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Electrolysis solid

P. Choi, D. G. Bessarabov, and R. Datta, A simple model for solid polymer electrolyte (SPE) water electrolysis, Solid State Ionics, 175 535 (2004). [Pg.63]

Sridhar KR, Vaniman BT (1997) Oxygen production on Mars using solid oxide electrolysis. Solid Slate Ionics 93 321... [Pg.985]

Figure 5. Oxidative stability of ethyl docosahexaenoate in super pure water (open triangle), NaCl solution (open circle),cathodic solution just after electrolysis (solid circle) and cathodic solution after incubation for 7 days (solid triangle). (A) Decrease in unoxidized linoleate. (B) Formation of peroxides. Figure 5. Oxidative stability of ethyl docosahexaenoate in super pure water (open triangle), NaCl solution (open circle),cathodic solution just after electrolysis (solid circle) and cathodic solution after incubation for 7 days (solid triangle). (A) Decrease in unoxidized linoleate. (B) Formation of peroxides.
Kaneko Y, Mori S, Yamanaka J. Synthesis of electrochromic praseod)nnium-doped vanadium oxide films by molten salt electrolysis. Solid State Ionics. 2002 151 35-39. DOI 10.1016/SOl67-2738(02)00601-X. [Pg.109]

Graphite reacts with alkali metals, for example potassium, to form compounds which are non-stoichiometric but which all have limiting compositions (for example K C) in these, the alkaU metal atoms are intercalated between the layers of carbon atoms. In the preparation of fluorine by electrolysis of a molten fluoride with graphite electrodes the solid compound (CF) polycarbon fluoride is formed, with fluorine on each carbon atom, causing puckering of the rings. [Pg.169]

Solid Polymer E,kctroljte. The electrolyte in soHd polymer electrolyte (SPE) units is Nafion, a soHd polymer developed by Du Pont, which has sulfonic acid groups attached to the polymer backbone. Electrodes are deposited on each side of the polymer sheet. H" ions produced at the anode move across the polymer to the cathode, and produce hydrogen. The OH ions at the anode produce oxygen. These units have relatively low internal resistances and can operate at higher temperatures than conventional alkaline electrolysis units. SPE units are now offered commercially. [Pg.425]

The electrolysis is carried out at a reference potential of -2.4 volts vs a standard calomel electrode. An initial current density of 0.0403 amp/cm is obtained which drops to 0.0195 amp/cm at the end of the reduction, which is carried on over a period of 1,682 minutes at 15° to 20°C. The catholyte is filtered, the solid material is washed with water and dried. 430 g of the 2,3-bis-(3-pyridyl)-butane-2,3-diol is recrystallized from water, MP 244° to 245°C. [Pg.1013]

Sodium bicarbonate, 112-113 Sodium carbonate, 61 Sodium chloride 44q common ion effect and, 439 electrolysis, 499 formation, 3 structure, 36 Sodium chlorine, 4 Sodium hydroxide, 61,84,441 Sodium hypochlorite, 369-370 Sodium stearate, 595 Sodium vapor lamps, 135 Solids... [Pg.696]

Progress in the development of solid electrolytes is also being achieved from advances in several other fields of technology such as fuel and electrolysis cells, thermoelectric converters, electrochromic devices, and sensors for many chemical and physical quantities. [Pg.525]

Tlie anhyd salt is obtained when samples are recrystd from w above 53° below this temp a monohydrate is obtained (see below). The pure salt is best obtained on a lab scale by dissolving pure Na carbonate in a slight excess of dil aq perchloric ac, the soln partly evapd, cooled to 50°, the solid centrifuged off, and dried in a current of air at 250°. Similar results were obtained starting with pure Na chloride (Ref 2). On a coml scale it is prepd by the electrolysis of Na chlorate (see Vol 2, C197-R). Processing details and economics of the prepn are given in Refs 5 11. Coned solns are used, and modern plants use continuous electrolytic cells. In 1960 prodn was estimated to be ca 10000 tons/year at a cost of 17.56 /lb (Ref 11, p 87)... [Pg.644]

Figure 1.6. Common features of Heterogeneous Catalysis, Fuel Cell operation, Electrolysis and Electrochemical Promotion 1. Solid state catalyst, 2. Adsorption, 3. AG < 0, 4. Yield control via DC current or voltage application (Adapted from N. A. Anastasijevic). Figure 1.6. Common features of Heterogeneous Catalysis, Fuel Cell operation, Electrolysis and Electrochemical Promotion 1. Solid state catalyst, 2. Adsorption, 3. AG < 0, 4. Yield control via DC current or voltage application (Adapted from N. A. Anastasijevic).
Decarboxylation of p-lactones (see 17-27) may be regarded as a degenerate example of this reaction. Unsymmetrical diacyl peroxides RCO—OO—COR lose two molecules of CO2 when photolyzed in the solid state to give the product RR. Electrolysis was also used, but yields were lower. This is an alternative to the Kolbe reaction (11-37). See also 17-29 and 17-40. [Pg.1354]

Electrochemical processes (e.g., electrolysis, electroplating, electromachirring, crrnetrt generation, and corrosion [Plate 8]) are distinguished by their occturence in a boundary region between an electrolyte (liqtrid or solid) and an electrode. The corrrse of these processes is strongly dependent on the potential at the electrode surface, the composition and stmcture of the electrode, the composition of the electrolyte, and the microstmcture of the electrolyte in the boundary layer near the electrode surface. In certain applications, the pore size and coimectivity of the electrode can also be important. [Pg.173]

The possibility that adsorption reactions play an important role in the reduction of telluryl ions has been discussed in several works (Chap. 3 CdTe). By using various electrochemical techniques in stationary and non-stationary diffusion regimes, such as voltammetry, chronopotentiometry, and pulsed current electrolysis, Montiel-Santillan et al. [52] have shown that the electrochemical reduction of HTeOj in acid sulfate medium (pH 2) on solid tellurium electrodes, generated in situ at 25 °C, must be considered as a four-electron process preceded by a slow adsorption step of the telluryl ions the reduction mechanism was observed to depend on the applied potential, so that at high overpotentials the adsorption step was not significant for the overall process. [Pg.73]

With solid (and particularly polymeric) electrolytes which at the same time function as separators, one can appreciably reduce the distance between the electrodes and hence increase the electrode area per unit of reactor volume. Very compact equipment for water electrolysis which has no liquid electrolyte has been designed. [Pg.330]

Fuel cells (hydrogen-oxygen, hydrogen-air, methanol-air) and industrial electrolysis (water, chlor-alkali) using ion-exchange membranes are the most demanding applications for the membranes. In these apphcations, the membranes have often been designated as SPE, which can be read as solid polymer electrolyte or solid... [Pg.455]

Apart from use in metallurgical research and measurements, solid electrolytes have also been put to use as heating elements in electrical resistance furnaces. In order to prevent electrolysis from occurring, alternating currents must be used. In contrast to metallic heating elements, they may be used in air at around 2000 °C. In view of the fact that their conductivity must be very low at room temperature, there is a need for them either to be kept continuously warm, or to be preheated with an auxiliary heating element. [Pg.664]


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See also in sourсe #XX -- [ Pg.70 ]




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