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[[File:Expanded_polystyrene_foam_dunnage.jpg|thumb|Expanded polystyrene packaging]]
[[File:Envase de yogur.jpg|thumb|A polystyrene yogurt container]]

'''Polystyrene''' ({{pron-en|ˌpɒliˈstaɪriːn}}) ([[IUPAC]] '''Poly(1-phenylethane-1,2-diyl)'''),  abbreviated following ISO Standard '''PS''', is an [[Aromaticity|aromatic]] [[polymer]] made from the aromatic [[monomer]] [[styrene]], a liquid [[hydrocarbon]] that is commercially manufactured from [[petroleum]] by the [[chemical industry]]. Polystyrene is one of the most widely used kinds of [[plastic]].

Polystyrene is a [[thermoplastic]] substance, which is in solid (glassy) state at room temperature, but flows if heated above its [[glass transition temperature]] (for [[Molding (process)|molding]] or extrusion), and becomes solid again when cooled. Pure solid polystyrene is a colorless, hard plastic with limited flexibility. It can be cast into molds with fine detail.  Polystyrene can be [[Transparency (optics)|transparent]] or can be made to take on various colors.

Solid polystyrene is used, for example, in disposable [[cutlery]], plastic models, CD and DVD cases, and smoke detector housings. Products made from foamed polystyrene are nearly ubiquitous, for example packing materials, insulation, and foam drink cups. 

Polystyrene can be recycled, and has the number "6" as its [[resin identification code|recycling symbol]]. Polystyrene takes a very long time to [[biodegrade]]<ref>{{Cite journal|title=Studies on photocatalytic degradation of polystyrene| first= Abhijit|last= Bandyopadhyay |first2= G.|last2=Chandra Basak|year=2007|journal = Materials Science and Technology|volume = 23|issue = 3|pages=307–317 |doi=10.1179/174328407X158640}}</ref>, and is often abundant as a form of pollution in the outdoor [[environment (biophysical)|environment]], particularly along shores and waterways.

==History==
Polystyrene was discovered in 1839 by [[Eduard Simon]],<ref>[http://inventors.about.com/od/pstartinventions/a/plastics.htm The history of plastics]</ref> an [[apothecary]] in [[Berlin]]. From [[storax]], the resin of the [[Liquidambar orientalis|Turkish sweetgum tree ''(Liquidambar orientalis]]),'' he distilled an oily substance, a [[monomer]] which he named styrol. Several days later, Simon found that the styrol had thickened, presumably from oxidation, into a jelly he dubbed styrol oxide ("Styroloxyd"). 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 [[macromolecule]]s, following the thesis of German organic chemist [[Hermann Staudinger]] (1881–1965). This eventually led to the substance receiving its present name, polystyrene.

The company [[IG Farben|I. G. Farben]] began manufacturing polystyrene in [[Ludwigshafen|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.

Before 1949, the chemical engineer Fritz Stastny (1908–1985) developed pre-expanded PS beads by incorporating aliphatic hydrocarbons, such as pentane. These beads are the raw material for moulding parts or extruding sheets. BASF and Stastny applied for a patent which was issued in 1949. The moulding process was demonstrated at the Kunststoff Messe 1952 in Düsseldorf. Products were named Styropor.
 
In 1959, the [[Koppers Company]] in [[Pittsburgh, Pennsylvania]], developed expanded polystyrene (EPS) foam.{{Citation needed|date=November 2008}}

==Structure and properties==
The chemical makeup of polystyrene is a long chain hydrocarbon with every other carbon connected to a [[phenyl group]] (the name given to the aromatic ring [[benzene]], when bonded to complex carbon substituents). Polystyrene's chemical formula is (C<sub>8</sub>H<sub>8</sub>)<sub>n</sub>; it contains the [[chemical elements]] [[carbon]] and [[hydrogen]]. 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. Complete [[oxidation]] of polystyrene produces only [[carbon dioxide]] and [[water|water vapor]]. Because of its chemical inertness, polystyrene is used to fabricate containers for chemicals, solvents, and foods. 

This addition polymer of styrene results when vinyl benzene (styrene) monomers (which contain double bonds between carbon atoms) attach to form a polystyrene chain (with each carbon attached with a single bond to two other carbons and a phenyl group).

