Monday, December 30, 2013

Thallium (81)


Enjoy these while you can...shipping out next week!

When freshly exposed to air, thallium exhibits a metallic luster, but soon develops a bluish-grey tinge, resembling lead in appearance. A heavy oxide builds up on thallium if left in air, and in the presence of water the hydroxide is formed. The metal is very soft and malleable. It can be cut with a knife.

The element and its compounds are toxic and should be handled carefully. Thallium may cause cancer (though really...what can't in certain amounts???).

•Name: Thallium
•Symbol: Tl
•Atomic number: 81
•Atomic weight: 204.3833 (2) 
•Standard state: solid at 298 K
•CAS Registry ID: 7440-28-0
•Group in periodic table: 13
•Group name: (none)
•Period in periodic table: 6 
•Block in periodic table: p-block
•Color: silvery white
•Classification: Metallic

Historical information
Thallium was discovered, spectroscopically by Sir William Crookes at 1861 in England. The element was named after the green spectral line, which identified the element (from the Greek word "thallos" meaning "green twig" or green shoot). The metal was isolated both by Crookes and Lamy in 1862. They had been expecting to isolate tellurium after removing selenium from the byproducts from a commercial sulphuric acid factory but instead foundthe new element thallium.

Physical properties 
•Melting point: 577 [or 304 °C (579 °F)] K
•Boiling point: 1746 [or 1473 °C (2683 °F)] K
•Density of solid: 11850 kg m-3

Orbital properties
•Ground state electron configuration: [Xe].4f14.5d10.6s2.6p1
•Shell structure: 2.8.18.32.18.3
•Term symbol: 2P1/2

Isolation
Thallium metal would not normally be made in the laboratory as it is available commercially. Crude thallium is present as a component in flue dust along with arsenic, cadmium, indium, germanium, lead, nickel, selenium, tellurium, and zinc. This is done by dissolving in dilute acid, precipitating out lead sulphate, and then adding HCl to precipitate thallium chloride, TlCl. Further purification can be achieved by electrolysis of soluble thallium salts.

 

Thursday, December 26, 2013

Mercury (80)


MERCURY (a.k.a. Quicksilver!)

Mercury is the only common metal liquid at ordinary temperatures. Mercury is sometimes called quicksilver. It rarely occurs free in nature and is found mainly in cinnabar ore (HgS) in Spain and Italy. It is a heavy, silvery-white liquid metal. It is a rather poor conductor of heat as compared with other metals but is a fair conductor of electricity. It alloys easily with many metals, such as gold, silver, and tin. These alloys are called amalgams. Its ease in amalgamating with gold is made use of in the recovery of gold from its ores.

•Name: Mercury
•Symbol: Hg
•Atomic number: 80
•Atomic weight: 200.59 (2) 
•Standard state: liquid at 298 K (the heaviest known elemental liquid)
•CAS Registry ID: 7439-97-6
•Group in periodic table: 12
•Group name: (none)
•Period in periodic table: 6 
•Block in periodic table: d-block
•Color: silvery white
•Classification: Metallic

Historical information
Mercury has been known since ancient times, and the discoverer is not known. Origin of name: named after the planet "Mercury" (the origin of the symbol Hg is the Latin word "hydrargyrum" meaning "liquid silver").Mercury was known to ancient Chinese and Hindus before 2000 BC and was found in tubes in Egyptian tombs dated from 1500 BC It was used to forma amalgams of other metals around 500 BC. The Greeks used mercury in ointments and the Romans used it, unfortunately for those using it, in cosmetics.

Mercury is one of the elements which has an alchemical symbol, being a semicircle sitting atop a circle, atop a short legged cross. Or, the symbol for female with a semicircle on top.

The most important salts are mercuric chloride HgC12 (corrosive sublimate - a violent poison), mercurous chloride Hg2Cl2 (calomel, occasionally still used in medicine), mercury fulminate (Hg(ONC)2, a detonator used in explosives), and mercuric sulphide (HgS, vermillion, a high-grade paint pigment). 

Organic mercury compounds are important - and dangerous. Methyl mercury is a lethal pollutant found in rivers and lakes. The main source of pollution is industrial wastes settling to the river and lake bottoms.

As mercury is a very volatile element, dangerous levels are readily attained in air. Mercury vapour should not exceed 0.1 mg m-3 in air. Air saturated with the vapour at 20°C contains mercury in a concentration far greater than that limit. The danger increases at higher temperatures. It is therefore important that mercury be handled with care. Containers of mercury should be securely covered and spillage should be avoided. Mercury should only be handled under in a well-ventilated area. If you are in possession of any mercury you are advised to contact a properly qualified chemist or public health laboratory for its safe disposal.

 

Monday, December 23, 2013

Gold (79)


AUREM....or GOLD, if you prefer!

Most metals are metallic grey or silvery white whereas gold is characteristically a metallic yellow colour, in other words gold-coloured. Cesium is also gold coloured. The gold colour seems related to relativistic effects of the outermost gold orbitals. 

Small amounts of other metals alloyed with gold change the colour as well as mechanical properties such as hardness. White gold for jewelry is formed by mixing palladium, silver, or nickel with gold, although the result is green gold with certain proportions of silver. White gold is commonly used for wedding rings in the USA. Addition of some copper gives "rose gold", a soft pink colour. Remarkably other colours such as purple (a gold:aluminium alloy), blue (a gold:indium alloy) and even black (a gold:cobalt alloy) may be formed. 

Gold is usually alloyed in jewellery to give it more strength, and the term carat describes the amount of gold present (24 carats is pure gold). It is estimated that all the gold in the world, so far refined, could be placed in a single cube 60 ft. on a side. It is metallic, with a yellow colour when in a mass, but when finely divided it may be black, ruby, or purple. 

