Hostname: page-component-848d4c4894-nmvwc Total loading time: 0 Render date: 2024-06-25T05:49:12.914Z Has data issue: false hasContentIssue false

Dynamics of Crystalline and Amorphous Polytetrafluoroethylene Studied by Multiple Quantum NMR

Published online by Cambridge University Press:  15 February 2011

David A. Lathrop
Affiliation:
Department of Chemical Engineering, MIT, Cambridge, MA 02139.
Karen K. Gleason
Affiliation:
Department of Chemical Engineering, MIT, Cambridge, MA 02139.
Get access

Abstract

We report a new technique for probing polymer dynamics through the refocussing of multiple quantum (MQ) nuclear magnetic resonance (NMR) coherences. The MQ-NMR experiment follows the correlated behavior of multiple spin-1/2 nuclei interacting through dipolar couplings. Motion which modulates the dipolar coupling strengths on the same time scale as the experiment (∼1 to 20 kHz) alters the intensity of the observed coherences. Temperature dependent 19F data are presented on polytetrafluoroethylene samples of varying crystallinity. For the as-polymerized 98% crystalline PTFE sample, a sharp increase in MQ coherence refocussing occurs, centered at -298 K. The 64% crystalline melt-quenched sample shows a increase at the same temperature but which has a lower intensity. Thus, the ∼298 K peak is most associated with motion in the crystalline phase. This temperature is intermediate between the two first order transition at 293 and 303 K. Oscillations in the refocussed fractions are observed from 208 to 230 K for the 98% crystalline sample, while this ratio is constant over the same temperature range for the 64% crystalline sample. These oscillations may be associated with paracrystalline defects found only in the first sample. Thus, the MQ refocussing experiment is able to clearly differentiate between polymer samples which have different thermal histories. The sharpness of the MQ refocussing features and their variations in magnitude, shape, and sign with temperature are signatures of the molecular level details of the underlying dynamics which produce them.

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. Yen, Y. and Pines, A., J. Chem. Phys. 78, 3579 (1983).Google Scholar
2. Bunn, C. W. and Howells, E. R., Nature 174, 549 (1954).Google Scholar
3. Clark, E.S. and Muus, L.T., Z. Kristallogr Kristallgeo M. Kristallphys. 117, 119 (1962).Google Scholar
4. Lau, S.F., Suzuki, H., and Wunderlinch, B., J. Polym. Sci., Polym. Phys. Ed. 22, 379 (1984).Google Scholar
5. Eby, R.K. and Sinnott, K.M., J. Appl. Phys. 32, 1765 (1961).Google Scholar
6. Vega, A.J. and English, A.D., Macromolecules 13, 1635 (1980).Google Scholar
7. McCall, D.W., Douglass, D.C., and Falcone, D.R., J. Phys. Chem. 71, 998 (1967).Google Scholar
8. Takenaga, M., Obori, H., and Yamagata, K., J. Polym. Sci. Polym. Lett. Ed. 23, 45 (1985).Google Scholar
9. Ohzawa, Y. and Wada, Y., Japan. J. Appl. Phys. 3, 436 (1964).Google Scholar
10. Krum, F. and Müller, F., Kolloid Z. 164, 81 (1959).Google Scholar
11. McCrum, N.G., Read, B.E., and Williams, G., Analastic and Dielectric Effects in Polymer Solids (Wiley, New York, 1967).Google Scholar
12. Wada, Y. and Hayakawa, R., in Progress in Polymer Science. Japan, edited by Okamura, and Takayanagi, , (Kodansha, Tokyo, 1972), Vol. 3.Google Scholar
13. Starkweather, H., Zoller, P., Jones, G., and Vega, A., J. Polym. Sci. Polym. Phys. Ed. 20, 751 (1982).Google Scholar
14. Takenaga, M., Yamagata, K., Kasai, A., and Ariyama, T., J. Appl. Polym. Sci. 39, 1689 (1990).Google Scholar