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A New N-Heterocyclic Carbene Ionophore in Plasticizer-free Polypyrrole Membrane for Determining Ag+ in Tap Water

机译:无增塑剂聚吡咯膜中的一种新型N-杂环碳环离子体测定自来水中的Ag +

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A bis[1-benzyl-benzimidazoliumethyl]-4-methylbenzenesufonamide bromide ligand (NHCL) as a new type of ionophore was successfully synthesized for the first time and used for the fabrication of Ag+ ion selective electrode as a new type of ionophore, based on the self-plasticizing method. The ionophore was characterized using CHN elemental analysis, FT-IR, H-1 NMR, C-13 NMR, UV-vis spectroscopic techniques and X-ray single crystal diffraction. The interection between NHCL and Ag+ cation was studied spectrophotometerically and the stoichiometry of the complex (1: 2) NHCL: Ag+ in DMSO solvent was determined. The potentiometric response of the electrode toward Ag+ cation was linear from 2.5 x 10(-6) to 1.0 x 10(-1) M with detection limit of 2.00 x 10(-6) M and a Nernstian slope of 58.48 +/- 0.75 mV decade(-1). The sensor exhibited a response time of about 20 seconds at room temperature and working pH range between 3.5-9.0. The electrode showed a good selectivity towards Ag+ cations in comparison with other soft and hard metals, while most of these metal ions did not show significant interference (K-Ag+,M(pot)). The proposed electrode also applied in the direct determination of Ag+ cations in tap water and standard samples with sensible accuracy and precision. (C) 2016 Elsevier Ltd. All rights reserved.
机译:首次成功合成了作为新型离子载体的双[1-苄基苯并咪唑鎓乙基] -4-甲基苯磺酰氨基溴化物配体(NHCL),并在此基础上将其用于制备作为新型离子载体的Ag +离子选择性电极。自塑化方法。使用CHN元素分析,FT-IR,H-1 NMR,C-13 NMR,UV-可见光谱技术和X射线单晶衍射对离子载体进行表征。用分光光度计研究了NHCL和Ag +阳离子之间的相互作用,并确定了DMCL溶剂中NHCL:Ag +(1:2)配合物的化学计量。电极对Ag +阳离子的电位响应从2.5 x 10(-6)到1.0 x 10(-1)M呈线性,检测极限为2.00 x 10(-6)M,Nernstian斜率为58.48 +/- 0.75 mV十年(-1)。该传感器在室温和3.5-9.0的工作pH范围内显示约20秒的响应时间。与其他软金属和硬金属相比,该电极对Ag +阳离子具有良好的选择性,而这些金属离子中的大多数都没有表现出明显的干扰(K-Ag +,M(pot))。拟议的电极还用于灵敏的准确度和精确度的直接测定自来水和标准样品中的Ag +阳离子。 (C)2016 Elsevier Ltd.保留所有权利。

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