Poly(methyl methacrylate)
Names | |
---|---|
IUPAC name
Poly(methyl 2-methylpropenoate) | |
Other names
Poly(methyl methacrylate) (PMMA) methyl methacrylate resin | |
Identifiers | |
9011-14-7 | |
3D model (Jmol) | Interactive image |
ECHA InfoCard | 100.112.313 |
KEGG | C19504 |
| |
Properties | |
(C5O2H8)n | |
Molar mass | varies |
Density | 1.18 g/cm3[1] |
Melting point | 160 °C (320 °F; 433 K)[2] |
Refractive index (nD) |
1.4905 at 589.3 nm[3] |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
verify (what is ?) | |
Infobox references | |
Poly(methyl methacrylate) (PMMA), also known as acrylic or acrylic glass as well as by the trade names Plexiglas, Acrylite, Lucite, and Perspex among several others (see below), is a transparent thermoplastic often used in sheet form as a lightweight or shatter-resistant alternative to glass. The same material can be utilised as a casting resin, in inks and coatings, and has many other uses.
Although not a type of familiar silica-based glass, the substance, like many thermoplastics, is often technically classified as a type of glass (in that it is a non-crystalline vitreous substance) hence its occasional historic designation as acrylic. Chemically, it is the synthetic polymer of methyl methacrylate. The material was developed in 1928 in several different laboratories by many chemists, such as William Chalmers, Otto Röhm and Walter Bauer, and was first brought to market in 1933 by the Rohm and Haas Company under the trademark Plexiglas.
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. Non-modified PMMA behaves in a brittle manner when under load, especially under an impact force, and is more prone to scratching than conventional inorganic glass, but modified PMMA is sometimes able to achieve high scratch and impact resistance.
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. In 1877 the German chemist Wilhelm Rudolph Fittig discovered the polymerization process that turns methyl methacrylate into polymethyl methacrylate. In 1933, the brand name "Plexiglas" was patented and registered by another German chemist, Otto Röhm. In 1936 Imperial Chemical Industries (now Lucite International) began the first commercially viable production of acrylic safety glass. During World War II both Allied and Axis forces used acrylic glass for submarine periscopes and aircraft windshields, canopies, and gun turrets. Airplane pilots whose eyes were damaged by flying shards of PMMA fared much better than those injured by standard glass, demonstrating the much-increased compatibility between human tissue and PMMA as compared to glass.[4]
Names
Common orthographic stylings include polymethyl methacrylate[5][6] and polymethylmethacrylate. The full chemical name is poly(methyl 2-methylpropenoate). (It is a common mistake to use "an" instead of "en".)
Although often called simply "acrylic", acrylic can also refer to other polymers or copolymers containing polyacrylonitrile. The other notable trade names include:
- Acrylite, a trademark of Evonik Cyro since 1976[7]
- Lucite (not leucite, although they sound alike), a trademark of DuPont, first registered in 1937[8]
- R-Cast, a trademark of Reynolds Polymer Technology. Founded in 1987 after spinning off from Reynolds & Taylor. They specialize in large scale and thick monolithic acrylic.[9]
- Plexiglas, a trademark of ELF Atochem, now a subsidiary of Arkema in the US,[10] a trademark of Evonik Röhm GmbH in other parts of the world.[11]
- Optix, a trademark of Plaskolite[10]
- Perspex, a trademark of Imperial Chemical Industries[10]
- Oroglas, a trademark of Rohm & Haas[12]
- Altuglas, also a trademark of Rohm & Haas[13]
- Cyrolite, a trademark of CYRO[10]
- Zylar, a trademark of Nova Chemicals[10]
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 (221 °F). 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.[14] 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 toughness of PMMA owing to its brittle behavior in response to applied loads.
