Department of Chemistry, Faculty of Arts and Sciences, Nevsehir University, Nevsehir 50300, Turkey.
Talanta. 2011 Apr 15;84(2):319-23. doi: 10.1016/j.talanta.2011.01.020. Epub 2011 Jan 15.
A trace element preconcentration procedure is described utilizing a minicolumn of yeast (Yamadazyma spartinae) immobilized TiO(2) nanoparticles for determination of Cr, Cu, Fe, Mn, Ni and Zn from water samples by inductively coupled plasma atomic emission spectrometry. The elements were quantitatively retained on the column between pH 6 and 8. Elution was made with 5% (v/v) HNO(3) solution. Recoveries ranged from 98 ± 2 (Cr) to 100 ± 4 (Zn) for preconcentration of 50 mL multielement solution (50 μg L(-1)). The column made up of 100mg sorbent (yeast immobilized TiO(2) NP) offers a capacity to preconcentrate up to 500 mL of sample solution to achieve an enrichment factor of 250 with 2 mL of 5% (v/v) HNO(3) eluent. The detection limits obtained from preconcentration of 50 mL blank solutions (5%, v/v, HNO(3), n=11) were 0.17, 0.45, 0.25, 0.15, 0.33 and 0.10 μg L(-1) for Cr, Cu, Fe, Mn, Ni and Zn, respectively. Relative standard deviation (RSD) for five replicate analyses was better than 5%. The retention of the elements was not affected from up to 500 μg L(-1) Na(+) and K(+) (as chlorides), 100 μg L(-1) Ca(2+) (as nitrate) and 50 μg L(-1) Mg(2+) (as sulfate). The method was validated by analysis of freshwater standard reference material (SRM 1643e) and applied to the determination of the elements from tap water and lake water samples.
一种微量元素预浓缩程序,利用固定化 TiO2 纳米粒子的酵母(Yamadazyma spartinae)小柱,通过电感耦合等离子体原子发射光谱法从水样中测定 Cr、Cu、Fe、Mn、Ni 和 Zn。元素在 pH 6 至 8 之间定量保留在柱上。用 5%(v/v)HNO3 溶液洗脱。对于 50mL 多元素溶液(50μg/L)的预浓缩,回收率范围为 98±2(Cr)至 100±4(Zn)。由 100mg 吸附剂(固定化 TiO2 NP 的酵母)组成的小柱能够预浓缩多达 500mL 的样品溶液,用 2mL 5%(v/v)HNO3 洗脱剂达到 250 的富集因子。用 50mL 空白溶液(5%,v/v,HNO3,n=11)预浓缩得到的检测限分别为 0.17、0.45、0.25、0.15、0.33 和 0.10μg/L,用于 Cr、Cu、Fe、Mn、Ni 和 Zn。五次重复分析的相对标准偏差(RSD)优于 5%。元素的保留不受高达 500μg/L(以氯化物计)的 Na+和 K+、100μg/L(以硝酸盐计)的 Ca2+和 50μg/L(以硫酸盐计)的 Mg2+的影响。该方法通过对淡水标准参考物质(SRM 1643e)的分析进行了验证,并应用于自来水中元素的测定和湖水样品。