2017
DOI: 10.1134/s1560090417030083
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Colorimetric analysis of thermal degradation of plasticized poly(vinyl chloride): Potentials and limitations

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Cited by 6 publications
(5 citation statements)
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“…This actually means that the activation energy depends on the degree of coloring (conversion degree). A similar phenomenon of the activation energy dependence on the conversion degree, in particular, is well known for the thermal decomposition processes studied by thermogravimetric analysis [33,34,35]. Based on the natural assumption that for photodegradation of the composite as well as the photo and thermal degradation of polymeric materials considered as examples in [32], the Arrhenius law is satisfied, and the activation energy E α at the conversion degree (degree of coloring), α, can be estimated by Equation (3): E α = R[(T 1 T 2 )/(T 2 − T 1 )]lnk α , where T 2 and T 1 are the temperatures at which photodegradation occurs; k α = t 2 /t 1 is the acceleration factor; t 2 and t 1 are the times at which a certain degree of conversion, α (a certain value of the color difference ΔE), is reached at temperatures T 2 and T 1 ; and R is the gas constant.…”
Section: Resultsmentioning
confidence: 66%
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“…This actually means that the activation energy depends on the degree of coloring (conversion degree). A similar phenomenon of the activation energy dependence on the conversion degree, in particular, is well known for the thermal decomposition processes studied by thermogravimetric analysis [33,34,35]. Based on the natural assumption that for photodegradation of the composite as well as the photo and thermal degradation of polymeric materials considered as examples in [32], the Arrhenius law is satisfied, and the activation energy E α at the conversion degree (degree of coloring), α, can be estimated by Equation (3): E α = R[(T 1 T 2 )/(T 2 − T 1 )]lnk α , where T 2 and T 1 are the temperatures at which photodegradation occurs; k α = t 2 /t 1 is the acceleration factor; t 2 and t 1 are the times at which a certain degree of conversion, α (a certain value of the color difference ΔE), is reached at temperatures T 2 and T 1 ; and R is the gas constant.…”
Section: Resultsmentioning
confidence: 66%
“…A sharp increase or decrease of the test temperature didnot lead to unexpected effects: The coloring proceeded at a rate typical of this new temperature mode. In this respect, PPS is different from polyvinyl chloride, which is also strongly colored at elevated temperatures, but for which both the enhancement and weakening of color with the change of aging temperature were observed [34,35].…”
Section: Resultsmentioning
confidence: 99%
“…Более детальный анализ позволил установить, что окрашивание возникает и при более низкой температуре 100-110 °С [6,7]. Показано также, что регистрируемые изменения цветового различия ΔE определяются лавным образом увеличением ∆b*, характеризующим возрастание степени желтизны образцов.…”
Section: деструкция при высоких температурахunclassified
“…Развиваемые в последнее время подходы включают анализ кинетических закономерностей изменения ΔE и цветовых координат [6][7][8][9][10]. Определяемые кинетические параметры и зависимости кинетики от условий, в которых протекает деструкция, используются для выявления роли основных внешних факторов и компонентов материала в процессах изменения цветовых характеристик, что позволяет оценить их влияние на образование ПСС и других продуктов деструкции.…”
Section: Introductionunclassified
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