ABSTRACT:Hydrogen bonds in segmented poly(urethaneurea)s (SPUU) were studied with Fourier transform infrared spectroscopy (FTIR). Absorption curves due to the urethane and urea carbonyl groups were resolved into several peaks by a peak resolving method. Evaluation of individual peak intensity enabled one to estimate the amounts of hydrogen bonds formed with urea and urethane carbonyl groups, referred to as hydrogen bond indices, HvA and HvT• respectively. H vA and H VT were defined as the ratios of absorbances of hydrogen bonded carbonyl groups to free carbonyl groups, respectively for urea (UA) and urethane (UT) carbonyl groups. lt was found that the indices of hydrogen bonds of urethane and urea carbonyl groups were the parameters which represent phase mixing, i.e., dispersion of hard segments in the soft segment matrix, and the cohesive force in the hard segment domain. The variation of the indices of hydrogen bonds with increasing elongation and temperature indicated progress of tlie phase mixing and reduction of the cohesive force of the hard segment domain.KEY WORDS Segmented Poly(urethaneurea) / FTIR / Hydrogen Bond / Phase Mixing / Peak Resolving / Structure, morphology, mechanical and thermal properties, and antithrombogenicity of segmented poly(urethaneurea)s have been studied by many workers because not only for academic interest as multicomponent polymers but also for their industrial applications such as shock absorber, clothes, and medical materials. Most of the characteristic properties ofSPUUs, e.g., high elasticity, durability, antithrombogenicity are due to presence of the microphase separated structure and hydrogen bonds.points of structure and soft and hard segment orientations. The results showed that spherulites were selectively destroyed at the equatorial zone of the spherulite with respect to the stretching direction and then fragmented hard segments were dispersed in the soft segment matrix. Thus, phase mixing occurred. It was also shown that hydrogen bonds play an important role in the structural change in deformation.In previous papers in this series, 1 • 2 the deformation mechanism of segmented poly(urethaneurea)s (SPUUs) during uniaxial stretching and fatigue process were discussed based on deformations of spherulites from the view-* To whom correspondence should be addressed.In the case of SPUUs, the NH groups in the urea or urethane groups and the oxygen of the C = 0 groups in urea, urethane, polyether, or polyester behave as a proton donor and acceptor, respectively. Since hydrogen bonds af-· fect the physical properties, morphology and deformation mechanism of these materials, 895