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Selenium speciation in tea by dispersive liquid-liquid microextraction coupled to high-performance liquid chromatography after derivatization with 2,3-diaminonaphthalene.
Zhou, Qingxiang; Lei, Man; Li, Jing; Wang, Mengyun; Zhao, Danchen; Xing, An; Zhao, Kuifu.
Afiliação
  • Zhou Q; Beijing Key Laboratory of Oil and Gas Pollution Control, College of Geosciences, China University of Petroleum Beijing, Beijing, China.
  • Lei M; Beijing Key Laboratory of Oil and Gas Pollution Control, College of Geosciences, China University of Petroleum Beijing, Beijing, China.
  • Li J; Beijing Key Laboratory of Oil and Gas Pollution Control, College of Geosciences, China University of Petroleum Beijing, Beijing, China.
  • Wang M; Beijing Key Laboratory of Oil and Gas Pollution Control, College of Geosciences, China University of Petroleum Beijing, Beijing, China.
  • Zhao D; Beijing Key Laboratory of Oil and Gas Pollution Control, College of Geosciences, China University of Petroleum Beijing, Beijing, China.
  • Xing A; Beijing Key Laboratory of Oil and Gas Pollution Control, College of Geosciences, China University of Petroleum Beijing, Beijing, China.
  • Zhao K; Beijing Key Laboratory of Oil and Gas Pollution Control, College of Geosciences, China University of Petroleum Beijing, Beijing, China.
J Sep Sci ; 38(9): 1577-83, 2015 May.
Article em En | MEDLINE | ID: mdl-25677605
ABSTRACT
Selenium is an important element for human health, and it is present in many natural drinks and foods. Present study described a new method using dispersive liquid-liquid microextraction prior to high-performance liquid chromatography with a UV variable wavelength detector for the determination of the total selenium, Se(IV), Se(VI), and total organoselenium in tea samples. In the procedure, 2,3-diaminonaphthalene was used as the chelating reagent, 400 µL acetonitrile was used as the disperser solvent and 60 µL chlorobenzene was used as the extraction solvent. The complex of Se(IV) and 2,3-diaminonaphthalene in the final extracted phase was analyzed by high-performance liquid chromatography. The factors influencing the derivatization and microextraction were investigated. Under the optimal conditions, the limit of detection was 0.11 µg/L for Se(IV) and the linearity range was in the range of 0.5-40 µg/L. This method was successfully applied to the determination of selenium in four tea samples with spiked recoveries ranging from 91.3 to 100%.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Selênio / Chá / Compostos Organosselênicos / Microextração em Fase Líquida / 2-Naftilamina Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Selênio / Chá / Compostos Organosselênicos / Microextração em Fase Líquida / 2-Naftilamina Idioma: En Ano de publicação: 2015 Tipo de documento: Article