The degradation of oxytetracycline with low concentration of persulfate sodium motivated by copper sulphate under simulated solar light

被引:32
作者
Bi, Wenlong [1 ]
Wu, Yanlin [2 ]
Dong, Wenbo [2 ]
机构
[1] Shanxi Agr Univ, Coll Resources & Environm, Taigu 030801, Shanxi, Peoples R China
[2] Fudan Univ, Dept Environm Sci & Engn, Shanghai Key Lab Atmospher Particle Pollut & Prev, Shanghai 200433, Peoples R China
关键词
Oxytetracycline; Persulfate sodium; Copper sulfate; Simulated solar light; TETRACYCLINE RESISTANCE GENES; ZERO-VALENT IRON; ACTIVATED PERSULFATE; AQUEOUS-SOLUTION; WASTE-WATER; OXIDATIVE-DEGRADATION; SPECTROPHOTOMETRIC DETERMINATION; ANTIBIOTIC OXYTETRACYCLINE; CHEMICAL OXIDATION; P-CHLOROANILINE;
D O I
10.1016/j.cej.2019.122782
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Degradation of OTC with Cu2+/PS under simulated solar light was investigated. Under simulated solar light or UV-254 light, metal ions could increase the degradation of OTC (< 10%) and the order was that Cu2+ > Mn2+ > Zn2+ > Cr3+ > Mg2+ approximate to Ca2+. When PS was used, the degradation of OTC under simulated solar light improved only with Cu2+. The optimum condition of OTC/Cu-2+/PS under simulated solar light was OTC:Cu2+:PS= 1:1.5:1.75 and the removal rate of OTC could reach 93.5% after 1 h irradiation. In addition, the improvement of degradation of OTC with Cu2+/PS could also be found under UV-254 light or visible light, and the results showed that the energy of light could play an important role in the degradation of OTC. The mechanism of OTC/Cu2+/PS under light was discussed, and it could be that, under light irradiation, Cu2+ could change into Cu+ which could motive PS to produce SO4 center dot-. The degradation of OTC with Cu2+/H2O2 under simulated light was studied to verify the mechanism. Moreover, The mineralization of OTC with Cu2+/PS under simulated solar light was analyzed. Furthermore, seven products were detected by LC-MS (EI+) and the OTC degradation pathway was discussed.
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页数:8
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