Minami Tomoharu, Atsumi Kousuke, Ueda Joichi
Faculty of Education, Kanazawa University, Kakumamachi, Kanazawa 920-1192, Japan.
Anal Sci. 2003 Feb;19(2):313-5. doi: 10.2116/analsci.19.313.
Trace amounts of cobalt and nickel in a water sample were quantitatively coprecipitated with scandium hydroxide at pH 8.0-10.5. Because the coprecipitant could be easily dissolved with 1 mol dm(-3) nitric acid, and the presence of up to 10 mg cm(-1) of scandium did not interfere with the graphite-furnace atomic absorption spectrometric determination of cobalt and nickel, the volume of the final solution prepared for the determination could be minimized down to 0.5 cm3. The concentration factor was 400-fold and the detection limits (signal to noise = 2) were 5.0 pg cm(-3) of cobalt and 10.0 pg cm(-3) of nickel in 200 cm3 of the initial sample solution. The 27 diverse ions investigated did not interfere with the determination in at least a 500-fold mass ratio to cobalt or nickel. The proposed method was successfully applied to the determination of trace amounts of cobalt and nickel in river-water samples.
在pH 8.0 - 10.5的条件下,水样中的痕量钴和镍与氢氧化钪定量共沉淀。由于共沉淀剂可轻松溶于1 mol dm(-3)的硝酸,且存在高达10 mg cm(-1)的钪并不干扰石墨炉原子吸收光谱法对钴和镍的测定,因此用于测定的最终溶液体积可最小化至0.5 cm3。浓缩因子为400倍,在200 cm3的初始样品溶液中,钴的检测限(信噪比 = 2)为5.0 pg cm(-3),镍的检测限为10.0 pg cm(-3)。所研究的27种不同离子至少在与钴或镍的质量比为500倍时不干扰测定。该方法成功应用于河水样品中痕量钴和镍的测定。