Abstract

The impact of using different nanostructured carbon materials (carbon nanofibers, carbon nanotubes, graphene oxide and activated carbon) as a support for Mo2C-based catalysts on the hydrodeoxygenation (HDO) of guaiacol was studied. To optimise the catalyst preparation by carbothermal hydrogen reduction (CHR), a thermogravimetric study was conducted to select the optimum CHR temperature for each carbon material, considering both the crystal size of the resulting β-Mo2C particles and the extent of the support gasification. Subsequently, catalysts were prepared in a fixed bed reactor at the optimum temperature. Catalyst characterization evidenced the differences in the catalyst morphology as compared to those prepared in the thermogravimetric study. The HDO results demonstrated that the carbon nanofiber-based catalyst was the one with the best catalytic performance. This behaviour was attributed to the high thermal stability of this support, which prevented its gasification and promoted a good evolution of the crystal size of Mo species. This catalyst exhibited well-dispersed β-Mo2C nanoparticles of ca. 11 nm. On the contrary, the other supports suffered from severe gasification (60–70% wt. loss), which resulted in poorer HDO efficiency catalysts regardless of the β-Mo2C crystal size. This exhibited the importance of the carbon support stability in Mo2C-based catalysts prepared by CHR.

Highlights

  • Since the development in 1985 by Boudart et al of high specific surface area carbides and nitrides by temperature-programmed reduction [1], several authors have synthetised Mo2 C catalysts by this method using hydrocarbon/hydrogen mixtures [2,3,4,5,6,7,8]

  • The other supports suffered from severe gasification (60–70% wt. loss), which resulted in poorer HDO efficiency catalysts regardless of the β-Mo2 C crystal size

  • The nanostructured carbon materials had a direct effect on the formation of β-Mo2 C in the carbothermal hydrogen reduction and in the hydrodeoxygenation of guaiacol

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Summary

Introduction

Since the development in 1985 by Boudart et al of high specific surface area carbides and nitrides by temperature-programmed reduction [1], several authors have synthetised Mo2 C catalysts by this method using hydrocarbon/hydrogen mixtures [2,3,4,5,6,7,8]. Mo2 C catalysts, the carbothermal hydrogen reduction (CHR) method may transform Mo oxides into hexagonal-close-packed carbides (β-Mo2 C) at relatively moderate temperatures (

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