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Sample records for catalytic coal conversion

  1. Molecular catalytic coal liquid conversion

    Energy Technology Data Exchange (ETDEWEB)

    Stock, L.M.; Yang, Shiyong [Univ. of Chicago, IL (United States)

    1995-12-31

    This research, which is relevant to the development of new catalytic systems for the improvement of the quality of coal liquids by the addition of dihydrogen, is divided into two tasks. Task 1 centers on the activation of dihydrogen by molecular basic reagents such as hydroxide ion to convert it into a reactive adduct (OH{center_dot}H{sub 2}){sup {minus}} that can reduce organic molecules. Such species should be robust withstanding severe conditions and chemical poisons. Task 2 is focused on an entirely different approach that exploits molecular catalysts, derived from organometallic compounds that are capable of reducing monocyclic aromatic compounds under very mild conditions. Accomplishments and conclusions are discussed.

  2. Studies of coupled chemical and catalytic coal conversion methods

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    Stock, L.M.; Chatterjee, K.; Cheng, C.; Ettinger, M.; Flores, F.; Jiralerspong, S.; Miyake, M.; Muntean, J.

    1991-12-01

    The objective of this research was to convert coal into a soluble substance under mild conditions. The strategy involved two steps, first to breakdown the macromolecular network of coal, and second to add hydrogen catalytically. We investigated different basic reagents that could, in priciple, break down coal`s structure and alkylation strategies that might enhance its solubility. We examined O- and C-alkylation, the importance of the strength of the base, the character of the added alkyl groups and other reaction parameters. This work provided new information concerning the way in which hydrogen bonding, polarization interactions between aromatic structures and covalent bonding could be disrupted and solubility enhanced. The objective of our research was to explore new organochromium chemistry that might be feasible for the hydrogenation of coal under mild conditions.

  3. Studies of coupled chemical and catalytic coal conversion methods

    Energy Technology Data Exchange (ETDEWEB)

    Stock, L.M.; Chatterjee, K.; Cheng, C.; Ettinger, M.; Flores, F.; Jiralerspong, S.; Miyake, M.; Muntean, J.

    1991-12-01

    The objective of this research was to convert coal into a soluble substance under mild conditions. The strategy involved two steps, first to breakdown the macromolecular network of coal, and second to add hydrogen catalytically. We investigated different basic reagents that could, in priciple, break down coal's structure and alkylation strategies that might enhance its solubility. We examined O- and C-alkylation, the importance of the strength of the base, the character of the added alkyl groups and other reaction parameters. This work provided new information concerning the way in which hydrogen bonding, polarization interactions between aromatic structures and covalent bonding could be disrupted and solubility enhanced. The objective of our research was to explore new organochromium chemistry that might be feasible for the hydrogenation of coal under mild conditions.

  4. Molecular catalytic coal liquid conversion. Quarterly progress report, [April--June 1993

    Energy Technology Data Exchange (ETDEWEB)

    Stock, L.M.; Cheng, C.; Ettinger, M.

    1993-06-30

    This phase of the project essentially consists of preparing organometallic reagents which are known or have been reported to act as homogeneous hydrogenation catalysts of aromatic hydrocarbons and studying their properties as homogeneous hydrogenation catalysts under various conditions with the ultimate objective of using these compounds to catalyze the conversion of coal liquids. With regards to this task, we have prepared two rhodium (I) catalysts. These are the dimer of dichloropentamethylcyclopentadienylrhodium, [RhCl{sub 2}(C{sub 5}Me{sub 5})], and the dimer of chloro(1,5-hexadiene) rhodium. The dimer of dichloropentamethylcyclopentadienylrhodium was prepared by stirring rhodium (III) chloride hydrate with hexamethyldewarbenzene at 65{degrees}C. It was reported to hydrogenate arenes and various substituted arenas such as aryl ethers, esters and ketones at 50{degrees} and 50 atm of dihydrogen. The dimer of chloro (1,5-hexadiene) rhodium was prepared by reacting rhodium (III) chloride hydrate with 1,5-hexadiene at 50{degrees}C for six days in water. Our second task is to investigate the chemistry of base-catalyzed hydrogenation of organic compounds with the ultimate objective of applying the chemistry behind this novel concept to the catalytic conversion of coal liquids. It is not generally known that bases such as the hydroxide ion are capable of activating dihydrogen to form ``solvated hydride`` or hydride-like species which can effect hydrogenation reactions under the appropriate conditions. Research during the first half of this century has amply demonstrated the feasibility of this concept. More recently, Klingler, Krause and Rathke studied the role of this kind of chemistry in the water-gas shift reaction. So far, only Walling and Bollyky have been the only investigators to have applied dihydrogen activation by bases to the hydrogenation of organic compounds.

  5. Catalytic Process for the Conversion of Coal-derived Syngas to Ethanol

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    James Spivery; Doug Harrison; John Earle; James Goodwin; David Bruce; Xunhau Mo; Walter Torres; Joe Allison Vis Viswanathan; Rick Sadok; Steve Overbury; Viviana Schwartz

    2011-07-29

    The catalytic conversion of coal-derived syngas to C{sub 2+} alcohols and oxygenates has attracted great attention due to their potential as chemical intermediates and fuel components. This is particularly true of ethanol, which can serve as a transportation fuel blending agent, as well as a hydrogen carrier. A thermodynamic analysis of CO hydrogenation to ethanol that does not allow for byproducts such as methane or methanol shows that the reaction: 2 CO + 4 H{sub 2} {yields} C{sub 2}H{sub 5}OH + H{sub 2}O is thermodynamically favorable at conditions of practical interest (e.g,30 bar, {approx}< 250 C). However, when methane is included in the equilibrium analysis, no ethanol is formed at any conditions even approximating those that would be industrially practical. This means that undesired products (primarily methane and/or CO{sub 2}) must be kinetically limited. This is the job of a catalyst. The mechanism of CO hydrogenation leading to ethanol is complex. The key step is the formation of the initial C-C bond. Catalysts that are selective for EtOH can be divided into four classes: (a) Rh-based catalysts, (b) promoted Cu catalysts, (c) modified Fischer-Tropsch catalysts, or (d) Mo-sulfides and phosphides. This project focuses on Rh- and Cu-based catalysts. The logic was that (a) Rh-based catalysts are clearly the most selective for EtOH (but these catalysts can be costly), and (b) Cu-based catalysts appear to be the most selective of the non-Rh catalysts (and are less costly). In addition, Pd-based catalysts were studied since Pd is known for catalyzing CO hydrogenation to produce methanol, similar to copper. Approach. The overall approach of this project was based on (a) computational catalysis to identify optimum surfaces for the selective conversion of syngas to ethanol; (b) synthesis of surfaces approaching these ideal atomic structures, (c) specialized characterization to determine the extent to which the actual catalyst has these structures, and (d) testing

  6. In Situ Catalytic Pyrolysis of Low-Rank Coal for the Conversion of Heavy Oils into Light Oils

    Directory of Open Access Journals (Sweden)

    Muhammad Nadeem Amin

    2017-01-01

    Full Text Available Lighter tars are largely useful in chemical industries but their quantity is quite little. Catalytic cracking is applied to improve the yield of light tars during pyrolysis. Consequently, in situ upgrading technique through a MoS2 catalyst has been explored in this research work. MoS2 catalyst is useful for the conversion of high energy cost into low energy cost. The variations in coal pyrolysis tar without and with catalyst were determined. Meanwhile, the obtained tar was analyzed using simulated distillation gas chromatograph and Elemental Analyzer. Consequently, the catalyst reduced the pitch contents and increased the fraction of light tar from 50 to 60 wt.% in coal pyrolysis tar. MoS2 catalyst increased the liquid yield from 18 to 33 (wt.%, db and decreased gas yield from 27 to 12 (wt.%, db compared to coal without catalyst. Moreover, it increased H content and hydrogen-to-carbon ratio by 7.9 and 3.3%, respectively, and reduced the contents of nitrogen, sulphur, and oxygen elements by 8.1%, 15.2%, and 23.9%, respectively, in their produced tars compared to coal without catalyst.

  7. Molecular catalytic coal liquid conversion. Quarterly progress report, [January--March 1993

    Energy Technology Data Exchange (ETDEWEB)

    Stock, L.M.; Cheng, C.; Ettinger, M.

    1993-03-31

    Last quarter, substantial progress has been made in the two general tasks advanced in our research proposal. The first task consists of the development of molecular homogeneous catalysts that can be used in the hydrogenation of coal liquids and in coal conversion processes. The second task concerns the activation of dihydrogen by basic catalysts in homogeneous reaction systems. With regards to the first task, we have prepared two organometallic rhodium (1) catalysts. These are the dimer of dichloropentamethylcyclopentadienylrhodium, [RhCl{sub 2}(C{sub 5}Me{sub 5})], and the dimer of chloro(1,5-hexadiene)rhodium We have subsequently investigated the hydrogenation of various aromatic organic compounds using these organometallic reagents as catalysts. Results showed that both catalysts effected the hydrogenation of the aromatic portions of a wide range of organic compounds, including aromatic hydrocarbons and aromatic compounds containing the ether group, alkyl groups, amino and carbonyl groups. However, both compounds were totally ineffective in catalyzing the hydrogenation of sulfur-containing aromatic organic compounds. Nevertheless, both rhodium catalysts successfully catalyzed the hydrogenation of naphthalene even in the presence of the coal liquids. With regards to base-activated hydrogenation of organic compounds, we have found that hydroxide and alkoxide bases are capable of activating,dihydrogen, thereby leading to the hydrogenation of phenyl-substituted alkenes. More specifically, tetrabutylammonium hydroxide, potassium tert-butoxide and potassium phenoxide were successfully used to activate dihydrogen and induce the hydrogenation of trans-stilbene. Potassium tert-butoxide was found to be slightly more effective than the other two bases in accomplishing this chemistry.

  8. Effects of low-temperature catalytic pretreatments on coal structure and reactivity in liquefaction. Final technical report, Volume 1 - effects of solvents, catalysts and temperature conditions on conversion and structural changes of low-rank coals

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    Huang, Lili [Pennsylvania State Univ., University Park, PA (United States); Schobert, Harold H. [Pennsylvania State Univ., University Park, PA (United States); Song, Chunshan [Pennsylvania State Univ., University Park, PA (United States)

    1998-01-01

    The main objectives of this project were to study the effects of low-temperature pretreatments on coal structure and their impacts on subsequent liquefaction. The effects of pretreatment temperatures, catalyst type, coal rank, and influence of solvent were examined. Specific objectives were to identify the basic changes in coal structure induced by catalytic and thermal pretreatments, and to determine the reactivity of the catalytically and thermally treated coals for liquefaction. In the original project management plan it was indicated that six coals would be used for the study. These were to include two each of bituminous, subbituminous, and lignite rank. For convenience in executing the experimental work, two parallel efforts were conducted. The first involved the two lignites and one subbituminous coal; and the second, the two bituminous coals and the remaining subbituminous coal. This Volume presents the results of the first portion of the work, studies on two lignites and one subbituminous coal. The remaining work accomplished under this project will be described and discussed in Volume 2 of this report. The objective of this portion of the project was to determine and compare the effects of solvents, catalysts and reaction conditions on coal liquefaction. Specifically, the improvements of reaction conversion, product distribution, as well as the structural changes in the coals and coal-derived products were examined. This study targeted at promoting hydrogenation of the coal-derived radicals, generated during thermal cleavage of chemical bonds, by using a good hydrogen donor-solvent and an effective catalyst. Attempts were also made in efforts to match the formation and hydrogenation of the free radicals and thus to prevent retrogressive reaction.

  9. Catalytic Conversion of Biomass

    Directory of Open Access Journals (Sweden)

    Rafael Luque

    2016-09-01

    Full Text Available Petroleum, natural gas and coal supply most of the energy consumed worldwide and their massive utilization has allowed our society to reach high levels of development in the past century.[...

  10. Catalytic conversion of biomass to fuels. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Garten, R. L.; Ushiba, K. K.; Cooper, M.; Mahawili, I.

    1978-01-01

    This report presents an assessment and perspective concerning the application of catalytic technologies to the thermochemical conversion of biomass resources to fuels. The major objectives of the study are: to provide a systematic assessment of the role of catalysis in the direct thermochemical conversion of biomass into gaseous and liquid fuels; to establish the relationship between potential biomass conversion processes and catalytic processes currently under development in other areas, with particular emphasis on coal conversion processes; and to identify promising catalytic systems which could be utilized to reduce the overall costs of fuels production from biomass materials. The report is divided into five major parts which address the above objectives. In Part III the physical and chemical properties of biomass and coal are compared, and the implications for catalytic conversion processes are discussed. With respect to chemical properties, biomass is shown to have significant advantages over coal in catalytic conversion processes because of its uniformly high H/C ratio and low concentrations of potential catalyst poisons. The physical properties of biomass can vary widely, however, and preprocessing by grinding is difficult and costly. Conversion technologies that require little preprocessing and accept a wide range of feed geometries, densities, and particle sizes appear desirable. Part IV provides a comprehensive review of existing and emerging thermochemical conversion technologies for biomass and coal. The underlying science and technology for gasification and liquefaction processes are presented.

  11. Studies of catalytic coal gasification with steam

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    Porada Stanisław

    2016-09-01

    Full Text Available One of the promising processes, belonging to the so-called clean coal technologies, is catalytic coal gasification. The addition of a catalyst results in an increased process rate, in which synthesis gas is obtained. Therefore, the subject of this research was catalytic gasification of low-ranking coal which, due to a high reactivity, meets the requirements for fuels used in the gasification process. Potassium and calcium cations in an amount of 0.85, 1.7 and 3.4% by weight were used as catalytically active substances. Isothermal measurements were performed at 900°C under a pressure of 2 MPa using steam as a gasifying agent. On the basis of kinetic curves, the performance of main gasification products as well as carbon conversion degree were determined. The performed measurements allowed the determination of the type and amount of catalyst that ensure the most efficient gasification process of the coal ‘Piast’ in an atmosphere of steam.

  12. Catalytic Conversion of Carbohydrates

    DEFF Research Database (Denmark)

    Osmundsen, Christian Mårup

    -oxygenates through thermal retro-aldol condensations. One compound, glycolaldehyde, could be prepared in yields of over 60% by this method; as this compound can potentially be used as a starting point for producing a wide range of chemicals, such as ethylene glycol or acetic acid, this process could prove...... to be an efficient initial conversion step in the utilization of biomass for chemicals production. The shift from an oil based chemical industry to one based on renewable resources is bound to happen sooner or later, however the environmental problems associated with the burning of fossil resources means......Modern civilization is dependent on oil to supply energy for power, heating and transportation and carbon for the production of the plethora of chemicals needed. Oil is however a limited resource and alternatives need to be identified before we freeze in the dark [1]. This thesis deals...

  13. Shungite carbon catalytic effect on coal treatment

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    Grigorieva, E.N.; Rozhkova, N.N. [Russian Academy of Sciences, Moscow (Russian Federation). Institute for High Temperature

    1999-07-01

    The catalytic ability of shungite carbon in reactions of coal organic matter models appeared to be due to its fullerene structure only. Transition metal sulphides present in shungite carbon are not active in the conditions of coal treatment. Shungite carbon was shown to exhibit an acceleration of thermolysis of coal and organic matter models, mainly dehydrogenation. 5 refs., 1 tabs.

  14. Catalytic conversion of light alkanes

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    Lyons, J.E.

    1992-06-30

    The second Quarterly Report of 1992 on the Catalytic Conversion of Light Alkanes reviews the work done between April 1, 1992 and June 31, 1992 on the Cooperative Agreement. The mission of this work is to devise a new catalyst which can be used in a simple economic process to convert the light alkanes in natural gas to oxygenate products that can either be used as clean-burning, high octane liquid fuels, as fuel components or as precursors to liquid hydrocarbon uwspomdon fuel. During the past quarter we have continued to design, prepare, characterize and test novel catalysts for the mild selective reaction of light hydrocarbons with air or oxygen to produce alcohols directly. These catalysts are designed to form active metal oxo (MO) species and to be uniquely active for the homolytic cleavage of the carbon-hydrogen bonds in light alkanes producing intermediates which can form alcohols. We continue to investigate three molecular environments for the active catalytic species that we are trying to generate: electron-deficient macrocycles (PHASE I), polyoxometallates (PHASE II), and regular oxidic lattices including zeolites and related structures as well as other molecular surface structures having metal oxo groups (PHASE I).

  15. Catalytic coal liquefaction. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Weller, S W

    1981-01-01

    Monolith catalysts of MoO/sub 3/-CoO-Al/sub 2/O/sub 3/ were prepared and tested for coal liquefaction in a stirred autoclave. In general, the monolith catalysts were not as good as particulate catalysts prepared on Corning alumina supports. Measurement of O/sub 2/ chemisorption and BET surface area has been made on a series of Co/Mo/Al/sub 2/O/sub 3/ catalysts obtained from PETC. The catalysts were derived from Cyanamid 1442A and had been tested for coal liquefaction in batch autoclaves and continuous flow units. MoO/sub 3/-Al/sub 2/O/sub 3/ catalysts over the loading range 3.9 to 14.9 wt % MoO/sub 3/ have been studied with respect to BET surface (before and after reduction), O/sub 2/ chemisorption at -78/sup 0/C, redox behavior at 500/sup 0/C, and activity for cyclohexane dehydrogenation at 500/sup 0/C. In connection with the fate of tin catalysts during coal liquefaction, calculations have been made of the relative thermodynamic stability of SnCl/sub 2/, Sn, SnO/sub 2/, and SnS in the presence of H/sub 2/, HCl, H/sub 2/S and H/sub 2/O. Ferrous sulfate dispersed in methylnaphthalene has been shown to be reduced to ferrous sulfide under typical coal hydroliquefaction conditions (1 hour, 450/sup 0/C, 1000 psi initial p/sub H/sub 2//). This suggests that ferrous sulfide may be the common catalytic ingredient when either (a) ferrous sulfate impregnated on powdered coal, or (b) finely divided iron pyrite is used as the catalyst. Old research on impregnated ferrous sulfate, impregnated ferrous halides, and pyrite is consistent with this assumption. Eight Co/Mo/Al/sub 2/O/sub 3/ catalysts from commercial suppliers, along with SnCl/sub 2/, have been studied for the hydrotreating of 1-methylnaphthalene (1-MN) in a stirred autoclave at 450 and 500/sup 0/C.

  16. Role of coal water mixture in utility coal conversion

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    Bhagat, N.; Butcher, T.

    1984-05-01

    To indicate the role of coal water mixtures (CWM) in utility coal conversions, the pertinent technical, economic, environmental, and regulatory factors involved in CWM conversion are reviewed. CWM technology provides an attractive option for utility companies to convert to coal. There appear to be no major technical problems in CWM production and use that cannot be overcome. Environmental considerations, however, play an important role in utilities' decisions to convert to coal. In general, coal conversions would be seriously impeded if the installation of flue gas desulfurization units cannot be avoided, as it now can because of the DOE program, and they are also inhibited by present uncertainties regarding impending acid rain regulations. Preliminary estimates of the economics of conversion seem attractive; however, site-specific evaluation is needed to justify conversion in a given situation. Although conversion to pulverized coal appears competitive with that to CWM, some non-economic factors tend to favor CWM over PC.

  17. Catalytic conversions of methyltetrahydrophthalic anhydride

    Energy Technology Data Exchange (ETDEWEB)

    Lezdin, S.Yu.; Dokuchaeva, T.G.; Sibarov, D.A.; Panfilova, N.N.; Proskuryakov, V.A.

    1987-07-10

    Catalysts with various amounts (from 2.0 to 6.0 mass %) of the active component were tested for estimation of the hydrogenating and dehydrogenating properties of palladium on alumina. Alumina-palladium catalyst with a palladium content of 5.0 mass % has the highest activity and selectivity in synthesis of 4-MPA. The yield of 4-MPA under the optical conditions found is 60-61% on the converted feed, with 100% conversion. Alumina-palladium catalyst with a palladium content of 3.0 mass % has the highest activity and selectivity in synthesis of 4-MHHPA. Under the optimal conditions found the yield of 4-MHHPA is 75-80% on the converted feed, with 100% conversion.

  18. Catalytic processes for space station waste conversion

    Science.gov (United States)

    Schoonover, M. W.; Madsen, R. A.

    1986-01-01

    Catalytic techniques for processing waste products onboard space vehicles were evaluated. The goal of the study was the conversion of waste to carbon, wash water, oxygen and nitrogen. However, the ultimate goal is conversion to plant nutrients and other materials useful in closure of an ecological life support system for extended planetary missions. The resulting process studied involves hydrolysis at 250 C and 600 psia to break down and compact cellulose material, distillation at 100 C to remove water, coking at 450 C and atmospheric pressure, and catalytic oxidation at 450 to 600 C and atmospheric pressure. Tests were conducted with a model waste to characterize the hydrolysis and coking processes. An oxidizer reactor was sized based on automotive catalytic conversion experience. Products obtained from the hydrolysis and coking steps included a solid residue, gases, water condensate streams, and a volatile coker oil. Based on the data obtained, sufficient component sizing was performed to make a preliminary comparison of the catalytic technique with oxidation for processing waste for a six-man spacecraft. Wet oxidation seems to be the preferred technique from the standpoint of both component simplicity and power consumption.

  19. Catalytic coal gasification: an emerging technology.

    Science.gov (United States)

    Hirsch, R L; Gallagher, J E; Lessard, R R; Wesslhoft, R D

    1982-01-08

    Catalytic coal gasification is being developed as a more efficient and less costly approach to producing methane from coal. With a potassium catalyst all the reactions can take place at one temperature, so that endothermic and exothermic reactions can be integrated in a single reactor. A key aspect of the concept involves continuous recycling of product carbon monoxide and hydrogen to the gasifier following separation of methane. Development of the process has advanced steadily since the basic concept was proposed in 1971. A 23-day demonstration run was recently completed in a process development unit with a coal feed rate of 1 ton per day. The next major step in the program will be to design and construct a large pilot plant to bring the technology to commercial readiness in the late 1980's.

  20. Study of coal conversion in an arc plasma jet

    Energy Technology Data Exchange (ETDEWEB)

    Xie, K.C.; Lu, Y.K.; Tian, Y.J.; Wang, D.Z. [Taiyuan University of Technology, Taiyuan (China)

    2002-12-01

    Coal conversion in arc plasma with an initial temperature of 3700 K is complex; a new conversion mechanism is put forward in this article. The functions of pyrolysis and the interaction of active species containing plasma jets are the main factors for coal conversion under these conditions. This study indicates that when the coal feed rate is lower than 2.0 g/s, both pyrolysis and active species have evident contribution to coal conversion; the pyrolysis controls the coal conversion and the function of active species is very weak. It is also found that the coal feed rate has a large influence on coal conversion and the production of gas components.

  1. Porous media for catalytic renewable energy conversion

    Science.gov (United States)

    Hotz, Nico

    2012-05-01

    A novel flow-based method is presented to place catalytic nanoparticles into a reactor by sol-gelation of a porous ceramic consisting of copper-based nanoparticles, silica sand, ceramic binder, and a gelation agent. This method allows for the placement of a liquid precursor containing the catalyst into the final reactor geometry without the need of impregnating or coating of a substrate with the catalytic material. The so generated foam-like porous ceramic shows properties highly appropriate for use as catalytic reactor material, e.g., reasonable pressure drop due to its porosity, high thermal and catalytic stability, and excellent catalytic behavior. The catalytic activity of micro-reactors containing this foam-like ceramic is tested in terms of their ability to convert alcoholic biofuel (e.g. methanol) to a hydrogen-rich gas mixture with low concentrations of carbon monoxide (up to 75% hydrogen content and less than 0.2% CO, for the case of methanol). This gas mixture is subsequently used in a low-temperature fuel cell, converting the hydrogen directly to electricity. A low concentration of CO is crucial to avoid poisoning of the fuel cell catalyst. Since conventional Polymer Electrolyte Membrane (PEM) fuel cells require CO concentrations far below 100 ppm and since most methods to reduce the mole fraction of CO (such as Preferential Oxidation or PROX) have CO conversions of up to 99%, the alcohol fuel reformer has to achieve initial CO mole fractions significantly below 1%. The catalyst and the porous ceramic reactor of the present study can successfully fulfill this requirement.

  2. Coal conversion. 1977 technical report

    Energy Technology Data Exchange (ETDEWEB)

    None

    1978-06-01

    The status and progress in US DOE's projects in coal gasification, liquefaction, and fluidized-bed combustion are reviewed with financing, flowsheets, history, progress and status of each (57 projects). (LTN)

  3. Coal conversion. 1979 technical report

    Energy Technology Data Exchange (ETDEWEB)

    None

    1980-09-01

    Individual reports are made on research programs which are being conducted by various organizations and institutions for the commercial development of processes for converting coal into products that substitute for these derived from oil and natural gas. Gasification, liquefaction, and demonstration processes and plants are covered. (DLC)

  4. Catalytic coal conversion support: use of laser flash-pyrolysis for structural analysis. Progress report, April 15, 1979-September 30, 1981

    Energy Technology Data Exchange (ETDEWEB)

    Verzino, Jr, W J; Rofer-DePoorter, C K; Hermes, R E

    1982-03-01

    Untreated Fruitland subbituminous coal and Fruitland coal treated with several gasification catalysts were pyrolyzed with both Nd-glass and CO/sub 2/ lasers (1.06-..mu..m and 10.6-..mu..m wavelengths, respectively) to give both gaseous and intermediate-molecular weight products, which were analyzed by gas chromatography (GC) and gas chromatography-mass spectrometry (GC-MS). The catalysts used were AlCl/sub 3/, K/sub 2/H/sub 2/Sb/sub 2/O/sub 7/, CoCl/sub 2/, PbCl/sub 2/, Pb(NO/sub 3/)/sub 2/, Na/sub 2/Pb(OH)/sub 6/, Na/sub 2/MoO/sub 4/, NiCl/sub 2/, K/sub 2/CO/sub 3/, KHCO/sub 3/, Na/sub 2/CO/sub 3/, NaHCO/sub 3/, Na/sub 2/Ti/sub 3/O/sub 7/, NaVO/sub 3/, ZnCl/sub 2/, and NaZn(OH)/sub 3/. Gaseous products were analyzed from the Nd-glass laser pyrolysis; of the various catalysts, ZnCl/sub 2/ was found to affect N/sub 2/ production during pyrolysis most significantly. Intermediate products were analyzed from the CO/sub 2/ laser pyrolysis; product distribution was found to depend upon particle size (and consequent thermal history in pyrolysis) as well as on catalyst and heat treatment. Pyrolysis products could not be correlated in a statistically reliable way with coal or char structure. A supercritical extraction method with a Soxhlet extractor inside a pressure vessel was developed for liquid CO/sub 2/ as extractant. Gases evolved during processing of the coal-catalyst mixtures were analyzed by GC for several of the catalysts.

  5. Kinetics of coal conversion in supercritical water

    Energy Technology Data Exchange (ETDEWEB)

    Anatoli A. Vostrikov; Sergey A. Psarov; Dmitri Yu. Dubov; Oxana N. Fedyaeva; Mikhail Ya. Sokol [Siberian Branch of the Russian Academy of Sciences, Novosibirsk (Russian Federation). Institute of Thermophysics

    2007-09-15

    Conversion of the coal particle pack in supercritical water (SCW) was studied in the semibatch reactor under the pressure of P = 30 MPa, in the temperature range of T = 500-750{sup o}C, and in the reaction time of t = 60-720 s. The experimental results were analyzed within the framework of homogeneous, nonreacted core, and random pore models. The quantitative composition of conversion products was determined. Dependences of the conversion rate on the degree of coal conversion, reaction time, and temperature were described in an assumption of the first-order reaction and Arrhenius dependence. It was found that activation energy of conversion is E = 103 kJ/mol and the pre-exponential factor is A{sub 0} = 1.3 x 10{sup 3.1} s{sup -1}. It was revealed that coal gasification in SCW without oxidants is the weakly endothermic process. The addition of CO{sub 2} into SCW decreases the conversion rate and increases the CO yield. 20 refs., 8 figs.

  6. Materials for coal conversion and utilization

    Energy Technology Data Exchange (ETDEWEB)

    1980-01-01

    The Fifth Annual Conference on Materials for Coal Conversion and Utilization was held October 7-9, 1980, at the National Bureau of Standards, Gaithersburg, Maryland. Sixty-six papers have been entered individually into ERA and EDB; two had been entered previously from other sources. (LTN)

  7. Balanced program plan. Volume IV. Coal conversion

    Energy Technology Data Exchange (ETDEWEB)

    Richmond, C. R.; Reichle, D. E.; Gehrs, C. W.

    1976-05-01

    This document contains a description of the biomedical and environmental research necessary to ensure the timely attainment of coal conversion technologies amenable to man and his environment. The document is divided into three sections. The first deals with the types of processes currently being considered for development; the data currently available on composition of product, process and product streams, and their potential effects; and problems that might arise from transportation and use of products. Section II is concerned with a description of the necessary research in each of the King-Muir categories, while the third section presents the research strategies necessary to assess the potential problems at the conversion plant (site specific) and those problems that might effect the general public and environment as a result of the operation of large-scale coal conversion plants. (auth)

  8. Enzymantic Conversion of Coal to Liquid Fuels

    Energy Technology Data Exchange (ETDEWEB)

    Richard Troiano

    2011-01-31

    The work in this project focused on the conversion of bituminous coal to liquid hydrocarbons. The major steps in this process include mechanical pretreatment, chemical pretreatment, and finally solubilization and conversion of coal to liquid hydrocarbons. Two different types of mechanical pretreatment were considered for the process: hammer mill grinding and jet mill grinding. After research and experimentation, it was decided to use jet mill grinding, which allows for coal to be ground down to particle sizes of 5 {mu}m or less. A Fluid Energy Model 0101 JET-O-MIZER-630 size reduction mill was purchased for this purpose. This machine was completed and final testing was performed on the machine at the Fluid Energy facilities in Telford, PA. The test results from the machine show that it can indeed perform to the required specifications and is able to grind coal down to a mean particle size that is ideal for experimentation. Solubilization and conversion experiments were performed on various pretreated coal samples using 3 different approaches: (1) enzymatic - using extracellular Laccase and Manganese Peroxidase (MnP), (2) chemical - using Ammonium Tartrate and Manganese Peroxidase, and (3) enzymatic - using the live organisms Phanerochaete chrysosporium. Spectral analysis was used to determine how effective each of these methods were in decomposing bituminous coal. After analysis of the results and other considerations, such as cost and environmental impacts, it was determined that the enzymatic approaches, as opposed to the chemical approaches using chelators, were more effective in decomposing coal. The results from the laccase/MnP experiments and Phanerochaete chrysosporium experiments are presented and compared in this final report. Spectra from both enzymatic methods show absorption peaks in the 240nm to 300nm region. These peaks correspond to aromatic intermediates formed when breaking down the coal structure. The peaks then decrease in absorbance over time

  9. Biological conversion of coal synthesis gas to methane

    Energy Technology Data Exchange (ETDEWEB)

    Barik, S.; Corder, R.E.; Clausen, E.C.; Gaddy, J.L.

    1987-09-01

    High temperatures and pressures are required, and therefore, high costs incurred during catalytic upgrading of coal synthesis gas to methane. Thus, the feasibility of biological reactions in converting synthesis gas to methane has been demonstrated in mixed and pure cultures. Complete conversion has been achieved in 2 hours with a mixed culture, and 45 minutes to 1.5 hours in pure cultures of P. productus and Methanothrix sp.. Typical sulfur levels involved during the process are found not to inhibit the bacteria and so sulfur does not have to be removed prior to biomethanation. Preliminary economic analyses indicate that coal gas may be biologically methanated for 50-60 cents/million Btu. Further studies with pure culture bacteria and increased pressure are expected to enhance biomethanation economics.

  10. Biological conversion of coal gas to methane

    Energy Technology Data Exchange (ETDEWEB)

    Barik, S.; Vega, J.L.; Clausen, E.C.; Gaddy, J.L.

    1988-08-01

    Biological conversion of low-Btu coal synthesis gas to higher Btu methane was demonstrated using both pure co-cultures and/or adapted-mixed anaerobic bacteria. Peptostreptococcus productus metabolized coal gas to mainly acetate and CO/sub 2/. The co-cultures containing methanogens converted these products to methane. In mixed culture studies, CH/sub 4/ and small amounts of acetate were produced. Reactor studies using stirred-tank and immobilized cell reactors exhibited excellent potential to convert CO, CO/sub 2/ and H/sub 2/ to methane at higher gas flow rates. Gas retention times ranging from 0.7 to 2 hours and high agitation were required for 90 percent CO conversion in these systems. This paper also illustrates the potential of biological methanation and demonstrates the need for good mass transfer in converting gas phase substrates. 21 refs., 1 fig., 7 tabs.

  11. Materials for coal conversion and utilization

    Energy Technology Data Exchange (ETDEWEB)

    None,

    1981-01-01

    The Sixth annual conference on materials for coal conversion and utilization was held October 13-15, 1981 at the National Bureau of Standards Gaithersburg, Maryland. It was sponsored by the US Department of Energy, the Electric Power Research Institute, the Gas Research Institute and the National Bureau of Standards. Fifty-eight papers from the proceedings have been entered individually into EDB and ERA; four papers had been entered previously from other sources. (LTN)

  12. A Review of Thermal Co-Conversion of Coal and Biomass/Waste

    Directory of Open Access Journals (Sweden)

    Aime Hilaire Tchapda

    2014-02-01

    Full Text Available Biomass is relatively cleaner than coal and is the only renewable carbon resource that can be directly converted into fuel. Biomass can significantly contribute to the world’s energy needs if harnessed sustainably. However, there are also problems associated with the thermal conversion of biomass. This paper investigates and discusses issues associated with the thermal conversion of coal and biomass as a blend. Most notable topics reviewed are slagging and fouling caused by the relatively reactive alkali and alkaline earth compounds (K2O, Na2O and CaO found in biomass ash. The alkali and alkaline earth metals (AAEM present and dispersed in biomass fuels induce catalytic activity during co-conversion with coal. The catalytic activity is most noticeable when blended with high rank coals. The synergy during co-conversion is still controversial although it has been theorized that biomass acts like a hydrogen donor in liquefaction. Published literature also shows that coal and biomass exhibit different mechanisms, depending on the operating conditions, for the formation of nitrogen (N and sulfur species. Utilization aspects of fly ash from blending coal and biomass are discussed. Recommendations are made on pretreatment options to increase the energy density of biomass fuels through pelletization, torrefaction and flash pyrolysis to reduce transportation costs.

  13. Trends and Challenges in Catalytic Biomass Conversion

    DEFF Research Database (Denmark)

    Osmundsen, Christian Mårup; Egeblad, Kresten; Taarning, Esben

    2013-01-01

    The conversion of biomass to the plethora of chemicals used in modern society is one of the major challenges of the 21st century. Due to the significant differences between biomass resources and the current feedstock, crude oil, new technologies need to be developed encompassing all steps...... in the value chain, from pretreatment to purification. Heterogeneous catalysis is at the heart of the petrochemical refinery and will likely play an equally important role in the future biomass-based chemical industry. Three potentially important routes to chemicals from biomass are highlighted in this chapter....... The conversion of biomass-derived substrates, such as glycerol, by hydrogenolysis to the important chemicals ethylene glycol and propane diols. Secondly, the conversion of carbohydrates by Lewis acidic zeolites to yield alkyl lactates, and finally the conversion of lignin, an abundant low value source of biomass...

  14. Zeolitic catalytic conversion of alochols to hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Narula, Chaitanya K.; Davison, Brian H.; Keller, Martin

    2017-01-03

    A method for converting an alcohol to a hydrocarbon, the method comprising contacting said alcohol with a metal-loaded zeolite catalyst at a temperature of at least 100.degree. C. and up to 550.degree. C., wherein said alcohol can be produced by a fermentation process, said metal is a positively-charged metal ion, and said metal-loaded zeolite catalyst is catalytically active for converting said alcohol to said hydrocarbon.

  15. Catalytic conversion of ethanol on H-Y zeolite

    Directory of Open Access Journals (Sweden)

    Čegar Nedeljko

    2005-01-01

    Full Text Available The catalytic activity of the H-form of synthetic zeolite NaY was examined in this study. The catalytic activity was determined according to the rate of ethanol conversion in a gas phase in the static system. In the conversion of ethanol on synthetic NaY zeolite at 585, 595, and 610 K, on which the reaction develops at an optimal rate, ethene and diethyl ether are evolved in approximately the same quantity. After transforming the NaY zeolite into the H-form, its catalytic activity was extremely increases so, the reaction develops at a significantly lower temperature with a very large increase in the reaction rate. The distribution of the products also changes, so that at lower temperatures diethyl ether is elvolved in most cases, and the development of ethene is favored at higher ones, and after a certain period of time there is almost complete conversion of ethanol into ethene. The increase in catalytic activity, as well as the change of selectivity of conversion of ethanol on the H-form of zeolite, is the result of removing Na+ cations in the NaY zeolite, so that more acidic catalyst is obtained which contains a number of acidic catalytically active centers, as well as a more powerful one compared to the original NaY zeolite.

  16. Selective solvent absorption in coal conversion

    Energy Technology Data Exchange (ETDEWEB)

    Larsen, J.W.; Lapucha, A.; Lazarov, L.; Amui, J.

    1992-04-01

    The objectives of this project are: (1) to determine the importance of the presence of added hydrogen donor compounds within the coal in the first stage of direct liquefaction processes; and (2) to determine the composition of the solvent absorbed by and present within the coal in the first stage of direct coal liquefaction.

  17. Catalytic spectrophotometric determination of iodine in coal by pyrohydrolysis decomposition

    Energy Technology Data Exchange (ETDEWEB)

    Wu Daishe [School of Environmental Science and Engineering, Nanchang University, Nanchang 330031 (China); Institute of Geographic Sciences and Resources Research, CAS, Beijing 100101 (China)], E-mail: dswu@ncu.edu.cn; Deng Haiwen [School of Environmental Science and Engineering, Nanchang University, Nanchang 330031 (China); Wang Wuyi [Institute of Geographic Sciences and Resources Research, CAS, Beijing 100101 (China); Xiao Huayun [School of Environmental Science and Engineering, Nanchang University, Nanchang 330031 (China)

    2007-10-10

    A method for the determination of iodine in coal using pyrohydrolysis for sample decomposition was proposed. A pyrohydrolysis apparatus system was constructed, and the procedure was designed to burn and hydrolyse coal steadily and completely. The parameters of pyrohydrolysis were optimized through the orthogonal experimental design. Iodine in the absorption solution was evaluated by the catalytic spectrophotometric method, and the absorbance at 420 nm was measured by a double-beam UV-visible spectrophotometer. The limit of detection and quantification of the proposed method were 0.09 {mu}g g{sup -1} and 0.29 {mu}g g{sup -1}, respectively. After analysing some Chinese soil reference materials (SRMs), a reasonable agreement was found between the measured values and the certified values. The accuracy of this approach was confirmed by the analysis of eight coals spiked with SRMs with an indexed recovery from 94.97 to 109.56%, whose mean value was 102.58%. Six repeated tests were conducted for eight coal samples, including high sulfur coal and high fluorine coal. A good repeatability was obtained with a relative standard deviation value from 2.88 to 9.52%, averaging 5.87%. With such benefits as simplicity, precision, accuracy and economy, this approach can meet the requirements of the limits of detection and quantification for analysing iodine in coal, and hence it is highly suitable for routine analysis.

  18. Recent Advances in Catalytic Conversion of Ethanol to Chemicals

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Junming; Wang, Yong

    2014-04-30

    With increased availability and decreased cost, ethanol is potentially a promising platform molecule for the production of a variety of value-added chemicals. In this review, we provide a detailed summary of recent advances in catalytic conversion of ethanol to a wide range of chemicals and fuels. We particularly focus on catalyst advances and fundamental understanding of reaction mechanisms involved in ethanol steam reforming (ESR) to produce hydrogen, ethanol conversion to hydrocarbons ranging from light olefins to longer chain alkenes/alkanes and aromatics, and ethanol conversion to other oxygenates including 1-butanol, acetaldehyde, acetone, diethyl ether, and ethyl acetate.

  19. Atmospheric methanol measurement using selective catalytic methanol to formaldehyde conversion

    Directory of Open Access Journals (Sweden)

    S. J. Solomon

    2005-01-01

    Full Text Available A novel atmospheric methanol measurement technique, employing selective gas-phase catalytic conversion of methanol to formaldehyde followed by detection of the formaldehyde product, has been developed and tested. The effects of temperature, gas flow rate, gas composition, reactor-bed length, and reactor-bed composition on the methanol conversion efficiency of a molybdenum-rich, iron-molybdate catalyst [Mo-Fe-O] were studied. Best results were achieved using a 1:4 mixture (w/w of the catalyst in quartz sand. Optimal methanol to formaldehyde conversion (>95% efficiency occurred at a catalyst housing temperature of 345°C and an estimated sample-air/catalyst contact time of <0.2 seconds. Potential interferences arising from conversion of methane and a number of common volatile organic compounds (VOC to formaldehyde were found to be negligible under most atmospheric conditions and catalyst housing temperatures. Using the new technique, atmospheric measurements of methanol were made at the University of Bremen campus from 1 to 15 July 2004. Methanol mixing ratios ranged from 1 to 5 ppb with distinct maxima at night. Formaldehyde mixing ratios, obtained in conjunction with methanol by periodically bypassing the catalytic converter, ranged from 0.2 to 1.6 ppb with maxima during midday. These results suggest that selective, catalytic methanol to formaldehyde conversion, coupled with existing formaldehyde measurement instrumentation, is an inexpensive and effective means for monitoring atmospheric methanol.

  20. Atmospheric methanol measurement using selective catalytic methanol to formaldehyde conversion

    Directory of Open Access Journals (Sweden)

    S. J. Solomon

    2005-05-01

    Full Text Available A novel atmospheric methanol measurement technique, employing selective gas-phase catalytic conversion of methanol to formaldehyde followed by detection of the formaldehyde product, has been developed and tested. The effects of temperature, gas flow rate, gas composition, reactor-bed length, and reactor-bed composition on the methanol conversion efficiency of a molybdenum-rich, iron-molybdate catalyst [Mo-Fe-O] were studied. Best results were achieved using a 1:4 mixture (w/w of the catalyst in quartz sand. Optimal methanol to formaldehyde conversion (>95% efficiency occurred at a catalyst housing temperature of 345°C and an estimated sample-air/catalyst contact time of <0.2 s. Potential interferences arising from conversion of methane and a number of common volatile organic compounds (VOC to formaldehyde were found to be negligible under most atmospheric conditions and catalyst housing temperatures. Using the new technique, atmospheric measurements of methanol were made at the University of Bremen campus from 1 to 15 July 2004. Methanol mixing ratios ranged from 1 to 5 ppb with distinct maxima at night. Formaldehyde mixing ratios, obtained in conjunction with methanol by periodically bypassing the catalytic converter, ranged from 0.2 to 1.6 ppb with maxima during midday. These results suggest that selective, catalytic methanol to formaldehyde conversion, coupled with existing formaldehyde measurement instrumentation, is an inexpensive and effective means for monitoring atmospheric methanol.

  1. Catalytic Conversion of Methanol by Oxidative Dehydrogenation

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    This study investigates the effects of addition of oxygen on the oxidative dehydrogenation (ODH) of methanol when a fluorotetrasilicic mica ion-exchanged with palladium (Pd2+-TSM) was used as the catalyst. The reaction proceeded at a very low temperature in the presence of oxygen, and HCOOCH3 was obtained at high selectivity. By calculating the equilibrium conversion, it has been shown that substantial ODH took place for HCOOCH3 production. Consequently, this reaction would make dehydrogenation the dominant reaction at equilibrium. Not all the H dissociated from CH3OH was converted to H2O by oxidation. It has been shown that the H2O was not produced from oxidative dehydrogenation by the direct reaction of CH3OH and O2 when an attempt was made to carry out oxidative dehydrogenation using an isotope oxygen trace method in the gas phase. Therefore, when CH3OH was converted to CO2 and dehydrogenated to HCOOCH3, the C-O bonds were not dissociated.

  2. Catalytic Conversion of Cellulose to Levulinic Acid by Metal Chlorides

    Directory of Open Access Journals (Sweden)

    Beixiao Zhang

    2010-08-01

    Full Text Available The catalytic performance of various metal chlorides in the conversion of cellulose to levulinic acid in liquid water at high temperatures was investigated. The effects of reaction parameters on the yield of levulinic acid were also explored. The results showed that alkali and alkaline earth metal chlorides were not effective in conversion of cellulose, while transition metal chlorides, especially CrCl3, FeCl3 and CuCl2 and a group IIIA metal chloride (AlCl3, exhibited high catalytic activity. The catalytic performance was correlated with the acidity of the reaction system due to the addition of the metal chlorides, but more dependent on the type of metal chloride. Among those metal chlorides, chromium chloride was found to be exceptionally effective for the conversion of cellulose to levulinic acid, affording an optimum yield of 67 mol % after a reaction time of 180 min, at 200 °C, with a catalyst dosage of 0.02 M and substrate concentration of 50 wt %. Chromium metal, most of which was present in its oxide form in the solid sample and only a small part in solution as Cr3+ ion, can be easily separated from the resulting product mixture and recycled. Finally, a plausible reaction scheme for the chromium chloride catalyzed conversion of cellulose in water was proposed.

  3. Study on acetylene preparation from coal conversion directly by plasma

    Energy Technology Data Exchange (ETDEWEB)

    Bao, W.; Lu, Y.; Cao, Q.; Xie, K. [Taiyuan University of Technology, Taiyuan (China)

    2004-10-01

    To develop an innovative method for directly converting coal into an important chemical acetylene, arc plasma technology was applied to the direct conversion of coal. The powdered coal from Datong was injected into a hydrogen-enriched plasma reactor for pyrolysis. The results show that the coal conversion and the acetylene yield and the special energy consumption (SEC) of acetylene are decreased as coal feed rate is increased, but the concentration of acetylene in production gas is increased. The yield of acetylene is not obviously affected by the formation of CO in production gas. Since oxygen can compete with the active atomic carbon, therefore, the high content oxygen in coal is disadvantageous to the formation of acetylene. Under the experimental conditions selected, the coal conversion rate reach 38.42%, the concentration of acetylene in product gas is 9.30% and the selectivity of acetylene in hydrocarbon is above 70% when the coal fed is 5.0 g/s. 10 refs., 3 figs., 1 tab.

  4. Microbial conversion of coals to clean fuel forms

    Energy Technology Data Exchange (ETDEWEB)

    Barik, S.; Isbister, J.; Hawley, B.; Forgacs, T.; Reed, L.; Anspach, G.; Middaugh, T.

    1988-01-01

    Anaerobic cultures have been used for the production of methane and alcohols from coal. Cultures were adapted from natural inocula collected from sources such as sewage sludge and horse manure. A 1% (w/v) slurry of leonardite, lignite, or subbituminous coal was used in the incubations. Methane was produced from all cultures, including some untreated coals, to a greater extent than in control cultures. Over several months of adaptation, methane production capacity increased considerably. Volatile fatty acids (VFAs) were identified as intermediates in the conversion of coal to methane. A proposed scheme for the conversion is breakdown of the coal polymer by a series of organisms and metabolism of the fragments to methane precursors such as VFAs. A mixture of short chain alcohols was produced by cultures grown in the presence of methane inhibitors. These cultures after prolonged adaptation show potential for use in larger scale bioreactors for the production of gaseous and liquid fuels.

  5. Conversion of Low-Rank Wyoming Coals into Gasoline by Direct Liquefaction

    Energy Technology Data Exchange (ETDEWEB)

    Polyakov, Oleg

    2013-12-31

    Under the cooperative agreement program of DOE and funding from Wyoming State’s Clean Coal Task Force, Western Research Institute and Thermosolv LLC studied the direct conversion of Wyoming coals and coal-lignin mixed feeds into liquid fuels in conditions highly relevant to practice. During the Phase I, catalytic direct liquefaction of sub-bituminous Wyoming coals was investigated. The process conditions and catalysts were identified that lead to a significant increase of desirable oil fraction in the products. The Phase II work focused on systematic study of solvothermal depolymerization (STD) and direct liquefaction (DCL) of carbonaceous feedstocks. The effect of the reaction conditions (the nature of solvent, solvent/lignin ratio, temperature, pressure, heating rate, and residence time) on STD was investigated. The effect of a number of various additives (including lignin, model lignin compounds, lignin-derivable chemicals, and inorganic radical initiators), solvents, and catalysts on DCL has been studied. Although a significant progress has been achieved in developing solvothermal depolymerization, the side reactions – formation of considerable amounts of char and gaseous products – as well as other drawbacks do not render aqueous media as the most appropriate choice for commercial implementation of STD for processing coals and lignins. The trends and effects discovered in DCL point at the specific features of liquefaction mechanism that are currently underutilized yet could be exploited to intensify the process. A judicious choice of catalysts, solvents, and additives might enable practical and economically efficient direct conversion of Wyoming coals into liquid fuels.

  6. Coal liquefaction and gas conversion contractors review conference: Proceedings

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1995-11-01

    This volume contains 55 papers presented at the conference. They are divided into the following topical sections: Direct liquefaction; Indirect liquefaction; Gas conversion (methane conversion); and Advanced research liquefaction. Papers in this last section deal mostly with coprocessing of coal with petroleum, plastics, and waste tires, and catalyst studies. Selected papers are indexed separately for inclusion in the Energy Science and Technology Database.

  7. Heterogeneous kinetic modeling of the catalytic conversion of cycloparaffins

    Science.gov (United States)

    Al-Sabawi, Mustafa N.

    The limited availability of high value light hydrocarbon feedstocks along with the rise in crude prices has resulted in the international recognition of the vast potential of Canada's oil sands. With the recent expansion of Canadian bitumen production come, however, many technical challenges, one of which is the significant presence of aromatics and cycloparaffins in bitumen-derived feedstocks. In addition to their negative environmental impact, aromatics limit fluid catalytic cracking (FCC) feedstock conversion, decrease the yield and quality of valuable products such as gasoline and middle distillates, increase levels of polyaromatic hydrocarbons prone to form coke on the catalyst, and ultimately compromise the FCC unit performance. Although cycloparaffins do not have such negative impacts, they are precursors of aromatics as they frequently undergo hydrogen transfer reactions. However, cycloparaffin cracking chemistry involves other competing reactions that are complex and need much investigation. This dissertation provides insights and understanding of the fundamentals of the catalytic cracking of cycloparaffins using carefully selected model compounds such as methylcyclohexane (MCH) and decalin. Thermal and catalytic cracking of these cycloparaffins on FCC-type catalysts are carried out using the CREC Riser Simulator under operating conditions similar to those of the industrial FCC units in terms of temperature, reaction time, reactant partial pressure and catalyst-to-hydrocarbon ratio. The crystallite size of the supported zeolites is varied between 0.4 and 0.9 microns, with both activity and selectivity being monitored. Catalytic conversions ranged between 4 to 16 wt% for MCH and between 8 to 27 wt% for decalin. Reaction pathways of cycloparaffins are determined, and these include ring-opening, protolytic cracking, isomerization, hydrogen transfer and transalkylation. The yields and selectivities of over 60 and 140 products, formed during MCH and decalin

  8. Coal conversion. 1978 technical report. [US DOE

    Energy Technology Data Exchange (ETDEWEB)

    None

    1979-09-01

    The United States has more energy available in coal than in petroleum, natural gas, oil shale, and tar sands combined. Nationwide energy shortages, together with the availability of abundant coal reserves, make commercial production of synthetic fuels from coal vital to the Nation's total supply of clean energy. In response to this need, the Division of Fossil Fuel Processing - US Department of Energy is conducting a research, development and demonstration program to provide technology that will permit rapid commercialization of processes for converting coal into products that substitute for those derived from oil and natural gas. These substitute fuels include crude oil, fuel oil and distillates; chemical feedstocks; pipeline quality and fuel gas; and other products such as char that may be useful in energy production.

  9. Catalytic gasification of char from co-pyrolysis of coal and biomass

    Energy Technology Data Exchange (ETDEWEB)

    Zhu, Wenkui [State key Laboratory of Multi-phase Complex system, the Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100080 (China); Graduate University, Chinese Academy of Sciences, Beijing 100080 (China); Song, Wenli; Lin, Weigang [State key Laboratory of Multi-phase Complex system, the Institute of Process Engineering, Chinese Academy of Sciences, Beijing 100080 (China)

    2008-09-15

    The catalytic gasification of char from co-pyrolysis of coal and wheat straw was studied. Alkali metal salts, especially potassium salts, are considered as effective catalysts for carbon gasification by steam and CO{sub 2}, while too expensive for industry application. The herbaceous type of biomass, which has a high content of potassium, may be used as an inexpensive source of catalyst by co-processing with coal. The reactivity of chars from co-pyrolysis of coal and straw was experimentally examined. The chars were prepared in a spout-entrained reactor with different ratios of coal to straw. The gasification characteristics of chars were measured by thermogravimetric analysis (TGA). The co-pyrolysis chars revealed higher gasification reactivity than that of char from coal, especially at high level of carbon conversion. The influence of the alkali in the char and the pyrolysis temperature on the reactivity of co-pyrolysis char was investigated. The experimental results show that the co-pyrolysis char prepared at 750 C have the highest alkali concentration and reactivity. (author)

  10. Conversion of Coal Mine Gas to LNG

    Energy Technology Data Exchange (ETDEWEB)

    None, None

    2016-02-05

    This project evolved from a 1995, DOE-NETL competitive solicitation for practical CMM capture and utilization concepts. Appalachian Pacific was one of three companies selected to proceed with the construction and operation of a cost-shared demonstration plant. In the course of trying to proceed with this demonstration plant, AP examined several liquefaction technologies, discussed obtaining rights to coal mine methane with a number of coal companies, explored marketing potential with a wide variety of customers in many sections of the United States, studied in great detail the impact of a carbon credit exchange, and developed a suite of analytical tools with which to evaluate possible project options. In the end, the newness of the product, reluctance on the part of the coal companies to venture away from time tested practices, difficulty with obtaining financing, the failure of a carbon credit market to develop and the emergence of shale derived gas production prevented a demonstration plant from being built.

  11. Survey of industrial coal conversion equipment capabilities: rotating components

    Energy Technology Data Exchange (ETDEWEB)

    Williams, W. R.; Horton, J. R.; Boudreau, W. F.; Siman-Tov, M.

    1978-04-01

    At the request of the Major Facilities Project Management Division of the Energy Research and Development Administration, Fossil Energy Division, a study was undertaken to determine the capabilities of U.S. industry to supply the rotating equipment needed for future coal conversion facilities. Furthermore, problem areas were to be identified and research and development needs determined for producing advanced designs of the required equipment: Pumps, compressors, hydraulic turbines, and gas expanders. It has been concluded that equipment for essentially all clean-stream applications likely to be encountered in coal conversion facilities is generally available except high-pressure oxygen compressors. These oxygen compressors as well as slurry pumps need to be developed or significantly upgraded. Also, fans and blower for dirty-gas streams need developmental work, as do expanders for high-temperature service. Hydraulic turbines, which were not specified but which might be used for slurry applications in future coal conversion plants, are not available.

  12. Catalytic conversion of methane to methanol using Cu-zeolites.

    Science.gov (United States)

    Alayon, Evalyn Mae C; Nachtegaal, Maarten; Ranocchiari, Marco; van Bokhoven, Jeroen A

    2012-01-01

    The conversion of methane to value-added liquid chemicals is a promising answer to the imminent demand for fuels and chemical synthesis materials in the advent of a dwindling petroleum supply. Current technology requires high energy input for the synthesis gas production, and is characterized by low overall selectivity, which calls for alternative reaction routes. The limitation to achieve high selectivity is the high C-H bond strength of methane. High-temperature reaction systems favor gas-phase radical reactions and total oxidation. This suggests that the catalysts for methane activation should be active at low temperatures. The enzymatic-inspired metal-exchanged zeolite systems apparently fulfill this need, however, methanol yield is low and a catalytic process cannot yet be established. Homogeneous and heterogeneous catalytic systems have been described which stabilize the intermediate formed after the first C-H activation. The understanding of the reaction mechanism and the determination of the active metal sites are important for formulating strategies for the upgrade of methane conversion catalytic technologies.

  13. Economics of coal conversion processing. Advances in coal gasification: support research. Advances in coal gasification: process development and analysis

    Energy Technology Data Exchange (ETDEWEB)

    1978-01-01

    The fall meeting of the American Chemical Society, Division of Fuel Chemistry, was held at Miami Beach, Florida, September 10-15, 1978. Papers involved the economics of coal conversion processing and advances in coal gasification, especially support research and process development and analysis. Fourteen papers have been entered individually into EDB and ERA; three papers had been entered previously from other sources. (LTN)

  14. Catalytic conversion of methane: Carbon dioxide reforming and oxidative coupling

    KAUST Repository

    Takanabe, Kazuhiro

    2012-01-01

    Natural gas conversion remains one of the essential technologies for current energy needs. This review focuses on the mechanistic aspects of the development of efficient and durable catalysts for two reactions, carbon dioxide reforming and the oxidative coupling of methane. These two reactions have tremendous technological significance for practical application in industry. An understanding of the fundamental aspects and reaction mechanisms of the catalytic reactions reviewed in this study would support the design of industrial catalysts. CO 2 reforming of methane utilizes CO 2, which is often stored in large quantities, to convert as a reactant. Strategies to eliminate carbon deposition, which is the major problem associated with this reaction, are discussed. The oxidative coupling of methane directly produces ethylene in one reactor through a slightly exothermic reaction, potentially minimizing the capital cost of the natural gas conversion process. The focus of discussion in this review will be on the attainable yield of C 2 products by rigorous kinetic analyses.

  15. Fourth annual conference on materials for coal conversion and utilization

    Energy Technology Data Exchange (ETDEWEB)

    1979-01-01

    The fourth annual conference on materials for coal conversion and utilization was held October 9 to 11, 1979, at the National Bureau of Standards, Gaithersburg, Maryland. It was sponsored by the National Bureau of Standards, the Electric Power Research Institute, the US Department of Energy, and the Gas Research Institute. The papers have been entered individually into EDB and ERA. (LTN)

  16. Mathematical simulation of plasma-chemical coal conversion

    Energy Technology Data Exchange (ETDEWEB)

    Messerle, A.V. [Bauman State Technical University, Moscow (Russian Federation)

    2004-02-01

    A mathematical model that describes the conversion of a coal-dust flow in a cylindrical plasma reactor is presented. The model describes a two-phase (coal particles + air) chemically reacting flow, which propagates in a channel with or without an internal heat source (an electric arc, a plasmatron torch, or exothermic chemical reactions). The model is based on the assumption that the process is quasi-stationary and one-dimensional; coal particles are taken as isothermal, and ash is assumed to be an inert component. The model represents the composition of coals by their organic and mineral constituents. The model was implemented as a pro-ram for personal computers; calculations performed with the use of this program are in satisfactory agreement with experimental data.

  17. Measurement and modeling of advanced coal conversion processes

    Energy Technology Data Exchange (ETDEWEB)

    Solomon, P.R.; Serio, M.A.; Hamblen, D.G. (Advanced Fuel Research, Inc., East Hartford, CT (USA)); Smoot, L.D.; Brewster, B.S. (Brigham Young Univ., Provo, UT (USA))

    1990-01-01

    The overall objective of this program is the development of predictive capability for the design, scale up, simulation, control and feedstock evaluation in advanced coal conversion devices. This technology is important to reduce the technical and economic risks inherent in utilizing coal, a feedstock whose variable and often unexpected behavior presents a significant challenge. This program will merge significant advances made at Advanced Fuel Research, Inc. (AFR) in measuring and quantitatively describing the mechanisms in coal conversion behavior, with technology being developed at Brigham Young University (BYU) in comprehensive computer codes for mechanistic modeling of entrained-bed gasification. Additional capabilities in predicting pollutant formation will be implemented and the technology will be expanded to fixed-bed reactors. The foundation to describe coal-specific conversion behavior is AFR's Functional Group (FG) and Devolatilization, Vaporization, and Crosslinking (DVC) models, developed under previous and on-going METC sponsored programs. These models have demonstrated the capability to describe the time dependent evolution of individual gas species, and the amount and characteristics of tar and char. The combined FG-DVC model will be integrated with BYU's comprehensive two-dimensional reactor model, PCGC-2, which is currently the most widely used reactor simulation for combustion or gasification. Success in this program will be a major step in improving in predictive capabilities for coal conversion processes including: demonstrated accuracy and reliability and a generalized first principles'' treatment of coals based on readily obtained composition data. The progress during the fifteenth quarterly of the program is presented. 56 refs., 41 figs., 5 tabs.

  18. Proceedings of the third annual underground coal conversion symposium

    Energy Technology Data Exchange (ETDEWEB)

    None

    1977-01-01

    The Third Annual Underground Coal Conversion Symposium was held at Fallen Leaf Lake, CA, June 6--9, 1977. It was sponsored by the U.S. Department of Energy and hosted by Lawrence Livermore Laboratory. Forty-one papers have been entered individually into EDB and ERA; ten papers had been entered previously from other sources. The papers cover the in-situ gasification of lignite, subbituminous coal and bituminous coal, in flat lying seams and a steeply dipping beds, at moderate and at greater depths, and describe various technologies of (borehole linking, well spacings, gasifying agents (air, oxygen, steam, hydrogen, including mixtures). Measuring instruments for diagnostic and process control purposes are described. Environmental impacts (ground subsidence and possible groundwater pollution) are the subject of several papers. Finally, mathematical modelling and projected economics of the process are developed. (LTN)

  19. Proceedings of the 5th underground coal conversion symposium

    Energy Technology Data Exchange (ETDEWEB)

    None

    1979-05-01

    The 5th underground coal conversion symposium was held at Alexandria, Virginia, June 18--21, 1979. Thirty-three papers have been entered individually into EDB and ERA. Seven papers were also abstracted for Energy Abstracts for Policy Analysis. Seven papers had been entered previously from other sources. The symposium was sponsored by the US Department of Energy, Division of Fossil Fuel Extraction. (LTN)

  20. Coal conversion processes and their materials requirements. Physical sciences

    Energy Technology Data Exchange (ETDEWEB)

    Marriott, J.B.; Voorde, M. van de; Betteridge, W.

    1984-01-01

    The coal conversion processes combustion, gasification and liquefaction are discussed with respect to current industrial developments and material problems in industrial plants due to fouling, corrosion and erosion. The available materials are discussed by means of high temperature corrosion, erosion, ductibility, creep, fatigue and physical properties. Ceramics and refractories which are particularly used as thermal insulation are also discussed by means of corrosion and erosion and mechanical properties.

  1. Green technology for conversion of renewable hydrocarbon based on plasma-catalytic approach

    Science.gov (United States)

    Fedirchyk, Igor; Nedybaliuk, Oleg; Chernyak, Valeriy; Demchina, Valentina

    2016-09-01

    The ability to convert renewable biomass into fuels and chemicals is one of the most important steps on our path to green technology and sustainable development. However, the complex composition of biomass poses a major problem for established conversion technologies. The high temperature of thermochemical biomass conversion often leads to the appearance of undesirable byproducts and waste. The catalytic conversion has reduced yield and feedstock range. Plasma-catalytic reforming technology opens a new path for biomass conversion by replacing feedstock-specific catalysts with free radicals generated in the plasma. We studied the plasma-catalytic conversion of several renewable hydrocarbons using the air plasma created by rotating gliding discharge. We found that plasma-catalytic hydrocarbon conversion can be conducted at significantly lower temperatures (500 K) than during the thermochemical ( 1000 K) and catalytic (800 K) conversion. By using gas chromatography, we determined conversion products and found that conversion efficiency of plasma-catalytic conversion reaches over 85%. We used obtained data to determine the energy yield of hydrogen in case of plasma-catalytic reforming of ethanol and compared it with other plasma-based hydrogen-generating systems.

  2. COST OF SELECTIVE CATALYTIC REDUCTION (SCR) APPLICATION FOR NOX CONTROL ON COAL-FIRED BOILERS

    Science.gov (United States)

    The report provides a methodology for estimating budgetary costs associated with retrofit applications of selective catalytic reduction (SCR) technology on coal-fired boilers. SCR is a postcombustion nitrogen oxides (NOx) control technology capable of providing NOx reductions >90...

  3. Catalytic conversion of nonfood woody biomass solids to organic liquids.

    Science.gov (United States)

    Barta, Katalin; Ford, Peter C

    2014-05-20

    This Account outlines recent efforts in our laboratories addressing a fundamental challenge of sustainability chemistry, the effective utilization of biomass for production of chemicals and fuels. Efficient methods for converting renewable biomass solids to chemicals and liquid fuels would reduce society's dependence on nonrenewable petroleum resources while easing the atmospheric carbon dioxide burden. The major nonfood component of biomass is lignocellulose, a matrix of the biopolymers cellulose, hemicellulose, and lignin. New approaches are needed to effect facile conversion of lignocellulose solids to liquid fuels and to other chemical precursors without the formation of intractable side products and with sufficient specificity to give economically sustainable product streams. We have devised a novel catalytic system whereby the renewable feedstocks cellulose, organosolv lignin, and even lignocellulose composites such as sawdust are transformed into organic liquids. The reaction medium is supercritical methanol (sc-MeOH), while the catalyst is a copper-doped porous metal oxide (PMO) prepared from inexpensive, Earth-abundant starting materials. This transformation occurs in a single stage reactor operating at 300-320 °C and 160-220 bar. The reducing equivalents for these transformations are derived by the reforming of MeOH (to H2 and CO), which thereby serves as a "liquid syngas" in the present case. Water generated by deoxygenation processes is quickly removed by the water-gas shift reaction. The Cu-doped PMO serves multiple purposes, catalyzing substrate hydrogenolysis and hydrogenation as well as the methanol reforming and shift reactions. This one-pot "UCSB process" is quantitative, giving little or no biochar residual. Provided is an overview of these catalysis studies beginning with reactions of the model compound dihydrobenzofuran that help define the key processes occurring. The initial step is phenyl-ether bond hydrogenolysis, and this is followed by

  4. Future economic conversion of coal to electricity. Zukuenftige wirtschaftliche Kohleverstromung

    Energy Technology Data Exchange (ETDEWEB)

    Kotschenreuther, H.; Haeuser, U.; Weirich, P.H. (Asea Brown Boveri AG, Mannheim (Germany). Geschaeftsbereich Kraftwerke)

    1993-01-01

    Available and exhaustible development potential is essential for making a decision on the choice of a new power plant technology. The criteria for potential development will be increase in efficiency in the whole load range with constant or improved economics, operating performance compatible with today's requirements and possibilities of application in the intermediate or upper medium-load range. The power plant concepts which promise success from today's point of view for the conversion of bituminous coal to electricity are indicated. (orig.).

  5. Economic conversion of coal into electricity in the future

    Energy Technology Data Exchange (ETDEWEB)

    Kotschenreuther, H.; Haeuser, U.; Weirich, P.-H. (ABB Kraftwerke AG, Mannheim (Germany))

    1993-01-01

    Available and exhaustible development potential is essential for making a decision on the choice of a new power plant technology. The criteria for potential development will be increased in efficiency in the whole load range with constant or improved economics, operating performance compatible with today's requirements and possibilities of application in the intermediate or upper medium-load range.The power plant concepts which promise success from today's point of view for the conversion of bituminous coal to electricity are indicated. These include the high-temperature steam power plant. 17 figs., 1 tab.

  6. Integrated Biomass Gasification with Catalytic Partial Oxidation for Selective Tar Conversion

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Lingzhi; Wei, Wei; Manke, Jeff; Vazquez, Arturo; Thompson, Jeff; Thompson, Mark

    2011-05-28

    Biomass gasification is a flexible and efficient way of utilizing widely available domestic renewable resources. Syngas from biomass has the potential for biofuels production, which will enhance energy security and environmental benefits. Additionally, with the successful development of low Btu fuel engines (e.g. GE Jenbacher engines), syngas from biomass can be efficiently used for power/heat co-generation. However, biomass gasification has not been widely commercialized because of a number of technical/economic issues related to gasifier design and syngas cleanup. Biomass gasification, due to its scale limitation, cannot afford to use pure oxygen as the gasification agent that used in coal gasification. Because, it uses air instead of oxygen, the biomass gasification temperature is much lower than well-understood coal gasification. The low temperature leads to a lot of tar formation and the tar can gum up the downstream equipment. Thus, the biomass gasification tar removal is a critical technology challenge for all types of biomass gasifiers. This USDA/DOE funded program (award number: DE-FG36-O8GO18085) aims to develop an advanced catalytic tar conversion system that can economically and efficiently convert tar into useful light gases (such as syngas) for downstream fuel synthesis or power generation. This program has been executed by GE Global Research in Irvine, CA, in collaboration with Professor Lanny Schmidt's group at the University of Minnesota (UoMn). Biomass gasification produces a raw syngas stream containing H2, CO, CO2, H2O, CH4 and other hydrocarbons, tars, char, and ash. Tars are defined as organic compounds that are condensable at room temperature and are assumed to be largely aromatic. Downstream units in biomass gasification such as gas engine, turbine or fuel synthesis reactors require stringent control in syngas quality, especially tar content to avoid plugging (gum) of downstream equipment. Tar- and ash-free syngas streams are a critical

  7. Proximate analysis of coal and solid products from coal conversion by thermogravimetric analysis

    Energy Technology Data Exchange (ETDEWEB)

    Iacchelli, A.; Selucky, M.

    1983-01-01

    Proximate analysis of coals consists of the determination of moisture, volatile matter, ash and fixed carbon in a sample. This report shows that this analysis can be accomplished using thermal gravimetric analysis (TGA) as a procedure which can simulate all conditions involved. The influence of various variables, such as sample size, purge gas flow rate, temperature program and coal rank have been studied using coal samples ranging in rank from low volatile bituminous coals to lignites. The TGA procedure practically eliminates sample contact with ambient air and reduces sample handling to detemining (automatically) its original weight before the start of the analysis. The whole proximate analysis is essentially a one-step procedure. The use of oxygen after volatile matter removal allows direct burning of fixed carbon as a direct determination of its weight. The method is fast and well repeatable and is recommended as a semiroutine procedure, especially for very small samples from minibomb experiments, or where additional information on the course of sample devolatilization is of interest, such as in the analysis of pyridine and toluene extracts and the various insoluble materials form coal conversion experiments. 7 refs., 13 figs., 4 tabs.

  8. An Integrated System for the Treatment of Coal Conversion Wastewater

    Energy Technology Data Exchange (ETDEWEB)

    Henry Y. Wang; Keeran R. Srinivasan

    1999-02-25

    Treatment of mixed waste from coal conversion wastewaters involves the degradation of toxic organics and the removal of heavy metals. An integrated and cost-effective treatment scheme that can implement such a process is considered essential to promote continued development and growth of coal conversion processes without any deleterious effects on our ecosystem. We have recently developed a pH-dependent, reversible heavy metal adsorption/desorption process which promises to be a cost-effective alternative to the treatment and disposal options currently in place for these inorganic contaminants. Our work shows that: (1) Polydisperse, industrial-grade surfactants can be used in the development of novel, surfactant-coated smectitic clays containing up to 50% by weight of adsorbed surfactant, (2) Reversible adsorption and resorption of cationic (CU(II) and Cd(II)) and anionic (Cr(VI)) heavy metals from their respective aqueous solutions onto these surfactant-modified smectites can be effected using pH of the medium as a switch, and (3) These surfactant-modified smectites can be repeatedly used (up to 5 times) with only a minimal loss in their adsorption potency and with very little leaching of the adsorbed surfactants.

  9. Survey of industrial coal conversion equipment capabilities: valves

    Energy Technology Data Exchange (ETDEWEB)

    Bush, W. A.; Slade, E. C.

    1978-06-01

    A survey of the industrial capabilities of the valve and valve-actuator industry to supply large, high-pressure stop valves for the future coal conversion industry is presented in this report. Also discussed are development and testing capabilities of valve and valve-actuator manufacturers and anticipated lead times required to manufacture advanced design valves for the most stringent service applications. Results indicate that the valve and valve-actuator industry is capable of manufacturing in quantity equipment of the size and for the pressure and temperature ranges which would be required in the coal conversion industry. Valve manufacturers do not, however, have sufficient product application experience to predict the continuing functional ability of valves used for lock-hopper feeders, slurry feeders, and slag-char letdown service. Developmental and testing efforts to modify existing valve designs or to develop new valve concepts for these applications were estimated to range from 1 to 6 years. A testing facility to simulate actuation of critical valves under service conditions would be beneficial.

  10. Catalytic properties of raw and modified semicokes from Kansk-Achinsk coals

    Energy Technology Data Exchange (ETDEWEB)

    Stavitskaya, S.S.; Tarkovskaya, I.A.; Nikolaeva, V.A.; Goba, V.E.

