Abstract

AbstractSolid state kinetics lays its foundation on the basis of the experiments that are carried out in absolute isothermal conditions. However, although it is known that thermally activated processes involve gradual heating up of the reactants and the reactions progress under rising and fluctuating temperature conditions, conventional kinetic studies were confined to only isothermal conditions due to limitation of performing. In addition, the mathematical procedures developed for analysing non-isothermal kinetic data contain numerous approximations, assumptions and controversies [1–5]. These procedures fail to reflect the characteristics of a realistic situation. In addition to this, a priori knowledge of the reaction mechanism is required. The reaction mechanism is either assumed or identified by carrying out isothermal kinetic experiments. The methods [6–9] most widely used to evaluate activation energy from the non-isothermal calorimetric data are also based on a particular type of assumed mechanism. Nonetheless, characteristic reaction mechanism(s) do exist for all the reactions occurring under non-isothermal conditions. Therefore, the development of a more reliable and accurate non-isothermal kinetic analysis method is long overdue. In the present study, it has been shown that the actual reaction mechanism under non-isothermal conditions can be directly identified unambiguously through a newly developed technique.KeywordsConventional Kinetic StudiesIsothermal Kinetic ExperimentsSolid-state Reaction MechanismFluctuating Temperature ConditionsEvaluated Activation EnergyThese keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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