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Transition Point Cells

Another application of the electromotive force method of investigating equilibria is the determination of transition points of allotropic modifications or of different salt hydrates. Investigations of this kind have been carried out by Cohen and others. A cell of the form [Pg.349]

IOH2O NagSO -h IOH2O was determined by Cohen in this way by means of the cell [Pg.349]

10H2O Na2SO saturated saturated Digitized by Microsoft (i) [Pg.349]

Cohen determined the transition temperature for the white and gray modifications of tin by this method. He also investigated the variation with pressure of the transition temperature of the hydrates of zinc sulphate f by subjecting the galvanic cell to various pressures up to 1500 atm., and determining the vanishing point of the e.m.f. by varying the temperature at each pressure. [Pg.350]

In this way he showed that the variation of the transition temperature with pressure is in close agreement with the thermodynamical formula (deduced in Chapter VII. p. 221) for the dependence of the melting point and the transition point on [Pg.350]


Finally, the use of the constant pressure minimization algorithm allows searching for phenomena that can be considered as precursors of pressure-induced transitions. For example, the predicted behaviour of the anatase cell constants as a function of pressure shows that the a(P) and c(P) plots are only linear for P<4 GPa, the value that is close to both the theoretical and experimental transition pressures. At higher pressures the a constant starts to grow under compression, indicating inherent structural instability. In the case of ratile there is a different precursor effect, nami y at 11 GPa the distances between the titanium atom and the two different oxygens, axial and equatorial, become equal. Once again, the pressure corresponds closely to the phase transition point. [Pg.22]

Modifications separated by a second-order transition can never be coexistent. One typical second-order transition, the displacive structural transition, is characterized by the distortion of bonds rather than their breaking, and the structural changes that occur are usually small. Typically, there is continuous variation in the positional parameters and the unit cell dimensions as a function of temperature. The structural changes in the system occur gradually as the system moves away from the transition point. As well as a structural similarity, a symmetry relationship... [Pg.31]

Fig. 13.2. Cytologic features of M phase. M phase is divided into the mitotic phases shown, based on characteristic cytologic features. The transition from metaphase to anaphase is an important control point. Cells may stop and pause before this control point. If the control point is crossed, M phase is concluded with cell division. Fig. 13.2. Cytologic features of M phase. M phase is divided into the mitotic phases shown, based on characteristic cytologic features. The transition from metaphase to anaphase is an important control point. Cells may stop and pause before this control point. If the control point is crossed, M phase is concluded with cell division.
Liver regeneration takes place in three phases (7.) pre-replicative phase, with preparation for mitosis, (2.) proliferative phase, with wave-like mitoses at 6—8 hour intervals, and (3.) restitution phase, with reconstitution of the hver structure. There are two stages to this whole process (7.) priming, which is the transition of latent hepatocytes (Go) into the mitotic cycle (Gp — this reversible process is triggered by cytokines, hormones or other permissive substances, whereby the cells proliferate due to stimulation by the growth factor (2.) progression is the transition from Gi to DNA synthesis (S) — this transition point from Gi to S is marked by the expression of cyclin Di. [Pg.402]

Figure 5.21a presents, on a logarithmic scale, the anodic CTs calculated on a theoretical basis, with and without considering the interaction between lithium ions in the Lii 8Mn2O4 electrode under the cell-impedance-controlled constraint with the conversion factor/= 0.2 at the potential step across the disorder-order and backward transition points. In the case when no interaction is assumed, the theoretical CT does not display any transition time, but rather shows a monotonic increase of its slope from an almost flat value to one of infinity. [Pg.169]

Figure 2. The volumetric thermal expansion of ND4NO4, given as specific cell volume versus temperature, over the temperature range from 10 to 393 K. The dashed line indicates the IV-II transition. The magnitude of the volumetric change at each transition point is also included. Reproduced with permission from Ref. [4]. Figure 2. The volumetric thermal expansion of ND4NO4, given as specific cell volume versus temperature, over the temperature range from 10 to 393 K. The dashed line indicates the IV-II transition. The magnitude of the volumetric change at each transition point is also included. Reproduced with permission from Ref. [4].
ZZ are two zinc electrodes immersed in the solution the cell is placed in a thermostat and the zinc electrodes connected udth a galvanometer. Since at temperatures below the transition point the solubility of the hexahydrate (the metastable form) is greater than that of the heptahydrate, a current will be produced, flowing in the cell from heptahydrate to hexahydrate. As the temperature is raised towards the transition point, the solubilities of... [Pg.313]

Humidity and Heat. Moisture is crucial to the normal behaviour of cellulosic fibres. Under moderate conditions (relative humidity 45-65%) water is readily absorbed through the network of pores running through a fibre cell, it coats cellulose crystallites and acts as a plasticiser of the amorphous regions, disrupting inter-chain hydrogen bonds. Without this bound water the fibre would be permanently brittle, with an effective glass transition point way above room temperature. [Pg.67]

In the following sections we describe critical experiments that led to the current model of eukaryotic cell-cycle regulation summarized in Figure 21-2 and present further details of the various regulatory events. As we will see, results obtained with different experimental systems and approaches have provided insights about each of the key transition points in the cell cycle. For historical reasons, the names of various cyclins and cyclln-dependent kinases from yeasts and vertebrates differ. Table 21-1 lists the names of those that we discuss in this chapter and indicates when in the cell cycle they are active. [Pg.858]

FIGURE 41.8 Representative stress-strain curve for a cellular solid. The plateau region for compression in the case of elastomeric foam (a rubbery polymer) represents elastic buckling for an elastic-plastic foam (such as metallic foam), it represents plastic yield, and for an elastic-brittle foam (such as ceramic) it represents crushing. On the tension side, point A represents the transition between cell wall bending and cell wall alignment In elastomeric foam, the alignment occurs elastically, in elastic plastic foam it occurs plastically, and an elastic-brittle foam fractures at A. [Pg.665]

In the a a phase transition at temperatures and hydrogen pressures below 293°C and 2 MPa, respectively, the lattice expands at the phase transition point increasing in volume by about 10% [22]. This unit cell volume change can result in mechanical strains, physical distortions, and possibly failure of the palladium if cycled through the palladium hydride phase transition region. [Pg.64]


See other pages where Transition Point Cells is mentioned: [Pg.260]    [Pg.198]    [Pg.234]    [Pg.24]    [Pg.36]    [Pg.799]    [Pg.285]    [Pg.293]    [Pg.409]    [Pg.144]    [Pg.272]    [Pg.457]    [Pg.32]    [Pg.51]    [Pg.183]    [Pg.207]    [Pg.198]    [Pg.534]    [Pg.349]    [Pg.360]    [Pg.79]    [Pg.1018]    [Pg.414]    [Pg.34]    [Pg.139]    [Pg.573]    [Pg.97]    [Pg.280]    [Pg.313]    [Pg.198]    [Pg.2]    [Pg.214]    [Pg.71]    [Pg.150]    [Pg.626]    [Pg.352]    [Pg.452]   


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