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Determination of anionic impurities in hexafluorosilicic acid by capillary zone electrophoresis

机译:毛细管区带电泳法测定六氟硅酸中的阴离子杂质

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This paper reports an alternative analytical methodology for the determination of chloride and sulphate impurities in hexafluorosilicic acid, FSA, using capillary zone electrophoresis. The influence of different electrophoretic and matrix variables on electrophoretic response was studied. Samples were injected hydrodynamically onto a fused silica capillary of 63.5 cm x 75 urn id, with an effective length of 55 cm. The capillary temperature was kept constant at 25 ± 1 °C throughout the experiments. A voltage of -25 kV was applied (in anionic mode). The electrophoretic zones were detected with a fixed-wavelength UV detector at 254 nm and a diode array detector at 254 and 370 nm. The final background electrolyte consisted of 20 mM sodium chromate at pH 8.0 containing 6% MeOH and 1.5 μM tetradecyltrimethylammonium hydroxide. In these electrophoretic conditions, the separation of chloride and sulphate anions is achieved in less than ten minutes. The introduction of a water gap before the sample injection increases considerably the capillary life. The electrophoretic method developed allows the determination of chloride and sulphate at mg L~(-1) concentration levels in industrial production FSA samples.
机译:本文报道了使用毛细管区带电泳测定六氟硅酸FSA中氯化物和硫酸盐杂质的另一种分析方法。研究了不同的电泳和基质变量对电泳响应的影响。流体动力学地将样品注入63.5 cm x 75 ur id的熔融石英毛细管上,有效长度为55 cm。在整个实验过程中,毛细管温度保持恒定在25±1°C。施加-25kV的电压(以阴离子模式)。电泳区使用254 nm的固定波长UV检测器和254和370 nm的二极管阵列检测器检测。最终的本底电解质由pH 8.0的20 mM铬酸钠组成,含有6%MeOH和1.5μM十四烷基三甲基氢氧化铵。在这些电泳条件下,氯离子和硫酸根阴离子的分离可在不到十分钟的时间内完成。在进样之前引入水隙会大大延长毛细管寿命。所开发的电泳方法可以测定工业生产FSA样品中Lg(-1)浓度水平下的氯化物和硫酸盐。

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