Handling, cutting, and joining
PMMA can be joined using cyanoacrylate cement (commonly known as superglue), with heat (welding), or by using solvents such as di- or trichloromethane[15] 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 high internal stresses along the cut edge, which on exposure to solvents produce 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.[16] 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 3 mm thickness, two hours for up to 6 mm thickness, four hours for up to 12 mm thickness, and six hours for up to 20 mm 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 the 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][17] 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.[18]
PMMA transmits up to 92% of visible light (3 mm thickness), and gives a reflection of about 4% from each of its surfaces due to its refractive index (1.4905 at 589.3 nm).[3] It filters ultraviolet (UV) light at wavelengths below about 300 nm (similar to ordinary window glass). Some manufacturers[19] add coatings or additives to PMMA to improve absorption in the 300–400 nm range. PMMA passes infrared light of up to 2,800 nm and blocks IR of longer wavelengths up to 25,000 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 due to 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.[20]
PMMA has a maximum water absorption ratio of 0.3–0.4% by weight.[17] Tensile strength decreases with increased water absorption.[21] Its coefficient of thermal expansion is relatively high at (5–10)×10−5 K−1.[22]
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,
- A small amount of acrylate comonomers are routinely used in PMMA grades destined for heat processing, since this stabilizes the polymer to depolymerization ("unzipping") during processing.
- Comonomers such as butyl acrylate are often added to improve impact strength.
- Comonomers such as methacrylic acid can be added to increase the glass transition temperature of the polymer for higher temperature use such as in lighting applications.
- Plasticizers may be added to improve processing properties, lower the glass transition temperature, or improve impact properties.
- Dyes may be added to give color for decorative applications, or to protect against (or filter) UV light.
- Fillers may be added to improve cost-effectiveness.
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.[23] 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
Being transparent and durable, PMMA is a versatile material and has been used in a wide range of fields and applications such as: rear-lights and instrument clusters for vehicles, appliances and lenses for glasses. PMMA in the form of sheets affords shatter resistant panels for building windows, skylights, bullet proof security barriers, signs & displays, sanitary ware (bathtubs), LCD screens, furniture and many other applications. It is also used for coating polymers based on MMA provides outstanding stability against environmental conditions with reduced emission of VOC. Methacrylate polymers are used extensively in medical and dental applications where purity and stability are critical to performance.
Transparent glass substitute
- PMMA acrylic glass is commonly used for constructing residential and commercial aquariums. Designers started building big aquariums when poly(methyl methacrylate) could be used. It is less-used in other building types due to incidents such as the Summerland disaster.
- Acrylic is used for viewing ports and even complete pressure hulls of submersibles, such as the Alicia submarine's viewing sphere and the window of the bathyscaphe Trieste.
- PMMA is used in the lenses of exterior lights of automobiles.[24]
- The spectator protection in ice hockey rinks is made from PMMA.
- Historically, PMMA was an important improvement in the design of aircraft windows, making possible such iconic designs as the bombardier's transparent nose compartment in the Boeing B-17 Flying Fortress.
- Police vehicles for riot control often have the regular glass replaced with acrylic to protect the occupants from thrown objects.
- Acrylic is an important material in the making of certain lighthouse lenses.[25]
- PMMA was used for the roofing of the iconic compound in the Olympic Park for the 1972 Summer Olympics in Munich. It enabled a light and translucent construction underlining the democratic approach to the games.[26]
- PMMA (under the brand name "Lucite") was used for the ceiling of the Houston Astrodome.
Daylight redirection
- Laser cut acrylic panels have been used to redirect sunlight into a light pipe or tubular skylight and, from there, to spread it into a room.[27] Their developers Veronica Garcia Hansen, Ken Yeang, and Ian Edmonds were awarded the Far East Economic Review Innovation Award in bronze for this technology in 2003.[28][29]
- Attenuation being quite strong for distances over one meter (more than 90% intensity loss for a 3000 K source[30]), acrylic broadband light guides are then dedicated mostly to decorative uses.
- Pairs of acrylic sheets with a layer of microreplicated prisms between the sheets can have reflective and refractive properties that let them redirect part of incoming sunlight in dependence on its angle of incidence. Such panels act as miniature light shelves. Such panels have been commercialized for purposes of daylighting, to be used as a window or a canopy such that sunlight descending from the sky is directed to the ceiling or into the room rather than to the floor. This can lead to a higher illumination of the back part of a room, in particular when combined with a white ceiling, while having a slight impact on the view to the outside compared to normal glazing.[31][32]
Medical technologies and implants
- PMMA has a good degree of compatibility with human tissue, and it is used in the manufacture of rigid intraocular lenses which are implanted in the eye when the original lens has been removed in the treatment of cataracts. This compatibility was discovered by the English ophthalmologist Sir Harold Ridley in WWII RAF pilots, whose eyes had been riddled with PMMA splinters coming from the side windows of their Supermarine Spitfire fighters – the plastic scarcely caused any rejection, compared to glass splinters coming from aircraft such as the Hawker Hurricane.[33] Ridley had a lens manufactured by the Rayner company (Brighton & Hove, East Sussex) made from Perspex polymerised by ICI. On 29 November 1949 at St Thomas' Hospital, London, Ridley implanted the first intraocular lens at St Thomas's Hospital in London.[34]
In particular, acrylic-type contact lenses are useful for cataract surgery in patients that have recurrent ocular inflammation (uveitis), as acrylic material induce less inflammation.
