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This study focused on the degradation of hydrolysed Remazol Black B (CI Reactive Black 5), a common diazo reactive dye, in aqueous solution. In the presence of various dye auxiliary chemicals a typical Remazol Black exhausted dyebath liquor simulated, which was then treated with homogeneous [ozonation with hydroxy ions, and Fe(II) or Fe(III) with hydrogen peroxide] and heterogeneous (titanium dioxide with UV‐A irradiation) advanced oxidation processes. Treatment performance of the investigated advanced oxidation systems was comparatively assessed in terms of the environmental sum parameters total organic carbon, biochemical oxygen demand and spectrophotometric measurements. The results obtained clearly reveal that the investigated advanced oxidation processes are capable of completely decolourising and partially mineralising the dye solution and its simulated dyebath effluent under predetermined reaction conditions. During the application of alkaline ozonation at an ozone dose of 2340 mg/ml, a three‐fold biodegradability enhancement was observed.

Two commercial reactive dyes, the azo dye Reactive Black 5 and the copper phythalocyanine dye Reactive Blue 21, have been treated at a concentration of 75 mg l(-1) by titanium dioxide mediated photocatalytic (TiO2/UV), dark and UV-light assisted Fenton (Fe2+/H2O2) and Fenton-like (Fe3+/H2O2) processes in acidic medium. For the treatment of Reactive Black 5, all investigated advanced oxidation processes were quite effective in terms of colour, COD as well as TOC removal. Moreover, the relative growth inhibition of the azo dye towards the marine algae Dunaliella tertiolecta that was initially 70%, did not exhibit an increase during the studied advanced oxidation reactions and complete detoxification at the end of the treatment period could be achieved for all investigated treatment processes. However, for Reactive Blue 21, abatement in COD and UV-VIS absorbance values was mainly due to the adsorption of the dye on the photocatalyst surface and/or the coagulative effect of Fe3+/Fe2+ ions. Although only a limited fraction of the copper phythalocyanine dye underwent oxidative degradation, 47% of the total copper in the dye was already released after 1 h photocatalytic treatment.

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