Conditions Extrêmes et Matériaux : Haute Température et Irradiation
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2016

ACL
doi

A.M.E.Caicedo, J.A.Rengifo-Herrera, P.Florian, M.N.Blanco, G.P.Romanelli, L.R.Pizzio, 'Valorization of biomass derivatives: Keggin heteropolyacids supported ontitania as catalysts in the suitable synthesis of2-phenoxyethyl-2-furoate', J. Mol. Cat. A: Chemical 425 266-274 (2016) doi:10.1016/j.molcata.2016.10.024

Titania modified by tungstophosphoric (TPA) and tungstosilicic (TSA) acid (30% w/w) were synthesized by the sol-gel method, using urea as low cost pore-forming agent and annealing at 500 degrees C for 2h (TiO2/TPA and TiO2/TSA respectively). The obtained materials were characterized by P-31, (29)si, H-1 nuclear magnetic resonance (31P, Si-29, H-1 MAS-NMR), X-ray diffraction (XRD), X-ray photo-electron spectroscopy (XPS), Raman spectroscopy (FT-Raman), acid strength by potentiometric titration with n-butylamine. Mesoporous materials were obtained, without important microporosity, as determined from N-2 adsorption-desorption isotherms by the Brunauer-Emmett-Teller (BET) method. The XRD patterns of the modified samples exhibited only peaks of anatase phase. According P-31/Si-29 MAS-NMR and XPS studies, the main species present in the TiO2/TPA and TiO2/TSA samples are the Keggin anions by forming surface acid species, and probably surface complex between Keggin anion and titania as well. Solids were evaluated in the synthesis of 2-phenoxyethyl-2-furoate, by esterification of 2-furoic acid, a valuable product which can be obtained from biomass, with 2-phenoxyethanol, where TiO2/TPA sample showed the highest catalytic activity. The reaction temperature, molar ratio acid:alcohol and catalyst amount were studied as variables using TiO2/TPA sample. Results of catalytic activity and diffuse reflectance infrared Fourier transform spectroscopy (DRIFT-Fr-IR) measurements suggested that the reaction mechanism may involve a protonated intermediate of 2-furoic acid polarizing the C=O bond of the acid, and leaving that can be easily attacked by 2-phenoxyethanol. (C) 2016 Elsevier B.V. All rights reserved.