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The chemical recycling of used motor oil via catalytic cracking to convert it into secondary diesel-like fuels is a sustainable and technically attractive solution for managing environmental concerns associated with traditional disposal. In this context, this study was conducted to screen basic and acidic-aluminum silicate catalysts doped with different metals, including Mg, Zn, Cu, and Ni. The catalysts were thoroughly characterized using various techniques such as N2 adsorption–desorption isotherms, FT-IR spectroscopy, and TG analysis. The liquid and gaseous products were identified using GC, and their characteristics were compared with acceptable ranges from ASTM characterization methods for diesel fuel. The results showed that metal doping improved the performance of the catalysts, resulting in higher conversion rates of up to 65%, compared to thermal (15%) and aluminum silicates (≈20%). Among all catalysts, basic aluminum silicates doped with Ni showed the best catalytic performance, with conversions and yields three times higher than aluminum silicate catalysts. These findings significantly contribute to developing efficient and eco-friendly processes for the chemical recycling of used motor oil. This study highlights the potential of basic aluminum silicates doped with Ni as a promising catalyst for catalytic cracking and encourages further research in this area.

Solid phase extraction using magnetic nanoparticles has represented a leap forward in terms of the improvement of water quality, preventing the contamination of industrial effluents from discharge in a more efficient and affordable way. In the present work, superparamagnetic iron oxide nanoparticles (MNP) with different surface charges are tested as nanosorbents for the removal of chromium(VI) in aqueous solution. Uniform magnetic nanoparticles (~12 nm) were synthesized by a microwave polyol-mediated method, and tetraethyl orthosilicate (TEOS) and (3-aminopropyl) triethoxysilane (APTES) were grafted onto their surface, providing a variation in the surface charge. The adsorptive process of chromium was evaluated as a function of the pH, the initial concentration of chromium and contact time. Kinetic studies were best described by a pseudo-second order model in all cases. TEOS@MNP barely removed the chromium from the media, while non-grafted particles and APTES@TEOS@MNP followed the Langmuir model, with maximum adsorption capacities of 15 and 35 mgCr/g, respectively. The chromium adsorption capacities abruptly increased when the surface became positively charged as the species coexisting at the experimental pH are negatively charged. Furthermore, these particles have proven to be highly efficient in water remediation due their 100% reusability after more than six consecutive adsorption/desorption cycles., This research was funded by the Spanish Ministry of Economy and Competitiveness under grants MAT2017-88148-R, PGC2018-095642-B-I00 and Juan de la Cierva Formación FJCI-2015-23702.