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Study of the decomposition of phase stabilized ammonium nitrate (PSAN) by simultaneous thermal analysis: determination of kinetic parameters

机译:同时热分析法测定相稳态硝酸铵(psaN)的分解:动力学参数的测定

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摘要

Ammonium nitrate (AN) has been extensively used both in explosive and propellant formulations. Unlike AN, there is a lack of information about the thermal decomposition and related kinetic analysis of phase stabilized ammonium nitrate (PSAN). Simultaneous thermal analysis (DSC-TG) has been used in the thermal characterisation of a specific type of PSAN containing 1.0% of NiO (stabilizing agent) and 0.5% of Petro (anti-caking agent) as additives. Repeated runs covering the nominal heating rates range from 2.5 to 20 K min-1 allowed to conclude on the good reproducibility of the main features of the thermal behavior of PSAN, i.e., two phase transitions, melting and decomposition. Non-isothermal kinetic analysis has been used to estimated the Arrhenius parameters of the decomposition process by applying both a single curve method and two isoconversion methods to the TG data. The results are discussed considering the range of applicability of the methods as well as the influence of the experimental conditions and/or techniques in the kinetic analysis results in a broader sense. A systematic approach based on the isoconversion methods results and statistical tools has been adopted to obtain reliable estimates of the Arrhenius parameters for the thermal decomposition of PSAN. Under the condition of study, the values of 81.4±3.5 kJ mol-1 for the activation energy and (5.63±0.01)×105 s-1 for the pre-exponential factor were found as describing the process over a wide range of the kinetic analysis.
机译:硝酸铵(AN)已广泛用于炸药和推进剂配方中。与AN不同,缺少有关相稳定硝酸铵(PSAN)的热分解和相关动力学分析的信息。同时热分析(DSC-TG)已用于特定类型的PSAN的热表征,该PSAN包含1.0%的NiO(稳定剂)和0.5%的Petro(抗结块剂)作为添加剂。重复运行涵盖2.5至20 K min-1的额定加热速率,可以得出PSAN热行为主要特征的良好再现性,即两个相变,熔化和分解。通过将单曲线方法和两种等转换方法都应用于TG数据,非等温动力学分析已用于估算分解过程的Arrhenius参数。从更广泛的意义上考虑方法的适用范围以及实验条件和/或技术对动力学分析结果的影响来讨论结果。已采用基于等转换方法结果和统计工具的系统方法来获得对PSAN热分解的Arrhenius参数的可靠估计。在研究条件下,发现活化能为81.4±3.5 kJ mol-1,指数前因子为(5.63±0.01)×105 s-1,可以描述整个动力学范围内的过程分析。

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