Catalytic oxidation of clofibric acid by peroxydisulfate activated with wood-based biochar: Effect of biochar pyrolysis temperature, performance and mechanism

被引:174
作者
Zhu, Kangmeng [1 ]
Wang, Xisong [1 ]
Geng, Mengzi [1 ]
Chen, Dong [1 ]
Lin, Heng [1 ]
Zhang, Hui [1 ]
机构
[1] Wuhan Univ, Dept Environm Sci & Engn, Hubei Biomass Resource Chem & Environm Biotechnol, Wuhan 430079, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
Wood-based biochar; Pyrolysis temperature; Peroxydisulfate activation; Clofibric acid; Reaction mechanism; PERSISTENT FREE-RADICALS; BISPHENOL-A; AQUEOUS-SOLUTION; ORGANIC CONTAMINANTS; CARBON NANOTUBES; ORANGE; 7; PEROXYMONOSULFATE ACTIVATION; HETEROGENEOUS CATALYSIS; COMPLETE DEGRADATION; HEATED PERSULFATE;
D O I
10.1016/j.cej.2019.06.006
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Wood-based biochars were fabricated at different pyrolysis temperatures of 400-700 degrees C and used to activate peroxydisulfate (PDS) for the degradation of clofibric acid (CA). Biochar pyrolyzed at 700 degrees 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 pi-pi* 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.
引用
收藏
页码:1253 / 1263
页数:11
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