Boosting toluene deep oxidation by tuning metal-support interaction in MOF-derived Pd@ZrO2 catalysts: The role of interfacial interaction between Pd and ZrO2

被引:98
作者
Bi, Fukun [1 ,2 ]
Ma, Shuting [1 ]
Gao, Bin [1 ]
Liu, Baolin [2 ]
Huang, Yuandong [1 ]
Qiao, Rong [1 ]
Zhang, Xiaodong [1 ,3 ]
机构
[1] Univ Shanghai Sci & Technol, Sch Environm & Architecture, Shanghai 200093, Peoples R China
[2] Univ Shanghai Sci & Technol, Sch Hlth Sci & Engn, Shanghai 200093, Peoples R China
[3] Shanghai Noncarbon Energy Convers & Utilizat Inst, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
Toluene deep oxidation; Metal -support interaction; MOF derivatives; Supported Pd catalysts; Interfacial interaction; OXYGEN VACANCIES; ACTIVE-SITES; PERFORMANCE; COBALT; COMBUSTION; PD/ZRO2; OXIDE;
D O I
10.1016/j.fuel.2023.129833
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The regulation of metal-support interaction is one of the productive strategies to enhance volatile organic compounds (VOCs) deep degradation. Herein, Pd@ZrO2 catalysts were synthesized via using in-situ growth Zr-based metal organic framework (MOF) Pd@UiO-66 as the precursor to boost toluene deep degradation. Compared with Pd@ZrO2-Zr(OH)4 synthesized by using Zr(OH)4 as the precursor, MOF-derived Pd@ZrO2 catalysts with different calcination time exhibited more superior catalytic performance, water-resistance and stability. Characterizations results indicated the occurrence of interfacial interaction in MOF-derived Pd@ZrO2 induced the better reducibility at low-temperature and the generation of oxygen vacancies, enhanced Oads species content, weakened Zr-O bond strength, improved the mobility of Olat species, which caused its better toluene degradation performance. Simultaneously, in-situ diffuse reflectance infrared Fourier transform spec-troscopy results clarified that the interfacial interaction heightened the adsorption and activation ability for gaseous oxygen to form reactive oxygen species and replenish consumed Olat species, promoted toluene ring -opening reaction, reduced benzoate acid species cumulation, expedited the fast deeply degradation of toluene to CO2 and H2O. This work may provide a new perspective on MOF-derived catalysts with better performance for VOCs degradation deeply by tuning interfacial interaction.
引用
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页数:13
相关论文
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