Fe, N-doped carbonaceous catalyst activating periodate for micropollutant removal: Significant role of electron transfer

被引:223
作者
He, Lei [1 ]
Yang, Chao [1 ]
Ding, Jie [1 ]
Lu, Mei-Yun [1 ]
Chen, Cheng-Xin [1 ]
Wang, Guang-Yuan [1 ]
Jiang, Jun-Qiu [1 ]
Ding, Lan [2 ]
Liu, Guo-Shuai [3 ]
Ren, Nan-Qi [1 ]
Yang, Shan-Shan [1 ]
机构
[1] Harbin Inst Technol, Sch Environm, State Key Lab Urban Water Resource & Environm, Harbin 150090, Peoples R China
[2] Jilin Univ, Coll Chem, Changchun 130012, Peoples R China
[3] Jiangnan Univ, Sch Environm & Civil Engn, Wuxi 214122, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Coagulation waste; Periodate; Electron transfer; DFT; Sulfadiazine; PHOTOACTIVATED PERIODATE; BIOCHAR; DEGRADATION; OXIDATION; RADICALS; DECOLORIZATION; PERSULFATE; ADSORPTION; MECHANISM; WASTE;
D O I
10.1016/j.apcatb.2021.120880
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, the performance of periodate (PI) on sulfadiazine (SDZ) degradation was evaluated using coagulation solid waste fabricated catalyst (CWBC), obtained by simple pyrolysis. SDZ effectively underwent 98.94% remove within 90 min in the CWBC/PI system. Electron transfer was the predominant mechanism due to the development of an electronic cycle among SDZ, CWBC and PI, where the O-2(center dot-), PFRs, and the reactive iodine species had minor roles. Density functional theory calculations identified that Fe and N could change the electron configuration and break the chemical inertness of carbonaceous material. As a result, electrons on the carbon matrix of CWBC are inclined to travel through the formed Fe-O covalent bond to PI. Further analysis demonstrated that SO42-, humic acid (HA), as well as anoxic conditions greatly facilitated SDZ degradation. This study provides a facile protocol for converting coagulation waste to an efficient catalyst and provides fundamental insights into the degradation mechanisms of micropollutants by activating PI.
引用
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页数:14
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