1998
DOI: 10.1002/(sici)1521-3935(19980201)199:2<215::aid-macp215>3.0.co;2-t
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Sequential reordering in condensation copolymers, 4. Crystallization-induced sequential reordering in poly(ethylene terephthalate)/polycarbonate copolymers as revealed by the behavior of the amorphous phases

Abstract: SUMMARY An equimolar blend of poly(ethy1ene terephthalate) (PET)' and bisphenol-A-polycarbonate (PC)d is studied by dynamic-mechanical thermal analysis (DMTA) and X-ray scattering after thermal treatment that enables transesterification. As demonstrated by wide-angle X-ray scattering (WAXS) measurements, prolonged thermal treatment at 280°C gives rise to a copolymer that no longer reveals melting or crystallization. In accordance with previous reports, this effect is attributed to the formation of a random cop… Show more

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Cited by 20 publications
(11 citation statements)
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“…This leads to a lower degree of crystallinity at usual under cooling for the finest degree of dispersion and complex melting patterns in DSC 44. This could explain the dual crystallization exotherms observed during the dynamic crystallization from the melt of blends with a high content of PC (typically more than 60%) reported by Reinsch et al45 The authors attributed the normal exotherm at roughly 210 °C to normal PET crystallization while the low temperature exotherm was attributed to a co‐crystalline form of PET‐PC or a different crystalline structure.…”
Section: Introductionmentioning
confidence: 94%
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“…This leads to a lower degree of crystallinity at usual under cooling for the finest degree of dispersion and complex melting patterns in DSC 44. This could explain the dual crystallization exotherms observed during the dynamic crystallization from the melt of blends with a high content of PC (typically more than 60%) reported by Reinsch et al45 The authors attributed the normal exotherm at roughly 210 °C to normal PET crystallization while the low temperature exotherm was attributed to a co‐crystalline form of PET‐PC or a different crystalline structure.…”
Section: Introductionmentioning
confidence: 94%
“…Finally, though long residence times in the melt give rise to exchange reaction and generate block copolymers of PET and PC, followed by a randomization, restoring of block copolymers from truly amorphous random PET‐PC copolymers by annealing at 235 °C, called crystallization induced sequential reordering, have been mentioned 45…”
Section: Introductionmentioning
confidence: 99%
“…With the PET/PC system, the DSC method and instrumentation used allowed us to follow the behaviour of the amorphous phases as a function of the crystallinity changes only in the blend compositions with predominant concentrations of the non-crystallisable component (Figure 11A). Therefore, the changes in Tg values with the progress of transreactions in the PET/PC system were followed, using a more sensitive technique (DMTA), in order to get further evidence for the direction of these transreactions in the system under investigation [80]. Therefore, the changes in Tg values with the progress of transreactions in the PET/PC system were followed, using a more sensitive technique (DMTA), in order to get further evidence for the direction of these transreactions in the system under investigation [80].…”
Section: Evidence Of Crystallisation-induced Reorderkg Derived Fiommentioning
confidence: 99%
“…Temperature dependences of the loss modulus El' (in bending mode) for neat homopolymers, their equimolar mixture, and copolymers with different sequential order: (a) neat PET; (b) neat PC; (c) mechanical mixture; (d) block copolymer;(e) randomised sample; (f) restored block copolymer[80] …”
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confidence: 99%
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