" Engine Optimization The Impact of Low Octane Hydrocarbon Blending Streams on "E85" Engine Optimization deer12szybist.pdf More Documents &...

447

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

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

hydrocarbon... to its high reactivity toward DNA and cellular proteins. The major acrolein-DNA adduct, -hydrox- ypropano... -hy- droxynonenal, and acrolein, that readily form...

448

E-Print Network 3.0 - aromatic hydrocarbon pah-degrading Sample...  

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

degradation Summary: Removal of polycyclic aromatic hydrocarbons (PAHs) from sewage sludge by anaerobic degradation N... , terminate in the sludge, and can be released to the...

449

Polycyclic Aromatic Hydrocarbons Formation in Sludge Incineration by Fluidised Bed and Rotary Kiln Furnace  

Science Journals Connector (OSTI)

Polycyclic Aromatic Hydrocarbons (PAHs) are typical pollutants arising from incineration. They are produced in any incomplete combustion principally due to inhomogeneities in a combustion chamber. The effects ...

Giuseppe Mininni; Andrea Sbrilli; Ettore Guerriero…

2004-05-01T23:59:59.000Z

450

Polycyclic aromatic hydrocarbon (PAH) in four fish species from different trophic levels in the Persian Gulf  

Science Journals Connector (OSTI)

Concentration of ten polycyclic aromatic hydrocarbon (PAH) compounds were determined in liver of four fish species from different trophic levels (Aurigequula fasciata, omnivore; Alepes djedaba, carnivore; Liza ab...

Shirin Rahmanpour; Nasrin Farzaneh Ghorghani…

2014-11-01T23:59:59.000Z

451

E-Print Network 3.0 - active aryl hydrocarbon Sample Search Results  

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

Receptors in Fishes Summary: the aryl hydrocarbon receptor (AHR), through which dioxins and dioxin-like compounds cause altered gene... -methylcholanthrene AHH: aryl...

452

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

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

bases in Iraq and Afghanistan that lack Summary: Compounds Toxic Organic Halogenated Dioxins Furans (dioxins) Polycyclic Aromatic Hydrocarbons found... and detected all of the...

453

E-Print Network 3.0 - aryl hydrocarbon receptor-dna Sample Search...  

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

Receptors in Fishes Summary: the aryl hydrocarbon receptor (AHR), through which dioxins and dioxin-like compounds cause altered gene... -methylcholanthrene AHH: aryl...

454

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

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

coal, oil, gas... called aromatic hydrocarbons. These include harmful pollutants like dioxins, PCBs and a group called Source: Rock, Chris - Department of Biological Sciences,...

455

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

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

S0045-6535(02)00145-5 Summary: Abstract Polycyclic aromatic hydrocarbons (PAHs) and dioxins are lipophilic organic pollutants occurring... absorption, pig INTRODUCTION...

456

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

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

Receptors in Fishes Summary: the aryl hydrocarbon receptor (AHR), through which dioxins and dioxin-like compounds cause altered gene... -methylcholanthrene AHH: aryl...

457

E-Print Network 3.0 - aryl hydrocarbon monooxygenase Sample Search...  

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

Receptors in Fishes Summary: the aryl hydrocarbon receptor (AHR), through which dioxins and dioxin-like compounds cause altered gene... -methylcholanthrene AHH: aryl...

458

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

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

S0045-6535(02)00145-5 Summary: Abstract Polycyclic aromatic hydrocarbons (PAHs) and dioxins are lipophilic organic pollutants occurring... absorption, pig INTRODUCTION...

459

E-Print Network 3.0 - aryl hydrocarbon receptor-regulated Sample...  

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

classes of the aryl hydrocarbon receptor (AHR). A grander objective is to provide... pollutants is a direct consequence of their interactions with the aryl ... Source: Bradfield,...

460

E-Print Network 3.0 - aryl hydrocarbon receptor-1 Sample Search...  

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

PARENTAL FACTORS ON GAMETE CONDITION AND VIABILITY Summary: . 15. 16. 17. 18-21. 22. Pollutants - petroleum aromatic hydrocarbons, aryl Pollutants - pesticides... high levels of...

