The intrinsic hydrophobic character of polypropylene limits its performance in many porous membrane applications. This can be improved by hydrophilic modification of the film surface through blending with hydrophilic polymers. For producing the precursor films and, consequently, microporous membranes with the appropriate crystalline lamellar morphology, the polypropylene chains should preserve their elongated form to serve as initial nuclei for the later development of lamellar crystals. The relaxation time of the chains is the most important factor for this stage. Commercial maleic anhydride and acrylic acid grafted polypropylenes were melt blended with a polypropylene at different weight ratios. The results showed that the modifiers lowered the crystalline orientation of the blends as compared to neat polypropylene films. The effect of the modifier on the melt relaxation spectra of the blends was investigated, and a linear relationship was found between the characteristic relaxation time of the blends and their crystalline orientation function.