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首页> 外文期刊>Applied Catalysis, B. Environmental: An International Journal Devoted to Catalytic Science and Its Applications >Structural modification of LaCoO3 perovskite for oxidation reactions: The synergistic effect of Ca2+ and Mg2+ co-substitution on phase formation and catalytic performance
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Structural modification of LaCoO3 perovskite for oxidation reactions: The synergistic effect of Ca2+ and Mg2+ co-substitution on phase formation and catalytic performance

机译:LaCoO3钙钛矿用于氧化反应的结构修饰:Ca2 +和Mg2 +共取代对相形成和催化性能的协同作用

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Ca2+ and/or Mg2+ modified LaCoO3 perovskites were synthesized via a continuous supercritical water (sc-H2O) route, followed by a suite of heat-treatment processes. Experimental results revealed that the introductions of Ca2+ and Mg2+ had profoundly hindered the crystal growths of La(OH)(3) and Co(OH)(2) crystallites in sc-H2O environment where the extra Mg(OH)(2) had provided a confined platform for their reaction, effectively facilitating the formation of phase pure LaCoO3 perovskite. The synergistic effect as induced by dual-site substitution of Ca2+ and Mg2+ was proven very beneficial for suprafacial oxidation process, which had reduced the apparent activation energy (Ea) of LaCoO3 to only 34 kJ/mol in toluene oxidation. This is comparable to some noble metal catalysts. However, the dual-site substitution had somehow deactivated the intrafacial reaction process as the co-substituted Ca2+ had inhibited the generation of surface lattice oxygen and decreased the reducibility of LaCoO3 perovskite. (C) 2015 Elsevier B.V. All rights reserved.
机译:Ca2 +和/或Mg2 +改性的LaCoO3钙钛矿是通过连续的超临界水(sc-H2O)路线合成的,然后进行一系列热处理。实验结果表明,在sc-H2O环境中,Ca2 +和Mg2 +的引入严重阻碍了La(OH)(3)和Co(OH)(2)晶体的晶体生长,在该环境中提供了额外的Mg(OH)(2)。一个封闭的反应平台,有效促进相纯LaCoO3钙钛矿的形成。事实证明,Ca2 +和Mg2 +的双位取代引起的协同作用对于表面氧化过程非常有利,该过程将LaCoO3的表观活化能(Ea)在甲苯氧化中降低到仅34 kJ / mol。这可与某些贵金属催化剂相比。然而,由于共取代的Ca2 +抑制了表面晶格氧的生成并降低了LaCoO3钙钛矿的还原性,因此双位取代使界面反应过程失活了。 (C)2015 Elsevier B.V.保留所有权利。

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