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Solutes ideal

The McMillan-Mayer theory offers the most usefiil starting point for an elementary theory of ionic interactions, since at high dilution we can incorporate all ion-solvent interactions into a limitmg chemical potential, and deviations from solution ideality can then be explicitly coimected with ion-ion interactions only. Furthemiore, we may assume that, at high dilution, the interaction energy between two ions (assuming only two are present in the solution) will be of the fomi... [Pg.575]

Here the difficulty is to determine the Y, which depend on thex,. This problem has not been solved for the general case. Two courses are open the first is experiment the second, assumption of solution ideality. In the latter case, Y = 1, and Eq. (4-346) reduces to... [Pg.542]

The pH at which basic iron(III) formate begins to precipitate depends upon several factors, which include the initial iron and chloride concentration a high concentration of ammonium chloride is essential to prevent colloid formation. It is important to use an optimum initial pH to avoid a large excess of free acid, which would have to be neutralised by urea hydrolysis, and yet there must be present sufficient acid to prevent the formation of a gelatinous precipitate prior to boiling the solution ideally, a turbidity should appear about 5-10 minutes... [Pg.457]

Solution Ideal gas behavior is a reasonable approximation for the feed stream. The inlet concentrations are 287mol/m of methane and 15mol/m of carbon dioxide. The column pressure drop is mainly due to the liquid head on the trays and will be negligible compared with 8 atm unless there are an enormous number of trays. Thus, the gas flow rate F will be approximately constant for the column as a whole. With fast reaction and a controlling gas-side resistance, c = 0. The gas-phase balance gives everything that is necessary to solve the problem ... [Pg.395]

Solution Ideally, the scaleup will maintain the same inlet concentrations for the two phases, the same relative flow rates and holdups for the two phases, and the same ratio of gas transferred to liquid throughput. It is also necessary to maintain a constant residence time in the liquid phase. It is simple to set the flow rates ... [Pg.428]

Determining whether absorption is related to the formulation or to an intrinsic property of the molecule can be obtained by comparing absorption from a solid formulation and an oral solution, ideally with an IV solution as a reference. [Pg.770]

Activity coefficient — 1 when solution — ideal solution, i.e. very dilute solution. [Pg.186]

AG°m (pure hquid is the standard state for each substance) is 1194 J tnol at 0°C. In a solution containing only the two isomers, equilibrium is attained when the mole fraction of the 3-methylhexane is 0.372. Is the equihbrium solution ideal Show the computations on which your answer is based. [Pg.335]

The normal way of determining recoveries is to spike analyte standards into a blank sample matrix (one not containing the analyte) and compare these with standard solutions. The best way to obtain such a blank sample is to synthesise the API using a different route that cannot give rise to the impurity to be measured. Alternatively, a sample can be highly purified to eliminate the analyte. Such a blank sample may not be available, in which case standard addition may be required. Here, different levels of the analyte are spiked into the sample and the response can be measured from the slope of the resulting line. This can be compared with the results from standard solutions. Ideally, recoveries will be more than 80%, although in difficult analyses this may not always be achievable. [Pg.118]

The osmotic pressure can be measured accurately for colloidal solutes, and one molecular parameter of interest that is readily determined by osmometry is the number average molecular weight of the solute. Molecular weights determined by osmometry are absolute values no calibration with known standards or any assumed theoretical models is required. Even the assumption of solution ideality is not a problem, since results are extrapolated to zero solute concentration before calculations are made. [Pg.106]

The attentive student may be concerned that the concept of ideal solution as introduced in Chapter 6 is possibly inconsistent with the usage of that term as defined in (7.45a-c). However, Sidebar 7.8 demonstrates that these definitions of solution ideality are in fact consistent. We may therefore regard chemical potential-based definitions of binary solution ideality [cf. (6.57)],... [Pg.240]

Solution ideality was previously defined [cf. (6.57)] in terms of the relationship between chemical potential and mole fraction ... [Pg.240]

