Filtern
Dokumenttyp
- Zeitschriftenartikel (5) (entfernen)
Sprache
- Englisch (5)
Schlagworte
- Polyimide (5) (entfernen)
Some applications of polymer films require the microstructuring of partly uneven substrates. This cannot be achieved by conventional photolithography, usually performed with ultraviolet short-pulse lasers (excimer, fourth harmonic Nd:YAG). When processing thermally sensitive or undoped polymers with low optical absorption, the use of femtosecond laser pulses can improve the ablation precision, also reducing the heat-affected zone. Therefore, a Ti:sapphire laser system was employed to perform ablation experiments on polyimide (PI). The irradiated areas were evaluated by means of optical and scanning electron microscopy. Highly oriented ripple structures, which are related to the polarization state of the laser pulses, were observed in the cavities. The relationship between the ablation threshold fluence and the number of laser pulses applied to the same spot is described in accordance with an incubation model.
A novel route toward halogen-free fire retardancy of polymers through innovative surface coating is described. Nanofiber mats based on polyimide are deposited on PA66 through electrospinning. Scanning electron microscopy is used to characterize the nanofibers. Cone calorimeter tests were performed to evaluate the fire performance. Because of their low thermal conductivity, electrospun nanofiber mats act not only as sacrificial layers but also as a protective surface that delays ignition. The effect is influenced by the fiber diameters and the imidization.
Detailed atomistic simulations were carried out for swelling polymer/gas systems related to experimental sorption and dilation data for CO2 and CH4 in three glassy polymers (polysulfone PSU, the polyimide 6FDA-TrMPD, and a polymer of intrinsic microporosity PIM-1) at 308 K (35 °C) and pressures up to 50 bar. Corresponding experiments were performed with a gravimetric sorption balance and a dilatometer based on a capacitance distance sensor. For each polymer/gas system molecular packing models were prepared and equilibrated for two reference states: the pure polymer is taken as reference for the respective 'unswollen' state and similarly the state of the highest penetrant pressure reached in the corresponding experiment is taken to represent the 'swollen' state. Models for the latter were constructed in agreement with experimental data (pressure, temperature, gas concentration and volume dilation). Concentration–pressure isotherms of each polymer/gas system were obtained using Grand Canonical Monte Carlo (GCMC) simulations for both reference states (depleted of gas molecules), which are in good agreement with the experimental data in the respective pressure range. As expected these isotherms – due to the simulation technique used, merely based on hole-filling in a static host matrix – do not represent the sorption behavior over a broader range of gas pressures which may involve significant structural rearrangements as well as swelling and relaxational phenomena. Nevertheless, a linear combination of the two GCMC-isotherms allows the interpolation in order to describe the nonlinear gas sorption in the glassy polymers under investigation covering the penetrant pressure range between the reference states in good agreement with the experimental results.
High performance polymer composites have been intensively investigated for tribological applications in air, but rarely in hydrogen environment. Author's previous benchmark of composites in liquid hydrogen (LH2) showed that graphite filled polymers have beneficial friction behaviour in this extreme condition. Therefore, further investigations have been undertaken in hydrogen environment. This paper presents first results obtained with polyimide composites filled with different types (natural, synthetic) and amounts of graphite in air, vacuum and hydrogen environments. A particular attention is taken to the influence of hydrogen on graphite as well as on the polymer matrix.
The influence of hydrogen environment on the friction and wear behavior of polyimide (PI) composites was investigated for two different PI-types (PI1 and PI2) filled with natural or synthetic graphite. Sliding tests were run against AISI 52100 steel and the worn surfaces as well as the transfer film were analyzed by means of SEM, EDX and Infrared Spectroscopy. Results indicate that the chemical structure of the polyimide has a major influence on the tribological behavior. While the friction of PI2 remains rather stable in all environments, PI1 showed very low friction in hydrogen without any lubricant. The lubricity of graphite was found to be more effective in hydrogen than in moist air.