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COMPARISON OF CALIBRATION TECHNIQUES OF AG/AGCL ELECTRODE BETWEEN THE ELECTRICAL CONDUCTIVITY AND THE SPECTRAL ACTIVE TECHNIQUES

机译:电导率和光谱活性技术对AG / AGCL电极标定技术的比较

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Two creative techniques were developed to correct the potential of an Ag/AgCl reference electrode for ensuring the long-term performance in very dilute solutions. For the electrode correction, we used the changes of the electrical conductivity and the UV/VIS absorbance of the internal electrolyte, respectively. The electrical conductivity increased linearly with an increase of the KC1 concentration, with a logarithmic scale. The UV/VIS absorbance of the KC1 solution added with triphenylmethane (TPMe) was observed to be quite linear with an increase in the TPMe concentration. The potential shift decreased linearly with an increase in the KC1 concentration, with a logarithmic scale. From these results, two different linear relationships were obtained. The first relationship was between the electrical conductivity of the internal electrolyte and the potential shift of the Ag/AgCl electrode. The second was a relationship between the UV/VIS absorbance of the internal electrolyte and the potential shift. For simulating a long-term exposure of the electrode, an Ag/AgCl electrode was treated with a tiny perforation as a junction. During the dilution of the internal electrolyte of the Ag/AgCl electrode, the diluted concentration of the internal electrolyte was estimated by using the electrical conductivity and the UV/VIS absorbance, respectively. In view of the good agreement between the estimated and measured potential values, the feasibility of the suggested calibration techniques was confirmed.
机译:开发了两种创造性技术以校正AG / AGCl参比电极的电位,以确保在非常稀释的溶液中的长期性能。对于电极校正,我们使用电导率的变化和内部电解质的UV / Vis吸光度。电导率随着KC1浓度的增加而线性增加,具有对数标度。随着TPME浓度的增加,观察到用三苯基甲烷(TPME)添加的KC1溶液的UV / Vis吸收率是非常线性的。电位偏移随着KC1浓度的增加而导入线性降低,具有对数标度。从这些结果中,获得了两种不同的线性关系。第一关系是在内部电解质的电导率和Ag / AgCl电极的电位偏移之间。第二个是内部电解质的UV / VIS吸光度与电位变化之间的关系。为了模拟电极的长期曝光,将Ag / AgCl电极用微小穿孔处理,作为结。在稀释Ag / AgCl电极的内部电解质期间,通过使用电导率和UV / VIS吸光度估计内电解质的稀释浓度。鉴于估计和测量潜在值之间的良好一致性,确认了建议的校准技术的可行性。

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