It is the most malleable and ductile metal; 1 ounce (28 g) of gold can be beaten out to 300 square feet. It is a soft metal and is usually alloyed to give it more strength. It is a good conductor of heat and electricity, and is unaffected by air and most reagents.

Gold is readily available commercially and its price (see the UtiliseGold directory if you wish to track it) changes day by day and is one of the most widely tracked commercial prices.

The most common gold compounds are auric chloride (AuCl3) and chlorauric acid (HAuCl4). A mixture of one part nitric acid with three of hydrochloric acid is called aqua regia (because it dissolved gold, the King of Metals). It is unaffected by air and most reagents. It is found free in nature and associated with quartz, pyrite and other minerals. Two thirds of the world's supply comes from South Africa, and 2/3 of USA production is from South Dakota and Nevada. Gold is found in sea water, but no effective economic process has been designed (yet) to extract it from this source.

•Name: Gold
•Symbol: Au
•Atomic number: 79
•Atomic weight: 196.966569 (4) 
•Standard state: solid at 298 K
•CAS Registry ID: 7440-57-5
•Group in periodic table: 11
•Group name: Coinage metal
•Period in periodic table: 6 
•Block in periodic table: d-block
•Color: yellow colored; gold
•Classification: Metallic

Historical information
Gold had been known since the ancient times, and I couldn't find a specific discoverer. Origin of name is from the Anglo-Saxon word "gold" (the origin of the symbol Au is the Latin word "aurum" meaning "gold"). Gold has always fascinated people and gold is certainly one of the very first metals known. Nobody knows who picked up a gold nugget first but it would have been because it was shiny. Gold was highly valued from from the earliest recorded times in history. It seems that the Egyptians developed gold smelting some 5600 years ago (about 3600 BC) using clay blowpipes to heat the smelter contents. Egyption inscriptions dating back to 2600 BC describe gold. Gold workers from Mesopotamia (known now as Iraq) made one of the earliest known pieces of gold jewellery in about 2600 BC. Gold is mentioned several times in the Old Testament. Tutankhamun's funeral mask is one of the most iconic gold pieces known. It was made around 1223 BC and is a stunning piece of ancient gold craftsmanship.

The first use of gold in dentistry as the Etruscans (an ancient Italian civilisation from an area corresponding now to Tuscany) begin securing substitute teeth with gold wire, and with astonishing skill. This was as early as 700-600 BC. Apparently Etruscan craftsmen made gold dental bridges for women so that they could show display their wealth and status. Some women had their incisors removed so that they could be fitted with the gold prosthetics. The Etruscans probably learned dentistry from the Egyptians, Phoenicians, and Greeks but took the art much further. Many specimens of Etruscan dental fittings are to be found in Italian and other museums.

Gold loops were fitted over the remaining natural teeth, set in place, and maintained by solder. The patient's missing teeth were replaced by either the teeth of human beings and on occasion the tooth of an ox.

Bio-compatibility, malleability and corrosion resistance make gold valuable even today in dental applications, and is often used as a chelating agent for treatments in some autoimmune diseases, like rheumatoid arthritis.

Colloidal gold has been used since Roman times to colour glass shades of yellow, red, or violet. Melting gold powder into glass diffuses gold nanoparticles into the glass, these refract light, giving the glass a luminous red glow. THe precise colour depends upon the form of the colloidal gold. Faraday (1857) recognised that the colour is due to the minute size of the gold particles and called the sample he made 'activated gold'. In 1898 Richard Adolf Zsigmondy prepared the first colloidal gold in dilute solution. Today, colloidal gold is made by the addition of reducing agents to dilute solutions of Au(III) (the auric ion). One famous form is that made by the use of tin dichloride (SnCl2) as reducing agent. This is a very stable form of colloidal gold and is known as the "Purple of Cassius". It is suitable for colouring ceramics and glasses, and in addition is a good test for Au(III). The form that Faraday studied was made using phosphorus to reduce gold chloride.

Gold is one of the elements which has an alchemical symbol, a circle with a dot in the center.

Hallmarking practice established The world's first "hallmarking" system was established at Goldsmith's Hall in London in 1300 AD. London's Assay Office is still there. THe purpose of the hallmarking system is to determine and guarantee the quality of precious metals such as gold.

Sometime prior to the autumn of 1803, the Englishman John Dalton was able to explain the results of some of his studies by assuming that matter is composed of atoms and that all samples of any given compound consist of the same combination of these atoms. Dalton also noted that in series of compounds, the ratios of the masses of the second element that combine with a given weight of the first element can be reduced to small whole numbers (the law of multiple proportions). This was further evidence for atoms. Dalton's theory of atoms was published by Thomas Thomson in the 3rd edition of his System of Chemistry in 1807 and in a paper about strontium oxalates published in the Philosophical Transactions. Dalton published these ideas himself in the following year in the New System of Chemical Philosophy. 

Gold has been the basis of many currencies over the centuries and so for economic reasons, among others, the possession of gold was or is restricted in some countries. Notably, private ownership of gold (apart from as jewellery and coins) was banned between 1933 and 1975. In 1422 the Venice Mint made ("struck") 1.2 million gold ducats using 4.26 metric tonnes of gold. These small coins (each about 3.5 g) were popular perhaps because they were easy to make and are highly transportable. In 1717 Great Britain moved to a pure gold standard. The British government linked the currency to gold at a fixed rate (77 shillings, ten and a half pennies per ounce of gold).

