Zhang Yanan, Chen Beibei, Wu Shaowei, He Man, Hu Bin
Key Laboratory of Analytical Chemistry for Biology and Medicine (Ministry of Education), Department of Chemistry, Wuhan University, Wuhan 430072, China.
College of Chemistry and Environmental Engineering, Hubei Institute for Nationalities, Enshi 445000, China.
Talanta. 2016 Jul 1;154:474-80. doi: 10.1016/j.talanta.2016.04.003. Epub 2016 Apr 4.
In this paper, a method of graphene oxide (GO)-TiO2 composite solid phase extraction followed by graphite furnace atomic absorption spectrometry (GFAAS) detection was proposed for the speciation of inorganic selenium in environmental waters. The adsorption behavior of inorganic Se(IV) and Se(VI) on the GO-TiO2(1:1) composite was investigated. It was found that Se(IV) was quantitatively retained on the GO-TiO2 composites within a wide pH range of 0.5-10, while Se(VI) was quantitatively adsorbed on GO-TiO2(1:1) composite at pH 0.5-2, and no obvious adsorption of Se(VI) within the pH range of 4-10 was found. By selecting pH 6.0, Se(IV) could be easily determined. After reduction of Se(VI), total Se was determined by the proposed method, and Se(VI) was calculated as the difference between the total Se and Se(IV). The factors affecting the separation/preconcentration of Se(IV) and Se(VI) were studied. Under the optimum conditions, the isothermal adsorption of Se(IV) on the GO-TiO2(1:1) composite fitted Langmuir model; a linear range over 0.1-12ngmL(-1) was obtained. The limit of detection (LOD) and precision of the method for Se(IV) was 0.04ngmL(-1) and 9.4% (cSe(IV)=0.5ngmL(-1), n=7), respectively. In order to verify the accuracy of the method, a standard water sample (GSBZ50031-94) was analyzed, and the determined value was in a good agreement to the certified value. The established method was applied to inorganic Se speciation in environmental water samples and the recovery of 87.4-102% was obtained for the spiked samples.
本文提出了一种采用氧化石墨烯(GO)-TiO₂ 复合固相萃取结合石墨炉原子吸收光谱法(GFAAS)检测的方法,用于环境水样中无机硒的形态分析。研究了无机硒(IV)和硒(VI)在 GO-TiO₂(1:1)复合材料上的吸附行为。结果表明,在 0.5 - 10 的宽 pH 范围内,Se(IV) 能被定量保留在 GO-TiO₂ 复合材料上;而在 pH 为 0.5 - 2 时,Se(VI) 能被定量吸附在 GO-TiO₂(1:1)复合材料上,在 4 - 10 的 pH 范围内未发现 Se(VI) 有明显吸附。选择 pH 6.0 时,可轻松测定 Se(IV)。将 Se(VI) 还原后,用该方法测定总硒,Se(VI) 通过总硒与 Se(IV) 的差值计算得出。研究了影响 Se(IV) 和 Se(VI) 分离/预富集的因素。在最佳条件下,Se(IV) 在 GO-TiO₂(1:1)复合材料上的等温吸附符合朗缪尔模型;获得了 0.1 - 12 ng mL⁻¹ 的线性范围。该方法对 Se(IV) 的检测限(LOD)和精密度分别为 0.04 ng mL⁻¹ 和 9.4%(cSe(IV)=0.5 ng mL⁻¹,n = 7)。为验证该方法的准确性,分析了标准水样(GSBZ50031 - 94),测定值与认证值吻合良好。所建立的方法应用于环境水样中无机硒的形态分析,加标样品的回收率为 87.4 - 102%。