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- W2333799118 abstract "Using racemic starting materials rather than single-isomer ones and employing a racemic catalyst, chemists at Michigan State University, East Lansing, have polymerized cyclic dimers of lactic acid to stereoregular polymer chains [ J. Am. Chem. Soc. , 122 , 1552 (2000)]. Their achievement produces a crystalline polylactic acid resin with physical properties that are superior to those of polymers with unordered configurations. The result is one more step forward in efforts to develop green biodegradable plastics from renewable resources as alternatives to polymers derived from petrochemicals. Potential uses for polylactic acid include cast, oriented, and blown films; fibers and nonwoven fabrics; coatings for paper and cardboard; and thermoformed, injection-molded, or blow-molded containers. The MSU publication comes hot on the heels of the introduction of commercial polylactic acid resin by Cargill Dow Polymers, Minnetonka, Minn. (C&EN, Jan. 17, page 13). Cargill Dow is a joint venture of Dow Chemical and..." @default.
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- W2333799118 date "2000-02-28" @default.
- W2333799118 modified "2023-09-27" @default.
- W2333799118 title "Racemic tack yields stereoregular polylactic acid" @default.
- W2333799118 doi "https://doi.org/10.1021/cen-v078n009.p014" @default.
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