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Activity calculations

In summary, the Energy of Activation calculated from repeated experiments with 5% random error is ... [Pg.113]

The rates of decarboxylation of a range of 3-substituted mesitoic acids in 82.1 wt. % phosphoric and 83.0 wt. % sulphuric acids have been measured636 over a range of temperatures as indicated in Table 209, which gives the first-order rate coefficients together with the log A values and the energies, enthalpies, and entropies of activation calculated at 80 °C for sulphuric acid, and 119 °C for phosphoric acid these kinetic parameters are somewhat different from those... [Pg.306]

Figure 3. Time series of nitrate (Slagle and Heimerdinger 1991) and dissolved, particulate, and total in surface water at 47°N, 20°W (Atlantic Ocean) in April-May 1989. activity calculated as 0.0686 salinity (Chen et al. 1986). The production of biogenic particles during the bloom enhances the scavenging of Th, resulting in growing disequilibrium with time due to sinking of particles. Figure 3. Time series of nitrate (Slagle and Heimerdinger 1991) and dissolved, particulate, and total in surface water at 47°N, 20°W (Atlantic Ocean) in April-May 1989. activity calculated as 0.0686 salinity (Chen et al. 1986). The production of biogenic particles during the bloom enhances the scavenging of Th, resulting in growing disequilibrium with time due to sinking of particles.
From the data listed in Table 6 the van der Waals volume of the Diels-Alder reac-tion13,25,52,65 can be calculated to be with AVw = — 11.2 cm3 mol 1 only roughly one-quarter of the experimentally accessible volume of reaction (AV = —41.7 cm3 mol-1) (Scheme 3). Consequently, a significant part of the observed A V results from the higher packing of the cyclic product (compared to the acyclic reactants) rather than from the changes in bonding. The difference between the van der Waals volume of activation calculated for the pericyclic and stepwise reaction is small (5AV y = —1.7 cm3 mol-1) and is inconsistent with the experimental data listed in Tables 4 and 5. In order to explain... [Pg.561]

SCHEME 3. Comparison of van der Waals volumes of reaction and activation with the volumes of reaction and activation calculated for a pericyclic and stepwise Diels-Alder reaction of 1,3-butadiene with ethene... [Pg.564]

SCHEME 18. van der Waals volume of activation AV and volume of activation calculated for degenerate Cope rearrangement of 1,5-hexadiene... [Pg.597]

The program produces in its output dataset a block of results that shows the concentration, activity coefficient, and activity calculated for each aqueous species (Table 6.4), the saturation state of each mineral that can be formed from the basis, the fugacity of each such gas, and the system s bulk composition. The extent of the system is 1 kg of solvent water and the solutes dissolved in it the solution mass is 1.0364 kg. [Pg.84]

Where only univalent cations are considered, the activities calculated by Equations 9.27 and 9.28 are equivalent in value, but this is not the case if divalent ions are included. The reaction describing exchange of sodium for calcium ions,... [Pg.144]

Since >X 2Ca++ has a double charge, and because the CEC and TEC in this case differ in value, the activities calculated for the species according to the two conventions differ. [Pg.144]

H6(Me3Si)C7B-Me]Ti(H5C5B-Me) Theoretical studies Catalytic activity calculations S, X, H, B, C, IR 144... [Pg.33]

The activity calculated from (7) comprises both film and pore diffusion resistance, but also the positive effect of increased temperature of the catalyst particle due to the exothermic reaction. From the observed reaction rates and mass- and heat transfer coefficients, it is found that the effect of external transport restrictions on the reaction rate is less than 5% in both laboratory and industrial plants. Thus, Table 2 shows that smaller catalyst particles are more active due to less diffusion restriction in the porous particle. For the dilute S02 gas, this effect can be analyzed by an approximate model assuming 1st order reversible and isothermal reaction. In this case, the surface effectiveness factor is calculated from... [Pg.333]

In this way and by numerical evaluation, Driessens (2) proved that the experimental activities could be explained on the basis of substitutional disorder, according to Equation (27), within the limits of experimental error. It seems, therefore, that measurements of distribution coefficients and the resulting activities calculated by the method of Kirgintsev and Trushnikova (16) do not distinguish between the regular character of solid solutions and the possibility of substitional disorder. However, the latter can be discerned by X-ray or neutron diffraction or by NMR or magnetic measurements. It can be shown that substitutional disorder always results in negative values of the interaction parameter W due to the fact that... [Pg.534]

So by poor experimental design, we have allowed a liquid junction potential to form in our cell. While we have the same emf as in the first cell, in fact the activity of copper ion in this new cell is only 9.5% of the activity calculated for the case where no liquid junction potential was induced. [Pg.77]

The capsules contained a mean of 82 mg feverfew and thus the level of activity calculated as parthenolide can be estimated as 0.67%. Other studies quote 0.87% sesquiterpene lactones calculated as parthenolide [27] and 0.25-0.30% of active (antimicrobial) material [33]. Bohlmann s extraction of individual components from the dried plant yielded 116 mg sesquiterpene lactones/kg dried feverfew which amounts to less than 0.01 % [17]. Another extraction yielded 330 mg endoperoxides/kg and 56 mg canin/kg alone [19] which would amount to a level of sesquiterpene lactones of at least 0.04%. Thus, the level of sesquiterpene lactones appears to vary with different sources of the plant and this could have been due to a number of factors including the conditions in which feverfew was grown, the season in which it was picked and the way in which it was stored. Another important determinant of the parthenolide content of feverfew appears to be the geographical location. A recent survey of commercial preparations found that all the North American commercial products tested contained less that 0.1% parthenolide, wheras much higher values were obtained for British products. A minimum level of 0.2% parthenolide in commercial products has been proposed by the Health Protection Branch of Health and Welfare Canada [71]. [Pg.235]

