Enthalpy alloys

Reviews of batch calorimeters for a variety of applications are published in the volume on Solution Calorimetry [8] cryogenic conditions by Zollweg [22], high temperature molten metals and alloys by Colinet andPasturel [19], enthalpies of reaction of inorganic substances by Cordfunke and Ouweltjes [16], electrolyte... 

The tables in this section contain values of the enthalpy and Gibbs energy of formation, entropy, and heat capacity at 298.15 K (25°C). No values are given in these tables for metal alloys or other solid solutions, for fused salts, or for substances of undefined chemical composition. 

There is a lively controversy concerning the interpretation of these and other properties, and cogent arguments have been advanced both for the presence of hydride ions H" and for the presence of protons H+ in the d-block and f-block hydride phases.These difficulties emphasize again the problems attending any classification based on presumed bond type, and a phenomenological approach which describes the observed properties is a sounder initial basis for discussion. Thus the predominantly ionic nature of a phase cannot safely be inferred either from crystal structure or from calculated lattice energies since many metallic alloys adopt the NaCl-type or CsCl-type structures (e.g. LaBi, )S-brass) and enthalpy calculations are notoriously insensitive to bond type. 

M. Migschitz and W Pfeiler, Vacancy activation enthalpies of Au-Fe alloys determined from SRO-induced resistivity changes, A/a/. Sci. Eng. A206 I55 (1996)... 

The partial molar entropy of a component may be measured from the temperature dependence of the activity at constant composition the partial molar enthalpy is then determined as a difference between the partial molar Gibbs free energy and the product of temperature and partial molar entropy. As a consequence, entropy and enthalpy data derived from equilibrium measurements generally have much larger errors than do the data for the free energy. Calorimetric techniques should be used whenever possible to measure the enthalpy of solution. Such techniques are relatively easy for liquid metallic solutions, but decidedly difficult for solid solutions. The most accurate data on solid metallic solutions have been obtained by the indirect method of measuring the heats of dissolution of both the alloy and the mechanical mixture of the components into a liquid metal solvent.05... 

Preliminary work by solution calorimetry (Oriani and Murphy, to be published) shows clearly that the enthalpy of formation of solid Co-Pt alloys is a negative quantity, so that the statement made on p. 125 is not correct. 

Lead, excess entropy of solution of noble metals in, 133 Lead-thalium, solid solution, 126 Lead-tin, system, energy of solution, 143 solution, enthalpy of formation, 143 Lead-zinc, alloy (Pb8Zn2), calculation of thermodynamic quantities, 136 Legendre expansion in total ground state wave function of helium, 294 Lennard-Jones 6-12 potential, in analy-... 

Platinum-cobalt alloy, enthalpy of formation, 144 Polarizability, of carbon, 75 of hydrogen molecule, 65, 75 and ionization potential data, 70 Polyamide, 181 Poly butadiene, 170, 181 Polydispersed systems, 183 Polyfunctional polymer, 178 Polymerization, of butadiene, 163 of solid acetaldehyde, 163 of vinyl monomers, 154 Polymers, star-shaped, 183 Polymethyl methacrylate, 180 Polystyrene, 172 Polystyril carbanions, 154 Potential barriers of internal rotation, 368, 374... 

ZEBRA 567 energy efficiency 15 enhancement factor, lithium alloys 367 enhancing cation mobility 518 enthalpy 9... 

Hess s law A reaction enthalpy is the sum of the enthalpies of any sequence of reactions (at the same temperature and pressure) into which the overall reaction can be divided, heterogenous alloy See alloy. heterogeneous catalyst See catalyst. heterogeneous equilibrium An equilibrium in which at least one substance is in a different phase from the others. Example AgCI(s) Ag+(aq) + Cl "(aq). heterogeneous mixture A mixture in which the... 

Lattice constants for Pd-Rh alloys quenched from 1300°C vary smoothly with composition, showing only a small positive deviation from Vegard s law, but prolonged vacuum annealing below 850°C revealed the existence of a wide miscibility gap 151). Figure 25 shows the limits of the miscibility gap calculated from the lattice constants of the two-phase system between 825° and 600°C. Recent thermodynamic data (Table I) confirm the tendency to phase separation. The enthalpies of formation are endothermic... 

In metals the electrons lose their association with individual atoms and the number of valence electrons is often used in rationalization schemes. Estimated enthalpies of formation for equi-atomic alloys, MM, of two elements of the first transition metal series are given as a function of the difference in number of valence electrons in Figure 7.13 [8], Compounds of a given common metal are given a specific symbol. For example, the scandium compounds ScM where M = Ti, V, Cr, Mn, Fe, Co, Ni and Zn, are given by open circles. The metal M of the compound MM is... 

Data for Mo and W compounds (MoM and WM ) are included in Figure 7.13 to show the effect of going from one period to the next. The variation in enthalpy of formation with the difference in number of valence electrons is similar however, the enthalpies of formation are more exothermic for the MoM and WM compounds compared with the corresponding first transition metal series element compounds CrM. Finally, it should be added that the enthalpies of formation of equiatomic alloys of elements of the same group are close to zero. 

Enthalpies of formation of metallic compounds and alloys can also be determined directly through reactions such as [60] ... 

The fundamental issues to be addressed in the process modeling include spray enthalpy, gas consumption, spray mass distribution, microstructure of solidified droplets, and droplet-substrate interactions. The effects of atomization gas chemistry, alloy composition and operation conditions on the resultant droplet properties are also to be investigated in the process modeling. 

In the same chapter (Chapter 5), as an introduction to the paragraphs dedicated to the various groups of metals, the values relevant to a number of elementary properties have been collected. These are atomic properties (such as metallic and ionic radii, ionization energies, electronegativities, Mendeleev number, chemical scale, Miedema parameters, etc.), crystal structure and lattice parameters data of the allotropes of the elements, and selected thermodynamic data (melting and boiling temperatures and enthalpies, etc.). All these data indeed represent reference values in the discussion of the alloying behaviour of the elements. 

The Miedema s parameters and the Miedema model and formula proved to be useful in an approximate evaluation of the formation enthalpy of alloys, in the estimate of the formation capability of intermetallic compounds, etc. 

Miedema s model and parameters and prediction of compound formation capability. A semi-empirical approach to the evaluation of the compound formation capability and of the heats of formation of alloys was proposed by Miedema and co-workers. This resulted in a model which became very popular and, especially because there was scarcity of experimental data, was frequently used in the evaluation, even if approximate and several times incorrect, of the formation enthalpies. The model suggested for energy effects in alloys is well known essentially it is based on the definition of two parameters. By assigning two coordinates... 

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