李文翠

个人信息Personal Information

教授

博士生导师

硕士生导师

性别:女

毕业院校:大连理工大学

学位:博士

所在单位:化工学院

学科:化学工艺. 能源化工. 工业催化

办公地点:大连市凌工路2号大连理工大学西部校区化工实验楼C331室

联系方式:0411-84986355

电子邮箱:wencuili@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

Promotion effects of nickel-doped Al2O3-nanosheet-supported Au catalysts for CO oxidation

点击次数:

论文类型:期刊论文

发表时间:2020-02-01

发表刊物:CHINESE JOURNAL OF CATALYSIS

收录刊物:EI、SCIE

卷号:41

期号:2

页面范围:350-356

ISSN号:0253-9837

关键字:Alumina; Gold catalyst; Nickel doping; CO oxidation; Oxygen activation

摘要:Supported gold catalysts show high activity toward CO oxidation, and the nature of the support significantly affects the catalytic activity. Herein, serial Ni doping of thin porous Al2O3 nanosheets was performed via a precipitation-hydrothermal method by varying the amount of Ni during the precipitation step. The prepared nanosheets were subsequently used as supports for the deposition of Au nanoparticles (NPs). The obtained Au/NixAl catalysts were studied in the context of CO oxidation to determine the effect of Ni doping on the supports. Enhanced catalytic performances were obtained for the Au/NixAl catalysts compared with those of the Au supported on bare A1203. The Ni content and pretreatment atmosphere were both shown to influence the catalytic activity. Pretreatment under a reducing atmosphere was beneficial for improving catalytic activity. The highest activity was observed for the catalysts with a Ni/Al molar ratio of 0.05, achieving complete CO conversion at 20 degrees C with a gold loading of 1 wt%. The in-situ FTIR results showed that the introduction of Ni strengthened CO adsorption on the Au NPs. The H-2-TPR and O-2-TPD results indicated that the introduction of Ni produced new oxygen vacancies and allowed the oxygen molecules to be adsorbed and activated more easily. The improved catalytic performance after doping Ni was attributed to the smaller size of the Au NPs and more active oxygen species. (C) 2020, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.