Aromatic polyamides stabilization methods

Some three decades ago, scientists from the Du Pont company developed polycondensation methods which allowed the preparation of high molecular weight wholly aromatic polyamides. The first commercially produced wholly aromatic polyamide fibre was poly(m-phenyleneisophthalamide) (Nomex, Du Pont, 1967) [la, c]. Some years later, development of the preparation and processing of poly(p-phenyleneterephthalamide) (PPTA) led to the commercialization of the para product Kevlar (Du Pont) in the early seventies [lb, c]. While Nomex shows excellent thermal stability and flame-retardance, and indeed is referred to as a heat and flame resistant aramid fibre, Kevlar fibre also has similar properties, but in addition it has exceptional tensile strength and modulus, and is referred to as an ultra-high strength, high modulus aramid fibre. 

There are some indications that the self-assembly method yields sufficiently stable structures. Kwak et al. (2001) used a self-assembly method for Ti02 nanoparticles with a size of 2 nm for aromatic polyamide reverse osmosis membranes, in view of flux enhancement they applied X-ray photoelectron spectroscopy to observe the stability of the attachment of the nanoparticles and concluded that the adsorbed particles were sufficiently tightly bound to the surface to withstand various washing procedures and even harsh reverse osmosis-operating conditions. 

The use of tetracarboxylic acid anhydride instead of the dicarboxylic acids used in the manufacture of polyamides yields polyimides. The general method of preparation of the original polyimides by the polymerization of pyromellitic dianhydride and aromatic diamine is shown in Figure 1.18a. A number of diamines have been investigated, and it has been found that certain aromatic amines, which include m-phenylendediamine, benzidine, and di-(4-aminophenyl)ether, give polymers with a high degree of oxidative and thermal stability. 

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