- Eyeglass lenses are commonly made from PMMA.
- Historically, hard contact lenses were frequently made of this material. Soft contact lenses are often made of a related polymer, where acrylate monomers containing one or more hydroxyl groups make them hydrophilic.
- In orthopedic surgery, PMMA bone cement is used to affix implants and to remodel lost bone. It is supplied as a powder with liquid methyl methacrylate (MMA). Although PMMA is biologically compatible, MMA is considered to be an irritant and a possible carcinogen. PMMA has also been linked to cardiopulmonary events in the operating room due to hypotension.[35] Bone cement acts like a grout and not so much like a glue in arthroplasty. Although sticky, it does not bond to either the bone or the implant, it primarily fills the spaces between the prosthesis and the bone preventing motion. A disadvantage of this bone cement is that it heats up to 82.5 °C (180.5 °F) while setting that may cause thermal necrosis of neighboring tissue. A careful balance of initiators and monomers is needed to reduce the rate of polymerization, and thus the heat generated. A major consideration when using PMMA cement is the effect of stress shielding. Since PMMA has a Young's modulus between 1.8 and 3.1 GPa,[36] which is lower than that of natural bone (around 14 GPa for human cortical bone),[37] the stresses are loaded into the cement and so the bone no longer receives the mechanical signals to continue bone remodeling and so resorption will occur.[38]
- Dentures are often made of PMMA, and can be color-matched to the patient's teeth & gum tissue. PMMA is also used in the production of ocular prostheses, such as the osteo-odonto-keratoprosthesis.
- In cosmetic surgery, tiny PMMA microspheres suspended in some biological fluid are injected under the skin to reduce wrinkles or scars permanently.[39] PMMA is also used to create false "muscles" by body builders.
- Plombage is an outdated treatment of tuberculosis where the pleural space around an infected lung was filled with PMMA balls, in order to compress and collapse the affected lung.
- Emerging biotechnology and Biomedical research uses PMMA to create microfluidic lab-on-a-chip devices, which require 100 micrometre-wide geometries for routing liquids. These small geometries are amenable to using PMMA in a biochip fabrication process and offers moderate biocompatibility.
- Bioprocess chromatography columns use cast acrylic tubes as an alternative to glass and stainless steel. These are pressure rated and satisfy stringent requirements of materials for biocompatibility, toxicity and extractables.
Artistic and aesthetic uses
- Acrylic paint essentially consists of PMMA suspended in water; however since PMMA is hydrophobic, a substance with both hydrophobic and hydrophilic groups needs to be added to facilitate the suspension.
- Modern furniture makers, especially in the 1960s and 1970s, seeking to give their products a space age aesthetic, incorporated Lucite and other PMMA products into their designs, especially office chairs. Many other products (for example, guitars) are sometimes made with acrylic glass to make the commonly opaque objects translucent.
- Perspex has been used as a surface to paint on, for example by Salvador Dalí.
- Diasec is a process which uses acrylic glass as a substitute for normal glass in picture frames. This is done for its relatively low cost, light weight, shatter-resistance, aesthetics and because it can be ordered in larger sizes than standard picture framing glass.
- As early as 1939, Los Angeles-based Dutch sculptor Jan De Swart experimented with samples of Lucite sent to him by DuPont; De Swart created tools to work the Lucite for sculpture and mixed chemicals to bring about certain effects of color and refraction[40]
- From approximately the 1960s onward, sculptors and glass artists such as Jan Kubíček and Leroy Lamis began using acrylics, especially taking advantage of the material's flexibility, light weight, cost and its capacity to refract and filter light.