Second, Raoult s equation is based on the assumption that the liquid behaves as an ideal solution. Ideal-solution behavior is approached only if the components of the liquid mixture are very similar chemically and physically. [Pg.354]

The combination of properties discussed above makes the transition metal carbides, nitrides, and their solid solutions ideal materials for applications requiring rigidity and resistance to deformation, abrasive wear, and corrosion. [Pg.26]

The potential of the ion-selective electrode is generally monitored relative to the potential of a reference electrode. Since the potential of the reference electrode is fixed, and the activity of the ion in the inner solution is constant, the measured cell potential reflects the potential of the ISE, and can thus be related to the activity of the target ion in the sample solution. Ideally, the response of the ISE should obey the following equation... [Pg.168]

Like gases, solutions can also be thought of as ideal. Raoult s law only works for ideal solutions. Ideal solutions are described as those solutions that follow Raoult s law. Solutions that deviate from Raoult s law are nonideal. What makes a solution deviate from ideal behavior The main reason is intermolecular attractions between solute and solvent. When the attraction between solute and solvent is very strong, the particles attract each other a great deal. This makes it more difficult for solute particles to enter the vapor phase. As a result, fewer particles will enter that state and the vapor pressure will be lower than expected. Remember, Raoult s law operates on the assumption that the reason for a decrease in the number of particles leaving the solution is that fewer can be on the surface in order to leave. If, in addition to this, the solute particles are also holding more tightly to the solvent particles, then fewer will leave the surface than expected. The most ideal solutions are those where the solvent and solute are chemically similar. [Pg.205]

The ideal gas, consisting of molecules with zero volume that do not intera fulfills the conditions of solution ideality as a special case. When ideal gases mixed, there is no volume change of mixing, because the molar volume of mixture V B and the molar volumes of the pure species Vf are all equal to RT/... [Pg.162]

Equations (12.46) and (12,47) imply two models of solution ideality. first is based on the Lewis/ Randall rule, for which the standard-state fuga... [Pg.212]

This equation relates the excess Gibbs energy based on the asymmetric treatme of solution ideality to the excess Gibbs energy based entirely on the Lewis Randall rule. [Pg.216]

Figure 12.22 Plots showing the excess Gibbs energy and activity coefficients based on the as treatment of solution ideality. Figure 12.22 Plots showing the excess Gibbs energy and activity coefficients based on the as treatment of solution ideality.
The recommended unit for MCD spectroscopy, Aem, is based on the extinction coefficient for differential absorbance of a 1M solution of the solute at a field strength of 1 T. The original 9 ellipicity unit is still sometimes used. The conversion factors are 6 = 32.98 AA, where 9 is expressed in units of mdeg or [0]m = 3298A6m where, [0]m is expressed in units of deg cm -dmol . Room temperature spectral measurements are usually measured in solution, ideally in a solvent which is optically transparent in the 280-1000 nm region. [Pg.6070]

Stir vigorously the solution at room temperature for 12 h to incorporate atmospheric oxygen into the solution. Ideally, disulfide bridge formation should be monitored by reverse phase HPLC. Purification (step 4) should be performed immediately after the end of the reaction. [Pg.19]

The purpose of this technique is to assess the value of your current solutions against those of your competitors—and relative to an ideal state in which a theoretical solution could fulfill all desired outcomes and avoid all undesired outcomes. Such an idealized solution (ideal innovation) would meet all expectations, cost nothing, and have zero chance of harming the user, anyone else, or the environment. [Pg.15]


See other pages where Solutes ideal is mentioned: [Pg.142]    [Pg.135]    [Pg.125]    [Pg.100]    [Pg.9]    [Pg.240]    [Pg.69]    [Pg.129]    [Pg.7]    [Pg.193]    [Pg.191]    [Pg.216]    [Pg.362]    [Pg.240]    [Pg.147]    [Pg.111]    [Pg.184]    [Pg.265]   
See also in sourсe #XX -- [ Pg.498 ]




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