Polymer International · 2010 · 39 citations · 27 references
Natural SciencesChemical EngineeringMaterials SciencePolymer ChemistryPolymer EngineeringPolymer MaterialsBiodegradable PolymersPolymer CharacterizationPolymer FunctionalizationPolymer StructurePolymerization ChemistryThermoplastic PolymersBiodegradable MaterialsEnzymatic DegradationFlexural StrengthPolymer BiodegradationTensile StrengthThermal PropertiesThermal StabilityThermogravimetric Data Analysis
Abstract In this exploration of novel biodegradable polyesters, multiblock copolymers based on poly(butylene succinate) (PBS) and poly(1,2‐propylene terephthalate) (PPT) were successfully synthesized with hexamethylene diisocyanate as a chain extender. The amorphous and rigid PPT segment was chosen to modify PBS. The structures of the polymers were characterized using 1 H NMR and 13 C NMR spectroscopy, gel permeation chromatography and wide‐angle X‐ray diffraction; the physical properties were investigated using thermogravimetric analysis, differential scanning calorimetry, mechanical testing and enzymatic degradation. The results indicate that the copolymers possess satisfactory mechanical and thermal properties, with impact strength 186% higher than that of PBS homopolymer, while tensile strength, flexural strength, thermal stability and melting point ( T m ) are slightly decreased. Crystallization and biodegradation rates are still acceptable at 5 wt% PPT, although they are decreased by the introduction of PPT. The addition of appropriate amounts of PPT can improve the impact strength effectively without an obviously deleterious effect on tensile strength, flexural strength, thermal stability, T m , crystallization rate and biodegradability. This study describes a convenient route to novel multiblock copolymers comprising crystallizable aliphatic and amorphous aromatic polyesters, which are promising for commercialization as biodegradable materials. Copyright © 2011 Society of Chemical Industry
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Polymer synthesis by microorganisms: technology and economics
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