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Industrial electrolysis voltage

O Most industrial reactions take place on a much larger scale than reactions in a laboratory or classroom. The voltage used in a Downs cell for the industrial electrolysis of molten sodium chloride is not very high, about 7 V to 8 V. However, the current used is 25 000 A to 40 000 A. Assuming a current of 3.0 x 10 A, determine the mass of sodium and the mass of chlorine made in 24 h in one Downs cell. Express your answers in kilograms. [Pg.545]

Diffusion overpotential — The diffusion overpotential means the extra voltage which could compensate the difference between bulk concentration and surface concentration, and is called -> concentration overpotential [i]. As a performance of industrial electrolysis or batteries, it has been used along with -> activation overpotential and - ohmic overpotential. It not only varies compli-catedly with cell configuration, current, applied voltage, and electrolysis time but also cannot be separated from activation and ohmic overpotentials. [Pg.156]

One important technical evaluation criterion for electrolytic processes is the efficiency, i.e. the cost-benefit ratio for an industrial electrolysis system. When determining the efficiency, it is expedient to utilize the heating value (3.54 kWh Nm ) or the thermoneutral voltage Vth = 1.48 V because in commercial electrolysis systems for alkaline and PEM electrolysis, water is added in its liquid state. As such, the efficiency referring to the heating value of hydrogen specifies how efficiently the electrolyzer or the entire electrolysis system with all auxiliary components can be operated. [Pg.193]

In the absence of any specific properties (which is wholly opposite to the case of selective membranes) these effective parameters can sometimes be related to microscopic parameters, such as the porosity and tortuosity in the materials used. Assuming that the membrane is not ion-selective with respect to the different ions, one can consider the transport numbers to be constant in all the electrolytic media. In the examples outlined below (see sections 4.4.2.2 and 4.4.2.3), it is assumed that the effective diffusion coefficients and mobilities are significantly lower than in the free electrolyte. This is due for exampie to a low porosity in the material used. Note that if these particular experimental conditions are chosen, then it implies that there is a significant ohmic drop in the eiectroiysis cell, which requires high electrolysis voltages (typically over 10 V). These conditions are not suitable for industrial applications. [Pg.250]

Encouraging laboratory experiments since 1994 with oxygen-depolarised cathodes (ODC) in chlor-alkali as well as hydrochloric acid electrolysis motivated the development of this technique up to the industrial scale. Based on the predictions of the theory, the reduction of cell voltage could be expected up to 1 V (Fig. 4.1) for both applications. Early on, the proper choice and improvement of ODC, deriving mainly from the DeNora group, led to results with voltages as predicted in short tests as well as in endurance tests conducted over dozens of months at the Bayer endurance test facilities. [Pg.63]

Zinc electrolysis consumes a large amount of electric power (>3000kWht 1 Zn), with a cell voltage higher than 3 V. Usually, the current density is about 500 Am-2, but values ranging from 300 to 750 Am-2 are found in normal industrial activity, with current efficiencies of 90-93%. [Pg.722]

Ando and Tanaka have recently used a Naflon electrolyte in electrolysis mode to decompose two water molecules to simultaneously generate one molecule of hydrogen and one of hydrogen peroxide (used in paper/pulp and chemical industries). They do this by using a high applied voltage (1.77 to 2.00 V) in a two-electron... [Pg.42]

Electrochemical reactions can also be driven by external voltage sources in a process called electrolysis. Electrolysis has important industrial appUcations for coating materials with metals. The amount of material in a coating can be determined accurately through a stoichiometric calculation in which the current and time tell us the number of electrons involved in the process. [Pg.568]

First electrochemical production of adiponitrilehad developed by Monsanto in 1963 and commercialized in 1965. Monsanto process adopted a homogeneous electrolysis system. On the other hand, Asahi Chemical Industry (presently Asahi Kasei Chemicals) started the commercial adiponitrUeplant withan emulsion electrolysis system in 1971. Both of the processes were operated in the divided cell equipped with separator such as ion exchange membrane in the first stage of development and have improved into operation in undivided cell in order to reduce higher cell voltage caused by resistance of separator. [Pg.153]

Electrochemical oxidation and reduction of het-ero atom compounds, such as N, S, and P compounds, has been intensively studied and utilized for synthesis of many fine chemicals [1-4]. Electrooxidative S-S, S-N, S-P, and N-P bond formation is performed successfully by electrolysis of thiols, disulfide/amine, disulfide/phosphate, amine/ phosphate, and so on, affording useful chemicals, e.g., thiuram disulfide [17], sulfenamide [18], sulfenimides [19], phosphorothiolates [20], phosphoramidate [21], and so on. For instance, cross-coupling of phthalimide and dicyclohexy disulfide is performed by electrolysis in acetonitrile containing a catalytic amount of sodium bromide under a ccaistant apphed voltage (3 V, 0.7-0.9 V vs. SCE) to afford N-(cyclohexylthio)phthalimide, an important prevulcanization inhibitor in the rubber industry, in quantitative yield [19] (Fig. 4). [Pg.805]

Electrolysis is employed industrially to isolate elements from their ores. In some cases, a product (usually a gas) may form so slowly (high activation energy) that a higher-than-expected voltage (overvoltage) must be applied. (Section 21.7)... [Pg.687]

The industrial preparation of hydrogen by the electrolysis of water on nickel electrodes requires a voltage of more than 1.50 V (1.23 V + 0.210 V + 0.060 V) since it is necessary to add the RI drop (due to the internal resistance of the electrolyte). However, at very high current densities, the polarization is much higher, and higher temperatures are used to reduce the excess power... [Pg.148]


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See also in sourсe #XX -- [ Pg.789 , Pg.790 ]




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