首页> 外文会议>Conference in Series of the European Fuel Cell Forum in Lucerne;European sofc and soe forum >Experimental clarification of the R.W.G.S. reaction effect in H2O/CO2 SOEC co-electrolysis conditions
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Experimental clarification of the R.W.G.S. reaction effect in H2O/CO2 SOEC co-electrolysis conditions

机译:R.W.S.S.的实验澄清 H2O / CO2 SOEC中的反应效果合同电解条件

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High temperature co-electrolysis of steam/CO2 mixtures using Solid Oxide Cells has been proposed as a promising technology to produce synthesis gas (H2 + CO) which can be processed further towards synthetic hydrocarbon fuels production. Co-electrolysis is a significantly more complicated process than steam electrolysis, because three reactions take place simultaneously; namely H2O electrolysis, CO2 electrolysis and the catalytic Reverse Water Gas Shift reaction (RWGS). Specifically, there are discrepancies whether CO is produced via the RWGS solely and that no electrolysis of CO2 occurs, or if CO is produced both via the RWGS and via electrolysis of CO2. As a result, it is crucial to quantify the degree of CO production for each reaction. In the presented investigation modified X-Ni/GDC electrodes (where X = Au, Mo and Fe) are studied, in the form of half-electrolyte supported cells, for their performance in the RWGS through catalytic-kinetic measurements. The samples were tested at open circuit potential conditions in order to elucidate their catalytic activity towards the production of CO (r_(co)), which is one of the products of the H2O/CO2 co-electrolysis reaction. In brief, it was found that the rate of the produced CO (r_(co)) increases by increasing the operating temperature and the partial pressure of H2 in the reaction mixture. In addition, the first results revealed that Fe-modification enhances the catalytic production of CO, since a 2wt.%Fe-Ni/GDC electrode proved to perform better, compared to all other modified electrodes and Ni/GDC, in the whole studied temperature range (800-900 °C) and for all studied reaction mixtures. The electrocatalytic investigation on electrolyte-supported cells is currently in progress.
机译:已经提出了使用固体氧化物细胞的高温Co-Incoolate使用固体氧化物电池作为产生合成气体(H2 + CO)的有希望的技术,该技术可以进一步加工为合成烃燃料生产。共电解是一种比蒸汽电解更复杂的过程,因为三种反应同时发生;即H 2 O电解,CO2电解和催化反转水换水反应(RWG)。具体地,差异是否仅通过RWGS产生CO,并且不会发生CO 2的电解,或者如果通过RWG和通过CO 2的电解产生CO。结果,量化每种反应的CO生产程度至关重要。在所提出的研究中,通过催化 - 动力学测量,在半电解质支持的细胞的形式中研究改性修饰的X-Ni / GDC电极(其中X = Au,Mo和Fe),通过催化动力学测量在RWG中进行性能。在开放电路电位条件下测试样品,以阐明其朝向CO(R_(CO))的催化活性,这是H 2 O / CO 2共电解反应之一。简而言之,发现所生产的CO(R_(CO))的速率通过增加反应混合物中的工作温度和H 2的分压而增加。此外,第一个结果表明,与所有其他改性电极和Ni / GDC相比,Fe-Deperation的催化作用增强了CO的催化作用。范围(800-900°C)和所有研究的反应混合物。目前正在进行电解质支持的细胞的电催化调查。

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