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Crystal growth theories

The classical crystal growth theory goes back to Burton, Cabrera and Frank (BCF) (1951). The BCF theory presents a physical picture of the interface (Fig. 6.9c) where at kinks on a surface step - at the outcrop of a screw dislocation-adsorbed crystal constituents are sequentially incorporated into the growing lattice. [Pg.233]

Lower et al. (1998b) can shed more light on this phenomenon. They again used AFM, SEM, TEM, SEM-EDS, electron diffraction, and XRD to study the reactions between 0.5 and 500 mg/L of Pb with hydroxyapatite at pH 6 and a reaction temperature of 22 °C. A commercial hydroxyapatite was used at sorbent concentrations of 0.5 g/L. Reactions were observed over a 2 h period. At high initial Pb concentrations, Pb solution concentrations dropped from 500 mg/L to <100 mg/L. At concentrations of 0.5-100 mg Pb/L, after reaction, Pb levels dropped to less than 15 pg/L. In both cases, hydroxyapatite dissolved and hydroxypyromorphite formed. The authors applied some nucleation and crystal growth theory developed... [Pg.445]

He started to work at the Chemical Faculty of Sofia University where he became a professor and the head of the Department of Physical Chemistry, in 1947. Kaishev founded the Institute of Physical Chemistry of the Bulgarian Academy of Sciences in 1958, and helped to establish the Central Laboratory of Electrochemical Power Sources [i]. Kaishev started to collaborate with - Stran-ski in Berlin in 1931 [iii] and became his assistant in Sofia in 1933. They laid the fundamentals of the crystal growth theory. They proposed the first kinetic theory of the two-dimensional nucleation and growth. The spiral type growth during electrocrystallization was first observed by Kaishev on silver [iii]. On the history of the creation of the molecular-kinetic theory of crystal growth see [iv]. [Pg.379]

The conditions for stable growth of a crystal are closely associated with segregation of dopants or impurities. Crystal growth theory includes an expression for the effective segregation coefficient K, for a crystal growing from a medium in which the dopant distribution is characterized by a boundary layer of thickness 5 ... [Pg.103]

C. H. L. Goodman, Crystal Growth Theory and Technique, Vols. 1 and 2, Plenum Press, London, 1974, 1978. [Pg.437]

To address the problem of faceting of grains, we use a classical atomistic approach by reasoning with a Kossel crystal representation, which is commonly used in crystal growth theories. The main idea is summarized as follows ... [Pg.184]

Where do the steps come from and what is the rate controlling factor in determining the crystal growth rate The goal of crystal growth theories is to try to answer these two questions. [Pg.54]

Once a surface nuclei is formed, the next question is how does the nuclei spread to form a complete layer. The simplest crystal growth theory assumes that when a surface nuclei is formed, it spreads across the surface at an infinite velocity. The surface must then await the formation of another surface nuclei. Since the ratedetermining step in this model is the formation of a surface nuclei, the growth rate of the crystal can be expressed as... [Pg.55]

The Chernov bulk diffusion model provides an important link between crystal growth theory and the practical world of industrial crystallization where fluid flow and agitation are important. The effect of hydrodynamics on crystal growth will be discussed in the next section. The Diffusion Layer Model. [Pg.56]

In the previous section, we reviewed a number of different crystal growth theories. These provide a theoretical basis for the correlation of experimental crystal growth data and the determination of kinetic parameters from the data to be used in models of... [Pg.57]

In our discussions of crystal growth theory and kinetics, we have assumed that the crystal growth rate is not a function of crystal size. While a good first assumption, this is not always true. As we saw in our discussion of Ostwald ripening, there is a difference in solubility between very small particles and larger particles. This differential solubility will result in a difference in supersaturation as a function of particle size. The smaller particles will be at a lower supersatura-... [Pg.62]

Crystal growth theories aim to describe how an energetically xmfavorable flat faces grows and how a set... [Pg.364]

For a comprehensive account of the historical development of the many crystal growth theories, reference should be made to the critical reviews by Wells (1946), Buckley (1952), Strickland-Constable (1968), Lewis (1980), Chernov (1980, 1989) and Nyvlt et al. (1985). [Pg.216]

The observed lamellar thickness is, however, always greater than the lamellar thickness calculated from crystal growth theory (Lia Xh r a factor of y ... [Pg.399]

Dove, P.M., Han, N., De Yoreo, II (2005). Mechanisms of classical crystal growth theory explain quartz and silicate dissolution behavior. Proceedings of the National Academy of Sciences, 102, 15357-15362. [Pg.214]

In order to explain experimental results, crystal growth theories have been developed that consider different steps in the growth process as rate limiting. The step that is rate limiting is dependent on the substance being precipitated and the experimental conditions. Most sparingly soluble salts at moderate supersaturation levels (S < 20) have been found to have a parabolic dependence of growth on... [Pg.11]

The phenomenological laws that any crystal growth theory must address are ... [Pg.195]

R. Falckenberg, 1978, in Crystal Growth, Theory and Techniques, (ed.) C.H.L. Goodman, Plenum Press,... [Pg.433]


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