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Electrolytic cells, experimental

By the time the next overview of electrical properties of polymers was published (Blythe 1979), besides a detailed treatment of dielectric properties it included a chapter on conduction, both ionic and electronic. To take ionic conduction first, ion-exchange membranes as separation tools for electrolytes go back a long way historically, to the beginning of the twentieth century a polymeric membrane semipermeable to ions was first used in 1950 for the desalination of water (Jusa and McRae 1950). This kind of membrane is surveyed in detail by Strathmann (1994). Much more recently, highly developed polymeric membranes began to be used as electrolytes for experimental rechargeable batteries and, with particular success, for fuel cells. This important use is further discussed in Chapter 11. [Pg.333]

In 1839 Alexandre-Edmtmd Becquerel, a French experimental physicist, did the earliest recorded experiments with the photovoltaic effect. Becquerel discovered the photovoltaic effect while experimenting with an electrolytic cell made up of two metal... [Pg.1065]

An electrolysis experiment is performed to determine the value of the Faraday constant (number of coulombs per mole of electrons). In this experiment, 28.8 g of gold is plated out from a AuCN solution by running an electrolytic cell for two hours with a current of 2.00 A. What is the experimental value obtained for the Faraday constant ... [Pg.510]

In order to gain some additional physical insight on how spillover leads to the experimental equations (7.11) and (7.12) we will consider the solid electrolyte cell shown in Figure 7.10a and will examine the situation in absence of spillover (Equations (7.11) and (7.12) not valid) and in presence of spillover (Equations (7.11) and (7.12) valid). For simplicity we focus on and show only the working (W) and reference (R) electrodes which are deposited on a solid electrolyte (S), such as YSZ. The two porous, thus non-blocking, electrodes are made of the same metal or of two different metals, M and M. The partial pressures of 02 on the two sides of the cell are p02 and po2 Oxygen may chemisorb on the metal surfaces so that the work functions w(p02)and R(pb2). [Pg.347]

In summary, the creation via ion spillover of an effective electrochemical double layer on the gas exposed electrode surfaces in solid electrolyte cells, which is similar to the double layer of emersed electrodes in aqueous electrochemistry, and the concomitant experimentally confirmed equation... [Pg.355]

The experimental setup is shown in Figure 9.23. The Pt-black catalyst film also served as the working electrode in a Nafion 117 solid polymer electrolyte cell. The Pt-covered side of the Nafion 117 membrane was exposed to the flowing H2-02 mixture and the other side was in contact with a 0.1 M KOH aqueous solution with an immersed Pt counterelectrode. The Pt catalyst-working electrode potential, Urhe (=Uwr)> was measured with respect to a reversible reference H2 electrode (RHE) via a Luggin capillary in contact with the Pt-free side of the Nafion membrane. [Pg.456]

A laboratory-made electrolytic cell was designed as an electrolytic generator of the molecular hydride of Cd. The influence of several parameters on the recorded signal was evaluated by the experimental design and subsequently optimised univariately... [Pg.304]

Figure 1. Schematic of experimental setup for measurements of the rotating ring-disk electrode (1) dual potentiogal-vanostat (2) ZnO disk electrode (3) Pt ring electrode (4) Teflon electrode holder (5) electrolytic cell (6) N2 gas inlet (7) Pt counter electrode (8) SCE (9) mirror ... Figure 1. Schematic of experimental setup for measurements of the rotating ring-disk electrode (1) dual potentiogal-vanostat (2) ZnO disk electrode (3) Pt ring electrode (4) Teflon electrode holder (5) electrolytic cell (6) N2 gas inlet (7) Pt counter electrode (8) SCE (9) mirror ...
We have extended the technique of Relaxation Spectrum Analysis to cover the seven orders of magnitude of the experimentally available frequency range. This frequency range is required for a complete description of the equivalent circuit for our CdSe-polysulfide electrolyte cells. The fastest relaxing capacitive element is due to the fully ionized donor states. On the basis of their potential dependence exhibited in the cell data and their indicated absence in the preliminary measurements of the Au Schottky barriers on CdSe single crystals, the slower relaxing capacitive elements are tentatively associated with charge accumulation at the solid-liquid interface. [Pg.277]

Use Hardener for platinum and palladinum in jewelry, electrical contact alloys, catalyst, medical instruments, corrosion-resistant alloys, electrodeposited coatings, nitrogen-fixing agent (experimental), solar cells (experimental) the oxide is used to coat titanium anodes in electrolytic production of chloride the dioxide serves as an oxidizer in photolysis of hydrogen sulfide. [Pg.1100]

The experimental study of electrochemical cells contributed in an important way to the acquisition of thermodynamic data for electrolyte solutions. Experimental methods for precisely measuring the EMF of these systems were well established in the first half of the twentieth century [3]. As a result, many data were obtained for electrolyte activities and for important solution equilibria. Some examples of the experiments involved in these studies are given in this section. [Pg.464]

Figure 2.3 Experimental apparatus used by Wehnelt for his studies on electrochemical discharges [119]. The electrolytic cell U with the active electrode and counter-electrode is connected to a capacitor G and an induction coil J. Figure 2.3 Experimental apparatus used by Wehnelt for his studies on electrochemical discharges [119]. The electrolytic cell U with the active electrode and counter-electrode is connected to a capacitor G and an induction coil J.
Thermodynamic data of high accuracy and reliability for the Ni - NiO system at high temperatures were obtained from electrochemical cells with yttria- or calcia-stabilised zirconia electrolytes. The experimental results are in excellent agreement with available calorimetric data as well as emf measurements of previous publications. The recommended Gibbs energy equation for the reaction ... [Pg.425]

The enrichment of tritium is usually determined by the tritium separation (fractionation) factor during electrolysis, and by measuring the initial and final amounts of water. However, many workers have reported that the value of the separation factor of tritium depends on the electrode material, the type of electrolytic enrichment cell, the current density, the mode by which water is fed into the electrolytic cell, and the temperature of the electrolytic cell. In 1991, a reliable method was proposed for estimating tritium concentrations in water, based on a reliable correlation between the water electrolytic enrichment of deuterium and tritium.The constancy of the ratio, k, during the electrolysis, k = a — ) a — 1), was verified experimentally, where a and are the separation... [Pg.1608]

The temperature function is of the type given in Section 25.2.6. It can be experimentally determined using solid-electrolyte cells with solid-state reference electrodes [22]. [Pg.416]

A very interesting application of the classical current interruption technique has been reported by Lorenz and Eichkom [67], who showed that by adopting the galvanostatic configuration it is possible to evaluate the importance of the ohmic drop realistically, point by point, and obtain polarization curves with a trend very close to the ideal one. In fact, it can be experimentally demonstrated that the value of R, is not constant but is influenced by the mass transfer when the current flowing in the electrolytic cell is sufficiently high. In other words, it cannot be excluded a priori that the quantity R, depends on the electrode overvoltage. [Pg.406]


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Electrolytes cells

Electrolytic cell

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