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Relevant aspects of the conversion of guaiacol as a model compound for bio-oil over supported molybdenum oxycarbide catalysts
Molybdenum supported over activated carbon has been carburized under carbothermal hydrogen reduction conditions at different temperatures in order to modify the carburization degree. The resulting catalysts were characterized by N 2 physisorption, CO chemisorption, XPS, TPR, and TPD-NH 3 and compare...
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Published in: | New journal of chemistry 2020-07, Vol.44 (28), p.1227-1235 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Molybdenum supported over activated carbon has been carburized under carbothermal hydrogen reduction conditions at different temperatures in order to modify the carburization degree. The resulting catalysts were characterized by N
2
physisorption, CO chemisorption, XPS, TPR, and TPD-NH
3
and compared in the hydrodeoxygenation of guaiacol in a batch reactor as a lignin-derived model compound. The results have shown that the CO produced during the TPR could be related to the CO chemisorbed and the carburization degree of the material. The carburization degree was shown to increase with the final temperature, and under such conditions, two different Mo species, Mo
4+
and Mo
3+
, were identified in the oxycarbide phase. Catalytic results showed that the Mo
2
C is less active than the oxycarbide MoO
x
C
y
phase. Mo
2
C showed to improvement in the transalkylation reactions while in the case of MoO
x
C
y
, Mo
4+
promotes the hydrogenolysis of catechol to benzene while the Mo
3+
species was shown to activate hydrogenation reactions.
Molybdenum supported over activated carbon has been carburized under carbothermal hydrogen reduction conditions at different temperatures in order to modify the carburization degree and evaluated for guaiacol conversion. |
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ISSN: | 1144-0546 1369-9261 |
DOI: | 10.1039/d0nj02531c |