Nonisothermal melt crystallization kinetics of PEDEKmK linked by metaphenyl and biphenyl was investigated by differential scanning calorimetry (DSC). A convenient and reasonable kinetic approach was used to describe the nonisothermal melt crystallization behavior, and its applicability was verified
Crystallization behavior of a novel poly(aryl ether ketone): PEDEKmK
โ Scribed by Tianxi Liu; Zhishen Mo; Shanger Wang; Hongfang Zhang; Junzuo Wang; Hui Na; Zhongwen Wu
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 247 KB
- Volume
- 64
- Category
- Article
- ISSN
- 0021-8995
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โฆ Synopsis
Isothermal melt and cold crystallization kinetics of PEDEKmK linked by meta-phenyl and biphenyl were investigated by differential scanning calorimetry in two temperature regions. Avrami analysis is used to describe the primary stages of the melt and cold crystallization, with exponent n ร 2 and n ร 4, respectively. The activation energies are 0118 kJ/mol and 510 kJ/mol for crystallization from the melt and the glassy states, respectively. The equilibrium melting point T 0 m is estimated to be 309ะC by using the Hoffman-Weeks approach, which compares favorably with determination from the Thomson-Gibbs method. The lateral and end surface free energies derived from the Lauritzen-Hoffman spherulitic growth rate equation are s ร 8.45 erg/cm 2 and s e ร 45.17 erg/cm 2 , respectively. The work of chain folding q is determined as 3.06 kcal/mol. These observed crystallization characteristics of PEDEKmK are compared with those of the other members of poly(aryl ether ketone) family.
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The isothermal melt and cold crystallization kinetics of poly(aryl ether ketone ether ketone ketone) are investigated by differential scanning calorimetry over two temperature regions. The Avrami equation describes the primary stage of isothermal crystallization kinetics with the exponent n ฯท 2 for