Poly(methyl methacrylate)

Poly(methyl methacrylate)
Identifiers
CAS number 9011-14-7 Y
KEGG C19504 N
Jmol-3D images Image 1
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]
 N (verify) (what is: Y/N?)
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. It is sometimes called acrylic 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 including Lucite and Perspex.

The often-seen spelling poly(methyl 2-methylpropanoate) with -an- is an error for poly(methyl 2-methylpropenoate), based on propenoic acid.

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 conventional inorganic 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, 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, 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. PMMA produced by radical polymerization (all commercial PMMA) is atactic and completely amorphous.

Processing

The glass transition temperature (Tg) of atactic PMMA is 105 °C. The Tg values of commercial grades of PMMA range from 85 to 165 °C (185 to 329 °F); the range is so wide because of the vast number of commercial compositions which are copolymers with co-monomers other than methyl methacrylate. PMMA is thus an organic glass at room temperature — i.e., it is below its Tg. The forming temperature starts at the glass transition temperature and goes up from there.[12] 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 (welding), 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. However, the pulsed lasercutting introduces a high internal stresses along the cut edge, which when exposed to solvents produces undesirable "stress-crazing" at the cut edge and several millimetres deep. Even ammonium-based glass-cleaner and almost everything short of soap-and-water produces similar undesirable crazing, sometimes over the entire surface of the cut parts, at great distances from the stressed edge. Annealing the PMMA sheet/parts is therefore an obligatory post-processing step when intending to chemically bond lasercut parts together. This involves heating the parts in an air circulating oven from room temperature up to 90°C (at a rate of no more than 18 degrees per hour) down to room temperature (at a rate of no more than 12 degrees per hour). Temperature should be maintained as follows: one hour for 3mm thickness, two hours for up to 6mm thickness, four hours for up to 12mm thickness, and six hours for up to 20mm thickness. A rapid annealing cycle is reliable for thin sheets and involves placing them in a pre-heated oven to 80°C for one hour, then removing parts from oven and allowing to cool to room temperature. This added time component should be factored into the whole fabrication process, and the alternative Zero-rake sawcutting technique may provide better cost-effectiveness, unless complex non-straight line edges are required. 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. Since PMMA is 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).

Acrylate resin casting

Methyl methacrylate "synthetic resin" for casting (simply the bulk liquid chemical) may be used in conjunction with a polymerization catalyst such as MEKP, to produce hardened transparent PMMA in any shape, from a mold. Objects like insects or coins, or even dangerous chemicals in breakable quartz ampules, may be embedded in such "cast" blocks, for display and safe handling.

Properties

PMMA is a strong and lightweight material. It has a density of 1.17–1.20 g/cm3,[1][13] 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.[14]

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[15] 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 25000 nm. Colored PMMA varieties 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.[16]

PMMA has a maximum water absorption ratio of 0.3–0.4% by weight.[13] Tensile strength decreases with increased water absorption.[17] Its coefficient of thermal expansion is relatively high at (5–10)×10−5 /K.[18]

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.[19] 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

See also

References

  1. ^ a b c Compare Materials: Acrylic and Soda-Lime Glass
  2. ^ Smith & Hashemi 2006, p. 509.
  3. ^ a b 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. ^ Lucite, Merriam Webster dictionary
  8. ^ "Plexiglas". Altuglas International. http://www.plexiglas.com. 
  9. ^ "FAQ". Plaskolite. http://plaskolite.com/acrylic/faqs.cfm/Plaskolite. Retrieved 2011-01-23. "Manufacturer of Optix" 
  10. ^ Perspex, Merriam Webster dictionary
  11. ^ "Altuglas International". http://www.altuglas.com/. Retrieved 2010-07-14. "more than a quarter of the world's production of PMMA" 
  12. ^ Ashby 2005, p. 519.
  13. ^ a b DATA TABLE FOR: Polymers: Commodity Polymers: PMMA
  14. ^ "Preliminary studies on burning behavior of polymethylmethacrylate (PMMA)". http://cat.inist.fr/?aModele=afficheN&cpsidt=14365060.  090521 CAT.INIST
  15. ^ Altuglas International Plexiglas UF-3 UF-4 and UF-5 sheets
  16. ^ Myer Ezrin Plastics failure guide: cause and prevention, Hanser Verlag, 1996 ISBN 1569901848, p. 168
  17. ^ Effects of Humidity History on the Tensile Deformation Behaviour in Poly(methyl-methacrylate) (PMMA) Films
  18. ^ "Tangram Technology Ltd. -Polymer Data File -PMMA". http://www.tangram.co.uk/TI-Polymer-PMMA.html. 
  19. ^ Polymethyl acrylate and polyethyl acrylate, Encyclopædia Britannica
  20. ^ Kutz, Myer (2002). Handbook of Materials Selection. John Wiley & Sons. p. 341. ISBN 0471359246. 
  21. ^ Terry Pepper, Seeing the Light, Illumination.
  22. ^ 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
  23. ^ Lighting up your workplace — Queensland student pipes light to your office cubicle, May 9, 2005
  24. ^ Kenneth Yeang, World Cities Summit 2008, June 23—25, 2008, Singapore
  25. ^ 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. 
  26. ^ How Serraglaze works
  27. ^ Glaze of light, Building Design Online, June 8, 2007
  28. ^ Robert A. Meyers, "Molecular biology and biotechnology: a comprehensive desk reference", Wiley-VCH, 1995, p.722
  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 Orthopedics (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. ^ a b R. V. Lapshin, A. P. Alekhin, A. G. Kirilenko, S. L. Odintsov, V. A. Krotkov (2010). "Vacuum ultraviolet smoothing of nanometer-scale asperities of poly(methyl methacrylate) surface" (PDF). Journal of Surface Investigation. X-ray, Synchrotron and Neutron Techniques (Russia: Pleiades Publishing) 4 (1): 1–11. doi:10.1134/S1027451010010015. ISSN 1027-4510. http://www.nanoworld.org/homepages/lapshin/publications.htm#vacuum2010.  (Russian translation is available).
  33. ^ crazychameleonbodyartsupply.com - Blacklight Tattoo Ink - Blacklight Tattoo Ink FAQ
  34. ^ JS2K-PLT

Bibliography

External links