Science.gov

Sample records for mesozoic-paleozoic hydrocarbon resource-rocks

  1. Hydrocarbon pneumonia

    MedlinePlus

    Pneumonia - hydrocarbon ... Coughing Fever Shortness of breath Smell of a hydrocarbon product on the breath Stupor (decreased level of ... Most children who drink or inhale hydrocarbon products and develop ... hydrocarbons may lead to rapid respiratory failure and death.

  2. Apparatus for hydrocarbon extraction

    DOEpatents

    Bohnert, George W.; Verhulst, Galen G.

    2013-03-19

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

  3. Combustion of viscous hydrocarbons

    SciTech Connect

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

    1987-08-04

    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.

  4. Recovering hydrocarbons from hydrocarbon-containing vapors

    DOEpatents

    Mirza, Zia I.; Knell, Everett W.; Winter, Bruce L.

    1980-09-30

    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.

  5. Oxygenated Derivatives of Hydrocarbons

    Technology Transfer Automated Retrieval System (TEKTRAN)

    For the book entitled “Insect Hydrocarbons: Biology, Biochemistry and Chemical Ecology”, this chapter presents a comprehensive review of the occurrence, structure and function of oxygenated derivatives of hydrocarbons. The book chapter focuses on the occurrence, structural identification and functi...

  6. Hydrocarbon Spectral Database

    National Institute of Standards and Technology Data Gateway

    SRD 115 Hydrocarbon Spectral Database (Web, free access)   All of the rotational spectral lines observed and reported in the open literature for 91 hydrocarbon molecules have been tabulated. The isotopic molecular species, assigned quantum numbers, observed frequency, estimated measurement uncertainty and reference are given for each transition reported.

  7. Plasma Processing Of Hydrocarbon

    SciTech Connect

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

    2007-05-01

    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.

  8. Hydrocarbon treating process

    SciTech Connect

    Verachtert, T. A.

    1984-11-06

    A process is disclosed for treating hydrocarbon streams such as naphtha by the oxidation of mercaptans into disulfide compounds which remain in the hydrocarbon stream. The conversion is effected during passage of the hydrocarbon and an aqueous stream downward through a cylindrical mass of liquid-liquid contact material. The liquids then flow through a cylindrical screen into an annular separation zone which surrounds a lower part of the contact material. After decantation in the separation zone, the aqueous material, which preferably contains the oxidation catalyst, is recycled.

  9. Hydrocarbon recovery from diatomite

    SciTech Connect

    Scinta, J.

    1984-05-15

    Supercritical extraction of diatomaceous earth results in a much more significant improvement in hydrocarbon recovery over Fischer retorting than achievable with tar sands. Process and apparatus for supercritical extraction of diatomaceous earth are disclosed.

  10. Membrane separation of hydrocarbons

    DOEpatents

    Funk, Edward W.; Kulkarni, Sudhir S.; Chang, Y. Alice

    1986-01-01

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

  11. Hydrocarbon geoscience research strategy

    SciTech Connect

    Not Available

    1990-04-01

    This document outlines a strategy for oil and gas related research focused on optimizing the economic producibility of the Nation's resources. The Hydrocarbon Geoscience Strategy was developed by the Hydrocarbon Geoscience Research Coordinating Committee of the Department of Energy (DOE). This strategy forms the basis for the development of DOE Fossil Energy's Oil Research Program Implementation Plan and Natural Gas Program Implementation Plan. 24 refs., 5 figs., 3 tabs.

  12. Thermal cracking of hydrocarbons

    SciTech Connect

    Braun, R.L.; Burnham, A.K.

    1988-09-01

    Knowledge of thermal cracking of hydrocarbons is important in understanding and modeling petroleum maturation. We have reviewed the literature on the thermal cracking of pure hydrocarbons and mixtures of hydrocarbons, with particular attention given to dependence of the kinetics on temperature, pressure, and phase. Major uncertainties remain with regard to pressure dependence. Based on this review, we developed a simple, four-component, three-reaction model for oil-cracking. We also developed a simple, kerogen-maturation, kinetic model that incorporates hydrogen and carbon balance and includes the most important oil- and gas-forming reactions: kerogen pyrolysis, three oil-cracking reactions, and three coke-pyrolysis reactions. Tentative stoichiometry parameters are given for lacustrine and marine kerogens. 35 refs., 5 figs., 5 tabs.

  13. Quantitative Hydrocarbon Surface Analysis

    NASA Technical Reports Server (NTRS)

    Douglas, Vonnie M.

    2000-01-01

    The elimination of ozone depleting substances, such as carbon tetrachloride, has resulted in the use of new analytical techniques for cleanliness verification and contamination sampling. The last remaining application at Rocketdyne which required a replacement technique was the quantitative analysis of hydrocarbons by infrared spectrometry. This application, which previously utilized carbon tetrachloride, was successfully modified using the SOC-400, a compact portable FTIR manufactured by Surface Optics Corporation. This instrument can quantitatively measure and identify hydrocarbons from solvent flush of hardware as well as directly analyze the surface of metallic components without the use of ozone depleting chemicals. Several sampling accessories are utilized to perform analysis for various applications.

  14. Hydrocarbon fuel detergent

    SciTech Connect

    Meyer, G.R.; Lyons, W.R.

    1990-01-23

    This patent describes a hydrocarbon fuel composition comprising: a hydrocarbon fuel; and a detergent amount of a detergent comprising an alkenylsuccinimide prepared by reacting an alkenylsuccinic acid or anhydride with a mixture of amines, wherein at least 90 weight percent of the alkenyl substituent is derived from an olefin having a carbon chain of from 10 to 30 carbons or mixtures thereof, and wherein the alkenylsuccinic acid or anhydride is reacted with the mixture of amines at a mole ratio of 0.8 to 1.5 moles of the amines per mole of the alkenylsuccinic acid or anhydride.

  15. HYDROCARBON POLLUTANTS FROM STATIONARY SOURCES

    EPA Science Inventory

    The report gives results of a study of hydrocarbon pollutants from stationary sources. Early in the study, readily available information was assembled on stationary sources of hydrocarbon emissions and effluents. Information was also obtained on process descriptions, operating pa...

  16. Selecting hydrocarbon rocket propulsion technology

    NASA Technical Reports Server (NTRS)

    Martin, J. A.

    1986-01-01

    Past studies have shown that the dry weight of future earth-to-orbit vehicles can be reduced by the combined use of hydrogen and hydrocarbon propulsion compared to all-hydrogen propulsion. This paper shows that the use of certain hydrocarbon engines with hydrogen engines produces the lowest vehicle dry mass. These hydrocarbon engines use propane or RP-1 fuel, hydrogen cooling, and hydrogen-rich gas generators. Integration of the hydrogen and hydrocarbon nozzles is also beneficial.

  17. Zeroing in on hydrocarbons

    SciTech Connect

    Roest, I.P.B. van der; Brasser, D.J.S.; Wagebaert, A.P.J.; Stam, P.H.

    1997-05-01

    The increasing costs of remediating contaminated sites has stimulated research for cost-reducing techniques in soil investigation and cleanup techniques. MAP Environmental Research has developed a technology using ground penetrating radar in combination with in house developed software to locate and define the extent of hydrocarbon contamination. This article discusses the new technology. 2 figs.

  18. Hydrocarbon options emerge

    SciTech Connect

    Fairley, P.

    1995-11-01

    Europe stole the scene at last week`s International Chlorofluorocarbon (CFC) and Halon Alternatives Conference in Washington as attendees learned more about an accelerating shift to low-cost hydrocarbon refrigerants by European equipment manufacturers. Udo Wenning, representing German refrigerator market leader Bosch-Siemens, told the conference that hydrocarbons-isobutane as refrigerant and cyclopentane to blow the insulating foam-are now used in 90% of German production. Wenning says that in all performance parameters, hydrocarbons match the hydrochlorofluorocarbon (HCFC) and hydrofluorocarbon (HFC) replacements favored in the U.S. and Japan and that, unlike HCFCs and HFCs they have low global warming potential. Their Achille`s heel is flammability, Wenning says. American equipment manufacturers aiming to sell a new generation of equipment designed for the new HFC refrigerants sought to amplify concern over flammability at the conference. {open_quotes}In a society as litigious as ours, we do not see a future for flammable refrigerants,{close_quotes} says a representative of air conditioner manufacturer Carrier. Hydrocarbon supporters such as Greenpeace say the risks are mananageable.

  19. Optrode for sensing hydrocarbons

    DOEpatents

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

    1987-05-19

    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.

  20. Optrode for sensing hydrocarbons

    DOEpatents

    Miller, Holly; Milanovich, Fred P.; Hirschfeld, Tomas B.; Miller, Fred S.

    1988-01-01

    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.

  1. Optrode for sensing hydrocarbons

    DOEpatents

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

    1988-09-13

    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.

  2. Optrode for sensing hydrocarbons

    DOEpatents

    Miller, Holly; Milanovich, Fred P.; Hirschfeld, Tomas B.; Miller, Fred S.

    1987-01-01

    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.

  3. Apparatus and methods for hydrocarbon extraction

    DOEpatents

    Bohnert, George W.; Verhulst, Galen G.

    2016-04-26

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

  4. Mantle hydrocarbons: Abiotic or biotic?

    SciTech Connect

    Sugisaki, Ryuichi; Mimura, Koichi

    1994-06-01

    Analyses of 227 rocks from fifty localities throughout the world showed that mantle derived rocks such as tectonized peridotites in ophiolite sequences (tectonites) and peridotite xenoliths in alkali basalts contain heavier hydrocarbons (n-alkanes), whereas igneous rocks produced by magmas such as gabbro and granite lack them. The occurrence of hydrocarbons indicates that they were not derived either from laboratory contamination or from field contamination; these compounds found in the mantle-derived rocks are called here {open_quotes}mantle hydrocarbons.{close_quotes} The existence of hydrocarbons correlates with petrogenesis. For example, peridotite cumulates produced by magmatic differentiation lack hydrocarbons whereas peridotite xenoliths derived from the mantle contain them. Gas chromatographic-mass spectrometric records of the mantle hydrocarbons resemble those of aliphatics in meteorites and in petroleum. Features of the hydrocarbons are that (a) the mantle hydrocarbons reside mainly along grain boundaries and in fluid inclusions of minerals; (b) heavier isoprenoids such as pristane and phytane are present; and (c) {delta}{sup 13}C of the mantle hydrocarbons is uniform (about {minus}27{per_thousand}). Possible origins for the mantle hydrocarbons are as follows. (1) They were inorganically synthesized by Fischer-Tropsch type reaction in the mantle. (2) They were delivered by meteorites and comets to the early Earth. (3) They were recycled by subduction. The mantle hydrocarbons in the cases of (1) and (2) are abiogenic and those in (3) are mainly biogenic. It appears that hydrocarbons may survive high pressures and temperatures in the mantle, but they are decomposed into lighter hydrocarbon gases such as CH{sub 4} at lower pressures when magmas intrude into the crust; consequently, peridotite cumulates do not contain heavier hydrocarbons but possess hydrocarbon gases up to C{sub 4}H{sub 10}. 76 refs., 5 figs., 3 tabs.

  5. Mantle hydrocarbons: abiotic or biotic?

    PubMed

    Sugisaki, R; Mimura, K

    1994-06-01

    Analyses of 227 rocks from fifty localities throughout the world showed that mantle derived rocks such as tectonized peridotites in ophiolite sequences (tectonites) arid peridotite xenoliths in alkali basalts contain heavier hydrocarbons (n-alkanes), whereas igneous rocks produced by magmas such as gabbro arid granite lack them. The occurrence of hydrocarbons indicates that they were not derived either from laboratory contamination or from held contamination; these compounds found in the mantle-derived rocks are called here "mantle hydrocarbons." The existence of hydrocarbons correlates with petrogenesis. For example, peridotite cumulates produced by magmatic differentiation lack hydrocarbons whereas peridotite xenoliths derived from the mantle contain them. Gas chromatographic-mass spectrometric records of the mantle hydrocarbons resemble those of aliphatics in meteorites and in petroleum. Features of the hydrocarbons are that (a) the mantle hydrocarbons reside mainly along grain boundaries and in fluid inclusions of minerals; (b) heavier isoprenoids such as pristane and phytane are present; and (c) delta 13C of the mantle hydrocarbons is uniform (about -27%). Possible origins for the mantle hydrocarbons are as follows. (1) They were in organically synthesized by Fischer-Tropsch type reaction in the mantle. (2) They were delivered by meteorites and comets to the early Earth. (3) They were recycled by subduction. The mantle hydrocarbons in the cases of (1) and (2) are abiogenic and those in (3) are mainly biogenic. It appears that hydrocarbons may survive high pressures and temperatures in the mantle, but they are decomposed into lighter hydrocarbon gases such as CH4 at lower pressures when magmas intrude into the crust; consequently, peridotite cumulates do not contain heavier hydrocarbons but possess hydrocarbon gases up to C4H10. PMID:11541663

  6. Mantle hydrocarbons: Abiotic or biotic?

    NASA Astrophysics Data System (ADS)

    Sugisaki, Ryuichi; Mimura, Koichi

    1994-06-01

    Analyses of 227 rocks from fifty localities throughout the world showed that mantle derived rocks such as tectonized peridotites in ophiolite sequences (tectonites) and peridotite xenoliths in alkali basalts contain heavier hydrocarbons ( n-alkanes), whereas igneous rocks produced by magmas such as gabbro and granite lack them. The occurrence of hydrocarbons indicates that they were not derived either from laboratory contamination or from field contamination; these compounds found in the mantle-derived rocks are called here "mantle hydrocarbons." The existence of hydrocarbons correlates with petrogenesis. For example, peridotite cumulates produced by magmatic differentiation lack hydrocarbons whereas peridotite xenoliths derived from the mantle contain them. Gas Chromatographic—mass spectrometric records of the mantle hydrocarbons resemble those of aliphatics in meteorites and in petroleum. Features of the hydrocarbons are that (a) the mantle hydrocarbons reside mainly along grain boundaries and in fluid inclusions of minerals (b) heavier isoprenoids such as pristane and phytane are present (c) δ13C of the mantle hydrocarbons is uniform (about -27%.). Possible origins for the mantle hydrocarbons are as follows. (1) They were inorganically synthesized by Fischer-Tropsch type reaction in the mantle. (2) They were delivered by meteorites and comets to the early Earth. (3) They were recycled by subduction. The mantle hydrocarbons in the cases of (1) and (2) are abiogenic and those in (3) are mainly biogenic. It appears that hydrocarbons may survive high pressures and temperatures in the mantle, but they are decomposed into lighter hydrocarbon gases such as CH 4 at lower pressures when magmas intrude into the crust; consequently, peridotite cumulates do not contain heavier hydrocarbons but possess hydrocarbon gases up to C 4H 10.

  7. Bacterial sources for phenylalkane hydrocarbons

    SciTech Connect

    Ellis, L.; Winans, R.E.; Langworthy, T.

    1996-10-01

    The presence of phenylalkane hydrocarbons in geochemical samples has been the source of much controversy. Although an anthropogenic input from detergent sources always appears likely, the distribution of phenylalkane hydrocarbons in some cases far exceeding that attributed to detergent input has led to a reappraisal of this view. Indeed, recent work involving analysis of the lipid hydrocarbon extracts from extant Thermoplasma bacteria has revealed the presence of phenylalkane hydrocarbons. The presence of phenylalkane hydrocarbons in sedimentary organic matter may therefore represent potential biological markers for thermophilic bacteria.

  8. Sulfur removal from hydrocarbons

    SciTech Connect

    Pearce, R.L.; Wolcott, R.A.

    1989-02-28

    A method is described for treating liquid and gaseous hydrocarbon streams containing H/sub 2/S, CO/sub 2/ and COS to remove a substantial portion of the H/sub 2/S and COS, and slip a substantial portion of the CO/sub 2/ which comprises: contacting the hydrocarbon stream containing H/sub 2/S, CO/sub 2/ and COS with a solution of methyldiethanolamine, which is a selective absorbent for H/sub 2/S with respect to CO/sub 2/, and which solution also contains diisopropanolamine, an organic liquid COS absorbent which absorbent converts by hydrolysis the COS to H/sub 2/S and CO/sub 2/.

  9. Membrane separation of hydrocarbons

    DOEpatents

    Chang, Y. Alice; Kulkarni, Sudhir S.; Funk, Edward W.

    1986-01-01

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

  10. Direct hydrocarbon fuel cells

    DOEpatents

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

    2010-05-04

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

  11. FROZEN HYDROCARBONS IN COMETS

    SciTech Connect

    Simonia, Irakli

    2011-02-15

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

  12. Biogeochemistry of Halogenated Hydrocarbons

    NASA Astrophysics Data System (ADS)

    Adriaens, P.; Gruden, C.; McCormick, M. L.

    2003-12-01

    Halogenated hydrocarbons originate from both natural and industrial sources. Whereas direct anthropogenic emissions to the atmosphere and biosphere are often easy to assess, particularly when they are tied to major industrial activities, the attribution of emissions to other human activities (e.g., biomass burning), diffuse sources (e.g., atmospheric discharge, run off), and natural production (e.g., soils, fungi, algae, microorganisms) are difficult to quantify. The widespread occurrence of both alkyl and aryl halides in groundwater, surface water, soils, and various trophic food chains, even those not affected by known point sources, suggests a substantial biogeochemical cycling of these compounds (Wania and Mackay, 1996; Adriaens et al., 1999; Gruden et al., 2003). The transport and reactive fate mechanisms controlling their reactivity are compounded by the differences in sources of alkyl-, aryl-, and complex organic halides, and the largely unknown impact of biogenic processes, such as enzymatically mediated halogenation of organic matter, fungal production of halogenated hydrocarbons, and microbial or abiotic transformation reactions (e.g., Asplund and Grimvall, 1991; Gribble, 1996; Watling and Harper, 1998; Oberg, 2002). The largest source may be the natural halogenation processes in the terrestrial environment, as the quantities detected often exceed the amount that can be explained by human activities in the surrounding areas ( Oberg, 1998). Since biogeochemical processes result in the distribution of a wide range of halogenated hydrocarbon profiles, altered chemical structures, and isomer distributions in natural systems, source apportionment (or environmental forensics) can often only be resolved using multivariate statistical methods (e.g., Goovaerts, 1998; Barabas et al., 2003; Murphy and Morrison, 2002).This chapter will describe the widespread occurrence of halogenated hydrocarbons, interpret their distribution and biogeochemical cycling in light of

  13. THERMOCHEMISTRY OF HYDROCARBON RADICALS

    SciTech Connect

    Kent M. Ervin, Principal Investigator

    2004-08-17

    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.

  14. Radical scavengers from heavy hydrocarbons

    SciTech Connect

    Kubo, Junichi

    1996-10-01

    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.