<center>[[File:Polystyrene formation.PNG]]</center>

Polystyrene is generally flexible and can come in the form of moldable solids or viscous liquids. The force of attraction in polystyrene is mainly due to short range van der Waals attractions between chains. Since the molecules and long hydrocarbon chains that consist of thousand of atoms, the total attractive force between the molecules is large.  However, when the polymer is heated (or, equivalently, deformed at a rapid rate, due to a combination of viscoelastic and thermal insulation properties), the chains are able to take on a higher degree of conformation and slide past each other. This [[intermolecular]] weakness (versus the high ''[[intramolecular]]'' strength due to the hydrocarbon backbone) allows the polystyrene chains to slide along each other, rendering the bulk system  flexible and stretchable.  The ability of the system to be readily deformed above its glass transition temperature allows polystyrene (and thermoplastic polymers in general) to be readily softened and molded with the addition of heat.

A 3-D model would show that each of the [[chirality (chemistry)|chiral]] backbone carbons lies at the center of a [[tetrahedron]], with its 4 [[chemical bond|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 is not 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 is not produced commercially.

<center>
{|align="center" class="wikitable"
|<center>[[File:Isotactic-polystyrene-chain-from-xtal-3D-balls.png|580px]]</center>
|-
|<center><small>[[Ball-and-stick model]] of part of the [[crystal structure]] of [[Tacticity#Isotactic polymers|isotactic]] polystyrene<ref>{{cite journal|doi = 10.1007/BF02731861|author = G. Natta, P. Corradini, I.W. Bassi|journal = Il Nuovo Cimento|year = 1960|volume = 15|pages = 68–82|title = Crystal structure of isotactic polystyrene}}</ref></small></center>
|}
</center>

Ordinary ''atactic'' polystyrene has these large phenyl groups [[randomness|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 a very low [[melting point]], ''T''<sub>m</sub><<''T''<sub>RT</sub>. But [[metallocene]]-[[catalysis|catalyzed]] [[polymerization]] can produce an ordered ''syndiotactic'' polystyrene with the phenyl groups on alternating sides. This form is highly crystalline with a ''T''<sub>m</sub> of {{convert|270|C|F|abbr=on}}.

Extruded polystyrene is about as strong as unalloyed [[aluminium]], but much more flexible and much lighter (1.05 g/cm<sup>3</sup> vs. 2.70 g/cm<sup>3</sup> for aluminium).

==Forms produced==
{| class="wikitable" border="1" align="right"
! colspan=2|Properties
|-
|[[Density]]
|1.05 g/cm<sup>3</sup>
|-
|[[Density]] of EPS
|16–640&nbsp;kg/m<sup>3</sup><ref name=pse1>{{cite journal|journal=New Scientist |date=June 22, 1961|url=http://books.google.com/?id=d_XOKdeyXrYC&pg=PA706|page=706|volume=240|title=Making and using an expanded plastic|author=K. Goodier}}</ref>
|-
|[[Dielectric constant]]
|2.4–2.7
|-
|[[Electrical conductivity]] (s)
|10<sup>−16</sup> [[siemens (unit)|S]]/m
|-
|[[Thermal conductivity]] (k)
|0.08 [[Thermal conductivity|W/(m·K)]]
|-
|[[Young's modulus]] (''E'')
|3000–3600 [[Pascal (unit)|MPa]]
|-
|[[Tensile strength]] (''s''<sub>t</sub>)
|46–60 MPa
|-
|Elongation at break
|3–4%
|-
|[[Charpy impact test|Notch]] test
|2–5 [[kilojoules|kJ]]/m<sup>2</sup>
|-
|[[Glass transition temperature|Glass temperature]]
|95 °C
|-
|[[Melting point]]<ref name="ILO-safety-card">[http://www.ilo.org/public/english/protection/safework/cis/products/icsc/dtasht/_icsc10/icsc1043.htm International Labour Organisation chemical safety card for polystyrene]</ref>
|240 °C
|-
|[[Vicat softening point|Vicat B]]
|90 °C<ref>A.K. van der Vegt & L.E. Govaert, Polymeren, van keten tot kunstof, ISBN 90-407-2388-5</ref>
|-
|[[Coefficient of thermal expansion|Linear expansion coefficient (a)]]
|8×10<sup>−5</sup> /[[Kelvin|K]]
|-
|[[Specific heat capacity|Specific heat]] (''c'')
|1.3 kJ/(kg·K)
|-
|[[Absorption (chemistry)|Water absorption]] (ASTM)
|0.03–0.1
|-
|[[Decomposition]]
|X years, still decaying
|-
|}

