N-doped porous polymer with protonated ionic liquid sites for efficient conversion of CO2 to cyclic carbonates

被引:15
|
作者
Cai, Heshan [1 ]
Chen, Junji [1 ]
Cai, Kaixing [1 ]
Liu, Fei [1 ]
Zhao, Tianxiang [1 ]
机构
[1] Guizhou Univ, Sch Chem & Chem Engn, Key Lab Green Chem & Clean Energy Technol, Guiyang 550025, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
CO2; N-doped porous polymer; Ionic liquid; Cyclic carbonate; ORGANIC POLYMER; GRAPHENE OXIDE; CATALYST; CYCLOADDITION; EPOXIDES; FIXATION; PRESSURE; MILD; DIOXIDE; CAPTURE;
D O I
10.1016/j.micromeso.2023.112447
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A N-doped porous polymer with protonated ionic liquid sites was fabricated by a solvent-free self-assembly synthesis of resorcinol/formaldehyde resin, followed by modification with hydrobromic acid (HBr) to introduce ionic sites. Compared with the parent polymer PIP-HP, polymer PIP-HP-HBr maintains a high specific surface area after ion site construction, and the elevated activity was also acquired under metal/solvent/cocatalyst-free conditions with up to 99% yield of cyclic carbonates. Furthermore, the PIP-HP-HBr as a heterogeneous catalyst can be readily recovered and demonstrate excellent cycling stability. In addition, a plausible catalytic mechanism had been proposed that the high catalytic activity originates from the synergistic effect of hydrogen bond donor -OH and nucleophilic anion Br-.
引用
收藏
页数:8
相关论文
共 50 条
  • [1] Polymeric Ionic Liquid Grafted on Silica for Efficient Conversion of CO2 into Cyclic Carbonates
    Ying, Ting
    Su, Qian
    Shi, Zijie
    Deng, Lili
    Cheng, Weiguo
    Hua, Wei
    CATALYSIS LETTERS, 2019, 149 (10) : 2647 - 2655
  • [2] Synergistic catalysis of hypercrosslinked ionic polymers with multi-ionic sites for conversion of CO2 to cyclic carbonates
    Liao, Xu
    Wang, Zeyu
    Kong, Lingzheng
    Gao, Xilin
    He, Jiao
    Huang, Dongha
    Lin, Jinqing
    MOLECULAR CATALYSIS, 2023, 535
  • [3] Facile syntheses of ionic polymers for efficient catalytic conversion of CO2 to cyclic carbonates
    Zhang, Yiwen
    El-Sayed, El-Sayed M.
    Su, Kongzhao
    Yuan, Daqiang
    Han, Zhengbo
    JOURNAL OF CO2 UTILIZATION, 2020, 42
  • [4] Pore engineering of ultramicroporous carbon from an N-doped polymer for CO2 adsorption and conversion
    Cai, Heshan
    Fu, Lin
    Pan, Hongyan
    Yan, Zaixin
    Chen, Teng
    Zhao, Tianxiang
    MOLECULAR CATALYSIS, 2023, 550
  • [5] Polyamine-functionalized imidazolyl poly(ionic liquid)s for the efficient conversion of CO2 into cyclic carbonates
    Zou, Yizhen
    Ge, Yuansheng
    Zhang, Qiang
    Liu, Wei
    Li, Xiaoguang
    Cheng, Guoe
    Ke, Hanzhong
    CATALYSIS SCIENCE & TECHNOLOGY, 2022, 12 (01) : 273 - 281
  • [6] Gradient poly(ionic liquid)s with sequence modulation for catalytic CO2 conversion into cyclic carbonates
    Zhao, Qianmeng
    Chen, Jian
    Fu, Mengqian
    Deng, Lili
    Li, Yunong
    Su, Qian
    Cheng, Weiguo
    APPLIED MATERIALS TODAY, 2023, 35
  • [7] Anion-rich porous poly(ionic liquid)s for efficient CO2 conversion into cyclic carbonates through hydrogen bonding synergistic effect
    Liao, Quanlan
    Wang, Xiaoqing
    Zhao, Fangfang
    Zhao, Tiaxniang
    Cao, Jianxin
    MOLECULAR CATALYSIS, 2024, 552
  • [8] Renewable N-doped active carbons as efficient catalysts for direct synthesis of cyclic carbonates from epoxides and CO2
    Samikannu, Ajaikumar
    Konwar, Lakhya Jyoti
    Maki-Arvela, Paivi
    Mikkola, Jyri-Pekka
    APPLIED CATALYSIS B-ENVIRONMENTAL, 2019, 241 : 41 - 51
  • [9] Imidazolium-based polymeric ionic liquids for heterogeneous catalytic conversion of CO2 into cyclic carbonates
    Wang, Yinpeng
    Nie, Junqi
    Lu, Cuifen
    Wang, Feiyi
    Ma, Chao
    Chen, Zuxing
    Yang, Guichun
    MICROPOROUS AND MESOPOROUS MATERIALS, 2020, 292
  • [10] Efficient conversion of CO2 into cyclic carbonates under atmospheric by halogen and metal-free poly(ionic liquid)s
    Jiang, Bowen
    Liu, Jia
    Yang, Guoqiang
    Zhang, Zhibing
    CHINESE JOURNAL OF CHEMICAL ENGINEERING, 2023, 55 : 202 - 211