    1984-03-01

    Power of semicokes prepared from coals to accelerate several protolytic and oxidation-reduction reactions is studied. By special treatment of Kansk-Achinsk coals it is possible to regulate the surface properties and produce an inexpensive coal catalyst for dechlorination of brine, liquid phase esterification, breakdown of heavy water, etc. The catalytic properties of the modified semicokes are close to those of widely used activated and oxidized coals. Testing was performed on raw semicoke, semicoke processed at different temperatures, air oxidized semicoke, nitrogen oxidized and semicoke subjected to various conditions of oxidation-reduction reactions and their several forms of cation exchange. 10 references.

  11. Conceptual flow sheets development for coal conversion plant coal handling-preparation and ash/slag removal operations

    Energy Technology Data Exchange (ETDEWEB)

    1979-07-01

    This report presents 14 conceptual flow sheets and major equipment lists for coal handling and preparation operations that could be required for future, commercial coal conversion plants. These flow sheets are based on converting 50,000 tons per day of clean coal representative of the Pittsburgh and Kentucky No. 9 coal seams. Flow sheets were used by Union Carbide Corporation, Oak Ridge National Laboratory, in a survey of coal handling/preparation equipment requirements for future coal conversion plants. Operations covered in this report include run-of-mine coal breaking, coarse coal cleaning, fine coal cleaning, live storage and blending, fine crushing (crushing to top sizes ranging from 1/4-inch to 20 mesh), drying, and grinding (70 percent minus 200 mesh). Two conceptual flow sheets and major equipment lists are also presented for handling ash or granulated slag and other solid wastes produced by nine leading coal conversion processes. These flow sheets provide for solid wastes transport to an environmentally acceptable disposal site as either dry solids or as a water slurry.

  12. Catalytic multi-stage liquefaction of coal at HTI: Bench-scale studies in coal/waste plastics coprocessing

    Energy Technology Data Exchange (ETDEWEB)

    Pradhan, V.R.; Lee, L.K.; Stalzer, R.H. [Hydrocarbon Technologies, Inc., Lawrenceville, NJ (United States)] [and others

    1995-12-31

    The development of Catalytic Multi-Stage Liquefaction (CMSL) at HTI has focused on both bituminous and sub-bituminous coals using laboratory, bench and PDU scale operations. The crude oil equivalent cost of liquid fuels from coal has been curtailed to about $30 per barrel, thus achieving over 30% reduction in the price that was evaluated for the liquefaction technologies demonstrated in the late seventies and early eighties. Contrary to the common belief, the new generation of catalytic multistage coal liquefaction process is environmentally very benign and can produce clean, premium distillates with a very low (<10ppm) heteroatoms content. The HTI Staff has been involved over the years in process development and has made significant improvements in the CMSL processing of coals. A 24 month program (extended to September 30, 1995) to study novel concepts, using a continuous bench scale Catalytic Multi-Stage unit (30kg coal/day), has been initiated since December, 1992. This program consists of ten bench-scale operations supported by Laboratory Studies, Modelling, Process Simulation and Economic Assessments. The Catalytic Multi-Stage Liquefaction is a continuation of the second generation yields using a low/high temperature approach. This paper covers work performed between October 1994- August 1995, especially results obtained from the microautoclave support activities and the bench-scale operations for runs CMSL-08 and CMSL-09, during which, coal and the plastic components for municipal solid wastes (MSW) such as high density polyethylene (HDPE)m, polypropylene (PP), polystyrene (PS), and polythylene terphthlate (PET) were coprocessed.

  13. Conversion of Hydrogen Sulfide in Coal Gases to Liquid Elemental Sulfur with Monolithic Catalysts

    Energy Technology Data Exchange (ETDEWEB)

    K. C. Kwon

    2006-09-30

    CO components of syngas appear to behave as inert with respect to sulfur formed at the SSRP conditions. One problem in the SSRP process that needs to be eliminated or minimized is COS formation that may occur due to reaction of CO with sulfur formed from the Claus reaction. The objectives of this research are to formulate monolithic catalysts for removal of H{sub 2}S from coal gases and minimum formation of COS with monolithic catalyst supports, {gamma}-alumina wash or carbon coats, and catalytic metals, to develop a catalytic regeneration method for a deactivated monolithic catalyst, to measure kinetics of both direct oxidation of H{sub 2}S to elemental sulfur with SO{sub 2} as an oxidizer and formation of COS in the presence of a simulated coal gas mixture containing H{sub 2}, CO, CO{sub 2}, and moisture, using a monolithic catalyst reactor, and to develop kinetic rate equations and model the direct oxidation process to assist in the design of large-scale plants. This heterogeneous catalytic reaction has gaseous reactants such as H{sub 2}S and SO{sub 2}. However, this heterogeneous catalytic reaction has heterogeneous products such as liquid elemental sulfur and steam. To achieve the above-mentioned objectives using a monolithic catalyst reactor, experiments on conversion of hydrogen sulfide into elemental sulfur and formation of COS were carried out for the space time range of 40-560 seconds at 120-150 C to evaluate effects of reaction temperatures, total pressure, space time, and catalyst regeneration on conversion of hydrogen sulfide into elemental sulfur and formation of COS. Simulated coal gas mixtures consist of 3,600-4,000-ppmv hydrogen sulfide, 1,800-2,000 ppmv sulfur dioxide, 23-27 v% hydrogen, 36-41 v% CO, 10-12 v% CO{sub 2}, 0-10 vol % moisture, and nitrogen as remainder. Volumetric feed rates of a simulated coal gas mixture to the reactor are 30-180 SCCM. The temperature of the reactor is controlled in an oven at 120-150 C. The pressure of the reactor

  14. Conversion of Hydrogen Sulfide in Coal Gases to Liquid Elemental Sulfur with Monolithic Catalysts

    Energy Technology Data Exchange (ETDEWEB)

    K. C. Kwon

    2006-09-30

    CO components of syngas appear to behave as inert with respect to sulfur formed at the SSRP conditions. One problem in the SSRP process that needs to be eliminated or minimized is COS formation that may occur due to reaction of CO with sulfur formed from the Claus reaction. The objectives of this research are to formulate monolithic catalysts for removal of H{sub 2}S from coal gases and minimum formation of COS with monolithic catalyst supports, {gamma}-alumina wash or carbon coats, and catalytic metals, to develop a catalytic regeneration method for a deactivated monolithic catalyst, to measure kinetics of both direct oxidation of H{sub 2}S to elemental sulfur with SO{sub 2} as an oxidizer and formation of COS in the presence of a simulated coal gas mixture containing H{sub 2}, CO, CO{sub 2}, and moisture, using a monolithic catalyst reactor, and to develop kinetic rate equations and model the direct oxidation process to assist in the design of large-scale plants. This heterogeneous catalytic reaction has gaseous reactants such as H{sub 2}S and SO{sub 2}. However, this heterogeneous catalytic reaction has heterogeneous products such as liquid elemental sulfur and steam. To achieve the above-mentioned objectives using a monolithic catalyst reactor, experiments on conversion of hydrogen sulfide into elemental sulfur and formation of COS were carried out for the space time range of 40-560 seconds at 120-150 C to evaluate effects of reaction temperatures, total pressure, space time, and catalyst regeneration on conversion of hydrogen sulfide into elemental sulfur and formation of COS. Simulated coal gas mixtures consist of 3,600-4,000-ppmv hydrogen sulfide, 1,800-2,000 ppmv sulfur dioxide, 23-27 v% hydrogen, 36-41 v% CO, 10-12 v% CO{sub 2}, 0-10 vol % moisture, and nitrogen as remainder. Volumetric feed rates of a simulated coal gas mixture to the reactor are 30-180 SCCM. The temperature of the reactor is controlled in an oven at 120-150 C. The pressure of the reactor

  15. Conversion of Hydrogen Sulfide in Coal Gases to Liquid Elemental Sulfur with Monolithic Catalysts

    Energy Technology Data Exchange (ETDEWEB)

    K. C. Kwon

    2007-09-30

    CO components of syngas appear to behave as inert with respect to sulfur formed at the SSRP conditions. One problem in the SSRP process that needs to be eliminated or minimized is COS formation that may occur due to reaction of CO with sulfur formed from the Claus reaction. The objectives of this research are to formulate monolithic catalysts for removal of H{sub 2}S from coal gases and minimum formation of COS with monolithic catalyst supports, {gamma}-alumina wash or carbon coats, and catalytic metals, to develop a catalytic regeneration method for a deactivated monolithic catalyst, to measure kinetics of both direct oxidation of H{sub 2}S to elemental sulfur with SO{sub 2} as an oxidizer and formation of COS in the presence of a simulated coal gas mixture containing H{sub 2}, CO, CO{sub 2}, and moisture, using a monolithic catalyst reactor, and to develop kinetic rate equations and model the direct oxidation process to assist in the design of large-scale plants. This heterogeneous catalytic reaction has gaseous reactants such as H{sub 2}S and SO{sub 2}. However, this heterogeneous catalytic reaction has heterogeneous products such as liquid elemental sulfur and steam. Experiments on conversion of hydrogen sulfide into elemental sulfur and formation of COS were carried out for the space time range of 130-156 seconds at 120-140 C to formulate catalysts suitable for the removal of H{sub 2}S and COS from coal gases, evaluate removal capabilities of hydrogen sulfide and COS from coal gases with formulated catalysts, and develop an economic regeneration method of deactivated catalysts. Simulated coal gas mixtures consist of 3,300-3,800-ppmv hydrogen sulfide, 1,600-1,900 ppmv sulfur dioxide, 18-21 v% hydrogen, 29-34 v% CO, 8-10 v% CO{sub 2}, 5-18 vol % moisture, and nitrogen as remainder. Volumetric feed rates of a simulated coal gas mixture to the reactor are 114-132 SCCM. The temperature of the reactor is controlled in an oven at 120-140 C. The pressure of the reactor

  16. Conversion of Hydrogen Sulfide in Coal Gases to Liquid Elemental Sulfur with Monolithic Catalysts

    Energy Technology Data Exchange (ETDEWEB)

    K. C. Kwon

    2007-09-30

    CO components of syngas appear to behave as inert with respect to sulfur formed at the SSRP conditions. One problem in the SSRP process that needs to be eliminated or minimized is COS formation that may occur due to reaction of CO with sulfur formed from the Claus reaction. The objectives of this research are to formulate monolithic catalysts for removal of H{sub 2}S from coal gases and minimum formation of COS with monolithic catalyst supports, {gamma}-alumina wash or carbon coats, and catalytic metals, to develop a catalytic regeneration method for a deactivated monolithic catalyst, to measure kinetics of both direct oxidation of H{sub 2}S to elemental sulfur with SO{sub 2} as an oxidizer and formation of COS in the presence of a simulated coal gas mixture containing H{sub 2}, CO, CO{sub 2}, and moisture, using a monolithic catalyst reactor, and to develop kinetic rate equations and model the direct oxidation process to assist in the design of large-scale plants. This heterogeneous catalytic reaction has gaseous reactants such as H{sub 2}S and SO{sub 2}. However, this heterogeneous catalytic reaction has heterogeneous products such as liquid elemental sulfur and steam. Experiments on conversion of hydrogen sulfide into elemental sulfur and formation of COS were carried out for the space time range of 130-156 seconds at 120-140 C to formulate catalysts suitable for the removal of H{sub 2}S and COS from coal gases, evaluate removal capabilities of hydrogen sulfide and COS from coal gases with formulated catalysts, and develop an economic regeneration method of deactivated catalysts. Simulated coal gas mixtures consist of 3,300-3,800-ppmv hydrogen sulfide, 1,600-1,900 ppmv sulfur dioxide, 18-21 v% hydrogen, 29-34 v% CO, 8-10 v% CO{sub 2}, 5-18 vol % moisture, and nitrogen as remainder. Volumetric feed rates of a simulated coal gas mixture to the reactor are 114-132 SCCM. The temperature of the reactor is controlled in an oven at 120-140 C. The pressure of the reactor

  17. Integrated Biomass Gasification with Catalytic Partial Oxidation for Selective Tar Conversion

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Lingzhi; Wei, Wei; Manke, Jeff; Vazquez, Arturo; Thompson, Jeff; Thompson, Mark

    2011-05-28

    Biomass gasification is a flexible and efficient way of utilizing widely available domestic renewable resources. Syngas from biomass has the potential for biofuels production, which will enhance energy security and environmental benefits. Additionally, with the successful development of low Btu fuel engines (e.g. GE Jenbacher engines), syngas from biomass can be efficiently used for power/heat co-generation. However, biomass gasification has not been widely commercialized because of a number of technical/economic issues related to gasifier design and syngas cleanup. Biomass gasification, due to its scale limitation, cannot afford to use pure oxygen as the gasification agent that used in coal gasification. Because, it uses air instead of oxygen, the biomass gasification temperature is much lower than well-understood coal gasification. The low temperature leads to a lot of tar formation and the tar can gum up the downstream equipment. Thus, the biomass gasification tar removal is a critical technology challenge for all types of biomass gasifiers. This USDA/DOE funded program (award number: DE-FG36-O8GO18085) aims to develop an advanced catalytic tar conversion system that can economically and efficiently convert tar into useful light gases (such as syngas) for downstream fuel synthesis or power generation. This program has been executed by GE Global Research in Irvine, CA, in collaboration with Professor Lanny Schmidt's group at the University of Minnesota (UoMn). Biomass gasification produces a raw syngas stream containing H2, CO, CO2, H2O, CH4 and other hydrocarbons, tars, char, and ash. Tars are defined as organic compounds that are condensable at room temperature and are assumed to be largely aromatic. Downstream units in biomass gasification such as gas engine, turbine or fuel synthesis reactors require stringent control in syngas quality, especially tar content to avoid plugging (gum) of downstream equipment. Tar- and ash-free syngas streams are a critical

  18. Catalytic properties of initial and modified semicokes from Kansk-Achinsk coals

    Energy Technology Data Exchange (ETDEWEB)

    Stavitskaya, S.S.; Tarkovskaya, I.A.; Nikolaeva, V.A.; Goba, V.E.

    1984-01-01

    Special treatment of coals, especially those used for the production of activated carbon, can be used to regulate selected properties of their surface and at the same time produce high-activity, low-cost carbon catalysts. The close similarity between the catalytic properties of the modified semi-cokes and oxidised and activated carbons suggests that it should be possible to use Kansk-Achinsk coals to produce effective industrial catalysts.

  19. Enhanced Heterogeneous Catalytic Conversion of Furfuryl Alcohol into Butyl Levulinate

    NARCIS (Netherlands)

    Carà, P.D..; Ciriminna, R.; Shiju, N.R.; Rothenberg, G.; Pagliaro, M.

    2014-01-01

    We study the catalytic condensation of furfuryl alcohol with 1-butanol to butyl levulinate. A screening of several commercial and as-synthesized solid acid catalysts shows that propylsulfonic acid-functionalized mesoporous silica outperforms the state-of-the-art phosphotungstate acid catalysts. The

  20. Conversion of Hydrogen Sulfide in Coal Gases to Liquid Elemental Sulfur with Monolithic Catalysts

    Energy Technology Data Exchange (ETDEWEB)

    K.C. Kwon

    2009-09-30

    CO components of syngas appear to behave as inert with respect to sulfur formed at the SSRP conditions. One problem in the SSRP process that needs to be eliminated or minimized is COS formation that may occur due to reaction of CO with sulfur formed from the Claus reaction. The objectives of this research are to formulate monolithic catalysts for removal of H{sub 2}S from coal gases and minimum formation of COS with monolithic catalyst supports, {gamma}-alumina wash coat, and catalytic metals, to develop a regeneration method for a deactivated monolithic catalyst, to measure kinetics of both direct oxidation of H{sub 2}S to elemental sulfur with SO{sub 2} as an oxidizer and formation of COS in the presence of a simulated coal gas mixture containing H{sub 2}, CO, CO{sub 2}, and moisture, using a monolithic catalyst reactor. The task of developing kinetic rate equations and modeling the direct oxidation process to assist in the design of large-scale plants will be abandoned since formulation of catalysts suitable for the removal of H{sub 2}S and COS is being in progress. This heterogeneous catalytic reaction has gaseous reactants such as H{sub 2}S and SO{sub 2}. However, this heterogeneous catalytic reaction has heterogeneous products such as liquid elemental sulfur and steam. Experiments on conversion of hydrogen sulfide into elemental sulfur and formation of COS were carried out for the space time range of 46-570 seconds under reaction conditions to formulate catalysts suitable for the removal of H{sub 2}S and COS from coal gases and evaluate their capabilities in reducing hydrogen sulfide and COS in coal gases. Simulated coal gas mixtures consist of 3,200-4,000-ppmv hydrogen sulfide, 1,600-20,000-ppmv sulfur dioxide, 18-27 v% hydrogen, 29-41 v% CO, 8-12 v% CO{sub 2}, 0-10 vol % moisture, and nitrogen as remainder. Volumetric feed rates of simulated coal gas mixtures to the reactor are 30 - 180 cm{sup 3}/min at 1 atm and 25 C (SCCM). The temperature of the reactor is

  1. Conversion of Hydrogen Sulfide in Coal Gases to Liquid Elemental Sulfur with Monolithic Catalysts

    Energy Technology Data Exchange (ETDEWEB)

    K.C. Kwon

    2009-09-30

    CO components of syngas appear to behave as inert with respect to sulfur formed at the SSRP conditions. One problem in the SSRP process that needs to be eliminated or minimized is COS formation that may occur due to reaction of CO with sulfur formed from the Claus reaction. The objectives of this research are to formulate monolithic catalysts for removal of H{sub 2}S from coal gases and minimum formation of COS with monolithic catalyst supports, {gamma}-alumina wash coat, and catalytic metals, to develop a regeneration method for a deactivated monolithic catalyst, to measure kinetics of both direct oxidation of H{sub 2}S to elemental sulfur with SO{sub 2} as an oxidizer and formation of COS in the presence of a simulated coal gas mixture containing H{sub 2}, CO, CO{sub 2}, and moisture, using a monolithic catalyst reactor. The task of developing kinetic rate equations and modeling the direct oxidation process to assist in the design of large-scale plants will be abandoned since formulation of catalysts suitable for the removal of H{sub 2}S and COS is being in progress. This heterogeneous catalytic reaction has gaseous reactants such as H{sub 2}S and SO{sub 2}. However, this heterogeneous catalytic reaction has heterogeneous products such as liquid elemental sulfur and steam. Experiments on conversion of hydrogen sulfide into elemental sulfur and formation of COS were carried out for the space time range of 46-570 seconds under reaction conditions to formulate catalysts suitable for the removal of H{sub 2}S and COS from coal gases and evaluate their capabilities in reducing hydrogen sulfide and COS in coal gases. Simulated coal gas mixtures consist of 3,200-4,000-ppmv hydrogen sulfide, 1,600-20,000-ppmv sulfur dioxide, 18-27 v% hydrogen, 29-41 v% CO, 8-12 v% CO{sub 2}, 0-10 vol % moisture, and nitrogen as remainder. Volumetric feed rates of simulated coal gas mixtures to the reactor are 30 - 180 cm{sup 3}/min at 1 atm and 25 C (SCCM). The temperature of the reactor is

  2. Experimental Investigation of Flow Resistance in a Coal Mine Ventilation Air Methane Preheated Catalytic Oxidation Reactor

    Directory of Open Access Journals (Sweden)

    Bin Zheng

    2015-01-01

    Full Text Available This paper reports the results of experimental investigation of flow resistance in a coal mine ventilation air methane preheated catalytic oxidation reactor. The experimental system was installed at the Energy Research Institute of Shandong University of Technology. The system has been used to investigate the effects of flow rate (200 Nm3/h to 1000 Nm3/h and catalytic oxidation bed average temperature (20°C to 560°C within the preheated catalytic oxidation reactor. The pressure drop and resistance proportion of catalytic oxidation bed, the heat exchanger preheating section, and the heat exchanger flue gas section were measured. In addition, based on a large number of experimental data, the empirical equations of flow resistance are obtained by the least square method. It can also be used in deriving much needed data for preheated catalytic oxidation designs when employed in industry.

  3. Catalytic conversion of alcohols to hydrocarbons with low benzene content

    Energy Technology Data Exchange (ETDEWEB)

    Narula, Chaitanya K.; Davison, Brian H.; Keller, Martin

    2016-09-06

    A method for converting an alcohol to a hydrocarbon fraction having a lowered benzene content, the method comprising: converting said alcohol to a hydrocarbon fraction by contacting said alcohol, under conditions suitable for converting said alcohol to said hydrocarbon fraction, with a metal-loaded zeolite catalyst catalytically active for converting said alcohol to said hydrocarbon fraction, and contacting said hydrocarbon fraction with a benzene alkylation catalyst, under conditions suitable for alkylating benzene, to form alkylated benzene product in said hydrocarbon fraction. Also described is a catalyst composition useful in the method, comprising a mixture of (i) a metal-loaded zeolite catalyst catalytically active for converting said alcohol to said hydrocarbon, and (ii) a benzene alkylation catalyst, in which (i) and (ii) may be in a mixed or separated state. A reactor for housing the catalyst and conducting the reaction is also described.

  4. Catalytic conversion of alcohols to hydrocarbons with low benzene content

    Energy Technology Data Exchange (ETDEWEB)

    Narula, Chaitanya K.; Davison, Brian H.; Keller, Martin

    2016-03-08

    A method for converting an alcohol to a hydrocarbon fraction having a lowered benzene content, the method comprising: converting said alcohol to a hydrocarbon fraction by contacting said alcohol, under conditions suitable for converting said alcohol to said hydrocarbon fraction, with a metal-loaded zeolite catalyst catalytically active for converting said alcohol to said hydrocarbon fraction, and contacting said hydrocarbon fraction with a benzene alkylation catalyst, under conditions suitable for alkylating benzene, to form alkylated benzene product in said hydrocarbon fraction. Also described is a catalyst composition useful in the method, comprising a mixture of (i) a metal-loaded zeolite catalyst catalytically active for converting said alcohol to said hydrocarbon, and (ii) a benzene alkylation catalyst, in which (i) and (ii) may be in a mixed or separated state. A reactor for housing the catalyst and conducting the reaction is also described.

  5. PARAMETRIC EVALUATION OF VOC CONVERSION VIA CATALYTIC INCINERATION

    Directory of Open Access Journals (Sweden)

    Kaskantzis Neto G.

    1997-01-01

    Full Text Available Abstract - A pilot-scale catalytic incineration system was used to investigate the effectiveness of catalytic incineration as a means of reducing volatile organic compound (VOC air pollutants. The objectives of the study were: 1 to investigate the effects of operating and design variables on the reduction efficiency of VOCs; and 2 to evaluate reduction efficiencies for specific compounds in different chemical classes. The study results verified that the following factors affect the catalyst performance: inlet temperature, space velocity, compound type, and compound inlet concentration. Tests showed that reduction efficiencies exceeding 98% were possible, given sufficiently high inlet gas temperatures for the following classes of compounds: alcohols, acetates, ketones, hydrocarbons, and aromatics

  6. Multiscale-tailored bioelectrode surfaces for optimized catalytic conversion efficiency.

    Science.gov (United States)

    Bon Saint Côme, Yémima; Lalo, Hélène; Wang, Zhijie; Etienne, Mathieu; Gajdzik, Janine; Kohring, Gert-Wieland; Walcarius, Alain; Hempelmann, Rolf; Kuhn, Alexander

    2011-10-18

    We describe the elaboration of a multiscale-tailored bioelectrocatalytic system. The combination of two enzymes, D-sorbitol dehydrogenase and diaphorase, is studied with respect to the oxidation of D-sorbitol as a model system. The biomolecules are immobilized in an electrodeposited paint (EDP) layer. Reproducible and efficient catalysis of D-sorbitol oxidation is recorded when this system is immobilized on a gold electrode modified by a self-assembled monolayer of 4-carboxy-(2,5,7-trinitro-9-fluorenylidene)malonitrile used as a mediator. The insertion of mediator-modified gold nanoparticles into the EDP film increases significantly the active surface area for the catalytic reaction, which can be further enhanced when the whole system is immobilized in macroporous gold electrodes. This multiscale architecture finally leads to a catalytic device with optimized efficiency for potential use in biosensors, bioelectrosynthesis, and biofuel cells.

  7. Fabrication of bimetallic nanostructures via aerosol-assisted electroless silver deposition for catalytic CO conversion.

    Science.gov (United States)

    Byeon, Jeong Hoon; Kim, Jang-Woo

    2014-03-12

    Bimetallic nanostructures were fabricated via aerosol-assisted electroless silver deposition for catalytic CO conversion. An ambient spark discharge was employed to produce nanocatalysts, and the particles were directly deposited on a polytetrafluoroethylene substrate for initiating silver deposition to form Pd-Ag, Pt-Ag, Au-Ag bimetallic nanostructures as well as a pure Ag nanostructure. Kinetics and morphological evolutions in the silver deposition with different nanocatalysts were comparatively studied. The Pt catalyst displayed the highest catalytic activity for electroless silver deposition, followed by the order Pd > Au > Ag. Another catalytic activity of the fabricated bimetallic structures in the carbon monoxide conversion was further evaluated at low-temperature conditions. The bimetallic systems showed significantly higher catalytic activity than that from a pure Ag system.

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

    Energy Technology Data Exchange (ETDEWEB)

    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.

  9. Catalytic conversion of methanol to low molecular weight hydrocarbons. [Dissertation

    Energy Technology Data Exchange (ETDEWEB)

    Singh, B.B.

    1979-12-01

    The recent demands on the available energy have stimulated the search for alternatives to oil. Methanol, because of its abundance and the availability of technology to produce it from coal, is projected as an alternative source for producing low molecular weight olefins. Utilizing chabazite ion exchanged with ammonium and rare earth chlorides, methanol is converted to ethylene, propylene and propane with carbon yields of 70 to 90% at reaction temperatures of 633 to 723/sup 0/K and pressures from 1 to 18 atmospheres. X-ray diffraction studies, using Cu-K radiation, show no permanent structural changes after a long use. No permanent deactivation was observed even though the catalyst was overheated once, and have been deactivated and regenerated as many as 21 times. The ammonium exchange coupled with the water at high temperature suggest the formation of an ultrastable zeolite. Ethylene yields increase as the temperature increases from 633/sup 0/K to 723/sup 0/K.

  10. Design of generic coal conversion facilities: Indirect coal liquefaction, Fischer-Tropsch synthesis

    Energy Technology Data Exchange (ETDEWEB)

    1991-10-01

    A comprehensive review of Fischer-Tropsch (F-T) technology, including fixed, fluidized, and bubble column reactors, was undertaken in order to develop an information base before initiating the design of the Fischer-Tropsch indirect liquefaction PDU as a part of the Generic Coal Conversion Facilities to be built at the Pittsburgh Energy Technology Center (PETC). The pilot plant will include a fixed bed and slurry bubble column reactor for the F-T mode of operation. The review encompasses current status of both these technologies, their key variables, catalyst development, future directions, and potential improvement areas. However, more emphasis has been placed on the slurry bubble column reactor since this route is likely to be the preferred technology for commercialization, offering process advantages and, therefore, better economics than fixed and fluidized bed approaches.

  11. Energy Conversion Alternatives Study (ECAS), General Electric Phase 1. Volume 1: Executive summary. [using coal or coal derived fuels

    Science.gov (United States)

    Corman, J. C.

    1976-01-01

    A data base for the comparison of advanced energy conversion systems for utility applications using coal or coal-derived fuels was developed. Estimates of power plant performance (efficiency), capital cost, cost of electricity, natural resource requirements, and environmental intrusion characteristics were made for ten advanced conversion systems. Emphasis was on the energy conversion system in the context of a base loaded utility power plant. All power plant concepts were premised on meeting emission standard requirements. A steam power plant (3500 psig, 1000 F) with a conventional coal-burning furnace-boiler was analyzed as a basis for comparison. Combined cycle gas/steam turbine system results indicated competitive efficiency and a lower cost of electricity compared to the reference steam plant. The Open-Cycle MHD system results indicated the potential for significantly higher efficiency than the reference steam plant but with a higher cost of electricity.

  12. Mesoporous zeolite single crystals for catalytic hydrocarbon conversion

    DEFF Research Database (Denmark)

    Schmidt, I.; Christensen, C.H.; Hasselriis, Peter

    2005-01-01

    Recently, mesoporous zeolite single crystals were discovered. They constitute a novel family of materials that features a combined micropore and mesopore architecture within each individual crystal. Here, we briefly summarize recent catalytic results from cracking and isomerization of alkalies......, alkylation of aromatics and present new results on isomerization of aromatics. Specifically, the shape-selective isomerization of meta-xylenc into para-xylene and ortho-xylene is studied. In all these reactions, rnesoporous zeolite single crystals prove to be unique catalysts since they provide easy...... transport to and from active sites and at the same time maintain the shape-selectivity required. Thus, all these results support the idea that the beneficial effect of the mesopores system in the mesoporous zeolite single crystals call be solely attributed to enhanced mass transport....

  13. Catalytic conversion of carbon dioxide to valuable chemicals

    Energy Technology Data Exchange (ETDEWEB)

    Baiker, A. [Swiss Federal Institute of Technology, Zuerich (Switzerland). Lab. of Technical Chemistry

    1999-08-01

    Fixation of carbon dioxide by using it as a C{sub 1}-building block in chemical synthesis has gained considerable interest, mainly stimulated by environmental considerations and by its abundant availability. Catalysis provides several opportunities to convert CO{sub 2} to valuable chemicals. The present state of these efforts is briefly surveyed giving special emphasis to most recent developments in heterogeneous catalysis, including the synthesis of methylmaines and formic acid derivatives. Chemicals synthesized by homogeneous catalysis mentioned are carbonates, carbamates, urethanes, lactones, pyrones, and formic acid and derivatives. Those made by heterogenous catalytic routes are: methanol, carbon monoxide and hydrogen (synthesis gas), methane, methylamine and formic acid derivatives. 70 refs., 1 fig.

  14. The use of non-fossil derived hydrogen in coal conversion processes

    Science.gov (United States)

    Harrison, J. S.; Merrick, D.; Smith, M.; Rasmussen, G.

    The National Coal Board, UK, carried out a technical and economic study of the use of non-fossil derived (NFD) hydrogen on three coal conversion processes: methanol synthesis, solid phase hydrogenation (hydrogasification) for substitute natural gas production, and liquid phase hydrogenation (liquifaction) for the manufacture of liquid fuels. Use of NFD hydrogen generally resulted in an increase in the conversion efficiency and carbon utilization, and a reduction in the number of component stages of the process. It was also shown that market conditions could exist in which the use of NFD hydrogen in coal conversion would be preferable to both conventional coal conversion and the direct use of hydrogen, irrespective of the coal price. Substitute natural gas production from synthesis gas (methanation) and the production of liquid fuels from synthesis gas by a Fischer-Tropsch synthesis route were also evaluated and showed similar technical and economic results. Preliminary results of the overall costs of using NFD hydrogen from a nuclear power/electrolysis plant showed that at present fuel prices, coal conversion processes using NFD hydrogen are not competitive with conventional processes, but would be if the price of coal were to double.

  15. Catalytic Conversion of Glucose into 5-Hydroxymethylfurfural by Hf(OTf4 Lewis Acid in Water

    Directory of Open Access Journals (Sweden)

    Junjie Li

    2015-12-01

    Full Text Available A series of Lewis acidic metal salts were used for glucose dehydration to 5-hydroymethylfurfural (HMF in water. Effect of valence state, ionic radii of Lewis acidic cation, and the type of anions on the catalytic performance have been studied systematically. The experimental results showed that the valence state played an important role in determining catalytic activity and selectivity. It was found that a higher glucose conversion rate and HMF selectivity could be obtained over high valent Lewis acid salts, where the ionic radii of these Lewis acidic metal salts are usually relatively small. Analysis on the effect of the anions of Lewis acid salts on the catalytic activity and the selectivity suggested that a higher glucose conversion and HMF selectivity could be readily obtained with Cl−. Furthermore, the recyclability of high valence state Lewis acid salt was also studied, however, inferior catalytic performance was observed. The deactivation mechanism was speculated to be the fact that high valence state Lewis acid salt was comparatively easier to undergo hydrolysis to yield complicated metal aqua ions with less catalytic activity. The Lewis acidic activity could be recovered by introducing a stoichiometric amount of hydrochloric acid (HCl to the catalytic before the reaction.

  16. One-Pot Catalytic Conversion of Cellulose and of Woody Biomass Solids to Liquid Fuels

    NARCIS (Netherlands)

    Matson, Theodore D.; Barta, Katalin; Iretskii, Alexei V.; Ford, Peter C.

    2011-01-01

    Efficient methodologies for converting biomass solids to liquid fuels have the potential to reduce dependence on imported petroleum while easing the atmospheric carbon dioxide burden. Here, we report quantitative catalytic conversions of wood and cellulosic solids to liquid and gaseous products in a

  17. Preparation of nitric humic acid by catalytic oxidation from Guizhou coal with catalysts

    Institute of Scientific and Technical Information of China (English)

    Yang Zhiyuan; Gong Liang; Ran Pan

    2012-01-01

    Nitric humic acid was prepared by catalytic oxidation between nitric acid and Guizhou coal,with added catalysts.We investigated catalytic oxidation processes and the factors that affect the reactions.The effects of different catalysts,including NiSO4 support on active carbon (AC-NiSO4),NiSO4 support on silicon dioxide (SiO2-NiSO4),composites of SO42-/Fe2O3,Zr-iron and vanadium-iron composite were studied.As well.we investigated nitric humic acid yields and the chemical structure of products by element analysis,FT-IR and E4/E6 (an absorbance ratio at wavelengths of 465 and 665 nm of humic acid alkaline extraction solutions).The results show that the catalytic oxidation reaction with added catalysts can increase humic acid yields by 18.7%,16.36%,12.94%,5.61% and 8.59%,respectively.The highest yield of humic acid,i.e.,36.0%,was obtained with AC-NiSO4 as the catalyst.The amounts of C and H decreased with the amount of nitrogen.The increase in the E4/E6 ratio in catalytic oxidation of (Guizhou) coal shows that small molecular weights and high yields of nitric humic acid can be obtained by catalytic oxidation reactions.

  18. Challenges of coal conversion for decarbonized energy in Poland

    Energy Technology Data Exchange (ETDEWEB)

    Sciazko, Marek; Jalosinski, Krzysztof; Majchrzak, Henryk; Michalski, Mieczyslaw; Tymowski, Henryk; Witos, Tadeusz; Wroblewska, Elzbieta

    2010-09-15

    Carbon dioxide is considered to be the main challenge for the coal-based power generation as well as for any other industrial application of coal. Poland's energy sector is primarily based on coal combustion that covers almost 90% of demand. Future development of that sector depends on the restriction on value of carbon dioxide emission or trading allowances. There are two main technological approaches to development of new coal based generation capacity, namely: gasification and pre-combustion capture; supercritical combustion and post-combustion capture. The current situation in development of three this type projects in Poland is presented.

  19. A comparison of thermal conversion process for several coal tar pitches

    Energy Technology Data Exchange (ETDEWEB)

    Feng, Y.; Shui, H.; Yuan, X. [East China Metallurgical Institute, Ma`anshan (China)

    1995-03-01

    The property and constituents of coal tar pitch are of great importance to the production of raw material for needle coke. Structural constituents of five coal tar pitches were determined using {sup 1}H-NMR. Besides, thermal conversion process of these pitches in which primary quinoline in soluble fraction was removed by centrifugal separation method was also investigated. The experimental results show Baogang (I) and Meishan coal tar pitches meet the requirements of raw material for needle coke. The thermal conversion data was correlated with structural parameters. 6 refs.,1 fig., 1 tab.

  20. Advanced Coal Conversion Process Demonstration Project. Technical progress report, January 1, 1993--December 31, 1993

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1995-02-01

    This report describes the technical progress made on the Advanced Coal Conversion Process (ACCP) Demonstration Project from January 1, 1993, through December 31, 1993. This project demonstrates an advanced, thermal, coal drying process, coupled with physical cleaning techniques, that is designed to upgrade high-moisture, low- rank coals to a high-quality, low-sulfur fuel, registered as the SynCoal{reg_sign} process. The coal is processed through three stages (two heating stages followed by an inert cooling stage) of vibrating fluidized bed reactors that remove chemically bound water, carboxyl groups, and volatile sulfur compounds. After thermal processing, the coal is put through a deep-bed stratifier cleaning process to separate the pyrite-rich ash from the coal. Rosebud SynCoal Partnership`s ACCP Demonstration Facility entered Phase III, Demonstration Operation, in April 1992 and operated in an extended startup mode through August 10, 1993, when the facility became commercial. Rosebud SynCoal Partnership instituted an aggressive program to overcome startup obstacles and now focuses on supplying product coal to customers. Significant accomplishments in the history of the SynCoal{reg_sign} process development are shown in Appendix A.

  1. Chemical coal conversion yesterday, today, and tomorrow; Der Chemierohstoff Kohle: gestern, heute und morgen

    Energy Technology Data Exchange (ETDEWEB)

    Talbiersky, J. [UCP Chemicals AG, Wien (Austria)

    2007-01-15

    Shortage in mineral oil and gas as well as a high price level have caused a renaissance in coal conversion technologies, at the end of the 70's. Today we have a similar situation. Now coal coversion technologies will be in the focus again but hopefully as a longterm strategy. The most important coal conversion technologies as liquefaction, gasification, coking and calcium carbide synthesis are discussed regarding their use for the production of chemicals. The most important source for aromatic chemicals from coal is till now coal tar with an availability of 22 Mio. t/a. The manufacturing of coal tar is discussed as an example for making aromatic products from a complex feed stock that you get by the fixed bed gasification, coal liquefaction and coking. Also the special marketing strategy that is necessary to be competitive against products from the petroindustry. It can be expected, that coal gasification as a source for synthesis gas will become more and more important. Synthesis gas is the access to aliphatic hydrocarbons by Fischer Tropsch synthesis and to methanol, a chemical with a high synthetic potential. Also the new hydrothermal carbonization of biomass to synthetic coal is mentioned. (orig.)

  2. Catalytic Conversion of Syngas into Higher Alcohols over Carbide Catalysts

    DEFF Research Database (Denmark)

    Christensen, Jakob Munkholt; Duchstein, Linus Daniel Leonhard; Wagner, Jakob Birkedal

    2012-01-01

    of carbonaceous deposits on the catalyst. At the same general activity level Li, K, and Cs provide similar promotional effects for Mo2C, although K at a loading level of alkali metal/Mo = 0.164 mol/mol provides the better behavior at equal conditions. The effect of further additives on the K2CO3/Mo2C system......This work investigates the use of the bulk carbides Mo2C, WC, and NbC as catalysts for the conversion of syngas into higher alcohols. K2CO3/WC produces mainly CH3OH and CH4 with a low activity. NbC has a very low activity in CO hydrogenation. K2CO3/Mo2C produces mixed alcohols with a reasonable...... activity and selectivity. In a 94 h test the activity and the specific surface area of the K2CO3/Mo2C catalyst decreased significantly, but X-ray diffraction and transmission electron microscopy did not indicate a strong sintering of the carbide. A likely cause for the deactivation is the formation...

  3. New directions for the catalytic conversion of methane

    Science.gov (United States)

    Lunsford, J. H.

    1992-02-01

    The addition of chlorine via HCl to a Li(+)-MgO catalyst improves its activity for the oxidative dehydrogenation (OXD) of ethane. The latter effect is greater than ethylene-to-ethane ratio (greater than 5) observed during the oxidative coupling reaction. During the OXD reaction at 620 C, an 80 percent conversion of C2H6 was achieved with 77 percent selectivity to C2H4 after 40 h on stream. To attain these favorable results, the Cl/Li ratio must be greater than or = 0.9. The absolute amounts of Li and Cl are of secondary importance, although an excess amount of promoters may serve to replace that which is slowly lost during the reaction. In the presence of chlorine, LiCl is formed rather than Li2CO3. The carbonate phase spreads over the surface and presumably blocks active sites. The chlorine in the catalyst also modifies the gross basicity of the catalyst, thus, making it less effective for the future oxidation of ethylene, which is the desired product.

  4. Catalytic activity of pyrite for coal liquefaction reaction; Tennen pyrite no shokubai seino ni kansuru kento

    Energy Technology Data Exchange (ETDEWEB)

    Hirano, K.; Kozu, M.; Okada, T.; Kobayashi, M. [Nippon Coal Oil Co. Ltd., Tokyo (Japan)

    1996-10-28

    Since natural pyrite is easy to obtain and cheap as coal liquefaction catalyst, it is to be used for the 150 t/d scale NEDOL process bituminous coal liquefaction pilot plant. NEDO and NCOL have investigated the improvement of catalytic activity of pulverized natural pyrite for enhancing performance and economy of the NEDOL process. In this study, coal liquefaction tests were conducted using natural pyrite catalyst pulverized by dry-type bowl mill under nitrogen atmosphere. Mechanism of catalytic reaction of the natural pyrite was discussed from relations between properties of the catalyst and liquefaction product. The natural pyrite provided an activity to transfer gaseous hydrogen into the liquefaction product. It was considered that pulverized pyrite promotes the hydrogenation reaction of asphaltene because pulverization increases its contact rate with reactant and the amount of active points on its surface. It was inferred that catalytic activity of pyrite is affected greatly by the chemical state of Fe and S on its surface. 3 refs., 4 figs., 1 tab.

  5. Measurement and modeling of advanced coal conversion processes, Volume II

    Energy Technology Data Exchange (ETDEWEB)

    Solomon, P.R.; Serio, M.A.; Hamblen, D.G. [and others

    1993-06-01

    A two dimensional, steady-state model for describing a variety of reactive and nonreactive flows, including pulverized coal combustion and gasification, is presented. The model, referred to as 93-PCGC-2 is applicable to cylindrical, axi-symmetric systems. Turbulence is accounted for in both the fluid mechanics equations and the combustion scheme. Radiation from gases, walls, and particles is taken into account using a discrete ordinates method. The particle phase is modeled in a lagrangian framework, such that mean paths of particle groups are followed. A new coal-general devolatilization submodel (FG-DVC) with coal swelling and char reactivity submodels has been added.

  6. The Investigation of Reducing PAHs Emission from Coal Pyrolysis by Gaseous Catalytic Cracking

    Directory of Open Access Journals (Sweden)

    Yulong Wang

    2014-01-01

    Full Text Available The catalytic cracking method of PAHs for the pyrolysis gaseous products is proposed to control their pollution to the environment. In this study, the Py-GC-MS is used to investigate in situ the catalytic effect of CaO and Fe2O3 on the 16 PAHs from Pingshuo coal pyrolysis under different catalytic temperatures and catalyst particle sizes. The results demonstrate that Fe2O3 is effective than that of CaO for catalytic cracking of 16 PAHs and that their catalytic temperature corresponding to the maximum PAHs cracking rates is different. The PAHs cracking rate is up to 60.59% for Fe2O3 at 600°C and is 52.88% at 700°C for CaO. The catalytic temperature and particle size of the catalysts have a significant effect on PAHs cracking rate and CaO will lose the capability of decreasing 16 PAHs when the temperature is higher than 900°C. The possible cracking process of 16 PAHs is deduced by elaborately analyzing the cracking effect of the two catalysts on 16 different species of PAHs.

  7. Catalytic conversion reactions in nanoporous systems with concentration-dependent selectivity: Statistical mechanical modeling

    Science.gov (United States)

    García, Andrés; Wang, Jing; Windus, Theresa L.; Sadow, Aaron D.; Evans, James W.

    2016-05-01

    Statistical mechanical modeling is developed to describe a catalytic conversion reaction A →Bc or Bt with concentration-dependent selectivity of the products, Bc or Bt, where reaction occurs inside catalytic particles traversed by narrow linear nanopores. The associated restricted diffusive transport, which in the extreme case is described by single-file diffusion, naturally induces strong concentration gradients. Furthermore, by comparing kinetic Monte Carlo simulation results with analytic treatments, selectivity is shown to be impacted by strong spatial correlations induced by restricted diffusivity in the presence of reaction and also by a subtle clustering of reactants, A .

  8. Coal liquefaction and gas conversion: Proceedings. Volume 1

    Energy Technology Data Exchange (ETDEWEB)

    1993-12-31

    Volume I contains papers presented at the following sessions: AR-Coal Liquefaction; Gas to Liquids; and Direct Liquefaction. Selected papers have been processed separately for inclusion in the Energy Science and Technology Database.

  9. Brown coal conversion by microwave plasma reactions under successive supply of methane

    Energy Technology Data Exchange (ETDEWEB)

    Kamei, O.; Onoe, K.; Marushima, W.; Yamaguchi, T. [Chiba institute of Technology, Chiba (Japan). Dept. of Industrial Chemistry

    1998-10-01

    To develop an innovative method for directly converting brown coal to relatively important fuels and synthesis gases in a single step, while simultaneously upgrading the carbon content of the residue, microwave plasma technology was applied to the direct conversion of brown coal (Yallourn). Methane under reduced pressure was supplied through a quartz reactor into the irradiation zone and reacted with the coal bed placed downstream. Both the coal conversion and the carbon content of the residue were increased with an increase of irradiation time. The yield of oily products showed a maximum value (18 wt.%) at 2 min irradiation, and the fuels were composed mainly of aliphatic hydrocarbons in the range from C{sub 13} to C{sub 34}. Furthermore, carbon monoxide and hydrogen accompanied by a molar fraction of {lt} 16% of acetylene were mainly produced when the irradiation time was varied from 1 to 10 min. 4 refs., 5 figs., 1 tab.

  10. Volatilisation and catalytic effects of alkali and alkaline earth metallic species during the pyrolysis and gasification of Victorian brown coal. Part IV. Catalytic effects of NaCl and ion-exchangeable Na in coal on char reactivity

    Energy Technology Data Exchange (ETDEWEB)

    Dimple Mody Quyn; Hongwei Wu; Jun-ichiro Hayashi; Chun-Zhu Li, [Monash University, Monash, Vic. (Australia). CRC for Clean Power from Lignite, Department of Chemical Engineering

    2003-03-01

    The purpose of this study is to investigate the catalytic effects of Na as NaCl or as sodium carboxylates ( COONa) in Victorian brown coal on the char reactivity. A Na-exchanged coal and a set of NaCl-loaded coal samples prepared from a Loy Yang brown coal were pyrolysed in a fluidised-bed/fixed-bed reactor and in a thermogravimetric analyser (TGA). The reactivities of the chars were measured in air at 400{sup o}C using the TGA. The experimental data indicate that the Na in coal as NaCl and as sodium carboxylates ( COONa) had very different catalytic effects on the char reactivity. It is the chemical form and dispersion of Na in char, not in coal, that govern the catalytic effects of Na. For the Na-form (Na-exchanged) coal, the char reactivity increased with increasing pyrolysis temperature from 500 to 700{sup o}C and then decreased with pyrolysis temperature from 700 to 900{sup o}C. The increase in reactivity with pyrolysis temperature (500 700{sup o}C) is mainly due to the changes in the relative distribution of Na in the char matrix and on the pore surface. For the NaCl-loaded coals, when Cl was released during pyrolysis or gasification, the Na originally present in coal as NaCl showed good catalytic effects for the char gasification. Otherwise, Cl would combine with Na in the char to form NaCl during gasification, preventing Na from becoming an active catalyst. Controlling the pyrolysis conditions to favour the release of Cl can be a promising way to transform NaCl in coal into an active catalyst for char gasification. 38 refs., 5 figs.

  11. Catalytic conversion of lignin pyrolysis model compound- guaiacol and its kinetic model including coke formation

    Science.gov (United States)

    Zhang, Huiyan; Wang, Yun; Shao, Shanshan; Xiao, Rui

    2016-11-01

    Lignin is the most difficult to be converted and most easy coking component in biomass catalytic pyrolysis to high-value liquid fuels and chemicals. Catalytic conversion of guaiacol as a lignin model compound was conducted in a fixed-bed reactor over ZSM-5 to investigate its conversion and coking behaviors. The effects of temperature, weight hourly space velocity (WHSV) and partial pressure on product distribution were studied. The results show the maximum aromatic carbon yield of 28.55% was obtained at temperature of 650 °C, WHSV of 8 h‑1 and partial pressure of 2.38 kPa, while the coke carbon yield was 19.55%. The reaction pathway was speculated to be removing methoxy group to form phenols with further aromatization to form aromatics. The amount of coke increased with increasing reaction time. The surface area and acidity of catalysts declined as coke formed on the acid sites and blocked the pore channels, which led to the decrease of aromatic yields. Finally, a kinetic model of guaiacol catalytic conversion considering coke deposition was built based on the above reaction pathway to properly predict product distribution. The experimental and model predicting data agreed well. The correlation coefficient of all equations were all higher than 0.90.

  12. Task 3.3: Warm Syngas Cleanup and Catalytic Processes for Syngas Conversion to Fuels Subtask 3: Advanced Syngas Conversion to Fuels

    Energy Technology Data Exchange (ETDEWEB)

    Lebarbier Dagel, Vanessa M.; Li, J.; Taylor, Charles E.; Wang, Yong; Dagle, Robert A.; Deshmane, Chinmay A.; Bao, Xinhe

    2014-03-31

    activity was to develop methods and enabling materials for syngas conversion to SNG with readily CO2 separation. Suitable methanation catalyst and CO2 sorbent materials were developed. Successful proof-of-concept for the combined reaction-sorption process was demonstrated, which culminated in a research publication. With successful demonstration, a decision was made to switch focus to an area of fuels research of more interest to all three research institutions (CAS-NETL-PNNL). Syngas-to-Hydrocarbon Fuels through Higher Alcohol Intermediates There are two types of processes in syngas conversion to fuels that are attracting R&D interest: 1) syngas conversion to mixed alcohols; and 2) syngas conversion to gasoline via the methanol-to-gasoline process developed by Exxon-Mobil in the 1970s. The focus of this task was to develop a one-step conversion technology by effectively incorporating both processes, which is expected to reduce the capital and operational cost associated with the conversion of coal-derived syngas to liquid fuels. It should be noted that this work did not further study the classic Fischer-Tropsch reaction pathway. Rather, we focused on the studies for unique catalyst pathways that involve the direct liquid fuel synthesis enabled by oxygenated intermediates. Recent advances made in the area of higher alcohol synthesis including the novel catalytic composite materials recently developed by CAS using base metal catalysts were used.

  13. Measurement and modeling of advanced coal conversion processes, Volume III

    Energy Technology Data Exchange (ETDEWEB)

    Ghani, M.U.; Hobbs, M.L.; Hamblen, D.G. [and others

    1993-08-01

    A generalized one-dimensional, heterogeneous, steady-state, fixed-bed model for coal gasification and combustion is presented. The model, FBED-1, is a design and analysis tool that can be used to simulate a variety of gasification, devolatilization, and combustion processes. The model considers separate gas and solid temperatures, axially variable solid and gas flow rates, variable bed void fraction, coal drying, devolatilization based on chemical functional group composition, depolymerization, vaporization and crosslinking, oxidation, and gasification of char, and partial equilibrium in the gas phase.

  14. Advanced Coal Conversion Process Demonstration Project. Final technical progress report, January 1, 1995--December 31, 1995

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-05-01

    This report describes the technical progress made on the Advanced Coal Conversion Process (ACCP) Demonstration Project from January 1, 1995 through December 31, 1995. This project demonstrates an advanced, thermal, coal upgrading process, coupled with physical cleaning techniques, that is designed to upgrade high-moisture, low-rank coals to a high-quality, low-sulfur fuel, registered as the SynCoal Process. The coal is processed through three stages (two heating stages followed by an inert cooling stage) of vibrating fluidized bed reactors that remove chemically bound water, carboxyl groups, and volatile sulfur compounds. After thermal upgrading, the coal is put through a deep-bed stratifier cleaning process to separate the pyrite-rich ash from the coal. The SynCoal Process enhances low-rank, western coals, usually with a moisture content of 25 to 55 percent, sulfur content of 0.5 to 1.5 percent, and heating value of 5,5000 to 9,000 British thermal units per pound (Btu/lb), by producing a stable, upgraded, coal product with a moisture content as low as 1 percent, sulfur content as low as 0.3 percent, and heating value up to 12,000 Btu/lb. During this reporting period, the primary focus for the ACCP Demonstration Project team was to expand SynCoal market awareness and acceptability for both the products and the technology. The ACCP Project team continued to focus on improving the operation, developing commercial markets, and improving the SynCoal products as well as the product`s acceptance.

  15. Catalytic oxidation of gaseous reduced sulfur compounds using coal fly ash.

    Science.gov (United States)

    Kastner, James R; Das, K C; Melear, Nathan D

    2002-11-11

    Activated carbon has been shown to oxidize reduced sulfur compounds, but in many cases it is too costly for large-scale environmental remediation applications. Alternatively, we theorized that coal fly ash, given its high metal content and the presence of carbon could act as an inexpensive catalytic oxidizer of reduced sulfur compounds for "odor" removal. Initial results indicate that coal fly ash can catalyze the oxidization of H(2)S and ethanethiol, but not dimethyl sulfide (DMS) and dimethyl disulfide (DMDS) at room temperature. In batch reactor systems, initial concentrations of 100-500 ppmv H(2)S or ethanethiol were reduced to 0-2 ppmv within 1-2 and 6-8 min, respectively. This was contrary to control systems without ash in which concentrations remained constant. Diethyl disulfide was formed from ethanethiol substantiating the claim that catalytic oxidation occurred. The presence of water increased the rate of adsorption/reaction of both H(2)S and ethanethiol for the room temperature reactions (23-25 degrees C). Additionally, in a continuous flow packed bed reactor, a gaseous stream containing an inlet H(2)S concentration of 400-500 ppmv was reduced to 200 ppmv at a 4.6s residence time. The removal efficiency remained at 50% for approximately 4.6h or 3500 reactor volumes. These results demonstrate the potential of using coal fly ash in reactors for removal of H(2)S and other reduced sulfur compounds.

  16. Conversion Excess Coal Gas to Dimethyl Ether in Steel Works

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    With the technical progress of metallurgical industry, more excess gas will be produced in steel works. The feasibility of producing dimethyl ether by gas synthesis was discussed, which focused on marketing, energy balance, process design, economic evaluation, and environmental protection etc. DME was considered to be a new way to utilize excess coal gas in steel works.

  17. Catalytic activity of carbon nanotubes in the conversion of aliphatic alcohols

    Science.gov (United States)

    Zhitnev, Yu. N.; Tveritinova, E. A.; Chernyak, S. A.; Savilov, S. V.; Lunin, V. V.

    2016-06-01

    Carbon nanotubes (CNTs) obtained via the catalytic pyrolysis of hexane at 750°C were studied as the catalysts in conversion of C2-C4 alcohols. The efficiency of CNTs as catalysts in dehydration and dehydrogenation of ethanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol, and tert-butanol was studied by means of pulse microcatalysis. The surface and structural characteristics of CNTs are investigated via SEM, TEM, DTA, BET, and XPS. CNTs are shown to be effective catalysts in the conversion of alcohols and do not require additional oxidative treatment. The regularities of the conversion of aliphatic alcohols, related to the properties of the CNTs surface and the structure of the alcohols are identified.

  18. A thermogravimetric analysis (TGA) method to determine the catalytic conversion of cellulose from carbon-supported hydrogenolysis process

    Energy Technology Data Exchange (ETDEWEB)

    Leal, Glauco F. [Brazilian Synchrotron Light Laboratory (LNLS), Brazilian Center for Research in Energy and Materials (CNPEM), C.P. 6192, 13083-970 Campinas, SP (Brazil); Institute of Chemistry of São Carlos (IQSC), University of São Paulo (USP), C.P. 780, CEP 13560-970 São Carlos, SP (Brazil); Ramos, Luiz A. [Institute of Chemistry of São Carlos (IQSC), University of São Paulo (USP), C.P. 780, CEP 13560-970 São Carlos, SP (Brazil); Barrett, Dean H. [Brazilian Synchrotron Light Laboratory (LNLS), Brazilian Center for Research in Energy and Materials (CNPEM), C.P. 6192, 13083-970 Campinas, SP (Brazil); Curvelo, Antonio Aprígio S. [Institute of Chemistry of São Carlos (IQSC), University of São Paulo (USP), C.P. 780, CEP 13560-970 São Carlos, SP (Brazil); Brazilian Bioethanol Science and Technology Laboratory (CTBE), Brazilian Center for Research in Energy and Materials (CNPEM), C.P. 6179, 13083-970 Campinas, SP (Brazil); Rodella, Cristiane B., E-mail: cristiane.rodella@lnls.br [Brazilian Synchrotron Light Laboratory (LNLS), Brazilian Center for Research in Energy and Materials (CNPEM), C.P. 6192, 13083-970 Campinas, SP (Brazil)

    2015-09-20

    Graphical abstract: - Highlights: • A new method to determine the catalytic conversion of cellulose using TGA has been developed. • TGA is able to differentiate between carbon from cellulose and carbon from the catalyst. • Building an analytical curve from TGA results enables the accurate determination of cellulose conversion. - Abstract: The ability to determine the quantity of solid reactant that has been transformed after a catalytic reaction is fundamental in accurately defining the conversion of the catalyst. This quantity is also central when investigating the recyclability of a solid catalyst as well as process control in an industrial catalytic application. However, when using carbon-supported catalysts for the conversion of cellulose this value is difficult to obtain using only a gravimetric method. The difficulty lies in weighing errors caused by loss of the solid mixture (catalyst and non-converted cellulose) after the reaction and/or moisture adsorption by the substrate. These errors are then propagated into the conversion calculation giving erroneous results. Thus, a quantitative method using thermogravimetric analysis (TGA) has been developed to determine the quantity of cellulose after a catalytic reaction by using a tungsten carbide catalyst supported on activated carbon. Stepped separation of TGA curves was used for quantitative analysis where three thermal events were identified: moisture loss, cellulose decomposition and CO/CO{sub 2} formation. An analytical curve was derived and applied to quantify the residual cellulose after catalytic reactions which were performed at various temperatures and reaction times. The catalytic conversion was calculated and compared to the standard gravimetric method. Results showed that catalytic cellulose conversion can be determined using TGA and exhibits lower uncertainty (±2%) when compared to gravimetric determination (±5%). Therefore, it is a simple and relatively inexpensive method to determine

  19. Conversion of an Existing Gas Turbine to an Intercooled Exhaust-Heated Coal-Burning Engine

    Science.gov (United States)

    1990-12-01

    possibilities of using biomass is also included. The engine chosen for conversion is the 2.8 MW F olar 5650 industrial gas turbine. The conversion... alkali -laden gas which can result in particulate and chemical action on the turbine as well as pollution. Particulate matter has a powerful erosive effect...rate is then adjusted by altering the pressure difference between the tank and the carrier line at the orifice [45]. Pretreatment of the coal is

  20. Prominent roles of impurities in ionic liquid for catalytic conversion of carbohydrates

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Haibo; Brown, Heather M.; Holladay, Johnathan E.; Zhang, Z. Conrad

    2012-02-07

    In the last two decades, ionic liquids have emerged as new and versatile solvents, and many of them are also catalysts for a broad range of catalytic reactions. Certain ionic liquids have been found to possess the unique capability of dissolving cellulosic biomass. The potential of such ionic liquids as solvent to enable catalytic conversion of cellulosic polymers was first explored and demonstrated by Zhao et al. This field of research has since experienced a rapid growth. Most ionic liquids have negligible vapor pressure and excellent thermal stability over a wide temperature range. For example, ionic liquids composed of 1-ethyl-3-methylimidazolium (EMIM+) cation and Cl- anion was reported to be stable up to 285 C, while salts of the same cation with other anions such as BF4- and PF6- are thermally stable above 380 C under inert atmosphere. It is well known that presence of impurities in ionic liquids typically causes changes in physical properties, e.g. decreasing in melting point and viscosity. Addition of Lewis acidic metal chlorides, e.g. AlCl3 to 1-alkyl-3-methylimidazolium chloride, [AMIM]Cl, is an exothermic reaction and considerably reduces the melting point by forming [AMIM]AlCl4 or [AMIM]Al2Cl7 that are also ionic liquids but have much lower melting point than the parent [AMIM]Cl. While most early research on catalysis of ionic liquids involving metallohalide anions were typically conducted from stoichiometric ratio of such anions to organic cations, e.g. [AMIM]+, the use of pure ionic liquids only as a solvent to carry out catalysis by a catalytic amount of a metal halide as catalyst truly displayed the solvent property of such ionic liquids.4 In such reaction systems, catalytic amounts of metal halides were used to catalyze the conversion of glucose and cellulose.4,11,12 The metal chloride catalyst concentration was in the order of 10-3 M. The presence of another metal chloride in the ionic liquids, even in the order of 10-5 M concentration was found

  1. DEVELOPMENT OF ATOM-ECONOMICAL CATALYTIC PATHWAYS FOR CONVERSIONS OF SYNGAS TO ENERGY LIQUIDS

    Energy Technology Data Exchange (ETDEWEB)

    MAHAJAN,D.; WEGRZYN,J.E.; LEE,T.; GUREVICH,M.

    1999-03-01

    The subject of catalytic syngas conversions to fuels and chemicals is well studied (1--3). But globally, the recent focus is on development of technologies that offer an economical route to desired products (4). Economical transport of natural gas from remote locations and within clathrate hydrates is of continuing interest at Brookhaven National Laboratory (BNL). Under this project, a Liquid Phase Low Temperature (LPLT) concept is being applied to attain highly efficient transformations of natural-gas derived syngas to specific products. Furthermore, a more precise term ``Atom Economy'' has been recently introduced by Trost to describe development of highly efficient homogeneously catalyzed synthesis of organic molecules (5). Taken from reference 5, the term ``Atom Economy'' is defined as maximizing the number of atoms of all raw materials that end up in the product with any other reactant required on in catalytic amount. For application to methane transformations that may involve one or more steps, atom economy of each of these steps is critical. The authors, therefore, consider atom-economy synonymous with overall energy efficiency of a process. This paper describes potential liquid products from catalytic syngas conversions, i.e. gas to liquids (GTL) technologies and process considerations that are necessary for economical transport of natural gas. As such, the present study defines an atom-economical standard to directly compare competing GTL technologies.

  2. Carbon Dioxide Conversion to Valuable Chemical Products over Composite Catalytic Systems

    Energy Technology Data Exchange (ETDEWEB)

    Dagle, Robert A.; Hu, Jianli; Jones, Susanne B.; Wilcox, Wayne A.; Frye, John G.; White, J. F.; Jiang, Juyuan; Wang, Yong

    2013-05-01

    Presented is an experimental study on catalytic conversion of carbon dioxide into methanol, ethanol and acetic acid. Catalysts having different catalytic functions were synthesized and combined in different ways to enhance selectivity to desired products. The combined catalyst system possessed the following functions: methanol synthesis, Fischer-Tropsch synthesis, water-gas-shift and hydrogenation. Results showed that the methods of integrating these catalytic functions played important role in achieving desired product selectivity. It was speculated that if methanol synthesis sites were located adjacent to the C-C chain growth sites, the formation rate of C2 oxygenates would be enhanced. The advantage of using high temperature methanol catalyst PdZnAl in the combined catalyst system was demonstrated. In the presence of PdZnAl catalyst, the combined catalyst system was stable at temperature of 380oC. It was observed that, at high temperature, kinetics favored oxygenate formation. Results implied that the process can be intensified by operating at high temperature using Pd-based methanol synthesis catalyst. Steam reforming of the byproduct organics was demonstrated as a means to provide supplemental hydrogen. Preliminary process design, simulation, and economic analysis of the proposed CO2 conversion process were carried out. Economic analysis indicates how ethanol production cost was affected by the price of CO2 and hydrogen.

  3. Dual-Bed Catalytic System for Direct Conversion of Methane to Liquid Hydrocarbons

    Institute of Scientific and Technical Information of China (English)

    N.A.S.Amin; Sriraj Ammasi

    2006-01-01

    A dual-bed catalytic system is proposed for the direct conversion of methane to liquid hydrocarbons. In this system, methane is converted in the first stage to oxidative coupling of methane (OCM) products by selective catalytic oxidation with oxygen over La-supported MgO catalyst. The second bed, comprising of the HZSM-5 zeolite catalyst, is used for the oligomerization of OCM light hydrocarbon products to liquid hydrocarbons. The effects of temperature (650-800 ℃), methane to oxygen ratio (4-10), and SiO2/Al2O3 ratio of the HZSM-5 zeolite catalyst on the process are studied. At higher reaction temperatures, there is considerable dealumination of HZSM-5, and thus its catalytic performance is reduced. The acidity of HZSM-5 in the second bed is responsible for the oligomerization reaction that leads to the formation of liquid hydrocarbons. The activities of the oligomerization sites were unequivocally affected by the SiO2/Al2O3 ratio. The relation between the acidity and the activity of HZSM-5 is studied by means of TPD-NH3 techniques. The rise in oxygen concentration is not beneficial for the C5+ selectivity, where the combustion reaction of intermediate hydrocarbon products that leads to the formation of carbon oxide (CO+CO2) products is more dominant than the oligomerization reaction. The dual-bed catalytic system is highly potential for directly converting methane to liquid fuels.

  4. Rationale for continuing R&D in direct coal conversion to produce high quality transportation fuels

    Energy Technology Data Exchange (ETDEWEB)

    Srivastava, R.D.; McIlvried, H.G. [Burns and Roe Services Corp., Pittsburgh, PA (United States); Gray, D. [Mitre Corp, McLean, VA (United States)] [and others

    1995-12-31

    For the foreseeable future, liquid hydrocarbon fuels will play a significant role in the transportation sector of both the United States and the world. Factors favoring these fuels include convenience, high energy density, and the vast existing infrastructure for their production and use. At present the U.S. consumes about 26% of the world supply of petroleum, but this situation is expected to change because of declining domestic production and increasing competition for imports from countries with developing economies. A scenario and time frame are developed in which declining world resources will generate a shortfall in petroleum supply that can be allieviated in part by utilizing the abundant domestic coal resource base. One option is direct coal conversion to liquid transportation fuels. Continued R&D in coal conversion technology will results in improved technical readiness that can significantly reduce costs so that synfuels can compete economically in a time frame to address the shortfall.

  5. Simulation of coal conversion in Ar/H{sub 2} plasma jet

    Energy Technology Data Exchange (ETDEWEB)

    Tian, Y.J.; Chen, H.G.; Bao, W.R.; Li, F.; Zhu, S.Y.; Xie, K.C. [Taiyuan University of Technology, Taiyuan (China). Shanxi Key Lab of Coal Science and Technology

    1999-07-01

    Coal conversion arc plasma was estimated by the combination of energy balance and chemical percolation devolatilization model. The velocity of particles was calculated by momentum equations and the temperature of particles and plasma jet was calculated by heat transfer equations. 11 refs., 2 figs., 4 tabs.

  6. Proceedings of the 2nd symposium on valves for coal conversion and utilization

    Energy Technology Data Exchange (ETDEWEB)

    Maxfield, D.A. (ed.)

    1981-01-01

    The 2nd symposium on valves for coal conversion and utilization was held October 15 to 17, 1980. It was sponsored by the US Department of Energy, Morgantown Energy Technology Center, in cooperation with the Valve Manufacturers Association. Seventeen papers have been entered individually into EDB and ERA. (LTN)

  7. Recent developments in the production of liquid fuels via catalytic conversion of microalgae: experiments and simulations

    Energy Technology Data Exchange (ETDEWEB)

    Shi, Fan; Wang, Pin; Duan, Yuhua; Link, Dirk; Morreale, Bryan

    2012-01-01

    Due to continuing high demand, depletion of non-renewable resources and increasing concerns about climate change, the use of fossil fuel-derived transportation fuels faces relentless challenges both from a world markets and an environmental perspective. The production of renewable transportation fuel from microalgae continues to attract much attention because of its potential for fast growth rates, high oil content, ability to grow in unconventional scenarios, and inherent carbon neutrality. Moreover, the use of microalgae would minimize ‘‘food versus fuel’’ concerns associated with several biomass strategies, as microalgae do not compete with food crops in the food chain. This paper reviews the progress of recent research on the production of transportation fuels via homogeneous and heterogeneous catalytic conversions of microalgae. This review also describes the development of tools that may allow for a more fundamental understanding of catalyst selection and conversion processes using computational modelling. The catalytic conversion reaction pathways that have been investigated are fully discussed based on both experimental and theoretical approaches. Finally, this work makes several projections for the potential of various thermocatalytic pathways to produce alternative transportation fuels from algae, and identifies key areas where the authors feel that computational modelling should be directed to elucidate key information to optimize the process.

  8. CATALYTIC CONVERSION OF FORMIC ACID TO METHANOL WITH Cu AND Al UNDER HYDROTHERMAL CONDITIONS

    Directory of Open Access Journals (Sweden)

    Hansong Yao,

    2012-01-01

    Full Text Available Catalytic conversion of formic acid into methanol was investigated with Cu as a catalyst and Al as a reductant under hydrothermal conditions. It was found that formic acid can be converted into methanol by such means. The highest yield of methanol (30.4% was attained with a temperature of 300 °C and a reaction time of 9 h. The AlO(OH formed from Al oxidation may also play a catalytic role in the formation of methanol. This process may provide a promising solution to producing methanol from carbohydrate biomass combined with the process of converting the carbohydrate into formic acid, which is expected to emit no CO2.

  9. Catalytic conversion of light alkanes, Phase 1. Topical report, January 1990--January 1993

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1993-12-31

    The authors have found a family of new catalytic materials which, if successfully developed, will be effective in the conversion of light alkanes to alcohols or other oxygenates. Catalysts of this type have the potential to convert natural gas to clean-burning high octane liquid fuels directly without requiring the energy-intensive steam reforming step. In addition they also have the potential to upgrade light hydrocarbons found in natural gas to a variety of high value fuel and chemical products. In order for commercially useful processes to be developed, increases in catalytic life, reaction rate and selectivity are required. Recent progress in the experimental program geared to the further improvement of these catalysts is outlined.

  10. Catalytic Conversion of Biomass to Fuels and Chemicals Using Ionic Liquids

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Wei; Zheng, Richard; Brown, Heather; Li, Joanne; Holladay, John; Cooper, Alan; Rao, Tony

    2012-04-13

    This project provides critical innovations and fundamental understandings that enable development of an economically-viable process for catalytic conversion of biomass (sugar) to 5-hydroxymethylfurfural (HMF). A low-cost ionic liquid (Cyphos 106) is discovered for fast conversion of fructose into HMF under moderate reaction conditions without any catalyst. HMF yield from fructose is almost 100% on the carbon molar basis. Adsorbent materials and adsorption process are invented and demonstrated for separation of 99% pure HMF product and recovery of the ionic liquid from the reaction mixtures. The adsorbent material appears very stable in repeated adsorption/regeneration cycles. Novel membrane-coated adsorbent particles are made and demonstrated to achieve excellent adsorption separation performances at low pressure drops. This is very important for a practical adsorption process because ionic liquids are known of high viscosity. Nearly 100% conversion (or dissolution) of cellulose in the catalytic ionic liquid into small molecules was observed. It is promising to produce HMF, sugars and other fermentable species directly from cellulose feedstock. However, several gaps were identified and could not be resolved in this project. Reaction and separation tests at larger scales are needed to minimize impacts of incidental errors on the mass balance and to show 99.9% ionic liquid recovery. The cellulose reaction tests were troubled with poor reproducibility. Further studies on cellulose conversion in ionic liquids under better controlled conditions are necessary to delineate reaction products, dissolution kinetics, effects of mass and heat transfer in the reactor on conversion, and separation of final reaction mixtures.

  11. Research on coal staged conversion poly-generation system based on fluidized bed

    Institute of Scientific and Technical Information of China (English)

    Mingjiang Ni; Chao Li; Mengxiang Fang; Qinhui Wang; Zhongyang Luo; Kefa Cen

    2014-01-01

    A new coal staged conversion poly-generation system combined coal combustion and pyrolysis has been developed for clean and high efficient utilization of coal. Coal is the first pyrolysed in a fluidized pyrolyzer. The pyrolysis gas is then purified and used for chemical product or liquid fuel production. Tar is collected during purification and can be processed to extract high value product and to make liquid fuels by hydro-refining. Semi-coke from the pyrolysis reactor is burned in a circulating fluidized bed (CFB) combustor for heat or power generation. The system can realize coal multi-product generation and has a great potential to increase coal utilization value. A 1 MW poly-generation system pilot plant and a 12 MW CFB gas, tar, heat and power poly-generation system was erected. The experimental study focused on the two fluidized bed operation and characterization of gas, tar and char yields and compositions. The results showed that the system could operate stable, and produce about 0.12 m3/kg gas with 22 MJ/m3 heating value and about 10 wt%tar when using Huainan bituminous coal under pyrolysis temperature between 500 and 600 ?C. The produced gases were mainly H2, CH4, CO, CO2, C2H4, C2H6, C3H6 and C3H8. The CFB combustor can burn semi-coke steadily. The application prospect of the new system was discussed.

  12. Catalytic conversion of aliphatic alcohols on carbon nanomaterials: The roles of structure and surface functional groups

    Science.gov (United States)

    Tveritinova, E. A.; Zhitnev, Yu. N.; Chernyak, S. A.; Arkhipova, E. A.; Savilov, S. V.; Lunin, V. V.

