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CHEMISTRY : Metal Cation Identification


Information on SILVER




  1. General Information

  2. Occurence Uses and Properties

  3. History of the Metal

  4. Compounds
  5. Back to Main Metal List




General Information


Silver (Ag), chemical element, a white, lustrous metal valued for its decorative beauty and electrical conductivity. Silver is loCATed in Group Ib Period 5 of the periodic table, between copper (Period 4) and gold (Period 6), and its physical and chemical properties are intermediate between those two metals.

Silver and gold are two of the noblest--that is, least chemically reactive--of the transition elements, and both are found in nature in the free state. For silver the more important deposits commercially are such compounds as the mineral argentite (silver sulfide, Ag2S), which is usually associated with other sulfides such as those of lead and copper, as well as several other sulfides, some of which contain antimony as well. Silver is found generally in lead ores, copper ores, and cobalt arsenide ores and is also frequently associated with gold in nature. Most silver is derived as a by-product from ores that are mined and processed to obtain these other metals. Gold is most commonly found free, the only compounds of gold in nature being various tellurides.

Silver is a white, lustrous metal and is among the most ductile and malleable ones known. Pure silver has the highest electrical and thermal conductivities of all metals. Gold is a soft, yellow metal that has the highest ductility and malleability of any element.

Silver is less reactive chemically than copper except toward sulfur and hydrogen sulfide, which rapidly blacken silver surfaces. The metal will dissolve in oxidizing acids and in solutions containing cyanide ions in the presence of oxygen or peroxides. Gold is much less reactive and is not attacked by oxygen or sulfur, although it will react readily with halogens or with solutions containing or generating chlorine, such as aqua regia. It also will dissolve in cyanide solutions in presence of air or hydrogen peroxide. Dissolution in cyanide solutions is attributable to the formation of the very stable dicyanoargentate(I), Ag(CN)2-, and dicyanoaurate(I), Au(CN)2-, ions.

As does copper, the elements silver and gold have a single s electron outside a completed d shell, but in spite of the similarity in electronic structures and ionization potentials there are few close resemblances between silver and gold on the one hand and copper on the other.

Both silver and gold find their chief appliCATions in the form of the metals themselves, but silver is also of unique utility as silver chloride in photographic emulsions. Despite the relatively high cost of the material no satisfactory substitute has ever been found.

For silver the pre-eminently important oxidation state in all of its ordinary chemistry is the state +1, although the states +2 and +3 are known. With gold, on the other hand, the state +1 is generally quite unstable, and most of the chemistry of gold involves the state +3.



Occurrence, uses, and properties.


Together with gold, and the platinum-group metals, silver is one of the so-called precious metals. Because of its comparative scarcity, brilliant white colour, malleability, and resistance to atmospheric oxidation, silver has long been used in the manufacture of coins, ornaments, and jewelry. Silver has the highest known electrical and thermal conductivity of all metals and is used in fabriCATing printed electrical circuits and as a vapour-deposited coating for electronic conductors; it is also alloyed with such elements as nickel or palladium for use in electrical contacts. Silver also finds use as a CATalyst for its unique ability to convert ethylene to ethylene oxide, which is a precursor of many organic compounds.

Silver ornaments and decorations have been found in royal tombs dating back as far as 4000 BC. It is probable that both gold and silver were used as money by 800 BC in all countries between the Indus and the Nile.

Silver is widely distributed in nature, but the total amount is quite small when compared with other metals; the metal constitutes 0.05 parts per million of the Earth's crust. Practically all sulfides of lead, copper, and zinc contain some silver. Silver-bearing ores may contain amounts of silver from a trace to several thousand troy ounces per avoirdupois ton, or about 10 percent.

Unlike gold, silver is present in many naturally occurring minerals. The most abundant include argentite (Ag2S) and tetrahedrite. Deposits of native (chemically free, or uncombined) silver are also commercially important.

Because the majority of the ores that contain silver also contain the important metals lead, copper, or zinc or a combination of the three, the silver-bearing fraction of these ores is frequently recovered as a by-product of copper and lead production. Pure silver is then recovered from the crude fraction by a combination of smelting and fire- or electrorefining.

