Ellen G, Van Loon J W
National Institute of Public Health and Environmental Protection, Bilthoven, The Netherlands.
Food Addit Contam. 1990 Mar-Apr;7(2):265-73. doi: 10.1080/02652039009373891.
Two methods for the determination of cadmium and lead based on graphite furnace atomic absorption spectrometry (GFAAS) with Zeeman background correction are described. The main difference between the methods is the method of sample destruction, bomb digestion versus dry ashing. The precision and accuracy of the methods has been tested by analysing 16 different reference materials, with cadmium concentrations varying from 2.9 micrograms/kg to 2.7 mg/kg and lead concentrations from 44 micrograms/kg to 13.5 mg/kg. The methods produced results which differ, with a few exceptions, less than 10% from the certified contents, with relative standard deviations of around 5%. The methods are not difficult to carry out, are not very laborious and without modifications are applicable to a large variety of products. The sample solutions obtained can also be used for the determination of other elements, e.g. Al, Cr, Cu, Hg, Mn, Ni and Zn. The detection limits, for test portions of 1 and 5 g (wet products) are 0.5-1 microgram/kg for cadmium and 5-20 micrograms/kg for lead.
介绍了两种基于带有塞曼背景校正的石墨炉原子吸收光谱法(GFAAS)测定镉和铅的方法。这两种方法的主要区别在于样品消解方法,即高压釜消解与干灰化。通过分析16种不同的标准物质对这些方法的精密度和准确度进行了测试,其中镉浓度从2.9微克/千克到2.7毫克/千克不等,铅浓度从44微克/千克到13.5毫克/千克不等。除了少数例外情况,这些方法得出的结果与认证含量的差异小于10%,相对标准偏差约为5%。这些方法不难实施,不太费力,无需修改即可适用于多种产品。所得的样品溶液还可用于测定其他元素,例如铝、铬、铜、汞、锰、镍和锌。对于1克和5克(湿产品)的试验份,镉的检测限为0.5 - 1微克/千克,铅的检测限为5 - 20微克/千克。