CO2-selective transport in PEGDA facilitated transport membranes post-functionalized using click chemistry

IF 8.4 1区 工程技术 Q1 ENGINEERING, CHEMICAL Journal of Membrane Science Pub Date : 2025-02-11 DOI:10.1016/j.memsci.2025.123825
Ryan A. Johnson, Zoe Reddecliff, Karim El Hajj Sleiman, Joshua D. Moon
{"title":"CO2-selective transport in PEGDA facilitated transport membranes post-functionalized using click chemistry","authors":"Ryan A. Johnson,&nbsp;Zoe Reddecliff,&nbsp;Karim El Hajj Sleiman,&nbsp;Joshua D. Moon","doi":"10.1016/j.memsci.2025.123825","DOIUrl":null,"url":null,"abstract":"<div><div>A new synthetic strategy to post-functionalize PEGDA membranes using active ester click chemistry was used to study the effects of Lewis base ligand grafting density and basicity on facilitated CO<sub>2</sub> transport and separation. Increasing imidazole ligand content from 0 mol% to 60 mol% causes both CO<sub>2</sub> and N<sub>2</sub> permeabilities to drop by 90+% due to a decrease in gas diffusivities. These diffusivities decrease due to increased chain stiffness from the substitution of flexible PEG groups with stiffer acrylamides. Increasing Lewis basicity of grafted ligands appears to hinder CO<sub>2</sub> diffusion due to stronger interactions between the base and CO<sub>2</sub> resulting in a 60 % decrease in permeability. This decrease in permeability is accompanied by apparent CO<sub>2</sub> chemisorption in piperazine (secondary amine) containing samples and a simultaneous decrease in CO<sub>2</sub> diffusion likely due to immobilization of some CO<sub>2</sub> as carbamate. These findings allow for better understanding of how nitrogenous Lewis base ligands impact CO<sub>2</sub> separations in low T<sub>g</sub> copolymer membranes.</div></div>","PeriodicalId":368,"journal":{"name":"Journal of Membrane Science","volume":"722 ","pages":"Article 123825"},"PeriodicalIF":8.4000,"publicationDate":"2025-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Membrane Science","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0376738825001383","RegionNum":1,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0

Abstract

A new synthetic strategy to post-functionalize PEGDA membranes using active ester click chemistry was used to study the effects of Lewis base ligand grafting density and basicity on facilitated CO2 transport and separation. Increasing imidazole ligand content from 0 mol% to 60 mol% causes both CO2 and N2 permeabilities to drop by 90+% due to a decrease in gas diffusivities. These diffusivities decrease due to increased chain stiffness from the substitution of flexible PEG groups with stiffer acrylamides. Increasing Lewis basicity of grafted ligands appears to hinder CO2 diffusion due to stronger interactions between the base and CO2 resulting in a 60 % decrease in permeability. This decrease in permeability is accompanied by apparent CO2 chemisorption in piperazine (secondary amine) containing samples and a simultaneous decrease in CO2 diffusion likely due to immobilization of some CO2 as carbamate. These findings allow for better understanding of how nitrogenous Lewis base ligands impact CO2 separations in low Tg copolymer membranes.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
研究人员采用一种新的合成策略,利用活性酯点击化学法对 PEGDA 膜进行后功能化,研究了路易斯碱配体接枝密度和碱性对促进二氧化碳传输和分离的影响。咪唑配体含量从 0 摩尔% 增加到 60 摩尔%,会导致二氧化碳和 N2 渗透率下降 90% 以上,原因是气体扩散率降低。这些扩散率的降低是由于用硬度较高的丙烯酰胺取代了柔性 PEG 基团,从而增加了链的硬度。接枝配体的路易斯碱度增加似乎会阻碍二氧化碳的扩散,这是因为碱与二氧化碳之间的相互作用增强,导致渗透性降低 60%。在渗透性降低的同时,在含有哌嗪(仲胺)的样品中出现了明显的二氧化碳化学吸附现象,同时二氧化碳的扩散也有所降低,这可能是由于部分二氧化碳被固定为氨基甲酸酯所致。这些发现有助于更好地了解含氮路易斯碱配体如何影响低 Tg 共聚物膜中的二氧化碳分离。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of Membrane Science
Journal of Membrane Science 工程技术-高分子科学
CiteScore
17.10
自引率
17.90%
发文量
1031
审稿时长
2.5 months
期刊介绍: The Journal of Membrane Science is a publication that focuses on membrane systems and is aimed at academic and industrial chemists, chemical engineers, materials scientists, and membranologists. It publishes original research and reviews on various aspects of membrane transport, membrane formation/structure, fouling, module/process design, and processes/applications. The journal primarily focuses on the structure, function, and performance of non-biological membranes but also includes papers that relate to biological membranes. The Journal of Membrane Science publishes Full Text Papers, State-of-the-Art Reviews, Letters to the Editor, and Perspectives.
期刊最新文献
Highly permeable MOF NH2-MIL-101(Cr) fragment membranes for CO2/N2 separation Editorial Board Amidoxime-functionalized PIM-1 incorporating defect-engineered ZIF-8 for enhanced propylene/propane separation and plasticization resistance Constructing dual hydroxide ion conduction channels with sulfonated hollow carbon spheres for alkaline zinc-based flow battery membrane Multilevel geometric optimization in nanochannel membranes for osmotic energy conversion
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1