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Solidified floating organic drop microextraction for speciation of selenium and its distribution in selenium-rich tea leaves and tea infusion by electrothermal vapourisation inductively coupled plasma mass spectrometry

机译:电热汽化电感耦合等离子体质谱法测定凝固的漂浮有机液滴微萃取对硒的形成及其在富硒茶叶中的分布和茶的浸入

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Solidified floating organic drop microextraction was combined with electrothermal vapourisation inductively coupled plasma mass spectrometry for Se species in Se-rich tea leaves and tea infusion, including total, suspended, soluble, organic and inorganic Se as well as Se(IV) and Se(VI). Ammonium pyrrolidinedithiocarbamate was used as both chelating reagent and chemical modifier in this study. Se(IV) and Se(VI) were separated at pH range of 2.0-5.0. An enrichment factor of 500 was obtained for Se(IV) from this method. Under the optimum conditions, the detection limits for Se(IV) and Se(VI) were 0.19 and 0.26 pg mL(-1), respectively. The relative standard deviations were less than 5.5% (c=0.1 ng mL(-1), n = 9). This method was applied for Se species, its content and distribution in Se-rich tea leaves and tea infusion with satisfactory results. The recoveries of spike experiments are in the range of 92.2-106%. A certified reference material of tea leaves was analyzed by this method, and the results were in agreement with certified values. (C) 2014 Elsevier Ltd. All rights reserved.
机译:固化的漂浮有机液滴微萃取与电热汽化电感耦合等离子体质谱法结合用于富硒茶叶中的硒物种和茶的浸入,包括总,悬浮,可溶性,有机和无机硒以及硒(IV)和硒(VI) )。吡咯烷二硫代氨基甲酸铵在本研究中既用作螯合剂,又用作化学改性剂。在2.0-5.0的pH范围内分离出Se(IV)和Se(VI)。通过这种方法获得的Se(IV)富集系数为500。在最佳条件下,Se(IV)和Se(VI)的检出限分别为0.19和0.26 pg mL(-1)。相对标准偏差小于5.5%(c = 0.1 ng mL(-1),n = 9)。该方法用于富硒茶叶和茶浸液中硒的种类,含量和分布,效果令人满意。加标实验的回收率在92.2-106%之间。通过该方法分析了茶叶的认证参考物质,其结果与认证值相符。 (C)2014 Elsevier Ltd.保留所有权利。

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