Suppr超能文献

过碳酸钠热分解的放热行为:连续吸热和放热过程的动力学反褶积

Exothermic Behavior of Thermal Decomposition of Sodium Percarbonate: Kinetic Deconvolution of Successive Endothermic and Exothermic Processes.

作者信息

Nakano Masayoshi, Wada Takeshi, Koga Nobuyoshi

机构信息

Chemistry Laboratory, Department of Science Education, Graduate School of Education, Hiroshima University , 1-1-1 Kagamiyama, Higashi-Hiroshima 739-8524, Japan.

出版信息

J Phys Chem A. 2015 Sep 24;119(38):9761-9. doi: 10.1021/acs.jpca.5b07044.

Abstract

This study focused on the kinetic modeling of the thermal decomposition of sodium percarbonate (SPC, sodium carbonate-hydrogen peroxide (2/3)). The reaction is characterized by apparently different kinetic profiles of mass-loss and exothermic behavior as recorded by thermogravimetry and differential scanning calorimetry, respectively. This phenomenon results from a combination of different kinetic features of the reaction involving two overlapping mass-loss steps controlled by the physico-geometry of the reaction and successive endothermic and exothermic processes caused by the detachment and decomposition of H2O2(g). For kinetic modeling, the overall reaction was initially separated into endothermic and exothermic processes using kinetic deconvolution analysis. Then, both of the endothermic and exothermic processes were further separated into two reaction steps accounting for the physico-geometrically controlled reaction that occurs in two steps. Kinetic modeling through kinetic deconvolution analysis clearly illustrates the appearance of the net exothermic effect is the result of a slight delay of the exothermic process to the endothermic process in each physico-geometrically controlled reaction step. This demonstrates that kinetic modeling attempted in this study is useful for interpreting the exothermic behavior of solid-state reactions such as the oxidative decomposition of solids and thermal decomposition of oxidizing agent.

摘要

本研究聚焦于过碳酸钠(SPC,碳酸钠 - 过氧化氢(2/3))热分解的动力学建模。该反应的特征在于,热重分析法和差示扫描量热法分别记录的质量损失和放热行为具有明显不同的动力学曲线。这种现象是由该反应不同的动力学特征组合导致的,这些特征包括由反应的物理几何结构控制的两个重叠质量损失步骤,以及由H2O2(g)的脱离和分解引起的连续吸热和放热过程。对于动力学建模,首先使用动力学反褶积分析将整个反应分离为吸热和放热过程。然后,吸热和放热过程都进一步分离为两个反应步骤,以说明分两步发生的物理几何结构控制的反应。通过动力学反褶积分析进行的动力学建模清楚地表明,净放热效应的出现是每个物理几何结构控制的反应步骤中放热过程相对于吸热过程略有延迟的结果。这表明本研究中尝试的动力学建模对于解释固态反应的放热行为(如固体的氧化分解和氧化剂的热分解)是有用的。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验