When using standard solutions prepared on the basis of activities calculated from these activity scales, and provided there is no interfierence and that the prelogarithmic term in the E versus log a dependence is Nernstian or at least accurately known and constant, the sample activity can be determined from the ISE potentials obtained in the sample and in a standard solution (see (4.13), p. 74-6). [Pg.101]

Sihcon can be used to make solar cells to provide electricity for light-activated calculators and satellites. It also has the ability to convert sunlight into electricity. [Pg.196]

As the next enzymes of the heme pathway are active, uroporphyrinogen is converted to heptacarboxyporphyrinogen during the enzymatic reaction. This can be overcome if the incubation temperature is raised to 45°C, which inactivates uroporphyrinogen decarboxylase. Yet, 37°C is the standard temperature for enzyme activity determinations. Despite our neglect of the additionally formed porphyrins by uroporphyrinogen decarboxylase in the activity calculations, we found a highly reliable test performance. [Pg.777]

For chemicals in condensed phases (e.g., NOM, lipids), such an activity calculation is sensitive to the system temperature as described by (Eq. 3-51) ... [Pg.357]

For a series of silica-supported metals, the specific activity, calculated as the rate coefficient at 100° C referred to unit area of metal, has been found [155] to decrease in the order Pd > Rh > Pt > Ni > Co > Ru > Ir Fe, Os = 0. For pumice-supported metals, the corresponding... [Pg.76]

Using activities, calculate the pH of a solution containing 0.010 M NaOH plus 0.012 0 M LiN03. What would be the pH if you neglected activities ... [Pg.155]

Including activities, calculate the voltage of the cell Ni(s) NiS04(0.002 0 M) CuC12(0.003 0 M) Cu(.v). Assume that the salts are completely dissociated (that is, neglect ion-pair formation). [Pg.295]

THE ENERGY OF ACTIVATION Ex is the heat of activation calculated from the equation number of effective impacts EjRT total number of impacts —... [Pg.97]

Explain the derivation of Equation El0.4 for malate dehydrogenase activity calculation. [Pg.369]

The final protein content of the solution is 2.8 mg/ml. The solution has 7 U/ml of specific activity, calculated using azocasein as substrate (see Basic Protocol 2, steps 1 to 8). All enzymes are available from Sigma. [Pg.151]

Figure C4.2.2 LOX activity measurements by both oxygen electrode (right) and UV absorbance (left). The graph shows a hypothetical reaction using identical conditions of equal substrate and LOX concentrations and temperature set at 25°C. Over the range generally used for measurement, the UV method gives a 3.24-fold greater response compared to the oxygen electrode that is, the full-scale of oxygen uptake (0 to 100) represents 0.242 pmol 02/ml of solution and the full-scale of UV-absorbance (0 to 2.0) represents 0.0746 pmol product/ml of solution. Also shown is the lag phase followed by a rapid linear rate used for activity calculation. Figure C4.2.2 LOX activity measurements by both oxygen electrode (right) and UV absorbance (left). The graph shows a hypothetical reaction using identical conditions of equal substrate and LOX concentrations and temperature set at 25°C. Over the range generally used for measurement, the UV method gives a 3.24-fold greater response compared to the oxygen electrode that is, the full-scale of oxygen uptake (0 to 100) represents 0.242 pmol 02/ml of solution and the full-scale of UV-absorbance (0 to 2.0) represents 0.0746 pmol product/ml of solution. Also shown is the lag phase followed by a rapid linear rate used for activity calculation.
Tocopherols and tocotrienols AOAC methods, 479-480 (tables) biological activity, calculation of, 489 characteristics and structure of, 485-486 HPLC, 480-481,486-487, 489 sample preparation, 481 -485, 487-489 Tocotrienols. see Tocopherols and tocotrienols... [Pg.767]

Nafion SAC-13 exhibited the highest specific activity calculated by taking into account the number of acidic sites. [Pg.744]

First, it is of common interest to unsteady processes and their models. Chemical unsteadiness must be taken into account in many cases. For example, studies with variations in catalyst activity, calculations of fluidized catalyst bed processes (when the catalyst grain "is shaking in a flow of the reaction mixture and has no time to attain its steady state), analyses of relaxational non-stationary processes and problems of control. Unsteady state technology is currently under development [14,15], i.e. the technology involving programmed variation of the process parameters (temperature, flow rate, concentration). The development of this technology is impossible without distinct interpretation of the unsteady reaction behaviour. [Pg.5]


See other pages where Activity calculations is mentioned: [Pg.422]    [Pg.462]    [Pg.834]    [Pg.292]    [Pg.291]    [Pg.33]    [Pg.118]    [Pg.70]    [Pg.154]    [Pg.154]    [Pg.186]    [Pg.94]    [Pg.422]    [Pg.462]    [Pg.834]    [Pg.10]    [Pg.308]    [Pg.230]   
See also in sourсe #XX -- [ Pg.74 ]

See also in sourсe #XX -- [ Pg.514 ]




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