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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.
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页数:14
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