新型pantazene配体修饰碳糊电极的构建用于实际样品中离子银的超痕量测定

M. Payehghadr, Samaneh Salarvand, Farzaneh Nourifard, M. K. Rofouei, N. Bahramipanah
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引用次数: 7

摘要

以4-甲氧基苯胺(对甲氧基苯胺)与乙胺为原料,合成了新的配体1,5-二(对甲氧基苯基)-3-乙基-1,4-pantaazadiene。将混合物在冰浴中搅拌30分钟。合成化合物的结构由IR、1HNMR和13CNMR测定。然后,用该配体修饰了碳糊电极,用于纳摩尔浓度银的测定。在pH=4.8的醋酸缓冲溶液中,采用循环伏安法(CV)和差分脉冲伏安法(DPV)研究了该修饰电极的电化学性能。考察了pH、扫描速率、改性剂和缓冲液作为支撑电解质的比例对电极过程的影响。Ag+在0.4 ~ 0.5 V左右出现氧化峰。所得电极在10-9 ~ 10-8 mol.L-1的银浓度范围内表现出线性响应,检测极限值为1.61×10-10mol。L-1,基于信噪比为3。电极性能相对标准偏差(RSD%)为2.41%。该MCPE对水溶液中Ag+离子具有较高的灵敏度和选择性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Construction of modified carbon paste electrode by a new pantazene ligand for ultra-trace determination of ion silver in real samples
A new ligand, 1,5-bis( para methoxyphenyl)-3- ethyl-1,4-pantaazadiene has been synthesized by reaction of the 4-methoxyaniline (p-anisidine) with ethylamine. The mixture was stirred in an ice bath for 30 min. The structure of the synthesized compound resulted from the IR and 1HNMR and 13CNMR. Afterwards, a carbon paste electrode modified with this new ligand was developed for the silver determination at nanomolar level concentration. The electerochemical properties of this modified electrode was investigated by employing cyclic voltammetry (CV) and differential pulse voltammetry (DPV) methods in an acetate buffer solution (pH=4.8). The effect of pH, scan rate, percentage of modifier and buffer as supporting electrolyte on the electrode process were investigated. The oxidation peak of Ag+ was observed at about 0.4- 0.5 V. The resulting electrode demonstrated linear response across a 10-9 to 10-8 mol.L-1 of silver concentration range with a detection limit value of 1.61×10-10mol.L-1, on the basis of a signal to noise ratio of 3. Relative Standard deviation (RSD%) of the electrode performance was 2.41%. This MCPE, were showed high sensitivity and selectivity to Ag+ ions in aqueous samples.
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