郭新闻

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教授

博士生导师

硕士生导师

主要任职:盘锦校区管委会副主任兼教学与科研工作部部长

性别:男

毕业院校:大连理工大学

学位:博士

所在单位:化工学院

学科:工业催化. 物理化学

办公地点:化工实验楼B427

联系方式:18641143913

电子邮箱:guoxw@dlut.edu.cn

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Organic acid-assisted preparation of highly dispersed Co/ZrO2 catalysts with superior activity for CO2 methanation

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论文类型:期刊论文

发表时间:2019-10-05

发表刊物:APPLIED CATALYSIS B-ENVIRONMENTAL

收录刊物:SCIE、EI

卷号:254

页面范围:531-540

ISSN号:0926-3373

关键字:CO2 methanation; Cobalt catalyst; ZrO2; Organic acid; High dispersion

摘要:Various organic acids were investigated for preparing the highly dispersed cobalt catalysts on zirconia support, Co/ZrO2, by an acid-assisted incipient wetness impregnation. The organic acid-assisted preparation results in highly dispersed Co/ZrO2 catalysts which demonstrate superior catalytic activity with only 2 wt.% Co loading for CO2 methanation. Among the acids, the carboxylic acids with bigger molecular weight, more carboxyl groups and hydroxyl groups are more effective. Furthermore, the amino acids can also change the charge property of ZrO2 surface through controlling the solution pH and increase the metal dispersion through strong electrostatic adsorption. It is worth mentioning that, among the numerous organic acids, citric acid-assisted preparation gives Co/ZrO2 catalyst with superior catalytic activity and increased the CO2 conversion from 38% to 85% with highest turnover frequency. The linear relationship between metal dispersion and TOF with the molar ratio of acid to cobalt n(CA/Co) ranging from 0 to 2 demonstrates the importance of well dispersed metal particles in the enhanced activity. However, when the n(CA/Co) value exceeds 2 and the metal particle size further decreases, but no further enhancement is observed and the CO2 conversion even slightly decreased at the n(CA/Co) value of 5. The organic acids-assisted strategy can lead to increased metal dispersion and higher TOF for Co/ZrO(2 )catalysts; the appropriate metal dispersion corresponds to the suitable Co/ZrO2 interaction with oxygen vacancy which leads to more catalytically active sites for CO2 adsorption and catalytic hydrogenation. The organic acid-assisted strategy provides a new design approach for highly dispersed and active catalysts.