Promoted carbon dioxide capture via Immobilizing polyethyleneimine and ionic liquid to mesoporous SAPO-34

被引:1
作者
Ye, Nannan [1 ,2 ]
Shen, Yusi [1 ]
Lin, Fei [1 ]
Chen, Yifeng [5 ]
Wang, Zhiheng [1 ]
Zhu, Yudan [1 ,4 ]
Ji, Xiaoyan [3 ]
Lu, Xiaohua [1 ,4 ]
机构
[1] Nanjing Tech Univ, State Key Lab Mat Oriented Chem Engn, Nanjing 211816, Peoples R China
[2] Quzhou Membrane Mat Innovat Inst, Quzhou 324000, Zhejiang, Peoples R China
[3] Lulea Univ Technol, Div Energy Sci Energy Engn, S-97187 Lulea, Sweden
[4] Suzhou Lab, Suzhou 215125, Peoples R China
[5] CAF, Key & Open Lab Forest Chem Engn, Key Lab Biomass Energy & Mat, Natl Engn Lab Biomas,Inst Chem Ind Forest Prod,SFA, Nanjing 210042, Peoples R China
基金
中国国家自然科学基金;
关键词
CO2; capture; Mesoporous SAPO-34; Poly(ethylenimine); Bmim][Ac; CO2; CAPTURE; PEI; PERFORMANCE; ADSORBENTS; REGENERATION; ABSORPTION; ADSORPTION; EFFICIENT; SBA-15;
D O I
10.1016/j.seppur.2025.132356
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The main challenges encountered for supported amine sorbents in carbon dioxide (CO2) capture are the low CO2 diffusion and high desorption heat. In this work, we immobilized a mixture of low-viscosity ionic liquid (IL) 1-butyl-3-methylimidazole acetate with high affinity for CO2 and polyethyleneimine (PEI) onto the prepared mesoporous molecular sieve SAPO-34. The apparent sorption/desorption rates were enhanced distinctly, and the time to reach equilibrium was shortened down to 30 min. For comparison, the corresponding time for SAPO-34-PEI was up to 150 min. A low desorption heat of approximately 1.281 to 1.423 GJ t(-1) CO2 was achieved, which is lower than that of the PEI-loaded materials with a value > 1.5 GJ t(-1) CO2. Meanwhile, the hybrid sorbent (SAPO-34-PEI-IL) enhanced CO2 sorption capacities compared to SAPO-34-PEI and SAPO-34-IL, i.e., 135 % and 137 % increases, respectively, and exhibited excellent sorption-desorption cycle stability, retaining over 95 % of the initial sorption capacity after 24 cycles. This work presents a novel approach for the supported amine sorbent to be utilized for CO2 capture in the future.
引用
收藏
页数:12
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