Zn,N co-doped 3D carbon frameworks constructed by in-situ polymerization-pyrolysis of fluid precursors and their applications in boosting atmospheric CO2 capture and fixation

被引:6
|
作者
Ma, Chi [1 ]
Zhang, Han [1 ]
Zhang, Guojie [2 ]
Liu, Fusheng [1 ]
Wang, Dongchao [3 ]
Ma, Jingjing [4 ]
Liu, Mengshuai [1 ]
机构
[1] Qingdao Univ Sci & Technol, Coll Chem Engn, State Key Lab Base Ecochem Engn, Qingdao 266042, Peoples R China
[2] Taiyuan Univ Technol, State Key Lab Clean & Efficient Coal Utilizat, Taiyuan 030024, Peoples R China
[3] Shandong Chambroad Petrochem Co Ltd, Binzhou 256500, Peoples R China
[4] Ningxia Univ, State Key Lab High efficiency Utilizat Coal & Gree, Yinchuan 750021, Peoples R China
基金
中国国家自然科学基金;
关键词
3D carbon framework; CO 2 capture and conversion; Multifunction catalyst; Cyclic carbonate; Heterogeneous catalysis; CATALYST; DIOXIDE; ADSORPTION; REDUCTION; LIQUID;
D O I
10.1016/j.seppur.2023.125196
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Through the rational design of 1-butyl-3-methylimidazolium bis((trifluoromethyl)sulfonyl)imide ([Bmim] [NTf2])-based multi-component fluid precursors, we present a novel and sustainable strategy for preparing Zn,N co-doped 3D carbon frameworks (Zn@CTDPOP-IL) via in-situ polymerization-pyrolysis of fluid precursors, and explore their applications in atmospheric CO2 capture and clean conversion into cyclic carbonates. The structure and performance of Zn@CTDPOP-IL frameworks were optimized by preparing them under different pyrolysis temperatures and fluid precursor compositions. It was found that the in-situ polymerization of aldehyde and amine components in fluid precursors was crucial for achieving a high specific surface area of carbon frameworks; [Bmim][NTf2] was used as both the solvent and catalyst for in-situ polymerization, as well as the soft template agent during subsequent pyrolysis process. The carbon frameworks also possess multiple Lewis acid/ base active sites, exhibiting excellent CO2 adsorption (3340 mu mol/g) and conversion performance under mild (40 degrees C, 0.1 MPa) and solvent-free conditions. The cyclic carbonate yield reaches up to 94 % with a selectivity of 99 %, which is attributed to the superior activation abilities of Lewis acid/base sites towards epoxide and CO2 respectively. The reusability and universality of the catalyst were further investigated, revealing its exceptional structural stability and satisfactory versatility. Finally, we elucidated a proposed cycloaddition mechanism catalyzed by multiple active sites in Zn@CTDPOP-IL. Compared to other reported porous carbon materials, the Zn@CTDPOP-IL frameworks developed herein are simple and environmentally friendly in preparation while exhibiting excellent dual functionality for CO2 adsorption and catalytic conversion, making them highly promising for cleaner treatment of low-pressure waste CO2 resource.
引用
收藏
页数:11
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