Abstract

The JKR technique was used to determine the source and nature of the adhesion hysteresis present in modified poly(dimethylsiloxane) (PDMS) networks. As controlled excess amounts of the tetrafunctional crosslinker were added to the networks, the adhesion hysteresis increased. It was found that by poisoning the catalyst with a thiol the hysteresis could be significantly lowered, and completely removed in some cases. We believe that the adhesion hysteresis in this system stems from a complexation between the excess crosslinker and the catalyst. We found that the work of adhesion in this case is a function of the unloading rate. The unloading rate dependence of this chemical adhesion hysteresis was attributed to the rate of bond dissociation.

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