Hostname: page-component-586b7cd67f-rdxmf Total loading time: 0 Render date: 2024-11-26T10:08:26.967Z Has data issue: false hasContentIssue false

Retarded Cross-linking in ZnO-low-density Polyethylene Nanocomposites

Published online by Cambridge University Press:  31 January 2011

J.I. Hong
Affiliation:
Materials Science and Engineering Department and Rensselaer Nanotechnology Center, Rensselaer Polytechnic Institute, Troy, New York 12180
K. S. Cho
Affiliation:
Materials Science and Engineering Department and Rensselaer Nanotechnology Center, Rensselaer Polytechnic Institute, Troy, New York 12180
C. I. Chung
Affiliation:
Materials Science and Engineering Department and Rensselaer Nanotechnology Center, Rensselaer Polytechnic Institute, Troy, New York 12180
L. S. Schadler
Affiliation:
Materials Science and Engineering Department and Rensselaer Nanotechnology Center, Rensselaer Polytechnic Institute, Troy, New York 12180
R. W. Siegel
Affiliation:
Materials Science and Engineering Department and Rensselaer Nanotechnology Center, Rensselaer Polytechnic Institute, Troy, New York 12180
Get access

Extract

ZnO nanoparticles were mixed with branched low-density polyethylene and were found to increase the resistance of the polymer to thermal degradation without changing other thermal properties. Submicron-size ZnO particles were mixed with low-density polyethylene for comparison, and it was found that the increased thermal stability of the nanocomposite was due to the surface properties of nanoparticles smaller than approximately 100 nm in diameter.

Type
Rapid Communications
Copyright
Copyright © Materials Research Society 2002

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.Gleiter, H., Prog. Mater. Sci. 33, 223 (1989).Google Scholar
2.Nanophase Materials: Synthesis, Properties, Applications edited by Hadjipanayis, G.C. and Siegel, R.W. (Kluwer, Dordrecht, The Netherlands, 1994).Google Scholar
3.Godovsky, D.Y., Adv. Polym. Sci. 119, 79 (1995).Google Scholar
4.Siegel, R.W., Nanostruct. Mater. 3, 1 (1993).Google Scholar
5.Godovsky, D.Y., Adv. Polym. Sci. 153, 163 (2000).Google Scholar
6.Siegel, R.W., Mater. Sci. Eng. A 168, 189 (1993).CrossRefGoogle Scholar
7.Vassiliou, J.K., Mehrotra, V., Russell, M.W., Giannelis, E.P., McMichael, R.D., Shull, R.D., and Ziolo, R.F., J. Appl. Phys. 73, 5109 (1993).CrossRefGoogle Scholar
8.Sumita, M., Tsukumo, Y., Miyasaka, K., and Ishikawa, K., J. Mater. Sci. 18, 1758 (1983).CrossRefGoogle Scholar
9.Cole, D.H., Shull, K.R., Baldo, P., and Rehn, L., Macromolecules 32, 771 (1999).Google Scholar
10.Gulgun, M.A., Kriven, W.M., Tan, L.S., and McHugh, A.J., J. Mater. Res. 10, 1746 (1995).Google Scholar
11.Tan, L.S., McHugh, A.J., Gulgun, M.A., and Kriven, W.M., J. Mater. Res. 11, 1739 (1996).Google Scholar
12.Wang, Y. and Herron, N., J. Phys. Chem. 95, 525 (1991); Phy. Rev. B 42, 7253 (1991).CrossRefGoogle Scholar