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On the Application of the Auxiliary Problem Principle

The auxiliary problem principle (APP) derives from a general theory on decomposition-coordination methods establishing a comprehensive framework for both one-level and two-level methods. In this paper, the results of the two-level methods of APP are specialized for an efficient application to some engineering problems.     

Diffusion Structural Analysis Study of Titania Films Deposited by Sol-Gel Technique on Silica Glass

The diffusion structural analysis (DSA) was used to characterize microstructure changes of hydrous titania gel films under in situ conditions of heating. TG and DTA were used in order to elucidate the processes controlling the formation of anatase film during heating of hydrous titania gel film. The annealing of porosity and near surface structure defects of the dehydrated titania films was indicated by DSA in the temperature range 255–700°C as the decrease of radon release rate. It was demonstrated that the annealing was enhanced on heating in oxygen in comparison with heating in argon. The DSA experimental results were compared with model curves describing the radon diffusion mobility and the annealing of radon diffusion paths.     

Mechanisms for the SAR Imaging of the Ocean

We perform a comparative analysis of two mechanisms for the formation of a synthetic aperture radar (SAR) image of the ocean, which are related to orbital velocities on the surface. It is shown that the mechanism of fluctuations of the effective density of scatterers, which is commonly accepted at present as the physical basis for the SAR diagnostics of roughness, actually works only in the case of a sufficiently flat swell. In the presence of wind roughness, the dominant role is played by another mechanism, namely, fluctuations of the number of surface elements whose images are randomly shifted and superimposed in the image plane due to orbital velocities. In the case of a developed wind roughness propagated in the azimuthal direction, the power contributions of two above-mentioned mechanisms to the SAR imaging of the ocean differ by about two orders of magnitude.     

Angular correlations in the decays of two unstable identical particles with close momenta

For the decay of two identical particles with close momenta, the angular correlations between the directions of emission of decay products are considered on the basis of the model of independent single-particle sources emitting unstable unpolarized particles of nonzero spin. These correlations reflect spin correlations that are caused by quantum-statistics and final-state-interaction effects. A general theory of angular correlations in the decays of two arbitrarily polarized particles (resonances) is constructed.     

Spectroscopic Study of Proton-Transfer Interaction between Methylbis(1-silatranylmethyl)amine and Phenols

Acid-base interaction of phenol and 4-nitrophenol with methylbis(1-silatranylmethyl)amine in acetonitrile is completely shifted toward formation of solvation-separated ion pairs. The unusually high electron-donor power of the exocyclic nitrogen atom in the amine is due to the presence of two silatranylmethyl groups exhibiting a super-electron-donor inductive effect.     

Complexes of Some Pyrido[1,2-a]pyrimidinium Perchlorates with Scandium,Yttrium, and Lanthanum. Crystal and Molecular Structure of 3-Chloro-9-Hydroxy-2,4-Dimethylpyrido[1,2-a]pyrimidinium Perchlorate

Complexes of scandium, yttrium, and lanthanum nitrates with 3-chloro-9-hydroxy-2,4-dimethylpyrido[1,2-a]pyrimidinium perchlorate (HL¹ClO₄) and 9-hydroxy-2,4-dimethylpyrido[1,2-a]pyrimidinium perchlorate (HL²ClO₄) were obtained. Their composition was formulated as Sc(LClO₄)₂(NO₃) and M(LClO₄)₂(NO₃)₂ (L = L¹ or L²; M = Y or La); structures for the complexes obtained were proposed. The crystal and molecular structure of HL¹ClO₄ was determined. Dissociation and complexation of HL¹ClO₄ and HL²ClO₄ in aqueous ethanol were studied using the spectroscopic method. Ligand dissociation and complexation constants were calculated. It was shown that a chlorine-containing organic ligand only slightly changes the composition and stability of the metal complexes.