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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")
The polymer is formed by the condensation reaction of the two monomers terephthalic acid (HOOC-C 6 H 4-COOH) and ethylene glycol (HO-CH 2-CH 2-OH), or their chemical derivatives. The condensation involves loss of water, as an H is lost from each HO- group in the glycol, and an OH from each HOOC- group in the acid.
In a fire, PVC can form hydrogen chloride fumes; the chlorine serves to scavenge free radicals, making PVC-coated wires fire retardant. While hydrogen chloride fumes can also pose a health hazard in their own right, it dissolves in moisture and breaks down onto surfaces, particularly in areas where the air is cool enough to breathe, so would ...
It is the ethylene (IUPAC name: ethene) molecule (H 2 C=CH 2) with one fewer hydrogen atom. The name is also used for any compound containing that group, namely R−CH=CH 2 where R is any other group of atoms. An industrially important example is vinyl chloride, precursor to PVC, [3] a plastic commonly known as vinyl. Chessboard made from ...
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 (/ ˈ p ɒ l ɪ m ər / [4] [5]) is a substance or material that consists of very large molecules, or macromolecules, that are constituted by many repeating subunits derived from one or more species of monomers. [6]
Propylene, also known as propene, is an unsaturated organic compound with the chemical formula CH 3 CH=CH 2. It has one double bond , and is the second simplest member of the alkene class of hydrocarbons .
Due to side reactions, not all radicals formed by the dissociation of initiator molecules actually add monomers to form polymer chains. The efficiency factor f is defined as the fraction of the original initiator which contributes to the polymerization reaction. The maximal value of f is 1, but typical values range from 0.3 to 0.8. [7]