Synthesis of phosphotungstic acid-supported bimodal mesoporous silica-based catalyst for defluorination of aqueous perfluorooctanoic acid under vacuum UV irradiation

被引:34
作者
You, Xia [1 ]
Yu, Lin-ling [1 ]
Xiao, Fang-fang [1 ]
Wu, Shi-chuan [1 ]
Yang, Cao [1 ]
Cheng, Jian-hua [1 ,2 ]
机构
[1] South China Univ Technol, Guangzhou Higher Educ Mega Ctr, Key Lab Pollut Control & Ecosyst Restorat Ind Clu, Sch Environm & Energy,Minist Educ, Guangzhou 510006, Guangdong, Peoples R China
[2] South China Inst Collaborat Innovat, Dongguan 523808, Peoples R China
关键词
Bimodal mesoporous silica; Phosphotungstic acid; PFOA; VUV irradiation; Defluorination; PERFLUORINATED COMPOUNDS; TITANIUM-DIOXIDE; PHOTOCATALYTIC DECOMPOSITION; PERFLUOROCARBOXYLIC ACIDS; PFOA; WATER; DEGRADATION; SYSTEM; LIGHT; PHOTODEGRADATION;
D O I
10.1016/j.cej.2017.10.123
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Phosphotungstic acid (H3PW12O40, HPW)/bimodal mesoporous silica (BMS) multifunctional catalysts were prepared and employed as photocatalyst for perfluorooctanoic acid (PFOA) degradation under vacuum ultraviolet light (VUV). Lower PFOA concentration, appropriate HPW/BMS dosage (0.2 g center dot L-1) and acidic condition (pH = 3-4) were more favorable for PFOA defluorination in VUV/HPW/BMS system. Furthermore, we analyzed the intermediates produced during PFOA decomposition by HPLC/MS/MS, which were shorter-chain perfluorinated carboxylic acids (PFCAs) with C-7, C-6, C-5, C-4, C-3 and C-2. The defluorination mechanism of PFOA was proposed, i.e., direct photolysis played an important role in PFOA defluorination under VUV radiation (lambda = 185 nm), while the defluorination of PFOA was simultaneously photocatalytically decomposed and defluorinated in the presence of HPW/BMS (lambda = 254 nm).
引用
收藏
页码:812 / 821
页数:10
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