The lamellar morphological information and subsequent melting behaviour of syndiotactic polypropylene (s-PP) samples isothermally crystallized at crystallization temperatures ranging from 30 to 95 Β°C have been investigated using a combination of wide-angle X-ray diffraction (WAXD), smallangle X-ray
Isothermal and nonisothermal melt-crystallization kinetics of syndiotactic polystyrene
β Scribed by Qingyong Chen; Yingning Yu; Tianhai Na; Hongfang Zhang; Zhishen Mo
- Publisher
- John Wiley and Sons
- Year
- 2002
- Tongue
- English
- Weight
- 214 KB
- Volume
- 83
- Category
- Article
- ISSN
- 0021-8995
No coin nor oath required. For personal study only.
β¦ Synopsis
Abstract
Analyses of the isothermal and nonisothermal melt kinetics for syndiotactic polystyrene have been performed with differential scanning calorimetry, and several kinetic analyses have been used to describe the crystallization process. The regime IIβIII transition, at a crystallization temperature of 239Β°, is found. The values of the nucleation parameter K~g~ for regimes II and III are estimated. The lateralβsurface free energy, Ο = 3.24 erg cm^β2^, the foldβsurface free energy, Ο~e~ = 52.3 Β± 4.2 erg cm^β2^, and the average work of chain folding, q = 4.49 Β± 0.38 kcal/mol, are determined with the (040) plane assumed to be the growth plane. The observed crystallization characteristics of syndiotactic polystyrene are compared with those of isotactic polystyrene. The activation energies of isothermal and nonisothermal melt crystallization are determined to be Ξ__E__ = β830.7 kJ/mol and Ξ__E__ = β315.9 kJ/mol, respectively. Β© 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2528β2538, 2002
π SIMILAR VOLUMES
## Abstract The kinetics of the isothermal and nonisothermal cold crystallization of syndiotactic polystyrene (sβPS) were characterized with differential scanning calorimetry. A JohnsonβMehlβAvrami analysis of the isothermal experiments indicated that the cold crystallization of sβPS at a constant
## Abstract Nylon 10 12, a newly industrialized engineering plastic, shows a doubleβmelting phenomenon during melting. Partial melts were obtained when the sample was heated to the temperature between the two melting peaks. A differential scanning calorimeter was used to monitor the energies of the
Analysis of the isothermal, and nonisothermal crystallization kinetics of Nylon-11 is carried out using differential scanning calorimetry. The Avrami equation and that modified by Jeziorny can describe the primary stage of isothermal and nonisothermal crystallization of Nylon-11. In the isothermal c