Al-MIL-53 metal-organic framework supported Ru catalyst for selective hydrodeoxygenation of lignin-derived phenols into cyclohexane
- Authors
- Khani, Yasin; Kumar, Avnish; Bu, Sung Kang; Chang, Hyun Ko; Moonis, Ali Khan; Jeon, Byong-Hun; Park, Young-Kwon
- Issue Date
- Jun-2024
- Publisher
- Elsevier BV
- Keywords
- Cyclohexane; Guaiacol; Hydrodeoxygenation; Hydrogenation; Ru/Al-MIL −53
- Citation
- Chemical Engineering Journal, v.490, pp 1 - 15
- Pages
- 15
- Indexed
- SCIE
SCOPUS
- Journal Title
- Chemical Engineering Journal
- Volume
- 490
- Start Page
- 1
- End Page
- 15
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/195065
- DOI
- 10.1016/j.cej.2024.151637
- ISSN
- 1385-8947
1873-3212
- Abstract
- Catalytic hydrodeoxygenation (HDO) of guaiacol, as a bio-oil model compound, was investigated employing Ru/Al-MIL −53 Metal-Organic Framework and Ru/γ-Al2O3 catalysts under external molecular hydrogen. Notably, the HDO results attributed the remarkable potential of the Ru/Al-MIL −53 MOF toward the comparatively high conversion of guaiacol (70%) together with a high proportion of cyclohexanol (23%) at a catalyst/feed (C/F) ratio of 1:5. However, only a 30% conversion was found with only 3.5% cyclohexanol for Ru/γ-Al2O3 for the same C/F ratio. This was due to the high porosity and presence of numerous vacancies in the MOF, which directly affects the H2-dissociation/ spillover that assists the transfer of produced H-radicals for further conversion of the adsorbed guaiacol molecules. Notably, the activity of Ru/Al-MIL −53 was remarkably increased by decreasing the amount of guaiacol. The maximum conversion was achieved (100%) for a C/F ratio of 1:1, with a higher (96.2%) selectivity for cyclohexane. The reusability test for the spent catalyst did not show any significant change in catalyst performance for up to five successive cycles.
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