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Electrodes basic

The properties of the basic electrodes also mean much better impact properties at low temperatures. [Pg.19]

The disadvantage with basic electrodes welded vertically up is the low current that has to be used resulting in low productivity. [Pg.19]

This can be avoided by using basic electrodes developed specially for welding of pipelines in the vertical-down position. These electrodes contain iron powder in the coating and therefore have higher productivity than cellulose electrodes since they also can be welded at higher currents than cellulose electrodes. [Pg.19]

Productivity is 25-30% higher than for cellulose electrodes and 40-50% higher than for basic electrodes in vertically up welding. [Pg.19]

In the root, the penetration and force from a cellulose electrode is however the most productive process since they can manage a small root-opening with high current resulting in fast progression. A basic electrode can be used also for the root but requirements on alignment will be higher because of the less forceful arc. [Pg.19]


In the electrolysis zone, the electrochemical reactions take place. Two basic electrode configurations are used (/) monopolar cells where the same cell voltage is appHed to all anode/cathode combinations and (2) bipolar cells where the same current passes through all electrodes (Eig. 4). To minimize the anodic oxidation of OCL , the solution must be quickly moved out of this zone to a reaction zone. Because the reaction to convert OCk to CIO (eq. [Pg.497]

The basic electrodic equation also conceals a geographic problem. The whole analysis has proceeded from the statement that the electron acceptors and donors are positioned near the electrode before being involved in the charge-transfer reaction. Where Does it matter It would surely be expected to, and very much. Both the potential and concentrations of various species can vaiy near the interface. As the location of the initial state of the reaction is altered, the potential differences and concentrations appearing in the basic equation also vaiy (see Fig. 7.9). [Pg.351]

The Basic Electrodics of Corrosion in the Absence of Oxide Films... [Pg.142]

Fig. 7.49 Basic electrode layout of the Penning gauge. From Fundamentals of Vacuum Science and Technology, by G. Lewin McGraw-Hill, New York, 1965 (Fig. 5-4), reproduced with permission. Fig. 7.49 Basic electrode layout of the Penning gauge. From Fundamentals of Vacuum Science and Technology, by G. Lewin McGraw-Hill, New York, 1965 (Fig. 5-4), reproduced with permission.
The polyethylene membrane covered an electrochemical enzymatic biosensor. The construction scheme of the sensor is displayed in Fig. 25. The electrochemical basic electrodes consist of a platinum anode and a silver-silver chloride cathode. A thermally sensitive layer of glucose oxidase was localized directly on the anode surface and was covered by a 30-pm-thick hydrophobic polyethylene membrane. The biosensor for the detection of the glucose concentration is based on an enzyme (glucose oxidase)-cat-alyzed reaction of the analyte (glucose) and the subsequent electrochemical detection of a reaction product (electron current). A stoichiometric surplus of the coreactant oxygen has to be guaranteed. This is realized by the polyethylene membrane (membrane with analyte door ) controlling the glu-... [Pg.278]

Thermal electron attachment studies in our laboratory utilize the so-called electron capture detector which is commonly used as a selective detector for gas chromatography. Our measurements are also carried out in conjunction with a gas chromatograph for reasons pointed out later. The electronic circuitry for the pulse mode of operation is identical to that originally proposed by Lovelock et al. (14,15). The electron capture cell, employing tritium as a radiative /3-source, has been modified slightly for practical reasons (22) however, the basic electrode geometry is parallel plate, as first proposed (14, 15). [Pg.79]

Some manufacturers are now supplying manual electrodes dried to very low hydrogen levels and hermetically sealed in vacuum packaging. If the packaging remains intact (and it is obvious when this is not the case), these electrodes can be used without further drying, provided they are utilised within the period stated by the manufacturer after opening, and provided the conditions of operation are within those specified by the manufacturer. Use of such electrodes is facilitated by recent improvements in the resistance of basic electrodes to pick-up of moisture, and also by the use of small packets containing only the number of electrodes which a welder is likely to use in a shift or half a shift. [Pg.8]

For medium iron powder electrodes giving electrode efficiencies above 110% and not greater than 130% (e.g. basic electrodes of AWS classes E 14 and E 18) ... [Pg.43]

