Hostname: page-component-586b7cd67f-t7czq Total loading time: 0 Render date: 2024-11-26T09:21:16.586Z Has data issue: false hasContentIssue false

Wetting on Grafted Polymer Films

Published online by Cambridge University Press:  29 November 2013

Get access

Extract

Studying the properties of endanchored polymer layers has been a fashionable occupation for numerous physicists, chemists, and material scientists for more than 10 years. Theoreticians have realized that grafted macromolecules are nice statistical objects wriggling around under thermal motion, which give rise to nontrivial long-range entropic effects. These can be described by elegant scaling laws and analogies with quantum or classical mechanics. For experimenters the area turned out to be a marvelous playground in which both very simple and sophisticated techniques such as x-ray or neutron scattering and reflectivity, nuclear magnetic resonance (NMR), Rutherford backscattering, and optical and atomic force microscopy (AFM) have been used to discover interesting and subtle phenomena. All this effort was also motivated by the importance of grafted layers in applications such as paints, adhesives, lubricants, colloidal stabilizers, and composite materials. By anchoring a thin, soft polymer layer to a solid surface, one can tune the surface properties. In this short article, we will discuss how the wetting and spreading of liquids and polymer melts can be profoundly altered by the presence of such protective layers.

Type
Theory and Simulation of Polymers at Interfaces
Copyright
Copyright © Materials Research Society 1997

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.de Gennes, P.G., Macromolecules 13 (1980) p. 1069.CrossRefGoogle Scholar
2.Milner, S.T., Science 251 (1991) p. 845.CrossRefGoogle Scholar
3.Semenov, A.N., Sov. Phys. JETP 61 (1985) p. 733.Google Scholar
4.Mourran, A., PhD dissertation, Université Pierre et Marie Curie Paris VI, 1995.Google Scholar
5.Leibler, L., Ajdari, A., Mourran, A., Coulon, G., and Chatenay, D. in Ordering in Macromolecular Systems (Springer Verlag, Berlin, 1994) p. 301.CrossRefGoogle Scholar
6.Shull, K.R., Faraday Soc. Discuss. 98 (1994) p. 203.CrossRefGoogle Scholar
7.Witten, T., Leibler, L., and Pincus, P., Macromolecules 23 (1990) p. 824.CrossRefGoogle Scholar
8.Liu, Y., Rafailovich, M.H., Sokolov, J., Schwarz, S.A., Zhong, X., Eisenberg, A., Kramer, E.J., Sauer, B.B., and Satija, S., Phys. Rev. Lett. 73 (1994) p. 140.Google Scholar
9.Reiter, G., Schultz, J., Auroy, P., and Auvray, L., Europhys. Lett. 33 (1996) p. 29.CrossRefGoogle Scholar
10.Henn, G., Bucknall, D.G., Stamm, M., Vanhoorne, P., and Jérôme, R., Macromolecules 29 (1996) p. 4305.CrossRefGoogle Scholar
11.Hare, E.F. and Zisman, W.A., J. Phys. Chem. 59 (1955) p. 335.CrossRefGoogle Scholar
12.Gast, A. and Leibler, L., Macromolecules 19 (1986) p. 686.CrossRefGoogle Scholar
13.Mourran, A.et al. (unpublished).Google Scholar
14.Fredrickson, G.H., Ajdari, A., Leibler, L., and Carton, J.P., Macromolecules 25 (1992) p. 2882.CrossRefGoogle Scholar
15.Long, D., Ajdari, A., and Leibler, L., Langmuir 12 (1996) p. 1675.CrossRefGoogle Scholar
16.de Gennes, P.G., Rev. Mod. Phys. 57 (1985) p. 825.CrossRefGoogle Scholar
17.Carré, A. and Shanahan, M.E.R., Langmuir 11 (1995) p. 24.CrossRefGoogle Scholar