A chemiluminescence resonance energy transfer system composed of cobalt(II), luminol, hydrogen peroxide and CdTe quantum dots for highly sensitive determination of hydroquinone

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• 作者：Shuxia Xu ; Jialin Li ; Xianming Li ; Min Su ; Zeming Shi ; Ying Zeng…
• 关键词：Nonenzymatic assay ; Catalytic oxidation ; Surface modification ; Water analysis ; Transmission electron microscopy ; Interference ; Standard addition
• 刊名：Microchimica Acta
• 出版年：2016
• 出版时间：February 2016
• 年：2016
• 卷：183
• 期：2
• 页码：667-673
• 全文大小：1,043 KB
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• 作者单位：Shuxia Xu (1) (2)
  Jialin Li (1)
  Xianming Li (1)
  Min Su (1)
  Zeming Shi (3)
  Ying Zeng (1) (2)
  Shijun Ni (3)
  
  1. College of Material and Chemistry & Chemical Engineering, Chengdu University of Technology, Chengdu, 610059, China
  2. Mineral Resources Chemistry Key Laboratory of Sichuan Higher Education Institutions, Chengdu University of Technology, Chengdu, 610059, China
  3. College of Earth Sciences, Chengdu University of Technology, Chengdu, 610059, China
  
• 刊物类别：Chemistry and Materials Science
• 刊物主题：Chemistry
  Analytical Chemistry
  Inorganic Chemistry
  Physical Chemistry
  Characterization and Evaluation Materials
  Monitoring, Environmental Analysis and Environmental Ecotoxicology
  
• 出版者：Springer Wien
• ISSN：1436-5073

文摘

This article describes a nonenzymatic chemiluminescence resonance energy transfer (CRET) system for highly sensitive determination of hydroquinone. It was found that the Co(II)-catalyzed luminescence of luminol in pH 11.5 solution is transferred to CdTe quantum dots (QDs) via a CRET mechanism. Hydroquinone is oxidized by H₂O₂ to benzoquinone which quenches the fluorescence of the QDs. The enhancement is attributed to the adsorption of Co(II) on the surface of the negatively charged QDs. The CRET system was applied in an assay for hydroquinone that has a detection limit of 0.17 nmol L−1. The detection limit was lower by factors between 100 and 250,000 than earlier reported methods. The assay was successfully applied to the quantitation of hydroquinone in (spiked) water samples, with recoveries ranging from 95 % to 106 %, and relative standard deviations between 0.5 % and 2.4 %.