Boron carbide boosted Fenton-like oxidation: A novel Fe(III)/Fe(II) circulation

被引:43
|
作者
Zhou, Peng [1 ,2 ]
Cheng, Feng [1 ]
Nie, Gang [2 ]
Yang, Yangyang [2 ]
Hu, Kunsheng [2 ]
Duan, Xiaoguang [2 ]
Zhang, Yongli [1 ]
Wang, Shaobin [2 ]
机构
[1] Sichuan Univ, Coll Architecture & Environm, Chengdu 610065, Peoples R China
[2] Univ Adelaide, Sch Chem Engn & Adv Mat, Adelaide, SA 5005, Australia
关键词
Boron carbide; Fenton-like reaction; Hydroxyl radical; Metal-free catalysis; Sulfamethoxazole; HYDROXYL RADICALS; ORGANIC POLLUTANTS; HYDROGEN-PEROXIDE; AQUEOUS-SOLUTION; ATOM TRANSFER; DEGRADATION; OXYGEN; ACID; IRON; FE(IV);
D O I
10.1016/j.gee.2020.09.007
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The sluggish kinetics of Fe(II) recovery in Fenton/Fenton-like reactions significantly limits the oxidation efficiency. In this study, we for the first time use boron carbide (BC) as a green and stable promotor to enhance the reaction of Fe(III)/H2O2 for degradation of diverse organic pollutants. Electron paramagnetic resonance analysis and chemical quenching/capturing experiments demonstrate that hydroxyl radicals ((OH)-O-center dot) are the primary reactive species in the BC/Fe(III)/H2O2 system. In situ electrochemical analysis indicates that BC remarkably boosts the Fe(III)/Fe(II) redox cycles, where the adsorbed Fe(III) cations were transformed to more active Fe(III) species with a higher oxidative potential to react with H2O2 to produce Fe(II). Thus, the recovery of Fe(II) from Fe(III) is facilitated over BC surface, which enhances (OH)-O-center dot generation via Fenton reactions. Moreover, BC exhibits outstanding reusability and stability in successive cycles and avoids the secondary pollution caused by conventional organic and metalliferous promotors. Therefore, metal-free BC boosting Fe(III)/H2O2 oxidation of organics provides a green and advanced strategy for water decontamination. (C) 2020, Institute of Process Engineering, Chinese Academy of Sciences. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd. This is an open access article under the CC BY-NC-ND license
引用
收藏
页码:414 / 422
页数:9
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