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Methacrylic acid esters

In these equations I is the initiator and I- is the radical intermediate, M is a vinyl monomer, I—M- is an initial monomer radical, I—M M- is a propagating polymer radical, and and are polymer end groups that result from termination by disproportionation. Common vinyl monomers that can be homo-or copolymeri2ed by radical initiation include ethylene, butadiene, styrene, vinyl chloride, vinyl acetate, acrylic and methacrylic acid esters, acrylonitrile, A/-vinylirnida2ole, A/-vinyl-2-pyrrohdinone, and others (2). [Pg.219]

Polymeric dimethylbutadiene peroxide Polymeric peroxides of methacrylic acid esters and styrene... [Pg.238]

Dimethyl peroxide Diethyl peroxide Di-t-butyl-di-peroxyphthalate Difuroyl peroxide Dibenzoyl peroxide Dimeric ethylidene peroxide Dimeric acetone peroxide Dimeric cyclohexanone peroxide Diozonide of phorone Dimethyl ketone peroxide Ethyl hydroperoxide Ethylene ozonide Hydroxymethyl methyl peroxide Hydroxymethyl hydroperoxide 1-Hydroxyethyl ethyl peroxide 1 -Hydroperoxy-1 -acetoxycyclodecan-6-one Isopropyl percarbonate Isopropyl hydroperoxide Methyl ethyl ketone peroxide Methyl hydroperoxide Methyl ethyl peroxide Monoperoxy succinic acid Nonanoyl peroxide (75% hydrocarbon solution) 1-Naphthoyl peroxide Oxalic acid ester of t-butyl hydroperoxide Ozonide of maleic anhydride Phenylhydrazone hydroperoxide Polymeric butadiene peroxide Polymeric isoprene peroxide Polymeric dimethylbutadiene peroxide Polymeric peroxides of methacrylic acid esters and styrene... [Pg.163]

W. Ritter, C. Meyer, W. Zollner, C. P. Herold, and S. von Tapavicza. Use of selected acrylic and/or methacrylic acid ester copolymers as flow enhancers in paraffin-rich crude oil and crude oil fraction (II) (Verwendung ausgewahlter Copolymeren der Acryl- und/oder Methacrylsaureester als FlieBverbesserer in paraffinreichen Erdolen und Erdolfraktionen [II]). Patent EP 332002,1989. [Pg.452]

Oberly R, Tansy MF LC50 values for rats acutely exposed to vapors of acrylic and methacrylic acid esters, jf Toxicol Environ Health 16 811, 1985... [Pg.101]

To the first category belong the homo- and copolymerization of macromonomers. For this purpose, macromolecules with only one polymerizable end group are needed. Such macromonomers are made, for example, by anionic polymerization where the reactive chain end is modified with a reactive vinyl monomer. Also methacrylic acid esters of long-chain aliphatic alcohols or monofunctional polyethylene oxides or polytetrahydrofurane belong to the class of macromonomers. [Pg.257]

Was used in prepn of acrylate resins and of other copolymers and polymers. Acrylate resins are thermoplastic polymers or polymers of acrylic and methacrylic acid, esters of these acids or acrylonitrile. Acrylic acid acrylonitrile and their derivatives are described in Vol 1 of Encycl, pp A96-R A97. Methacrylic acid is a-methylacrylic acid,... [Pg.181]

Many of these newer materials have become standard polymers for inclusion in the cooling water formulations from most service companies. There are even tetrapolymers available now (for example, acrylic acid, methacrylic acid, ester, acrylamide, or AA/MAA/E/AM). [Pg.153]

Simple diastereoselectivity may also occur in Diels-Alder reactions between electron-poor dienophiles and cyclopentadiene (Figure 15.30). Acrylic acid esters or fraus-crotonic acid esters react with cyclopentadiene in the presence or absence of A1C13 with substantial selectivity to afford the so-called emfo-adducts. When the bicyclic skeleton of the main product is viewed as a roof the prefix endo indicates that the ester group is below this roof, rather than outside (exo). However, methacrylic acid esters add to cyclopentadiene without any exo.endo-selectivity regardless whether the reaction is carried out with or without added A1C13 (Figure 15.30, bottom). [Pg.669]

Methacrylic acid esters Non ionic Hydrophilic monomers for Alkyl can be... [Pg.206]

Copolymers with methacrylic acid esters are also used in packaging. [Pg.29]

PVC can be blended with numerous other polymers to give it better processability and impact resistance. For the manufacture of food contact materials the following polymerizates and/or polymer mixtures from polymers manufactured from the above mentioned starting materials can be used Chlorinated polyolefins blends of styrene and graft copolymers and mixtures of polystyrene with polymerisate blends butadiene-acrylonitrile-copolymer blends (hard rubber) blends of ethylene and propylene, butylene, vinyl ester, and unsaturated aliphatic acids as well as salts and esters plasticizerfrec blends of methacrylic acid esters and acrylic acid esters with monofunctional saturated alcohols (Ci-C18) as well as blends of the esters of methacrylic acid butadiene and styrene as well as polymer blends of acrylic acid butyl ester and vinylpyrrolidone polyurethane manufactured from 1,6-hexamethylene diisocyanate, 1.4-butandiol and aliphatic polyesters from adipic acid and glycols. [Pg.31]

