The oxygen reduction reaction (ORR) was studied on chalcosite, pyrite and g
alene by cyclic voltammetry and stationary potential measurements using a d
ouble channel electrode flow cell (DCEFC) at pH = 14. The electrode surface
was characterized using thermodynamic and voltammetric data. Stationary vo
ltammetry results show that molecular oxygen is reduced to peroxide ions, H
O2-, in all cases. At experimental pH, the O-2 reduction occurs on chalcosi
te surface containing Cu2S film and on pyrite surface supporting Fe(OH)(3)
film. In the case of galene, the formation of elemental S on generator elec
trode (due to surface chemical oxidation) and collector electrode of the fl
ow cell (due to oxidation of the generated sulphide ions) hinder the electr
oreduction of oxygen, impeding the determination of the kinetic parameters,
k(1) (direct way) and k(2) (indirect way). From the k(1)/k(2) ratio, chalc
osite appears to be the best catalyst for ORR. In fact, this mineral produc
es less HO2 ions than galene and the oxidation of flotation collectors is r
educed.