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On direct internal methane steam reforming kinetics in operating solid oxide fuel cells with nickel-ceria anodes

机译:带有镍-二氧化铈阳极的固体氧化物燃料电池中直接内部甲烷蒸汽重整动力学的研究

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Major operating challenges remain to safely operate methane fuelled solid oxide fuel cells due to undesirable temperature gradients across the porous anode and carbon deposition. This article presents an experimental study on methane steam reforming (MSR) global kinetics for single operating SOFCs with Ni-GDC (gadolinium doped ceria) anodes for low steam to carbon (S/C) ratios and moderate current densities. The study points out the hitherto insufficient research on MSR global and intrinsic kinetics for operating SOFCs with complete Ni-ceria anodes. Further, it emphasizes the need to develop readily applicable global kinetic models as a subsequent step from previously reported state-of-art and complex intrinsic models. Two rate expressions of the Power law (PL) and Langmuir-Hinshelwood (LH) type have been compared and based on the analysis, limitations of using previously proposed rate expressions for Ni catalytic beds to study MSR kinetics for complete cermet anodes have been identified. Firstly, it has been shown that methane reforming on metallic (Ni) current collectors may not be always negligible, contrary to literature reports. Both PL and LH kinetic models predict significantly different local MSR reaction rate and species partial pressure distributions along the normalized reactor length, indicating a strong need for further experimental verifications. (C) 2017 Elsevier B.V. All rights reserved.
机译:由于横跨多孔阳极的不期望的温度梯度和碳沉积,安全操作以甲烷为燃料的固体氧化物燃料电池仍然是主要的操作挑战。本文介绍了使用Ni-GDC(ga掺杂二氧化铈)阳极的单操作SOFC的甲烷蒸汽重整(MSR)整体动力学的实验研究,以降低蒸汽/碳(S / C)比和适中的电流密度。研究指出,迄今为止,对于使用完整的二氧化铈阳极的SOFC的MSR全局和内在动力学研究还不够。此外,它强调需要从先前报道的最新技术和复杂的内在模型中发展出易于应用的全局动力学模型作为后续步骤。比较了幂律(PL)和Langmuir-Hinshelwood(LH)类型的两种速率表达式,并基于分析,发现了使用先前提出的Ni催化床速率表达式来研究完整金属陶瓷阳极MSR动力学的局限性。首先,与文献报道相反,已经表明在金属(Ni)集流体上的甲烷重整可能并不总是可以忽略的。 PL和LH动力学模型都预测沿归一化反应堆长度的局部MSR反应速率和物种分压分布存在显着差异,这表明强烈需要进一步的实验验证。 (C)2017 Elsevier B.V.保留所有权利。

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