Blends of thermotropic liquid crystalline polymer (LCP) and polyphenylene s
ulfide(PPS) were studied over the entire composition range using Rheometric
s Stress Rheometer, capillary rheometer, and differential scanning calorime
ter. There is no molecular scale mixing or chemical reaction between the co
mponents, as evidenced by melting and crystallization points, in the PPS ph
ase. From the strain scaling transients test at low-rate, LOP and the blend
s require approximately 60 strain units to obtain steady state shearing res
ults. The large recoveries in the strain recovery test, magnitude 3 to 3.3,
strain unit, are likely the results of texture present in LCPs. With incre
asing PPS content in LCP/PPS blends, the total recovery declines. Scaling o
f the transient strain rate remains, but the magnitude of the transients is
reduced. At low-rate, when the LCP is added, to the PPS, the pure melts ha
ve similar viscosity: 500 Pa . s for LCP and 600 Pa . s for PPS, but the vi
scosity of the blends goes through a maximum with concentration that is nea
rly three times the viscosity of the individual melts. At high-rate, a sign
ificant depression of the viscosity is observed in the PPS-rich composition
s and this may he due to the fibrous, structure of the LOP at high shear ra
tes.