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Intersection points analysis

Intersection point analysis is much less dependable on the quality of experimental data than the first two criteria, and the Haldanes are reaUy the same for... [Pg.171]

Substrate titration. Imagine that the two straight-line portions of Fig. 6-1 were allowed to intersect. What is the significance of the intersection pH Show that the value of log k, at the intersection point is 0.301 units smaller than log ( W- Conduct a similar analysis of Fig. 6.1 b. [Pg.151]

A direct linear plot made from seven pairs of (v, [S]) data. The dotted lines mark the lowest and highest points of intersection. Clearly, a graph showing 21 horizontal and 21 vertical dotted lines, equivalent to the number of intersections from seven data pairs (see text), would be cluttered and difficult to interpret, and these lines are not shown. Rather, the hatched lines indicate Km and values obtained from nonlinear regression of the same data not surprisingly, these lie close to the median intersection points that would be obtained from a full direct linear analysis... [Pg.107]

Consider the standard Uni Uni mechanism (E + A EX E + P). A noncompetitive inhibitor, I, can bind reversibly to either the free enzyme (E) to form an El complex (having a dissociation constant K s), or to the central complex (EX) to form the EXl ternary complex (having a dissociation constant Xu). Both the slope and vertical intercept of the standard double-reciprocal plot (1/v vx. 1/[A]) are affected by the presence of the inhibitor. If the secondary replots of the slopes and the intercepts (thus, slopes or vertical intercepts vx [I]) are linear (See Nonlinear Inhibition), then the values of those dissociation constants can be obtained from these replots. If Kis = Xu, then a plot of 1/v vx 1/[A] at different constant concentrations of the inhibitor will have a common intersection point on the horizontal axis (if not. See Mixed-Type Inhibition). Note that the above analysis assumes that the inhibitor binds in a rapid equilibrium fashion. If steady-state binding conditions are present, then nonlinearity may occur, depending on the magnitude of the [I] and [A] terms in the rate expression. See also Mixed Type Inhibition... [Pg.507]

Because of the aforementioned EDA hypotheses, the ellipses of different categories present equal eccentricity and axis orientation they only differ for their location in the plane. By coimecting the intersection points of each couple of corresponding ellipses, a straight line is identified which corresponds to the delimiter between the two classes (see Eig. 2.15B). Eor this reason, this technique is called linear discriminant analysis. The directions which maximize the separation between classes are called EDA canonical variables. [Pg.88]

Quadratic discriminant analysis (QDA) is a probabilistic parametric classification technique which represents an evolution of EDA for nonlinear class separations. Also QDA, like EDA, is based on the hypothesis that the probability density distributions are multivariate normal but, in this case, the dispersion is not the same for all of the categories. It follows that the categories differ for the position of their centroid and also for the variance-covariance matrix (different location and dispersion), as it is represented in Fig. 2.16A. Consequently, the ellipses of different categories differ not only for their position in the plane but also for eccentricity and axis orientation (Geisser, 1964). By coimecting the intersection points of each couple of corresponding ellipses (at the same Mahalanobis distance from the respective centroids), a parabolic delimiter is identified (see Fig. 2.16B). The name quadratic discriminant analysis is derived from this feature. [Pg.88]

Another possibility of determining the gel point with the help of rheological methods is dynamical mechanical spectroscopy. Analysis of change of dynamic mechanical properties of reactive systems shows that the gel point time may be reached when tan S or loss modulus G" pass a miximum [3,4,13], Some authors proposed to correlate the gel point with the intersection point of the curves of storage and loss moduli, i.e., with the moment at which tan 5 = 1 [14-16], However, theoretical calculations have shown that the intersection point of storage modulus and loss modulus meets the gelation conditions only for a certain law of relaxation behavior of the material and the coincidence erf the moment of equality G = G" with the gel point is a particular case [17]. The variation of the viscosity... [Pg.220]

The determination of equilibrium curves in three-component systems in some respects is simpler than in two-component systems. Consider the diagram in Fig. 15.29. Suppose that the system consists of a solution in equilibrium with solid and that the state point is at a. We do not know the location of a, but we do know that it lies on a tie line connecting the solid composition with the liquid composition. We proceed as follows some of the saturated liquid is removed and analyzed for A and B. This fixes the point s on the equilibrium line. After the removal of some of the saturated solution, the state point of the remainder of the system must lie at point r. So the remainder, that is, the solids together with the supernatant liquid, called the wet residue, is analyzed for two of the components. This analysis determines the point r. A tie line is drawn through s and r. The procedure is repeated on a system that contains a slightly different ratio of two of the components. The solution analysis yields the point 5, while the analysis of the wet residue yields a point r. The tie line is drawn through s and r. These two tie lines must intersect at the composition of the solid that is present. In this system, they would intersect at point D. This intersection point yields the composition of the solid phase D, which is in equilibrium with the liquid. [Pg.342]

