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dc.contributor.authorBhatelia, Tejas
dc.contributor.authorMa, W.
dc.contributor.authorDavis, B.
dc.contributor.authorJacobs, G.
dc.contributor.authorDrabukur, G.
dc.date.accessioned2018-02-01T05:21:37Z
dc.date.available2018-02-01T05:21:37Z
dc.date.created2018-02-01T04:49:10Z
dc.date.issued2011
dc.identifier.citationBhatelia, T. and Ma, W. and Davis, B. and Jacobs, G. and Drabukur, G. 2011. Kinetics of the fischer-tropsch reaction over a Ru-promoted Co/Al2o3catalyst, pp. 707-712.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/62086
dc.identifier.doi10.3303/CET1125118
dc.description.abstract

The kinetics of the Fischer Tropsch (FT) synthesis reaction over 0.27 % Ru 25 % Co/Al 2 o 3 catalyst was studied in a 1L stirred tank slurry reactor (STSR). Experiments were conducted at reactor pressures of 1.4 MPa and 2.4 MPa, temperatures of 205°C and 220°C, H 2 /CO feed ratios of 1.4 and 2.1 and gas space velocities ranging from 2 to 15 NL/g-cath. Langmuir-Hinshelwood-Hougen-Watson (LHHW) type rate equations were derived on the basis of a set of reactions originating from carbide and enolic pathways for hydrocarbon formation. Derived rate equations were fitted to the corrected experimental rate using Levenberg-Marquardt method to obtain model parameters. Physical and statistical tests were used to discriminate between rival models. It was found that a model based on hydrogen-assisted dissociative adsorption of CO followed by hydrogenation of dissociatively adsorbed CO provides the best fit to the data. Copyright © 2011, AIDIC Servizi S.r.l.

dc.titleKinetics of the fischer-tropsch reaction over a Ru-promoted Co/Al2o3catalyst
dc.typeConference Paper
dcterms.source.volume25
dcterms.source.startPage707
dcterms.source.endPage712
dcterms.source.issn2283-9216
dcterms.source.titleChemical Engineering Transactions
dcterms.source.seriesChemical Engineering Transactions
curtin.departmentWASM: Minerals, Energy and Chemical Engineering (WASM-MECE)
curtin.accessStatusFulltext not available


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