Polystyrene is commonly injection molded or extruded, while expanded polystyrene is either extruded or molded in a special process.
Polystyrene [[copolymers]] are also produced; these contain one or more other monomers in addition to styrene. In recent years the expanded polystyrene composites with cellulose<ref>{{cite journal|author=Doroudiani S, Kortschot MT|year=2004|title=Expanded Wood Fiber Polystyrene Composites: Processing-Structure-Mechanical Properties Relationships|journal=Journal of Thermoplastic Composite Materials|volume=17|pages=13–30|doi=10.1177/0892705704035405}}</ref><ref>{{cite journal|doi=10.1002/polb.10129|title=Sorption and diffusion of carbon dioxide in wood-fiber/polystyrene composites|year=2002|last1=Doroudiani|first1=Saeed|last2=Chaffey|first2=Charles E.|last3=Kortschot|first3=Mark T.|journal=Journal of Polymer Science Part B: Polymer Physics|volume=40|pages=723}}</ref> and starch<ref>{{cite journal|doi=10.1177/0021955X07076532|title=Foaming of Polystyrene/ Thermoplastic Starch Blends|year=2007|last1=Mihai|first1=M.|last2=Huneault|first2=M. A.|last3=Favis|first3=B. D.|journal=Journal of Cellular Plastics|volume=43|pages=215}}</ref> have also been produced.

Extruded closed-cell polystyrene foam is sold under the [[trademark]] [[Styrofoam]] by [[Dow Chemical Company|Dow Chemical]]. This term is often used informally for other foamed polystyrene products.

Polystyrene is used in some [[polymer-bonded explosive]]s:

{| class="wikitable" border="1"
|+ Polystyrene PBX examples
|-
! Name !! Explosive ingredients !! Binder ingredients
|-
| PBX-9205 || [[RDX]] 92% || Polystyrene 6%; [[DEHP|DOP]] 2%
|-
| PBX-9007 || RDX 90% || Polystyrene 9.1%; DOP 0.5%; resin 0.4%
|}

It is also a component of [[napalm]]<ref name="GS Napalm">[http://www.globalsecurity.org/military/systems/munitions/napalm.htm Napalm]</ref> and a component of most designs of [[Teller-Ulam design|hydrogen bombs]]{{Citation needed|date=November 2008}}.

===Sheet or molded polystyrene===
[[File:Caja de CD.jpg|thumb|CD case made from General Purpose Polystyrene (GPPS) and High Impact Polystyrene (HIPS)]]
[[File:Maquinilla de afeitar desechable.JPG|thumb|Disposable polystyrene razor]]
Polystyrene (PS) is economical, and is used for producing [[plastic model]] assembly kits, plastic cutlery, [[CD and DVD packaging|CD "jewel" cases]], [[smoke detector]] housings, [[license plate]] frames, and many other objects where a fairly rigid, economical plastic is desired. Production methods include [[thermoforming]] and [[injection molding]].

Polystyrene [[Petri dish]]es and other [[laboratory]] containers such as [[test tubes]] and [[microplate]]s play an important role in biomedical research and science. For these uses, articles are almost always made by [[injection molding]], and often sterilized post-molding, either by irradiation or treatment with [[ethylene oxide]]. Post-mold surface modification, usually with [[oxygen]]-rich [[Plasma (physics)|plasma]]s, is often done to introduce polar groups. Much of modern biomedical research relies on the use of such products; they therefore play a critical role in pharmaceutical research.<ref>{{cite web|author=Jed Norton|title=Blue Foam, Pink Foam and Foam Board|publisher=Antenociti's Workshop|url=http://www.barrule.com/workshop/images/info/foams/index.htm|accessdate=2008-01-29}}</ref>

===Foams===
Polystyrene foams are good thermal insulators and are therefore often used as building insulation materials, such as in structural insulated panel building systems. They are also used for non-weight-bearing architectural structures (such as ornamental [[column|pillars]]).
PS foams exhibit also good damping properties, therefore it is used widely in packaging. 

