Rhea Verbeke , Douglas M. Davenport , Caroline Bogaerts , Samuel Eyley , Wim Thielemans , Ivo F.J. Vankelecom
{"title":"Epoxide-based TFC membranes with tunable performance in the tight nanofiltration range","authors":"Rhea Verbeke , Douglas M. Davenport , Caroline Bogaerts , Samuel Eyley , Wim Thielemans , Ivo F.J. Vankelecom","doi":"10.1016/j.memlet.2023.100054","DOIUrl":null,"url":null,"abstract":"<div><p>Membrane technology offers promise as a breakthrough separation technology in many applications, but is frequently limited by the chemical stability of currently available membrane materials. Recently developed membranes utilizing epoxide-based chemistry have shown great potential as intrinsically stable thin-film composite membranes in water-based applications. However, as these membranes are in their infancy, many synthesis parameters are still to be explored. In this study, the versatility of epoxide chemistry is exploited to demonstrate its potential to serve as a new platform for membrane synthesis, even beyond the field of aqueous applications. It is proven here how the membrane performance can be tailored in a controllable way between 20 – 85% NaCl rejection with a water permeance between 0.5 – 3 L m<sup>−2</sup> h<sup>−1</sup> bar<sup>−1</sup> by simply selecting epoxide monomers and initiators of different size and functionality. A systematic increase in water permeance and salt passage was observed for epoxide monomers that exhibit a lower functionality and a lower number of aromatic groups, while a threshold nucleophilicity and aliphatic chain length of the initiator are required to obtain a salt-selective layer. This work demonstrates the possibility to easily and predictably tune membrane performance in the tight nanofiltration range, while simultaneously achieving a better understanding of the synthesis-structure-performance relationship of this new class of promising membranes.</p></div>","PeriodicalId":100805,"journal":{"name":"Journal of Membrane Science Letters","volume":"3 2","pages":"Article 100054"},"PeriodicalIF":4.9000,"publicationDate":"2023-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Membrane Science Letters","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772421223000181","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Membrane technology offers promise as a breakthrough separation technology in many applications, but is frequently limited by the chemical stability of currently available membrane materials. Recently developed membranes utilizing epoxide-based chemistry have shown great potential as intrinsically stable thin-film composite membranes in water-based applications. However, as these membranes are in their infancy, many synthesis parameters are still to be explored. In this study, the versatility of epoxide chemistry is exploited to demonstrate its potential to serve as a new platform for membrane synthesis, even beyond the field of aqueous applications. It is proven here how the membrane performance can be tailored in a controllable way between 20 – 85% NaCl rejection with a water permeance between 0.5 – 3 L m−2 h−1 bar−1 by simply selecting epoxide monomers and initiators of different size and functionality. A systematic increase in water permeance and salt passage was observed for epoxide monomers that exhibit a lower functionality and a lower number of aromatic groups, while a threshold nucleophilicity and aliphatic chain length of the initiator are required to obtain a salt-selective layer. This work demonstrates the possibility to easily and predictably tune membrane performance in the tight nanofiltration range, while simultaneously achieving a better understanding of the synthesis-structure-performance relationship of this new class of promising membranes.
膜技术有望成为许多应用中的突破性分离技术,但经常受到目前可用膜材料化学稳定性的限制。最近开发的利用环氧基化学的膜在水性应用中显示出作为本质稳定的薄膜复合膜的巨大潜力。然而,由于这些膜还处于起步阶段,许多合成参数仍有待探索。在这项研究中,环氧化物化学的多功能性被用来证明其作为膜合成新平台的潜力,甚至超越了水应用领域。这里证明了如何通过简单地选择不同尺寸和功能的环氧化物单体和引发剂,在20–85%的NaCl截留率和0.5–3 L m−2 h−1 bar−1的透水率之间,以可控的方式调整膜性能。对于表现出较低官能度和较低芳族基团数的环氧化物单体,观察到透水性和盐通道的系统性增加,同时需要引发剂的阈值亲核性和脂肪族链长度来获得盐选择性层。这项工作证明了在严格的纳滤范围内容易且可预测地调节膜性能的可能性,同时更好地理解这类有前途的新型膜的合成结构-性能关系。