Belov Nikolay A, Alentiev Aleksandr Yu, Pashkevich Dmitrii S, Voroshilov Fedor A, Dvilis Edgar S, Nikiforov Roman Yu, Chirkov Sergey V, Syrtsova Daria A, Kostina Julia V, Ponomarev Igor I, Asanov Igor P, Bogdanova Yulia G
Engineering Center, Tomsk Polytechnic University, 30, Lenin Avenue, 634050 Tomsk, Russia.
A.V. Topchiev Institute of Petrochemical Synthesis, Russian Academy of Sciences, 29, Leninskii Prospect, 119991 Moscow, Russia.
Polymers (Basel). 2022 Nov 26;14(23):5152. doi: 10.3390/polym14235152.
A direct fluorination technique was applied for the surface treatment of PIM-1 films in a liquid phase (perfluorodecalin). The fluorinated samples were analyzed by various instrumental techniques. ATR-IR spectroscopy showed that the fluorination predominantly takes place in methylene- and methyl-groups. Cyano-groups, aromatic hydrogens and the aromatic structure of the PIM-1 repeat unit were shown to be relatively stable at the fluorination conditions. XPS confirmed that the concentration of fluorine, as well as oxygen, in the near surface layer (1 nm) increases with fluorination time. C1s and O1s surface spectra of the fluorinated PIM-1 samples indicated an appearance of newly-formed C-F and C-O functional groups. Scanning electron microscopy and X-ray energy-dispersive spectroscopy of the fluorinated PIM-1 samples showed an increase of the fluorine concentration at the surface (0.1-1 μm) with the treatment duration. Analysis of the slices of the PIM-1 films demonstrated a decline of the fluorine content within several microns of the film depth. The decline increased with the fluorination time. A model of fluorine concentration dependence on the film depth and treatment duration was suggested. A change in the specific free surface energy as a result of PIM-1 fluorination was revealed. The fluorination time was shown to affect the surface energy (γ), providing its shift from a low value (25 mJ∙m), corresponding to tetrafluoroethylene, up to a relatively high value, corresponding to a hydrophilic surface.
采用直接氟化技术对液相(全氟萘烷)中的PIM-1薄膜进行表面处理。通过各种仪器技术对氟化后的样品进行分析。衰减全反射红外光谱表明,氟化主要发生在亚甲基和甲基基团上。氰基、芳氢以及PIM-1重复单元的芳环结构在氟化条件下显示出相对稳定。X射线光电子能谱证实,近表面层(约1nm)中氟和氧的浓度随氟化时间增加。氟化PIM-1样品的C1s和O1s表面光谱表明出现了新形成的C-F和C-O官能团。氟化PIM-1样品的扫描电子显微镜和X射线能量色散光谱显示,随着处理时间的延长,表面(约0.1-1μm)的氟浓度增加。对PIM-1薄膜切片的分析表明,薄膜深度几微米内的氟含量下降。这种下降随着氟化时间的增加而增大。提出了氟浓度与薄膜深度和处理时间关系的模型。揭示了PIM-1氟化导致的比自由表面能的变化。结果表明,氟化时间会影响表面能(γ),使其从对应于四氟乙烯的低值(25 mJ∙m)转变为对应于亲水性表面的相对高值。