    2017-03-01

    Carbon nanomaterials with the structure of graphene and different compositions of the surface groups are used as catalysts for the conversion of C2-C4 aliphatic alcohols. The conversions of ethanol, propanol- 1, propanol-2, butanol-1, butanol-2, and tert-butanol on carbon nanotubes, nanoflakes, and nanoflakes doped with nitrogen are investigated. Oxidized and nonoxidized multiwalled carbon nanotubes, nanoflakes, and nanoflakes doped with nitrogen are synthesized. X-ray diffraction analysis, X-ray photoelectron spectroscopy, scanning and transmission electronic microscopies, Brunauer-Emmett-Teller method, derivatographic analyses, and the pulsed microcatalytic method are used to characterize comprehensively the prepared catalysts. It was established that all of the investigated carbon nanomaterials (with the exception of nondoped carbon nanoflakes) are bifunctional catalysts for the conversion of aliphatic alcohols, and promote dehydration reactions with the formation of olefins and dehydrogenation reactions with the formation of aldehydes or ketones. Nanoflakes doped with nitrogen are inert with respect to secondary alcohols and tert-butanol. The role of oxygen-containing and nitrogen-containing surface groups, and of the geometrical structure of the carbon matrix of graphene nanocarbon materials in the catalytic conversion of aliphatic alcohols, is revealed. Characteristics of the conversion of aliphatic alcohols that are associated with their structure are identified.

  13. Tunable catalytic properties of bi-functional mixed oxides in ethanol conversion to high value compounds

    Energy Technology Data Exchange (ETDEWEB)

    Ramasamy, Karthikeyan K.; Gray, Michel J.; Job, Heather M.; Smith, Colin D.; Wang, Yong

    2016-04-10

    tA highly versatile ethanol conversion process to selectively generate high value compounds is pre-sented here. By changing the reaction temperature, ethanol can be selectively converted to >C2alcohols/oxygenates or phenolic compounds over hydrotalcite derived bi-functional MgO–Al2O3cata-lyst via complex cascade mechanism. Reaction temperature plays a role in whether aldol condensationor the acetone formation is the path taken in changing the product composition. This article containsthe catalytic activity comparison between the mono-functional and physical mixture counterpart to thehydrotalcite derived mixed oxides and the detailed discussion on the reaction mechanisms.

  14. Factors Influencing Conversion of Pyritic Sulfur in Coal by Microwave Irradiation

    Institute of Scientific and Technical Information of China (English)

    SUI Jian-cai; XU Ming-hou; QIU Ji-hua; CHENG Rong

    2005-01-01

    The high sulfur coal from southwest of China was used to examine the influence of different factors such as irradiation time, particle size of coal, and leachant (Na2CO3, NaOH and CuCl2.2H2O)on the conversion rate of pyrite to pyrrhotite by microwave irradiation. Single factor experiment was performed firstly, then orthogonal test method was used to explore these factors. The result shows that the optimal treating conditions for the conversion are a treatment time of 3 min, a particle size from 0.086 mm to 0.102 mm, and a favorable leachant of sodium hydroxide. Under these conditions the conversion rate of pyrite can reach 45.7 %.

  15. Catalytic oxidative conversion of cellulosic biomass to formic acid and acetic acid with exceptionally high yields

    KAUST Repository

    Zhang, Jizhe

    2014-09-01

    Direct conversion of raw biomass materials to fine chemicals is of great significance from both economic and ecological perspectives. In this paper, we report that a Keggin-type vanadium-substituted phosphomolybdic acid catalyst, namely H4PVMo11O40, is capable of converting various biomass-derived substrates to formic acid and acetic acid with high selectivity in a water medium and oxygen atmosphere. Under optimized reaction conditions, H4PVMo11O40 gave an exceptionally high yield of formic acid (67.8%) from cellulose, far exceeding the values achieved in previous catalytic systems. Our study demonstrates that heteropoly acids are generally effective catalysts for biomass conversion due to their strong acidities, whereas the composition of metal addenda atoms in the catalysts has crucial influence on the reaction pathway and the product selectivity. © 2013 Elsevier B.V.

  16. Catalytic conversion of carbohydrates into 5-hydroxymethylfurfural by germanium(IV) chloride in ionic liquids.

    Science.gov (United States)

    Zhang, Zehui; Wang, Qian; Xie, Haibo; Liu, Wujun; Zhao, Zongbao Kent

    2011-01-17

    Direct conversion of carbohydrates into 5-hydroxymethylfurfural (HMF) catalyzed by germanium(IV) chloride in ionic liquids has been investigated in search of an efficient and environmentally friendly process. Monosaccharides D-fructose and D-glucose, disaccharides sucrose and maltose, and even the polysaccharide cellulose were successfully converted into HMF with good yields under mild conditions (yield up to 92 % in 5 min in the case of fructose). The structure of ionic liquids, catalyst loading, reaction temperature and water content had noticeable effects on this catalytic system. Addition of 5 Å molecular sieves during the dehydration of glucose resulted in an increase in HMF yield from 38.4 % to 48.4 %. A mechanism for glucose conversion to HMF catalyzed by germanium(IV) chloride was proposed according to ¹³C NMR spectra obtained in situ under different conditions using D-glucose-2-¹³C as the substrate.

  17. Production of aromatics through current-enhanced catalytic conversion of bio-oil tar.

    Science.gov (United States)

    Bi, Peiyan; Yuan, Yanni; Fan, Minghui; Jiang, Peiwen; Zhai, Qi; Li, Quanxin

    2013-05-01

    Biomass conversion into benzene, toluene and xylenes (BTX) can provide basic feedstocks for the petrochemical industry, which also serve as the most important aromatic platform molecules for development of high-end chemicals. Present work explored a new route for transformation of bio-oil tar into BTX through current-enhanced catalytic conversion (CECC), involving the synergistic effect between the zeolite catalyst and current to promote the deoxygenation and cracking reactions. The proposed transformation shows an excellent BTX aromatics selectivity of 92.9 C-mol% with 25.1 wt.% yield at 400 °C over usual HZSM-5 catalyst. The study of the model compounds revealed that the groups such as methoxy, hydroxyl and methyl in aromatics can be effectively removed in the CECC process. Present transformation potentially provides an important approach for production of the key petrochemicals of BTX and the overall use of bio-oil tar derived from bio-oil or biomass.

  18. Biodiesel production from algae oil high in free fatty acids by two-step catalytic conversion.

    Science.gov (United States)

    Chen, Lin; Liu, Tianzhong; Zhang, Wei; Chen, Xiaolin; Wang, Junfeng

    2012-05-01

    The effect of storage temperature and time on lipid composition of Scenedesmus sp. was studied. When stored at 4°C or higher, the free fatty acid content in the wet biomass increased from a trace to 62.0% by day 4. Using two-step catalytic conversion, algae oil with a high free fatty acid content was converted to biodiesel by pre-esterification and transesterification. The conversion rate of triacylglycerols reached 100% under the methanol to oil molar ratio of 12:1 during catalysis with 2% potassium hydroxide at 65°C for 30 min. This process was scaled up to produce biodiesel from Scenedesmus sp. and Nannochloropsis sp. oil. The crude biodiesel was purified using bleaching earth. Except for moisture content, the biodiesel conformed to Chinese National Standards.

  19. Catalytic hydroprocessing of SRC-II heavy distillate fractions: Conversion of the acidic fractions characterized by gas chromatography/mass spectrometry

    Energy Technology Data Exchange (ETDEWEB)

    Grandy, D.W.; Petrakis, L.; Li, C.; Gates, B.C.

    1986-01-01

    Kinetics data have been determined for the catalytic hydroprocessing of the acidic fractions of a heavy distillate of a liquid derived from Powhatan No. 5 coal. A commercial, sulfided Ni-Mo/..gamma..-Al/sub 2/O/sub 3/ catalyst was used in the experiments, carried out at 350/sup 0/C and 120 atm with the coal liquid fractions dissolved in cyclohexane. The feed and hydrotreated products were analyzed by gas chromatography/mass spectrometry. The data were analyzed with group-type methods for compound classes, and results were also obtained for some individual organooxygen compounds. Catalytic hydroprocessing leads to a large increase in the number of compounds and a shift to lower boiling ranges. The data are broadly consistent with reaction networks determined with pure compounds; the most important reactions include aromatic ring hydrogenation, hydrodeoxygenation, and hydrodemethylation. Pseudo-first-order rate constants for conversion of the predominant organooxygen coupounds are on the order of 10/sup -4/ L/(g of catalysts); the reactivity decreases in the order cyclohexylphenol > dimethylhydroxyindan > tetrahydronaphthol > phenylphenol > 1-naphthol.

  20. Catalytic Two-Stage Liquefaction (CTSL) process bench studies with bituminous coal. Final report, [October 1, 1988--December 31, 1992

    Energy Technology Data Exchange (ETDEWEB)

    Comolli, A.G.; Johanson, E.S.; Karolkiewicz, W.F.; Lee, L.K.; Stalzer, R.H.; Smith, T.O.

    1993-03-01

    Reported herein are the details and results of Laboratory and Bench-Scale experiments using bituminous coal concluded at Hydrocarbon Research, Inc., under DOE contract during the period October 1, 1988 to December 31, 1992. The work described is primarily concerned with the application of coal cleaning methods and solids separation methods to the Catalytic Two-Stage Liquefaction (CTSL) Process. Additionally a predispersed catalyst was evaluated in a thermal/catalytic configuration, and an alternative nickel molybdenum catalyst was evaluated for the CTSL process. Three coals were evaluated in this program: Bituminous Illinois No. 6 Burning Star and Sub-bituminous Wyoming Black Thunder and New Mexico McKinley Mine seams. The results from a total of 16 bench-scale runs are reported and analyzed in detail. The tests involving the Illinois coal are reported herein, and the tests involving the Wyoming and New Mexico coals are described in Topical Report No. 1. On the laboratory scale, microautoclave tests evaluating coal, start-up oils, catalysts, thermal treatment, CO{sub 2} addition and sulfur compound effects are reported in Topical Report No. 3. Other microautoclave tests, such as tests on rejuvenated catalyst, coker liquids, and cleaned coals, are described in the Bench Run sections to which they refer. The microautoclave tests conducted for modelling the CTSL process are described in the CTSL Modelling section of Topical Report No. 3 under this contract.

  1. A characterization and evaluation of coal liquefaction process streams. The kinetics of coal liquefaction distillation resid conversion

    Energy Technology Data Exchange (ETDEWEB)

    Klein, M.T.; Calkins, W.H.; Huang, H.; Wang, S.; Campbell, D.

    1998-03-01

    Under subcontract from CONSOL Inc., the University of Delaware studied the mechanism and kinetics of coal liquefaction resid conversion. The program at Delaware was conducted between August 15, 1994, and April 30, 1997. It consisted of two primary tasks. The first task was to develop an empirical test to measure the reactivity toward hydrocracking of coal-derived distillation resids. The second task was to formulate a computer model to represent the structure of the resids and a kinetic and mechanistic model of resid reactivity based on the structural representations. An introduction and Summary of the project authored by CONSOL and a report of the program findings authored by the University of Delaware researchers are presented here.

  2. System Study of Rich Catalytic/Lean burn (RCL) Catalytic Combustion for Natural Gas and Coal-Derived Syngas Combustion Turbines

    Energy Technology Data Exchange (ETDEWEB)

    Shahrokh Etemad; Lance Smith; Kevin Burns

    2004-12-01

    Rich Catalytic/Lean burn (RCL{reg_sign}) technology has been successfully developed to provide improvement in Dry Low Emission gas turbine technology for coal derived syngas and natural gas delivering near zero NOx emissions, improved efficiency, extending component lifetime and the ability to have fuel flexibility. The present report shows substantial net cost saving using RCL{reg_sign} technology as compared to other technologies both for new and retrofit applications, thus eliminating the need for Selective Catalytic Reduction (SCR) in combined or simple cycle for Integrated Gasification Combined Cycle (IGCC) and natural gas fired combustion turbines.

  3. Conversion of the refractory ammonia and acetic acid in catalytic wet air oxidation of animal byproducts.

    Science.gov (United States)

    Fontanier, Virginie; Zalouk, Sofiane; Barbati, Stéphane

    2011-01-01

    Wet air oxidation (WAO) and catalytic wet air oxidation (CWAO) of slaughtered animal byproducts (ABPs) were investigated. Two step experiment was carried out consisting of a non-catalysed WAO run followed by a CWAO run at 170-275 degrees C, 20 MPa, and reaction time 180 min. The WAO (1st step) of sample (5 g/L total organic carbon (TOC)) yielded (82.0 +/- 4)% TOC removal and (78.4 +/- 13.2)% conversion of the initial organic-N into NH4(+)-N. Four metal catalysts (Pd, Pt, Rh, Ru) supported over alumina have been tested in catalytic WAO (2nd step) at elevated pH to enhance ammonia conversion and organic matter removal, particularly acetic acid. It was found that the catalysts Ru, Pt, and Rh had significant effects on the TOC removal (95.1%, 99.5% and 96.7%, respectively) and on the abatement of ammonia (93.4%, 96.7% and 96.3%, respectively) with high nitrogen selectivity. The catalyst Pd was found to have the less activity while Pt had the best performance. The X-Ray diffraction analysis showed that the support of catalyst was not stable under the experimental conditions since it reacted with phosphate present in solution. Nitrite and nitrate ions were monitored during the oxidation reaction and it was concluded that CWAO of ammonia in real waste treatment framework was in good agreement with the results obtained from the literature for ideal solutions of ammonia.

  4. New Advances in Catalytic Systems for Conversion of CH4 and CO2

    Institute of Scientific and Technical Information of China (English)

    Gengliang Chen

    2002-01-01

    One of the main goals for developing the C1 chemical industry is the direct conversion of methane and carbon dioxide to useful products. To realize this goal, researches on new catalytic systems are being globally focused. The exploration has been evolved from traditional heterogeneous catalysis into homogeneous catalysis. Coordinate complexes, biochemical and bionics, and photo- and electrochemical catalysis have been extensively studied in recent years. Tests in laboratories have verified for the direct conversion of CH4 to CH3OH that single-pass converstion of CH4 can reach over 70% in both Hg(Ⅱ) salt and Pt(Ⅱ) complex systems. The main problem of these systems is the obstacles involving reaction kinetics, so they must be solved before moving to pilot tests. Other catalytic systems discussed in the present article include explorations in the early stage. Among them, features of photo and enzymatic catalyst systems, such as mild reaction conditions, better selectivity and environmentally friendliness have been explored, and these researches are significant both in theory and in practical application.

  5. Blending Influence on the Conversion Efficiency of the Cogasification Process of Corn Stover and Coal

    Directory of Open Access Journals (Sweden)

    Anthony Ike Anukam

    2016-01-01

    Full Text Available Characterizations of biomass and coal were undertaken in order to compare their properties and determine the combustion characteristics of both feedstocks. The study was also intended to establish whether the biomass (corn stover used for this study is a suitable feedstock for blending with coal for the purpose of cogasification based on composition and properties. Proximate and ultimate analyses as well as energy value of both samples including their blends were undertaken and results showed that corn stover is a biomass material well suited for blending with coal for the purpose of cogasification, given its high volatile matter content which was measured and found to be 75.3% and its low ash content of 3.3% including its moderate calorific value of 16.1%. The results of the compositional analyses of both pure and blended samples of corn stover and coal were used to conduct computer simulation of the cogasification processes in order to establish the best blend that would result in optimum cogasification efficiency under standard gasifier operating conditions. The final result of the cogasification simulation process indicated that 90% corn stover/10% coal resulted in a maximum efficiency of about 58% because conversion was efficiently achieved at a temperature that is intermediate to that of coal and corn stover independently.

  6. Time-depth conversion of transient electromagnetic method used in coal mines

    Institute of Scientific and Technical Information of China (English)

    YU Jing-cun; WANG Yang-zhou; LIU Jian; ZENG Xiao-bo

    2008-01-01

    Accuracy of time-depth conversion in data processing of transient electromagnetic prospecting always affects the accurate positioning of water bodies in coal mines. In order to improve the accuracy of time-depth conversion, we established a mathematical model of time-depth conversion for a transient electromagnetic method based on the theory of "double smoke ring effect"of full space transient electromagnetic field transmission. Using a 3-layer as well as a 4-layer geo-electric model for roadway floors,we performed the time-depth conversion of theoretical curves of apparent resistance varying over time. In these curves, the depth corresponding to extreme value points is nearly the same as the depth of a geo-electric model. The position of water body determined by our time-depth conversion method agrees well with the result of borehole drilling, indicating that the established time-depth conversion model can clearly improve the accuracy of spatial positioning of water bodies in coal mines.

  7. Time-depth conversion of transient electromagnetic method used in coal mines

    Energy Technology Data Exchange (ETDEWEB)

    Jing-cun Yu; Yang-zhou Wang; Jian Liu; Xiao-bo Zeng [China University of Mining and Technology, Xuzhou (China). School of Resources and Earth Science

    2008-12-15

    Accuracy of time-depth conversion in data processing of transient electromagnetic prospecting always affects the accurate positioning of water bodies in coal mines. In order to improve the accuracy of time-depth conversion, a mathematical model was established of time-depth conversion for a transient electromagnetic method based on the theory of 'double smoke ring effect' of full space transient electromagnetic field transmission. Using a 3-layer as well as a 4-layer geo-electric model for roadway floors, the time-depth conversion of theoretical curves of apparent resistance varying over time was performed. In these curves, the depth corresponding to extreme value points is nearly the same as the depth of a geo-electric model. The position of water body determined by the time-depth conversion method agrees well with the result of borehole drilling, indicating that the established time-depth conversion model can clearly improve the accuracy of spatial positioning of water bodies in coal mines. 14 refs., 3 figs.

  8. MERCURY OXIDATION PROMOTED BY A SELECTIVE CATALYTIC REDUCTION CATALYST UNDER SIMULATED POWDER RIVER BASIN COAL COMBUSTION CONDITIONS

    Science.gov (United States)

    A bench-scale reactor consisting of a natural gas burner and an electrically heated reactor housing a selective catalytic reduction (SCR) catalyst was constructed for studying elemental mercury oxidation under SCR conditions. A low sulfur Power River Basin (PRB) coal combustion ...

  9. Survey and conceptual flow sheets for coal conversion plant handling-preparation and ash/slag removal operations

    Energy Technology Data Exchange (ETDEWEB)

    Zapp, F.C.; Thomas, O.W.; Silverman, M.D.; Dyslin, D.A.; Holmes, J.M.

    1980-03-01

    This study was undertaken at the request of the Fossil Fuel Processing Division of the Department of Energy. The report includes a compilation of conceptual flow sheets, including major equipment lists, and the results of an availability survey of potential suppliers of equipment associated with the coal and ash/slag operations that will be required by future large coal conversion plant complexes. Conversion plant flow sheet operations and related equipment requirements were based on two representative bituminous coals - Pittsburgh and Kentucky No. 9 - and on nine coal conversion processes. It appears that almost all coal handling and preparation and ash/slag removal equipment covered by this survey, with the exception of some coal comminution equipment, either is on hand or can readily be fabricated to meet coal conversion plant capacity requirements of up to 50,000 short tons per day. Equipment capable of handling even larger capacities can be developed. This approach appears to be unjustified, however, because in many cases a reasonable or optimum number of trains of equipment must be considered when designing a conversion plant complex. The actual number of trains of equipment selected will be influenced by the total requied capacity of the complex, the minimum on-line capacity that can be tolerated in case of equipment failure, reliability of specific equipment types, and the number of reactors and related feed injection stations needed for the specific conversion process.

  10. Kinetics and mechanism of catalytic hydroprocessing of components of coal-derived liquids. Twentieth quarterly report, February 16, 1984-May 15, 1984

    Energy Technology Data Exchange (ETDEWEB)

    Gates, B.C.; Olson, J.H.; Schuit, G.C.A.; Stiles, A.B.; Petrakis, L.

    1984-06-26

    Kinetics data have been determined for the catalytic hydroprocessing of the acidic fractions of a heavy distillate of a liquid derived from Powhatan No. 5 coal. A commercial, sulfided Ni-Mo/..gamma..-Al/sub 2/O/sub 3/ catalyst was used in the experiments, carried out at 350/sup 0/C and 120 atm with the coal liquid fractions dissolved in cyclohexane. The feed and hydrotreated products were analyzed by gas chromatography/mass spectrometry. The data were analyzed with group-type methods for compound classes, and results were also obtained for some individual organooxygen compounds. Catalytic hydroprocessing leads to a large increase in the number of compounds and a shift to lower boiling ranges. The data are broadly consistent with reaction networks determined with pure compounds; the most important reactions include aromatic ring hydrogenation, hydrodeoxygenation, and hydrodemethylation. Pseudo first-order rate constants for conversion of the predominant organooxygen compounds are on the order of 10/sup -4/ L/(g of catalyst.s); the reactivity decreases in the order cyclohexylphenol > dimethylhydroxyindane > tetrahydronaphthol > phenylphenol > 1-naphthol. 12 references, 15 figures, 5 tables.

  11. A Reduced Reaction Scheme for Volatile Nitrogen Conversion in Coal Combustion

    DEFF Research Database (Denmark)

    Pedersen, Lars Saaby; Glarborg, Peter; Dam-Johansen, Kim

    1998-01-01

    In pulverised coal flames, the most important volatile nitrogen component forming NOx is HCN. To be able to model the nitrogen chemistry in coal flames it is necessary to have an adequate model for HCN oxidation. The present work was concerned with developing a model for HCN/NH3/NO conversion based...... that the CO/H-2 chemistry was described adequately, the reduced HCN/NH3/NO model compared very well with the detailed model over a wide range of stoichiometries. Decoupling of the HCN chemistry from the CO/H-2 chemistry resulted in over-prediction of the HCN oxidation rate under fuel rich conditions, but had...... negligible effect on the CO/H-2 chemistry. Comparison with simplified HCN models from the literature revealed significant differences, indicating that these models should be used cautiously in modelling volatile nitrogen conversion....

  12. Coal conversion and biomass conversion: Volume 1: Final report on USAID (Agency for International Development)/GOI (Government of India) Alternate Energy Resources and Development Program

    Energy Technology Data Exchange (ETDEWEB)

    Kulkarni, A.; Saluja, J.

    1987-06-30

    The United States Agency for International Development (AID), in joint collaboration with the Government of India (GOI), supported a research and development program in Alternate Energy Resources during the period March 1983 to June 1987. The primary emphasis of this program was to develop new and advanced coal and biomass conversion technologies for the efficient utilization of coal and biomass feedstocks in India. This final ''summary'' report is divided into two volumes. This Report, Volume I, covers the program overview and coal projects and Volume II summarizes the accomplishments of the biomass projects. The six projects selected in the area of coal were: Evaluation of the Freeboard Performance in a Fluidized-Bed Combustor; Scale-up of AFBC boilers; Rheology, Stability and Combustion of Coal-Water Slurries; Beneficiation of Fine Coal in Dense Medium Cyclones; Hot Gas Cleanup and Separation; and Cold Gas Cleanup and Separation.

  13. First-principles quantum-mechanical investigations: The role of water in catalytic conversion of furfural on Pd(111)

    Science.gov (United States)

    Xue, Wenhua; Borja, Miguel Gonzalez; Resasco, Daniel E.; Wang, Sanwu

    2015-03-01

    In the study of catalytic reactions of biomass, furfural conversion over metal catalysts with the presence of water has attracted wide attention. Recent experiments showed that the proportion of alcohol product from catalytic reactions of furfural conversion with palladium in the presence of water is significantly increased, when compared with other solvent including dioxane, decalin, and ethanol. We investigated the microscopic mechanism of the reactions based on first-principles quantum-mechanical calculations. We particularly identified the important role of water and the liquid/solid interface in furfural conversion. Our results provide atomic-scale details for the catalytic reactions. Supported by DOE (DE-SC0004600). This research used the supercomputer resources at NERSC, of XSEDE, at TACC, and at the Tandy Supercomputing Center.

  14. An alternative synthetic approach for efficient catalytic conversion of syngas to ethanol.

    Science.gov (United States)

    Yue, Hairong; Ma, Xinbin; Gong, Jinlong

    2014-05-20

    Ethanol is an attractive end product and a versatile feedstock because a widespread market exists for its commercial use as a fuel additive or a potential substitute for gasoline. Currently, ethanol is produced primarily by fermentation of biomass-derived sugars, particularly those containing six carbons, but coproducts 5-carbon sugars and lignin remain unusable. Another major process for commercial production of ethanol is hydration of ethylene over solid acidic catalysts, yet not sustainable considering the depletion of fossil fuels. Catalytic conversion of synthetic gas (CO + H2) could produce ethanol in large quantities. However, the direct catalytic conversion of synthetic gas to ethanol remains challenging, and no commercial process exists as of today although the research has been ongoing for the past 90 years, since such the process suffers from low yield and poor selectivity due to slow kinetics of the initial C-C bond formation and fast chain growth of the C2 intermediates. This Account describes recent developments in an alternative approach for the synthesis of ethanol via synthetic gas. This process is an integrated technology consisting of the coupling of CO with methanol to form dimethyl oxalate and the subsequent hydrogenation to yield ethanol. The byproduct of the second step (methanol) can be separated and used in circulation as the feedstock for the coupling step. The coupling reaction of carbon monoxide for producing dimethyl oxalate takes place under moderate reaction conditions with high selectivity (∼95%), which ideally leads to a self-closing, nonwaste, catalytic cycling process. This Account also summarizes the progress on the development of copper-based catalysts for the hydrogenation reaction with remarkable efficiencies and stability. The unique lamellar structure and the cooperative effect between surface Cu(0) and Cu(+) species are responsible for the activity of the catalyst with high yield of ethanol (∼91%). The understanding of

  15. Preconversion processing of bituminous coals: New directions to improved direct catalytic coal liquefaction. Final report, September 20, 1991--September 19, 1993

    Energy Technology Data Exchange (ETDEWEB)

    1993-09-01

    One of the main goals for competitive coal liquefaction is to decrease gas yields to reduce hydrogen consumption. Complexing this element as methane and ethane decreases process efficiently and is less cost effective. To decrease the gas yield and increase the liquid yield, an effective preconversion process has been explored on the basis of the physically associated molecular nature of coal. Activities have been focused on two issues: (1) maximizing the dissolution of associated coal and (2) defining the different reactivity associated with a wide molecular weight distribution. Two-step soaking at 350{degrees}C and 400{degrees}C in a recycle oil was found to be very effective for coal solubilization. No additional chemicals, catalysts, and hydrogen are required for this preconversion process. High-volatile bituminous coals tested before liquefaction showed 80--90% conversion with 50--55% oil yields. New preconversion steps suggested are as follows: (1) dissolution of coal with two-step high-temperature soaking, (2) separation into oil and heavy fractions of dissolved coal with vacuum distillation, and (3) selective liquefaction of the separated heavy fractions under relatively mild conditions. Laboratory scale tests of the proposed procedure mode using a small autoclave showed a 30% increase in the oil yield with a 15--20% decrease in the gas yield. This batch operation projects a substantial reduction in the ultimate cost of coal liquefaction.

  16. One-pot catalytic conversion of cellulose and of woody biomass solids to liquid fuels.

    Science.gov (United States)

    Matson, Theodore D; Barta, Katalin; Iretskii, Alexei V; Ford, Peter C

    2011-09-07

    Efficient methodologies for converting biomass solids to liquid fuels have the potential to reduce dependence on imported petroleum while easing the atmospheric carbon dioxide burden. Here, we report quantitative catalytic conversions of wood and cellulosic solids to liquid and gaseous products in a single stage reactor operating at 300-320 °C and 160-220 bar. Little or no char is formed during this process. The reaction medium is supercritical methanol (sc-MeOH) and the catalyst, a copper-doped porous metal oxide, is composed of earth-abundant materials. The major liquid product is a mixture of C(2)-C(6) aliphatic alcohols and methylated derivatives thereof that are, in principle, suitable for applications as liquid fuels.

  17. Advanced coal conversion process demonstration. Technical progress report for the period July 1, 1995--September 30, 1995

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-05-01

    This report describes the technical progress made on the Advanced Coal Conversion Process (ACCP) Demonstration Project from July 1, 1995 through September 30, 1995. The ACCP Demonstration Project is a US Department of Energy (DOE) Clean Coal Technology Project. This project demonstrates an advanced, thermal, coal upgrading process, coupled with physical cleaning techniques, that is designed to upgrade high-moisture, low-rank coals to a high-quality, low-sulfur fuel, registered as the SynCoal process. The coal is processed through three stages (two heating stages followed by an inert cooling stage) of vibrating fluidized bed reactors that remove chemically bound water, carboxyl groups, and volatile sulfur compounds. After thermal upgrading, the cola is put through a deep-bed stratifier cleaning process to separate the pyrite-rich ash from the coal.

  18. Catalytic conversion of light alkanes phase II. Topical report, January 1990--January 1993

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1998-12-31

    The Topical Report on Phase II of the project entitled, Catalytic Conversion of Light Alkanes reviews work done between January 1, 1990 and September 30, 1992 on the Cooperative Agreement. The mission of this work is to devise a new catalyst which can be used in a simple economic process to convert the light alkanes in natural gas to oxygenate products which can either be used as clean-burning, high octane liquid fuels, as fuel components or as precursors to liquid hydrocarbon transportation fuel. This Topical Report documents our efforts to design, prepare, characterize and test novel catalysts for the mild selective reaction of light hydrocarbons with air or oxygen to produce alcohols directly. These catalysts are designed to form active metal oxo (MO) species and to be uniquely active for the homolytic cleavage of the carbon-hydrogen bonds in light alkanes producing intermediates which can form alcohols. Research on the Cooperative Agreement is divided into three Phases relating to three molecular environments for the active catalytic species that we are trying to generate. In this report we present our work on catalysts which have oxidation-active metals in polyoxoanions (PHASE II).

  19. Selective catalytic conversion of bio-oil over high-silica zeolites.

    Science.gov (United States)

    Widayatno, Wahyu Bambang; Guan, Guoqing; Rizkiana, Jenny; Du, Xiao; Hao, Xiaogang; Zhang, Zhonglin; Abudula, Abuliti

    2015-03-01

    Four high silica zeolites, i.e., HSZ-385, 890, 960, and 990 were utilized for the selective catalytic conversion of bio-oil from Fallopia japonica to certain chemicals in a fixed-bed reactor. The Beta-type HSZ-960 zeolite showed the highest selectivity to hydrocarbons, especially to aromatics as well as PAH compounds with the lowest unwanted chemicals while HSZ-890 showed high selectivity to aromatics. NH3-Temperature Programmed Desorption (TPD) analysis indicated that different amounts of acid sites in different zeolites determined the catalytic activity for the oxygen removal from bio-oil, in which the acid sites at low temperature (LT) region gave more contribution within the utilized temperature region. The reusability test of HSZ-960 showed the stability of hydrocarbons yield at higher temperature due to the significant contribution of coke gasification which assisted further deoxygenation of bio-oil. These results provide a guidance to select suitable zeolite catalysts for the upgrading of bio-oil in a practical process.

  20. Catalytic conversion of light alkanes: Quarterly report, January 1-March 31, 1992

    Energy Technology Data Exchange (ETDEWEB)

    Biscardi, J.; Bowden, P.T.; Durante, V.A.; Ellis, P.E. Jr.; Gray, H.B.; Gorbey, R.G.; Hayes, R.C.; Hodge, J.; Hughes, M.; Langdale, W.A.; Lyons, J.E.; Marcus, B.; Messick, D.; Merrill, R.A.; Moore, F.A.; Myers, H.K. Jr.; Seitzer, W.H.; Shaikh, S.N.; Tsao, W.H.; Wagner, R.W.; Warren, R.W.; Wijesekera, T.P.

    1997-05-01

    The first Quarterly Report of 1992 on the Catalytic Conversion of Light Alkanes reviews the work done between January 1. 1992 and March 31, 1992 on the Cooperative Agreement. The mission of this work is to devise a new catalyst which can be used in a simple economic process to convert the light alkanes in natural gas to oxygenate products which can either be used as clean-burning, high octane liquid fuels, as fuel components or as precursors to liquid hydrocarbon transportation fuel. During the past quarter we have continued to design, prepare, characterize and test novel catalysts for the mild selective reaction of light hydrocarbons with air or oxygen to produce alcohols directly. These catalysts are designed to form active metal oxo (MO) species and to be uniquely active for the homolytic cleavage of the carbon-hydrogen bonds in light alkanes producing intermediates which can form alcohols. We continue to investigate three molecular environments for the active catalytic species that we are trying to generate: electron-deficient porphryinic macrocycles (PHASE I), polyoxometallates (PHASE II), and regular oxidic lattices including zeolites and related structures as well as other molecular surface structures having metal oxo groups (PHASE III).

  1. The effect of temperature on the catalytic conversion of Kraft lignin using near-critical water

    DEFF Research Database (Denmark)

    Nguyen, Thi Dieu Huyen; Maschietti, Marco; Åmand, Lars-Erik

    2014-01-01

    The catalytic conversion of suspended LignoBoost Kraft lignin was performed in near-critical water using ZrO2/K2CO3 as the catalytic system and phenol as the co-solvent and char suppressing agent. The reaction temperature was varied from 290 to 370 C and its effect on the process was investigated...... in a continuous flow (1 kg/h). The yields of water-soluble organics (WSO), bio-oil and char (dry lignin basis) were in the ranges of 5–11%, 69–87% and 16–22%, respectively. The bio-oil, being partially deoxygenated, exhibited higher carbon content and heat value, but lower sulphur content than lignin. The main 1......-ring aromatics (in WSO and diethylether-soluble bio-oil) were anisoles, alkylphenols, catechols and guaiacols. The results show that increasing temperature increases the yield of 1-ring aromatics remarkably, while it increases the formation of char moderately. An increase in the yields of anisoles...

  2. Catalytic conversion of light alkanes. Quarterly progress report, April 1--June 30, 1992

    Energy Technology Data Exchange (ETDEWEB)

    Lyons, J.E.

    1992-06-30

    The second Quarterly Report of 1992 on the Catalytic Conversion of Light Alkanes reviews the work done between April 1, 1992 and June 31, 1992 on the Cooperative Agreement. The mission of this work is to devise a new catalyst which can be used in a simple economic process to convert the light alkanes in natural gas to oxygenate products that can either be used as clean-burning, high octane liquid fuels, as fuel components or as precursors to liquid hydrocarbon uwspomdon fuel. During the past quarter we have continued to design, prepare, characterize and test novel catalysts for the mild selective reaction of light hydrocarbons with air or oxygen to produce alcohols directly. These catalysts are designed to form active metal oxo (MO) species and to be uniquely active for the homolytic cleavage of the carbon-hydrogen bonds in light alkanes producing intermediates which can form alcohols. We continue to investigate three molecular environments for the active catalytic species that we are trying to generate: electron-deficient macrocycles (PHASE I), polyoxometallates (PHASE II), and regular oxidic lattices including zeolites and related structures as well as other molecular surface structures having metal oxo groups (PHASE I).

  3. Conversion of the refractory ammonia and acetic acid in catalytic wet air oxidation of animal byproducts

    Institute of Scientific and Technical Information of China (English)

    Virginie Fontanier; Sofiane Zalouk; Stéphane Barbati

    2011-01-01

    Wet air oxidation (WAO) and catalytic wet air oxidation (CWAO) of slaughtered animal byproducts (ABPs) were investigated.Two step experiment was carried out consisting ofa non-catalysed WAO run followed by a CWAO run at 170-275℃, 20 MPa, and reaction time 180 min.The WAO (1st step) of sample (5 g/L total organic carbon (TOC)) yielded (82.0 ± 4)% TOC removal and (78.4 ± 13.2)%conversion of the initial organic-N into NH4+-N.Four metal catalysts (Pd, Pt, Rh, Ru) supported over alumina have been tested in catalytic WAO (2nd step) at elevated pH to enhance ammonia conversion and organic matter removal, particularly acetic acid.It was found that the catalysts Ru, Pt, and Rh had significant effects on the TOC removal (95.1%, 99.5% and 96.7%, respectively) and on the abatement of ammonia (93.4%, 96.7% and 96.3%, respectively) with high nitrogen selectivity.The catalyst Pd was found to have the less activity while Pt had the best performance.The X-Ray diffraction analysis showed that the support of catalyst was not stable under the experimental conditions since it reacted with phosphate present in solution.Nitrite and nitrate ions were monitored during the oxidation reaction and it was concluded that CWAO of ammonia in real waste treatment framework was in good agreement with the results obtained from the literature for ideal solutions of ammonia.

  4. Advanced treatment of biologically pretreated coal gasification wastewater by a novel integration of heterogeneous catalytic ozonation and biological process.

    Science.gov (United States)

    Zhuang, Haifeng; Han, Hongjun; Jia, Shengyong; Hou, Baolin; Zhao, Qian

    2014-08-01

    Advanced treatment of biologically pretreated coal gasification wastewater (CGW) was investigated employing heterogeneous catalytic ozonation integrated with anoxic moving bed biofilm reactor (ANMBBR) and biological aerated filter (BAF) process. The results indicated that catalytic ozonation with the prepared catalyst (i.e. MnOx/SBAC, sewage sludge was converted into sludge based activated carbon (SBAC) which loaded manganese oxides) significantly enhanced performance of pollutants removal by generated hydroxyl radicals. The effluent of catalytic ozonation process was more biodegradable and less toxic than that in ozonation alone. Meanwhile, ANMBBR-BAF showed efficient capacity of pollutants removal in treatment of the effluent of catalytic ozonation at a shorter reaction time, allowing the discharge limits to be met. Therefore, the integrated process with efficient, economical and sustainable advantages was suitable for advanced treatment of real biologically pretreated CGW.

  5. Systems studies of coal conversion processes using a reference simulator. Quarterly progress report, June 13--September 12, 1976

    Energy Technology Data Exchange (ETDEWEB)

    Reklaitis, G.V.; Woods, J.M.

    1976-09-27

    This project has two principal objectives. The first is to construct a modular computer simulation/design package for coal conversion systems. The second is to use this package to study in a programmatic fashion an array of coal conversion flowsheet alternatives. The computerized package is to be based on bench- and large-scale pilot plant data developed by other organizations under ERDA contracts. It is to have sufficient flexibility to permit the user to incorporate process alternatives and engineering design modifications and is to have the capability for detailed cost estimation and economic evaluation. The Illinois Coal Gasification Group Demonstration Plant based on COED and COGAS development work is the first conversion process to be investigated with the simulation package. Other variations to this flowsheet, which retain the COGAS and COED primary conversion sections will be investigated, as well as several alternatives involving other primary conversion technologies currently under development for ERDA.

  6. Kinetic of Catalytic CO{sub 2} Gasification for Cyprus Coal by Gas-Solid Reaction Model

    Energy Technology Data Exchange (ETDEWEB)

    Hwang, Soon Choel; Lee, Do Kyun; Kim, Sang Kyum; Rhee, Young Woo [Chungnam National University, Daejeon (Korea, Republic of); Lee, Si Hyun [Korea Institute of Energy Research, Daejeon (Korea, Republic of)

    2015-10-15

    In general, the coal gasification has to be operated under high temperature (1300~1400 .deg. C) and pressure (30~40 bar). However, to keep this conditions, it needs unnecessary and excessive energy. In this work, to reduce the temperature of process, alkali catalysts such as K{sub 2}CO{sub 3} and Na{sub 2}CO{sub 3} were added into Cyprus coal. We investigated the kinetic of Cyprus char-CO{sub 2} gasification. To determine the gasification conditions, the coal (with and without catalysts) gasified with fixed variables (catalyst loading, catalytic effects of Na{sub 2}CO{sub 3} and K{sub 2}CO{sub 3}, temperatures) by using TGA. When catalysts are added by physical mixing method into Cyprus coal the reaction rate of coal added 7 wt% Na{sub 2}CO{sub 3} is faster than raw coal for Cyprus char-CO{sub 2} gasification. The activation energy of coal added 7 wt% Na{sub 2}CO{sub 3} was calculated as 63 kJ/mol which was lower than raw char. It indicates that Na{sub 2}CO{sub 3} can improve the reactivity of char-CO{sub 2} gasification.

  7. Measurement and modeling of advanced coal conversion processes, Volume I, Part 1. Final report, September 1986--September 1993

    Energy Technology Data Exchange (ETDEWEB)

    Solomon, P.R.; Serio, M.A.; Hamblen, D.G. [and others

    1995-09-01

    The objective of this program was the development of a predictive capability for the design, scale up, simulation, control and feedstock evaluation in advanced coal conversion devices. The foundation to describe coal specific conversion behavior was AFR`s Functional Group and Devolatilization, Vaporization and Crosslinking (DVC) models, which had been previously developed. The combined FG-DVC model was integrated with BYU`s comprehensive two-dimensional reactor model for combustion and coal gasification, PCGC-2, and a one-dimensional model for fixed-bed gasifiers, FBED-1. Progress utilizing these models is described.

  8. Catalytic conversion of chloromethane to methanol and dimethyl ether over two catalytic beds: a study of acid strength

    Energy Technology Data Exchange (ETDEWEB)

    Fernandes, D.R.; Leite, T.C.M.; Mota, C.J.A. [Universidade Federal do Rio de Janeiro (UFRJ), RJ (Brazil). Inst. de Quimica], e-mail: cmota@iq.ufrj.br

    2010-07-15

    The catalytic hydrolysis of chloromethane to methanol and dimethyl ether (DME) was studied over metal-exchanged Beta and Mordenite zeolites, acidic MCM-22 and SAPO-5. The use of a second catalytic bed with HZSM-5 zeolite increased the selectivity to DME, due to methanol dehydration on the acid sites. The effect was more significant on catalysts presenting medium and weak acid site distribution, showing that dehydration of methanol to DME is accomplished over sites of higher acid strength. (author)

  9. Improvements of instrumental proximate and ultimate analysis of coals and coal conversion products

    Energy Technology Data Exchange (ETDEWEB)

    Selucky, M.L.; Iacchelli, A.; Murray, C.; Lieshout, T. van.

    1982-06-01

    Comparison of proximate analyses obtained using ASTM (American Society for Testing of Materials) methods with those from the Fisher coal analyzer shows that the analyzer gives consistently low moisture and ash values, and high volatile matter values. While the accuracy of moisture and ash determinations can be improved by introducing various instrument and crucible modifications, volatile matter values are less accurate, mainly because of differences in heating rates. However, reproducibility of results is very good and, with modifications, the instrument can be used to advantage for internal purposes, chiefly because of its large sample capacity. In ultimate analysis of coals using the Perkin-Elmer element analyzer, the main problem is that the initial purge gas flushing period after sample introduction partially removes water from the sample. Various methods of sample drying have shown that the best approach is to dry the sample directly in the instrument at the temperature used for moisture determination; with this modification of the analystical cycle, excellent reproducibility and correlation with the ASTM method have been achieved. The proximate and ultimate analysis of samples of extracts and extract residue are impaired by the presence of residual solvent. The samples can contain up to 10% residual solvent which appear as moisture in the proximate analysis. The report describes several ways of removing the solvent so that accurate analysis can be obtained. The foregoing modifications to procedures and equipment have considerably improved both accuracy and reliability of results obtained by instrumental methods. In consequence, considerably more samples can be handled than by using ASTM standard procedures. 4 refs., 1 figs., 19 tabs.

  10. Selective Catalytic Oxidation of Hydrogen Sulfide to Elemental Sulfur from Coal-Derived Fuel Gases

    Energy Technology Data Exchange (ETDEWEB)

    Gardner, Todd H.; Berry, David A.; Lyons, K. David; Beer, Stephen K.; Monahan, Michael J.

    2001-11-06

    The development of low cost, highly efficient, desulfurization technology with integrated sulfur recovery remains a principle barrier issue for Vision 21 integrated gasification combined cycle (IGCC) power generation plants. In this plan, the U. S. Department of Energy will construct ultra-clean, modular, co-production IGCC power plants each with chemical products tailored to meet the demands of specific regional markets. The catalysts employed in these co-production modules, for example water-gas-shift and Fischer-Tropsch catalysts, are readily poisoned by hydrogen sulfide (H{sub 2}S), a sulfur contaminant, present in the coal-derived fuel gases. To prevent poisoning of these catalysts, the removal of H{sub 2}S down to the parts-per-billion level is necessary. Historically, research into the purification of coal-derived fuel gases has focused on dry technologies that offer the prospect of higher combined cycle efficiencies as well as improved thermal integration with co-production modules. Primarily, these concepts rely on a highly selective process separation step to remove low concentrations of H{sub 2}S present in the fuel gases and produce a concentrated stream of sulfur bearing effluent. This effluent must then undergo further processing to be converted to its final form, usually elemental sulfur. Ultimately, desulfurization of coal-derived fuel gases may cost as much as 15% of the total fixed capital investment (Chen et al., 1992). It is, therefore, desirable to develop new technology that can accomplish H{sub 2}S separation and direct conversion to elemental sulfur more efficiently and with a lower initial fixed capital investment.

  11. Microbial conversion of higher hydrocarbons to methane in oil and coal reservoirs

    Energy Technology Data Exchange (ETDEWEB)

    Kruger, Martin; Beckmaann, Sabrina; Siegert, Michael; Grundger, Friederike; Richnow, Hans [Geomicrobiology Group, Federal Institute for Geosciences and Natural Resources (Germany)

    2011-07-01

    In recent years, oil production has increased enormously but almost half of the oil now remaining is heavy/biodegraded and cannot be put into production. There is therefore a need for new technology and for diversification of energy sources. This paper discusses the microbial conversion of higher hydrocarbons to methane in oil and coal reservoirs. The objective of the study is to identify microbial and geochemical controls on methanogenesis in reservoirs. A graph shows the utilization of methane for various purposes in Germany from 1998 to 2007. A degradation process to convert coal to methane is shown using a flow chart. The process for converting oil to methane is also given. Controlling factors include elements such as Fe, nitrogen and sulfur. Atmospheric temperature and reservoir pressure and temperature also play an important role. From the study it can be concluded that isotopes of methane provide exploration tools for reservoir selection and alkanes and aromatic compounds provide enrichment cultures.

  12. PILOT-SCALE STUDY OF THE EFFECT OF SELECTIVE CATALYTIC REDUCTION CATALYST ON MERCURY SPECIATION IN ILLINOIS AND POWDER RIVER BASIN COAL COMBUSTION FLUE GASES

    Science.gov (United States)

    A study was conducted to investigate the effect of selective catalytic reduction (SCR) catalyst on mercury (Hg) speciation in bituminous and subbituminous coal combustion flue gases. Three different Illinois Basin bituminous coals (from high to low sulfur and chlorine) and one Po...

  13. Catalytic Destruction of a Surrogate Organic Hazardous Air Pollutant as a Potential Co-benefit for Coal-fired Selective Catalyst Reduction Systems

    Science.gov (United States)

    Catalytic destruction of benzene (C6H6), a surrogate for organic hazardous air pollutants (HAPs) produced from coal combustion, was investigated using a commercial selective catalytic reduction (SCR) catalyst for evaluating the potential co-benefit of the SCR technology for reduc...

  14. Catalytic Enhancement of Carbon Black and Coal-Fueled Hybrid Direct Carbon Fuel Cells

    DEFF Research Database (Denmark)

    Deleebeeck, Lisa; Ippolito, Davide; Kammer Hansen, Kent

    2015-01-01

    was investigated using current-voltage-power density curves. In the anode chamber, catalysts are mixed with the carbon-carbonate mixture. These catalysts include various manganese oxides (MnO2, Mn2O3, Mn3O4, MnO), metal carbonates (Ag2CO3, MnCO3, Ce2(CO3)3), metals (Ag, Ce, Ni), doped-ceria (CeO2, Ce1-xGdxO2-x/2......, Ce1-xREExO2-δ (REE = Pr, Sm)) and metal oxides (LiMn2O4, Ag2O). Materials showing the highest activity in carbon black (Mn2O3, CeO2, Ce0.6Pr0.4O2-δ, Ag2O) were subsequently tested for catalytic activity toward bituminous coal, as revealed by both I-V-P curves and electrochemical impedance......Hybrid direct carbon fuel cells (HDCFCs) consisting of a solid carbon (carbon black)-molten carbonate ((62–38 wt% Li-K)2CO3) mixtures in the anode chamber of an anode-supported solid oxide fuel cell type full-cell are tested for their electrochemical performance between 700 and 800°C. Performance...

  15. Exxon catalytic coal-gasification process development program. Quarterly technical progress report, October-December 1979

    Energy Technology Data Exchange (ETDEWEB)

    Euker, Jr, C. A.

    1980-03-01

    Work continued on the catalyst recovery screening studies to evaluate the economic impacts of alternative processing approaches and solid-liquid separation techniques. Equipment specifications have been completed for two cases with countercurrent water washing using rotary-drum filters for the solid-liquid separations. Material and energy balances have been completed for an alternative methane recovery process configuration using low pressure stripping which requires 26% less horsepower than the Study Design system. A study has been initiated to identify trace components which might be present in the CCG gas loop and to assess their potential impacts on the CCG process. This information will be used to assist in planning an appropriate series of analyses for the PDU gasifier effluent. A study has been initiated to evaluate the use of a small conventional steam reformer operating in parallel with a preheat furnace for heat input to the catalytic gasifier which avoids the potential problem of carbon laydown. Preliminary replies from ten manufacturers are being evaluated as part of a study to determine the types and performance of coal crushing equipment appropriate for commercial CCG plants. A material and energy balance computer model for the CCG reactor system has been completed. The new model will provide accurate, consistent and cost-efficient material and energy balances for the extensive laboratory guidance and process definition studies planned under the current program. Other activities are described briefly.

  16. The formation mechanism of CO2 and its conversion in the process of coal gasification under arc plasma conditions

    Science.gov (United States)

    He, Xiaojun; Zheng, Mingdong; Qiu, Jieshan; Zhao, Zongbin; Ma, Tengcai

    2006-05-01

    The carbon dioxide (CO2) formation mechanism and co-conversion of CO2 with coal was investigated in the process of coal gasification in a steam medium at atmospheric pressure under arc plasma conditions in a tube-type setup. The arc plasma was diagnosed in situ by optical emission spectroscopy and the gas products were analysed by gas chromatography. CO2 yields are correlated with the quantitative emission peak intensity of the active species in plasma when the operating parameter is changed. The results show that the greater the emission peak intensity of the CH radicals, C2 radicals, OH radicals or O atoms, the smaller the CO2 yield is, which means that the CO2 formation process is inhibited by increasing the concentration of the mentioned active species under arc plasma conditions. On the basis of the diagnosis results, co-conversion of CO2 and coal in a steam medium under plasma conditions was carried out in the same setup and the results show that CO2 conversion reaches 88.6% while the concentration of CO + H2 reaches 87.4%; at the same time, coal conversion is in the range 54.7-68.7%, which proves that co-conversion of CO2 and coal in a steam medium under plasma conditions might be a prospective way to utilize CO2 and the production of synthesis gas.

  17. Postextraction Separation, On-Board Storage, and Catalytic Conversion of Methane in Natural Gas: A Review.

    Science.gov (United States)

    Saha, Dipendu; Grappe, Hippolyte A; Chakraborty, Amlan; Orkoulas, Gerassimos

    2016-10-12

    In today's perspective, natural gas has gained considerable attention, due to its low emission, indigenous availability, and improvement in the extraction technology. Upon extraction, it undergoes several purification protocols including dehydration, sweetening, and inert rejection. Although purification is a commercially established technology, several drawbacks of the current process provide an essential impetus for developing newer separation protocols, most importantly, adsorption and membrane separation. This Review summarizes the needs of natural gas separation, gives an overview of the current technology, and provides a detailed discussion of the progress in research on separation and purification of natural gas including the benefits and drawbacks of each of the processes. The transportation sector is another growing sector of natural gas utilization, and it requires an efficient and safe on-board storage system. Compressed natural gas (CNG) and liquefied natural gas (LNG) are the most common forms in which natural gas can be stored. Adsorbed natural gas (ANG) is an alternate storage system of natural gas, which is advantageous as compared to CNG and LNG in terms of safety and also in terms of temperature and pressure requirements. This Review provides a detailed discussion on ANG along with computation predictions. The catalytic conversion of methane to different useful chemicals including syngas, methanol, formaldehyde, dimethyl ether, heavier hydrocarbons, aromatics, and hydrogen is also reviewed. Finally, direct utilization of methane onto fuel cells is also discussed.

  18. CATALYTIC CONVERSION OF MUNICIPAL WASTE PLASTIC INTO GASOLINE-RANGE PRODUCTS OVER MESOPOROUS MATERIALS

    Institute of Scientific and Technical Information of China (English)

    Jorge Norberto Beltramini

    2006-01-01

    In the last 20 years, it has become apparent that waste produced from plastics was becoming an environmental problem because of their low biodegradability. Though several methods have been proposed for recycling waste plastics, it is generally accepted that material recovery is not a long-term solution to the present problem, and that energy or chemical recovery is a more attractive alternative, including cracking into the monomer constituents, combustion to produce energy, and thermal or catalytic conversion to produce useful intermediate chemicals.This paper is a contribution in the area of the last option for energy recovery. There have been a number of publications reporting the use of molecular sieves and amorphous silica-alumina catalysts for the cracking of polymers into a range of hydrocarbons. The research work reported here demonstrates the ability of mesoporous catalysts in cracking polyethylene into gasoline range products.It was found that for mesoporous MCM-41 catalysts, its cracking activity increases with its crystallinity, displaying higher activity with smaller pore diameters. The hydrocarbon product distribution strongly indicates a carbenium ion cracking mechanism. The product distribution was also compared with those obtained from thermal cracking tests.

  19. Catalytic conversion of light alkanes, Phase 3. Topical report, January 1990--December 1992

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1992-12-31

    The mission of this work is to devise a new catalyst which can be used in the first simple, economic process to convert the light alkanes in natural gas to an alcohol-rich oxygenated product which can either be used as an environmentally friendly, high-performance liquid fuel, or a precursor to a liquid hydrocarbon transportation fuel. The authors have entered the proof-of-concept stage for converting isobutane to tert butyl alcohol in a practical process and are preparing to enter proof-of-concept of a propane to isopropyl alcohol process in the near future. Methane and ethane are more refractory and thus more difficult to oxidize than the C{sub 3} and C{sub 4} hydrocarbons. Nonetheless, advances made in this area indicate that further research progress could achieve the goal of their direct conversion to alcohols. Progress in Phase 3 catalytic vapor phase methane and ethane oxidation over metals in regular oxidic lattices are the subject of this topical report.

  20. Process Design and Economics for the Conversion of Lignocellulosic Biomass to Hydrocarbons: Dilute-Acid and Enzymatic Deconstruction of Biomass to Sugars and Catalytic Conversion of Sugars to Hydrocarbons

    Energy Technology Data Exchange (ETDEWEB)

    Davis, R. [National Renewable Energy Lab. (NREL), Golden, CO (United States); Tao, L. [National Renewable Energy Lab. (NREL), Golden, CO (United States); Scarlata, C. [National Renewable Energy Lab. (NREL), Golden, CO (United States); Tan, E. C. D. [National Renewable Energy Lab. (NREL), Golden, CO (United States); Ross, J. [Harris Group Inc., New York, NY (United States); Lukas, J. [Harris Group Inc., New York, NY (United States); Sexton, D. [Harris Group Inc., New York, NY (United States)

    2015-03-01

    This report describes one potential conversion process to hydrocarbon products by way of catalytic conversion of lignocellulosic-derived hydrolysate. This model leverages expertise established over time in biomass deconstruction and process integration research at NREL, while adding in new technology areas for sugar purification and catalysis. The overarching process design converts biomass to die die diesel- and naphtha-range fuels using dilute-acid pretreatment, enzymatic saccharification, purifications, and catalytic conversion focused on deoxygenating and oligomerizing biomass hydrolysates.

  1. Effect of structure and surface properties on the catalytic activity of nanodiamond in the conversion of 1,2-dichloroethane

    Science.gov (United States)

    Tveritinova, E. A.; Zhitnev, Yu. N.; Kulakova, I. I.; Maslakov, K. I.; Nesterova, E. A.; Kharlanov, A. N.; Ivanov, A. S.; Savilov, S. V.; Lunin, V. V.

    2015-04-01

    The catalytic activity of a detonation nanodiamond and its Ni-containing forms in the conversion of 1,2-dichloroethane is studied and compared with the activity of other carbon and nanocarbon materials: carbon nanotubes, "Dalan" synthetic diamond, and fluorinated graphite. The surface and structure of the carbon materials are characterized using XRD, diffuse reflectance IR spectroscopy, XPS, BET, and TPR. The catalytic properties of the materials are studied using the pulsed microcatalytic method. It is found that the synthetic diamond, the nanodiamond, and its Ni-containing forms are catalysts for dichloroethane conversion in a nitrogen atmosphere, where the main product is ethylene. It is noted that the catalytic activity of deactivated diamond catalysts is restored after hydrogen treatment. It is shown that the carbon structure of the nanodiamond and the "Dalan" synthetic diamond with hydrogen groups located on it plays a key role in the dichloroethane conversion. It is found that the nanodiamond acts simultaneously as a catalyst and an adsorbent of chlorine-containing products of dichloroethane conversion.

  2. Energy conservation in coal conversion. Final report, September 15, 1977--September 1, 1978. Selected case studies and conservation methodologies

    Energy Technology Data Exchange (ETDEWEB)

    Purcupile, J.C.

    1978-09-01

    The purpose of this study is to apply the methodologies developed in the Energy Conservation in Coal Conversion August, 1977 Progress Report - Contract No. EY77S024196 - to an energy efficient, near-term coal conversion process design, and to develop additional, general techniques for studying energy conservation and utilization in coal conversion processes. The process selected for study was the Ralph M. Parsons Company of Pasadena, California ''Oil/Gas Complex, Conceptual Design/Economic Analysis'' as described in R and D Report No. 114 - Interim Report No. 4, published March, 1977, ERDA Contract No. E(49-18)-1975. Thirteen papers representing possible alternative methods of energy conservation or waste heat utilization have been entered individually into EDB and ERA. (LTN)

  3. Soft-chemical synthesis and catalytic activity of Ni-Al and Co-Al layered double hydroxides (LDHs intercalated with anions with different charge density

    Directory of Open Access Journals (Sweden)

    Takahiro Takei

    2014-09-01

    Full Text Available Co-Al and Ni-Al layered double hydroxides (LDHs intercalated with three types of anionic molecules, dodecylsulfate (C12H25SO4−, DS, di-2-ethylsulfosuccinate ([COOC2H3EtBu]2C2H3SO3−, D2ES, and polytungstate (H2W12O4210−, HWO were prepared by means of ion-exchange and co-precipitation processes. With the use of DS and D2ES as intercalation agents, high crystallinity was maintained after intercalation into the LDHs. In the case of HWO, the intercalated LDHs could be obtained by ion-exchange as well as co-precipitation with a decline in the crystallinity; however, unreacted LDH was detected in the ion-exchange samples, and some unwanted phases such as hydroxide and pyrochlore were generated by the co-precipitation process. The maximum specific surface area and pore volume of the Ni-Al sample with intercalated HWO, prepared by the ion-exchange process were 74 m2/g and 0.174 mL/g, respectively. The occupancies of DS, D2ES, and HWO within the interlayer space were approximately 0.3–0.4, 0.5–0.6, and 0.1–0.2, respectively, in the Co-Al and Ni-Al LDHs. Analysis of the catalytic activity demonstrated that the DS-intercalated Ni-Al LDH sample exhibited relatively good catalytic activity for conversion of cyclohexanol to cyclohexanone.

  4. DEVELOPMENT OF HIGH ACTIVITY, COAL DERIVED, PROMOTED CATALYTIC SYSTEMS FOR NOx REDUCTION AT LOW TEMPERATURES

    Energy Technology Data Exchange (ETDEWEB)

    Joseph M. Calo

    1998-12-31

    This project is directed at an investigation of catalytic NO{sub x} reduction mechanisms on coal-derived, activated carbon supports at low temperatures. Promoted carbon systems offer some potentially significant advantages for heterogeneous NO{sub x} reduction. These include: low cost; high activity at low temperatures, which minimizes carbon loss; oxygen resistance; and a support material which can be engineered with respect to porosity, transport and catalyst dispersion characteristics. During the reporting period, the following has been accomplished: (1) A MS-TGA (mass spectrometric-thermogravimetric analysis) apparatus, which is one of the primary instruments that will be used in these studies, has been refurbished and modified to meet the requirements of this project. A NO{sub x} chemiluminescence analyzer (ThermoElectron, Model 10) has been added to the instrument to monitor NO{sub x} concentrations in the feed and product streams. Computer control and data acquisition system has been updated and modified to accommodate the requirements of the specific types of experiments planned. The diffusion pumps used to maintain vacuum for the mass spectrometer system have been replaced with turbomolecular pumps (Varian 300 HT). (2) A packed bed reactor/gas flow system has been assembled for performing reactivity studies. This system employs a Kin-Tek gas calibration/mixing system for varying NO and CO concentrations in the feed gas to the packed bed, a NO{sub x} chemiluminescence analyzer (ThermoElectron, Model 10), and a quadrupole mass spectrometer (Dycor). This system is required for steady-state reactivity studies, as well as mechanistic studies on the effects of NO and CO in the gas phase on intermediate oxygen surface complex populations on the carbon substrates. (3) Work has continued on the application of contrast matching, small angle neutron scattering to the characterization and development of char porosity. Contrast matching with perdeuterated toluene has

  5. Selective homogeneous and heterogeneous catalytic conversion of methanol/dimethyl ether to triptane.

    Science.gov (United States)

    Hazari, Nilay; Iglesia, Enrique; Labinger, Jay A; Simonetti, Dante A

    2012-04-17

    The demand for specific fuels and chemical feed-stocks fluctuates, and as a result, logistical mismatches can occur in the supply of their precursor raw materials such as coal, biomass, crude oil, and methane. To overcome these challenges, industry requires a versatile and robust suite of conversion technologies, many of which are mediated by synthesis gas (CO + H(2)) or methanol/dimethyl ether (DME) intermediates. One such transformation, the conversion of methanol/DME to triptane (2,2,3-trimethylbutane) has spurred particular research interest. Practically, triptane is a high-octane, high-value fuel component, but this transformation also raises fundamental questions: how can such a complex molecule be generated from such a simple precursor with high selectivity? In this Account, we present studies of this reaction carried out in two modes: homogeneously with soluble metal halide catalysts and heterogeneously over solid microporous acid catalysts. Despite their very different compositions, reaction conditions, provenance, and historical scientific context, both processes lead to remarkably similar products and mechanistic interpretations. In both cases, hydrocarbon chains grow by successive methylation in a carbocation-based mechanism. The relative rates of competitive processes-chain growth by methylation, chain termination by hydrogen transfer, isomerization, and cracking-systematically depend upon the structure of the various hydrocarbons produced, strongly favoring the formation of the maximally branched C(7) alkane, triptane. The two catalysts also show parallels in their dependence on acid strength. Stronger acids exhibit higher methanol/DME conversion but also tend to favor chain termination, isomerization, and cracking relative to chain growth, decreasing the preference for triptane. Hence, in both modes, there will be an optimal range: if the acid strength is too low, activity will be poor, but if it is too high, selectivity will be poor. A related

  6. Proceedings of the symposium on assessing the industrial hygiene monitoring needs for the coal conversion and oil shale industries

    Energy Technology Data Exchange (ETDEWEB)

    White, O. Jr. (ed.)

    1979-03-01

    This work was supported by the United States Department of Energy, Division of Biomedical and Environmental Research, Analysis and Assessment Program, through the Safety and Environmental Protection Division at Brookhaven National Laboratory. The symposium program included presentations centering around the themes: Recognition of Occupational Health Monitoring Requirements for the Coal Conversion and Oil Shale Industries and Status of Dosimetry Technology for Occupational Health Monitoring for the Coal Conversion and Oil Shale Industries. Sixteen papers have been entered individually into EDB and ERA; six had been entered previously from other sources. (LTN)

  7. Advanced liquefaction using coal swelling and catalyst dispersion techniques. Volume 2, appendices. Final technical report, October 1, 1991--September 30, 1994

    Energy Technology Data Exchange (ETDEWEB)

    Curtis, C.W. [Auburn Univ., AL (United States); Chander, S. [Pennsylvania State Univ., College Park, PA (United States); Gutterman, C.

    1995-04-01

    Liquefaction experiments were undertaken using subbituminous Black Thunder mine coal to observe the effects of aqueous SO{sub 2} coal beneficiation and the introduction of various coal swelling solvents and catalyst precursors. Aqueous SO{sub 2} beneficiation of Black Thunder coal removed alkali metals and alkaline earth metals, increased the sulfur content and increased the catalytic liquefaction conversion to THF solubles compared to untreated Black Thunder coal. The liquefaction solvent had varying effects on coal conversion, depending upon the type of solvent added. The hydrogen donor solvent, dihydroanthracene, was most effective, while a coal-derived Wilsonville solvent promoted more coal conversion than did relatively inert 1-methylnaphthalene. Swelling of coal with hydrogen bonding solvents tetrahydrofuran (THF), isopropanol, and methanol, prior to reaction resulted in increased noncatalytic conversion of both untreated and SO{sub 2} treated Black Thunder coals, while dimethylsulfoxide (DMSO), which was absorbed more into the coal than any other swelling solvent, was detrimental to coal conversion. Swelling of SO{sub 2} treated coal before liquefaction resulted in the highest coal conversions; however, the untreated coal showed the most improvements in catalytic reactions when swelled in either THF, isopropanol, or methanol prior to liquefaction. The aprotic solvent DMSO was detrimental to coal conversion.

  8. Mechanistic Insights into the Structure-Dependent Selectivity of Catalytic Furfural Conversion on Platinum Catalysts

    Energy Technology Data Exchange (ETDEWEB)

    Cai, Qiuxia; Wang, Jianguo; Wang, Yang-Gang; Mei, Donghai

    2015-11-01

    The effects of structure and size on the selectivity of catalytic furfural conversion over supported Pt catalysts in the presence of hydrogen have been studied using first principles density functional theory (DFT) calculations and microkinetic modeling. Four Pt model systems, i.e., periodic Pt(111), Pt(211) surfaces, as well as small nanoclusters (Pt13 and Pt55) are chosen to represent the terrace, step, and corner sites of Pt nanoparticles. Our DFT results show that the reaction routes for furfural hydrogenation and decarbonylation are strongly dependent on the type of reactive sites, which lead to the different selectivity. On the basis of the size-dependent site distribution rule, we correlate the site distributions as a function of the Pt particle size. Our microkinetic results indicate the critical particle size that controls the furfural selectivity is about 1.0 nm, which is in good agreement with the reported experimental value under reaction conditions. This work was supported by National Basic Research Program of China (973 Program) (2013CB733501) and the National Natural Science Foundation of China (NSFC-21306169, 21176221, 21136001, 21101137 and 91334103). This work was also partially supported by the US Department of Energy (DOE), the Office of Basic Energy Sciences, Division of Chemical Sciences, Geosciences & Biosciences. Pacific Northwest National Laboratory (PNNL) is a multiprogram national laboratory operated for DOE by Battelle. Computing time was granted by the grand challenge of computational catalysis of the William R. Wiley Environmental Molecular Sciences Laboratory (EMSL). EMSL is a national scientific user facility located at Pacific Northwest National Laboratory (PNNL) and sponsored by DOE’s Office of Biological and Environmental Research.

  9. Process and apparatus for conversion of water vapor with coal or hydrocarbon into a product gas

    Energy Technology Data Exchange (ETDEWEB)

    Weirich, W.; Barnert, H.; Oertel, M.; Schulten, R.

    1990-03-27

    A process and apparatus are provided for conversion of steam and hydrocarbon, or steam and coal, into a product gas which contains hydrogen. The conversion rate is augmented by effective extraction and removal of hydrogen as and when hydrogen is generated. Within a reaction vessel wherein the conversion takes place, a chamber for collection of hydrogen is formed by the provision of a hydrogen permeable membrane. The chamber is provided with a hydrogen extraction means and houses a support structure, for example, in the form of a mesh providing structural support to the membrane. The membrane may be of a pleated or corrugated construction, so as to provide an enlarged surface for the membrane to facilitate hydrogen extraction. Also, to further facilitate hydrogen extraction, a hydrogen partial pressure differential is maintained across the membrane, such as, for example, by the counter pressure of an inert gas. A preferred configuration for the apparatus of the invention is a tubular construction which houses generally tubular hydrogen extraction chambers. 5 figs.

  10. A novel approach to highly dispersing catalytic materials in coal for gasification. Final technical report, September 1989--November 1992

    Energy Technology Data Exchange (ETDEWEB)

    Abotsi, G.M.K.; Bota, K.B.

    1992-12-01

    The objectives of this project were to investigate the effects of coal surface charge on the uptake of aqueous soluble metal catalysts from solution and to determine the influence of the interfacial interaction on char reactivity. Another goal is to assess the potential of using potassium carbonate, potassium acetate or their mixtures as catalysts for char gasification. The lower cost and the high catalytic activity of the latter compound will produce economic benefits by reducing the amount of potassium carbonate required for efficient char reactivities on a commercial scale. To minimize the interference of the coals` inherent inorganic materials with the added calcium or potassium, the gasification studies were restricted to the demineralized coals. In a manner similar to the effect of pH on the surface electrochemistry of the coals, the reactivities of the calcium- or potassium-loaded chars in bon dioxide at 800{degree}C were dependent upon the pH at which the catalysts were ion-exchanged onto the coals. For the calcium-containing chars, the reactivities increased in the order: pH 6 > pH 10 > pH 1. In contrast, the variation of the gasification rates with potassium loading pH was: pH 6 {approximately} pH 10 {much_gt} pH 1. However, simultaneous adsorption of the metals at {approximately} pH 1 enhanced char reactivity relative to metals loading at pH 6 or 10. These findings are attributed to the differences in the extent of electrostatic interaction between the calcium or potassium ions and the charged coal surface during catalyst loading from solution.

  11. Systems studies of coal conversion processes using a reference simulator. Quarterly report, December 12, 1976--March 31, 1977

    Energy Technology Data Exchange (ETDEWEB)

    Reklaitis, G.V.; Woods, J.M.; Kayihan, F.; Sood, M.

    1977-04-01

    Progress is reported in the development of a modular computer simulation/design package for coal conversion systems based on bench-scale and large pilot plant data. The initial work is based on COGAS and COED process results. The package should be useful for evaluating various flowsheet alternatives. (LTN)

  12. Computer Simulation Techniques for Molecular Structure of Coal for Advanced Coal Conversion Technology; Sekitan kodo henkan no tameno bunshikozo shimyureshon

    Energy Technology Data Exchange (ETDEWEB)

    Takanohashi, Toshimasa [Energy Resources Dept., Tokyo (Japan). Fundamental Research Div.; Nakamura, Kazuo [Osaka Gas Corp., Osaka (Japan). Fundamental Research Laboratories; Iino, Masashi [Tohoku University, Miyagi (Japan), Institute for Chemical Reaction Science

    1999-02-25

    Coal has complex chemical structure consisting of various bond types and the details are still not well understood. Recently, in addition to improvements of analytical techniques, molecular modeling and simulation techniques by using powerful computers and software have greatly developed and it has become possible to apply them to complex structure such as coal. Knowledge of coal's molecular structure is important for the understanding of various coal properties and reactivities under several conditions. In this paper, a new tool, i.e., molecular modeling technique of coal's macromolecular structure and dynamic simulation of coal properties, is introduced and the future applications of this technique will be outlined. (author)

  13. Laboratory Production of Biofuels and Biochemicals from a Rapeseed Oil through Catalytic Cracking Conversion.

    Science.gov (United States)

    Ng, Siauw H; Shi, Yu; Heshka, Nicole E; Zhang, Yi; Little, Edward

    2016-09-02

    The work is based on a reported study which investigates the processability of canola oil (bio-feed) in the presence of bitumen-derived heavy gas oil (HGO) for production of transportation fuels through a fluid catalytic cracking (FCC) route. Cracking experiments are performed with a fully automated reaction unit at a fixed weight hourly space velocity (WHSV) of 8 hr(-1), 490-530 °C, and catalyst/oil ratios of 4-12 g/g. When a feed is in contact with catalyst in the fluid-bed reactor, cracking takes place generating gaseous, liquid, and solid products. The vapor produced is condensed and collected in a liquid receiver at -15 °C. The non-condensable effluent is first directed to a vessel and is sent, after homogenization, to an on-line gas chromatograph (GC) for refinery gas analysis. The coke deposited on the catalyst is determined in situ by burning the spent catalyst in air at high temperatures. Levels of CO2 are measured quantitatively via an infrared (IR) cell, and are converted to coke yield. Liquid samples in the receivers are analyzed by GC for simulated distillation to determine the amounts in different boiling ranges, i.e., IBP-221 °C (gasoline), 221-343 °C (light cycle oil), and 343 °C+ (heavy cycle oil). Cracking of a feed containing canola oil generates water, which appears at the bottom of a liquid receiver and on its inner wall. Recovery of water on the wall is achieved through washing with methanol followed by Karl Fischer titration for water content. Basic results reported include conversion (the portion of the feed converted to gas and liquid product with a boiling point below 221 °C, coke, and water, if present) and yields of dry gas (H2-C2's, CO, and CO2), liquefied petroleum gas (C3-C4), gasoline, light cycle oil, heavy cycle oil, coke, and water, if present.

