TLCP phase

Therefore, we can conclude that there exists an optimum amount of compatibilizer for the best dispersion of TLCP phase and for the most improvement of the in situ composites with high fibrillation. Excess amounts of PEsI coalesce the TLCP droplets. The adhesion at the... 

Figure 11 Polarized microscope photographs ( x 800) (A) PBT-TLCP-elastomer blend (60 25 15 wt ratio). Dark phase is the TLCP phase. (B) Nylon 6-TLCP-elastomer blend (60 25 15 wt ratio). Dark phase is the TLCP phase and large white one is the elastomer phase. Source Ref. 56.

As shown in Fig. IIB, dispersion morphology for the nylon 6/Vectra B/SA-g-EPDM blend was totally different from that of the PBT-Vectra A-SA-g-EPDM blend. TLCP phases were very uniformly and finely dispersed in the nylon 6-Vectra B-SA-g-EPDM blend and a large fibril shape observed in the PBT-Vectra A-SA-g-EPDM blend could not be seen under polarized microscope. It should be noted that the size of the dispersed TLCP phase is very small (submicron size). This small size of the TLCP phase in the nylon 6/elastomer matrix was not observed by any others [4,54,55,58]. A closer look by SEM more clearly revealed the dispersion of Vectra B in the matrix (Fig. 12B). TLCP phases are very... 

With respect to good adhesion, reduced interfacial tension, fine distribution of TLCP phase, and the use of a compatibilizer can be very effective for this purpose. Remarkably improved mechanical properties (good impact properties as well as tensile properties) can be obtained with optimum amounts of the compatibilizer. Excess amounts of the compatibilizer causes the emulsifying effect to coalesce the dispersed TLCP... 

Strong elongational deformation and use of matrix polymers whose viscosity is higher than that of TLCP phase are better to ensure uniform and fine fibril formation. But application of compatibilizing techniques to in situ composite preparation can be useful to get the most desirable products. These can reduce the high costs of the liquid crystalline polymers and expensive special engineering plastics used for the in situ composite preparation and reduce the processing cost, whereas they can increase the performance of produced in situ composites, hence, their applications, too. 

As demonstrated, Eq. (7) gives complete information on how the weight fraction influences the blend viscosity by taking into account the critical stress ratio A, the viscosity ratio 8, and a parameter K, which involves the influences of the phenomenological interface slip factor a or ao, the interlayer number m, and the d/Ro ratio. It was also assumed in introducing this function that (1) the TLCP phase is well dispersed, fibrillated, aligned, and just forms one interlayer (2) there is no elastic effect (3) there is no phase inversion of any kind (4) A < 1.0 and (5) a steady-state capillary flow under a constant pressure or a constant wall shear stress. 

Figure 7.3 The deformation scheme of a dispersed TLCP phase in the compatibilized in situ composites [46].

---