生物炭
过氧二硫酸盐
化学
热解
激进的
氯维甲酸
催化作用
电子顺磁共振
降级(电信)
光化学
猝灭(荧光)
核化学
无机化学
有机化学
荧光
物理
计算机科学
电信
量子力学
核磁共振
生物化学
作者
Kangmeng Zhu,Xisong Wang,Mengzi Geng,Dong Chen,Heng Lin,Hui Zhang
标识
DOI:10.1016/j.cej.2019.06.006
摘要
Wood-based biochars were fabricated at different pyrolysis temperatures of 400–700 °C and used to activate peroxydisulfate (PDS) for the degradation of clofibric acid (CA). Biochar pyrolyzed at 700 °C (BC700) showed more excellent catalytic performance toward CA removal (97.8% in a 60 min reaction) than other BCs. The BC700/PDS process performed efficiently at initial pH range of 4.0–9.0. The effects of PDS concentration and BC700 dosage on CA removal were also examined. Radical quenching experiments and electron paramagnetic resonance (EPR) spectra were applied to identify the reactive radicals generated in the BC700/PDS system. The role of persistent free radicals (PFRs), oxygen functional groups and π-π* transitions in aromatic rings of BC700 for the PDS activation was explored. The reaction intermediates of CA were identified by liquid chromatography–mass spectrometry (LC–MS) and the corresponding degradation pathway was proposed. This study contributes to the development of green materials for sustainable remediation of organic contaminants in water and provides support for further studies.
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