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

    Science.gov (United States)

    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.

  15. Exploratory study of coal-conversion chemistry. Quarterly report No. 9, March 20, 1980-June 19, 1980. [Hydroxydiphenylmethane, diphenylether, diphenymethane

    Energy Technology Data Exchange (ETDEWEB)

    McMillen, Donald F.; Ogier, Walter C.

    1980-11-19

    This report describes work accomplished under two tasks: Task A, Mechanism of Cleavage of Key Bond Types Present in Coals, and Task B, Catalysis of Conversion in CO-H/sub 2/O Systems. Under Task A, the very effective catalysis of carbon-carbon bond cleavage by iron oxides in hydroxydiphenylmethane structures has been further characterized. An electron-transfer mechanism offers the most likely explanation of the observations that (1) alumina and silica-alumina surfaces are less active catalysts than Fe/sub 3/O/sub 4/, (2) meta-hydroxydiphenylmethane is almost as subject to catalysis as para-hydroxydiphenylmethane, (3) diphenyl ether is less subject to Fe/sub 3/O/sub 4/ catalysis than diphenylmethane, and (4) ortho-methoxydiphenylmethane exhibits the same susceptibility to Fe/sub 3/O/sub 4/ catalysis as ortho-hydroxydiphenylmethane. Under Task B, this quarter we have completed the survey of possible metal catalysts present in the Hastelloy C autoclave. We have found that coal conversion in CO-H/sub 2/O systems is effective when metal oxides such as MoO/sub 4//sup =/, Cr/sub 2/O/sub 7//sup =/, and MnO/sub 4//sup -/ are used as catalysts, but there is less or no coal conversion with FeCl/sub 3/ or Ni(CH/sub 3/COO)/sub 2/. While studying the fate of the catalyst after the reaction, we have isolated formate in the water-soluble fraction. This important information could help us in studying the role of formate in coal conversion. During this quarter, we have also studied the influence of reaction time and fresh CO on coal conversion in the presence of a catalyst. A striking result of 67% of benzene-soluble materials was obtained with an equivalent of 6000 ppM of Cr as sodium dichromate.

  16. Conversion of chicken feather waste to N-doped carbon nanotubes for the catalytic reduction of 4-nitrophenol.

    Science.gov (United States)

    Gao, Lei; Li, Ran; Sui, Xuelin; Li, Ren; Chen, Changle; Chen, Qianwang

    2014-09-02

    Poultry feather is renewable, inexpensive and abundantly available. It holds great business potentials if poultry feather can be converted into valuable functional materials. Herein, we describe a strategy for the catalytic conversion of chicken feather waste to Ni3S2-carbon coaxial nanofibers (Ni3S2@C) which can be further converted to nitrogen doped carbon nanotubes (N-CNTs). Both Ni3S2@C and N-CNTs exhibit high catalytic activity and good reusability in the reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) by NaBH4 with a first-order rate constant (k) of 0.9 × 10(-3) s(-1) and 2.1 × 10(-3) s(-1), respectively. The catalytic activity of N-CNTs is better than that of N-doped graphene and comparable to commonly used noble metal catalysts. The N content in N-CNTs reaches as high as 6.43%, which is responsible for the excellent catalytic performance. This strategy provides an efficient and low-cost method for the comprehensive utilization of chicken feathers. Moreover, this study provides a new direction for the application of N-CNTs.

  17. Integrated catalytic and electrocatalytic conversion of substituted phenols and diaryl ethers

    Energy Technology Data Exchange (ETDEWEB)

    Song, Yang; Chia, Shao H.; Sanyal, Udishnu; Gutierrez, Oliver Y.; Lercher, Johannes A.

    2016-10-17

    Electrocatalytic hydrogenation and catalytic thermal hydrogenation of substituted phenols and diaryl ethers were studied on carbon-supported Rh. For electrocatalytic and catalytic thermal hydrogen addition reactions, the dominant reaction pathway is hydrogenation to cyclic alcohols and cycloalkyl ethers. The presence of substituting methyl or methoxy groups led to lower rates compared to unsubstituted phenol or diphenyl ether. Methoxy or benzyloxy groups, however, undergo C-O bond cleavage via hydrogenolysis and hydrolysis (minor pathway).

  18. Conversion of Fuel-N to N2O and NOx during Coal Combustion in Combustors of Different Scale

    Institute of Scientific and Technical Information of China (English)

    周昊; 黄燕; 莫桂源; 廖子昱; 岑可法

    2013-01-01

    With focus on investigating the effect of combustor scale on the conversion of fuel-N to NOx and N2O, experiments are carried out in three combustors, including single coal particle combustion test rig, laboratory scale circulating fluidized-bed boiler (CFB) and full scale CFB in this work. For single coal particle combustion, the ma-jority of fuel-N (65%-82%) is released as NOx, while only a little (less than 8%) fuel-N yields N2O. But in labora-tory scale CFB, the conversion of fuel-N to N2O is increases, but the conversion of fuel-N to NOx is quite less than that of single coal particle combustion. This is because much char in CFB can promote the NOx reduction by in-creasing N2O formation. In full scale CFB, both of the conversion of fuel-N to NOx and the conversion of fuel-N to N2O are smaller than laboratory scale CFB.

  19. Experimental and modeling study of the effect of CH(4) and pulverized coal on selective non-catalytic reduction process.

    Science.gov (United States)

    Zhang, Yanwen; Cai, Ningsheng; Yang, Jingbiao; Xu, Bo

    2008-10-01

    The reduction of nitric oxide using ammonia combined with methane and pulverized coal additives has been studied in a drop tube furnace reactor. Simulated flue gas with 1000 ppm NO(x) and 3.4% excess oxygen was generated by cylinder gas. Experiments were performed in the temperature range of 700-1200 degrees C to investigate the effects of additives on the DeNO(x) performance. Subsequently, a kinetic mechanism was modified and validated based on experimental results, and a computational kinetic modeling with CHEMKIN was conducted to analyze the secondary pollutants. For both methane and pulverized coal additives, the temperature window is shifted towards lower temperatures. The appropriate reaction temperature is shifted to about 900 and 800 degrees C, respectively with 1000 ppm methane and 0.051 g min(-1) pulverized lignite coal. The addition of methane and pulverized coal widens the temperature window towards lower temperature suggesting a low temperature application of the process. Furthermore, selective non-catalytic reduction (SNCR) reaction rate is accelerated evidently with additives and the residence time to complete the reaction is shortened distinctly. NO(x) reduction efficiency with 80% is achieved in about 0.3s without additive at 1000 degrees C. However, it is achieved in only about 0.2s with 100 ppm methane as additive, and only 0.07 and 0.05s are needed respectively for the cases of 500 and 1000 ppm methane. The modified kinetic modeling agrees well with the experimental results and reveals additional information about the process. Investigation on the byproducts where NO(2) and N(2)O were analyzed by modeling and the others were investigated by experimental means indicates that emissions would not increase with methane and pulverized coal additions in SNCR process and the efficacious temperature range of SNCR reaction is widened approximately with 100 degrees C.

  20. Characteristics of American coals in relation to their conversion into clean-energy fuels. Final report. [1150 samples of US coals

    Energy Technology Data Exchange (ETDEWEB)

    Spackman, W.; Davis, A.; Walker, P.L.; Lovell, H.L.; Vastola, F.J.; Given, P.H.; Suhr, N.H.; Jenkins, R.G.

    1982-06-01

    To further characterize the Nation's coals, the Penn State Coal Sample Bank and Data Base were expanded to include a total of 1150 coal samples. The Sample Bank includes full-seam channel samples as well as samples of lithotypes, seam benches, and sub-seam sections. To the extent feasible and appropriate basic compositional data were generated for each sample and validated and computerized. These data include: proximate analysis, ultimate analysis, sulfur forms analysis, calorific value, maceral analysis, vitrinite reflectance analysis, ash fusion analysis, free-swelling index determination, Gray-King coke type determination, Hardgrove grindability determination, Vicker's microhardness determination, major and minor element analysis, trace element analysis, and mineral species analysis. During the contract period more than 5000 samples were prepared and distributed. A theoretical and experimental study of the pyrolysis of coal has been completed. The reactivity of chars, produced from all ranks of American coals, has been studied with regard to reactivity to air, CO/sub 2/, H/sub 2/ and steam. Another area research has concerned the catalytic effect of minerals and various cations on the gasification processes. Combustion of chars, low volatile fuels, coal-oil-water-air emulsions and other subjects of research are reported here. The products of this research can be found in 23 DOE Technical Research Reports and 49 published papers. As another mechanism of technology transfer, the results have been conveyed via more than 70 papers presented at a variety of scientific meetings. References to all of these are contained in this report.

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

    Energy Technology Data Exchange (ETDEWEB)

    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.

  2. Preconversion processing of bituminous coals: New directions to improved direct catalytic coal liquefaction. [Effect of preconversion heat soak with coal liquids

    Energy Technology Data Exchange (ETDEWEB)

    1992-07-01

    A study of the high-temperature soaking started in this quarter, following the installation of reactors in the previous quarter. Two high-volatile bituminous coals and three coal liquids, which were identified in the previous report, were used. A cross-linked, three-dimensional macromolecular model has been widely accepted f or the structure of coal, but there is no direct evidence to prove this model. The conventional coal structure model has been recently re-examined by this investigator because of the importance of relatively strong intra- and intermolecular interactions in bituminous coals. It was reasonable to deduce that significant portions were physically associated after a study of multistep extractions, associative equilibria, the irreversibility and the dependence of coal concentration on solvent swelling, and consideration of the monophase concept. Physical dissociation which may be significant above 300{degree}C should be utilized for the treatment before liquefaction. The high-temperature soaking in a recycle oil was proposed to dissociate coal complexes.

  3. Superacid Catalyzed Coal Conversion Chemistry. 1st and 2nd Quarterly Technical Progress Reports, September 1, 1983-March 30, 1984.

    Science.gov (United States)

    Olah, G. A.

    1984-01-01

    In our laboratories we have previously developed a mild coal conversion process. This involves the use of a superacid system consisting of HF and BF{sub 3} in presence of hydrogen and/or a hydrogen donor solvent. In order to understand the chemistry involved in the process of depolymerization of coal by the HF:BF{sub 3}:H{sub 2} system we are carrying out a systematic study of a number of coal model compounds. The model compounds selected for present study have two benzene rings connected with various bridging units such as alkylidene, ether, sulfide etc. From studies so far carried out it appears that high pyridine extractibilities achieved by treating coal at temperature below 100 degrees C results from the cleavage of bridges such as present in bibenzyl, diphenyl methane, dibenzyl ether, dibenzyl sulfide etc. On the other hand the increased cyclohexane extractibility and distillability observed at relatively higher temperatures and hydrogen pressures reflects the hydrogenation and cleavage of the aromatic backbone in coal structure similar to what is seen in the conversion of model compounds such as biphenyl, diphenyl ether, diphenyl sulfide, anthracene, etc.

  4. Investigating the Influence of Mesoporosity in Zeolite Beta on its Catalytic Performance for the Conversion of Methanol to Hydrocarbons

    KAUST Repository

    Liu, Zhaohui

    2015-08-26

    Hierarchically porous zeolite Beta (Beta-MS) synthesized by a soft-templating method contains remarkable intra-crystalline mesoporosity, which reduces the diffusion length in zeolite channels down to several nanometers and alters the distribution of Al among distinct crystallographic sites. When used as a catalyst for the conversion of methanol to hydrocarbons (MTH) at 330 oC, Beta-MS exhibited a 2.7-fold larger conversion capacity, a 2.0-fold faster reaction rate, and a remarkably longer lifetime than conventional zeolite Beta (Beta-C). The superior catalytic performance of Beta-MS is attributed to its hierarchical structure, which offers full accessibility to all catalytic active sites. In contrast, Beta-C was easily deactivated because a layer of coke quickly deposited on the outer surfaces of the catalyst crystals, impeding access to interior active sites. This difference is clearly demonstrated by using electron microscopy combined with electron energy loss spectroscopy to probe the distribution of coke in the deactivated catalysts. At both low and high conversions, ranging from 20% to 100%, Beta-MS gave higher selectivity towards higher aliphatics (C4-C7) but lower ethene selectivity compared to Beta-C. Therefore, we conclude that a hierarchical structure decreases the residence time of methylbenzenes in zeolite micropores, disfavoring the propagation of the aromatic-based catalytic cycle. This conclusion is consistent with a recent report on ZSM-5 and is also strongly supported by our analysis of soluble coke species residing in the catalysts. Moreover, we identified an oxygen-containing compound, 4-methyl-benzaldehyde, in the coke, which has not been observed in the MTH reaction before.  

  5. Coal devolatilization and char conversion under suspension fired conditions in O2/N2 and O2/CO2 atmospheres

    DEFF Research Database (Denmark)

    Jensen, Anker Degn; Brix, Jacob; Jensen, Peter Arendt

    2010-01-01

    was burned at 1573 K and 1673 K a faster conversion was found in N2 suggesting that the lower molecular diffusion coefficient of O2 in CO2 lowers the char conversion rate when external mass transfer influences combustion. The reaction of char with CO2 was not observed to have an influence on char conversion......The aim of the present investigation is to examine differences between O2/N2 and O2/CO2 atmospheres during devolatilization and char conversion of a bituminous coal at conditions covering temperatures between 1173 K and 1673 K and inlet oxygen concentrations between 5 and 28 vol.%. The experiments...... indicates that a shift from air to oxy-fuel combustion does not influence the devolatilization process significantly. Char combustion experiments yielded similar char conversion profiles when N2 was replaced with CO2 under conditions where combustion was primarily controlled by chemical kinetics. When char...

  6. Tracing catalytic conversion on single zeolite crystals in 3D with nonlinear spectromicroscopy

    NARCIS (Netherlands)

    Domke, K.F.; Riemer, T.A.; Rago, G.; Parvulescu, A.N.; Bruijnincx, P.C.A.; Enejder, A.; Weckhuysen, B.M.; Bonn, M.

    2012-01-01

    The cost- and material-efficient development of nextgeneration catalysts would benefit greatly from a molecular-level understanding of the interaction between reagents and catalysts in chemical conversion processes. Here, we trace the conversion of alkene and glycol in single zeolite catalyst partic

  7. Catalytic activity of mono and bimetallic Zn/Cu/MWCNTs catalysts for the thermocatalyzed conversion of methane to hydrogen

    Science.gov (United States)

    Erdelyi, B.; Oriňak, A.; Oriňaková, R.; Lorinčík, J.; Jerigová, M.; Velič, D.; Mičušík, M.; Omastová, M.; Smith, R. M.; Girman, V.

    2017-02-01

    Mono and bimetallic multiwalled carbon nanotubes (MWCNTs) fortified with Cu and Zn metal particles were studied to improve the efficiency of the thermocatalytic conversion of methane to hydrogen. The surface of the catalyst and the dispersion of the metal particles were studied by scanning electron microscopy (SEM), secondary ion mass spectrometry (SIMS) and with energy-dispersive X-ray spectroscopy (EDS). It was confirmed that the metal particles were successfully dispersed on the MWCNT surface and XPS analysis showed that the Zn was oxidised to ZnO at high temperatures. The conversion of methane to hydrogen during the catalytic pyrolysis was studied by pyrolysis gas chromatography using different amounts of catalyst. The best yields of hydrogen were obtained using pyrolysis conditions of 900 °C and 1.2 mg of Zn/Cu/MWCNT catalyst for 1.5 mL of methane.The initial conversion of methane to hydrogen obtained with Zn/Cu/MWCNTs was 49%, which represent a good conversion rate of methane to hydrogen for a non-noble metal catalyst.

  8. Systems studies of coal conversion processes using a reference simulator. Quarterly report, July 1, 1977--September 30, 1977

    Energy Technology Data Exchange (ETDEWEB)

    Reklaitis, G.V.; Sood, M.K.; Raghavan, S.; Overturf, B.W.; Fazzoni, G.F.; Ford, J.R.

    1977-11-01

    The objectives of this study are to develop a conceptual flowsheet of a coal conversion plant which will process Illinois No. 6 coal and will employ the basic processing sequence proposed by the Illinois Coal Gasification Group. The conceptual flowsheet differs from the ICGG proposal in that proprietary or otherwise ill-defined processing steps are replaced with units whose operating data is adequately reported in the open literature and for which satisfactory design models can be formulated. The purpose for formulating this flowsheet is to define a base case conceptual process which will be modelled using both the steady state process simulation package being developed for DOE/FE under our current contract as well as the dynamic simulation library being developed by Lehigh University under a separate contract. Key elements in the process are described.

  9. Selective solvent absorption in coal conversion. Quarterly report, July 1, 1991--September 30, 1991

    Energy Technology Data Exchange (ETDEWEB)

    Larsen, J.W.; Lapucha, A.; Lazarov, L.; Amui, J.

    1992-04-01

    The objectives of this project are: (1) to determine the importance of the presence of added hydrogen donor compounds within the coal in the first stage of direct liquefaction processes; and (2) to determine the composition of the solvent absorbed by and present within the coal in the first stage of direct coal liquefaction.

  10. Pilot plant development of a new catalytic process for improved electrostatic separation of fly-ash in coal fired power plants

    Energy Technology Data Exchange (ETDEWEB)

    Olivares del Valle, J.; Salvador Martinez, L.; Muniz Baum, B.; Cortes Galeano, V. [University of Seville, Seville (Spain). Chemical and Environmental Engineering Dept.

    1996-12-31

    A new catalytic process for flue gas conditioning in pulverized coal fired power plants is outlined. Vanadium and platinum catalysts specifically prepared on ceramic honeycomb monoliths to oxidize SO{sub 2} into SO{sub 3} have been tested and evaluated at pilot scale. 10 refs., 3 figs., 2 tabs.

  11. Monitoring temperatures in coal conversion and combustion processes via ultrasound. [Ultrasonic thermometry proposal

    Energy Technology Data Exchange (ETDEWEB)

    Gopalsami, N.; Raptis, A. C.; Mulcahey, T. P.

    1980-02-01

    A study of the state-of-the-art of instrumentation for monitoring temperatures in coal conversion and combustion systems has been carried out. The instrumentation types studied include Thermocouples, Radiation Pyrometers, and Acoustical Thermometers. The capabilities and limitations of each type are reviewed. The study determined that ultrasonic thermometry has the potential of providing viable instrumentation. Consequently, a feasibility study of the ultrasonic thermometry was undertaken. A mathematical model of a pulse-echo ultrasonic temperature measurement system is developed using linear system theory. The mathematical model lends itself to the adaptation of generalized correlation techniques for the estimation of propagation delays. Computer simulations are made to test the efficacy of the signal processing techniques for noise-free as well as noisy signals. Based on the theoretical study, acoustic techniques to measure temperature in reactors and combustors are feasible. To experimentally verify the technique it is needed (a) to test the available sensor materials at high temperatures under erosive and corrosive conditions and (b) upon the selection of the appropriate sensor material to validate the proposed signal processing technique. The base for the applicability of this technique will be the frequency of operation, which will determine the length of the sensor and the noise background at the frequency of interest. It is, however, believed that the proposed technique will provide reliable estimates under the noise background.

  12. Usage of waste products from thermal recycling of plastics waste in enhanced oil recovery or in-situ coal conversion

    Energy Technology Data Exchange (ETDEWEB)

    Fink, M.; Fink, J.K. [Montanuniversitaet Leoben (Austria)

    1998-09-01

    In this contribution a thermal method for crude oil mobilization and in-situ liquefaction of coal is discussed, which will finally yield more organic material, as which has been put in from plastics waste originally into the process. The conversion product from thermal treatment is pumped down into exhausted crude oil reservoirs, where the hydrogen can degrade the residual high viscous oil to cause it to become more prone to flow so that it can be recovered. Such a process will envision two goals: 1. more organic raw material (as crude oil) will be recovered than is initially put in as waste product. 2. atmospheric pollutants from the conversion plant will be trapped in the reservoir, which simplifies the construction of the plant. An analogous process may be performed with coal seams. Coal seams with their high porosity and large specific surface are believed to be in particular useful to filter atmospheric pollutants. Depending on the type of coal the mobilization of organic material by this process may be in the background. (orig./SR)

  13. Electric Field-Enhanced Catalytic Conversion of Methane: AN Experimental Study on the Effects of Corona Discharge on Methane Reactions

    Science.gov (United States)

    Marafee, Abdulathim M. J.

    The oxidative coupling of methane (OCM) is currently being actively studied for the production of higher hydrocarbons from natural gas. The present study concentrates on the oxidative conversion of methane in a high-pressure (one atmosphere), nonthermal plasma formed by corona discharge. Here, methyl radicals are formed by the reaction of methane with negatively-charged oxygen species created in the corona discharge. The results of methane conversion in the presence of both AC and DC corona discharges revealed that ethane and ethylene product selectivity is affected by electrode polarity, frequency, and oxygen partial pressure in the feed. Higher C_2 yields were obtained with the AC corona. All of the AC corona discharges specified here were initiated at room temperature (i.e., no oven or other heat source used), with temperature increases from 300 to 500^circC due to the exothermic gas discharge and exothermic reaction. A reaction mechanism is presented to explain the observed phenomena. The results suggest that AC and/or DC gas discharge techniques should be further studied for improved economics of methane conversion. The oxidative dehydrogenation of ethane in DC corona discharges was investigated. The atomic oxygen radicals initiated by corona discharges are thought to be active for the OXD of ethane. The selectivity to ethylene is affected by the reaction temperature, the DC applied voltage, voltage polarity, and the C_2H _6/O_2 ratio. The results of this study suggest the corona discharge process to be very efficient and selective in the oxidative dehydrogenation of ethane. The effects of DC corona discharge were examined in the presence of a typical OCM catalyst, Sr/La _2O_3. Experimental investigations have correspondingly been conducted, in which all reactive gases passed through a catalyst bed situated within the corona-induced plasma zone. The methane conversion and C_2 yield increased (with O_2 partial pressure) during the corona-enhanced catalytic

  14. Research progress in calcium catalytic action during coal gasification%煤气化过程中钙催化作用的研究进展

    Institute of Scientific and Technical Information of China (English)

    高美琪; 王玉龙; 李凡

    2015-01-01

    Catalytic gasification of coal has been widely investigated. As a catalyst for coal gasification,calcium has been concerned by many researchers. In this paper,the types of calcium that can play catalyst role in coal gasification are summarized. The mechanism and influencing factors of calcium catalytic coal gasification are discussed. It is pointed out that calcium can accelerate the coal gasification rate more effectively because of the synergistic effect when it is selected to catalyze coal gasification together with other materials. Meanwhile , the research on calcium catalytic coal gasification in the near future is prospected. It is suggested that the mechanism of calcium catalytic coal gasification should be further discussed. It is necessary to develop the catalytic coal gasification technology using limestone or slaked lime mixed with other materials,such as black-liquor.%煤的催化气化在国内外已被广泛研究,Ca 作为一种对煤气化反应具有催化作用的碱土金属催化剂也受到许多研究者的关注。本文总结了可作为煤气化反应催化剂的Ca的类型,论述了Ca催化煤气化反应的机理,分析了影响Ca催化作用的主要因素,指出当Ca与其他物质共同作为煤气化反应的催化剂时,往往可以产生协同效应,更有效地催化煤气化反应的进行。同时提出了今后在Ca催化煤气化反应方面所应进行的研究内容,认为进一步探讨Ca在煤气化反应过程中发生的催化机理,开发使用廉价的石灰石、熟石灰,并且与其他物质,尤其是纸浆黑液共同作为煤气化反应的催化剂很有必要。

  15. Catalytic Conversion of Pinus densiflora Over Mesoporous Catalysts Using Pyrolysis Process.

    Science.gov (United States)

    Joo, Sung Kyun; Lee, In-Gu; Lee, Hyung Won; Chea, Kwang-Seok; Jo, Tae Su; Jung, Sang-Chul; Kim, Sang Chai; Ko, Chang Hyun; Park, Young-Kwon

    2016-02-01

    Catalytic pyrolysis experiments were conducted to investigate the possibility of obtaining valuable chemicals from Pinus densiflora, a native Korean tree species occupying 21.4% of the total area under forests in South Korea. Two representative mesoporous catalysts, Al-MCM-41 and Al-MSU-F, as well as hierarchical mesoporous MFI (Meso-MFI) that has both mesopores and micropores, were used as catalysts. Compared to non-catalytic pyrolysis, catalytic pyrolysis was shown to reduce the fractions of levoglucosan, phenolics, and acids in bio-oil, while increasing the fractions of aromatics, PAHs, and furans. Meso-MFI with strong acid sites showed a high selectivity toward aromatics and PAHs, whereas Al-MCM-41 and Al-MSU-F with weak acid sites exhibited a high selectivity toward furanic compounds. The results of this study indicate that choosing a catalyst with an adequate quantity of acidic sites with the required strength is critical for enhancing the production of desired chemicals from Pinus densiflora.

  16. Investigation of products of low-temperature catalytic hydrogenization of Donbas coals

    Energy Technology Data Exchange (ETDEWEB)

    Osipov, A.M.; Osipov, K.D.; Chernyshova, M.I.; Petrik, G.K.

    1980-11-01

    The relationship of the composition and properties of primary products of low-temperature hydrogenation is presented in relation to the nature of the coal, of catalysts, and of the conditions of hydrogenation. Temperature, the nature of the catalysts and of the type of coal used were directly related to the content of methane, ethane, propane, and CO/sub 2/, and of hydrogen sulphide in the case of brown gaseous coals, as well as the dissolving of hydrogenates and asphaltene content. The structural composition of components dissolved in methylene chloride was determined by proton magnetic resonance. Results of the experiments indicated that lead chloride was the most promising catalyst for low-temperature hydrogenation.

  17. Advanced treatment of biologically pretreated coal gasification wastewater by a novel integration of catalytic ultrasound oxidation and membrane bioreactor.

    Science.gov (United States)

    Jia, Shengyong; Han, Hongjun; Zhuang, Haifeng; Xu, Peng; Hou, Baolin

    2015-01-01

    Laboratorial scale experiments were conducted to investigate a novel system integrating catalytic ultrasound oxidation (CUO) with membrane bioreactor (CUO-MBR) on advanced treatment of biologically pretreated coal gasification wastewater. Results indicated that CUO with catalyst of FeOx/SBAC (sewage sludge based activated carbon (SBAC) which loaded Fe oxides) represented high efficiencies in eliminating TOC as well as improving the biodegradability. The integrated CUO-MBR system with low energy intensity and high frequency was more effective in eliminating COD, BOD5, TOC and reducing transmembrane pressure than either conventional MBR or ultrasound oxidation integrated MBR. The enhanced hydroxyl radical oxidation, facilitation of substrate diffusion and improvement of cell enzyme secretion were the mechanisms for CUO-MBR performance. Therefore, the integrated CUO-MBR was the promising technology for advanced treatment in engineering applications.

  18. Non-catalytic co-gasification of sub-bituminous coal and biomass

    Science.gov (United States)

    Nyendu, Guevara Che

    Fluidization characteristics and co-gasification of pulverized sub-bituminous coal, hybrid poplar wood, corn stover, switchgrass, and their mixtures were investigated. Co-gasification studies were performed over temperature range from 700°C to 900°C in different media (N2, CO2, steam) using a bubbling fluidized bed reactor. In fluidization experiments, pressure drop (Delta P) observed for coal-biomass mixtures was higher than those of single coal and biomass bed materials in the complete fluidization regime. There was no systematic trend observed for minimum fluidization velocity ( Umf) with increasing biomass content. However, porosity at minimum fluidization (εmf) increased with increasing biomass content. Channeling effects were observed in biomass bed materials and coal bed with 40 wt.% and 50 wt.% biomass content at low gas flowrates. The effect of coal pressure overshoot reduced with increasing biomass content. Co-gasification of coal and corn stover mixtures showed minor interactions. Synergetic effects were observed with 10 wt.% corn stover. Coal mixed with corn stover formed agglomerates during co-gasification experiments and the effect was severe with increase in corn stover content and at 900°C. Syngas (H2 + CO) concentrations obtained using CO2 as co-gasification medium were higher (~78 vol.% at 700°C, ~87 vol.% at 800°C, ~93 vol.% at 900°C) than those obtained with N2 medium (~60 vol.% at 700°C, ~65 vol.% at 800°C, ~75 vol.% at 900°C). Experiments involving co-gasification of coal with poplar showed no synergetic effects. Experimental yields were identical to predicted yields. However, synergetic effects were observed on H2 production when steam was used as the co-gasification medium. Additionally, the presence of steam increased H2/CO ratio up to 2.5 with 10 wt.% hybrid poplar content. Overall, char and tar yields decreased with increasing temperature and increasing biomass content, which led to increase in product gas.

  19. Modification of Coal Char-loaded TiO2 by Sulfonation and Alkylsilylation to Enhance Catalytic Activity in Styrene Oxidation with Hydrogen Peroxide as Oxidant

    Directory of Open Access Journals (Sweden)

    Mukhamad Nurhadi

    2017-04-01

    Full Text Available The modified coal char from low-rank coal by sulfonation, titanium impregnation and followed by alkyl silylation possesses high catalytic activity in styrene oxidation. The surface of coal char was undergone several steps as such: modification using concentrated sulfuric acid in the sulfonation process, impregnation of 500 mmol titanium(IV isopropoxide and followed by alkyl silylation of n-octadecyltriclorosilane (OTS. The catalysts were characterized by X-ray diffraction (XRD, IR spectroscopy, nitrogen adsorption, and hydrophobicity. The catalytic activity of the catalysts has been examined in the liquid phase styrene oxidation by using aqueous hydrogen peroxide as oxidant. The catalytic study showed the alkyl silylation could enhance the catalytic activity of Ti-SO3H/CC-600(2.0. High catalytic activity and reusability of the o-Ti-SO3H/CC-600(2.0 were related to the modification of local environment of titanium active sites and the enhancement the hydrophobicity of catalyst particle by alkyl silylation. Copyright © 2017 BCREC GROUP. All rights reserved Received: 24th May 2016; Revised: 11st October 2016; Accepted: 18th October 2016 How to Cite: Nurhadi, M. (2017. Modification of Coal Char-loaded TiO2 by Sulfonation and Alkylsilylation to Enhance Catalytic Activity in Styrene Oxidation with Hydrogen Peroxide as Oxidant. Bulletin of Chemical Reaction Engineering & Catalysis, 12 (1: 55-61 (doi:10.9767/bcrec.12.1.501.55-61 Permalink/DOI: http://dx.doi.org/10.9767/bcrec.12.1.501.55-61

  20. Advanced bioreactor systems for gaseous substrates: Conversion of synthesis gas to liquid fuels and removal of SO{sub x} and NO{sub x} from coal combustion gases

    Energy Technology Data Exchange (ETDEWEB)

    Selvaraj, P.T.; Kaufman, E.N.

    1995-06-01

    The purpose of the proposed research program is the development and demonstration of a new generation of gaseous substrate-based bioreactors for the production of liquid fuels from coal synthesis gas and the removal of NO{sub x} and SO{sub x} species from combustion flue gas. Coal is thermochemically converted to synthesis gas consisting of carbon monoxide, hydrogen, and carbon dioxide. Conventional catalytic upgrading of coal synthesis gas into alcohols or other oxychemicals is subject to several processing problems such as interference of the other constituents in the synthesis gases, strict CO/H{sub 2} ratios required to maintain a particular product distribution and yield, and high processing cost due to the operation at high temperatures and pressures. Recently isolated and identified bacterial strains capable of utilizing CO as a carbon source and coverting CO and H{sub 2} into mixed alcohols offer the potential of performing synthesis gas conversion using biocatalysts. Biocatalytic conversion, though slower than the conventional process, has several advantages such as decreased interference of the other constituents in the synthesis gases, no requirement for strict CO/H{sub 2} ratios, and decreased capital and oeprating costs as the biocatalytic reactions occur at ambient temperatures and pressures.

  1. Potential and challenges of zeolite chemistry in the catalytic conversion of biomass.

    Science.gov (United States)

    Ennaert, Thijs; Van Aelst, Joost; Dijkmans, Jan; De Clercq, Rik; Schutyser, Wouter; Dusselier, Michiel; Verboekend, Danny; Sels, Bert F

    2016-02-01

    Increasing demand for sustainable chemicals and fuels has pushed academia and industry to search for alternative feedstocks replacing crude oil in traditional refineries. As a result, an immense academic attention has focused on the valorisation of biomass (components) and derived intermediates to generate valuable platform chemicals and fuels. Zeolite catalysis plays a distinct role in many of these biomass conversion routes. This contribution emphasizes the progress and potential in zeolite catalysed biomass conversions and relates these to concepts established in existing petrochemical processes. The application of zeolites, equipped with a variety of active sites, in Brønsted acid, Lewis acid, or multifunctional catalysed reactions is discussed and generalised to provide a comprehensive overview. In addition, the feedstock shift from crude oil to biomass involves new challenges in developing fields, like mesoporosity and pore interconnectivity of zeolites and stability of zeolites in liquid phase. Finally, the future challenges and perspectives of zeolites in the processing of biomass conversion are discussed.

  2. Investigation of Coal-biomass Catalytic Gasification using Experiments, Reaction Kinetics and Computational Fluid Dynamics

    Energy Technology Data Exchange (ETDEWEB)

    Battaglia, Francine [Virginia Polytechnic Inst. and State Univ. (Virginia Tech), Blacksburg, VA (United States); Agblevor, Foster [Virginia Polytechnic Inst. and State Univ. (Virginia Tech), Blacksburg, VA (United States); Klein, Michael [Univ. of Delaware, Newark, DE (United States); Sheikhi, Reza [Northeastern Univ., Boston, MA (United States)

    2015-12-31

    A collaborative effort involving experiments, kinetic modeling, and computational fluid dynamics (CFD) was used to understand co-gasification of coal-biomass mixtures. The overall goal of the work was to determine the key reactive properties for coal-biomass mixed fuels. Sub-bituminous coal was mixed with biomass feedstocks to determine the fluidization and gasification characteristics of hybrid poplar wood, switchgrass and corn stover. It was found that corn stover and poplar wood were the best feedstocks to use with coal. The novel approach of this project was the use of a red mud catalyst to improve gasification and lower gasification temperatures. An important results was the reduction of agglomeration of the biomass using the catalyst. An outcome of this work was the characterization of the chemical kinetics and reaction mechanisms of the co-gasification fuels, and the development of a set of models that can be integrated into other modeling environments. The multiphase flow code, MFIX, was used to simulate and predict the hydrodynamics and co-gasification, and results were validated with the experiments. The reaction kinetics modeling was used to develop a smaller set of reactions for tractable CFD calculations that represented the experiments. Finally, an efficient tool was developed, MCHARS, and coupled with MFIX to efficiently simulate the complex reaction kinetics.

  3. Investigation of Coal-biomass Catalytic Gasification using Experiments, Reaction Kinetics and Computational Fluid Dynamics

    Energy Technology Data Exchange (ETDEWEB)

    Battaglia, Francine [Virginia Polytechnic Inst. and State Univ. (Virginia Tech), Blacksburg, VA (United States); Agblevor, Foster [Virginia Polytechnic Inst. and State Univ. (Virginia Tech), Blacksburg, VA (United States); Klein, Michael [Univ. of Delaware, Newark, DE (United States); Sheikhi, Reza [Northeastern Univ., Boston, MA (United States)

    2015-09-30

    A collaborative effort involving experiments, kinetic modeling, and computational fluid dynamics (CFD) was used to understand co-gasification of coal-biomass mixtures. The overall goal of the work was to determine the key reactive properties for coal-biomass mixed fuels. Sub-bituminous coal was mixed with biomass feedstocks to determine the fluidization and gasification characteristics of hybrid poplar wood, switchgrass and corn stover. It was found that corn stover and poplar wood were the best feedstocks to use with coal. The novel approach of this project was the use of a red mud catalyst to improve gasification and lower gasification temperatures. An important results was the reduction of agglomeration of the biomass using the catalyst. An outcome of this work was the characterization of the chemical kinetics and reaction mechanisms of the co-gasification fuels, and the development of a set of models that can be integrated into other modeling environments. The multiphase flow code, MFIX, was used to simulate and predict the hydrodynamics and co-gasification, and results were validated with the experiments. The reaction kinetics modeling was used to develop a smaller set of reactions for tractable CFD calculations that represented the experiments. Finally, an efficient tool was developed, MCHARS, and coupled with MFIX to efficiently simulate the complex reaction kinetics.

  4. Catalytic Hydrothermal Conversion of Wet Biomass Feedstocks and Upgrading – Process Design and Optimization

    DEFF Research Database (Denmark)

    Hoffmann, Jessica; Toor, Saqib; Rosendahl, Lasse

    Liquid biofuels will play a major role for a more sustainable energy system of the future. The CatLiq® process is a 2nd generation biomass conversion process that is based on hydrothermal liquefaction. Hydrothermal liquefaction offers a very efficient and feedstock flexible way of converting...... biomass to bio-oil. Bio-oils from hydrothermal liquefaction are characterised by their high feedstock flexibility. Upgrading of complete bio-oils derived from hydrothermal conversion has not yet been extensively studied. Purpose of this work is to reduce the oxygen content of the bio-oil to improve...

  5. Synergetic and inhibition effects in carbon dioxide gasification of blends of coals and biomass fuels of Indian origin.

    Science.gov (United States)

    Satyam Naidu, V; Aghalayam, P; Jayanti, S

    2016-06-01

    The present study investigates the enhancement of CO2 gasification reactivity of coals due to the presence of catalytic elements in biomass such as K2O, CaO, Na2O and MgO. Co-gasification of three Indian coal chars with two biomass chars has been studied using isothermal thermogravimetric analysis (TGA) in CO2 environment at 900, 1000 and 1100°C. The conversion profiles have been used to establish synergetic or inhibitory effect on coal char reactivity by the presence of catalytic elements in biomass char by comparing the 90% conversion time with and without biomass. It is concluded that both biomasses exhibit synergistic behavior when blended with the three coals with casuarina being more synergetic than empty fruit bunch. Some inhibitory effect has been noted for the high ash coal at the highest temperature with higher 90% conversion time for the blend over pure coal, presumably due to diffusional control of the conversion rate.

  6. Catalytic spectrophotometric determination of trace vanadium in fly ash and coal gangue by Triton X-100 enhancing effect

    Institute of Scientific and Technical Information of China (English)

    XIA Changbin; HUANG Niandong

    2004-01-01

    Trace V(V) catalyzes mightily the decolorization reaction of arsenazo Ⅲ (AsA Ⅲ) by oxidizing with H2O2 in a pH 4.0 HAc-NaAc buffer solution, and the addition of Triton X-100 can further increase the sensitivity of the reaction and its catalytic extent is linear with the content of V(V). A catalytic spectrophotometric procedure for determining trace V(V)was developed. The results show that the maximun absorption of the color solution is at 560 nm and the detection limit of the method for V(V) is 0.014 mg@L-1 Beer's law is obeyed for V(V) in the range of 0.00-0.20 mg.L-1. The recoveries are 99.0%-104.6%, and the relative standard deviations (RSD) are 2.7%-3.7%. Combined with ion-exchange resin, the method has been applied to the determination of trace vanadium in fly ash and coal gangue with satisfactory results.

  7. Effect of selective catalytic reduction (SCR) on fine particle emission from two coal-fired power plants in China

    Science.gov (United States)

    Li, Zhen; Jiang, Jingkun; Ma, Zizhen; Wang, Shuxiao; Duan, Lei

    2015-11-01

    Nitrogen oxides (NOx) emission abatement of coal-fired power plants (CFPPs) requires large-scaled installation of selective catalytic reduction (SCR), which would reduce secondary fine particulate matter (PM2.5) (by reducing nitrate aerosol) in the atmosphere. However, our field measurement of two CFPPs equipped with SCR indicates a significant increase of SO42- and NH4+ emission in primary PM2.5, due to catalytic enhancement of SO2 oxidation to SO3 and introducing of NH3 as reducing agent. The subsequent formation of (NH4)2SO4 or NH4HSO4 aerosol is commonly concentrated in sub-micrometer particulate matter (PM1) with a bimodal pattern. The measurement at the inlet of stack also showed doubled primary PM2.5 emission by SCR operation. This effect should therefore be considered when updating emission inventory of CFPPs. By rough estimation, the enhanced primary PM2.5 emission from CFPPs by SCR operation would offset 12% of the ambient PM2.5 concentration reduction in cities as the benefit of national NOx emission abatement, which should draw attention of policy-makers for air pollution control.

  8. Catalytic conversion of alcohols having at least three carbon atoms to hydrocarbon blendstock

    Energy Technology Data Exchange (ETDEWEB)

    Narula, Chaitanya K.; Davison, Brian H.

    2015-11-13

    A method for producing a hydrocarbon blendstock, the method comprising contacting at least one saturated acyclic alcohol having at least three and up to ten carbon atoms with a metal-loaded zeolite catalyst at a temperature of at least 100°C and up to 550°C, wherein the metal is a positively-charged metal ion, and the metal-loaded zeolite catalyst is catalytically active for converting the alcohol to the hydrocarbon blendstock, wherein the method directly produces a hydrocarbon blendstock having less than 1 vol % ethylene and at least 35 vol % of hydrocarbon compounds containing at least eight carbon atoms.

  9. A Green Protocol for Catalytic Conversion of Epoxides to 1,2-Diacetoxy Esters with Phosphomolybdic Acid Alone or Its Supported on Silica Gel

    Energy Technology Data Exchange (ETDEWEB)

    Zeynizadeh, Behzad; Sadighnia, Leila [Urmia University, Urmia (Iran, Islamic Republic of)

    2010-09-15

    Catalytic conversion of structurally different epoxides to the corresponding 1,2-diacetoxy esters was carried out readily with phosphomolybdic acid alone or its supported on SiO{sub 2}. The reactions were carried out under solvolytic or solvent free conditions within 5-15 min at room temperature. The product 1,2-diacetates were obtained in high to excellent yields. Supporting of phosphomolybdic acid on SiO{sub 2} showed the better catalytic activity than Al{sub 2}O{sub 3}. Conversion of optically pure R-(+)-styrene oxide to S-(+)-1,2-diacetoxy-1-phenylethane was carried with phosphomolybdic acid in high yield and stereospecificity.

  10. Catalytic conversion of light alkanes. Final report, January 1, 1990--October 31, 1994

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1998-12-31

    During the course of the first three years of the Cooperative Agreement (Phase I-III), we uncovered a family of metal perhaloporphyrin complexes which had unprecedented activity for the selective air-oxidation of fight alkanes to alcohols. The reactivity of fight hydrocarbon substrates with air or oxygen was in the order: isobutane>propane>ethane>methane, in accord with their homolytic bond dissociation energies. Isobutane was so reactive that the proof-of concept stage of a process for producing tert-butyl alcohol from isobutane was begun (Phase V). It was proposed that as more active catalytic systems were developed (Phases IV, VI), propane, then ethane and finally methane oxidations will move into this stage (Phases VII through IX). As of this writing, however, the program has been terminated during the later stages of Phases V and VI so that further work is not anticipated. We made excellent progress during 1994 in generating a class of less costly new materials which have the potential for high catalytic activity. New routes were developed for replacing costly perfluorophenyl groups in the meso-position of metalloporphyrin catalysts with far less expensive and lower molecular weight perfluoromethyl groups.

  11. CO{sub 2} photo-catalytic conversion for renewable energy

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Qin-Hui; Han, Wen-Dong; Hong, Yi-Juan; Yu, Jian-Guo [East China Univ. of Science and Technology, Shanghai (China). State Key Lab. of Chemical Engineering

    2010-07-01

    A gas-solid heterogeneous system for selective catalytic photoreduction of CO{sub 2} on Pt/TiO{sub 2} nanotube for renewable energy was discussed. Low dimensional Pt/TiO{sub 2} nanotube photocatalysts are synthesized and characterized with X-ray Diffraction, High-resolution Transmission Electron Microscopy, Photoluminescence, CO pulse Chemisorptions, N{sub 2} adsorption-desorption analysis at 77 K and X-ray Fluorescence spectrometry. The catalytic activity was tested in a fixed-bed photocatalysis reactor with the catalyst coated on the quartz plate with a 1{mu}m thickness film and the CH{sub 4} yield on the Pt/TiO{sub 2} nanotube photocatalysts is more remarkable. It increased with the increase of the UV irradiation time and H{sub 2}O/CO{sub 2} molar ratio, accumulating to about 26.8 {mu} mol.h{sup -1}.g{sub Ti}{sup -1}. (orig.)

  12. Functional carbons and carbon nanohybrids for the catalytic conversion of biomass to renewable chemicals in the condensed phase

    Institute of Scientific and Technical Information of China (English)

    John Matthiesen; Thomas Hoff; Chi Liu; Charles Pueschel; Radhika Rao; Jean-Philippe Tessonnier

    2014-01-01

    The production of chemicals from lignocellulosic biomass provides opportunities to synthesize chemicals with new functionalities and grow a more sustainable chemical industry. However, new challenges emerge as research transitions from petrochemistry to biorenewable chemistry. Com-pared to petrochemisty, the selective conversion of biomass-derived carbohydrates requires most catalytic reactions to take place at low temperatures (<300 °C) and in the condensed phase to pre-vent reactants and products from degrading. The stability of heterogeneous catalysts in liquid water above the normal boiling point represents one of the major challenges to overcome. Herein, we review some of the latest advances in the field with an emphasis on the role of carbon materials and carbon nanohybrids in addressing this challenge.

  13. Functional carbons and carbon nanohybrids for the catalytic conversion of biomass to renewable chemicals in the condensed phase

    Energy Technology Data Exchange (ETDEWEB)

    Matthiesen, John; Hoff, Thomas; Liu, Chi; Pueschel, Charles; Rao, Radhika; Tessonnier, Jean-Philippe

    2014-06-01

    The production of chemicals from lignocellulosic biomass provides opportunities to synthesize chemicals with new functionalities and grow a more sustainable chemical industry. However, new challenges emerge as research transitions from petrochemistry to biorenewable chemistry. Compared to petrochemisty, the selective conversion of biomass-derived carbohydrates requires most catalytic reactions to take place at low temperatures (< 300°C) and in the condensed phase to prevent reactants and products from degrading. The stability of heterogeneous catalysts in liquid water above the normal boiling point represents one of the major challenges to overcome. Herein, we review some of the latest advances in the field with an emphasis on the role of carbon materials and carbon nanohybrids in addressing this challenge.

  14. 贝壳 CaO 催化浑源煤焦气化的研究%Study on the Catalytic Gasification of Hunyuan Coal With Shell CaO

    Institute of Scientific and Technical Information of China (English)

    张晓毅; 贺惠民; 何建

    2016-01-01

    The catalytic effect of catalyst prepared from shell by calcination /carbonation on coal char gasification process was studied. Effect of shell size, calcination time, calcination temperature, carbonation temperature and cycle times on the catalytic performance of the catalyst was analyzed. The results show that,the higher calcination temperature and longer calcination time can decrease the catalytic performance of the catalyst, the higher carbonation temperature can lead to better catalytic performance of catalyst; with increasing of calcination/carbonation times,the catalytic performance of the catalyst decreases. The date error is large due to the solving process of activation energy including two data conversion process. Reaction rate constant can reflect the reactivity of char more accurate.%研究了贝壳经过煅烧/碳酸化后作为催化剂对煤焦气化过程的催化效果。主要分析了贝壳粒径、煅烧时间、煅烧温度、碳酸化温度、循环次数等对催化剂催化性能的影响。主要结论为:较高的煅烧温度和较长的煅烧时间均会降低催化剂的催化性能,较高的碳酸化温度会使催化剂催化性能更好;随着煅烧/碳酸化次数增多,催化剂催化性能下降。由于活化能的求解过程需要经过两次数据转换,误差较大,而用反应速率常数能更为准确地反应出煤焦反应活性。

  15. Pretreated Landfill Gas Conversion Process via a Catalytic Membrane Reactor for Renewable Combined Fuel Cell-Power Generation

    Directory of Open Access Journals (Sweden)

    Zoe Ziaka

    2013-01-01

    Full Text Available A new landfill gas-based reforming catalytic processing system for the conversion of gaseous hydrocarbons, such as incoming methane to hydrogen and carbon oxide mixtures, is described and analyzed. The exit synthesis gas (syn-gas is fed to power effectively high-temperature fuel cells such as SOFC types for combined efficient electricity generation. The current research work is also referred on the description and design aspects of permreactors (permeable reformers carrying the same type of landfill gas-reforming reactions. Membrane reactors is a new technology that can be applied efficiently in such systems. Membrane reactors seem to perform better than the nonmembrane traditional reactors. The aim of this research includes turnkey system and process development for the landfill-based power generation and fuel cell industries. Also, a discussion of the efficient utilization of landfill and waste type resources for combined green-type/renewable power generation with increased processing capacity and efficiency via fuel cell systems is taking place. Moreover, pollution reduction is an additional design consideration in the current catalytic processors fuel cell cycles.

  16. Heterogeneous catalytic ozonation of biologically pretreated Lurgi coal gasification wastewater using sewage sludge based activated carbon supported manganese and ferric oxides as catalysts.

    Science.gov (United States)

    Zhuang, Haifeng; Han, Hongjun; Hou, Baolin; Jia, Shengyong; Zhao, Qian

    2014-08-01

    Sewage sludge of biological wastewater treatment plant was converted into sewage sludge based activated carbon (SBAC) with ZnCl₂ as activation agent, which supported manganese and ferric oxides as catalysts (including SBAC) to improve the performance of ozonation of real biologically pretreated Lurgi coal gasification wastewater. The results indicated catalytic ozonation with the prepared catalysts significantly enhanced performance of pollutants removal and the treated wastewater was more biodegradable and less toxic than that in ozonation alone. On the basis of positive effect of higher pH and significant inhibition of radical scavengers in catalytic ozonation, it was deduced that the enhancement of catalytic activity was responsible for generating hydroxyl radicals and the possible reaction pathway was proposed. Moreover, the prepared catalysts showed superior stability and most of toxic and refractory compounds were eliminated at successive catalytic ozonation runs. Thus, the process with economical, efficient and sustainable advantages was beneficial to engineering application.

  17. Direct conversion of methane to aromatics in a catalytic co-ionic membrane reactor.

    Science.gov (United States)

    Morejudo, S H; Zanón, R; Escolástico, S; Yuste-Tirados, I; Malerød-Fjeld, H; Vestre, P K; Coors, W G; Martínez, A; Norby, T; Serra, J M; Kjølseth, C

    2016-08-01

    Nonoxidative methane dehydroaromatization (MDA: 6CH4 ↔ C6H6 + 9H2) using shape-selective Mo/zeolite catalysts is a key technology for exploitation of stranded natural gas reserves by direct conversion into transportable liquids. However, this reaction faces two major issues: The one-pass conversion is limited by thermodynamics, and the catalyst deactivates quickly through kinetically favored formation of coke. We show that integration of an electrochemical BaZrO3-based membrane exhibiting both proton and oxide ion conductivity into an MDA reactor gives rise to high aromatic yields and improved catalyst stability. These effects originate from the simultaneous extraction of hydrogen and distributed injection of oxide ions along the reactor length. Further, we demonstrate that the electrochemical co-ionic membrane reactor enables high carbon efficiencies (up to 80%) that improve the technoeconomic process viability.

  18. Case studies of a COED-based coal-conversion process. Final report, August 1, 1979-July 15, 1980

    Energy Technology Data Exchange (ETDEWEB)

    Reklaitis, G.V.

    1983-02-01

    The objectives of this project were to investigate the process section models developed under a previous DOE contract into a single modified COED coal-conversion process model; to conduct case studies with selected process section models; and to supplement these studies by developing several additional models. A cyclone coal/char combustor model was developed, implemented and documented. A major program of case studies involving three alternative coal-conversion-process configurations (modified COED, COGAS, and COED) was executed. The COGAS configuration proved superior to the modified COED but was shown to be quite limited in the range of feasible operating conditions. Based on a second-law analysis the COED configuration was the most energy efficient of the three. An oil-vapor-quench-process section model was developed. The key element was a three phase stage-wise absorber with external heat removal and side streams. The model was validated against literature performance data. Comparison of the two quench systems showed them to be comparable in capital cost. Finally, flowsheet models were created of three bulk methanation systems. Suitable base cases were identified for each flowsheet. Extensive experimentation was carried out to speed up integration and to improve recycle convergence calculations. Because of excessive computer charges further case studies were terminated.

  19. Catalytic conversion of Chlorella pyrenoidosa to biofuels in supercritical alcohols over zeolites.

    Science.gov (United States)

    Yang, Le; Ma, Rui; Ma, Zewei; Li, Yongdan

    2016-06-01

    Microalgae have been considered as the feedstock for the third generation biofuels production, given its high lipid content and fast productivity. Herein, a catalytic approach for microalgae liquefaction to biocrude is examined in a temperature range of 250-300°C in methanol and ethanol over zeolites. Higher biocrude yield was achieved in ethanol and at lower temperatures, while better quality biocrude with higher light biocrude ratio and lower average molecular weight (Mw) was favored in methanol and at higher temperatures. Application of zeolites improves the biocrude quality significantly. Among the catalysts, HY shows the strongest acidity and performs the best to produce high quality biocrude. Solid residues have been extensively explored with thermal gravity analysis and elemental analysis. It is reported for the first time that up to 99wt.% of sulfur is deposited in the solid residue at 250°C for both solvents.

  20. Reactors for Catalytic Methanation in the Conversion of Biomass to Synthetic Natural Gas (SNG).

    Science.gov (United States)

    Schildhauer, Tilman J; Biollaz, Serge M A

    2015-01-01

    Production of Synthetic Natural Gas (SNG) from biomass is an important step to decouple the use of bioenergy from the biomass production with respect to both time and place. While anaerobic digestion of wet biomass is a state-of-the art process, wood gasification to producer gas followed by gas cleaning and methanation has only just entered the demonstration scale. Power-to-Gas applications using biogas from biomass fermentation or producer gas from wood gasification as carbon oxide source are under development. Due to the importance of the (catalytic) methanation step in the production of SNG from dry biomass or within Power-to-Gas applications, the specific challenges of this step and the developed reactor types are discussed in this review.

  1. Integrated process for the catalytic conversion of biomass-derived syngas into transportation fuels

    Energy Technology Data Exchange (ETDEWEB)

    Dagle, Vanessa Lebarbier; Smith, Colin; Flake, Matthew; Albrecht, Karl O.; Gray, Michel J.; Ramasamy, Karthikeyan K.; Dagle, Robert A.

    2016-01-01

    Efficient synthesis of renewable fuels that will enable cost competitiveness with petroleum-derived fuels remains a grand challenge for U.S. scientists. In this paper, we report on an integrated catalytic approach for producing transportation fuels from biomass-derived syngas. The composition of the resulting hydrocarbon fuel can be modulated to meet specified requirements. Biomass-derived syngas is first converted over an Rh-based catalyst into a complex aqueous mixture of condensable C2+ oxygenated compounds (predominantly ethanol, acetic acid, acetaldehyde, ethyl acetate). This multi-component aqueous mixture then is fed to a second reactor loaded with a ZnxZryOz mixed oxide catalyst, which has tailored acid-base sites, to produce an olefin mixture rich in isobutene. The olefins then are oligomerized using a solid acid catalyst (e.g., Amberlyst-36) to form condensable olefins with molecular weights that can be targeted for gasoline, jet, and/or diesel fuel applications. The product rich in long-chain olefins (C7+) is finally sent to a fourth reactor that is needed for hydrogenation of the olefins into paraffin fuels. Simulated distillation of the hydrotreated oligomerized liquid product indicates that ~75% of the hydrocarbons present are in the jet-fuel range. Process optimization for the oligomerization step could further improve yield to the jet-fuel range. All of these catalytic steps have been demonstrated in sequence, thus providing proof-of-concept for a new integrated process for the production of drop-in biofuels. This unique and flexible process does not require external hydrogen and also could be applied to non-syngas derived feedstock, such as fermentation products (e.g., ethanol, acetic acid, etc.), other oxygenates, and mixtures thereof containing alcohols, acids, aldehydes and/or esters.

  2. Advanced coal conversion process demonstration. Technical progress report, April 1--June 30, 1996

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-10-01

    This project demonstrates an advanced, thermal, coal upgrading process, coupled with physical cleaning techniques, that is designed to upgrade high moisture, low rank coals to a high quality, low sulfur fuel, registered as the SynCoal{reg_sign} process. The coal is processed through three stages (two heating stages followed by an inert cooling stage) of vibrating fluidized bed reactors that remove chemically bound water, carboxyl groups, and volatile sulfur compounds. After thermal upgrading, the coal is put through a deep bed stratifier cleaning process to separate the pyrite rich ash from the coal. The SynCoal process enhances low rank, western coals, usually with a moisture content of 25 to 55 percent, sulfur content of 0.5 to 1.5 percent, and heating value of 5,500 to 9,000 Btu/lb, by producing a stable, upgraded, coal product with a moisture content as low as 1 percent, sulfur content as low as 0.3 percent, and heating value up to 12,000 Btu/lb. The 45 ton per hour unit is located adjacent to a unit train load out facility at Western Energy Company`s Rosebud coal mine near Colstrip, Montana. The demonstration plant is sized at about one-tenth the projected throughput of a multiple processing train commercial facility. During this report period the primary focus has been to continue the operation of the demonstration facility. Production has been going to area power plants. Modifications and maintenance work was also performed this quarter.

  3. Catalytic conversion of palm oil over mesoporous aluminosilicate MCM-41 for the production of liquid hydrocarbon fuels

    Energy Technology Data Exchange (ETDEWEB)

    Twaiq, Farouq A.; Mohamed, Abdul Rahman; Bhatia, Subhash [School of Chemical Engineering, Engineering Campus, Universiti Sains Malaysia, 14300 Nibong Tebal, SPS, Pinang (Malaysia); Zabidi, Noor Asmawati M. [Universiti Teknologi Petronas, Sri Iskandar, 31750 Tronoh, Perak (Malaysia)

    2003-11-15

    The catalytic cracking of palm oil to liquid hydrocarbon fuels was studied in a fixed bed micro-reactor operated at atmospheric pressure, reaction temperature of 723 K and weight hourly space velocity (WHSV) of 2.5 h{sup -1} over the synthesized mesoporous molecular sieve MCM-41 materials. Mesoporous aluminosilicate with Si/Al ratio of 50 was synthesized using the hydrothermal method. Different pore sizes were obtained by changing the type of template and organic directing agent (ODA) used. The synthesized materials were characterized using various analytical methods such as X-ray powder diffraction (XRD), BET surface area, inductive coupled plasma (ICP), MAS NMR, FTIR and temperature-programmed desorption (TPD). The materials exhibit a crystalline structure of MCM-41 mesoporous molecular sieves with surface area varying from 550 to 1200 m{sup 2}/g and an average pore size (APS) ranging from 1.8 to 2.8 nm. The synthesized MCM-41 catalysts show high activity for palm oil cracking. The conversion of palm kernel oil, lower-molecular-weight oil, was higher as compared to higher-molecular-weight, palm olein oil. MCM-41 materials were selective for the formation of linear hydrocarbons, particularly, C{sub 13} when palm kernel oil was used and C{sub 17} when palm olein oil was fed. The yield of liquid product decreased with the increase of surface area of the catalyst. The gasoline selectivity increased whereas diesel selectivity decreased with the conversion of palm oil.

  4. Effect of Sulfation on Zirconia-Pillared Montmorillonite to the Catalytic Activity in Microwave-Assisted Citronellal Conversion

    Directory of Open Access Journals (Sweden)

    Is Fatimah

    2014-01-01

    Full Text Available Preparation of sulfated zirconia-pillared montmorillonite was carried out in two steps; zirconia pillarization and sulfation to zirconia-pillared montmorillonite. The prepared materials were characterized by using X-ray diffraction (XRD, measurement of the specific surface area, total pore volume and pore size distribution by the N2 adsorption method, scanning electron microscopy-energy dispersive X-ray (SEM-EDX, and surface acidity determination by using pyridine adsorption-FTIR analysis. The activity of the materials as catalysts was evaluated for a microwave-assisted conversion of citronellal. The results showed that the prepared materials had a physicochemical character that promoted high catalytic activity to convert citronellal. From varied Zr content and study of the effect of sulfation on the activity, it was found that Zr content and sulfation increase the surface acidity of the material as shown by the higher total conversion and tendency to produce menthol as a product of the tandem cyclization-hydrogenation mechanism.

  5. Catalytic conversion of biomass-derived feedstocks into olefins and aromatics with ZSM-5: the hydrogen to carbon effective ratio

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Huiyan; Cheng, Yu-Ting; Vispute, Tushar; Xiao, R; Huber, George W.

    2011-01-01

    Catalytic conversion of ten biomass-derived feedstocks, i.e.glucose, sorbitol, glycerol, tetrahydrofuran, methanol and different hydrogenated bio-oil fractions, with different hydrogen to carbon effective (H/C{sub eff}) ratios was conducted in a gas-phase flow fixed-bed reactor with a ZSM-5 catalyst. The aromatic + olefin yield increases and the coke yield decreases with increasing H/C{sub eff} ratio of the feed. There is an inflection point at a H/C{sub eff} ratio = 1.2, where the aromatic + olefin yield does not increase as rapidly as it does prior to this point. The ratio of olefins to aromatics also increases with increasing H/C{sub eff} ratio. CO and CO₂ yields go through a maximum with increasing H/C{sub eff} ratio. The deactivation rate of the catalyst decreases significantly with increasing H/C{sub eff} ratio. Coke was formed from both homogeneous and heterogeneous reactions. Thermogravimetric analysis (TGA) for the ten feedstocks showed that the formation of coke from homogeneous reactions decreases with increasing H/C{sub eff} ratio. Feedstocks with a H/C{sub eff} ratio less than 0.15 produce large amounts of undesired coke (more than 12 wt%) from homogeneous decomposition reactions. This paper shows that the conversion of biomass-derived feedstocks into aromatics and olefins using zeolite catalysts can be explained by the H/C{sub eff} ratio of the feed.

  6. Effects of low-temperature catalytic pretreatments on coal structure and reactivity in liquefaction. Technical progress report, October 1993--December 1993

    Energy Technology Data Exchange (ETDEWEB)

    Song, C.; Huang, L.; Wenzel, K.A.; Hatcher, P.G.; Schobert, H.H.

    1994-02-01

    In this quarter, progress has been made in the following two aspects: The influences of temperature, dispersed Mo catalyst, and solvent on the liquefaction conversion and composition of products from low-rank coals; and the hydrous pyrolysis of a lignite and spectroscopic characterization of its structural transformation during the hydrous pyrolysis. The analytical work described in this quarter also represents molecular-level characterization of products. The purpose of the first part of the work described in this quarter is to study the influences of temperature, solvent and dispersed Mo catalyst on the liquefaction conversion and chemical composition of the products. Many specialty chemicals, including one- to four-ring aromatics, could potentially be produced by liquefying coal. To achieve this goal, not only a high coal conversion but also a desirable product distribution is necessary. Therefore, it is of great importance to understand the structural changes of the coal during reaction and to investigate the conditions under which the aliphatics or aromatics can be removed from the macromolecular structure of coal. This quarterly report also describes the hydrous pyrolysis of Potapsco lignite and spectroscopic characterization of its structural transformation during the hydrous pyrolysis. This work has some implications both on the structural changes of low-rank coals during pretreatment and on the geochemical reactions during coalification stage. Vitrinite, a major component of most coals, is derived from degraded wood in ancient peat swamps. Organic geochemical studies conducted on a series of coalified wood samples derived mostly from gymnosperms have allowed the development of a chemical reaction series to characterize the major coalification reactions which lignin, the major coal-producing component of wood, undergoes.

  7. Research and development of rapid hydrogenation for coal conversion to synthetic motor fuels (riser cracking of coal). Final report, April 1, 1976-September 30, 1980

    Energy Technology Data Exchange (ETDEWEB)

    Duncan, D. A.; Beeson, J. L.; Oberle, R. D.

    1981-02-01

    The objective of the program described was to develop a noncatalytic process for the hydropyrolysis of lignite and coal to produce high-octane blending gasoline constituents, methane, ethane, and carbon oxides. The process would operate in a balanced plant mode, using spent char to generate process hydrogen by steam-oxygen gasification. The technical program included the construction and operating of a bench-scale unit (5-10 lb/hr), the design, construction, and operation of a process development unit (PDU) (100 lb/hr), and a final technical and economic assessment of the process, called Riser Cracking of Coal. In the bench-scale unit program, 143 runs were made investigating the effects of pressure, temperature, heating rate, residence time, and particle size, processing North Dakota lignite in hydrogen. Some runs were made in which the hydrogen was preheated to pyrolysis temperatures prior to contact with the coal, and, also, in which steam was substituted for half of the hydrogen. Attempts to operate the bench-scale unit at 1200 psig and 1475/sup 0/F were not successful. Depth of carbon conversion was found to be influenced by hydrogen pressure, hydrogen-to-coal ratio, and the severity of the thermal treatment. The composition of hydrocarbon liquids produced was found to change with severity. At low severity, the liquids contained sizable fractions of phenols and cresols. At high severity, the fraction of phenols and cresols was much reduced, with an attendant increase in BTX. In operating the PDU, it was necessary to use more oxygen than was planned to achieve pyrolysis temperatures because of heat losses, and portions of hydrocarbon products were lost through combustion with a large increase in carbon oxide yields. Economic studies, however, showed that selling prices for gasoline blending stock, fuel oil, and fuel gas are competitive in current markets, so that the process is held to warrant further development.

  8. Wabash Valley Integrated Gasification Combined Cycle, Coal to Fischer Tropsch Jet Fuel Conversion Study

    Energy Technology Data Exchange (ETDEWEB)

    Shah, Jayesh [Lummus Technology Inc., Bloomfield, NJ (United States); Hess, Fernando [Lummus Technology Inc., Bloomfield, NJ (United States); Horzen, Wessel van [Lummus Technology Inc., Bloomfield, NJ (United States); Williams, Daniel [Lummus Technology Inc., Bloomfield, NJ (United States); Peevor, Andy [JM Davy, London (United Kingdom); Dyer, Andy [JM Davy, London (United Kingdom); Frankel, Louis [Canonsburgh, PA (United States)

    2016-06-01

    This reports examines the feasibility of converting the existing Wabash Integrated Gasification Combined Cycle (IGCC) plant into a liquid fuel facility, with the goal of maximizing jet fuel production. The fuels produced are required to be in compliance with Section 526 of the Energy Independence and Security Act of 2007 (EISA 2007 §526) lifecycle greenhouse gas (GHG) emissions requirements, so lifecycle GHG emissions from the fuel must be equal to or better than conventional fuels. Retrofitting an existing gasification facility reduces the technical risk and capital costs associated with a coal to liquids project, leading to a higher probability of implementation and more competitive liquid fuel prices. The existing combustion turbine will continue to operate on low cost natural gas and low carbon fuel gas from the gasification facility. The gasification technology utilized at Wabash is the E-Gas™ Technology and has been in commercial operation since 1995. In order to minimize capital costs, the study maximizes reuse of existing equipment with minimal modifications. Plant data and process models were used to develop process data for downstream units. Process modeling was utilized for the syngas conditioning, acid gas removal, CO2 compression and utility units. Syngas conversion to Fischer Tropsch (FT) liquids and upgrading of the liquids was modeled and designed by Johnson Matthey Davy Technologies (JM Davy). In order to maintain the GHG emission profile below that of conventional fuels, the CO2 from the process must be captured and exported for sequestration or enhanced oil recovery. In addition the power utilized for the plant’s auxiliary loads had to be supplied by a low carbon fuel source. Since the process produces a fuel gas with sufficient energy content to power the plant’s loads, this fuel gas was converted to hydrogen and exported to the existing gas turbine for low carbon power production. Utilizing low carbon fuel gas and

  9. Enhanced catalytic performance of zeolite ZSM-5 for conversion of methanol to dimethyl ether by combining alkaline treatment and partial activation

    NARCIS (Netherlands)

    Wei, Ying; de Jongh, Petra E.; Bonati, Matteo L. M.; Law, David J.; Sunley, Glenn J.; de Jong, Krijn P.

    2015-01-01

    Zeolite ZSM-5 (MFI) due to its excellent hydrothermal stability and high catalytic activity for methanol dehydration to dimethyl ether (MID) has been considered for use in combination with a methanol synthesis catalyst, such as Cu/ZnO/Al2O3, in the conversion of syngas to dimethyl ether. However, th

  10. Innovative clean coal technology (ICCT): Demonstration of selective catalytic reduction (SCR) technology for the control of nitrogen oxide (NO{sub x}) emissions from high-sulfur coal-fired boilers. Quarterly report No. 3, January--March 1991

    Energy Technology Data Exchange (ETDEWEB)

    1991-07-01

    The objective of this project is to demonstrate and evaluate commercially available Selective Catalytic Reduction (SCR) catalysts from US, Japanese and European catalyst suppliers on a high-sulfur US coal-fired boiler. SCR is a post-combustion nitrogen oxide (NOx) control technology that involves injecting ammonia into the flue gas generated from coal combustion in an electric utility boiler. The flue gas containing ammonia is then passed through a reactor that contains a specialized catalyst. In the presence of the catalyst, the ammonia reacts with NOx to convert it to nitrogen and water vapor.

  11. Innovative clean coal technology (ICCT): Demonstration of selective catalytic reduction (SCR) technology for the control of nitrogen oxide (NO sub x ) emissions from high-sulfur coal-fired boilers

    Energy Technology Data Exchange (ETDEWEB)

    1991-07-01

    The objective of this project is to demonstrate and evaluate commercially available Selective Catalytic Reduction (SCR) catalysts from US, Japanese and European catalyst suppliers on a high-sulfur US coal-fired boiler. SCR is a post-combustion nitrogen oxide (NOx) control technology that involves injecting ammonia into the flue gas generated from coal combustion in an electric utility boiler. The flue gas containing ammonia is then passed through a reactor that contains a specialized catalyst. In the presence of the catalyst, the ammonia reacts with NOx to convert it to nitrogen and water vapor.

  12. Innovative Clean Coal Technology (ICCT). Demonstration of Selective Catalytic Reduction (SCR) technology for the control of Nitrogen Oxide (NO{sub x}) emissions from high-sulfur coal-fired boilers. Technical progress report, third and fourth quarters 1995

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-05-01

    The objective of this project is to demonstrate and evaluate commercially available Selective Catalytic Reduction (SCR) catalysts from U.S., Japanese, and European catalyst suppliers on a high-sulfur U.S. coal-fired boiler. SCR is a post-combustion nitrogen oxide (NO{sub x}) control technology that involves injecting ammonia into the flue gas generated from coal combustion in an electric utility boiler. The flue gas containing ammonia is then passed through a reactor that contains a specialized catalyst. In the presence of the catalyst, the ammonia reacts with NO{sub x} to convert it to nitrogen and water vapor.

  13. Innovative Clean Coal Technology (ICCT): Demonstration of Selective Catalytic Reduction (SCR) technology for the control of nitrogen oxide (NO sub x ) emissions from high-sulfur coal-fired boilers

    Energy Technology Data Exchange (ETDEWEB)

    1991-02-01

    The objective of this project is to demonstrate and evaluate commercially available Selective Catalytic Reduction (SCR) catalysts from US, Japanese and European catalyst suppliers on a high-sulfur US coal-fired boiler. SCR is a post-combustion nitrogen oxide NO{sub x} control technology that involves injecting ammonia into the flue gas generated from coal combustion in an electric utility boiler. The flue gas containing ammonia is then passed through a reactor that contains a specialized catalyst. In the presence of the catalyst, the ammonia reacts with NO{sub x} to convert it to nitrogen and water vapor.

  14. Innovative Clean Coal Technology (ICCT): Demonstration of Selective Catalytic Reduction (SCR) technology for the control of nitrogen oxide (NO{sub x}) emissions from high-sulfur coal-fired boilers. Quarterly report No. 2, October--December 1990

    Energy Technology Data Exchange (ETDEWEB)

    1991-02-01

    The objective of this project is to demonstrate and evaluate commercially available Selective Catalytic Reduction (SCR) catalysts from US, Japanese and European catalyst suppliers on a high-sulfur US coal-fired boiler. SCR is a post-combustion nitrogen oxide NO{sub x} control technology that involves injecting ammonia into the flue gas generated from coal combustion in an electric utility boiler. The flue gas containing ammonia is then passed through a reactor that contains a specialized catalyst. In the presence of the catalyst, the ammonia reacts with NO{sub x} to convert it to nitrogen and water vapor.