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


461

E-Print Network 3.0 - aryl hydrocarbon nuclear Sample Search...  

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

Receptors in Fishes Summary: the aryl hydrocarbon receptor (AHR), through which dioxins and dioxin-like compounds cause altered gene... -methylcholanthrene AHH: aryl...

462

E-Print Network 3.0 - ahr aryl hydrocarbon Sample Search Results  

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

Receptors in Fishes Summary: the aryl hydrocarbon receptor (AHR), through which dioxins and dioxin-like compounds cause altered gene... -methylcholanthrene AHH: aryl...

463

E-Print Network 3.0 - aromatic hydrocarbon water-soluble Sample...  

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

S0045-6535(02)00145-5 Summary: Abstract Polycyclic aromatic hydrocarbons (PAHs) and dioxins are lipophilic organic pollutants occurring... with their lipophilicity and water...

464

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

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

WH, Caton JE. 1983. Extraction of polycyclic aromatic hydrocarbons for qualitative analysis. In... : Handbook of Polycyclic Aromatic ... Source: Rock, Chris - Department of...

465

E-Print Network 3.0 - aryl hydrocarbon receptor-independent Sample...  

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

PARENTAL FACTORS ON GAMETE CONDITION AND VIABILITY Summary: . 15. 16. 17. 18-21. 22. Pollutants - petroleum aromatic hydrocarbons, aryl Pollutants - pesticides... high levels of...

466

E-Print Network 3.0 - aryl hydrocarbon receptor-mediated Sample...  

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

4 TOXICOLOGICAL SCIENCES 106(1), 8392 (2008) doi:10.1093toxscikfn149 Summary: ). Analysis of aryl hydrocarbon receptor-mediated signaling during physiological hypoxia reveals...

467

E-Print Network 3.0 - aryl hydrocarbon receptor-dependent Sample...  

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

Receptors in Fishes Summary: the aryl hydrocarbon receptor (AHR), through which dioxins and dioxin-like compounds cause altered gene... -methylcholanthrene AHH: aryl...

468

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

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

Receptors in Fishes Summary: the aryl hydrocarbon receptor (AHR), through which dioxins and dioxin-like compounds cause altered gene... -methylcholanthrene AHH: aryl...

469

E-Print Network 3.0 - aromatic hydrocarbon-contaminated soil...  

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

soil... hydrocarbon degraders, and polycyclic aromatic ... Source: Ma, Lena - Soil and Water Science Department, University of Florida Collection: Environmental Sciences and...

470

Examination of polycyclic aromatic hydrocarbons in an urban stormwater system and bioaccumulation in Odonata.  

E-Print Network (OSTI)

??Polycyclic aromatic hydrocarbons (PAHs) are toxic organic pollutants produced from combustion processes. Associated with urban runoff they have been detected worldwide in urban wetlands. PAH… (more)

Heintzman, Lucas

2013-01-01T23:59:59.000Z

471

Problems in Catalytic Oxidation of Hydrocarbons and Detailed Simulation of Combustion Processes.  

E-Print Network (OSTI)

??This dissertation research consists of two parts, with Part I on the kinetics of catalytic oxidation of hydrocarbons and Part II on aspects on the… (more)

Xin, Yuxuan

2014-01-01T23:59:59.000Z

472

New IR Fiber-Optic Chemical Sensor for in Situ Measurements of Chlorinated Hydrocarbons in Water  

Science Journals Connector (OSTI)

In this work the development and validation of a new MIR fiber-optic physicochemical sensor system for the continuous in situ analysis of chlorinated hydrocarbons (CHCs) in...

Krska, R; Taga, K; Kellner, R

1993-01-01T23:59:59.000Z

473

Detection of Hydrocarbons in Water by MIR Evanescent-Wave Spectroscopy with Flattened Silver Halide Fibers  

Science Journals Connector (OSTI)

IR transmitting AgClxBr1-x fibers were used as internal reflection elements for the spectroscopic detection of hydrocarbons that are dissolved in water in an...

