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Values reproducible

Pressure and volume values converted, and entPalpy and entropy values reproduced, from Hust and Stewart, NBS TecP. Note 202, 1963. TPis source gives values at and above 72.373 K at closer pressure intervals, c = critical point. Tbe notation 1.268.-3 signifies 1.268 x 10" ... [Pg.269]

Values reproduced or converted from Goodwin, Roder, and Straty NBS Tecb. Note 684, 1976. t = triple point c = critical point. Tbe notation 1.131.—5 signifies 1.131 X 10" ... [Pg.277]

Values reproduced or converted from a tabulation by Tsykalo and Tabacbnikov in V A. Rabinovich (ed.), Theimophysical Propeities of Gases and Liquids, Stan-dartov, Moscow, 1968 NBS-NSF transl. TT 69-55091, 1970. Tbe reader may be reminded that very pure hydrogen peroxide is very difficult to obtain owing to its decomposition or instability, c = critical point. Tbe FMC Corp., Philadelphia, PA tech. bull. 67, 1969 (100 pp.) contains an enthalpy-pressure diagram to 3000 psia, 1100 K. [Pg.290]

The K constant is usually taken as 1.75 this value reproduces the rotational barrier in ethane. [Pg.93]

Furthermore, the electrical conductivities of liquid Na-Sn alloys for the five compositions are determined with the Kubo-Greenwood scheme, using the trajectories from our ab initio MD simulations. The calculated values reproduce the measured strong variation of the conductivity with the Na (or Sn) concentration very well. The small (semimetallic) conductivity of the alloys with nearly equimolar composition can be explained by the position of the Fermi energy between the occupied sp-band of tin and the sp-band of sodium. [Pg.281]

