Ethyl copolymers with methyl acrylate

The polarity of any species is independent of whether it is in monomer or radical form for the free radical is a neutral entity. Thus assuming that the above types of polarization are also possible with radicals, one can understand that a chain end at which there happens to be a structural unit with an electron-withdrawing substituent, prefers a monomer with an electron-donating substituent and vice versa. Such consideration of polarity explains that, for example, acrylonitrile forms statistical copolymers with methyl acrylate (rir2 = 1.26), while copolymerization of acrylonitrile with ethyl vinyl ethers leads to alternating structures (r r2 == 0.04). 

A number of higher poly(vinyl ether)s, in particular the ethyl and butyl polymers, have found use as adhesives. When antioxidants are incorporated, pressure-sensitive adhesive tapes from poly(vinyl ethyl ether) are said to have twice the shelf life of similar tapes from natural rubber. Copolymers of vinyl isobutyl ether with methyl acrylate and ethyl acrylate (Acronal series) and with vinyl chloride have been commercially marketed. The first two products have been used as adhesives and impregnating agents for textile, paper and leather whilst the latter (Vinoflex MP 400) has found use in surface coatings. 

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. 

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. 

Macroradicals obtained by the copolymerization of equimolar quantities of styrene and maleic anhydride in benzene or in cumene were also used as initiators to produce block copolymers with methyl methacrylate, ethyl methacrylate, and methyl acrylate. The yields of these block copolymers were less than those obtained with styrene, but as much as 38% of methyl methacrylate present in the benzene solution added to the macroradical to produce a block copolymer. The amount of ethyl methacrylate and methyl acrylate that was abstracted from the solution to form block copolymers was 35 and 20%. 

Another approach to improving the properties of starch-filled polyolefin materials involves the use of ethylene-acrylate copolymers in blends with PE.45 Addition of copolymers of ethylene with methyl acrylate, ethyl acrylate or butyl acrylate were shown to improve the properties of PE films, allowing for higher starch contents. Coextrusion of starch-containing films with outer layers incorporating oxidative pro-degradants has also been utilized 46 The inner layer can contain up to 40% starch the... 

Quite frequently, copolymerization is used to optimize the properties of polyacrylates. For example, copolymers of ethyl acrylate with methyl acrylate provide the required hardness and strength, while small amounts of comonomers with hydroxyl, carboxyl, amine, and amide functionalities are used to produce high-quality latex paints for wood, wallboard, and masonry in homes. These functionalities provide the adhesion and thermosetting capabilities required in these applications. Monomers with the desired functional groups most often used in copolymerization with acrylates are shown in Table 15.8. 

Emulsion Polymerization. Emulsion polymerization is the most important industrial method for the preparation of acryhc polymers. The principal markets for aqueous dispersion polymers made by emulsion polymerization of acryhc esters are the paint, paper, adhesives, textile, floor pohsh, and leather industries, where they are used principally as coatings or binders. Copolymers of either ethyl acrylate or butyl acrylate with methyl methacrylate are most common. 

AH-acryHc (100%) latex emulsions are commonly recognized as the most durable paints for exterior use. Exterior grades are usuaHy copolymers of methyl methacrylate with butyl acrylate or 2-ethyIhexyl acrylate (see Acrylic ester polymers). Interior grades are based on methyl methacrylate copolymerized with butyl acrylate or ethyl acrylate. AcryHc latex emulsions are not commonly used in interior flat paints because these paints typicaHy do not require the kind of performance characteristics that acryHcs offer. However, for interior semigloss or gloss paints, aH-acryHc polymers and acryHc copolymers are used almost exclusively due to their exceUent gloss potential, adhesion characteristics, as weU as block and print resistance. 

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. 

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. 

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. 

Figure 41. A plot of sensitivity to Mo (5.4k) x-ray radiation and 20 kV electron beam radiation for several resists. EPB is epoxidized polybutadiene, P(GMA-EA) is a copolymer of glycidyl methacrylate and ethyl acrylate (COP), PGMA is poly (glycidyl methacrylate), PBS is poly (butene-1 -sulfone), FBM-1 is poly (2,2,3,3-tetrafluoropropyl methacrylate), P(MMA-MA) is a copolymer of methyl methacrylate and methacrylic acid, PMMA is poly (methyl methacrylate). (Reproduced with permission from Ref. 56J...

The most widely used acrylic plastics are PMMA (Lucite) or copolymers of methyl methacrylate with small amounts (2 to 18%) of methyl or ethyl acrylate (Plexiglas). These commercial products, which are available as sheets and as molding powders, have a specific gravity of about 1.2, a heat deflection temperature of about 95 C, a refractive index of about 1.5, and a water absorption of 0.2%. PMMA is more resistant to impact than PS or glass, but its scratch resistance is inferior to that of glass,... 

Copolymers of acrylonitrile and methyl acrylate and terpolymers of acrylonitrile, styrene, and methyl methacrylate are used as bamer polymers. Acrylonitrile copolymers and multipolymers containing butyl acrylate, ethyl aciylate, 2-ethylhexyl acrylate, hydroxyethyl acrylate, methyl methaciylate. vinyl acetate, vinyl ethers, and vinylidene chlonde are also used in bamer films, laminates, and coatings. Environmentally degradable polymers useful in packaging are prepared from polymerization of acrylonitrile with styrene and methyl vinyl ketone. 

The structure of copolymers obtained by ATRP copolymerization of 5,6-benzo-2-methylene-l,3-dioxepane (BMDO) with H-butyl acrylate ( BA) using ethyl 2-bromoisobutyrate and iV,iV,iV, iV ,iV -pentamethyldiethylenetri-amine/copper(l) bromide, as the initiator and catalyst, respectively, was studied by ID and 2D NMR techniques, which revealed a quantitative ring opening of BMDO in the copolymerization <2005PLM11698>. For a similar study of copolymers of BMDO and styrene, see <2003MM6152>, and with methyl methacrylate, <2003MM2397>. 

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