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

被引:5
作者
Wang, Chin-Yi [1 ]
Chang, Da-An [1 ]
Shen, Yuzhou [1 ]
Sun, Yuh-Chang [1 ]
Wu, Chien-Hou [1 ]
机构
[1] Natl Tsing Hua Univ, Coll Nucl Sci, Dept Biomed Engn & Environm Sci, Hsinchu 30013, Taiwan
关键词
crown ethers; ion chromatography; strontium; vortex-assisted liquid-liquid microextraction; ATOMIC-EMISSION-SPECTROMETRY; CATION-EXCHANGE COLUMN; ION CHROMATOGRAPHY; CROWN-ETHER; SOLVENT-EXTRACTION; SR RESIN; CAPILLARY-ELECTROPHORESIS; SELECTIVE SEPARATION; BISPHENOL-A; SEA-WATER;
D O I
10.1002/jssc.201700205
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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 mu L 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.
引用
收藏
页码:3866 / 3872
页数:7
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