Acrylonitrile-butadiene-styrene adhesives

The homopolymers, which are formed from alkyl cyanoacrylate monomers, are inherently brittle. For applications which require a toughened adhesive, rubbers or elastomers can be added to improve toughness, without a substantial loss of adhesion. The rubbers and elastomers which have been used for toughening, include ethylene/acrylate copolymers, acrylonitrile/butadiene/styrene (ABS) copolymers, and methacrylate/butadiene/styrene (MBS) copolymers. In general, the toughening agents are incorporated into the adhesive at 5-20 wt.% of the monomer. 

Uses Copolymerized with methyl acrylate, methyl methacrylate, vinyl acetate, vinyl chloride, or 1,1-dichloroethylene to produce acrylic and modacrylic fibers and high-strength fibers ABS (acrylonitrile-butadiene-styrene) and acrylonitrile-styrene copolymers nitrile rubber cyano-ethylation of cotton synthetic soil block (acrylonitrile polymerized in wood pulp) manufacture of adhesives organic synthesis grain fumigant pesticide monomer for a semi-conductive polymer that can be used similar to inorganic oxide catalysts in dehydrogenation of tert-butyl alcohol to isobutylene and water pharmaceuticals antioxidants dyes and surfactants. 

Acrylonitrile-Butadiene-Styrene (ABS). ABS plastics are derived from acrylonitrile, butadiene, and styrene. ABS materials have a good balance of physical properties. There are many ABS modifications and many blends of ABS with other thermoplastics that can affect adhesion properties. ABS resin can be bonded to itself and to other materials with adhesives, by solvent cementing, or by thermal welding. 

Butadiene is used as a chemical intermediate and as a polymer component in the synthetic rubber industry, the latter accounting for 75% of the butadiene produced. Styrene-butadiene rubber, polybutadiene rubber, adiponitrile, styrene-butadiene latex, acrylonitrile-butadiene-styrene resins, and nitrile rubber are used in the manufacture of tires, nylon products, plastic bottles and food wraps, molded rubber goods, latex adhesives, carpet backing and pads, shoe soles, and medical devices. 

FDA approved under 21CFR178.2010 for use in acrylonitrile-butadiene-styrene copolymers at levels not to exceed 0.6% by weight of the copolymer. Section 177.1010 for use in semi-rigid and rigid acrylics at levels not to exceed 0.1% by weight of the plastic, and Section 175.105 as a component of food packaging adhesives. Also, approved by the FDA as an antioxidant in the preparation of rubber articles at a level not to exceed 5% by 21CFR177.2600. 

The primary use of TBBPA is as a flame retardant in epoxy resin circuit boards and in electronic enclosures made of polycarbonate-acrylonitrile-butadiene-styrene (PC-ABS). Other applications of TBBPA include its use as a flame retardant for plastics, paper, and textiles as a plasticizer in adhesives and coatings and as a chemical intermediate for the synthesis of other flame retardants (e.g., TBBPA allyl ether). It is also been applied to carpeting and office furniture as a flame retardant. 

The microphase structure and mechanical properties of the blends containing neat acrylonitrile-butadiene-styrene copolymer (ABS), styrene-acrylonitrile copolymer (SAN) and sodium sulfonated SAN ionomer have been investigated as a function of ion content of the ionomer in the blend by Park et a/.51 The interfacial adhesion was quantified by H NMR solid echo experiments. The amount of interphase for the blend containing the SAN ionomer with low ion content (3.1 mol%) was nearly the same as that of ABS, but it decreases with the ion content of the ionomer for the blend with an ion content greater than 3.1 mol%. Changing the ionomer content in the blends shows a positive deviation from the rule of mixtures in tensile properties of the blends containing the SAN ionomer with low ion content. This seems to result from the enhanced tensile properties of the SAN ionomer, interfacial adhesion between the rubber and matrix, and the stress concentration effect of the secondary particles. 

In rubber-modified polymers like high impact polystyrene or acrylonitrile-butadiene-styrene (ABS) resins, the toughening effect of the dispersed rubber particles appears only in the presence of block or graft copolymers. These copolymers regulate the particle size of the rubber dispersion and achieve adhesion of the two phases. Hence, graft copolymers are of practical importance in polymer alloys. 

In heterophase polymeric materials such as rubber modified polystyrene or acrylonitrile-butadiene-styrene (ABS) resins, outstanding mechanical properties can be obtained only by regulating the dispersed rubber particle size and by achieving adhesion between the rubber and the resin phase. This can usually be achieved by adding block or graft copolymers, or by their formation in situ, as in industry. 

Tritolyl phosphate (TTP) has been examined as a pretreatment for E-glass in epoxide laminates and thermoplastic adhesives for bonding poly(vinyl chloride) to aluminum, steel to zinc, and acrylonitrile butadiene styrene to aluminum [59]. Mono- and diphosphate esters have been claimed to be suitable adhesion-promoting primers for acrylic adhesives on metal [60,61], unsaturated acid phosphates have been suggested as primers for use on metals to be bonded with free radical initiated adhesives [42], and thiopho-sphate esters have been suggested for adhesives to be used on plastics, ceramics, and metals [62]. 

The wide variety of applications of anaerobic adhesives and sealants is made possible by the modifications that make the viscosity appropriate to the application. An application that requires penetration into close-fitting parts should have very low viscosity, while a produet used with large, loose-fitting parts should have a high viscosity. A styrene aerylate eopolymer could be used to increase the viscosity [59]. Polymethacrylates, eellulose esters, butadiene-styrene eopolymers, acrylonitrile-butadiene-styrene copolymers, poly(vinyl ehloride), copolymers of vinyl chloride and vinyl acetate, poly(vinyl aeetate), eellulose ethers, polyesters, polyurethanes, and other thermoplastic resins have also been used to eontrol the flow eharacteristics of anaerobic sealants [60]. The flow eharaeteristies of anaerobic formulations can also be controlled by the addition of fumed siliea and other solid additives whieh can impart thixotropic properties [61]. 

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. 

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