Silver

Silver is a chemical element; it has symbol Ag () and atomic number 47. A soft, whitish-gray, lustrous transition metal, it exhibits the highest electrical conductivity, thermal conductivity, and reflectivity of any metal. Silver is found in the Earth's crust in the pure, free elemental form ("native silver"), as an alloy with gold and other metals, and in minerals such as argentite and chlorargyrite. Most silver is produced as a byproduct of copper, gold, lead, and zinc refining.

Silver has long been valued as a precious metal, commonly sold and marketed beside gold and platinum. Silver metal is used in many bullion coins, sometimes alongside gold: while it is more abundant than gold, it is much less abundant as a native metal. Its purity is typically measured on a per-mille basis; a 94%-pure alloy is described as "0.940 fine". As one of the seven metals of antiquity, silver has had an enduring role in most human cultures. In terms of scarcity, silver is the most abundant of the big three precious metals, platinum, gold, and silver; among these, platinum is the rarest, with around 139 troy ounces of silver mined for every one of platinum.

Other than in currency and as an investment medium (coins and bullion), silver is used in solar panels, water filtration, jewellery, ornaments, high-value tableware and utensils (hence the term "silverware"), in electrical contacts and conductors, in specialised mirrors, window coatings, in catalysis of chemical reactions, as a colorant in stained glass, and in specialised confectionery. Its compounds are used in photographic and X-ray film. Dilute solutions of silver nitrate and other silver compounds are used as disinfectants and microbiocides (oligodynamic effect), added to bandages, wound-dressings, catheters, and other medical instruments.

Characteristics

thumb|left|Silver bullion bar, 1000 ounces

thumb|left|upright|Silver is extremely ductile and, like gold, can be drawn into a wire one atom wide.

Silver is similar in its physical and chemical properties to its two vertical neighbours in group 11 of the periodic table: copper, and gold. Its 47 electrons are arranged in the configuration [Kr]4d¹⁰5s¹, similarly to copper ([Ar]3d¹⁰4s¹) and gold ([Xe]4f¹⁴5d¹⁰6s¹); group 11 is one of the few groups in the d-block which has a completely consistent set of electron configurations. Unlike metals with incomplete d-shells, metallic bonds in silver are lacking a covalent character and are relatively weak. This observation explains the low hardness and high ductility of single crystals of silver.

Silver has a brilliant, white, metallic lustre that can take a high polish, and which is so characteristic that the name of the metal itself has become a colour name. Protected silver has greater optical reflectivity than aluminium at all wavelengths longer than ~450 nm. At wavelengths shorter than 450 nm, silver's reflectivity is inferior to that of aluminium and drops to zero near 310 nm.

Very high electrical and thermal conductivity are common to the elements in group 11, because their single s electron is free and does not interact with the filled d subshell, as such interactions (which occur in the preceding transition metals) lower electron mobility. The thermal conductivity of silver is among the highest of all materials, although the thermal conductivity of carbon (in the diamond allotrope) and superfluid helium-4 are higher. The electrical conductivity of silver is the highest of all metals, greater even than copper. Silver also has the lowest contact resistance of any metal.

Silver readily forms alloys with copper, gold, and zinc. Zinc-silver alloys with low zinc concentration may be considered as face-centred cubic solid solutions of zinc in silver, as the structure of the silver is largely unchanged while the electron concentration rises as more zinc is added. Increasing the electron concentration further leads to body-centred cubic (electron concentration 1.5), complex cubic (1.615), and hexagonal close-packed phases (1.75). this value is very important because of the importance of silver compounds, particularly halides, in gravimetric analysis.

Twenty-eight radioisotopes have been characterised, the most stable being ¹⁰⁵Ag with a half-life of 41.29 days, ¹¹¹Ag with a half-life of 7.45 days, and ¹¹²Ag with a half-life of 3.13 hours. Silver has numerous nuclear isomers, the most stable being ^108mAg (t_1/2 = 418 years), ^110mAg (t_1/2 = 249.79 days) and ^106mAg (t_1/2 = 8.28 days). All of the remaining radioactive isotopes have half-lives of less than an hour, and the majority of these have half-lives of less than three minutes.