The Californian Gold Rush of 1848 and 1855 started on 24 January 1848 when gold was found by James W. Marshall at Sutter's Mill, in Coloma, California. Although attempts were made to keep the discovery quiet, news leaked out and the result was the migration of 300,000 people to California from the United States and beyond. The New York Herald was the first East Coast newspaper to report the discovery of gold and on 5 December 1848, President James Polk confirmed the discovery in an address to Congress. The gold-seekers were called the "Forty-niners" and often had a very hard time. Prospectors retrieved the gold from streams and riverbeds using low-technology methods such as panning. More sophisticated methods of gold recovery were eventually developed. Gold worth tens of billions of US dollars (2010 equivalent price) was extracted. Some became wealthy but many finished with little profit and a lot of heartache. Today, the forty-niners name lives on in the name of the San Francisco 49ers, an American football team in California. 

Some years later in 1885 the South African Gold Rush began. An Australian miner, George Harrison, found gold on Langlaagte farm near Johannesburg while digging to build a house. South Africa became the source of almost one-half of the world's gold.

 

Thursday, December 19, 2013

Platinum (78)


Ruthenium, rhodium, palladium, osmium, iridium, and platinum together make up a group of elements referred to as the platinum group metals (PGM).

Platinum is a beautiful silvery-white metal, when pure, and is malleable and ductile. It has a coefficient of expansion almost equal to that of soda-lime-silica glass, and is therefore used to make sealed electrodes in glass systems.

The metal does not oxidise in air. It is insoluble in hydrochloric and nitric acid, but dissolves when they are mixed as aqua regia, forming chloroplatinic acid (H2PtCl6), an important compound. It is corroded by halogens, cyanides, sulphur and alkalis. Hydrogen and oxygen gas mixtures explode in the presence of platinum wire.

•Name: Platinum
•Symbol: Pt
•Atomic number: 78
•Atomic weight: 195.084 (9) 
•Standard state: solid at 298 K
•CAS Registry ID: 7440-06-4
•Group in periodic table: 10
•Group name: Precious metal or platinum group metal
•Period in periodic table: 6 
•Block in periodic table: d-block
•Color: greyish white
•Classification: Metallic

Historical information
Platinum was discovered by Antonio de Ulloa at 1735 in South America. Origin of name: from the Spanish word "platina" meaning "silver". The metal was used by pre-Columbian Indians but platinum was "rediscovered" in South America by Ulloa in 1735 and by Wood in 1741. In 1822 plenty of platinum was discovered in the Ural Mountains in Russia.

Platinum is one of the elements which has an alchemical symbol, a left facing crescent attached to a circle with a dot in the center.

Sometime prior to the autumn of 1803, the Englishman John Dalton was able to explain the results of some of his studies by assuming that matter is composed of atoms and that all samples of any given compound consist of the same combination of these atoms. Dalton also noted that in series of compounds, the ratios of the masses of the second element that combine with a given weight of the first element can be reduced to small whole numbers (the law of multiple proportions). This was further evidence for atoms. Dalton's theory of atoms was published by Thomas Thomson in the 3rd edition of his System of Chemistry in 1807 and in a paper about strontium oxalates published in the Philosophical Transactions. Dalton published these ideas himself in the following year in the New System of Chemical Philosophy. The symbol used by Dalton for platinum is a circle with a capital P in the center.

Physical properties 
•Melting point: 2041.4 [or 1768.3 °C (3214.9 °F)] K
•Boiling point: 4098 [or 3825 °C (6917 °F)] K
•Density of solid: 21090 kg m-3

Orbital properties
•Ground state electron configuration: [Xe].4f14.5d9.6s1
•Shell structure: 2.8.18.32.17.1
•Term symbol: 3D3

Isolation
It would not normally be necessary to make a sample of platinum in the laboratory as the metal is available commercially. The industrial extraction of platinum is complex as the metal occurs in ores mixed with other metals such as palladium and gold. Sometimes extraction of the precious metals such as platinum and palladium is the main focus of a partiular industrial operation while in other cases it is a byproduct. The extraction is complex and only worthwhile since platinum is the basis of important catalysts in industry.

Preliminary treatment of the ore or base metal byproduct with aqua regia (a mixture of hydrochloric acid, HCl, and nitric acid, HNO3) gives a solution containing complexes of gold and palladium as well as H2PtCl6. The gold is removed from this solution as a precipitate by treatment with iron chloride (FeCl2). The platinum is precipitated out as impure (NH4)2PtCl6 on treatment with NH4Cl, leaving H2PdCl4 in solution. The (NH4)2PtCl6 is burned to leave an impure platinum sponge. This can be purified by redissolving in aqua regia, removal of rhodium and iridium impurities by treatment of the solution with sdoium bromate, and precipitation of pure (NH4)2PtCl6 by treatment with ammonium hydroxide, NH4OH. This yields platinum metal by burning.


 

Monday, December 16, 2013

Iridium (77)


Ruthenium, rhodium, palladium, osmium, iridium, and platinum together make up a group of elements referred to as the platinum group metals (PGM).

The name iridium is appropriate, for its salts are highly coloured. Iridium is white, similar to platinum, but with a slight yellowish cast. It is very hard and brittle, making it very hard to machine, form, or work. It is the most corrosion resistant metal known, and was used in making the standard metre bar of Paris, which is a 90% platinum-10% iridium alloy. This meter bar has since been replaced as a fundamental unit of length. 

Iridium is not attacked by any of the acids nor by aqua regia, but is attacked by molten salts, such as NaCl and NaCN.

