Our previous conclusions

Our previous conclusions will all have some dependence on the particular type of application considered, an aspect which may influence the total CPU work load, the amount of data transfer required, and the possibility of obtaining even load balancing. Our findings in this work would suggest that load balancing does not constitute a problem for Cl applications of reasonable size, and the success or failure of the parallelization will therefore be determined... 

It should perhaps be pointed out that if the diffusion theory were true, our previous conclusions about the relation between the true and apparent order of the reaction would have to be modified. In general the reaction rate would depend upon the first power of the concentration of... 

Even with the use of the PCM method, which allows us to overcome some of the limitations of DFT calculations, our study is necessarily qualitative. Flowever, the preliminary PCM calculations give further support to our previous conclusions on the effect of... 

Let us now consider the particle current in the high-field limit for the cases depicted in Fig. 13. Equation (90) is applicable to each of these cases, so that it is possible to examine the predicted effects of the immobile (trapped) space charge on these particle currents. Utilizing our previous conclusion that space charge having the same sign as the surface-charge... 

The P value for the one-sided test is 0.038, in line with our previous conclusion that it produced a significant result. The two-sided test would yield a P value exactly twice as large, i.e. 0.076 (non-significant). 

There is significant evidence confirming our previous conclusion that yield varies according to which catalyst is used (P < 0.001). 

In the series Ba2+, Cu2+, Y3+ the cation size increases. These cations do not create the ion pairs with anion NO3 and the dependence of es on the ion strength for nitrate salts is in agrement with our previous conclusions about the dependence of the solvent dielectric constant on the ion concentration with change of 5. For the formate salts, these cations create ion pairs with anions CHOO- due to hydrogen bonds between anion and water molecules from the hydration shell of cation thus, the degree of association increases with the decrease of ion size. As a result, we obtaine the concentration dependence for es that is opposite to nitrate salts. Since the considered theory is elaborated for the symmetrical electrolytes and experimental data concern the asymmetri-... 

Therefore, the increase in absolute rate constant for the reaction of the hydrated electron with the molecule upon unfolding is either because of an increase in reactivity of the reactive sites or to a better exposure of available reactive sites. There is no evidence for a substantial increase in reactivity of amino acid residues with a change in conformation of the protein. The exposure of reactive sites must be the main reason for the increased reactivity. This confirms our previous conclusions (3). 

The activation of N2O to produce atomic O species is an essential step in the reactions investigated here and is controlled by the presence of extrafi amework iron species. In an earlier work, we demonstrated that extraframework A1 or Ga species, as well as Bronsted sites in the catalysts play a minor role in N2O activation. Taking this into account, the activity differences between FeZSM-5 (873 K) and Fe-silicalite (873 K) in Fig. 2 are strictly related to the distinct nature of the (extraframework) iron species in the catalysts. The similarity between the iron species and activities of FeZSM-5 (873 K) and Fe-silicalite (1173 K) further supports our previous conclusion. 

Thus far we have assumed that the electronic ground state itself is not involved in the vibronic coupling but simply serves as an inert probe for the coupling between excited states. If the ground state is subject to coupling through the mode being probed, complications arise that lead to modification of some of our previous conclusions. 

These results for hie transuranium isotopes tend to confirm our previous conclusions that hie fission-fusion approach to microfission eiqiloslans is the one to be pursued. 

Recent results (see Bontemps et al., this volume) have shown that, contrary to our previous conclusion, the cytoplasmic 5 -nucleotidase operates in hepatocytes in basal conditions and participates in a futile cycle. This activity could be confirmed when a highly purified cytoplasmic 5 -nucleotidase, prepared according to Itoh (1981) was assayed in physiological conditions (see also Fig. 4) instead of the partially purified enzyme we used previously. 

This relatbnship is respected (fig.6 ), and Kj depends on the strain and on the fermentation system. All our previous conclusions are, of course, confirmed by this representation. It does clearly appear that, as the fermentor which has the lowest Z = P/Vl is more worthy of interest, it will of course be more bulky. The compromise between these two contradictory factors which, in the absence of other requirements, will go to make up the criteria for fermentor choice. 

This agrees with our previous conclusion that for positive values of x polymers of average and high molecular weight do not mix at all. 

The shapes of the low and high frequency spectral densities (see also figure 3) can be nicely compared, a result in perfect qualitative agreement with our theoretical predictions. This supports also our previous conclusion that, basically, they take a common origin and must contain information on the same time scale. 

In conclusion, these observations support our previous conclusions (Marini et al, 2010a) that preformed Om (either plasma Om or Om from Arg hydrolyzed locally in the small intestine) is the preferred precursor for the Cit synthesis, rather than tfe novo Om produced from Gin or Pro by action of ornithine aminotransferase. 

Finally, neutron diffraction experiments clearly confirm our previous conclusions drawn from the shape of the adsorption isotherms and from the microcalorimetric studies [16] the step at at about p/p =0.12 on the N2 adsorption isotherms is due to a fluid - solid transition of the adsorbate. Also, as soon as nitrogen is adsorbed, the zeolite structure progressively undergoes a change from monoclinic to orthorhombic structure. 

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