6533b838fe1ef96bd12a4ef8

RESEARCH PRODUCT

Analyser of chromium and/or cobalt

Pilar Campíns-falcóFrancisco Bosch-reigLuis Antonio Tortajada-genaro

subject

Detection limitAnalyserAnalytical chemistrychemistry.chemical_elementBiochemistryAnalytical ChemistryChemometricsChromiumCertified reference materialschemistryStandard additionPartial least squares regressionEnvironmental ChemistryCobaltSpectroscopy

description

Abstract Two stopped-flow manifolds have been proposed for individual or simultaneous determination of chromium and cobalt in water samples. Automated procedures based on multicommutation systems have emphasised the differences of their catalytic effect in luminol–hydrogen peroxide chemiluminescence reaction. A more rapid decay of signal was observed for Co for both configurations (flow injection or continuous injection). The influence of chemical and hydrodynamic variables has been studied in order to establish the robustness of method. The analysis rate was lower 1.5 min per replicate. Chemometric tools have been employed for the resolution of their contributions. Partial least squares (PLS) and H-point standard additions method (HPSAM) were used as multivariate calibration models. The percentages of explained variance were 97–99% (two factors). PLS and HPSAM obtained similar results. HPSAM provided a simple calibration model contributing to develop an analyser for chromium and/or cobalt. Standard mixtures, spiked samples and a certified reference material validated the proposed strategy. The applicability has been demonstrated by the determination of Cr and Co concentration in different water samples. The best results have been obtained for continuous injection providing more robust predictions. The achieved detection limit was 0.2 μg/l for both metals.

https://doi.org/10.1016/s0003-2670(03)00677-9