Stereocomplex Crystallization of Star‐Shaped 4‐Armed Equimolar Stereo Diblock Poly(lactide)s with Different Molecular Weights: Isothermal Crystallization from the Melt
Author(s) -
Tsuji Hideto,
Matsumura Nobutsugu
Publication year - 2016
Publication title -
macromolecular chemistry and physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.57
H-Index - 112
eISSN - 1521-3935
pISSN - 1022-1352
DOI - 10.1002/macp.201600042
Subject(s) - crystallization , crystallinity , crystallite , branching (polymer chemistry) , materials science , differential scanning calorimetry , polymer , polymer chemistry , isothermal process , crystallization of polymers , lactide , chemical engineering , optical microscope , crystallography , composite material , scanning electron microscope , polymerization , chemistry , thermodynamics , physics , engineering , metallurgy
The isothermal crystallization of star‐shaped four‐armed equimolar stereo diblock poly(lactide) (4‐LD) polymers with different molecular weights is investigated. Solely stereocomplex (SC) crystallites are formed in all equimolar 4‐LD polymers, irrespective of molecular weight and crystallization temperature ( T c ). The wide‐angle X‐ray diffractometry, differential scanning calorimetry, and polarized optical microscopy results for crystalline species, crystallinity, and maximum radial growth rate of spherulites values indicate that both branching and diblock architectures disturb the SC crystallization and spherulites growth of equimolar 4‐LD polymers, and the disturbance effect is larger for branching architecture than for diblock architecture. The equilibrium melting temperature ( T m 0 ) values are 181.9–266.0 °C, which are comparable with or lower than the value reported earlier (279 °C). The crystallite growth geometries of equimolar of 4‐LD polymers are independent of molecular weight and T c .