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Polymers polyvinyl acetate

Vinyl Acetate—Ethylene Copolymers. In these random copolymers, the ratio of ethylene to vinyl acetate (EVA) is varied from 30—60%. As the vinyl acetate content increases, the oil and heat resistance increases. With higher ethylene content the physical strength, tensile, and tear increases. The polymers are cured with peroxide. The main properties of these elastomers include heat resistance, moderate oil and solvent resistance, low compression set, good weather resistance, high damping, excellent ozone resistance, and they can be easily colored (see Vinyl polymers, polyvinyl acetate)). [Pg.234]

Vinyl acetate was first described in a German patent awarded to Fritz Klatte and assigned to Chemishe Fabriken Grieshiem-EIectron in 1912. It was identified as a minor by-product of the reaction of acetic acid and acetylene to produce ethylidene diacetate. By 1925, commercial interest in vinyl acetate monomer and the polymer, polyvinyl acetate, developed and processes for their production on an industrial scale were devised. The first commercial process for vinyl acetate monomer involved the addition of acetic acid to acetylene in the vapor phase using a zinc acetate catalyst supported on activated carbon. This process was developed by Wacker Chemie in the early 1930s and dominated the production of vinyl acetate until the 1960s when an ethylene-based process was commercialized which supplanted the earlier acetylene technology [24]. [Pg.181]

CDs are equably dispersed in polymer. A kind of soluble polymers (polyvinyl acetate, PAM) is chosen and dissolved in solvents (acetone, ethyl acetate). Then CD is added and scattered in the solvents. Finally, the solvent is evaporated and the CDP blend is prepared. It is the gentlest CD immobilization method, as it is not a chemical reaction, and is widely used as the operation is simple. For example, the polymer blend of CD/polyacrylamide can be used as filling materials of capillary chromatographic column. Its separation efficiency is as high as 10,000 layer/15 cm. If spices or fungicide are added to CD before blending with polyethylene, the blend products can be used as flavor enhancer or antibacterial packaging material. [Pg.174]

The use of synthetic adhesives in the past twenty-five years (1) has grown/ particularly the use of eight classes of polymers polyvinyl acetate/ polyolefins/ styrenic block copolymerS/ acrylicS/ cyanoacrylates/ anaerobicS/ polyurethanes/ and epoxy resins. Some of these polymers are Still in high demand as specialty adhesives (2). During the last several yearS/ however / other polymers have been added to this list/ e.g. / polyamides/ polyimideS/ and polyesters. Today/ synthetic adhesives account for 75% of the adhesives produced and 85% of the sales/ while the market share of natural products has steadily declined. [Pg.6]

Breuer and Robb (1972) studied the effect of polymer hydrophobicity on the interaction of polymer with surfactant. SDS was used as the anionic surfactant along with several different polymers polyvinyl acetate (PVAc), polyvinyl alcohol (PVA), polypropylene oxide (PPO), PEO, and methylcellulose (MeC). [Pg.663]

Today plasticisers are used in a variety of polymers such as polyvinyl acetate, acrylic polymers, cellulose acetate and, most important of all, poly(vinyl chloride). [Pg.131]

Lucie, S., Kovacevic, V., Packham, D.E., Bogner, A., Gerzina, A., Stearate-modified calcium carbonate fillers and their effect on the properties of polyvinyl acetate, composites. Proc. 2nd Int. Symp. Polymer Surface Modification Relevance to Adhesion, Newark, NJ, 24-26 May, 1999. [Pg.347]

Synthetic resins form the heart of the paint industry. The tw o main types of synthetic resins are condensation polymers and addition polymers. Condensation polymers, formed by condensation of like or unlike molecules into a new, more complex compound, include polyesters, phenolics.. iniino resins, polyurethane, and epoxies. Addition polymers include polyvinyl acetate, polyvinyl chloride, and the acrylates,... [Pg.285]

