High-impact polystyrene-poly

Structural Components. In most appHcations stmctural foam parts are used as direct replacements for wood, metals, or soHd plastics and find wide acceptance in appHances, automobUes, furniture, materials-handling equipment, and in constmction. Use in the huil ding and constmction industry account for more than one-half of the total volume of stmctural foam appHcations. High impact polystyrene is the most widely used stmctural foam, foUowed by polypropylene, high density polyethylene, and poly(vinyl chloride). The constmction industry offers the greatest growth potential for ceUular plastics. 

The oxidative coupling of 2,6-dimethylphenol to yield poly(phenylene oxide) represents 90—95% of the consumption of 2,6-dimethylphenol (68). The oxidation with air is catalyzed by a copper—amine complex. The poly(phenylene oxide) derived from 2,6-dimethylphenol is blended with other polymers, primarily high impact polystyrene, and the resulting alloy is widely used in housings for business machines, electronic equipment and in the manufacture of automobiles (see Polyethers, aromatic). A minor use of 2,6-dimethylphenol involves its oxidative coupling to... 

Hexamethylphosphoramide (HMPT), 185 HFBPA-based poly(arylene ether)s, 362 HFCs. See Hydrofluorocarbons (HFCs) High-impact polystyrene (HIPS), 219 High-melting polymers, 33 High-melting-point fiber-forming polyesters, 19... 

HIPS High-impact polystyrene PECT Poly (ethylene-co-1,4-cyclohexane-... 

Poly(2,6-dimethyl-l,4-phenylene oxide)/ high impact polystyrene (PPO/HIPS), 20 360... 

Polycarbonate is blended with a number of polymers including PET, PBT, acrylonitrile-butadiene-styrene terpolymer (ABS) rubber, and styrene-maleic anhydride (SMA) copolymer. The blends have lower costs compared to polycarbonate and, in addition, show some property improvement. PET and PBT impart better chemical resistance and processability, ABS imparts improved processability, and SMA imparts better retention of properties on aging at high temperature. Poly(phenylene oxide) blended with high-impact polystyrene (HIPS) (polybutadiene-gra/f-polystyrene) has improved toughness and processability. The impact strength of polyamides is improved by blending with an ethylene copolymer or ABS rubber. 

High-impact polystyrene (HIPS) is produced by polymerizing styrene in the presence of a rubber, usually poly(l,3-butadiene). HIPS has improved impact resistance compared to polystyrene and competes with ABS products at low-cost end applications such as fast-food cups, lids, takeout containers, toys, kitchen appliances, and personal-care product containers. HIPS as well as ABS and SMA are used in physical blends with other polymers, such as polycarbonates, polyesters, and polyamides, to improve impact resistance (Sec. 2-13c-3). 

Although this method yields a mixture of homopolymer and graft copolymer, and probably also ungrafted backbone polymer, some of the systems have commercial utility. These are high-impact polystyrene (HIPS) [styrene polymerized in the presence of poly(l,3-buta-diene)], ABS and MBS [styrene-acrylonitrile and methyl methacrylate-styrene, respectively, copolymerized in the presence of either poly(l,3-butadiene) or SBR] (Sec. 6-8a). 

As of this date, there is no lithium or alkyl-lithium catalyzed polyisoprene manufactured by the leading synthetic rubber producers- in the industrial nations. However, there are several rubber producers who manufacture alkyl-lithium catalyzed synthetic polybutadiene and commercialize it under trade names like "Diene Rubber"(Firestone) "Soleprene"(Phillips Petroleum), "Tufdene"(Ashai KASA Japan). In the early stage of development of alkyl-lithium catalyzed poly-butadiene it was felt that a narrow molecular distribution was needed to give it the excellent wear properties of polybutadiene. However, it was found later that its narrow molecular distribution, coupled with the purity of the rubber, made it the choice rubber to be used in the reinforcement of plastics, such as high impact polystyrene. Till the present time, polybutadiene made by alkyl-lithium catalyst is, for many chemical and technological reasons, still the undisputed rubber in the reinforced plastics applications industries. 

A.B. Boscoletto, M. Checchin, L. Milan, P. Pannocchia, M. Tavan, G. Camino, and M.P. Luda, Combustion and fire retardance of poly-(2,6-dimethyl-l,4-phenylene ether)-high-impact polystyrene blends. II. Chemical aspects,/. Appl. Polym. Sci., 67(13) 2231-2244,1998. 

Typical physical properties for an injection-molded transparent acrylic polyblend resin are given in Table II. The injection molding conditions used are given in Table III. Tensile, flexural, and impact properties are within the range reported for typical ABS and high impact polystyrene resins. Optical properties approach those of the acrylics [i.e., poly (methyl methacrylate)]. The strength properties are on the low side of those reported in the first paper for the transparent diene... 