Fig. 10. Comparison of the measured refractive indices for PET film with values calculated from the orientation functions determined from n.m.r. assuming transversely isotropic structural units. I, Experimental points predicted values. Reproduced from Polymer by permission of the publishers, Butterworth Co (Publishers) Ltd. (C)... Fig. 10. Comparison of the measured refractive indices for PET film with values calculated from the orientation functions determined from n.m.r. assuming transversely isotropic structural units. I, Experimental points predicted values. Reproduced from Polymer by permission of the publishers, Butterworth Co (Publishers) Ltd. (C)...
Fig. 13. Frequency dependences of the complex viscosity, q, for melts of linear and branched PMM A with different M values. (Reproduced with permission from [88]. Copyright 2001 American Chemical Society.)... Fig. 13. Frequency dependences of the complex viscosity, q, for melts of linear and branched PMM A with different M values. (Reproduced with permission from [88]. Copyright 2001 American Chemical Society.)...
Figure 1.3 Relative decline in resources consumed to create a unit of economic value. Reproduced from... Figure 1.3 Relative decline in resources consumed to create a unit of economic value. Reproduced from...
Figure 2. Relation between the intrinsic viscosity and the number-averaged molecular weight of trimethylsilylated alkoxide polymeric particles for Si(0C2H5) solutions with different r values. (Reproduced with permission from Ref. 3. Copyright 1984 North Holland Physics Publishing.)... Figure 2. Relation between the intrinsic viscosity and the number-averaged molecular weight of trimethylsilylated alkoxide polymeric particles for Si(0C2H5) solutions with different r values. (Reproduced with permission from Ref. 3. Copyright 1984 North Holland Physics Publishing.)...
Fig. 6. Difference spectra between xanthine oxidase inactivated with various pyra-zolo [3, 4-d] pyrimidines and the native enzyme. The spectra are believed to represent the increase in absorption occurring when Mo(VI) of native enzyme is converted to Mo(IV) complexed with the inhibitors. Spectra were obtained by treating the enzyme with inhibitors in the presence of xanthine, then admitting air, so as to re-oxidize the iron and flavin chromophores. The extinction coefficients, de, are expressed per mole of enzyme flavin. Since some inactivated enzyme was present, extinction coefficients per atom of molybdenum of active enzyme will be about 30% higher than these values. (Reproduced from Ref. 33, with the permission of Dr. V. Massey.)... Fig. 6. Difference spectra between xanthine oxidase inactivated with various pyra-zolo [3, 4-d] pyrimidines and the native enzyme. The spectra are believed to represent the increase in absorption occurring when Mo(VI) of native enzyme is converted to Mo(IV) complexed with the inhibitors. Spectra were obtained by treating the enzyme with inhibitors in the presence of xanthine, then admitting air, so as to re-oxidize the iron and flavin chromophores. The extinction coefficients, de, are expressed per mole of enzyme flavin. Since some inactivated enzyme was present, extinction coefficients per atom of molybdenum of active enzyme will be about 30% higher than these values. (Reproduced from Ref. 33, with the permission of Dr. V. Massey.)...
Fig. 17 Comparison of the electron acceptor properties of JV-nitropyridinium cations (XPyNO ) as measured by their E% values in relationship to the thermodynamic acidities of the corresponding hydropyridinium cations (XPyH+) as evaluated by their pXa values. Reproduced with permission from Ref. 235a. Fig. 17 Comparison of the electron acceptor properties of JV-nitropyridinium cations (XPyNO ) as measured by their E% values in relationship to the thermodynamic acidities of the corresponding hydropyridinium cations (XPyH+) as evaluated by their pXa values. Reproduced with permission from Ref. 235a.
Figure 1.6 Solvent accessibility and photobleaching behaviour of nanoparticle synthesis intermediates. (A-C) Excitation and emission spectra of nanoparticle intermediates ((A) TRITC (B) core (C) core-shell) in ethanol (blue) and water (red). (D) Photobleaching behaviour of nanoparticle intermediates (blue, TRITC green, core red, core-shell) and fluorescein (black). All curves in (A)-(D) are normalized by the peak values. (Reproduced from ref. 13, with permission.)... Figure 1.6 Solvent accessibility and photobleaching behaviour of nanoparticle synthesis intermediates. (A-C) Excitation and emission spectra of nanoparticle intermediates ((A) TRITC (B) core (C) core-shell) in ethanol (blue) and water (red). (D) Photobleaching behaviour of nanoparticle intermediates (blue, TRITC green, core red, core-shell) and fluorescein (black). All curves in (A)-(D) are normalized by the peak values. (Reproduced from ref. 13, with permission.)...
Figure 2. Redox potentials for formation of 9 and 10 vs the sum ofNICS values (Reproduced from reference 7. Copyright 2005 American Chemical Society.)... [Pg.235]

Figure 4. Equilibrium adsorption densities of polyacrylic acid on hematite at various pH values. Reproduced with permission from Ref. 22. Copyright 1983, Colloids and Surfaces. Figure 4. Equilibrium adsorption densities of polyacrylic acid on hematite at various pH values. Reproduced with permission from Ref. 22. Copyright 1983, Colloids and Surfaces.
Fig. 22 Wet thickness at pH = 5.8 for PAA (Mn = 4.8 kDa) as a function of the grafting density and ionic strength of the aqueous solution in the a OB regime and b the SB regime. The symbols represent different IS values. (Reproduced with permission from [89])... Fig. 22 Wet thickness at pH = 5.8 for PAA (Mn = 4.8 kDa) as a function of the grafting density and ionic strength of the aqueous solution in the a OB regime and b the SB regime. The symbols represent different IS values. (Reproduced with permission from [89])...
From the anisotropic contributions to the HFCs, it is confirmed that the reduced site is the main source of anisotropy in the system. The computed values reproduce the rhombicity of all anisotropic hyperfine tensors, but there is a clear tendency of overestimation. In any case, since the anisotropic components are at least an order of magnitude smaller than the isotropic contributions to the HFC, it is more appropriate and useful to focus on the latter. All isotropic HFCs have the correct signs with respect to the... [Pg.341]

