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Fig. 4.6. Schematic plot of eqn. (4.9) showing how small k and long / give the best zone refining performance. Fig. 4.6. Schematic plot of eqn. (4.9) showing how small k and long / give the best zone refining performance.
P Krauhs. MOLSCRIPT A program to produce both detailed and schematic plots of protein structure. J Appl Crystallogr 24 946-950, 1991. [Pg.312]

Figure 4-318. Schematic plot of the dimensionless torque T, versus he apparent formation strength... Figure 4-318. Schematic plot of the dimensionless torque T, versus he apparent formation strength...
Numerical Observations Figure 3.42 shows a schematic plot of H versus A for A = 8 Af = 5 two dimensional CA. The lattice size is 64 x 64 with periodic boundary conditions. In the figure, the evolution of the single-site entropy is traced for four different transition events. In each case, for a given A, a rule table consistent with that A is randomly chosen and the system is made to evolve for 500 steps to allow transients to die out before H is measured. [Pg.103]

Fig. 3.42 Schematic plot of H versus A for separate runs see text. Fig. 3.42 Schematic plot of H versus A for separate runs see text.
Fig. 31—A schematic plot of friction versus time, illustrating the climbing of the friction coefficient followed by a sudden drop at the time of slip. Fig. 31—A schematic plot of friction versus time, illustrating the climbing of the friction coefficient followed by a sudden drop at the time of slip.
The effects of anelasticity are seen clearly in the strain-time schematic plot of Fig. 7. The time independent strain, 0, occurs immediately as the stress is apphed. The additional strain, o, is associated with stress-induced anelasticity. The total strain, -i- o, is approached exponentially. When the stress is removed the time independent strain is recovered immediately, while the anelastic component relaxes exponentially with a relaxation time constant, k. [Pg.93]

Difficulties can arise when comparing the catalytic activities of different electrodes where slopes b of the plots of current (or logarithm of current) against potential are different. The schematic plots of log i vs. AE shown in Eig. 28.1 refer to the... [Pg.526]

Fig. 1.9 Schematic plot of a basic three-dimensional imaging pulse sequence with frequency encoding along one axis (read), and phase encoding along the two remaining orthogonal directions. The choice of directions is arbitrary, as is the position of the phase gradients within the sequence. Fig. 1.9 Schematic plot of a basic three-dimensional imaging pulse sequence with frequency encoding along one axis (read), and phase encoding along the two remaining orthogonal directions. The choice of directions is arbitrary, as is the position of the phase gradients within the sequence.
Fig. 1.13 Left schematic plot of the distribu- water flowing under laminar conditions in a tion of flow velocities, vz, for laminar flow of a circular pipe the probability density of dis-Newtonian fluid in a circular pipe the max- placements is constant between 0 and imum value of the velocity, occurring in the Zmax = i>ZimaxA, where A is the encoding time center of the pipe, is shown for comparison. of the experiment. Fig. 1.13 Left schematic plot of the distribu- water flowing under laminar conditions in a tion of flow velocities, vz, for laminar flow of a circular pipe the probability density of dis-Newtonian fluid in a circular pipe the max- placements is constant between 0 and imum value of the velocity, occurring in the Zmax = i>ZimaxA, where A is the encoding time center of the pipe, is shown for comparison. of the experiment.
Figure 9-1. Schematic plot of the (4s + 3dz2) and (4s - 3dz2) orbitals of a third-row transition-metal involved in a M-X bond. Figure 9-1. Schematic plot of the (4s + 3dz2) and (4s - 3dz2) orbitals of a third-row transition-metal involved in a M-X bond.
Schematic plot of the reciprocal molar susceptibility vs. temperature... Schematic plot of the reciprocal molar susceptibility vs. temperature...
Kraulis PJ. MOLSCRIPT A Program to Produce Both Detailed and Schematic Plots of Protein Structures. J Appl Crystallogr 1991 24 946-950. [Pg.95]

Example 5.6 Provide illustrative closed-loop time response simulations. Most texts have schematic plots to illustrate the general properties of a feedback system. This is something that we can do ourselves using MATLAB. Simulate the observations that we have made in previous examples. Use a unity feedback system. [Pg.98]

The most important methods of explorative data analysis concern the study of the distribution of the data and the recognition of outliers by boxplots (Fig. 8.18), histograms (Fig. 8.19), scatterplot matrices (Fig. 8.20), and various schematic plots. [Pg.268]

Finally for Cfe(c) 1 the unperturbed (not self-entangled) single-chain re-laxationjust known from good solvent conditions, takes place. S(Q, t)/S(Q, 0) is a universal function of (Q(Q,t)2/3 with Q(Q) = QZ(Q) In Fig 58b a schematic plot of the crossover behavior of the segmental dynamics under 0-conditions is shown. [Pg.111]

Figure 2.5 (a) Schematic plot of surface tension vs. potential according to equation <2.15) and assuming that cations and anions behave in identical manners, (b) Plot of surface charge density vs. potential obtained riu the differentiation of the curve in (a), (c) Plot of differential capacitance vs. potential obtained via the differentiation of the curve in (b). [Pg.48]

