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The present paper presents the study of the decolorisation of real textile effluent by constant current electrolysis in a flow-cell using a Ti/Ru(0.3)Ti(0.7)O(2) DSA type electrode. The effect of increasing the chloride ion concentration on the efficiency of colour removal is discussed. Attempts to perform galvanostatic oxidation (40 and 60 mA cm(-2)) on the as-received effluent demonstrate that colour removal and total organic carbon (TOC) removal are limited. If the conductivity of the effluent is increased by adding 0.033 mol L(-1) Na(2)SO(4), little increase in the extent of colour/TOC removal is observed. However, when Na(2)SO(4) is substituted, stepwise, with NaCl (while maintaining the ionic strength constant) appreciable colour/TOC removal is observed. The study of the effect of increasing the current density demonstrates that total colour removal is possible at high currents. The efficiencies of colour and TOC removal are discussed in terms of the Energy per order (E(EO)/kWh m(-3)order(-1)) and Energy consumption (E(C)/kWh kg(-1)TOC), respectively. Finally, the extent of colour removal is compared to consent levels presented in the literature.

This paper presents the study of a prospective electrochemical treatment system for the pesticide carbaryl. Three different dimensionally stable anodes were employed (Ti/Ru0.3 Ti0.7 O2, Ti/Ru0.3 Sn0.7 O2 and Ti/Ir0.3 Ti0.7 O2) and the effect of current density (10, 20, 40 and 60 mA cm(-2)) and supporting electrolyte (0.1 mol L(-1) NaCl and 0.033 mol L(-1) H2SO4) is discussed. All the electrodes present a low level of carbaryl and total organic carbon removal in H2SO4, even at highly positive potentials, indicating that the application of current is not, in itself, sufficient to promote effective oxidation of the pesticide and its products. However, in the presence of NaCl all the electrodes used present rapid diminishing of the carbaryl and total organic carbon content, thus suggesting enhanced activity. The results demonstrate the participation of partially oxidised Cl- species at the electrode surface, which act as an intermediate in the electron transfer between the pesticide molecule and the electrode. Thus, under such conditions, the feasibility of the electrochemical route for the treatment (total or partial) of waste that contains carbaryl is evident.