It is very important to keep valve (26) in Figure 12 tightly closed during the whole elution. Otherwise the acidic or basic electrode solution will leak out of the electrode compartment. This will destroy the possibility of accurate pH measurements of the fractions which come out of the column. To prevent the leakage of electrode solution out of the central tube (19), the contents should be sucked out of the tube with the aid of a syringe and a capillary tube in order to achieve a pressure slightly under atmospheric in the tube. [Pg.43]

Electrodes of many shapes and sizes have been used and almost any shape of electrode can be made if desired. Figure 5-20 shows some of the basic electrode types and shapes. A simple cup, such as shown in Figure 5-20a, is often used for powder samples. The sample is placed in the cup and an arc struck between the cup and a counter electrode. The sample is vaporized and excited in the arc. In Figure 5-20b the cup is undercut. The temperature of the cup rises more rapidly in this case. Often the sample and cup are both volatilized into the arc. A porous cup electrode is shown in Figure 5-20c. The cup is filled with liquid and passes slowly through the porous bottom end of the electrode. An arc or spark is struck to a lower counter electrode to excite the sample. Another technique useful for liquids uses a disk electrode, as shown in Figure 5-20d. The disk rotates and feeds liquid into the arc or spark gap for excitation. Another method to introduce a liquid sample into the arc or spark is to use a cored electrode as shown in Figure 5-20e. The solution enters the electrode gap by capillary action in the core. [Pg.124]

Dielectric spectroscopy is a very promising tool to probe relaxation processes, especially since new broadband equipment can cover frequencies in the range of lO"" to 10 ° Hz. The theoretical introduction of this technique can be found in literature (Korhonen et al. 2008). Basically, electrodes of two different sizes are used, and the overall response, given by capacitance (C), depends on both the intrinsic characteristics (permittivity e) and the geometry of the sample. The relationship between capacitance and sample geometry is given by ... [Pg.532]

Figure 8 depicts the structure of the Zn-Mn02 miniature cell. It uses the same basic electrode materials as its larger cousin, the D-size alkaline cell technology. The electrode reactions are found above in Eqs. 1, 2, 3, and 4. [Pg.52]

ESs of both double-layer and battery-Uke materials such as porous carbon and RUO2, respectively, form multilayer electrode stractuies. The two electrodes either combine the two materials or use them separately. Device configuration consists of basic electrode, separator with electrolyte, and electrode design. [Pg.239]

To help with the evacuati i of the gas, it is useful to make i ysical alterations to the basic electrodes. We create slits or holes in them so as to facilitate the escape of gas bubbles. Thus, we speak of louvered electrodes, finned or slit electrodes. The design of the electrodes has evdved a great deal over the years, and is very varied. [Pg.55]

The basic electrode is an oxidation-reduction electrode operating under equilibrium conditions between electrons in a noble metal, hydrogen ions in solution, and dissolved molecular hydrogen. The activity of dissolved hydrogen, an+, is taken as the independent variable and is fixed by maintain-... [Pg.96]

The basic electrode is shown in Figure 5.7. Since calomel is relatively insoluble, KCl solution is used as the electrolyte. The electrochemical reactions which describe the half-cell are rather complex and are omitted here. The emf of the calomel electrode depends upon the concentration of the KCl solution. The following range of values can be expected ... [Pg.98]

In this case (as is the case with the basic electrodes described by Fatt), no membrane is used. The chamber into which our electrode was placed... [Pg.132]

Walker (1973) has reported a technique for producing ion-specific microelectrodes which use liquid ion exchangers. The basic electrode is shown schematically in Figure 6.15. A liquid ion exchanger is formed by an organic electrolyte dissolved in a low-dielectric-constant organic solvent. [Pg.139]

Figure 3.12 Basic electrode arrangement in electrospinning. Reprirrted with permission from Y. M. Shin et al. (2001b). Copyright 2001. Elsevier. The shaded area represents the whipping instability region. Figure 3.12 Basic electrode arrangement in electrospinning. Reprirrted with permission from Y. M. Shin et al. (2001b). Copyright 2001. Elsevier. The shaded area represents the whipping instability region.
For a long time the dropping mercury electrode was the basic electrode used in polarography. However, with time, new problems needed for their solution new electrode materials, as mercury cannot be used in the anodic range. This was the case for the direct polarographic determination of some anions, for some organic compounds, and for noble metal and rare-earth metal ions. The mercury electrode... [Pg.152]


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See also in sourсe #XX -- [ Pg.31 , Pg.43 , Pg.52 , Pg.60 , Pg.63 , Pg.71 , Pg.104 , Pg.105 ]




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