首页> 外文期刊>International journal of environmental analytical chemistry >Magnetic dispersive solid phase extraction using modified magnetic multi-walled carbon nanotubes combined with electrothermal atomic absorption spectrometry for the determination of selenium
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Magnetic dispersive solid phase extraction using modified magnetic multi-walled carbon nanotubes combined with electrothermal atomic absorption spectrometry for the determination of selenium

机译:改进的磁性多壁碳纳米管与电热原子吸收光谱法结合用于磁性分散固相萃取测定硒

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摘要

A novel magnetic dispersive solid phase extraction method using magnetic multi-walled carbon nanotubes modified with 5-mercapto-3-phenyl-1,3,4-thiadiazole-2-thione potassium salt (bismuthiol II) (MMWCNTs@Bis) as the sorbent was developed for the separation and preconcentration of inorganic selenium (IV) prior to its determination by electrothermal atomic absorption spectrometry. The prepared MMWCNTs@Bis sorbent was characterised by Fourier transform infrared spectroscopy, scanning electron microscopy, vibrating sample magnetometer and X-ray diffraction. Total selenium was determined after reduction of Se(VI) to Se(IV) by addition of hydrochloric acid and heating the mixture in a boiling water bath. Se(VI) concentration was determined from the difference between the amounts of total selenium and Se(IV). Under the optimised experimental conditions, an enhancement factor of 196 and a detection limit (based on 3S(b)/m) of 0.003 mu gL(-1) was obtained for aqueous samples. The relative standard deviation at 0.1 mu gL(-1) concentration level of Se(IV) (n=6) was found to be 5.2 and 7.7% for intra- and inter-day analysis, respectively. The method was successfully applied to the determination of inorganic selenium species in water and total selenium in food samples.
机译:一种以5-巯基-3-苯基-1,3,4-噻二唑-2-硫酮钾盐(bismuthiol II)(MMWCNTs @ Bis)为吸附剂修饰的磁性多壁碳纳米管的新型磁性分散固相萃取方法用电热原子吸收光谱法测定无机硒(IV)之前,已开发出用于分离和预浓缩硒的方法。通过傅立叶变换红外光谱,扫描电子显微镜,振动样品磁力计和X射线衍射对所制备的MMWCNTs @ Bis吸附剂进行表征。通过添加盐酸并将混合物在沸水浴中加热,将硒(VI)还原为硒(IV)后,测定总硒。从总硒和Se(IV)量之间的差确定Se(VI)浓度。在优化的实验条件下,水性样品的增强因子为196,检出限(基于3S(b)/ m)为0.003μgL(-1)。在日内和日间分析中,Se(IV)(n = 6)的浓度为0.1μgL(-1)时的相对标准偏差分别为5.2和7.7%。该方法成功地用于食品中水和总硒中无机硒的测定。

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