Universidade Federal da Bahia, Grupo de Pesquisa em Química e Quimiometria, CEP: 40170-270, Salvador, Bahia, Brazil.
Talanta. 2013 Mar 15;106:293-7. doi: 10.1016/j.talanta.2012.11.001. Epub 2012 Nov 8.
In this paper, a method for the determination of mercury in phosphate fertilizers using slurry sampling and cold vapor atomic absorption spectrometry (CV QT AAS) is proposed. Because mercury (II) ions form strong complexes with phosphor compounds, the formation of metallic mercury vapor requires the presence of lanthanum chloride as a release agent. Thiourea increases the amount of mercury that is extracted from the solid sample to the liquid phase of the slurry. The method is established using two steps. First, the slurry is prepared using the sample, lanthanum chloride, hydrochloric acid solution and thiourea solution and is sonicated for 20 min. Afterward, mercury vapor is generated using an aliquot of the slurry in the presence of the hydrochloric acid solution and isoamylic alcohol with sodium tetrahydroborate solution as the reducing agent. The experimental conditions for slurry preparation were optimized using two-level full factorial design involving the factors: thiourea and lanthanum chloride concentrations and the duration of sonication. The method allows the determination of mercury by external calibration using aqueous standards with limits of detection and quantification of 2.4 and 8.2 μg kg(-1), respectively, and precision, expressed as relative standard deviation, of 6.36 and 5.81% for two phosphate fertilizer samples with mercury concentrations of 0.24 and 0.57 mg kg(-1), respectively. The accuracy was confirmed by the analysis of a certified reference material of phosphate fertilizer that was provided by the National Institute of Standards & Technology (NIST). The method was applied to determine mercury in six commercial samples of phosphate fertilizers. The mercury content varied from 33.97 to 209.28 μg kg(-1). These samples were also analyzed employing inductively coupled plasma mass spectrometry (ICP-MS). The ICP-MS results were consistent with the results from our proposed method.
本文提出了一种利用浆态采样和冷蒸气原子吸收光谱法(CV AAS)测定磷肥中汞的方法。由于汞(II)离子与磷化合物形成强配合物,因此形成金属汞蒸气需要氯化镧作为释放剂。硫脲增加了从固相样品中提取到浆态液相中的汞量。该方法通过两步建立。首先,使用样品、氯化镧、盐酸溶液和硫脲溶液制备浆体,并进行 20 分钟的超声处理。然后,在盐酸溶液和异戊醇存在下,用硼氢化钠溶液作为还原剂,从浆体的一部分中生成汞蒸气。通过涉及硫脲和氯化镧浓度以及超声时间的两水平完全因子设计优化浆体制备的实验条件。该方法允许通过使用具有检测限和定量限分别为 2.4 和 8.2μgkg-1的水溶液标准品进行外部校准来测定汞,对于两个汞浓度分别为 0.24 和 0.57mgkg-1的磷肥样品,精密度(表示为相对标准偏差)分别为 6.36%和 5.81%。通过分析由国家标准与技术研究所(NIST)提供的磷肥认证参考物质来确认准确性。该方法应用于测定六种商业磷肥样品中的汞。汞含量从 33.97 到 209.28μgkg-1不等。这些样品也采用电感耦合等离子体质谱法(ICP-MS)进行分析。ICP-MS 结果与我们提出的方法的结果一致。