Segmented thermoplastic polyurethanes (PUs) were synthetized using macrodiols with different functional groups (carbonate, ester, and /or ether) as a segment with a molar mass of 1000 and 2000 g/mol, and 4,4’-diphenylmethane diisocyanate (MDI) and 1,4-butanediol as a rigid segment. The polyurethanes obtained reveal a wide variation of microphase separation degree that is correlated with mechanical properties and retention of tensile properties under degradation by heat, oil, weather, and water. Different techniques such as differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), Fourier transform infrared (FTIR), and synchrotron small-angle X-ray scattering (SAXS) were used to determine rigid-flexible segments’ phase behaviour. Retention of tensile properties determines the stability of the samples under different external factors. This work reveals that pure polycarbonate-based macrodiols induce the highest degree of phase miscibility, better tensile properties, hardness shore A, and retention of tensile properties under external agents.
Segmented thermoplastic polyurethanes (PUs) were prepared from 4,4 0 -diphenylmethane diisocyanate (MDI), 1,4-butanediol (BD) and different macrodiols with a molar mass of 1000. Properties of those PUs based on polycarbonatediol (PCD) were compared with their homologous based on polyesterdiol and polyetherdiol as macrodiols. The proportion used in this study was macrodiol:BD:MDI ¼ 1:2:3, in mole ratio. The hard segment weight percentage is 48 wt% for different PUs. Thermogravimetric analysis, differential scanning calorimetry, differential mechanical analysis, Fourier transform infrared-attenuated total reflection spectroscopy, as well as mechanical properties and retention on flexural properties tests were employed to characterize the physicochemical, thermal and mechanical properties of different PUs. Comparison of PUs based on PCD, ester and ether macrodiols indicates a better miscibility, higher hard segment-soft segment interactions and durability for the ones based on PCD. It is especially noticeable that the transparency of the films obtained with PCD as macrodiols as well as their good tensile strength and performance to standard durability tests, in comparison with those based on polyester and polyether. This trend could be related with a better miscibility caused by the highest hard segment-soft segment interactions favored by the presence of the carbonate groups.
Segmented thermoplastic polyurethanes (PUs) have been synthesized with polycarbonate diol as soft segment and 4,4 0diphenylmethane diisocyanate and butanediol as hard segment. Two different series employing two different soft-segment molar mass, 1000 and 2000 g/mol, and by changing the hard-segment content from 32 to 67% have been investigated with the aim to elucidate the effect of the different content variations on the properties. Morphological, thermal, and mechanical properties have been studied by Fourier transform infrared spectroscopy (FTIR), differential scanning calorimetry (DSC), dynamic mechanical analysis (DMA), wide angle X-ray diffraction, atomic force microscopy, tensile and tear strength, hardness, and specific gravity tests. Properties have been explained from the standpoint of miscibility between hard-and soft-segment microdomains of the tailored segmented PUs through an exhaustive analysis. FTIR, DSC, and DMA measurements revealed that miscibility between hard and soft microdomains increases as the molar mass of the macrodiol decreases. An increase in hard-segment content entailed the formation of larger hard domains with higher crystallinity what results in superior mechanical properties such as higher tensile stress and tear strength, and hardness.
Segmented thermoplastic polyurethanes (PUs) were synthetized using polycarbonate diol as soft segment with a molar mass of 500 and as a hard segment 1,5-pentanediol with a combination of isophorone diisocyanate (IPDI) and hexamethylene diisocyanate (HDI). Differential scanning calorimetry, differential mechanical analysis, Fourier transform infrared-attenuated total reflection spectroscopy, haze, transmittance, hardness, tensile properties and retention of tensile properties tests were employed to characterize the different PUs. The results of this study show that IPDI/HDI relation has a significant impact on the phase mixing, crystallinity and therefore on the PU’s properties. The variation of diisocyanate type ratio allows obtaining PUs of different nature from a high rubbery material with a high content in IPDI to high crystalline PU increasing the HDI content. Material transparency was also modified by decreasing the amorphous nature of the materials with the increase in the HDI content. The weather resistance of the final PU is related with the different isocyanate relation.
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