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使用选择性质子吸收膜电极对薄层样品进行碱化,以便通过碳酸盐选择性电极检测碳酸盐。

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

作者信息

Jansod Sutida, Ghahraman Afshar Majid, Crespo Gastón A, Bakker Eric

机构信息

Department of Inorganic and Analytical Chemistry, University of Geneva , Quai Ernest-Ansermet 30, CH-1211 Geneva, Switzerland.

出版信息

Anal Chem. 2016 Apr 5;88(7):3444-8. doi: 10.1021/acs.analchem.6b00346. Epub 2016 Mar 16.

Abstract

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 (∼100 μm), 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 ∼2%. The pH probe was subsequently replaced by a solid contact carbonate selective electrode for the determination of carbonate species (4.17 μM) 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 (∼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 μM and 22.5 ± 0.3 mM carbonate and bicarbonate, respectively). The values were confirmed by volumetric titration.

摘要

电位分析法对所谓的自由离子活性很敏感,是环境形态分析中一种潜在的有价值工具。在此,通过对薄层样品(约100μm)进行碱化来直接检测游离和总碳酸盐,该碱化过程在与碳酸盐选择性膜电极相对的pH响应膜处通过电化学触发。这一概念可能成为未来原位环境传感应用的一种有前景的方法,在此类应用中不再需要传统的采样和预处理步骤。首先,通过在薄层间隙对面放置质子选择性膜(零电流下读取pH值)证明了提高样品pH值的可能性。在人工样品中,施加600mV的最佳电位300s导致pH值增加4个单位,相对标准偏差(RSD)约为2%。随后,将pH探针替换为固体接触碳酸盐选择性电极,用于测定1mM NaHCO₃样品中的碳酸盐形态(4.17μM)。通过电化学控制的质子阱将pH值提高到12.1,可以将碳酸氢盐转化为可检测的碳酸盐形态。初始碳酸氢盐浓度(约1mM)通过转化后的碳酸氢盐与初始碳酸盐浓度之差获得。通过对阿尔韦河未过滤样品的形态分析(碳酸盐和碳酸氢盐分别为12.3±0.2μM和22.5±0.3mM)说明了这一概念的初步应用。这些值通过容量滴定得到了证实。

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