DIFFERENTIAL-PULSE CATHODIC STRIPPING VOLTAMMETRIC DETERMINATION OF SODIUM-NITROPRUSSIDE AT A HANGING MERCURY DROP ELECTRODE AIDED BY COPPER(II) AND POLY-L-LYSINE MODIFICATION

The nitroprusside anion, Fe(CN)(5)NO2-, can be accumulated from pH 5 B ritton-Robinson buffer solution on to the surface of a hanging mercury drop electrode (HMDE), which has been modified by means of adsorbed p oly-L-lysine and which is held on open circuit. This was shown by clos ing the circuit at -0.2 V versus the Ag-AgCI electrode, after accumula tion, and scanning cathodically by use of differential-pulse voltammet ry. The voltammetric peak that was observed at about -0.6 V, however, was that for the adsorbed product of the first reduction step of nitro prusside, reported to be Fe(CN)(4)NO2-, which is the product of the on e-electron reduction of the nitroprusside ion [to Fe(CN)(5)NO3-] follo wed by the elimination of CN-. When accumulation Was carried out at th e peak potential of the first polarographic reduction peak of nitropru sside (-0.35 V), the peak current at -0.6 V was enhanced 4-fold, which indicated that the Fe(CN)(NO2-)-N-4 was accumulated on poly-L-lysine more extensively than was the nitroprusside ion. From pH 2 (0.01 mol d m(-3) hydrochloric acid) solution, nitroprusside can be accumulated ve ry efficiently between 0 and -0.1 V at an unmodified HMDE in the prese nce of excess of copper(II). The cathodic stripping peak at about -0.3 5 V is due to the reduction of an adsorbed copper/reduced nitroprussid e species, which has not been fully identified, but is most probably e ither the copper(I) or copper(II) salt of Fe(CN)(4)NO2-. This signal w as enhanced slightly when accumulation was effected at a poly-L-lysine modified HMDE. Linear calibration graphs were obtained for up to at le ast 1 x 10(-7) mol dm(-3) for the determination of nitroprusside at bo th pH 5 and pH 2, by using cathodic stripping voltammetric methods bas ed on the above electrode processes, and the limit of detection was ca lculated to be about 5 x 10(-10) mol dm(-3) in both instances. Relativ e standard deviations were typically <2% at the 1 x 10(-8) mol dm(-3) level.