Abstract
It is presented that cocrystallization leading to a solid solution occurs over a broad range of under-cooling in lamellae-forming blends of a nearly symmetric C-b-A with an asymmetric counterpart, while the corresponding homopolymer blends with similar molecular weight and composition exhibit phase-segregated crystallization. Cocrystallization in lamellae-forming blends are driven thermodynamically by the tendency of the short and long PB blocks to remain intimately mixed. The cocrystallization presents a scenario where a kinetics-dominated process found in homopolymer crystallization possibly turns into a thermodynamically favoured process in the C-b-A systems. Chain folding during crystallization in homopolymers is a kinetically driven phenomenon.
| Original language | English |
|---|---|
| Pages (from-to) | 8175-8179 |
| Number of pages | 5 |
| Journal | Macromolecules |
| Volume | 37 |
| Issue number | 22 |
| DOIs | |
| State | Published - 02 11 2004 |
| Externally published | Yes |
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