Martendal Edmar, Maltez Heloisa França, Carasek Eduardo
Departamento de Química, Universidade Federal de Santa Catarina, Florianópolis, SC 88040-900, Brazil.
J Hazard Mater. 2009 Jan 15;161(1):450-6. doi: 10.1016/j.jhazmat.2008.03.117. Epub 2008 Apr 1.
In this study a new method for chromium speciation in water using solid phase extraction coupled to a flow injection system and flame atomic absorption spectrometry was developed. The adsorption behavior of Cr(III) and Cr(VI) on Nb2O5-SiO2 allowed the selective separation of Cr(III) from Cr(VI) in the pH range of 6-9. Thus, a method for Cr(III) preconcentration and extraction using Nb2O5-SiO2 was developed. Total chromium was determined after the reduction of Cr(VI) to Cr(III) using sodium sulfite in acidic medium. The operational variables of the preconcentration and reduction procedures were optimized through full factorial and Doehlert designs. The limit of detection for Cr(III) was 0.34microgL(-1) and the precision was below 4.6%. Results for recovery tests using different environmental samples were between 90 and 105%. Certified reference materials (NIST 1640 and NIST 1643e) were analyzed in order to check the accuracy of the proposed method, and the results were in agreement with the certified values.
在本研究中,开发了一种结合固相萃取、流动注射系统和火焰原子吸收光谱法的水中铬形态分析新方法。Cr(III)和Cr(VI)在Nb2O5-SiO2上的吸附行为使得在pH值为6 - 9的范围内能够将Cr(III)与Cr(VI)选择性分离。因此,开发了一种使用Nb2O5-SiO2对Cr(III)进行预富集和萃取的方法。在酸性介质中使用亚硫酸钠将Cr(VI)还原为Cr(III)后测定总铬。通过全因子设计和Doehlert设计对预富集和还原程序的操作变量进行了优化。Cr(III)的检测限为0.34μg L(-1),精密度低于4.6%。使用不同环境样品进行回收率测试的结果在90%至105%之间。分析了标准参考物质(NIST 1640和NIST 1643e)以检验所提方法的准确性,结果与认证值一致。