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Rationalizing the role of the anion in CO2 capture and conversion using imidazolium-based ionic liquid modified mesoporous silica

机译:使用咪唑基离子液体改性的介孔二氧化硅合理化阴离子在二氧化碳捕获和转化中的作用

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摘要

Covalently supported ionic liquids in mesoporous materials were prepared by grafting 1-methyl-3-(3-trimethoxysylilpropyl)imidazolium chloride in MCM-41. Subsequently, the [Cl-] anion was changed to [BF4-], [PF6-] or [Tf2N-]. These materials that present an advantageous combination of the properties of mesoporous solid materials and ionic liquids were evaluated for CO2 sorption as well as catalysts for CO2 conversion into cyclic carbonate using propylene oxide. The material with the [Cl-] anion had the best performance for both CO2 sorption and conversion. A CO2 sorption of 11 w/w% on the adsorbent was achieved and the cycloaddition reaction exhibited a conversion of 67% with 82% selectivity with the catalyst remaining active after 5 cycles, proving that the same sorbent/catalyst setup can be used for both CO2 capture and conversion. Based on the experimental data and electronic-structure numerical simulations, we have hypothesized two major reasons why chloride out performs other anions when adsorbed on MCM-41 unlike unsupported ionic liquids.
机译:通过将1-甲基-3-(3-三甲氧基甲硅烷基丙基)咪唑鎓氯化物接枝到MCM-41中,制得了介孔材料中共价负载的离子液体。随后,将[Cl-]阴离子变为[BF4-],[PF6-]或[Tf2N-]。对这些具有介孔固体材料和离子液体特性的有利组合的材料进行了CO2吸附以及使用环氧丙烷将CO2转化为环状碳酸酯的催化剂进行了评估。带有[Cl-]阴离子的材料在CO2吸附和转化方面均具有最佳性能。在吸附剂上实现了11 w / w%的CO2吸附,并且环加成反应显示出67%的转化率和82%的选择性,并且催化剂在5个循环后仍保持活性,证明这两种吸附剂/催化剂都可以使用相同的吸附剂/催化剂二氧化碳捕获和转化。基于实验数据和电子结构数值模拟,我们推测了两个主要原因,说明氯离子在吸附在MCM-41上时会表现出其他阴离子,这与不支持的离子液体不同。

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