- In the 1950s and 1960s, Lucite was an extremely popular material for jewelry, with several companies specialized in creating high-quality pieces from this material. Lucite beads and ornaments are still sold by jewelry suppliers.
- Acrylic Sheets are produced in dozens of standard colors,[41] most commonly sold using color numbers developed by Rohm & Haas in the 1950s.
Other uses
- Acrylic is used in tanning beds as the transparent surface that separates the occupant from the tanning bulbs while tanning. The type of acrylic used in tanning beds is most often formulated from a special type of polymethyl methacrylate, a compound that allows the passage of ultraviolet rays
- Sheets of PMMA are commonly used in the sign industry to make flat cut out letters in thicknesses typically varying from 3 to 25 millimeters (0.1 to 1.0 in). These letters may be used alone to represent a company's name and/or logo, or they may be a component of illuminated channel letters. Acrylic is also used extensively throughout the sign industry as a component of wall signs where it may be a backplate, painted on the surface or the backside, a faceplate with additional raised lettering or even photographic images printed directly to it, or a spacer to separate sign components.
- PMMA was used in Laserdisc optical media. (CDs and DVDs use both acrylic and polycarbonate for impact resistance.)
- It is used as a light guide for the backlights in TFT-LCDs.
- Plastic optical fiber used for short distance communication is made from PMMA, and perfluorinated PMMA, clad with fluorinated PMMA, in situations where its flexibility and cheaper installation costs outweigh its poor heat tolerance and higher attenuation over glass fiber.
- PMMA, in a purified form, is used as the matrix in laser dye-doped organic solid-state gain media for tunable solid state dye lasers.[42]
- In semiconductor research and industry, PMMA aids as a resist in the electron beam lithography process. A solution consisting of the polymer in a solvent is used to spin coat silicon and other semiconducting and semi-insulating wafers with a thin film. Patterns on this can be made by an electron beam (using an electron microscope), deep UV light (shorter wavelength than the standard photolithography process), or X-rays. Exposure to these creates chain scission or (de-cross-linking) within the PMMA, allowing for the selective removal of exposed areas by a chemical developer, making it a positive photoresist. PMMA's advantage is that it allows for extremely high resolution patterns to be made. Smooth PMMA surface can be easily nanostructured by treatment in oxygen radio-frequency plasma[43] and nanostructured PMMA surface can be easily smoothed by vacuum ultraviolet (VUV) irradiation.[43]
- PMMA is used as a shield to stop beta radiation emitted from radioisotopes.
- Small strips of PMMA are used as dosimeter devices during the Gamma Irradiation process. The optical properties of PMMA change as the gamma dose increases, and can be measured with a spectrophotometer.
- A blacklight-reactive tattoo ink using PMMA microcapsules has been developed.[44]
- PMMA can be used as a dispersant for ceramic powders to stabilize colloidal suspensions in non-aqueous media. Due to its high viscosity upon dissolution, it can also be used as binder material for solution deposition processes, e.g. printing of solar cells.[45]
- PMMA has also been used extensively as a hybrid rocket fuel.
- In the 1960s, luthier Dan Armstrong developed a line of electric guitars and basses whose bodies were made completely of acrylic. These instruments were marketed under the Ampeg brand. Ibanez[46] and B.C. Rich have also made acrylic guitars.
- Ludwig-Musser makes a line of acrylic drums called Vistalites, well known as being used by Led Zeppelin drummer John Bonham.
- Artificial fingernails are sometimes made of acrylic.
- Some modern briar, and occasionally meerschaum, tobacco pipes sport stems made of Lucite.
- PMMA technology is utilized in roofing and waterproofing applications. By incorporating a polyester fleece sandwiched between two layers of catalyst-activated PMMA resin, a fully reinforced liquid membrane is created in situ.
- PMMA is a widely used material to create deal toys and financial tombstones.
-
High heel shoes made of Lucite
-
Picture of an electric bass guitar made from poly(methyl methacrylate)
Biodegradation
The Futuro house was made of fibreglass-reinforced polyester plastic, polyester-polyurethane, and poly(methylmethacrylate); one of them was found to be degrading by cyanobacteria and Archaea.[47][48]
See also
References
- 1 2 3 Polymethylmethacrylate (PMMA, Acrylic). Makeitfrom.com. Retrieved 2015-03-23.
