Hostname: page-component-8448b6f56d-xtgtn Total loading time: 0 Render date: 2024-04-19T05:18:31.351Z Has data issue: false hasContentIssue false

Carbon-13 Two Dimensional Chemical Shift Anisotropy Exchange Patterns in Blends of Polyphenylene Oxide and Polystyrene Near the Glass Transition

Published online by Cambridge University Press:  16 February 2011

P. T. Inglefield
Affiliation:
Department of Chemistry, Clark University, Worcester, MA01610.
A. A. Jones
Affiliation:
Department of Chemistry, Clark University, Worcester, MA01610.
P. Wang
Affiliation:
Department of Chemistry, Clark University, Worcester, MA01610.
C. Zhang
Affiliation:
Department of Chemistry, Clark University, Worcester, MA01610.
Get access

Abstract

Two dimensional solid state NMR exchange spectroscopy can be used to monitor slow motions on time scales comparable to dynamical mechanical spectroscopy. Polyphenylene oxide, carbon-13 labeled in a methyl position, was blended with polystyrene. The resulting compatible blends have single thermal glass transitions (Tg) at temperatures between those of the homopolymers. The chemical shift anisotropy line shape of the labeled methyl shows reorientational exchange at temperatures near the thermal glass transition. The 2D exchange pattern contains information on the rate and amplitude of the motion. The data indicate Brownian rotational angular diffusion of the phenylene oxide units with rates in the millisecond to second range. The motional description associated with the glass transition is contrasted with those appropriate to single component polymeric glasses. It is concluded that in the blend system the onset of motion occurs at a lower temperature relative to the DSC Tg than in the homopolymer and there is evidence for considerably more dynamic heterogeneity.

Type
Research Article
Copyright
Copyright © Materials Research Society 1991

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

1. Hay, A.S., Polym.Eng.Sci., 16,(1),1 (1976).Google Scholar
2. Paul, D.R. and Newman, S., “Polymer Blends”, Academic Press (1977)Google Scholar
3. Shultz, A.R. and Gendron, B.M., J. Appl. Polym. Sci., 16, 461(1972)Google Scholar
4. Wang, L.H. and Porter, R.S.,J. Polym. Sci. Polym. Phys.Ed., 21, 907(1983)Google Scholar
5. Stoelting, J., Karas, F.E. and MacKnight, W.J., Polym. Eng. Sci., 10, 133(1970)Google Scholar
6. Yee, A.F., Polymer Preprints, ACS,17, (1),145(1976)Google Scholar
7. Shultz, A.R. and Beach, B.M., Macromolecules, 7, 902(1974)CrossRefGoogle Scholar
8. MacKnight, W.J., Stoelting, J., Karas, F.E., Adv. Chem. Ser.,99,29(1971)Google Scholar
9. Caravatti, P., Bodenhausen, G. and Ernst, R.R., J. Magn. Res.,55,88(1988)Google Scholar
10. Bronniman, C.E., Szeverenyi, N.M. and Maciel, G.E., J. Chem. Phys., 79, 3694 (1983)Google Scholar
11. Linder, M., Henrichs, P.M., Hewitt, J.M. and Massa, D.J., J. Chem. Phys., A82,1585 (1985)Google Scholar
12. Roy, A.K., Inglefield, P.T., Shibata, J.H. and Jones, A.A., Macromolecules,20,1434 (1987)CrossRefGoogle Scholar
13. Wang, P., Jones, A.A., Inglefield, P.T., White, D.M. and Bendler, J.T., New Polymeric Mater., 2, to appear.Google Scholar
14. Belfiore, L.A., Henrichs, P.M., Massa, D.J., Zumbulyadis, N.,Rothwell, W.P. and Cooper, S.L., Macromolecules, 16,1744(1983)Google Scholar
15. Wehrle, M., Hellmann, G.P. and Spiess, H.W., Coll. and Polym. Sci., 265,815(1987)Google Scholar
16. Liu, Y., Roy, A.K., Jones, A.A., Inglefield, P.T. and Ogden, P., Macromolecules, 23, 968(1990)CrossRefGoogle Scholar
17. Schmidt, C., Blumich, B. and Spiess, H.W., J.Mag.Res., 79, 269(1988)Google Scholar
18. Wefing, S. and Spiess, H.W., J. Chem. Phys.,89,1219(1988)Google Scholar
19. Wefing, S., Kaufmann, S. and Spiess, H.W., J. Chem. Phys.,89,1234(1988)Google Scholar
20. Kaufman, S.,Wefing, S.,Schaefer, D. and Spiess, H.W., J. Chem. Phys., 93,197(1990)Google Scholar
21. States, D.J., Habekorn, R.A. and Ruben, D.J., J. Mag. Res.,48,286(1982)Google Scholar
22. Williams, M.,Landel, R.J. and Ferry, J.D., J.Am.Chem.Soc.,77,3701(1955)Google Scholar