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151-518: The Chrysler Pentastar engine family is a series of aluminium ( die-cast cylinder block ) dual overhead cam 24-valve gasoline V6 engines introduced for the 2011 model year in Chrysler , Dodge , and Jeep vehicles. The engine was initially named " Phoenix ," but the name was changed before the official launch due to a trademark conflict; the Pentastar name is derived from the trademark of

302-491: A precipitate of aluminium hydroxide , Al(OH) 3 , forms. This is useful for clarification of water, as the precipitate nucleates on suspended particles in the water, hence removing them. Increasing the pH even further leads to the hydroxide dissolving again as aluminate , [Al(H 2 O) 2 (OH) 4 ] , is formed. Aluminium hydroxide forms both salts and aluminates and dissolves in acid and alkali, as well as on fusion with acidic and basic oxides. This behavior of Al(OH) 3

453-525: A "less classical sound". This name persisted: although the -um spelling was occasionally used in Britain, the American scientific language used -ium from the start. Most scientists throughout the world used -ium in the 19th century; and it was entrenched in several other European languages, such as French , German , and Dutch . In 1828, an American lexicographer, Noah Webster , entered only

604-499: A Swedish chemist, Jöns Jacob Berzelius , in which the name aluminium is given to the element that would be synthesized from alum. (Another article in the same journal issue also refers to the metal whose oxide is the basis of sapphire , i.e. the same metal, as to aluminium .) A January 1811 summary of one of Davy's lectures at the Royal Society mentioned the name aluminium as a possibility. The next year, Davy published

755-479: A brown mass of potassium bismuthate. The solution chemistry of bismuth is characterised by the formation of oxyanions; it forms anionic bismuthates in strongly basic solutions. Bismuth forms Zintl phases such as NaBi, Rb 7 In 4 Bi 6 and Ba 11 Cd 8 Bi 14 . Bailar et al. refer to bismuth as being, 'the least "metallic" metal in its physical properties' given its brittle nature (and possibly) 'the lowest electrical conductivity of all metals.' Moscovium

906-561: A chemistry textbook in which he used the spelling aluminum . Both spellings have coexisted since. Their usage is currently regional: aluminum dominates in the United States and Canada; aluminium is prevalent in the rest of the English-speaking world. In 1812, British scientist Thomas Young wrote an anonymous review of Davy's book, in which he proposed the name aluminium instead of aluminum , which he thought had

1057-418: A close-packed body-centered cubic structure. It should be a very dense metal, with its density of 22–24 g/cm being around that of osmium and iridium , the densest stable elements. Roentgenium chemistry is expected to be dominated by the +3 valence state, similarly to gold, in which it should similarly behave as a transition metal. Roentgenium oxide (Rg 2 O 3 ) should be amphoteric; stable compounds in

1208-410: A common +1 oxidation state and a less common +3 oxidation state, although their relative stabilities may change depending on the complexing ligands or the degree of hydrolysis. Moscovium(I) oxide (Mc 2 O) should be quite basic, like that of thallium, while moscovium(III) oxide (Mc 2 O 3 ) should be amphoteric, like that of bismuth. Selenium is a soft (MH 2.0) and brittle semi-metallic element. It

1359-416: A few hundred degrees, cadmium represents a toxicity hazard due to the release of cadmium vapour; when heated to its boiling point in air (just above 1000 K; 725 C; 1340 F; cf steel ~2700 K; 2425 C; 4400 F), the cadmium vapour oxidizes, 'with a reddish-yellow flame, dispersing as an aerosol of potentially lethal CdO particles.' Cadmium is otherwise stable in air and in water, at ambient conditions, protected by

1510-482: A good strength-to-weight ratio and excellent ductility; its mechanical strength can be improved considerably with the use of alloying additives; its very high thermal conductivity can be put to good use in heat sinks and heat exchangers ; and it has a high electrical conductivity. At lower temperatures, aluminium increases its deformation strength (as do most materials) whilst maintaining ductility (as do face-centred cubic metals generally). Chemically, bulk aluminium

