4.6 Article

Insights into Hydrodeoxygenation of Furfural and Guaiacol Mixture: Experimental and Theoretical Studies

期刊

JOURNAL OF PHYSICAL CHEMISTRY C
卷 125, 期 14, 页码 7647-7657

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.0c11415

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资金

  1. ANID Chile [1180982, AFB170007, EQM160070]
  2. Millennium Science Initiative Program [NCN17_040]
  3. CSIC [20211]

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The catalytic hydrodeoxygenations of furfural and guaiacol, as well as their mixture, were studied over a Ni/SiO2 catalyst. Guaiacol was found to increase the reaction rate of furfural and slightly change the selectivity of products, attributed to the migration of the hydroxyl group to furfural. These effects would be enhanced by increasing the guaiacol concentration, which could act as a stabilizing agent inhibiting coke formation.
Catalytic hydrodeoxygenations of furfural, guaiacol, and their mixture at different concentrations were carried out over a Ni/SiO2 catalyst to study the kinetic and competitive effects. Anisole was also studied to compare with the effects of guaiacol. Additionally, kinetic parameters were adjusted through mathematical modeling to explain the mixture behavior, and density functional theory (DFT) simulations were carried out to study the effect observed in the present work. The use of guaiacol and anisole in the mixture produces an increase in the reaction rate of furfural. Furthermore, guaiacol slightly generates a change in the selectivity of furfural products, attributed to its hydroxyl group, as such a change was not observed with anisole. DFT studies showed that the hydrogen atom of the hydroxyl group of guaiacol migrated to furfural. Both effects would be enhanced by increasing the guaiacol concentration, which could act as a stabilizing agent inhibiting the coke formation in the furfural reaction.

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