Biochar co-doped with nitrogen and boron switching the free radical based peroxydisulfate activation into the electron-transfer dominated nonradical process

被引:303
作者
Dou, Jibo [1 ,2 ]
Cheng, Jie [1 ,2 ]
Lu, Zhijiang [3 ]
Tian, Ziqi [4 ]
Xu, Jianming [1 ,2 ]
He, Yan [1 ,2 ]
机构
[1] Zhejiang Univ, Inst Soil & Water Resources & Environm Sci, Coll Environm & Resource Sci, Hangzhou 310058, Peoples R China
[2] Zhejiang Prov Key Lab Agr Resources & Environm, Hangzhou 310058, Peoples R China
[3] Wayne State Univ, Dept Environm Sci & Geol, Detroit, MI 48201 USA
[4] Chinese Acad Sci, Ningbo Inst Mat Technol & Engn, Ningbo 315201, Peoples R China
基金
中国国家自然科学基金;
关键词
Biochar; Heteroatoms doping; Peroxydisulfate activation; Electron transfer; Theoretical calculations; REDUCED GRAPHENE OXIDE; PEROXYMONOSULFATE ACTIVATION; PERSULFATE ACTIVATION; CATALYTIC-OXIDATION; CARBON NANOTUBES; DEGRADATION; TETRACYCLINE; WATER; PERFORMANCE; EFFICIENCY;
D O I
10.1016/j.apcatb.2021.120832
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
In this study, N/B co-doped biochars were employed as metal-free activators of peroxydisulfate (PDS) for tetracycline degradation, more importantly, the roles of dopants and the relative contribution of radical vs nonradical oxidations were comprehensively investigated. Integrating with electron paramagnetic resonance and kinetics calculations, we showed that co-doping N and B into biochars not only boosted the catalytic activity but also switched the radical PDS-activated process into the electron transfer-dominated nonradical process. Compared with pristine biochar/PDS systems (22%), the nonradical contribution of N/B co-doped biochar/PDS systems increased to 59%, exhibiting outstanding stability and selectivity. Galvanic oxidation tests and theoretical simulations unveiled that doped biochars as conductive tunnels accelerate the potential difference-driven electron transfer from the highest occupied molecular orbital of pollutants to the lowest unoccupied molecular orbital of PDS due to the lower energy gap. This study provided new insights into the critical role of heteroatom-doped carbocatalysts in PDS nonradical activation.
引用
收藏
页数:12
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