A comparison is made of the chain conformational distribution of hydroxyterminated poly(propylene glycol) (PPG) and poly(ethylene glycol) (PEG) with their methoxy-terminated derivatives. The significant end-group dependence on the glass transition temperature in PPG was observed by differential scan
Modification of unsaturated polyesters by poly(ethylene glycol) end groups
β Scribed by Uwe Schulze; Mikael Skrifvars; Norbert Reichelt; Hans-Werner Schmidt
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 229 KB
- Volume
- 64
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
This article reports on the modification of unsaturated polyesters by poly (ethylene glycol) end groups in order to influence the solution behavior in styrene and to modify mechanical properties of the cured resin. The synthesis was done by the reaction of a carboxyl-terminated unsaturated polyester with various poly(ethylene glycol) mono-methyl ethers of molecular weights from 350 to 2000 g/mol. The characterization and curing properties of the synthesized block copolymers are presented. The glass transition temperatures decrease with increasing length of the poly(ethylene glycol) end groups. The introduction of long poly(ethylene glycol) end groups (2000 g/ mol) leads to a phase separated and partly crystalline block copolymer with a melting point of 48ΠC. The block copolymers can be easily diluted in styrene to create the curable resins. The mixtures containing the block copolymers with the short poly(ethylene glycol) end groups (350 and 550 g/mol) could be cured in a reasonably short time. Compared to commercial unsaturated polyesters the mechanical testing revealed that the tensile strength is decreasing while the elongation is increasing.
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