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Vinyl acetate is the acetate ester of vinyl alcohol. 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. The major industrial route involves the reaction of ethylene and acetic acid with oxygen in the presence of a palladium catalyst. [6]
Recycling codes on products. Recycling codes are used to identify the materials out of which the item is made, to facilitate easier recycling process.The presence on an item of a recycling code, a chasing arrows logo, or a resin code, is not an automatic indicator that a material is recyclable; it is an explanation of what the item is made of.
Vinyl polymers are the most common type of plastic. Important examples can be distinguished by the R group in the monomer H 2 C=CHR: Polyethylene R = H; polypropylene from propylene, R = CH 3; Polystyrene is made from styrene, R = C 6 H 5; Polyvinyl chloride (PVC) is made from vinyl chloride, R= Cl; Polyvinyl acetate (PVAc) is made from vinyl ...
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Polyvinyl acetate was discovered in Germany in 1912 by Fritz Klatte. [3] The monomer, vinyl acetate, was first produced on an industrial scale by the addition of acetic acid to acetylene with a mercury(I) salt, [4] but it is now primarily made by palladium-catalyzed oxidative addition of acetic acid to ethylene.
Vinyl neodecanoate (trade name VeoVa 10) is a vinylic monomer that is virtually always used in combination with other monomers to create latices or emulsion polymers. [3] The trade name is an acronym of Vinyl ester of Versatic Acid with the number 10 meaning 10 carbons in the molecule. It has a medium to low glass transition temperature of -3 °C.
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