To verify that the active PCB and dibenzo-p-dioxin derivatives were interacting with the substrate (rT ) binding site of the enzyme, we investigated the inhibitory mechanism by enzyme kinetic analysis. The results of these experiments are shown in the double reciprocal (Llneweaver-Burk) plot (20) (Fig. 4). A competitive mechanism is strongly suggested by the common intersection point on the vertical axis for the regression lines. The kinetic data derived from this plot for rT are K - 29 nM 70 pmol of... [Pg.361]

The condition (10) allows one to determine regions in the q, p)-plane corresponding to different types of pattern excitation and stability near threshold as shown in Fig.3. The straight hnes OCB and OGF correspond to Ao = 0 and the curves AB, CD, EF, GH are parts of the hyperbola sw/m + Xq = 0. It is interesting that at the intersection point O, p = 1/2, q = 3/4. Since p = 1/2 corresponds to c = 0, this means that unless the wetting potential depends on the film slope the periodic structure is always subcritical and therefore blows up. Weakly nonlinear analysis is not useful in this case. [Pg.131]

Tlie usual procedure for the graphical analysis of initial rate data would be to treat each substrate as the varied substrate at different fixed concentrations of another substrate, maintaining a fixed concentration of the third substrate. All such plots represent a family of straight lines with a common intersection point to the left of the i/Uo-axis. [Pg.218]

A particularly Important example of this Interactive capability occurs in the analysis of time-of-flight diffraction inspection data files. Following display of the set of ultrasonic rf waveforms stored in each file on the colour graphics unit, a screen cursor is used to select points on identified waveforms for display as time-delay ellipses on the appropriate nozzle profile. The intersection point of the arcs generated from the same point on several waveforms corresponds to the location of the defect extremity producing the observed signal. [Pg.316]

The mean length L corresponds to the mean free path along the flow trajectories of the percolation structures. In the absence of a detailed analysis of the frequency distribution of intersection points along these trajectories, we will assume the distribution to be a geometrical one. That means that the mean frequency should be proportional to the density of flow trajectories i.e. the irrigation rate. The mean length L (i.e. [Pg.571]

Fig. 20.14 Working with rheokinetics of polymerization of sodium acrylate (NaAA) and acrylic acid (AA) with different concentration and initiator ratio is 0.8 mmol/mol—raw data by rheometer left), viscosity as a function of time—analysis of the viscosity gradient right) by the use of a reduced time and specific viscosity, see (20.29), dots mark the intersection point of the different fits, see (20.28) mass fraction of acrylates ( ) is equivalent mass fraction related to acrylic acid, where the molar concentration of acrylate and acrylic acid in solution is the same... Fig. 20.14 Working with rheokinetics of polymerization of sodium acrylate (NaAA) and acrylic acid (AA) with different concentration and initiator ratio is 0.8 mmol/mol—raw data by rheometer left), viscosity as a function of time—analysis of the viscosity gradient right) by the use of a reduced time and specific viscosity, see (20.29), dots mark the intersection point of the different fits, see (20.28) mass fraction of acrylates ( ) is equivalent mass fraction related to acrylic acid, where the molar concentration of acrylate and acrylic acid in solution is the same...
Figure 31.1 shows a classic electrochemically measured Tafel polarization diagram [33. The Tafel analysis is performed by extrapolating the linear portions of both cathodic and anodic curves on a log (current) versus potential plot to their point of intersection. This intersection point provides both the corrosion potential con and the corrosion current density for the system unperturbed. This is a very simple yet powerful technique for quantitatively characterizing a corrosion process. The Tafel equation can be simplified to provide Eq. (7) by approximation using a power series expansion. [Pg.886]

As for the variation of the cooling rate, one can try to determine the chain length dependence of the glass transition temperature Tg by looking for the intersection point of the linear extrapolations from the liquid and the glassy region in a plot of the ratio T/Ti versus temperature. The result of this analysis from T, which is presented in Fig. 6.15, yields a linear relationship between the Tg and the inverse chain length as has been claimed by theory" and affirmed in many experiments. ... [Pg.332]

Mechanical-based models for territorial scale analysis on classes of buildings can be defined on the basis of either traditional force-based procedures (e.g., capacity spectrum method implemented in HAZUS, in NIBS (2003), or in RISK-UE (2004)) or according to displacement-based designed approaches (e.g., Calvi et al. 2005). According to force-based procedures, the buUding performance is identified, within acceleration-displacement response spectra (ADRS) by the intersection point between the capacity curve of an equivalent nonlinear SDOF... [Pg.518]


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See also in sourсe #XX -- [ Pg.179 , Pg.180 ]




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Analysis point

Intersect

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