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Rational approximations of the integral of the Arrhenius function

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TLDR
Rational approximations have been derived for the integral of the Arrhenius function dT which is important in the kinetic analysis of thermogravimetric data and is found to be equivalent to the Gorbachev approximation.
Abstract
Rational approximations have been derived for the integral of the Arrhenius function $$\int\limits_0^T {\exp ( - E/RT)}$$ dT which is important in the kinetic analysis of thermogravimetric data. The first degree rational approximation is found to be equivalent to the Gorbachev approximation, i.e., RT2 exp (−E/RT)/(E+2RT). The second degree rational approximation is more accurate than the Zsako empirical approximation when E/RT 5. The third and higher degree rational approximations are found to be more accurate than any other previous approximation.

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Citations
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The applicability of Johnson-Mehl-Avrami model in the thermal analysis of the crystallization kinetics of glasses☆

Jiří Málek
- 01 Dec 1995 - 
TL;DR: In this paper, the applicability of the Johnson-Mehl-Avrami equation for non-isothermal crystallization kinetics has been investigated, and it has been shown that it has limited applicability for the nonisothermal transformations involving nucleation and growth.
Journal ArticleDOI

The ‘Temperature Integral’ — Its use and abuse

Joseph H. Flynn
- 15 Oct 1997 - 
TL;DR: A review of the history of the temperature dependence of reaction rate in reaction kinetics can be found in this article, where various equations which are in use today for expressing this dependence were delineated by van't Hoff almost one hundred years ago.
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Applicability of the master plots in kinetic analysis of non-isothermal data

TL;DR: In this article, the ability to determine the actual reaction mechanism (RM) of solid state processes from a single nonisothermal curve was analyzed and discussed, and it was found that the reaction follows the R3 mechanism which is in very good agreement with the results of isothermal experiments.
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Basics and Applications of Solid-State Kinetics: A Pharmaceutical Perspective

TL;DR: Controversies have arisen with regard to interpreting solid-state kinetic results, which include variable activation energy, calculation methods, and kinetic compensation effects.
Journal ArticleDOI

Cure kinetics of epoxy resins studied by non-isothermal DSC data

TL;DR: In this article, the curing kinetics of diglycidyl ether of bisphenol A (DGEBA) and DGEHQ epoxy resins in the presence of TETA as a reactive diluent and triethylenetetetramine (TETA) as the curing agent were studied by non-isothermal differential scanning calorimetry (DSC) technique at different heating rates.
References
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Journal ArticleDOI

Kinetic Parameters from Thermogravimetric Data

A. W. Coats, +1 more
- 01 Jan 1964 - 
TL;DR: In this article, a thermocouple is used to measure the sample temperature in a Stanton HT-D thermobalance, the bead of which is positioned in or near the sample, depending on crucible design.
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Empirical formula for the exponential integral in non-isothermal kinetics

TL;DR: The exponential integral of the exponential integral can be approximated by means of the empirical formula, e.g. as mentioned in this paper, which approximates p(x) = - \int\limits_\infty ^x {\frac{{e^{ - u} }}{{u^2 }}} \cdot du\).
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Reaction kinetics and differential thermal analysis

TL;DR: In this paper, the relationship between chemical kinetics and differential thermal analysis (DTA) curves is studied for the reactions which follow the general rate expression: r = r/sub 0/e/sup -E/RT/(1 - x).
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