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Electrical conductivity of magnetically stabilized fluidized-bed electrodes - Chronoamperometric and impedance studies

机译:磁稳定流化床电极的电导率 - 计时率和阻抗研究

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Fluidized-bed electrodes could offer an interesting way to increase the electrode surface area applicable in electrochemical processes when the problem of poor electrical contact within the particle bed could be overcome. We recently demonstrated, that the contacting can be improved by the use of magnetizable electrode particles and the superposition of a magnetic field. However, details of the magnetic influence on the charge transport are still mostly unknown. In this work, we investigate the electrodynamics of a fluidized bed electrode with and without the superposition of a magnetic field by means of chronoamperometry and electrochemical impedance spectroscopy (EIS). In the chronoamperometric studies two types of charge transfer mechanism can be distinguished by the slope of the resistance increase with increasing distance between the electrodes. In close proximity to the electrodes direct conductive charge transfer along statistically formed particle chains dominates. Because the probability of uninterrupted particle chains quickly diminishes with increasing length, above a certain distance of approx. 6 mm a second, so-called convective, charge transfer mechanism dominates. This mechanism is based on the transfer of electrons between colliding fluidized particles and corresponds with a substantially higher specific resistance. The conductive charge transfer mechanism can be enhanced by up to a factor of four applying a superimposed magnetic field, while the second mechanism shows only a weak field dependence. The presented equivalent circuit model and the magnetic field dependency of its parameters contribute to a deeper understanding of the novel magnetically stabilized fluidized bed electrode and demonstrate the usefulness of EIS measurements for the prediction of the effectiveness of a particle based electrochemical reactor.
机译:当颗粒床内的电接触差的问题克服,流化床电极可以提供一种有趣的方式来增加适用于电化学过程中的电极表面积。我们最近证明,通过使用可磁化电极颗粒和磁场的叠加可以改善接触。然而,对电荷传输的磁性影响的细节仍然大多是未知的。在这项工作中,我们通过计时率和电化学阻抗光谱(EIS)来研究流化床电极的电动力学和不具有磁场的叠加。在计时的研究中,通过电极之间的距离增加,可以通过电阻增加的斜率来区分两种类型的电荷转移机构。沿着电极接近电极直接导电电荷转移沿统计形成的颗粒链占主导地位。因为不间断颗粒链的概率随着长度的增加而快速减少,所以高于一定距离约为约。秒为6毫米,所谓的对流,电荷转移机制占主导地位。该机制基于碰撞流化颗粒之间的电子转移,并且对应于基本上更高的特异性电阻。导电电荷传递机构可以通过高达施加叠加磁场的四倍,而第二机制仅显示弱场依赖性。所呈现的等效电路模型及其参数的磁场依赖性有助于更深入地了解新型磁稳压流化床电极,并证明EIS测量对粒子基电化学反应器的有效性的有用性。

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