A novel method for the determination of trace copper in cereals by dispersive liquid-liquid microextraction based on solidification of floating organic drop coupled with flame atomic absorption spectrometry

Chun Xia Wu Qiu Hua Wu Chun Wang Zhi Wang

引用本文: Chun Xia Wu,  Qiu Hua Wu,  Chun Wang,  Zhi Wang. A novel method for the determination of trace copper in cereals by dispersive liquid-liquid microextraction based on solidification of floating organic drop coupled with flame atomic absorption spectrometry[J]. Chinese Chemical Letters, 2011, 22(4): 473-476. doi: 10.1016/j.cclet.2010.10.049 shu
Citation:  Chun Xia Wu,  Qiu Hua Wu,  Chun Wang,  Zhi Wang. A novel method for the determination of trace copper in cereals by dispersive liquid-liquid microextraction based on solidification of floating organic drop coupled with flame atomic absorption spectrometry[J]. Chinese Chemical Letters, 2011, 22(4): 473-476. doi: 10.1016/j.cclet.2010.10.049 shu

A novel method for the determination of trace copper in cereals by dispersive liquid-liquid microextraction based on solidification of floating organic drop coupled with flame atomic absorption spectrometry

  • 基金项目:

    This project is supported by the Natural Science Foundation of Hebei (No. B2010000657).

摘要: A novel, simple, rapid, efficient and environment-friendly method for the determination of trace copper in cereal samples was developed by using dispersive liquid-liquid microextraction based on solidification of floating organic drop (DLLME-SFO) followed by flame atomic absorption spectrometry. In the DLLME-SFO, copper was complexed with 8-hydroxy quinoline and extracted into a small volume of 1-dodecanol, which is of low density, low toxicity and proper melting point near room temperature. The experimental parameters affecting the extraction efficiency were investigated and optimized. Under the optimum conditions, the calibration graph exhibited linearity over the range of 0.5-500 ng/mL with the correlation coefficient (r) of 0.9996. The enrichment factor was 122 and the limit of detection was 0.1 ng/mL. The method was applied to the determination of copper in the complex matrix samples such as rice and millet with the recoveries for the spiked samples at 5.0 and 10.0 μg/g falling in the range of 92.0-98.0% and the relative standard deviation of 3.9-5.7%.

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  • 收稿日期:  2010-07-23
通讯作者: 陈斌, bchen63@163.com
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