Zheng Liu , Yuxuan Sun , Heguo Han , Qifeng Zhang , Shenghai Li , Suobo Zhang
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引用次数: 0
Abstract
Organic solvent nanofiltration (OSN) is an emerging energy-efficient separations technology, which urgently requires easily processable OSN membranes with high selectivity and broad-spectrum organic solvent applicability to facilitate enhanced industrial applications. Herein, we describe the preparation of microporous polyesteramide (PEA) membranes through interfacial polymerization (IP) between amino-diphenol monomers and trimesoyl chloride (TMC) on a poly(ether ether ketone) (PEEK) support. The crosslinked network structures and large twisted monomers enhance the microporosity of PEA membranes, leading to a significant improvement in solvent permeance while maintaining high selectivity. The optimized PEA membrane demonstrates exceptional permeance for acetone (21.0 L m−2 h−1 bar−1) and methanol (14.3 L m−2 h−1·bar−1), with a molecular weight cut-off of 296 g mol−1. Additionally, the PEA/APH-diphenol membrane exhibits ultrafast permeance for the nonpolar solvent toluene (8.3 L m−2 h−1·bar−1), owing to the introduction of a large number of ester groups. Overall, PEA membranes prepared through the molecular-level structure design of IP monomers possess enormous industrial application potential owing to their high performance and broad-spectrum applications.
有机溶剂纳滤(OSN)是一种新兴的高能效分离技术,迫切需要具有高选择性和广谱有机溶剂适用性的易加工OSN膜,以促进工业应用。在此,我们介绍了通过氨基二苯酚单体与三甲基甲酰氯(TMC)在聚醚醚酮(PEEK)载体上的界面聚合(IP)制备微孔聚酯酰胺(PEA)膜的方法。交联网络结构和大扭曲单体提高了 PEA 膜的微孔率,从而在保持高选择性的同时显著改善了溶剂渗透性。优化后的 PEA 膜对丙酮(21.0 L m-2 h-1 bar-1)和甲醇(14.3 L m-2 h-1 bar-1)具有优异的渗透性,截留分子量为 296 g mol-1。此外,由于引入了大量酯基,PEA/APH-二苯酚膜对非极性溶剂甲苯(8.3 L m-2 h-1 bar-1)的渗透率超快。总之,通过对 IP 单体进行分子级结构设计而制备的 PEA 膜因其高性能和广谱应用而具有巨大的工业应用潜力。