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Isocyanate is the functional group of atoms –N=C=O (1 nitrogen, 1 carbon, 1 oxygen), not to be confused with the cyanate functional group which is arranged as –O–C≡N. Any organic compound which contains an isocyanate group may also be referred to in brief as an isocyanate. An isocyanate may have more than one isocyanate group. An isocyanate that has two isocyanate groups is known as a diisocyanate. Diisocyanates are manufactured for reaction with polyols in the production of polyurethanes.
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Synthesis
The normal industrial route to the manufacture of diisocyanates, is to synthesize the desired molecular structure with amine functional groups at the positions to be occupied by the isocyanate groups. Reaction with phosgene replaces the amine groups with isocyanate groups.[1]
Common methods for the synthesis of isocyanates in the laboratory are the Curtius rearrangement of acyl azides and the Lossen rearrangement of hydroxamic acids.
Chemistry
The isocyanate group reacts with the hydroxyl functional group to form a urethane linkage. If a diisocyanate is reacted with a compound containing two or more hydroxyl groups (a polyol), long polymer chains are formed, known as polyurethanes.
The isocyanate group also reacts with the amine functional group. Reaction between a diisocyanate and a compound containing two or more amine groups, produces long polymer chains known as polyureas.
The isocyanate group can react with itself. Aliphatic diisocyanates can form trimers, known as biurets.
The isocyanate group reacts with water to form carbon dioxide (CO2). Carbon dioxide is used an an blowing agent (in situ) in order to produce polyurethane foams. (See Fundamentals to Polymer Science, An Introductory Text, p. 39, by Paul Painter and Michael Coleman, Second Edition, for more information).
Common compounds
Numbering of the ring atoms shown with blue numbers
A monofunctional isocyanate of industrial significance is methyl isocyanate (MIC), which is used in the manufacture of pesticides.
The global market for diisocyanates in the year 2000 was 4.4 million tonnes, of which 61.3% was methylene diphenyl diisocyanate (MDI), 34.1% was toluene diisocyanate (TDI), 3.4% was the total for hexamethylene diisocyanate (HDI) and isophorone diisocyanate (IPDI), and 1.2% was the total for various others.[1]
Hazards
The reactivity of isocyanates makes them harmful to living tissue. They are toxic and are known to cause asthma in humans, both through inhalation exposure and dermal contact. Exposure to isocyanates and their vapors should be avoided. For the safe handling of isocyanates,information is available from ISOPA[2], the European Diisocyanate and Polyol Producers Association.
See also
References
- ^ a b Randall, D (2002). The Polyurethanes Book. Wiley. ISBN 0-470-85041-8.
- ^ http://www.isopa.org ISOPA
External links
- NIOSH Safety and Health Topic: Isocyanates, from the website of the National Institute for Occupational Safety and Health (NIOSH)
- Health and Safety Executive, website of the UK Health and Safety Executive, useful search terms on this site - isocyanates, MVR, asthma
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Wikipedia content modification information:
- This page was last modified on 13 September 2008, at 14:54.
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