摘要
目的:建立石墨炉原子吸收法测定食品铅的新技术。方法:采用硝酸+硫酸+双氧水消解样品,再用氢碘酸还原剩余硫酸;选用磷酸二氢铵(2%)+氯化钯(0.4%)作基体改进剂,提高灰化温度,有效去除基体干扰,在选定的仪器条件下测定食品中铅。结果:铅在3~120μg/L范围内线性良好,方法定量限为0.0028 mg/kg,加标回收率为90.3%~107%,相对标准偏差(RSD)为1.2%~7.5%。结论:本法简便、快速、准确,灵敏度及精密度高,适用于食品中铅的测定。
Objective:To develop a method for the determination of lead in food by GFAAS.Methods:The samples were digested by a mixture of nitric acid,sulfuric acid and hydrogen peroxide and then the hydrogen periodate restored the remaining sulfuric acid.Ammonium dihydrogen phosphate(2%) and PdCI2(0.4%),as a matrix modifier,can improve cineration temperature and effectively remove matrix interference.Results:The linear range was 3~120 μg/L,quantification limit was 0.0028 mg/kg,recoveries were 90.3%~107% with the relative standard deviation(RSD) of 1.2%~7.5% for the method.Conclusion:The method was simple,rapid,accurate and sensitive.It has been successfully applied to determination of lead of in food.
出处
《中国卫生检验杂志》
CAS
2009年第12期2822-2823,共2页
Chinese Journal of Health Laboratory Technology