Liquid-Gas Phase Transition Actuator: Rejuvenation Procedure Extended and Open-Air Performance.

To achieve the actuation of silicone-based foamed composites, a liquid-gas phase transition of the liquid captured in its pores is employed. The uncertainty of key parameters for a single or sequential open-air performance of such soft actuators limits their application. To define the main characteristics of the composites, in this work, two functions of the liquid there were separated: the pore-forming agent (FPA) and working liquid (WL).

Synthesis of Vinyl-Containing Polydimethylsiloxane in An Active Medium.

This research deals with the synthesis of copoly(methylvinyl)(dimethyl)siloxanes by the copolycondensation of dimethyldiethoxy- and methylvinyldimethoxysilane in an active medium, followed by thermal condensation in a vacuum. We achieved a range of copolymers exhibiting finely tuned molecular weights spanning between 1500 and 20,000 with regulated functional methylvinylsiloxane units. Analysis of the microstructure showed that the copolymerization predominantly formed products demonstrating a random distribution of units (R~1).

A Concise Guide to Silicone-Based Spring-Roll Actuator Assembly.

A spring-roll actuator is a multilayer configuration of dielectric elastomer actuators that deforms in response to an electric field. To date, all spring-roll actuators are based on acrylate dielectric elastomers (DEs), and a few can reach deformations on a par with strains observed in natural muscles. Sensitivity to temperature and humidity, as well as the slow response times of acrylates, limit the commercialisation of these actuators.

Synthesis of 1,1,3,3,5,5-Hexamethyl-7,7-diorganocyclotetrasiloxanes and Its Copolymers.

This paper reports a method for the synthesis of 1,1,3,3,5,5-hexamethyl-7,7-diorganocyclotetrasiloxanes by the interaction of 1,5-disodiumoxyhexamethylsiloxane with dichlorodiorganosilanes such as methyl-, methylvinyl-, methylphenyl-, diphenyl- and diethyl dichlorosilanes. Depending on the reaction conditions, the preparative yield of the target cyclotetrasiloxanes is 55-75%. Along with mixed cyclotetrasiloxanes, the proposed method leads to the formation of polymers with regular alternation of diorganosylil and dimethylsylil units.