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Surfaces of crystals

Although the structure of the surface that produces the diffraction pattern must be periodic in two dimensions, it need not be the same substance as the bulk material. Thus LEED is a particularly sensitive tool for studying the structures and properties of thin layers adsorbed epitaxially on the surfaces of crystals. [Pg.1368]

Deviations from the Avrami equation are frequently encountered in the long time limit of the data. This is generally attributed to secondary nucleation occurring at irregularities on the surface of crystals formed earlier. [Pg.234]

In the former, the solute diffuses from the bulk of the solution to the external surface of crystals. Molecules of the solute already adsorbed on the surface are then integrated into the crystal lattice. The rate of both steps can be expressed by the equation ... [Pg.239]

Since the surfaces of crystals have specific symmetries (usually triangular, square, or tetragonal) and indenters have cylindrical, triangular, square, or tetragonal symmetries, the symmetries rarely match, or are rotationally misaligned. Therefore, the indentations are often anisotropic. Also, the surface symmetries of crystals vary with their orientations relative to the crystallographic axes. A result is that crystals cannot be fully characterized by single hardness numbers. [Pg.24]

Where is the water located (i.e., adsorbed to the external surface of crystals, absorbed into crystals as specific or nonspecific water of hydration, absorbed into amorphous regions, condensed into pores, etc.) ... [Pg.389]

On the basis of crystallochemistry consideration and taking into account electron microscopy observations of the surface of crystals upon which some polymer was formed,99 Arlman and Cossee13 concluded that the active sites are located on crystal surfaces different from the basal (001) ones. In particular, these authors considered in detail active sites located on crystal surfaces parallel in the direction a — b of the unit cell defined as in Ref. 98. Figure 1.13 illustrates that, if we cut a TiCl3 layer parallel to the direction defined above, which corresponds to the line connecting two bridged Ti atoms, electroneutrality conditions impose that each Ti atom at the surface of the cut be bonded... [Pg.39]

During the secondary drying, the water will be removed which interacts with the solids such that the water cannot crystallize. The water can be bound to the surface of crystals in a crystallized product, or can be included in amorphous product. Pikal et al. [1.59] have listed four statements concerning secondary drying ... [Pg.77]

Chromite crystallization from a melt, or its re-equilibration with a melt, creates an even more reduced boundary layer at the crystal-melt interface as a consequence of the incorporation of Cr " and Fe " relative to divalent ions. The reduced conditions trigger the precipitation of IPGE minerals on the surface of crystallizing chromite that can be later on entrapped during chromite growth (Finnigan etal. 2008). [Pg.199]

Goodwin, E. T. (1939). Electronic states at the surfaces of crystals. Proc. Comb. Phil. Sco. 35, 205-231. [Pg.391]

When crystals of mercury fulminate are heated at lower temperatures the decomposition reaction is localized mainly around lattice defects such as growth marks on the surface of crystals or points where dislocations emerge at the surface (Fig. 32(c)). [Pg.144]

Thus, according to Rogers [117] when the surface of crystals which have been given a flash, but which have not exploded or broken down, is examined by an optical microscope, it can be seen that the crystal is much darkened on the irradiated face, and contains many irregular but parallel cracks. The cracks are not visible on the other side of the crystals suggesting that they penetrate only a short distance into it. [Pg.183]

To determine the effect of adsorption on the secondary porous structure of the pellets and on the external surface of the crystals on their size variation, benzene adsorption was measured. The voids or micropores of the zeolite NaA are inaccessible to benzene molecules. Adsorption occurs only on the external surface of the crystals and in the secondary porous structure formed by the gaps between the contacting zeolite crystals. In Figure 3 the relative pressure is plotted on the z-axis for better comparison. Variations in the sizes of the pellets of zeolite NaA up to p/p9 = 0.93 are negligibly small, and the points coincide with the x-axis. Consequently, adsorption on the external surface of crystals and at the sites of their contact—i.e., in transitional and macropores of the secondary porous... [Pg.407]

AU =15 kcal/gmol (coupled dislocation processes, mobility of molecular segments fixed near the surface of crystals or a process). [Pg.32]

One of the most probable structural features related to e -h+ recombination is crystallinity. It is assumed that the recombination occurs at crystal defects.13) In fact, amorphous Ti02 showed negligible photocatalytic activity, presumably due to the defects in the particles,7) but we have few methods to evaluate the number of defects in photocatalyst powders. Surface of crystals is, in a sense, a defective site, where continuity of crystal structure is terminated, and thereby, the larger the surface area, the faster the recombination. Since the surface area also has a positive influence, i.e., in a reversed way of e -h+ recombination, on the reaction rate of e- and h+ with substrates, estimation of overall photocatalytic activity should be made carefully when the surface reaction predominates the recombination, the photocatalyst of larger surface area is better, and vice versa.14,15)... [Pg.23]

