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Due to population growth and industrial development consumption of non-renewable energy sources, and consequently pollution, has increased. In order to reduce energy utilisation and preserve the environment, developed and developing countries are increasingly trying to find solutions based on renewable energy sources. Cost-effective wastewater treatment methods using solar energy would significantly ensure effective water source utilisation, thereby contributing towards sustainable development goals. In this paper, special emphasis is given to the use of solar energy as the driving force of the process, as well as the use of highly active magnetic TiO2-based catalysts. Therefore, in this study, we investigated the possibility of photocatalytic degradation of aqueous magenta graphic dye using titanium dioxide as a catalyst and DSD model in order to achieve the best process optimisation. TiO2 was successfully coated with magnetic nanoparticles by one step process and characterized using different techniques (BET, SEM/EDS, FTIR, XRD). Based on DSD statistical method optimal reaction conditions were pH = 6.5; dye concentration 100 mg/L; TiO2–Fe3O4 0.6 g/L, at which the highest degree of magenta dye decolourisation was achieved (85%). Application of solar energy coupled with magnetic TiO2 catalyst which could be recovered and reused makes this approach a promising alternative in green wastewater treatment.

This research investigates the potential use of pyrite cinder (PC) as an efficient Fenton-like catalyst for the removal of the reactive azo dye Reactive Red 120 (RR120) from aqueous solutions. The characterization of its PC structure and composition confirmed its great potential to act as catalytic iron source in a heterogeneous Fenton system. Dye removal optimization was performed in terms of PC dosage (0.4–8 g/L), H2O2 concentration (2–25 mM), pH value (2–4.6), initial dye concentration (50–200 mg/L), and mixing time. The highest decolorization efficiency (92%) was achieved after a reaction time of 480 min under following conditions: RR120 = 50 mg/L, PC = 4 g/L, H2O2 = 10 mM, and pH = 3. After decolorization, an extensive analysis of the generated effluent was performed regarding metal leaching, mineralization, toxicity, and degradation product formation. The metal leaching indicated the necessity for a pH increase in order to remove the settled metal hydroxides. The mineralization efficiency was satisfactory, reaching 85% and 62% of the COD and TOC removal, respectively. The respirometry measurements and bioluminescence tests indicated the detoxification of the treated solution. The absorption spectra and GC/MS analysis confirmed the changes in the molecular structure in the form of the destruction of the azo bond, with a simpler aromatic and aliphatic intermediates formation. This study provides an effective method for removing azo dye in polluted water by employing waste tailings as alternative Fenton-like catalysts, while also using waste tailings as the secondary resource.