AB-polymer networks based on oligo(ɛ-caprolactone) segments showing shape-memory properties
Author(s) -
Andreas Lendlein,
Annette M. Schmidt,
Róbert Langer
Publication year - 2001
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.98.3.842
Subject(s) - comonomer , materials science , crystallinity , shape memory polymer , polymer , acrylate , shape memory alloy , composite material , ultimate tensile strength , glass transition , modulus , thermal stability , polymer chemistry , chemical engineering , polymerization , monomer , engineering
Although shape-memory metal alloys have wide use in medicine and other areas, improved properties, particularly easy shaping, high shape stability, and adjustable transition temperature, are realizable only by polymer systems. In this paper, a polymer system of shape-memory polymer networks based on oligo(ɛ-caprolactone) dimethacrylate as crosslinker andn -butyl acrylate as comonomer was introduced. The influence of two structural parameters, the molecular weight of oligo(ɛ-caprolactone) dimethacrylate and the weight content ofn -butyl acrylate, on macroscopic properties of polymer networks such as thermal and mechanical properties has been investigated. Tensile tests above and below melting temperature showed a decrease in the elastic modulus with increasing comonomer weight content. The crystallization behavior of the new materials has been investigated, and key parameters for the programming procedure of the temporary shape have been evaluated. Shape-memory properties have been quantified by thermocyclic experiments. All samples reached uniform deformation properties with recovery rates above 99% after 3 cycles. Whereas strain recovery increased with increasingn -butyl acrylate content, strain fixity decreased, reflecting the decreasing degree of crystallinity of the material.
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