Product Code Database
Example Keywords: silk -wheels $24-149
barcode-scavenger
   » » Wiki: Tantalum
Tag Wiki 'Tantalum'.
Tag

Tantalum is a ; it has symbol Ta and 73. It is named after , a figure in Greek mythology., Orestes Tantalum is a very hard, , lustrous, blue-gray that is highly corrosion-resistant. It is part of the refractory metals group, which are widely used as components of strong . It is a group 5 element, along with and , and it always occurs in geologic sources together with the chemically similar niobium, mainly in the groups , , and .

The chemical inertness and very high melting point of tantalum make it valuable for laboratory and industrial equipment such as and . It is used in tantalum capacitors for electronic equipment such as computers. It is being investigated for use as a material for high-quality superconducting resonators in quantum processors.


History
Tantalum was discovered in Sweden in 1802 by , in two mineral samples – one from Sweden and the other from Finland. One year earlier, had discovered (now niobium). In 1809, the English chemist William Hyde Wollaston compared the oxides of columbium and tantalum, and . Although the two oxides had different measured densities of 5.918 g/cm3 and 7.935 g/cm3, he concluded that they were identical and kept the name tantalum. After Friedrich Wöhler confirmed these results, it was thought that columbium and tantalum were the same element. This conclusion was disputed in 1846 by the German chemist , who argued that there were two additional elements in the tantalite sample, and he named them after the children of : niobium (from ), and pelopium (from ). The supposed element "pelopium" was later identified as a mixture of tantalum and niobium, and it was found that the niobium was identical to the columbium already discovered in 1801 by Hatchett.

The differences between tantalum and niobium were demonstrated unequivocally in 1864 by Christian Wilhelm Blomstrand, and Henri Etienne Sainte-Claire Deville, as well as by Louis J. Troost, who determined the empirical formulas of some of their compounds in 1865. Further confirmation came from the Swiss chemist Jean Charles Galissard de Marignac, in 1866, who proved that there were only two elements. These discoveries did not stop scientists from publishing articles about the so-called until 1871. De Marignac was the first to produce the metallic form of tantalum in 1864, when he tantalum chloride by heating it in an atmosphere of .Marietjie Ungerer. Separation of Tantalum and Niobium by Solvent Extraction. page 22. Early investigators had only been able to produce impure tantalum, and the first relatively pure ductile metal was produced by Werner von Bolton in in 1903. Wires made with metallic tantalum were used for filaments until replaced it in widespread use.

The name tantalum was derived from the name of the mythological Tantalus, the father of Niobe in . In the story, he had been punished after death by being condemned to stand knee-deep in water with perfect fruit growing above his head, both of which eternally tantalized him. (If he bent to drink the water, it drained below the level he could reach, and if he reached for the fruit, the branches moved out of his grasp.) Anders Ekeberg wrote "This metal I call tantalum ... partly in allusion to its incapacity, when immersed in acid, to absorb any and be saturated."

For decades, the commercial technology for separating tantalum from niobium involved the fractional crystallization of potassium heptafluorotantalate away from potassium oxypentafluoroniobate monohydrate, a process that was discovered by Jean Charles Galissard de Marignac in 1866. This method has been supplanted by solvent extraction from fluoride-containing solutions of tantalum.

(1994). 9780849360718, CRC Press.


Characteristics

Physical properties
Tantalum is dark (blue-gray),
(2007). 9780865165731, Bolchazy-Carducci Publishers.
dense, ductile, very hard, easily fabricated, and highly conductive of heat and electricity. The metal is highly resistant to by : at temperatures below 150 ° tantalum is almost completely immune to attack by the normally aggressive . It can be dissolved with hydrofluoric acid or acidic solutions containing the ion and , as well as with molten potassium hydroxide. Tantalum's high melting point of 3017 °C (boiling point 5458 °C) is exceeded among the elements only by , , and for metals, and .

