Effect of thermal pretreatment on the surface structure of PtSn/SiO2 catalyst and its performance in acetic acid hydrogenation

Guozhen Xu, Jian Zhang, Shengping Wang, Yujun Zhao, Xinbin Ma

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PDF(383 KB)
Front. Chem. Sci. Eng. ›› 2016, Vol. 10 ›› Issue (3) : 417-424. DOI: 10.1007/s11705-016-1583-1
RESEARCH ARTICLE
RESEARCH ARTICLE

Effect of thermal pretreatment on the surface structure of PtSn/SiO2 catalyst and its performance in acetic acid hydrogenation

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Abstract

The effect of thermal pretreatment on the active sites and catalytic performances of PtSn/SiO2 catalyst in acetic acid (AcOH) hydrogenation was investigated in this article. The catalysts were characterized by N2 physical adsorption, X-ray diffraction, transmission electron microscopy, pyridine Fourier-transform infrared spectra, and H2-O2 titration on its physicochemical properties. The results showed that Pt species were formed primarily in crystalline structure and no PtSnx alloy was observed. Meanwhile, with the increment of thermal pretreatment temperature, Pt dispersion showed a decreasing trend due to the aggregation of Pt particles. Simultaneously, the amount of Lewis acid sites was remarkably influenced by such thermal pretreatment owning to the consequent physicochemical property variation of Sn species. Interestingly, the catalytic activity showed the similar variation trend with that of Lewis acid sites, confirming the important roles of Lewis acid sites in AcOH hydrogenation. Moreover, a balancing effect between exposed Pt and Lewis acid sites was obtained, resulting in the superior catalytic performance in AcOH hydrogenation.

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Keywords

thermal pretreatment / acetic acid / hydrogenation / ethanol / PtSn/SiO2

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Guozhen Xu, Jian Zhang, Shengping Wang, Yujun Zhao, Xinbin Ma. Effect of thermal pretreatment on the surface structure of PtSn/SiO2 catalyst and its performance in acetic acid hydrogenation. Front. Chem. Sci. Eng., 2016, 10(3): 417‒424 https://doi.org/10.1007/s11705-016-1583-1

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Acknowledgments

We are grateful to the financial support from the National Natural Science Foundation of China (Grant Nos. 21276186, 21325626, 91434127, U1510203) and the Tianjin Natural Science Foundation (13JCZDJC33000).

Electronic Supplementary Material

Supplementary material is available in the online version of this article at http://dx.doi.org/10.1007/s11705-016-1583-1 and is accessible for authorized users.
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2016 Higher Education Press and Springer-Verlag Berlin Heidelberg
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