埃洛石
离子液体
环加成
催化作用
路易斯酸
化学
无机化学
吸附
解吸
介孔材料
离子键合
碳酸丙烯酯
化学工程
材料科学
有机化学
离子
物理化学
工程类
电化学
电极
作者
Jiangtao Peng,Haowei Sun,Jian Wang,Peiping Zhang,Weikun Ning,Yan Wang,Wei Zhang,Wenqing Li,Cundi Wei,Shiding Miao
标识
DOI:10.1016/j.clay.2021.106329
摘要
A type of clay-supported catalysts were developed for conversion of CO 2 by encapsulating ZnBr 2 -based Lewis acidic ionic liquids (ZnBr 2 /IL) in halloysite (Hal) via a one-step strategy. The Lewis acidic ionic liquid was loaded within enlarged lumens of Hal via acid treatment, and the mesoporous structure was found to benefit for CO 2 storage/conversion. The composite ZnBr 2 /IL@P-Hal was found to have an adsorption capacity (6.43 cm 3 /g) of CO 2 via adsorption/desorption isotherm measurements. The composite ZnBr 2 /IL@P-Hal showed excellent catalytic performance (TOF value was 1747.7 h −1 ) for coupling of CO 2 with epoxides to produce propylene carbonate under the lack of any cocatalyst . Kinetic investigations indicated the reaction followed an order of one, with respect to catalyst ZnBr 2 /IL@P-Hal. The overall pathway of CO 2 cycloaddition was theoretically validated via DFT calculations. These experimental and computational efforts deepen comprehension of the rational design of clay-based catalysts for CO 2 cycloaddition, further elucidated halloysite was a promising support. • Halloysite was encapsulated with Lewis acidic ionic liquids and ZnBr 2 . • The lumen of halloysite was enlarged to load ionic liquids. • Better adsorption of CO 2 and excellent catalytic performance were obtained. • DFT was done to reveal the pathway of CO 2 cycloaddition.
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