Crack propagation in amorphous polymers and their composites

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Abstract
The fracture energy of a polymer depends strongly on the viscoelastic responses of the material, and therefore is a function of temperature and crack velocity. The toughness of a composite is determined by the way in which the reinforcing filler modifies the energy dissipating mechanisms of the polymeric matrix. The fracture toughness of a variety of polymeric glasses and their composites with glass beads, glass fibers, and rubber particles was measured. The velocity of rapidly moving cracks and the crack propagation rates under controlled loading conditions were also measured. It was found that the crack propagation velocities in unfilled and glass bead filled materials were controlled by the longitudinal stress waves in the matrix and that the only effects of the glass beads were to blunt the crack tip and limit the viscous deformation. The effect on fracture toughness was relatively small and either positive or negative, depending on which of the above two factors dominated. The presence of rubber particles as a second phase lowered terminal crack propagation velocities and greatly increased the fracture toughness, indicating a crack retarding effect of the rubber particles. This is related to the induction of crazes in the matrix by the rubber phase. Glass fibers had a tendency to bridge the tip of a propagating crack, thereby greatly increasing the fracture toughness. In this case the work of fracture comes from a combination of the elastic strain energy stored in the fibers, the energy dissipated in debonding the fibers from the matrix, and the fracture energy of the matrix itself.