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Polycarbonates (PC) are a group of
thermoplastic A thermoplastic, or thermosoftening plastic, is a plastic polymer material that becomes pliable or moldable at a certain elevated temperature and solidifies upon cooling. Most thermoplastics have a high molecular mass, molecular weight. The polyme ...
polymers containing s in their chemical structures. Polycarbonates used in engineering are strong, tough materials, and some grades are optically transparent. They are easily worked, , and thermoformed. Because of these properties, polycarbonates find many applications. Polycarbonates do not have a unique resin identification code (RIC) and are identified as "Other", 7 on the RIC list. Products made from polycarbonate can contain the precursor monomer
bisphenol A Bisphenol A (BPA) is an organic compound#Synthetic compounds, organic synthetic compound with the chemical formula (CH3)2C(C6H4OH)2 belonging to the group of diphenylmethane derivatives and bisphenols, with two hydroxyphenyl Functional group, gro ...

(BPA).

# Structure

Carbonate esters have planar OC(OC)2 cores, which confers rigidity. The unique O=C bond is short (1.173 Å in the depicted example), while the C-O bonds are more ether-like (the bond distances of 1.326 Å for the example depicted). Polycarbonates received their name because they are
polymers A polymer (; Greek '' poly-'', "many" + '' -mer'', "part") is a substance or material consisting of very large molecule File:Pentacene on Ni(111) STM.jpg, A scanning tunneling microscopy image of pentacene molecules, which consist of line ...
containing s (−O−(C=O)−O−). A balance of useful features, including temperature resistance, impact resistance and optical properties, positions polycarbonates between commodity plastics and engineering plastics.

# Production

The main polycarbonate material is produced by the reaction of
bisphenol A Bisphenol A (BPA) is an organic compound#Synthetic compounds, organic synthetic compound with the chemical formula (CH3)2C(C6H4OH)2 belonging to the group of diphenylmethane derivatives and bisphenols, with two hydroxyphenyl Functional group, gro ...

(BPA) and phosgene . The overall reaction can be written as follows: The first step of the synthesis involves treatment of bisphenol A with sodium hydroxide, which deprotonates the hydroxyl groups of the bisphenol A.Volker Serini "Polycarbonates" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2000. :(HOC6H4)2CMe2 + 2 NaOH → Na2(OC6H4)2CMe2 + 2 H2O The diphenoxide (Na2(OC6H4)2CMe2) reacts with phosgene to give a chloroformate, which subsequently is attacked by another phenoxide. The net reaction from the diphenoxide is: :Na2(OC6H4)2CMe2 + COCl2 → 1/n [OC(OC6H4)2CMe2]n + 2 NaCl In this way, approximately one billion kilograms of polycarbonate is produced annually. Many other diols have been tested in place of bisphenol A, e.g. 1,1-bis(4-hydroxyphenyl)cyclohexane and dihydroxybenzophenone. The cyclohexane is used as a comonomer to suppress crystallisation tendency of the BPA-derived product. Tetrabromobisphenol A is used to enhance fire resistance. Tetramethylcyclobutanediol has been developed as a replacement for BPA. An alternative route to polycarbonates entails transesterification from BPA and diphenyl carbonate: :(HOC6H4)2CMe2 + (C6H5O)2CO → 1/n [OC(OC6H4)2CMe2]n + 2 C6H5OH The diphenyl carbonate was derived in part from carbon monoxide, this route being greener than the phosgene method.

# Properties and processing

Polycarbonate is a durable material. Although it has high impact-resistance, it has low scratch-resistance. Therefore, a hard coating is applied to polycarbonate eyewear corrective lens, lenses and polycarbonate exterior automotive components. The characteristics of polycarbonate compare to those of polymethyl methacrylate (PMMA, acrylic), but polycarbonate is stronger and will hold up longer to extreme temperature. Thermally processed material is usually totally amorphous, and as a result is highly Transparency (optics), transparent to visible light, with better light transmission than many kinds of glass. Polycarbonate has a glass transition temperature of about , so it softens gradually above this point and flows above about . Tools must be held at high temperatures, generally above to make strain-free and stress-free products. Low molecular mass grades are easier to mold than higher grades, but their strength is lower as a result. The toughest grades have the highest molecular mass, but are more difficult to process. Unlike most thermoplastics, polycarbonate can undergo large plastic deformations without cracking or breaking. As a result, it can be processed and formed at room temperature using sheet metal techniques, such as bending on a Brake (sheet metal bending), brake. Even for sharp angle bends with a tight radius, heating may not be necessary. This makes it valuable in prototyping applications where transparent or electrically non-conductive parts are needed, which cannot be made from sheet metal. Poly(methyl methacrylate), PMMA/Acrylic, which is similar in appearance to polycarbonate, is brittle and cannot be bent at room temperature. Main transformation techniques for polycarbonate resins: *extrusion into tubes, rods and other profiles including multiwall *extrusion with cylinders (calenders) into sheets () and films (below ), which can be used directly or manufactured into other shapes using thermoforming or secondary Manufacturing, fabrication techniques, such as bending, drilling, or routing. Due to its chemical properties it is not conducive to laser-cutting. *injection molding into ready articles Polycarbonate may become Brittleness, brittle when exposed to ionizing radiation above

# Applications

## Electronic components

Polycarbonate is mainly used for electronic applications that capitalize on its collective safety features. Being a good electrical insulator and having heat-resistant and flame-retardant properties, it is used in various products associated with electrical and telecommunications hardware. It can also serve as a dielectric in high-stability capacitors. However
commercial manufacture
of polycarbonate capacitors mostly stopped after sole manufacturer Bayer AG stopped making capacitor-grade polycarbonate film at the end of year 2000.

