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Doping of Polyaniline by Corona Discharge

Published online by Cambridge University Press:  10 February 2011

Aldo E. Job
Affiliation:
Instituto de Física de São Carlos, Universidade de São Paulo, C.P. 369, São Carlos, 13560–970, SP, Brazil – giacometti@ifqsc.sc.usp.br
JosÉ A. Giacomett
Affiliation:
Instituto de Física de São Carlos, Universidade de São Paulo, C.P. 369, São Carlos, 13560–970, SP, Brazil – giacometti@ifqsc.sc.usp.br
Luiz H. C. Mattoso
Affiliation:
Centro Nacional de pesquisa e Desenvolvimento de Instrumentação Agropecuária CNPDIA/EMBRAPA, C.P. 741, São Carlos, 13560–970, SP, Brazil
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Abstract

It is well known that conductive polyaniline (PANI) films are usually doped by immersing dedoped PANI films in HCI solution. This paper shows that a corona discharge can be successfully employed to dope thin films of polyaniline coated on poly (ethylene terephthalate) films. Similarly to the conventional doping with aqueous HCl the process is accompanied by a color change from blue to green and the conductivity can be tuned in the range from 10−10 up to 0.3 Scm−1. Such new doping method presents several advantages over the conventional one namely, dry process, use of no chemicals, rapidity and no dopant migration. Measurements also showed that the conductivity persists for a long time as observed for films prepared in chemical solution doping. It is believed that this novel technique could be employed in a continuous doping process aiming to produce films with large area for anti electrostatic packing applications.

Type
Research Article
Copyright
Copyright © Materials Research Society 1998

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References

1. Huang, W.S., Humphrey, B.D., and Macdiarmid, A.G., J. Chem. Soc. Faraday Trans. 1, 82, 2385, (1986).Google Scholar
2. Roth, S. and Grauper, W., Synth. Met. 55–57, 3623(1993).Google Scholar
3. Huang, W. S., Angelopoulos, M., White, J. R., and Park, J. M., Mol. Cryst. Liq. Cryst., 189, 227(1990).Google Scholar
4. Angelopoulos, M., Shaw, J.M., Huang, W. S., and Kaplan, R. D., Mol. Cryst. Liq. Cryst., 189, 221(1990).Google Scholar
5. Malmonge, J.A. and Mattoso, L.H.C., Synth. Met. 84, 779(1997).Google Scholar
6. Wolszczak, M., Kroh, J., and Abdel-Hamid, M. M, Radiat. Phys. Chem., 45, 71(1995).Google Scholar
7. Giacometti, J. A. and Oliveira, O. N. Jr., IEEE Trans. Elec. Insul. 27, 924(1992).Google Scholar
8. Schaffert, R. M., “Electrophotographic -Part II”, Focal, 1975.Google Scholar
9. Hendricks, C.D., In “Electrostatics and its applications”, Edited by Moore, A.D., Wiley, Chapter 4, (1973), 5785 Google Scholar
10. Dias, C. J., Mendes, J. N. Marat, and Giacometti, J. A., J. Phys. D: Appl. Phys. 22, 663(1989).Google Scholar
11. Novak, I. and. Florian, , J. Mat. Sci. Lett., 14, 1021(1995).Google Scholar
12. Mattoso, L. H. C., Job, A. E. and Giacometti, J. A., Pending Patent INPI — Brazil (1997).Google Scholar
13. Mattoso, L. H. C., MacDiarmid, A. G., and Epstein, A. J., Synth. Met., 68, 1(1994).Google Scholar
14. Goldman, A. and Amoroux, J., in “Electrical Breakdown and Discharge in Gases, Macroscopic Processes and Discharges”, edited by Kunhardt, E. E. and Luessen, L. H., Plenum, New York, 1983.Google Scholar
15. In preparation.Google Scholar