RESUMEN
A new process is reported for the incorporation of a fluoropolymer into a solid perovskite film. Poly(trifluoroethyl methacrylate) [CH2C(CH3)(CO2CH2CF3)]n was delivered to methylammonium lead iodide (CH3NH3PbI3) perovskite films by crystallizing the film in supercritical carbon dioxide/ethanol containing the dissolved fluoropolymer. The surface was characterized before and after fluoropolymer exposure using scanning electron microscopy, Raman spectroscopy, and contact angle measurements. The results indicate that the fluoropolymer was incorporated into the perovskite film during the supercritical fluid crystallization process. The incorporation of a hydrophobic fluoropolymer into perovskite has the potential to improve resistance to environmental degradation.
RESUMEN
The fluorescence intensity and transport kinetics of uranyl into mesoporous silica gel was measured in the presence of six naturally occurring cations. It was shown that the presence of the cations can reduce the fluorescence intensity of the uranyl through collision quenching and through competition for the silica gel surface sites. Stern-Volmer quenching coefficients were obtained by measuring the uranyl fluorescence as a function of cation concentration. The cations compete with uranyl to occupy silica gel surface sites and cause a decrease in uranyl fluorescence intensity and a reduction in the uranyl saturation time constant. Energy-dispersive x-ray spectroscopy (EDS) was used to measure the weight percentage of uranium and the cations in the silica gel samples and these results correlated well with the results of the saturation time constant measurements. The results of this study show that, at high concentrations, the presence of cations in water can influence the fluorescence intensity and transport kinetics of uranyl into mesoporous silica gel.
RESUMEN
Light scattering was used to measure the time-dependent loss of air entrapped within a submerged microporous hydrophobic surface subjected to different environmental conditions. The loss of trapped air resulted in a measurable decrease in surface reflectivity and the kinetics of the process was determined in real time and compared to surface properties, such as porosity and morphology. The light-scattering results were compared with measurements of skin-friction drag, static contact angle, and contact-angle hysteresis. The in situ, noninvasive optical technique was shown to correlate well with the more conventional methods for quantifying surface hydrophobicity, such as flow slip and contact angle.
RESUMEN
We show that nanoporous anodic alumina films, with pore diameters in the range 10-80 nm, can be transformed from being very hydrophilic (or super-hydrophilic) to very hydrophobic (or super-hydrophobic) by coating the surface with a thin (2-3 nm) layer of a hydrophobic polymer. This dramatic transformation happens as a result of the interplay between surface morphology and surface chemistry. The coated surfaces exhibit 'sticky' hydrophobicity as a result of ingress of water into the pores by capillary action. The wetting parameters (contact angle and contact angle hysteresis) exhibit qualitatively different dependences on pore diameters in coated and uncoated films, which are explained by invoking appropriate models for wetting.
RESUMEN
An in situ mesopourous surface imprinted polymeric (SIP) sensor was synthesized for a highly sensitive, selective, and kinetically faster detection of the high-vapor-pressure nerve gas surrogate methyl salicylate (MES). Visual detection occurred on the filtrate thin films at 25 pM. Other nerve gas surrogates, TP, DMP, DMMP, PMP, and 1,4-thioxane, were tested and showed a decrease in sensitivity compared to MES. In addition, 2,6-dipicolinic acid (DPA), a biological indicator, was also investigated and showed a decrease in sensitivity compared to MES. Finally, the detection plateau was reached at 40 s and at 1.5 x 10(-4) M from pH 6-11.
