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Transfer hydrogenation (TH) is considered as one of the most promising ways to convert biomass into valuable products. This study aims to demonstrate the performance of high-loaded Ni-based catalysts in the TH of phenolic compounds such as guaiacol and dimethoxybenzenes. The experiments were carried out under supercritical conditions at 250 °C using 2-PrOH as the only hydrogen donor. Ni-SiO2 and NiCu-SiO2 were synthesized using the eco-friendly original method based on supercritical antisolvent coprecipitation. It has been found that guaiacol is rapidly converted into 2-methoxycyclohexanol and cyclohexanol, while the presence of Cu impedes the formation of the latter product. Transformations of dimethoxybenzene position isomers are slower and result in different products. Thus, 1,3-dimethoxybenzene loses oxygen atoms transform into methoxycyclohexane and cyclohexanol, whereas the saturation of the aromatic ring is more typical for other isomers. The Cu addition increases specific catalytic activity in the TH of 1,2-and 1,3-dimethoxybenzene compared to the Cu-free catalyst. [ABSTRACT FROM AUTHOR]

Mixed Ni-Al oxide catalytic precursors with different elemental ratios (20, 50, and 80 wt.% Ni0) were synthesized using green supercritical antisolvent co-precipitation (SAS). The obtained oxide precursors and metal catalysts were characterized in detail by X-ray diffraction (XRD) analysis, atomic pair distribution function (PDF) analysis, CO adsorption, and high-resolution transmission electron microscopy (HRTEM). It was found that the composition and structure of the Ni-Al precursors are related to the Ni content. The mixed Ni1−xAlxO oxide with NiO-based crystal structure was formed in the Ni-enriched sample, whereas the highly dispersed NiAl2O4 spinel was observed in the Al-enriched sample. The obtained metal catalysts were tested in the process of anisole H2-free hydrogenation. 2-PrOH was used as a hydrogen donor. The catalyst with 50 wt.% Ni0 demonstrated the highest activity in the hydrogenation process. [ABSTRACT FROM AUTHOR]

Binary Ni–Cu heterogeneous catalysts are known to demonstrate excellent activity in conventional hydrogenation of phenolic compounds, and Cu addition facilitates hydrodeoxygenation (HDO). In this study, we aimed to show the effect of Cu on the specific catalytic activity and selectivity of Ni–Cu catalysts in transfer hydrogenation, in which 2-PrOH was used as a solvent and an H donor. Catalytic transformations of anisole were studied in sub- and supercritical alcohol at 150 and 250 °C. The catalysts were prepared using an environmentally friendly supercritical antisolvent coprecipitation method, which makes it possible to obtain well-dispersed particles (less than 7 nm) at high metal loading (up to 50 wt.%). When copper is added, deactivation of the catalyst in transformations of anisole, including HDO, is observed. The experimental data and the appropriate kinetic analysis demonstrate that there is a decrease in the rate of anisole conversion accompanied by an increase in the concentration of acetone formed during the dehydrogenation of 2-PrOH. [ABSTRACT FROM AUTHOR]