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

被引:11
作者
PIRZAD, R
MOREIRA, JC
RANGEL, AOSS
ALONSO, RM
EDMONDS, TE
FOGG, AG
机构
关键词
CATHODIC STRIPPING VOLTAMMETRY; HANGING MERCURY DROP ELECTRODE; POLY-L-LYSINE; MODIFIED ELECTRODE; NITROPRUSSIDE; COPPER(II);
D O I
10.1039/an9941900963
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The nitroprusside anion, Fe(CN)(5)NO2-, can be accumulated from pH 5 Britton-Robinson buffer solution on to the surface of a hanging mercury drop electrode (HMDE), which has been modified by means of adsorbed poly-L-lysine and which is held on open circuit. This was shown by closing the circuit at -0.2 V versus the Ag-AgCI electrode, after accumulation, and scanning cathodically by use of differential-pulse voltammetry. The voltammetric peak that was observed at about -0.6 V, however, was that for the adsorbed product of the first reduction step of nitroprusside, reported to be Fe(CN)(4)NO2-, which is the product of the one-electron reduction of the nitroprusside ion [to Fe(CN)(5)NO3-] followed by the elimination of CN-. When accumulation Was carried out at the peak potential of the first polarographic reduction peak of nitroprusside (-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 dm(-3) hydrochloric acid) solution, nitroprusside can be accumulated very efficiently between 0 and -0.1 V at an unmodified HMDE in the presence of excess of copper(II). The cathodic stripping peak at about -0.35 V is due to the reduction of an adsorbed copper/reduced nitroprusside species, which has not been fully identified, but is most probably either the copper(I) or copper(II) salt of Fe(CN)(4)NO2-. This signal was enhanced slightly when accumulation was effected at a poly-L-lysinemodified HMDE. Linear calibration graphs were obtained for up to at least 1 x 10(-7) mol dm(-3) for the determination of nitroprusside at both pH 5 and pH 2, by using cathodic stripping voltammetric methods based on the above electrode processes, and the limit of detection was calculated to be about 5 x 10(-10) mol dm(-3) in both instances. Relative standard deviations were typically <2% at the 1 x 10(-8) mol dm(-3) level.
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页码:963 / 968
页数:6
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