环加成
催化作用
环氧化物
锌
材料科学
化学工程
背景(考古学)
离子键合
纳米复合材料
多孔性
聚合物
多相催化
环氧丙烷
离子
化学
有机化学
纳米技术
共聚物
复合材料
冶金
古生物学
工程类
环氧乙烷
生物
作者
Ying Pan,Xiaofei Zhai,Jian Yin,Tianqi Zhang,Liujia Ma,Yi Zhou,Yufeng Zhang,Jianqiang Meng
出处
期刊:Chemsuschem
[Wiley]
日期:2019-03-09
卷期号:12 (10): 2231-2239
被引量:21
标识
DOI:10.1002/cssc.201803066
摘要
Abstract CO 2 cycloaddition to epoxides is an effective and economical utilization method to alleviate the current excessive CO 2 emission situation. The development of catalysts with both high catalytic efficiency and high recyclability is necessary but challenging. In this context, a heterogeneous catalyst was synthesized based on a zinc‐ion‐crosslinked polymer with intrinsic microporosity (PIM‐1). The high microporosity of PIM‐1 promoted a high Zn 2+ loading rate. Additionally, the relatively stable ionic bond formed between Zn 2+ and the PIM‐1 framework through electrostatic interaction ensured high loading stability. In the process of CO 2 cycloaddition with propylene epoxide, an optimized conversion of 90 % with a turnover frequency as high as 9533 h −1 could be achieved within 0.5 h at 100 °C and 2 MPa. After 15 cycles, the catalytic efficiency did not demonstrate a significant decline, and the catalyst was able to recover most of its activity after Zn 2+ reloading. This work thereby provides a strategically designed CO 2 conversion catalyst based on an ionic crosslinked polymer with intrinsic microporosity.
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