Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Energy excessive

The validity of mean field theory for N —y oo has striking consequences for the initial stages of phase separation. " In a metastable state slightly inside the coexistence curve, the nucleation free energy barrier is due to spherical droplets with a radius R The free energy excess of a droplet is written in terms of bulk and surface terms " "... [Pg.200]

For excitation of solutes with 0-0 transitions v0o>v (antiStokes spectral region of absorption), the situation is the opposite at the initial instant of time, the spectra are red-shifted as compared to the steady state spectra, Av1 (l)<0. In this case, the return of the spectrum to its normal position during configurational relaxation will lead to a blue shift with time. From the physical point of view, this means that the intermolecular energy excess, which the solvates possess before excitation, is partially converted into emitted energy leading to an increase in the radiation frequency with time. That is why the process may be called the up-relaxation of the fluorescence spectra. [Pg.206]

The energy excess possessed by a broken, as compared with an unbroken, crystal exists because the atoms (or ions, or molecules) at the rupture surface are attracted by the solid stronger than by the vacuum. This field of force causes re-arrangement of the particles but produces no surface tension. [Pg.62]

In many cases the CALPHAD method is applied to systems where there is solubility between the various components which make up the system, whether it is in the solid, liquid or gaseous state. Such a system is called a solution, and the separate elements (i.e., Al, Fe...) and/or molecules (i.e., NaCl, CuS...) which make up the solution are defined as the components. The model description of solutions (or solution phases) is absolutely fundamental to the CALPHAD process and is dealt with in more detail in chapter S. The present chapter will discuss concepts such as ideal mixing energies, excess Gibbs energies, activities, etc. [Pg.61]

Synthesis of fatty acids and their incorporation into triacylglycerols are stimulated during this time of energy excess. [Pg.58]

The energy increment that is passed on has been called the enthalpy excess, but might better be called the thermal or internal energy excess, for the products at the iso-choric adiabatic explosion temperature have, by definition, exactly the same total internal energy as the original undetonated explosive... [Pg.267]

Jan 1968. The above write-up is based principally on Dunkle s Energy Excess in Detonation and in Flames , given in his "High-Lights of Session 14 , The 7thSympCombstn, dated 12 Nov, 1958)... [Pg.268]

Excess Free Energy, Excess Enthalpy, and Excess Entropy... [Pg.57]

Reaction 9.133 represents an alternate fate for C, in which collision with a third body M carries away (as translational energy) excess internal energy of C, leaving behind a stable C molecule. This so-called stabilization reaction, with rate constant ks, provides an alternate product-formation channel. The reactive intermediate C can also react via 9.134, the main channel to form products D and E. This reaction channel proceeds with rate constant kr. [Pg.394]

Synthesis and degradation of triacylglycerols in adipose tissue. Fatty acids are delivered to adipose tissue. In times of energy excess these are converted to triacylglycerols and stored until needed, at which point the triacylglycerols are converted back to fatty acids. [Pg.567]

Energies, Excess Enthalpies, Excess Volumes, and Isothermal Compressibilities of Cyclohexane + 2,3-Dimethylbutane , J. Client. Thermodyn., 6, 35-41 (1974). J. B. Ott, K. N. Marsh, and R. H. Stokes, Excess Enthalpies, Excess Gibbs Free Energies, and Excess Volumes for (Cyclohexane + n-Hexane), and Excess Gibbs Free Energies and Excess Volumes for (Cyclohexane + Methylcyclohexane) at 298.15 and 308.15 K , J. Chem. Thermodyn., 12, 1139-1148 (1980). [Pg.306]

Let us now determine what the material particle, possessing the chemical energy excess, provides for the communication channel (conjugation) between respiration and phosphorylation. According to data obtained by biochemists, there are three highly active intermediate products... [Pg.66]

The rates of the forward and backward transfers with the free-energy excess AG relate to each other according to the detailed balance principle ... [Pg.152]

A spectacular result can be seen in the action spectrum (Figure 4-6) the vibrational bands become narrower when the energy excess in the system increases, which indicates that the reaction time is longer as the energy in the intermediate state is larger. As discussed earlier, this surprising behavior has been interpreted in terms of rotational excitation of the HCl molecule within the complex. This... [Pg.114]

Excited-state relaxation can proceed spontaneously in monomolecular processes or can be stimulated by a molecular entity (quencher) that deactivates (quenches) an excited state of another molecular entity, by energy transfer, electron transfer, or a chemical mechanism [lj.The quenching is mostly a bimolecular radiationless process (the exception is a quencher built into the reactant molecule), which either regenerates the reactant molecule dissipating an energy excess or generates a photochemical reaction product (Figure 4.1). [Pg.26]

The factors that contribute to the reactivity of an excited state include not only the energy excess, but also the intrinsic reactivity of the specific electronic arrangement and the relative efficiencies of the different competing pathways. The factors are all correlated and therefore the reaction pathways allowed by the correlation rules are often different from those of the ground-state partners [1]. [Pg.42]

