Fang Jing, Jiang Yan, Yan Xiu-Ping, Ni Zhe-Ming
State Key Laboratory of Functional Polymer Materials for Adsorption and Separation, Research Center for Analytical Sciences, College of Chemistry, Nankai University, Tianjin 300071, China.
Environ Sci Technol. 2005 Jan 1;39(1):288-92. doi: 10.1021/es049303+.
There is a growing concern about the effect of palladium on human health because of the toxicity and increasing occurrence of palladium as a result of its extensive use in automotive catalytic converters. Development of reliable analytical methodologies for the determination of palladium in environmental materials is of great importance for critical evaluation of the possible risks for human health. In this work, a displacement solid-phase extraction technique was developed and online coupled to electrothermal atomic absorption spectrometry (ETAAS) for selective and sensitive determination of trace palladium in environmental samples without need of any special selective complexing agents, selective sorbents, and masking agents. The developed methodology involved the online formation of copper pyrrolidine dithiocarbamate (Cu-PDC), and the resultant Cu-PDC was extracted onto a microcolumn packed with the sorbent from a cigarette filter. Trace Pd(II) was selectively preconcentrated through loading the sample solution onto the microcolumn by online displacement reaction between Pd(II) and the extracted Cu-PDC on the microcolumn. The retained analyte was subsequently eluted with 40 microL of ethanol for online ETAAS determination. Interferences from coexisting heavy metal ions with lower stability of their PDC complexes relative to Cu-PDC were minimized. The tolerable concentrations of Cd-(II), Fe(III), Co(II), Mn(II), Cr(III), and Zn(II) were up to 2, 6, 40, 2, 1.5, and at least 100 mg L(-1), respectively. Compared with conventional solid-phase extraction methodology, the developed displacement solid-phase extraction protocol gave 2-4 orders of magnitude improvement in the maximum tolerable concentrations of coexisting heavy metal ions. With the consumption of only 2.8 mL of sample solution, an enhancement factor of 52 and a detection limit (3sigma) of 18 ng L(-1) were achieved at a sample throughput of 30 samples h(-1). The precision (RSD, n = 13) was 2.5% at the 1 microg L(-1) level. The present methodology was successfully applied to selective determination of trace palladium in local road dusts and roadside soils.
由于钯的毒性以及其在汽车催化转化器中的广泛使用导致其出现频率增加,人们对钯对人体健康的影响日益关注。开发可靠的分析方法来测定环境材料中的钯对于严格评估对人体健康可能存在的风险非常重要。在这项工作中,开发了一种置换固相萃取技术,并将其在线耦合到电热原子吸收光谱法(ETAAS),用于选择性和灵敏地测定环境样品中的痕量钯,无需任何特殊的选择性络合剂、选择性吸附剂和掩蔽剂。所开发的方法涉及在线形成吡咯烷二硫代氨基甲酸铜(Cu-PDC),并将所得的Cu-PDC从香烟滤嘴中萃取到装有吸附剂的微柱上。痕量Pd(II)通过将样品溶液加载到微柱上,通过Pd(II)与微柱上萃取的Cu-PDC之间的在线置换反应进行选择性预富集。随后用40 μL乙醇洗脱保留的分析物,用于在线ETAAS测定。与Cu-PDC相比,其PDC络合物稳定性较低的共存重金属离子的干扰被降至最低。Cd(II)、Fe(III)、Co(II)、Mn(II)、Cr(III)和Zn(II)的可耐受浓度分别高达2、6、40、2、1.5和至少100 mg L(-1)。与传统固相萃取方法相比,所开发的置换固相萃取方案在共存重金属离子的最大可耐受浓度方面提高了2-4个数量级。仅消耗2.8 mL样品溶液,在30个样品 h(-1)的样品通量下,实现了52的富集因子和18 ng L(-1)的检测限(3σ)。在1 μg L(-1)水平下,精密度(RSD,n = 13)为2.5%。本方法成功应用于当地道路灰尘和路边土壤中痕量钯的选择性测定。