高氯酸铵
材料科学
纳米复合材料
热分解
碳纳米管
傅里叶变换红外光谱
催化作用
化学工程
X射线光电子能谱
高分辨率透射电子显微镜
分解
热解
复合材料
纳米技术
复合数
有机化学
化学
透射电子显微镜
工程类
作者
Lufei Yang,Zhiyuan Mi,Haichao Fang,Ruizhe Xu,Binyang Lv,Jizhen Li,Guofang Zhang
标识
DOI:10.1016/j.surfin.2023.103642
摘要
For alleviating agglomeration of α-Fe2O3 nanoparticles and improving their catalytic activities as burning rate catalysts (BRCs) in solid propellants, Fe(CO)5 as the iron source was encapsulated into the inner space and/or loaded onto the outer surface of carbon nanotubes (CNTs) via ultrasonication with visible light and temperature control strategy. The Fe(CO)5-CNTs composites were subsequently transformed into α-Fe2O3-CNTs nanocomposites by Fe(CO)5 pyrolysis. The as-synthesized α-Fe2O3-CNTs composites were utterly characterized by HRTEM, SEM, BET, XPS, FTIR, Raman, and XRD. The catalytic combustion results show that the nanocomposites are highly active in boosting the thermal degradation of ammonium perchlorate (AP). α-Fe2O3&CNTs(S1) nanocomposite, the most excellent one, shifts left the peak temperature of the high-temperature decomposition (HTD) region of AP by 103.7 °C and increases its release heat by 190 %. Moreover, a carbon nanotube with a smaller outer diameter and higher iron content is conducive to enhancing AP thermal deterioration. A possible mechanism of AP decomposition with the addition of the nanocomposites was investigated by thermal decomposition dynamics, in-situ solid-state FTIR, and gas phase FTIR-MS technique. The mechanistic research implies that the produced NH3 and HClO4 gases can be absorbed on the nanocomposite surfaces to form more superoxide anions (O2−) during AP decomposition, accelerating the generation of NO from N2O and facilitating AP disintegration at a lower temperature. A tentative AP decomposition mechanism in the presence of the α-Fe2O3-CNTs nanocomposites is therefore proposed.
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