{"title":"Rapid Removal of Perfluoroalkanesulfonates from Water by β-Cyclodextrin Covalent Organic Frameworks","authors":"Wei Wang, Haipei Shao, Shuangxi Zhou, Donghai Zhu, Xiangzhe Jiang, Gang Yu, Shubo Deng*","doi":"10.1021/acsami.1c14043","DOIUrl":null,"url":null,"abstract":"<p >Adsorption is an effective method for the removal of perfluoroalkanesulfonates (PFSAs) from water, and the limitation of the adsorption rate of existing adsorbents motivates efforts to develop novel adsorbents. Here, we developed four β-cyclodextrin covalent organic frameworks (β-CD-COFs) with a rapid removal rate and high adsorption capacity for four PFSAs in water including perfluorooctanesulfonate (PFOS), perfluorobutanesulfonate (PFBS), perfluorohexanesulfonate (PFHxS), and chlorinated polyfluorinated ether sulfonate (F53B). All β-CD-COFs exhibited extremely fast adsorption (adsorption equilibrium <2 min) for PFSAs with high adsorption capacities (0.33–1.51 mmol/g), which were significantly better than those of traditional resins and activated carbons, probably due to the ordered pores of β-CD-COFs and the electron-deficient cavity β-CD. Density functional theory (DFT) calculations also showed that PFSAs could be captured in the β-CD cavity through strong interactions with a high binding energy. The novel β-CD-COFs were highly selective to PFSAs in simulated wastewater impacted by aqueous film-forming foams, and they could also rapidly remove them from an actual chrome plating wastewater within 2 min. Additionally, the β-CD-COFs could be regenerated by methanol with relatively good reusability in four cycles, further highlighting their application potential as PFAS adsorbents in water or wastewater.</p>","PeriodicalId":5,"journal":{"name":"ACS Applied Materials & Interfaces","volume":null,"pages":null},"PeriodicalIF":8.3000,"publicationDate":"2021-10-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"14","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Materials & Interfaces","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsami.1c14043","RegionNum":2,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MATERIALS SCIENCE, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 14
Abstract
Adsorption is an effective method for the removal of perfluoroalkanesulfonates (PFSAs) from water, and the limitation of the adsorption rate of existing adsorbents motivates efforts to develop novel adsorbents. Here, we developed four β-cyclodextrin covalent organic frameworks (β-CD-COFs) with a rapid removal rate and high adsorption capacity for four PFSAs in water including perfluorooctanesulfonate (PFOS), perfluorobutanesulfonate (PFBS), perfluorohexanesulfonate (PFHxS), and chlorinated polyfluorinated ether sulfonate (F53B). All β-CD-COFs exhibited extremely fast adsorption (adsorption equilibrium <2 min) for PFSAs with high adsorption capacities (0.33–1.51 mmol/g), which were significantly better than those of traditional resins and activated carbons, probably due to the ordered pores of β-CD-COFs and the electron-deficient cavity β-CD. Density functional theory (DFT) calculations also showed that PFSAs could be captured in the β-CD cavity through strong interactions with a high binding energy. The novel β-CD-COFs were highly selective to PFSAs in simulated wastewater impacted by aqueous film-forming foams, and they could also rapidly remove them from an actual chrome plating wastewater within 2 min. Additionally, the β-CD-COFs could be regenerated by methanol with relatively good reusability in four cycles, further highlighting their application potential as PFAS adsorbents in water or wastewater.
期刊介绍:
ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.