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Anode, electrochemical reactions

For anodic processes there are also two wave steps on the polarisation curves at potentials cpi and 92 corresponding to two electrochemical reactions. The first anodic electrochemical reaction for sulphide at the potential (pi corresponds to its anodic decomposition (transition of ions of metals in solution),... [Pg.57]

For determination of transient coefficient kioo values, Ryss (1973, 1983) used tens of known deposits with different mineral compositions, at different depths and in different geological situations, but with known geological surface So, mineral concentration Cj and Iiin, i values, which were obtained by CPC polarisation curves for each ore body. It was found that for cathodic electrochemical reactions, on average, k oo = 500 m /A and for the anodic electrochemical reactions kioo = 200 m A for pH>5 (in dry regions) and k oo = 100 mVA for pH<5 (in wet regions). [Pg.66]

The anodic electrochemical reactions which can occur following the reverse of Reaction 8 are the oxidation of sulfide, present in the bulk electrolyte, to polysulfide the oxidation of polysulfide to hypersulfide and/or sulfur and the oxidation of hypersulfide (which could form either... [Pg.204]

These processes represent the first anodic electrochemical reaction (FAER), which can he expressed hy the following overall equation ... [Pg.91]

When this reaction proceeds, the active centres are blocked by (OH)° radicals and the electrode is passivated. Upon increase of the potential above a value (ps), the second anodic electrochemical reaction (SAER) begins ... [Pg.91]

In the active region, the anodic electrochemical reaction is metal oxidation. Mixed potential theory governs the alloy corrosion in this r on. The corrosion potential and... [Pg.6]

SSEM is novel mode of using an anodic electrochemical reaction at the microcontact between the ion conducting microelectrode and metal substrate as a result of the continuous application of DC electric field. The metal substrate is locally incorporated into the ionic conductor in the form of metal ions through the microcontact [7]. The method can easily control the machining size and depth by adjusting the contact areas, i.e., shape of the apex or other electrochemical machining parameters. [Pg.222]

By definition, power expressed in watts is equal to amperes x volts, and energy expressed in watt-hours is equal to amperes x volts x time (in hours). Therefore, the calculation of energy consumption requires a knowledge of the overall reaction and the number of Faradays required to produce the desired product, the operating cell voltage, and the cell current efficiency, which is illustrated here for the case of electrolytic chlorine production. The main anodic electrochemical reaction during the electrolysis of brine is the discharge of the chloride ions to produce chlorine, as described by reaction (4). When the chlorine current efficiency, ci2> is 100%, one Faraday of electricity will produce... [Pg.165]

FIG. 1— Application of mixed potential theory showing the electrochemical potential-current relationship for a corroding system consisting of a single charge transfer controlled cathodic reaction and single charge transfer controlled anodic electrochemical reaction. p and p, are Tafel slopes. [Pg.108]

To illustrate these results we have to specify the dependence R T). Typically, R is determined by one (or a combination) of the following factors (i) the resistivity of the electrolyte, (ii) the resistivity of the oxide layer covering the BP surface, and (iii) the resistivity corresponding to the activation of the anode electrochemical reaction (Section 4.6). [Pg.207]

In the previous section, we discussed fuel cell thermodynamics. However, in reality, fuel cell operation with an external load is much more practical than in a thermodynamic state. When a H2/air PEM fuel cell outputs power, the half-electrochemical reactions will proceed simultaneously on both the anode and the cathode. The anode electrochemical reaction expressed by Reaction (l.I) will proceed from H2 to protons and electrons, while the oxygen from the air will be reduced at the cathode to water, as expressed by electrochemical Reaction (l.II). For these two reactions, although the hydrogen oxidation reaction (HOR) is much faster than the oxygen reduction reaction (ORR), both have limited reaction rates. Therefore, the kinetics of both the HOR and the ORR must be discussed to achieve a better understanding of the processes occurring in a PEM fuel cell. [Pg.14]

The anode electrochemical reaction of a H2/O2 PEM fuel cell can be expressed using Reaction (l.I) in Chapter 1. The generally accepted mechanism of the HOR on a Pt catalyst includes three steps [9,17,21-23] (1) the adsorption of H2 on the Pt surface, (2) the dissociated chemical adsorption of the adsorbed H2, which is considered the rate-determining step of the HOR, and (3) the fast electrochemical oxidation of adsorbed hydrogen atoms, producing protons. These three steps are expressed in Reactions (l.IV), (l.V), and (l.VI), respectively, whereas the electrode kinetics of the HOR has been addressed in Section 1.3.1 of Chapter 1. [Pg.129]

The Mg " is directly anodized into Mg via an anodic electrochemical reaction ... [Pg.26]

It is proposed to develop a fuel cell that runs directly on propane (CsHg g) at a propane stoichiometry (XCsHg) of 2.5 and a cathode oxygen stoichiometry (A.,) of 2 (note the cathode is running on air, 79% N2, 21% O2 by volume). In the laboratory, the cell operates at 0.3 V at a current density of 0.1 A/cm. The superficial active area of the cell is 25 cm. The anode electrochemical reaction is... [Pg.118]

Electrodialysis was proposed by Bodamer [30] for the production of free ethylenediamine from an aqueous solution of its hydrochloride. A 40% solution of ethylenediamine hydrochloride was placed in the cathode compartment which was separated from the anode compartment by an anion-exchange membrane made from Amberlite IRA-400 (70%) and polyethylene (30%). A diagram of the electrodialyzer is shown in Fig. 6. The anolyte was a 0.1 N sulfuric acid solution, and the electrodes were platinum. The products from the cathodic and anodic electrochemical reactions were hydrogen and oxygen respectively. [Pg.297]


See other pages where Anode, electrochemical reactions is mentioned: [Pg.150]    [Pg.219]    [Pg.201]    [Pg.78]    [Pg.516]    [Pg.37]    [Pg.197]    [Pg.223]    [Pg.688]    [Pg.96]    [Pg.148]    [Pg.196]    [Pg.247]    [Pg.9]    [Pg.272]    [Pg.59]    [Pg.60]    [Pg.249]   


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Anode reactions

Anodic electrochemical reactions

Anodic electrochemical reactions

Anodic reactions

Electrochemical anodization

Electrochemical corrosion anodic partial reaction

Electrochemical deposition anodic reaction

Electrochemical reactions

First anodic electrochemical reaction

Second anodic electrochemical reaction

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