Terpolymerization studies. I. Terpolymerization of acrylonitrile, styrene, and esters of α-cyanocinnamic acid
✍ Scribed by Samuel H. Ronel; David H. Kohn
- Publisher
- John Wiley and Sons
- Year
- 1975
- Tongue
- English
- Weight
- 735 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0021-8995
No coin nor oath required. For personal study only.
✦ Synopsis
The terpolymerizations of acrylonitrile, styrene, and seven esters of a-cyanocinnamic acid were investigated up to low conversions. Polymerizations, carried out in bulk at 7OoC, were initiated by free radicals. The relationships between monomer feed and terpolymer composition were determined on a triangular coordinate graph as proposed by Slocombe. In all cases, there exists an azeotropic line, connecting the binary azeotrope of the pair acrylonitrile-styrene and that of the various pairs of styrene with the esters of a-cyanocinnamic acid, yet no real ternary azeotrope was found.
📜 SIMILAR VOLUMES
Free-radical solution terpolymerization of acrylamide, acrylic acid, and acrylonitrile was carried out in a mixture of dimethylformamide and water (60 : 40, v/v) at 85ЊC using benzoyl peroxide as the initiator. The polymers were characterized by elemental analysis, IR, 1 H-NMR, TGA, and viscosity me