•Name: Iridium
•Symbol: Ir
•Atomic number: 77
•Atomic weight: 192.217 (3) 
•Standard state: solid at 298 K
•CAS Registry ID: 7439-88-5
•Group in periodic table: 9
•Group name: Precious metal or Platinum group metal
•Period in periodic table: 6 
•Block in periodic table: d-block
•Color: silvery white
•Classification: Metallic

Historical information
Iridium was discovered by Smithson Tennant, Antoine Fourcroy, Louis Vanquelin, Hippolyte Collet-Descotils at 1803 in England, France. Origin of name: from the Greek word "iris" meaning "rainbow". Osmium was discovered in 1803 by Smithson Tennant in the dark coloured residue left when crude platinum is dissolved by aqua regia (a mixture of hydrochloric and nitric acid). This dark residue contains both osmium and iridium (named after the Latin word iris meaning rainbow because of the colourful nature of iridium compounds).

Physical properties 
•Melting point: 2739 [or 2466 °C (4471 °F)] K
•Boiling point: 4701 [or 4428 °C (8002 °F)] K
•Density of solid: 22650 kg m-3

Orbital properties
•Ground state electron configuration: [Xe].4f14.5d7.6s2
•Shell structure: 2.8.18.32.15.2
•Term symbol: 4F9/2

Isolation
It would not normally be necessary to make a sample of iridium in the laboratory as the metal is available, at a price, commercially. The industrial extraction of iridium is complex as the metal occurs in ores mixed with other metals such as rhodium, palladium, silver, platinum, and gold. Sometimes extraction of the precious metals such as iridium, rhodium, platinum and palladium is the main focus of a partiular industrial operation while in other cases it is a byproduct. The extraction is complex because of the other metals present and only worthwhile since iridium is useful as a specialist metal and is the basis of some catalysts in industry.

Preliminary treatment of the ore or base metal byproduct is required to remove silver, gold, palladium, and platinum. The residue is melted with sodium bisulphate (NaHSO4) and the resulting mixture extracted with water to give a solution containing rhodium sulphate, Rh2(SO4)3. The insoluble residue contains the iridium. The residue is melted with Na2O2 and extracted into water to remove ruthenium and osmium salts. The residue contains iridium oxide, IrO2. Dissolution of the oxide in regia (a mixture of hydrochloric acid, HCl, and nitric acid, HNO3) gives a solution containing pure (NH4)3IrCl6. Evaporation to dryness and burning under hydrogen gas gives pure iridium.


 

Thursday, December 12, 2013

Osmium (76)

OSMIUM (no - nothing to do with Oscorp or the wonderful wizard):

Ruthenium, rhodium, palladium, osmium, iridium, and platinum together make up a group of elements referred to as the platinum group metals (PGM).

Osmium metal is lustrous, bluish white, extremely hard, and brittle even at high temperatures. It has the highest melting point and lowest vapour pressure of the platinum group. The metal is very difficult to fabricate, but the powder can be sintered in a hydrogen atmosphere at a temperature of 2000°C. The solid metal is not affected by air at room temperature, but the powdered or spongy metal slowly gives off osmium tetroxide, which is a powerful oxidising agent and has a strong smell. The tetroxide is highly toxic, and boils at 130°C (760 mm). Concentrations in air as low as 10-7 g m-3 can cause lung congestion, skin damage, or eye damage.

•Name: Osmium
•Symbol: Os
•Atomic number: 76
•Atomic weight: 190.23 (3) [see note g]
•Standard state: solid at 298 K
•CAS Registry ID: 7440-04-2
•Group in periodic table: 8
•Group name: Precious metal or Platinum group metal
•Period in periodic table: 6 
•Block in periodic table: d-block
•Colour: bluish grey
•Classification: Metallic

Historical information
Osmium was discovered by Smithson Tennant at 1803 in England, in the dark coloured residue left when crude platinum is dissolved by aqua regia (a mixture of hydrochloric and nitric acid). This dark residue contains both osmium (named after osme meaning odour) and iridium. Origin of name is from the Greek word "osme" meaning "smell".

Physical properties 
•Melting point: 3306 [or 3033 °C (5491 °F)] K
•Boiling point: 5285 [or 5012 °C (9054 °F)] K
•Density of solid: 22610 kg m-3

Orbital properties
•Ground state electron configuration: [Xe].4f14.5d6.6s2
•Shell structure: 2.8.18.32.14.2
•Term symbol: 5D4

Isolation
It would not normally be necessary to make a sample of osmium in the laboratory as the metal is available, at a price, commercially. The industrial extraction of osmium is complex as the metal occurs in ores mixed with other metals such as ruthenium, rhodium, palladium, silver, platinum, and gold. Sometimes extraction of the precious metals such as iridium, rhodium, platinum and palladium is the main focus of a partiular industrial operation while in other cases it is a byproduct. The extraction is complex because of the other metals present and only worthwhile since osmium is useful as a specialist metal and is the basis of some catalysts in industry.

Preliminary treatment of the ore or base metal byproduct is required to remove silver, gold, palladium, and platinum. The residue is melted with sodium bisulphate (NaHSO4) and the resulting mixture extracted with water to give a solution containing rhodium sulphate, Rh2(SO4)3. The insoluble residue contains the osmium. The residue is melted with Na2O2 and extracted into water to extract the ruthenium and osmium salts (including [RuO4]2- and [OsO4(OH)2]2-). The residue contains iridium oxide, IrO2. Reaction of the salt with chlorine gas gives the volatile oxides RuO4 and OsO4. The osmium oxide is dissolved by treatment with alcoholic sodium hydroxide to form Na2[OsO2(OH)4], and the osmium precipiated out as pure OsCl2O2(NH3)4 by treatment with NH4Cl. Evaporation to dryness and burning under hydrogen gas gives pure osmium.


