Hostname: page-component-586b7cd67f-vdxz6 Total loading time: 0 Render date: 2024-11-25T15:45:10.406Z Has data issue: false hasContentIssue false

Effect of Solvent Quality on the Friction Forces Between Polymer Brushes

Published online by Cambridge University Press:  17 March 2011

Aaron M. Forster
Affiliation:
Department of Chemical EngineeringClemson UniversityClemson, SC 29634
S. Michael Kilbey II
Affiliation:
Department of Chemical EngineeringClemson UniversityClemson, SC 29634
Get access

Abstract

We have used the surface forces apparatus to measure the structural and frictional force profiles between opposing, solvated brush layers as a function of temperature. Two different polyvinylpyridine-polystyrene [PVP-PS] diblock copolymers were used to make PS brushes. The molecular weights (in thousands) of these PVP-PS materials were [114/103]k, [30/70]k, respectively. Structural and frictional force profiles in toluene and cyclohexane were measured, and the cyclohexane experiments were conducted at temperatures ranging from the theta-point to 50°C. In toluene the PS brushes needed to be compressed to ∼1/5th of their equilibrium height before frictional forces were measured, but this onset of frictional forces was detected at a much lower level of compression in near-theta cyclohexane. In cyclohexane the structural force profiles were basically insensitive to the temperature change, but the frictional forces depended strongly on the solvent temperature. When the cyclohexane temperature was raised, the onset of frictional forces decreased toward the good-solvent onset. We also discuss the dependence of frictional force on shearing parameters.

Type
Research Article
Copyright
Copyright © Materials Research Society 2002

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. Alexander, S., J. Phys. (France) 38, 983 (1977).Google Scholar
2. Gennes, P. G. de, Macromolecules 13, 1069 (1980).Google Scholar
3. Milner, S. T., J. Chem. Soc. Faraday Trans. 86, 1349 (1990).Google Scholar
4. Kilbey, S. M., Watanabe, H., Tirrell, M., Macromolecules 34, 5249 (2001).Google Scholar
5. Auroy, P., Mir, Y., Auvray, L., Phys. Rev. Lett. 69, 93 (1992).Google Scholar
6. Watanabe, H., Tirrell, M., Macromolecules, 26, 6455 (1993).Google Scholar
7. Klein, J., Kumacheva, E., Mahalu, D., Perahia, D., Fetters, L. J., Acta. Polym. 49, 617 (1998).Google Scholar
8. Kilbey, S. M. II, Schorr, P., Tirrell, M., in Dynamics of Small Confining Systems IV, edited by Drake, J.M., Grest, G.S., Klafter, J., Kopelman, R., (Mater. Res. Soc. Proc., Pittsburgh, PA 1999).Google Scholar
9. Schorr, P. A., Kwan, T. C. B., Kilbey, S. M. II, Shaqfeh, E. S. G., Tirrell, M., submitted to Macromolecules.Google Scholar
10. Schorr, P. A., Ph.D. thesis, University of Minnesota (2000).Google Scholar
11. Klein, J., Perahia, D., Warburg, S., Nature 353, 143 (1991).Google Scholar
12. Klein, J., Kumacheva, E., Perahia, D., Mahalu, D., Warburg, S., Faraday Discuss. 98, 173 (1994).Google Scholar
13. Granick, S., Demirel, A. L., Cai, L. L., Peanasky, J., J. Chem. (Israel) 35, 75 (1995).Google Scholar
14. Dhinojwala, A., Cai, L., Granick, S., Langmuir 12, 4537 (1996).Google Scholar
15. Grest, G. S., Adv. Poly. Sci. 138, 149 (1999).Google Scholar
16. Karim, A., Satija, S., Douglas, J. G., Ankner, J. F., Fetters, L. J., Phys. Rev. 73, (1994)Google Scholar
17. Kelley, T. W., Schorr, P. A., Johnson, K. D., Tirrell, M., Frisbie, C. D., Macromolecules, 31, (1998), 4297 Google Scholar