1661-471: A hexagonal close-packed crystalline structure, albeit based on extrapolation from those of the lighter group 13 elements: its density is expected to be around 16 g/cm . A standard electrode potential of +0.6 V is predicted for the Nh /Nh couple. The relativistic stabilisation of the 7s electrons is very high and hence nihonium should predominantly form the +1 oxidation state; nevertheless, as for copernicium,

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1812-548: A layer of cadmium oxide. Mercury is a liquid at room temperature. It has the weakest metallic bonding of all, as indicated by its bonding energy (61 kJ/mol) and melting point (−39 °C) which, together, are the lowest of all the metallic elements. Solid mercury (MH 1.5) has a distorted crystalline structure, with mixed metallic-covalent bonding, and a BCN of 6. "All of the [Group 12] metals, but especially mercury, tend to form covalent rather than ionic compounds." The oxide of mercury in its preferred oxidation state (HgO; +2)

1963-545: A low melting point and a high thermal conductivity. Its strength is halved at 200 °C, and for many of its alloys is minimal at 300 °C. The latter three properties of aluminium limit its use to situations where fire protection is not required, or necessitate the provision of increased fire protection. It bonds covalently in most of its compounds; has an amphoteric oxide; and can form anionic aluminates. Aluminium forms Zintl phases such as LiAl, Ca 3 Al 2 Sb 6 , and SrAl 2 . A thin protective layer of oxide confers

2114-507: A metal or a non-metal. It exhibits poor electrical conductivity which, like a metal, decreases with temperature. It has a relatively open and partially covalent crystalline structure (BCN 3+3). Antimony forms covalent bonds with most other elements. The oxide in its preferred oxidation state (Sb 2 O 3 , +3) is amphoteric. Antimony forms a series of anionic antimonites and antimonates such as NaSbO 2 and AlSbO 4 , and Zintl phases such as K 5 Sb 4 , Sr 2 Sb 3 and BaSb 3 . Bismuth

2265-545: A nonmetal, less commonly as a metalloid and occasionally as a metal. Unlike its lighter congener iodine, evidence for diatomic astatine is sparse and inconclusive. In 2013, on the basis of relativistic modelling, astatine was predicted to be a monatomic metal, with a face-centered cubic crystalline structure. As such, astatine could be expected to have a metallic appearance; show metallic conductivity; and have excellent ductility, even at cryogenic temperatures. It could also be expected to show significant nonmetallic character, as

2416-406: A post-transition metal similar to mercury, although the relativistic stabilisation of the 7s orbitals means that this oxidation state involves giving up 6d rather than 7s electrons. A concurrent relativistic destabilisation of the 6d orbitals should allow higher oxidation states such as +3 and +4 with electronegative ligands, such as the halogens. A very high standard reduction potential of +2.1 V

2567-441: A probable cause for it being soft with a low melting point and low electrical resistivity . Aluminium metal has an appearance ranging from silvery white to dull gray depending on its surface roughness . Aluminium mirrors are the most reflective of all metal mirrors for near ultraviolet and far infrared light. It is also one of the most reflective for light in the visible spectrum, nearly on par with silver in this respect, and

2718-683: A process termed passivation . Because of its general resistance to corrosion, aluminium is one of the few metals that retains silvery reflectance in finely powdered form, making it an important component of silver-colored paints. Aluminium is not attacked by oxidizing acids because of its passivation. This allows aluminium to be used to store reagents such as nitric acid , concentrated sulfuric acid , and some organic acids. In hot concentrated hydrochloric acid , aluminium reacts with water with evolution of hydrogen, and in aqueous sodium hydroxide or potassium hydroxide at room temperature to form aluminates —protective passivation under these conditions

