Abstract
The hydrodeoxygenation of lignin monomer guaiacol via catalytic transfer hydrogenation was studied with 2-propanol as a hydrogen donor and Ru-based catalysts. Guaiacol was mainly converted into a partially deoxygenated product, cyclohexanol (> 70% selectivity), over Ru/C catalysts with the hydrogen produced in-situ from 2-propanol. An addition of Re to Ru/C catalysts significantly enhanced the rate of C—O hydrogenolysis, resulting in the complete deoxygenation to cyclohexane (~ 60% selectivity). The remarkable deoxygenation ability of the bimetallic RuRe/C catalyst is attributed to its bifunctional characteristic, by which Ru catalyzes the hydrogenation-hydrogenolysis of guaiacol and Re provides acid sites to promote cyclohexane production via hydrogenolysis.
| Original language | English |
|---|---|
| Pages (from-to) | 113-118 |
| Number of pages | 6 |
| Journal | Catalysis Communications |
| Volume | 86 |
| DOIs | |
| Publication status | Published - 2016 Nov 5 |
Bibliographical note
Funding Information:This work was supported by the New & Renewable Energy Core Technology Program of the Korea Institute of Energy Technology Evaluation and Planning (KETEP) granted financial resource from the Ministry of Trade, Industry and Energy , Republic of Korea (No. 20153030101580 ). This research was also supported by the National Research Council of Science & Technology (NST) grant by the Korea government ( MSIP ) (No. CAP-11-04-KIST ). The authors also appreciate further support by the Korea Institute of Science and Technology (KIST) Institutional Program ( 2E26550 ).
Publisher Copyright:
© 2016 Elsevier B.V.
Keywords
- Bimetallic
- Biomass
- Guaiacol
- RuRe
- Transfer hydrogenation
ASJC Scopus subject areas
- Catalysis
- General Chemistry
- Process Chemistry and Technology
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