Online coupling of fully automatic in-syringe dispersive liquid-liquid microextraction with oxidative back-extraction to inductively coupled plasma spectrometry for sample clean-up in elemental analysis: A proof of concept

A proof of concept of a novel automatic sample cleanup approach for metal assays in troublesome matrixes as a front-end sample pre-treatment to inductively coupled plasma optical emission spectroscopy – ICP-OES – is herein presented. Target metals, namely, copper, lead, and cadmium were complexed in...

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Veröffentlicht in:Talanta (Oxford) 2017-10, Vol.173, p.79-87
Hauptverfasser: Horstkotte, Burkhard, Fikarová, Kateřina, Cocovi-Solberg, David J., Sklenářová, Hana, Solich, Petr, Miró, Manuel
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Sprache:eng
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Zusammenfassung:A proof of concept of a novel automatic sample cleanup approach for metal assays in troublesome matrixes as a front-end sample pre-treatment to inductively coupled plasma optical emission spectroscopy – ICP-OES – is herein presented. Target metals, namely, copper, lead, and cadmium were complexed in-system quantitatively using ammonium pyrrolidine dithiocarbamate (APDC) and transferred into a minute volume of toluene as extractant employing lab-in-syringe magnetic stirring-assisted dispersive liquid-liquid microextraction (LIS-MSA-DLLME). After discharge of the sample, the analytes were back-extracted into nitric acid and injected on-line into ICP-OES. To promote and expedite this process in-syringe, advantage was taken from oxidative decomposition of the chelate by potassium iodate, reported in this article for the first time. Experimental conditions for LIS-MSA-DLLME were optimized by Box-Benkhen multivariate analysis using the geometric mean of analyte recoveries as the desirability function. Times of extraction and back-extraction of 300s and 100s, respectively, pH 5.5 at 30mmol/L acetate, 300µL of extraction solvent, and 600µmol/L of APDC were finally applied. Online interfacing to ICP-OES for back-extract analysis yielded average repeatabilities for Cd, Cu, and Pb of 2.9%, 3.5%, and 3.5% with limits of detections (3s) of 1.9, 1.4, and 5.6ng/mL, respectively. Oxidative back-extraction was proven reliable for the determination of metal species in coastal seawater, surrogate digestive fluids and soil leachates with recovery values for Cd, Cu, and Pb ranging from 90% to 118%, 68% to 104%, and 86% to 112%, respectively. [Display omitted] •In-syringe automation of dispersive liquid-liquid microextraction-backextraction.•First time use for automated extraction of metal chelates for elemental analysis.•Oxidative decomposition of chelates as a novel approach for metal release.•Online coupling to inductively coupled plasma-optical emission spectrometry.•Miniaturization of sample cleanup of digestive fluids, seawater, and soil leachates.
ISSN:0039-9140
1873-3573
DOI:10.1016/j.talanta.2017.05.063