Meixia Shan , Chaoqun Niu , Decheng Liu , Dongyang Li , Xueling Wang , Junyong Zhu , Qun Xu , Jorge Gascon , Yatao Zhang
{"title":"Molecular soldered COF membrane with crystalline-amorphous heterointerface for fast organic solvent nanofiltration","authors":"Meixia Shan , Chaoqun Niu , Decheng Liu , Dongyang Li , Xueling Wang , Junyong Zhu , Qun Xu , Jorge Gascon , Yatao Zhang","doi":"10.1016/j.advmem.2024.100110","DOIUrl":null,"url":null,"abstract":"<div><div>Covalent organic frameworks (COFs) featuring high porosity and well-defined pore structures are attractive candidates for organic solvent nanofiltration (OSN). However, preparing defect-free COF membrane and manipulating pore size for precise molecular separation in OSN remains a significant challenge. Herein, we address this challenge by developing composite membranes through molecular soldering a benzimidazole-linked polymer (BILP-101x) onto a continuous ACOF-1 membrane. The shared monomer of ACOF-1 and BILP-101x promotes good compatibility, allowing the amorphous BILP-101x chemically stitch the grain boundary defects of the crystalline ACOF-1 layer and create narrow, staggered pores at the interface, thereby enhancing the OSN performance. Non-equilibrium molecular dynamics simulations were employed to reproduce and explain the permeability order of the solvents and dyes, revealing a hydrogen-bond cluster permeation mode for alcohols. Furthermore, the optimized BILP-101x/ACOF-1 composite membrane exhibits excellent ethanol permeance (13.2 L m<sup>−2</sup> h<sup>−1</sup> bar<sup>−1</sup>) and outstanding rejection towards various dye molecules, together with desirable and stable OSN performance under continuous filtration operation. This work opens a new avenue for improving the separation performance of continuous COF membranes in OSN applications.</div></div>","PeriodicalId":100033,"journal":{"name":"Advanced Membranes","volume":"4 ","pages":"Article 100110"},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Membranes","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772823424000216","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Covalent organic frameworks (COFs) featuring high porosity and well-defined pore structures are attractive candidates for organic solvent nanofiltration (OSN). However, preparing defect-free COF membrane and manipulating pore size for precise molecular separation in OSN remains a significant challenge. Herein, we address this challenge by developing composite membranes through molecular soldering a benzimidazole-linked polymer (BILP-101x) onto a continuous ACOF-1 membrane. The shared monomer of ACOF-1 and BILP-101x promotes good compatibility, allowing the amorphous BILP-101x chemically stitch the grain boundary defects of the crystalline ACOF-1 layer and create narrow, staggered pores at the interface, thereby enhancing the OSN performance. Non-equilibrium molecular dynamics simulations were employed to reproduce and explain the permeability order of the solvents and dyes, revealing a hydrogen-bond cluster permeation mode for alcohols. Furthermore, the optimized BILP-101x/ACOF-1 composite membrane exhibits excellent ethanol permeance (13.2 L m−2 h−1 bar−1) and outstanding rejection towards various dye molecules, together with desirable and stable OSN performance under continuous filtration operation. This work opens a new avenue for improving the separation performance of continuous COF membranes in OSN applications.