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Novel Anode-Supported Tubular Solid-Oxide Electrolytic Cell for Direct NO Decomposition in N2 Environment

机译:N 2 环境中用于阳极直接分解的新型阳极支撑管状固体氧化物电解槽

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An anode-supported tubular solid-oxide electrolytic cell (AT-SOEC) for NO decomposition has beendesigned and fabricated successfully by dip-coating technique. The AT-SOEC comprised porous(La0.8Sr0.2)0.95MnO3 (LSM95) as anode substrate, LSM95/8 mol% yttria stabilized zirconia (8YSZ) asboth anode active layer and cathode layer, and 8YSZ as electrolyte. XRD patterns demonstrated thatLSM95 and 8YSZ had good phase stability at 1250 C and in NO atmosphere which indicated thatthey were proper electrode and electrolyte materials for NO decomposition. Electrodes with graphitepowder as pore former showed uniform porosity to promote gas transmission, and the electrolyte waswell densified with a thickness of less than 10 m after sintered at 1250 C. The designed AT-SOECwas proved to work effectively for decomposing NO (3500 ppm, balanced in N2), and results indicatedthat the decomposition rate of NO increased with temperature and current, and the maximum NOdecomposition rate (99%) was obtained at 800 C.
机译:通过浸涂技术成功设计并制造了阳极支撑的管状固体氧化物电解槽(AT-SOEC),用于NO分解。 AT-SOEC包含多孔(La0.8Sr0.2)0.95MnO3(LSM95)作为阳极基板,LSM95 / 8 mol%氧化钇稳定的氧化锆(8YSZ)作为阳极活性层和阴极层,以及8YSZ作为电解质。 XRD图谱表明,LSM95和8YSZ在1250℃和NO气氛中具有良好的相稳定性,表明它们是用于NO分解的合适的电极和电解质材料。以石墨粉为成孔剂的电极显示出均匀的孔隙度以促进气体传输,并且在1250 C烧结后,电解质被致密化,厚度小于10 m。事实证明,设计的AT-SOEC可有效分解NO(3500 ppm,平衡)。在N2中),结果表明NO的分解速率随温度和电流的增加而增加,在800°C时获得最大的NO分解率(99%)。

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