CИСТЕМА АНТИКРИЗИСНОГО УПРАВЛЕНИЯ КРЕДИТНЫМИ ОРГАНИЗАЦИЯМИ НА ОСНОВЕ СОВОКУПНОСТИ МАКРОЭКОНОМИЧЕСКИХ И МИКРОЭКОНОМИЧЕСКИХ ИНСТРУМЕНТОВ

The article covers the question of the complex crisis management system construction of the credit organization on the basis of the microeconomical and macroeconomical management tools range. It contains the data referring the place and role of the tools in the crisis management system and the complex model of the crisis management with the united statistical entity is built.В статье раскрывается вопрос построения комплексной системы антикризисного управления кредитной организацией на основе совокупности макроэкономических и микроэкономических инструментов. Обоснованы место и роль инструментов в системе антикризисного управления, приведена классификация инструментов и построена комплексная модель антикризисного управления кредитными организациями с использованием единого статистического органа

CRISIS MANAGEMENT SYSTEM OF THE CREDIT ORGANIZATION ON THE BASIS OF THE MACROECONOMICAL AND MICROECONOMICAL TOOLS RANGE.

The article covers the question of the complex crisis management system construction of the credit organization on the basis of the microeconomical and macroeconomical management tools range. It contains the data referring the place and role of the tools in the crisis management system and the complex model of the crisis management with the united statistical entity is built

Flow-induced effects in mixed surfactant mesophases

The adsorption of the cationic surfactant, hexadecyl trimethyl ammonium bromide, C16TAB, onto model cellulose surfaces, prepared by Langmuir-Blodgett deposition as thin films, has been investigated by neutron reflectivity. Comparison between the adsorption of C16TAB onto hydrophilic silica, a hydrophobic cellulose surface, and a regenerated (hydrophilic) cellulose surface is made. Adsorption onto the hydrophilic silica and onto the hydrophilic cellulose surfaces is similar, and is in the form of surface aggregates. In contrast, the adsorption onto the hydrophobic cellulose surface is lower and in the form of a monolayer. The impact of the surfactant adsorption and the in situ surface regeneration on the structure of the cellulose thin films and the nature of solvent penetration into the cellulose films are also investigated. For the hydrophobic cellulose surface, intermixing between the cellulose and surfactant occurs, whereas there is little penetration of surfactant into the hydrophilic cellulose surface. Measurements show that solvent exchange between the partially hydrated cellulose film and the solution is slow on the time scale of the measurements

Adsorption of Nonionic and Mixed Nonionic/Cationic Surfactants onto Hydrophilic and Hydrophobic Cellulose Thin Films

The adsorption of the nonionic surfactant hexaethylene monododecyl ether, C(12)E(6), and the mixed nonionic/cationic surfactants C(12)E(6) and hexadecyl trimethyl ammonium bromide, C(16)TAB, onto the hydrophilic and hydrophobic surfaces of thin cellulose films, formed by Langmuir-Blodgett, L-B, deposition, have been studied by neutron reflectivity. For the surfactant mixtures, considerable nonideal mixing is observed at both hydrophobic and hydrophilic surfaces. The results demonstrate that the C(12)E(6), C(12)E(6)/C(16)TAB mixture and solvent have a greater penetration into the cellulose film upon adsorption, compared to that observed in previous studies of C(16)TAB adsorbed onto cellulose, due to the presence of the nonionic surfactant. From the range of measurements made, it is concluded that both the presence of the nonionic surfactant and the nature of the cellulose films are both contributing factors to this increased penetration and swelling of the cellulose film