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Solute concentration, average

For predic ting diffiisivities in binary polar or associating liquid systems at liign solute dilution, the method of Wilke and Chang " defined in Eq. (2-156) can be utilized. The Tyn and Cains equation (2-152) can be used to determine the molar volume of the solute at the normal boihng point. Errors average 20 percent, with occasional errors of 35 percent. The method is not considered to be accurate above a solute concentration of 5 mole percent. [Pg.415]

I. Turbulent, local flat plate, natural convection, vertical plate Turbulent, average, flat plate, natural convection, vertical plate Nsk. = — = 0.0299Wg=Ws = D x(l + 0.494W ) )- = 0.0249Wg=W2f X (1 + 0.494WE )- [S] Low solute concentration and low transfer rates. Use arithmetic concentration difference. Ncr > 10 " Assumes laminar boundary layer is small fraction of total. D [151] p. 225... [Pg.606]

There are, in fact, two reasons why we should prefer to discuss proton transfers of class I. In concentrated solutions the average electrostatic forces between the ions will be intense. Only in proton transfers of class I does the number of positive and negative charges in the solution remain unaltered when the proton is transferred only here do we find the possibility that the contribution from the interionic forces will remain almost unchanged in a proton transfer. At the same time, although the number... [Pg.240]

Initiator concentration in stock solution. Monomer concentration in stock solution. Number average molecular weight. [Pg.264]

The dynamics for each solute concentration study were run 10 times and averaged for each 10 iteration periods. Water molecules from the upper and lower compartments, within the membrane, are designated Wi and W2, respectively. It can be seen from these results that the presence of solutes in the lower compartment, W2, retards the flow of water into the membrane, relative to the flow from the upper compartment, Wi. In addition, this retardation of flow increases as the concentration of solute in W2 increases. We anticipate that these results are comparable to the situation at the earliest manifestation of the osmotic effect [5]. [Pg.102]

Several boundary conditions have been used to prescribe the outer limit of an individual rhizosphere, (/ = / /,). For low root densities, it has been assumed that each rhizosphere extends over an infinite volume of. soil in the model //, is. set sufficiently large that the soil concentration at r, is never altered by the activity in the rhizosphere. The majority of models assume that the outer limit is approximated by a fixed value that is calculated as a function of the maximum root density found in the simulation, under the assumption that the roots are uniformly distributed in the soil volume. Each root can then extract nutrients only from this finite. soil cylinder. Hoffland (31) recognized that the outer limit would vary as more roots were formed within the simulated soil volume and periodically recalculated / /, from the current root density. This recalculation thus resulted in existing roots having a reduced //,. New roots were assumed to be formed in soil with an initial solute concentration equal to the average concentration present in the cylindrical shells stripped away from the existing roots. The effective boundary equation for all such assumptions is the same ... [Pg.337]

In turbulent flow, properties such as the pressure and velocity fluctuate rapidly at each location, as do the temperature and solute concentration in flows with heat and mass transfer. By tracking patches of dye distributed across the diameter of the tube, it is possible to demonstrate that the liquid s velocity (the time-averaged value in the case of turbulent flow) varies across the diameter of the tube. In both laminar and turbulent flow the velocity is zero at the wall and has a maximum value at the centre-line. For laminar flow the velocity profile is a parabola but for turbulent flow the profile is much flatter over most of the diameter. [Pg.5]

Each solvent used was observed to contain no impurities which fluoresce in the spectral region of interest. All solution concentrations used were in the range 10-5 to 10 4 M. Polymer films were cast onto quartz plates from either chloroform or dichloromethane solutions containing 4% (wt/wt) of polymer. The films were air dried at room temperature and had an average thickness of 65 10 )lm. The absorption spectra of the polymer films were measured using an appropriate PMMA or PS film as the reference. [Pg.61]

Figure 14.5 Dependence of the average distance between dendrimer centers on dendrimer solution concentration, . Interpenetration of neighboring den-drimers occurs when this distance becomes shorter than 2/ H (according to ref. [27])... Figure 14.5 Dependence of the average distance between dendrimer centers on dendrimer solution concentration, <j>. Interpenetration of neighboring den-drimers occurs when this distance becomes shorter than 2/ H (according to ref. [27])...
One of them assumes the possibility of a compression of polymer coils at average concentrations down to the dimensions less than in the -solvent. The alternative is based on the existence of the wide distribution of macromolecule dimensions in any time.It is rather natural to assume an increase of the probability of intramolecular reaction with an increase of the dimensions of the macromolecule.. e. more extended conformations go to the gel-fraction and more coiled remain in the sol. With the increase of solution concentration the distances between coils are diminished and the critical dimensions, necessary for a transition into the gel are decreased too. This process will be accompanied by a decrease of the average dimensions of molecules in sol. [Pg.35]

The measurement of the width of the metastable zone is discussed in Section 15.2.4, and typical data are shown in Table 15.2. Provided the actual solution concentration and the corresponding equilibrium saturation concentration at a given temperature are known, the supersaturation may be calculated from equations 15.1-15.3. Data on the solubility for two- and three-component systems have been presented by Seidell and Linkiv22 , Stephen et alS23, > and Broul et a/. 24. Supersaturation concentrations may be determined by measuring a concentration-dependent property of the system such as density or refractive index, preferably in situ on the plant. On industrial plant, both temperature and feedstock concentration can fluctuate, making the assessment of supersaturation difficult. Under these conditions, the use of a mass balance based on feedstock and exit-liquor concentrations and crystal production rates, averaged over a period of time, is usually an adequate approach. [Pg.838]

In Equation 7, solute concentrations are area averaged with the subscripts referring to the mobile or stationary phase, I Is the length of the dead end pores, and the dlffuslvltles and D... [Pg.9]


See other pages where Solute concentration, average is mentioned: [Pg.346]    [Pg.331]    [Pg.346]    [Pg.331]    [Pg.640]    [Pg.158]    [Pg.10]    [Pg.1364]    [Pg.135]    [Pg.267]    [Pg.164]    [Pg.372]    [Pg.121]    [Pg.201]    [Pg.60]    [Pg.283]    [Pg.53]    [Pg.230]    [Pg.343]    [Pg.33]    [Pg.121]    [Pg.286]    [Pg.72]    [Pg.575]    [Pg.243]    [Pg.340]    [Pg.293]    [Pg.458]    [Pg.847]    [Pg.48]    [Pg.267]    [Pg.49]    [Pg.264]    [Pg.86]    [Pg.526]    [Pg.121]    [Pg.234]    [Pg.323]   
See also in sourсe #XX -- [ Pg.60 ]




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Concentrated solutions

Concentrating solutions

Concentration average

Concentration averaging

Solute concentration

Solutions averages

Solutions solution concentrations

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