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Solid-to-liquid transition

The ability of XPD and AED to measure the short-range order of materials on a very short time scale opens the door for surface order—disorder transition studies, such as the surface solid-to- liquid transition temperature, as has already been done for Pb and Ge. In the caseofbulkGe, a melting temperature of 1210 K was found. While monitoring core-level XPD photoelectron azimuthal scans as a function of increasing temperature, the surface was found to show an order—disorder temperature 160° below that of the bulk. [Pg.249]

Melting point describing the temperature at which the solid to liquid transition takes place is one of the main characteristics of chemical substances. When heat is supplied to a crystalline species its temperature usually rises until it starts to melt. This temperature corresponding to the melting point is maintained until all the substance is liquified. During this process the long-range order of the crystalline solid is destroyed. Simultaneously anisotropy of the crystal, that is, a dependence of its optical and some other properties on the direction of, for... [Pg.84]

When an ionic salt such as NaCl melts, the ionic lattice (see Figure 5.15) collapses, but some order is stiU retained. Evidence for this comes from X-ray diffraction patterns, from which radial distribution functions reveal that the average coordination number (with respect to cation-anion interactions) of each ion in liquid NaCl is 4, compared with 6 in the crystalline lattice. For cation-cation or anion-anion interactions, the coordination number is higher, although, as in the solid state, the intemuclear distances are larger than for cation-anion separations. The solid-to-liquid transition is accompanied by an increase in volume of il0-15%. The number of ions in the melt can be determined in a similar way to that described in Section 8.8 for H2SO4 systems in molten NaCl, v = 2. [Pg.227]

Figure 6. Photographs demonstrating the deliquescence ofBGLU in CO2 at 23.0 X (A) solid material (B) in contact with gaseous CO2 at the deliquescence pressure of 55.9 bar undergoing the solid-to-liquid transition as indicated by... Figure 6. Photographs demonstrating the deliquescence ofBGLU in CO2 at 23.0 X (A) solid material (B) in contact with gaseous CO2 at the deliquescence pressure of 55.9 bar undergoing the solid-to-liquid transition as indicated by...
Thermosetting polymers (also called thermosets) are a family of plastics characterized by the fact that they are formed starting from a liquid solution that irreversibly leads to a solid material during a heating step. In this sense, they exhibit an opposite behavior than the one of thermoplastic polymers that, with some exceptions, show a reversible solid-to-liquid transition when heated to a convenient temperature. Although the irreversible liquid-to-solid transition can be also produced by other means such as UV or electron beam irradiation, the resulting products are also called thermosetting polymers. The process by which the initial liquid solution is transformed into a solid is usually known as the cure of the material. [Pg.519]

The critical value of Ab for the solid-to-liquid transition of finite systems has been suggested to be close to 0.1 [132-134]. [Pg.23]

Molecular dynamics has proved to be a powerful method for simulating and/or predicting several features of polymer systems. Properties on either side of the glass transition temperature (see Section 1.5) have been successfully simulated, as has the solid-to-liquid transition, and provided descriptions of the dynamics (segmental motions, chain diffusion, conformational transitions, etc.) that are in accord with relaxation measurements and such bulk properties as shear viscosities and elastic moduli. The method may also provide a good description of the variation in heat capacity and other thermodynamic fimctions across a phase transition. Several collections of these investigations have recently been published. ... [Pg.62]

Strategy At the melting point, liquid and solid benzene are at equilibrium, so AG = 0. From Equation (18.10) we have AG = 0 = AH — TAS or AS = AH/T. To calculate the entropy change for the solid benzene liquid benzene transition, we write A5j,s = AHfaJTf. Here A//f s is positive for an endothermic process, so ASf s is also positive, as expected for a solid to liquid transition. The same procedure applies to the liquid benzene —> vapor benzene transition. What temperature unit should be used ... [Pg.820]

The recoil-free fraction as a function of the temperature for glassforming FeCl2 in methanol is shown in Figure 6.8. A sharp decrease in / at 7 is observed while the increase in / at higher temperatures is due to crystallisation (Simopoulos, Wickman, Kostikas Petrides, 1970). The solid to liquid transition has also been studied in detail (Boyle et al., 1961) and the decrease in / and the increase in absorption linewidth near the melting point have been very clearly observed (Figure 6.9). [Pg.235]

Think About It For the same substance, AS,ap is always significantly larger than A5(,k. The change in number of microstates is always bigger in a liquid-to-gas transition than in a solid-to-liquid transition. [Pg.741]

The cerium—cerium oxide thermochemical cycle is promising due to ceria s stable crystallographic structure, having a cubic fluorite strucmre when reduced to nonstoichiometries of up to 0.25. Also, complications, such as extensive sintering, that arise from solid-to-solid and solid-to-liquid transitions are avoided (Ackermann et al., 2014). Other chemistry considerations are summarized below ... [Pg.653]


See other pages where Solid-to-liquid transition is mentioned: [Pg.67]    [Pg.33]    [Pg.23]    [Pg.59]    [Pg.90]    [Pg.941]    [Pg.413]    [Pg.278]    [Pg.48]    [Pg.108]    [Pg.628]    [Pg.22]    [Pg.192]    [Pg.595]    [Pg.465]    [Pg.280]    [Pg.41]    [Pg.167]    [Pg.95]    [Pg.64]    [Pg.49]    [Pg.40]    [Pg.76]    [Pg.784]    [Pg.292]   
See also in sourсe #XX -- [ Pg.76 ]




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