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polymers is their long-molec- polymers, on the other hand, control than production of necessary to obtain elas-
ular-chain structure. Liquid the mesogen are joined to the main-chain LCP [2]. tomeric properties starts im-
crystalline polymers (LCP) polymer backbone using a Liquid crystalline elas- mediatley before mechanical
combine these polymer prop- spacer. In this case, polymeri- tomers (LCE) are produced by stretching and so “freezes” the
erties with the anisotropy of sation of the backbone can weak crosslinking of LCP. ordered molecular arran-
liquid crystals. Special crys- take place before or after at- Owing to the low density of gement achieved by stretch-
talline molecular units (meso- taching the mesogens. Since the polymer chains, the re- ing.
gens) are responsible for the the backbone and mesogens sulting material has rubber- When the temperature is
crystalline behaviour. There can be created independently elastic properties (Table 1). increased in the immediate
are basically two ways in of each other, production of Siloxanes are a particularly in- environment of actuator ma-
which these mesogens can terial produced by this
be combined with polymer Properties Values method, the ordering of the
chains [1]: in the case of main Hardness Shore A 10–80 mesogens is lost [4]. The rea-
polymer chains, the mesogens Tensile strength MPa 0.2–0.6
son for this change of shape is
can be inserted directly into the transition of the material
the polymer chain to produce Actuator stress kPa 21–60 from the liquid crystalline to
liquid crystalline main-chain Uniaxial deformation (L0/L)*100 % 140–160 the isotropic phase by thermal
TNI °C 30–120 fluctuation (nematic-isotrop-
ic transition; Fig. 1). The re-
TG °C -10–24
Translated from Kunststoffe 10/2006, versibility of this change de-
pp. 30–34 Table 1. Some typical properties of liquid crystalline elastomers pends on the elasticity of the