Enhanced degradation of bisphenol A over CFO/CMK-3 involved PMS activation: Insights into the synergistic effect between the spinel and mesoporous carbon

被引:7
作者
Peng, Xuezhi [1 ]
Yu, Shihui [1 ]
Chen, Jianjian [1 ]
Yang, Jiaojiao [1 ]
Guo, Binyu [1 ]
Zhou, Juan [1 ,2 ]
机构
[1] Donghua Univ, Coll Environm Sci & Engn, Text Pollut Controlling Engn Ctr, Minist Ecol & Environm, Shanghai 201620, Peoples R China
[2] Shanghai Inst Pollut Control & Ecol Secur, Shanghai 200092, Peoples R China
基金
上海市自然科学基金; 中国国家自然科学基金;
关键词
Bisphenol A; CFO; CMK-3; PMS activation; Surface; -bound; Synergistic effect; CATALYTIC HYDRODECHLORINATION; EFFICIENT DEGRADATION; PEROXYMONOSULFATE; PERSULFATE; OXIDATION; PEROXYDISULFATE; RADICALS;
D O I
10.1016/j.seppur.2022.122861
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Here, we prepared ordered mesoporous carbon (CMK-3) coupled spinel CoFe2O4 (CFO) composite catalyst, in which the CFO nanoparticles were uniformly dispersed on the surface of CMK-3. The catalyst was applied for the elimination of bisphenol A (BPA) involved PMS activation. The removal rate was 96 % for CFO/CMK-3 after reaction for 15 min, much higher than that of single CMK-3 (19 %) and CFO (47 %). The CFO/CMK-3/PMS system can efficiently remove BPA in a wide pH range of 3???11 and strong alkaline conditions (pH 11) facilitated the oxidation reaction due to the vital role of surface-bound active species. Quenching experiments and Electron Paramagnetic Resonance (EPR) signals demonstrated that free ???OH, SO4?????? and 1O2 were involved in the AOPs of BPA, while the surface-bound active species predominated the degradation. The synergistic mechanism between CFO and CMK-3 could be depicted that CFO increased the electron-rich centers of CMK-3. PMS was activated by Co2+/Co3+ and Fe3+/Fe2+ in CFO and electron-rich centers in CMK-3, respectively, then the adsorbed BPA was degraded by adjacent surface-bound and/or free active species. Besides, the composite catalyst could also act as the electron transfer tunnel favoring charges move from adsorbed H2O/OH??? to PMS and resulting in enhanced PMS activation. The coexistent humic acid and NO3??? showed slight depression on the reaction while the presence of HCO3??? and Cl??? facilitated the degradation.
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页数:9
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