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Speciation of trace metals in natural waters: The influence of an adsorbed layer of natural organic matter (NOM) on voltammetric behaviour of copper (CROSBI ID 133617)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Louis, Yoann ; Cmuk, Petra ; Omanović, Dario ; Garnier, Cédric ; Lenoble, Véronique ; Mounier, Stéphane ; Pižeta, Ivanka Speciation of trace metals in natural waters: The influence of an adsorbed layer of natural organic matter (NOM) on voltammetric behaviour of copper // Analytica chimica acta, 606 (2008), 1; 37-44. doi: 10.1016/j.aca.2007.11.011

Podaci o odgovornosti

Louis, Yoann ; Cmuk, Petra ; Omanović, Dario ; Garnier, Cédric ; Lenoble, Véronique ; Mounier, Stéphane ; Pižeta, Ivanka

engleski

Speciation of trace metals in natural waters: The influence of an adsorbed layer of natural organic matter (NOM) on voltammetric behaviour of copper

The influence of an adsorbed layer of the natural organic matter (NOM) on voltammetric behaviour of copper on a mercury drop electrode in natural water samples was studied. The adsorption of NOM strongly affects the differential pulse anodic stripping voltammogram (DPASV) of copper, leading to its distortion. Phase sensitive a.c. voltammetry confirmed that desorption of adsorbed NOM occurs in general at accumulation potentials more negative than -1.4 V. Accordingly, an application of negative potential (-1.6 V) for a very short time at the end of the accumulation time (1% of total accumulation time) to remove the adsorbed NOM was introduced in the measuring procedure. Using this protocol, a well resolved peak without interferences was obtained. It was shown that stripping chronopotentiogram of copper (SCP) in the depletive mode is influenced by the adsorbed layer in the same manner as DPASV. The influence of the adsorbed NOM on pseudopolarographic measurements of copper and on determination of copper complexing capacity (CuCC) was demonstrated. A shift of the peak potential and the change of the half-peak width on the accumulation potential (for pseudopolarography) and on copper concentration in solution (for CuCC) were observed. By applying a desorption step these effects vanished, yielding different final results.

anodic stripping voltammetry ; metal complexing capacity ; organic matter ; pseudopolarography ; speciation ; trace metals

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Podaci o izdanju

606 (1)

2008.

37-44

objavljeno

0003-2670

1873-4324

10.1016/j.aca.2007.11.011

Povezanost rada

Geologija, Kemija

Poveznice
Indeksiranost