Salt solutions nickel-iron alloys

Nickel-iron alloys are more resistant than iron to attack by solutions of various salts. In alternate immersion tests in 5% sodium chloride solution Fink and De Croly determined values of 2-8, 0-25 and 0-5 g m d for alloys containing 37, 80 and 100% nickel compared with 46 g m d for iron. Corrosion rates of about 0.4 g m d are reported by Hatfield for Fe-30Ni alloy exposed to solutions containing respectively 5 Vo magnesium sulphate, 10 Vo magnesium chloride and 10% sodium sulphate the same alloy corroded at a rate of about 1.2 g m d in 5% ammonium chloride. 

Nickel is used throughout industry because of its excellent corrosion resistance. In addition to itr+us37- oe/oe" nn< cladding material to provide corrosion resistance to tanks and production vessel surfaces, nickel is used as an alloying element in steel production. Nickel is resistant to attack by NaOH and other alkali solutions, but is not compatible with ammonium hydroxide. Nickel is resistant to corrosion by sodium chloride solutions, but is corroded severely by iron, copper- and mercury chloride salts. Also, nickel has excellent corrosion resistance to most organic acids. Some of the common nickel alloys are described below ... 

Zirconium alloys generally have good corrosion resistance in salt solutions and are relatively insensitive to iron and nickel. When magnesium is alloyed with zirconium, most of the iron is present as insoluble particles in combination with zirconium (Chapter XX in Emley, 1966). As a consequence, the iron contaminant is precipitated from the alloys before casting. All zirconium-grain-refined alloys are high purity in iron, and to a lesser extent nickel, because these impurities are naturally controlled to very low levels by precipitation with zirconium (Tawil, 1990). 

In atomization, a stream of molten metal is stmck with air or water jets. The particles formed are collected, sieved, and aimealed. This is the most common commercial method in use for all powders. Reduction of iron oxides or other compounds in soHd or gaseous media gives sponge iron or hydrogen-reduced mill scale. Decomposition of Hquid or gaseous metal carbonyls (qv) (iron or nickel) yields a fine powder (see Nickel and nickel alloys). Electrolytic deposition from molten salts or solutions either gives powder direcdy, or an adherent mass that has to be mechanically comminuted. 

Electroplated Metals and Alloys. The metals electroplated on a commercial scale from specially formulated aqueous solutions iaclude cadmium, chromium, cobalt, copper, gold, iadium, iron, lead, nickel, platinum-group metals, silver, tin, and ziac. Although it is possible to electroplate some metals, such as aluminum, from nonaqueous solutions as well as some from molten salt baths, these processes appear to have achieved Httie commercial significance. 

Fe, Ti, Ni, and Cu in ball or vibrational mills particles are obtained in the form of irregular polyhedra on milling such alloys as Fe—Al, Al—Ni—Co, and Al—Si—Fe in vortical mills, the particles have a plate-like shape. On the condensation of nickel and iron carbonyls spherical particles are formed in the reduction of metals (W, Mo, Fe, Ni, Co, Cu, Pt, Sn, Ag, Au, etc.) from their salts or oxides, and also on electrolysis of salt melts or solutions, the metal particles produced have the shape of dendrites. 

Galvanic corrosion or bimetallic corrosion is important to consider since most of the structural industrial metals and even the metallic phases in the microstructure alloys create galvanic cells between them and/or the a Mg anodic phase. However, these secondary particles which are noble to the Mg matrix, can in certain circumstances enrich the corrosion product or the passive layer, leading to a decrease or a control of the corrosion rate. Severe corrosion may occur in neutral solutions of salts of heavy metals, such as copper, iron and nickel. The heavy metal, the heavy metal basic salts or both plate out to form active cathodes on the anodic magnesium surface. Small amounts of dissolved salts of alkali or alkaline-earth metal (chlorides, bromides, iodides and sulfates) in water will break the protective film locally and usually lead to pitting (Froats et al., 1987 Shaw and Wolfe, 2005). 

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