In this paper, evidence is provided that the model reaction of aqueous dihydroxyacetone (DHA) conversion is as sensitive to the TiO catalysts' basicity as to their acidity. Two parallel pathways transformed DHA: while the pathway catalyzed by Lewis acid sites gave pyruvaldehyde (PA) and lactic acid (LA), the base-catalyzed route afforded fructose. This is demonstrated on a series of six commercial TiO samples and further confirmed by using two reference catalysts: niobic acid (NbOH), an acid catalyst, and a hydrotalcite (MgAlO), a basic catalyst.
View Article and Find Full Text PDFThis review article highlights part of the research activity of the C'Durable team at IRCELYON in the field of sustainable chemistry. This review presents a landscape of the work performed on the valorization of lignocellulosic biopolymers. These studies intend to transform cellulose, hemicellulose and lignin into valuable molecules.
View Article and Find Full Text PDFThe 'bottom-up' synthesis of homogeneously doped metal oxide nanoparticles (NPs) with precision at the atomic/molecular level offers many advantages. We report here the synthesis, structural characterization and hydrolytic behavior of new N-methyldiethanolamine-modified precursors of Ti(iv), Nb(v) and Pb(ii) and their application as excellent sol-gel precursors for obtaining atomically dispersed Nb and Pb within TiO2 having high surface areas (253-355 m2 g-1) and tunable acidic properties. Preliminary results on the use of these doped TiO2 as water-tolerant catalysts in transforming dihydroxyacetone to lactic acid are presented.
View Article and Find Full Text PDFAu(SG) (SG - glutathione) clusters deposited on ZrO nanoparticles have been used as a catalyst for benzyl alcohol oxidation. Calcination was performed at different temperatures to study the ligand and particle size effect on the catalytic activity. In contrast to most gold nanoclusters which have to be completely defunctionalized for maximum catalytic activity, the partially defunctionalized Au(SG)@ZrO catalyst, thermally treated at 300 °C, exhibits full conversion of benzyl alcohol within 15 h under atmospheric pressure with 94% selectivity towards benzaldehyde.
View Article and Find Full Text PDFThis article reports a detailed study on the reactivity of levulinic acid and cellulose with 1-butene and iso-butene for the catalytic formation of sec- and tert-butyl levulinates. The influence of catalyst type and various solvent conditions have been investigated to assess the potential of a sustainable transformation. A very simple and efficient procedure was discovered by using reusable Amberlyst-15 in the absence of solvent to form, from levulinic acid and iso-butene, tert-butyl levulinate (70 % yield), a compound very difficult to prepare by other means.
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