Vortex‐assisted liquid–liquid microextraction of strontium from water samples using 4′,4″(5″)‐di‐(tert‐butylcyclohexano)‐18‐crown‐6 and tetraphenylborate

A vortex‐assisted liquid–liquid microextraction method was developed for the chromatographic determination of strontium in aqueous samples. In the method, strontium was complexed with 4′,4″(5″)‐di‐(tert‐butylcyclohexano)‐18‐crown‐6 in the presence of tetraphenylborate as the counter anion, which inc...

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Veröffentlicht in:Journal of separation science 2017-10, Vol.40 (19), p.3866-3872
Hauptverfasser: Wang, Chin‐Yi, Chang, Da‐An, Shen, Yuzhou, Sun, Yuh‐Chang, Wu, Chien‐Hou
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container_end_page 3872
container_issue 19
container_start_page 3866
container_title Journal of separation science
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creator Wang, Chin‐Yi
Chang, Da‐An
Shen, Yuzhou
Sun, Yuh‐Chang
Wu, Chien‐Hou
description A vortex‐assisted liquid–liquid microextraction method was developed for the chromatographic determination of strontium in aqueous samples. In the method, strontium was complexed with 4′,4″(5″)‐di‐(tert‐butylcyclohexano)‐18‐crown‐6 in the presence of tetraphenylborate as the counter anion, which increased the hydrophobicity of the ion‐association complex, resulting in its improved extraction into 1‐octanol. Strontium from the organic phase was stripped with nitric acid back to aqueous solution and determined by ion chromatography. The optimum microextraction conditions were as follows: 2.0 mL aqueous samples with 3 mM tetraphenylborate; 150 μL of 1‐octanol as the extractant phase with 10 mM DtBuCH18C6; vortex extraction time for 10 s; centrifugation at 6000 rpm for 4 min; stripping by 0.1 M nitric acid. Under the optimum conditions, the detection limit for strontium was 0.005 mg/L. The calibration curves showed good linearity over the range between 0.01 and 2.5 mg/L. Intra‐ and interday precisions of the present method were satisfactory with relative standard deviations of 1.7 and 2.1%, respectively.
doi_str_mv 10.1002/jssc.201700205
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In the method, strontium was complexed with 4′,4″(5″)‐di‐(tert‐butylcyclohexano)‐18‐crown‐6 in the presence of tetraphenylborate as the counter anion, which increased the hydrophobicity of the ion‐association complex, resulting in its improved extraction into 1‐octanol. Strontium from the organic phase was stripped with nitric acid back to aqueous solution and determined by ion chromatography. The optimum microextraction conditions were as follows: 2.0 mL aqueous samples with 3 mM tetraphenylborate; 150 μL of 1‐octanol as the extractant phase with 10 mM DtBuCH18C6; vortex extraction time for 10 s; centrifugation at 6000 rpm for 4 min; stripping by 0.1 M nitric acid. Under the optimum conditions, the detection limit for strontium was 0.005 mg/L. The calibration curves showed good linearity over the range between 0.01 and 2.5 mg/L. 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subjects crown ethers
Extraction processes
Hydrophobicity
ion chromatography
Linearity
Liquid-liquid extraction
Nitric acid
Octanol
Strontium
vortex‐assisted liquid–liquid microextraction
Vortices
title Vortex‐assisted liquid–liquid microextraction of strontium from water samples using 4′,4″(5″)‐di‐(tert‐butylcyclohexano)‐18‐crown‐6 and tetraphenylborate
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