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Narrow gap flow electrolysis cells and the challenge of hydrogen bubbles – a combined approach via modelling and experiment

Narrow gap flow electrolysis cells and the challenge of hydrogen bubbles – a combined approach via modelling and experiment
窄间隙流电解池和氢气泡的挑战——建模和实验相结合的方法
批准号:
433305109
负责人:
Professorin Dr. Friederike Schmid
金额:
$0.0万
依托单位:
依托单位国家:
德国
项目类别:
Research Units
财政年份:
2019
资助国家:
德国
项目状态:
已结题
起止时间:
2018-12-31 至 2023-12-31

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中文摘要
翻译
为了以后在技术规模上应用电解转换,电解的施加电压必须低,以确保高能效。解决这个问题的一个概念是在阳极和阴极表面之间使用一个小的距离。人们发现,这样窄的间隙可以使用导电性较低的介质。通常,离子越少,电压降越小。这一点尤其重要,因为由于盐负荷较低,电解质的下游加工得到了简化。在计划中的项目中,建模将用于研究低盐浓度或无盐情况下薄膜的导电性机制。我们将重点关注电场的作用——即使施加的电压很小,电场在薄膜中也会很大——对于介质的分子结构,无论是在体积上还是在靠近电极表面上。此外,我们将研究电场对介质动力学和粘度的影响,以阐明在粘度问题和质量传递对电解产生不利影响之前,这种电池可以变得多薄。研究网络中的第二个挑战是使用流动电解电池时分子氢的形成。这种阴极反应在这种框架内是理想的,但是具有未分裂细胞几何形状的流动电池,由于体积增加,可能被大气泡阻挡。因此,这种电池的效率受到很大的限制。为了控制这一普遍问题,我们采取了两种方法。一方面,要使用支持表面活性剂来限制气泡的大小,并产生至少仍具有导电性并继续支持电解的泡沫。另外,不同的电极布置也将被测试。这一部分也将通过建模研究来支持。另一种方法是在载流子结构上使用非常薄的钯箔来去除阴极后面的氢,而不会影响所需电解的窄间隙。
英文摘要
For a later application of electrolytic conversions on a technical scale, the applied voltage for the electrolysis has to be low to ensure a high energy efficiency. One concept to tackle this is to employ a small distance between anode and cathode surface. Such narrow gaps have been found to allow the use of less conductive media. Usually, fewer ions also induce a smaller voltage drop. This is particularly important, because the downstream processing of the electrolytes is simplified due to a lower salt load. Within the planned project, modeling will be used to investigate the mechanisms of conductivity in thin films at low salt concentration or in the absence of salt. We will focus on the role of the electric field – which can be large in thin films even if the applied voltage is small - for the molecular structure of the medium, both in the bulk and close to the electrode surfaces. Furthermore, we will investigate the effect of electric fields on the dynamics and the viscosity of the medium, in order to elucidate how thin such cells can become before viscosity problems and mass transport adversely affect electrolysis. A second challenge within the research network is the formation of molecular hydrogen when using flow electrolysis cells. This cathodic reaction is desired within this framework, but flow cells with undivided cell geometry, can be blocked by large gas bubbles due to their increased volume. Thus, the efficiency of such cells is greatly limited. Here, two approaches are being pursued in order to get this general problem under control. On the one hand, supporting surfactants are to be used which limit the size of the gas bubbles and produce at least a foam which is still conductive and continues to support electrolysis. Alternatively, divergent electrode arrangements will be tested as well. This part will also be supported by modeling studies. An alternative way will be to use very thin palladium foils on carrier structures to remove the hydrogen behind the cathode, without affecting narrow gap for the desired electrolysis.
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