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Approach curve

Numerous AFM imaging techniques have been developed and commercialized to monitor topography, friction, mechanical response, capacitance, magnetic properties, etc. However, adhesion measurements require the tip to come into, and out of, contact to measure attractive and adhesion forces. Therefore, other than to select an analysis region, most imaging techniques are not useful for adhesion studies. Instead, measurements are necessarily based on force-displacement curve approaches. [Pg.195]

The term r Vf in Equation (3.71) can be interpreted as a reduced fiber-volume fraction. The word reduced is used because q 1. Moreover, it is apparent from Equation (3.72) that r is affected by the constituent material properties as well as by the reinforcement geometry factor To further assist in gaining appreciation of the Halpin-Tsai equations, the basic equation. Equation (3.71), is plotted in Figure 3-39 as a function of qV,. Curves with intermediate values of can be quickly generated. Note that all curves approach infinity as qVf approaches one. Obviously, practical values of qV, are less than about. 6, but most curves are shown in Figure 3-39 for values up to about. 9. Such master curves for various vaiues of can be used in design of composite materiais. [Pg.157]

Fig. 3 shows a hypothetical case similar to the NH" situation but for which the anion and neutral curves approach closely at longer bond lengths. In this case, one would expect larger rates of detachment than in NH because... [Pg.293]

The anion and neutral curves approach one another at R values that are accessible to the vibrational wavefimctions of the two states shown in Fig. 3, thus allowing strong modulation of the HOMO. [Pg.293]

Plotting the overpotential against the decadic logarithm of the absolute value of the current density yields the Tafel plot (see Fig. 5.3). Both branches of the resultant curve approach the asymptotes for r RT/F. When this condition is fulfilled, either the first or second exponential term on the right-hand side of Eq. (5.2.28) can be neglected. The electrode reaction then becomes irreversible (cf. page 257) and the polarization curve is given by the Tafel equation... [Pg.271]

A comparison of the thus calculated with the measured specific rotations of the 0th- to 4th-generation dendrimers of this kind gave a close resemblance, with a curve, approaching asymptotically a limiting value (Fig. 26). It was also shown that the shape of this curve was independent of solvent, concentration and temperature. This was not the case when CD spectra of these dendrimers were compared (Fig. 27) in solvents such as CH2C12 and f-butyl methyl ether a constant rise of the Cotton effect was observed, which correlates with the increasing amount of benzene chromophores in the dendrimers. However, in the... [Pg.162]

If a reaction is reversible and if one has assumed a rate function that does not take the reverse reaction into account, one observes a downward curvature. As equilibrium is approached, the slope of this curve approaches zero. Another cause of curvature is a change in temperature during the course of the experiment. An increase in temperature causes an increase in the reaction rate, leading to an upward curvature. Bunnett (3) has discussed a number of other sources of curvature, including changes in pH and ionic strength, impurity effects, autocatalysis, and side reactions. [Pg.50]

Note that in this case the right side of equation 11.1.68 is zero for t = 0 and unity for t = 00. Figure 11.9 contains several F(t) curves for various values of n. As n increases, the spread in residence time decreases. In the limit, as n approaches infinity the F(t) curve approaches that for an ideal plug flow reactor. If the residence time distribution function given by 11.1.69 is differentiated, one obtains an... [Pg.406]

Step (18) in the above is the analog of step (8), which is required for H2—D2 equilibration it is a necessary step if we view the jr-allyl as an immobile species on the surface. The products of step (19) can be viewed as propylene in the form of a loosely held w-complex which on desorption yields isomerized propylene. Readsorption of the isomerized propylene or further reaction of the x-complex would yield surface OD groups. When equilibrium is achieved, the concentration of surface OD groups should equal 40% of the initial concentration of OH groups. Figure 21 shows a plot versus time of the intensity (multiplied by a scale factor to yield concentration) of the surface OH and OD. The expected equilibrium points are indicated by arrows. Corresponding data for CD3—CH=CH2 are also shown. Except for the OH species from CD3—CH=CH2, which is a relatively weak band on the side of a surface hydroxyl, the curves approach the expected value. [Pg.39]

Work done by L. Mullins on the prestressing of filler-loaded vulcanisates showed that such prestressing gives a stress-strain curve approaching that of an unfilled rubber. This work has thrown much light on so called permanent set and the theory of filler reinforcement. See Stress Softening. [Pg.42]

The behavior predicted by this equation is illustrated in Fig. 16-33 with N = 80. xF = (evtp/L)/[( 1 - e)(p K, + ,)] is the dimensionless duration of the feed step and is equal to the amount of solute fed to the column divided by tne sorption capacity. Thus, at xF = 1, the column has been supplied with an amount of solute equal to the stationary phase capacity. The graph shows the transition from a case where complete saturation of the bed occurs before elution (xF= 1) to incomplete saturation as xF is progressively reduced. The lower curves with xF < 0.4 are seen to be nearly Gaussian and centered at a dimensionless time xm — (1 — tf/2). Thus, as xF -> 0, the response curve approaches a Gaussian centered at t = 1. [Pg.42]

