Alloying elements, effect cobalt

The important (3-stabilizing alloying elements are the bcc elements vanadium, molybdenum, tantalum, and niobium of the P-isomorphous type and manganese, iron, chromium, cobalt, nickel, copper, and siUcon of the P-eutectoid type. The P eutectoid elements, arranged in order of increasing tendency to form compounds, are shown in Table 7. The elements copper, siUcon, nickel, and cobalt are termed active eutectoid formers because of a rapid decomposition of P to a and a compound. The other elements in Table 7 are sluggish in their eutectoid reactions and thus it is possible to avoid compound formation by careful control of heat treatment and composition. The relative P-stabilizing effects of these elements can be expressed in the form of a molybdenum equivalency. Mo (29) ... 

Mechanical properties depend on the alloying elements. Addition of carbon to the cobalt base metal is the most effective. The carbon forms various carbide phases with the cobalt and the other alloying elements (see Carbides). The presence of carbide particles is controlled in part by such alloying elements such as chromium, nickel, titanium, manganese, tungsten, and molybdenum that are added during melting. The distribution of the carbide particles is controlled by heat treatment of the solidified alloy. 

The corrosion behaviour of amorphous alloys has received particular attention since the extraordinarily high corrosion resistance of amorphous iron-chromium-metalloid alloys was reported. The majority of amorphous ferrous alloys contain large amounts of metalloids. The corrosion rate of amorphous iron-metalloid alloys decreases with the addition of most second metallic elements such as titanium, zirconium, vanadium, niobium, tantalum, chromium, molybdenum, tungsten, cobalt, nickel, copper, ruthenium, rhodium, palladium, iridium and platinum . The addition of chromium is particularly effective. For instance amorphous Fe-8Cr-13P-7C alloy passivates spontaneously even in 2 N HCl at ambient temperature ". (The number denoting the concentration of an alloy element in the amorphous alloy formulae is the atomic percent unless otherwise stated.)... 

Recent research on more coercive media with a low noise ratio involved addition of Zn to the Co alloy system [76-79]. Addition of Zn to the cobalt alloy very effectively produces a film with a fine particle structure, which results from codeposition of elements which are hardly soluble in the matrix. Such codeposition causes segregation and hence produces a film microstructure consisting of fine particles. The fine particulate structure lowers the noise ratio and increases the coercivity of the medium. 

Cobalt occurs in two atomic forms a low temperature stable hexagonal close packed (hep) form and a high temperature stable face centered cubic (fee) form. The transformation temperature of pure cobalt is 417°C. Alloying elements such as nickel, iron, and carbon (within its soluble range) are known as fee stabilizers, and suppress the transformation temperature. Chromium, molybdenum, and tungsten, on the other hand, are hep stabilizers and have the opposite effect. 

Figure 2.16 shows the charge-discharge cycle characteristics of alloys in which part of the nickel component was replaced with cobalt. Misch metal (Mm), which is a mixture of rare earth elements such as lanthanum, cerium, praseodymium, and neodymium, was used in place of lanthanum. It was found that the partial replacement of nickel with cobalt and the substitution of the lanthanum content with Mm was very useful in improving the charge-discharge cycle life. However, such alloys have insufficient capacity, as shown in Figure 2.17 [18]. From study of the effect that their compositions had on the charge-discharge capacity, it was concluded that the best alloy elements were Mm(Ni-Co-Al-Mn)This alloy led to the commercialization of sealed nickel-M H batteries. All the battery manufacturers who use a rare earth-nickel-type alloy for the negative electrode material employ similar alloys with slightly different compositions.

Amorphous Fe-3Cr-13P-7C alloys containing 2 at% molybdenum, tungsten or other metallic elements are passivated by anodic polarisation in 1 N HCl at ambient temperature". Chromium addition is also effective in improving the corrosion resistance of amorphous cobalt-metalloid and nickel-metalloid alloys (Fig. 3.67). The combined addition of chromium and molybdenum is further effective. Some amorphous Fe-Cr-Mo-metalloid alloys passivate spontaneously even in 12 N HCl at 60° C. Critical concentrations of chromium and molybdenum necessary for spontaneous passivation of amorphous Fe-Cr-Mo-13P-7C and Fe-Cr-Mo-18C alloys in hydrochloric acids of various concentrations and different temperatures are shown in Fig. 3.68 ... 

The aforementioned fact is also the basis for the separation of co-occurring metals from each other. Whenever feasible, such electrochemical separation is an interesting and effective technique, in principle. In practice, however, such selective deposition is not considered very feasible, particularly for elements which are close neighbors in the electrochemical series. For example, the decomposition potentials of nickel and of cobalt are -0.25 V and -0.27 V, respectively. This small 0.02 V difference makes the selective deposition of nickel, leaving cobalt in the solution, or vice versa, rather difficult to achieve in practice. On the other hand, it is quite easy to co-deposit nickel and cobalt and to obtain an alloy. 

Important is the use of light rare earth elonents for production of hard magnetic materials. Most prominent are alloys of samarium with cobalt in the atomic ratio 1 5 or 2 17. It may also be assumed that in further development of these materials on a larger scale that praseodymium, neodymium, lanthanum and also individual heavy rare ecu h elements will be used to achieve particular effects. Interesting is the development of magnetic bubble memories based on gadolinium-galliiimrgarnets. 

Fig. 2. The rare-earth elements now used in rare earth-cobalt permanent magnets, their effect on magnet properties (referenced to Sm alloy), and relative cost of the rare earth component.

Corrosion of Magnesium in Neutral and Alkaline Solutions Magnesium is highly susceptible to galvanic corrosion. Small amounts of impurities in the alloy can have a tremendous influence on the corrosion susceptibility. In Fig. 30, the influence of various elements is demonstrated. Small additions of copper, iron, nickel, and cobalt have an extremely negative effect on the corrosion resistance. The tolerance Kmit for iron is 0.015%, for nickel 0.0005%, and for copper 0.1% [35]. Because of the low solid solubility of these elements, they precipitate as inclusions. These act as active cathodic sites for the... 

Schmitt [52] reviewed the effect of elemental sulfur on corrosion of construction materials (carbon steels, ferric steels, austenitic steels, ferritic-austenitic steels (duplex steels), nickel and cobalt-based alloys and titanium. Wet elemental sulfur in contact with iron is aggressive and can result in the formation of iron sulfides or in stress corrosion cracking. Iron sulfides containing elemental sulfur initiate corrosion only when the elemental sulfur is in direct contact with the sulfide-covered metal. Iron sulfides are highly electron conductive and serve to transport electrons from the metal to the elemental sulfur. The coexistence of hydrogen sulfide and elemental sulfur in aqueous systems, that is, sour gases and oils, causes crevice corrosion rates of... 

Only in recent years have such universal analytical solutions been developed for XRF analysis. Even if there is still a large development potential for the future to be found in these programs, for example the precalibrated MetalQuant program for effective quantitative XRF analysis of different elements in iron, copper, nickel, cobalt and aluminum based alloys, most users already appreciate them. 

The usual alloying additions to aluminum in order to improve physical properties include Cu, Si, Mg, Zn, and Mn. Of these, manganese may actually improve the corrosion resistance of wrought and cast alloys. One reason is that the compound MnAle forms and takes iron into solid solution. The compound (MnFe)Alg settles to the bottom of the melt, in this way reducing the harmful influence on corrosion of small quantities of alloyed iron present as an impurity [27]. No such incorporation occurs in the case of cobalt, copper, and nickel, so that manganese additions would not be expected to counteract the harmful effects of these elements on corrosion behavior. 

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