  15. Removal of surfactants from hydrocarbons with alcohol

    SciTech Connect

    Aiello, R.P.; Poling, D.E.; Stefanidakis, G.

    1984-02-07

    A method is disclosed for removing hydrocarbon-soluble anionic surfactants from gasoline or kerosene boiling range hydrocarbons. The method comprises (a) contacting a hydrocarbon mixture containing surfactants with a lower alcohol which is miscible with the hydrocarbon mixture to extract the surfactants; (b) contacting the mixture with water or caustic solution to extract the lower alcohol and surfactants from the hydrocarbon mixture; (c) separating the water or caustic solution from the hydrocarbons; and (d) removing the hydrocarbons.

  16. Remote detection of hydrocarbon seeps

    SciTech Connect

    Barringer, A. R.

    1985-05-14

    A method of detecting hydrocarbon seeps in a sea or in earth is disclosed. The method involves interrogating aerosols formed above the sea or earth surface with an intense beam of primary light radiation generated aboard an aircraft or other vehicle. The spectral composition of the beam is selected to induce secondary light radiation in certain hydrocarbon materials contained in aerosols generated by hydrocarbon seeps rising to the sea or earth surface. The secondary light radiation is detected aboard the aircraft and subjected to spectral analysis to determine whether the composition of the aerosols is characteristic of aerosols generated by hydrocarbon seeps. Apparatus for implementing the method is also disclosed.

  17. Process for separating an ethylenically unsaturated hydrocarbon from a hydrocarbon mixture

    SciTech Connect

    vanEijl, A.T.

    1986-06-24

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

  18. Process for extracting hydrocarbons from hydrocarbon bearing ores

    SciTech Connect

    Friedman, R.H.; Eakin, B.E.

    1986-02-18

    This patent describes a process for recovering hydrocarbons from a diatomite ore consisting of: reducing the size of the ore to less than about 5 mesh to form a reduced ore; combining the reduced ore with liquid to form ore pellets; treating the ore pellets to form extractable ore pellets; contacting a bed of the extractable pellets with extracting solvent in an extraction zone such that the relative velocity of the solvent to the extractable pellets is at least about one-half gallon per square foot per minute or more to thereby extract hydrocarbons from the extractable pellets and form spent pellets and a hydrocarbon rich solvent stream comprising extracting solvent and extracted hydrocarbons. The extracted hydrocarbons have an ash content of about less than 3 weight percent; and recovering extracting solvent from the spent pellets while retaining the spent pellets in pellet form without release of a significant amount of fines.

  19. Thermophysical Properties of Hydrocarbon Mixtures

    National Institute of Standards and Technology Data Gateway

    SRD 4 NIST Thermophysical Properties of Hydrocarbon Mixtures (PC database for purchase)   Interactive computer program for predicting thermodynamic and transport properties of pure fluids and fluid mixtures containing up to 20 components. The components are selected from a database of 196 components, mostly hydrocarbons.

  20. Volatile Hydrocarbon Pheromones from Beetles

    Technology Transfer Automated Retrieval System (TEKTRAN)

    This chapter reviews literature about hydrocarbons from beetles that serve as long-range pheromones. The most thoroughly studied beetles that use volatile hydrocarbon pheromones belong to the family Nitidulidae in the genera Carpophilus and Colopterus. Published pheromone research deals with behav...

  1. Hydrocarbon sensors and materials therefor

    DOEpatents

    Pham, Ai Quoc; Glass, Robert S.

    2000-01-01

    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.

  2. Diterpenoid tetracyclic hydrocarbons of petroleum

    SciTech Connect

    Vorob'eva, N.S.; Zemskova, Z.K.; Pekh, T.I.; Petrov, A.A.

    1987-08-01

    Diterpenoid hydrocarbons are fairly widespread in various caustobioliths. However, if petroleums contain mainly acyclic diterpenoids (phytane, pristane and norpristane), cyclic diterpaenes such as fichtelite, pimarane, iosene (kaurane) and hibbane are often found in hydrocarbons isolated from coal and shale. Recent advances in the chemistry of diterpenoids isolated from caustobioliths, are described in a separate paper. Much less is known about petroleum polycyclic diterpenoid hydrocarbons, particularly those with four saturated rings. A series of tetracyclic hydrocarbons C/sub 19/H/sub 32/ (molar mass 260), found in a number of light petroleums and gas condensates from the Jura deposits of Central Kara-Kum (Turkmen S.S.R.), are examined here. These hydrocarbons are present in petroleums and condensates from the Davaly, Erden, Ortakak, Southern Beuideshik deposits, they are always identical and occur in the same ratios. The composition of the tretracyclanes isolated from the Ortakak gas condensates (well 17) will be examined in detail.

  3. Process for recovering hydrocarbons from a hydrocarbon-bearing formation

    SciTech Connect

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

    1980-03-11

    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.

  4. Hydrocarbons in Washington coastal sediments

    NASA Astrophysics Data System (ADS)

    Prahl, Fredrick G.; Carpenter, Roy

    1984-06-01

    The sources and distributions of polycyclic aromatic hydrocarbons (PAH) and aliphatic hydrocarbons are characterized in seventeen sediments from a highly river-influenced sedimentary environment off the southwestern coast of Washington. The major hydrocarbons are land-derived, introduced as preformed compounds and display long-term stability in sediment cores. A series of PAH of anthropogenic origin and two naturally derived compounds, retene and perylene, dominate the PAH composition in these sediments. Plantwax n-alkanes are the major aliphatic hydrocarbon constituents. Aliphatic hydrocarbons of marine origin, pristane and a series of four acyclic, multibranched C 25 polyolefins, are also observed in many sediments. The concentrations of these marine-derived hydrocarbons decrease to negligible levels rapidly with sediment depth from the sea-sediment interface, suggesting degradation. In general, the major land-derived hydrocarbons are concentrated in the midshelf silt deposit which extends northwestward along the continental shelf from the Columbia River mouth. A quantitatively more minor, natural series of phenanthrene homologs, also of terrestrial origin, is preferentially advected further offshore and deposited in continental slope sediments. These distributions are consistent with recognized particle associations for these compounds and sediment dispersal processes in this coastal environment. Sediment core records suggest the present pattern of dispersal has persisted for at least the past century and possibly since the Late Pleistocene.

  5. Uncertainties in hydrocarbon charge prediction

    NASA Astrophysics Data System (ADS)

    Visser, W.; Bell, A.

    Computer simulations allow the prediction of hydrocarbon volumes, composition and charge timing in undrilled petroleum prospects. Whereas different models may give different hydrocarbon charge predictions, it has now become evident that a dominant cause of erroneous predictions is the poor quality of input data. The main culprit for prediction errors is the uncertainty in the initial hydrogen index (H/C) of the source rock. A 10% uncertainty in the H/C may lead to 50% error in the predicted hydrocarbon volumes, and associated gas-oil ratio. Similarly, uncertainties in the maximum burial temperature and the kinetics of hydrocarbon generation may lead to 20-50% error. Despite this, charge modelling can have great value for the ranking of prospects in the same area with comparable geological histories.

  6. Hydrocarbon potential of Morocco

    SciTech Connect

    Achnin, H.; Nairn, A.E.M.

    1988-08-01

    Morocco lies at the junction of the African and Eurasian plates and carries a record of their movements since the end of the Precambrian. Four structural regions with basins and troughs can be identified: Saharan (Tarfaya-Ayoun and Tindouf basins); Anti-Atlas (Souss and Ouarzazate troughs and Boudnib basin); the Essaouria, Doukkala, Tadla, Missour, High Plateau, and Guercif basins; and Meseta and Rif (Rharb and Pre-Rif basins). The targets in the Tindouf basin are Paleozoic, Cambrian, Ordovician (clastics), Devonian (limestones), and Carboniferous reservoirs sourced primarily by Silurian shales. In the remaining basins, excluding the Rharb, the reservoirs are Triassic detritals, limestones at the base of the Lias and Dogger, Malm detritals, and sandy horizons in the Cretaceous. In addition to the Silurian, potential source rocks include the Carboniferous and Permo-Carboniferous shales and clays; Jurassic shales, marls, and carbonates; and Cretaceous clays. In the Rharb basin, the objectives are sand lenses within the Miocene marls. The maturation level of the organic matter generally corresponds to oil and gas. The traps are stratigraphic (lenses and reefs) and structural (horsts and folds). The seals in the pre-Jurassic rocks are shales and evaporites; in the younger rocks, shales and marl. Hydrocarbon accumulations have been found in Paleozoic, Triassic, Liassic, Malm, and Miocene rocks.

  7. Evaluation of hydrocarbon potential

    SciTech Connect

    Cashman, P.H.; Trexler, J.H. Jr.

    1992-09-30

    Task 8 is responsible for assessing the hydrocarbon potential of the Yucca Mountain vincinity. Our main focus is source rock stratigraphy in the NTS area in southern Nevada. (In addition, Trexler continues to work on a parallel study of source rock stratigraphy in the oil-producing region of east central Nevada, but this work is not funded by Task 8.) As a supplement to the stratigraphic studies, we are studying the geometry and kinematics of deformation at NTS, particularly as these pertain to reconstructing Paleozoic stratigraphy and to predicting the nature of the Late Paleozoic rocks under Yucca Mountain. Our stratigraphic studies continue to support the interpretation that rocks mapped as the {open_quotes}Eleana Formation{close_quotes} are in fact parts of two different Mississippian units. We have made significant progress in determining the basin histories of both units. These place important constraints on regional paleogeographic and tectonic reconstructions. In addition to continued work on the Eleana, we plan to look at the overlying Tippipah Limestone. Preliminary TOC and maturation data indicate that this may be another potential source rock.

  8. Illite and hydrocarbon exploration

    PubMed Central

    Pevear, David R.

    1999-01-01

    Illite is a general term for the dioctahedral mica-like clay mineral common in sedimentary rocks, especially shales. Illite is of interest to the petroleum industry because it can provide a K-Ar isotope date that constrains the timing of basin heating events. It is critical to establish that hydrocarbon formation and migration occurred after the formation of the trap (anticline, etc.) that is to hold the oil. Illite also may precipitate in the pores of sandstone reservoirs, impeding fluid flow. Illite in shales is a mixture of detrital mica and its weathering products with diagenetic illite formed by reaction with pore fluids during burial. K-Ar ages are apparent ages of mixtures of detrital and diagenetic end members, and what we need are the ages of the end members themselves. This paper describes a methodology, based on mineralogy and crystallography, for interpreting the K-Ar ages from illites in sedimentary rocks and for estimating the ages of the end members. PMID:10097055

  9. Aliphatic hydrocarbons of the fungi.

    NASA Technical Reports Server (NTRS)

    Weete, J. D.

    1972-01-01

    Review of studies of aliphatic hydrocarbons which have been recently detected in the spores of phytopathogenic fungi, and are found to be structurally very similar to the alkanes of higher plants. It appears that the hydrocarbon components of the few mycelial and yeast forms reported resemble the distribution found in bacteria. The occurence and distribution of these compounds in the fungi is discussed. Suggested functional roles of fungal spore alkanes are presented.

  10. Bioassay of polycyclic aromatic hydrocarbons

    SciTech Connect

    Van Kirk, E.A.

    1980-08-01

    A positive relationship was found between the photodynamic activity of 24 polycyclic aromatic hydrocarbons versus published results on the mutagenicity, carcinogenicity, and initiation of unscheduled DNA synthesis. Metabolic activation of benzo(a)pyrene resulted in detection of increased mutagenesis in Paramecium tetraurelia as found also in the Ames Salmonella assay. The utility of P. tetraurelia as a biological detector of hazardous polycyclic aromatic hydrocarbons is discussed.

  11. Polycyclic Aromatic Hydrocarbons

    NASA Technical Reports Server (NTRS)

    Salama, Farid

    2010-01-01

    Carbonaceous materials play an important role in space. Polycyclic Aromatic Hydrocarbons (PAHs) are a ubiquitous component of the carbonaceous materials. PAHs are the best-known candidates to account for the IR emission bands. They are also thought to be among the carriers of the diffuse interstellar absorption bands (DIBs). PAH ionization states reflect the ionization balance of the medium while PAH size, composition, and structure reflect the energetic and chemical history of the medium. A major challenge is to reproduce in the laboratory the physical conditions that exist in the emission and absorption interstellar zones. The harsh physical conditions of the ISM -low temperature, collisionless, strong UV radiation fields- are simulated in the laboratory by associating a molecular beam with an ionizing discharge to generate a cold plasma expansion. PAH ions and radicals are formed from the neutral precursors in an isolated environment at low temperature and probed with high-sensitivity cavity ringdown spectroscopy in the NUV-NIR range. Carbon nanoparticles are also formed during the short residence time of the precursors in the plasma and are characterized with time-offlight mass spectrometry. These experiments provide unique information on the spectra of large carbonaceous molecules and ions in the gas phase that can now be directly compared to interstellar and circumstellar observations (IR emission bands, DIBs, extinction curve). These findings also hold great potential for understanding the formation process of interstellar carbonaceous grains. We will review recent progress in the experimental and theoretical studies of PAHs, compare the laboratory data with astronomical observations and discuss the global implications.

  12. Enrichment of light hydrocarbon mixture

    SciTech Connect

    Yang; Dali; Devlin, David; Barbero, Robert S.; Carrera, Martin E.; Colling, Craig W.

    2010-08-10

    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.

  13. Enrichment of light hydrocarbon mixture

    DOEpatents

    Yang, Dali; Devlin, David; Barbero, Robert S.; Carrera, Martin E.; Colling, Craig W.

    2011-11-29

    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.

  14. Hydrocarbon components in carbonaceous meteorites

    NASA Astrophysics Data System (ADS)

    Kissin, Y. V.

    2003-05-01

    Currently, the presence of free n-alkanes and isoprenoid alkanes in carbonaceous meteorites is usually explained either by microbial contamination during the period between the meteorite fall and collection or by contamination from the environment of analytical laboratories and museums. The goal of this research was to repeat analysis of hydrocarbon components in meteorites and to investigate possible meteorite contamination routes discussed in the literature. Experimental analysis of free organic constituents in five carbonaceous meteorites by infrared spectroscopy (IR) and gas chromatographic (GC) methods confirmed the presence of extractable aliphatic components, n-alkanes in the C 15H 32-C 27H 56 range and isoprenoid alkanes (phytane, pristane, and norpristane), in some of these meteorites. The contents of these compounds vary depending on the source. Insoluble organic components of two meteorites (meteorite kerogens) were isolated, and their composition was analyzed by IR and cracking/GC methods. Comparison with the data on several terrestrial contamination sources proposed in the literature shows that the presence of free saturated hydrocarbons in meteorites and the composition of the meteorite kerogen could not be explained either by microbial contamination or by contamination from the laboratory environment. The types of the hydrocarbons in meteorites resemble those typical of ancient terrestrial deposits of organic-rich sediments, except for the absence of lighter hydrocarbons, which apparently slowly evaporated in space, and multi-ring naphthenic compounds of the biologic origin, steranes, terpanes, etc. The prevailing current explanation for the presence of free linear saturated hydrocarbons in carbonaceous meteorites, apart from contamination, is the abiotic route from hydrogen and carbon monoxide. However, the data on the structure of meteorite kerogens require a search for different routes that initially produce complex polymeric structures containing

  15. Process for purification of hydrocarbons

    SciTech Connect

    Chao, C.C.; Rastelli, H.

    1991-05-28

    This patent describes a process for separating a minor proportion of ammonia form a hydrocarbon having a kinetic diameter of not more than about 5 {Angstrom}. It comprises: contacting a feedstream comprising ammonia and the hydrocarbon with clinoptilolite that has been subjected to ion-exchange with at least one metal cation of the group consisting of lithium, sodium, potassium, calcium, magnesium, barium and strontium, zinc, copper, cobalt, iron and manganese cations to an extent sufficient to cause the ammonia to be selectively absorbed into the clinoptilolite and withdrawing a product stream at least partially depleted in ammonia relative to the feedstream.

  16. Method for producing viscous hydrocarbons

    DOEpatents

    Poston, Robert S.

    1982-01-01

    A method for recovering viscous hydrocarbons and synthetic fuels from a subterranean formation by drilling a well bore through the formation and completing the well by cementing a casing means in the upper part of the pay zone. The well is completed as an open hole completion and a superheated thermal vapor stream comprised of steam and combustion gases is injected into the lower part of the pay zone. The combustion gases migrate to the top of the pay zone and form a gas cap which provides formation pressure to produce the viscous hydrocarbons and synthetic fuels.

  17. Biological enhancement of hydrocarbon extraction

    DOEpatents

    Brigmon, Robin L.; Berry, Christopher J.

    2009-01-06

    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.

  18. Hydrocarbon and chlorinated hydrocarbon-soluble magnesium dialkoxides

    SciTech Connect

    Kamienski, C.W.

    1988-05-31

    This patent describes a process for the preparation of hydrocarbon or chlorinated hydrocarbon solvent solutions of magnesium dialkoxides, which comprises reacting a suspension of magnesium metal or magnesium amide, or a solution of a dialkyimagnesium compound, in a volatile hydrocarbon or chlorinated hydrocarbon solvent with an alcohol selected from the group of (a) aliphatic, cycloaliphatic and acyclic C/sub 5/-C/sub 18/ beta- and gamma-alkyl-substituted secondary and tertiary monohydric alcohols; or (b) mixtures of the (a) alcohols with C/sub 3/-C/sub 18/ aliphatic or cycloaliphatic beta- and gamma-alkyl-unsubstituted secondary or tertiary alcohols; or (c) mixtures of the (a) alcohols with C/sub 1/-C/sub 18/ aliphatic primary unsubstituted and 2-alkyl-substituted alcohols; the mole ratios of the (a) to the (b), and the (a) to the (c), alcohols being 1 of the (a) alcohols to 0.1 to 2 of the (b) and/or the (c) alcohols.

  19. FUNGI AND HYDROCARBONS IN THE MARINE ENVIRONMENT

    EPA Science Inventory

    Hydrocarbons from various sources--anthropogenic pollution, marine seeps, marine algae, atmospheric fallout and terrestrial runoff--enter the ocean daily. These complex hydrocarbon mixtures are dispersed and degraded by abiotic and biogenic processes. Most commonly, bacteria are ...

  20. THE PHOTOTOXICITY OF POLYCYCLIC AROMATIC HYDROCARBONS

    EPA Science Inventory

    The U.S. Environmental Protection Agency (EPA) continues to be interested in developing methods for the detection of polycyclic aromatic hydrocarbons (PAHS) in the environment. Polycyclic aromatic hydrocarbons (PAHS) are common contaminants in our environment. Being major product...

