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ENZYME GAS-DIFFUSION ELECTRODES ― MATHEMATICAL MODELLING

机译:酶气体扩散电极 - 数学建模

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摘要

A mathematical model of an enzyme-gas diffusion electrode for detection of phenol in solution described previously is used. Two step enzymatic reaction turns the phenol consecutively to catehol (stage 1) and to o-quinone (stage 2), the latter being converted by the electrochemical indicator electrode reaction back to catehol which can be looped again in the stage 2 of the enzymatic reaction; this can result in an internal gain of the am-perometric signal. The system of partial differential equations is solved numerically for discrete moments of time and spatial distributions of the concentrations of phenol, catechol and o-quinone into the membrane and the enzyme layers are obtained, as well as the current of the electrode. From the values of the steady-state current, a calibration curve, which shows good correlation with experimental data, is built. The concentration profiles of the species involved, as well as the spatial distribution in the layers of the rate of the enzyme reactions obtained at different moments of time are compared for two significantly different values of the initial concentration of phenol in the solution. It is shown that loop of the product of the indicator reaction again in the enzymatic reaction makes the electrode more sensitive to lower phenol concentrations in the bulk solution.
机译:使用用于检测先前描述的溶液中酚类气体扩散电极的数学模型。两步酶反应将苯酚连续转向Catehol(阶段1)和O-醌(第2阶段),后者被电化学指示器电极反应转换回凯霍尔,这可以在酶反应的第2层中再次环绕;这可能导致AM-remolign信号的内部增益。数差分方程的系统在数值上进行了解决,用于离散的时间和酚,儿茶酚和O-醌进入膜的浓度的空间分布,并获得酶层,以及电极的电流。从稳态电流的值,建立了校准曲线,其显示与实验数据良好相关的校准曲线。将所涉及的物种的浓度分布以及在不同时刻获得的酶反应速率的层中的空间分布进行比较,在溶液中初始苯酚的初始浓度的两个显着不同的值。结果表明,在酶促反应中再次进行指示剂反应的产物的环,使电极对散装溶液中的较低酚浓度更敏感。

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