Tantalum exists in two crystalline phases, alpha and beta. The alpha phase is stable at all temperatures up to the melting point and has body-centered cubic structure with lattice constant a = 0.33029 nm at 20 °C. It is relatively , has Knoop hardness 200–400 HN and electrical resistivity 15–60 μΩ⋅cm. The beta phase is hard and brittle; its crystal symmetry is (space group P42/mnm, a = 1.0194 nm, c = 0.5313 nm), Knoop hardness is 1000–1300 HN and electrical resistivity is relatively high at 170–210 μΩ⋅cm. The beta phase is metastable and converts to the alpha phase upon heating to 750–775 °C. Bulk tantalum is almost entirely alpha phase, and the beta phase usually exists as thin films obtained by magnetron , chemical vapor deposition or from a molten salt solution.


Isotopes
Natural tantalum consists of two stable : 180mTa (0.012%) and 181Ta (99.988%). 180mTa ( m denotes a metastable state) is predicted to decay in three ways: isomeric transition to the of 180Ta, to 180, or electron capture to 180. However, radioactivity of this has never been observed, and only a lower limit on its of 2.9 years has been set. The ground state of 180Ta has a half-life of only 8 hours. Among primordial nuclides (half-life > 108 years) 180mTa is the only and the rarest of all (calculated from the elemental abundance of tantalum and the isotopic abundance of 180mTa within it).

Tantalum has been examined theoretically as a "" material for ( is the better-known hypothetical salting material). An external shell of tantalum would be irradiated by the intense neutron flux from the weapon, transmuting it into the radioactive isotope 182Ta, whose gamma rays would significantly increase the radioactivity of the for months. Such "salted" weapons are not known to have been built, tested, or used.

Tantalum is used as a target material for spallation by high-energy proton beams for the production of a large number of isotopes including 8Li, 80Rb, and 160Yb.


Chemical compounds
Tantalum forms compounds in oxidation states −3 to +5. Most commonly encountered are oxides of Ta(V), which includes all minerals. The chemical properties of Ta and Nb are very similar. In aqueous media, Ta only exhibits the +5 oxidation state. Like niobium, tantalum is barely soluble in dilute solutions of hydrochloric, , and due to the precipitation of hydrous Ta(V) oxide. In basic media, Ta can be solubilized due to the formation of polyoxotantalate species.


Oxides, nitrides, carbides, sulfides
Tantalum pentoxide (Ta2O5) is the most important compound from the perspective of applications. Oxides of tantalum in lower oxidation states are numerous, including many , and are lightly studied or poorly characterized.

Tantalates, compounds containing TaO43− or TaO3 are numerous. Lithium tantalate (LiTaO3) adopts a perovskite structure. tantalate (LaTaO4) contains isolated tetrahedra.

(2025). 9783110177701, de Gruyter.

As in the cases of other , the hardest known compounds of tantalum are nitrides and carbides. , TaC, like the more commonly used , is a hard that is used in cutting tools. Tantalum(III) nitride is used as a thin film insulator in some microelectronic fabrication processes.

The best studied chalcogenide is Tantalum sulfide (TaS2), a layered , as seen for other transition metal dichalcogenides. A tantalum-tellurium alloy forms .


Halides
Tantalum halides span the oxidation states of +5, +4, and +3. Tantalum pentafluoride (TaF5) is a white solid with a melting point of 97.0 °C. The anion TaF72- is used for its separation from niobium. The chloride , which exists as a dimer, is the main reagent in synthesis of new Ta compounds. It hydrolyzes readily to an . The lower halides and , feature Ta-Ta bonds.
(2025). 9780444516046, Elsevier. .


Organotantalum compounds
Organotantalum compounds include pentamethyltantalum, mixed alkyltantalum chlorides, alkyltantalum hydrides, alkylidene complexes, as well as cyclopentadienyl derivatives of the same. Diverse salts and substituted derivatives are known for the hexacarbonyl Ta(CO)6 and related .


