6533b7dcfe1ef96bd1273499

RESEARCH PRODUCT

Synthesis of vanillin in water by TiO2 photocatalysis

Vincenzo AugugliaroLeonardo PalmisanoG. Camera-rodaMaria Angela PumaGiovanni PalmisanoVittorio LoddoFrancesco Parrino

subject

Titanium dioxide Photocatalysis Vanillin Partial oxidationSettore ING-IND/24 - Principi Di Ingegneria ChimicaChemistryFormic acidSettore ING-IND/25 - Impianti ChimiciTITANIUM DIOXIDEProcess Chemistry and TechnologyVanillinOxalic acidSubstrate (chemistry)Catalysischemistry.chemical_compoundVanillyl alcoholIsoeugenolAcetic acidSUSTAINABLE CHEMISTRYOrganic chemistryVANILLINSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePHOTOCATALYSISSelectivityTiO2 Selective oxidation VanillinGREEN CHEMISTRYGeneral Environmental Science

description

Abstract The photoproduction of vanillin is studied in aqueous medium starting from trans-ferulic acid, isoeugenol, eugenol or vanillyl alcohol by using both commercial and home prepared TiO2 samples as photocatalysts and batch Pyrex photoreactors. The photo-oxidation at room temperature of these compounds produces vanillin with a selectivity ranging from 1.4 to 21 mol% with respect to the converted substrate. An investigation on the intermediates was performed in the case of trans-ferulic acid; for this substrate the most important intermediates were homovanillic acid, vanillyl mandelic acid, trans-caffeic acid, formic acid, acetic acid, and oxalic acid. The carbon mass balance, including CO2 derived from the mineralization, was made for all of the substrates at irradiation times corresponding to the highest selectivity to vanillin. High closure of the carbon balance was obtained with vanillyl alcohol (ca. 90%) and trans-ferulic acid (ca. 80%).

https://doi.org/10.1016/j.apcatb.2011.11.007