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Phase Separation Kinetics During Drying

Published online by Cambridge University Press:  10 February 2011

R. F. Saraf
Affiliation:
IBM Corp., T.J.Watson Research Center, Yorktown Hts., NY 10598
S. Ostrander
Affiliation:
Dept. of Material Sci., Alfred University, Alfred, NY 14802
R. M. Feenstra
Affiliation:
Physics Dept., Carnegie Mellon University, Pittsburgh, PA 15213
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Abstract

Kinetics of phase separation at air/polymer interface in a binary polymer mixture on evaporation of common solvent is studied. The lateral dimension of the highly anisotropie, pancake-like, minority phase increases with a growth exponent of 2/3 identical to ‘late-stage’ growth under (classical) thermal-quench at interface. In contrast to the thermal-quench, during drying the kinetics depends on the initial condition (i.e., initial concentration, Co) that is rescaled to obtain a master-curve.

Type
Research Article
Copyright
Copyright © Materials Research Society 1997

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References

(1) Guenoun, P., Beysens, D., Robert, M., Phys. Rev. Lett., 1990, 65 2406.Google Scholar
(2) Wiltzius, P., Cumming, A., Phys. Rev. Lett., 1991, 66, 3000.Google Scholar
(3) Jones, R.A.L., Norton, L.J., Kramer, E.J., Bates, F.S., Wiltzius, P., Phys. Rev. Lett. 1991, 66 1326.Google Scholar
(4) Bruder, F., Brenn, R., Phys. Rev. Lett., 1992, 69, 624.Google Scholar
(5) Tanaka, H., Phys. Rev. Lett., 1993, 70, 2770.Google Scholar
(6) Tanaka, H., Phys. Rev. Lett., 1993, 70, 53.Google Scholar
(7) Siggia, E.D., Phys. Rev. A, 1979, 20, 595.Google Scholar
(8) Chan, J.W., J. Chem. Phys., 1977, 66, 3667.Google Scholar
(9) Shi, B.Q., Harrison, C, Cumming, A., Phys. Rev. Lett, 1993, 70, 206.Google Scholar
(10) Saraf, R.F., Macromolecules, (1993), 26, 36.Google Scholar
(11) Brenker, M.J., Feger, C, J. Polym. Sci., Polym. Chem. Ed., 1987, 25, 2005.Google Scholar
(12) Stoffel, N.C., Kramer, E.J., Volkeson, W., Russell, T.P., Polymer, 1993, 34, 4524.Google Scholar
(13) The reported diffusion constant of water in PMDA-ODA polyimide film is ∼5×10∼−9 cm2/sec. (Li, S.Z., Pak, Y.S., Adamie, K., Greenbaum, S.G., Lim, B.S., Xu, B., Xu, G., Nowick, A.S., J Electrochem. Soc., 1992, 139, 662) at room temperature. Since size of NMP molecule is larger than water, D > 10−9 cm2/sec. However, the films in these studies are not cured to rigid polyimide structure. Thus, conservatively, at 70 °C, we assume D ∼ 10'−9 cm2/sec. (at most).+10−9+cm2/sec.+However,+the+films+in+these+studies+are+not+cured+to+rigid+polyimide+structure.+Thus,+conservatively,+at+70+°C,+we+assume+D+∼+10'−9+cm2/sec.+(at+most).>Google Scholar
(14) Crank, J., The Mathematics of Diffusion, 2nd ed., Oxford University Press, Oxford (1975), p. 50, Fig. 4.1.Google Scholar
(15) Saraf, R.F., Feenstra, R.M., Ostrander, S., Langmuir, submitted.Google Scholar