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Iron anodes, sacrificial

When the technique of electroplating is used to deposit a layer of iron on another metal surface, it is usual to employ a sacrificial iron anode and a solution of a ferrous salt e. g. ferrous sulphate. (This is the usual technique for silver plating.) The typical anodic (Eqs. 6.7 and 6.8) and cathodic reactions (Eqs. 6.9-6.12) are given below. [Pg.244]

This method uses a more active metal than that in the structure to be protected, to supply the current needed to stop corrosion. Metals commonly used to protect iron as sacrificial anodes are magnesium, zinc, aluminum, and their alloys. No current has to be impressed to the system, since this acts as a galvanic pair that generates a current. The protected metal becomes the cathode, and hence it is free of corrosion. Two dissimilar metals in the same environment can lead to accelerated corrosion of the more active metal and protection of the less active one. Galvanic protection is often used in preference to impressed-current technique when the current requirements are low and the electrolyte has relatively low resistivity. It offers an advantage when there is no source of electrical power and when a completely underground system is desired. Probably, it is the most economical method for short life protection. [Pg.91]

The peroxi-coagulation method uses a sacrificial iron anode to treat a wastewater in an undivided cell containing a cathode that electrogenerates H2O2 from reaction (19.1). In this process, soluble Fe2+ is continuously supplied to the solution from the oxidation of a Fe anode as follows (Brillas et al. 1997, 1998b) ... [Pg.525]

Figure 21-13 (a) Cathodic protection of buried iron pipe. A magnesium or zinc bar is oxidized instead of the iron. The sacrificial anode eventually must be replaced. [Pg.876]

Alternatively, iron-rich sacrificial electrodes, which dissolve under acidic conditions generated at the anode by the application of electric field, may be used. The dissolved iron, in cationic form, migrates toward the cathode and then precipitates as iron-rich mineral phases (ferric iron oxyhydroxides, hematite, goethite, magnetite, and ZVl) near the cathode due to high-pH conditions. Contaminants such as Cr(Vl) can react with this iron and reduce into Cr(III). Cr(VI) transport may be limited by high sorption under low-pH conditions therefore, alkaline solution may be injected from the anode to increase the soil pH, and thereby reduce sorption and increase transport of Cr(Vl) to react with iron. [Pg.22]

Faulkner, Hopkinson, and Cundy, 2005). Because of the adverse effect of OH on soil remediation, due to the immobilization of many metal ions by precipitation in alkalinized soils, and the reduced efficiency of electrokinetic remediation when sacrificial iron-rich electrodes are employed (e.g. Leinz, Hoover, and Meier, 1998), noncorrosive electrodes and techniques to minimize soil alkalinization are generally employed for electrokinetic remediation (e.g. Rohrs, Ludwig, and Rahner, 2002 Virkutyte, Sillanpaa, and Latostenmaa, 2002). However, low adsorption of Cr(VI) in soils occurs in alkaline conditions, whereas high adsorption of Cr(VI) is favored in acidic conditions (Reddy et al, 1997). Furthermore, the reduction of Cr(VI) to Cr(III) by the delivery of iron (Fe°, Fe " ) is fairly well documented (Rai, Sass, and Moore, 1987 Eary and Rai, 1991 Haran et aL, 1995 Powell et aL, 1995 Pamukcu, Weeks, and Wittle, 1997 Batchelor et al., 1998 Reddy et /., 2003). Accordingly,under an applied direct current (DC) electric field, stabilization of Cr(VI)-contaminated soils may potentially be achieved where oxidative dissolution of iron-rich anodic electrodes provides Fe(j,q) to react with the anode-bound migration of Cr(VI). Hence, the use of iron-rich sacrificial electrodes and soil alkalinization may find application in the electrokinetic stabilization of Cr(VI)-contaminated soils. This concept is explained in this chapter based on the results of laboratory stabilization experiments on three Cr(VI)-impacted soils taken from three sites within the UK. [Pg.181]

For example, voltammetry has provided a mechanistic insight into the nickel-catalyzed homocoupling of halopyridines that results in significant improvements in the overall yield and product purity. Also, voltammetry has demonstrated the usefulness of sacrificial iron anode to produce iron ions that... [Pg.4974]

The peroxi-coagulation (PC) process, firstly proposed by BriUas group, uses an undivided cell similar to that employed for EF but containing a sacrificial iron anode instead of a stable one [1], Under such conditions, soluble Fe is released to the solution from the electrically induced dissolution of Fe by reaction (13), which follows a faradaic behavior ... [Pg.699]

In an electrocoagulation reactor, electric current is applied to a sacrificial anode and a cathode in a processing tank. Reactions at the (aluminum or iron) anode and the cathode would be a.) On an aluminum anode ... [Pg.2118]

Under the same conditions, the use of an iron anode is also necessary for the reductive dimerization of aryl halides (p-MeOPhBr, p-EtOCOPhBr, etc.). With a Mg or A1 sacrificial anode, or if electrolysis is conducted in a divided cell, aryl bromide (ArBr) is principally converted to the reduction product (ArH) [22]. [Pg.636]

