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Osmotic pressure INDEX

Molecular weights of polysaccharides in solution can also be measured by osmotic pressure and light scattering. Osmotic pressure yields the number average molecular weight, which can be usefully used with Mw from sedimentation equilibrium as a measure of polydispersity Preston and Wik [28] have done this for example with hyaluronic acid. The ratio Mw/Mn the polydispersity index is often given as a measure of polydispersity, and can be related to the width of a molecular weight distribution via the well-known Herdan [96] relation ... [Pg.234]

The body s normal daily sodium requirement is 1.0 to 1.5 mEq/kg (80 to 130 mEq, which is 80 to 130 mmol) to maintain a normal serum sodium concentration of 136 to 145 mEq/L (136 to 145 mmol/L).15 Sodium is the predominant cation of the ECF and largely determines ECF volume. Sodium is also the primary factor in establishing the osmotic pressure relationship between the ICF and ECF. All body fluids are in osmotic equilibrium and changes in serum sodium concentration are associated with shifts of water into and out of body fluid compartments. When sodium is added to the intravascular fluid compartment, fluid is pulled intravascularly from the interstitial fluid and the ICF until osmotic balance is restored. As such, a patient s measured sodium level should not be viewed as an index of sodium need because this parameter reflects the balance between total body sodium content and TBW. Disturbances in the sodium level most often represent disturbances of TBW. Sodium imbalances cannot be properly assessed without first assessing the body fluid status. [Pg.409]

Analysis of osmotic pressure of semi-diluted polymeric solutions by Scaling method is based [3] on two positions. Accordingly to the first one it is assumed that the polymeric chain is in good solvent for which % < 1 / 2. This position is necessary in order to index v in the expression (2) will be determined by the ratio... [Pg.41]

It is fortunate that theory has been extended to take into account selective interactions in multicomponent systems, and it is seen from Eq. (91) (which is the expression used for the plots in Fig. 42 b) that the intercept at infinite dilution of protein or other solute does give the reciprocal of its correct molecular weight M2. This procedure is a straightforward one whereby one specifies within the constant K [Eq. (24)] a specific refractive index increment (9n7dc2)TiM. The subscript (i (a shorter way of writing subscripts jUj and ju3) signifies that the increments are to be taken at constant chemical potential of all diffusible solutes, that is, the components other than the polymer. This constitutes the osmotic pressure condition whereby only the macromolecule (component-2) is non-diffusible through a semi-permeable membrane. The quantity... [Pg.205]

In these equations ns is the solvent refractive index, dn/dc the refractive index increment, c the polymer concentration in g/ml, T the temperature in K, R the gas constant, NA Avogadro s number, and n the osmotic pressure. Equation (B.8) follows from Eq. (B.7) by using the familiar virial expansion of the osmotic pressure... [Pg.9]

The phenomenon of soil dispersion with respect to Na+ loads (magnitude of ESP or SAR) appears to be unique to all soils on at least one particular point. As the total salt or Cl- concentration in the water increases, the dispersion index decreases and the saturated hydraulic conductivity increases (Fig. 11.6). When this occurs, the soil-water system becomes toxic to plants and organisms owing to high osmotic pressures. When chloride concentration in solution increases beyond 6000 mg L 1, Na ions near clay surfaces begin to dehydrate because of high osmotic pressure in the surrounding solution. This causes clay particles to flocculate (flocculation is the reverse of dispersion) and, consequently, the saturated hydraulic conductivity of the soil increases. [Pg.415]

There is a curious discrepancy in the archives of the Society concerning the General Discussions. In the index of Volume III for 1907 two general discussions are recorded, one on " Osmotic Pressure, one on Hydrates in Solution . Sir OUver Lodge was then President of the Society. In the index to the first twenty volumes of the Transactions the earhest recorded General Discussion is in Volume IV, on The Constitution of Water . [Pg.311]

Pure liquids and solutions have probably received a major portion of the experimental effort devoted to the nonspectroscopic methods of detection. The liquid phase is susceptible to simple techniques and is the naturally occurring state for many substances. The principal methods of study are vapor pressure measurements, cryoscopy, solubility, and partition studies. To a lesser degree parachor, refractive index, thermal and acoustic conductivity, osmotic pressure, and magnetic susceptibility measurements have been applied to H bonded materials. Unfortunately, the difficulty of giving an adequate description of the liquid state sometimes produces problems of interpretation. [Pg.37]

The CMC is also well defined experimentally by a number of other physical properties besides the variation of the surface tension. The variation of solution properties such as osmotic pressure, electrical conductance, molar conductivity, refractive index, intensity of scattered light, turbidity and the capacity to solubilize hydrocarbons with the increase of surfactant concentration will change sharply at the CMC as shown in Figure 5.8. The variation in these properties with the formation of micelles can be explained as follows. When surfactant molecules associate in solution to form micelles, the concentration of osmotic units loses its proportionality to the total solute concentration. The intensity of scattered light increases sharply at the CMC because the micelles scatter more light than the medium. The turbidity increases with micelle formation, because the solution is transparent at low surfactant concentrations, but it turns opaque after the CMC. Hydrophobic substances are poorly dissolved in aqueous solutions at concentrations below the CMC, but they start to be highly dissolved in the centers of the newly formed micelles, after the CMC. [Pg.204]

This gives the equation correlating the mean square value of the fluctuation of polarizability with the corresponding fluctuation in the concentration. It is apparent that the proportionality factor relating these two quantities depends both on the square of the refractive index of the medium and on the square of the refractive increment of the solute. Details of the derivation may be found elsewhere (see for instance Zimm, Stein and Doty, 1945). The final equation, as given by Einstein, furnishes a direct correlation between the turbidity produced by the solute and the change of its osmotic pressure (P) with concentration. [Pg.9]

Fig. 2. Influence of the formation of micelles on the properties of Na dodecylsulphate at 20 and 25 C. (HF — conductivity for high frequency current, P == osmotic pressure, y Voo = conductivity coefficient, = surface tension, rjrei — relative viscosity, = change of specific volume, In = change of refractive index). From Hess, Philippoff, and Kiessig, 1939. Fig. 2. Influence of the formation of micelles on the properties of Na dodecylsulphate at 20 and 25 C. (HF — conductivity for high frequency current, P == osmotic pressure, y Voo = conductivity coefficient, = surface tension, rjrei — relative viscosity, = change of specific volume, In = change of refractive index). From Hess, Philippoff, and Kiessig, 1939.
Because chemical fertilizers are salts, the overapplication of soluble fertilizers can cause the soil solution to have high osmotic pressure and inhibit water uptake by seeds or plants. For this reason, soluble fertilizers (mainly the N and K forms) cannot be applied in large amounts with seeds or close to plants. A salt index was developed years ago to pro e relative guid-... [Pg.37]


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