  1. PASSENGER CAR HYDROCARBON EMISSIONS SPECIATION

    EPA Science Inventory

    Emission factors for over 60 individual hydrocarbon compounds were determined for four passenger cars. The cars included a 1963 Chevrolet, a 1977 Mustang, and 1978 Monarch, and 1979 LTD II. The speciation data is reported for both tailpipe and evaporative emissions. The tailpipe ...

  2. HYDROCARBON SPILL EXPOSURE ASSESSMENT MODELING

    EPA Science Inventory

    Hydrocarbon spills impact drinking water supplies at down gradient locations. onventional finite difference and finite element models of multiphase, multicomponent flow have extreme requirements for both computer time and site data. ite data and the intent of the modeling often d...

  3. Steam Hydrocarbon Cracking and Reforming

    ERIC Educational Resources Information Center

    Golombok, Michael

    2004-01-01

    The interactive methods of steam hydrocarbon reforming and cracking of the oil and chemical industries are scrutinized, with special focus on their resemblance and variations. The two methods are illustrations of equilibrium-controlled and kinetically-controlled processes, the analysis of which involves theories, which overlap and balance each…

  4. Hydrocarbons from plants and trees

    SciTech Connect

    Calvin, M.

    1982-07-01

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

  5. Measurement of Hydrocarbon Transport in Bacteria

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Hydrocarbon uptake by bacteria has not been extensively studied, and strong evidence for active transport of hydrocarbons is lacking. The volatile nature of hydrocarbons, their hydrophobicity, and their relatively low aqueous solubilities can complicate transport assays. Here we present a detailed...

  6. Biodegradation of petroleum hydrocarbons in hypersaline environments.

    PubMed

    Martins, Luiz Fernando; Peixoto, Raquel Silva

    2012-07-01

    Literature on hydrocarbon degradation in extreme hypersaline media presents studies that point to a negative effect of salinity increase on hydrocarbonoclastic activity, while several others report an opposite tendency. Based on information available in the literature, we present a discussion on the reasons that justify these contrary results. Despite the fact that microbial ability to metabolize hydrocarbons is found in extreme hypersaline media, indeed some factors are critical for the occurrence of hydrocarbon degradation in such environments. How these factors affect hydrocarbon degradation and their implications for the assessment of hydrocarbon biodegradation in hypersaline environments are presented in this review. PMID:24031900

  7. Syngas Upgrading to Hydrocarbon Fuels Technology Pathway

    SciTech Connect

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

    2013-03-01

    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.

  8. Biodegradation of petroleum hydrocarbons in hypersaline environments

    PubMed Central

    Martins, Luiz Fernando; Peixoto, Raquel Silva

    2012-01-01

    Literature on hydrocarbon degradation in extreme hypersaline media presents studies that point to a negative effect of salinity increase on hydrocarbonoclastic activity, while several others report an opposite tendency. Based on information available in the literature, we present a discussion on the reasons that justify these contrary results. Despite the fact that microbial ability to metabolize hydrocarbons is found in extreme hypersaline media, indeed some factors are critical for the occurrence of hydrocarbon degradation in such environments. How these factors affect hydrocarbon degradation and their implications for the assessment of hydrocarbon biodegradation in hypersaline environments are presented in this review. PMID:24031900

  9. Hydrocarbon Rocket Technology Impact Forecasting

    NASA Technical Reports Server (NTRS)

    Stuber, Eric; Prasadh, Nishant; Edwards, Stephen; Mavris, Dimitri N.

    2012-01-01

    Ever since the Apollo program ended, the development of launch propulsion systems in the US has fallen drastically, with only two new booster engine developments, the SSME and the RS-68, occurring in the past few decades.1 In recent years, however, there has been an increased interest in pursuing more effective launch propulsion technologies in the U.S., exemplified by the NASA Office of the Chief Technologist s inclusion of Launch Propulsion Systems as the first technological area in the Space Technology Roadmaps2. One area of particular interest to both government agencies and commercial entities has been the development of hydrocarbon engines; NASA and the Air Force Research Lab3 have expressed interest in the use of hydrocarbon fuels for their respective SLS Booster and Reusable Booster System concepts, and two major commercially-developed launch vehicles SpaceX s Falcon 9 and Orbital Sciences Antares feature engines that use RP-1 kerosene fuel. Compared to engines powered by liquid hydrogen, hydrocarbon-fueled engines have a greater propellant density (usually resulting in a lighter overall engine), produce greater propulsive force, possess easier fuel handling and loading, and for reusable vehicle concepts can provide a shorter turnaround time between launches. These benefits suggest that a hydrocarbon-fueled launch vehicle would allow for a cheap and frequent means of access to space.1 However, the time and money required for the development of a new engine still presents a major challenge. Long and costly design, development, testing and evaluation (DDT&E) programs underscore the importance of identifying critical technologies and prioritizing investment efforts. Trade studies must be performed on engine concepts examining the affordability, operability, and reliability of each concept, and quantifying the impacts of proposed technologies. These studies can be performed through use of the Technology Impact Forecasting (TIF) method. The Technology Impact

  10. Kinetic models of hydrocarbon generation

    SciTech Connect

    Burnham, A.K.; Sweeney, J.J.

    1990-10-25

    We are carrying out an integrated program of laboratory experiments, kinetics modeling, and basin thermal history modeling in order to better understand the natural breakdown of organic matter into oil and gas. Our kinetic models of organic maturation are being used to better understand the coupling of generation, cracking, expulsion, and overpressuring in both the laboratory and geologic setting. Currently we are carrying out chemical experiments and developing more efficient chemical kinetic modeling schemes to obtain a better understanding of expulsion and cracking from lean source rocks and from hydrogen-poor (terrestrial) organic source material. We verify the chemical kinetic models by integrating them with thermal history models of hydrocarbon-producing sediments and comparing predicted and observed characteristics of the hydrocarbon occurrence in a variety of settings. We intend to apply this approach to evaluate the potential for deep gas resources in the Pacific Northwest and in the Louisiana Gulf Coast. 11 refs., 4 figs.

  11. Dry reforming of hydrocarbon feedstocks

    SciTech Connect

    Shah, Yatish T.; Gardner, Todd H.

    2014-09-25

    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.

  12. Synfuels: Hydrocarbons of the future

    SciTech Connect

    Matar, S.

    1982-09-01

    The author reviews Synfuels: Hydrocarbons of the Future by Sami Matar (discusses the important chemical advances made in the synfuels industry and the opportunities available for artificially producing new fuels) and Lighting Energy Management for Colleges and Universities from the National Lighting Bureau and the Energy Task Force (gives information on conducting a lighting energy audit, calculating lighting expenses and savings, and a glossary of terms).

  13. Catalytic method for synthesizing hydrocarbons

    DOEpatents

    Sapienza, Richard S.; Sansone, Michael J.; Slegeir, William A. R.

    1984-01-01

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

  14. Catalytic method for synthesizing hydrocarbons

    DOEpatents

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

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

  15. Underground caverns for hydrocarbon storage

    SciTech Connect

    Barron, T.F.

    1998-12-31

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

  16. Deep desulfurization of hydrocarbon fuels

    DOEpatents

    Song, Chunshan; Ma, Xiaoliang; Sprague, Michael J.; Subramani, Velu

    2012-04-17

    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.

  17. Abnormal pressure in hydrocarbon environments

    USGS Publications Warehouse

    Law, B.E.; Spencer, C.W.

    1998-01-01

    Abnormal pressures, pressures above or below hydrostatic pressures, occur on all continents in a wide range of geological conditions. According to a survey of published literature on abnormal pressures, compaction disequilibrium and hydrocarbon generation are the two most commonly cited causes of abnormally high pressure in petroleum provinces. In young (Tertiary) deltaic sequences, compaction disequilibrium is the dominant cause of abnormal pressure. In older (pre-Tertiary) lithified rocks, hydrocarbon generation, aquathermal expansion, and tectonics are most often cited as the causes of abnormal pressure. The association of abnormal pressures with hydrocarbon accumulations is statistically significant. Within abnormally pressured reservoirs, empirical evidence indicates that the bulk of economically recoverable oil and gas occurs in reservoirs with pressure gradients less than 0.75 psi/ft (17.4 kPa/m) and there is very little production potential from reservoirs that exceed 0.85 psi/ft (19.6 kPa/m). Abnormally pressured rocks are also commonly associated with unconventional gas accumulations where the pressuring phase is gas of either a thermal or microbial origin. In underpressured, thermally mature rocks, the affected reservoirs have most often experienced a significant cooling history and probably evolved from an originally overpressured system.

  18. HYDROCARBON AND SULFUR SENSORS FOR SOFC SYSTEMS

    SciTech Connect

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

    2003-11-01

    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.

  19. AUTOMOTIVE HYDROCARBON EMISSION PATTERNS AND THE MEASUREMENT OF NONMETHANE HYDROCARBON EMISSION RATES

    EPA Science Inventory

    The advent of emission control technology has resulted in significant changes in both the total mass and detailed patterns of hydrocarbons emitted from automobiles. Emission rates of 56 hydrocarbons from 22 motor vehicles, including catalyst and noncatalyst configurations, were d...

  20. New technique for calibrating hydrocarbon gas flowmeters

    NASA Technical Reports Server (NTRS)

    Singh, J. J.; Puster, R. L.

    1984-01-01

    A technique for measuring calibration correction factors for hydrocarbon mass flowmeters is described. It is based on the Nernst theorem for matching the partial pressure of oxygen in the combustion products of the test hydrocarbon, burned in oxygen-enriched air, with that in normal air. It is applied to a widely used type of commercial thermal mass flowmeter for a number of hydrocarbons. The calibration correction factors measured using this technique are in good agreement with the values obtained by other independent procedures. The technique is successfully applied to the measurement of differences as low as one percent of the effective hydrocarbon content of the natural gas test samples.

  1. Vaporization and gasification of hydrocarbon feedstocks

    SciTech Connect

    Davies, H.S.; Garstang, J.H.; Timmins, C.

    1983-08-23

    Heavy hydrocarbon feedstocks, e.g. gas oils, are vaporized and subsequently gasified at high temperatures without pyrolytic degradation by first admixing the hydrocarbon with a hot gaseous reactant, e.g. product gas or steam, to bring the temperature of the mixture above that of the dew point of the hydrocarbon and thereafter raising the temperature of the mixture to above that at which pyrolysis of the hydrocarbon begins to be significant by admixture with further quantities of the reactant which are superheated thereby to bring the temperature of the resultant mixture to that required for effecting a catalytic gasification reaction.

  2. Spreading coefficients of aliphatic hydrocarbons on water

    SciTech Connect

    Takii, Taichi; Mori, Y.H. . Dept. of Mechanical Engineering)

    1993-11-01

    Experiments have been performed to determine the equilibrium spreading coefficients of some aliphatic hydrocarbons (C[sub 6]C[sub 10]) on water. The thickness of a discrete lens of each hydrocarbon sample floating on a stagnant water pool was measured interferometrically and used to calculate the spreading coefficient of the hydrocarbon with the aid of Langmuir's capillarity theory. The dependences of the spreading coefficient, thus observed, on temperature (0--50 C) and on the number of carbon atoms in the hydrocarbon molecule are in qualitative agreement with the predictions based on the Lifshitz theory of van der Waals forces.

  3. Nox reduction system utilizing pulsed hydrocarbon injection

    DOEpatents

    Brusasco, Raymond M.; Penetrante, Bernardino M.; Vogtlin, George E.; Merritt, Bernard T.

    2001-01-01

    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.

  4. Membrane separation of hydrocarbons using cycloparaffinic solvents

    DOEpatents

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

    1988-06-14

    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.

  5. Membrane separation of hydrocarbons using cycloparaffinic solvents

    DOEpatents

    Kulkarni, Sudhir S.; Chang, Y. Alice; Gatsis, John G.; Funk, Edward W.

    1988-01-01

    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.

  6. 40 CFR 86.121-90 - Hydrocarbon analyzer calibration.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 19 2012-07-01 2012-07-01 false Hydrocarbon analyzer calibration. 86... Complete Heavy-Duty Vehicles; Test Procedures § 86.121-90 Hydrocarbon analyzer calibration. The hydrocarbon... FID and HFID hydrocarbon analyzers shall be adjusted for optimum hydrocarbon response....

  7. 40 CFR 86.121-90 - Hydrocarbon analyzer calibration.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 18 2010-07-01 2010-07-01 false Hydrocarbon analyzer calibration. 86... Complete Heavy-Duty Vehicles; Test Procedures § 86.121-90 Hydrocarbon analyzer calibration. The hydrocarbon... FID and HFID hydrocarbon analyzers shall be adjusted for optimum hydrocarbon response....

  8. 40 CFR 86.121-90 - Hydrocarbon analyzer calibration.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 18 2011-07-01 2011-07-01 false Hydrocarbon analyzer calibration. 86... Complete Heavy-Duty Vehicles; Test Procedures § 86.121-90 Hydrocarbon analyzer calibration. The hydrocarbon... FID and HFID hydrocarbon analyzers shall be adjusted for optimum hydrocarbon response....

  9. 40 CFR 86.121-90 - Hydrocarbon analyzer calibration.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 19 2014-07-01 2014-07-01 false Hydrocarbon analyzer calibration. 86... Complete Heavy-Duty Vehicles; Test Procedures § 86.121-90 Hydrocarbon analyzer calibration. The hydrocarbon... FID and HFID hydrocarbon analyzers shall be adjusted for optimum hydrocarbon response....

  10. 40 CFR 86.121-90 - Hydrocarbon analyzer calibration.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 19 2013-07-01 2013-07-01 false Hydrocarbon analyzer calibration. 86... Complete Heavy-Duty Vehicles; Test Procedures § 86.121-90 Hydrocarbon analyzer calibration. The hydrocarbon... FID and HFID hydrocarbon analyzers shall be adjusted for optimum hydrocarbon response....

  11. Human Skin Aryl Hydrocarbon Hydroxylase

    PubMed Central

    Bickers, David R.; Kappas, Attallah

    1978-01-01

    Coal tar products, which are widely used in treating dermatologic disease, contain numerous polycyclic aromatic hydrocarbons, including 3,4-benzo[a]pyrene (BP). BP is among the most potent environmental chemical carcinogens and is known to evoke tumors in the skin of experimental animals and perhaps also of man. In this study the effect of cutaneous application of coal tar solution (U. S. Pharmacopeia) on aryl hydrocarbon hydroxylase (AHH) activity in the skin of patients usually treated with this drug was investigated. AHH, a cytochrome P-450 dependent carcinogen-metabolizing enzyme appears to play an important role in the activation of polycyclic hydrocarbons into reactive moieties that can bind to DNA and that may directly induce cancer. Application of coal tar solution to human skin caused a two to five-fold induction of cutaneous AHH in nine subjects. In further studies, the incubation of human skin with coal tar solution in vitro also caused variable induction of cutaneous AHH. Maximum responses in both systems occurred after 24 h and enzyme activity in vitro was time- and tissue- and substrate-concentration dependent. Studies in experimental animals showed that topical application of coal tar solution caused induction of AHH in skin and, after percutaneous absorption, in liver as well. Assay of several defined constituents of coal tar for AHH induction showed that BP was the most potent inducer of AHH tested. These studies indicate that topical application of coal tar solution in doses ordinarily used in treating dermatologic disease causes induction of AHH in human skin and suggest that such induced enzymatic activity could relate to carcinogenic responses to this agent in skin or, after percutaneous absorption, in other tissues as well. PMID:711851

  12. Hydrocarbon release investigations in Missouri

    SciTech Connect

    Fels, J.B.

    1996-09-01

    Hydrocarbon releases are among the most common environmental problems in Missouri, as well as across the country. Old, unprotected underground storage tanks and buried piping from the tanks to pumps are notorious sources of petroleum contamination at LUST (leaking underground storage tank) sites. Missouri has an estimated 5000 LUST sites across the state with the majority being simple spills into clay-rich soils or into a shallow perched water system. However, in the southern half of the state, where residual soils and karst bedrock are not conducive to trapping such releases, significant groundwater supplies are at risk. This article discusses the process used to identify the source of contamination.

  13. Biological sources for phenylalkane hydrocarbons

    SciTech Connect

    Ellis, L.; Winans, R.E.; Langworthy, T.A.; Langworthy, T.A.

    1996-12-31

    Linear alkylbenzenes (phenylalkanes) represent an important class of molecular compounds used widely in today`s society as building blocks for detergent manufacture, indeed, the almost universal widespread use and acceptance of detergents has been reflected by the fact that detergent chemical components can be found in and around almost every location around the globe where human settlements exist. This being the case, detergent chemical components represent a well recognized indicator of pollution in the lakes, rivers, and coastal water systems of the world. The identification of phenylalkane hydrocarbons in ancient sedimentary organic matter has been the subject of much controversy and concern, owing to the ubiquitous presence of phenylalkanes in today`s society. The finding of these components in the trace analytical analyses of petroleum sediments and crude oils has always implied {open_quotes}detergent contamination{close_quotes}. New evidence, however, suggests that the finding of phenylalkanes in ancient geological materials may actually represent an input from ancient algae and/or bacteria which contributed to the organic biomass from which the sediment or crude oil was derived. Moreover, the finding also of phenylalkane hydrocarbons in the lipids extracts of thermophilic bacteria still living today has revealed the first evidence of a natural system producing these compounds.

  14. 40 CFR 52.1877 - Control strategy: Photochemical oxidants (hydrocarbons).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... oxidants (hydrocarbons). 52.1877 Section 52.1877 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY....1877 Control strategy: Photochemical oxidants (hydrocarbons). (a) The requirements of Subpart G of this... national standard for photochemical oxidants (hydrocarbons) in the Metropolitan Cincinnati...

  15. 40 CFR 52.1877 - Control strategy: Photochemical oxidants (hydrocarbons).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... oxidants (hydrocarbons). 52.1877 Section 52.1877 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY....1877 Control strategy: Photochemical oxidants (hydrocarbons). (a) The requirements of Subpart G of this... national standard for photochemical oxidants (hydrocarbons) in the Metropolitan Cincinnati...

  16. 40 CFR 52.1877 - Control strategy: Photochemical oxidants (hydrocarbons).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... oxidants (hydrocarbons). 52.1877 Section 52.1877 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY....1877 Control strategy: Photochemical oxidants (hydrocarbons). (a) The requirements of Subpart G of this... national standard for photochemical oxidants (hydrocarbons) in the Metropolitan Cincinnati...

  17. 40 CFR 52.1877 - Control strategy: Photochemical oxidants (hydrocarbons).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... oxidants (hydrocarbons). 52.1877 Section 52.1877 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY....1877 Control strategy: Photochemical oxidants (hydrocarbons). (a) The requirements of Subpart G of this... national standard for photochemical oxidants (hydrocarbons) in the Metropolitan Cincinnati...

