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Development of a kinetic model for alcohol synthesis over a cesium-promoted Cu/ZnO catalyst

Journal Article · · Industrial and Engineering Chemistry Research; (United States)
OSTI ID:6084051
;  [1];  [2];  [3]
  1. Zettlemoyer Center for Surface Studies, Dept. of Chemistry, Lehigh Univ., Bethlehem, PA (US)
  2. Alberta Research Council, Coal and Hydrocarbon Processing Div., Devon, Alberta T0C 1E0 (CA)
  3. China Steel Corp., New Material R and D Dept. T6, Hsiao Kang, Kaohsiung 81233 (TW)
This paper reports on a kinetic reaction network developed for the synthesis of oxygenates from synthesis gave over Cs-promoted Cu/ZnO catalysts in a differential reaction regime. The most important carbon- carbon bond forming reactions of the model are linear growth by addition of an oxygenated C{sub 1} intermediate to an alcohol chain that yields linear alcohols and a {beta}-addition aldol condensation type mechanism between an oxygenated C{sub 1} intermediate and an aldehydic C{sub n} intermediate that yields 2-methyl-branched primary alcohols. The most important carbon-oxygen bond forming reaction is a methoxide addition, {eta}{sub 0}, that yields methyl esters. Estimates of the kinetic parameters show that the {beta} addition is faster than linear growth, which results in high selectivities to branched alcohols, i.e., 2-methyl-1- propanol.
OSTI ID:
6084051
Journal Information:
Industrial and Engineering Chemistry Research; (United States), Journal Name: Industrial and Engineering Chemistry Research; (United States) Vol. 30:1; ISSN 0888-5885; ISSN IECRE
Country of Publication:
United States
Language:
English