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    CO2 electro-valorization to dimethyl carbonate from methanol using potassium methoxide and the ionic liquid [bmim][Br] in a filter-press electrochemical cell

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    Identificadores
    URI: http://hdl.handle.net/10902/9845
    DOI: 10.1002/jctb.4445
    ISSN: 0268-2575
    ISSN: 1097-4660
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    Autoría
    García Herrero, María IsabelAutoridad Unican; Álvarez Guerra, ManuelAutoridad Unican; Irabien Gulías, ÁngelAutoridad Unican
    Fecha
    2015-08
    Derechos
    © Wiley. This is the peer reviewed version of the following article: J. Chem. Technol. Biotechnol, 2015, 90(8), 1433–1438, which has been published in final form at http://dx.doi.org/10.1002/jctb.4445. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.
    Publicado en
    Journal of Chemical Technology and Biotechnology, 2015, 90(8), 1433–1438
    Editorial
    Wiley-Blackwell
    Enlace a la publicación
    http://dx.doi.org/10.1002/jctb.4445
    Palabras clave
    Carbon dioxide
    Valorization
    Dimethyl carbonate
    Methanol
    Ionic liquid
    Filter-press cell
    Resumen/Abstract
    BACKGROUND: The electrochemical valorization of CO2 into added-value products appears a promising strategy for reducing CO2 emissions and mitigating climate change. Dimethyl carbonate (DMC) is an environmentally friendly valuable chemical, with multiple applications, and has been suggested as a potential gasoline additive. However, DMC has traditionally been produced from hazardous phosgene and CO routes, which encourages the interest in developing new processes. The aim of this work is to study the valorization process for the direct electrosynthesis of DMC from CO2 and methanol using CH3OK and the ionic liquid 1-butyl-3-methylimidazolium bromide, avoiding the addition of carcinogenic compounds. RESULTS: The evolution of the concentration of DMC was studied in a filter-press electrochemical cell with anodic and cathodic compartments separated by a Nafion 117 membrane, operating for 48 h. A final DMC concentration of 15.07 mmol L-1 was observed. Analysis of the by-products obtained in the process revealed the formation of tetramethyl orthocarbonate and dimethoxymethane, which were detected and quantified in the liquid phase. A simplified reaction scheme was also proposed based on the results obtained. CONCLUSION: Unlike all previous work that used an undivided cell, the new experimental results of this study using a divided cell can serve as a reference for further research to overcome current limitations.
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    UNIVERSIDAD DE CANTABRIA

    Repositorio realizado por la Biblioteca Universitaria utilizando DSpace software
    Contacto | Sugerencias
    Metadatos sujetos a:licencia de Creative Commons Reconocimiento 4.0 España