Science.gov

Sample records for liquid hydrocarbons final

  1. Final report on APMP.M.FF-K2 bilateral comparison: Hydrocarbon liquid flow

    NASA Astrophysics Data System (ADS)

    Chen, I.-Cheng; Su, Chun-Min; Yang, Cheng-Tsair; Thai, Nguyen Hong

    2012-01-01

    This bilateral comparison was carried out in the field of liquid hydrocarbon flow following the Guidelines for CIPM Key Comparisons. This APMP.M.FF-K2 comparison involved two laboratories: Center for Measurement Standards (CMS, Chinese Taipei) and Vietnam Measurement Institute (VMI), which are both national standard calibration laboratories. The bilateral comparison was conducted using light liquid hydrocarbon across a flow range of 5 L s-1 to 30 L s-1. A Kral positive displacement meter served as the transfer standard. The Strouhal number and Reynolds number served as the key parameters for expressing the laboratories' measurements of volume and flowrate. The En value of the VMI test results with reference to CMS was 0.28. Main text. To reach the main text of this paper, click on Final Report. Note that this text is that which appears in Appendix B of the BIPM key comparison database kcdb.bipm.org/. The final report has been peer-reviewed and approved for publication by the CCM, according to the provisions of the CIPM Mutual Recognition Arrangement (CIPM MRA).

  2. Direct conversion of light hydrocarbon gases to liquid fuel. Final report No. 33

    SciTech Connect

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

    1992-05-16

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

  3. Conversion of associated natural gas to liquid hydrocarbons. Final report, June 1, 1995--January 31, 1997

    SciTech Connect

    1997-12-31

    The original concept envisioned for the use of Fischer-Tropsch processing (FTP) of United States associated natural gas in this study was to provide a way of utilizing gas which could not be brought to market because a pipeline was not available or for which there was no local use. Conversion of gas by FTP could provide a means of utilizing offshore associated gas which would not require installation of a pipeline or re-injection. The premium quality F-T hydrocarbons produced by conversion of the gas can be transported in the same way as the crude oil or in combination (blended) with it, eliminating the need for a separate gas transport system. FTP will produce a synthetic crude oil, thus increasing the effective size of the resource. The two conventional approaches currently used in US territory for handling of natural gas associated with crude petroleum production are re-injection and pipelining. Conversion of natural gas to a liquid product which can be transported to shore by tanker can be accomplished by FTP to produce hydrocarbons, or by conversion to chemical products such as methanol or ammonia, or by cryogenic liquefaction (LNG). This study considers FTP and briefly compares it to methanol and LNG. The Energy International Corporation cobalt catalyst, ratio adjusted, slurry bubble column F-T process was used as the basis for the study and the comparisons. An offshore F-T plant can best be accommodated by an FPSO (Floating Production, Storage, Offloading vessel) based on a converted surplus tanker, such as have been frequently used around the world recently. Other structure types used in deep water (platforms) are more expensive and cannot handle the required load.

  4. Hydropyrolysis of biomass to produce liquid hydrocarbon fuels. Final report. Biomass Alternative-Fuels Program

    SciTech Connect

    Fujita, R K; Bodle, W W; Yuen, P C

    1982-10-01

    The ojective of the study is to provide a process design and cost estimates for a biomass hydropyrolysis plant and to establish its economic viability for commercial applications. A plant site, size, product slate, and the most probable feedstock or combination of feedstocks were determined. A base case design was made by adapting IGT's HYFLEX process to Hawaiian biomass feedstocks. The HYFLEX process was developed by IGT to produce liquid and/or gaseous fuels from carbonaceous materials. The essence of the process is the simultaneous extraction of valuable oil and gaseous products from cellulosic biomass feedstocks without forming a heavy hard-to-handle tar. By controlling rection time and temperature, the product slate can be varied according to feedstock and market demand. An optimum design and a final assessment of the applicability of the HYFLEX process to the conversion of Hawaiian biomass was made. In order to determine what feedstocks could be available in Hawaii to meet the demands of the proposed hydropyrolysis plant, various biomass sources were studied. These included sugarcane and pineapple wastes, indigenous and cultivated trees and indigenous and cultivated shrubs and grasses.

  5. Enhanced liquid hydrocarbon recovery process

    SciTech Connect

    Sydansk, R.D.

    1992-07-14

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

  6. LIQUID HYDROCARBON FUEL CELL DEVELOPMENT.

    DTIC Science & Technology

    A compound anode consists of a reforming catalyst bed in direct contact with a palladium-silver fuel cell anode. The objective of this study was to...prove the feasibility of operating a compound anode fuel cell on a liquid hydrocarbon and to define the important parameters that influence cell...performance. Both reformer and fuel cell tests were conducted with various liquid hydrocarbon fuels. Included in this report is a description of the

  7. Final report on the key comparison of hydrocarbon liquid flow: CCM.FF-K2.2015

    NASA Astrophysics Data System (ADS)

    Shimada, T.; Bittner-Rohrhofer, K.; Medina López, V. J.; Arias, R.; Su, C.-M.; Chen, I.-C.; Ribere, F.; Rowan, L.; Dignan, S.

    2016-01-01

    Seven laboratories: BEV (Austria), CENAM (Mexico), CMS (Chinese-Taipei), LNE-TRAPIL (France), NEL (United Kingdom), NMIA (Australia), and the pilot lab NMIJ (Japan), participated in the key comparison CCM.FF-K2.2015 for hydrocarbon flow measurement. A screw type positive displacement flow meter was selected as a transfer standard. The calibration stability of the transfer standard was evaluated from repeated measurements by NMIJ and showed standard reproducibility of 0.0035 %. The transfer standard was also thoroughly tested for sensitivity to temperature, viscosity, pressure, and other effects. The uncertainty due to the transfer standard of 0.0080 % was less than the quoted uncertainties of the participants. The key comparison reference values (KCRVs) at Reynolds number of 70 000 and 300 000 were obtained as the weighted mean from the calibration results, and the KCRV at Reynolds number of 100 000 was obtained as the median by using the Monte Carlo method according to Cox's procedure B, since the consistency check at Reynolds number of 100 000 failed at the 95 % confidence level. All participant results selected to determine the KCRVs have En values which show consistency with the evaluated KCRVs. Main text To reach the main text of this paper, click on Final Report. Note that this text is that which appears in Appendix B of the BIPM key comparison database kcdb.bipm.org/. The final report has been peer-reviewed and approved for publication by the CCM, according to the provisions of the CIPM Mutual Recognition Arrangement (CIPM MRA).

  8. Final report on the APMP key comparison liquid hydrocarbon flow (APMP.M.FF-K2.a)

    NASA Astrophysics Data System (ADS)

    Shimada, Takashi; Su, Chun-Min; Chen, I.-Cheng; Dignan, Simon

    2017-01-01

    A key comparison, APMP.M.FF-K2. was undertaken by the APMP Technical Committee for Fluid Flow, and was piloted by the National Metrology Institute of Japan (NMIJ/AIST). The objective of this key comparison is to demonstrate the degree of equivalence of the hydrocarbon flow standards held at the participating laboratories (CMS, NMIA and NMIJ), to link the key comparison reference value (KCRV) of CCM.FF-K2 and to provide supporting evidence for the calibration and measurement capabilities (CMCs) claimed by the participating laboratories in the Asia-Pacific regions. A screw type positive displacement flow meter was selected as a transfer standard. The performance of the transfer standard and its stability was evaluated from repeated measurements by the pilot institute, NMIJ. The transfer standard showed high performance and good stability since the uncertainty due to the transfer standard was less than quoted uncertainties in the participants. CMS and NMIJ have En values which show consistency with both the relevant KCRV for APMP.M.FF-K2.a and each pair of participants. However some En values for NMIA were from 1 to 1.2, indicating 'alert'. Main text To reach the main text of this paper, click on Final Report. Note that this text is that which appears in Appendix B of the BIPM key comparison database kcdb.bipm.org/. The final report has been peer-reviewed and approved for publication by the CCM, according to the provisions of the CIPM Mutual Recognition Arrangement (CIPM MRA).

  9. Process for vaporizing a liquid hydrocarbon fuel

    DOEpatents

    Szydlowski, Donald F.; Kuzminskas, Vaidotas; Bittner, Joseph E.

    1981-01-01

    The object of the invention is to provide a process for vaporizing liquid hydrocarbon fuels efficiently and without the formation of carbon residue on the apparatus used. The process includes simultaneously passing the liquid fuel and an inert hot gas downwardly through a plurality of vertically spaed apart regions of high surface area packing material. The liquid thinly coats the packing surface, and the sensible heat of the hot gas vaporizes this coating of liquid. Unvaporized liquid passing through one region of packing is uniformly redistributed over the top surface of the next region until all fuel has been vaporized using only the sensible heat of the hot gas stream.

  10. Microwave plasma in hydrocarbon liquids

    NASA Astrophysics Data System (ADS)

    Nomura, Shinfuku; Toyota, Hiromichi; Mukasa, Shinobu; Yamashita, Hiroshi; Maehara, Tsunehiro; Kuramoto, Makoto

    2006-05-01

    The generation of microwave plasma in liquid with vapor bubbles has been achieved and will soon be applied to high-speed chemical vapor deposition. Vapor bubbles are induced from an electrode by heating. The deposition rate of diamondlike carbon films depends on the pressure and the power of the microwave supply. Polycrystalline silicon carbide is synthesized on a silicon substrate in a mixture of n-dodecane and silicone oil. The dispersion of water droplets in liquid creates many pores on the silicon carbide films. The synthesis of carbon nanotubes can be achieved in liquid benzene.

  11. 30 CFR 250.1202 - Liquid hydrocarbon measurement.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 30 Mineral Resources 2 2014-07-01 2014-07-01 false Liquid hydrocarbon measurement. 250.1202... Measurement, Surface Commingling, and Security § 250.1202 Liquid hydrocarbon measurement. (a) What are the requirements for measuring liquid hydrocarbons? You must: (1) Submit a written application to, and obtain...

  12. 30 CFR 250.1202 - Liquid hydrocarbon measurement.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 30 Mineral Resources 2 2012-07-01 2012-07-01 false Liquid hydrocarbon measurement. 250.1202... Measurement, Surface Commingling, and Security § 250.1202 Liquid hydrocarbon measurement. (a) What are the requirements for measuring liquid hydrocarbons? You must: (1) Submit a written application to, and obtain...

  13. 30 CFR 250.1202 - Liquid hydrocarbon measurement.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 30 Mineral Resources 2 2013-07-01 2013-07-01 false Liquid hydrocarbon measurement. 250.1202... Measurement, Surface Commingling, and Security § 250.1202 Liquid hydrocarbon measurement. (a) What are the requirements for measuring liquid hydrocarbons? You must: (1) Submit a written application to, and obtain...

  14. 30 CFR 250.1202 - Liquid hydrocarbon measurement.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 30 Mineral Resources 2 2010-07-01 2010-07-01 false Liquid hydrocarbon measurement. 250.1202..., Surface Commingling, and Security § 250.1202 Liquid hydrocarbon measurement. (a) What are the requirements for measuring liquid hydrocarbons? You must: (1) Submit a written application to, and obtain approval...

  15. 30 CFR 250.1202 - Liquid hydrocarbon measurement.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 30 Mineral Resources 2 2011-07-01 2011-07-01 false Liquid hydrocarbon measurement. 250.1202... Gas Production Measurement, Surface Commingling, and Security § 250.1202 Liquid hydrocarbon measurement. (a) What are the requirements for measuring liquid hydrocarbons? You must: (1) Submit a written...

  16. Process for the production of liquid hydrocarbons

    DOEpatents

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

    2006-06-27

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

  17. Evaporation of Liquid Hydrocarbon Mixtures on Titan

    NASA Astrophysics Data System (ADS)

    Luspay-Kuti, Adrienn; Chevrier, V. F.; Rivera-Valentin, E. G.; Singh, S.; Roe, L. A.; Wagner, A.

    2013-10-01

    Besides Earth, Titan is the only other known planetary body with proven stable liquids on its surface. The hydrological cycle of these liquid hydrocarbon mixtures is critical in understanding Titan’s atmosphere and surface features. Evaporation of liquid surface bodies has been indirectly observed as shoreline changes from measurements by Cassini ISS and RADAR (Hayes et al. 2011, Icarus 211, 655-671; Turtle et al. 2011, Science 18, 1414-1417.), but the long seasons of Saturn strongly limit the time span of these observations and their validity over the course of an entire Titan year. Using a novel Titan simulation chamber, the evaporation rate of liquid methane and dissolved nitrogen mixture under Titan surface conditions was derived (Luspay-Kuti et al. 2012, GRL 39, L23203), which is especially applicable to low latitude transient liquids. Polar lakes, though, are expected to be composed of a variety of hydrocarbons, primarily a mixture of ethane and methane (e.g. Cordier et al. 2009, ApJL 707, L128-L131). Here we performed laboratory simulations of ethane-methane mixtures with varying mole fraction under conditions suitable for the polar regions of Titan. We will discuss results specifically addressing the evaporation behavior as the solution becomes increasingly ethane dominated, providing quantitative values for the evaporation rate at every step. These laboratory results are relevant to polar lakes, such as Ontario Lacus, and can shed light on their stability.

  18. Assessment of plant-derived hydrocarbons. Final report

    SciTech Connect

    McFadden, K.; Nelson, S.H.

    1981-09-30

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

  19. Formulating liquid hydrocarbon fuels for SOFCs

    NASA Astrophysics Data System (ADS)

    Saunders, G. J.; Preece, J.; Kendall, K.

    The injection of liquid hydrocarbons directly into an SOFC system is considered for application to hybrid vehicles. The main problem is carbon deposition on the nickel anode when molecules such as ethanol or iso-octane are injected directly. Such carbon deposition has been studied using a microtubular SOFC with a mass spectrometer analysing the product gases to investigate the reaction sequence and also to investigate the deposited carbon by temperature programmed oxidation (TPO). The results show that only two liquids could be injected directly onto nickel cermet anodes without serious carbon blockage, methanol and methanoic acid. Even then, TPO experiments revealed deposition of small amounts of carbon which could be prevented by small additions of air or water to the fuel. Gasoline type molecules like iso-octane killed the SOFC in about 30 min operation, with about 90% of the molecular carbon being deposited on the nickel cermet anode. However, certain mixtures of iso-octane, water, alcohol and surfactant were found to produce beneficial results with remarkably low carbon deposition, less than 1% of the molecular carbon appearing on the anode. Such formulations had octane numbers appropriate to internal combustion engine operation.

  20. Catalysts for converting syngas into liquid hydrocarbons and methods thereof

    DOEpatents

    Yu, Fei; Yan, Qiangu; Batchelor, William

    2016-03-15

    The presently-disclosed subject matter includes methods for producing liquid hydrocarbons from syngas. In some embodiments the syngas is obtained from biomass and/or comprises a relatively high amount of nitrogen and/or carbon dioxide. In some embodiments the present methods can convert syngas into liquid hydrocarbons through a one-stage process. Also provided are catalysts for producing liquid hydrocarbons from syngas, wherein the catalysts include a base material, a transition metal, and a promoter. In some embodiments the base material includes a zeolite-iron material or a cobalt-molybdenum carbide material. In still further embodiments the promoter can include an alkali metal.

  1. Hydrocarbon content of geopressured brines. Final report

    SciTech Connect

    Osif, T.L.

    1985-08-01

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

  2. Using Ionic Liquids in Selective Hydrocarbon Conversion Processes

    SciTech Connect

    Tang, Yongchun; Periana, Roy; Chen, Weiqun; van Duin, Adri; Nielsen, Robert; Shuler, Patrick; Ma, Qisheng; Blanco, Mario; Li, Zaiwei; Oxgaard, Jonas; Cheng, Jihong; Cheung, Sam; Pudar, Sanja

    2009-09-28

    This is the Final Report of the five-year project Using Ionic Liquids in Selective Hydrocarbon Conversion Processes (DE-FC36-04GO14276, July 1, 2004- June 30, 2009), in which we present our major accomplishments with detailed descriptions of our experimental and theoretical efforts. Upon the successful conduction of this project, we have followed our proposed breakdown work structure completing most of the technical tasks. Finally, we have developed and demonstrated several optimized homogenously catalytic methane conversion systems involving applications of novel ionic liquids, which present much more superior performance than the Catalytica system (the best-to-date system) in terms of three times higher reaction rates and longer catalysts lifetime and much stronger resistance to water deactivation. We have developed in-depth mechanistic understandings on the complicated chemistry involved in homogenously catalytic methane oxidation as well as developed the unique yet effective experimental protocols (reactors, analytical tools and screening methodologies) for achieving a highly efficient yet economically feasible and environmentally friendly catalytic methane conversion system. The most important findings have been published, patented as well as reported to DOE in this Final Report and our 20 Quarterly Reports.

  3. Liquid hydrocarbons probable under Ross Sea

    USGS Publications Warehouse

    Cooper, A. K.; Davey, F.J.; Hinz, K.

    1988-01-01

    Thick glacial strata, which have no source-rock potential, cover the Ross Sea. If these strata persist to great depths, then hydrocarbon-generation prospects will be poor. Deeply buried strata within Ross Sea rift-grabens, if like other Gondwana rift-deposits, could have good potential for hydrocarbon generation. Current hydrocarbon assessments of the Ross Sea and adjacent areas must be considered highly speculative because the deeply buried rift(?) strata have not been sampled in situ. The assessment of the Ross Sea relies on geophysical/geologic data, two-stage rift models, and data from formerly nearby Gondwana rift-basins. We conclude that conditions favorable for hydrocarbon generation and entrapment are likely throughout the Ross Sea, and especially in the Victoria Land basin, if adequate source beds exist. -Authors

  4. Cooling and solidification of heavy hydrocarbon liquid streams

    DOEpatents

    Antieri, Salvatore J.; Comolli, Alfred G.

    1983-01-01

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

  5. Direct conversion of light hydrocarbon gases to liquid fuel

    SciTech Connect

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

    1992-05-16

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

  6. Liquid fuels production from biomass. Final report

    SciTech Connect

    Levy, P. F.; Sanderson, J. E.; Ashare, E.; Wise, D. L.; Molyneaux, M. S.

    1980-06-30

    The current program to convert biomass into liquid hydrocarbon fuels is an extension of a previous program to ferment marine algae to acetic acid. In that study it was found that marine algae could be converted to higher aliphatic organic acids and that these acids could be readily removed from the fermentation broth by membrane or liquid-liquid extraction. It was then proposed to convert these higher organic acids via Kolbe electrolysis to aliphatic hydrocarbons, which may be used as a diesel fuel. The specific goals for the current porgram are: (1) establish conditions under which substrates other than marine algae may be converted in good yield to organic acids, here the primary task is methane suppression; (2) modify the current 300-liter fixed packed bed batch fermenter to operate in a continuous mode; (3) change from membrane extraction of organic acids to liquid-liquid extraction; (4) optimize the energy balance of the electrolytic oxidation process, the primary task is to reduce the working potential required for the electrolysis while maintaining an adequate current density; (5) scale the entire process up to match the output of the 300 liter fermenter; and (6) design pilot plant and commercial size plant (1000 tons/day) processes for converting biomass to liquid hydrocarbon fuels and perform an economic analysis for the 1000 ton/day design.

  7. 30 CFR 250.1162 - When may I burn produced liquid hydrocarbons?

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 30 Mineral Resources 2 2013-07-01 2013-07-01 false When may I burn produced liquid hydrocarbons... Gas Production Requirements Flaring, Venting, and Burning Hydrocarbons § 250.1162 When may I burn... burn any produced liquid hydrocarbons. The Regional Supervisor may allow you to burn liquid...

  8. 30 CFR 250.1162 - When may I burn produced liquid hydrocarbons?

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 30 Mineral Resources 2 2010-07-01 2010-07-01 false When may I burn produced liquid hydrocarbons... Requirements Flaring, Venting, and Burning Hydrocarbons § 250.1162 When may I burn produced liquid hydrocarbons? (a) You must request and receive approval from the Regional Supervisor to burn any produced liquid...

  9. 30 CFR 250.1162 - When may I burn produced liquid hydrocarbons?

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 30 Mineral Resources 2 2014-07-01 2014-07-01 false When may I burn produced liquid hydrocarbons... Gas Production Requirements Flaring, Venting, and Burning Hydrocarbons § 250.1162 When may I burn... burn any produced liquid hydrocarbons. The Regional Supervisor may allow you to burn liquid...

  10. 30 CFR 250.1162 - When may I burn produced liquid hydrocarbons?

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 30 Mineral Resources 2 2012-07-01 2012-07-01 false When may I burn produced liquid hydrocarbons... Gas Production Requirements Flaring, Venting, and Burning Hydrocarbons § 250.1162 When may I burn... burn any produced liquid hydrocarbons. The Regional Supervisor may allow you to burn liquid...

  11. Process of producing liquid hydrocarbon fuels from biomass

    DOEpatents

    Kuester, James L.

    1987-07-07

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

  12. Process of producing liquid hydrocarbon fuels from biomass

    DOEpatents

    Kuester, J.L.

    1987-07-07

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

  13. Liquid-liquid equilibria of binary mixtures of a lipidic ionic liquid with hydrocarbons.

    PubMed

    Green, Blane D; Badini, Alexander J; O'Brien, Richard A; Davis, James H; West, Kevin N

    2016-01-28

    Although structurally diverse, many ionic liquids (ILs) are polar in nature due to the strong coulombic forces inherent in ionic compounds. However, the overall polarity of the IL can be tuned by incorporating significant nonpolar content into one or more of the constituent ions. In this work, the binary liquid-liquid equilibria of one such IL, 1-methyl-3-(Z-octadec-9-enyl)imidazolium bistriflimide, with several hydrocarbons (n-hexane, n-octane, n-decane, cyclohexane, methylcyclohexane, 1-octene) is measured over the temperature range 0-70 °C at ambient pressure using a combination of cloud point and gravimetric techniques. The phase behavior of the systems are similar in that they exhibit two phases: one that is 60-90 mole% hydrocarbon and a second phase that is nearly pure hydrocarbon. Each phase exhibits a weak dependence of composition on temperature (steep curve) above ∼10 °C, likely due to swelling and restructuring of the nonpolar nano-domains of the IL being limited by energetically unfavorable restructuring in the polar nano-domains. The solubility of the n-alkanes decreases with increasing size (molar volume), a trend that continues for the cyclic alkanes, for which upper critical solution temperatures are observed below 70 °C. 1-Octene is found to be more soluble than n-octane, attributable to a combination of its lower molar volume and slightly higher polarity. The COSMO-RS model is used to predict the T-x'-x'' diagrams and gives good qualitative agreement of the observed trends. This work presents the highest known solubility of n-alkanes in an IL to date and tuning the structure of the ionic liquid to maximize the size/shape trends observed may provide the basis for enhanced separations of nonpolar species.

  14. Combustion process for synthesis of carbon nanomaterials from liquid hydrocarbon

    DOEpatents

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

    2007-01-02

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

  15. Qualitative Analysis of Liquid Hydrocarbon Mixtures by Absorption Spectra of Their Vapors

    NASA Astrophysics Data System (ADS)

    Vesnin, V. L.

    2016-11-01

    Absorption spectra of saturated vapors of hydrocarbons and their mixtures were studied near their first overtones. Absorption spectra of hydrocarbons in the liquid and vapor states were compared. The ability to analyze qualitatively the compositions of liquid hydrocarbon mixtures using absorption spectra of their vapors was demonstrated. Indirect evidence suggested that the nonlinear absorption as a function of concentration that was seen in liquid hydrocarbon mixtures was negligible in their vapors.

  16. Two-step catalytic hydrodeoxygenation of fast pyrolysis oil to hydrocarbon liquid fuels.

    PubMed

    Xu, Xingmin; Zhang, Changsen; Liu, Yonggang; Zhai, Yunpu; Zhang, Ruiqin

    2013-10-01

    Two-step catalytic hydrodeoxygenation (HDO) of fast pyrolysis oil was investigated for translating pyrolysis oil to transportation grade hydrocarbon liquid fuels. At the first mild HDO step, various organic solvents were employed to promote HDO of bio-oil to overcome coke formation using noble catalyst (Ru/C) under mild conditions (300 °C, 10 MPa). At the second deep HDO step, conventional hydrogenation setup and catalyst (NiMo/Al2O3) were used under severe conditions (400 °C, 13 MPa) for obtaining hydrocarbon fuel. Results show that the phenomenon of coke formation is effectively eliminated, and the properties of products have been significantly improved, such as oxygen content decreases from 48 to 0.5 wt% and high heating value increases from 17 to 46 MJ kg(-1). GC-MS analysis indicates that the final products include C11-C27 aliphatic hydrocarbons and aromatic hydrocarbons. In short, the fast pyrolysis oils were successfully translated to hydrocarbon liquid fuels using a two-step catalytic HDO process.

  17. The dynamics of flash fires involving flammable hydrocarbon liquids.

    PubMed

    DeHaan, J D

    1996-03-01

    Victims of fires are sometimes discovered to have less-than-lethal levels of carbon monoxide (CO) in the blood and no significant antemortem fire damage. Such occurrences are often linked to flash fires involving volatile hydrocarbon fuels. In this study, the dynamics of hydrocarbon fuel fires are examined, and the results of fullscale room tests ignited with small (< 2 L) quantities of flammable liquid are found to confirm the theoretical predictions. These tests showed that flame plumes with temperatures of 500-975 degrees C were produced above flammable liquids. Ignition of their vapors in a carpeted room produced a very short-lived flash of fire throughout the room, followed by intense flames in a layer above the floor approximately 1 m deep, which quickly degenerated to isolated pools of low flames. Combustion of hydrocarbon vapors in a room caused oxygen levels to drop below 8.5% in < 100 s, while causing carbon dioxide (CO2) levels to increase to 12-16% whether the door to the room was open or closed. Production of CO trailed maximum CO2 production by 15-30 s. A victim exposed to such a fire may collapse from extreme heat (aided by the water vapor created by the combustion of hydrocarbons), weakened by oxygen deprivation, before CO inhalation becomes a significant factor.

  18. Short-Term Outlook for Hydrocarbon Gas Liquids

    EIA Publications

    2016-01-01

    U.S. liquid fuels production increased from 7.43 million barrels per day (b/d) in 2008 to 13.75 million b/d in 2015. However, the Short-Term Energy Outlook (STEO) expects liquid fuels production to decline to 12.99 million b/d in 2017, mainly as a result of prolonged low oil prices. The liquid fuels production forecast reflects a 1.24 million b/d decline in crude oil production by 2017 that is partially offset by a 450,000 b/d increase in the production of hydrocarbon gas liquids (HGL)—a group of products including ethane, propane, butane (normal and isobutane), natural gasoline, and refinery olefins. This analysis will discuss the outlook for each of these four HGL streams and related infrastructure projects through 2017.

  19. Short-Term Outlook for Hydrocarbon Gas Liquids

    EIA Publications

    2016-01-01

    U.S. liquid fuels production increased from 7.43 million barrels per day (b/d) in 2008 to 13.75 million b/d in 2015. However, the Short-Term Energy Outlook (STEO) expects liquid fuels production to decline to 12.99 million b/d in 2017, mainly as a result of prolonged low oil prices. The liquid fuels production forecast reflects a 1.24 million b/d decline in crude oil production by 2017 that is partially offset by a 450,000 b/d increase in the production of hydrocarbon gas liquids (HGL)—a group of products including ethane, propane, butane (normal and isobutane), natural gasoline, and refinery olefins. This analysis will discuss the outlook for each of these four HGL streams and related infrastructure projects through 2017.

  20. Hydrocarbon Gas Liquids (HGL): Recent Market Trends and Issues

    EIA Publications

    2014-01-01

    Over the past five years, rapid growth in U.S. onshore natural gas and oil production has led to increased volumes of natural gas plant liquids (NGPL) and liquefied refinery gases (LRG). The increasing economic importance of these volumes, as a result of their significant growth in production, has revealed the need for better data accuracy and transparency to improve the quality of historical data and projections for supply, demand, and prices of these liquids, co-products, and competing products. To reduce confusion in terminology and improve its presentation of data, EIA has worked with industry and federal and state governments to clarify gas liquid terminology and has developed the term Hydrocarbon Gas Liquids, or HGL.

  1. 30 CFR 250.1162 - When may I burn produced liquid hydrocarbons?

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 30 Mineral Resources 2 2011-07-01 2011-07-01 false When may I burn produced liquid hydrocarbons... SHELF Oil and Gas Production Requirements Flaring, Venting, and Burning Hydrocarbons § 250.1162 When may I burn produced liquid hydrocarbons? (a) You must request and receive approval from the Regional...

  2. Air-Liquid Interfaces: I. Alcohols and Aromatic Hydrocarbons

    NASA Astrophysics Data System (ADS)

    Allen, Heather; van Loon, Lisa; Hommel, Elizabeth

    2004-03-01

    Alcohols and aromatic hydrocarbons solutions were investigated using broad bandwidth sum frequency generation (BBSFG), a highly surface-selective spectroscopy, and IR and Raman spectroscopies. For aqueous methanol solutions the surface hydrogen bonding environment is quite different relative to the bulk environment. The surface BBSFG studies suggest that methanol is a more efficient hydrogen bonding acceptor when the methanol molecule resides in the interfacial region. Methanol reaction with sulfuric acid was also studied to quantify and understand the formation of mono methyl sulfonate relative to the dimethyl sulfonate. We have also investigated several neat and water-saturated liquid aromatic hydrocarbon surfaces. The data indicate that benzene and similar molecules are tilted at their air-liquid interface. With the introduction of relatively few water molecules into a 1-methyl naphthalene (1-MN) liquid (1 water: 336 1-MN) a rearrangement of the surface molecules is induced, leading to an increased number density of the methyl groups arranged such that more methyl groups are oriented in the same direction into the air phase at the air-liquid 1-MN interface.

  3. Liquid Oxygen Cooling of Hydrocarbon Fueled Rocket Thrust Chambers

    NASA Technical Reports Server (NTRS)

    Armstrong, Elizabeth S.

    1989-01-01

    Rocket engines using liquid oxygen (LOX) and hydrocarbon fuel as the propellants are being given serious consideration for future launch vehicle propulsion. Normally, the fuel is used to regeneratively cool the combustion chamber. However, hydrocarbons such as RP-1 are limited in their cooling capability. Another possibility for the coolant is the liquid oxygen. Combustion chambers previously tested with LOX and RP-1 as propellants and LOX as the collant demonstrated the feasibility of using liquid oxygen as a coolant up to a chamber pressure of 13.8 MPa (2000 psia). However, there was concern as to the effect on the integrity of the chamber liner if oxygen leaks into the combustion zone through fatigue cracks that may develop between the cooling passages and the hot gas side wall. In order to study this effect, chambers were fabricated with slots machined upstream of the throat between the cooling passage wall and the hot gas side wall to simulate cracks. The chambers were tested at a nominal chamber pressure of 8.6 MPa (1247 psia) over a range of mixture ratios from 1.9 to 3.1 using liquid oxygen as the coolant. The results of the testing showed that the leaking LOX did not have a deleterious effect on the chambers in the region of the slots. However, there was unexplained melting in the throat region of both chambers, but not in line with the slots.

  4. Liquid Chromatographic Determination of Explosives and Polynuclear Aromatic Hydrocarbons (PAHs) in Deactivation Furnace Ash.

    DTIC Science & Technology

    1986-08-01

    High performance liquid chromatography (HPLC) Polynuclear aromatic hydrocarbons (PAHs...chromatography or high performance liquid chromatography (HPLC). Gas chromatography (GC), because of its speed and sensitivity, has received much...Staley. 1976. Determination of polycyclic aromatic hydrocarbons in atmospheric particulate matter by high performance liquid chromatography coupled

  5. Interfacial Properties and Mechanisms Dominating Gas Hydrate Cohesion and Adhesion in Liquid and Vapor Hydrocarbon Phases.

    PubMed

    Hu, Sijia; Koh, Carolyn A

    2017-10-03

    The interfacial properties and mechanisms of gas hydrate systems play a major role in controlling their interparticle and surface interactions, which is desirable for nearly all energy applications of clathrate hydrates. In particular, preventing gas hydrate interparticle agglomeration and/or particle-surface deposition is critical to the prevention of gas hydrate blockages during the exploration and transportation of oil and gas subsea flow lines. These agglomeration and deposition processes are dominated by particle-particle cohesive forces and particle-surface adhesive force. In this study, we present the first direct measurements on the cohesive and adhesive forces studies of the CH4/C2H6 gas hydrate in a liquid hydrocarbon-dominated system utilizing a high-pressure micromechanical force (HP-MMF) apparatus. A CH4/C2H6 gas mixture was used as the gas hydrate former in the model liquid hydrocarbon phase. For the cohesive force baseline test, it was found that the addition of liquid hydrocarbon changed the interfacial tension and contact angle of water in the liquid hydrocarbon compared to water in the gas phase, resulting in a force of 23.5 ± 2.5 mN m(-1) at 3.45 MPa and 274 K for a 2 h annealing time period in which hydrate shell growth occurs. It was observed that the cohesive force was inversely proportional to the annealing time, whereas the force increased with increasing contact time. For a longer contact time (>12 h), the force could not be measured because the two hydrate particles adhered permanently to form one large particle. The particle-surface adhesive force in the model liquid hydrocarbon was measured to be 5.3 ± 1.1 mN m(-1) under the same experimental condition. Finally, with a 1 h contact time, the hydrate particle and the carbon steel (CS) surface were sintered together and the force was higher than what could be measured by the current apparatus. A possible mechanism is presented in this article to describe the effect of contact time on the

  6. A liquid hydrocarbon deuteron source for neutron generators

    NASA Astrophysics Data System (ADS)

    Schwoebel, P. R.

    2017-06-01

    Experimental studies of a deuteron spark source for neutron generators using hydrogen isotope fusion reactions are reported. The ion source uses a spark discharge between electrodes coated with a deuterated hydrocarbon liquid, here Santovac 5, to inhibit permanent electrode erosion and extend the lifetime of high-output neutron generator spark ion sources. Thompson parabola mass spectra show that principally hydrogen and deuterium ions are extracted from the ion source. Hydrogen is the chief residual gas phase species produced due to source operation in a stainless-steel vacuum chamber. The prominent features of the optical emission spectra of the discharge are C+ lines, the hydrogen Balmer Hα-line, and the C2 Swan bands. Operation of the ion source was studied in a conventional laboratory neutron generator. The source delivered an average deuteron current of ˜0.5 A nominal to the target in a 5 μs duration pulse at 1 Hz with target voltages of -80 to -100 kV. The thickness of the hydrocarbon liquid in the spark gap and the consistency thereof from spark to spark influences the deuteron yield and plays a role in determining the beam-focusing characteristics through the applied voltage necessary to break down the spark gap. Higher breakdown voltages result in larger ion beam spots on the target and vice-versa. Because the liquid self-heals and thereby inhibits permanent electrode erosion, the liquid-based source provides long life, with 104 pulses to date, and without clear evidence that, in principle, the lifetime could not be much longer. Initial experiments suggest that an alternative cylindrical target-type generator design can extract approximately 10 times the deuteron current from the source. Preliminary data using the deuterated source liquid as a neutron-producing target are also presented.

  7. Direct conversion of light hydrocarbon gases to liquid fuel

    SciTech Connect

    Foral, M.J.

    1990-01-01

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

  8. Direct conversion of light hydrocarbon gases to liquid fuel

    SciTech Connect

    Foral, M.J.

    1991-01-01

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

  9. Ballistic Evaporation and Solvation of Helium Atoms at the Surfaces of Protic and Hydrocarbon Liquids.

    PubMed

    Johnson, Alexis M; Lancaster, Diane K; Faust, Jennifer A; Hahn, Christine; Reznickova, Anna; Nathanson, Gilbert M

    2014-11-06

    Atomic and molecular solutes evaporate and dissolve by traversing an atomically thin boundary separating liquid and gas. Most solutes spend only short times in this interfacial region, making them difficult to observe. Experiments that monitor the velocities of evaporating species, however, can capture their final interactions with surface solvent molecules. We find that polarizable gases such as N2 and Ar evaporate from protic and hydrocarbon liquids with Maxwell-Boltzmann speed distributions. Surprisingly, the weakly interacting helium atom emerges from these liquids at high kinetic energies, exceeding the expected energy of evaporation from salty water by 70%. This super-Maxwellian evaporation implies in reverse that He atoms preferentially dissolve when they strike the surface at high energies, as if ballistically penetrating into the solvent. The evaporation energies increase with solvent surface tension, suggesting that He atoms require extra kinetic energy to navigate increasingly tortuous paths between surface molecules.

  10. Vapor condensation process produces slurry of magnesium particles in liquid hydrocarbons

    NASA Technical Reports Server (NTRS)

    Prok, G. M.; Walsh, T. J.; Witzke, W. R.

    1966-01-01

    Vapor condensation apparatus produces a physically stable, homogeneous slurry of finely divided magnesium and liquid hydrocarbons. The magnesium is vaporized and the resultant vapor is cooled rapidly with a liquid hydrocarbon spray, which also serves as the dispersing medium for the condensed magnesium particles.

  11. Development of an ionic liquid based dispersive liquid-liquid microextraction method for the analysis of polycyclic aromatic hydrocarbons in water samples.

    PubMed

    Pena, M Teresa; Casais, M Carmen; Mejuto, M Carmen; Cela, Rafael

    2009-09-04

    A simple, rapid and efficient method, ionic liquid based dispersive liquid-liquid microextraction (IL-DLLME), has been developed for the first time for the determination of 18 polycyclic aromatic hydrocarbons (PAHs) in water samples. The chemical affinity between the ionic liquid (1-octyl-3-methylimidazolium hexafluorophosphate) and the analytes permits the extraction of the PAHs from the sample matrix also allowing their preconcentration. Thus, this technique combines extraction and concentration of the analytes into one step and avoids using toxic chlorinated solvents. The factors affecting the extraction efficiency, such as the type and volume of ionic liquid, type and volume of disperser solvent, extraction time, dispersion stage, centrifuging time and ionic strength, were optimised. Analysis of extracts was performed by high performance liquid chromatography (HPLC) coupled with fluorescence detection (Flu). The optimised method exhibited a good precision level with relative standard deviation values between 1.2% and 5.7%. Quantification limits obtained for all of these considered compounds (between 0.1 and 7 ng L(-1)) were well below the limits recommended in the EU. The extraction yields for the different compounds obtained by IL-DLLME, ranged from 90.3% to 103.8%. Furthermore, high enrichment factors (301-346) were also achieved. The extraction efficiency of the optimised method is compared with that achieved by liquid-liquid extraction. Finally, the proposed method was successfully applied to the analysis of PAHs in real water samples (tap, bottled, fountain, well, river, rainwater, treated and raw wastewater).

  12. Total hydrocarbon content (THC) testing in liquid oxygen (LOX) systems

    NASA Astrophysics Data System (ADS)

    Meneghelli, B. J.; Obregon, R. E.; Ross, H. R.; Hebert, B. J.; Sass, J. P.; Dirschka, G. E.

    2015-12-01

    The measured Total Hydrocarbon Content (THC) levels in liquid oxygen (LOX) systems at Stennis Space Center (SSC) have shown wide variations. Examples of these variations include the following: 1) differences between vendor-supplied THC values and those obtained using standard SSC analysis procedures; and 2) increasing THC values over time at an active SSC test stand in both storage and run vessels. A detailed analysis of LOX sampling techniques, analytical instrumentation, and sampling procedures will be presented. Additional data obtained on LOX system operations and LOX delivery trailer THC values during the past 12-24 months will also be discussed. Field test results showing THC levels and the distribution of the THC's in the test stand run tank, modified for THC analysis via dip tubes, will be presented.

  13. Direct conversion of light hydrocarbon gases to liquid fuel

    SciTech Connect

    Foral, M.J.

    1990-01-01

    Amoco Oil Company is investigating the direct conversion of light hydrocarbon gases to liquid fuels via partial oxidation. This report describes work completed in the first quarter of the two-year project (first quarter FY 1990). Task 1 of the work, preparation of the Project Management Plan, has been completed. Work was started and progress made on three other tasks during this quarter: Task 2. Modification of an existing Amoco pilot plant to handle the conditions of this project. Minor modifications were made to increase the maximum operating pressure to 1500 psig. Other more extensive modifications are being designed, including addition of an oxygen compressor and recycle system. Task 3.1. Evaluation of a Los Alamos National Laboratory methane oxidation kinetic model for suitability in guiding the experimental portions of this project. Task 3.2. Process variable (e.g. temperature, pressure, residence time) studies to determine optimal partial oxidation conditions. 1 fig.

  14. Total Hydrocarbon Content (THC) Testing in Liquid Oxygen (LOX)

    NASA Technical Reports Server (NTRS)

    Meneghelli, B. J.; Obregon, R. E.; Ross, H. R.; Hebert, B. J.; Sass, J. P.; Dirschka, G. E.

    2016-01-01

    The measured Total Hydrocarbon Content (THC) levels in liquid oxygen (LOX) systems at Stennis Space Center (SSC) have shown wide variations. Examples of these variations include the following: 1) differences between vendor-supplied THC values and those obtained using standard SSC analysis procedures; and 2) increasing THC values over time at an active SSC test stand in both storage and run vessels. A detailed analysis of LOX sampling techniques, analytical instrumentation, and sampling procedures will be presented. Additional data obtained on LOX system operations and LOX delivery trailer THC values during the past 12-24 months will also be discussed. Field test results showing THC levels and the distribution of the THC's in the test stand run tank, modified for THC analysis via dip tubes, will be presented.

  15. Composition and concentrations of semi-volatile hydrocarbons. Final report

    SciTech Connect

    Zielinska, B.; Fung, K.; Sheetz, L.

    1992-08-01

    Nonmethane hydrocarbons (NMHC) in ambient air are routinely analyzed for C2 to C10 species. The Caldecott Tunnel, located in the San Francisco area, was selected as a site dominated by motor vehicle emissions. The remaining sampling sites were: Los Angeles as a typical urban site, and Oildale as a site dominated by oil production. Whole air samples, analyzed for C2 through C12 hydrocarbons, were collected using the stainless steel canisters. Semi-volatile hydrocarbons, in the range of C8 to C18, were collected using Tenax-TA solid adsorbent. The samples were analyzed using high resolution gas chromatographic separation and Fourier transform infrared/mass spectrometric detection (GC/IRD/MSD) or flame ionization detection (FID) of individual hydrocarbons. The comparison of hydrocarbon concentrations found in the Tenax and canister samples and the assessment of the levels of semivolatile hydrocarbons (C10-C18 range) relative to total non-methane hydrocarbons (C2-C10 or C2-C12), as measured by the canister method, is presented. The results showed that the percent contribution of SVHC to TNMHC ranged from approximately 1 to approximately 18% depending on the carbon number arbitrarily selected as a starting point of SVHC range.

  16. Removal of Mercury in Liquid Hydrocarbons using Zeolites Modified with Chitosan and Magnetic Iron Oxide Nanoparticles

    NASA Astrophysics Data System (ADS)

    Kusrini, E.; Susanto, B. H.; Nasution, D. A.; Jonathan, R.; Khairul, W. M.

    2017-07-01

    Clinoptilolite zeolites were chemically modified with chitosan (Chit) and magnetic iron oxide nanoparticles (Fe3O4NPs) were synthesized for removal of mercury from liquid condensate hydrocarbon. The mercury content was in liquid hydrocarbon which was measured by Lumex mercury analyzer. The performance of sorbents based on zeolites modified chitosan and magnetic nanoparticles were examined on the real liquid condensate hydrocarbon. Removal of mercury using a prestine clinoptilolite zeolites, and zeolites modified chitosan (zeolites-Chit) were ∼4.5, and ∼35%, respectively. The effects of magnetic nanoparticles in zeolites-Chit sorbents were significant to reduce the mercury content in liquid condensate hydrocarbon which were from ∼63 to ∼66%. Increasing the mass ratio of Fe3O4 that influenced to the BET surface area of natural zeolites. Zeolites-Chit-Fe3O4NPs as an efficient sorbents are potential ideal to remove mercury in hydrocarbon for practical applications.

  17. Influence of cation structure on binary liquid-liquid equilibria for systems containing ionic liquids based on trifluoromethanesulfonate anion with hydrocarbons.

    PubMed

    Marciniak, Andrzej; Karczemna, Ewa

    2010-04-29

    Binary liquid-liquid equilibria for 15 systems containing an ionic liquid (1-butyl-3-methylimidazolium trifluoromethanesulfonate, 1-butyl-3-methylpyridinium trifluoromethanesulfonate, 1-butyl-1-methylpyrrolidinium trifluoromethanesulfonate) with a hydrocarbon (n-hexane, n-heptane, cyclohexane, benzene, toluene) were measured by the dynamic method. The influence of cation structure of trifluoromethanesulfonate anion based ionic liquids on solubility of aliphatic and aromatic hydrocarbons is discussed.

  18. Performance comparison of autothermal reforming for liquid hydrocarbons, gasoline and diesel for fuel cell applications

    NASA Astrophysics Data System (ADS)

    Kang, Inyong; Bae, Joongmyeon; Bae, Gyujong

    This paper discusses the reforming of liquid hydrocarbons to produce hydrogen for fuel cell applications, focusing on gasoline and diesel due to their high hydrogen density and well-established infrastructures. Gasoline and diesel are composed of numerous hydrocarbon species including paraffins, olefins, cycloparaffins, and aromatics. We have investigated the reforming characteristics of several representative liquid hydrocarbons. In the case of paraffin reforming, H 2 yield and reforming efficiency were close to thermodynamic equilibrium status (TES), although heavier hydrocarbons required slightly higher temperatures than lighter hydrocarbons. However, the conversion efficiency was much lower for aromatics than paraffins with similar carbon number. We have also investigated the reforming performance of simulated commercial diesel and gasoline using simple synthetic diesel and gasoline compositions. Reforming performances of our formulations were in good agreement with those of commercial fuels. In addition, the reforming of gas to liquid (GTL) resulted in high H 2 yield and reforming efficiency showing promise for possible fuel cell applications.

  19. Reflectance spectra of three liquid hydrocarbons on a common sand type

    NASA Astrophysics Data System (ADS)

    Allen, C. Scott; Satterwhite, Melvin B.

    2006-05-01

    Three liquid hydrocarbons of different volatilities were incrementally applied to a quartz sand substrate. These liquids were gasoline, diesel fuel, and motor oil. The reflectance spectra of the hydrocarbon-sand samples varied directly with the amount (weight) of liquid on the sand. Liquid-saturated sand samples were then left to age in ambient, outdoor, environmental conditions. At regular intervals, the samples were re-measured for the residual liquid and the associated change in sample reflectance. The results outlined temporal windows of opportunity for detecting these products on the sand substrate. The windows ranged from less than 24-hours to more than a week, depending on liquid volatility. Each hydrocarbon darkened the sand and produced hydrocarbon absorption features near 1.70 and 2.31 μm and a hydrocarbon plateau at 2.28-2.45 μm. These features were used to differentiate the liquid-sand samples. A normalized difference index metric based on one of these features and a spectral continuum band described the reflectance-weight loss and reflectance-time relations. The normalized difference hydrocarbon index (NDHI) using the 1.60 and 2.31 μm bands best characterized the samples.

  20. Short-Term Energy Outlook Model Documentation: Hydrocarbon Gas Liquids Supply and Demand

    EIA Publications

    2015-01-01

    The hydrocarbon gas liquids (ethane, propane, butanes, and natural gasoline) module of the Short-Term Energy Outlook (STEO) model is designed to provide forecasts of U.S. production, consumption, refinery inputs, net imports, and inventories.

  1. Short-Term Energy Outlook Model Documentation: Hydrocarbon Gas Liquids Supply and Demand

    EIA Publications

    2015-01-01

    The hydrocarbon gas liquids (ethane, propane, butanes, and natural gasoline) module of the Short-Term Energy Outlook (STEO) model is designed to provide forecasts of U.S. production, consumption, refinery inputs, net imports, and inventories.

  2. Hydrocarbons and energy from plants: Final report, 1984-1987

    SciTech Connect

    Calvin, M.; Otvos, J.; Taylor, S.E.; Nemethy, E.K.; Skrukrud, C.L.; Hawkins, D.R.; Lago, R.

    1988-08-01

    Plant hydrocarbon (isoprenoid) production was investigated as an alternative source to fossil fuels. Because of their high triterpenoid (hydrocarbon) content of 4--8%, Euphorbia lathyris plants were used as a model system for this study. The structure of the E. lathyris triterpenoids was determined, and triterpenoid biosynthesis studied to better understand the metabolic regulation of isoprenoid production. Triterpenoid biosynthesis occurs in two distinct tissue types in E. lathyris plants: in the latex of the laticifer cells; and in the mesophyll cells of the leaf and stem. The latex has been fractionated by centrifugation, and it has been determined that the later steps of isoprenoid biosynthesis, the conversion of mevalonic acid to the triterpenes, are compartmentized within a vacuole. Also identified was the conversion of hydroxymethyl glutaryl-CoA to mevalonic acid, catalyzed by the enzyme Hydroxymethyl glutaryl-CoA Reductase, as a key rate limiting step in isoprenoid biosynthesis. At least two isozymes of this enzyme, one in the latex and another in the leaf plastids, have been identified. Environmental stress has been applied to plants to study changes in carbon allocation. Salinity stress caused a large decrease in growth, smaller decreases in photosynthesis, resulting in a larger allocation of carbon to both hydrocarbon and sugar production. An increase in Hydroxymethyl glutaryl-CoA Reductase activity was also observed when isoprenoid production increased. Other species where also screened for the production of hydrogen rich products such as isoprenoids and glycerides, and their hydrocarbon composition was determined.

  3. 30 CFR 250.1163 - How must I measure gas flaring or venting volumes and liquid hydrocarbon burning volumes, and...

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... volumes and liquid hydrocarbon burning volumes, and what records must I maintain? 250.1163 Section 250... Requirements Flaring, Venting, and Burning Hydrocarbons § 250.1163 How must I measure gas flaring or venting volumes and liquid hydrocarbon burning volumes, and what records must I maintain? (a) If your facility...

  4. 30 CFR 250.1163 - How must I measure gas flaring or venting volumes and liquid hydrocarbon burning volumes, and...

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... volumes and liquid hydrocarbon burning volumes, and what records must I maintain? 250.1163 Section 250... Requirements Flaring, Venting, and Burning Hydrocarbons § 250.1163 How must I measure gas flaring or venting volumes and liquid hydrocarbon burning volumes, and what records must I maintain? (a) If your facility...

  5. 30 CFR 250.1163 - How must I measure gas flaring or venting volumes and liquid hydrocarbon burning volumes, and...

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... volumes and liquid hydrocarbon burning volumes, and what records must I maintain? 250.1163 Section 250..., and Burning Hydrocarbons § 250.1163 How must I measure gas flaring or venting volumes and liquid hydrocarbon burning volumes, and what records must I maintain? (a) If your facility processes more than an...

  6. 30 CFR 250.1163 - How must I measure gas flaring or venting volumes and liquid hydrocarbon burning volumes, and...

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... volumes and liquid hydrocarbon burning volumes, and what records must I maintain? 250.1163 Section 250... Requirements Flaring, Venting, and Burning Hydrocarbons § 250.1163 How must I measure gas flaring or venting volumes and liquid hydrocarbon burning volumes, and what records must I maintain? (a) If your facility...

  7. 30 CFR 250.1163 - How must I measure gas flaring or venting volumes and liquid hydrocarbon burning volumes, and...

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... volumes and liquid hydrocarbon burning volumes, and what records must I maintain? 250.1163 Section 250... Production Requirements Flaring, Venting, and Burning Hydrocarbons § 250.1163 How must I measure gas flaring or venting volumes and liquid hydrocarbon burning volumes, and what records must I maintain? (a) If...

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

    SciTech Connect

    Professor Francisco Zaera

    2007-08-09

    production of small amounts of ethylene and water, most likely via the concerted decomposition or disproportionation of the adsorbed molecular species. The bulk of the 2-iodoethanol decomposes at about 150 K via an initial carbon-iodine scission to form –O(H)CH2CH2– (~80%) and 2-hydroxyethyl (~20%) intermediates. Two competing reactions are involved with the subsequent conversion of the 2-hydroxyethyl species around 160 K, a reductive elimination with surface hydrogen to yield ethanol, and a β-H elimination to surface vinyl alcohol. The –O(H)CH2CH2–, on the other hand, dehydrogenates to a –OCH2CH2– oxametallacycle species about the same temperature. Both 2-hydroxyethyl and oxametallacycle species tautomerize to acetaldehyde, around 210 K and above 250 K, respectively, and some of that acetaldehyde desorbs while the rest decomposes to hydrogen and carbon monoxide. We contend that a better understanding of the surface chemistry of oxygen-containing surfaces can lead to better selectivities in catalysis. This is arguably the most important issue in the field of catalysis in the near future, and one that impacts several technologies of interest to DOE such as the manufacturing of speciality chemicals and the control and removal of pollutants. Additional work was performed on the characterization of the chemistry of methyl and methylene adsorbed species on oxygen-treated nickel surfaces. Complex chemistry was observed involving not only hydrogenation and dehydrogenation steps, but also C-C couplings and methylene insertions to produce heavier hydrocarbons, and oxygen insertion reactions that yield oxygenates. Finally, a dual titration technique employing xenon and a chemically sensitive probe was developed to identify minority catalytic sites on oxide surfaces. In the case of oxygen-treated Ni(110) single crystals, it was found that both hydrogen transfer with adsorbed water or ammonia and certain hydrocarbon hydrogenation reactions take place at the end of the

  9. Methods of producing alkylated hydrocarbons from an in situ heat treatment process liquid

    DOEpatents

    Roes, Augustinus Wilhelmus Maria [Houston, TX; Mo, Weijian [Sugar Land, TX; Muylle, Michel Serge Marie [Houston, TX; Mandema, Remco Hugo [Houston, TX; Nair, Vijay [Katy, TX

    2009-09-01

    A method for producing alkylated hydrocarbons is disclosed. Formation fluid is produced from a subsurface in situ heat treatment process. The formation fluid is separated to produce a liquid stream and a first gas stream. The first gas stream includes olefins. The liquid stream is fractionated to produce at least a second gas stream including hydrocarbons having a carbon number of at least 3. The first gas stream and the second gas stream are introduced into an alkylation unit to produce alkylated hydrocarbons. At least a portion of the olefins in the first gas stream enhance alkylation.

  10. Ambient hydrocarbon and ozone concentrations near a refinery. Final report

    SciTech Connect

    Sexton, K.; Westberg, H.H.

    1983-04-01

    An ambient air monitoring study to characterize airborne emissions from petroleum refineries was conducted near the Marathon oil refinery at Robinson, Illinois during June 17 - July 29, 1977. Ground-level sampling facilities and an airplane equipped with air pollutant monitoring instruments provided an integrated, three-dimensional monitoring network. Measurements made during the study included ozone, oxides of nitrogen, sulfur dioxide, methane, carbon monoxide, individual C2-C10 hydrocarbons, halocarbons, condensation nuclei, visual distance and various meteorological parameters.

  11. Molecular catalytic hydrogenation of aromatic hydrocarbons and hydrotreating of coal liquids.

    SciTech Connect

    Yang, Shiyong; Stock, L.M.

    1996-05-01

    This report presents the results of research on the development of new catalytic pathways for the hydrogenation of multiring aromatic hydrocarbons and the hydrotreating of coal liquids at The University of Chicago under DOE Contract No. DE-AC22-91PC91056. The work, which is described in three parts, is primarily concerned with the research on the development of new catalytic systems for the hydrogenation of aromatic hydrocarbons and for the improvement of the quality of coal liquids by the addition of dihydrogen. Part A discusses the activation of dihydrogen by very basic molecular reagents to form adducts that can facilitate the reduction of multiring aromatic hydrocarbons. Part B examines the hydrotreating of coal liquids catalyzed by the same base-activated dihydrogen complexes. Part C concerns studies of molecular organometallic catalysts for the hydrogenation of monocyclic aromatic hydrocarbons under mild conditions.

  12. Liquid waste treatment system. Final report

    SciTech Connect

    Baker, M.N.; Houston, H.M.

    1999-06-01

    Pretreatment of high-level liquid radioactive waste (HLW) at the West Valley Demonstration Project (WVDP) involved three distinct processing operations: decontamination of liquid HLW in the Supernatant Treatment System (STS); volume reduction of decontaminated liquid in the Liquid Waste Treatment System (LWTS); and encapsulation of resulting concentrates into an approved cement waste form in the Cement Solidification System (CSS). Together, these systems and operations made up the Integrated Radwaste Treatment System (IRTS).

  13. Curable liquid hydrocarbon prepolymers containing hydroxyl groups and process for producing same

    NASA Technical Reports Server (NTRS)

    Rhein, R. A.; Ingham, J. D. (Inventor)

    1978-01-01

    Production of hydroxyl containing curable liquid hydrocarbon prepolymers by ozonizing a high molecular weight saturated hydrocarbon polymer such as polyisobutylene or ethylene propylene rubber is discussed. The ozonized material is reduced using reducing agents, preferably diisobutyl aluminum hydride, to form the hydroxyl containing liquid prepolymers having a substantially lower molecular weight than the parent polymer. The resulting curable liquid hydroxyl containing prepolymers can be poured into a mold and readily cured, with reactants such as toluene diisocyanate, to produce highly stable elastomers having a variety of uses such as binders for solid propellants.

  14. Toxicological profile for polycyclic aromatic hydrocarbons. Final report

    SciTech Connect

    Not Available

    1990-12-01

    The ATSDR Toxicological Profile for Polycyclic Aromatic Hydrocarbons (PAHs): Acenaphthene, Acenaphthylene, Anthracene, Benzo(a)anthracene, Benzo(a)pyrene, Benzo(b)fluoranthene, Benzo(g,h,i)perylene, Benzo(k)fluoranthene, Chrysene, Dibenzo(a,h)anthracene, Fluoranthene, Fluorene, Indeno(1,2,3-cd)pyrene, Phenanthrene, Pyrene is intended to characterize succinctly the toxicological and health effects information for the substance. It identifies and reviews the key literature that describes the substance's toxicological properties. Other literature is presented but described in less detail. The profile begins with a public health statement, which describes in nontechnical language the substance's relevant toxicological properties. The adequacy of information to determine the substance's health effects is described. Research gaps in nontoxic and health effects information are described. Research gaps that are of significance to the protection of public health will be identified in a separate effort. The focus of the document is on health and toxicological information.

  15. High energy decomposition of halogenated hydrocarbons FY93 final report

    SciTech Connect

    Mincher, B.J.; Arbon, R.E.; Meikrantz, D.H.

    1993-09-01

    The purpose of this program is to demonstrate a viable process for the decomposition of hazardous organochlorine compounds to nonhazardous products. This process has applicability to the treatment of mixed wastes containing both chlorinated hydrocarbons and radioactive constituents. The organics may be decomposed leaving only the radioactive constituents in the waste. Further, the use of spent nuclear fuel as a gamma-ray source presents a potentially cost effective energy source and elegantly allows the fuel to be considered a resource rather than a liability. During FY93 more than 400 samples were irradiated with fission product gamma-rays. Many of these samples were individual PCB congeners dissolved in isopropanol. These samples were studied to gain an understanding of the mechanism and kinetics of, and to provide a mass balance for, the PCB radiolysis reaction. In addition to research findings this report also contains a summary of efforts expended on technology transfer, professional publications and conference presentations.

  16. Liquid metal Flow Meter - Final Report

    SciTech Connect

    Andersen, C.; Hoogendoom, S.; Hudson, B.; Prince, J.; Teichert, K.; Wood, J.; Chase, K.

    2007-01-30

    Measuring the flow of liquid metal presents serious challenges. Current commercially-available flow meters use ultrasonic, electromagnetic, and other technologies to measure flow, but are inadequate for liquid metal flow measurement because of the high temperatures required by most liquid metals. As a result of the reactivity and high temperatures of most liquid metals, corrosion and leakage become very serious safety concerns. The purpose of this project is to develop a flow meter for Lockheed Martin that measures the flow rate of molten metal in a conduit.

  17. Biological upgrading of coal liquids. Final report

    SciTech Connect

    1995-02-01

    A large number of bacterial enrichments have been developed for their ability to utilize nitrogen and sulfur in coal liquids and the model compound naphtha. These bacteria include the original aerobic bacteria isolated from natural sources which utilize heteroatom compounds in the presence of rich media, aerobic nitrogen-utilizing bacteria and denitrifying bacteria. The most promising isolates include Mix M, a mixture of aerobic bacteria; ER15, a pyridine-utilizing isolate; ERI6, an aniline-utilizing isolate and a sewage sludge isolate. Culture optimization experiments have led to these bacteria being able to remove up to 40 percent of the sulfur and nitrogen in naphtha and coal liquids in batch culture. Continuous culture experiments showed that the coal liquid is too toxic to the bacteria to be fed without dilution or extraction. Thus either semi-batch operation must be employed with continuous gas sparging into a batch of liquid, or acid extracted coal liquid must be employed in continuous reactor studies with continuous liquid flow. Isolate EN-1, a chemical waste isolate, removed 27 percent of the sulfur and 19 percent of the nitrogen in fed batch experiments. Isolate ERI5 removed 28 percent of the nitrogen in coal liquid in 10 days in fed batch culture. The sewage sludge isolate removed 22.5 percent of the sulfur and 6.5 percent of the nitrogen from extracted coal liquid in continuous culture, and Mix M removed 17.5 percent of the nitrogen from medium containing extracted coal liquid. An economic evaluation has been prepared for the removal of nitrogen heteroatom compounds from Wilsonville coal liquid using acid extraction followed by fermentation. Similar technology can be developed for sulfur removal. The evaluation indicates that the nitrogen heteroatom compounds can be removed for $0.09/lb of coal liquid treated.

  18. Isotherms for adsorption of aromatic hydrocarbons from liquid paraffins on zeolites

    SciTech Connect

    Fominykh, L.F.; Abaimova, T.Ya.; Druzhkina, S.V.; Kondrat'ev, I.I.; Shevelev, Yu,V.

    1986-07-01

    This paper studies zeolite adsorption, under static conditions, of aromatic hydrocarbons from liquid paraffins obtained by the Parex method, and also the determination of adsorption isotherms. A weighed sample of the zeolite was activated in a muffle furnace at 450 C for 5 h and then cooled in a desiccator. The calculated values of the saturation adsorption of the hydrocarbons and the separation factor for the zeolites are listed.

  19. Developing Mathematical Provisions for Assessment of Liquid Hydrocarbon Emissions in Emergency Situations

    NASA Astrophysics Data System (ADS)

    Zemenkova, M. Yu; Zemenkov, Yu D.; Shantarin, V. D.

    2016-10-01

    The paper reviews the development of methodology for calculation of hydrocarbon emissions during seepage and evaporation to monitor the reliability and safety of hydrocarbon storage and transportation. The authors have analyzed existing methods, models and techniques for assessing the amount of evaporated oil. Models used for predicting the material balance of multicomponent two-phase systems have been discussed. The results of modeling the open-air hydrocarbon evaporation from an oil spill are provided and exemplified by an emergency pit. Dependences and systems of differential equations have been obtained to assess parameters of mass transfer from the open surface of a liquid multicomponent mixture.

  20. Liquid-state theory of hydrocarbon-water systems: Application to methane, ethane, and propane

    SciTech Connect

    Lue, L.; Blankschtein, D.

    1992-10-15

    The authors studied the structural and bulk thermodynamic properties of hydrocarbon (methane, ethane, and propane)-water systems as well as pure water using the site-site Ornstein-Zernike (SSOZ) equation under a variety of different closure relations in order to compare the quantitative predictive capabilities of the various closures. For the hydrocarbon-water systems, the simple point-charge(SPC) potential was used to model water, and the optimized potentials for liquid, simulation (OPLS) were used to model the hydrocarbons. 69 refs., 11 figs., 8 tabs.

  1. Influence of adhesion on aerobic biodegradation and bioremediation of liquid hydrocarbons.

    PubMed

    Abbasnezhad, Hassan; Gray, Murray; Foght, Julia M

    2011-11-01

    Biodegradation of poorly water-soluble liquid hydrocarbons is often limited by low availability of the substrate to microbes. Adhesion of microorganisms to an oil-water interface can enhance this availability, whereas detaching cells from the interface can reduce the rate of biodegradation. The capability of microbes to adhere to the interface is not limited to hydrocarbon degraders, nor is it the only mechanism to enable rapid uptake of hydrocarbons, but it represents a common strategy. This review of the literature indicates that microbial adhesion can benefit growth on and biodegradation of very poorly water-soluble hydrocarbons such as n-alkanes and large polycyclic aromatic hydrocarbons dissolved in a non-aqueous phase. Adhesion is particularly important when the hydrocarbons are not emulsified, giving limited interfacial area between the two liquid phases. When mixed communities are involved in biodegradation, the ability of cells to adhere to the interface can enable selective growth and enhance bioremediation with time. The critical challenge in understanding the relationship between growth rate and biodegradation rate for adherent bacteria is to accurately measure and observe the population that resides at the interface of the hydrocarbon phase. © Springer-Verlag 2011

  2. Hydrocarbon contamination increases the liquid water content of frozen Antarctic soils.

    PubMed

    Siciliano, Steven D; Schafer, Alexis N; Forgeron, Michelle A M; Snape, Ian

    2008-11-15

    We do not yet understand why fuel spills can cause greater damage in polar soils than in temperate soils. The role of water in the freezing environment may partly be responsible for why polar soils are more sensitive to pollution. We hypothesized that hydrocarbons alter the liquid water in frozen soil, and we evaluated this hypothesis by conducting laboratory and field experiments at Casey Station, Antarctica. Liquid water content in frozen soils (theta(liquid)) was estimated by time domain reflectometry in laboratory, field collected soils, and in situ field measurements. Our results demonstrate an increase in liquid water associated with hydrocarbon contamination in frozen soils. The dependence of theta(liquid) on aged fuel and spiked fuel were almost identical,with a slope of 2.6 x 10(-6) mg TPH (total petroleum hydrocarbons) kg(-1) for aged fuel and 3.1 x 10(-6) mg TPH kg(-1) for spiked fuel. In situ measurements found theta(liquid) depends, r2 = 0.75, on fuel for silt loam soils (theta(liquid) = 0.094 + 7.8 x 10(-6) mg TPH kg(-1)) but not on fuel for silt clay loam soils. In our study, theta(liquid) doubled in field soils and quadrupled in laboratory soils contaminated with diesel which may have profound implications on frost heave models in contaminated soils.

  3. Vortex-assisted extraction combined with dispersive liquid-liquid microextraction for the determination of polycyclic aromatic hydrocarbons in sediment by high performance liquid chromatography.

    PubMed

    Leng, Geng; Lui, Guibin; Chen, Yong; Yin, Hui; Dan, Dezhong

    2012-10-01

    A simple, rapid, and efficient method, vortex-assisted extraction followed by dispersive liquid-liquid microextraction (DLLME) has been developed for the extraction of polycyclic aromatic hydrocarbons (PAHs) in sediment samples prior to analysis by high performance liquid chromatography fluorescence detection. Acetonitrile was used as collecting solvent for the extraction of PAHs from sediment by vortex-assisted extraction. In DLLME, PAHs were rapidly transferred from acetonitrile to dichloromethane. Under the optimum conditions, the method yields a linear calibration curve in the concentration range from 10 to 2100 ng g(-1) for fluorene, anthracene, chrysene, benzo[k]fluoranthene, and benzo[a]pyrene, and 20 to 2100 ng g(-1) for other target analytes. Coefficients of determinations ranged from 0.9986 to 0.9994. The limits of detection, based on signal-to-noise ratio of three, ranged from 2.3 to 6.8 ng g(-1) . Reproducibility and recoveries was assessed by extracting a series of six independent sediment samples, which were spiked with different concentration levels. Finally, the proposed method was successfully applied in analyses of real nature sediment samples. The proposed method extended and improved the application of DLLME to solid samples, which greatly shorten the extraction time and simplified the extraction process.

  4. Catalytic oxidative desulfurization of liquid hydrocarbon fuels using air

    NASA Astrophysics Data System (ADS)

    Sundararaman, Ramanathan

    Conventional approaches to oxidative desulfurization of liquid hydrocarbons involve use of high-purity, expensive water soluble peroxide for oxidation of sulfur compounds followed by post-treatment for removal of oxidized sulfones by extraction. Both are associated with higher cost due to handling, storage of oxidants and yield loss with extraction and water separation, making the whole process more expensive. This thesis explores an oxidative desulfurization process using air as an oxidant followed by catalytic decomposition of sulfones thereby eliminating the aforementioned issues. Oxidation of sulfur compounds was realized by a two step process in which peroxides were first generated in-situ by catalytic air oxidation, followed by catalytic oxidation of S compounds using the peroxides generated in-situ completing the two step approach. By this technique it was feasible to oxidize over 90% of sulfur compounds present in real jet (520 ppmw S) and diesel (41 ppmw S) fuels. Screening of bulk and supported CuO based catalysts for peroxide generation using model aromatic compound representing diesel fuel showed that bulk CuO catalyst was more effective in producing peroxides with high yield and selectivity. Testing of three real diesel fuels obtained from different sources for air oxidation over bulk CuO catalyst showed different level of effectiveness for generating peroxides in-situ which was consistent with air oxidation of representative model aromatic compounds. Peroxides generated in-situ was then used as an oxidant to oxidize sulfur compounds present in the fuel over MoO3/SiO2 catalyst. 81% selectivity of peroxides for oxidation of sulfur compounds was observed on MoO3/SiO2 catalyst at 40 °C and under similar conditions MoO3/Al2O3 gave only 41% selectivity. This difference in selectivity might be related to the difference in the nature of active sites of MoO3 on SiO2 and Al2O 3 supports as suggested by H2-TPR and XRD analyses. Testing of supported and bulk Mg

  5. Standard test method for acidity of distillation residues or hydrocarbon liquids

    SciTech Connect

    Not Available

    1980-01-01

    This method covers the qualitative determination of the acidity of the distillation residue from a gasoline. The sample of distillation residue or hydrocarbon liquid is shaken with water and the aqueous layer tested for acidity to methyl orange. Some petroleum products are treated with mineral acid as part of the refining procedure. Obviously, any residual mineral acid in a petroleum product is undesirable. The absence of a positive indication in the test for acidity of the distillation residue or aqueous extract of a hydrocarbon liquid is an assurance of the care used in refining the fuel or solvent.

  6. Microwave plasmas generated in bubbles immersed in liquids for hydrocarbons reforming

    NASA Astrophysics Data System (ADS)

    Levko, Dmitry; Sharma, Ashish; Raja, Laxminarayan L.

    2016-06-01

    We present a computational modeling study of microwave plasma generated in cluster of atmospheric-pressure argon bubbles immersed in a liquid. We demonstrate that the use of microwaves allows the generation of a dense chemically active non-equilibrium plasma along the gas-liquid interface. Also, microwaves allow generation of overdense plasma in all the bubbles considered in the cluster which is possible because the collisional skin depth of the wave exceeds the bubble dimension. These features of microwave plasma generation in bubbles immersed in liquids are highly desirable for the large-scale liquid hydrocarbon reforming technologies.

  7. Liquid crystalline thermosetting polyimides. Final report

    SciTech Connect

    Hoyt, A.E.; Huang, S.J.

    1993-07-01

    Phase separation of rodlike reinforcing polymers and flexible coil matrix polymers is a common problem in formulating molecular composites. One way to reduce phase separation might be to employ liquid crystalline thermosets as the matrix material. In this work, functionally terminated polyimide oligomers which exhibit lyotropic liquid crystalline behavior were successfully prepared. Materials based on 2,2{prime}-bis(trifluoromethyl)-4,4{prime}-diaminobiphenyl and 3,3{prime},4,4{prime}-biphenylenetetra-carboxylic dianhydride have been synthesized and characterized.

  8. Chemical reduction of biomass polysaccharides to liquid hydrocarbon fuels

    SciTech Connect

    Robinson, J.M.; Alaniz, N.J.; Beech, D.J.