Hahn, P; Tacke, M; Jakusch, M; Mizaikoff, B; Spector, O; Katzir, A

2001-01-01T23:59:59.000Z

474

Characterization of hydrocarbons found in the arctic aquatic environment near the Ekati diamond mine.  

E-Print Network (OSTI)

??Polycyclic aromatic hydrocarbons (PAHs) in the aquatic environment of the Ekati Diamond Mine were evaluated in snow, sediment, air and water (via passive membrane samplers).… (more)

Nabess, Stephanie Ann

2014-01-01T23:59:59.000Z

475

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

SciTech Connect

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

476

The reactivity of cesium nickel ferrocyanide towards nitrate and nitrite salts  

SciTech Connect

Beginning in late 1988, the Pacific Northwest Laboratory (PNL) began an experimental program at the request of Westinghouse Hanford Company (WHC) to investigate the effects of temperature on the oxidation reaction between synthetic nickel cesium ferrocyanide (FeCN) and nitrates and nitrites representative of materials present in some of the Hanford single-shell tanks (SSTs). After completing a preliminary series of experiments in 1988, the program was expanded to include five tasks to evaluate the effect of selected compositional and operational parameters on the reaction and explosion temperatures of FeCN and nitrate and/or nitrite mixtures. 10 refs., 4 figs., 6 tabs.

Burger, L.L.; Scheele, R.D.

1991-09-01T23:59:59.000Z

477

Molecular biology of environmental aromatic hydrocarbons. Progress report, September 1, 1985-July 31, 1986  

SciTech Connect

Recent studies in our laboratory have indicated that short DNA oligonucleotides can be used as targets for alkylation by activated benzo(a)pyrene diol epoxide (BPDE) to examine the effect of PAH-induced mutagenesis. The alkylated oligomers are ligated into viral DNA and this construct is used to tranfect Escherichia coli. Progeny virus are selected from agar plates, amplified, and the viral DNA isolated is sequenced at the site of oligomer insertion. A scheme for the assembly of synthetic DNA oligonucleotides has been devised such that: (a) the site of alkylation in the oligomer is specific for a single deoxynucleotide species; and (b) the position of the adduct(s) in the oligomer can be varied. At the present stage of our work, we have prepared four synthetic duplex DNA oligomers. These oligomers are 32 base pairs in length and contain either a single or double dG residue in each strand separated by 4 or 12 base pairs (see text in this report). When these oligomers are reacted with (+)BPDE, only the dG residues form adducts. Transfection of E. coli with the four different assembled oligomers alkylated with (+)BPDE gives rise to the production of progency viral DNAs which primarily show the restoration of the original ologomer DNA sequence, but also, the appearance of a large deletion at the site of alkylation. The number of progeny viral DNAs sequenced to date are too few to determine a reliable mutation frequency. Construction of DNA oligomers containing other alkylated residues, e.g., dA and dC, is in progress. Preliminary attempts to detect BPDE-induced enzymes that participate in the repair of PAH-damaged DNA are also described. 27 refs., 1 fig.

Weiss, S.B.

1986-08-01T23:59:59.000Z

478

NITRATE UTILIZATION BY PHYTOPLANKTON IN LAKE SUPERIOR IS IMPAIRED BY LOW NUTRIENT (P, Fe) AVAILABILITY AND SEASONAL LIGHT LIMITATION--  

E-Print Network (OSTI)

NITRATE UTILIZATION BY PHYTOPLANKTON IN LAKE SUPERIOR IS IMPAIRED BY LOW NUTRIENT (P, Fe utilization in this oligotrophic system. Clean sampling methods were used to collect water from Lake Superior during spring and summer 2004, and nitrate utilization was measured by monitoring bioreporter

Sterner, Robert W.