====Expanded polystyrene====
Expanded polystyrene (EPS) is a rigid and tough, closed-cell foam. It is usually white and made of pre-expanded polystyrene beads. Familiar uses include molded sheets for building insulation and packing material ([[Foam peanut|"peanuts"]]) for cushioning fragile items inside boxes. Sheets are commonly packaged as [[rigid panel]]s (size 4 by 8 or 2 by 8 feet in the United States), which are also known as "bead-board". [[Thermal resistivity]] is usually about 28 m·[[Kelvin|K]]/[[Watt|W]] (or R-4 per inch in American customary units). Some EPS boards have a [[flame spread]] of less than 25 and a [[smoke-developed index]] of less than 450, which means they can be used without a fire barrier (but require a 15 minute thermal barrier) according to [[Building code#United States|US building codes]]. A growing use of EPS in construction is [[Insulating concrete forms]].
The density range is about 16–640&nbsp;kg/m<sup>3</sup>.<ref name=pse1/> The most common processing method is thermal cutting with hot wires.<ref>''[http://www.ceresana.com/en/insight/products/plastics/expandable-polystyrene/ Expandable Polystyrene]'', Insight database from Ceresana Research</ref>

====Extruded polystyrene foam====
Extruded polystyrene foam (XPS) consists of closed cells, offers improved surface roughness as higher stiffness and reduced thermal conductivity. The density range is about 28 – 45&nbsp;kg/m<sup>3</sup>.

Extruded polystyrene material is also used in [[craft]]s and [[model (physical)|model]] building, particularly [[Architecture|architectural]] models. Because of the extrusion manufacturing process, XPS does not require facers to maintain its thermal or physical property performance. Thus, it makes a more uniform substitute for [[corrugated cardboard]]. Thermal resistivity is usually about 35 m·K/W (or R-5 per inch in American customary units). 

[[Styrofoam]] is a trademarked name for XPS; however, it is often also used in the [[United States]] as a generic name for all polystyrene foams.

===Copolymers===
Pure polystyrene is [[toughness|brittle]], but [[hardness|hard]] enough that a fairly high-performance product can be made by giving it some of the properties of a stretchier material, such as [[polybutadiene]] rubber. The two such materials can never normally be mixed because of the amplified effect of [[Polymer#Intermolecular forces|intermolecular forces]] on polymer [[insolubility]] (see [[plastic recycling]]), but if polybutadiene is added during polymerization it can become chemically bonded to the polystyrene, forming a [[graft copolymer]] which helps to incorporate normal polybutadiene into the final mix, resulting in '''high-impact polystyrene''' or '''HIPS''', often called "high-impact plastic" in advertisements. One commercial name for HIPS is Bextrene. Common applications of HIPS include toys and product casings. HIPS is usually [[Injection molding|injection molded]] in production. Autoclaving polystyrene can compress and harden the material.

Several other copolymers are also used with styrene. [[Acrylonitrile butadiene styrene]] or ABS plastic is similar to HIPS: a copolymer of '''a'''crylonitrile and '''s'''tyrene, toughened with poly'''b'''utadiene. Most electronics cases are made of this form of polystyrene, as are many sewer pipes. [[Styrene-acrylonitrile resin|SAN]] is a copolymer of styrene with [[acrylonitrile]], and [[styrene maleic anhydride|SMA]] one with [[maleic anhydride]]. Styrene can be copolymerized with other monomers; for example, [[divinylbenzene]] for cross-linking the polystyrene chains.

===Oriented polystyrene===
Oriented polystyrene (OPS) is produced by stretching extruded PS film, improving stiffness.

==Disposal and environmental issues==
Polystyrene is not easily [[recyclable|recycled]] because of its light weight (especially if foamed) and its low scrap value. It is generally not accepted in [[kerbside collection|kerbside (curbside) collection]] recycling programs. In Germany, however, polystyrene is collected, as a consequence of the packaging law (Verpackungsverordnung) that requires manufacturers to take responsibility for recycling or disposing of any packaging material they sell.

