Dokuz Eylul University, Faculty of Sciences and Arts, Chemistry Department, Kaynaklar Campus, 35160 Izmir, Turkey.
Talanta. 2011 Mar 15;84(1):212-5. doi: 10.1016/j.talanta.2011.01.006. Epub 2011 Jan 15.
A new method based on microcolumn packed with ionic liquid-modified silica combined with flame atomic absorption spectrometry has been developed for the determination of lead in environmental samples. Several factors influencing the preconcentration efficiency of lead and its subsequent determination, such as pH of the sample, flow rate, mass of ionic liquid, and interfering effect, have been investigated. Lead could be quantitatively retained by ionic liquid-modified silica in the pH range of 5-7, and then eluted completely with 3.0 mL 1.0 mol L(-1) HCl. The detection limit of this method for lead was 0.7 μg L(-1) with preconcentration factor of 185, and the relative standard deviation (RSD) was 4.2% at 0.1 μg mL(-1) Pb(II). This method has been applied for the determination of trace amount of lead in NIST standard reference material 2709 (San Joaquin Soil) and river water samples with satisfactory results.
基于微柱填充离子液体改性硅胶结合火焰原子吸收光谱法,建立了一种测定环境样品中铅的新方法。考察了影响铅的预富集效率及其后续测定的多种因素,如样品 pH 值、流速、离子液体质量和干扰效应。在 pH 值为 5-7 的范围内,铅可以被离子液体改性硅胶定量保留,然后用 3.0 mL 1.0 mol L(-1) HCl 完全洗脱。该方法对铅的检测限为 0.7 μg L(-1),富集因子为 185,在 0.1 μg mL(-1) Pb(II)时相对标准偏差(RSD)为 4.2%。该方法已应用于 NIST 标准参考物质 2709(圣华金土壤)和河水样品中痕量铅的测定,结果令人满意。