Nawel Matmat, Amir Abdelaziz, Djalal Trache, Ahmed Fouzi Tarchoun, Hani Boukeciat, Aziz Rahal
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引用次数: 0
摘要
本研究成功地阐述了一种基于硝化纤维素和硝化淀粉(NCNPS)双生物聚合物以及高氯酸铵(AP)的创新型高能复合材料,并对其进行了表征。通过 CEA-NASA 软件对弹道性能进行理论估算,确定了 AP@NCNPS 复合材料的最佳配方。随后,通过傅立叶变换红外光谱、二冷沉积和热重分析对获得的复合材料进行了全面表征。红外光谱显示了酯硝酸盐的所有特征基团,表明 AP 的加入并没有改变双生物聚合物的化学结构。热分析表明,加入氧化剂后,AP@NCNPS 复合材料所有分解阶段的最高降解温度都有所下降,这证明 AP 与 NCNPS 生物聚合物基质之间存在相互催化作用。使用线性和非线性等转换方法(TAS、VYA/CE)进行的热动力学研究表明,活化能值大大降低,再次凸显了 AP 在改善 AP@NCNPS 高能复合材料热分解过程中的作用。
Elaboration, spectroscopic characterization, and study of the thermal decomposition process of energetic composites based on ammonium perchlorate and dual-biopolymers
The current study presents a successful elaboration and characterization of an innovative energetic composite based on nitrocellulose and nitrostarch (NCNPS) dual-biopolymers, and ammonium perchlorate (AP). A pre-establishment of the optimal formulation of the AP@NCNPS composite has been determined through a theoretical estimation of the ballistic performance via CEA-NASA software. The obtained composites were then fully characterized by FTIR, DSC, and TGA analyses. The IR-spectroscopy depicted the presence of all the characteristic groups of ester nitrates, revealing that the incorporation of AP did not alter the chemical structure of the dual-biopolymers. The thermal analysis demonstrated a mutual catalytic effect between AP and NCNPS biopolymeric matrix supported by the decrease of the maximum degradation temperatures observed for all the decomposition stages of AP@NCNPS composite after the incorporation of the oxidizer. The thermo-kinetic investigation, carried out using linear and non-linear isoconversional approaches (TAS, VYA/CE) demonstrated a considerable reduction in the activation energy values, highlighting, once again the role of AP in the improvement of the thermolysis process of the prepared AP@NCNPS energetic composite.