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Solvent-Free Hydrodeoxygenation of Triglycerides to Diesel-like Hydrocarbons over Pt-Decorated MoO(2) Catalysts
[Image: see text] In the present work, the solvent-free hydrodeoxygenation of palm oil as a representative triglyceride model compound to diesel-like hydrocarbons was evaluated in a batch reactor using Pt-decorated MoO(2) catalysts. The catalysts with various Pt loadings (0.5–3%) were synthesized by...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7114607/ https://www.ncbi.nlm.nih.gov/pubmed/32258932 http://dx.doi.org/10.1021/acsomega.0c00326 |
Sumario: | [Image: see text] In the present work, the solvent-free hydrodeoxygenation of palm oil as a representative triglyceride model compound to diesel-like hydrocarbons was evaluated in a batch reactor using Pt-decorated MoO(2) catalysts. The catalysts with various Pt loadings (0.5–3%) were synthesized by an incipient wetness impregnation method. The metallic Pt and MoO(2) phases were detected in the XRD patterns of as-prepared catalysts after the reaction and acted as active components for the deoxygenation reactions. The XPS experiments confirmed the existence of metallic Pt and PtO(x) species. The XANES investigation of Mo L(3)-edge spectra elucidated a change in the valence state by the transformation of MoO(3) into MoO(2) species after the deoxygenation reaction. The TEM observation revealed the formation of Pt nanoparticles in the range of 1–3 nm decorated on MoO(2) species. The number of acid sites increased with stronger metal–support interactions on increasing the Pt loading. The catalytic performance of the MoO(2) catalyst significantly improved with a small amount of Pt decoration. However, the further increase in Pt loading did not relatively increase the deoxygenation activity due to the formation of the agglomerated Pt particles. The high performance of the decorated catalysts could be attributed to the moderate acidity from the Pt dispersed on MoO(2) toward decarbonylation and decarboxylation reactions. |
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