Poly(3-hydroxybutyrate-co-3-hydroxyvalerate)/polycaprolactone (PHBV/PCL) polymer mixtures reinforced by cellulose nanocrystals (CNCs) have been obtained. To improve the CNC compatibility with the hydrophobic PHBV/PCL matrix, the CNC surface was modified by amphiphilic polymers, i.e., polyvinylpyrrolidone (PVP) and polyacrylamide (PAM). The polymer composites were characterized by FTIR, DSC, TG, XRD, microscopy, BET surface area, and tensile testing. The morphological, sorption, thermal, and mechanical properties of the obtained composites have been studied. It was found out that with an increase in the CNC content in the composites, the porosity of the films increased, which was reflected in an increase in their specific surface areas and water sorption. An analysis of the IR spectra confirms that hydrogen bonds can be formed between the CNC hydroxyl- and the -CO- groups of PCL and PHBV. The thermal decomposition of CNC in the PHBV/PCL/CNC composites starts at a much higher temperature than the decomposition of pure CNC. It was revealed that CNCs can either induce crystallization and the polymer crystallite growth or act as a compatibilizer of a mixture of the polymers causing their amorphization. The CNC addition significantly reduces the elongation and strength of the composites, but changes Young's modulus insignificantly, i.e., the mechanical properties of the composites are retained under conditions of small linear deformations. A molecular-dynamics simulation of several systems, starting from simplest binary (solvent-polymer) and finishing with multi-component (CNC-polymer mixture-solvent) systems, has been made. It is concluded that the surface modification of CNCs with amphiphilic polymers makes it possible to obtain the CNC composites with hydrophobic polymer matrices.
Keywords: cellulose nanocrystals; morphology; physicochemical properties; poly(3-hydroxybutyrate-co-3-hydroxyvalerate); polycaprolactone; polymer composites; structure–property relationship.