中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
In-situ synthesis of N, S co-doped hollow carbon microspheres for efficient catalytic oxidation of organic contaminants

文献类型:期刊论文

作者Xie, Yongbing1,2; Liu, Ya3,4; Yao, Yujie2,5; Shi, Yanchun2; Zhao, Binran5; Wang, Yuxian3
刊名CHINESE CHEMICAL LETTERS
出版日期2022-03-01
卷号33期号:3页码:1298-1302
ISSN号1001-8417
关键词Metal-free catalysis Hollow carbon microspheres N, S co-doping Catalytic ozonation Singlet oxygen (O-1(2))
DOI10.1016/j.cclet.2021.07.055
英文摘要Metal-free heteroatom doped nanocarbons are promising alternatives to the metal-based materials in catalytic ozonation for destruction of aqueous organic contaminants. In this study, N, S co-doped hollow carbon microspheres (NSCs) were synthesized from the polymerization products during persulfate wet air oxidation of benzothiazole. The contents of doped N and S as well as the structural stability were maneuvered by adjusting the subsequent N-2-annealing temperature. Compared with the prevailing single-walled carbon nanotubes, the N-2-annealed NSCs demonstrated a higher catalytic ozonation activity for benzimidazole degradation. According to the quantitative structure-activity relationship (QSAR) analysis, the synergistic effect between the graphitic N and the thiophene-S which redistributed the charge distribution of the carbon basal plane contributed to the activity enhancement of the N-2-annealed NSCs. Additionally, the hollow structure within the microspheres served as the microreactor to boost the mass transfer and reaction kinetics via the nanoconfinement effects. Quenching and electron paramagnetic resonance (EPR) tests revealed that benzimidazole degradation was dominated by the produced singlet oxygen (O-1(2)) species, while hydroxyl radicals ((OH)-O-center dot) were also generated and participated. This study puts forward a novel strategy for synthesis of heteroatom-doped nanocarbons and sheds a light on the relationship between the active sites on the doped nanocarbons and the catalytic performance. (C) 2021 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
WOS关键词SINGLET OXYGEN ; PEROXYMONOSULFATE ACTIVATION ; WATER-TREATMENT ; RATE CONSTANTS ; DEGRADATION ; OZONATION ; GRAPHENE ; PERSULFATE ; NANOTUBES ; OXIDE
资助项目National Natural Science Foundation of China[21978324] ; Tianjin Municipal Science and Technology Bureau[18YFYSZ00170] ; Beijing Natural Science Foundation[8192039] ; Science Foundation of China University of Petroleum, Beijing[2462020YXZZ034]
WOS研究方向Chemistry
语种英语
出版者ELSEVIER SCIENCE INC
WOS记录号WOS:000772416400023
资助机构National Natural Science Foundation of China ; Tianjin Municipal Science and Technology Bureau ; Beijing Natural Science Foundation ; Science Foundation of China University of Petroleum, Beijing
源URL[http://ir.ipe.ac.cn/handle/122111/52524]  
专题中国科学院过程工程研究所
通讯作者Zhao, Binran; Wang, Yuxian
作者单位1.State Key Lab Vanadium & Titanium Resources Compr, Panzhihua 617000, Peoples R China
2.Chinese Acad Sci, Inst Proc Engn, CAS Key Lab Green Proc & Engn, Beijing Engn Res Ctr Proc Pollut Control, Beijing 100190, Peoples R China
3.China Univ Petr, State Key Lab Petr Pollut Control, State Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China
4.Univ Adelaide, Sch Chem Engn & Adv Mat, Adelaide, SA 5005, Australia
5.Northwest Univ, Sch Chem Engn, Xian 710069, Peoples R China
推荐引用方式
GB/T 7714
Xie, Yongbing,Liu, Ya,Yao, Yujie,et al. In-situ synthesis of N, S co-doped hollow carbon microspheres for efficient catalytic oxidation of organic contaminants[J]. CHINESE CHEMICAL LETTERS,2022,33(3):1298-1302.
APA Xie, Yongbing,Liu, Ya,Yao, Yujie,Shi, Yanchun,Zhao, Binran,&Wang, Yuxian.(2022).In-situ synthesis of N, S co-doped hollow carbon microspheres for efficient catalytic oxidation of organic contaminants.CHINESE CHEMICAL LETTERS,33(3),1298-1302.
MLA Xie, Yongbing,et al."In-situ synthesis of N, S co-doped hollow carbon microspheres for efficient catalytic oxidation of organic contaminants".CHINESE CHEMICAL LETTERS 33.3(2022):1298-1302.

入库方式: OAI收割

来源:过程工程研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。