Abstract
Two oxetane-derived monomers 3-(2-cyanoethoxy)methyl- and 3-(methoxy(triethylenoxy)) methyl-3′-methyloxetane were prepared from the reaction of 3-methyl-3′-hydroxymethyloxetane with acrylonitrile and triethylene glycol monomethyl ether, respectively. Their homo- and copolyethers were synthesized with BF3 · Et2O/1,4-butanediol and trifluoromethane sulfonic acid as initiator through cationic ring-opening polymerization. The structure of the polymers was characterized by FTIR and1H NMR. The ratio of two repeating units incorporated into the copolymers is well consistent with the feed ratio. Regarding glass transition temperature (Tg), the DSC data imply that the resulting copolymers have a lower Tg than pure poly(ethylene oxide). Moreover, the TGA measurements reveal that they possess in general a high heat decomposition temperature. The ion conductivity of a sample (P-AN 20) is 1.07 × 10-5 S cm-1 at room temperature and 2.79 × 10-4 S cm-1 at 80°C, thus presenting the potential to meet the practical requirement of lithium ion batteries for polymer electrolytes.
Original language | English |
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Pages (from-to) | 1440-1448 |
Number of pages | 9 |
Journal | Polymer International |
Volume | 54 |
Issue number | 10 |
DOIs | |
Publication status | Published - Oct 2005 |
Keywords
- Cationic ring-opening polymerization
- Glass transition temperature
- Ion conductivity
- Oxetane-derived monomer
- Polymer electrolyte