    1996-12-31

    Biomass is fractionated into the principle components cellulose (1), hemicellulose (2), and lignin (3). The two polysaccharide fractions 1 & 2 are converted into polyols by catalytic hydrogenation. Sorbitol, resulting from 1 for example, is treated sequentially with a redox coupled mixture of hydriodic acid and phosphorous acid and then with alcoholic base to afford a mixture of hydrocarbons including hexene. Step 2 of the process is highly tunable and can directly produce about 80% hydrocarbon oligomers, C{sub 12}H{sub 22} and C{sub 18}H{sub 32} and only about 20% of the intermediate 2-iodohexane. Recent results in the development of this new process will be presented. Oxygenate fuel additives, hexanols and hexyl ethers are also available by further reactions of hexene. These are presented in the accompanying paper.

  9. Method for direct conversion of gaseous hydrocarbons to liquids

    DOEpatents

    Kong, Peter C.; Lessing, Paul A.

    2006-03-07

    A chemical reactor for direct conversion of hydrocarbons includes a dielectric barrier discharge plasma cell and a solid oxide electrochemical cell in fluid communication therewith. The discharge plasma cell comprises a pair of electrodes separated by a dielectric material and passageway therebetween. The electrochemical cell comprises a mixed-conducting solid oxide electrolyte membrane tube positioned between a porous cathode and a porous anode, and a gas inlet tube for feeding oxygen containing gas to the porous cathode. An inlet is provided for feeding hydrocarbons to the passageway of the discharge plasma cell, and an outlet is provided for discharging reaction products from the reactor. A packed bed catalyst may optionally be used in the reactor to increase efficiency of conversion. The reactor can be modified to allow use of a light source for directing ultraviolet light into the discharge plasma cell and the electrochemical cell.

  10. Catalytic membrane reactor for conversion of syngas to liquid hydrocarbons

    SciTech Connect

    Khassin, A.A.

    2005-07-01

    Plug-through catalytically-active contractor membranes can combine high permeability ({gt} 20 m Darcy), high mechanical strength ({gt} 20 kg cm{sup -2}) and high heat-conductivity ({gt} 4 W(mK){sup -1}). Therefore, it provides isothermicity and low pressure drop. The intense mass-transfer within transport pores, high specific area of these pores and small distances between two adjacent transport pores weaken the mass-transfer constraints. Using the PCM one can achieve high space time yield of hydrocarbons and high selectivity towards heavy hydrocarbons and olefins. These advantages allow supposing the effective usage of the PCM catalytic membrane reactors in Fischer-Tropsch synthesis. Also the same approach could be efficient for some other multiphase catalytic processes, like hydrogenation of the unsaturated fatty acids. 5 figs.

  11. Catalysts and process for liquid hydrocarbon fuel production

    DOEpatents

    White, Mark G.; Ranaweera, Samantha A.; Henry, William P.

    2016-08-02

    The present invention provides a novel process and system in which a mixture of carbon monoxide and hydrogen synthesis gas, or syngas, is converted into hydrocarbon mixtures composed of high quality distillates, gasoline components, and lower molecular weight gaseous olefins in one reactor or step. The invention utilizes a novel supported bimetallic ion complex catalyst for conversion, and provides methods of preparing such novel catalysts and use of the novel catalysts in the process and system of the invention.

  12. Catalytic conversion of biomass-derived ethanol to liquid hydrocarbon blend-stock: Effect of light gas recirculation

    SciTech Connect

    Li, Zhenglong; Lepore, Andrew W.; Davison, Brian H.; Narula, Chaitanya K.

    2016-01-01

    Here, we describe a light gas recirculation (LGR) method to increase the liquid hydrocarbon yield with reduced aromatic content from catalytic conversion of ethanol to hydrocarbons. The previous liquid hydrocarbon yield is ~40% from one-pass ethanol conversion over V-ZSM-5 at 350 C and atmospheric pressure where the remaining ~60% yield is light gas hydrocarbons. In comparison, the liquid hydrocarbon yield increases to 80% when a simulated light gas hydrocarbon stream is co-fed at a rate of 0.053 mol g-1 h-1 with ethanol due to the conversion of most of the light olefins. The LGR also significantly improves the quality of the liquid hydrocarbon blend-stock by reducing aromatic content and overall benzene concentration. For 0.027 mol g-1 h-1 light gas mixture co-feeding, the average aromatic content in liquid hydrocarbons is 51.5% compared with 62.5% aromatic content in ethanol only experiment. Average benzene concentration decreases from 3.75% to 1.5% which is highly desirable since EPA limits benzene concentration in gasoline to 0.62%. As a result of low benzene concentration, the blend-wall for ethanol derived liquid hydrocarbons changes from ~18% to 43%. The remaining light paraffins and olefins can be further converted to valuable BTX products (94% BTX in the liquid) over Ga-ZSM-5 at 500 C. Thus, the LGR is an effective approach to convert ethanol to liquid hydrocarbons with higher liquid yield and low aromatic content, especially low benzene concentration, which could be blended with gasoline in a much higher ratio than ethanol or ethanol derived hydrocarbon blend-stock.

  13. Catalytic conversion of biomass-derived ethanol to liquid hydrocarbon blend-stock: Effect of light gas recirculation

    DOE PAGES

    Li, Zhenglong; Lepore, Andrew W.; Davison, Brian H.; ...

    2016-01-01

    Here, we describe a light gas recirculation (LGR) method to increase the liquid hydrocarbon yield with reduced aromatic content from catalytic conversion of ethanol to hydrocarbons. The previous liquid hydrocarbon yield is ~40% from one-pass ethanol conversion over V-ZSM-5 at 350 C and atmospheric pressure where the remaining ~60% yield is light gas hydrocarbons. In comparison, the liquid hydrocarbon yield increases to 80% when a simulated light gas hydrocarbon stream is co-fed at a rate of 0.053 mol g-1 h-1 with ethanol due to the conversion of most of the light olefins. The LGR also significantly improves the quality ofmore » the liquid hydrocarbon blend-stock by reducing aromatic content and overall benzene concentration. For 0.027 mol g-1 h-1 light gas mixture co-feeding, the average aromatic content in liquid hydrocarbons is 51.5% compared with 62.5% aromatic content in ethanol only experiment. Average benzene concentration decreases from 3.75% to 1.5% which is highly desirable since EPA limits benzene concentration in gasoline to 0.62%. As a result of low benzene concentration, the blend-wall for ethanol derived liquid hydrocarbons changes from ~18% to 43%. The remaining light paraffins and olefins can be further converted to valuable BTX products (94% BTX in the liquid) over Ga-ZSM-5 at 500 C. Thus, the LGR is an effective approach to convert ethanol to liquid hydrocarbons with higher liquid yield and low aromatic content, especially low benzene concentration, which could be blended with gasoline in a much higher ratio than ethanol or ethanol derived hydrocarbon blend-stock.« less

  14. Insertion of liquid crystal molecules into hydrocarbon monolayers

    SciTech Connect

    Popov, Piotr Mann, Elizabeth K.; Lacks, Daniel J.; Jákli, Antal

    2014-08-07

    Atomistic molecular dynamics simulations were carried out to investigate the molecular mechanisms of vertical surface alignment of liquid crystals. We study the insertion of nCB (4-Cyano-4{sup ′}-n-biphenyl) molecules with n = 0,…,6 into a bent-core liquid crystal monolayer that was recently found to provide good vertical alignment for liquid crystals. The results suggest a complex-free energy landscape for the liquid crystal within the layer. The preferred insertion direction of the nCB molecules (core or tail first) varies with n, which can be explained by entropic considerations. The role of the dipole moments was found to be negligible. As vertical alignment is the leading form of present day liquid crystal displays (LCD), these results will help guide improvement of the LCD technology, as well as lend insight into the more general problem of insertion of biological and other molecules into lipid and surfactant layers.

  15. Relation between liquid hydrocarbon reserves and geothermal gradients - Norwegian North Sea

    SciTech Connect

    Baird, R.A. )

    1991-03-01

    Comparison of average geothermal gradients and initial liquid hydrocarbon reserves for 28 Norwegian North Sea fields indicates that gradients in the largest North Sea oil fields cluster around 2.1F/100 feet. No reserves are found where gradients are lower than 1.8F/100 feet or higher than 2.3F/100 feet. At 6.89 billion barrels, reserves for 14 fields falling between 2.05 and 2.15/100 feet total over four times the reserves for all other fields put together. Reserves for seven fields at gradients lower than 2.05F/100 feet and for seven higher than 2.15F/100 feet total 594 and 991 million barrels, respectively. The conclusion is that 2.1F/100 feet is the optimum gradient for generation of liquid hydrocarbons in the Norwegian North Sea, given the depth, kerogen type, and source rock potential of the Kimmeridge Clay, the primary source rock there. Gradients lower than this have not stimulated maximum generation from the source rock. At higher gradients, increasing gas production from source rocks and thermal cracking of previously generated liquid hydrocarbons to gas are effective in limiting liquid hydrocarbon reserves. The 2.1F/100 feet gradient should be a useful pathfinder in the search for new oil reserves in the Norwegian North Sea. Determination of the optimum gradient should be a useful pathfinder in other regions as well.

  16. Catalysts and process for liquid hydrocarbon fuel production

    DOEpatents

    White, Mark G; Liu, Shetian

    2014-12-09

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

  17. Ionic Liquid Based Conversion of Biomass to Hydrocarbon Fuels

    DTIC Science & Technology

    2008-08-01

    out at 90 °C Task 2 - Investigation of the catalytic hydrolysis /depolymerization of cellulose in ionic liquid solvents. Ionic liquids possess...Office Cellulose is the most abundant form of living biomass on earth. It has been estimated that the annual photosynthetic production of cellulose is...stored energy (solid cellulose ) is not directly accessible to modern military systems. To utilize this energy requires the conversion of solid

  18. Final technical report for the Center for Catalytic Hydrocarbon Functionalization (an EFRC)

    SciTech Connect

    Gunnoe, Thomas Brent

    2016-11-11

    Greater than 95% of all materials produced by the chemical industry are derived from a small slate of simple hydrocarbons that are derived primarily from natural gas and petroleum, predominantly through oxygenation, C–C bond formation, halogenation or amination. Yet, current technologies for hydrocarbon conversion are typically high temperature, multi-step processes that are energy and capital intensive and result in excessive emissions (including carbon dioxide). The Center for Catalytic Hydrocarbon Functionalization (CCHF) brought together research teams with the broad coalition of skills and knowledge needed to make the fundamental advances in catalysis required for next-generation technologies to convert hydrocarbons (particularly light alkanes and methane) at high efficiency and low cost. Our new catalyst technologies offer many opportunities including enhanced utilization of natural gas in the transportation sector (via conversion to liquid fuels), more efficient generation of electricity from natural gas using direct methane fuel cells, reduced energy consumption and waste production for large petrochemical processes, and the preparation of high value molecules for use in biological/medical applications or the agricultural sector. The five year collaborative project accelerated fundamental understanding of catalyst design for the conversion of C–H bonds to functionalized products, essential to achieve the goals listed above, as evidenced by the publication of 134 manuscripts. Many of these fundamental advancements provide a foundation for potential commercialization, as evidenced by the submission of 11 patents from research support by the CCHF.

  19. Conversion of light hydrocarbon gases to metal carbides for production of liquid fuels and chemicals

    SciTech Connect

    Diaz, A.F.; Modestino, A.J.; Howard, J.B.; Peters, W.A.

    1993-02-01

    Light hydrocarbon gases could be reacted with low cost alkaline earth metal oxide (CaO, MgO) in high-temperature plasma reactor to achieve very high ([le]100%) gas conversion to H[sub 2], CO, and the corresponding metal carbides. These carbides could be stored, transported, and hydrolyzed to acetylene or methyl acetylene, which in turn could be upgraded to a wide range of chemicals and premium liquid hydrocarbon fuels. An electric arc discharge reactor was built for converting methane. Literature reviews were made.

  20. Process and catalyst for converting synthesis gas to liquid hydrocarbon mixture

    DOEpatents

    Rao, V. Udaya S.; Gormley, Robert J.

    1987-01-01

    Synthesis gas containing CO and H.sub.2 is converted to a high-octane hydrocarbon liquid in the gasoline boiling point range by bringing the gas into contact with a heterogeneous catalyst including, in physical mixture, a zeolite molecular sieve, cobalt at 6-20% by weight, and thoria at 0.5-3.9% by weight. The contacting occurs at a temperature of 250.degree.-300.degree. C., and a pressure of 10-30 atmospheres. The conditions can be selected to form a major portion of the hydrocarbon product in the gasoline boiling range with a research octane of more than 80 and less than 10% by weight aromatics.

  1. Crosslinked structurally-tuned polymeric ionic liquids as stationary phases for the analysis of hydrocarbons in kerosene and diesel fuels by comprehensive two-dimensional gas chromatography.

    PubMed

    Zhang, Cheng; Park, Rodney A; Anderson, Jared L

    2016-04-01

    Structurally-tuned ionic liquids (ILs) have been previously applied as the second dimension column in comprehensive two-dimensional gas chromatography (GC×GC) and have demonstrated high selectivity in the separation of individual aliphatic hydrocarbons from other aliphatic hydrocarbons. However, the maximum operating temperatures of these stationary phases limit the separation of analytes with high boiling points. In order to address this issue, a series of polymeric ionic liquid (PIL)-based stationary phases were prepared in this study using imidazolium-based IL monomers via in-column free radical polymerization. The IL monomers were functionalized with long alkyl chain substituents to provide the needed selectivity for the separation of aliphatic hydrocarbons. Columns were prepared with different film thicknesses to identify the best performing stationary phase for the separation of kerosene. The bis[(trifluoromethyl)sulfonyl]imide ([NTf2](-))-based PIL stationary phase with larger film thickness (0.28μm) exhibited higher selectivity for aliphatic hydrocarbons and showed a maximum allowable operating temperature of 300°C. PIL-based stationary phases containing varied amount of IL-based crosslinker were prepared to study the effect of the crosslinker on the selectivity and thermal stability of the resulting stationary phase. The optimal resolution of aliphatic hydrocarbons was achieved when 50% (w/w) of crosslinker was incorporated into the PIL-based stationary phase. The resulting stationary phase exhibited good selectivity for different groups of aliphatic hydrocarbons even after being conditioned at 325°C. Finally, the crosslinked PIL-based stationary phase was compared with SUPELCOWAX 10 and DB-17 columns for the separation of aliphatic hydrocarbons in diesel fuel. Better resolution of aliphatic hydrocarbons was obtained when employing the crosslinked PIL-based stationary phase as the second dimension column. Copyright © 2016 Elsevier B.V. All rights

  2. Final report on EURAMET.QM-S6/1195: Bilateral comparison of liquefied hydrocarbon mixtures in constant pressure (piston) cylinders

    NASA Astrophysics Data System (ADS)

    Brown, Andrew S.; Downey, Michael L.; Milton, Martin J. T.; van der Veen, Adriaan M. H.; Zalewska, Ewelina T.; Li, Jianrong

    2013-01-01

    Traceable liquid hydrocarbon mixtures are required in order to underpin measurements of the composition and other physical properties of LPG (liquefied petroleum gas) and LNG (liquefied natural gas), thus meeting the needs of an increasingly large European industrial market. The development of traceable liquid hydrocarbon standards by National Measurement Institutes (NMIs) was still at a relatively early stage at the time this comparison was proposed in 2011. NPL and VSL, who were the only NMIs active in this area, had developed methods for the preparation and analysis of such standards in constant pressure (piston) cylinders, but neither laboratory had Calibration and Measurement Capabilities (CMCs) for these mixtures. This report presents the results of EURAMET 1195, the first comparison of liquid hydrocarbon mixtures between NMIs, which assessed the preparation and analytical capabilities of NPL and VSL for these mixtures. The comparison operated between August 2011 and January 2012. Each laboratory prepared a liquid hydrocarbon standard with nominally the same composition and these standards were exchanged for analysis. The results of the comparison show a good agreement between the laboratories' results and the comparison reference values for the six components with amount fractions greater than 1.0 cmol/mol (propane, propene, iso-butene, n-butane, iso-butane and 1-butene). Measurement of the three components with lower amount fractions (1,3-butadiene, iso-pentane and n-pentane) proved more challenging. In all but one case, the differences from the comparison reference values for these three components were greater than the expanded measurement uncertainty. Main text. To reach the main text of this paper, click on Final Report. Note that this text is that which appears in Appendix B of the BIPM key comparison database kcdb.bipm.org/. The final report has been peer-reviewed and approved for publication by EURAMET, according to the provisions of the CIPM Mutual

  3. Hydroconversion of liquid hydrocarbons in a staged autothermal reactor

    SciTech Connect

    Blass, SD; Bhan, A; Schmidt, LD

    2013-01-31

    An autothermal staged reactor was assembled containing a top stage of Rh-Ce/alpha-Al2O3 which generated heat and H-2 by reacting CH4 and air that passed through a downstream stage containing 0.5 wt% Pt/gamma-Al2O3 mixed with either HBEA, HZSM-5, or USY in a heat-integrated non-isothermal reactor. The H-2 produced subsequently reacts in a 20:1 ratio with a co-feed of hexane or decane or 2-decanone fed to the reactor between the stages. The large-sized pores of HBEA and USY allowed deoxygenation of 2-decanone to form decene isomers which can crack or cyclize to form up to a 36% yield of methylated and ethylated monoaromatics. The medium-sized pores of HZSM-5 restricted decene formation from 2-decanone by catalyzing cracking reactions to C2-6 compounds which can cyclize to form aromatics. By contrast, the reactor effluent from non-oxygenated reactants decane and hexane contained less than 5% aromatics. Thus, we extend the scope of staged autothermal reactor functionality to hydrocracking and hydroisomerization of higher saturated and oxygenated hydrocarbons. (C) 2012 Elsevier B.V. All rights reserved.

  4. Infrared Study of Liquid / Solid Hydrocarbons and their Mixtures under Titan Conditions

    NASA Astrophysics Data System (ADS)

    Singh, Sandeep; Chevrier, V.; Roe, L.; Luspay-Kuti, A.; Wagner, A.

    2013-10-01

    This study presents the first experimental investigation of the infrared properties of hydrocarbons under Titan simulated conditions. Infrared spectra of liquid and solid CH4, C2H6 and their mixtures are taken to characterize infrared properties of Titan’s liquid and solids. We also monitor continuous change in mass of the compounds to emphasize the presence or absence of these compounds during evaporation/sublimation processes which are also quantified using IR spectra. Using our experimental evaporation/sublimation rates in the liquid-liquid and solid-liquid hydrocarbon mixtures we can determine the amount of CH4 that accumulates in the arid equatorial regions to produce liquid flows. Dark patches in the surface reflectance at 2 and 5 µm have been observed by Cassini spacecraft as seasonal formation of hydrocarbons lakes through a CH4 cycle. Identification of solid versus liquid phase states of CH4 and C2H6 on Titan requires laboratory measurements at relevant temperatures. The results for both CH4 and C2H6, reflectivity change as their phase changes from liquid to solid. In CH4 the band-depth of absorption bands decrease over time due to sublimation. Whereas in ethane, the band-depth is increasing over time due to its non-volatile nature. We have also investigated C2H2, as it was detected on the surface of Titan by the infrared spectrum in two of VIMS atmospheric windows at 1.54 µm and in the 2 µm region. The absorption features seen in the laboratory spectra are large enough to be potentially detected in VIMS. Currently, the solubility experiments of C2H2, CH3CN, and C4H10 in liquid CH4 and C2H6 are undergoing in our lab at 94 K and 1.5 bar. Since the amount of C2H2 present in Titan lakes can be several times the atmospheric amount, and is thought to be major soluble component in Titan lakes. We can correlate the laboratory experiments to the evaporites detected on the shoreline of Ontario Lacus by Cassini VIMS. Analyzing the Infrared spectra of the liquid-liquid

  5. Influence of brine-hydrocarbon interactions on FT-IR microspectroscopic analyses of intracrystalline liquid inclusions

    NASA Astrophysics Data System (ADS)

    Pironon, Jacques; Barrès, Odile

    1992-01-01

    Hydrocarbon droplets surrounded by an aqueous phase and trapped in a host crystal (i.e., fluid inclusions) are windows to the migrating hydrocarbon-water emulsions in petroleum reservoirs. Using synthetic hydrocarbon inclusions, Fourier transform infrared microspectrometric analysis shows that the interactions at the two liquid (hydrocarbon-aqueous solution) phase interface can be determined on a 20 μm scale. Spectral deformation, observed for the CH stretching bands, disappears when the alkali salt concentration decreases, when the organic solvent (CCl 4 or C 6H 6) concentration increases, and when the μFT-IR analysis point moves off the interface. This deformation is due to the cation effect on the interaction of the OH/CH dipoles. The Na +, K + cations break the water structure and induce modifications to the OH dipole at the interface, which then modifies the CH dipole moment and the CH stretching band intensity. Knowledge of the salinity of the aqueous phase is essential for complete understanding of infrared microanalysis of hydrocarbon fluid inclusions.

  6. Hydrocarbonoclastic biofilms based on sewage microorganisms and their application in hydrocarbon removal in liquid wastes.

    PubMed

    Al-Mailem, D M; Kansour, M K; Radwan, S S

    2014-07-01

    Attempts to establish hydrocarbonoclastic biofilms that could be applied in waste-hydrocarbon removal are still very rare. In this work, biofilms containing hydrocarbonoclastic bacteria were successfully established on glass slides by submerging them in oil-free and oil-containing sewage effluent for 1 month. Culture-dependent analysis of hydrocarbonoclastic bacterial communities in the biofilms revealed the occurrence of the genera Pseudomonas, Microvirga, Stenotrophomonas, Mycobacterium, Bosea, and Ancylobacter. Biofilms established in oil-containing effluent contained more hydrocarbonoclastic bacteria than those established in oil-free effluent, and both biofilms had dramatically different bacterial composition. Culture-independent analysis of the bacterial flora revealed a bacterial community structure totally different from that determined by the culture-dependent method. In microcosm experiments, these biofilms, when used as inocula, removed between 20% and 65% crude oil, n-hexadecane, and phenanthrene from the surrounding effluent in 2 weeks, depending on the biofilm type, the hydrocarbon identity, and the culture conditions. More of the hydrocarbons were removed by biofilms established in oil-containing effluent than by those established in oil-free effluent, and by cultures incubated in the light than by those incubated in the dark. Meanwhile, the bacterial numbers and diversities were enhanced in the biofilms that had been previously used in hydrocarbon bioremediation. These novel findings pave a new way for biofilm-based hydrocarbon bioremediation, both in sewage effluent and in other liquid wastes.

  7. Dielectric constant of liquid alkanes and hydrocarbon mixtures

    NASA Technical Reports Server (NTRS)

    Sen, A. D.; Anicich, V. G.; Arakelian, T.

    1992-01-01

    The complex dielectric constants of n-alkanes with two to seven carbon atoms have been measured. The measurements were conducted using a slotted-line technique at 1.2 GHz and at atmospheric pressure. The temperature was varied from the melting point to the boiling point of the respective alkanes. The real part of the dielectric constant was found to decrease with increasing temperature and correlate with the change in the molar volume. An upper limit to all the loss tangents was established at 0.001. The complex dielectric constants of a few mixtures of liquid alkanes were also measured at room temperature. For a pentane-octane mixture the real part of the dielectric constant could be explained by the Clausius-Mosotti theory. For the mixtures of n-hexane-ethylacetate and n-hexane-acetone the real part of the dielectric constants could be explained by the Onsager theory extended to mixtures. The dielectric constant of the n-hexane-acetone mixture displayed deviations from the Onsager theory at the highest fractions of acetone. The dipole moments of ethylacetate and acetone were determined for dilute mixtures using the Onsager theory and were found to be in agreement with their accepted gas-phase values. The loss tangents of the mixtures exhibited a linear relationship with the volume fraction for low concentrations of the polar liquids.

  8. Dielectric constant of liquid alkanes and hydrocarbon mixtures.

    PubMed

    Sen, A D; Anicich, V G; Arakelian, T

    1992-01-01

    The complex dielectric constants of n-alkanes with two to seven carbon atoms have been measured. The measurements were conducted using a slotted-line technique at 1.2 GHz and at atmospheric pressure. The temperature was varied from the melting point to the boiling point of the respective alkanes. The real part of the dielectric constant was found to decrease with increasing temperature and correlate with the change in the molar volume. An upper limit to all the loss tangents was established at 0.001. The complex dielectric constants of a few mixtures of liquid alkanes were also measured at room temperature. For a pentane-octane mixture the real part of the dielectric constant could be explained by the Clausius-Mosotti theory. For the mixtures of n-hexane-ethylacetate and n-hexane-acetone the real part of the dielectric constants could be explained by the Onsager theory extended to mixtures. The dielectric constant of the n-hexane-acetone mixture displayed deviations from the Onsager theory at the highest fractions of acetone. The dipole moments of ethylacetate and acetone were determined for dilute mixtures using the Onsager theory and were found to be in agreement with their accepted gas-phase values. The loss tangents of the mixtures exhibited a linear relationship with the volume fraction for low concentrations of the polar liquids.

  9. Dielectric constant of liquid alkanes and hydrocarbon mixtures

    NASA Technical Reports Server (NTRS)

    Sen, A. D.; Anicich, V. G.; Arakelian, T.

    1992-01-01

    The complex dielectric constants of n-alkanes with two to seven carbon atoms have been measured. The measurements were conducted using a slotted-line technique at 1.2 GHz and at atmospheric pressure. The temperature was varied from the melting point to the boiling point of the respective alkanes. The real part of the dielectric constant was found to decrease with increasing temperature and correlate with the change in the molar volume. An upper limit to all the loss tangents was established at 0.001. The complex dielectric constants of a few mixtures of liquid alkanes were also measured at room temperature. For a pentane-octane mixture the real part of the dielectric constant could be explained by the Clausius-Mosotti theory. For the mixtures of n-hexane-ethylacetate and n-hexane-acetone the real part of the dielectric constants could be explained by the Onsager theory extended to mixtures. The dielectric constant of the n-hexane-acetone mixture displayed deviations from the Onsager theory at the highest fractions of acetone. The dipole moments of ethylacetate and acetone were determined for dilute mixtures using the Onsager theory and were found to be in agreement with their accepted gas-phase values. The loss tangents of the mixtures exhibited a linear relationship with the volume fraction for low concentrations of the polar liquids.

  10. The Use of a Flash Vaporization System With Liquid Hydrocarbon Fuels in a Pulse Detonation Engine

    DTIC Science & Technology

    2004-01-01

    Peng , D . Y ., and Robinson , D . B ., “A New Two-Constant Equation of State,” Ind . Eng . Chem ., Fundam ...msec) Pr es su re ( b ar ) Manifold Pressure Head Pressure Figure 4. Premixed manifold and head pressure traces (absolute) for 15 Hz test...program uses the thermo physical properties of hydrocarbon mixtures database and computes the vapor-liquid equilibrium using the Peng - Robinson

  11. Hydrocarbon group type determination in jet fuels by high performance liquid chromatography

    NASA Technical Reports Server (NTRS)

    Antoine, A. C.

    1977-01-01

    Thirty-two jet and diesel fuel samples of varying chemical composition and physical properties were prepared from oil shale and coal syncrudes. Hydrocarbon types in these samples were determined by a fluorescent indicator adsorption analysis, and the results from three laboratories are presented and compared. Two methods of rapid high performance liquid chromatography were used to analyze some of the samples, and these results are also presented and compared. Two samples of petroleum-based Jet A fuel are similarly analyzed.

  12. Polycyclic Aromatic Hydrocarbons in Fine Particulate Matter Emitted from Burning Kerosene, Liquid Petroleum Gas, and Wood Fuels in Household Cookstoves

    EPA Science Inventory

    This study measured polycyclic aromatic hydrocarbon (PAH) composition in particulate matter emissions from residential cookstoves. A variety of fuel and cookstove combinations were examined, including: (i) liquid petroleum gas (LPG), (ii) kerosene in a wick stove, (iii) wood (10%...

  13. Radical cations in radiation chemistry of liquid hydrocarbons

    SciTech Connect

    Trifunac, A.D.; Sauer, M.C., Jr.; Shkrob, I.A.; Werst, D.W.

    1996-07-01

    The state of knowledge concerning radical cations in liquid alkanes is discussed with particular emphasis on those which exhibit high mobility. Uncertainty has existed in the interpretation of previous results with respect to the nature and reactivity of high mobility ions, especially for cyclohexane. Recent time-resolved studies on pulse radiolysis/transient absorption, photoconductivity, and magnetic resonance in these systems have led us to propose new mechanisms for the high mobility ions. In decalins, scavenging of these ions by solutes is a pseudo-first-order reaction. In cyclohexane, the behavior is more complex and is indicative of the involvement of two species. This bimodality is rationalized in terms of a dynamic equilibrium between two conformers of the solvent radical cation. Several experimental tests supporting these views include a recent study on two-color laser photoionization in cyclohexane.

  14. Detection of radiation-induced hydrocarbons in baked sponged cake prepared with irradiated liquid egg

    NASA Astrophysics Data System (ADS)

    Schulzki, G.; Spiegelberg, A.; Bögl, K. W.; Schreiber, G. A.

    1995-02-01

    For identification of irradiated food, radiation-induced volatile hydrocarbons (HC) are determined by gas chromatography in the non-polar fraction of fat. However, in complex food matrices the detection is often disturbed by fat-associated compounds. On-line coupling of high performance liquid chromatography (LC) and gas chromatography (GC) is very efficient to remove such compounds from the HC fraction. The high sensitivity of this fast and efficient technique is demonstrated by the example of detection of radiation-induced HC in fat isolated from baked sponge cake which had been prepared with irradiated liquid egg.

  15. Liquid Effluent Retention Facility (LERF) Final Hazard Category Determination

    SciTech Connect

    HUTH, L.L.

    2001-06-06

    The Liquid Effluent Retention Facility was designed to store 242-A Evaporator process condensate and other liquid waste streams for treatment at the 200 East Area Effluent Treatment Facility. The Liquid Effluent Retention Facility has been previously classified as a Category 3 Nonreactor Nuclear Facility. As defined in Hazard Categorization and Accident Analysis Techniques for Compliance with DOE Order 5480.23, Nuclear Safety Analysis Reports (DOE 1992, DOE 1997), Category 3 Nuclear Facilities have the potential for significant localized (radiological) consequences. However, based on current facility design, operations, and radioactive constituent concentrations, the Liquid Effluent Retention Facility does not have the potential for significant localized (radiological) consequences and is categorized as a Radiological Facility. This report documents the final hazard categorization process performed in accordance with DOE Order 5480.23, Nuclear Safety Analysis Reports. This report describes the current configuration and operations of the Liquid Effluent Retention Facility. Also included is a preliminary hazard categorization, which is based on current and proposed radioactive and hazardous material inventories, a preliminary hazards and accident analysis, and a final hazard category determination. The results of the hazards and accident analysis, based on the current configuration and operations of the Liquid Effluent Retention Facility and the current and proposed radioactive and hazardous material inventories, demonstrate that the Liquid Effluent Retention Facility does not have the potential for significant localized (radiological) consequences. Based on the final hazard category analysis, the Liquid Effluent Retention Facility is a Radiological Facility. The final hazard category determination is based on a comparative evaluation of the consequence basis for the Category 3 threshold quantities to the calculated consequences for credible releases The basis for

  16. Development of a dispersive liquid-liquid microextraction method using a lighter-than-water ionic liquid for the analysis of polycyclic aromatic hydrocarbons in water.

    PubMed

    Medina, Giselle S; Reta, Mario

    2016-11-01

    A dispersive liquid-liquid microextraction method using a lighter-than-water phosphonium-based ionic liquid for the extraction of 16 polycyclic aromatic hydrocarbons from water samples has been developed. The extracted compounds were analyzed by liquid chromatography coupled to fluorescence/diode array detectors. The effects of several experimental parameters on the extraction efficiency, such as type and volume of ionic liquid and disperser solvent, type and concentration of salt in the aqueous phase and extraction time, were investigated and optimized. Three phosphonium-based ionic liquids were assayed, obtaining larger extraction efficiencies when trihexyl-(tetradecyl)phosphonium bromide was used. The optimized methodology requires a few microliters of a lighter-than-water phosphonium-based ionic liquid, which allows an easy separation of the extraction solvent phase. The obtained limits of detection were between 0.02 and 0.56 μg/L, enrichment factors between 109 and 228, recoveries between 60 and 108%, trueness between 0.4 and 9.9% and reproducibility values between 3 and 12% were obtained. These figures of merit combined with the simplicity, rapidity and low cost of the analytical methodology indicate that this is a viable and convenient alternative to the methods reported in the literature. The developed method was used to analyze polycyclic aromatic hydrocarbons in river water samples.

  17. Valorization of biogas into liquid hydrocarbons in plasma-catalyst reactor

    NASA Astrophysics Data System (ADS)

    Nikravech, Mehrdad; Rahmani, Abdelkader; Labidi, Sana; Saintini, Noiric

    2016-09-01

    Biogas represents an important source of renewable energy issued from biological degradation of biomass. It is planned to produce in Europe the amount of biogas equivalent to 6400 kWh electricity and 4500 kteo (kilo tons equivalent oil) in 2020. Currently the biogas is used in cogeneration engines to produce heat and electricity directly in farms or it is injected in gas networks after purification and odorisation. The aim of this work is to propose a third option that consists of valorization of biogas by transformation into liquid hydrocarbons like acetone, methanol, ethanol, acetic acid etc. These chemicals, among the most important feed materials for chemical industries, retain CO2 molecules participating to reduce the greenhouse gas emissions and have high storage energy capacity. We developed a low temperature atmospheric plasma-catalyst reactor (surface dielectric barrier discharge) to transform biogas into chemicals. The conversion rates of CH4 and CO2 are respectively about 50% and 30% depending on operational conditions. The energetic cost is 25 eV/molecule. The yields of liquid hydrocarbon reaches currently 10% wt. More the 11 liquid chemicals are observed in the liquid fraction. Acknowledgements are due to SPC Programme Energie de demain.

  18. Liquid Hydrocarbons on Titan's Surface? How Cassini ISS Observations Fit into the Story (So Far)

    NASA Technical Reports Server (NTRS)

    Turtle, E. P.; Dawson, D. D.; Fussner, S.; Hardegree-Ullman, E.; Ewen, A. S.; Perry, J.; Porco, C. C.; West, R. A.

    2005-01-01

    Titan is the only satellite in our Solar System with a substantial atmosphere, the origins and evolution of which are still not well understood. Its primary (greater than 90%) component is nitrogen, with a few percent methane and lesser amounts of other species. Methane and ethane are stable in the liquid state under the temperature and pressure conditions in Titan s lower atmosphere and at the surface; indeed, clouds, likely composed of methane, have been detected. Photochemical processes acting in the atmosphere convert methane into more complex hydrocarbons, creating Titan s haze and destroying methane over relatively short timescales. Therefore, it has been hypothesized that Titan s surface has reservoirs of liquid methane which serve to resupply the atmosphere. Early observations of Titan s surface revealed albedo patterns which have been interpreted as dark hydrocarbon liquids occupying topographically low regions between higher-standing exposures of bright, water-ice bedrock, although this is far from being the only explanation for the observed albedo contrast. Observations made by the Imaging Science Subsystem during Cassini's approach to Saturn and its first encounters with Titan show the bright and dark regions in greater detail but have yet to resolve the question of whether there are liquids on the surface.

  19. Fluorocarbon and hydrocarbon N-heterocyclic (C5-C7) imidazole-based liquid crystals.

    PubMed

    Chen, Hongren; Hong, Fengying; Shao, Guang; Hang, Deyu; Zhao, Lei; Zeng, Zhuo

    2014-12-01

    By using three synthetic protocols, a series of fluorocarbon and hydrocarbon N-heterocyclic imidazole-based liquid crystals (LCs) and related imidazolium-based ionic liquid crystals (ILCs) have been prepared. The ring size of the N-heterocycle and the length of the N-terminal chain (on the imidazolium unit in the ILCs) were modified, and the influence of these structural parameters on liquid-crystal phases was investigated by means of polarizing optical microscopy (POM), differential scanning calorimetry (DSC), and X-ray diffraction (XRD). These new ILCs exhibit a disordered smectic phase (SmA), good thermal stabilities, a broad smectic phase range, a high dipole moment, relatively low melting points, but high clearing points and strong emission fluorescence relative to imidazole-based LCs. These encouraging results have led us to believe these fluorocarbon and hydrocarbon N-heterocyclic imidazole-based LCs and related imidazolium-based ILCs could be used as new liquid-crystalline materials.

  20. Hydrotreating the bitumen-derived hydrocarbon liquid produced in a fluidized-bed pyrolysis reactor

    SciTech Connect

    Longstaff, D.C.; Deo, M.D.; Hanson, F.V.; Oblad, A.G.; Tsai, C.H.

    1991-12-31

    The pyrolysis of bitumen-impregnated sandstone produces three primary product streams: C{sub 1}-C{sub 4} hydrocarbons gases, a C{sub 5}{sup +} total liquid product, and a carbonaceous residue on the spent sand. The bitumen-derived hydrocarbon liquid was significantly upgraded relative to the native bitumen: it had a higher API gravity, lower Conradson carbon residue, asphaltene content, pour point and viscosity and a reduced distillation endpoint relative to the native bitumen. The elemental composition was little different from that of the native bitumen except for the hydrogen content which was lower. The bitumen-derived liquid produced in a 4-inch diameter fluidized-bed reactor from the Whiterocks tar sand deposit has been hydrotreated in a fixed-bed reactor to determine the extent of upgrading as a function of process operating variables. The extent of denitrogenation and desulfurization of the bitumen-derived liquid was used to monitor catalyst activity as a function of process operating variables and to estimate the extent of catalyst deactivation as a function of time on-stream. The apparent kinetics for the nitrogen and sulfur removal reactions were determined. Product distribution and yield data were also obtained.

  1. Hydrotreating the bitumen-derived hydrocarbon liquid produced in a fluidized-bed pyrolysis reactor

    SciTech Connect

    Longstaff, D.C.; Deo, M.D.; Hanson, F.V.; Oblad, A.G.; Tsai, C.H.

    1991-01-01

    The pyrolysis of bitumen-impregnated sandstone produces three primary product streams: C{sub 1}-C{sub 4} hydrocarbons gases, a C{sub 5}{sup +} total liquid product, and a carbonaceous residue on the spent sand. The bitumen-derived hydrocarbon liquid was significantly upgraded relative to the native bitumen: it had a higher API gravity, lower Conradson carbon residue, asphaltene content, pour point and viscosity and a reduced distillation endpoint relative to the native bitumen. The elemental composition was little different from that of the native bitumen except for the hydrogen content which was lower. The bitumen-derived liquid produced in a 4-inch diameter fluidized-bed reactor from the Whiterocks tar sand deposit has been hydrotreated in a fixed-bed reactor to determine the extent of upgrading as a function of process operating variables. The extent of denitrogenation and desulfurization of the bitumen-derived liquid was used to monitor catalyst activity as a function of process operating variables and to estimate the extent of catalyst deactivation as a function of time on-stream. The apparent kinetics for the nitrogen and sulfur removal reactions were determined. Product distribution and yield data were also obtained.

  2. Comparison of two different multidimensional liquid-gas chromatography interfaces for determination of mineral oil saturated hydrocarbons in foodstuffs.

    PubMed

    Purcaro, Giorgia; Zoccali, Mariosimone; Tranchida, Peter Quinto; Barp, Laura; Moret, Sabrina; Conte, Lanfranco; Dugo, Paola; Mondello, Luigi

    2013-01-01

    This investigation focused on direct comparison of two popular multidimensional liquid-gas chromatography (LC-GC) systems, the Y-interface (retention gap approach) and the syringe-based interface (programmed temperature vaporizer approach). Such transfer devices are structurally very different, and could potentially have a substantial effect on the outcome of a specific application. In this work the application was a topic of much current interest, determination of mineral oil saturated hydrocarbon (MOSH) contamination of a series of food products (rice, pasta, icing sugar, olive oil); the final results were then compared. The two LC-GC methods developed were validated for linearity over the calibration range, analyte discrimination, precision, accuracy, and limits of detection and quantification. No significant differences were found between the two approaches.

  3. DETERMINATION OF SOLID-LIQUID EQUILIBRIA DATA FOR MIXTURES OF HEAVY HYDROCARBONS IN A LIGHT SOLVENT

    SciTech Connect

    F.V. Hanson; J.V. Fletcher; Karthik R.

    2003-06-01

    A methodology was developed using an FT-IR spectroscopic technique to obtain solid-liquid equilibria (SLE) data for mixtures of heavy hydrocarbons in significantly lighter hydrocarbon diluents. SLE was examined in multiple Model Oils that were assembled to simulate waxes. The various Model oils were comprised of C-30 to C-44 hydrocarbons in decane. The FT-IR technique was used to identify the wax precipitation temperature (WPT). The DSC technique was also used in the identification of the onset of the two-phase equilibrium in this work. An additional Model oil made up of C-20 to C-30 hydrocarbons in decane was studied using the DSC experiment. The weight percent solid below the WPT was calculated using the FT-IR experimental results. The WPT and the weight percent solid below the WPT were predicted using an activity coefficient based thermodynamic model. The FT-IR spectroscopy method is found to successfully provide SLE data and also has several advantages over other laboratory-based methods.

  4. Emission of polycyclic aromatic hydrocarbons from the pyrolysis of liquid crystal wastes.

    PubMed

    Chien, Yi-Chi; Liang, Ching-Ping; Shih, Pai-Haung

    2009-10-30

    A liquid crystal display can be described as a panel consisting of two plates of glass with liquid crystals in the space between. Generally, the liquid crystal wastes are extracted and separated into various fractions. Some recyclable materials, i.e., metals, glass, plastics, etc., are recycled, but the liquid crystals are incinerated. The emission factors for 16 U.S. EPA priority polycyclic aromatic hydrocarbons (PAHs) from the combustion of liquid crystal are approximately 390 and 1520 times higher than that of waste terephthalic acid and biological sludge combustion, respectively. In this study, we determined the emission of PAHs from the liquid crystals pyrolysis. We also investigated the fragments and gas compositions using on-line thermogravimetry-mass spectrometry (TG-MS). A temperature series of 14 fragments was analyzed in nitrogen, and was found to include m/z: 30, 32, 42, 44, 55, 57, 67, 81, 95, 109, 128, 166, 178, and 202. The fragments at m/z 32 represents formaldehyde and the fragment at m/z 44 is carbon dioxide. The fragments at m/z 55, 57, 67, 81, 95, and 109 represent hydrocarbon components, all of which may be liquid crystal by products. The TG-MS as analyzed above can offer a better understanding of the mechanisms of byproduct formation in liquid crystal waste pyrolysis. Experimentally, not detected (n.d.) -5.98 and n.d. -20.2 microg/g of 16 PAHs, in the particulate and gas phases, respectively, are determined from the emission of liquid crystal waste pyrolysis. The PAH profiles showed a predominance of naphthalene (42.6%) and phenanthrene (13.5%). The total PAH emissions for the 16 species were 7.75 and 44.05 microg/g in the particulate and gas phases, respectively, significantly lower than the values associated with liquid crystal combustion. From the viewpoint of PAH emission control, our results suggest that the pyrolysis is a better option for the disposal of liquid crystal wastes than that of combustion.

  5. Autothermal reforming of sulfur-free and sulfur-containing hydrocarbon liquids

    NASA Technical Reports Server (NTRS)

    1981-01-01

    The mechanisms by which various fuel component hydrocarbons related to both heavy petroleum and coal-derived liquids are converted to hydrogen without forming carbon were investigated. Reactive differences between paraffins and aromatics in autothermal reforming (ATR) were shown to be responsible for the observed fuel-specific carbon formation characteristics. The types of carbon formed in the reformer were identified by SEM and XRD analyses of catalyst samples and carbon deposits. From tests with both light and heavy paraffins and aromatics, it is concluded that high boiling point hydrocarbons and polynuclear aromatics enhance the propensity for carbon formation. The effects of propylene addition on the ATR performance of benzene are described. In ATR tests with mixtures of paraffins and aromatics, synergistic effects on conversion characteristics were identified. Indications that the sulfur content of the fuel may be the limiting factor for efficient ATR operation were found. The conversion and degradation effects of the sulfur additive (thiophene) were examined.

  6. Hydrocarbon group type determination in jet fuels by high performance liquid chromatography

    NASA Technical Reports Server (NTRS)

    Antoine, A. C.

    1977-01-01

    Results are given for the analysis of some jet and diesel fuel samples which were prepared from oil shale and coal syncrudes. Thirty-two samples of varying chemical composition and physical properties were obtained. Hydrocarbon types in these samples were determined by fluorescent indicator adsorption (FIA) analysis, and the results from three laboratories are presented and compared. Recently, rapid high performance liquid chromatography (HPLC) methods have been proposed for hydrocarbon group type analysis, with some suggestion for their use as a replacement of the FIA technique. Two of these methods were used to analyze some of the samples, and these results are also presented and compared. Two samples of petroleum-based Jet A fuel are similarly analyzed.

  7. CROWTM PROCESS APPLICATION FOR SITES CONTAMINATED WITH LIGHT NON-AQUEOUS PHASE LIQUIDS AND CHLORINATED HYDROCARBONS

    SciTech Connect

    L.A. Johnson, Jr.

    2003-06-30

    Western Research Institute (WRI) has successfully applied the CROWTM (Contained Recovery of Oily Wastes) process at two former manufactured gas plants (MGPs), and a large wood treatment site. The three CROW process applications have all occurred at sites contaminated with coal tars or fuel oil and pentachlorophenol (PCP) mixtures, which are generally denser than water and are classified as dense non-aqueous phase liquids (DNAPLs). While these types of sites are abundant, there are also many sites contaminated with gasoline, diesel fuel, or fuel oil, which are lighter than water and lie on top of an aquifer. A third site type occurs where chlorinated hydrocarbons have contaminated the aquifer. Unlike the DNAPLs found at MGP and wood treatment sites, chlorinated hydrocarbons are approximately one and a half times more dense than water and have fairly low viscosities. These contaminants tend to accumulate very rapidly at the bottom of an aquifer. Trichloroethylene (TCE) and perchloroethylene, or tetrachloroethylene (PCE), are the major industrial chlorinated solvents that have been found contaminating soils and aquifers. The objective of this program was to demonstrate the effectiveness of applying the CROW process to sites contaminated with light non-aqueous phase liquids (LNAPLs) and chlorinated hydrocarbons. Individual objectives were to determine a range of operating conditions necessary to optimize LNAPL and chlorinated hydrocarbon recovery, to conduct numerical simulations to match the laboratory experiments and determine field-scale recoveries, and determine if chemical addition will increase the process efficiency for LNAPLs. The testing consisted of twelve TCE tests; eight tests with PCE, diesel, and wood treatment waste; and four tests with a fuel oil-diesel blend. Testing was conducted with both vertical and horizontal orientations and with ambient to 211 F (99 C) water or steam. Residual saturations for the horizontal tests ranged from 23.6% PV to 0.3% PV

  8. Gas-liquid-liquid equilibria in mixtures of water, light gases, and hydrocarbons

    SciTech Connect

    Chao, K.C.

    1990-01-01

    Phase equilibrium in mixtures of water + light gases and water + heavy hydrocarbons has been investigated with the development of new local composition theory, new equations of state, and new experimental data. The preferential segregation and orientation of molecules due to different energies of molecular interaction has been simulated with square well molecules. Extensive simulation has been made for pure square well fluids and mixtures to find the local composition at wide ranges of states. A theory of local composition has been developed and an equation of state has been obtained for square well fluids. The new local composition theory has been embedded in several equations of state. The pressure of water is decoupled into a polar pressure and non-polar pressure according to the molecular model of water of Jorgensen et al. The polar pressure of water is combined with the BACK equation for the general description of polar fluids and their mixtures. Being derived from the steam table, the Augmented BACK equation is particularly suited for mixtures of water + non-polar substances such as the hydrocarbons. The hydrophobic character of the hydrocarbons had made their mixtures with water a special challenge. A new group contribution equation of state is developed to describe phase equilibrium and volumetric behavior of fluids while requiring only to know the molecular structure of the components. 15 refs., 1 fig.

  9. Diazido alkanes and diazido alkanols as combustion modifiers for liquid hydrocarbon ramjet fuels

    SciTech Connect

    Miller, R.S.

    1986-07-03

    This invention relates to liquid-hydrocarbon jet fuels and more particularly to azido additives to liquid-hydrocarbon ramjet fuels. In most liquid-fueled combustors such as the ramjet, the fuel is directly introduced into the upstream flow section of the combustion chamber in the form of sprays of droplets. These droplets subsequently mix with the external gas, heat up, gasify, combust, and thereby release heat to provide the propulsion energy. It is therefore obvious that the rates of gasification and mixing would closely affect the chemical heat release rate and, consequently, such important performance parameters as combustion efficiency and the tendency to exhibit combustion instability. Accordingly, and object of this invention is to provide a new, improved jet fuel and provide new additives for jet fuels. A further object of this invention is to provide a more-efficient jet fuel and reduce the ignition time for jet fuels. Still, a further object of this invention is to improve the mixing characteristics of the jet-fuel spray.

  10. Originating super-strong liquid crystalline polymers (SSLCPs). Final report

    SciTech Connect

    1994-12-31

    The work at the University of North Carolina at Chapel Hill focused on the experimental characterization of ring mobility in labeled polyaramides with deuterium Nuclear Magnetic Resonance (NMR). Los Alamos National Laboratory prepared the deuterium-labeled analogs of Super-Strong (SS), Liquid Crystalline Polymers (LCPs) and oligomers. These materials were studied to ascertain the influence of substituent size (at the diacid moiety) on the mobility of the labeled diamine. The results are currently being finalized for publication.

  11. Test program to provide confidence in liquid oxygen cooling of hydrocarbon fueled rocket thrust chambers

    NASA Technical Reports Server (NTRS)

    Armstrong, Elizabeth S.

    1986-01-01

    In previous tests of liquid oxygen cooling of hydrocarbon fueled rocket engines, small oxygen leaks developed at the throat of the thrust chamber and film cooled the hot gas side of the chamber wall without resulting in catastrophic failure. However, more testing is necessary to demonstrate that a catastropic failure would not occur if cracks developed further upstream between the injector and the throat, where the boundary layer has not been established. Since under normal conditions cracks are expected to form in the throat region of the thrust chamber, cracks must be initiated artificially in order to control their location. Several methods of crack initiation are discussed here.

  12. Diazido alkanes and diazido alkanols as combustion modifiers for liquid hydrocarbon ramjet fuels

    SciTech Connect

    Miller, R.S.; Moriarty, R.M.; Law, C.K.

    1988-05-03

    A liquid hydrocarbon ramjet fuel is described comprising from more than zero to 100 weight percent of a diazido alkanol of the general formula N/sub 3/CH/sub 2/(CH/sub 2/)/sub chi/CHOH(CH/sub 2/)/sub y/CH/sub 2/N/sub 3/ wherein chi is an integer of from 0 to 9, y is an integer of from 0 to 19, chi+y is an integer of from 0 to 19, and chiless than or equal toy, and the balance being a conventional jet fuel.

  13. Test program to provide confidence in liquid oxygen cooling of hydrocarbon fueled rocket thrust chambers

    NASA Technical Reports Server (NTRS)

    Armstrong, Elizabeth S.

    1986-01-01

    In previous tests of liquid oxygen cooling of hydrocarbon fueled rocket engines, small oxygen leaks developed at the throat of the thrust chamber and film cooled the hot gas side of the chamber wall without resulting in catastrophic failure. However, more testing is necessary to demonstrate that a catastropic failure would not occur if cracks developed further upstream between the injector and the throat, where the boundary layer has not been established. Since under normal conditions cracks are expected to form in the throat region of the thrust chamber, cracks must be initiated artificially in order to control their location. Several methods of crack initiation are discussed here.

  14. Fundamental and semi-global kinetic mechanisms for hydrocarbon combustion. Final report, March 1977-October 1980

    SciTech Connect

    Dryer, F L; Glassman, I; Brezinsky, K

    1981-03-01

    Over the past three and one half years, substantial research efforts of the Princeton Fuels Research Group have been directed towards the development of simplified mechanisms which would accurately describe the oxidation of hydrocarbons fuels. The objectives of this combustion research included the study of semi-empirical modeling (that is an overall description) of the chemical kinetic mechanisms of simple hydrocarbon fuels. Such fuels include the alkanes: ethane, propane, butane, hexane and octane as well as the critically important alkenes: ethene, propene and butene. As an extension to this work, the study of the detailed radical species characteristics of combustion systems was initiated as another major aspect of the program, with emphasis on the role of the OH and HO/sub 2/ radicals. Finally, the studies of important alternative fuel problems linked the program to longer range approaches to the energy supply question. Studies of alternative fuels composed the major elements of this area of the program. The efforts on methanol research were completed, and while the aromatics aspects of the DOE work have been a direct extension of efforts supported by the Air Force Office of Scientific Research, they represented a significant part of the overall research effort. The emphasis in the proposed program is to provide further fundamental understanding of the oxidation of hydrocarbon fuels which will be useful in guiding engineering approaches. Although the scope of program ranges from the fundamentals of chemical kinetics to that of alternative fuel combustion, the objective in mind is to provide insight and guidance to the understanding of practical combustion environments. The key to our approach has been our understanding of the fundamental combustion chemistry and its relation to the important practical combustion problems which exist in implementing energy efficient, alternate fuels technologies.

  15. Feasibility of liquid hydrocarbon fuels for SOFC with Ni-ScSZ anode

    NASA Astrophysics Data System (ADS)

    Kishimoto, Haruo; Yamaji, Katsuhiko; Horita, Teruhisa; Xiong, Yueping; Sakai, Natsuko; Brito, Manuel E.; Yokokawa, Harumi

    Solid oxide fuel cell (SOFC) operation with a nickel-scandia stabilized zirconia (Ni-ScSZ) cermet anode was carried out with liquid hydrocarbon of n-dodecane (C 12H 26), used as a model fuel of kerosene, without fuel dilution by inert carrier gas. Continuous operation was achieved for more than 120 h at S/C = 2.0 and at 800 °C. The obtained open circuit voltage was about -0.97 V and the average current density was about 140 mA cm -2 under the constant anode potential of -0.75 V versus air. This current density corresponded to fuel utilization of 55%. In the impedance spectra for the anode, two semicircles were observed not only for hydrogen but also for C1 to C12 paraffin. Electrode conductivity for each semicircle, σ H for high frequency part and σ L for low frequency part, were calculated by following equation: σ (S c m-2) = 1A/R where A (cm 2) is electrode area and R (Ω) is electrode resistance determined from each semicircle. Electrode conductivities for hydrocarbon fuels showed the same water partial pressure dependence as that for hydrogen whether fuel is diluted or not. Hydrogen produced by reforming reaction was the most active element for electrochemical oxidation at the anode even for hydrocarbon fuels.

  16. Stabilization of liquid hydrocarbon fuel combustion by using a programmable microwave discharge in a subsonic airflow

    SciTech Connect

    Kopyl, P. V.; Surkont, O. S.; Shibkov, V. M.; Shibkova, L. V.

    2012-06-15

    Under conditions of a programmable discharge (a surface microwave discharge combined with a dc discharge), plasma-enhanced combustion of alcohol injected into a subsonic (M = 0.3-0.9) airflow in the drop (spray) phase is stabilized. It is shown that the appearance of the discharge, its current-voltage characteristic, the emission spectrum, the total emission intensity, the heat flux, the electron density, the hydroxyl emission intensity, and the time dependences of the discharge current and especially discharge voltage change substantially during the transition from the airflow discharge to stabilized combustion of the liquid hydrocarbon fuel. After combustion stabilization, more than 80% of liquid alcohol can burn out, depending on the input power, and the flame temperature reaches {approx}2000 K.

  17. A correlation between surface, transport and thermo-elastic properties of liquid hydrocarbon: an experimental investigation

    NASA Astrophysics Data System (ADS)

    George, A. K.; Arafin, S.; Singh, R. N.; Carboni, C.

    2006-04-01

    The temperature dependence of surface tension and viscosity has been investigated in two multi-component liquid hydrocarbons, namely, crude oil samples with different API numbers. The surface tension is found to decrease linearly with temperature whereas viscosity exhibits Arrhenius type variation. These measured values along with the ultrasound velocity, density and the isothermal compressibility have been used to estimate a number of physical parameters such as the activation energy, attenuation factor and the shear wave velocity. Crude oil with larger API was found to have smaller activation energy. Shear velocity decreases exponentially with increasing temperature while the attenuation factor is found to increase linearly with temperature. The ratio of the surface tension to viscosity varies linearly as the square root of temperature. The product of the surface tension and the isothermal compressibility, often characterized as a fundamental or correlation length of the surface of the liquid, was found to yield a constant value for both samples.

  18. Microwave dielectric constant of liquid hydrocarbons: Application to the depth estimation of Titan's lakes

    NASA Astrophysics Data System (ADS)

    Paillou, Philippe; Mitchell, Karl; Wall, Stephen; Ruffié, Gilles; Wood, Charles; Lorenz, Ralph; Stofan, Ellen; Lunine, Jonathan; Lopes, Rosaly; Encrenaz, Pierre

    2008-03-01

    Cassini RADAR reveals the surface of Titan since flyby Ta acquired on October 2004. The RADAR instrument discovered volcanic structures, craters, dunes, channels, lakes and seas. In particular, flyby T16 realized in July 2006 imaged tens of radar-dark features close to Titan's north pole. They are interpreted as lakes filled with liquid hydrocarbons - mainly methane, a key material in the geologic and climatic history of Titan. In order to perform quantitative analysis and modeling of the radar response of Titan's lakes, the dielectric constant of liquid hydrocarbons is a crucial parameter, in particular to estimate the radar wave attenuation. We present here first measurements of the dielectric constant of LNG (Liquefied Natural Gas), mainly composed of methane, at Ku-band (10-13 GHz): we obtained a value $\\varepsilon$ = 1.75 - 0.002j. This value is used to model the radar backscattering of lakes observed during T16 flyby. Using a two-layer scattering model, we derive a relationship that is used to estimate a minimum depth for Titan's lakes. The proposed relationship is also coherent with the observation that the larger and then the deeper lakes are also the darker in radar images.

  19. REFORMING OF LIQUID HYDROCARBONS IN A NOVEL HYDROGEN-SELECTIVE MEMBRANE-BASED FUEL PROCESSOR

    SciTech Connect

    Shamsuddin Ilias

    2003-06-30

    We propose to develop an inorganic metal-metal composite membrane to study reforming of liquid hydrocarbons and methanol by equilibrium shift in membrane-reactor configuration, viewed as fuel processor. Based on our current understanding and experience in the Pd-ceramic composite membrane, we propose to further develop this membrane to a Pd and Pd-Ag alloy membrane on microporous stainless steel support to provide structural reliability from distortion due to thermal cycling. Because of the metal-metal composite structure, we believe that the associated end-seal problem in the Pd-ceramic composite membrane in tubular configuration would not be an issue at all. We plan to test this membrane as membrane-reactor-separator for reforming liquid hydrocarbons and methanol for simultaneous production and separation of high-purity hydrogen for PEM fuel cell applications. To improve the robustness of the membrane film and deep penetration into the pores, we have used osmotic pressure field in the electroless plating process. Using this novel method, we deposited thin Pd-film on the inside of microporous stainless steel tube and the deposited film appears to robust and defect free. Work is in progress to evaluate the hydrogen perm-selectivity of the Pd-stainless steel membrane.

  20. Magnetic ionic liquids as non-conventional extraction solvents for the determination of polycyclic aromatic hydrocarbons.

    PubMed

    Trujillo-Rodríguez, María J; Nacham, Omprakash; Clark, Kevin D; Pino, Verónica; Anderson, Jared L; Ayala, Juan H; Afonso, Ana M

    2016-08-31

    This work describes the applicability of magnetic ionic liquids (MILs) in the analytical determination of a group of heavy polycyclic aromatic hydrocarbons. Three different MILs, namely, benzyltrioctylammonium bromotrichloroferrate (III) (MIL A), methoxybenzyltrioctylammonium bromotrichloroferrate (III) (MIL B), and 1,12-di(3-benzylbenzimidazolium) dodecane bis[(trifluoromethyl)sulfonyl)]imide bromotrichloroferrate (III) (MIL C), were designed to exhibit hydrophobic properties, and their performance examined in a microextraction method for hydrophobic analytes. The magnet-assisted approach with these MILs was performed in combination with high performance liquid chromatography and fluorescence detection. The study of the extraction performance showed that MIL A was the most suitable solvent for the extraction of polycyclic aromatic hydrocarbons and under optimum conditions the fast extraction step required ∼20 μL of MIL A for 10 mL of aqueous sample, 24 mmol L(-1) NaOH, high ionic strength content of NaCl (25% (w/v)), 500 μL of acetone as dispersive solvent, and 5 min of vortex. The desorption step required the aid of an external magnetic field with a strong NdFeB magnet (the separation requires few seconds), two back-extraction steps for polycyclic aromatic hydrocarbons retained in the MIL droplet with n-hexane, evaporation and reconstitution with acetonitrile. The overall method presented limits of detection down to 5 ng L(-1), relative recoveries ranging from 91.5 to 119%, and inter-day reproducibility values (expressed as relative standard derivation) lower than 16.4% for a spiked level of 0.4 μg L(-1) (n = 9). The method was also applied for the analysis of real samples, including tap water, wastewater, and tea infusion.

  1. Influence of infrared final cooking on polycyclic aromatic hydrocarbon formation in ohmically pre-cooked beef meatballs.

    PubMed

    Kendirci, Perihan; Icier, Filiz; Kor, Gamze; Onogur, Tomris Altug

    2014-06-01

    Effects of infrared cooking on polycyclic aromatic hydrocarbon (PAH) formation in ohmically pre-cooked beef meatballs were investigated. Samples were pre-cooked in a specially designed-continuous type ohmic cooking at a voltage gradient of 15.26V/cm for 92s. Infrared cooking was applied as a final cooking method at different combinations of heat fluxes (3.706, 5.678, 8.475kW/m(2)), application distances (10.5, 13.5, 16.5cm) and application durations (4, 8, 12min). PAHs were analyzed by using high performance liquid chromatography (HPLC) equipped with a fluorescence detector. The total PAH levels were detected to be between 4.47 and 64μg/kg. Benzo[a] pyrene (B[a]P) and PAH4 (sum of B[a]P, chrysene (Chr), benzo[a]anthracene (B[a]A) and benzo[b]fluoranthene (B[b]F)) levels detected in meatballs were below the EC limits. Ohmic pre-cooking followed by infrared cooking may be regarded as a safe cooking procedure of meatballs from a PAH contamination point of view. Copyright © 2014 Elsevier Ltd. All rights reserved.

  2. Hydrocarbon liquid production via the bioCRACK process and catalytic hydroprocessing of the product oil

    DOE PAGES

    Schwaiger, Nickolaus; Elliott, Douglas C.; Ritzberger, Jurgen; ...

    2015-01-01

    Continuous hydroprocessing of liquid phase pyrolysis bio-oil, provided by BDI-BioEnergy International bioCRACK pilot plant at OMV Refinery in Schwechat/Vienna Austria was investigated. These hydroprocessing tests showed promising results using catalytic hydroprocessing strategies developed for unfractionated bio-oil. A sulfided base metal catalyst (CoMo on Al2O3) was evaluated. The bed of catalyst was operated at 400 °C in a continuous-flow reactor at a pressure of 12.1 MPa with flowing hydrogen. The condensed liquid products were analyzed and found that the hydrocarbon liquid was significantly hydrotreated so that nitrogen and sulfur were below the level of detection (<0.05), while the residual oxygen rangedmore » from 0.7 to 1.2%. The density of the products varied from 0.71 g/mL up to 0.79 g/mL with a correlated change of the hydrogen to carbon atomic ratio from 2.1 down to 1.9. The product quality remained high throughout the extended tests suggesting minimal loss of catalyst activity through the test. These tests provided the data needed to assess the quality of liquid fuel products obtained from the bioCRACK process as well as the activity of the catalyst for comparison with products obtained from hydrotreated fast pyrolysis bio-oils from fluidized-bed operation.« less

  3. Hydrocarbon liquid production via the bioCRACK process and catalytic hydroprocessing of the product oil

    SciTech Connect

    Schwaiger, Nickolaus; Elliott, Douglas C.; Ritzberger, Jurgen; Wang, Huamin; Pucher, Peter; Siebenhofer, Matthaus

    2015-01-01

    Continuous hydroprocessing of liquid phase pyrolysis bio-oil, provided by BDI-BioEnergy International bioCRACK pilot plant at OMV Refinery in Schwechat/Vienna Austria was investigated. These hydroprocessing tests showed promising results using catalytic hydroprocessing strategies developed for unfractionated bio-oil. A sulfided base metal catalyst (CoMo on Al2O3) was evaluated. The bed of catalyst was operated at 400 °C in a continuous-flow reactor at a pressure of 12.1 MPa with flowing hydrogen. The condensed liquid products were analyzed and found that the hydrocarbon liquid was significantly hydrotreated so that nitrogen and sulfur were below the level of detection (<0.05), while the residual oxygen ranged from 0.7 to 1.2%. The density of the products varied from 0.71 g/mL up to 0.79 g/mL with a correlated change of the hydrogen to carbon atomic ratio from 2.1 down to 1.9. The product quality remained high throughout the extended tests suggesting minimal loss of catalyst activity through the test. These tests provided the data needed to assess the quality of liquid fuel products obtained from the bioCRACK process as well as the activity of the catalyst for comparison with products obtained from hydrotreated fast pyrolysis bio-oils from fluidized-bed operation.

  4. Plasma Reforming of Liquid Hydrocarbon Fuels in Non-Thermal Plasma-Liquid Systems

    DTIC Science & Technology

    2010-04-30

    and advantageous of non- equilibrium chemically reacting plasmas. The main ideas are related to possibilities of cost-effective non-thermal plasma...properties of non- equilibrium plasma in heterogeneous gas-liquid systems; characteristics of plasma reforming of ethanol-water mixtures in plasma...thermodynamically equilibrium , has characteristics of high ionization by higher energetic density. This has merits of good rate of fuel decomposition but demerits

  5. Improvement of mineral oil saturated and aromatic hydrocarbons determination in edible oil by liquid-liquid-gas chromatography with dual detection.

    PubMed

    Zoccali, Mariosimone; Barp, Laura; Beccaria, Marco; Sciarrone, Danilo; Purcaro, Giorgia; Mondello, Luigi

    2016-02-01

    Mineral oils, which are mainly composed of saturated hydrocarbons and aromatic hydrocarbons, are widespread food contaminants. Liquid chromatography coupled to gas chromatography with flame ionization detection represents the method of choice to determine these two families. However, despite the high selectivity of this technique, the presence of olefins (particularly squalene and its isomers) in some samples as in olive oils, does not allow the correct quantification of the mineral oil aromatic hydrocarbons fraction, requiring additional off-line tools to eliminate them. In the present research, a novel on-line liquid chromatography coupled to gas chromatography method is described for the determination of hydrocarbon contamination in edible oils. Two different liquid chromatography columns, namely a silica one (to retain the bulk of the matrix) and a silver-ion one (which better retains the olefins), were coupled in series to obtain the mineral oil aromatic hydrocarbons hump free of interfering peaks. Furthermore, the use of a simultaneous dual detection, flame ionization detector and triple quadrupole mass spectrometer allowed us not only to quantify the mineral oil contamination, but also to evaluate the presence of specific markers (i.e. hopanes) to confirm the petrogenic origin of the contamination. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  6. Homogeneous liquid-liquid microextraction via flotation assistance for rapid and efficient determination of polycyclic aromatic hydrocarbons in water samples.

    PubMed

    Hosseini, Majid Haji; Rezaee, Mohammad; Akbarian, Saeid; Mizani, Farhang; Pourjavid, Mohammad Reza; Arabieh, Masoud

    2013-01-31

    In this work, a rapid, simple and efficient homogeneous liquid-liquid microextraction via flotation assistance (HLLME-FA) method was developed based on applying low density organic solvents without no centrifugation. For the first time, a special extraction cell was designed to facilitate collection of the low-density solvent extraction in the determination of four polycyclic aromatic hydrocarbons (PAHs) in water samples followed by gas chromatography-flame ionization detector (GC-FID). The effect of different variables on the extraction efficiency was studied simultaneously using experimental design. The variables of interest in the HLLME-FA were selected as extraction and homogeneous solvent volumes, ionic strength and extraction time. Response surface methodology (RSM) was applied to investigate the optimum conditions of all the variables. Using optimized variables in the extraction process, for all target PAHs, the detection limits, the precisions and the linearity of the method were found in the range of 14-41 μg L(-1), 3.7-10.3% (RSD, n=3) and 50-1000 μg L(-1), respectively. The proposed method has been successfully applied to the analysis of four target PAHs in the water samples, and satisfactory results were obtained.

  7. Determination of polycyclic aromatic hydrocarbons in soil samples using flotation-assisted homogeneous liquid-liquid microextraction.

    PubMed

    Hosseini, Majid Haji; Rezaee, Mohammad; Mashayekhi, Hossein Ali; Akbarian, Saeid; Mizani, Farhang; Pourjavid, Mohammad Reza

    2012-11-23

    In this study, flotation-assisted homogeneous liquid-liquid microextraction (FA-HLLME) was developed as a fast, simple, and efficient method for extraction of four polycyclic aromatic hydrocarbons (PAHs) in soil samples followed by gas chromatography-flame ionization detector (GC-FID) analysis. A special home-made extraction cell was designed to facilitate collection of the low-density extraction solvent without a need for centrifugation. In this method, PAHs were extracted from soil samples into methanol and water (1:1, v/v) using ultrasound in two steps followed by filtration as a clean-up step. The filtrate was added into the home-made extraction cell contained mixture of 1.0 mL methanol (homogenous solvent) and 150.0 μL toluene (extraction solvent). Using N(2) flotation, the dispersed extraction solvent was transferred to the surface of the mixture and was collected by means of a micro-syringe. Then, 2 μL of the collected organic solvent was injected into the GC-FID for subsequent analysis. Under optimal conditions, linearity of the method was in the range of 40-1000 μg kg(-1) soil (dry weight). The relative standard deviations in real samples varied from 5.9 to 15.2% (n=4). The proposed method was successfully applied to analyze the target PAHs in soil samples, and satisfactory results were obtained. Copyright © 2012 Elsevier B.V. All rights reserved.

  8. Solvent-impregnated agarose gel liquid phase microextraction of polycyclic aromatic hydrocarbons in water.

    PubMed

    Loh, Saw Hong; Sanagi, Mohd Marsin; Wan Ibrahim, Wan Aini; Hasan, Mohamed Noor

    2013-08-09

    A new microextraction procedure termed agarose gel liquid phase microextraction (AG-LPME) combined with gas chromatography-mass spectrometry (GC-MS) was developed for the determination of selected polycyclic aromatic hydrocarbons (PAHs) in water. The technique utilized an agarose gel disc impregnated with the acceptor phase (1-octanol). The extraction procedure was performed by allowing the solvent-impregnated agarose gel disc to tumble freely in the stirred sample solution. After extraction, the agarose gel disc was removed and subjected to centrifugation to disrupt its framework and to release the impregnated solvent, which was subsequently withdrawn and injected into the GC-MS for analysis. Under optimized extraction conditions, the new method offered high enrichment factors (89-177), trace level LODs (9-14ngL(-1)) and efficient extraction with good relative recoveries in the range of 93.3-108.2% for spiked drinking water samples. AG-LPME did not exhibit any problems related to solvent dissolution, and it provided high extraction efficiencies that were comparable to those of hollow fiber liquid phase microextraction (HF-LPME) and significantly higher than those of agarose film liquid phase microextraction (AF-LPME). This technique employed a microextraction format and utilized an environmentally compatible solvent holder that supported the green chemistry concept.

  9. Nonionic diethanolamide amphiphiles with isoprenoid-type hydrocarbon chains: thermotropic and lyotropic liquid crystalline phase behaviour

    SciTech Connect

    Sagnella, Sharon M.; Conn, Charlotte E.; Krodkiewska, Irena; Drummond, Calum J.

