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Ultrathin Films from Fluorine Containing Polymers: Fabrication and Characterization
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2002
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EngineeringPolymer NanotechnologyChemistryUltrathin FilmsReaction TimePolymersChemical EngineeringPolymer MaterialPolymer TechnologyHybrid MaterialsPolymer ChemistryMaterials ScienceLb FilmsPolymer EngineeringSurface ModificationPolymer AnalysisPolymer ScienceConjugated PolymerThin FilmsFunctional Materials
Monolayers and ultrathin films of some fluorine containing polymers were prepared by the Langmuir-Blodgett (LB) technique. The polymers were obtained using two main synthetic approaches: firstly, polyamide (PA-1) and polyimide (PI-1) were prepared from direct polycondensation of 4,4′-hexafluoroisopropylidenediphthalic anhydride and 4,4′-hexafluoroisopropylidenedianiline in N-methyl-2-pyrrolidone (NMP). The thermogravimetric analysis (TGA) for PI-1 yielded 580°C by 1% weight loss. They formed stable monolayers with a collapse pressure of 62 mN/m and a collapse area of 0.20 nm2 per repeat unit (R.U.) in the case of PA-1, for PI-1 the collapse pressure was 60 mN/m associated with a collapse area of 0.23 nm2 per R.U. Secondly, poly[(maleic acid perfluorooctylamide-imide)-co-ethylene] (PAPE) with fluorinated side chains was synthesized from poly[(maleic anhydride)-co-ethylene]. They formed stable monolayers too. Multilayer depositions onto various substrates were possible for all the synthesized polymers. LB films were characterized by ultra-violet/visible spectroscopy (UV-Vis), surface plasmon resonance (SPR), dielectric spectroscopy and atomic force microscopy (AFM). Gas phase polymerization of tetrafluoropropyl methacrylate (TFPM) was carried out in the presence of macroinitiator, poly[octadecene-co-(maleic anhydride)] modified with tert-butyl hydroperoxide. Film thickness could be controlled on different hydrophobic substrates varying the reaction time.