Direct Determination of Lead in Foods by Solid Sampling Electrothermal Vaporization Atomic Fluorescence Spectrometry

• DOI: 10.2116/analsci.32.1007
• Publication Date: 2016-09-09T22:08:06Z
• Authors: Derong Shang; Yanfang Zhao; Yuxiu Zhai; Jinsong Ning; Delin Duan; Yongdong Zhou
• Keywords: Spectrometry, Fluorescence; Lead; Limit of Detection; Calibration; Analytic Sample Preparation Methods; Food Contamination; Volatilization; 01 natural sciences; 0104 chemical sciences

A solid sampling method for the determination of lead in foods (including grains, vegetables and seafoods) using electrothermal vaporization atomic fluorescence spectrometry was established. The method introduced samples using electrothermal vaporization by quartz furnace and used on-line ashing and vaporization to remove matrix interferences for the specific trap of lead. It was proven by the certified reference material (CRM) and the recovery rate of the standards that the electrothermal vaporization was stable and there was no effect for sampling difference. The best operating program and parameters for the new method included ashing (850°C, 160 s), vaporization and trap (1050°C, 80 s; 800°C, 10 s), release (800°C, 10 s), and mixed Ar + H2 (85:15%, v/v) as carrier gas with flow rate of 500 mL/min. The relative standard deviations of repeated Pb measurements in CRMs were all below 5.0%, and the recovery rate ranged from 90.0 - 110.0%. The limit of detection (LOD) for the new method was 3.0 pg and the limit of quantification (LOQ) was 10.0 pg. The total time of analysis was less than 6 min. No significant differences existed between the results measured by the new method and microwave ICP-MS.