479

Change in Bacterial Community Structure during In Situ Biostimulation of Subsurface Sediment Cocontaminated with Uranium and Nitrate  

Science Journals Connector (OSTI)

...403-410. 2 American Public Health Association. 1969...604-609. American Public Health Association, Washington...Geobacter species to remove uranium from the groundwater...nitrate, Fe(III), and uranium were extensively reduced...while nitrate was largely depleted. A large diversity of...

Nadia N. North; Sherry L. Dollhopf; Lainie Petrie; Jonathan D. Istok; David L. Balkwill; Joel E. Kostka

2004-08-01T23:59:59.000Z

480

Structural Changes of Bimetallic PdX/Cu (1-X) Nanocatalysts Developed for Nitrate Reduction of Drinking Water  

E-Print Network (OSTI)

of Drinking Water Huiping Xu1,2 , Ray Twesten3 , Kathryn Guy4 , John Shapley4 , Charles Werth5 , Anatoly alternative for nitrate removal in drinking water [1]. Fundamental understanding how the atomic arrangement for the purification of drinking water. INTRODUCTION Presently nitrate in drinking water is either not removed

Frenkel, Anatoly

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481

Catalysts and process for liquid hydrocarbon fuel production  

DOE Patents (OSTI)

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

White, Mark G; Liu, Shetian

2014-12-09T23:59:59.000Z

482

Application of a modified denitrifying bacteria method for analyzing groundwater and vadose zone pore water nitrate at the Hanford Site, WA, USA.  

E-Print Network (OSTI)

zone pore water nitrate at the Hanford Site, WA, USA. Woods,and Conrad, Mark The Hanford Site in southern WashingtonL have been reported for Hanford groundwaters, where nitrate

Woods, Katharine N.; Singleton, Michael J.; Conrad, Mark

2003-01-01T23:59:59.000Z

483

California GAMA Special Study: An isotopic and dissolved gas investigation of nitrate source and transport to a public supply well in California's Central Valley  

SciTech Connect

This study investigates nitrate contamination of a deep municipal drinking water production well in Ripon, CA to demonstrate the utility of natural groundwater tracers in constraining the sources and transport of nitrate to deep aquifers in the Central Valley. The goal of the study was to investigate the origin (source) of elevated nitrate and the potential for the deep aquifer to attenuate anthropogenic nitrate. The site is ideal for such an investigation. The production well is screened from 165-325 feet below ground surface and a number of nearby shallow and deep monitoring wells were available for sampling. Furthermore, potential sources of nitrate contamination to the well had been identified, including a fertilizer supply plant located approximately 1000 feet to the east and local almond groves. A variety of natural isotopic and dissolved gas tracers including {sup 3}H-{sup 3}He groundwater age and the isotopic composition of nitrate are applied to identify nitrate sources and to characterize nitrate transport. An advanced method for sampling production wells is employed to help identify contaminant contributions from specific screen intervals. Nitrate transport: Groundwater nitrate at this field site is not being actively denitrified. Groundwater parameters indicate oxic conditions, the dissolved gas data shows no evidence for excess nitrogen as the result of denitrification, and nitrate-N and -O isotope compositions do not display patterns typical of denitrification. Contaminant nitrate source: The ambient nitrate concentration in shallow groundwater at the Ripon site ({approx}12 mg/L as nitrate) is typical of shallow groundwaters affected by recharge from agricultural and urban areas. Nitrate concentrations in Ripon City Well 12 (50-58 mg/L as nitrate) are significantly higher than these ambient concentrations, indicating an additional source of anthropogenic nitrate is affecting groundwater in the capture zone of this municipal drinking water well. This study provides two new pieces of evidence that the Ripon Farm Services Plant is the source of elevated nitrate in Ripon City Well 12. (1) Chemical mass balance calculations using nitrate concentration, nitrate isotopic composition, and initial tritium activity all indicate that that the source water for elevated nitrate to Ripon City Well 12 is a very small component of the water produced by City Well 12 and thus must have extremely high nitrate concentration. The high source water nitrate concentration ({approx}1500 mg/L as nitrate) required by these mass balance calculations precludes common sources of nitrate such as irrigated agriculture, dairy wastewater, and septic discharge. Shallow groundwater under the Ripon Farm Services RFS plant does contain extremely high concentrations of nitrate (>1700 mg/L as nitrate). (2) Nitrogen and oxygen isotope compositions of nitrate indicate that the additional anthropogenic nitrate source to Ripon City Well 12 is significantly enriched in {delta}{sup 18}O-NO{sub 3}, an isotopic signature consistent with synthetic nitrate fertilizer, and not with human or animal wastewater discharge (i.e. dairy operations, septic system discharge, or municipal wastewater discharge), or with organic fertilizer. Monitoring wells on and near the RFS plant also have high {delta}{sup 18}O-NO{sub 3}, and the plant has handled and stored synthetic nitrate fertilizer that will have this isotopic signature. The results described here highlight the complexity of attributing nitrate found in long screened, high capacity wells to specific sources. In this case, the presence of a very high concentration source near the well site combined with sampling using multiple isotopic tracer techniques and specialized depth-specific techniques allowed fingerprinting of the source in the mixed-age samples drawn from the production well.

