Perovskite CaZrO3 for efficient ozonation treatment of organic pollutants in wastewater

被引:24
作者
Han, Peiwei [1 ,2 ]
Lv, Hongxia [1 ]
Li, Xiaogang [1 ]
Wang, Shengzhe [2 ]
Wu, Zhilian [3 ,4 ]
Li, Xiangnan [5 ]
Mu, Zhao [1 ]
Li, Xinjun [5 ]
Sun, Chenglin [2 ]
Wei, Huangzhao [2 ]
Ma, Lei [1 ]
机构
[1] Beijing Inst Petrochem Technol, Beljing Key Lab Fuels Cleaning & Adv Catalyt Emis, Coll Chem Engn, Beijing 102617, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
[3] Ningbo Fengcheng Adv Energy Mat Res Inst Co Ltd, Ningbo 315500, Zhejiang, Peoples R China
[4] Shenzhen Univ, Coll Mat Sci & Engn, Shenzhen 518055, Guangdong, Peoples R China
[5] Chinese Acad Sci, Guangzhou Inst Energy Convers, Guangzhou 510640, Peoples R China
关键词
CATALYTIC OZONATION; OXYGEN VACANCIES; OXIDE CATALYSTS; ACTIVE-SITE; OXIDATION; ACID; DEGRADATION; PERFORMANCE; ACTIVATION; DECOMPOSITION;
D O I
10.1039/d0cy02404j
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
Catalytic ozonation with nano-perovskite oxides is a more efficient and advanced oxidation process for the mineralization of organic pollutants. In this study, by regulating the amount of polyethylene glycol during the synthesis of CaZrO3 perovskite-type oxides by the co-precipitation method, efficient surface oxygen vacancies were formed in CaZrO3. Owing to the presence of abundant oxygen vacancies, CaZrO3 modified by PEG exhibited a much higher catalytic activity than unmodified CaZrO3. It was further discovered from the EPR results that the main active oxygen species depend on the surface structure of CaZrO3. The variation of oxygen vacancies on the surface of the catalyst with PEG addition stimulated ozone decomposition to generate a large number of superoxide radicals. This study not only proposed a method to improve the activity of the catalyst, but also further studied the reaction mechanism of CaZrO3 catalyzed ozonation. It provides a solid theoretical basis for the industrial application of catalytic ozonation technology.
引用
收藏
页码:3697 / 3705
页数:9
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