Occurrence
Tantalum is estimated to make up about 1 ppm
(2025). 9780198503408, Oxford University Press.
or 2 ppm of the Earth's crust by weight. There are many species of tantalum minerals, only some of which are so far being used by industry as raw materials: (a series consisting of tantalite-(Fe), tantalite-(Mn), and tantalite-(Mg)), (now a group name), , (actually euxenite-(Y)), and (actually polycrase-(Y)). Tantalite (, )Ta26 is the most important mineral for tantalum extraction. Tantalite has the same mineral structure as (, ) (Ta, )26; when there is more tantalum than niobium it is called tantalite and when there is more niobium than tantalum is it called columbite (or ). The high density of tantalite and other tantalum containing minerals makes the use of gravitational separation the best method. Other minerals include and .

was the main producer of tantalum prior to the 2010s, with Global Advanced Metals (formerly known as ) being the largest tantalum mining company in that country. They operate two mines in Western Australia, Greenbushes in the southwest and in the region. The Wodgina mine was reopened in January 2011 after mining at the site was suspended in late 2008 due to the 2008 financial crisis. Less than a year after it reopened, Global Advanced Metals announced that due to again "... softening tantalum demand ...", and other factors, tantalum mining operations were to cease at the end of February 2012. Wodgina produces a primary tantalum concentrate which is further upgraded at the Greenbushes operation before being sold to customers. Whereas the large-scale producers of niobium are in and , the ore there also yields a small percentage of tantalum. Some other countries such as , , and mine ores with a higher percentage of tantalum, and they produce a significant percentage of the world's output of it. Tantalum is also produced in and as a by-product of the mining there. During gravitational separation of the ores from placer deposits, not only is (SnO2) found, but a small percentage of tantalite also included. The slag from the tin smelters then contains economically useful amounts of tantalum, which is leached from the slag.

World tantalum mine production has undergone an important geographic shift since the start of the 21st century when production was predominantly from Australia and Brazil. Beginning in 2007 and through 2014, the major sources of tantalum production from mines dramatically shifted to the Democratic Republic of the Congo, , and some other African countries. Future sources of supply of tantalum, in order of estimated size, are being explored in , , , China, Mozambique, Canada, Australia, the , , and Brazil.


Status as a conflict resource
Tantalum is considered a conflict resource. , the industrial name for a mineral from which niobium and tantalum are extracted, Tantalum-Niobium International Study Center: Coltan Retrieved 2008-01-27 can also be found in , which is why tantalum is being linked to warfare in the Democratic Republic of the Congo (formerly ). According to an October 23, 2003 report, the smuggling and exportation of coltan has helped fuel the war in the Congo, a crisis that has resulted in approximately 5.4 million deaths since 1998 – making it the world's deadliest documented conflict since World War II. Ethical questions have been raised about responsible corporate behavior, human rights, and endangering wildlife, due to the exploitation of resources such as coltan in the armed conflict regions of the .
(2025). 9781903703106
The United States Geological Survey reports in its yearbook that this region produced a little less than 1% of the world's tantalum output in 2002–2006, peaking at 10% in 2000 and 2008. USGS data published in January 2021 indicated that close to 40% of the world's tantalum mine production came from the Democratic Republic of the Congo, with another 18% coming from neighboring and .


Production and fabrication
Several steps are involved in the extraction of tantalum from tantalite. First, the mineral is and concentrated by gravity separation. This is generally carried out near the site.


Refining
The refining of tantalum from its ores is one of the more demanding separation processes in industrial metallurgy. The chief problem is that tantalum ores contain significant amounts of , which has chemical properties almost identical to those of Ta. A large number of procedures have been developed to address this challenge.

In modern times, the separation is achieved by . Extraction begins with leaching the ore with hydrofluoric acid together with or hydrochloric acid. This step allows the tantalum and niobium to be separated from the various non-metallic impurities in the rock. Although Ta occurs as various minerals, it is conveniently represented as the pentoxide, since most oxides of tantalum(V) behave similarly under these conditions. A simplified equation for its extraction is thus:

Ta2O5 + 14 HF → 2 H2TaF7 + 5 H2O

Completely analogous reactions occur for the niobium component, but the hexafluoride is typically predominant under the conditions of the extraction.

