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Polycarbonate polyester

Quenched sheet is pulled horizontally from the stack and is then either wound on roUs or sheared into sheets of the required dimension. Among the polymers made into sheet this way are the polyolefins, poly(vinyl chloride), amorphous polyester, polycarbonate, and polyarjiate. [Pg.379]

Poly(ethylene carbonate). Like polyesters, polycarbonates (qv) are bioabsorbable only if the hydrolyzable linkages are accessible to enzymes and/or water molecules. Thus pellets of poly(ethylene carbonate), ( OCOOCH2CH2 )n weighing 200 mg implanted ia the peritoneal cavity of rats,... [Pg.191]

Polypropylene sheet has been used most extensively however, thermoplastic polyester, polycarbonate, and nylon versions are available (see Elastomers, synthetic Polycarbonates). Continuous strand glass fiber mat is the typical reinforcement. The limited number of sheet suppHers reduces potential for competitive pricing. [Pg.96]

Another recent development is the preparation of a polyester-polycarbonate copolymer. The polymers involve a polyester component based on the reaction between bis-phenol A and iso- or terephthalic acid with the carbonate component arising from the reactions described in Section 20.3 (see Section 20.9). [Pg.566]

Hydrolysis studies compared a polycarbonate urethane with a poly(tetramethyl-ene adipate) urethane and a polyether urethane based on PTMEG. After 2 weeks in 80°C water, the polycarbonate urethane had the best retention of tensile properties [92], Polycarbonates can hydrolyze, although the mechanism of hydrolysis is not acid-catalyzed, as in the case of the polyesters. Polycarbonate polyurethanes have better hydrolysis resistance than do standard adipate polyurethanes, by virtue of the highest retention of tensile properties. It is interesting to note in the study that the PTMEG-based urethanes, renowned for excellent hydrolysis resistance, had lower retention of physical properties than did the polycarbonate urethanes. [Pg.808]

Polyolefines, polyesters, polycarbonates, polystyrene, polysulphone, polysulphone, polyphenylene oxide and polymethylinethacrylate... [Pg.952]

Nearly all of the polymers produced by step-growth polymerization contain heteroatoms and/or aromatic rings in the backbone. One exception is polymers produced from acyclic diene metathesis (ADMET) polymerization.22 Hydrocarbon polymers with carbon-carbon double bonds are readily produced using ADMET polymerization techniques. Polyesters, polycarbonates, polyamides, and polyurethanes can be produced from aliphatic monomers with appropriate functional groups (Fig. 1.1). In these aliphatic polymers, the concentration of the linking groups (ester, carbonate, amide, or urethane) in the backbone greatly influences the physical properties. [Pg.4]

Many random copolyesters and polyester-polycarbonates have also been prepared by ester interchange reactions in the molten state. Thus, poly(ethylene terephthalate-co -isophthalates) can be obtained by simple melt blending of PET and poly(ethylene isophthalate) (PEI) homopolyesters at 270°C. The copolymer changes gradually from a block type at the beginning of reaction to a random-type... [Pg.89]

Other reports on the morphology and mechanical behavior of organosiloxane containing copolymeric systems include polyurethanes 201 202), aliphatic 185, 86) and aromatic117,195> polyesters, polycarbonates 233 236>, polyhydroxyethers69,311, siloxane zwitterionomers 294 295) and epoxy networks 115>. All of these systems display two phase morphologies and composition dependent mechanical properties, as expected. [Pg.68]

Many of the commercially important plastics such as polystyrene, polyamide, polyester, polycarbonate, polysulfone, polyphenylene oxide alloys, epoxy, and phenolics lack good impact... [Pg.329]

Oxidoreductases Transferases Hydrolases Lyases Isomerases Ligases Phenolic polymers, polyanilines, vinyl polymers Polysaccharides, cyclic oligosaccharides, polyesters Polysaccharides, polyesters, polycarbonates, poly(amino acid)s, polyphosphates... [Pg.206]

Enzymes are generally classified into six groups. Table 1 shows typical polymers produced with catalysis by respective enzymes. The target macromolecules for the enzymatic polymerization have been polysaccharides, poly(amino acid)s, polyesters, polycarbonates, phenolic polymers, poly(aniline)s, vinyl polymers, etc. In the standpoint of potential industrial applications, this chapter deals with recent topics on enzymatic synthesis of polyesters and phenolic polymers by using enzymes as catalyst. [Pg.206]

Co-extrusion with polyamides, polypropylene, polyethylene, EVA, thermoplastic polyester, polycarbonate, polystyrene, ionomers for packaging of fertilizers, herbicides and other chemicals. [Pg.150]

Most polyester alloys are polyester/polycarbonates and properties, processability and prices are intermediate between those of polyester and polycarbonate. A few alloys are poly-ester/ASA and properties, processability and prices are intermediate between those of polyester and ASA. [Pg.633]

Among the plastics suitable for blow moulding are polyethylenes, polypropylenes, polyacrylonitrile, thermoplastic polyesters, polycarbonates... [Pg.724]

