Vinyl Ester Monomer

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.

Vinyl ester monomer.

They are increasingly used in radiation curing systems because of a lower toxicity profile than the commonly used acrylic monomers. Vinile acetato di vinylacetaat dutch vinylacetat german vinyle acetate de octan winylu polish acetic acid vinyl ester. Vinyl acetate is the acetate ester of vinyl alcohol. 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. Acetic acid vinyl ester. Vinyl alcohol containing polymers are prepared by hydrolysis of the corresponding vinyl acetate polymers. 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.

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 eh monomer is the vinyl ester of 2 ethylhexanoic acid a more linear acid and therefore has a significantly lower tg of 36 c. 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. Vinyl acetate is not as hydrolytically stable in polymers as are the structurally similar acrylic esters.

Veova 9 vinyl ester homopolymer tg 70 c. The most widely used member of the category is vinyl acetate. Emulsion polymers based on veova vinyl ester show clear improvement in scrub resistance and can be used for high quality low voc interior paints exterior paints industrial coatings as well as redispersible powders for dry mix mortars. Vinyl ethers undergo radical initiated copolymerization in the presence of specific monomers such as maleates fumarates and acrylics.

Acetic acid ethenyl ester. Vinyl esters undergo homopolymerization via a radical mechanism. Vinyl ethers undergo homopolymerization via a cationic mechanism. 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.

The major industrial route involves the reaction of ethylene and acetic acid with oxygen in the presence of a palladium catalyst. Ethanoic acid ethenyl ester. Veova 10 vinyl ester homopolymer. Advances in fire retardant materials 2008.

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