The most significant chemical property of zinc is its high reduction potential. Zinc, which is above iron in the electromotive series, displaces iron ions from solution and prevents dissolution of the iron. For this reason, zinc is used extensively in coating steel, eg, by galvanizing and in zinc dust paints, and as a sacrificial anode in protecting pipelines, ship hulls, etc. [Pg.398]

As is well known, high-purity zinc corrodes much less rapidly in dilute acids than commercial purity material in the latter instance, impurities (particularly copper and iron) are exposed on the surface of the zinc to give local cathodes with low hydrogen overpotentials this result is of practical significance only in the use of zinc for sacrificial anodes in cathodic protection or for anodes in dry cells. In neutral environments, where the cathodic... [Pg.47]

It is interesting that the first large-scale application of cathodic protection by Davy was directed at protecting copper rather than steel. It is also a measure of Davy s grasp of the topic that he was able to consider the use of two techniques of cathodic protection, viz. sacrificial anodes and impressed current, and two types of sacrificial anode, viz. zinc and cast iron. [Pg.110]

Copper-base alloys will corrode in aerated conditions. It is, therefore, sometimes appropriate to consider cathodic protection. It becomes particularly relevant when the flow rates are high or when the design of an item causes the copper to be an anode in a galvanic cell (e.g. a copper alloy tube plate in a titanium-tubed heat exchanger). Corrosion can be controlled by polarisation to approximately — 0-6V (vs. CU/CUSO4) and may be achieved using soft iron sacrificial anodes. [Pg.122]

Klinghoffer, O. and Linder, B., A New High Performance Aluminium Anode Alloy with High Iron Content , Paper No. 59, Corrosion/87, San Francisco, USA, March (1987) Crundwell, R. F., Sacrificial Anodes — Old and New . In Cathodic Protection Theory and Practice, 2nd International Conference, Stratford upon Avon, June (1989)... [Pg.161]

It should be noted that when metals like zinc and aluminium are used as sacrificial anodes the anode reaction will be predominantly 10.18a and 10.186, although self-corrosion may also occur to a greater or lesser extent. Whereas the e.m.f. between magnesium, the most negative sacrificial anode, and iron is =0-7 V, the e.m.f. of power-impressed systems can range from 6 V to 50 V or more, depending on the power source employed. Thus, whereas sacrificial anodes are normally restricted to environments having a resistivity of <6 000 0 cm there is no similar limitation in the use of power-impressed systems. [Pg.202]

Foods such as meat, fish, and some vegetables contain sulfur-bearing amino acids that form volatile sulfur compounds during processing and storage. When these compounds react with iron, a black precipitate forms on the container and in most instances darkens the food. A small piece of aluminum welded to the tinplate can has been used to prevent container corrosion and sulfide staining in commercially canned hams. In this case, the aluminum acts as a sacrificial anode and stops the reaction with tin and iron that otherwise could occur at the small exposed tinplate areas (14). [Pg.48]

The chemical reactivity of metallic Mg has been utilized in several ways. It is employed in the reduction step in the manufacture of Ti, in the deoxidation and desulfurization of steels and in the nodularization of cast iron. It has also been used for the preparation of photoengraving plates, in dry batteries, and as a sacrificial anode for cathodic protection of other metals. [Pg.359]

The calculation shows that zinc is oxidized preferentially over iron. Later in this chapter we describe the use of zinc as a sacrificial anode to prevent corrosion of iron. [Pg.1387]

C19-0132. List all the metals that could be used as sacrificial anodes for iron. Which of these could also be sacrificial anodes for aluminum ... [Pg.1427]

Low-valent cobalt pyridine complexes, electrogenerated from CoCl2 in DMF containing pyridine and associated with a sacrificial zinc anode, are also able to activate aryl halides to form arylzinc halides.223 This electrocatalytic system has also been applied to the addition of aryl bromides containing an electron-withdrawing group onto activated alkenes224 and to the synthesis of 4-phenylquinoline derivatives from phenyl halides and 4-chloroquinoline.225 Since the use of iron as anode appeared necessary, the role of iron ions in the catalytic system remains to be elucidated. [Pg.486]

Halides The nickel-catalyzed cathodic addition of (Z)- or ( )-alkenylhahdes to electron-deficient olefins in the presence of a sacrificial iron rod anode proceeds with complete retention of... [Pg.434]


See other pages where Iron anodes, sacrificial is mentioned: [Pg.400]    [Pg.400]    [Pg.551]    [Pg.190]    [Pg.163]    [Pg.297]    [Pg.515]    [Pg.551]    [Pg.876]    [Pg.4030]    [Pg.129]    [Pg.130]    [Pg.50]    [Pg.278]    [Pg.1076]    [Pg.72]    [Pg.699]    [Pg.1235]    [Pg.118]    [Pg.140]    [Pg.636]    [Pg.637]    [Pg.645]    [Pg.646]    [Pg.591]    [Pg.595]    [Pg.411]   
See also in sourсe #XX -- [ Pg.848 ]




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