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顶空单滴微萃取与微量紫外可见分光光度法联用测定碘

Headspace single-drop microextraction coupled to microvolume UV-vis spectrophotometry for iodine determination.

作者信息

Pena-Pereira Francisco, Lavilla Isela, Bendicho Carlos

机构信息

Departamento de Química Analítica y Alimentaria, Area de Química Analítica, Facultad de Química, Universidad de Vigo, Campus As Lagoas-Marcosende s/n, 36310 Vigo, Spain.

出版信息

Anal Chim Acta. 2009 Jan 12;631(2):223-8. doi: 10.1016/j.aca.2008.10.048. Epub 2008 Oct 30.

DOI:10.1016/j.aca.2008.10.048
PMID:19084630
Abstract

Headspace single-drop microextraction has been combined with microvolume UV-vis spectrophotometry for iodine determination. Matrix separation and preconcentration of iodide following in situ volatile iodine generation and extraction into a microdrop of N,N'-dimethylformamide is performed. An exhaustive characterization of the microextraction system and the experimental variables affecting iodine generation from iodide was carried out. The procedure employed consisted of exposing 2.5 microL of N,N'-dimethylformamide to the headspace of a 10 mL acidic (H(2)SO(4) 2 molL(-1)) aqueous solution containing 1.7 molL(-1) Na(2)SO(4) for 7 min. Addition of 1 mL of H(2)O(2) 1 molL(-1) for in situ iodine generation was performed. The limit of detection was determined as 0.69 microgL(-1). The repeatability, expressed as relative standard deviation, was 4.7% (n=6). The calibration working range was from 5 to 200 microgL(-1) (r(2)=0.9991). The large preconcentration factor obtained, ca. 623 in only 7 min, compensate for the 10-fold loss in sensitivity caused by the decreased optical path, which results in improved detection limits as compared to spectrophotometric measurements carried out with conventional sample cells. The method was successfully applied to the determination of iodine in water, pharmaceutical and food samples.

摘要

顶空单滴微萃取已与微量紫外可见分光光度法联用用于碘的测定。通过原位生成挥发性碘并萃取到N,N'-二甲基甲酰胺微滴中,实现了碘化物的基体分离和预富集。对微萃取系统以及影响碘化物中碘生成的实验变量进行了详尽表征。所采用的步骤包括将2.5 μL N,N'-二甲基甲酰胺暴露于10 mL含有1.7 molL(-1) Na(2)SO(4)的酸性(2 molL(-1) H(2)SO(4))水溶液的顶空中7分钟。加入1 mL 1 molL(-1) H(2)O(2)进行原位碘生成。检测限确定为0.69 μgL(-1)。以相对标准偏差表示的重复性为4.7%(n = 6)。校准工作范围为5至200 μgL(-1)(r(2)=0.9991)。仅在7分钟内获得的大约623的大预富集因子,弥补了由于光程减小导致的灵敏度10倍损失,与使用传统样品池进行的分光光度测量相比,检测限得到了改善。该方法成功应用于水、药品和食品样品中碘的测定。

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