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Acrylonitrile is an organic compound with the formula CH 2 CHCN and the structure H 2 C=CH−C≡N. It is a colorless, volatile liquid. It has a pungent odor of garlic or onions. [ 4 ]
Acrylonitrile butadiene styrene (ABS) (chemical formula (C 8 H 8) x · (C 4 H 6) y · (C 3 H 3 N) z) is a common thermoplastic polymer. Its glass transition temperature is approximately 105 °C (221 °F). [4] ABS is amorphous and therefore has no true melting point. ABS is a terpolymer made by polymerizing styrene and acrylonitrile in the ...
Acrylonitrile is commonly employed as a comonomer with styrene, e.g. acrylonitrile, styrene and acrylate plastics. Labelling of items of clothing with acrylic (see acrylic fiber) means the polymer consists of at least 85% acrylonitrile as the monomer. A typical comonomer is vinyl acetate, which can be solution-spun readily to obtain fibers that ...
Acrylonitrile styrene acrylate (ASA), also called acrylic styrene acrylonitrile, is an amorphous thermoplastic developed as an alternative to acrylonitrile butadiene styrene (ABS), that has improved weather resistance. It is an acrylate rubber-modified styrene acrylonitrile copolymer.
An alternative version of NBR is carboxylated nitrile butadiene rubber (XNBR). XNBR is a terpolymer of butadiene, acrylonitrile, and acrylic acid. [11] The presence of the acrylic acid introduces carboxylic acid groups (RCO 2 H). These groups allow crosslinking through the addition of zinc (Zn 2+) additives. The carboxyl groups are present at ...
Styrene acrylonitrile resin (SAN) is a copolymer plastic consisting of styrene and acrylonitrile. It is widely used in place of polystyrene owing to its greater thermal resistance. The chains of between 70 and 80% by weight styrene and 20 to 30% acrylonitrile. [ 1 ]
Polybutadiene acrylonitrile (PBAN) [1] copolymer, also noted as polybutadiene—acrylic acid—acrylonitrile terpolymer [2] is a copolymer compound used most frequently as a rocket propellant fuel mixed with ammonium perchlorate oxidizer. [3] It was the binder formulation widely used on the 1960s–1970s big boosters (e.g., Titan III and Space ...
Acetonitrile has only modest toxicity in small doses. [ 11 ] [ 19 ] It can be metabolised to produce hydrogen cyanide , which is the source of the observed toxic effects. [ 9 ] [ 20 ] [ 21 ] Generally the onset of toxic effects is delayed, due to the time required for the body to metabolize acetonitrile to cyanide (generally about 2–12 hours).