{"title":"Per- and polyfluoroalkyl substances chemical degradation strategies: insights into the underlying reaction mechanisms","authors":"Brian D Etz , Manoj K Shukla","doi":"10.1016/j.coche.2023.100956","DOIUrl":null,"url":null,"abstract":"<div><p>Per- and polyfluoroalkyl substances (PFAS) are highly recalcitrant environmental contaminants that pose a serious threat to living species. As such, many chemical degradation techniques have been proposed and investigated for the efficient destruction of PFAS. A complete and efficient mineralization of high-profile and chemically diverse PFAS contaminants remains an elusive challenge facing society. The underlying reaction mechanisms for PFAS degradation approaches typically involve defluorination, cleavage of the polar head group, or thermal unimolecular reaction. These initial reaction mechanisms and subsequent reaction channels of intermediates will be discussed for various degradation strategies. This contribution aims to highlight recent efforts elucidating PFAS chemical degradation mechanisms to facilitate the advancement of PFAS destruction methods.</p></div>","PeriodicalId":292,"journal":{"name":"Current Opinion in Chemical Engineering","volume":"42 ","pages":"Article 100956"},"PeriodicalIF":8.0000,"publicationDate":"2023-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Opinion in Chemical Engineering","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2211339823000606","RegionNum":2,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Per- and polyfluoroalkyl substances (PFAS) are highly recalcitrant environmental contaminants that pose a serious threat to living species. As such, many chemical degradation techniques have been proposed and investigated for the efficient destruction of PFAS. A complete and efficient mineralization of high-profile and chemically diverse PFAS contaminants remains an elusive challenge facing society. The underlying reaction mechanisms for PFAS degradation approaches typically involve defluorination, cleavage of the polar head group, or thermal unimolecular reaction. These initial reaction mechanisms and subsequent reaction channels of intermediates will be discussed for various degradation strategies. This contribution aims to highlight recent efforts elucidating PFAS chemical degradation mechanisms to facilitate the advancement of PFAS destruction methods.
期刊介绍:
Current Opinion in Chemical Engineering is devoted to bringing forth short and focused review articles written by experts on current advances in different areas of chemical engineering. Only invited review articles will be published.
The goals of each review article in Current Opinion in Chemical Engineering are:
1. To acquaint the reader/researcher with the most important recent papers in the given topic.
2. To provide the reader with the views/opinions of the expert in each topic.
The reviews are short (about 2500 words or 5-10 printed pages with figures) and serve as an invaluable source of information for researchers, teachers, professionals and students. The reviews also aim to stimulate exchange of ideas among experts.
Themed sections:
Each review will focus on particular aspects of one of the following themed sections of chemical engineering:
1. Nanotechnology
2. Energy and environmental engineering
3. Biotechnology and bioprocess engineering
4. Biological engineering (covering tissue engineering, regenerative medicine, drug delivery)
5. Separation engineering (covering membrane technologies, adsorbents, desalination, distillation etc.)
6. Materials engineering (covering biomaterials, inorganic especially ceramic materials, nanostructured materials).
7. Process systems engineering
8. Reaction engineering and catalysis.