Coke removal from deactivated Co-Ni steam reforming catalyst using different gasifying agents: An analysis of the gas-solid reaction kinetics
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作者:
Alenazey, F.
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Univ New S Wales, Sch Chem Sci & Engn, Reactor Engn & Technol Grp, Sydney, NSW 2052, AustraliaUniv New S Wales, Sch Chem Sci & Engn, Reactor Engn & Technol Grp, Sydney, NSW 2052, Australia
Alenazey, F.
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Cooper, C. G.
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Univ New S Wales, Sch Chem Sci & Engn, Reactor Engn & Technol Grp, Sydney, NSW 2052, AustraliaUniv New S Wales, Sch Chem Sci & Engn, Reactor Engn & Technol Grp, Sydney, NSW 2052, Australia
Cooper, C. G.
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Dave, C. B.
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Univ New S Wales, Sch Chem Sci & Engn, Reactor Engn & Technol Grp, Sydney, NSW 2052, AustraliaUniv New S Wales, Sch Chem Sci & Engn, Reactor Engn & Technol Grp, Sydney, NSW 2052, Australia
Dave, C. B.
[1
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Elnashaie, S. S. E. H.
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Penn State Univ Harrisburg, Capital Coll, Middletown, PA 17057 USAUniv New S Wales, Sch Chem Sci & Engn, Reactor Engn & Technol Grp, Sydney, NSW 2052, Australia
Elnashaie, S. S. E. H.
[2
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Susu, A. A.
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Univ Lagos, Dept Chem Engn, Lagos, NigeriaUniv New S Wales, Sch Chem Sci & Engn, Reactor Engn & Technol Grp, Sydney, NSW 2052, Australia
Susu, A. A.
[3
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Adesina, A. A.
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Univ New S Wales, Sch Chem Sci & Engn, Reactor Engn & Technol Grp, Sydney, NSW 2052, AustraliaUniv New S Wales, Sch Chem Sci & Engn, Reactor Engn & Technol Grp, Sydney, NSW 2052, Australia
Adesina, A. A.
[1
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[1] Univ New S Wales, Sch Chem Sci & Engn, Reactor Engn & Technol Grp, Sydney, NSW 2052, Australia
[2] Penn State Univ Harrisburg, Capital Coll, Middletown, PA 17057 USA
The reactivity of various gases, namely; O-2, air, CO2, H-2 and N-2, with carbon deposited on alumina-supported Co-Ni catalyst during propane reforming in a fluidized bed reactor at 773-973 K using relatively low feed steam:carbon ratio (0.8-1.5) has been investigated in a thermogravimetric analysis unit. Analysis of the transient solid weight loss revealed that carbon removal mechanism is dependent on the type of gasifying agent. Carbon gasification kinetics using O-2 and air followed the Avrami-Erofeev (A2) model while data for both CO2 and H-2 were captured by the geometrical (contracting area. R2) model. However, carbon gasification with inert N2 proceeded at much slower rate (about 10 times lower than air) and was adequately fitted by the one-dimensional diffusion (D1) model. Specific reaction rates from these phenomenological models were also linearly correlated with the catalyst carbon content with reactivity coefficient of the gasifying agent decreasing in the order, O-2 > air > CO2 > H-2 > N-2. In order to minimize energy consumption during catalyst regeneration, reduce greenhouse gas emissions and reduce catalyst sintering, it would be desirable to employ a mixture of air and CO2 as the carbon gasifying agent to take advantage of the coupled exothermic (air oxidation) and endothermic (reverse Boudouard reaction involving CO2 and carbon) nature taking place during the carbon removal operation. (c) 2008 Elsevier B.V. All rights reserved.
机构:Univ Fed Rio de Janeiro, COPPE, Peq, Nucat, BR-21941 Rio De Janeiro, Brazil
Alberton, Andre L.
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Souza, Mariana M. V. M.
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机构:Univ Fed Rio de Janeiro, COPPE, Peq, Nucat, BR-21941 Rio De Janeiro, Brazil
Souza, Mariana M. V. M.
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Schmal, Martin
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Univ Fed Rio de Janeiro, COPPE, Peq, Nucat, BR-21941 Rio De Janeiro, BrazilUniv Fed Rio de Janeiro, COPPE, Peq, Nucat, BR-21941 Rio De Janeiro, Brazil
机构:
Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, JapanKyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan
机构:Univ Fed Rio de Janeiro, COPPE, Peq, Nucat, BR-21941 Rio De Janeiro, Brazil
Alberton, Andre L.
;
Souza, Mariana M. V. M.
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机构:Univ Fed Rio de Janeiro, COPPE, Peq, Nucat, BR-21941 Rio De Janeiro, Brazil
Souza, Mariana M. V. M.
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Schmal, Martin
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Univ Fed Rio de Janeiro, COPPE, Peq, Nucat, BR-21941 Rio De Janeiro, BrazilUniv Fed Rio de Janeiro, COPPE, Peq, Nucat, BR-21941 Rio De Janeiro, Brazil
机构:
Kyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, JapanKyoto Univ, Grad Sch Engn, Dept Energy & Hydrocarbon Chem, Nishikyo Ku, Kyoto 6158510, Japan