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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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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