===Environmental impact===
Discarded polystyrene does not [[biodegrade]] for hundreds of years and is resistant to [[photolysis]].<ref>{{Cite journal|title=Studies on photocatalytic degradation of polystyrene| first= Abhijit|last= Bandyopadhyay |first2= G.|last2=Chandra Basak|year=2007|journal = Materials Science and Technology|volume = 23|issue = 3|pages=307–317 |doi=10.1179/174328407X158640}}</ref>  Because of this, very little of the waste discarded in today's modern, highly engineered landfills biodegrades. Because degradation of materials creates potentially harmful liquid and gaseous by-products that could contaminate groundwater and air, today's landfills are designed to minimize contact with air and water required for degradation, thereby practically eliminating the degradation of waste.<ref>{{cite book|title=Rubbish! The Archeology of Garbage|author= William Rathje and Cullen Murphy|year=1989}}</ref>

Polystyrene foam is a major component of plastic debris in the ocean, where it becomes toxic to marine life. Foamed polystyrene blows in the wind and floats on water, and is abundant in the outdoor environment. Weathering by wind, sun, rain, and wave action degrade polystyrene to known and suspected carcinogens, including styrene monomer (SM), styrene dimer (SD) and styrene trimer (ST). <ref>http://www.sciencedaily.com/releases/2009/08/090819234651.htm</ref> <ref>Barry, Carolyn. "Plastic Breaks Down In Ocean, After All- And Fast." National Geographic 20 Aug. 2009:</ref><ref>[http://www.independent.co.uk/news/science/scientists-uncover-new-ocean-threat-from-plastics-1774337.html Scientists uncover new ocean threat from plastics], The Independent, 20 August 2009.</ref> However, styrene is an organic, naturally occurring substance in our environment and to date, no regulatory body anywhere in the world has classified styrene as a known human [[carcinogen]], although several refer to it in various contexts as a possible or potential human carcinogen.<ref>International Agency for Research on Cancer (IARC) [http://monographs.iarc.fr/ENG/Classification/crthgr02a.php "Styrene is probably carcinogenic to humans. Group 2A"], "IARC Monographs, Classifications", 1994<!--Accessed January 2010--></ref> Furthermore, styrene is quickly broken down in the air, evaporates quickly in shallow soil and water, and what remains in soil and water can be further broken down by bacteria and microorganisms.<ref>[http://www.atsdr.cdc.gov/tfacts53.pdf Styrene Fact Sheet]</ref><ref>{{cite book|author=Denis H. James William M. Castor|chapter=Styrene|title=Ullmann’s Encyclopedia of Industrial Chemistry|publisher=Wiley-VCH|year=2005}}</ref>

Polystyrene foams are produced using blowing agents that form bubbles and expand the foam. In expanded polystyrene, these are usually [[hydrocarbon]]s such as [[pentane]], which may pose a flammability hazard in manufacturing or storage of newly manufactured material, but have relatively mild environmental impact. However, extruded polystyrene is usually made with [[hydrochlorofluorocarbon]]s (HCFC) blowing agents which have effects on ozone depletion and on global warming. Their ozone depletion potential is greatly reduced relative to [[chlorofluorocarbon]] (CFC) which were formerly used, but their [[global warming potential]] can be on the order of 1000 or more, meaning it has 1000 times greater effect on global warming than does carbon dioxide.<ref>[http://www.grida.no/publications/other/ipcc_tar/?src=/climate/ipcc_tar/wg1/248.htm IPCC Third Assessment Report, Climate Change 2001]:
Working Group I: The Scientific Basis. Section 6.12.2 Direct GWPs.</ref>

That being said, global warming regulations should have minimal direct impact on the PS industry. There are few greenhouse gas emissions generated by the PS industry in comparison to other industries such as oil refineries and automobiles.<ref>[http://www.americanchemistry.com/s_plastics/doc_pfpg.asp?CID=1417&DID=5332#19 Polystyrene (PS) Frequently Asked Questions], American Chemistry Council</ref>

Regardless, on September 21, 2007, approximately 200 countries agreed to accelerate the elimination of hydrochlorofluorocarbons entirely by 2020 in a United Nations-sponsored Montreal summit. Developing nations were given until 2030.<ref>[http://www.epa.gov/ozone/title6/phaseout/hcfc.html HCFC Phaseout Schedule], US EPA</ref> Ultimately, hydrofluorocarbons (HFCs) will replace HCFCs with essentially no ozone destruction.

While there is less concern about the health effects of EPS itself, the [[brominated flame retardants]] used in most EPS foam (decaBDE or [[hexabromocyclododecane]] are the most commonly used) could possibly create health and environmental risks that are generating some concern with the EPA.<ref>[http://www.epa.gov/hpvis/rbp/HBCD.3194556.Web.RBP.31308.pdf EPA information on HBCD]</ref>

Since the early 1990s, [[Foam_peanut#Starch-based_packing_peanuts|starch-based foam packing peanuts]] have been used as a replacement for PS packing peanuts.  Foamed [[polylactic acid]] (PLA), marketed as Biofoam<ref>[http://www.biofoam.nl/uploads/Press%20release%20BioFoam%20C2C%202009-12.pdf BioFoam® Synbra Group]</ref>, has also been developed.

