Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Cathodic reduction reaction

Electrochemical reductions of sulphones have been reviewed212, and have been discussed at intervals213-215. There is evidence that the cathodic reduction reaction proceeds via a radical anion, followed by a cleavage reaction, as outlined in equation (91)212,213. [Pg.962]

If the sign of the standard reduction potential, E°, of a half-reaction is positive, the half-reaction is the cathodic (reduction) reaction when connected to the standard hydrogen electrode (SHE). Half-reactions with more positive E° values have greater tendencies to occur in the forward direction. Hence, the magnitude of a halfcell potential measures the spontaneity of the forward reaction. [Pg.358]

Currently, the most widely applied electrolyte in PEFCs is Nation, manufactured by DuPont, Dow Chemical, Midland, MI, USA and other chemical companies. The Nation polymer electrolyte is a good proton conductor. Besides, it has very low electron conductivity, and is gas impermeable in order to provide the necessary spatial separation between the anode oxidation and the cathode reduction reactions. [Pg.412]

Devise a cathodic reduction reaction to occur during discharge of a cell that would reduce Oj in the melt and be comparable with the A1 organic type of solution. [Pg.767]

The symmetry factor P in Eq. 5D is discussed in Section 12.4. Equations 4D and 5D are applicable to anodic (oxidation) reactions, for which changing the potential in the positive direction shifts the equilibrium toward the products and increases the reaction rate. For cathodic (reduction) reactions, a positive sign should be used in both equations. When Eq. 5D is substituted into the rate equation we have... [Pg.67]

For etching at the OCP where the amount of anodic dissolution equals that of cathodic reduction, reactions (6.3), (6.6), (6.8), and (6.9) operate at high HF/CrOs ratios whereas reactions (6.4) to (6.9) are involved at low HF/CrOs ratios. [Pg.256]

The cathodic reduction reaction (5.2b) increases the pH value of the solution at the cathode-electrolyte interface and gives rise to acid-base reactions. [Pg.147]

The cathodic reduction reactions commonly observed are the hydrogen evolution reactions ... [Pg.778]

Anode (oxidation) reaction Zn(s) Cathode (reduction) reaction -I- 2e ... [Pg.923]

As described above, corrosion involves at least one anodic oxidation reaction that liberates electrons, and at least one cathodic reduction reaction that consumes the electrons. The anodic and cathodic sites must be electrically connected, and an electronic current flows between these sites through the metal. The circuit is completed by a current that flows in the electrolyte between the anodic and cathodic sites. Current flows in electrolytes... [Pg.6]

The analogies which exist between anodic oxidation and cathodic reduction reactions of aromatic compounds are extensive radicals formed from radical cations by chemical reaction can be further oxidised by other radical cations, i.e. by an overall disproportionation mechanism. Thus the formation of trans 9,10-dihydroxy 9,10-diphenyl anthracene on the addition of water to a solution of 9,10-diphenyl anthracene... [Pg.762]

Acid solutions (low pH) are more corrosive than neutral or alkaline solutions. In ordinary iron or steel, the dividing line between rapid corrosion in acid solution and moderate or low corrosion is nearly neutral or alkaline solution at pH 7.5. In case of corrosion of iron or steel in aerated water, anodic reaction takes place at all pH values as per Eq. (1.1), but the corrosion rate varies due to changes in the cathodic reduction reaction as per Eq. (1.2). In the intermediate pH 4-10 ranges, loose, porous, ferrous oxide deposit shelters the surface and maintains the pH at about 9.5 beneath the deposit. The corrosion rate is nearly constant and is determined by uniform diffusion of dissolved oxygen through deposit in this range of pH. In more acidic solutions ([Pg.11]

From an engineering standpoint, the kinetics or rate of corrosion of a system is usually of primary importance. Corroding systems are not in equilibrium and therefore thermodynamic calculations cannot be applied. For metal corrosion to occur, an oxidation reaction (generally metal dissolution or oxide formation) and a cathodic reduction reaction (such as oxygen reduction) proceed simultaneously. In most normal water environments, the overall reaction for aluminium corrosion is reaction with water to form aluminium hydroxide and hydrogen. The aluminium hydroxide has very low solubility in water and precipitates as bayerite or boehmite, depending on the temperature of the water [2.8]. [Pg.37]

When dealing with the problem of the electronic work function at the metal-solution interface, one should also consider the possible role of formation of solvated electrons as intermediate products of cathodic reduction reactions. The hypothesis according to which this step is practically universal for a cathodic process was advanced in recent years by a number of investigators. Their reasoning, however, is not convincing, as was first shown by Conway neither the kinetic pattern nor the relations between thermodynamic parameters correspond, for the usual interval of potentials, to such a mechanism (this discussion is summarized in Refs. 38, 39 and 45). Walker s attempt " to demonstrate, with the aid of optical measurements, the appearance of solvated electrons in the cathode layer was also refuted. [Pg.105]

During cell overcharge, a part of the irreversible energy 7a F and - t7c 1 rn y be used to overcome the activation energy of anode and cathode degradation, respectively, and of electrolyte anodic oxidation and cathodic reduction reactions, which account for cell selfdischarge and aging [11,21-24],... [Pg.573]


See other pages where Cathodic reduction reaction is mentioned: [Pg.696]    [Pg.18]    [Pg.231]    [Pg.417]    [Pg.38]    [Pg.829]    [Pg.26]    [Pg.329]    [Pg.178]    [Pg.115]    [Pg.479]    [Pg.123]    [Pg.2184]    [Pg.829]    [Pg.38]    [Pg.2694]    [Pg.234]    [Pg.205]    [Pg.1740]    [Pg.1783]    [Pg.1808]    [Pg.315]    [Pg.275]    [Pg.2671]    [Pg.2433]    [Pg.6974]    [Pg.5]    [Pg.1047]    [Pg.168]    [Pg.117]    [Pg.219]    [Pg.221]   
See also in sourсe #XX -- [ Pg.5 ]




SEARCH



Cathode oxygen reduction reaction

Cathode reaction

Cathode reduction

Cathodic oxygen reduction reaction

Cathodic reactions

Cathodic reduction

Cathodic-reactant reduction reaction

Oxygen reduction reaction cathode electrocatalysts

© 2024 chempedia.info