首页> 外文期刊>Analytical chemistry >Alkalinization of Thin Layer Samples with a Selective Proton Sink Membrane Electrode for Detecting Carbonate by Carbonate-Selective Electrodes
【24h】

Alkalinization of Thin Layer Samples with a Selective Proton Sink Membrane Electrode for Detecting Carbonate by Carbonate-Selective Electrodes

机译:碳酸盐选择性电极通过选择性质子吸收膜电极对薄层样品进行碱化处理

获取原文
获取原文并翻译 | 示例
       

摘要

Potentiometry is known to be sensitive to so-called free ion activity and is a potentially valuable tool in environmental speciation analysis. Here, the direct detection of free and total carbonate is demonstrated by alkalinization of a thin layer sample (similar to 100 mu m), which is electrochemically triggered at a pH responsive membrane placed opposite a carbonate-selective membrane electrode. The concept may serve as a promising future methodology for in situ environmental sensing applications where traditional sampling and pretreatment steps are no longer required. The possibility of increasing the pH of the sample was demonstrated first with a proton selective membrane (pH readout at zero current) placed opposite the thin layer gap. An optimal applied potential (600 mV) for 300 s resulted in a pH increase of 4 units in an artificial sample, with a relative standard deviation (RSD) of similar to 2%. The pH probe was subsequently replaced by a solid contact carbonate selective electrode for the determination of carbonate species (4.17 mu M) in a sample of 1 mM NaHCO3. Increasing the pH to 12.1 by the electrochemically controlled proton sink allowed one to convert bicarbonate to the detectable carbonate species. Initial bicarbonate concentration (similar to 1 mM) was obtained as the difference between the converted bicarbonate and the initial carbonate concentration. An initial application of this concept was illustrated by the speciation analysis of an unfiltered sample from the Arve river (12.3 +/- 0.2 mu M and 22.5 +/- 0.3 mM carbonate and bicarbonate, respectively). The values were confirmed by volumetric titration.
机译:电位计已知对所谓的自由离子活性敏感,并且在环境形态分析中是潜在有价值的工具。在这里,游离和总碳酸盐的直接检测通过薄层样品(类似于100微米)的碱化来证明,这是在与碳酸盐选择性膜电极相对的pH响应膜上通过电化学触发的。对于不再需要传统采样和预处理步骤的原位环境传感应用,该概念可能会成为有希望的未来方法。首先通过与薄层间隙相对放置的质子选择性膜(零电流下的pH读数)证明了增加样品pH值的可能性。持续300 s的最佳施加电势(600 mV)导致人工样品的pH值增加4个单位,相对标准偏差(RSD)接近2%。随后用固体接触式碳酸盐选择电极代替pH探针,以测定1 mM NaHCO3样品中的碳酸盐种类(4.17μM)。通过电化学控制的质子槽将pH值提高到12.1,可以将碳酸氢盐转化为可检测的碳酸盐。获得了原始碳酸氢盐浓度(类似于1 mM)作为转化后的碳酸氢盐和初始碳酸盐浓度之间的差。该概念的最初应用是通过对Arve河中未过滤样品(分别为碳酸盐和碳酸氢盐12.3 +/- 0.2μM和22.5 +/- 0.3 mM)的形态分析说明的。该值通过体积滴定确认。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号