EFFECTS OF SUBSTRATE MODIFICATION ON THE INTERFACIAL ADHESION OF ACRYLIC ELASTOMERS

Authors
Citation
D. Ahn et Kr. Shull, EFFECTS OF SUBSTRATE MODIFICATION ON THE INTERFACIAL ADHESION OF ACRYLIC ELASTOMERS, Langmuir, 14(13), 1998, pp. 3646-3654
Citations number
45
Categorie Soggetti
Chemistry Physical
Journal title
ISSN journal
07437463
Volume
14
Issue
13
Year of publication
1998
Pages
3646 - 3654
Database
ISI
SICI code
0743-7463(1998)14:13<3646:EOSMOT>2.0.ZU;2-P
Abstract
Axisymmetric adhesion tests are used to probe the adhesion between a c arboxylated, poly(n-butyl acrylate) (PNBA) elastomer and a variety of substrates. The elastomer is in the form of a hemispherical cap, which is pressed against a flat substrate to give a circular contact area. A standard fracture mechanics approach is used to relate the applied l oad and the radius of the contact area to the energy release rate, g w hich can be viewed as an adhesion energy. For a given substrate, g is a function of the crack velocity, v, defined as the time derivative of the contact radius. The contact pressure does not appear to play a ro le in the development of the adhesive forces, and the specific relatio nship between g and v depends on the substrate. In all cases this rela tionship can be adequately described by the empirical expression, g(v) = g(o)(l + (v/v)(0.6)). Values of g(o) are within a factor of about 2 of the expected thermodynamic work of adhesion, but values of v var y from 5.5 to 215 nm/s, depending on the detailed nature of the substr ate. Decreases in the adhesion energy, as quantified by a decrease in g(o) and/or an increase in v are determined primarily by the segmenta l mobility of the substrate molecules. Comparison of results for free and grafted PNBA chains indicates that translational diffusion of mole cules at the substrate is not required in order to substantially reduc e the adhesion energy.