Methods of processing polypropylene (PP)/ liquid crystalline polymer blends to obtain high mechanical properties from injection molded samples were investigated in this dissertation. Three liquid crystalline polymers (LCPs), two liquid crystalline (LC) copolyesters and one LC poly(ester-amide), were used. The PP/LCP blends were compatibilized with a maleic anhydride grafted polypropylene (MAP) to enhance the mechanical properties. The effect of increasing MAP content on the mechanical properties, morphology, and interfacial tension of injection molded tensile bars and plaques made from blends with 30 wt% LCP was investigated. It was determined that MAP enhances both the tensile strength and modulus, but the tensile strength is increased to a greater degree than the tensile modulus. For the LC copolyesters, the tensile strength appeared to reach a maximum while for the LC poly(ester-amide) the tensile strength increased without limit in the range of MAP contents studied. Simultaneously, a finer dispersion was created as the MAP content was increased. Calculation of the interfacial tension from contact angle measurements indicated that the interfacial tension decreased as MAP was added to the PP matrix. Analysis of the MAP concentration after blending indicated that MAP did not react with the LCP, but enhanced tensile properties resulted from physical interaction such as hydrogen bonding. This mechanism is consistent with the greater property improvements found in the LC poly(ester-amide) blends where the amide group is expected to undergo stronger hydrogen bonding than the ester group.

Analysis of the injection molding of these blends found that heat transfer and solidification significantly affected the flexural modulus of these blends. Injection molding conditions such as fill time, mold thickness, mold temperature and melt temperature were investigated in three molds of different thicknesses. Different processing relationships were found between the LC copolyesters and the LC poly(ester-amide). For the former LCP blends, the highest moduli were obtained from the thinnest mold in a manner parallel to that of the moduli of neat LCPs. For the latter LCP blends, the highest moduli were obtained in the intermediate thickness mold. The differences between the copolyester and LC poly(ester-amide)s processing / property relationships were related to the melt rheology of the LCPs. For the LC copolyesters, maximum mechanical properties were obtained when the melt temperature was selected so that the storage and loss moduli of the LCP were nearly equal. This equality of storage and loss moduli could not be achieved with the LC poly(ester-amide). In addition, upon cooling, the storage and loss moduli of the LC poly(ester-amide) indicated that rapid solidification occurred while a much lower rate of solidification was indicated for the LC copolyesters. In addition the mechanical properties were sensitive to the rate of cooling as indicated by the Graetz number. It was speculated that attainment of the highest mechanical properties was related to the LCP being deformed during the filling stage followed by rapid solidification of the LCP morphology upon cessation of flow.