Isotopes of silver range in atomic mass from 92.950 Da (⁹³Ag) to 129.950 Da (¹³⁰Ag); the primary decay mode before the most abundant stable isotope, ¹⁰⁷Ag, is electron capture and the primary mode after is beta decay. The primary decay products before ¹⁰⁷Ag are palladium (element 46) isotopes, and the primary products after are cadmium (element 48) isotopes. ¹⁰⁷Pd–¹⁰⁷Ag correlations observed in bodies that have clearly been melted since the accretion of the Solar System must reflect the presence of unstable nuclides in the early Solar System.

Chemistry

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|+ Oxidation states and molecular geometries of silver Unlike copper, for which the larger hydration energy of Cu²⁺ as compared to Cu⁺ is the reason why the former is the more stable in aqueous solution and solids despite lacking the stable filled d-subshell of the latter, with silver this effect is swamped by its larger second ionisation energy. Hence, Ag⁺ is the stable species in aqueous solution and solids, with Ag²⁺ being much less stable as it oxidises water. Due to its full d-subshell, silver in its main +1 oxidation state exhibits relatively few properties of the transition metals proper from groups 4 to 10, forming rather unstable organometallic compounds, forming linear complexes showing very low coordination numbers like 2, and forming an amphoteric oxide as well as Zintl phases like the post-transition metals. Unlike the preceding transition metals, the +1 oxidation state of silver is stable even in the absence of π-acceptor ligands.

The three main forms of deterioration in historical silver artifacts are tarnishing, formation of silver chloride due to long-term immersion in salt water, as well as reaction with nitrate ions or oxygen. Fresh silver chloride is pale yellow, becoming purplish on exposure to light; it projects slightly from the surface of the artifact or coin. The precipitation of copper in ancient silver can be used to date artifacts, as copper is nearly always a constituent of silver alloys.

Silver metal is attacked by strong oxidant such as potassium permanganate () and potassium dichromate (), and in the presence of potassium bromide (). These compounds are used in photography to bleach silver images, converting them to silver bromide that can either be fixed with thiosulfate or redeveloped to intensify the original image. Silver forms cyanide complexes (silver cyanide) that are soluble in water in the presence of an excess of cyanide ions. Silver cyanide solutions are used in electroplating of silver.

The common oxidation states of silver are (in order of commonness): +1 (the most stable state; for example, silver nitrate, AgNO₃); +2 (highly oxidising; for example, silver(II) fluoride, AgF₂); and even very rarely +3 (extreme oxidising; for example, potassium tetrafluoroargentate(III), KAgF₄). The +3 state requires very strong oxidising agents to attain, such as fluorine or peroxodisulfate, and some silver(III) compounds react with atmospheric moisture and attack glass. Indeed, silver(III) fluoride is usually obtained by reacting silver or silver monofluoride with the strongest known oxidising agent, krypton difluoride.

Compounds

Oxides and chalcogenides

thumb|right|Silver(I) sulfide

Silver and gold have rather low chemical affinities for oxygen, lower than copper, and it is therefore expected that silver oxides are thermally quite unstable. Soluble silver(I) salts precipitate dark-brown silver(I) oxide, Ag₂O, upon the addition of alkali. (The hydroxide AgOH exists only in solution; otherwise it spontaneously decomposes to the oxide.) Silver(I) oxide is very easily reduced to metallic silver, and decomposes to silver and oxygen above 160 °C. This and other silver(I) compounds may be oxidised by the strong oxidising agent peroxodisulfate to black AgO, a mixed silver(I,III) oxide of formula Ag^IAg^IIIO₂. Some other mixed oxides with silver in non-integral oxidation states, namely Ag₂O₃ and Ag₃O₄, are also known, as is Ag₃O which behaves as a metallic conductor.

