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Three-dimensional presentation

Figure 2.14. Cross-sectional view of a NaCl ionic crystal one Na above and one Na below the central CP ion, for a three-dimensional presentation. Figure 2.14. Cross-sectional view of a NaCl ionic crystal one Na above and one Na below the central CP ion, for a three-dimensional presentation.
Figure 4. Hexagonal superstructures of AB and AB3 alloys (B19, B81 DOi9, and other structures) in three-dimensional presentation and in projection on the equatorial plane. The sites of elementary cell are indicated by dotted lines... Figure 4. Hexagonal superstructures of AB and AB3 alloys (B19, B81 DOi9, and other structures) in three-dimensional presentation and in projection on the equatorial plane. The sites of elementary cell are indicated by dotted lines...
Three dimensional presentations are cumbersome and it is more convenient to transform the Hansen parameters into fractional parameters as defined by [14]... [Pg.459]

Biochemists continue to be the main exploiters of photophysical techniques,though it should be pointed out that the coverage of these particular aspects is selective rather than comprehensive. Even processes in living cells are now b ing studied (Vigo et al.. inter alia). Some aspects of biological photochemistry are undoubtedly an acquired taste. For example, a three-dimensional presentation of the total fluorescence from urine has enabled Leiner et al. to identify several fluorescent metabolites. [Pg.551]

Figure 27. Lower, three-dimensional presentation of the spectral region, 0.5-6.0 ppm of a 360 MHz spin-echo-correlated H-NMR spectrum of BPTI. The chemical shift, 5, on the horizontal axis corresponds to that in conventional, one-dimensional spectra. Ad on the vertical axis stands for the difference frequencies between correlated nuclei. Cross-peaks between J-coupled nuclei are at 0.5 Ad. The solvent singlet resonance is at 4.35 ppm. Upper, contour plot of the same spin-echo-correlated spectrum of the inhibitor. Figure 27. Lower, three-dimensional presentation of the spectral region, 0.5-6.0 ppm of a 360 MHz spin-echo-correlated H-NMR spectrum of BPTI. The chemical shift, 5, on the horizontal axis corresponds to that in conventional, one-dimensional spectra. Ad on the vertical axis stands for the difference frequencies between correlated nuclei. Cross-peaks between J-coupled nuclei are at 0.5 Ad. The solvent singlet resonance is at 4.35 ppm. Upper, contour plot of the same spin-echo-correlated spectrum of the inhibitor.
Figure 6.41 Schematic three-dimensional presentation of the geometries of cyclodextrins. Figure 6.41 Schematic three-dimensional presentation of the geometries of cyclodextrins.
There are several steps of calculation involved in arriving at the three-dimensional presentation. They are necessary in order to reduce the number of variables from four to three. The first step in obtaining the curves in Figure 6 is to recalculate... [Pg.159]

In Fig. 6.2, a more general three-dimensional presentation of the penetration of a projectile into a solid is shown. In this schematic, an energetic projectile enters the sample surface at the point (0, 0,0), at a angle a to the surface normal. The projectile is stopped at the point (x, z ). For this presentation of an ion s pene-... [Pg.64]

Raw data have to be presented in some chosen form. Some of the data is collected as a function of time, some as a function of frequency. If data are collected as a function of both frequency and time, the need for a three-dimensional presentation is present. [Pg.370]

Figure 5.14 Three-dimensional presentation of molecular mass distribution and chemical composition distribution for a poly(styrene-methyl methacrylate) block copolymer [72]. Figure 5.14 Three-dimensional presentation of molecular mass distribution and chemical composition distribution for a poly(styrene-methyl methacrylate) block copolymer [72].
A quasi-three-dimensional presentation of the potential energy surface of a fissioning nucleus as a function of deformation and asymmetry is shown in Fig. 4.9. [Pg.242]

A three-dimensional presentation of the identification of the parameters is given in Figure 15.11 for the rate parameter of the main reaction and the final activity, while Figure 15.12 displays this for the main reaction and the coking rate parameters. These outcomes provide an overview of the difficulty of the parameter optimization task. [Pg.371]

Figure 6a Glass transition temperatures of tyrosine-derived polyarylates. In this three dimensional presentation, the pendent chain length is plotted on the y axis, the length of the diacid component in the polymer backbone is plotted on the x axis, and the measured glass transition temperatures are plotted on the z axis. Figure 6a Glass transition temperatures of tyrosine-derived polyarylates. In this three dimensional presentation, the pendent chain length is plotted on the y axis, the length of the diacid component in the polymer backbone is plotted on the x axis, and the measured glass transition temperatures are plotted on the z axis.
Fig. 3.1 Three-dimensional presentation of dual agonist 2 bound in the ligand binding pocket of human PPARy (reproduced from [5], with the permission of Elsevier Inc.)... Fig. 3.1 Three-dimensional presentation of dual agonist 2 bound in the ligand binding pocket of human PPARy (reproduced from [5], with the permission of Elsevier Inc.)...
Fig. 2.6.2. Three-dimensional presentation of the same tumor volume CE-CT (purple), Tj-weighted MRT without enhancement (blue)... Fig. 2.6.2. Three-dimensional presentation of the same tumor volume CE-CT (purple), Tj-weighted MRT without enhancement (blue)...
Figure 6.54 Three-dimensional presentation of transmission radiographs for a detonation propagating up a 7.f degree PBX-9502 cone. Times are from load ring or when detonator was initiated. Figure 6.54 Three-dimensional presentation of transmission radiographs for a detonation propagating up a 7.f degree PBX-9502 cone. Times are from load ring or when detonator was initiated.
FIGURE 20 Three-dimensional presentation of the geometries of cyclodextrin. [From Braithwaite, A., and Smith, R J. (1996). Chromatographic Methods, 5th Ed. Chapman Hall, London.]... [Pg.225]


See other pages where Three-dimensional presentation is mentioned: [Pg.53]    [Pg.81]    [Pg.225]    [Pg.373]    [Pg.39]    [Pg.329]    [Pg.31]    [Pg.62]    [Pg.64]    [Pg.36]    [Pg.275]    [Pg.50]    [Pg.270]    [Pg.173]    [Pg.1399]    [Pg.194]    [Pg.71]    [Pg.825]    [Pg.128]    [Pg.143]    [Pg.358]    [Pg.235]   
See also in sourсe #XX -- [ Pg.194 , Pg.204 , Pg.229 ]




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