The crystal morphology and thermal properties of the PA6/PP-g-MAH/POE blends prepared by twin-screw extruder were studied by polarized optical microscopy (POM) and differential scanning calorimetry (DSC) respectively. The results suggest that the crystal morphology of PA6 is acicular crystal while PP-g-MAH is micro-spherulites; The acicular crystals form across POE phase to PA6 phase, and the acicular crystals of PA6 in the POE phase have better regularity in dimension than those in amorphous PA6 phase. Acting as a compatibilizer, PP-g-MAH improves the miscibility of PA6 and POE, leading to the glass transition temperature of the blends decreases gradually with increasing POE contents. PA6 and PP-g-MAH can crystallize individually, and the formed PA6 crystals induced the crystallization of PP-g-MAH at higher temperature; furthermore, PP-g-MAH and POE components can increase the crystallization rate of PA6.

The dynamic mechanical properties, phase morphology and thermal stability of the poly(trimethylene terephthalate)/maleinized poly(octene-ethylene)/organo-montmorillonite nanocomposites (PTT/POE/OMMT) were investigated by using the thermodynamic mechanical analyzer (DMA), transmission electron microscopy (TEM) and thermal gravimetric analyzer (TGA), respectively. The results suggest that the modulus of elasticity of the PTT/POE/OMMT nanocomposite increases, and the glass transition temperature first slightly decreases and then increases with increasing OMMT content because that the TPP plays the role of plasticizer and OMMT plays the role of reinforcing agent. OMMT disperse evenly in the polymer matrix with most of the strip-like sheet morphology. The addition of the OMMT does not apparently affect the thermal stability of the PTT/POE/OMMT nanocomposite.

The rheology, morphology and mechanical properties of the PA6/PP-g-MAH/POE blends prepared by twin-screw extruder were studied by rheometer, scanning electron microscopy, universal tester and impact tester, respectively. The results suggest that the impact strength is improved by the POE acting as a toughening agent, while the compatibility of PA6 and POE is improved by the compatibilizer of PP-g-MAH. Furthermore, the PP-g-MAH component also acts as a reinforcing agent for decreasing the strength depression induced by the POE component. When POE content is about 9 wt% and PP-g-MAH content is about 10% in blends, the blend has the maximum tensile strength and impact strength. All melts of PA6/PP-g-MAH/POE blends are pseudo-plastic fluids. Both the POE and PP-g-MAH components can increase the apparent viscosity of the melt due to their facility of the linear molecular.

A series of poly(trimethylene terephthalate)/maleinized poly(octene-ethylene) copolymer blends are prepared and their melting, crystallization and dynamic mechanical propwerties were studied by using differential scanning calorimetry (DSC) and dynamic mechanical analyzer (DMA) respectively. The results suggest that the glass transition temperature of the blends shift to higher temperature because of the interaction between PTT and POE components. POE-MAH serves as a nucleating agent for the crystallization of PTT, and it increases the crystallizaiton rate of the blend and the start crystallizaiton temperature, but reduces the degree of crystallinity. Proper content of POE, e.g.1-2%, can improve the elastic modulus of the blend, but too much POE will depress the modulus.

In this article, the phase morphology and mechanical properties of poly (trimethylene terephthalate)/maleinized poly (octene-ethylene) copolymer blends are studied by using scanning electron microscopy (SEM), polarized optical microscopy (POM), universal material tester and charpy impact tester. The results suggest that the crystal size of the blends decreases obviously and POE component is partly served as nucleating agent for the crystallization of PTT. PTT and POE have good compatibility in blends because the dispersed phase of POE has even dispersion in blends when POE content is lower than 5%; however, the dispersion state of POE becomes poor when POE content is larger than 5%. The impact strength increases to maximum when the POE content is about 4 %. The tensile strength gets to maximum when POE content is 1-2 %.