CRYSTAL STRUCTURE AND MORPHOLOGY OF NASCENT SAMPLES OF SYMMETRIC AROMATIC POLYESTERS——Ⅱ. POLY(p-PHENYLENE 2,6-NAPHTHALATE)*
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CRYSTAL STRUCTURE AND MORPHOLOGY OF NASCENT SAMPLES OF SYMMETRIC AROMATIC POLYESTERS——Ⅱ. POLY(p-PHENYLENE 2,6-NAPHTHALATE)*
CRYSTAL STRUCTURE AND MORPHOLOGY OF NASCENT SAMPLES OF SYMMETRIC AROMATIC POLYESTERS——Ⅱ. POLY(p-PHENYLENE 2,6-NAPHTHALATE)*
高分子科学(英文版)2003年21卷第2期 页码:205-221
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纸质出版:2003-04-20
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CRYSTAL STRUCTURE AND MORPHOLOGY OF NASCENT SAMPLES OF SYMMETRIC AROMATIC POLYESTERS——Ⅱ. POLY(p-PHENYLENE 2,6-NAPHTHALATE)*[J]. 高分子科学(英文版), 2003,21(2):205-221.
CRYSTAL STRUCTURE AND MORPHOLOGY OF NASCENT SAMPLES OF SYMMETRIC AROMATIC POLYESTERS——Ⅱ. POLY(p-PHENYLENE 2,6-NAPHTHALATE)*[J]. 2003, 21(2): 205-221.
CRYSTAL STRUCTURE AND MORPHOLOGY OF NASCENT SAMPLES OF SYMMETRIC AROMATIC POLYESTERS——Ⅱ. POLY(p-PHENYLENE 2,6-NAPHTHALATE)*[J]. 高分子科学(英文版), 2003,21(2):205-221.DOI:
CRYSTAL STRUCTURE AND MORPHOLOGY OF NASCENT SAMPLES OF SYMMETRIC AROMATIC POLYESTERS——Ⅱ. POLY(p-PHENYLENE 2,6-NAPHTHALATE)*[J]. 2003, 21(2): 205-221.DOI:
CRYSTAL STRUCTURE AND MORPHOLOGY OF NASCENT SAMPLES OF SYMMETRIC AROMATIC POLYESTERS——Ⅱ. POLY(p-PHENYLENE 2,6-NAPHTHALATE)*
Confined thin film melt polymerization (CTFMP) of naphthalene chloride/hydroquinone (NCMQ
1/1
molar)mixtures at polymerization temperatures (Tp) below ca. 300℃ resulted in relatively thick
elongated crystals. Polymerizationof NC/HQ above 300℃ between glass yielded well-formed lamellar crystals ca. 100 A thick. Phase Ⅰ and Ⅱ [001] EDpatterns were obtained for all Tp
the relative amount of phase Ⅰ increasing with Tp. Polymerization of naphthalenedicarboxylic acid/hydroquinione diacetate 1/1 mixtures at high Tp also yielded lamellar crystals that "curled up" off of the substrate.When the high temperature CTFMP polymerization was conducted between mica
aggregates of lamellae on-edge developed but epitaxial growth did not occur.Epitaxial growth of lamellae between mica could be obtained
however
by confined thin film solution polymerization
with both of the latter samples yielding apparently related ED patterns from a different unit cell than phase I or II.Fiber patterns
obtained from sheared samples
indicated considerably greater crystal disorder than in the nascent crystals.Refinement of the phase I unit cell parameters
based on the [001] and [011] ED patterns
with modeling based on Cerius2
suggests a monoclinic phase I unit cell with α=7.76
b=5.71
c=14.99A
α=γ=90°
β=99.7°
ρ=1.47 g/cm3
space group P121/a1.
Abstract
Confined thin film melt polymerization (CTFMP) of naphthalene chloride/hydroquinone (NCMQ
1/1
molar)mixtures at polymerization temperatures (Tp) below ca. 300℃ resulted in relatively thick
elongated crystals. Polymerizationof NC/HQ above 300℃ between glass yielded well-formed lamellar crystals ca. 100 A thick. Phase Ⅰ and Ⅱ [001] EDpatterns were obtained for all Tp
the relative amount of phase Ⅰ increasing with Tp. Polymerization of naphthalenedicarboxylic acid/hydroquinione diacetate 1/1 mixtures at high Tp also yielded lamellar crystals that "curled up" off of the substrate.When the high temperature CTFMP polymerization was conducted between mica
aggregates of lamellae on-edge developed but epitaxial growth did not occur.Epitaxial growth of lamellae between mica could be obtained
however
by confined thin film solution polymerization
with both of the latter samples yielding apparently related ED patterns from a different unit cell than phase I or II.Fiber patterns
obtained from sheared samples
indicated considerably greater crystal disorder than in the nascent crystals.Refinement of the phase I unit cell parameters
based on the [001] and [011] ED patterns
with modeling based on Cerius2
suggests a monoclinic phase I unit cell with α=7.76
b=5.71
c=14.99A
α=γ=90°
β=99.7°
ρ=1.47 g/cm3
space group P121/a1.
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