4.7 Article

High efficient activation of peroxymonosulfate by Co9S8 anchored in N, S, O co-doped carbon composite for degradation of sulfamethoxazole: Effect of sulfur precursor and sulfur doping content

期刊

CHEMICAL ENGINEERING JOURNAL
卷 434, 期 -, 页码 -

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2022.134824

关键词

Cobalt sulfides; Persulfate; Antibiotics; Catalytic activity

资金

  1. National Natural Science of China
  2. Program for Changjiang Scholars and Innovative Research Team in University

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Cobalt sulfides as persulfate activator have been studied for their catalytic activity in persulfate-based advanced oxidation process. This study successfully prepared Co9S8 anchored in N, S, O heteroatoms co-doped carbon composite, which showed high catalytic activity in activating peroxymonosulfate for sulfamethoxazole degradation. The study also investigated the effect of various factors on the degradation process and identified the active sites and intermediate products involved.
Cobalt sulfides as persulfate activator have received increasing interest in the field of persulfate-based advanced oxidation process. In this study, Co9S8 anchored in N, S, O heteroatoms co-doped carbon (CoSx@N-S-O-C) composite was prepared with different sulfur precursors (sulfur, thiourea, thiophene and benzyl disulfide), and used to activate peroxymonosulfate (PMS) for sulfamethoxazole (SMX) degradation. The effect of temperature, pH, inorganic ions, humic acids and water components on SMX degradation was investigated. The results showed that sulfur precursor could regulate the catalytic activity of the composite through changing the cobalt speciation and carbon structure. The catalytic activity was highest when the molar ratio of sulfur to cobalt was 5:1 (CoSx@N-S-O-C-5). Sulfate radicals (dominant) and hydroxyl radicals contributed to SMX degradation. The in-termediate products during SMX degradation were identified, and the possible pathway of SMX degradation was proposed. Pyridinic N, Co-N, cobalt, S2- , S-2(2-), C-S-C and C-SOx were active sites for PMS activation.

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