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Unique orientation of lamellae in film processed poly (phenylene sulfide)
Author(s) -
Huo Peter Pengtao,
Chung Jerry Sengshiu,
Cebe Peggy
Publication year - 1992
Publication title -
polymer composites
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.577
H-Index - 82
eISSN - 1548-0569
pISSN - 0272-8397
DOI - 10.1002/pc.750130503
Subject(s) - materials science , crystallinity , amorphous solid , differential scanning calorimetry , composite material , glass transition , scanning electron microscope , phase (matter) , phenylene , crystallography , polymer , thermodynamics , chemistry , physics , organic chemistry
The morphology of poly(phenylene sulfide), PPS, obtained as processed film has been studied using wide angle X‐ray scattering (WAXS), scanning electron microscopy (SEM), and differential scanning calorimetry (DSC). A unique morphology has been identified in the original film. The spherulites are very small in size and possess a cylindrical symmetry with their lamellae oriented on the edge. In these processed PPS films, the a ‐axis of the lattice is preferentially aligned perpendicular to the film plane, while the b and c axes are predominantly in the film plane. In the PPS isothermally crystallized from the melted, original film, there is no such preferential orientation. Thermal analysis of the original and melt crystal‐lized PPS shows that while the degree of crystallinity is about the same, the nature of the amorphous phase in the two materials is different. In the original film, we did not observe a heat capacity increment at a glass transition temperature by DSC, indicating that all of the amorphous phase belongs to the category of rigid amorphous phase. In the melt crystallized PPS, a distinct glass transition was seen, though only a portion of the amorphous phase becomes mobile at T g . The differences in orientation and mobility of the amorphous phase in the original film compared to melt crystallized PPS are explained by the different thermal processing procedures used for the two materials.

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