Singleton, M J; Moran, J E; Esser, B K; Roberts, S K; Hillegonds, D J

2010-04-14T23:59:59.000Z

484

Inhibition of Protein Tyrosine Phosphatase by the Antitumor Agent Gallium Nitrate  

Science Journals Connector (OSTI)

...Gallium is known to bind to the iron transport protein transferrin...NSC 166828. gallium, tris(acetylacetonate). The gallium nitrate:transferrin...the binding of gallium to the iron transport protein transferrin...and incorporation into the iron storage protein ferritin...

Margareta M. Berggren; Leigh Ann Burns; Robert T. Abraham; and Garth Powis

1993-04-15T23:59:59.000Z

485

Nitrate and colloid transport through coarse Hanford sediments under steady state, variably saturated flow  

E-Print Network (OSTI)

Nitrate and colloid transport through coarse Hanford sediments under steady state, variably] At the U.S. Department of Energy's Hanford Reservation, colloid-facilitated transport is a potential of colloids through Hanford sediments under steady state, unsaturated flow conditions. We isolated colloids

Flury, Markus

486

Applicability of Anaerobic Nitrate-Dependent Fe(II) Oxidation to Microbial Enhanced Oil Recovery (MEOR)  

Science Journals Connector (OSTI)

Furthermore, both of the substrates of the NDFO organisms [Fe(II) and nitrate] and the various end products of the metabolism [Fe(III), nitrite, nitric oxide, and nitrous oxide] all have known anti-souring and sulfide-scouring activities. ... A glass wool pad was placed on the bottom of the bead beds to prevent beads from falling into the inlet tubing. ...

Hongbo Zhu; Han K. Carlson; John D. Coates

2013-06-25T23:59:59.000Z

487

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

E-Print Network (OSTI)

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

Benning, Liane G.

488

Quantifying uncertainty in nitrate pollution from land application of sewage sludge  

SciTech Connect

Uncertainty associated with nitrate-nitrogen pollution of ground water from sludge applications was investigated. Three alternative planning models were proposed. The models estimate annual loads and concentrations of nitrate-nitrogen in percolation. Published data from four field studies that included aerobic and anaerobic sludge and surface- and soil-incorporated applications were used for model testing. Point and stochastic validation procedures were used. The models were generally conservative. For three data sets average relative errors were approximately +/- 25% for all three models. The fourth data set had average relative errors of 100-500%. Wilcoxon Signed Rank test results (at ..cap alpha.. = 5%) suggested point-model predictions and observations were drawn from similar distributions. Stochastic validation tests also suggested that observations were samples from distributions of predictions. The models were tested as uncalibrated approximations of nitrate percolation. All three appear sufficiently accurate for planning application systems. A planning procedure was developed which utilizes analytically approximated probability distributions of nitrate loads and concentrations. Distributions are specified with analytical moment expressions and a normal distribution function limited to be non-negative.

Mummert, M.C.

