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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.
Methylmalonic acid (MMA) is a chemical compound from the group of dicarboxylic acids. It consists of the basic structure of malonic acid and also carries a methyl group . The salts of methylmalonic acid are called methylmalonates .
Both the Mayo-Lewis equation and plot of the equation make evident that as monomer conversion increases, the copolymer composition will drift as the preferences for monomers change due to the interaction between reactivity ratios and the instantaneous concentration of each monomer. [2]
Monomer; Atom; Monomers are assigned short unique identifiers in internal HELM databases and can be represented by the identifier in strings. The approach is similar to that used in Simplified molecular-input line-entry system (SMILES). An exchangeable file format allows sharing of data between companies who have assigned different identifiers ...
An example of an ionomer, with carboxylate groups bound to a zinc cation. An ionomer (/ ˌ aɪ ˈ ɑː n ə m ər /) (iono-+ -mer) is a polymer composed of repeat units of both electrically neutral repeating units and ionized units covalently bonded to the polymer backbone as pendant group moieties.
The main application of size-exclusion chromatography is the fractionation of proteins and other water-soluble polymers, while gel permeation chromatography is used to analyze the molecular weight distribution of organic-soluble polymers.
Due to the larger size of macromonomers (as opposed to the size of regular monomers), synthetic challenges are brought about, giving reason for the analysis of polymerization mechanisms. Recent studies have shown that macromonomer polymerization kinetics and mechanisms can be significantly affected by the topological effect.