Cation deficiency tuned LaCoO3-δ perovskite for peroxymonosulfate activation towards bisphenol A degradation

被引:102
作者
Liang, Ping [1 ]
Meng, Dingding [1 ]
Liang, Yi [1 ]
Wang, Zheng [1 ]
Zhang, Chi [1 ]
Wang, Shaobin [2 ]
Zhang, Zhonghua [1 ,3 ]
机构
[1] Wuyi Univ, Sch Appl Phys & Mat, Jiangmen, Peoples R China
[2] Univ Adelaide, Sch Chem Engn & Adv Mat, Adelaide, SA 5005, Australia
[3] Shandong Univ, Sch Mat Sci & Engn, Key Lab Liquid Solid Struct Evolut & Proc Mat, Minist Educ, Jinan, Peoples R China
基金
中国国家自然科学基金;
关键词
Advanced oxidation process; Deficiency tunning; Singlet oxygen; Sulfate radical; Oxygen vacancies; ORGANIC POLLUTANTS; HETEROGENEOUS ACTIVATION; CATALYTIC-OXIDATION; EFFICIENT REMOVAL; HYDROXYL RADICALS; CARBON NANOTUBES; MANGANESE OXIDES; SULFATE; OXYGEN; MN;
D O I
10.1016/j.cej.2020.128196
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Perovskite-based materials have been demonstrated to be effective for peroxymonosulfate (PMS) activation towards wastewater treatment. However, the effect of cation deficiency in perovskite oxides has not been well illustrated. In this study, cation deficient LaCoO3-delta perovskite oxides have been prepared to tune the catalytic activity. B-site cation deficiency on the LaCoO3-delta perovskite oxides promotes the catalytic performance while Asite cation deficiency is detrimental to the catalysis for PMS activation. The first-order kinetic rate of B-site cation deficient LaCoO3-delta pemvskites prepared via sol-gel method is 0.591 min(-1), higher than that of LaCoO3-delta perovskites with A-site cation deficiency (0.118 min(-1)) and no cation deficiency (0.243 min(-1)). About 90% of organics could be mineralized completely through the catalysis of B-site cation deficient LaCoO3-delta perovskites in 60 min. The sulfate radicals and singlet oxygen are responsible for the catalytic degradation of bisphenol A. The surface Co(II) site, surface hydroxyl group and oxygen vacancies on the LaCoO3-delta pemvskite oxides are the active sites for catalysis. The excellent catalytic activity induced by B-site cation deficiency can be attributed to the high charge transfer and surface reaction rate, abundant Co(II) site, surface hydroxyl group and oxygen vacancies.
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页数:10
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