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.
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References
M. M. Wald and M. G. Quam, U.S. Pat. 3,700,633 (1972).
S. Davison and W. P. Gergen, U.S. Pat. 4,041,103 (1977).
Y. Kishimoto and H. Morita, U.S. Pat. 4,501,857 (1985).
F. W. Stavely,Ind. Eng. Chem. 48, 778 (1956).
A. V. Tobolsky and C. E. Rogers,J. Polym. Sci.,40, 73 (1971).
M. Morton and L. J. Fetters,Rubber Chem. Technol.,48, 359 (1975).
S. Bywater and D. J. Worsfold,Can. J. Chem.,40, 1565 (1962).
F. Schue, D. J. Worsfold and S. Bywater,Macromolecules,3, 509 (1970).
D. J. Worsfold and S. Bywater,Can. J. Chem.,42, 2884 (1964).
E. R. Santee and R. Chang, Jr.; M. Morton,J. Polym. Sci., Polum. Lett., Ed.,11, 449 (1973).
M. Morton, R. D. Standerson and R. Sakata,J. Polym. Sci., Part B,9, 61 (1971).
M. Morton, R. D. Standerson and R. Sakata,Macromolecules,6, 181 (1973).
M. Morton,Anionic Polymerization: Principles and Practice, Academic Press, 1983.
R. N. Young, R. P. Quirk and L. J. Fetters,Advances in Polymer Science,56,Anionic Polymerization, Springer-Verlag, 1984.
P. Rempp, P. Lutz and E. Franta,J. Macro. Sci., Pure Appl. Chem.,A31, 891 (1994).
R. P. Hampton,Anal. Chem.,21, 923 (1949).
J. L. Binder,Anal. Chem.,26, 1877 (1954).
V. D. Mochol,Rubber Chem. Technol.,54, 685 (1967).
F. Conti, M. Delfini and A. L Serge,Polymer,18, 310 (1977).
Y. Tanaka, H. Sato, K. Miyashita,Rubber Chem. Technol.,54, 685 (1981).
A. L. Segre, M. Delfini, F. Conti and A. Boicelli,Polymer,16, 338 (1975).
F. Conti, M. Delfini and A. L. Segre,Polymer,15, 539 (1974).
D. Werstler,Rubber Chem. Technol.,53, 1191 (1980).
J. C. Randall,J. Polymer Sci., Polymer Phys. Ed.,15, 1451 (1977).
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.
R. M. Silverstein, G. C. Bassler, Morril,Spectrometer Identifcation of Organic Compounds, 5th Ed., Wiley, New York, 1991.
M. Morton and F. R. Ells,J. Polym. Sci.,61, 25 (1962).
M. Morton, J. E. McGrath and P. C. Juliano,J. Polym. Sci.,C26, 99 (1969).
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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
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DOI: https://doi.org/10.1007/BF01493208