期刊
RSC ADVANCES
卷 12, 期 2, 页码 860-868出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d1ra07220j
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资金
- Korea Institute of Industrial Technology through Research and Development [EH210006, EO210001]
- Ulsan Metropolitan City [IZ210064]
- National Research Council of Science & Technology (NST), Republic of Korea [EH210006, EO210001] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
The study investigated the effect of different morphologies of Pt/TiO2 catalysts on the hydrogenation of biomass-derived furfural, finding that the Pt/TiO2 NR catalyst exhibited high cyclopentanone selectivity mainly due to the electron charge transfer from Ti species to Pt causing a strong metal-support interaction effect.
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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