2869-430: A reasonable degree of corrosion resistance. It is susceptible to attack in low pH (<4) and high (> 8.5) pH conditions, a phenomenon that is generally more pronounced in the case of commercial purity aluminium and aluminium alloys. Given many of these properties and its proximity to the dividing line between metals and nonmetals , aluminium is occasionally classified as a metalloid. Despite its shortcomings, it has

3020-525: A refractory material, and in ceramics , as well as being the starting material for the electrolytic production of aluminium. Sapphire and ruby are impure corundum contaminated with trace amounts of other metals. The two main oxide-hydroxides, AlO(OH), are boehmite and diaspore . There are three main trihydroxides: bayerite , gibbsite , and nordstrandite , which differ in their crystalline structure ( polymorphs ). Many other intermediate and related structures are also known. Most are produced from ores by

3171-474: A stable noble gas configuration. Accordingly, the combined first three ionization energies of aluminium are far lower than the fourth ionization energy alone. Such an electron configuration is shared with the other well-characterized members of its group, boron , gallium , indium , and thallium ; it is also expected for nihonium . Aluminium can surrender its three outermost electrons in many chemical reactions (see below ). The electronegativity of aluminium

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3322-455: A thin protective oxide layer. Pure tin has no structural uses. It is used in lead-free solders , and as a hardening agent in alloys of other metals, such as copper, lead, titanium and zinc. Lead is a soft metal (MH 1.5, but hardens close to melting) which, in many cases, is unable to support its own weight. It has a close-packed structure (BCN 12) but an abnormally large inter-atomic distance that has been attributed to partial ionisation of

3473-537: A transition metal in its preferred oxidation state of +2. Stable compounds in which copper is in its less preferred oxidation state of +1 (Cu 2 O, CuCl, CuBr, CuI and CuCN, for example) have significant covalent character. The oxide (CuO) is amphoteric, with predominating basic properties; it can be fused with alkali oxides (M 2 O; M = Na, K) to give anionic oxycuprates (M 2 CuO 2 ). Copper forms Zintl phases such as Li 7 CuSi 2 and M 3 Cu 3 Sb 4 (M = Y, La, Ce, Pr, Nd, Sm, Gd, Tb, Dy, Ho, or Er). Silver

3624-512: A transition metal. Zinc is a soft metal (MH 2.5) with poor mechanical properties. It has a crystalline structure (BCN 6+6) that is slightly distorted from the ideal. Many zinc compounds are markedly covalent in character. The oxide and hydroxide of zinc in its preferred oxidation state of +2, namely ZnO and Zn(OH) 2 , are amphoteric; it forms anionic zincates in strongly basic solutions. Zinc forms Zintl phases such as LiZn, NaZn 13 and BaZn 13 . Highly purified zinc, at room temperature,

3775-820: A variety of wet processes using acid and base. Heating the hydroxides leads to formation of corundum. These materials are of central importance to the production of aluminium and are themselves extremely useful. Some mixed oxide phases are also very useful, such as spinel (MgAl 2 O 4 ), Na-β-alumina (NaAl 11 O 17 ), and tricalcium aluminate (Ca 3 Al 2 O 6 , an important mineral phase in Portland cement ). The only stable chalcogenides under normal conditions are aluminium sulfide (Al 2 S 3 ), selenide (Al 2 Se 3 ), and telluride (Al 2 Te 3 ). All three are prepared by direct reaction of their elements at about 1,000 °C (1,800 °F) and quickly hydrolyze completely in water to yield aluminium hydroxide and

3926-575: A way of purifying bauxite to yield alumina, now known as the Bayer process , in 1889. Modern production of aluminium is based on the Bayer and Hall–Héroult processes. As large-scale production caused aluminium prices to drop, the metal became widely used in jewelry, eyeglass frames, optical instruments, tableware, and foil , and other everyday items in the 1890s and early 20th century. Aluminium's ability to form hard yet light alloys with other metals provided

