Hostname: page-component-8448b6f56d-jr42d Total loading time: 0 Render date: 2024-04-25T01:10:02.958Z Has data issue: false hasContentIssue false

Strengthening Epoxy/High Impact Polystyrene Interfaces Using End Grafting Polymer Chains

Published online by Cambridge University Press:  10 February 2011

Y. Sha
Affiliation:
Theoretical & Applied Mechanics, Cornell University, Ithaca, NY 14853 The Materials Science Center, Cornell University, Ithaca, NY 14853
C. Y. Hui
Affiliation:
Theoretical & Applied Mechanics, Cornell University, Ithaca, NY 14853 The Materials Science Center, Cornell University, Ithaca, NY 14853
E. J. Kramer
Affiliation:
Materials Science and Engineering, Cornell University, Ithaca, NY 14853 The Materials Science Center, Cornell University, Ithaca, NY 14853
S. F. Hahn
Affiliation:
Dow Chemical Co., Central Research and Development, Midland, MI 48674
C. A. Berglund
Affiliation:
Dow Chemical Co., Central Research and Development, Midland, MI 48674
Get access

Abstract

The fracture toughness Gc of epoxy/high impact polystyrene (HIPS) interfaces was measured as a function of grafting chain density Σ of dPS-COOH chains of various degrees of polymerization N. For short chains, no effective entanglements can be formed between the dPS chains and the PS matrix of the HIPS, thus no enhancement in Gc over that of a bare interface. For very long chains, even though each chain is well entangled with the HIPS, the maximum grafting density achievable is very low and such an interface fails by scission of the grafting chains so that the interface fracture toughness is also low. Large values of Gc are observed at intermediate chain lengths where both effective entanglements can be formed and a large Σ can be achieved. Under these conditions the interface fails initially due to the formation of crazes and the subsequent break down of one of these crazes at the interface. The transition areal chain density from chain scission to crazing, Σc,is independent of N.

Type
Research Article
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

REFERENCES

[1[ Washiyama, J., Kramer, E. J., Hui, C. Y., Macromolecules. 1993, 26, 2928.Google Scholar
[2] Dai, K.H; Kramer, E. J.; Fréchet, J. M. J.; Wilson, P. G.; Long, T. E.; Macromolecules, 1994, 27, 5187 Google Scholar
[3] Sha, Y., Hui, C.Y., Kramer, E.J., Hahn, S. and Berglund, C., Macromolecules. 1996, 29, 4728 Google Scholar
[4] Creton, C; Kramer, E. J.; Hui, C.Y.; Brown, H. R., Macromolecules. 1992, 25, 3075 Google Scholar
[5] Norton, L. J., Smigolova, V., Pralle, M. U., Hubenko, A., Dai, K. H., Kramer, E.J., Hahn, S., Berglund, C. and DeKoven, B., Macromolecules. 1995, 28, 1999.Google Scholar
[6] Kramer, E. J., Israel J.Chem. 1995, 35, 49 Google Scholar
[7] Onogi, S.; Masuda, T.; Kitagawa, K., Macromolecules 1970, 3, 109.Google Scholar