PLA–PHB–PLA Triblock Copolymers: Synthesis by Sequential Addition and Investigation of Mechanical and Rheological Properties

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Abstract

The dinuclear indium catalyst [(NNO)InCl]2(μ-OEt)(μ-Cl), previously reported to be highly active for the living ring-opening polymerization of cyclic esters lactide (LA) and β-butyrolactone (BBL), was used to generate a series of triblock copolymers of poly(lactic acid) (PLA) and poly(hydroxybutyrate) (PHB). Copolymers PLLA–PDLLA–PLLA and PLLA–PDLLA–PDLA, synthesized via sequential monomer addition, showed low molecular weight distributions and excellent correlation between the calculated and experiment molecular weights. Significantly, triblock copolymers of the type PLA–PHB–PLA were also synthesized for the first time through a sequential addition technique. Analysis of polymers after each addition of monomer showed that although only 85% conversion was achieved after addition of BBL, the remaining chain ends were active and addition of more lactide yielded a triblock. Rheological studies of PLLA–PHB–PDLA indicated solid like behavior even well above the temperature at which stereocomplex formation was observed. These elastomeric triblocks exhibited elongations at break 5–10 times greater than those of corresponding PLLA–PDLLA–PLDA triblocks.

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