  18. 40 CFR 52.1877 - Control strategy: Photochemical oxidants (hydrocarbons).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... oxidants (hydrocarbons). 52.1877 Section 52.1877 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY....1877 Control strategy: Photochemical oxidants (hydrocarbons). (a) The requirements of Subpart G of this... national standard for photochemical oxidants (hydrocarbons) in the Metropolitan Cincinnati...

  19. Conversion of organic solids to hydrocarbons

    DOEpatents

    Greenbaum, E.

    1995-05-23

    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.

  20. Conversion of organic solids to hydrocarbons

    DOEpatents

    Greenbaum, Elias

    1995-01-01

    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.

  1. An Easy Synthesis of Two Cage Hydrocarbons.

    ERIC Educational Resources Information Center

    Dong, Dao Cong

    1982-01-01

    Describes a simple, three-step synthesis of two cage molecules, birdcage hydrocarbon (VIII) and its homologue, the homobirdcage hydrocarbon IX. Indicates that all products are easily purified and formed in high yields in this activity suitable for advanced undergraduate laboratory courses. (Author/JN)

  2. Microbial degradation of hydrocarbons in the environment.

    PubMed Central

    Leahy, J G; Colwell, R R

    1990-01-01

    The ecology of hydrocarbon degradation by microbial populations in the natural environment is reviewed, emphasizing the physical, chemical, and biological factors that contribute to the biodegradation of petroleum and individual hydrocarbons. Rates of biodegradation depend greatly on the composition, state, and concentration of the oil or hydrocarbons, with dispersion and emulsification enhancing rates in aquatic systems and absorption by soil particulates being the key feature of terrestrial ecosystems. Temperature and oxygen and nutrient concentrations are important variables in both types of environments. Salinity and pressure may also affect biodegradation rates in some aquatic environments, and moisture and pH may limit biodegradation in soils. Hydrocarbons are degraded primarily by bacteria and fungi. Adaptation by prior exposure of microbial communities to hydrocarbons increases hydrocarbon degradation rates. Adaptation is brought about by selective enrichment of hydrocarbon-utilizing microorganisms and amplification of the pool of hydrocarbon-catabolizing genes. The latter phenomenon can now be monitored through the use of DNA probes. Increases in plasmid frequency may also be associated with genetic adaptation. Seeding to accelerate rates of biodegradation has been shown to be effective in some cases, particularly when used under controlled conditions, such as in fermentors or chemostats. PMID:2215423

  3. Hydrocarbon distribution in the Maracaibo Basin

    SciTech Connect

    Scherer, W.

    1996-08-01

    The prolific Maracaibo basin contains the second largest hydrocarbon accumulation in South America; it has been one of the principal oil producers of the world since the beginning of this century. Exploratory efforts in this basin, carried out with new techniques and new ideas, continue today, so it is of interest to determine the trends of hydrocarbon concentrations in terms of resources per unit volume of sediments and to correlate them to stratigraphic, sedimentary-tectonic and geochemical variables. Regional scale maps representing the 24 principal geologic and geochemical variables that are thought to be a function of hydrocarbon generation, migration and accumulation were discretized on a 25 x 25 km grid. Variables used are isopach and Total Organic Carbon (TOC) of source rocks, isopach, sandstone content and grain size parameters of reservoir rocks, isopach of stratigraphic seal and overburden, maximum paleotemperatures (R{sub o} and T{sub max}), tectonic energy (fault length and displacement) and hydrocarbon families. Multivariate analytical statistics was used to obtain the trends of hydrocarbon distributions. The resulting hydrocarbon concentration trend map was quantitatively correlated to known hydrocarbon accumulations and prospective areas, where additional new accumulations might be found, were obtained. It can be shown that the largest known hydrocarbon concentrations correspond to areas of greatest cumulative overburden. The southern Zulia Catatumbo region is the largest prospective area determined by this method.

  4. Polynuclear aromatic hydrocarbons for fullerene synthesis in flames

    DOEpatents

    Alford, J. Michael; Diener, Michael D.

    2006-12-19

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

  5. Effect of gasoline composition on exhaust hydrocarbon

    SciTech Connect

    Kameoka, Atsushi; Akiyama, Ken-ichi; Hosoi, Kenzo

    1994-10-01

    The purpose of this study is to evaluate the characteristics of individual hydrocarbons in gasoline and to clarify the effect of the gasoline composition on engine-out exhaust hydrocarbons. Experiments were performed on a single cylinder research engine operating under steady state condition. The test fuels were blended gasolines of alkylate, catalytic reformate and fluid catalytic cracking gasoline. Chemically defined binary fuel mixtures of isooctane, benzene, toluene, xylene, and ethylbenzene were used as variables to study their impact on exhaust hydrocarbons. The individual exhaust hydrocarbon species were analyzed using a gas chromatograph with flame ionization detector. The results of tests with blended gasoline indicated that the exhaust hydrocarbons were classified into the unburned fuel and the cracked products such as methane, ethane and various olefins. The production coefficients of benzene were 5% for toluene, 4% for xylene and 6% for ethylbenzene. These values suggested that alkylbenzene in the fuel produced benzene in the exhaust. 8 refs., 16 figs., 5 tabs.

  6. Hydrocarbonates in precipitation of Moscow

    NASA Astrophysics Data System (ADS)

    Larin, Igor; Eremina, Iren; Aloyan, Artash; Arutunan, Vardan; Chubarova, Natalia; Yermakov, Alexandr

    2016-04-01

    According to monitoring of the atmospheric precipitation of Moscow a number of episodes is revealed, the content of hydrocarbonates in which repeatedly surpasses equilibrium level. Facts of their registration are linked to complex structure of precipitation which is caused by a different chemical composition of condensation nucleus. As a result on the underlying surface two groups of drops with acidity of the different nature are transferred. The acidity of the first, "metal" group of droplets, is determined by a carbonate equilibrium with atmospheric CO2 and with dissolved carbonates of alkali and alkaline earth metals. The acidity of the second, "ammonium" group droplets, is characterized by the balance between an ammonia absorbed from the air and atmospheric acids. Regulation of acidity of the deposits measured in a course of monitoring, occurs for this reason not only in the air, but also in the condensate receiver. A mixing "metal" and "ammonium" groups precipitation accompanied by only a partial transfer of hydrocarbonates in the dissolved CO2. The process is braked as a result of a practical stop of exit of CO2 into the atmosphere because of a mass transfer deceleration. In turn it leads to excess of equilibrium level of hydrocarbonates in the receiver. Estimates show that the acidity of "ammonia" component of precipitation should be much higher than the reported monitoring data. In other words, real acidity of rain drops can essentially exceed that is measured by standard procedures of monitoring of deposits, that it is necessary to take into consideration at calculations of so-called critical levels of acid loading on people and environment. In other words, the actual acidity of raindrops could greatly exceed that is measured by the standard procedures for monitoring rainfall, which should be taken into account when calculating the so-called critical levels of acid loads on people and the environment. It follows that the true level of hazard of acid rain

  7. Volatile hydrocarbons in pharmaceutical solutions

    SciTech Connect

    Kroneld, R. )

    1991-07-01

    Volatile pollutants such as hydrocarbons have, during many years, been analysed in small concentrations in air, water, food, pharmaceutical solutions, and human blood and tissues. It has also been shown that such substances have unexpected consequences for cell cultures and scientific experiments. These substances also accumulate in patients receiving haemodialysis and these patients are exposed to quite high concentrations. The knowledge of the toxicity of such compounds has led to the development of maximum limit concentrations with the aim to decrease the exposure of humans. This paper discusses the problems of human exposure in general and especially through pharmaceutical solutions, and the possibilities of eliminating such compounds with the aim of decreasing the exposure as a hygienic challenge.

  8. Remote Sensing And Surface Hydrocarbon Leakage

    NASA Astrophysics Data System (ADS)

    Matthews, M. D.; Jones, V. T.; Richers, D. M.

    1984-08-01

    The Geosat oil and gas test site program stimulated interest in the interaction between surface hydrocarbon concentrations and interpretation of remote sensing data. The test case results suggested that lineaments correspond to avenues of preferential hydrocarbon seepage and that this seepage affects vegetation health and populations at Patrick Draw field in Wyoming and potentially at Lost River field, West Virginia. These two areas were selected for additional surface hydrocarbon surveys in order to test these hypotheses. The Patrick Draw study shows that a zone of stressed vegetation, visible on thematic mapper data, definitely coincides with an area of marked leakage of hydrocarbons and that the composition of these gases would predict an intermediate type oil and gas reservoir such as exists in the area. The study further indicates that the leakage is in large part controlled by the presence of fractures/faults recognized as lineaments on the remote sensing images. The Lost River study specifically investigated the possible existence of hydrocarbon leakage causing anomalous populations of maple trees in a climax oak forest. These maples were first recognized by study of thematic mapper simulator data. The soil gas hydrocarbon concentrations are above average in several of the maple anomalies over the field. This supports the inference that the maples are present because they are more tolerant of soil conditions where hydrocarbon seepage is active. The crest of the field has low soil gas magnitudes, but high values occur to the updip eastern edge of the field along a fault/fracture that was detected in the seismic data. The conclusion that preferential pathways of hydrocarbon leakage are recognized in spectral and textural analysis of remote sensing data is supported by other studies and integrated into a suggested exploration/hydrocarbon migration model.

  9. Emulsification of hydrocarbons by subsurface bacteria

    USGS Publications Warehouse

    Francy, D.S.; Thomas, J.M.; Raymond, R.L.; Ward, C.H.

    1991-01-01

    Biosurfactants have potential for use in enhancement of in situ biorestoration by increasing the bioavailability of contaminants. Microorganisms isolated from biostimulated, contaminated and uncontaminated zones at the site of an aviation fuel spill and hydrocarbon-degrading microorganisms isolated from sites contaminated with unleaded gasoline were examined for their abilities to emulsify petroleum hydrocarbons. Emulsifying ability was quantified by a method involving agitation and visual inspection. Biostimulated-zone microbes and hydrocarbon-degrading microorganisms were the best emulsifiers as compared to contaminated and uncontaminated zone microbes. Biostimulation (nutrient and oxygen addition) may have been the dominant factor which selected for and encouraged growth of emulsifiers; exposure to hydrocarbon was also important. Biostimulated microorganisms were better emulsifiers of aviation fuel (the contaminant hydrocarbon) than of heavier hydrocarbon to which they were not previously exposed. By measuring surface tension changes of culture broths, 11 out of 41 emulsifiers tested were identified as possible biosurfactant producers and two isolates produced large surface tension reductions indicating the high probability of biosurfactant production.Biosurfactants have potential for use in enhancement of in situ biorestoration by increasing the bioavailability of contaminants. Microorganisms isolated from biostimulated, contaminated and uncontaminated zones at the site of an aviation fuel spill and hydrocarbon-degrading microorganisms isolated from sites contaminated with unleaded gasoline were examined for their abilities to emulsify petroleum hydrocarbons. Emulsifying ability was quantified by a method involving agitation and visual inspection. Biostimulated-zone microbes and hydrocarbon-degrading microorganisms were the best emulsifiers as compared to contaminated and uncontaminated zone microbes. Biostimulation (nutrient and oxygen addition) may have been

  10. Using supercritical fluids to refine hydrocarbons

    DOEpatents

    Yarbro, Stephen Lee

    2015-06-09

    A system and method for reactively refining hydrocarbons, such as heavy oils with API gravities of less than 20 degrees and bitumen-like hydrocarbons with viscosities greater than 1000 cp at standard temperature and pressure, using a selected fluid at supercritical conditions. A reaction portion of the system and method delivers lightweight, volatile hydrocarbons to an associated contacting unit which operates in mixed subcritical/supercritical or supercritical modes. Using thermal diffusion, multiphase contact, or a momentum generating pressure gradient, the contacting unit separates the reaction products into portions that are viable for use or sale without further conventional refining and hydro-processing techniques.

  11. 40 CFR 86.317-79 - Hydrocarbon analyzer specifications.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 19 2012-07-01 2012-07-01 false Hydrocarbon analyzer specifications....317-79 Hydrocarbon analyzer specifications. (a) Hydrocarbon measurements are to be made with a heated... measures hydrocarbon emissions on a dry basis is permitted for gasoline-fueled testing; Provided,...

  12. 40 CFR 86.317-79 - Hydrocarbon analyzer specifications.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 19 2013-07-01 2013-07-01 false Hydrocarbon analyzer specifications....317-79 Hydrocarbon analyzer specifications. (a) Hydrocarbon measurements are to be made with a heated... measures hydrocarbon emissions on a dry basis is permitted for gasoline-fueled testing; Provided,...

  13. 40 CFR 92.119 - Hydrocarbon analyzer calibration.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 20 2010-07-01 2010-07-01 false Hydrocarbon analyzer calibration. 92... Hydrocarbon analyzer calibration. The HFID hydrocarbon analyzer shall receive the following initial and... into service and at least annually thereafter, the HFID hydrocarbon analyzer shall be adjusted...

  14. 40 CFR 86.317-79 - Hydrocarbon analyzer specifications.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 18 2011-07-01 2011-07-01 false Hydrocarbon analyzer specifications....317-79 Hydrocarbon analyzer specifications. (a) Hydrocarbon measurements are to be made with a heated... measures hydrocarbon emissions on a dry basis is permitted for gasoline-fueled testing; Provided,...

  15. 40 CFR 92.119 - Hydrocarbon analyzer calibration.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 21 2012-07-01 2012-07-01 false Hydrocarbon analyzer calibration. 92... Hydrocarbon analyzer calibration. The HFID hydrocarbon analyzer shall receive the following initial and... into service and at least annually thereafter, the HFID hydrocarbon analyzer shall be adjusted...

  16. 21 CFR 178.3530 - Isoparaffinic petroleum hydrocarbons, synthetic.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Isoparaffinic petroleum hydrocarbons, synthetic... hydrocarbons, synthetic. Isoparaffinic petroleum hydrocarbons, synthetic, may be safely used in the production... isoparaffinic petroleum hydrocarbons, produced by synthesis from petroleum gases consist of a mixture of...

  17. 40 CFR 92.119 - Hydrocarbon analyzer calibration.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 20 2014-07-01 2013-07-01 true Hydrocarbon analyzer calibration. 92... Hydrocarbon analyzer calibration. The HFID hydrocarbon analyzer shall receive the following initial and... into service and at least annually thereafter, the HFID hydrocarbon analyzer shall be adjusted...

  18. 40 CFR 86.1321-94 - Hydrocarbon analyzer calibration.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 20 2012-07-01 2012-07-01 false Hydrocarbon analyzer calibration. 86... Procedures § 86.1321-94 Hydrocarbon analyzer calibration. The FID hydrocarbon analyzer shall receive the... into service and at least annually thereafter, the FID hydrocarbon analyzer shall be adjusted...

  19. 21 CFR 178.3530 - Isoparaffinic petroleum hydrocarbons, synthetic.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Isoparaffinic petroleum hydrocarbons, synthetic... hydrocarbons, synthetic. Isoparaffinic petroleum hydrocarbons, synthetic, may be safely used in the production... isoparaffinic petroleum hydrocarbons, produced by synthesis from petroleum gases consist of a mixture of...

  20. 21 CFR 172.882 - Synthetic isoparaffinic petroleum hydrocarbons.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Synthetic isoparaffinic petroleum hydrocarbons... hydrocarbons. Synthetic isoparaffinic petroleum hydrocarbons may be safely used in food, in accordance with the... liquid hydrocarbons meeting the following specifications: Boiling point 93-260 °C as determined by...

  1. 40 CFR 92.119 - Hydrocarbon analyzer calibration.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 21 2013-07-01 2013-07-01 false Hydrocarbon analyzer calibration. 92... Hydrocarbon analyzer calibration. The HFID hydrocarbon analyzer shall receive the following initial and... into service and at least annually thereafter, the HFID hydrocarbon analyzer shall be adjusted...

  2. 40 CFR 86.1321-94 - Hydrocarbon analyzer calibration.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 19 2010-07-01 2010-07-01 false Hydrocarbon analyzer calibration. 86... Procedures § 86.1321-94 Hydrocarbon analyzer calibration. The FID hydrocarbon analyzer shall receive the... into service and at least annually thereafter, the FID hydrocarbon analyzer shall be adjusted...

  3. 21 CFR 172.882 - Synthetic isoparaffinic petroleum hydrocarbons.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Synthetic isoparaffinic petroleum hydrocarbons. 172... hydrocarbons. Synthetic isoparaffinic petroleum hydrocarbons may be safely used in food, in accordance with the... liquid hydrocarbons meeting the following specifications: Boiling point 93-260 °C as determined by...

  4. 21 CFR 178.3530 - Isoparaffinic petroleum hydrocarbons, synthetic.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Isoparaffinic petroleum hydrocarbons, synthetic... hydrocarbons, synthetic. Isoparaffinic petroleum hydrocarbons, synthetic, may be safely used in the production... isoparaffinic petroleum hydrocarbons, produced by synthesis from petroleum gases consist of a mixture of...

  5. 21 CFR 178.3530 - Isoparaffinic petroleum hydrocarbons, synthetic.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Isoparaffinic petroleum hydrocarbons, synthetic... hydrocarbons, synthetic. Isoparaffinic petroleum hydrocarbons, synthetic, may be safely used in the production... isoparaffinic petroleum hydrocarbons, produced by synthesis from petroleum gases consist of a mixture of...

  6. 21 CFR 172.882 - Synthetic isoparaffinic petroleum hydrocarbons.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Synthetic isoparaffinic petroleum hydrocarbons... hydrocarbons. Synthetic isoparaffinic petroleum hydrocarbons may be safely used in food, in accordance with the... liquid hydrocarbons meeting the following specifications: Boiling point 93-260 °C as determined by...

  7. 40 CFR 86.1321-94 - Hydrocarbon analyzer calibration.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 20 2013-07-01 2013-07-01 false Hydrocarbon analyzer calibration. 86... Procedures § 86.1321-94 Hydrocarbon analyzer calibration. The FID hydrocarbon analyzer shall receive the... into service and at least annually thereafter, the FID hydrocarbon analyzer shall be adjusted...

  8. 21 CFR 172.882 - Synthetic isoparaffinic petroleum hydrocarbons.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Synthetic isoparaffinic petroleum hydrocarbons... hydrocarbons. Synthetic isoparaffinic petroleum hydrocarbons may be safely used in food, in accordance with the... liquid hydrocarbons meeting the following specifications: Boiling point 93-260 °C as determined by...

  9. 40 CFR 92.119 - Hydrocarbon analyzer calibration.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 20 2011-07-01 2011-07-01 false Hydrocarbon analyzer calibration. 92... Hydrocarbon analyzer calibration. The HFID hydrocarbon analyzer shall receive the following initial and... into service and at least annually thereafter, the HFID hydrocarbon analyzer shall be adjusted...

