6533b86efe1ef96bd12cbccb

RESEARCH PRODUCT

Determination of chromium(III) and chromium(VI) in mineral water by bidirectional electrostacking and electrothermal atomic absorption spectrometry

M. Luisa CerveraYouzhao HeAgustín PastorMiguel De La Guardia

subject

Detection limitChemistryAnalytical chemistrychemistry.chemical_elementConductivityBiochemistryAnalytical Chemistrylaw.inventionChromiumCertified reference materialslawStandard additionCalibrationEnvironmental ChemistryAtomic absorption spectroscopyQuantitative analysis (chemistry)Spectroscopy

description

Abstract A feasibility investigation was carried out on the use of bidirectional electrostacking for simultaneous separation and pre-concentration of Cr(III) and Cr(VI) and their electrothermal atomic absorption spectrometry (ETAAS) determination. The bidirectional electrostacking manifold was improved, and the effects of sample tube cross-section and electrostacking time on the pre-concentration factor were investigated. Results indicate that the sample tube cross-section and electrostacking time are the main influence factors on the electrostacking pre-concentration, as well as the electric field strength and ionic mobility. The method developed was suitable for the simultaneous separation and pre-concentration of micro- or trace cations and anions in low conductivity sample solutions. The dynamic calibration range for both, Cr(III) and Cr(VI), was from 0.5 to 10 μg l −1 using 20 μl sample volume and ETAAS determination. Standard addition method was used for the pre-concentration of Cr(III) and Cr(VI) in electrostacking procedure. The amounts of 100 ng l −1 Cr(III) and Cr(VI) were added into one of twin samples, which were pre-concentrated in parallel, for the pre-concentration factor calculation. The limit of detection for Cr(III) and Cr(VI) was 6 and 5 ng l −1 , respectively, for three times standard deviation (S.D.) of blank values ( n =7) and 10 min electrostacking, providing pre-concentration factors of the order of 10 times. The method was applied to analyze a certified reference material of simulated fresh water, and results were coincident with its certified value.

https://doi.org/10.1016/s0003-2670(01)01296-x