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Polarized FT‐IR photoacoustic spectroscopy on polymer fibers
Author(s) -
Eichhorn KlausJochen,
Adam Gudrun
Publication year - 2004
Publication title -
macromolecular symposia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.257
H-Index - 76
eISSN - 1521-3900
pISSN - 1022-1360
DOI - 10.1002/masy.200450110
Subject(s) - materials science , polymer , polyurethane , photoacoustic spectroscopy , elastomer , fiber , spinning , orientation (vector space) , amorphous solid , photoacoustic imaging in biomedicine , infrared spectroscopy , composite material , spectroscopy , infrared , optics , crystallography , chemistry , organic chemistry , physics , geometry , mathematics , quantum mechanics
The orientation of macromolecular chains in two melt‐spun polymer fibers (segmented polyurethane elastomer and melt‐modified polyolefine fibers) was studied by photoacoustic spectroscopy (PAS) with polarized light in the mid‐infrared range. The PAS orientation functions calculated from the photoacoustic signal intensities of orientation sensitive bands describe the orientation of the different chain segments with respect to the fiber axis. Thus, the orientation of hard and soft segments in the unstressed polyurethane fiber is different and both are similiar to that of the corresponding injection molded bars. With increased spinning velocity an improved orientation of the polyolefine chains along the fiber axis, but only in the amorphous regions of the polymer, were detected. Only a slight reduction of orientation was measured as a result of the subsequent chemical crosslinking in the polyolefines.