  10. 40 CFR 86.317-79 - Hydrocarbon analyzer specifications.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 18 2010-07-01 2010-07-01 false Hydrocarbon analyzer specifications....317-79 Hydrocarbon analyzer specifications. (a) Hydrocarbon measurements are to be made with a heated... measures hydrocarbon emissions on a dry basis is permitted for gasoline-fueled testing; Provided,...

  11. 40 CFR 86.1321-94 - Hydrocarbon analyzer calibration.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 19 2011-07-01 2011-07-01 false Hydrocarbon analyzer calibration. 86... Procedures § 86.1321-94 Hydrocarbon analyzer calibration. The FID hydrocarbon analyzer shall receive the... into service and at least annually thereafter, the FID hydrocarbon analyzer shall be adjusted...

  12. 21 CFR 172.884 - Odorless light petroleum hydrocarbons.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Odorless light petroleum hydrocarbons. 172.884... § 172.884 Odorless light petroleum hydrocarbons. Odorless light petroleum hydrocarbons may be safely... liquid hydrocarbons derived from petroleum or synthesized from petroleum gases. The additive is...

  13. Selective photooxidation of hydrocarbons in zeolites by oxygen

    DOEpatents

    Frei, Heinz; Blatter, Fritz; Sun, Hai

    1998-01-01

    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.

  14. Geochemical methods of prospecting for hydrocarbons

    SciTech Connect

    Duchscherer, W. Jr.

    1980-12-01

    Because the commonly used reflection-seismograph exploration technique misses many marginal low-relief structural prospects and regardless of its electronic computer sophistication, overlooks almost all stratigraphic traps, the hydrocarbon exploration industry should take a look at geochemical prospecting methods, which detect geochemical anomalies in the near-surface soils by measuring the thermal dissociation of the soil carbonates that are found overlying hydrocarbon accumulations. To promote understanding of such prospecting techniques, Geochemical Surveys reviews the methods used, the soil-alteration patterns, the lateral and vertical migration of hydrocarbon gases, the halo phenomenon (a ring or annual anomaly), the geochemical modification of sediments, and the data-interpretation and exploration procedures involved in a carbonate ..delta.. C analysis, which measures the residual, stable, cumulative effect of hydrocarbon migration.

  15. METHODOLOGY FOR ESTIMATING NATURAL HYDROCARBON EMISSIONS

    EPA Science Inventory

    An emission inventory system for biogenic sources of hydrocarbons has been developed. It is based on modifications of the classic formula: Emissions = Sigma Biomass Area Emission Factor. It accommodates multiple sources with emission factors dependent on season, temperature and s...

  16. BIOREMEDIATED SOIL VENTING OF LIGHT HYDROCARBONS

    EPA Science Inventory

    The effectiveness and feasibility of bioremediated soil venting of light hydrocarbons in the unsaturated zone was investigated. Degradation mechanics were considered as a one dimensional balance of storage, linear sorption, vertical advection, and Michaelis-Menton kinetics. he re...

  17. Biodegradation of polycyclic hydrocarbons by Phanerochaete chrysosporium

    EPA Science Inventory

    The ability of the white rot fungus Phanerochaete chrysosporium to degrade polycyclic aromatic hydrocarbons (PAHs) that are present in anthracene oil (a distillation product obtained from coal tar) was demonstrated. Analysis by capillary gas chromatography and high-performance li...

  18. An Acid Hydrocarbon: A Chemical Paradox

    ERIC Educational Resources Information Center

    Burke, Jeffrey T.

    2004-01-01

    The chemical paradox of cyclopentadiene, a hydrocarbon, producing bubbles like a Bronsted acid is observed. The explanation that it is the comparative thermodynamic constancy of the fragrant cyclopentadienyl anion, which produces the powerful effect, resolves the paradox.

  19. Quantitative Hydrocarbon Energies from the PMO Method.

    ERIC Educational Resources Information Center

    Cooper, Charles F.

    1979-01-01

    Details a procedure for accurately calculating the quantum mechanical energies of hydrocarbons using the perturbational molecular orbital (PMO) method, which does not require the use of a computer. (BT)

  20. Method for determining permeability in hydrocarbon wells

    SciTech Connect

    Boone, D.E.

    1990-10-09

    This patent describes a method of determining at the earth's surface the permeability of a subsurface earth formation having a known nominal hydrocarbon pore saturation value. The formation is tranversed by a borehole resulting from drilling with a drill bit.

  1. MICROEMULSION FORMATION WITH MIXED CHLORINATED HYDROCARBON LIQUIDS

    EPA Science Inventory

    Mixing rules for water/chlorocarbon/anionic-surfactant systems have been studied. t was found that the behavior of chlorocarbons parallels the ideal mixing rules for hydrocarbons. he polarity of some chlorocarbons prevented a direct determination of electrolyte concentration and ...

  2. Silicon Carbide Transistor For Detecting Hydrocarbon Gases

    NASA Technical Reports Server (NTRS)

    Shields, Virgil B.; Ryan, Margaret A.; Williams, Roger M.

    1996-01-01

    Proposed silicon carbide variable-potential insulated-gate field-effect transistor specially designed for use in measuring concentrations of hydrocarbon gases. Devices like this prove useful numerous automotive, industrial, aeronautical, and environmental monitoring applications.

  3. Oxygenases for aliphatic hydrocarbons and fatty acids

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Oxygenases catalyzing the insertion of oxygen into either aliphatic hydrocarbons or fatty acids have great similarity. There are two classes of oxygenases: monooxygenases and dioxygenases. Dioxygenase inserts both atoms of molecular oxygen into a substrate, whereas monooxygenase incorporates one a...

  4. Hydrocarbon and nonhydrocarbon derivatives of cyclopropane

    NASA Technical Reports Server (NTRS)

    Slabey, Vernon A; Wise, Paul H; Gibbons, Louis C

    1953-01-01

    The methods used to prepare and purify 19 hydrocarbon derivatives of cyclopropane are discussed. Of these hydrocarbons, 13 were synthesized for the first time. In addition to the hydrocarbons, six cyclopropylcarbinols, five alkyl cyclopropyl ketones, three cyclopropyl chlorides, and one cyclopropanedicarboxylate were prepared as synthesis intermediates. The melting points, boiling points, refractive indices, densities, and, in some instances, heats of combustion of both the hydrocarbon and nonhydrocarbon derivatives of cyclopropane were determined. These data and the infrared spectrum of each of the 34 cyclopropane compounds are presented in this report. The infrared absorption bands characteristic of the cyclopropyl ring are discussed, and some observations are made on the contribution of the cyclopropyl ring to the molecular refractions of cyclopropane compounds.

  5. Deuterated polycyclic aromatic hydrocarbons: Revisited

    NASA Astrophysics Data System (ADS)

    Doney, K. D.; Candian, A.; Mori, T.; Onaka, T.; Tielens, A. G. G. M.

    2016-02-01

    Aims: The amount of deuterium locked up in polycyclic aromatic hydrocarbons (PAHs) has to date been an uncertain value. We present a near-infrared (NIR) spectroscopic survey of Hii regions in the Milky Way, Large Magellanic Cloud, and Small Magellanic Cloud obtained with AKARI, which aims to search for features indicative of deuterated PAHs (PAD or Dn-PAH) to better constrain the D/H ratio of PAHs. Methods: Fifty-three Hii regions were observed in the NIR (2.5-5 μm), using the Infrared Camera (IRC) on board the AKARI satellite. Through comparison of the observed spectra with a theoretical model of deuterated PAH vibrational modes, the aromatic and (a)symmetric aliphatic C-D stretch modes were identified. Results: We see emission features between 4.4-4.8 μm, which could be unambiguously attributed to deuterated PAHs in only six of the observed sources, all of which are located in the Milky Way. In all cases, the aromatic C-D stretching feature is weaker than the aliphatic C-D stretching feature, and, in the case of M17b, this feature is not observed at all. Based on the weak or absent PAD features in most of the observed spectra, it is suggested that the mechanism for PAH deuteration in the ISM is uncommon.

  6. Birds and polycyclic aromatic hydrocarbons

    USGS Publications Warehouse

    Albers, P.H.

    2006-01-01

    Polycyclic aromatic hydrocarbons (PAH) are present throughout the global environment and are produced naturally and by activities of humans. Effects of PAH on birds have been determined by studies employing egg injection, egg immersion, egg shell application, single and multiple oral doses, subcutaneous injection, and chemical analysis of field-collected eggs and tissue. The four-to six-ring aromatic compounds are the most toxic to embryos, young birds, and adult birds. For embryos, effects include death, developmental abnormalities, and a variety of cellular and biochemical responses. For adult and young birds, effects include reduced egg production and hatching, increased clutch or brood abandonment, reduced growth, increased organweights, and a variety of biochemical responses. Trophic level accumulation is unlikely. Environmental exposure to PAH in areas of high human population or habitats affected by recent petroleum spills might be sufficient to adversely affect reproduction. Evidence of long-term effects of elevated concentrations of environmental PAH on bird populations is very limited and the mechanisms of effect are unclear.

  7. The origin of light hydrocarbons

    SciTech Connect

    Mango, F.D.

    2000-04-01

    The light hydrocarbons (LHs) are probably intermediates in the catalytic decomposition of oil to gas. Two lines of evidence support this possibility. First, the reaction was duplicated experimentally under moderate conditions. Second, natural LHs exhibit the characteristics of catalytic products, in particular a proportionality between isomers: (xy{sub i})/(x{sub i}y) = {alpha} (where x and x{sub i} are isomers; y and y{sub i} are isomers that are structurally similar to x and x{sub i}; and {alpha} is a constant). All oils exhibit this relationship with coefficients of correlation reaching 0.99. Isomer ratios change systematically with concentrations, some approaching thermodynamic equilibrium, others not. The correlations reported are the strongest yet disclosed for the LHs. Isomers are related in triads (e.g., n-hexane {leftrightarrow} 2-methylpentane {leftrightarrow} 3-methylpentane), consistent with cyclopropane precursors. The LHs obtained experimentally are indistinguishable from natural LHs in (xy{sub i})/(x{sub i}y). These relationships are not explained by physical fractionations, equilibrium control, or noncatalytic modes of origin. A catalytic origin, on the other hand, has precedence, economy and experimental support.

  8. Total hydrocarbon analyzer evaluation study

    SciTech Connect

    Shamat, N. ); Crumpler, E. ); Roddan, A. )

    1991-10-01

    Measuring and controlling organic emissions from incineration processes has become a major environmental concern in recent years. The US Environmental Protection Agency (EPA) recently proposed a regulation for sewage sludge incinerators under section 405(d) of the Clean Water Act that will require all sludge incinerators to monitor total hydrocarbon emissions (THCs) on a continuous basis. Such a requirement would be part of National Pollutant Discharge Elimination (NPDES) permits and site-specific THC limits would be established for facilities based on a risk assessment of organic emissions. Before EPA can finalize the proposed requirement, THC monitoring must be successfully conducted in a plant environment and the system required by any final regulation must be kept in operation so that facilities can comply with their permits. The Metropolitan Waste Control Commission (MWCC) in St. Paul, Minn., and Rosemount Analytical Division in La Habre, Calif., entered into a joint agreement with EPA to demonstrate a hot' THC monitoring system to detect THCs in stack gases. The objectives of the study are to determine the feasibility of THC monitoring of sludge incinerator emissions; evaluate the long term reliability, cost of operation, and consistency of a continuous THC monitoring system in an incinerator environment; and determine the correlation of THC stack concentration to incinerator and scrubber operating conditions, carbon monoxide concentration, and specific VOC emissions.

  9. PROTONATED POLYCYCLIC AROMATIC HYDROCARBONS REVISITED

    SciTech Connect

    Ricca, Alessandra; Bauschlicher, Charles W. Jr; Allamandola, Louis J. E-mail: Charles.W.Bauschlicher@nasa.gov

    2011-02-01

    We reconsider the contribution that singly protonated polycyclic aromatic hydrocarbons (PAHs; HPAH{sup +}s) might make to the Class A component of the 6.2 {mu}m interstellar emission feature in light of the recent experimental measurements of protonated naphthalene and coronene. Our calculations on the small HPAH{sup +}s have a band near 6.2 {mu}m, as found in experiment. While the larger HPAH{sup +}s still have emission near 6.2 {mu}m, the much larger intensity of the band near 6.3 {mu}m overwhelms the weaker band at 6.2 {mu}m, so that the 6.2 {mu}m band is barely visible. Since the large PAHs are more representative of those in the interstellar medium, our work suggests that large HPAH{sup +}s cannot be major contributors to the observed emission at 6.2 {mu}m (i.e., Class A species). Saturating large PAH cations with hydrogen atoms retains the 6.2 {mu}m Class A band position, but the rest of the spectrum is inconsistent with observed spectra.

  10. Consider oxygen for hydrocarbon oxidations

    SciTech Connect

    Shahani, G.H.; Gunardson, H.H.; Easterbrook, N.C.

    1996-11-01

    A number of commodity petrochemicals are produced by the selective, catalytic oxidation of hydrocarbons in the liquid and gas phase. These chemicals are the basic building blocks for a host of chemical intermediates. Producing each of these chemicals requires large volumes of air or tonnage quantities of oxygen for oxidation. This oxidation can be carried out using air, oxygen-enriched air, or pure oxygen. Many oxidation processes, such as that for making ethylene oxide, originally were implemented using air but have switched to oxygen. Other processes, such as for vinyl acetate, were developed as oxygen-based processes directly. Over the years, using pure oxygen has become an accepted practice in a number of petrochemical processes, such as those for acetaldehyde, ethylene oxide, propylene oxide, vinyl acetate, and vinyl chloride. As the authors will discuss, using oxygen provides some significant advantages. So, the authors expect that the trend of existing air-based processes converting to oxygen will continue, while new processes based on oxygen will emerge.

  11. Steam Reforming of Hydrocarbon Fuels

    SciTech Connect

    Ming, Qimin; Healey, T; Allen, Lloyd; Irving, Patricia M.

    2002-12-01

    has developed a proprietary catalyst formulation for the fuel processor that is being developed for use with polymer electrolyte membrane fuel cells. The catalyst has been tested for the steam reforming of various hydrocarbons such as natural gas, iso-octane, retail gasoline, and hexadecane. A 300h continuous test has shown that the catalyst has very stable performance for steam reforming of iso-octane at 800?C with a steam/C ratio of 3.6. The same catalyst was also tested for steam reforming hexadecane (a surrogate of diesel) for 73h as well as natural gas for over 150h continuously, without deactivation or carbon deposition. Sulfur tolerance of the catalyst was tested using iso-octane containing various concentrations of sulfur. There was no catalyst deactivation after a 220h continuous test using iso-octane with 100ppm sulfur. For comparison, a nickel catalyst (12wt.% Ni/Al2O3) was also tested using different levels of sulfur in iso-octane. The results indicated that the InnovaTek catalyst has a substantially improved sulfur resistance compared to the nickel catalysts currently used for steam reforming. In addition, a variation of the catalyst was also used to reduce CO concentration to < 1% by water gas shift reaction.

  12. Hydrocarbon Biodegradation in Hypersaline Environments

    PubMed Central

    Ward, David M.; Brock, T. D.

    1978-01-01

    When mineral oil, hexadecane, and glutamate were added to natural samples of varying salinity (3.3 to 28.4%) from salt evaporation ponds and Great Salt Lake, Utah, rates of metabolism of these compounds decreased as salinity increased. Rate limitations did not appear to relate to low oxygen levels or to the availability of organic nutrients. Some oxidation of l-[U-14C]glutamic acid occurred even at extreme salinities, whereas oxidation of [1-14C]hexadecane was too low to be detected. Gas chromatographic examination of hexane-soluble components of tar samples from natural seeps at Rozel Point in Great Salt Lake demonstrated no evidence of biological oxidation of isoprenoid alkanes subject to degradation in normal environments. Some hexane-soluble components of the same tar were altered by incubation in a low-salinity enrichment culture inoculated with garden soil. Attempts to enrich for microorganisms in saline waters able to use mineral oil as a sole source of carbon and energy were successful below, but not above, about 20% salinity. This study strongly suggests a general reduction of metabolic rate at extreme salinities and raises doubt about the biodegradation of hydrocarbons in hypersaline environments. PMID:16345276

  13. Surface ionization of terpene hydrocarbons

    SciTech Connect

    Zandberg, E.Y.; Nezdyurov, A.L.; Paleev, V.I.; Ponomarev, D.A.

    1986-09-01

    By means of a surface ionization indicator for traces of materials in the atmosphere it has been established that many natural materials containing terpenes and their derivatives are ionized on the surface of heated molybdenum oxide at atmospheric air pressure. A mass-spectrometer method has been used to explain the mechanism of ionization of individual terpene hydrocarbons and to establish its principles. The ionization of ..cap alpha..-pinene, alloocimene, camphene, and also adamantane on oxidized tungsten under vacuum conditions has been investigated. The ..cap alpha..-pinene and alloocimene are ionized by surface ionization but camphene and adamantane are not ionized under vacuum conditions. The surface ionization mass spectra of ..cap alpha..-pinene and alloocimene are of low line brightness in comparison with electron ionization mass spectra and differ between themselves. The temperature relations for currents of the same compositions of ions during ionization of ..cap alpha..-pinene and alloocimene are also different, which leads to the possibility of surface ionization analysis of mixtures of terpenes being ionized. The ionization coefficients of alloocimene and ..cap alpha..-pinene on oxidized tungsten under temperatures optimum for ionization and the ionization potentials of alloocimene molecules and of radicals (M-H) of both compounds have been evaluated.

  14. Upgrading heavy hydrocarbon oils using sodium hypochlorite

    SciTech Connect

    Rankel, L.A.

    1986-07-22

    A process is described for demetallizing a residual hydrocarbon fraction comprising: (a) contacting the hydrocarbon fraction with an aqueous solution of a hypochlorite salt; (b) separating the mixture into an aqueous phase and an oil phase; (c) contacting the oil phase with a deasphalting solvent and (d) obtaining by separation a product comprising a demetallized oil fraction suitable for use as a feedstock for catalytic processing.

  15. Process for Photochemical Chlorination of Hydrocarbons

    DOEpatents

    Beanblossom, W S

    1951-08-28

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

  16. Antifoulant additive for light end hydrocarbons

    SciTech Connect

    Dickakian, G.B.

