High-temperature polymer polycarbonate

The tetrazole (66) decomposes to yield nitrogen and a residue consisting of three main components aminodiphenyltriazole, 3,5-diphenyl-l,2,4-triazole and triphenyl-s-triazine (81MIH510, 69USP3442829). The inert nature of the decomposition products makes (66) suitable for use with high temperature polymers such as polycarbonate, polyester and Nylon 6. 

Liquid colors are compatible with a wide variety of polymers, including PVC, polyethylene vinyl acetate (EVA), nylons, PET, polycarbonate, alloys, high-temperature polymers, and the full range of polyolefins and styrenics. Many liquid colors are suitable to color food-contact polymers and comply with all government regulations worldwide for shipping, use, and disposal. Lead times for liquid color are typically less than those for pellet or other melted color concentrates, since the processing is quick and efficient. 

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. 

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. 

Kawai (1) and (2) (1969) found that polar polymer films such as PVDF, poly (vinyl fluoride), PVC, nylon 11, and polycarbonate exhibit a strong piezoelectricity when they are drawn and then polarized under a high cLc. field Ep at a high temperature Tp and cooled keeping the d.c. field. The piezoelectricity thus obtained depends on Ep, Tp, and poling period. An improved poling technique was reported by Edelman, Grisham, Roth, and Cohen (1970). 

Much attention has been paid to the synthesis of fluorine-containing condensation polymers because of their unique properties (43) and different classes of polymers including polyethers, polyesters, polycarbonates, polyamides, polyurethanes, polyimides, polybenzimidazoles, and epoxy prepolymers containing pendent or backbone-incorporated bis-trifluoromethyl groups have been developed. These polymers exhibit promise as film formers, gas separation membranes, seals, soluble polymers, coatings, adhesives, and in other high temperature applications (103,104). Such polymers show increased solubility, glass-transition temperature, flame resistance, thermal stability, oxidation and environmental stability, decreased color, crystallinity, dielectric constant, and water absorption. 

The mechanical properties of poly(methyl methacrylate), PMMA, have been studied for quite a long time and, in addition to its industrial interest, PMMA constitutes a kind of reference material. Indeed, among the amorphous linear polymers it represents an intermediate between the very brittle polystyrene and the tough bisphenol A polycarbonate considered in Sect. 4. Furthermore, as shown in [1] (Sect. 8.1), the molecular motions responsible for its large p transition are precisely identified, as well as the nature of the cooperativity that develops in the high temperature range of the p transition. 

Th-FFF can be applied to almost all kinds of synthetic polymers, like polystyrene, polyolefins, polybutadiene, poly(methyl methacrylate), polyisoprene, polysulfone, polycarbonate, nitrocelluloses and even block copolymers [114,194,220]. For some polymers like polyolefins, with a small thermal diffusion coefficient, high temperature Th-FFF has to be applied [221]. Similarly, hydrophilic polymers in water are rarely characterized by Th-FFF, due to the lack of a significant thermal diffusion (exceptions so far poly(ethylene oxide), poly(vi-nyl pyrrolidone) and poly(styrene sulfonate)) [222]. Thus Th-FFF has evolved as a technique for separating synthetic polymers in organic solvents [194]. More recently, both aqueous and non-aqueous particle suspensions, along with mixtures of polymers and particles, have been shown to be separable [215]. 

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