Hostname: page-component-cd9895bd7-lnqnp Total loading time: 0 Render date: 2024-12-27T01:58:59.926Z Has data issue: false hasContentIssue false

NMR Studies of Solvent Dynamics in High Solids Alumina Slurries

Published online by Cambridge University Press:  15 February 2011

Anthony A. Parker
Affiliation:
Aluminum Company of America, Alcoa Center, PA 15069.
Deborah M. Wilhelmy
Affiliation:
Aluminum Company of America, Alcoa Center, PA 15069.
William Daunch
Affiliation:
Aluminum Company of America, Alcoa Center, PA 15069.
Get access

Abstract

Solid state 13C NMR techniques have been used to study the mobility of both toluene and ethanol in slurries containing 70% alumina by weight. A comparison of relative signal intensities from cross polarization experiments, and from single excitation experiments under static conditions (no sample spinning) shows that a portion of the solvent molecules are immobilized with “solid” characteristics, while a majority of the molecules exist in mobile or “liquid” like environments. The immobilized solvent is rigid enough to cross polarize with protons, and hence it is characterized by long correlation times, and by a high viscosity. The remainder of the solvent is too mobile to cross polarize, and hence it is characterized by a lower viscosity. The results suggest that solvent is partitioned with the most viscous components being bound near the particle surfaces. These experiments and calculations will be discussed along with the implied effects of solvent partitioning on bulk rheological behavior.

Type
Research Article
Copyright
Copyright © Materials Research Society 1993

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. Tadros, T. F., Chemistry and Industry, 1, 210 (1985).Google Scholar
2. Lonnqvist, I., Khan, A., Soderman, O., Journal of Colloid and Interface Science, 144(2), 401 (1991).Google Scholar
3. van der Beek, G. P., et al., Langmuir, 7, 327 (1991).Google Scholar
4. Stejskal, E. O., Schaefer, J., Macromolecules, _14, 275 (1981).Google Scholar
5. Roy, A. K., Inglefield, P. T., Progress in NMR Spectroscopy, 22, 569 (1990).Google Scholar
6. Schaefer, J., Garbow, J. R., Macromolecules, 20, 1271 (1987).Google Scholar
7. Parker, A. A., Hedrick, D. P., Marcinko, J. J., Ritchey, W. M., Polymer Preprints, 33(l), 126 (1992).Google Scholar
8. Belfiore, L. A., Polymer, 21, 80 (1986).Google Scholar
9. Parker, A. A., Marcinko, J. J., Shich, Y. T., Hedrick, D. P., Ritchey, W. M., J. Appl. Polym. Sci., 40, 1717 (1990).Google Scholar
10. Marcinko, J. J., Parker, A. A., Shieh, Y. T., Ritchey, W. M., J. Appl. Polym. Sci., 45, 391 (1992).Google Scholar
11. Parker, A. A., Marcinko, J. J., Rinaldi, P., Hedrick, D. P., Ritchey, W. M., J. Appl. Polym. Sci., in review.Google Scholar
12. Bloembergen, N., Purcell, E. M., Pound, R. V., Physical Review, 73(7), 679 (1948).Google Scholar