Please use this identifier to cite or link to this item:;2-Y
Title: Surface study of ladderlike polyepoxysiloxanes
Authors: Chen, W.-Y.
Lin, Y.
Pramoda, K.P.
Ma, K.X.
Chung, T.S. 
Issue Date: 1-Jan-2000
Citation: Chen, W.-Y.,Lin, Y.,Pramoda, K.P.,Ma, K.X.,Chung, T.S. (2000-01-01). Surface study of ladderlike polyepoxysiloxanes. Journal of Polymer Science, Part B: Polymer Physics 38 (1) : 138-147. ScholarBank@NUS Repository.;2-Y
Abstract: By using the two-liquid geometric method and the three-liquid acid-base method, we are the first to determine the surface tensions of ladderlike polyepoxysiloxanes by the measurement of contact angles on thin films. Three kinds of ladderlike polymers have been synthesized: A-C (which has the alkyl group and the epoxy group graft to the ladderlike polysilsesquioxane chain), A-C-P (which has the alkyl group, phenyl group, and epoxy group graft to the ladderlike chain), and A-P (which has the phenyl group and epoxy group in the ladderlike side chain). The results showed that when different liquids and different theories are chosen to determine the surface energies, there are some minor differences in the values but a similar trend is still exhibited. The surface energies of these three polymers are in the following order of γSA-CA-P, suggesting Si atoms were more likely to migrate to the polymer surface and the bulky effect of the phenyl groups could also interfere with the migration of the Si atoms. As a result, Si and O ratio at the interface determines the order of apparent surface energy for these three polymers. Experimental data also reflect that there are differences between the ladderlike polyepoxysiloxanes and the commercially available linear polysiloxanes.
Source Title: Journal of Polymer Science, Part B: Polymer Physics
ISSN: 08876266
DOI: 10.1002/(SICI)1099-0488(20000101)38:13.0.CO;2-Y
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
There are no files associated with this item.

Page view(s)

checked on Jul 6, 2018

Google ScholarTM



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.