Abstract
AbstractRare earth oxide, neodymium oxide (Nd2O3), ‐assisted melt free‐radical grafting of maleic anhydride (MAH) on isotactic‐polypropylene (i‐PP) was carried out by reactive extrusion. The experimental results reveal that the addition of Nd2O3 into reactive system leads to an enhancement of the grafting degree of MAH, along with an elevated degradation of i‐PP matrix. When Nd2O3 content is 4.5 mmol %, the increment of the grafting degree of MAH (maximally) is up to about 30% compared with that of the related system without adding Nd2O3, while the severest degradation of i‐PP matrix simultaneously occurs. On the basis of the reaction mechanism of PP‐g‐MAH proposed before, the sequence of β‐scission and grafting reaction is discussed in detail. It is found that, for the reactive system studied, most tertiary macroradicals first undergo β‐scission, and then, grafting reaction with MAH takes place at the new radical chain ends. The imported Nd2O3 has no effect on the aforementioned reaction mechanism, whereas it enhances the initiating efficiency of the initiator, dicumyl peroxide (DCP). We tentatively explain the experimental results by means of synergistic effect between DCP and Nd2O3. It is calculated that the synergistic effect is maximal when the molar ratio of DCP to Nd2O3 is approximately 1:6. © 2005 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 44: 134–142, 2006
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Journal of Polymer Science Part B: Polymer Physics
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.