Nitrogen, sulfur and oxygen co-doped carbon-armored Co/Co9S8 rods (Co/Co9S8@N-S-O-C) as efficient activator of peroxymonosulfate for sulfamethoxazole degradation

硫黄 硫化钴 化学 氮气 降级(电信) 催化作用 激进的 无机化学 腐植酸 矿化(土壤科学) 反应速率常数 核化学 动力学 有机化学 肥料 电化学 物理化学 物理 电信 量子力学 计算机科学 电极
作者
Shizong Wang,Haiyang Liu,Jianlong Wang
出处
期刊:Journal of Hazardous Materials [Elsevier BV]
卷期号:387: 121669-121669 被引量:75
标识
DOI:10.1016/j.jhazmat.2019.121669
摘要

In this study, nitrogen, sulfur and oxygen co-doped carbon armored cobalt sulfide (Co/Co9S8@N-S-O-C) composite was synthesized, characterized and used to activate peroxymonosulfate (PMS) for the degradation of sulfamethoxazole (SMX). SMX (0.04 mM) can be completely degraded within 20 min in the presence of 0.8 mM PMS and 0.1 g/L Co/Co9S8@N-S-O-C composite. The first-order kinetics constant of SMX degradation was 0.307 min-1, and the mineralization of SMX was 30.1 %. The Quenching experiments of the free radicals and the identification of degradation products demonstrated that sulfate radicals played a dominant role in SMX degradation. The degradation rate of SMX increased with temperature, and activation energy was calculated to be 48.6 kJ/mol. The degradation rate of SMX increased firstly then decreased with increase of pH. Chloridion and humic acid decreased the degradation rate of SMX no matter what their initial concentration was. The effect of carbonate on SMX degradation depended on its initial concentration. Co/Co9S8@N-S-O-C composite showed good stability, the removal efficiency of SMX was 98.4 % in the fifth experiment. Based on the characterization results of the catalyst before and after use, it was concluded that cobalt, sulfur, pyridnic N and graphitic N were responsible for PMS activation.
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