Abstract
We have studied by small-angle neutron scattering (SANS) the crystallization of syndiotactic polypropylene (sPP) homopolymer in dilute hydrocarbon solution in parallel with the self-assembling behavior of crystalline−amorphous block copolymers of (syndiotactic propylene)-block-poly(ethylene-co-propylene) [sPP−P(E-co-P)] and atactic−isotactic multiblock polypropylene copolymers (aPP−iPP). Homopolymers and diblock copolymers of various molecular weights and volume fractions were investigated in decane over a wide temperature range (between 160 and −20 °C) while the temperature evolution of the aPP−iPP aggregates was studied in dodecane starting from 175 °C. The homopolymer crystallizes by forming platelets of a thickness of about 60−65 Å, independent of the molecular weight or polymer volume fraction in solution. The diblock copolymers aggregate by forming a complex morphology that shows a multilevel structure. This was investigated with SANS and ultra-SANS (USANS) over 3 orders of magnitude in size scale. At small scale (tens of angstroms) an overall 2-dimensional structure seems to be formed. It evolves at intermediate scale (hundreds of angstroms) into a rodlike structure. The rods associate in bundles that at a micrometric scale form supramolecular structures like networks. Such an association could be promoted by the PE sequences present within the P(E-co-P) block. The multiblock copolymer forms very open rodlike aggregates and demonstrates that the general morphology of self-assembling materials with multiple alternating crystalline−amorphous blocks appears to be 1-dimensional.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
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.