 

Monday, December 9, 2013

Rhenium (75)


Rhenium is silvery white with a metallic lustre; its density is exceeded only by that of platinum, iridium, and osmium, and its melting point is exceeded only by that of tungsten and carbon. It has other useful properties. It is expensive but useful as a trace alloying agent.

Table: basic information about and classifications of rhenium. •Name: Rhenium
•Symbol: Re
•Atomic number: 75
•Atomic weight: 186.207 (1) 
•Standard state: solid at 298 K
•CAS Registry ID: 7440-15-5
•Group in periodic table: 7
•Group name: (none)
•Period in periodic table: 6 
•Block in periodic table: d-block
•Colour: greyish white
•Classification: Metallic

Historical information
Rhenium was discovered by Walter Noddack, Ida Tacke, and Otto Berg at 1925 in Germany, who announced that they had detected the element in platinum ores and columbite. Origin of name is from the Greek word "Rhenus" meaning river "Rhine". 

Physical properties 
•Melting point: 3459 [or 3186 °C (5767 °F)] K
•Boiling point: 5869 [or 5596 °C (10105 °F)] K
•Density of solid: 21020 kg m-3

Orbital properties
•Ground state electron configuration: [Xe].4f14.5d5.6s2
•Shell structure: 2.8.18.32.13.2
•Term symbol: 6S5/2

Isolation
Commercial rhenium is extracted from molybdenum roaster-flue gas obtained from copper-sulfide ores. Some molybdenum ores contain 0.001% to 0.2% rhenium. Rhenium(VII) oxide and perrhenic acid readily dissolve in water; they are leached from flue dusts and gasses and extracted by precipitating with potassium or ammonium chloride as the perrhenate salts, and purified by recrystallization. Total world production is between 40 and 50 tons/year; the main producers are in Chile, the United States, Peru, and Poland. Recycling of used Pt-Re catalyst and special alloys allow the recovery of another 10 tons per year. Prices for the metal rose rapidly in early 2008, from $1000–$2000 per kg in 2003–2006 to over $10,000 in February 2008. The metal form is prepared by reducing ammonium perrhenate with hydrogen at high temperatures:

2 NH4ReO4 + 7 H2 → 2 Re + 8 H2O + 2 NH3


 

Thursday, December 5, 2013

Tungsten (74)


Pure tungsten is a steel-gray to tin-white metal. Tungsten has the highest melting point and lowest vapour pressure of all metals, and at temperatures over 1650°C has the highest tensile strength. The metal oxidises in air and must be protected at elevated temperatures. It has excellent corrosion resistance and is attacked only slightly by most mineral acids.

•Name: Tungsten
•Symbol: W
•Atomic number: 74
•Atomic weight: 183.84 (1) 
•Standard state: solid at 298 K
•CAS Registry ID: 7440-33-7
•Group in periodic table: 6
•Group name: (none)
•Period in periodic table: 6 
•Block in periodic table: d-block
•Color: greyish white, lustrous
•Classification: Metallic


Historical information
Tungsten was discovered by Fausto and Juan Jose de Elhuyar at 1783 in Spain. Origin of name is from the Swedish words "tung sten" meaning "heavy stone" (the origin of the symbol W is "wolfram ", named after the tungsten mineral wolframite). Tungsten used to be known as wolfram, from wolframite, said to be named from wolf rahm or spumi lupi, because the ore interfered with the smelting of tin and was supposed to devour the tin. The de Elhuyar brothers found an acid in wolframite in 1783 that they succeeded in reducing to the elemental metal with charcoal. 

Physical properties 
•Melting point: 3695 [or 3422 °C (6192 °F)] K
•Boiling point: 5828 [or 5555 °C (10031 °F)] K
•Density of solid: 19250 kg m-3

Orbital properties
•Ground state electron configuration: [Xe].4f14.5d4.6s2
•Shell structure: 2.8.18.32.12.2
•Term symbol: 5D0

Tungsten Uses: 
The thermal expansion of tungsten is similar to that of borosilicate glass, so the metal is used for glass/metal seals. 
Tungsten and its alloys are used to make filaments for electric lamps and television tubes, as electrical contacts, x-ray targets, heating elements, for metal evaporation components, and for numerous other high temperature applications. 
Hastelloy, Stellite, high-speed tool steel, and numerous other alloys contain tungsten. Magnesium and calcium tungstenates are used in fluorescent lighting. 
Tungsten carbide is important in the mining, metalworking, and petroleum industries. Tungsten disulfide is used as a dry high-temperature lubricant. 
Tungsten bronze and other tungsten compounds are used in paints.

Tungsten has the highest melting point of any metal at 3,410 Deg. C 
Tungsten is popular in jewelry making because of its durability
Used for making different light bulbs 

Tungsten Sources: 
Tungsten occurs in wolframite, (Fe, Mn)WO4, scheelite, CaWO4, ferberite, FeWO4, and huebnerite, MnWO4. Tungsten is produced commercially by reducing tungsten oxide with carbon or hydrogen.


 

Monday, December 2, 2013

Tantalum (73)


Tantalum is a greyish silver, heavy, and very hard metal. When pure, it is ductile and can be drawn into fine wire, which can be used as a filament for evaporating metals such as aluminium. Tantalum is almost completely immune to chemical attack at temperatures below 150°C, and is attacked only by hydrofluoric acid, acidic solutions containing the fluoride ion, and free sulphur trioxide. The element has a melting point exceeded only by tungsten and rhenium.

