%0 journal article
%@ 1042-7147
%A Farhan, M.,Chaganti, S.R.,Noechel, U.,Kratz, K.,Lendlein, A.

%D 2015
%J Polymers for Advanced Technologies
%N 12
%P 1421-1427 
%R doi:10.1002/pat.3702
%T Reversible shape-memory properties of surface functionalizable, crystallizable crosslinked terpolymers
%U https://doi.org/10.1002/pat.3702
12 
%X There is a high demand for polymer actuators comprising reactive groups at their surface in biotechnological or bioanalytical devices especially in microfluidics. In this work, we explored whether a thermoplastic poly[ethylene-co-(ethyl acylate)-co-(maleic anhydride)] (PEEAMA) terpolymer can be converted to a multifunctional shape-memory actuator by introducing covalent netpoints. In crosslinked PEEAMA (cPEEAMA) crystalline polyethylene (PE) domains with melting temperatures below 70°C should serve as actuation domains, responsible for the reversible shape change during cyclic heating and cooling, while higher melting PE crystals act as skeleton forming domains; finally maleic anhydride (MAH) groups enable surface modification of the polymeric substrate. cPEEAMAs with a fixed composition and various crosslink densities were prepared by thermally crosslinking of PEEAMA using different dicumyl peroxide (DCP) concentrations in the starting reaction mixture. A broad melting transition in the range of 50 to 90°C with a melting temperature interval of ∆Tm = 40°C, related to the crystalline PE domains, was observed for all polymer networks in differential scanning calorimetric experiments. Cyclic, thermomechanical uniaxial tensile tests revealed high reversible strains up to 17 ± 2%. A reversible change in long period during repetitive heating and cooling was observed in in situ small angle X-ray scattering experiments. Finally, a successful functionalization of the MAH groups at the cPEEAMA surface by reaction with ethylene diamine was confirmed by infrared spectroscopy analysis. The presented amino functionalized cPEEAMA substrates could be a candidate material for the preparation of adaptive microfluidic devices.