X射线光电子能谱
降级(电信)
吸附
催化作用
矿化(土壤科学)
化学工程
极化(电化学)
光致发光
材料科学
苯胺
化学
分析化学(期刊)
物理化学
氮气
环境化学
光电子学
工程类
计算机科学
有机化学
电信
作者
Shuchen Tu,Tianyang Hao,Xiangming Li,Tao Chen,Yaqing Wang,Junhao Zhang,Chengyu Zhou,Linghui Kuang,Peng Xu,Yuan Zeng,Keqing Ouyang,Shaojun Jiang,Bo Yan
出处
期刊:ACS ES&T engineering
[American Chemical Society]
日期:2024-04-08
卷期号:4 (7): 1573-1584
被引量:1
标识
DOI:10.1021/acsestengg.4c00049
摘要
The great ecological hazards of mineral processing wastewater containing aniline aerofloat dictate the need to implement thorough mineralization degradation, such as Fenton-like catalysis. To address the low efficiency of H2O2 conversion and the short reactive duration in Fenton-like aniline aerofloat degradation, in this study, we demonstrated a novel piezo-enhanced mechanism that utilizes piezo-induced macroscopic polarization to significantly enhance H2O2 conversion and Fe3+/Fe2+ cycling in the Fe3O4–Bi4Ti3O12 heterojunction. The reaction activity was increased 2-fold, resulting in the removal of almost 85% of aniline aerofloat within 40 min at a pH of 4–10. The combination of piezoelectric force microscopy, in situ electrochemical measurement, transmission electron microscopy, and X-ray photoelectron spectroscopy demonstrated that Fe3O4–Bi4Ti3O12 exhibited a strong piezo-response and improved charge migration when exposed to a piezo-potential. The piezo-induced large-scale charge transfer facilitated the adsorption of H2O2 and released the kinetic constraints for Fe3+/Fe2+ cycling by inducing charge enrichment, as confirmed by radical monitoring, photoluminescence spectroscopy, and theory calculations. Consequently, the optimization of the aforementioned key processes enhances the yield rate (1.363 μmol min–1), selectivity of HO• conversion (18.88%) by H2O2, and the reaction's persistence. This work presents an innovative concept to enhance the performance and endurance of Fenton-like reactions. It also provided an understanding of the advanced oxidation process treatment of mineral processing wastewater.
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