Abstract

Abstract A basic investigation of the development of crystallization and orientation during the melt spinning of syndiotactic and isotactic polypropylene is described. Both polymers were melt spun through ambient air or into ice water at various draw-down ratios and melt temperatures. The melt spun filaments were characterized by wide angle x-ray diffraction (WAXD), birefringence and differential scanning calorimetry (DSC). The polymorphic behavior of isotactic polypropylene during melt spinning is well known. The filaments melt spun through ambient air exhibit the monoclinic α-form while the filaments melt spun into ice water form a smectic structure at low draw-down ratios. Syndiotactic polypropylene also exhibited polymorphic behavior during melt spinning. Disordered Form I with (t2g2)2 helices was found at low spinline stresses and Form III with all trans chain conformation was found at high spinline stresses. The criterion of the spinline stress for this transition was found to be about 6–9 MPa for all samples of various molecular weights, melt temperatures and cooling rates. Syndiotactic polypropylene crystallized much more slowly than isotactic polypropylene and did not exhibit a smectic mesomorphism under ice-water quenched conditions. The melt spun filaments of syndiotactic polypropylene exhibited lower birefringences and amorphous orientations but higher crystalline orientations than those of isotactic polypropylene, compared at the same spinline stresses.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.