1987-01-01T23:59:59.000Z

489

Carbon 14 Production From Ammonium Nitrate Solution in the Chain-reacting Pile  

Science Journals Connector (OSTI)

...expected, there is also dissolved in the solution a small residual amount of C1402 which can be recovered easily by 0M14 AC PILC FIG. 1. C14 factory using circulating solution of ammonium nitrate. that most of the C14 would be evolved from such a solution...

L. D. NORRIS; ARTHUR H. SNELL

1947-03-07T23:59:59.000Z

490

High-Resolution In Situ Analysis of Nitrate and Phosphate in the Oligotrophic Ocean  

Science Journals Connector (OSTI)

High-Resolution In Situ Analysis of Nitrate and Phosphate in the Oligotrophic Ocean ... Upon power up, the instrument will sequentially execute all commands in the current method until termination by lack of further commands or power interruption. ... The SEAS instrument was connected to a CTD and a PAR sensor, powered on deck, and lowered to 30 m depth. ...

Lori R. Adornato; Eric A. Kaltenbacher; Danielle R. Greenhow; Robert H. Byrne

2007-05-04T23:59:59.000Z

491

Acetate Production from Oil under Sulfate-Reducing Conditions in Bioreactors Injected with Sulfate and Nitrate  

Science Journals Connector (OSTI)

...sulfate- and nitrate- reducing bacteria from an oil field in Argentina. Appl. Environ. Microbiol. 74 :4324-4335. 34. Callbeck...6908-6917. 41. Gieg, LM , KE Duncan and JM Suflita. 2008. Bioenergy production via microbial conversion of residual oil to natural...

Cameron M. Callbeck; Akhil Agrawal; Gerrit Voordouw

2013-06-14T23:59:59.000Z

492

The structure of the complex formed by tetrahethylamalondiamide and lanthanum(III) nitrate  

Science Journals Connector (OSTI)

The structure of the complex LaL2(NO3)3 [L = (C2H5)2NCOCH2CON(C2H5)2] has been investigated. It has been shown that the lanthanum is 10 coordinate with two bidentate L ligands and three bidentate nitrate groups.

Paul Byers; Michael G.B. Drew; Michael J. Hudson; Neil S. Isaacs; Charles Madic

1994-01-01T23:59:59.000Z

493

Application of a modified denitrifying bacteria method for analyzing groundwater and vadose zone pore water nitrate at the Hanford Site, WA, USA.  

E-Print Network (OSTI)

the Hanford Site, WA, USA. Woods, Katharine N. ; Singleton,reside at DOE sites across the USA. Nitrate concentrations >

Woods, Katharine N.; Singleton, Michael J.; Conrad, Mark

2003-01-01T23:59:59.000Z

494

Mach 2 combustion characteristics of hydrogen/hydrocarbon fuel mixtures  

SciTech Connect

The combustion of H/sub 2//CH/sub 4/ and H/sub 2//C/sub 2/H/sub 4/ mixtures containing 10 to 70 vol pct hydrocarbon at combustor inlet Mach number 2 and temperatures 2000 to 4000 R is investigated experimentally, applying direct-connect test hardware and techniques similar to those described by Diskin and Northam (1987) in the facilities of the NASA Langley Hypersonic Propulsion Branch. The experimental setup, procedures, and data-reduction methods are described; and the results are presented in extensive tables and graphs and characterized in detail. Fuel type and mixture are found to have little effect on the wall heating rate measured near the combustor exit, but H/sub 2//C/sub 2/H/sub 4/ is shown to burn much more efficiently than H/sub 2//CH/sub 4/, with no pilot-off blowout equivalence ratios greater than 0.5. It is suggested that H/sub 2//hydrocarbon mixtures are feasible fuels (at least in terms of combustion efficiency) for scramjet SSTO vehicles operating at freestream Mach numbers above 4.

Diskin, G.S.; Jachimowski, C.J.; Northam, G.B.; Bell, R.A.

