Abstract

The shape-memory response (SMR) of “click” thiol-epoxy polymers produced using latent catalysts, with different network structure and thermo-mechanical properties, was tested on unconstrained shape-recovery processes under isothermal conditions. Experiments at several programming temperatures ( $T_{\mathrm{prog}}$ ) and isothermal-recovery temperatures ( $T_{\mathrm{iso}}$ ) were carried out, and the shape-memory stability was analyzed through various consecutive shape-memory cycles. The temperature profile during the isothermal-recovery experiments was monitored, and it showed that the shape-recovery process takes place while the sample is becoming thermally stable and before stable isothermal temperature conditions are eventually reached. The shape-recovery process takes place in two different stages regardless of $T_{\mathrm{iso}}$ : a slow initial stage until the process is triggered at a temperature strongly related with the beginning of network relaxation, followed by the typical exponential decay of the relaxation processes until completion at a temperature below or very close to $T_{\mathrm{g}}$ . The shape-recovery process is slower in materials with more densely crosslinked and hindered network structures. The shape-recovery time ( $t_{\mathrm{sr}}$ ) is significantly reduced when the isothermal-recovery temperature $T_{\mathrm{iso}}$ increases from below to above $T_{\mathrm{g}}$ because the network relaxation dynamics accelerates. However, the temperature range from the beginning to the end of the recovery process is hardly affected by $T_{\mathrm{iso}}$ ; at higher $T_{\mathrm{iso}}$ it is only slightly shifted to higher temperatures. These results suggest that the shape-recovery process can be controlled by changing the network structure and working at $T_{\mathrm{iso}} < T_{\mathrm{g}}$ to maximize the effect of the structure and/or by increasing $T_{\mathrm{iso}}$ to minimize the effect but increasing the shape-recovery rate.

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