Copper in alloys

The zone elution method has been used for quantitative estimation or recovery of heavy metals in plants and vegetable juices [29], mercury (11) in river and waste waters [52], zinc in different environmental samples [46], nickel and copper in alloys [53], zirconium in Mg-Al alloys [22], cobalt, zinc, nickel, and copper in natural water and alloy samples [54], thiocyanate in spiked photogenic waste water [55], and aluminum in bauxite ores [42],... 

Fig. 3. Location of phases in Ni Cu alloys. ax, atomic fraction of copper in alloy x, x2, phase concentrations. From Sachtler and Jongepier (4c).

Verma and Bhuchar determined copper by reducing its tartrate complex with glucose to form insoluble CujO, which was treated with an excess of standard iodine and back-titrated with standard As(III). Oxalate was added as a complexing agent to aid in the oxidation of the CU2O, and precautions were taken to avoid air oxidation. The method has the advantage of avoiding interference from V(V). For the determination of copper in alloys, Rooney and Pratt separated copper by precipitation as its diethyldithiocarbamate from EDTA solution. 

Quantitative gas chromatographic schemes now exist for the determination of beryllium in blood, urine, and tissue,chromium in serum," aluminum in uranium, aluminum, gallium, and indium, in aqueous solu-tions," iron in ore, chromium in steel, titanium in bauxite, aluminum, iron, and copper in alloys,uranium, tungsten and molybdenum in alloys and ores, " and the list continues to grow rapidly. In the ultratrace analysis of beryllium the lower limit of detectability is ca. 10 g. The gas... 

When the melt is analyzed, the intentioned elements must be within the prescribed ranges, but not necessarily near the midpoint if the range is wide. For example, as shown in Table 19.3, copper in alloy 2024 can be skewed to a high content (sample 2) to improve strength or low content to improve toughness (sample 3). The producer will target for the nominal composition when the allowable range is only about 0.5% points or less. 

Fluorine cannot be prepared directly by chemical methods. It is prepared in the laboratory and on an industrial scale by electrolysis. Two methods are employed (a) using fused potassium hydrogen-fluoride, KHFj, ill a cell heated electrically to 520-570 K or (b) using fused electrolyte, of composition KF HF = 1 2, in a cell at 340-370 K which can be electrically or steam heated. Moissan, who first isolated fluorine in 1886, used a method very similar to (b) and it is this process which is commonly used in the laboratory and on an industrial scale today. There have been many cell designs but the cell is usually made from steel, or a copper-nickel alloy ( Monel metal). Steel or copper cathodes and specially made amorphous carbon anodes (to minimise attack by fluorine) are used. Hydrogen is formed at the cathode and fluorine at the anode, and the hydrogen fluoride content of the fused electrolyte is maintained by passing in... 

The metal looks like iron it exists in four allotropic modifications, stable over various temperature ranges. Although not easily attacked by air. it is slowly attacked by water and dissolves readily in dilute acids to give manganese(II) salts. The stable form of the metal at ordinary temperatures is hard and brittle—hence man ganese is only of value in alloys, for example in steels (ferroalloys) and with aluminium, copper and nickel. 

It is extensively used for making stainless steel and other corrosion-resistant alloys such as Invar(R), Monel(R), Inconel(R), and the Hastelloys(R). Tubing made of copper-nickel alloy is extensively used in making desalination plants for converting sea water into fresh water. 

Trichloroethanol may be used analogously. The 2,2,2-trichloroethyl (Tee) group is best removed by reduction with copper-zinc alloy in DMF at 30 °C (F. Eckstein, nucleic acid synthesis see section 4.1.1. 

TABLE 11.57 Type E Thermocouples Nickel-Chromium Alloy vs. Copper-Nickel Alloy Thermoelectric voltage in millivolts reference junction at 0°C. 

The lead—copper phase diagram (1) is shown in Figure 9. Copper is an alloying element as well as an impurity in lead. The lead—copper system has a eutectic point at 0.06% copper and 326°C. In lead refining, the copper content can thus be reduced to about 0.08% merely by cooling. Further refining requites chemical treatment. The solubiUty of copper in lead decreases to about 0.005% at 0°C. 

Extmded or roUed lead—copper alloys contain a uniform dispersion of copper particles in a lead matrix. Because the soHd solubiUty of copper in lead is very low, copper particles in the matrix remain stable up to near the melting point of lead, maintaining uniform grain size even at elevated temperature. 

