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Copolymerization of dienic hydrocarbons with vinyl ethers

Communication 1. peculiar features of the copolymerization of chloroprene with vinyl ethers

  • Organic and Biological Chemistry
  • Published:
Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Summary

  1. 1.

    n investigation was made of the emulsion and mass copolymerization of chloroprene with isopropyl vinyl ether at various temperatures.

  2. 2.

    n presence of initiators for radical copolymerization, two mechanisms operate simultaneously; a) copolymerization by the radical mechanism, and b) copolymerization by the cationic mechanism.

  3. 3.

    he relative amounts of copolymers of the radical and cationic types are considerably dependent on the polymerization conditions. Under all conditions the copolymer of the cationic type predominates.

  4. 4.

    Conditions were found which make it possible for the process to be directed in a single direction with formation of copolymers containing tip to 95–98% of the vinyl ether (molecular weight 60,000–90,000) or 80–90% of chloroprene (molecular weight 60,000).

  5. 5.

    The radical-copolymerization constants of the system were determined; r1 = 0.164± 0.043; r2 = 11.45 ± 0.54. The existence of two constants is explained as the result of the effect of the penultimate monomer unit (M2).

  6. 6.

    The emulsion copolymers corresponded in composition to a mechanism of radical copolymerization.

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Literature cited

  1. F. R. Mayo and F. M. Lewis, J. Am. Chem. Soc. 66, 9, 1594 (1944).

    Google Scholar 

  2. O. B. Litvinov, Technology of Synthetic Rubbers (Chem. Press, 1950).

  3. F. R. Mayo, F. M. Lewis and W. Hulse, J. Am. Chem. Soc. 70, 4, 1523 (1948).

    Google Scholar 

  4. L. B. Trukhmanova, Candidate's Thesis (Institute of Macromolecular Compounds, Leningrad, 1954).

  5. K. W. Doak and D. L. Dieneen, J. Am. Chem. Soc. 73, 1084 (1951).

    Google Scholar 

  6. F. C. Foster, J. Polymer Sci. 5, 3, 363 (1950).

    Google Scholar 

  7. M. F. Shostakovsky and L. M. Khomutov, Bull. Acad. Sci. USSR, Div. Chem. Sci. 1955, 133(T.p. 115).

    Google Scholar 

  8. C. Schildknecht, Vinyl Ethers; Monomers; Collection of papers (Foreign Lit. Press, Moscow, 1953).

    Google Scholar 

  9. M. F. Shostakovsky, Vinyl Ethers (Acad. Sci. USSR Press, 1952).

  10. W. H. Shearon, I. P. McKenzie and M. E. Samuels, Ind. Eng. Chem. 40, 769 (1948.

    Google Scholar 

  11. J. Williams and H. W. Walker, Ind. Eng. Chem. 25, 199 (1933).

    Google Scholar 

  12. S. N. Ushakov, S. P. Mitsengendler, and B. N. Polyatskina, J. Appl. Chem. 23, 512 (1950) (T.p. 535).

    Google Scholar 

  13. S. N. Ushakov, S. P. Mitsengendler, and V. A. Chekhovskaya, J. Appl. Chem. 24, 485 (1951)(T.p. 529).

    Google Scholar 

  14. W. G. Barb, J. Polymer Sci. 11, 117 (1953).

    Google Scholar 

  15. G. E. Ham, J. Polymer Sci. 14, 87 (1954).

    Google Scholar 

  16. W. Chalmers, Can. J. Research 7, 4, 472 (1932).

    Google Scholar 

  17. E. I. Barg, Technology of Plastics (State Chem. Press, Leningrad, 1954), p. 291.

    Google Scholar 

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Mitsengendler, S.P., Krasulina, V.N. & Trukhinanova, L.B. Copolymerization of dienic hydrocarbons with vinyl ethers. Russ Chem Bull 5, 1137–1145 (1956). https://doi.org/10.1007/BF01177367

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  • DOI: https://doi.org/10.1007/BF01177367

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