Heitz et al. (33) also described the preparation of polyvinyl acetate cross-linked with butanediol divinyl ether. The polymer is the base of the Merckogel series of size exclusion chromatography packings, and its hydrolyzed derivative, polyvinyl alcohol, is marketed as Fractogel and Toyopearls. [Pg.9]

Polyvinyl acetate (PVA), acrylic and other polymer dispersions have been widely used as anti-dust treatments for concrete floors for many years. In general, the polymer dispersions have been similar to those used in the manufacture of emulsion paints, and until recently have tended to be based on dispersions of relatively large polymer particles (particle size 0.15-0.25 x 10 m). Dispersions are now becoming available which offer superior performance as floor sealers. The chemical and water resistance of the various polymer dispersions which have been used in the past vary considerably from the PVA types, which are rapidly softened and eventually washed out by water, to acrylic and SBR types which exhibit excellent resistance to a wide range of chemicals. Water-based sealers are gaining wider acceptance because of... [Pg.102]

A bond coat of a polymer latex (also called polymer emulsions or dispersions) such as styrene butadiene (SBR), polyvinyl acetate (PVA) acrylics or modified acrylics. These are applied to the prepared concrete as... [Pg.104]

Organic solvents are most commonly used, and encapsulating polymers include ethylcellu-lose, NC, polvvinylidene chloride, polystyrene, polycarbonate, polymethylmethacrylate, polyvinyl acetate and others. Inter facial polymerization produces a polymer such as nylon at the interface between layered solns of two precursor materials such as (in the case of a nylon) a diamine and a diacid (Refs 3 11). If the particle or drop-... [Pg.142]

In particular, blends of PVDF with a series of different polymers (polymethylmethacrylate [100-102], polyethylmethacrylate [101], polyvinyl acetate [101]), for suitable compositions, if quenched from the melt and then annealed above the glass transition temperature, yield the piezoelectric [3 form, rather than the normally obtained a form. The change in the location of the glass transition temperature due to the blending, which would produce changes in the nucleation rates, has been suggested as responsible for this behavior. A second factor which was identified as controlling this behavior is the increase of local /rans-planar conformations in the mixed amorphous phase, due to specific interactions between the polymers [102]. [Pg.206]

This molecule is a copolymer with polymethyl methacrylate (PMMA) in acrylic latex paints, where the hydrophobic PMMA is surrounded by hydrophilic polyvinyl acetate molecules. Such a suspension of a hydrophobic polymer wrapped in a hydrophilic polymer is called a latex. [Pg.232]

The combined results of kinetic studies on condensation polymerization reactions and on the degradation of various polymers by reactions which bring about chain scission demonstrate quite clearly that the chemical reactivity of a functional group does not ordinarily depend on the size of the molecule to which it is attached. Exceptions occur only when the chain is so short as to allow the specific effect of one end group on the reactivity of the other to be appreciable. Evidence from a third type of polymer reaction, namely, that in which the lateral substituents of the polymer chain undergo reaction without alteration in the degree of polymerization, also support this conclusion. The velocity of saponification of polyvinyl acetate, for example, is very nearly the same as that for ethyl acetate under the same conditions. ... [Pg.102]

The method outlined above for characterizing branched polymers will hereafter be referred to as the molecular weight and branching distribution (MWBD) method. In the following sections, its application to the long chain branching in polyvinyl acetate and high pressure low density polyethylene will be demonstrated. [Pg.136]

In order to estimate the branching factor e for polyvinyl acetate we have analyzed the SEC data obtained on sample PVAc-E4 using the MWBD method with various e values. This sample was synthesized under kinetically controlled conditions (isothermal, T = 60°C, [AIBN] = 10"5 g-mole/1, conversion level of 48.5 percent). The SEC measurements were made at 25°C in tetrahydro-furan. The Mark-Houwink coefficients used for linear polyvinyl acetate are those suggested by Graessley (21), namely K = 5.1 x 10"5 dl/gm and a = 0.791. The whole polymer M, Mj, and B j values obtained are listed in Table II. [Pg.137]