Historically, a major use of silver has been monetary, in the form of reserves of silver bullion and in coins. By the 1960s, however, the demand for silver for industrial purposes, in particular the photographic industry, exceeded the total annual world production.

Use of the metal for sterling and plated silverware, ornaments, jewelry, and similar products has continued to be important. Alloys of silver with copper are harder, tougher, and more fusible than pure silver and are used for jewelry and coinage. The proportion of silver in these alloys is stated in terms of fineness, which means parts of silver per thousand of the alloy. Sterling silver contains 92.5 percent of silver and 7.5 percent of another metal, usually copper; i.e., it has a fineness of 925. Jewelry silver is an alloy containing 80 percent silver and 20 percent copper (800 fine). Gold dental alloys contain about 75 percent gold and 10 percent silver. The yellow gold that is used in jewelry is composed of 53 percent gold, 25 percent silver, and 22 percent copper.

Natural silver consists of a mixture of two stable isotopes: silver-107 and silver-109. The metal does not react with moist air or dry oxygen but is oxidized superficially by moist ozone. It is quickly tarnished at room temperature by sulfur or hydrogen sulfide. In the molten state, silver can dissolve up to 22 times its volume of oxygen; on solidifiCATion, most of the oxygen is expelled, a phenomenon known as the spitting of silver. This can be controlled by the addition of a deoxidant such as charcoal to the molten silver. Silver dissolves readily in nitric acid and in hot concentrated sulfuric acid.



History


Silver was discovered after gold and copper about 4000 BC, when it was used in jewelry and as a medium of exchange. The earliest known workings of significant size were those of the pre-Hittites of Cappadocia in eastern Anatolia. Silver is generally found in the combined state in nature, usually in copper or lead mineralization, and by 2000 BC mining and smelting of silver-bearing lead ores was under way. Lead ores were smelted to obtain an impure lead-silver alloy, which was then fire refined by cupellation. The best-known of the ancient mines were loCATed at the Laurium silver-lead deposit in Greece; this was actively mined from 500 BC to AD 100. Spanish mines were also a major source.

By the 16th century, Spanish conquistadores had discovered and developed silver mines in Mexico, Bolivia, and Peru. These New World mines, much richer in silver, resulted in the rise of South and Central America as the largest silver-producing areas in the world. For the recovery of New World silver, the Patio process was employed. Silver-bearing ore was ground and then mixed with salt, roasted copper ore, and mercury. The mixing was accomplished by tethering mules to a central post on a paved patio (hence the name of the process) and compelling them to walk in a circle through the mixture. The silver was gradually converted to the elemental state in a very finely divided form, from which it was dissolved by the mercury. Periodically, the mercury was collected and distilled to recover the silver, and this was subsequently refined by cupellation. Cyanidation processes supplanted the Patio process in the late 19th century; by that time, the Moebius and Thum Balbach electrorefining processes had been introduced.

In the mid-19th century a large silver deposit was discovered in Nevada. This resulted in the United States becoming the world's largest silver producer until the 20th century, when it was surpassed by Mexico and South America (particularly Peru).



Chemical compounds


In the majority of silver compounds the element has a valence of one. These compounds include such familiar substances as silver chloride (AgCl), silver bromide (AgBr), and silver iodide (AgI). Each of these salts is used extensively in photography. Silver chloride serves as the light-sensitive material in photographic printing papers and, together with silver bromide, in certain films and plates. The iodide is also used in the manufacture of photographic papers and films, as well as in cloud seeding for artificial rainmaking and in some antiseptics. All three halides are derived from silver nitrate (AgNO3), which is the most important of the inorganic silver salts. Besides these other salts, silver nitrate is also the starting material for the production of the silver cyanide used in silver plating.

atomic number 47 atomic weight 107.868 melting point 960.8 C (1,861.4 F) boiling point 2,212 C (4,014 F) specific gravity 10.5 (20 C) valence 1,2 electronic config. 2-8-18-18-1 or (Kr)4d105s1

    Reference: Encyclopędia Britannica, Inc. 1994-2000 ©


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