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Thermodynamic, non-equilibrium

In the other type of self-organization (dynamic self-organization), spontaneous ordering of the systems occurs under thermodynamically non-equilibrium conditions, in which various ordered structures with wavelengths tens to hundreds of thousands times larger than the size of the system components are formed by spatiotemporal synchronization of various factors [10-12]. The spatiotemporal order... [Pg.239]

The development of mixture sorption kinetics becomes increasingly Important since a number of purification and separation processes involves sorption at the condition of thermodynamic non-equilibrium. For their optimization, the kinetics of multicomponent sorption are to be modelled and the rate parameters have to be identified. Especially, in microporous sorbents, due to the high density of the sorption phase and, therefore, the mutual Influences of sorbing species, a knowledge of the matrix of diffusion coefficients is needed [6]. The complexity of the phenomena demands combined experimental and theoretical research. Actual directions of the development in this field are as follows ... [Pg.207]

Black foam films appear in thermodynamically non-equilibrium films in the form of black spots (see Section 3.2.2.2). These clearly expressed thin regions (but not holes as named in [e.g. 35,381]) expand, fuse and occupy the whole film area. Thus, CBF and NBF reach an equilibrium state. This process can be most distinctly observed in microscopic foam films (see Fig. 3.14). [Pg.230]

In contrast, inhibited plastics represent thermodynamically non-equilibrium systems that experience relaxation changes in their composition and structure, and are continuously exchanging substances with the ambient medium during their lifetime. [Pg.46]

This non-equilibrium chemical and physical (mechanical) state of inhibited plastics is caused by incorporated Cl and their carriers (PI) in concentrations exceeding the thermodynamic compatibility threshold with the polymer. The thermodynamic non-equilibrium is a useful property of inhibited plastics since it expands their anticorrosion functional features. The greater the deviation from the non-equilibrium state of such systems, the quicker the relaxation processes in them accompanied by the release of excess Cl into the ambient medium and to the object being protected. The structure and properties of the components of inhibited plastics Cl depend on their composition and can be carried to the mated part by either diffusion in the gaseous (thanks to Cl volatility) or liquid phase via its exudation, its mixture with a PI, or washing of water-soluble Cl and diffusion through the material moisture. These processes bring about mechanical relaxation of the polymer matrix. The point at which the inhibited anticorrosion material moves into a state of thermodynamic equilibrium is usually correlated with its protective ability. [Pg.46]

Thermodynamic compatibility of polymer CM components is observed rather infrequently as there is not commonly necessary to reach it. Polymer materials can be produced with preset properties even in conditions of limited compatibility between components. It is desirable to attain a thermodynamic non-equilibrium state for these materials for specific purposes, e.g. corrosionproofing by inhibited plastics. Process compatibility of components, on the other hand, should be treated as a requisite quality of CM. [Pg.47]

Experience has shown that these films must have a high glass transition temperature, Qrpically > 180 C, to insure thermal stability for many years. An important focus of current research is therefore directed to the enhancement of the thermal and temporal stability of x X The stability of polar order in the thermodynamically non-equilibrium glassy state varies from polymer to polymer. Chemical attachment of the chromophore to the polymer as a sidechain (2), as part of the mainchain (J), orinacrosslinkedstructure(4), has been found to retard the relaxaticm of alignment... [Pg.134]

In analysing thermohydraulic processes in the ALS, especially over long time intervals, it is important to use best estimate codes. This allows adequate modelling of the strong interrelations between the key thermohydraulic parameters and various local effects (such as thermodynamic non-equilibrium conditions). [Pg.50]

Plasma treatments The LJIP apparatus, operating at a frequency of 2.45 GHz, generated cold, thermodynamically non-equilibrium plasmas (1, 2), which may be conveniently classified as to type of procedure and vapor involved ... [Pg.456]

However, the phenomena of super-saturation of brines containing magnesium sulfate, borate is often found both in natural salt lakes and solar ponds around the world. Especially for salt lake brine and seawater systems, the natural evaporation is in a autogenetic process with the exchange of energy and substances in the open-ended system, and it is controlled by the radiant supply of solar energy with temperature difference, relative humidity, and air current, etc. In other word, it is impossible to reach the thermodynamic stable equilibrium, and it is in the status of thermodynamic non-equilibrium. [Pg.401]

For the thermodynamic non-equilibrium phase diagram of the sea water system as called "solar phase diagram" in the first, N.S. Kurnakov (1938) was in the first to report the experimental diagrams based on the natural brine evaporation, and further called... [Pg.401]

