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Higher Harmonic Large-Amplitude Fourier Transformed Alternating Current Voltammetry: Analytical Attributes Derived from Studies of the Oxidation of Ferrocenemethanol and Uric Acid at a Glassy Carbon Electrode

机译:高次谐波大振幅傅立叶变换交流伏安法:分析属性源自玻璃碳电极上二茂铁甲醇和尿酸的氧化研究

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An analytical evaluation of the higher ac harmonic components derived from large amplitude Fourier transformed voltammetry is provided for the reversible oxidation of ferrocenemethanol (FcMeOH) and oxidation of uric acid by an EEC mechanism in a pH 7.4 phosphate buffer at a glassy carbon (GC) electrode. The small background current in the analytically optimal fifth harmonic is predominantly attributed to faradaic current associated with the presence of electroactive functional groups on the GC electrode surface, rather than to capacitive current which dominates the background in the dc, and the initial three ac harmonics. The detection limits for the dc and the first to fifth harmonic ac components are 1.9, 5.89, 2.1, 2.5, 0.8, and 0.5 (mu)M for FcMeOH, respectively, using a sine wave modulation of 100 mV at 21.46 Hz and a dc sweep rate of 111.76 mV s~(-1). Analytical performance then progressively deteriorates in the sixth and higher harmonics. For the determination of uric acid, the capacitive background current was enhanced and the reproducibility lowered by the presence of surface active uric acid, but the rapid overall 2e~(-) rather than 1e~(-) electron transfer process gives rise to a significantly enhanced fifth harmonic faradaic current which enabled a detection limit of 0.3 (mu)M to be achieved which is similar to that reported using chemically modified electrodes. Resolution of overlapping voltammetric signals for a mixture of uric acid and dopamine is also achieved using higher fourth or fifth harmonic components, under very low background current conditions. The use of higher fourth and fifth harmonics exhibiting highly favorable faradaic to background (noise) current ratios should therefore be considered in analytical applications under circumstances where the electron transfer rate is fast.
机译:对大振幅傅立叶变换伏安法得出的较高交流谐波分量的分析评估,用于在玻璃碳(GC)电极的pH 7.4磷酸盐缓冲液中通过EEC机理进行二茂铁甲醇(FcMeOH)的可逆氧化和尿酸的氧化。 。在分析上最佳的五次谐波中,较小的背景电流主要归因于与GC电极表面上存在电活性官能团有关的法拉第电流,而不是归因于主导直流中本底的电容性电流以及最初的三个ac谐波。使用100 mV在21.46 Hz的正弦波调制和dc,对于FcMeOH,dc和第一至第五谐波ac分量的检测极限分别为1.9、5.89、2.1、2.5、0.8和0.5μM扫描速率为111.76 mV s〜(-1)。然后,在六次或更高次谐波中,分析性能会逐渐降低。对于尿酸的测定,由于存在表面活性尿酸,电容性本底电流得到增强,可重复性降低,但是快速的整体2e〜(-)而不是1e〜(-)电子转移过程显着增加了增强的五次谐波法拉第电流,能够实现0.3μM的检出限,这与使用化学修饰电极报告的检出限相似。在非常低的背景电流条件下,使用较高的四阶或五阶谐波分量也可以解决尿酸和多巴胺混合物的重叠伏安信号。因此,在电子传输速度快的情况下的分析应用中,应考虑使用表现出非常有利的法拉第与背景(噪声)电流比的较高的第四和第五谐波。

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