Prepolymer
In polymer chemistry, the term prepolymer or pre-polymer, refers to a monomer or system of monomers that have been reacted to an intermediate-molecular mass state. This material is capable of further polymerization by reactive groups to a fully cured, high-molecular-mass state. As such, mixtures of reactive polymers with un-reacted monomers may also be referred to as pre-polymers. The term "pre-polymer" and "polymer precursor" may be interchanged.[citation needed]
Polyurethane and polyurea prepolymers
[edit | edit source]In polyurethane chemistry, prepolymers and oligomers are frequently produced and then further formulated into CASE applications - Coatings, Adhesives, Sealants, and Elastomers. An isocyanate (usually a diisocyanate) is reacted with a polyol. All types of polyol may in theory be used to produce polyurethane prepolymers.[1][2][3][4][5] These then find use in CASE applications. When polyurethane dispersions are synthesized, a prepolymer is first produced usually modified with DMPA. In polyurea prepolymer production, instead of a polyol a polyamine is used.[6]
Lactic acid as a polymer precursor
[edit | edit source]Two molecules of lactic acid can be dehydrated to the cyclic molecule lactide, a lactone. A variety of catalysts can polymerise lactide to either heterotactic or syndiotactic polylactide, which as biodegradable polyesters with valuable (inter alia) medical properties are currently attracting much attention.[7]
Nowadays, lactic acid is used as a monomer for producing polylactic acid (PLA) which later has application as biodegradable plastic.[8] This kind of plastic is a good option for substituting conventional plastic produced from petrochemicals because of low emission of carbon dioxide. The commonly used process in producing lactic acid is via fermentation; to obtain the polylactic acid, the polymerization process follows.
See also
[edit | edit source]References
[edit | edit source]- ^ Howarth G.A "Synthesis of a legislation compliant corrosion protection coating system based on urethane, oxazolidine and waterborne epoxy technology" page 40 Master of Science Thesis April 1997 Imperial College London
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