4.5 Article

c-perpendicular orientation in thin nanoporous-crystalline poly (2,6-dimethyl-1,4-phenylene)oxide films

期刊

POLYMERS FOR ADVANCED TECHNOLOGIES
卷 33, 期 7, 页码 2344-2351

出版社

WILEY
DOI: 10.1002/pat.5690

关键词

guest-induced crystallization; nanoporous-crystalline alpha form; planar orientation; poly (2,6-dimethyl-1,4-phenylene)oxide; thin films

资金

  1. Italian Ministry of Education, University and Research (MIUR)
  2. Ministry of Education, University and Research

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Four different preparation methods for nanoporous-crystalline films of PPO with high crystallinity and high c-perpendicular orientation, even for thickness as low as 5 μm, are described in this paper. The results support the hypothesis that the c-perpendicular orientation is due to the formation of flat-on crystalline lamellae through nanoconfined co-crystallization of PPO. An anomalous temperature dependence of c-perpendicular orientation for limonene-induced co-crystallization with PPO is also explained.
Nanoporous-crystalline films of poly(2,6-dimethyl-1,4-phenylene)oxide (PPO), exhibiting c-perpendicular orientation (c(perpendicular to)) orientation (i.e., the orientation of the crystalline chain axes being preferentially perpendicular to the film plane), show the advantage of faster guest diffusivity and higher transparency. However, by using the methods described in the literature, this perpendicular orientation cannot be achieved for low thickness films (<= 20 mu m). In this paper, we describe four different preparation methods, which are suitable to get high degree of crystallinity (X-c >40%) as well as high degree of c(perpendicular to) orientation (-0.5< f(c) <- 0.3) of CC and NC alpha forms, for film thickness even as low as 5 mu m. All the described methods are based on reduction of guest sorption kinetics. The reported results also confirm our previous hypothesis that c(perpendicular to) orientation is due to formation of flat-on crystalline lamellae, which in turn are due to nanoconfined co-crystallization of PPO. An anomalous temperature dependence of c(perpendicular to) orientation for limonene-induced co-crystallization with PPO is described and rationalized.

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