Cao Xin, Ding Li, Peng Jianbiao, Wang Weilai, Zhang Yakun, Chang Yu, Wang Tian, Soltan Wissem Ben, Cao Zhiguo, Liu Haijin
School of Environment, Henan Normal University, Key Laboratory for Yellow River and Huaihe River Water Environment and Pollution Control, Ministry of Education, Henan Key Laboratory for Environmental Pollution Control, Xinxiang 453007, PR China.
School of Environment, Henan Normal University, Key Laboratory for Yellow River and Huaihe River Water Environment and Pollution Control, Ministry of Education, Henan Key Laboratory for Environmental Pollution Control, Xinxiang 453007, PR China; School of Water Resources and Environmental Engineering, Nanyang Normal University, Nanyang 473061, PR China.
Sci Total Environ. 2024 Nov 15;951:175492. doi: 10.1016/j.scitotenv.2024.175492. Epub 2024 Aug 13.
In recent years, the academic community has shown significant interest in per- or polyfluoroalkyl compounds (PFAS) due to their challenging degradation and potential health risks. Photocatalysis has been investigated for PFAS decomposition due to its environmentally friendly nature. In this study, BiOI with abundant iodine vacancies was synthesized through solvothermal and calcination methods (referred to as BiOI), and was used for PFAS degradation with a low power UV light source. Compared to pure BiOI, BIOI showed higher photocatalytic activity towards PFOA (perfluorooctanoic acid). Within 5 h under 5 W LED light irradiation, the degradation rate of PFOA reached 51.9 % with BiOI calcined at 440 °C (No significant degradation of PFAS was observed with pure BiOI). Capture experiments, electron paramagnetic resonance spectroscopy, and electrochemical experiments revealed that the main active species in the system were photogenerated holes, followed by hydroxyl radicals. Furthermore, the presence of iodine vacancies significantly improved the efficiency of charge carrier separation and enhanced the photocatalytic performance. Finally, a hypothetical degradation pathway for PFOA in this system was suggested. This study achieved efficient degradation of PFAS under low power LED light (5 W), emphasizing its significant practical importance in terms of energy conservation.
近年来,由于全氟或多氟烷基化合物(PFAS)难以降解且存在潜在健康风险,学术界对其表现出了极大的兴趣。光催化因其环境友好的特性而被用于研究PFAS的分解。在本研究中,通过溶剂热法和煅烧法合成了具有大量碘空位的BiOI(简称BiOI),并将其用于低功率紫外光源下的PFAS降解。与纯BiOI相比,BIOI对全氟辛酸(PFOA)表现出更高的光催化活性。在5W LED光照射下5小时内,440℃煅烧的BiOI对PFOA的降解率达到51.9%(纯BiOI未观察到PFAS的显著降解)。捕获实验、电子顺磁共振光谱和电化学实验表明,体系中的主要活性物种是光生空穴,其次是羟基自由基。此外,碘空位的存在显著提高了载流子分离效率,增强了光催化性能。最后,提出了该体系中PFOA的假设降解途径。本研究实现了低功率LED光(5W)下PFAS的高效降解,强调了其在节能方面的重要实际意义。