催化作用
化学
王水
X射线光电子能谱
阳离子聚合
碳纤维
活动站点
无机化学
解吸
活性炭
多相催化
化学工程
有机化学
吸附
金属
材料科学
复合材料
工程类
复合数
作者
Jia Zhao,Bolin Wang,Yuxue Yue,Shuxia Di,Yuanyuan Zhai,Haihua He,Gangfeng Sheng,Huixia Lai,Yihan Zhu,Lingling Guo,Xiao‐Nian Li
标识
DOI:10.1016/j.jcat.2018.06.030
摘要
Gold on activated carbon (Au/AC) materials are promising alternative catalysts for ethyne hydrochlorination. The preparation of active, stable Au/AC catalysts without aqua regia for ethyne hydrochlorination remains a significant challenge. A novel catalyst preparation protocol involving impregnation using a H2O2/HCl mixture is established for highly active Au/AC catalysts comprising primarily of single-site cationic Au species, as identified by systematic X-ray photoelectron spectroscopy (XPS), temperature-programmed reduction (TPR) analyses and transmission electron microscopy (TEM) imaging. In addition, evaluation of the Au-C interface by temperature-programmed desorption (TPD) analyses showed that the oxidation of activated carbon by the H2O2/HCl mixture, which creates surface oxygen-containing functional groups (SOGs), is a crucial step for the formation of active Au/AC catalysts. The structure determination and comprehensive experimental evidence allow density functional theory (DFT) to predict that single-site cationic AuCl species stabilized by SOGs via -O- linkages are efficient active sites for Au-catalyzed ethyne hydrochlorination. In addition, these catalysts can be reused for several times with negligible changes in performance after treatment with the H2O2/HCl mixture. The H2O2/HCl mixture is thus envisioned as a viable, green alternative to toxic aqua regia for the preparation of Au/AC catalysts for ethyne hydrochlorination.
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