ABA ABS ABS-PC ABS-PVC ACM ACS AES AMMA AN APET APP ASA BR BS CA CAB CAP CN CP CPE CPET CPP CPVC CR CTA DAM DAP DMT ECTFE EEA EMA EMAA EMAC EMPP EnBA EP EPM ESI EVA(C) EVOH FEP HDI HDPE HIPS HMDI IPI LDPE LLDPE MBS Acrylonitrile-butadiene-acrylate Acrylonitrile-butadiene-styrene copolymer Acrylonitrile-butadiene-styrene-polycarbonate alloy Acrylonitrile-butadiene-styrene-poly(vinyl chloride) alloy Acrylic acid ester rubber Acrylonitrile-chlorinated pe-styrene Acrylonitrile-ethylene-propylene-styrene Acrylonitrile-methyl methacrylate Acrylonitrile Amorphous polyethylene terephthalate Atactic polypropylene Acrylic-styrene-acrylonitrile Butadiene rubber Butadiene styrene rubber Cellulose acetate Cellulose acetate-butyrate Cellulose acetate-propionate Cellulose nitrate Cellulose propionate Chlorinated polyethylene Crystalline polyethylene terephthalate Cast polypropylene Chlorinated polyvinyl chloride Chloroprene rubber Cellulose triacetate Diallyl maleate Diallyl phthalate Terephthalic acid, dimethyl ester Ethylene-chlorotrifluoroethylene copolymer Ethylene-ethyl acrylate Ethylene-methyl acrylate Ethylene methacrylic acid Ethylene-methyl acrylate copolymer Elastomer modified polypropylene Ethylene normal butyl acrylate Epoxy resin, also ethylene-propylene Ethylene-propylene rubber Ethylene-styrene copolymers Polyethylene-vinyl acetate Polyethylene-vinyl alcohol copolymers Fluorinated ethylene-propylene copolymers Hexamethylene diisocyanate High-density polyethylene High-impact polystyrene Diisocyanato dicyclohexylmethane Isophorone diisocyanate Low-density polyethylene Linear low-density polyethylene Methacrylate-butadiene-styrene... 

Note ABS, acrylonitrile/butadiene/styrene EPS, expandable polystyrene HIPS, high-impact polystyrene PA, polyamide PBT, poly(butylene)terephthalate PC, polycarbonate PE, polyethylene PET, poly(ethylene)terephthalate PP, polypropylene PUR, polyurethane PVC, polyvinylchloride UPE, unsaturated polyester Textile, textile application. 

The phase relationships of two-phase polymer systems also have been of considerable interest in recent years. In an important series of papers, Molau and co-workers (19-24) studied systems, which were denoted POO emulsions (polymeric oil-in-oil), prepared by dissolving a given polymer in monomer and then polymerizing the monomer. During polymerizations of this type the composition of the respective phases reverses, and a phase inversion process was proposed to explain this. A similar process has been suggested as the mechanism by which poly-butadiene forms the dispersed phase in the manufacture of high-impact polystyrenes (22,25). Recently, Kruse has pointed out that this phase-inversion point may correspond to that point on a ternary phase diagram at which the reaction line bisects a tie line (26), and we have advanced a similar point of view in our earlier reports (17,18, 27). 

M. Azhar Uddin, T. Bhaskar, J. Kaneko, A. Muto, Y. Sakata, and T. Matsui, Dehy-drohalogenation during pyrolysis of brominated flame retardant containing high impact polystyrene (HIPS-Br) mixed with poly(vinyl chloride). Fuel., 81, 1819-1825 (2002). 

Craze formation is a dominant mechanism in the toughening of glassy polymers by elastomers in polyblends. Examples are high-impact polystyrene (HIPS), impact poly(vinyl chloride), and ABS (acrylonitrile-butadiene-styrene) polymers. Polystyrene and styrene-acrylonitrile (SAN) copolymers fracture at strains of 10 , whereas rubber-modified grades of these polymers (e.g., HIPS and ABS) form many crazes before breaking at strains around 0.5. Rubbery particles in... 

HIPS high-impact polystyrene or poly(butadiene-co-styrene) PP polypropylene... 

Polymers derived from polystyrene but having alkyl or aryl groups substituted at the benzene ring were synthesized in an effort to improve some of polystyrene properties such as the impact resistance and obtain qualities similar to those achieved using copolymers with 1,3-butadiene (high impact polystyrene or HIPS). The polymers included In this class are poly(3-methylstyrene), poly(4-methylstyrene) CAS 24936-41-2, poly(4-phenylstyrene) CAS 25232-08-0 [115], as well as poly(2-vinylnaphthalene) CAS 28406-56-6. Some of the reports regarding thermal decomposition of these polymers are summarized in Table 6.2.10. 

Since this paper will be restricted to sequential IPN s based on cross-poly butadiene-inter-cross-polystyrene. PB/PS, it is valuable to examine the range of possible compositions, see Figure 2 ( ). The PB/PS IPN polymer pair models high-impact polystyrene, and in fact, many of the combinations made are actually more impact resistant than the commercial materials. In general, with the addition of crosslinks, especially in network I, the phase domains become smaller. The impact resistance of high-impact polystyrene, upper left, is about 80 J/ra. In the same experiment, the semi-I IPN, middle left is about 160 J/m, and the full IPN, lower left, is about 265 J/m (g). Since the commercial material had perhaps dozens of man-years of development, and the IPN composition was made simply for doctoral research with substantially no optimization, it was obvious that these materials warranted further study. 

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