Evaluation of several catalytic systems for the epoxidation of methyl oleate using H 2O 2 as oxidant

  1. De Torres, M. 3
  2. Jiménez-Osés, G. 2
  3. Mayoral, J.A. 3
  4. Pires, E. 3
  5. Blanco, R.M. 1
  6. Fernández, O. 1
  1. 1 Instituto de Catálisis y Petroleoquímica
    info

    Instituto de Catálisis y Petroleoquímica

    Madrid, España

    ROR https://ror.org/004swtw80

  2. 2 University of California Los Angeles
    info

    University of California Los Angeles

    Los Ángeles, Estados Unidos

    ROR https://ror.org/046rm7j60

  3. 3 Universidad de Zaragoza
    info

    Universidad de Zaragoza

    Zaragoza, España

    ROR https://ror.org/012a91z28

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Revista:
Catalysis Today

ISSN: 0920-5861

Año de publicación: 2012

Volumen: 195

Número: 1

Páginas: 76-82

Tipo: Artículo

DOI: 10.1016/J.CATTOD.2012.05.005 SCOPUS: 2-s2.0-84868197343 WoS: WOS:000310570300010 GOOGLE SCHOLAR

Otras publicaciones en: Catalysis Today

Resumen

The interest of epoxidation of fatty esters lies in the production of renewable and biodegradable intermediates. A plethora of epoxidizing conditions have been reported in the literature, but it remains difficult to evaluate their relative efficiency and sustainability. To this aim, we present here an evaluation of several catalytic systems for the epoxidation of methyl oleate, together with a green metrics study using atom economy (AE), reaction mass efficiency (RME), material recovery parameter (MRP), yield and reaction time as main parameters. This study reveals the distinct efficiency of the fatty ester epoxidation systems presented in this work. The use of hydrogen peroxide (H 2O 2) together with fluorinated solvents and aryldiselenide compounds as catalysts was found to be the most efficient methodology. Enzymatic epoxidation also arises as an efficient alternate way to obtain methyl 9,10-epoxystearate. CALB immobilized onto silica has shown a good activity and improved recyclability with respect to Novozym 435. © 2012 Elsevier B.V.