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Spacings salt concentration

Archie [23] examined electrical resistivity of various sand formations having pore spaces filled with saline solutions of different salt concentrations. Based upon his own experimental results, he obtained a simple relationship for the conductivity of beds of sand (assuming the sand itself is nonconductive) containing saline solution in terms of the porosity. In terms of diffusion coefficients his expression is... [Pg.574]

Friant, S.L. and Suffet, I.H. Interachve effects of temperature, salt concentration, and pH on head space analysis for isolahng volatile trace organics in aqueous environmental samples. Anal. Chem., 51(13) 2167-2172, 1979. [Pg.1657]

Dialysis is used to remove lower-molecular components from protein solutions, or to exchange the medium. Dialysis is based on the fact that due to their size, protein molecules are unable to pass through the pores of a semipermeable membrane, while lower-molecular substances distribute themselves evenly between the inner and outer spaces over time. After repeated exchanging of the external solution, the conditions inside the dialysis tube (salt concentration, pH, etc.) will be the same as in the surrounding solution. [Pg.78]

We suggest that the results of calculations described above for a small (Cm < 1 mol liter ) salt concentration give a correct qualitative picture and relevant time/space scales of molecular events. [Pg.289]

Fig. 26 Dissociation of a polymer with N=20 monomers as a function of the distance D from the interface to a low-dielectric half-space (idealized by =0, see text). Shown are degree of dissociation a and free energy per monomer, f/kBT for fixed pH-pKa=5 for different salt concentrations. As the polymer moves towards the interface the degree of dissociation and the free energy approach zero, the polyelectrolyte is repelled from the interface... Fig. 26 Dissociation of a polymer with N=20 monomers as a function of the distance D from the interface to a low-dielectric half-space (idealized by =0, see text). Shown are degree of dissociation a and free energy per monomer, f/kBT for fixed pH-pKa=5 for different salt concentrations. As the polymer moves towards the interface the degree of dissociation and the free energy approach zero, the polyelectrolyte is repelled from the interface...
Fig. 4. The segment concentration distribution between plates for various salt concentrations. Only half space from one plate to the midway is plotted. >=12 A, and the other parameter values used in calculations are as for Fig. 3. (1) c =0.001 M (2) c=0.01 M (3) c=0.1 M (4) c=l M. Fig. 4. The segment concentration distribution between plates for various salt concentrations. Only half space from one plate to the midway is plotted. >=12 A, and the other parameter values used in calculations are as for Fig. 3. (1) c =0.001 M (2) c=0.01 M (3) c=0.1 M (4) c=l M.
Interlayer Spacing d as a Function of Salt Concentration c from Laboratory Experiments... [Pg.88]

Interlayer Spacing d as a Function of Salt Concentration c from Neutron Diffraction Measurements in the Sol Concentration Range r between 0.01 and 0.1... [Pg.92]

FIGURE 9.7 Clay layer spacings d in vermiculite gels as a function of the external salt concentration c for propylammonium (solid circles) and butylammonium (open squares) vermiculites. [Pg.168]

Iv) Cross-differentiation also yields Esin-Markov coefficients p. Introduced in sec. I.5.6d. These coefficients contain information on the relative contributions of the cations and anions to the countercharge, l.e. they help to obtain the composition of the double layer. Experimentally, is measured as the horizontal spacing between ff°(pAg) or salt concentrations and defined as... [Pg.258]

Qualitatively, the phase diagram fits very well to the phase diagram known for single-chain polyelectrolytes, the phase boundaries are only slightly shifted. In principle, the parameter space for polyelectrol ffes has far more dimensions, such as the solvent quality parameter, the valency of monomers or counterions, and additional salt concentration in the system. Especially for multivalent counterions, one can expect an even more complex picture, since correlation effects are known to play an important role even for single chains. [Pg.218]

A well-known phenomenon in inorganic salts is the salting-out effect. Adding sodium sulphate, ammonium sulphate or sodium chloride (common salt), for example, in portions to aqueous systems has the effect of driving out some of the volatile compounds into the gaseous phase, or into a solvent which is immiscible with water. Of the salts mentioned above, only common salt has any relevance to food. Additions of 5 to 15% to aqueous systems result in increases of head space concentration of ethyl acetate, isoamyl acetate and menthone up to 25% [10,32], This common salt concentration, however, is way above what is tolerated normally in foodstuffs. In foods with a normal salt content, the salt has virtually no effect on the vapour pressure of volatile compounds [9,10,32], The same is true for calcium chloride [8[, The possibility, that the salt content of the saliva has some effect on the vapour pressure cannot be ruled out however [32],... [Pg.454]

The waterglass solution reacts with the metal ions to form a scmipcrmcable membrane consisting of an almost insoluble precipitate of metal salts. Since the concentration of the dissolved metal salts is greater in the space between crystal and inemhiane l.lian in ilie surrounding soluiion water diffuses inio ihis space. The osmotic pressure thus increases and the membrane expands or bursts. The hole thus formed is immediately filled by the metal salt. The salt concentration is lowest at the highest point of the membrane, so that the latter normally bursts here and the "plants grow upwards as in nature. [Pg.24]


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See also in sourсe #XX -- [ Pg.10 ]




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