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Reaction, heat free energy

STANDARD HEAT OF REACTION, STANDARD FREE-ENERGY CHANGE, AND EQUILIBRIUM CONSTANT 1.67... [Pg.2]

The equilibrium constants above can be calculated from heat/free energy of formation data based on the pure component standard states at A = 1 atm and the temperature of interest. These results are shown in Figure 1.13. As in Illustration 1.6, we make a table for the extent of reaction based on one mol of steam for the gaseous species. This gives the following set of coupled nonlinear... [Pg.59]

For many polymerization reactions the entropy changes have been either measured or calculated, and from these, combined with the measured heats of reaction, the free energies of polymerization can be calculated. From these data it is possible to determine the extent to which polymerization occurs, and the relative influence of the heat and entropy effects on the reaction equilibrium. [Pg.86]

The overall enzyme-catalysed reaction succeeds in three steps formation of the enzyme-substrate complex, conversion of the complex to an enzyme-product complex, and dissociation of the enzyme-product complex to products and free enzyme. There are at least 18 thermodynamic parameters for the forward reaction, i.e., the heat, free energy and entropy of activation, and the heat, free energy and entropy of the process for each of these stages. [Pg.311]

Heat capacity, latent heat, ionic conductivity, enthalpy, entropy Viscosity, thermal conductivity, diffusion coefficients Equilibrium constants, association/dissociation constants, enthalpy of formation, enthalpy of combustion, heat of reaction, Gibbs free energy of formation, reaction rates Surface tension... [Pg.299]

Gibbs-Helmholtz equation This equation relates the heats and free energy changes which occur during a chemical reaction. For a reaction carried out at constant pressure... [Pg.190]

Free energy is related to two other energy quantities, the enthalpy (the heat of reaction measured at constant pressure) and the entropy. S. an energy term most simply visualised as a measure of the disorder of the system, the relationship for a reaction taking place under standard conditions being... [Pg.66]

Thermodynamics of Chemical Reactions 95 Heats and Free Energies of Formation (continued)... [Pg.95]

Thermodynamic data Data associated with the aspects of a reaction that are based on the thermodynamic laws of energy, such as Gibbs free energy, and the enthalpy (heat) of reaction. [Pg.1017]

Usually, only the Arrhenius energy of activation, E, is given in these papers it differs from the heat of activation,JH, by RT (about 0.6 kcal at ordinary temperatures). Only a few entropies of activa-tion, JS, were calculated the frequency factor, whose logarithm is tabulated, is proportional to this reaction parameter. It is clear that the rate, E, and JS determined for an 8jfAr2 reaction are for the overall, two-stage process. Both stages will contribute to the overall results when their free energies of activation are similar. [Pg.278]

The production of ammonia is of historical interest because it represents the first important application of thermodynamics to an industrial process. Considering the synthesis reaction of ammonia from its elements, the calculated reaction heat (AH) and free energy change (AG) at room temperature are approximately -46 and -16.5 KJ/mol, respectively. Although the calculated equilibrium constant = 3.6 X 108 at room temperature is substantially high, no reaction occurs under these conditions, and the rate is practically zero. The ammonia synthesis reaction could be represented as follows ... [Pg.144]

For the electrochemical cell reaction, the reaction free energy AG is the utilizable electrical energy. The reaction enthalpy AH is the theoretical available energy, which is increased or reduced by an amount TAS. The product of the temperature and the entropy describes the amount of heat consumed or released reversibly during the reaction. With tabulated values for the enthalpy and the entropy it is possible to obtain AG. ... [Pg.10]

The reversible reaction heat of the cell is defined as the reaction entropy multiplied by the temperature [Eq. (15)]. For an electrochemical cell it is also called the Peltier effect and can be described as the difference between the reaction enthalpy AH and the reaction free energy AG. If the difference between the reaction free energy AG and the reaction enthalpy AH is below zero, the cell becomes warmer. On the other hand, for a difference larger than zero, it cools down. The reversible heat W of the electrochemical cell is therefore ... [Pg.12]

The relation between reaction free energy, temperature, cell voltage, and reversible heat in a galvanic cell is reflected by the Gibbs-Helmholtz equation [Eq. (31)]. [Pg.13]

For a reaction 2 ia == 0 between condensed substances with evolution of heat [Q], we have for the maximum work, i.e.f the loss of free energy ... [Pg.532]

T. W. Richards, The Significance of Changing Atomic Volume 111. The Relation of Changing Heat Capacity to Change of Free Energy. Heat of Reaction. Change of Volume, and Chemical Affinity". Z. Physik. Chem. 42. 129-154 (1902). [Pg.201]


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