For food contact articles made from acrylic and methacrylic acid ester copolymers and their polymer blends, the following starting materials can be used ... [Pg.34]

The following substances are recommended starting materials for unsaturated polyesters fumaric acid, maleic acid, methacrylic acid, adipic acid, phthalic acid, resi-nic acid, isophthalic acid, terephthalic acid, hydrated or halogenated phthalic acids, aliphatic and substituted aliphatic single and multi-functional alcohols up to C)8, alkoxylated and hydrated phenols and bisphenols, styrene, vinyltoluene, acrylic acid and methacrylic acid esters of the Ci-C4 alcohols, and tricyclodecane dimethanol. [Pg.37]

Natural rubber, graft copolymers of natural rubber with acrylic or methacrylic acid esters of mono-functional CiC4 alcohols butadiene and isoprene polymers polymers... [Pg.39]

Alkyd and polyester resins, epoxy compounds, phenol-formaldehyde resin, urea and/or melamine-aldehyde resin, cyclic urea resin, carbamide acid ester formaldehyde resin, ketone formaldehyde resin, polyurethane, polyvinylester, polyvinyl acetate, polyvinyl chloride and polymer mixtures, polyethylene, polystryrene, styrene mixtures and graft copolymers, polyamide, polycarbonate, polyvinyl ether, polyacrylic and methacrylic acid esters, polyvinyl flouride, polyvinylidene chloride copolymers, UV and/or electron irradiated lacquers. [Pg.45]

Vinyl lacquers are used mainly where a high degree of chemical resistance is required these lacquers are based on vinyl chlorides and vinyl acetates. Acrylic lacquers are based on methyl methacrylate and methyl acrylate polymers and copolymers. Other esters of acrylic and methacrylic acid also may be used to make nonconvertible film formers. Judicious selection of these acrylic acid or methacrylic acid esters allows one to produce film formers with specifically designed properties such as hardness, flexibility, gloss, durability, heat, and chemical resistance. Acrylic lacquers, however, are not noted for their water resistance. The principal uses of acrylic-type lacquers are fluorescent and metallic paints, car refinish applications, clear lacquers and sealers for metals, and protective coatings for aircraft components and for vacuum-deposited metals, as well as uses in pigmented coatings for cabinets and appliances. [Pg.1309]

Similar effects are found in the enantiomer-differentiating polymerization of oligomers (ji r 30) of chiral, sterically crowded methacrylic acid esters E. Yashima, Y. Okamoto, K. Hatada, Macromolecules 1988, 21, 854. [Pg.335]

The USPNF 23 describes methacrylic acid copolymer as a fully polymerized copolymer of methacrylic acid and an acrylic or methacrylic ester. Three types of copolymers, namely Type A, Type B, and Type C, are defined in the monograph. They vary in their methacrylic acid content and solution viscosity. Type C may contain suitable surface-active agents. Two additional polymers, Type A (Eudragit RE) and Type B (Eudragit RS), also referred to as ammonio methacrylate copolymers, consisting of fully polymerized copolymers of acrylic and methacrylic acid esters with a low content of quaternary ammonium groups, are also described in the USPNF 23. A further monograph for an aqueous dispersion of Type C methacrylic acid copolymer is also defined see Section 9. [Pg.553]

Polymethacrylates are synthetic cationic and anionic polymers of dimethylaminoethyl methacrylates, methacrylic acid, and methacrylic acid esters in varying ratios. Several different types are commercially available and may be obtained as the dry powder, as an aqueous dispersion, or as an organic solution. A (60 40) mixture of acetone and propan-2-ol is most commonly used as the organic solvent. See Tables I and III. [Pg.554]

Eudragit E is cationic polymer based on dimethylaminoethyl methacrylate and other neutral methacrylic acid esters. It... [Pg.554]

Eudragit NE 30 D and Eudragit NE 40 D are aqueous dispersions of a neutral copolymer consisting of poly-methacrylic acid esters. The dispersions are milky-white liquids of low viscosity and have a weak aromatic odor. Films prepared from the lacquer swell in water, to which they become permeable. Thus, films produced are insoluble in water, but give pH-independent drug release. [Pg.557]


See other pages where Methacrylic acid esters is mentioned: [Pg.259]    [Pg.210]    [Pg.427]    [Pg.97]    [Pg.554]    [Pg.1450]    [Pg.126]    [Pg.210]    [Pg.229]    [Pg.126]    [Pg.159]    [Pg.46]    [Pg.46]    [Pg.46]    [Pg.556]    [Pg.557]    [Pg.477]   
See also in sourсe #XX -- [ Pg.669 ]




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Acids methacrylic acid

Esters methacrylate

Esters methacrylic

Esters of acrylic and methacrylic acid

Methacrylic acid

Methacrylic acid 6- hexyl ester

Methacrylic acid methacrylate

Methacrylic acid, a-phenylthiomethyl ester

Methacrylic acid, a-phenylthiomethyl ester Michael addition

Methacrylic acid, methyl ester

Methyl ester of methacrylic acid

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