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Fabrication of Crosslinked Block Copolymer Nanoparticles Using Cold Vulcanization

Published online by Cambridge University Press:  15 March 2011

Sungwon Ma
Affiliation:
School of Polymer, Textile and Fiber Engineering, Georgia Institute of Technology, 801 Ferst Dr. NW, MRDC 1, Atlanta, GA 30332-0295, USA
Yonathan Thio
Affiliation:
School of Polymer, Textile and Fiber Engineering, Georgia Institute of Technology, 801 Ferst Dr. NW, MRDC 1, Atlanta, GA 30332-0295, USA
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Abstract

The aim of this study is to understand the crosslinked system of poly(styrene)-bpoly(isoprene) copolymer using cold vulcanization process as a facile method to produce anisometric nanoparticles. The morphologies of block copolymers could be controlled by the type of monomers, block junction, composition, and block size. A systematic methodology, utilizing cylindrical and lamellar morphologies of PS-b-PI copolymer, was used for producing fiber and sheet shaped nanoparticles. The cold vulcanization process was accomplished using sulfur monochloride (S2Cl2) as crosslinking agent. The microstructures and crosslinking density of crosslinked PS-b-PI copolymers were imaged and characterized. This study demonstrated the crosslinking of microphase separated block copolymer as a method to create particles with controlled size, shape, and physical properties.

Type
Research Article
Copyright
Copyright © Materials Research Society 2009

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References

REFERENCES

1. Glass, R., Moller, M. and Spatz, J. P., Nanotechnology 14 (10), 11531160 (2003).Google Scholar
2. Nishiyama, N. and Kataoka, K., in Polymer Therapeutics Ii: Polymers as Drugs, Conjugates and Gene Delivery Systems (2006), Vol. 193, pp. 67101.Google Scholar
3. Ruzette, A. V. and Leibler, L., Nature Materials 4 (1), 1931 (2005).Google Scholar
4. Thio, Y. S., Wu, J. X. and Bates, F. S., Macromolecules 39 (21), 71877189 (2006).Google Scholar
5. Bates, F. S., Science 251 (4996), 898905 (1991).Google Scholar
6. Helfand, E. and Wasserman, Z. R., Macromolecules 13 (4), 994998 (1980).Google Scholar
7. Leibler, L., Macromolecules 13 (6), 16021617 (1980).Google Scholar
8. Matsen, M. W. and Schick, M., Macromolecules 27 (23), 67616767 (1994).Google Scholar
9. Matsen, M. W. and Schick, M., Macromolecules 27 (24), 71577163 (1994).Google Scholar
10. Liu, G. J., Yan, X. H. and Duncan, S., Macromolecules 35 (26), 97889793 (2002).Google Scholar