In stark contrast to this, all four silver(I) halides are known. The fluoride, chloride, and bromide have the sodium chloride structure, but the iodide has three known stable forms at different temperatures; that at room temperature is the cubic zinc blende structure. They can all be obtained by the direct reaction of their respective elements.

:X⁻ + hν → X + e⁻ (excitation of the halide ion, which gives up its extra electron into the conduction band)

:Ag⁺ + e⁻ → Ag (liberation of a silver ion, which gains an electron to become a silver atom)

The process is not reversible because the silver atom liberated is typically found at a crystal defect or an impurity site, so that the electron's energy is lowered enough that it is "trapped". It is often used for gravimetric analysis, exploiting the insolubility of the heavier silver halides which it is a common precursor to.

Yellow silver carbonate, Ag₂CO₃ can be easily prepared by reacting aqueous solutions of sodium carbonate with a deficiency of silver nitrate. Its principal use is for the production of silver powder for use in microelectronics. It is reduced with formaldehyde, producing silver free of alkali metals:

:Ag₂CO₃ + CH₂O → 2 Ag + 2 CO₂ + H₂

Silver carbonate is also used as a reagent in organic synthesis such as the Koenigs–Knorr reaction. In the Fétizon oxidation, silver carbonate on celite acts as an oxidising agent to form lactones from diols. It is also employed to convert alkyl bromides into alcohols. and silver acetylide, Ag₂C₂, formed when silver reacts with acetylene gas in ammonia solution.

By far the most important oxidation state for silver in complexes is +1. The Ag⁺ cation is diamagnetic, like its homologues Cu⁺ and Au⁺, as all three have closed-shell electron configurations with no unpaired electrons: its complexes are colourless provided the ligands are not too easily polarised such as I⁻. Ag⁺ forms salts with most anions, but it is reluctant to coordinate to oxygen and thus most of these salts are insoluble in water: the exceptions are the nitrate, perchlorate, and fluoride. The tetracoordinate tetrahedral aqueous ion [Ag(H₂O)₄]⁺ is known, but the characteristic geometry for the Ag⁺ cation is 2-coordinate linear. For example, silver chloride dissolves readily in excess aqueous ammonia to form [Ag(NH₃)₂]⁺; silver salts are dissolved in photography due to the formation of the thiosulfate complex [Ag(S₂O₃)₂]³⁻; and cyanide extraction for silver (and gold) works by the formation of the complex [Ag(CN)₂]⁻. Silver cyanide forms the linear polymer {Ag–C≡N→Ag–C≡N→}; silver thiocyanate has a similar structure, but forms a zigzag instead because of the sp³-hybridized sulfur atom. Chelating ligands are unable to form linear complexes and thus silver(I) complexes with them tend to form polymers; a few exceptions exist, such as the near-tetrahedral diphosphine and diarsine complexes [Ag(L–L)₂]⁺.

Organometallic

Under standard conditions, silver does not form simple carbonyls, due to the weakness of the Ag–C bond. A few are known at very low temperatures around 6–15 K, such as the green, planar paramagnetic Ag(CO)₃, which dimerises at 25–30 K, probably by forming Ag–Ag bonds. Additionally, the silver carbonyl [Ag(CO)][B(OTeF₅)₄] is known. Polymeric AgLX complexes with alkenes and alkynes are known, but their bonds are thermodynamically weaker than even those of the platinum complexes (though they are formed more readily than those of the analogous gold complexes): they are also quite unsymmetrical, showing the weak π bonding in group 11. Ag–C σ bonds may also be formed by silver(I), like copper(I) and gold(I), but the simple alkyls and aryls of silver(I) are even less stable than those of copper(I) (which tend to explode under ambient conditions). For example, poor thermal stability is reflected in the relative decomposition temperatures of AgMe (−50 °C) and CuMe (−15 °C) as well as those of PhAg (74 °C) and PhCu (100 °C).

