Construction of all-solid-state ion-selective sensors using electrolyte-containing polymers.

IF 1.8 4区 化学 Q3 CHEMISTRY, ANALYTICAL Analytical Sciences Pub Date : 2024-10-17 DOI:10.1007/s44211-024-00678-5
Hiroki Ohashi, Keisei Sowa, Yuki Kitazumi, Osamu Shirai
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Abstract

All-solid-state NO3-, K+, NH4+, Na+, and Ca2+ ion-selective sensors (ISEs) were prepared using polyvinyl butyral (S-LEC®K KX-5). In the present case, polyvinyl butyral was used as a porous material to keep the internal solution of the respective ISE. All sensors exhibited near-Nernst responses in the concentration region between approximately 10-5 and 0.1 mol dm-3. To avoid the influence of KCl as interfering ions, MgSO4 was used as an electrolyte within the salt bridge. Although the liquid junction potential was generated, the potential difference was stabilized within about few minutes. The NO3--ISE showed high stability with no potential drift during 12 h of continuous measurements and maintained high sensitivity even after 3 weeks of storage in ultrapure water. Solidification of the internal solution is expected to make the sensor smaller and increase its mechanical strength. As an actual measurement, the sodium concentration in plasma samples using the Na+-ISE was measured to confirm agreement with literature values.

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利用含电解质聚合物构建全固态离子选择性传感器。
使用聚乙烯醇缩丁醛(S-LEC®K KX-5)制备了全固态 NO3-、K+、NH4+、Na+ 和 Ca2+ 离子选择性传感器(ISE)。在这种情况下,聚乙烯醇缩丁醛被用作多孔材料,以保持相应 ISE 的内部溶液。在约 10-5 至 0.1 mol dm-3 的浓度范围内,所有传感器都表现出接近于 Nernst 的响应。为了避免 KCl 作为干扰离子的影响,盐桥内使用了 MgSO4 作为电解质。虽然产生了液结电位,但电位差在几分钟内就趋于稳定。NO3--ISE 显示出很高的稳定性,在 12 小时的连续测量中没有电位漂移,即使在超纯水中存放 3 周后仍能保持很高的灵敏度。内部溶液的凝固预计会使传感器变小并增加其机械强度。在实际测量中,使用 Na+-ISE 测量了血浆样本中的钠浓度,证实与文献值一致。
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来源期刊
Analytical Sciences
Analytical Sciences 化学-分析化学
CiteScore
2.90
自引率
18.80%
发文量
232
审稿时长
1 months
期刊介绍: Analytical Sciences is an international journal published monthly by The Japan Society for Analytical Chemistry. The journal publishes papers on all aspects of the theory and practice of analytical sciences, including fundamental and applied, inorganic and organic, wet chemical and instrumental methods. This publication is supported in part by the Grant-in-Aid for Publication of Scientific Research Result of the Japanese Ministry of Education, Culture, Sports, Science and Technology.
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