双酚A
化学
催化作用
电子顺磁共振
分解
降级(电信)
X射线光电子能谱
反应速率常数
激进的
核化学
硫黄
猝灭(荧光)
纳米颗粒
反应机理
动力学
荧光
化学工程
有机化学
工程类
环氧树脂
物理
电信
量子力学
核磁共振
计算机科学
作者
Yaobin Ding,Yue Hu,Xueqin Peng,Yuwen Xiao,Jia Huang
标识
DOI:10.1016/j.seppur.2019.116022
摘要
Co-based catalysts demonstrated high performance for activating peroxymonosulfate (PMS). In the present study, micro-nano structured CoS was prepared by a simple solvothermal reaction and the influence of sulfur in CoS in the PMS activation for bisphenol A (BPA) decomposition was investigated systematically. It was found that micro-nano structured CoS exhibited remarkable catalytic activity with 90% removal of 20 mg L−1 BPA within 10 min under 0.05 g L−1 CoS and 0.3 mmol L−1 PMS at 25 °C. The peso-first reaction rate constant for BPA degradation in this system was 0.37 min−1, 1.1 and 1.5 times that by using surface sulfur modified Co3O4 (S-Co3O4) and Co3O4 nanoparticles as a catalyst. Factors influencing BPA degradation were also examined, including initial pH (pH0), dosages of PMS and CoS. The BPA removal was enhanced with the raise from 3 to 11 in the reaction solution due to enhanced PMS decomposition and free radicals production. Moreover, the conversion of SO4− to OH as the main reactive species was observed as pH0 was varied from 3 to 10 through electron paramagnetic resonance (EPR) analysis and quenching experiments. BPA degradation pathways by CoS/PMS system were proposed based on LC-MS results of degradation intermediates. Finally, a possible mechanism for activation of PMS by CoS was proposed according to the surface evolution of CoS during the reaction process by XPS spectra.
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