双酚A
过硫酸盐
化学
过氧二硫酸盐
氧化铈
催化作用
降级(电信)
铈
激进的
钯
溴
核化学
单线态氧
环境化学
无机化学
氧气
有机化学
电信
计算机科学
环氧树脂
作者
Alexandra Α. Ioannidi,Georgios Bampos,Μαρία Αντωνοπούλου,Paula Oulego,Dionissios Mantzavinos,Zacharias Frontistis
标识
DOI:10.1016/j.jece.2023.111851
摘要
In this study, a series of Pd/CeO2 catalysts were synthesized, characterized, and evaluated for the activation of persulfate and the degradation of the micropollutant, bisphenol A (BPA). The efficiency followed a volcano-type behavior with respect to Pd loading, and the 0.25% wt. Pd/CeO2 exhibited the highest catalytic activity. However, this activity strongly depended on the operating conditions. The system was able to degrade 500 μg/L BPA in less than 30 min, and the removal was favored at near neutral pH (6.2). Scavenging experiments highlighted the role of superoxide and singlet oxygen, followed by sulfate radicals. The efficiency was found to be stable across several cycles, despite a slight decrease in the first cycle. The removal of BPA decreased with the complexity of the water matrices, showing the need for system optimization under real conditions. Five transformation products were identified using UHPLC-TOF-MS and their ecotoxicity was estimated using ECOSAR. Intriguingly, the system was capable of inactivating 99.99% of 2.4 ×105 CFU/mL E. coli, in less than 210 min making it an appealing alternative technology for the simultaneous inactivation of pathogens and degradation of micropollutants in environmental systems.
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