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11. |
Kinetics of microstructure rearrangement during annealing of cold‐drawn isotactic polypropylene |
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Journal of Polymer Science: Polymer Physics Edition,
Volume 20,
Issue 3,
1982,
Page 497-508
Suzanne Babajko,
J. M. Schultz,
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摘要:
AbstractThe microstructure of polypropylene, annealed after cold drawing to an oriented state, was examined using density measurements and small‐ and wide‐angle x‐ray scattering (SAXS and WAXS) techniques. SAXS patterns were obtained after annealing (in an oil bath), and during annealing (of samples annealed in a furnace placed directly in the x‐ray beam). Data, for isothermal annealing, showed an increase in SAXS intensity, in crystal perfection, and in density over the observed time range, but no change in long spacing during the same period. Long spacing, SAXS intensity, and density were all strongly dependent upon annealing temperature, increasing at higher temperatures. Upon annealing the elastic modulus and yield strength dropped below the as‐drawn values in an immeasurably short time, and did not appear to change thereafter during the time range examined. The decrease was more marked for higher‐temperature annealing. The kinetics of the micro‐structural changes are compared qualitatively to the predictions of nucleation and growth theory and of spinodal decomposition. The defects in the microstructure are considered as the “solute molecules” of the spinodal model. The experimental results do not agree neatly with either model. However, a nonequilibrium thermodynamic approach appears to be the more promising. It is suggested that the kinetics of mechanical property change may be due to different rates of migration for differe
ISSN:0098-1273
DOI:10.1002/pol.1982.180200311
出版商:John Wiley&Sons, Inc.
年代:1982
数据来源: WILEY
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12. |
Spectroscopic study of rigid‐rod polymers. II. Protonation effect |
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Journal of Polymer Science: Polymer Physics Edition,
Volume 20,
Issue 3,
1982,
Page 509-521
D. Y. Shen,
G. M. Venkatesh,
D. J. Burchell,
P. H. C. Shu,
S. L. Hsu,
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摘要:
AbstractThe protonation of a heterocyclic rigid‐rod polymer poly(p‐phenylene benzbisthiazole) and its model compound has been studied by UV‐visible and Raman spectroscopy. Because of the two nitrogens on the heterocyclic ring, spectroscopic features of unprotonated, half‐protonated, and fully protonated structures have been identified. For the fully protonated molecule, there is also an increase in conjugation between the phenyl ring and the heterocycl
ISSN:0098-1273
DOI:10.1002/pol.1982.180200312
出版商:John Wiley&Sons, Inc.
年代:1982
数据来源: WILEY
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13. |
The kinetics of defect clustering in fibrillar polypropylene crystals |
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Journal of Polymer Science: Polymer Physics Edition,
Volume 20,
Issue 3,
1982,
Page 523-534
J. Petermann,
R. M. Gohil,
J. M. Schultz,
R. W. Hendricks,
J. S. Lin,
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摘要:
AbstractPolypropylene films were produced by solidification during high‐rate (>104s−1) melt drawing. Small‐angle x‐ray scattering (SAXS) data were collected during interruptions of the annealing of these films. Fibrillar crystallization took place during the melt‐drawing process. The fibrils exhibit an axial density modulation as determined by SAXS and transmission electron microscopy. Annealing increases the amplitude of the density modulation. Detailed examination of the SAXS curves shows that the modulation is approximately sinusoidal and that the amplification of the density modulation occurs with no change in periodicity. Comparison of SAXS curves taken at different times during annealing suggests a process similar to spinodal decomposition. It is proposed that the microstructural change within a fibril takes place by the axial motion and clustering of chai
ISSN:0098-1273
DOI:10.1002/pol.1982.180200313
出版商:John Wiley&Sons, Inc.
年代:1982
数据来源: WILEY
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14. |
The crystal structure of the alternating copolymer of hexafluoroisobutylene and vinylidene fluoride |
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Journal of Polymer Science: Polymer Physics Edition,
Volume 20,
Issue 3,
1982,
Page 535-552
S. Weinhold,
M. H. Litt,
J. B. Lando,
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摘要:
AbstractThe crystal structure of the alternating copolymer of hexafluoroisobutylene and vinylidene fluoride, P(HFIB/VF2), was determined usingx‐ray diffraction techniques. Oriented specimens of the copolymer were produced by drawing melt‐pressed film at 300°C. The unit cell of P(HFIB/VF2) is orthorhombic with dimensions ata= 1.064,b= 1.837, and c = 0.783 nm. The chain conformation is a 21helix with an approximatetrans‐trans‐gauche‐gauchebackbone dihedral‐angle sequence. Severe intrachain steric crowding exists; as a consequence, the chain is quite rigid and some of the backbone bond angles are highly extended. The unit cell contains four such chains packed according to the symmetry of space group Iba2. Neighboring chains in a crystal are mechanically interlocked; in combination with the rigidity of the chains, this is the basis for the superior mechanical properties of the copolymer compared to PTFE. A structure containing up to 20‐30% of head‐to‐head residues was found to be statistically indistinguishable from a completely head
ISSN:0098-1273
DOI:10.1002/pol.1982.180200314
出版商:John Wiley&Sons, Inc.
年代:1982
数据来源: WILEY
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15. |
IR studies of the deuteration of polyacrylamide |
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Journal of Polymer Science: Polymer Physics Edition,
Volume 20,
Issue 3,
1982,
Page 553-556
W.‐M. Kulicke,
H. W. Siesler,
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ISSN:0098-1273
DOI:10.1002/pol.1982.180200315
出版商:John Wiley&Sons, Inc.
年代:1982
数据来源: WILEY
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16. |
Increased water sorption of poly(methyl methacrylate) after removal of methanol |
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Journal of Polymer Science: Polymer Physics Edition,
Volume 20,
Issue 3,
1982,
Page 557-560
E. E. LaBarre,
D. T. Turner,
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ISSN:0098-1273
DOI:10.1002/pol.1982.180200316
出版商:John Wiley&Sons, Inc.
年代:1982
数据来源: WILEY
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