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Electrolytic conductors dissociation

Since Na[Et3Al-F-AlEt3], dissolved in toluene, is a good electrolytic conductor and a considerable proportion of the complex should exist as dissociated ions, an ionic exchange mechanism can be proposed (see Scheme 1). [Pg.183]

Let the electrolysis of dilute sulfuric acid (so-called electrolysis of water) with a platinum cathode and a platinum anode be considered next. Pure water is a very weak electrolyte and consequently a very poor conductor of electricity. It dissociates very slightly into H+ ions (it may be recalled that in fact, H+ ions does not remain as such but forms hydronium in H30+ by combining with a molecule of water, H+ + H20 H30+) and OFT ions. In the presence of little sulfuric acid (or for that matter any other strong electrolyte) the conductivity, i.e., ionization is greatly increased. The acidified water now contains H+ ions, OFT and SC3 ions. During electrolysis with platinum electrodes, H+ ions are attracted to the cathode, where each ion gains an electron and becomes a hydrogen atom ... [Pg.691]

Fig. 3. Oxygen transport in solids. 02 is dissociated and ionized at the reduction interface to give O2 ions, which are transferred across the solid to the oxidation interface, at which they lose the electrons to return back to 02 molecules that are released to the stream, (a) In the solid electrolyte cell based on a classical solid electrolyte, the ionic oxygen transport requires electrodes and external circuitry to transfer the electrons from the oxidation interface to the reduction interface (b) in the mixed conducting oxide membrane, the ionic oxygen transport does not require electrodes and external circuitry to transfer the electrons to the reduction interface from the oxidation interface, because the mixed conductor oxide provides high conductivities for both oxygen ions and electrons. Fig. 3. Oxygen transport in solids. 02 is dissociated and ionized at the reduction interface to give O2 ions, which are transferred across the solid to the oxidation interface, at which they lose the electrons to return back to 02 molecules that are released to the stream, (a) In the solid electrolyte cell based on a classical solid electrolyte, the ionic oxygen transport requires electrodes and external circuitry to transfer the electrons from the oxidation interface to the reduction interface (b) in the mixed conducting oxide membrane, the ionic oxygen transport does not require electrodes and external circuitry to transfer the electrons to the reduction interface from the oxidation interface, because the mixed conductor oxide provides high conductivities for both oxygen ions and electrons.
Role of the bulk transport path. In section 3 we saw that for Pt the dissociation of oxygen and transport of reactive intermediates to the electrode/ electrolyte interface is confined to the material surface. With mixed conductors, it is possible for oxygen reduced at the surface to be transported through the bulk of the material to the electrode/ electrolyte interface. If bulk transport is facile, this path may dominate, extending both the accessible surface for O2 reduction as well as broadening the active charge-transfer area from the TPB to include the entire solid—solid contact area. [Pg.576]

Sensitivity of interfacial resistance to various factors. For perovskite mixed conductors on some ceria-based electrolytes, workers have reported virtually zero interfacial resistance such that the electrode overpotential is dominated entirely by dissociation of O2 and transport of intermediates to the electrode/ electrolyte interface. As we will see in section 6, this conclusion is not universally true of all materials additional impedance arcs have been observed for perovskites on YSZ and with ceria at lower temperatures or with certain electrolyte dopants. [Pg.577]

When ionic salts dissolve in water, the individual ions separate. These positively and negatively charged particles in the water medium are mobile and can move from one part of a solution to another. Because of this movement, solutions of ions can conduct electricity. Electrolytes are substances which can form ions when dissolved in water and can conduct an electric current. These substances are also capable of conducting an electric current in the molten state. Nonelectrolytes are substances which do not conduct an electric current. Electrolytes may be further characterized as either strong or weak. A strong electrolyte dissociates almost completely when in a water solution it is a good conductor of electricity. A weak electrolyte has only a small fraction of its particles... [Pg.174]

The PEFC was first developed for the Gemini space vehicle by General Electric, USA. In this fuel cell type, the electrolyte is an ion-exchange membrane, specifically, a fluorinated sulfonic acid polymer or other similar solid polymer. In general, the polymer consists of a polytetrafluoroethylene (Teflon) backbone with a perfluorinated side chain that is terminated with a sulfonic acid group, which is an outstanding proton conductor. Hydration of the membrane yields dissociation and solvation of the proton of the acid group, since the solvated protons are mobile within the polymer. Subsequently, the only liquid necessary for the operation of this fuel cell type is water [7,8],... [Pg.377]

Solutions of non-electrolytes contain neutral molecules or atoms and are nonconductors. Solutions of electrolytes are good conductors due to the presence of anions and cations. The study of electrolytic solutions has shown that electrolytes may be divided into two classes ionophores and ionogens [134]. lonophores (like alkali halides) are ionic in the crystalline state and they exist only as ions in the fused state as well as in dilute solutions. Ionogens (like hydrogen halides) are substances with molecular crystal lattices which form ions in solution only if a suitable reaction occurs with the solvent. Therefore, according to Eq. (2-13), a clear distinction must be made between the ionization step, which produces ion pairs by heterolysis of a covalent bond in ionogens, and the dissociation process, which produces free ions from associated ions [137, 397, 398]. [Pg.46]

