<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(30)</volume><submitter>Mukundan S</submitter><funding>University of Queensland</funding><pubmed_abstract>NiMoS&lt;sub>2&lt;/sub> nanoparticles supported on carbon, synthesized by a microemulsion method were used as a nanocatalyst for hydrodeoxygenation (HDO) of a lignin model compound - guaiacol. Two types of carbon supports - mesoporous carbon (CMK-3) and activated carbon (AC) with a predominantly microporous structure, were studied to investigate the role of porosity and nature of the porous structure in catalyst activity. The activity of NiMoS&lt;sub>2&lt;/sub>/AC resulted in the complete guaiacol conversion at 13 h of reaction time to produce phenol (31.5 mol%) and cyclohexane (35.7 mol%) as the two main products. Contrastingly, NiMoS&lt;sub>2&lt;/sub>/CMK-3 needed a much lesser reaction time (6 h) to attain a similar conversion of guaiacol but gave different selectivities of phenol (25 mol%) and cyclohexane (55.5 mol%). Increased cyclohexane production with NiMoS&lt;sub>2&lt;/sub>/CMK-3 implied better deoxygenation of MoS&lt;sub>2&lt;/sub> and enhanced hydrogenation capacity of Ni since phenol is a partially deoxygenated product of guaiacol while cyclohexane is a completely deoxygenated and hydrogenated product. The superior catalytic activity and deoxygenating behavior of NiMoS&lt;sub>2&lt;/sub>/CMK-3 catalysts could be attributed to the organized mesoporosity of the CMK-3 support in relation to the improved active phase distribution and access to active sites that facilitate the conversion of the reaction's product. Recyclability study implied NiMoS&lt;sub>2&lt;/sub>/CMK-3 was more stable without significant changes in the catalytic activity even after three reaction cycles.</pubmed_abstract><journal>RSC advances</journal><pagination>17194-17202</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9064553</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Highly active and robust Ni-MoS&lt;sub>2&lt;/sub> supported on mesoporous carbon: a nanocatalyst for hydrodeoxygenation reactions.</pubmed_title><pmcid>PMC9064553</pmcid><pubmed_authors>Mukundan S</pubmed_authors><pubmed_authors>Konarova M</pubmed_authors><pubmed_authors>Beltramini J</pubmed_authors><pubmed_authors>Wahab MA</pubmed_authors><pubmed_authors>Atanda L</pubmed_authors></additional><is_claimable>false</is_claimable><name>Highly active and robust Ni-MoS&lt;sub>2&lt;/sub> supported on mesoporous carbon: a nanocatalyst for hydrodeoxygenation reactions.</name><description>NiMoS&lt;sub>2&lt;/sub> nanoparticles supported on carbon, synthesized by a microemulsion method were used as a nanocatalyst for hydrodeoxygenation (HDO) of a lignin model compound - guaiacol. Two types of carbon supports - mesoporous carbon (CMK-3) and activated carbon (AC) with a predominantly microporous structure, were studied to investigate the role of porosity and nature of the porous structure in catalyst activity. The activity of NiMoS&lt;sub>2&lt;/sub>/AC resulted in the complete guaiacol conversion at 13 h of reaction time to produce phenol (31.5 mol%) and cyclohexane (35.7 mol%) as the two main products. Contrastingly, NiMoS&lt;sub>2&lt;/sub>/CMK-3 needed a much lesser reaction time (6 h) to attain a similar conversion of guaiacol but gave different selectivities of phenol (25 mol%) and cyclohexane (55.5 mol%). Increased cyclohexane production with NiMoS&lt;sub>2&lt;/sub>/CMK-3 implied better deoxygenation of MoS&lt;sub>2&lt;/sub> and enhanced hydrogenation capacity of Ni since phenol is a partially deoxygenated product of guaiacol while cyclohexane is a completely deoxygenated and hydrogenated product. The superior catalytic activity and deoxygenating behavior of NiMoS&lt;sub>2&lt;/sub>/CMK-3 catalysts could be attributed to the organized mesoporosity of the CMK-3 support in relation to the improved active phase distribution and access to active sites that facilitate the conversion of the reaction's product. Recyclability study implied NiMoS&lt;sub>2&lt;/sub>/CMK-3 was more stable without significant changes in the catalytic activity even after three reaction cycles.</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 May</publication><modification>2025-04-05T13:24:06.952Z</modification><creation>2025-04-05T13:24:06.952Z</creation></dates><accession>S-EPMC9064553</accession><cross_references><pubmed>35519874</pubmed><doi>10.1039/c9ra02143d</doi></cross_references></HashMap>