Acidity modulation of Pt-supported catalyst enhances C-O bond cleavage over acetone hydrodeoxygenation

被引:11
|
作者
Strapasson, Guilherme B. [1 ,2 ]
Sousa, Leonardo S. [1 ]
Bafero, Gabriel B. [1 ]
Leite, Davi S. [1 ]
Moreno, Beatriz D. [3 ]
Rodella, Cristiane B. [2 ]
Zanchet, Daniela [1 ]
机构
[1] Univ Estadual Campinas, Inst Chem, UNICAMP, BR-13083970 Campinas, SP, Brazil
[2] Brazilian Synchrotron Light Lab, CNPEM, BR-13083100 Campinas, SP, Brazil
[3] Canadian Light Source Inc, 44 Innovat Blvd, Saskatoon, SK S7N 2V3, Canada
来源
APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY | 2023年 / 335卷
关键词
Catalysis; Hydrodeoxygenation; Metal-support interaction; Mixed metal oxides; Acidity; STABLE SINGLE-ATOM; TITANATE NANOTUBES; BASE PAIRS; METAL TYPE; LEWIS; PHENOL; WATER; PD; DEHYDRATION; REACTIVITY;
D O I
10.1016/j.apcatb.2023.122863
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Understanding how to tune the properties of metal oxides, e.g., controlling and manipulating defects and cat-alytic sites, and establishing a clear understanding of metal support interactions is essential for developing catalysts with enhanced activity, selectivity, and stability. Here, we report the synthesis of Pt-supported Ti-Nb mixed metal oxides, aiming for the acidity modulation of Bronsted and Lewis acid sites of the catalysts' surface. Results demonstrated that the catalyst richer in Bronsted acid sites was a promising candidate for the acetone hydrodeoxygenation reaction, with enhanced stability and preferential selectivity toward C-O bond cleavage during the time on stream. Important insights into the impact of acidity modulation of Pt-supported catalysts were presented here, especially concerning the metal-support interaction. The intrinsic correlation between catalytic sites and reaction mechanism was also discussed.
引用
收藏
页数:14
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