There are numerous bifunctional monomers used in condensation polymerization. Some of the more popular signature groups that turn up frequently are shown in Figure 22-3. Important copolymers made by condensation include epoxies, nylon, polyesters, polycarbonate, and polyimides. As always, there are exceptions, and one is Nylon 6 made by a ring opening reaction of caprolactam. All of these will be covered in the next two chapters. [Pg.326]

Interfacially formed condensation polymers such as polyesters, polycarbonates, nylons, and PUs are typically formed on a microscopic level in a chain-growth manner largely because of the highly reactive nature of the reactants employed for such interfadal polycondensations. [Pg.88]

Extension of DKR to polymer chemistry would readily result in chiral polyesters, polycarbonates, or polyamides from an optically inactive monomer mixture. Scheme 10 describes three variants of chemoenzymatic catalysis applied in polymer chemistry that recently appeared in the literature. Route A uses AA and BB monomers to prepare chiral polymers from racemic/diasteromeric diols. Route B converts an enantiomer mixture of AB monomers to homochiral polymers. Route C is the enzymatic ring-opening polymerization of co-methylated lactones to homochiral polyesters. Details will be given in Sect. 3.4.2. [Pg.103]

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. [Pg.539]

Polymers are large molecules (macromolecules) that consist of one or two small molecules (monomers) joined to each other in long, often highly branched, chains in a process called polymerization. Both natural and synthetic polymers exist. Some examples of natural polymers are starch, cellulose, chitin (the material of which shells are made), nucleic acids, and proteins. Synthetic polymers, the subject of this chapter, include polyethylene, polypropylene, polystyrene, polyesters, polycarbonates, and polyurethanes. In their raw, unprocessed form, synthetic polymers are sometimes referred to as resins. Polymers are formed in two general ways by addition or by condensation. [Pg.151]

Essentially polymer-film capacitors comprise dielectric films (polymer or paper or both together) interleaved with aluminium electrodes, either as aluminium foil or, more commonly, in the form of a layer evaporated directly on the dielectric, and rolled together. They are sealed in an aluminium can or in epoxy resin. Because the dielectric films and evaporated electrodes have thicknesses of only a few microns and about 0.025 /mi respectively, volumetric efficiencies can be high. The dielectric films are polystyrene, polypropylene, polyester, polycarbonate or paper paper dielectrics are always impregnated with an insulating liquid. [Pg.257]

Interfaciarpolymerization can be used to make many types of step-growth polymers such as polyamides, polyesters, polycarbonates, and polyurethanes. Although most step-growth polymers are prepared by a melt process, somd specialty polymers are prepared by the interfacial technique, allowing rapid reaction at low temperatures. [Pg.92]

Condensation polymers result from formation of ester or amide linkages between difunctional molecules. Condensation polymerization usually proceeds by step-growth polymerization, in which any two monomer molecules may react to form a dimer, and dimers may condense to give tetramers, and so on. Each condensation is an individual step in the growth of the polymer, and there is no chain reaction. Many kinds of condensation polymers are known. We discuss the four most common types polyamides, polyesters, polycarbonates, and polyurethanes. [Pg.1232]

Color Dye Chemical Type Acetal Nylon Cellulosic Polyester Polycarbonate Fluoropolymer... [Pg.183]

The segmented polyamide elastomers are synthesized from MDI (4,4 -diisocyanato-diphenylmethane) and dicarboxylic acids and a carboxylic acid terminated aliphatic polyester, polycarbonate or polyether prepolymer with an average molecular weight of M = 500-5000. The dicarboxylic acids used as hard segment extenders are adipic and azelaic acid. Also, poly(ester amide) alloys are obtained using nylon-6,6 or polyesters (PEA/PBT). [Pg.269]

The plastics industry and all the products made from plastics are almost entirely dependent on chemicals extracted or produced from hydrocarbons. This includes not only the familiar materials such as polyethylene, polypropylene, polyvinyl chloride (PVC), epoxies, nylon, polyesters, polycarbonate. Teflon and Plexiglas, but also includes a large portion of materials made from rubber and a diverse group of other materials formulated from polymers such as tape, glue, ink, waterproofing, wax, and polishes. Virtually all the synthetic fibers used in textile products, Orion , Dacron , Nylon and polyesters are made from polymers based on hydrocarbons. [Pg.24]

Generally, the contribution of intermolecular attractive forces operating within PUR end products increases in the order polyethers < polyesters < polycarbonates or polyanhydrides. [Pg.198]


See other pages where Polycarbonate polyester is mentioned: [Pg.479]    [Pg.539]    [Pg.602]    [Pg.3]    [Pg.47]    [Pg.241]    [Pg.294]    [Pg.621]    [Pg.56]    [Pg.59]    [Pg.3]    [Pg.185]    [Pg.261]    [Pg.507]    [Pg.125]    [Pg.349]    [Pg.252]    [Pg.252]    [Pg.451]    [Pg.9]   
See also in sourсe #XX -- [ Pg.96 ]

See also in sourсe #XX -- [ Pg.16 ]

See also in sourсe #XX -- [ Pg.96 ]




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Polycarbonate polyester dependence

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Polycarbonate polyester monomers

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