Nucleation in polymer crystallization: A physical or a chemical mechanism?

✍ Scribed by J. P. Mercier

• Publisher: Society for Plastic Engineers
• Year: 1990
• Tongue: English
• Weight: 900 KB
• Volume: 30
• Category: Article
• ISSN: 0032-3888
• DOI: 10.1002/pen.760300504

✦ Synopsis

Abstract

Primary nucleation is in general heterogeneous in polymer crystallization. In unseeded polymers, the crystallization originates from a very small concentration (<0.1 percent) of unknown submicroscopic heterogeneous nuclei. Only in three cases have the nucleation mechanisms been identified with precision. The first example is self‐nucleation, which relates to the nucleation of a polymer melt by fragments of its own crystals previously present in the melt. Another example of heterogeneous nucleation is represented by epitaxial nucleation of polymers on inorganic and organic substrates recently established by Lotz and Wittmann. More recently, it was discovered that finely divided organic salts added to reactive polymers do not behave as inert heterogeneous substrates but rather dissolve and cut molten macromolecules producing ionic chain ends which precipitate into the melt and form organized aggregates which are the true nucleating species. It is clearly shown that mechanisms of physical and chemical origin are involved in heterogeneous primary nucleation of polymer crystallization.