Publications by authors named "Daniele Polidoro"

Palladium nanoparticles find extensive applications in catalysis in both homogeneously and heterogeneously catalyzed processes. Supporting metal nanoparticles enhances their stability as compared to their unsupported counterparts. The role of catalytic support is increasingly recognized as crucial in determining the behaviour of these materials.

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An efficient continuous-flow (CF) protocol was designed for the hydrogenation of lignin-derived aromatics to the corresponding cycloalkanes derivatives. A parametric analysis of the reaction was carried out by tuning the temperature, the H pressure and the flow rate, and using diphenyl ether (DPE) as a model substrate, commercial Ru/C as a catalyst, and isopropanol as a solvent: at 25 °C, 50 bar H , and a flow rate of 0.1 mL min , dicyclohexyl ether was achieved in an 86 % selectivity, at quantitative conversion.

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High anthropogenic CO emissions are among the main causes of climate change. Herein, we investigate the use of CO for the synthesis of organic cyclic carbonates on metal-free nitrogen-doped carbon catalysts obtained from chitosan, chitin, and shrimp shell wastes, both in batch and in continuous flow (CF). The catalysts were characterized by N physisorption, CO-temperature-programmed desorption, X-ray photoelectron spectroscopy, scanning electron microscopy, and CNHS elemental analysis, and all reactivity tests were run in the absence of solvents.

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Chitin, the second most abundant biopolymer in the planet after cellulose, represents a renewable carbon and nitrogen source. A thrilling opportunity for the valorization of chitin is focused on the preparation of biomass-derived -doped carbonaceous materials. In this contribution, chitin-derived -doped carbons were successfully prepared and functionalized with palladium metal nanoparticles.

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Three different multiphase systems (MP 1-3) comprised of two immiscible liquids, with or without an ionic liquid (IL: methyltrioctyl ammonium chloride), were investigated for the oxidation of 5-hydroxymethyl-furfural (HMF) over 5 % Ru/C as a catalyst and air (8 bar) as an oxidant. These conditions proved versatile for an excellent control of the reaction selectivity to 4 distinct products derived from full or partial oxidation of the carbonyl and alcohol functions of HMF, and each one achieved in 87-96 % isolated yield at complete conversion. MP1 based on water and isooctane, yielded 2,5-furandicarboxylic acid (FDCA, 91 % yield).

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