Elastic behavior liquid crystals, nematic phase

Neither does the microbrownian motion of the amorphous mesh inhibit the liquid crystal phase, nor does the positional order of the molecules interfere with the elasticity. Hence, as a hybrid material that combines LC and rubber characteristics, LCEs have unique properties in which the molecular orientation of the liquid crystal is strongly correlated with the macroscopic shape (deformation) which is unparalleled to other materials. The most prominent example in the physical properties derived from this property is the huge thermal deformation. Figure 10.1 shows an example of the thermal deformation behavior of side-chain nematic elastomers (NE) [3]. When the molecules transform from the random orientation in the isotropic phase to the macroscopic planar orientation in the nematic phase, the rubber extends in the direction of the liquid crystal orientation and increases with decreasing temperature as a result of an increase in the degree of liquid crystal orientation. This thermal deformation behavior is reversible, and LCEs can be even considered as a shape-memory material. Figure 10.1 is from a report of the early research on thermal deformation of LCEs, and a strain of about 40 % was observed [3]. It is said that LCEs show the largest thermal effect of all materials, and it has been reported that the thermal deformation reaches about 400 % in a main-chain type NE [4]. 

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