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Proceedings Paper

Ion transfer in contact electrification
Author(s): Arthur F. Diaz; Debra Fenzel-Alexander; Daphne Wollmann; A. Eisenberg
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Paper Abstract

The contact charge on polymers is influenced by added organic salts, and the charge is higher when the additive is polymer-bound rather than molecular.'7 In our studies, the presence of an ionomer consisting of a polystyrene random copolymer with pendent N-methylpyridinium toluenesulfonate groups in the host resin produces a positive charge, and the charge is higher than with the molecular analog, 4-ethyl-N-methylpyridinium toluenesulfonate.68 These studies were made with powders, and the charge was activated by rolling the powder with larger sized particles. The charging is attributed to ion transfer, where the toluenesulfonate anion (OTs) transfers from one particle surface to the other, and the proposal is supported by the observation of OTs on the second surface by XPS. l'he different charge levels were attributed to the relative mobilities of the cation and the anion, where in the ionomers, the cation is 'anchored' to the polymer and only OTs is mobile. With the molecular salt, both ions can transfer, although in unequal amounts, thus producing a smaller net charge. We now report our results from the analyses of the charged powders with a Simpson charge spectrometer, which allow us to relate the charge distributions with the charge levels in these materials.

Paper Details

Date Published: 1 July 1990
PDF: 5 pages
Proc. SPIE 1253, Hard Copy and Printing Materials, Media, and Processes, (1 July 1990); doi: 10.1117/12.19838
Show Author Affiliations
Arthur F. Diaz, IBM/Almaden Research Ctr. (United States)
Debra Fenzel-Alexander, IBM/Almaden Research Ctr. (United States)
Daphne Wollmann, IBM/Almaden Research Ctr. (United States)
A. Eisenberg, McGill Univ. (Canada)


Published in SPIE Proceedings Vol. 1253:
Hard Copy and Printing Materials, Media, and Processes
Joseph Gaynor, Editor(s)

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