2014
DOI: 10.1016/j.tca.2014.05.016
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Accelerated testing of thermo-oxidative degradation of polyvinyl butyral

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Cited by 20 publications
(6 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: 68%
“…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: 68%
“…The degradation temperature is identified at 641 K, whose decomposition products correspond mainly to butyraldehyde and acetic acid, due to the degradation of butyral and acetate units of polymer chains, respectively. At a temperature above 741 K, the sample degrades completely [ 34 , 35 ]. The presence of water was not detected, since no significant decrease in weight loss at the boiling temperature was observed.…”
Section: Resultsmentioning
confidence: 99%
“…For polymer materials suitable for the Arrhenius model, the typical value of activation energy during thermal aging is 0.75–1.6 eV, that is, 72–153 kJ mol −1 , and even Janting 28 et al have studied medical device polymer that the activation energy of thermal aging is 0.67 eV, 64.32 kJ mol −1 . Liau 21 and Ivanov 23 used the characterization method of thermogravimetry and obtained the activation energy of about 200 kJ mol −1 through rapid thermal decomposition at high temperatures. The value of activation energy obtained cannot reflect the aging process of PVB under constant temperature.…”
Section: Resultsmentioning
confidence: 99%
“…According to ref. 23 , 31 and 33 , PVB can be decomposed into n -butyraldehyde, butyric acid, acetic acid, n -butanol, and other substances under high-temperature thermal degradation.…”
Section: Resultsmentioning
confidence: 99%