Distributions comparison

Pore size distribution—comparison of results by mercury porosimetry and by adsorption of nitrogen... 

Figure 1 Liquid Residence time distribution comparison - Experimental vs Numerical (a) counter-current operation Liquid flowrate l.SLmm (b) counter-current operation Liquid flowrate 3Lmin (c) co-current operation Liquid flowrate 1.5Lmm (d) co-current operation Liquid flowrate 3Lmm ...

Figure 2 Gas Residence time distribution comparison - Experimental vs Numerical (a) counter-current operation (b) co-current operation.

Robson, A. G. et al. (2003). Macular pigment density and distribution Comparison of fundus autofluorescence with minimum motion photometry. Vision Research 43(16) 1765-1775. 

This abbreviated equation can be used for pore size distribution comparisons of similar samples when absolute pore size is not necessary. If, however, comparison of absolute pore sizes is required, the contact angles should be measured for all samples [42]. 

Blood level may be used to derive kinetic parameters such as half-life, elimination rate constant, AUC, and volume of distribution. Comparison of blood levels after oral and iv may be used to calculate bioavailability. Half-life can be used to predict the effect of repeated dosing. 

The anion-radical of 1,T-binaphthyl acts as the single 77-system with homogeneous spin distribution. Comparison between 1,1 -binaphthyl and biperylenyl in Scheme 3-9 shows their structural similarity. 

Figure 11.6. Oral bioavailability distribution comparison betw/een GPSVS quadrants and Ro5 violations for 613 drugs. Color codes correspond to RankSOral (inset and Table 11.2). See text for details.

Fig. 12. Vertical profile of air distribution. Comparison of experimental results for air-wheat with Eq. (37). H only in the case of the 6-in. column data.

The model assumes that drop coalescence is followed by immediate redispersion into two drops sized according to a uniform distribution. By assuming that the coalescence frequency is independent of drop size, the solution of the resulting form of Eq. (107) is exponential for the equilibrium drop volume distribution. Comparison of the distribution to experimental data is favorable. The analysis is useful in that a functional form for the distribution is obtained. The attendant simplifications necessary for solution, however, do not permit more rational forms of the interaction frequency of droplet pairs in order to account for the physical processes which lead to droplet coalescence and breakage as discussed in Section III. A similar work was presented by Inone et al. (II). 

Many addition polymerization reactions with very low concentrations of impurities have propagation rates much faster than initiation rates and have essentially no termination. Such reactions produce narrow molar mass distributions that can be approximated by the Poisson distribution. Comparison of the polydispersity index of anionically polymerized butadiene with Eq. (1.69) is shown in Fig. 1.20. 

Concerning the potential distribution, comparisons of the Mott-Schottky curves and the flatband potentials as obtained with n- and p-type electrodes of the same semiconductor are of special interest. One example is GaP which has a relatively large bandgap (2,3 eV), The Mott-Schottky plots of the n- and p-type electrodes are given in Fig. 5.18 [32], Since their slopes agree very well with those predicted upon the doping of the... 

Wilbur D S, Vessella R L, Stray J E, et al. (1993). Preparation and evaluation of para-[ At]astatobenzoyl labeled anti-renal cell carcinoma antibody A6H F(ab )2. In vivo distribution comparison with para-[ I]iodobenzoyl labeled A6H F(ab )2. Nucl. Med. Biol. 20 917-927. 

Granted that rate constant data have seldom been unfolded to give the excitation function, to what kind of situation can such rate constants, i.e., k(VfX be applied Rigorously, the answer is none, except in the situation of a mass-spectrometer ion source, since this particular rate constant relates to a very odd effective velocity distribution. Comparison with Eq. (2) shows that the analytical form of this normalized velocity distribution is the following ... 

Pressure and Velocity Field (Varying the Flow Distribution] - Comparison between FBR and PBMR... 

Paul Weisz of Mobil Oil, in a CHEMTECH article (87), showed a product distribution comparison between a zeolite catalyst and an amorphous silica-alumina catalyst, making clear the dramatic difference between them ... 

Figure 7. BFS distribution Comparison between FE analysis and FBG measurements for 7.0 mm crack length.

The only reasonable solution to the size quandary is to use the same measuring technique and measured quantity for comparisons of particle sizes and particle size distributions. Comparisons between instruments that use different measuring procedures are sometimes made but are generally considered to be qualitative. 

Particle Size Distribution Comparisons Between the Nano-DMA (Open) and the Long-DMA (Solid) for Four Different Si02 Aerosol Nanoparticle Distributions. 

Distribution Comparison of costs and service levels between alternatives... 

Velocity distribution comparison in cross-sections 0-Aand 0-5(Figure 12.1) according to the simplified analytical model shows that the simpli-... 

Co-ordinated Nitrenes.— The complex rm -[RuCl(Ng)(diars)2] reacts in hydrochloric acid to produce approximately equal numbers of molecules of [RuCl(NH3)(diars)g]+ and [RuCl(N2)(diars)a]+. When this reaction is carried out with N-labelled complex containing specifically Ru( N N N), the dinitrogen complex produced contains exclusively Ru( N N). This result is consistent with a co-ordinated nitrene (Ru N) intermediate, similar to those previously reported for reactions of ruthenium(m)-azide complexes. However, product and product-distribution comparisons between the ruthenium(ii)-and ruthenium(m)-azide plus hydrochloric acid reactions suggest that there must be some difference in mechanism between the complexes of the two different oxidation states. It is therefore proposed that for the rra j-[RuCl(N3> (diars)a] reaction the first step is protonation of the co-ordinated azide, which may occur at either end, followed by a split into Ng plus NH, which gives an ammonia ligand one way and a dinitrogen ligand the other ... 

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