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Potential galvanic

In galvanic coupling, titanium is usually the cathode metal and consequently not attacked. The galvanic potential in flowing seawater in relation to other metals is shown in Table 10. Because titanium is a cathode metal, hydrogen absorption may be of concern, as it occurs with titanium complexed to iron (38). [Pg.104]

Generai description. Galvanic corrosion refers to the preferential corrosion of the more reactive member of a two-metal pair when the metals are in electrical contact in the presence of a conductive fluid (see Chap. 16, Galvanic Corrosion ). The corrosion potential difference, the magnitude of which depends on the metal-pair combination and the nature of the fluid, drives a corrosion reaction that simultaneously causes the less-noble pair member to corrode and the more-noble pair member to become even more noble. The galvanic series for various metals in sea water is shown in Chap. 16, Table 16.1. Galvanic potentials may vary with temperature, time, flow velocity, and composition of the fluid. [Pg.328]

An electrochemical interaction of two or more materials (materials 1 and 2 in Fig. 16.1) having a sufficiently distinct galvanic potential difference... [Pg.356]

In simple terms, galvanic potential is related to the magnitude of the current induced by coupling dissimilar materials exposed to a common conductive fluid. The magnitude of the potential depends on the materials that are coupled and on the characteristics of the fluid to which the metals are exposed. [Pg.359]

A galvanic series has been constructed that lists numerous industrial metals according to their galvanic potential in sea water. Table 16.1 is such a listing for metals often found in cooling water systems. [Pg.359]

Consideration of the basic elements characteristic of the galvanic corrosion process, as discussed above, points to the principles of sound preventive techniques. Since a galvanic potential difference is the driving force for corrosion reducing the magnitude of this difference can reduce or prevent galvanic corrosion. [Pg.363]

When possible, avoid coupling materials having widely dissimilar galvanic potentials. If this cannot he avoided, make use of favorable area ratios by giving the active metal a large exposed area relative to the noble metal. For example, copper or copper-based alloy tubes may be joined to a steel tube sheet. Because of the favorable area ratio in this case, a relatively inexpensive steel tube sheet may be intentionally substituted for a bronze or a brass tube sheet if thickness specifications allow for a small amount of galvanic corrosion of the steel. [Pg.364]

The galvanic potential of metals can vary in response to environmental changes such as changes in fluid chemistry, fluid-flow rate, and fluid temperature. For example, at ambient temperatures steel is noble to zinc (as in galvanized steel). In waters of certain chemistries, however, a potential reversal may occur at temperatures above 140°F (60°C), and the zinc becomes noble to the steel. [Pg.366]

Scales of Galvanic Potentials are useful indicators of galvanic corrosion however, information is needed on the amount of current flowing between dissimilar metals. [Pg.38]

The galvanic potential E is related to the difference in chemical potential by the relation ... [Pg.1307]

Air is normally the reference gas used in the exhaust gas sensor. If the oxygen partial pressure in the engine exhaust gas is known as a function of the engine air/fuel ratio, the theoretical galvanic potential of the sensor is easily determined by the Nernst equation. [Pg.1308]

Thus, the temperature coefficient of Galvanic potential of an individual electrode can be neither measured nor calculated. Measured values of the temperature coefficients of electrode potentials depend on the reference electrode employed. For this reason a special scale is used for the temperature coefficients of electrode potential It is assumed as a convention that the temperature coefficient of potential of the standard hydrogen electrode is zero in other words, it is assumed that the value of Hj) is zero at all temperatures. By measuring the EMF under isothermal conditions we actually compare the temperature coefficient of potential of other electrodes with that of the standard hydrogen electrode. [Pg.52]

Liquid-solid contact Liquid-liquid contact Statistical distribution due to ion concentration fluctuations Double layer (zeta potential) disruption Volta potential (for electron conducting materials) Electrolytic (galvanic) potential (for ionic systems)... [Pg.56]

Let us now consider a galvanic cell with the redox couples of equation 8.164. This cell may be composed of a Cu electrode immersed in a one-molal solution of CUSO4 and a Zn electrode immersed in a one-molal solution of ZnS04 ( Dan-iell cell or Daniell element ). Equation 8.170 shows that the galvanic potential is positive the AG of the reaction is negative and the reaction proceeds toward the right. If we short-circuit the cell to annul the potential, we observe dissolution of the Zn electrode and deposition of metallic Cu at the opposite electrode. The flow of electrons is from left to right thus, the Zn electrode is the anode (metallic Zn is oxidized to Zn cf eq. 8.167), and the Cu electrode is the cathode (Cu ions are reduced to metallic Cu eq. 8.168) ... [Pg.543]

Uhlig was thermodynamically oriented and for him corrosion occurred because of the difference in the Galvanic potentials of the components making up a corroding surface. He believed that corrosion originated from the presence of inclusions, detected or not, in the corroding material. [Pg.207]

Steel-AI Salt solutions Galvanic potential and current measured 3... [Pg.545]

Galvani potential difference - potential, subentry -> galvanic potential difference... [Pg.290]

Massive electrochemical attack known as galvanic corrosion [58,59] is the most severe form of copper corrosion. It can completely remove the copper from the structures (Figs. 17.25 and 17.26). It can occur when the wafers are exposed to a corrosive electrolyte for an extended period. It can also occur if the slurry does not contain enough or effective corrosion inhibitor. The source of such a galvanic potential on the patterned copper surface may be due to the fact that some copper structures connected to transistors have a different electrical potential than the rest of the wafer surface. Another possible cause of this type of galvanic potential is related to the barrier material induced metal metal battery effect. Most copper CMP slurries have been developed for Cu structures with Ta or TaN as a barrier material. In some cases, other metals may also be used in addition to the barrier metal. For example, a metal hard mask could contribute to the galvanic corrosion effects. It is also possible that some types of copper are more susceptible to corrosion that others. The grain... [Pg.534]

The estimations of galvanic potentials and current densities were confirmed by experimental measurements shown in Figure 6. In the TMAH solution, the measured galvanic current density is 20 nA/cm and the potential is 0.125 V. In NH4OH, the current density is 30 nA/cm and the potential is 0.15 V. These values agree well with values estimated from the polarizations shown in Figures 4 and 5. [Pg.165]

Figure 4 - The influence of agitation speed on the galvanic potential (a) and current (b) between gold (Au) and roasted gold ore (RGO) electrodes, pH 10.5,25 °C, cyanide cone. 0.01 M, 25 °C, saturated atmospheric oxygen, Au electrode surface area 0.25 cm2, RGO area 4.9 cm2... Figure 4 - The influence of agitation speed on the galvanic potential (a) and current (b) between gold (Au) and roasted gold ore (RGO) electrodes, pH 10.5,25 °C, cyanide cone. 0.01 M, 25 °C, saturated atmospheric oxygen, Au electrode surface area 0.25 cm2, RGO area 4.9 cm2...

See other pages where Potential galvanic is mentioned: [Pg.563]    [Pg.22]    [Pg.359]    [Pg.364]    [Pg.397]    [Pg.11]    [Pg.135]    [Pg.837]    [Pg.140]    [Pg.190]    [Pg.194]    [Pg.938]    [Pg.99]    [Pg.81]    [Pg.259]    [Pg.346]    [Pg.544]    [Pg.164]    [Pg.70]    [Pg.6]    [Pg.8]    [Pg.9]   
See also in sourсe #XX -- [ Pg.216 ]

See also in sourсe #XX -- [ Pg.216 ]




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