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A study of the electrochemical oxidation of hydrogen peroxide on a platinum rotating disk electrode in the presence of calcium ions using Michaelis-Menten kinetics and binding isotherm analysis

机译:利用Michaelis-Menten动力学和结合等温线分析研究钙离子存在下铂旋转盘电极上过氧化氢的电化学氧化

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The present work demonstrates a potential suppression in the electrochemical signal of H{sub}2O{sub}2 oxidation due to the presence of Ca{sup}(2+) ions. A mechanistic scheme was proposed to include a reversible interaction of Ca{sup}(2+) ions with either the electrode surface binding sites (competitive) or the complex sites (non-competitive). The degree of inhibition was inspected by evaluating the kinetic currents as a function of [Ca{sup}(2+)] applying Koutecky-Levich kinetics. These observations were further supported with models based on enzyme kinetics such as Michaelis-Menten model applying Lineweaver-Burk plot along with non-linear least-square fitting analysis. The experimental results suggests that the strength of the complex binding sites decreases considerably with increasing [Ca{sup}(2+)] and that a single H{sub}2O{sub}2 molecule is required to combine with one available active binding site.
机译:本工作证明了由于Ca {sup}(2+)离子的存在,H {sub} 2O {sub} 2氧化的电化学信号受到了抑制。提出了一种机制方案,包括Ca {sup}(2+)离子与电极表面结合位点(竞争性)或复杂位点(非竞争性)的可逆相互作用。通过应用Koutecky-Levich动力学评估作为[Ca {sup}(2+)]的函数的动电流来检查抑制程度。这些观察结果得到了基于酶动力学的模型的进一步支持,例如使用Lineweaver-Burk图以及非线性最小二乘拟合分析的Michaelis-Menten模型。实验结果表明,复杂的结合位点的强度随着[Ca {sup}(2+)]的增加而显着降低,并且需要单个H {sub} 2O {sub} 2分子与一个可用的活性结合位点结合。

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