Polymers, methacrylates epoxide functionalized

A number of hydroxylated water soluble polymers were examined as coreactants with polymer 52 in the absence of calcium alginate, and were judged on the basis of the rate of gel formation and the physical properties of the gel These polymers included sodium alginate, polyvinyl alcohol, and copolymers of HEMA with MAA. Of the polymers tested, best results were obtained with polymer 10a, a copolymer of HEMA with a mole fraction of about 10% MAA, which rapidly produced an elastic gel on exposure to polymer 52 in solution. Simple condensation of the carboxyls in polymer 10a with the epoxide functionality was ruled out as a competing reaction due to the measurable but slow reaction between polymer 52 and poly methacrylic acid. It is, therefore, likely... 

Various approaches have been undertaken for reactive compatibilization of poly-amide/ABS alloys. Maleic anhydride can be grafted to the ABS. Styrene maleic anhydride (SMA) copolymers have been employed as compatibilizers for polyamide/ABS blends. SMA and SAN copolymers are miscible when the AN and maleic anhydride (MA) contents are equal. The impact strength of these blends has been found to be sensitive to the amount and composition of the SMA copolymer. Addition of SMA to SAN/polyamide blends was found to enhance the tensile and impact properties of these blends. Imidized acrylic polymers have been used as compatibilizers for nylon-6/ABS blends. Glycidyl methacrylate and methyl methacrylate (GMA/MMA) copolymers are used as compatibilizing agents. The epoxide functionality in GMA is capable of reaction with polyamide end groups. GMA/MMA copolymers can be shown to be miscible with SAN over the range of AN content of ABS. Styrene/GMA copolymers have been reported to be used as compatibilizers for polymer pairs such as... 

Chlorinated, sulfonated, chlorosulfonated or epoxidized polymers, homopolymers and copolymers of functionalized monomers, e.g. poly(methacryl aldehyde), poly(2,3-epoxypropyl acrylate), poly(4-vinylphenol), poly(propylene-co-10-unde-cene-l-ol), poly(butadiene-co-methacryl aldehyde), poly(butadiene-co-acrylic acid), poly(ethylene-co-alkyl acrylate), poly(alkyl acrylate-co-2,3-epoxypropyl acrylate), poly(alkyl acrylate-co-maleic anhydride), poly(styrene-co-4-vinylbenzyl chloride)... 

Many authors elucidated functionalization of polymers containing reactive oxirane moieties. Epoxidized NR, BR, IR and/or the respective model hydrocarbons, poly (butadiene-co-isoprene, various epoxy resins, poly (2,3-epoxypro-pyl methacrylate) and its copolymers or grafted systems were mostly exploited. Stabilizers based on epoxidized unsaturated rubbers are of the top interest. The mechanism of the functionalization process was studied in details by means of 3,4-epoxy-4-methylheptane and 1,2-epoxy-3-ethyl-2-methylpentane as model compounds [289]. The ring opening of the asymmetric oxirane is regiospecific. Aliphatic primary amines attack the least substituted carbon atom and can be involved in crosslink formation. Aromatic primary and secondary amines are less reactive than aliphatic ones because of their lower basicity the attack on the least substituted carbon atom is however preferred too. 

Vinyl-functional alkylene carbonates can also be prepared from the corresponding epoxides in a manner similar to the commercial manufacture of ethylene and PCs via CO2 insertion. The most notable examples of this technology are the syntheses of 4-vinyl-1,3-dioxolan-2-one (vinyl ethylene carbonate, VEC) (5, Scheme 24) from 3,4-epoxy-1-butene or 4-phenyl-5-vinyl-l,3-dioxolan-2-one (6, Scheme 24) from analogous aromatic derivative l-phenyl-2-vinyl oxirane. Although the homopolymerization of both vinyl monomers produced polymers in relatively low yield, copolymerizations effectively provided cyclic carbonate-containing copolymers. It was found that VEC can be copolymerized with readily available vinyl monomers, such as styrene, alkyl acrylates and methacrylates, and vinyl esters.With the exception of styrene, the authors found that VEC will undergo free-radical solution or emulsion copolymerization to produce polymeric species with a pendant five-membered alkylene carbonate functionality that can be further cross-linked by reaction with amines. Polymerizations of 4-phenyl-5-vinyl-l,3-dioxolan-2-one also provided cyclic carbonate-containing copolymers. 

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