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Enhancing co-production of H2 and syngas via water splitting and POM on surface-modified oxygen permeable membranes

机译:加强氢气的联合生产 表面改性的透氧膜上通过水分解和POM合成和合成气

摘要

In this article, we report a detailed study on co-production of H2 and syngas on La0.9Ca0.1FeO3−δ (LCF-91) membranes via water splitting and partial oxidation of methane, respectively. A permeation model shows that the surface reaction on the sweep side is the rate limiting step for this process on a 0.9 mm-thick dense membrane at 990°C. Hence, sweep side surface modifications such as adding a porous layer and nickel catalysts were applied; the hydrogen production rate from water thermolysis is enhanced by two orders of magnitude to 0.37 μmol/cm2•s compared with the results on the unmodified membrane. At the sweep side exit, syngas (H2/CO = 2) is produced and negligible solid carbon is found. Yet near the membrane surface on the sweep side, methane can decompose into solid carbon and hydrogen at the surface, or it may be oxidized into CO and CO2, depending on the oxygen permeation flux.
机译:在本文中,我们报告了关于La0.9Ca0.1FeO3-δ(LCF-91)膜上分别通过水分解和甲烷部分氧化共同生产H2和合成气的详细研究。渗透模型表明,在990°C厚0.9 mm的致密膜上,吹扫侧的表面反应是该过程的速率限制步骤。因此,进行了扫掠侧表面改性,例如添加多孔层和镍催化剂。与未改性膜的结果相比,水热解制氢的速率提高了两个数量级,达到0.37μmol/ cm2•s。在吹扫侧出口产生了合成气(H2 / CO3 = 2),并且发现的固体碳可以忽略不计。然而,在靠近吹扫侧的膜表面附近,根据氧气的渗透通量,甲烷可以在表面分解为固体碳和氢,或者可以被氧化为CO和CO2。

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