4077-454: A well shielded [Ne] noble gas core rather than the less well shielded [Ar]3d , [Kr]4d or [Xe]4f 5d core of the post-transition metals. The small radius of the aluminium ion combined with its high charge make it a strongly polarizing species, prone to covalency. Aluminium in pure form is a soft metal (MH 3.0) with low mechanical strength. It has a close-packed structure (BCN 12) showing some evidence of partially directional bonding. It has

4228-734: Is Al : while it was present along with stable Al in the interstellar medium from which the Solar System formed, having been produced by stellar nucleosynthesis as well, its half-life is only 717,000 years and therefore a detectable amount has not survived since the formation of the planet. However, minute traces of Al are produced from argon in the atmosphere by spallation caused by cosmic ray protons. The ratio of Al to Be has been used for radiodating of geological processes over 10 to 10  year time scales, in particular transport, deposition, sediment storage, burial times, and erosion. Most meteorite scientists believe that

4379-434: Is Al. Al was present in the early Solar System with abundance of 0.005% relative to Al but its half-life of 728,000 years is too short for any original nuclei to survive; Al is therefore extinct . Unlike for Al, hydrogen burning is the primary source of Al, with the nuclide emerging after a nucleus of Mg catches a free proton. However, the trace quantities of Al that do exist are the most common gamma ray emitter in

4530-407: Is paramagnetic and thus essentially unaffected by static magnetic fields. The high electrical conductivity, however, means that it is strongly affected by alternating magnetic fields through the induction of eddy currents . Aluminium combines characteristics of pre- and post-transition metals. Since it has few available electrons for metallic bonding, like its heavier group 13 congeners, it has

4681-483: Is 1.61 (Pauling scale). A free aluminium atom has a radius of 143  pm . With the three outermost electrons removed, the radius shrinks to 39 pm for a 4-coordinated atom or 53.5 pm for a 6-coordinated atom. At standard temperature and pressure , aluminium atoms (when not affected by atoms of other elements) form a face-centered cubic crystal system bound by metallic bonding provided by atoms' outermost electrons; hence aluminium (at these conditions)

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4832-418: Is a post-transition metal in the boron group ; as is common for the group, aluminium forms compounds primarily in the +3 oxidation state . The aluminium cation Al is small and highly charged ; as such, it has more polarizing power , and bonds formed by aluminium have a more covalent character. The strong affinity of aluminium for oxygen leads to the common occurrence of its oxides in nature. Aluminium

4983-548: Is a metal. This crystal system is shared by many other metals, such as lead and copper ; the size of a unit cell of aluminium is comparable to that of those other metals. The system, however, is not shared by the other members of its group: boron has ionization energies too high to allow metallization, thallium has a hexagonal close-packed structure, and gallium and indium have unusual structures that are not close-packed like those of aluminium and thallium. The few electrons that are available for metallic bonding in aluminium are

5134-452: Is a moderately hard (MH 3.5) and brittle semi-metallic element. It is commonly regarded as a metalloid, or by some other authors as either a metal or a non-metal. It exhibits poor electrical conductivity which, like a metal, decreases with temperature. It has a relatively open and partially covalent crystalline structure (BCN 3+3). Arsenic forms covalent bonds with most other elements. The oxide in its preferred oxidation state (As 2 O 3 , +3)

5285-541: Is a radioactive, soft metal with a hardness similar to lead. It has a simple cubic crystalline structure characterised (as determined by electron density calculations) by partially directional bonding, and a BCN of 6. Such a structure ordinarily results in very low ductility and fracture resistance however polonium has been predicted to be a ductile metal. It forms a covalent hydride; its halides are covalent, volatile compounds, resembling those of tellurium. The oxide of polonium in its preferred oxidation state (PoO 2 ; +4)