  15. Catalytic conversion of γ-valerolactone to ε-caprolactam: towards nylon from renewable feedstock.

    Science.gov (United States)

    Raoufmoghaddam, Saeed; Rood, Marcus T M; Buijze, Florine K W; Drent, Eite; Bouwman, Elisabeth

    2014-07-01

    The conversion of γ-valerolactone (GVL) in three atom-efficient steps to the important polymer precursor ε-caprolactam is reported. The bio-based GVL can be converted to a mixture of isomeric methyl pentenoates (MP) via trans-esterification with methanol with 94% yield (ratio of 3-MP/4-MP=3:1); subsequent aminolysis with ammonia leads to a mixture of pentenamides (PA) almost quantitatively (99% conversion). The resulting pentenamides are ultimately converted into ε-caprolactam via a rhodium-catalyzed intramolecular hydroamidomethylation reaction, comprising an initial hydroformylation of the alkene moiety of PA and subsequent ring-closing reductive amidation of the resulting aldehyde with the amide functionality. A promising yield of caprolactam of about 90% can be obtained with a Rh/xantphos catalyst system in a two-stage hydroformylation-reductive amidation using pure 4-PA as feedstock. The use of 3-PA as a substrate not only results in a significantly lower regioselectivity for the 7-membered lactam, but also in the formation of high amounts of valeramide (VA). Consequently, a best overall yield of caprolactam of nearly 40% could be demonstrated with a Rh/POP-xantphos [POP-xantphos=4,5-bis(2,8-dimethyl-10-phenoxaphosphino)-9,9,-dimethylxanthene] catalyst system based on the 3:1 mixture of 3-PA/4-PA directly obtainable from GVL.

  16. Catalytic conversion of alcohols--11. Influence of preparation and pretreatment on the selectivity of zirconia

    Energy Technology Data Exchange (ETDEWEB)

    Davis, B.H. (Potomac State Coll. W. Va. Univ.); Ganesan, P.

    1979-09-01

    Conversion of 2-butanol, 2- and 3-pentanol, 2-hexanol, 2- and 4-octanol, and 4-methyl- and 4,4-dimethyl-2-pentanol at 235/sup 0/-290/sup 0/C and 1 atm alcohol for 4-6 hr over zirconia catalysts prepared from various zirconium salts by precipitation and thermally pretreated in hydrogen or air gave mixtures of the corresponding ketones and alkenes. Many samples pretreated in hydrogen were very selective for dehydration of secondary (but not tertiary) 2-alkanols to alkenes, and two of them showed over 95Vertical Bar3< selectivity for 1-alkenes; the oxygen-treated catalysts were nonselective in most cases. Some of the catalysts showed high dehydrogenation selectivities for the 3- and 4-alkanols. The same nonequilibrium mixture of 3- and 1-methylcyclohexene was obtained from the conversion of pure cis- or trans-2-methylcyclohexanol over this catalyst, suggesting a common intermediate for dehydration, dehydrogenation, and cis-trans isomerization of the alcohol. Over-all, zirconia catalysts resembled thoria, but were quite different from titania and hafnia.

  17. Catalytic Oxidative Conversion from Naphthol to 2-Hydroxy-1, 4-naphthoquinone over Iron Porphyrin Catalysts by Molecular Oxygen in an Alkaline 2-Propanol Solution

    Institute of Scientific and Technical Information of China (English)

    YANG Ke-er; TONG Shan-ling; YAN Yan; KANG En-hua; XIAO Feng-shou; LI Qing; CHANG Xin; FANG Chi-guang

    2005-01-01

    In an alkaline 2-propanol solution with 5,10,15,20-tetra(4-methoxyl phenyl) porphyrin iron chloride(TOMPPFeCl) as a catalyst and oxygen as a cheap green oxidant, 2-naphthol was conversed to 2-hydroxy-1,4-naphthoquinone(HNQ) with a yield of 62.17% and a selectivity of 100%, and the conversion number of TMOPPFeCl catalyst was 8.32/min. The catalytic oxidation products were characterized by means of UV-Vis, IR, GC-MS, 1H NMR and melting point determination. In this catalytic oxidation, the catalytic activity of TMOPPFeCl was researched in detail and the reacting conditions were optimized. A possible reaction mechanism is summarized based on in situ EPR determination.

  18. Direct Catalytic Conversion of Cellulose to 5-Hydroxymethylfurfural Using Ionic Liquids

    Directory of Open Access Journals (Sweden)

    Sanan Eminov

    2016-10-01

    Full Text Available Cellulose is the single largest component of lignocellulosic biomass and is an attractive feedstock for a wide variety of renewable platform chemicals and biofuels, providing an alternative to petrochemicals and petrofuels. This potential is currently limited by the existing methods of transforming this poorly soluble polymer into useful chemical building blocks, such as 5-hydroxymethylfurfural (HMF. Ionic liquids have been used successfully to separate cellulose from the other components of lignocellulosic biomass and so the use of the same medium for the challenging transformation of cellulose into HMF would be highly attractive for the development of the biorefinery concept. In this report, ionic liquids based on 1-butyl-3-methylimidazolium cations [C4C1im]+ with Lewis basic (X = Cl− and Brønsted acidic (X = HSO4− anions were used to investigate the direct catalytic transformation of cellulose to HMF. Variables probed included the composition of the ionic liquid medium, the metal catalyst, and the reaction conditions (temperature, substrate concentration. Lowering the cellulose loading and optimising the temperature achieved a 58% HMF yield after only one hour at 150 °C using a 7 mol % loading of the CrCl3 catalyst. This compares favourably with current literature procedures requiring much longer reactions times or approaches that are difficult to scale such as microwave irradiation.

  19. Conversion of Isoprenoid Oil by Catalytic Cracking and Hydrocracking over Nanoporous Hybrid Catalysts

    Directory of Open Access Journals (Sweden)

    Toshiyuki Kimura

    2012-01-01

    Full Text Available In order to produce petroleum alternatives from biomass, a significant amount of research has been focused on oils from microalgae due to their origin, which would not affect food availability. Nanoporous hybrid catalysts composed of ns Al2O3 and zeolites have been proven to be very useful compared to traditional catalysts in hydrotreating (HT, hydrocracking (HC, and catalytic cracking (CC of large molecules. To evaluate the reaction scheme and products from model isoprenoid compounds of microalgae oil, nanoporous hybrid catalyst technologies (CC: ns Al2O3/H-USY and ns Al2O3/H-GaAlMFI; HC: [Ni-Mo/γ-Al2O3]/ns Al2O3/H-beta were studied. The major product from CC on ns Al2O3/H-USY was highly aromatic gasoline, while the product from HC was half-isoparaffinic/olefinic kerosene. Although more than 50 wt% of the products from HT/CC on the USY catalyst was liquefied petroleum gas due to overcracking, the product from HT/CC on the MFI catalyst was high-octane-number gasoline. Delightfully, the product from HT/HC was kerosene and its average number was 11, with more than 80 wt% being isoparaffinic. As a result, it was demonstrated that hydrotreating may convert isoprenoid oil from microalgae over nanoporous hybrid catalysts into a variety of products.

  20. Conversion of isoprenoid oil by catalytic cracking and hydrocracking over nanoporous hybrid catalysts.

    Science.gov (United States)

    Kimura, Toshiyuki; Liu, Chen; Li, Xiaohong; Maekawa, Takaaki; Asaoka, Sachio

    2012-01-01

    In order to produce petroleum alternatives from biomass, a significant amount of research has been focused on oils from microalgae due to their origin, which would not affect food availability. Nanoporous hybrid catalysts composed of ns Al₂O₃ and zeolites have been proven to be very useful compared to traditional catalysts in hydrotreating (HT), hydrocracking (HC), and catalytic cracking (CC) of large molecules. To evaluate the reaction scheme and products from model isoprenoid compounds of microalgae oil, nanoporous hybrid catalyst technologies (CC: ns Al₂O₃/H-USY and ns Al₂O₃/H-GaAlMFI; HC: [Ni-Mo/γ-Al₂O₃]/ns Al₂O₃/H-beta) were studied. The major product from CC on ns Al₂O₃/H-USY was highly aromatic gasoline, while the product from HC was half-isoparaffinic/olefinic kerosene. Although more than 50 wt% of the products from HT/CC on the USY catalyst was liquefied petroleum gas due to overcracking, the product from HT/CC on the MFI catalyst was high-octane-number gasoline. Delightfully, the product from HT/HC was kerosene and its average number was 11, with more than 80 wt% being isoparaffinic. As a result, it was demonstrated that hydrotreating may convert isoprenoid oil from microalgae over nanoporous hybrid catalysts into a variety of products.

  1. Demonstration of selective catalytic reduction (SCR) technology for the control of nitrogen oxide (NO sub x ) emissions from high-sulfur coal-fired boilers

    Energy Technology Data Exchange (ETDEWEB)

    1991-08-01

    The objective of this project is to demonstrate and evaluate commercially available Selective Catalytic Reduction (SCR) catalysts from US, Japanese and European catalyst suppliers on a high-sulfur US coal-fired boiler. SCR is a post-combustion nitrogen oxide (NOx) control technology that involves injecting ammonia into the flue gas generated from coal combustion in an electric utility boiler. The flue gas containing ammonia is then passed through a reactor that contains a specialized catalyst. In the presence of the catalyst, the ammonia reacts with NOx to convert it to nitrogen and water vapor, Although SCR is widely practiced in Japan and Europe, there are numerous technical uncertainties associated with applying SCR to US coals. These uncertainties include: (1) potential catalyst deactivation due to poisoning by trace metal species present in US coals that are not present in other fuel performance of the technology and effects on the balance-of-plant equipment in the presence of high amounts of SO{sub 2} and SO{sub 3}. (3) performance of a wide variety of SCR catalyst compositions, geometries and methods of manufacture under typical high-sulfur coal-fired utility operating conditions. These uncertainties will be explored by constructing a series of small-scale SCR reactors and simultaneously exposing different SCR catalysts to flue gas derived from the combustion of high sulfur US coal.

  2. Demonstration of selective catalytic reduction (SCR) technology for the control of nitrogen oxide (NO[sub x]) emissions from high-sulfur coal-fired boilers

    Energy Technology Data Exchange (ETDEWEB)

    1992-08-01

    The objective of this project is to demonstrate and evaluate commercially available Selective Catalytic Reduction (SCR) catalysts from US, Japanese and European catalyst suppliers on a high-sulfur US coal-fired boiler. SCR is a post-combustion nitrogen oxide (NO[sub x]) control technology that involves injecting ammonia into the flue gas generated from coal combustion in an electric utility boiler. The flue gas containing ammonia is then passed through a reactor that contains a specialized catalyst. In the presence of the catalyst, the ammonia reacts with NO[sub x] to convert it to nitrogen and water vapor. Although SCR is widely practiced in Japan and Europe, there are numerous technical uncertainties associated with applying SCR to US coals. These uncertainties include: (1) potential catalyst deactivation due to poisoning by trace metal species present in US coals that are not present in other fuels. (2) performance of the technology and effects on the balance-of-plant equipment in the presence of high amounts of SO[sub 2] and SO[sub 3]. (3) performance of a wide variety of SCR catalyst compositions, geometries and methods of manufacture under typical high-sulfur coal-fired utility operating conditions. These uncertainties will be explored by constructing a series of small-scale SCR reactors and simultaneously exposing different SCR catalysts to flue gas derived from the combustion of high sulfur U. S. coal.

  3. Coal liquefaction. Quarterly report, January--March 1977

    Energy Technology Data Exchange (ETDEWEB)

    None

    1977-12-01

    Current ERDA work in coal liquefaction is aimed at improved process configurations for both catalytic and non-catalytic processes to provide more attractive processing economics and lower capital investment. Coal liquefaction can now be achieved under more moderate processing conditions and more rapidly than was the case in the 1930's. The advantage of coal liquefaction is that the entire range of liquid products, including heavy boiler fuel, distillate fuel oil, gasoline, jet fuel, and diesel oil, can be produced from coal by varying the type of process and operating conditions used in the process. Furthermore, coal-derived liquid fuels also have the potential for use as chemical feedstocks. To determine the most efficient means of utilizing coal resources, ERDA is sponsoring the development of several conversion processes that are currently in the pilot plant stage. Nineteen projects under development are described and progress for each in the quarter is detailed briefly. (LTN)

  4. Solid waste management of coal conversion residuals from a commercial-size facility: environmental engineering aspects. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Bern, J.; Neufeld, R. D.; Shapiro, M. A.

    1980-11-30

    Major residuals generated by the conversion process and its auxiliary operations include: (a) coal preparation wastes; (b) gasifier ash; (c) liquefaction solids-char; (d) tail gas or flue gas desulfurization sludge; (e) boiler flyash and bottom ash; (f) raw water treatment sludge, and; (g) biosludges from process wastewater treatment. Recovered sulfur may also require disposal management. Potential environmental and health impacts from each of the residues are described on the basis of characterization of the waste in the perspective of water quality degradation. Coal gasification and liquefaction systems are described in great detail with respect to their associated residuals. Management options are listed with the conclusion that land disposal of the major residual streams is the only viable choice. On-site versus off-site disposal is analyzed with the selection of on-site operations to reduce political, social and institutional pressures, and to optimize the costs of the system. Mechanisms for prevention of leachate generation are described, and various disposal site designs are outlined. It is concluded that co-disposal feasibility of some waste streams must be established in order to make the most preferred solid waste management system feasible. Capacity requirements for the disposal operation were calculated for a 50,000 bbl/day coal liquefaction plant or 250 million SCF/day gasification operation.

  5. Catalytic Two-Stage Liquefaction (CTSL{trademark}) process bench studies and PDU scale-up with sub-bituminous coal. Final report

    Energy Technology Data Exchange (ETDEWEB)

    Comolli, A.G.; Johanson, E.S.; Karolkiewicz, W.F.; Lee, L.K.T.; Stalzer, R.H.; Smith, T.O.

    1993-03-01

    Reported are the details and results of Laboratory and Bench-Scale experiments using sub-bituminous coal conducted at Hydrocarbon Research, Inc., under DOE Contract No. DE-AC22-88PC88818 during the period October 1, 1988 to December 31, 1992. The work described is primarily concerned with testing of the baseline Catalytic Two-Stage Liquefaction (CTSL{trademark}) process with comparisons with other two stage process configurations, catalyst evaluations and unit operations such as solid separation, pretreatments, on-line hydrotreating, and an examination of new concepts. In the overall program, three coals were evaluated, bituminous Illinois No. 6, Burning Star and sub-bituminous Wyoming Black Thunder and New Mexico McKinley Mine seams. The results from a total of 16 bench-scale runs are reported and analyzed in detail. The runs (experiments) concern process variables, variable reactor volumes, catalysts (both supported, dispersed and rejuvenated), coal cleaned by agglomeration, hot slurry treatments, reactor sequence, on-line hydrotreating, dispersed catalyst with pretreatment reactors and CO{sub 2}/coal effects. The tests involving the Wyoming and New Mexico Coals are reported herein, and the tests involving the Illinois coal are described in Topical Report No. 2. On a laboratory scale, microautoclave tests evaluating coal, start-up oils, catalysts, thermal treatment, CO{sub 2} addition and sulfur compound effects were conducted and reported in Topical Report No. 3. Other microautoclave tests are described in the Bench Run sections to which they refer such as: rejuvenated catalyst, coker liquids and cleaned coals. The microautoclave tests conducted for modelling the CTSL{trademark} process are described in the CTSL{trademark} Modelling section of Topical Report No. 3 under this contract.

  6. Catalytic conversion of oxygenated compounds to low molecular weight olefins. Annual report for January 1--December 31, 1978

    Energy Technology Data Exchange (ETDEWEB)

    Anthony, R.G.

    1979-01-01

    The conversion of methanol or synthesis gas is an attractive route for producing ethylene and propylene from coal. Utilizing a chabazite ion exchanged with ammonium and rare earth chlorides, methanol is converted to ethylene, propylene, and propane with carbon yields of 70 to 90% at reaction temperatures of 360 to 450/sup 0/C and pressures from 1 to 18 atmospheres. Carbon disulfide in the feed at concentrations less than 2000 ppm increases the operating time between regenerations from four hours to twenty hours. At carbon disulfide concentrations of 3000 ppm or greater, the catalyst goes through three stages. The first is that of a dehydrogenation catalyst that produces carbon monoxide and hydrogen. The second stage produces ethylene and propylene, and finally, the third stage is a dehydration catalyst that produces dimethyl ether. Water has no detrimental effect on the catalyst, and appears to enhance its activity. Increase in pressure increases the production of propylene and propane at the expense of ethylene. X-ray diffraction studies show the formation of an ultrastable zeolite. No permanent deactivation was observed even though the catalyst was overheated once, and had been deactivated and regenerated for as many as 21 times. Ethylene yields increase as the temperature increases from 360 to 450/sup 0/C. When synthesis gas is passed over the catalyst at pressures equal to or less than 500 psi, methane and carbon dioxide are produced.

  7. Effects of low-temperature catalytic pretreatments on coal structure and reactivity in liquefaction. Final technical report, Volume 2 - hydrogenative and hydrothermal pretreatments and spectroscopic characterization using pyrolysis-GC-MS, CPMAS {sup 13}C NMR and FT-IR

    Energy Technology Data Exchange (ETDEWEB)

    Chunshan Song; Hatcher, P.G.; Saini, A.K.; Wenzel, K.A.

    1998-01-01

    It has been indicated by DOE COLIRN panel that low-temperature catalytic pretreatment is a promising approach to the development of an improved liquefaction process. This work is a fundamental study on effects of pretreatments on coal structure and reactivity in liquefaction. The main objectives of this project are to study the coal structural changes induced by low-temperature catalytic and thermal pretreatments by using spectroscopic techniques; and to clarify the pretreatment-induced changes in reactivity or convertibility of coals. As the second volume of the final report, here we summarize our work on spectroscopic characterization of four raw coals including two subbituminous coals and two bituminous coals, tetrahydrofuran (THF)-extracted but unreacted coals, the coals (THF-insoluble parts) that have been thermally pretreated. in the absence of any solvents and in the presence of either a hydrogen-donor solvent or a non-donor solvent, and the coals (THF-insoluble parts) that have been catalytically pretreated in the presence of a dispersed Mo sulfide catalyst in the absence of any solvents and in the presence of either a hydrogen-donor solvent or a non-donor solvent.

  8. Direct Production of 5-Hydroxymethylfurfural via Catalytic Conversion of Simple and Complex Sugars over Phosphated TiO2.

    Science.gov (United States)

    Atanda, Luqman; Shrotri, Abhijit; Mukundan, Swathi; Ma, Qing; Konarova, Muxina; Beltramini, Jorge

    2015-09-01

    A water-THF biphasic system containing N-methyl-2-pyrrolidone (NMP) was found to enable the efficient synthesis of 5-hydroxymethylfurfural (HMF) from a variety of sugars (simple to complex) using phosphated TiO2 as a catalyst. Fructose and glucose were selectively converted to HMF resulting in 98 % and 90 % yield, respectively, at 175 °C. Cellobiose and sucrose also gave rise to high HMF yields of 94 % and 98 %, respectively, at 180 °C. Other sugar variants such as starch (potato and rice) and cellulose were also investigated. The yields of HMF from starch (80-85 %) were high, whereas cellulose resulted in a modest yield of 33 %. Direct transformation of cellulose to HMF in significant yield (86 %) was assisted by mechanocatalytic depolymerization-ball milling of acid-impregnated cellulose. This effectively reduced cellulose crystallinity and particle size, forming soluble cello-oligomers; this is responsible for the enhanced substrate-catalytic sites contact and subsequent rate of HMF formation. During catalyst recyclability, P-TiO2 was observed to be reusable for four cycles without any loss in activity. We also investigated the conversion of the cello-oligomers to HMF in a continuous flow reactor. Good HMF yield (53 %) was achieved using a water-methyl isobutyl ketone+NMP biphasic system.

  9. Removal and Conversion of Tar in Syngas from Woody Biomass Gasification for Power Utilization Using Catalytic Hydrocracking

    Directory of Open Access Journals (Sweden)

    Jiu Huang

    2011-08-01

    Full Text Available Biomass gasification has yet to obtain industrial acceptance. The high residual tar concentrations in syngas prevent any ambitious utilization. In this paper a novel gas purification technology based on catalytic hydrocracking is introduced, whereby most of the tarry components can be converted and removed. Pilot scale experiments were carried out with an updraft gasifier. The hydrocracking catalyst was palladium (Pd. The results show the dominant role of temperature and flow rate. At a constant flow rate of 20 Nm3/h and temperatures of 500 °C, 600 °C and 700 °C the tar conversion rates reached 44.9%, 78.1% and 92.3%, respectively. These results could be increased up to 98.6% and 99.3% by using an operating temperature of 700 °C and lower flow rates of 15 Nm3/h and 10 Nm3/h. The syngas quality after the purification process at 700 °C/10 Nm3/h is acceptable for inner combustion (IC gas engine utilization.

  10. Studies on Anion Promoted Titania.1: Preparation, Characterization, and Catalytic Activity toward Alcohol and Cumene Conversion Reactions of Phosphated Titania.

    Science.gov (United States)

    Parida; Acharya; Samantaray; Mishra

    1999-09-15

    Phosphate impregnated titania samples with varying amount of phosphate have been prepared by solid-solid kneading as well as aqueous impregnation method. All the samples are characterized by XRD, TG-DTA, and N(2) adsorption-desorption isotherm. Surface area is found to increase with the increase in phosphate content up to 7.5 wt% loading and thereafter decreases. The average pore diameter and crystallite size of titania decreases with the addition of phosphate. However, total acidity (determined by base adsorption method) and the catalytic activity increases with the increase in phosphate content up to 10 wt%. Phosphated samples prepared using phosphoric acid as the source of phosphate exhibit higher acidity compared to the samples prepared using (NH(4))(3)PO(4). However, the sample prepared from (NH(4))(3)PO(4) shows the presence of both acid and basic sites. Though from the cumene conversion study it is understood that phosphated samples contain both Lewis and Brønsted acid sites, the latter predominates over the former. Copyright 1999 Academic Press.

  11. Biological CO2 conversion to acetate in subsurface coal-sand formation using a high-pressure reactor system

    Directory of Open Access Journals (Sweden)

    Yoko eOhtomo

    2013-12-01

    Full Text Available Geological CO2 sequestration in unmineable subsurface oil/gas fields and coal formations has been proposed as a means of reducing anthropogenic greenhouse gasses in the atmosphere. However, the feasibility of injecting CO2 into subsurface depends upon a variety of geological and economic conditions, and the ecological consequences are largely unpredictable. In this study, we developed a new flow-through-type reactor system to examine potential geophysical, geochemical and microbiological impacts associated with CO2 injection by simulating in situ pressure (0–100 MPa and temperature (0–70°C conditions. Using the reactor system, anaerobic artificial fluid and CO2 (flow rate: 0.002 and 0.00001 mL/min, respectively were continuously supplemented into a column comprised of bituminous coal and sand under a pore pressure of 40 MPa (confined pressure: 41 MPa at 40°C for 56 days. 16S rRNA gene analysis of the bacterial components showed distinct spatial separation of the predominant taxa in the coal and sand over the course of the experiment. Cultivation experiments using sub-sampled fluids revealed that some microbes survived, or were metabolically active, under CO2-rich conditions. However, no methanogens were activated during the experiment, even though hydrogenotrophic and methylotrophic methanogens were obtained from conventional batch-type cultivation at 20°C. During the reactor experiment, the acetate and methanol concentration in the fluids increased while the δ13Cacetate, H2 and CO2 concentrations decreased, indicating the occurrence of homo-acetogenesis. 16S rRNA genes of homo-acetogenic spore-forming bacteria related to the genus Sporomusa were consistently detected from the sandstone after the reactor experiment. Our results suggest that the injection of CO2 into a natural coal-sand formation preferentially stimulates homo-acetogenesis rather than methanogenesis, and that this process is accompanied by biogenic CO2 conversion to

  12. Coal conversion rate in 1t/d PSU liquefaction reactor; 1t/d PSU ekika hannoto ni okeru sekitan tenka sokudo no kento

    Energy Technology Data Exchange (ETDEWEB)

    Ikeda, K.; Imada, K. [Nippon Steel Corp., Tokyo (Japan); Nogami, Y.; Inokuchi, K. [Mitsui SRC Development Co. Ltd., Tokyo (Japan)

    1996-10-28

    To investigate the coal liquefaction characteristics, coal slurry samples were taken from the outlets of the reactors and slurry preheater of NEDOL process 1 t/d process supporting unit (PSU), and were analyzed. Tanito Harum coal was used for liquefaction, and the slurry was prepared with recycle solvent. Liquefaction was performed using synthetic iron sulfide catalyst at reaction temperatures, 450 and 465{degree}C. Solubility of various solid samples was examined against n-hexane, toluene, and tetrahydrofuran (THF). When considering the decrease of IMO (THF-insoluble and ash) as a characteristic of coal conversion reaction, around 20% at the outlet of the slurry preheater, around 70% within the first reactor, and several percents within the successive second and third reactors were converted against supplied coal. Increase of reaction temperature led to the increase of evaporation of oil fraction, which resulted in the decrease of actual slurry flow rate and in the increase of residence time. Thus, the conversion of coal was accelerated by the synergetic effect of temperature and time. Reaction rate constant of the coal liquefaction was around 2{times}10{sup -1} [min{sup -1}], which increased slightly with increasing the reaction temperature from 450 to 465{degree}C. 3 refs., 5 figs., 1 tab.

  13. Alternative process schemes for coal conversion. Progress report No. 4, September 1, 1979-March 30, 1980

    Energy Technology Data Exchange (ETDEWEB)

    Sansone, M.J.

    1980-04-01

    This progress report is divided into two parts. In Part A, the results of the first three progress reports which dealt with the separation of H/sub 2//CH/sub 4/ and H/sub 2//CH/sub 4//CO mixtures resulting from coal gasification processes are briefly summarized. The separation calculations were performed for ideal, cryogenic, clathrate (gas-hydrate), and absorption/stripping separation processes. The cryogenic separation indicates the least energy requirement. Work on this phase of the program has been concluded. An experimental coal gasification program is being undertaken. In Part B, a review smmary of existing and developing coal gasificaton processes is presented. The relative merits of gasifier type, heating method, operating mode, process conditions, and gasifying medium are considered. This is followed by a qualitative appraisal of several selected coal gasification processes based upon the above considerations. It is intended that this report will help focus attention on those areas in which significant process improvements can be realized. The report concludes with a series of recommendations for future work.

  14. Matrials technology for coal-conversion processes. Progress report, April-June 1980

    Energy Technology Data Exchange (ETDEWEB)

    Ellingson, W A

    1980-10-01

    The twelfth 500-h slag-refractory test run, which involved a high-iron-content acidic coal slag, was completed. High chromia content and high density were again identified as important factors in minimizing corrosion of refractories. Results from the high-temperature nondestructive erosion-scanner installation at the Solvent Refined Coal plant has revealed the presence of a hard film composed of Cr, Fe, S and O/sub 2/, which seems to reduce erosive wear but is acoustically transparent. Further improvements in the erosion-scanner data-acquisition system through employment of a correction for through-wall thermal gradients have reduced data scatter to < +- 0.05 mm. Quantitative detection of internal liquid leaks past critical valves in coal liquefaction plants seems possible through use of low-velocity ultrasonic or strain-sensitive flowmeters together with passive acoustic systems. Studies of high-temperature gaseous corrosion in low-Btu environments show that the potential exists for sulfide attack even in high-chromium alloys such as 310 SS. Recent results show that the oxygen partial pressure threshold above which a protective oxide film forms is 10/sup 3/ to 10/sup 5/ (at 1144 and 923 K, respectively) times the oxygen partial pressure for Cr oxide/Cr sulfide equilibrium. Four of the seven special thermowells installed at IGT's U-gas plant have shown no significant degradation after an additional 500-h run. Failure-analysis activities this period included analysis of a failed internal transfer line and a thermocouple sheath, both from the HYGAS coal-gasification pilot plant. A complete summary of the more important coal-gasification failures analyzed at Argonne is included in this report.

  15. Innovative clean coal technology (ICCT): Demonstration of selective catalytic reduction (SCR) technology for the control of nitrogen oxide (NO{sub x}) emissions from high-sulfur coal-fired boilers. Fourth quarterly progress report

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1992-12-31

    The objective of this project is to demonstrate and evaluate commercially available Selective Catalytic Reduction (SCR) catalysts from US, Japanese and European catalyst suppliers on a high-sulfur US coal-fired boiler. SCR is a post-combustion nitrogen oxide (NO{sub x}) control technology that involves injecting ammonia into the flue gas generated from coal combustion in an electric utility boiler. The flue gas containing ammonia is then passed through a reactor that contains a specialized catalyst. In the presence of the catalyst, the ammonia reacts with NO{sub x} to convert it to nitrogen and water vapor. Although SCR is widely practiced in Japan and Europe, there are numerous technical uncertainties include: (1) potential catalyst deactivation due to poisoning by trace metal species present in US coals that are not present in other fuels; (2) performance of the technology and effects on the balance-of-plant equipment in the presence of high amounts of SO{sub 2} and SO{sub 3}; and (3) performance of a wide variety of SCR catalyst compositions, geometries and methods of manufacture under typical high-sulfur coal-fired utility operating conditions. These uncertainties will be explored by constructing a series of small-scale SCR reactors and simultaneously exposing different SCR catalysts to flue gas derived from the combustion of high sulfur US coal.

  16. One-Pot Liquid-Phase Catalytic Conversion of Ethanol to 1-Butanol over Aluminium Oxide—The Effect of the Active Metal on the Selectivity

    Directory of Open Access Journals (Sweden)

    Jyri-Pekka Mikkola

    2012-01-01

    Full Text Available Direct catalytic valorization of bioethanol to 1-butanol over different alumina supported catalysts was studied. Thirteen (13 heterogeneous catalysts were screened in search for the optimal material composition for direct one-pot conversion of ethanol to 1-butanol. For the most promising catalyst, a 25% ethanol conversion with 80% selectivity (among liquid carbon products to 1-butanol could be reached at 250 °C. Additionally, the reaction kinetics and mechanisms were further investigated upon use of the most suitable catalyst candidate.

  17. Innovative Clean Coal Technology (ICCT): Demonstration of selective catalytic reduction technology for the control of nitrogen oxide emissions from high-sulfur coal-fired boilers. First and second quarterly technical progress reports, [January--June 1995]. Final report

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1995-12-31

    The objective of this project is to demonstrate and evaluate commercially available Selective Catalytic Reduction (SCR) catalysts from US, Japanese and European catalyst suppliers on a high-sulfur US coal-fired boiler. SCR is a post-combustion nitrogen oxide (NO{sub x}) control technology that involves injecting ammonia (NH{sub 3}) into the flue gas generated from coal combustion in an electric utility boiler. The flue gas containing ammonia is then passed through a reactor containing a specialized catalyst. In the presence of the catalyst, the ammonia reacts with NO{sub x} to convert it to nitrogen and water vapor. Although SCR is widely practiced in Japan and Europe on gas-, oil-, and low-sulfur coal-fired boilers, there are several technical uncertainties associated with applying SCR to US coals. These uncertainties include: (1) potential catalyst deactivation due to poisoning by trace metal species present in US coals that are not present in other fuels. (2) performance of the technology and effects on the balance-of-plant equipment in the presence of high amounts of SO{sub 2} and SO{sub 3}. (3) performance of a wide variety of SCR catalyst compositions, geometries, and methods of manufacture under typical high-sulfur coal-fired utility operating conditions. These uncertainties are being explored by operating a series of small-scale SCR reactors and simultaneously exposing different SCR catalysts to flue gas derived from the combustion of high sulfur US coal. The demonstration is being performed at Gulf Power Company`s Plant Crist Unit No. 5 (75 MW nameplate capacity) near Pensacola, Florida. The project is funded by the US Department of Energy (DOE), Southern Company Services, Inc. (SCS on behalf of the entire Southern electric system), the Electric Power Research Institute (EPRI), and Ontario Hydro. SCS is the participant responsible for managing all aspects of this project.

  18. Innovative Clean Coal Technology (ICCT): Demonstration of Selective Catalytic Reduction (SCR) technology for the control of nitrogen oxide (NO{sub x}) emissions from high-sulfur coal-fired boilers. Third quarterly technical progress report 1992

    Energy Technology Data Exchange (ETDEWEB)

    1992-11-01

    The objective of this project is to demonstrate and evaluate commercially available Selective Catalytic Reduction (SCR) catalysts from US, Japanese and European catalyst suppliers on a high-sulfur US coal-fired boiler. SCR is a post-combustion nitrogen oxide (NO{sub x}) control technology that involves injecting ammonia into the flue gas generated from coal combustion in an electric utility boiler. The flue gas containing ammonia is then passed through a reactor that contains a specialized catalyst. In the presence of the catalyst, the ammonia reacts with NO{sub x} to convert it to nitrogen and water vapor. Although SCR is widely practiced in Japan and Europe on gas-, oil-, and low-sulfur, coal-fired boilers, there are several technical uncertainties associated with applying SCR to US coals. These uncertainties include: (1) potential catalyst deactivation due to poisoning by trace metal species present in US coals that are not present in other fuels. (2) performance of the technology and effects on the balance-of-plant equipment in the presence of high amounts of SO{sub 2} and SO{sub 3} and (3) performance of a wide variety of SCR catalyst compositions, geometries and methods of manufacture under typical high-sulfur coal-fired utility operating conditions. These uncertainties will be explored by constructing a series of small- scale SCR reactors and simultaneously exposing different SCR catalysts to flue gas derived from the combustion of high-sulfur US coal. The demonstration will be performed at Gulf Power Company`s Plant Crist Unit No. 5 (75 MW capacity) near Pensacola, Florida.

  19. Innovative Clean Coal Technology (ICCT): Demonstration of selective catalytic reduction (SCR) technology for the control of nitrogen oxide (NO{sub x}) emissions from high-sulfur coal-fired boilers. Technical progress report, third and fourth quarters 1994

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1995-11-01

    The objective of this project is to demonstrate and evaluate commercially available selective catalytic reduction (SCR) catalysts from U.S., Japanese, and European catalyst suppliers on a high-sulfur U.S. Coal-fired boiler. SCR is a post-combustion nitrogen oxide (NO{sub x}) control technology that involves injecting ammonia into the flue gas generated from coal combustion in an electric utility boiler. The flue gas containing ammonia is then passed through a reactor that contains a specialized catalyst. In the presence of the catalyst, the ammonia reacts with NO{sub x} to form nitrogen and water vapor. Although SCR is widely practiced in Japan and European gas-, oil-, and low-sulfur coal-fired boilers, there are several technical uncertainties associated with applying SCR to U.S. coals. These uncertainties include: (1) potential catalyst deactivation due to poisoning by trace metal species present in U.S. coals that are not present in other fuels; (2) performance of the technology and effects on the balance-of-plant equipment in the presence of high amounts of SO{sub 2} and SO{sub 3}; performance of a wide variety of SCR catalyst compositions, geometries, and methods of manufacture under typical high-sulfur coal-fired utility operating conditions. These uncertainties are being explored by operating a series of small- scale SCR reactors and simultaneously exposing different SCR catalysts to flue gas derived from the combustion of high sulfur U.S. coal. The demonstration is being performed at Gulf Power Company`s Plant Crist Unit No. 5 (75 MW capacity) near Pensacola, Florida. The project is funded by the U.S. Department of Energy (DOE), Southern Company Services, Inc. (SCS on behalf of the entire Southern electric system), the Electric Power Research Institute (EPRI), and Ontario Hydro. SCS is the participant responsible for managing al aspects of this project. 1 ref., 69 figs., 45 tabs.

  20. Innovative Clean Coal Technology (ICCT): Demonstration of selective catalytic reduction (SCR) technology for the control of nitrogen oxide (NO{sub x}) emissions from high-sulfur coal-fired boilers. Technical progress report, October 1993--December 1993

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1995-06-01

    The objective of this project is to demonstrate and evaluate commercially available Selective Catalytic Reduction (SCR) catalysts from U.S., Japanese and European catalyst suppliers on a high-sulfur U.S. coal-fired boiler. SCR is a post-combustion nitrogen oxide (NO{sub x}) control technology that involves injecting ammonia into the flue gas generated from coal combustion in an electric utility boiler. The flue gas containing ammonia is then passed through a reactor that contains a specialized catalyst. In the presence of the catalyst, the ammonia reacts with NO{sub x} to convert it to nitrogen and water vapor. Although SCR is widely practiced in Japan and Europe on gas-, oil-, and low-sulfur coal-fired boilers, there are several technical uncertainties associated with applying SCR to U.S. coals. These uncertainties include: (1) potential catalyst deactivation due to poisoning by trace metal species present in U.S. coals that are not present in other fuels; (2) performance of the technology and effects on the balance-of-plant equipment in the presence of high amounts of SO{sub 2} and SO{sub 3}; and (3) performance of a wide variety of SCR catalyst compositions, geometries and methods of manufacture under typical high-sulfur coal-fired utility operating conditions. These uncertainties are being explored by operating a series of small-scale SCR reactors and simultaneously exposing different SCR catalysts to flue gas derived from the combustion of high sulfur U.S. coal.

  1. Innovative Clean Coal Technology (ICCT): Demonstration of Selective Catalytic Reduction (SCR) technology for the control of nitrogen oxide (NO[sub x]) emissions from high-sulfur coal-fired boilers

    Energy Technology Data Exchange (ETDEWEB)

    1992-11-01

    The objective of this project is to demonstrate and evaluate commercially available Selective Catalytic Reduction (SCR) catalysts from US, Japanese and European catalyst suppliers on a high-sulfur US coal-fired boiler. SCR is a post-combustion nitrogen oxide (NO[sub x]) control technology that involves injecting ammonia into the flue gas generated from coal combustion in an electric utility boiler. The flue gas containing ammonia is then passed through a reactor that contains a specialized catalyst. In the presence of the catalyst, the ammonia reacts with NO[sub x] to convert it to nitrogen and water vapor. Although SCR is widely practiced in Japan and Europe on gas-, oil-, and low-sulfur, coal-fired boilers, there are several technical uncertainties associated with applying SCR to US coals. These uncertainties include: (1) potential catalyst deactivation due to poisoning by trace metal species present in US coals that are not present in other fuels. (2) performance of the technology and effects on the balance-of-plant equipment in the presence of high amounts of SO[sub 2] and SO[sub 3] and (3) performance of a wide variety of SCR catalyst compositions, geometries and methods of manufacture under typical high-sulfur coal-fired utility operating conditions. These uncertainties will be explored by constructing a series of small- scale SCR reactors and simultaneously exposing different SCR catalysts to flue gas derived from the combustion of high-sulfur US coal. The demonstration will be performed at Gulf Power Company's Plant Crist Unit No. 5 (75 MW capacity) near Pensacola, Florida.

  2. Innovative Clean Coal Technology (ICCT). Demonstration of Selective Catalytic Reduction (SCR) technology for the control of nitrogen oxide (NO{sub x}) emissions from high-sulfur coal-fired boilers: Volume 1. Final report

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-10-01

    The objective of this project is to demonstrate and evaluate commercially available Selective Catalytic Reduction (SCR) catalysts from U.S., Japanese and European catalyst suppliers on a high-sulfur U.S. coal-fired boiler. SCR is a post-combustion nitrogen oxide (NO.) control technology that involves injecting ammonia into the flue gas generated from coal combustion in an electric utility boiler. The flue gas containing ammonia is then passed through a reactor that contains a specialized catalyst. In the presence of the catalyst, the ammonia reacts with NO. to convert it to nitrogen and water vapor. Although SCR is widely practiced in Japan and Europe on gas-, oil-, and low-sulfur coal- fired boilers, there are several technical uncertainties associated with applying SCR to U.S. coals. These uncertainties include: 1) potential catalyst deactivation due to poisoning by trace metal species present in U.S. coals that are not present in other fuels. 2) performance of the technology and effects on the balance-of- plant equipment in the presence of high amounts of SO{sub 2} and SO{sub 3}. 3) performance of a wide variety of SCR catalyst compositions, geometries and methods of manufacturer under typical high-sulfur coal-fired utility operating conditions. These uncertainties were explored by operating nine small-scale SCR reactors and simultaneously exposing different SCR catalysts to flue gas derived from the combustion of high sulfur U.S. coal. In addition, the test facility operating experience provided a basis for an economic study investigating the implementation of SCR technology.

  3. Biological CO2 conversion to acetate in subsurface coal-sand formation using a high-pressure reactor system

    Science.gov (United States)

    Ohtomo, Y.; Ijiri, A.; Ikegawa, Y.; Tsutsumi, M.; Imachi, H.; Uramoto, G.; Hoshino, T.; Morono, Y.; Tanikawa, W.; Hirose, T.; Inagaki, F.

    2013-12-01

    belonged to a methylotrophic methanogen within the genus Methanosarcina. For the acetate-fed culture, no cell proliferation and methane-production were observed after two-years incubation. During the injection of CO2 and fluid, increase of dissolved CH4 concentration was observed, of which δ13CCH4 were constantly similar to those of the absorbed coal-bed methane (δ13CCBM, ~70‰), suggesting the enhanced gas recovery with fluid flow. The output volume of CO2 (ΣCO2out, 22.1 to 125.6 mM) was smaller than initial concentration (ΣCO2in, 138.38 mM), which can be explained by either adsorption on coal, formation of carbonate minerals, or microbial consumption. Increase of acetate concentration in the fluids was also observed, whereas δ13Cacetate depleted during experiment. Considering with the decrease of additive H2, it is most likely that homo-acetogenesis would occur during experiments, which is consistent with detection of Sporomusa-related 16S rRNA genes, homo-acetogenic bacterium, in cloning analysis of sandstone after experiment. Decrease of formate concentrations and increase of δ13Cformate indicate bacterial consumption of formate and isotopic fractionation. Our results suggest that CO2 injection to natural coal-sand formation stimulates homo-acetogenesis rather than methanogenesis, accompanied by biogenic CO2 conversion to acetate.

  4. 纤维素催化转化为高附加值化学品的研究进展%Recent Developments in the Catalytic Conversion of Cellulose into Valuable Chemicals

    Institute of Scientific and Technical Information of China (English)

    Pengfei YANG; Hirokazu KOBAYASHI; Atsushi FUKUOKA

    2011-01-01

    Currently, under huge pressure from energy demands and environmental problems, much attention is bing paid to biomass conversion, which will play an important role in meeting the reauirements for a sustainable society As the most abundant biomass one, earth cellulose is usually used as the first research target for biomass conversion In this review, the recalcitrant stucture of cellulose is discussed and non-catalytic hydrolysis by hot-compressed water and catalytic hydrolysis using solid acids are then considered, we also review the catalytic conversion of cellulose into valuable chemicals including hexitols (sorbitol and mannitol), ethylene glycol, and related compourunds using various heterogeneous catalysts.

  5. Quantum chemical study on the catalytic mechanism of Na/K on NO-char heterogeneous reactions during the coal reburning process

    Institute of Scientific and Technical Information of China (English)

    Zheng-cheng WEN; Zhi-hua WANG; Jun-hu ZHOU; Ke-fa CEN

    2009-01-01

    Quantum chemical simulation was used to investigate the catalytic mechanism of Na/K on NO-char heterogeneous reactions during the coal reburning process. Both NO-char and NO-NaYK reactions were considered as three-step processes in this calculation. Based on geometry optimizations made using the UB3LYP/6-31 G(d) method, the activation energies of NO-char and NO-Na/K reactions were calculated using the QC1SD(T)/6-3 i 1G(d, p) method; Results showed that the activation energy of the NO-Na/K reaction (107.9/82.0 kJ/mol) was much lower than that of the NO-char reaction (245.1 kJ/mol). The reactions of NaO/KO and Na2P/K2O reduced by char were also studied, and their thermodynamics were calculated using the UB3LYP/6-31G(d) method; Results showed that both Na and K can be refreshed easily and rapidly by char at high temperature during the coal rebuming process. Based on the calculations and analyses, the catalytic mechanism of Na/K on NO-char het-erogeneous reactions during the coal reburning process was clarified.

  6. Oil-to-coal cavern conversion pins its success on rock bolts

    Energy Technology Data Exchange (ETDEWEB)

    Hamrin, H. (Atlas Copco MCT AB (Sweden))

    1989-07-01

    A new pressurized fluidized bed combustion power plant is being built in Stockholm. Coal will be stored underground, in old oil storage chambers. The roof had to be bolted and shotcreted and swellex bolts were used. These act as roof support with immediate action for the protection of the workers, and as a safety pin to reinforce the bond between shotcrete and the rock surface. 4 figs.

  7. Materials technology for coal-conversion processes. Progress report, January-March 1980

    Energy Technology Data Exchange (ETDEWEB)

    Ellingson, William A.

    1980-06-01

    The program entails nondestructive testing, failure analysis, and studies of erosive wear, corrosion, and refractory degradation. Analysis of recent refractory-slag interaction tests suggests that as the chromia content is increased from 10 to 32%, the primary reaction product changes from calcium hexaluminate to spinel, significantly increasing the corrosion resistance of the refractory. Field reliability of the high-temperature ultrasonic erosion scanner was demonstrated at both a coal liquefaction plant (SRC at Tacoma, WA) and a coal gasification plant (Morgantown, WV). Continuous high-temperature operation has been demonstrated and an accuracy of +-0.025 mm seems achievable. Equipment has been ordered for field tests of passive acoustic systems at Exxon. This includes a four-channel tape recorder, differential amplifiers, and signal conditioners. Corrosion studies have been completed on effects of multicomponent gas environments on corrosion mechanisms and uniaxial tensile properties of Fe-Ni-Cr alloys. Results of these and other tests utilizing 10,000-h exposures suggest that corrosion rates of 0.6 mm/y can be expected. Failure analysis activities included studies of compressor diaphragms from the Grand Forks Energy Technology Center coal-liquefaction continuous-process unit. Cracks were found in two of the three diaphragms. Failure of an internal solids transfer line from HYGAS appears to have been caused by severe localized sulfidation of the high-nickel Inconel 182 weld metal used to fabricate the line.

  8. Conversion of Aussedat Rey's Souche Mill to coal

    Energy Technology Data Exchange (ETDEWEB)

    Vallet, J.C.

    1985-04-01

    Until 1984 the Souche Mill, which belongs to the Aussedat Rey Group, was using 14,000 tons of heavy oil No.2 to produce about 50,000 tons per year of coated papers. The competitive price of coal, combined with the development of new techniques, led to the adoption of a coal-based system. The envisaged installation is a spreader stoker boiler, capable of producing 35 tons per hour of steam superheated to 460 C at 69 bars, feeding turbo-alternators. It is an all-welded water-tube boiler with diaphragm type tube bundles and a single water tank. It combines electro-static dust-removal with total soot rejection. The combustion efficiency of such a boiler plant is comparable to that of an oil-burning boiler-house (90%). The spreader stoker is suited to the burning of crushed fines from the Lorraine Basin and the majority of imported fines. The handling of the coal and ash is automated. The cost of such an installation is put at 28 million French Francs. The outlay on fuel will be 13,405 kFF instead of 25,900 kFF. The expected net profit on fuel purchases is of the order of 27% of the current price.

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

    Energy Technology Data Exchange (ETDEWEB)

    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.

  10. Impregnation of Catalytic Metals in Single-Walled Carbon Nanotubes for Toxic Gas Conversion in Life Support System

    Science.gov (United States)

    Li, Jing; Wignarajah, Kanapathipillai; Cinke, Marty; Partridge, Harry; Fisher, John

    2004-01-01

    Carbon nanotubes (CNTs) possess extraordinary properties such as high surface area, ordered chemical structure that allows functionalization, larger pore volume, and very narrow pore size distribution that have attracted considerable research attention from around the world since their discovery in 1991. The development and characterization of an original and innovative approach for the control and elimination of gaseous toxins using single walled carbon nanotubes (SWNTs) promise superior performance over conventional approaches due to the ability to direct the selective uptake of gaseous species based on their controlled pore size, increased adsorptive capacity due to their increased surface area and the effectiveness of carbon nanotubes as catalyst supports for gaseous conversion. We present our recent investigation of using SWNTs as catalytic supporting materials to impregnate metals, such as rhodium (Rh), palladium (Pd) and other catalysts. A protocol has been developed to oxidize the SWNTs first and then impregnate the Rh in aqueous rhodium chloride solution, according to unique surface properties of SWNTs. The Rh has been successfully impregnated in SWNTs. The Rh-SWNTs have been characterized by various techniques, such as TGA, XPS, TEM, and FTIR. The project is funded by a NASA Research Announcement Grant to find applications of single walled nanocarbons in eliminating toxic gas Contaminant in life support system. This knowledge will be utilized in the development of a prototype SWNT KO, gas purification system that would represent a significant step in the development of high efficiency systems capable of selectively removing specific gaseous for use in regenerative life support system for human exploration missions.

  11. Reaction kinetics study of coal catalytic gasification in lab scale fixed bed reactor%小型固定床煤催化气化动力学研究

    Institute of Scientific and Technical Information of China (English)

    高攀; 顾松园; 钟思青; 金永明; 曹勇

    2015-01-01

    K2CO3 catalytic gasification of Neimeng brown coal was studied in a fixed bed reactor. The effects of catalyst loading, temperature, gasification agents, such as H2O and H2, and partial pressure of H2O on the carbon conversion and reaction rate were investigated. The results showed that K2CO3 could accelerated the rate of coal-steam gasification obviously, and the carbon conversion reached 70% with the addition of only 10% K2CO3 by mass at 700℃, while H2 inhibited the coal-steam gasification seriously. A kinetic reaction equation was proposed based on an n order and Langmuir-Hinshewood expression by evaluating the carbon conversion behavior. The gasification activity significantly increased with steam partial pressure. In the n order expression, the order nwas 0.87 and the activation energy was 169.2kJ/mol, and, in the L-H expression, the activation energy was 121.9kJ/mol.%以K2CO3和内蒙褐煤为研究对象,在小型固定床上考察了催化剂负载量、温度,氢气以及水蒸气分压对碳转化率和气化反应速率的影响。结果表明,K2CO3对煤焦-水蒸气气化反应有明显的催化作用,700℃,当添加10%的K2CO3,碳的转化率为70%,氢气的含量对煤焦-水蒸气的反应有明显的抑制作用,并采用n级速率方程和Langmuir-Hinshelwood速率方程考察了水蒸气分压的影响,分压提高,煤焦-水蒸气气化反应活性提高,采用n级速率方程得到煤-水蒸气气化反应级数为0.87,活化能为169.2kJ/mol;采用L-H方程得到活化能为121.9kJ/mol。

  12. Catalytic Conversion of Biofuels

    DEFF Research Database (Denmark)

    Jørgensen, Betina

    oxidation of ethanol to form acetyl compounds. The steam reforming has been covered by a literature study of the research work done so far giving an introduction to the use of ethanol as a feedstock. The partial oxidation of ethanol has been studied experimentally using gold and vanadium based heterogeneous...... catalysts, and two different experimental methods, namely, a batch system and a continuous flow system. In the batch reaction the process was carried out in the liquid phase using a gold catalyst and atmospheric air as the oxidant. Experiments were conducted at moderate pressures and temperatures (90-200 °C...

  13. Catalytic Fuel Conversion Facility

    Data.gov (United States)

    Federal Laboratory Consortium — This facility enables unique catalysis research related to power and energy applications using military jet fuels and alternative fuels. It is equipped with research...

  14. Cooperative research program in coal liquefaction

    Energy Technology Data Exchange (ETDEWEB)

    Huffman, G.P. (ed.)

    1991-01-01

    This Quarterly Report on coal liquefaction research includes discussion in the areas of (1) Iron Based Catalysts for Coal Liquefaction; (2) Exploratory Research on Coal Conversion; (3) Novel Coal Liquefaction Concepts; (4) Novel Catalysts for Coal Liquefaction. (VC)

  15. Demonstration of Selective Catalytic Reduction (SCR) technology for the control of nitrogen oxide (NO sub x ) emissions from high-sulfur coal-fired boilers: Innovative Clean Coal Technology (ICCT)

    Energy Technology Data Exchange (ETDEWEB)

    1992-05-01

    The objective of this project is to demonstrate and evaluate commercially available Selective Catalytic Reduction (SCR) catalysts from US, Japanese and European catalyst suppliers on a high-sulfur US coal-fired boiler. SCR is a post-combustion nitrogen oxide (NO{sub x}) control technology that involves injecting ammonia into the flue gas generated from coal combustion in an electric utility boiler. The flue gas containing ammonia is then passed through a reactor that contains a specialized catalyst. In the presence of the catalyst, the amonia reacts with NO{sub x} to convert it to nitrogen and water vapor. Although SCR is widely practiced in Japan and Europe, there are numerous technical uncertainties associated with applying SCR to US coals. These uncertainties include: (1) potential catalyst deactivation due to poisoning by trace metal species present in US coals that are not present in other fuels. (2) performance of the technology and effects on the balance-of-plant equipment in the presence of high amounts of SO, and SO{sub 3}. (3) performance of a wide variety of SCR catalyst compositions, geometries and methods of manufacture under typical high-sulfur coal-fired utility operating conditions. These uncertainties will be explored by constructing a series of small-scale SCR reactors and simultaneously exposing different SCR catalysts to flue gas derived from the combustion of high sulfur US coal. The demonstration will be performed at Gulf Power Company's Plant Crist Unit No. 5 (75 MW capacity) near Pensacola, Florida. The project will be funded by the US Department of Energy (DOE), Southern Company Services, Inc. (SCS on behalf of the entire Southern electric system), and the Electric Power Research Institute.

  16. Demonstration of Selective Catalytic Reduction (SCR) technology for the control of nitrogen oxide (NO{sub x}) emissions from high-sulfur coal-fired boilers: Innovative Clean Coal Technology (ICCT). Quarterly report No. 7, January--March 1992

    Energy Technology Data Exchange (ETDEWEB)

    1992-05-01

    The objective of this project is to demonstrate and evaluate commercially available Selective Catalytic Reduction (SCR) catalysts from US, Japanese and European catalyst suppliers on a high-sulfur US coal-fired boiler. SCR is a post-combustion nitrogen oxide (NO{sub x}) control technology that involves injecting ammonia into the flue gas generated from coal combustion in an electric utility boiler. The flue gas containing ammonia is then passed through a reactor that contains a specialized catalyst. In the presence of the catalyst, the amonia reacts with NO{sub x} to convert it to nitrogen and water vapor. Although SCR is widely practiced in Japan and Europe, there are numerous technical uncertainties associated with applying SCR to US coals. These uncertainties include: (1) potential catalyst deactivation due to poisoning by trace metal species present in US coals that are not present in other fuels. (2) performance of the technology and effects on the balance-of-plant equipment in the presence of high amounts of SO, and SO{sub 3}. (3) performance of a wide variety of SCR catalyst compositions, geometries and methods of manufacture under typical high-sulfur coal-fired utility operating conditions. These uncertainties will be explored by constructing a series of small-scale SCR reactors and simultaneously exposing different SCR catalysts to flue gas derived from the combustion of high sulfur US coal. The demonstration will be performed at Gulf Power Company`s Plant Crist Unit No. 5 (75 MW capacity) near Pensacola, Florida. The project will be funded by the US Department of Energy (DOE), Southern Company Services, Inc. (SCS on behalf of the entire Southern electric system), and the Electric Power Research Institute.

  17. The formation mechanism of CO{sub 2} and its conversion in the process of coal gasification under arc plasma conditions

    Energy Technology Data Exchange (ETDEWEB)

    He, X.J.; Zheng, M.D.; Qiu, J.S.; Zhao, Z.B.; Ma, T.C. [Dalian University of Technology, Dalian (China). Carbon Research Laboratory

    2006-05-15

    The carbon dioxide (CO{sub 2}) formation mechanism and co-conversion of CO{sub 2} with coal was investigated in the process of coal gasification in a steam medium at atmospheric pressure under arc plasma conditions in a tube-type setup. The arc plasma was diagnosed in situ by optical emission spectroscopy and the gas products were analysed by gas chromatography. CO{sub 2} yields are correlated with the quantitative emission peak intensity of the active species in plasma when the operating parameter is changed. The results show that the greater the emission peak intensity of the CH radicals, C2 radicals, OH radicals or O atoms, the smaller the CO{sub 2} yield is, which means that the CO{sub 2} formation process is inhibited by increasing the concentration of the mentioned active species under arc plasma conditions. On the basis of the diagnosis results, co-conversion of CO{sub 2} and coal in a steam medium under plasma conditions was carried out in the same setup and the results show that CO{sub 2} conversion reaches 88.6% while the concentration of CO + H{sub 2} reaches 87.4%; at the same time, coal conversion is in the range 54.7 - 68.7%, which proves that co-conversion of CO{sub 2} and coal in a steam medium under plasma conditions might be a prospective way to utilize CO{sub 2} and the production of synthesis gas.

  18. The formation mechanism of CO{sub 2} and its conversion in the process of coal gasification under arc plasma conditions

    Energy Technology Data Exchange (ETDEWEB)

    He Xiaojun [School of Chemistry and Chemical Engineering, Anhui University of Technology, 59 Hudong Road, Maanshan 243002 (China); Zheng Mingdong [School of Chemistry and Chemical Engineering, Anhui University of Technology, 59 Hudong Road, Maanshan 243002 (China); Qiu Jieshan [Carbon Research Laboratory, School of Chemical Engineering, State Key Lab of Fine Chemical, Dalian University of Technology, 158 Zhongshan Road, Dalian 116012 (China); Zhao Zongbin [Carbon Research Laboratory, School of Chemical Engineering, State Key Lab of Fine Chemical, Dalian University of Technology, 158 Zhongshan Road, Dalian 116012 (China); Ma Tengcai [State Key Lab for Material Modification by Laser, Ion and Electron Beams, Dalian University of Technology, Dalian 116023 (China)

    2006-05-15

    The carbon dioxide (CO{sub 2}) formation mechanism and co-conversion of CO{sub 2} with coal was investigated in the process of coal gasification in a steam medium at atmospheric pressure under arc plasma conditions in a tube-type setup. The arc plasma was diagnosed in situ by optical emission spectroscopy and the gas products were analysed by gas chromatography. CO{sub 2} yields are correlated with the quantitative emission peak intensity of the active species in plasma when the operating parameter is changed. The results show that the greater the emission peak intensity of the CH radicals, C{sub 2} radicals, OH radicals or O atoms, the smaller the CO{sub 2} yield is, which means that the CO{sub 2} formation process is inhibited by increasing the concentration of the mentioned active species under arc plasma conditions. On the basis of the diagnosis results, co-conversion of CO{sub 2} and coal in a steam medium under plasma conditions was carried out in the same setup and the results show that CO{sub 2} conversion reaches 88.6% while the concentration of CO + H{sub 2} reaches 87.4%; at the same time, coal conversion is in the range 54.7-68.7%, which proves that co-conversion of CO{sub 2} and coal in a steam medium under plasma conditions might be a prospective way to utilize CO{sub 2} and the production of synthesis gas.

  19. Preconversion processing of bituminous coals: New directions to improved direct catalytic coal liquefaction. Quarterly report, January 1, 1992--March 31, 1992

    Energy Technology Data Exchange (ETDEWEB)

    1992-07-01

    A study of the high-temperature soaking started in this quarter, following the installation of reactors in the previous quarter. Two high-volatile bituminous coals and three coal liquids, which were identified in the previous report, were used. A cross-linked, three-dimensional macromolecular model has been widely accepted f or the structure of coal, but there is no direct evidence to prove this model. The conventional coal structure model has been recently re-examined by this investigator because of the importance of relatively strong intra- and intermolecular interactions in bituminous coals. It was reasonable to deduce that significant portions were physically associated after a study of multistep extractions, associative equilibria, the irreversibility and the dependence of coal concentration on solvent swelling, and consideration of the monophase concept. Physical dissociation which may be significant above 300{degree}C should be utilized for the treatment before liquefaction. The high-temperature soaking in a recycle oil was proposed to dissociate coal complexes.

  20. Three-phase catalytic system of H2O, ionic liquid, and VOPO4-SiO2 solid acid for conversion of fructose to 5-hydroxymethylfurfural.

    Science.gov (United States)

    Tian, Chengcheng; Zhu, Xiang; Chai, Song-Hai; Wu, Zili; Binder, Andrew; Brown, Suree; Li, Lin; Luo, Huimin; Guo, Yanglong; Dai, Sheng

    2014-06-01

    Efficient transformation of biomass-derived feedstocks to chemicals and fuels remains a daunting challenge in utilizing biomass as alternatives to fossil resources. A three-phase catalytic system, consisting of an aqueous phase, a hydrophobic ionic-liquid phase, and a solid-acid catalyst phase of nanostructured vanadium phosphate and mesostructured cellular foam (VPO-MCF), is developed for efficient conversion of biomass-derived fructose to 5-hydroxymethylfurfural (HMF). HMF is a promising, versatile building block for production of value-added chemicals and transportation fuels. The essence of this three-phase system lies in enabling the isolation of the solid-acid catalyst from the aqueous phase and regulation of its local environment by using a hydrophobic ionic liquid, 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([BMIM][Tf2N]). This system significantly inhibits the side reactions of HMF with H2O and leads to 91 mol % selectivity to HMF at 89 % of fructose conversion. The unique three-phase catalytic system opens up an alternative avenue for making solid-acid catalyst systems with controlled and locally regulated microenvironment near catalytically active sites by using a hydrophobic ionic liquid.

  1. Preliminary draft industrial siting administration permit application: Socioeconomic factors technical report. Final technical report, November 1980-May 1982. [Proposed WyCoalGas project in Converse County, Wyoming

    Energy Technology Data Exchange (ETDEWEB)

    1982-01-01

    Under the with-project scenario, WyCoalGas is projected to make a difference in the long-range future of Converse County. Because of the size of the proposed construction and operations work forces, the projected changes in employment, income, labor force, and population will alter Converse County's economic role in the region. Specifically, as growth occurs, Converse County will begin to satisfy a larger portion of its own higher-ordered demands, those that are currently being satisfied by the economy of Casper. Business-serving and household-serving activities, currently absent, will find the larger income and population base forecast to occur with the WyCoalGas project desirable. Converse County's economy will begin to mature, moving away from strict dependence on extractive industries to a more sophisticated structure that could eventually appeal to national, and certainly, regional markets. The technical demand of the WyCoalGas plant will mean a significant influx of varying occupations and skills. The creation of basic manufacturing, advanced trade and service sectors, and concomitant finance and transportation firms will make Converse County more economically autonomous. The county will also begin to serve market center functions for the smaller counties of eastern Wyoming that currently rely on Casper, Cheyenne or other distant market centers. The projected conditions expected to exist in the absence of the WyCoalGas project, the socioeconomic conditions that would accompany the project, and the differences between the two scenarios are considered. The analysis is keyed to the linkages between Converse County and Natrona County.

  2. Uncertainty estimation by Bayesian approach in thermochemical conversion of walnut hull and lignite coal blends.

    Science.gov (United States)

    Buyukada, Musa

    2017-05-01

    The main purpose of the present study was to incorporate the uncertainties in the thermal behavior of walnut hull (WH), lignite coal, and their various blends using Bayesian approach. First of all, thermal behavior of related materials were investigated under different temperatures, blend ratios, and heating rates. Results of ultimate and proximate analyses showed the main steps of oxidation mechanism of (co-)combustion process. Thermal degradation started with the (hemi-)cellulosic compounds and finished with lignin. Finally, a partial sensitivity analysis based on Bayesian approach (Markov Chain Monte Carlo simulations) were applied to data driven regression model (the best fit). The main purpose of uncertainty analysis was to point out the importance of operating conditions (explanatory variables). The other important aspect of the present work was the first performance evaluation study on various uncertainty estimation techniques in (co-)combustion literature.

  3. China Pushes Ahead with Technology for "Conversion of Coal into Oil"

    Institute of Scientific and Technical Information of China (English)

    2001-01-01

    @@ Chinese's Academy of Sciences has recently announced an R&D project of a pilot plant scale process on the basis of the Fischer-Tropsch synthesis technology developed in the Institute of Coal Chemistry (ICC),according to the recent reports from the Chinese news media.Currently, major breakthroughs have been made in the low cost catalyst production, the efficient reactor design, and the process integration, Sun Yuhan, director of ICC, said recently. He added that recent technology developed in ICC has greatly reduced the cost ofsynthesis part in the whole process, indicating the economic and environmental feasibility for the development of commercial complexes in China, and a pilot plant test is under way in coalenriched Shanxi province.

  4. Conversations among coal miners in a campaign to promote hearing protection

    Energy Technology Data Exchange (ETDEWEB)

    Stephenson, M.T.; Quick, B.L.; Witte, K.; Vaught, C.; Booth-Butterfield, S.; Patel, D. [University of Illinois, Urbana, IL (United States)

    2009-07-01

    Although working in a coal mine can diminish one's hearing capabilities by 50%, not until 2000 did federal laws require companies to establish noise standards in order to help prevent hearing loss among their employees. Since then, researchers have worked with safety administrators to develop effective messages promoting hearing protection and testing. This research assessed the effects of campaign messages on discussing campaign postcards and talking with others about a helmet-sticker incentive. The results, which are discussed with a focus on future campaigns, indicate that hearing-related attitudes, intentions, and behaviors are the most influenced by messages that were affectively neutral and least influenced by messages that were affectively negative.

  5. Materials technology for coal-conversion processes. Sixteenth quarterly report, October--December 1978

    Energy Technology Data Exchange (ETDEWEB)

    Ellingson, W A

    1978-01-01

    Refractories for slag containment, nondestructive evaluation methods, corrosion, erosion, and component failures were studied. Analysis of coal slags reveal ferritic contents of 18 to 61%, suggesting a partial pressure of 0/sub 2/ in the slagging zone of approx. 10/sup -2/ to 10/sup -4/ Pa. A second field test of the high-temperature ultrasonic erosion-monitoring system was completed. Ultrasonic inspecton of the HYGAS cyclone separator shows a reduced erosive-wear rate at 5000 h in the stellite region. The acoustic leak-detection system for valves was field tested using a 150-mm-dia. valve with a range of pressures from 0.34 to 4.05 MPa. Results suggest a linear relation between detected rms levels and leak rates. Studies on acoustic emissions from refractory concrete continued with further development of a real-time data acquisition system. Corrosion studies were conducted on Incoloy 800, Type 310 stainless steel, Inconel 671 and U.S. Steel Alloy 18-18-2 (as-received, thermally aged, and preexposed for 3.6 Ms to multicomponent gas mixtures). Results suggest a decrease in ultimate tensile strength and flow stress after preexposure. Examination of commercial iron- and nickel-base alloys after 100-h exposures in atmospheric-pressure fluidized-bed combustors suggests that the addition of 0.3 mole % CaCl/sub 2/ to the fluidized bed has no effect on the corrosion behavior of these materials; however, 0.5 mole % NaCl increased the corrosion rate of all materials. Failure-analysis activities included (1) the design and assembly of thermowells (Haynes Alloy 188 and slurry-coated Type 310 stainless steel) and (2) examination of components from the Synthane boiler explosion, the IGT Steam--Iron Pilot Plant, the HYGAS Ash Agglomerating Gasifier, and the Westinghouse Coal Gasification PDU.

  6. Cellulosic Biomass Sugars to Advantaged Jet Fuel – Catalytic Conversion of Corn Stover to Energy Dense, Low Freeze Point Paraffins and Naphthenes

    Energy Technology Data Exchange (ETDEWEB)

    Cortright, Randy [Virent, Inc., Madison, WI (United States)

    2015-07-31

    The purpose of this project was to demonstrate the technical and commercial feasibility of producing liquid fuels, particularly jet fuel, from lignocellulosic materials, such as corn stover. This project was led by Virent, Inc. (Virent) which has developed a novel chemical catalytic process (the BioForming® platform) capable of producing “direct replacement” liquid fuels from biomass-derived feedstocks. Virent has shown it is possible to produce an advantaged jet fuel from biomass that meets or exceeds specifications for commercial and military jet fuel through Fuel Readiness Level (FRL) 5, Process Validation. This project leveraged The National Renewable Energy Lab’s (NREL) expertise in converting corn stover to sugars via dilute acid pretreatment and enzymatic hydrolysis. NREL had previously developed this deconstruction technology for the conversion of corn stover to ethanol. In this project, Virent and NREL worked together to condition the NREL generated hydrolysate for use in Virent’s catalytic process through solids removal, contaminant reduction, and concentration steps. The Idaho National Laboratory (INL) was contracted in this project for the procurement, formatting, storage and analysis of corn stover and Northwestern University developed fundamental knowledge of lignin deconstruction that can help improve overall carbon recovery of the combined technologies. Virent conducted fundamental catalytic studies to improve the performance of the catalytic process and NREL provided catalyst characterization support. A technoeconomic analysis (TEA) was conducted at each stage of the project, with results from these analyses used to inform the direction of the project.

  7. Coal liquefaction. Quarterly report, July--September 1977

    Energy Technology Data Exchange (ETDEWEB)

    None

    1978-02-01

    ERDA's program for the conversion of coal to liquid fuels is aimed at improved process configurations for both catalytic and noncatalytic processes to provide more attractive processing economics and lower capital investment. The advantage of coal liquefaction is that the entire range of liquid products, including heavy boiler fuel, distillate fuel oil, gasoline, jet fuel, and diesel oil, can be produced from coal by varying the type of process and operating conditions used in the process. Furthermore, coal-derived liquids also have the potential for use as chemical feedstocks. To provide efficient and practical means of utilizing coal resources, ERDA is sponsoring the development of several conversion processes that are currently in the pilot plant stage. Responsibility for the design, construction, and operation of these facilities is given and progress in the quarter is summarized. Several supporting or complementary projects are described similarly. (LTN)

  8. Coal liquefaction. Quarterly report, April--June 1977

    Energy Technology Data Exchange (ETDEWEB)

    None

    1978-01-01

    The United States has more energy available in coal than in petroleum, natural gas, oil shale, and tar sands combined. Nationwide energy shortages, together with the availability of abundant coal reserves, make commercial production of synthetic fuels from coal vital to the Nation's total supply of clean energy. In response to this need, the Office of Fossil Energy of the Energy Research and Development Administration (ERDA) is conducting a research and development program to provide technology that will permit rapid commercialization of processes for converting coal to synthetic liquid and gaseous fuels and for improved direct combustion of coal. These fuels must be storable and suitable for power generation, transportation, and residential and industrial uses. ERDA's program for the conversion of coal to liquid fuels was begun by two of ERDA's predecessor agencies: Office of Coal Research (OCR) in 1962, and Bureau of Mines, U.S. Department of the Interior, in the 1930's. Current work in coal liquefaction is aimed at improved process configurations for both catalytic and non-catalytic processes to provide more attractive processing economics and lower capital investment. Coal liquefaction can now be achieved under more moderate processing conditions and more rapidly than was the case in the 1930's. The advantage of coal liquefaction is that the entire range of liquid products, including heavy boiler fuel, distillate fuel oil, gasoline, jet fuel, and diesel oil, can be produced from coal by varying the type of process and operating conditions used in the process. Furthermore, coal-derived liquid fuels also have the potential for use as chemical feedstocks. To determine the most efficient means of utilizing coal resources, ERDA is sponsoring the development of several conversion processes that are currently in the pilot plant stage. Nineteen projects under development are described and progress for each in the quarter is detailed briefly

  9. Application of the SULF-X process to coal conversion and utilization. Phase II final report

    Energy Technology Data Exchange (ETDEWEB)

    Shapiro, E.; Bramer, H.C.; New, R.A.

    1984-01-01

    Pittsburgh Environmental and Energy Systems, Inc. contracted with the Department of Energy to demonstrate the efficacy of an iron sulfide flue gas treatment system (FGT) for removing sulfur dioxide (SO/sub 2/) and nitrogen oxides (NO/sub x/) and to correlate process variables to system performance. Laboratory and bench-scale testing was conducted with the SULF-X process, using both synthesized gas and actual flue gas from a coal-fired furnace. Laboratory tests resulted in 95% SO/sub 2/ removal and up to 95% NO/sub x/ removal. The bench-scale system demonstrated similar SO/sub 2/ removal efficiencies, but achieved only 39% NO/sub x/ removal due to relatively high oxygen concentrations in the flue gas and insufficient liquid-gas interfacial area within the absorber. Elemental sulfur was recovered during the regeneration steps. Total capital investment for the SULF-X system was estimated to be $91 to $103 per kilowatt (electric), compared to $90/kw for sodium solution scrubbing, $78 to $83/kw for magnesia slurry scrubbing and $74/kw for limestone slurry scrubbing. Annual operating costs for the SULF-X system were estimated to be 5.44 to 6.90 mills per kilowatt-hour, compared to 4.96 to 5.22 for sodium, 3.68 to 3.99 for magnesia and 3.73 to 4.25 for limestone. 6 references, 6 figures, 9 tables.

  10. H3PO4/Al2O3 catalysts: characterization and catalytic evaluation of oleic acid conversion to biofuels and biolubricant

    OpenAIRE

    Lucia Regina Raddi de Araujo; Cynthia Fraga Scofield; Nídia Maria Ribeiro Pastura; Wilma de Araujo Gonzalez

    2006-01-01

    Al2O3 and H3PO4/Al2O3 catalysts were investigated in the conversion of oleic acid to biofuels and biolubricant at 1 atm and at 623 K. The catalytic tests were performed in a fixed bed and continuous flow reactor, using an oleic acid-catalyst ratio of 4 and N2 as the carrier gas. The reaction products were analyzed by gas chromatography and acidity measurements. N2 adsorption-desorption, X ray diffraction, 31P nuclear magnetic resonance and FT-IR spectroscopy were also employed to evaluate the...

