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In present study, efficiency of three rapid, simple, and reliable sample preparation methods namely dispersive liquid–liquid microextraction (DLLME), air-assisted liquid–liquid microextraction (AALLME), and CO2-assisted liquid–liquid microextraction (CO2-ALLME) have been compared for the extraction and preconcentration of Pt(IV) and Pd(II) ions in environmental water samples prior to flame atomic absorption spectrometry. In this regard, the effect of various experimental parameters on efficiency of the methods like nature and amount of the disperser and extraction solvents, ionic strength, temperature, pH, etc., are investigated to reach high enrichment factors. Due to organic solvent consumption at µL level, all of the studied methods are inexpensive and convenient. The linear ranges of the calibration curves were 10.0–200, 6.0–175, and 6.0–175 μg L−1 for Pd(II), and 20–200, 4.0–200, and 7.0–200 μg L−1 for Pt (IV) ions in DLLME, AALLME, and CO2-ALLME methods, respectively. Extraction recoveries of 81.4, 92.1, and 88.9% for Pd (II) and 85.3, 98.4, and 93.4% for Pt(IV) ions were obtained in DLLME, AALLME, and CO2-ALLME, respectively. Finally, the developed methods were successfully used for the analysis of Pt(IV) and Pd(II) in various water samples. [ABSTRACT FROM AUTHOR]

A green, simple, rapid, and efficient ligandless air-assisted liquid-liquid microextraction procedure based on solidification of a ternary deep eutectic solvent was developed for the extraction of trace amounts of cadmium(II) and zinc(II) ions in aqueous samples prior to their determination by flame atomic absorption spectrometry. For this purpose, the deep eutectic solvent is formed by mixing sorbitol, menthol, and mandelic acid at a suitable mole ratio and after heating for a short time, a deep eutectic solvent with low density compared to water is synthesised. The synthesised solvent is used as a chelating agent and also as an extraction solvent. Under the optimum experimental conditions, the linear ranges were obtained in the ranges of 0.5–12.5 and 0.5–10.0 µg L−1 for Zn(II) and Cd(II), respectively. The relative standard deviations (n = 6, C = 2.5 µg L−1 of each cation) were 4.2% and 3.4%, for Cd(II) and Zn(II), respectively. Moreover, the obtained detection limits were 0.15 and 0.12 µg L−1 for Cd(II) and Zn(II), respectively. The accuracy of the developed method was studied by analysing SPS-WW2 Batch 108 water as a certified reference material. Finally, the proposed method was successfully applied in the determination of Cd(II) and Zn(II) ions in water and fruit juice samples. Abbreviations: AALLME: Air-assisted liquid-liquid microextraction; ER: Extraction recovery; FAAS: Flame atomic absorption spectrometry; LOD: Limit of detection; LOQ: Limit of quantification; RSD: Relative standard deviation [ABSTRACT FROM AUTHOR]

A green, simple, rapid and efficient solventless temperature-assisted homogeneous liquid-liquid microextraction based on 8-hydroxyquinoline as complexing agent and extractant, followed by flame atomic absorption spectrometry was developed for the extraction, enrichment, and determination of trace amounts of nickel and cobalt in aqueous samples. For this purpose, first, a specified amount of 8-hydroxyquinoline is added to the analytes solution. Then the temperature of the solution is increased to melt 8-hydroxyquinoline and form a homogeneous solution. Then, it is cooled to room temperature and a cloudy solution is formed due to decreasing 8-hydroxyquinoline solubility. The solution is then centrifuged, and 8-hydroxyquinoline particles containing the produced complexes (8-hydroxyquinoline-cation) are collected at the bottom of the tube. They are removed and dissolved in a suitable solvent and injected to the detection system. The main parameters affecting the extraction efficiency, such as the amount of 8-hydroxyquinoline, solvent nature, pH, extraction temperature and heating time were investigated. Under optimum conditions, linear ranges for Co(II) and Ni(II) were 1-100 and 0.5-75 µg L−1, respectively. Relative standard deviations for intra- and inter-day precisions calculated from six repeated determinations at three different concentrations of Co(II) and Ni(II) were ≤5.2 %. Moreover, the obtained detection limits of the analytes were 0.35 and 0.20 µg L−1 for Co(II) and Ni(II), respectively. The accuracy of the developed procedure was checked by analysing SPS-WW2 Batch 108 water as a certified reference material. Finally, the developed method was successfully applied for the determination of the selected cations in water and fruit juice samples. [ABSTRACT FROM AUTHOR]