Polymer acrylic polymer

Examples polyolefins, polydienes, vinyl polymers, acrylic polymers... 

INTEX STABILIZER 17 is an additive to a pad bath designed to give better heat and shear stability to emulsion systems in the presence of inorganic salts. It will stabilize acrylic soil release polymers, acrylic polymers, vinyl acetate polymers, styrene butadiene polymers, urethane emulsions and silicone emulsions. 

Acrylic polymer Acrylic polymer resins. See Polyacrylic acid... 

Synonyms Acrylic acid homopolymer Acrylic acid polymer Acrylic acid, polymers Acrylic acid resin Acrylic polymer Acrylic polymer resins Acrylic resin Atactic poly(acrylic acid) PAA Polyacrylate Poly (acrylic acid) 2-Propenoic acid, homopolymer Propenoic acid polymer Propenoic acid, polymers, homopolymer IMinition Polymer of acrylic acid En rirical (CjHjOj),... 

As a companion to the biguanide main-chain polymers, acrylic polymers with biguanide pendant groups were also sjmthesized (Figure 19) (polymer Cll). Polymers were synthesized by free radical polymerization, both as homopolymers and as copolymers of the biguanide monomer with acrylamide. MIC values for these polymers were substantially higher than for the monomer. The authors hypothesized that these results may be due to the fact that the polymers complex with anionic components in the culture media. As a comparison to this... 

Fig. XV-1. Plots of t/CRT vs. C for a fractionated poly(methyl acrylate) polymer at the indicated temperatures in degrees Celsius. [From A. Takahashi, A. Yoshida, and M. Kawaguchi, Macromolecules, 15, 1196 (1982) (Ref. 1). Copyright 1982, American Chemical Society.]...

In practice, synthetic polymers are sometimes divided into two classes, thermosetting and thermo-plMtic. Those polymers which in their original condition will fiow and can be moulded by heat and pressime, but which in their finished or cured state cannot be re softened or moulded are known as thermo setting (examples phenol formaldehyde or urea formaldehyde polymer). Thermoplastic polymers can be resoftened and remoulded by heat (examples ethylene polymers and polymers of acrylic esters). 

Acrylate copolymers Acrylate ester Acrylate esters Acrylate grouts Acrylate polymers Acrylates... 

Acrylic acid polymers Acrylic adhesives Acrylic anhydride Acrylic copolymer Acrylic-cotton blends Acrylic elastomers... 

Resin and Polymer Solvent. Dimethylacetamide is an exceUent solvent for synthetic and natural resins. It readily dissolves vinyl polymers, acrylates, ceUulose derivatives, styrene polymers, and linear polyesters. Because of its high polarity, DMAC has been found particularly useful as a solvent for polyacrylonitrile, its copolymers, and interpolymers. Copolymers containing at least 85% acrylonitrile dissolve ia DMAC to form solutions suitable for the production of films and yams (9). DMAC is reportedly an exceUent solvent for the copolymers of acrylonitrile and vinyl formate (10), vinylpyridine (11), or aUyl glycidyl ether (12). 

Acrylates are primarily used to prepare emulsion and solution polymers. The emulsion polymerization process provides high yields of polymers in a form suitable for a variety of appHcations. Acrylate polymer emulsions were first used as coatings for leather in the eady 1930s and have found wide utiHty as coatings, finishes, and binders for leather, textiles, and paper. Acrylate emulsions are used in the preparation of both interior and exterior paints, door poHshes, and adhesives. Solution polymers of acrylates, frequentiy with minor concentrations of other monomers, are employed in the preparation of industrial coatings. Polymers of acryHc acid can be used as superabsorbents in disposable diapers, as well as in formulation of superior, reduced-phosphate-level detergents. 

Solution Properties. Typically, if a polymer is soluble ia a solvent, it is soluble ia all proportions. As solvent evaporates from the solution, no phase separation or precipitation occurs. The solution viscosity iacreases continually until a coherent film is formed. The film is held together by molecular entanglements and secondary bonding forces. The solubiUty of the acrylate polymers is affected by the nature of the side group. Polymers that contain short side chaias are relatively polar and are soluble ia polar solvents such as ketones, esters, or ether alcohols. As the side chaia iacreases ia length the polymers are less polar and dissolve ia relatively nonpolar solvents, such as aromatic or aUphatic hydrocarbons. 