    2014-09-24

    The thermotropic and lyotropic liquid crystalline phase behaviour of a series of diethanolamide amphiphiles with isoprenoid-type hydrocarbon chains (geranoyl, H-farnesoyl, and phytanoyl) has been investigated. When neat, both H-farnesoyl and phytanoyl diethanolamide form a smectic liquid crystalline structure at sub-zero temperatures. In addition, all three diethanolamides exhibit a glass transition temperature at around -73 C. Geranoyl diethanolamide forms a lamellar crystalline phase with a lattice parameter of 17.4 {angstrom} following long term storage accompanied by the loss of the glass transition. In the presence of water, H-farnesoyl and phytanoyl diethanolamide form lyotropic liquid crystalline phases, whilst geranoyl diethanolamide forms an L{sub 2} phase. H-farnesoyl diethanolamide forms a fluid lamellar phase (L{sub {alpha}}) at room temperature and up to {approx} 40 C. Phytanoyl diethanolamide displays a rich mesomorphism forming the inverse diamond (Q{sub II}{sup D}) and gyroid (Q{sub II}{sup G}) bicontinuous cubic phases in addition to an L{sub {alpha}} phase.

  10. Flow measurement of liquid hydrocarbons with positive displacement meters: the correction for slippage

    NASA Astrophysics Data System (ADS)

    García-Berrocal, Agustín; Montalvo, Cristina; Blázquez, Juan; Balbás, Miguel

    2013-05-01

    In the oil industry, the economical and fiscal impact of the measurements accuracy on the custody transfer operations implies fulfilling strict requirements of legal metrology. In this work, we focus on the positive displacement meters (PD meters) for refined liquid hydrocarbons. The state of the art of the lack of accuracy due to slippage flow in these meters is revised. The slippage flow due to the pressure drop across the device has been calculated analytically by applying the Navier-Stokes equation. No friction with any wall of the slippage channel has been neglected and a more accurate formula than the one found in the literature has been obtained. PD meters are calibrated against a bidirectional prover in order to obtain their meter factor which allows correction of their indications. Instead of the analytical model, an empirical one is proposed to explain the variation of the meter factor of the PD meters with flow rate and temperature for a certain hydrocarbon. The empirical model is based on the historical calibration data, of 9 years on average, of 25 m with four types of refined hydrocarbon. This model has been statistically validated by linear least-squares fitting. By using the model parameters, we can obtain the meter factor corresponding to different conditions of temperature and flow rate from the conditions in which the devices were calibrated. The flow parameter is such that a 10% flow rate variation implies a meter factor variation lower than 0.01%. A rule of thumb value for the temperature parameter is 0.005% per degree Celsius. The model residuals allow surveillance of the device drift and quantifying its contribution to the meter factor uncertainty. The observed drift is 0.09% at 95% confidence level in the analyzed population of meters.

  11. Volatile liquid hydrocarbons in waters of the Gulf of Mexico and Caribbean Sea

    SciTech Connect

    Sauer, T.C. Jr.

    1980-03-01

    Concentrations of volatile liquid hydrocarbons (VLH), C/sub 6/-C/sub 14/ hydrocarbons, were determined in 1977 in coastal, shelf, and open-ocean surface waters of the Gulf of Mexico and Caribbean Sea. In open-ocean, nonpetroleum-polluted surface water, VLH concentrations were 60 ng.liter/sup -1/ while in heavily polluted Louisiana shelf and coastal water values reached 500 ng.liter/sup -1/. Caribbean surface samples had very low concentrations, 30 ng.liter/sup -1/. The relationship between anthropogenic gaseous hydrocarbons and VLH was approximately linear. Aromatic VLH accounted for 60 to 85% of the total VLH in surface waters. Cycloalkane concentrations were < 1.0 ng.liter/sup -1/ in open ocean water, 60 to 100 ng.liter/sup -1/ in polluted water (20% of total VLH). Alkanes were 15 ng.liter/sup -1/ in open ocean water, 40 ng.liter/sup -1/ in polluted water. The concentrations of five major VLH compounds (aromatics) in water samples - benzene, toluene, ethylbenzene, m/sup -/, p-xylenes, and o-xylene (called BTX) - were sufficient to predict the total VLH. The empirically determined relationship is VLH (ng.liter/sup -1/) = 1.42 BTX (ng.liter/sup -1/); r = 0.96. Subsurface VLH concentrations in samples of polluted waters collected from depths of 50 m were only 35 to 40 ng.liter/sup -1/ below surface concentrations. Open ocean subsurface samples had concentrations of only 30 ng.liter/sup -1/ at 30 to 50-m depths, comparable to those of Caribbean surface water.

  12. [Simultaneous determination of 15 polycyclic aromatic hydrocarbons additives in vegetable oil by ultra performance liquid chromatography].

    PubMed

    Dong, Guixian; Wang, Zhaoxia; Zhou, Xiaoge; Zhang, Xiaoyu; Wang, Ying; Zhang, Guifang

    2014-07-01

    To establish a rapid method for simultaneous determination of 15 polycyclic aromatic hydrocarbons (PAHs) in vegetable oil by ultra performance liquid chromatography with fluorescence detection. The vegetable oils were extracted with acetonitrile and acetone (1:1), purified with Oasis HLB and Sep-Pak Florsil column, separated on Waters PAH C18 (4.6 mm x 250 mm, 3 microm) special column for the analysis of polycyclic aromatic hydrocarbons with a mobile phase of acetonitrile, methanol and water for gradient elution, the column temperature was 35 degrees C, and the injection was 10 microl. The concentration of PAHs in samples were determined with fluorescence detector, and quantitative analysis was carried out by external standard. The 15 PAHs were completely separated within 9 min. Within 2 to 200 microg/L, the peak area and content was in a good linear relationship (r > or = 0.9990). The average recoveries of three spiked levels (10, 50 and 100 microg/kg) were 75.8% and 96.4%, with RSDs of 3.42% - 8.03% (n = 5). The limits of detection were 0.025 - 0.8 microg/kg and the limits of quantification were 0.08 - 3.0 microg/kg. This method is simple and quick with high sensitivity, and it is suitable for the determination of 15 PAHs in vegetable oil.

  13. Experiments on extinction of liquid hydrocarbon fires by a particulate mineral

    SciTech Connect

    Sharma, T.P.; Chimote, R.S.; Lal, B.B.; Singh, J. )

    1992-05-01

    This paper reports on a series of experiments on gasoline fires that were carried out in a 45-cm-high open-top mild steel tank in the diameter range of 27.5-75 cm in order to study experimentally how efficiently liquid hydrocarbon fires in storage tanks could be extinguished by a particulate mineral. For 30-, 45-, 60-, and 75-cm diameter tank fires, the minimum thickness of the fire extinction volume of the exfoliated vermiculite required for complete extinction of fires is 16 cm for an average 4.5-mm particle size distribution; further it is a linear tangent function of the minimum fire extinction volume of the exfoliated vermiculite and the size of fire to be extinguished.

  14. High-performance liquid chromatography and immunoassay techniques for monitoring urinary metabolites of polycyclic aromatic hydrocarbons

    SciTech Connect

    Chamberlain, V.C.

    1988-01-01

    The purpose of this research was to investigate the feasibility of using high performance liquid chromatography (HPLC) and enzyme linked immunosorbent assays (ELISA) as sensitive techniques for monitoring polycyclic aromatic hydrocarbon (PAH) metabolites in human urine. The method was tested using synthesized PAH conjugates as positive markers. Results showed that a PAH conjugate, S-(9,10-dihydro-9-hydroxy-10-phenanthryl)N-acetyl cysteine (PHONAC), present in HPLC effluent could be detected by ELISA at picomole levels, well below the sensitivity of the HPLC UV detector. Analyses of urine from mice dosed with phenanthrene demonstrated that a substance detected by HPLC which was not detected in ELISA tests was the principal phenanthrene metabolite. This substance was not hydrolysed by Beta-glucuronidase. PHONAC was detected by ELISA in mouse urine extracts subjected to HPLC.

  15. Pressurized liquid extraction of polycyclic aromatic hydrocarbons from silicone rubber passive samplers.

    PubMed

    Shahpoury, Pourya; Hageman, Kimberly J

    2013-11-01

    Silicone rubber passive samplers effectively concentrate organic contaminants from water and are simple-to-use and robust. However, during the extraction of analytes from the samplers with organic solvents, oligomers associated with the rubber are inevitably extracted and this creates analytic challenges. Additionally, extraction methods that use Soxhlet or shaking are time-consuming and use large volumes of solvent. We evaluated a new method for the extraction of polycyclic aromatic hydrocarbons from silicone rubber passive samplers that uses pressurized liquid extraction with gel permeation chromatography. Extraction with dichloromethane at 100°C provided better recoveries compared to that of 50°C. The recoveries of 14 individual PAHs ranged from 81% to 102% and the mean recovery was 93% (standard deviation=7). Relative to comparable methods in which Soxhlet or shaking were used for the extraction, this method uses considerably less solvent and time.

  16. Optimization of multiwalled carbon nanotubes reinforced hollow-fiber solid-liquid-phase microextraction for the determination of polycyclic aromatic hydrocarbons in environmental water samples using experimental design.

    PubMed

    Hamedi, Raheleh; Hadjmohammadi, Mohammad Reza

    2017-09-01

    A novel design of hollow-fiber liquid-phase microextraction containing multiwalled carbon nanotubes as a solid sorbent, which is immobilized in the pore and lumen of hollow fiber by the sol-gel technique, was developed for the pre-concentration and determination of polycyclic aromatic hydrocarbons in environmental water samples. The proposed method utilized both solid- and liquid-phase microextraction media. Parameters that affect the extraction of polycyclic aromatic hydrocarbons were optimized in two successive steps as follows. Firstly, a methodology based on a quarter factorial design was used to choose the significant variables. Then, these significant factors were optimized utilizing central composite design. Under the optimized condition (extraction time = 25 min, amount of multiwalled carbon nanotubes = 78 mg, sample volume = 8 mL, and desorption time = 5 min), the calibration curves showed high linearity (R(2)  = 0.99) in the range of 0.01-500 ng/mL and the limits of detection were in the range of 0.007-1.47 ng/mL. The obtained extraction recoveries for 10 ng/mL of polycyclic aromatic hydrocarbons standard solution were in the range of 85-92%. Replicating the experiment under these conditions five times gave relative standard deviations lower than 6%. Finally, the method was successfully applied for pre-concentration and determination of polycyclic aromatic hydrocarbons in environmental water samples. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  17. A study of hydrocarbons associated with brines from DOE geopressured wells. Final report

    SciTech Connect

    Keeley, D.F.

    1993-07-01

    Accomplishments are summarized on the following tasks: distribution coefficients and solubilities, DOE design well sampling, analysis of well samples, review of theoretical models of geopressured reservoir hydrocarbons, monitor for aliphatic hydrocarbons, development of a ph meter probe, DOE design well scrubber analysis, removal and disposition of gas scrubber equipment at Pleasant Bayou Well, and disposition of archived brines.

  18. Deoxygenation of waste cooking oil and non-edible oil for the production of liquid hydrocarbon biofuels.

    PubMed

    Romero, M J A; Pizzi, A; Toscano, G; Busca, G; Bosio, B; Arato, E

    2016-01-01

    Deoxygenation of waste cooking vegetable oil and Jatropha curcas oil under nitrogen atmosphere was performed in batch and semi-batch experiments using CaO and treated hydrotalcite (MG70) as catalysts at 400 °C. In batch conditions a single liquid fraction (with yields greater than 80 wt.%) was produced containing a high proportion of hydrocarbons (83%). In semi-batch conditions two liquid fractions (separated by a distillation step) were obtained: a light fraction and an intermediate fraction containing amounts of hydrocarbons between 72-80% and 85-88% respectively. In order to assess the possible use of the liquid products as alternative fuels a complete chemical characterization and measurement of their properties were carried out. Copyright © 2015 Elsevier Ltd. All rights reserved.

  19. 19 CFR 159.52 - Warehouse entry not liquidated until final withdrawal.

    Code of Federal Regulations, 2010 CFR

    2010-04-01

    ... 19 Customs Duties 2 2010-04-01 2010-04-01 false Warehouse entry not liquidated until final withdrawal. 159.52 Section 159.52 Customs Duties U.S. CUSTOMS AND BORDER PROTECTION, DEPARTMENT OF HOMELAND... Warehouse entry not liquidated until final withdrawal. Liquidation of a warehouse or rewarehouse entry...

  20. Laser deposition of diamond-like films from liquid aromatic hydrocarbons

    NASA Astrophysics Data System (ADS)

    Simakin, A. V.; Shafeev, G. A.; Loubnin, E. N.

    2000-02-01

    Diamond-like films are deposited on transparent substrates upon exposure of its interface with liquid hydrocarbons (toluene C 6H 5CH 3, benzene C 6H 6, and cumene C 6H 5CH(CH 3) 2) to pulsed visible laser radiation of a copper vapor laser ( λ=510.6 nm). The X-ray Auger electron spectroscopy (XAES), Reflection High Energy Electron Diffraction (RHEED), profilometry, and ellipsometry are employed to characterize the deposited films. The sp 3 fraction in the films amounts to 60%-70% and depends on the precursor. The addition of diamond nanoparticles to the liquid precursor results in their incorporation into the film. The average film thickness on a glass substrate increases with the number of laser shots and then saturates at about 100 nm. The films show excellent adherence and have microhardness of 50-70 GPa, as measured by nanoindentor. The effect of auto-regulation of the film thickness is discussed as the result of competition between ablation and deposition of the film.

  1. Steam reforming of liquid hydrocarbons over a nickel-alumina spinel catalyst

    NASA Astrophysics Data System (ADS)

    Fauteux-Lefebvre, Clémence; Abatzoglou, Nicolas; Blanchard, Jasmin; Gitzhofer, François

    Interest in steam reforming of liquid hydrocarbons is growing due to the necessity of developing reliable alternatives for their use in fuel cells. In particular, solid oxide fuel cells, which can operate with mixtures of H 2 and CO, are excellent candidates for being fed with liquid fuels coming from both fossil and renewable sources. Fossil-derived, synthetic diesel is an interesting option. In this work, an Al 2O 3-ZrO 2-supported nickel-alumina spinel was tested in a lab-scale isothermal packed-bed reactor as a catalyst of steam reforming of propane, hexadecane and tetralin as surrogates of constitutive families of all commercially available diesel fuels. The results show that the reaction reaches equilibrium at reaction severities lower than those reported in the literature. When operated at steam excess of 250%, carbon formation is not higher than expected by theoretical thermodynamic equilibrium calculations, and no significant catalyst deactivation is observed over the test durations. Scanning electron microscopy of the fresh and used catalyst surfaces shows no significant quantities of carbon.

  2. Test program to provide confidence in liquid oxygen cooling of hydrocarbon fueled rocket thrust chambers

    NASA Technical Reports Server (NTRS)

    Armstrong, E. S.

    1986-01-01

    An experimental program has been planned at the NASA Lewis Research Center to build confidence in the feasibility of liquid oxygen cooling for hydrocarbon fueled rocket engines. Although liquid oxygen cooling has previously been incorporated in test hardware, more runtime is necessary to gain confidence in this concept. In the previous tests, small oxygen leaks developed at the throat of the thrust chamber and film cooled the hot-gas side of the chamber wall without resulting in catastrophic failure. However, more testing is necessary to demonstrate that a catastrophic failure would not occur if cracks developed further upstream between the injector and the throat, where the boundary layer has not been established. Since under normal conditions cracks are expected to form in the throat region of the thrust chamber, cracks must be initiated artificially in order to control their location. Several methods of crack initiation are discussed in this report. Four thrust chambers, three with cracks and one without, should be tested. The axial location of the cracks should be varied parametrically. Each chamber should be instrumented to determine the effects of the cracks, as well as the overall performance and durability of the chambers.

  3. Ionic liquid coated magnetic nanoparticles for the gas chromatography/mass spectrometric determination of polycyclic aromatic hydrocarbons in waters.

    PubMed

    Galán-Cano, Francisco; Alcudia-León, María del Carmen; Lucena, Rafael; Cárdenas, Soledad; Valcárcel, Miguel

    2013-07-26

    In this paper, ionic liquid coated magnetic nanoparticles (IL-MNPs) have been prepared by covalent immobilization. The as-synthesized MNPs have been successfully used as sorbent for the extraction of polycyclic aromatic hydrocarbons (PAHs) from water samples, the analytes being finally determined by gas chromatography/mass spectrometry. The influence of several experimental variables (including the ionic strength, amount of MNPs, sample volume, agitation time and desorption solvent) has been considered in depth in the optimization process. The developed method, which has been analytically characterized under its optimal operation conditions, allows the detection of the analytes in the samples with method detection limits in the range from 0.04μgL(-1) (fluoranthene) to 1.11μgL(-1) (indeno(1,2,3-cd)pyrene). The repeatability of the method, expressed as relative standard deviation (RSD, n=7), varies between 4.0% (benzo[b]fluoranthene) and 8.9% (acenaphthene), while the enrichment factors are in the range from 49 (naphthalene) to 158 (fluoranthene). The proposed procedure has been applied for the determination of thirteen PAHs in water samples (tap, river, well and reservoir ones) with recoveries in the range from 75 to 102%.

  4. Valorization of Waste Lipids through Hydrothermal Catalytic Conversion to Liquid Hydrocarbon Fuels with in Situ Hydrogen Production

    SciTech Connect

    Kim, Dongwook; Vardon, Derek R.; Murali, Dheeptha; Sharma, Brajendra K.; Strathmann, Timothy J.

    2016-03-07

    We demonstrate hydrothermal (300 degrees C, 10 MPa) catalytic conversion of real waste lipids (e.g., waste vegetable oil, sewer trap grease) to liquid hydrocarbon fuels without net need for external chemical inputs (e.g., H2 gas, methanol). A supported bimetallic catalyst (Pt-Re/C; 5 wt % of each metal) previously shown to catalyze both aqueous phase reforming of glycerol (a triacylglyceride lipid hydrolysis coproduct) to H2 gas and conversion of oleic and stearic acid, model unsaturated and saturated fatty acids, to linear alkanes was applied to process real waste lipid feedstocks in water. For reactions conducted with an initially inert headspace gas (N2), waste vegetable oil (WVO) was fully converted into linear hydrocarbons (C15-C17) and other hydrolyzed byproducts within 4.5 h, and H2 gas production was observed. Addition of H2 to the initial reactor headspace accelerated conversion, but net H2 production was still observed, in agreement with results obtained for aqueous mixtures containing model fatty acids and glycerol. Conversion to liquid hydrocarbons with net H2 production was also observed for a range of other waste lipid feedstocks (animal fat residuals, sewer trap grease, dry distiller's grain oil, coffee oil residual). These findings demonstrate potential for valorization of waste lipids through conversion to hydrocarbons that are more compatible with current petroleum-based liquid fuels than the biodiesel and biogas products of conventional waste lipid processing technologies.

  5. Liquid effluent retention facility final-status groundwater monitoring plan

    SciTech Connect

    Sweeney, M.D.; Chou, C.J.; Bjornstad, B.N.

    1997-09-01

    The following sections describe the groundwater-monitoring program for the Liquid Effluent Retention Facility (LERF). The LERF is regulated under the Resource Conservation and Recovery Act of 1976 (RCRA). The LERF is included in the {open_quotes}Dangerous Waste Portion of the Resource Conservation and Recovery Act Permit for the Treatment, Storage, and Disposal of Dangerous Waste, Permit WA890008967{close_quotes}, (referred to herein as the Permit) (Ecology 1994) and is subject to final-status requirements for groundwater monitoring (WAC 173-303-645). This document describes a RCRA/WAC groundwater detection-monitoring program for groundwater in the uppermost aquifer system at the LERF. This plan describes the LERF monitoring network, constituent list, sampling schedule, statistical methods, and sampling and analysis protocols that will be employed for the LERF. This plan will be used to meet the groundwater monitoring requirements from the time the LERF becomes part of the Permit and through the post-closure care period, until certification of final closure.

  6. Influence of liquid water and soil temperature on petroleum hydrocarbon toxicity in Antarctic soil.

    PubMed

    Schafer, Alexis N; Snape, Ian; Siciliano, Steven D

    2009-07-01

    Fuel spills in Antarctica typically occur in rare ice-free oases along the coast, which are areas of extreme seasonal freezing. Spills often occur at subzero temperatures, but little is known of ecosystem sensitivity to pollutants, in particular the influence that soil liquid water and low temperature have on toxicity of petroleum hydrocarbons (PHC) in Antarctic soil. To evaluate PHC toxicity, 32 locations at an aged diesel spill site in Antarctica were sampled nine times to encompass frozen, thaw, and refreeze periods. Toxicity was assessed using potential activities of substrate-induced respiration, basal respiration, nitrification, denitrification, and metabolic quotient as well as microbial community composition and bacterial biomass. The most sensitive indicator was community composition with a PHC concentration effecting 25% of the population (EC25) of 800 mg/kg, followed by nitrification (2,000 mg/kg), microbial biomass (2,400 mg/kg), and soil respiration (3,500 mg/kg). Despite changes in potential microbial activities and composition over the frozen, thaw, and refreeze period, the sensitivity of these endpoints to PHC did not change with liquid water or temperature. However, the variability associated with ecotoxicity data increased at low liquid water contents. As a consequence of this variability, highly replicated (n = 50) experiments are needed to quantify a 25% ecological impairment by PHCs in Antarctic soils at a 95% level of significance. Increases in biomass and respiration associated with changes in community composition suggest that PHC contamination in Antarctic soils may have irrevocable effects on the ecosystem.

  7. Liquid fuels production from biomass. Final report, for period ending June 30, 1980

    SciTech Connect

    Levy, P. F.; Sanderson, J. E.; Ashare, E.; Wise, D. L.; Molyneaux, M. S.

    1980-01-01

    The current program to convert biomass into liquid hydrocarbon fuels is an extension of a previous program to ferment marine algae to acetic acid. In that study it was found that marine algae could be converted to higher aliphatic organic acids and that these acids could be readily removed from the fermentation broth by membrane or liquid-liquid extraction. It was then proposed to convert these higher organic acids via Kolbe electrolysis to aliphatic hydrocarbons, which may be used as a diesel fuel. The specific goals for the current program are: (1) establish conditions under which substrates other than marine algae may be converted in good yield to organic acids, here the primary task is methane suppression; (2) modify the current 300-liter fixed packed bed batch fermenter to operate in a continuous mode; (3) change from membrane extraction of organic acids to liquid-liquid extraction; (4) optimize the energy balance of the electrolytic oxidation process, the primary task is to reduce the working potential required for the electrolysis while maintaining an adequate current density; (5) scale the entire process up to match the output of the 300 liter fermenter; and (6) design pilot plant and commercial size plant (1000 tons/day) processes for converting biomass to liquid hydrocarbon fuels and perform an economic analysis for the 1000 ton/day design.

  8. Macrocyclic polyamine-functionalized silica as a solid-phase extraction material coupled with ionic liquid dispersive liquid-liquid extraction for the enrichment of polycyclic aromatic hydrocarbons.

    PubMed

    Liu, Longhui; He, Lijun; Jiang, Xiuming; Zhao, Wenjie; Xiang, Guoqiang; Anderson, Jared L

    2014-04-01

    In this study, silica modified with a 30-membered macrocyclic polyamine was synthesized and first used as an adsorbent material in SPE. The SPE was further combined with ionic liquid (IL) dispersive liquid-liquid microextraction (DLLME). Five polycyclic aromatic hydrocarbons were employed as model analytes to evaluate the extraction procedure and were determined by HPLC combined with UV/Vis detection. Acetone was used as the elution solvent in SPE as well as the dispersive solvent in DLLME. The enrichment of analytes was achieved using the 1,3-dibutylimidazolium bis[(trifluoromethyl)sulfonyl]imide IL/acetone/water system. Experimental conditions for the overall macrocycle-SPE-IL-DLLME method, such as the amount of adsorbent, sample solution volume, sample solution pH, type of elution solvent as well as addition of salt, were studied and optimized. The developed method could be successfully applied to the analysis of four real water samples. The macrocyclic polyamine offered higher extraction efficiency for analytes compared with commercially available C18 cartridge, and the developed method provided higher enrichment factors (2768-5409) for model analytes compared with the single DLLME. Good linearity with the correlation coefficients ranging from 0.9983 to 0.9999 and LODs as low as 0.002 μg/L were obtained in the proposed method.

  9. Dispersion-solidification liquid-liquid microextraction for volatile aromatic hydrocarbons determination: comparison with liquid phase microextraction based on the solidification of a floating drop.

    PubMed

    Vickackaite, Vida; Pusvaskiene, Edita

    2009-10-01

    Two microextraction techniques--liquid phase microextraction based on solidification of a floating organic drop (LPME-SFO) and dispersive liquid-liquid microextraction combined with a solidification of a floating organic drop (DLLME-SFO)--are explored for benzene, toluene, ethylbenzene and o-xylene sampling and preconcentration. The investigation covers the effects of extraction solvent type, extraction and disperser solvents' volume, and the extraction time. For both techniques 1-undecanol containing n-heptane as internal standard was used as an extracting solvent. For DLLME-SFO acetone was used as a disperser solvent. The calibration curves for both techniques and for all the analytes were linear up to 10 microg/mL, correlation coefficients were in the range 0.997-0.998, enrichment factors were from 87 for benzene to 290 for o-xylene, detection limits were from 0.31 and 0.35 microg/L for benzene to 0.15 and 0.10 microg/L for o-xylene for LPME-SFO and DLLME-SFO, respectively. Repeatabilities of the results were acceptable with RSDs up to 12%. Being comparable with LPME-SFO in the analytical characteristics, DLLME-SFO is superior to LPME-SFO in the extraction time. A possibility to apply the proposed techniques for volatile aromatic hydrocarbons determination in tap water and snow was demonstrated.

  10. 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.

  11. Determination of descriptors for polycyclic aromatic hydrocarbons and related compounds by chromatographic methods and liquid-liquid partition in totally organic biphasic systems.

    PubMed

    Ariyasena, Thiloka C; Poole, Colin F

    2014-09-26

    Retention factors on several columns and at various temperatures using gas chromatography and from reversed-phase liquid chromatography on a SunFire C18 column with various mobile phase compositions containing acetonitrile, methanol and tetrahydrofuran as strength adjusting solvents are combined with liquid-liquid partition coefficients in totally organic biphasic systems to calculate descriptors for 23 polycyclic aromatic hydrocarbons and eighteen related compounds of environmental interest. The use of a consistent protocol for the above measurements provides descriptors that are more self consistent for the estimation of physicochemical properties (octanol-water, air-octanol, air-water, aqueous solubility, and subcooled liquid vapor pressure). The descriptor in this report tend to have smaller values for the L and E descriptors and random differences in the B and S descriptors compared with literature sources. A simple atom fragment constant model is proposed for the estimation of descriptors from structure for polycyclic aromatic hydrocarbons. The new descriptors show no bias in the prediction of the air-water partition coefficient for polycyclic aromatic hydrocarbons unlike the literature values. Copyright © 2014 Elsevier B.V. All rights reserved.

  12. Changes in liquid water alter nutrient bioavailability and gas diffusion in frozen antarctic soils contaminated with petroleum hydrocarbons.

    PubMed

    Harvey, Alexis Nadine; Snape, Ian; Siciliano, Steven Douglas

    2012-02-01

    Bioremediation has been used to remediate petroleum hydrocarbon (PHC)-contaminated sites in polar regions; however, limited knowledge exists in understanding how frozen conditions influence factors that regulate microbial activity. We hypothesized that increased liquid water (θ(liquid) ) would affect nutrient supply rates (NSR) and gas diffusion under frozen conditions. If true, management practices that increase θ(liquid) should also increase bioremediation in polar soils by reducing nutrient and oxygen limitations. Influence of θ(liquid) on NSR was determined using diesel-contaminated soil (0-8,000 mg kg(-1)) from Casey Station, Antarctica. The θ(liquid) was altered between 0.007 and 0.035 cm(3) cm(-3) by packing soil cores at different bulk densities. The nutrient supply rate of NH 4+ and NO 3-, as well as gas diffusion coefficient, D(s), were measured at two temperatures, 21°C and -5°C, to correct for bulk density effects. Freezing decreased NSR of both NH 4+ and NO 3-, with θ(liquid) linked to nitrate and ammonia NSR in frozen soil. Similarly for D(s), decreases due to freezing were much more pronounced in soils with low θ(liquid) compared to soils with higher θ(liquid) contents. Additional studies are needed to determine the relationship between degradation rates and θ(liquid) under frozen conditions. Copyright © 2011 SETAC.

  13. Determination of polynuclear aromatic hydrocarbons in seafood by liquid chromatography with fluorescence detection

    SciTech Connect

    Perfetti, G.A.; Nyman, P.J.; Fisher, S.; Joe, F.L. Jr.; Diachenko, G.W.

    1992-09-01

    Modification of a previously published method for determination of polynuclear aromatic hydrocarbons (PAHs) produces very clean seafood extracts in less than half the time. After alkaline digestion of the seafood, PAHs were partitioned into 1,2,3-trichlorotrifluoroethane. The resulting extract was cleaned up by solid-phase extraction on alumina, silica, and C{sub 18} adsorbents and then analyzed by gradient reversed-phase liquid chromatography with programmable fluorescence detection. Average recoveries of 12 PAHs [acenaphthene, anthracene, fluoranthene, pyrene, benz(a)anthracene, chrysene, benzo(b)fluoranthene, benzo(k)-fluoranthene, benzo(k)-fluoranthene, benzo(a)pyrene, dibenz(a,h)anthracene, benzo(ghi)perylene, and indeno(1,2,3-cd)pyrene] from 5 different matrixes (mussels, oysters, clams, crabmeat, and salmon)spiked at low parts-per-billion levels ranged from 76 to 94%. Estimated limits of quantitation ranged from 0.01 to 0.6 ppb PAHs in extracts that were free of matrix interferences. Results of analyses of a mussels standard reference material obtained from the National Institute of Standards and Technology were in good agreement with the certified values. 16 refs., 3 figs., 4 tabs.

  14. Determination of polycyclic aromatic hydrocarbons in marine samples by high-performance liquid chromatography

    SciTech Connect

    Obana, H.; Hori, S.; Kashimoto, T.

    1981-05-01

    It has been reported that polycyclic aromatic hydrocarbons (PAHs) are widely distributed in the environment, although their concentrations are quite low. Some PAHs, benzo(a)pyrene, dibenz(a,h)anthracene and 3-methycholanthrene, are carcinogenic to mammals after in vivo hydroxylation by mixed function oxidases. PAHs originate largely from smoke, soot, and exhaust gas produced by combustion and from petroleum oil spilled into the sea, so that the quantity of PAHs in the environment is broadly related to the level of contamination in a given region. Although PAHs have been determined by a TLC-fluorescence method, these methods suffer from complex pretreatment. On the other hand, the development of high-performance liquid chromatography (HPLC) has made it possible to analyze PAHs with good separation and high sensitivity and to simplify the pretreatment processes. In this study, ten PAHs in sediments, oyster, and wakame seaweed were determined by HPLC with a fluorescence detector (HPLC-FD). The contents and the patterns of PAHs found in sediments and marine samples may be used as an indicator of petroleum contamination in the sea.

  15. Emission of polycyclic aromatic hydrocarbons (PAHs) from the liquid injection incineration of petrochemical industrial wastewater.

    PubMed

    Wang, Lin-Chi; Wang, I-Ching; Chang, Juu-En; Lai, Soon-Onn; Chang-Chien, Guo-Ping

    2007-09-05

    This study investigated the emission of polycyclic aromatic hydrocarbons (PAHs) from stack flue gas and air pollution control device (APCD) effluent of the liquid injection incinerator (LII) disposing the petrochemical industrial wastewater, and PAH removal efficiencies of wet electrostatic precipitator (WESP) and wet scrubber (WSB). The PAH carcinogenic potency were investigated with the benzo(a)pyrene equivalent concentration (BaP(eq)). The remarkably high total-BaP(eq) concentration (220 microgNm(-3)) in the stack flue gas was much higher than those of several published emission sources, and indicated the possible influence on its surrounding environment. The total-PAH emission factors of the WESP, WSB and stack flue gas were 78.9, 95.7 and 30,900 microgL(-1) wastewater, respectively. The removal efficiencies of total-PAHs were 0.254, 0.309 and 0.563% for WESP, WSB and overall, respectively, suggesting that the use of both WESP and WSB shows insignificant PAH removal efficiencies, and 99.4% of total-PAHs was directly emitted to the ambient air through the stack flue gas. This finding suggested that the better incineration efficiencies, and APCD removal efficiencies for disposing the petrochemical industrial wastewater are necessary in future.

  16. Waste polypropylene plastic conversion into liquid hydrocarbon fuel for producing electricity and energies.

    PubMed

    Sarker, Moinuddin; Rashid, Mohammad Mamunor; Molla, Mohammad

    2012-12-01

    Thermal degradation of polypropylene (PP) waste plastic is batched process studied for the purpose of converting waste PP into liquid hydrocarbon fuel and useful chemicals. The stainless steel reactor is used for conversion to fuel; this reactor chamber has a diameter of 6 inches, height of 18 inches and a temperature input capacity of 500 degrees C. The temperature of 150-370 degrees C was used for PP conversion into fuel. We have also used 1 kg PP waste plastic for conversion into fuel and HZSM-5 catalyst of 5% by preference was used by total weight of sample. Yield percentages obtained from PP to fuel are 92%, 2% light gas and 6% residue. Experimental finish time was 5.25 hours. By gas chromatograph/mass spectrometry instrumental analysis, the PP to fuel carbon range is found to be C3-C25,and the low sulfur level is detected by the American Society for Testing and Materials (ASTM) test method to be <1.0 ppm.

  17. Supra-Atomic Coarse-Grained GROMOS Force Field for Aliphatic Hydrocarbons in the Liquid Phase.

    PubMed

    Eichenberger, Andreas P; Huang, Wei; Riniker, Sereina; van Gunsteren, Wilfred F

    2015-07-14

    A supra-atomic coarse-grained (CG) force field for liquid n-alkanes is presented. The model was calibrated using experimental thermodynamic data and structural as well as energetic properties for 14 n-alkanes as obtained from atomistic fine-grained (FG) simulations of the corresponding hydrocarbons using the GROMOS 45A3 biomolecular force field. A variation of the nonbonded force-field parameters obtained from mapping the FG interactions onto the CG degrees of freedom to fit the density and heat of vaporization to experimental values turned out to be mandatory for a correct reproduction of these data by the CG model, while the bonded force-field parameters for the CG model could be obtained from a Boltzmann-weighted fit with some variations with respect to the corresponding properties from the FG simulations mapped onto the CG degrees of freedom. The model presents 6 different CG bead types, for bead sizes from 2 to 4 distinguishing between terminal and nonterminal beads within an alkane chain (end or middle). It contains different nonbonded Lennard-Jones parameters for the interaction of CG alkanes with CG water. The CG alkane model was further tested by comparing predictions of the excess free energy, the self-diffusion constant, surface tension, isothermal compressibility, heat capacity, thermal expansion coefficient, and shear viscosity for n-alkanes to experimental values. The CG model offers a thermodynamically calibrated basis for the development of CG models of lipids.

  18. Inhibition of natural gas hydrates in the presence of liquid hydrocarbons forming structure H.

    PubMed

    Seo, Yutaek; Kang, Seong-Pil; Jang, Wonho; Kim, Seonwook

    2010-05-13

    The effects of LMGS (large molecule guest substance) amount on the thermodynamics of natural gas hydrates, as well as structural characteristics of mixed hydrates of LMGS and natural gas, have been studied. The addition of 1.7 wt % neohexane (NH) to water induced inhibition of natural gas hydrates, and this inhibition effect increased with increased addition of NH up to 7.8 wt %. However, the hydrate equilibrium condition changed slightly when the concentration of NH further increased from 7.8 to 14.5 wt %. Investigations on structural characteristics were carried out by analyzing (13)C NMR spectra of mixed hydrates formed from the mixture of natural gas and NH. They indicate that two hydrate structures of II and H coexist simultaneously, and the ratio of structure H to II decreased from 0.97 to 0.43 when the NH concentration decreased from 14.5 to 7.8 wt %. In addition, it was confirmed that ethane, propane, and iso-butane gas molecules do not participate in the formation of structure H and only enclathrated in large cages of structure II. These results indicate the existence of multiple hydrate structures, which must be considered in many industrial applications when mixed hydrates are formed from multicomponent gas mixtures and liquid hydrocarbons.

  19. Effect of interface fertilization on biodegradation of polycyclic aromatic hydrocarbons present in nonaqueous-phase liquids.

    PubMed

    Tejeda-Agredano, M C; Gallego, S; Niqui-Arroyo, J L; Vila, J; Grifoll, M; Ortega-Calvo, J J

    2011-02-01

    The main goal of this study was to use an oleophilic biostimulant (S-200) to target possible nutritional limitations for biodegradation of polycyclic aromatic hydrocarbons (PAHs) at the interface between nonaqueous-phase liquids (NAPLs) and the water phase. Biodegradation of PAHs present in fuel-containing NAPLs was slow and followed zero-order kinetics, indicating bioavailability restrictions. The biostimulant enhanced the biodegradation, producing logistic (S-shaped) kinetics and 10-fold increases in the rate of mineralization of phenanthrene, fluoranthene, and pyrene. Chemical analysis of residual fuel oil also evidenced an enhanced biodegradation of the alkyl-PAHs and n-alkanes. The enhancement was not the result of an increase in the rate of partitioning of PAHs into the aqueous phase, nor was it caused by the compensation of any nutritional deficiency in the medium. We suggest that biodegradation of PAH by bacteria attached to NAPLs can be limited by nutrient availability due to the simultaneous consumption of NAPL components, but this limitation can be overcome by interface fertilization.

  20. Biodegradation of polycyclic aromatic hydrocarbons in a two-liquid-phase system

    SciTech Connect

    Vanneck, P.; Beeckman, M.; Saeyer, N. De; Verstraete, W.; D`Haene, S.

    1995-12-31

    The use of a two-liquid-phase system consisting of silicone oil and water for biodegrading polycyclic aromatic hydrocarbons (PAHs) was investigated. Biomass determinations indicated that the cells were mainly growing at the silicon oil-water interface. In shaken and aerated systems with PAHs and inoculum, 97% and 80%, respectively, of the total biomass was attached to the silicone phase. PAH concentrations in the silicon phase dropped by a factor 2 to 100 when microorganisms were present. Biodegradation rates in these systems varied from 3.6 to 5 mg PAH-C/L reactor{center_dot}d. In the shaken systems at 28 C, the measured CO{sub 2} production rate was equal to 9.1 mg CO{sub 2}/L reactor{center_dot}d and corresponded to a 50% conversion to CO{sub 2}. In the aerated systems at 10 C, however, only 25% of the PAH-C was converted to CO{sub 2}, resulting in a CO{sub 2} production rate of 0.5 mg CO{sub 2}/L reactor{center_dot}d.

  1. The Application of High-Performance Liquid Chromatography to the Analysis of Petroleum Materials. Part 2. Quantitative Hydrocarbon-Type Analysis.

    DTIC Science & Technology

    Quantitative hydrocarbon type analysis of middle distillate petroleum products, with emphasis on straight-run (olefin-free) diesel fuels has been accomplished by high performance liquid chromatography using silica gel absorbents.

  2. Ambient hydrocarbon and ozone concentrations near a refinery, Benicia, California, 1975. Final report

    SciTech Connect

    Sexton, K.; Westberg, H.

    1980-02-01

    As part of an effort to characterize airborne emissions from petroleum refineries, an ambient air monitoring study was conducted near the Exxon refinery at Benicia, California, during September 8-22, 1975. Ground-level sampling facilities and an airplane equipped with air pollutant monitoring instruments provided an integrated, three dimensional monitoring network. Measurements included ozone, oxides of nitrogen, methane, carbon monoxide, individual C2-C6 hydrocarbons, halocarbons, condensation. Increased concentrations of hydrocarbons, carbon monoxide, condensation nuclei and nitrogen oxides, as well as decreased ozone levels were observed less than five miles from the refinery. At distances greater than 5 miles, elevated condensation nuclei and hydrocarbons were still observed but no discernible differences from background could be detected in NOx, O3, and CO.

  3. Solubility of aliphatic hydrocarbons in piperidinium ionic liquids: measurements and modeling in terms of perturbed-chain statistical associating fluid theory and nonrandom hydrogen-bonding theory.

    PubMed

    Paduszyński, Kamil; Domańska, Urszula

    2011-11-03

    Ionic liquids (ILs) reveal many unique properties which make them very interesting for applications in modern "green" technologies. For that reason, detailed knowledge about correlations between the ions' structure, their combinations, and the bulk properties is of great importance. That knowledge can be accessed by reliable measurements and modeling of systems with ILs in terms of various theoretical approaches. In this paper we report new experimental results on liquid-liquid equilibrium (LLE) measurements of 10 binary systems composed of piperidinium ILs [namely, 1-propyl-1-methylpiperidinium bis(trifluoromethylsulfonyl)imide and 1-butyl-1-methylpiperidinium bis(trifluoromethylsulfonyl)imide] and aliphatic hydrocarbons (n-hexane, n-heptane, n-octane, cyclohexane, and cycloheptane). Moreover, new results on liquid density of pure 1-butyl-1-methylpiperidinium bis(trifluoromethylsulfonyl)imide are presented. Upper critical solution temperature type of phase behavior for all studied systems was observed. Decrease of solubility of n-alkane with an increase of its alkyl chain length and increase of solubility when changing linear into cyclic structure of hydrocarbon were detected. LLE modeling of investigated systems was performed in terms of two modern theories, namely, perturbed-chain statistical associating fluid theory (PC-SAFT) and nonrandom hydrogen-bonding theory (NRHB). Pure fluid parameters of the models were obtained from fitting of experimental liquid density and solubility parameter data at ambient pressure and tested against high pressure densities. Then literature values of activity coefficients of n-alkanes and cycloalkanes at infinitely diluted mixtures with ILs were used to optimize binary interaction parameters of the models. Finally, the LLE phase diagrams were calculated with average absolute relative deviations of 4.1% and 3.4% of the IL mole fraction for PC-SAFT and NRHB, respectively. The PC-SAFT and NRHB models were both able to capture phase

  4. Accurate measure by weight of liquids in industry. Final report

    SciTech Connect

    Muller, M.R.

    1992-12-12

    This research`s focus was to build a prototype of a computerized liquid dispensing system. This liquid metering system is based on the concept of altering the representative volume to account for temperature changes in the liquid to be dispensed. This is actualized by using a measuring tank and a temperature compensating displacement plunger. By constantly monitoring the temperature of the liquid, the plunger can be used to increase or decrease the specified volume to more accurately dispense liquid with a specified mass. In order to put the device being developed into proper engineering perspective, an extensive literature review was undertaken on all areas of industrial metering of liquids with an emphasis on gravimetric methods.

  5. Distribution and composition of polycyclic aromatic hydrocarbons within experimental microcosms treated with liquid creosote

    SciTech Connect

    Bestari, K.T.J.; Solomon, K.R.; Steele, T.S.; Sibley, P.K.; Robinson, R.D.; Day, K.E.

    1998-12-01

    Temporal changes in the distribution and relative composition of 15 priority polycyclic aromatic hydrocarbons (PAHs) in water, sediment, and absorbed to polyvinylchloride (PVC) strips were assessed following direct application of liquid creosote to aquatic microcosms. Fourteen microcosms were treated with nominal creosote concentrations ranging from 0.06 to 109 mg/L and two microcosms served as controls. Quantitative analysis of PAHs was performed using high-performance liquid chromatography equipped with a fluorescence detector. Post-treatment concentration of PAHs in water decreased exponentially with time. At 2 d posttreatment, total PAHs ({Sigma} PAH) ranged from 7.3 {micro}g/L to 5,803.2 {micro}g/L; by 84 d, {Sigma} PAH in the same microcosms was reduced to between 0.8 {micro}g/L and 13.9 {micro}g/L, respectively. The relative composition of PAHs in the water also changed with time; at 2 d posttreatment, {Sigma} PAH in the lowest treatment reflected contribution from nine PAHs, whereas only two PAHs contributed to this concentration at 84 d. Low and high molecular weight PAHs were lost first from the water column, followed by PAHs of intermediate mol wt. In sediments, a dose-dependent increase in {Sigma} PAH was observed above 0.59 mg/L creosote up to 28 d, followed by a decline thereafter in all but the highest treatment. Total PAHs in sediment ranged from 0.91 {micro}g/g to 63.9 {micro}g/g at 28 d. A dose-dependent relationship was also observed in PVC strips, with {Sigma}PAH on PVC ranging from 0.05 to 88 {micro}g/cm{sup 2} at 31 d and 0.04 to 18.4 {micro}g/cm{sup 2} at 58 d posttreatment. A mass balance evaluation showed that 88.3% of PAHs was lost from the system after 1 month, indicating that liquid creosote is attenuated relatively quickly in aquatic environments.

  6. Analysis and evaluation of interwell seismic logging techniques for hydrocarbon reservoir characterization. Final report

    SciTech Connect

    Parra, J.O.; Zook, B.J.; Sturdivant, V.R.

    1994-06-01

    The work reported herein represents the third year work in evaluating high-resolution interwell seismic logging techniques for hydrocarbon reservoir characterization. The objective of this project is to investigate interwell seismic logging techniques for indirectly interpreting oil and gas reservoir geology and rock physical properties. The work involves a balanced study of theoretical and numerical modeling of seismic waves transmitted between pairs of wells combined with experimental data acquisition and processing at controlled field conditions. The field applications of this reservoir probing concept are aimed at demonstrating high resolution measurements and detailed interpretation of heterogeneous hydrocarbon-bearing formations. The first part of this third year project efforts was devoted to thoroughly evaluating interwell seismic logging and reverse VSP in a hydrocarbon-bearing formation at the Buckhorn test site in Illinois. Specifically, the data from the experiments conducted in the second year of this project were analyzed to delineate geological structures and to extract rock physical parameters. The second part of this project is devoted to the evaluation of continuity logging techniques for hydrocarbon reservoir continuity. Specifically, this part of the project includes the evaluation of methods of measurements, modeling and data processing to delineate the reservoir architecture and relate dispersion and attenuation measurements to rock physical properties.

  7. Quantitative Determination of Saturates, Olefins, and Aromatics in Hydrocarbon Distillate Products Using High-Performance Liquid Chromatography with Dielectric Constant Detection (HPLC-DC).

    DTIC Science & Technology

    high - performance liquid chromatography (HPLC) is the basis of a rapid and accurate hydrocarbon group-type analysis. This novel method can determine saturates, olefins, and total aromatics in hydrocarbon liquids with distillation endpoints of at least 400 deg C. The HPLC separation is achieved using a single, 5-micron olefin-selective column, a backflush valve, and Freon 123 as the mobile phase. The DC detector ensures a genuine uniformity of response (less than 2.5% RSD) for each hydrocarbon group type, independent of the carbon number distribution of

  8. Hydrogen production by reforming of liquid hydrocarbons in a membrane reactor for portable power generation-Experimental studies

    NASA Astrophysics Data System (ADS)

    Damle, Ashok S.

    One of the most promising technologies for lightweight, compact, portable power generation is proton exchange membrane (PEM) fuel cells. PEM fuel cells, however, require a source of pure hydrogen. Steam reforming of hydrocarbons in an integrated membrane reactor has potential to provide pure hydrogen in a compact system. Continuous separation of product hydrogen from the reforming gas mixture is expected to increase the yield of hydrogen significantly as predicted by model simulations. In the laboratory-scale experimental studies reported here steam reforming of liquid hydrocarbon fuels, butane, methanol and Clearlite ® was conducted to produce pure hydrogen in a single step membrane reformer using commercially available Pd-Ag foil membranes and reforming/WGS catalysts. All of the experimental results demonstrated increase in hydrocarbon conversion due to hydrogen separation when compared with the hydrocarbon conversion without any hydrogen separation. Increase in hydrogen recovery was also shown to result in corresponding increase in hydrocarbon conversion in these studies demonstrating the basic concept. The experiments also provided insight into the effect of individual variables such as pressure, temperature, gas space velocity, and steam to carbon ratio. Steam reforming of butane was found to be limited by reaction kinetics for the experimental conditions used: catalysts used, average gas space velocity, and the reactor characteristics of surface area to volume ratio. Steam reforming of methanol in the presence of only WGS catalyst on the other hand indicated that the membrane reactor performance was limited by membrane permeation, especially at lower temperatures and lower feed pressures due to slower reconstitution of CO and H 2 into methane thus maintaining high hydrogen partial pressures in the reacting gas mixture. The limited amount of data collected with steam reforming of Clearlite ® indicated very good match between theoretical predictions and

  9. Pipeline accident effects for hazardous liquid pipelines. Final report

    SciTech Connect

    Greenfeld, J.; Golub, E.; Dresnack, R.; Griffis, F.H.; Pignataro, L.J.

    1996-08-01

    The project team identified the factors that cause pipeline failures and the factors that effect accidents on hazardous liquid pipelines. Since the normalizing of the data was not possible, the authors of this report used indirect and inferential approaches in the analysis. The databases used for this analysis are LIQUID (accident data for 1968-1985) and LIQLCK (accident data for 1985-present). The main finding of this complete data on hazardous liquid accidents should be collected. Other conclusions are that prevention programs should be more effective, and pipe components such as valves, O-rings, gaskets and nipples are a significant source of potentially reducible accidents.

  10. Cement encapsulation of low-level waste liquids. Final report

    SciTech Connect

    Baker, M.N.; Houston, H.M.

    1999-01-01

    Pretreatment of liquid high-level radioactive waste at the West Valley Demonstration Project (WVDP) was essential to ensuring the success of high-level waste (HLW) vitrification. By chemically separating the HLW from liquid waste, it was possible to achieve a significant reduction in the volume of HLW to be vitrified. In addition, pretreatment made it possible to remove sulfates, which posed several processing problems, from the HLW before vitrification took place.

  11. Additives for high temperature liquid lubricants. Final report

    SciTech Connect

    Yavrouian, A.H.; Repar, J.; Moran, C.M.; Lawton, E.A.; Anderson, M.S.

    1994-01-15

    The purpose of this task was to perform research for the Department of Energy (DOE) on the synthesis and characterization of additives for liquid lubricants which could lead to significant improvements in the major tribological task area of friction and wear reduction at high temperature. To this end JPL surveyed candidate precursor compounds which are soluble in liquid lubricants, synthesized the most promising of these materials, characterized them and submitted these additives to National Institute of Standards and Technology (NIST) for evaluation.

  12. Dispersive liquid-liquid microextraction coupled with dispersive micro-solid-phase extraction for the fast determination of polycyclic aromatic hydrocarbons in environmental water samples.

    PubMed

    Shi, Zhi-Guo; Lee, Hian Kee

    2010-02-15

    A new two-step microextraction technique, combining dispersive liquid-liquid microextraction (DLLME) and dispersive microsolid-phase extraction (D-micro-SPE), was developed for the fast gas chromatographic-mass spectrometric determination of polycyclic aromatic hydrocarbons (PAHs) in environmental samples. A feature of the new procedure lies in that any organic solvent immiscible with water can be used as extractant in DLLME. A special apparatus, such as conical-bottom test tubes, and tedious procedures of centrifugation, refrigeration of the solvent, and then thawing it, associated with classical DLLME or similar techniques are not necessary in the new procedure, which potentially lends itself to possible automation. In the present D-micro-SPE approach, hydrophobic magnetic nanoparticles were used to retrieve the extractant of 1-octanol in the DLLME step. It is noteworthy that the target of D-micro-SPE was the 1-octanol rather than the PAHs. Because of the rapid mass transfer associated with the DLLME and the D-micro-SPE steps, fast extraction could be achieved. Parameters affecting the extraction efficiency were investigated in detail. The optimal conditions were as follows: vortex at 3200 rpm in the DLLME step for 2 min and in D-micro-SPE for 1 min and then desorption by sonication for 4 min with acetonitrile as the solvent. The results demonstrated that enrichment factors ranging from 110- to 186-fold were obtained for the analytes. The limits of detection and the limits of quantification were in the range of 11.7-61.4 pg/mL and 0.04-0.21 ng/mL, respectively. The linearities were 0.5-50, 1-50, or 2-50 ng/mL for different PAHs. Finally, the two-step extraction method was successfully used for the fast determination of PAHs in river water samples. This two-step method, combining two different and efficient miniaturized techniques, provides a fast means of sample pretreatment for environmental water samples.

  13. Quantification of polycyclic aromatic hydrocarbons in tea and coffee samples of Mumbai City (India) by high performance liquid chromatography.

    PubMed

    Bishnoi, Narsi R; Mehta, Urvashi; Sain, Umashanker; Pandit, G G

    2005-08-01

    This paper describes a method for quantification of sixteen polycyclic aromatic hydrocarbons (PAHs) in tea and coffee samples of Mumbai City with the help of reversed phase high performance liquid chromatography with UV-VIS detector. This method is based on liquid-liquid extraction followed by clean up with C-18 cartridge. Concentration of total PAHs in different brands of tea and coffee samples varied from 18.79 to 31.37 microg/L and from 16.47 to 18.24 microg/L, respectively. Mean concentration of total PAHs was 27.56 microg/L in tea and 17.20 microg/L in coffee. Recoveries at different concentration levels were higher than 68% in samples of tea and coffee. Detection limit was found to be low (0.0006 ng) for anthracene and highest (0.174 ng) for naphthalene with relative standard deviation between 0.4%-7%.

  14. Method and apparatus for determining the presence or absence of a pour point depressant additive in hydrocarbon liquids

    SciTech Connect

    Rummel, J.D.

    1986-07-29

    A method is described of determining the presence or absence of a pour point depressant additive in a hydrocarbon liquid derived from petroleum, the liquid containing paraffin wax, comprising the steps of: (a) cooling a sample of the liquid at a predetermined cooling rate from a temperature substantially above the cloud point temperature to a temperature substantially below the cloud point temperature; (b) monitoring the slope of the cooling rate curve and noting the points at which a deflection in the curve begins and ends; (c) determining the time interval between the beginning and ending points of the deflection of the curve, and (d) comparing the determined time interval to a reference time interval, associated with the predetermined cooling rate, so as to establish whether the determined time interval is less than or greater than the reference time interval thereby establishing the presence or absence, respectively, of a pour point depressant additive.

  15. Natural gas conversion to higher hydrocarbons using plasma interactions with surfaces. Final report

    SciTech Connect

    Sackinger, W.M.; Kamath, V.A.; Morgan, B.L.; Airey, R.W.

    1993-12-01

    Experiments are reported in which a methane plasma is created, and the methyl ions and hydrogen ions are accelerated within a microchannel array so that they interact with neutral methane molecules on the inside surfaces of the microchannels. No catalysts are used, and the device operates at room temperature. Impact energies of the ions are in the range of 10 eV to greater than 100 eV, and the energy delivered in the interaction at the surfaces causes the production of larger hydrocarbon molecules, such as C{sub 2}H{sub 2}, C{sub 2}H{sub 4}, and C{sub 2}H{sub 6}, along with C{sub 3}, C{sub 4}, C{sub 5}m C{sub 6}, C{sub 7}m and C{sub 8} molecules. There is a decreasing percentage of larger molecules produced, in comparison with the C{sub 2} and C{sub 3} types. Conversion effectiveness is greater at higher pressure, due to the increased ionic activity. The yield of the higher hydrocarbons depends upon the external voltage used, and voltage can be used as a control parameter to adjust the output mixture proportions. A conversion energy of 2.59 kilowatt hours/killogram of output has been demonstrated, and a reduction of this by a factor of 10 is possible using known techniques. In batch experiments, the selectivity for C{sub 2} has varied from 47% to 88%, and selectivity for C{sub 6} has ranged from 0% to 12.8%. Other hydrocarbon selectivities also span a wide and useful range. The estimated costs for hydrocarbons produced with this technology are in the range of $200 per tonne, in production quantities, depending upon natural gas costs. Pilot production experiments are recommended to make these estimates more precise, and to address strategies for scaling the technology up to production levels. Applications are discussed.

  16. Final Technical Report [Polynuclear aromatic hydrocarbons with curved surfaces: Models and precursors for fullerenes

    SciTech Connect

    Radideau, Peter W.

    2001-02-23

    Highlights of selected achievements are briefly outlined. The bowl-to-bowl inversion barrier was measured for a hydrocarbon on the C{sub 60} surface larger than corannulene; {Delta}G was determined to be 27.8 kcal/mol. A new route to the preparation of tetraketone involving benzeneseleninic anhydride was developed that represents a significant improvement in the overall process making semibuckminsterfullerene more accessible. The first crystallographically characterized transition metal buckybowl compound was reported.

  17. Monitoring hydrocarbons and trace metals in Beaufort Sea sediments and organisms. Final report

    SciTech Connect

    Boehm, P.; LeBlanc, L.; Trefry, J.; Marajh-Whittemore, P.; Brown, J.

    1990-10-01

    As part of the Minerals Management Service's environmental studies of oil and gas exploration and production activities in the Alaskan Beaufort Sea, a study was conducted in 1989 to monitor the marine environment for inputs of chemicals related to drilling and exploration. The 1989 Beaufort Sea Monitoring Program (BSMP) was designed to monitor sediments and selected benthic organisms for trace metals and hydrocarbons so as to infer any changes that might have resulted from drilling and production activities. A series of 49 stations were sampled during the program. The study area extended from Cape Halkett on the western end of Harrison Bay to Griffin Point, east of Barter Island. The sampling design combined an area-wide approach in which stations were treated as replicates of 8 specific geographic regions, with an activity-specific approach, which focused on the potential establishment of metal or hydrocarbon concentration gradients with distance from the Endicott Production Field in Prudhoe Bay. The analytical program focused on the analysis of the fine-fraction of the sediment for a series of trace metals and elements and the analysis of a suite of saturated and aromatic hydrocarbons in the bulk sediment. The total organic carbon (TOB) content and the grain size distribution in the sediments were determined as well. Benthic bivalve molluscs, representative of several feeding types were collected from those stations for which data previously existed from the 1984-1986 BSMP, and were analyzed for metals and saturated and aromatic hydrocarbons. The benthic amphipods were collected, pooled by station or region, and analyzed as well.

  18. INTERACTION OF LASER RADIATION WITH MATTER. LASER PLASMA: Laser deposition of amorphous diamond-like films from liquid aromatic hydrocarbons

    NASA Astrophysics Data System (ADS)

    Lyalin, A. A.; Simakin, Aleksandr V.; Bobyrev, V. A.; Lubnin, Evgenii N.; Shafeev, Georgii A.

    1999-04-01

    An experimental investigation was made of the deposition of amorphous diamond-like films on transparent substrates by laser irradiation of the interfaces between such substrates and liquid hydrocarbons [toluene C6H5CH3, benzene C6H6, cumene C6H5CH(CH3)2]. A copper vapour laser (wavelength 510.6 nm, pulse duration 20 ns) was used. The films were studied with x-ray Auger spectroscopy, high-energy electron diffraction, scanning electron microscopy, and Raman scattering spectroscopy. The sp3 fraction in the deposited films reached 50% — 70%, depending on the choice of hydrocarbon. The average film thickness was 100 — 200 nm and the microhardness reached 50 — 70 GPa.

  19. Solvent extraction of low-molecular-weight polycyclic aromatic hydrocarbons from reversed-phase liquid chromatographic effluents

    SciTech Connect

    Ogawa, I.; Chriswell, C.D.

    1982-01-01

    High-performance liquid chromatography provides an effective means of separating constituents of samples of environmental origin. When such samples contain large numbers of constituents at low concentrations, retention times and detector responses provide insufficient data for component characterization. Coupling of HPLC fractionation with GC/MS characterization has proven to be a powerful technique for determining compounds of interest. Reversed-phase HPLC procedures are the most effective for separation of samples containing low-molecular-weight polycyclic aromatic hydrocarbons. However, the aqueous methanol or acetonitrile solvents used with reversed-phase HPLC are incompatible with high-resolution, high-sensitivity gas chromatography. Reversed-phase solvents can be removed from a sample by distillation or by evaporation with an inert gas. Both of these techniques also lead to significant losses of volatile analytes such as low-molecular-weight polycyclic aromatic hydrocarbons. Solvent extraction with large volumes of pentane has been used to isolate polycyclic aromatic hydrocarbons from HPLC effluents containing methanol and from low-pressure liquid chromatographic effluents containing 2-propanol. In the present work it has been demonstrated that low-molecular-weight polycyclic aromatic hydrocarbons can be isolated from reversed-phase HPLC solvents by a one-step solvent extraction using a small volume of solvent. The procedure is rapid and convenient and the use of a small volume of solvent eliminates the need for reducing the volume of extraction solvent by distillation or other techniques. The utility of the method has been demonstrated by the determination of biphenyl on fly ash.

  20. Comparison of air-agitated liquid-liquid microextraction and ultrasound-assisted emulsification microextraction for polycyclic aromatic hydrocarbons determination in hookah water.

    PubMed

    Rajabi, Maryam; Bazregar, Mohammad; Daneshfar, Ali; Asghari, Alireza

    2015-07-01

    In this work, two disperser-free microextraction methods, namely, air-agitated liquid-liquid microextraction and ultrasound-assisted emulsification microextraction are compared for the determination of a number of polycyclic aromatic hydrocarbons in aqueous samples, followed by gas chromatography with flame ionization detection. The effects of various experimental parameters upon the extraction efficiencies of both methods are investigated. Under the optimal conditions, the enrichment factors and limits of detection were found to be in the ranges of 327-773 and 0.015-0.05 ng/mL for air-agitated liquid-liquid microextraction and 406-670 and 0.015-0.05 ng/mL for ultrasound-assisted emulsification microextraction, respectively. The linear dynamic ranges and extraction recoveries were obtained to be in the range of 0.05-120 ng/mL (R(2) ≥ 0.995) and 33-77% for air-agitated liquid-liquid microextraction and 0.05-110 ng/mL (R(2) ≥ 0.994) and 41-67% for ultrasound-assisted emulsification microextraction, respectively. To investigate this common view among some people that smoking hookah is healthy due to the passage of smoke through the hookah water, samples of both the hookah water and hookah smoke were analyzed.

  1. A linearized corrosion double-layer model for laminar flow electrification of hydrocarbon liquids in metal pipes

    SciTech Connect

    Chen, H.; Radke, C.J.; Touchard, G.G.

    1996-09-01

    When a hydrocarbon liquid flows through a metal pipe, an axial streaming current is generated, convected along the pipe, and spilled out into a collection vessel. Flow electrification raises explosion concerns in the petroleum industry. A metal/liquid interface corrosion-reaction model is developed for the flow electrification of low-conductivity liquids in metal pipes. In the proposed model, impurity anions participate in corrosion reaction at the wall, leaving a net positive ion concentration in the diffuse electrical double layer. Convection of this positive charge constitutes the streaming current. Theoretical calculations for the convected space charge density demonstrate a velocity-dependent entrance effect that diminishes in pipes of larger radii, in agreement with experimental data for heptane in stainless steel pipes. Far downstream, the proposed model also correctly predicts that the convected space charge density falls with increasing pipe radius. As in previous work, the convected space charge density far downstream, is found to be linear with the {zeta}-potential. However, the proposed model is self-consistent in that the {zeta}-potential arises as part of the calculation and is not an adjustable constant characteristic only of the metal/hydrocarbon interface.

  2. 29 CFR 1450.24 - Liquidation from final check or recovery from other payment.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... remaining balance on the debt may be made from a final payment of any nature, including but not limited to... 29 Labor 4 2012-07-01 2012-07-01 false Liquidation from final check or recovery from other payment... final check or recovery from other payment. (a) If the employee retires or resigns or if his or...

  3. Salting-out assisted liquid-liquid extraction and partial least squares regression to assay low molecular weight polycyclic aromatic hydrocarbons leached from soils and sediments.

    PubMed

    Bressan, Lucas P; do Nascimento, Paulo Cícero; Schmidt, Marcella E P; Faccin, Henrique; de Machado, Leandro Carvalho; Bohrer, Denise

    2017-02-15

    A novel method was developed to determine low molecular weight polycyclic aromatic hydrocarbons in aqueous leachates from soils and sediments using a salting-out assisted liquid-liquid extraction, synchronous fluorescence spectrometry and a multivariate calibration technique. Several experimental parameters were controlled and the optimum conditions were: sodium carbonate as the salting-out agent at concentration of 2molL(-1), 3mL of acetonitrile as extraction solvent, 6mL of aqueous leachate, vortexing for 5min and centrifuging at 4000rpm for 5min. The partial least squares calibration was optimized to the lowest values of root mean squared error and five latent variables were chosen for each of the targeted compounds. The regression coefficients for the true versus predicted concentrations were higher than 0.99. Figures of merit for the multivariate method were calculated, namely sensitivity, multivariate detection limit and multivariate quantification limit. The selectivity was also evaluated and other polycyclic aromatic hydrocarbons did not interfere in the analysis. Likewise, high performance liquid chromatography was used as a comparative methodology, and the regression analysis between the methods showed no statistical difference (t-test). The proposed methodology was applied to soils and sediments of a Brazilian river and the recoveries ranged from 74.3% to 105.8%. Overall, the proposed methodology was suitable for the targeted compounds, showing that the extraction method can be applied to spectrofluorometric analysis and that the multivariate calibration is also suitable for these compounds in leachates from real samples.

  4. Salting-out assisted liquid-liquid extraction and partial least squares regression to assay low molecular weight polycyclic aromatic hydrocarbons leached from soils and sediments

    NASA Astrophysics Data System (ADS)

    Bressan, Lucas P.; do Nascimento, Paulo Cícero; Schmidt, Marcella E. P.; Faccin, Henrique; de Machado, Leandro Carvalho; Bohrer, Denise

    2017-02-01

    A novel method was developed to determine low molecular weight polycyclic aromatic hydrocarbons in aqueous leachates from soils and sediments using a salting-out assisted liquid-liquid extraction, synchronous fluorescence spectrometry and a multivariate calibration technique. Several experimental parameters were controlled and the optimum conditions were: sodium carbonate as the salting-out agent at concentration of 2 mol L- 1, 3 mL of acetonitrile as extraction solvent, 6 mL of aqueous leachate, vortexing for 5 min and centrifuging at 4000 rpm for 5 min. The partial least squares calibration was optimized to the lowest values of root mean squared error and five latent variables were chosen for each of the targeted compounds. The regression coefficients for the true versus predicted concentrations were higher than 0.99. Figures of merit for the multivariate method were calculated, namely sensitivity, multivariate detection limit and multivariate quantification limit. The selectivity was also evaluated and other polycyclic aromatic hydrocarbons did not interfere in the analysis. Likewise, high performance liquid chromatography was used as a comparative methodology, and the regression analysis between the methods showed no statistical difference (t-test). The proposed methodology was applied to soils and sediments of a Brazilian river and the recoveries ranged from 74.3% to 105.8%. Overall, the proposed methodology was suitable for the targeted compounds, showing that the extraction method can be applied to spectrofluorometric analysis and that the multivariate calibration is also suitable for these compounds in leachates from real samples.

  5. Investigation of the extraction of hydrocarbons from shale ore using supercritical carbon dioxide. Final technical report

    SciTech Connect

    Not Available

    1984-02-01

    Using supercritical carbon dioxide as a solvent, hydrocarbons were extracted from oil shale at low temperature under moderate pressure. Operational variables were studied. The average amount of oil removed corresponded to about 1% of the organic matter of the shale. The maximum yield was 0.73 gallons of oil per ton of shale or about 1.3%. Water was extracted from the shale in greater amounts than was oil. Extraction at temperatures below 400/sup 0/F did not produce high enough yields for the process to be commercially viable. Yield did increase with smaller particle size, increased time of extraction, increased temperature, and increased density of the solvent.

  6. Direct conversion of light hydrocarbon gases to liquid fuel. Quarterly technical status report No. 11 for thrid quarter FY 1990

    SciTech Connect

    Foral, M.J.

    1990-12-31

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

  7. Applications of electrochemically-modulated liquid chromatography (EMLC): Separations of aromatic amino acids and polycyclic aromatic hydrocarbons

    SciTech Connect

    Deng, Li

    1998-03-27

    The research in this thesis explores the separation capabilities of a new technique termed electrochemically-modulated liquid chromatography (EMLC). The thesis begins with a general introduction section which provides a literature review of this technique as well as a brief background discussion of the two research projects in each of the next two chapters. The two papers which follow investigate the application of EMLC to the separation of a mixture of aromatic amino acids and of a mixture of polycyclic aromatic hydrocarbons (PAHs). The last section presents general conclusions and summarizes the thesis. References are compiled in the reference section of each chapter. The two papers have been removed for separate processing.

  8. Direct conversion of light hydrocarbon gases to liquid fuel. Quarterly technical status report No. 23 for second quarter FY 1991

    SciTech Connect

    Foral, M.J.

    1991-12-31

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

  9. Study of the adsorption of aromatic hydrocarbons by marine sediments. Final report

    SciTech Connect

    Henrichs, S.M.; Luoma, M.; Smith, S.

    1997-08-01

    Three aromatic hydrocarbons--benzene, naphthalene, and phenanthrene--were rapidly and strongly adsorbed by intertidal sediments from Jakolof Bay, lower Cook Inlet. Adsorption of phenanthrene was more than twice that of naphthalene and benzene. Adsorption was not completely, rapidly reversible by suspension of the sediment in clean seawater. Longer adsorption reaction times led to decreased desorption, except for benzene. All sites for adsorption on the sediment surface appeared to be equivalent, and availability of adsorption sites did not limit adsorption over the concentration range studied. Adsorption coefficients for phenanthrene varied among sediment samples by as much as a factor of 3. This variability was not correlated with sediment organic carbon content, indicating that organic matter was not solely responsible for the adsorption properties of these sediments. The bioavailability of phenanthrene was decreased by adsorption to sediment. Combined with the finding that adsorption is not completely reversible, these results indicate that adsorption could contribute to the persistence of aromatic hydrocarbons in lower Cook Inlet sediments.

  10. Evaluation of in situ remedial technologies for sites contaminated with hydrocarbons. Final report

    SciTech Connect

    Lige, J.E.; Kunkel, M.L.; MacFarlane, I.D.

    1998-01-01

    This report presents the results of an extensive literature review that was performed to assess the overall effectiveness, applicability, and limitations of the various in situ technologies currently being applied to remediate sites contaminated by petroleum hydrocarbons. Of 17 technologies that were identified in an initial review and database search, nine were selected as widely used or promising for increased future use: soil vapor extraction, bioventing, pump and treat, aquifer air sparging, biosparging, in situ enhanced aquifer bioremediation, natural attenuation, in-well aeration, and dual-phase extraction. Following a general discussion of in situ technology, the report devotes one chapter to each of these nine technologies, presenting in each chapter a description of the technology; criteria to be used in considering applicability of the technology at a site; a discussion of design criteria and operating conditions; a strategy for monitoring remediation and determining when clean-up criteria are met; a discussion of performance-related issues; documented case studies; and a hypothetical application of the technology. Report appendices provide an overview of petroleum hydrocarbon constituents and their properties, and a glossary of terms.

  11. SBIR Final Report. Liquid Core Optical Scintillating Fibers

    SciTech Connect

    Beetz, C.P.; Steinbeck, J.; Buerstler, R.

    2000-05-16

    This Phase I SBIR project focused on developing flexible scintillating liquid core optical fibers, with potential uses in high-energy calorimetry, tracking, preradiators, active targets or other fast detectors. Progress on the six tasks of the project is summarized. The technical developments involve three technology components: (1) highly flexible capillaries or tubes of relatively low n (index of refraction) to serve as cladding and liquid core containment; (2) scintillator (and clear) fluids of relatively high n to serve as a core-- these fluids must have a high light transmission and, for some applications, radiation hardness; (3) optical end plugs, plug insertion, and plug-cladding tube sealing technology to contain the core fluids in the tubes, and to transmit the light.

