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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.
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]
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.
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d is the average particle size, k includes parameters related to the reaction vessel design, D v is the reaction vessel diameter, D s is the diameter of the stirrer, R is the volume ratio of the monomer to the liquid matrix, N is the stirring speed, ν m and ν l are the viscosity of the monomer phase and liquid matrix respectively, ε is the ...
The monomer is a viscous liquid with a pungent odour. The first polymeric form of methacrylic acid was described in 1880 by Engelhorn and Fittig. The use of high purity monomers is required for proper polymerization conditions and therefore it is necessary to remove any inhibitors by extraction (phenolic inhibitors) or via distillation. [ 2 ]
Poly(ethyl methacrylate) (PEMA) is a hydrophobic synthetic acrylate polymer.It has properties similar to the more common PMMA, however it produces less heat during polymerization, has a lower modulus of elasticity and has an overall softer texture. [7]
10-Methacryloyloxydecyl dihydrogen phosphate (10-MDP, MDP Monomer) is a chemical compound used in dental adhesive materials. This organophosphate monomer was developed in 1981 by the Japanese company Kuraray for the preparation of dental adhesion polymers [ 1 ]