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Tuning the molecular design of random copolymers for enhancing the biofouling mitigation of membrane materials

Although a lot has been done on the making of antifouling membranes using PEGylated materials, numerous molecular design improvements can still be made on fine-tuning of both composition and chain length. Here, an antifouling copolymer made of styrene and ethylene glycol methacrylate units (PS-co-PE...

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Bibliographic Details
Published in:Journal of membrane science 2019-10, Vol.588, p.117217, Article 117217
Main Authors: Maggay, Irish Valerie, Yeh, Tso-Hsuan, Venault, Antoine, Hsu, Chen-Hua, Dizon, Gian Vincent, Chang, Yung
Format: Article
Language:English
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Summary:Although a lot has been done on the making of antifouling membranes using PEGylated materials, numerous molecular design improvements can still be made on fine-tuning of both composition and chain length. Here, an antifouling copolymer made of styrene and ethylene glycol methacrylate units (PS-co-PEGMA) was used and the results demonstrate that by altering the molar ratio and chain length PS/PEGMA, it can turn the membrane from low-biofouling to almost entirely fouling resistant. At first, a set of 7 copolymers with a molecular weight in a same range but different compositions was prepared, characterized and was used to modify poly(vinylidene fluoride) (PVDF) membranes by vapor-induced phase separation (VIPS) process. Membranes were fully characterized, and antifouling tests carried out with Escherichia coli, Stenotrophomonas maltophilia and fibrinogen all showed that a 30 mol% polystyrene content in the copolymer (PS30P70) led to the best antifouling properties. Increasing or decreasing the styrene amount resulted in increasing the hydrophobicity of the material or decreasing the stability of the modification, respectively, which outcome in both cases was a higher biofouling. Then, 5 copolymers with a fixed composition but different Mws were prepared, and antifouling tests indicated that the longer the chain, the better the antifouling properties. The chain length is essential to the strength of the hydration layer as supported by both mapping FT-IR and DSC measurements. [Display omitted] •A series of antifouling copolymers with varying composition/chain length is presented.•Antifouling bi-continuous membranes are prepared by vapor-induced phase separation.•The composition affects the balance between stability and antifouling property.•The chain length affects the strength of the hydration layer.•Very low biofouling is obtained with the optimized membrane.
ISSN:0376-7388
1873-3123
DOI:10.1016/j.memsci.2019.117217