ArticleMacromolecules2026
Decoupling the Roles of Chain Length, Entanglements, and Intermolecular Interactions on the Melt Memory of Semicrystalline Polar Homopolymers.
Article in Macromolecules, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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Abstract
In polymer crystals, chains are closely packed within unit cells. If they are heated above their melting point, they require a specific temperature and time to revert their ordered conformations to isotropic random coils in the melt. When the temperature is slightly above the melting point and all crystals have melted, the chains may retain a memory of the conformations they had in the crystals, i.e., they remember some of the extended or oriented conformations that they had in crystallographic registry. This causes enhanced recrystallization, a property denoted melt memory. Its exact nature remains a central question in polymer crystallization. Here, we combine small-angle X-ray scattering (SAXS) and differential scanning calorimetry (DSC) self-nucleation experiments to systematically investigate the molecular origin of melt memory in poly-(ε-caprolactone) (PCL) and poly-(ethylene oxide) (PEO) model samples, spanning a range of molecular weights from oligomers to highly entangled polymers. The entanglement molecular weights (
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