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首页> 外文期刊>Electroanalysis >Electrochemical Kinetics of Anodic Ni Dissolution in Aqueous Media as a Function of Chloride Ion Concentration at pH Values Close to Physiological Conditions
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Electrochemical Kinetics of Anodic Ni Dissolution in Aqueous Media as a Function of Chloride Ion Concentration at pH Values Close to Physiological Conditions

机译:pH值接近生理条件时,阳极镍在水介质中溶解的电化学动力学随氯离子浓度的变化

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We have studied the electrochemical kinetics of anodic Ni dissolution as a function of chloride ion concentration, at pH5, 6 and 7, in order to mimic the conditions of sweat samples. Our results show that the rate-determining step for Ni dissolution in the mentioned pH range is the transfer of one first electron, as suggested by the Tafel slopes close to 0.120V/decade. However, the reaction order in chloride ion varies from ca. 2 at pH7 to values close to unity for pH values between 5 and 6. This finding is very important for sensor applications in sweat fluids since the sensitivity of the Ni electrode to chloride ions is higher in neutral solutions (pH ca. 7) compared to that in slightly acid solutions (pH between 5 and 6). Small variations in pH in real samples are expected so this change in sensitivity should be considered when sensing chloride ions in sweat fluids.
机译:为了模拟汗液样品的条件,我们研究了在pH5、6和7下阳极Ni溶解的电化学动力学与氯离子浓度的关系。我们的结果表明,在上述pH范围内,Ni溶解的决定速率的步骤是一个第一电子的转移,正如Tafel斜率接近0.120V /十倍所表明的。但是,氯离子中的反应顺序为约3。在pH7时,pH值从2变为接近于5到6的统一值。这一发现对于汗液中的传感器应用非常重要,因为与中性溶液(pH约为7)相比,Ni电极对氯离子的灵敏度更高。在弱酸性溶液中(pH在5到6之间)。预计实际样品中的pH会有很小的变化,因此在检测汗液中的氯离子时,应考虑灵敏度的这种变化。

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