Nov. 27, 2024
acrylic, any of a broad array of synthetic resins and fibres that are based on derivatives of acrylic and methacrylic acid. Both acrylic acid (CH2=CHCO2H) and methacrylic acid (CH2=C[CH3]CO2H) have been synthesized since the mid-19th century, but the practical potential of materials related to these compounds became apparent only about , when German chemist Otto Röhm published doctoral research on polymers of acrylic esters. Beginning on a commercial basis in the s, esters of acrylic acid were polymerized to form the polyacrylate resins, which are now important constituents of acrylic paints, and methacrylic acid esters were polymerized to polymethyl methacrylate, a clear plastic sold under trademarks such as Plexiglas and Perspex. In Orlon, the first commercially successful acrylic fibre, was introduced by E.I. du Pont de Nemours & Company (now DuPont Company). Acrylic and modacrylic fibres are based on polyacrylonitrile.
Other acrylics include cyanoacrylate resins, made into fast-acting adhesives; poly-2-hydroxyethyl methacrylate, abbreviated polyHEMA, made into soft contact lenses; polyacrylamide resins, used as flocculents in water clarification; and rubber products made of polyacrylate elastomer.
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Description
Acrylic BraceletMFA# .112
An umbrella term used to describe a family of thermoplastic materials that are the result of polymerizing or co-polymerizing vinyl monomers with a carbonyl or nitrile group attached, including but not limited to Acrylic acid, Methacrylic acid, or Acrylonitrile. The generic description of these materials is represented as: (CH2=CHCO2R), with R representing the organic group[1]. Acrylic polymers were first prepared in by the Swiss chemist Georg W.A. Kahlbaum. In , in Germany, Otto Röhm described his acrylate synthesis work in Polymerization products of acrylic acid, his doctoral thesis then later patented the process in [2]. Polymethyl methacrylate was first marketed by Rohm and Haas in Germany in . Acrylics have been sold by Rohm & Haas, ICI in England and DuPont in the U.S. since as glass substitutes (Plexigum®, Plexiglas®, Perspex® and Lucite® ) and as adhesives, varnishes, and paint media (Acryloid® F-10, Lucite® 44, Acryloid® B-72). Magna solvent-soluble acrylic artist paints were first sold in by Bocour, while Liquitex, an acrylic emulsion paint, was first marketed in . The first Acrylic fiber, Orlon®, was introduced in .
Synonyms and Related Terms
acrylics; acrylate; methacrylate; résine acrylique (Fr.); resina acrilica (It.); polímero acrílico (Esp.); resina acrílica (Esp.); acrílico (Esp.); resina acrílica (Port.)
Examples: Acryloid® [Rohm & Haas];Plexigum® [Rohm & Haas]; Lucite® [DuPont]; Paraloid® [Rohm & Haas]; Elvacite® [DuPont]; Plexiglas® [Rohm & Haas]; Perspex®; Magna [Bocour]; Liquitex [Permanent Pigments]; Shiva [Shiva]; Hyplar Acrylic Colors[Grumbacher]; Aqua-tec [Bocour]
Applications
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Personal Risks
Collection Risks
Some acrylic pressure sensitive adhesives that are designed NOT to dry, may give off acetic acid and acrylic acid; both are corrosive.
Environmental Risks
Physical and Chemical Properties
Acrylic resins range from soft, tacky materials to hard solids that are glossy, optically clear and have good shock and water resistance. Acrylics tend to be stable to outdoor weathering and resistant to some chemicals including mild acids and bases.
Soluble in mineral spirits, turpentine, aromatic hydrocarbons, chlorinated hydrocarbons, esters, and ketones.
Insoluble in water, ethanol.
Softening points (Tg in C) are:
Refractive Index = 1.5
Comparisons
Physical Properties for Selected Thermoplastic Resins
General Characteristics of Polymers
Resources and Citations
Feller, R.L., N. Stolow, and E.H. Jones. . On picture varnishes and their solvents. Revised and enlarged ed. Washington, D.C.: National Gallery of Art.
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