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Synergistic effect of a binary ionic liquid/base catalytic system for efficient conversion of epoxide and carbon dioxide into cyclic carbonates

机译:二元离子液/碱催化系统的协同作用,以便将环氧化物和二氧化碳转化为环状碳酸酯

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Carbon dioxide (CO2) mitigation via utilization can be a potential solution to global warming issues such as increasing CO2 concentration. In this study, we present the synthesis and characterisation of 3-(2-hydroxyethyl)-1-vinyl-1H-imidazol-3-ium chloride [EvimOH][Cl] and 3-(2-hydroxyethyl)-1-vinyl-1H-imidazol-3-ium sulphate [EvimOH][HSO4] ionic liquids for cycloaddition reactions of CO2 and epoxides into cyclic carbonates. The synthesized ionic liquids were characterized by FT-IR, H-1- and C-13-NMR spectroscopic methods. Also, we have analysed the physical properties of ionic liquids by using TGA and DTA. Further, the CO2 consumption was done by developing a binary catalytic system with bases such as DBU, TEA, DIPEA, piperidine, pyrrolidine, aniline. The developed binary ([EvimOH][Cl]/base) catalytic system exhibited the excellent catalytic activity of 99.8% conversion and >= 99% selectivity under mild reaction conditions without the aid of solvent and metal co-catalysts. Furthermore, the results show that the improved activity from the binary system is due to synergistic effect among -OH functional group from the cation, reactive acidic C(2)-H in the imidazolium ring and amine containing bases which promote the CO2 absorption. Also, a plausible mechanism of cyclic carbonate formation and kinetic study in the presence of binary catalytic system was demonstrated.
机译:通过利用的二氧化碳(CO2)缓解可以是全球变暖问题的潜在解决方案,例如增加CO 2浓度。在这项研究中,我们介绍了3-(2-羟乙基)-1-乙烯基-1H-咪唑-3-氯化物[EVIMOH] [Cl]和3-(2-羟基乙基)-1-乙烯基 - 的合成和表征1H-咪唑-3-Ium硫酸盐[EVIMOH] [HSO4]离子液体用于CO 2和环氧化物的环加成反应至环碳酸酯。通过FT-IR,H-1-和C-13-NMR光谱方法表征合成的离子液体。此外,我们通过使用TGA和DTA分析了离子液体的物理性质。此外,通过开发具有DBU,茶叶,DIPEA,哌啶,吡咯烷,苯胺的基础的二元催化系统来完成二元催化系统。发育的二元([EVIMOH] [Cl] /碱)催化系统表现出优异的催化活性为99.8%转化率和> = 99%的选择性,在不溶剂和金属助催化剂的借助于温和的反应条件下选择性。此外,结果表明,来自二元体系的改善活性是由于来自阳离子,反应性酸性C(2)-H在咪唑鎓环中的反应性酸性C(2)-H和含有促进CO 2吸收的碱基的协同作用。而且,证明了在二元催化系统存在下循环碳酸盐形成和动力学研究的可粘性机制。

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