Skip to main content
Log in

Synthesis of SBS thermoplastic block copolymers in cyclohexane in the presence of diethylether used as a structure modifier

  • Published:
Journal of Polymer Research Aims and scope Submit manuscript

Abstract

Diethylether (DEE) was used as a structure modifier during the synthesis of linear styrene-butadiene block copolymers of poly A-block-polyB-block-polyA type (SBS). The microstructures of synthesized polymers were analyzed, and the effect of DEE on polymerization kinetics was studied. Addition of DEE at 2 wt% concentration results in the highest styrene polymerization rate, while addition at 6 wt% concentration gives the highest butadiene polymerization rate. The vinyl content of the polybutadiene portion increases from 14 to 47% with an increase in the DEE concentration from 500 ppm to 10 wt% while thetrans- l,4 andcis-1,4 isomers decrease. For SBS polymer synthesized via a sequential method, the addition of DEE as a structure modifier minimizes the crossover deficiency which would otherwise result in a skewed molecular weight distribution with a higher polydispersity. For SBS polymers made via a coupling method, the coupling efficiency appears to be constant in a range of DEE concentration from 500 ppm to 1 wt% before declining with a further increase in DEE.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. M. M. Wald and M. G. Quam, U.S. Pat. 3,700,633 (1972).

  2. S. Davison and W. P. Gergen, U.S. Pat. 4,041,103 (1977).

  3. Y. Kishimoto and H. Morita, U.S. Pat. 4,501,857 (1985).

  4. F. W. Stavely,Ind. Eng. Chem. 48, 778 (1956).

    Google Scholar 

  5. A. V. Tobolsky and C. E. Rogers,J. Polym. Sci.,40, 73 (1971).

    Google Scholar 

  6. M. Morton and L. J. Fetters,Rubber Chem. Technol.,48, 359 (1975).

    Google Scholar 

  7. S. Bywater and D. J. Worsfold,Can. J. Chem.,40, 1565 (1962).

    Google Scholar 

  8. F. Schue, D. J. Worsfold and S. Bywater,Macromolecules,3, 509 (1970).

    Google Scholar 

  9. D. J. Worsfold and S. Bywater,Can. J. Chem.,42, 2884 (1964).

    Google Scholar 

  10. E. R. Santee and R. Chang, Jr.; M. Morton,J. Polym. Sci., Polum. Lett., Ed.,11, 449 (1973).

    Google Scholar 

  11. M. Morton, R. D. Standerson and R. Sakata,J. Polym. Sci., Part B,9, 61 (1971).

    Google Scholar 

  12. M. Morton, R. D. Standerson and R. Sakata,Macromolecules,6, 181 (1973).

    Google Scholar 

  13. M. Morton,Anionic Polymerization: Principles and Practice, Academic Press, 1983.

  14. R. N. Young, R. P. Quirk and L. J. Fetters,Advances in Polymer Science,56,Anionic Polymerization, Springer-Verlag, 1984.

  15. P. Rempp, P. Lutz and E. Franta,J. Macro. Sci., Pure Appl. Chem.,A31, 891 (1994).

    Google Scholar 

  16. R. P. Hampton,Anal. Chem.,21, 923 (1949).

    Google Scholar 

  17. J. L. Binder,Anal. Chem.,26, 1877 (1954).

    Google Scholar 

  18. V. D. Mochol,Rubber Chem. Technol.,54, 685 (1967).

    Google Scholar 

  19. F. Conti, M. Delfini and A. L Serge,Polymer,18, 310 (1977).

    Google Scholar 

  20. Y. Tanaka, H. Sato, K. Miyashita,Rubber Chem. Technol.,54, 685 (1981).

    Google Scholar 

  21. A. L. Segre, M. Delfini, F. Conti and A. Boicelli,Polymer,16, 338 (1975).

    Google Scholar 

  22. F. Conti, M. Delfini and A. L. Segre,Polymer,15, 539 (1974).

    Google Scholar 

  23. D. Werstler,Rubber Chem. Technol.,53, 1191 (1980).

    Google Scholar 

  24. J. C. Randall,J. Polymer Sci., Polymer Phys. Ed.,15, 1451 (1977).

    Google Scholar 

  25. R. Petiaud and H. Waton,Proton & Carbon NMR Spectron of Polymers, Quang Tho Pham., CNRS-SERVICE Central d'Analyse-Lyon France & Marie-France Llauro-Durricades CNRS-SERVICE des Materiaux Organiques-Lyon. France, 1991.

    Google Scholar 

  26. R. M. Silverstein, G. C. Bassler, Morril,Spectrometer Identifcation of Organic Compounds, 5th Ed., Wiley, New York, 1991.

    Google Scholar 

  27. M. Morton and F. R. Ells,J. Polym. Sci.,61, 25 (1962).

    Google Scholar 

  28. M. Morton, J. E. McGrath and P. C. Juliano,J. Polym. Sci.,C26, 99 (1969).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Huang, DC., Lin, YC. & Tsiang, R.CC. Synthesis of SBS thermoplastic block copolymers in cyclohexane in the presence of diethylether used as a structure modifier. J Polym Res 2, 91–98 (1995). https://doi.org/10.1007/BF01493208

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01493208

Keywords

Navigation