二茂铁基催化剂对高压燃烧高氯酸铵/羟基端聚丁二烯/铝复合推进剂传热的影响

IF 5 Q1 ENGINEERING, MULTIDISCIPLINARY
Jinchao Han, Songqi Hu, Linlin Liu
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引用次数: 0

摘要

调节高氯酸铵/羟基封端聚丁二烯/铝(AP/HTPB/Al)复合推进剂在高压下的燃烧速率压力指数是其应用于高压固体火箭发动机的关键步骤。在这项工作中,研究了含有二茂铁基催化剂的 AP/HTPB/Al 复合推进剂的燃烧特性,包括 7-28 MPa 范围内的燃烧速率、热行为、局部传热和温度曲线。结果表明,在添加正催化剂(Ce-Fc-MOF)、燃烧速率抑制剂((二茂铁甲基)三甲基溴化铵,FcBr)和 FcBr/catocene 混合物(GFP)后,推进剂中仍能观察到指数断裂。然而,当推进剂中添加 Ce-Fc-MOF、FcBr 和 FcBr/GFP 时,特征压力增加,指数从 1.14 降至 0.66、0.55 和 0.48。此外,与纯 AP 相比,AP/FcBr 混合物和 AP/FcBr/GFP 混合物在第一分解阶段的温度分别提高了 7.50 ℃ 和 11.40 ℃。另一方面,AP/FcBr 和 AP/FcBr/GFP 混合物在第二分解阶段的温度分别降低了 48.30 ℃ 和 81.70 ℃。研究还发现,FcBr 可能会产生氨气覆盖 AP 表面。在这种情况下,FcBr 中的甲基与高氯酸发生反应,导致 AP 表面出现更多的氨,从而抑制了氨的解吸。此外,在添加催化剂的低压和高压条件下,淬火表面的 AP 粗颗粒相对于粘合剂基体呈凹形。在此过程中,只有添加 Ce-Fc-MOF 的推进剂才会出现 AP/HTPB 界面的下降。含有催化剂的推进剂的气相温度梯度比在低于和高于特征压力时显著降低,而不是空白推进剂的 3.6 倍。总之,研究结果表明,在高压和低压条件下,通过调整推进剂的局部传热和传质,可以有效地调节和控制压力指数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The regulation of ferrocene-based catalysts on heat transfer in high-pressure combustion of ammonium perchlorate/hydroxyl-terminated polybutadiene/aluminum composite propellants

The regulation of the burning rate pressure exponent for the ammonium perchlorate/hydroxyl-terminated polybutadiene/aluminum (AP/HTPB/Al) composite propellants under high pressures is a crucial step for its application in high-pressure solid rocket motors. In this work, the combustion characteristics of AP/HTPB/Al composite propellants containing ferrocene-based catalysts were investigated, including the burning rate, thermal behavior, the local heat transfer, and temperature profile in the range of 7–28 MPa. The results showed that the exponent breaks were still observed in the propellants after the addition of positive catalysts (Ce-Fc-MOF), the burning rate inhibitor ((Ferrocenylmethyl)trimethylammonium bromide, FcBr) and the mixture of FcBr/catocene (GFP). However, the characteristic pressure has increased, and the exponent decreased from 1.14 to 0.66, 0.55, and 0.48 when the addition of Ce-Fc-MOF, FcBr and FcBr/GFP in the propellants. In addition, the temperature in the first decomposition stage was increased by 7.50 °C and 11.40 °C for the AP/FcBr mixture and the AP/FcBr/GFP mixture, respectively, compared to the pure AP. On the other hand, the temperature in the second decomposition stage decreased by 48.30 °C and 81.70 °C for AP/FcBr and AP/FcBr/GFP mixtures, respectively. It was also found that FcBr might generate ammonia to cover the AP surface. In this case, a reaction between the methyl in FcBr and perchloric acid caused more ammonia to appear at the AP surface, resulting in the suppression of ammonia desorption. In addition, the coarse AP particles on the quenched surface were of a concave shape relative to the binder matrix under low and high pressures when the catalysts were added. In the process, the decline at the AP/HTPB interface was only exhibited in the propellant with the addition of Ce-Fc-MOF. The ratio of the gas-phase temperature gradient of the propellants containing catalysts was reduced significantly below and above the characteristic pressure, rather than 3.6 times of the difference in the blank propellant. Overall, the obtained results demonstrated that the pressure exponent could be effectively regulated and controlled by adjusting the propellant local heat and mass transfer under high and low pressures.

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来源期刊
Defence Technology(防务技术)
Defence Technology(防务技术) Mechanical Engineering, Control and Systems Engineering, Industrial and Manufacturing Engineering
CiteScore
8.70
自引率
0.00%
发文量
728
审稿时长
25 days
期刊介绍: Defence Technology, a peer reviewed journal, is published monthly and aims to become the best international academic exchange platform for the research related to defence technology. It publishes original research papers having direct bearing on defence, with a balanced coverage on analytical, experimental, numerical simulation and applied investigations. It covers various disciplines of science, technology and engineering.
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