Hostname: page-component-cd9895bd7-jkksz Total loading time: 0 Render date: 2024-12-27T02:23:35.605Z Has data issue: false hasContentIssue false
  • English
  • Français

Dynamic IR Studies of Microdomain Interphases of Isotope-Labeled Block Copolymers

Published online by Cambridge University Press:  21 February 2011

I. Noda ,
S. D. Smith ,
A. E. Downey ,
J. T. Grothaus  and
C. Marcott
I. Noda
Affiliation:
The Procter & Gamble Company, Miami Valley Laboratories, P.O. Box 398707, Cincinnati, OH 45239-8707
S. D. Smith
Affiliation:
The Procter & Gamble Company, Miami Valley Laboratories, P.O. Box 398707, Cincinnati, OH 45239-8707
A. E. Downey
Affiliation:
The Procter & Gamble Company, Miami Valley Laboratories, P.O. Box 398707, Cincinnati, OH 45239-8707
J. T. Grothaus
Affiliation:
The Procter & Gamble Company, Miami Valley Laboratories, P.O. Box 398707, Cincinnati, OH 45239-8707
C. Marcott
Affiliation:
The Procter & Gamble Company, Miami Valley Laboratories, P.O. Box 398707, Cincinnati, OH 45239-8707
Get access

Abstract

By probing the localized segmental motion of isotope-labeled block copolymers, the physical nature of the interphase region between microphaseseparated domains of block polymers was examined. Dynamic infrared linear dichroism (DIRLD) spectroscopy, which measures the reorientations of submolecular structures induced by a small-amplitude oscillatory strain, was combined with specific isotope-labeling using deuterium-substituted monomers. The latter technique enabled us to differentiate the dynamic responses of well-defined parts of block segments, e.g., near the segment junction, chain end, or middle of the block. The degree of segmental interactions near the interphase region of styrene-isoprene diblock copolymers were studied as a function of the segment location and temperature. The reorientational motion of the polystyrene segment, especially near the block junction, was monitored around the glass transition temperature of the polyisoprene matrix. From this result, the degree of segmental mixing in the interphase region which leads to local plasticization of the polystyrene segment was determined.

Type
Research Article
Information
MRS Online Proceedings Library (OPL) , Volume 171: Symposium O – Polymer Based Molecular Composites , 1989 , 117
Copyright
Copyright © Materials Research Society 1990

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. Learry, D.F. and Williams, M.C., J. Polym. Sci., Polym. Phys. Ed. 12, 265 (1974).Google Scholar
2. Meier, D., J. Polym. Sci., Part C 26, 81 (1969).Google Scholar
3. Helfand, E. and Wasserman, Z.R., Macromolecules 9, 879 (1976).Google Scholar
4. Ruland, W., J. Appl. Crystallogr. 13, 34 (1971).Google Scholar
5. Hashimoto, T., Fujimura, M., and Kawai, H., Macromolecules 13, 1660 (1980).Google Scholar
6. Kraus, G. and Rollman, K.W., J. Polym. Sci., Polym. Phys. Ed. 14, 1133 (1976).Google Scholar
7. Ruland, W., Macromolecules 20, 87 (1987).Google Scholar
8. Gronski, W. and Stöppelmann, G., Polym. Prepr. 29 (1), 46 (1988).Google Scholar
9. Noda, I., Dowrey, A.E., and Marcott, C., in Fourier Transform Infrared Characterization of Polymers, edited by Ishida, H. (Plenum, New York, 1987), pp. 33–59.Google Scholar
10. Noda, I., Dowrey, A.E., and Marcott, C., Appl. Spectrosc. 42, 203 (1988).Google Scholar
11. Hoover, J.M. and McGrath, J.E., Polym. Prepr. 27 (2), 150 (1986).Google Scholar