The determination of adsorption isotherms at liquid-solid interfaces involves a mass balance on the amount of polymer added to the dispersion, which requires the separation of the liquid phase from the particle phase. Centrifugation is often used for this separation, under the assumption that the adsorption-desorption equilibrium does not change during this process. Serum replacement (6) allows the separation of the liquid phase without assumptions as to the configuration of the adsorbed polymer molecules. This method has been used to determine the adsorption isotherms of anionic and nonionic emulsifiers on various types of latex particles (7,8). This paper describes the adsorption of fully and partially hydrolyzed PVA on different-size PS latex particles. PS latex was chosen over polyvinyl acetate (PVAc) latex because of its well-characterized surface PVAc latexes will be studied later. [Pg.78]

This is just the first example of how the ADMET reaction can be used to model branching behavior and precisely control the structure in olefin-based polymer backbones. Other polymers under study include polyalcohols, polyvinyl acetates, and ethylene-styrene copolymers. The ultimate goal of this research is to be able to define, or even predict, crystallization limits and behavior for many polymers, some of which have not yet been prepared in a crystallized form. [Pg.204]

Wet spinning. This technique is characterized by spinning a filtered viscous polymer mass, dissolved in a suitable solvent, into contact with a precipitation or coagulation bath. Polyacrylonitrile, polyvinyl acetate, cellulose acetate, and other materials are processed by this method. Thermal requirements for pigments are less stringent than for melt spinning but pigments are expected to be fast to the solvents and chemicals used. [Pg.177]

When vinyl flouride is polymerized, a certain percentage of the flourine atoms are found on adjacent carbon atoms. When polyvinyl alcohol made by hydrolyzing polyvinyl acetate was treated with periodic acid by Flory, he found that the molecular weight was greatly reduced, indicating that there were 1,2-glycol units in the chain. But most of the polymers were regular head-to-tail polymers. [Pg.58]

These polymers are produced by a more or less complete hydrolysis of polyvinyl acetate. [Pg.336]

Vinyl chloride polymers and copolymers are often referred to as vinyl resins. PVC is the most important member of the vinyl resin family, which includes polyvinyl acetate (PVAC), polyvinyl alcohol (PVA), polyvinylidene chloride (PVdC) and polyvinyl acetal. Almost always the term PVC includes polymers of VCM as well as copolymers that are mostly VCM. [Pg.348]

The effect of structural regularity on properties of polymers may be illustrated by the hydrolytic products of polyvinyl acetate (PVAc). PVAc is insoluble in water, but because of the presence of polar hydroxyl groups, partially hydrolyzed PVAc is soluble in water. [Pg.27]

The most widely used polyvinyl acetal is polyvinyl butyrai (PVB). This transparent amorphous plastic is used as a plasticized polymer in the inner lining of safety windshield glass (Saflex). Because of the presence of hydroxyl groups, the commercial product, which is produced from 75% hydrolyzed PVAc, has a Tg of about 49 C and has excellent adhesion to glass. [Pg.161]

The principal synthetic polymers used as coatings are alkyd resins, styrene copolymers, polyvinyl acetate (PVAc), urea, melamine, phenolic and epoxy... [Pg.189]

When tested in other polymers, maleimides did not affect the rate of cross-linking in polydimethylsiloxane, polyisobutylene, and polyvinylchloride. In polyethylene, the addition of 5 wt.% of m-phenylene dimaleimide increased the G(X) from 1.8 to 7.2. In the polyvinylacetate the effect was even more pronounced the dose for gelation was reduced by about a factor of 50. Contrary to the cross-link enhancing effect found for m-phenylene dimaleimide, cross-linking was retarded in polyvinyl acetate by the addition of monomaleimides. When analyzing the mechanism of the reaction it was concluded that monomaleimides are not expected to affect cross-linking in saturated polymers. ... [Pg.92]

Originality Star polymers containing polyvinyl acetate and alcohols have... [Pg.76]


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