双酚A
催化作用
MXenes公司
化学
动力学
反应机理
机制(生物学)
化学工程
化学动力学
有机化学
量子力学
认识论
物理
工程类
哲学
环氧树脂
作者
Fei Wang,Yuxian Lai,Qinglu Fang,Zhiying Li,Ping Ou,Panpan Wu,Yaxiao Duan,Zhuang Chen,Shuai Li,Yimei Zhang
标识
DOI:10.1016/j.apcatb.2019.118099
摘要
Herein, a novel of Co(OH)[email protected] nanomaterials with unique structure as the catalyst for activating peroxymonosulfate (PMS) to degrade bisphenol A (BPA) is reported. The properties of as-prepared catalyst were tested by diverse of characterization techniques. Importantly, the Co(OH)[email protected] activates PMS to degrade BPA more efficiently (96.3% within 40 min) and stably than traditionally Co3O4 and CoO nanomaterials. Different influence factors of BPA degradation were also examined, including different catalyst, pH, temperature, BPA concentrations, PMS dosage, catalyst dosage and co-existing ions. The existence of Cl− and H2PO4− exhibit distinct positive synergistic effects on the catalytic process. The XPS and ICP techniques were applied to illustrate that the leach amount of cobalt ion was very litter. Thus, the reusable ability of Co(OH)[email protected] without significant efficiency loss after multiple cycles. These results demonstrate that Co(OH)[email protected] is an promisingly effective catalyst to activating PMS for BPA remove.
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