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使用4',4″(5″)-二-(叔丁基环己基)-18-冠-6和四苯硼酸盐从水样中涡旋辅助液-液微萃取锶

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

作者信息

Wang Chin-Yi, Chang Da-An, Shen Yuzhou, Sun Yuh-Chang, Wu Chien-Hou

机构信息

Department of Biomedical Engineering and Environmental Sciences, College of Nuclear Science, National Tsing Hua University, Hsinchu, Taiwan.

出版信息

J Sep Sci. 2017 Oct;40(19):3866-3872. doi: 10.1002/jssc.201700205. Epub 2017 Aug 28.

Abstract

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.

摘要

建立了一种涡旋辅助液液微萃取方法,用于色谱测定水样中的锶。在该方法中,锶在四苯基硼酸盐作为抗衡阴离子的存在下与4',4″(5″)-二-(叔丁基环己基)-18-冠-6络合,这增加了离子缔合络合物的疏水性,从而提高了其向1-辛醇中的萃取效率。有机相中的锶用硝酸反萃回到水溶液中,然后通过离子色谱法进行测定。最佳微萃取条件如下:2.0 mL水样,加入3 mM四苯基硼酸盐;150 μL 1-辛醇作为萃取相,加入10 mM DtBuCH18C6;涡旋萃取时间为10 s;以6000 rpm离心4 min;用0.1 M硝酸反萃。在最佳条件下,锶的检测限为0.005 mg/L。校准曲线在0.01至2.5 mg/L范围内呈现良好的线性。本方法的日内和日间精密度令人满意,相对标准偏差分别为1.7%和2.1%。

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