TY - JOUR
T1 - Electrostatic enhanced surface segregation approach to self-cleaning and antifouling membranes for efficient molecular separation
AU - Long, Mengying
AU - Yang, Chao
AU - You, Xinda
AU - Zhang, Runnan
AU - Yuan, Jinqiu
AU - Guan, Jingyuan
AU - Zhang, Shiyu
AU - Wu, Hong
AU - Khan, Niaz Ali
AU - Kasher, Roni
AU - Jiang, Zhongyi
N1 - Funding Information:
The authors gratefully acknowledge financial support from National Natural Science Foundation of China ( 91934302 , 21961142013 , 22008172 ), Key R&D Program of Zhejiang Province ( 2021C03173 ), Project funded by China Postdoctoral Science Foundation ( 2020TQ0226 ) and Program of Introducing Talents of Discipline to Universities ( BP0618007 ).
Publisher Copyright:
© 2021 Elsevier B.V.
PY - 2021/11/15
Y1 - 2021/11/15
N2 - Membranes with excellent antifouling properties and persistent high permeance are eternal pursuits in membrane technology. Herein, we proposed an electrostatic enhanced surface segregation approach toward the antifouling and self-cleaning membranes for molecular separation. A copolymer containing quaternary ammonium (QA) segments was designed as the surface segregation agent in the casting solution, while polysulphonic acid (PSA) was designed as the crosslinking agent in the coagulation bath. Driven by the electrostatic interactions between the positively charged QA and negatively charged sulphonic groups, the copolymer and PSA were in-situ assembled during the non-solvent induced phase separation (NIPS) processes, generating a selective separation layer on the polymeric matrix. The segregation of copolymer was enhanced, leading to a high surface coverage of ionic QA and sulphonic groups and a significantly improved surface hydrophilicity. Accordingly, the membrane exhibited a high water permeance up to 124 Lm−2h−1bar−1 with dye rejection over 95%. Moreover, the membrane exhibited excellent antifouling performance with the ultralow total permeance decline of 1.2% and the ultrahigh permeance recovery ratio of 99.8% against emulsified oil, as well as the self-cleaning property against crude oil. Hopefully, this study can afford a novel and generic approach to antifouling and self-cleaning membranes for diverse separations.
AB - Membranes with excellent antifouling properties and persistent high permeance are eternal pursuits in membrane technology. Herein, we proposed an electrostatic enhanced surface segregation approach toward the antifouling and self-cleaning membranes for molecular separation. A copolymer containing quaternary ammonium (QA) segments was designed as the surface segregation agent in the casting solution, while polysulphonic acid (PSA) was designed as the crosslinking agent in the coagulation bath. Driven by the electrostatic interactions between the positively charged QA and negatively charged sulphonic groups, the copolymer and PSA were in-situ assembled during the non-solvent induced phase separation (NIPS) processes, generating a selective separation layer on the polymeric matrix. The segregation of copolymer was enhanced, leading to a high surface coverage of ionic QA and sulphonic groups and a significantly improved surface hydrophilicity. Accordingly, the membrane exhibited a high water permeance up to 124 Lm−2h−1bar−1 with dye rejection over 95%. Moreover, the membrane exhibited excellent antifouling performance with the ultralow total permeance decline of 1.2% and the ultrahigh permeance recovery ratio of 99.8% against emulsified oil, as well as the self-cleaning property against crude oil. Hopefully, this study can afford a novel and generic approach to antifouling and self-cleaning membranes for diverse separations.
KW - Antifouling membrane
KW - Dye rejection
KW - Electrostatic interaction
KW - Self-cleaning
KW - Surface segregation
UR - http://www.scopus.com/inward/record.url?scp=85111717238&partnerID=8YFLogxK
U2 - 10.1016/j.memsci.2021.119689
DO - 10.1016/j.memsci.2021.119689
M3 - Article
AN - SCOPUS:85111717238
SN - 0376-7388
VL - 638
JO - Journal of Membrane Science
JF - Journal of Membrane Science
M1 - 119689
ER -