In 2007, Eben Bayer, a student at [[Rensselaer Polytechnic Institute]], invented<ref>Shin, L. (2009). [http://greeninc.blogs.nytimes.com/2009/04/13/using-fungi-to-replace-styrofoam/ Using Fungi to Replace Styrofoam]. ''NY Times''.</ref> an environmentally-friendly replacement for polystyrene packaging using the mineral [[perlite]] bonded with lignin-containing agricultural waste, degraded by fungi, which he calls Ecocradle.<ref>[http://www.ecovativedesign.com/ecocradle Evocative Designs LLC, Ecocradle]</ref>

===Recycling===
[[File:Resin-identification-code-6-PS.svg|thumb|90px|The [[resin identification code]] symbol for polystyrene<!--The [[Unicode]] character is U+2678, which will appear here if you have a suitable font installed: <font size="6">♸</font>.-->]]

Currently, the majority of polystyrene products are not recycled. Expanded polystyrene scrap can be easily added to products such as EPS insulation sheets and other EPS materials for construction applications. Commonly, manufacturers cannot obtain sufficient scrap because of the aforementioned collection issues. When it is not used to make more EPS, foam scrap can be turned into clothes hangers, park benches, flower pots, toys, rulers, stapler bodies, seedling containers, picture frames, and architectural molding from recycled PS.<ref>[http://pspc.intoweb.co.za/index.php?page=recycle1 Polystyrene recycling.] Polystyrene packaging council. Retrieved on 2009-03-06.</ref>

Recycled EPS is also used in many metal casting operations. [[Rastra]] is made from EPS that is combined with cement to be used as an insulating amendment in the making of concrete foundations. American manufacturers have produced [[insulated concrete forms]] made with approximately 80% recycled EPS since 1993. However, polystyrene recycling is not a closed loop, producing more polystyrene; polystyrene cups and other packaging materials are instead usually used as fillers in other plastics, or in other items that cannot themselves be recycled and are thrown away.{{Citation needed|date=March 2009}}

===Incineration===
If polystyrene is properly incinerated at high temperatures, the only chemicals generated are water, carbon dioxide, some volatile compounds, and carbon soot.<ref name=burning>[http://www.newton.dep.anl.gov/askasci/chem00/chem00053.htm Polystyrene Foam Burning Danger]</ref> According to the [[American Chemistry Council]], when polystyrene is incinerated in modern facilities, the final volume is 1% of the starting volume; most of the polystyrene is converted into carbon dioxide, water vapor, and heat. Because of the amount of heat released, it is sometimes used as a power source for [[steam]] or [[electricity generation]].<ref>{{Cite news|title = Ease of Disposal|url = http://www.americanchemistry.com/s_plastics/sec_pfpg.asp?CID=1434&did=5226|accessdate = 2009-06-25}}</ref>

When polystyrene was burned at temperatures of 800-900 °C (the typical range of a modern incinerator), the products of combustion consisted of "a complex mixture of polycyclic aromatic hydrocarbons (PAHs) from alkyl benzenes to benzo[ghi]perylene. Over 90 different compounds were identified in combustion effluents from polystyrene."<ref>{{cite journal|url=http://www.ejnet.org/plastics/polystyrene/disposal.html|author=Hawley-Fedder, R.A.; Parsons, M.L. and Karasek, F.W.|journal=Products Obtained During Combustion of Polymers Under Simulated Incinerator Conditions, II Polystyrene|doi=10.1016/S0021-9673(01)90737-X|title=Products obtained during combustion of polymers under simulated incinerator conditions II. Polystyrene|year=1984|volume=315|pages=201}}</ref>

When burned without enough oxygen or at lower temperatures (as in a campfire or a household fireplace), polystyrene can produce [[polycyclic aromatic hydrocarbon]]s, [[carbon black]], and [[carbon monoxide]], as well as styrene monomers.<ref name=burning /><ref>[http://www.newton.dep.anl.gov/askasci/chem00/chem00532.htm Burning Polystyrene Foam]</ref>

===Burial===
Foam cups and other polystyrene products can be safely buried in [[landfill]]s, since it is as stable as [[concrete]] or [[brick]]. No plastic film is required to protect the air and underground water. 

