Methyl acrylate, copolymers with methacrylate

An example of this improvement in toughness can be demonstrated by the addition of Vamac B-124, an ethylene/methyl acrylate copolymer from DuPont, to ethyl cyanoacrylate [24-26]. Three model instant adhesive formulations, a control without any polymeric additive (A), a formulation with poly(methyl methacrylate) (PMMA) (B), and a formulation with Vamac B-124 (C), are shown in Table 4. The formulation with PMMA, a thermoplastic which is added to modify viscosity, was included to determine if the addition of any polymer, not only rubbers, could improve the toughness properties of an alkyl cyanoacrylate instant adhesive. To demonstrate an improvement in toughness, the three formulations were tested for impact strength, 180° peel strength, and lapshear adhesive strength on steel specimens, before and after thermal exposure at 121°C. 

Glycidyl methacrylate has also been grafted to polyethylene and to poly(ethylene-co-propylene) using peroxides in extruders.87 The reactive group need not be pendant. It can be part of a copolymer. Ethylene-methyl acrylate copolymers and styrene-maleic anhydride copolymers have been reacted with ammonia and with amines in extruders.88... 

In order to achieve high local concentrations of antibiotics in infected bone or joint, methyl methacrylate/ methyl acrylate copolymer (PMMA) bead chains or minichains loaded with an antibiotic (mostly gentamicin sulfate) are inserted. 

Important copolymers of styrene are SBR (styrene butadiene rubbers), ABS, a copolymer with butadiene and acrylonitrile, and various copolymers with methacylic and acrylic esters, such as styrene-methyl methacrylate and styrene-methyl acrylate copolymers. Additionally, copolymers formed with one or more of the following monomers also exist ethylene, a-methyl styrene, vinyl acetate, maleic anhydride, and acrylonitrile. 

Numerous recipes have been pubUshed, primarily ia the patent Hterature, that describe the preparation of acrylate and methacrylate homopolymer and copolymer dispersions (107,108). A typical process for the preparation of a 50% methyl methacrylate, 49% butyl acrylate, and 1% methacrylic acid terpolymer as an approximately 45% dispersion ia water begias with the foUowiag charges ... 

The uniqueness of methyl methacrylate as a plastic component accounts for its industrial use in this capacity, and it far exceeds the combined volume of all of the other methacrylates. In addition to plastics, the various methacrylate polymers also find appHcation in sizable markets as diverse as lubricating oil additives, surface coatings (qv), impregnates, adhesives (qv), binders, sealers (see Sealants), and floor poHshes. It is impossible to segregate the total methacrylate polymer market because many of the polymers produced are copolymers with acrylates and other monomers. The total 1991 production capacity of methyl methacrylate in the United States was estimated at 585,000 t/yr. The worldwide production in 1991 was estimated at about 1,785,000 t/yr (3). 

Vinyhdene chloride copolymerizes randomly with methyl acrylate and nearly so with other acrylates. Very severe composition drift occurs, however, in copolymerizations with vinyl chloride or methacrylates. Several methods have been developed to produce homogeneous copolymers regardless of the reactivity ratio (43). These methods are appHcable mainly to emulsion and suspension processes where adequate stirring can be maintained. Copolymerization rates of VDC with small amounts of a second monomer are normally lower than its rate of homopolymerization. The kinetics of the copolymerization of VDC and VC have been studied (45—48). 

O.JVI. Scott Sons. The O.M. Scott Sons Co. (Scotts) has developed a series of coated products which utilize copolymer blends of vinyHdene chloride copolymerized with methyl methacrylates, acrylonitriles, methyl acrylates, and/or vinyHdene—vinyl chloride monomers. 

A number of other copolymers with vinylidene chloride as the major component have been marketed. Prominent in the patent literature are methyl methacrylate, methyl acrylate and ethyl acrylate. 