Table: basic information about and classifications of tantalum.
•Name: Tantalum
•Symbol: Ta
•Atomic number: 73
•Atomic weight: 180.94788 (2) 
•Standard state: solid at 298 K
•CAS Registry ID: 7440-25-7
•Group in periodic table: 5
•Group name: (none)
•Period in periodic table: 6 
•Block in periodic table: d-block
•Color: grey blue
•Classification: Metallic

Historical information
Tantalum was discovered by Anders Gustaf Ekeberg at 1802 in Sweden, but many chemists thought niobium and tantalum were one and the same. Origin of name is from the Greek word "Tantalos" meaning "father of Niobe" (Greek mythology: According to Homer’s Iliad, she had six sons and six daughters and boasted of her progenitive superiority to the Titan Leto, who had only two children, the twin deities Apollo and Artemis. As punishment for her pride, Apollo killed all Niobe’s sons, and Artemis killed all her daughters Oh how pleasant those gods and goddesses...). Tantalum is closely related to niobium in the periodic table, so the names are fitting! Some felt that perhaps tantalum was an allotrope [coined from Greek words meaning "other" + "form") is the property of some chemical elements to exist in two or more different forms] of niobium. Later, Rose, in 1844, and Marignac, in 1866, showed that niobic and tantalic acids were two different acids.

The first relatively pure tantalum was produced by von Bolton in 1907. 

Physical properties 
•Melting point: 3290 [or 3017 °C (5463 °F)] K
•Boiling point: 5731 [or 5458 °C (9856 °F)] K
•Density of solid: 16650 kg m-3

Orbital properties
•Ground state electron configuration: [Xe].4f14.5d3.6s2
•Shell structure: 2.8.18.32.11.2
•Term symbol: 4F3/2

Isolation
Isolation of tantalum appears to be complicated. Tantalum minerals usually contain both niobium and tantalum. Since they are so similar chemically, it is difficult to separate them. Tantalum can be extracted from the ores by first fusing the ore with alkali, and then extracting the resultant mixture into hydrofluoric acid, HF. Current methodology involves the separation of tantalum from these acid solutions using a liquid-liquid extraction technique. In this process tantalum salts are extracted into the ketone MIBK (methyl isobutyl ketone, 4-methyl pentan-2-one). The niobium remains in the HF solution. 

After conversion to the oxide, metallic tantalum can be made by reduction with sodium or carbon. Electrolysis of molten fluorides is also used.

 

Thursday, November 28, 2013

Hafnium (72)



Most zirconium minerals contain 1 to 3% hafnium. Hafnium is a ductile metal with a brilliant silver lustre. Its properties are influenced considerably by the impurities of zirconium present. Of all the elements, zirconium and hafnium are two of the most difficult to separate. Hafnium is a Group 4 transition element.

Because hafnium has a good absorption cross section for thermal neutrons (almost 600 times that of zirconium), has excellent mechanical properties, and is extremely corrosion resistant, it is used for nuclear reactor control rods.

Hafnium carbide is the most refractory binary composition known, and the nitride is the most refractory metal nitride (m.p. 3310°C).

•Name: Hafnium
•Symbol: Hf
•Atomic number: 72
•Atomic weight: 178.49 (2) 
•Standard state: solid at 298 K
•CAS Registry ID: 7440-58-6
•Group in periodic table: 4
•Group name: (none)
•Period in periodic table: 6 
•Block in periodic table: d-block
•Color: grey steel
•Classification: Metallic

Historical information
Hafnium was discovered by Dirk Coster and George Charles von Hevesy at 1923 in Denmark, though it was thought to be present in various zirconium minerals many years prior to its discovery. Origin of name is from the Latin name "Hafnia" meaning "Copenhagen." It was finally identified in zircon (a zirconium ore) from Norway, by means of X-ray spectroscopic analysis. It was named in honour of the city in which the discovery was made. A number of earlier claims seem less likely.

Most zirconium minerals contain 1 to 3% hafnium and it is their chemical similarity which made their separation difficult. It was originally separated from zirconium by repeated and tedious recrystallization of the double ammonium or potassium fluorides.

Physical properties 
•Melting point: 2506 [or 2233 °C (4051 °F)] K
•Boiling point: 4876 [or 4603 °C (8317 °F)] K
•Density of solid: 13310 kg m-3

Orbital properties
•Ground state electron configuration: [Xe].4f14.5d2.6s2
•Shell structure: 2.8.18.32.10.2
•Term symbol: 3F2

Isolation
Isolation: hafnium extraction is always associated with its removal from zirconium as it is a contaminant of all zirconium minerals. Solvent extraction methods are used ot spearate the two metals but the process is not easy. These make use of the differential solubilities of the metal thiocyantes (thiocyanate is SCN-) in methyl isobutyl ketone.


 

Monday, November 25, 2013

Lutetium (71)


Pure metallic lutetium has been isolated only in recent years and is one of the more difficult to prepare. It can be prepared by the reduction of anhydrous LuCl3 or LuF3 by an alkali or alkaline earth metal.

The metal is silvery white and relatively stable in air. It is a rare earth metal and perhaps the most expensive of all rare elements. It is found in small amounts with all rare earth metals, and is very difficult to separate from other rare elements.

•Name: Lutetium
•Symbol: Lu
•Atomic number: 71
•Atomic weight: 174.9668
•Standard state: solid at 298 K
•CAS Registry ID: 7439-94-3
•Group in periodic table: 3
•Group name: (none)
•Period in periodic table: 6 
•Block in periodic table: d-block
•Color: silvery white
•Classification: Metallic

Hstorical information
Lutetium was discovered by Georges Urbain in France and Carl Auer von Welsbach at 1907 in France, around the same time and independently. Origin of name is from the Greek word "Lutetia" meaning "Paris". In 1907, Georges Urbain described a process by which Marignac's ytterbium (1879) could be separated into the two elements, ytterbium (neoytterbium) and lutetium. These elements were identical with "aldebaranium" and "cassiopeium", independently discovered by von Welsbach at about the same time. 