  11. Coal conversion processes and analysis methodologies for synthetic fuels production. [technology assessment and economic analysis of reactor design for coal gasification

    Science.gov (United States)

    1979-01-01

    Information to identify viable coal gasification and utilization technologies is presented. Analysis capabilities required to support design and implementation of coal based synthetic fuels complexes are identified. The potential market in the Southeast United States for coal based synthetic fuels is investigated. A requirements analysis to identify the types of modeling and analysis capabilities required to conduct and monitor coal gasification project designs is discussed. Models and methodologies to satisfy these requirements are identified and evaluated, and recommendations are developed. Requirements for development of technology and data needed to improve gasification feasibility and economies are examined.

  12. Systems studies of coal-conversion processes using a reference simulator. Final report, March 12, 1976-August 12, 1979

    Energy Technology Data Exchange (ETDEWEB)

    Reklaitis, G.V.; Sood, M.K.; Soni, Y.; Overturf, B.W.; Wiede, W.; Clark, S.; Buchanan, P.

    1979-12-01

    Methodology and general purpose software were developed which do allow computer-aided design and analysis of large scale coal conversion processes. The LINBAL package for larger scale balance calculations was demonstrated to be quick and efficient in solving problems involving over 100 streams, 20 species, and 80 or more flowsheet units. The LSP simulation package embodies constraint handling, recycle calculation, and information management features which are an advance of the state of the art. The two level strategy available in LSP was demonstrated on a reasonable sized simulation and shown to result in a 1/3 reduction of CPU time over conventional calculation strategies. The Physical Properties Package was used in all of the simulation models developed under this project and proved to be satisfactory within the limits of the thermodynamic correlations and estimation methods which are encoded. Although the package is largely conventional in overall design, it does employ features which make it convenient to use both within LSP and on a stand-along basis. The PCOST package represents a new approach to the design of this type of program. The program has proved to be simple to use, robust, and accurate within the limitations of the literature cost correlations that it contains. In summary, the project has accomplished its primary objectives. However, time and fiscal limitation did not permit the completion of an adequate slate of case studies.

  13. Processing needs and methodology for wastewaters from the conversion of coal, oil shale, and biomass to synfuels

    Energy Technology Data Exchange (ETDEWEB)

    1980-05-01

    The workshop identifies needs to be met by processing technology for wastewaters, and evaluates the suitability, approximate costs, and problems associated with current technology. Participation was confined to DOE Environmental Control Technology contractors to pull together and integrate past wastewater-related activities, to assess the status of synfuel wastewater treatability and process options, and to abet technology transfer. Particular attention was paid to probable or possible environmental restrictions which cannot be economically met by present technology. Primary emphasis was focussed upon process-condensate waters from coal-conversion and shale-retorting processes. Due to limited data base and time, the workshop did not deal with transients, upsets, trade-offs and system optimization, or with solids disposal. The report is divided into sections that, respectively, survey the water usage and effluent situation (II); identify the probable and possible water-treatment goals anticipated at the time when large-scale plants will be constructed (III); assess the capabilities, costs and shortcomings of present technology (IV); explore particularly severe environmental-control problems (V); give overall conclusions from the Workshop and recommendations for future research and study (VI); and, finally, present Status Reports of current work from participants in the Workshop (VII).

  14. Biological mineral range effects on biomass conversion to aromatic hydrocarbons via catalytic fast pyrolysis over HZSM-5

    Science.gov (United States)

    A set of 20 biomass samples, comprising 10 genotypes of switchgrass, sorghum and miscanthus grown in two different soils with high and low poultry manure input conditions, and having a wide biological range of mineral content, were subjected to catalytic fast pyrolysis (CFP) over HZMS-5 using py-G...

  15. Catalytic conversion of methane to methanol on Cu-SSZ-13 using N2O as oxidant.

    Science.gov (United States)

    Ipek, B; Lobo, R F

    2016-11-08

    Direct catalytic methanol production from methane is achieved on Cu-SSZ-13 zeolite catalysts using N2O as the oxidant. The methanol production rate on Cu-SSZ-13 (on a per gram basis) was more than twice the rate on Cu-mordenite and more than four times the rate on Cu-ZSM-5.

  16. A catalytic biofuel production strategy involving separate conversion of hemicellulose and cellulose using 2-sec-butylphenol (SBP) and lignin-derived (LD) alkylphenol solvents.

    Science.gov (United States)

    Kim, Sunghoon; Han, Jeehoon

    2016-03-01

    A strategy in which the hemicellulose and cellulose fractions of lignocellulosic biomass are converted separately to jet fuel-range liquid hydrocarbon fuels (butene oligomers) through catalytic processes is developed. Dilute sulfuric acid (SA)-catalyzed pretreatment fractionates the first biomass into cellulose and hemicellulose-derived xylose, and these are then converted separately to levulinic acid (LA) using 2-sec-butylphenol (SBP) and lignin-derived (LD) alkylphenol solvents, respectively. LA is upgraded catalytically to butene oligomers via γ-valerolactone (GVL) and butene intermediates. Separation subsystems are designed to recover the alkylphenol solvents and biomass-derived intermediates (LA and GVL) for combination with the catalytic conversion subsystems of hemicellulose, cellulose, and lignin. In addition, a heat exchanger network (HEN) design is presented to satisfy the energy requirements of the integrated process from combustion of biomass residues (degradation products). Finally, a technoeconomic analysis shows that the proposed process ($3.37/gallon of gasoline) is an economically competitive alternative to current biofuel production approaches.

  17. Product distribution from yallourn coal by methane microwave plasma conversion; Metankaikuroha purazuma niyoru yarunsumi no tenkan hanno. Gentansochugenso no seiseibutsu heno bunpai

    Energy Technology Data Exchange (ETDEWEB)

    Kamei, Osamu; Matushima, Wataru; Kobayashi, Motoki; Onoe, Kaoru; Yamaguchi, Tatsuaki [Chiba Institute of Technologu, Chiba (Japan); Kawai, Satoshi; Ito, Yoichi

    1999-09-01

    A direct conversion technology of brown coal into relatively important fuels, raw-material gases, and residues of upgraded carbon content by use of methane microwave plasma was developed. Changes with time in the C, H, O contents of each product from Yallourn coal ware examined. The desiccated coal was packed in the middle of a cylindrical quartz tube reactor of 25.0 mm inside diameter and 400 mm length. 2.45 GHz of microwaves with desired power level controlled by a waveguide tuner was irradiated onto the upperside of the packed bed by supplying methane (4.0 kPa) successively, and the following results were obtained: (1) Both the C and H supplied from methane were converted into gaseous products (mainly of acetylene and hydrogen). (2) Within 2 minutes of reaction, C contained in the coal was converted to oily products composing mainly of aliphatic hydrocarbons in the H/C ratio range from 1.5 to 1.6; however, after 5 minutes of reaction, it was converted to carbon dioxide. (3) Almost all of the O in coal was converted to and distributed as gaseous products (finally as carbon monoxide) via disintegration of the carboxyl groups and homogeneous transformation of the carbon dioxide produced. (author)

  18. RESIDUES FROM COAL CONVERSION AND UTILIZATION: ADVANCED MINERALOGICAL CHARACTERIZATION AND DISPOSED BYPRODUCT DIAGENESIS

    Energy Technology Data Exchange (ETDEWEB)

    Gregory J. McCarthy; Dean G. Grier

    2001-01-01

    Prior to the initiation of this study, understanding of the long-term behavior of environmentally-exposed Coal Combustion By-Products (CCBs) was lacking in (among others) two primary areas addressed in this work. First, no method had been successfully applied to achieve full quantitative analysis of the partitioning of chemical constituents into reactive or passive crystalline or noncrystalline compounds. Rather, only semi-quantitative methods were available, with large associated errors. Second, our understanding of the long-term behavior of various CCBs in contact with the natural environment was based on a relatively limited set of study materials. This study addressed these areas with two objectives, producing (1) a set of protocols for fully quantitative phase analysis using the Rietveld Quantitative X-ray Diffraction (RQXRD) method and (2) greater understanding of the hydrologic and geochemical nature of the long-term behavior of disposed and utilized CCBs. The RQXRD technique was initially tested using (1) mixtures of National Institute of Standards and Technology (NIST) crystalline standards, and (2) mixtures of synthetic reagents simulating various CCBs, to determine accuracy and precision of the method, and to determine the most favorable protocols to follow in order to efficiently quantify multi-phase mixtures. Four sets of borehole samples of disposed or utilized CCBs were retrieved and analyzed by RQXRD according to the protocols developed under the first objective. The first set of samples, from a Class F ash settling pond in Kentucky disposed for up to 20 years, showed little mineralogical alteration, as expected. The second set of samples, from an embankment in Indiana containing a mixture of chain-grate (stoker) furnace ash and fluidized bed combustion (FBC) residues, showed formation of the mineral thaumasite, as observed in previously studied exposed FBC materials. Two high-calcium CCBs studied, including a dry-process flue gas desulfurization

  19. Advanced treatment of biologically pretreated coal gasification wastewater by a novel integration of three-dimensional catalytic electro-Fenton and membrane bioreactor.

    Science.gov (United States)

    Jia, Shengyong; Han, Hongjun; Hou, Baolin; Zhuang, Haifeng

    2015-12-01

    Laboratorial scale experiments were conducted to investigate a novel system three-dimensional catalytic electro-Fenton (3DCEF, catalyst of sewage sludge based activated carbon which loaded Fe3O4) integrating with membrane bioreactor (3DCEF-MBR) on advanced treatment of biologically pretreated coal gasification wastewater. The results indicated that 3DCEF-MBR represented high efficiencies in eliminating COD and total organic carbon, giving the maximum removal efficiencies of 80% and 75%, respectively. The integrated 3DCEF-MBR system significantly reduced the transmembrane pressure, giving 35% lower than conventional MBR after 30 days operation. The enhanced hydroxyl radical oxidation and bacteria self repair function were the mechanisms for 3DCEF-MBR performance. Therefore, the integrated 3DCEF-MBR was expected to be the promising technology for advanced treatment in engineering applications.

  20. DEVELOPMENT OF CONSTRUCTION OF A CATALYTIC REACTOR FOR METHANE OXIDISING IN VENTILATION AIR IN COAL MINES AND THE RESEARCH ON INTEGRATED “HEAT PIPE” RECUPERATOR

    Directory of Open Access Journals (Sweden)

    Lech Hys

    2013-04-01

    Full Text Available The article presents the analysis whose result is the selection of appropriate design and construction of a monolithic CMR reactor intended for oxidising methane from ventilation air in coal mines. The description of “heat-pipe” recuperator cooperating with the reactor was also presented. The research was mainly aimed at verifying the compliance with the work of autothermity premise obtained by the return of part of heat from catalytic reaction. The result of research was to define the range volumetric fume expense ensuring autothermity and the definition of maximum recuperator efficiency. The range of volumetric expense was 18–25 m3/h and maximum value of efficiency coefficient was η = 0.50 for the volumetric expense of 18 m3/h.

  1. Effect of the Sequence of the Thermoelectric Generator and the Three-Way Catalytic Converter on Exhaust Gas Conversion Efficiency

    Science.gov (United States)

    Su, Chuqi; Tong, Naiqiang; Xu, Yuman; Chen, Shan; Liu, Xun

    2013-07-01

    The potential for thermoelectric exhaust heat recovery in vehicles has increased with recent improvements in the efficiency of thermoelectric generators (TEGs). The problem with using thermoelectric generators for vehicle applications is whether the device is compatible with the original vehicle exhaust system, which determines the quality of the exhaust gas treatment and the realization of energy conservation and emission reduction. Based on ANSYS CFX simulation analysis of the impact of two positional relationships between the TEG and three-way catalytic converter in the exhaust system on the working efficiency of both elements, it is concluded that the layout with the front three-way catalytic converter has an advantage over the other layout mode under current conditions. New ideas for an improvement program are proposed to provide the basis for further research.

  2. The Role of Ruthenium in CO2 Capture and Catalytic Conversion to Fuel by Dual Function Materials (DFM

    Directory of Open Access Journals (Sweden)

    Shuoxun Wang

    2017-03-01

    Full Text Available Development of sustainable energy technologies and reduction of carbon dioxide in the atmosphere are the two effective strategies in dealing with current environmental issues. Herein we report a Dual Function Material (DFM consisting of supported sodium carbonate in intimate contact with dispersed Ru as a promising catalytic solution for combining both approaches. The Ru-Na2CO3 DFM deposited on Al2O3 captures CO2 from a flue gas and catalytically converts it to synthetic natural gas (i.e., methane using H2 generated from renewable sources. The Ru in the DFM, in combination with H2, catalytically hydrogenates both adsorbed CO2 and the bulk Na2CO3, forming methane. The depleted sites adsorb CO2 through a carbonate reformation process and in addition adsorb CO2 on its surface. This material functions well in O2- and H2O-containing flue gas where the favorable Ru redox property allows RuOx, formed during flue gas exposure, to be reduced during the hydrogenation cycle. As a combined CO2 capture and utilization scheme, this technology overcomes many of the limitations of the conventional liquid amine-based CO2 sorbent technology.

  3. Catalytic conversion of light alkanes-proof-of-concept stage - Phase IV. Topical report, February 1, 1994--January 31, 1995

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1998-12-31

    This report details the research performed on Phase IV of the extended Cooperative Agreement. This Phase, entitled C{sub 1}-C{sub 4} Research, provides the research support which accompanies the C{sub 4} Proof-of-Concept Phase (Phase V) as the two major activities of the Cooperative Agreement during calendar 1993. It is the objective of this phase to understand the nature of the catalysts and catalytic activity of perhaloporphyrin complexes uncovered during Phases I-III in order that superior catalytic materials can be made and tested which meet commercial criteria for the oxidation of the C{sub 1}-C{sub 4} light alkane gases found in natural gas and other available hydrocarbon streams. During Phase IV, we have examined the physical and electronic structures of the very active perhaloporphyrin catalysts which we have developed, and have gained an understanding of the properties which make them active. This has led us to design and synthesize materials which are cheaper, more active, more robust and, in general superior for carrying out practical catalysis. Our early generation perhaloporphyrin catalysts, while exhibiting unprecedented catalytic activity, were far too expensive for use in converting natural gas or its C{sub 1}-C{sub 4} components.

  4. Status and perspectives of CO2 conversion into fuels and chemicals by catalytic, photocatalytic and electrocatalytic processes

    NARCIS (Netherlands)

    Kondratenko, E.V.; Mul, G.; Baltrusaitis, J.; Larrazábal, G.O.; Pérez-Ramírez, J.

    2013-01-01

    This review highlights recent developments and future perspectives in carbon dioxide usage for the sustainable production of energy and chemicals and to reduce global warming. We discuss the heterogeneously catalysed hydrogenation, as well as the photocatalytic and electrocatalytic conversion of CO2

  5. Wyoming coal-conversion project. Final technical report, November 1980-February 1982. [Proposed WyCoalGas project, Converse County, Wyoming; contains list of appendices with title and identification

    Energy Technology Data Exchange (ETDEWEB)

    None

    1982-01-01

    This final technical report describes what WyCoalGas, Inc. and its subcontractors accomplished in resolving issues related to the resource, technology, economic, environmental, socioeconomic, and governmental requirements affecting a project located near Douglas, Wyoming for producing 150 Billion Btu per day by gasifying sub-bituminous coal. The report summarizes the results of the work on each task and includes the deliverables that WyCoalGas, Inc. and the subcontractors prepared. The co-venturers withdrew from the project for two reasons: federal financial assistance to the project was seen to be highly uncertain; and funds were being expended at an unacceptably high rate.

  6. Comparative Study of the Catalytic Activities of Three Distinct Carbonaceous Materials through Photocatalytic Oxidation, CO Conversion, Dye Degradation, and Electrochemical Measurements

    Science.gov (United States)

    Lee, Hangil; Kim, Yeonwoo; Kim, Min Ji; Kim, Ki-jeong; Kim, Byung-Kwon

    2016-01-01

    In order to compare the catalytic activities of reduced graphene oxide (rGO), graphene oxide (GO), and graphene, we conducted oxidation of 2-aminothiophenol (2-ATP) and reduction of nitrobenzene (NB) in their presence by using high-resolution photoemission spectroscopy (HRPES). In addition, we determined conversion rates of CO to CO2 in the presence of these catalysts by performing a residual gas analyzer (RGA) under a UHV condition, Orange II and methylene blue degradations UV-vis spectrophotometry, and electrochemistry (EC) measurements in an aqueous solution, as well as by obtaining cyclic voltammograms and determining the change of the condition of electrodes before and after the oxidation of 2-ATP. We found that we can successively fabricate GO (oxidation) and graphene (reduction) from rGO by controlling the oxidation or reduction procedure time and then clearly comparing the critical properties among them as we perform various oxidation and reduction activities. PMID:27762289

  7. Comparative Study of the Catalytic Activities of Three Distinct Carbonaceous Materials through Photocatalytic Oxidation, CO Conversion, Dye Degradation, and Electrochemical Measurements

    Science.gov (United States)

    Lee, Hangil; Kim, Yeonwoo; Kim, Min Ji; Kim, Ki-Jeong; Kim, Byung-Kwon

    2016-10-01

    In order to compare the catalytic activities of reduced graphene oxide (rGO), graphene oxide (GO), and graphene, we conducted oxidation of 2-aminothiophenol (2-ATP) and reduction of nitrobenzene (NB) in their presence by using high-resolution photoemission spectroscopy (HRPES). In addition, we determined conversion rates of CO to CO2 in the presence of these catalysts by performing a residual gas analyzer (RGA) under a UHV condition, Orange II and methylene blue degradations UV-vis spectrophotometry, and electrochemistry (EC) measurements in an aqueous solution, as well as by obtaining cyclic voltammograms and determining the change of the condition of electrodes before and after the oxidation of 2-ATP. We found that we can successively fabricate GO (oxidation) and graphene (reduction) from rGO by controlling the oxidation or reduction procedure time and then clearly comparing the critical properties among them as we perform various oxidation and reduction activities.

  8. H3PO4/Al2O3 catalysts: characterization and catalytic evaluation of oleic acid conversion to biofuels and biolubricant

    Directory of Open Access Journals (Sweden)

    Lucia Regina Raddi de Araujo

    2006-06-01

    Full Text Available Al2O3 and H3PO4/Al2O3 catalysts were investigated in the conversion of oleic acid to biofuels and biolubricant at 1 atm and at 623 K. The catalytic tests were performed in a fixed bed and continuous flow reactor, using an oleic acid-catalyst ratio of 4 and N2 as the carrier gas. The reaction products were analyzed by gas chromatography and acidity measurements. N2 adsorption-desorption, X ray diffraction, 31P nuclear magnetic resonance and FT-IR spectroscopy were also employed to evaluate the textural, structural and acidic properties of the catalysts. The results showed that phosphoric acid impregnation improved the alumina decarboxylation activities, generating hydrocarbons in the range of gasoline, diesel oil and lubricant oil. The best catalytic performance was achieved with the highest surface area alumina impregnated with H3PO4, which was the solid that allied high total acidity with a large quantity of mesopores.

  9. Green synthesis of gold and silver nanoparticles using gallic acid: catalytic activity and conversion yield toward the 4-nitrophenol reduction reaction

    Science.gov (United States)

    Park, Jisu; Cha, Song-Hyun; Cho, Seonho; Park, Youmie

    2016-06-01

    In the present report, gallic acid was used as both a reducing and stabilizing agent to synthesize gold and silver nanoparticles. The synthesized gold and silver nanoparticles exhibited characteristic surface plasmon resonance bands at 536 and 392 nm, respectively. Nanoparticles that were approximately spherical in shape were observed in high-resolution transmission electron microscopy and atomic force microscopy images. The hydrodynamic radius was determined to be 54.4 nm for gold nanoparticles and 33.7 nm for silver nanoparticles in aqueous medium. X-ray diffraction analyses confirmed that the synthesized nanoparticles possessed a face-centered cubic structure. FT-IR spectra demonstrated that the carboxylic acid functional groups of gallic acid contributed to the electrostatic binding onto the surface of the nanoparticles. Zeta potential values of -41.98 mV for the gold nanoparticles and -53.47 mV for the silver nanoparticles indicated that the synthesized nanoparticles possess excellent stability. On-the-shelf stability for 4 weeks also confirmed that the synthesized nanoparticles were quite stable without significant changes in their UV-visible spectra. The synthesized nanoparticles exhibited catalytic activity toward the reduction reaction of 4-nitrophenol to 4-aminophenol in the presence of sodium borohydride. The rate constant of the silver nanoparticles was higher than that of the gold nanoparticles in the catalytic reaction. Furthermore, the conversion yield (%) of 4-nitrophenol to 4-aminophenol was determined using reversed-phase high-performance liquid chromatography with UV detection at 254 nm. The silver nanoparticles exhibited an excellent conversion yield (96.7-99.9 %), suggesting that the synthesized silver nanoparticles are highly efficient catalysts for the 4-nitrophenol reduction reaction.

  10. Catalytic and Noncatalytic Conversion of Methane to Olefins and Synthesis Gas in an AC Parallel Plate Discharge Reactor

    Directory of Open Access Journals (Sweden)

    Mohammad Ali Khodagholi

    2013-01-01

    Full Text Available Direct conversion of methane to ethylene, acetylene, and synthesis gas at ambient pressure and temperature in a parallel plate discharge reactor was investigated. The experiments were carried out using a quartz reactor of outer diameter of 9 millimeter and a driving force of ac current of 50 Hz. The input power to the reactor to establish a stable gas discharge varied from 9.6 to maximum 15.3 watts (w. The effects of ZSM5, Fe–ZSM5, and Ni–ZSM5 catalysts combined with corona discharge for conversion of methane to more valued products have been addressed. It was found that in presence or absence of a catalyst in gas discharge reactor, the rate of methane and oxygen conversion increased upon higher input power supplied to the reactor. The effect of Fe–ZSM5 catalyst combined with gas discharge plasma yields C2 hydrocarbons up to 21.9%, which is the highest productions of C2 hydrocarbons in this work. The effect of combined Ni–ZSM5 and gas discharge plasma was mainly production of synthesis gas. The advantage of introducing ZSM5 to the plasma zone was increase in synthesis gas and acetylene production. The highest energy efficiency was 0.22 mmol/kJ, which belongs to lower rate of energy injection to the reactor.

  11. Catalytic conversion of light alkanes-proof-of-concept stage -- Phase 6. Final report, February 1--October 31, 1994

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1994-12-31

    During the course of the first three years of the Cooperative Agreement, the authors uncovered a family of metal perhaloporphyrin complexes which had unprecedented activity for the selective air-oxidation of light alkanes to alcohols. The reactivity of light hydrocarbon substrates with air or oxygen was in the order: isobutane > propane > ethane > methane, in accord with their homolytic bond dissociation energies. Isobutane was so reactive that the proof-of-concept stage of a process for producing tert-butyl alcohol from isobutane was begun (Phase 5). It was proposed that as more active catalytic systems were developed (Phases 4, 6), propane, then ethane and finally methane oxidations will move into this stage (Phases 7 through 9). As of this writing, however, the program has been terminated during the later stages of Phase 5 and 6 so that further work is not anticipated. 72 refs.

  12. Technical data. Final technical report, November 1980-May 1982. [Proposed WyCoalGas project, Converse County, Wyoming

    Energy Technology Data Exchange (ETDEWEB)

    None

    1982-01-01

    This volume includes a description of the railway to transport the coal; possible unbalance in the electrical power supply is considered in detail, as well as communications, signalling, etc. The railway will also be used to transport ashes and sludges for waste disposal. Coal fines in the coal supply will be burned to generate power. A very brief description of the coal gasification plant and its components is accompanied by a printout of the dates final engineering is to be completed. Permit applications are listed and socio-economic factors are discussed. The financing plan is discussed in some detail: basically, a loan guarantee from the Synthetic Fuels Corporation; equity provided by investment tax credit, deferred taxes, AFUDC and the sponsors; price support; and gas purchase agreement (this whole section includes several legal details.). (LTN)

  13. Coal liquefaction. Quarterly report, April-June 1979

    Energy Technology Data Exchange (ETDEWEB)

    None

    1980-04-01

    DOE's program for the conversion of coal to liquid fuels was begun by two of DOE's predecessor agencies: Office of Coal Research (OCR) in 1962, and Bureau of Mines, US Department of the Interior, in the 1930's. Current work is aimed at improved process configurations for both catalytic and non-catalytic processes to provide more attractive processing economics and lower capital investment. The advantage of coal liquefaction is that the entire range of liquid products, especially boiler fuel, distillate fuel oil, and gasoline, can be produced from coal by varying the type of process and operating conditions used in the process. Furthermore, coal-derived liquids have the potential for use as chemical feedstocks. To provide efficient and practical means of utilizing coal resources, DOE is supporting the development of several conversion processes that are currently in the pilot plant stage. DOE, together with the Electric Power Research Institue, has contracted with fourteen projects are described brieflly: funding, description, status, history, and progress in the current quarter. (LTN)

  14. Low temperature catalytic conversion of methane to formic acid by simple vanadium compound with use of H_2O_2

    Institute of Scientific and Technical Information of China (English)

    Xin Wei; Linmin Ye; Youzhu Yuan

    2009-01-01

    Selective oxidation of methane with hydrogen peroxide was catalyzed by several simple vanadium compounds in CH_3CN. The reaction could afford formic acid as the major product. Vanadyl oxysulfate (VOSO_4) was found to be an efficient catalyst. Specifically,the selectivity to formic acid of 70% at a methane conversion of 6.5% could be achieved over the VOSO_4 catalyst under the reaction conditions of methane pressure 3.0 MPa and temperature 333 K for 4 h. The UV-Vis spectroscopic measurements revealed that the formation of V~(5+) species during the reaction might be vital for the methane activation. The reaction probably proceeded via radical mechanism.

  15. Conversion and Estrogenicity of 17β-estradiol During Photolytic/Photocatalytic Oxidation and Catalytic Wet-air Oxidation.

    Science.gov (United States)

    Bistan, Mirjana; Tišler, Tatjana; Pintar, Albin

    2012-06-01

    Estrogen 17β-estradiol (E2), produced by human body and excreted into municipal wastewaters, belongs to the group of endocrine disrupting compounds that are resistant to biological degradation. The aim of this study was to assess the efficiency of E2 removal from aqueous solutions by means of catalytic wet-air oxidation (CWAO) and photolytic/photocatalytic oxidation. CWAO experiments were conducted in a trickle-bed reactor at temperatures up to 230 °C and oxygen partial pressure of 10 bar over TiO2 and Ru/TiO2 solids. Photolytic/photocatalytic oxidation was carried out in a batch slurry reactor employing a TiO2 P-25 (Degussa) catalyst under visible or UV light. HPLC analysis and yeast estrogen screen assay were used to evaluate the removal of E2 and estrogenicity of treated samples. The latter was completely removed during photolytic/photocatalytic oxidation under UV (365 nm) light and photocatalytic oxidation under visible light. In CWAO experiments, complete removal of both E2 and estrogenicity from the feed solution were noticed in the presence of TiO2 and Ru/TiO2 catalysts.

  16. Characterization and catalytic activity of NiO/mesoporous aluminosilicate AlSBA-15 in conversion of some hydrocarbons

    Directory of Open Access Journals (Sweden)

    Heba M. Gobara

    2012-06-01

    Full Text Available Mesoporous aluminosilicate AlSBA-15 was synthesized and adopted as a support for NiO with 3, 6 and 9 wt.% loadings. Characterization of various samples was performed through XRD, FTIR, DSC-TGA, TPR, SEM and TEM techniques. Textural and morphological characteristics were examined using N2 adsorption–desorption isotherms. Catalytic activities were measured in cumene cracking for parent AlSBA-15 and in n-hexane and toluene cracking and cyclohexane dehydrogenation for supported NiO samples. Uniformity of the ordered 2D-hexagonal structure of AlSBA-15 was evident even after loading with NiO. NiO and NiOOH phases could be detected particularly in the sample containing 9 wt.% NiO. TPR profile of solid loaded with 3 wt.% NiO sample showed negative peaks at 400 and 600 °C, related to hydrogen spillover on reduced sample. Selectivity towards n-hexane and toluene cracking increased with both temperature and metal oxide loading, achieving 100% at 350 °C. In cyclohexane dehydrogenation, the sample loaded with 3 wt.% NiO was the most active and selective one towards benzene formation.

  17. Catalytic conversion of xylose and corn stalk into furfural over carbon solid acid catalyst in γ-valerolactone.

    Science.gov (United States)

    Zhang, Tingwei; Li, Wenzhi; Xu, Zhiping; Liu, Qiyu; Ma, Qiaozhi; Jameel, Hasan; Chang, Hou-min; Ma, Longlong

    2016-06-01

    A novel carbon solid acid catalyst was synthesized by the sulfonation of carbonaceous material which was prepared by carbonization of sucrose using 4-BDS as a sulfonating agent. TEM, N2 adsorption-desorption, elemental analysis, XPS and FT-IR were used to characterize the catalyst. Then, the catalyst was applied for the conversion of xylose and corn stalk into furfural in GVL. The influence of the reaction time, temperature and dosage of catalyst on xylose dehydration were also investigated. The Brønsted acid catalyst exhibited high activity in the dehydration of xylose, with a high furfural yield of 78.5% at 170°C in 30min. What's more, a 60.6% furfural yield from corn stalk was achieved in 100min at 200°C. The recyclability of the sulfonated carbon catalyst was perfect, and it could be reused for 5times without the loss of furfural yields.

  18. Demonstration of selective catalytic reduction (SCR) technology for the control of nitrogen oxide (NO{sub x}) emissions from high-sulfur coal-fired boilers. Quarterly report No. 4, April--June 1991

    Energy Technology Data Exchange (ETDEWEB)

    1991-08-01

    The objective of this project is to demonstrate and evaluate commercially available Selective Catalytic Reduction (SCR) catalysts from US, Japanese and European catalyst suppliers on a high-sulfur US coal-fired boiler. SCR is a post-combustion nitrogen oxide (NOx) control technology that involves injecting ammonia into the flue gas generated from coal combustion in an electric utility boiler. The flue gas containing ammonia is then passed through a reactor that contains a specialized catalyst. In the presence of the catalyst, the ammonia reacts with NOx to convert it to nitrogen and water vapor, Although SCR is widely practiced in Japan and Europe, there are numerous technical uncertainties associated with applying SCR to US coals. These uncertainties include: (1) potential catalyst deactivation due to poisoning by trace metal species present in US coals that are not present in other fuel performance of the technology and effects on the balance-of-plant equipment in the presence of high amounts of SO{sub 2} and SO{sub 3}. (3) performance of a wide variety of SCR catalyst compositions, geometries and methods of manufacture under typical high-sulfur coal-fired utility operating conditions. These uncertainties will be explored by constructing a series of small-scale SCR reactors and simultaneously exposing different SCR catalysts to flue gas derived from the combustion of high sulfur US coal.

  19. Demonstration of selective catalytic reduction (SCR) technology for the control of nitrogen oxide (NO{sub x}) emissions from high-sulfur coal-fired boilers. Quarterly report No. 8, April--June, 1992

    Energy Technology Data Exchange (ETDEWEB)

    1992-08-01

    The objective of this project is to demonstrate and evaluate commercially available Selective Catalytic Reduction (SCR) catalysts from US, Japanese and European catalyst suppliers on a high-sulfur US coal-fired boiler. SCR is a post-combustion nitrogen oxide (NO{sub x}) control technology that involves injecting ammonia into the flue gas generated from coal combustion in an electric utility boiler. The flue gas containing ammonia is then passed through a reactor that contains a specialized catalyst. In the presence of the catalyst, the ammonia reacts with NO{sub x} to convert it to nitrogen and water vapor. Although SCR is widely practiced in Japan and Europe, there are numerous technical uncertainties associated with applying SCR to US coals. These uncertainties include: (1) potential catalyst deactivation due to poisoning by trace metal species present in US coals that are not present in other fuels. (2) performance of the technology and effects on the balance-of-plant equipment in the presence of high amounts of SO{sub 2} and SO{sub 3}. (3) performance of a wide variety of SCR catalyst compositions, geometries and methods of manufacture under typical high-sulfur coal-fired utility operating conditions. These uncertainties will be explored by constructing a series of small-scale SCR reactors and simultaneously exposing different SCR catalysts to flue gas derived from the combustion of high sulfur U. S. coal.

  20. Direct catalytic conversion of methane and light hydrocarbon gases. Quarterly report No. 6, January 16, 1988--April 15, 1988

    Energy Technology Data Exchange (ETDEWEB)

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

    1988-05-20

    The goal of this research is to develop catalysts that directly convert methane and light hydrocarbons to intermediates that later can be converted to either liquid fuels or value-added chemicals, as economics dictate. During this reporting period, we synthesized several phthalocyanine catalysts supported on magnesia (MgO) in Task 3. In Task 4 we have tested these catalysts for oxidation of methane and did a number of blank experiments to determine the cause of the low methanol yield we have observed. Magnesia supported catalysts were prepared by first synthesizing the various metal tetrasulfophthalocyanines (TSPCs), converting them to the acid form, and then supporting these complexes on a basic support (MgO) by a neutralization reaction. The metals used were Ru, Pd, Cu, Fe, Co, Mn, and Mo. CoTSPC was also synthesized in zeolite Y using our standard template techniques described in Quarterly Report No. 1. These complexes were examined for catalytic activity in the oxidation of methane. The PdTSPC/MgO had greater activity, and oxidized some of the methane (selectivity of 2.8% from the methane oxidized at 375{degrees}C) to ethane. This is a much lower temperature for this reaction than previously reported in the literature. We also examined the reactivity of various components of the system in the oxidation of the product methanol. The reactor showed some activity for the oxidation of methanol to carbon dioxide. When zeolite or magnesia were added, this activity increased. The magnesia oxidized most of the methanol to carbon dioxide, while the zeolite reduced some of the methanol to hydrocarbons. With oxygen in the feed gas stream (i.e., the conditions of our methane oxidation), a very large fraction of the methanol was oxidized to carbon dioxide when passed over magnesia. From this, we can conclude that any methanol formed in the oxidation of methane would probably be destroyed very quickly on the catalyst bed.

  1. Co-Al Mixed Oxides Prepared via LDH Route Using Microwaves or Ultrasound: Application for Catalytic Toluene Total Oxidation

    Directory of Open Access Journals (Sweden)

    Eric Genty

    2015-05-01

    Full Text Available Co6Al2HT hydrotalcite-like compounds were synthesized by three different methods: co-precipitation, microwaves-assisted and ultrasound-assisted methods. The mixed oxides obtained after calcination were studied by several techniques: XRD, TEM, H2-TPR and XPS. They were also tested as catalysts in the reaction of total oxidation of toluene. The physico-chemical studies revealed a modification of the structural characteristics (surface area, morphology as well as of the reducibility of the formed mixed oxides. The solid prepared by microwaves-assisted synthesis was the most active. Furthermore, a relationship between the ratio of Co2+ on the surface, the reducibility of the Co-Al mixed oxide and the T50 in toluene oxidation was demonstrated. This suggests a Mars Van Krevelen mechanism for toluene total oxidation on these catalysts.

  2. The Strategic Thinking About Cultivation and Development of Clean-coal-Conversion Strategic Emerging Industry%培育与发展煤炭洁净转化战略性新兴产业的思考

    Institute of Scientific and Technical Information of China (English)

    张军

    2015-01-01

    The author analyzes from the perspective of strategic, growth and positive externalities of clean-coal-conversion industry fosters as strategic emerging industry. Moreover, focuses on the strategic position and potential market research of clean-coal-conversion industry about coal-to-methane, coal-to-liquid, coal-based polygeneration and coal associated scarce aluminum recycling. At last, the author puts forward the strategic advice of clean-coal-conversion as strategic emerging industry from the aspects of science and technology sup⁃port, fiscal policy, overall planning, water resources protection and protection of special clean-coal-conversion.%煤炭利用的根本是高效利用煤中有效元素,煤炭洁净转化是转变煤炭利用方式、推进煤炭全效利用的重要方向。文章从战略性、成长性、正外部性等角度,对煤炭洁净转化产业可培育成为战略性新兴产业进行了分析,重点研究了煤制甲烷、煤制液体燃料、煤基多联产和煤炭共伴生稀缺铝资源回收等煤炭洁净转化产业的战略地位和市场潜力。最后从科技支撑、财政政策、统筹规划、水资源保障和煤炭洁净转化特殊煤种保护等几个方面,提出了发展煤炭洁净转化战略性新兴产业的建议。

  3. Hydrogen and methoxy coadsorption in the computation of the catalytic conversion of methanol on the ceria (111) surface

    Science.gov (United States)

    Beste, Ariana; Overbury, Steven H.

    2016-06-01

    Methanol decomposition to formaldehyde catalyzed by the ceria (111) surface was investigated using the DFT + U method. Our results rationalize experimental temperature programmed desorption experiments on the fully oxidized surface. Particular attention was paid to the effect of coadsorption of methoxy and hydrogen on various aspects of the conversion process. This issue had been raised by the experimental observation of water desorption at low temperature removing hydrogen from the system. Within this context, we also investigated hydrogen diffusion on the ceria surface. The hydrogen/methoxy interaction on ceria was shown to be ionic regardless of separation distance. The barrier for dehydrogenation of methoxy using the ionic model system, where hydrogen is coadsorbed, is above 1 eV. This barrier becomes negligible if an incorrect neutral model without coadsorbed hydrogen is employed. While water formation from isolated surface hydrogen is unlikely at low temperature, the presence of coadsorbed methoxy reduces the reaction energy for water formation considerably. For the dehydrated surface, we observed that the preference of the electron to locate at the methoxy oxygen instead of the cerium atom results in a surface that does not contain Ce3 + ions, despite the existence of a vacancy.

  4. Preliminary technical data report: WyCoalGas project water system. Final technical report, November 1980-May 1982. [Proposed WyCoalGas project, Converse County, Wyoming

    Energy Technology Data Exchange (ETDEWEB)

    None

    1982-01-01

    The WyCoalGas, Inc. Proposed coal gasification plant site is approximately 16 miles north of Douglas, Wyoming, located generally in Sections 27 and 34, T35N, R70W of the sixth prinicpal meridian. The plant site is located in typical high plateau plains of central Wyoming. Climate in the area is typical of semi-arid central Wyoming and is subject to wide variations in temperature. Precipitation in the area averages about 14 inches per year, of which about 10 inches fall during the April-September irrigation season. Projected water requirements at the plant site are 6020 acre-feet per year. Since the proposed plant site is not near any major streams or rivers, water must be transported to it. Water will be supplied from four sources - two surface water and two groundwater. The two surface water sources are LaPrele Reservoir and flood flows from the North Platte River with a 1974 appropriations date. LaPrele Reservoir is located approximately 14 miles west of Douglas, Wyoming, and is shown on Figure A-1. Water will be released from LaPrele Reservoir and flow down LaPrele Creek to the North Platte River. Water from the North Platte River will be diverted at a point in Section 7 of T33N, R71W. The LaPrele water and excess water from the North Platte will be pumped from the river and stored in Panhandle Reservoir No. 1, which is also referred to as Combs Reservoir. A pipeline will convey water from Panhandle Reservoir No. 1 to the coal gasification plant site. The two groundwater sources are located north of Douglas and west of Douglas.

  5. Catalytic Conversion of Short-Chain Alcohols on Atomically Dispersed Au and Pd Supported on Nanoscale Metal Oxides

    Science.gov (United States)

    Wang, Chongyang

    With the development of technologies for cellulosic biomass conversion to fuels and chemicals, bio-alcohols are among the main alternative feedstocks to fossil fuels. The research pursued in my thesis was the investigation of gold and palladium as catalysts for the application of short aliphatic alcohols to hydrogen generation and value-added chemicals production. Specifically, selective methanol steam reforming and non-oxidative ethanol dehydrogenation to hydrogen and acetaldehyde were investigated in this thesis work. A major aim of the thesis was to develop atomically efficient catalysts with tuned surface chemistry for the desired reactions, using suitable synthesis methods. Methanol steam reforming (SRM) for hydrogen production has recently been investigated on gold catalysts to overcome the drawbacks of copper catalysts (deactivation, pyrophoricity). Previous work at Tufts University has shown that both CeO2 and ZnO are suitable supports for gold. In this thesis, nanoscale composite oxides ZnZrOx were prepared by a carbon hard-template method, which resulted in homogeneous distribution of Zn species in the matrix of ZrO2. Tunable surface chemistry of ZnZrO x was demonstrated by varying the Zn/Zr ratio to suppress the strong Lewis acidity of ZrO2, which leads to undesired production of CO through methanol decomposition. With atomic dispersion of gold, Au/ZnZrO x catalyzes the SRM reaction exclusively via the methanol self-coupling pathway up to 375°C. The activity of Au/ZnZrOx catalysts was compared to Au/TiO2, which is another catalyst system demonstrating atomic dispersion of gold. Similarity in the apparent activation energy of SRM on all the supported gold catalysts studied in this thesis and in the literature further confirms the same single-site Au-Ox-MO centers as active sites for SRM with indirect effects of the supports exploited. With this fundamental understanding of gold-catalyzed C1 alcohol reforming, the Au/ZnZrOx catalyst was evaluated for the

  6. Measurement and modeling of advanced coal conversion processes, Volume I, Part 2. Final report, September 1986--September 1993

    Energy Technology Data Exchange (ETDEWEB)

    Solomon, P.R.; Serio, M.A.; Hamblen, D.G. [and others

    1995-09-01

    This report describes work pertaining to the development of models for coal gasification and combustion processes. This volume, volume 1, part 2, contains research progress in the areas of large particle oxidation at high temperatures, large particle, thick-bed submodels, sulfur oxide/nitrogen oxides submodels, and comprehensive model development and evaluation.

  7. Coprocessing of coal and heavy petroleum crudes and residua: a solvent evaluation and a parametric study

    Energy Technology Data Exchange (ETDEWEB)

    Curtis, C.W.; Guin, J.A.; Tsai, K.J.; Pass, M.C.

    1984-01-01

    This study has investigated the combined hydroprocessing of coal with petroleum solvents consisting of heavy and reduced crudes and residua to determine the feasibility of simultaneous upgrading of both materials to lighter products. Six hydrogen-rich heavy petroleum materials have been processed with Illinois No. 6 coal at 400/sup 0/C and 425/sup 0/C for 30 minutes under three reaction conditions: a N/sub 2/ atmosphere, a H/sub 2/ atmosphere and a H/sub 2/ atmosphere using hydrotreating extrudates. Liquefaction of bituminous coal can be achieved in the petroleum solvents with coal conversion being dependent upon the reaction conditions. Noncatalytic coal conversions of 45 to 50% are achieved in a H/sub 2/ atmosphere. Addition of a catalyst increases conversion to near 70%. Only approximately 35% conversion is obtained in a N/sub 2/ atmosphere. In the catalytic environment substantial conversions to pentane soluble material occur. Hydrotreatment and extraction of the solvent prior to coprocessing increases the amount of coal conversion and, in some cases, increases the amount of pentane soluble material produced. The influence of the solvent appears to be related to the molecular weight, viscosity and Conradson Carbon number of the petroleum materials. Evaluation of the reaction parameters of temperature, hydrogen pressure, time and catalyst extrudate size for coprocessing has been undertaken. Based on the production of pentane soluble oil and coal conversion, feasible parameters are established: 425/sup 0/C, 1250 psig H/sub 2/ pressure at ambient temperature, long reaction time and a hydrogenation catalyst with a small particle size. Combined processing is shown to be sensitive to catalyst extrudate size, with powdered catalyst giving substantially more oil yield and coal conversion than the extrudates. 6 references, 11 figures, 4 tables.

  8. In situ FTIR spectroscopic assessment of methylbutynol catalytic conversion products in relation to the surface acid-base properties of systematically modified aluminas

    Science.gov (United States)

    Mekhemer, Gamal A. H.; Zaki, Mohamed I.

    2016-10-01

    The present investigation was designed to assess the credibility of methylbutynol (MBOH) as an infrared (IR) reactive probe molecule for surface acid-base properties of metal oxides. Accordingly, pure alumina was systematically modified with varied amounts (0.5-10 wt.%) of K+ or SO42 - additives. Then, the influence of nature and amount of the additive on the following alumina properties were examined: (i) bulk composition and structure by X-ray powder diffractometry and ex-situ IR spectroscopy, (ii) surface area and net charge by N2 sorptiometry and pH-metry, respectively, and (iii) nature and strength of exposed surface acid sites by in-situ IR spectroscopy of adsorbed pyridine at ambient and higher temperatures. Results obtained were correlated with IR-identified product distribution of MBOH catalytic decomposition/conversion at 200 °C. It is thereby concluded that MBOH is superior to conventional IR inactive probe molecules in gauging sensitively the prevailing acid or base character, availability of base sites, relative population of Bronsted to Lewis acid sites, and strength and reactivity of the sites exposed on metal oxide surfaces. Hence, all that is needed to get this information is to handle IR spectra taken from the gas phase, a task that is experimentally much more accessible than taking spectra from adsorbed species of irreactive probe molecules.

  9. Demonstration of Selective Catalytic Reduction (SCR) technology for the control of nitrogen oxide (NO{sub x}) emissions from high-sulfur coal-fired boilers. Technical progress report, first and second quarters 1994

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1995-11-01

    The objective of this project is to demonstrate and evaluate commercially available Selective Catalytic Reduction (SCR) catalysts from U.S., Japanese and European catalyst suppliers on a high-sulfur U.S. coal-fired boiler. SCR is a post-combustion nitrogen oxide (NO{sub x}) control technology that involve injecting ammonia into the flue gas generated from coal combustion in a boiler. The flue gas containing ammonia is then passed through a reactor that contains a specialized catalyst. In the presence of the catalyst, the ammonia reacts with NO{sub x} to form nitrogen and water vapor. Although SCR is widely practiced in Japan and Europe on gas-, oil-, and low-sulfur coal-fired boilers, there are several technical uncertainties associated with applying SCR to U.S. coals. These uncertainties include: (1) potential catalyst deactivation due to poisoning by trace metal species present in U.S. coals that are not present in other fuels; (2) performance of the technology and effects on the balance-of-plant equipment in the presence of high amounts of SO{sub 2} and SO{sub 3}; and (3) performance of a wide variety of SCR catalyst compositions, geometries and methods of manufacture under typical high-sulfur coal-fired utility operating conditions. These uncertainties are being explored by operating a series of small-scale SCR reactors and simultaneously exposing different SCR catalysts to flue gas derived from the combustion of high sulfur U.S. coal. The project is being conducted in the following three phases: permitting, environmental monitoring plan and preliminary engineering; detailed design engineering and construction; and operation, testing, disposition and final report. The project was in the operation and testing phase during this reporting period. Accomplishments for this period are described.

  10. Innovative clean coal technology (ICCT): demonstration of selective catalytic reduction (SCR) technology for the control of nitrogen oxide (NO{sub x}) emission from high-sulfur, coal-fired boilers - economic evaluation of commercial-scale SCR applications for utility boilers

    Energy Technology Data Exchange (ETDEWEB)

    Healy, E.C.; Maxwell, J.D.; Hinton, W.S.

    1996-09-01

    This report presents the results of an economic evaluation produced as part of the Innovative Clean Coal Technology project, which demonstrated selective catalytic reduction (SCR) technology for reduction of NO{sub x} emissions from utility boilers burning U.S. high-sulfur coal. The document includes a commercial-scale capital and O&M cost evaluation of SCR technology applied to a new facility, coal-fired boiler utilizing high-sulfur U.S. coal. The base case presented herein determines the total capital requirement, fixed and variable operating costs, and levelized costs for a new 250-MW pulverized coal utility boiler operating with a 60-percent NO{sub x} removal. Sensitivity evaluations are included to demonstrate the variation in cost due to changes in process variables and assumptions. This report also presents the results of a study completed by SCS to determine the cost and technical feasibility of retrofitting SCR technology to selected coal-fired generating units within the Southern electric system.

  11. Cooperative research program in coal liquefaction. Quarterly report, August 1, 1991--October 31, 1991

    Energy Technology Data Exchange (ETDEWEB)

    Huffman, G.P. [ed.

    1991-12-31

    This Quarterly Report on coal liquefaction research includes discussion in the areas of (1) Iron Based Catalysts for Coal Liquefaction; (2) Exploratory Research on Coal Conversion; (3) Novel Coal Liquefaction Concepts; (4) Novel Catalysts for Coal Liquefaction. (VC)

  12. Influence of reaction parameters on brown coal-polyolefinic plastic co-pyrolysis behavior

    Energy Technology Data Exchange (ETDEWEB)

    Sharypov, V.I.; Beregovtsova, N.G.; Kuznetsov, B.N. [Institute of Chemistry and Chemical Technology SB RAS, K.Marx Str. 42, 660049 Krasnoyarsk (Russian Federation); Cebolla, V.L. [Instituto de Carboquimica, CSIC, Miguel Luesma, 4, 50015 Zaragoza (Spain); Collura, S.; Finqueneisel, G.; Zimny, T.; Weber, J.V. [Laboratoire de Chimie et Applications, Universite de Metz, rue V.Demange, 57500 Saint-Avold (France)

    2007-03-15

    Co-processing of polyolefinic polymers with Kansk-Achinsk (Russia) brown coal was investigated by thermogravimetry (TG) and autoclave pyrolysis under argon and hydrogen pressure in catalytic conditions (or not). Gas chromatography-mass spectrometry (GC-MS) and high performance thin layer chromatography (HPTLC) were used to analyze the distillate products. Some synergistic effects indicate chemical interaction between the products of thermal decomposition of coal and plastic. In co-pyrolysis under H{sub 2} a significant increasing of coal conversion degree as a function of polymer amount in feedstock was found. Simultaneously the coal promoted formation of distillate products from polymers. Some alkyl aromatic and O-containing substances were detected in co-pyrolysis fraction boiling in the range 180-350 C, indicating interactions between coal and plastic. Iron containing ore materials, modified by mechanochemical treatment, demonstrated a catalytic activity in hydropyrolysis process. In catalytic conditions, increases of the mixtures conversion degree by 9-13 wt.%, of distillate fraction yields by 1.2-1.6 times and a decrease of olefins and polycyclic components were observed. (author)

  13. Research Progress in Catalytic Oxidation Technology for Coal Chemical Industry Wastewater%催化氧化技术处理煤化工废水研究进展

    Institute of Scientific and Technical Information of China (English)

    王晓雷

    2015-01-01

    Several catalytic oxidation technology for coal chemical wastewater treatment research status and the advantages and disadvantages are described and compared,some suggestions about furtul methods, and fur⁃ther researchare proposed.%针对几种催化氧化技术处理煤化工废水的研究现状进行了评述和比较,分析了各种技术的优缺点,对今后研究方向提出了建议。

  14. Application of a validated gasification model to determine the impact of coal particle grinding size on carbon conversion

    KAUST Repository

    Kumar, Mayank

    2013-06-01

    In this paper, we describe the implementation of a comprehensive, previously validated multiscale model of entrained flow gasification to examine the impact of particle size on the gasification process in two different gasifier designs; the MHI and the GE gasifier. We show that the impact of the particle size depends on whether the char conversion process is kinetically limited or boundary layer diffusion-limited. Fine grinding helps accelerate char conversion under diffusion-control conditions, whereas the impact is not as noticeable under kinetic-control operation. The availability of particular gasification agents, namely O2 in the earlier sections of the gasifier or CO2 and H2O in the latter sections, as well as the temperature, are shown to have an impact on the relative importance of kinetics versus diffusion limitation. © 2013 Elsevier Ltd. All rights reserved.

  15. Metal-oxide-catalyzed CO{sub 2} gasification of coal using a solar furnace simulator

    Energy Technology Data Exchange (ETDEWEB)

    Kodama, T.; Funatoh, A.; Shimizu, T.; Kitayama, Y. [Niigata University, Niigata (Japan). Department of Chemistry & Chemical Engineering, Faculty of Engineering

    2000-12-01

    Metal-oxide-catalyzed CO{sub 2} gasification of coal was demonstrated in small packed-bed and fluidized-bed reactors using a solar furnace simulator, for the purpose of converting solar high-temperature heat to chemical fuels. The catalytic activities of In{sub 2}O{sub 3} and ZnO were investigated because used In{sub 2}O{sub 3} or ZnO catalyst may be separated from remaining coal ash by In{sub 2}O{sub 3} and Zn evaporation at high temperatures and at a reducing atmosphere. Bituminous coal with or without the metal-oxide catalyst in the quartz-tube reactor was directly irradiated by the concentrated Xe-lamp beam and CO{sub 2} was fed to the reactor at pCO{sub 2} = 1.0. In the packed-bed reactor, In{sub 2}O{sub 3} and ZnO much improved the chemical coal conversion by about 4-5 and 2-3 times at the catalyst loading of 17 wt%-In and 30 wt %-Zn in the coal-metal-oxide mixture, respectively, at temperatures around 1000-1400 K. In the fluidized-bed reactor at a small catalyst loading (8-10 wt%-metal in the coal-metal-oxide mixture) and at 1073-1163 K, In{sub 2}O{sub 3} catalytically increased the coal-conversion rate by 3 times but ZnO scarcely showed the catalytic activity. This metal-catalyzed coal gasification process offers the efficient solar production of the syngas calorifically upgraded by solar energy. 24 refs., 11 figs., 3 tabs.

  16. 煤制芳香化合物的探讨%Investigation on Preparation of Aromatic Compounds from Coal

    Institute of Scientific and Technical Information of China (English)

    王德海; 常丽萍

    2011-01-01

    This paper commented on the latest development of the coal pyrolysis, catalytic conversion and the technology of abstracting high value-added aromatic compounds from coal. Based on relevant researches home and abroad, the paper laid emphasis on discussing the technology of coal pyrolysis and coal hydro liquefaction for abstracting aromatic chemicals including such technologies as coal rapid pyrolysis and directional catalytic conversion technology of the coal pyrolysate. A new approach of producing high value-added aromatic product from coal was put forward.%综述了国内外两种煤制芳香化学品技术的研究现状,一种为煤热解制芳香化学品,包括煤快速热解和煤热解物定向催化转化技术;另一种为煤加氢液化制芳香化学品技术.今后在加强煤制芳香化学品研究的同时,还应加强对煤液化产品分离技术的研究.

  17. Influence of Gas Feed Composition and Pressure on the Catalytic Conversion of CO2 to Hydrocarbons Using a Traditional Cobalt-Based Fischer-Tropsch Catalyst

    Science.gov (United States)

    2009-06-25

    availability. Fuel independence would alleviate uncertainties in the world market supply of oil along with commercial fluctuations in price. In addition...this supply by supporting the development of synthetic hydrocarbon fuel from the vast natural resources, such as coal, shale, gas hydrates, and CO2...product a day by steam-reforming coal to generate syngas for the FT process.5 A water-gas shift is needed to obtain a 2:1 ratio of hydrogen/carbon

  18. Pyrolysis of Coal

    Directory of Open Access Journals (Sweden)

    Rađenović, A.

    2006-07-01

    Full Text Available The paper presents a review of relevant literature on coal pyrolysis.Pyrolysis, as a process technology, has received considerable attention from many researchers because it is an important intermediate stage in coal conversion.Reactions parameters as the temperature, pressure, coal particle size, heating rate, soak time, type of reactor, etc. determine the total carbon conversion and the transport of volatiles and therebythe product distribution. Part of the possible environmental pollutants could be removed by optimising the pyrolysis conditions. Therefore, this process will be subsequently interesting for coal utilization in the future

  19. Method and apparatus for conversion of carbonaceous materials to liquid fuel

    Energy Technology Data Exchange (ETDEWEB)

    Lux, Kenneth W.; Namazian, Mehdi; Kelly, John T.

    2015-12-01

    Embodiments of the invention relates to conversion of hydrocarbon material including but not limited to coal and biomass to a synthetic liquid transportation fuel. The invention includes the integration of a non-catalytic first reaction scheme, which converts carbonaceous materials into a solid product that includes char and ash and a gaseous product; a non-catalytic second reaction scheme, which converts a portion of the gaseous product from the first reaction scheme to light olefins and liquid byproducts; a traditional gas-cleanup operations; and the third reaction scheme to combine the olefins from the second reaction scheme to produce a targeted fuel like liquid transportation fuels.

  20. Pyrolysis and combustion behaviour of coal-MBM blends.

    Science.gov (United States)

    Skodras, G; Grammelis, P; Basinas, P

    2007-01-01

    In the present work, thermogravimetric analysis was employed in order to investigate the behaviour of MBM and their blends with Greek brown coal, under pyrolysis and combustion conditions. MBM presented enhanced pyrolysis rates reflecting its high volatile and low ash contents compared to Greek brown coal. Increased conversion rates were observed when MBM was added in the brown coal sample. Significant interactions were detected between the two fuel blend components leading to significant deviations from the expected behaviour. The catalytic effect of mineral matter on the pyrolysis of MBM resulted in reaction rate decrease and DTG curve shift to lower temperatures for the demineralised MBM. Alterations in the combustion process due to the mineral matter were minimal when testing the blends. Interactions maintained during combustion and lower reactivity of MBM was achieved due to the reduced oxygen content.

  1. Pyrolysis and combustion behaviour of coal-MBM blends

    Energy Technology Data Exchange (ETDEWEB)

    Skodras, G.; Grammelis, P.; Basinas, P. [Center for Research & Technology Hellas, Ptolemais (Greece)

    2007-01-15

    In the present work, thermogravimetric analysis was employed in order to investigate the behaviour of MBM (meat and bone meal) and their blends with Greek brown coal, under pyrolysis and combustion conditions. MBM presented enhanced pyrolysis rates reflecting its high volatile and low ash contents compared to Greek brown coal. Increased conversion rates were observed when MBM was added in the brown coal sample. Significant interactions were detected between the two fuel blend components leading to significant deviations from the expected behaviour. The catalytic effect of mineral matter on the pyrolysis of MBM resulted in reaction rate decrease and DTG curve shift to lower temperatures for the demineralised MBM. Alterations in the combustion process due to the mineral matter were minimal when testing the blends. Interactions maintained during combustion and lower reactivity of MBM was achieved due to the reduced oxygen content.

  2. Nickel-catalyzed hydroliquefaction of Morwell brown coal at low temperatures using phenolic compounds as solvents

    Energy Technology Data Exchange (ETDEWEB)

    Takemura, Y.; Saito, Y.; Okada, K.; Koinuma, Y.

    To attain a more effective coal liquefaction process, low-temperature (230-270 degrees C) coal hydroliquefaction was performed by using 15 kinds of single- or double-ring phenolic compounds as solvents and nickel acetate as a catalyst precursor. The role of the phenolic compound in the liquefaction reaction is discussed. With selected compounds, such as 1,7-dihydroxynaphthalene and resorcinol, Morwell brown coal was catalytically liquefied in a batch autoclave under H/sub 2/ pressure (10 MPa, cold) to give the coversions of the coal (to benzene/ethanol mixture solubles), which are higher than 70 wt%, at 270 degrees C for 1 h. Among three dihydroxybenzenes, resorcinol showed the highest efficiency for the Ni-catalyzed hydroliquefaction of the coal, though the capability of resorcinol to dissolve coal is the lowest in the absence of H/sub 2/. Capabilities of o-phenylphenol and its related compounds to dissolve the coal at 250 degrees C under Ar pressure (10 MPa, cold) and to hydroliquefy the coal at 270 degrees C under H/sub 2/ pressure (10 MPa, cold) were quantified. The respective orders of the conversion of the coal with these compounds are as follows: o-phenylphenol approximately equal to o-cyclohexylphenol > biphenyl approximately equal to cyclohexylbenzene. At this temperature, the solvent effect of phenolic functionality is larger than that of the hydroaromatic one. The same result is found with 1-naphthol and 5,6,7,8-tetrahydro-1-naphthol. 20 refs., 4 tabs.

  3. Liquid-metal MHD energy conversion. Status report, March 1976--September 1977. [Coal combustion products are mixed with liquid copper and act as working fluid

    Energy Technology Data Exchange (ETDEWEB)

    Petrick, M; Dunn, P F; Pierson, E S; Dauzvardis, P V; Pollack, I

    1979-05-01

    A new open-cycle coal-fired liquid-metal MHD concept has been developed, in which the combustion products are mixed directly with liquid copper and the mixture is then passed through the MHD generator. This concept yields a system with an efficiency comparable to that of open-cycle plasma MHD at combustor temperatures as much as 1000 K lower and MHD generator temperatures more than 1000 K lower than is the case for open-cycle plasma MHD. Significantly, the liquid-metal system uses components that are close to or within present-day technology, and it appears that readily available containment materials are compatible with the fluids. The first commercial system studies for the liquid-metal Rankine-cycle concept show that it yields a higher conversion efficiency than conventional steam cycles for lower-temperature heat sources, such as a liquid-metal fast-breeder reactor, a light-water reactor, or solar collectors without any potential for hazardous reactions betweeen liquid metals (e.g., sodium) and water. Fabrication of the high-temperature liquid-metal MHD facility has been completed, and shakedown runs have been performed, using a substitute mixer-generator test section. Data obtained in this test section agreed well with existing single-phase and newly-developed two-phase correlations for the pressure gradient.

  4. Abstracts of the first ORNL workshop on polycyclic aromatic hydrocarbons: characterization and measurement with a view toward personnel protection. [PAH from coal conversion

    Energy Technology Data Exchange (ETDEWEB)

    Gammage, R.B. (comp.)

    1976-11-01

    This report contains the abstracts of papers presented at a workshop on polycyclic aromatic hydrocarbons (PAH) such as those produced by coal conversion technologies. Their often carcinogenic nature imposes the obligation of providing adequate protection and measurement devices for workers and for the general public. The primary questions are as follows: What should be measured. Where and how should it be measured. What are the maximum permissible concentrations. This workshop and future workshops are intended to bring these problems into better focus and to help establish a consensus on what needs to be done in order to provide a dosimetry effort that will ensure the adequate protection of personnel. There were 32 attendees of this one-day meeting. The papers and discussions included current industrial hygiene practices, the development of government agency guidelines for worker protection, and a wide range of analytical techniques for PAH detection, some of which are still in the research stage and are unproven. The workshop was held at ORNL on February 26, 1976.

  5. The demonstration of an advanced cyclone coal combustor, with internal sulfur, nitrogen, and ash control for the conversion of a 23 MMBTU/hour oil fired boiler to pulverized coal

    Energy Technology Data Exchange (ETDEWEB)

    Zauderer, B.; Fleming, E.S.

    1991-08-30

    This work contains to the final report of the demonstration of an advanced cyclone coal combustor. Titles include: Chronological Description of the Clean Coal Project Tests,'' Statistical Analysis of Operating Data for the Coal Tech Combustor,'' Photographic History of the Project,'' Results of Slag Analysis by PA DER Module 1 Procedure,'' Properties of the Coals Limestone Used in the Test Effort,'' Results of the Solid Waste Sampling Performed on the Coal Tech Combustor by an Independent Contractor During the February 1990 Tests.'' (VC)

  6. Continuous coal processing method

    Science.gov (United States)

    Ryason, P. R.

    1980-06-01

    A coal pump is provided in which solid coal is heated in the barrel of an extruder under pressure to a temperature at which the coal assumes plastic properties. The coal is continuously extruded, without static zones, using, for example, screw extrusion preferably without venting through a reduced diameter die to form a dispersed spray. As a result, the dispersed coal may be continuously injected into vessels or combustors at any pressure up to the maximum pressure developed in the extrusion device. The coal may be premixed with other materials such as desulfurization aids or reducible metal ores so that reactions occur, during or after conversion to its plastic state. Alternatively, the coal may be processed and caused to react after extrusion, through the die, with, for example, liquid oxidizers, whereby a coal reactor is provided.

  7. Advanced bioreactor concepts for gaseous substrates: Conversion of synthesis gas to liquid fuels and removal of SO{sub x} and NO{sub x} from coal combustion gases. CRADA final report

    Energy Technology Data Exchange (ETDEWEB)

    Kaufman, E.N.; Selvaraj, P.T.

    1997-10-01

    The purpose of the proposed research program was the development and demonstration of a new generation of gaseous substrate-based bioreactors for the production of liquid fuels from coal synthesis gas and the removal of NO{sub x} and SO{sub x} species from coal combustion flue gas. This study addressed the further investigation of optimal bacterial strains, growth media and kinetics for the biocatalytic conversion of coal synthesis gas to liquid fuel such as ethanol and the reduction of gaseous flue gas constituents. The primary emphasis was on the development of advanced bioreactor systems coupled with innovative biocatalytic systems that will provide increased productivity under controlled conditions. It was hoped that this would result in bioprocessing options that have both technical and economic feasibility, thus, ensuring early industrial use. Predictive mathematical models were formulated to accommodate hydrodynamics, mass transport, and conversion kinetics, and provide the data base for design and scale-up. The program was separated into four tasks: (1) Optimization of Biocatalytic Kinetics; (2) Development of Well-mixed and Columnar Reactors; (3) Development of Predictive Mathematical Models; and (4) Industrial Demonstration. Research activities addressing both synthesis gas conversion and flue gas removal were conducted in parallel by BRI and ORNL respectively.

  8. Residues from coal conversion and utilization: Advanced mineralogical characterization and disposed byproduct diagenesis. [Semiannual report, 1 Mar 1999--31 Aug 1999

    Energy Technology Data Exchange (ETDEWEB)

    Gregory J. McCarthy; Dean G. Grier

    2000-01-01

    The goal of the project is to learn more about the phenomenon of coal conversion byproduct (CCB) diagenesis, first described by this group and co-workers at UND EERC seven years ago. CCB diagenesis is a change in the mineralogy that occurs after some CCBs are disposed in a landfill or utilized for a civil engineering application. Regulatory environmental tests and civil engineering tests are typically performed on as-generated CCBs, or on CCBs hydrated and cured for relatively short periods such as 7 or 28 days. One would like to know whether the results of these short-term tests will be valid years later. A change in mineralogy means a gain, loss or chemical redistribution of major, minor and trace elements, and alteration of physical properties. To attain this goal, two objectives were defined: (1) to develop improved methodology for quantitating mineralogy of these complex crystalline phase assemblages, and (2) to investigate the phenomenon of CCB diagenesis further by studying materials recovered from disposal landfills or civil engineering works. Objective 1--Hydrated CCBs are chemically and mineralogically complex, which makes quantitative mineralogy determination by conventional X-ray diffraction unusable or unreliable. The whole-pattern Rietveld quantitative X-ray diffraction (RQXRD) method, however, can overcome many of the problems and seems well suited to improve reliability. Two tasks were defined in the proposal: Task 1--Completion by October 1997. Prepare a reference set of CCBs for use in developing Rietveld QXRD. The reference materials will come primarily from in-house samples of advanced coal technology byproducts. The work will include SEM/EMPA characterization at UND EERC. Task 2--Completion by October 1997. Develop protocols for Rietveld QXRD analysis of CCBs. Make CCB structure data and protocols available on a Website. Determine levels of sensitivity, precision, and accuracy. Objective 2--Five types of CCBs disposed in landfills were studied

  9. Catalytic Conversion of Castor Oil to Biodiesel Using Ionic Liquid as Catalyst%碱性离子液体在制备生物柴油中的应用

    Institute of Scientific and Technical Information of China (English)

    马洁; 顾俊; 夏晓莉; 倪邦庆; 王海军

    2012-01-01

    Efficient catalytic conversion of castor oil to biodiesel,is achieved using 1-buthyl-3-methylimidazolium hydroxide(OH) as the catalyst.The influence factors,such as alcohol-oil ratio,catalyst dosage,reaction temperature,reaction time are investigated in detail.The results showed that OH was an efficient catalyst for catalytic conversion of castor oil to biodiesel,and 82.3 % yield of HMF was obtained for 90 min at 50 ℃ in the presence of the load of catalyst was 8 % and the CH3OH: oil ratio was 9∶1.%文章研究了碱性离子液体1-丁基-3-甲基咪唑氢氧盐([Bmim]OH)催化蓖麻油酯交换制备生物柴油的工艺。考察了醇油比、催化剂用量、反应温度、反应时间等因素对脂肪酸甲酯的得率的影响。研究表明以[Bmim]OH为催化剂,脂肪酸甲酯得率达到82.3%。最佳反应条件为:醇油摩尔比9∶1,催化剂用量8%,反应温度50℃,反应时间90 min。

  10. Hydrogen production from co-gasification of coal and biomass in supercritical water by continuous flow thermal-catalytic reaction system

    Institute of Scientific and Technical Information of China (English)

    YAN Qiuhui; GUO Liejin; LIANG Xing; ZHANG Ximin

    2007-01-01

    Hydrogen is a clean energy carrier.Converting abundant coal sources and green biomass energy into hydrogen effectively and without any pollution promotes environmental protection.The co-gasification performance of coal and a model compound of biomass,carboxymethylcellulose (CMC)in supercritical water (SCW),were investigated experimentally.The influences of temperature,pressure and concentration on hydrogen production from co-gasification of coal and CMC in SCW under the given conditions (20-25 MPa,650℃,15-30 s) are discussed in detail.The experimental results show that H2,CO2 and CH4 are the main gas products,and the molar fraction of hydrogen reaches in excess of 60%.The higher pressure and higher CMC content facilitate hydrogen production;production is decreased remarkably given a longer residence time.

  11. Pilot plant development of a new catalytic process for improved electrostatic separation of fly ash in coal-fired power plants

    Energy Technology Data Exchange (ETDEWEB)

    Olivares del Valle, J.; Martinez, L.S.; Baum, B.M.; Galeano, V.C. [Universidad de Sevilla (Spain)

    1995-12-31

    The design and operation of pulverized-coal-fired power plants (PCFPP) are usually regarded as fuel range in terms of sulphur and ash contents. These units may give severe environmental problems of fly ash emissions as a result of lower SO{sub 3} contents in the flue gas (FG) because the electrical resistivity of the solid particles is correspondingly lower, with consequent adverse effects on electrostatic precipitator (ESP) efficiency. More stringent air pollution laws cause many power companies to burn lower sulphur coal under boilers in plants that formerly burned higher S coal or ran with abnormal operational conditions (only remediable by shutdown and repairs). This presentation of the GASOX process is a contribution to the improvement of existing technology for flue gas conditioning (FGC), which is defined as a control system for (ESP) efficiency in PCFPP.

  12. Physicochemical Properties of Coal Gasification Slag and Its Catalytic Effect on Gasification Reactivity of Petroleum Coke%气化灰渣的理化性质及其对石油焦/CO_2气化反应特性的影响

    Institute of Scientific and Technical Information of China (English)

    平雅敏; 黄胜; 吴诗勇; 吴幼青; 高晋生

    2012-01-01

    The physicochemical properties of Shenhua coal gasification slag were characterized with the aids of XRF,XRD and SEM/EDS,and the catalytic effect of gasification slag on petroleum coke/CO2 gasification reactivity was also investigated.The results showed that the ash contents of bottom slag and fly ash were 78.39% and 62.71%,respectively.Bottom slag contained higher contents of Ca and Fe,but lower contents of Si and Al than those of fly ash.Inorganic matters in gasification slag mainly existed in the form of inert materials with no gasification reactivity.Calcium sulfate,iron oxide and glaserite(K3Na(SO4)2) in bottom slag were main catalytic components,while there was only low content of calcium sulfate in fly ash with catalytic effect.With increasing addition of slag,carbon conversion versus maximum gasification reactivity decreased.Catalytic gasification reactivity of petroleum coke with 5%-30% addition of gasification slag was raised 2-7 times as compared with non-catalytic one,and bottom slag had higher catalytic activity than fly ash.%采用XRF、XRD和SEM/EDS等分析手段对神华煤气化灰渣的理化性质进行了表征,并考察了气化灰渣对金山石油焦/CO2气化反应活性的影响。结果表明:炉底灰渣和炉顶飞灰的灰分质量分数分别为78.39%和62.71%;炉底灰渣中Ca和Fe的质量分数较炉顶飞灰高,而炉顶飞灰中Si和Al的质量分数则比炉底灰渣高;气化灰渣中的矿物质主要以对气化反应无催化活性的惰性物质形态存在,炉底灰渣中对含碳物料气化反应有催化作用的主要是少量的硫酸钙、氧化铁和钾芒硝(K3Na(SO4)2),而炉顶飞灰中则是少量的硫酸钙;随着气化灰渣添加量的增加,石油焦催化气化反应速率达到最大值时所对应的转化率逐渐减小。当气化灰渣的添加量为5%~30%时,石油焦的气化活性提高了2~7倍,其中炉底灰渣的催化活性稍优于炉顶飞灰。

  13. Catalytic hydrotreating process

    Science.gov (United States)

    Karr, Jr., Clarence; McCaskill, Kenneth B.

    1978-01-01

    Carbonaceous liquids boiling above about 300.degree. C such as tars, petroleum residuals, shale oils and coal-derived liquids are catalytically hydrotreated by introducing the carbonaceous liquid into a reaction zone at a temperature in the range of 300.degree. to 450.degree. C and a pressure in the range of 300 to 4000 psig for effecting contact between the carbonaceous liquid and a catalytic transition metal sulfide in the reaction zone as a layer on a hydrogen permeable transition metal substrate and then introducing hydrogen into the reaction zone by diffusing the hydrogen through the substrate to effect the hydrogenation of the carbonaceous liquid in the presence of the catalytic sulfide layer.

