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Polysiloxanes Polysulfones

The more certain approach leading to products in which the different component species must necessarily alternate along the chain is that involving the combination of two oligomers having mutually reactive end groups such that each species can react only with the other (equation 7). This procedure, which has been used particularly in recent work on polycarbonate-polysulfone and polysiloxane-polysulfone block copolymers, yields multiblock products with structures defined... [Pg.1142]

Polymerization Solvent. Sulfolane can be used alone or in combination with a cosolvent as a polymerization solvent for polyureas, polysulfones, polysiloxanes, polyether polyols, polybenzimidazoles, polyphenylene ethers, poly(l,4-benzamide) (poly(imino-l,4-phenylenecarbonyl)), silylated poly(amides), poly(arylene ether ketones), polythioamides, and poly(vinylnaphthalene/fumaronitrile) initiated by laser (134—144). Advantages of using sulfolane as a polymerization solvent include increased polymerization rate, ease of polymer purification, better solubilizing characteristics, and improved thermal stability. The increased polymerization rate has been attributed not only to an increase in the reaction temperature because of the higher boiling point of sulfolane, but also to a decrease in the activation energy of polymerization as a result of the contribution from the sulfonic group of the solvent. [Pg.70]

Copolymers. Copolymers from mixtures of different bisphenols or from mixtures of dichlorosulfone and dichlorobenzophenone have been reported in the patent literature. Bifunctional hydroxyl-terminated polyethersulfone oligomers are prepared readily by the polyetherification reaction simply by providing a suitable excess of the bisphenol. Block copolymers are obtained by reaction of the oligomers with other polymers having end groups capable of reacting with the phenol. Multiblock copolymers of BPA-polysulfone with polysiloxane have been made in this way by reaction with dimethyl amino-terminated polydimethylsiloxane the products are effective impact modifiers for the polyethersulfone (79). Block copolymers with nylon-6 are obtained when chlorine-terminated oligomers, which are prepared by polyetherification with excess dihalosulfone, are used as initiators for polymerization of caprolactam (80). [Pg.332]

The specialty resins are expensive, produced in relatively small volumes either for a specific application or looking for a market niche. Their Tg > 200°C and modulus > 3 GPa. In 1991 the total world consumption of polysulfones (PSE) and polyethersulfones (PES) was 8.5 kton. Blends of the following polymers are known polyfluorocarbons, polysiloxanes, sulfur-containing polymers (PPS, PPSS, PES, and PSF), polyetherk-etones (PEK, PEEK, PEKK), polyimides (PI, PEI, and PAI), PAr, COPO, polyphosphazene (PHZ) and LCP. [Pg.80]

The cellulose based materials that are used as nano-reinforcements are cellulose nanocrystals (i.e. whiskers and nanospheres), nanofibrillated cellulose, regenerated cellulose nanoparticles and electrospun nanofibers. A wide range of polymer matrices have been used to form cellulose nanocomposites. Synthetic polymers such as polypropylene, poly(vinyl chloride) (PVC) [102], waterborne epoxy [103], waterborne polyurethane [104], polyurethane [105], poly-(styrene-co-butyl acrylate) [106], poly(oxyethylene) [107], polysiloxanes [108], polysulfonates [109], cellulose acetate butyrate [110,111], poly(caprolactone) [112], poly(viny 1 alcohol) [113] and poly (vinyl acetate) [114]. Different biopolymers such as starch-based... [Pg.34]

A series of patents were issued to Mammino on various resins like modified polysulfones and polysiloxanes that can be photocrosslinked when Lewis acids are added. In addition, light sensitive polysulfone copolymers can be formed through interfacial polycondensation. " Also, the reactions can be carried out on mixed bisphenols and aromatic disulfonyl chlorides in the presence of Lewis acids. [Pg.237]

Sulfolane is used as a polymerization solvent for the production of polysulfones, polysiloxanes, polyphenylene ethers, and other polymers. Sulfolane is said to increase the reaction rates, afford easier polymer purification, and improved thermal stability. Sulfolane is a solvent for dissolving a variety of polymers for use in the fiber-spinning process. Cellulose and cellulose ester polymers can be plasticized with sulfolane to give improved flexibility and other physical property improvements [12,13]. Other application areas that have used sulfolane include electronic and electrical, textile-dye uses, curing of polysulfide sealant, and as a catalyst in certain synthetic reactions. [Pg.287]

Polyolefins Polystyrenes Polyacrylates Polymethacrylates Polyacrylonitriles Polyacrylamides Poly(vinyl halides) Poly(vinylidene halides) Poly(vinyl ethers) Poly(vinyl ketones) Poly(vinyl esters) Poly(vinyl pyridines) Polydienes Polyethers Polyesters, aliphatic Polyesters, aromatic Polyamides Polysiloxanes Polyphosphazenes Polysulfones... [Pg.422]

Silanol, bivalent radical-, polysiloxane Cyclic sulfone, polysulfone... [Pg.16]


See other pages where Polysiloxanes Polysulfones is mentioned: [Pg.332]    [Pg.11]    [Pg.664]    [Pg.95]    [Pg.188]    [Pg.234]    [Pg.54]    [Pg.370]    [Pg.347]    [Pg.187]    [Pg.216]    [Pg.217]    [Pg.850]    [Pg.623]    [Pg.242]    [Pg.243]    [Pg.67]    [Pg.204]    [Pg.15]    [Pg.203]    [Pg.122]    [Pg.628]    [Pg.112]    [Pg.317]    [Pg.370]   
See also in sourсe #XX -- [ Pg.26 ]




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Polysiloxane

Polysiloxanes

Polysulfones

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