Monopropellant decomposition catalysts.: V.: Thermal decomposition and reduction of permanganates as models for the preparation of supported MnOx catalysts

被引:40
作者
Kappenstein, C
Pirault-Roy, L
Guérin, M
Wahdan, T
Ali, AA
Al-Sagheer, FA
Zaki, MI
机构
[1] CNRS, Catalyse Chim Organ Lab, Fac Sci, UMR Catalyse Met 6503, F-86022 Poitiers, France
[2] Inst Nat Resources & Environm Res, Riyadh, Saudi Arabia
[3] Kuwait Univ, Dept Chem, Fac Sci, Safat, Kuwait
关键词
hydrogen peroxide decomposition; manganese oxide catalysts; potassium permanganate; sodium permanganate; permanganate reduction; thermal decomposition;
D O I
10.1016/S0926-860X(02)00220-X
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The need for highly concentrated hydrogen peroxide solutions to fuel spacecraft propulsion systems necessitates the development of new catalytic formulations mainly based on supported manganese oxides. In order to improve the preparation of such catalysts, the thermal decomposition and the hydrothermal reduction of different permanganate precursors were studied, as well as the effect of washing on the products. The test samples were characterized by X-ray power diffraction (XRD) and surface area determination, and compared for their catalytic activity towards H2O2 decomposition using a constant pressure reactor (for 1.71% H2O2) and a constant volume reactor (for 50% H2O2). The catalysts prepared by thermal decomposition of KMnO4 or (NaMnO4H2O)-H-. have shown the intermediate formation of potassium (or sodium) manganate, and its partial dissolution during washing with water; higher catalytic activity and larger surface area were observed for the decomposition products of KMnO4. The hydrothermal reduction yielded products exhibiting larger surface area and higher specific catalytic activity when carried out under stoichiometric conditions. Comparable kinetic parameters were determined using both Catalytic reactors. Unsupported and alumina supported catalysts displayed comparable activity per gram of manganese. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:145 / 153
页数:9
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