Poly(methyl methacrylate)

Poly(methyl methacrylate)
Identifiers
CAS number 9011-14-7 YesY
Properties
Molecular formula (C5O2H8)n
Molar mass varies
Density 1.18 g/cm3[1]
Melting point

160 °C (320 °F)[2]

Boiling point

200.0 °C (392.0 °F)

Refractive index (nD) 1.4914 at 587.6 nm.[3]
 YesY (what is this?)  (verify)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Poly(methyl methacrylate) (PMMA) is a transparent thermoplastic, often used as a light or shatter-resistant alternative to glass. Chemically, it is the synthetic polymer of methyl methacrylate. The material was developed in 1928 in various laboratories, and was first brought to market in 1933 by Rohm and Haas Company, under the trademark Plexiglas[4]. It has since been sold under many different names.

PMMA is an economical alternative to polycarbonate (PC) when extreme strength is not necessary. Additionally, PMMA does not contain the potentially harmful bisphenol-A subunits found in polycarbonate. It is often preferred because of its moderate properties, easy handling and processing, and low cost, but behaves in a brittle manner when loaded, especially under an impact force, and is more prone to scratching compared to glass.

Contents

History

The first acrylic acid was created in 1843. Methacrylic acid, derived from acrylic acid, was formulated in 1865. The reaction between methacrylic acid and methanol results in the ester methyl methacrylate. The German chemists Fittig and Paul discovered in 1877 the polymerization process that turns methyl methacrylate into polymethyl methacrylate. In 1933 the German chemist Otto Röhm patented and registered the brand name PLEXIGLAS. In 1936 the first commercially viable production of acrylic safety glass began. During World War II acrylic glass was used for submarine periscopes, and windshields, canopies, and gun turrets for airplanes.[5]

Names

PMMA has been sold under a variety of brand names and generic names. It is often generically called acrylic glass[6], although it is chemically unrelated to glass. It is sometimes called simply acrylic[7], although acrylic can also refer to other polymers or copolymers containing polyacrylonitrile. Other notable trade names include:

Synthesis

PMMA is routinely produced by emulsion polymerization, solution polymerization and bulk polymerization. Generally radical initiation is used (including living polymerization methods), but anionic polymerization of PMMA can also be performed. To produce 1 kg (2.2 lb) of PMMA, about 2 kg (4.4 lb) of petroleum is needed.

Processing

The glass transition temperature of PMMA ranges from 85 to 165 °C (185 to 329 °F); the range is so wide because of the vast number of commercial compositions. The forming temperature starts at the glass transition temperature and goes up from there.[13] All common molding processes may be used, including injection molding, compression molding and extrusion. The highest quality PMMA sheets are produced by cell casting, but in this case, the polymerization and molding steps occur concurrently. The strength of the material is higher than molding grades owing to its extremely high molecular mass. Rubber toughening has been used to increase the strength of PMMA owing to its brittle behavior in response to applied loads.

Handling, cutting, and joining

PMMA can be joined using cyanoacrylate cement, more commonly known as superglue, with heat (melting), or by using solvents such as di- or trichloromethane to dissolve the plastic at the joint which then fuses and sets, forming an almost invisible weld. Scratches may easily be removed by polishing or by heating the surface of the material.

Laser cutting may be used to form intricate designs from PMMA sheets. PMMA vaporizes to gaseous compounds (including its monomers) upon laser cutting, so a very clean cut is made, and cutting is performed very easily. In this respect PMMA has an advantage over competing polymers such as polystyrene and polycarbonate, which require higher laser powers and give more messy and charred laser cuts.

In the majority of applications, it will not shatter. Rather, it breaks into large dull pieces. Softer and more easily scratched than glass, scratch-resistant coatings are often added to PMMA sheets to protect it (as well as possible other functions).

Properties

Skeletal structure of methyl methacrylate, the monomer that makes up PMMA

PMMA a is strong and lightweight material. It has a density of 1.17–1.20 g/cm3,[1][14] which is less than half that of glass.[1] It also has good impact strength, higher than both glass and polystyrene; however, PMMA's impact strength is still significantly lower than polycarbonate and some engineered polymers. PMMA ignites at 460 °C (860 °F) and burns, forming carbon dioxide, water, carbon monoxide and low molecular weight compounds, including formaldehyde.[15]

PMMA transmits up to 92% of visible light (3 mm thickness), and gives a reflection of about 4% from each of its surfaces on account of its refractive index (1.4914 at 587.6 nm).[3] It filters ultraviolet (UV) light at wavelengths below about 300 nm (similar to ordinary window glass). Some manufacturers[16] add coatings or additives to PMMA to improve absorption in the 300–400 nm range. PMMA passes infrared light of up to 2800 nm and blocks IR of longer wavelengths up to 25  µm. Colored PMMA varieities allow specific IR wavelengths to pass while blocking visible light (for remote control or heat sensor applications, for example).

