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Equilibration curve

Relaxation kinetics. It is sometimes necessary to cause a larger perturbation, such that the terms in S2 [Eq. (11-8)] cannot be dropped. Can one then ignore the early part of the re-equilibration curve, and fit the later stages as a monoexponential Can one use King s method, as presented in Ref. 3, Chapter 3 ... [Pg.270]

Thus, if we freeze-in the equilibrium at any point along the binding process and then continue the process of binding, the slope of the equilibrated curve will always be steeper than that of the frozen-in curve. [Pg.321]

Plasma base excess is defined as the initial concentration of titratable base when titrating the plasma with strong acid or base to pH (Std) - 7.4 at PCO2 = 40 mm Hg and 37 °C. The equation for the CO2 equilibration curve of plasma and calculation of plasma base excess can be written ... [Pg.1761]

A few years later, in 1977, Boruvka and Neumann [10] published the first rigorous thermodynamic treatment of fully equilibrated, curved interfaces, resulting in a generalized Laplace equation of the kind ... [Pg.555]

Cloud point temperature (CP, determined at 1 K min- ) and coexistence ( determined by refractive index of the low and high polymer concentration phases after 24 h equilibration) curves obtained for a binary mixture of a comb-shaped poly[oligo(2-ethyl-2-oxazoline) methacrylate] in water.The coexistence curve is fitted to guide the eye (Weber et al., 2013). (Source-. Reprinted with permission from Wiley.)... [Pg.20]

In high-pressure processes, often droplets and bubbles are important owing to their high surface area for heat and mass transport. Whereas plane fluid surfaces without external forces are pressure equilibrated, curved interfaces are balanced by the size keeping surface forces and the forces that are acting by the inner pressure in a spherical geometry like a bubble or a droplet with diameter D in equilibrium. [Pg.15]

Figure 2 Equilibration curves for reactions (8) and (17), Table 1, using data in Table 7, Solid lines correspond to average mineral compositions in the lava. The dashed line correspond to maximum and minimum fayalite and albite contents in the respective minerals in the lava. Figure 2 Equilibration curves for reactions (8) and (17), Table 1, using data in Table 7, Solid lines correspond to average mineral compositions in the lava. The dashed line correspond to maximum and minimum fayalite and albite contents in the respective minerals in the lava.
Figure 3 Calculated equilibration curves between a basanite melt and two possible source materials. See Table 7 and text for details. Figure 3 Calculated equilibration curves between a basanite melt and two possible source materials. See Table 7 and text for details.
Surface Micelles. The possibility of forming clusters of molecules or micelles in monolayer films was first proposed by Langmuir [59]. The matter of surface micelles and the issue of equilibration has been the subject of considerable discussion [191,201,205-209]. Nevertheless, many ir-a isotherms exhibit nonhorizontal lines unexplained by equations of state or phase models. To address this, Israelachvili [210] developed a model for ir-u curves where the amphiphiles form surface micelles of N chains. The isotherm... [Pg.134]

The sum expressed by equation (25) also lends itself to a digital solution and can be employed in an appropriate computer program to calculate actual peak profiles for different volumes of pure mobile phase that have been injected onto an equilibrated column. The values of (Xg) were calculated for a column having 500 theoretical plates and for sample volumes of 20, 50, 100 and 200 plate volumes, respectively. The curves relating solute concentration (Xe) to plate volumes of mobile phase passed through the column are shown in Figure 17. [Pg.198]

Based on a lot of experimental observations, criteria for the drop stability can be defined as below the U curve, namely We < We.cn, the interfacial stress can equilibrate the shear stress, and the drop will only deform into a stable prolate ellipsoid. Above this curve, the viscous shear stress becomes larger than the interfacial stress. The drop is at first extended and finally breaks up into smaller droplets. [Pg.691]

Potentiometric titration curves The procedure involves the addition of a salt of a weak acid to the resin and the determination of the pH of the equilibrated solution. Table 9 shows the pK values of the OH groups and dissociation constants of the studied resin. The first ionization occurs at a pH slightly higher than that of sul-... [Pg.780]

The effect of thermal pre-strain treatment on the torsional ductility of the alloys is shown in Figure 9. The curve numbers correspond to the sample series numbers. The basic alloy, a = 0, is represented for comparison as series 4. The series 1 samples had the highest ductility. That of the j9-treated series 2 samples showed a similar thermal dependence below 970 K, but it was lower at 1000 to 1100 K. Ductility of the equilibrated series 3 samples did not show a maximum in its thermal dependence, but it exceeded ductility of the basic alloy. [Pg.433]

A dose-response curve to a full agonist is obtained. A concentration of partial agonist is equilibrated... [Pg.266]

A dose-response curve is obtained to the agonist. Then the same preparation is equilibrated with a... [Pg.267]

Sorption curves obtained at activity and temperature conditions which have been experienced to be not able to alter the polymer morphology during the test, i.e. a = 0.60 and T = 75 °C, for as cast (A) and for samples previously equilibrated in more severe conditions, a = 0.99 and T = 75 °C (B), are shown in Fig. 13. According to the previous discussion, the diffusion coefficient, calculated by using the time at the intersection points between the initial linear behaviour and the equilibrium asymptote (a and b), for the damaged sample is lower than that of the undamaged one, since b > a. The morphological modification which increases the apparent solubility lowers, in fact, the effective diffusion coefficient. [Pg.205]

Gel Filtration. The lyophilized protein was redissolved in 50 mM phosphate buffer, pH 7.4 0.15 m NaCl 0.013 % sodium azide and loaded on a Superdex 75HR1030 column equilibrated with the same buffer. Elution was downward flow (0.15 ml/min) and 0.25 ml fi actions were collected. Fractions with pectin lyase activity were combined, dialyzed against distilled water and used in the next step. To estimate the molecular mass of PNL, the column was calibrated with standard proteins (Sigma MW-GF-70 Albumin, 66,000 Da Carbonic Anhidrase, 29,00 Cytochrome, 12,400 and Aprotinin, 6,500). The proteins were eluted in the conditions described above and their volumes (F ) were calculated fi om the peak maximum of the absorbance at 280 nm. The partition coefficient was obtained fi om the relationship where F, represents the bed volmne of column and F the void volume (which was calculated using blue dextran. Sigma). The molecular mass was determined using a standard curve of vs the logarithm of the molecular masses of the standards [28, 29]... [Pg.750]

As for the theoretical treatment, we could only try to include the eleetrostatie solute-solvent interaetions and, in faet, we corrected the electronic potential energies for the solvation effeets by simply adding as calculated according to the solvaton model [eq. (2)]. The resulting potential curves are to be seen as effective potentials at equilibrium, i.e. refleeting orientational equilibrium distributions of the solvent dipoles around the eharged atoms of the solute molecule. In principle, the use of potentials thus corrected involves the assumption that solvent equilibration is more rapid than internal rotation of the solute molecule. Fig. 4 points out the effects produced on the potential... [Pg.389]

For the experiments in type C catalysts, the pellets were overfilled with cyclohexane and initially cooled to 230 K. They were then reheated in steps of 1 K and allowed to equilibrate for 10 min before each measurement. The signal was determined from 32 accumulations with an echo sequence of 20 ms echo time to ensure that the signal from the plastically crystalline phase of cyclohexane had decayed fully. The typical heating curves of cyclohexane in the fresh and coked catalyst are displayed in Figure 3.3.3(a) As the temperature is increased, larger and... [Pg.269]


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