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Aspartic acid is prepared chemically or by the fermentation of carbohydrates. Currently, low molecular weight polyaspartic acids are prepared commercially by heating aspartic acid at high temperatures (>220°C) for several hours in the solid state. In an effort to develop a more rapid, continuous, melt polymerization scheme, aspartic acid was copolymerized with adipic, azelaic, sebacic, and dodecanedioic acids using a vented twin‐screw extruder. Copolymers having ratios of aspartic/diacid ≤16 andMwup to 9100 were prepared at temperatures of 240–260°C and residence times of only about 5 min.Mwgenerally increased with aspartic/diacid ratio but melt viscosities became very high and processing became difficult at ratios >16. Most of the copolymers exhibited inhibition of calcium carbonate precipitation at concentrations similar to that of pure polyaspartic acid and thus may find application as antiscalants.
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Shogren et al. (2008) studied this question.
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