共聚物
膜
相位反转
材料科学
化学工程
PEG比率
高分子化学
超滤(肾)
两亲性
溶剂
接触角
复合材料
聚合物
色谱法
化学
有机化学
工程类
经济
生物化学
财务
作者
Enrique Folgado,Vincent Ladmiral,Mona Semsarilar
标识
DOI:10.1016/j.eurpolymj.2020.109708
摘要
Poly(vinylidene fluoride) (PVDF) ultrafiltration membranes were prepared by non-solvent-induced phase separation (NIPS) using a blend of a new amphiphilic PVDF-based triblock copolymer (PVDF-b-PEG-b-PVDF) and high molar mass PVDF. During the phase inversion step, the triblock copolymer acts both as a pore forming and surface modifying agent. Thanks to the presence of the short PVDF blocks in the triblock copolymer, the hydrophilic PEG segment is fixed in the PVDF matrix, thus reducing the gradual loss of hydrophilic additive by leaching of the triblock copolymer out of the membrane matrix. The PVDF-b-PEG-b-PVDF triblock copolymer additive improved the surface hydrophilicity and significantly increased the pure water flux and permeability of the PVDF membrane. The membrane composition was optimized in terms of additive concentration and compared to membranes prepared with an equivalent amount of commercial PEG of similar molar mass. Pure water filtration tests and contact angle measurements suggested that addition of small amounts of the triblock copolymer additive (2–5% w/w) has a strong impact on the performance and hydrophilic characteristic of the PVDF membranes. The control tests showed that less than 30% w/w of the additive is lost after 9 months, while most commercial PEG (59% w/w) leached out of the membrane matrix in only two months.
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