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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.
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.
Antimicrobial polymers containing quaternary ammonium as a side group are commonly synthesized from methacrylic monomers. [1] The benefit of these monomers is that the hydrophobicity, molecular weight, and surface charge can all be manipulated. [18] Hydrophobicity of the polymer has a strong effect on antimicrobial activity. [18]
The mass-average molecular mass, M w, is also related to the fractional monomer conversion, p, in step-growth polymerization (for the simplest case of linear polymers formed from two monomers in equimolar quantities) as per Carothers' equation: ¯ = + ¯ = (+), where M o is the molecular mass of the repeating unit.
The degree of polymerization, or DP, is the number of monomeric units in a macromolecule or polymer or oligomer molecule. [1] [2] [3]For a homopolymer, there is only one type of monomeric unit and the number-average degree of polymerization is given by ¯ ¯ = ¯, where ¯ is the number-average molecular weight and is the molecular weight of the monomer unit.
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It is applied to alkylated methacrylate monomers and the initiator is a silyl ketene acetal. New monomer adds to the initiator and to the active growing chain in a Michael reaction. With each addition of a monomer group the trimethylsilyl group is transferred to the end of the chain.
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