Cobalt nanoparticles supported on porous carbon nanofiber as efficient catalyst for heterogeneous activation of peroxymonosulfate towards the degradation of organic pollutants

被引:6
|
作者
Yang, Qin [1 ]
Yang, Yingchun [1 ]
Zhang, Yujie [1 ]
Ren, Yuchun [2 ]
Chen, Qiru [2 ]
Fang, Xiaodong [3 ]
Sun, Shengjun [2 ]
Zhang, Longcheng [2 ]
Zhang, Xuefeng [1 ]
Luo, Yongsong [2 ]
Liu, Qian [3 ]
Sun, Xuping [2 ,4 ]
机构
[1] Chengdu Univ Informat Technol, Coll Resources & Environm, Chengdu 610225, Sichuan, Peoples R China
[2] Univ Elect Sci & Technol China, Inst Fundamental & Frontier Sci, Chengdu 610054, Sichuan, Peoples R China
[3] Chengdu Univ, Inst Adv Study, Chengdu 610106, Sichuan, Peoples R China
[4] Shandong Normal Univ, Coll Chem, Chem Engn & Mat Sci, Jinan 250014, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Cobalt nanoparticles; Porous carbon nanofiber; Heterogeneous activation; Peroxymonosulfate; Carbamazepine; PERSULFATE ACTIVATION; OXIDATION; GENERATION; GRAPHENE; MECHANISMS; KINETICS; CO3O4; WATER; OXIDE;
D O I
10.1016/j.psep.2023.06.080
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
In this work, cobalt-porous carbon nanofiber (Co-PCNF) was developed as a robust catalyst for the activation of peroxymonosulfate (PMS) to eliminate organic pollutants in water. Carbamazepine (CBZ) was severed as the probe to examine the ability of Co-PCNF for activating PMS. The microporous honeycomb-like structure endowed Co-PCNF with excellent catalytic activity to activate PMS as evidenced by the rapid removal rate of CBZ (0.1269 min(-1)) in the existence of 0.1 g/L Co-PCNF and 0.25 g/L PMS. The degradation rate of CBZ can be maintained at 89 % after five runs and the leaching concentration of Co2+ can be neglected, suggesting the extraordinary stability of Co-PCNF reuse. Meanwhile, this system was used to degrade other organic contaminates and achieved satisfactory results, confirming the good universality of Co-PCNF/PMS system. Furthermore, the effects of catalyst and PMS dosage, pH, and co-existing ions on CBZ removal were discussed. Finally, radical identification results prove that SO4 center dot-,center dot OH, O-1(2), and O-2(center dot-) are generated during the process of PMS activation, and a possible activation mechanism is proposed based on the aforementioned findings. This study can not only provide a method for organic pollutants elimination, but also offer a reference for designing robust heterogeneous PMS catalysts.
引用
收藏
页码:988 / 996
页数:9
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