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Methacrylate polymers, acid-containing

Polymers. The molecular weights of polymers used in high energy electron radiation-curable coating systems are ca 1,000—25,000 and the polymers usually contain acryUc, methacrylic, or fumaric vinyl unsaturation along or attached to the polymer backbone (4,48). Aromatic or aUphatic diisocyanates react with glycols or alcohol-terrninated polyether or polyester to form either isocyanate or hydroxyl functional polyurethane intermediates. The isocyanate functional polyurethane intermediates react with hydroxyl functional polyurethane and with acryUc or methacrylic acids to form reactive p olyurethanes. [Pg.428]

Block copolymers of vinyl acetate with methyl methacrylate, acryflc acid, acrylonitrile, and vinyl pyrrohdinone have been prepared by copolymeriza tion in viscous conditions, with solvents that are poor solvents for the vinyl acetate macroradical (123). Similarly, the copolymeriza tion of vinyl acetate with methyl methacrylate is enhanced by the solvents acetonitrile and acetone and is decreased by propanol (124). Copolymers of vinyl acetate containing cycHc functional groups in the polymer chain have been prepared by copolymeriza tion of vinyl acetate with A/,A/-diaIlylcyanamide and W,W-diaIl5lamine (125,126). [Pg.466]

Table VII the electron-beam exposure characteristics are given for the soluble poly (triphenylmethyl methacrylate-co-methyl methacrylate)s. The sensitivity on alkaline development was strongly influenced by the copolymer composition. The highest sensitivity was obtained on the copolymer containing 93.7 mol% methyl methacrylate. The copolymer of highest sensitivity showed the 7-value of 6.3, which was nearly twice as large as that for poly(methyl methacrylate). Formation of methacrylic acid units on exposure is obvious from the infrared spectrum. However, the mechanism of the occurrence should be different from the case of the a,a-dimethylbenzyl methacrylate polymer since there are no /3-hydrogen atoms in the triphenylmethyl group, and may be similar to the case of poly (methyl methacrylate). This will be explored in the near future. Table VII the electron-beam exposure characteristics are given for the soluble poly (triphenylmethyl methacrylate-co-methyl methacrylate)s. The sensitivity on alkaline development was strongly influenced by the copolymer composition. The highest sensitivity was obtained on the copolymer containing 93.7 mol% methyl methacrylate. The copolymer of highest sensitivity showed the 7-value of 6.3, which was nearly twice as large as that for poly(methyl methacrylate). Formation of methacrylic acid units on exposure is obvious from the infrared spectrum. However, the mechanism of the occurrence should be different from the case of the a,a-dimethylbenzyl methacrylate polymer since there are no /3-hydrogen atoms in the triphenylmethyl group, and may be similar to the case of poly (methyl methacrylate). This will be explored in the near future.
A one-sided binding of the complex to the support resulted in further improvements (92). This requires synthesis of nonsymmetric salen-type ligands, which is complicated by the tendency of such ligands to equilibrate to give mixtures containing symmetric Schiff bases. Excellent results were obtained with monomer 7d, diluted in a methacrylate polymer, by using a combination of meta-chloroperbenzoic acid (mCPBA) and A-methyl-morpholine-A-oxide (NMO) as the oxidants ... [Pg.19]

Methacrylic Acid Content in Polymer. One gram of methanol-precipitated, water-washed, dried polymer was dissolved in 100 ml. tetra-hydrofuran (THF) and titrated to a faint pink phenolphthalein end point with 0.055 n-benzyltrimethylammonium hydroxide in THF. The base was standardized by potentiometric titration against 0.01N acetic acid in methanol. The value for a non-acid containing polymer of the same series was used as a blank. All analyses were within 5% of the theoretical value. [Pg.210]

Polycarbodiimide methacrylates are obtained from the corresponding urea methacrylates. These polymers are utilized in the reaction with waterborne carboxylic acid containing acrylic polymers to produce waterborne polymers with methacrylic functonality." ... [Pg.251]

A 1 1 mixture of a carbodiimide containing latex polymer (t-butylcarbodiimidoethyl methylmethacrylate) and a carboxylic acid containing latex polymer (2-ethylhexyl methacrylate) showed that polymer interdiffusion occurs faster than crosslinking. Also, cyclohexylcarbodiimidoethyl methacrylate and t-butylcarbodiimidoethyl methacrylate have been prepared, and these monomers are used to prepare carbodiimide functionalized latex particles for emulsion polymerization. ... [Pg.254]

Examples of acid modified polyolefins are the copolymers of ethylene with acrylic acid or methacrylic acid. Variations include the partially neutralised acid copolymers with metal ions (ionomers) or terpolymers of ethylene, an acid and an acrylate such as methyl acrylate or isobutyl acrylate. Acid-containing extrudable adhesives are widely used to bond to aluminium foil. Examples of anhydride-modified polyolefins include terpolymers of ethylene, maleic anhydride and acrylates such as ethyl acrylate or butyl acrylate and the anhydride-grafted polyolefins. Some typical applications and stmctures of a variety of multilayer materials with extruded polymer tie-layer adhesives, as described in Du-Pont trade literature, are detailed in Table 16.2. [Pg.350]

A soft contact lens comprises a water-swollen gel of a polymer prepared by polymerising one or more hydrophilic monomers, such as 2-hydroxyethyl methacrylate, one or more crosslinking monomers and a monomer, which contains metal-chelating functionality, such as an aminopolycarboxylic acid containing a polymerisable olefinic group. [Pg.98]

Promising positive-tone bilayer resists based on silicon-containing methacrylate polymers bearing acid labile side groups (Scheme 7.49), and designed for ArF lithography, were reported in 1996 by researchers at Olin Ceiba-Geigy... [Pg.394]


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See also in sourсe #XX -- [ Pg.303 ]




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Acid-containing polymers

Acids containing

Acids methacrylic acid

METHACRYLATE POLYMER

Methacrylate-containing polymers

Methacrylic acid

Methacrylic acid methacrylate

Polymer acid

Polymers, methacrylates

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