Barbeeboykin8540

Critical micelle concentration (CMC) is the main chemical-physical parameter to be determined for pure surfactants for their characterization in terms of surface activity and self-assembled aggregation. The CMC values can be calculated from different techniques (e.g., tensiometry, conductivity, fluorescence spectroscopy), able to follow the variation of a physical property with surfactant concentrations. Different mathematical approaches have been applied for the determination of CMC values from the raw experimental data. Most of them are independent of the operator, despite not all of the fitting procedures employed so far can be applied in all techniques. In this experimental work, the second derivative of the experimental data has been proposed as a unique approach to determine the CMC values from different techniques (tensiometry, conductimetry, densimetry, spectrofluorimetry, and high-resolution ultrasound spectroscopy). To this end, the CMC values of five different surfactants, specifically three anionic (sodium dodecyl sulfate, sodium deoxycolate, and N-lauroyl sarcosinate) and two nonionic, such as polyethylene glycol ester surfactants [polyethylenglicol (8) monostearate and polyethylenglicol (8) monolaurate], have been determined by this approach. The "second-derivate" approach provides a reliable determination of the CMC values among all of the techniques investigated, which were comparable to those calculated by the other operator-free routinely methods employed, such as segmental linear regression or Boltzmann regression. This study also highlighted the strengths and shortcomings of each technique over the others, providing an overview of the CMC values of commonly used anionic and nonionic surfactants in the pharmaceutical field, determined by employing different experimental approaches.Water confined by hydrophilic materials shows unique transport properties compared to bulk water, thereby offering new opportunities for the development of nanofluidic devices. Recent experimental and numerical studies showed that nanoconfined water undergoes liquid- to solid-phase-like transitions depending on the degree of confinement. In the case of water confined by graphene layers, the van der Waals forces are known to deform the graphene layers, whose bending leads to further nonuniform confinement effects. Despite the extensive studies of nanoconfined water under equilibrium conditions, the interplay between the confinement and rheological water properties, such as viscosity, slip length, and normal stress differences under shear flow conditions, is poorly understood. The current investigation uses a validated all-atom nonequilibrium molecular dynamics model to simultaneously analyze the continuum transport and atomistic structural properties of water in a slit between two moving graphene walls under Couette flow conditions. A range of different slit widths and velocity strain rates are considered. YD23 nmr It is shown that under subnanometer confinement, water loses the rotational symmetry of a Newtonian fluid. Under such conditions, water transforms into ice, where the atomistic structure is completely insensitive to the applied shear force and behaves like a frozen slab sliding between the graphene walls. This leads to the shear viscosity increase, although it is not as dramatic as the normal force increase that contributes to the increased friction force reported in previous experimental studies. On the other end of the spectrum, for flows at large velocity strain rates in moderate to large slits between the graphene walls, water is in the liquid state and reveals shear thinning behavior. In this case, water exhibits a constant slip length on the wall, which is typical of liquids in the vicinity of hydrophobic surfaces.Advancing and receding angles are physical quantities frequently measured to characterize the wetting properties of a rough surface. Thermodynamically, the advancing and receding angles are often interpreted as the maximum and minimum contact angles that can be formed by a droplet without losing its stability. Despite intensive research on wetting of rough surfaces, the gravitational effect on these angles has been overlooked because most studies have considered droplets smaller than the capillary length. In this study, however, by combining theoretical and numerical modeling, we show that the shape of a droplet smaller than the capillary length can be substantially modified by gravity under advancing and receding conditions. First, based on the Laplace pressure equation, we predict the shape of a two-dimensional Cassie-Baxter droplet on a textured surface with gravity at each pinning point. Then, the stability of the droplet is tested by examining the interference between the liquid surface and neighboring plity of rough surfaces.Herein, we disclose the synthesis of diaryl selenides through an unexpected C-Se coupling between aryl benzyl selenoxides and phenols. The synthetic significance of the method is that it provides a mild, rapid, and metal-free access to organoselenides in high yields with excellent functional group tolerance. This coupling of aryl benzyl selenoxides reveals a completely new reaction possibility compared with aryl sulfoxides. We also probed the reaction mechanism of this unexpected transformation through experimental studies and revealed a special Se(IV)-Se(III)-Se(II) reaction pathway.Nitroaromatic explosives in wastewater are hardly degraded, which seriously endangers the ecological environment and human safety. We report a core-shell structure hybrid material (IR-MOF3@COF-LZU1) with high crystallinity and graded porosity. It is an effective visible-light-driven photocatalyst that degrades p-nitrophenol (PNP). After 3.5 h, PNP was degraded well under visible light, and it is proven that the photocatalytic degradation is efficient. In addition, this photocatalytic activity adhered to pseudo-first-order kinetics, and a possible photocatalytic mechanism was discussed in detail.The conical intersection dynamics of thiophenol is studied by computing the stimulated X-ray resonant Raman spectroscopy signals. The hybrid probing field is constructed of a hard X-ray narrowband femtosecond pulse combined with an attosecond broadband X-ray pulse to provide optimal spectral and temporal resolutions for electronic coherences in the level crossing region. The signal carries phase information about the valence-core electronic coupling in the vicinity of conical intersections. Two conical intersections occurring during the course of the S-H dissociation dynamics can be distinguished by their valence-core transition frequencies computed at the complete active space self-consistent field level. The X-ray pulse is tuned such that the Raman transition at the first conical intersection between 1πσ* and 11ππ* involves higher core levels, while the Raman transition at the second conical intersection between 1πσ* and S0 involves the lowest core level in the sulfur K-edge.