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The modification of lactic acid based poly(ester-urethane) by copolymerization

✍ Scribed by Janne Kylmä; Mika Härkönen; Jukka V. Seppälä


Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
171 KB
Volume
63
Category
Article
ISSN
0021-8995

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✦ Synopsis


Copolymers of L-lactic acid (LLA) with DL-mandelic acid (DLMA), 4-hydroxybenzoic acid, 4-acetoxybenzoic acid, DL-malic acid, or anhydrous citric acid were synthesized via direct copolycondensation in the presence of 1,4-butanediol, using stannous octoate as catalyst. The effect of the comonomer and the comonomer ratio on polycondensation and the glass transition temperature were investigated. The glass transition temperature of amorphous poly(L-lactic acid-co-DL-mandelic acid) increased linearly from 33Њ to 56ЊC as the mandelic acid composition was increased from 0 to 45 mol %. For urethane synthesis, prepolymers of LLA and DLMA were condensation polymerized with compositions of 100/0, 90/10, and 80/20 (mol % in feed). The preparation of poly(ester-urethane) (PEU) was carried out in a stirred glass reactor, using 1,6-hexamethylene diisocyanate and isophorone diisocyanate in melt. The glass transition temperature of poly(L-lactic acid-co-DL-mandelic acid-urethanes) showed a marked increase with increased mandelic acid composition. The molecular weights of these urethanes were lower than for PEU based on poly(L-lactic acid). Such a depression in the degree of polymerization is attributed to the steric hindrance of the bulky phenyl group as a side chain of mandelic acid.


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