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Electrical charges of ions

The last type of column used in liquid chromatography is the column used for ion pair chromatography. In this method an ionic solvent, which has the opposite charge to the sample compound, is used as the mobile phase. The use of such a mobile phase leads to the formation of an ion pair, which is the material eventually analyzed in this method. Samples which cannot be analyzed by adsorption or distribution chromatography because of the high electrical charge of ions, should be analyzed by this method. [Pg.102]

The composition of body fluids remains relatively constant despite the many demands placed on the body each day. On occasion, these demands cannot be met, and electrolytes and fluids must be given in an attempt to restore equilibrium. The solutions used in the management of body fluids discussed in this chapter include blood plasma, plasma protein fractions, protein substrates, energy substrates, plasma proteins, electrolytes, and miscellaneous replacement fluids. Electrolytes are electrically charged particles (ions) that are essential for normal cell function and are involved in various metabolic activities. This chapter discusses the use of electrolytes to replace one or more electrolytes that may be lost by the body. The last section of this chapter gives a brief overview of total parenteral nutrition (TPN). [Pg.633]

We can draw conclusions regarding deformation of ions from observations of the diamagnetic susceptibility just as from those of the mole refraction. Thus in the series C03 , N03 and PO, SO4" the experimental values of / show successively greater deviations from the theoretical ones (assuming undeformed 0= ions) with increasing electrical charge of the central ion. ... [Pg.701]

Total Ionization—The total electric charge of one sign on the ions produced by radiation in the process of losing its kinetic energy. For a given gas, the total ionization is closely proportional to the initial ionization and is nearly independent of the nature of the ionizing radiation. It is frequently used as a measure of absorption of radiation energy. [Pg.278]

In view of the electrostatic nature of forces that primarily lead to deviation of the behaviour of electrolyte solutions from the ideal, the activity coefficient of electrolytes must depend on the electric charge of all the ions present. G. N. Lewis, M. Randall and J. N. Br0nsted found experimentally that this dependence for dilute solutions is described quite adequately by the relationship... [Pg.20]

As mentioned above, a substantial part of the electrical charge of the micelle surface has been shown to be neutralized by the association of the counter ions with the micelle. In the calculation based on Equation 12, however, the loss in entropy arising from this counter ion association is not taken into account. This is by no means insignificant in comparison to of Equation 12 (4). A major part of the counter ions are condensed on the ionic micelle surface and counteract the electrical energy assigned to the amphiphilic ions on the micellar surface. The minor part of the counter ions,in the diffuse double layer, are also restricted to the vicinity of the micellar surface. [Pg.81]

Electric potential differences are formed at the boundary between two phases, at least one of which contains electrically-charged species (ions, electrons, or even dipoles). These differences are of two basic types. The inner potential of a given phase a, 0(a), is the electrical work required for transfer of a unit... [Pg.14]

We now come to internal metal contacts in ISEs without an internal solution. As discussed above, systems without internal electrolytes are used very often, with both solid and liquid membranes. Obviously, the condition of thermodynamic equilibrium requires that common electrically-charged particles (ions or electrons) be present in electrically-charged phases that are in contact (see chapter 2). ISEs with a silver halide membrane to which a silver contact is attached are relatively simple. In the system... [Pg.70]

The concentrations of sodium, potassium (and chloride) ions in the body are high and make the largest contribution to the electrical charge of cells hence they are known as electrolytes. They have two important roles maintenance of the total solute concentration in the cell which prevents excessive movement of water into or out of cells through osmosis and the controlled movement of these ions across cell membranes acts as a signalling mechanism (e.g. the action potential in neurones and muscle. Chapter 14). Severe disruption of sodium or potassium levels in the body interferes with this signalling mechanism and with osmotic balance in cells. [Pg.345]

When particles or large molecules make contact with water or an aqueous solution, the polarity of the solvent promotes the formation of an electrically charged interface. The accumulation of charge can result from at least three mechanisms (a) ionization of acid and/or base groups on the particle s surface (b) the adsorption of anions, cations, ampholytes, and/or protons and (c) dissolution of ion-pairs that are discrete subunits of the crystalline particle, such as calcium-oxalate and calcium-phosphate complexes that are building blocks of kidney stone and bone crystal, respectively. The electric charging of the surface also influences how other solutes, ions, and water molecules are attracted to that surface. These interactions and the random thermal motion of ionic and polar solvent molecules establishes a diffuse part of what is termed the electric double layer, with the surface being the other part of this double layer. [Pg.127]

A multiple-atom molecule or ion must have oxidation numbers that sum to the electrical charge of the group of atoms. A neutral molecule has oxidation numbers adding to zero. Therefore, the oxidation numbers of the 1 nitrogen and 3 hydrogen atoms of the neutral NH3 ammonia molecule sum to 0 ... [Pg.113]

In order to consider the influence of the ionic atmosphere on the electrophoretic mobility, the theoretical electrical charge of the ion q in Equation 6.14 is replaced by the smaller effective charge <2eff and the hydrodynamic radius r by the effective radius R of the ion, which includes its ionic atmosphere ... [Pg.162]


See other pages where Electrical charges of ions is mentioned: [Pg.1756]    [Pg.331]    [Pg.1802]    [Pg.578]    [Pg.259]    [Pg.482]    [Pg.735]    [Pg.206]    [Pg.228]    [Pg.228]    [Pg.1756]    [Pg.331]    [Pg.1802]    [Pg.578]    [Pg.259]    [Pg.482]    [Pg.735]    [Pg.206]    [Pg.228]    [Pg.228]    [Pg.1775]    [Pg.173]    [Pg.95]    [Pg.175]    [Pg.265]    [Pg.232]    [Pg.510]    [Pg.5]    [Pg.708]    [Pg.14]    [Pg.231]    [Pg.46]    [Pg.514]    [Pg.26]    [Pg.442]    [Pg.439]    [Pg.4]    [Pg.90]    [Pg.114]    [Pg.446]    [Pg.401]    [Pg.376]    [Pg.210]    [Pg.231]    [Pg.91]    [Pg.134]    [Pg.161]    [Pg.97]    [Pg.158]   
See also in sourсe #XX -- [ Pg.49 , Pg.73 , Pg.74 ]




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