Landfilled metallurgical residues are valuable raw materials for the recovery of strategic vanadium resources. However, efficient separation of vanadium from these residues is challenging due to its strong oxidation resistance and coating within silicate inclusions. To address this issue, this study proposes an enhanced leaching process utilizing the synergistic effect of O₃-catalyzed ultrasonic field in a low concentration sulfuric acid system. Results show that following a 10-minute O₃ and ultrasonic treatment, the direct leaching rate of vanadium experienced a remarkable 46.7 % increase. Quenching experiments revealed a hierarchical order of active species within the reaction process:⋅OH >⋅O₂^-> H⁺, with⋅OH oxidation exhibiting the most pronounced capacity for disrupting the inclusion structure. Electron Paramagnetic Resonance analysis indicated that the highest⋅OH yield arose from the combined application of ultrasound and ozone. Kinetic investigations demonstrated that the vanadium leaching process is governed by interfacial chemical reactions. The activation energy of vanadium oxidation leaching under ultrasonic-O₃ conditions was determined to be 40.41 kJ/mol, representing a 20.19 % reduction compared to ultrasonic conditions alone. Through the integration of analysis, characterization, and comparative evaluations, it was discerned that the synergistic impact of ultrasonic and ozone treatments significantly enhances the breakdown of silicate inclusions by low-concentration HF, particularly in the conversion of SiOSi bonds into SiOH bonds and SiF bonds. In summary, the refined leaching methodology incorporating ozone catalysis in conjunction with ultrasonic treatment provides a new idea for the separation and extraction of refractory residual vanadium.

The aluminum hydroxide produced by the Bayer process contains a large amount of water which leads to the consumption of a large amount of heat for moisture removal in the calcination process, resulting in an increased energy consumption. The effects of temperature and microwave power on the dehydration ratio and the dry matter ratio of aluminum hydroxide were investigated. The characteristics of temperature variation during drying were discussed. X-ray diffraction (XRD), scanning electron microscopy (SEM), laser particle size, Fourier transform infrared (FTIR) spectroscopy, and dielectric property analyses were made to characterize the dried materials. The analysis results showed that within the range of bench-scale experimental parameters, the dehydration ratio was higher and the proportion of dry matter was lower at a higher final temperature. Within the range of pilot-scale experimental parameters, the dehydration ratio increased with the increasing microwave power from 500 W to 1500 W. XRD spectra revealed that when the final temperature exceeded 220 °C, a part of the aluminum hydroxide underwent a low-temperature phase transition to boehmite. The SEM images and a particle size analysis showed that there was no significant difference between the morphologies of the powder obtained by microwave drying and conventional drying methods. The powder obtained by both processes had an average particle size of around 80 μm. The dielectric constant and the dielectric loss of the dried material decreased greatly.