电负性
催化作用
兴奋剂
金属
化学
过渡金属
污染物
电子转移
降级(电信)
苯
无机化学
化学工程
材料科学
光化学
光电子学
有机化学
计算机科学
电信
工程类
作者
Zhan Gao,Zhiqun Xie,Meiqiang Cai,Chunying Dong,Mengting Weng,Micong Jin,Zongsu Wei
标识
DOI:10.1016/j.cej.2024.153950
摘要
Developing low-cost, sustainable catalysts is critical to meet the green-transition goal in water treatments. Herein, a low-cost, common metal modified g-C3N4 material (FeMg-O-g-C3N4) was designed to improve electron mobility and peroxymonosulfate (PMS) utilization. Likewise, surface acidification of g-C3N4 has introduced extra porous structure, anchor sites for metals, and activate sites. This new catalyst free of expensive rare-earth metals creates numerous surface micro-electric fields through: 1) large difference in electronegativity for Fe (1.83) and Mg (1.31); 2) cation-π effect formed between metals and benzene-like ring structure of g-C3N4; and 3) added PMS and pollutant (tetracycline (TC)) as electron provider promoting the transfer of electrons to the electron-rich Fe sites. Both non-radical (1O2) and radical (surface-bound ·OH and SO4·−) pathways contribute to the pollutant degradation. Given the promising results and stability of the catalyst, this study opens new horizons to apply common metals over expensive, toxic rare metals in PMS-based water treatments.
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