Chen Qing-hui, Wan Yao-yu, Li Qian, Yao Jun-xue
Guang Pu Xue Yu Guang Pu Fen Xi. 2016 Oct;36(10):3351-4.
A separation/preconcentration procedure with coprecipitation has been proposed for the flame atomic absorption spectrometric (FAAS) determination of cadmium at trace level in food and environmental samples. Manganese(Ⅱ) was used as a carrier which chelated with 2-(5-bromo-2-pyridylazo)-5-diethylaminophenol to detect the content of trace cadmium in shrimp and shell fish samples with flame atomic absorption spectrometry for the first time. The precipitate could be easily dissolved with concentrated nitric acid. The optimum coprecipitation of this new method including the amount of reagent, amount of manganese(Ⅱ), the pH, and the standing time of the precipitate had been confirmed for the quantitative recoveries of the analytes. The effect of matrix ions and the interference of co-existing ions were also evaluated. Under the experimental conditions established by the optimization step, the system of Mn(Ⅱ)-5-Br-PADAP was able to overcome the matrix interference which showed the effect of separation and enrichment well. The linear range of cadmium content was determined to be 0.1~1.0 mg·L-1. The sensitivity and the relative standard deviation(RSD) were found 0.147(mg·L-1)-1, 0.73%, respectively. The optimum procedure allows the determination of cadmium with limit of detection of 4.27 μg·L-1. The complexity of preprocessing was determined by the complexity of food samples. So the differences of cadmium content in the samples between the direct determination with atomic absorption spectrometry and the measurement after coprecipitation were examined, which providedevidences for the superiority of the system again. Cadmium in shell fish and shrimp samples were 1.85 mg·kg-1 and 1.74 mg·kg-1, which in line with international standards of the Codex Alimentarius Commission(CAC). The credibility of the method was evaluated by standard additional method and recovery experiments. The standard addition recoveries of sample and RSDs of the method were in the range of 99.9%~100.3% and 0.15%~0.83%. The results of recovery experiment showed that the presented coprecipitation procedure had good repetition, high accuracy. In addition, with the method, we could draw conclusions that the experiments were simple and rapid. The developed method described in the literature was successfully applied for the determination of trace cadmium in shrimp and shell fish samples with satisfactory results.
提出了一种共沉淀分离/预富集方法,用于火焰原子吸收光谱法(FAAS)测定食品和环境样品中的痕量镉。首次以锰(Ⅱ)为载体,使其与2-(5-溴-2-吡啶偶氮)-5-二乙氨基苯酚螯合,采用火焰原子吸收光谱法检测虾和贝类样品中痕量镉的含量。沉淀可用浓硝酸轻松溶解。已确定该新方法的最佳共沉淀条件,包括试剂用量、锰(Ⅱ)用量、pH值和沉淀静置时间,以实现分析物的定量回收。还评估了基体离子的影响和共存离子的干扰。在优化步骤确定的实验条件下,Mn(Ⅱ)-5-Br-PADAP体系能够克服基体干扰,具有良好的分离和富集效果。镉含量的线性范围为0.1~1.0 mg·L-1。灵敏度和相对标准偏差(RSD)分别为0.147(mg·L-1)-1、0.73%。最佳方法的镉检测限为4.27 μg·L-1。预处理的复杂性取决于食品样品的复杂性。因此,研究了原子吸收光谱法直接测定样品与共沉淀后测定样品中镉含量的差异,再次证明了该体系的优越性。虾和贝类样品中的镉含量分别为1.85 mg·kg-1和1.74 mg·kg-1,符合食品法典委员会(CAC)的国际标准。通过标准加入法和回收率实验评估了该方法的可信度。样品的标准加入回收率和该方法的RSD在99.9%~100.3%和0.1