催化作用
吡啶
离子液体
化学
溴化物
选择性
环氧丙烷
碳酸丙烯酯
亲核细胞
吸附
化学工程
材料科学
聚合物
溶剂
离子键合
产量(工程)
高分子化学
无机化学
有机化学
离子
物理化学
共聚物
环氧乙烷
冶金
工程类
电化学
电极
作者
Chao Liu,Lei Shi,Jiaxu Zhang,Jianmin Sun
标识
DOI:10.1016/j.cej.2021.131633
摘要
A kind of pyridine-based ionic hyper-cross-linked polymers (Py-HCP-X, X = Cl, Br) with high surface area, plentiful hierarchical pores and abundant catalytic active units were prepared via a one-pot method. Adsorption measurements showed that the as-prepared Py-HCP-X exhibited high CO2 capture capacity (up to 1.72 mmol g−1, 273 K and 1 bar). Importantly, Py-HCP-Br displayed excellent catalytic activity for the cycloaddition of CO2 to epoxides under metal/cocatalyst/solvent-free conditions. And the propylene carbonate was produced in 97% yield with an excellent selectivity of 99% at 120 °C and 2.0 MPa CO2 for 8 h. The high performance of the present catalyst is ascribable to synergistic contributions of plentiful hierarchical pores and abundant nucleophilic bromide ions and pyridine-based active units in the Py-HCP-Br catalyst. Additionally, the catalyst is able to be simply separated by centrifugation and reused for four runs without significant loss in the performance, furthermore, the catalyst exhibits great structural stability and substrate universality.
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