Polystyrene melting point

Steam-Chest Expansion. In steam-chest expansion the resin beads in which gas is already present are poured into molds into which steam is injected. The steam increases the temperature close to the melting point and expands within the stmcture to create beads with food cushioning and insulating properties. Expanded polystyrene is widely used in this process for thermal insulation of frozen food packaging. 

The thermoplastic or thermoset nature of the resin in the colorant—resin matrix is also important. For thermoplastics, the polymerisation reaction is completed, the materials are processed at or close to their melting points, and scrap may be reground and remolded, eg, polyethylene, propjiene, poly(vinyl chloride), acetal resins (qv), acryhcs, ABS, nylons, ceUulosics, and polystyrene (see Olefin polymers Vinyl polymers Acrylic ester polymers Polyamides Cellulose ESTERS Styrene polymers). In the case of thermoset resins, the chemical reaction is only partially complete when the colorants are added and is concluded when the resin is molded. The result is a nonmeltable cross-linked resin that caimot be reworked, eg, epoxy resins (qv), urea—formaldehyde, melamine—formaldehyde, phenoHcs, and thermoset polyesters (qv) (see Amino resins and plastics Phenolic resins). 

In the crystalline region isotactic polystyrene molecules take a helical form with three monomer residues per turn and an identity period of 6.65 A. One hundred percent crystalline polymer has a density of 1.12 compared with 1.05 for amorphous polymer and is also translucent. The melting point of the polymer is as high as 230°C. Below the glass transition temperature of 97°C the polymer is rather brittle. 

The processing of blends of an amorphous material (polystyrene) and a crystalline material with a high melting point (PPO) reflects the nature of the constituent materials. The processing is mainly by injection moulding, and the major points to be considered when processing Noryl-type materials are ... 

Methylpentene polymer, a light plastic, has a crystalline melting point of 464 retention up to 392° F, transparency of 92%, and electrical properties similar to fluoroethylene. Its impact strength is greater than polystyrene and polymethyl methacr resistant to alkalies, weak acids, and non-chlorinated solvents. It may be injection m< implements for food packaging and preparation, medical care, and non-stick coating ... 

Modification of filler s surface by active media leads to the same strong variation in viscosity. We can point out as an example the results of work [8], in which the values of the viscosity of dispersions of CaC03 in polystyrene melt were compared. For q> = 0.3 and the diameter of particles equal to 0.07 nm a treatment of the filler s surface by stearic acid caused a decrease in viscosity in the region of low shear rates as compared to the viscosity of nontreated particles more than by ten times. This very strong result, however, should not possibly be understood only from the point of view of viscometric measurements. The point is that, as stated above, a treatment of the filler particles affects its ability to netformation. Therefore for one and the same conditions of measuring viscosity, the dispersions being compared are not in equivalent positions with respect to yield stress. Thus, their viscosities become different. 

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... 

Syndiotactic polystyrene is a new polymeric material150 152 of industrial relevance since it shows a high melting point (270°C) and high crystallization rates.153 Syndiotactic polystyrene is a highly stereoregular polymer which can be obtained by using several soluble titanium and, to a less extent, zirconium compounds. 

As polystyrene obtained by free radical polymerisation technique is atactic it is therefore non-crystalline. The isotactic polystyrene is obtained by the use of Ziegler-Natta catalysts and n-butyl lithium. Isotactic polystyrene is having a high crystalline Melting point of 250°C. It is transparent. It is more brittle than the atactic polymer. 

Staudinger, the final speaker, presented a broad array of data on polymerization, hydrogenation, comparisons of viscosity, melting points, and solubility of polymers. He pointed out that in the conversion of polystyrene to hexahydropolystyrene, and polyindene into hexahydropolyindene, the products retained their high molecular weight properties. Again, he maintained this proved "the monomers are united by main valencies" (62). 

Fig. 1.10. Birefringence in the 1—3 plane vs. shear stress, for a polystyrene melt (Styron 666) at 190° C. Full line nu—nn, as calculated according to eq. (1.21) from the points of Fig. 1.9. (o) u — n a, as calculated from cone-and-plane measurements in the 1—2 plane, using eq. (1.23)...

Commercial polystyrene, one of the most representative general-purpose resins, is an amorphous atactic polymer with no melting point (softening temperature ca 100 °C, glass transition temperature ca 70-100 °C). Since the discovery of Ziegler-Natta catalysts, many efforts to produce stereoregular polystyrenes have been made. 

Fig. 2. Temperature dependence of intensity of fluorescence of auramine O in polystyrene film open circles, heating from room temperature to the melting point filled circles, cooling and solidifying the melt (70)...

Isotactic Polystyrene. The familiar steam molding of pre-expanded particles has so far not been applied successfully to isotactic polystyrene. However, the polymer has been foamed, according to three disclosed methods. For example, finely divided acetone-insoluble polymer, with a melting point in excess of 200°C., is blended with a liquid selected from methylene chloride, aromatic hydrocarbons, or halogenated aromatic hydrocarbons. This blend is then heated (84). A mixture of molten polymer and methyl chloride, propane, or butane is suddenly depressurized (8). Foam may also be generated in a continuous manner directly from a butyllithium-initiated polymerization conducted in the presence of a 4/1 blend of benzene and petroleum ether (15). 

Polymers can also lack rotational freedom because of steric hindrance associated with the functional groups attached to the back- j bone. We know thinking is a bit of an effort, but the two missing melting temperatures are I 170°C and 225°C (Figure 10-50). Which y one of these is the melting point of isotactic polystyrene ... 

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