Polyaniline@g-C3N4 derived N-rich porous carbon for selective degradation of phenolic pollutants via peroxymonosulfate activation: An electron transfer mechanism

被引:15
作者
Kou, Lidong [1 ,2 ]
Fan, Qingfeng [1 ]
Yang, Yuhong [3 ]
Duan, Xianying [2 ]
Jiang, Kai [1 ]
Wang, Jing [2 ,4 ]
机构
[1] Henan Normal Univ, Sch Environm, Key Lab Yellow River & Huai River Water Environm &, Henan Key Lab Environm Pollut Control, Xinxiang 453007, Henan, Peoples R China
[2] Henan Acad Sci, Inst Chem, Zhengzhou 450002, Henan, Peoples R China
[3] North China Univ Water Resources & Elect Power, Sch Water Conservancy, Zhengzhou 450046, Henan, Peoples R China
[4] 56 Hongzhuan Rd, Zhengzhou 450002, Peoples R China
基金
中国国家自然科学基金;
关键词
N -doped porous carbon; Polyaniline; Electron transfer pathway; Peroxymonosulfate; DOPED GRAPHENE; ORGANIC POLLUTANTS; OXIDATION; TRANSFORMATION; NANOSHEETS; CATALYST; NITRIDE; G-C3N4; WATER;
D O I
10.1016/j.chemosphere.2022.137022
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
N-doped carbons have attracted extensive attention as catalysts for peroxymonosulfate (PMS) activation towards environmental remediation. However, synthesis of N-rich carbocatalysts is challenging and PMS activation mechanism is still unclear. Herein, novel N-rich porous carbocatalysts (C-PxCN-T) were synthesized by carbonization of polyaniline nanorods coated g-C3N4. C-P50CN-900 (polyaniline content 50%) calcined at 900 degrees C had high surface area (358 m2/g), product yield (27.1%) and N content (12.27 at%). It showed superior performance in activating PMS to degrade and mineralize various phenolic pollutants in a wide pH range (2-11) and with the co-existence of water constituents. A positive correlation was observed between phenol oxidation rates and contents of C--O, C-C/C--C and graphitic N, which served as active sites to facilitate adsorption of pollutants and PMS on C-P50CN-900 and subsequent electron-transfer from pollutants to PMS. Overall, this study provides new insights into rational design of N-doped carbocatalysts and elucidation of electron transfer pathway in PMS activation.
引用
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页数:11
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