Porous hollow CoInOx nanocubes as a highly efficient catalyst for the catalytic combustion of toluene

被引:30
作者
Dong, Fang [1 ,2 ]
Han, Weiliang [1 ,2 ]
Zhao, Haijun [1 ,2 ]
Zhang, Guodong [1 ,2 ]
Tang, Zhicheng [1 ,2 ]
机构
[1] Chinese Acad Sci, Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Gansu, Peoples R China
[2] Chinese Acad Sci, Lanzhou Inst Chem Phys, Natl Engn Res Ctr Fine Petrochem Intermediates, Lanzhou 730000, Gansu, Peoples R China
基金
中国国家自然科学基金; 中国科学院西部之光基金;
关键词
CARBON-MONOXIDE; TOTAL OXIDATION; SUPPORTED GOLD; COBALT OXIDE; PERFORMANCE; CO; NANOPARTICLES; NANOCATALYSTS; REDUCTION; BENZENE;
D O I
10.1039/c8nr10052g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Porous hollow HC-CoInOx nanocubes were synthesized via a SiO2 template strategy involving a cobalt-based metal-organic framework derived from a Prussian Blue analogue. As a heterogeneous catalytic material for the catalytic combustion of toluene, the hollow HC-CoInOx nanocubes displayed superior catalytic performance (T-90 = 178 degrees C) and greatly reduced the activation energy for toluene oxidation due to their large surface area, the formation of surface dangling bands and oxygen vacancies, and increased number of weak acid sites. In comparison, the C-CoInOx sample (without the introduction of a SiO2 template) required a higher reaction temperature to achieve the same conversion of toluene (T-90 = 345 degrees C). Especially, the insertion and coating of SiO2 in CoIn-PBA nanocubes greatly improves their thermal stability, and the nanocubic shape of the porous hollow HC-CoInOx sample can remain intact after roasting at 450 degrees C, while the nanocubic shape of the C-CoInOx sample without the introduction of SiO2 is partially damaged and suffers from serious aggregation under the same firing conditions. Simultaneously, the porous hollow HC-CoInOx nanocubes also exhibited excellent cycling and thermal stability for the catalytic combustion of toluene to CO2 and H2O.
引用
收藏
页码:9937 / 9948
页数:12
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