Perspectives on the kinetics of diol oxidation over supported platinum catalysts in aqueous solution

被引:34
|
作者
Ide, Matthew S. [1 ]
Davis, Robert J. [1 ]
机构
[1] Univ Virginia, Dept Chem Engn, Charlottesville, VA 22904 USA
基金
美国国家科学基金会;
关键词
Alcohol oxidation; Diol; Polyol; Aldehyde; Diacid; Kinetics; Mechanism; Platinum; Heterogeneous catalysis; Kinetic isotope effect; LIQUID-PHASE OXIDATION; SELECTIVE OXIDATION; ALCOHOL OXIDATION; 3-ELECTRON OXIDATIONS; CARBON-MONOXIDE; PARTICLE-SIZE; OXYGEN; GOLD; ETHANOL; ACID;
D O I
10.1016/j.jcat.2013.05.017
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The catalytic oxidation of a variety of terminal alcohols was performed over Pt/C with 10 bar dioxygen at 343 K in aqueous solvent at low pH. The influences of Pt particle size, carbon support, alcohol structure, and start-up conditions were explored. Although the turnover frequency was not affected by particle size or the carbon support, the structure of the alcohols affected their initial rate of conversion. Both the rate of oxidation of alpha,omega-diols and selectivity of the diols to the diacids increased with increasing carbon chain length. The rate of 1,6-hexanediol oxidation was independent of dioxygen pressure and the order of reaction with respect to diol concentration depended on the start-up conditions. A kinetic model involving two types of metal sites was proposed to account for the experimental observations. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:50 / 59
页数:10
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