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由液化导致的表观自催化作用:3,4,5-三硝基吡唑酸铵的热分解

Apparent autocatalysis due to liquefaction: thermal decomposition of ammonium 3,4,5-trinitropyrazolate.

作者信息

Muravyev Nikita V, Monogarov Konstantin A, Dalinger Igor L, Koga Nobuyoshi, Pivkina Alla N

机构信息

N.N. Semenov Federal Research Center for Chemical Physic, Russian Academy of Sciences, 4 Kosygina Str., Moscow 119991, Russia.

N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 47 Leninsky Ave., Moscow 119991, Russia.

出版信息

Phys Chem Chem Phys. 2021 May 26;23(20):11797-11806. doi: 10.1039/d1cp01530c.

Abstract

Thermal decomposition of solids is often accompanied by autocatalysis, one of the possible causes of which is the formation of a liquid phase. The kinetic model considering the liquefaction of solid reactants under isothermal conditions was proposed by Bawn in the 1950s. The present study reports the application of the Bawn model to the thermolysis of 3,4,5-trinitropyrazole ammonium salt (ATNP) under nonisothermal conditions. The thermal decomposition of ATNP is comprised of low-temperature and high-temperature stages. The low-temperature stage exhibits two distinct exothermic peaks in differential scanning calorimetry (DSC), fitted by two consecutive autocatalytic reactions with a model-fitting kinetic analysis. The liquefaction of the solid reactant during the first reaction is directly observed, giving mechanistic evidence for the Bawn model. We have expressed the Bawn model by a combination of two extended Prout-Tompkins (ePT) equations with the activation energy for the leading liquid-state reaction of Ea = 140.6 ± 0.3 kJ mol-1. The release of ammonia is detected from the beginning, suggesting that the thermal dissociation of ATNP to 3,4,5-trinitropyrazole is an initiation reaction of the thermal decomposition. We proposed ATNP liquefication, leading to the apparent autocatalytic behavior of the first global decomposition reaction, is caused by the eutectic formation between ATNP and 3,4,5-trinitropyrazole, as it was confirmed by DSC analysis of the artificial mixture. The presented approach of the combination of ePT formalism with a Bawn model is generally applicable to a broader range of thermal processes accompanied by liquid phase formation and apparent acceleration.

摘要

固体的热分解通常伴随着自催化作用,其可能的原因之一是液相的形成。20世纪50年代,鲍恩提出了考虑等温条件下固体反应物液化的动力学模型。本研究报道了鲍恩模型在3,4,5-三硝基吡唑铵盐(ATNP)非等温热解中的应用。ATNP的热分解包括低温和高温阶段。在差示扫描量热法(DSC)中,低温阶段呈现出两个明显的放热峰,通过模型拟合动力学分析用两个连续的自催化反应进行拟合。直接观察到了第一次反应过程中固体反应物的液化,为鲍恩模型提供了机理证据。我们用两个扩展的普劳特-汤普金斯(ePT)方程的组合来表示鲍恩模型,主导液相反应的活化能为Ea = 140.6 ± 0.3 kJ mol-1。从一开始就检测到了氨的释放,这表明ATNP热分解为3,4,5-三硝基吡唑是热分解的引发反应。我们提出,ATNP液化导致了第一次整体分解反应的表观自催化行为,这是由ATNP与3,4,5-三硝基吡唑之间形成共晶引起的,这已通过人工混合物的DSC分析得到证实。所提出的ePT形式与鲍恩模型相结合的方法通常适用于更广泛的伴有液相形成和表观加速的热过程。

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