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Effect of surface properties of TiO2 on the performance of Pt/TiO2 catalysts for furfural hydrogenation
被引:29
作者:
Byun, Mi Yeon
[1
,2
]
Kim, Ye Eun
[1
,4
]
Baek, Jae Ho
[1
]
Jae, Jungho
[3
]
Lee, Man Sig
[1
,5
]
机构:
[1] Korea Inst Ind Technol KITECH, Ulsan Div, Ulsan 44413, South Korea
[2] Pusan Natl Univ, Dept Polymer Sci & Chem Engn, Busan 46241, South Korea
[3] Pusan Natl Univ, Sch Chem Engn, Busan 46241, South Korea
[4] Korea Univ, Dept Chem & Biol Engn, Seoul 02841, South Korea
[5] Univ Sci & Technol UST, Dept Green Proc & Syst Engn, Ulsan 44413, South Korea
关键词:
HIGHLY SELECTIVE REARRANGEMENT;
COBALT CATALYSTS;
CO OXIDATION;
CONVERSION;
PD;
ALCOHOL;
PHASE;
METAL;
NANOWIRES;
CYCLOPENTANOL;
D O I:
10.1039/d1ra07220j
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
Hydrogenation of biomass-derived furfural is an important process in biofuel production. Herein, different Pt-supported TiO2 morphologies: nanorod (NR), nanoparticle (NP), and hollow microsphere (HMS) were prepared by the impregnation-chemical reduction method. The furfural conversion increased with an increase of Pt dispersion. However, cyclopentanone selectivity was affected by TiO2 properties, the strong metal-support interaction (SMSI) effect, and the reaction conditions. The Pt/TiO2 NR catalyst exhibited the highest cyclopentanone selectivity of 50.4%. Based on the H-2-temperature programmed desorption (H-2-TPD) and X-ray photoelectron spectroscopy (XPS) results, the Pt/TiO2 NR catalyst showed a SMSI effect, which was introduced by the chemical reduction method. We suggest that electron charge transfer from Ti species to Pt in the Pt/TiO2 NR catalyst affects the cyclopentanone selectivity by controlling the adsorption strength between the reactant and the Pt surface, thus retarding the formation of byproducts.
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页码:860 / 868
页数:9
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