Highly efficient activation of peroxymonosulfate by cobalt sulfide hollow nanospheres for fast ciprofloxacin degradation

硫化钴 催化作用 降级(电信) 化学 硫化物 罗丹明B 核化学 亚甲蓝 磷酸盐 无机化学 光催化 有机化学 计算机科学 电化学 物理化学 电信 电极
作者
Wenqian Li,Siqi Li,Yue Tang,Xinlu Yang,Wenxuan Zhang,Xiaodan Zhang,Hongxiang Chai,Yuming Huang
出处
期刊:Journal of Hazardous Materials [Elsevier]
卷期号:389: 121856-121856 被引量:189
标识
DOI:10.1016/j.jhazmat.2019.121856
摘要

We reported a facile preparation of CoS2, Co3S4, and Co9S8 hollow nanospheres (HNSs) and their use as peroxymonosulfate (PMS) activators for ciprofloxacin (CIP) degradation. The CIP degradation efficiency follows the order of CoS2 > Co3S4 > Co9S8. The Co2+ is proved to be active site for PMS activation and reactive oxygen species generation. The effect of operating parameters on performance of CoS2 HNSs/PMS system was explored. CoS2 HNSs exhibited highly catalytic activity in a wide pH range of 3 – 10. Complete removal of 10 mg/L CIP was achieved by CoS2 HNSs in 3 min at initial pH of 8.0 with 62.6% CIP mineralization. Three other organic pollutants (rhodamine B, methylene blue and tetracycline) were also degraded to evaluate the universality of the CoS2 HNSs/PMS system. The catalytic performance dropped in the presence of chloride, phosphate, nitrate ions and humic acid. Above 97% CIP removal was achieved even in the sixth run. The degradation pathway of CIP was proposed based on HPLC–MS/MS analysis of CIP intermediates, and two new intermediates, namely, C15H18O4N3F (m/z 323) and C29H31O4N6F (m/z 546), were identified for the first time. Both OH and SO4− were generated and the latter played a key role in CIP degradation.
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