Cross-linked elastomers containing reversibly binding side groups are capable of storing elastic energy on multiple time-scales, giving rise to shape-memory and self-healing properties.  [Li et al, Macromolecules, 44 #13, 5336-5343 (2011)]

Elastomers /Rubber
Materials

Shape Memory Materials

Recent US Patents

9/21/2010
7,799,243
Shape memory main-chain smectic-C elastomers

Mather; Rousseau and Qin of the University of Connecticut have developed and shape memory elastomer by hydrosilylation of a reaction mixture including a liquid crystalline diene, a crosslinking agent, and a bis(silyl hydride) compound.

Recent Journal Articles

Dynamic Mechanical Behavior of Photo-Cross-linked Shape-Memory Elastomers
(5336–5343)
Macromolecules 44 #13 (2011)
Li et al of the University of Rochester, New York, incorporated photo-cross-linkable benzophenone side groups were incorporated into linear macromers containing reversible (2-ureido-4-pyrimidinone, UPy) side groups.  This method enables melt-processing of shape-memory elastomers into complex permanent shapes, and samples can be prepared with much higher UPy-content. UV–vis spectroscopy was applied to study the efficacy of the cross-linking process.  Resulting elastomer networks with variable densities of covalent cross-links and reversibly associating side groups were systematically prepared and studied.  Dynamic mechanical analysis revealed the presence of two storage modulus plateaus: a high-temperature plateau attributed to covalent cross-links, and a lower temperature plateau attributed to both reversible and covalent cross-links.  Results also show that dynamic cross-links behave nearly as effectively as permanent cross-links below the UPy hydrogen bond transition and that the presence of a covalent network supports cooperative binding of UPy side groups.  (RDC 7/6/2011)