Impacts of metal oxide crystalline structure on the decomposition of solid propellants under combustion heating rates

Fuel Communications Pub Date : 2024-06-01 Epub Date: 2024-03-27 DOI:10.1016/j.jfueco.2024.100112
Andrew R. Demko , Justin A. Lajoie , Alexander R. Jimenez-Thomas , David J. Ramirez , Travis R. Sippel
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Abstract

Ammonium perchlorate (AP) has been the oxidizer of choice for composite solid propellants for decades and has been the object of decomposition studies for safety monitoring. Typically, studies perform differential scanning calorimetry (DSC) or thermogravimetric analysis (TGA) to show how metal oxides (MO) commonly incorporated into propellants alter AP decomposition rates and completeness of reaction. Most past decomposition work studies temperatures below the crystal phase transition (240°C) from orthorhombic phase to cubic, which impose internal stresses within the lattice of AP particles. Phase change induces a partial decomposition, which does not follow a shrinking core behavior; instead, it develops a network of pores up to a few microns in size throughout. During low-temperature decomposition, particles lose approximately 30-40 % of their mass. Simultaneous DSC/TGA (STA) use low heating rates for combustion environments but offer information on MO's catalytic and electron transport modifications. This work demonstrates how the crystalline morphology MO additives mechanistically alter the combustion properties of composite propellants by identifying modes for promoting decomposition in AP and HTPB. MO morphology determines the electron structure of the molecule, which sets the band gap properties of the particles. This study evaluated different morphologies and a range of MOs to identify the most active MO for decomposing A.P. Kissinger analysis was applied using STA data at heating rates of 10-, 20-, and 30-°C/min revealing significant shift in the high-temperature decomposition with a range of metal oxides. Higher heating rates were evaluated using CO2 laser ignition to identify the time to first gas using the MO that offers the best heat absorption, such as the aluminum oxides. This higher heating rate was found do more accurately represent the changes in the combustion rates in the final propellant mixture. Additionally, it was shown that electron transport additives like CuO show the most significant impact on combustion, and thermal absorbers offer the lowest impact on AP/HTPB combustion. This understanding offers a new approach to propellant design not previously presented and suggests future testing for tailoring the use of metal oxides in propellants.

金属氧化物晶体结构对燃烧加热速率下固体推进剂分解的影响
几十年来,高氯酸铵(AP)一直是复合固体推进剂的首选氧化剂,也一直是安全监测分解研究的对象。通常,研究采用差示扫描量热法 (DSC) 或热重分析法 (TGA) 来显示推进剂中常见的金属氧化物 (MO) 如何改变 AP 的分解速率和反应完整性。过去的大多数分解工作研究的温度都低于从正方晶相到立方晶相的晶体相变温度(240°C),这在 AP 颗粒晶格内造成了内应力。相变会引起部分分解,这种分解并不遵循核心收缩的行为,而是在整个分解过程中形成一个孔隙网络,孔隙大小可达几微米。在低温分解过程中,颗粒会损失大约 30-40% 的质量。同时 DSC/TGA (STA) 对燃烧环境的加热速率较低,但可提供有关 MO 催化和电子传输修饰的信息。这项研究通过确定促进 AP 和 HTPB 分解的模式,展示了晶体形态 MO 添加剂如何从机理上改变复合推进剂的燃烧特性。MO 形态决定了分子的电子结构,而电子结构又决定了颗粒的带隙特性。本研究对不同的形态和一系列 MO 进行了评估,以确定分解 A.P.最活跃的 MO。利用加热速率为 10、20 和 30°C/min 时的 STA 数据进行了基辛格分析,结果显示一系列金属氧化物的高温分解发生了显著变化。使用 CO2 激光点火对更高的加热速率进行了评估,以确定使用铝氧化物等吸热效果最好的金属氧化物的初气时间。结果发现,这种较高的加热速率能更准确地反映最终推进剂混合物中燃烧速率的变化。此外,研究还表明,氧化铜等电子传输添加剂对燃烧的影响最大,而热吸收剂对 AP/HTPB 燃烧的影响最小。这一认识为推进剂设计提供了一种以前未曾提出过的新方法,并建议今后对推进剂中金属氧化物的使用进行定制测试。
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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