Terpolymerization of acrylamide, acrylic acid, and acrylonitrile: Synthesis and properties
β Scribed by Ismail Mathakiya; Veena Vangani; Animesh Kumar Rakshit
- Publisher
- John Wiley and Sons
- Year
- 1998
- Tongue
- English
- Weight
- 284 KB
- Volume
- 69
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
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 85ΠC using benzoyl peroxide as the initiator. The polymers were characterized by elemental analysis, IR, 1 H-NMR, TGA, and viscosity measurements. Elemental analysis data were used to evaluate the terpolymer composition. The reactivity ratios were determined by Fineman-Ross and Kelen-Tudos methods. The reactivity ratios (r) for the copolymerization of (1) acrylic acid / acrylonitrile with (2) acrylamide was found to be r 1 Γ 0.86 { 0.09 and r 2 Γ 1.93 { 0.03, respectively, by the Kelen-Tudos method. The Fineman-Ross method yielded a value of r 1 Γ 0.86 { 0.05 and r 2 Γ 1.94 { 0.09, respectively. The activation energy values for various stages of decomposition were calculated from TGA analysis. Voluminosity (V E ) and the shape factor (n) were also computed from the viscosity measurements in different ratios of the solvent mixture.
π SIMILAR VOLUMES
The radical copolymerization of acrylic acid with acrylamide was carried out at different monomer ratios in solution (DMF) at 60ΠC. The corresponding homopolymers were also synthesized to compare their metal ion binding abilities. All the copolymers were characterized by elemental analysis. The meta
Solution terpolymerization of styrene (Sty), acrylonitrile (AN) and copper acrylate (CuA) has been carried out in dimethylformamide at 90Β°C for 4 h using p-acetyl benzylidene triphenylarsonium ylide as radical initiator. 'H nuclear magnetic resonance (NMR), IR and elemental analysis have been used t