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In polymer chemistry, vinyl polymers are a group of polymers derived from substituted vinyl (H 2 C=CHR) monomers. Their backbone is an extended alkane chain [−CH 2 −CHR−] . [ 1 ] In popular usage, "vinyl" refers only to polyvinyl chloride (PVC).
Vinyl chloride is an organochloride with the formula H 2 C=CHCl. It is also called vinyl chloride monomer (VCM) or chloroethene. It is an important industrial chemical chiefly used to produce the polymer polyvinyl chloride (PVC). Vinyl chloride is a colourless flammable gas that has a sweet odor and is carcinogenic.
Polyvinyl chloride is formed in flat sheets in a variety of thicknesses and colors. As flat sheets, PVC is often expanded to create voids in the interior of the material, providing additional thickness without additional weight and minimal extra cost (see closed-cell PVC foamboard). Sheets are cut using saws and rotary cutting equipment.
An industrially important example is vinyl chloride, precursor to PVC, [3] a plastic commonly known as vinyl. Chessboard made from polyvinyl chloride. Vinyl is one of the alkenyl functional groups. On a carbon skeleton, sp 2-hybridized carbons or positions are often called vinylic. Allyls, acrylates and styrenics contain vinyl groups. (A ...
The term vinyl is often used to describe any alkenyl group. For this reason, alkenyl halides with the formula RCH=CHX are sometimes called vinyl halides. From the perspective of applications, the dominant member of this class of compounds is vinyl chloride, which is produced on the scale of millions of tons per year as a precursor to polyvinyl ...
Category: Vinyl polymers. ... This category describes polymers based on the vinyl group ... Polyvinyl chloride acetate; Polyvinyl fluoride;
The gas is used to make the polyvinyl chloride hard plastic resin in plastic products. ... Vinyl chloride is dozens of times less toxic per molecule than the U.S.-banned insecticide DDT but more ...
This mode of reactivity is analogous to the way vinyl acetate and vinyl chloride can be polymerized to form polyvinyl acetate and polyvinyl chloride, respectively. Methyl vinyl ether also participates in [4+2] cycloaddition reactions. [5] Its reaction with acrolein is the first step in the commercial synthesis of glutaraldehyde. The alkene can ...