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Alternating Copolymerization of Propylene Oxide and Cyclohexene Oxide with Tricyclic Anhydrides: Access to Partially Renewable Aliphatic Polyesters with High Glass Transition Temperatures

机译:环氧丙烷和环己烯氧化物与三环酸酐的交替共聚:获得具有高玻璃化转变温度的部分可再生的脂肪族聚酯

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摘要

Renewable, biodegradable polymers, such as aliphatic polyesters, based on sustainable sources have attracted considerable interest as alternatives to petroleum-based polymers. One limiting factor in the development of aliphatic polyesters as replacements for these materials has been their relatively low glass transition temperatures (T-g). For example, commercially available poly(lactic add) has a T-g of approximately 60 degrees C. Epoxide/anhydride copolymerizations offer an alternative to the ring opening polymerization of lactones for the synthesis of aliphatic polyesters and allow for tuning of polymer properties through two distinct monomer sets. We synthesized six partially or fully renewable tricyclic anhydrides and copolymerized them with propylene oxide (PO) and cyclohexene oxide (CHO). By varying both the epoxide and the anhydride, we were able to tune the T-g of the resulting polymers over a nearly 120 degrees C range from 66 degrees C to an exceptionally high 184 degrees C. Polymers produced with PO had a lower range of T-g values (66-108 degrees C) and higher molecular weights up to 32.2 kDa, while those produced with CHO had higher T-g values (124-184 degrees C) and lower molecular weights, showing the profound influence of both monomer sets. To the best of our knowledge, these are the highest T-g values reported for entirely aliphatic polyesters.
机译:作为基于石油的聚合物的替代品,基于可持续资源的可再生,可生物降解的聚合物(例如脂族聚酯)引起了极大的兴趣。在脂肪族聚酯作为这些材料的替代品发展中的一个限制因素是它们相对较低的玻璃化转变温度(T-g)。例如,市售的聚(乳酸添加物)的Tg为约60℃。环氧/酸酐共聚为内酯的开环聚合提供了一种替代方案,用于合成脂族聚酯,并允许通过两种不同的单体调节聚合物的性质。套。我们合成了六种部分或完全可再生的三环酸酐,并将它们与环氧丙烷(PO)和环己烯氧化物(CHO)共聚。通过改变环氧化物和酸酐,我们能够在接近120摄氏度的范围内(从66摄氏度到184摄氏度)调节所得聚合物的Tg。用PO生产的聚合物的Tg值范围较小(66-108摄氏度)和更高的分子量,最高可达32.2 kDa,而用CHO生产的那些具有更高的Tg值(124-184摄氏度)和更低的分子量,显示了这两种单体的深刻影响。据我们所知,这些是报道的全脂族聚酯的最高T-g值。

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