AbstractThe chain entanglement states in high density, linear low density, and low density polyethylenes (HDPE, LLDPE, and LDPE) have been modified by recovering the polymers from solutions in trichlorobenzene (TCB) andp‐xylene. In the thermodynamically good solvent, TCB, the entanglement density is assumed to be sharply reduced, a condition which is carried over to the corresponding solids. These display transient, but large increments in tensile moduli, slight changes in stress at rupture, and decreases in dynamic mechanical parameters and in elongation at rupture. Scanning calorimetry also shows these solids to have reduced crystallinity. Much smaller property modifications are noted in corresponding samples recovered fromp‐xylene. This liquid is a poorer solvent, particularly for HDPE and LLDPE. The results indicate that property modifications due to deliberate changes in the entanglement states of the polymers are a general phenomenon in the polyethylenes, and the magnitude of property changes depends on parameters of the molecular weight distribution. Chain branching does not seem to be a leading factor in the sensitivity of properties to modifications in the entanglement states. The property modifications produced by the present solution treatments are viewed as guides to the magnitude and duration of shear refining effects to be expected in HDPE, LLDPE, and LDPE polym
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