陆安慧

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教授

博士生导师

硕士生导师

主要任职:校长助理

其他任职:精细化工国家重点实验室副主任,辽宁省低碳资源高值化利用重点实验室主任

性别:男

毕业院校:中科院山西煤化所

学位:博士

所在单位:化工学院

学科:工业催化. 化学工艺. 能源化工

办公地点:大连市凌工路2号大连理工大学西部校区化工楼,邮编:116024

联系方式:0411-84986112

电子邮箱:anhuilu@dlut.edu.cn

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Highly Selective Copper Catalyst Supported on Mesoporous Carbon for the Dehydrogenation of Ethanol to Acetaldehyde

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论文类型:期刊论文

发表时间:2015-09-14

发表刊物:CHEMCATCHEM

收录刊物:SCIE、EI、Scopus

卷号:7

期号:18,SI

页面范围:2846-2852

ISSN号:1867-3880

关键字:carbon; copper; dehydrogenation; mesoporous materials; supported catalysts

摘要:The dehydrogenation of ethanol to acetaldehyde is of great importance in synthetic chemistry and the fine chemical industry. In this study, we report that a mesoporous-carbon-supported Cu catalyst exhibited a high reaction rate and excellent product selectivity in ethanol dehydrogenation to acetaldehyde. Under the severe conditions of an ethanol concentration of 15vol% and a gaseous hourly space velocity of 8600h(-1), the Cu-based carbon catalyst maintains a conversion of approximate to 73% and an acetaldehyde selectivity of approximate to 94% at 553K. Meanwhile, a prominent space time yield (225h(-1)) of acetaldehyde is obtained, which is far higher than that (112h(-1)) on the mesoporous-SBA-15-supported Cu catalyst. Ethanol adsorption studies prove that the enrichment of the carbon support for reactants makes a contribution to the high reaction rate. Importantly, kinetic measurements indicate that the scarce surface groups of the mesoporous carbon support minimize the secondary reactions of acetaldehyde, which are generally catalyzed by OH and/or COOH on the surface of the support as exemplified by the mesoporous-SBA-15-supported Cu catalyst. This accounts for the excellent selectivity toward acetaldehyde on the mesoporous-carbon-supported Cu catalyst. Therefore, these surface characteristics of the carbon support show great advantages in this dehydrogenation reaction.