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Catalytic decomposition of N2O over Ni and Mg-magnetite catalysts

机译:Ni和Mg磁铁矿催化剂上N2O的催化分解

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The total decomposition of N2Owas performed on the partially nanocrystalline substituted M_xFe_(3-x)O4 magnetite (M~(2+)= Ni~(2+) and Mg~(2+) with x = 0-1). The given results showed that the partial incorporation of Fe~(2+) by Ni~(2+) and Mg~(2+) into Fe3O4 spinel frameworks led to a significant amelioration in the catalytic activity for the N2O catalytic reaction. Furthermore, the catalytic activity of synthesized substrates depended on the Fe~(2+) substitution amount by Ni~(2+) and Mg~(2+) cations. The N2O conversion reached 20% (chemical regime) over the Ni0.75Fe2.25O4 and Mg0.58Fe2.42O4 catalysts at 395 and 404 K for N2O (5000 ppm), respectively. A relative increase of decomposition temperatures was observed after O2 addition. Moreover, other results show that the N2O conversion shifted to higher temperatures at high space velocities.
机译:在部分纳米晶体上执行的N2OWA的总分解,用X = 0-1取代了M_XFE_(3-X)O4磁铁矿(M〜(2+)= Ni〜(2+)和Mg〜(2+),用X = 0-1)。 给定的结果表明,Ni〜(2+)和Mg〜(2+)将Fe〜(2+)的部分结合到Fe3O4尖晶石框架中,导致N2O催化反应的催化活性显着改善。 此外,合成底物的催化活性取决于Ni〜(2+)和Mg〜(2+)阳离子的Fe〜(2+)替代量。 N2O转换分别在Ni0.75Fe2.25O4和MG0.58FE2.42O4催化剂395和404 K的N2O(5000 ppm)上达到20%(化学状态)。 添加O2后观察到分解温度的相对升高。 此外,其他结果表明,在高空间速度下,N2O转换转移到了较高的温度。

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