Economic Aspects. Lithium metal is available commercially in ingots, special shapes, shot, and dispersions. Ingots are sold in 0.11-, 0.23-, 0.45-, and 0.91-kg sizes. Special shapes include foil, wire, and rod. Lithium is available in hermetically sealed copper cartridges and in sealed copper tubes for use in treating molten copper and copper-base alloys. Shot is sold in 1.19—4.76 mm (16—4 mesh) sizes. Lithium dispersions (30% in mineral oil) of 10—50-p.m particle size are used primarily in organic chemical reactions. Dispersions in other solvents and of other size fractions can be suppHed. 

The electrorefining of many metals can be carried out using molten salt electrolytes, but these processes are usually expensive and have found Httie commercial use in spite of possible technical advantages. The only appHcation on an industrial scale is the electrorefining of aluminum by the three-layer process. The density of the molten salt electrolyte is adjusted so that a pure molten aluminum cathode floats on the electrolyte, which in turn floats on the impure anode consisting of a molten copper—aluminum alloy. The process is used to manufacture high purity aluminum. 

The first reported use of nickel [7440-02-0] Ni, was in a nickel—copper—2inc alloy produced in China in the Middle Ages and perhaps earlier. Alloys of nickel may have been used in prehistoric times. The metal was first isolated for analytical study in the mid-1700s by Axel Cronstedt, who named it nickel, which derives from the German word kupfemickel, or false copper. 

Nickel—Copper. In the soHd state, nickel and copper form a continuous soHd solution. The nickel-rich, nickel—copper alloys are characterized by a good compromise of strength and ductihty and are resistant to corrosion and stress corrosion ia many environments, ia particular water and seawater, nonoxidizing acids, neutral and alkaline salts, and alkaUes. These alloys are weldable and are characterized by elevated and high temperature mechanical properties for certain appHcations. The copper content ia these alloys also easure improved thermal coaductivity for heat exchange. MONEL alloy 400 is a typical nickel-rich, nickel—copper alloy ia which the nickel content is ca 66 wt %. MONEL alloy K-500 is essentially alloy 400 with small additions of aluminum and titanium. Aging of alloy K-500 results in very fine y -precipitates and increased strength (see also Copper alloys). 

ALkylamines are corrosive to copper, copper-containing alloys (brass), aluminum, 2inc, 2inc alloy, and galvani2ed surfaces. Aqueous solutions of aLkylamines slowly etch glass as a consequence of the basic properties of the amines in water. Carbon or stainless steel vessels and piping have been used satisfactorily for handling aLkylamines and, as noted above, some aLkylamines can act as corrosion inhibitors in boiler appHcations. 

Copper. Domestic mine production of copper metal in 1994 was over 1,800,000 t. Whereas U.S. copper production increased in the 1980s and 1990s, world supply declined in 1994. There are eight primary and five secondary smelters, nine electrolytic and six fire refiners, and fifteen solvent extraction—electro winning (SX—EW) plants. Almost 540,000 t/yr of old scrap copper and alloy are recycled in the United States accounting for - 24% of total U.S. consumption (11). New scrap accounted for 825,000 t of contained copper. Almost 80% of the new scrap was consumed by brass mills. The ratio of new-to-old scrap is about 60 40% representing 38% of U.S. supply. 

The New York Commodity Exchange (Comex) prices for cathode copper in January 1993, 1994, and 1994 were 2.218/kg, 1.844/kg, and 3.084/kg, respectively. The primary uses for copper metal and alloy are constmction, 42% electrical/electronic, 24% industrial machinery, 13% transportation equipment, 11% and consumer/general products, 10%. Copper compounds for use in agriculture and industry account for about 1% of total copper consumption. 

Molten tin wets and adheres readily to clean iron, steel, copper, and copper-base alloys, and the coating is bright. It provides protection against oxidation of the coated metal and aids in subsequent fabrication because it is ductile and solderable. Tin coatings can be appHed to most metals by electro deposition (see Electroplating). 

Tin is used in various industrial appHcations as cast and wrought forms obtained by rolling, drawing, extmsion, atomizing, and casting tinplate, ie, low carbon steel sheet or strip roUed to 0.15—0.25 mm thick and thinly coated with pure tin tin coatings and tin alloy coatings appHed to fabricated articles (as opposed to sheet or strip) of steel, cast iron, copper, copper-base alloys, and aluminum tin alloys and tin compounds. 

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