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Polyurethanes acrylate substituted

Polyurethanes have also been invaluable as coatings for textiles, paper, and leather. The ability of these lacquers to adhere to a wide variety of substrates, combined with the flexibility across a wide range of temperatures and high tensile strength and tear propagation resistance, makes PU coated materials attractive substitutes for PVC, nitrocellulose, and acrylates. ... [Pg.2377]

It is very clear that if the initiator has hydroxyl groups, and if the termination takes place exclusively by recombination then a polymeric diol is obtained [2, 3], which is ideal for polyurethane. If the termination takes place by disproportionation, only monofunctional compounds are obtained, which cannot be used in PU. The vinylic and dienic monomers used in practice have various termination mechanisms. Some monomers give only recombination reactions, such as styrene, acrylates (methyl acrylate, ethyl acrylate, butyl acrylate, 2-ethyl hexyl acrylate), acrylonitrile and butadiene. Other monomers give both mechanisms of termination, around 65-75% disproportionation and 25-35% recombination, such as methacrylates (methyl methacrylate, ethyl methacrylate, butyl methacrylate etc.), substituted styrenes and other monomers [2, 3, 4]. [Pg.296]

Water-reducible polyunsaturated acid substituted aqueous polyurethane dispersions are also being used (40). They can be made by reacting a diisocyanate with a polyol, monoglyceride of a drying oil, and dimethylolpropionic acid. The carboxylic acid groups are neutralized with a tertiary amine and dispersed in water. If aliphatic isocyanates are used, good color retention can be obtained. They are much more resistant to hydrolysis than conventional alkyd resins. Films also have excellent abrasion resistance. Cost can be reduced by blending in 10-20% of acrylic latex. [Pg.448]

Thermal stability measurements have been carried out on numerous other polymers including polyethylene ethylene vinyl-alcohol copolymer [12], polyaniline [13], ) 3 s-stilbene-N-substituted maleimides [14], cellulose [15-20], polystyrene [14, 16], ethylene-styrene copolymers [21,22], ST-DVB-based ion exchangers [23], vinyl chloride-acrylonitrile copolymers [24], polyethylene terephthalate [25], polyesters such as polyisopropylene carboxylate [26], polyglycollate [27-29], Nylon 6 [30], polypyromellitimides, poly-N-a-naphthylmaleimides [26,31], polybenzo-bis(amino-imino pyrolenes) [32], polyvinyl chloride [33-35], acrylamide-acrylate copolymers and polyacrylic anhydride [36-38], polyamides [39], amine-based polybenzo-oxazines [40], polyester hydrazides [41], poly-a-methyl styrene tricarbonyl chromimn [42], polytetrahydrofuran [43], polyhexylisocyanate [44], polyurethanes [45], ethylene-... [Pg.40]

Tg measurements have been performed on many other polymers and copolymers including phenol bark resins [71], PS [72-74], p-nitrobenzene substituted polymethacrylates [75], PC [76], polyimines [77], polyurethanes (PU) [78], Novolac resins [71], polyisoprene, polybutadiene, polychloroprene, nitrile rubber, ethylene-propylene-diene terpolymer and butyl rubber [79], bisphenol-A epoxy diacrylate-trimethylolpropane triacrylate [80], mono and dipolyphosphazenes [81], polyethylene glycol-polylactic acid entrapment polymers [82], polyether nitrile copolymers [83], polyacrylate-polyoxyethylene grafts [84], Novolak type thermosets [71], polyester carbonates [85], polyethylene naphthalene, 2,6, dicarboxylate [86], PET-polyethylene 2,6-naphthalone carboxylate blends [87], a-phenyl substituted aromatic-aliphatic polyamides [88], sodium acrylate-methyl methacrylate multiblock copolymers [89], telechelic sulfonate polyester ionomers [90], aromatic polyamides [91], polyimides [91], 4,4"-bis(4-oxyphenoxy)benzophenone diglycidyl ether - 3,4 epoxycyclohexyl methyl 3,4 epoxy cyclohexane carboxylate blends [92], PET [93], polyhydroxybutyrate [94], polyetherimides [95], macrocyclic aromatic disulfide oligomers [96], acrylics [97], PU urea elastomers [97], glass reinforced epoxy resin composites [98], PVOH [99], polymethyl methacrylate-N-phenyl maleimide, styrene copolymers [100], chiral... [Pg.97]


See other pages where Polyurethanes acrylate substituted is mentioned: [Pg.2031]    [Pg.625]    [Pg.350]    [Pg.183]    [Pg.65]    [Pg.495]    [Pg.259]    [Pg.212]    [Pg.283]    [Pg.58]    [Pg.764]    [Pg.25]    [Pg.32]    [Pg.128]    [Pg.147]    [Pg.858]    [Pg.878]    [Pg.1049]    [Pg.1059]    [Pg.626]    [Pg.154]    [Pg.238]    [Pg.29]    [Pg.8695]    [Pg.317]    [Pg.345]    [Pg.39]    [Pg.233]   
See also in sourсe #XX -- [ Pg.189 ]




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Polyurethane acrylated

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