Physical properties 
•Melting point: 1925 [or 1652 °C (3006 °F)] K
•Boiling point: 3675 [or 3402 °C (6156 °F)] K
•Density of solid: 9841 kg m-3

Orbital properties
•Ground state electron configuration: [Xe].4f14.5d1.6s2
•Shell structure: 2.8.18.32.9.2
•Term symbol: 2D3/2

Isolation
Lutetium metal is available commercially so it is not normally necessary to make it in the laboratory, which is just as well as it is difficult to isolate as the pure metal. This is largely because of the way it is found in nature. The lanthanoids are found in nature in a number of minerals. The most important are xenotime, monazite, and bastnaesite. The first two are orthophosphate minerals LnPO4 (Ln deonotes a mixture of all the lanthanoids except promethium which is vanishingly rare) and the third is a fluoride carbonate LnCO3F. Lanthanoids with even atomic numbers are more common. The most comon lanthanoids in these minerals are, in order, cerium, lanthanum, neodymium, and praseodymium. Monazite also contains thorium and ytrrium which makes handling difficult since thorium and its decomposition products are radioactive.

For many purposes it is not particularly necessary to separate the metals, but if separation into individual metals is required, the process is complex. Initially, the metals are extracted as salts from the ores by extraction with sulphuric acid (H2SO4), hydrochloric acid (HCl), and sodium hydroxide (NaOH). Modern purification techniques for these lanthanoid salt mixtures are ingenious and involve selective complexation techniques, solvent extractions, and ion exchange chromatography. 

Pure lutetium is available through the reduction of LuF3 with calcium metal.

2LuF3 + 3Ca → 2Lu + 3CaF2

This would work for the other calcium halides as well but the product CaF2 is easier to handle under the reaction conditions (heat to 50°C above the melting point of the element in an argon atmosphere). Excess calcium is removed from the reaction mixture under vacuum.


 

Thursday, November 21, 2013

Ytterbium (70)


Ytterbium has a bright silvery lustre, is soft, malleable, and quite ductile. While the element is fairly stable, it should be kept in closed containers to protect it from air and moisture. Ytterbium is readily attacked and dissolved by mineral acids and reacts slowly with water.

•Name: Ytterbium
•Symbol: Yb
•Atomic number: 70
•Atomic weight: 173.054 (5) [see note g]
•Standard state: solid at 298 K
•CAS Registry ID: 7440-64-4
•Group in periodic table: 
•Group name: Lanthanoid
•Period in periodic table: 6 (lanthanoid)
•Block in periodic table: f-block
•Colour: silvery white
•Clasification: Metallic

Historical information
Ytterbium was discovered by Jean de Marignac at 1878 in Switzerland, which he named after the village of "Ytterby" near Vaxholm in Sweden. In 1878 Marignac discovered a component, which he called ytterbia, in the earth then known as erbia. In 1907, Urbain separated ytterbia into two components, which he called neoytterbia and lutecia. The elements in these earths are now known as ytterbium and lutetium, respectively. These elements are identical with aldebaranium and cassiopeium, discovered independently and at about the same time by von Welsbach. The impure element was first prepared by Klemm and Bonner in 1937 who reduced ytterbium trichloride with potassium. Daane, Dennison, and Spedding prepared a purer form in 1953 from which the chemical and physical properties of the element could be determined.

Physical properties 
•Melting point: 1097 [or 824 °C (1515 °F)] K
•Boiling point: 1469 [or 1196 °C (2185 °F)] K
•Density of solid: 6570 kg m-3

Orbital properties
•Ground state electron configuration: [Xe].4f14.6s2
•Shell structure: 2.8.18.32.8.2
•Term symbol: 1S0

Isolation
Ytterbium metal is available commercially so it is not normally necessary to make it in the laboratory, which is just as well as it is difficult to isolate as the pure metal. This is largely because of the way it is found in nature. The lanthanoids are found in nature in a number of minerals. The most important are xenotime, monazite, and bastnaesite. The first two are orthophosphate minerals LnPO4 (Ln deonotes a mixture of all the lanthanoids except promethium which is vanishingly rare) and the third is a fluoride carbonate LnCO3F. Lanthanoids with even atomic numbers are more common. The most comon lanthanoids in these minerals are, in order, cerium, lanthanum, neodymium, and praseodymium. Monazite also contains thorium and ytrrium which makes handling difficult since thorium and its decomposition products are radioactive.

For many purposes it is not particularly necessary to separate the metals, but if separation into individual metals is required, the process is complex. Initially, the metals are extracted as salts from the ores by extraction with sulphuric acid (H2SO4), hydrochloric acid (HCl), and sodium hydroxide (NaOH). Modern purification techniques for these lanthanoid salt mixtures are ingenious and involve selective complexation techniques, solvent extractions, and ion exchange chromatography. 

Pure ytterbium is available through the electrolysis of a mixture of molten YbCl3 and NaCl (or CaCl2) in a graphite cell which acts as cathode using graphite as anode. The other product is chlorine gas.

Monday, November 18, 2013

Thulium (69)


Thulium is the least abundant of the earth elements, and is about as rare as silver, gold, or cadmium.

The pure metal has a bright, silvery lustre. It is reasonably stable in air, but the metal must be protected from moisture. The element is silvery-grey, soft, malleable, and ductile, and can be cut with a knife. It is a rare earth metal found in minerals such as monazite.

