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" Methane homologation by the two-step cycle on Co catalysts "
J. S. Soltan Mohammad Zadeh
K. J. Smith
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Latin Dissertation
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English
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| Record Number
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1113428
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TLpq304492429
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| Main Entry
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J. S. Soltan Mohammad Zadeh
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K. J. Smith
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| Title & Author
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Methane homologation by the two-step cycle on Co catalysts\ J. S. Soltan Mohammad ZadehK. J. Smith
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| College
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The University of British Columbia (Canada)
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| Date
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1998
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| student score
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1998
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| Degree
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Ph.D.
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| Page No
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208
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| Abstract
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Conversion of natural gas to liquid hydrocarbons upgrades a low density fuel to a valuable source of chemicals and liquid fuel. To eliminate the expensive intermediate step of methane-steam reforming in the commercial Fischer-Tropsch, methanol to gasoline and Shell middle distillate synthesis processes, a direct method of CH4 conversion to higher hydrocarbons is very desirable. In direct conversion of CH4 to higher hydrocarbons in the presence of O2 (e.g. oxidative coupling and partial oxidation), deep oxidation of CH4 to CO and CO2 is a major drawback. In the two-step homologation of CH4 in the absence of O2, CH4 is first activated on a reduced transition metal catalyst at high temperature (e.g. 450C) to produce H2 and carbon species on the catalyst. The carbon species are then hydrogenated in the second step at a lower temperature (e.g. 100C) to produce CH4 and higher hydrocarbons. In the present study of the two-step homologation of CH4, SiO2 supported Co catalysts were prepared by incipient impregnation. The catalysts were characterized by BET surface area and pore volume measurement, powder X-ray diffraction, temperature programmed reduction, H2 chemisorption and Co re-oxidation. Carbon species deposited in the activation step were recovered by isothermal hydrogenation at 100C, temperature programmed surface reaction and temperature programmed oxidation to account for the reactivity of different carbon species. The effect of catalyst loading, activation time, activation temperature, carbon aging, reaction cycle and isothermal medium on both the CH4 activation step and the isothermal hydrogenation to C{2+} hydrocarbons, were studied. Based on the findings from deposition of more than a nominal monolayer carbon coverage on the supported metal, a semi-empirical kinetic model for the activation of CH4 on Co-SiO2 catalysts was developed. In the kinetic model, gas phase CH4 is first activated on Co to produce adsorbed H and CH3 species. Migration of some of the CH3 species from the metal to the support liberates Co sites for further reaction. H2 is generated by further dehydrogenation of CH3 species on the metal and support, and desorption of adsorbed H. The kinetic model and rate constants of different steps were used to interpret the effect of changes in operating conditions on the rate of different steps of the CH4 activation reaction. Metal-support interactions in the Co-SiO2 system play an important role in CH4 activation and in determining the activity of carbon species. With more than a nominal monolayer coverage of metal by carbon, a considerable amount of inactive carbon, which can only be removed by high temperature oxidation, is produced on the support. Hydrogen content and age of the carbon species were among the important factors affecting C{2+} production in isothermal hydrogenation. It was shown that C-C bond formation occurs to a great extent before the isothermal hydrogenation step.
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Applied sciences
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carbon
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Chemical engineering
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cobalt
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