Welna Maja, Borkowska-Burnecka Jolanta, Popko Malgorzata
Wroclaw University of Technology, Faculty of Chemistry, Division of Analytical Chemistry and Chemical Metallurgy, Wybrzeze Wyspianskiego 27, 50-370 Wroclaw, Poland.
Wroclaw University of Technology, Faculty of Chemistry, Division of Analytical Chemistry and Chemical Metallurgy, Wybrzeze Wyspianskiego 27, 50-370 Wroclaw, Poland.
Talanta. 2015 Nov 1;144:953-9. doi: 10.1016/j.talanta.2015.07.058. Epub 2015 Jul 21.
Followed the current idea of simplified sample pretratmet before analysis we evaluated the procedure for the determination of Pb in calcium-rich materials such as dolomites after ultrasound- or microwave- assisted extraction with diluted acids using hydride generation inductively coupled plasma optical emission spectrometry (HG-ICP-OES). Corresponding Pb hydride was generated in the reaction of an acidified sample solution with NaBH4 after pre-oxidation of Pb(II) to Pb(IV) by K3[Fe(CN)6]. Several chemical (acidic media: HCl, HNO3 or CH3COOH, concentration of the reductant as well as type and concentration of oxidazing agents) and physical (reagents flow rates, reaction coil length) parameters affecting the efficiency of plumbane formation were optimized in order to improve the detectability of Pb using HG-ICP-OES. Limitation of the method derived from the matrix effects was pointed out. Employing Pb separation by HG technique allows the significant reduction of interferences caused by sample matrix constituents (mainly Ca and Mg), nevertheless they could not be overcame at all, hence calibration based on the standard addition method was recommended for Pb quantification in dolomites. Under the selected conditions, i.e. 0.3 mol L(-1) HCl, HNO3 or CH3COOH, 1.5% NaBH4 and 3.0% K3[Fe(CN)6] the limits of detection (LODs) between 2.3-5.6 μg L(-1) (3.4-6.8 μg L(-1) considering matrix effects) and the precision below 5% were achieved. The accuracy of the procedure was verified by analysis of certified reference materials (NCS DC70308 (Carbonate Rock) and NIST 14000 (Bone Ash)) and recovery test with satisfactory results of Pb recoveries ranging between 94-108% (CRMs analysis) and 92-114% (standard addition method). The applicability of the proposed method was demonstrated by the determination of Pb in dolomites used by different fertiliser factories.
遵循当前分析前简化样品预处理的理念,我们评估了采用氢化物发生电感耦合等离子体发射光谱法(HG-ICP-OES),在超声或微波辅助下用稀酸萃取后,测定白云石等富钙材料中铅的方法。在通过K3[Fe(CN)6]将Pb(II)预氧化为Pb(IV)后,酸化的样品溶液与NaBH4反应生成相应的铅氢化物。为了提高使用HG-ICP-OES测定铅的可检测性,对影响铅烷形成效率的几个化学参数(酸性介质:HCl、HNO3或CH3COOH、还原剂浓度以及氧化剂类型和浓度)和物理参数(试剂流速、反应线圈长度)进行了优化。指出了该方法受基体效应限制的问题。采用HG技术分离铅可显著减少样品基体成分(主要是Ca和Mg)引起的干扰,然而干扰无法完全消除,因此建议采用标准加入法进行白云石中铅的定量校准。在选定的条件下,即0.3 mol L(-1) HCl、HNO3或CH3COOH、1.5% NaBH4和3.0% K3[Fe(CN)6],检测限(LOD)在2.3 - 5.6 μg L(-1)之间(考虑基体效应时为3.4 - 6.8 μg L(-1)),精密度低于5%。通过分析有证标准物质(NCS DC70308(碳酸盐岩)和NIST 14000(骨灰))以及回收率测试验证了该方法的准确性,铅回收率在94 - 108%(有证标准物质分析)和92 - 114%(标准加入法)之间,结果令人满意。通过测定不同化肥厂使用的白云石中的铅,证明了所提出方法的适用性。