  12. Evaluation of hydrocarbon flow standard facility equipped with double-wing diverter using four types of working liquids

    NASA Astrophysics Data System (ADS)

    Doihara, R.; Shimada, T.; Cheong, K. H.; Terao, Y.

    2017-06-01

    A flow calibration facility based on the gravimetric method using a double-wing diverter for hydrocarbon flows from 0.1 m3 h-1 to 15 m3 h-1 was constructed as a national measurement standard in Japan. The original working liquids were kerosene and light oil. The calibration facility was modified to calibrate flowmeters with two additional working liquids, industrial gasoline (flash point  >  40 °C) and spindle oil, to achieve calibration over a wide viscosity range at the same calibration test rig. The kinematic viscosity range is 1.2 mm2 s-1 to 24 mm2 s-1. The contributions to the measurement uncertainty due to different types of working liquids were evaluated experimentally in this study. The evaporation error was reduced by using a seal system at the weighing tank inlet. The uncertainty due to droplets from the diverter wings was reduced by a modified diverter operation. The diverter timing errors for all types of working liquids were estimated. The expanded uncertainties for the calibration facility were estimated to be 0.020% for mass flow and 0.030% for volumetric flow for all considered types of liquids. Internal comparisons with other calibration facilities were also conducted, and the agreement was confirmed to be within the claimed expanded uncertainties.

  13. Detailed analysis of petroleum hydrocarbon attenuation in biopiles by high-performance liquid chromatography followed by comprehensive two-dimensional gas chromatography.

    PubMed

    Mao, Debin; Lookman, Richard; Van De Weghe, Hendrik; Van Look, Dirk; Vanermen, Guido; De Brucker, Nicole; Diels, Ludo

    2009-02-27

    Enhanced bioremediation of petroleum hydrocarbons in two biopiles was quantified by high-performance liquid chromatography (HPLC) followed by comprehensive two-dimensional gas chromatography (GCXGC). The attenuation of 34 defined hydrocarbon classes was calculated by HPLC-GCXGC analysis of representative biopile samples at start-up and after 18 weeks of biopile operation. In general, a-cyclic alkanes were most efficiently removed from the biopiles, followed by monoaromatic hydrocarbons. Cycloalkanes and polycyclic aromatic hydrocarbons (PAHs) were more resistant to degradation. A-cyclic biomarkers farnesane, trimethyl-C13, norpristane, pristane and phytane dropped to only about 10% of their initial concentrations. On the other hand, C29-C31 hopane concentrations remained almost unaltered after 18 weeks of biopile operation, confirming their resistance to biodegradation. They are thus reliable indicators to estimate attenuation potential of petroleum hydrocarbons in biopile processed soils.

  14. Features of the sorption redistribution of hydrocarbons and alcohols in a gas-supramolecular liquid crystal system

    NASA Astrophysics Data System (ADS)

    Onuchak, L. A.; Ukolova, D. A.; Burmatnova, T. S.; Kuraeva, Yu. G.; Kuvshinova, S. A.; Burmistrov, V. A.; Stepanova, R. F.

    2015-01-01

    Thermodynamic characteristics of the sorption redistribution of hydrocarbons (C8-C12 n-alkanes, C10H16 terpenes, xylene isomers) and alcohols (C3-C5 alkanols, butanediol-2,3, menthol) in a gas-4-(3-hydroxypropyloxy)-4'-formylazobenzene (HPOFAB) supramolecular smectic-nematic liquid crystal system are studied via inverse gas chromatography. The sorption capacity of HPOFAB with respect to nonmesogene sorbates is found to be strongly diminished due to its associated structure, especially in the smectic A phase. Great positive deviations from the Raoult law in the studied nonmesogene-HPOFAB systems are observed not only in mesophases, but also in the isotropic HPOFAB phase, which has a high selectivity to para- and meta-xylenes, in contrast to the isotropic phases of classic (non-associated) liquid crystals.

  15. A modified microbial adhesion to hydrocarbons assay to account for the presence of hydrocarbon droplets.

    PubMed

    Zoueki, Caroline Warne; Tufenkji, Nathalie; Ghoshal, Subhasis

    2010-04-15

    The microbial adhesion to hydrocarbons (MATH) assay has been used widely to characterize microbial cell hydrophobicity and/or the extent of cell adhesion to hydrophobic liquids. The classical MATH assay involves spectrophotometric absorbance measurements of the initial and final cell concentrations in an aqueous cell suspension that has been contacted with a hydrocarbon liquid. In this study, microscopic examination of the aqueous cell suspension after contact with hexadecane or a hexadecane/toluene mixture revealed the presence of hydrocarbon droplets. The hydrocarbon droplets contributed to the absorbance values during spectrophotometric measurements and caused erroneous estimates of cell concentrations and extents of microbial adhesion. A modified MATH assay that avoids such artefacts is proposed here. In this modified assay, microscopic examination of the aqueous suspension and direct cell counts provides cell concentrations that are free of interference from hydrocarbon droplets. The presence of hydrocarbon droplets was noted in MATH assays performed with three bacterial strains, and two different hydrocarbons, at ionic strengths of 0.2 mM and 20 mM and pH 6. In these experiments, the formation of quasi-stable hydrocarbon droplets cannot be attributed to the presence of biosurfactants, or stabilization by biocolloids. The presence of surface potential at the hydrocarbon-water interface that was characterized by electrophoretic mobility of up to -1 and -2 microm cm/Vs, likely caused the formation of the quasi-stable hydrocarbon droplets that provided erroneous results using the classical MATH assay.

  16. Toluene model for hydrocarbon risk assessment. Final report, 1 January-31 December 1989

    SciTech Connect

    Morre, J.

    1990-05-29

    This project was for continuation of research to investigate the molecular mode of action of a membrane-active hydrocarbon, toluene, potentially present in the Air Force environment as a flight fuel component or from other sources and to serve as a model for other membrane-active molecules in the environment. Two important target sites were identified where rapid dose-dependent but reversible changes in the membrane organization occurred at low dose levels. One of these was at the plasma membrane where the ability of the membrane to form protuberances was severely compromised. The other concerned a failure to form protuberances by membranes involved in internal trafficking between the endoplasmic reticulum and the Golgi apparatus. This step was reproduced in a cell-free system making detailed studies possible. The toluene inhibited step was identified as dependent on ATP hydrolysis. The involved ATPase activity was characterized, solubilized and partially purified.

  17. Status and future opportunities for conversion of synthesis gas to liquid energy fuels: Final report

    SciTech Connect

    Mills, G

    1993-05-01

    The manufacture of liquid energy fuels from syngas (a mixture of H{sub 2} and CO, usually containing CO{sub 2}) is of growing importance and enormous potential because: (1) Abundant US supplies of coal, gas, and biomass can be used to provide the needed syngas. (2) The liquid fuels produced, oxygenates or hydrocarbons, can help lessen environmental pollution. Indeed, oxygenates are required to a significant extent by the Clean Air Act Amendments (CAAA) of 1990. (3) Such liquid synfuels make possible high engine efficiencies because they have high octane or cetane ratings. (4) There is new, significantly improved technology for converting syngas to liquid fuels and promising opportunities for further improvements. This is the subject of this report. The purpose of this report is to provide an account and evaluative assessment of advances in the technology for producing liquid energy fuels from syngas and to suggest opportunities for future research deemed promising for practical processes. Much of the improved technology for selective synthesis of desired fuels from syngas has resulted from advances in catalytic chemistry. However, novel process engineering has been particularly important recently, utilizing known catalysts in new configurations to create new catalytic processes. This report is an update of the 1988 study Catalysts for Fuels from Syngas: New Directions for Research (Mills 1988), which is included as Appendix A. Technology for manufacture of syngas is not part of this study. The manufacture of liquid synfuels is capital intensive. Thus, in evaluating advances in fuels technology, focus is on the potential for improved economics, particularly on lowering plant investment costs. A second important criteria is the potential for environmental benefits. The discussion is concerned with two types of hydrocarbon fuels and three types of oxygenate fuels that can be synthesized from syngas. Seven alternative reaction pathways are involved.

  18. Status and future opportunities for conversion of synthesis gas to liquid energy fuels: Final report

    SciTech Connect

    Mills, G. . Center for Catalytic Science and Technology)

    1993-05-01

    The manufacture of liquid energy fuels from syngas (a mixture of H[sub 2] and CO, usually containing CO[sub 2]) is of growing importance and enormous potential because: (1) Abundant US supplies of coal, gas, and biomass can be used to provide the needed syngas. (2) The liquid fuels produced, oxygenates or hydrocarbons, can help lessen environmental pollution. Indeed, oxygenates are required to a significant extent by the Clean Air Act Amendments (CAAA) of 1990. (3) Such liquid synfuels make possible high engine efficiencies because they have high octane or cetane ratings. (4) There is new, significantly improved technology for converting syngas to liquid fuels and promising opportunities for further improvements. This is the subject of this report. The purpose of this report is to provide an account and evaluative assessment of advances in the technology for producing liquid energy fuels from syngas and to suggest opportunities for future research deemed promising for practical processes. Much of the improved technology for selective synthesis of desired fuels from syngas has resulted from advances in catalytic chemistry. However, novel process engineering has been particularly important recently, utilizing known catalysts in new configurations to create new catalytic processes. This report is an update of the 1988 study Catalysts for Fuels from Syngas: New Directions for Research (Mills 1988), which is included as Appendix A. Technology for manufacture of syngas is not part of this study. The manufacture of liquid synfuels is capital intensive. Thus, in evaluating advances in fuels technology, focus is on the potential for improved economics, particularly on lowering plant investment costs. A second important criteria is the potential for environmental benefits. The discussion is concerned with two types of hydrocarbon fuels and three types of oxygenate fuels that can be synthesized from syngas. Seven alternative reaction pathways are involved.

  19. Quantification of 16 polycyclic aromatic hydrocarbons in cigarette smoke condensate using stable isotope dilution liquid chromatography with atmospheric-pressure photoionization tandem mass spectrometry.

    PubMed

    Zhang, Xiaotao; Hou, Hongwei; Chen, Huan; Liu, Yong; Wang, An; Hu, Qingyuan

    2015-09-17

    A stable isotope dilution liquid chromatography with tandem mass spectrometry method for the analysis of 16 polycyclic aromatic hydrocarbons in cigarette smoke condensate was developed and validated. Compared with previously reported methods, this method has lower limits of detection (0.04-1.35 ng/cig). Additionally, the proposed method saves time, reduces the number of separation steps, and reduces the quantity of solvent needed. The new method was applied to evaluate polycyclic aromatic hydrocarbon content in 213 commercially available cigarettes in China, under the International Standardization Organization smoking regime and the Health Canadian intense smoking regime. The results showed that the total polycyclic aromatic hydrocarbon content was more than two times higher in samples from the Health Canadian intense smoking regime than in samples from the International Standardization Organization smoking regime (1189.23 vs. 2859.50 ng/cig, p<0.05). Meanwhile, the concentration of individual polycyclic aromatic hydrocarbons (and total polycyclic aromatic hydrocarbons) increased with labeled tar content in both of the tested smoking regimes. There was a positive correlation between total polycyclic aromatic hydrocarbons under the International Standardization Organization smoking regime with that under the Health Canadian intense smoking regime. The proposed liquid chromatography with tandem mass spectrometry method is satisfactory for the rapid, sensitive, and accurately quantitative evaluation of polycyclic aromatic hydrocarbon content in cigarette smoke condensate, and it can be applied to assess potential health risks from smoking. This article is protected by copyright. All rights reserved.

  20. Bacterial diversity of a consortium degrading high-molecular-weight polycyclic aromatic hydrocarbons in a two-liquid phase biosystem.

    PubMed

    Lafortune, Isabelle; Juteau, Pierre; Déziel, Eric; Lépine, François; Beaudet, Réjean; Villemur, Richard

    2009-04-01

    High-molecular-weight (HMW) polycyclic aromatic hydrocarbons (PAHs) are pollutants that persist in the environment due to their low solubility in water and their sequestration by soil and sediments. Although several PAH-degrading bacterial species have been isolated, it is not expected that a single isolate would exhibit the ability to degrade completely all PAHs. A consortium composed of different microorganisms can better achieve this. Two-liquid phase (TLP) culture systems have been developed to increase the bioavailability of poorly soluble substrates for uptake and biodegradation by microorganisms. By combining a silicone oil-water TLP system with a microbial consortium capable of degrading HMW PAHs, we previously developed a highly efficient PAH-degrading system. In this report, we characterized the bacterial diversity of the consortium with a combination of culture-dependent and culture-independent methods. Polymerase chain reaction (PCR) of part of the 16S ribosomal RNA gene (rDNA) sequences combined with denaturing gradient gel electrophoresis was used to monitor the bacterial population changes during PAH degradation of the consortium when pyrene, chrysene, and benzo[a]pyrene were provided together or separately in the TLP cultures. No substantial changes in bacterial profiles occurred during biodegradation of pyrene and chrysene in these cultures. However, the addition of the low-molecular-weight PAHs phenanthrene or naphthalene in the system favored one bacterial species related to Sphingobium yanoikuyae. Eleven bacterial strains were isolated from the consortium but, interestingly, only one-IAFILS9 affiliated to Novosphingobium pentaromativorans-was capable of growing on pyrene and chrysene as sole source of carbon. A 16S rDNA library was derived from the consortium to identify noncultured bacteria. Among 86 clones screened, 20 were affiliated to different bacterial species-genera. Only three strains were represented in the screened clones. Eighty

  1. Fundamental studies in production of C{sub 2}-C{sub 4} hydrocarbons from coal. Final report, 1 September 1988--31 August 1992

    SciTech Connect

    Wiser, W.H.; Oblad, A.G.

    1993-03-01

    The following conclusions can be drawn from the result obtained in this kinetic study of single stage coal gasification to hydrocarbon (HC) gases high in C{sub 2}-C{sub 4} hydrocarbons. It was observed that the direct conversion of coal to HC gases involves two steps. The first step is thermal cleavage of the coal structure to produce liquids with small amounts of gases and coke. The second step is conversion of liquids to gases. Coal to liquids occurs very rapidly and was completed within 10 minutes. Liquids to gases is the rate-determining step of the overall process. The conversion of liquids to gases was observed to follow first order kinetics. The first order kinetics treatment of the data by isothermal approximation gave an apparent activation energy of approximately 23 kcal/mol. The first order kinetics treatment of the data by a more rigorous non-isothermal method gave an activation energy of 26 kcal/mol. The quantity of HC gases produced directly from coal reached a constant value of about l0% of the dmmf coal at a reaction time of 10 miutes. Most of the HC gases were produced from the liquids. The study of model compounds shows that conversion of liquids to HC gases.proceeds through a carbonium ion mechanism, and this accounts for the production of C{sub 2}-C{sub 4} gases. Liquid to gases occurs by a catalytic hydrocracking reaction.

  2. Viscosity of defined and undefined hydrocarbon liquids calculated using an extended corresponding-states model

    NASA Astrophysics Data System (ADS)

    Baltatu, M. E.; Chong, R. A.; Huber, M. L.

    1996-01-01

    We predict the viscosity of petroleum fractions using extended corresponding states. Our model builds upon the TRAPP procedure, which is the most advanced approach to predict transport properties of straight-chain nonpolar hydrocarbons and their mixtures. We perform comparisons with experimental viscosity data for pure hydrocarbons, treating them as nonstandard components; we find deviations of 10 15%. We also extend the model to predict the transport properties of petroleum fractions and compare with an experimental database of more than 80 crude oils, including highly aromatic petroleum fractions. The model predicts the viscosity of the crude oil fractions within experimental uncertainty.

  3. Development of gas chromatography-flame ionization detection system with a single column and liquid nitrogen-free for measuring atmospheric C2-C12 hydrocarbons.

    PubMed

    Liu, Chengtang; Mu, Yujing; Zhang, Chenglong; Zhang, Zhibo; Zhang, Yuanyuan; Liu, Junfeng; Sheng, Jiujiang; Quan, Jiannong

    2016-01-04

    A liquid nitrogen-free GC-FID system equipped with a single column has been developed for measuring atmospheric C2-C12 hydrocarbons. The system is consisted of a cooling unit, a sampling unit and a separation unit. The cooling unit is used to meet the temperature needs of the sampling unit and the separation unit. The sampling unit includes a dehydration tube and an enrichment tube. No breakthrough of the hydrocarbons was detected when the temperature of the enrichment tube was kept at -90 °C and sampling volume was 400 mL. The separation unit is a small round oven attached on the cooling column. A single capillary column (OV-1, 30 m × 0.32 mm I.D.) was used to separate the hydrocarbons. An optimal program temperature (-60 ∼ 170 °C) of the oven was achieved to efficiently separate C2-C12 hydrocarbons. There were good linear correlations (R(2)=0.993-0.999) between the signals of the hydrocarbons and the enrichment amount of hydrocarbons, and the relative standard deviation (RSD) was less than 5%, and the method detection limits (MDLs) for the hydrocarbons were in the range of 0.02-0.10 ppbv for sampling volume of 400 mL. Field measurements were also conducted and more than 50 hydrocarbons from C2 to C12 were detected in Beijing city. Copyright © 2015 Elsevier B.V. All rights reserved.

  4. Liquid phase in situ hydrodeoxygenation of biomass-derived phenolic compounds to hydrocarbons over bifunctional catalysts

    Treesearch

    Junfeng Feng; Chung-yun Hse; Zhongzhi Yang; Kui Wang; Jianchun Jiang; Junming Xu

    2017-01-01

    The objective of this study was to find an effective method for converting renewable biomass-derived phenolic compounds into hydrocarbons bio-fuel via in situ catalytic hydrodeoxygenation. The in situ hydrodeoxygenation of biomass-derived phenolic compounds was carried out in methanol-water solvent over bifunctional catalysts of Raney Ni and HZSM-5 or H-Beta. In the in...

  5. Update of on-line coupled liquid chromatography - gas chromatography for the analysis of mineral oil hydrocarbons in foods and cosmetics.

    PubMed

    Biedermann, Maurus; Munoz, Celine; Grob, Koni

    2017-09-13

    On-line coupled high performance liquid chromatography-gas chromatography-flame ionization detection (HPLC-GC-FID) is the most widely used method for the analysis of mineral oil hydrocarbons in food, food contact materials, tissues and cosmetics. With comprehensive two-dimensional gas chromatography (GCxGC), a tool became available for better establishing the elution sequence of the various types of hydrocarbons from the HPLC column used for isolating the mineral oil saturated hydrocarbons (MOSH) and mineral oil aromatic hydrocarbons (MOAH). The performance of a heavily used HPLC column with reduced retention for MOAH was investigated to improve the robustness of the method. Updates are recommended that render the MOSH/MOAH separation less dependent of the state of the HPLC column and more correct in cases of highly refined mineral oil products of high molecular mass. Cyclohexyl cyclohexane (Cycy), used as internal standard, turned out to be eluted slightly after cholestane (Cho); apparently the size exclusion effect predominates the extra retention by ring number on the 60Å pore size silica gel. Hence, Cycy can be used to determine the end of the MOSH fraction. Long chain alkyl benzenes were eluted earlier than tri-tert. butyl benzene (Tbb). It is proposed to start the MOAH transfer immediately after the MOSH fraction and use a gradient causing breakthrough of dichloromethane (visible in the UV chromatogram) at a time suitable to elute perylene (Per) at the end of the fraction. In this way, a decrease in retention power of the HPLC column can be tolerated without adjustment of the MOAH fraction until some MOAH start being eluted into the MOSH fraction. This critical point can be checked either with di(2-ethylhexyl) benzene (DEHB) as a marker or the HPLC-UV chromatogram. Finally, based on new findings in rats and human tissues, it is recommended to integrate the MOSH and MOAH up to the retention time of the n-alkane C40. Copyright © 2017 Elsevier B.V. All rights

  6. Trace determination of volatile polycyclic aromatic hydrocarbons in natural waters by magnetic ionic liquid-based stir bar dispersive liquid microextraction.

    PubMed

    Benedé, Juan L; Anderson, Jared L; Chisvert, Alberto

    2018-01-01

    In this work, a novel hybrid approach called stir bar dispersive liquid microextraction (SBDLME) that combines the advantages of stir bar sorptive extraction (SBSE) and dispersive liquid-liquid microextraction (DLLME) has been employed for the accurate and sensitive determination of ten polycyclic aromatic hydrocarbons (PAHs) in natural water samples. The extraction is carried out using a neodymium stir bar magnetically coated with a magnetic ionic liquid (MIL) as extraction device, in such a way that the MIL is dispersed into the solution at high stirring rates. Once the stirring is ceased, the MIL is magnetically retrieved onto the stir bar, and subsequently subjected to thermal desorption (TD) coupled to a gas chromatography-mass spectrometry (GC-MS) system. The main parameters involved in TD, as well as in the extraction step affecting the extraction efficiency (i.e., MIL amount, extraction time and ionic strength) were evaluated. Under the optimized conditions, the method was successfully validated showing good linearity, limits of detection and quantification in the low ng L(-1) level, good intra- and inter-day repeatability (RSD < 13%) and good enrichment factors (18 - 717). This sensitive analytical method was applied to the determination of trace amounts of PAHs in three natural water samples (river, tap and rainwater) with satisfactory relative recovery values (84-115%), highlighting that the matrices under consideration do not affect the extraction process. Copyright © 2017 Elsevier B.V. All rights reserved.

  7. Optimization of two different dispersive liquid-liquid microextraction methods followed by gas chromatography-mass spectrometry determination for polycyclic aromatic hydrocarbons (PAHs) analysis in water.

    PubMed

    Tseng, Wan-Chi; Chen, Pai-Shan; Huang, Shang-Da

    2014-03-01

    Novel sample preparation methods termed "up-and-down shaker-assisted dispersive liquid-liquid microextraction (UDSA-DLLME)" and "water with low concentration of surfactant in dispersed solvent-assisted emulsion dispersive liquid-liquid microextraction (WLSEME)" coupled with gas chromatography-mass spectrometry (GC-MS) have been developed for the analysis of 11 polycyclic aromatic hydrocarbons (PAHs) in aqueous samples. For UDSA-DLLME, an up-and-down shaker-assisted emulsification was employed. Extraction was complete in 3min. Only 14 μL of 1-heptanol was required, without a dispersive solvent. Under the optimum conditions, the linear range was 0.08-100 µg L(-1), and the LODs were in the range 0.022-0.060 µg L(-1). The enrichment factors (EFs) ranged from 392 to 766. Relative recoveries were between 84% and 113% for river, lake, and field water. In WLSEME, 9 μL of 1-nonanol as extraction solvent and 240 μL of 1 mg L(-1) Triton X-100 as surfactant were mixed in a microsyringe to form a cloudy emulsified solution, which was then injected into the samples. Compared with other surfactant-assisted emulsion methods, WLSEME uses much less surfactant. The linear range was 0.08-100 µg L(-1), and the LODs were 0.022-0.13 µg L(-1). The EFs ranged from 388 to 649. The relative recoveries were 86-114% for all three water specimens.

  8. Isotope Fractionation by Diffusion in Liquids (Final Technical Report)

    SciTech Connect

    Richter, Frank

    2016-11-09

    The overall objective of the DOE-funded research by grant DE-FG02-01ER15254 was document and quantify kinetic isotope fractionations during chemical and thermal (i.e., Soret) diffusion in liquids (silicate melts and water) and in the later years to include alloys and major minerals such as olivine and pyroxene. The research involved both laboratory experiments and applications to natural settings. The key idea is that major element zoning on natural geologic materials is common and can arise for either changes in melt composition during cooling and crystallization or from diffusion. The isotope effects associated with diffusion that we have documented are the key for determining whether or not the zoning observed in a natural system was the result of diffusion. Only in those cases were the zoning is demonstrably due to diffusion can use independently measured rates of diffusion to constrain the thermal evolution of the system.

  9. Analysis of soil and house dust for polycyclic aromatic hydrocarbons. Final report, July 1995-January 1996

    SciTech Connect

    Chuang, J.C.

    1996-07-01

    It has been conjectured that jet turbine exhaust near airplane flight paths may result in significant human exposure to Polycyclic Aromatic Hydrocarbons (PAHs). The EPA Risk Reduction Engineering Laboratory (RREL) arranged access to a household located approximately eight miles from the end of a runway at the Greater Cincinnati and Northern Kentucky Airport, and collected soil, wipe, and dust samples in and around the household. A total of 19 PAH ranging from naphthalene (2-ring) to coronene (7-ring) were measured. The general concentration trend for the 19 PAH is house dust > entryway dust > soil. The house dust samples were colleted inside the household and the entryway dust and soil samples were collected outside. Seven of the target PAH are ranked as probable human carcinogens (B2) in the U.S. EPA`s Integrated Risk Information System. The concentrations of B2 PAH account for roughly half of the concentrations of the sums of 19 PAH in most soil and dust samples but not in wipe samples.

  10. Final Report: Thermal Conductance of Solid-Liquid Interfaces

    SciTech Connect

    Cahil, David, G.; Braun, Paul, V.

    2006-05-31

    Research supported by this grant has significantly advanced fundamental understanding of the thermal conductance of solid-liquid interfaces, and the thermal conductivity of nanofluids and nanoscale composite materials. • The thermal conductance of interfaces between carbon nanotubes and a surrounding matrix of organic molecules is exceptionally small and this small value of the interface conductance limits the enhancement in thermal conductivity that can be achieved by loading a fluid or a polymer with nanotubes. • The thermal conductance of interfaces between metal nanoparticles coated with hydrophilic surfactants and water is relatively high and surprisingly independent of the details of the chemical structure of the surfactant. • We extended our experimental methods to enable studies of planar interfaces between surfactant-coated metals and water where the chemical functionalization can be varied between strongly hydrophobic and strongly hydrophilic. The thermal conductance of hydrophobic interfaces establishes an upper-limit of 0.25 nm on the thickness of the vapor-layer that is often proposed to exist at hydrophobic interfaces. • Our high-precision measurements of fluid suspensions show that the thermal conductivity of fluids is not significantly enhanced by loading with a small volume fraction of spherical nanoparticles. These experimental results directly contradict some of the anomalous results in the recent literature and also rule-out proposed mechanisms for the enhanced thermal conductivity of nanofluids that are based on modification of the fluid thermal conductivity by the coupling of fluid motion and the Brownian motion of the nanoparticles.

  11. Hydrocarbon autothermal reforming program. Final technical report, 28 September 1979-31 October 1981

    SciTech Connect

    Ham, D.O.; Lewis, P.F.; Lord, G.W.; Yarrington, R.M.; Hwang, H.S.

    1982-02-01

    The goal of the PSI program was to understand the mechanisms of the formation of carbon deposits under conditions relevant to authothermal reformers (ATR). The first year of this two year program was dedicated almost entirely to investigations of gas phase soot formation. It was speculated that soot could form in the gas phase and deposit downstream in the catalyst bed. A high temperature experimental test rig was constructed and comptuer models developed to aid in understanding this process. The conclusion of these studies is that soot does not form in the gas phase upstream of the catalyst bed, under ATR conditions, at least, not under well mixed conditions. In the second year, the program was redirected to study carbon formation processes on surfaces and to perform testing and analysis of Engelhard's six inch ATR rig. This work has resulted in an operational computer code for use in modeling the Engelhard ATR. This code requires rate constant information for performance prediction. The PSI laboratory experiments have shown that coke formation on surfaces of nickel catalysts is very rapid, particularly from olefins. Filamentary carbon was formed. Various relevant processes and their relative rates were studied on various nickel surfaces. Coke was not observed when precious metal catalysts were used. Testing on the Engelhard reactor was performed. These preliminary tests show that the Engelhard catalysts can be used to reform number two fuel oil with no problems associated with carbonaceous deposits. Some hydrocarbon breakthrough was observed, increasing at low oxygen to carbon ratio (0.355). These limited data clearly indicate a high potential for a useful ATR. Further testing and analysis are clearly necessary.

  12. Apparatus and methods for direct conversion of gaseous hydrocarbons to liquids

    DOEpatents

    Kong, Peter C.; Lessing, Paul A.

    2006-04-25

    A chemical reactor for direct conversion of hydrocarbons includes a dielectric barrier discharge plasma cell and a solid oxide electrochemical cell in fluid communication therewith. The discharge plasma cell comprises a pair of electrodes separated by a dielectric material and passageway therebetween. The electrochemical cell comprises a mixed-conducting solid oxide electrolyte membrane tube positioned between a porous cathode and a porous anode, and a gas inlet tube for feeding oxygen containing gas to the porous cathode. An inlet is provided for feeding hydrocarbons to the passageway of the discharge plasma cell, and an outlet is provided for discharging reaction products from the reactor. A packed bed catalyst may optionally be used in the reactor to increase efficiency of conversion. The reactor can be modified to allow use of a light source for directing ultraviolet light into the discharge plasma cell and the electrochemical cell.

  13. Liquid viscosities of carbon dioxide + hydrocarbons from 310 K to 403 K

    SciTech Connect

    Barrufet, M.A.; El-Sayed Salem, S.K.; Tantawy, M.; Iglesias-Silva, G.A.

    1996-05-01

    A knowledge of the effect of CO{sub 2} upon the properties of a hydrocarbon mixture is essential to evaluate how viscous fingering, gravity segregation, hydrodynamic dispersion, and interfacial tension phenomena affect the local displacement efficiency in a miscible gas flooding process. Kinematic viscosities of twelve mixtures made from pentane, hexane, heptane, octane, decane, and carbon dioxide were measured using a rolling ball viscometer. The temperatures ranged from 310 K to 403 K and the pressures from 0.8 MPa to 12 MPa. Kinematic viscosities were converted to absolute viscosities using mixture densities estimated from a modified Rackett equation. Calculated absolute viscosities for the decane + CO{sub 2} system were within 0.5% of the values by Cullick and Mathis. All viscosities of hydrocarbon mixtures and hydrocarbons with CO{sub 2} could be predicted from the Orbey and Sandler correlation with an average absolute deviation of 4.1%. The authors found that the Lohrenz, Bray, and Clark viscosity correlation cannot be used to estimate the viscosity of the mixtures containing CO{sub 2} with reasonable accuracy.

  14. A novel dispersive liquid-liquid microextraction based on solidification of floating organic droplet method for determination of polycyclic aromatic hydrocarbons in aqueous samples.

    PubMed

    Xu, Hui; Ding, Zongqing; Lv, Lili; Song, Dandan; Feng, Yu-Qi

    2009-03-16

    A new dispersive liquid-liquid microextraction based on solidification of floating organic droplet method (DLLME-SFO) was developed for the determination of five kinds of polycyclic aromatic hydrocarbons (PAHs) in environmental water samples. In this method, no specific holder, such as the needle tip of microsyringe and the hollow fiber, is required for supporting the organic microdrop due to the using of organic solvent with low density and proper melting point. Furthermore, the extractant droplet can be collected easily by solidifying it in the lower temperature. 1-Dodecanol was chosen as extraction solvent in this work. A series of parameters that influence extraction were investigated systematically. Under optimal conditions, enrichment factors (EFs) for PAHs were in the range of 88-118. The limit of detections (LODs) for naphthalene, diphenyl, acenaphthene, anthracene and fluoranthene were 0.045, 0.86, 0.071, 1.1 and 0.66ngmL(-1), respectively. Good reproducibility and recovery of the method were also obtained. Compared with the traditional liquid-phase microextraction (LPME) and dispersive liquid-liquid microextraction (DLLME) methods, the proposed method obtained about 2 times higher enrichment factor than those in LPME. Moreover, the solidification of floating organic solvent facilitated the phase transfer. And most importantly, it avoided using high-density and toxic solvent in the traditional DLLME method. The proposed method was successfully applied to determinate PAHs in the environmental water samples. The simple and low-cost method provides an alternative method for the analysis of non-polar compounds in complex environmental water.

  15. Determination of polycyclic aromatic hydrocarbons in milk samples by high-performance liquid chromatography with fluorescence detection.

    PubMed

    Kishikawa, Naoya; Wada, Mitsuhiro; Kuroda, Naotaka; Akiyama, Syuzo; Nakashima, Kenichiro

    2003-06-15

    This paper describes a high-performance liquid chromatographic (HPLC) method for the determination of polycyclic aromatic hydrocarbons (PAHs) in milk samples. The method involves a liquid-liquid extraction procedure after saponification of milk samples with sodium hydroxide. Reproducible determination with highly sensitive detection was attained by HPLC with fluorescence detection using 1,2-bis(9-anthryl)ethane as an internal standard. The detection limits of 12 kinds of PAHs ranged from 1.3 to 76 ng/kg milk at a signal/noise ratio of 3. By the proposed method, the presence of 12 and 11 kinds of PAHs could be confirmed in commercial milk and human milk samples, respectively. The average concentrations of total PAHs (mean+/-SD, micro g/kg) were found to be 0.99+/-0.37 for commercial milk (n=14), 2.01+/-0.30 for infant formula (n=3) and 0.75+/-0.47 for human milk (n=51). High correlation coefficients between the concentrations of total PAHs and triglyceride were observed for commercial milk (r=0.659) and human milk (r=0.645).

  16. Conversion of methane to higher hydrocarbons (Biomimetic catalysis of the conversion of methane to methanol). Final report

    SciTech Connect

    Watkins, B.E.; Taylor, R.T.; Satcher, J.H.

    1993-09-01

    In addition to inorganic catalysts that react with methane, it is well-known that a select group of aerobic soil/water bacteria called methanotrophs can efficiently and selectively utilize methane as the sole source of their energy and carbon for cellular growth. The first reaction in this metabolic pathway is catalyzed by the enzyme methane monooxygenase (MMO) forming methanol. Methanol is a technology important product from this partial oxidation of methane since it can be easily converted to liquid hydrocarbon transportation fuels (gasoline), used directly as a liquid fuel or fuel additive itself, or serve as a feedstock for chemicals production. This naturally occurring biocatalyst (MMO) is accomplishing a technologically important transformation (methane directly to methanol) for which there is currently no analogous chemical (non-biological) process. The authors approach has been to use the biocatalyst, MMO, as the initial focus in the development of discrete chemical catalysts (biomimetic complexes) for methane conversion. The advantage of this approach is that it exploits a biocatalytic system already performing a desired transformation of methane. In addition, this approach generated needed new experimental information on catalyst structure and function in order to develop new catalysts rationally and systematically. The first task is a comparative mechanistic, biochemical, and spectroscopic investigation of MMO enzyme systems. This work was directed at developing a description of the structure and function of the catalytically active sites in sufficient detail to generate a biomimetic material. The second task involves the synthesis, characterization, and chemical reactions of discrete complexes that mimic the enzymatic active site. These complexes were synthesized based on their best current understanding of the MMO active site structure.

  17. High-pressure cylindrical acoustic resonance diffusion measurements of methane in liquid hydrocarbons

    SciTech Connect

    Colgate, S.O.; House, V.E.; Thieu, V.

    1995-05-01

    A novel cylindrical acoustic resonance method for the measurement of gas diffusion into liquids at high pressures is described. The measurements were performed in a vertically oriented cylindrical acoustic resonator containing both the liquid solvent and gaseous diffusant while under high-precision isothermal and isobaric control. Individual resonance modes of the liquid column, the gas column, and the two-phase coupled fluid are resolved in the last Fourier transform acoustic-resonance spectrum (FFT-ARS). High-resolution acoustic spectra measured at frequent time intervals reveal the changes which accompany the diffusion of gas into the liquid phase. One change, namely, the growth in length of the liquid column, results in a systematic shift to higher frequencies of axial modes in the gas column. The temporal behavior of this moving boundary, together with quantitative measurement of the flow to the gas column required to sustain the constant pressure, permits determination of the gas-into-liquid diffusion coefficient. Diffusion coefficients were determined from the change in frequency as a function of time of axial resonance modes in the gas-phase virtual cylinder as the surface of the underlying liquid phase advanced due to gas absorption. Measurements of the systems methane/n-octane, methane/n-nonane, and methane/n-decane were performed as a function of temperature at a pressure of 250 psia. Comparisons is made to results obtained elsewhere and by other methods but at the same temperatures and pressure.

  18. MEASUREMENT OF HIGH-MOLECULAR-WEIGHT POLYCYCLIC AROMATIC HYDROCARBONS IN SOILS BY PARTICLE BEAM HIGH-PERFORMANCE LIQUID CHROMATOGRAPHY-MASS SPECTROMETRY

    EPA Science Inventory

    Polycyclic aromatic hydrocarbons (PAHs) comprise a class of potentially hazardous compounds of concern to the U.S.EPA. The application of particle-beam (PB) liquid chromatography-mass spectrometry (LC-MS) to the measurement of high-molecular-weight PAHs was investigated. Instrume...

  19. Laser-enhanced synthesis and processing of diamond films from liquid hydrocarbons

    NASA Technical Reports Server (NTRS)

    Singh, Jogender; Vellaikal, M.; Narayan, J.

    1993-01-01

    We report synthesis of diamond films by pulsed laser irradiation on copper substrate immersed into liquid benzene. It is envisaged that carbon released from benzene at the liquid-solid interface is converted into diamond as a result of rapid quenching from a high temperature. The diamond crystallites were characterized using high resolution transmission electron microscopy imaging and electron diffraction techniques. Growth of thicker diamond films by subsequent chemical vapor deposition has been investigated by transmission and scanning electron microscopy techniques. Thin diamond film deposited during liquid phase provided seed for diamond growth during subsequent chemical vapor deposition.

  20. Laser-enhanced synthesis and processing of diamond films from liquid hydrocarbons

    NASA Technical Reports Server (NTRS)

    Singh, Jogender; Vellaikal, M.; Narayan, J.

    1993-01-01

    We report synthesis of diamond films by pulsed laser irradiation on copper substrate immersed into liquid benzene. It is envisaged that carbon released from benzene at the liquid-solid interface is converted into diamond as a result of rapid quenching from a high temperature. The diamond crystallites were characterized using high resolution transmission electron microscopy imaging and electron diffraction techniques. Growth of thicker diamond films by subsequent chemical vapor deposition has been investigated by transmission and scanning electron microscopy techniques. Thin diamond film deposited during liquid phase provided seed for diamond growth during subsequent chemical vapor deposition.

  1. Renewable liquid fuels from catalytic reforming of biomass-derived oxygenated hydrocarbons

    NASA Astrophysics Data System (ADS)

    Barrett, Christopher J.

    Diminishing fossil fuel reserves and growing concerns about global warming require the development of sustainable sources of energy. Fuels for use in the transportation sector must have specific physical properties that allow for efficient distribution, storage, and combustion; these requirements are currently fulfilled by petroleum-derived liquid fuels. The focus of this work has been the development of two new biofuels that have the potential to become widely used transportation fuels from carbohydrate intermediates. Our first biofuel has cetane numbers ranging from 63 to 97 and is comprised of C7 to C15 straight chain alkanes. These alkanes can be blended with diesel like fuels or with P-series biofuel. Production involves a solid base catalyzed aldol condensation with mixed Mg-Al-oxide between furfural or 5-hydroxymethylfurfural (HMF) and acetone, followed by hydrogenation over Pd/Al2O3, and finally hydrogenation/dehydration over Pt/SiO2-Al2O3. Water was the solvent for all process steps, except for the hydrogenation/dehydration stage where hexadecane was co-fed to spontaneously separate out all alkane products and eliminate the need for energy intensive distillation. A later optimization identified Pd/MgO-ZrO2 as a hydrothermally stable bifunctional catalyst to replace Pd/Al2O3 and the hydrothermally unstable Mg-Al-oxide catalysts along with optimizing process parameters, such as temperature and molar ratios of reactants to maximize yields to heavier alkanes. Our second biofuel involved creating an improved process to produce HMF through the acid-catalyzed dehydration of fructose in a biphasic reactor. Additionally, we developed a technique to further convert HMF into 2,5-dimethylfuran (DMF) by hydrogenolysis of C-O bonds over a copper-ruthenium catalyst. DMF has many properties that make it a superior blending agent to ethanol: it has a high research octane number at 119, a 40% higher energy density than ethanol, 20 K higher boiling point, and is insoluble in

  2. Research activities in modeling the selective oxidation of hydrocarbons. Final report

    SciTech Connect

    Rappe, A.

    1995-12-01

    Selective oxidation of organic substrates by oxygen, where all 4 oxidizing equivalents are used productively, remains an unsolved problem in catalysis. In an idealized catalytic cycle that could solve this problem, three separate steps are involved: first oxygen must be rapidly bound, then the O-O bond must be cleaved, and finally each oxo ligand needs to react independently with the substrate regenerating the catalyst. The first and last steps were investigated in this research program. Molecular mechanics was used to study the O{sub 2} binding step and ab initio electronic structure tools were used to study M-O bonding and the reactivity of M{double_bond}O bonds with methane. Mn and Fe complexes are involved.

  3. A mild, chemical conversion of cellulose to hexene and other liquid hydrocarbon fuels and additives

    SciTech Connect

    Robinson, J.M.

    1995-12-31

    A unique biomass fractionation is used to feed a novel chemical reduction process that converts carbohydrates with 100% carbon conversion into hydrocarbon fuels. Six strategic goals have been accomplished: (1) Lignin is cleanly removed in a single step, (2) The carbon chain of the sugar monomers remains intact, (3) Each reaction occurs at mild conditions and gives essentially quantitative yield, (4) Each reaction is catalytic, (5) Initial reactions occur in an aqueous medium, which (6) allows the use of wet feedstocks. Catalytic recycling of the chemical reducing agents thus provides the equivalent of an efficient biomass reduction. Conversion of cellulose (1) to hexenes (8) sequentially via sorbitol (4) and 2-iodohexane (6) typifies the process. Step 2 of the process is highly tunable and can directly produce about 80% hydrocarbon oligomers, C{sub 12}H{sub 22} (12) and C{sub 18}H{sub 32} (13). Oxygenate fuel additives such as 2-hexanol (14) are also available by further reactions of hexene.

  4. Novel process for depolymerization of coal to C{sub 2}-C{sub 4} hydrocarbons. Final report, 1 September 1989--31 August 1993

    SciTech Connect

    Wiser, W.H.; Oblad, A.G.

    1994-07-08

    A principal objective of this work was to study the conversion of coal to C{sub 2} {minus} C{sub 4} hydrocarbons in a two-stage reactor system. Coal was converted to liquids at 440{degrees}C in a stirred batch autoclave using tetralin as the hydrogen donor solvent. The liquids produced were separated from the unreacted coal and ash by filtration. The liquids were then fed into a second stage fixed bed reactor containing sulfided Ni-Mo/Al{sub 2}O{sub 3} and SiO{sub 2{minus}}Al{sub 2}O{sub 3} catalyst. The liquids were hydrocracked on the dual functional catalyst giving high yields of C{sub 2} {minus} C{sub 4}. hydrocarbons. The pressure was 1800 psi and the temperatures were in the range of 425 to 500{degrees}C. The kinetic parameters of the conversion of coal liquids to gases were determined. The activation energy was determined.

  5. Understanding of catalyst deactivation caused by sulfur poisoning and carbon deposition in steam reforming of liquid hydrocarbon fuels

    NASA Astrophysics Data System (ADS)

    Xie, Chao

    2011-12-01

    The present work was conducted to develop a better understanding on the catalyst deactivation in steam reforming of sulfur-containing liquid hydrocarbon fuels for hydrogen production. Steam reforming of Norpar13 (a liquid hydrocarbon fuel from Exxon Mobile) without and with sulfur was performed on various metal catalysts (Rh, Ru, Pt, Pd, and Ni) supported on different materials (Al2O3, CeO2, SiO2, MgO, and CeO2- Al2O3). A number of characterization techniques were applied to study the physicochemical properties of these catalysts before and after the reactions. Especially, X-ray absorption near edge structure (XANES) spectroscopy was intensively used to investigate the nature of sulfur and carbon species in the used catalysts to reveal the catalyst deactivation mechanism. Among the tested noble metal catalysts (Rh, Ru, Pt, and Pd), Rh catalyst is the most sulfur tolerant. Al2O3 and CeO2 are much better than SiO2 and MgO as the supports for the Rh catalyst to reform sulfur-containing hydrocarbons. The good sulfur tolerance of Rh/Al2O3 can be attributed to the acidic nature of the Al2O3 support and its small Rh crystallites (1-3 nm) as these characteristics facilitate the formation of electron-deficient Rh particles with high sulfur tolerance. The good catalytic performance of Rh/CeO2 in the presence of sulfur can be ascribed to the promotion effect of CeO2 on carbon gasification, which significantly reduced the carbon deposition on the Rh/CeO2catalyst. Steam reforming of Norpar13 in the absence and presence of sulfur was further carried out over CeO2-Al2O3 supported monometallic Ni and Rh and bimetallic Rh-Ni catalysts at 550 and 800 °C. Both monometallic catalysts rapidly deactivated at 550 °C, iv and showed poor sulfur tolerance. Although ineffective for the Ni catalyst, increasing the temperature to 800 °C dramatically improved the sulfur tolerance of the Rh catalyst. Sulfur K-edge XANES revealed that metal sulfide and organic sulfide are the dominant sulfur

  6. Bubble curves and saturated liquid molar volumes for chlorofluorohydrocarbon-hydrocarbon mixtures: Experimental data and modeling

    SciTech Connect

    Laugier, S. ); Richon, D.; Renon, H. . Lab. de Thermodynamique)

    1994-01-01

    Vapor-liquid equilibria and liquid densities were obtained using a static apparatus fitted with a variable-volume cell which was described in detail by Valtz et al. (1). Results are given at four temperatures for the binary systems butane--1,2,2-trichlorotrifluoroethane, pentane--1,2-dichloro-1,1,2,2-tetrafluoroethane, hexane--1,2-dichloro-1,1,2,2-tetrafluoroethane, heptane--1,12-trichloro-1,2,2-trifluoromethane, heptane--1,2-dichloro-1,1,2,2-tetrafluoroethane, and benzene--1,2-dichloro-1,1,2,2-tetrafluoroethane and the ternary system 1,2-dichloro-1,1,2,2-tetrafluoroethane--1,1,2-trichloro-1,2,2-trifluoromethane--heptane. The best simultaneous representation of pressures and saturated liquid molar volumes at a given temperature and liquid composition for these mixtures is obtained using either the Patel-Teja or Trebble-Bishnoi-Salim equation of state (TBS EOS) in either their standard or generalized form (maximum deviation 0.7% in pressure and 3.1% in saturated liquid molar volume with the TBS EOS).

  7. Coupling of homogeneous liquid-liquid extraction and dispersive liquid-liquid microextraction for the extraction and preconcentration of polycyclic aromatic hydrocarbons from aqueous samples followed by GC with flame ionization detection.

    PubMed

    Farajzadeh, Mir Ali; Khiavi, Elahe Behboudi; Khorram, Parisa; Mogaddam, Mohammad Reza Afshar

    2017-01-01

    In the present study, a simple and rapid method for the extraction and preconcentration of some polycyclic aromatic hydrocarbons in water samples has been developed. In this method, two sample preparation methods were combined to obtain high extraction recoveries and enrichment factors for sensitive analysis of the selected analytes. In the first stage of the method, a homogeneous solution containing an aqueous solution and cyclohexyl amine is broken by the addition of a salt. After centrifugation, the upper collected phase containing the extracted analytes is subjected to the following dispersive liquid-liquid microextraction method. Rapid injection of the mixture of cyclohexyl amine resulted from the first stage and 1,1,2-trichloroethane (as an extraction solvent) into an acetic acid solution is led to form a cloudy solution. After centrifuging, the fine droplets of the extraction solvent are settled down in the bottom of the test tube, and an aliquot of it is analyzed by gas chromatography. Under the optimum extraction conditions, enrichment factors and limits of detection for the studied analytes were obtained in the ranges of 616-752 and 0.08-0.20 μg/L, respectively. The simplicity, high extraction efficiency, short sample preparation time, low cost, and safety demonstrated the efficiency of this method relative to other approaches.

  8. π-electron S = ½ quantum spin-liquid state in an ionic polyaromatic hydrocarbon

    NASA Astrophysics Data System (ADS)

    Takabayashi, Yasuhiro; Menelaou, Melita; Tamura, Hiroyuki; Takemori, Nayuta; Koretsune, Takashi; Štefančič, Aleš; Klupp, Gyöngyi; Buurma, A. Johan C.; Nomura, Yusuke; Arita, Ryotaro; Arčon, Denis; Rosseinsky, Matthew J.; Prassides, Kosmas

    2017-07-01

    Molecular solids with cooperative electronic properties based purely on π electrons from carbon atoms offer a fertile ground in the search for exotic states of matter, including unconventional superconductivity and quantum magnetism. The field was ignited by reports of high-temperature superconductivity in materials obtained by the reaction of alkali metals with polyaromatic hydrocarbons, such as phenanthrene and picene, but the composition and structure of any compound in this family remained unknown. Here we isolate the binary caesium salts of phenanthrene, Cs(C14H10) and Cs2(C14H10), to show that they are multiorbital strongly correlated Mott insulators. Whereas Cs2(C14H10) is diamagnetic because of orbital polarization, Cs(C14H10) is a Heisenberg antiferromagnet with a gapped spin-liquid state that emerges from the coupled highly frustrated Δ-chain magnetic topology of the alternating-exchange spiral tubes of S = ½ (C14H10)•- radical anions. The absence of long-range magnetic order down to 1.8 K (T/J ≈ 0.02 J is the dominant exchange constant) renders the compound an excellent candidate for a spin-½ quantum-spin liquid (QSL) that arises purely from carbon π electrons.

  9. Solid phase microextraction assisted by droplets-based liquid-liquid microextraction for analysis of volatile aromatic hydrocarbons in water by gas chromatography.

    PubMed

    Ciucanu, Ionel; Agotici, Vlad

    2012-07-01

    A new technique for the analysis of volatile aromatic hydrocarbons by combining liquid-liquid microextraction with solid phase microextraction has been developed. The analytes were extracted from aqueous samples by an immobilized polydimethylsiloxane fiber assisted by the droplets of an appropriate organic solvent. Benzene, toluene, ethylbenzene, and o-xylene were used as target analytes. The main factors potentially affecting the microextraction such as the nature and the volume of organic solvent, polydimethylsiloxane (PDMS) swelling, extraction time, agitation, temperature, and salts were optimized. The method requires a very low consumption of organic solvent. The relative enrichment factor is in the range of 7.1-32.4 for extraction in the presence of dichloromethane at an optimum volume of 18 μL mL(-1) of aqueous sample. This enhancement over regular polydimethylsiloxane fiber is primarily the result of the fiber swelling and of a stable thin layer of organic solvent attached to the surface of the PDMS fiber. The limit of detection ranges from 0.02 to 0.65 ng mL(-1) for the target compounds using a 7-μm bonded polydimethylsiloxane coating and a flame ionization detector. The validity of this method is demonstrated by the analysis of a real waste water sample. © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  10. Validation of an Analytical Method for Determination of 13 priority polycyclic aromatic hydrocarbons in mineral water using dispersive liquid-liquid microextraction and GC-MS

    PubMed Central

    Sadeghi, Ramezan; Kobarfard, Farzad; Yazdanpanah, Hassan; Eslamizad, Samira; Bayat, Mitra

    2016-01-01

    Dispersive liquid-liquid microextraction (DLLME) combined with gas chromatography–mass spectrometry (GC–MS) was used for the extraction and determination of 13 polycyclic aromatic hydrocarbons (PAHs) in mineral water samples. In this procedure, the suitable combination of extraction solvent (500 µL chloroform) and disperser solvent (1000 µL acetone) were quickly injected into the water sample (10.00 mL) by Hamilton syringe. After centrifugation, 500 µL of the lower organic phase was dried under a gentle stream of nitrogen, re-dissolved in chloroform and injected into GC-MS. Chloroform and acetone were found to be the best extraction and disperser solvent, respectively. Validation of the method was performed using spiked calibration curves. The enrichment factor ranged from 93 to 129 and the recovery ranged from 71 to 90%. The linear ranges for all the PAHs were 0.10-2.80 ngmL-1. The relative standard deviations (RSDs) of PAHs in water by using anthracene-d10 as internal standard, were in the range of 4-11% for most of the analytes (n = 3). Limit of detection (LOD) for different PAHs were between 0.03 and 0.1 ngmL-1. The method was successfully applied for the analysis of PAHs in mineral water samples collected from Tehran. PMID:27610156

  11. Determination of hydroxylated metabolites of polycyclic aromatic hydrocarbons in sediment samples by combining subcritical water extraction and dispersive liquid-liquid microextraction with derivatization.

    PubMed

    Wang, Xiaowei; Lin, Li; Luan, Tiangang; Yang, Lihua; Tam, Nora F Y

    2012-11-13

    A sample preparation method for the determination of hydroxylated polycyclic aromatic hydrocarbons (OH-PAHs) in sediment samples was developed using gas chromatography-mass spectrometry (GC-MS). Dispersive liquid-liquid microextraction (DLLME) with derivatization was performed following the subcritical water extraction (SWE) that provided which was provided by accelerated solvent extraction (ASE). Several important parameters that affected both SWE extraction and DLLME, such as the selection of organic modifier, its volume, extraction temperature, extraction pressure and extraction time were also investigated. High sensitivity of the hydroxylated PAHs derivatives by N-(tert-butyldimethylsilyl)-N-methyl-trifluoroacetamide (MTBSTFA) could be achieved with the limits of detection (LODs) ranging from 0.0139 (2-OH-nap) to 0.2334 μg kg(-1) (3-OH-fluo) and the relative standard deviations (RSDs) between 2.81% (2-OH-phe) and 11.07% (1-OH-pyr). Moreover, the proposed method was compared with SWE coupled with solid phase extraction (SPE), and the results showed that ASE-DLLME was more promising with recoveries ranging from 57.63% to 91.07%. The proposed method was then applied to determine the hydroxylated metabolites of phenanthrene in contaminated sediments produced during the degradation by two PAH-degraders isolated from mangrove sediments.

  12. The accumulation of polycyclic aromatic hydrocarbons in lubricating oil over time--a comparison of supercritical fluid and liquid-liquid extraction methods.

    PubMed

    Wong, P K; Wang, J

    2001-01-01

    Optimal extraction conditions including extraction temperature, fluid density of carbon dioxide and concentration of modifier for supercritical fluid extraction (SFE) to extract of 16 2-6-ring polycyclic aromatic hydrocarbons (PAHs) spiked into used lubricating oil collected from a gasoline-driven automobile were determined. A comparison of extraction efficiency 2-6-ring PAHs spiked into the used lubricating oil extracted by SFE and liquid-liquid extraction (LLE) methods was made. Results indicated that recoveries of PAHs extracted by SFE from the used lubricating oil were higher than those by LLE. PAH profiles of lubricating oil samples collected at various driving distances from an old and a new gasoline-driven automobiles were determined by combining SFE, gel permeation chromatography clean up and gas chromatography-mass spectrometry analysis. Results showed that the concentrations of total PAH in lubricating oils collected from both automobiles increased rapidly after oil change. Two- and three-ring PAHs dominated the PAH profiles of oil samples collected from both automobiles. High concentrations of the more toxic 4-6-ring PAHs, were found in the oil samples collected from both automobiles even at a short driving distance after oil change. The concentrations of total PAH in lubricating oil collected from two automobiles driven for a longer distance after oil change were very similar.

  13. Rapid determination of polycyclic aromatic hydrocarbons in grilled meat using microwave-assisted extraction and dispersive liquid-liquid microextraction coupled to gas chromatography-mass spectrometry.

    PubMed

    Kamankesh, Marzieh; Mohammadi, Abdorreza; Hosseini, Hedayat; Modarres Tehrani, Zohreh

    2015-05-01

    A simple and rapid analytical tech nique for the simultaneous determination of 16 polycyclic aromatic hydrocarbons (PAHs) in grilled meat was developed using microwave-assisted extraction and dispersive liquid-liquid microextraction (MAE-DLLME) followed by gas chromatography-mass spectrometry (GC-MS). The effective parameters in DLLME process were optimized. Good linear relationships were obtained for 16 PAHs in a range of 1-200 ng g(-1), with a correlation coefficient (R(2)) higher than 0.98. Limits of detection and limits of quantification were 0.15-0.3 ng g(-1) and 0.47-1 ng g(-1), respectively. The relative standard deviations (RSD%) for seven analyses were less than 9%. The recoveries of those compounds in grilled meat were obtained from 85% to 104%. Low consumption of the solvent, high recovery, short extraction time, no matrix interference and good merit figures compared to other methods are advantages of the proposed method. The performance of the present method was evaluated for the determination of PAHs in various types of real grilled meat samples, and satisfactory results were obtained.

  14. Liquid-expanded-liquid-condensed phase transition in amphiphilic monolayers: A renormalization-group approach to chiral-symmetry breaking of hydrocarbon-chain defects

    NASA Astrophysics Data System (ADS)

    Legré, J.-P.; Albinet, G.; Firpo, J.-L.; Tremblay, A.-M. S.

    1984-11-01

    This paper is concerned with the liquid-expanded (LE) -liquid-condensed (LC) transition in monolayers of amphiphilic molecules at the air-water interface. A model, which can be mapped into the Blume-Emery-Griffiths Hamiltonian, has been considered before within the (mean-field) Bragg-Williams approximation and it gave results which could be successfully compared with experiment. The LE-LC transition has been associated with a chiral-symmetry breaking of the hydrocarbon-chain defects. This model is treated here with a Migdal-Kadanoff approximate position-space renormalization group. Renormalization-group flows are consistent with those obtained by previous authors. The connection between experimental and Hamiltonian parameters is easiest for a particular choice of ensemble, which turns out to be rather subtle for this problem. As in the work of Lavis, Southern, and Bell, isotherms in the surface-pressure-molecular-area plane do not show a signature of the LE-LC transition. The better agreement between experiments (showing a compressibility jump at the LE-LC transition) and mean-field theory suggests that in these cases long-range forces depending on the nature of the polar head and on the water substrate pH are responsible for the jump.

  15. Magnetic solid phase extraction using gold immobilized magnetic mesoporous silica nanoparticles coupled with dispersive liquid-liquid microextraction for determination of polycyclic aromatic hydrocarbons.

    PubMed

    Mehdinia, Ali; Khojasteh, Esmail; Baradaran Kayyal, Tohid; Jabbari, Ali

    2014-10-17

    An efficient magnetic sorbent was introduced for solid phase extraction by incorporation of the gold nanoparticles into the hexagonal lattice of magnetic MCM-41. For the effective incorporation of the gold nanoparticles, magnetic MCM-41 was functionalized with 3-aminopropyltriethoxysilane (APTES), which then interacted with Au atoms through the amine groups. Furthermore, to achieve high pre-concentration factors (PFs), the method was coupled with dispersive liquid-liquid microextraction (DLLME) procedure. Polycyclic aromatic hydrocarbons (PAHs) were used as the model compounds to evaluate the extraction performance of the proposed method. The π-system of PAH compounds and immobilized Au atoms on the surface of the sorbent can cause the electron donor-acceptor interactions. The parameters affecting extraction recovery such as types of the disperser and extraction solvents, pH of the sample solution, and the extraction time were optimized. Under the optimized conditions, the high PFs were obtained in the range 5519-6271 for the target analytes. The kinetic adsorption illustrated that 5 min was sufficient to achieve adsorption equilibrium for PAHs. The evaluations also showed a linearity range 0.01-50 μg L(-1) with the detection limit in the range 0.002-0.004 μg L(-1) for the PAHs. The applicability of the method for the analysis of PAHs in real samples was justified by the extraction of PAHs from seawater samples. The results indicated good recovery efficiencies ranging from 91.4 to 104.2%.

  16. Interim response action, basin F liquid incineration project. Draft final human health assessment. Volume 1

    SciTech Connect

    1993-09-02

    The multipathway human health risk assessment based on the SQ1 emission rates measured during the trial burn of basin F liquid indicates that the maximum level of human health risk associated with operation of this incinerator will not exceed the benchmark risk levels defined in the final decision document (Woodward-Clyde, 1990).

  17. Real-time prediction of hydrocarbon emissions from liquid combustion systems

    SciTech Connect

    Barton, R.G.; Riale, M.; McCampbell, D.; VanDyne, M.

    1997-12-31

    A laboratory study was conducted to investigate the ability of heuristic computational techniques to predict hydrocarbon emissions using data from simple process and optical monitors. A mini-pilot scale combustion research facility located at Midwest Research Institute was used was used in the study. The facility`s operational and emissions characteristics have been well defined in previous studies. The facility was fired with fuel oil and operated at wide range of combustion conditions. All operating parameters including fuel feed rate, air feed rates and chamber temperature were monitored. In addition, a CCD-array video camera was used to monitor the flame. An array of conventional continuous emissions monitors for CO, CO{sub 2}, O{sub 2}, and THC sampled the exhaust gases. The operational data and the optical field data were combined with the emissions data to form a training data set for a neural network. The trained network was then used to predict the THC emissions.

  18. Conversion of light hydrocarbon gases to metal carbides for production of liquid fuels and chemicals. Quarterly technical status report, October 1--December 31, 1992

    SciTech Connect

    Diaz, A.F.; Modestino, A.J.; Howard, J.B.; Peters, W.A.

    1993-02-01

    Light hydrocarbon gases could be reacted with low cost alkaline earth metal oxide (CaO, MgO) in high-temperature plasma reactor to achieve very high ({le}100%) gas conversion to H{sub 2}, CO, and the corresponding metal carbides. These carbides could be stored, transported, and hydrolyzed to acetylene or methyl acetylene, which in turn could be upgraded to a wide range of chemicals and premium liquid hydrocarbon fuels. An electric arc discharge reactor was built for converting methane. Literature reviews were made.

  19. The Separation and Identification of Straight Chain Hydrocarbons: An Experiment Using Gas-Liquid Chromatography.

    ERIC Educational Resources Information Center

    Benson, G. A.

    1982-01-01

    An experiment using gas-liquid chromatography is discussed, introducing the student to concept of dead volume and its measurement, idea and use of an internal reference compound, and to linear relationship existing between measurements of a separation on two different stationary phases. (Author/SK)

  20. LIGHT NONAQUEOUS-PHASE LIQUID HYDROCARBON WEATHERING AT SOME JP-4 FUEL RELEASE SITES

    EPA Science Inventory

    A fuel weathering study was conducted for database entries to estimate natural light, nonaqueousphase
    liquid weathering and source-term reduction rates for use in natural attenuation models. A range of BTEX
    weathering rates from mobile LNAPL plumes at eight field sites with...

  1. The Separation and Identification of Straight Chain Hydrocarbons: An Experiment Using Gas-Liquid Chromatography.

    ERIC Educational Resources Information Center

    Benson, G. A.

    1982-01-01

    An experiment using gas-liquid chromatography is discussed, introducing the student to concept of dead volume and its measurement, idea and use of an internal reference compound, and to linear relationship existing between measurements of a separation on two different stationary phases. (Author/SK)

  2. Portable kit for high-throughput analysis of polycyclic aromatic hydrocarbons using surface enhanced Raman scattering after dispersive liquid-liquid microextraction.

    PubMed

    Zhang, Min; Zhang, Xiaoli; Qu, Baofeng; Zhan, Jinhua

    2017-12-01

    In this work, a portable kit was developed for convenient high-throughput trace analysis of polycyclic aromatic hydrocarbons (PAHs) using surface enhanced Raman scattering (SERS) after dispersive liquid-liquid microextraction (DLLME) process. This portable kit contains three sealed reagent tubes (labeled as T1, T2 and T3), a self-made well plate, and a portable Raman spectrometer. The reagent tube T1 contains a mixture of disperser solvent and extraction solvent, which involved a 2min sample pretreatment of DLLME process. The quick injection of solvents in tube T1 into the sample containing PAHs formed a cloudy solution immediately, which consists of fine droplets of extraction solvent dispersed entirely into aqueous phase. The enrichment factor was found to be 29.6. T2 and T3 contain methanol and 1-propanethiol-modified silver nanoparticles (PTH-Ag NPs), respectively. The liquid in the tube T3 was used to enhance the Raman signal of analytes on the self-made high-throughput micro reactor. A linear relationship between the concentration of pyrene and the relative Raman peak intensity was obtained (R(2) = 0.993). The detection limit was 0.50μgL(-1) for pyrene. RSD of the high-throughput analysis of 12 samples was calculated as 4.8%. The ability of DLLME-SERS technique in the extraction of PAH isomers from water samples were investigated. The performance of DLLME-SERS in the recovery of pyrene from lake, spring and drinking water was also studied. Copyright © 2017 Elsevier B.V. All rights reserved.

  3. Dielectric loss of liquid hydrocarbons in the millimetre and submillimetre wavelength regions

    NASA Astrophysics Data System (ADS)

    Richter, W.; Schiel, D.

    1984-05-01

    The dielectric-loss tangent of liquid cyclohexane, n-hexane, n-heptane and n-octane has been determined in the frequency range 4-300 cm -1 (120 GHz-9 THz) by means of power absorption measurements using rapid-scan FTS. The results agree with literature data for cyclohexane obtained with dispersive FTS and link up well with existing microwave results, corroborating the existence of a low-frequency dielectric-loss maximum with the n-alkanes. The origin of the dielectric loss of these low-loss liquids is considered to be due to relaxational processes of weak permanent dipoles and low-lying intramolecular vibrations in the case of the n-alkanes, and to interaction-induced absorption in the case of cyclohexane.

  4. On the Extraction of Aromatic Compounds from Hydrocarbons by Imidazolium Ionic Liquids

    PubMed Central

    Cassol, Cláudia C.; Umpierre, Alexandre P.; Ebeling, Günter; Ferrera, Bauer; Chiaro, Sandra S. X.; Dupont, Jairton

    2007-01-01

    The liquid-liquid equilibrium for the ternary system formed by n-octane and aromatic (alkylbenzenes) and heteroaromatic compounds (nitrogen and sulfur containing heterocyles) and 1-alkyl-3-methylimidazolium ionic liquids (ILs) associated with various anions has been investigated. The selectivity on the extraction of a specific aromatic compound is influenced by anion volume, hydrogen bond strength between the anion and the imidazolium cation and the length of the 1-methyl-3-alkylimidazolium alkyl side chain. The interaction of alkylbenzenes and sulfur heterocyles with the IL is preferentially through CH-π hydrogen bonds and the quantity of these aromatics in the IL phase decreases with the increase of the steric hindrance imposed by the substituents on the aromatic nucleus. In the case of nitrogen heterocycles the interaction occurs preferentially through N(heteroaromatic)-H(imidazolium) hydrogen bonds and the extraction process is largely controlled by the nitrogen heterocycle pKa. Competitive extraction experiments suggest that benzene, pyridine and dibenzothiophene do not compete for the same hydrogen bond sites of the IL.

  5. Hydrocarbon Liquid Production via Catalytic Hydroprocessing of Phenolic Oils Fractionated from Fast Pyrolysis of Red Oak and Corn Stover

    SciTech Connect

    Elliott, Douglas C.; Wang, Huamin; Rover, Majorie; Whitmer, Lysle; Smith, Ryan; Brown, Robert C.

    2015-04-13

    Phenolic oils were produced from fast pyrolysis of two different biomass feedstocks, red oak and corn stover and evaluated in hydroprocessing tests for production of liquid hydrocarbon products. The phenolic oils were produced with a bio-oil fractionating process in combination with a simple water wash of the heavy ends from the fractionating process. Phenolic oils derived from the pyrolysis of red oak and corn stover were recovered with yields (wet biomass basis) of 28.7 wt% and 14.9 wt%, respectively, and 54.3% and 58.6% on a carbon basis. Both precious metal catalysts and sulfided base metal catalyst were evaluated for hydrotreating the phenolic oils, as an extrapolation from whole bio-oil hydrotreatment. They were effective in removing heteroatoms with carbon yields as high as 81% (unadjusted for the 90% carbon balance). There was nearly complete heteroatom removal with residual O of only 0.4% to 5%, while N and S were reduced to less than 0.05%. Use of the precious metal catalysts resulted in more saturated products less completely hydrotreated compared to the sulfided base metal catalyst, which was operated at higher temperature. The liquid product was 42-52% gasoline range molecules and about 43% diesel range molecules. Particulate matter in the phenolic oils complicated operation of the reactors, causing plugging in the fixed-beds especially for the corn stover phenolic oil. This difficulty contrasts with the catalyst bed fouling and plugging, which is typically seen with hydrotreatment of whole bio-oil. This problem was substantially alleviated by filtering the phenolic oils before hydrotreating. More thorough washing of the phenolic oils during their preparation from the heavy ends of bio-oil or on-line filtration of pyrolysis vapors to remove particulate matter before condensation of the bio-oil fractions is recommended.

  6. Hydrocarbon Liquid Production via Catalytic Hydroprocessing of Phenolic Oils Fractionated from Fast Pyrolysis of Red Oak and Corn Stover

    DOE PAGES

    Elliott, Douglas C.; Wang, Huamin; Rover, Majorie; ...

    2015-04-13

    Phenolic oils were produced from fast pyrolysis of two different biomass feedstocks, red oak and corn stover and evaluated in hydroprocessing tests for production of liquid hydrocarbon products. The phenolic oils were produced with a bio-oil fractionating process in combination with a simple water wash of the heavy ends from the fractionating process. Phenolic oils derived from the pyrolysis of red oak and corn stover were recovered with yields (wet biomass basis) of 28.7 wt% and 14.9 wt%, respectively, and 54.3% and 58.6% on a carbon basis. Both precious metal catalysts and sulfided base metal catalyst were evaluated for hydrotreatingmore » the phenolic oils, as an extrapolation from whole bio-oil hydrotreatment. They were effective in removing heteroatoms with carbon yields as high as 81% (unadjusted for the 90% carbon balance). There was nearly complete heteroatom removal with residual O of only 0.4% to 5%, while N and S were reduced to less than 0.05%. Use of the precious metal catalysts resulted in more saturated products less completely hydrotreated compared to the sulfided base metal catalyst, which was operated at higher temperature. The liquid product was 42-52% gasoline range molecules and about 43% diesel range molecules. Particulate matter in the phenolic oils complicated operation of the reactors, causing plugging in the fixed-beds especially for the corn stover phenolic oil. This difficulty contrasts with the catalyst bed fouling and plugging, which is typically seen with hydrotreatment of whole bio-oil. This problem was substantially alleviated by filtering the phenolic oils before hydrotreating. More thorough washing of the phenolic oils during their preparation from the heavy ends of bio-oil or on-line filtration of pyrolysis vapors to remove particulate matter before condensation of the bio-oil fractions is recommended.« less

  7. Hydrocarbon Liquid Production from Biomass via Hot-Vapor-Filtered Fast Pyrolysis and Catalytic Hydroprocessing of the Bio-oil

    SciTech Connect

    Elliott, Douglas C.; Wang, Huamin; French, Richard; Deutch, Steve; Iisa, Kristiina

    2014-08-14

    Hot-vapor filtered bio-oils were produced from two different biomass feedstocks, oak and switchgrass, and the oils were evaluated in hydroprocessing tests for production of liquid hydrocarbon products. Hot-vapor filtering reduced bio-oil yields and increased gas yields. The yields of fuel carbon as bio-oil were reduced by ten percentage points by hot-vapor filtering for both feedstocks. The unfiltered bio-oils were evaluated alongside the filtered bio-oils using a fixed bed catalytic hydrotreating test. These tests showed good processing results using a two-stage catalytic hydroprocessing strategy. Equal-sized catalyst beds, a sulfided Ru on carbon catalyst bed operated at 220°C and a sulfided CoMo on alumina catalyst bed operated at 400°C were used with the entire reactor at 100 atm operating pressure. The products from the four tests were similar. The light oil phase product was fully hydrotreated so that nitrogen and sulfur were below the level of detection, while the residual oxygen ranged from 0.3 to 2.0%. The density of the products varied from 0.80 g/ml up to 0.86 g/ml over the period of the test with a correlated change of the hydrogen to carbon atomic ratio from 1.79 down to 1.57, suggesting some loss of catalyst activity through the test. These tests provided the data needed to assess the suite of liquid fuel products from the process and the activity of the catalyst in relationship to the existing catalyst lifetime barrier for the technology.

  8. Emulsification liquid-liquid microextraction based on deep eutectic solvent: An extraction method for the determination of benzene, toluene, ethylbenzene and seven polycyclic aromatic hydrocarbons from water samples.

