High-temperature polymer polyamide

Polyamide imide. see High-temperature polymers Polyamides... 

Diamantane-based polymers are synthesized to take advantage of their stiffness, chemical and thermal stability, high glass transition temperature, improved solubility in organic solvents, and retention of their physical properties at high temperatures. All these special properties result from their diamantane-based molecular structure [90]. Polyamides are high-temperature polymers with a broad range of applications in different scientific and industrial fields. However, their process is very difficult because of poor solubility and lack of adequate thermal stability retention [90]. Incorporation of 1,6- or... 

Some of the aromatic polyamides are thermally stable resins (cf. Section 5.1.5), the others can be transformed into high-temperature polymers by structural modifications. 

Studies of uniaxial extension on noncrystallizable elastomer, poly(phenyl methyl siloxane) showed results which are consistent and comparable with those obtained for PDMS, suggesting that the crystallization is not important for this type of reinforcement [20]. Other examples for reinforcement effects achieved with the addition of silica fillers include polyisobutylene [24], poly(ethyl acrylate) [3], poly (tetra methylene oxide) [29,30], and some high-temperature polymers such as aromatic polyamides [14,33,34], polyi-mides [15,38,39], polybenzoxazoles [16,17], and polyben-zobisthiazoles [16,17]. Results indicated that the modulus increases with increase in silica content while the tensile... 

Arnold C (1979) Stability of high-temperature polymers. J Polym Sci Macromol Rev 14 265-378 Beyler CL, Hirschler MM (1995) Thermal decomposition of polymers. In DiNenno PJ (ed) The SFPE handbook of fire protection engineering (Chaps. 1-7), 2nd edn. NFPA, Quincy, MA, pp 110-131 Bhuiyan AL (1984) Some aspects of the thermal stability action of the structure in aliphatic polyamides and polyacrylamides. Polymer 25 1699-1710... 

Bakelite was a thermoset that is, it did not flow after the synthesis was complete (20). The first synthetic thermoplastics, materials that could flow on heating, were poly(vinyl chloride), poly(styrene-5t t-butadiene), polystyrene, and polyamide 66 see Table 1.8 (20). Other breakthrough polymers have included the very high modulus aromatic polyamides, known as Kevlar (see Section 7.4), and a host of high temperature polymers. 

This chapter has provided a general summary of fatigue concepts, measurement techniques or methods, data presentation, and theory. It was meant to be introductory only and additional details should be obtained from the literature cited in this chapter [24-26], Chapters Styrenic Plastics, Polyether Plastics, Polyester Plastics, Polyimide Plastics, Polyamide Plastics (Nylons), Polyolefins and Acrylics, Thermoplastic Elastomers, Fluoropolymers, High-Temperature Polymers contain hundreds of plots of fatigue-related data on hundreds of different plastics. 

The field of step-growth polymers encompasses many polymer structures and polymerization reaction types. This chapter attempts to cover topics in step-growth polymerization outside of the areas reviewed in the other introductory chapters in this book, i.e., poly(aryl ethers), dendritic polymers, high-temperature polymers and transition-metal catalyzed polymerizations. Polyamides, polyesters, polycarbonates, poly(phenylene sulfides) and other important polymer systems are addressed. The chapter is not a comprehensive review but rather an overview of some of the more interesting recent research results reported for these step-growth polymers, including new polymerization chemistries and mechanistic studies. 

Wood fibers are often used to reinforce polyolefins but not high temperature polymers like polyamide 6 and 66. These polyamides melt above 200 °C, which is often considered the maximum processing temperature for wood fibers. A variety of techniques for compoimding and molding wood fiber/polyamide composites will be presented. These techniques are evaluated by examining fiber dispersion, fiber attrition and composite mechanical properties. 

Polyimides for use ia molded products and high temperature films can be produced by the reaction of pyromelHtic dianhydride [89-32-7] and 4,4 -diaminodiphenyl ether [13174-32-8] ia DMAC to form a polyamide that can be converted iato a polyimide (13). DMAC can also be used as a spinning solvent for polyimides. AdditionaUy, polymers containing over 50% vinyHdene chloride are soluble up to 20% at elevated temperatures ia DMAC. Such solutions are useful ia preparing fibers (14). 

Carboxyhc acids react with aryl isocyanates, at elevated temperatures to yield anhydrides. The anhydrides subsequently evolve carbon dioxide to yield amines at elevated temperatures (70—72). The aromatic amines are further converted into amides by reaction with excess anhydride. Ortho diacids, such as phthahc acid [88-99-3J, react with aryl isocyanates to yield the corresponding A/-aryl phthalimides (73). Reactions with carboxyhc acids are irreversible and commercially used to prepare polyamides and polyimides, two classes of high performance polymers for high temperature appHcations where chemical resistance is important. Base catalysis is recommended to reduce the formation of substituted urea by-products (74). 

Acid Chloride Reaction. In situations where the reactants are sensitive to high temperature or the polymer degrades before the melt poiat is reached, the acid chloride route is often used to produce the polyamide (47). The basic reaction ia the presence of a base, B , is as follows ... 

Polyamide or polyimide polymers are resistant to aliphatic, aromatic, and chlorinated or fluorinated hydrocarbons as well as to many acidic and basic systems but are degraded by high-temperature caustic exposures. 

Many of the polymers that are produced by the usual high-temperature reactions could be produced at lower temperatures by using the faster Schotten Baumann reactions of acid chlorides. Thus polyesters and polyamides could he produced by replacing the diacid or di-eser reactant by the corresponding diacyl chloride... 

Polycarbonate is blended with a number of polymers including PET, PBT, acrylonitrile-butadiene-styrene terpolymer (ABS) rubber, and styrene-maleic anhydride (SMA) copolymer. The blends have lower costs compared to polycarbonate and, in addition, show some property improvement. PET and PBT impart better chemical resistance and processability, ABS imparts improved processability, and SMA imparts better retention of properties on aging at high temperature. Poly(phenylene oxide) blended with high-impact polystyrene (HIPS) (polybutadiene-gra/f-polystyrene) has improved toughness and processability. The impact strength of polyamides is improved by blending with an ethylene copolymer or ABS rubber. 

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