Because of the growing demand for high-quality fuels, the light cycle oil fraction improvement including cetane number improvement is important. The main way to reach this improvement is the ring opening of cyclic hydrocarbons, and a highly effective catalyst should be found. Cyclohexane ring openings are a possible option to investigate the catalyst activity. In this work, we investigated rhodium-loaded catalysts prepared using the commercially available industrial supports: single-component ones, SiO₂ and Al₂O₃; and mixed oxides CaO + MgO + Al₂O₃ and Na₂O + SiO₂ + Al₂O₃. The catalysts were prepared by incipient wetness impregnation and investigated by N₂ low-temperature adsorption-desorption, XRD, XPS, DRS UV-Vis and DRIFT spectroscopy, SEM, and TEM with EDX. The catalytic tests were performed in cyclohexane ring opening in the range of 275–325 °C. The best result was demonstrated by the sample 1Rh/CaMgAlO: the selectivity to n-hexane was about 75% while the cyclohexane conversion was about 25% at 275 °C. The space-time yield was up to 12 mmol_n-hexane g_cat⁻¹h⁻¹.

The hydroconversion of asphaltenes into light hydrocarbons catalyzed by supported and free-standing non-noble metal nanoparticles was studied. The activity of Ni or Co immobilized on microspherical oxide carriers and Co nanoparticles dispersed in a hydrocarbon solution of asphaltene was found to be higher than that of a comparative Pt-Pd/Al₂O₃ catalyst. The yield of light products (C₅₊) reached up to 91% on cobalt nanoparticles supported onto alumina microspheres.