Polyesters aromatic MCLCP

Low-molecular-weight liquid-crystalline compounds have been known for about 100 years. However, main chain liquid crystal polymers (MCLCPs) have attained prominence only in the last 15 years. In 1956 Flory predicted lyotropic behaviour and this theoretical prediction was well demonstrated in the synthetic polymer area with the discovery by Kwolek of the aramids, e.g. poly(/ -phenyleneterephthamide). This led to interest in thermotropic main chain LCPs and, although aromatic polyesters which are thermotropic were described during this period in patents issued to and Carborundum Co., their liquid-crystalline... [Pg.407]

Completely rigid rod-like molecules such as poly(4-oxybenzoyl) or poly( p-phenylene terephthalate) tend to be highly crystalline and intractable, with melting points above the decomposition temperature of the polymers (>450°C). The problem of thermotropic MCLCP design is to disrupt the regularity of the intractable para-linked aromatic polymers to the point at which mesomorphic behaviour is manifested below the decomposition temperature and the materials can be processed in fluid yet ordered states. The disruption must not, however, be taken to the stage where conventional isotropic fluid behaviour is preferred. These requirements that the polymer must retain some rod-like nature but at the same time be melt-processable below 400-450°C have limited thermotropic MCLCPs mainly to polymers based on the linear ester or ester/amide bonds. With polyester/ polyesteramides, disruption is normally achieved by the th ee copolymerization techniques outlined in Fig. 8.1, i.e. frustrated chain packing, flexible spacers and non-linear links. [Pg.408]

Fig. 8.13. DMA of a MCLCP containing kinks compared to an isotropic aromatic polyester. (-----) normalised DMA stiffness HBA.36 IA.32 HQ.32 (— —)...

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