A differential pulse stripping method for the simultaneous determination of lead and tin is proposed. The

procedure involves accumulation with dissolving of lead and tin on a hanging mercury drop electrode

(HMDE), followed by oxidation of dissolve lead and tin by voltammetric scan using differential pulse

modulation. The optimum experimental conditions are: 0.2 mol L1 HNO3, accumulation potential of

900 mV versus Ag/AgCl, accumulation time of 200 s, scan rate of 20 mV s1 and pulse height of

80 mV. Lead and tin peak currents were observed in the same potential region at about 400 mV. The

simultaneous determination of lead and tin by using voltammetry is a difficult problem in analytical

chemistry, due to voltammogram interferences. The resolution of mixture of lead and tin by the application

of least-squares support vector machines (LS-SVM)