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Abstract The corrodibility of the commercial Pb-1.7%Sb alloy in sulphuric acid solutions in the absence and presence of phosphoric acid under open circuit and potentiostatic and galvanostatic polarization conditions were studied by potential, cyclic voltammetry and electrochemical impedance spectroscopy. Addition of H3PO4 increase the corrodibility of the alloy by retardation of the growth of the passive PbSO 4 film that in turn slowdown the corrosion rate. The efficiency of PbO2 formation and the self-discharge of PbO 2 decreases with increasing oxidation current. The presence of H 3PO4 leads to a substantial decrease in both the efficiency of PbO 2 formation and consequently its self-discharge. Life cycle tests show that H 3PO4 causes lesser surface penetration as a result of inhibition of PbSO 4 via formation of PbHPO 4 and adsorption of phosphate on PbSO 4 . |