HIPS High Impact Polystyrene

HIPS with different types of rubber particles  

HIPS with rubber-shell (core-shell) particles  

HIPS with salami particles of EPT (ethylene-propylene terpolymer)  

PB phase brighter than PS matrix quick SEM inspection of rubber particles in chemically stained surface layers [3]  

The story of these systems begins as long ago as 1925. Ostromislensky [70] of Naugatuck Chemical filed a patent application for the polymerization of a natural rubber solution in styrene. This produced a tough white thermoplastic in the place of a brittle, glassy, transparent 

The morphology of high-impact polystyrene may be complex and the rubber globules may contain polystyrene inclusions. Its color is white rather than transparent like polystyrene, presumably because of light scattering by the dispersed polybutadiene globules, which have a different refractive index from the polystyrene matrix. 

There have been investigations showing that variables such as polymerization initiator, mixing conditions, and rubber particle size influence the level of enhancement of properties. 

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Polystyrene. Polystyrene [9003-53-6] is a thermoplastic prepared by the polymerization of styrene, primarily the suspension or bulk processes. Polystyrene is a linear polymer that is atactic, amorphous, inert to acids and alkahes, but attacked by aromatic solvents and chlorinated hydrocarbons such as dry cleaning fluids. It is clear but yellows and crazes on outdoor exposure when attacked by uv light. It is britde and does not accept plasticizers, though mbber can be compounded with it to raise the impact strength, ie, high impact polystyrene (HIPS). Its principal use in building products is as a foamed plastic (see Eoamed plastics). The foams are used for interior trim, door and window frames, cabinetry, and, in the low density expanded form, for insulation (see Styrene plastics). 

Because of such desirable characteristics as low cost, good mouldability, excellent colour range, transparency, rigidity and low water absorption, polystyrene became rapidly developed. For many purposes, however, it was considered to be unacceptably brittle and this led to the development of the rubber-modified high-impact polystyrene (HIPS) and to the complex ABS, AMBS and... 

High-impact Polystyrenes (HIPS) (Toughened Polystyrenes (TPS)) 437... 

HIGH-IMPACT POLYSTYRENE (HIPS) (TOUGHENED POLYSTYRENES (TPS))... 

In the late 1940s, the demand for styrene homopolymers (PS) and styrene-acrylonitrile copolymers (SAN) was drastically reduced due to their inherent brittleness. Thus, the interest was shifted to multiphase high-impact polystyrene (HIPS) and rubber-modified SAN (ABS). In principle, both HIPS and ABS can be manufactured by either bulk or emulsion techniques. However, in actual practice, HIPS is made only by the bulk process, whereas ABS is produced by both methods [132,133]. 

The formation of the polyalloy results in improvement in the performance of the blends. This system is similar to the production of high-impact polystyrene (HIPS) where a rubber is dissolved in styrene monomer and then polymerized in the usual way. Even though the impact strength of the compatibilized PS-PE blend was higher than that of PS, it was much less than that of HIPS. In another study. Van Ballegooie and [55] have confirmed... 

Polystyrene (PS) The volume of expanded polystyrene produced probably exceeds the volume production of all other plastics (excluding the polyurethanes) put together. At least half the weight of polystyrene produced is in the form of high impact polystyrene (HIPS)—a complex blend containing styrene-butadiene rubber or polybutadiene. 

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... 

High-temperature solution reactions, 75 HIPS. See High-impact polystyrene (HIPS)... 

Unit Ratio Material Balance for High Impact Polystyrene (HIPS) 0.912 if Styrene... 

SEM and transmission electron microscopy (TEM) are employed to examine materials for the presence and distribution of impact modifiers such as polybutadiene rubber in high impact polystyrene (HIPS) and methacrylate butadiene styrene terpolymer in PVC. Quantification is either by transmission IR spectroscopy against standards or nuclear magnetic resonance (NMR) spectroscopy. 

High impact polystyrene (HIPS), 11 466 20 353, 359-360 23 359, 368 antioxidant applications, 3 121 surface appearance of, 23 363-364 thermoforming of, 23 398—399 High intensity cross-belt magnetic separators, 15 454-455 High intensity dry magnetic separators, 15 450—452... 

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). 

Preparation of a Polystyrene/Polybutadiene-Blend (High Impact Polystyrene, HIPS) by Polymerization of Styrene in the Presence of Polybutadiene... 

Figure 5.84 Stress-strain curves for polystyrene (PS) and high-impact polystyrene (HIPS). Reprinted, by permission, from N. G. McCrum, C. P. Buckley, and C. B. Bucknall, Principles of Polymer Engineering, 2nd ed., p. 200. Copyright 1997 by Oxford University Press.

The term graft copolymer is used to describe copolymers with long sequences of another monomer (comonomer) as branches on the main polymer chain. Most commercial varieties of high-impact polystyrene (HIP) and copolymers of acrylonitrile, butadiene, and styrene (ABS) are graft copolymen in which the main polymer chain is polybutadiene and the branches are styrene, or styrene and acrylonitrile. Figure 1.12 shows various types of copolymers. 

PBDEs are used in different resins, polymers, and substrates at levels ranging from 5 to 30% by weight (EU 2001). Plastic materials that utilize PBDEs as flame retardants include ABS polyacrylonitrile (PAN) polyamide(PA) polybutylene terephthalate (PBT) polyethylene (PE) cross-linked polyethylene (XPE) polyethylene terephthalate (PET) polypropylene (PP) polystyrene (PS) high-impact polystyrene (HIPS) polyvinyl chloride (PVC) polyurethane (PUR) and unsaturated polyester (UPE). These polymers and examples of their final products are summarized inTable 5-2 (Hardy 2002 WHO 1994a). 

B.J. Jody, B. Arman, D.E. Karvelas, J.A. Pomykala, Jr., and E.J. Daniels, Method for the separation of high impact polystyrene (HIPS) and acrylonitrile butadiene styrene (ABS) plastics, US Patent 5 653867, assigned to The University of Chicago (Chicago, IL), August 5,1997. 

M.A. Uddin, T. Bhaskar, J. Kaneko, A. Muto, Y. Sakata, and T. Matsui, Dehydrohalogenation during pyrolysis of brominated flame retardant containing high impact polystyrene (HIPS-Br) mixed with polyvinylchloride (PVC), Fuel, 81(14) 1819-1825, September 2002. 

Order-disorder transitions and spinodals were computed for linear multi block copolymers with differing sequence distributions by Fredrickson et al. (1992). This type of copolymer includes polyurethanes, styrene-butadiene rubber, high impact polystyrene (HIPS) and acrylonitrile-butadiene-styrene (ABS) block copolymers. Thus the theory is applicable to a broad range of industrial thermoplastic elastomers and polyurethanes. The parameter... 

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