Reduction of chloroacetone over silica-supported noble metal catalysts

被引:5
|
作者
Mori, T [1 ]
Tomikawa, D [1 ]
Katano, Y [1 ]
Kubo, J [1 ]
Morikawa, Y [1 ]
机构
[1] Tokyo Inst Technol, Chem Resources Lab, Midori Ku, Yokohama, Kanagawa 2268503, Japan
关键词
hydrogenation; hydrogenolysis; hydrodechlorination; chloroacetone; acetone; noble metal catalysts;
D O I
10.1016/j.apcata.2004.02.048
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 reduction of chloroacetone over silica-supported noble metal catalysts yielded the hydrodechlorinated (acetone), the hydrogenated (1-chloro-2-propanol), and the hydrodechlorinated-hydrogenated (2-propanol) products at different selectivities depending on the catalyst used. Pd/SiO2 catalyzed the single-step hydrodechlorination preferentially to give acetone selectively. Pt/SiO2 promoted the hydrogenation into 1-chloro-2-propanol concurrently and the consecutive hydrogenation of acetone into 2-propanol as well. Over Rh/SiO2, acetone was transformed to 1-chloro-2-propanol through the addition of hydrogen chloride. The hydrodechlorination activity of noble metals followed the order of Pd > Pt much greater than Rh > Ru. The high selectivity of Pd/SiO2 toward acetone was not influenced by Pd dispersion. The selectivity Of Pt/SiO2 changed largely with Pt dispersion and the hydrogenation of carbonyl group was promoted preferentially over the catalysts with low Pt dispersion. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:77 / 84
页数:8
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