Ti/IrO2-Ta2O5 electrodes prepared by thermal decomposition of the resp
ective chlorides were successfully employed as oxygen evolving electro
des for electroflotation of waste water contaminated with dispersed pe
ptides and oils. Service lives and rates of dissolution of the Ti/IrO2
-Ta2O5 electrodes were measured by means of accelerated life tests, e.
g. electrolysis in 0.5 M H2SO4 at 25-degrees-C and j = 2 A cm-2. The s
teady-state rate of dissolution of the IrO2 active layer was reached a
fter 600-700 h (0.095 mug Irh-1 cm-2) which is 200-300 times lower tha
n the initial dissolution rate. The steady-state rate of dissolution o
f iridium was found to be proportional to the applied current density
(in the range 0.5-3 A cm-2). The oxygen overpotential increased slight
ly during electrolysis (59-82 mV for j = 0.1 A cm-2) and the increase
was higher for the lower content of iridium in an active surface layer
. The service life of Ti/IrO2 (65 mol%)-Ta2O5 (35 mol%) in industrial
conditions of electrochemical devices was estimated to be greater than
five years.