Liu Y, Ingle J D
Anal Chem. 1989 Mar 15;61(6):525-9. doi: 10.1021/ac00181a005.
A rapid method for determination of metal speciation based on an automated two-column ion exchange system is described. Two fractions of dissolved trace metal species are directly determined by on-line flame atomic absorption spectrophotometry after preconcentration by sequential columns of Chelex-100 chelating resin and AG MP-1 macroporous anion resin. A third fraction is determined by standard addition. Variables that affect the results obtained by the two-column system are studied by the use of model complexing agents. With a 10-mL sample loop, the sample throughput is 6 samples per hour and detection limits are 0.1 micrograms/L for Cu(II), 0.08 micrograms/L for Cd(II), and 0.2 micrograms/L for Zn(II). The method is used to determine the speciation of Cu(II), Cd(II), and Zn(II) in natural water samples.
本文描述了一种基于自动双柱离子交换系统测定金属形态的快速方法。溶解的痕量金属物种的两个部分通过Chelex-100螯合树脂和AG MP-1大孔阴离子树脂的连续柱预富集后,直接通过在线火焰原子吸收分光光度法测定。第三部分通过标准加入法测定。使用模型络合剂研究了影响双柱系统所得结果的变量。使用10 mL进样环时,每小时进样量为6个样品,铜(II)的检测限为0.1微克/升,镉(II)为0.08微克/升,锌(II)为0.2微克/升。该方法用于测定天然水样中铜(II)、镉(II)和锌(II)的形态。