- ↑ Smith, William F.; Hashemi, Javad (2006). Foundations of Materials Science and Engineering (4th ed.). McGraw-Hill. p. 509. ISBN 0-07-295358-6.
- 1 2 Refractive index and related constants – Poly(methyl methacrylate) (PMMA, Acrylic glass). Refractiveindex.info. Retrieved 2014-10-27.
- ↑ Schwarcz, Joe (6 November 2012), The Right Chemistry: 108 Enlightening, Nutritious, Health-Conscious and Occasionally Bizarre Inquiries into the Science of Daily Life, Doubleday Canada, p. 226, ISBN 978-0-385-67160-6
- ↑ Elsevier, Dorland's Illustrated Medical Dictionary, Elsevier
- ↑ Merriam-Webster, Merriam-Webster's Collegiate Dictionary, Merriam-Webster
- ↑ "The ACRYLITE® brand – ACRYLITE® – Colors, patterns and functions". Acrylite.net. Retrieved 2013-10-05.
- ↑ "Trademark Electronic Search System". TESS. US Patent and Trademark Office. p. Search for Registration Number 0350093. Retrieved 29 June 2014.
- ↑ "R-Cast® a Brief History". Reynoldspolymer.com.
- 1 2 3 4 5 Charles A. Harper; Edward M. Petrie (10 October 2003). Plastics Materials and Processes: A Concise Encyclopedia. John Wiley & Sons. p. 9. ISBN 978-0-471-45920-0.
- ↑ http://www.wipo.int/branddb/en/
- ↑ Reed Business Information (13 June 1974). "Misused materials stoked Sumerland fire". 62 (902). IPC Magazines: 684. ISSN 0262-4079.
- ↑ David K. Platt (1 January 2003). Engineering and High Performance Plastics Market Report: A Rapra Market Report. Smithers Rapra. p. 170. ISBN 978-1-85957-380-8.
- ↑ Ashby, Michael F. (2005). Materials Selection in Mechanical Design (3rd ed.). Elsevier. p. 519. ISBN 0-7506-6168-2.
- ↑ "Working with Plexiglas&®". science-projects.com.
- ↑ Andersen, Hans J. "Tensions in acrylics when laser cutting". Retrieved 23 December 2014.
- 1 2 DATA TABLE FOR: Polymers: Commodity Polymers: PMMA. Matbase.com. Retrieved 2012-05-09.
- ↑ Zeng, W. R.; Li, S. F.; Chow, W. K. (2002). "Preliminary Studies on Burning Behavior of Polymethylmethacrylate (PMMA)". Journal of Fire Sciences. 20 (4): 297–317. doi:10.1177/073490402762574749. INIST:14365060.
- ↑ Altuglas International Plexiglas UF-3 UF-4 and UF-5 sheets. Plexiglas.com. Retrieved 2012-05-09.
- ↑ Myer Ezrin Plastics Failure Guide: Cause and Prevention, Hanser Verlag, 1996 ISBN 1-56990-184-8, p. 168
- ↑ Ishiyama, Chiemi; Yamamoto, Yoshito; Higo, Yakichi (2005). Buchheit, T.; Minor, A.; Spolenak, R.; et al., eds. "Effects of Humidity History on the Tensile Deformation Behaviour of Poly(methyl –methacrylate) (PMMA) Films". MRS Proceedings. 875: O12.7. doi:10.1557/PROC-875-O12.7 (inactive 2015-01-09).
- ↑ "Tangram Technology Ltd. – Polymer Data File – PMMA".
- ↑ Polymethyl acrylate and polyethyl acrylate, Encyclopædia Britannica. Encyclopædia Britannica. Retrieved 2012-05-09.
- ↑ Kutz, Myer (2002). Handbook of Materials Selection. John Wiley & Sons. p. 341. ISBN 0-471-35924-6.
- ↑ Terry Pepper, Seeing the Light, Illumination. Terrypepper.com. Retrieved 2012-05-09.
- ↑ Deplazes, Andrea, ed. (2013). Constructing Architecture – Materials Processes Structures, A Handbook. Birkhäuser. ISBN 3038214523.