## Construction materials

The second largest consumer of polycarbonates is the construction industry, e.g. for domelights, flat or curved glazing, roofing sheets and sound walls.

## Data storage

A major polycarbonate market is the production of compact discs, DVDs, and Blu-ray discs. These discs are produced by injection-molding polycarbonate into a mold cavity that has on one side a metal stamper containing a negative image of the disc data, while the other mold side is a mirrored surface. Typical products of sheet/film production include applications in advertisement (signs, displays, poster protection).

## Automotive, aircraft, and security components

In the automotive industry, injection-molded polycarbonate can produce very smooth surfaces that make it well-suited for sputter deposition or Evaporation (deposition), evaporation deposition of aluminium without the need for a base-coat. Decorative bezels and optical reflectors are commonly made of polycarbonate. Due to its low weight and high impact resistance, polycarbonate is the dominant material for making automotive headlamp lenses. However, automotive headlamps require outer surface coatings because of its low scratch resistance and susceptibility to ultraviolet degradation (yellowing). The use of polycarbonate in automotive applications is limited to low stress applications. Stress from fasteners, plastic welding and molding render polycarbonate susceptible to stress corrosion cracking when it comes in contact with certain accelerants such as salt water and plastisol. It can be laminated to make bullet-proof glass, bullet-proof "glass", although "bullet-resistant" is more accurate for the thinner windows, such as are used in bullet-resistant windows in automobiles. The thicker barriers of transparent plastic used in teller's windows and barriers in banks are also polycarbonate. So-called "theft-proof" large plastic packaging for smaller items, which cannot be opened by hand, is typically made from polycarbonate. The cockpit canopy of the Lockheed Martin F-22 Raptor jet fighter is made from a piece of high optical quality polycarbonate, and is the largest piece of its type formed in the world.

## Niche applications

polycarbonate sheet
may have the anti-UV layer added as a special coating or a Plastics extrusion#Coextrusion, coextrusion for enhanced weathering resistance. Polycarbonate is also used as a printing substrate for nameplate and other forms of industrial grade under printed products. The polycarbonate provides a barrier to wear, the elements, and fading.

### Medical applications

Many polycarbonate grades are used in medical applications and comply with both ISO 10993-1 and USP Class VI standards (occasionally referred to as PC-ISO). Class VI is the most stringent of the six USP ratings. These grades can be sterilized using steam at 120 °C, gamma radiation, or by the ethylene oxide (EtO) method. Dow Chemical strictly limits all its plastics with regard to medical applications. Aliphatic polycarbonates have been developed with improved biocompatibility and degradability for nanomedicine applications.

## Mobile phones

Some major smartphone manufacturers use polycarbonate. Nokia used polycarbonate in their phones starting with the Nokia N9, N9's unibody case in 2011. This practice continued with various phones in the Lumia series. Samsung has started using polycarbonate with Samsung Galaxy S III, Galaxy S III's ''hyperglaze''-branded removable battery cover in 2012. This practice continues with various phones in the Samsung Galaxy, Galaxy series. Apple started using polycarbonate with the iPhone 5C's unibody case in 2013. Benefits over glass and metal back covers include durability against shattering (weakness of glass), bending and scratching (weakness of metal), shock absorption, low manufacturing costs, and no interference with radio signals and wireless charging (weakness of metal). Polycarbonate back covers are available in glossy or matte surface textures.

# History

Polycarbonates were first discovered in 1898 by Alfred Einhorn, a German scientist working at the University of Munich. However, after 30 years of laboratory research, this class of materials was abandoned without commercialization. Research resumed in 1953, when Hermann Schnell at Bayer in Uerdingen, Germany patented the first linear polycarbonate. The brand name "Makrolon" was registered in 1955. Also in 1953, and one week after the invention at Bayer, Daniel Fox (chemist), Daniel Fox at General Electric in Schenectady, New York, independently synthesized a Branching (polymer chemistry), branched polycarbonate. Both companies filed for U.S. patents in 1955, and agreed that the company lacking priority would be granted a license to the technology. Patent priority was resolved in Bayer's favor, and Bayer began commercial production under the trade name Makrolon in 1958. GE began production under the name Lexan in 1960, creating the SABIC, GE Plastics division in 1973. After 1970, the original brownish polycarbonate tint was improved to "glass-clear."

