Efficient thermal decomposition of ammonium perchlorate based on hollow spherical MnCo2O4.5 under carbon defect and morphology modulation

IF 6.7 1区 工程技术 Q2 ENERGY & FUELS
Fuel Pub Date : 2024-11-11 DOI:10.1016/j.fuel.2024.133666
Xin Yu , Zhengyi Zhao , Guofei Zhang , Sirong Li , Yanzhi Yang , Zhiyong Yan , Xin Tian , Xuechun Xiao
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引用次数: 0

Abstract

In this study, a one-step preparation of carbon-rich MnCo2O4.5 precursors are achieved by adding glucose in a hydrothermal environment. Subsequently, MnCo2O4.5 catalytic materials with different carbon defect contents are obtained by controlling the calcination temperature, which enables the simultaneous release of great heat during the thermal decomposition of catalytic AP. This specially designed MnCo2O4.5 catalytic material has a hollow structure and exhibits good dispersion and a large specific surface area. The high-temperature decomposition temperature (THTD) of ammonium perchlorate (AP) is reduced from 473.48 ℃ to 301.32 ℃ after adding 2 wt% catalytic materials. The catalytic materials resulte in a threefold increase in the decomposition heat release of AP (from 888.26 J·g−1 to 2616.98 J·g−1). It also reduced the activation energy (Ea) by half, from 296.8 kJ·mol−1 to 146.2 kJ·mol−1, greatly facilitating the reaction. Consequently, the reaction rate (k) is doubled, from 0.44 s−1 to 0.97 s−1. The bimetallic synergistic effect of MnCo2O4.5 itself, combined with the carbon material, significantly improved its performance in catalysing the thermal decomposition of AP. In addition, the combustion of carbon materials not only provides additional heat for AP pyrolysis but also further enhances the combustion of the Hydroxy Terminated Polybutadiene Composite Solid Propellant (HTPB-CSP) system. The introduction of this catalytic material reduces the CSP ignition delay time by 13 ms, allowing for a faster and more intense combustion process.
基于中空球形 MnCo2O4.5 的高氯酸铵在碳缺陷和形貌调制条件下的高效热分解
本研究通过在水热环境中加入葡萄糖,一步制备出富碳 MnCo2O4.5 前驱体。随后,通过控制煅烧温度,得到了不同碳缺陷含量的 MnCo2O4.5 催化材料,从而在催化 AP 的热分解过程中同时释放出大量热量。这种特殊设计的 MnCo2O4.5 催化材料具有中空结构,分散性好,比表面积大。添加 2 wt%的催化材料后,高氯酸铵(AP)的高温分解温度(THTD)从 473.48 ℃ 降至 301.32 ℃。催化材料使 AP 的分解放热量增加了三倍(从 888.26 J-g-1 增加到 2616.98 J-g-1)。它还将活化能(Ea)降低了一半,从 296.8 kJ-mol-1 降至 146.2 kJ-mol-1,大大促进了反应的进行。因此,反应速率(k)增加了一倍,从 0.44 s-1 增加到 0.97 s-1。MnCo2O4.5 本身与碳材料的双金属协同效应大大提高了其催化 AP 热分解的性能。此外,碳材料的燃烧不仅为 AP 热解提供了额外的热量,还进一步增强了羟基封端聚丁二烯复合固体推进剂(HTPB-CSP)系统的燃烧。引入这种催化材料后,CSP 的点火延迟时间缩短了 13 毫秒,使燃烧过程更快、更剧烈。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Fuel
Fuel 工程技术-工程:化工
CiteScore
12.80
自引率
20.30%
发文量
3506
审稿时长
64 days
期刊介绍: The exploration of energy sources remains a critical matter of study. For the past nine decades, fuel has consistently held the forefront in primary research efforts within the field of energy science. This area of investigation encompasses a wide range of subjects, with a particular emphasis on emerging concerns like environmental factors and pollution.
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