Mirza Muhammed Aslam, Khuhawar Muhammad Yar, Arain Rafee
Dr. M. A. Kazi Institute of Chemistry, University of Sindh, Jamshoro, Pakistan.
Electrophoresis. 2008 Feb;29(3):597-603. doi: 10.1002/elps.200700414.
An analytical procedure has been developed for the separation of dioxouranium(VI), iron(III), copper(II), nickel(II), cobalt(II), cobalt(III), palladium(II), and thorium(IV) by MEKC using N,N'-ethylene bis(salicylaldimine) (H(2)SA(2)en) as a complexing reagent with total runtime <4.5 min. SDS was used as micellar medium at pH 8 with sodium tetraborate buffer (0.1 M). An uncoated fused-silica capillary with an effective length of 50 cm x 75 microm id was used with an applied voltage of 30 kV with photodiode array detection at 231 nm. Linear calibrations were obtained within 0.111-1000 microg/mL of each element with LODs within 37-325 ng/mL. The developed method was tested for analysis of uranium ore samples indicating its presence within 103-1789 microg/g with RSD within 0.79-1.87%. Likewise copper, nickel, and iron in their combined matrix were also simultaneously determined with RSD 0.4-1.6% (n = 6).
已开发出一种分析方法,通过胶束电动毛细管色谱法(MEKC),以N,N'-亚乙基双(水杨醛亚胺)(H₂SA₂en)作为络合剂,在总运行时间小于4.5分钟的条件下分离双氧铀(VI)、铁(III)、铜(II)、镍(II)、钴(II)、钴(III)、钯(II)和钍(IV)。在pH 8的条件下,使用硼酸钠缓冲液(0.1 M)中的十二烷基硫酸钠(SDS)作为胶束介质。使用有效长度为50 cm×内径75 μm的未涂层熔融石英毛细管,施加电压30 kV,在231 nm处采用光电二极管阵列检测。各元素在0.111 - 1000 μg/mL范围内获得线性校准曲线,检测限在37 - 325 ng/mL范围内。所开发的方法用于分析铀矿石样品,结果表明铀含量在103 - 1789 μg/g之间,相对标准偏差(RSD)在0.79 - 1.87%之间。同样,在其混合基质中的铜、镍和铁也能同时测定,RSD为0.4 - 1.6%(n = 6)。