    1990-06-05

    This patent describes a method of treating a highly paraffinic hydrocarbon liquid containing not more than 5 wt% aromatics and from 10 to 10,000 ppm high molecular weight asphaltenes to prevent asphaltene fouling of equipment at temperatures below 400{degrees} F. It comprises: adding to the hydrocarbon liquid not less than 10 ppm and not more than 200 ppm of an oil soluble overbased magnesium alkyl aromatic sulfonate to inhibit asphaltene fouling.

  17. Formation of hydrocarbons by bacteria and algae

    SciTech Connect

    Tornabene, T.G.

    1980-12-01

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

  18. Hydrocarbon habitat of the west Netherlands basin

    SciTech Connect

    De Jager, J. ); Doyle, M. ); Grantham, P. ); Mabillard, J. )

    1993-09-01

    The complex West Netherlands Basin contains oil and gas in Triassic and Upper Jurassic to Cretaceous clastic reservoir sequences. The understanding has always been that the Carboniferous coal measures have generated only gas and the Jurassic marine Posidonia Shale only oil. However, detailed geochemical analyses show that both source rocks have generated oil and gas. Geochemical fingerprinting established a correlation of the hydrocarbons with the main source rocks. The occurrence of these different hydrocarbons is consistent with migration routes. Map-based charge modeling shows that the main phase of hydrocarbon generation occurred prior to the Late Cretaceous inversion of the West Netherlands Basin. However, along the southwest flank of the basin and in lows between the inversion highs, significant charge continued during the Tertiary. Biodegradation of oils in Jurassic and Cretaceous reservoirs occurred during the earliest Tertiary, but only in reservoirs that were at that time at temperatures of less then 70 to 80[degrees]C, where bacteria could survive. This study shows that also in a mature hydrocarbon province an integrated hydrocarbon habitat study with modern analyses and state-of-the-art technology can lead to a much improved understanding of the distribution of oil and gas in the subsurface. The results of this study will allow a better risk assessment for remaining prospects, and an improved prediction of the type of trapped hydrocarbons in terms of gas, oil, and biodegraded oil.

  19. Determination of the aromatic hydrocarbon to total hydrocarbon ratio of mineral oil in commercial lubricants.

    PubMed

    Uematsu, Yoko; Suzuki, Kumi; Ogimoto, Mami

    2016-03-01

    A method was developed to determine the aromatic hydrocarbon to total hydrocarbon ratio of mineral oil in commercial lubricants; a survey was also conducted of commercial lubricants. Hydrocarbons in lubricants were separated from the matrix components of lubricants using a silica gel solid phase extraction (SPE) column. Normal-phase liquid chromatography (NPLC) coupled with an evaporative light-scattering detector (ELSD) was used to determine the aromatic hydrocarbon to total hydrocarbon ratio. Size exclusion chromatography (SEC) coupled with a diode array detector (DAD) and a refractive index detector (RID) was used to estimate carbon numbers and the presence of aromatic hydrocarbons, which supplemented the results obtained by NPLC/ELSD. Aromatic hydrocarbons were not detected in 12 lubricants specified for use for incidental food contact, but were detected in 13 out of 22 lubricants non-specified for incidental food contact at a ratio up to 18%. They were also detected in 10 out of 12 lubricants collected at food factories at a ratio up to 13%. The centre carbon numbers of hydrocarbons in commercial lubricants were estimated to be between C16 and C50. PMID:26730677

  20. Hydrocarbon level detection with nanosecond laser ablation

    NASA Astrophysics Data System (ADS)

    Bidin, Noriah; Hosseinian S, Raheleh; Nugroho, Waskito; Mohd Marsin, Faridah; Zainal, Jasman

    2013-12-01

    Nanosecond laser induced breakdown in liquid is used as a technique to detect hydrocarbon levels in water. A Q-switched Nd:YAG laser was focused to generate optical breakdown associated with shock wave generation. The shock wave was propagated at the speed of sound in the medium after travelling 1 μs outward from the center of optical breakdown. Different amplitudes of sound were traced with the aid of an ultrasonic probe. The optical properties of the hydrocarbon solution were quantified via fundamental refractive index measurement (the Snell law). A continuous mode diode pumped solid state laser with second harmonic generation was used as the illumination light source. A CCD video camera with Matrox version 4.2 software was utilized to analyze the recording image. Option line analysis was performed to analyze the intensity of optical breakdown at different input energies. Gray level analysis was also conducted on the scattering light after passing through the hydrocarbon solution at different concentrations. The hydrocarbon solution comprised impurities or particles that varied according to the concentration. The average of the gray level is assumed to present the size of the particle. Inherently, as the acoustic wave propagates outward, it transports the mass (particles or impurities) and impacts on the ultrasonic probe. As a result a higher concentration of hydrocarbons reveals a larger amplitude of sound waves. This phenomenon is identified as a finger print for hydrocarbon levels between 100 and 1000 ppm. The transient detection, without complicated sampling preparation and no hazardous chemical involvement, makes laser ablation a promising technique to detect in situ hydrocarbon levels in water.

  1. Volatile hydrocarbons inhibit methanogenic crude oil degradation

    PubMed Central

    Sherry, Angela; Grant, Russell J.; Aitken, Carolyn M.; Jones, D. Martin; Head, Ian M.; Gray, Neil D.

    2014-01-01

    Methanogenic degradation of crude oil in subsurface sediments occurs slowly, but without the need for exogenous electron acceptors, is sustained for long periods and has enormous economic and environmental consequences. Here we show that volatile hydrocarbons are inhibitory to methanogenic oil biodegradation by comparing degradation of an artificially weathered crude oil with volatile hydrocarbons removed, with the same oil that was not weathered. Volatile hydrocarbons (nC5–nC10, methylcyclohexane, benzene, toluene, and xylenes) were quantified in the headspace of microcosms. Aliphatic (n-alkanes nC12–nC34) and aromatic hydrocarbons (4-methylbiphenyl, 3-methylbiphenyl, 2-methylnaphthalene, 1-methylnaphthalene) were quantified in the total hydrocarbon fraction extracted from the microcosms. 16S rRNA genes from key microorganisms known to play an important role in methanogenic alkane degradation (Smithella and Methanomicrobiales) were quantified by quantitative PCR. Methane production from degradation of weathered oil in microcosms was rapid (1.1 ± 0.1 μmol CH4/g sediment/day) with stoichiometric yields consistent with degradation of heavier n-alkanes (nC12–nC34). For non-weathered oil, degradation rates in microcosms were significantly lower (0.4 ± 0.3 μmol CH4/g sediment/day). This indicated that volatile hydrocarbons present in the non-weathered oil inhibit, but do not completely halt, methanogenic alkane biodegradation. These findings are significant with respect to rates of biodegradation of crude oils with abundant volatile hydrocarbons in anoxic, sulphate-depleted subsurface environments, such as contaminated marine sediments which have been entrained below the sulfate-reduction zone, as well as crude oil biodegradation in petroleum reservoirs and contaminated aquifers. PMID:24765087

  2. Hydrocarbons in soils: Origin, composition, and behavior (Review)

    NASA Astrophysics Data System (ADS)

    Gennadiev, A. N.; Pikovskii, Yu. I.; Tsibart, A. S.; Smirnova, M. A.

    2015-10-01

    It has been shown that a large body of evidence on the sources, transformation, and migration of hydrocarbons in soils has been acquired by different researchers. Available data about the origin and behavior of hydrocarbon gases, total petroleum hydrocarbons, polycyclic aromatic hydrocarbons, alkanes, and other compounds have been considered successively. A wide range of natural and anthropogenic factors affecting the transformation and migration of hydrocarbons in soils have been analyzed. The indicative value of these compounds has been explained. At the same time, many problems related to hydrocarbons in soils are still insufficiently understood. Sparse and fragmentary data are available in the literature on the interaction of different hydrocarbon groups in the soil. Few data refer to the features of hydrocarbons in background zonal soils; there are almost no interzonal comparisons. The behavior of hydrocarbons in soils of different landscape-geographical positions is characterized in isolated publications. The hydrocarbon status of soils as an integral complex of interrelated hydrocarbons is almost not analyzed. Hydrocarbons of a single class (polycyclic aromatic hydrocarbons, hydrocarbon gases, n-alkanes, etc.) are usually characterized in each publication.

  3. Chemical kinetic modeling of exhaust hydrocarbon oxidation

    SciTech Connect

    Wu, K.C.; Hochgreb, S.; Norris, M.B. . Dept. of Mechanical Engineering)

    1995-01-01

    Numerical simulations of the oxidation of unburned hydrocarbons from spark ignition engines were made based on full-chemistry, zero-dimensional models and compared with experiments for engine-out hydrocarbons and exhaust port oxidation. Simple correlations can be drawn between calculated results for hydrocarbon oxidation half-lives in plug or stirred reactors and measured hydrocarbon emissions. the extent of reaction through the exhaust port was simulated using calculated temperature histories for each burned gas mass element leaving the cylinder, coupled to detailed chemical kinetic rate equations. The results show that, for the fuels considered, the extent of oxidation of the remaining unburned fuel measured through the exhaust can be bracketed by the calculated results for the well-mixed (average) and core (adiabatically expanded) temperatures in the exhaust. Most of the oxidation is shown to occur at the very early exhaust times. For the paraffins considered, comparisons of simulations and experiments suggest that fuel oxidation is partially controlled by the mixing of cold gases at the initial stages of exhaust, where temperatures are high and the cold unburned mixture emerges from the wall layers into the exhaust jet. These conclusions are supported by the relatively small measured dependence on fuel type of the extent of oxidation in the exhaust, and by the resulting ratio of fuel to nonfuel hydrocarbons in the exhaust port exit.

  4. Thrust faulting and hydrocarbon generation: discussion

    SciTech Connect

    Warner, M.A.; Royse, F.

    1987-07-01

    Following the discovery of large volumes of hydrocarbons in the Cordilleran thrust belt of southwestern Wyoming and northern Utah, Angevine and Turcotte (1983), Edman and Surdam (1984), and Furlong and Edman (1984) discussed the role of thrust faulting in hydrocarbon generation. The authors concluded that overthrusting plays an important or even dominant role in the process of hydrocarbon generation in overthrust terrains. These conclusions may be in error because they are based on a mathematical analysis of thermal and geologic models that have little resemblance to actual thrust-belt geology. In this discussion, the authors discuss shortcomings of the thermal model used in the papers referred to above; emphasize the differences between their model and the geologic facts as they exist in thrust belts in general and in western Wyoming in particular; and caution readers about applying the conclusions based on such a model in the search for hydrocarbons. They contend that the temperature effects of thrust faulting were rather insignificant in the process of hydrocarbon generation in the Wyoming thrust belt.

  5. Foaming of mixtures of pure hydrocarbons

    NASA Technical Reports Server (NTRS)

    Robinson, J. V.; Woods, W. W.

    1950-01-01

    Mixtures of pure liquid hydrocarbons are capable of foaming. Nine hydrocarbons were mixed in pairs, in all possible combinations, and four proportions of each combination. These mixtures were sealed in glass tubes, and the foaming was tested by shaking. Mixtures of aliphatic with other aliphatic hydrocarbons, or of alkyl benzenes with other alkyl benzenes, did not foam. Mixtures of aliphatic hydrocarbons with alkyl benzenes did foam. The proportions of the mixtures greatly affected the foaming, the maximum foaming of 12 of 20 pairs being at the composition 20 percent aliphatic hydrocarbon, 80 percent alkyl benzene. Six seconds was the maximum foam lifetime of any of these mixtures. Aeroshell 120 lubricating oil was fractionated into 52 fractions and a residue by extraction with acetone in a fractionating extractor. The index of refraction, foam lifetime, color, and viscosity of these fractions were measured. Low viscosity and high index fractions were extracted first. The viscosity of the fractions extracted rose and the index decreased as fractionation proceeded. Foam lifetimes and color were lowest in the middle fractions. Significance is attached to the observation that none of the foam lifetimes of the fractions or residue is as high as the foam lifetime of the original Aeroshell, indicating that the foaming is not due to a particular foaming constituent, but rather to the entire mixture.

  6. Syngas Upgrading to Hydrocarbon Fuels Technology Pathway

    SciTech Connect

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

    2013-03-31

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

  7. Method for collecting and analyzing hydrocarbons

    SciTech Connect

    Ouellette, G.P.; Larter, S.R.; Fox, J.R.

    1988-12-20

    This patent describes a method for separating and collecting hydrocarbons which include methane from a gas obtained from the vicinity of an earth formation and obtaining information from such a gas which is useful in predicting the hydrocarbon potential of such an earth formation, the method comprising the steps of: obtaining a sample of a gas from the vicinity of an earth formation, the sample including methane; removing any water, carbon dioxide, and carbon monoxide from the sample and passing the sample through a cryogenic trap to separate and collect any interfering gases and hydrocarbons having at least two carbon atoms from the sample into the cryogenic trap. The removing and passing steps produce a first gas which contains the methane from the sample but which is free of water, carbon dioxide, carbon monoxide, interfering gases, and hydrocarbons having at least two carbon atoms; converting the methane in the first gas to form a condensed carbon dioxide sample; carrying out the removing, passing, and converting steps under a continuous subatmospheric pressure in such a manner as to prevent condensation of any oxygen in the cryogenic trap and to prevent any atmospheric carbon dioxide from entering into the sample, the first gas, the cryogenic trap, and the condensed carbon dioxide sample; determining the stable carbon isotope ratio of the condensed carbon dioxide sample which can be then be used to predict the hydrocarbon potential of the earth formation.

  8. Transpiration cooled throat for hydrocarbon rocket engines

    NASA Technical Reports Server (NTRS)

    May, Lee R.; Burkhardt, Wendel M.

    1991-01-01

    The objective for the Transpiration Cooled Throat for Hydrocarbon Rocket Engines Program was to characterize the use of hydrocarbon fuels as transpiration coolants for rocket nozzle throats. The hydrocarbon fuels investigated in this program were RP-1 and methane. To adequately characterize the above transpiration coolants, a program was planned which would (1) predict engine system performance and life enhancements due to transpiration cooling of the throat region using analytical models, anchored with available data; (2) a versatile transpiration cooled subscale rocket thrust chamber was designed and fabricated; (3) the subscale thrust chamber was tested over a limited range of conditions, e.g., coolant type, chamber pressure, transpiration cooled length, and coolant flow rate; and (4) detailed data analyses were conducted to determine the relationship between the key performance and life enhancement variables.

  9. Mechanisms of Hydrocarbon Based Polymer Etch

    NASA Astrophysics Data System (ADS)

    Lane, Barton; Ventzek, Peter; Matsukuma, Masaaki; Suzuki, Ayuta; Koshiishi, Akira

    2015-09-01

    Dry etch of hydrocarbon based polymers is important for semiconductor device manufacturing. The etch mechanisms for oxygen rich plasma etch of hydrocarbon based polymers has been studied but the mechanism for lean chemistries has received little attention. We report on an experimental and analytic study of the mechanism for etching of a hydrocarbon based polymer using an Ar/O2 chemistry in a single frequency 13.56 MHz test bed. The experimental study employs an analysis of transients from sequential oxidation and Ar sputtering steps using OES and surface analytics to constrain conceptual models for the etch mechanism. The conceptual model is consistent with observations from MD studies and surface analysis performed by Vegh et al. and Oehrlein et al. and other similar studies. Parameters of the model are fit using published data and the experimentally observed time scales.

  10. Using supercritical fluids to refine hydrocarbons

    DOEpatents

    Yarbro, Stephen Lee

    2014-11-25

    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.

  11. Methods for dispersing hydrocarbons using autoclaved bacteria

    DOEpatents

    Tyndall, Richard L.

    1996-01-01

    A method of dispersing a hydrocarbon includes the steps: providing a bacterium selected from the following group: ATCC 85527, ATCC 75529, and ATCC 55638, a mutant of any one of these bacteria possessing all the identifying characteristics of any one of these bacteria, and mixtures thereof; autoclaving the bacterium to derive a dispersant solution therefrom; and contacting the dispersant solution with a hydrocarbon to disperse the hydrocarbon. Moreover, a method for preparing a dispersant solution includes the following steps: providing a bacterium selected from the following group: ATCC 75527, ATCC 75529, and ATCC 55638, a mutant of any one of these bacteria possessing all the identifying characteristics of any one of these bacteria, and mixtures thereof; and autoclaving the bacterium to derive a dispersant solution therefrom.

  12. Methods for dispersing hydrocarbons using autoclaved bacteria

    DOEpatents

    Tyndall, R.L.

    1996-11-26

    A method of dispersing a hydrocarbon includes the following steps: providing a bacterium selected from the following group: ATCC 85527, ATCC 75529, and ATCC 55638, a mutant of any one of these bacteria possessing all the identifying characteristics of any one of these bacteria, and mixtures; autoclaving the bacterium to derive a dispersant solution; and contacting the dispersant solution with a hydrocarbon to disperse the hydrocarbon. Moreover, a method for preparing a dispersant solution includes the following steps: providing a bacterium selected from the following group: ATCC 75527, ATCC 75529, and ATCC 55638, a mutant of any one of these bacteria possessing all the identifying characteristics of any one of these bacteria, and mixtures; and autoclaving the bacterium to derive a dispersant solution.

  13. Bioremediation of Petroleum Hydrocarbon Contaminated Sites

    SciTech Connect

    Fallgren, Paul

    2009-03-30

    Bioremediation has been widely applied in the restoration of petroleum hydrocarbon-contaminated. Parameters that may affect the rate and efficiency of biodegradation include temperature, moisture, salinity, nutrient availability, microbial species, and type and concentration of contaminants. Other factors can also affect the success of the bioremediation treatment of contaminants, such as climatic conditions, soil type, soil permeability, contaminant distribution and concentration, and drainage. Western Research Institute in conjunction with TechLink Environmental, Inc. and the U.S. Department of Energy conducted laboratory studies to evaluate major parameters that contribute to the bioremediation of petroleum-contaminated drill cuttings using land farming and to develop a biotreatment cell to expedite biodegradation of hydrocarbons. Physical characteristics such as soil texture, hydraulic conductivity, and water retention were determined for the petroleum hydrocarbon contaminated soil. Soil texture was determined to be loamy sand to sand, and high hydraulic conductivity and low water retention was observed. Temperature appeared to have the greatest influence on biodegradation rates where high temperatures (>50 C) favored biodegradation. High nitrogen content in the form of ammonium enhanced biodegradation as well did the presence of water near field water holding capacity. Urea was not a good source of nitrogen and has detrimental effects for bioremediation for this site soil. Artificial sea water had little effect on biodegradation rates, but biodegradation rates decreased after increasing the concentrations of salts. Biotreatment cell (biocell) tests demonstrated hydrocarbon biodegradation can be enhanced substantially when utilizing a leachate recirculation design where a 72% reduction of hydrocarbon concentration was observed with a 72-h period at a treatment temperature of 50 C. Overall, this study demonstrates the investigation of the effects of

  14. Hydrocarbon plays evaluation of eastern China

    SciTech Connect

    Wu Shou Cheng )

    1991-03-01

    In eastern China there are 78 depressed basins, most of which are tilt-block basins. Each of them engenders petroleum generation except the Cretaceous sag basin of Song-Liao. These depressed basins set up in the order of older to younger depending on the change of the mantle convection. Consequently, the order of sedimentation and source-reservoir are changed and the exploration targets are also changed. Tan-Lu fault system is of great significance in NNW (early) and NEE (later) accompanying faults for exploration play. The hydrocarbon accumulation rules of these plays are: (1) As a result of the Tertiary tilt-block basins, compaction-flow basins contain similar hydrodynamic, thermodynamic, and buried pressure fields. The direction of fluid flow is from generation center of the basin to the margins. So the hydrocarbon plays are distributed nearby the generation center and circum-center belt. (2) The richness of hydrocarbon plays is controlled by the form and distribution of source rock due to structural change of the tilt-block. The richest is the center uplift play and then the low-raised play, steep slope play, gentle-slope play, and, poorest, the low-lying play. (3) A variety of the composite hydrocarbon play models are formed by the different structure models, sedimentary model, and hydrocarbon model. Most of the recovery reserves are set in one or two plays even though there are many hydrocarbon plays in a tilt-block basin. (4) There are 3 types and 25 subtypes of petroleum pools formed by the different characters of plays. Therefore, there are numerous technologies, methodologies, and strategies of petroleum exploration.