    PubMed

    Khezeli, Tahere; Daneshfar, Ali; Sahraei, Reza

    2015-12-18

    In this study, for the first time, a simple, inexpensive and sensitive method named emulsification liquid-liquid microextraction based on deep eutectic solvent (ELLME-DES) was used for the extraction of benzene, toluene, ethylbenzene (BTE) and seven polycyclic aromatic hydrocarbons (PAHs) from water samples. In a typical experiment, 100μL of DES (as water-miscible extraction solvent) was added to 1.5mL of sample solution containing target analytes. A homogeneous solution was formed immediately. Injection of 100μL of THF (as emulsifier agent) into homogeneous solution provided a turbid state. After extraction, phase separation (aqueous phase/DES rich phase) was performed by centrifugation. DES rich phase was withdrawn by a micro-syringe and submitted to isocratic reverse-phase HPLC with UV detection. Under optimum conditions obtained by response surface methodology (RSM) and desirability function (DF), the calibration graphs were linear in the concentration range from 10 to 200μg/L for benzene, 10-400μg/L for toluene, 1-400μg/L for ethylbenzene, biphenyl, chrysene and fluorene, and 0.1-400μg/L for anthracene, benzo[a]pyrene, phenanthrene and pyrene. The coefficients of determination (r(2)) and limits of detection were 0.9924-0.9997 and 0.02-6.8μg/L, respectively. This procedure was successfully applied to the determination of target analytes in spiked water samples. The relative mean recoveries ranged from 93.1 to 103.3%.

  9. [Low-density solvent-based solvent demulsification dispersive liquid-liquid microextraction combined with gas chromatography for determination of polycyclic aromatic hydrocarbons in water samples].

    PubMed

    Zhu, Benqiong; Chen, Hao; Li, Shengqing

    2012-02-01

    A novel method of low-density solvent-based solvent demulsification dispersive liquid-liquid microextraction (SD-DLLME) was developed for the determination of eight polycyclic aromatic hydrocarbons (PAHs) in water samples by gas chromatography-flame ionization detection (GC-FID). Conventional DLLME methods usually employ organic solvents heavier than water as the extraction solvents and achieve the phase separation through centrifugation. On the contrary, in this proposed extraction procedure, a mixture of low-density extraction solvent (toluene) and dispersive solvent (acetone) was injected into the aqueous sample solution to form an emulsion. A demulsification solvent (acetonitrile) was then injected into the aqueous solution to break up the emulsion, which turned clear quickly and was separated into two layers. The upper layer (toluene) was collected and analyzed by GC. No centrifugation was required in this procedure. Factors affecting the extraction efficiency such as the type and volume of dispersive solvent, extraction solvent and de-emulsifier were investigated in detail. Under the optimized conditions, the proposed method provided a good linearity in the range of 20 - 500 microg/L (r2 = 0.994 2 - 0.999 9). The limits of detection (S/N = 3) were in the range of 0.52 - 5.11 microg/L. The relative standard deviations (RSDs) for the determination of 40 microg/L PAHs were in the range of 2.2% - 13.6% (n = 5). The proposed method is fast, efficient and convenient. It has been successfully applied to the determination of PAHs in natural water samples with the spiked recoveries of 80.2% - 115.1%.

  10. Ionization in liquids. Final technical report, November 1, 1993--December 31, 1995

    SciTech Connect

    Bakale, G.

    1996-03-29

    The objective of these studies which began in 1993 was to provide new information on electron and ion transport and reactions in model liquids and biomimetic systems that is pertinent to the roles of charged species in inducing radiobiological damage and to elucidate the interrelationship among the carcinogenicity, mutagenicity and electrophilicity of chemicals. This final report summarizes research efforts in the following areas: electrons in biological systems; and electron and ion transport and reactions in model liquids. In biological systems attention was focused on the following: excess electrons as probes of carcinogen electrophilicity; cost effectiveness of k{sub e} as a carcinogen-screening test; and conversion of k{sub e} to a carcinogen-screening electronic device. In model liquids, research was focused on two areas. The first investigated radiation-induced dimerization of fullerenes. The second area studied radiolytic synthesis of fullerene derivatives.

  11. Development of a wet vapor homogeneous liquid metal MHD power system. Final report

    SciTech Connect

    Branover, H.; Unger, Y.; El-Boher, A.; Schweitzer, H.

    1991-09-01

    A feasibility study for the approval of liquid metal seeds recovery from a liquid metal vapor-inert gas mixture was conducted and presented in this report. The research activity included background studies on processes relating to mixing stream condenser performance, parametric studies and its experimental validation. The condensation process under study includes mass transfer phenomena combined with heat transfer and phase change. Numerical methods were used in order to solve the dynamic equations and to carry out the parametric study as well as the experimental data reduction. The MSC performance is highly effected by droplet diameter, thus the possibility of atomizing liquid metals were experimentally investigated. The results are generalized and finally used for a set of recommendations by which the recovery of seeds is expected to be feasible.

  12. On-line flow injection-cloud point preconcentration of polycyclic aromatic hydrocarbons coupled with high-performance liquid chromatography.

    PubMed

    Li, Cheuk Fai; Wong, Jonathan W C; Huie, Carmen W; Choi, Martin M F

    2008-12-19

    Cloud point methodology has been used to develop a novel preconcentration and an analytical method for polycyclic aromatic hydrocarbons (PAHs) in soil sample. The nonionic surfactant Tergitol 15-S-7 was successfully used as the surfactant-mediated extractant in both ultrasonic and microwave-assisted extractions. Over 90% of recoveries for various PAHs in soil were obtained under the optimal experimental conditions. The extracts were then preconcentrated and analyzed by our proposed on-line coupling method "flow injection-cloud point preconcentration-high-performance liquid chromatography" (FI-CPP-HPLC) equipped with a fluorescence detector and an excitation/emission wavelength program. The preconcentration system and optimal working conditions were established. The limit of detection of the FI-CPE-HPLC system ranges from 0.101 to 0.456 microg/L for the selected PAHs, i.e., phenanthrene, pyrene, chrysene, benzo[k]fluoranthene and benzo[a]pyrene. Our proposed technique provides a reliable, simple and automatic analytical method for the determination of PAHs in environmental soil samples.

  13. Extracellular polymeric substances enhanced mass transfer of polycyclic aromatic hydrocarbons in the two-liquid-phase system for biodegradation.

    PubMed

    Zhang, Yinping; Wang, Fang; Yang, Xinglun; Gu, Chenggang; Kengara, Fredrick Orori; Hong, Qing; Lv, Zhengyong; Jiang, Xin

    2011-05-01

    The objective was to elucidate the role of extracellular polymeric substances (EPS) in biodegradation of polycyclic aromatic hydrocarbons in two-liquid-phase system (TLPs). Therefore, biodegradation of phenanthrene (PHE) was conducted in a typical TLPs--silicone oil-water--with PHE-degrading bacteria capable of producing EPS, Sphingobium sp. PHE3 and Micrococcus sp. PHE9. The results showed that the presence of both strains enhanced mass transfer of PHE from silicone oil to water, and that biodegradation of PHE mainly occurred at the interfaces. The ratios of tightly bound (TB) proteins to TB polysaccharides kept almost constant, whereas the ratios of loosely bound (LB) proteins to LB polysaccharides increased during the biodegradation. Furthermore, polysaccharides led to increased PHE solubility in the bulk water, which resulted in an increased PHE mass transfer. Both LB-EPS and TB-EPS (proteins and polysaccharides) correlated with PHE mass transfer in silicone oil, indicating that both proteins and polysaccharides favored bacterial uptake of PHE at the interfaces. It could be concluded that EPS could facilitate microbial degradation of PHE in the TLPs.

  14. Ultra-high performance liquid chromatographic method for the determination of polycyclic aromatic hydrocarbons in a passive environmental sampler.

    PubMed

    Purcaro, Giorgia; Moret, Sabrina; Bučar-Miklavčič, Milena; Conte, Lanfranco S

    2012-04-01

    Polycyclic aromatic hydrocarbons (PAHs) are ubiquitous compounds released in the environment by different sources. The aim of the present work was to validate a solid-phase extraction (SPE) and a rapid ultra-high performance liquid chromatographic (UHPLC) method for the analysis of PAHs in a passive environmental sampler, namely a Dacron® (the commercial name of a synthetic fiber based on polyethylene terephthalate) textile. The elution temperature was optimized to improve the resolution of early-eluted compounds, namely acenaphthene (Ac) and fluorene (F). The UHPLC method lasts about 10 min and showed good linearity for all the 16 PAHs considered, with regression coefficients over 0.99. Recoveries, limits of detection (LODs), and limits of quantification (LOQs) of the SPE method were well within the performance criteria fixed by the Regulation n. 836/2011, namely 0.3 and 0.9 μg/kg, respectively. © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  15. Determination of polycyclic aromatic hydrocarbons in fresh milk by hollow fiber liquid-phase microextraction-gas chromatography mass spectrometry.

    PubMed

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

    2013-02-01

    In this work, a two-phase hollow fiber liquid-phase microextraction (HF-LPME) method combined with gas chromatography-mass spectrometry (GC-MS) is developed to provide a rapid, selective and sensitive analytical method to determine polycyclic aromatic hydrocarbons (PAHs) in fresh milk. The standard addition method is used to construct calibration curves and to determine the residue levels for the target analytes, fluorene, phenanthrene, fluoranthene, pyrene and benzo[a]pyrene, thus eliminating sample pre-treatment steps such as pH adjustment. The HF-LPME method shows dynamic linearity from 5 to 500 µg/L for all target analytes with R(2) ranging from 0.9978 to 0.9999. Under optimized conditions, the established detection limits range from 0.07 to 1.4 µg/L based on a signal-to-noise ratio of 3:1. Average relative recoveries for the determination of PAHs studied at 100 µg/L spiking levels are in the range of 85 to 110%. The relative recoveries are slightly higher than those obtained by conventional solvent extraction, which requires saponification steps for fluorene and phenanthrene, which are more volatile and heat sensitive. The HF-LPME method proves to be simple and rapid, and requires minimal amounts of organic solvent that supports green analysis.

  16. Contribution of power and desalination plants to the levels of volatile liquid hydrocarbons in the nearby coastal areas of Kuwait

    SciTech Connect

    Saeed, T.; Khordagui, H.; Al-Hashash, H.

    1999-07-01

    The levels and distribution of volatile liquid hydrocarbons (VLHs) were determined in Kuwait`s coastal areas in the vicinity of outlets of power and desalination plants. About 230 samples were collected from the selected sampling locations over the 4 seasons. The VLHs in the samples were analyzed using Grob`s closed-loop stripping technique and GC with FID and confirmed by GC/MS. The results showed that significant levels of VLHs were present. The levels ranged from 307 to 6,500 ng/L and from 2,880 to 7,811 ng/L in Kuwait Bay and Sulaibekhat Bay, respectively. The annual average for VLHs near Al-Zor power plant ranged from 465 to 4,665 ng/L. Benzenoids formed the bulk (about 80%) of the VLHs present. Comparison with the levels in the outlets indicated that Doha West power plant contributed much higher levels of VLHs to the coastal areas than Al-Zor plant.

  17. Determination of polycyclic aromatic hydrocarbons in drinking water samples by solid-phase nanoextraction and high-performance liquid chromatography.

    PubMed

    Wang, Huiyong; Campiglia, Andres D

    2008-11-01

    A novel alternative is presented for the extraction and preconcentration of polycyclic aromatic hydrocarbons (PAH) from water samples. The new approachwhich we have named solid-phase nanoextraction (SPNE)takes advantage of the strong affinity that exists between PAH and gold nanoparticles. Carefully optimization of experimental parameters has led to a high-performance liquid chromatography method with excellent analytical figures of merit. Its most striking feature correlates to the small volume of water sample (500 microL) for complete PAH analyses. The limits of detection ranged from 0.9 (anthracene) to 58 ng.L (-1) (fluorene). The relative standard deviations at medium calibration concentrations vary from 3.2 (acenaphthene) to 9.1% (naphthalene). The analytical recoveries from tap water samples of the six regulated PAH varied from 83.3 +/- 2.4 (benzo[ k]fluoranthene) to 95.7 +/- 4.1% (benzo[ g,h,i]perylene). The entire extraction procedure consumes less than 100 microL of organic solvents per sample, which makes it environmentally friendly. The small volume of extracting solution makes SPNE a relatively inexpensive extraction approach.

  18. Development of a Comprehensive and Predictive Reaction Mechanism of Liquid Hydrocarbon Combustion

    DTIC Science & Technology

    2007-01-01

    30-01-2007 Final Technical Report 1111/2004- 10/3112006 4 . TITLE AND SUBTITLE 5a. CONTRACT NUMBER 53-4514-0001 DEVELOPMENT OF A COMPREHENSIVE AND...ACRONYM(S) Air Force Office of Scientific Research 875 North Randolph Street, Suite 325 Arlington, VA 22203 11. SPONSOR/MONITOR’S REPORT )(- r 4 -Qt -- /1...radical, (3) a theoretical kinetic study of the decomposition of ethylene oxide; ( 4 ) a gas-kinetic analysis for the transport properties of long chain

  19. Hydrocarbon-Seeded Ignition System for Small Spacecraft Thrusters Using Ionic Liquid Propellants

    NASA Technical Reports Server (NTRS)

    Whitmore, Stephen A.; Merkley, Daniel P.; Eilers, Shannon D.; Taylor, Terry L.

    2013-01-01

    "Green" propellants based on Ionic-liquids (ILs) like Ammonium DiNitramide and Hydroxyl Ammonium Nitrate have recently been developed as reduced-hazard replacements for hydrazine. Compared to hydrazine, ILs offer up to a 50% improvement in available density-specific impulse. These materials present minimal vapor hazard at room temperature, and this property makes IL's potentially advantageous for "ride-share" launch opportunities where hazards introduced by hydrazine servicing are cost-prohibitive. Even though ILs present a reduced hazard compared to hydrazine, in crystalline form they are potentially explosive and are mixed in aqueous solutions to buffer against explosion. Unfortunately, the high water content makes IL-propellants difficult to ignite and currently a reliable "coldstart" capability does not exist. For reliable ignition, IL-propellants catalyst beds must be pre-heated to greater than 350 C before firing. The required preheat power source is substantial and presents a significant disadvantage for SmallSats where power budgets are extremely limited. Design and development of a "micro-hybrid" igniter designed to act as a "drop-in" replacement for existing IL catalyst beds is presented. The design requires significantly lower input energy and offers a smaller overall form factor. Unlike single-use "squib" pyrotechnic igniters, the system allows the gas generation cycle to be terminated and reinitiated on demand.

  20. Liquid oxygen cooling of high pressure LOX/hydrocarbon rocket thrust chambers

    NASA Technical Reports Server (NTRS)

    Price, H. G.; Masters, P. A.

    1986-01-01

    An experimental program using liquid oxygen (LOX) and RP-1 as the propellants and supercritical LOX as the coolant was conducted at 4.14, 8.27, and 13.79 MN/sq m (600, 1200, and 2000 psia) chamber pressure. The objectives of this program were to evaluate the cooling characteristics of LOX with the LOX/RP-1 propellants, the buildup of the soot on the hot-gas-side chamber wall, and the effect of an internal LOX leak on the structural integrity of the combustor. Five thrust chambers with throat diameters of 6.6 cm (2.5 in.) were tested successfully. The first three were tested at 4.14 MN/sq m (600 psia) chamber pressure over a mixture ratio range of 2.25 to 2.92. One of these three was tested for over 22 cyclic tests after the first through crack from the coolant channel to the combustion zone was observed with no apparent metal burning or distress. The fourth chamber was tested at 8.27 MN/sq m (1200 psia) chamber pressure over a mixture range of 1.93 to 2.98. The fourth and fifth chambers were tested at 13.79 MN/sq m (2000 psia) chamber pressure over a mixture ratio range of 1.79 to 2.68.

  1. Group-type hydrocarbon standards for high-performance liquid chromatographic analysis of middistillate fuels

    NASA Technical Reports Server (NTRS)

    Otterson, D. A.; Seng, G. T.

    1984-01-01

    A new high-performance liquid chromatographic (HPLC) method for group-type analysis of middistillate fuels is described. It uses a refractive index detector and standards that are prepared by reacting a portion of the fuel sample with sulfuric acid. A complete analysis of a middistillate fuel for saturates and aromatics (including the preparation of the standard) requires about 15 min if standards for several fuels are prepared simultaneously. From model fuel studies, the method was found to be accurate to within 0.4 vol% saturates or aromatics, and provides a precision of + or - 0.4 vol%. Olefin determinations require an additional 15 min of analysis time. However, this determination is needed only for those fuels displaying a significant olefin response at 200 nm (obtained routinely during the saturated/aromatics analysis procedure). The olefin determination uses the responses of the olefins and the corresponding saturates, as well as the average value of their refractive index sensitivity ratios (1.1). Studied indicated that, although the relative error in the olefins result could reach 10 percent by using this average sensitivity ratio, it was 5 percent for the fuels used in this study. Olefin concentrations as low as 0.1 vol% have been determined using this method.

  2. A novel concept for high conversion of coal to liquids. Final report, 1 September 1988--31 August 1992

    SciTech Connect

    Wiser, W.H.; Shabtai, J.

    1994-04-01

    A batch microreactor was designed and fabricated as a means of investigating maximum yields of liquids obtainable in very short reaction times of the order of a few seconds, and the maximum ratios of liquids/hydrocarbon (HC) gases obtainable under those conditions. A Wyodak sub-bituminous coal, crushed and sieved to {minus}200 mesh particle size, was used in the experiments, with a temperature of 500{degrees}C and a pressure of 1500 psi. The fine coal particles were fed dry to the reactor and heated to reaction temperature in times of one to two seconds. At a time of 3 seconds at reaction temperature, in a single pass a liquid yield of 60% by weight of the coal was obtained, accompanied by a ratio of liquids/(HC) gases of 30/1. When the unreacted solids were recycled to the reactor, and the results combined with those of the first pass, a liquid yield of 82% by weight of the coal was achieved, accompanied by a ratio of liquids/HC gases of 30/1. This ratio represents only about 3 wt percent HC gases, much lower that is produced in current advanced technologies, and represents a large saving in hydrogen consumption. A simulated distillation technique was applied to the liquids. The liquid product contained 86% by weight (of the liquids) total distillables (boiling point below 538{degrees}C), including 70% by weight of low-boiling fractions in the gasoline, kerosene and gas oil range (boiling point up to 325{degrees}C). The liquid product exhibited a H/C ratio of 1.5, which is considerably higher than observed in current advanced technologies for the primary liquids. Several catalysts were investigated. Iron catalysts, specifically ferric chloride hexahydrate and ferric sulfate pentahydrate, each produced these high conversions and high ratios of liquids/HC gases.

  3. Ultrasound-assisted oxidative desulfurization and denitrogenation of liquid hydrocarbon fuels: A critical review.

    PubMed

    Ja'fari, Mahsa; Ebrahimi, Seyedeh Leila; Khosravi-Nikou, Mohammad Reza

    2018-01-01

    Nowadays, a continuously worldwide concern for development of process to produce ultra-low sulfur and nitrogen fuels have been emerged. Typical hydrodesulfurization and hydrodenitrogenation technology deals with important difficulties such as high pressure and temperature operating condition, failure to treat some recalcitrant compounds and limitations to meet the stringent environmental regulations. In contrary an advanced oxidation process that is ultrasound assisted oxidative desulfurization and denitrogenation satisfies latest environmental regulations in much milder conditions with more efficiency. The present work deals with a comprehensive review on findings and development in the ultrasound assisted oxidative desulfurization and denitrogenation (UAOD) during the last decades. The role of individual parameters namely temperature, residence time, ultrasound power and frequency, pH, initial concentration and types of sulfur and nitrogen compounds on the efficiency are described. What's more another treatment properties that is role of phase transfer agent (PTA) and solvents of extraction step, reaction kinetics, mechanism of the ultrasound, fuel properties and recovery in UAOD are reviewed. Finally, the required future works to mature this technology are suggested. Copyright © 2017 Elsevier B.V. All rights reserved.

  4. Lipidic ionic liquid stationary phases for the separation of aliphatic hydrocarbons by comprehensive two-dimensional gas chromatography.

    PubMed

    Nan, He; Zhang, Cheng; O'Brien, Richard A; Benchea, Adela; Davis, James H; Anderson, Jared L

    2017-01-20

    Lipidic ionic liquids (ILs) possessing long alkyl chains as well as low melting points have the potential to provide unique selectivity as well as wide operating ranges when used as stationary phases in gas chromatography. In this study, a total of eleven lipidic ILs containing various structural features (i.e., double bonds, linear thioether chains, and cyclopropanyl groups) were examined as stationary phases in comprehensive two dimensional gas chromatography (GC×GC) for the separation of nonpolar analytes in kerosene. N-alkyl-N'-methyl-imidazolium-based ILs containing different alkyl side chains were used as model structures to investigate the effects of alkyl moieties with different structural features on the selectivities and operating temperature ranges of the IL-based stationary phases. Compared to a homologous series of ILs containing saturated side chains, lipidic ILs exhibit improved selectivity toward the aliphatic hydrocarbons in kerosene. The palmitoleyl IL provided the highest selectivity compared to all other lipidic ILs as well as the commercial SUPELCOWAX 10 column. The linoleyl IL containing two double bonds within the alkyl side chain showed the lowest chromatographic selectivity. The lipidic IL possessing a cyclopropanyl group within the alkyl moiety exhibited the highest thermal stability. The Abraham solvation parameter model was used to evaluate the solvation properties of the lipidic ILs. This study provides the first comprehensive examination into the relation between lipidic IL structure and the resulting solvation characteristics. Furthermore, these results establish a basis for applying lipidic ILs as stationary phases for solute specific separations in GC×GC. Copyright © 2016 Elsevier B.V. All rights reserved.

  5. New Mexico cloud super cooled liquid water survey final report 2009.

    SciTech Connect

    Beavis, Nick; Roskovensky, John K.; Ivey, Mark D.

    2010-02-01

    Los Alamos and Sandia National Laboratories are partners in an effort to survey the super-cooled liquid water in clouds over the state of New Mexico in a project sponsored by the New Mexico Small Business Assistance Program. This report summarizes the scientific work performed at Sandia National Laboratories during the 2009. In this second year of the project a practical methodology for estimating cloud super-cooled liquid water was created. This was accomplished through the analysis of certain MODIS sensor satellite derived cloud products and vetted parameterizations techniques. A software code was developed to analyze multiple cases automatically. The eighty-one storm events identified in the previous year effort from 2006-2007 were again the focus. Six derived MODIS products were obtained first through careful MODIS image evaluation. Both cloud and clear-sky properties from this dataset were determined over New Mexico. Sensitivity studies were performed that identified the parameters which most influenced the estimation of cloud super-cooled liquid water. Limited validation was undertaken to ensure the soundness of the cloud super-cooled estimates. Finally, a path forward was formulized to insure the successful completion of the initial scientific goals which include analyzing different of annual datasets, validation of the developed algorithm, and the creation of a user-friendly and interactive tool for estimating cloud super-cooled liquid water.

  6. Direct catalytic conversion of methane and light hydrocarbon gases. Final report, October 1, 1986--July 31, 1989

    SciTech Connect

    Wilson, R.B. Jr.; Posin, B.M.; Chan, Yee-Wai

    1995-06-01

    This project explored conversion of methane to useful products by two techniques that do not involve oxidative coupling. The first approach was direct catalytic dehydrocoupling of methane to give hydrocarbons and hydrogen. The second approach was oxidation of methane to methanol by using heterogenized versions of catalysts that were developed as homogeneous models of cytochrome-P450, an enzyme that actively hydroxylates hydrocarbons by using molecular oxygen. Two possibilities exist for dehydrocoupling of methane to higher hydrocarbons: The first, oxidative coupling to ethane/ethylene and water, is the subject of intense current interest. Nonoxidative coupling to higher hydrocarbons and hydrogen is endothermic, but in the absence of coke formation the theoretical thermodynamic equilibrium yield of hydrocarbons varies from 25% at 827{degrees}C to 65% at 1100{degrees}C (at atmospheric pressure). In this project we synthesized novel, highly dispersed metal catalysts by attaching metal clusters to inorganic supports. The second approach mimics microbial metabolism of methane to produce methanol. The methane mono-oxygenase enzyme responsible for the oxidation of methane to methanol in biological systems has exceptional selectivity and very good rates. Enzyme mimics are systems that function as the enzymes do but overcome the problems of slow rates and poor stability. Most of that effort has focused on mimics of cytochrome P-450, which is a very active selective oxidation enzyme and has a metalloporphyrin at the active site. The interest in nonporphyrin mimics coincides with the interest in methane mono-oxygenase, whose active site has been identified as a {mu}-oxo dinuclear iron complex.We employed mimics of cytochrome P-450, heterogenized to provide additional stability. The oxidation of methane with molecular oxygen was investigated in a fixed-bed, down-flow reactor with various anchored metal phthalocyanines (PC) and porphyrins (TPP) as the catalysts.

  7. Deashing of coal liquids with ceramic membrane microfiltration and diafiltration. Final technical report, August 4, 1992--September 30, 1995

    SciTech Connect

    1996-03-01

    Removal of mineral matter from liquid hydrocarbons derived from the direct liquefaction of coal is required for product acceptability. Current methods include critical solvent Deashing and filtration, both of which produce an ash reject stream containing up to 15% of the liquid hydrocarbon product. This program was directed towards development of an improved process for deashing and recovery of coal-derived residual oil: the use of ceramic membranes for high-temperature microfiltration and diafiltration. Using laboratory scale ceramic membrane modules, samples of a coal-derived residual oil containing ash were processed by crossflow microfiltration, followed by solvent addition and refiltration (diafiltration). Excellent recovery of deashed residual oil was demonstrated. Data from this program were used to develop preliminary estimates for production system capital and operating costs that will be used to assess economic feasibility. The first objective of this program was to demonstrate technical feasibility of crossflow microfiltration (MF) for removal of mineral matter from a coal derived residual oil. A second objective was to demonstrate technical feasibility of diafiltration of W concentrate using a hydrocarbon diluent.

  8. A molecular dynamics investigation into the adsorption behavior inside {001} kaolinite and {1014} calcite nano-scale channels: the case with confined hydrocarbon liquid, acid gases, and water

    NASA Astrophysics Data System (ADS)

    Fazelabdolabadi, Babak; Alizadeh-Mojarad, Aliasghar

    2017-06-01

    A set of molecular dynamics simulations was conducted, as the first comparative study of the adsorption behavior of liquid hydrocarbon/acid gases/water molecules over { 10\\bar{1}4} calcite surface and {001} octahedral kaolinite surface in nano-confined slit. According to atomic z-density profiles, hydrocarbon molecules have higher tendency towards the { 10\\bar{1}4} calcite surface than the {001} octahedral kaolinite surface. In addition, water molecules form stronger adsorption layer over calcite surface than kaolinite. In contrast, acid gas molecules have higher tendency towards kaolinite surface than calcite. This behavior was spotted within nanometer-sized slit pores. The results also point to reduction in self-diffusion coefficient of molecules with strong adsorption over mineral surfaces in nano-confined environment.

  9. Interim Response Action Basin F Liquid Incineration Project Final Draft Human Health Risk Assessment. Volume 1.

    DTIC Science & Technology

    1991-07-01

    91222R02 2ND COPY Interim Response Action Basin F Liquid Incineration Project FINAL DRAFT HUMAN HEALTH RISK ASSESSMENT V olumne I Preplaced Remedial...The Use of OELs and NAAQSs for Calculating Inhalation RfJ)s 9-13 9.4.2.2 Adjustments to Inhalation RfDs 9-14 793C/FM V 7/22/91 TABLE OF CONTENTS...HENDERSON RTHOL THOL HAZELTIN A I LE-- f V , Rocky Mountain WELB DA Arsenal A"ADA AA -AIL- VIM IT RUM Doi T p- 0 Denver kl& MOR SHER DAN r go, "- V

  10. Evaluation of the potential use of microorganisms in the cleanup of petroleum hydrocarbon spills in soils. Final report

    SciTech Connect

    Gunnison, D.

    1991-09-01

    Soils and sediments at many military facilities have been contaminated with petroleum hydrocarbons (gasoline, lubricating oil, diesel fuel, aviation fuel), often as a consequence of spills occurring during storage and/or active use. Various elements of the military are required to clean up contamination resulting from any activity on lands under their jurisdiction. Leakage occurring in underground storage tanks near ground water aquifers can be a particularly serious problem, resulting in contamination of ground water. The presence of petroleum hydrocarbon contaminants in flooded soils and sediments can pose unacceptable toxic hazards to the environment. A study was undertaken to examine the feasibility of using native soil micro-flora to degrade diesel fuels, fuel oil, and motor oils within the soil matrix; to isolate and identify those environmental factors controlling the rate and extent of degradation; and to develop procedures to optimize the rate and extent of biodegradation achieved.

  11. Calculation of vapor-liquid equilibrium and PVTx properties of geological fluid system with SAFT-LJ EOS including multi-polar contribution. Part III. Extension to water-light hydrocarbons systems

    NASA Astrophysics Data System (ADS)

    Sun, Rui; Lai, Shaocong; Dubessy, Jean

    2014-01-01

    The SAFT-LJ EOS improved by Sun and Dubessy (2010, 2012) is extended to water-light hydrocarbon systems. Light hydrocarbons (including CH4, C2H6, C3H8 and nC4H10) are modeled as chain molecules without multi-polar moments. The contributions of the shape of molecules and main intermolecular interactions existing in water-light hydrocarbon systems (including repulsive and attractive forces between Lennard-Jones segments, the hydrogen-bonding force and the multi-polar interaction between water molecules) to the residual Helmholtz energy were accounted for by this EOS. The adjustable parameters for the interactions of H2O-CH4, H2O-C2H6, H2O-C3H8, and H2O-nC4H10 pairs were evaluated from mutual solubility data of binary water-hydrocarbon systems at vapor-liquid equilibria. Comparison with the experimental data shows this SAFT-LJ EOS can represent well vapor-liquid (and liquid-liquid) equilibria of binary water-light hydrocarbon systems over a wide P-T range. The accuracy of this EOS for mutual solubilities of methane, ethane, propane and water is within the experimental uncertainty generally. Moreover, the model is able to accurately predict the vapor-liquid equilibria and PVTx properties of multi-component systems composed of water, light hydrocarbon as well as CO2. As we know, this EOS is the first one allowing quantitative calculation of the mutual solubilities of water and light hydrocarbons over a wide P-T range among SAFT-type EOSs. This work indicates that the molecular-based EOS combined with conventional mixing rule can well describe the thermodynamic behavior of highly non-ideal systems such as water-light hydrocarbons mixtures except in the critical region for which long range density fluctuations cannot be taken into account by this analytical model.

  12. Final report on CCM key comparison CCM.D-K2: Comparison of liquid density standards

    NASA Astrophysics Data System (ADS)

    Bettin, Horst; Jacques, Claude; Zelenka, Zoltán; Fujii, Ken-ichi; Kuramoto, Naoki; Chang, Kyung-Ho; Lee, Yong Jae; Becerra, Luis Omar; Domostroeva, Natalia

    2013-01-01

    The results are presented of the key comparison CCM.D-K2 that covered the density measurements of four liquids: the density of water at 20 °C, of pentadecane at 15 °C, 20 °C, 40 °C and 60°C, of tetrachloroethlyene at 5 °C and 20 °C and of a viscous oil at 20 °C. Seven national metrology institutes measured the densities at atmospheric pressure by hydrostatic weighing of solid density standards in the time interval from 27 April 2004 to 28 June 2004. Since the participants were asked not to include components for a possible drift or inhomogeneity of the liquid in their uncertainty budget, these uncertainty contributions are investigated for the final evaluation of the data. For this purpose, results of stability and homogeneity measurements of the pilot laboratory are used. The participants decided not to include a possible drift of the liquid's density since no significant drift could be detected, and the influence of the drift and its uncertainty are negligible. Similarly, the inhomogeneity of the water and pentadecane samples is not significant and has no influence on the evaluation. Thus, it was neglected. Only the inhomogeneities of tetrachloroethylene and of the viscous oil were significant. Consequently, they were included in the evaluation. With one or two exceptions, the results show good agreement among the participants. Only in the case of water are the results clearly discrepant. The key comparison reference values were calculated by the weighted mean (taking into account a small correlation between two participants) in the case of consistent results. Otherwise the Procedure B of Cox was used. The expanded uncertainties of all reference densities are below 1 × 10-5 in relative terms. This satisfies the needs of all customers who wish to calibrate or check liquid density measuring instruments such as oscillation-type density meters. The comparison fully supports the calibration measurement capabilities table in the BIPM key comparison database

  13. A validated liquid chromatographic method for the determination of polycyclic aromatic hydrocarbons in honey after homogeneous liquid-liquid extraction using hydrophilic acetonitrile and sodium chloride as mass separating agent.

    PubMed

    Koltsakidou, Anastasia; Zacharis, Constantinos K; Fytianos, Konstantinos

    2015-01-16

    In the present report, a simple and cost-effective method for the determination of twelve US EPA priority polycyclic aromatic hydrocarbons (PAHs) in honey samples after salting-assisted liquid-liquid extraction and UHPLC with fluorescence detection is proposed. The sample treatment is based on the usage of hydrophilic acetonitrile as extraction solvent and its phase separation under high salinity conditions. Due to the high sugar content of the samples the phase separation is promoted effortlessly. Several parameters affecting the extraction efficiency and method sensitivity including the concentration of the honey samples, the type and volume of the extraction solvent, the type and quantity of the inorganic salt, extraction time and centrifugation time was systematically investigated. The method was validated in-house according to the Commission Decision 2002/657/EC guidelines. The limit of detection (LOD) of the method lay between 0.02 and 0.04ngmL(-1) (corresponding to 0.08 and 0.16ngg(-1)) which are close to the quality criteria established by European Regulation (EC) 836/2011 concerning the PAHs in foodstuffs. The mean analytical bias (expressed as relative recoveries) in all spiking levels was acceptable being in the range of 54-118% while the relative standard deviation (RSD) was lower than 19%. The proposed method has been satisfactorily applied for the analysis of the selected PAHs residues in various honey samples obtained from Greek region.

  14. Simultaneous Determination of 13 Priority Polycyclic Aromatic Hydrocarbons in Tehran's Tap Water and Water for Injection Samples Using Dispersive Liquid-Liquid Micro Extraction Method and Gas Chromatography-Mass Spectrometry.

    PubMed

    Sadeghi, Ramezan; Kobarfard, Farzad; Yazdanpanah, Hassan; Eslamizad, Samira; Bayate, Mitra

    2016-01-01

    Polycyclic aromatic hydrocarbons (PAHs) are classified as persistent and carcinogenic organic pollutants. PAHs contamination has been reported in water. Many of relevant regulatory bodies such as EU and EPA have regulated the limit levels for PAHs in drinking water. In this study, 13 priority polycyclic aromatic hydrocarbons (PAHs) were determined in tap water samples of Tehran and water for injection. Dispersive liquid-liquid microextraction procedure combined with gas chromatography-mass spectrometry was used for the extraction and determination of PAHs in the samples. Under the optimized conditions, the range of extraction recoveries and relative standard deviations (RSDs) of PAHs in water using internal standard (anthracene-d10) were in the range of 71-90% and 4-16%, respectively. Limit of detection for different PAHs were between 0.03 and 0.1 ngmL(-1). The concentration of PAHs in all tap water as well as water for injection samples were lower than the limit of quantification of PAHs. This is the first study addressing the occurrence of PAHs in water for injection samples in Iran using dispersive liquid-liquid micro extraction procedure combined with gas chromatography-mass spectrometry.

  15. Simultaneous Determination of 13 Priority Polycyclic Aromatic Hydrocarbons in Tehran’s Tap Water and Water for Injection Samples Using Dispersive Liquid-Liquid Micro Extraction Method and Gas Chromatography-Mass Spectrometry

    PubMed Central

    Sadeghi, Ramezan; Kobarfard, Farzad; Yazdanpanah, Hassan; Eslamizad, Samira; Bayate, Mitra

    2016-01-01

    Polycyclic aromatic hydrocarbons (PAHs) are classified as persistent and carcinogenic organic pollutants. PAHs contamination has been reported in water. Many of relevant regulatory bodies such as EU and EPA have regulated the limit levels for PAHs in drinking water. In this study, 13 priority polycyclic aromatic hydrocarbons (PAHs) were determined in tap water samples of Tehran and water for injection. Dispersive liquid-liquid microextraction procedure combined with gas chromatography-mass spectrometry was used for the extraction and determination of PAHs in the samples. Under the optimized conditions, the range of extraction recoveries and relative standard deviations (RSDs) of PAHs in water using internal standard (anthracene-d10) were in the range of 71-90% and 4-16%, respectively. Limit of detection for different PAHs were between 0.03 and 0.1 ngmL-1. The concentration of PAHs in all tap water as well as water for injection samples were lower than the limit of quantification of PAHs. This is the first study addressing the occurrence of PAHs in water for injection samples in Iran using dispersive liquid-liquid micro extraction procedure combined with gas chromatography-mass spectrometry. PMID:27642318

  16. Reductive dechlorination of chlorinated hydrocarbons as non-aqueous phase liquid (NAPL): preliminary investigation on effects of cement doses.

    PubMed

    Do, Si-Hyun; Batchelor, Bill

    2012-07-15

    The reactivities of various types of iron mixtures to degrade chlorinated hydrocarbons (PCE, TCE and 1,1,1-TCA) in the form of non-aqueous phase liquids were investigated. The iron mixtures included a mixture of Fe(II) and Portland cement (Fe(II)-C), a mixture of Fe(II), Fe(III) and Ca(OH)(2) (Fe(II/III)-L), and a mixture of Fe(II), Fe(III), Ca(OH)(2), and Portland cement (Fe(II/III)-C). When the same amount of Fe(II) was used, Fe(II)-C was more reactive with chlorinated ethylenes (i.e. PCE and TCE) than Fe(II/III)-L. The reductive pathway for high concentrations of total PCE (i.e. above solubility) with Fe(II)-C was determined to be a combination of two-electron transfer, β-elimination and hydrogenolysis. Increasing the cement dose from 5% to 10% in Fe(II)-C did not affect PCE dechlorination rates, but it did favor the β-elimination pathway. In addition, when Fe(II/III)-C with 5%C was used, PCE dechlorination was similar to that by Fe(II)-C, but this mixture did not effectively degrade TCE. A modified second-order kinetic model was developed and shown to appropriately describe degradation of TCE at high concentrations. Fe(II/III)-L effectively degraded high concentrations of 1,1,1-TCA at rates that were similar to those obtained with Fe(II)-C using 10% C. Moreover, both increasing cement doses and the presence of Fe(III) increased dechlorination rates of 1,1,1-TCA, which was mainly through the hydrogenolysis pathway. The reactivity of Fe(II/III)-L was strongly dependent on the target compound (i.e. less reactivity with TCE, more with 1,1,1-TCA). Therefore, Fe(II/III)-L could be a potential mixture for degrading 1,1,1-TCA, but it should be modified to degrade TCE more effectively. Copyright © 2012 Elsevier B.V. All rights reserved.

  17. Combustion efficiency and altitude operational limits of three liquid hydrocarbon fuels having high volumetric energy content in a J33 single combustor

    NASA Technical Reports Server (NTRS)

    Stricker, Edward G

    1950-01-01

    Combustion efficiency and altitude operational limits were determined in a J33 single combustor for AN-F-58 fuel and three liquid hydrocarbon fuels having high volumetric energy content (decalin, tetralin, and monomethylnaphthalene) at simulated altitude and combustor inlet-air conditions. At the conditions investigated, the combustion efficiency for the four fuels generally decreased with an increase in volumetric energy content. The altitude operational limits for decalin and tetralin fuels were higher than for AN-F-58 fuel; monomethylnaphthalene fuel gave the lowest altitude operational limit.

  18. Final report on an experimental evaluation of remote sensing based hydrocarbon measurements: A comparison to fid measurements

    SciTech Connect

    Stephens, R.D.; Mulawa, P.A.; Giles, M.T.; Kennedy, K.G.; Groblicki, P.J.

    1994-09-01

    The purpose of the study was to intercompare hydrocarbon (HC) measurements performed by a number of different instruments: a gas chromatograph (GC), a flame ionizaton detector (FID), a fourier transform infrared spectrometer (FTIR), a commercially produced non-dispersive infrared analyzer (NDIR), and two remote sensors. These instruments were used to measure total HC concentrations in a variety of samples including (1) ten different individual HC species, (2) twelve different vehicle exhaust samples, and (3) three different volatilized fuel samples. The twelve exhaust samples were generated by operating two different vehicles on a dynamometer. Each vehicle was operated at different times with three different fuels.

  19. Production of reactive oxygen species by polyhalogenated cyclic hydrocarbons (PCH). Final report, 15 June 1990-14 June 1993

    SciTech Connect

    Stohs, S.J.

    1993-06-14

    During the past three years, excellent progress has been made relative to the specific objectives of this project. The results strongly support the hypothesis that the ability of polyhalogenated cyclic hydrocarbons (PCH) to induce production of reactive oxygen species may contribute to many of the toxic manifestations associated with these xenobiotics. As a consequence of the studies, seven papers have been presented at national and international meetings. In addition, twelve manuscripts have been published, three manuscripts are in press, and one manuscript has been submitted. Furthermore, several manuscripts are in the process of being written. Copies of the reprints and manuscripts are appended.

  20. Total hydrocarbon emission testing of waste-water sludge incinerators. Volume 1. Final report 1991-92

    SciTech Connect

    Chehaske, J.T.; DeWees, W.G.; Lewis, F.M.

    1992-06-01

    The U.S. EPA is considering continuous monitoring of total hydrocarbon (THC) emissions from all wastewater sludge incincerators. The study was conducted to determine the reliability of total hydrocarbon analyzers (THCAs) in the application. Continuous monitors for oxygen (O2), carbon monoxide (CO), THC, and temperature were installed at two municipal wastewater sludge incinerators. The O2 data were used to normalize the measured THC concentrations to 7% O2. CO was measured to determine if it could be used as a surrogate for THC measurements. The two THCAs performed very well, achieving 94 and 90% on-line availability at the two sampling sites, respectively. The O2 and CO analyzers also worked well. There were initial problems with the sample conditioning system that is necessary for the CO and O2 monitors, but successful operation was achieved after it was modified. The report presents graphical and tabular summaries of the results. The report covers a period from February 1991 to September 1991, and work was completed as of May 29, 1992.

  1. Analysis of the 16 Environmental Protection Agency priority polycyclic aromatic hydrocarbons by high performance liquid chromatography-oxidized diamond film electrodes.

    PubMed

    Bouvrette, Pierre; Hrapovic, Sabahudin; Male, Keith B; Luong, John H T

    2006-01-27

    The capabilities of using boron-doped diamond (BDD) thin films as electrode materials for analysis of the 16 US Environmental Protection Agency (EPA) priority polyaromatic hydrocarbons (PAHs) after a liquid chromatographic separation were evaluated. The BDD electrode was able to detect all 16 PAHs with high sensitivity due to the low background current and wide potential window. The method provided detection limits ranging from 12-40 nM (3-10 ppb) and repeatable results over consecutive analysis. Calibration curves were linear up to at least 10 microM for all PAHs. The work shows the promising use of diamond as an amperometric detector in high performance liquid chromatography (HPLC), especially for PAHs and other hydrophobic aromatic compounds.

  2. Synthesis of dimethyl ether and alternative fuels in the liquid phase from coal-derived synthesis gas. Final technical report

    SciTech Connect

    Not Available

    1993-02-01

    Through the mid-1980s, Air Products has brought the liquid phase approach to a number of other synthesis gas reactions where effective heat management is a key issue. In 1989, in response to DOE`s PRDA No. DE-RA22-88PC88805, Air Products proposed a research and development program entitled ``Synthesis of Dimethyl Ether and Alternative Fuels in the Liquid Phase from Coal Derived Syngas.`` The proposal aimed at extending the LPMEOH experience to convert coal-derived synthesis gas to other useful fuels and chemicals. The work proposed included development of a novel one-step synthesis of dimethyl ether (DME) from syngas, and exploration of other liquid phase synthesis of alternative fuel directly from syngas. The one-step DME process, conceived in 1986 at Air Products as a means of increasing syngas conversion to liquid products, envisioned the concept of converting product methanol in situ to DME in a single reactor. The slurry reactor based liquid phase technology is ideally suited for such an application, since the second reaction (methanol to DME) can be accomplished by adding a second catalyst with dehydration activity to the methanol producing reactor. An area of exploration for other alternative fuels directly from syngas was single-step slurry phase synthesis of hydrocarbons via methanol and DME as intermediates. Other possibilities included the direct synthesis of mixed alcohols and mixed ethers in a slurry reactor.

  3. Estimation of the Heat Balance of the Liquid Hydrocarbons Evaporation Process from the Open Surface During Geotechnical Monitoring

    NASA Astrophysics Data System (ADS)

    Zemenkova, M. Yu; Zemenkov, Yu D.

    2016-10-01

    Researchers in Tyumen State Oil and Gas University (TSOGU) have conducted a complex research of the heat and mass transfer processes and thermophysical properties of hydrocarbons, taking into account their impact on the reliability and safety of the hydrocarbon transport and storage processes. It has been shown that the thermodynamic conditions on the surface and the color of oil influence the degree of temperature rise in the upper layers of oil when exposed to direct solar radiation. In order to establish the nature of solar radiation impact on the surface temperature the experimental studies were conducted in TSOGU on the hydrocarbon evaporation and the temperature change of various petroleum and petroleum products on the free surface with varying degrees of thermal insulation of the side walls and bottom of the vessel.

  4. Determination of oxygen and nitrogen derivatives of polycyclic aromatic hydrocarbons in fractions of asphalt mixtures using liquid chromatography coupled to mass spectrometry with atmospheric pressure chemical ionization.

    PubMed

    Nascimento, Paulo Cicero; Gobo, Luciana Assis; Bohrer, Denise; Carvalho, Leandro Machado; Cravo, Margareth Coutinho; Leite, Leni Figueiredo Mathias

    2015-12-01

    Liquid chromatography coupled to mass spectrometry with atmospheric pressure chemical ionization was used for the determination of polycyclic aromatic hydrocarbon derivatives, the oxygenated polycyclic aromatic hydrocarbons and nitrated polycyclic aromatic hydrocarbons, formed in asphalt fractions. Two different methods have been developed for the determination of five oxygenated and seven nitrated polycyclic aromatic hydrocarbons that are characterized by having two or more condensed aromatic rings and present mutagenic and carcinogenic properties. The parameters of the atmospheric pressure chemical ionization interface were optimized to obtain the highest possible sensitivity for all compounds. The detection limits of the methods ranged from 0.1 to 57.3 μg/L for nitrated and from 0.1 to 6.6 μg/L for oxygenated derivatives. The limits of quantification were in the range of 4.6-191 μg/L for nitrated and 0.3-8.9 μg/L for oxygenated derivatives. The methods were validated against a diesel particulate extract standard reference material (National Institute of Standards and Technology SRM 1975), and the obtained concentrations (two nitrated derivatives) agreed with the certified values. The methods were applied in the analysis of asphalt samples after their fractionation into asphaltenes and maltenes, according to American Society for Testing and Material D4124, where the maltenic fraction was further separated into its basic, acidic, and neutral parts following the method of Green. Only two nitrated derivatives were found in the asphalt sample, quinoline and 2-nitrofluorene, with concentrations of 9.26 and 2146 mg/kg, respectively, whereas no oxygenated derivatives were detected. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  5. Extraction of S- and N-Compounds from the Mixture of Hydrocarbons by Ionic Liquids as Selective Solvents

    PubMed Central

    Gabrić, Beata; Sander, Aleksandra; Cvjetko Bubalo, Marina; Macut, Dejan

    2013-01-01

    Liquid-liquid extraction is an alternative method that can be used for desulfurization and denitrification of gasoline and diesel fuels. Recent approaches employ different ionic liquids as selective solvents, due to their general immiscibility with gasoline and diesel, negligible vapor pressure, and high selectivity to sulfur- and nitrogen-containing compounds. For that reason, five imidazolium-based ionic liquids and one pyridinium-based ionic liquid were selected for extraction of thiophene, dibenzothiophene, and pyridine from two model solutions. The influences of hydrodynamic conditions, mass ratio, and number of stages were investigated. Increasing the mass ratio of ionic liquid/model fuel and multistage extraction promotes the desulfurization and denitrification abilities of the examined ionic liquids. All selected ionic liquids can be reused and regenerated by means of vacuum evaporation. PMID:23843736

  6. Quasi-targeted analysis of hydroxylation-related metabolites of polycyclic aromatic hydrocarbons in human urine by liquid chromatography-mass spectrometry.

    PubMed

    Tang, Caiming; Tan, Jianhua; Fan, Ruifang; Zhao, Bo; Tang, Caixing; Ou, Weihui; Jin, Jiabin; Peng, Xianzhi

    2016-08-26

    Metabolite identification is crucial for revealing metabolic pathways and comprehensive potential toxicities of polycyclic aromatic hydrocarbons (PAHs) in human body. In this work, a quasi-targeted analysis strategy was proposed for metabolite identification of monohydroxylated polycyclic aromatic hydrocarbons (OH-PAHs) in human urine using liquid chromatography triple quadruple mass spectrometry (LC-QqQ-MS/MS) combined with liquid chromatography high resolution mass spectrometry (LC-HRMS). Potential metabolites of OH-PAHs were preliminarily screened out by LC-QqQ-MS/MS in association with filtering in a self-constructed information list of possible metabolites, followed by further identification and confirmation with LC-HRMS. The developed method can provide more reliable and systematic results compared with traditional untargeted analysis using LC-HRMS. In addition, data processing for LC-HRMS analysis were greatly simplified. This quasi-targeted analysis method was successfully applied to identifying phase I and phase II metabolites of OH-PAHs in human urine. Five metabolites of hydroxynaphthalene, seven of hydroxyfluorene, four of hydroxyphenanthrene, and three of hydroxypyrene were tentatively identified. Metabolic pathways of PAHs in human body were putatively revealed based on the identified metabolites. The experimental results will be valuable for investigating the metabolic processes of PAHs in human body, and the quasi-targeted analysis strategy can be expanded to the metabolite identification and profiling of other compounds in vivo.

  7. Sorption and transport of polynuclear aromatic hydrocarbons in low-carbon aquifer materials. Final report, Jan 88-Jan 89

    SciTech Connect

    Lion, L.W.

    1990-12-01

    Sorption studies of polycyclic aromatic hydrocarbons (PAH) on low-carbon aquifer materials are reported. Both column and batch partition coefficients (Kd) were affected by synthetic polymeric components, such as Teflon, in commonly used experimental apparatus. These influences include incorrect estimates for Kd and tailing of peaks in column studies. Both batch and column experimental methods are developed, using polymer-free systems, that allow accurate measurement of Kds for hydrophobic PAHs in low carbon systems. Application of these methods shows that organic carbon contents below the commonly cited threshold level of 0.1 percent may dominate the partitioning and subsequent transport of phenanthrene in aquifer systems. Calculated Kd values from batch and column (temporal first moment) techniques did not agree. Reasons for the disparity in the results from these methods are discussed. Column results may be described using the batch Kd and two adjustable fitting parameters representing variables in a two-side kinetic model.

  8. Final optics protection in laser inertial fusion with cryogenic liquid droplets

    SciTech Connect

    Moir, R W

    2000-08-31

    A burst of x rays and vaporized debris from high yield targets can damage the final optics in laser inertial fusion energy (IFE) power plants and in laboratory experimental facilities such as the National Ignition Facility (NIF) or Laser MegaJoule (LMJ). Noble gases such as Xe or Kr have been proposed to protect final optics from target-produced x rays and debris. Some problems with the use of such ambient gas fills are the large amount of gas involved, heat transfer to a cryogenic target, potential resonant reradiation of x rays absorbed, and a nonuniform index of refraction due to turbulence interfering with the focusing of laser light. Also the fast igniter laser intensity may be too great for propagation through an ambient gas. We propose to provide the gas in the form of many small closely spaced liquid droplets injected in front of the optics. In the case of NIF, the droplets would be injected only when needed just before a high yield shot. The laser light that is absorbed will cause evaporation of the liquid and spreading of this gas. The liquid droplets intercept only {approx}5% of the laser light allowing {approx}95% to pass through to the target. The light absorbed in the NIF example (assumed to be 50% of the intercepted light, whose intensity is 3.6 x 10{sup 9} W/cm{sup 2}) would cause the xenon droplets to evaporate and spread uniformly such that the x rays from 10 eV to 2 keV are appreciably attenuated when they arrive 40 to 70 ns later at the optical surface. X rays above 3 keV and below 10 eV are not attenuated very much but their intensities are rapidly falling off in this range anyway. Typical droplet sizes are {approx}10 {micro}m radius with a spacing of {approx}0.4 mm. The gas would also protect vaporized target debris from condensing on the optics due to the 0.2 mg/cm{sup 2} of xenon (5 x 10{sup 17} cm{sup -2} or 8 Torr-cm for l-e-folding of 1 keV x-rays). These droplets might be produced with technology similar to ink jet technology and photo

  9. Survey of cotton (Gossypium sp.) for non-polar, extractable hydrocarbons for use as petrochemicals and liquid fuels

    USDA-ARS?s Scientific Manuscript database

    An ontogenetic study of a commercial cotton cultivar (FiberMax 1320), grown dryland, revealed that the dry weight (DW) of leaves reached a maximum at the 1st flower stage, and then declined as bolls opened. However, % pentane soluble hydrocarbon (HC) yield continued to increase throughout the growi...

  10. Comparative evaluation of coal conversion technologies. Final report, December 7, 1982-July 6, 1983. [Davy McKee (COCHAR), Exxon (Exxon Donor Solvent), Lurgi process, Occidental Research Corporation (Flash Pyrolysis), Tosco (TOSCOAL), Union Carbide (Hydrocarbonization)

    SciTech Connect

    Robinson, C.W.

    1983-09-01

    A comparative evaluation was made of six coal pyrolysis processes developed by the following companies: Davy McKee (COCHAR), Exxon (Exxon Donor Solvent), Lurgi (Lurgi Ruhrgas), Occidental Research Corporation (Flash Pyrolysis), Tosco (TOSCOAL), Union Carbide (Hydrocarbonization). This study serves as the necessary first step to the development of a major coal pyrolysis plant based on San Juan Basin coal. The process evaluation led to the recommendation that a more detailed study be made of the integration of the Union Carbide Hydrocarbonization process with an existing coal-fired electric utility plant in the Four Corners. The study included investigations of a char/coal liquids slurry movement to Texas or California, of the hydrotreating of coal liquids produced by the Hydrocarbonization process, and of the cleaning of San Juan Basin coal by electrostatic separation. Estimates of the capital and operating costs of a Hydrocarbonization plant located adjacent to the Four Corners Power Plant were prepared. A forecast was made of the economic benefits to the state of New Mexico and the number of jobs which would be created by the construction of a hydrocarbonization plant. A work plan was created to guide the project through the next stage of development. 58 references, 1 figure, 5 tables.

  11. The Mochovce final treatment center for liquid radioactive waste introduced to active trial operation

    SciTech Connect

    Krajc, T.; Stubna, M.; Kravarik, K.; Zatkulak, M.; Slezak, M.; Remias, V.

    2007-07-01

    The Final Treatment Centre (FTC) for Mochovce Nuclear Power Plant (NPP) have been designed for treatment and final conditioning of radioactive liquid and wet waste produced by named NPP equipped with Russian VVER-440 type of reactors. Treated wastes comprise radioactive concentrates, spent resin and sludge. VUJE Inc. as an experienced company in field of treatment of radioactive waste in Slovakia has been chosen as main contractor for technological part of FTC. During the realisation of project the future operator of Centre required the contractor to solve the treatment of wastes produced in the process of NPP A-1 decommissioning. On the basis of this requirement the project was modified in order to enable manipulations with waste products from A-1 NPP transported to Centre in steel drums. The initial project was prepared in 2003. The design and manufacture of main components were performed in 2004 and 2005. FTC civil works started in August 2004. Initial nonradioactive testing of the system parts were carried out from April to September 2006, then the tests of systems started with model concentrates and non-radioactive resins. After the processes evaluation the radioactive test performed from February 2007. A one-year trial operation of facility is planned for completion during 2007 and 2008. The company JAVYS, Inc. is responsible for radioactive waste and spent fuel treatment in the Slovak republic and will operate the FTC during trial operation and after its completion. This Company has also significant experience with operation of Jaslovske Bohunice Treatment Centre. The overall capacity of the FTC is 820 m{sup 3}/year of concentrates and 40 m{sup 3}/year of spent resin and sludge. Bituminization and cementation were provided as main technologies for treatment of these wastes. Treatment of concentrate is performed by bituminization on Thin Film Evaporator with rotating wiping blades. Spent resin and sludge are decanted, dried and mixed with bitumen in blade

  12. Final Treatment Center Project for Liquid and Wet Radioactive Waste in Slovakia

    SciTech Connect

    Kravarik, K.; Stubna, M.; Pekar, A.; Krajc, T.; Zatkulak, M.; Holicka, Z.; Slezak, M.

    2006-07-01

    The Final Treatment Center (FTC) for Mochovce nuclear power plant (NPP) is designed for treatment and final conditioning of radioactive liquid and wet waste produced from plant operation. Mochovce NNP uses a Russian VVER-440 type reactor. Treated wastes comprise radioactive concentrates, spent resin and sludge. VUJE Inc. as an experienced company in field of treatment of radioactive waste in Slovakia has been chosen as main contractor for technological part of FTC. This paper describes the capacity, flow chart, overall waste flow and parameters of the main components in the FTC. The initial project was submitted for approval to the Slovak Electric plc. in 2003. The design and manufacture of main components were performed in 2004 and 2005. FTC construction work started early in 2004. Initial non-radioactive testing of the system is planned for summer 2006 and then radioactive tests are to be followed. A one-year trial operation of facility is planned for completion in 2007. SE - VYZ will be operates the FTC during trial operation and after its completion. SE - VYZ is subsidiary company of Slovak Electric plc. and it is responsible for treatment with radioactive waste and spent fuel in the Slovak republic. SE - VYZ has, besides of other significant experience with operation of Jaslovske Bohunice Treatment Centre. The overall capacity of the FTC is 870 m{sup 3}/year of concentrates and 40 m{sup 3}/year of spent resin and sludge. Bituminization and cementation were provided as main technologies for treatment of these wastes. Treatment of concentrate is performed by bituminization. Concentrate and bitumen are metered into a thin film evaporator with rotating wiping blades. Surplus water is evaporated and concentrate salts are embedded in bitumen. Bitumen product is discharged into 200 l steel drums. Spent resin and sludge are decanted, dried and mixed with bitumen. These mixtures are also discharged into 200 l steel drums. Drums are moved along bituminization line on a

  13. Experimental investigation of the effects of aromatic hydrocarbons on a sediment food web. University research initiative. Final draft report

    SciTech Connect

    Carman, K.R.; Fleeger, J.W.; Pomarico, S.M.; Conn, C.; Todaro, A.

    1994-07-01

    The influence of polynuclear aromatic hydrocarbons (PAH) on a sedimentary salt-marsh food web was examined using microcosm and laboratory experiments that simulated natural conditions. Microcosms were dosed with concentrations of PAH-contaminated sediment collected from a produced water site at Pass Fourchon, LA. Bacterial activity and abundance were not influenced by PAH, but microalgal activity and physiological condition were. Grazing by copepods on benthic microalgae was not significantly influenced by PAH concentration, nor was the physiological condition of copepods. Meiofaunal community composition was influenced by PAH, as nematodes became disproportionally abundant, and the nauplius/copepod ratio increased in high-PAH treatments. Overall, sublethal effects of PAH were not pronounced at the concentrations (0.3 to 3.0 ppm) we examined. Fish-predation studies indicated that Leiostomus xanthurus could not detect PAH-contaminated sediments, and continued to feed normally when exposed to them. PAH contamination did not decrease the number of feeding strikes or sediment processing time. This lack of ability to discriminate between contaminated and uncontaminated sediments could have serious implications in terms of bioaccumulation of PAH (or other contaminants) by these bottom-feeding fish.

  14. Diagnostic development for determining the joint temperature/soot statistics in hydrocarbon-fueled pool fires : LDRD final report.

    SciTech Connect

    Casteneda, Jaime N.; Frederickson, Kraig; Grasser, Thomas W.; Hewson, John C.; Kearney, Sean Patrick; Luketa, Anay Josephine

    2009-09-01

    A joint temperature/soot laser-based optical diagnostic was developed for the determination of the joint temperature/soot probability density function (PDF) for hydrocarbon-fueled meter-scale turbulent pool fires. This Laboratory Directed Research and Development (LDRD) effort was in support of the Advanced Simulation and Computing (ASC) program which seeks to produce computational models for the simulation of fire environments for risk assessment and analysis. The development of this laser-based optical diagnostic is motivated by the need for highly-resolved spatio-temporal information for which traditional diagnostic probes, such as thermocouples, are ill-suited. The in-flame gas temperature is determined from the shape of the nitrogen Coherent Anti-Stokes Raman Scattering (CARS) signature and the soot volume fraction is extracted from the intensity of the Laser-Induced Incandescence (LII) image of the CARS probed region. The current state of the diagnostic will be discussed including the uncertainty and physical limits of the measurements as well as the future applications of this probe.

  15. Ultrahigh-current-density metal-ion implantation and diamondlike-hydrocarbon films for tribological applications; Final report

    SciTech Connect

    Wilbur, P.J.

    1993-09-01

    The metal-ion-implantation system used to implant metals into substrates are described. The metal vapor required for operation is supplied by drawing sufficient electron current from the plasma discharge to an anode-potential crucible so a solid, pure metal placed in the crucible will be heated to the point of vaporization. The ion-producing, plasma discharge is initiated within a graphite-ion-source body, which operates at high temperature, by using an argon flow that is turned off once the metal vapor is present. Extraction of ion beams several cm in diameter at current densities ranging to several hundred {mu}A/cm{sup 2} on a target 50 cm downstream of the ion source have been demonstrated using Mg, Ag, Cr, Cu, Si, Ti, V, B and Zr. These metals were implanted into over 100 substrates (discs, pins, flats, wires). A model describing thermal stresses induced in materials (e.g. ceramic plates) during high-current-density implantation is presented. Tribological and microstructural characteristics of iron and 304-stainless-steel samples implanted with Ti or B are examined. Diamondlike-hydrocarbon coatings were applied to steel surfaces and found to exhibit good tribological performance.

  16. Evaluation of polyurethane foam cartridges for measurement of polynuclear aromatic hydrocarbons in air. Final report, 1 August-31 December 1984

    SciTech Connect

    Chuang, C.C.; Bresler, W.E.; Hannan, S.W.

    1985-08-01

    The objective of this project was to evaluate polyurethane foam (PUF) cartridges as collection media for quantification of vapor-phase polynuclear aromatic hydrocarbons (PAHs) in air. Two cleanup methods for PUF cartridges--compression rinsing and combined compression rinsing and Soxhlet extraction--were evaluated. Both methods successfully remove interfering material and background PAHs from the PUF. The compression rinsing method is recommended because it is easier, faster, and cheaper. Two procedures for extraction of PAHs from the PUF matrix, Soxhlet extraction and compression rinsing, were compared. These sample extracts were analyzed by on-column injection, electron impact gas chromatography/mass spectrometry (EI GC/MS) to determine PAHs. The results showed that compression rinsing is comparable to conventional Soxhlet extraction, and that both methods successfully remove PAHs from the PUF cartridges. The compression rinsing method was then used in the stability study. The stability study was carried out to determine the stability of PAHs adsorbed on PUF cartridges as a function of storage time between collection and extraction. The results indicated that the levels of the spiked perdeuterated benzo(a)pyrene decreased significantly during storage. The rate of decrease was much faster when the PUF cartridges were stored in light. Other PAH levels were not adversely influenced by the storage time.

  17. Plant hydrocarbon recovery process

    SciTech Connect

    Dzadzic, P.M.; Price, M.C.; Shih, C.J.; Weil, T.A.

    1982-01-26

    A process for production and recovery of hydrocarbons from hydrocarbon-containing whole plants in a form suitable for use as chemical feedstocks or as hydrocarbon energy sources which process comprises: (A) pulverizing by grinding or chopping hydrocarbon-containing whole plants selected from the group consisting of euphorbiaceae, apocynaceae, asclepiadaceae, compositae, cactaceae and pinaceae families to a suitable particle size, (B) drying and preheating said particles in a reducing atmosphere under positive pressure (C) passing said particles through a thermal conversion zone containing a reducing atmosphere and with a residence time of 1 second to about 30 minutes at a temperature within the range of from about 200* C. To about 1000* C., (D) separately recovering the condensable vapors as liquids and the noncondensable gases in a condition suitable for use as chemical feedstocks or as hydrocarbon fuels.

  18. Utilization of stable carbon isotope in the verification of bioremediation of chlorinated hydrocarbons. Final report, July--December 1995

    SciTech Connect

    DeFlaun, M.F.; Steffan, R.J.; Van de Velde, K.

    1996-10-01

    The overall goal of this work was to test the feasibility of using stable carbon isotope analysis to verify in situ biodegradation of hydrocarbons and chlorinated ethenes under aerobic conditions. Specific objectives were to (1) determine d{sup 13}C values for TCE and the various compounds to be used as co- substrates for TCE degradation; (2) evaluate effects of aerobic biodegradation of co-substrate compounds and TCE on gross fractionation of carbon isotopes as measured in the resulting CO{sub 2}; (3) test the carbon isotope method for its ability to differentiate the source of the CO{sub 2} resulting from aerobic biodegradation; and (4) use samples from an appropriately contaminated bioventing site. Different degrees of fractionation were measured in both pure and mixed cultures for the different compounds tested in this study. Fractionation for toluene was slightly more negative than the starting compound. For JP-4, the fractionation of JP-4 resulted in d{sup 13}C values much more negative than the starting compound. Fractionation for TCE results in d{sup 13}C values more positive, indicating the CO{sub 2} had a higher percentage of {sup 13}C than the source compound. A mixture of toluene and TCE had a d{sup 13}C value intermediate between the two. These results indicate, with the d{sup 13}C values for these co-substrates and chlorinated ethenes sufficiently different, the degradation of one or the other can be determined. When both are being degraded an intermediate value can be obtained.

  19. Interim response action basin F liquid incineration project final draft human health risk assessment. Volume 1. Final draft report

    SciTech Connect

    1991-07-01

    This document is a comprehensive, multiple exposure pathway, human health risk assessment prepared for the proposed Basin F Liquid Incineration Project. The submerged quench incinerator will treat Basin F liquid and hydrazine rinse water. The objective of the risk assessment is to establish chemical emission limits which are protective of human health. Average and maximum lifetime daily intakes were calculated for adults, children, and infants in four maximum exposure scenarios under base case and sensitivity case emissions condition. It was concluded that the incineration facility poses neither carcinogenic nor noncarcinogenic risk to any sensitive population. The assessment is divided into: (1) Incineration facility description; (2) Description of surrounding area; (3) Process of pollutant identification and selection; and (4) Determination of emission rates from incineration facility.

  20. 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.

  1. Stir bar sorptive extraction and high-performance liquid chromatography-fluorescence detection for the determination of polycyclic aromatic hydrocarbons in Mate teas.

    PubMed

    Zuin, Vânia Gomes; Montero, Larisse; Bauer, Coretta; Popp, Peter

    2005-10-14

    A simple procedure based on stir bar sorptive extraction (SBSE) and high-performance liquid chromatography-fluorescence detection (HPLC-FLD) is presented for the determination of 15 polycyclic aromatic hydrocarbons (PAHs) in herbal tea prepared with Mate leaves (Ilex paraguariensis St. Hil.). The influence of methanol and salt addition to the samples, the extraction time, the desorption time and the number of desorption steps, as well as the matrix effect, were investigated. Once the SBSE method was optimised (10 mL of Mate tea, 2h extraction at room temperature followed by 15 min desorption in 160 microL of an acetonitrile (ACN)-water mixture), analytical parameters such as repeatability (< or = 10.1%), linearity (r2 > or = 0.996), limit of detection (LOD, 0.1-8.9 ng L(-1) ), limit of quantitation (LOQ, 0.3-29.7 ng L(-1) and absolute recovery (24.2-87.0%) were determined. For calibration purposes, a reference sample was firstly obtained by removing the analytes originally present in the lowest contaminated Mate tea studied (via SBSE procedure) and then spiked at 1-1200 ng L(-1)range. The proposed methodology proved to be very convenient and effective, and was successfully applied to the analysis of 11 Mate tea samples commercialised in Brazil. The results of the commercial Mate tea samples found by the SBSE approach were compared with those obtained by liquid-liquid extraction (LLE), showing good agreement.

  2. Optimization of pressurized liquid extraction (PLE) for rapid determination of mineral oil saturated (MOSH) and aromatic hydrocarbons (MOAH) in cardboard and paper intended for food contact.

    PubMed

    Moret, Sabrina; Sander, Maren; Purcaro, Giorgia; Scolaro, Marianna; Barp, Laura; Conte, Lanfranco S

    2013-10-15

    Packaging can represent a primary source of food contamination with mineral oil saturated hydrocarbons (MOSH) and aromatic hydrocarbons (MOAH), especially when recycled cardboard or mineral oil based printing inks are used. A pressurized liquid extraction (PLE) method, followed by on-line LC-GC analysis, has been optimized for rapid mineral oil determination in cardboard and paper samples. The proposed method involves extraction with hexane (2 cycles) at 60°C for 5 min, and allows for the processing of up to 6 samples in parallel with minimal sample manipulation and solvent consumption. It gave good repeatability (coefficient of variation lower than 5%) and practically quantitative extraction yield (less than 2% of the total contamination found in a third separate cycle). The method was applied to different cardboards and paper materials intended for food contact. Results obtained were similar to those obtained by applying classical solvent extraction with hexane/ethanol 1:1 (v/v) as described by Lorenzini et al. [20].

  3. Determination of polycyclic aromatic hydrocarbons in fractions in asphalt mixtures using liquid chromatography coupled to mass spectrometry with atmospheric pressure chemical ionization.

    PubMed

    Nascimento, Paulo Cicero; Gobo, Luciana Assis; Bohrer, Denise; Carvalho, Leandro Machado; Cravo, Margareth Coutinho; Leite, Leni Figueiredo Mathias

    2015-07-01

    An analytical method using liquid chromatography coupled to mass spectrometry with atmospheric pressure chemical ionization for the determination of polycyclic aromatic hydrocarbons in asphalt fractions has been developed. The 14 compounds determined, characterized by having two or more condensed aromatic rings, are expected to be present in asphalt and are considered carcinogenic and mutagenic. The parameters of the atmospheric pressure chemical ionization interface were optimized to obtain the highest possible sensitivity for all of the compounds. The limits of detection ranged from 0.5 to 346.5 μg/L and the limits of quantification ranged from 1.7 to 1550 μg/L. The method was validated against a diesel particulate extract standard reference material (NIST SRM 1975), and the obtained concentrations agreed with the certified values. The method was applied to asphalt samples after its fractionation according to ASTM D4124 and the method of Green. The concentrations of the seven polycyclic aromatic hydrocarbons quantified in the sample ranged from 0.86 mg/kg for benzo[ghi]perylene to 98.32 mg/kg for fluorene. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  4. Rapid determination of trace polycyclic aromatic hydrocarbons in particulate matter using accelerated solvent extraction followed by ultra high performance liquid chromatography with fluorescence detection.

