Riccardo Mobili, Yue Wu, Charl Xavier Bezuidenhout, Sonia La Cognata, Silvia Bracco, Mariolino Carta and Valeria Amendola
{"title":"Novel CO2-philic porous organic polymers synthesized in water: a leap towards eco-sustainability†","authors":"Riccardo Mobili, Yue Wu, Charl Xavier Bezuidenhout, Sonia La Cognata, Silvia Bracco, Mariolino Carta and Valeria Amendola","doi":"10.1039/D4SU00479E","DOIUrl":null,"url":null,"abstract":"<p >We introduce two novel keto-enamine-linked porous organic polymers (POPs) distinguished by the presence of methyl or ethyl groups in their triamine precursors. These innovative POPs can be synthesized efficiently in water under mild conditions, utilizing starting materials that can be prepared on a gram scale through well-established procedures. Unlike most CO<small><sub>2</sub></small>-philic POPs, which often require organic solvents, high temperatures, catalysts, additives, or hydrothermal equipment, these new polymers are synthesized in pure water at a relatively low temperature (70 °C) without any catalysts or additives and using common glassware. The N-rich composition of these porous organic polymers also contributes to their high adsorption selectivity for CO<small><sub>2</sub></small> over N<small><sub>2</sub></small>, as calculated with the IAST method at 298 K. This combination of environmentally friendly synthesis, high yield, and superior adsorption properties positions these novel POPs as promising candidates for greener carbon capture technologies based on solid sorbents.</p>","PeriodicalId":74745,"journal":{"name":"RSC sustainability","volume":" 11","pages":" 3345-3352"},"PeriodicalIF":0.0000,"publicationDate":"2024-10-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2024/su/d4su00479e?page=search","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"RSC sustainability","FirstCategoryId":"1085","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/su/d4su00479e","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
We introduce two novel keto-enamine-linked porous organic polymers (POPs) distinguished by the presence of methyl or ethyl groups in their triamine precursors. These innovative POPs can be synthesized efficiently in water under mild conditions, utilizing starting materials that can be prepared on a gram scale through well-established procedures. Unlike most CO2-philic POPs, which often require organic solvents, high temperatures, catalysts, additives, or hydrothermal equipment, these new polymers are synthesized in pure water at a relatively low temperature (70 °C) without any catalysts or additives and using common glassware. The N-rich composition of these porous organic polymers also contributes to their high adsorption selectivity for CO2 over N2, as calculated with the IAST method at 298 K. This combination of environmentally friendly synthesis, high yield, and superior adsorption properties positions these novel POPs as promising candidates for greener carbon capture technologies based on solid sorbents.
我们介绍了两种新型酮烯胺键多孔有机聚合物(POPs),它们的区别在于三胺前体中含有甲基或乙基。这些创新型持久性有机污染物可在温和条件下于水中高效合成,使用的起始材料可通过成熟的程序以克级规模制备。与通常需要有机溶剂、高温、催化剂、添加剂或水热设备的大多数亲 CO2 持久性有机污染物不同,这些新型聚合物是在纯水中以相对较低的温度(70 °C)合成的,无需任何催化剂或添加剂,只需使用普通的玻璃器皿。这些多孔有机聚合物富含 N,这也是它们在 298 K 时对 CO2 而非 N2 具有高吸附选择性的原因。这种新型持久性有机污染物集环保合成、高产率和卓越吸附特性于一身,有望成为基于固体吸附剂的绿色碳捕获技术的候选材料。