Renewable Unsaturated Polyesters from Muconic Acid

粘酸 高分子化学 聚酯纤维 对苯二甲酸 二羧酸 聚丁二酸丁二醇酯 琥珀酸 材料科学 玻璃化转变 缩聚物 烯烃 聚合 有机化学 聚合物 己二酸 化学 催化作用
作者
Nicholas A. Rorrer,John R. Dorgan,Derek R. Vardon,Chelsea R. Martinez,Yuan Yang,Gregg T. Beckham
出处
期刊:ACS Sustainable Chemistry & Engineering [American Chemical Society]
卷期号:4 (12): 6867-6876 被引量:76
标识
DOI:10.1021/acssuschemeng.6b01820
摘要

cis,cis-Muconic acid is an unsaturated dicarboxylic acid that can be produced in high yields via biological conversion of sugars and lignin-derived aromatic compounds. Muconic acid is often targeted as an intermediate to direct replacement monomers such as adipic or terephthalic acid. However, the alkene groups in muconic acid provide incentive for its direct use in polymers, for example, in the synthesis of unsaturated polyester resins. Here, biologically derived muconic acid is incorporated into polyesters via condensation polymerization using the homologous series of poly(ethylene succinate), poly(propylene succinate), poly(butylene succinate), and poly(hexylene succinate). Additionally, dimethyl cis,cis-muconate is synthesized and subsequently incorporated into poly(butylene succinate). NMR measurements demonstrate that alkene bonds are present in the polymer backbones. In all cases, the glass transition temperatures are increased whereas the melting and degradation temperatures are decreased. In the case of poly(butylene succinate), utilization of neat muconic acid yields substoichiometric incorporation consistent with a tapered copolymer structure, whereas the muconate diester exhibits stoichiometric incorporation and a random copolymer structure based on thermal and mechanical properties. Prototypical fiberglass panels were produced by infusing a mixture of low molecular weight poly(butylene succinate-co-muconate) and styrene into a woven glass mat and thermally initiating polymerization resulting in thermoset composites with shear moduli in excess of 30 GPa, a value typical of commercial composites. The increased glass transition temperatures with increasing mucconic incorporation leads to improved composites properties. We find that the molecular tunability of poly(butylene succinate-co-muconate) as a tapered or random copolymer enables the tunability of composite properties. Overall, this study demonstrates the utility of muconic acid as a monomer suitable for direct use in commercial composites.
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