Vanillin Hydrodeoxygenation: Kinetic Modelling and Solvent Effect
Vanillin hydrodeoxygenation was investigated using Pt/C catalyst in the temperature and total pressure ranges of 80–200 °C and 20–30 bar in several solvents, such as tetrahydrofuran, 2-propanol, water and in solventless conditions using 1:1 mass ratio of vanillin to guaiacol. The results revealed th...
Saved in:
Published in | Catalysis letters Vol. 148; no. 9; pp. 2856 - 2868 |
---|---|
Main Authors | , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Springer US
01.09.2018
Springer Springer Nature B.V |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Vanillin hydrodeoxygenation was investigated using Pt/C catalyst in the temperature and total pressure ranges of 80–200 °C and 20–30 bar in several solvents, such as tetrahydrofuran, 2-propanol, water and in solventless conditions using 1:1 mass ratio of vanillin to guaiacol. The results revealed that the rate increased with increasing solvent polarity as follows: tetrahydrofuran < 2-propanol < water. The main product was
p
-creosol with 66% selectivity at complete vanillin conversion in HDO under 30 bar total pressure at 100 °C after 4 h using water as a solvent. In a solventless experiment with 1:1 mass ratio of vanillin–guaiacol as a feedstock only vanillin was transformed to
p
-creosol with 91% conversion in 4 h at 200 °C under 30 bar total pressure, while guaiacol did not produce any HDO products. Both thermodynamic analysis and kinetic modelling were performed. Vanillin hydrodeoxygenation resulted in formation of
p
-creosol over Pt/C catalyst using an optimum vanillin initial concentration in water solution. From the industrial point of view vanillin hydrodeoxygenation proceeded rapidly giving high yields of
p
-creosol in solventless hydrodeoxygenation of vanillin-guaiacol mixture, while guaiacol was not deoxygenated.
Graphical Abstract |
---|---|
ISSN: | 1011-372X 1572-879X |
DOI: | 10.1007/s10562-018-2478-1 |