Improved signals ratio resolution method by optimization of resolution function-simultaneous determination of Cu(II) and Cd(II) in water samples

Citation
Z. Grabaric et al., Improved signals ratio resolution method by optimization of resolution function-simultaneous determination of Cu(II) and Cd(II) in water samples, J AOAC INT, 82(5), 1999, pp. 1185-1196
Citations number
45
Categorie Soggetti
Agricultural Chemistry
Journal title
JOURNAL OF AOAC INTERNATIONAL
ISSN journal
10603271 → ACNP
Volume
82
Issue
5
Year of publication
1999
Pages
1185 - 1196
Database
ISI
SICI code
1060-3271(199909/10)82:5<1185:ISRRMB>2.0.ZU;2-A
Abstract
From an ecological and economical point of view, it is important to design analytical procedures for monitoring heavy metals in the environment and in dustrial processes in a way to minimize the use of hazardous reagents and r educe the analysis time. In this paper, a well-known dithizonate extraction -based method for the determination of many metal ions was improved by usin g chemometrical selectivity of the strongly overlapped spectra of copper an d cadmium dithizonates in CCl4 for their simultaneous determination from a single extraction at pH 10. The individual absorption spectra, having absor ption maxima difference of only 20 nm, were separated, and the metal ions w ere quantified by using an improved procedure for optimizing the resolving function in a recently proposed signals ratio method. The procedure consist s of using many different resolving functions and plotting the difference o f the mean of absolute and nonabsolute mean values of pseudosignals [PDMMV (PS)] against analyte concentrations obtained with each of the resolving fu nctions, thus obtaining 2 straight lines having intersections that give a u nique and reliable value of the unknown concentration of the individual ana lyte in mixture giving strongly overlapped spectra, In this way, the main d rawback of the signals ratio resolution method, that is, the visual estimat ion of optimal resolving function, is eliminated. The proposed parameter, P DMMV (PS), was tested by using both simulated and experimental spectra. Cop per was determined in the mixture with ca 20-fold excess of cadmium, and ca dmium was determined in ca 10-fold excess of copper at submicromolar concen tration levels.