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Solid state significance

Liquid-phase sintering is significantly more complex tlian solid-state sintering in tliat tliere are more phases, interfaces, and material transport mechanisms to consider. In general, densification will occur as long as it is... [Pg.2770]

Three-body and higher terms are sometimes incorporated into solid-state potentials. The Axilrod-Teller term is the most obvious way to achieve this. For systems such as the alkali halides this makes a small contribution to the total energy. Other approaches involve the use of terms equivalent to the harmonic angle-bending terms in valence force fields these have the advantage of simplicity but, as we have already discussed, are only really appropriate for small deviations from the equilibrium bond angle. Nevertheless, it can make a significant difference to the quality of the results in some cases. [Pg.257]

Transformations in the Solid State. From a practical standpoint, the most important soHd-state transformation of PB involves the irreversible conversion of its metastable form II developed during melt crystallization into the stable form I. This transformation is affected by the polymer molecular weight and tacticity as well as by temperature, pressure, mechanical stress, and the presence of impurities and additives (38,39). At room temperature, half-times of the transformation range between 4 and 45 h with an average half-time of 22—25 h (39). The process can be significantly accelerated by annealing articles made of PB at temperatures below 90°C, by ultrasonic or y-ray irradiation, and by utilizing various additives. Conversion of... [Pg.427]

Studies of cyclodecane derivatives by X-ray crystallographic methods have demonstrated that the boat-chair-boat conformation is adopted in the solid state. (Notice that boat is used here in a different sense than for cyclohexane.) As was indicated in Table 3.7 (p. 146), cyclodecane is significantly more strained than cyclohexane. Examination of the boat-chair-boat conformation reveals that the source of most of this strain is the close van der Waals contacts between two sets of three hydrogens on either side of the molecule. [Pg.148]

Intermetallics also represent an ideal system for study of shock-induced solid state chemical synthesis processes. The materials are technologically important such that a large body of literature on their properties is available. Aluminides are a well known class of intermetallics, and nickel aluminides are of particular interest. Reactants of nickel and aluminum give a mixture with powders of significantly different shock impedances, which should lead to large differential particle velocities at constant pressure. Such localized motion should act to mix the reactants. The mixture also involves a low shock viscosity, deformable material, aluminum, with a harder, high shock viscosity material, nickel, which will not flow as well as the aluminum. [Pg.184]

This chapter presents detailed and thorough studies of chemical synthesis in three quite different chemical systems zinc ferrite, intermetallic, and metal oxide. In addition to different reaction types (oxide-oxide, metal-metal, and metal oxide), the systems have quite different heats of reaction. The oxide-oxide system has no heat of reaction, while the intermetallic has a significant, but modest, heat of reaction. The metal oxide system has a very large heat of reaction. The various observations appear to be consistent with the proposed conceptual models involving configuration, activation, mixing, and heating required to describe the mechanisms of shock-induced solid state chemistry. [Pg.194]

This book has certainty not included all observations of solid state physical and chemical processes that have been carried out over the past 40-yr history of shock compression science, but has necessarily emphasized those studies in which the author has made significant contributions. Other independent studies reinforce these observations. [Pg.198]

Hua Li, Nai-Ben Ming. Significance of many-body interactions in Monte Carlo simulation of crystal-vapour interface. Solid State Commun 707 351, 1997. [Pg.932]


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See also in sourсe #XX -- [ Pg.49 , Pg.54 , Pg.60 , Pg.66 , Pg.81 , Pg.82 ]




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