掺杂剂
化学
降级(电信)
光催化
氧气
激进的
磺酸
离解(化学)
氮化硼
光化学
无机化学
有机化学
催化作用
材料科学
兴奋剂
计算机科学
电信
光电子学
作者
Lijie Duan,Jian Wei,Jian Wei,Jinshan Wei,Jinshan Wei,Minghao Wang,Yong Wang,Xue Cheng,Mengbin Gu,Xinyi Zhang,Xianghua Wen,Yonghui Song
标识
DOI:10.1016/j.jhazmat.2022.130419
摘要
6:2 Fluorotelomer sulfonic acid (6:2 FTS) has been identified as an alternative to perfluorooctane sulfonic acid but has been proven to cause potential threats to humans and the environment. In this study, boron nitride (BN) photocatalysis was explored for 6:2 FTS degradation with 100% removal (kobs=1.8 h−1) and desulfurization rate of 100% as well as the defluorination rate of 57.3%. The superior performance of BN was primarily related to oxygen dopants defects (O-dopants). In addition, O-dopants contribution was confirmed by ball-milled BN (B-BN), which introduced more O-dopants and exhibited an increased 6:2 FTS degradation rate of 2.88 h−1. The decomposition of 6:2 FTS was attributed to holes (h+), hydroxyl radicals (•OH), and superoxide (•O2-) and proceeded via two pathways, the hydrogen abstraction from ethyl carbons by •OH and the C-S bond activation by h+ and •OH. To the best of our knowledge, this is the first study demonstrating that h+, •OH, and •O2- played significant roles in the heterogeneous photocatalytic degradation of 6:2 FTS.
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