Nb2O5 + 12 HF → 2 HNbF6 + 5 H2O
These equations are simplified: it is suspected that bisulfate (HSO4) and chloride compete as ligands for the Nb(V) and Ta(V) ions, when sulfuric and hydrochloric acids are used, respectively. The tantalum and niobium fluoride complexes are then removed from the solution by liquid-liquid extraction into , such as , , and methyl isobutyl ketone. This simple procedure allows the removal of most metal-containing impurities (e.g. iron, manganese, titanium, zirconium), which remain in the aqueous phase in the form of their and other complexes.

Separation of the tantalum from niobium is then achieved by lowering the of the acid mixture, which causes the niobium to dissolve in the aqueous phase. It is proposed that H2NbOF5 is formed under these conditions. Subsequent to removal of the niobium, the solution of purified H2TaF7 is neutralised with aqueous to precipitate hydrated tantalum oxide as a solid, which can be to tantalum pentoxide (Ta2O5).

(2025). 9780080529028, Elsevier.

Instead of hydrolysis, the H2TaF7 can be treated with potassium fluoride to produce potassium heptafluorotantalate:

H2TaF7 + 2 KF → K2TaF7 + 2 HF
Unlike H2TaF7, the potassium salt is readily crystallized and handled as a solid.

K2TaF7 can be converted to metallic tantalum by reduction with , at approximately 800 °C in .

K2TaF7 + 5 Na → Ta + 5 NaF + 2 KF

In an older method, called the Marignac process, the mixture of H2TaF7 and H2NbOF5 was converted to a mixture of K2TaF7 and K2NbOF5, which was then separated by fractional crystallization, exploiting their different water solubilities.


Electrolysis
Tantalum can also be refined by electrolysis, using a modified version of the Hall–Héroult process. Instead of requiring the input oxide and output metal to be in liquid form, tantalum electrolysis operates on non-liquid powdered oxides. The initial discovery came in 1997 when Cambridge University researchers immersed small samples of certain oxides in baths of molten salt and reduced the oxide with electric current. The cathode uses powdered metal oxide. The anode is made of carbon. The molten salt at is the electrolyte. The first refinery has enough capacity to supply 3–4% of annual global demand.


Fabrication and metalworking
All of tantalum must be done in an inert atmosphere of or in order to shield it from contamination with atmospheric gases. Tantalum is not . Grinding tantalum is difficult, especially so for annealed tantalum. In the annealed condition, tantalum is extremely and can be readily formed as metal sheets.


Applications

Electronics
The major use for tantalum, as the metal powder, is in the production of electronic components, mainly and some high-power . Tantalum electrolytic capacitors exploit the tendency of tantalum to form a protective surface layer, using tantalum powder, pressed into a pellet shape, as one "plate" of the capacitor, the oxide as the , and an electrolytic solution or conductive solid as the other "plate". Because the dielectric layer can be very thin (thinner than the similar layer in, for instance, an aluminium electrolytic capacitor), a high can be achieved in a small volume. Because of the size and weight advantages, tantalum capacitors are attractive for portable telephones, personal computers, automotive electronics and .


Alloys
Tantalum is also used to produce a variety of that have high melting points, strength, and ductility. Alloyed with other metals, it is also used in making carbide tools for metalworking equipment and in the production of for jet engine components, chemical process equipment, , missile parts, heat exchangers, tanks, and vessels. Because of its ductility, tantalum can be drawn into fine wires or filaments, which are used for evaporating metals such as .

Tantalum is inert against most acids except hydrofluoric acid and hot , and hot solutions also cause tantalum to corrode. This property makes it a useful metal for chemical reaction vessels and pipes for corrosive liquids. Heat exchanging coils for the steam heating of hydrochloric acid are made from tantalum. Tantalum was extensively used in the production of ultra high frequency for radio transmitters. Tantalum is capable of capturing oxygen and nitrogen by forming nitrides and oxides and therefore helped to sustain the high vacuum needed for the tubes when used for internal parts such as grids and plates.


