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首页> 外文期刊>Oxidation of Metals >Mechanisms of Oxide Scale Formation on Ferritic Interconnect Steel in Simulated Low and High pO_2 Service Environments of Solid Oxide Fuel Cells
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Mechanisms of Oxide Scale Formation on Ferritic Interconnect Steel in Simulated Low and High pO_2 Service Environments of Solid Oxide Fuel Cells

机译:在固体氧化物燃料电池的低和高pO_2使用环境中,铁素体互连钢上氧化皮形成的机理

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The Laves phase strengthened ferritic steel Crofer 22 H has recently been proposed as construction material for interconnects in solid oxide fuel cells (SOFCs). In the present study, the oxidation kinetics of Crofer 22 H at 800 °C was compared with that of a Mn-free batch during exposure in air and Ar-H_2-H_2O, the latter simulating the anode gas of a SOFC. Main emphasis was put on studying the oxidation mechanisms of Crofer 22 H during the early stages of isothermal reaction as well as during long-term discontinuous exposure. Differences in oxidation mechanisms in air and simulated anode gas (SAG) were denned. Oxidation rates for Crofer 22 H in air were found to be initially slower than in SAG, but the opposite effect was observed after longer exposure times. This effect of atmosphere composition on the oxidation rate is shown to be governed by the time dependent extent to which the inner chromia scale layer is covered by an outer Cr/Mn spinel layer. In both test gases the minor addition of silicon to Crofer 22 H resulted in internal silica formation during the very early stages of oxidation; this effect vanished after longer exposure times. Incorporation of titanium in the scale differed for the two test atmospheres because the oxygen partial pressure affects titanium solubility in chromia and especially the spinel phase.
机译:Laves相增强的铁素体钢Crofer 22 H最近被提出作为固体氧化物燃料电池(SOFC)中互连的建筑材料。在本研究中,将Crofer 22 H在800°C的氧化动力学与无锰批次在空气和Ar-H_2-H_2O暴露期间的氧化动力学进行了比较,后者模拟了SOFC的阳极气体。主要重点放在研究等温反应早期以及长期不连续暴露期间Crofer 22 H的氧化机理。空气和模拟阳极气体(SAG)的氧化机理存在差异。最初发现Crofer 22 H在空气中的氧化速率比SAG中的氧化速率慢,但在更长的暴露时间后观察到相反的效果。气氛组成对氧化速率的影响被显示为由时间决定的程度,内部氧化铬皮层被外部Cr / Mn尖晶石层覆盖。在两种测试气体中,向Crofer 22 H少量添加硅都会在氧化的非常早期阶段形成内部二氧化硅。更长的曝光时间后,这种效果消失了。在两种测试气氛中,钛的掺入量有所不同,因为氧分压会影响氧化铬(尤其是尖晶石相)中钛的溶解度。

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