1. Shifting reaction path for levulinic acid aqueous-phase hydrogenation by Pt-TiO2 metal-support interaction.
- Author
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Meng, Fanchun, Yang, Xinchun, Zhao, Shichao, Li, Zhuo, Zhang, Guikai, Qi, Yuntao, Chu, Shengqi, Wang, Guofu, Zhang, Jing, Qin, Yong, and Zhang, Bin
- Subjects
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HYDROGENATION , *ATOMIC layer deposition , *FOURIER transform infrared spectroscopy , *WATER gas shift reactions , *POROSITY - Abstract
Levulinic acid (LA) aqueous-phase hydrogenation into γ-valerolactone (GVL) is considered one of the pivotal reactions to convert biomass into renewable chemicals. Here we have deposited Pt on TiO 2 nanofilm coated α-Al 2 O 3 via atomic layer deposition (ALD) to synthesize Pt-TiO 2 /α-Al 2 O 3. This catalyst shows excellent activity and stability (1000 h) in LA hydrogenation compared to Pt/α-Al 2 O 3. By excluding the effect of Pt particle size, lattice plane, support morphology, pore structure, and electronic state, the critical role of Pt-TiO 2 interaction is revealed by various characterization methods. CO diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) and in-situ Fourier transform Infrared spectra (FTIR) results indicate that Pt-TiO 2 interaction provides new interfacial Pt sites for LA and intermediate adsorption and Ti-OH active sites for LA dehydration cyclization to α-angelica lactone intermediate, which leads to the shift of reaction pathways from direct LA C O hydrogenation lactonization on Pt/α-Al 2 O 3 to LA dehydration cyclization and hydrogenation on Pt-TiO 2 /α-Al 2 O 3。 It provides insight into the design of high-efficient catalysts for aqueous-phase hydrogenation. [Display omitted] • The critical role of Pt-TiO 2 interaction is revealed by excluding the effect of Pt structures. • Pt-TiO 2 interaction provides interfacial Pt sites and Ti-OH sites for LA dehydration cyclization. • Pt-TiO 2 interaction cause the shift of reaction pathways for LA hydrogenation. [ABSTRACT FROM AUTHOR]
- Published
- 2023
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