Etherification of aldehydes, alcohols and their mixtures on Pd/SiO2 catalysts

被引:16
|
作者
Pham, Trung T. [1 ]
Crossley, Steven. P. [1 ]
Sooknoi, Tawan [1 ]
Lobban, Lance L. [1 ]
Resasco, Daniel E. [1 ]
Mallinson, Richard G. [1 ]
机构
[1] Univ Oklahoma, Sch Chem Biol & Mat Engn, Norman, OK 73019 USA
基金
美国国家科学基金会;
关键词
Etherification; Hydrogenation; Decarbonylation; Aldehyde; Alcohol; DECOMPOSITION PATHWAYS; BIMETALLIC CATALYSTS; ALDOL-CONDENSATION; SURFACE-REACTION; METAL-CATALYSTS; ADSORPTION; HYDROGENATION; PALLADIUM; ACETONE; KETONES;
D O I
10.1016/j.apcata.2010.03.014
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
Dialkyl ethers have been selectively produced from etherification of aldehydes and alcohols on supported Pd catalysts. A yield of 79% ether with a selectivity of 90% was observed when feeding 2-methylpentanal with 2-methylpentanol at a molar ratio 1:1 at 125 degrees C. Cross etherification of n-butanol with 2-methylpentanal shows a much higher rate than that observed when the alcohol or aldehyde is fed alone. This enhanced activity is in line with the catalyst requirement for large ensembles that allow surface alkoxide species next to eta(2) adsorbed aldehydes. Etherification when only aldehyde or alcohol is fed arises predominantly due to aldehyde-alcohol inter-conversion to produce the necessary co-reactant. The ether yield at the same reaction conditions decreases with metal loading in the order 16 > 10 > 3 wt.% Pd. Increasing reduction temperature also increases ether yield. It is apparent that etherification is highly sensitive to metal particle morphology, consistent with needing ensembles that accommodate the two adjacent adsorption sites. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:135 / 140
页数:6
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