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Solutes molarity

Figure Bl.22.8. Sum-frequency generation (SFG) spectra in the C N stretching region from the air/aqueous acetonitrile interfaces of two solutions with different concentrations. The solid curve is the IR transmission spectrum of neat bulk CH CN, provided here for reference. The polar acetonitrile molecules adopt a specific orientation in the air/water interface with a tilt angle that changes with changing concentration, from 40° from the surface nonnal in dilute solutions (molar fractions less than 0.07) to 70° at higher concentrations. This change is manifested here by the shift in the C N stretching frequency seen by SFG [ ]. SFG is one of the very few teclnhques capable of probing liquid/gas, liquid/liquid, and even liquid/solid interfaces. Figure Bl.22.8. Sum-frequency generation (SFG) spectra in the C N stretching region from the air/aqueous acetonitrile interfaces of two solutions with different concentrations. The solid curve is the IR transmission spectrum of neat bulk CH CN, provided here for reference. The polar acetonitrile molecules adopt a specific orientation in the air/water interface with a tilt angle that changes with changing concentration, from 40° from the surface nonnal in dilute solutions (molar fractions less than 0.07) to 70° at higher concentrations. This change is manifested here by the shift in the C N stretching frequency seen by SFG [ ]. SFG is one of the very few teclnhques capable of probing liquid/gas, liquid/liquid, and even liquid/solid interfaces.
Component 1 is the diffusing gas, while component 2 is the solvent. The solvent viscosity l2 in Pa sec, the solute molar volume at the normal boihng point Vi in mVkmole, and the solvent association parameter Xo multiplied by the solvent... [Pg.415]

The composition of the test solution should be controlled to the billest extent possible and be described as thoroughly and as accurately as possible when the results are reported. Minor constituents should not be overlooked because they often affect corrosion rates. Chemical content should be reported as percentage by weight of the solution. Molarity and normality are also nelpbil in defining the concentration of chemicals in the test solution. The composition of the test solution should be checked by analysis at the end of the test to... [Pg.2426]

Step 1 Convert the observed osmotic pressure into solute molarity (not molality) by writing Eq. 6 in the form... [Pg.457]

The Stokes-Einstein equation predicts that DfxITa is independent of the solvent however, for real solutions, it has long been known that the product of limiting interdiffusion coefficient for solutes and the solvent viscosity decreases with increasing solute molar volume [401]. Based upon a large number of experimental results, Wilke and Chang [437] proposed a semiempirical equation,... [Pg.580]

As described in Section 3-, molarity is the most common concentration measure for aqueous solutions. Molarity (M, units of mol/L) is the number of moles of a solute divided by the volume of solution ... [Pg.831]

Osmotic pressure plays an important role in biological chemistry because the cells of the human body are encased in semipermeable membranes and bathed in body fluids. Under normal physiological conditions, the body fluid outside the cells has the same total solute molarity as the fluid inside the cells, and there is no net osmosis across cell membranes. Solutions with the same solute molarity are called isotonic solutions. [Pg.864]

For any aqueous strong base, the hydroxide ion concentration can be calculated directly from the overall solution molarity. As is the case for aqueous strong acids, the hydronium and hydroxide ion concentrations are linked through the water equilibrium, as shown by Example. ... [Pg.1212]

Figure 5.19 Room temperature emission spectra ofiAuiP P)] (CIO4) in the presence of PPh3 in degassed acetonitrile solution. Molar ratio of PPh3 [Au(P P)] =X 1. Inset a plot ofthe emission intensityofiAuiP P)(PPh3)] vs.X l (concentrationofiAuiP P)] (CIO4) = 10 mol dm ). Reproduced with permission from [12b]. Copyright (1998) Royal Society of Chemistry. Figure 5.19 Room temperature emission spectra ofiAuiP P)] (CIO4) in the presence of PPh3 in degassed acetonitrile solution. Molar ratio of PPh3 [Au(P P)] =X 1. Inset a plot ofthe emission intensityofiAuiP P)(PPh3)] vs.X l (concentrationofiAuiP P)] (CIO4) = 10 mol dm ). Reproduced with permission from [12b]. Copyright (1998) Royal Society of Chemistry.
Upon meltdown a purple solution was obtained. After addition of nitrogen the solution was allowed to warm for another 0.5 hr to room temperature. The solution was syphoned out under N into Schlenk ware. Based on Au evaporated and acetone inlet the solution molarity could be calculated. [Pg.260]

Now we can employ equation 19.4 to calculate the molar solubility of Mg(OH)2 in the buffer solution Molar Solubility Mg(OH)2 = [Mg2+]equii... [Pg.455]

Using the molar mass, calculate the moles of all weighed samples. The moles of substances are converted to molarities by dividing by the volume (in liters) of the solution. Molarities may also be determined from pipet or buret readings using the dilution equation. (If a buret is used, one of the volumes is calculated from the difference between the initial and final readings.) The dilution equation may be needed to calculate the concentration of each reactant immediately after all the solutions are mixed. [Pg.291]

Reagent is aged homogeneous ether solution. Molar ratio LAH 90 ketone = 1.0 2.30 0.21 reaction at room temperature. Determined by GC of MTPA ester, Yield of product 83%. [Pg.269]

Keywords. Solution properties. Regularly branched structures. Randomly and hyperbranched polymers. Shrinking factors. Fractal dimensions. Osmotic modulus of semi-di-lute solutions. Molar mass distributions, SEC/MALLS/VISC chromatography... [Pg.113]

In Table 3 are the values of surface tension for the aqueous LAS homolog solutions. Values of molar volume used are those for the pure LAS homolog independent of water. The justification for this comes from the Winsor R model (20, 21) and work by Scriven and Davis (30) who showed that accurate CED values can be obtained from a statistical mechanical treatment of an interface using only 2 or 3 atomic or molecular layers of that interface. For a surfactant solution, the surfactant will predominate in the interface, hence the choice of pure LAS for the solution molar volumes. [Pg.260]

Similarly, concentration and mole fractions can be related. If p is the density of the solution then, for a solution containing two components A and B, Xb = cb/ [(lOOOp cbMbIMa] + Cb. In dilute aqueous solutions, molarity is approximately equal to molality. See Concentration Range Selection... [Pg.163]

Concentrations of Reactants in Solution Molarity Avogadro s Number A Ballpark Calculation... [Pg.75]

As indicated by the flow diagram in Figure 3.5, using molarity is critical for carrying out stoichiometry calculations on substances in solution. Molarity makes it possible to calculate the volume of one solution needed to react with a given volume of another solution. This sort of calculation is particularly important in acid-base chemistry, as shown in Worked Example 3.14. [Pg.94]


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See also in sourсe #XX -- [ Pg.109 , Pg.110 ]

See also in sourсe #XX -- [ Pg.196 , Pg.490 , Pg.492 , Pg.495 ]




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