1987-01-01T23:59:59.000Z

495

Oxygen sensor for monitoring gas mixtures containing hydrocarbons  

DOE Patents (OSTI)

A gas sensor measures O.sub.2 content of a reformable monitored gas containing hydrocarbons H.sub.2 O and/or CO.sub.2, preferably in association with an electrochemical power generation system. The gas sensor has a housing communicating with the monitored gas environment and carries the monitored gas through an integral catalytic hydrocarbon reforming chamber containing a reforming catalyst, and over a solid electrolyte electrochemical cell used for sensing purposes. The electrochemical cell includes a solid electrolyte between a sensor electrode that is exposed to the monitored gas, and a reference electrode that is isolated in the housing from the monitored gas and is exposed to a reference gas environment. A heating element is also provided in heat transfer communication with the gas sensor. A circuit that can include controls operable to adjust operations via valves or the like is connected between the sensor electrode and the reference electrode to process the electrical signal developed by the electrochemical cell. The electrical signal varies as a measure of the equilibrium oxygen partial pressure of the monitored gas. Signal noise is effectively reduced by maintaining a constant temperature in the area of the electrochemical cell and providing a monitored gas at chemical equilibria when contacting the electrochemical cell. The output gas from the electrochemical cell of the sensor is fed back into the conduits of the power generating system.

Ruka, Roswell J. (Pittsburgh, PA); Basel, Richard A. (Pittsburgh, PA)

1996-01-01T23:59:59.000Z

496

Preliminary Economics for Hydrocarbon Fuel Production from Cellulosic Sugars  

SciTech Connect

Biorefinery process and economic models built in CHEMCAD and a preliminary, genome-scale metabolic model for the oleaginous yeast Lipomyces starkeyi were used to simulate the bioconversion of corn stover to lipids, and the upgrading of these hydrocarbon precursors to diesel and jet fuel. The metabolic model was based on the recently released genome sequence for L. starkeyi and on metabolic pathway information from the literature. The process model was based on bioconversion, lipid extraction, and lipid oil upgrading data found in literature, on new laboratory experimental data, and on yield predictions from the preliminary L. starkeyi metabolic model. The current plant gate production cost for a distillate-range hydrocarbon fuel was estimated by the process model Base Case to be $9.5/gallon ($9.0 /gallon of gasoline equivalent) with assumptions of 2011$, 10% internal return on investment, and 2205 ton/day dry feed rate. Opportunities for reducing the cost to below $5.0/gallon, such as improving bioconversion lipid yield and hydrogenation catalyst selectivity, are presented in a Target Case. The process and economic models developed for this work will be updated in 2014 with new experimental data and predictions from a refined metabolic network model for L. starkeyi. Attaining a production cost of $3.0/gallon will require finding higher value uses for lignin other than power generation, such as conversion to additional fuel or to a co-product.

Collett, James R.; Meyer, Pimphan A.; Jones, Susanne B.

2014-05-18T23:59:59.000Z

497

Oxygen sensor for monitoring gas mixtures containing hydrocarbons  

DOE Patents (OSTI)

A gas sensor measures O{sub 2} content of a reformable monitored gas containing hydrocarbons, H{sub 2}O and/or CO{sub 2}, preferably in association with an electrochemical power generation system. The gas sensor has a housing communicating with the monitored gas environment and carries the monitored gas through an integral catalytic hydrocarbon reforming chamber containing a reforming catalyst, and over a solid electrolyte electrochemical cell used for sensing purposes. The electrochemical cell includes a solid electrolyte between a sensor electrode that is exposed to the monitored gas, and a reference electrode that is isolated in the housing from the monitored gas and is exposed to a reference gas environment. A heating element is also provided in heat transfer communication with the gas sensor. A circuit that can include controls operable to adjust operations via valves or the like is connected between the sensor electrode and the reference electrode to process the electrical signal developed by the electrochemical cell. The electrical signal varies as a measure of the equilibrium oxygen partial pressure of the monitored gas. Signal noise is effectively reduced by maintaining a constant temperature in the area of the electrochemical cell and providing a monitored gas at chemical equilibria when contacting the electrochemical cell. The output gas from the electrochemical cell of the sensor is fed back into the conduits of the power generating system. 4 figs.

