罗丹明B
化学
催化作用
水溶液
降级(电信)
核化学
过氧二硫酸盐
钴
热液循环
污染物
无机化学
光化学
化学工程
光催化
有机化学
计算机科学
电信
工程类
作者
Qin Yang,Yujie Zhang,Jie Liang,Yongsong Luo,Qian Liu,Yingchun Yang,Xuping Sun
标识
DOI:10.1016/j.colsurfa.2022.129239
摘要
Sulfate radical based advanced oxidation processes (SR-AOPs) are regarded as a promising technology to degrade organic pollutants in water. Here, hydrothermally synthesized Co-glycerate (Co-G) microspheres are proposed as an efficient heterogeneous catalyst to activate peroxymonosulfate (PMS) for degradation of refractory organic pollutant rhodamine B (RhB) in aqueous solution. The presence of Co-G microspheres enhanced the degradation rate significantly with a short full degradation time (8 min) and a total organic carbon (TOC) removal exceeding 41% (10 min), thus implying the excellent catalytic performance of Co-G microspheres for PMS activation. Furthermore, the effects of PMS and catalyst concentration, initial pH value and co-existing ions on RhB degradation were investigated. Radical quenching and EPR tests identify that active species including SO 4 - ·, HO·, O 2 - · and 1 O 2 are involved in the degradation process. Additionally, a possible reaction mechanism of PMS activation by Co-G microspheres for RhB degradation was suggested. This study can provide a new insight for design of cobalt-based heterogeneous catalysts as activators to activation PMS for pollutants degradation. Co-glycerate (Co-G) microspheres were used as efficient catalyst to activate peroxymonosulfate (PMS) for degradation of refractory organic pollutant rhodamine B (RhB) in aqueous solution. In 50 mg/L RhB solution (100 mL) containing 0.05 g/L PMS and 0.02 g/L Co-G, RhB is completely degraded with a short degradation time (8 min), and the removal of total organic carbon (TOC) exceed 41% within 10 min
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