Styrenic plastics methacrylate acrylonitrile butadiene

ISO 10366-1 2002 Plastics - Methyl methacrylate-acrylonitrile-butadiene-styrene (MABS) moulding and extrusion materials - Part 1 Designation system and basis for specifications ISO 10366-2 2003 Plastics - Methyl methacrylate-acrylonitrile-butadiene-styrene (MABS) moulding and extrusion materials - Part 2 Preparation of test specimens and determination of properties... 

Terlux Clear methyl methacrylate-acrylonitrile-butadiene-styrene, MABS BASF Plastics... 

Butadiene is used primarily in the production of synthetic rubbers, including styrene-butadiene rubber (SBR), polybutadiene nibber (BR), styrene-butadiene latex (SBL), chloroprene rubber (CR) and nitrile rubber (NR). Important plastics containing butadiene as a monomeric component are shock-resistant polystyrene, a two-phase system consisting of polystyrene and polybutadiene ABS polymers consisting of acrylonitrile, butadiene and styrene and a copolymer of methyl methacrylate, butadiene and styrene (MBS), which is used as a modifier for poly(vinyl chloride). It is also used as an intermediate in the production of chloroprene, adiponitrile and other basic petrochemicals. The worldwide use pattern for butadiene in 1981 was as follows (%) SBR + SBL, 56 BR, 22 CR, 6 NR, 4 ABS, 4 hexamethylenediamine, 4 other, 4. The use pattern for butadiene in the United States in 1995 was (%) SBR, 31 BR, 24 SBL, 13 CR, 4 ABS, 5 NR, 2 adiponitrile, 12 and other, 9 (Anon., 1996b). 

This study was therefore undertaken to prepare and evaluate acrylonitrile—butadiene-styrene (ABS) and methyl methacrylate-butadiene-styrene (MBS) polymers under similar conditions to determine whether replacement of acrylonitrile by methyl methacrylate could improve color stability during ultraviolet light aging, without detracting seriously from the good mechanical and thermal-mechanical properties of conventional ABS plastics. For purposes of control, the study also included briefer evaluation of commercial ABS, MBS, and acrylonitrile-butyl acrylate-styrene plastics. 

The thermoplastic polymers we studied included the polyolefins as polyethylene and polypropylene the polyacrylates and methacrylates as poly (methyl methacrylate) styrene polymers including both clear and impact types and acrylonitrile-butadiene-styrene (ABS) plastics. Fire retardance was evaluated by the D-635 procedure as described previously (19). 

Thermoplastics are plastics which undergo a softening when heated to a particular temperature. This thermoplastic behaviour is a consequence of the absence of covalent bonds between the polymeric chains, which remain as practically independent units linked only by weak electrostatic forces (Figure 1.4(a)). Therefore, waste thermoplastics can be easily reprocessed by heating and forming into a new shape. From a commercial point of view, the most important thermoplastics are high density polyethylene (HDPE), low density polyethylene (LDPE), polypropylene (PP), polystyrene (PS), polyvinyl chloride (PVC), polyethylene tereph-thalate (PET), polyamide (PA), polymethyl methacrylate (PMMA), acrylonitrile-butadiene-styrene copolymer (ABS), and styrene-acrylonitrile copolymer (SAN). 

In spite of the great discoveries by Ziegler and Natta, most synthetic polymers are still made by free-radical reactions. Some of the important homopolymers are poly (vinyl chloride), poly (methyl methacrylate), polystyrene, and low-density polyethylene. Other important polymers made by free-radical reactions contain two or more monomers, for example, the styrene-butadiene rubbers, and the acrylonitrile-butadiene-styrene plastics. Most of these polymers are not stereoregular. A few that are represent the subject of this section. 

Plasticizers These are required to reduce the inherent brittleness of poly(alkyl-2-cyanoacrylates). This can be achieved by using non-copolymerizing plasticizers such as esters or higher alkyl cyanoacrylates, which copolymerize with the basic adhesive monomer. Toughness properties can be improved by the inclusion of rubber toughening materials such as ABS (acrylonitrile-butadiene-styrene) or MBS (methacrylate-butadiene-styrene) copolymers. Whichever approach is adopted, toughness is only achieved at the expense of reduced cure speed. 

Develop a heat-transfer analysis for radiant heating of a coextruded sheet of plastic material (example thickness of 0.5 cm of polymethyl methacrylate and 0.75 cm of acrylonitrile-butadiene-styrene, or ABS). Assume that the heating flux to each side is the same. 

Plastics materials and resins), for example, acrylics, acrylonitrile-butadiene-styrene, alkyds carbohydrate, casein, and cellulose acetate plastics cellulose nitrates elastomers epoxy, ethylene-vinyl acetate, ion exchange, methyl cellulose, methyl methacrylate, nitrocellulose, nylon, polyacrylonitrile, polyamide, polycarbonate, polyester, polyethylene, polyethylene terephthalate, polyurethane, polyvinyl alcohol, polyvinyl chloride, silicone, urea, resins thermoplastics, thermosets... 

Acrylonitrile resembles VC, a carcinogen, in structure. It is a flammable, explosive liquid (b.p. 77 C, V.P. 80 mm at 20°C). AN is a component of acrylic and modacrylic fibers produced by copolymerization with other monomers, e.g., with methyl acrylate, Me-methacrylate, vinyl acetate, VC and VDC. Other major uses of AN include copolymerizations with butadiene and styrene to produce ABS polymers, and with styrene to yield SAN resins which are used in the manufacture of plastics. Nitrile elastomers and latexes are also made with AN, as are a number of other chemicals, e.g. acrylamide and adiponitrile. Acrylonitrile is also used as a fumigant. 

Copolymers of styrene include a large group of random, graft, and block copolymers. Those with a high proportion of acrylonitrile used in barrier films as well as others such as methacrylic-butadiene-styrene copolymer (MBS) plastic is used as modifiers in PVC, SAN, ABS, ASA, etc. The styrene-acrylonitrile copolymer (SAN) is the most important when considering volume and number of applications. 

Polyacrylonitrile is most often encountered as a fiber. It is also found in acrylonitrile-containing plastics copolymerized with styrene, butadiene, or methyl methacrylate. All such polymers contain nitrogen. 

Poly(vinyl chloride) (PVC) homopolymer is a stiff, rather brittle plastic with a glass temperature of about 80°C. While somewhat more ductile than polystyrene homopolymer, it is still important to blend PVC with elastomer systems to improve toughness. For example, methyl methacrylate-butadiene-styrene (MBS) elastomers can impart impact resistance and also optical clarity (see Section 3.3). ABS resins (see Section 3.1.2) are also frequently employed for this purpose. Another of the more important mechanical blends of elastomeric with plastic resins is based on poly(vinyl chloride) as the plastic component, and random copolymers of butadiene and acrylonitrile (AN) as the elastomer (Matsuo, 1968). On incorporation of this elastomeric phase, PVC, which is ordinarily a stiff, brittle plastic, can be toughened greatly. A nonpolar homopolymer rubber such as polybutadiene (PB) is incompatible with the polar PVC. Indeed, electron microscopy shows... 

---