| Summary: | In the paper the results of synthesis of binary copolymers with different contents of monomer units by radical copolymerization of 1-chloro-3-piperidino-2-propylacrylate with acrylonitrile in organic solvent medium at 30-60°C in the presence of radical initiator using free-radical polymerization technique not up to high degrees of transformation by gravimetric method are given. Dinitrilazobisobisobutyric acid was used as the radical initiator. Water and dimethylformamide were used as solvent. Under these conditions in water the process proceeds heterogeneously, and in dimethylformamide homogeneously and with high speed. The synthesis rate of copolymers of 1-chloro-3-piperidino-2-propylacrylate with acrylonitrile in the studied solvents increases with increasing temperature. Experimental studies have shown that copolymerization does not proceed in the absence of the initiator and this indicates a radical nature of the reaction. The structure of synthesized compounds was confirmed by IR, NMR spectral analyses. The participation of multiple bonds of both monomers during copolymerization was determined. The composition of copolymers has been determined which indicates that the copolymer formed at early stages is enriched with 1-chloro-3-piperidino-2- propylacrylate units. The values of relative activities of monomers were calculated by Feinemann-Ross method. The found values of copolymerization constants 7:1=0.28, 7:2=0.62 and the value of product of copolymerization constants less than unity that both types of formed polymer radicals react much faster with foreign monomer than with their own.
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