Hostname: page-component-6bf8c574d5-gr6zb Total loading time: 0 Render date: 2025-02-22T23:03:09.982Z Has data issue: false hasContentIssue false

Crystallization Processes In Poly (Ethylene Terephthalate) /Polycarbonate Blends

Published online by Cambridge University Press:  15 February 2011

Veronika E. Reinsch
Affiliation:
TRI/Princeton, and Department of Chemical Engineering, Princeton University, P.O. Box 625, Princeton, NJ 08542.
Ludwig Rebenfeld
Affiliation:
TRI/Princeton, and Department of Chemical Engineering, Princeton University, P.O. Box 625, Princeton, NJ 08542.
Get access

Abstract

Blends of poly (ethylene terephthalate), or PET, and polycarbonate (PC) overa range of compositions were studied in isothermal crystallizations from themelt using differential scanning calorimetry (DSC). Both crystallizationrate and degree of crystallinity of PET depend on blend composition. Theglass transition temperature, Tg, of PET and PC in blends andpure polymer were also measured by DSC. Elevation of the Tg ofPET and depression of the Tg of PC are observed upon blending. Incooling scans, dynamic crystallization from the melt was observed. In PET/PCblends with high PC content, a novel dual-peak crystallization of PET wasobserved. The effects of thermal history on crystallization kinetics anddegree of crystallinity were also determined in isothermal crystallizationstudies. For Melt processing times between 1 and 30 Min and for processingtemperatures between 280 and 300 °C, Melt processing temperature was seen tohave a stronger effect than processing time.

Type
Research Article
Copyright
Copyright © Materials Research Society 1994

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

1. Hanrahan, B.D., Angeli, S.R., and Runt, J., Polym. Bull., 15, 455 (1986).Google Scholar
2. Huang, Z.H. and Wang, L.H., Makromol. Chem., Rapid Commun., 7, 255 (1986).Google Scholar
3. Porter, R.S. and Wang, L.-H., Polymer, 33, 2019 (1992).Google Scholar
4. Suzuki, T., Tanaka, H., Nishi, T., Polymer, 30, 1287 (1989).Google Scholar
5. Murff, S.R., Barlow, J.W., and Paul, D.R., J. Appl. Polym. Sci., 29, 3231 (1984).Google Scholar
6. Nadkarni, V.M., Shingankuli, V.L. and Jog, J.P., J. Appl. Polym. Sci., 46, 339 (1992).Google Scholar
7. Martuscelli, E., Polym. Eng. Sci., 24, 563 (1984).Google Scholar
8. Chen, X.-Y. and Birley, A.W., British Polym J., 17, 347 (1985).Google Scholar
9. Birley, A.W. and Chen, X.-Y., Briüsh Polym J., 16, 77 (1984).Google Scholar
10. Menta, A., Gaur, U., Wunderlich, B., J. Polym. Sci., Polym. Phys. Ed., 16, 289 (1978).Google Scholar