The factor i only occurs in solutions which are good conductors of electricity, and in 1887 Arrhenius succeeded in explaining these apparent deviations from the simple laws by his electrolytic dissociation theory. The molecules of an electrolyte are broken up to a greater or less extent into their free ions, even when the solution is not conducting a current of electricity. Thus we have the equation HCl H - - CL... [Pg.280]

Acids are electrolytes, so their solutions in water are conductors of electric current, as Figure 2 demonstrates. To understand why, consider what happens as hydrogen chloride, HCl, dissolves in water. Like other electrolytes, hydrogen chloride dissociates to produce ions. The hydrogen ion immediately reacts with a water molecule to form a hydronium ion, as shown in the equation below. [Pg.549]

One of the most important practical applications of lithium compounds is as fast ion conductors with potential electronic applications such as solid electrolytes for lithium batteries. Li20 is a fast ion conductor in which the Li ions occupy a simple cubic sublattice with the antifluorite structure. Both MAS and static Li NMR spectra of Li20 have been reported, the former recorded as a function of temperature up to 1000 K (Xie et al. 1995). The effect of introducing vacancies on the Li sites by doping with LiF has been studied by high-temperature static Li NMR, which reveals the interaction of the Li defects > 600 K and the appearance of 2 distinct quadrupolar interactions at about 900 K. Measurements of the relative intensities of the satellite peaks as a function of temperature have provided evidence of thermal dissociation of an impurity-vacancy complex (Xie et al. 1995). [Pg.636]

Experiment 2 Molar Conductivity Measurements Considering Arrhenius s electrolytic theory of dissociation, Werner noted that evidence for his coordination theory may be obtained by determining the electrolytic conductivity of the metal complexes in solution. Werner and Jprgensen assumed that acid (ionic) residues bound directly to the metal would not dissociate and would thus behave as nonconductors, while those loosely held would be conductors. Molar conductivities of 0.1 molar percent aqueous solutions of some tetravalent platinum and trivalent cobalt ammines are given in Table 2.3. [Pg.27]

Electrolyte A substance which undergoes dissociation into ions in solution, and thus acts as a conductor of electricity. [Pg.62]

Recall that solutions of electrolytes are formed from solutes that are soluble ionic compounds. These compounds dissociate in solution to produce ions that behave as charge carriers. Solutions of electrolytes are good conductors of electricity. For example, sodium chloride dissolving in water ... [Pg.178]

In solutions of electrolytes the solutes are ionic compounds that dissociate in solution to produce ions. They are good conductors of electricity. Solutions of nonelectrolytes are formed from nondissociating molecular solutes (nonelectrolytes), and their solutions are nonconducting. [Pg.200]

This process is the autoionization, or self-ionization, of water. Water is therefore a very weak electrolyte and a very poor conductor of electricity. Water has both acid and base properties dissociation produces both the hydronium and hydroxide ion. [Pg.242]

In this experiment the conductivity of some pure liquids is tried, then that of some solutions. It will be found that all solutions do not behave alike in this respect, only those of certain classes of substances being good conductors. Upon this fact and certain other peculiarities of these same substances, which were studied in Experiment 47, the conception of electrolytic dissociation is based. [Pg.114]

ELECTROLYTE SOLUTIONS are solutions of electrolyte compounds in pure or mixed solvents such that the solutions become electric conductors in which current is carried by the movement of ions. They exhibit specific properties due to the more or less complete dissociation of their solutes into ions. Aqueous electrolyte solutions are involved in numerous biological, biochemical, geological, and technical processes. Nonaqueous electrolyte solutions are intensively studied owing to unique properties for their application in various new technologies such as high-energy batteries, electrodeposition, nonemissive displays, solar cells, phase-transfer catalysis, or electroor-ganic synthesis. [Pg.79]

Electrolyte solutions are those in which the solute (e.g., NaCl) dissociates into charged particles called ions (e.g., Na" " and Cr). Naturally, such solutions are much better conductors of electricity than is the solvent alone (normally water), and the conductivity of the solution will depend on the extent to which the dissociation takes place. That is, if only some of the NaCl dissociates into Na+ and Cl , the solution will be less conducting than if all of it does. Measurement of conductivity is therefore a means of determining the degree of dissociation of solutes. Significant improvements in the speed and accuracy of conductance measurements has been achieved by using a flow-through cell (Zimmerman etal. 1995). [Pg.148]

Arrhenius received the 1903 Nobel Prize in chemistry for his work on electrolytes. He found that a solution conducts electricity because the solute dissociates immediately upon dissolving into electrically charged particles (ions). The movement of these ions toward oppositely charged electrodes causes the solution to be a conductor. According to Arrhenius s theory, solutions that are relatively poor conductors contain electrolytes that are only partly dissociated. Arrhenius also believed that ions exist in solution whether or not an electric current is present. In other words, the electric current does not cause the formation of ions. Remember that positive ions are cations negative ions are anions. [Pg.358]

Dilute solutions of diethyl ether show high electric conductivities, but concentrated solutions are poor conductors. The relative proton affinities remain the same and the extent of proton transfer and hence ionization will also remain unaltered, but the degree of electrolytic dissociation is decreased considerably by increased amounts of diethyl ether because of the lowering of the dielectric constant. [Pg.63]


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