===Reducing===
Some effort is being made to find alternatives to polystyrene foam, especially in restaurant settings. Restricting the use of foamed polystyrene takeout food packaging is a priority of many solid waste [[environmental organization]]s. However, the Plastics Foodservice Packaging Group counters that in US, less than 1% by weight of solid waste disposed is polystyrene. A campaign to achieve the first ban of polystyrene foam from the food & beverage industry in [[Canada]] was launched in [[Toronto]] as of January 2007, by local non-profit organization [[NaturoPack]].<ref>[http://naturopack.org/getittogogreenmain.html Naturopack Campaign Page]</ref>. Portland, Ore., and San Francisco are among about one hundred cities in the United States that currently have some sort of ban on polystyrene foam in restaurants. For instance, in 2007 restaurants in Oakland, California were required to switch to disposable food containers that will biodegrade if added to food compost.<ref>Hadish, Cindy. "Food for thought: 100 U.S. cities enact bans." Gazette, The (Cedar Rapids, IA) 2 Apr. 2008.</ref>

Although polystyrene can be recycled at recycling facilities, most polystyrene is not recycled. The EPA ([[United States Environmental Protection Agency]]) estimates that 25 billion polystyrene cups are tossed every year. Since polystyrene degrades very slowly- more than 500 years for a single cup- the EPA considers this a serious environmental problem.  Several green leaders, from the Dutch Ministry of the Environment to Starbucks' Green Team, advise that individuals reduce their environmental impact by using reusable coffee cups.<ref>{{cite news|author=Dineen, Shauna|title=The Throwaway Generation: 25 Billion Styrofoam Cups a Year|publisher=E-The Environmental Magazine|date=Nov. - Dec. 2005|url=http://www.emagazine.com/view/?2933}}</ref>

==Finishing==
In the United States, environmental protection regulations prohibit the use of solvents on polystyrene (which would dissolve the polystyrene and de-foam most foams anyway).{{Citation needed|date=April 2010}}

Some acceptable finishing materials are
*Water-based [[paint]] ([[artist]]s have created [[painting]]s on polystyrene with [[gouache]]){{Citation needed|date=April 2010}}
*[[Mortar (masonry)|Mortar]] or acrylic/cement render, often used in the building industry as a weather-hard overcoat that hides the foam completely after finishing the objects.{{Citation needed|date=April 2010}}
*Cotton wool or other fabrics used in conjunction with a stapling implement.{{Citation needed|date=April 2010}}

==Health and fire hazards==

There has been concern about the trace presence of polystyrene's production chemicals in the final plastic product, most of which are toxic if not removed. For instance [[benzene]], which is used to produce [[ethylbenzene]] for styrene, is a known carcinogen. As well, unpolymerized styrene may pose health risks. 

However,

{{quote|Based on scientific tests over five decades, government safety agencies have determined that polystyrene is safe for use in foodservice products. For example, polystyrene meets the stringent standards of the U.S. Food and Drug Administration and the European Commission/European Food Safety Authority for use in packaging to store and serve food. The Hong Kong Food and Environmental Hygiene Department recently reviewed the safety of serving various foods in polystyrene foodservice products and reached the same conclusion as the U.S. FDA.<ref>[http://www.americanchemistry.com/s_plastics/doc_pfpg.asp?CID=2300&DID=10005#ps_1 Q & A on the Safety of Polystyrene Foodservice Products]</ref>}}

and from 1999 to 2002, a comprehensive review of the potential health risks associated with exposure to styrene was conducted by a 12 member international expert panel selected by the Harvard Center for Risk Assessment. The scientists had expertise in toxicology, epidemiology, medicine, risk analysis, pharmacokinetics, and exposure assessment.

