4.7 Article

Theoretical investigation of solvent effects on the selective hydrogenation of furfural over Pt(111)

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 46, Issue 2, Pages 1592-1604

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2020.10.066

Keywords

Furfural; Selective hydrogenation; Pt(111); Solvent effect; DFT; Microkinetic analysis

Funding

  1. National Natural Science Foundation of China [21773123, 2142100, 91545106]
  2. Shanxi Province Natural Science Foundation [201801D121037]
  3. Intramural Foundation of Taiyuan University of Science and Technology [202023, 202024]

Ask authors/readers for more resources

This study demonstrates the importance of solvent effect in catalytic reactions, with methanol being able to enhance adsorption strength of reaction species and improve activity and selectivity in the hydrogenation of furfural over Pt(111). The presence of methanol contributes to a less thermochemical dehydrogenation of furfural and inhibits the dehydrogenation reaction, leading to higher activity and selectivity. Microkinetic model simulations showed that hydrogenation in methanol exhibited higher activity and selectivity compared to other solvents like vapor and toluene, indicating that a solvent with relatively strong polarity may favor the selective hydrogenation of furfural.
It was well known that solvent effect plays a very important role in the catalytic reaction. There are many theoretical studies on the solvent effect in homogeneous catalysis while there are few theoretical studies on the solvent effect in the heterogeneous catalytic reaction and there has been no work to investigate the solvent effect on furfural transformation in heterogeneous catalysis. In the present work, both the density functional calculations and the microkinetic analysis were performed to study the selective hydrogenation of furfural over Pt(111) in the presence of methanol as well as toluene and compared with that in the gas condition. The present results indicated that the methanol can enhance the adsorption strength of furfural and other oxygen-containing reaction species due to its relatively strong polarity properties and this can be a main reason for solvent-induced high activity and selectivity. Another reason is that reaction paths study showed that the presence of methanol solvent makes the dehydrogenation of furfural less thermochemical due to the fact that furfural is more stabilized than that of dehydrogenation species, and methanol also has an inhibition effect on the dehydrogenation of furfural in the kinetic aspect, and further energetic span theory proves highest activity and selectivity for hydrogenation in methanol solvent of vapor, methanol and toluene. Moreover, microkinetic model simulation demonstrated that the activity and selectivity of hydrogenation in methanol is both higher than that in vapor and toluene. The much higher activity in methanol is due to the stabilized adsorbed reactants in the surface, which leads to a higher surface coverage of furfural. It might be proposed based on the present work that a solvent with relatively strong polarity may be favorable for the high selective hydrogenation of furfural. (C) 2020 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.7
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available