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Ionic entropies single

He also showed that the values of the single ion B s could be related to the ionic entropies. [Pg.599]

Scheme 1.1 The molecular information system modeling the chemical bond between two basis functions /=(o,b) and its entropy/information descriptors. In Panel b, the corresponding nonbonding (deterministic) channel due to the lone-pair hybrid 6° is shown. For the molecular input p = (P, Q), the orbital channel of Panel a gives the bond entropy-covalency represented by the binary entropy function H[P). For the promolecular input p° = (1/2,1/2), when both basis functions contribute a single electron each to form the chemical bond, one thus predicts H[p°] = 1 and the bond information ionicity / = 1 — H(P). Hence, these two bond components give rise to the conserved (P-independent) value of the single overall bond multiplicity N = I + S = 1. Scheme 1.1 The molecular information system modeling the chemical bond between two basis functions /=(o,b) and its entropy/information descriptors. In Panel b, the corresponding nonbonding (deterministic) channel due to the lone-pair hybrid 6° is shown. For the molecular input p = (P, Q), the orbital channel of Panel a gives the bond entropy-covalency represented by the binary entropy function H[P). For the promolecular input p° = (1/2,1/2), when both basis functions contribute a single electron each to form the chemical bond, one thus predicts H[p°] = 1 and the bond information ionicity / = 1 — H(P). Hence, these two bond components give rise to the conserved (P-independent) value of the single overall bond multiplicity N = I + S = 1.
Alot of information about the free energies of transfer of single ions between pure solvents has been accumulated. Less numerous are determinations in mixed solvents, and the ionic enthalpies of transfer and entropies of transfer as function of mole fraction are known as an exception only. In Table 1 ions and solvent mixtures are listed for which free energies of transfer and some other thermodynamic quantities have been determined. [Pg.111]

Module[ dGzero, dHzero, zl, nH ( This program is used to calculate the standard entropy of formation of the single species of a reactant in kj K -1 mol -1 at 298.15 K and zero ionic strength. The reactant name should be in quotation marks. The output is a 1x4 matrix. ) dGzero, dHzero, zi, nH =Transpose[speciesmat] ... [Pg.367]

A single homogeneous phase such as an aqueous salt (say NaCl) solution has a large number of properties, such as temperature, density, NaCl molality, refractive index, heat capacity, absorption spectra, vapor pressure, conductivity, partial molar entropy of water, partial molar enthalpy of NaCl, ionization constant, osmotic coefficient, ionic strength, and so on. We know however that these properties are not all independent of one another. Most chemists know instinctively that a solution of NaCl in water will have all its properties fixed if temperature, pressure, and salt concentration are fixed. In other words, there are apparently three independent variables for this two-component system, or three variables which must be fixed before all variables are fixed. Furthermore, there seems to be no fundamental reason for singling out temperature, pressure, and salt concentration from the dozens of properties available, it s just more convenient any three would do. In saying this we have made the usual assumption that properties means intensive variables, or that the size of the system is irrelevant. If extensive variables are included, one extra variable is needed to fix all variables. This could be the system volume, or any other extensive parameter. [Pg.338]

Tabulated are single-ion entropies of about 110 diatomic and polyatomic ions in water Gibbs energies, enthalpies, and entropies of hydration of monatomic ions at 25 C partial molar volumes of about 120 common ions at 25 C ionic partial molar heat capacities of ions Gibbs energies of transfer of inorganic electrolytes from HjO to 020 and calorimetrically determined enthalpies of solution of salts in H2O and 020. [Pg.756]

In the liquid crystalline phase, molecules exist in one of an enormous number of conformational states, and they are constantly and rapidly undergoing restrac-turing among these different conformations. Busico et al. [13] proposed an electrostatic model for both the mesomorphic phase and the isotropic Uquid of ionic single-chain surfactants. They concluded that the electrostatic energy alone would mainly account for the stability of the mesomorphic state, because the conformational entropy of the alkyl chains is substantially the same in both states and the residual translational and orientational entropy of a mesomorphic liquid is low. [Pg.457]

Desalination of water is a process in which the ionic content of the water is danixed, and thns the entropy of the system decreases. This implies that we always need an energy inpnt. Desalination implies that we go from a single starting solution (brackish water, volume flow rate (j) , , salt concentration CjJ to at least two separate product streams, one being the fresh (dilnte) water ((l) , c ), and the other being the concentrate, or brine (( )voi,c the two product streams are separated in time... [Pg.448]

Instead of continuous modulation, single thermal pulses have been imposed by laser beams. This can be seen as a continuation and an expansion of the temperature-jump technique which had been introduced to study kinetics of ionic processes [36]. The method has found application preferably with single-crystal electrodes [65-70]. Many fundamental quantities have been determined, among them the potential of zero charge (Fpzc) of Au(l 11) [65], the potential of maximum entropy [66, 70], the process of hydrogen adsorption at platinum surfaces [67, 68] and the entropy of double-layer formation [69]. This quantity also has been... [Pg.63]


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