  14. Sustainable development with clean coal

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-08-01

    This paper discusses the opportunities available with clean coal technologies. Applications include new power plants, retrofitting and repowering of existing power plants, steelmaking, cement making, paper manufacturing, cogeneration facilities, and district heating plants. An appendix describes the clean coal technologies. These include coal preparation (physical cleaning, low-rank upgrading, bituminous coal preparation); combustion technologies (fluidized-bed combustion and NOx control); post-combustion cleaning (particulate control, sulfur dioxide control, nitrogen oxide control); and conversion with the integrated gasification combined cycle.

  15. Numerical simulation of catalytic methanation process of producing natural gas using coal%煤制天然气过程催化甲烷化的数值模拟

    Institute of Scientific and Technical Information of China (English)

    王翠苹; 李刚; 李厚洋; 姜旭

    2015-01-01

    两步法煤制天然气的第一步反应主要生产粗煤气CO和 H2,调整CO与 H2的比值后进行甲烷化反应。在计算软件HSC中分别控制反应温度、压力和CO与H2比例,计算了甲烷化产物变化规律,得到第二步甲烷化反应最适条件是1.8 M Pa、700℃;通过在计算软件FL U EN T 中进行一步对催化甲烷化反应的模拟,0.1 M Pa、720℃时的催化甲烷化即可达到无催化高压条件的甲烷摩尔产率,甲烷化产率最高时对应的n(H2)∶ n(C O )比值为1.8。%The main products from the first step reaction of the two‐step coal gasification are CO and H2 ,and the ratio of CO to H2 can be adjusted for the next methanation reaction step .A computing software HSC was used to compute the methanation product changing trend by controlling the reaction temperature , pressure and CO/H2 ratio , and the optimum condition for the second step reaction was derived as 1 .8 MPa and 700 ℃ .The catalytic methanation reaction was simulated using commercial software Fluent ,and the coal gasification and methanation reaction occurred successively in a one‐step reactor .The methanation productivity of catalytic methanation under the condition of 720 ℃ and 0 .1 MPa is comparable to the high pressure production without catalytic reaction .The CO/H2 ratio of is up to 1 .8 w hen the highest methanation yield is achieved .

  16. RESEARCH ON REUSE OF PAPERMAKING LIGNIN-CONVERSION OF LIGNIN TO BTX BY CATALYTIC PYROLYSIS IN A POWDER PARTICLE FLUIDIZED BED

    Institute of Scientific and Technical Information of China (English)

    Chang Wang; Chongwo Li; Qingzhu Jia

    2004-01-01

    Experiments on the catalytic pyrolysis of the papermaking lignin were conduced by using a new type of powder-particle fluidized bed to improve the yield of the light aromatic hydrocarbon, i.e. benzene,toluene, xylene and naphthalene (BTXN), in which the primary decomposition and secondary catalytic reaction occur simultaneously at ambient pressure.The effect of catalyst species, fluidizing gases and pyrolysis temperature on the yield of the BTXN were investigated. The content of sulfur is high in the papermaking lignin, and the volatile matter is effected by the temperature. In the case of the inert media silica sand, the yield and the distribution of the pyrolysis products were almost unchanged under the different kind of atmosphere. In the case of the catalyst CoMo-B with hydrogen atmosphere, the intermediate BTXN yield reached 2.52wt%, dry, 3.3 times as much as that in the case of silica sand.Therefore, in order to obtain valuable BTXN as an intermediate in the pyrolysis as much as possible, it is extremely important to select high sulfur resistance and hydrogenization activity catalyst.

  17. RESEARCH ON REUSE OF PAPERMAKING LIGNIN-CONVERSION OF LIGNIN TO BTX BY CATALYTIC PYROLYSIS IN A POWDER PARTICLE FLUIDIZED BED

    Institute of Scientific and Technical Information of China (English)

    ChangWang; ChongwoLi; QingzhuJia

    2004-01-01

    Experiments on the catalytic pyrolysis of the papermaking lignin were conduced by using a new type of powder-particle fluidized bed to improve the yield of the light aromatic hydrocarbon, i.e. benzene, toluene, xylene and naphthalene (BTXN), in which the primary decomposition and secondary catalytic reaction occur simultaneously at ambient pressure. The effect of catalyst species, fluidizing gases and pyrolysis temperature on the yield of the BTXN were investigated. The content of sulfur is high in the papermaking lignin, and the volatile matter is effected by the temperature. In the case of the inert media silica sand, the yield and the distribution of the pyrolysis products were almost unchanged under the different kind of atmosphere. In the case of the catalyst CoMo-B with hydrogen atmosphere, the intermediate BTXN yield reached 2.52wt%, dry, 3.3 times as much as that in the case of silica sand. Therefore, in order to obtain valuable BTXN as an intermediate in the pyrolysis as much as possible, it is extremely important to select high sulfur resistance and hydrogenization activity catalyst.

  18. Demonstration of selective catalytic reduction technology for the control of nitrogen oxide emissions from high-sulfur, coal-fired boilers

    Energy Technology Data Exchange (ETDEWEB)

    Hinton, W.S.; Powell, C.A.; Maxwell, J.D.

    1993-11-01

    This paper describes the status of the Innovative Clean Coal Technology project to demonstrate SCR technology for reduction of NO{sub x} emissions from flue gas of utility boilers burning US high-sulfur coal. The funding participants are the US Department of Energy (DOE), Southern Company Services, Inc. (SCS), on behalf of the entire Southern Company, Electric Power Research Institute (EPRI), and Ontario Hydro. SCS is the participant responsible for managing all aspects of the project. The project is being conducted on Gulf Power Company`s Plant Crist Unit 5 (75-MW nominal capacity), located near Pensacola, Florida, on US coals that have a sulfur content near 3.0%. The SCR facility treats a 17,400 scfm slip-stream of flue gas and consists of three 2.5-MW (5000 scfm) and six 0.2-MW (400 scfm) SCR reactors. The reactors operate in parallel with commercially available SCR catalysts obtained from vendors throughout the world. The design engineering and construction have been completed, and the startup/shakedown was completed in June 1993. Long-term performance testing began in July 1993 and will be conducted for two years. Test facility description and test plans, as well as start-up issues and preliminary commissioning test results are reported in this paper.

  19. Influence of Injection Angle of Oxygen on Velocity Field in Conversion Furnace of Coal-methanol%氧气喷射角度对煤制甲醇转化炉内速度场的影响

    Institute of Scientific and Technical Information of China (English)

    李曙阳; 伍永福

    2015-01-01

    In order to study the influence of injection angle of oxygen on velocity field in conversion furnace of coal-methanol, the mathematical model of conversion furnace of coal-methanol was built with ANSYS and Fluent. The pressure field of conversion furnace of coal-methanol was simulated as the injection angle was 0°,8°,11° or 15°.The results show that the minimum velocity gradient can appear as the injection angle is 0°,the high speed area is the smallest and the region extends along the axial direction, the combustion of coke oven gas is the stablest,the quenching of flame is not easy to happen.%为了研究氧气喷射角度对煤制甲醇转化炉中速度场的影响,利用 ANSYS 和 Fluent 软件构建煤制甲醇转化炉模型,研究了氧气喷射角度在0°、8°、11°和15°时对转化炉内速度分布变化,发现氧气喷射角度在0°时,转化炉内速度梯度最小,高速区域最小且沿轴向延展,火焰最稳定,不易出现火焰淬灭现象。

  20. Cellulosic Biomass Sugars to Advantage Jet Fuel: Catalytic Conversion of Corn Stover to Energy Dense, Low Freeze Point Paraffins and Naphthenes: Cooperative Research and Development Final Report, CRADA Number CRD-12-462

    Energy Technology Data Exchange (ETDEWEB)

    Elander, Rick [National Renewable Energy Lab. (NREL), Golden, CO (United States)

    2015-08-04

    NREL will provide scientific and engineering support to Virent Energy Systems in three technical areas: Process Development/Biomass Deconstruction; Catalyst Fundamentals; and Technoeconomic Analysis. The overarching objective of this project is to develop the first fully integrated process that can convert a lignocellulosic feedstock (e.g., corn stover) efficiently and cost effectively to a mix of hydrocarbons ideally suited for blending into jet fuel. The proposed project will investigate the integration of Virent Energy System’s novel aqueous phase reforming (APR) catalytic conversion technology (BioForming®) with deconstruction technologies being investigated by NREL at the 1-500L scale. Corn stover was chosen as a representative large volume, sustainable feedstock.

  1. Thermoelectric power plant conversion from fuel oil to coal with integration of a CO{sub 2} capture plant. Part 1; Conversion de una central termoelectrica de combustoleo a carbon con integracion de una planta de captura de CO{sub 2}. Parte 1

    Energy Technology Data Exchange (ETDEWEB)

    Huante Perez, Liborio; Rodriguez Martinez, J. Hugo; Arriola Medellin, Alejandro M. [Instituto de Investigaciones Electricas, Cuernavaca, Morelos (Mexico)

    2010-11-15

    The major features in the design of power plant conversion from fuel oil to coal, considering the new technical characteristics of fuel and his transportation to plant, equipment required to comply with Mexican environmental standards and additional requirements of auxiliaries are described. In addition, changes needed on power plant design were considered according to integrates CO{sub 2} capture plant alternatives. [Spanish] En este articulo se describen las caracteristicas principales en el diseno de la conversion de Centrales de combustoleo a carbon, considerando el nuevo combustible y su transporte hasta la central, los equipos requeridos para cumplir con las normas ambientales y los requerimientos adicionales de los servicios auxiliares. Adicionalmente, se lleva a cabo el analisis de los cambios requeridos en el diseno de la conversion considerando diferentes opciones para la integracion de una planta de captura de CO{sub 2}, la cual debera entregar este subproducto para su compresion y envio a su destino final para su almacenamiento.

  2. H{sub 3}PO{sub 4}/Al{sub 2}O{sub 3} catalysts: characterization and catalytic evaluation of oleic acid conversion to biofuels and biolubricant

    Energy Technology Data Exchange (ETDEWEB)

    Araujo, Lucia Regina Raddi de; Scofield, Cynthia Fraga [Universidade do Estado do Rio de Janeiro (UERJ), RJ (Brazil). Inst. de Quimica]. E-mail: luraddi@uerj.br. Pastura, Nidia Maria Ribeiro; Gonzalez, Wilma de Araujo [Instituto Militar de Engenharia (IME), Rio de Janeiro, RJ (Brazil). Dept. de Engenharia Quimica

    2006-04-15

    Al{sub 2}O{sub 3} and H{sub 3}PO{sub 4}/Al{sub 2}O{sub 3} catalysts were investigated in the conversion of oleic acid to bio fuels and bio lubricant at 1 atm and at 623 K. The catalytic tests were performed in a fixed bed and continuous flow reactor, using an oleic acid-catalyst ratio of 4 and N{sub 2} as the carrier gas. The reaction products were analyzed by gas chromatography and acidity measurements. N{sub 2} adsorption-desorption, X ray diffraction, {sup 31}P nuclear magnetic resonance and FT-IR spectroscopy were also employed to evaluate the textural, structural and acidic properties of the catalysts. The results showed that phosphoric acid impregnation improved the alumina decarboxylation activities, generating hydrocarbons in the range of gasoline, diesel oil and lubricant oil. The best catalytic performance was achieved with the highest surface area alumina impregnated with H{sub 3}PO{sub 4}, which was the solid that allied high total acidity with a large quantity of meso pores. (author)

  3. Advanced treatment of coal gasification wastewater by catalytic oxidation with trace ozone%微量臭氧催化氧化深度处理煤气化废水

    Institute of Scientific and Technical Information of China (English)

    张国涛; 万新华; 李伟; 杨延红; 王丽梅

    2013-01-01

    An experimental research on advanced treatment of underground coal gasification wastewater by catalytic ozonation was carried out, which happened continuously in a fixed bed reactor loaded with solid catalysts and effects of trace ozone as oxidants on catalytic ozonation were studied. The results showed that when wastewater COD was 300 mg/L or so, the treatment unit' s COD removal increased by 45% with trace ozone added in, with each mg ozone treating 2. 4 mg organic compounds on average. And it was also found that the optimum ozone dosage for wastewater with COD 200 mg/L was approximately 20 mg ozone per liter wastewater where wastewater inflow was 1 L/h and gas-water ratio was 15 : 1. Meanwhile, experiments showed that wastewater chroma was efficiently removed by catalytic ozonation. Compared with peers experimental research, the technology of catalytic oxidation with trace ozone in advanced wastewater treatment was cost-effective.%采取固定床连续式水处理方式,实验研究了在固体催化剂作用下微量臭氧催化氧化深度处理地下煤气化废水的效果.结果表明,当处理COD为300 mg,/L左右的该类型废水时,加入微量臭氧,水处理装置COD去除率提高了45%,平均1 mg的臭氧处理了2.4 mg有机物;当废水COD为200 mg/L左右,进水速度为1 L/h时,最佳臭氧投加量为每升废水20 mg左右的臭氧,此时气水比为15:1左右;同时实验发现,不同COD的废水色度均可以被有效去除.通过与其他类似的实验研究比较发现,微量臭氧催化氧化技术具有成本优势.

  4. Chemistry and structure of coal derived asphaltenes and preasphaltenes. Quarterly progress report, April-June 1980

    Energy Technology Data Exchange (ETDEWEB)

    Yen, T. F.

    1980-01-01

    It is the objective of this project to isolate the asphaltene and preasphaltene fractions from coal liquids from a number of liquefaction processes. These processes consist of in general: catalytic hydrogenation, staged pyrolysis and solvent refining. These asphaltene fractions may be further separated by both gradient elution through column chromatography, and molecular size distribution through gel permeation chromatography. Those coal-derived asphaltene and preasphaltene fractions will be investigated by various chemical and physical methods for characterization of their structures. After the parameters are obtained, these parameters will be correlated with the refining and conversion variables which control a given type of liquefaction process. The effects of asphaltene in catalysis, ash or metal removal, desulfurization and denitrification will also be correlated. It is anticipated that understanding the role of asphaltenes in liquefaction processes will enable engineers to both improve existing processes, and to make recommendations for operational changes in planned liquefaction units in the United States. The objective of Phase 1 was to complete the isolation and separation of coal liquid fractions and to initiate their characterization. The objective of Phase 2 is to continue the characterization of coal asphaltenes and other coal liquid fractions by use of physical and instrumental methods. The structural parameters obtained will be used to postulate hypothetical average structures for coal liquid fractions. The objective of Phase 3 is to concentrate on the characterization of the preasphaltene (benzene insoluble fraction) of coal liquid fraction by the available physical and chemical methods to obtain a number of structural parameters.

  5. Effects of Feed Composition and Feed Impurities in the Catalytic Conversion of Syngas to Higher Alcohols over Alkali-Promoted Cobalt–Molybdenum Sulfide

    DEFF Research Database (Denmark)

    Christensen, Jakob Munkholt; Jensen, Peter Arendt; Jensen, Anker Degn

    2011-01-01

    Alkali-promoted cobalt–molybdenum sulfide is a potential catalyst for the conversion of syngas into higher alcohols. This work is an investigation of how the feed composition influences the behavior of the sulfide catalyst. In a sulfur-free syngas the production of higher alcohols is observed...... to be optimal with an equimolar mixture of CO and H2 in the feed, while the methanol production benefits from an increasing hydrogen content in the feed. The influence of NH3 and H2O in the syngas feed has also been investigated. Ammonia (741 ppmv) in the feed is observed to cause a general and largely...

  6. CeO2-TiO2 catalysts for catalytic oxidation of elemental mercury in low-rank coal combustion flue gas.

    Science.gov (United States)

    Li, Hailong; Wu, Chang-Yu; Li, Ying; Zhang, Junying

    2011-09-01

    CeO(2)-TiO(2) (CeTi) catalysts synthesized by an ultrasound-assisted impregnation method were employed to oxidize elemental mercury (Hg(0)) in simulated low-rank (sub-bituminous and lignite) coal combustion flue gas. The CeTi catalysts with a CeO(2)/TiO(2) weight ratio of 1-2 exhibited high Hg(0) oxidation activity from 150 to 250 °C. The high concentrations of surface cerium and oxygen were responsible for their superior performance. Hg(0) oxidation over CeTi catalysts was proposed to follow the Langmuir-Hinshelwood mechanism whereby reactive species from adsorbed flue gas components react with adjacently adsorbed Hg(0). In the presence of O(2), a promotional effect of HCl, NO, and SO(2) on Hg(0) oxidation was observed. Without O(2), HCl and NO still promoted Hg(0) oxidation due to the surface oxygen, while SO(2) inhibited Hg(0) adsorption and subsequent oxidation. Water vapor also inhibited Hg(0) oxidation. HCl was the most effective flue gas component responsible for Hg(0) oxidation. However, the combination of SO(2) and NO without HCl also resulted in high Hg(0) oxidation efficiency. This superior oxidation capability is advantageous to Hg(0) oxidation in low-rank coal combustion flue gas with low HCl concentration.

  7. Influence of catalytic activity and reaction conditions on the product distribution in coal liquefaction; Sekitan ekikayu no seiseibutsu bunpu ni taisuru shokubai kassei oyobi hanno joken no eikyo

    Energy Technology Data Exchange (ETDEWEB)

    Hasuo, H.; Sakanishi, K.; Mochida, I. [Kyushu University, Fukuoka (Japan). Institute of Advanced Material Study

    1996-10-28

    The NiMo sulfide supported on Ketjen Black (KB) was more effective and yielded lighter oil products containing light fractions with their boiling point below 300{degree}C during the two stage liquefaction combining low temperature and high temperature hydrogenation the conventional NiMo/alumina catalyst and FeS2 catalyst. Although the NiMo/alumina yielded increased oil products during the two stage liquefaction, the lighter oil fractions did not increase and the heavier fractions increased mainly. This suggests that the hydrogenation of aromatic rings and successive cleavage of the rings are necessary for producing the light oil, which is derived from the sufficient hydrogenation of aromatic rings using catalysts. For the two stage reaction with NiMo/KB catalyst, it was considered that sufficient hydrogen was directly transferred to coal molecules at the first stage of the low temperature reaction, which promoted the solubilization of coal and the successive hydrogenation at the high temperature reaction. Thus, high activity of the catalyst must be obtained. It is expected that further high quality distillates can be produced through the optimization of catalysts and solvents at the two stage reaction. 1 ref., 4 figs., 1 tab.

  8. Effect of properties of iron compounds on the catalytic activity in direct coal liquefaction; Tetsu kagobutsu no keitai to sekitan ekika kassei

    Energy Technology Data Exchange (ETDEWEB)

    Kaneko, T.; Tazawa, K. [Mitsubishi Chemical Corp., Tokyo (Japan); Shimasaki, K. [Kobe Steel Ltd. (Japan)

    1998-08-20

    When considering merchandising scale of the coal liquefaction process, it is a preliminary condition that metal used for its catalyst is rich in resource volume, cheap in production cost, without pollution, and so forth, and application of cheap iron ore and ferrous compounds to disposable catalyst is desired. As liquefaction activity of the iron ore was hitherto improved by its micro crushing, its mechanical crush had a limit of about 2 {mu}m in mean particle diameter. However, together with recent crushing technique, crushers with high performance were developed, and then micro crushing by sub-micron became possible industri8ally even for iron ore. In this study, three kinds of Australian iron ores such as limonite of ferric hydroxide type iron ore, pyrite of ferrous sulfide type, and hematite of ferric oxide type were micro crushed to examine coal liquefaction activity and hydrogenation reaction activity of 1-methyl naphthalene (1-MN) and also relationship between properties and activity of catalyst for the latter before and after reaction. 11 refs., 8 figs., 5 tabs.

  9. Innovative Clean Coal Technology (ICCT). Demonstration of Selective Catalytic Reduction (SCR) technology for the control of nitrogen oxide (NO{sub x}) emissions from high-sulfur coal-fired boilers: Volume 2, Appendices A--N. Final report

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-10-01

    Volume 2 contains the following appendices: Appendix A, Example Material Safety Data Sheet; Appendix B, Initial Site Characterization Test Results; Appendix C, Testing Proposal, Southern Research Institute; Appendix D, Example Laboratory Catalyst Test Protocol; Appendix E, Detailed Coal Analysis Data; Appendix F, Standard Methods-QA/QC Document; Appendix G, Task No. 1 Commissioning Tests; Appendix H, Task No. 2 Commissioning Tests; Appendix I, First Parametric Sequence Spreadsheets; Appendix J, Second Parametric Sequence Spreadsheets; Appendix K, Third Parametric Sequence Spreadsheets; Appendix L, Fourth Parametric Sequence Spreadsheets; Appendix M, Fifth Parametric Sequence Spreadsheets; and Appendix N, First Series-Manual APH Tests.

  10. Catalytic Conversion of Bio-Oil to Oxygen-Containing Fuels by Acid-Catalyzed Reaction with Olefins and Alcohols over Silica Sulfuric Acid

    Directory of Open Access Journals (Sweden)

    Qingwen Wang

    2013-09-01

    Full Text Available Crude bio-oil from pine chip fast pyrolysis was upgraded with olefins (1-octene, cyclohexene, 1,7-octadiene, and 2,4,4-trimethylpentene plus 1-butanol (iso-butanol, t-butanol and ethanol at 120 °C using a silica sulfuric acid (SSA catalyst that possesses a good catalytic activity and stability. Gas chromatography-mass spectrometry (GC-MS, Fourier transform infrared spectroscopy (FT-IR and proton nuclear magnetic resonance (1H-NMR analysis showed that upgrading sharply increased ester content and decreased the amounts of levoglucosan, phenols, polyhydric alcohols and carboxylic acids. Upgrading lowered acidity (pH value rose from 2.5 to >3.5, removed the unpleasant odor and increased hydrocarbon solubility. Water content dramatically decreased from 37.2% to about 7.0% and the heating value increased from 12.6 MJ·kg−1 to about 31.9 MJ·kg−1. This work has proved that bio-oil upgrading with a primary olefin plus 1-butanol is a feasible route where all the original heating value of the bio-oil plus the added olefin and alcohol are present in the resulting fuel.

  11. Characteristics of American coals in relation to their conversion into clean energy fuels. Quarterly technical progress report, October--December 1977

    Energy Technology Data Exchange (ETDEWEB)

    Spackman, W.; Davis, A.; Walker, P. L.; Lovell, H. L.; Essenhigh, R. H.; Vastola, F. J.; Given, P. H.; Suhr, N. H.

    1978-03-01

    The Penn State/DOE Coal Sample Bank has been expanded. A total of 54 characterized coal samples and 232 selected printouts of coal data were provided upon request to the coal research community. Work has been conducted using nitrogen as a pyrolysis medium at 808/sup 0/C and seven size grades of the Texas Darco lignite (PSOC-412) as starting material. This work was intended to extend previous work on the effects of particle size on pyrolysis. A study is being made into the effects of low temperature oxidation on the agglomerating properties of caking coals. The effect of preoxidation in air of a highly caking coal at different temperatures on weight loss during pyrolysis up to 1000/sup 0/C and reactivity of resultant chars to air at 475/sup 0/C has been investigated. Preoxidation has essentially no effect on weight loss during pyrolysis below 450/sup 0/C. At higher temperatures, however, preoxidation results in a decrease in weight loss. Preoxidation markedly enhances subsequent char reactivity. Differential scanning calorimetry and thermogravimetric analysis have been used to study the interaction between oxygen and an unactivated Saran carbon. In the range 125-227/sup 0/C, chemisorption of oxygen, though the predominant process, is associated with a gasification reaction. The rate of the latter reaction is much higher than extrapolated from the Arrhenius plot in the temperature range 450-550/sup 0/C. In the temperature range 450-850/sup 0/C, gasification kinetics have been studied by the TGA technique. Plots of burn-off versus reaction time are linear over the 15-65% burn-off range. The Arrhenius plots consist of three distinct straight lines of different slopes, indicating that the gasification reaction occurs in three different zones.

  12. Contribution to Conversion of CO2 to fuel by electro-photo-catalytic reduction in hydro-genocarbonated aqueous solution tion

    Science.gov (United States)

    Nezzal, Ghania; Benammar, Souad; Hamouni, Samia; Meziane, Dalila; Naama, Sabrina; Abdessemed, Djamel

    2015-04-01

    Referring to the last World Conference COPENHAGEN (2010), endorsed by the United Nations,to '' RISKS OF CLIMATE CHANGES ', states had not reached an agreement to work fairly, in an international program, to limit Carbon dioxide emissions into the atmosphere, to put off it, to the next (in 2015), the right decisions, despite the recommendations of the 'IPCC'. Based on the natural reaction of photosynthesis, which converts carbon dioxide in the presence of water and sun, to '' OSA'' ', it is natural that scientists believe to implement an artificial conversion of CO2 in a renewable energy faster. Our contribution focuses on the same goals, by a different line. In this perspective, nano-materials, catalysts, pervaporation membranes, pervaporation unit, and a photo-reactor prototype, have been made. A summary of the preliminary results presented: For example, are given the concentrations of the various species present in a aqueous solution of sodium hydrogen carbonate, 0.5M, saturated with CO2, at standard temperature and pressure: (CO2) = 1M; (H2CO3) = 0,038M; (HCO3-) = 0,336M; (CO3 --) = 0,34M; pH = 7.33, an overall concentration = 1,714M, more than three times that of the initial solution. It is in such conditions that the conversion of carbon dioxide by the hydrogen produced in situ by electrolysis, in fuel, must be done in the presence of catalyst, under UV radiation. For electrodes, a nano-porous layer was formed on their surface to receive the suitable catalyst. These lats prepared, are made of porous supports (montmorillonite, aluminum and silicon oxides) into which are inserted the metal precursor, by impregnation interactive, in Iron, cobalt, nickel salt solutions, cobalt, nickel. Their performance has been identified by the reduction of para- nitrophenol, to para-aminophenol in aqueous medium in the presence of sodium borohydride. This is the catalyst 'Cobalt supported by SiO2'' that gave the best conversion, 99.5% instead of 99.7%, for a platinum catalyst

  13. Effect of burn-off on physical and chemical properties of coal char; Gas ka shinko ni tomonau sekitan char no tokusei henka

    Energy Technology Data Exchange (ETDEWEB)

    Yamada, T.; Tamura, K.; Hashimoto, H.; Funaki, M.; Suzuki, T. [Kitami Institute of Technology, Hokkaido (Japan)

    1996-10-28

    For high-efficiency coal gasification, investigations were given on effect of coal chars with different conversion rates on coal gasification reactivity. In coal gasification, reactivity of char after pyrolysis governs the efficiency. The reference char conversion in CO2 gasification of coal (weight loss) changes linearly in the initial stage of the reaction, but the reactivity declines as the end point is approached. Char surface area is as large as 400 m{sup 2}/g in the initial stage with the conversion at 20%, but it decreases in the final stage. This phenomenon relates closely with changes in pore size and crystalline structure. Change in the Raman value R which shows incompleteness of char graphite structure and amorphous carbon ratio suggests that an active portion with high reactivity is oxidized preferentially, and a portion with low reactivity remains finally. Minerals in coal are known to accelerate the gasification. However, their catalytic effect is related with chemical forms, and complex as they may change into inactive sulfides and silicates under severe reaction conditions. Change in forms of calcium compounds may also be involved in decline of the reactivity in the latter stage. 8 refs., 4 figs.

  14. Influences of Different Preparation Conditions on Catalytic Activity of Ag2O-Co3O4/γ-Al2O3 for Hydrogenation of Coal Pyrolysis

    Directory of Open Access Journals (Sweden)

    Lei Zhang

    2014-01-01

    Full Text Available A series of catalysts of Ag2O-Co3O4/γ-Al2O3 was prepared by equivalent volume impregnation method. The effects of the metal loading, calcination time, and calcination temperatures of Ag and Co, respectively, on the catalytic activity were investigated. The optimum preparing condition of Ag2O-Co3O4/γ-Al2O3 was decided, and then the influence of different preparation conditions on catalytic activity of Ag2O-Co3O4/γ-Al2O3 was analyzed. The results showed the following: (1 at the same preparation condition, when silver loading was 8%, the Ag2O-Co3O4/γ-Al2O3 showed higher catalyst activity, (2 the catalyst activity had obviously improved when the cobalt loading was 8%, while it was weaker at loadings 5% and 10%, (3 the catalyst activity was influenced by different calcination temperatures of silver, but the influences were not marked, (4 the catalyst activity can be influenced by calcination time of silver, (5 different calcination times of cobalt can also influence the catalyst activity of Ag2O-Co3O4/γ-Al2O3, and (6 the best preparation conditions of the Ag2O-Co3O4/γ-Al2O3 were silver loading of 8%, calcination temperature of silver of 450°C, and calcinations time of silver of 4 h, while at the same time the cobalt loading was 8%, the calcination temperature of cobalt was 450°C, and calcination time of cobalt was 4 h.

  15. Catalytic pyrolysis of Huang Tu Miao coal: TG-FTIR study%应用TG-FTIR技术研究黄土庙煤催化热解特性

    Institute of Scientific and Technical Information of China (English)

    李爽; 陈静升; 冯秀燕; 杨斌; 马晓迅

    2013-01-01

    用浸渍法制备过渡金属氧化物担载型催化剂MOx/USY(M=Co、Mo、Co-Mo),用热重红外联用技术考察了MOx/USY催化剂对黄土庙(HTM)煤热解失重特性和热解产物生成规律的影响.热重实验结果表明,MOx/USY催化剂可使HTM煤热解的二次脱气条件更为温和,热解峰温分别提前14、23和9℃.动力学分析结果表明,MOx/USY催化剂可降低HTM煤样热解的活化能.FT-IR研究表明,MOx/USY催化剂可有效改善HTM煤热解产物的组成和分布,CoOx/USY催化剂能显著提高HTM煤热解产物中高热值气体(CO、CH4)和轻质芳烃以及脂肪烃类化合物的含量;MoOx/USY催化剂没有明显改善HTM煤热解产物组成和分布;MoOx-CoOx/USY催化剂可促进CO、CH4、轻质芳烃和脂肪烃类化合物的生成,却使热解产物的生成向高温区移动,说明USY负载的不同过渡金属氧化物对煤样热解行为和热解产物有较大影响.%MOx/USY catalysts ( M = Co, Mo, Co-Mo) were prepared by incipient wetness impregnation method. Catalytic pyrolysis of Huang Tu Miao (HTM) coal was investigated and the pyrolysis products were examined by TG-FTIR technique. TG results indicate that MOx/USY catalysts are effective in lowering degasifiction temperature (14, 23 and 9℃ respectively) in HTM coal pyrolysis. Kinetic calculations show that MOx/USY catalysts are effective in lowing activation energy of pyrolysis. FT-IR analyses show that the MOX/ USY catalysts are effective in manipulating coal pyrolysis products. CoOx/USY catalyst promote the generation of CH4, CO and aromatic hydrocarbons and aliphatic hydrocarbons in HTM coal pyrolysis. MoOx/USY catalyst show little effect in manipulating pyrolysis products. CoOx-MoOx/USY catalyst is a promising catalyst in giving high yield of volatile products, however the pyrolysis temperature moved to high temperature region. These results indicate that different metal oxides incorporated zeolite USY have different impact on manipulating

  16. 神府煤和锡林浩特煤的非均相光催化氧化%Photo-catalytic oxidation of Shenfu coal and Xilinhot lignite in heterogeneous hydration system

    Institute of Scientific and Technical Information of China (English)

    解恒参; 宗志敏; 刘彤; 魏晴; 赵建军; 赵培芝; 魏贤勇

    2011-01-01

    采用悬浮式非均相体系分别对水合神府烟煤(SFC)及锡林浩特褐煤(XL)进行选择性光催化氧化、傅里叶红外光谱(FTIR)分析及气相色谱质谱联用(GS/MS)检测,获得了反应产物的分子结构信息.同时对不同条件下煤炭降解效果的研究发现:芳香度和芳环取代度较高的烟煤组分光氧化性较弱,氧化后的产物中有较多酮类生成,而芳环取代度小、含有较多亚甲基和脂肪族侧链的褐煤光氧化性能较强,生成物中烯烃的含量明显减少;催化剂二氧化钛对光催化反应的影响要大于氧化剂过氧化氢,但在仅有过氧化氢存在情况下,随着其加入量的增大光氧化效果会更显著,煤样的投加量对光催化的影响不占主导地位;光催化氧化中,煤大分子中的烷基侧链易断裂脱除,特别是甲基和亚甲基易发生光催化氧化分解,而且碳氧单键的红外吸收峰强度明显减弱,表明煤大分子的侧链和碳氧单键在紫外光辐射环境下反应活性高.%Shenfu bituminous coal (SFC) and Xilinhot lignite (XL) were oxidized selectively using hydrogen peroxide in heterogeneous hydration suspension system and analyzed with FTIR and GC/MS technologies, meanwhile the oxidation effect of different conditions were also discussed. The results indicate that the photo-catalytic oxidation activity of the bituminous coal with high aromaticity correlation and alkyl substitutions on aromatic fractions is lower than that of Xilinhot lignite with lower alkyl substitutions on aromatic fractions and large of mehtyl and methylene. In the products a number of organic ketones are enough besides biphenyls in SFC, but the relative content of the alkenes is reduced obviously in XL. And the effect factors are in the order amount of photocatalyst>dosage of H2 O2 >amount of coal. However with the increasing of H202 dosage the oxidation of coals is much more significant. In the experiment the organic maters with branched

  17. Development of a self-consistent thermodynamic- and transport-property correlation framework for the coal conversion industry. Phase I. Semiannual report, September 1, 1980-February 28, 1981

    Energy Technology Data Exchange (ETDEWEB)

    Starling, K.E.; Lee, L.L.; Kumar, K.H.

    1981-01-01

    During the first half year of this research program the following elements of research have been performed: (1) the development of an improved pure component data bank, including collection and processing of data which is 70% complete as to substance, (2) calculation of distillable coal fluid thermodynamic properties using a multiparameter corresponding states correlation, (3) application of the most general density-cubic equation of pure fluids and (4) initiation of research to extend the corresponding states correlation framework to polar fluids. Primary conclusions of the first phase of this research program are that the three parameter corresponding states correlation predicts lighter coal fluid properties to a reasonable level of accuracy, and that a cubic equation can predict pure fluid thermodynamic properties on par with non-cubic equations of state.

  18. 二甲醚催化转化制甲苯的反应研究%Catalytic conversion of dimethyl ether to toluene over the molecular sieves modified with tungsten oxide

    Institute of Scientific and Technical Information of China (English)

    王博; 王辉; 刘广波; 李琢; 李学民; 吴晋沪

    2014-01-01

    在氧气气氛中,对氧化钨改性的不同分子筛催化剂上二甲醚( DME)转化反应进行了评价。结果表明,WO3/HZSM-5催化剂上DME可以高选择性转化为甲苯,对其反应工艺条件进行了优化,常压、290℃、DME/O2比为2:1时,二甲醚几乎完全转化,转化率为98.97%,甲苯的选择性达到39.71%。对催化剂结构和酸性进行表征,结果表明,ZSM-5分子筛的孔道结构最有利于甲苯的生成,WO3的介入调整了HZSM-5分子筛表面的酸性活性位点分布,在氧气气氛中有效地抑制了副产物的生成,使产物中甲苯的选择性提高。%The catalytic performance of various zeolites modified with tungsten oxide in the conversion of dimethyl ether ( DME ) to toluene in the presence of oxygen was investigated in a continuous flow fixed-bed reactor. The results indicated that WO3/HZSM-5 as a catalyst is highly selective in the conversion of DME to toluene;under the optimized conditions, i. e. atmospheric pressure, 290℃, and with a DME/O2 mol ratio of 2:1, the conversion of DME is 98. 97%, with the selectivity of 39. 71% to toluene. The characterization results about the catalyst structure and acidity illustrate that the porous structure of ZSM-5 is suitable for the formation of toluene from DME. The doping of WO3 adjusts the distribution of the surface acid sites and then inhibits the formation of side-products in the presence of oxygen, which is able to enhance the selectivity to toluene.

  19. Advanced bioreactor systems for gaseous substrates: Conversion of synthesis gas to liquid fuels and removal of SO{sub X} and NO{sub X} from coal combustion gases

    Energy Technology Data Exchange (ETDEWEB)

    Selvaraj, P.T.; Kaufman, E.N.

    1996-06-01

    The purpose of this research program is the development and demonstration of a new generation of gaseous substrate based bioreactors for the production of liquid fuels from coal synthesis gas and the removal of NO{sub x} and SO{sub x} species from combustion flue gas. This R&D program is a joint effort between the staff of the Bioprocessing Research and Development Center (BRDC) of ORNL and the staff of Bioengineering Resources, Inc. (BRI) under a Cooperative Research and Development Agreement (CRADA). The Federal Coordinating Council for Science, Engineering, and Technology report entitled {open_quotes}Biotechnology for the 21st Century{close_quotes} and the recent Energy Policy Act of 1992 emphasizes research, development, and demonstration of the conversion of coal to gaseous and liquid fuels and the control of sulfur and nitrogen oxides in effluent streams. This R&D program presents an innovative approach to the use of bioprocessing concepts that will have utility in both of these identified areas.

  20. NITRIC OXIDE FORMATION DURING PULVERIZED COAL COMBUSTION

    Science.gov (United States)

    Data on the overall conversion of coal-nitrogen to NOx were obtained at 1250 K and 1750 K for a residence time of one second. The conversion of coal-nitrogen to NOx decreased monotonically with increasing fuel/oxygen equivalence ratio and decreased slightly with increasing temper...

  1. STUDY OF SOLVENT AND CATALYST INTERACTIONS IN DIRECT COAL LIQUEFACTION

    Energy Technology Data Exchange (ETDEWEB)

    Michael T. Klein

    2000-01-01

    There are several aspects of the Direct Coal Liquefaction process which are not fully understood and which if better understood might lead to improved yields and conversions. Among these questions are the roles of the catalyst and the solvent. While the solvent is known to act by transfer of hydrogen atoms to the free radicals formed by thermal breakdown of the coal in an uncatalyzed system, in the presence of a solid catalyst as is now currently practiced, the yields and conversions are higher than in an uncatalyzed system. The role of the catalyst in this case is not completely understood. DOE has funded many projects to produce ultrafine and more active catalysts in the expectation that better contact between catalyst and coal might result. This approach has met with limited success probably because mass transfer between two solids in a fluid medium i.e. the catalyst and the coal, is very poor. It is to develop an understanding of the role of the catalyst and solvent in Direct Liquefaction that this project was initiated. Specifically it was of interest to know whether direct contact between the coal and the catalyst was important. By separating the solid catalyst in a stainless steel basket permeable to the solvent but not the coal in the liquefaction reactor, it was shown that the catalyst still maintains a catalytic effect on the liquefaction process. There is apparently transfer of hydrogen atoms from the catalyst through the basket wall to the coal via the solvent. Strong hydrogen donor solvents appear to be more effective in this respect than weak hydrogen donors. It therefore appears that intimate contact between catalyst and coal is not a requirement, and that the role of the catalyst may be to restore the hydrogen donor strength to the solvent as the reaction proceeds. A range of solvents of varying hydrogen donor strength was investigated. Because of the extensive use of thermogravimetric analysis in this laboratory in was noted that the peak

  2. Formation of N2 in the fixed-bed pyrolysis of low rank coals and the mechanisms; Koteisho netsubunkai ni okeru teitankatan kara no N2 no sisei

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Z.; Otsuka, Y. [Tohoku University, Sendai (Japan). Institute for Chemical Reaction Science

    1996-10-28

    In order to establish coal NOx preventive measures, discussions were given on formation of N2 in the fixed-bed pyrolysis of low rank coals and the mechanisms thereof. Chinese ZN coal and German RB coal were used for the discussions. Both coals do not produce N2 at 600{degree}C, and the main product is volatile nitrogen. Conversion into N2 does not depend on heating rates, but increases linearly with increasing temperature, and reaches 65% to 70% at 1200{degree}C. In contrast, char nitrogen decreases linearly with the temperature. More specifically, these phenomena suggest that the char nitrogen or its precursor is the major supply source of N2. When mineral substances are removed by using hydrochloric acid, their catalytic action is lost, and conversion into N2 decreases remarkably. Iron existing in ion-exchanged condition in low-rank coal is reduced and finely diffused into metallic iron particles. The particles react with heterocyclic nitrogen compounds and turn into iron nitride. A solid phase reaction mechanism may be conceived, in which N2 is produced due to decomposition of the iron nitride. 5 refs., 4 figs., 1 tab.

  3. Surfactant-Assisted Coal Liquefaction

    Science.gov (United States)

    Hickey, Gregory S.; Sharma, Pramod K.

    1993-01-01

    Obtaining liquid fuels from coal which are economically competitive with those obtained from petroleum based sources is a significant challenge for the researcher as well as the chemical industry. Presently, the economics of coal liquefaction are not favorable because of relatively intense processing conditions (temperatures of 430 degrees C and pressures of 2200 psig), use of a costly catalyst, and a low quality product slate of relatively high boiling fractions. The economics could be made more favorable by achieving adequate coal conversions at less intense processing conditions and improving the product slate. A study has been carried out to examine the effect of a surfactant in reducing particle agglomeration and improving hydrodynamics in the coal liquefaction reactor to increase coal conversions...

  4. Direct Catalytic Conversion of Cellobiose into Sorbitol in Extremely Low Acid over Ruthenium Catalysts%超低酸性环境中Ru/C催化纤维二糖一步法制备山梨醇的研究

    Institute of Scientific and Technical Information of China (English)

    李计彪; 武书彬; 张军

    2012-01-01

    以Ru/C为催化剂,在超低酸环境和氢气气氛下,将纤维二糖一步转化制备山梨醇.考察了反应温度、反应时间以及催化剂用量对山梨醇产率的影响.实验结果表明,在0.05%H3PO4环境,Ru/C催化剂用量15%,转速为600 r/min,反应温度为458 K以及3 MPa氢气条件下反应1h,产物山梨醇的产率最高,可达到87.1%.同时,催化剂重复利用研究表明Ru/C是一种较理想的氢化反应催化剂,可重复利用且催化效率较高.%Ru/C catalyst and extremely low acid were employed for one-step conversion of cellobiose into sorbitol in the presence of hydrogen. Effects of reaction temperature, reaction time and catalyst usage on sorbitol yield were discussed. Experimental results showed that the highest sorbitol yield of 87. 1% was obtained at reaction temperature of 458 K and catalyst usage of 15 % for 1 h under 3 MPa H2 with the stirring rate of 600 r/min. Meanwhile, catalyst recycling showed that Ru/C was an ideal hydro-genation catalyst with high catalytic efficiency, which could be recycled several times.

  5. Coal gasification: New challenge for the Beaumont rotary feeder

    Science.gov (United States)

    Stelian, J.

    1977-01-01

    The use of rotary feeders in the coal gasification process is described with emphasis on the efficient conversion of coal to clean gaseous fuels. Commercial applications of the rotary feeder system are summarized.

  6. Catalytic nanoarchitectonics for environmentally compatible energy generation

    Directory of Open Access Journals (Sweden)

    Hideki Abe

    2016-01-01

    Full Text Available Environmentally compatible energy management is one of the biggest challenges of the 21st century. Low-temperature conversion of chemical to electrical energy is of particular importance to minimize the impact to the environment while sustaining the consumptive economy. In this review, we shed light on one of the most versatile energy-conversion technologies: heterogeneous catalysts. We establish the integrity of structural tailoring in heterogeneous catalysts at different scales in the context of an emerging paradigm in materials science: catalytic nanoarchitectonics. Fundamental backgrounds of energy-conversion catalysis are first provided together with a perspective through state-of-the-art energy-conversion catalysis including catalytic exhaust remediation, fuel-cell electrocatalysis and photosynthesis of solar fuels. Finally, the future evolution of catalytic nanoarchitectonics is overviewed: possible combinations of heterogeneous catalysts, organic molecules and even enzymes to realize reaction-selective, highly efficient and long-life energy conversion technologies which will meet the challenge we face.

  7. Effects of pretreatment and reduction on the Co/Al2O3 catalyst for CO hydrogenation

    Institute of Scientific and Technical Information of China (English)

    Xiaoping Dai; Changchun Yu

    2008-01-01

    The purpose of this study was to investigate the effect of preadsorbed CO at different temperatures,calcination temperatures,the combined influence of reduction temperature and time,and pretreatment using hydrogen or syngas as reduction agents on the F-T synthesis(FTS)activity and selectivity of Co/Al2O3 catalyst.The reactivity of the carbon species at higher preadsorption temperature with H2 in TPSR decreased,whereas the carbon-containing species showed higher reactivity over Co/Al2O3 catalyst with 10W calcination temperature.This agreed well with the order of catalytic activity for F-T synthesis on this catalyst.The catalytic activity of the catalyst varied with reduction temperature and time remarkably.CODEX optimization gave an optimum reduction temperature of 756 K and reduction time of 6.2 h and estimated C5+ yield perfectly.The pretreatment of Co/Al2O3 catalyst with different reduction agents (hydrogen or syngas)showed important influences on the catalytic performance.A high CO conversion and C5+yield were obtained on the catalyst reduced by hydrogen,wherea smethane selectivity on the catalyst reduced by syngas was much higher than that on the catalyst reduced by hydrogen.

  8. Energy Conversion Alternatives Study (ECAS), General Electric Phase 1. Volume 3: Energy conversion subsystems and components. Part 3: Gasification, process fuels, and balance of plant

    Science.gov (United States)

    Boothe, W. A.; Corman, J. C.; Johnson, G. G.; Cassel, T. A. V.

    1976-01-01

    Results are presented of an investigation of gasification and clean fuels from coal. Factors discussed include: coal and coal transportation costs; clean liquid and gas fuel process efficiencies and costs; and cost, performance, and environmental intrusion elements of the integrated low-Btu coal gasification system. Cost estimates for the balance-of-plant requirements associated with advanced energy conversion systems utilizing coal or coal-derived fuels are included.

  9. Advances in catalytic conversion of biomass carbohydrates into 2,5-furandicarboxylic acid%生物质碳水化合物催化转化制2,5-呋喃二甲酸的研究进展

    Institute of Scientific and Technical Information of China (English)

    刘贤响; 徐琼; 苏胜培; 尹笃林

    2016-01-01

    2,5-Furandicarboxylic acid(FDCA),an important biomass-based platform compound, may be used as an alternative of petrochemical resources for the synthesis of biodegradable polymers and other additives. Its applications were introduced and the recent advances in the catalytic conversion of biomass carbohydrates to FDCA,including conventional synthetic methods,catalytic oxidation of 5-hydroxymethylfurfural and other methods using biomass sugars as starting materials, were summarized in this paper. An efficient catalytic system for the direct conversion of biomass carbohydrates to FDCA is an important basis for technological breakthroughs in the field. Some suggestions were proposed for further research and development of the catalytic conversion of biomass carbohydrates to FDCA.%2,5-呋喃二甲酸(FDCA)是有望替代石化资源合成可降解高分子及助剂材料等的重要生物质基平台化合物。介绍了FDCA的用途,综述了以生物质碳水化合物为原料制备FDCA的方法,包括传统的合成方法、5-羟甲基糠醛催化氧化法以及以生物质糖类为原料制备的方法。开发高效催化反应体系是该领域亟待突破的重要瓶颈。对进一步开发从生物质碳水化合物催化转化成FDCA提出了一些建议和展望,为生物质催化精细转化领域创新提供参考。

  10. Research Progress of Technologies for Tar Production during Coal Pyrolysis%煤热解制焦油的工艺研究进展

    Institute of Scientific and Technical Information of China (English)

    贺新福; 杨蕾; 吴红菊; 周安宁

    2014-01-01

    Coal pyrolysis was an important technique for coal conversion.Coal tar , one of the products , was an important raw material for liquid fuels and chemicals.The technologies including pretreatment of coal , change of atmosphere , catalytic pyrolysis and catalytic hydropyrolysis , co -pyrolysis with other material and novel integrated pyrolysis technology were stated that can improve tar yield during coal pyrolysis process , the factors that effected tar yield and the mechanisms were discussed , as well as the advantages and disadvantages of each processes.%煤热解是一种重要的煤炭分质利用技术,中低温热解焦油是制取液体燃料和化学品的重要原料。本文从对煤进行预处理、改变热解气氛、催化热解与催化加氢热解、煤与其它物质共热解、新型耦合热解工艺等方面综述了煤热解制焦油的工艺研究进展,探讨了影响煤热解过程焦油产率的因素及机理,并对各工艺进行了评价。

  11. 煤矿乏风低浓度甲烷催化氧化数值模拟%NUMERICAL SIMULATION OF CATALYTIC OXIDATION OF COAL MINE VENTILATION AIR LOW CONCENTRIATION METHANE

    Institute of Scientific and Technical Information of China (English)

    王鹏飞; 冯涛; 陈丽娟; 郝小礼

    2012-01-01

    应用计算流体力学软件FLUENT,通过导入CHEMKIN格式详细化学反应机理对煤矿乏风低浓度甲烷气体在壁面涂有Pt催化剂的蜂窝陶瓷通道表面的催化氧化过程进行数值研究,计算分析了有、无催化剂情况下乏风低浓度甲烷在通道内的反应情况,同时进一步分析了乏风甲烷浓度、入口进气速度、通道壁面温度及通道直径对甲烷氧化率的影响。结果表明:在蜂窝陶瓷通道内壁负载Pt金属催化剂不仅可以降低乏风中低浓度甲烷氧化所需的温度,而且可以大大提高甲烷的氧化率;甲烷氧化率随着乏风甲烷浓度和通道壁面温度的升高而增大,随着入口进气速度和通道直径的增大而下降。%With importing the detailed methane/air chemical reaction mechanism, the computational fluid dynamics software FLUENT was applied to numerically simulate the catalytic oxidation of coal mine ventilation air methane in microchannel of honeycomb ceramic which was coated with catalyst Pt. It was analyzed the reaction of vetilation air low concentration methane in microchannel with and without catalyst Pt, and it was further analyzed the effect of methane concentration, gas speed, wall temperature and the diameter of microchannel on the methane oxidation rate. The results show that: 1 ) with catalyst Pt coated on microchannel,it not only drops the temperature of methane oxidation,and also improves the methane oxidation rate ; 2 ) the methane oxidation rate increases with the increase of methane concentration and wall temperature ; 3 ) the methane oxidation rate decreases with the increase of gas speed and the diameter of microchannel.

  12. Significance of RuO2 modified SCR catalyst for elemental mercury oxidation in coal-fired flue gas.

    Science.gov (United States)

    Yan, Naiqiang; Chen, Wanmiao; Chen, Jie; Qu, Zan; Guo, Yongfu; Yang, Shijian; Jia, Jinping

    2011-07-01

    Catalytic conversion of elemental mercury (Hg(0)) to its oxidized form has been considered as an effective way to enhance mercury removal from coal-fired power plants. In order to make good use of the existing selective catalytic reduction of NO(x) (SCR) catalysts as a cobenefit of Hg(0) conversion at lower level HCl in flue gas, various catalysts supported on titanium dioxide (TiO(2)) and commercial SCR catalysts were investigated at various cases. Among the tested catalysts, ruthenium oxides (RuO(2)) not only showed rather high catalytic activity on Hg(0) oxidation by itself, but also appeared to be well cooperative with the commercial SCR catalyst for Hg(0) conversion. In addition, the modified SCR catalyst with RuO(2) displayed an excellent tolerance to SO(2) and ammonia without any distinct negative effects on NO(x) reduction and SO(2) conversion. The demanded HCl concentration for Hg(0) oxidation can be reduced dramatically, and Hg(0) oxidation efficiency over RuO(2) doped SCR catalyst was over 90% even at about 5 ppm HCl in the simulated gases. Ru modified SCR catalyst shows a promising prospect for the cobenefit of mercury emission control.

  13. Novel bimetallic dispersed catalysts for temperature-programmed coal liquefaction

    Energy Technology Data Exchange (ETDEWEB)

    Chunshan, Song; Kirby, S.; Schmidt, E. [Pennsylvania State Univ., University Park, PA (United States)] [and others

    1995-12-31

    The objective of this project is to explore bimetallic dispersed catalysts for more efficient coal liquefaction. Coal liquefaction involves cleavage of methylene, dimethylene and ether bridges connecting various aromatic units and the reactions of various oxygen functional groups. This paper describes recent results on (1) hydrodeoxygenation of O-containing polycyclic model compounds using novel organometallic catalyst precursors; and (2) activity and selectivity of dispersed Fe catalysts from organometallic and inorganic precursors for hydrocracking of 4-(1-naphthylmethyl) bibenzyl. The results showed that some iron containing catalysts have higher activity in the sulfur-free form, contrary to conventional wisdom. Adding sulfur to Fe precursors with Cp-ligands decreased the activity of the resulting catalyst. This is in distinct contrast to the cases with iron pentacarbonyl and superfine Fe{sub 2}O{sub 3}, where S addition increased their catalytic activity substantially. A positive correlation between sulfur addition and increased activity can be seen, but a reversed trend between Fe cluster size and hydrocracking conversion could be observed, for carbonyl-type Fe precursors. It is apparent that the activity and selectivity of Fe catalysts for NMBB conversion depends strongly on both the type of ligand environment, the oxidation state and the number of intermetal bonds in the molecular precursor.

  14. PLASMA PYROLYSIS OF BROWN COAL

    OpenAIRE

    Plotczyk, W.; Resztak, A.; A.; Szymanski

    1990-01-01

    The specific energy of the substrate is defined as the ratio of the plasma jet energy to the mass of the coal. The influence of the specific energy of the brown coal (10 - 35 MJ/kg) on the yield and selectivity of the gaseous products formation was determined. The pyrolysis was performed in d.c. arc hydrogen plasma jet with the 25 kW power delivered to it. The higher specific energies of coal correlated to the higher conversion degrees of the substrates to C2H2 and CO as well as to the higher...

  15. The economic production of alcohol fuels from coal-derived synthesis gas

    Energy Technology Data Exchange (ETDEWEB)

    Kugler, E.L.; Dadyburjor, D.B.; Yang, R.Y.K. [West Virginia Univ., Morgantown, WV (United States)] [and others

    1995-12-31

    The objectives of this project are to discover, (1) study and evaluate novel heterogeneous catalytic systems for the production of oxygenated fuel enhancers from synthesis gas. Specifically, alternative methods of preparing catalysts are to be investigated, and novel catalysts, including sulfur-tolerant ones, are to be pursued. (Task 1); (2) explore, analytically and on the bench scale, novel reactor and process concepts for use in converting syngas to liquid fuel products. (Task 1); (3) simulate by computer the most energy efficient and economically efficient process for converting coal to energy, with primary focus on converting syngas to fuel alcohols. (Task 2); (4) develop on the bench scale the best holistic combination of chemistry, catalyst, reactor and total process configuration integrated with the overall coal conversion process to achieve economic optimization for the conversion of syngas to liquid products within the framework of achieving the maximum cost effective transformation of coal to energy equivalents. (Tasks 1 and 2); and (5) evaluate the combustion, emission and performance characteristics of fuel alcohols and blends of alcohols with petroleum-based fuels. (Task 2)

  16. Application of the SELECS methodology to evaluate socioeconomic and environmental impacts of commercial-scale coal liquefaction plants at six potential sites in Kentucky. Final report from the study on development of environmental guidelines for the selection of sites for fossil energy conversion facilities

    Energy Technology Data Exchange (ETDEWEB)

    Northrop, G. M.; D' Ambra, C. A.

    1980-11-01

    Environmental and socioeconomic impacts likely to occur during the operational phase of two coal liquefaction processes have been evaluated with SELECS (Site Evaluation for Energy Conversion Systems) for each of six potential sites in Kentucky for commercial scale facilities capable of processing about 26,000 tons of coal per stream day. The processes considered in this evaluation are SRC-I, a direct liquefaction route with solid boiler fuel as the principal product, and Coal-to-Methanol-to-Gasoline, an indirect liquefaction route with transportation fuel as the primary product. For comparative purposes, the impacts of a 2-gigawatt coal-fired steam-electric power plant (with coal requirements comparable to the liquefaction facilities) and an automobile parts manufacturing plant (with employment requirements of 849, comparable to the liquefaction facilities) have also been evaluated at each site. At each site, impacts have been evaluated for one or two nearby cities or towns and four to six counties where significant impacts might be expected. The SELECS methodology affords a well-organized and efficient approach to collecting and assessing a large volume of data needed to comprehensively determine the potential socioeconomic and environmental impacts resulting from the implementation of commercial scale synfuel and other energy conversion facilities. This study has also shown that SELECS is equally applicable to determine the impacts of other facilities, such as automobile parts manufacturing. In brief, the SELECS methodology serves the purpose of objectively screening sites in order to choose one at which adverse impacts will be least, and/or to determine what aspect of a proposed facility might be modified to lessen impacts at a specific site.

  17. Catalytic production of biodiesel

    Energy Technology Data Exchange (ETDEWEB)

    Theilgaard Madsen, A.

    2011-07-01

    The focus of this thesis is the catalytic production of diesel from biomass, especially emphasising catalytic conversion of waste vegetable oils and fats. In chapter 1 an introduction to biofuels and a review on different catalytic methods for diesel production from biomass is given. Two of these methods have been used industrially for a number of years already, namely the transesterification (and esterification) of oils and fats with methanol to form fatty acid methyl esters (FAME), and the hydrodeoxygenation (HDO) of fats and oils to form straight-chain alkanes. Other possible routes to diesel include upgrading and deoxygenation of pyrolysis oils or aqueous sludge wastes, condensations and reductions of sugars in aqueous phase (aqueous-phase reforming, APR) for monofunctional hydrocarbons, and gasification of any type of biomass followed by Fischer-Tropsch-synthesis for alkane biofuels. These methods have not yet been industrialised, but may be more promising due to the larger abundance of their potential feedstocks, especially waste feedstocks. Chapter 2 deals with formation of FAME from waste fats and oils. A range of acidic catalysts were tested in a model fat mixture of methanol, lauric acid and trioctanoin. Sulphonic acid-functionalised ionic liquids showed extremely fast convertion of lauric acid to methyl laurate, and trioctanoate was converted to methyl octanoate within 24 h. A catalyst based on a sulphonated carbon-matrix made by pyrolysing (or carbonising) carbohydrates, so-called sulphonated pyrolysed sucrose (SPS), was optimised further. No systematic dependency on pyrolysis and sulphonation conditions could be obtained, however, with respect to esterification activity, but high activity was obtained in the model fat mixture. SPS impregnated on opel-cell Al{sub 2}O{sub 3} and microporous SiO{sub 2} (ISPS) was much less active in the esterification than the original SPS powder due to low loading and thereby low number of strongly acidic sites on the

  18. 温室气体CO2资源化催化转化研究进展%Current status on catalytic conversion of greenhouse gas CO2 to value-added chemicals

    Institute of Scientific and Technical Information of China (English)

    杨烽; 王睿

    2013-01-01

    With the global low carbon economy era commences,the reduction and utilization of greenhouse gas becomes a major concern in the world.The reclamation of greenhouse gas CO2 and the new opportunity it brings in the research area of carbon chemistry will become a new hot spot in the research frontier of green catalysis.In this paper,various typical catalytic reaction pathways for enabling direct conversion of CO2 to useful value-added chemicals were reviewed,including oxidation of saturated hydrocarbon by CO2,synthesis of organic acids and esters with CO2.Furthermore,some comments were made regarding the advantages and disadvantages of the catalysts involved,and their underlying reaction mechanisms of CO2 activation by catalysis.Based on these discussions,future work in this category was proposed.The authors believes that,the task-oriented activation of CO2 is the key factor governing the whole process of its chemical utilization,where suitable catalysts with high activity need to be developed;the exploitation of new reaction media and use of new phase state CO2 may greatly enhance the conversion and selectivity of the reaction and hence deserve further investigation ;as to the direct use of CO2 emitted from different practical sources,it is quite necessary to develop multi-functional catalysts with desirable adsorption-catalysis activity,so as to meet the requirements from different cases ; in addition,the investigation of photocatalysis of CO2,and the characterization and simulation on the process of photosynthesis are beneficial to both the utilization of new energy and the mitigation of greenhouse gas.%随着全球化低碳经济时代的开启,温室气体的减排及利用成为举世关注的焦点,二氧化碳资源化利用及由此形成的新的碳一化学将成为绿色催化研究领域的热点问题.本文综述了二氧化碳资源化催化转化为高附加值化学品的若干反应途径,包括二氧化碳氧化饱和烃类、二氧化碳合成有

  19. Coal 99; Kol 99

    Energy Technology Data Exchange (ETDEWEB)

    Sparre, C.

    2000-07-01

    in equipment for burning pellets instead of coal. In Linkoeping waste of rubber is mixed with coal. Also Soederenergi AB has rebuilt their three coal boilers and replaced 100 % of the coal by peat and wood fuels. Coal is a reserve fuel. Several co-generation plants like Linkoeping, Norrkoeping, Uppsala and Oerebro use both coal and forest fuels. The use of coal is then concentrated to the electricity production. The average price of steam coal imported in Sweden in 1998 was 370 SEK/ton or the same as in 1997. For the world, the average import price fell about 6 USD/ton to 32 USD/ton. The price fall was concentrated to the 4th quarter. The prices have continued to fall during 1999 as a result of the crisis in Asia but are now stabilising as a result of increasing oil prices. All Swedish plants meet their emission limits of dust, SO{sub 2} and NO{sub x}, given by county administrations or concession boards. The co-generation plants have all some sort of SO{sub 2}-removal system. Mostly used is the wet-dry method. The biggest co-generation plant, in Vaesteraas, has recently invested in a catalytic NO{sub x}-cleaning system type SCR, which is reducing the emission level 80-90 %. Most other plants are using low NO{sub x}- burners or injection systems type SNCR, based on ammonium or urea, which are reducing the emissions 50-70 %. A positive effect of the recently introduced NO{sub x}-duties is a 60 % reduction compared to some years ago, when the duties were introduced. World hard coal production was about 3 700 tons in 1998, a minor decrease compared to 1997. The trade, however, has increased about 3 % to 520 mill tons. The coal demand in the OECD-countries has increased about 1,7 % yearly during the last ten years. The coal share of the energy supply is about 20% in the OECD-countries and 27% in the whole world. Several sources estimate a continuing growth during the next 20 years in spite of an increasing use of natural gas and nuclear power. The reason is a strong

  20. Coal gasification. Quarterly report, April--June 1977

    Energy Technology Data Exchange (ETDEWEB)

    None

    1978-01-01

    The conversion of coal to high-Btu gas requires a chemical and physical transformation of solid coal. However, because coal has widely differing chemical and physical properties, depending on where it is mined, it is difficult to process. Therefore, to develop the most suitable techniques for gasifying coal, ERDA, together with the American Gas Association, is sponsoring the development of several advanced conversion processes. Although the basic coal-gasification chemical reactions are the same for each process, the processes under development have unique characteristics. A number of the processes for converting coal to high Btu and to low Btu gas have reached the pilot plant stage. The responsibility for designing, constructing and operating each of these pilot plants is defined and progress on each during the quarter is described briefly. The accumulation of data for a coal gasification manual and the development of mathematical models of coal gasification processes are reported briefly. (LTN)

  1. Study on coal pyrolysis in Ar/H{sub 2} plasma jet

    Energy Technology Data Exchange (ETDEWEB)

    Chen, H.G.; Tian, Y.J.; Li, F.; Zhu, S.Y.; Xie, K.C. [Taiyuan University of Technology, Taiyuan (China). Shanxi Key Lab of Coal Science and Technology

    1999-07-01

    Hydrogen/Ar plasma jet was used to convert coal into acetylene. The efficiency of conversion depended on factors such as size range of coal particles, volatile matter and operating conditions. Coals had different acetylene selectivity which may depend on coal structure. 5 refs., 3 tabs.

  2. Thermocatalytical processing of coal and shales

    Directory of Open Access Journals (Sweden)

    Zhaksyntay Kairbekov

    2012-12-01

    Full Text Available The article investigates the questions of thermocatalytical conversion of organic mass of coal (OMC, it is shown that in the absence of a catalyst process is carried out by a radical process. Accumulated data on the properties for radicals of different structure and therefore different reaction capacity enables us to understand and interpret the conversion of OMC. Thermal conversion of OMC regarded as a kind of depolymerization, accompanied by decomposition of the functional groups with the formation of radicals, competing for hydrogen atom. Catalyst can change the direction and conditions of the process. Modern catalysts can reduce the process pressure up to 50 atm., with a high degree of coal conversion. We consider examples of simultaneous conversion of coal and shale, shale and masut, shale and tar.

  3. Les procédés ASVAHL thermiques et catalytiques sous pression d'hydrogène pour la conversion des bruts lourds et des résidus de bruts classiques Thermal and Catalytic Asvahl Processes under Hydrogen Pressure for Converting Heavy Crudes and Conventional Residues

    Directory of Open Access Journals (Sweden)

    Peries J. P.

    2006-11-01

    Full Text Available Cet article décrit les performances comparées des procédés ASVAHL thermiques (TERVAHL T, TERVAHL H, TERVAHL HC et catalytiques (HYVAHL F, HYVAHL C dans deux cas de traitement: - brut désessencié Boscan (base des études objectif Transport; - résidu sous vide Safaniya (base des études Raffinage de résidu. A travers ces résultats, l'importance de la quantité d'hydrogène fixée est mise en évidence. Elle joue sur la conversion obtenue et sur la qualité des résidus. L'introduction de catalyseur soluble ou en suspension catalytique TERVAHL HC (hydroviscoréduction catalytique ou l'utilisation d'un catalyseur supporté (hydrotraiternent HYVAHL favorisent l'activation de l'hydrogène. C'est la combinaison des réactions de craquage, de polycondensation et d'hydrogénation, et les conditions opératoires (températures, temps de séjour et pression qui définiront les limites de la conversion pour une stabilité donnée des résidus. This article describes the comparative performances of thermal ASVAHL processes (TERVAHL T, TERVAHL H, TERVAHL HQ and catalytic ASVAHL processes (HYVAHL F, HYVAHL C for two types of processing: (1 degasolined Boscan crude (basis of studies for transportation feasibility, and (2 Safaniya vacuum residue (basis of studies for residue refining. The results reveal the importance of the amount of fixed hydrogen, which affects the conversion obtained and the quality of the residues. The introduction of a TERVAHL HC soluble catalyst or one in catalytic suspension (catalytic hydrovisbreaking or the use of a supported catalyst (HYVAHL hydrotreatment enhances the activation of hydrogen. The combination of cracking, polycondensation and hydrogen reactions together with the operating conditions (temperatures, residence time and pressure are what will define the conversion limits for a given stability of residues.

  4. Coal 99; Kol 99

    Energy Technology Data Exchange (ETDEWEB)

    Sparre, C.

    2000-07-01

    in equipment for burning pellets instead of coal. In Linkoeping waste of rubber is mixed with coal. Also Soederenergi AB has rebuilt their three coal boilers and replaced 100 % of the coal by peat and wood fuels. Coal is a reserve fuel. Several co-generation plants like Linkoeping, Norrkoeping, Uppsala and Oerebro use both coal and forest fuels. The use of coal is then concentrated to the electricity production. The average price of steam coal imported in Sweden in 1998 was 370 SEK/ton or the same as in 1997. For the world, the average import price fell about 6 USD/ton to 32 USD/ton. The price fall was concentrated to the 4th quarter. The prices have continued to fall during 1999 as a result of the crisis in Asia but are now stabilising as a result of increasing oil prices. All Swedish plants meet their emission limits of dust, SO{sub 2} and NO{sub x}, given by county administrations or concession boards. The co-generation plants have all some sort of SO{sub 2}-removal system. Mostly used is the wet-dry method. The biggest co-generation plant, in Vaesteraas, has recently invested in a catalytic NO{sub x}-cleaning system type SCR, which is reducing the emission level 80-90 %. Most other plants are using low NO{sub x}- burners or injection systems type SNCR, based on ammonium or urea, which are reducing the emissions 50-70 %. A positive effect of the recently introduced NO{sub x}-duties is a 60 % reduction compared to some years ago, when the duties were introduced. World hard coal production was about 3 700 tons in 1998, a minor decrease compared to 1997. The trade, however, has increased about 3 % to 520 mill tons. The coal demand in the OECD-countries has increased about 1,7 % yearly during the last ten years. The coal share of the energy supply is about 20% in the OECD-countries and 27% in the whole world. Several sources estimate a continuing growth during the next 20 years in spite of an increasing use of natural gas and nuclear power. The reason is a strong

  5. Review of the literature on leachates from coal storage piles

    Energy Technology Data Exchange (ETDEWEB)

    Davis, E.C.; Boegly, W.J. Jr.

    1978-01-01

    Runoff from coal storage piles associated with coal conversion or combustion facilities may represent a potential source of environmental pollution. This report is an assessment of existing information on coal pile leachate. The assessment indicates that few detailed studies have been conducted to date, and these are limited and the results are highly variable. More detailed long-range studies using various types of coal are recommended. These studies should be carried out both in the laboratory and in field-scale experiments.

  6. Effectiveness factors for hydroprocessing of coal and coal liquids

    Energy Technology Data Exchange (ETDEWEB)

    Massoth, F.E.; Seader, J.D.

    1990-01-01

    The aim of this research project is to develop a methodology to predict, from a knowledge of feed and catalyst properties, effectiveness factors for catalytic hydroprocessing of coal and coal liquids. To achieve this aim, it is necessary to account for restrictive diffusion, which has not hitherto been done from a fundamental approach under reaction conditions. The research proposed here entails a study of hydrodenitrogenation of model compounds and coal-derived liquids using three NiMo/alumina catalysts of different pore size to develop, for restrictive diffusion, a relationship that can be used for estimating reliable effectiveness factors. The program is divided into four parts: measurements of pertinent properties of the catalysts and of a coal liquid and its derived boiling-point cuts; determination of effective diffusivities and tortuosities of the catalysts; development of restrictive diffusion correlations from data on model N-compounds at reaction conditions; and testing of correlations with coal-liquid cuts and whole coal-liquid feed, modifying correlations as necessary.

  7. Effectiveness factors for hydroprocessing of coal and coal liquids

    Energy Technology Data Exchange (ETDEWEB)

    Massoth, F.E.; Seader, J.D.

    1990-03-29

    The aim of this project is to develop a methodology to predict, from a knowledge of feed and catalyst properties, effectiveness factors for catalytic hydroprocessing of coal and coal liquids. To achieve this aim, it is necessary to account for restrictive diffusion, which has not hitherto been done from a fundamental approach under reaction conditions. The research entails a study of hydrodenitrogenation of model compounds and coal-derived liquids using three NiMo/alumina catalysts of different pore size to develop, for restrictive diffusion, a relationship that can be used for estimating reliable effectiveness factors. The research program includes: Task A - measurement of pertinent properties of the catalysts and of several coal liquids; Task B - determination of effective diffusivities and turtuosities of the catalysts; Task C - development of restrictive diffusion correlations from data on model N-compound reactions; Task D - testing of correlations with coal-liquid cuts and whole coal-liquid feed. Results are presented and discussed from Tasks B and D. 9 refs., 6 figs., 4 tabs.

  8. Fundamental bioprocessing research for coal applications

    Energy Technology Data Exchange (ETDEWEB)

    Kaufman, E.N.

    1996-06-01

    The purpose of this program is to gain a fundamental understanding and sound scientific technical basis for evaluating the potential roles of innovative bioprocessing concepts for the utilization and conversion of coal. The aim is to explore the numerous ways in which advanced biological processes and techniques can open new opportunities for coal utilization or can replace more conventional techniques by use of milder conditions with less energy consumption or loss. There are several roles where biotechnology is likely to be important in coal utilization and conversion. These include potential bioprocessing systems such.

  9. Synthesis of a nano-crystalline solid acid catalyst from fly ash and its catalytic performance

    Energy Technology Data Exchange (ETDEWEB)

    Chitralekha Khatri; Ashu Rani [Government P.G. College, Kota (India). Environmental Chemistry Laboratory

    2008-10-15

    The synthesis of nano-crystalline activated fly ash catalyst (AFAC) with crystallite size of 12 nm was carried out by chemical and thermal treatment of fly ash, a waste material generated from coal-burning power plants. Fly ash was chemically activated using sulfuric acid followed by thermal activation at 600{sup o}C. The variation of surface and physico-chemical properties of the fly ash by activation methods resulted in improved acidity and therefore, catalytic activity for acid catalyzed reactions. The AFAC was characterized by X-ray diffraction, FT-IR spectroscopy, N{sub 2}-adsorption-desorption isotherm, scanning electron microscopy, flame atomic absorption spectrophotometry and sulfur content by CHNS/O elemental analysis. It showed amorphous nature due to high silica content (81%) and possessed high BET surface area (120 m{sup 2}/g). The catalyst was found to be highly active solid acid catalyst for liquid phase esterification of salicylic acid with acetic anhydride and methanol giving acetylsalicylic acid and methyl salicylate respectively. A maximum yield of 97% with high purity of acetylsalicylic acid (aspirin) and a very high conversion 87% of salicylic acid to methyl salicylate (oil of wintergreen) was obtained with AFAC. The surface acidity and therefore, catalytic activity in AFAC was originated by increased silica content, hydroxyl content and higher surface area as compared to fly ash. The study shows that coal generated fly ash can be converted into potential solid acid catalyst for acid catalyzed reactions. Furthermore, this catalyst may replace conventional environmentally hazardous homogeneous liquid acids making an ecofriendly; solvent free, atom efficient, solid acid based catalytic process. 27 refs., 5 figs., 2 tabs.

