期刊
MACROMOLECULES
卷 47, 期 2, 页码 571-581出版社
AMER CHEMICAL SOC
DOI: 10.1021/ma402328k
关键词
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资金
- Penn State University through a Multidisciplinary University Research Initiative (MURI) grant from the Office of Naval Research [N00014-10-1-0944]
This paper discusses the synthesis of a new family of well-controlled isotactic polypropylene ionomers (iPP-NH3+Cl-) containing up to 5 mol % of NH3+Cl- ionic groups, with high molecular weight and narrow molecular weight and composition distributions, as well as good processability in melt and solution. A systematic study was conducted using various isospecific Ziegler-Natta and metallocene catalysts in the copolymerization of propylene and a high a-olefin comonomer containing a silane-protected amino group and the subsequent work-up procedures that can prevent undesirable side reactions in forming iPP-NH3+Cl- ionomers in a one-pot process. The resulting copolymers were carefully monitored by polymer solubility and a combination NMR, GPC-triple detectors, DSC, and mechanical property measurements. Evidently, the most suitable reaction process requires a combination of the rac-Me2Si[2-Me-4-Ph(Ind)](2)ZrCl2 metallocene catalyst system with a purified d-MAO (TMA-free), 6-bis(trimethylsilyl)amino-1-hexene comonomer during the copolymerization reaction and a work-up procedure to directly interconvert the silane-protected amino groups (-N(SiMe3)(2)) into -NH3+Cl- ionic groups before exposing to air. The attempt of isolating both iPP-N(SiMe3)(2) and iPP-NH2 intermediates resulted in the insoluble (cross-linked) products. On the other hand, the resulting iPP-NH3+Cl- ionomers were melt processed in air and showed a systematic increase of mechanical properties and high-temperature stability with the increase of NH3+Cl- content.
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