    PubMed

    Xu, Tianci

    2016-05-01

    A method has been developed for the trace analysis of polycyclic aromatic hydrocarbons, which are known as persistent organic pollutants and ubiquitous constituents of fine particulate matter that causes growing airborne pollution. The method, which was especially for samples of airborne particulate matter less than 2.5 μm in diameter, utilized accelerated solvent extraction and ultra high performance liquid chromatography with fluorescence detector. Four principal parameters of accelerated solvent extraction were optimized to obtain maximum extraction efficiency. Using the established synergetic programs of gradient elution and fluorescence wavelength switching, a rapid separation was achieved in 6.56 min with good linearity for 15 polycyclic aromatic hydrocarbons (coefficient of determination above 0.999). The limits of detection ranged from 0.833 to 10.0 pg/m(3) . The precision of the method expressed as inter-day relative standard deviation ranged from 0.2 to 1%, which was calculated from nine repetitive measurements of 8.00 μg/L analytes. Average spiked recoveries ranged from 71.6 to 97.7%, with the exception of naphthalene. The rapid, sensitive, and accurate method can meet the pressing needs of health risk assessment and increasingly heavy daily tasks of air quality monitoring. © 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  5. New Insight into the Formation Mechanism of Imidazolium-Based Ionic Liquids from N-Alkyl Imidazoles and Halogenated Hydrocarbons: A Polar Microenvironment Induced and Autopromoted Process.

    PubMed

    Mu, Xueli; Jiang, Nan; Liu, Chengbu; Zhang, Dongju

    2017-02-09

    To illustrate the formation mechanism of imidazolium-based ionic liquids (ILs) from N-alkyl imidazoles and halogenated hydrocarbons, density functional theory calculations have been carried out on a representative system, the reaction of N-methyl imidazole with chloroethane to form 1-ethyl-3-methyl imidazolium chloride ([Emim]Cl) IL. The reaction is shown to proceed via an SN2 transition state with a free energy barrier of 34.4 kcal/mol in the gas phase and 27.6 kcal/mol in toluene solvent. The reaction can be remarkably promoted by the presence of ionic products and water molecules. The calculated barriers in toluene are 22.0, 21.7, and 19.9 kcal/mol in the presence of 1-3 ionic pairs of [Emim]Cl and 23.5, 21.3, and 19.4 kcal/mol in the presence of 1-3 water molecules, respectively. These ionic pairs and water molecules do not participate directly in the reaction but provide a polar environment that favors stabilizing the transition state with large charge separation. Hence, we propose that the synthesis of imidazolium-based ILs from N-alkyl imidazoles and halogenated hydrocarbons is an autopromoted process and a polar microenvironment induced reaction, and the existence of water molecules (a highly polar solvent) in the reaction may be mainly responsible for the initiation of reaction.

  6. 75 FR 19991 - Notice of Availability of the Final Environmental Impact Statement for the UNEV Refined Liquid...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-04-16

    ... Refined Liquid Petroleum Products Pipeline in Utah and Nevada and the Proposed Amendment of the Pony... Petroleum Products Pipeline and Pony Express Proposed RMPA/Final EIS have been sent to affected Federal... Pony Express Resource Management Plan so that it would be consistent with the grant of a...

  7. Comparison of low-level polycyclic aromatic hydrocarbons in sediment revealed by Soxhlet extraction, microwave-assisted extraction, and pressurized liquid extraction.

    PubMed

    Itoh, Nobuyasu; Numata, Masahiko; Aoyagi, Yoshie; Yarita, Takashi

    2008-03-31

    We analyzed polycyclic aromatic hydrocarbons (PAHs) present in lake sediment at low levels (<1 microg g(-1)) by using Soxhlet extraction (Soxhlet), microwave-assisted extraction (MAE), and pressurized liquid extraction (PLE) in combination with gas chromatography and isotope-dilution mass spectrometry. Although all extraction techniques showed good repeatability for five target PAHs (relative standard deviation <5.2%, n=3), the results decreased in the order PLE>MAE>Soxhlet. Differences in the results originated mainly from differences in the extraction efficiencies of the techniques for native PAHs, because all techniques gave comparable recovery yields of corresponding 13C-labeled PAHs (13C-PAHs) (51-84%). Since non-negligible amounts of both native PAHs and 13C-PAHs were re-adsorbed on matrix in MAE, not only recovery yields of 13C-PAHs but also efficiencies of extraction of native PAHs should be examined to evaluate the appropriateness of any analytical procedures.

  8. Storing solar energy with liquid phase Diels-Alder reactions. Final report

    SciTech Connect

    Poling, B.E.

    1983-07-28

    At the beginning of this project, a preliminary study was completed that indicated the Diels-Alder reaction between maleic anhydride and 2 methyl furan had an energy storage capacity greater than water. During the last two years when this grant was in effect, three additional projects have been completed. First, an improved calorimetric techniques was developed for determination of the energy storage capacity of a reversible liquid phase chemical reaction. This technique confirmed the validity of the earlier results for the maleic anhydride-methyl furan reaction. Second, a technique was developed for characterizing solution nonidealities for mixtures in which reversible chemical reactions occur. It was found that for the maleic anhydride-2 methyl furan reaction, these non idealities could affect equilibrium compositions by nearly 40%. Third, drop calorimetry was used as a screening method to examine sixteen reactions for their potential as energy storage candidates. Of the sixteen examined, three (all involving maleic anhydride and substituted furan) showed an increased energy storage capacity due to reaction while the remaining thirteen showed no increase. In the following report, results of these three studies are summarized. Finally, a general summary of the status of energy storage by chemical reactions is presented.

  9. Thermodynamic and rheological properties of solid-liquid systems in coal processing. Final technical report

    SciTech Connect

    Kabadi, V.N.

    1995-06-30

    The work on this project was initiated on September 1, 1991. The project consisted of two different tasks: (1) Development of a model to compute viscosities of coal derived liquids, and (2) Investigate new models for estimation of thermodynamic properties of solid and liquid compounds of the type that exist in coal, or are encountered during coal processing. As for task 1, a model for viscosity computation of coal model compound liquids and coal derived liquids has been developed. The detailed model is presented in this report. Two papers, the first describing the pure liquid model and the second one discussing the application to coal derived liquids, are expected to be published in Energy & Fuels shortly. Marginal progress is reported on task 2. Literature review for this work included compilation of a number of data sets, critical investigation of data measurement techniques available in the literature, investigation of models for liquid and solid phase thermodynamic computations. During the preliminary stages it was discovered that for development of a liquid or solid state equation of state, accurate predictive models for a number of saturation properties, such as, liquid and solid vapor pressures, saturated liquid and solid volumes, heat capacities of liquids and solids at saturation, etc. Most the remaining time on this task was spent in developing predictive correlations for vapor pressures and saturated liquid volumes of organic liquids in general and coal model liquids in particular. All these developments are discussed in this report. Some recommendations for future direction of research in this area are also listed.

  10. Biomass Conversion to Produce Hydrocarbon Liquid Fuel Via Hot-vapor Filtered Fast Pyrolysis and Catalytic Hydrotreating

    SciTech Connect

    Wang, Huamin; Elliott, Douglas C.; French, Richard J.; Deutch, Steve; Iisa, Kristiina

    2016-01-01

    Experimental methods for fast pyrolysis of lignocellulosic biomass to produce bio-oils and for the catalytic hydrotreating of bio-oils to produce fuel range hydrocarbons are presented. Hot-vapor filtration during fast pyrolysis to remove fine char particles and inorganic contaminants from bio-oil was also assessed. This is the first draft of our video publication for Jove. The manuscript is approved previously as PNNL-SA-108525. Please access the video via http://www.jove.com/video/54088?status=a56094k.

  11. Use of neural networks for prediction of vapor/liquid equilibrium K values for light-hydrocarbon mixtures

    SciTech Connect

    Habiballah, W.A.; Startzman, R.A.; Barrufet, M.A.

    1996-05-01

    Equilibrium ratios play a fundamental role in the understanding of phase behavior of hydrocarbon mixtures. They are important in predicting compositional changes under varying temperature and pressure in reservoirs, surface separators, and production and transportation facilities. In particular, they are critical for reliable and successful compositional reservoir simulation. This paper presents a new approach for predicting K values with neural networks (NN`s). The method is applied to binary and multicomponent mixtures, and K-value prediction accuracy is on the order of the traditional methods. However, computing speed is significantly faster.

  12. Final Report: Developing Liquid Protection Schemes for Fusion Energy Reactor First Walls

    SciTech Connect

    Minami Yoda Said I. Abdel-Khalik

    2006-03-29

    Over the last year, the Georgia Tech group has experimentally studied vertical turbulent sheets of water issuing downwards into atmospheric pressure air at Reynolds numbers Re = U{sub 0}{delta}/{nu} = 53,000 and 120,000 and Weber numbers We = {rho}U{sub o} {sup 2}{delta}/{sigma} = 2,900 and 18,000, respectively. Here, U{sub o} is the average jet speed, {delta} is the jet thickness (short dimension) at the nozzle exit ({delta} = 1 cm), and {nu}, {rho} and {sigma} are the kinematic viscosity and density of water and the surface tension at the air-water interface, respectively. These Re and We values are about 50% and 20% of the prototypical values for HYLIFE-II, respectively. In this report, the flow coordinate system is defined so that the origin is at the center of the nozzle exit, with the x-axis along the flow direction, the y-axis along the long dimension of the nozzle, and the z-axis along the short dimension of the nozzle (cf. Fig. 1). During the final year of this project, we have made three contributions in the area of thermal-hydraulics of thick liquid protection, namely: (1) Experimentally demonstrated that removing as little as 1% of the total mass flux using boundary-layer (BL) cutting can reduce the number density of the drops due to turbulent breakup of the liquid sheet below the maximum background density levels recommended for HYLIFE-II of 5 x 10{sup -19} m{sup 3}; (2) Shown that a well-designed flow conditioning section upstream of the nozzle can greatly reduce surface ripple, and that boundary-layer cutting can be used in conjunction with well-designed flow conditioning to further reduce surface ripple below the 0.07{delta} beam-to-jet standoff proposed for HYLIFE-II; and (3) Quantified how different flow conditioner designs affect the rms fluctuations of the streamwise (x) and transverse (z) velocity components in the nozzle itself (i.e., upstream of the nozzle exit) and affect surface ripple in the near-field of the flow, or x {le} 25{delta}. The

  13. Biodesulfurization of mild gasification liquid products. Final technical report, 1 September, 1992--31 August, 1993

    SciTech Connect

    Kilbane, J.J. II

    1993-12-31

    The mild gasification of coal, as being developed at IGT and elsewhere, is a promising new technology that can convert coal to multiple products: gas, solid, and liquids. Mild gasification liquids can be used as feedstock to make transportation fuels and chemicals. However, the sulfur content and aromaticity of mild gasification liquids limits their usefulness and biodesulfurization can potentially decrease both sulfur content and aromaticity. The objective of this project is to investigate and feasibility of using biodesulfurization to upgrade the quality of mild gasification liquids. During this project, it was shown that the middle distillate (360--440 F) fraction of liquids derived from the mild gasification of coal, and unfractionated liquids can be biodesulfurized. Moreover, it was demonstrated that lysed cell preparations and freeze-dried cells can be used to biodesulfurize mild coal gasification liquids. The importance of the finding that freeze-dried biocatalysts can be used to biodesulfurize mild coal gasification liquids is that freeze-dried cells can be produced at one location, stored indefinitely, and then shipped (at reduced weight, volume, and cost) to another location for coal biodesulfurization. Moreover, freeze-dried biocatalysts can be added directly to mild coal gasification liquids with only minimal additions of water so that reactor volumes can be minimized.

  14. Liquid chromatographic analysis of coal surface properties. Final report, September 1991--February 1995

    SciTech Connect

    Kwon, K.C.

    1996-03-01

    Experiments on equilibrium adsorption loadings of various probe compounds on 60-200 mesh Illinois {number_sign}6 coal (PSOC-1539), Adaville {number_sign}1 coal (PSOC-1544), Wyodak coal (PSOC-1545) and Pittsburgh {number_sign}8 coal (PSOC-1549) were performed. the probe compounds include m-cresol, p-cresol, o-cresol, phenol, n-octanol, n-heptanol, n-propanol, isopropanol n-butanol, s-butanol, 2-butanol, t-butanol, 2-naphthol, cyclohexanol, 2-methyl-1-pentanol (2M1P), 4-methyl-2-pentanol (4M2P), benzene and toluene. Equilibrium adsorption of various probe compounds on the coals were measured with the inverse liquid chromatography method. Experiments on flotation of various 60-200 mesh treated coals such as Illinois {number_sign}6 coal (PSOC-1539), Adaville {number_sign}1 coal (PSOC-1544), Wyodak coal (PSOC-1545) and Pittsburgh {number_sign}8 coal (PSOC-1549) were performed. The chosen coals were treated with steam, nitrogen and air at 1 atm and 125-225{degrees}C for 24 hours. The coals were treated with water as well as 20-1000 ppm aqueous alcohol solutions for 3-24 hours at 150-225{degrees}C. The coals also were treated with 20-ppm alcohol aqueous solutions for 1-24 hours at the 0.002-g/min mass flow rate of alcohol aqueous solutions and at 225{degrees}C. Flotation experiments were conducted with a 500-cm{sup 3} batch-type micro flotation apparatus, introducing nitrogen at the bottom of the apparatus. This final report was prepared with the experimental data obtained during the period of September 1991-March 1994.

  15. Combination of Liquid Chromatography with Multivariate Curve Resolution-Alternating Least-Squares (MCR-ALS) in the Quantitation of Polycyclic Aromatic Hydrocarbons Present in Paprika Samples.

    PubMed

    Monago-Maraña, Olga; Pérez, Rocío L; Escandar, Graciela M; Muñoz de la Peña, Arsenio; Galeano-Díaz, Teresa

    2016-11-02

    This work presents a strategy for quantitating polycyclic aromatic hydrocarbons (PAHs) in smoked paprika samples. For this, a liquid chromatographic method with fluorimetric detection (HPLC-FLD) was optimized. To resolve some interference co-eluting with the target analytes, the second-order multivariate curve resolution-alternating least-squares (MCR-ALS) algorithm has been employed combined with this liquid chromatographic method. Among the eight PAHs quantified (fluorene, phenanthrene, anthracene, pyrene, chrysene, benzo[a]anthracene, benzo[b]fluoranthene, and benzo[a]pyrene) by HPLC-FLD, only in the case of fluorene, pyrene, and benzo[b]fluoranthene was it necessary to apply the second-order algorithm for their resolution. Limits of detection and quantitation were between 0.015 and 0.45 mg/kg and between 0.15 and 1.5 mg/kg, respectively. Good recovery results (>80%) for paprika were obtained via the complete extraction procedure, consisting of an extraction from the matrix and the cleanup of the extract by means of silica cartridges. Higher concentrations of chrysene, benzo[a]anthracene, benzo[b]fluoranthene, and benzo[a]pyrene were found in the paprika samples, with respect to the maximal amounts allowed for other spices that are under European Regulation (EU) N° 2015/1933.

  16. Optimization of pressurized liquid extraction using a multivariate chemometric approach and comparison of solid-phase extraction cleanup steps for the determination of polycyclic aromatic hydrocarbons in mosses.

    PubMed

    Foan, L; Simon, V

    2012-09-21

    A factorial design was used to optimize the extraction of polycyclic aromatic hydrocarbons (PAHs) from mosses, plants used as biomonitors of air pollution. The analytical procedure consists of pressurized liquid extraction (PLE) followed by solid-phase extraction (SPE) cleanup, in association with analysis by high performance liquid chromatography coupled with fluorescence detection (HPLC-FLD). For method development, homogeneous samples were prepared with large quantities of the mosses Isothecium myosuroides Brid. and Hypnum cupressiforme Hedw., collected from a Spanish Nature Reserve. A factorial design was used to identify the optimal PLE operational conditions: 2 static cycles of 5 min at 80 °C. The analytical procedure performed with PLE showed similar recoveries (∼70%) and total PAH concentrations (∼200 ng g(-1)) as found using Soxtec extraction, with the advantage of reducing solvent consumption by 3 (30 mL against 100mL per sample), and taking a fifth of the time (24 samples extracted automatically in 8h against 2 samples in 3.5h). The performance of SPE normal phases (NH(2), Florisil, silica and activated aluminium) generally used for organic matrix cleanup was also compared. Florisil appeared to be the most selective phase and ensured the highest PAH recoveries. The optimal analytical procedure was validated with a reference material and applied to moss samples from a remote Spanish site in order to determine spatial and inter-species variability. Copyright © 2012 Elsevier B.V. All rights reserved.

  17. The physics of coal liquid slurry atomization. Final report to Department of Energy - PETC

    SciTech Connect

    Chigier, N.; Mansour, A.

    1995-10-01

    The stability of turbulent columns of liquid injected into a quiescent environment was studied. Laser Doppler Anemometry measurements of the flow patterns and turbulence characteristics in free liquid jets were made. Turbulence decay along Newtonian jets was investigated along with the effects of turbulence on the resulting droplet size distributions after breakup. The rate of decay of turbulence properties along the jet were investigated. Disintegration of liquid jets injected into a high-velocity gas stream has also been studied. Newtonian and non-Newtonian liquids were studied with particular emphasis on the non-Newtonian rheological characteristics. Determination was made of the extent that the addition of high molecular weight polymer to liquids change the breakup process. Shear thinning, extension thinning and extension thickening fluids were investigated. Shear viscosities were measured over five decades of shear rates. The contraction flow technique was also used for measurement of the extensional viscosity of non-Newtonian liquids. The die-swell technique was also used to determine the first normal stress difference. The near field produced by a co-axial airblast atomizer was investigated using the phase Doppler particle analyzer. Whether or not the classical wave mechanism and empirical models reported for airblast atomization of low viscosity liquid are applicable to airblast atomization of viscous non-Newtonian liquids was determined. The theoretical basis of several models which give the best fit to the experimental data for airblast atomization of non-Newtonian liquids was also discussed. The accuracy of the wave mechanism-based models in predicting droplets sizes after breakup of viscous non-Newtonian liquids using an airblast atomizer has also been demonstrated.

  18. Comparative study for determination of some polycyclic aromatic hydrocarbons ‘PAHs' by a new spectrophotometric method and multivariate calibration coupled with dispersive liquid-liquid extraction

    NASA Astrophysics Data System (ADS)

    Abdel-Aziz, Omar; El Kosasy, A. M.; El-Sayed Okeil, S. M.

    2014-12-01

    A modified dispersive liquid-liquid extraction (DLLE) procedure coupled with spectrophotometric techniques was adopted for simultaneous determination of naphthalene, anthracene, benzo(a)pyrene, alpha-naphthol and beta-naphthol in water samples. Two different methods were used, partial least-squares (PLS) method and a new derivative ratio method, namely extended derivative ratio (EDR). A PLS-2 model was established for simultaneous determination of the studied pollutants in methanol, by using twenty mixtures as calibration set and five mixtures as validation set. Also, in methanol a novel (EDR) method was developed for determination of the studied pollutants, where each component in the mixture of the five PAHs was determined by using a mixture of the other four components as divisor. Chemometric and EDR methods could be also adopted for determination of the studied PAH in water samples after transferring them from aqueous medium to the organic one by utilizing dispersive liquid-liquid extraction technique, where different parameters were investigated using a full factorial design. Both methods were compared and the proposed method was validated according to ICH guidelines and successfully applied to determine these PAHs simultaneously in spiked water samples, where satisfactory results were obtained. All the results obtained agreed with those of published methods, where no significant difference was observed.

  19. Comparative study for determination of some polycyclic aromatic hydrocarbons 'PAHs' by a new spectrophotometric method and multivariate calibration coupled with dispersive liquid-liquid extraction.

    PubMed

    Abdel-Aziz, Omar; El Kosasy, A M; El-Sayed Okeil, S M

    2014-12-10

    A modified dispersive liquid-liquid extraction (DLLE) procedure coupled with spectrophotometric techniques was adopted for simultaneous determination of naphthalene, anthracene, benzo(a)pyrene, alpha-naphthol and beta-naphthol in water samples. Two different methods were used, partial least-squares (PLS) method and a new derivative ratio method, namely extended derivative ratio (EDR). A PLS-2 model was established for simultaneous determination of the studied pollutants in methanol, by using twenty mixtures as calibration set and five mixtures as validation set. Also, in methanol a novel (EDR) method was developed for determination of the studied pollutants, where each component in the mixture of the five PAHs was determined by using a mixture of the other four components as divisor. Chemometric and EDR methods could be also adopted for determination of the studied PAH in water samples after transferring them from aqueous medium to the organic one by utilizing dispersive liquid-liquid extraction technique, where different parameters were investigated using a full factorial design. Both methods were compared and the proposed method was validated according to ICH guidelines and successfully applied to determine these PAHs simultaneously in spiked water samples, where satisfactory results were obtained. All the results obtained agreed with those of published methods, where no significant difference was observed.

  20. Measurement of muon plus proton final states in νμ interactions on hydrocarbon at < Eν > = 4.2 GeV

    SciTech Connect

    Walton, T.

    2015-04-01

    A study of charged-current muon neutrino scattering on hydrocarbon in which the final state includes a muon, at least one proton, and no pions is presented. Although this signature has the topology of neutrino quasielastic scattering from neutrons, the event sample contains contributions from quasielastic and inelastic processes where pions are absorbed in the nucleus. The analysis accepts events with muon production angles up to 70° and proton kinetic energies greater than 110 MeV. The cross section, when based completely on hadronic kinematics, is well described by a relativistic Fermi gas nuclear model including the neutrino event generator modeling for inelastic processes and particle transportation through the nucleus. This is in contrast to the quasielastic cross section based on muon kinematics, which is best described by an extended model that incorporates multinucleon correlations. As a result, this measurement guides the formulation of a complete description of neutrino-nucleus interactions that encompasses the hadronic as well as the leptonic aspects of this process.

  1. Measurement of muon plus proton final states in νμ interactions on hydrocarbon at < Eν > = 4.2 GeV

    DOE PAGES

    Walton, T.

    2015-04-01

    A study of charged-current muon neutrino scattering on hydrocarbon in which the final state includes a muon, at least one proton, and no pions is presented. Although this signature has the topology of neutrino quasielastic scattering from neutrons, the event sample contains contributions from quasielastic and inelastic processes where pions are absorbed in the nucleus. The analysis accepts events with muon production angles up to 70° and proton kinetic energies greater than 110 MeV. The cross section, when based completely on hadronic kinematics, is well described by a relativistic Fermi gas nuclear model including the neutrino event generator modeling formore » inelastic processes and particle transportation through the nucleus. This is in contrast to the quasielastic cross section based on muon kinematics, which is best described by an extended model that incorporates multinucleon correlations. As a result, this measurement guides the formulation of a complete description of neutrino-nucleus interactions that encompasses the hadronic as well as the leptonic aspects of this process.« less

  2. Magnetic microsphere-confined graphene for the extraction of polycyclic aromatic hydrocarbons from environmental water samples coupled with high performance liquid chromatography-fluorescence analysis.

    PubMed

    Wang, Weina; Ma, Ruiyang; Wu, Qiuhua; Wang, Chun; Wang, Zhi

    2013-06-07

    In this paper, a magnetic microsphere-confined graphene adsorbent (Fe3O4@SiO2-G) was fabricated and used for the extraction of five polycyclic aromatic hydrocarbons (fluorene, anthracene, phenanthrene, fluoranthene and pyrene) from environmental water samples prior to high performance liquid chromatography with fluorescence detection. The Fe3O4@SiO2-G was characterized by various instrumental methods. Various experimental parameters that could affect the extraction efficiencies, such as the amount of Fe3O4@SiO2-G, the pH and ionic strength of sample solution, the extraction time and the desorption conditions, were investigated. Due to the high surface area and excellent adsorption capacity of the Fe3O4@SiO2-G, satisfactory extraction can be achieved with only 15mg of the adsorbent per 250mL solution and 5min extraction. Under the optimum conditions, a linear response was observed in the concentration range of 5-1500ngL(-1) for fluorene, 2.5-1500ngL(-1) for anthracene and 15-1500ngL(-1) for phenanthrene, fluoranthene and pyrene, with the correlation coefficients (r) ranging from 0.9897 to 0.9961. The limits of detection (S/N=3) of the method were between 0.5 and 5.0ngL(-1). The relative standard deviations (RSDs) were less than 5.6%. The recoveries of the method were in the range between 83.2% and 108.2%. The results indicated that this graphene-based magnetic nanocomposite had a great adsorptive ability toward the five polycyclic aromatic hydrocarbons from environmental water samples.

  3. Hydrogen production by reforming of liquid hydrocarbons in a membrane reactor for portable power generation-Model simulations

    NASA Astrophysics Data System (ADS)

    Damle, Ashok S.

    One of the most promising technologies for lightweight, compact, portable power generation is proton exchange membrane (PEM) fuel cells. PEM fuel cells, however, require a source of pure hydrogen. Steam reforming of hydrocarbons in an integrated membrane reactor has potential to provide pure hydrogen in a compact system. In a membrane reactor process, the thermal energy needed for the endothermic hydrocarbon reforming may be provided by combustion of the membrane reject gas. The energy efficiency of the overall hydrogen generation is maximized by controlling the hydrogen product yield such that the heat value of the membrane reject gas is sufficient to provide all of the heat necessary for the integrated process. Optimization of the system temperature, pressure and operating parameters such as net hydrogen recovery is necessary to realize an efficient integrated membrane reformer suitable for compact portable hydrogen generation. This paper presents results of theoretical model simulations of the integrated membrane reformer concept elucidating the effect of operating parameters on the extent of fuel conversion to hydrogen and hydrogen product yield. Model simulations indicate that the net possible hydrogen product yield is strongly influenced by the efficiency of heat recovery from the combustion of membrane reject gas and from the hot exhaust gases. When butane is used as a fuel, a net hydrogen recovery of 68% of that stoichiometrically possible may be achieved with membrane reformer operation at 600 °C (873 K) temperature and 100 psig (0.791 MPa) pressure provided 90% of available combustion and exhaust gas heat is recovered. Operation at a greater pressure or temperature provides a marginal improvement in the performance whereas operation at a significantly lower temperature or pressure will not be able to achieve the optimal hydrogen yield. Slightly higher, up to 76%, net hydrogen recovery is possible when methanol is used as a fuel due to the lower heat

  4. Laser-induced back-side etching with liquid and the solid hydrocarbon absorber films of different thicknesses

    NASA Astrophysics Data System (ADS)

    Ehrhardt, M.; Lorenz, P.; Yunxiang, P.; Bayer, L.; Han, B.; Zimmer, K.

    2017-04-01

    Laser-induced backside wet and dry etching (LIBWE and LIBDE) are methods for high-quality surface patterning of transparent dielectrics that making use of an additional absorber material attached to the rear side that is ablated in a confined configuration. Due to the manifold of the involved processes, the mechanism of the etching process and the parameter influence on the material removal process are multifaceted and not fully understood yet. In the present paper, we investigate the influence of the confinement to the backside etching process by studying the impact of the thickness of the attached liquid or solid absorber within a range of 12-125 and 0.2-11.7 μm, respectively. It was found that for the liquid and solid absorbers, the etching rate increases with the thickness of the absorber layer and saturates exceeding a certain value, which depends on the used laser fluence. Moreover, the incubation of etching depends on the absorber thickness. The comparison of the etching results of a similar thickness of the liquid and the solid absorber layers shows that the phase of the absorber (liquid or solid) does not influence the back-side etching process. Time-resolved shadowgraph images of the process indicate that with higher absorber layer thickness, the interaction time and strength of the laser-induced processes at the sample surface increase. The results suggest that confinement of the rear side attached absorber ablation influences the impact of the laser-induced secondary processes to the strength of the material modifications and, therefore, the etching rate.

  5. A Final Year Physics Undergraduate Experiment on Ultrasound Propagation in Liquids.

    ERIC Educational Resources Information Center

    van der Sluijs, M. J.; van der Sluijs, J. C. A.

    1980-01-01

    Describes an advanced undergraduate physics experiment which permits the measurement of ultrasound velocity and absorption in liquid systems. A description of the tasks the student is expected to perform is also included. (HM)

  6. Polyurethane foam chips combined with liquid chromatography in the determination of unmetabolized polycyclic aromatic hydrocarbons excreted in human urine.

    PubMed

    Buratti, Marina; Pellegrino, Oronzo; Valla, Carla; Rubino, Federico Maria; Verduci, Cinzia; Colombi, Antonio

    2006-09-01

    A method suitable for the determination of unmetabolized polycyclic aromatic hydrocarbons (PAHs) excreted at trace levels (ng/L) in human urine for the monitoring of exposure of the general population to PAH contamination was developed. PAHs were determined, after enrichment by solid-phase extraction on polyurethane foam (PUF) chips, by HPLC with fluorescence detection. Different parameters affecting analyte extraction to the PUF, including urine salting-out and organic additives, and optimization of conditions for clean-up and desorption have been investigated. Optimized conditions were 40 mL acidified urine sample, added with magnesium sulfate, tetrahydrofuran and a 2 cm3 PUF chip, and extracted by shaking at 30 rpm for 1 h at ambient temperature. Desorption was performed, after a clean-up step with diluted sodium hydroxide, using a small amount of diethyl ether. The recovery of PAH congeners from spiked urines was >90% in the 2-100 ng/L range; the detection limit was 0.1-0.5 ng/L, depending on the considered PAH congener; day-to-day precision, at 50 ng/L native PAH content, was CV = 10-20%. The proposed technique provides a simple, economical and effective procedure for the determination of trace amounts of unmetabolized PAHs excreted in human urine spot samples.

  7. Biomass conversion to produce hydrocarbon liquid fuel via hot-vapor filtered fast pyrolysis and catalytic hydrotreating

    DOE PAGES

    Wang, Huamin; Elliott, Douglas C.; French, Richard J.; ...

    2016-12-25

    Lignocellulosic biomass conversion to produce biofuels has received significant attention because of the quest for a replacement for fossil fuels. Among the various thermochemical and biochemical routes, fast pyrolysis followed by catalytic hydrotreating is considered to be a promising near-term opportunity. This paper reports on experimental methods used 1) at the National Renewable Energy Laboratory (NREL) for fast pyrolysis of lignocellulosic biomass to produce bio-oils in a fluidized-bed reactor and 2) at Pacific Northwest National Laboratory (PNNL) for catalytic hydrotreating of bio-oils in a two-stage, fixed-bed, continuous-flow catalytic reactor. The configurations of the reactor systems, the operating procedures, and themore » processing and analysis of feedstocks, bio-oils, and biofuels are described in detail in this paper. We also demonstrate hot-vapor filtration during fast pyrolysis to remove fine char particles and inorganic contaminants from bio-oil. Representative results showed successful conversion of biomass feedstocks to fuel-range hydrocarbon biofuels and, specifically, the effect of hot-vapor filtration on bio-oil production and upgrading. As a result, the protocols provided in this report could help to generate rigorous and reliable data for biomass pyrolysis and bio-oil hydrotreating research.« less

  8. Biomass Conversion to Produce Hydrocarbon Liquid Fuel Via Hot-vapor Filtered Fast Pyrolysis and Catalytic Hydrotreating

    PubMed Central

    Wang, Huamin; Elliott, Douglas C.; French, Richard J.; Deutch, Steve; Iisa, Kristiina

    2016-01-01

    Lignocellulosic biomass conversion to produce biofuels has received significant attention because of the quest for a replacement for fossil fuels. Among the various thermochemical and biochemical routes, fast pyrolysis followed by catalytic hydrotreating is considered to be a promising near-term opportunity. This paper reports on experimental methods used 1) at the National Renewable Energy Laboratory (NREL) for fast pyrolysis of lignocellulosic biomass to produce bio-oils in a fluidized-bed reactor and 2) at Pacific Northwest National Laboratory (PNNL) for catalytic hydrotreating of bio-oils in a two-stage, fixed-bed, continuous-flow catalytic reactor. The configurations of the reactor systems, the operating procedures, and the processing and analysis of feedstocks, bio-oils, and biofuels are described in detail in this paper. We also demonstrate hot-vapor filtration during fast pyrolysis to remove fine char particles and inorganic contaminants from bio-oil. Representative results showed successful conversion of biomass feedstocks to fuel-range hydrocarbon biofuels and, specifically, the effect of hot-vapor filtration on bio-oil production and upgrading. The protocols provided in this report could help to generate rigorous and reliable data for biomass pyrolysis and bio-oil hydrotreating research. PMID:28060311

  9. Biomass conversion to produce hydrocarbon liquid fuel via hot-vapor filtered fast pyrolysis and catalytic hydrotreating

    SciTech Connect

    Wang, Huamin; Elliott, Douglas C.; French, Richard J.; Deutch, Steve; Iisa, Kristiina

    2016-12-25

    Lignocellulosic biomass conversion to produce biofuels has received significant attention because of the quest for a replacement for fossil fuels. Among the various thermochemical and biochemical routes, fast pyrolysis followed by catalytic hydrotreating is considered to be a promising near-term opportunity. This paper reports on experimental methods used 1) at the National Renewable Energy Laboratory (NREL) for fast pyrolysis of lignocellulosic biomass to produce bio-oils in a fluidized-bed reactor and 2) at Pacific Northwest National Laboratory (PNNL) for catalytic hydrotreating of bio-oils in a two-stage, fixed-bed, continuous-flow catalytic reactor. The configurations of the reactor systems, the operating procedures, and the processing and analysis of feedstocks, bio-oils, and biofuels are described in detail in this paper. We also demonstrate hot-vapor filtration during fast pyrolysis to remove fine char particles and inorganic contaminants from bio-oil. Representative results showed successful conversion of biomass feedstocks to fuel-range hydrocarbon biofuels and, specifically, the effect of hot-vapor filtration on bio-oil production and upgrading. As a result, the protocols provided in this report could help to generate rigorous and reliable data for biomass pyrolysis and bio-oil hydrotreating research.

  10. Biomass Conversion to Produce Hydrocarbon Liquid Fuel Via Hot-vapor Filtered Fast Pyrolysis and Catalytic Hydrotreating.

    PubMed

    Wang, Huamin; Elliott, Douglas C; French, Richard J; Deutch, Steve; Iisa, Kristiina

    2016-12-25

    Lignocellulosic biomass conversion to produce biofuels has received significant attention because of the quest for a replacement for fossil fuels. Among the various thermochemical and biochemical routes, fast pyrolysis followed by catalytic hydrotreating is considered to be a promising near-term opportunity. This paper reports on experimental methods used 1) at the National Renewable Energy Laboratory (NREL) for fast pyrolysis of lignocellulosic biomass to produce bio-oils in a fluidized-bed reactor and 2) at Pacific Northwest National Laboratory (PNNL) for catalytic hydrotreating of bio-oils in a two-stage, fixed-bed, continuous-flow catalytic reactor. The configurations of the reactor systems, the operating procedures, and the processing and analysis of feedstocks, bio-oils, and biofuels are described in detail in this paper. We also demonstrate hot-vapor filtration during fast pyrolysis to remove fine char particles and inorganic contaminants from bio-oil. Representative results showed successful conversion of biomass feedstocks to fuel-range hydrocarbon biofuels and, specifically, the effect of hot-vapor filtration on bio-oil production and upgrading. The protocols provided in this report could help to generate rigorous and reliable data for biomass pyrolysis and bio-oil hydrotreating research.

  11. Biomass Conversion to Produce Hydrocarbon Liquid Fuel Via Hot-vapor Filtered Fast Pyrolysis and Catalytic Hydrotreating

    SciTech Connect

    Wang, Huamin; Elliott, Douglas C.; French, Richard J.; Deutch, Steve; Iisa, Kristiina

    2016-01-01

    Lignocellulosic biomass conversion to produce biofuels has received significant attention because of the quest for a replacement for fossil fuels. Among the various thermochemical and biochemical routes, fast pyrolysis followed by catalytic hydrotreating is considered to be a promising near-term opportunity. This paper reports on experimental methods used 1) at the National Renewable Energy Laboratory (NREL) for fast pyrolysis of lignocellulosic biomass to produce bio-oils in a fluidized-bed reactor and 2) at Pacific Northwest National Laboratory (PNNL) for catalytic hydrotreating of bio-oils in a two-stage, fixed-bed, continuous-flow catalytic reactor. The configurations of the reactor systems, the operating procedures, and the processing and analysis of feedstocks, bio-oils, and biofuels are described in detail in this paper. We also demonstrate hot-vapor filtration during fast pyrolysis to remove fine char particles and inorganic contaminants from bio-oil. Representative results showed successful conversion of biomass feedstocks to fuel-range hydrocarbon biofuels and, specifically, the effect of hot-vapor filtration on bio-oil production and upgrading. The protocols provided in this report could help to generate rigorous and reliable data for biomass pyrolysis and bio-oil hydrotreating research.

  12. Determination of oxygenated and native polycyclic aromatic hydrocarbons in urban dust and diesel particulate matter standard reference materials using pressurized liquid extraction and LC-GC/MS.

    PubMed

    Ahmed, Trifa M; Bergvall, Christoffer; Åberg, Magnus; Westerholm, Roger

    2015-01-01

    The objective of this study was to develop a novel analytical chemistry method, comprised of a coupled high-performance liquid chromatography-gas chromatography/mass spectrometry system (LC-GC/MS) with low detection limits and high selectivity, for the identification and determination of oxygenated polycyclic aromatic hydrocarbons (OPAHs) and polycyclic aromatic hydrocarbons (PAHs) in urban air and diesel particulate matter. The linear range of the four OPAHs, which include 9,10-anthraquinone, 4H-cyclopenta[def]phenanthrene-4-one, benzanthrone, and 7,12-benz[a]anthraquinone, was 0.7 pg-43.3 ng with limits of detection (LODs) and limits of quantification (LOQs) on the order of 0.2-0.8 and 0.7-1.3 pg, respectively. The LODs in this study are generally lower than values reported in the literature, which can be explained by using large-volume injection. The recoveries of the OPAHs spiked onto glass fiber filters using two different pressurized liquid extraction (PLE) methods were in the ranges of 84-107 and 67-110 %, respectively. The analytical protocols were validated using the following National Institute of Standards and Technology standard reference materials: SRM 1649a (Urban Dust), SRM 1650b (Diesel Particulate Matter), and SRM 2975 (Diesel Particulate Matter, Industrial Forklift). The measured mass fractions of the OPAHs in the standard reference materials (SRMs) in this present study are higher than the values from the literature, except for benzanthrone in SRM 1649a (Urban Dust). In addition to the OPAHs, 44 PAHs could be detected and quantified from the same particulate extract used in this protocol. Using data from the literature and applying a two-sided t test at the 5 % level using Bonferroni correction, significant differences were found between the tested PLE methods for individual PAHs. However, the measured mass fractions of the PAHs were comparable, similar to, or higher than those previously reported in the literature.

  13. Fast automated dual-syringe based dispersive liquid-liquid microextraction coupled with gas chromatography-mass spectrometry for the determination of polycyclic aromatic hydrocarbons in environmental water samples.

    PubMed

    Guo, Liang; Tan, Shufang; Li, Xiao; Lee, Hian Kee

    2016-03-18

    An automated procedure, combining low density solvent based solvent demulsification dispersive liquid-liquid microextraction (DLLME) with gas chromatography-mass spectrometry analysis, was developed for the determination of polycyclic aromatic hydrocarbons (PAHs) in environmental water samples. Capitalizing on a two-rail commercial autosampler, fast solvent transfer using a large volume syringe dedicated to the DLLME process, and convenient extract collection using a small volume microsyringe for better GC performance were enabled. Extraction parameters including the type and volume of extraction solvent, the type and volume of dispersive solvent and demulsification solvent, extraction and demulsification time, and the speed of solvent injection were investigated and optimized. Under the optimized conditions, the linearity ranged from 0.1 to 50 μg/L, 0.2 to 50 μg/L, and 0.5 to 50 μg/L, depending on the analytes. Limits of detection were determined to be between 0.023 and 0.058 μg/L. The method was applied to determine PAHs in environmental water samples.

  14. Liquid-vapor and solid-liquid-vapor equilibrium in natural gas systems. Final report, January 1983-December 1985

    SciTech Connect

    Sloan, E.D.; Kidnay, A.J.

    1985-10-01

    The three-phase (SLV) equilibria for the methane + carbon dioxide system was measured at 206, 208, 210, 212, 214, and 216 K, and a complete isotherm was determined at 212 K. The ethane + carbon dioxide system was studied at 204, 206, 208, 209, 210, 212, 213, 214, 216 K and complete isotherms determined at 204, 207, 209, 210, 212, and 216 K. The propane + carbon dioxide system was studied at 208, 210, 212, 214, and 216 K with a complete isotherm measured at 216 K. Preliminary data on temperature, pressure, and mole fraction at the triple points are tabulated. Vapor liquid equilibria data are presented for the ethane + carbon dioxide system at 207, 210, 220, 223.15, 230, 250, 263.15, 270, 213, 230, 250, and 270 K. Binary interaction parameters were fit for the Soave-Redlich-Kwong equation of state. VLE measurements are presented for the nitrogen + ethane, and the nitrogen + carbon dioxide system at 220 K and 270 K. Measurements are also presented for the ternary system nitrogen + carbon dioxide + ethane at 220 K and at three pressures ranging from the pressure of 0.803 (the carbon dioxide + ethane azeotrope) to 9 MPa.

  15. 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.

  16. 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.

  17. Final Technical Report, Grant DE-FG02-87ER13714, "Fundamental Studies of Metastable Liquids"

    SciTech Connect

    Pablo G. Debenedetti

    2009-03-09

    Grant DE-FG02-87ER13714 supported fundamental work on the physical properties of metastable liquids from 6/1/87 to 4/30/08. Renewal proposals were submitted every three years (1990, 1993, 1996, 1999, 2002, 2005), and included, in every case, a detailed Final Technical Report on the previous three years. Accordingly, the bulk of this report covers the final 2-year period 5/1/06 to 4/30/08 of this grant, which is not covered in any of the previous Final Technical Reports. This is preceded by a brief overview of the main research objectives and principal accomplishments during these very fruitful and productive 21 years of DOE-funded research.

  18. Three-dimensional ionic liquid functionalized magnetic graphene oxide nanocomposite for the magnetic dispersive solid phase extraction of 16 polycyclic aromatic hydrocarbons in vegetable oils.

    PubMed

    Zhang, Yun; Zhou, Hua; Zhang, Zhe-Hua; Wu, Xiang-Lun; Chen, Wei-Guo; Zhu, Yan; Fang, Chun-Fu; Zhao, Yong-Gang

    2017-03-17

    In this paper, a novel three-dimensional ionic liquid functionalized magnetic graphene oxide nanocomposite (3D-IL@mGO) was prepared, and used as an effective adsorbent for the magnetic dispersive solid phase extraction (MSPE) of 16 polycyclic aromatic hydrocarbons (PAHs) in vegetable oil prior to gas chromatography-mass spectrometry (GC-MS). The properties of 3D-IL@mGO were characterized by scanning electron micrographs (SEM), X-ray photoelectron spectroscopy (XPS), vibrating sample magnetometer (VSM). The 3D-IL@mGO, functionalized by ionic liquid, exhibited high adsorption toward PAHs. Compared to molecularly imprinted solid phase extraction (MISPE), the MSPE method based on 3D-IL@mGO had less solvent consumption and low cost, and was more efficent to light PAHs in quantitative analysis. Furthermore, the rapid and accurate GC-MS method coupled with 3D-IL@mGO MSPE procedure was successfully applied for the analysis of 16 PAHs in eleven vegetable oil samples from supermarket in Zhejiang Province. The results showed that the concentrations of BaP in 3 out of 11 samples were higher than the legal limit (2.0μg/kg, Commission Regulation 835/2011a), the sum of 8 heavy PAHs (BaA, CHR, BbF, BkF, BaP, IcP, DaA, BgP) in 11 samples was between 3.03μg/kg and 229.5μg/kg. Validation results on linearity, specificity, accuracy, precision and stability, as well as on application to the analysis of PAHs in oil samples demonstrated the applicability to food safety risk monitoring in China. Copyright © 2017 Elsevier B.V. All rights reserved.

  19. Final Report Full-Scale Test of DWPF Advanced Liquid-Level and Density Measurement Bubblers

    SciTech Connect

    Duignan, M.R.; Weeks, G.E.

    1999-07-01

    As requested by the Technical Task Request (1), a full-scale test was carried out on several different liquid-level measurement bubblers as recommended from previous testing (2). This final report incorporates photographic evidence (Appendix B) of the bubblers at different stages of testing, along with the preliminary results (Appendix C) which were previously reported (3), and instrument calibration data (Appendix D); while this report contains more detailed information than previously reported (3) the conclusions remain the same. The test was performed under highly prototypic conditions from November 26, 1996 to January 23, 1997 using the full-scale SRAT/SME tank test facilities located in the 672-T building at TNX. Two different types of advanced bubblers were subjected to approximately 58 days of slurry operation; 14 days of which the slurry was brought to boiling temperatures.The test showed that the large diameter tube bubbler (2.64 inches inside diameter) operated successfully throughout the2-month test by not plugging with the glass-frit ladened slurry which was maintained at a minimum temperature of 50 deg Cand several days of boiling temperatures. However, a weekly blow-down with air or water is recommended to minimize the slurry which builds up.The small diameter porous tube bubbler (0.62 inch inside diameter; water flow {gt} 4 milliliters/hour = 1.5 gallons/day) operated successfully on a daily basis in the glass-frit ladened slurry which was maintained at a minimum temperature of 50 degrees C and several days of boiling temperatures. However, a daily blow-down with air, or air and water, is necessary to maintain accurate readings.For the small diameter porous tube bubbler (0.62 inch inside diameter; water flow {gt} 4 milliliters/hour = 1.5 gallons/day) there were varying levels of success with the lower water-flow tubes and these tubes would have to be cleaned by blowing with air, or air and water, several times a day to maintain them plug free. This

  20. ICPP radioactive liquid and calcine waste technologies evaluation final report and recommendation

    SciTech Connect

    1995-04-01

    Using a formalized Systems Engineering approach, the Latched Idaho Technologies Company developed and evaluated numerous alternatives for treating, immobilizing, and disposing of radioactive liquid and calcine wastes at the Idaho Chemical Processing Plant. Based on technical analysis data as of March, 1995, it is recommended that the Department of Energy consider a phased processing approach -- utilizing Radionuclide Partitioning for radioactive liquid and calcine waste treatment, FUETAP Grout for low-activity waste immobilization, and Glass (Vitrification) for high-activity waste immobilization -- as the preferred treatment and immobilization alternative.

  1. Commercial polymeric fiber as sorbent for solid-phase microextraction combined with high-performance liquid chromatography for the determination of polycyclic aromatic hydrocarbons in water.

    PubMed

    Hii, Toh Ming; Basheer, Chanbasha; Lee, Hian Kee

    2009-10-30

    A novel microextraction method making use of commercial polymer fiber as sorbent, coupled with high-performance liquid chromatography-fluorescence detection for the determination of polycyclic aromatic hydrocarbons (PAHs) in water has been developed. In this technique, the extraction device was simply a length (8 cm) of a strand of commercial polymer fiber, Kevlar (each strand consisted of 1000 filaments, each of diameter ca. 9.23 microm), that was allowed to tumble freely in the aqueous sample solution during extraction. The extracted analytes were desorbed ultrasonically before the extract was injected into HPLC system for analysis. Extraction parameters such as extraction time, desorption time, type of desorption solvent and sample volume were optimized. Each fiber could be used for up to 50 extractions and the method showed good precision, reproducibility and linear response within a concentration range 0.05-5.00 microg L(-1) with correlation coefficients of up to 0.9998. Limits of detection between 0.4 and 4.4 ng L(-1) for seven PAHs could be achieved. The relative standard deviations (n=3) of this technique were between 2.9% and 12.1%.

  2. Magnetic nanoparticles-carbon nanotubes hybrid composites for selective solid-phase extraction of polycyclic aromatic hydrocarbons and determination by ultra-high performance liquid chromatography.

    PubMed

    Corps Ricardo, Ana I; Guzmán Bernardo, Francisco J; Zougagh, Mohammed; Rodríguez Martín-Doimeadios, Rosa C; Ríos, Ángel

    2017-08-01

    A rapid and reliable method based on magnetic solid-phase extraction (MSPE) and ultra-high performance liquid chromatography (UHPLC-FLD) analysis was developed and validated for the quantitative determination of seven polycyclic aromatic hydrocarbons (PAHs) in water samples. Hybrid composites made up of magnetic nanoparticles (MNPs) and carbon nanotubes (CNTs) were tested as adsorbent materials. The main factors influencing the extraction yields were optimized, namely the amount and type of adsorbent in the adsorption, and the solvent, the type of energy and the time in the desorption step. The selected composite was made up of Fe3O4 and multiwalled (MW)-CNTs. The desorption was carried out with sonication probe and tetrahydrofuran (THF); this solvent makes the method directly compatible with the chromatographic mobile phase and it reduces the analysis time. Under the optimized conditions, the LODs and LOQs achieved were in the range of 0.025-0.73 and 0.04-2.4 ng mL(-1), respectively. The calibration curves were linear (R (2) ≥ 0.9936) over the concentration ranges from 1 to 500 ng mL(-1). The recoveries of PAHs were from 76.4 ± 1.7 up to 106.5 ± 3.5%. The method was applied to synthetic and real (tap, dam, river and mineral) water samples with different characteristics to evaluate the performance under real conditions.

  3. Two-liquid-phase system: A promising technique for predicting bioavailability of polycyclic aromatic hydrocarbons in long-term contaminated soils.

    PubMed

    Wang, Congying; Wang, Ziyu; Li, Zengbo; Ahmad, Riaz

    2017-02-01

    A two-liquid-phase system (TLPS), which consisted of soil slurry and silicone oil, was employed to extract polycyclic aromatic hydrocarbons (PAHs) in four long-term contaminated soils in order to assess the bioavailability of PAHs. Extraction kinetics of six PAHs viz. phenanthrene, fluoranthene, pyrene, benzo(a)anthracene, benzo(a)pyrene, dibenzo(a,h)anthrancene were selected to investigate as they covered the susceptible and recalcitrant PAHs in soil. A parallel experiments were also carried out on the microbial degradation of these PAHs in soil with and without biostimulation (by adding (NH4)2HPO4). The rapidly desorbed fraction of fluoranthene, as indicated by the two-fraction model, was found the highest, ranging from 21.4% to 37.4%, whereas dibenzo(a,h)anthrancene was the lowest, ranging from 8.9% to 20.5%. The rapid desorption of selected PAHs was found to be finished within 24 h. The rapidly desorbed fraction of PAHs investigated using TLPS, was significantly correlated (R(2) = 0.95) with that degraded by microorganisms in biostimulation treatment. This suggested that the TLPS-assisted extraction could be a promising technique in determining the bioavailability of aged PAHs in contaminated soils. It also suggested that applying sufficient nutrients in bioremediation of field contaminated soils is crucial. Further work is required to test its application to more hydrophobic organic pollutants in long-term contaminated soils. Copyright © 2016 Elsevier Ltd. All rights reserved.

  4. Analysis of EU priority polycyclic aromatic hydrocarbons in food supplements using high performance liquid chromatography coupled to an ultraviolet, diode array or fluorescence detector.

    PubMed

    Danyi, Sophie; Brose, François; Brasseur, Catherine; Schneider, Yves-Jacques; Larondelle, Yvan; Pussemier, Luc; Robbens, Johan; De Saeger, Sarah; Maghuin-Rogister, Guy; Scippo, Marie-Louise

    2009-02-09

    High performance liquid chromatography coupled to an ultraviolet, diode array or fluorescence detector (HPLC/UV-FLD) has been used to set up a method to detect the 15(+1) EU priority polycyclic aromatic hydrocarbons (PAHs) in food supplements covering the categories of dried plants and plant extracts excluding oily products. A mini validation was performed and the following parameters have been determined: limit of detection, limit of quantification, precision, recovery and linearity. They were in close agreement with quality criteria described in the Commission Regulation (EC) No 333/2007 concerning the PAH benzo[a]pyrene in foodstuffs, except the not fluorescent cyclopenta[c,d]pyrene for which the UV detection leads to a higher limit of detection. Analysis of twenty commercial food supplements covering mainly the class of dried plants was performed to evaluate their PAHs contamination levels and to test the applicability of the method to various plant matrices. Fifty percent of analyzed samples showed concentration exceeding 2 microgkg(-1) for one or more PAHs.

  5. Tuning the selectivity of polymeric ionic liquid sorbent coatings for the extraction of polycyclic aromatic hydrocarbons using solid-phase microextraction.

    PubMed

    Meng, Yunjing; Anderson, Jared L

    2010-10-01

    A new generation polymeric ionic liquid (PIL), poly(1-4-vinylbenzyl)-3-hexadecylimidazolium bis[(trifluoromethyl)sulfonyl]imide (poly(VBHDIm(+) NTf(2)(-))), was synthesized and is shown to exhibit impressive selectivity towards the extraction of 12 polycyclic aromatic hydrocarbons (PAHs) from aqueous samples when used as a sorbent coating in direct-immersion solid-phase microextraction (SPME) coupled to gas chromatography (GC). The PIL was imparted with aromatic character to enhance π-π interactions between the analytes and the sorbent coating. For comparison purposes, a PIL with similar structure but lacking the π-π interaction capability, poly(1-vinyl-3-hexadecylimidazolium bis[(trifluoromethyl)sulfonyl]imide) (poly(HDIm(+) NTf(2)(-))), as well as a commercial polydimethylsiloxane (PDMS) sorbent coating were evaluated and exhibited much lower extraction efficiencies. Extraction parameters, including stir rate and extraction time, were studied and optimized. The detection limits of poly(VBHDIm(+) NTf(2)(-)), poly(HDIm(+) NTf(2)(-)), and PDMS coatings varied between 0.003-0.07 μg L(-1), 0.02-0.6 μg L(-1), and 0.1-6 μg L(-1), respectively. The partition coefficients (logK(fs)) of eight PAHs to the three studied fiber coatings were estimated using a static SPME approach. This study represents the first report of analyte partition coefficients to any PIL-based material.

  6. Highly sensitive copper fiber-in-tube solid-phase microextraction for online selective analysis of polycyclic aromatic hydrocarbons coupled with high performance liquid chromatography.

    PubMed

    Sun, Min; Feng, Juanjuan; Bu, Yanan; Luo, Chuannan

    2015-08-21

    A fiber-in-tube solid-phase microextraction (SPME) device was developed with copper wire and copper tube, which was served as both the substrate and sorbent with high physical strength and good flexibility. Its morphology and surface properties were characterized by scanning electron microscopy and energy dispersive X-ray spectrometry. It was coupled with high performance liquid chromatography (HPLC) equipment by replacing the sample loop of six-port injection valve, building the online SPME-HPLC system conveniently. Using ten polycyclic aromatic hydrocarbons (PAHs) as model analytes, extraction conditions including sampling rate, extraction time, organic content and desorption time were investigated and optimized. The copper fiber-in-tube exhibits excellent extraction efficiency toward PAHs, with enrichment factors from 268 to 2497. The established online SPME-HPLC method provides good linearity (0.05-100μgL(-1)) and low detection limits (0.001-0.01μgL(-1)) for PAHs. It has been used to determine PAHs in water samples, with recoveries in the range of 86.2-115%. Repeatability on the same extraction tube is in the range of 0.6-3.6%, and repeatability among three tubes is in the range of 5.6-20.1%. Compared with phthalates, anilines and phenols, the copper fiber-in-tube possesses good extraction selectivity for PAHs. The extraction mechanism is probably related to hydrophobic interaction and π-electron-metal interaction.

  7. Fast analysis of 29 polycyclic aromatic hydrocarbons (PAHs) and nitro-PAHs with ultra-high performance liquid chromatography-atmospheric pressure photoionization-tandem mass spectrometry

    PubMed Central

    Lung, Shih-Chun Candice; Liu, Chun-Hu

    2015-01-01

    Polycyclic aromatic hydrocarbons (PAHs) and nitro-PAHs are ubiquitous in the environment. Some of them are probable carcinogens and some are source markers. This work presents an ultra-high performance liquid chromatography-atmospheric pressure photoionization-tandem mass spectrometry (UHPLC-APPI-MS/MS) method for simultaneous analysis of 20 PAHs and nine nitro-PAHs. These compounds are separated in 15 minutes in the positive mode and 11 minutes in the negative mode, one half of GC/MS analysis time. Two pairs of precursor/product ions are offered, which is essential for confirmation. This method separates and quantifies benzo[a]pyrene (the most toxic PAHs) and non-priority benzo[e]pyrene (isomers, little toxicity) to avoid overestimation of toxin levels, demonstrating its importance for health-related researches. With 0.5% 2,4-difluoroanisole in chlorobenzene as the dopant, limits of detection of PAHs except acenaphthylene and those of nitro-PAHs except 2-nitrofluoranthene are below 10 pg and 3 pg, respectively, mostly lower than or comparable to those reported using LC-related systems. The responses were linear over two orders of magnitude with fairly good accuracy and precision. Certified reference materials and real aerosol samples were analyzed to demonstrate its applicability. This fast, sensitive, and reliable method is the first UHPLC-APPI-MS/MS method capable of simultaneously analyzing 29 environmentally and toxicologically important PAHs and nitro-PAHs. PMID:26265155

  8. One-step solvent extraction followed by liquid chromatography-atmospheric pressure photoionization tandem mass spectrometry for the determination of polycyclic aromatic hydrocarbons in edible oils.

    PubMed

    Shi, Long-Kai; Liu, Yu-Lan; Liu, Hua-Min; Zhang, Ming-Ming

    2015-05-01

    A method for rapid analysis of 16 polycyclic aromatic hydrocarbons (PAHs) in edible oils has been developed on the basis of a simplified solvent extraction and liquid chromatography-atmospheric pressure photoionization tandem mass spectrometry performed in multiple reaction monitoring mode. The briefness of the experimental procedure, the use of milliliters of acetonitrile for extraction without any further cleanup process, the short analysis time, and the excellent sensitivity and selectivity demonstrated the advantages of this practical and environmentally friendly method. All the analytes exhibited satisfactory recoveries at three spiking levels (the recoveries ranged from 77.8 to 106.4%), and the relative standard deviations were lower than 10%. The limits of quantitation of this method for the 16 PAHs were in the range of 0.02-0.43 μg/kg. The validated method was successfully applied for the determination of PAHs in coconut oil reference material (BCR-458) and real edible oil samples. The results suggested that a large-scale investigation of the concentration of PAHs in vegetable oils in China is required.

  9. Triphenylamine-functionalized magnetic microparticles as a new adsorbent coupled with high performance liquid chromatography for the analysis of trace polycyclic aromatic hydrocarbons in aqueous samples.

    PubMed

    Long, Yiming; Chen, Yingzhuang; Yang, Fei; Chen, Chunyan; Pan, Di; Cai, Qingyun; Yao, Shouzhuo

    2012-06-07

    Triphenylamine (TPA)-functionalized magnetic microspheres (Fe(3)O(4)/SiO(2)/TPA) were prepared and applied as solid phase extraction (SPE) adsorbents for the analysis of polycyclic aromatic hydrocarbons (PAHs) in environmental samples in combination with high-performance liquid chromatography (HPLC). The magnetic solid-phase extraction (MSPE) conditions affecting the extraction efficiency were optimized, including elution solvent, standing time, amount of sorbent, and salt concentration. Due to the strong π-π conjugate effect between the benzene rings of TPA and PAHs, high extraction efficiency was achieved with spiked recoveries of 80.21-108.33% and relative standard deviations (RSD) of less than 10%. Good linearities (R(2) > 0.997) for all calibration curves were obtained with low limits of detection (LOD) of 0.25, 0.5, 0.5, 3.75, 0.2 and 0.04 ng L(-1) for anthracene, fluoranthene, pyrene, chrysene, benzo[b]fluoranthene and benzo[k]fluoranthene, respectively. The achieved results indicate the applicability of Fe(3)O(4)/SiO(2)/TPA as MSPE adsorbents.

  10. Fast analysis of 29 polycyclic aromatic hydrocarbons (PAHs) and nitro-PAHs with ultra-high performance liquid chromatography-atmospheric pressure photoionization-tandem mass spectrometry.

    PubMed

    Lung, Shih-Chun Candice; Liu, Chun-Hu

    2015-08-12

    Polycyclic aromatic hydrocarbons (PAHs) and nitro-PAHs are ubiquitous in the environment. Some of them are probable carcinogens and some are source markers. This work presents an ultra-high performance liquid chromatography-atmospheric pressure photoionization-tandem mass spectrometry (UHPLC-APPI-MS/MS) method for simultaneous analysis of 20 PAHs and nine nitro-PAHs. These compounds are separated in 15 minutes in the positive mode and 11 minutes in the negative mode, one half of GC/MS analysis time. Two pairs of precursor/product ions are offered, which is essential for confirmation. This method separates and quantifies benzo[a]pyrene (the most toxic PAHs) and non-priority benzo[e]pyrene (isomers, little toxicity) to avoid overestimation of toxin levels, demonstrating its importance for health-related researches. With 0.5% 2,4-difluoroanisole in chlorobenzene as the dopant, limits of detection of PAHs except acenaphthylene and those of nitro-PAHs except 2-nitrofluoranthene are below 10 pg and 3 pg, respectively, mostly lower than or comparable to those reported using LC-related systems. The responses were linear over two orders of magnitude with fairly good accuracy and precision. Certified reference materials and real aerosol samples were analyzed to demonstrate its applicability. This fast, sensitive, and reliable method is the first UHPLC-APPI-MS/MS method capable of simultaneously analyzing 29 environmentally and toxicologically important PAHs and nitro-PAHs.

  11. Retentivity, selectivity and thermodynamic behavior of polycyclic aromatic hydrocarbons on charge-transfer and hypercrosslinked stationary phases under conditions of normal phase high performance liquid chromatography.

    PubMed

    Jiang, Ping; Lucy, Charles A

    2016-03-11

    Charge-transfer and hypercrosslinked polystyrene phases offer retention and separation for polycyclic aromatic hydrocarbons (PAHs) and thus have potential for petroleum analysis. The size, shape and planarity selectivity for PAH standards on charge-transfer (DNAP column) and hypercrosslinked polystyrene (HC-Tol and 5HGN columns) phases are different under normal phase liquid chromatography (NPLC). The HC-Tol column behaves like a conventional NPLC column with low retention of PAHs. Retention of PAHs on the DNAP and 5HGN are strong and increases with the number of aromatic rings. The main retention mechanism is through π-π interactions and dipole-induced dipole interaction. Thermodynamics indicates that the retention mechanism of PAHs remains unchanged over the temperature range 20-60°C. In addition, on either DNAP or 5HGN column, both linear and bent PAHs are retained through the same mechanism. But DNAP possesses smaller π-π interaction and higher planarity selectivity than 5HGN for PAHs. This is suggestive that DNAP interacts with PAHs through a disordered phase arrangement, while 5HGN behaves as an ordered adsorption phase. Copyright © 2016 Elsevier B.V. All rights reserved.

  12. A new strategy based on cholesterol-functionalized iron oxide magnetic nanoparticles for determination of polycyclic aromatic hydrocarbons by high-performance liquid chromatography with cholesterol column.

    PubMed

    Yan, Zhihong; Yuan, Jinbin; Zhu, Genhua; Zou, Ying; Chen, Chunyan; Yang, Shaolei; Yao, Shouzhuo

    2013-05-30

    This study reported for the first time the use of cholesterol-functionalized magnetic nanoparticles (Fe3O4@SiO2@Chol) for the determination of polycyclic aromatic hydrocarbons (PAHs) in traditional Chinese medicine samples (TCMs) by high performance liquid chromatography (HPLC) coupled with fluorescence detection. The method was efficient, environmentally friendly, and fast. The solvent consumption of the proposed column is only half of the conventional column but with higher efficiency. Influencing factors, including sorbent amount, desorption solvent, sample volume and extraction time, were investigated in detail. Under the optimum conditions, good linearity (R(2)>0.991) was obtained over the range of 5-400 ng g(-1), with limits of detection (LOD) 0.75, 0.50, 1.0, 0.56, 0.60, 0.84 and 0.80 ng g(-1) for anthracene, fluoranthene, pyrene, chrysene, benzo[a]anthracene, benzo(b)fluoranthene and benzo(k)fluoranthene, respectively. Crown Copyright © 2013. Published by Elsevier B.V. All rights reserved.

  13. Fast analysis of 29 polycyclic aromatic hydrocarbons (PAHs) and nitro-PAHs with ultra-high performance liquid chromatography-atmospheric pressure photoionization-tandem mass spectrometry

    NASA Astrophysics Data System (ADS)

    Lung, Shih-Chun Candice; Liu, Chun-Hu

    2015-08-01

    Polycyclic aromatic hydrocarbons (PAHs) and nitro-PAHs are ubiquitous in the environment. Some of them are probable carcinogens and some are source markers. This work presents an ultra-high performance liquid chromatography-atmospheric pressure photoionization-tandem mass spectrometry (UHPLC-APPI-MS/MS) method for simultaneous analysis of 20 PAHs and nine nitro-PAHs. These compounds are separated in 15 minutes in the positive mode and 11 minutes in the negative mode, one half of GC/MS analysis time. Two pairs of precursor/product ions are offered, which is essential for confirmation. This method separates and quantifies benzo[a]pyrene (the most toxic PAHs) and non-priority benzo[e]pyrene (isomers, little toxicity) to avoid overestimation of toxin levels, demonstrating its importance for health-related researches. With 0.5% 2,4-difluoroanisole in chlorobenzene as the dopant, limits of detection of PAHs except acenaphthylene and those of nitro-PAHs except 2-nitrofluoranthene are below 10 pg and 3 pg, respectively, mostly lower than or comparable to those reported using LC-related systems. The responses were linear over two orders of magnitude with fairly good accuracy and precision. Certified reference materials and real aerosol samples were analyzed to demonstrate its applicability. This fast, sensitive, and reliable method is the first UHPLC-APPI-MS/MS method capable of simultaneously analyzing 29 environmentally and toxicologically important PAHs and nitro-PAHs.

  14. Thermocatalytic CO{sub 2}-Free Production of Hydrogen from Hydrocarbon Fuels - Final Report for the Period August 1999 - September 2000

    SciTech Connect

    Nazim Muradov, Ph.D.

    2000-10-01

    The overall objective of this work is to develop a novel process for CO{sub 2}-free production of hydrogen via thermocatalytic decomposition (pyrolysis) of hydrocarbon fuels as a viable alternative to the conventional processes of methane steam reforming or partial oxidation. The objective of Phase I work was to demonstrate the technical feasibility of CO{sub 2}-free production of hydrogen and carbon from different hydrocarbons, including methane, propane and gasoline.

  15. Direct determination of polynuclear aromatic hydrocarbons in coal liquids and shale oil by laser excited Shpol'skii spectrometry

    SciTech Connect

    Yen, Y.; D'Silva, A.P.; Fassel, V.A.; Iles, M.

    1980-07-01

    This article reports that tunable, dye laser excitation of Shpol'skii effect spectra provides a potentially useful means of determining PAH compounds directly in coal liquids and shale oil without prior isolation of the PAH fraction by chromatographic or other techniques. The data reported were obtained by selecting excitation wavelengths within the response curve of a single dye, 2-(4-biphenylyl)-5-phenyl-1,3,4 oxadiazole (PBD). The characteristic low temperature excitation spectra of PAH compounds in appropriate Shpol'skii matrices are known to be sharp (FWHM approx. 10cm/sup -1/). The luminescence of four individual PAHs is included. The analytical results obtained for a typical solvent refined coal and shale oil sample are summarized. 2 figures, 1 table. (DP)

  16. High performance liquid chromatographic hydrocarbon group-type analyses of mid-distillates employing fuel-derived fractions as standards

    NASA Technical Reports Server (NTRS)

    Seng, G. T.; Otterson, D. A.

    1983-01-01

    Two high performance liquid chromatographic (HPLC) methods have been developed for the determination of saturates, olefins and aromatics in petroleum and shale derived mid-distillate fuels. In one method the fuel to be analyzed is reacted with sulfuric acid, to remove a substantial portion of the aromatics, which provides a reacted fuel fraction for use in group type quantitation. The second involves the removal of a substantial portion of the saturates fraction from the HPLC system to permit the determination of olefin concentrations as low as 0.3 volume percent, and to improve the accuracy and precision of olefins determinations. Each method was evaluated using model compound mixtures and real fuel samples.

  17. Liquid-Phase Deposition of CIS Thin Layers: Final Report, February 2003--July 2005

    SciTech Connect

    Ernst, F.; Pirouz, P.

    2006-02-01

    The goal of this project was to fabricate single-phase CIS (a-Cu-In-Se, stoichiometric composition: CuInSe2) thin films for photovoltaic applications from a liquid phase - a Cu-In-Se melt of appropriate composition. This approach of liquid-phase deposition (LPD) is based on the new phase diagram we have established for Cu-In-Se, the first complete equilibrium phase diagram of this system. The liquidus projection exhibits four composition fields in which the primary solid phase, i.e., the first solid material that forms on cooling down from an entirely liquid state, is a-CuInSe2. Remarkably, none of the four composition fields is anywhere near the stoichiometric composition (CuInSe2) of a-CuInSe2. The results demonstrate that the proposed technique is indeed capable of producing films with a particularly large grain size and a correspondingly low density of grain boundaries. To obtain films sufficiently thin for solar cell applications and with a sufficiently smooth surface, it is advantageous to employ a sliding boat mechanism. Future work on liquid-phase deposition of CIS should focus on the interaction between the melt and the substrate surface, the resulting CIS interfaces, the surface morphology of the LPD-grown films, and, of course, the electronic properties of the material.

  18. A STUDY OF HOW A CHILD LEARNS CONCEPTS ABOUT CHARACTERISTICS OF LIQUID MATERIALS. FINAL REPORT.

    ERIC Educational Resources Information Center

    ENGELMANN, SIEGFRIED; GALLAGHER, JAMES J.

    THE PURPOSE OF THE STUDY WAS TO EXPLORE THE PIAGET CONCEPT OF CONSERVATION WITH REGARD TO THE CHILD'S CONCEPT OF THE PROPERTY OF LIQUIDS. AN INVESTIGATOR-CONSTRUCTED CONSERVATION INVENTORY WAS GIVEN TO 45 KINDERGARTEN AND FIRST GRADE PUPILS SELECTED FROM THE PRAIRIE ELEMENTARY SCHOOLS, URBANA, ILLINOIS, TO PROVIDE AN INDEX OF THE CHILD'S…

  19. Solar-chemical energy conversion via reversible liquid phase Diels-Alder reactions. Final technical report

    SciTech Connect

    Lenz, T.G.; Hegedus, L.S.; Vaughan, J.D.

    1983-05-01

    Thermochemical energy conversion at moderate or low temperature (< about 400/sup 0/C) employing liquid phase components throughout a cycle is suggested as a promising concept for high-efficiency conversion of solar energy to a convenient chemical form. In particular, we propose liquid phase Diels-Alder cycloaddition chemistry as an important class of reversible reactions for such low or moderate temperature thermochemical energy conversion systems. One of the important attributes of thermally driven Diels-Alder reactions is their concerted mechanism, with consequent high yields and efficiencies relative to liquid photochemical systems. Since the systems we propose involve organic species, with thermal stability concerns about 400/sup 0/C, it is important to demonstrate equilibrium shift capability for the highly energetic reactions sought. We have therefore carried out experimental studies with model liquid Diels-Alder systems that clearly demonstrate the degree of control over equilibrium available through substituent entropy effects. These results are of importance as regards subsequent systematic identification of Diels-Alder reactions having ideal thermochemical and physical properties.