The C–Ag bond is stabilised by perfluoroalkyl ligands, for example in AgCF(CF₃)₂. Alkenylsilver compounds are also more stable than their alkylsilver counterparts. Silver-NHC complexes are easily prepared, and are commonly used to prepare other NHC complexes by displacing labile ligands. For example, the reaction of the bis(NHC)silver(I) complex with bis(acetonitrile)palladium dichloride or chlorido(dimethyl sulfide)gold(I):

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Intermetallic

thumb|upright=1.14|right|Different colors of silver–copper–gold alloys

Silver forms alloys with most other elements on the periodic table. The elements from groups 1–3, except for hydrogen, lithium, and beryllium, are very miscible with silver in the condensed phase and form intermetallic compounds; those from groups 4–9 are only poorly miscible; the elements in groups 10–14 (except boron and carbon) have very complex Ag–M phase diagrams and form the most commercially important alloys; and the remaining elements on the periodic table have no consistency in their Ag–M phase diagrams. By far the most important such alloys are those with copper: most silver used for coinage and jewellery is in reality a silver–copper alloy, and the eutectic mixture is used in vacuum brazing. The two metals are completely miscible as liquids but not as solids; their importance in industry comes from the fact that their properties tend to be suitable over a wide range of variation in silver and copper concentration, although most useful alloys tend to be richer in silver than the eutectic mixture (71.9% silver and 28.1% copper by weight, and 60.1% silver and 28.1% copper by atom).

Most other binary alloys are of little use: for example, silver–gold alloys are too soft and silver–cadmium alloys too toxic. Ternary alloys have much greater importance: dental amalgams are usually silver–tin–mercury alloys, silver–copper–gold alloys are very important in jewellery (usually on the gold-rich side) and have a vast range of hardnesses and colours, silver–copper–zinc alloys are useful as low-melting brazing alloys, and silver–cadmium–indium (involving three adjacent elements on the periodic table) is useful in nuclear reactors because of its high thermal neutron capture cross-section, good conduction of heat, mechanical stability, and resistance to corrosion in hot water. the three metals of group 11, copper, silver, and gold, occur in the elemental form in nature and were probably used as the first primitive forms of money as opposed to simple bartering. Unlike copper, silver did not lead to the growth of metallurgy, on account of its low structural strength; it was more often used ornamentally or as money. Since silver is more reactive than gold, supplies of native silver were much more limited than those of gold. the Egyptians are thought to have separated gold from silver by heating the metals with salt, and then reducing the silver chloride produced to the metal. these techniques did not spread widely until later,

when it spread throughout the region and beyond. The stability of the Roman currency relied to a high degree on the supply of silver bullion, mostly from Spain, which Roman miners produced on a scale unparalleled before the discovery of the New World. Reaching a peak production of 200 tonnes per year, an estimated silver stock of 10,000 tonnes circulated in the Roman economy in the middle of the second century AD, five to ten times larger than the combined amount of silver available to medieval Europe and the Abbasid Caliphate around AD 800. The Romans also recorded the extraction of silver in central and northern Europe in the same time period. This production came to a nearly complete halt with the fall of the Roman Empire, not to resume until the time of Charlemagne: by then, tens of thousands of tonnes of silver had already been extracted.

Central Europe became the centre of silver production during the Middle Ages, as the Mediterranean deposits exploited by the ancient civilisations had been exhausted. Silver mines were opened in Bohemia, Saxony, Alsace, the Lahn region, Siegerland, Silesia, Hungary, Norway, Steiermark, Schwaz, and the southern Black Forest. Most of these ores were quite rich in silver and could simply be separated by hand from the remaining rock and then smelted; some deposits of native silver were also encountered. Many of these mines were soon exhausted, but a few of them remained active until the Industrial Revolution, before which the world production of silver was around a meagre 50 tonnes per year.

With the discovery of America and the plundering of silver by the Spanish conquistadors, Central and South America became the dominant producers of silver until around the beginning of the 18th century, particularly Peru, Bolivia, Chile, and Argentina: Much of this silver ended up in the hands of the Chinese. A Portuguese merchant in 1621 noted that silver "wanders throughout all the world... before flocking to China, where it remains as if at its natural centre". Still, much of it went to Spain, allowing Spanish rulers to pursue military and political ambitions in both Europe and the Americas. "New World mines", concluded several historians, "supported the Spanish empire."

