journal article·2018-11-14

Mechanism of heterogeneous activation of persulfate with FeOCl under visible light irradiation

Mengdie Chen, Haiming Xu, Xiaofang Zhang, Dongya Li, Dongsheng Xia

Journal of Materials Research· Volume 33· Issue 21
Publisher page

Abstract

Activation of persulfate (PS) by ultraviolet light or transition metal catalysts has been extensively studied. However, little is known about the activation of PS by iron oxychloride (FeOCl) in the presence of visible light irradiation. Herein, the catalytic activity of FeOCl was developed for oxidative degradation of rhodamine B (RhB) with the FeOCl/PS/Vis process. The characterization of FeOCl for reaction kinetics, degradation mechanism, and catalyst stability was investigated. It is found that the redox cycle of iron species and photoinduced electrons formed on the FeOCl catalyst surface can effectively activate PS, to generate radicals. Based on quenching experiments and electron paramagnetic resonance, the photogenerated holes (h+) and sulfate radicals (SO4−•) are the predominant reactive oxidants for RhB decolorization, while superoxide radicals (•O2−) and hydroxyl radicals (•OH) are also involved. Moreover, FeOCl shows good catalytic performance in a wide range of pH values (pH = 3–10) and excellent reusability and stability, as well.
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Research context

OpenAlex topics: Advanced Photocatalysis Techniques · Advanced oxidation water treatment · Electrochemical Analysis and Applications

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References (43)

Show source-provided references
1. 10.1016/j.apsusc.2006.05.02310.1016/j.apsusc.2006.05.023 ↗
2. 10.1021/la904023j10.1021/la904023j ↗
3. 10.1016/j.apcatb.2014.01.03110.1016/j.apcatb.2014.01.031 ↗
4. 10.1021/ja409130c10.1021/ja409130c ↗
5. 10.1002/aoc.420910.1002/aoc.4209 ↗
6. 10.1016/j.jallcom.2016.06.00410.1016/j.jallcom.2016.06.004 ↗
7. 10.1016/j.apcatb.2016.12.00110.1016/j.apcatb.2016.12.001 ↗
8. 10.1016/j.seppur.2011.06.02310.1016/j.seppur.2011.06.023 ↗
9. 10.1016/j.apcatb.2008.07.01010.1016/j.apcatb.2008.07.010 ↗
10. 10.1021/ie504111y10.1021/ie504111y ↗
11. 10.1016/j.cej.2010.10.01810.1016/j.cej.2010.10.018 ↗
12. 10.1002/chem.20160017210.1002/chem.201600172 ↗
13. 10.1021/ie503437z10.1021/ie503437z ↗
14. 10.1021/la100302m10.1021/la100302m ↗
15. 10.1021/ja00141a01510.1021/ja00141a015 ↗
16. 10.1016/j.watres.2009.09.05510.1016/j.watres.2009.09.055 ↗
17. 10.1016/j.apsusc.2014.10.16110.1016/j.apsusc.2014.10.161 ↗
18. 10.1007/s12274-014-0416-010.1007/s12274-014-0416-0 ↗
19. 10.1021/es050634b10.1021/es050634b ↗
20. 10.1039/C6RA18391C10.1039/C6RA18391C ↗
21. 10.1016/j.apcatb.2015.12.00210.1016/j.apcatb.2015.12.002 ↗
22. 10.1007/s11356-016-8020-310.1007/s11356-016-8020-3 ↗
23. 10.1080/71361097010.1080/713610970 ↗
24. 10.1016/j.jcat.2004.08.00310.1016/j.jcat.2004.08.003 ↗
25. 10.1021/es503741d10.1021/es503741d ↗
26. 10.1016/j.apcatb.2015.03.00110.1016/j.apcatb.2015.03.001 ↗
27. 10.1002/admi.20150080110.1002/admi.201500801 ↗
28. 10.1002/sia.198410.1002/sia.1984 ↗
29. 10.1016/S0926-3373(98)00019-810.1016/S0926-3373(98)00019-8 ↗
30. 10.1016/j.chemosphere.2016.01.00210.1016/j.chemosphere.2016.01.002 ↗
31. 10.1016/j.seppur.2011.06.02110.1016/j.seppur.2011.06.021 ↗
32. 10.1016/j.apcatb.2003.12.01810.1016/j.apcatb.2003.12.018 ↗
33. 10.1016/j.apcatb.2015.03.05310.1016/j.apcatb.2015.03.053 ↗
34. 10.1103/PhysRevB.82.16512110.1103/PhysRevB.82.165121 ↗
35. 10.1016/j.apcatb.2016.09.00510.1016/j.apcatb.2016.09.005 ↗
36. 10.1039/c4ra02735c10.1039/c4ra02735c ↗
37. 10.1021/acs.est.5b0597410.1021/acs.est.5b05974 ↗
38. 10.1016/j.seppur.2016.03.02610.1016/j.seppur.2016.03.026 ↗
39. 10.1021/es061395a10.1021/es061395a ↗
40. 10.1016/j.apcatb.2007.07.02010.1016/j.apcatb.2007.07.020 ↗
41. 10.1016/j.chemosphere.2013.12.03710.1016/j.chemosphere.2013.12.037 ↗
42. 10.1016/S0891-5849(87)80033-310.1016/S0891-5849(87)80033-3 ↗
43. 10.1039/c2jm34778d10.1039/c2jm34778d ↗