ABSTRACT:The effects of addition of the 3rd component of thermotropic liquid crystal polymer (TLCP) on the mechanical properties and structure ofVectra A-reinforced polycarbonate (PC) were studied. The 3rd TLCP was the copolymer of p-hydroxybenzoate (PHB) and ethyleneterephthalate, known as X-7G TLCP. PC, Vectra A, and a small amount of the 3rd TLCP were blended in the molten state, the extrudate of which was cut and injection-molded. The mechanical properties of the blends were improved dramatically by addition of a small amount of the 3rd TLCP component. SEM revealed that the blend systems were always phase-separated, even after injection-molded, and the fibrils of Vectra A in the injection-molded blends became finer and longer in the presence of the 3rd TLCP. FT-IR indicated that no special chemical reaction took place between the TLCP and PC. The dynamic viscoelastic analysis indicated that the addition of the 3rd TLCP component had almost no effect on the thermal endurance of the blends. X-Ray diffraction analysis showed that the orientation ofVectra A fibril in the blend became higher when the 3rd TLCP was added, which Jed to the great improvement of the mechanical properties. Based on the assumption of additivity law, the fibril modulus was evaluated and found to be in the same order as the orientation evaluation by X-ray diffraction. The thinning of fibrils by addition of the 3rd TLCP component was discussed based on the crystallization kinetics of rodlike molecules.KEY WORDS Polycarbonate/ Liquid Crystal/ Ternary Blends/ Mechanical Properties / Morphology / Crystallization Kinetics / As one of the applications of the thermotropic liquid crystal polymers (TLCP), the blends of engineering plastics and TLCP are promising the improvement of mechanical and thermal properties due to the reinforcing function and thermal endurance of TLCP. There have been many engineering and scientific reports on this subject. Kiss 1 suggested a concept of"in situ composite," emphasizing the fact that the TLCP reinforcement could be formed "in situ" during processing. Isayev et al. 2 called them as "self-reinforced melt processable polymer composite". According to Brostow et al. 3 the composite could be classified into two kinds: one was the traditional fiber-reinforced composite, being classified as a heterogenous composite; the other was the molecular composite, such as selfreinforced plastics and the molecular composite in the strict meaning suggested by Takayanagi. 4 From many papers reported on the blends of the engineering plastics and TLCP, one can find two important facts: such blend systems are usually phase-separated and