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聚醚砜/聚乙烯亚胺共混物的分子相容性与氢键作用机制

Molecular Compatibility and Hydrogen Bonding Mechanism of PES/PEI Blends.

作者信息

Zhu Yuanlu, Wu Weixing, Gao Ming, Yan Jiangyi, Wang Beifu

机构信息

School of Naval Architecture and Shipping, Zhejiang Ocean University, Zhoushan 316000, China.

School of Petrochemical Engineering and Environment, Zhejiang Ocean University, Zhoushan 316000, China.

出版信息

Polymers (Basel). 2022 Jul 27;14(15):3046. doi: 10.3390/polym14153046.

Abstract

The development of high-performance polymer membranes has sparked a lot of attention in recent years. Polymer blending is a potential method of modification. A limitation, however, is the compatibility of blends at the molecular level. In this investigation, polyethersulfone/polyetherimide hollow fiber membranes were prepared by the solution blending method. Compatibility, hydrogen bonding, crystallinity, microstructure, hydrophilicity, mechanical properties, and transmissibility of blended membranes were also characterized. The compatibility and hydrogen bonding action of the two components were confirmed by DSC, FTIR, XPS, and XRD. The structure exhibits a C-H···O interaction motif with the sulfone group acting as a hydrogen bond acceptor from a methyl C-H donor. The π-π stacking between the two polymers arranged molecules more orderly, resulting in enhanced intermolecular interactions. Compared to polyethersulfone hollow fiber membranes, the hydrophilic, mechanical properties, and rejection rate of the blended membranes are more effectively enhanced. Self-assembly of the host polymer with a polymer capable of forming hydrogen bonds to construct controllable blends is a crucial and proven method.

摘要

近年来,高性能聚合物膜的发展引起了广泛关注。聚合物共混是一种潜在的改性方法。然而,一个限制因素是共混物在分子水平上的相容性。在本研究中,采用溶液共混法制备了聚醚砜/聚醚酰亚胺中空纤维膜。还对共混膜的相容性、氢键、结晶度、微观结构、亲水性、力学性能和透过性进行了表征。通过差示扫描量热法(DSC)、傅里叶变换红外光谱法(FTIR)、X射线光电子能谱法(XPS)和X射线衍射法(XRD)证实了两种组分的相容性和氢键作用。该结构呈现出C-H···O相互作用模式,其中砜基作为来自甲基C-H供体的氢键受体。两种聚合物之间的π-π堆积使分子排列更有序,从而增强了分子间相互作用。与聚醚砜中空纤维膜相比,共混膜的亲水性、力学性能和截留率得到了更有效的提高。主体聚合物与能够形成氢键的聚合物进行自组装以构建可控共混物是一种关键且已得到验证的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f86d/9370605/983f6755828f/polymers-14-03046-g001.jpg

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