Synthesis and Characterisation of Poly(3-hydroxybutyrate-co-3-hydroxyvalerate)-b-poly(3-hydroxybutyrate-co-3-hydroxyvalerate) Multi-Block Copolymers Produced Using Diisocyanate Chemistry

被引:4
作者
Mai, Jingjing [1 ]
Pratt, Steven [1 ]
Laycock, Bronwyn [1 ]
Chan, Clement Matthew [1 ]
机构
[1] Univ Queensland, Sch Chem Engn, Brisbane, Qld 4072, Australia
基金
澳大利亚研究理事会;
关键词
polyhydroxyalkanoates; isocyanate chemistry; block copolymers; allophanates; cross-linking; POLY(ETHYLENE GLYCOL); MECHANICAL-PROPERTIES; PHYSICAL-PROPERTIES; GLASS-TRANSITION; MOLECULAR-WEIGHT; POLYHYDROXYALKANOATES; BIOSYNTHESIS; PHA; URETHANE)S;
D O I
10.3390/polym15153257
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Bacterially derived polyhydroxyalkanoates (PHAs) are attractive alternatives to commodity petroleum-derived plastics. The most common forms of the short chain length (scl-) PHAs, including poly(3-hydroxybutyrate) (P3HB) and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV), are currently limited in application because they are relatively stiff and brittle. The synthesis of PHA-b-PHA block copolymers could enhance the physical properties of PHAs. Therefore, this work explores the synthesis of PHBV-b-PHBV using relatively high molecular weight hydroxy-functionalised PHBV starting materials, coupled using facile diisocyanate chemistry, delivering industrially relevant high-molecular-weight block copolymeric products. A two-step synthesis approach was compared with a one-step approach, both of which resulted in successful block copolymer production. However, the two-step synthesis was shown to be less effective in building molecular weight. Both synthetic approaches were affected by additional isocyanate reactions resulting in the formation of by-products such as allophanate and likely biuret groups, which delivered partial cross-linking and higher molecular weights in the resulting multi-block products, identified for the first time as likely and significant by-products in such reactions, affecting the product performance.
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页数:15
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