Urea modified USY zeolite supported Cu-based catalyst for acetylene hydrochlorination

被引:1
作者
Dang, Lei [1 ]
Wang, Lu [1 ,3 ]
Yan, Haijun [1 ]
Gong, Bingbing [1 ]
Yang, Chao [1 ]
Wang, Jide [1 ]
Sun, Hui [1 ,2 ]
Li, Xiaofei [3 ]
Wu, Ronglan [1 ]
Liang, Changhai [4 ]
机构
[1] Xinjiang Univ, Sch Chem Engn, Key Lab Oil & Gas Fine Chem, Minist Educ & Xinjiang Uygur Autonomous Reg, Urumqi 830017, Peoples R China
[2] East China Univ Sci & Technol, Sch Chem Engn, State Key Lab Chem Engn, Shanghai 200237, Peoples R China
[3] Xinjiang Uygur Autonomous Reg Prod Qual Supervis &, Urumqi 830011, Peoples R China
[4] Dalian Univ Technol, State Key Lab Fine Chem, Dalian 116086, Peoples R China
来源
MATERIALS TODAY COMMUNICATIONS | 2024年 / 40卷
基金
中国国家自然科学基金;
关键词
USY zeolite; Cu catalysis; Reaction mechanism; Acetylene hydrochlorination; MERCURY-FREE CATALYSTS; IONIC LIQUID; EFFICIENT; STABILITY; PROGRESS;
D O I
10.1016/j.mtcomm.2024.110070
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Zeolites have been used as a new support for noble catalysts in acetylene hydrochlorination, but the possibility of loading non-noble catalysts is often ignored. Herein, a series of Cu-based/USY catalysts were prepared, among which Cu-Urea/USY catalysts performed better. A combination of experimental and theoretical techniques reveals that the coordination of urea and CuCl2 balances the adsorption energy of the reactants on the catalyst, thereby reducing the formation of carbon deposition and improving the catalytic performance. The reaction is carried out by the L-H mechanism. This work provides a strategy for the synthesis of high performance zeolites supported Cu-based catalysts during acetylene hydrochlorination.
引用
收藏
页数:7
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