# Potential hazards in food contact applications

The use of polycarbonate containers for the purpose of food storage is controversial. The basis of this controversy is their hydrolysis (degradation by water, often referred to as leaching) occurring at high temperature, releases
bisphenol A Bisphenol A (BPA) is an organic compound#Synthetic compounds, organic synthetic compound with the chemical formula (CH3)2C(C6H4OH)2 belonging to the group of diphenylmethane derivatives and bisphenols, with two hydroxyphenyl Functional group, gro ...

: :1/n [OC(OC6H4)2CMe2]n + H2O → (HOC6H4)2CMe2 + CO2 More than 100 studies have explored the bioactivity of bisphenol A derived from polycarbonates. Bisphenol A appeared to be released from polycarbonate animal cages into water at room temperature and it may have been responsible for enlargement of the reproductive organs of female mice. However, the animal cages used in the research were fabricated from industrial grade polycarbonate, rather than FDA food grade polycarbonate. An analysis of the literature on bisphenol A leachate low-dose effects by vom Saal and Hughes published in August 2005 seems to have found a suggestive correlation between the source of funding and the conclusion drawn. Industry-funded studies tend to find no significant effects whereas government-funded studies tend to find significant effects. Sodium hypochlorite bleach and other alkali cleaners catalyze the release of the bisphenol A from polycarbonate containers. Polycarbonate is incompatible with ammonia and acetone. Alcohol is a recommended organic solvent for cleaning grease and oils from polycarbonate.

# Environmental impact

## Disposal

Studies have shown that at temperatures above 70 °C, and high humidity, polycarbonate will hydrolyze to Bisphenol A, Bis-phenol A (BPA). This condition is similar to that observed in most incinerators. After about 30 days at 85 °C / 96% RH, surface crystals are formed which for 70% consisted of BPA. BPA is a compound that is currently on the list of potential environmental hazardous chemicals. It is on the watch list of many countries, such as United States and Germany. -(-OC6H4)2C(CH3)2CO-)-n + H2O $\longrightarrow$ (CH3)2C(C6H4OH)2 + CO2 The leaching of BPA from polycarbonate can also occur at environmental temperature and normal pH (in landfills).The amount of leaching increases as the discs get older. A study found that the decomposition of BPA in landfills (under anaerobic conditions) will not occur. It will therefore be persistent in landfills. Eventually, it will find its way into water bodies and contribute to aquatic pollution.

## Photo-oxidation of polycarbonate

In the presence of UV light, oxidation of this polymer yields compounds such as ketones, phenols, o-phenoxybenzoic acid, benzyl alcohol and other unsaturated compounds. This has been suggested through kinetic and spectral studies. The yellow color formed after long exposure to sun can also be related to further oxidation of phenolic end group (OC6H4)2C(CH3)2CO )n + O2 , R* → (OC6H4)2C(CH3CH2)CO)n This product can be further oxidized to form smaller unsaturated compounds. This can proceed via two different pathways, the products formed depends on which mechanism takes place. Pathway A (OC6H4)2C(CH3CH2)CO + O2, H* $\longrightarrow$ HO(OC6H4)OCO + CH3COCH2(OC6H4)OCO Pathway B (OC6H4)2C(CH3CH2)CO)n + O2, H* $\longrightarrow$ OCO(OC6H4)CH2OH + OCO(OC6H4)COCH3 Photo-oxidation reaction.

## Photo-aging reaction

Photo-aging is another degradation route for polycarbonates. Polycarbonate molecules (such as the aromatic ring) absorb UV radiation. This absorbed energy causes cleavage of covalent bonds which initiates the photo-aging process. The reaction can be propagated via side chain oxidation, ring oxidation or Fries rearrangement#Photo-Fries rearrangement, photo-Fries rearrangement. Products formed include phenyl salicylate, dihydroxybenzophenone groups, and hydroxydiphenyl ether groups. n(C16H14O3) $\longrightarrow$ C16H17O3 + C13H10O3 Polycarbonate Phenyl salicylate 2,2-dihydroxybenzophenone

Waste polycarbonate will degrade at high temperatures to form solid, liquid and gaseous pollutants. A study showed that the products were about 40–50 wt.% liquid, 14–16 wt.% gases, while 34–43 wt.% remained as solid residue. Liquid products contained mainly phenol derivatives (∼75wt.%) and bisphenol (∼10wt.%) also present. Polycarbonate, however, can be safely recycled as a carbon source in the steel-making industry. Phenol derivatives are environmental pollutants, classified as volatile organic compounds (VOC). Studies show they are likely to facilitate ground level ozone formation and increase photo-chemical smog. In aquatic bodies, they can potentially accumulate in organisms. They are persistent in landfills, do not readily evaporate and would remain in the atmosphere.

## Effect of fungi

In 2001 a species of fungus in Belize, ''Geotrichum candidum'', was found to consume the polycarbonate found in compact discs (CD). This has prospects for bioremediation.