生物炭
过硫酸盐
热解
降级(电信)
化学
催化作用
尖晶石
光化学
电子转移
化学工程
氧气
材料科学
有机化学
冶金
工程类
电信
计算机科学
作者
Lin Wang,Xiping Lu,Guodong Chen,Youzheng Zhao,Shaolong Wang
标识
DOI:10.1016/j.cej.2023.143773
摘要
Exploiting environment-friendly and cost-effective catalysts and understanding their catalytic mechanisms are a great challenge in persulfate-based advanced oxidation processes (PS–AOPs). Herein, a simple sol–gel pyrolysis procedure was employed to generate a novel magnesium ferrite/biochar (MgFe2O4/BC), exhibiting excellent degradation abilities to tetracycline (TC) (94.70% within 90 min). Characterization results demonstrated that biochar (BC) increased the dispersibility, surface area, and electronic transfer capability of MgFe2O4. Compared with the single MgFe2O4 and BC, the TC degradation efficiency of the novel MgFe2O4/BC was significantly improved by 78.49% and 45.97%, which ascribed to the synergies causing the composite possessed large specific surface area and exposing more active sites. The quenching test and electron spin resonance revealed the dominance of 1O2 and O2•− among the identified reactive oxygen species. Oxygen vacancy and carbonyl were identified as the main active sites. A possible TC degradation pathway has been proposed, and reduced toxicity of intermediates was observed. This study provides a new perspective on understanding the persulfate activation mechanism by spinel-biochar composites.
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