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On the methane oxidation activity of Sr_2(MgMo)_2O_(6-δ): a potential anode material for direct hydrocarbon solid oxide fuel cells

机译:Sr_2(MgMo)_2O_(6-δ)的甲烷氧化活性:直接碳氢固体氧化物燃料电池的潜在阳极材料

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摘要

Sr_2(MgMo)_2O_(6-δ) and materials of nominal compositions with increased and decreased Mo content were synthesized and their stability and catalytic activity towards CH_4 oxidation characterized under solid oxide fuel cell (SOFC) anode conditions. Sr_2(MgMo)_2O_(6-δ) was synthesized as a double perovskite. Materials with increased Mo content formed a mixture of the double perovskite Sr_2MgMoO_(6-δ) and the single perovskite SrMoO_3, after synthesis in H_2, with the amount of SrMoO_3 increasing with increasing Mo content. SrMoO_3 is unstable in air and slowly oxidized to the scheelite-structured impurity SrMoO_4. All compositions decomposed to Mo, MgO and SrO in dry 20% CH_4/N_2 at temperatures ≥ 850 ℃. CH_4 reaction rates were catalytically limited with measured rates significantly lower than for La_(0.75)Sr_(0.25)Cr_(0.5)Mn_(0.5)O_(3-δ). Rates increased by 1-2 orders of magnitude when 2 wt-% of Pt was added to the surface.
机译:合成了Sr_2(MgMo)_2O_(6-δ)和钼含量增加和减少的名义组成的材料,并在固体氧化物燃料电池(SOFC)阳极条件下表征了其稳定性和对CH_4氧化的催化活性。 Sr_2(MgMo)_2O_(6-δ)合成为双钙钛矿。 Mo含量增加的材料在H_2中合成后,形成了双重钙钛矿Sr_2MgMoO_(6-δ)和单一钙钛矿SrMoO_3的混合物,随着Mo含量的增加,SrMoO_3的含量增加。 SrMoO_3在空气中不稳定,并缓慢氧化为白钨矿结构杂质SrMoO_4。在干燥的20%CH_4 / N_2中,在≥850℃的温度下,所有成分均分解为Mo,MgO和SrO。 CH_4反应速率受到催化限制,实测速率明显低于La_(0.75)Sr_(0.25)Cr_(0.5)Mn_(0.5)O_(3-δ)。当将2 wt%的Pt添加到表面时,速率增加1-2个数量级。

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