Thus, melting of a crystalline substance without superheating is a superficial effect. Pre-melting phenomena are apparently also related to the formation of liquid films on the surfaces of crystals, if not to other incidental causes (for example, impurities), and are not pertinent to Frenkel s theory. Heterophase fluctuations are quite large where the difference between two phases and the surface tension between them tend to zero—near the critical point and near the Curie point. The first case is commonly known, the second was earlier investigated quantitatively in Landau s fine work [13, 14]. [Pg.130]

S Surface Sorbate sliding or hopping along surface of crystals. Dependent on sorption Isotherm, zeolite and sorbate geometry. [Pg.81]

The discovery of the piezoelectric effect (the appearance of electrical charges on different surfaces of crystals under mechanical stress) in 1880 by Pierre Curie (1859-1906) and his brother Jacques (1855-1941) is discussed in a brief paper.91... [Pg.138]

The VDR behaviour in ZnO varistors is governed by electron states that are formed on the surfaces of crystals as a consequence of the discontinuity. These surface states act as acceptors for electrons from the n-type semiconductor. Electrons will be withdrawn from the region near the surface and replaced by a positive space charge. In this way oppositely oriented Schottky barriers will be created at the surfaces of neighbouring crystals so that a high resistance will be offered to electron flow in either direction (Fig. 4.10(a)). The situation with an applied field is shown in Fig. 4.10(b). With low applied fields small thermally... [Pg.151]

In the / -spectrum of the ZnO thin film, a similar plateau as in the 3 -spectrum of the ZnO bulk sample is present. However, the phonon modes of the sapphire substrate introduce additional features, for example atw 510, 630, and "-900 cm 1 [38,123]. The spectral feature at w 610 cm-1 is called the Berreman resonance, which is related to the excitation of surface polari-tons of transverse magnetic character at the boundary of two media [73]. In the spectral region of the Berreman resonance, IRSE provides high sensitivity to the A (LO)-mode parameters. For (OOOl)-oriented surfaces of crystals with wurtzite structure, linear-polarization-dependent spectroscopic... [Pg.92]

APM) phase velocity of plate wave phase velocity of shear wave jc-component of particle velocity in liquid value of Vjc at surface of crystal three particle velocity ccnnponents at surface (for SAW) propagation velocity (for SAW)... [Pg.401]

Surfaces of crystals and the grain boundaries may have disordered regions where proton transport is facilitated. Adsorbed water or electrolyte solution trapped between the grains will also increase the conductivity and give rise to false conclusions concerning the solid-state nature of conductivity. Surface or liquidlike conductivity has a low activation energy ( a 0.1-0.4eV), approaching the of aqueous acidic... [Pg.1812]


See other pages where Surfaces of crystals is mentioned: [Pg.240]    [Pg.237]    [Pg.123]    [Pg.242]    [Pg.158]    [Pg.472]    [Pg.18]    [Pg.239]    [Pg.111]    [Pg.161]    [Pg.418]    [Pg.91]    [Pg.268]    [Pg.19]    [Pg.579]    [Pg.12]    [Pg.39]    [Pg.147]    [Pg.24]    [Pg.331]    [Pg.433]    [Pg.217]    [Pg.570]    [Pg.234]    [Pg.372]    [Pg.433]    [Pg.520]    [Pg.1770]   


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Ammonia-Induced Restructuring of Iron Single-Crystal Surfaces

Anchoring Effects of Nematic Liquid Crystal at Surfaces

Assembled Monolayers of Metal Complexes on Single-Crystal Surfaces

Bulk Crystallization of Polymers in Contact with a Foreign Surface

Crystal surfaces of platinum

Crystallization of Thin Polymer Films on Amorphous Foreign Surface

Enlargement of single crystal diamond surface area

Epitaxy Involving Fold Surfaces of Polymer Crystals

Hydrogenation of 1,3-Butadiene on Single Crystal Surfaces

Models of crystal surfaces

Structural Investigation of Crystal Surfaces and Structure Dehydration

Structural Investigations of Crystal Surfaces and Chemical Stability

Surface area, of crystals

Surface microtopography of crystal faces

The Single-Crystal Method of Studying Surface Reactions

The structure of single crystal surfaces

Well-Defined Surface Structure and Reconstruction of Single-Crystal Surfaces

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