Schematic plots of the internal energy versus the reaction coordinate for both primary and secondary insertions and for generic aspecific, syndiospecific, and isospecific model complexes are sketched in Figures 1.11 a,b, and c, respectively. The minima at the centers and at the ends of the energy curves correspond to alkene-free intermediates, including a growing chain with n and n + 1 monomeric units, respectively. Movements from the central minima toward the left and the right correspond to possible reaction pathways leading to primary and secondary insertions, respectively. For the enantioselective complexes the reaction pathways for monomer enantiofaces being... Schematic plots of the internal energy versus the reaction coordinate for both primary and secondary insertions and for generic aspecific, syndiospecific, and isospecific model complexes are sketched in Figures 1.11 a,b, and c, respectively. The minima at the centers and at the ends of the energy curves correspond to alkene-free intermediates, including a growing chain with n and n + 1 monomeric units, respectively. Movements from the central minima toward the left and the right correspond to possible reaction pathways leading to primary and secondary insertions, respectively. For the enantioselective complexes the reaction pathways for monomer enantiofaces being...
Fig. 5 Schematic plot showing reported crystallization temperatures for PEO in the bulk and as a component of block copolymers of varying compositions. The morphology of the PEO block is indicated on the x-axis. The filled bars are for data where isothermal crystallization measurements were performed and Avrami indexes of 1 or less were reported. The horizontal lines indicate the maximum temperature range that can be associated with PEO homogeneous nucleation, see text... Fig. 5 Schematic plot showing reported crystallization temperatures for PEO in the bulk and as a component of block copolymers of varying compositions. The morphology of the PEO block is indicated on the x-axis. The filled bars are for data where isothermal crystallization measurements were performed and Avrami indexes of 1 or less were reported. The horizontal lines indicate the maximum temperature range that can be associated with PEO homogeneous nucleation, see text...
Schematic plot of free energy of formation of clusters from solution as a function of size (number of ions in the cluster). Curve A corresponds to the (thermodynamically) ultimately formed more stable phase, while curve B corresponds to the precursor phase. Schematic plot of free energy of formation of clusters from solution as a function of size (number of ions in the cluster). Curve A corresponds to the (thermodynamically) ultimately formed more stable phase, while curve B corresponds to the precursor phase.
FIGURE 6. Schematic plot of LUMO energies of aromatic compounds and the resulting LUMO from the interaction of the aromatic LUMO and the substituent LUMO37. Energy for the N02 substitutent LUMO is approximated by the EA of nitromethane37. Reprinted with permission from Reference 37. Copyright (1989) American Chemical Society... [Pg.257]

In addition to the acoustical modes and MSo, we observe in the first half of the Brillouin zone a weak optical mode MS7 at 19-20 me V. This particular mode has also been observed by Stroscio et with electron energy loss spectrocopy. According to Persson et the surface phonon density of states along the FX-direction is a region of depleted density of states, which they call pseudo band gap, inside which the resonance mode MS7 peals of. This behavior is explained in Fig. 16 (a) top view of a (110) surface (b) and (c) schematic plot of Ae structure of the layers in a plane normal to the (110) surface and containing the (110) and (100) directions, respectively. Along the (110) direction each bulk atom has six nearest neighbors in a lattice plane, while in the (100) direction it has only four. As exemplified in Fig. 17, where inelastic... [Pg.236]

Figure 2.1 Simplified schematic plots showing the exponential relationship between the current density i and the potential of the electrode, E. (The latter is represented here as being relative to the standard electrode potential of the couple undergoing electromodification for now, the abscissa ( — ) can be thought of as deviation from equilibrium.) Three examples of electron-transfer rate (/feei) are shown (a) (coincident with the y-axis) representing a very fast rate of electron transfer of 10 A cm" (b) representing an average rate of electron transfer of 10 A cm (c) representing a slow rate of electron transfer of 10 A cm . For each trace, T = 298 K and the reaction was symmetrical , i.e. a = 0.5, as defined later in Section 7.5. Figure 2.1 Simplified schematic plots showing the exponential relationship between the current density i and the potential of the electrode, E. (The latter is represented here as being relative to the standard electrode potential of the couple undergoing electromodification for now, the abscissa ( — ) can be thought of as deviation from equilibrium.) Three examples of electron-transfer rate (/feei) are shown (a) (coincident with the y-axis) representing a very fast rate of electron transfer of 10 A cm" (b) representing an average rate of electron transfer of 10 A cm (c) representing a slow rate of electron transfer of 10 A cm . For each trace, T = 298 K and the reaction was symmetrical , i.e. a = 0.5, as defined later in Section 7.5.
Fig. 1.33 Schematic plot showing the effect of mass of MgH hydride on the driving force for desorption at 275°C at atmospheric pressure... Fig. 1.33 Schematic plot showing the effect of mass of MgH hydride on the driving force for desorption at 275°C at atmospheric pressure...
From the discussion presented above, it is clear that the stability of the debond process can be evaluated by a single parameter, Zmax, which is the shortest (remaining) bond length needed to maintain the debond process stable, and is a constant for a given composite system. Therefore, three different interface debond processes are identified in the following totally unstable, partially stable and totally stable debond processes. The schematic plots of the applied stress versus displacement curves are illustrated in Fig. 4.25 for these debond processes. [Pg.136]

Fig. 22 A schematic plot of the mean square root displacement /(U) of a charge carrier as a function of time for mobilities of... Fig. 22 A schematic plot of the mean square root displacement /(U) of a charge carrier as a function of time for mobilities of...
Figure 11.20 Schematic plot of the overall rate of reaction catalyzed by a surface-bound biocatalyst against the bulk substrate concentration. Figure 11.20 Schematic plot of the overall rate of reaction catalyzed by a surface-bound biocatalyst against the bulk substrate concentration.

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See also in sourсe #XX -- [ Pg.243 , Pg.244 ]

See also in sourсe #XX -- [ Pg.243 , Pg.244 ]




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