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Solvent-Free Hydrodeoxygenation of Triglycerides to Diesel-like Hydrocarbons over Pt-Decorated MoO2 Catalysts.
Fangkoch, Sisira; Boonkum, Sutida; Ratchahat, Sakhon; Koo-Amornpattana, Wanida; Eiad-Ua, Apiluck; Kiatkittipong, Worapon; Klysubun, Wantana; Srifa, Atthapon; Faungnawakij, Kajornsak; Assabumrungrat, Suttichai.
Afiliação
  • Fangkoch S; Department of Chemical Engineering, Faculty of Engineering, Mahidol University, Nakhon Pathom 73170, Thailand.
  • Boonkum S; Department of Chemical Engineering, Faculty of Engineering, Mahidol University, Nakhon Pathom 73170, Thailand.
  • Ratchahat S; Department of Chemical Engineering, Faculty of Engineering, Mahidol University, Nakhon Pathom 73170, Thailand.
  • Koo-Amornpattana W; Department of Chemical Engineering, Faculty of Engineering, Mahidol University, Nakhon Pathom 73170, Thailand.
  • Eiad-Ua A; College of Nanotechnology, King Mongkut's Institute of Technology Ladkrabang, Bangkok 10520, Thailand.
  • Kiatkittipong W; Department of Chemical Engineering, Faculty of Engineering and Industrial Technology, Silpakorn University, Nakhon Pathom 73000, Thailand.
  • Klysubun W; Synchrotron Light Research Institute, Nakhon Ratchasima 30000, Thailand.
  • Srifa A; Department of Chemical Engineering, Faculty of Engineering, Mahidol University, Nakhon Pathom 73170, Thailand.
  • Faungnawakij K; National Nanotechnology Center (NANOTEC), National Science and Technology Development Agency, Pathum Thani 12120, Thailand.
  • Assabumrungrat S; Center of Excellence in Catalysis and Catalytic Reaction Engineering, Department of Chemical Engineering, Faculty of Engineering, Chulalongkorn University, Bangkok 10330, Thailand.
ACS Omega ; 5(12): 6956-6966, 2020 Mar 31.
Article em En | MEDLINE | ID: mdl-32258932
ABSTRACT
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 MoO2 catalysts. The catalysts with various Pt loadings (0.5-3%) were synthesized by an incipient wetness impregnation method. The metallic Pt and MoO2 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 L3-edge spectra elucidated a change in the valence state by the transformation of MoO3 into MoO2 species after the deoxygenation reaction. The TEM observation revealed the formation of Pt nanoparticles in the range of 1-3 nm decorated on MoO2 species. The number of acid sites increased with stronger metal-support interactions on increasing the Pt loading. The catalytic performance of the MoO2 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 MoO2 toward decarbonylation and decarboxylation reactions.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ACS Omega Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Tailândia

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: ACS Omega Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Tailândia