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Solutions alloys

However, it turns out that native copper is extraordinaiily variable in composition even within single sources. Native copper nonnally contains a vaiiable amount of other, nonmetallic minerals including copper sulfides, oxides, and silicates. These other minerals are not ductile but break upon cold-working the copper, which decreases the amounts of these minerals in varying amounts and thus alters the composition. Other elements that are soluble in an alloy solution with copper increase in abundance simply because the ratio of metal to nonmetal changes. [Pg.225]

The simple model fits observation remarkably well for pure metals. However, this model begins to fail for alloys (solutions of one metal in another), such as brass and bronze, where for certain stoichiometries the material has anomalous physical properties and behaves almost as a componnd (e.g., CuZn and Cu5Sn, termed Hume-Rothery electron phases). [Pg.162]

Alloy solute /kcal Alloy solute /kcal ... [Pg.75]

Spectrophotometry Flame AAS 1000 ngL- " (soil, minerals, alloys) Solution Michel (1988)... [Pg.1088]

EGBE forms explosive mixtures with air in the range 1.1-10.6% by volume of air. Comas et al. (1974) reported the hazards associated with EGBE-perchloric acid solutions used for electropolishing alloys. Solutions containing 50-95% acid constitute explosion danger at room temperature. Acid concentration up to 30% is safe in the absence of an electric spark, solvent evaporation, or heating up to the flash point, 60° C (140°F) of the solvent. [Pg.415]

Low-carbon steel, high-strength steels Austenitic stainless steels a-Brass Titanium alloys (8% Al, 1% Mo, 1% V) Aluminum alloys Solutions containing NOj, OH , H2O Solutions containing Cl , OH , Br NH3, amines Solutions containing Cl , Br , H2O, NaCl solutions... [Pg.261]

Preparation of water samples and certified metal alloy solution... [Pg.429]

The analytical value of total iron in water is in good agreement with that obtained by the AAS method. The accuracy of the proposed method was tested by the analysis of a certified metal alloy solution (MBH Zn/Al/Cu 43XZ3F). Three replicates of the solution using the sampling volume of 20 pL were analyzed. The certified and the obtained values were 0.085 % and (0.084 0.006) of iron, respectively. An excellent agreement between the found and... [Pg.432]

Maintaining the potential of the alloy-solution interface at sufficiently low potential has been shown to prevent crevice corrosion stabilization [58]. As shown in Fig. 25, the repassivation potential for crevice corrosion becomes independent of the amount of charge passed. Kehler and coworkers [59] have demonstrated the same for Alloy 625 and Alloy 22, including the deleterious effects of increased temperature and concentration ratio of [Cl ] [other anions]. Data for AUoy 22 are shown in Fig. 26. [Pg.305]

Recall that grain boundaries are sinks in which impurities or solute might become concentrated. The thermodynamic description of equilibrium segregation involves redistribution of alloyed solute such that the total free energy of the system is minimized. For a two-component system such as a binary alloy, if one considers a dilute solution of component B dissolved as solute in solvent A, the surface excess of B at surfaces per unit area, Fb, is given by [7, 9]... [Pg.351]

Tan4] Tanaka, A., Carbon Solubilities in Mn, Mn-Fe, Mn-Si and Mn-Fe-Si Alloy Solutions (in Japanese),MMroraM Kogyo Daigaku Kenkyu Hokoku, Riko Hen, 10, 19-31 (1980) (Phase Relations, Experimental, 8)... [Pg.169]

Metals don t really react with other metals to form compounds. Instead, the metals combine to form alloys, solutions of one metal in another. But there is such a situation as metallic bonding, and it s present in both alloys and pure metals. In metallic bonding, the valence electrons of each metal atom are donated to an electron pool, commonly called a sea of electrons, and are shared by all the atoms in the metal. These valence electrons are free to move throughout the sample instead of being tightly bound to an individual metal nucleus. The ability of the valence electrons to flow throughout the entire metal sample is why metals tend to be conductors of electricity and heat. [Pg.102]