  15. Prediction of flame velocities of hydrocarbon flames

    NASA Technical Reports Server (NTRS)

    Dugger, Gordon L; Simon, Dorothy M

    1954-01-01

    The laminar-flame-velocity data previously reported by the Lewis Laboratory are surveyed with respect to the correspondence between experimental flame velocities and values predicted by semitheoretical and empirical methods. The combustible mixture variables covered are hydrocarbon structure (56 hydrocarbons), equivalence ratio of fuel-air mixture, mole fraction of oxygen in the primary oxygen-nitrogen mixture (0.17 to 0.50), and initial mixture temperature (200 degrees to 615 degrees k). The semitheoretical method of prediction considered are based on three approximate theoretical equations for flame velocity: the Semenov equation, the Tanford-Pease equation, and the Manson equation.

  16. Activation of hydrocarbons and the octane number

    NASA Technical Reports Server (NTRS)

    Peschard, Marcel

    1939-01-01

    This report presents an examination of the history of research on engine knocking and the various types of fuels used in the investigations of this phenomenon. According to this report, the spontaneous ignition of hydrocarbons doped with oxygen follows the logarithmic law within a certain temperature range, but not above 920 degrees K. Having extended the scope of investigations to prove hydrocarbons, the curves of the mixtures burned by air should then be established by progressive replacement of pure iso-octane with heptane. Pentane was also examined in this report.

  17. Aryl Hydrocarbon Receptor and Lung Cancer

    PubMed Central

    Tsay, Junchieh J.; Tchou-Wong, Kam-Meng; Greenberg, Alissa K.; Pass, Harvey; Rom, William N.

    2013-01-01

    The leading cause of lung cancer is exposure to cigarette smoke and other environmental pollutants, which include formaldehyde, acrolein, benzene, dioxin, and polycyclic aromatic hydrocarbons (PAHs). PAHs and dioxins are exogenous ligands that directly bind to the aryl hydrocarbon receptor (AhR), a transcription factor that activates xenobiotic metabolism, histone modification (an important step in DNA methylation), and, ultimately, tumorigenesis. Here we summarize the current understanding of AhR and its role in the development of lung cancer, including its influence on cell proliferation, angiogenesis, inflammation, and apoptosis. PMID:23564762

  18. Arabian plate hydrocarbon geology and potential

    SciTech Connect

    Beydoun, Z.R.

    1991-01-01

    This book provides a thought-provoking, succinct presentation of the geologic evolution and hydrocarbon potential of the world's most prolific petroleum province. The fascinating subjects discussed and documented include: What are the unique geologic factors that make the Middle East such a prolific province Where are the future Mesozoic and Tertiary plays What is the virtually untapped potential of the Paleozoic section What are the play potentials for underexplored areas such as Jordan, Syria, Yemen How are deeper drilling results shaping and modifying concepts of the Arabian plate history and pointing the way to future hydrocarbon targets

  19. Aliphatic hydrocarbons of the Murchison meteorite

    NASA Technical Reports Server (NTRS)

    Cronin, John R.; Pizzarello, Sandra

    1990-01-01

    Hydrocarbon fractions from the Murchison meteorite were prepared using benzene-methanol as the extraction solvent, fractionated on silica gel columns, and analyzed using gas chromatography combined with mass spectrometry and IR and NMR techniques. Results indicate that the most abundant aliphatic hydrocarbon components of the Murchison meteorite are C15 to C30 branched-alkyl-substituted mono-, di-, and tricyclic alkanes. It is shown that the n-alkanes, methyl alkanes, and isoprenoid alkanes that are sometimes found in extracts of the Murchison meteorite are terrestrial contaminants.

  20. [Storage of hydrocarbon-degrading bacteria].

    PubMed

    Bade, G M; Vecchioli, G I; del Panno, M T; Painceira, M T

    1994-01-01

    The storage in the laboratory of hydrocarbon degrading bacteria to be used in the decontamination of polluted sites or in the enhancement of biological treatment of industrial effluents was studied. Storage was carried out at 4 degrees C in nutrient agar and in a medium with selection pressure, liquid mineral medium with hydrocarbons. Storage at 4 degrees C with selection pressure and storage at -20 degrees C of 7 gram negative bacilli were compared. The former was the easiest method for preserving the greatest number of strains viable and active. PMID:7838975

  1. Detonability of hydrocarbon fuels in air

    NASA Technical Reports Server (NTRS)

    Beeson, H. D.; Mcclenagan, R. D.; Bishop, C. V.; Benz, F. J.; Pitz, W. J.; Westbrook, C. K.; Lee, J. H. S.

    1991-01-01

    Studies were conducted of the detonation of gas-phase mixtures of n-hexane and JP-4, with oxidizers as varied as air and pure oxygen, measuring detonation velocities and cell sizes as a function of stoichiometry and diluent concentration. The induction length of a one-dimensional Zeldovich-von Neumann-Doering detonation was calculated on the basis of a theoretical model that employed the reaction kinetics of the hydrocarbon fuels used. Critical energy and critical tube diameter are compared for a relative measure of the heavy hydrocarbon fuels studied; detonation sensitivity appears to increase slightly with increasing carbon number.

  2. Model advanced for hydrocarbon microseepage, related alterations

    SciTech Connect

    Thompson, C.K. ); Saunders, D.F.; Burson, K.R. )

    1994-11-14

    Future significant petroleum fields will be found in subtle stratigraphic traps in addition to structural traps. Both may be detectable by measuring surface hydrocarbon microseepage and related alterations. Reasons these methods have not been commonly used include: (1) early over-selling by some contractors with consequent bad client experiences, and (2) lack of generally accepted scientific models to relate anomalies to subsurface hydrocarbon accumulations. This article is restricted primarily to the authors' specific experience, studies, and conclusions over some 38 years with particular emphasis on the last 15 years. The authors believe these findings have resulted in improved wildcat success rates and realistic scientific models.

  3. Fire-eating: hazards of hydrocarbon aspiration.

    PubMed

    Guandalini, M; Steinke, K

    2007-12-01

    A 30-year-old male fire eater presented following aspiration of hydrocarbon fuel during a performance. A plain chest radiograph carried out 2 h after aspiration showed left lower lobe consolidation. The patient subsequently developed worsening shortness of breath, haemoptysis, fever and myalgia and a repeat plain chest radiograph showed extensive bilateral pulmonary consolidation with mediastinal and bilateral hilar lymphadenopathy. Computed tomography showed features consistent with necrotizing pneumonia. The clinical course was complicated by the development of large pleural effusions, pneumatocoeles and a spontaneous pneumothorax. Early abnormalities on a plain chest radiograph following suspected hydrocarbon aspiration require close monitoring for the development of further life-threatening complications. PMID:17958694

  4. Catalysts for synthesizing various short chain hydrocarbons

    DOEpatents

    Colmenares, Carlos

    1991-01-01

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

  5. Process for hydrogenation of hydrocarbon tars

    DOEpatents

    Dolbear, Geoffrey E.

    1978-07-18

    Hydrocarbon tars of high asphaltene content such as tars obtained from pyrolysis of coal are dissolved in a solvent formed from the hydrogenation of the coal tars, and the resultant mixture hydrogenated in the presence of a catalyst at a pressure from about 1500 to 5000 psig at a temperature from about 500.degree. F to about the critical temperature of the solvent to form a light hydrocarbon as a solvent for the tars. Hydrogen content is at least three times the amount of hydrogen consumed.

  6. Hydrocarbon disperse systems in electric fields

    SciTech Connect

    Deinega, Y.F.

    1983-07-01

    On the basis of method for regulating the smooth adjustment of the charge of the disperse phase of hydrocarbon systems in electric fields from positive to negative values by means of surfactants, a schematic electrokinetic picture of the behavior of the systems is derived. Changes in the structure of the disperse systems in electric fields have a substantial effect on the rheological properties of the system. The effect of electric fields on the formation of crystallization-condensation structures, the mechanism of electrical conduction with a high rate of deformation, and the many practical applications of electrical effects on hydrocarbon disperse systems are also studied.

  7. RADIO FREQUENCY ENHANCED DECONTAMINATION OF SOILS CONTAMINATED WITH HALOGENATED HYDROCARBONS

    EPA Science Inventory

    There has been considerable effort in the development of innovative treatment technologies for the clean up of sites containing hazardous wastes such as hydrocarbons and chlorinated hydrocarbons. Typical examples of such waste material are: chlorinated solvents, polychlorinated b...

  8. COMPOSITION OF AUTOMOBILE EVAPORATIVE AND TAILPIPE HYDROCARBON EMISSIONS

    EPA Science Inventory

    Mathematical modeling of ambient air photochemistry requires comprehensive mobile source hydrocarbon emissions speciation. Passenger car tailpipe and evaporative hydrocarbon emissions have been examined using procedures described in the Federal Register for emissions certificatio...

  9. BIOGENIC HYDROCARBONS IN THE ATMOSPHERIC BOUNDARY LAYER: A REVIEW

    EPA Science Inventory

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

  10. Effect of surface derived hydrocarbon impurities on Ar plasma properties

    SciTech Connect

    Fox-Lyon, Nick; Oehrlein, Gottlieb S.; Godyak, Valery

    2014-05-15

    The authors report on Langmuir probe measurements that show that hydrocarbon surfaces in contact with Ar plasma cause changes of electron energy distribution functions due to the flux of hydrogen and carbon atoms released by the surfaces. The authors compare the impact on plasma properties of hydrocarbon species gasified from an etching hydrocarbon surface with injection of gaseous hydrocarbons into Ar plasma. They find that both kinds of hydrocarbon injections decrease electron density and slightly increase electron temperatures of low pressure Ar plasma. For low percentages of impurities (∼1% impurity in Ar plasma explored here), surface-derived hydrocarbon species and gas phase injected hydrocarbon molecules cause similar changes of plasma properties for the same number of hydrocarbon molecules injected into Ar with a decrease in electron density of ∼4%.

  11. TRACE ANALYSIS FOR AROMATIC HYDROCARBONS IN NATURAL WATERS

    EPA Science Inventory

    A method of trace analysis of volatile aromatic hydrocarbons in natural water is described. The method is based on sparging water samples with nitrogen, adsorption of hydrocarbons on activated charcoal, followed by desorption into carbon disulfide and gas chromatographic analysis...

  12. THE UPTAKE OF AROMATIC AND BRANCHED CHAIN HYDROCARBONS BY YEAST

    EPA Science Inventory

    Studies of the hydrocarbon utilizing yeasts, Candida maltosa and C. lipolytica, have shown that both were capable of reducing recoverable amounts of branched chain and aromatic hydrocarbons in a mixture of naphthalene, tetradecane, hexadecane, pristane (tetra-methylpentadecane). ...

  13. Method and apparatus for low temperature destruction of halogenated hydrocarbons

    DOEpatents

    Reagen, William Kevin; Janikowski, Stuart Kevin

    1999-01-01

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

  14. Task 8: Evaluation of hydrocarbon potential

    SciTech Connect

    Cashman, P.H.; Trexler, J.H. Jr.

    1994-12-31

    Our studies focus on the stratigraphy of Late Devonian to early Pennsylvanian rocks at the NTS, because these are the best potential hydrocarbon source rocks in the vicinity of Yucca Mountain. In the last year, our stratigraphic studies have broadened to include the regional context for both the Chainman and the Eleana formations. New age data based on biostratigraphy constrain the age ranges of both Chainman and Eleana; accurate and reliable ages are essential for regional correlation and for regional paleogeographic reconstructions. Source rock analyses throughout the Chainman establish whether these rocks contained adequate organic material to generate hydrocarbons. Maturation analyses of samples from the Chainman determine whether the temperature history has been suitable for the generation of liquid hydrocarbons. Structural studies are aimed at defining the deformation histories and present position of the different packages of Devonian - Pennsylvanian rocks. This report summarizes new results of our structural, stratigraphic and hydrocarbon source rock potential studies at the Nevada Test Site and vicinity. Stratigraphy is considered first, with the Chainman Shale and Eleana Formation discussed separately. New biostratigraphic results are included in this section. New results from our structural studies are summarized next, followed by source rock and maturation analyses of the Chainman Shale. Directions for future work are included where appropriate.

  15. Site characterization and petroleum hydrocarbon plume mapping

    SciTech Connect

    Ravishankar, K.

    1996-12-31

    This paper presents a case study of site characterization and hydrocarbon contamination plume mapping/delineation in a gas processing plant in southern Mexico. The paper describes innovative and cost-effective use of passive (non-intrusive) and active (intrusive) techniques, including the use of compound-specific analytical methods for site characterization. The techniques used, on a demonstrative basis, include geophysical, geochemical, and borehole drilling. Geochemical techniques used to delineate the horizontal extent of hydrocarbon contamination at the site include soil gas surveys. The borehole drilling technique used to assess the vertical extent of contamination and confirm geophysical and geochemical data combines conventional hollow-stem auguring with direct push-probe using Geoprobe. Compound-specific analytical methods, such as hydrocarbon fingerprinting and a modified method for gasoline range organics, demonstrate the inherent merit and need for such analyses to properly characterize a site, while revealing the limitations of noncompound-specific total petroleum hydrocarbon analysis. The results indicate that the techniques used in tandem can properly delineate the nature and extent of contamination at a site; often supplement or complement data, while reducing the risk of errors and omissions during the assessment phase; and provide data constructively to focus site-specific remediation efforts. 7 figs.

  16. Volatile hydrocarbons and fuel oxygenates: Chapter 12

    USGS Publications Warehouse

    Cozzarelli, Isabelle M.

    2014-01-01

    Petroleum hydrocarbons and fuel oxygenates are among the most commonly occurring and widely distributed contaminants in the environment. This chapter presents a summary of the sources, transport, fate, and remediation of volatile fuel hydrocarbons and fuel additives in the environment. Much research has focused on the transport and transformation processes of petroleum hydrocarbons and fuel oxygenates, such as benzene, toluene, ethylbenzene, and xylenes and methyl tert‐butyl ether, in groundwater following release from underground storage tanks. Natural attenuation from biodegradation limits the movement of these contaminants and has received considerable attention as an environmental restoration option. This chapter summarizes approaches to environmental restoration, including those that rely on natural attenuation, and also engineered or enhanced remediation. Researchers are increasingly combining several microbial and molecular-based methods to give a complete picture of biodegradation potential and occurrence at contaminated field sites. New insights into the fate of petroleum hydrocarbons and fuel additives have been gained by recent advances in analytical tools and approaches, including stable isotope fractionation, analysis of metabolic intermediates, and direct microbial evidence. However, development of long-term detailed monitoring programs is required to further develop conceptual models of natural attenuation and increase our understanding of the behavior of contaminant mixtures in the subsurface.

  17. Advanced oxygen-hydrocarbon rocket engine study

    NASA Technical Reports Server (NTRS)

    Obrien, C. J.

    1980-01-01

    Preliminary identification and evaluation of promising liquid oxygen/ hydrocarbon (LO2/HC) rocket engine cycles is reported. A consistent and reliable data base for vehicle optimization and design studies, to demonstrate the significance of propulsion system improvements, and to select the critical technology areas necessary to realize such advances is presented.

  18. AMBIENT AIR NON-METHANE HYDROCARBON MONITOR

    EPA Science Inventory

    A monitor has been developed with adequate sensitivity and accuracy to measure continuously the concentration of non-methane hydrocarbons (NMHC) in ambient air. The monitor consists of pump and manifold system along with two basic instruments, a methane monitor and a flame-ioniza...

  19. SOURCE RECEPTOR METHODOLOGY FOR SOME CHLORINATED HYDROCARBONS

    EPA Science Inventory

    A source-receptor methodology is described that can be used to estimate emission rates of halogenated hydrocarbons from a manufacturing plant when access to the plant is not possible. An inert tracer is released at a known rate from a vehicle traveling back and forth on a road ou...

  20. Reduction of hydrocarbon emissions can be costly

    SciTech Connect

    Menke, T.R.

    1997-12-31

    The purpose of this paper is to share the Lone Star Greencastle Indiana Plant`s, experiences with changing raw materials in the kiln feed to reduce hydrocarbons emissions. The original change of the plant`s kiln feed composition was made in July of 1995. The plant changed the kiln feed composition for the first time since the plant opened. Shale was replaced in the kiln feed composition with clay, mill scale, and foundry sand, solely to reduce hydrocarbon emissions. At the time it was something that had to be done to keep burning liquid waste, in order to comply with the BIF Tier II limit of 20 ppm of hydrocarbon emissions. The change of raw materials did accomplish what it was supposed to by reducing the hydrocarbon emissions under the allowable limit. Plant personnel did not want to change raw materials, but did not have much of a choice, and had no idea of the repercussions that would follow. I will discuss the positives and negatives of the different raw mix compositions. 3 figs., 13 tabs.

  1. Measurement of hydrocarbon transport in bacteria

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Due to the hydrophobic, volatility, and relatively low aqueous solubility of aliphatic and aromatic hydrocarbons, transport of these chemicals by bacteria has not been extensively studied. These issues make transport assays difficult to carry out, and as a result, strong evidence for the active tran...

