The silver electrode in square-wave anodic stripping voltammetry. Determination of Pb2+ without removal of oxygen

被引:96
作者
Brand, M [1 ]
Eshkenazi, I [1 ]
KirovaEisner, E [1 ]
机构
[1] TEL AVIV UNIV,RAYMOND & BEVERLY SACKLER FAC EXACT SCI,SCH CHEM,IL-69978 TEL AVIV,ISRAEL
关键词
D O I
10.1021/ac970420f
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A silver rotating disk electrode is used for the determination of lead in concentrations from 2 x 10(-9) to 3 x 10(-7) M by square-wave anodic stripping voltammetry (SWASV) without removal of oxygen. The repeatability of consecutive SWASV runs in synthetic solutions covering the entire concentration range is better than 2%. The calibration curve is represented by a correlation coefficient of at least 0.999. The detection limit for a 2-min electrodeposition is 0.5 nM. Up to 600 runs can be carried out on synthetic solutions without any pretreatment of the electrode. A 4-fold excess of Cd2+ and a 10 000-fold excess of Cu2+ do not interfere with the determination of part-per-billion concentrations of Pb2+. Surfactants present in tap water distort the SWASV. Improvement of the analytical response in tap water is achieved by pretreatment of the samples: irradiation at 254 nm or digestion with HNO3. During anodic stripping voltammetry in the concentration range studied, a uniformly distributed submonolayer of lead, occupying 0.02%-1% of the real surface of the electrode, is formed by underpotential deposition, Linearity in calibration plot is achieved up to 1% electrode coverage; in terms of the experimental parameters of the deposition step (rate of rotation and time of electrolysis), this condition for linearity is C(Pb2+)N(1/2)t(d) less than or equal to 2.2 x 10(5) nM rpm(1/2)s.
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页码:4660 / 4664
页数:5
相关论文
共 12 条
[1]   IN-LINE ULTRAVIOLET-DIGESTION OF NATURAL-WATER SAMPLES FOR TRACE-METAL DETERMINATION USING AN AUTOMATED VOLTAMMETRIC SYSTEM [J].
ACHTERBERG, EP ;
VAN DEN BERG, CMG .
ANALYTICA CHIMICA ACTA, 1994, 291 (03) :213-232
[2]   FORMATION OF METAL LAYERS [J].
ASTLEY, DJ ;
HARRISON, JA ;
THIRSK, HR .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1968, 19 (04) :325-&
[3]   ADSORPTIVE STRIPPING VOLTAMMETRY ON MERCURY FILM ELECTRODES IN THE PRESENCE OF SURFACTANTS [J].
ECONOMOU, A ;
FIELDEN, PR .
ANALYST, 1993, 118 (11) :1399-1404
[4]   Cathodic stripping voltammetry of selenium(IV) at a silver disk electrode [J].
Ishiyama, T ;
Tanaka, T .
ANALYTICAL CHEMISTRY, 1996, 68 (21) :3789-3792
[5]  
KOLB DM, 1974, J ELECTROANAL CHEM, V54, P25, DOI 10.1016/0368-1874(74)85093-8
[6]  
KOLB DM, 1978, ADV ELECTROCHEMISTRY, V11
[7]   USE OF SILICA FOR ADSORPTIVE STRIPPING VOLTAMMETRY IN THE PRESENCE OF ORGANIC SURFACTANTS [J].
KUBIAK, W ;
WANG, J .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1989, 258 (01) :41-48
[8]   ANODIC-STRIPPING VOLTAMMETRY OF LEAD WITH MICROLITER VOLUMES OF ELECTROLYTES AND SILVER-PLATED GLASSY-CARBON ELECTRODES [J].
MIWA, T ;
NISHIMURA, Y ;
MIZUIKE, A .
ANALYTICA CHIMICA ACTA, 1982, 140 (01) :59-64
[9]   STRUCTURAL ASPECTS OF ELECTROCHEMICAL ADSORPTION ON QUASI-PERFECT SILVER AND CADMIUM ELECTRODES [J].
POPOV, A .
ELECTROCHIMICA ACTA, 1995, 40 (05) :551-559
[10]   THE ELECTRODEPOSITION BEHAVIOR OF A SIMPLE ION [J].
ROGERS, LB ;
STEHNEY, AF .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1949, 95 (02) :25-32