  10. COAL GEOLOGY

    Institute of Scientific and Technical Information of China (English)

    2014-01-01

    <正>20141574 Chen Hao(Exploration and Development Research Institute,Daqing Oilfield Company,Daqing 163712,China)High-Resolution Sequences and Coal Accumulating Laws in Nantun Formation of Huhe Lake Sag(Petroleum Geology&Oilfield Development in Daqing,ISSN1000-3754,CN23-1286/TQ,32(4),2013,p.15-19,5 illus.,15 refs.)Key words:coal accumulation regularity,coal

  11. COAL GEOLOGY

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    <正>20091159 Gao Yan(No.3 Prospecting Team of Anhui Bureau of Coal Geology,Suzhou 234000,China) Effect of Depositional Environment of Coal-Bearing Stratum on Major Coal Seams in Suntan Coalmine,Anhui Province(Geology of Anhui,ISSN 1005- 6157,CN34-1111/P,18(2),2008,p.114 -117,5 illus.,1 ref.,with English abstract)

  12. Coal fires in Indonesia

    Energy Technology Data Exchange (ETDEWEB)

    Whitehouse, Alfred E.; Mulyana, Asep A.S. [Office of Surface Mining/Ministry of Energy and Mineral Resources Coal Fire Project, Ministry of Energy and Mineral Resources, Agency for Training and Education, Jl. Gatot Subroto, Kav. 49, Jakarta 12950 (Indonesia)

    2004-07-12

    Indonesia's fire and haze problem is increasingly being ascribed to large-scale forest conversion and land clearing activities making way for pulpwood, rubber and oil palm plantations. Fire is the cheapest tool available to small holders and plantation owners to reduce vegetation cover and prepare and fertilize extremely poor soils. Fires that escaped from agricultural burns have ravaged East Kalimantan forests on the island of Borneo during extreme drought periods in 1982-1983, 1987, 1991, 1994 and 1997-1998. Estimates based on satellite data and ground observations are that more than five million hectares were burned in East Kalimantan during the 1997/1998 dry season. Not only were the economic losses and ecological damage from these surface fires enormous, they ignited coal seams exposed at the ground surface along their outcrops.Coal fires now threaten Indonesia's shrinking ecological resources in Kutai National Park and Sungai Wain Nature Reserve. Sungai Wain has one of the last areas of unburned primary rainforest in the Balikpapan-Samarinda area with an extremely rich biodiversity. Although fires in 1997/1998 damaged nearly 50% of this Reserve and ignited 76 coal fires, it remains the most valuable water catchment area in the region and it has been used as a reintroduction site for the endangered orangutan. The Office of Surface Mining provided Indonesia with the capability to take quick action on coal fires that presented threats to public health and safety, infrastructure or the environment. The US Department of State's Southeast Asia Environmental Protection Initiative through the US Agency for International Development funded the project. Technical assistance and training transferred skills in coal fire management through the Ministry of Energy and Mineral Resource's Training Agency to the regional offices; giving the regions the long-term capability to manage coal fires. Funding was also included to extinguish coal fires as

  13. Mechanisms and kinetics of coal hydrogenation

    Energy Technology Data Exchange (ETDEWEB)

    Baldwin, R M; Furlong, M W

    1981-05-01

    Colorado School of Mines is engaged in an experimental program to develop comprehensive models for the effects of coal composition upon the kinetics and mechanisms of coal hydrogenation, for the effects of mineral matter additives (disposable catalysts) upon kinetics and mechanisms of coal hydrogenation, and for the kinetics and mechanisms of the hydrogenation of coal derived products such as preasphaltenes, and asphaltenes. Experimental work was completed on a suite of bituminous coals, thus completing the initial phase of the coal reactivity study. Eleven of the 14 coals of the suite were successfully run in duplicate. Conversion to THF solubles was correlated well by pseudo-second order kinetics. The resulting kinetic rate constants correlated with H/C ratio, mean-max vitrinite reflectance, and a specially-defined fraction of reactive macerals. The data did not correlate well with O/C ratios of the parent coals. Computer-derived statistical fits of various kinetic models were limited in their effectiveness at fitting the experimental data. Experimental work on the first phase of the disposal catalyst studies was completed. Statistical significance testing of the experimental data showed: fractional conversion and yield of light hydrocarbon products increased with time; and mineral properties of the additives were more significant in increasing overall conversion than the additive surface areas. The relative effects of the additives are given.

  14. Catalytic cracking of lignites

    Energy Technology Data Exchange (ETDEWEB)

    Seitz, M.; Nowak, S.; Naegler, T.; Zimmermann, J. [Hochschule Merseburg (Germany); Welscher, J.; Schwieger, W. [Erlangen-Nuernberg Univ. (Germany); Hahn, T. [Halle-Wittenberg Univ., Halle (Germany)

    2013-11-01

    A most important factor for the chemical industry is the availability of cheap raw materials. As the oil price of crude oil is rising alternative feedstocks like coal are coming into focus. This work, the catalytic cracking of lignite is part of the alliance ibi (innovative Braunkohlenintegration) to use lignite as a raw material to produce chemicals. With this new one step process without an input of external hydrogen, mostly propylene, butenes and aromatics and char are formed. The product yield depends on manifold process parameters. The use of acid catalysts (zeolites like MFI) shows the highest amount of the desired products. Hydrogen rich lignites with a molar H/C ratio of > 1 are to be favoured. Due to primary cracking and secondary reactions the ratio between catalyst and lignite, temperature and residence time are the most important parameter to control the product distribution. Experiments at 500 C in a discontinuous rotary kiln reactor show yields up to 32 wt-% of hydrocarbons per lignite (maf - moisture and ash free) and 43 wt-% char, which can be gasified. Particularly, the yields of propylene and butenes as main products can be enhanced four times to about 8 wt-% by the use of catalysts while the tar yield decreases. In order to develop this innovative process catalyst systems fixed on beads were developed for an easy separation and regeneration of the used catalyst from the formed char. (orig.)

  15. Carbon cycle in advanced coal chemical engineering.

    Science.gov (United States)

    Yi, Qun; Li, Wenying; Feng, Jie; Xie, Kechang

    2015-08-07

    This review summarizes how the carbon cycle occurs and how to reduce CO2 emissions in highly efficient carbon utilization from the most abundant carbon source, coal. Nowadays, more and more attention has been paid to CO2 emissions and its myriad of sources. Much research has been undertaken on fossil energy and renewable energy and current existing problems, challenges and opportunities in controlling and reducing CO2 emission with technologies of CO2 capture, utilization, and storage. The coal chemical industry is a crucial area in the (CO2 value chain) Carbon Cycle. The realization of clean and effective conversion of coal resources, improving the utilization and efficiency of resources, whilst reducing CO2 emissions is a key area for further development and investigation by the coal chemical industry. Under a weak carbon mitigation policy, the value and price of products from coal conversion are suggested in the carbon cycle.

  16. Effects and characterization of an environmentally-friendly, inexpensive composite Iron-Sodium catalyst on coal gasification

    Science.gov (United States)

    Monterroso, Rodolfo

    Coal gasification has been commercially used for more than 60 years in the production of fuels and chemicals. Recently, and due to the lowered environmental impacts and high efficiency derived from integrated gasification combined cycle (IGCC), this process has received increased attention. Furthermore, upcoming strict CO2 emissions regulations by the U.S. Environmental Protection Agency (EPA) will no longer be achievable by traditional means of coal combustion, therefore, growing dependence on different energy sources has drawn attention to clean coal technologies, such as coal-to-liquids processing, and the core of this process is also gasification. Gasification is an energy intensive process that can be substantially improved in terms of efficiency through the use of catalysts. In this study, the effect of the composite catalyst, FeCO3-Na2CO3, on gasification of a low-sulfur sub-bituminous Wyodak coal from the Powder River Basin (PRB) of Wyoming was investigated. The catalytic effects of the composite catalysts were evaluated by comparing their effluent gas compositions and carbon conversion kinetics to those achieved in the presence of either FeCO3 or Na2CO3 catalyst alone or without the presence of any catalyst. All of the evaluation work was conducted in a fixed bed gasifier at atmospheric pressure. Compared to raw coal with no catalyst, the composite catalyst is efficient in increasing the carbon conversion rate constant by as much as two times within the 700-800°C range due to its ability to reduce the activation energy of gasification by about 30-40%. Compared to pure sodium and iron catalysts, the composite catalyst can increase the yields of desired products H2 and CO at 800°C by 15% and 40%, respectively. The composite catalyst can not only synergize the advantages, but also overcome the challenges of pure iron or pure sodium based catalytic coal gasification processes. Moreover, the mechanisms of this particular catalytic coal gasification process

  17. Design of Digital Voice Conversational Terminal of Coal Mine Based on LWIP%基于LWIP的煤矿数字语音对讲终端的设计

    Institute of Scientific and Technical Information of China (English)

    包建军; 徐炜; 罗克

    2011-01-01

    Based on analysis of function limitation of underground speak telephone system, a novel scheme of digital voice conversational terminal of coal mine with network interface based on open-source LWIP protocol stack was proposed, the terminal's application function, hardware composition and software model were introduced, the LWIP protocol stack and its transplanting to FreeRTOS embedded operating system were described, and design points of LWIP in applications layer of the terminal were analyzed. The terminal has functions of digital broadcasting and talkback, uses standard RTP protocol, and supports voice interaction with 8 kHz and 16 kHz sampling frequencies and on-line streaming broadcasting of MP3 with up to 44. 1 kHz sampling frequency. Feasibility and effectiveness of the scheme were verified by experiment results.%在分析井下扩音电话系统功能局限性的基础上,提出了基于开源的LWIP协议栈设计一种具有网络接口的煤矿数字语音对讲终端的方案,详细介绍了该终端的功能、硬件组成和软件模块;阐述了LWIP协议栈及其在嵌入式操作系统FreeRTOS上的移植,继而分析了LWIP在该终端应用层的设计要点.该终端具备数字扩音广播与对讲功能;采用标准RTP协议,既支持采样频率为8 kHz、16 kHz的话音交互,也支持采样频率高达44.1 kHz的MP3等流媒体在线播放.实验结果验证了该方案的可行性和有效性.

  18. Catalytic Upgrading of Sugars to Hydrocarbons Technology Pathway

    Energy Technology Data Exchange (ETDEWEB)

    Biddy, M.; Jones, S.

    2013-03-01

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

  19. COAL GEOLOGY

    Institute of Scientific and Technical Information of China (English)

    2013-01-01

    <正>20131668 Chang Huizhen(Key Laboratory of Coalbed Methane Resources and Reservoir Formation Process,CUMT,Ministry of Edu-cation,School of Resource and Earth Science,China University of Mining and Technology,Xuzhou 221008,China);Qin Yong Differences in of Pore Structure of Coals and Their Impact on the Permeability of Coals from the

  20. Actual development of the conversion of energy sources of minor value in so-called bio coal. A comparison of pyrolysis process with the HTC process; Aktuelle Entwicklung bei der Konversion von minderwertigen Energietraegern in die so genannte Biokohle. Ein Vergleich von Pyrolyse- und HTC-Verfahren

    Energy Technology Data Exchange (ETDEWEB)

    Neudeck, Diana; Roedger, Jan-Markus [HAWK Hochschule fuer angewandte Wissenschaft und Kunst, Goettingen (Germany); Loewen, Achim

    2012-07-01

    The conversion of biomass with low quality into biochar through pyrolysis or hydro-thermal carbonization is suitable to substitute lignite and hard coal as a fuel and thereby improve the carbon footprint of a firing plant: Additionally there is the possibility to apply biochar to fields. Carbon compounds, stabilized by the carbonization process, could simultaneously increase crop yields and sequester carbon for mid- and long term. This paper compares the two processes pyrolysis and hydrothermal carbonization regarding input-material, process-parameters, product-properties and possible applications for each product. The aim is to give an overview which process with given parameters leads to which final product and application. (orig.)

  1. Progress on Catalytic Conversion of Methane to Syngas in the Present of Oxygen%甲烷临氧催化转化制合成气研究进展

    Institute of Scientific and Technical Information of China (English)

    井强山; 刘鹏; 郑小明

    2008-01-01

      The preparation of synthesis gas from natural gas, which is the most important step in the gas-to-liquid transformation, has attracted increasing attention in the last decade. The varieties of synthesis gas technology by catalytic converting methane in the present of oxygen were introduced briefly. Authors’ work in preparation of syngas form methane in the present of oxygen is referred. The various processes including catalytic partial oxidation (CPO), auto-thermal CO2 reforming (ATR-CO2), auto-thermal H2O reforming (ATR-H2O) and tri-reforming of methane were reviewed. Achievements including catalyst, reaction mechanism and process conditions were discussed. The research focus and commercial application of catalytic converting methane in the future was also prospected as well.%  作为烃类液化的最重要的步骤,从天然气制合成气是近几十年催化科学研究的前沿和热点之一。结合笔者实验室的工作,本文介绍了国内外甲烷临氧催化转化制合成气的研究现状,对甲烷部分氧化、甲烷临氧二氧化碳重整、甲烷临氧水蒸气重整及甲烷-二氧化碳-水-氧气偶合重整进行了阐述和分析,综述了在催化剂体系、反应机理和工艺条件等方面取得的近期研究成果;并对甲烷临氧催化转化制合成气技术今后的研究重点及应用作了展望。

  2. KINETICS OF DIRECT OXIDATION OF H2S IN COAL GAS TO ELEMENTAL SULFUR

    Energy Technology Data Exchange (ETDEWEB)

    K.C. Kwon

    2004-01-01

    The direct oxidation of H{sub 2}S to elemental sulfur in the presence of SO{sub 2} is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S. This direct oxidation process has the potential to produce a super clean coal gas more economically than both conventional amine-based processes and the hot-gas desulfurization using regenerable metal oxide sorbents followed by Direct Sulfur Recovery Process. The objective of this research is to support the near- and long-term process development efforts to commercialize this direct oxidation technology. The objectives of this research are to measure kinetics of direct oxidation of H{sub 2}S to elemental sulfur in the presence of a simulated coal gas mixture containing SO{sub 2}, H{sub 2}, and moisture, using 160-{micro}m C-500-04 alumina catalyst particles and a micro bubble reactor, and to develop kinetic rate equations and model the direct oxidation process to assist in the design of large-scale plants. This heterogeneous catalytic reaction has gaseous reactants such as H{sub 2}S and SO{sub 2}. However, this heterogeneous catalytic reaction has heterogeneous products such as liquid elemental sulfur and steam. To achieve the above-mentioned objectives, experiments on conversion of hydrogen sulfide into liquid elemental sulfur were carried out for the space time range of 1-6 milliseconds at 125-155 C to evaluate effects of reaction temperature, moisture concentration, reaction pressure on conversion of hydrogen sulfide into liquid elemental sulfur. Simulated coal gas mixtures consist of 70 v% hydrogen, 2,500-7,500-ppmv hydrogen sulfide, 1,250-3,750 ppmv sulfur dioxide, and 0-15 vol% moisture, and nitrogen as remainder. Volumetric feed rates of a simulated coal gas mixture to a micro bubble reactor are 100 cm{sup 3}/min at room temperature and atmospheric pressure. The temperature of the reactor is controlled in an oven at 125-155 C. The

  3. KINETICS OF DIRECT OXIDATION OF H2S IN COAL GAS TO ELEMENTAL SULFUR

    Energy Technology Data Exchange (ETDEWEB)

    K.C. Kwon

    2005-01-01

    The direct oxidation of H{sub 2}S to elemental sulfur in the presence of SO{sub 2} is ideally suited for coal gas from commercial gasifiers with a quench system to remove essentially all the trace contaminants except H{sub 2}S. This direct oxidation process has the potential to produce a super clean coal gas more economically than both conventional amine-based processes and the hot-gas desulfurization using regenerable metal oxide sorbents followed by Direct Sulfur Recovery Process. The objective of this research is to support the near- and long-term process development efforts to commercialize this direct oxidation technology. The objectives of this research are to measure kinetics of direct oxidation of H{sub 2}S to elemental sulfur in the presence of a simulated coal gas mixture containing SO{sub 2}, H{sub 2}, and moisture, using 160-{micro}m C-500-04 alumina catalyst particles and a micro bubble reactor, and to develop kinetic rate equations and model the direct oxidation process to assist in the design of large-scale plants. This heterogeneous catalytic reaction has gaseous reactants such as H{sub 2}S and SO{sub 2}. However, this heterogeneous catalytic reaction has heterogeneous products such as liquid elemental sulfur and steam. To achieve the above-mentioned objectives, experiments on conversion of hydrogen sulfide into liquid elemental sulfur were carried out for the space time range of 0.059-0.87 seconds at 125-155 C to evaluate effects of reaction temperature, H{sub 2}S concentration, reaction pressure, and catalyst loading on conversion of hydrogen sulfide into liquid elemental sulfur. Simulated coal gas mixtures consist of 62-78 v% hydrogen, 3,000-7,000-ppmv hydrogen sulfide, 1,500-3,500 ppmv sulfur dioxide, and 10 vol % moisture, and nitrogen as remainder. Volumetric feed rates of a simulated coal gas mixture to a micro bubble reactor are 50 cm{sup 3}/min at room temperature and atmospheric pressure. The temperature of the reactor is controlled in an

  4. INVESTIGATION OF SELECTIVE CATALYTIC REDUCTION IMPACT ON MERCURY SPECIATION UNDER SIMULATED NOX EMISSION CONTROL CONDITIONS

    Science.gov (United States)

    Selective catalytic reduction (SCR) technology is being increasingly applied for controlling emissions of nitrogen oxides (NOx) from coal-fired boilers. Some recent field and pilot studies suggest that the operation of SCR could affect the chemical form of mercury in the coal com...

  5. Catalytic and thermal cracking processes of waste cooking oil for bio-gasoline synthesis

    Science.gov (United States)

    Dewanto, Muhammad Andry Rizki; Januartrika, Aulia Azka; Dewajani, Heny; Budiman, Arief

    2017-03-01

    Non-renewable energy resources such as fossil fuels, and coal were depleted as the increase of global energy demand. Moreover, environmental aspect becomes a major concern which recommends people to utilize bio-based resources. Waste cooking oil is one of the economical sources for biofuel production and become the most used raw material for biodiesel production. However, the products formed during frying, can affect the trans-esterification reaction and the biodiesel properties. Therefore, it needs to convert low-quality cooking oil directly into biofuel by both thermal and catalytic cracking processes. Thermal and catalytic cracking sometimes are regarded as prospective bio-energy conversion processes. This research was carried out in the packed bed reactor equipped with 2 stages preheater with temperature of reactor was variated in the range of 450-550°C. At the same temperature, catalytic cracking had been involved in this experiment, using activated ZSM-5 catalyst with 1 cm in length. The organic liquid product was recovered by three stages of double pipe condensers. The composition of cracking products were analyzed using GC-MS instrument and the caloric contents were analyzed using Bomb calorimeter. The results reveal that ZSM-5 was highly selective toward aromatic and long aliphatic compounds formation. The percentage recovery of organic liquid product from the cracking process varies start from 8.31% and the optimal results was 54.08%. The highest heating value of liquid product was resulted from catalytic cracking process at temperature of 450°C with value of 10880.48 cal/gr and the highest product yield with 54.08% recovery was achieved from thermal cracking process with temperature of 450°C.

  6. Effect of dry torrefaction on kinetics of catalytic pyrolysis of sugarcane bagasse

    Science.gov (United States)

    Daniyanto, Sutijan, Deendarlianto, Budiman, Arief

    2015-12-01

    Decreasing world reserve of fossil resources (i.e. petroleum oil, coal and natural gas) encourage discovery of renewable resources as subtitute for fossil resources. Biomass is one of the main natural renewable resources which is promising resource as alternate resources to meet the world's energy needs and raw material to produce chemical platform. Conversion of biomass, as source of energy, fuel and biochemical, is conducted using thermochemical process such as pyrolysis-gasification process. Pyrolysis step is an important step in the mechanism of pyrolysis - gasification of biomass. The objective of this study is to obtain the kinetic reaction of catalytic pyrolysis of dry torrified sugarcane bagasse which used Ca and Mg as catalysts. The model of kinetic reaction is interpreted using model n-order of single reaction equation of biomass. Rate of catalytic pyrolysis reaction depends on the weight of converted biomass into char and volatile matters. Based on TG/DTA analysis, rate of pyrolysis reaction is influenced by the composition of biomass (i.e. hemicellulose, cellulose and lignin) and inorganic component especially alkali and alkaline earth metallic (AAEM). From this study, it has found two equations rate of reaction of catalytic pyrolysis in sugarcane bagasse using catalysts Ca and Mg. First equation is equation of pyrolysis reaction in rapid zone of decomposition and the second equation is slow zone of decomposition. Value of order reaction for rapid decomposition is n > 1 and for slow decomposition is nConstant and order of reactions for catalytic pyrolysis of dry-torrified sugarcane bagasse with presence of Ca tend to higher than that's of presence of Mg.

  7. CO2催化转化为高附加值燃料:现状、挑战及其未来方向%Catalytic conversion of CO2 to value added fuels:Current status, challenges, and future directions

    Institute of Scientific and Technical Information of China (English)

    Jingjie Wu; Xiao-Dong Zhou

    2016-01-01

    The electrochemical reduction of CO2 into liquid fuels especially coupling with the intermittent renewable electricity offers a promising means of storing electricity in chemical form, which reduc‐es the dependence on fossil fuels and mitigates the negative impact of anthropogenic CO2 emissions on the planet. Although converting CO2 to fuels is not in itself a new concept, the field has not sub‐stantially advanced in the last 30 years primarily because of the challenge of discovery of structural electrocatalysts and the development of membrane architectures for efficient collection of reactants and separation of products. This overview summarizes recent advances in catalytic conversion of CO2 and presents the challenges and future directions in producing value‐added fuels.

  8. Fluidized-bed bioreactor system for the microbial solubilization of coal

    Science.gov (United States)

    Scott, C.D.; Strandberg, G.W.

    1987-09-14

    A fluidized-bed bioreactor system for the conversion of coal into microbially solubilized coal products. The fluidized-bed bioreactor continuously or periodically receives coal and bio-reactants and provides for the production of microbially solubilized coal products in an economical and efficient manner. An oxidation pretreatment process for rendering coal uniformly and more readily susceptible to microbial solubilization may be employed with the fluidized-bed bioreactor. 2 figs.

  9. Fixed-bed bioreactor system for the microbial solubilization of coal

    Science.gov (United States)

    Scott, C.D.; Strandberg, G.W.

    1987-09-14

    A fixed-bed bioreactor system for the conversion of coal into microbially solubilized coal products. The fixed-bed bioreactor continuously or periodically receives coal and bio-reactants and provides for the large scale production of microbially solubilized coal products in an economical and efficient manner. An oxidation pretreatment process for rendering coal uniformly and more readily susceptible to microbial solubilization may be employed with the fixed-bed bioreactor. 1 fig., 1 tab.

  10. Fluidized-bed bioreactor process for the microbial solubiliztion of coal

    Science.gov (United States)

    Scott, Charles D.; Strandberg, Gerald W.

    1989-01-01

    A fluidized-bed bioreactor system for the conversion of coal into microbially solubilized coal products. The fluidized-bed bioreactor continuously or periodically receives coal and bio-reactants and provides for the production of microbially solubilized coal products in an economical and efficient manner. An oxidation pretreatment process for rendering coal uniformly and more readily susceptible to microbial solubilization may be employed with the fluidized-bed bioreactor.

  11. Application of Fischer–Tropsch Synthesis in Biomass to Liquid Conversion

    Directory of Open Access Journals (Sweden)

    Yongwu Lu

    2012-06-01

    Full Text Available Fischer–Tropsch synthesis is a set of catalytic processes that can be used to produce fuels and chemicals from synthesis gas (mixture of CO and H2, which can be derived from natural gas, coal, or biomass. Biomass to Liquid via Fischer–Tropsch (BTL-FT synthesis is gaining increasing interests from academia and industry because of its ability to produce carbon neutral and environmentally friendly clean fuels; such kinds of fuels can help to meet the globally increasing energy demand and to meet the stricter environmental regulations in the future. In the BTL-FT process, biomass, such as woodchips and straw stalk, is firstly converted into biomass-derived syngas (bio-syngas by gasification. Then, a cleaning process is applied to remove impurities from the bio-syngas to produce clean bio-syngas which meets the Fischer–Tropsch synthesis requirements. Cleaned bio-syngas is then conducted into a Fischer–Tropsch catalytic reactor to produce green gasoline, diesel and other clean biofuels. This review will analyze the three main steps of BTL-FT process, and discuss the issues related to biomass gasification, bio-syngas cleaning methods and conversion of bio-syngas into liquid hydrocarbons via Fischer–Tropsch synthesis. Some features in regard to increasing carbon utilization, enhancing catalyst activity, maximizing selectivity and avoiding catalyst deactivation in bio-syngas conversion process are also discussed.

  12. Effect of cobalt and its adding sequence on the catalytic performance of MoO3/Al2O3 toward sulfur-resistant methanation

    Institute of Scientific and Technical Information of China (English)

    Baowei; Wang; Yuqin; Yao; Minhong; Jiang; Zhenhua; Li; Xinbin; Ma; Shaodong; Qin; Qi; Sun

    2014-01-01

    The effect of promoter cobalt and the sequences of adding cobalt and molybdenum precursors on the performance of sulfur-resistant methanation were investigated. All these samples were prepared by impregnation method and characterized by N2-adsorption, X-ray diffraction(XRD), temperature-programmed reduction(TPR) and laser Raman spectroscopy(LRS). The conversions of CO for Mo-Co/Al, Co-Mo/Al and CoMo/Al catalysts were 59.7%, 54.3% and 53.9%, respectively. Among these catalysts, the Mo-Co/Al catalyst prepared stepwisely by impregnating Mo precursor firstly showed the best catalytic performance. Meanwhile, the conversions of CO were 48.9% for Mo/Al catalyst and 10.5% for Co/Al catalyst. The addition of cobalt species could improve the catalytic activity of Mo/Al catalyst. The N2-adsorption results showed that Co-Mo/Al catalyst had the smallest specific surface area among these catalysts. CoMoO4species in CoMo/Al catalyst were detected with XRD, TPR and LRS. Moreover, crystal MoS2which was reported to be less active than amorphous MoS2was found in both Co-Mo/Al and CoMo/Al catalysts. Mo-Co/Al catalyst showed the best catalytic performance as it had an appropriate surface structure, i.e., no crystal MoS2and very little CoMoO4species.

  13. COAL GEOLOGY

    Institute of Scientific and Technical Information of China (English)

    2011-01-01

    <正>20111053 Chen Jian(School of Earth and Environment,Anhui University of Science and Technology,Huainan 232001,China);Liu Wenzhong Organic Affinity of Trace Elements in Coal from No.10 Coal-Bed at Western Huagou,Guoyang(Coal Geology & Exploration,ISSN1001-1986,CN61-1155/P,38(4),2010,p.16-20,24,3 illus.,3 tables,19 refs.)Key words:coal,minor elements,Anhui Province In order to study the organic affinity of trace elements in coal from No.10 coal-bed at western Huagou,Guoyang,10 borehole samples were collected at exploration area of Huaibei mining area.The contents of 12 kinds of trace elements were determined by the inductively coupled plasma mass spectrometry(ICP-MS),the total organic carbon(TOC)of coal was determined by LECO carbon and sulfur analyzer,and the organic affinity of trace elements were deduced from the correlations between contents and TOCs.The results showed that the contents of V,Cr,Co,Ni,Mo,Cd,Sb,Pb and Zn were lower than

  14. 20 CFR 404.1084 - Gain or loss from disposition of property; capital assets; timber, coal, and iron ore...

    Science.gov (United States)

    2010-04-01

    ...; capital assets; timber, coal, and iron ore; involuntary conversion. 404.1084 Section 404.1084 Employees... from disposition of property; capital assets; timber, coal, and iron ore; involuntary conversion. (a... capital asset; (2) From the cutting of timber or from the disposal of timber or coal, even if...

  15. Catalytic and Gas-Solid Reactions Involving HCN over Limestone

    DEFF Research Database (Denmark)

    Jensen, Anker; Johnsson, Jan Erik; Dam-Johansen, Kim

    1997-01-01

    In coal-fired combustion systems solid calcium species may be present as ash components or limestone added to the combustion chamber. In this study heterogeneous reactions involving HCN over seven different limestones were investigated in a laboratory fixed-bed quartz reactor at 873-1,173 K....... Calcined limestone is an effective catalyst for oxidation of HCN. Under conditions with complete conversion of HCN at O-2 concentrations above about 5,000 ppmv the selectivity for formation of NO and N2O is 50-70% and below 5%, respectively. Nitric oxide can be reduced by HCN to N-2 in the absence of O-2...... and to N-2 and N2O in the presence of O-2. At low O-2 concentrations or low temperatures. HCN may react with CaO, forming calcium cyanamide, CaCN2. The selectivities for formation of NO and N2O from oxidation of CaCN2 is 20-25% for both species. The catalytic activity of limestone for oxidation of HCN...

  16. Coal gasification with water under supercritical conditions

    Energy Technology Data Exchange (ETDEWEB)

    A.A. Vostrikov; S.A. Psarov; D.Yu. Dubov; O.N. Fedyaeva; M.Ya. Sokol [Russian Academy of Sciences, Novosibirsk (Russian Federastion). Kutateladze Institute of Thermophysics, Siberian Division

    2007-08-15

    The conversion of an array of coal particles in supercritical water (SCW) was studied in a semibatch reactor at a pressure of 30 MPa, 500-750{sup o}C, and a reaction time of 1-12 min. The bulk conversion, surface conversion, and random pore models were used to describe the conversion. The quantitative composition of reaction products was determined, and the dependence of the rate of reaction on the degree of coal conversion, reaction time, and reaction temperature was obtained on the assumption of a first-order reaction and the Arrhenius function. It was found that the gasification of coal under SCW conditions without the addition of oxidizing agents is a weakly endothermic process. The addition of CO{sub 2} to SCW decreased the rate of conversion and increased the yield of CO. It was found that, at a 90% conversion of the organic matter of coal (OMC) in a flow of SCW in a time of 2 min, the process power was 26 W/g per gram of OMC.

  17. Contentious Conversations

    Science.gov (United States)

    Zuidema, Leah A.

    2011-01-01

    The idea of joining a conversation through reading and writing is not new; in his 1941 book "The Philosophy of Literary Form: Studies in Symbolic Action," Kenneth Burke suggests that the acts of reading and writing are like entering a parlor where others are already conversing. The author explores the place of professional debate within NCTE and…

  18. Conversational Narcissism.

    Science.gov (United States)

    Vangelisti, Anita L.; And Others

    1990-01-01

    Examines narcissistic communication and the ways it is exhibited in everyday conversation. Identifies the following behavioral referents: boasting, refocusing the topic of conversation on the self, exaggerating hand and body movements, using a loud tone of voice, and "glazing over" when others speak. Suggests that conversational…

  19. Investigation on CO catalytic oxidation reaction kinetics of faceted perovskite nanostructures loaded with Pt

    KAUST Repository

    Yin, S. M.

    2017-01-18

    Perovskite lead titanate nanostructures with specific {111}, {100} and {001} facets exposed, have been employed as supports to investigate the crystal facet effect on the growth and CO catalytic activity of Pt nanoparticles. The size, distribution and surface chemical states of Pt on the perovskite supports have been significantly modified, leading to a tailored conversion temperature and catalytic kinetics towards CO catalytic oxidation.

  20. Cooperative research program in coal liquefaction. Quarterly report, May 1, 1993--October 31, 1993

    Energy Technology Data Exchange (ETDEWEB)

    Hoffman, G.P. [ed.

    1994-07-01

    This report summarizes progress in four areas of research under the general heading of Coal Liquefaction. Results of studies concerning the coliquefaction of coal with waste organic polymers or chemical products of these polymers were reported. Secondly, studies of catalytic systems for the production of clean transportation fuels from coal were discussed. Thirdly, investigations of the chemical composition of coals and their dehydrogenated counterparts were presented. These studies were directed toward elucidation of coal liquefaction processes on the chemical level. Finally, analytical methodologies developed for in situ monitoring of coal liquefaction were reported. Techniques utilizing model reactions and methods based on XAFS, ESR, and GC/MS are discussed.

  1. The Effect of Alkali Carbonate on the Catalytic Properties for Methane Conversion with Ce-Zr-O%碱金属碳酸盐掺杂的Ce-Zr-O对甲烷转化催化性能的影响

    Institute of Scientific and Technical Information of China (English)

    段月娟; 魏永刚; 李孔斋; 王华; 祝星; 杜云鹏

    2012-01-01

    Pure Ce-Zr-O mixed oxide was prepared via precipitation method, and catalysts doped with alkali carbonates (M2CO3, M=Li, Na, K) were prepared by incipient wetness impregnation methods. The catalytic activity for methane was investigated by the gas-solid reaction in a fixed bed reactor, and characterized by means of XRD and H2-TPR techniques. The results show that the catalytic activity of Ce-Zr-O is promoted with varied following the doping of alkali carbonates, the anti-coking and anti-sintering properties of the catalysts are enhanced, and the surface oxygen species and the bulk oxygen species of the catalysts are improved as well.%采用共沉淀法制备了Ce-Zr-O载体,通过等体积浸渍法得到碱金属碳酸盐掺杂的M2CO3/Ce-Zr-O(M=Li,Na,K)催化剂.采用自制的小型固定床反应器考察了催化剂的甲烷转化催化活性,并利用XRD和H2-TPR对催化剂进行了表征.研究结果表明,碱金属碳酸盐的添加均不同程度地提高了Ce-Zr-O催化剂的催化活性、抗积碳性能和抗烧结性能,还改善了催化剂表面氧物种和体相氧物种的氧化还原性能.

  2. Literature survey of properties of synfuels derived from coal

    Science.gov (United States)

    Reynolds, T. W.; Niedzwiecki, R. W.; Clark, J. S.

    1980-02-01

    A literature survey of the properties of synfuels for ground-based gas turbine applications is presented. Four major concepts for converting coal into liquid fuels are described: solvent extraction, catalytic liquefaction, pyrolysis, and indirect liquefaction. Data on full range syncrudes, various distillate cuts, and upgraded products are presented for fuels derived from various processes, including H-coal, synthoil, solvent-refined coal, donor solvent, zinc chloride hydrocracking, co-steam, and flash pyrolysis. Some typical ranges of data for coal-derived low Btu gases are also presented.

  3. Energy Saving and Pollution Reducing Effects of Coal Combustion Catalysts

    Institute of Scientific and Technical Information of China (English)

    WU Zenghua; YU Zhiwu; ZHU Wentao; ZHOU Rui

    2001-01-01

    Coal catalytic agents (CCS type) have been prepared to improve coal combustion and reduce air pollution.The energy and pollution reductions resulting from the catalysts have been examined with thermal analysis and chromatography.The CCS agents lower the ignition temperature by 30-80℃ and improve the coal combustion efficiency by 10%-25%.The agents also reduce the release of carbon monoxide,sulfur dioxide,and coal particles to environment.The working mechanisms of the catalysts are discussed in terms of their participation in various physico-chemical processes during combustion.

  4. Rosebud SynCoal Partnership, SynCoal{reg_sign} demonstration technology update

    Energy Technology Data Exchange (ETDEWEB)

    Sheldon, R.W. [Rosebud SynCoal Partnership, Billings, MT (United States)

    1997-12-31

    An Advanced Coal Conversion Process (ACCP) technology being demonstrated in eastern Montana (USA) at the heart of one of the world`s largest coal deposits is providing evidence that the molecular structure of low-rank coals can be altered successfully to produce a unique product for a variety of utility and industrial applications. The product is called SynCoal{reg_sign} and the process has been developed by the Rosebud SynCoal Partnership (RSCP) through the US Department of Energy`s multi-million dollar Clean Coal Technology Program. The ACCP demonstration process uses low-pressure, superheated gases to process coal in vibrating fluidized beds. Two vibratory fluidized processing stages are used to heat and convert the coal. This is followed by a water spray quench and a vibratory fluidized stage to cool the coal. Pneumatic separators remove the solid impurities from the dried coal. There are three major steps to the SynCoal{reg_sign} process: (1) thermal treatment of the coal in an inert atmosphere, (2) inert gas cooling of the hot coal, and (3) removal of ash minerals. When operated continuously, the demonstration plant produces over 1,000 tons per day (up to 300,000 tons per year) of SynCoal{reg_sign} with a 2% moisture content, approximately 11,800b Btu/lb and less than 1.0 pound of SO{sub 2} per million Btu. This product is obtained from Rosebud Mine sub-bituminous coal which starts with 25% moisture, 8,600 Btu/lb and approximately 1.6 pounds of SO{sub 2} per million Btu.

  5. Coal mining: coal in Spain

    Energy Technology Data Exchange (ETDEWEB)

    Garcia-Arguelles Martinez, A.; Lugue Cabal, V.

    1984-01-01

    The Survey of Spanish Coal Resources published by the Centre for Energy Studies in 1979 is without doubt the most serious and full study on this subject. The coal boom of the last few years and the important role it will play in the future, as well as the wealth of new information which has come to light in the research carried out in Spanish coalfields by both the public and private sector, prompted the General Mine Management of the Ministry of Industry and Energy to commission IGME to review and update the previous Survey of Spanish Coal Resources of November 1981.

  6. NMR potentials for studying physical processes in fossil coals

    Energy Technology Data Exchange (ETDEWEB)

    Alekseev, Anatolii D; Ul' yanova, Ekaterina V; Vasilenko, Tat' yana A [Institute of Mining Processes Physics, National Academy of Sciences of Ukraine, Donetsk (Ukraine)

    2005-11-30

    High-resolution, pulsed, and wide-line NMR studies of fossil coals are reviewed. Coal substance conversion due to outbursts is discussed. Results on water and methane interactions with coal substance, which provide insight into the dynamic characteristics of boundary water, the location of methane in coal structure, and water and methane's hazard implications for coal beds (gas- or geodynamic phenomena) are presented; these are shown to have potential for predicting and preventing life threatening situations. (instruments and methods of investigation)

  7. Blended coals for improved coal water slurries

    Institute of Scientific and Technical Information of China (English)

    GU Tian-ye; WU Guo-guang; LI Qi-hui; SUN Zhi-qiang; ZENG Fang; WANG Guang-you; MENG Xian-liang

    2008-01-01

    Three coal samples of different ranks were used to study the effect of coal blending on the preparation of Coal Water Slurry (CWS). The results show that by taking advantage of two kinds of coal, the coal concentration in slurry made from hard-to-pulp coal can be effectively improved and increased by 3%-5% generally. DLT coal (DaLiuTa coal mine) is very poor in slurryability and the stability and rheology of the resulting slurry are not very good. When the amount of easily slurried coal is more than 30%, all properties of the CWS improve and the CWS meets the requirements for use as fuel. Coalification, porosity, surface oxygenic functional groups, zeta potential and grindability have a great effect on the performance of blended coal CWS. This leads to some differences in performance between the slurry made from a single coal and slurry made from blended coal.

  8. Utilization and mitigation of VAM/CMM emissions by a catalytic combustion gas turbine

    Energy Technology Data Exchange (ETDEWEB)

    Tanaka, K.; Yoshino, Y.; Kashihara, H. [Kawasaki Heavy Industries Ltd., Hyougo (Japan); Kajita, S.

    2013-07-01

    A system configured with a catalytic combustion gas turbine generator unit is introduced. The system has been developed using technologies produced by Kawasaki Heavy Industries, Ltd., such as small gas turbines, recuperators and catalytic combustors, and catalytic oxidation units which use exhaust heat from gas turbines. The system combusts (oxidizes) ventilation air methane (less than 1% concentration) and low concentration coal mine methane (30% concentration or less) discharged as waste from coal mines. Thus, it cannot only reduce the consumption of high- quality fuel for power generation, but also mitigate greenhouse gas emissions.

  9. Conversation Analysis.

    Science.gov (United States)

    Schiffrin, Deborah

    1990-01-01

    Summarizes the current state of research in conversation analysis, referring primarily to six different perspectives that have developed from the philosophy, sociology, anthropology, and linguistics disciplines. These include pragmatics; speech act theory; interactional sociolinguistics; ethnomethodology; ethnography of communication; and…

  10. Conversion Disorder

    Science.gov (United States)

    ... Recent significant stress or emotional trauma Being female — women are much more likely to develop conversion disorder Having a mental health condition, such as mood or anxiety disorders, dissociative disorder or certain personality disorders Having ...

  11. Studies of the fate of sulfur trioxide in coal-fired utility boilers based on modified selected condensation methods.

    Science.gov (United States)

    Cao, Yan; Zhou, Hongcang; Jiang, Wu; Chen, Chien-Wei; Pan, Wei-Ping

    2010-05-01

    The formation of sulfur trioxide (SO(3)) in coal-fired utility boilers can have negative effects on boiler performance and operation, such as fouling and corrosion of equipment, efficiency loss in the air preheater (APH), increase in stack opacity, and the formation of PM(2.5). Sulfur trioxide can also compete with mercury when bonding with injected activated carbons. Tests in a lab-scale reactor confirmed there are major interferences between fly ash and SO(3) during SO(3) sampling. A modified SO(3) procedure to maximize the elimination of measurement biases, based on the inertial-filter-sampling and the selective-condensation-collecting of SO(3), was applied in SO(3) tests in three full-scale utility boilers. For the two units burning bituminous coal, SO(3) levels starting at 20 to 25 ppmv at the inlet to the selective catalytic reduction (SCR), increased slightly across the SCR, owing to catalytic conversion of SO(2) to SO(3,) and then declined in other air pollutant control device (APCD) modules downstream to approximately 5 ppmv and 15 ppmv at the two sites, respectively. In the unit burning sub-bituminous coal, the much lower initial concentration of SO(3) estimated to be approximately 1.5 ppmv at the inlet to the SCR was reduced to about 0.8 ppmv across the SCR and to about 0.3 ppmv at the exit of the wet flue gas desulfurization (WFGD). The SO(3) removal efficiency across the WFGD scrubbers at the three sites was generally 35% or less. Reductions in SO(3) across either the APH or the dry electrostatic precipitator (ESP) in units burning high-sulfur bituminous coal were attributed to operating temperatures being below the dew point of SO(3).

  12. Impacts of halogen additions on mercury oxidation, in a slipstream selective catalyst reduction (SCR), reactor when burning sub-bituminous coal.

    Science.gov (United States)

    Cao, Yan; Gao, Zhengyang; Zhu, Jiashun; Wang, Quanhai; Huang, Yaji; Chiu, Chengchung; Parker, Bruce; Chu, Paul; Pant, Wei-Ping

    2008-01-01

    This paper presents a comparison of impacts of halogen species on the elemental mercury (Hg(0)) oxidation in a real coal-derived flue gas atmosphere. It is reported there is a higher percentage of Hg(0) in the flue gas when burning sub-bituminous coal (herein Powder River Basin (PRB) coal) and lignite, even with the use of selective catalytic reduction (SCR). The higher Hg(0)concentration in the flue gas makes it difficult to use the wet-FGD process for the mercury emission control in coal-fired utility boilers. Investigation of enhanced Hg(0) oxidation by addition of hydrogen halogens (HF, HCl, HBr, and HI) was conducted in a slipstream reactor with and without SCR catalysts when burning PRB coal. Two commercial SCR catalysts were evaluated. SCR catalyst no. 1 showed higher efficiencies of both NO reduction and Hg(0) oxidation than those of SCR catalyst no. 2. NH3 addition seemed to inhibit the Hg(0) oxidation, which indicated competitive processes between NH3 reduction and Hg(0) oxidation on the surface of SCR catalysts. The hydrogen halogens, in the order of impact on Hg(0) oxidation, were HBr, HI, and HCl or HF. Addition of HBr at approximately 3 ppm could achieve 80% Hg(0) oxidation. Addition of HI at approximately 5 ppm could achieve 40% Hg(0) oxidation. In comparison to the empty reactor, 40% Hg(0) oxidation could be achieved when HCl addition was up to 300 ppm. The enhanced Hg(0) oxidation by addition of HBr and HI seemed not to be correlated to the catalytic effects by both evaluated SCR catalysts. The effectiveness of conversion of hydrogen halogens to halogen molecules or interhalogens seemed to be attributed to their impacts on Hg(0) oxidation.

  13. Strategic conversation

    Directory of Open Access Journals (Sweden)

    Nicholas Asher

    2013-08-01

    Full Text Available Models of conversation that rely on a strong notion of cooperation don’t apply to strategic conversation — that is, to conversation where the agents’ motives don’t align, such as courtroom cross examination and political debate. We provide a game-theoretic framework that provides an analysis of both cooperative and strategic conversation. Our analysis features a new notion of safety that applies to implicatures: an implicature is safe when it can be reliably treated as a matter of public record. We explore the safety of implicatures within cooperative and non cooperative settings. We then provide a symbolic model enabling us (i to prove a correspondence result between a characterisation of conversation in terms of an alignment of players’ preferences and one where Gricean principles of cooperative conversation like Sincerity hold, and (ii to show when an implicature is safe and when it is not. http://dx.doi.org/10.3765/sp.6.2 BibTeX info

  14. Conversion of the compensation measures for the utilization of a FFH area of the brown coal open mining Cottbus North; Umsetzung der Kompensationsmassnahmen fuer die Inanspruchnahme eines FFH-Gebietes durch den Braunkohletagebau Cottbus-Nord

    Energy Technology Data Exchange (ETDEWEB)

    Gerstgraser, Christoph [gerstgraser - Ingenieurbuero fuer Renaturierung, Cottbus (Germany); Arnold, Ingolf; Dingethal, Heidemarie [Vattenfall Europe Mining AG, Cottbus (Germany)

    2008-08-15

    Since the year 1981, the open mining Cottbus-North (Brandenburg, Federal Republic of Germany) produces brown coal. Presently, 5 million tons of brown coal are produced. This brown coal is used in the power generation at the coal-fired power station Jaenschwalde. Within this area of mining there is the pond's group Lakoma. This pond's group consisted of 22 ponds with a total area of 69 ha. These ponds served for breeding of fishes and accommodated protected animal species. In December 2003, the pond's group Lakoma was suggested as a FFH area by the country Brandenburg. With the planning approval procedure for waters, a FFH area was completely eliminated in the approach of an open mining. A licensing procedure came to the result that a removal of these ponds was permissible with consideration of the public interest, if a reconciliation for the plants and animals is carried out. These compensation measures were realized within short time. Thus the open mining Cottbus-North could be continued according to plan.

  15. Component Development to Accelerate Commercial Implementation of Ultra-Low Emissions Catalytic Combustion

    Energy Technology Data Exchange (ETDEWEB)

    McCarty, Jon; Berry, Brian; Lundberg, Kare; Anson, Orris

    2003-03-31

    This final report describes a 2000-2003 program for the development of components and processes to enhance the commercialization of ultra-low emissions catalytic combustion in industrial gas turbines. The range of project tasks includes: development of more durable, lower-cost catalysts and catalytic combustor components; development and design of a catalytic pre-burner and a catalytic pilot burner for gas turbines, and on-site fuel conversion processing for utilization of liquid fuel.

  16. Natural gas conversion process

    Energy Technology Data Exchange (ETDEWEB)

    1992-01-01

    The experimental apparatus was dismantled and transferred to a laboratory space provided by Lawrence Berkeley Laboratory (LBL) which is already equipped with a high-ventilation fume hood. This will enable us to make tests at higher gas flow rates in a safe environment. Three papers presented at the ACS meeting in San Francisco (Symposium on Natural Gas Upgrading II) April 5--10, 1992 show that the goal of direct catalytic conversion of Methane into heavier Hydrocarbons in a reducing atmosphere is actively pursued in three other different laboratories. There are similarities in their general concept with our own approach, but the temperature range of the experiments reported in these recent papers is much lower and this leads to uneconomic conversion rates. This illustrates the advantages of Methane activation by a Hydrogen plasma to reach commercial conversion rates. A preliminary process flow diagram was established for the Integrated Process, which was outlined in the previous Quarterly Report. The flow diagram also includes all the required auxiliary facilities for product separation and recycle of the unconverted feed as well as for the preparation and compression of the Syngas by-product.

  17. From greenhouse gas to feedstock: formation of ammonium carbamate from CO{sub 2} and NH{sub 3} in organic solvents and its catalytic conversion into urea under mild conditions

    Energy Technology Data Exchange (ETDEWEB)

    Barzagli, F.; Mani, F.; Peruzzini, M. [University of Florence, Florence (Italy). Dept. of Chemistry

    2011-07-01

    The capture of carbon dioxide by ammonia in both aqueous and non-aqueous solutions was investigated at atmospheric pressure and 273 K under different operating conditions. The CO{sub 2} capture is fast and efficient ranging between 78 and 99%, depending on both the NH{sub 3} concentration and the solvent nature. The precipitation of solid mixtures of ammonium bicarbonate, ammonium carbonate and ammonium carbamate occurred in ethanol-water solution. Selective precipitation of ammonium carbamate was achieved by reacting gaseous CO{sub 2} and NH{sub 3} in anhydrous ethanol, 1-propanol or N,N-dimethylformamide (DMF) in a flow reactor that operates in continuous. In the second step of the process, the pure ammonium carbamate is used to produce urea with good yield (up to 54% on carbamate basis) at 393-413 K in the presence of inexpensive Cu(II) and Zn(II) catalysts. The yield of urea depends on several factors including the catalyst, the reaction temperature and the reaction time. Identification and quantification of urea in the reaction mixtures was obtained by analysis of its {sup 13}C NMR spectrum. A preliminary mechanistic interpretation of the catalytic reaction is also briefly presented and commented.

  18. Direct Conversion of Energy

    Energy Technology Data Exchange (ETDEWEB)

    Corliss, William R

    1964-01-01

    Topics include: direct versus dynamic energy conversion; laws governing energy conversion; thermoelectricity; thermionic conversion; magnetohydrodynamic conversion; chemical batteries; the fuel cell; solar cells; nuclear batteries; and advanced concepts including ferroelectric conversion and thermomagnetic conversion.

  19. Study on Introduction of Frequency Conversion Control Mode for Motor-driven Feed Pump for 330 MW Coal-fired Boiler%330 MW级燃煤机组锅炉电动给水泵变频改造控制方式变更应用研究

    Institute of Scientific and Technical Information of China (English)

    黄文婧

    2014-01-01

    Energy saving is the most important topic in power generation works of coal-fired power plants now, how-ever, the production of subcritical coal-fired units in China still accounts for a large proportion in total power genera-tion at present. As the dominated subcritical coal-fired units in China, the 330MW units usually adopts 3 sets of mo-tor-driven constant speed feed pumps with single capacity of 70%. The boiler feedwater flows under various condi-tions are regulated through changing electric pump output by fluid coupling control, which unavoidably produces power loss and fluid coupling mechanical loss in electric pump in case of medium load or low load. With the develop-ment of frequency conversion technology, the introduction of the technology in boiler motor-driven feed pump can ef-fectively reduce the feed pump station-service power consumption rate and the unit coal consumption, and produce enormous economic benefits. The paper makes a study on the frequency conversion control mode for boiler mo-tor-driven feed pump based on the practical application.%∶节能降耗工作是目前燃煤发电站各项工作的重中之重,而目前国内亚临界燃煤机组在总发电量上仍占很大比重。330 MW级别机组作为目前国内主流的亚临界燃煤机组,大多采用3台70%容量定速锅炉电动给水泵,通过采取液偶控制方式改变电泵出力来调节各种工况下的锅炉给水流量。从而不可避免地存在中低负荷时电泵的电量损失以及液偶机械损失。随着变频技术的发展,将其运用至锅炉电动给水泵之中能有效地降低电动给水泵厂用电率以及机组供电煤耗,产生巨大的经济效益。文章将从实际应用出发对锅炉电动给水泵变频改造控制方式方面进行探讨研究。

  20. Coal technology program. Progress report, May 1977

    Energy Technology Data Exchange (ETDEWEB)

    None

    1977-07-01

    Two successful operability tests with sustained operation of the bench-scale hydrocarbonizer were achieved with Illinois No. 6 coal diluted with char. Several activities in the area of nondestructive testing of coatings are reviewed. Failure analysis activities included examination of several components from the solvent refined coal plants at Wilsonville, Alabama, and Tacoma, Washington. In the gas-fired potassium boiler project, all of the design work were completed except for several of the instrument and control drawings. In the design studies of a coal-fired alkali metal vapor topping cycle, the first phase of a cycle analysis and the design and analysis of a metal vapor turbine were completed. A report entitled ''Critical Component Test Facility--Advance Planning for Test Modules'' presents the planning study for the conceptual design of component test modules on a nonsite-specific basis. Engineering studies, project evaluation and process and program analysis of coal conversion processes were continued. A report on the landfill storage of solid wastes from coal conversion is being finalized. In the coal-fueled MIUS project, a series of successful tests of the coal feeding system and a report on the analysis of 500-hr fire-side corrosion tests in a fluidized bed combustor were completed.

  1. Effectiveness factors for hydroprocessing of coal and coal liquids

    Energy Technology Data Exchange (ETDEWEB)

    Massoth, F.E.; Seader, J.D.

    1990-06-28

    The aim of this project is to develop a methodology to predict, from a knowledge of feed and catalyst properties, effectiveness factors for catalytic hydroprocessing of coal and coal liquids. The research entails a study of hydrodenitrogenation of model compounds and coal-derived liquids using three NiMo/alumina catalysts of different pore size to develop, for restrictive diffusion. During this quarter equilibrium adsorption studies of single and binary solutes in cyclohexane solvent on three NiMo catalysts were completed. Three single solutes, 9-phenylanthracene, 9-phenylcarbazole, and 9-phenylacridine; and two binary-solute mixtures (9-PhAn/9-PhC and 9-PhC/9-PhAn) were used for the studies. Mathematical models for sorptive diffusion on single- and binary-solute systems were developed. The previously hydrotreated coal-derived-liquid was subjected to a secondary hydrotreatment to achieve a satisfactory product quality. The oil was thoroughly analyzed. Hydrogenation of two nickel-porphines were carried out in this oil and the kinetics was studied with two catalysts under the process conditions. Reaction rates and restrictive diffusion effects were compared to those obtained in the pure solvents from the previous studies. 6 refs., 6 figs., 4 tabs.

  2. Microwave-induced co-processing of coal and biomass

    OpenAIRE

    2015-01-01

    Pyrolysis is an attractive alternative for the conversion of solid fuels to valuable chemicals and bio-fuels. In order to obtain more H2 and syngas from pyrolysis of coal and biomass, microwave has been adopted to enhance the co-pyrolysis of coal and biomass, which has been investigated systematically in this study. Firstly, conventional pyrolysis of coal and biomass was carried out using a vertical tube furnace. Characterizations of pyrolytic gas, liquid and solid products were conducted...

  3. COAL GEOLOGY

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    <正>20091749 Cai Hou’an(College of Energy Geology,China University of Geosciences,Beijing 100083,China);Xu Debin SHRIMP U-Pb Isotope Age of Volcanic Rocks Distributed in the Badaohao Area,Liaoning Province and Its Significance(Coal Geology & Exploration,ISSN1001-1986,CN61-1155/P,36(4),2008,p.17-20,2 illus.,1 table,16 refs.)Key words:coal measures,volcanic rocks,U-Pb dating,LiaoningA set of andesite volcanic rocks distributes in the Badaohao area in Heishan County,Liaoning Province.It’s geological age and stratigraphy sequence relationship between the Lower Cretaceous Badaohao Formation and the volcanic rocks can not make sure till now and is influencing the further prospect for coals.Zircon

  4. Influence of coal blending on mineral transformation at high temperatures

    Institute of Scientific and Technical Information of China (English)

    BAI Jin; LI Wen; LI Chun-zhu; BAI Zong-qing; LI Bao-qing

    2009-01-01

    Transformation of mineral matter is important for coal utilization at high temperatures. This is especially true for blended coal. XRD and FTIR were employed together to study the transformation of mineral matter at high temperature in blended coals. It was found that the concentration of catalytic minerals, namely iron oxides, increases with an increasing ratio of Shenfu coal, which could improve coal gasification. The transformation characteristics of the minerals in blended coals are not exactly predictable from the blend ratio. This was proved by comparing the iron oxide content to the blending ratio. The results from FTIR are comparable with those from XRD. FTIR is an effective method for examining variation in mineral matter.

  5. Behavior of shungite carbon in reactions simulating thermal transformations of coal

    Energy Technology Data Exchange (ETDEWEB)

    Grigor' eva, E.N.; Rozhkova, N.N. [Russian Academy of Science, Moscow (Russian Federation)

    2000-07-01

    The catalytic activity of shungite carbon in reactions of model compounds (tetralin and benzyl phenyl ether) simulating thermolysis of coal was studied. The orders, rate constants, and activation energies of reactions were determined.

  6. Kinetics and mechanisms of hydroliquefaction and hydrogasification of lignite. [Cellulose, wood, manure, municipal waste, coal of various ranks, fuel oil and natural gas

    Energy Technology Data Exchange (ETDEWEB)

    Weiss, A.H.; Kranich, W.L.; Geureuz, K.

    1981-01-01

    A high pressure, continuous, stirred-tank reactor system has been constructed for the study of the catalytic liquefaction of North Dakota lignite slurried in anthracene oil. The conversion of lignite using a cobalt-molybdenum on alumina catalyst and the distribution of products as preasphaltenes, asphaltenes, oils and gases has been studied at the following conditions: temperature, 375 to 440/sup 0/C; pressure, 1000 to 1600 psig; agitator speed, 800 to 1500 rpm; catalyst concentration, 0 to 10% (based on lignite); initial lignite concentration, 5 to 30%; and space time, 16 to 52 minutes. At reactor pressures above 1500 psig and agitator speeds above 1000 rpm, reaction rate was essentially independent of pressure. At catalyst concentrations above 1% (based on lignite), the conversion of lignite was essentially independent of catalyst concentration. Experiments were conducted above these limits to find the effect on lignite conversion rate, of initial lignite concentration, and space time, or degree of conversion. The results at constant temperature were correlated by an equation which is given in the report. The relationship between the rate constant, K, and temperature, and between the maximum conversion and temperature was established. The effect of reaction conditions on the distribution of products was studied. In the presence of catalyst, the oil yield was increased, even under conditions where the catalyst did not affect overall lignite conversion. Under the most favorable conditions the oil yield was a little better than that obtained by Cronauer in the uncatalyzed hydroliquefaction of subbituminous coal at similar temperature and pressure.

  7. Investigation on the catalytic effects of AAEM during steam gasification and the resultant char reactivity in oxygen using Shengli lignite at different forms

    Institute of Scientific and Technical Information of China (English)

    Jianxin Mi; Ningbo Wang; Mingfeng Wang; Pengju Huo; Dan Liu

    2015-01-01

    The purpose of this study is to investigate the catalytic effects of alkali and alkaline earth metallic species (AAEM) on char conversion during the gasification in steam and the changes in ex-situ char reactivity in oxygen after the gasification in steam using different forms (i.e. H-form, Na-form) of Shengli brown coal. The surface area, AAEM concentration and carbon crystallite of chars were obtained to understand the change in char reactivity. It was found that not only Na concentration and carbon structure were the main factors governing the char reactivity in the atmosphere of steam and oxygen, but also they interacted each other. The presence of Na could facilitate the formation of disordering carbon structure in char, and the amorphous carbon structure would in turn affect the distribution of Na and thus its catalytic performance. The surface area and pore volume had very little relationship with the char’s reactivity. Addi-tionally, the morphology of chars from different forms of coals were observed using scanning electron microscope (SEM).

  8. Research on co-liquefaction of highly volatile coal and waste polymer

    Institute of Scientific and Technical Information of China (English)

    宋书宇; 赵鸣

    2002-01-01

    In the paper, the reaction pattern and technological requirement of the co-processing of coal with waste polymer are studied in a 50 ml reactor. The results showed that adding waste polymers during the liquefaction of coal could effectively improve coal conversion, increase oil yield, reduce the cost of hydrogen, and require less strict reaction conditions.

  9. NOVEL SLURRY PHASE DIESEL CATALYSTS FOR COAL-DERIVED SYNGAS

    Energy Technology Data Exchange (ETDEWEB)

    Dr. Dragomir B. Bukur; Dr. Ketil Hanssen; Alec Klinghoffer; Dr. Lech Nowicki; Patricia O' Dowd; Dr. Hien Pham; Jian Xu

    2001-01-07

    This report describes research conducted to support the DOE program in novel slurry phase catalysts for converting coal-derived synthesis gas to diesel fuels. The primary objective of this research program is to develop attrition resistant catalysts that exhibit high activities for conversion of coal-derived syngas.

  10. Unexpectedly high uptake of palladium by bituminous coals

    Energy Technology Data Exchange (ETDEWEB)

    Lakatos, J. [Research Lab. for Mining Chemistry, Hungarian Academy of Sciences, Miskolc-Egyetemvaros (Hungary); Brown, S.D.; Snape, C.E. [Univ. of Strathclyde, Dept. of Pure and Applied Chemistry, Glasgow (United Kingdom)

    1997-12-31

    The uptake of palladium as a conversion catalyst onto coals of different rank was investigated. Palladium fixation occurs by a different mode to that for alkaline earth and first row transition metals. Therefore, the dispersion of relatively high concentration of palladium by an ion sorption process is even possible for bituminous coals. (orig.)

  11. Catalytic conversion of carbon dioxide into dimethyl carbonate using reduced copper-cerium oxide catalysts as low as 353 K and 1.3 MPa and the reaction mechanism

    Directory of Open Access Journals (Sweden)

    Seiki eWada

    2013-06-01

    Full Text Available Synthesis of dimethyl carbonate (DMC from CO2 and methanol under milder reaction conditions was performed using reduced cerium oxide catalysts and reduced copper-promoted Ce oxide catalysts. Although the conversion of methanol was low (0.005–0.11% for 2 h of reaction, DMC was synthesized as low as 353 K and at total pressure of as low as 1.3 MPa using reduced Cu–CeO2 catalyst (0.5 wt% of Cu. The apparent activation energy was 120 kJ mol–1 and the DMC synthesis rates were proportional to the partial pressure of CO2. An optimum amount of Cu addition to CeO2 was 0.1 wt% for DMC synthesis under the conditions at 393 K and total pressure of 1.3 MPa for 2 h (conversion of methanol: 0.15% due to the compromise of two effects of Cu: the activation of H2 during reduction prior to the kinetic tests and the block (cover of the surface active site. The reduction effects in H2 were monitored through the reduction of Ce4+ sites to Ce3+ based on the shoulder peak intensity at 5727 eV in the Ce L3-edge X-ray absorption near-edge structure (XANES. The Ce3+ content was 10% for reduced CeO2 catalyst whereas it increased to 15% for reduced Cu–CeO2 catalyst (0.5wt% of Cu. Moreover, the content of reduced Ce3+ sites (10% associated with the surface O vacancy (defect sites decreased to 5% under CO2 at 290 K for reduced Cu–CeO2 catalyst (0.1wt% of Cu. The adsorption step of CO2 on the defect sites might be the key step in DMC synthesis and thus the DMC synthesis rate dependence on the partial pressure of CO2 was proportional. Subsequent H atom subtraction steps from methanol at the neighboring surface Lewis base sites should combine two methoxy species to the adsorbed CO2 to form DMC, water, and restore the surface O vacancy.

  12. Fischer-Tropsch Synthesis: Influence of CO Conversion on Selectivities H2/CO Usage Ratios and Catalyst Stability for a 0.27 percent Ru 25 percent Co/Al2O3 using a Slurry Phase Reactor

    Energy Technology Data Exchange (ETDEWEB)

    W Ma; G Jacobs; Y Ji; T Bhatelia; D Bukur; S Khalid; B Davis

    2011-12-31

    The effect of CO conversion on hydrocarbon selectivities (i.e., CH{sub 4}, C{sub 5+}, olefin and paraffin), H{sub 2}/CO usage ratios, CO{sub 2} selectivity, and catalyst stability over a wide range of CO conversion (12-94%) on 0.27%Ru-25%Co/Al{sub 2}O{sub 3} catalyst was studied under the conditions of 220 C, 1.5 MPa, H{sub 2}/CO feed ratio of 2.1 and gas space velocities of 0.3-15 NL/g-cat/h in a 1-L continuously stirred tank reactor (CSTR). Catalyst samples were withdrawn from the CSTR at different CO conversion levels, and Co phases (Co, CoO) in the slurry samples were characterized by XANES, and in the case of the fresh catalysts, EXAFS as well. Ru was responsible for increasing the extent of Co reduction, thus boosting the active site density. At 1%Ru loading, EXAFS indicates that coordination of Ru at the atomic level was virtually solely with Co. It was found that the selectivities to CH{sub 4}, C{sub 5+}, and CO{sub 2} on the Co catalyst are functions of CO conversion. At high CO conversions, i.e. above 80%, CH{sub 4} selectivity experienced a change in the trend, and began to increase, and CO{sub 2} selectivity experienced a rapid increase. H{sub 2}/CO usage ratio and olefin content were found to decrease with increasing CO conversion in the range of 12-94%. The observed results are consistent with water reoxidation of Co during FTS at high conversion. XANES spectroscopy of used catalyst samples displayed spectra consistent with the presence of more CoO at higher CO conversion levels.

  13. Nitrogen release during coal combustion

    Energy Technology Data Exchange (ETDEWEB)

    Baxter, L.L.; Mitchell, R.E.; Fletcher, T.H.; Hurt, R.H.

    1995-02-01

    Experiments in entrained flow reactors at combustion temperatures are performed to resolve the rank dependence of nitrogen release on an elemental basis for a suite of 15 U.S. coals ranging from lignite to low-volatile bituminous. Data were obtained as a function of particle conversion, with overall mass loss up to 99% on a dry, ash-free basis. Nitrogen release rates are presented relative to both carbon loss and overall mass loss. During devolatilization, fractional nitrogen release from low-rank coals is much slower than fractional mass release and noticeably slower than fractional carbon release. As coal rank increases, fractional nitrogen release rate relative to that of carbon and mass increases, with fractional nitrogen release rates exceeding fractional mass and fractional carbon release rates during devolatilization for high-rank (low-volatile bituminous) coals. At the onset of combustion, nitrogen release rates increase significantly. For all coals investigated, cumulative fractional nitrogen loss rates relative to those of mass and carbon passes through a maximum during the earliest stages of oxidation. The mechanism for generating this maximum is postulated to involve nascent thermal rupture of nitrogen-containing compounds and possible preferential oxidation of nitrogen sites. During later stages of oxidation, the cumulative fractional loss of nitrogen approaches that of carbon for all coals. Changes in the relative release rates of nitrogen compared to those of both overall mass and carbon during all stages of combustion are attributed to a combination of the chemical structure of coals, temperature histories during combustion, and char chemistry.

  14. Conversational Telugu.

    Science.gov (United States)

    Beinstein, Judith; And Others

    The purpose of this text is to develop elementary conversational skills in Telugu. The language materials consist of four types of language learning activities. The first, and most predominant, is the unit microwave cycle. These cycles divide the learning process into two basic phases, the first of which involves mimicry, memorization, and…

  15. Oxidation of elemental mercury by modified spent TiO2-based SCR-DeNOx catalysts in simulated coal-fired flue gas.

    Science.gov (United States)

    Zhao, Lingkui; Li, Caiting; Zhang, Xunan; Zeng, Guangming; Zhang, Jie; Xie, Yin'e

    2016-01-01

    In order to reduce the costs, the recycle of spent TiO2-based SCR-DeNOx catalysts were employed as a potential catalytic support material for elemental mercury (Hg(0)) oxidation in simulated coal-fired flue gas. The catalytic mechanism for simultaneous removal of Hg(0) and NO was also investigated. The catalysts were characterized by Brunauer-Emmett-Teller (BET), scanning electron microscope (SEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) method. Results indicated that spent TiO2-based SCR-DeNOx catalyst supported Ce-Mn mixed oxides catalyst (CeMn/SCR1) was highly active for Hg(0) oxidation at low temperatures. The Ce1.00Mn/SCR1 performed the best catalytic activities, and approximately 92.80% mercury oxidation efficiency was obtained at 150 °C. The inhibition effect of NH3 on Hg(0) oxidation was confirmed in that NH3 consumed the surface oxygen. Moreover, H2O inhibited Hg(0) oxidation while SO2 had a promotional effect with the aid of O2. The XPS results illustrated that the surface oxygen was responsible for Hg(0) oxidation and NO conversion. Besides, the Hg(0) oxidation and NO conversion were thought to be aided by synergistic effect between the manganese and cerium oxides.

  16. Reactivity of organic compounds in catalytic synthesis

    Energy Technology Data Exchange (ETDEWEB)

    Minachev, Kh.M.; Bragin, O.V.

    1978-01-01

    A comprehensive review of 1976 Soviet research on catalysis delivered to the 1977 annual session of the USSR Academy of Science Council on Catalysis (Baku 6/16-20/77) covers hydrocarbon reactions, including hydrogenation and hydrogenolysis, dehydrogenation, olefin dimerization and disproportionation, and cyclization and dehydrocyclization (e.g., piperylene cyclization and ethylene cyclotrimerization); catalytic and physicochemical properties of zeolites, including cracking, dehydrogenation, and hydroisomerization catalytic syntheses and conversion of heterocyclic and functional hydrocarbon derivatives, including partial and total oxidation (e.g., of o-xylene to phthalic anhydride); syntheses of thiophenes from alkanes and hydrogen sulfide over certain dehydrogenation catalysts; catalytic syntheses involving carbon oxides ( e.g., the development of a new heterogeneous catalyst for hydroformylation of olefins), and of Co-MgO zeolitic catalysts for synthesis of aliphatic hydrocarbons from carbon dioxide and hydrogen, and fabrication of high-viscosity lubricating oils over bifunctional aluminosilicate catalysts.

  17. Flash pyrolysis of coal-solvent slurry prepared from the oxidized coal and the coal dissolved in solvent; Ichibu yokaishita sanka kaishitsutan slurry no jinsoku netsubunkai

    Energy Technology Data Exchange (ETDEWEB)

    Maki, T.; Mae, K.; Okutsu, H.; Miura, K. [Kyushu University, Fukuoka (Japan). Faculty of Engineering

    1996-10-28

    In order to develop a high-efficiency coal pyrolysis method, flash pyrolysis was experimented on slurry prepared by using liquid-phase oxidation reformed coal and a methanol-based solvent mixture. Australian Morwell coal was used for the experiment. The oxidized coal, into which carboxyl groups have been introduced, has the condensation structure relaxed largely, and becomes highly fluid slurry by means of the solvent. Char production can be suppressed by making the oxidation-pretreated coal into slurry, resulting in drastically improved pyrolytic conversion. The slurry was divided into dissolved solution, dried substance, extracted residue, and residual slurry, which were pyrolized independently. The dissolved solution showed very high conversion. Improvement in the conversion is contributed by separating the dissolved substances (coal macromolecules) at molecular levels, coagulating the molecules, suppressing cross-link formation, and reducing molecular weight of the dissolved substances. Oxidized coal can be dissolved to 80% or higher by using several kinds of mixed solvents. As a result of the dissolution, a possibility was suggested on pyrolysis which is easy in handling and high in conversion. 7 refs., 6 figs., 2 tabs.

  18. Coal industry annual 1997

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1998-12-01

    Coal Industry Annual 1997 provides comprehensive information about US coal production, number of mines, prices, productivity, employment, productive capacity, and recoverable reserves. US Coal production for 1997 and previous years is based on the annual survey EIA-7A, Coal Production Report. This report presents data on coal consumption, coal distribution, coal stocks, coal prices, and coal quality for Congress, Federal and State agencies, the coal industry, and the general public. Appendix A contains a compilation of coal statistics for the major coal-producing States. This report includes a national total coal consumption for nonutility power producers that are not in the manufacturing, agriculture, mining, construction, or commercial sectors. 14 figs., 145 tabs.

  19. Coal industry annual 1996

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1997-11-01

    This report presents data on coal consumption, coal distribution, coal stocks, coal prices, and coal quality, and emissions for Congress, Federal and State agencies, the coal industry, and the general public. Appendix A contains a compilation of coal statistics for the major coal-producing States.This report does not include coal consumption data for nonutility power producers that are not in the manufacturing, agriculture, mining, construction, or commercial sectors. Consumption for nonutility power producers not included in this report is estimated to be 24 million short tons for 1996. 14 figs., 145 tabs.

  20. Coal Industry Annual 1995

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-10-01

    This report presents data on coal consumption, coal distribution, coal stocks, coal prices, coal quality, and emissions for Congress, Federal and State agencies, the coal industry, and the general public. Appendix A contains a compilation of coal statistics for the major coal-producing States. This report does not include coal consumption data for nonutility power producers that are not in the manufacturing, agriculture, mining, construction, or commercial sectors. Consumption for nonutility power producers not included in this report is estimated to be 21 million short tons for 1995.