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Energetics States

The small and positive values of enthalpy of solution of water in AOT-reversed micelles indicate that its energetic state is only slightly changed and that water solubilization (unfavorable from an enthalpic point of view) is driven mainly by a favorable change in entropy (the destructuration of the water at the interface and its dispersion as nanodroplets could be prominent contributions) [87],... [Pg.482]

The kinetic factor is proportional to the energetic state of the system and (for heterogeneous catalytic systems) the number of active sites per unit volume (mass) of catalyst. The driving-force group includes the influence of concentration and distance from chemical equilibrium on the reaction rate, and the hindering group describes the hindering effect of components of the reaction mixture on the reaction rate. The kinetic factor is expressed as the rate constant, possibly multiplied by an equilibrium constant(s) as will be shown later. [Pg.277]

The energetic state of any system, including that of a cell and an organism, can be defined in terms of this very important equation. The free energy is expressed in kilojoules per mole of substance, kJ/ mol. [Pg.174]

The Yl/A isotherms of the racemic and enantiomeric forms of DPPC are identical within experimental error under every condition of temperature, humidity, and rate of compression that we have tested. For example, the temperature dependence of the compression/expansion curves for DPPC monolayers spread on pure water are identical for both the racemic mixture and the d- and L-isomers (Fig. 13). Furthermore, the equilibrium spreading pressures of this surfactant are independent of stereochemistry in the same broad temperature range, indicating that both enantiomeric and racemic films of DPPC are at the same energetic state when in equilibrium with their bulk crystals. [Pg.75]

It is also clear that for a complete description of a catalytic system, as investigated here, one needs the complete functional describing the microkinetics in dependence on the energetic states of the catalyst surface. [Pg.298]

Mitochondria are distinct organelles with two membranes. The outer membrane limits the organelle and the inner membrane is thrown into folds or shelves that project inward and are called cristae mitochondriales. The uptake of most mitochondrion-selective dyes is dependent on the mitochondrial membrane potential. Conventional fluorescent stains for mitochondria, such as rhodamine and tetramethylrosamine, are readily sequestered by functioning mitochondria. They are, however, subsequently washed out of the cells once the mitochondrion s membrane potential is lost. This characteristic limits their use in experiments in which cells must be treated with aldehyde-based fixatives or other agents that affect the energetic state of the mitochondria. To overcome this limitation, the research... [Pg.87]

Usually, in amorphous molecular materials, charge transport is described by a disorder formalism that assumes a Gaussian distribution of energetic states of the molecules between which the charges jump [246]. The mobility is then given by... [Pg.149]

Plasmas can be classified as either thermal or non-thermal. " Thermal plasma is a highly energetic state of matter, characterized by thermal equilibrium between the three components of the plasma electrons, ions, and neutrals. However, it requires high-energy input to achieve high temperatures. Researchers at MIT used a non-catalytic thermal plasma technology to produce H2 from liquid hydrocarbons. Non-catalytic processes are beyond the scope of this work, and will not be discussed. [Pg.245]

In all factors are collected which are independent of the momentary energetic state of the reactants, like collision numbers, geometrical and also normalizing factors [e.g. A from Eqs. (20, 22)] etc. The x(E) in the integrals represent the transition probability for electrons in case the condition of energy conservation is fulfilled (Emitiai =-Efinai)- The D(E) functions denote the densities of vacant or occupied electron states in the electrode. [Pg.42]

The Boltzmannian Distribution. The general theory of chemical reaction rates is associated with the reactivity of rarely occurring, highly energetic states. It seems improbable that electrochemical reactions in solution will differ radically from chemical reactions in solution so as not to involve stales above the ground state. [Pg.750]

AMP concentration is a much more sensitive indicator of a cell s energetic state than is ATP. Normally cells have a far higher concentration of ATP (5 to 10 mM) than of AMP (<0.1 mM). When some process (say, muscle contraction) consumes ATP, AMP is produced in two steps. First, hydrolysis of ATP produces ADP, then the reaction catalyzed by adenylate kinase produces AMP ... [Pg.571]

It is always convenient to use intensive thermodynamic variables for the formulation of changes in energetic state functions such as the Gibbs energy G. Since G is a first order homogeneous function in the extensive variables V, S, and rtk, it follows that [H. Schmalzried, A.D. Pelton (1973)]... [Pg.292]

If correlations do exist for simple metals, predictions are much more difficult for composite materials. On the other hand, cathode activation has two aims (i) to replace active but expensive materials with cheaper ones, and (ii) to enhance the activity of cheaper materials so as to approach or even surpass that of the more expensive catalysts. In the case of pure metals there is little hope to find a new material satisfying the above requirements since in the volcano curve each metal has a fixed position which cannot be changed. Therefore, activation of pure metals can only be achieved by modifying its structure so as to enhance the surface area (which has nothing to do with electrocatalysis in a strict sense), and possibly to influence the mechanism and the energetic state of the intermediate in the wanted direction. This includes the preparation of rough surfaces but also of dispersed catalysts. Examples will be discussed later. [Pg.7]


See other pages where Energetics States is mentioned: [Pg.1071]    [Pg.1071]    [Pg.372]    [Pg.381]    [Pg.109]    [Pg.208]    [Pg.116]    [Pg.124]    [Pg.107]    [Pg.276]    [Pg.180]    [Pg.48]    [Pg.31]    [Pg.145]    [Pg.256]    [Pg.298]    [Pg.48]    [Pg.226]    [Pg.198]    [Pg.361]    [Pg.196]    [Pg.24]    [Pg.26]    [Pg.264]    [Pg.127]    [Pg.23]    [Pg.2]    [Pg.401]    [Pg.797]    [Pg.22]    [Pg.1448]    [Pg.256]    [Pg.134]    [Pg.18]    [Pg.254]   
See also in sourсe #XX -- [ Pg.38 , Pg.40 , Pg.43 , Pg.44 , Pg.50 ]




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Energetic states diversity

Energetically distributed trapping states

Energetics and Reaction Pathways Metallic Edge States as Active Sites

Energetics of the transition state

Equi-energetic states

Ground-state wavefunctions energetics

Lattice Energies and Ionic Radii Connecting Crystal Field Effects with Solid-State Energetics

Solid-state energetics

Solid-state energetics charge density

Solid-state reactions energetic chains

Spin-state energetics, relative

State, energetic

State, energetic

The Chemisorbed State Energetic Aspects

Transition state, energetics

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