Dynamic bulk properties of urethane acrylate copolymer networks were tested by dynamic mechanical thermal analysis (DMTA) at I Hz. Three urethane acrylates of different chain length were copolymerized with methyl acrylate and two diacrylates and storage moduli and glass transition temperature measur
Dynamic-mechanical properties and cross-polarized, proton-enhanced, magic angle spinning 13C-NMR time constants of urethane acrylates—1. Homopolymer networks
✍ Scribed by A.B. Clayton; P.E.M. Allen; B.J. Keon; D.R.G. Williams
- Publisher
- Elsevier Science
- Year
- 1993
- Tongue
- English
- Weight
- 636 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0014-3057
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✦ Synopsis
Dynamic-mechanical properties have been measured for a series of urethane acrylates containing polyether and polyester soft segments. Polymer glass transition temperatures predicted from a crosslinking relation showed better agreement with experimental Tg values than those obtained from applying the Fox equation to hard and soft segments in the polymer. Proton-enhanced, magic angle spinning ~3C-NMR time constants were obtained for a polyether soft segment urethane acrylate series. Increasing soft segment molecular weight resulted in a release of both near static and high frequency (mid-kHz) components of motion in the soft segment.
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