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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.
Not all monomers are susceptible to all types of initiators. Radical initiation works best on the carbon–carbon double bond of vinyl monomers and the carbon–oxygen double bond in aldehydes and ketones. [1] Initiation has two steps. In the first step, one or two radicals are created from the initiating molecules. In the second step, radicals ...
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.
In the early 1970s, the carcinogenicity of vinyl chloride (usually called vinyl chloride monomer or VCM) was linked to cancers in workers in the polyvinyl chloride industry. Specifically workers in polymerization section of a B.F. Goodrich plant near Louisville, Kentucky , were diagnosed with liver angiosarcoma also known as hemangiosarcoma , a ...
In contrast step-growth polymerization involves only one type of step, and macromolecules can grow by reaction steps between any two molecular species: two monomers, a monomer and a growing chain, or two growing chains. [17] In step growth, the monomers will initially form dimers, trimers, etc. which later react to form long chain polymers.
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")
Usage of monomer in the reaction: Rapid loss of monomer early in the reaction: Some monomer remains even at long reaction times Reaction steps: Similar steps repeated throughout reaction process: Different steps operate at different stages of mechanism (i.e. initiation, propagation, termination, and chain transfer) Average molecular weight
Some reactive olefin monomers are shown below in order of decreasing reactivity, with heteroatom groups being more reactive than alkyl or aryl groups. Note, however, that the reactivity of the carbenium ion formed is the opposite of the monomer reactivity.