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N-Values, determination

From the increased solubility of 2,4-dinitrochlorobenzene in sodium dodecyl sulfate solutions (without NaOH), the authors of this research estimate a K/n of 44. Criticize or defend the following proposition The presence of OH could change the n value for sodium dodecyl sulfate micelles, so exact agreement between K/n values determined by the two methods is not necessarily expected. [Pg.402]

Table 133 Relative Nucleo-philicities of Some Important Environmental Nucleophiles n- Values Determined from the Reaction with Methyl Bromide or n-Hexyl Bromide in Water (Eq. 13-3, s = 1)... Table 133 Relative Nucleo-philicities of Some Important Environmental Nucleophiles n- Values Determined from the Reaction with Methyl Bromide or n-Hexyl Bromide in Water (Eq. 13-3, s = 1)...
Table VI gives intrinsic viscosities of PVC in a series of dialkyl phthalates (34). These results lead to the same conclusions as the n value determinations of Doty and Zable illustrated in Figure 8. Table VI gives intrinsic viscosities of PVC in a series of dialkyl phthalates (34). These results lead to the same conclusions as the n value determinations of Doty and Zable illustrated in Figure 8.
The number of electrons transferred per mole of adrenodoxin (n-value), determined from the slope of the potentiometric titration curve, is 2. This result is further supported by anaerobic titration of the protein with NADPH in the presence of adrenodoxin reductase (30). The result shows that one mole of NADPH is required to reduce one mole of adrenodoxin. Therefore, it is concluded that adrenodoxin transfers two electrons per mole of the protein. Obviously, this conclusion is incompatible with the EPR data which favor the interpretation that one of the two irons is reduced. This discrepancy can not presently be understood in detail. [Pg.24]

Equation (16) was then employed to construct a calibration curve for calculating impurity level by using physical mixtures of SX-II with SX-I in the appropriate composition range (0-14% w/w in this case) (Figure 18). Since the n values determined for all form I samples (GSX, MSX, and SX-I) and physical mixtures were close to 2, the k values for all SX materials were recomputed by iterative curve fitting with the n parameter fixed at 2. The results are presented in Table 4. The refitted k values at = 2 were subsequently used to compute the coefficients C and C2, in Eq. (16). Based on their respective k values and = 2, GSX and MSX were found to contain 0.16 and 0.62% w/ w of metastable nuclei within their crystal matrices. [Pg.322]

EXTRAPOLATED FROM LOWEST S/N VALUE. DETERMINED AFTER CDC COLLABORATIVE STYDY. [Pg.237]

If the charge transfer reaction is the rate-determining step, the equations introduced earlier will describe the current-potential relationship however, the charge number of the electrode reaction will differ from the n value determined, because the latter is characteristic of the rate-determining step. [Pg.54]

In our experimental conditions, the obtained results show a linear variation of V versus In P02, which verify the approximations supposed above. The n values determined from the plot of V versus In P02 show that the (f is the dominant species ( = 4), within the 375-450°C temperature range. [Pg.337]

Figure 4.8 Anodic RDE voitammograms obtained for Cu(ii)-giycine soiutions at 300rpm and different giycine concentrations as indicated, inset contains / n values determined at ri = 0.2 V and plotted versus overequivalent ligand concentration. Figure 4.8 Anodic RDE voitammograms obtained for Cu(ii)-giycine soiutions at 300rpm and different giycine concentrations as indicated, inset contains / n values determined at ri = 0.2 V and plotted versus overequivalent ligand concentration.
The (x, i )), values in Eq. (13-37) are minimum-reflux values, i.e., the overhead concentration that would be produced by the column operating at the minimum reflux with an infinite number of stages. When the light key and the heavy key are adjacent in relative volatihty and the specified spht between them is sharp or the relative volatilities of the other components are not close to those of the two keys, only the two keys will distribute at minimum reflux and the Xi D),n values are easily determined. This is often the case and is the only one considered here. Other cases in which some or all of the nonkey components distribute between distillate and bottom products are discussed in detail by Henley and Seader (op. cit.). [Pg.1274]

Note that if Bn is zero, then T13 and T23 are also zero, so Equation (5.81) reduces to the specially orthotropic plate solution. Equation (5.65), if D11 =D22- Because Tn, T12, and T22 are functions of both m and n, no simple conclusion can be drawn about the value of n at buckling as could be done for specially orthotropic laminated plates where n was determined to be one. Instead, Equation (5.81) is a complicated function of both m and n. At this point, recall the discussion in Section 3.5.3 about the difference between finding a minimum of a function of discrete variables versus a function of continuous variables. We have already seen that plates buckle with a small number of buckles. Consequently, the lowest buckling load must be found in Equation (5.81) by a searching procedure due to Jones involving integer values of m and n [5-20] and not by equating to zero the first partial derivatives of N with respect to m and n. [Pg.308]

The chromatogram of the test sample for plate number determination normally is not a Gaussian-shaped peak, which means that all three equations result in different N values. Therefore, it is important to specify which method is used for the calculation of plate number. If the method used deviates from the normal practice, it must be justified. This is especially true for a column manufacturer. [Pg.433]

