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Acrylate-styrene-acrylonitrile, mechanical properties

Acrylonitrile—Butadiene—Styrene. ABS is an important commercial polymer, with numerous apphcations. In the late 1950s, ABS was produced by emulsion grafting of styrene-acrylonitrile copolymers onto polybutadiene latex particles. This method continues to be the basis for a considerable volume of ABS manufacture. More recently, ABS has also been produced by continuous mass and mass-suspension processes (237). The various products may be mechanically blended for optimizing properties and cost. Brittle SAN, toughened by SAN-grafted ethylene—propylene and acrylate mbbets, is used in outdoor apphcations. Flame retardancy of ABS is improved by chlorinated PE and other flame-retarding additives (237). [Pg.419]

Copolymers of acrylonitrile [107-13-1] are used in extmsion and molding appHcations. Commercially important comonomers for barrier appHcations include styrene and methyl acrylate. As the comonomer content is increased, the permeabiUties increase as shown in Figure 3. These copolymers are not moisture-sensitive. Table 7 contains descriptions of three high nitrile barrier polymers. Barex and Cycopac resins are mbber-modified to improve the mechanical properties. [Pg.490]

Several flexible polymers, such as natural rubber (NR) synthetic rubber (SR) polyalkyl acrylates copolymers of acrylonitrile, butadiene, and styrene, (ABS) and polyvinyl alkyl ethers, have been used to improve the impact resistance of PS and PVC. PS and copolymers of ethylene and propylene have been used to increase the ductility of polyphenylene oxide (PPO) and nylon 66, respectively. The mechanical properties of several other engineering plastics have been improved by blending them with thermoplastics. [Pg.131]

By chemical agents, indirect grafting on Nylon in liquid phase is frequently referred to in the bibliography. The most common reagent is air (144) or ozone, under controlled conditions, in order to avoid deterioration on the mechanical properties of the fiber, which is then immersed in the monomer. Hence, styrene (145-149), vinylidene chloride (146), vinyl acetate (146), acrylic and methacrylic acids (149), methyl methacrylate (146), acrylonitrile (146,148,149), 2-methyl-5-vinylpyridine (149) were successfully employed as grafting comonomers. [Pg.104]

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. [Pg.242]

This latex is then processed to isolate the ABS resin, ABS thermoplastic combines good mechanical properties and heat resistance. It is used in many household appliances, automotive parts, furniture, etc. Another similar terpolymer is acrylonitrile-styrene-acrylate (ASA). It is used in automobile industry, in house construction, household appliances, etc. [Pg.247]

MABS is similar to ABS except for the addition of an additional monomer, usually methyl methacrylate. MABS is an amorphous, clear, transparent material with thermal and mechanical properties like ABS. The transparency is achieved by matching the refractive indices of the matrix resin (the transparent acrylate—acrylonitrile—styrene polymer) with the polybutadiene rubber impact modifier. MABS has the highest impact resistance of all the styrenic plastics. Sometimes called transparent... [Pg.48]

Engineering plastic n. (1) A broad term covering those plastics, with or without fillers and reinforcements that have mechanical, chemical, electrical, and/or thermal properties suitable for industrial applications. R. B. Seymour, an outstanding authority, defined them as polymers thermoplastic or thermosetting, that maintain their dimensional stability and major mechanical properties in the temperature range 0-100° C. He listed the big five (among neat resins) as nylons, polycarbonate, acetals, polyphenylene ether, and thermoplastic polyesters. Among many others are acrylics, fluorocarbons, phenoxy, acrylonitrile-butadiene-styrene terpolymer, polyaryl... [Pg.360]

Pdymerizations conducted so far have produced polymer coatii wifii a wi range of chemical and mechanical properties vtdiidi could be used to modify the carbon fiber-polymer matrix interphase of comptmt Helmed from fibers trrated by electropolymerization. A flexible polymer interphase could be introduced using systems such as methyl acrylate or VTBN, while stiffness could be adueved by using the styrene or styrene-acrylonitrile systems. Methyl methacrylate and styrene monomers would be expected to yield linear uncrosslinked polymer coatings while monomers which are multifunctional such as A,A -methylenebisacryiamide or multifunctional aziridines would be expected to crosslink in the systems they were used in. [Pg.49]

The partial substitution of styrene by acrylates lowers the viscosity, and provides better adhesion to the fiber in composites. Acrylonitrile imparts exceptional mechanical properties and increases both hardness and impact strength. The propylene glycol based UP with 40 % styrene has an impact strength of 14 J/m-width, and an addition of 20 % acrylonitrile increases it to 39 J/m-width. The addition of 11 % acrylonitrile increases hardness from 12 BUN to 26 BUN [7]. [Pg.2]


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See also in sourсe #XX -- [ Pg.9 ]




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Acrylate-styrene-acrylonitrile

Acrylic styrene

Acrylics mechanical

Acrylonitrile mechanism

STYRENE-ACRYLONITRILE

Styrene mechanism

Styrene properties

Styrene-acrylonitrile mechanical properties

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