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Poly high-performance materials

Table 6 shows the sales estimates for principal film and sheet products for the year 1990 (14). Low density polyethylene films dominate the market in volume, followed by polystyrene and the vinyls. High density polyethylene, poly(ethylene terephthalate), and polypropylene are close in market share and complete the primary products. A number of specialty resins are used to produce 25,000—100,000 t of film or sheet, and then there are a large number of high priced, high performance materials that serve niche markets. The original clear film product, ceUophane, has faUen to about 25,000 t in the United States, with only one domestic producer. Table 7 Hsts some of the principal film and sheet material manufacturers in the United States. Table 6 shows the sales estimates for principal film and sheet products for the year 1990 (14). Low density polyethylene films dominate the market in volume, followed by polystyrene and the vinyls. High density polyethylene, poly(ethylene terephthalate), and polypropylene are close in market share and complete the primary products. A number of specialty resins are used to produce 25,000—100,000 t of film or sheet, and then there are a large number of high priced, high performance materials that serve niche markets. The original clear film product, ceUophane, has faUen to about 25,000 t in the United States, with only one domestic producer. Table 7 Hsts some of the principal film and sheet material manufacturers in the United States.
On the other hand, silicones are used in organic composites. The application of alloys composed of the fully cured silicone rubber particles in a continuous thermoplastic phase, called thermoplastic silicone vulcanizate, which offers high-performance materials, has been reported.506,507 Functionalized POSS was not only co-polymerized, but also blended with poly(methylmethacrylate) to study the effect of silsesquioxanes on the thermal stability of thermoplastics.508... [Pg.679]

The solution behavior has been significantly enhanced by the same structural modifications as reported previously for aromatic LC polyesters. For example poly-(p-phenylene terephthalamide) has been modified by bulky, stiff substituents [32], flexible alkyl side chains [33], the incorporation of kinked and double kinked comonomers, and comonomers of different lengths [34], as well as the use of noncoplanar bipheny-lene monomers [35]. To develop high performance materials, modifications that increase the solubility while maintaining the rod-like character, high glass transition temperatures, and the temperature stability are of particular interest. The solubility and the chain stiffness are critical factors in achieving lyotropic solutions. [Pg.22]

Bacosca I, Hamciuc E, Bruma M, Ignat M. Poly(amide imidejs containing functional nitrile groups for high performance materials. Reactive Funct Polym 2011 71(8) 905-15. [Pg.336]

The introduction of heteroaromatic units into polymer backbones has played a major role in the advancement of high performance materials. This strategy has resulted in a number of aromatic heterocyclic polymers and aromatic-heteroaromatic polyamides. For example, Marvel s preparation of polybenzimidazole or Kvenzel s work in which oxadiazole rings were incorporated in aromatic polyamides. We now report the preparation of poly(imidazoleamides), a new class of heteroaromatic polyamides based on cyanoimidazoles. [Pg.95]

Small amounts of polymer-grade terephthaHc acid and dimethyl terephthalate are used as polymer raw materials for a variety of appHcations, eg, adhesives and coatings. They are also used to make high performance polymers or engineering resins. Poly(ethylene terephthalate) is itself an engineering resin, although one more widely used is poly (butylene) terephthalate, formed by reaction with 1,4-butanediol as the comonomer. [Pg.492]

Acrylic ESTER POLYMERS Acrylonitrile POLYMERS Cellulose esters). Engineering plastics (qv) such as acetal resins (qv), polyamides (qv), polycarbonate (qv), polyesters (qv), and poly(phenylene sulfide), and advanced materials such as Hquid crystal polymers, polysulfone, and polyetheretherketone are used in high performance appHcations they are processed at higher temperatures than their commodity counterparts (see Polymers containing sulfur). [Pg.136]

Most moisture-curing liquid adhesives utilize poly(oxypropylene) (PPG) polyols, as shown above. These raw materials produce among the lowest-viscosity prepolymers but may not have sufficient modulus at higher temperatures for some applications. A certain percentage of polyester polyols may also be utilized to boost performance, but these may cause a large increase in viscosity, and so they are more often used in conjunction with polyether polyols to provide a high-performance adhesive with workable viscosities. Poly(butadiene) polyols may be utilized for specific adhesion characteristics. [Pg.782]

A wide variety of high-performance polymeric materials have been synthesized by incorporating thermally stable moieties such as sulfone, ketone, or aryl or alkyl phosphine oxide in addition to the ether linkage in poly(arylene ether)s. [Pg.329]

Poly(2,6-dimethyl-l,4-oxyphenylene) (poly(phenylene oxide), PPG) is a material widely used as high-performance engineering plastics, thanks to its excellent chemical and physical properties, e.g., a high 7 (ca. 210°C) and mechanically tough property. PPO was first prepared from 2,6-dimethylphenol monomer using a copper/amine catalyst system. 2,6-Dimethylphenol was also polymerized via HRP catalysis to give a polymer exclusively consisting of 1,4-oxyphenylene unit, while small amounts of Mannich-base and 3,5,3, 5 -tetramethyl-4,4 -diphenoquinone units are always contained in the chemically prepared PPO. [Pg.233]


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See also in sourсe #XX -- [ Pg.161 ]




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