  2. Air Pollution: Where Do Hydrocarbons Come From?

    ERIC Educational Resources Information Center

    Maugh, Thomas H., II

    1975-01-01

    Describes the controversy surrounding a report which concluded that, in certain areas and under certain conditions, hydrocarbons released from trees and other vegetation may be more important in the initiation of smog than those released from automobiles. Discusses relevant research which has not been able to support or refute this conclusion.…

  3. Method of dispersing a hydrocarbon using bacteria

    DOEpatents

    Tyndall, R.L.

    1996-09-24

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

  4. Method of dispersing a hydrocarbon using bacteria

    DOEpatents

    Tyndall, Richard L.

    1996-01-01

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

  5. Natural hydrocarbons, urbanization, and urban ozone

    SciTech Connect

    Cardelino, C.A.; Chameides, W.L. )

    1990-08-20

    Using the Atlanta metropolitan area as a case study, the authors examine the effects of urbanization and its associated heat island on urban ozone concentrations. Air quality data from Atlanta suggest that urban ozone concentrations are enhanced by increases in ambient temperature. Model calculations suggest that this enhancement is caused by the effect of temperature on the atmospheric chemistry of peroxyacetyl nitrate (PAN), as well as the temperature dependence of natural and anthropogenic hydrocarbon emissions. A comparison of summertime temperatures in Atlanta and a nearby rural station, suggests that Atlanta's temperature over the past 15 years has increased by about 2{degree}C due to urbanization and its concomitant intensification of the urban heat island. Numerical simulations using conditions of a typical summertime day in Atlanta suggest that this rise in temperature could have, (1) resulted in a significant increase in the net emissions of natural hydrocarbons in the area in spite of the loss of about 20% of the areas forests over the same period, and (2) negated the beneficial effects on summertime ozone concentrations that would have been obtained from a 50% reduction in anthropogenic hydrocarbon emissions. Because a NO{sub x}-based ozone abatement strategy appears to be less sensitive to temperature increases than does a hydrocarbon-based strategy, a NO{sub x} strategy may prove to be more effective in the future if temperatures continue to rise as a result of urbanization and the greenhouse effect.

  6. Process for catalytic cracking of hydrocarbons

    SciTech Connect

    Goelzer, A.R.

    1991-04-23

    This patent describes improvement in a fluidized catalytic cracking-regeneration process for cracking hydrocarbon feedstocks or the vapors. The improvement consists of: cracking a first hydrocarbon feed comprising gas oil, residual oil boiling range material or mixtures thereof in a first elongated riser reactor in the presence of regenerated cracking catalyst supplied from the second catalyst regeneration zone at a temperature of at least 1300{degrees}F., cracking a second hydrocarbon feed comprising virgin naphtha, intermediate and heavy cracked naphtha boiling range material or mixtures thereof, having a boiling point to about 450{degrees}F., in a second elongated riser reactor in the presence of regenerated cracking catalyst supplied from the second catalyst regeneration zone at a temperature of at least 1300{degrees}F., combining the vaporous conversion products from the first and second elongated riser reactors in a common disengaging zone therein separating entrained catalyst particles from vaporous product material and passing the combined conversion products to a fractional distillation zone to recover at least a gasoline boiling range material fraction and lighter gaseous hydrocarbon material fraction, a light cycle oil boiling range material fraction and a heavy naphtha boiling range material fraction including slurry oil and higher boiling material fractions.

  7. Extracting hydrocarbons from water using a centrifuge

    NASA Astrophysics Data System (ADS)

    Ryabov, A. Yu.; Ilyina, A. A.; Chuikin, A. V.; Velikov, A. A.

    2014-09-01

    An original method for the solid-phase microextraction of hydrocarbons from water using a centrifuge is proposed. Comparative results from the chromatographic elution of substances after liquid-phase and solid-phase microextraction are presented. The percentage of the extraction of substances from aqueous solutions and the minimum detection limit for aromatic and aliphatic compounds are calculated.

  8. Apparatus for recovering gaseous hydrocarbons from hydrocarbon-containing solid hydrates

    DOEpatents

    Elliott, Guy R. B.; Barraclough, Bruce L.; Vanderborgh, Nicholas E.

    1984-01-01

    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.

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

    DOEpatents

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

    1981-02-19

    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.

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

    DOEpatents

    Elliott, Guy R. B.; Barraclough, Bruce L.; Vanderborgh, Nicholas E.

    1983-01-01

    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.

  11. Cuticular hydrocarbons from the bed bug Cimex lectularius L.

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Pentane extracts of male and female bed bugs were analyzed by gas chromatography and mass spectrometry in an effort to identify cuticular hydrocarbons. Seventeen hydrocarbons accounting for nearly 99% of the compounds eluting in the cuticular hydrocarbon region were identified. The sample contained ...

  12. Control and assessment of the hydrocarbon contamination of Ukrainian soils

    NASA Astrophysics Data System (ADS)

    Miroshnichenko, N. N.

    2008-05-01

    Regularities governing the self-purification of soils from oil hydrocarbons, as well as migration of hydrocarbons, and the effect on the water-physical properties and fertility of soils were revealed in a series of experiments. A system of ecological, economic, and reclamation standards was proposed for regulating economic activities in the case of soil contamination with hydrocarbons.

  13. Method for removing chlorine compounds from hydrocarbon mixtures

    DOEpatents

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

    1984-09-29

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

  14. Method for removing chlorine compounds from hydrocarbon mixtures

    DOEpatents

    Janoski, Edward J.; Hollstein, Elmer J.

    1985-12-31

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

  15. Assessment of undiscovered hydrocarbon resources of sub-Saharan Africa

    USGS Publications Warehouse

    Brownfield, Michael E.

    2016-01-01

    The assessment was geology-based and used the total petroleum system (TPS) concept. The geologic elements of a TPS are hydrocarbon source rocks (source rock maturation and hydrocarbon generation and migration), reservoir rocks (quality and distribution), and traps where hydrocarbon accumulates. Using these geologic criteria, 16 conventional total petroleum systems and 18 assessment units in the 13

  16. 40 CFR 721.10676 - Aromatic hydrocarbon mixture (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Aromatic hydrocarbon mixture (generic... Specific Chemical Substances § 721.10676 Aromatic hydrocarbon mixture (generic). (a) Chemical substance and... hydrocarbon mixture (PMN P-12-551) is subject to reporting under this section for the significant new...

  17. 40 CFR 86.1221-90 - Hydrocarbon analyzer calibration.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 19 2011-07-01 2011-07-01 false Hydrocarbon analyzer calibration. 86...-Fueled and Methanol-Fueled Heavy-Duty Vehicles § 86.1221-90 Hydrocarbon analyzer calibration. The FID hydrocarbon analyzer shall receive the following initial and periodic calibrations. (a) Initial and...

  18. 40 CFR 503.44 - Operational standard-total hydrocarbons.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... hydrocarbons. 503.44 Section 503.44 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... standard—total hydrocarbons. (a) The total hydrocarbons concentration in the exit gas from a sewage sludge incinerator shall be corrected for zero percent moisture by multiplying the measured total...

  19. 21 CFR 573.740 - Odorless light petroleum hydrocarbons.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 6 2013-04-01 2013-04-01 false Odorless light petroleum hydrocarbons. 573.740... ANIMALS Food Additive Listing § 573.740 Odorless light petroleum hydrocarbons. Odorless light petroleum hydrocarbons complying with § 172.884(a) and (b) of this chapter may be safely used in an amount not in...

  20. 40 CFR 721.4380 - Modified hydrocarbon resin.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Modified hydrocarbon resin. 721.4380... Substances § 721.4380 Modified hydrocarbon resin. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a modified hydrocarbon resin (P-91-1418)...

  1. 33 CFR 157.132 - Cargo tanks: Hydrocarbon vapor emissions.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 33 Navigation and Navigable Waters 2 2010-07-01 2010-07-01 false Cargo tanks: Hydrocarbon vapor... § 157.132 Cargo tanks: Hydrocarbon vapor emissions. Each tank vessel having a COW system under § 157.10a... must have— (a) A means to discharge hydrocarbon vapors from each cargo tank that is ballasted to...

  2. 40 CFR 721.10259 - Halogenated aromatic hydrocarbon (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Halogenated aromatic hydrocarbon... Specific Chemical Substances § 721.10259 Halogenated aromatic hydrocarbon (generic). (a) Chemical substance... halogenated aromatic hydrocarbon (PMN P-09-540) is subject to reporting under this section for the...

  3. 21 CFR 178.3650 - Odorless light petroleum hydrocarbons.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 21 Food and Drugs 3 2010-04-01 2009-04-01 true Odorless light petroleum hydrocarbons. 178.3650... SANITIZERS Certain Adjuvants and Production Aids § 178.3650 Odorless light petroleum hydrocarbons. Odorless light petroleum hydrocarbons may be safely used, as a component of nonfood articles intended for use...

  4. 33 CFR 157.132 - Cargo tanks: Hydrocarbon vapor emissions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 33 Navigation and Navigable Waters 2 2011-07-01 2011-07-01 false Cargo tanks: Hydrocarbon vapor... § 157.132 Cargo tanks: Hydrocarbon vapor emissions. Each tank vessel having a COW system under § 157.10a... must have— (a) A means to discharge hydrocarbon vapors from each cargo tank that is ballasted to...

  5. 40 CFR 52.987 - Control of hydrocarbon emissions.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 3 2012-07-01 2012-07-01 false Control of hydrocarbon emissions. 52... (CONTINUED) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Louisiana § 52.987 Control of hydrocarbon... compliance date of January 1, 1980. This shall result in an estimated hydrocarbon emission reduction of...

  6. 21 CFR 172.884 - Odorless light petroleum hydrocarbons.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Odorless light petroleum hydrocarbons. 172.884... HUMAN CONSUMPTION Multipurpose Additives § 172.884 Odorless light petroleum hydrocarbons. Odorless light petroleum hydrocarbons may be safely used in food, in accordance with the following prescribed...

  7. 40 CFR 86.1221-90 - Hydrocarbon analyzer calibration.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 20 2013-07-01 2013-07-01 false Hydrocarbon analyzer calibration. 86...-Fueled and Methanol-Fueled Heavy-Duty Vehicles § 86.1221-90 Hydrocarbon analyzer calibration. The FID hydrocarbon analyzer shall receive the following initial and periodic calibrations. (a) Initial and...

  8. 40 CFR 721.4365 - Substituted ethoxylated hydrocarbon (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Substituted ethoxylated hydrocarbon... Specific Chemical Substances § 721.4365 Substituted ethoxylated hydrocarbon (generic). (a) Chemical... as Substituted ethoxylated hydrocarbon (PMN P-99-0313) is subject to reporting under this section...

  9. 21 CFR 178.3650 - Odorless light petroleum hydrocarbons.

    Code of Federal Regulations, 2012 CFR

    2012-04-01

    ... 21 Food and Drugs 3 2012-04-01 2012-04-01 false Odorless light petroleum hydrocarbons. 178.3650... SANITIZERS Certain Adjuvants and Production Aids § 178.3650 Odorless light petroleum hydrocarbons. Odorless light petroleum hydrocarbons may be safely used, as a component of nonfood articles intended for use...

  10. 21 CFR 172.884 - Odorless light petroleum hydrocarbons.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 3 2011-04-01 2011-04-01 false Odorless light petroleum hydrocarbons. 172.884... HUMAN CONSUMPTION Multipurpose Additives § 172.884 Odorless light petroleum hydrocarbons. Odorless light petroleum hydrocarbons may be safely used in food, in accordance with the following prescribed...

  11. 40 CFR 721.4380 - Modified hydrocarbon resin.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Modified hydrocarbon resin. 721.4380... Substances § 721.4380 Modified hydrocarbon resin. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a modified hydrocarbon resin (P-91-1418)...

  12. 40 CFR 721.840 - Alkyl substituted diaromatic hydrocarbons.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... hydrocarbons. 721.840 Section 721.840 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.840 Alkyl substituted diaromatic hydrocarbons. (a) Chemical substance... alkyl substituted di-aro-matic hydrocarbons (PMN P-91-710) is subject to reporting under this...

  13. 40 CFR 503.44 - Operational standard-total hydrocarbons.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... hydrocarbons. 503.44 Section 503.44 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... standard—total hydrocarbons. (a) The total hydrocarbons concentration in the exit gas from a sewage sludge incinerator shall be corrected for zero percent moisture by multiplying the measured total...

  14. 40 CFR 721.840 - Alkyl substituted diaromatic hydrocarbons.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... hydrocarbons. 721.840 Section 721.840 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... Specific Chemical Substances § 721.840 Alkyl substituted diaromatic hydrocarbons. (a) Chemical substance... alkyl substituted di-aro-matic hydrocarbons (PMN P-91-710) is subject to reporting under this...

  15. 21 CFR 178.3530 - Isoparaffinic petroleum hydrocarbons, synthetic.

    Code of Federal Regulations, 2014 CFR

    2014-04-01

    ... 21 Food and Drugs 3 2014-04-01 2014-04-01 false Isoparaffinic petroleum hydrocarbons, synthetic... and Production Aids § 178.3530 Isoparaffinic petroleum hydrocarbons, synthetic. Isoparaffinic petroleum hydrocarbons, synthetic, may be safely used in the production of nonfood articles intended for...

  16. 40 CFR 721.10259 - Halogenated aromatic hydrocarbon (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Halogenated aromatic hydrocarbon... Specific Chemical Substances § 721.10259 Halogenated aromatic hydrocarbon (generic). (a) Chemical substance... halogenated aromatic hydrocarbon (PMN P-09-540) is subject to reporting under this section for the...

  17. 40 CFR 52.987 - Control of hydrocarbon emissions.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 3 2011-07-01 2011-07-01 false Control of hydrocarbon emissions. 52... (CONTINUED) APPROVAL AND PROMULGATION OF IMPLEMENTATION PLANS Louisiana § 52.987 Control of hydrocarbon... compliance date of January 1, 1980. This shall result in an estimated hydrocarbon emission reduction of...

  18. 21 CFR 178.3650 - Odorless light petroleum hydrocarbons.

    Code of Federal Regulations, 2013 CFR

    2013-04-01

    ... 21 Food and Drugs 3 2013-04-01 2013-04-01 false Odorless light petroleum hydrocarbons. 178.3650... SANITIZERS Certain Adjuvants and Production Aids § 178.3650 Odorless light petroleum hydrocarbons. Odorless light petroleum hydrocarbons may be safely used, as a component of nonfood articles intended for use...

  19. 40 CFR 86.331-79 - Hydrocarbon analyzer calibration.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 18 2010-07-01 2010-07-01 false Hydrocarbon analyzer calibration. 86....331-79 Hydrocarbon analyzer calibration. The following steps are followed in sequence to calibrate the hydrocarbon analyzer. It is suggested, but not required, that efforts be made to minimize relative...

  20. 27 CFR 21.125 - Rubber hydrocarbon solvent.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 27 Alcohol, Tobacco Products and Firearms 1 2010-04-01 2010-04-01 false Rubber hydrocarbon solvent. 21.125 Section 21.125 Alcohol, Tobacco Products and Firearms ALCOHOL AND TOBACCO TAX AND TRADE BUREAU....125 Rubber hydrocarbon solvent. (a) Rubber hydrocarbon solvent is a petroleum derivative....

  1. 21 CFR 573.740 - Odorless light petroleum hydrocarbons.

    Code of Federal Regulations, 2011 CFR

    2011-04-01

    ... 21 Food and Drugs 6 2011-04-01 2011-04-01 false Odorless light petroleum hydrocarbons. 573.740... ANIMALS Food Additive Listing § 573.740 Odorless light petroleum hydrocarbons. Odorless light petroleum hydrocarbons complying with § 172.884(a) and (b) of this chapter may be safely used in an amount not in...

  2. Method for recovering hydrocarbons from molten metal halides

    DOEpatents

    Pell, Melvyn B.

    1979-01-01

    In a process for hydrocracking heavy carbonaceous materials by contacting such carbonaceous materials with hydrogen in the presence of a molten metal halide catalyst to produce hydrocarbons having lower molecular weights and thereafter recovering the hydrocarbons so produced from the molten metal halide, an improvement comprising injecting into the spent molten metal halide, a liquid low-boiling hydrocarbon stream is disclosed.

  3. 33 CFR 157.132 - Cargo tanks: Hydrocarbon vapor emissions.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 33 Navigation and Navigable Waters 2 2013-07-01 2013-07-01 false Cargo tanks: Hydrocarbon vapor... § 157.132 Cargo tanks: Hydrocarbon vapor emissions. Each tank vessel having a COW system under § 157.10a... must have— (a) A means to discharge hydrocarbon vapors from each cargo tank that is ballasted to...

  4. 40 CFR 721.4365 - Substituted ethoxylated hydrocarbon (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Substituted ethoxylated hydrocarbon... Specific Chemical Substances § 721.4365 Substituted ethoxylated hydrocarbon (generic). (a) Chemical... as Substituted ethoxylated hydrocarbon (PMN P-99-0313) is subject to reporting under this section...

  5. 40 CFR 86.521-90 - Hydrocarbon analyzer calibration.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 19 2014-07-01 2014-07-01 false Hydrocarbon analyzer calibration. 86... Regulations for 1978 and Later New Motorcycles; Test Procedures § 86.521-90 Hydrocarbon analyzer calibration. (a) The FID hydrocarbon analyzer shall receive the following initial and periodic calibration....

  6. 40 CFR 721.10259 - Halogenated aromatic hydrocarbon (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Halogenated aromatic hydrocarbon... Specific Chemical Substances § 721.10259 Halogenated aromatic hydrocarbon (generic). (a) Chemical substance... halogenated aromatic hydrocarbon (PMN P-09-540) is subject to reporting under this section for the...

  7. 40 CFR 503.44 - Operational standard-total hydrocarbons.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... hydrocarbons. 503.44 Section 503.44 Protection of Environment ENVIRONMENTAL PROTECTION AGENCY (CONTINUED... standard—total hydrocarbons. (a) The total hydrocarbons concentration in the exit gas from a sewage sludge incinerator shall be corrected for zero percent moisture by multiplying the measured total...

  8. 40 CFR 721.10258 - Aromatic hydrocarbon (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Aromatic hydrocarbon (generic). 721... Substances § 721.10258 Aromatic hydrocarbon (generic). (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as aromatic hydrocarbon (PMN...

  9. 40 CFR 721.4380 - Modified hydrocarbon resin.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Modified hydrocarbon resin. 721.4380... Substances § 721.4380 Modified hydrocarbon resin. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified generically as a modified hydrocarbon resin (P-91-1418)...

  10. 40 CFR 86.331-79 - Hydrocarbon analyzer calibration.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 19 2012-07-01 2012-07-01 false Hydrocarbon analyzer calibration. 86....331-79 Hydrocarbon analyzer calibration. The following steps are followed in sequence to calibrate the hydrocarbon analyzer. It is suggested, but not required, that efforts be made to minimize relative...