Figure 6.20 Average chromium content of passive film of Fe-Cr alloys, measured with XPS, as a function of Cr concentration in the alloy. Solution is 0.5M H2SO4. The dashed curve is calculated using equation (6.13) [13,15]. Figure 6.20 Average chromium content of passive film of Fe-Cr alloys, measured with XPS, as a function of Cr concentration in the alloy. Solution is 0.5M H2SO4. The dashed curve is calculated using equation (6.13) [13,15].
Different kinds of alloys—solution alloys, heterogeneous alloys, and intermetallic compounds—are described. [Pg.919]

A mathematical explanation for the severity of the room temperature diffusion problem, exemplified by silver-gold, can be summarized as follows Data [76,77] demonstrate that interdiffusion at room temperature is too slow to account for deallo5dng. Diffusion coefficients previously vised were extrapolated from values taken above 600°C. Data taken nearer room temperature cast doubt on earlier extrapolations and allow much more reliable values for diffusion coefficients to be obtained. These values could not account for diffusion of the silver to the solution interface, which would require diffusion of many orders of magnitude faster for removal of all of the silver from the alloy. Since, in some alloy compositions at room temperature, all of the silver can be ionized and removed from the alloy within a few minutes, bulk diffusion cannot be the means for moving the silver to the surface for ionization. There must be a much faster method by which the less noble metal can reach the solution metal interface, because volume diffusion can only account for a fraction of the movement required to ionize all of the less noble metal at the alloy-solution interface. [Pg.280]

Alloy solutions were prepared by dissolving 0.2-0.5 g of the standard alloys in about 15 ml cone. HCl and 2-4 ml cone. HNO3 by heating on a water bath. The solution was evaporated nearly to dryness, another 10 ml of cone. HCl was added to it, diluted with water, filtered and made up to 50 ml in a standard volumetric flask (182). [Pg.514]

Example 3.3 Determine the atomic weight of 82Mg — lOAl — 8Zn alloy. Solution ... [Pg.79]

Mechanical-Property Data Ti-6Al-2Zr-2Sn-2Mo-2Cr Alloy Solution IVeated and Aged Plate, F33615-72-C-1280, Battelle Columbus Laboratories, Apr 1973... [Pg.366]


See other pages where Solutions alloys is mentioned: [Pg.122]    [Pg.462]    [Pg.57]    [Pg.776]    [Pg.112]    [Pg.271]    [Pg.431]    [Pg.96]    [Pg.272]    [Pg.91]    [Pg.433]    [Pg.159]    [Pg.300]    [Pg.74]    [Pg.3]    [Pg.220]    [Pg.220]    [Pg.220]    [Pg.220]    [Pg.1857]    [Pg.1990]    [Pg.495]    [Pg.1071]    [Pg.76]    [Pg.117]    [Pg.172]    [Pg.115]    [Pg.288]   
See also in sourсe #XX -- [ Pg.474 ]




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Alloy catalysts solid solutions

Alloy films solid-solution

Alloying elements solid solutions

Alloys regular solution parameters

Alloys solid solution

Aluminum alloys corrosion chloride-containing solutions

Basic solutions, magnesium alloys

Chemical Deposition of Metals and Alloys from Aqueous Solutions

Copper-zinc alloy solution

Crystalline solids alloy solid solutions

Electrodeposition of Alloys from Aqueous Solutions

Ethylene glycol solution magnesium alloys

Magnesium (Mg) alloys in ethylene glycol solution

Magnesium alloys in ethylene glycol solution

Metals alloy solid solutions

Salt solutions nickel-iron alloys

Solid-solution-type alloys

Solute redistribution in alloys

Solution-strengthened alloys

The metals and alloys (prepared utilizing liquid ammonia solutions) in catalysis II

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