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Arsenic speciation in natural waters by cathodic stripping voltammetry
Analytica Chimica Acta, 2010Contamination of groundwater with arsenic (As) is a major health risk through contamination of drinking and irrigation water supplies. In geochemically reducing conditions As is mostly present as As(III), its most toxic species. Various methods exist to determine As in water but these are not suitable for monitoring arsenic speciation at its original ...
Kristoff, Gibbon-Walsh +2 more
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Cathodic stripping voltammetry of the copper–1,10‐phenanthroline complex
Electroanalysis, 1995AbstractCathodic stripping voltammetry of copper, based on the accumulation and reduction of its complex with 1,10‐phenanthroline (phen), has been studied. The complex is reduced in two steps from CuI–phen and CuII–phen to copper amalgam at potentials of −0.43 and −0.62 V vs. Ag/AgCl, respectively.
Čuljak, Ivan +2 more
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Determination of mebendazole in urine by cathodic stripping voltammetry
Analytica Chimica Acta, 1996Abstract A cathodic stripping procedure has been developed for the determination of mebendazole. An 8 min accumulation time on a 0.1 M acetic acid/acetate pH = 5 buffer solution gives rise to a detection limit of 3 × 10−11M. An extraction with ether has been developed for the determination of mebendazole in urine. Concentrations of 5 × 10−9M in urine
A.J. Conesa, J.M. Pinilla, L. Hernández
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Analysis of arsenic(V) by cathodic stripping voltammetry
Analytica Chimica Acta, 1995Abstract A novel electrochemical stripping approach is presented for the trace measurement of arsenate. It is based on the reduction of As(V) in a mannitol and perchlorate containing solution, the coprecipitation with copper and the voltammetric determination by further reduction to AsH3 at the hanging mercury drop electrode.
U. Greulach, G. Henze
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Determination of selenium by catalytic cathodic stripping voltammetry
Analytica Chimica Acta, 2000A procedure is described for the determination of selenium in natural waters using cathodic stripping voltammetry in the presence of rhodium. Advantage is taken from a catalytic effect on the electrochemical reduction of protons in the presence of a mixed complex of selenide with rhodium and chloride, containing Cl‐Rh‐SeH species.
Britta Lange, Constant M.G. van den Berg
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Cathodic stripping voltammetry of glutathione in natural waters
The Analyst, 1993The electrochemistry of metal–glutathione complexes at a hanging mercury drop electrode was investigated and a procedure was optimized to determine glutathione in natural waters using cathodic stripping voltammetry (CSV). Adsorption of complexes of mercury(I) and copper(I) with glutathione can be utilized to preconcentrate the glutathione on the ...
Anne-Christine Le Gall +1 more
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Cathodic stripping voltammetry of Cu2Se at mercury electrodes
Journal of Electroanalytical Chemistry, 1994The electrochemistry of the codeposition of Se(IV) and Cu2+ at a hanging-mercury-drop electrode has been studied in detail in 0.1 M HClO4 or HCl solutions.
G. Mattsson, L. Nyholm, Å. Olin
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Square-wave adsorptive cathodic stripping voltammetry of pantoprazole
Journal of Pharmaceutical and Biomedical Analysis, 2003Adsorption and reduction of pantoprazole were investigated by cyclic and square-wave voltammetry on a hanging mercury drop electrode in Britton-Robinson buffers at pH 2.0-11.0. The reduction process gave rise to a single peak within the entire pH range.
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Determination of dimethoate in water by cathodic stripping square-wave voltammetry
Artículos en revistasThis article describes the direct-determination of the pesticide dimethoate In river water in an alkalin media and accumulaton medium through cathodic stripping voltammetry. By employing an alkaline potential of 30 mV, reduction peak
Galán Estella, Fernando +3 more
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Cathodic stripping voltammetry of catechol and some catecholamines
Journal of Electroanalytical Chemistry and Interfacial Electrochemistry, 1986Abstract The cathodic stripping voltammetry of catechol, L-dopa, dopamine and norepinephrine at a hanging mercury electrode is described. These compounds can be determined at concentrations of 2 × 10−8 to 5 × 10−7M. Interference by surface-active agents and other organic compounds was studied.
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