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Impact polystyrene rubber particles

Crosslinking Reactions in High Impact Polystyrene Rubber Particles... [Pg.163]

Impact polystyrene contains polybutadiene added to reduce brittleness. The polybutadiene is usually dispersed as a discrete phase in a continuous polystyrene matrix. Polystyrene can be grafted onto rubber particles, which assures good adhesion between the phases. [Pg.1023]

The rubber particles should not be so small that they are completely embedded in a craze. It is interesting to note that in high-impact polystyrene crazes tend to be about 2 p.m thick and the optimum particle sizes observed as a result of experience are quoted in the range 1-10 p.m. For ABS the figures are about 0.5 p.m and 0.1-l.Op.m respectively. [Pg.57]

Rubber toughened polystyrene is widely used in electronic and kitchen appliances. This type of application requires a good balance of stiffness, impact resistance, and ready coloration. Telephones, which are frequently dropped, are an excellent example of the benefits of rubber toughened polystyrene. The high surface gloss that we desire is obtained by minimizing the size of the rubber particles. Larger items, such as canoes, can be thermoformed from extruded sheet. [Pg.340]

Transition from liquid behavior to solid behavior has been reported with fine particle suspensions with increased filler content in both Newtonian and non-Newtonian liquids. Industrially important classes are rubber-modified polymer melts (small rubber particles embedded in a polymer melt), e.g. ABS (acrylo-nitrile-butadiene-styrene) or HIPS (high-impact polystyrene) and fiber-reinforced polymers. Another interesting suspension is present in plasticized polyvinylchloride (PVC) at low temperatures, when suspended PVC particles are formed in the melt [96], The transition becomes evident in the following... [Pg.206]

The major weaknesses of polystyrene are brittleness, and softening in hot water. Brittleness is remedied by dissolving 2-10 percent of rubber in styrene monomer before polymerization, producing high-impact styrene (HIPS), in which 10- xm rubber particles improve impact strength by an order of magnitude, with some sacrifice of other mechanical properties and transparency this accounts for more than half of the total polystyrene market. [Pg.645]

There are some additional applications of the theory which are presently under investigation. These are the effects of drawing on fibers for which the three-dimensional theory with transverse symmetry is applicable and the toughening mechanism in high impact polystyrene for which the flaw spectrum may be viewed as caused by the size, orientation, and spacing distributions of the rubber particles. [Pg.66]

Van Henten, at the Shell Plastic Laboratories (II), showed that styrene-butadiene block polymers can be blended with commercial HIPS to upgrade its impact strength to 5.8 ft-lbs/inch. Childers, at Phillips Petroleum (12), blended commercial polystyrene with block polymers in a Brabender plastograph. To control rubber particle size he added a peroxide during the blending operation, thereby creating crosslinks. With this technique he achieved an impact strength of 5.9 ft-lbs/inch. [Pg.243]

It is well known that systems like polystyrene or polystyrene-acrylonitrile—generally considered brittle materials—have a remarkable increase in toughness and resistance to impact when polyblended with finely dispersed, crosslinked, but partly compatible, rubber particles. These particles are generally 0.1-10 fi in size and frequently consist of butadiene which has been grafted with monomers of similar composition to the matrix or continuous phase. [Pg.288]

Bucknall and Smith (17) concluded that crazing is the dominant mechanism to toughen high impact polystyrene and related polymers. One important function of the rubber particles is to serve as craze initiators and stabilizers in the glassy matrix. However Newman and Strella (18) concluded from optical microscope studies that cold drawing is responsible for toughness in ABS. [Pg.343]

High Impact Polystyrene (UPS) obtained by means of copolymerization of styrene with rubber represents heterogeneous system consisting of polystyrene matrix and the particles of rubber phase dispersed in it the particles in their turn keep the graft copolymer and a great number of occluded polystyrene O/,Physical and mechanical properties of HIPS are defined... [Pg.379]

In 1954, Dow finally perfected a can process to make high-impact polystyrene (HIPS). The secret was that the traditional can process could not simply be used since the product would be full of gel particles of rubber ( fish-eyes ) instead, the styrene-rubber mixture was first carried out to 30% conversion with shearing agitation. Then the mixture was transferred to 10 gallon cans where the reaction was completed. This process was documented in the now famous Amos patent [18]. [Pg.18]

To overcome the brittleness of GPPS, the material was modified by incorporation of polybutadiene. Impact-modified polystyrene (IPS) was invented by Ostromislensky [1] and has been commercialized since the 1950s. IPS consists of a polystyrene matrix with embedded cellular rubber particles. By rubber... [Pg.25]

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... [Pg.425]


See other pages where Impact polystyrene rubber particles is mentioned: [Pg.263]    [Pg.419]    [Pg.507]    [Pg.257]    [Pg.671]    [Pg.71]    [Pg.330]    [Pg.338]    [Pg.276]    [Pg.475]    [Pg.419]    [Pg.115]    [Pg.118]    [Pg.232]    [Pg.237]    [Pg.238]    [Pg.161]    [Pg.385]    [Pg.30]    [Pg.160]    [Pg.38]    [Pg.706]    [Pg.136]    [Pg.248]    [Pg.287]    [Pg.204]    [Pg.310]    [Pg.321]    [Pg.420]    [Pg.591]    [Pg.594]    [Pg.633]    [Pg.474]    [Pg.507]   
See also in sourсe #XX -- [ Pg.223 , Pg.226 ]




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