Highly-efficient degradation of triclosan attributed to peroxymonosulfate activation by heterogeneous catalyst g-C3N4/MnFe2O4

被引:82
作者
Wang, Jing [1 ]
Yue, Min [1 ]
Han, Yuze [2 ]
Xu, Xing [1 ]
Yue, Qinyan [1 ]
Xu, Shiping [1 ]
机构
[1] Shandong Univ, Sch Environm Sci & Engn, Shandong Key Lab Water Pollut Control & Resource, 27 Shanda South Rd, Jinan 250100, Peoples R China
[2] Nanjing Univ, Sch Environm, 163 Xianlin Ave, Nanjing 210023, Peoples R China
关键词
Peroxymonosulfate; g-C3N4/MnFe2O4; Triclosan; Degradation; Reaction parameters; Intermediates; RADICALS INDUCED DEGRADATION; SULFATE RADICALS; PHOTOCATALYTIC ACTIVITY; ORGANIC CONTAMINANTS; PHENOLIC-COMPOUNDS; BISPHENOL-A; PERFORMANCE; GRAPHENE; REMOVAL; WATER;
D O I
10.1016/j.cej.2019.123554
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The g-C3N4/MnFe2O4 as recyclable catalyst was synthesized via auto-combustion sol-gel method. Peroxymonosulfate (PMS) activation by the catalyst for triclosan (TCS) degradation was investigated considering the activation performance, reaction parameters and activation mechanism. The catalyst prepared with 1:1 of g-C3N4 and MnFe2O4 molar ratio performed the best catalytic activity in the TCS degradation and with lest metal leaching. The concentration of Cl- showed a dual effect on the TCS degradation, while HCO3- and SO42- performed inhibitory effect. Sulfate radicals, hydroxyl radicals, superoxide and non-radical single oxygen contributed to the degradation of TCS. Compared with MnFe2O4/PMS system, few heavy metals were leached from g-C3N4/MnFe2O4(1:1)-PMS after each reuse (Fig. S6b), suggesting that g-C3N4 was conducive to the stability of g-C3N4/MnFe2O4(1:1) catalyst. Dichlorination, hydroxylation, cyclization and other bond breaking reaction were inferred as the TCS degradation pathways. These results demonstrated that g-C3N4/MnFe2O4(1:1) was a highly effective and stable catalyst for PMS activation to treat toxic organic pollutants in water.
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页数:13
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