## Abstract The reaction of rigid poly(vinyl chloride) (PVC) with iodide, hydroxide, azide, and thiocyanate as nucleophiles (Nu) in ethylene glycol (EG) resulted in the substitution of Cl by Nu additional to the elimination of HCl, leading to the dehydrochlorination of the rigid PVC. High substitut
Thermosets obtained by chemical modification of poly(epichlorohydrin) with vinyl-terminated aromatic carboxylates
✍ Scribed by Jose Antonio Reina; Angels Serra; Virginia Cádiz
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 660 KB
- Volume
- 197
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
Poly(epichlorohydrin) was modified in a high extent with several vinyl‐terminated aromatic potassium carboxylates (4‐(2‐propenyloxy)benzoate, 4‐(5‐hexenyloxy)benzoate, 3‐(2‐propenyloxy)‐2‐naphthoate, 3‐(5‐hexenyloxy)‐2‐naphthoate and 2‐(thioallyl)nicotinate) under solid‐liquid phase‐transfer conditions. Simultaneously with this substitution reaction, cleavage and crosslinking side reactions occurred. The polymers obtained were characterized by NMR, IR, elemental analysis, viscosimetry, size exclusion chromatography (SEC), differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA). Then, crosslinked materials were obtained by curing mixtures of these linear polymers with 10% w/w of a radical initiator (dicumyl peroxide or 2,2′‐azoisobutyronitrile) on a DSC device. Finally, the thermal stability of the thermosetting materials was tested by TGA, and the Arrhenius kinetic parameters were determined for dicumyl peroxide initiated crosslinking processes by calorimetric measurements.
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