Summary
Computer simulations show that oligomers with two different terminal groups with dissimilar reactivities for isocyanates give a delayed viscosity rise in polyurethanes. This is a desired behaviour for RIM processes. Therefore, an α-hydroxy-ω-amino poly(ethylene oxide) (HAPEO) has been prepared. The synthesis was carried out by the ethoxylation of 2-hydroxyethyl phthalimide as a blocked amine. Hydrazinolysis appears to be the best way to obtain the deblocked oligomer. The product properties were compared with an oligomeric diamine ether (Jeffamine D2000). The gel time of HAPEO (Mn=500) and JAD2000 (Mn=2000) was the same (2 sec.). The product with HAPEO had a higher modulus, a comparable impact and tensile strength and a lower elongation at break.
Similar content being viewed by others
References
K.C.Frisch, Ruber Chem. and Techn. 53, no 1, 126–140, (1980).
C.W.Macosko, Polym. Eng. and Sci., 28, nr 10, 660–669, (may 1988).
B.J.R. Scholtens and G.P.J.M. Tiemersma Thoone, Computer Applications in Applied Polymer Science II: Automation, Modelling and Simulation, T. Provder, Ed., ACS Symposium Series 404, Am. Chem. Soc., Washington, DC, 1989, ch. 19, p. 213; G.P.J.M. Tiemersma-Thoone, B.J.R. Scholtens, K. Dusek and M. Gordon, J. Polym. Sci. Part B, Polym. Phys., 29, 463–482, (1991).
K.C.Frisch, Advances in Urethane Sci. and Techn., vol 1, 1–30, (1971).
J.H.Billman, J. Am. Chem. Soc. 65, 761–762, (1943).
Methoden der Organischen Chemie, Stickstoffverbindugen II, 4e Auflage, Ed. Houben Weil.
S. Wolfe, Can. J. Chem., 48, no 22, 3572–99.
H.R. Ing, J. Chem. Soc., 1926, 2348–51.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Loontiens, T.J.A., Scholtens, B.J.R., Belt, W.J.W. et al. Synthesis of α-hydroxy-ω-amino poly(ethylene oxide) and its use in reaction injection moulding (RIM). Polymer Bulletin 30, 489–494 (1993). https://doi.org/10.1007/BF00296465
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00296465