Anodic Stripping Voltammetry and Differential Pulse Polarography

2015 ◽  
pp. 133-148
Author(s):  
Jimmy J. Street ◽  
William M. Peterson
Keyword(s):  
Anodic Stripping Voltammetry ◽  
Stripping Voltammetry ◽  
Differential Pulse ◽  
Differential Pulse Polarography ◽  
Pulse Polarography ◽  
Anodic Stripping

Determination of Copper, Nickel, and Chromium in Foods

1983 ◽  
Vol 66 (3) ◽  
pp. 620-624
Author(s):  
Walter Holak
Keyword(s):  
Anodic Stripping Voltammetry ◽  
Stripping Voltammetry ◽  
Differential Pulse ◽  
Atomic Absorption Spectrophotometry ◽  
Differential Pulse Polarography ◽  
National Bureau ◽  
Pulse Polarography ◽  
Digestion Technique ◽  
Determination Of Copper

Abstract A collaboratively studied method for Pb, Cd, As, Se, and Zn that uses a closed system digestion technique has now been extended to include 3 additional elements, Cu, Ni, and Cr. Cu is determined by either atomic absorption spectrophotometry or anodic stripping voltammetry, depending on the concentration. Ni and Cr are determined by differential pulse polarography. Analysis of National Bureau of Standards reference materials by this procedure gives values in close agreement with the accepted values. Recoveries from applesauce and chicken spiked at 0.6-4 μg/g are in the 92-101% range. The sensitivity of the multielement procedure is 0.34,0.14, and 0.24 μg/g for Cu, Ni, Cr, respectively, at the 90% confidence level.

Methylmercury Generation in Seawater by Transmethylation Reactions of Organolead and Organotin Compounds With Inorganic Mercury as Monitored by Multinuclear Magnetic-Resonance and Electrochemical Techniques

1986 ◽  
Vol 39 (8) ◽  
pp. 1167 ◽  
Author(s):  
GN Howell ◽  
MJ Oconnor ◽  
AM Bond ◽  
HA Hudson ◽  
PJ Hanna ◽  
...  
Keyword(s):  
Magnetic Resonance ◽  
Anodic Stripping Voltammetry ◽  
Electrochemical Techniques ◽  
Inorganic Mercury ◽  
Stripping Voltammetry ◽  
Differential Pulse ◽  
Differential Pulse Polarography ◽  
Resonance Spectroscopy ◽  
Ambient Temperatures ◽  
Pulse Polarography

The generation of methylmercury species by reactions between inorganic mercury and methylated forms of lead and tin in seawater and other matrices is described. The reactions were investigated by 119Sn, 199Hg and 207Pb multinuclear Fourier transform magnetic resonance spectroscopy and by differential pulse polarography and anodic stripping voltammetry. Methylmercury chloride is shown to be produced from mixtures of inorganic mercury with methyltin or methyllead species over the 10-2-10-8 M concentration range at ambient temperatures in seawater and artificial seawater.

Polarographic and Voltammetric Determination of Trace Amounts of 3-Nitrofluoranthene

2006 ◽  
Vol 71 (11-12) ◽  
pp. 1571-1587 ◽  
Author(s):  
Karel Čížek ◽  
Jiří Barek ◽  
Jiří Zima
Keyword(s):  
River Water ◽  
Solid Phase ◽  
Mercury Electrode ◽  
Stripping Voltammetry ◽  
Differential Pulse ◽  
Differential Pulse Polarography ◽  
Pulse Polarography ◽  
Dropping Mercury Electrode ◽  
Separation And Preconcentration

The polarographic behavior of 3-nitrofluoranthene was investigated by DC tast polarography (DCTP) and differential pulse polarography (DPP), both at a dropping mercury electrode, differential pulse voltammetry (DPV) and adsorptive stripping voltammetry (AdSV), both at a hanging mercury drop electrode. Optimum conditions have been found for its determination by the given methods in the concentration ranges of 1 × 10-6-1 × 10-4 mol l-1 (DCTP), 1 × 10-7-1 × 10-4 mol l-1 (DPP), 1 × 10-8-1 × 10-6 mol l-1 (DPV) and 1 × 10-9-1 × 10-7 mol l-1 (AdSV), respectively. Practical applicability of these techniques was demonstrated on the determination of 3-nitrofluoranthene in drinking and river water after its preliminary separation and preconcentration using liquid-liquid and solid phase extraction with the limits of determination 4 × 10-10 mol l-1 (drinking water) and 2 × 10-9 mol l-1 (river water).

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