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首页> 外文期刊>Spectrochimica acta, Part A. Molecular and biomolecular spectroscopy >Indirect spectrophotometric determination of ultra trace amounts of selenium based on dispersive liquid-liquid microextraction-solidified floating organic drop
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Indirect spectrophotometric determination of ultra trace amounts of selenium based on dispersive liquid-liquid microextraction-solidified floating organic drop

机译:分散液-液微萃取-凝固的悬浮有机液滴间接分光光度法测定超痕量硒

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摘要

(Figure Presented) A novel dispersive liquid-liquid microextraction- solidified floating organic drop (DLLME-SFOD) method combined with fiber optic-linear array detection spectrophotometry has been developed for the indirect determination of selenium. The method is based on the oxidation of the I- to iodine by inorganic Se(IV). The produced I_2 reacts with the excess of I- ions in acidic media to give triiodide ions. The I_3 - is then extracted into 1-undecanol by DLLME-SFOD upon the formation of an ion pair with cetyltrimethylammonium cation. The extracted ion pair is determined by measuring its absorption at 360 nm. The absorbance signal is proportional to the selenium concentration in the aqueous phase. Under optimum conditions, the method provided an enrichment factor of 250 with a detection limit of 16.0 μg L~(-1) and a linear dynamic range of 40.0-1000.0 μg L~(-1). The relative standard deviation was found to be 2.1% (n = 7) at 100.0 μg L~(-1) concentration level. The method was successfully applied to the determination of selenium in water samples and selenium plus tablet.
机译:(显示的图)已经开发了一种新颖的分散液-液微萃取-凝固的漂浮有机液滴(DLLME-SFOD)方法与光纤线性阵列检测光度法相结合,用于间接测定硒。该方法基于无机Se(IV)将I-氧化为碘。产生的I_2与酸性介质中过量的I-离子反应生成三碘化物离子。然后,在与十六烷基三甲基铵阳离子形成离子对之后,通过DLLME-SFOD将I3-萃取至1-十一烷醇中。提取的离子对通过测量其在360 nm处的吸收来确定。吸光度信号与水相中的硒浓度成正比。在最佳条件下,该方法提供的富集因子为250,检测极限为16.0μgL〜(-1),线性动态范围为40.0-1000.0μgL〜(-1)。在100.0μgL〜(-1)浓度水平下,相对标准偏差为2.1%(n = 7)。该方法已成功地用于水样和硒加片中硒的测定。

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