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Isobutane Dehydrogenation over Metal (Fe, Co, and Ni) Oxide and Sulfide Catalysts: Reactivity and Reaction Mechanism
Author(s) -
Wang Guowei,
Gao Chuancheng,
Zhu Xiaolin,
Sun Yanan,
Li Chunyi,
Shan Honghong
Publication year - 2014
Publication title -
chemcatchem
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.497
H-Index - 106
eISSN - 1867-3899
pISSN - 1867-3880
DOI - 10.1002/cctc.201402173
Subject(s) - isobutane , dehydrogenation , hydrogenolysis , catalysis , chemistry , sulfidation , sulfide , inorganic chemistry , hydrogen sulfide , oxide , reactivity (psychology) , metal , sulfur , organic chemistry , medicine , alternative medicine , pathology
Silica‐supported metal oxide and sulfide catalysts of Fe, Co, and Ni were evaluated comparatively for the catalytic dehydrogenation of isobutane. The results of the activity test and temperature‐programmed reduction of hydrogen characterization indicate that metal oxides, except Fe 2 O 3 , are easily reduced to metal ensembles, which are extremely active for alkane hydrogenolysis and lead to the formation of a considerable amount of methane and coke. However, the dehydrogenation performance was significantly improved after sulfidation treatment. The introduction of sulfur affects the catalysts in two ways: one is the geometric effect, which dilutes the aggregated metallic species and reduces hydrogenolysis activity, and the other is the electronic effect, which facilitates the desorption of olefin and increases the product selectivity. Moreover, the reaction mechanism is explored by using the proposed model of the interaction between isobutane and sulfide catalysts. Finally, sulfur loss and partial coke deposition are determined to be the main reasons for catalyst deactivation.