Du Hu, Wang Xueyao, Zhang Yalan, Xu Guizhou, Tu Yizhou, Jia Xun, Wu Daishe, Xie Xianchuan, Liu Yang
Key Laboratory of Poyang Lake Environment and Resource Utilization, Ministry of Education, School of Resources Environmental & Chemical Engineering, Nanchang University, Nanchang, 330031, China; Nanjing University & Yancheng Academy of Environment Protection Technology and Engineering, Nanjing, 210023, China.
Jiangsu Frontier Electric Technology Co. Ltd, Nanjing, 211102, China; State Key Laboratory of Pollution Control and Resource Reuse, School of the Environment, Nanjing University, Nanjing, 210023, China.
Environ Res. 2022 May 1;207:112160. doi: 10.1016/j.envres.2021.112160. Epub 2021 Sep 30.
The combination of adsorption-photocatalysis and advanced oxidation processes (AOP) based on sulfate (SO) for the treatment of organic pollution has the advantages of a high degradation rate, affordability, and an absence of secondary pollution. This study combined amphiphilic super-crosslinked porous cyclodextrin resin (PBCD-B-D), bismuth oxybromide (BiOBr), a composite material with dual functions of adsorption and photocatalysis, and AOP based on SO for the treatment of Acid Orange 7 (AO7) in water. The combination of BiOBr/PBCD-B-D (BOP-24) with peroxymonosulfate (PMS) showed an optimal adsorption-photocatalytic effect. Compared to the 24% PBCD-B-D (BOP-24)/visible light system, the degradation efficiency of BOP-24/PMS system for AO7 is increased from 64.1% to 99.2% within shorter time (∼60 min). Moreover, the BOP-24/PMS system showed a wide range of pH application (pH = 3-11). The addition of Cl, SO, and NO promoted the photodegradation of AO7, whereas the addition of CO did not. The free radical capture experiments of the BOP-24/PMS AO7 degradation system showed that •O, h, •OH, and SO are reactive species. The proposed BOP-24 system used adsorption and a unique cavity structure to enrich AO7 near the active site, thereby reducing the path for PMS activation. PMS also acted as an electron (e) acceptor to promote the transfer of part of e to PMS, thereby further improving the efficiency of carrier separation. The proposed system is an effective method to improve the degradation of pollutants and broadens the range of application of SO-based AOP technology.
基于硫酸根(SO)的吸附 - 光催化与高级氧化工艺(AOP)相结合用于处理有机污染具有降解速率高、成本低且无二次污染的优点。本研究将两亲性超交联多孔环糊精树脂(PBCD - B - D)、具有吸附和光催化双重功能的复合材料溴氧化铋(BiOBr)与基于SO的AOP相结合,用于处理水中的酸性橙7(AO7)。BiOBr/PBCD - B - D(BOP - 24)与过一硫酸盐(PMS)的组合表现出最佳的吸附 - 光催化效果。与24% PBCD - B - D(BOP - 24)/可见光体系相比,BOP - 24/PMS体系对AO7的降解效率在更短时间(约60分钟)内从64.1%提高到了99.2%。此外,BOP - 24/PMS体系显示出较宽的pH适用范围(pH = 3 - 11)。Cl、SO和NO的添加促进了AO7的光降解,而CO的添加则没有。BOP - 24/PMS AO7降解体系的自由基捕获实验表明,•O、h、•OH和SO是活性物种。所提出的BOP - 24体系利用吸附和独特的空腔结构在活性位点附近富集AO7,从而减少了PMS活化的路径。PMS还作为电子(e)受体促进部分e向PMS的转移,从而进一步提高了载流子分离效率。所提出的体系是提高污染物降解的有效方法,拓宽了基于SO的AOP技术的应用范围。