Wen Junying, Li Huarui, Ottosen Lars Ditlev Mørck, Lundqvist Johan, Vergeynst Leendert
Centre for Water Technology (WATEC) & Department of Biological and Chemical Engineering, Aarhus University, Universitetsbyen 36, 8000, Aarhus C, Denmark.
Centre for Water Technology (WATEC) & Department of Biological and Chemical Engineering, Aarhus University, Universitetsbyen 36, 8000, Aarhus C, Denmark; School of Civil Engineering, Yantai University, 30, Qingquan RD, Laishan District, Yantai, 264005, PR China.
Chemosphere. 2023 Dec;344:140344. doi: 10.1016/j.chemosphere.2023.140344. Epub 2023 Oct 4.
Knowledge on the photocatalytic degradability of the emerging poly- and perfluorinated alkyl substances (PFAS) in water, specifically GenX, is limited. GenX has been detected globally in river water and is considered potentially more toxic than legacy PFAS. In this study, we compared the photocatalytic degradability of GenX with the legacy compounds perfluorooctanoic acid (PFOA) and perfluorooctanesulfonic acid (PFOS) using Fe-zeolite photocatalysts. After 7 h of irradiation, GenX showed lower removal (79%) and defluorination (33%) as compared to PFOA (100% removal and 69% defluorination) and PFOS (100% removal and 51% defluorination). The quasi-first-order degradation rate of GenX (1.5 h) was 12 and 1.2 times lower than PFOA (18.4 h) and PFOS (1.8 h), respectively. Additionally, PFOA's defluorination rate (0.9 h) was approximately 2.6 and 9 times higher than GenX (0.35 h) and PFOS (0.1 h), respectively. These outcomes correlate with GenX's lower hydrophobicity, leading to reduced adsorption (40%) compared to PFOA (99%) and PFOS (87%). Based on identified transformation products, we proposed a GenX degradation pathway, resulting in ultra-short-chain PFASs with a chain length of 2 and 3 carbon atoms, while PFOA and PFOS degraded stepwise, losing 1 carbon-fluorine bond at a time, leading to gradually shorter chain lengths (from 7 to 2 carbon atoms). In conclusion, GenX is more challenging to remove and degrade due to its lower adsorption on the photocatalyst, potential steric hindrance, and higher production of persistent ultra-short-chain transformation products through photocatalysis.
关于新兴的多氟和全氟烷基物质(PFAS),特别是GenX在水中的光催化降解性的知识有限。GenX已在全球范围内的河水中被检测到,并且被认为可能比传统的PFAS毒性更大。在本研究中,我们使用铁沸石光催化剂比较了GenX与传统化合物全氟辛酸(PFOA)和全氟辛烷磺酸(PFOS)的光催化降解性。照射7小时后,与PFOA(100%去除和69%脱氟)和PFOS(100%去除和51%脱氟)相比,GenX的去除率(79%)和脱氟率(33%)较低。GenX(1.5小时)的准一级降解速率分别比PFOA(18.4小时)和PFOS(1.8小时)低12倍和1.2倍。此外,PFOA的脱氟速率(0.9小时)分别比GenX(0.35小时)和PFOS(0.1小时)高约2.6倍和9倍。这些结果与GenX较低的疏水性相关,导致其吸附率(40%)低于PFOA(99%)和PFOS(87%)。基于鉴定出的转化产物,我们提出了一条GenX降解途径,生成链长为2和3个碳原子的超短链PFAS,而PFOA和PFOS则逐步降解,每次失去一个碳氟键,导致链长逐渐缩短(从7个碳原子到2个碳原子)。总之,由于GenX在光催化剂上的吸附较低、潜在的空间位阻以及通过光催化产生更多持久性超短链转化产物,其去除和降解更具挑战性。