Molecular weight determinations have been carried out with methyl-ethyl-, diethyl-, di-n-propyl-, pentamethylene-, and methylphenyl-diazirine. They gave monomeric molecular weights. The three last-named compounds gave the calculated C, H, and N values by the usual procedure of microanalysis. [Pg.125]

For a polytropic process the change of state does not take place at constant entropy, hut for an adiabatic process, it does. Heat may he added to or rejected from a gas in a polytropic process. For a polytropic process, the correlating exponent for the PiVi" component is the exponent n, which becomes an important part of the compressor design, n values are determined from performance testing. [Pg.390]

These methods of test require a knowledge of what is known as the number of degrees of freedom. In statistical terms this is the number of independent values necessary to determine the statistical quantity. Thus a sample of n values has n degrees of freedom, whilst the sum (x — x)2 is considered to have n — 1 degrees of freedom, as for any defined value of x only n — 1 values can be freely assigned, the nth being automatically defined from the other values. [Pg.139]

In the Nernst equation the term RT/nF involves known constants, and introducing the factor for converting natural logarithms to logarithms to base 10, the term has a value at a temperature of 25 °C of 0.0591 V when n is equal to 1. Hence, for an ion M+, a ten-fold change in ionic activity will alter the electrode potential by about 60 millivolts, whilst for an ion M2 +, a similar change in activity will alter the electrode potential by approximately 30 millivolts, and it follows that to achieve an accuracy of 1 per cent in the value determined for the ionic concentration by direct potentiometry, the electrode potential must be capable of measurement to within 0.26 mV for the ion M+, and to within 0.13 mV for the ion M2 +. ... [Pg.549]

Engel et al.92) have estimated the nucleation parameter for H(Pro-Pro-Gly) OH by computing AG° and AS° with Eq. (5) and reported melting temperatures Tm and AH0 values determined calorimetrically. Utilizing the chain length dependence, they obtained the following parameters (in diluted acetic acid at 25 °C n = 5, 10, 14.15) ... [Pg.190]

The exponent n = j3 + X, where j3 is the number of steps involved in nucleus formation (frequently j3 = 1 or 0, the latter corresponding to instantaneous nucleation) and X is the number of dimensions in which the nuclei grow (X = 3 for spheres or hemispheres, 2 for discs or cylinders and 1 for linear development). Most frequently, it is found that 2 < n < 4. Since n is a compound term, the value determined does not necessarily provide a unique measurement of both j3 and X. Ambiguity may arise where, for example, n = 3 could be a consequence of (j3 = 2, X = 1), (j3 = 1,... [Pg.57]

Finally, Katritzky et al.sii have measured first-order rate coefficients for deuteration of pyrimidines by deuterated sulphuric acid (Table 152), and all pD and —D0 values given in the Table refer, as in the earlier work, to a temperature of 20 °C. For 2-aminopyrimidine, reaction clearly occurs on the free base and comparison of the data with the earlier work on anilines and by making a number of assumptions, conjugate acid at higher acidities is apparent and this follows the previously established pattern. This work yielded a value of 0.55 for [Pg.236]

STRATEGY First, write the balanced equation for the cell reaction and the corresponding expression for Q, and note the value of n. Then determine E° from the standard potentials in Table 12.1 or Appendix 2B. Determine the value of Q for the stated conditions. Calculate the emf by substituting these values into the Nernst equation, Eq. 6. At 25.00°C, RT/1 = 0.025 693 V. [Pg.627]

A smaller number of individuals, 132 samples, was analyzed for stable isotopes of nitrogen. There were two objectives to the nitrogen isotope analysis 1) to determine the amount of animal protein in the diet and to look for variation between the sexes and 2) to determine when infants were weaned from the breast. These objectives were addressed by selecting at least ten individuals, when available, from a number of age classes. Figure 1.1 illustrates the age distribution of the sample. Table 1.3 shows the results of these analyses. Individual 5 N values are provided in Herring et al. (1998). [Pg.8]

C and 5 N values were determined by mass spectrometry (MM 903, VG Isogas), equipped with a CN elemental analyzer (Roboprep CN, Europa Scientific). As control for sample purity, C N ratios from the elemental analyser were compared with C N ratios as calculated from the amino acid profile of the same sample. [Pg.177]


See other pages where N-Values, determination is mentioned: [Pg.311]    [Pg.51]    [Pg.265]    [Pg.123]    [Pg.312]    [Pg.386]    [Pg.35]    [Pg.20]    [Pg.508]    [Pg.285]    [Pg.109]    [Pg.204]    [Pg.123]    [Pg.311]    [Pg.51]    [Pg.265]    [Pg.123]    [Pg.312]    [Pg.386]    [Pg.35]    [Pg.20]    [Pg.508]    [Pg.285]    [Pg.109]    [Pg.204]    [Pg.123]    [Pg.94]    [Pg.324]    [Pg.482]    [Pg.22]    [Pg.82]    [Pg.104]    [Pg.25]    [Pg.178]    [Pg.42]    [Pg.389]    [Pg.676]    [Pg.16]    [Pg.45]    [Pg.218]   
See also in sourсe #XX -- [ Pg.187 , Pg.280 ]




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N* values

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