Vacuum-ultraviolet photochemically initiated modification of polystyrene surfaces: morphological changes and mechanistic investigations
- Autor: López Gejo, J. / Manoj, N. / Sumalekshmy, S. / Gliemann, H. / Schimmel, T. / Wörner, M. / Braun, M. (2006)
- Quelle: Photochem. Photobiol. Sci. 5 (2006), 948-954
- Datum: 2006
López Gejo, J. / Manoj, N. / Sumalekshmy, S. / Gliemann, H. / Schimmel, T. / Wörner, M. / Braun, M. (2006): „Vacuum-ultraviolet photochemically initiated modification of polystyrene surfaces: morphological changes and mechanistic investigations“. In: Photochem. Photobiol. Sci. 5 (2006), 948-954
Series of experiments made under different experimental conditions brought evidence of two different reaction pathways: introduction of OH- and CO-groups at the polystyrene pathways is mainly due to the reaction of reactive oxygen species (hydroxyl radicals, atomic oxygen, ozone) produced in the gas phase between the VUV-radiation source and the substrate.
However, oxidative fragmentation leading to morphological changes, oxidation products of low molecular weight and eventually to mineralization of the organic substrate is initiated by electronic excitation of the polymer leading to C–C-bond homolysis and to a complex oxidation manifold after trapping of the C-centred radicals by molecular oxygen.
The pathways of oxidative functionalization or fragmentation could be differentiated by FTIR-ATR analysis of irradiated polystyrene surfaces before and after washing with acetonitrile and microscopic fluorescence analysis of the surfaces secondarily functionalized with the N,N,N-tridodecyl-triaza-triangulenium (TATA) cation.
Ozonization of the polystyrene leads to oxidative functionalization of the polymer surface but cannot initiate the fragmentation of the polymer backbone. Oxidative fragmentation is initiated by electronic excitation of the polymer (contact-mode AFM analysis), and evidence of the generation of intermediate C-centred radicals is given e.g. by experiments in the absence of oxygen leading to cross-linking (solubility effects, optical microscopy, friction-mode AFM) and disproportionation (fluorescence).