•Name: Thulium
•Symbol: Tm
•Atomic number: 69
•Atomic weight: 168.93421 (2) 
•Standard state: solid at 298 K
•CAS Registry ID: 7440-30-4
•Group in periodic table: 
•Group name: Lanthanoid
•Period in periodic table: 6 (lanthanoid)
•Block in periodic table: f-block
•Color: silvery white
•Classification: Metallic

Historical information
Thulium was discovered by Per Theodore Cleve at 1879 in Sweden, while working on erbia earth (erbium oxide). Origin of name: named after ""Thule", an ancient name for Scandinavia. Thulium oxide (holmia) was present as an impurity in the erbia. The element is named after Thule, the ancient name for Scandinavia. 

Physical properties 
•Melting point: 1818 [or 1545 °C (2813 °F)] K
•Boiling point: 2223 [or 1950 °C (3542 °F)] K
•Density of solid: 9321 kg m-3

Orbital properties
•Ground state electron configuration: [Xe].4f13.6s2
•Shell structure: 2.8.18.31.8.2
•Term symbol: 2F7/2

Isolation
Thulium metal is available commercially so it is not normally necessary to make it in the laboratory, which is just as well as it is difficult to isolate as the pure metal. This is largely because of the way it is found in nature. The lanthanoids are found in nature in a number of minerals. The most important are xenotime, monazite, and bastnaesite. The first two are orthophosphate minerals LnPO4 (Ln deonotes a mixture of all the lanthanoids except promethium which is vanishingly rare) and the third is a fluoride carbonate LnCO3F. Lanthanoids with even atomic numbers are more common. The most comon lanthanoids in these minerals are, in order, cerium, lanthanum, neodymium, and praseodymium. Monazite also contains thorium and ytrrium which makes handling difficult since thorium and its decomposition products are radioactive.

For many purposes it is not particularly necessary to separate the metals, but if separation into individual metals is required, the process is complex. Initially, the metals are extracted as salts from the ores by extraction with sulphuric acid (H2SO4), hydrochloric acid (HCl), and sodium hydroxide (NaOH). Modern purification techniques for these lanthanoid salt mixtures are ingenious and involve selective complexation techniques, solvent extractions, and ion exchange chromatography. 

Pure thulium is available through the reduction of TmF3 with calcium metal.

2TmF3 + 3Ca → 2Tm + 3CaF2

This would work for the other calcium halides as well but the product CaF2 is easier to handle under the reaction conditions (heat to 50°C above the melting point of the element in an argon atmosphere). Excess calcium is removed from the reaction mixture under vacuum.

 

Thursday, November 14, 2013

Erbium (68)



It has recently been brought to my attention (read, TODAY) that i left out an element of the Lanthanide series. Ladies and gentlemen, I give you:

ERBIUM

Pure erbium metal is soft and malleable and has a bright, silvery, metallic luster. As with other rare-earth metals, its properties depend to a certain extent on impurities present. The metal is fairly stable in air and does not oxidize as rapidly as some of the other rare-earth metals.

Erbium
Symbol: Er
Atomic number: 68
Atomic weight: 167.259 (3) [see note g]
Standard state: solid at 298 K
CAS Registry ID: 7440-52-0
Group name: Lanthanoid
Period in periodic table: 6 (lanthanoid)
Block in periodic table: f-block
Color: silvery white
Classification: Metallic

Historical information
Erbium was discovered by Carl G. Mosander at 1842 in Sweden. Origin of name: named after the village of "Ytterby" near Vaxholm in Sweden. 

(this section gets a bit confusing...)

In 1842 Gustav Mosander separated "yttria", found in the mineral gadolinite, into three fractions which he called yttria, erbia, and terbia. The names erbia and terbia became confused in this early period. After 1860, Mosander's terbia was known as erbia, and after 1877, the earlier known erbia became terbia. The erbia of this period was later shown to consist of five oxides, now known as erbia, scandia, holmia, thulia and ytterbia. Klemm and Bommer first produced reasonably pure erbium metal in 1934 by reducing the anhydrous chloride with potassium vapour.

Physical properties
Melting point: 1802 [or 1529 °C (2784 °F)] K
Boiling point: 3141 [or 2868 °C (5194 °F)] K
Density of solid: 9066 kg m-3

Orbital properties
Ground state electron configuration:  [Xe].4f12.6s2
Shell structure:  2.8.18.30.8.2

Isolation
Erbium metal is available commercially so it is not normally necessary to make it in the laboratory, which is just as well as it is difficult to isolate as the pure metal. This is largely because of the way it is found in nature. The lanthanoids are found in nature in a number of minerals. The most important are xenotime, monazite, and bastnaesite. The first two are orthophosphate minerals LnPO4 (Ln deonotes a mixture of all the lanthanoids except promethium which is vanishingly rare) and the third is a fluoride carbonate LnCO3F. Lanthanoids with even atomic numbers are more common. The most comon lanthanoids in these minerals are, in order, cerium, lanthanum, neodymium, and praseodymium. Monazite also contains thorium and ytrrium which makes handling difficult since thorium and its decomposition products are radioactive.

For many purposes it is not particularly necessary to separate the metals, but if separation into individual metals is required, the process is complex. Initially, the metals are extracted as salts from the ores by extraction with sulphuric acid (H2SO4), hydrochloric acid (HCl), and sodium hydroxide (NaOH). Modern purification techniques for these lanthanoid salt mixtures are ingenious and involve selective complexation techniques, solvent extractions, and ion exchange chromatography.

Pure erbium is available through the reduction of ErF3 with calcium metal.

2ErF3 + 3Ca → 2Er + 3CaF2

This would work for the other calcium halides as well but the product CaF2 is easier to handle under the reaction conditions (heat to 50°C above the melting point of the element in an argon atmosphere). Excess calcium is removed from the reaction mixture under vacuum.