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Abstract:The nonlocal polymerization-driven diffusion model (NPDD) has been shown to predict high spatial frequency cut-off in photopolymers and to accurately predict higher order grating components. We propose an extension to the NPDD model to account for the temporal response associated with polymer chain growth. An exponential response function is proposed to describe transient effects during the polymerization process. The extended model is then solved using a finite element technique and the nature of grating evolution examined in the case when illumination is stopped prior to the saturation of the grating recording process. Based on independently determined refractive index measurements we determine the temporal evolution of the refractive index modulation and the resulting diffraction efficiency using rigorous coupled wave theory. Material parameters are then extracted based on fits to experimental data for nonlinear and both ideal and non-ideal kinetic models.

Diffusion-based models of grating formation in photopolymers have been proposed in which the rate of monomer polymerization (removal) is directly proportional to the illuminating intensity inside the medium. However, based on photochemical considerations, the rate of polymerization is proportional in the steady state to the square root of the interference intensity. Recently it was shown that, by introducing a nonlocal response function into the one-dimensional diffusion equation that governs holographic grating formation in photopolymers, one can deduce both high-frequency and low-frequency cutoffs in the spatial-frequency response of photopolymer materials. Here the first-order nonlocal coupled diffusion equations are derived for the case of a general relationship between the rate of polymerization and the exposing intensity. Assuming a twoharmonic monomer expansion, the resultant analytic solutions are then used to fit experimental growth curves for gratings fabricated with different spatial frequencies. Various material parameters, including monomer diffusion constant D and nonlocal variance , are estimated.

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Plasma treatments are widely used to activate polymer surfaces prior to adhesive bonding. This study investigates the influence of plasma treatment conditions on the surface activation of a range of polymers using the PlasmaTreat (Open Air) system. In this study the effect of dc pulse plasma cycle time, compressed air flow rate and the plasma jet nozzle to substrate distance on the plasma discharge was examined. The influence that the dc pulse plasma cycle time parameter has on the activation of polypropylene, polystyrene and polycarbonate was also investigated. The level of polymer surface activation was evaluated based on the change in water contact angle after plasma treatment. The polymer surface properties were also monitored using AFM and XPS measurements. The heating effect of the plasma was monitored using both infrared thermographic camera and thermocouple measurements. Plasma diagnostics measurements were obtained using the photo‐diode and optical emission spectroscopy techniques. From this study it was concluded that for the PlasmaTreat system the level of plasma activation was closely correlated with the dc pulsed plasma cycle time, which is a measure of the plasma intensity. For example, the more intense plasma obtained with shorter cycle times gave higher levels of polymer activation. The optimized pulsed plasma cycle times were found to be specific for a given polymer type and related to their thermal properties. The pulsed cycle times were also found to correlate with both the substrate and plasma gas temperatures. magnified image