Determining Preexponential Factor in Model-Free Kinetic Methods: How and Why?

The kinetics of thermally stimulated processes in the condensed phase is commonly analyzed by model-free techniques such as isoconversional methods. Oftentimes, this type of analysis is unjustifiably limited to probing the activation energy alone, whereas the preexponential factor remains unexplored...

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Main Author: Sergey Vyazovkin
Format: Article
Language:English
Published: MDPI AG 2021-05-01
Series:Molecules
Subjects:
Online Access:https://www.mdpi.com/1420-3049/26/11/3077
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spelling doaj-cd3fb97c004b490b9f3c6733c148b39d2021-06-01T00:42:03ZengMDPI AGMolecules1420-30492021-05-01263077307710.3390/molecules26113077Determining Preexponential Factor in Model-Free Kinetic Methods: How and Why?Sergey Vyazovkin0Department of Chemistry, University of Alabama at Birmingham, 901 S. 14th Street, Birmingham, AL 35294, USAThe kinetics of thermally stimulated processes in the condensed phase is commonly analyzed by model-free techniques such as isoconversional methods. Oftentimes, this type of analysis is unjustifiably limited to probing the activation energy alone, whereas the preexponential factor remains unexplored. This article calls attention to the importance of determining the preexponential factor as an integral part of model-free kinetic analysis. The use of the compensation effect provides an efficient way of evaluating the preexponential factor for both single- and multi-step kinetics. Many effects observed experimentally as the reaction temperature shifts usually involve changes in both activation energy and preexponential factor and, thus, are better understood by combining both parameters into the rate constant. A technique for establishing the temperature dependence of the rate constant by utilizing the isoconversional values of the activation energy and preexponential factor is explained. It is stressed that that the experimental effects that involve changes in the preexponential factor can be traced to the activation entropy changes that may help in obtaining deeper insights into the process kinetics. The arguments are illustrated by experimental examples.https://www.mdpi.com/1420-3049/26/11/3077Arrhenius equationcrosslinking polymerization (curing)decompositiondegradationliquid and solid statephase transitions
collection DOAJ
language English
format Article
sources DOAJ
author Sergey Vyazovkin
spellingShingle Sergey Vyazovkin
Determining Preexponential Factor in Model-Free Kinetic Methods: How and Why?
Molecules
Arrhenius equation
crosslinking polymerization (curing)
decomposition
degradation
liquid and solid state
phase transitions
author_facet Sergey Vyazovkin
author_sort Sergey Vyazovkin
title Determining Preexponential Factor in Model-Free Kinetic Methods: How and Why?
title_short Determining Preexponential Factor in Model-Free Kinetic Methods: How and Why?
title_full Determining Preexponential Factor in Model-Free Kinetic Methods: How and Why?
title_fullStr Determining Preexponential Factor in Model-Free Kinetic Methods: How and Why?
title_full_unstemmed Determining Preexponential Factor in Model-Free Kinetic Methods: How and Why?
title_sort determining preexponential factor in model-free kinetic methods: how and why?
publisher MDPI AG
series Molecules
issn 1420-3049
publishDate 2021-05-01
description The kinetics of thermally stimulated processes in the condensed phase is commonly analyzed by model-free techniques such as isoconversional methods. Oftentimes, this type of analysis is unjustifiably limited to probing the activation energy alone, whereas the preexponential factor remains unexplored. This article calls attention to the importance of determining the preexponential factor as an integral part of model-free kinetic analysis. The use of the compensation effect provides an efficient way of evaluating the preexponential factor for both single- and multi-step kinetics. Many effects observed experimentally as the reaction temperature shifts usually involve changes in both activation energy and preexponential factor and, thus, are better understood by combining both parameters into the rate constant. A technique for establishing the temperature dependence of the rate constant by utilizing the isoconversional values of the activation energy and preexponential factor is explained. It is stressed that that the experimental effects that involve changes in the preexponential factor can be traced to the activation entropy changes that may help in obtaining deeper insights into the process kinetics. The arguments are illustrated by experimental examples.
topic Arrhenius equation
crosslinking polymerization (curing)
decomposition
degradation
liquid and solid state
phase transitions
url https://www.mdpi.com/1420-3049/26/11/3077
work_keys_str_mv AT sergeyvyazovkin determiningpreexponentialfactorinmodelfreekineticmethodshowandwhy
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