Tuning the structure of Co3O4@MnOx catalyst by in situ redox approach for enhancing activity of the catalytic combustion of toluene

被引:8
作者
Liu, Wei [1 ]
Cui, Ruoyang [1 ]
Chen, Xi [2 ]
Zhang, Shuning [2 ]
Xiang, Wenjie [2 ]
Zhang, Xuejun [2 ]
机构
[1] Shenyang Univ Chem Technol, Coll Sci, Shenyang 110142, Peoples R China
[2] Shenyang Univ Chem Technol, Coll Environm & Safety Engn, Shenyang 110142, Peoples R China
基金
中国国家自然科学基金;
关键词
VOCs; Catalytic combustion of toluene; Co3O4 based catalysts; In-situ oxidation strategy; OXIDATION; CO; OXIDES; CO3O4; SURFACE; COOXIDATION; FABRICATION; VOCS; MNOX;
D O I
10.1016/j.jssc.2022.123347
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A novel in-situ redox method is proposed to prepare Co3O4 based catalysts with a core-shell-like structure toward the catalytic oxidation of toluene. The results of XRD, SEM and HRTEM reveal that Co3O4@MnOx with a coreshell-like structure was obtained after the precursor was partially oxidized by potassium permanganate. The as-prepared Co3O4@MnOx catalyst exhibits considerably high efficiency for the catalytic combustion of toluene, achieving 90% conversion of toluene at 233 degrees C that is at least 65 degrees C lower than that of the sole Co3O4 sample. The real reason is that Co3O4@MnOx is remarkably active than the other samples was explored by analyzing the results of a series of characterizations including Raman, XPS, TEM and H-2-TPR. The results show that the catalytic activity of the samples is affected by the amount of Co3+ species, the concentration of oxygen species, and the content of oxygen vacancies to some extent, however, the result of H-2-TPR indicates that their reactivity rather than the absolute content is the decisive factor for the activity of these catalysts. In addition, Co3O4@MnOx presents a satisfactory long-term stability, suggesting its great potential in industrial application.
引用
收藏
页数:9
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