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Active electrode temperature

For both low temperature electrolysers, the biggest gain in efficiency is to be expected from an improvement in Balance of Plant components, taking into account the big gap between cell efficiency (80-90%) and system efficiency (50-60%). In the case of SPE electrolysers, catalytic research should therefore be directed to making the catalysts more tolerant to contaminants. For alkaline electrolysers, in addition to this, more active electrodes could lower capital costs. [Pg.318]

In the previous section we saw how the equation of state of the adsorbed ions can be expressed as isotherms. What are the characteristics of these isotherms Isotherms, as equations of state, relate the physical quantities that define the adsoibed molecules in the electrochemical system. These physical quantities are the number of adsoibed molecules (r or 0), the activity of ions in solution (a), the charge (< M) or potential of the electrode ( ), and the temperature of the system (7). When the last two variables, qM and T, are kept constant, the mathematical expression that relates all the variables is called an isotherm. Now, if the variables that are kept constant are the activity and temperature, the name given to the equation is isoconc.56... [Pg.216]

The further improvements of the described above solution of the high-pressure alkaline electrolyser mainly concern the optimisation of the composition and preparation technology of the active electrodes. So, the application of the electrochemically-deposited materials for making the active electrodes allows to significantly reduce the voltage drop (to 0.6-1.5 V, as compared to 1.7-2.2 V which is specific value for the conventional low-temperature electrolysers). In turn, the increase of the output pressure to 200 bar makes it possible to increase the operation temperature to 150 °C that results in the reduction of the overpotential. It increases the efficiency reducing the power consumption for the production of 1 m3 H2 and 0.5 m3 02 to 4.1 kW h. [Pg.863]

Modern NMR spectrometers give access to (nearly) the whole Periodic Table, offering unmatched chemical specificity. The low-mass detection sensitivity of NMR is now less problematic, thanks to higher magnetic fields and improved electronics. In the catalytic context, NMR can work close to real-world conditions such as high pressure and high temperature, or active electrode potential control in an electrochemical environment. NMR can study both the catalytic metal itself and its adsorbates the typical pair is platinum and carbon monoxide. [Pg.477]

Figure 3.14 shows a cross-section of the novel HC sensor that consists of an oxygen pump cell and a gas-detection cell [82], In this sensor, Pt is used for the active electrode of the gas-detection cell and PrgO, is used for the inactive electrode owing to its low catalytic activity and relatively high electric conductivity. The sensing characteristics to 500 ppm of C3Hg of the proposed sensor at a temperature of 800°C are shown in Figure 3.15. The published results [82] allowed identifying... Figure 3.14 shows a cross-section of the novel HC sensor that consists of an oxygen pump cell and a gas-detection cell [82], In this sensor, Pt is used for the active electrode of the gas-detection cell and PrgO, is used for the inactive electrode owing to its low catalytic activity and relatively high electric conductivity. The sensing characteristics to 500 ppm of C3Hg of the proposed sensor at a temperature of 800°C are shown in Figure 3.15. The published results [82] allowed identifying...
Electrochemical discharges have all the characteristics of arc discharges. They occur in a very similar voltage range with similar currents and at atmospheric pressure. The question remains as to how these arcs can be initiated. We have proposed the hypothesis that the ignition is thermal [123]. The cathode temperature required is probably reached before the gas film is totally formed,3 when the active electrode bubble coverage fraction reaches its maximum value. [Pg.29]

The increase of the cathode temperature is confirmed by several studies. Guilpin [45] and Fascio [32] studied the onset of the gas film by assuming that joule heating is the mechanism of its formation. They evaluated the time required to attain, by joule heating, an electrolyte temperature of 100°C in the vicinity of the active electrode. They also measured the time needed for the formation of the gas film. Their experimental results showed that this time is similar to the time needed to heat up the electrolyte. Guilpin [45] measured the cathode temperature using thermocouples. He found typical values to be around 100°C, as did Kellogg [70] previously under similar conditions (see also Section 4.1). [Pg.29]

Note that the gas film formation time is still underestimated as at least two important effects axe neglected the heat dissipation through the active electrode (this point is discussed in more detail in the chapters on machining applications) and the heat needed for the evaporation of the electrolyte (latent heat). The conclusion to be drawn here is that this simplified model shows that in principle it is possible to build the gas film by local joule heating. Experimentally it is known that a gas film can be built around an active electrode without any gas evolution (using, for example, copper sulphate as the electrolyte and a copper electrode). It was also shown experimentally that, prior to the formation of the gas film, the electrode temperature reaches about 100°C [5,70]. [Pg.73]

Figure 4.3. Temperature increase at the active electrode as predicted by the joule heating model (4.11). (a) Computation for K = 23 (typical value corresponding to a current density of 1 A/mm2. (b) Computation for various K and for R = 106. The dashed line represents T(b) = 100°C. Figure 4.3. Temperature increase at the active electrode as predicted by the joule heating model (4.11). (a) Computation for K = 23 (typical value corresponding to a current density of 1 A/mm2. (b) Computation for various K and for R = 106. The dashed line represents T(b) = 100°C.
Different material combinations for practical realization of fuel cells have been developed in the past few decades [3] comprehensive overviews about the technology have been published [4], Possible operation temperatures of fuel cells range from ambient temperature to 1,000°C. The operation principle of the different fuel cells is depicted in Fig. 1. The main components are the same for all types of fuel cells and comprise an electrolyte, catalytically active electrodes, and a cell frame for gas distribution and current collection. Regular nanostrucmres are not typically used until now, but nanomaterials for preparation of layers are frequently the best base materials. Some examples will be given in the description of the five types of fuel cells in this introductory chapter. [Pg.153]

When the active electrode touches the tissue and the current flows directly from the electrode into the tissue without forming an arc, the rise in tissue temperature follows the bioheat equation... [Pg.298]

Corona-active electrode rotary drum handles wide range of particle diameters from 75-1000 pm high capacity < 0.75 kg/s m of drum width high efficiency 95% separates good from poor conductors. 0-40 kV DC, 0.5-1 mA/electrode insensitive to humidity and temperature often can recycle the middlings with recycling 10-30% OK. [Pg.177]


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See also in sourсe #XX -- [ Pg.80 ]




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