<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>8(45)</volume><submitter>Calzada LA</submitter><pubmed_abstract>The influence of the acid sites in the hydrodeoxygenation of anisole performed over Ni catalysts supported on SBA-15 modified with metal oxides (Ni/M-SBA-15, M = Ti, Zr, Al, or Nb) was demonstrated. Catalysts were characterized by SEM-EDX, nitrogen physisorption, XRD, UV-visible DRS, TPR, TPD of ammonia, IR-Py, O&lt;sub>2&lt;/sub> chemisorption, and high-resolution transmission electron microscopy. The mesoporous structure and the hexagonal arrangement of the supports were maintained in the catalysts. Ni catalysts supported on modified M-SBA-15 exhibited a higher metal-support interaction, an increase in the acidity and, as a consequence, improved selectivity to cyclohexane. The deoxygenation reaction rate constants increased as Ni/SBA-15 &lt; Ni/Ti-SBA-15 &lt; Ni/Nb-SBA-15 &lt; Ni/Zr-SBA-15 &lt; Ni/Al-SBA-</pubmed_abstract><journal>ACS omega</journal><pagination>42849-42866</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10652737</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Boosting the Hydrodeoxygenation Activity and Selectivity of Ni/(M)-SBA-15 Catalysts by Chemical Alteration of the Support.</pubmed_title><pmcid>PMC10652737</pmcid><pubmed_authors>Calzada LA</pubmed_authors><pubmed_authors>Sanchez-Ramirez M</pubmed_authors><pubmed_authors>Gomez-Cortes A</pubmed_authors><pubmed_authors>Klimova TE</pubmed_authors><pubmed_authors>Perez-Estrada D</pubmed_authors><pubmed_authors>Diaz G</pubmed_authors><pubmed_authors>Gomora-Herrera D</pubmed_authors></additional><is_claimable>false</is_claimable><name>Boosting the Hydrodeoxygenation Activity and Selectivity of Ni/(M)-SBA-15 Catalysts by Chemical Alteration of the Support.</name><description>The influence of the acid sites in the hydrodeoxygenation of anisole performed over Ni catalysts supported on SBA-15 modified with metal oxides (Ni/M-SBA-15, M = Ti, Zr, Al, or Nb) was demonstrated. Catalysts were characterized by SEM-EDX, nitrogen physisorption, XRD, UV-visible DRS, TPR, TPD of ammonia, IR-Py, O&lt;sub>2&lt;/sub> chemisorption, and high-resolution transmission electron microscopy. The mesoporous structure and the hexagonal arrangement of the supports were maintained in the catalysts. Ni catalysts supported on modified M-SBA-15 exhibited a higher metal-support interaction, an increase in the acidity and, as a consequence, improved selectivity to cyclohexane. The deoxygenation reaction rate constants increased as Ni/SBA-15 &lt; Ni/Ti-SBA-15 &lt; Ni/Nb-SBA-15 &lt; Ni/Zr-SBA-15 &lt; Ni/Al-SBA-</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Nov</publication><modification>2025-04-05T00:24:31.886Z</modification><creation>2025-04-05T00:24:31.886Z</creation></dates><accession>S-EPMC10652737</accession><cross_references><pubmed>38024772</pubmed><doi>10.1021/acsomega.3c05865</doi></cross_references></HashMap>