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使用4-溴-和4-氯-1,2-二氨基苯作为衍生试剂,通过气液色谱法测定生物材料中的硒。

Gas-liquid chromatographic determination of selenium in biological materials, using 4-bromo- and 4-chloro 1,2-diaminobenzene as derivatizing reagents.

作者信息

Bycroft B M, Clegg D E

出版信息

J Assoc Off Anal Chem. 1978 Jul;61(4):923-6.

PMID:681265
Abstract

A method is described for the gas-liquid chromatographic determination of traces of selenium in marine biological materials. The method is based on the reaction of Se(IV) with bromo- and chloro-substituted 1,2-diaminobenzenes. The benzoselenadiazoles so formed are sensitive to electron capture detection. The sample is digested in a nitric-perchloric acid mixture and selenium is reduced to the IV oxidation state. Different aliquots of the digest solution are reacted with either 4-bromo- or 4-chloro-1,2-diaminobenzene to quantitatively form the corresponding 2,1,3-benzoselenadiazole. Recovery of added selenite to a fish meal sample was 95% for the bromo derivative and 101% for the chloro derivative. Different portions of a well mixed fish meal sample were analyzed in independent laboratories by the fluorometric method and by atomic absorption spectrophotometry (hydride generation). The following mean values (microgram/g) were found: present method 1.89, fluorometric method 1.91, atomic absorption method 2.1. The lower limit of detection for the method described was 13 ng, using the bromo derivative, and 27 ng, using the chloro derivative.

摘要

本文描述了一种用于气相色谱法测定海洋生物材料中痕量硒的方法。该方法基于硒(IV)与溴代和氯代的1,2 - 二氨基苯的反应。如此形成的苯并硒二唑对电子捕获检测敏感。样品在硝酸 - 高氯酸混合物中消化,硒被还原为IV氧化态。消化液的不同等分试样与4 - 溴 - 或4 - 氯 - 1,2 - 二氨基苯反应,以定量形成相应的2,1,3 - 苯并硒二唑。添加到鱼粉样品中的亚硒酸盐,对于溴代衍生物的回收率为95%,对于氯代衍生物为101%。在独立实验室中,通过荧光法和原子吸收分光光度法(氢化物发生)对充分混合的鱼粉样品的不同部分进行了分析。得到以下平均值(微克/克):本方法为1.89,荧光法为1.91,原子吸收法为2.1。所述方法的检测下限,使用溴代衍生物时为13纳克,使用氯代衍生物时为27纳克。

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