Alloys precious metal

Aluminum and aluminum alloys Copper and copper alloys Rare-earth and rare-earth-like metals and alloys Low-melting metals and alloys Miscellaneous nonferrous metals and alloys Nickel and nickel alloys Precious metals and alloys Reactive and refractory metals and alloys... 

Water Atomization -100 Standard deviation 1.7-2.4 Fe, Cu, Cu alloys, Stainless steels. Tool steels, Ni alloys, Precious metals 104-106 400 15-60 Steel iron 0.5-5 Stainless steel Cu alloys High volume, Low cost Powder purity shapeXow EE... 

Source American Society for Testing and Materials, 1976 Annual Book of ASTMStandards part 8, Nonferrous Metals-Nickel, Lead and Tin Alloys, Precious Metals, Primary Metals Reactive Metals, ASTM, Philadelphia, 1976. 

Melting, Smelting, and Casting of Metals. Molded graphite has numerous e iplications in the processing of ferrous and non-ferrous metals and alloys such as copper, copper-nickel, brass, bronze, zinc, aluminum alloys, nickel and its alloys, precious metals, and grey and ductile irons.l°ll °l The wide variety of these applications is shown in the following partial list ... 

Skiving is a variant in which the base metal surface oxides are mechanically removed foUowed immediately by pressure rolling of a precious metal or alloy strip. This is commonly used for inlays for electrical contacts and for jewelry fabrication. The common inlay materials include gold, silver, copper, brass, and solder. No heat is needed, and the coating is appHed only to designated areas so there is Htde waste (3,50). 

GoldJilloys, Wrought Type. Two types of wrought gold alloys were formerly recognized by the ADA specification no. 7 for the fabrication of orthodontic and prosthetic dental appHances, ie, type I, high-precious-metal alloys, and type II, low-precious-metal alloys (gold color). Alloys of this type are seldom used in the United States they have been replaced by stainless steels and nickel—titanium alloys. 

JS/oble Metals. Noble or precious metals, ie, Pt, Pd, Ag, and Au, are ftequendy alloyed with the closely related metals, Ru, Rh, Os, and Ir (see Platinum-GROUP metals). These are usually supported on a metal oxide such as a-alumina, a-Al202, or siUca, Si02. The most frequently used precious metal components are platinum [7440-06-4J, Pt, palladium [7440-05-3] Pd, and rhodium [7440-16-6] Rh. The precious metals are more commonly used because of the abiUty to operate at lower temperatures. As a general rule, platinum is more active for the oxidation of paraffinic hydrocarbons palladium is more active for the oxidation of unsaturated hydrocarbons and CO (19). 

Toxic heavy metals and ions, eg, Pb, Hg, Bi, Sn, Zn, Cd, Cu, and Fe, may form alloys with catalytic metals (24). Materials such as metallic lead, ziac, and arsenic react irreversibly with precious metals and make the surface unavailable for catalytic reactions. Poisoning by heavy metals ordinarily destroys the activity of a precious-metal catalyst (8). 

The precious metals are many times the cost of the base metals and, therefore, are limited to specialized applications or to those in which process conditions are highly demanding (e.g., where conditions are too corrosive for base metals and temperatures too high for plastics where base metal contamination must be avoided, as in the food and pharmaceutical industries or where plastics cannot be used because of heat transfer requirements and for special applications such as bursting discs in pressure vessels). The physical and mechanical properties of precious metals and their alloys used in process plants are given in Table 3.38. 

The copper-bearing aluminium alloys are more noble than most other aluminium alloys and can accelerate attack on these, notably in sea-water. Mercury and all the precious metals are harmful to aluminium. 

There are obviously situations which demand considerable over-design of a cathodic protection system, in particular where regular and efficient maintenance of anodes is not practical, or where temporary failure of the system could cause costly damage to plant or product. Furthermore, contamination of potable waters by chromium-containing or lead-based alloy anodes must lead to the choice of the more expensive, but more inert, precious metal-coated anodes. The choice of material is then not unusual in being one of economics coupled with practicability. 

Laister and Benham have shown that under more arduous conditions (immersion for 6 months in sea-water) a minimum thickness of 0-025 mm of silver is required to protect steel, even when the silver is itself further protected by a thin rhodium coating. In similar circumstances brass was completely protected by 0 012 5 mm of silver. The use of an undercoating deposit of intermediate electrode potential is generally desirable when precious metal coatings are applied to more reactive base metals, e.g. steel, zinc alloys and aluminium, since otherwise corrosion at discontinuities in the coating will be accelerated by the high e.m.f. of the couple formed between the coating and the basis metal. The thickness of undercoat may have to be increased substantially above the values indicated if the basis metal is affected by special defects such as porosity. 

In view of the high cost, when tarnish resistance of the surface is the only requirement it is customary to use the thinnest possible coatings of rhodium (0-000 25-0-000 5 mm). Since rhodium deposits in this thickness range, like thin electrodeposits of other metals, show significant porosity, readily corrodible metals, e.g. steel, zinc-base alloys, etc. must be provided with an undercoating deposit, usually of silver or nickel, which is sufficiently thick to provide a fairly high level of protection to the basis metal even before the final precious metal deposit is applied, and, in this way, to prevent accelerated electrochemical corrosion at pores in the rhodium deposit. 

Chemical reduction of metal salts in solution is the most widely used method of preparation of metal nanoparticles, especially in laboratories. In general, the reducing reagents are added into the solution of the precursor ions, but in some cases, a solvent works as a reductant. Various reducing reagents have been proposed to prepare metal nanoparticles. Ethanol or small alcohols can reduce precious metal ions such as Au, Pt", Pd, Ag, and so on [3j. Polymer-stabilized precious metal nanoparticles and their alloy particles can be used as good catalysts for various reactions. Polyols, such as ethylene glycol, were... 

Moving on from preparation of homogenous Pt alloy particles to tailoring of core-and-sheU alloy particles, targeting (i) further lowering of the mass of precious metal per unit power output and (ii) further boost of catalytic activity per square centimeter of catalyst area [Zhang et al., 2004]. 

Ancient artisans were able to confer special colourings to their artefacts by applying particular techniques and treatments, which were lost in later centuries. They were also able to give copper based alloys the appearance of precious metals. Some of these special methods have been discovered and identified on ancient objects. The most famous of these alloys in Roman times was certainly Corinthian bronze, a copper alloy containing small amounts of precious metals, which acquired a purple-black or blue-black patination... 

Precious metal. This means gold, silver, or platinum group metals, and the principal alloys of those metals. 

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