In this combined experimental and simulation investigation, a stream of HFE-7100 droplets striking a prewetted surface under constant heat flux was studied. An implicit free surface capturing technique based on the Volume-of-Fluid (VOF) approach was employed to simulate this process numerically. Experimentally, an infrared thermography technique was used to measure the temperature distribution of the surface consisting of a 100 nm ITO layer on a ZnSe substrate. The heat flux was varied to investigate the heat transfer behavior of periodic droplet impingement at the solid–liquid interface. In both experiments and simulations, the morphology of the impact zone was characterized by a quasi-stationary liquid impact crater. Comparison of the radial temperature profiles on the impinging surface between the experiments and numerical simulations yielded reasonable agreement. Due to the strong radial flow emanating from successive droplet impacts, the temperature distribution inside the crater region was found to be significantly reduced from its saturated value. In effect, the heat transfer mode in this region was governed by single phase convective and conductive heat transfer, and was mostly affected by the HFE-7100 mass flow rates or the number of droplets. At higher heat fluxes, the minimum temperature, and its gradient with respect to the radial coordinate, increased considerably. Numerical comparison between average and instantaneous temperature profiles within the droplet impact region showed the effect of thermal mixing produced by the liquid crowns formed during successive droplet impact events.
The Knoevenagel condensation between aldehydes and substrates with active methylene groups was applied to synthesise a series of 3-(4-substituted phenyl)-2-arylacrylonitriles (aryl = phenyl or pyridyl). Chloro-, fluoro-, or dimethylamino-substituted aryls and a cyano group attached to the double bond of acrylonitrile were studied. Previous studies showed that the condensation products were E isomers. The compounds synthesised were: 3-(4-chlorophenyl)-2-phenylacrylonitrile, 3-(4-chlorophenyl)-2-(pyridin-2-yl)acrylonitrile, 3-(4-chlorophenyl)-2-(pyridin-3-yl)acrylonitrile, 3-(4-chlorophenyl)-2-(pyridin-4-yl)acrylonitrile, 3-(4-fluorophenyl)-2-phenylacrylonitrile, 3-(4-fluorophenyl)-2-(pyridin-2-yl)acrylonitrile, 3-(4-fluorophenyl)-2-(pyridin-3-yl)acrylonitrile, 3-(4-fluorophenyl)-2-(pyridin-4-yl)acrylonitrile, 3-(4-dimethylaminophenyl)-2-phenylacrylonitrile, 3-(4-dimethylaminophenyl)-2-(pyridin-2-yl)acrylonitrile, 3-(4-dimethylaminophenyl)-2-(pyridin-3-yl)acrylonitrile, and 3-(4-dimethylaminophenyl)-2-(pyridin-4-yl)acrylonitrile. Structures were confirmed by IR, MS, and NMR spectral data. Molar absorption coefficient, absorbance, and fluorescence emission spectra were compared in order to evaluate the effects of substituents on phenyl and the position of nitrogen in pyridine moiety on the electronic properties of acrylonitrile derivatives prepared.
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