Antioxidant Silicone Elastomers without Covalent Cross-Links.

Improved sustainability is associated with elastomers that readily breakdown in the environment at end of life and, as importantly, that can be reprocessed/reused long before end of life arises. We report the preparation of silicone elastomers that possess both thermoplasticity-reprocessability-and antioxidant activity. A combination of ionic and H-bonding links natural phenolic antioxidants, including catechol, pyrogallol, tannic acid, and others, to telechelic aminoalkylsilicones. The mechanical properties of the elastomers, including their processability, are intimately linked to the ratio of [ArOH]/[H2NR] that was found to be optimal when the ratio exceeded 1:1.

Compatibilization of porphyrins for use as high permittivity fillers in low voltage actuating silicone dielectric elastomers.

Polysiloxanes represent, because of their unusual properties, a material with great potential for use in dielectric elastomers (DEs), a promising class of electroactive polymers. Currently, their application as actuators is limited by the need for high driving voltages, as a result of the low relative permittivity possessed by polysiloxanes (∼2-3). Reducing these voltages can be achieved to some degree by using high permittivity additives to improve the permittivity of the polysiloxane. However, modifying such additives so that they are compatible with, and can be dispersed within, polysiloxane elastomers remains challenging. For reliable actuation, full miscibility is key. In this work the porphyrin 5,10,15,20-(tetra-3-methoxyphenyl)porphyrin (TPMP) was investigated as a high permittivity additive. Its behaviour was compared to the analogue that was derivatized with bis(trimethylsiloxy)methylsilane groups using the Piers-Rubinsztajn reaction to improve compatability with silicone formulations. The derivatized porphyrin was dispersed in elastomers and their dielectric and mechanical properties were evaluated. It was discovered that only low levels of incorporation (1-10%) of the siliconized TPMP - much lower than the parent TPMP - were needed to elicit improvements in the permittivity and electromechanical actuation of the elastomers; actuation strains of up to 43% could be achieved using this method.