Abstract
The variation of glass transition temperature with molecular weight and chain-end composition for dendritic polyethers and polyesters was studied. A new and modified version of the chain-end free volume theory was derived to account for the large number of chain ends in these unusual structures. For both homopolymers and a variety of novel block copolymers, the experimental variation in Tg with molecular weight was found to correlate well with theoretical predictions, thus demonstrating the wide applicability of the chain-end free volume theory. The glass transition was found to be greatly affected by the nature of the chain ends and internal monomer units.
Original language | English (US) |
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Pages (from-to) | 1514-1519 |
Number of pages | 6 |
Journal | Macromolecules |
Volume | 26 |
Issue number | 7 |
DOIs | |
State | Published - 1993 |
Externally published | Yes |
ASJC Scopus subject areas
- Organic Chemistry
- Polymers and Plastics
- Inorganic Chemistry
- Materials Chemistry