Enhanced anti-migration performance of carbon nanotubes confined ferrocenyl compounds and their synergistic catalytic activity on the thermal decomposition of ammonium perchlorate

高氯酸铵 二茂铁 热分解 纳米复合材料 催化作用 材料科学 分解 碳纳米管 傅里叶变换红外光谱 无机化学 化学工程 热解 化学 核化学 有机化学 纳米技术 电化学 物理化学 电极 工程类
作者
Liying Yang,Ruizhe Xu,Zhiyuan Mi,Yuting Wan,Xiaolong Fu,Liping Jiang,Yajun Jian,Jizhen Li,Guofang Zhang
出处
期刊:Materials Today Chemistry [Elsevier]
卷期号:26: 101168-101168 被引量:4
标识
DOI:10.1016/j.mtchem.2022.101168
摘要

To retard high-migration issues of the commercialized ferrocene-based burning rate catalysts (BRCs), six commercial ferrocenyl derivatives (FcR), including catocene, N, N-dimethylaminomethyl ferrocene, n-butylferrocene, tert-butylferrocene, n-octylferrocene and ferrocene, were filled into carbon nanotubes (CNTs) by ultrasonication. The CNTs incorporated ferrocene nanocomposites ([email protected]) were characterized by TEM, SEM, BET, XPS, FTIR, Raman and XRD techniques, which indicated that the ferrocenes are successfully filled into the CNTs. The anti-migration and anti-volatility tests unveiled that the [email protected] exhibit neglectable migration tendency after four weeks of aging at 50 °C and low volatility when tested at 70 °C for 24 h. The combustion catalytic results displayed that the [email protected] nanocomposites play a vital role in promoting the thermal decomposition of ammonium perchlorate (AP), with the best one lowering the peak temperature of high-temperature decomposition stage (HTD) of AP by 114.2 °C and increasing its released heat by 160%. And it was found that the smaller the diameter of a CNT is, the lower the peak temperature of AP and the higher the released heat of AP. In addition, the decomposition mechanism of AP catalyzed by [email protected](L1) was studied by thermal decomposition kinetics, in-situ solid FTIR and TG-FTIR-MS methods. The results revealed that the nanocomposites can absorb more generated NH3 and HClO4 gases during AP decomposition with formation of superoxide anions (O2−), accelerating the oxidation of N2O to NO, and promoting the AP decomposition at lower temperature. Thus, a possible decomposition mechanism of AP catalyzed by [email protected] is proposed.
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