Transforming Polylactide into Value-Added Materials

被引:92
|
作者
Leibfarth, Frank A. [1 ]
Moreno, Nicholas [1 ]
Hawker, Alex P. [2 ]
Shand, Justin D. [2 ]
机构
[1] Univ Calif Santa Barbara, Dept Chem & Biochem, Mat Res Lab, Santa Barbara, CA 93101 USA
[2] Laguna Blanca High Sch, Santa Barbara, CA 93110 USA
基金
美国国家科学基金会;
关键词
biodegradable; depolymerization; glycolate ester; lactate ester; organic catalysis; polyesters; polyglycolide; polylactide; recycling; transesterification; RING-OPENING POLYMERIZATION; LACTIC-ACID; RENEWABLE RESOURCES; ETHYL LACTATE; POLYMERS; DEGRADATION; ESTERIFICATION; POLYCARBONATES; COMPOSITES; HYDROLYSIS;
D O I
10.1002/pola.26303
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The production of chemical building blocks and polymer precursors from biorenewable and sustainable resources is an attractive method to bypass traditional fossil fuel derived materials. Accordingly, we report the organocatalytic recycling of postconsumer polylactide (PLA) into value-added small molecules. This strategy, using the highly active transesterification catalyst triazabicyclodecene, is shown to completely depolymerize PLA in the presence of various alcohols into valuable lactate esters. Using previously used PLA packaging material, the depolymerization is complete in minutes at room temperature and fully retains the stereochemistry of the lactate species. Further, the modularity and utility of this methodology with respect to polyester substrate is detailed by using a variety of functional alcohols to depolymerize both PLA and polyglycolide, with the corresponding ester small-molecules being used to make new polymeric materials. The opportunities to transform waste streams into value-added chemicals and new materials through simple and versatile chemistry hold significant potential to extend the lifecycle of renewable chemical feedstocks. (C) 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 50: 4814-4822, 2012
引用
收藏
页码:4814 / 4822
页数:9
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