In this study, poly(L-lactide) (PLA) is melt-blended with thermoplastic polyurethane (TPU) to modify the brittleness of PLA. An aliphatic ester-based TPU was selected in order to have an ester sensitivity for degradation and an inherent biocompatibility. Using this compatible TPU, there was no need to apply problematic compatibilizers, so the main positive properties of PLA such as biocompatibility and degradability were not challenged. The detected microstructure of PLA/TPU blends showed that when the TPU content was lower than 25 wt %, the structure appeared as sea-islands, but when the TPU content was increased, the morphology was converted to a cocontinuous microstructure. A higher interfacial surface area in the blend with 25 wt % TPU (PLA25) resulted in a higher toughness and abrasion resistance. The various analyses confirmed interactions and successful coupling of two phases and confirmed that melt-blending of PLA with the aliphatic ester-based TPU is a convenient, cost-effective, and efficient method to conquer the brittleness of PLA. The prepared blends are general-purpose plastics, but PLA25 showed an optimum mechanical strength, toughness, and biocompatibility suitable for a wide range of applications.
Oscillations superimposed on steady shear flows have been used repeatedly in the past to determine the relaxation modes in flowing associative polymers. In these experiments, the oscillatory motion has been parallel to the steady-state flow. Here, parallel superposition moduli on associative polymers will be compared with superposition experiments in which the oscillatory motion is perpendicular to the steady-state flow. In the latter experiments, there is less interference between the steady flow and the superimposed oscillations, which has drastic consequences for the results. Data are shown for a HASE polymer (hydrophobic alkali-swellable emulsion). As in other fluids, the limiting viscosities at zero frequency differ drastically, and negative storage moduli can be obtained in parallel superposition. The apparent relaxation frequencies during flow, as derived from parallel superposition measurements, are an order of magnitude smaller than those derived from orthogonal superposition. The effect of shear rate on the average relaxation times seems to be qualitatively similar in the two superposition modes, but the moduli-frequency curves differ in shape. The shapes of these curves also reflect the associative nature of the polymers.
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