Padarauskas A V, Kazlauskiene L G
Department of Analytical Chemistry, University of Vilnius, 2734 Vilnius, Lithuania.
Talanta. 1993 Jun;40(6):827-30. doi: 10.1016/0039-9140(93)80037-r.
Ion-pair chromatography (IPC) with conductometric detection was investigated as a precise and selective analytical method for the determination of chromium in electro-plating solutions and waste waters. Chromatographic parameters were optimized for separation of Cr(VI) and SO(2-)(4). The analytical column (100 x 6 mm) was packed with 10 mum silasorb C(18) (Czechoslovakia). Tetrabutylammonium butyrate (TBAB), at pH 7.0 in acetonitrile-water (18:82 v/v) mixture, was used as the eluent. Two samples of solution are taken for the analysis. In the first of them the amount of Cr(VI) is determined, in the second one Cr(III) is oxidized to Cr(VI) with H(2)O(2) in alkaline medium and the total amount of Cr is determined. From the difference of the two obtained results the concentration of Cr(III) is calculated. The detection limit of Cr(VI) is 0.1 mug/ml and the relative standard deviation (at the 1.0 mug/ml) is 4.0%. The IPC results for chromium agreed closely with these obtained by spectrophotometry.
研究了采用电导检测的离子对色谱法(IPC)作为测定电镀液和废水中铬的精确且选择性的分析方法。对用于分离Cr(VI)和SO(4)(2-)的色谱参数进行了优化。分析柱(100×6 mm)填充有10μm的硅烷化硅胶C(18)(捷克斯洛伐克)。在pH 7.0的乙腈 - 水(18:82 v/v)混合物中,使用丁酸四丁基铵(TBAB)作为洗脱液。取两份溶液样品进行分析。在第一份样品中测定Cr(VI)的含量,在第二份样品中,在碱性介质中用H(2)O(2)将Cr(III)氧化为Cr(VI),然后测定Cr的总量。根据两个所得结果的差值计算Cr(III)的浓度。Cr(VI)的检测限为0.1μg/ml,相对标准偏差(在1.0μg/ml时)为4.0%。铬的离子对色谱法结果与通过分光光度法获得的结果非常吻合。