Zirconia-supported tungstophosphoric heteropolyacid as heterogeneous acid catalyst for biodiesel production

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Title: Zirconia-supported tungstophosphoric heteropolyacid as heterogeneous acid catalyst for biodiesel production
Authors: Alcañiz-Monge, Juan | El Bakkali, Bouchra | Trautwein, Guido | Reinoso, Santiago
Research Group/s: Materiales Carbonosos y Medio Ambiente
Center, Department or Service: Universidad de Alicante. Departamento de Química Inorgánica
Keywords: Immobilized heteropolyacid | Zirconia support | Textural properties | Palmitic acid esterification
Knowledge Area: Química Inorgánica
Issue Date: May-2018
Publisher: Elsevier
Citation: Applied Catalysis B: Environmental. 2018, 224: 194-203. doi:10.1016/j.apcatb.2017.10.066
Abstract: A series of materials based on the immobilization of the 12-tungstophosphoric heteropolyacid over zirconia supports have been prepared and applied as heterogeneous acid catalysts in the esterification of palmitic acid with methanol as a model reaction for the preliminary stage of the biodiesel production. The title materials have been obtained through the sol-gel method combined with a subsequent hydrothermal treatment at mild conditions, which affords catalysts with larger porosity and higher thermal and chemical stability under the esterification reaction conditions than other preparative approaches. Generating the zirconia support by hydrolysis of an alkoxyde precursor in the presence of the heteropolyacid leads to materials with homogeneously well-dispersed clusters, as well as to an increasing contribution of the tetragonal ZrO2 crystalline phase, a decreasing size of the nanoparticles and larger microporous volumes as the loading of the Keggin-type species increases. The 12-tungstophosphoric acid retains its catalytic activity in the esterification of palmitic acid with methanol at 60 °C upon immobilization over zirconia and conversions even higher than those observed under homogeneous conditions are obtained due to the active contribution of the support. The sample with a 30% mass percentage of heteropolyacid has been identified as the most efficient catalyst because it affords conversions above the 90% and shows the lower loss of activity over successive reaction runs among all of our materials. This loss of activity has been analyzed on the basis of the leaching of the catalyst and the fouling of the materials.
Sponsor: This work was financially supported by Generalitat Valenciana through FEDER funds (grant PROMETEO2/2014/010) and by the Spanish Ministerio de Economia y Competitividad (grant CTQ2015-64801-R). S.R. acknowledges financial support from InaMat and from the program “Ayudas para la Captación del Talento adscritas a los Institutos de Investigación de la UPNA” funded by a collaboration agreement with Obra Social la Caixa and Fundación Caja Navarra.
URI: http://hdl.handle.net/10045/72638
ISSN: 0926-3373 (Print) | 1873-3883 (Online)
DOI: 10.1016/j.apcatb.2017.10.066
Language: eng
Type: info:eu-repo/semantics/article
Rights: © 2017 Elsevier B.V.
Peer Review: si
Publisher version: http://dx.doi.org/10.1016/j.apcatb.2017.10.066
Appears in Collections:INV - MCMA - Artículos de Revistas

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