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Acrylonitrile is produced by catalytic ammoxidation of propylene, also known as the SOHIO process. In 2002, world production capacity was estimated at 5 million tonnes per year, [5] [8] rising to about 6 million tonnes by 2017. [9] Acetonitrile and hydrogen cyanide are significant byproducts that are recovered for sale. [5]
PAN is soluble in polar solvents, such as dimethylformamide, dimethylacetamide, ethylene and propylene carbonates, and in aqueous solutions of sodium thiocyanate, zinc chloride or nitric acid. [13] Solubility parameters: 26.09 MPa 1/2 (25 °C) are 25.6 to 31.5 J 1/2 cm −3/2. Dielectric constants: 5.5 (1 kHz, 25 °C), 4.2 (1 MHz, 25 °C).Can ...
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.
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 ...
Allyl chloride is the organic compound with the formula C H 2 =CHCH 2 Cl. This colorless liquid is insoluble in water but soluble in common organic solvents. It is mainly converted to epichlorohydrin, used in the production of plastics. It is a chlorinated derivative of propylene. It is an alkylating agent, which makes it both useful and ...
Structure of the allyl group. In organic chemistry, an allyl group is a substituent with the structural formula −CH 2 −HC=CH 2.It consists of a methylene bridge (−CH 2 −) attached to a vinyl group (−CH=CH 2).
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")
Propene is also used for the production of chemicals such as propylene oxide, acrylonitrile, cumene, butyraldehyde, and acrylic acid. In the year 2013 about 85 million tonnes of propylene were processed worldwide. [17] Propylene and benzene are converted to acetone and phenol via the cumene process. Overview of the cumene process