| Polystyrene | |
|---|---|
| Density | 1050 kg/m³ |
| Electrical conductivity (σ) | 10-16 S/m |
| Thermal conductivity | 0.08 W/(m·K) |
| Young's modulus (E) | 3000-3600 MPa |
| Tensile strength (σt) | 46–60 MPa |
| Elongation at break | 3–4% |
| Notch test | 2–5 kJ/m² |
| Glass temperature | 95 °C |
| Melting point | 240 °C |
| Vicat B | 90 °C |
| Heat transfer coefficient (λ) | 0.17 W/(m·K) |
| Linear expansion coefficient (α) | 8 10-5 /K |
| Specific heat (c) | 1.3 kJ/(kg·K) |
| Water absorption (ASTM) | 0.03–0.1 |
| source: A.K. van der Vegt & L.E. Govaert, Polymeren, | |
| van keten tot kunstof, ISBN 90-407-2388-5 | |
Polystyrene is a polymer made from the monomer styrene, a liquid hydrocarbon that is commercially manufactured from petroleum. At room temperature, polystyrene is normally a solid thermoplastic, but can be melted at higher temperature for molding or extrusion, then resolidified. Styrene is an aromatic monomer, and polystyrene is an aromatic polymer.
Polystyrene was accidentally discovered in 1839 by Eduard Simon, an apothecary in Berlin, Germany. From storax, the resin of Liquidambar orientalis, he distilled an oily substance, a monomer which he named styrol. Several days later Simon found that the styrol had thickened, presumably due to oxidation, into a jelly he dubbed styrol oxide ("Stryroloxyd"). By 1845 English chemist John Blyth and German chemist August Wilhelm von Hofmann showed that the same transformation of styrol took place in the absence of oxygen. They called their substance metastyrol. Analysis later showed that it was chemically identical to Styroloxyd. In 1866 Marcelin Berthelot correctly identified the formation of metastyrol from styrol as a polymerization process. About 80 years went by before it was realized that heating of styrol starts a chain reaction which produces macromolecules, following the thesis of German organic chemist Hermann Staudinger (1881 - 1965). This eventually led to the substance receiving its present name, polystyrene. The I.G. Farben company began manufacturing polystyrene in Ludwigshafen, Germany, about 1931, hoping it would be a suitable replacement for die cast zinc in many applications. Success was achieved when they developed a reactor vessel that extruded polystyrene through a heated tube and cutter, producing polystyrene in pellet form.
Pure solid polystyrene is a colorless, hard plastic with limited flexibility. It can be cast into molds with fine detail. Polystyrene can be transparent or can be made to take on various colors. It is economical and is used for producing plastic model assembly kits, plastic cutlery, CD "jewel" cases, and many other objects where a fairly rigid, economical plastic of any of various colors is desired.
Polystyrene fabricated into a sheet can be stamped (formed) into economic, disposable cups, glasses, bowls, lids, and other items, especially when high strength, durability, and heat resistance are not essential. A thin layer of transparent polystyrene is often used as an infra-red spectroscopy standard.
Expanded polystyrene used to contain CFCs, but other, more environmentally-safe blowing agents are now used. Because it is an aromatic hydrocarbon, it burns with an orange-yellow flame, giving off soot, as opposed to non-aromatic hydrocarbon polymers such as polyethylene, which burn with a light yellow flame (often with a blue tinge) and no soot.
Production methods include sheet stamping (PS) and injection molding (both PS and HIPS).
The chemical makeup of polystyrene is a long chain hydrocarbon with every other carbon connected to a Phenyl group (an aromatic ring similar to benzene.
A 3-D model would show that each of the chiral backbone carbons lies at the center of a tetrahedron, with its 4 bonds pointing toward the vertices. Say the -C-C- bonds are rotated so that the backbone chain lies entirely in the plane of the diagram. From this flat schematic, it isn't evident which of the phenyl (benzene) groups are angled toward us from the plane of the diagram, and which ones are angled away. The isomer where all of them are on the same side is called isotactic polystyrene, which isn't produced commercially. Ordinary atactic polystyrene has these large phenyl groups randomly distributed on both sides of the chain. This random positioning prevents the chains from ever aligning with sufficient regularity to achieve any crystallinity, so the plastic has no melting temperature, Tm. But metallocene-catalyzed polymerization can produce an ordered syndiotactic polystyrene with the phenyl groups on alternating sides. This form is highly crystalline with a Tm of 270°C.
The Unicode character is U+9848, which will appear here if you have a suitable font installed: ♸.
Acrylonitrile butadiene styrene or ABS plastic is similar to HIPS: a copolymer of acrylonitrile and styrene, toughened with polybutadiene. Most electronics cases are made of this form of polystyrene, as are many sewer pipes.
Styrene can be copolymerized with other monomers; for example, divinylbenzene for cross-linking the polystyrene chains.
Polystyrene, shaped and cut with hot wire foam cutters, is used in architecture models, actual signage, amusement park and movie sets, airplane construction, and much more. Such cutters may cost just a few dollars (for a completely manual cutter) to tens of thousands of dollars for large CNC machines that can be used in high-volume industrial production.
Polysterene can also be cut with a traditional cutter, in order to do this without ruining the sides one must first dip the blade in water and cut with the blade at an angle of about 30º, the procedure has to be repeated multiple times for best results.
Some acceptable finishing materials are
Polystyrene is classified according to DIN4102 as a "B3" product, meaning highly flammable or "easily ignited". Consequently, though it is an efficient insulator at low temperatures, it is prohibited from being used in any exposed installations in building construction. It must be concealed behind drywall, sheet metal or concrete. Foamed plastic materials have been accidentally ignited and caused huge fires and losses. Examples include the Düsseldorf airport, the Channel tunnel, where it was inside a railcar and caught on fire, and the Browns Ferry nuclear plant, where fire reached through a fire retardant, reached the foamed plastic underneath, inside a firestop that did not consider bounding.
Polystyrene is used in some polymer-bonded explosives:
| Name | Explosive Ingredients | Binder Ingredients | Usage |
|---|---|---|---|
| PBX-9205 | RDX 92% | Polystyrene 6%; DOP 2% | |
| PBX-9007 | RDX 90% | Polystyrene 9.1%; DOP 0.5%; rosin 0.4% |
Plastics | Packaging materials | Household chemicals | Insulators | Organic polymers | Dielectrics | Fire
Полистирен | Polystyren | Polystyrol | Poliestireno | Polystyrène | Polystyrene | Polistirolo | Polistirols | Polystyreen | ポリスチレン | Polistyren | Isopor | Полистирол | Polystyreeni | Polystyren | 聚苯乙烯
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"Polystyrene".
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