Answers are grounded in this paper and cite their sources.
A single-valve sequential injection setup is suggested for automation of an air-assisted liquid-phase microextraction. In order to eliminate parasitic signals, the stopped flow detection mode was employed. The aqueous phase (1.5 mL), containing chromium(VI), chloride ions (0.6 mol L−1), sulphuric acid (0.07 mol L−1) and dimethyl indocarbocyanine dye (1.33 × 10−4 mol L−1), was dispensed into the extraction chamber and was followed by moderate injection of a 250 μL organic phase and intense mixing by multiple air bubbling. The extraction phase was then submitted for stopped flow UV-Vis spectrophotometric detection at 560 nm wavelength. The calibration plot was linear up to 104 μg L−1 of chromium(VI). The limit of detection, calculated as 3s of a blank test (n = 10), was found to be 4.5 μg L−1. The developed procedure was applied for the determination of Cr(VI) in various water samples.
No takes yet. Share an insight, caveat, or question.
Alexovič et al. (2013) studied this question.
Synapse has enriched 5 related papers. Consider them for comparative context: