Hostname: page-component-586b7cd67f-tf8b9 Total loading time: 0 Render date: 2024-11-29T01:58:18.150Z Has data issue: false hasContentIssue false

Electrical properties of polyethylene highly filled with carbon

Published online by Cambridge University Press:  31 January 2011

F. A. Modine
Affiliation:
Solid State Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831–6030
A. R. Duggal
Affiliation:
General Electric Company, Corporate Research and Development, Schenectady, New York 12301
D. N. Robinson
Affiliation:
Development Division, Oak Ridge Y-12 Plant, Oak Ridge, Tennessee 37831–8095
E. L. Churnetski
Affiliation:
Development Division, Oak Ridge Y-12 Plant, Oak Ridge, Tennessee 37831–8095
M. Bartkowiak
Affiliation:
Solid State Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831–6030
G. D. Mahan
Affiliation:
Solid State Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831–6032 and Department of Physics, University of Tennessee, Knoxville, Tennessee 37996
L. M. Levinson
Affiliation:
General Electric Company, Corporate Research and Development, Schenectady, New York 12301
Get access

Abstract

Carbon-filled polyethylene composites were fabricated and tested to establish the practical lower limit of their electrical resistivity at room temperature and to investigate the trade-offs between low resistivity and the magnitude of the resistance anomaly (i.e., a large positive temperature coefficient of resistivity) that appears when such composites are heated through the polyethylene crystalline melting transition. Carbon blacks with large particle size and low surface area provided low-resistivity composites having large resistance anomalies. The largest resistance anomalies were found in composites that were well mixed, but the room-temperature resistivity also increased in composites that were cycled repetitively through the crystalline-melting transition. A mixture of carbon blacks of two different sizes provided a lower resistance than was found in a material with the same fill of only the coarser black. By controlling the composition and the processing, composites were made with room-temperature resistivities lower than 0.2 ohm cm and resistance changes of at least 2 orders of magnitude. A resistance change of as much as 5 orders of magnitude was obtained for composites with room-temperature resistivities of only 1 ohm cm.

Type
Articles
Copyright
Copyright © Materials Research Society 1996

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.Carbon Black Polymer Composites, edited by E. K. Sichel (Marcel Dekker, New York, 1982).Google Scholar
2.Bueche, F., J. Appl. Phys. 44, 532 (1973).CrossRefGoogle Scholar
3.Doljack, F. A., IEEE Trans. Comp., Hybrids, Manuf. Tech. Chmt. 4, 372 (1981).CrossRefGoogle Scholar
4.Narkus, M., Ram, A., and Flashner, F., Polym. Eng. Sci. 18, 649 (1978).CrossRefGoogle Scholar
5.Benguigui, L., Yacubowicz, J., and Narkus, M., J. Polym. Sci. 25, 127 (1987).CrossRefGoogle Scholar
6.Ohe, K. and Naito, Y., Jpn. J. Appl. Phys. 10, 99 (1971).CrossRefGoogle Scholar
7.Sherman, R. D., Middleman, L. M., and Jacobs, S. M., Polym. Eng. Sci. 23, 36 (1983).CrossRefGoogle Scholar
8.Sarychev, A. K. and Brouers, F., Phys. Rev. Lett. 73, 2895 (1994).CrossRefGoogle Scholar
9.Meyer, J., Polym. Eng. Sci. 13, 462 (1973).CrossRefGoogle Scholar
10.Rajagopal, C. and Satyam, M., J. Appl. Phys. 49, 5536 (1978).CrossRefGoogle Scholar
11.Narkus, M. and Vaxman, A., J. Appl. Polym. Sci. 29, 1639 (1984).CrossRefGoogle Scholar
12.Ruschau, G. R., Yoshikawa, S., and Newnham, R. E., Proc. 42nd IEEE Electronic Components and Technol. Conf. p. 481, May 18–20, 1992.Google Scholar
13.Narkus, M., Ram, A., and Stein, Z., Polym. Eng. Sci. 21, 1049 (1981).CrossRefGoogle Scholar
14.Tang, H., Piao, J., Chen, X., Luo, Y., and Li, S., J. Appl. Polym. Sci. 48, 1795 (1993).CrossRefGoogle Scholar
15.Meyer, J., Polym. Eng. Sci. 14, 706 (1974).CrossRefGoogle Scholar
16.Brodeur, S. A., Huebner, W., Runt, J. P., and Newnham, R. E., J. Mater. Res. 6, 175 (1991).CrossRefGoogle Scholar