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Microtitrimetry by controlled current potentiometric titration

机译:通过控制电流电位滴定法进行微量滴定

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The classical methods of titration require large volumes of chemicals. Microtritimetry is the method of choice since it utilizes small quantities of chemicals and yields less waste compared to other conventional methods. Thus it benefits both the analytical chemists and the environment. In this communication, microtitrimetry is performed by employing the technique of differential electrolytic potentiometry for the location of the end point. Oxidation-reduction titration using platinum electrodes is described. For the first time the endpoint for a sample of 1.0 μL of 0.10 M Fe(II) has been located by titration using a solution of Ce(IV). The optimum conditions such as volume of cerium ammonium sulfate added, current applied to polarize the electrodes in case of dc controlled current potentiometric titration (CCPT). The effect of changing the percentage bias of the square wave used to polarize the electrodes on the differential peak in case of ac CCPT has been investigated. The precision of this microtitrimetric method is also reported.
机译:经典的滴定方法需要大量的化学药品。与其他传统方法相比,微三脚架是一种选择的方法,因为它利用的化学物质量少,浪费少。因此,它对分析化学家和环境都有利。在这种交流中,微量滴定法是通过采用差分电解电位计技术对终点位置进行的。描述了使用铂电极的氧化还原滴定。首次通过使用Ce(IV)溶液进行滴定确定了1.0μL0.10 M Fe(II)样品的终点。最佳条件,例如添加的硫酸铈铵的体积,在直流控制电流电位滴定(CCPT)的情况下施加的电流极化电极。已经研究了在交流CCPT情况下改变用于极化电极的方波的百分比偏差对差分峰的影响。还报道了这种微量滴定方法的精度。

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