Catalytic converters contain the catalytic substance in their structure, which is a mixture of Platinum Group Metals (PGMs). The prices of these metals and a growing demand for them in the market, make it necessary to recycle spent catalytic converters and recovery of PGMs. In the study, the effect of ozone and hydrogen peroxide application on the possibility of extracting PGM from used car catalysts was investigated. The catalytic carrier was milled, sieved and then the fractions with the desired grain size were treated with the appropriate HCl mixture and 3%, 5%, 10%, 15% and 30% H2O2, respectively, and the tests were also carried out at temperature 333 K. Ozone tests were conducted with the O3 flow in the range of 1,3,5 g/h. Samples for analysis were collected after 30 min, 1 h, 2 h, 3 h and after 4 h, respectively. The residue after the experiments and filtration process was also analysed. The obtained results confirmed the assumption that PGMs can be extracted using hydrochloric acid with the addition of H2O2 or ozone as oxidants. It allows to significantly intensify the carried out reactions and to improve the rate of PGMs transfer to the solution.
New technologies and the globalization of the electrical and electronic equipment market cause a continuous increase in the amount of electrical and electronic waste. They constitute one of the waste groups that grows the fastest in quantity. The development of the new generation of electrical and electronic devices is much faster than before. Recently attention has been concentrated on hydrometallurgical methods for the recovery of metals from electronic waste. In this article the role of an oxidizing agent, mainly ozone and hydrogen peroxide was presented in hydrometallurgical processes. Leaching process of printed circuits boards (PCBs) from used cell phones was conducted. The experiments were carried out in the presence of sulfuric acid and ozone as an oxidizing agent for various temperatures, acid concentration, ozone concentration. As a result, the concentrations of copper, zinc, iron and aluminum in the obtained solution were measured. The obtained results were compared to results obtained earlier in the presence of hydrogen peroxide as an oxidizing agent and discussed.