Articles producció científica> Química Física i Inorgànica

Glycidol hydrogenolysis on a cheap mesoporous acid saponite supported Ni catalyst as alternative approach to 1,3-propanediol synthesis

  • Datos identificativos

    Identificador: PC:3201
    Autores:
    Salagre, P.Gebretsadik, F.B.Ruiz-Martinez, J.Cesteros, Y.
    Resumen:
    Filiació URV: SI
  • Otros:

    Autor según el artículo: Salagre, P.; Gebretsadik, F.B.; Ruiz-Martinez, J.; Cesteros, Y.
    Departamento: Química Física i Inorgànica
    Autor/es de la URV: SALAGRE CARNERO, MARÍA PILAR; Gebretsadik, F.B.; Ruiz-Martinez, J.; CESTEROS FERNÁNDEZ, YOLANDA
    Palabras clave: Glycidol Bifunctional catalysis Hydrogenolysis
    Resumen: This study explores the use of glycidol, as alternative to glycerol, to improve the selectively to 1,3-propanediol (PrD) by hydrogenolysis. The reaction was performed using Ni (with different Ni wt %) supported on an acid delaminated saponite catalysts which are cheaper compared to the expensive catalysts needed to favor the 1,3-PrD formation by glycerol hydrogenolysis. An increase in metallic area and a decrease in the catalyst acidity resulted in higher conversion and selectivity to propanediols (1,2- + 1,3-PrD). An acid activation of glycidol during hydrogenolysis promoted the 1,3-PrD formation and increased the 1,3-PrD/1,2-PrD ratio. For the catalyst prepared with 40 wt % Ni loading, an increase in the reaction temperature to 423 and 453 K led to higher 1,3-PrD/1,2-PrD ratio. The highest 1,3-PrD yield (29%) and 1,3-PrD/1,2-PrD ratio (0.97) at total conversion were obtained at 453 K, after 1 h. The overall 1,3-PrD yield from glycerol, assuming a two-step synthesis (Glycerol  Glycidol  1,3-PrD) and a yield of 78% for the first step, should be around 23%. This value is comparable to that reported for the hydrogenolysis of glycerol using noble metal catalysts.
    Grupo de investigación: Materials Catalítics en Química Verda
    Áreas temáticas: Química Química Chemistry
    Acceso a la licencia de uso: https://creativecommons.org/licenses/by/3.0/es/
    ISSN: 0926-860X
    Identificador del autor: 0000-0003-3257-2022; ; ; 0000-0002-5439-9358
    Fecha de alta del registro: 2018-03-15
    Página final: 98
    Volumen de revista: 538
    Versión del articulo depositado: info:eu-repo/semantics/submittedVersion
    Enlace a la fuente original: https://www.sciencedirect.com/science/article/pii/S0926860X17301175
    Programa de financiación: plan; CTQ2011-24610
    URL Documento de licencia: https://repositori.urv.cat/ca/proteccio-de-dades/
    DOI del artículo: 10.1016/j.apcata.2017.03.018
    Entidad: Universitat Rovira i Virgili
    Año de publicación de la revista: 2017
    Página inicial: 91
    Tipo de publicación: Article Artículo Article
  • Palabras clave:

    Catalitzadors
    Glicidol
    Glycidol
    Bifunctional catalysis
    Hydrogenolysis
    Química
    Química
    Chemistry
    0926-860X
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