We can determine qualitatively the general conditions of self-organization by the formation of IPN occurring under thermodynamic non-equilibrium conditions. [Pg.295]

The main factor that defines interconnection of local order and the fractal nature of the structure of solid polymers is the fact that both these features are a reflection of the key property of these polymers- their thermodynamical non-equilibrium nature. The scales of fractal behaviour and indicated above correspond very well to cluster structure border sizes - to statistical segment length - to distance... [Pg.68]

Special attention is always paid to the questions of estimation of molecular mobility of polymer chains [54-56]. The reasons are obvious thermodynamically non-equilibrium solid-like media, particularly relaxation media, and their physical properties are defined by passing relaxation molecular processes in them, which in turn depend on features of the chemical constitution of the molecular chains and the structural organisation of the polymers [56]. As for parameters, there exist different points of view in describing these processes. So, for example, it is assumed that fast relaxations are defined by the mobility of free chains placed between densely packed domains, which are at the same time nodes of macromolecules physical entanglements network. Such treatment corresponds to the main postulates of the cluster model of the structure of polymers in the amorphous state [13], with the aid of which structure elements can be quantitatively described. [Pg.74]

The important distinction of Equations 2.15 and 2.16 is the fact that depends on one parameter in the first equation, which is typical for equilibrium Euclidean objects, and in the second on two parameters, which is typical for thermodynamically non-equilibrium fractal objects, therefore Equation 2.15 using the latter is incorrect. [Pg.76]

Hence, the results stated above have shown that fluctuation free volume in epoxy polymers possesses fractal structure. Therefor a microvoid forming it should be simulated by D -dimensional sphere. The size of the microvoids is controlled by the volume which is necessary for accumulation of the thermal fluctuations enei y required for their formation. The absolute values of can serve as characteristic of polymer structure thermodynamic non-equilibrium and for quasi-equilibrium structures the value of coincides with the data obtained according to the William-Landel-Ferry equation. Microvoids of fluctuation free volume form fractal structure, which is a mirror of polymer structure [152-158]. [Pg.269]

The results stated above suppose that simbateness of the values of Oy and as a function of any parameter (temperature, crosslinking density and so on) can be an individual case only. Equation 6.13 demonstrates that the indicated simbateness realisation condition is the criterion = const, or, as follows from Equation 6.14, (p = const. In other words, invariance in polymer structure is the condition of the realisation of the change in the simbateness of Oy and . Let us be reminded that amorphous polymers are thermodynamically non-equilibrium solids, for the description of which two parameters of order, as a minimum, are required according to the principle of Prigogine-Defay. It is obvious that Equation 6.13 satisfies this principle, whereas the linear correlation Oy( ) does not [36]. [Pg.296]

The plasma exists when a significant number of atoms or molecules are electrically charged or ionized by applying an electromagnetic field across a gas. The energy of the applied electric field arises mainly from free electrons, and the plasma achieves a thermodynamic non-equilibrium condition based on the high electron temperature and low gas temperature. Excitation, ionization and dissociation of atoms and molecules of the reactants and of the carrier gases to various radical and ion-radical species are achieved as a result of a sequence of inelastic electron-neutral collisions. [Pg.14]

Another fluid-dynamic option in ATHLET consists of a four-equation model, with balance equations for liquid mass, vapour mass, mixture energy and mixture momentum. It is based on a lumped-parameter approach. The solution variables are the pressure, mass quality and enthalpy of the dominant phase within a control volume, and the mass flow rates at the junctions. The entire range of fluid conditions, from sub-cooled liquid to superheated vapour, including thermodynamic non-equilibrium is taken into account, assuming the non-dominant phase to be at saturation. The option has also a mixture level tracking capability. [Pg.30]


See other pages where Thermodynamic, non-equilibrium is mentioned: [Pg.28]    [Pg.291]    [Pg.391]    [Pg.230]    [Pg.44]    [Pg.314]    [Pg.84]    [Pg.169]    [Pg.124]    [Pg.109]    [Pg.372]    [Pg.63]    [Pg.67]    [Pg.220]    [Pg.227]    [Pg.228]    [Pg.235]    [Pg.249]    [Pg.266]    [Pg.325]    [Pg.331]    [Pg.457]    [Pg.3]    [Pg.162]   
See also in sourсe #XX -- [ Pg.300 ]




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