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Eco-Friendly Transformation of Bioethanol into Ethylene over Bimetallic Nickel-Copper Catalysts.
Gaitán Chavarría, Emily; Picado Espinoza, Thamara; Durán Herrera, Esteban; Miranda Morales, Bárbara Cristina.
Afiliação
  • Gaitán Chavarría E; Chemical Engineering School, Universidad de Costa Rica, San José, 2060, Costa Rica.
  • Picado Espinoza T; Chemical Engineering School, Universidad de Costa Rica, San José, 2060, Costa Rica.
  • Durán Herrera E; Chemical Engineering School, Universidad de Costa Rica, San José, 2060, Costa Rica.
  • Miranda Morales BC; Chemical Engineering School, Universidad de Costa Rica, San José, 2060, Costa Rica.
Chempluschem ; : e202400135, 2024 Jul 04.
Article em En | MEDLINE | ID: mdl-38963686
ABSTRACT
The conversion of bioethanol to ethylene in gas phase and atmospheric pressure was investigated over γ-Al2O3 supported copper and nickel catalysts. These catalysts were prepared by co-precipitation and pre-treated with hydrogen at 450 °C. Six catalysts were studied at 450 °C under a nitrogen atmosphere. It was found that the monometallic Cu/γ-Al2O3 catalyst exhibited the highest ethylene concentration, with a selectivity of around 90 %. The bioethanol conversion obtained was between 57 %-86 %. Another catalyst that exhibited high concentration values was the NiCu1 7 bimetallic catalyst. The catalysts were characterised using XRD, SEM, EDS, TEM, TGA, FTIR, Raman, and N2-physisoption techniques. Furthermore, the Cu/γ-Al2O3 catalyst was studied under different reduction temperatures and gas flow conditions. It was found that the catalysts reduced at 350 °C and 35 ml/min N2 flow presented ethylene concentrations between (0.18-0.21) g/L. Moreover, the catalyst deactivation was identified to be first order and the equation of the Cu/γ-Al2O3 catalyst deactivation model was determined. Carbonaceous deposits over the used sample were not detected by Raman and FTIR. It was determined that the Cu/γ-Al2O3 catalyst deactivation could be mainly attributed to the blocking of the catalytic sites by strongly adsorbed compounds and hydroxylation of the catalyst surface.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chempluschem Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Costa Rica País de publicação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Chempluschem Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Costa Rica País de publicação: Alemanha