包覆还原氧化石墨烯的高氯酸铵多步热分解的无模型动力学分析

IF 1.7 4区 化学 Q4 CHEMISTRY, PHYSICAL
Hamdane Akbi, Souleymen Rafai, Ahmed Mekki, Slimane Bekhouche, Sabri Touidjine, Elamine Louafi, Ahmed Saim, Mohamed Abderrahim Hamouche
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引用次数: 0

摘要

本研究探讨了在 AP 上涂覆 RGO 对其热分解动力学和行为的影响。在几种加热速率下,对纯 AP 和 AP@RGO 进行了差示扫描量热法(DSC)测定。采用数学解卷积法将 AP@RGO 在不同加热速率下的 DSC 曲线拆分为单个反应。采用有效的无模型方法 (MFA),对 AP 和 AP@RGO 的各种反应的动力学三元组进行了评估。AP@RGO 的 DSC 曲线解卷积显示了三个不同的分解过程,而纯 AP 只有两个分解过程。值得注意的是,低温分解反应似乎是由 RGO 催化的,导致活化能从 164 kJ/g 急剧下降到 116 kJ/g。相反,高温分解反应仍未被催化,活化能从 177 kJ/g 微升至 188 kJ/g。在 AP 的热分解过程中,RGO 的催化效力会因 RGO 内部的结构转变及其在高氯酸存在下的降解而波动。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Model-free kinetic analysis of multi-step thermal decomposition of ammonium perchlorate coated with reduced graphene oxide

Model-free kinetic analysis of multi-step thermal decomposition of ammonium perchlorate coated with reduced graphene oxide

This study investigates the effect of coating AP with RGO on its thermal decomposition kinetics and behavior. Differential scanning calorimetry (DSC) was performed for pure AP and AP@RGO at several heating rates. DSC curves of AP@RGO for various heating rates were split into individual reactions using a mathematical deconvolution approach. The assessment of kinetic triplets of various reactions was accomplished for both AP and AP@RGO using an effective model-free approach (MFA). Deconvolution of the DSC curve for AP@RGO reveals three distinct decomposition processes, compared to only two observed in pure AP. Notably, the low-temperature decomposition reaction appears to be catalyzed by RGO, leading to a dramatic decrease in activation energy from 164 to 116 kJ/g. Conversely, the high-temperature decomposition remains uncatalyzed, with a slight increase in activation energy from 177 to 188 kJ/g. The catalytic effectiveness of RGO in the thermal decomposition process of AP fluctuates due to structural transformations within RGO and its degradation in the presence of perchloric acid.

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来源期刊
CiteScore
3.30
自引率
5.60%
发文量
201
审稿时长
2.8 months
期刊介绍: Reaction Kinetics, Mechanisms and Catalysis is a medium for original contributions in the following fields: -kinetics of homogeneous reactions in gas, liquid and solid phase; -Homogeneous catalysis; -Heterogeneous catalysis; -Adsorption in heterogeneous catalysis; -Transport processes related to reaction kinetics and catalysis; -Preparation and study of catalysts; -Reactors and apparatus. Reaction Kinetics, Mechanisms and Catalysis was formerly published under the title Reaction Kinetics and Catalysis Letters.
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