One-pot hard template synthesis of mesoporous spinel nanoparticles as efficient catalysts for low temperature CO oxidation

被引:2
|
作者
Mobini, Sajad [1 ]
Rezaei, Mehran [2 ]
Meshkani, Fereshteh [1 ]
机构
[1] Univ Kashan, Fac Engn, Chem Engn Dept, Catalyst & Adv Mat Res Lab, Kashan, Iran
[2] Iran Univ Sci & Technol IUST, Sch Chem Petr & Gas Engn, Tehran, Iran
基金
美国国家科学基金会;
关键词
CO oxidation; Mixed oxide; Catalyst; Hard template; Spinel; PALLADIUM FIELD EMITTER; COPPER-MANGANESE OXIDE; CARBON-MONOXIDE; SURFACE-AREA; PERFORMANCE; METHANE; KINETICS; MN; LA0.6SR0.4MNO3; COMBUSTION;
D O I
10.1007/s11356-020-10398-8
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Co-Fe, Cu-Cr, and Co-Mn mixed oxide catalysts were prepared using a one-pot hard template synthesis method, and their catalytic performance was investigated before and after the rearrangement of the template. To evaluate the structural properties of the catalysts, various analyses were employed, including the BET, XRD, H-2-TPR, FE-SEM, EDX, and X-ray digital mapping of the elements. The results indicated that the rearrangement of the catalyst structure had a profound effect on the structural and catalytic properties, so that in all three synthesized catalysts, the specific surface and the reducibility increased significantly, and the crystalline structure and morphology of the catalysts changed remarkably. The specific surface area of the CoFe, CuCr, and CoMn catalysts increased from 3.5, 1.1, and 72.9 m(2)/g to 151.3, 52.8, and 108.0 m(2)/g, respectively. These structural changes significantly increased the catalytic performance. The results indicated that the 100% conversion temperature of the CoMn catalyst as the optimal sample after rearrangement was reduced from 250 to 125 degrees C. Also, the stability of the CoMn catalyst in dry and wet conditions was investigated and the results indicated that the presence of water vapor reduced the activity and stability of the catalyst. The activation energy was also calculated on Co-Mn catalyst (59.5 kJ/mol) and the results confirmed that the most probable mechanism for this reaction was the MVK mechanism.
引用
收藏
页码:547 / 563
页数:17
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