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Prof. Sivanesan Subramanian

Anna University, India

 

Prof. Hassan Karimi-Maleh

University of Electronic Science
and Technology of China (UESTC)

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Home > Archives > Vol 5, No 1 (Published) > Original Research Article
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2022-04-28

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Vol 5, No 1 (Published)

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Original Research Article

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How to Cite

Puello-Polo, E., Santiago, W. M., Hernández, B. M., Ramos, V. S., & Arrieta, A. A. (2022). Effect of vulcanization and reaction temperature of the carbide supported on activated carbon on glycerol trioleate deoxygenation. Applied Chemical Engineering, 5(1), 70–79. https://doi.org/10.24294/ace.v5i1.1450
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Effect of vulcanization and reaction temperature of the carbide supported on activated carbon on glycerol trioleate deoxygenation

Esneyder Puello-Polo

Universidad del Atlántico

Wendy Martinez Santiago

Universidad del Atlántico

Brando Martínez Hernández

Universidad del Atlántico

Vanessa Sarmiento Ramos

Universidad del Atlántico

Alberto Albis Arrieta

Universidad del Atlántico


DOI: https://doi.org/10.24294/ace.v5i1.1450


Keywords: Sulfidation, CoMo/CA Carbide, Deoxygenation, Glyceryl Trioleate, HDO, HDC


Abstract

Cobalt molybdenum carbide supported on activated carbon was synthesized and the effect of sulfiding on the catalytic activity of the glycerol trioleate deoxygenation process (DOX) was evaluated. Prior to the glycerol trioleate deoxygenation reactions, the catalyst was reduced and sulfided with CS2/H2. The CoMo/CA carbide was characterized by specific area (B.E.T), X-ray diffraction (XRD), elemental analysis (CHON-S), potentiometric titration with n-butylamine and X-ray photoelectron spectroscopy (XPS). The specific area of the CoMo/CA carbide and the support were 246 m2/g and 881 m2/g, respectively. XRD analysis proved the presence of Co6Mo6C2 and metallic cobalt. XPS showed the presence on the surface of signals assignable to Moδ+, Mo4+, Mo6+, Co2+, S2– and SO42–. Sulfided CoMo/CA carbide showed higher activad to glycerol trioleate esoxygenation than unsulfided CoMo/CA carbide. The highest yield was obtained at 310 °C, 900 psi H2 and 2 h of reaction (100% conversion) and a higher selectivity towards heptadecane (55%) and octadecane (45%) favoring decarboxylation (HDCX) and decarbonylation (HDCn) than hydrodeoxygenation (HDO).


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