In the 19th century, primary production of silver moved to North America, particularly Canada, Mexico, and Nevada in the United States: some secondary production from lead and zinc ores also took place in Europe, and deposits in Siberia and the Russian Far East as well as in Australia were mined. Ovid's Metamorphoses contains another retelling of the story, containing an illustration of silver's metaphorical use of signifying the second-best in a series, better than bronze but worse than gold:

In folklore, silver was commonly thought to have mystic powers: for example, a bullet cast from silver is often supposed in such folklore the only weapon that is effective against a werewolf, witch, or other monsters. From this the idiom of a silver bullet developed into figuratively referring to any simple solution with very high effectiveness or almost miraculous results, as in the widely discussed software engineering paper "No Silver Bullet". Other powers attributed to silver include detection of poison and facilitation of passage into the mythical realm of fairies. Ethically, silver also symbolizes greed and degradation of consciousness; this is the negative aspect, the perverting of its value.

Occurrence and production

thumb|World production of silver

The abundance of silver in the Earth's crust is 0.08 parts per million, almost exactly the same as that of mercury. It mostly occurs in sulfide ores, especially acanthite and argentite, Ag₂S. Argentite deposits sometimes also contain native silver when they occur in reducing environments, and when in contact with salt water they are converted to chlorargyrite (including horn silver), AgCl, which is prevalent in Chile and New South Wales. Most other silver minerals are silver pnictides or chalcogenides; they are generally lustrous semiconductors. Most true silver deposits, as opposed to argentiferous deposits of other metals, came from Tertiary vulcanism.

The principal sources of silver are the ores of copper, copper-nickel, lead, and lead-zinc obtained from Peru, Bolivia, Mexico, China, Australia, Chile, Poland and Serbia. Top near-term mine development projects through 2015 are Pascua Lama (Chile), Navidad (Argentina), Jaunicipio (Mexico), Malku Khota (Bolivia), and Hackett River (Canada).

Silver is usually found in nature combined with other metals, or in minerals that contain silver compounds, generally in the form of sulfides such as galena (lead sulfide) or cerussite (lead carbonate). So the primary production of silver requires the smelting and then cupellation of argentiferous lead ores, a historically important process. Lead melts at 327 °C, lead oxide at 888 °C and silver melts at 960 °C. To separate the silver, the alloy is melted again at the high temperature of 960 °C to 1000 °C in an oxidising environment. The lead oxidises to lead monoxide, then known as litharge, which captures the oxygen from the other metals present. The liquid lead oxide is removed or absorbed by capillary action into the hearth linings.

: (s) + 2(s) + (g) → 2(absorbed) + Ag(l)

Today, silver metal is primarily produced instead as a secondary byproduct of electrolytic refining of copper, lead, and zinc, and by application of the Parkes process on lead bullion from ore that also contains silver.

In marine environments

Silver concentration is low in seawater (pmol/L). Levels vary by depth and between water bodies. Dissolved silver concentrations range from 0.3 pmol/L in coastal surface waters to 22.8 pmol/L in pelagic deep waters. Analysing the presence and dynamics of silver in marine environments is difficult due to these particularly low concentrations and complex interactions in the environment. Although a rare trace metal, concentrations are greatly impacted by fluvial, aeolian, atmospheric, and upwelling inputs, as well as anthropogenic inputs via discharge, waste disposal, and emissions from industrial companies. Other internal processes such as decomposition of organic matter may be a source of dissolved silver in deeper waters, which feeds into some surface waters through upwelling and vertical mixing. Silver is taken up by plankton in the photic zone, remobilized with depth, and enriched in deep waters. Silver is transported from the Atlantic to the other oceanic water masses.

