Activation of sulfite by single-atom Fe deposited graphitic carbon nitride for diclofenac removal: The synergetic effect of transition metal and photocatalysis

被引:102
作者
Zhao, Zhiwei [1 ]
Zhang, Wei [1 ]
Liu, Wen [2 ,3 ]
Li, Yunyi [1 ]
Ye, Jiangyu [1 ]
Liang, Jialiang [1 ]
Tong, Meiping [2 ]
机构
[1] Chongqing Univ, Minist Educ, Key Lab Three Gorges Reservoir Reg Ecoenvironm, Chongqing 400044, Peoples R China
[2] Peking Univ, Coll Environm Sci & Engn, Minist Educ, Key Lab Water & Sediment Sci, Beijing 100871, Peoples R China
[3] Peking Univ, Beijing Innovat Ctr Engn Sci & Adv Technol BIC ES, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
Sulfite activation; Ultra-small Fe dusters; g-C3N4; Diclofenac; ADVANCED OXIDATION PROCESS; ORGANIC POLLUTANTS; RATE CONSTANTS; DEGRADATION PATHWAYS; WASTE-WATER; KINETICS; SYSTEM; PERSULFATE; TOXICITY; DRIVEN;
D O I
10.1016/j.cej.2020.127167
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Herein, through supramolecular gel assisted pre-configuration, a novel bamboo-like porous graphitic carbon nitride (g-C3N4) deposited with single-atom Fe was successfully prepared and used for sulfite (S(IV)) activation. Unexpectedly, owing to the presence of single-atom Fe, hybrid material with only 2.5 parts per thousand of Fe exhibited 16 times higher S(IV) activation efficiency for diclofenac removal than pure g-C3N4 under visible light irradiation. Moreover, a synergetic effect of Fe and g-C3N4 was found to play the dominate role, and the synergetic factor was calculated to be 0.84. The synergetic mechanism mainly related to the generation of surface Fe-S(IV) complex, which could be affected by S(IV) species or the presence of H2PO4-. DCF removal was significantly enhanced at alkaline condition, but the enhancement was mainly attributed to photocatalysis but not synergetic effect. Decarboxylation, hydroxylation, chlorine abstraction and cleavages at bridging N atom were the main degradation pathways of DCF, which agreed well with Fukui index prediction. The toxicity of DCF was alleviated during the degradation process through successful mineralization of chlorine atoms.
引用
收藏
页数:13
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