Rheological investigation of microphase separation transition of polyurethane elastomer

• Published in: Journal of applied polymer science 2007-02, Vol.103 (4), p.2107-2112
• Main Authors: Yang, I-Kuan, Wang, Pei Ju, Tsai, Ping Hung
• Format: Article
• Language: English
• Subjects: Applied sciences; atomic force microscopy (AFM); Exact sciences and technology; microphase separation; Organic polymers; Physicochemistry of polymers; polyurethane; Properties and characterization; rheology; Thermal and thermodynamic properties; viscoelastic properties
• ISSN: 0021-8995; 1097-4628
• DOI: 10.1002/app.24641

A technique of linear viscoelasticity measurements coupling with temperature scanning was found effective in the detection of microphase separation transition (MST) and in the determination of MST temperature. The validity and accuracy of the technique were confirmed and reinforced by atomic force microscopy and differential scanning calorimetry (DSC). The technique was applied to a study of the MST of a series of 13 polyurethane (PU) elastomers based on mixed toluene diisocyanate (TDI), 1,4 butadiol, and poly(tetramethylene oxide) (PTMO) of two different molecular weights; the MST temperatures of the PU elastomer samples were measured. Although each of the 13 polymer samples had distinct hard segment content and used PTMO of different chain lengths, or mixed PTMO, the MST temperatures of the 13 samples formed a linear master curve when the MST temperature was plotted against the fraction of hard segment. The master curve indicated that the MST temperature is independent of the length and type of PTMO. It was also found that 2,4 TDI prevailing over its isomer 2,6 TDI played a dominant role in the MST of this series of PU elastomers. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 103: 2107–2112, 2007