Ruka, R.J.; Basel, R.A.

1996-03-12T23:59:59.000Z

498

Distillation sequence for the purification and recovery of hydrocarbons  

DOE Patents (OSTI)

This invention is an improved distillation sequence for the separation and purification of ethylene from a cracked gas. A hydrocarbon feed enters a C2 distributor column. The top of the C2 distributor column is thermally coupled to an ethylene distributor column, and the bottoms liquid of a C2 distributor column feeds a deethanizer column. The C2 distributor column utilizes a conventional reboiler. The top of the ethylene distributor is thermally coupled with a demethanizer column, and the bottoms liquid of the ethylene distributor feeds a C2 splitter column. The ethylene distributor column utilizes a conventional reboiler. The deethanizer and C2 splitter columns are also thermally coupled and operated at a substantially lower pressure than the C2 distributor column, the ethylene distributor column, and the demethanizer column. Alternatively, a hydrocarbon feed enters a deethanizer column. The top of the deethanizer is thermally coupled to an ethylene distributor column, and the ethylene distributor column utilizes a conventional reboiler. The top of the ethylene distributor column is thermally coupled with a demethanizer column, and the bottoms liquid of the ethylene distributor column feeds a C2 splitter column. The C2 splitter column operates at a pressure substantially lower than the ethylene distributor column, the demethanizer column, and the deethanizer column.

Reyneke, Rian (Katy, TX); Foral, Michael (Aurora, IL); Papadopoulos, Christos G. (Naperville, IL); Logsdon, Jeffrey S. (Naperville, IL); Eng, Wayne W. Y. (League City, TX); Lee, Guang-Chung (Houston, TX); Sinclair, Ian (Warrington, GB)

2007-12-25T23:59:59.000Z

499

Mutual solubilities of water and hydrocarbons from the Cubic plus Association equation of state: A new mixing rule for the correlation of observed minimum hydrocarbon solubilities  

Science Journals Connector (OSTI)

Abstract The cubic plus association (CPA) equation of state was employed to correlate the mutual solubilities of water and hydrocarbons (n-alkanes, cycloalkanes and aromatics). In order to reproduce the minimums observed in concentration vs. temperature curves, a new mixing rule is proposed based on Kabadi and Danner's idea, whereby the water–water dispersive term is corrected to include the hydrophobic hydration effect. With this correction, correlated hydrocarbon solubilities curves have observable curvature at low temperatures. Two binary interaction parameters are required for saturated hydrocarbons and three for aromatics, which is just one more than the original CPA formulation. Using parameters determined from binary data, this improved mixing rule was employed for multicomponent water–hydrocarbon systems, with no further regression, producing better predictions when compared to the conventional van der Waals’ rules.

Milton Medeiros

2014-01-01T23:59:59.000Z

500

Desiccant bed on hydrocarbon charged to and removed from underground (salt) cavern  

SciTech Connect

A hydrocarbon fluid storage system is described which consists of in operable conjunction: a cavern formed within an underground salt strata below a ground surface, the cavern comprises a lower liquid volume of saturated sodium chloride storage brine and an upper fluid volume of wet hydrocarbon storage fluid, surface fluid handling means; conduit connecting the lower storage brine and upper storage hydrocarbon fluid with the surface fluid handling means, of fluid transfer means enabling transfer of brine and hydrocarbon fluid from the surface to the cavern and from the cavern to the surface, such that brine can be added to or withdrawn from the lower brine volume and hydrocarbon fluids can be added to or withdrawn from the upper hydrocarbon fluid volume, and at least one desiccant drier means positioned at the surface in operable association with the surface fluid handling means whereby the wet hydrocarbon fluid upon withdrawal from the cavern passes through the desiccant drier means and thereby becomes dry, and dry hydrocarbon fluid intended for storage passes through the desiccant drier prior to entering the storage cavern and thereby becomes wet.

Washer, S.P.

1986-06-03T23:59:59.000Z