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Photodegradation of fluorotelomer carboxylic 5:3 acid and perfluorooctanoic acid using zinc oxide
Environmental Pollution ( IF 7.6 ) Pub Date : 2018-09-06 , DOI: 10.1016/j.envpol.2018.09.023
Bilal Abada , Theodore E.G. Alivio , Yiru Shao , Thomas E. O'Loughlin , Cory Klemashevich , Sarbajit Banerjee , Arul Jayaraman , Kung-Hui Chu

Occurrence of per- and poly-fluoroalkyl substances (PFASs) in the environment and biota has raised a great concern to public health because these compounds are persistent, bioaccumulative, and toxic. Biodegradation of polyfluoroalkyl substances, particularly long-chain fluorotelomer-based products, can lead to production of various short-chain PFASs, with 5:3 fluorotelomer carboxylic acid (referred as 5:3 FTCA hereafter) as a dominant polyfluoroalkyl metabolite. Perfluoroalkyl acids, particularly perfluorooctanoic acid (PFOA), are toxic and current removal methods are not cost-effective. This study reports the photodegradation of 5:3 FTCA and PFOA using ZnO as a photocatalyst under neutral pH and room temperature conditions. Under long UV wavelength (365 nm), both tetrapod and commercial ZnO can photodegrade 5:3 FTCA. Five removal products-perfluorohexanoic acid, perfluoropentanoic acid, perfluorobutyric acid, 5:2 fluorotelomer carboxylic acid (5:2 FTCA), and inorganic fluoride - were identified, with PFBA and F as dominant end products. SEM and XPS high resolution scans on the surface of the utilized ZnO showed less units of CF2 than that in 5:3 FTCA, supporting occurrence of photodegradation of 5:3 FTCA by ZnO. Defluorination of PFOA was not observed with ZnO only, but at pH 5 and in the co-presence of Fe-citrate. PFOA defluorination increased from 0.93% after 3 days of UV light exposure to 3.9% after additional 135 h under direct sunlight exposure. To the authors’ best knowledge, this is the first report studying ZnO-catalyzed photodegradation of 5:3 FTCA, and examining the Fe co-addition for PFOA defluorination.



中文翻译:

使用氧化锌光降解含氟调聚物5:3酸和全氟辛酸

环境和生物区系中的全氟烷基物质和多氟烷基物质(PFAS)的存在已引起公众极大关注,因为这些化合物具有持久性,生物蓄积性和毒性。多氟烷基物质,特别是长链基于氟调聚物的产品的生物降解,可导致各种短链PFAS的生产,其中5:3氟调聚物羧酸(以下简称5:3 FTCA)为主要的多氟烷基代谢产物。全氟烷基酸,特别是全氟辛酸(PFOA),是有毒的,目前的去除方法并不具有成本效益。这项研究报告了在中性pH和室温条件下使用ZnO作为光催化剂对5:3 FTCA和PFOA的光降解。在长紫外波长(365 nm)下,四脚架和商用ZnO均可光降解5:3 FTCA。作为主要最终产品。在所使用的ZnO表面进行SEM和XPS高分辨率扫描显示,与5:3 FTCA中的CF 2单元相比,CF 2的单元数更少,这支持了ZnO对5:3 FTCA的光降解。不仅在ZnO上观察到PFOA的脱氟,在pH为5且柠檬酸铁共存的情况下也未观察到PFOA的脱氟。PFOA的脱氟从紫外线暴露3天后的0.93%增加到直接在阳光直射下另外135小时后的3.9%。据作者所知,这是第一份研究ZnO催化5:3 FTCA光降解并研究Fe共添加的PFOA脱氟的报告。

更新日期:2018-09-06
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