Effect of the type of plasma on the polydimethylsiloxane/collagen composites adhesive properties
Polydimethylsiloxane (PDMS) films were treated with either oxygen (O2), nitrogen (N2) or argon (Ar) plasma between 40W and 120W for 5–15min and their surface properties studied by contact angle measurements, infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and atomic force microscopy...
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Published in | International journal of adhesion and adhesives Vol. 77; pp. 85 - 95 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Kidlington
Elsevier Ltd
01.09.2017
Elsevier BV |
Subjects | |
Online Access | Get full text |
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Summary: | Polydimethylsiloxane (PDMS) films were treated with either oxygen (O2), nitrogen (N2) or argon (Ar) plasma between 40W and 120W for 5–15min and their surface properties studied by contact angle measurements, infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and atomic force microscopy (AFM). Lower contact angles and increases in surface roughness, assessed by SEM and AFM, were observed for all used gases when plasma power and time increased, with argon treatment being the one that showed the most significant change in roughness.
PDMS/collagen type I composites obtained after treating PDMS with oxygen at 80W for 13min or nitrogen and argon at 80W for 14min showed a peel strength of 0.1N/mm (oxygen plasma), 0.08 N/mm (nitrogen plasma) and 0.09 N/mm (argon plasma). In all cases, peel strength was higher than that measured for the untreated bilayer composite. An increase in adhesion strength, after oxygen and nitrogen plasma, was mostly attributed to chemical interaction between functional groups introduced on the PDMS surface and the functional groups on collagen as detected by FTIR. In contrast, the high peel strength observed on PDMS treated with argon plasma was attributed to its increased roughness which in turn increased mechanical interlocking. The properties of these composites render them suitable for adhesive free skin substitutes. |
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ISSN: | 0143-7496 1879-0127 |
DOI: | 10.1016/j.ijadhadh.2017.03.010 |