The University of Southampton
University of Southampton Institutional Repository

Charge separation associated with contact charging between polymers

Charge separation associated with contact charging between polymers
Charge separation associated with contact charging between polymers

Experimental investigations have been carried out on the polarity and magnitude of the charge transferred after multiple contacts between 1W different pairs of commercial polymers. Equilibrium contact angles between the 10 different polymer samples and a selection of pure organic liquids were determined. The surface energy value of a given polyner sample was obtained from a graphical plot of the cosine of the equilibrium contact angle versus the surface tension of the liquid and applying the Zisman relationship. The polymer samples were arranged in order of decreasing surface energy values. It was observed that the middle order neighbouring polymers were very close in surface energy values. A contact charging series was arranged such that a given polymer making multiple contacts with another polymer above it in the series charged negative. It charged positive after making multiple contacts with another polymer below it in the series. A few pairs did not obey this rule, including those whose members had been cut from the same polymer. Causes of the inconsistency were contributed to, inter alia, the relative humidity of the experimental conditions, the observed closeness in the surface energy values and a second order effect. An interesting relationship was observed between the arrangement of the polymer, surface energy values, and the contact charging series. This meant that the polarity of the charge transferred between 2 dissimilar commercial polymers after successive multiple contacts could be determined by a consideration of the surface energy values. The hi & pr surface energy polymer tended to charge positive with respect to the lower surface energy polymer. The magnitude of the charge transferred seemed not to depend on the position of a polymer in the series. It varied a great deal. It was also observed that provided experiments are performed with reasonable amount of care and following reasonable surface-cleaning, the hitherto widely believed need to perform experiments in vacuum was not essential. Attempts were made to correlate some of the authors' results with results published by manufacturers as the true nature of a polymer surface depends on the manufacturer's specification of colour, grade, finish, additives used, etc. it became evident that in situ measurements had to be done on all samples before generalisations can be made on the correlation.

University of Southampton
Magezi, Daudi Subi
Magezi, Daudi Subi

Magezi, Daudi Subi (1980) Charge separation associated with contact charging between polymers. University of Southampton, Doctoral Thesis.

Record type: Thesis (Doctoral)

Abstract

Experimental investigations have been carried out on the polarity and magnitude of the charge transferred after multiple contacts between 1W different pairs of commercial polymers. Equilibrium contact angles between the 10 different polymer samples and a selection of pure organic liquids were determined. The surface energy value of a given polyner sample was obtained from a graphical plot of the cosine of the equilibrium contact angle versus the surface tension of the liquid and applying the Zisman relationship. The polymer samples were arranged in order of decreasing surface energy values. It was observed that the middle order neighbouring polymers were very close in surface energy values. A contact charging series was arranged such that a given polymer making multiple contacts with another polymer above it in the series charged negative. It charged positive after making multiple contacts with another polymer below it in the series. A few pairs did not obey this rule, including those whose members had been cut from the same polymer. Causes of the inconsistency were contributed to, inter alia, the relative humidity of the experimental conditions, the observed closeness in the surface energy values and a second order effect. An interesting relationship was observed between the arrangement of the polymer, surface energy values, and the contact charging series. This meant that the polarity of the charge transferred between 2 dissimilar commercial polymers after successive multiple contacts could be determined by a consideration of the surface energy values. The hi & pr surface energy polymer tended to charge positive with respect to the lower surface energy polymer. The magnitude of the charge transferred seemed not to depend on the position of a polymer in the series. It varied a great deal. It was also observed that provided experiments are performed with reasonable amount of care and following reasonable surface-cleaning, the hitherto widely believed need to perform experiments in vacuum was not essential. Attempts were made to correlate some of the authors' results with results published by manufacturers as the true nature of a polymer surface depends on the manufacturer's specification of colour, grade, finish, additives used, etc. it became evident that in situ measurements had to be done on all samples before generalisations can be made on the correlation.

This record has no associated files available for download.

More information

Published date: 1980

Identifiers

Local EPrints ID: 459134
URI: http://eprints.soton.ac.uk/id/eprint/459134
PURE UUID: e92bc676-436f-4dd7-ae51-10d14f30f546

Catalogue record

Date deposited: 04 Jul 2022 17:05
Last modified: 04 Jul 2022 17:05

Export record

Contributors

Author: Daudi Subi Magezi

Download statistics

Downloads from ePrints over the past year. Other digital versions may also be available to download e.g. from the publisher's website.

View more statistics

Atom RSS 1.0 RSS 2.0

Contact ePrints Soton: eprints@soton.ac.uk

ePrints Soton supports OAI 2.0 with a base URL of http://eprints.soton.ac.uk/cgi/oai2

This repository has been built using EPrints software, developed at the University of Southampton, but available to everyone to use.

We use cookies to ensure that we give you the best experience on our website. If you continue without changing your settings, we will assume that you are happy to receive cookies on the University of Southampton website.

×