Department of Chemistry, Lanzhou University, Lanzhou 730000, PR China.
Anal Chim Acta. 2010 Mar 24;663(2):213-7. doi: 10.1016/j.aca.2010.01.057. Epub 2010 Feb 6.
A new method that utilizes asparagine modified attapulgite as a solid phase extractant has been developed for preconcentration of trace Fe(III) prior to the measurement by inductively coupled plasma optical emission spectrometry. Characterization of the surface modification was performed on the basis of Fourier transform infrared spectra. The separation/preconcentration conditions of the analyte were investigated, including the pH value, the shaking time, the sample fl ow rate and volume, the elution condition and the interfering ions. At pH 4, the new adsorbent had relatively high capacity and enrichment factor compared to other methods reported so far. The adsorbed Fe(III) was quantitatively eluted by 2 mL of 0.5 mol L(-1) HCl. Common coexisting ions did not interfere with the separation. The detection limit of the method was 0.19 microg L(-1). The relative standard deviation was 3.4% (n=8) which indicated that the method had good precision for the analysis of trace Fe(III) in solution samples. The method was validated using two certified reference materials and has been applied for the determination of trace Fe(III) in biological and natural water samples with satisfactory results.
一种新的方法,利用天冬酰胺修饰凹凸棒石作为固相萃取剂,已被开发用于痕量 Fe(III)的预浓缩,然后通过电感耦合等离子体发射光谱法进行测量。根据傅里叶变换红外光谱对表面修饰进行了表征。研究了分析物的分离/预浓缩条件,包括 pH 值、摇床时间、样品流速和体积、洗脱条件和干扰离子。在 pH 值为 4 时,与迄今为止报道的其他方法相比,新吸附剂具有相对较高的容量和富集因子。吸附的 Fe(III)可通过 2 mL 0.5 mol L(-1) HCl 定量洗脱。常见共存离子不干扰分离。该方法的检测限为 0.19 microg L(-1)。相对标准偏差为 3.4%(n=8),表明该方法对溶液样品中痕量 Fe(III)的分析具有良好的精密度。该方法已使用两种认证参考物质进行验证,并已应用于生物和天然水样中痕量 Fe(III)的测定,结果令人满意。