1996•Journal of Applied Polymer ScienceRequires access

Solution polymerization of acrylonitrile with vinyl acids in dimethylformamide

P.N. Bajaj, Kushal Sen, Seyed Hajir Bahrami

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Abstract

Solution copolymerization of acrylonitrile (AN) with various vinyl acids, i.e., acrylic acid (AA), methacrylic acid (MAA), and itaconic acid (IA), was carried out in DMF at 70°C using α,α′-azobisisobutyronitrile (AIBN) as an initiator with an acidic monomer of 0.012–0.092 mol %. Copolymers were characterized by FTIR, CHN analysis, 1H-and 13C-NMR, and viscometry. The reactivity ratios were calculated using Fineman–Ross and Kelen–Tüdos methods. In all three systems, the value of r1 (AN) is much less than the value of r2. However, the r2 (MAA) is higher than r2 of (AA) and (IA). The reactivity ratios were calculated using Q and e schemes also. The results are in good agreement with experimentally calcualted data. The tacticity and sequence length distribution of these copolymers were calculated using 13C-NMR from CN and CH signals. It was observed that the isotacticity of acrylonitrile–itaconic acid copolymer P(AN–IA) with 8.2 mol % of a comonomer is lower than that of P(AN–MAA) with 10.3 mol % and P(AN–AA) with 7.61 mol %. © 1996 John Wiley & Sons, Inc.

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What this paper is about

Solution copolymerization of acrylonitrile (AN) with various vinyl acids, i.e., acrylic acid (AA), methacrylic acid (MAA), and itaconic acid (IA), was carried out in DMF at 70°C using α,α′-azobisisobutyronitrile (AIBN) as an initiator with an acidic monomer of 0.012–0.092 mol %. Copolymers were characterized by FTIR, CHN analysis, 1H-and 13C-NMR, and viscometry. The reactivity ratios were calculated using Fineman–Ross and Kelen–Tüdos methods. In all three systems, the value of r1 (AN) is much less than the value of r2. However, the r2 (MAA) is higher than r2 of (AA) and (IA). The reactivity ratios were calculated using Q and e schemes also. The results are in good agreement with experimentally calcualted data. The tacticity and sequence length distribution of these copolymers were calculated using 13C-NMR from CN and CH signals. It was observed that the isotacticity of acrylonitrile–itaconic acid copolymer P(AN–IA) with 8.2 mol % of a comonomer is lower than that of P(AN–MAA) with 10.3 mol % and P(AN–AA) with 7.61 mol %. © 1996 John Wiley & Sons, Inc.

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Available abstract

Solution copolymerization of acrylonitrile (AN) with various vinyl acids, i.e., acrylic acid (AA), methacrylic acid (MAA), and itaconic acid (IA), was carried out in DMF at 70°C using α,α′-azobisisobutyronitrile (AIBN) as an initiator with an acidic monomer of 0.012–0.092 mol %. Copolymers were characterized by FTIR, CHN analysis, 1H-and 13C-NMR, and viscometry. The reactivity ratios were calculated using Fineman–Ross and Kelen–Tüdos methods. In all three systems, the value of r1 (AN) is much less than the value of r2. However, the r2 (MAA) is higher than r2 of (AA) and (IA). The reactivity ratios were calculated using Q and e schemes also. The results are in good agreement with experimentally calcualted data. The tacticity and sequence length distribution of these copolymers were calculated using 13C-NMR from CN and CH signals. It was observed that the isotacticity of acrylonitrile–itaconic acid copolymer P(AN–IA) with 8.2 mol % of a comonomer is lower than that of P(AN–MAA) with 10.3 mol % and P(AN–AA) with 7.61 mol %. © 1996 John Wiley & Sons, Inc.

Key concepts: Acrylonitrile, Comonomer, Itaconic acid, Polymer chemistry, Copolymer, Methacrylic acid, Reactivity (psychology), Tacticity

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