铂化聚2,5-二甲氧基苯胺电极的实验研究

Lizong Dai , Jean-Yves Gal , Huihuang Wu
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引用次数: 2

摘要

在化学催化和分析化学领域,通过沉积多层材料修饰金属电极是在20年前发展起来的。我们工作的目的是比较用取代聚苯胺制备的电极与分析化学中常用的电极:铂、铂化铂和玻璃碳的行为。我们首先介绍了聚2,5-二甲氧基苯胺(PDMAn)在两个经典体系上的结果:Fe(CN)63 - /Fe(CN)64 -和O2/OH -对。第一个例子在电化学训练中经常被研究,因为通常得到了很好的结果。Levich方程得到了有效的验证。另一方面,氧的还原和OH -离子的氧化总是受到电子转移反应速率的限制。在我们看来,研究这两种体系在铂电极上覆盖PDMAn的行为,无论是否镀铂,都可能是有趣的。研究了异丙醇在弱酸介质中的氧化反应。在分析化学领域,在决定使用取代聚苯胺薄膜修饰电极的可能性之前,必须进行更详细的研究。不镀铂的电极似乎是没有用的;将铂化聚合物沉积在比铂更便宜的衬底(例如玻碳)上制备电极可能会更有趣。在较宽的电位范围内形成H2O2将是氧化的最佳结果,并将进行新的实验研究。
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Experimental study of platinized poly-2,5-dimethoxyaniline electrodes

In the domains of chemical catalysis and analytical chemistry, the modification of metal electrodes by the deposition of multilayers was developed about twenty years ago. The purpose of our work was to compare the behavior of an electrode prepared with a substituted polyaniline with that of electrodes regularly used in analytical chemistry: platinum, platinized platinum and glassy carbon. We initially present results obtained with poly-2,5-dimethoxyaniline (PDMAn) on two classic systems: the couple Fe(CN)63–/Fe(CN)64– and the couple O2/OH. The first example is often studied during training in electrochemistry because of the good results generally obtained. Levich’s equation is effectively well verified. On the other hand, reduction of oxygen and oxidation of OH ions are always limited by the rate of the electron transfer reactions. It seems to us that the study of the behavior of these two systems with platinum electrodes covered with PDMAn, platinized or not, could be interesting. The oxidation of isopropanol in a weakly acid medium was also investigated. In the field of analytical chemistry, a more detailed study is mandatory before deciding on the possibility of using electrodes modified with films of substituted polyaniline. An electrode, which would not be platinized, does not seem useful; the use of electrodes prepared with platinized polymers deposited on substrates less expensive than platinum, (glassy carbon for example), may be more interesting. It seems that H2O2 formation over a wide domain of potential would be the best result for oxidations and new experiments will be investigated.

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