This behaviour suggests that carotenoids not only remove the toxic singlet oxygen but can also neutralize the energy excess that is transferred from chlorophyll to molecular oxygen [1,125],... [Pg.63]

Here Aft is the electrochemical - supersaturation and G>(n) takes into consideration the total energy excess due to the creation of new interfaces when a nucleus appears on the electrode surface. The last quantity is expressed as a difference between the Gibbs energy G (n)... [Pg.456]

The vertical excitation into the tttt state (S2) amounts to 4.97 eV. Therefore, from an energetic point of view two MXSs are available with the existing energy excess. Since the Sx and S2 states are quite close it can be supposed that in the... [Pg.218]

Figure 13-8. Relevant schematic potential energy curves for the near UV photophysics of the most stable tautomers of guanine. The region of the first singlet tht excited state surface accessible by Franck-Condon excitation is indicated in bold. Excited state internal conversion through a conical intersection (Cl) with S0 is illustrated by curved arrows. Vertical arrows indicate fluorescence emission. The eventual role of excited nir singlet states cannot be ruled out, especially at high energy excess in the excited state (see text)... Figure 13-8. Relevant schematic potential energy curves for the near UV photophysics of the most stable tautomers of guanine. The region of the first singlet tht excited state surface accessible by Franck-Condon excitation is indicated in bold. Excited state internal conversion through a conical intersection (Cl) with S0 is illustrated by curved arrows. Vertical arrows indicate fluorescence emission. The eventual role of excited nir singlet states cannot be ruled out, especially at high energy excess in the excited state (see text)...

See other pages where Energy excessive is mentioned: [Pg.323]    [Pg.465]    [Pg.312]    [Pg.146]    [Pg.190]    [Pg.144]    [Pg.151]    [Pg.262]    [Pg.261]    [Pg.372]    [Pg.151]    [Pg.387]    [Pg.661]    [Pg.277]    [Pg.216]    [Pg.455]    [Pg.12]    [Pg.213]    [Pg.29]    [Pg.278]    [Pg.250]    [Pg.181]    [Pg.35]    [Pg.351]    [Pg.17]    [Pg.299]   
See also in sourсe #XX -- [ Pg.516 ]




SEARCH



Activation energy excess

Activity coefficient from excess Gibbs energy

Activity coefficient multicomponent excess Gibbs energy

Activity coefficient-models multicomponent excess Gibbs energy

And excess free energy

Areal surface excess energy

Binary excess Gibbs free energy

Charge excess energy

Computational methods Excess free energy

Correlation functions excess free energy

Density functional theory excess free energy

Dissipation of excess energy

Energy, configurational excess

Excess Gibbs Energy and Activity Coefficient Equations

Excess Gibbs energy

Excess Gibbs energy Margules

Excess Gibbs energy Margules equations for

Excess Gibbs energy NRTL equation for

Excess Gibbs energy Porter equation for

Excess Gibbs energy Redlich/Kister

Excess Gibbs energy This page has been reformatted by Knovel to provide easier navigation

Excess Gibbs energy UNIQUAC

Excess Gibbs energy Wilson

Excess Gibbs energy Wilson equations for

Excess Gibbs energy and the activity coefficient

Excess Gibbs energy empirical expressions for

Excess Gibbs energy equivalent

Excess Gibbs energy equivalent activity coefficients

Excess Gibbs energy local-composition expressions for

Excess Gibbs energy models

Excess Gibbs energy of an ideal dilute solution

Excess Gibbs energy terms Links

Excess Gibbs energy van Laar equations for

Excess Gibbs free energy

Excess Gibbs free energy Margules

Excess Gibbs free energy local composition

Excess Gibbs free energy of mixing

Excess Gibbs-energy Methods

Excess activation free energy

Excess binding energy

Excess compressibility free energy

Excess energies, alloys

Excess energy

Excess energy

Excess energy definition

Excess energy localization

Excess energy model

Excess excitation energy

Excess free energy interaction parameter

Excess free energy of compound

Excess integral molar free energy

Excess interfacial free energy

Excess internal energy

Excess of Internal Energy Caused by Inelastic Collisions

Excess of electronic energy

Excess properties Gibbs energy

Excess surface energy

Excess surface free energy

Excess thermodynamic function internal energy

Excess thermodynamic functions energy

Excess thermodynamic functions free energy

Explicit Expression for the Excess Free Energy

Free energy excess

Gibbs energy excess function

Gibbs energy excess mixing

Gibbs energy excess-property relation

Helmholtz free energy excess

Index excess energy dependence

Margules expression, excess free energy

Micelle excess free energy

Mixing Rules from Models for Excess Gibbs Energy

Mixing excess free energy, binary

Mixing, enthalpy excess Gibbs free energy

Mixtures molecular excess free energy

Molecular excess free energy

Partial molar excess free energy

Potential energy, excess

Pressure on the Excess Free Energy

Regular solution excess Gibbs energy

Several Activity Coefficient (Excess Free-Energy) Models

Solvation, surface excess free energy

Specific excess surface energies

Surface excess Helmholtz free energy

Surface excess internal energy

Thermodynamics excess Gibbs energy

© 2024 chempedia.info