4.5 Article

Rapid and Sensitive Determination of Dinotefuran Residue Based on Electrochemical Enhancement of β-cyclodextrin-Graphene Composite

期刊

ELECTROANALYSIS
卷 28, 期 7, 页码 1495-1503

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/elan.201501041

关键词

Dinotefuran; Electrochemical sensor; beta-cyclodextrin-graphene composite; Millet samples; Determination

资金

  1. National Natural Science Foundation of China [31000831]
  2. National Science Foundation for Post-doctoral Scientists of China [20090450478]
  3. Youth Science Fund Project of Heilongjiang Province [QC2013C026]
  4. Natural Science Research and Innovation Funds of Harbin Institute of Technology [HIT.NSRIF.2008.30]
  5. Postdoctoral Science-Research Developmental Foundation of Heilongjiang Province [LBH-Q12085]

向作者/读者索取更多资源

A rapid method for sensitive voltammetric determination of dinotefuran residue was reported. The proposed method was based on the electrocatalytic reduction of dinotefuran on beta-cyclodextrin-graphene composite modified glassy carbon electrode (beta-CD-rGO/GCE), giving rise to a higher reduction signal to dinotefuran relative to the bare (GCE) and graphene modified electrode (rGO/GCE). Moreover, a further signal enhancement was observed when the modified electrode incubated in solution at low temperature (0 degrees C) for a short time. The reduction mechanism and binding affinity were also discussed. The external standard calibration curve was obtained from linear sweep voltammetry in the range of 0.5 to 16.0 mu M with a detection limit of 0.10 mu M. In addition to optimization of pretreatment, this electrochemical method has been applied to the dinotefuran residue determination in millet samples with the detection limit of 0.01 mg kg(-1) and compared with an high performance liquid chromatography method. The proposed electrode and analysis methods were proven to be sensitive, accurate and rapid under the used conditions.

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