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Aromatic Polyester with Flexible Links

As flexible substituents, linear and branched alkyl, alkoxy, or thioalkyl side chains of different lengths have been utilized to modify para-linked aromatic polyesters. The main difference to the systems discussed above is the limited thermal stability caused by the substitution with alkyl chains. Also, the mechanical poperties are substantially lowered with increasing... [Pg.16]

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]


See other pages where Aromatic Polyester with Flexible Links is mentioned: [Pg.369]    [Pg.109]    [Pg.102]    [Pg.39]    [Pg.126]    [Pg.430]    [Pg.398]    [Pg.79]    [Pg.43]    [Pg.208]    [Pg.451]    [Pg.1200]    [Pg.13]    [Pg.492]    [Pg.2075]    [Pg.421]    [Pg.653]   
See also in sourсe #XX -- [ Pg.198 , Pg.200 ]




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