PMMA swells and dissolves in many organic solvents; it also has poor resistance to many other chemicals on account of its easily hydrolyzed ester groups. Nevertheless, its environmental stability is superior to most other plastics such as polystyrene and polyethylene, and PMMA is therefore often the material of choice for outdoor applications.[17]

PMMA as maximum water absorption ratio of 0.3–0.4% by weight.[14] Tensile strength decreases with increased water absorption[18]. Its coefficient of thermal expansion is relatively high as (5–10)×10−5 /K.[19]

Modification of properties

Pure poly(methyl methacrylate) homopolymer is rarely sold as an end product, since it is not optimized for most applications. Rather, modified formulations with varying amounts of other comonomers, additives, and fillers are created for uses where specific properties are required. For example,

Poly(methyl acrylate)

The polymer of methyl acrylate, PMA or poly(methyl acrylate), is similar to poly(methyl methacrylate), except for the lack of methyl groups on the backbone carbon chain.[20] PMA is a soft white rubbery material that is softer than PMMA because its long polymer chains are thinner and smoother and can more easily slide past each other.

Uses

PMMA is a versatile material and has been used in a wide range of fields and applications.

Transparent glass substitute

Daylight redirection

Medical technologies and implants

Artistic and aesthetic uses

Other uses

High heel shoes made of Lucite
An electric bass guitar with its body made out of perspex

See also

References

  1. 1.0 1.1 1.2 Compare Materials: Acrylic and Soda-Lime Glass
  2. Smith & Hashemi 2006, p. 509.
  3. 3.0 3.1 Refractive index and related constants - Poly(methyl methacrylate) (PMMA, Acrylic glass)
  4. Rohm and Haas Innovation - Plexiglas Triumphs. Rohmhaas.com. Retrieved on 2010-08-29.
  5. "Acrylic Plastic: How Products are Made". http://www.enotes.com/how-products-encyclopedia/acrylic-plastic.  080515 enotes.com
  6. PMMA (Altuglas International) and Methacrylics. Arkema.com (2010-05-20). Retrieved on 2010-08-29.
  7. Plaskolite, Inc. | Innovative acrylic solutions: Acrylic Basics - FAQs. Plaskolite.com. Retrieved on 2010-08-29.
  8. "Altuglas International home page". http://www.altuglas.com/. Retrieved 2010-07-14. "more than a quarter of the world's production of PMMA" 
  9. 9.0 9.1 Lucite, Encyclopedia Britannica on-line
  10. Lucite, Merriam Webster dictionary
  11. Perspex, Merriam Webster dictionary
  12. "Plaskolite, Inc. home page". http://www.plaskolite.com/. Retrieved 2010-07-14. ""world's largest manufacturer of acrylic sheet"" 
  13. Ashby 2005, p. 519.
  14. 14.0 14.1 DATA TABLE FOR: Polymers: Commodity Polymers: PMMA
  15. "Preliminary studies on burning behavior of polymethylmethacrylate (PMMA)". http://cat.inist.fr/?aModele=afficheN&cpsidt=14365060.  090521 CAT.INIST
  16. Altuglas International Plexiglas UF-3 UF-4 and UF-5 sheets
  17. Myer Ezrin Plastics failure guide: cause and prevention, Hanser Verlag, 1996 ISBN 1569901848, p. 168
  18. Effects of Humidity History on the Tensile Deformation Behaviour in Poly(methyl-methacrylate) (PMMA) Films
  19. "Tangram Technology Ltd. -Polymer Data File -PMMA". http://www.tangram.co.uk/TI-Polymer-PMMA.html. 
  20. Polymethyl acrylate and polyethyl acrylate, Encyclopædia Britannica
  21. Kutz, Myer (2002). Handbook of Materials Selection. John Wiley & Sons. p. 341. ISBN 0471359246. 
  22. Terry Pepper, Seeing the Light, Illumination.
  23. Ken Yeang:Light Pipes: An Innovative Design Device for Bringing Natural Daylight and Illumination into Buildings with Deep Floor Plan, Nomination for the Far East Economic Review Asian Innovation Awards 2003
  24. Lighting up your workplace — Queensland student pipes light to your office cubicle, May 9, 2005
  25. Kenneth Yeang, World Cities Summit 2008, June 23—25, 2008, Singapore
  26. Modeling Attenuation versus Length in Practical Light Guides. doi:10.1582.LEUKOS.01.04.003. http://www.physics.ubc.ca/ssp/papers/Publications/Modelling%20attenuation%20versus%20length%20in%20practical%20light%20guides.pdf. 
  27. How Serraglaze works
  28. Glaze of light, Building Design Online, June 8, 2007
  29. Kaufmann, TJ; Jensen, ME; Ford, G; Gill, LL; Marx, WF; Kallmes, DF (2002). "Cardiovascular Effects of Polymethylmethacrylate Use in Percutaneous Vertebroplasty". American Journal of Neuroradiology 23 (4): 601–604. PMID 11950651. 
  30. Miller (1996). Review of Orthopaedics (4 ed.). Philadelphia: W. B. Saunders. p. 129. ISBN 0721659012. 
  31. F. J. Duarte (Ed.), Tunable Laser Applications (CRC, New York, 2009) Chapters 3 and 4.
  32. JS2K-PLT

Bibliography

External links