Meaning
Microscopic surface cracks form within amorphous polymers under sustained mechanical stress when the material reaches its limit for localized plastic deformation. A crazing mechanism occurs when high tensile loads cause polymer chains to pull apart into fibrils that span the gap between crack walls. These fibrils maintain structural integrity despite the void formation that precedes actual component rupture.
This phenomenon happens below the macroscopic glass transition temperature and acts as the primary precursor to brittle failure in rigid plastic parts.
Stress Threshold
Tensile forces concentrated at defects or sharp corners initiate internal fibrillation within the molecular structure. Molecular chains orient themselves along the direction of the applied load while the surrounding material retains its original configuration. Energy dissipation through this localized stretching prevents catastrophic fracture at early load stages.
Repeated cycles of expansion and contraction gradually degrade the strength of these fibrils until the cracks coalesce into a single failure plane.
Processing Variable
Injection pressure and cooling rates dictate the internal residual stress levels that govern the sensitivity of a molded piece to surface failure. Excessive packing pressure traps high levels of energy in the gate area which lowers the effective threshold for craze development. Rapid cooling cycles induce thermal gradients that lock molecular strain into the part geometry during solidification.
Adjusting nozzle temperatures or extending the hold phase reduces the density of these latent failure sites.
Material Specification
Resin suppliers define the environmental stress cracking resistance by exposing samples to chemical agents under constant strain. Datasheets categorize polymer grades by their inherent molecular weight and branching density which determine the capacity for fibril formation. Moulders use this information to select resins that withstand the anticipated service life of the finished assembly.
High molecular weight polymers offer superior resistance because the longer chains distribute stress across a larger volume of the material matrix.