Acrylic polymers are considered to be nontoxic. In fact, the FDA allows certain acrylate polymers to be used in the packaging and handling of food. However, care must be exercised because additives or residual monomers present in various types of polymers can display toxicity. For example, some acryflc latex dispersions can be mild skin or eye irritants. This toxicity is usually ascribed to the surfactants in the latex and not to the polymer itself. 

Adhesives. Acryhc emulsion and solution polymers form the basis of a variety of adhesive types. The principal use is in pressure-sensitive adhesives, where a film of a very low T (<—20 " C) acrylic polymer or copolymer is used on the adherent side of tapes, decals, and labels. Acrylics provide a good balance of tack and bond strength with exceptional color stabiUty and resistance to aging (201,202). AcryUcs also find use in numerous types of constmction adhesive formulations and as film-to-film laminating adhesives (qv). 

Preparation, Properties and Uses of Acrylic Polymers, CM-19, Rohm and Haas Co., Philadelphia, Pa. 

A number of methods such as ultrasonics (137), radiation (138), and chemical techniques (139—141), including the use of polymer radicals, polymer ions, and organometaUic initiators, have been used to prepare acrylonitrile block copolymers (142). Block comonomers include styrene, methyl acrylate, methyl methacrylate, vinyl chloride, vinyl acetate, 4-vinylpyridine, acryUc acid, and -butyl isocyanate. 

Acrylamide—acrylic polymers are made by free-radical polymerization of monomers containing the acryHc stmcture, where R is —H or —CH and is —NH2 or a substituted amide or the alkoxy group of an ester. 

The most common VI improvers are methacrylate polymers and copolymers, acrylate polymers (see Acrylic ester polymers), olefin polymers and copolymers, and styrene—butadiene copolymers. The degree of VI improvement from these materials is a function of the molecular weight distribution of the polymer. VI improvers are used in engine oils, automatic transmission fluids, multipurpose tractor fluids, hydrautic fluids, and gear lubricants. Their use permits the formulation of products that provide satisfactory lubrication over a much wider temperature range than is possible using mineral oils alone. 

T is the glass-transition temperature at infinite molecular weight and is the number average molecular weight. The value of k for poly(methyl methacrylate) is about 2 x 10 the value for acrylate polymers is approximately the same (9). A detailed discussion on the effect of molecular weight on the properties of a polymer may be found in Reference 17. 

Acrylic Polymers. Although considerable information on the plasticization of acryUc resins is scattered throughout journal and patent hterature, the subject is compHcated by the fact that acryUc resins constitute a large family of polymers rather than a single polymeric species. An infinite variation in physical properties may be obtained through copolymerization of two or more acryUc monomers selected from the available esters of acryUc and methacryhc acid (30) (see Acrylic esterpolya rs Methacrylic acid and derivatives). 

Acrylic ESTER POLYMERS Acrylonitrile POLYMERS Cellulose esters). Engineering plastics (qv) such as acetal resins (qv), polyamides (qv), polycarbonate (qv), polyesters (qv), and poly(phenylene sulfide), and advanced materials such as Hquid crystal polymers, polysulfone, and polyetheretherketone are used in high performance appHcations they are processed at higher temperatures than their commodity counterparts (see Polymers containing sulfur). 

Catalysts. Silver and silver compounds are widely used in research and industry as catalysts for oxidation, reduction, and polymerization reactions. Silver nitrate has been reported as a catalyst for the preparation of propylene oxide (qv) from propylene (qv) (58), and silver acetate has been reported as being a suitable catalyst for the production of ethylene oxide (qv) from ethylene (qv) (59). The solubiUty of silver perchlorate in organic solvents makes it a possible catalyst for polymerization reactions, such as the production of butyl acrylate polymers in dimethylformamide (60) or the polymerization of methacrylamide (61). Similarly, the solubiUty of silver tetrafiuoroborate in organic solvents has enhanced its use in the synthesis of 3-pyrrolines by the cyclization of aHenic amines (62). 

The most commonly used scale inhibitors are low molecular weight acrylate polymers and organophosphoms compounds (phosphonates). Both classes of materials function as threshold inhibitors however, the polymeric materials are more effective dispersants. Selection of a scale control agent depends on the precipitating species and its degree of supersaturation. The most effective scale control programs use both a precipitation inhibitor and a dispersant. In some cases this can be achieved with a single component (eg, polymers used to inhibit calcium phosphate at near neutral pH). 

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