纳滤
膜
聚酰胺
聚偏氟乙烯
化学工程
渗透
界面聚合
聚砜
材料科学
结垢
海水淡化
高分子化学
单体
化学
聚合物
复合材料
渗透
工程类
生物化学
作者
Jinyu Li,Xuewu Zhu,Xiaoxiang Cheng,Jin Wang,Weiwei Zhou,Cunxian Lai,Daoji Wu,Feiyong Chen,Fengxun Tan,Heng Liang
标识
DOI:10.1021/acsapm.2c00277
摘要
Conventional polysulfone and polyethersulfone membrane-supported polyamide (PA) nanofiltration (NF) membranes suffer an obvious performance decline due to the drastic pore shrinkage of their membranes during high-temperature (HT) desalination processes. Herein, a thermally stable PA NF membrane (PVDF-IP-2) was successfully constructed over a relatively hydrophobic polyvinylidene fluoride (PVDF) membrane using a continuous interfacial polymerization (CIP) method. The PVDF-IP-2 membrane had a moderate water permeance of 8.3 L m–2 h–1 bar–1 and a 99.7% Na2SO4 rejection at room temperature, which were comparable to those of commercial NF membranes. Introducing calcium ions (Ca2+) into the aqueous solutions further confined the transport rate of the piperazine monomer across the reaction interface through the coordination functions between Ca2+ and piperazine molecules, forming a high-flux (15.9 L m–2 h–1 bar–1 at room temperature) NF membrane (PVDF-IP-Ca) with an excellent Na2SO4 rejection (∼98.6%). Impressively, the PVDF-IP-Ca membrane presented an excellent antifouling behavior and performance stability during both fouling and high-temperature filtration tests. The Ca2+-assisted IP (Ca–CIP) strategy is expected to be a facile and universal approach to preparing TFC desalination membranes for HT environmental applications on relatively hydrophobic supports.
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