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1.
China Pharmacist ; (12): 1965-1968, 2016.
Article in Chinese | WPRIM | ID: wpr-503255

ABSTRACT

Objective:To establish the analysis method for the determination of Ni, Cu and Zn in aluminum food packaging mate-rials by inductively coupled plasma atomic emission spectrometry ( ICP-AES) . Methods: A small amount of EDTA was added to the test solution till the concentration at 0. 010 0 mol·L-1 and the pH value was adjusted to 5. 0. Strong acid cation exchange fibers were used for the assisted extraction of Al3+ with ultrasonic. Al3+ could not quickly form a complex anion with EDTA, so it was adsorbed by the strong acid cation exchange fibers. Cu2+, Ni2+ and Zn2+ could form complex anions with EDTA rapidly, so they could not be ad-sorbed by the strong acid cation exchange fibers and were left in the solution to be determined. Results:After the separation, the con-tents of Cu, Ni and Zn were not lost, and the content of residual aluminum was about 170 times of that of Cu, Ni and Zn, which had not interferece with the determination of Cu, Ni and Zn. The sample standard addition recovery was within the range of 98. 3%-104%with RSD of 0. 2%-2. 5%(n=5). The relative errors between the measured values and the certified values of standard substances were less than 5. 0%. Conclusion:The proposed method can be successfully applied in the separation and determination of Cu, Ni and Zn in aluminum cans, barbecue aluminum foil and standard substances.

2.
Article in Chinese | WPRIM | ID: wpr-403818

ABSTRACT

A comprehensive analytical method based on liquid chromatography tandem mass spectrometry has been developed for the determination of nonylphenol, octylphenol and bisphenol A in textiles and food packaging) materials. Various textile and food packaging material samples were extracted under the conditions of 10.3 MPa and 120 ℃ by accelerated solvent extraction method with two static cycles using ethanol as the extraction) solvent. The extract was cleaned up by Supelclean Envi-Carb solid phase extraction cartridge. Qualitative) and quantitative analyses were carried out for the analytes under the multiple reaction monitoring(MRM) mode after the chromatographic separation on Waters XBridge C_(18))(150 mm×2.1 mm, 3.5 μm) column) with methanol-0.1% NH_4OH gradient elution. The limits of detection(LODs) for alkylphenol, octyphenol and bisphenol A were 0.5 μg/kg. The mean recoveries for textile samples at the spiked level of 0.5-10 μg/kg were 86.9%-92.5%, with the relative standard deviation less than 9.1%. The mean recoveries for food packaging material samples at the spiked level of 0.5-10 μg/kg were 87.8%-93.0%, with the relative standard deviation less than 8.8%. The method is accurate, simple, rapid, and adapts to the inspection of nonylphenol, octylphenol and bisphenol A in textiles and food packaging materials.

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