  20. Grazing incidence liquid metal mirrors (GILMM) as the final optics for laser inertial fusion energy power plants

    SciTech Connect

    Moir, R W

    1999-06-25

    A thin film of liquid metal serves as a grazing incident liquid metal mirror (GILMM) for robust final optics of an inertial fusion energy (IFE) power plant. The amount of laser light the mirror can withstand, called the damage limit, of a sodium film 85{degree} from normal arbitrarily set by surface temperature rise of 200 C to limit liquid ablation is 57 J/cm{sup 2} normal to the beam for a 20 ns pulse and 1.3 J/cm{sup 2} for a 10 ps pulse of 0.35 pm light. Liquid aluminum can handle 106 J/cm{sup 2}. The damage limit actually should be set by avoiding liquid ablation due to the rapid surface heating which is expected to result in even higher temperatures rises than 200 C and even higher power densities. The liquid surface is kept flat to the required accuracy by a combination of polished substrate, adaptive optics, surface tension and low Reynolds number, laminar flow in the film. The film's substrate must be polished to {+-}0.015 m. Then surface tension keeps the surface smooth over short distances (<10 mm) and low Reynolds number laminar flow keeps the surface smooth by keeping the film thickness constant to less than {+-} 0.01 pm over long distance >10 mm. Adaptive (deformable) optics techniques keep the substrate flat to within {+-}0.06 {micro}m over 100 mm distance and {+-}0.6 {micro}m over 1,000 mm distances. The mirror can withstand the x-ray pulse when located 30 m away from the microexplosions of nominal yield of 400 MJ (50 MJ x rays) when Li is used but for higher atomic number liquids like Na and Al there may be too high a temperature rise forcing use of other x-ray attenuation methods such as xenon gas, which may be needed for first wall protecting anyway. The cumulative damage from neutrons causing warpage of the liquid film's substrate can be compensated by adaptive optics techniques giving the mirrors long life, perhaps 30 years. The GILMM should be applicable to both direct and indirect drive and pulse lengths appropriate to slow compression

  1. Hydrotreating of a Lurgi coal liquid. Phase one. Final report, June 1, 1978-December 31, 1979

    SciTech Connect

    Wilson, D.B.; Conners, R.W.

    1980-07-01

    Coal liquids produced during the gasification of coal via the Lurgi Process were hydrotreated to determine whether sulfur, nitrogen and oxygen could be removed leaving a liquid product suitable for high grade use, e.g. refinery feed or chemicals. The experimental system was a semi-batch (continuous gas flow) stirred, slurry reactor. A commercial nickel-molybdenum catalyst was used which required presulfiding prior to hydrotreating. The reaction system was operated at 360 psig and at temperatures of 275, 300 and 325/sup 0/C. Product analysis was by gas chromatography. Qualitative determination of ammonia (primary denitrogenation product) and water (primary deoxygenation product) was made. Quantitative determination of hydrogen sulfide was performed. The lumped kinetics desulfurization reactions were pseudo first order with an apparent activation energy 14.500 Kcal/g mole.

  2. Liquid-phase methanation/shift process development. Final technical report, September 1, 1980-November 30, 1981

    SciTech Connect

    Not Available

    1982-05-12

    This final technical report covers the work performed between September 1, 1980 and November 30, 1981 relating to Chem Systems' Liquid Phase Methanation/Shift Process. A total of 44 runs were completed covering testing of five commercially available catalysts at 900/sup 0/F, 1000 psig and 10,000 h/sup -1/ VHSV. The shifted methanation feed gas consisted of 63% H/sub 2/, 19% CO, 2% CO/sub 2/ and 16% CH/sub 4/. To determine the effects of steam, twenty of the scans had 15% steam injected into the feed gas. Each test ran for 100, 300, 600 or 1200 hours with continuous effluent sampling and temperature profile monitoring. At each of the termination points, a catalyst sample was taken from the hot spot section of the bed for analysis. Carbon was deposited on the catalyst under the methanation conditions studied. The rate of carbon deposition was primarily a function of catalyst properties and not of the thermodynamics of the methanation reaction system. In spite of heavy carbon deposition, the catalytic behavior for these systems generally remains unaffected. Physical plugging of the catalyst bed is the limiting condition of the process and not catalyst deactivation. In this respect, a controlled oxidation of the carbon deposits is a viable method of extending catalyst life. The hydrodynamics and design of a cold-flow test unit for a three-phase, liquid-fluidized bed for Liquid Phase Methanation/Shift was evaluated. The cold-flow unit process design, equipment take-off lists, consruction cost and timing schedule are included. As a second potential application, the unit was designed for hydrodynamic studies of a liquid-entrained system for Liquid Phase Methanation/Shift.

  3. Solidification Technologies for Radioactive and Chemical Liquid Waste Treatment - Final CRADA Report

    SciTech Connect

    Castiglioni, Andrew J.; Gelis, Artem V.

    2016-01-01

    This project, organized under DOE/NNSA's Global Initiatives for Proliferation Prevention program, joined Russian and DOE scientists in developing more effective solidification and storage technologies for liquid radioactive waste. Several patent applications were filed by the Russian scientists (Russia only) and in 2012, the technology developed was approved by Russia's Federal State Unitary Enterprise RADON for application throughout Russia in cleaning up and disposing of radioactive waste.

  4. Enrichment of light hydrocarbon mixture

    DOEpatents

    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.

  5. Enrichment of light hydrocarbon mixture

    SciTech Connect

    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.

  6. Beaufort Sea monitoring program: analysis of trace metals and hydrocarbons from Outer Continental Shelf (OCS) activities. Final report, 1983-1986

    SciTech Connect

    Boehm, P.D.; Crecelius, E.; Steinhauer, W.; Steinhauer, M.; Tuckfield, C.

    1986-08-13

    An environmental-monitoring program, designed to detect and quantify long-term changes in sediment and tissue concentrations of metals and hydrocarbons potentially due to oil and gas exploration and development on the U.S. Beaufort Sea continental shelf, was initiated in 1984. In Year-1 of the three-year study, a series of benthic stations was established in the nearshore area between Barter Island and Cape Halkett. In Year-2 of the study, areal coverage of the Study Area was increased to 39 marine stations and 10 shoreline and river stations. Analysis of six replicate sediment samples for trace metals, and saturated and aromatic hydrocarbons revealed a wide range of concentrations. Both trace metal and hydrocarbon analyses of bivalve and crustacean tissues indicated concentrations differences between species but no apparent relationship between animal body burdens and sediment concentrations.

  7. Fate and transport of particle-reactive normal, alkylated and heterocyclic aromatic hydrocarbons in a sediment-water-colloid system. University research initiative. Final report

    SciTech Connect

    Means, J.C.; McMillin, D.J.

    1993-06-01

    The overall study framework is designed to investigate the fate, transport and chemical transformations of normal, alkylated and heterocyclic aromatic hydrocarbons associated with spilled oil, operational discharges and produced water discharges in coastal marine and estuarine environmental systems. In the present research, the nature of the particle reactivity or sorption/desorption equilibria which control the fate, transport and chemical transformations of hydrocarbons has been investigated throgh studies of the sorption/desorption equilibria and kinetics of selected normal, alkylated and heterocyclic PAH on various sediment types (a range of organic carbon and particle sizes) over a range of salinities and studies of the relationship between the carbon fraction of sediments and the equilibrium K(suboc) (Partition coefficient) for selected normal, alkylated and heterocyclic PAH. New trace analytical techniques for aromatic hydrocarbons were developed and applied.

  8. Baffin Island experimental oil spill and dispersant studies. Hydrocarbon bioaccumulation and histopathological and biochemical responses in marine bivalve molluscs. Final report

    SciTech Connect

    Neff, J.M.; Hillman, R.E.; Boehm, P.D.

    1984-02-01

    Infaunal bivalve molluscs from four bays at the BIOS experimental oil-spill site became contaiminated with petroleum hydrocarbons. A Lagomedio crude oil and the dispersant, Corexit 9527, were used in these field experiments. Based on chemical data, both Mya and Serripes depurated oil during the two-week post-spill period, in part through an in vivo biodegradation presumably by microbial activity in the guts of the animals. However, Serripes pregerentially retained the high-molucular-weight saturated hydrocarbon assemblage as well as the higher alkylated naphthalene, phenanthrene and dibenzothiophene compounds, whereas Mya depurated all hydrocarbon components although the water-soluble alkyl benzenes and naphthalenes were depurated somewhat faster. However, the deposit feeders continued to accumulate oil from the sediments, at least for the two weeks after the spill.

  9. FINAL REPORT: Room Temperature Hydrogen Storage in Nano-Confined Liquids

    SciTech Connect

    VAJO, JOHN

    2014-06-12

    DOE continues to seek solid-state hydrogen storage materials with hydrogen densities of ≥6 wt% and ≥50 g/L that can deliver hydrogen and be recharged at room temperature and moderate pressures enabling widespread use in transportation applications. Meanwhile, development including vehicle engineering and delivery infrastructure continues for compressed-gas hydrogen storage systems. Although compressed gas storage avoids the materials-based issues associated with solid-state storage, achieving acceptable volumetric densities has been a persistent challenge. This project examined the possibility of developing storage materials that would be compatible with compressed gas storage technology based on enhanced hydrogen solubility in nano-confined liquid solvents. These materials would store hydrogen in molecular form eliminating many limitations of current solid-state materials while increasing the volumetric capacity of compressed hydrogen storage vessels. Experimental methods were developed to study hydrogen solubility in nano-confined liquids. These methods included 1) fabrication of composites comprised of volatile liquid solvents for hydrogen confined within the nano-sized pore volume of nanoporous scaffolds and 2) measuring the hydrogen uptake capacity of these composites without altering the composite composition. The hydrogen storage capacities of these nano-confined solvent/scaffold composites were compared with bulk solvents and with empty scaffolds. The solvents and scaffolds were varied to optimize the enhancement in hydrogen solubility that accompanies confinement of the solvent. In addition, computational simulations were performed to study the molecular-scale structure of liquid solvent when confined within an atomically realistic nano-sized pore of a model scaffold. Confined solvent was compared with similar simulations of bulk solvent. The results from the simulations were used to formulate a mechanism for the enhanced solubility and to guide the

  10. Wavelength tunable liquid crystal imaging filters for remote sensing from geosynchronous platforms. Final Report

    SciTech Connect

    Foukal, P.

    1992-10-01

    Recent advances in liquid crystal technology have enabled us to construct tunable birefringent filters with bandwidths between approximately 0.1 nm and 50 nm. The center wavelength of these filters can be selected electronically, in a few tens of milliseconds, with no moving parts. These liquid crystal tunable filters (LCTF's), together with existing CCD detectors, make possible a new generation of lightweight, rugged, high-resolution imaging spectrophotometers. Such instruments would be particularly interesting for remote sensing applications from geosynchronous platforms. Important advantages exist in the aperture, absence of image shift, power consumption, size, weight, and absence of high drive frequencies, compared to current instruments used or considered for multispectral scene analysis. In the present work, we have reviewed spectral requirements of planned NASA geosynchronous remote sensing missions and identified several applications of the liquid crystal tunable filter technology. We have modeled the LCTF performance in the visible and near-infrared, and carried out a literature study on space-hardening of the filter components, to evaluate the suitability of LCTF's for geosynchronous missions. We have also compared the power consumption, weight, size, reliability, and optical performance of an imaging spectrophotometer using a LCTF monochromator, to other instruments that have been put forward for remote sensing from geosynchronous platforms. We put forward some conceptual designs for LCTF's that seem to offer important reliability, over the mechanical filter wheels presently baselined for the HEPI and ALM experiments. The extremely wide acceptance angle achievable with LCTF's could also avoid the present need for large-aperture interference filters in the ALM (and LIS) experiments. Thermal vacuum testing and radiation damage analysis is required to investigate the space hardening of these new filters for geosynchronous flight.

  11. Development of Liquid Level and Density Bubbler for DWPF Canyon Vessels. Final report

    SciTech Connect

    Duignan, M.R.; Barnes, A.B.

    1994-10-01

    Under Activity No. SRT-ETF-TT-94003-0 (approved March 31, 1994), which is the result of Technical Assistance Request 93-DWPT-PMC-A0002 (issued February 2, 1994), an experiment was performed to test several alternate liquid-level and density measuring bubbler tubes to replace the standard straight tube bubbler sensor used in DWPF canyon vessels and Holledge-type sensors, which are currently in use. This report describes an experiment that elicited positive results from two alternate bubbler tubes that incorporate all of the advantages of the fundamentally simple straight tube bubbler while trying to minimize plugging.

  12. Miniscale Liquid-Liquid Extraction Coupled with Full Evaporation Dynamic Headspace Extraction for the Gas Chromatography/Mass Spectrometric Analysis of Polycyclic Aromatic Hydrocarbons with 4000-to-14 000-fold Enrichment.

    PubMed

    Liew, Christina Shu Min; Li, Xiao; Lee, Hian Kee

    2016-09-20

    A new sample preparation approach of combining a miniscale version of liquid-liquid extraction (LLE), termed miniscale-LLE (msLLE), with automated full evaporation dynamic headspace extraction (FEDHS) was developed. Its applicability was demonstrated in the extraction of several polycyclic aromatic hydrocarbons (PAHs) (acenaphthylene, acenaphthene, fluorene, phenanthrene, anthracene, fluoranthene, and pyrene) from aqueous samples. In the first step, msLLE was conducted with 1.75 mL of n-hexane, and all of the extract was vaporized through a Tenax TA sorbent tube via a nitrogen gas flow, in the FEDHS step. Due to the stronger π-π interaction between the Tenax TA polymer and PAHs, only the latter, and not n-hexane, was adsorbed by the sorbent. This selectivity by the Tenax TA polymer allowed an effective concentration of PAHs while eliminating n-hexane by the FEDHS process. After that, thermal desorption was applied to the PAHs to channel them into a gas chromatography/mass spectrometric (GC/MS) system for analysis. Experimental parameters affecting msLLE (solvent volume and mixing duration) and FEDHS (temperature and duration) were optimized. The obtained results achieved low limits of detection (1.85-3.63 ng/L) with good linearity (r(2) > 0.9989) and high enrichment factors ranging from 4200 to 14 100. The optimized settings were applied to the analysis of canal water sampled from an industrial area and tap water, and this methodology was compared to stir-bar sorptive extraction (SBSE). This innovative combined extraction-concentration approach proved to be fast, effective, and efficient in determining low concentrations of PAHs in aqueous samples.

  13. Characterization and quantification of the hydrocarbons fraction of the subcutaneous fresh fat of Iberian pig by off-line combination of high performance liquid chromatography and gas chromatography.

    PubMed

    Gamero-Pasadas, A; Viera Alcaide, I; Rios, J J; Graciani Constante, E; Vicario, I M; León-Camacho, M

    2006-08-04

    Hydrocarbons in fresh subcutaneous fat of Iberian pig have been analyzed by GC-MS after fractionation of the unsaponifiable fraction with a new off-line combination of HPLC and GC method. The new method proposed improves the recovery and simultaneous quantification of terpenic hydrocarbons in comparison to the traditional LC method. When necessary and for identification purposes, selective ion monitoring (SIM) was used as acquisition mode in GC-MS. To determine the position of the double bonds in the unsaturated hydrocarbon chain the dimethyl disulfide derivatives (DMDS) were obtained. To elucidate the structure of the branched 1-alkenes the hydrocarbon fraction was submitted to hydrogenation. Thirty-five compounds have been identified, including n-alkanes, n-alkenes, branched (n-1,n-2-dimethyl-1-alkenes) and terpenic hydrocarbons, being the most abundant n-alkenes and n-alkanes of even chain of n-C12-n-C26. Besides the hydrocarbons already described in bibliography, a new diterpenic hydrocarbon, ent-kaurene, have been identified for the first time. The compound reported as Neophytadiene by other authors, has been identified as a 20 atoms hydrocarbon with two double bonds, the 7,11,15-trimethyl-heptadeca-1,4-diene.

  14. Dissolution of biological samples in deep eutectic solvents: an approach for extraction of polycyclic aromatic hydrocarbons followed by liquid chromatography-fluorescence detection.

    PubMed

    Helalat-Nezhad, Zahra; Ghanemi, Kamal; Fallah-Mehrjardi, Mehdi

    2015-05-15

    A novel sample preparation method based on the complete dissolution of marine biological samples in choline chloride-oxalic acid (ChCl-Ox) deep eutectic solvent was developed for fast and efficient extraction of eight polycyclic aromatic hydrocarbons (PAHs) using minimum volumes of cyclohexane. The extracted PAHs were purified and then measured by high-performance liquid chromatography-fluorescence detection (HPLC-FL). The effect of key parameters on extraction recoveries and precision was investigated. At optimized conditions, the studied samples were dissolved under atmospheric pressure in ChCl-Ox (1:2) at 55°C for 30min, which is considerably lower than the temperature used in the classical and current methods. After dissolution, it took approximately 20min to quantitatively extract the PAHs from ChCl-Ox using 5mL cyclohexane. Depending on the analyte, the developed method was linear over the calibration range 1.0-250, 2.0-250, and 5.0-250ngg(-1), with r(2)>0.996. The detection limits of the method were between 0.50 and 3.08ngg(-1). The intra-day and inter-day precisions (based on the relative standard deviation, n=5) of the spiked PAHs at a concentration level of 50ngg(-1) were better than 12.6% and 13.3%, respectively. Individual PAH recoveries from spiked marine fish and macroalgae samples were in the range of 71.6% to 109.6%. For comparison, the spiked samples were also subjected to the Soxhlet extraction method. The simplicity of the procedure, high extraction efficiency, short analysis time, and use of safe and inexpensive components suggest the proposed method has a high potential for utilization in routine trace PAH analysis in biological samples.

  15. Thermoelectric-Driven Liquid-Metal Plasma-Facing Structures (TELS) Final Report

    SciTech Connect

    Ruzic, David

    2016-12-17

    The Thermoelectric-Driven Liquid-Metal Plasma-Facing Structures (TELS) project was able to establish the experimental conditions necessary for flowing liquid metal surfaces in order to be utilized as surfaces facing fusion relevant energetic plasma flux. The work has also addressed additional developments along with progressing along the timeline detailed in the proposal. A no-cost extension was requested to conduct other relevant experiment- specifically regarding the characterization droplet ejection during energetic plasma flux impact. A specially designed trench module, which could accommodate trenches with different aspect ratios was fabricated and installed in the TELS setup and plasma gun experiments were performed. Droplet ejection was characterized using high speed image acquisition and also surface mounted probes were used to characterize the plasma. The Gantt chart below had been provided with the original proposal, indicating the tasks to be performed in the third year of funding. These tasks are listed above in the progress report outline, and their progress status is detailed below.

  16. Coal-liquid fuel/diesel engine operating compatibility. Final report

    SciTech Connect

    Hoffman, J.G.; Martin, F.W.

    1983-09-01

    This work is intended to assess the possibilities of using coal-derived liquids (CDL) represented by a specific type (SRC II) and shale-derived distillate fuel in blends of petroleum-derived fuels in medium-speed, high-output, heavy-duty diesel engines. Conclusions are as follows: (1) Blends of solvent refined coal and diesel fuel may be handled safely by experienced diesel engine mechanics. (2) A serious corrosion problem was found in the fuel pump parts when operating with solvent refined coal blended with petroleum. It is expected that a metallurgy change can overcome this problem. (3) Proper selection of materials for the fuel system is required to permit handling coal-derived liquid fuels. (4) A medium speed, high horsepower, 4-cycle diesel engine can be operated on blends of solvent refined coal and petroleum without serious consequences save the fuel system corrosion previously mentioned. This is based on a single, short durability test. (5) As represented by the product evaluated, 100% shale-derived distillate fuel may be used in a medium speed, high horsepower, 4-cycle diesel engine without significant consequences. (6) The shale product evaluated may be blended with petroleum distillate or petroleum residual materials and used as a fuel for medium speed, high horsepower, 4-cycle diesel engines. 7 references, 24 figures, 20 tables.

  17. High throughput liquid and gas chromatography-tandem mass spectrometry assays for tobacco-specific nitrosamine and polycyclic aromatic hydrocarbon metabolites associated with lung cancer in smokers.

    PubMed

    Carmella, Steven G; Ming, Xun; Olvera, Natalie; Brookmeyer, Claire; Yoder, Andrea; Hecht, Stephen S

    2013-08-19

    We developed and applied high throughput liquid and gas chromatography-tandem mass spectrometry (LC-MS/MS and GC-MS/MS) methods for the cigarette smoking-associated biomarkers 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL) and r-1,t-2,3,c-4-tetrahydroxy-1,2,3,4-tetrahydrophenanthrene (PheT), which are urinary metabolites of the carcinogenic tobacco-specific nitrosamine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) and the polycyclic aromatic hydrocarbon phenanthrene. NNAL and PheT levels have been linked to lung cancer in previous studies of smokers. Confirmation of these relationships will require further molecular epidemiology studies, necessitating improved methodology applicable to large numbers of small urine samples. Furthermore, NNAL is excreted in urine either unconjugated or as an N- or O-glucuronide, but little data are available on the amounts of each in urine. For the high throughput analysis of NNAL, 3 aliquots were processed from each urine sample, one for the analysis of free NNAL, one for free NNAL plus NNAL-N-Gluc, and one for total NNAL (the sum of free NNAL, NNAL-N-Gluc, and NNAL-O-Gluc). Ninety-six well plate technology was used for sample enrichment by supported liquid extraction plates, mixed mode reverse-phase/cation exchange solid-phase extraction, and LC-MS/MS analysis. For the analysis of PheT, the urine samples were cleaned up by solid-phase extraction on styrene-divinylbenzene sorbent, silylated, and analyzed by GC-MS/MS, both in 96-well format. The methods were validated analytically with respect to accuracy and precision, and applied in an ongoing molecular epidemiology study of smokers. The amount of total NNAL in smokers' urine was (mean ± SD) 1.65 ± 2.13 pmol/mL (N = 2641). Free NNAL, NNAL-N-Gluc, and NNAL-O-Gluc represented (mean ± SD) 31 ± 11%, 22 ± 14%, and 48 ± 15% of total NNAL, respectively. The amount of PheT in smokers' urine was (mean ± SD) 1.43 ± 2.16 pmol/mL (N = 2613). The methodology described here

  18. Partial oxidation of liquid hydrocarbons in the presence of oxygen-conducting supports: Effect of catalyst layer deposition

    SciTech Connect

    Smith, M.; Berry, D.; Shekhawt, D.; Haynes, D.; Spivey, J.

    2010-01-01

    Ni-substituted barium hexaaluminate (BNHA) catalysts supported onto gadolinium-doped ceria (GDC), an oxygen-conductor, were prepared using two different methods: (1) conventional incipient wetness impregnation (IWI), in which a non-porous GDC support was impregnated in the conventional manner with aqueous precursors, then dried and calcined to form a supported hexaaluminate, and (2) solid-state mixing (SSM), in which solid hexaaluminate and GDC particles were mechanically ground together and thermally treated to produce a final catalyst. These catalysts were compared to bulk, unsupported BNHA; 3 wt% Ni/alumina; and 3 wt% Ni/GDC (the latter two prepared by conventional impregnation) for the partial oxidation (POX) of n-tetradecane. The reaction studies included examining the effect of 50 ppm S as dibenzothiophene (DBT) and 5 wt% 1-methylnaphthalene (MN) on the product yield under POX conditions. Temperature programmed oxidation (TPO) was used to characterize carbon formation in the reactor. The materials were characterized by BET, ICP-OES, XRD, and SEM/EDS prior to the reaction tests. Characterization of the two GDC-supported BNHA catalysts prior to the reaction studies indicated no significant differences in the bulk composition, surface area, and crystal structure. However, SEM images showed a larger amount of exposed GDC support surface area for the material prepared by IWI. Both of the GDC-supported BNHA materials demonstrated greatly reduced deactivation, with significantly reduced carbon formation compared to bulk BNHA. This was attributed to the oxygen-conducting property of the GDC, which reduced the rate of deactivation of the reaction sites by DBT and MN. The material prepared by IWI demonstrated more stable hydrogen and carbon monoxide yield than the material prepared by SSM. Although both catalysts deactivated in the presence of DBT and MN, the activity of the catalyst prepared by IWI recovered activity more quickly after the contaminants were removed

  19. A measurement of the muon neutrino charged current quasielastic-like cross section on a hydrocarbon target and final state interaction effects

    SciTech Connect

    Walton, Tammy

    2014-01-01

    Presented is the analysis of the μ charged-current quasielastic-like interaction with a polystyrene (CH or hydrocarbon) target in the MINER A experiment, which was exposed to a neutrino beam that peaked at 3.5 GeV.

  20. Molecular and biochemical determinants for polynuclear aromatic hydrocarbon biodegradation in the manufactured gas plant soils. Final report, September 1991-June 1992

    SciTech Connect

    Menn, F.M.; Heitzer, A.; Sanseverino, J.; Applegate, B.M.; Ahn, Y.H.

    1992-06-01

    This research was conducted to further the development of new DNA gene probe(s) for quantifying polynuclear aromatic hydrocarbons (PAHs) catabolic bacteria from MGP contaminated soils, and to investigate the use of bioluminescent reporter technology for measuring higher molecular weight PAH(s) degradation, and to examine the role of the naphthalene degradative pathway in degradation of other higher PAHs.

  1. Conserving energy in plastic greenhouses with liquid foam insulation. Final report

    SciTech Connect

    Wells, O.S.

    1980-10-02

    A 25' x 96' quonset-shaped greenhouse, covered with a double layer of polyethylene, was used as a structure for testing the effectiveness of liquid foam as an insulator against night-time heat loss. A foam solution comprised of 3% foam concentrate in water was pumped at 12 to 15 psi through a generator that created bubbles (foam) which filled the space between the two layers. Heat loss reduction varied from 20% to 40% depending upon weather conditions and foaming technique. Antifreeze agents were added to prevent the foam from freezing as it was injected between the layers. Ethylene glycol (at 12%) was the most effective in preventing freezing and also in stabilizing the integrity of the foam.

  2. Development of an extraction process for removal of heteroatoms from coal liquids. Final report

    SciTech Connect

    Not Available

    1994-04-01

    The main goal of this contract was to develop an extraction process for upgrading coal liquids; and in doing so, to reduce the hydrogen requirement in downstream upgrading processes and to yield valuable byproducts. This goal was to be achieved by developing a novel carbon dioxide extraction process for heteroatom removal from coal-derived naphtha, diesel, and jet fuel. The research plan called for the optimization of three critical process variables using a statistically-designed experimental matrix. The commercial potential of the new process was to be evaluated by demonstrating quantitatively the effectiveness of heteroatom removal from three different feedstocks and by conducting a comparative economic analysis of alternate heteroatom removal technologies. Accomplishments are described for the following tasks: food procurement and analysis process variable screening studies; and process assessment.

  3. Studies of momentum and energy transfer across wavy gas-liquid interfaces. Final report

    SciTech Connect

    Dukler, A.E.

    1993-06-01

    Two phase gas-liquid flow and its associated interfaces exist in a wide variety of situations of importance to the Navy and this has prompted the study of the basic flow mechanics which underlie this complex process. The existence of wind-wave interactions over large bodies of water have long been recognized as a special case of two phase flow where the presence of the deformable interface plays a complex role in the generation of waves due to the action of the wind. Less well recognized, but of great importance, are situations of two phase flow which are found in components of power systems such as condensers, boilers refrigeration loops and cryogen lines. Here the characteristics of two phase flow are critical to the reliable design and safe operation of such systems.

  4. Liquid Organic Battery Development: Cooperative Research and Development Final Report, CRADA Number CRD-14-540

    SciTech Connect

    Santhanagopalan, Shriram

    2016-08-01

    Battery electric vehicles (BEV) have the potential to significantly reduce consumption of gasoline and emission of greenhouse gases. However, the commercial success of mass-market, long-range BEVs requires battery technology with a challenging combination of technical metrics -- specific energy, safety, fast recharge capability, cycle life, and cost. The NREL team proposes a robust, liquid-phase battery design utilizing a high-energy organic redox couple capable of decoupling these metrics via electrode exchange to provide the necessary combination of performance characteristics. The overall objective of this project is to demonstrate a functioning prototype and determine its ability to meet RANGE performance targets in large-scale production. Three main tasks described below will work towards this goal with the individual objectives of (1) identifying a robust, high-performance redox couple-solvent-additive combination, (2) designing and demonstrating a functional cell, and (3) analyzing the concept's potential performance and cost in future mass-production scenarios.

  5. Magnetic liquid metal two-phase flow research. Phase 1. Final report

    SciTech Connect

    Graves, R.D.

    1983-04-01

    The Phase I research demonstrates the feasibility of the magnetic liquid metal (MLM) two-phase flow concept. A dispersion analysis is presented based on a complete set of two-phase-flow equations augmented to include stresses due to magnetic polarization of the fluid. The analysis shows that the stability of the MLM two-phase flow is determined by the magnetic Mach number, the slip ratio, geometry of the flow relative to the applied magnetic field, and by the voidage dependence of the interfacial forces. Results of a set of experiments concerned with magnetic effects on the dynamics of single bubble motion in an aqueous-based, viscous, conducting magnetic fluid are presented. Predictions in the theoretical literature are qualitatively verified using a bench-top experimental apparatus. In particular, applied magnetic fields are seen to lead to reduced bubble size at fixed generating orifice pressure.

  6. Microalgae as a source of liquid fuels. Final technical report. [200 references

    SciTech Connect

    Benemann, J.R.; Goebel, R.P.; Weissman, J.C.; Augenstein, D.C.

    1982-05-15

    The economics of liquid-fuels production from microalgae was evaluated. A detailed review of published economic analyses of microalgae biomass production revealed wide variations in the published costs, which ranged from several dollars per pound for existing commercial health-food production in the Far East, to less than .05/lb costs projected for microalgae biomass for fuel conversion. As little design information or specific cost data has been published, a credible cost estimate required the conceptual engineering design and cost estimating of microalgae to liquid-fuels processes. Two systems were analyzed, shallow (2 to 3'') covered ponds and deeper (1 ft) open ponds. Only the latter was selected for an in-depth analysis due to the many technical shortcomings of the former approach. Based on the cost analysis of a very simple and low cost process, the most optimistic costs extrapolated were about $60/barrel. These were based on many optimistic assumptions. Additional, more detailed, engieering and cost analyses would be useful. However, the major emphasis in future work in this area should be on demonstrating the basic premises on which this design was based: high productivity and oil content of microalgae strains that can dominate in open ponds and which can be harvested by a simple bioflocculation process. Several specific basic research needs were identified: (1) Fundamentals of species selection and control in open pond systems. Effects of environmental variables on species dominance is of particular interest. (2) Mechanisms of algae bioflocculation. (3) Photosynthetic pathways and efficiency under conditions of high lipid production. (4) Effects of non-steady state operating conditions, particularly pH (CO/sub 2/ availability), on productivity. 18 figures, 47 tables.

  7. Method for determining asphaltene stability of a hydrocarbon-containing material

    DOEpatents

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

    2013-02-05

    A method for determining asphaltene stability in a hydrocarbon-containing material having solvated asphaltenes therein is disclosed. In at least one embodiment, it involves the steps of: (a) precipitating an amount of the asphaltenes from a liquid sample of the hydrocarbon-containing material with an alkane mobile phase solvent in a column; (b) dissolving a first amount and a second amount of the precipitated asphaltenes by changing the alkane mobile phase solvent to a final mobile phase solvent having a solubility parameter that is higher than the alkane mobile phase solvent; (c) monitoring the concentration of eluted fractions from the column; (d) creating a solubility profile of the dissolved asphaltenes in the hydrocarbon-containing material; and (e) determining one or more asphaltene stability parameters of the hydrocarbon-containing material.

  8. Low Cost Chemical Feedstocks Using an Improved and Energy Efficient Natural Gas Liquid (NGL) Removal Process, Final Technical Report

    SciTech Connect

    Meyer, Howard, S.; Lu, Yingzhong

    2012-08-10

    The overall objective of this project is to develop a new low-cost and energy efficient Natural Gas Liquid (NGL) recovery process - through a combination of theoretical, bench-scale and pilot-scale testing - so that it could be offered to the natural gas industry for commercialization. The new process, known as the IROA process, is based on U.S. patent No. 6,553,784, which if commercialized, has the potential of achieving substantial energy savings compared to currently used cryogenic technology. When successfully developed, this technology will benefit the petrochemical industry, which uses NGL as feedstocks, and will also benefit other chemical industries that utilize gas-liquid separation and distillation under similar operating conditions. Specific goals and objectives of the overall program include: (i) collecting relevant physical property and Vapor Liquid Equilibrium (VLE) data for the design and evaluation of the new technology, (ii) solving critical R&D issues including the identification of suitable dehydration and NGL absorbing solvents, inhibiting corrosion, and specifying proper packing structure and materials, (iii) designing, construction and operation of bench and pilot-scale units to verify design performance, (iv) computer simulation of the process using commercial software simulation platforms such as Aspen-Plus and HYSYS, and (v) preparation of a commercialization plan and identification of industrial partners that are interested in utilizing the new technology. NGL is a collective term for C2+ hydrocarbons present in the natural gas. Historically, the commercial value of the separated NGL components has been greater than the thermal value of these liquids in the gas. The revenue derived from extracting NGLs is crucial to ensuring the overall profitability of the domestic natural gas production industry and therefore of ensuring a secure and reliable supply in the 48 contiguous states. However, rising natural gas prices have dramatically reduced

  9. Grazing incidence liquid metal mirrors (GILMM) for radiation hardened final optics for laser inertial fusion energy power plants

    SciTech Connect

    Moir, R W

    1999-06-30

    A thin film of liquid metal is suggested as a grazing incident liquid metal mirror (GILMM) for robust final optics of a laser inertial fusion energy (IFE) power plant. The amount of laser light the mirror can withstand, called the damage limit, of a sodium film 85{sup o} from normal is calculated to be 57 J/cm{sup 2} normal to the beam for a 20 ns pulse and 1.3 J/cm{sup 2} for a 10 ps pulse of 0.35 {micro}m light (2 m{sup 2} and 90 m{sup 2} of mirror area per 100 kJ of laser energy at 20 ns and 10 ps, respectively). Feasibility relies on keep the liquid surface flat to the required accuracy by a combination of polished substrate, adaptive (deformable) optics, surface tension and low Reynolds number, laminar flow in the film. The film's substrate must be polished to {+-} 0.015 pm. Then surface tension keeps the surface smooth over short distances (<10 mm) and low Reynolds number laminar flow keeps the surface smooth by keeping the film thickness constant to less than + 0.01 w over long distance >10 mm. Adaptive optics techniques keep. the substrate flat to within {+-} 0.06 pm over 100 mm distance and {+-}0.6 {micro}m over 1000 mm distances. The mirror can stand the x-ray pulse when located 30 m away from the microexplosions of nominal yield of 400 MJ (50 MJ of X rays) when Li is used but for higher atomic number liquids like Na there may be too high a temperature rise forcing use of other x-ray attenuation methods such as attenuation by xenon gas. The cumulative damage from neutrons causing warpage of the liquid film's substrate can be compensated by adaptive optics techniques giving the mirrors long life, perhaps 30 years. The GILMM should be applicable to both direct and indirect drive and pulse lengths appropriate to slow compression ({approx}20 ns) or fast ignition ({approx}10 ps). For direct drive laser beams near the poles (70{sup o}, where 90{sup o} is vertical), stable thin films become more challenging. Proof of concept experiments are needed to verify the

  10. Novel macrocyclic carriers for proton-coupled liquid membrane transport. Final report

    SciTech Connect

    Lamb, J.D.; Izatt, R.M.; Bradshaw, J.S.; Shirts, R.B.

    1996-08-24

    The objective of this research program is to elucidate the chemical principles which are responsible for the cation selectivity and permeability of liquid membranes containing macrocyclic carriers. Several new macrocyclic carriers were synthesized during the last three year period. In addition, new, more convenient synthetic routes were achieved for several nitrogen-containing bicyclic and tricyclic macrocycles. The cation binding properties of these macrocycles were investigated by potentiometric titration, calorimetric titration, solvent extraction and NMR techniques. In addition, hydrophobic macrocycles were incorporated into dual hollow fiber and other membrane systems to investigate their membrane performance, especially in the proton-coupled transport mode. A study of the effect of methoxyalkyl macrocycle substituents on metal ion transport was completed. A new calorimeter was constructed which made it possible to study the thermodynamics of macrocycle-cation binding to very high temperatures. Measurements of thermodynamic data for the interaction of crown ethers with alkali and alkaline earth cations were achieved to 473 K. Molecular modeling work was begun for the first time on this project and fundamental principles were identified and developed for the establishment of working models in the future.

  11. Final environmental assessment for the Liquid Phase Methanol (LPMEOH{trademark}) Project

    SciTech Connect

    1995-06-01

    The proposed project is to demonstrate on a commercial scale the production of methanol from coal-derived synthesis gas using the LPMEOH{trademark} process. The methanol produced during this demonstration will be used as a chemical feedstock (on-site) and/or as an alternative fuel in stationary and transportation applications (off-site). In addition, the production of dimethyl ether (DME) as a mixed co-product with methanol may be demonstrated for a six month period under the proposed project pending the results of laboratory/pilot-scale research on scale-up. The DME would be used as fuel in on-site boilers. The proposed LPMEOH facility would occupy approximately 0.6 acres of the 3,890-acre Eastman Chemical facility in Kingsport, TN. The effects of the proposed project include changes in air emissions, wastewater discharge, cooling water discharge, liquid waste quantities, transportation activities, socioeconomic effects, and quantity of solids for disposal. No substantive negative impacts or environmental concerns were identified.

  12. LDRD Final Report - In Operando Liquid Cell TEM Characterization of Nickel-Based Electrocatalyst

    SciTech Connect

    Nielsen, M. H.

    2016-11-07

    A commercial electrochemistry stage for transmission electron microscopy (TEM) was tested to determine whether to purchase one for the microscopes at Lawrence Livermore National Lab (LLNL). Deposition of a nickel-based electrocatalyst was pursued as a material system for the purpose of testing the stage. The stage was found to be problematic with recurring issues in the electrical connections and vacuum sealing, which has thus far precluded a systematic investigation of the original material system. However, the electrochemical cells purchased through this FS will allow the Lawrence Fellow (Nielsen) to continue testing the stage. Furthermore, discussions with a second vendor, which released a similar electrochemical TEM stage during the course of this FS, have resulted in an upcoming longterm loan of their stage at Lawrence Berkeley National Lab (LBNL) for testing. In addition, low-loss electron energy-loss spectroscopy (EELS) measurements on nickel-bearing electrolyte solutions led to a broader EELS investigation of solvents and salt solutions. These measurements form the basis of a manuscript in preparation on EELS measurements of the liquid phase.

  13. Liquid natural gas as a transportation fuel in the heavy trucking industry. Final technical report

    SciTech Connect

    Sutton, W.H.

    1997-06-30

    This report encompasses the second year of a proposed three year project with emphasis focused on fundamental research issues in Use of Liquid Natural Gas as a Transportation Fuel in the Heavy Trucking Industry. These issues may be categorized as (1) direct diesel replacement with LNG fuel, and (2) long term storage/utilization of LNG vent gases produced by tank storage and fueling/handling operation. The results of this work are expected to enhance utilization of LNG as a transportation fuel. The paper discusses the following topics: (A) Fueling Delivery to the Engine, Engine Considerations, and Emissions: (1) Atomization and/or vaporization of LNG for direct injection diesel-type natural gas engines; (2) Fundamentals of direct replacement of diesel fuel by LNG in simulated combustion; (3) Distribution of nitric oxide and emissions formation from natural gas injection; and (B) Short and long term storage: (1) Modification by partial direct conversion of natural gas composition for improved storage characteristics; (2) LNG vent gas adsorption and recovery using activate carbon and modified adsorbents; (3) LNG storage at moderate conditions.

  14. Evaluation of Exxon Donor Solvent (EDS) coal-derived liquid as utility diesel fuel. Final report

    SciTech Connect

    Heater, W.R.; Froh, T.W.; Ariga, S.; Baker, Q.A.; Piispanen, W.; Webb, P.; Trayser, D.; Keane, W.J.

    1983-10-01

    The program consisted of three phases: (I) characterization of the physical and chemical properties of EDS, (II) evaluation of EDS in a laboratory medium-speed diesel engine, and (III) evaluation of EDS in a low-speed diesel engine operating at a utility. The characteristics of high aromatic content and low cetane number that were found during Phase I made it unlikely that EDS could be used as a direct substitute for diesel fuel without engine modification to provide ignition assistance. Phase II was conducted on a 12-cylinder General Electric Company 7FDL diesel engine. Blends of up to 30% EDS and 70% 0.2 diesel fuel (DF-2) were successfully consumed. Dual fuel tests were also conducted on a single cylinder by injecting EDS through the existing engine fuel oil system and injecting DF-2 through an auxiliary nozzle as an ignition source. Acceptable operation was achieved using 5 to 10% pilot oil heat input. Phase III was conducted on a 16-cylinder Cooper-Bessemer LSV-16-GDT diesel engine at an EUC plant in Easton, Maryland. Blends of up to 66.7% EDS and 33.3% DF-2 were successfully consumed. Dual fuel tests were also conducted on a single cylinder by injecting EDS through the existing fuel oil system and using a natural-gas-fueled precombustion chamber as an ignition source. Acceptable operation was achieved using 3 to 6% pilot gas heat input. The program confirmed that it is feasible to consume significant proportions of EDS in a diesel engine, but more development is needed before EDS can be considered a viable alternative liquid fuel for diesel engines, and an industrial hygiene program is needed to assure safe handling of the fuel.

  15. Novel catalysts for upgrading coal-derived liquids. Final technical progress report

    SciTech Connect

    Thompson, L.T.; Savage, P.E.; Briggs, D.E.

    1995-03-31

    Research described in this report was aimed at synthesizing and evaluating supported Mo oxynitrides and oxycarbides for the selective removal of nitrogen, sulfur and oxygen from model and authentic coal-derived liquids. The Al{sub 2}O{sub 3}-supported oxynitrides and oxycarbides were synthesized via the temperature programmed reaction of supported molybdenum oxides or hydrogen bronzes with NH{sub 3} or an equimolar mixture of CH{sub 4} and H{sub 2}. Phase constituents and composition were determined by X-ray diffraction, CHN analysis, and neutron activation analysis. Oxygen chemisorption was used to probe the surface structure of the catalysts. The reaction rate data was collected using specially designed micro-batch reactors. The Al{sub 2}O{sub 3}-supported Mo oxynitrides and oxycarbides were competitively active for quinoline hydrodenitrogenation (HDN), benzothiophene hydrodesulfurization (HDS) and benzofuran hydrodeoxygenation (HDO). In fact, the HDN and HDO specific reaction rates for several of the oxynitrides and oxycarbides were higher than those of a commercial Ni-Mo/Al{sub 2}O{sub 3} hydrotreatment catalyst. Furthermore, the product distributions indicated that the oxynitrides and oxycarbides were more hydrogen efficient than the sulfide catalysts. For HDN and HDS the catalytic activity was a strong inverse function of the Mo loading. In contrast, the benzofuran hydrodeoxygenation (HDO) activities did not appear to be affected by the Mo loading but were affected by the heating rate employed during nitridation or carburization. This observation suggested that HDN and HDS occurred on the same active sites while HDO was catalyzed by a different type of site.

  16. Degradation of mix hydrocarbons by immobilized cells of mix culture using a trickle fluidized bed reactor. Final report: June 1992--June 1994

    SciTech Connect

    Chapatwala, K.D.

    1994-12-01

    The microorganisms capable of degrading mix hydrocarbons were isolated from the soil samples collected from the hydrocarbon contaminated sites. The mix cultures were identified as Pseudomonas acidovorans, Flavobacterium indoltheticum and Phyllobacterium rubiaceum. The bacterial cells of mix cultures were immobilized in calcium-alginate solution in the form of beads. A trickle fluidized bed air-uplift-type reactor designed to study the degradation of mix hydrocarbons was filled with 0.85% normal saline containing the immobilized cells of mix culture. The immobilized beads were aerated with different amounts of CO{sub 2}-free air. The normal saline saturated with BTXs was circulated in the bioreactors at the rate of 2--4 ml/min. The biodegradation of BTXs by the immobilized beads of mix culture was monitored by determining the concentrations of the BTXs and the metabolites formed during their degradation in the samples at regular intervals using GC. The peaks obtained through the degradation of BTXs were not identified and quantified in this study.

  17. Separations of substituted benzenes and polycyclic aromatic hydrocarbons using normal- and reverse-phase high performance liquid chromatography with UiO-66 as the stationary phase.

    PubMed

    Zhao, Wei-Wei; Zhang, Chao-Yan; Yan, Zeng-Guang; Bai, Li-Ping; Wang, Xiayan; Huang, Hongliang; Zhou, You-Ya; Xie, Yabo; Li, Fa-Sheng; Li, Jian-Rong

    2014-11-28

    Metal-organic frameworks (MOFs) have great potential for applications in chromatography due to their highly tailorable porous structures and unique properties. In this work, the stable MOF UiO-66 was evaluated as both a normal-phase (NP-) and a reverse-phase (RP-) stationary phase in the high performance liquid chromatography (HPLC) to separate substituted benzenes (SBs) and polycyclic aromatic hydrocarbons (PAHs). It was found that the mobile phase composition has a significant effect on the HPLC separation. Baseline RP-HPLC separations of xylene isomers; naphthalene and anthracene; naphthalene and chrysene; and naphthalene, fluorene, and chrysene were achieved using MeOH/H2O ratios of 80:20, 75:25, 85:15, and 75:25, respectively, on the UiO-66 column. Similarly, baseline NP-HPLC separations of xylene isomers and ethylbenzene; ethylbenzene, styrene, o-xylene, and m-xylene; and several PAHs were also obtained on the UiO-66 column with different mobile phase compositions. The relative standard deviations (RSDs) of retention time, peak height, peak area, and half peak width for five replicate separations of the tested analytes were within the ranges 0.2-0.4%, 0.2-1.6%, 0.7-3.9%, 0.4-1.1%, respectively. We also evaluated other critical HPLC parameters, including injected sample mass, column temperature, and the thermodynamic characters of both the RP-HPLC and the NP-HPLC separation processes. It was confirmed that the separation of SBs on a UiO-66 column was an exothermic process, controlled by both enthalpy change (ΔH) and entropy change (ΔS). The reverse shape selectivity, size selectivity, stacking effect, and electrostatic force played vital roles in the separations of these analytes. To the best of our knowledge, this method is one of the very few examples of using MOFs as the stationary phase in both NP-HPLC and RP-HPLC. MOF-based stationary phases may thus be applied in the separations and analyses of SBs and PAHs in environmental samples.

  18. Liquid chromatography-atmospheric pressure laser ionization-mass spectrometry (LC-APLI-MS) analysis of polycyclic aromatic hydrocarbons with 6-8 rings in the environment.

    PubMed

    Thiäner, Jan B; Achten, Christine

    2017-03-01

    A method has been developed for the sensitive and rapid analysis of polycyclic aromatic hydrocarbons (PAHs) in environmental samples using liquid chromatography time-of-flight mass spectrometry as well as the selective atmospheric pressure laser ionization (APLI) process (LC-APLI-MS). Upon analyzing 34 PAHs, the limits of detection of this method were found to range from 0.008 to 1.824 pg (0.024 pg for benzo[a]pyrene). The method therefore provides 30-fold to 5,400-fold increased sensitivity compared with the established GC-MS technique. This LC-APLI-MS method was optimized for higher molecular weight PAHs (C24-C30 PAHs with 6-8 rings), which are difficult to detect or cannot be detected by GC-MS. Using the LC-APLI-MS method, various 6- to 8-ring PAHs were detected in environmental samples for the first time. After developing the method, it was successfully validated in ruggedness tests. The concentrations determined by the LC-APLI-MS method were in good accord with the certified concentrations in three certified reference materials (contaminated soils and sediments). Upon applying the method to environmental samples, it was found that (1) the presence of dibenzo[a,i]pyrene and dibenzo[a,h]pyrene in urban soil samples could only be detected using LC-APLI-MS (i.e., not GC-MS) due to its high sensitivity, (2) a bituminous coal sample yielded 211 tentative peaks from aromatic compounds in the C24-C30 range, and (3) eleven of those compounds occurred in different environmental samples in similar patterns. Hence, 6- to 8-ring PAHs occur in solid environmental samples in which other 6-ring PAHs such as indeno[1,2,3-cd]pyrene or benzo[ghi]perylene may also be present. Some of these numerous higher molecular weight PAH compounds could have very high carcinogenic potential, which will need to be elucidated to ensure the reliability of PAH risk assessments.

  19. Deashing of coal liquids with ceramic membrane microfiltration and diafiltration. Final quarterly technical progress report, January 1, 1995--March 31, 1995

    SciTech Connect

    1995-12-01

    Removal of mineral matter from liquid hydrocarbons derived from the direct liquefaction of coal is required for product acceptability. Current methods include critical solvent de-ashing and filtration, both of which produce an ash reject stream containing up to 15% of the liquid hydrocarbon product. This program is directed towards development of an improved process for de-ashing and recovery of coal-derived residual oil: the use of ceramic membranes for high-temperature microfiltration and diafiltration. Using laboratory-scale ceramic membrane modules, samples of a coal-derived residual oil containing ash will be processed by crossflow microfiltration, followed by solvent addition and refiltration (diafiltration). Recovery of de-ashed residual oil will be demonstrated. Data from this program will be used to develop a preliminary engineering design and cost estimate for a demonstration pilot plant incorporating full-scale membrane modules. In addition, estimates for production system capital and operating costs will be developed to assess process economic feasibility. The five program tasks include (1) ceramic membrane fabrication, (2) membrane test system assembly, (3) testing of the ceramic membranes, (4) design of a demonstration system using full scale membrane modules, and (5) development of estimates for microfiltration capital and operating costs and assessment of process economic feasibility.

  20. Final report-passive safety optimization in liquid sodium-cooled reactors.

    SciTech Connect

    Cahalana, J. E.; Hahn, D.; Nuclear Engineering Division; Korea Atomic Energy Research Inst.

    2007-08-13

    This report summarizes the results of a three-year collaboration between Argonne National Laboratory (ANL) and the Korea Atomic Energy Research Institute (KAERI) to identify and quantify the performance of innovative design features in metallic-fueled, sodium-cooled fast reactor designs. The objective of the work was to establish the reliability and safety margin enhancements provided by design innovations offering significant potential for construction, maintenance, and operating cost reductions. The project goal was accomplished with a combination of advanced model development (Task 1), analysis of innovative design and safety features (Tasks 2 and 3), and planning of key safety experiments (Task 4). Task 1--Computational Methods for Analysis of Passive Safety Design Features: An advanced three-dimensional subassembly thermal-hydraulic model was developed jointly and implemented in ANL and KAERI computer codes. The objective of the model development effort was to provide a high-accuracy capability to predict fuel, cladding, coolant, and structural temperatures in reactor fuel subassemblies, and thereby reduce the uncertainties associated with lower fidelity models previously used for safety and design analysis. The project included model formulation, implementation, and verification by application to available reactor tests performed at EBR-II. Task 2--Comparative Analysis and Evaluation of Innovative Design Features: Integrated safety assessments of innovative liquid metal reactor designs were performed to quantify the performance of inherent safety features. The objective of the analysis effort was to identify the potential safety margin enhancements possible in a sodium-cooled, metal-fueled reactor design by use of passive safety mechanisms to mitigate low-probability accident consequences. The project included baseline analyses using state-of-the-art computational models and advanced analyses using the new model developed in Task 1. Task 3--Safety

  1. Production of liquid fuels and chemicals by microalgae. Final subcontract report

    SciTech Connect

    Weissman, J.C.; Goebel, R.P.

    1985-03-01

    An overall objective of the project was to conceptually determine if simple open pond systems have application for the production of fuels from microalgae. To demonstrate the overall objective, work concentrated on showing the potential microalgal yields that are possible from an open pond system on a sustained basis. Furthermore, problems associated with this experimental system were documented and reported so that future endeavors shall benefit. Finally, operational costs were documented to permit preliminary economic analysis of the system. The major conclusions of this project can be summarized as follows: (1) Using two wildtype species in northern California a yearly average productivity of 15 gm/m/sup 2//day, or 24 tons/acre/yr can be obtained in water with TDS = 4 to 8 ppt. (2) This can probably be increased to 20 to 25 gm/m/sup 2//day or 32 to 40 tons/acre/y in southern California. (3) Productivity can probably be further increased by using competitive strains screened for low respiration rates, tolerances to high levels of dissolved oxygen, broad temperature optima, and resistance to photoinhibition. (4) In systems with randomized, turbulent mixing, productivity is independent of channel velocity at least for productivities up to 25 to 30 gm/m/sup 2//day and velocities from 1 to 30 cm/sec. (5) Storage product induction requires one to three days of growth in batch mode under n-depleted conditions. (6) Critical cost centers include CO/sub 2/ input, harvesting and system capital cost. (7) Media recycling, necessary for water conservation, has no adverse effects, at least in the short term for strains which do not excrete organics, and when the harvesting method is at least moderately effective for all algal forms which may be present. 8 refs., 28 figs., 56 tabs.

  2. Final report on regional supplementary comparison SIM.M.FF-S5: Volume of liquids at 50 mL

    NASA Astrophysics Data System (ADS)

    Morales, Abed; Malta, Dalni; Kornblit, Fernando; Ramírez, Ruben R.; Arias, Roberto; Trujillo, Sonia

    2012-01-01

    A regional supplementary comparison for the volume of liquid at 50 mL was conducted during October 2009 to June 2010 between the SIM members CENAM, INTI, INMETRO, INDECOPI and INTN. The transfer standard consisted of two 50 mL glass pycnometers, of the Gay Lussac type. CENAM acted as the pilot, collected the measurement results, analyzed the data and produced the comparison report. The median of all participants' results was used to calculate the regional comparison reference value because the result for one of the two pycnometers in one laboratory failed the chi-squared test at the 0.05 probability level. The measurements reported by the participants show an excellent overlap in four out of the five NMIs (-34×10-6 < Di < 29×10-6). The degree of equivalence obtained herein will be taken into account for the preparation of calibration and measurement capabilities claims from the participants. Main text. To reach the main text of this paper, click on Final Report. Note that this text is that which appears in Appendix B of the BIPM key comparison database kcdb.bipm.org/. The final report has been peer-reviewed and approved for publication by the SIM, according to the provisions of the CIPM Mutual Recognition Arrangement (CIPM MRA).

  3. Part A: Hydrocarbon Suspension in Slush Hydrogen

    NASA Technical Reports Server (NTRS)

    Sindt, C. F.

    1972-01-01

    Methods of preparing suspensions of a hydrocarbon in slush hydrogen for nuclear fuel element corrosion inhibition in rocket engines were investigated. Suspensions were prepared using approximately 5000 ppm by mass of methane, ethane, or cyclopropane in slush hydrogen. The suspensions were stable in the slush, but the hydrocarbons settled out of the liquid melt.

  4. Utilization of an ionic liquid in situ preconcentration method for the determination of the 15 + 1 European Union polycyclic aromatic hydrocarbons in drinking water and fruit-tea infusions.

    PubMed

    Germán-Hernández, Mónica; Crespo-Llabrés, Pilar; Pino, Verónica; Ayala, Juan H; Afonso, Ana M

    2013-08-01

    An ionic liquid (IL) in situ preconcentration method was optimized and applied to the monitoring of the 15 + 1 European Union polycyclic aromatic hydrocarbons in water and fruit-tea infusions. The optimized method utilizes 10 mL of water (or infusion) containing 38 μL of the IL 1-butyl-3-methylimidazolium chloride and a content of 36.1 g/L NaCl, which are mixed with Li-NTf2 (340 μL, 0.2 g/mL), followed by vortex (4 min) and centrifugation (5 min). The obtained microdroplet containing hydrocarbons is diluted with acetonitrile and injected into an HPLC with UV/Vis and fluorescence detection. The method presented average enrichment factors of 127 for water (tap water and bottled water) and 27 for two fruit-tea infusions; with average relative recoveries of 86.7 and 106% for water and fruit-tea infusions, respectively. The method was sensitive, with detection limits ranging from 0.001 to 0.050 ng/mL in water, and from 0.010 to 0.600 ng/mL in fruit-tea infusions, for the fluorescent hydrocarbons. Real extraction efficiencies ranged from 12.7 to 58.7% for water, and from 20.2 to 117% for the infusions. The method was also fast (~12 min) and free of organic solvents in the extraction step.

  5. Mercury-free PVT apparatus for thermophysical property analyses of hydrocarbon reservoir fluids. Final report, August 16, 1990--July 31, 1992

    SciTech Connect

    Lansangan, R.M.; Lievois, J.S.

    1992-08-31

    Typical reservoir fluid analyses of complex, multicomponent hydrocarbon mixtures include the volumetric properties, isothermal compressibility, thermal expansivity, equilibrium ratios, saturation pressure, viscosities, etc. These parameters are collectively referred to as PVT properties, an acronym for the primary state variables; pressure, volume, and temperature. The reservoir engineer incorporates this information together with the porous media description in performing material balance calculations. These calculations lead to the determination (estimation) of the initial hydrocarbon in-place, the future reservoir performance, the optimal production scheme, and the ultimate hydrocarbon recovery. About four years ago, Ruska Instrument Corporation embarked on a project to develop an apparatus designed to measure PVT properties that operates free of mercury. The result of this endeavor is the 2370 Hg-Free PVT system which has been in the market for the last three years. The 2370 has evolved from the prototype unit to its present configuration which is described briefly in this report. The 2370 system, although developed as a system-engineered apparatus based on existing technology, has not been exempt from this burden-of-proof Namely, the performance of the apparatus under routine test conditions with real reservoir fluids. This report summarizes the results of the performance and applications testing of the 2370 Hg-Free PVT system. Density measurements were conducted on a pure fluid. The results were compared against literature values and the prediction of an equation of state. Routine reservoir fluid analyses were conducted with a black oil and a retrograde condensate gas mixtures. Limited comparison of the results were performed based on the same tests performed on a conventional mercury-based PVT apparatus. The results of these tests are included in this report.

  6. Optimization of the OPLS-AA Force Field for Long Hydrocarbons.

    PubMed

    Siu, Shirley W I; Pluhackova, Kristyna; Böckmann, Rainer A

    2012-04-10

    The all-atom optimized potentials for liquid simulations (OPLS-AA) force field is a popular force field for simulating biomolecules. However, the current OPLS parameters for hydrocarbons developed using short alkanes cannot reproduce the liquid properties of long alkanes in molecular dynamics simulations. Therefore, the extension of OPLS-AA to (phospho)lipid molecules required for the study of biological membranes was hampered in the past. Here, we optimized the OPLS-AA force field for both short and long hydrocarbons. Following the framework of the OPLS-AA parametrization, we refined the torsional parameters for hydrocarbons by fitting to the gas-phase ab initio energy profiles calculated at the accurate MP2/aug-cc-pVTZ theory level. Additionally, the depth of the Lennard-Jones potential for methylene hydrogen atoms was adjusted to reproduce the densities and the heats of vaporization of alkanes and alkenes of different lengths. Optimization of partial charges finally allowed to reproduce the gel-to-liquid-phase transition temperature for pentadecane and solvation free energies. It is shown that the optimized parameter set (L-OPLS) yields improved hydrocarbon diffusion coefficients, viscosities, and gauche-trans ratios. Moreover, its applicability for lipid bilayer simulations is shown for a GMO bilayer in its liquid-crystalline phase.

  7. 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.

  8. Evaluation of solidification/stabilization for treatment of a petroleum hydrocarbon contaminated sludge from Fort Polk Army Installation, Louisiana. Final report

    SciTech Connect

    Channell, M.G.; Preston, K.T.

    1996-09-01

    In the course of normal operations and training, soldiers and civilian personnel operate many Army vehicles on a day-today basis. These vehicles must be cleaned before they can be returned to the motor pool area of an Army base. The cleaning of these vehicles bas posed a problem with the operation and maintenance of oil/water separators located at vehicle washrack facilities. An oily sludge forms in the oil/water separator and is hard to handle and cannot be disposed of in an ordinary manner. This study used solidification/stabilization to treat the oily sludge found in the vehicle washrack oil/water separators. Solidification/stabilization is usually used to treat soils and sludges that contain heavy metals. Organic compounds, such as petroleum hydrocarbons found in the sludge, interfere with the setting of the solidification binding materials and thus produce a material that is not desirable for a treatment alternative. This study incorporates the use of dicalcium silicate as an additive to the solidification process to increase the strength and reduce the leachability of the petroleum hydrocarbons found in the sludge. This study shows that dicalcium silicate improves the handling characteristics of the sludge and reduces the leachability of the contaminants from the washrack sludge.

  9. Study of hydrocarbon miscible solvent slug injection process for improved recovery of heavy oil from Schrader Bluff Pool, Milne Point Unit, Alaska. Final report

    SciTech Connect

    1995-11-01

    The National Energy Strategy Plan (NES) has called for 900,000 barrels/day production of heavy oil in the mid-1990s to meet our national needs. To achieve this goal, it is important that the Alaskan heavy oil fields be brought to production. Alaska has more than 25 billion barrels of heavy oil deposits. Conoco, and now BP Exploration have been producing from Schrader Bluff Pool, which is part of the super heavy oil field known as West Sak Field. Schrader Bluff reservoir, located in the Milne Point Unit, North Slope of Alaska, is estimated to contain up to 1.5 billion barrels of (14 to 21{degrees}API) oil in place. The field is currently under production by primary depletion; however, the primary recovery will be much smaller than expected. Hence, waterflooding will be implemented earlier than anticipated. The eventual use of enhanced oil recovery (EOR) techniques, such as hydrocarbon miscible solvent slug injection process, is vital for recovery of additional oil from this reservoir. The purpose of this research project was to determine the nature of miscible solvent slug which would be commercially feasible, to evaluate the performance of the hydrocarbon miscible solvent slug process, and to assess the feasibility of this process for improved recovery of heavy oil from Schrader Bluff reservoir. The laboratory experimental work includes: slim tube displacement experiments and coreflood experiments. The components of solvent slug includes only those which are available on the North Slope of Alaska.

  10. Environmental Analysis of Endocrine Disrupting Effects from Hydrocarbon Contaminants in the Ecosystem - Final Report - 09/15/1996 - 09/14/2000

    SciTech Connect

    McLachlan, John A.

    2000-09-14

    The three major components of the research included: (a) a biotechnology based screening system to identify potential hormone mimics and antagonists (b) an animal screening system to identify biomarkers of endocrine effects and (c) a literature review to identify compounds at various DOE sites that are potential endocrine disruptors. Species of particular interest in this study were those that can serve as sentinel species (e.g., amphibians) and thus provide early warning signals for more widespread impacts on an ecosystem and its wildlife and human inhabitants. The objective of this basic research is to characterize the potential of common hydrocarbon contaminants in ecosystems to act as endocrine disruptors. Although the endocrine disrupting effects of contaminants such as dioxin and PCBs have been well characterized in both animals and humans, little is known about the capacities of other hydrocarbon contaminants to act as endocrine disruptors. Results obtained from this research project have provided information on endocrine disrupting contaminants for consideration in DOE's risk analyses for determining clean-up levels and priorities at contaminated DOE sites.

  11. 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.

  12. 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.

  13. Petroleum hydrocarbon-induced injury to subtidal marine sediment resources. Subtidal study number 1a. Exxon Valdez oil spill state/federal natural resource damage assessment final report

    SciTech Connect

    O`Clair, C.E.; Short, J.W.; Rice, S.D.

    1996-04-01

    To determine the distribution of oil in subtidal sediments after the Exxon Valdez oil spill we sampled sediments at six depths (0, 3, 6, 20, 40 and 100 m) at 53 locations in Prince William Sound and the northern Gulf of Alaska from 1989 to 1991. Results are based on 1278 sediment samples analyzed by gas chromatography/mass spectrometry. In 1989, the oil concentration was greatest in the Sound at 0 m. Outside the Sound, Exxon Valdez oil occurred at Chugach Bay, Hallo Bay, Katmai Bay, and Windy Bay in 1989. Hydrocarbons often matched Exxon Valdez oil less closely, oil was more patchily distributed, and the oil concentration decreased in sediments after 1989.

  14. Molecular bioanalytical methods for monitoring polynuclear aromatic hydrocarbon biodegradation in manufactured-gas-plant soils. Volume 2. Final report, September 1987-August 1991

    SciTech Connect

    King, J.M.H.; Sanseverino, J.; DiGrazia, P.M.; Applegate, B.M.; Sayler, G.S.

    1991-08-01

    The objectives of work described in the report were to provide fundamental information on the microbiology and biochemistry of polynuclear aromatic hydrocarbon (PAH) biodegradation, and to continue development and initiate applications for molecular techniques in providing needed information for biodegradation process monitoring and control. A significant portion of the effort was in support of research studies on dynamic systems analysis for PAH (presented in Volume I, GRI-91-0193). Specific work included: (1) Analyzing and developing a PAH degradative mixed bacterial culture for standardized bioreactor operation; (2) Developing a bacterial culture collection of organisms involved in PAH degradation; (3) Applying molecular techniques, principally DNA gene probe technology, for environmental diagnostic assessment of PAH bioremediation potential and biodegradation processes performance evaluation; (4) Development and application of reporter strain bioluminescent technology to improve capabilities of analysis for enzyme expression and/or bioavailability.

  15. Final design, fluid dynamic and structural mechanical analysis of a liquid hydrogen Moderator for the European Spallation Source

    NASA Astrophysics Data System (ADS)

    Bessler, Y.; Henkes, C.; Hanusch, F.; Schumacher, P.; Natour, G.; Butzek, M.; Klaus, M.; Lyngh, D.; Kickulies, M.

    2017-02-01

    The European Spallation Source (ESS) is currently in the construction phase and should have first beam on Target in 2019. ESS, located in Sweden, will be the most powerful spallation neutron source worldwide, with the goal to produce neutrons for research. As an in-kind partner the Forschungszentrum Juelich will among others, design and manufacture the four liquid hydrogen Moderators, which are located above and below the Target. Those vessels are confining the cold hydrogen used to reduce the energy level of the fast neutrons, produced by spallation in the Target, in order to make the neutrons usable for neutron scattering instruments. Due to the requirements [1], a fluid dynamic analysis with pressure and temperature depended hydrogen data, taking into account the pseudo critical phenomena and the pulsed neutronic heating (pressure waves) is necessary. With the fluid dynamic results, a structure mechanical analysis including radiation damage investigation (RCC-MRx code [5]), low temperature properties as well as strength reduction by welding can be realized. Finally, the manufacturing and welding completes the design process.

  16. Direct liquefaction Proof-of-Concept Program, Hydrocarbon Technologies, Inc., Lawrenceville, New Jersey. Final topical report, Bench Run 02 (227-91)

    SciTech Connect

    Comolli, A.G.; Pradhan, V.R.; Lee, T.L.K.; Karolkiewicz, W.F.; Popper, G.

    1996-09-01

    This report presents the results of Bench Run PB-02, conducted under the DOE Proof of Concept - Bench Option Program in direct coal liquefaction at Hydrocarbon Technologies, Inc. in Lawrenceville, New Jersey. Bench Run PB-02 was the second of the nine runs planned in the POC Bench Option Contract between the U.S. DOE and Hydrocarbon Technologies, Inc. The primary goal of this bench run was to evaluate the hybrid catalyst system, consisting of a dispersed slurry catalyst in one of the hydroconversion reactors and conventional supported extrudate catalyst in the other hydroconversion reactor, in a high-low two-stage temperature sequence, similar to the one operated at Wilsonville. This hybrid mode of operation with the high-low temperature sequence was studied during direct liquefaction of coal and in coprocessing of coal with Hondo resid and/or waste plastics under high space velocity operating conditions. Another important objective of Bench Run PB-02 was to investigate the novel {open_quotes}interstage internal recycle{close_quotes} of the second stage reactor slurry back to the first stage reactor. Other features of PB-02 included the use of an interstage separator and an in-line fixed bed hydrotreater. In general, it was found during Bench Run PB-02 that the {open_quote}hybrid type{close_quote} catalyst system was not effective for obtaining high levels of process performance as the {open_quote}all dispersed{close_quote} catalyst system, tested earlier, especially at high coal space velocities. The interstage internal recycle of second stage reactor slurry to the first stage reactor feed line was found to improve cracking of liquefaction products. The addition of small amounts of mixed plastics was found to improve the hydrogen utilization in both coal conversion and heavy oil hydrocracking reactions, i.e., plastics resulted in improving the overall distillate yield while at the same time reducing the light gas make and chemical hydrogen consumption.

  17. Pathways for Biomass-Derived Lignin to Hydrocarbon Fuels

    SciTech Connect

    Laskar, Dhrubojyoti; Yang, Bin; Wang, Huamin; Lee, Guo-Shuh J.

    2013-09-01

    Production of hydrocarbon fuel from biomass-derived lignin sources with current version of biorefinery infrastructure would significantly improve the total carbon use in biomass and make biomass conversion more economically viable. Thus, developing specialty and commodity products from biomass derived-lignin has been an important industrial and scientific endeavor for several decades. However, deconstruction of lignin’s complex polymeric framework into low molecular weight reactive moieties amenable for deoxygenation and subsequent processing into hydrocarbons has been proven challenging. This review offers a comprehensive outlook on the existing body of work that has been devoted to catalytic processing of lignin derivatives into hydrocarbon fuels, focusing on: (1) The intrinsic complexity and characteristic structural features of biomass-derived lignin; (2) Existing processing technologies for the isolation and depolymerization of bulk lignin (including detailed mechanistic considerations); (3) Approaches aimed at significantly improving the yields of depolymerized lignin species amenable to catalytic upgrading, and; (4) Catalytic upgrading, using aqueous phase processes for transforming depolymerized lignin to hydrocarbon derivatives. Technical barriers and challenges to the valorization of lignin are highlighted throughout. The central goal of this review is to present an array of strategies that have been reported to obtain lignin, deconstruct it to reactive intermediates, and reduce its substantial oxygen content to yield hydrocarbon liquids. In this regard, reaction networks with reference to studies of lignin model compounds are exclusively surveyed. Special attention is paid to catalytic hydrodeoxygenation, hydrogenolyis and hydrogenation. Finally, this review addresses important features of lignin that are vital to economic success of hydrocarbon production.

  18. Evaluation of sampling and analytical methods for nicotine and polynuclear aromatic hydrocarbon in indoor air. Final report, 1 February 1987-30 March 1987

    SciTech Connect

    Chuang, J.C.; Kuhlman, M.R.; Hannan, S.W.; Bridges, C.

    1987-11-01

    The objective of this project was to evaluate a potential collection medium, XAD-4 resin, for collecting nicotine and polynuclear aromatic hydrocarbon (PAH) and to determine whether one collection system and one analytical method will allow quantification of both compound classes in air. The extraction efficiency study was to determine the extraction method to quantitatively remove nicotine and PAH from XAD-4 resin. The results showed that a two-step Soxhlet extraction consisting of dichloromethane followed by ethyl acetate resulted in the best recoveries for both nicotine and PAH. In the sampling efficiency study, XAD-2 and XAD-4 resin were compared, in parallel, for collection of PAH and nicotine. Quartz fiber filters were placed upstream of both adsorbents to collect particles. Prior to sampling, both XAD-2 and XAD-4 traps were spiked with known amounts (2 microgram) of perdeuterated PAH and D3-nicotine. The experiments were performed with cigarette smoking and nonsmoking conditions. The spiked PAH were retained well in both adsorbents after exposure to more than 300 cu. m. of indoor air. The spiked XAD-4 resin gave higher recoveries for D3-nicotine than did the spiked XAD-2 resin. The collection efficiency for PAH for both adsorbents is very similar but higher levels of nicotine were collected on XAD-4 resin.

  19. Evaluation of interim and final waste forms for the newly generated liquid low-level waste flowsheet

    SciTech Connect

    Abotsi, G.M.K.; Bostick, D.T.; Beck, D.E.

    1996-05-01

    The purpose of this review is to evaluate the final forms that have been proposed for radioactive-containing solid wastes and to determine their application to the solid wastes that will result from the treatment of newly generated liquid low-level waste (NGLLLW) and Melton Valley Storage Tank (MVST) supernate at the Oak Ridge National Laboratory (ORNL). Since cesium and strontium are the predominant radionuclides in NGLLLW and MVST supernate, this review is focused on the stabilization and solidification of solid wastes containing these radionuclides in cement, glass, and polymeric materials-the principal waste forms that have been tested with these types of wastes. Several studies have shown that both cesium and strontium are leached by distilled water from solidified cement, although the leachabilities of cesium are generally higher than those of strontium under similar conditions. The situation is exacerbated by the presence of sulfates in the solution, as manifested by cracking of the grout. Additives such as bentonite, blast-furnace slag, fly ash, montmorillonite, pottery clay, silica, and zeolites generally decrease the cesium and strontium release rates. Longer cement curing times (>28 d) and high ionic strengths of the leachates, such as those that occur in seawater, also decrease the leach rates of these radionuclides. Lower cesium leach rates are observed from vitrified wastes than from grout waste forms. However, significant quantities of cesium are volatilized due to the elevated temperatures required to vitrify the waste. Hence, vitrification will generally require the use of cleanup systems for the off-gases to prevent their release into the atmosphere.

