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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

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✦ 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.


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Terpolymerization of acrylamide, acrylic
✍ Ismail Mathakiya; Veena Vangani; Animesh Kumar Rakshit 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 284 KB 👁 2 views

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