JOURNAL ARTICLE

Isothermal and nonisothermal melt‐crystallization kinetics of syndiotactic polystyrene

Qingyong ChenYingning YuTianhai NaHongfang ZhangZhishen Mo

Year: 2002 Journal:   Journal of Applied Polymer Science Vol: 83 (12)Pages: 2528-2538   Publisher: Wiley

Abstract

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 II→III transition, at a crystallization temperature of 239°, is found. The values of the nucleation parameter K g for regimes II and III are estimated. The lateral‐surface free energy, σ = 3.24 erg cm −2 , the fold‐surface free energy, σ e = 52.3 ± 4.2 erg cm −2 , and the average work of chain folding, q = 4.49 ± 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 Δ E = −830.7 kJ/mol and Δ E = −315.9 kJ/mol, respectively. © 2002 Wiley Periodicals, Inc. J Appl Polym Sci 83: 2528–2538, 2002

Keywords:
Polystyrene Crystallization Tacticity Nucleation Differential scanning calorimetry Materials science Activation energy Isothermal process Thermodynamics Kinetics Polymer chemistry Surface energy Kinetic energy Physical chemistry Chemistry Composite material Polymer Polymerization Physics

Metrics

27
Cited By
3.45
FWCI (Field Weighted Citation Impact)
30
Refs
0.90
Citation Normalized Percentile
Is in top 1%
Is in top 10%

Citation History

Topics

Polymer crystallization and properties
Physical Sciences →  Materials Science →  Polymers and Plastics
biodegradable polymer synthesis and properties
Physical Sciences →  Materials Science →  Biomaterials
Polymer Nanocomposites and Properties
Physical Sciences →  Materials Science →  Polymers and Plastics

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