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Effect of high‐performance polymers on crystallization and multiple melting behavior of poly(phenylene sulfide)
Author(s) -
Mai Kancheng,
Mei Zhen,
Xu Jiajui,
Zeng Hanmin
Publication year - 1998
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/(sici)1097-4628(19980725)69:4<637::aid-app2>3.0.co;2-k
Subject(s) - peek , materials science , crystallization , differential scanning calorimetry , phenylene , polysulfone , polymer chemistry , thermoplastic , sulfide , phenolphthalein , composite material , ether , amorphous solid , polymer blend , polyether ether ketone , miscibility , polymer , chemical engineering , copolymer , organic chemistry , chemistry , physics , thermodynamics , engineering , metallurgy
The crystallization and multiple melting behavior of poly(phenylene sulfide) (PPS) and its blends with amorphous thermoplastic bisphenol A polysulfone (PSF) and phenolphthalein poly(ether ketone) (PEK‐C), crystalline thermoplastic poly(ether ether ketone) (PEEK), and thermosetting bismaleimide (BMI) resin were investigated by a differential scanning calorimeter (DSC). The addition of PSF and PEK‐C was found to have no influence on the crystallization temperature ( T c ) and heat of crystallization (Δ H c ) of PPS. A significant increase in the value of T c and the intensity of the T c peak of PPS was observed and the crystallization of PPS can be accelerated in the presence of the PEEK component. An increase in the T c of PPS can also be accelerated in the BMI/PPS blend, but was no more significant than that in the PEEK/PPS blend. The T c of PPS in the PEEK/PPS blends is dependent on the maximum temperature of the heating scans and can be divided into three temperature regions. The addition of a second component has no influence on the formation of a multiple melting peak. The double melting peaks can also be observed when PPS and its blends are crystallized dynamically from the molten state. © 1998 John Wiley & Sons, Inc. J Appl Polym Sci 69: 637–644, 1998

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