Preparation and Properties of Thermally Stable Lignin-based Copolymer/PP Blends by Melt Process

Abstract

Lignin-based polycaprolactone (LigPCL) copolymer was synthesized by both the ring opening reaction of caprolactone with the hydroxyl groups in the lignin and the concomitant polymerization of s-caprolactone. FTIR spectra showed C=0 (1755 cm(-1)) and C-O (1202 cm(-1)) peaks confirming that the esterification reaction took place successfully between lignin and s-caprolactone. T-2, at which the weight loss of 2% occurs, of pristine lignin and LigPCL were measured as 63 and 211 degrees C, respectively, and so the synthesized LigPCL had superior thermal stability to the lignin PP/LigPCL blends were prepared at various contents of LigPCL up to 30 wt% by a melt extrusion process. In proportion to the content of the LigPCL, tensile strengths, flexural strengths, and tensile modulus of PP/LigPCL blends greatly decreased, but elongations at break of those greatly increased. To improve the compatibility between PP and LigPCL, maleic anhydride-grafted polypropylene (PP-g-MA) was added. SEM images for the fracture surfaces of the blends showed that the PP-g-MA was effective in reducing the domain size of dispersed phase. Thus, T2, tensile strength, tensile modulus, and elongation at break of a 70/30 blend of PP/LigPCL were enhanced by 6 degrees C, 17%, 31%, and 79%, respectively, by the addition of PP-g-MA. This work clearly demonstrates that thermoplastic LigPCL could be desirably synthesized and applied for value added and eco-friendly products through common melt processes used for polymer blend or composites manufacturing.