Vinyl Ester Monomer

Acetic acid ethenyl ester.

Vinyl ester monomer. Vinyl acetate is the acetate ester of vinyl alcohol. Veova eh monomer is the vinyl ester of 2 ethylhexanoic acid a more linear acid and therefore has a significantly lower tg of 36 c. Veova monomer products include. In chemistry vinyl or ethenyl abbreviated as vi is the functional group with the formula c h ch 2 it is the ethylene iupac ethene molecule h 2 c ch 2 with one fewer hydrogen atom.

In vinyl ester polymerization the very different reactivities of the growing radicals high and the monomer low result in a high level of chain transfer reactions and main chain irregularities which make the production of uniform polymers rather difficult. An industrially important example is vinyl chloride precursor to pvc a plastic. Veova 10 monomer is the vinyl ester of neodecanoic acid 10 carbon atoms and has a homopolymer tg of 3 c making it a flexibilizing monomer. They are increasingly used in radiation curing systems because of a lower toxicity profile than the commonly used acrylic monomers.

Since vinyl alcohol is highly unstable with respect to acetaldehyde the preparation of vinyl acetate is more complex than the synthesis of other acetate esters. This structure is also available as a 2d mol file or as a computed 3d sd file the 3d structure may be viewed using java or javascript. Vinyl ester resins are the binary resin systems containing a dimethacrylate monomer from which the cured material gains most of its properties and a reactive monomer such as styrene which acts as a reactive diluent and also takes part in the cross linking reaction. The major industrial route involves the reaction of ethylene and acetic acid with oxygen in the presence of a palladium catalyst.

Acetic acid ethylene ether. Veova 10 vinyl ester homopolymer. The name is also used for any compound containing that group namely r ch ch 2 where r is any other group of atoms. Veova 9 vinyl ester homopolymer tg 70 c.

Vinyl acetate is not as hydrolytically stable in polymers as are the structurally similar acrylic esters. Vinyl esters undergo homopolymerization via a radical mechanism. Vinyl alcohol containing polymers are prepared by hydrolysis of the corresponding vinyl acetate polymers. The most widely used member of the category is vinyl acetate.

Advances in fire retardant materials 2008. Vinyl ethers undergo homopolymerization via a cationic mechanism. Vinile acetato di vinylacetaat dutch vinylacetat german vinyle acetate de octan winylu polish acetic acid vinyl ester. Ethanoic acid ethenyl ester.

Vinyl ethers undergo radical initiated copolymerization in the presence of specific monomers such as maleates fumarates and acrylics.