2002
DOI: 10.1016/s0165-2370(01)00183-8
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Kinetics of pyrolysis of high density polyethylene. Comparison of isothermal and dynamic experiments

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Cited by 135 publications
(75 citation statements)
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“…This can be explained with a kinetic compensation effect that can be expressed as a linear relationship between the logarithm of the pre-exponential factor and the activation energy (ln(A) = kE + b). This effect is mainly due to mathematical, physio-chemical, and experimental causes, which is widely researched [32,33]. Although this coupling of the kinetic parameters can result in similar values of the kinetic constant, the lower activation energy indicates the energy required to activate molecules to start the chemical reaction is lower because chemical reaction occurs on the condition that the molecular energy is equal to or higher than the activation energy.…”
Section: Conventional Pyrolysis Of Wpcbs Using Tgamentioning
confidence: 99%
“…This can be explained with a kinetic compensation effect that can be expressed as a linear relationship between the logarithm of the pre-exponential factor and the activation energy (ln(A) = kE + b). This effect is mainly due to mathematical, physio-chemical, and experimental causes, which is widely researched [32,33]. Although this coupling of the kinetic parameters can result in similar values of the kinetic constant, the lower activation energy indicates the energy required to activate molecules to start the chemical reaction is lower because chemical reaction occurs on the condition that the molecular energy is equal to or higher than the activation energy.…”
Section: Conventional Pyrolysis Of Wpcbs Using Tgamentioning
confidence: 99%
“…This linear heating rate program is the most widely used [28]. In any case, it is not uncommon to find in the literature a serious disagreement between the kinetic parameters calculated from data obtained under isothermal and non-isothermal conditions [26,29,30]. Sample Controlled Thermal Analysis (SCTA) constitutes an interesting non isothermal method which has been rarely applied to the kinetic analysis of thermal degradation of polymers [31].…”
Section: Introductionmentioning
confidence: 99%
“…Because of this complexity, a large number of papers found in the literature assume first order or norder kinetic models to describe the thermal degradation of polymers [8,23,30,34,[37][38][39][40][41][42][43][44][45], what would entail a non realistic description of the real reaction leading to erroneous kinetic parameters. Combined kinetic analysis is a procedure recently proposed that allows for the simultaneous analysis of a set of experimental curves recorded under any thermal schedule [27,[46][47][48].…”
Section: Introductionmentioning
confidence: 99%
“…The first step for a suitable design of any pyrolysis reactor is the knowledge of the process kinetics of the input plastic matrices. Many extensive studies on thermal degradation kinetics of single plastics have been carried out [12][13][14][15][16][17][18], and most of them have been developed on the assumption that the reaction can be described by a first or an nth order reaction model. This assumption can result in the Arrhenius parameters deviating from the real ones [19][20][21].…”
mentioning
confidence: 99%