296 research outputs found
Институциональные условия усиления внедрения инвестиций интенсивного типа
Большое значение в процессе повышения эффективности общественного воспроизводства на основе усиления внедрения инноваций и инвестиций интенсивного типа имеет создание оптимальных институциональных условий и предпосылок. В этой связи в работе исследуются факторы формирования оптимальной институциональной среды как основы интенсификации российской экономики.Велике значення у процесі підвищення ефективності суспільного відтворення на основі посилення впровадження інновацій та інвестицій інтенсивного типу має створення оптимальних інституційних умов і передумов. У зв'язку із цим у роботі досліджуються чинники формування оптимального інституційного середовища як основи інтенсифікації російської економіки.Creation of optimal institutional conditions and preconditions is of great importance in the process of increasing the efficiency of public reproduction on the basis of strengthening the introduction of innovations and investments of intensive type. In this respect the factors of formation of optimal institutional environment as the bases for intensification of the Russian economy are analyzed
The interlayer cohesive energy of graphite from thermal desorption of polyaromatic hydrocarbons
We have studied the interaction of polyaromatic hydrocarbons (PAHs) with the
basal plane of graphite using thermal desorption spectroscopy. Desorption
kinetics of benzene, naphthalene, coronene and ovalene at sub-monolayer
coverages yield activation energies of 0.50 eV, 0.85 eV, 1.40 eV and 2.1 eV,
respectively. Benzene and naphthalene follow simple first order desorption
kinetics while coronene and ovalene exhibit fractional order kinetics owing to
the stability of 2-D adsorbate islands up to the desorption temperature.
Pre-exponential frequency factors are found to be in the range
- as obtained from both Falconer--Madix (isothermal
desorption) analysis and Antoine's fit to vapour pressure data. The resulting
binding energy per carbon atom of the PAH is 5 meV and can be identified
with the interlayer cohesive energy of graphite. The resulting cleavage energy
of graphite is ~meV/atom which is considerably larger than previously
reported experimental values.Comment: 8 pages, 4 figures, 2 table
Multiple Scale Reorganization of Electrostatic Complexes of PolyStyrene Sulfonate and Lysozyme
We report on a SANS investigation into the potential for these structural
reorganization of complexes composed of lysozyme and small PSS chains of
opposite charge if the physicochemical conditions of the solutions are changed
after their formation. Mixtures of solutions of lysozyme and PSS with high
matter content and with an introduced charge ratio [-]/[+]intro close to the
electrostatic stoichiometry, lead to suspensions that are macroscopically
stable. They are composed at local scale of dense globular primary complexes of
radius ~ 100 {\AA}; at a higher scale they are organized fractally with a
dimension 2.1. We first show that the dilution of the solution of complexes,
all other physicochemical parameters remaining constant, induces a macroscopic
destabilization of the solutions but does not modify the structure of the
complexes at submicronic scales. This suggests that the colloidal stability of
the complexes can be explained by the interlocking of the fractal aggregates in
a network at high concentration: dilution does not break the local aggregate
structure but it does destroy the network. We show, secondly, that the addition
of salt does not change the almost frozen inner structure of the cores of the
primary complexes, although it does encourage growth of the complexes; these
coalesce into larger complexes as salt has partially screened the electrostatic
repulsions between two primary complexes. These larger primary complexes remain
aggregated with a fractal dimension of 2.1. Thirdly, we show that the addition
of PSS chains up to [-]/[+]intro ~ 20, after the formation of the primary
complex with a [-]/[+]intro close to 1, only slightly changes the inner
structure of the primary complexes. Moreover, in contrast to the synthesis
achieved in the one-step mixing procedure where the proteins are unfolded for a
range of [-]/[+]intro, the native conformation of the proteins is preserved
inside the frozen core
A General Approach for Predicting the Filtration of Soft and Permeable Colloids: The Milk Example
Membrane filtration operations (ultra-, microfiltration) are now extensively used for concentrating or separating an ever-growing variety of colloidal dispersions. However, the phenomena that determine the efficiency of these operations are not yet fully understood. This is especially the case when dealing with colloids that are soft, deformable, and permeable. In this paper, we propose a methodology for building a model that is able to predict the performance (flux, concentration profiles) of the filtration of such objects in relation with the operating conditions. This is done by focusing on the case of milk filtration, all experiments being performed with dispersions of milk casein micelles, which are sort of ″natural″ colloidal microgels. Using this example, we develop the general idea that a filtration model can always be built for a given colloidal dispersion as long as this dispersion has been characterized in terms of osmotic pressure Π and hydraulic permeability k. For soft and permeable colloids, the major issue is that the permeability k cannot be assessed in a trivial way like in the case for hard-sphere colloids. To get around this difficulty, we follow two distinct approaches to actually measure k: a direct approach, involving osmotic stress experiments, and a reverse-calculation approach, that consists of estimating k through well-controlled filtration experiments. The resulting filtration model is then validated against experimental measurements obtained from combined milk filtration/SAXS experiments. We also give precise examples of how the model can be used, as well as a brief discussion on the possible universality of the approach presented here
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