FIGURE 2.3 Caffeine solubility in dioxane-water binary solvents. The curve is an interpolation between calculated values. (Reproduced from Adjei, A., J. Newburger, andA. Martin. D9P i.arm. Sci69 659-661. Copyright 1980, American Pharmacists Association. Reprinted with permission from Wiley-Liss, Inc., a subsidiary of John Wiley Sons, Inc.)... [Pg.15]

FIGURE 2.4 Extended Hansen Solubility Approach applied to the solubility oftemazepam in solvents covering a wide range of polarities. The line represents equal calculated and experimental values. (Reproduced from Richardson, P. J., D. F. McCafferty, and A. D. V foolfson. 1992. J. Pharm.78 189-198. Copyright Elsevier 1992. With permission from Elsevier Science B.V.)... [Pg.17]

Figure 2.19 Oxygen saturation curves for myoglobin and haemoglobin and different pH values. (Reproduced by permission of John Wiley Sons, Ltd). Figure 2.19 Oxygen saturation curves for myoglobin and haemoglobin and different pH values. (Reproduced by permission of John Wiley Sons, Ltd).
Table 4.7 Examples of calculated MR values. Reproduced by permission of John Wiley and Sons Ltd. from Hansch C. and Leo A.J. Substituents Constants for Correlation Analysis in Chemistry and Biology (1979)... Table 4.7 Examples of calculated MR values. Reproduced by permission of John Wiley and Sons Ltd. from Hansch C. and Leo A.J. Substituents Constants for Correlation Analysis in Chemistry and Biology (1979)...
Source Complied by Varian Associates. Absolute values. Reproduced with permission. [Pg.199]

FIGURE 10.16 XRD of PA6, clay, PA6/clay (5%), and carbonaceous floccules collected at various fractions of sample mass loss at 50kW/m2 in N2. PA6 and PA6/clay original values reduced to 10% of measured values. (Reproduced from Kashiwagi, T. et al., Polymer, 45, 881, 2004. With permission.)... [Pg.255]

Fig. 19. Profiles of the 23Na concentration in OPC samples with w/c ratios of 0.3, 0.4 and 0.5 soaked in brine, showing enhanced uptake for larger w/c values. (Reproduced from Ref. 98 with permission from Elsevier.)... Fig. 19. Profiles of the 23Na concentration in OPC samples with w/c ratios of 0.3, 0.4 and 0.5 soaked in brine, showing enhanced uptake for larger w/c values. (Reproduced from Ref. 98 with permission from Elsevier.)...
FIGURE 43. Calculated geometries at MP2 and relative energies at MP4 of the stationary points of the reaction path for the addition of ( Ai) EF2 to ethylene. Precursor complexes Comp-EF2, transition states TS-EF2 and products Pro-EF2. Bond distances are in A, bond angles in deg. The energy values are AH° values and they are in kcalmoU. The numbers in parentheses give the A//298 values. Reproduced by permission of John Wiley Sons, Inc. from Reference 87... [Pg.276]

FIGURE 1. Representative cyclic voltammogram of a 2,2-dimesityl enol in which the two electron removals involved in the ECE determining steps proceed at the same potential value . Reproduced from Reference 134 by permission of Wiley-VCH... [Pg.491]


See other pages where Values reproducible is mentioned: [Pg.313]    [Pg.316]    [Pg.329]    [Pg.330]    [Pg.338]    [Pg.341]    [Pg.341]    [Pg.342]    [Pg.92]    [Pg.170]    [Pg.370]    [Pg.238]    [Pg.35]    [Pg.403]    [Pg.669]    [Pg.438]    [Pg.172]    [Pg.234]    [Pg.952]    [Pg.128]    [Pg.284]   
See also in sourсe #XX -- [ Pg.127 ]




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Reproducibility

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