II. B polyethylene glycol, ethylene oxide, polystyrene, diisocyanates (urethanes), polyvinylchloride, chloroprene, THF, diglycolide, dilac-tide, <5-valerolactone, substituted e-caprolactones, 4-vinyl anisole, styrene, methyl methacrylate, and vinyl acetate. In addition to these species, many copolymers have been prepared from oligomers of PCL. In particular, a variety of polyester-urethanes have been synthesized from hydroxy-terminated PCL, some of which have achieved commercial status (9). Graft copolymers with acrylic acid, acrylonitrile, and styrene have been prepared using PCL as the backbone polymer (60). 

Figure 3. Time dependence of the fraction R of unreacted aminostyrene residues during acetylation by 0.14 M acetic anhydride at 30°C. Methyl methacrylate copolymer in acetonitrile solution (0) linear poly-(methyl methacrylate-co-butyl methacrylate) swollen with acetonitrile Cd) methyl methacrylate copolymer crosslinked with 1 mole% ( ) and with 15 mole% ( ) ethylene dimethacrylate poly(methacrylate crosslinked with 3 mole% ethylene dimethacrylate containing entrapped poly(methyl acrylate-co-aminostyrene) ( ).

A number of solid acrylic resins, all known under the commercial name of Paraloid, are used in art conservation, dissolved in organic solvents, as consolidants, coatings, or in varnish formulations these resins are generally copolymers formed by two acrylic/ methacrylic monomers [82], Paraloid B-72 is the most widely used acrylic resin in conservation, and is formed by a methyl acrylate/ethyl methacrylate (MA/EMA) copolymer with molar composition 70/30. 

Uses Copolymerized with methyl acrylate, methyl methacrylate, vinyl acetate, vinyl chloride, or 1,1-dichloroethylene to produce acrylic and modacrylic fibers and high-strength fibers ABS (acrylonitrile-butadiene-styrene) and acrylonitrile-styrene copolymers nitrile rubber cyano-ethylation of cotton synthetic soil block (acrylonitrile polymerized in wood pulp) manufacture of adhesives organic synthesis grain fumigant pesticide monomer for a semi-conductive polymer that can be used similar to inorganic oxide catalysts in dehydrogenation of tert-butyl alcohol to isobutylene and water pharmaceuticals antioxidants dyes and surfactants. 

Compositionally uniform copolymers of tributyltin methacrylate (TBTM) and methyl methacrylate (MMA) are produced in a free running batch process by virtue of the monomer reactivity ratios for this combination of monomers (r (TBTM) = 0.96, r (MMA) = 1.0 at 80°C). Compositional ly homogeneous terpolymers were synthesised by keeping constant the instantaneous ratio of the three monomers in the reactor through the addition of the more reactive monomer (or monomers) at an appropriate rate. This procedure has been used by Guyot et al 6 in the preparation of butadiene-acrylonitrile emulsion copolymers and by Johnson et al (7) in the solution copolymerisation of styrene with methyl acrylate. 

The temperature optimization for the RAFT polymerization of EAA revealed an optimum reaction temperature of 70 °C. Block copolymers with a poly(methyl acrylate) (PMA), a poly(n-butyl acrylate) (PnBA), a PMMA, or a poly(A,A-dimethyl aminoethyl methacrylate) (PDMAEMA) first block and a poly(l-ethoxyethyl acrylate) (PEEA) second block were successfully synthesized in an automated synthesizer. The synthesis robot was employed for the preparation of 16 block copolymers consisting of 25 units of the first block composed of PMA (exp. 1 ), PnBA (exp. 5-8), PMMA (exp. 9-13), and PDMAEMA (exp. 13-16) and a second block of PEEA consisting of 25, 50, 75, or 100 units, respectively. The first blocks were polymerized for 3 h and a sample from each reaction was withdrawn for SEC analysis. Subsequently, EAA was added and the reactions were continued for 12 h. The molar masses and PDI values of the obtained block copolymers are shown in Fig. 15. 

Ethylene copolymers with methyl methacrylate and ethyl, butyl, and methyl acrylates are similar to EVA products but have improved thermal stability during extrusion and increased low-temperature flexibility. The commercial products generally contain 15-30% of the acrylate or methacrylate comonomer. Applications include medical packaging, disposable gloves, hose, tubing, gaskets, cable insulation, and squeeze toys. 

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