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MMA is a raw material for the manufacture of other methacrylates. These derivatives include ethyl methacrylate (EMA), butyl methacrylate (BMA) and 2-ethyl hexyl methacrylate (2-EHMA). Methacrylic acid (MAA) is used as a chemical intermediate as well as in the manufacture of coating polymers, construction chemicals and textile applications.
Radical polymerisation of unsaturated monomers is generally propagated by C-radicals. These can be effectively terminated by combining with other radicals to form neutral species and many true inhibitors operate through this mechanism. In the simplest example oxygen can be used as it exists naturally in its triplet state (i.e. it is a diradical).
The recovered monomers then are purified, but the costs and complexity have prevented this from becoming the norm. [30] Another approach binds monomers to the ends of long polymer chains. Those monomers detach when heated, triggering the chain to disassemble, with monomer yields of up to 90%, although the presence of dyes reduce this number.
Monomer to RAFT reagent: gives the expected degree of polymerization (that is, the number of monomer units in each polymer chain) and can be used to estimate the molecular weight of the polymer by Equation (1) (see below). [12] [14] RAFT reagent to initiator: determines the end groups on the polymer chains.
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Methacrylic acid, abbreviated MAA, is an organic compound with the formula CH 2 =C(CH 3)CO 2 H. This colorless, viscous liquid is a carboxylic acid with an acrid unpleasant odor.
It is a common monomer used in the production of epoxy resins. While typical home epoxies contain diglycidyl ether of bisphenol A (DGEBA), glycidyl methacrylate is instead used to provide epoxy functionalization to polyolefins and other acrylate resins. Glycidyl methacrylate is produced by several companies worldwide, including Dow Chemical. [2]
A colorless liquid, it is a common monomer for the preparation of acrylate polymers. [1] It is typically polymerized under free-radical conditions. [2] Ethyl methacrylate was first obtained by treating ethyl 2-hydroxyisobutyrate with phosphorus pentachloride in a dehydration reaction. [3]