There is not an extensive amount of data focused on how marine life is affected by silver despite the likely deleterious effects it could have on organisms through bioaccumulation, association with particulate matters, and sorption.

In one study, the presence of excess ionic silver and silver nanoparticles caused bioaccumulation effects on zebrafish organs and altered the chemical pathways within their gills. In addition, very early experimental studies demonstrated how the toxic effects of silver fluctuate with salinity and other parameters, as well as between life stages and different species such as finfish, molluscs, and crustaceans. Another study found raised concentrations of silver in the muscles and liver of dolphins and whales, indicating pollution of this metal within recent decades. Silver is not an easy metal for an organism to eliminate and elevated concentrations can cause death.

Monetary use

thumb|An [[American Silver Eagle bullion coin, minted from .999 fine silver]]

The earliest known coins were minted in the kingdom of Lydia in Asia Minor around 600 BC. The coins of Lydia were made of electrum, which is a naturally occurring alloy of gold and silver, that was available within the territory of Lydia. the Roman denarius, the Islamic dirham, the karshapana from ancient India and rupee from the time of the Mughal Empire (grouped with copper and gold coins to create a trimetallic standard), and the Spanish dollar.

The ratio between the amount of silver used for coinage and that used for other purposes has fluctuated greatly over time; for example, in wartime, more silver tends to have been used for coinage to finance the war.

Today, silver bullion has the ISO 4217 currency code XAG, one of only four precious metals to have one (the others being platinum, palladium, and gold). Silver coins are produced from cast rods or ingots, rolled to the correct thickness, heat-treated, and then used to cut blanks from. These blanks are then milled and minted in a coining press; modern coining presses can produce 8,000 silver coins per hour. This price is determined by several major international banks and is used by London bullion market members for trading that day. Prices are most commonly shown as the United States dollar (USD), the Pound sterling (GBP), and the Euro (EUR).

Applications

Jewellery and silverware

thumb|[[Repoussé and chasing|Embossed silver sarcophagus of Saint Stanislaus in the Wawel Cathedral was created in main centres of the 17th century European silversmithery – Augsburg and Gdańsk in fact, most silverware is only silver-plated rather than made out of pure silver; the silver is normally put in place by electroplating. Silver-plated glass (as opposed to metal) is used for mirrors, vacuum flasks, and Christmas tree decorations. The silver ion is bioactive and in sufficient concentration readily kills bacteria in vitro. Silver ions interfere with enzymes in the bacteria that transport nutrients, form structures, and synthesise cell walls; these ions also bond with the bacteria's genetic material. Silver and silver nanoparticles are used as an antimicrobial in a variety of industrial, healthcare, and domestic application: for example, infusing clothing with nanosilver particles thus allows them to stay odourless for longer. Silver diammine fluoride, the fluoride salt of a coordination complex with the formula [Ag(NH₃)₂]F, is a topical medicament (drug) used to treat and prevent dental caries (cavities) and relieve dentinal hypersensitivity.

Electronics

Silver is very important in electronics for conductors and electrodes on account of its high electrical conductivity even when tarnished. Bulk silver and silver foils were used to make vacuum tubes, and continue to be used today in the manufacture of semiconductor devices, circuits, and their components. For example, silver is used in high quality connectors for RF, VHF, and higher frequencies, particularly in tuned circuits such as cavity filters where conductors cannot be scaled by more than 6%. Printed circuits and RFID antennas are made with silver paints, Powdered silver and its alloys are used in paste preparations for conductor layers and electrodes, ceramic capacitors, and other ceramic components.

Brazing alloys

Silver-containing brazing alloys are used for brazing metallic materials, mostly cobalt, nickel, and copper-based alloys, tool steels, and precious metals. The basic components are silver and copper, with other elements selected according to the specific application desired: examples include zinc, tin, cadmium, palladium, manganese, and phosphorus. Silver provides increased workability and corrosion resistance during usage.

