包明

个人信息Personal Information

教授

博士生导师

硕士生导师

性别:男

毕业院校:日本东北大学

学位:博士

所在单位:化工学院盘锦分院

办公地点:精细化工国家重点实验室E504

电子邮箱:mingbao@dlut.edu.cn

扫描关注

论文成果

当前位置: 中文主页 >> 科学研究 >> 论文成果

Selective Hydrogenation of Cinnamaldehyde to Cinnamyl Alcohol over Au Catalysts: Influence of the Oxide-Supports

点击次数:

论文类型:期刊论文

发表时间:2017-01-01

发表刊物:CATALYSIS LETTERS

收录刊物:SCIE、EI

卷号:147

期号:1

页面范围:102-109

ISSN号:1011-372X

关键字:Gold catalysis; Selective hydrogenation; Cinnamaldehyde; Cinnamyl alcohol; Acidity/basicity

摘要:Uniform Au particles with a mean size of 1.9 nm were initially synthesized with polyvinyl alcohol (PVA) as protecting agent, and then deposited on MgO, Al2O3, TiO2, Fe2O3, Co3O4, ZnO and In2O3. After calcinations at 300 A degrees C in air to remove PVA, Au particles were highly dispersed and immobilized on all the supports, displaying narrow diameter distributions and almost identical mean sizes of 2.5-3.2 nm. The Au-oxides catalysts were further used to catalyze selective hydrogenation of cinnamaldehyde (CAL) to cinnamyl alcohol (COL). It was found that the selectivity of COL was tightly related to the acidity/basicity of the Au/oxides catalysts. The catalyst with only acidic sites such as the Au/Al2O3 catalyst gave very low selectivity of COL of 15%. The catalysts with only basic sites such as Au/MgO catalyst displayed medium selectivity of COL of 52%. Interesting, the Au catalysts with both acidic and basic sites such as the Au/In2O3 and Au/ZnO catalyts exhibited the highest selectivity of COL of around 86%. The synergistic cooperation of acidic sites and basic sites should be responsible for preferential adsorption and activation of the C=O group than C=C group in CAL, and then preferential hydrogenation of C=O to COL.
   [GRAPHICS]