  20. Three-phase solid-liquid-vapor equilibria in the binary hydrocarbon systems methane-n-hexane and methane-benzene

    SciTech Connect

    Luks, K.; Hottovy, J.D.; Kohn, J.P.

    1981-10-01

    Pressure, temperature, liquid-phase compositions, and liquid-phase molar volumes are presented along the solid-liquid-vapor (SLV) loci of the binary systems methane-n-hexane and methane-benzene. The data were taken by using cryoscopic techniques and are compared to the solid-liquid (SL) data at elevated pressures of Kuebler and McKinley. The standard deviations of the smoothed SLV data for liquid-phase solute composition presented herein from the raw SLV data are 3.7% for the methane-n-hexane system and 8.6% for the low-temperature branch of the methane-benzene system. The corresponding standard deviation for the high-temperature (high solute composition) branch for the system methane-benzene is less than 0.7%. 8 refs.

  1. Rapid quick, easy, cheap, effective, rugged, and safe extraction with novel phospholipid cleanup: A streamlined ultra high performance liquid chromatography with ultraviolet detection approach for screening polycyclic aromatic hydrocarbons in avian blood cells and plasma.

    PubMed

    Provatas, Anthony A; Yevdokimov, Alexander V; King, Cory A; Gatley, Emma L; Stuart, James D; Evers, David C; Perkins, Christopher R

    2015-08-01

    A streamlined method has been developed for the isolation and analysis of polycyclic aromatic hydrocarbons in avian blood cells and plasma utilizing quick, easy, cheap, effective, rugged, and safe extraction in combination with novel phospholipid cleanup technology. A variety of traditional extraction and cleanup techniques have been employed in the preparation and analysis of polycyclic aromatic hydrocarbonsin a variety of matrices; liquid-liquid partitioning, solid-phase extractions, gel permeation chromatography, and column chromatography are all effective techniques, however they are laborious and time consuming processes that require large amounts of solvent. Using quick, easy, cheap, effective, rugged, and safe extraction coupled with phospholipid cleanup, samples can be quickly screened while maintaining high throughput and sensitivity. With a liquid chromatography approach, analysis times may be kept short at 16 min while maintaining high analyte recovery. Recoveries in quality control samples ranged from 70 to 109%, with average surrogate recoveries of 80.6 ± 1.10%. The result of using a quick, easy, cheap, effective, rugged, and safe extraction approach in conjunction with phospholipid cleanup is a methodology that significantly reduces sample preparation time and solvent use while maintaining high sensitivity and reproducibility.

  2. Design and economics of a lignite-to-SNG (substitute natural gas) facility using Lurgi gasifiers for lignite gasification and the Texaco Partial Oxidation Process to gasify Lurgi by-product liquids. Final topical report, April 1985-November 1985

    SciTech Connect

    Smith, J.T.; Smelser, S.C.

    1985-01-01

    A design and cost estimate was prepared for a 250 billion Btu/day lignite-to-SNG plant that uses Lurgi dry-bottom gasifiers to gasify lignite and the Texaco Partial Oxidation (POX) process to gasify the various hydrocarbon liquids produced by the Lurgi process. Also presented are plant performance and economic comparisons between this plant design and a Base Case design prepared previously in which the Lurgi by-product liquids are burned in boilers and superheaters for steam production. The cost-of-gas for the Study Case is approximately 1.5% higher than the cost-of-gas for the Base Case. It is slightly more economical to burn Lurgi liquids than to gasify them in an auxiliary unit, primarily because if liquids are gasified, additional coal-fired boilers are required for generation of process steam and these are substantially more expensive than boilers fired with liquid fuel.

  3. Mesoporous titanium oxide with high-specific surface area as a coating for in-tube solid-phase microextraction combined with high-performance liquid chromatography for the analysis of polycyclic aromatic hydrocarbons.

    PubMed

    Wang, Xiuqin; Feng, Juanjuan; Bu, Yanan; Tian, Yu; Luo, Chuannan; Sun, Min

    2017-06-01

    Stainless-steel wires coated with mesoporous titanium oxide were placed into a polyether ether ketone tube for in-tube solid-phase microextraction, and the coating sorbent was characterized by X-ray diffraction and scanning electron microscopy. It was combined with high-performance liquid chromatography to build an online system. Using eight polycyclic aromatic hydrocarbons as the analytes, some conditions including sample flow rate, sample volume, organic solvent content, and desorption time were investigated. Under optimum conditions, an online analysis method was established and provided good linearity (0.03-30 μg/L), low detection limits (0.01-0.10 μg/L), and high enrichment factors (77.6-678). The method was applied to determine target analytes in river water and water sample of coal ash, and the recoveries are in the range of 80.6-106.6 and 80.9-103.5%, respectively. Compared with estrogens and plasticizers, extraction coating shows better extraction efficiency for polycyclic aromatic hydrocarbons. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  4. Ultra performance liquid chromatography-atmospheric pressure photoionization-tandem mass spectrometry for high-sensitivity and high-throughput analysis of U.S. Environmental Protection Agency 16 priority pollutants polynuclear aromatic hydrocarbons.

    PubMed

    Cai, Sheng-Suan; Syage, Jack A; Hanold, Karl A; Balogh, Michael P

    2009-03-15

    In this work, we demonstrate the utility of ultra performance liquid chromatography-atmospheric pressure photoionization-tandem mass spectrometry (UPLC-APPI-MS/MS) for high-sensitivity and high-throughput analysis of United States Environmental Protection Agency (U.S. EPA) 16 priority pollutants polycyclic aromatic hydrocarbons (PAHs). Analyses were performed on a Waters Acquity-TQD equipped with Syagen's PhotoMate APPI source. All 16 PAHs were analyzed on column in approximately 3.5 min with excellent chromatographic separation for all PAH isomers and with low picogram detection limits on column for all analytes using chlorobenzene as a dopant. Dynamic linear ranges were evaluated and found to cover at least 3-4 orders of magnitude. In comparison with the existing U.S. EPA methods, this approach improves instrument sample throughput by at least 10-fold.

  5. Hydrocarbon exposure, pancreatitis, and bile acids.

    PubMed Central

    Hotz, P; Pilliod, J; Bourgeois, R; Boillat, M A

    1990-01-01

    The data on hydrocarbon induced pancreatitis are conflicting. This question was therefore studied in a non-selected population exposed to hydrocarbons and in "formerly" exposed workers. Neither the past clinical history nor the pancreatic tests provided any evidence for a causal relation between exposure and pancreatitis. No signs of hydrocarbon induced liver damage were seen either. As a healthy worker effect cannot be totally excluded, however, a case-control study in a group of patients suffering from non-alcohol induced pancreatitis could give useful indications for finally excluding the possibility of pancreatitis being induced by hydrocarbons. PMID:2271391

  6. Evaluation of mineral oil saturated hydrocarbons (MOSH) and mineral oil aromatic hydrocarbons (MOAH) in pure mineral hydrocarbon-based cosmetics and cosmetic raw materials using (1)H NMR spectroscopy.

    PubMed

    Lachenmeier, Dirk W; Mildau, Gerd; Rullmann, Anke; Marx, Gerhard; Walch, Stephan G; Hartwig, Andrea; Kuballa, Thomas

    2017-01-01

    Mineral hydrocarbons consist of two fractions, mineral oil saturated hydrocarbons (MOSH) and mineral oil aromatic hydrocarbons (MOAH). MOAH is a potential public health hazard because it may include carcinogenic polycyclic compounds. In the present study, 400 MHz nuclear magnetic resonance (NMR) spectroscopy was introduced, in the context of official controls, to measure MOSH and MOAH in raw materials or pure mineral hydrocarbon final products (cosmetics and medicinal products). Quantitative determination (qNMR) has been established using the ERETIC methodology (electronic reference to access in vivo concentrations) based on the PULCON principle (pulse length based concentration determination). Various mineral hydrocarbons (e.g., white oils, paraffins or petroleum jelly) were dissolved in deuterated chloroform. The ERETIC factor was established using a quantification reference sample containing ethylbenzene and tetrachloronitrobenzene. The following spectral regions were integrated: MOSH δ 3.0 - 0.2 ppm and MOAH δ 9.2 - 6.5, excluding solvent signals. Validation showed a sufficient precision of the method with a coefficient of variation <6% and a limit of detection <0.1 g/100 g. The applicability of the method was proven by analysing 27 authentic samples with MOSH and MOAH contents in the range of 90-109 g/100 g and 0.02-1.10 g/100 g, respectively. It is important to distinguish this new NMR-approach from the hyphenated liquid chromatography-gas chromatography methodology previously used to characterize MOSH/MOAH amounts in cosmetic products. For mineral hydrocarbon raw materials or pure mineral hydrocarbon-based cosmetic products, NMR delivers higher specificity without any sample preparation besides dilution. Our sample survey shows that previous methods may have overestimated the MOAH amount in mineral oil products and opens new paths to characterize this fraction. Therefore, the developed method can be applied for routine monitoring of consumer products

  7. Evaluation of mineral oil saturated hydrocarbons (MOSH) and mineral oil aromatic hydrocarbons (MOAH) in pure mineral hydrocarbon-based cosmetics and cosmetic raw materials using 1H NMR spectroscopy

    PubMed Central

    Lachenmeier, Dirk W.; Mildau, Gerd; Rullmann, Anke; Marx, Gerhard; Walch, Stephan G.; Hartwig, Andrea; Kuballa, Thomas

    2017-01-01

    Mineral hydrocarbons consist of two fractions, mineral oil saturated hydrocarbons (MOSH) and mineral oil aromatic hydrocarbons (MOAH). MOAH is a potential public health hazard because it may include carcinogenic polycyclic compounds. In the present study, 400 MHz nuclear magnetic resonance (NMR) spectroscopy was introduced, in the context of official controls, to measure MOSH and MOAH in raw materials or pure mineral hydrocarbon final products (cosmetics and medicinal products). Quantitative determination (qNMR) has been established using the ERETIC methodology (electronic reference to access in vivo concentrations) based on the PULCON principle (pulse length based concentration determination). Various mineral hydrocarbons (e.g., white oils, paraffins or petroleum jelly) were dissolved in deuterated chloroform. The ERETIC factor was established using a quantification reference sample containing ethylbenzene and tetrachloronitrobenzene. The following spectral regions were integrated: MOSH δ 3.0 – 0.2 ppm and MOAH δ 9.2 - 6.5, excluding solvent signals. Validation showed a sufficient precision of the method with a coefficient of variation <6% and a limit of detection <0.1 g/100 g. The applicability of the method was proven by analysing 27 authentic samples with MOSH and MOAH contents in the range of 90-109 g/100 g and 0.02-1.10 g/100 g, respectively. It is important to distinguish this new NMR-approach from the hyphenated liquid chromatography-gas chromatography methodology previously used to characterize MOSH/MOAH amounts in cosmetic products. For mineral hydrocarbon raw materials or pure mineral hydrocarbon-based cosmetic products, NMR delivers higher specificity without any sample preparation besides dilution. Our sample survey shows that previous methods may have overestimated the MOAH amount in mineral oil products and opens new paths to characterize this fraction. Therefore, the developed method can be applied for routine monitoring of consumer products

  8. [Determination of chlorinated hydrocarbons in coffee beans].

    PubMed

    Wieczorek, Jolanta; Czyrska, Regina; Wieczorek, Zbigniew; Smoczyńska, Krystyna

    2002-01-01

    Chlorinated hydrocarbons (gamma-HCH, DDT and their analogous metabolites) were determined in coffee beans. Four sorts of green coffee beans and 18 sorts of burnt coffee beans were used in the research. The method was based on extraction of fat and its destruction with concentrated sulphuric acid. Chlorinated hydrocarbons were extracted with n-hexane, separated and quantitatively determined by gas chromatography. The presence of chlorinated hydrocarbons was detected in green coffee beans and, in smaller quantities, in burnt coffee beans. The concentration of chlorinated hydrocarbons was lower in medium and darkly burnt coffee beans than lightly burnt coffee. The level of DDT and its metabolites in final product decreased after coffee burning at higher temperatures. After brewing the grind coffee beans the remains of chlorinated hydrocarbons were detected in coffee-grounds at concentration to those found in coffee beans. Drinking of natural coffee does not influence an increase of intake the chlorinated hydrocarbons by human beings.

  9. Direct contact liquid-liquid heat exchanger for solar heated and cooled buildings. Final report, January 1, 1979-May 30, 1980

    SciTech Connect

    Karaki, S.; Brothers, P.

    1980-06-01

    The technical and economic feasibility of using a direct contact liquid-liquid heat exchanger (DCLLHE) storage unit in a solar heating and cooling system is established. Experimental performance data were obtained from the CSU Solar House I using a DCLLHE for both heating and cooling functions. A simulation model for the system was developed. The model was validated using the experimental data and applied in five different climatic regions of the country for a complete year. The life-cycle cost of the system was estimated for each application. The results are compared to a conventional solar system, using a standard shell-and-tube heat exchanger. It is concluded that while thare is a performance advantage with a DCLLHE system over a conventional solar system, the advantage is not sufficiently large to overcome slightly higher capital and operating costs for the DCLLHE system.

  10. Vapor-liquid phase behavior of the iodine-sulfur water-splitting process : LDRD final report for FY03.

    SciTech Connect

    Bradshaw, Robert W.; Larson, Richard S.; Lutz, Andrew E.

    2004-01-01

    This report summarizes the results of a one-year LDRD project that was undertaken to better understand the equilibrium behavior of the iodine-water-hydriodic acid system at elevated temperature and pressure. We attempted to extend the phase equilibrium database for this system in order to facilitate development of the iodine-sulfur water-splitting process to produce hydrogen to a commercial scale. The iodine-sulfur cycle for thermochemical splitting of water is recognized as the most efficient such process and is particularly well suited to coupling to a high-temperature source of process heat. This study intended to combine experimental measurements of vapor-liquid-liquid equilibrium and equation-of-state modeling of equilibrium solutions using Sandia's Chernkin software. Vapor-liquid equilibrium experiments were conducted to a limited extent. The Liquid Chernkin software that was developed as part of an earlier LDRD project was enhanced and applied to model the non-ideal behavior of the liquid phases.

  11. Liquid metal-wetted niobium fiber brushes and braid close clearance collectors in magnetic fields comparison. Final report

    SciTech Connect

    Sondergaard, N.; Reilly, P.; Dilling, V.

    1993-08-01

    Niobium fiber brushes wetted with liquid metals offer an alternative to the highly successful braid collector because of the inherent flexibility of the metal fibers. A slipring of niobium fiber brushes wetted with NaK78 was compared directly with an NaK braid collector in a model of a 300-kW homopolar generator. Collector tip velocities varied from zero to 67 m/sec, currents from zero to 4,000 A, and magnetic fields from zero to 1.2 T. Results indicate under all conditions the fiber brush collector was comparable or superior to the braid collector. Current collector, Rectangular channel, Liquid metal flows, Power losses.

  12. Energy efficient membrane processes for the separation of organic liquids: Part 1: Final report, September 28, 1982--December 31, 1986

    SciTech Connect

    Cabasso, I.; Acharya, H.R.; Korngold, E.; Liu, Z.; Stern, S.A.; Li, W.; Makenzie, T.; Poda, E.

    1987-10-01

    The potential usefulness of two membrane processes, namely, pervaporation and perstraction, for separating azeotropic mixtures of aromatic and aliphatic hydrocarbons was studied theoretically and experimentally. A third membrane process, osmotic phase-separation, was investigated experimentally. The separation of an azeotropic mixture of benzene and cyclohexane was used as an example. Part II of this report will discuss membrane processes for the separation of alcohol/water mixtures. Mathematical models of pervaporation and perstraction were developed for computer simulations of the processes. The perstraction model presented herein is the first of its kind. Additionally, the energy requirements and capital investments costs for the separation of an azeotropic benzene/cyclohexane mixture were determined and compared with those for extractive distillation. 31 refs., 64 figs., 19 tabs.

  13. Carbon neutral hydrocarbons.

    PubMed

    Zeman, Frank S; Keith, David W

    2008-11-13

    Reducing greenhouse gas emissions from the transportation sector may be the most difficult aspect of climate change mitigation. We suggest that carbon neutral hydrocarbons (CNHCs) offer an alternative pathway for deep emission cuts that complement the use of decarbonized energy carriers. Such fuels are synthesized from atmospheric carbon dioxide (CO2) and carbon neutral hydrogen. The result is a liquid fuel compatible with the existing transportation infrastructure and therefore capable of a gradual deployment with minimum supply disruption. Capturing the atmospheric CO2 can be accomplished using biomass or industrial methods referred to as air capture. The viability of biomass fuels is strongly dependent on the environmental impacts of biomass production. Strong constraints on land use may favour the use of air capture. We conclude that CNHCs may be a viable alternative to hydrogen or conventional biofuels and warrant a comparable level of research effort and support.

  14. Evolution of flow disturbances in cocurrent gas-liquid flows. Final report, November 1, 1993--October 31, 1994

    SciTech Connect

    McCready, M.J.

    1994-12-01

    Long-wave stability curves for two-layer laminar flow, laminar liquid and a turbulent gas (simulated with a polynomial profile) from the full differential equations and boundary conditions are compared to the standard 1-d equation methods of predicting flow regime transitions. The differential models predict instability at much less severe conditions than the integral equations -- as much as an order of magnitude when plotted on friction velocity -- liquid depth coordinates. Since this plot removes most of the base state`s effects, the 1-d models clearly are not predicting linear stability of anything. So agreement between the 1-d models with observed transitions is fortuitous since either the flow is too short or convenient parameter values have been chosen; otherwise flow regimes are not linked with linear stability. A polynomial profile gas, laminar liquid model, developed for a first approximation to turbulent flow, gives growth curves near the two-layer laminar exact solutions if the interfacial friction velocity and liquid depth are matched. The main differences are that the wavelength is predicted somewhat shorter for the turbulent model and the growth rate slightly larger for a laminar gas. These linear stability studies point to a need to determine the base state before significant results are obtained. Solutions for laminar flow in a rectangular channel over a solid wavy surface show that the wavelength/channel height ratio profoundly affects the stress variations. For waves long compared to channel height, pressure is completely in phase with wave slope, not wave height, as occurs for high Re in infinitely high channels. Nonlinear effects reduce the relative magnitude of the shear stress variation and phase angle that could explain saturation in the growth of waves formed by shear variation for very thin liquid layers. But since the pressure variation and phase are increased, this is not a likely explanation wave saturation on thicker layers.

  15. High temperature ceramic membrane reactors for coal liquid upgrading. Final report, September 21, 1989--November 20, 1992

    SciTech Connect

    Tsotsis, T.T.; Liu, P.K.T.; Webster, I.A.

    1992-12-31

    Membrane reactors are today finding extensive applications for gas and vapor phase catalytic reactions (see discussion in the introduction and recent reviews by Armor [92], Hsieh [93] and Tsotsis et al. [941]). There have not been any published reports, however, of their use in high pressure and temperature liquid-phase applications. The idea to apply membrane reactor technology to coal liquid upgrading has resulted from a series of experimental investigations by our group of petroleum and coal asphaltene transport through model membranes. Coal liquids contain polycyclic aromatic compounds, which not only present potential difficulties in upgrading, storage and coprocessing, but are also bioactive. Direct coal liquefaction is perceived today as a two-stage process, which involves a first stage of thermal (or catalytic) dissolution of coal, followed by a second stage, in which the resulting products of the first stage are catalytically upgraded. Even in the presence of hydrogen, the oil products of the second stage are thought to equilibrate with the heavier (asphaltenic and preasphaltenic) components found in the feedstream. The possibility exists for this smaller molecular fraction to recondense with the unreacted heavy components and form even heavier undesirable components like char and coke. One way to diminish these regressive reactions is to selectively remove these smaller molecular weight fractions once they are formed and prior to recondensation. This can, at least in principle, be accomplished through the use of high temperature membrane reactors, using ceramic membranes which are permselective for the desired products of the coal liquid upgrading process. An additional incentive to do so is in order to eliminate the further hydrogenation and hydrocracking of liquid products to undesirable light gases.

  16. Conversion of light hydrocarbon gases to metal carbides for production of liquid fuels and chemicals. Quarterly technical status report, January 1--March 31, 1993

    SciTech Connect

    Diaz, A.F.; Modestino, A.J.; Howard, J.B.; Peters, W.A.

    1993-04-01

    Work on this project will be performed according to two tasks: Task 1, Industrial Chemistry and Applied Kinetics of Light Hydrocarbon Gas Conversion to Metal Carbides H{sub 2} and CO. We are building a laboratory-scale electric are discharge reactor, in which to assess the technical feasibility of producing Mg{sub 2}C{sub 3}, H{sub 2}, and CO from methane and MgO. We will also do experimental runs with CaO as well as mixtures of CaO and MgO and measure conversions of methane, CaO and/or MgO, and yields of Mg{sub 2}C{sub 3}, and/or CaC{sub 2}, H{sub 2}, and CO to identify the operating conditions of interest for implementing these reactions on a commercial scale. Reaction conditions and parameters will be chosen based on the previous work at MIT with CaO and CH, and on results of thermodynamic and thermochemical kinetics calculations. Task 2: Mechanistic Foundations-For Convertings Light Hydrocarbon Gases to Metal Carbides-H{sub 2} and CO. We will evaluate the technical feasibility of carrying out methane reactions with CaO and MgO by thermal (e.g. 1500--2000{degrees}C) rather than under plasma conditions by performing experiments with the use of electrical screen heaters, heated tubular reactors, or other suitable apparatus. Extents and global rates of methane conversion, and yields as well as global production rates of CaC{sub 2}, Mg{sub 2}C{sub 3}, H{sub 2} and CO will be measured upon subjecting mixtures of methane and CaO and/or MgO to high temperatures and controlled residence times. We will conduct hypothesis-testing of possible mechanistic pathways with selected experiments and perform reaction modeling to better understand the underlying chemical and physical processes that could influence process scale-up possibilities.

  17. Liquid natural gas as a transportation fuel in the heavy trucking industry. Final technical report, May 10, 1994--December 30, 1995

    SciTech Connect

    Sutton, W.H.

    1995-12-31

    This report encompasses the first year of a proposed three year project with emphasis focused on LNG research issues in Use of Liquid Natural Gas as a Transportation Fuel in the Heavy Trucking Industry. These issues may be categorized as (i) direct diesel replacement with LNG fuel, and (ii) long term storage/utilization of LNG vent gases produced by tank storage and fueling/handling operation. Since this work was for fundamental research in a number of related areas to the use of LNG as a transportation fuel for long haul trucking, many of those results have appeared in numerous refereed journal and conference papers, and significant graduate training experiences (including at least one M.S. thesis and one Ph.D. dissertation) in the first year of this project. In addition, a potential new utilization of LNG fuel has been found, as a part of this work on the fundamental nature of adsorption of LNG vent gases in higher hydrocarbons; follow on research for this and other related applications and transfer of technology are proceeding at this time.

  18. Determination of saturated-hydrocarbon contamination in baby foods by using on-line liquid-gas chromatography and off-line liquid chromatography-comprehensive gas chromatography combined with mass spectrometry.

    PubMed

    Mondello, Luigi; Zoccali, Mariosimone; Purcaro, Giorgia; Franchina, Flavio Antonio; Sciarrone, Danilo; Moret, Sabrina; Conte, Lanfranco; Tranchida, Peter Quinto

    2012-10-12

    The present contribution describes an investigation directed towards the use of a rapid heart-cutting multidimensional LC-GC-FID method for the analysis of mineral oil saturated hydrocarbons (MOSH), contained in different types of homogenized solid baby food (fish, meat and fruit products). The fish and meat products all contained vegetable oil (sunflower), potentially an important source of mineral-oil contamination. Sixteen commercial baby food samples were subjected to analysis, with various degrees of MOSH contamination (from 0.3mg/kg to circa 14 mg/kg) found. Hence, MOSH contamination was found not only in the meat and fish products, but also in the fruit ones. A fruit-based baby food was lab-made, using the ingredients reported on the commercial product, and was found to be contaminated. The single ingredients were then subjected to LC-GC analysis, with corn starch and sugar found to be the source of contamination. For confirmation of the analytical findings, three of the sixteen samples were analyzed in two separate laboratories, using two distinct LC-GC methods, based on different interfaces. The results were confirmed, in qualitative terms, by collecting the LC fractions, relative to some of the food samples, and subjecting them to comprehensive two-dimensional GC-quadrupole mass spectrometry. Thus, mass spectral data were attained for the saturated hydrocarbons.

  19. Bioremediation of high molecular weight polyaromatic hydrocarbons co-contaminated with metals in liquid and soil slurries by metal tolerant PAHs degrading bacterial consortium.

    PubMed

    Thavamani, Palanisami; Megharaj, Mallavarapu; Naidu, Ravi

    2012-11-01

    Bioremediation of polyaromatic hydrocarbons (PAH) contaminated soils in the presence of heavy metals have proved to be difficult and often challenging due to the ability of toxic metals to inhibit PAH degradation by bacteria. In this study, a mixed bacterial culture designated as consortium-5 was isolated from a former manufactured gas plant (MGP) site. The ability of this consortium to utilise HMW PAHs such as pyrene and BaP as a sole carbon source in the presence of toxic metal Cd was demonstrated. Furthermore, this consortium has proven to be effective in degradation of HMW PAHs even from the real long term contaminated MGP soil. Thus, the results of this study demonstrate the great potential of this consortium for field scale bioremediation of PAHs in long term mix contaminated soils such as MGP sites. To our knowledge this is the first study to isolate and characterize metal tolerant HMW PAH degrading bacterial consortium which shows great potential in bioremediation of mixed contaminated soils such as MGP.

  20. Universal Route to Polycyclic Aromatic Hydrocarbon Analysis in Foodstuff: Two-Dimensional Heart-Cut Liquid Chromatography-Gas Chromatography-Mass Spectrometry.

    PubMed

    Nestola, Marco; Friedrich, Rainer; Bluhme, Patrick; Schmidt, Torsten C

    2015-06-16

    Analysis of polycyclic aromatic hydrocarbons (PAHs) in complex foodstuff is associated with complicated and work-intensive sample preparation. Chromatographic interference has to be faced in many situations. The scope of the current work was the development of a highly efficient two-dimensional heart-cut LC-LC-GC-MS method. Detection was performed with a time-of-flight mass spectrometer (TOF-MS) to allow for a comprehensive evaluation of the obtained data in terms of cleanup efficiency. Additionally, routine detection was performed with single quadrupole MS. An easy and quick generic sample preparation protocol was realized as a first step. During method development, focus was given to optimizing HPLC cleanup for complex foodstuff. Silica-, polymeric-, and carbon-based HPLC phases were tested. Coupling of silica gel to π-electron acceptor modified silica gel showed the best cleanup properties. A four rotary valve configuration allowed the usage of a single binary HPLC pump. Screening of several fatty and nonfatty food matrices showed the absence of unwanted matrix compounds in the cleaned-up PAH fraction down to the low picogram range using TOF-MS. Limits of quantitation (LOQ) were below 0.1 μg/kg for all EU priority PAHs. Recovery rates ranged from 82 to 111%. Validation data fully complied with EU Regulation 836/2011. Sample preparation was possible in 20 min. Interlacing of HPLC and GC allowed an average method runtime of 40 min per sample.

  1. Continuous thermodynamics and group contribution methods for coal liquids: Final report, October 1, 1986--October 1, 1989

    SciTech Connect

    Allen, D. T.; Behmanesh, N.; Vajdi, L. E.

    1989-01-01

    Structural profiles of narrow-boiling range fractions from three coal liquefaction processes were determined by identifying the major functional groups in the distillates and estimating their concentrations. The structural profiles were based on an extensive set of analytical data including results from elemental analysis, proton nuclear magnetic resonance, mass spectrometry, infrared spectroscopy and liquid chromatography. The functional group distributions were then interfaced with group contribution methods for property estimation. Heat capacities, critical constants, activity coefficients, hydrogen solubilities and vapor pressures were estimated for the narrow boiling fractions. The predictions have been compared to the predictions of more conventional property estimation methods and to experimental data. In addition, sensitivity analyses have been performed to determine which structural features in the coal derived liquids are most important in estimating the values of thermodynamic properties. 43 refs., 16 figs., 59 tabs.

  2. Methods of increasing hydrocarbon production from subterranean formations

    SciTech Connect

    Penny, G.S.; Gardner, T.R.

    1986-04-29

    A method is described of increasing the production of hydrocarbons from a hydrocarbon-containing subterranean carbonate-containing formation comprising introducing into the subterranean formation an anionic perfluoro substituted compound in a liquid carrier fluid whereby the compound is absorbed onto surfaces of the formation to reduce wetting of the surfaces by either hydrocarbons or water, the anionic perfluoro substituted compound being selected from individual compounds and mixtures thereof.

  3. Screening and determination of polycyclic aromatic hydrocarbons in seafoods using QuEChERS-based extraction and high-performance liquid chromatography with fluorescence detection.

    PubMed

    Gratz, Samuel R; Ciolino, Laura A; Mohrhaus, Angela S; Gamble, Bryan M; Gracie, Jill M; Jackson, David S; Roetting, John P; McCauley, Heather A; Heitkemper, Douglas T; Fricke, Fred L; Krol, Walter J; Arsenault, Terri L; White, Jason C; Flottmeyer, Michele M; Johnson, Yoko S

    2011-01-01

    A rapid, sensitive, and accurate method for the screening and determination of polycyclic aromatic hydrocarbons (PAHs) in edible seafood is described. The method uses quick, easy, cheap, effective, rugged, and safe (QuEChERS)-based extraction and HPLC with fluorescence detection (FLD). The method was developed and validated in response to the massive Deepwater Horizon oil spill in the Gulf of Mexico. Rapid and highly sensitive PAH screening methods are critical tools needed for oil spill response; they help to assess when seafood is safe for harvesting and consumption. Sample preparation involves SPE of edible seafood portions with acetonitrile, followed by the addition of salts to induce water partitioning. After centrifugation, a portion of the acetonitrile layer is filtered prior to analysis via HPLC-FLD. The chromatographic method uses a polymeric C18 stationary phase designed for PAH analysis with gradient elution, and it resolves 15 U.S. Environmental Protection Agency priority parent PAHs in fewer than 20 min. The procedure was validated in three laboratories for the parent PAHs using spike recovery experiments at PAH fortification levels ranging from 25 to 10 000 microg/kg in oysters, shrimp, crab, and finfish, with recoveries ranging from 78 to 99%. Additional validation was conducted for a series of alkylated homologs of naphthalene, dibenzothiophene, and phenanthrene, with recoveries ranging from 87 to 128%. Method accuracy was further assessed based on analysis of National Institute of Standards and Technology Standard Reference Material 1974b. The method provides method detection limits in the sub to low ppb (microg/kg) range, and practical LOQs in the low ppb (microg/kg) range for most of the PAH compounds studied.

  4. Determination of Polycyclic Aromatic Hydrocarbons in Commercial Parenteral Formulations and Medications Using High-Performance Liquid Chromatography with Diode Array Detection.

    PubMed

    Barichello, Marcia M; Bohrer, Denise; Viana, Carine; Carvalho, Leandro M; Nascimento, Paulo C

    2017-02-22

    HPLC coupled to UV diode array detection (DAD) is proposed for the determination of polycyclic aromatic hydrocarbons (PAHs) in pharmaceutical products for parenteral administration. Because rubber is a possible source of PAHs for these products, samples stored in containers with rubber parts were selected for the analysis. The basis for method optimization was EPA Method 8310, which determines 16 priority PAHs in ground water and wastewater by HPLC using both UV and fluorescence detection. Using DAD, two channels were selected for detection, with one operating at 254 nm for the detection of nine PAHs and the other at 225 nm for the detection of seven PAHs. This method allowed for the detection of PAHs using external calibration with LODs and LOQs ranging from 0.001 to 0.060 μg/mL and from 0.003 to 0.167 μg/mL, respectively. Within-day precision, expressed as RSD, varied from 1.24 to 7.76% for PAH concentrations from 0.05 to 0.50 μg/mL, and intraday precision varied from 3.10 to 9.40% for the same concentration range. Method accuracy was confirmed by recoveries of 75–120% of the spiked samples. This method was applied for the determination of PAHs in three commercial infusion solutions and in nine different medications stored in syringes prior to administration to patients. Twelve of 16 PAHs were found in these samples. Total PAH concentrations varied from 0.13 to 13.50 μg/mL. Pyrene was the most prevalent contaminant, being present in 11 of 12 samples in concentrations ranging from 0.17 to 4.80 μg/mL. This method presented good sensitivity for the measurement of PAH in the target samples, allowing for the determination of the 16 priority PAHs in one run and in 30 min.

  5. Final report on APMP key comparison of volume of liquids at 20 L and 100 mL: APMP.M.FF-K4

    NASA Astrophysics Data System (ADS)

    Man, John; Arias, Roberto; Terao, Yoshiya; Lee, Yong Jae; Ligong, Guo; Tulasombut, Verra; Chan, Tak Kin; Thai, Nguyen Hong; Steyn, Ronel; Sampath, H. L. I. S.

    2011-01-01

    This report presents the results of a key comparison of liquid volume measurement conducted between ten participating institutes during the period July 2006 to August 2008 within the framework of the Asia Pacifica Metrology Program (APMP). The transfer standards comprised one 20 L volume measure and two 100 mL glass pycnometers. These transfer standards had been used in a similar CIPM key comparison CCM.FF-K4 in 2003 to 2005. The pilot institute was the National Measurement Institute, Australia (NMIA), which together with CENAM act as link laboratories to the CCM.FF-K4 comparison. Main text. To reach the main text of this paper, click on Final Report. Note that this text is that which appears in Appendix B of the BIPM key comparison database kcdb.bipm.org/. The final report has been peer-reviewed and approved for publication by the CCM, according to the provisions of the CIPM Mutual Recognition Arrangement (MRA).

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

    DOEpatents

    Dumesic, James A [Verona, WI; Ruiz, Juan Carlos Serrano [Madison, WI; West, Ryan M [Madison, WI

    2012-04-03

    Described is a method to make liquid chemicals, such as functional intermediates, solvents, and liquid fuels from biomass-derived cellulose. The method is cascading; the product stream from an upstream reaction can be used as the feedstock in the next downstream reaction. The method includes the steps of deconstructing cellulose to yield a product mixture comprising levulinic acid and formic acid, converting the levulinic acid to .gamma.-valerolactone, and converting the .gamma.-valerolactone to pentanoic acid. Alternatively, the .gamma.-valerolactone can be converted to a mixture of n-butenes. The pentanoic acid so formed can be further reacted to yield a host of valuable products. For example, the pentanoic acid can be decarboxylated yield 1-butene or ketonized to yield 5-nonanone. The 5-nonanone can be hydrodeoxygenated to yield nonane, or 5-nonanone can be reduced to yield 5-nonanol. The 5-nonanol can be dehydrated to yield nonene, which can be dimerized to yield a mixture of C.sub.9 and C.sub.18 olefins, which can be hydrogenated to yield a mixture of alkanes. Alternatively, the nonene may be isomerized to yield a mixture of branched olefins, which can be hydrogenated to yield a mixture of branched alkanes. The mixture of n-butenes formed from .gamma.-valerolactone can also be subjected to isomerization and oligomerization to yield olefins in the gasoline, jet and Diesel fuel ranges.

  7. Air-water interface equilibrium partitioning coefficients of aromatic hydrocarbons

    NASA Astrophysics Data System (ADS)

    Cheng, Wen-Hsi; Chu, Fu-Sui; Liou, Jia-Jiunn

    The single equilibration technique was used to determine the equilibrium partitioning coefficients ( pc) of an air-water interface for target aromatic volatile organic compounds (VOCs), including benzene, toluene and ethylbenzene. The tested liquid concentrations ( CL) of VOC ranged from 0.5 to 20 mg/l, and the temperatures ( Tw) of the solutions were 300, 305, 310 and 315 K, respectively. The pc values were calculated using the gaseous concentrations ( Cg*) of aromatic hydrocarbons in equilibrium with the aqueous phase and the formula pc=( Cg*/ CL). The heats of VOC of liquid and gaseous phase transfer (Δ Htr) in pure water, and the highly linear regression relationship (with squared correlation coefficients, R2, from 0.900 to 0.999) between ( ln C g*) and (1/ Tw) are also evaluated. Experimental results indicated that the pc values of the target VOC components increase with Tw but, in contrast, are not significantly affected by CL in pure water. However, pc of more soluble compounds, like iso-propanol and methyl ethyl ketone, have been evaluated to be significant with CL in the earlier investigation. Finally, the co-solute effect on pc is also evaluated in this work, as determining pc of the aromatic hydrocarbons by using aqueous ethanol (in a volume ration of 1-15%) as solutes.

  8. 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.

  9. 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.

  10. 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.

  11. Determination of high-molecular weight polycyclic aromatic hydrocarbons in high performance liquid chromatography fractions of coal tar standard reference material 1597a via solid-phase nanoextraction and laser-excited time-resolved Shpol'skii spectroscopy.

    PubMed

    Wilson, Walter B; Alfarhani, Bassam; Moore, Anthony F T; Bisson, Cristina; Wise, Stephen A; Campiglia, Andres D

    2016-02-01

    This article presents an alternative approach for the analysis of high molecular weight - polycyclic aromatic hydrocarbons (HMW-PAHs) with molecular mass 302 Da in complex environmental samples. This is not a trivial task due to the large number of molecular mass 302 Da isomers with very similar chromatographic elution times and similar, possibly even virtually identical, mass fragmentation patterns. The method presented here is based on 4.2K laser-excited time-resolved Shpol'skii spectroscopy, a high resolution spectroscopic technique with the appropriate selectivity for the unambiguous determination of PAHs with the same molecular mass. The potential of this approach is demonstrated here with the analysis of a coal tar standard reference material (SRM) 1597a. Liquid chromatography fractions were submitted to the spectroscopic analysis of five targeted isomers, namely dibenzo[a,l]pyrene, dibenzo[a,e]pyrene, dibenzo[a,i]pyrene, naphtho[2,3-a]pyrene and dibenzo[a,h]pyrene. Prior to analyte determination, the liquid chromatographic fractions were pre-concentrated with gold nanoparticles. Complete analysis was possible with microliters of chromatographic fractions and organic solvents. The limits of detection varied from 0.05 (dibenzo[a,l]pyrene) to 0.24 µg L(-1) (dibenzo[a,e]pyrene). The excellent analytical figures of merit associated to its non-destructive nature, which provides ample opportunity for further analysis with other instrumental methods, makes this approach an attractive alternative for the determination of PAH isomers in complex environmental samples.

  12. Sorptive extraction using polydimethylsiloxane/metal-organic framework coated stir bars coupled with high performance liquid chromatography-fluorescence detection for the determination of polycyclic aromatic hydrocarbons in environmental water samples.

    PubMed

    Hu, Cong; He, Man; Chen, Beibei; Zhong, Cheng; Hu, Bin

    2014-08-22

    In this work, metal-organic frameworks (MOFs, Al-MIL-53-NH₂) were synthesized via the hydrothermal method, and novel polydimethylsiloxane/metal-organic framework (PDMS/MOFs, PDMS/Al-MIL-53-NH₂)-coated stir bars were prepared by the sol-gel technique. The preparation reproducibility of the PDMS/MOFs-coated stir bar was good, with relative standard deviations (RSDs) ranging from 4.8% to 14.9% (n=7) within one batch and from 6.2% to 16.9% (n=6) among different batches. Based on this fact, a new method of PDMS/MOFs-coated stir bar sorptive extraction (SBSE) and ultrasonic-assisted liquid desorption (UALD) coupled with high performance liquid chromatography-fluorescence detection (HPLC-FLD) was developed for the determination of polycyclic aromatic hydrocarbons (PAHs) in environmental water samples. To obtain the best extraction performance for PAHs, several parameters affecting SBSE, such as extraction time, stirring rate, and extraction temperature, were investigated. Under optimal experimental conditions, wide linear ranges and good RSDs (n=7) were obtained. With enrichment factors (EFs) of 16.1- to 88.9-fold (theoretical EF, 142-fold), the limits of detection (LODs, S/N=3) of the developed method for the target PAHs were found to be in the range of 0.05-2.94 ng/L. The developed method was successfully applied to the analysis of PAHs in Yangtze River and East Lake water samples. Copyright © 2014 Elsevier B.V. All rights reserved.

  13. The determination of occupational exposure to polycyclic aromatic hydrocarbons by the analysis of 1-hydroxypyrene in urine using a simple automated online column switching device and high-performance liquid chromatography.

    PubMed

    Hu, Jimmy; Hurst, James A; O'Donnell, Gregory E

    2012-06-01

    An analytical method using a liquid chromatograph combined with a simple online column switching sample pre-treatment system was developed for the determination of 1-hydroxypyrene (1-HP) in urine. This compound is the metabolite of pyrene and is used to assess the exposure of workers to polycyclic aromatic hydrocarbons (PAHs). After enzymatic hydrolysis, a urine sample was directly injected into a high-performance liquid chromatograph (HPLC) where it automatically underwent a sample cleanup using a column switching device. The procedure is simpler than previous methods because it uses only one switching valve, one extraction column and one HPLC pump. The analyte was retained on a short extraction column and after interferences were eluted to waste, was subsequently switched onto the analytical column. This allowed a short analysis time of 15 min. The calibration graph was found to be linear within the concentration range of 0.5 to 20 µg/L with a coefficient of determination exceeding r(2) = 0.99. Recoveries were found to be greater than 96% in the range 1 to 10 µg/L with intermediate precision of 2.5 to 5.8% relative standard deviation. This online method was verified by a comparison with an existing manual method by the analysis of 81 urine samples from workers exposed to PAHs and showed that the test results from both methods were in agreement with a probability obtained from the paired Student's t-test of P > 0.76. The proposed online method was found to be simple, fast and suited to routine analyses of 1-HP in urine for the assessment of occupational exposure to PAHs.

  14. Determination of high-molecular weight polycyclic aromatic hydrocarbons in high performance liquid chromatography fractions of coal tar standard reference material 1597a via solid-phase nanoextraction and laser-excited time-resolved Shpol'skii spectroscopy

    PubMed Central

    Wilson, Walter B.; Alfarhani, Bassam; Moore, Anthony F. T.; Bisson, Cristina; Wise, Stephen A.; Campiglia, Andres D.

    2016-01-01

    This article presents an alternative approach for the analysis of high molecular weight – polycyclic aromatic hydrocarbons (HMW-PAHs) with molecular mass 302 Da in complex environmental samples. This is not a trivial task due to the large number of molecular mass 302 Da isomers with very similar chromatographic elution times and similar, possibly even virtually identical, mass fragmentation patterns. The method presented here is based on 4.2 K laser-excited time-resolved Shpol'skii spectroscopy, a high resolution spectroscopic technique with the appropriate selectivity for the unambiguous determination of PAHs with the same molecular mass. The potential of this approach is demonstrated here with the analysis of a coal tar standard reference material (SRM) 1597a. Liquid chromatography fractions were submitted to the spectroscopic analysis of five targeted isomers, namely dibenzo[a,l]pyrene, dibenzo[a,e]pyrene, dibenzo[a,i]pyrene, naphtho[2,3-a]pyrene and dibenzo[a,h]pyrene. Prior to analyte determination, the liquid chromatographic fractions were pre-concentrated with gold nanoparticles. Complete analysis was possible with microliters of chromatographic fractions and organic solvents. The limits of detection varied from 0.05 (dibenzo[a,l]pyrene) to 0.24 μg L−1 (dibenzo[a,e]pyrene). The excellent analytical figures of merit associated to its non-destructive nature, which provides ample opportunity for further analysis with other instrumental methods, makes this approach an attractive alternative for the determination of PAH isomers in complex environmental samples. PMID:26653471

  15. Upgrading mild gasification liquids to produce electrode binder pitch. Final technical report, 1 September, 1992--31 August, 1993

    SciTech Connect

    Knight, R.A.

    1993-12-31

    The objective of this program is to investigate the production of electrode binder pitch, from mild gasification liquids. The IGT MILDGAS process pyrolyzes coal in a fluidized/entrained bed to produce solid, gas, and liquid co-products. The largest market for pitch made from coal liquids is the aluminum industry, which uses it to make carbon anodes for electrolytic furnaces. In this project, crude pitch from the DOE-sponsored MILDGAS process research programs being modified by a flash thermocracking technique to achieve specifications typical of a binder pitch. Atomization of the pitch at the thermocracker inlet is being examined as a method of optimizing the particle size of polymerized pitch components. Six successful thermocracking tests were performed with a crude Illinois No. 6 pitch from 1,110 F MILDGAS PRU runs. The tests were conducted at 1,200--1,500 F with pitch feed rates of 2.6--12.7 g/min and residence times of 2.6--4.5 seconds. Tests were conducted with and without an atomizing nozzle to evaluate the effects of atomization on the primary quinoline- and toluene-insoluble (QI and TI) content of the pitch. Key pitch properties improved in all cases, with higher temperatures resulting in increased softening point (187--273 F), QI (10--16%), TI (18--41%), coking value (38--55%), C:H ratio (1.17--1.57), and density (1.16--1.26). Higher reactor loading appears to promote more coke and gas production, but atomization promotes higher yield of cracked pitch, oil, and gas and less coke. The products of pitch cracking ranged from 26--54 wt% cracked pitch, 13--44 wt% coke, 16--28 wt% oils, and 3--23 wt% high-Btu gas. The pitch cokes had C:H atomic ratios of 1.95--2.93, which could be increased by calcination for use as a carbon anode filler.

  16. Ecological risk assessment report, submerged quench incinerator, task IRA-2, basin F liquids treatment design. Version 3. 0. Final report

    SciTech Connect

    Not Available

    1991-03-01

    The objective of this ecological risk assessment is to evaluate the potential impacts of on-site incineration of Basin F liquids. Twenty-nine chemicals were evaluated for potential adverse effects to terrestrial and aquatic wildlife and vegetation on RMA. Based on this assessment, it is concluded that the operation of the submerged quench incinerator poses no quantifiable risks to the wildlife and vegetation. The assessment is divided into the following sections: description of the area - terrestrial and aquatic ecology; contaminants of concern; ecological exposure - description of contaminant transport from incinerator to environment; ecological risk - development of risk criteria, risk characterization; assumptions and uncertainties.

  17. Improved liquid/solids handling module. Final report 2321:01, 1 September 1979-31 October 1980

    SciTech Connect

    West, L.K.

    1980-01-01

    A Mobile Liquid/Solids handling (L/S) unit was constructed that is the active element for a low cost Advanced Primary Geothermal Heat Exchanger (APEX), presently under development. The L/S system incorporates two alternating hydrocyclone-accumulator tank combinations and an injection pump. Sand particles are injected into the main flow and then separated and recirculated at capture efficiencies of greater than 99%. The system was tested at varying flowrates, solids concentrations, and particle sizes to determine an optimum operating point.

  18. Final Report for Fractionation and Separation of Polydisperse Nanoparticles into Distinct Monodisperse Fractions Using CO2 Expanded Liquids

    SciTech Connect

    Chistopher Roberts

    2007-08-31

    The overall objective of this project was to facilitate efficient fractionation and separation of polydisperse metal nanoparticle populations into distinct monodisperse fractions using the tunable solvent properties of gas expanded liquids. Specifically, the dispersibility of ligand-stabilized nanoparticles in an organic solution was controlled by altering the ligand-solvent interaction (solvation) by the addition of carbon dioxide (CO{sub 2}) gas as an antisolvent (thereby tailoring the bulk solvent strength) in a custom high pressure apparatus developed in our lab. This was accomplished by adjusting the CO{sub 2} pressure over the liquid dispersion, resulting in a simple means of tuning the nanoparticle precipitation by size. Overall, this work utilized the highly tunable solvent properties of organic/CO{sub 2} solvent mixtures to selectively size-separate dispersions of polydisperse nanoparticles (ranging from 1 to 20 nm in size) into monodisperse fractions ({+-}1nm). Specifically, three primary tasks were performed to meet the overall objective. Task 1 involved the investigation of the effects of various operating parameters (such as temperature, pressure, ligand length and ligand type) on the efficiency of separation and fractionation of Ag nanoparticles. In addition, a thermodynamic interaction energy model was developed to predict the dispersibility of different sized nanoparticles in the gas expanded liquids at various conditions. Task 2 involved the extension of the experimental procedures identified in task 1 to the separation of other metal particles used in catalysis such as Au as well as other materials such as semiconductor particles (e.g. CdSe). Task 3 involved using the optimal conditions identified in tasks 1 and 2 to scale up the process to handle sample sizes of greater than 1 g. An experimental system was designed to allow nanoparticles of increasingly smaller sizes to be precipitated sequentially in a vertical series of high pressure vessels by

  19. Analysis of polynuclear aromatic hydrocarbons in olive oil after solid-phase extraction using a dual-layer sorbent cartridge followed by high-performance liquid chromatography with fluorescence detection.

    PubMed

    Stenerson, Katherine K; Shimelis, Olga; Halpenny, Michael R; Espenschied, Ken; Ye, Maochun M

    2015-05-27

    A simple and easy direct solid-phase extraction (SPE) method was developed for the analysis of polynuclear aromatic hydrocarbons (PAHs) in olive oil using a dual-layer cartridge containing activated Florisil and a mixture of octadecyl (C18)-bonded and zirconia-coated silicas. Undiluted olive oil was applied directly to the SPE cartridge, and the sample was eluted with acetonitrile solvent. Background in the extract was found to be low enough for either gas chromatography-mass spectrometry (GC-MS) or high-performance liquid chromatography with fluorescence detection (HPLC-FLD) analysis. Average recoveries for 16 different PAHs from spiked olive oil replicates were >75%, with intraday precisions of <20% relative standard deviation (% RSD). Detection limits ranged from 0.2 to 1.0 μg/kg and, specifically for the PAHs listed in EC Regulation 835/2011, benzo(a)anthracene, chrysene, benzo(b)fluoranthene, and benzo(a)pyrene, were from 0.3 to 0.7 μg/kg. The method was then applied to determine the PAH content present in commercial samples of refined versus extra-virgin olive oils.

  20. Exploration of coordination polymer as sorbent for flow injection solid-phase extraction on-line coupled with high-performance liquid chromatography for determination of polycyclic aromatic hydrocarbons in environmental materials.

    PubMed

    Zhou, You-Ya; Yan, Xiu-Ping; Kim, Ki-Nam; Wang, Shan-Wei; Liu, Ming-Guang

    2006-05-26

    The copper(II) isonicotinate (Cu(4-C5H4N-COO)2(H2O)4) coordination polymer was prepared, characterized and explored as sorbent for flow injection solid-phase extraction on-line coupled with high-performance liquid chromatography (HPLC) for determination of trace polycyclic aromatic hydrocarbons (PAHs) in environmental matrices. Naphthalene, phenanthrene, anthracene, fluoranthene, benzo(b)fluoranthene, benzo(k)fluoranthene, benzo(a)pyrene and benzo(ghi)perylene with various shape, size and hydrophobicity were used as model analytes. The porosity of the coordination polymer allows these guest PAHs molecules to diffuse into the buck structure, and the shape and size of the pores lead to shape- and size-selectivity over the guests. The precolumn packed with the coordination polymer was shown to be promising for solid-phase extraction of PAHs in environmental samples with subsequent HPLC separation and UV detection. With extraction of 50 ml of sample solution, the enhancement factors for the PAHs studied ranged from 200 to 2337, depending on the shape, size and hydrophobic property of the PAHs. The detection limits (S/N = 3) of 2-14 ng l(-1) and the sample throughput of 3 samples h(-1) were obtained. The developed method was applied to the determination of trace PAHs in a certified reference material (coal fly ash) and local water samples.

  1. Simultaneous determination of thirteen polycyclic aromatic hydrocarbons and twelve aldehydes in cooked food by an automated on-line solid phase extraction ultra high performance liquid chromatography tandem mass spectrometry.

    PubMed

    Gosetti, Fabio; Chiuminatto, Ugo; Mazzucco, Eleonora; Robotti, Elisa; Calabrese, Giorgio; Gennaro, Maria Carla; Marengo, Emilio

    2011-09-16

    An on-line solid phase extraction (SPE) ultra high performance liquid chromatography tandem mass spectrometry method has been developed for the simultaneous identification and determination of thirteen polycyclic aromatic hydrocarbons (PAHs) and twelve aldehydes (derivatized with 2,4-dinitrophenylhydrazine). The chromatographic conditions have been optimized to obtain the maximum of sensitivity and resolution taking into account the different retention interactions and the different ionization conditions of PAHs and derivatized aldehydes. LOD values ranging from 0.028 to 0.768 μg L(-1) for PAHs and from 0.002 to 0.125 μg L(-1) for aldehydes were obtained. The resolution permitted the separation of four couples of PAH isomers. Sample pre-treatment and SPE were optimized in order to apply the whole methodology to the analysis of different food matrices as salmon, frankfurter, steak, and pork chop, subjected to different cooking modes (smoked, grilled, cooked in oil or in butter). Particular attention was devoted to the evaluation of matrix effect that was significantly reduced through the on-line SPE treatment. For each food matrix the method detection limits, the method quantitation limits, and the recovery R were evaluated. R was shown not to depend on analyte concentration in the explored concentration range (LOQ - 50.000 μg L(-1)): the average R percent ranges from 70.6% to 120.0%.

  2. Optimization of ultrasonic extraction and clean-up protocol for the determination of polycyclic aromatic hydrocarbons in marine sediments by high-performance liquid chromatography coupled with fluorescence detection

    NASA Astrophysics Data System (ADS)

    Peng, Xuewei; Yan, Guofang; Li, Xianguo; Guo, Xinyun; Zhou, Xiao; Wang, Yan

    2012-09-01

    The procedures of ultrasonic extraction and clean-up were optimized for the determination of polycyclic aromatic hydrocarbons (PAHs) in marine sediments. Samples were ultrasonically extracted, and the extracts were purified with a miniaturized silica gel chromatographic column and analyzed with high performance liquid chromatography (HPLC) with a fluorescence detector. Ultrasonication with methanol-dichloromethane (2:1, v/v) mixture gave higher extraction efficiency than that with dichloromethane. Among the three elution solvents used in clean-up step, dichloromethane-hexane (2:3, v/v) mixture was the most satisfactory. Under the optimized conditions, the recoveries in the range of 54.82% to 94.70% with RSDs of 3.02% to 23.22% for a spiked blank, and in the range of 61.20% to 127.08% with RSDs of 7.61% to 26.93% for a spiked matrix, were obtained for the 15 PAHs studied, while the recoveries for a NIST standard reference SRM 1941b were in the range of 50.79% to 83.78% with RSDs of 5.24% to 21.38%. The detection limits were between 0.75 ng L-1 and 10.99 ng L-1for different PAHs. A sample from the Jiaozhou Bay area was examined to test the established methods.

  3. Hydrocarbon mineralization potentials and microbial populations in marine sediments following the Exxon Valdez oil spill. Subtidal study number 1b. Exxon Valdez oil spill state/federal natural resource damage assessment final report

    SciTech Connect

    Braddock, J.F.; Rasley, B.T.; Yeager, T.R.; Lindstrom, J.E.; Brown, E.J.

    1992-06-01

    Following the Exxon Valdez oil spill in 1989, the authors measured numbers of hydrocarbon-degrading microoganisms and hydrocarbon mineralization potentials of microorganisms in oiled and unoiled surface sediments from the shore through 100 m depth offshore. The authors found both temporal and spatial variations in numbers and activity of hydrocarbon-degrading microorganisms with significant higher values at the oiled sites than at reference sites. The microbial data indicate mobilization between 1989 and 1990 of oil from the intertidal to surface sediments at 20, 40 and 100 m depths offshore.

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

    DOEpatents

    Dumesic, James A.; Ruiz, Juan Carlos Serrano; West, Ryan M.

    2015-06-30

    Described is a method to make liquid chemicals. The method includes deconstructing cellulose to yield a product mixture comprising levulinic acid and formic acid, converting the levulinic acid to .gamma.-valerolactone, and converting the .gamma.-valerolactone to pentanoic acid. Alternatively, the .gamma.-valerolactone can be converted to a mixture of n-butenes. The pentanoic acid can be decarboxylated yield 1-butene or ketonized to yield 5-nonanone. The 5-nonanone can be hydrodeoxygenated to yield nonane, or 5-nonanone can be reduced to yield 5-nonanol. The 5-nonanol can be dehydrated to yield nonene, which can be dimerized to yield a mixture of C.sub.9 and C.sub.18 olefins, which can be hydrogenated to yield a mixture of alkanes.

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

    DOEpatents

    Dumesic, James A [Verona, WI; Ruiz, Juan Carlos Serrano [Madison, WI; West, Ryan M [Madison, WI

    2014-01-07

    Described is a method to make liquid chemicals. The method includes deconstructing cellulose to yield a product mixture comprising levulinic acid and formic acid, converting the levulinic acid to .gamma.-valerolactone, and converting the .gamma.-valerolactone to pentanoic acid. Alternatively, the .gamma.-valerolactone can be conveted to a mixture of n-butenes. The pentanoic acid can be decarboxylated yield 1-butene or ketonized to yield 5-nonanone. The 5-nonanone can be hydrodeoxygenated to yield nonane, or 5-nonanone can be reduced to yield 5-nonanol. The 5-nonanol can be dehydrated to yield nonene, which can be dimerized to yield a mixture of C.sub.9 and C.sub.18 olefins, which can be hydrogenated to yield a mixture of alkanes.

  6. Upgrading mild gasification liquids to produce electrode binder pitch: Final technical report, September 1, 1993--October 31, 1994

    SciTech Connect

    Knight, R.A.

    1994-12-31

    The objective of this program is to investigate the production of electrode binder pitch, valued at $250--$300/ton, from mild gasification liquids. In the IGT MILDGAS process, the 400 C+ distillation residue (crude pitch) comprises up to 20 wt% of maf feed coal. The largest market for pitch made from coal liquids is the aluminum industry, which uses it to make carbon anodes for electrolytic furnaces. In this project, crude MILDGAS pitch is being modified by flash thermocracking to achieve binder pitch specifications. A 1-kg/h continuous unit has been built for operation up to 900 C at 2.5 atm, and parametric tests were conducted in N{sub 2}, H{sub 2} and 50% H{sub 2}/N{sub 2}. In general, thermocracking at 750--850 C in N{sub 2} resulted in a pitch which meets binder pitch requirements for QI, TI, softening point, and C:H ratio. Further improvements in density and sulfur content are required. Test anodes were prepared by Alcoa using the upgraded mild gasification pitch. All of the key anode properties (density, strength, resistivity, thermal properties, permeability, and reactivity) compared very favorably with those of electrodes made from a standard pitch binder.

  7. Analytical and experimental investigation of rubbing interaction in labyrinth seals for a liquid hydrogen fuel pump. Final report

    SciTech Connect

    Dolan, F.X.; Kennedy, F.E.; Schulson, E.M.

    1984-08-01

    Cracking of the titanium knife edges on the labyrinth seals of the liquid hydrogen fuel pump in the Space Shuttle main engine is considered. Finite element analysis of the thermal response of the knife edge in sliding contact with the wear ring surface shows that interfacial temperatures can be quite high and they are significantly influenced by the thermal conductivity of the surfaces in rubbing contact. Thermal shock experiments on a test specimen similar to the knife edge geometry demonstrate that cracking of the titanium alloy is possible in a situation involving repeated thermal cycles over a wide temperature range, as might be realized during a rub in the liquid hydrogen fuel pump. High-speed rub interaction tests were conducted using a representative knife edge and seal geometry over a broad range of interaction rates and alternate materials were experimentally evaluated. Plasma-sprayed aluminum-graphite was found to be significantly better than presently used aluminum alloy seals from the standpoint of rub performance. Ion nitriding the titanium alloy knife-edges also improved rub performance compared to the untreated baseline.

  8. "An Economic Process for Coal Liquefaction to Liquid Fuels" SBIR Phase II -- Final Scientific/Technical Report

    SciTech Connect

    Ganguli, Partha Sarathi

    2009-02-19

    The current commercial processes for direct coal liquefaction utilize expensive backmix-flow reactor system and conventional catalysts resulting in incomplete and retrogressive reactions that produce low distillate liquid yield and high gas yield, with high hydrogen consumption. The new process we have developed, which uses a less expensive reactor system and highly active special catalysts, resulted in high distillate liquid yield, low gas yield and low hydrogen consumption. The new reactor system using the special catalyst can be operated smoothly for direct catalytic coal liquefaction. Due to high hydrogenation and hydrocracking activities of the special catalysts, moderate temperatures and high residence time in each stage of the reactor system resulted in high distillate yield in the C4-650°F range with no 650°F+ product formed except for the remaining unconverted coal residue. The C4-650°F distillate is more valuable than the light petroleum crude. Since there is no 650°F+ liquid product, simple reforming and hydrotreating of the C4-650°F product will produce the commercial grade light liquid fuels. There is no need for further refinement using catalytic cracking process that is currently used in petroleum refining. The special catalysts prepared and used in the experimental runs had surface area between 40-155 m2/gm. The liquid distillate yield in the new process is >20 w% higher than that in the current commercial process. Coal conversion in the experimental runs was moderate, in the range of 88 - 94 w% maf-coal. Though coal conversion can be increased by adjustment in operating conditions, the purpose of limiting coal conversion to moderate amounts in the process was to use the remaining unconverted coal for hydrogen production by steam reforming. Hydrogen consumption was in the range of 4.0 - 6.0 w% maf-coal. A preliminary economic analysis of the new coal liquefaction process was

  9. Final report on EUROMET key comparison EUROMET.M.D-K2 (EUROMET 627) "Comparison of density determinations of liquid samples"

    NASA Astrophysics Data System (ADS)

    Bettin, Horst; Heinonen, Martti; Gosset, André; Zelenka, Zoltán; Lorefice, Salvatore; Hellerud, Kristen; Durlik, Hanna; Jordaan, Werner; Field, Ireen

    2016-01-01

    The results of the key comparison EUROMET 627 (EUROMET.M.D-K2) are presented. This project covered the density measurements of three liquids: dodecane, water and an oil of high viscosity measured at 15 °C, 20 °C and 40 °C. Seven European metrology laboratories and the South African laboratory CSIR-NML (now: NMISA) measured the densities at atmospheric pressure by hydrostatic weighing of solid density standards between 04 October 2001 and 18 December 2001. The stability and homogeneity of the liquids were investigated by the pilot laboratory PTB. The results generally show good agreement among the participants. Only for the simple Mohr-Westphal balances do the uncertainties seem to be underestimated by the laboratories. Furthermore, the measurement of high-viscosity oil was difficult for some laboratories. Nevertheless, the five laboratories PTB/DE, BNM/FR (now: LNE/FR), OMH/HU (now: MKEH/HU), IMGC/IT (now: INRIM/IT) and GUM/PL agree with each other for stated uncertainties of 0.05 kg/m3 or less. This satisfies the current needs of customers who wish to calibrate or check liquid density measuring instruments such as oscillation-type density meters. No reference values were calculated since the subsequent CCM key comparison CCM.D-K2 had a different scope and the EUROMET 627 comparison was soon superseded by the EURAMET 1019 (EURAMET.M.D-K2) comparison. To reach the main text of this paper, click on Final Report. Note that this text is that which appears in Appendix B of the BIPM key comparison database kcdb.bipm.org/. The final report has been peer-reviewed and approved for publication by the CCM, according to the provisions of the CIPM Mutual Recognition Arrangement (CIPM MRA).

  10. LIGHT NONAQUEOUS PHASE LIQUIDS

    EPA Science Inventory

    Nonaqueous phase liquids (NAPLS) are hydrocarbons that exist as a separate, immiscible phase when in contact with water and/or air. ifferences in the physical and chemical properties of water and NAPL result in the formation of a physical interface between the liquids which preve...

  11. LIGHT NONAQUEOUS PHASE LIQUIDS

    EPA Science Inventory

    Nonaqueous phase liquids (NAPLS) are hydrocarbons that exist as a separate, immiscible phase when in contact with water and/or air. ifferences in the physical and chemical properties of water and NAPL result in the formation of a physical interface between the liquids which preve...

  12. Hydrocarbon liquefaction: viability as a peak oil mitigation strategy.

    PubMed

    Höök, Mikael; Fantazzini, Dean; Angelantoni, André; Snowden, Simon

    2014-01-13

    Current world capacity of hydrocarbon liquefaction is around 400,000 barrels per day, providing a marginal share of the global liquid fuel supply. This study performs a broad review of technical, economic, environmental and supply chain issues related to coal-to-liquids (CTL) and gas-to-liquids (GTL). We find three issues predominate. First, significant amounts of coal and gas would be required to obtain anything more than a marginal production of liquids. Second, the economics of CTL plants are clearly prohibitive, but are better for GTL. Nevertheless, large-scale GTL plants still require very high upfront costs, and for three real-world GTL plants out of four, the final cost has been so far approximately three times that initially budgeted. Small-scale GTL holds potential for associated gas. Third, both CTL and GTL incur significant environmental impacts, ranging from increased greenhouse gas emissions (in the case of CTL) to water contamination. Environmental concerns may significantly affect growth of these projects until adequate solutions are found.

  13. Preapplication safety evaluation report for the Power Reactor Innovative Small Module (PRISM) liquid-metal reactor. Final report

    SciTech Connect

    Donoghue, J.E.; Donohew, J.N.; Golub, G.R.; Kenneally, R.M.; Moore, P.B.; Sands, S.P.; Throm, E.D.; Wetzel, B.A.

    1994-02-01

    This preapplication safety evaluation report (PSER) presents the results of the preapplication desip review for die Power Reactor Innovative Small Module (PRISM) liquid-mew (sodium)-cooled reactor, Nuclear Regulatory Commission (NRC) Project No. 674. The PRISM conceptual desip was submitted by the US Department of Energy in accordance with the NRC`s ``Statement of Policy for the Regulation of Advanced Nuclear Power Plants`` (51 Federal Register 24643). This policy provides for the early Commission review and interaction with designers and licensees. The PRISM reactor desip is a small, modular, pool-type, liquid-mew (sodium)-cooled reactor. The standard plant design consists of dim identical power blocks with a total electrical output rating of 1395 MWe- Each power block comprises three reactor modules, each with a thermal rating of 471 MWt. Each module is located in its own below-grade silo and is co to its own intermediate heat transport system and steam generator system. The reactors utilize a metallic-type fuel, a ternary alloy of U-Pu-Zr. The design includes passive reactor shutdown and passive decay heat removal features. The PSER is the NRC`s preliminary evaluation of the safety features in the PRISM design, including the projected research and development programs required to support the design and the proposed testing needs. Because the NRC review was based on a conceptual design, the PSER did not result in an approval of the design. Instead it identified certain key safety issues, provided some guidance on applicable licensing criteria, assessed the adequacy of the preapplicant`s research and development programs, and concluded that no obvious impediments to licensing the PRISM design had been identified.

  14. Hydrocarbon residues in tissues of sea otters (`enhydra lutris`) collected following the Exxon Valdez oil spill. Marine mammal study 6-16. Exxon Valdez oil spill state/federal natural resource damage assessment. Final report

    SciTech Connect

    Ballachey, B.E.; Kloecker, K.A.

    1997-04-01

    Ten moderately to heavily oiled sea otters were collected in Prince William Sound during the Exxon Valdez oil spill and up to seven tissues from each were analyzed for hydrocarbons. Aliphatic and aromatic hydrocarbons were detected in all tissues. Concentrations of aromatic hydrocarbons in fat samples were an order of magnitude higher than in other tissues. The patterns of distribution of these hydrocarbons suggested crude oil as the source of contamination. However, there was variation among oiled otters in the concentrations of individual hydrocarbons, which may be due to differing proximate causes of mortality and varying lengths of time and sea otters survived following oil exposure. The concentrations of both aliphatic and aromatic hydrocarbons in the tissues of the ten oiled sea otters generally were higher than in tissues from 7 sea otters with no external oiling that were collected from prince William Sound in 1989 and 1990, or from 12 sea otters collected from an area in southeast Alaska which had not experienced an oil spill.

  15. 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.

  16. 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.

  17. A rotating disk apparatus for assessing the biodegradation of polycyclic aromatic hydrocarbons transferring from a non-aqueous phase liquid to solutions of surfactant Brij 35.

    PubMed

    Bernardez, Letícia A

    2009-04-01

    A rotating disk apparatus was used to investigate the biodegradation of PAHs from non-aqueous phase liquids to solutions of Brij 35. The mass transfer of PAHs in absence of surfactant solution was not large enough to replenish the degraded PAHs. The addition of surfactant resulted in an overall enhancement of biodegradation rates compared to that observed in pure aqueous solution. This is because surfactant partition significant amount of PAHs into the bulk phase, where uptake occurs but the supply of PAHs to the aqueous phase through micellar solubilization at latter period limited biodegradation rates. It was demonstrated the relationship between biodegradation rate and surfactant dose and the mechanisms controlling the mass transfer of PAH from NAPLs. The satisfactory comparison of the experimental data with the predictions of a model, which parameters were determined from independent solubilization and dissolution experiments and based on the main assumption that the solutes must be present in the true aqueous phase to be degraded, allows us to conclude the absence of direct uptake of PAHs by bacteria.

  18. Reactions of aromatic hydrocarbons with nucleophilic reagents in liquid ammonia. VII. Direction of hydroxylation of 3-substituted (Cl, Br, I, NO/sub 2/) nitrobenzenes with potassium hydroxide

    SciTech Connect

    Malykhin, E.V.; Kolesnichenko, G.A.; Shteingarts, V.D.

    1986-09-20

    The reaction of 3-chloro-, 3-bromo-, and 3-iodonitrobenzenes with potassium hydroxide and oxygen in liquid ammonia (-33/sup 0/C) leads to the formation of nitrohalogenophenols, corresponding to substitution of the hydrogen atom at the ortho and para positions of the ring in relation to the nitro group by a hydroxy group. In the case of the last two substrates it also leads to the corresponding 2-halo-geno-3',4'-dinitrodiphenylamines. In view of the fact that substituted diphenylamines are formed under the same conditions as a result of the reaction of 3-nitro-aniline with 3-halogenonitrobenzenes it is suggested that 3-bromo- and 3-iodonitrobenzenes are partly converted into 3-nitroaniline through the intermediate formation of 3-nitrodehydrobenzene. During dehydroxylation in the absence of oxygen the proportion of the phenols corresponding to substitution of the hydrogen atom at the para position to the nitro group by the hydroxy group increases, and the degree of transformation of the initial compounds decreases. 2,4-dinitrophenol is formed with a low yield during the reaction of 1,3-nitrobenzene and potassium hydroxide in the presence of oxygen or in an atmosphere of argon.

  19. Quantification of polycyclic aromatic hydrocarbons in toasted guaraná (Paullinia cupana) by high-performance liquid chromatography with a fluorescence detector.

    PubMed

    Veiga, L L A; Amorim, H; Moraes, J; Silva, M C; Raices, R S L; Quiterio, S L

    2014-01-01

    Samples of toasted guaraná seeds with husk from Maués (Amazônia) and ten samples of different brands of guaraná powder produced in different parts of Brazil were analysed in this work, aiming to identify and quantify 16 PAHs. The samples were analysed by high-performance liquid chromatography equipped with fluorescence and UV-Vis detectors. Naphthalene was identified and quantified in the guaraná samples (0.13 and 0.78 μg kg(-1)) and both naphthalene and phenanthrene were found in two commercial guaraná powder samples (0.36-1.54 and 0.03-0.06 μg kg(-1), respectively). Considering that the average daily intake of guaraná powder is equivalent to 10 g, it can be seen that guaraná powder contains less PAHs than the limit established in European legislation for other kinds of food (CE 835/2011), that is, around 0.20 μg kg(-1) of PAHs.

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

    PubMed

    Uematsu, Yoko; Suzuki, Kumi; Ogimoto, Mami

    2016-01-01

    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.