Crystal nucleation temperature

Scaling is not always related to temperature. Calcium carbonate and calcium sulfate scaling occur on unheated surfaces when their solubiUties are exceeded in the bulk water. Metallic surfaces are ideal sites for crystal nucleation because of their rough surfaces and the low velocities adjacent to the surface. Corrosion cells on the metal surface produce areas of high pH, which promote the precipitation of many cooling water salts. Once formed, scale deposits initiate additional nucleation, and crystal growth proceeds at an accelerated rate. 

Crystal Morphology. Size, shape, color, and impurities are dependent on the conditions of synthesis (14—17). Lower temperatures favor dark colored, less pure crystals higher temperatures promote paler, purer crystals. Low pressures (5 GPa) and temperatures favor the development of cube faces, whereas higher pressures and temperatures produce octahedral faces. Nucleation and growth rates increase rapidly as the process pressure is raised above the diamond—graphite equiUbrium pressure. 

As can be seen from Fig. 6, liquid-liquid demixing clearly precedes crystallization in case Cl. Moreover, crystallization in this case occurs at a higher temperature than in cases C2 and C3. Apparently, the crystallization takes place in the dense disordered phase (which has a higher melting temperature than the more dilute solution Fig. 5). In case C2, the crystallization temperature is close to the expected critical point of liquid-liquid demixing, but higher than in case C3. This suggests that even pre-critical density fluctuations enhance the rate of crystal nucleation. 

As described above, Ryan and coworkers [29-31] have shown very clearly the phenomenon of the so-called SAXS before WAXD, that is, that an induction period exists where larger density fluctuations begin before crystal nucleation. They also used iPP samples and crystallized them at high temperatures between 130 °C and 142 °C, to ensure that the crystallization is... 

On the basis of the concept described above, we propose a model for the homogeneous crystallization mechanism of one component polymers, which is schematically shown in Fig. 31. When the crystallization temperature is in the coexistence region above the binodal temperature Tb, crystal nucleation occurs directly from the melt, which is the well-known mechanism of polymer crystal nucleation. However, the rate of crystallization from the coexistence region is considered to be extremely slow, resulting in single crystals in the melt matrix. Crystallization at a greater rate always involves phase separation the quench below Tb causes phase separations. The most popular case... 

Turnbull and Cech [58] analyzed the solidification of small metal droplets in sizes ranging from 10 to 300 xm and concluded that in a wide selection of metals the minimum isothermal crystallization temperature was only a function of supercooling and not of droplet size. Later, it was found that the frequency of droplet nucleation was indeed a function of not only crystallization temperature but also of droplet size, since the probability of nucleation increases with the dimension of the droplet [76]. However, for low molecular weight substances the size dependence of the homogeneous nucleation temperature is very weak [77-80]. 

We have represented schematically in Fig. 5, the maximum temperature range that can be associated with homogeneous nucleation temperatures for PEO. Some data, where Avrami indexes of 1 or lower have been reported, have crystallization temperatures that fall above this range, so they should not be associated with homogeneous nucleation. Another origin for the low Avrami indexes may be involved in these cases. 

Fig. 18 Peak crystallization temperature as a function of self-nucleation temperature for hydrogenated and nonhydrogenated S27B15C58 triblock copolymers. (Reprinted with permission from [97]. Copyright 1998 American Chemical Society)...

The effective secondary nucleation rate of alumina trihydrate in a batch crystallizer for temperature 55 to 70 C is given by ... 

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