A comparison of numerical and analytical radiative-transfer solutions for plane albedo of natural waters

Several numerical and analytical solutions of the radiative transfer equation (RTE) were compared for plane albedo in a problem of solar light reflection by sea water. The study incorporated the simplest case—a semi-infinite one-dimensional plane—parallel absorbing and scattering homogeneous layer illuminated by a monodirectional light beam. Inelastic processes (such as Raman scattering and fluorescence), polarization and air-water surface refraction-reflection effects, were not considered. Algorithms were based on the invariant imbedding method and two different variants of the discrete ordinate method (DOM). Calculations were performed using parameters across all possible ranges (single-scattering albedo ω₀ and refracted solar zenith angle θ₁), but with a special emphasis on natural waters. All computations were made for two scattering phase functions, which included an almost isotropic Rayleigh phase function and strongly anisotropic double-peaked Fournier-Forand-Mobley phase function. Models were validated using quasi-single-scattering (QSSA) and exponential approximations, which represent the extreme cases of ω₀→0 and ω₀→1, respectively. All methods yielded relative differences within 1.8% for modeled natural waters. An analysis of plane albedo behavior resulted in the development of a new extended QSSA approximation, which when applied in conjunction with the extended Hapke approximation developed earlier, resulted in a maximum relative error of 2.7%. The study results demonstrated that for practical applications, the estimation of inherent optical properties from observed reflectance can best be achieved using an extended Hapke approximation.     

Synthesis of tetraarm stars with polyetherimide-polyether block copolymer arms

Russian Chemical Bulletin - The method of one-stage catalytic polycyclocondensation according to the B4 + AB scheme was used to synthesize new tetraarm star-shaped oligoimides (SOIs) with terminal...     

Corrosion of Gold Anode in an Aqueous Solution of N,N-Dimethylpropane-1,3-diamine

Russian Journal of Organic Chemistry - The kinetics and mechanism of corrosion of gold anode in a weakly basic aqueous solution of N,N-dimethylpropane-1,3-diamine have been studied by cyclic...     

exo- and endo-Complexes of Fe(0) with Carbon Allotropic Modifications on the Example of Fullerene С60: a Density Function Theory Study

Russian Journal of General Chemistry - Structures of exo- and endo-complexes of fullerene C60 with zero-valent Fe0, in which the metal is localized inside and outside fullerene molecule,...     

Reaction kinetics and solubility in water‐organic binary solutions are governed by similar solvation equilibria

The solvation effects observed in water‐organic solutions were studied by combining data for reaction kinetics and dissolution equilibria by means of a linear free‐energy (similarity) analysis. Kinetic data for the pH‐independent hydrolysis of (4‐methoxyphenyl)‐2,2‐dichloroacetate measured in this work and solubility data for naphthalene, and other substrates of low polarity, in aqueous binary mixtures of methanol, ethanol, acetonitrile, dimethyl sulfoxide (DMSO), and 1,4‐dioxane were used. Linear similarity relationships were discovered for these data over the full range of solvent compositions studied. To gain insight into the similarities observed between these different phenomena, molecular dynamics simulations were carried out for naphthalene and an ester in water–acetonitrile solutions. The results revealed considerable preferential solvation of these substrates by the co‐solvent. Linear relationships between the experimental data and the mole fractions of acetonitrile in the solvation shells of substrates were found. Surprisingly, a linear relationship was found between the mole fractions of acetonitrile in the solvation shells of the ester and naphthalene. This linearity indicated that a similar solvation mechanism governs even such different phenomena as dissolution and reaction kinetics. The relationships between the experimental data and the results of the molecular dynamics calculations found in this work explained the solvent effect observed in water‐organic solutions on the molecular level. Copyright © 2015 John Wiley & Sons, Ltd.     

Analysis of conditions for determining the thermophysical characteristics of energetic materials by the laser pulse method

An analysis of conditions for determining the thermophysical characteristics of energetic materials by the laser pulse method is performed. Based on the results of numerical solution of the heat conduction problems for a sample of a material irradiated with a short heating laser pulse corresponding to actual experimental conditions, the time dependences on the sample surface temperature are determined. The heat pulse duration required to determine the thermophysical properties of materials and the ignition delay time are compared. It is shown that the determination of the thermophysical characteristics of a typical energetic material by the laser pulse method is possible at pulse durations of no longer than 0.24 s.     

Self-consistent inhomogeneity of quantum wells in II–VI semiconductors

An X-ray diffraction method that uses a slightly diverging (3′) beam and maximally attainable diffraction angles ? _B (as large as 77°) was developed to study quantum wells (QWs) with widths of 5–8 nm separated by wide (100–220 nm) barrier layers. The advantage of this method compared to the use of a parallel beam is an increase by two orders of magnitude in the intensity of the beam incident on the sample and an increase in the probability of diffraction for all QWs as a unified single crystal. It is found that the growth on GaAs substrates misoriented by 10° from the (001) plane in the [111]_II direction brings about monoclinization of crystal lattices of the QW layers and barrier layers in opposite directions. Inhomogeneity of composition over the thickness of each well is observed. In the case of growth of a ZnSe/ZnMgSSe structure in which the layers have a crystal-lattice period close to the lattice period of the GaAs substrate, the QWs are inhomogeneously doped with elements from the composition of the barrier layers. The inhomogeneity of QW composition observed in the growth of mismatched layers in ZnCdSe/ZnSSe and ZnCdS/ZnSSe structures is caused by the fact that mismatch between the lattice parameters of QWs and barriers stimulates the growth of self-consistent compositions; this occurs due to a decrease in the Cd concentration in the Zn_1?x Cd _x Se QW in the initial stages of growth compared to the Cd concentration in the flow of gases and an increase in the Zn concentration in the Cd_1?x Zn _x S QW at small values of x up to the concentration matching GaAs (x = 0.4). The mismatch stresses are partially relaxed via dislocations with the (111)_II glide planes, as a result of which is observed the combination of rotation of the crystal planes of the layers and QW around the [1\(\overline 1 \)0] axis and almost cylindrical bending of the entire sample around the perpendicular [110] axis. Mismatch between lattice parameters of the ZnMgSSe barrier layers and the substrate brings about decomposition of these layers into two phases; this decomposition is caused by thermodynamic instability of the alloy.     

Fiber laser cleaning of metal mirror surfaces for optical diagnostic systems of the ITER

The results of experimental studies into efficiency of removal of films with a complex composition from metal mirrors by pulsed fiber laser irradiation are presented. It is shown that the initial reflectivity of optical elements can be restored by the selection of modes of irradiation impacting the surface with the sputtered film. Effective cleaning is performed by radiation with a power density lower than 10⁷ W/cm². The removal of contaminations at such a relatively low power density occurs in a solid phase, owing to which the thermal effect on the mirror is insignificant.