TY - JOUR
T1 - Ultrathin PEI-functionalized carboxyl covalent organic framework membranes for efficient CO2/N2 separation
AU - Zeng, Shichen
AU - Liang, Xu
AU - Zhao, Mingang
AU - Ren, Yanxiong
AU - Ma, Hanze
AU - Zhu, Ziting
AU - Wang, Yuhan
AU - Wang, Shaoyu
AU - Zhao, Junyi
AU - Yang, Guangzhaoyao
AU - Wang, Xuerui
AU - Pan, Fusheng
AU - He, Guangwei
AU - Jiang, Zhongyi
N1 - Publisher Copyright:
© 2024 Elsevier B.V.
PY - 2024/4
Y1 - 2024/4
N2 - Covalent organic frameworks (COF) are deemed as disruptive membrane materials owing to their versatile functionalities, high stability and ordered nanochannels. However, the size mismatch between the COF intrinsic pore and gas molecules becomes a grand challenge when using COF membrane for carbon capture. Herein, we propose a new type of polymer-functionalized COF laminar membranes through grafting CO2-phlic polyethyleneimine (PEI) polymer onto carboxylic acid COF (cCOF) laminar membranes. The cCOF nanosheets with high density of carboxyl groups are prepared via modified single phase solution method and then assembled to fabricate membranes. Further, the cCOF membranes are functionalized with PEI using 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide/N-Hydroxysuccinimide (EDC/NHS) coupling chemistry. The introduction of abundant amino groups from PEI afford the affinity of membranes toward CO2. Meanwhile, the graft of the PEI polymers reduces the defects or pinholes on the membrane surface. As a result, the PEI functionalized cCOF membranes exhibit a high CO2 permeance of 1004 GPU and a CO2/N2 selectivity of 33.7, which reach the carbon capture target performance and show great prospect for treating real flue gas. Our approach of functionalizing cCOF membranes with tailored functionalities may inspire the design of molecule-selective COF membranes.
AB - Covalent organic frameworks (COF) are deemed as disruptive membrane materials owing to their versatile functionalities, high stability and ordered nanochannels. However, the size mismatch between the COF intrinsic pore and gas molecules becomes a grand challenge when using COF membrane for carbon capture. Herein, we propose a new type of polymer-functionalized COF laminar membranes through grafting CO2-phlic polyethyleneimine (PEI) polymer onto carboxylic acid COF (cCOF) laminar membranes. The cCOF nanosheets with high density of carboxyl groups are prepared via modified single phase solution method and then assembled to fabricate membranes. Further, the cCOF membranes are functionalized with PEI using 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide/N-Hydroxysuccinimide (EDC/NHS) coupling chemistry. The introduction of abundant amino groups from PEI afford the affinity of membranes toward CO2. Meanwhile, the graft of the PEI polymers reduces the defects or pinholes on the membrane surface. As a result, the PEI functionalized cCOF membranes exhibit a high CO2 permeance of 1004 GPU and a CO2/N2 selectivity of 33.7, which reach the carbon capture target performance and show great prospect for treating real flue gas. Our approach of functionalizing cCOF membranes with tailored functionalities may inspire the design of molecule-selective COF membranes.
KW - Carbon capture
KW - Covalent organic framework
KW - Gas separation membrane
KW - Polyethyleneimine
KW - Polymer functionalization
UR - http://www.scopus.com/inward/record.url?scp=85186387379&partnerID=8YFLogxK
U2 - 10.1016/j.memsci.2024.122590
DO - 10.1016/j.memsci.2024.122590
M3 - 文章
AN - SCOPUS:85186387379
SN - 0376-7388
VL - 698
JO - Journal of Membrane Science
JF - Journal of Membrane Science
M1 - 122590
ER -