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One of the simplest repeat units is that of the addition polymer polyvinyl chloride, -[CH 2-CHCl] n-, whose repeat unit is -[CH 2-CHCl]-.In this case the repeat unit has the same atoms as the monomer vinyl chloride CH 2 =CHCl.
Polymers that are formed by free-radical mechanisms, such as polyvinyl chloride are usually atactic. [citation needed] Due to their random nature atactic polymers are usually amorphous. [citation needed] In hemi-isotactic macromolecules every other repeat unit has a random substituent. [citation needed]
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 ).
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.
A polymer which contains only a single type of repeat unit is known as a homopolymer, while a polymer containing two or more types of repeat units is known as a copolymer. [22] A terpolymer is a copolymer which contains three types of repeat units. [23] Polystyrene is composed only of styrene-based repeat units, and is classified as a homopolymer.
Polyvinyl fluoride is a thermoplastic fluoropolymer with a repeating vinyl fluoride unit, and it is structurally very similar to polyvinyl chloride. History
Vinyl polymers are subject of several structural variations, which greatly expands the range of polymers and their applications. With the exception of polyethylene, vinyl polymers can arise from head-to-tail linking of monomers, head-to-head combined with tail-to-tail, or a mixture of those two patterns. Additionally the substituted carbon center in such polymers is stereogenic (a "chiral center")
When a monomer adds to a radical chain end, there are two factors to consider regarding its stereochemistry: 1) the interaction between the terminal chain carbon and the approaching monomer molecule and 2) the configuration of the penultimate repeating unit in the polymer chain. [4] The terminal carbon atom has sp 2 hybridization and is planar.