Chemical equipment

Silver is useful in the manufacture of chemical equipment on account of its low chemical reactivity, high thermal conductivity, and being easily workable. Silver crucibles (alloyed with 0.15% nickel to avoid recrystallisation of the metal at red heat) are used for carrying out alkaline fusion. Copper and silver are also used when doing chemistry with fluorine. Equipment made to work at high temperatures is often silver-plated. Silver and its alloys with gold are used as wire or ring seals for oxygen compressors and vacuum equipment.

Catalysis

Silver metal is a good catalyst for oxidation reactions; in fact it is somewhat too good for most purposes, as finely divided silver tends to result in complete oxidation of organic substances to carbon dioxide and water, and hence coarser-grained silver tends to be used instead. For instance, 15% silver supported on α-Al₂O₃ or silicates is a catalyst for the oxidation of ethylene to ethylene oxide at 230–270 °C. Dehydrogenation of methanol to formaldehyde is conducted at 600–720 °C over silver gauze or crystals as the catalyst, as is dehydrogenation of isopropanol to acetone. In the gas phase, glycol yields glyoxal and ethanol yields acetaldehyde, while organic amines are dehydrated to nitriles.

The market for silver nitrate and silver halides for photography has rapidly declined with the rise of digital cameras. From the peak global demand for photographic silver in 1999 (267,000,000 troy ounces or 8,304.6 tonnes) the market contracted almost 70% by 2013.

Nanoparticles

Nanosilver particles, between 10 and 100 nanometres in size, are used in many applications. They are used in conductive inks for printed electronics, and have a much lower melting point than larger silver particles of micrometre size. They are also used medicinally in antibacterials and antifungals in much the same way as larger silver particles.

Miscellanea

thumb|A tray of [[South Asian sweets, with some pieces covered with shiny silver vark]]

Pure silver metal is used as a food colouring. It has the E174 designation and is approved in the European Union. Traditional Indian and Pakistani dishes sometimes include decorative silver foil known as vark, and in various other cultures, silver dragée are used to decorate cakes, cookies, and other dessert items.

Photochromic lenses include silver halides, so that ultraviolet light in natural daylight liberates metallic silver, darkening the lenses. The silver halides are reformed in lower light intensities. Colourless silver chloride films are used in radiation detectors. Zeolite sieves incorporating Ag⁺ ions are used to desalinate seawater during rescues, using silver ions to precipitate chloride as silver chloride. Silver is also used for its antibacterial properties for water sanitisation, but the application of this is limited by limits on silver consumption. Colloidal silver is similarly used to disinfect closed swimming pools; while it has the advantage of not giving off a smell like hypochlorite treatments do, colloidal silver is not effective enough for more contaminated open swimming pools. Small silver iodide crystals are used in cloud seeding to cause rain.

The Texas Legislature designated silver the official precious metal of Texas in 2007.

Precautions

Silver compounds have low toxicity compared to those of most other heavy metals, as they are poorly absorbed by the human body when ingested, and that which does get absorbed is rapidly converted to insoluble silver compounds or complexed by metallothionein. Silver fluoride and silver nitrate are caustic and can cause tissue damage, resulting in gastroenteritis, diarrhoea, falling blood pressure, cramps, paralysis, or respiratory arrest. Animals repeatedly dosed with silver salts have been observed to experience anaemia, slowed growth, necrosis of the liver, and fatty degeneration of the liver and kidneys; rats implanted with silver foil or injected with colloidal silver have been observed to develop localised tumours. Parenterally administered colloidal silver causes acute silver poisoning. Some waterborne species are particularly sensitive to silver salts and those of the other precious metals; in most situations, silver is not a serious environmental hazard.

Bibliography

External links

• Silver at The Periodic Table of Videos (University of Nottingham)
• The Silver Institute, industry association website
• Collection of silver items and samples from Theodore Gray
• Silver entry in the NIOSH Pocket Guide to Chemical Hazards published by the U.S. Centers for Disease Control and Prevention's National Institute for Occupational Safety and Health
• Silver prices – current spot prices on the global commodities markets, from Bloomberg L.P.