CATALYTIC CONVERSION OF ALCOHOLS .13. ALKENE SELECTIVITY WITH TIO2 CATALYSTS

被引:12
作者
COLLINS, DJ
WATTERS, JC
DAVIS, BH
机构
[1] POTOMAC STATE COLL,KEYSER,WV 26726
[2] UNIV LOUISVILLE,DEPT CHEM ENGN,LOUISVILLE,KY 40208
来源
INDUSTRIAL & ENGINEERING CHEMISTRY PRODUCT RESEARCH AND DEVELOPMENT | 1979年 / 18卷 / 03期
关键词
D O I
10.1021/i360071a009
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Anatase is a very selective dehydration catalyst and the alkenes formed from 2-ols resemble those formed with an alumina catalyst. Rutile is not a selective dehydration catalyst; the alkene selectivity depends on pretreatment and it is more selective for 1-alkene formation from 2-ols than anatase. With anatase the more rapid conversion of cis-2-methylcyclohexanol isomer and the different alkene composition from the two alcohol isomers are consistent with a contribution of an anti elimination mechanism. For the conversion of alcohols with group 4A metal oxide catalysts, anatase and hafnia resemble each other but differ markedly from zirconia and thoria. © 1979, American Chemical Society. All rights reserved.
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页码:202 / 205
页数:4
相关论文
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