- ↑ Yeang, Ken. 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
- ↑ Lighting up your workplace – Queensland student pipes light to your office cubicle, May 9, 2005
- ↑ Kenneth Yeang, World Cities Summit 2008, June 23–25, 2008, Singapore
- ↑ Gerchikov, Victor; Mossman, Michele; Whitehead, Lorne (2005). "Modeling Attenuation versus Length in Practical Light Guides". LEUKOS. 1 (4): 47–59. doi:10.1582/LEUKOS.01.04.003 (inactive 2015-01-09).
- ↑ How Serraglaze works. Bendinglight.co.uk. Retrieved 2012-05-09.
- ↑ Glaze of light, Building Design Online, June 8, 2007
- ↑ Robert A. Meyers, "Molecular biology and biotechnology: a comprehensive desk reference", Wiley-VCH, 1995, p. 722 ISBN 1-56081-925-1
- ↑ Apple, David J (2006). Sir Harold Ridely and His Fight for Sight: He Changed the World So That We May Better See It. Thorofare NJ USA: Slack. ISBN 1-55642-786-7.
- ↑ Kaufmann, Timothy J.; Jensen, Mary E.; Ford, Gabriele; Gill, Lena L.; Marx, William F.; Kallmes, David F. (2002-04-01). "Cardiovascular Effects of Polymethylmethacrylate Use in Percutaneous Vertebroplasty". American Journal of Neuroradiology. 23 (4): 601–4. PMID 11950651.
- ↑ "MIT Material Property Database". Professors Carol Livermore and Joel Voldman. 20 February 2004. Retrieved 19 March 2013.
- ↑ Rho, Jae Young; Ashman, Richard B.; Turner, Charles H. (1993). "Young's modulus of trabecular and cortical bone material: Ultrasonic and microtensile measurements". Journal of Biomechanics. 26 (2): 111–9. doi:10.1016/0021-9290(93)90042-D. PMID 8429054.
- ↑ Miller (1996). Review of Orthopedics (4 ed.). Philadelphia: W. B. Saunders. p. 129. ISBN 0-7216-5901-2.
- ↑ "Filling in Wrinkles Safely". U.S. Food and Drug Administration. February 28, 2015. Retrieved 8 December 2015.
- ↑ de Swart, Ursula. My Life with Jan. Collection of Jock de Swart, Durango, CO
- ↑ Plexiglas ® Color Numbers. professionalplastics.com
- ↑ Duarte, F. J. (Ed.), Tunable Laser Applications (CRC, New York, 2009) Chapters 3 and 4.
- 1 2 Lapshin, R. V.; Alekhin, A. P.; Kirilenko, A. G.; Odintsov, S. L.; Krotkov, V. A. (2010). "Vacuum ultraviolet smoothing of nanometer-scale asperities of Poly(methyl methacrylate) surface". Journal of Surface Investigation. X-ray, Synchrotron and Neutron Techniques. 4 (1): 1–11. doi:10.1134/S1027451010010015.
- ↑ – Blacklight Tattoo Ink – Blacklight Tattoo Ink FAQ. Crazychameleonbodyartsupply.com. Retrieved 2012-05-09.
- ↑ Uhl, Alexander R.; Romanyuk, Yaroslav E.; Tiwari, Ayodhya N. (2011). "Thin film Cu(In,Ga)Se2 solar cells processed from solution pastes with polymethyl methacrylate binder". Thin Solid Films. 519 (21): 7259–63. Bibcode:2011TSF...519.7259U. doi:10.1016/j.tsf.2011.01.136.
- ↑ JS2K-PLT. Ibanezregister.com. Retrieved 2012-05-09.
- ↑ Cappitelli, Francesca; Principi, Pamela; Sorlini, Claudia (2006). "Biodeterioration of modern materials in contemporary collections: Can biotechnology help?". Trends in Biotechnology. 24 (8): 350–4. doi:10.1016/j.tibtech.2006.06.001. PMID 16782219.
- ↑ Rinaldi, Andrea (2006). "Saving a fragile legacy. Biotechnology and microbiology are increasingly used to preserve and restore the world's cultural heritage". EMBO Reports. 7 (11): 1075–9. doi:10.1038/sj.embor.7400844. PMC 1679785. PMID 17077862.
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