The Gaussian is a one parameter model, the variance. The RTD curves are bell shaped. At smaller values of the variance (or the larger values of n of the Erlang), the Erlang and Gaussian RTD curves approach each other, and the... [Pg.508]

While this method is extremely simple it is also experimentally inaccurate. Because of the hyperbolic nature of the relationship, the curve approaches maximum velocity asymptotically making the deduction of a value for difficult. Any error in assessing this value will be reflected in the value ascribed to Km. [Pg.264]

The characteristic shape of the anodic voltammogram of a Si electrode in aqueous fluoride media, as shown for example in Fig. 3. Id, is surprisingly stable against changes in fluoride concentration (cF) or pH. When the potential of a p-type Si electrode is swept anodic of OCP a steep current rise near 0 V is observed, followed by a sharp peak (Jj) and a narrow plateau (J2). Then a second broad maximum (Ji) is found around a positive bias of 1.5-2.5 V, followed by a broad plateau (J4) extending over several volts, as shown in Fig. 4.7. When electrode rotation is used, these curves are pen-reproducible for a given solution. The hysteresis of the curves approaches zero for slow sweeps [Ch3]. [Pg.59]

Figure 20.1 Plotting cumulative amount versus time in a Franz-diffusion cell experiment results in a curve approaching a straight line. Figure 20.1 Plotting cumulative amount versus time in a Franz-diffusion cell experiment results in a curve approaching a straight line.
With t -> oo, the linear part of the curve approaches the straight line... [Pg.462]

Equation (38) gives an explanation for the curves reported in different salt solutions At high salt concentration the potential goes to zero and cq- approaches cq-, so that both terms diminish and the titration curve approaches that of a monofunctional acid. At low salt concentrations the potential is high and the Donnan distribution requires ccr >... [Pg.306]

The solid curve in Figure 16.1 shows the activity of the solvent in a solution as a function of the mole fraction of solvent. If the solution were ideal, Equations (14.6) and (16.1) would both be applicable over the whole range of mole fractions. Then, fli =Xi, which is a relationship indicated by the broken line in Figure 16.1. Also, because Equation (16.1) approaches Equation (14.6) in the limit as Xj 1 for the real solution, the solid curve approaches the ideal line asymptotically as Xj 1. [Pg.360]

Figure 3 shows the curves calculated with Eq. (55) for different ratios DA/n, for increasing the curves approach more and more the curve... [Pg.215]

For small deviations from plug flow DluL becomes small, the E curve approaches gaussian hence, on expanding the exponentials and dropping higher order terms Eq. 19 reduces to... [Pg.314]

Fig. 16 Representative f-d curves measured for photograft-polymerized surfaces of DMA after photoirradiation for 10 s, 20 s, 1 min, 5 min, 10 min, and 20 min. Dashed curves Approaching trace, solid curves retracting trace. The repulsion interaction distance increased with photoirradiation time... Fig. 16 Representative f-d curves measured for photograft-polymerized surfaces of DMA after photoirradiation for 10 s, 20 s, 1 min, 5 min, 10 min, and 20 min. Dashed curves Approaching trace, solid curves retracting trace. The repulsion interaction distance increased with photoirradiation time...
Fig. 19 Representative force-versus-distance curves (approach trace) measured on NI-PAAm graft-polymerized surfaces. Solid curves 25 °C, dashed curves 40 °C... Fig. 19 Representative force-versus-distance curves (approach trace) measured on NI-PAAm graft-polymerized surfaces. Solid curves 25 °C, dashed curves 40 °C...
Figure 3.12 shows the variation of F with Xp when FT = 1. As decreases, the curves approach a limiting case solved much earlier, (Nl), often called the Newman solution. This corresponds to negligible external resistance, and Eqs. [Pg.55]

The data of both Price (her Fig 4) and Cook (his p 49) agree that as charge diameter increases, such. curves approach. more closely the ideal curve... [Pg.654]


See other pages where Approach curve is mentioned: [Pg.264]    [Pg.433]    [Pg.1315]    [Pg.22]    [Pg.336]    [Pg.290]    [Pg.102]    [Pg.44]    [Pg.220]    [Pg.299]    [Pg.153]    [Pg.526]    [Pg.264]    [Pg.8]    [Pg.129]    [Pg.67]    [Pg.368]    [Pg.330]    [Pg.150]    [Pg.146]    [Pg.268]    [Pg.379]    [Pg.6]    [Pg.68]    [Pg.62]    [Pg.18]    [Pg.433]   
See also in sourсe #XX -- [ Pg.362 ]




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