{{quote|The Harvard study reported that styrene is naturally present in foods such as strawberries, beef, and spices, and is naturally produced in the processing of foods such as wine and cheese. The study also reviewed all the published data on the quantity of styrene contributing to the diet due to migration of food packaging and disposable food contact articles, and concluded there is no cause for concern for the general public from exposure to styrene from foods or styrenic materials used in food-contact applications, such as polystyrene packaging and food service containers.<ref>{{cite journal|doi=10.1080/10937400252972162|title=A comprehensive evaluation of the potential health risks associated with occupational and environmental exposure to styrene|year=2002|last1=Cohen|first1=Joshua T.|last2=Carlson|first2=Gary|last3=Charnley|first3=Gail|last4=Coggon|first4=David|last5=Delzell|first5=Elizabeth|last6=Graham|first6=John D.|last7=Greim|first7=Helmut|last8=Krewski|first8=Daniel|last9=Medinsky|first9=Michele|journal=Journal of Toxicology and Environmental Health Part B: Critical Reviews|volume=5|pages=1}}</ref>}}

The LD<sub>50</sub> of styrene is 3&nbsp;mmol/kg as determined by the Registry of Cytotoxicity Data (ZEBET) 7.1, National Institute of Health, Berlin, Germany. 

There are, of course, studies concerning polystyrene containers used for food packaging which find that styrene oligomers migrate into the food.<ref>{{cite journal|author=Sakamato H, Matsuzawa A, Itoh R, Tohyama Y|year=2000|title=Quantitative Analysis of Styrene Dimer and Trimers Migrated from Disposable Lunch Boxes|journal=J Food Hyg Soc Japan|volume=41|pages=200–205|url=http://sciencelinks.jp/j-east/article/200016/000020001600A0689499.php|doi=10.3358/shokueishi.41.200}}</ref>. For instance, one Japanese study conducted on wild-type and AhR-null mice found that the styrene trimer, which the authors detected in cooked polystyrene container-packed instant foods, may increase thyroid hormone levels.<ref>{{cite journal|author=Yanagiba, Yukie ''et al.''|title=Styrene Trimer May Increase Thyroid Hormone Levels via Down-Regulation of the Aryl Hydrocarbon Receptor (AhR) Target Gene UDP-Glucuronosyltransferase|journal=Environmental Health Perspectives|volume=116|year=2008|pages=740–745|url=http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2430229/|format=free text|pmid=18560529|doi=10.1289/ehp.10724|issue=6|pmc=2430229}}</ref>

Polystyrene is classified according to DIN4102 as a "B3" product, meaning highly flammable or "easily ignited." Consequently, although it is an efficient insulator at low temperatures, its use is prohibited in any exposed installations in [[building construction]] if the material is not [[flame retardant]], e.g., with [[hexabromocyclododecane]]. It must be concealed behind [[drywall]], sheet metal or [[concrete]]. Foamed polystyrene plastic materials have been accidentally ignited and caused huge fires and losses, for example at the [[Düsseldorf International Airport]], the [[Channel tunnel]] (where polystyrene was inside a railcar that caught fire), and the [[Browns Ferry Nuclear Power Plant]] (where fire breached a fire retardant and reached the foamed plastic underneath, inside a [[firestop]] that had not been tested and certified in accordance with the final installation).

In addition to fire hazard, polystyrene can be dissolved by substances that contain [[acetone]] (such as most [[Aerosol spray|aerosol paint spray]]s), and by [[cyanoacrylate]] glues.

==See also==
{{colbegin|3}}
*[[Bioplastic]]
*[[Insulating concrete forms]]
*[[Geofoam]]
*[[Structural insulated panel]]
*[[Styrofoam]]
{{colend}}

==References==
{{reflist|2}}

==External links==
{{commons|Polystyrene|Polystyrene}}
*[http://www.pslc.ws/mactest/styrene.htm Polystyrene] - The University of Southern Mississippi
*[http://www.plasticsindustry.org/AboutPlastics/content.cfm?ItemNumber=825&navItemNumber=1124 SPI resin identification code] - Society of the Plastics Industry
*[http://www.sciam.com/article.cfm?chanID=sa003&articleID=0007B0AE-88AF-13FF-88AF83414B7F0000 Bacteria Turns Styrofoam into Biodegradable Plastic] - Scientific American, February 27, 2006
*[http://www.polystyrene.org/polystyrene_facts/facts.html Polystyrene (packaging) facts]
Plastics Foodservice Packaging Group (PFPG) of the American Chemistry Council 

{{HealthIssuesOfPlastics}}
{{Plastics}}

[[Category:Insulators]]
[[Category:Building insulation materials]]
[[Category:Organic polymers]]
[[Category:Packaging materials]]

[[Category:Thermoplastics]]

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