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首页> 外文期刊>Journal of Alloys and Compounds: An Interdisciplinary Journal of Materials Science and Solid-state Chemistry and Physics >The excellent catalytic activity for thermal decomposition of ammonium perchlorate using porous CuCo2O4 synthesized by template-free solution combustion method
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The excellent catalytic activity for thermal decomposition of ammonium perchlorate using porous CuCo2O4 synthesized by template-free solution combustion method

机译:使用模板 - 无孔溶液燃烧法合成的多孔Cuco2O4热分解铵热分解的优异催化活性

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摘要

Spinel CuCo2O4 with 3D macro-/mesoporous structure has been successfully synthesized via template-free solution combustion method. X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), and N-2 absorption/desorption have been done to obtain compositional and morphological information as well as BET surface area of the as-synthesized sample. Catalytic activities of the porous CuCo2O4 towards the thermal decomposition of ammonium perchlorate (AP) were investigated with differential scanning calorimetry (DSC) and thermogravimetry (TG) techniques. The results show that the addition of spinel CuCo2O4 with 3D macro-/nanoporousstructure to AP remarkably decreases the high temperature decomposition (HTD) from 470.92 degrees C for pure AP to 308.74 degrees C for AP containing CuCo2O4 additive with a mass ratio of 2%. The as-synthesized 3D macro-/nanoporous spinel CuCo2O4 is the promising type of catalytic materials for AP-based composite solid rocket propellants. The simple synthesis method is conducive to large-scale industrial production for application in AP thermal decomposition. (C) 2019 Elsevier B.V. All rights reserved.
机译:通过无模板溶液燃烧方法成功地合成了具有3D宏观/中孔结构的尖晶石Cuco2O4。已经进行了X射线衍射(XRD),扫描电子显微镜(SEM),透射电子显微镜(TEM)和N-2吸收/解吸,以获得组成和形态学信息以及合成样品的BET表面积。采用差示扫描量热法(DSC)和热重率(TG)技术研究了多孔CUCO2O4朝向高氯酸铵(AP)的热分解的催化活性。结果表明,对于370.92℃,将纯净的AP至308.74摄氏度的高温分解(HTD)与含有2%的含量比例为2%的AP的AP,将具有37.92℃的高温分解(HTD)的尖晶石Cuco2O4从470.92℃加入到308.74摄氏度。 AS合成的3D宏/纳米孔尖晶石Cuco2O4是用于基于AP的复合固体火箭推进剂的有希望的催化材料。简单的合成方法有利于大规模工业生产,在AP热分解中应用。 (c)2019 Elsevier B.v.保留所有权利。

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