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Enhanced peroxymonosulfate activation by MoS2/NiCo2S4 composite catalyst for efficient elimination of tetracycline hydrochloride

催化作用 化学 单线态氧 激进的 硫化物 盐酸四环素 无机化学 核化学 硫黄 协同催化 氧气 有机化学 四环素 生物化学 抗生素
作者
Chenglin Li,Dedong Sun,Hongchao Ma,Xinxin Zhang,Guowen Wang,Jun Hao
出处
期刊:Journal of environmental chemical engineering [Elsevier BV]
卷期号:12 (1): 111900-111900 被引量:8
标识
DOI:10.1016/j.jece.2024.111900
摘要

Compared to metal oxide, owing to the sulfur's lower electronegativity, metal sulfide is a promising catalyst. Molybdenum disulfide (MoS2) has been used as a catalyst or co-catalyst in the technology of peroxymonosulfate (PMS) activation due to its conductivity and rich active sites. In this work, MoS2/NiCo2S4 composite was synthesized successfully as an effective catalyst to activate PMS for removal of tetracycline hydrochloride (TCH). Catalyst screening indicated the composite with a Mo:Co molar ratio of 0.5:1 (0.5-MoS2/NiCo2S4) exhibited the best PMS activation performance. The results showed that 98.3% of TCH (15 mg/L) was removed, and the removal efficiency of total organic carbon (TOC) was 54.5% within 90 min under conditions of an Oxone dosage of 400 mg/L and a catalyst dosage of 300 mg/L. The main active substances were found to be sulfate radicals (SO4•−), hydroxyl radicals (•OH), superoxide radicals (O2•−) and singlet oxygen (1O2) in 0.5-MoS2/NiCo2S4/PMS system based on the active species quenching tests and electron paramagnetic resonance (EPR) analyses. A potential activation mechanism for the 0.5-MoS2/NiCo2S4/PMS system was proposed in the following two aspects: one is that molybdenum and sulfur species enhanced the cyclic transformation of Co3+/Co2+ and Ni3+/Ni2+ in the reaction system, and the other is the synergy of Co3+/Co2+, Ni3+/Ni2+ and Mo6+/Mo4+ cycles in the PMS activation. In summary, owing to its high activity and reusability, the 0.5-MoS2/NiCo2S4 composite is a promising catalyst for wastewater treatment.
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