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首页> 外文期刊>Electrochimica Acta >Electrochemically induced chemical sensor properties in graphite screen-printed electrodes: The case of a chemical sensor for uranium
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Electrochemically induced chemical sensor properties in graphite screen-printed electrodes: The case of a chemical sensor for uranium

机译:石墨丝网印刷电极中的电化学感应化学传感器特性:铀化学传感器的情况

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摘要

We report for the first time on the possibility to develop chemical sensors based on electrochemically treated, non-modified, graphite screen-printed electrodes (SPEs). The applied galvanostatic treatment (5 μA for 6 min in 0.1 M H_2SO_4) is demonstrated to be effective for the development of chemical sensors for the determination of uranium in aqueous solutions. A detailed study of the effect of various parameters related to the fabrication of SPEs on the performance of the resulting sensors along with some diagnostic experiments on conventional graphite electrodes showed that the inducible analytical characteristics are due to a synergy between electrochemical treatment and ink's solvents. Indeed, the amount of the latter onto the printed working layer controls the achievable sensitivity. The preconcentration of the analyte was performed in an electroless mode in an aqueous solutions of U(VI), pH 4.6, and then, the accumulated species was reduced by means of a differential pulse voltammetry scan in 0.1 M H_3BO_3, pH 3. Under selected experimental conditions, a linear calibration curve over the range 5 × 10~(-9) to 10~(-7) M U(VI) was constructed. The 3σ limit of detection at a preconcentration time of 30 min, and the relative standard deviation of the method were 4.5 × 10~(-9) M U(VI) and >12% (n = 5,5 × 10~(-8) M U(VI)), respectively. The effect of potential interferences was also examined.
机译:我们首次报告了基于电化学处理的非改性石墨丝网印刷电极(SPEs)开发化学传感器的可能性。所应用的恒电流处理(在0.1 M H_2SO_4中5μA持续6分钟)被证明对于开发用于测定水溶液中铀的化学传感器是有效的。对与SPE制备相关的各种参数对所得传感器性能的影响进行的详细研究,以及对常规石墨电极的一些诊断实验表明,可诱导的分析特性归因于电化学处理与油墨溶剂之间的协同作用。实际上,后者在印刷工作层上的量控制了可达到的灵敏度。分析物的预浓缩是在pH 4.6的U(VI)水溶液中以化学方式进行的,然后通过差分脉冲伏安扫描在pH 3的0.1 M H_3BO_3中减少累积的物质。在5×10〜(-9)至10〜(-7)MU(VI)范围内建立了线性校正曲线。预浓缩30分钟时的3σ检出限以及该方法的相对标准偏差为4.5×10〜(-9)MU(VI)和> 12%(n = 5,5×10〜(-8) )MU(VI))。还检查了潜在干扰的影响。

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