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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...

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Autores principales: Fangkoch, Sisira, Boonkum, Sutida, Ratchahat, Sakhon, Koo-amornpattana, Wanida, Eiad-Ua, Apiluck, Kiatkittipong, Worapon, Klysubun, Wantana, Srifa, Atthapon, Faungnawakij, Kajornsak, Assabumrungrat, Suttichai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
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
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author Fangkoch, Sisira
Boonkum, Sutida
Ratchahat, Sakhon
Koo-amornpattana, Wanida
Eiad-Ua, Apiluck
Kiatkittipong, Worapon
Klysubun, Wantana
Srifa, Atthapon
Faungnawakij, Kajornsak
Assabumrungrat, Suttichai
author_facet Fangkoch, Sisira
Boonkum, Sutida
Ratchahat, Sakhon
Koo-amornpattana, Wanida
Eiad-Ua, Apiluck
Kiatkittipong, Worapon
Klysubun, Wantana
Srifa, Atthapon
Faungnawakij, Kajornsak
Assabumrungrat, Suttichai
author_sort Fangkoch, Sisira
collection PubMed
description [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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spelling pubmed-71146072020-04-03 Solvent-Free Hydrodeoxygenation of Triglycerides to Diesel-like Hydrocarbons over Pt-Decorated MoO(2) Catalysts Fangkoch, Sisira Boonkum, Sutida Ratchahat, Sakhon Koo-amornpattana, Wanida Eiad-Ua, Apiluck Kiatkittipong, Worapon Klysubun, Wantana Srifa, Atthapon Faungnawakij, Kajornsak Assabumrungrat, Suttichai ACS Omega [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. American Chemical Society 2020-03-23 /pmc/articles/PMC7114607/ /pubmed/32258932 http://dx.doi.org/10.1021/acsomega.0c00326 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Fangkoch, Sisira
Boonkum, Sutida
Ratchahat, Sakhon
Koo-amornpattana, Wanida
Eiad-Ua, Apiluck
Kiatkittipong, Worapon
Klysubun, Wantana
Srifa, Atthapon
Faungnawakij, Kajornsak
Assabumrungrat, Suttichai
Solvent-Free Hydrodeoxygenation of Triglycerides to Diesel-like Hydrocarbons over Pt-Decorated MoO(2) Catalysts
title Solvent-Free Hydrodeoxygenation of Triglycerides to Diesel-like Hydrocarbons over Pt-Decorated MoO(2) Catalysts
title_full Solvent-Free Hydrodeoxygenation of Triglycerides to Diesel-like Hydrocarbons over Pt-Decorated MoO(2) Catalysts
title_fullStr Solvent-Free Hydrodeoxygenation of Triglycerides to Diesel-like Hydrocarbons over Pt-Decorated MoO(2) Catalysts
title_full_unstemmed Solvent-Free Hydrodeoxygenation of Triglycerides to Diesel-like Hydrocarbons over Pt-Decorated MoO(2) Catalysts
title_short Solvent-Free Hydrodeoxygenation of Triglycerides to Diesel-like Hydrocarbons over Pt-Decorated MoO(2) Catalysts
title_sort solvent-free hydrodeoxygenation of triglycerides to diesel-like hydrocarbons over pt-decorated moo(2) catalysts
url 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
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