Surgical uses
Tantalum is widely used in surgery because of two unique characteristics of tantalum. Tantalum's hardness and ductility is useful in making sharp, durable surgical instruments and also for monofilament sutures. However, a completely unrelated use for tantalum in surgery arises from its unique ability to form a lasting and durable structural bond with human hard tissue, making it uniquely useful for bone and dental implants. Tantalum coatings are increasingly used in the construction of complex tantalum-coated titanium surgical implants due to the tantalum plating's ability to form a strong and biologically stable bond to hard tissue. An incidental consequence of its use for durable surgical implants is that tantalum implants are considered to be acceptable for patients undergoing MRI procedures because tantalum is a non-ferrous, non-magnetic metal.


Other uses
Tantalum was used by to shield components of spacecraft, such as Voyager 1 and Voyager 2, from radiation.
(2025). 9780525954323, Dutton.
The high melting point and oxidation resistance led to the use of the metal in the production of parts. Tantalum is extremely inert and is therefore formed into a variety of corrosion resistant parts, such as , valve bodies, and tantalum fasteners. Due to its high density, and explosively formed penetrator liners have been constructed from tantalum. Tantalum greatly increases the armor penetration capabilities of a shaped charge due to its high density and high melting point.
(2025). 9780471649526, Wiley-Interscience. .
It is also occasionally used in precious e.g. from , F. P. Journe, , Montblanc, , and . Tantalum oxide is used to make special high for lenses.
(1985). 9780824773090, CRC Press.
Spherical tantalum powder, produced by atomizing molten tantalum using gas or liquid, is commonly used in additive manufacturing due to its uniform shape, excellent , and high melting point.


Environmental issues
Tantalum receives far less attention in the environmental field than it does in other geosciences. Upper Crust Concentration (UCC) and the Nb/Ta ratio in the upper crust and in minerals are available because these measurements are useful as a geochemical tool. The latest value for upper crust concentration is 0.92 ppm, and the Nb/Ta(w/w) ratio stands at 12.7.

Little data is available on tantalum concentrations in the different environmental compartments, especially in natural waters where reliable estimates of 'dissolved' tantalum concentrations in seawater and freshwaters have not even been produced. Some values on dissolved concentrations in oceans have been published, but they are contradictory. Values in freshwaters fare little better, but, in all cases, they are probably below 1 ng L−1, since 'dissolved' concentrations in natural waters are well below most current analytical capabilities. Analysis requires pre-concentration procedures that, for the moment, do not give consistent results. And in any case, tantalum appears to be present in natural waters mostly as particulate matter rather than dissolved.

Values for concentrations in soils, bed sediments and atmospheric aerosols are easier to come by. Values in soils are close to 1 ppm and thus to UCC values. This indicates detrital origin. For atmospheric aerosols the values available are scattered and limited. When tantalum enrichment is observed, it is probably due to loss of more water-soluble elements in aerosols in the clouds.

Pollution linked to human use of the element has not been detected. Tantalum appears to be a very conservative element in biogeochemical terms, but its cycling and reactivity are still not fully understood.


Precautions
Compounds containing tantalum are rarely encountered in the laboratory. The metal is highly and is used for body implants and , therefore attention may be focused on other elements or the physical nature of the chemical compound.

People can be exposed to tantalum in the workplace by breathing it in, skin contact, or eye contact. The Occupational Safety and Health Administration (OSHA) has set the legal limit (permissible exposure limit) for tantalum exposure in the workplace as 5 mg/m3 over an 8-hour workday. The National Institute for Occupational Safety and Health (NIOSH) has set a recommended exposure limit (REL) of 5 mg/m3 over an 8-hour workday and a short-term limit of 10 mg/m3. There is a paradox arising because of tantalum's ability to form a strong and permanent bond with bone tissue: at levels of 2500 mg/m3, tantalum dust becomes if tantalum dust accidentally bonds with the wrong tissue.


External links

Page 1 of 1
1
Page 1 of 1
1

Account

Social:
Pages:  ..   .. 
Items:  .. 

Navigation

General: Atom Feed Atom Feed  .. 
Help:  ..   .. 
Category:  ..   .. 
Media:  ..   .. 
Posts:  ..   ..   .. 

Statistics

Page:  .. 
Summary:  .. 
1 Tags
10/10 Page Rank
5 Page Refs
2s Time