卢金凯, 张梦, 初秉宪, 金理健, 肖健泽, 李斌, 董丽辉, 范闽光. 环状碳酸酯的固载型离子液体催化合成[J]. 华南师范大学学报(自然科学版), 2021, 53(6): 43-49. doi: 10.6054/j.jscnun.2021091
引用本文: 卢金凯, 张梦, 初秉宪, 金理健, 肖健泽, 李斌, 董丽辉, 范闽光. 环状碳酸酯的固载型离子液体催化合成[J]. 华南师范大学学报(自然科学版), 2021, 53(6): 43-49. doi: 10.6054/j.jscnun.2021091
LU Jinkai, ZHANG Meng, CHU Bingxian, JIN Lijian, XIAO Jianze, LI Bin, DONG Lihui, FAN Minguang. The Synthesis of Cyclic Carbonate Catalyzed by Immobilized Ionic Liquid[J]. Journal of South China Normal University (Natural Science Edition), 2021, 53(6): 43-49. doi: 10.6054/j.jscnun.2021091
Citation: LU Jinkai, ZHANG Meng, CHU Bingxian, JIN Lijian, XIAO Jianze, LI Bin, DONG Lihui, FAN Minguang. The Synthesis of Cyclic Carbonate Catalyzed by Immobilized Ionic Liquid[J]. Journal of South China Normal University (Natural Science Edition), 2021, 53(6): 43-49. doi: 10.6054/j.jscnun.2021091

环状碳酸酯的固载型离子液体催化合成

The Synthesis of Cyclic Carbonate Catalyzed by Immobilized Ionic Liquid

  • 摘要: 通过烷基化反应和简单的一锅法将醇胺离子液体(TEA)嫁接到氯甲基聚苯乙烯(PS-Cl)微球上,将形成的嫁接型离子液体催化剂(PS-TEAI)用于催化CO2和环氧化物生成环状碳酸酯的反应. 采用傅里叶变换红外光谱(FT-IR)和扫描电子显微镜(SEM)表征催化剂的结构和形貌,采用X射线光电子能谱(XPS)、元素分析(EA)和热重分析(TGA)研究了醇胺离子液体的嫁接量和热稳定性. 在环加成反应中,该催化剂无需溶剂和助催化剂,在催化剂用量为0.10 g、温度为120 ℃、CO2压力为2 MPa以及反应时间为4 h的条件下,碳酸丙烯脂(PC)的产率达到93.30%,并且反应后容易分离,可重复使用. 最后提出了羟基形成的氢键可激活环氧化物和I-亲核进攻促进开环的反应机理.

     

    Abstract: The alcohol amine ionic liquid (TEA) was grafted onto chloromethyl polystyrene (PS-Cl) microspheres through alkylation reaction and the simple one-pot method and the resulting ionic liquid-supported catalyst (PS-TEAI) was used to catalyze the formation of cyclic carbonates from carbon dioxide and epoxides. The structure and morphology of the catalyst were characterized with the Fourier transform infrared spectroscopy (FT-IR) and the scanning electron microscope (SEM). The grafting amount and the thermal stability of alcohol amine ionic liquids were studied with the X-ray photoelectron spectroscopy (XPS), the elemental analysis (EA) and the thermogravimetric analysis (TGA). In the cycloaddition reaction, the catalyst did not require solvents and co-catalysts. Under the experimental conditions of catalyst dosage of 0.10 g, 120 ℃ temperature, 2 MPa CO2 pressure and 4 h reaction time, the yield of propylene carbonate (PC) reached 93.30%. It was easy to separate after the reaction and could be reused. The reaction mechanism of hydrogen bond formed with hydroxyl activating epoxide and I- nucleophilic attack to promote ring opening was finally proposed.

     

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