Shape Memory: An Efficient Method to Develop the Latent Photopatterned Morphology for Elastomer in Two/Three Dimension

Shape memory behavior was applied here as a new approach for developing the latent photopatterned morphologies in two/three dimension (2D/3D) on the modified poly­(styrene-<i>block</i>-butadiene-<i>block</i>-styrene) (SBS). By attaching anthracene groups onto the SBS chains, the elastomer frozen in the deformed state was photopatterned via the photodimerization of anthracene. Upon thermal treatment, shape memory process could effectively develop the latent photopatterning induced 2D–2D and 2D–3D shape transformation. Due to the reversible dimerization of anthracene, the photoinduced patterns and the shape conformation could be erased and redeveloped for multiple times

Dynamically Cross-linked Elastomer Hybrids with Light-Induced Rapid and Efficient Self-Healing Ability and Reprogrammable Shape Memory Behavior

Pristine carbon nanotubes (CNTs) were activated to exhibit Diels–Alder (DA) reactivity in a polymer matrix, which was modified with monomers containing furan groups. The DA-active polymer matrix was transferred into a dynamic reversible cross-linked inorganic–organic network via a Diels–Alder reaction with CNTs, where pristine CNTs were used as dienophile chemicals and furan-modified SBS acted as the macromolecular diene. In this system, the mechanical properties as well as resilience and solvent resistance were greatly improved even with the presence of only 1 wt % CNTs. Meanwhile, the hybrids retained recyclability and exhibited some smart behaviors, including self-healing and reprogrammable shape memory properties. Furthermore, due to the photothermal effect of CNTs, a retro-Diels–Alder (rDA) reaction was activated under laser irradiation, and healing of a crack on the hybrid surface was demonstrated in approximately 10 s with almost complete recovery of the mechanical properties. Such fast and efficient self-healing performance provides a new concept in designing self-healing nanocomposites with tunable structures and mechanical properties. Furthermore, the DA and rDA reactions could be combined to reprogram the shape memory behavior under laser irradiation or thermal treatment, wherein the temporary shape of the sample could be transferred to a permanent shape via the rDA reaction at high temperature

Unzipped Multiwalled Carbon Nanotube Oxide/Multiwalled Carbon Nanotube Hybrids for Polymer Reinforcement

Multiwalled carbon nanotubes (MWNTs) have been widely used as nanofillers for polymer reinforcement. However, it has been restricted by the limited available interface area of MWNTs in the polymer matrices. Oxidation unzipping of MWNTs is an effective way to solve this problem. The unzipped multiwalled carbon nanotube oxides (UMCNOs) exhibit excellent enhancement effect with low weight fractions, but agglomeration of UMCNOs at a relatively higher loading still hampered the mechanical reinforcement of polymer composites. In this paper, we interestingly found that the dispersion of UMCNOs in polymer matrices can be significantly improved with the combination of pristine MWNTs. The hybrids of MWNTs and UMCNOs (U/Ms) can be easily obtained by adding the pristine MWNTs into the UMCNOs aqueous dispersion, followed by sonication. With a π-stacking interaction, the UMCNOs were attached onto the outwalls of MWNTs. The morphologies and structure of the U/Ms were characterized by several measurements. The mechanical testing of the resultant poly­(vinyl alcohol) (PVA)-based composites demonstrated that the U/Ms can be used as ideal reinforcing fillers. Compared to PVA, the yield strength and Young’s modulus of U/M–PVA composites with a loading of 0.7 wt % of the U/Ms approached ∼145.8 MPa and 6.9 GPa, respectively, which are increases of ∼107.4% and ∼122.5%, respectively. The results of tensile tests demonstrated that the reinforcement effect of U/Ms is superior to the individual UMCNOs and MWNTs, because of the synergistic interaction of UMCNOs and MWNTs