过氧化物半衰期的测量和建模:一种热动力学方法

IF 1.5 4区 化学 Q4 CHEMISTRY, PHYSICAL
Florin Dan, Pranav Bagaria, Brian Habersberger, Amy Koziol
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引用次数: 0

摘要

有机过氧化物在高温条件下的半衰期值对表征反应性很重要,通常可以从文献或供应商处获得。然而,通常缺乏获得这些值的方法的细节/准确性,以及不同供应商和出版物的方法的差异,从而导致反应性概况的差异。为了解决这个问题,开发了一种包括量热实验和热力学建模的方法。目前的方法应用于五种过氧化物样品,以获得动力学参数并估计它们在感兴趣的温度范围内的半衰期。在非等温条件下,用DSC对稀过氧化物溶液(矿物油中~ 0.12 M)进行了测量,并根据三个基于模型和一个无模型的动力学方程对数据进行了动力学处理。各种动力学方法计算的半衰期吻合良好,但与文献中报道的动力学参数存在显著差异。此外,基于非等温测量建立的动力学模型得到的半衰期结果,通过等温量热测试进行了验证。鉴于我们的结果的准确性和稳健性,目前的方法可以应用于估计有机过氧化物在高温条件下的半衰期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Measurement and modeling of peroxides half-life: A thermo-kinetic approach

Half-life values of organic peroxides at elevated temperature conditions are important in characterizing the reactivity and are often available in literature or through vendors. However, there is often lack of details/accuracy on methods used to obtain these values, as well as differences in methods across vendors and publications, thus resulting in discrepant reactivity profile. To address this, a method involving calorimetric experiment and thermo-kinetic modeling was developed. The current approach was applied on five peroxides samples to obtain kinetic parameters and estimate their half-life in the temperature range of interest. The measurements were performed by DSC under non-isothermal conditions on the dilute peroxide solutions (∼0.12 M in mineral oil) and the data were kinetically treated according to three model-based and one model-free kinetic equations. A very good agreement was found between the half-life calculated by all kinetic methods, but significant differences were noticed with the kinetic parameters reported in literature. Additionally, the obtained half-life results, based on non-isothermal measurements developed kinetic models, were validated through isothermal calorimetric testing. Given the accuracy and robustness of our results, the current method can be applied to estimate half-life of organic peroxides at elevated temperature conditions.

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来源期刊
CiteScore
3.30
自引率
6.70%
发文量
74
审稿时长
3 months
期刊介绍: As the leading archival journal devoted exclusively to chemical kinetics, the International Journal of Chemical Kinetics publishes original research in gas phase, condensed phase, and polymer reaction kinetics, as well as biochemical and surface kinetics. The Journal seeks to be the primary archive for careful experimental measurements of reaction kinetics, in both simple and complex systems. The Journal also presents new developments in applied theoretical kinetics and publishes large kinetic models, and the algorithms and estimates used in these models. These include methods for handling the large reaction networks important in biochemistry, catalysis, and free radical chemistry. In addition, the Journal explores such topics as the quantitative relationships between molecular structure and chemical reactivity, organic/inorganic chemistry and reaction mechanisms, and the reactive chemistry at interfaces.
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