5436-565: Is a semiconductor with a band gap of 0.32 to 0.38 eV. Tellurium forms covalent bonds with most other elements, noting it has an extensive organometallic chemistry and that many tellurides can be regarded as metallic alloys. The common oxide of tellurium ( TeO 2 ) is amphoteric. Tellurium forms a series of anionic tellurites and tellurates such as Na 2 TeO 3 , Na 6 TeO 6 , and Rb 6 Te 2 O 9 (the last containing tetrahedral TeO 4 and trigonal bipyramidal TeO 5 anions), as well as Zintl phases such as NaTe 3 . Polonium

5587-508: Is a soft metal (MH 2.5) that is too brittle for any structural use. It has an open-packed crystalline structure (BCN 3+3) with bonding that is intermediate between metallic and covalent. For a metal, it has exceptionally low electrical and thermal conductivity. Most of the ordinary compounds of bismuth are covalent in nature. The oxide, Bi 2 O 3 is predominantly basic but will act as a weak acid in warm, very concentrated KOH. It can also be fused with potassium hydroxide in air, resulting in

5738-402: Is a soft metal (MH 2.5–3) with low mechanical strength. It has a close-packed face-centred cubic structure (BCN 12). The chemistry of silver is dominated by its +1 valence state in which it shows generally similar physical and chemical properties to compounds of thallium, a main group metal, in the same oxidation state. It tends to bond covalently in most of its compounds. The oxide (Ag 2 O)

5889-700: Is a soft, exceptionally weak metal (MH 1.5); a 1-cm thick rod will bend easily under mild finger pressure. It has an irregularly coordinated crystalline structure (BCN 4+2) associated with incompletely ionised atoms. All of the Group 14 elements form compounds in which they are in the +4, predominantly covalent, oxidation state; even in the +2 oxidation state tin generally forms covalent bonds. The oxides of tin in its preferred oxidation state of +2, namely SnO and Sn(OH) 2 , are amphoteric; it forms stannites in strongly basic solutions. Below 13 °C (55.4 °F) tin changes its structure and becomes 'grey tin', which has

6040-483: Is a soft, reactive metal (MH 1.0), so much so that it has no structural uses. It has a close-packed crystalline structure (BCN 6+6) but an abnormally large interatomic distance that has been attributed to partial ionisation of the thallium atoms. Although compounds in the +1 (mostly ionic) oxidation state are the more numerous, thallium has an appreciable chemistry in the +3 (largely covalent) oxidation state, as seen in its chalcogenides and trihalides. It and aluminium are

6191-503: Is a strongly electropositive metal, with a high negative electrode potential . Gallium is a soft, brittle metal (MH 1.5) that melts at only a few degrees above room temperature. It has an unusual crystalline structure featuring mixed metallic-covalent bonding and low symmetry (BCN 7 i.e. 1+2+2+2). It bonds covalently in most of its compounds, has an amphoteric oxide; and can form anionic gallates. Gallium forms Zintl phases such as Li 2 Ga 7 , K 3 Ga 13 and YbGa 2 . It

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6342-522: Is almost never found in the elemental state; instead it is found in oxides or silicates. Feldspars , the most common group of minerals in the Earth's crust, are aluminosilicates. Aluminium also occurs in the minerals beryl , cryolite , garnet , spinel , and turquoise . Impurities in Al 2 O 3 , such as chromium and iron , yield the gemstones ruby and sapphire , respectively. Native aluminium metal

6493-405: Is also easily machined and cast . Aluminium is an excellent thermal and electrical conductor , having around 60% the conductivity of copper , both thermal and electrical, while having only 30% of copper's density. Aluminium is capable of superconductivity , with a superconducting critical temperature of 1.2 kelvin and a critical magnetic field of about 100 gauss (10 milliteslas ). It

6644-410: Is amphoteric, as is the corresponding oxoacid in aqueous solution (H 3 AsO 3 ) and congener sulfide (As 2 S 3 ). Arsenic forms a series of anionic arsenates such as Na 3 AsO 3 and PbHAsO 4 , and Zintl phases such as Na 3 As, Ca 2 As and SrAs 3 . Antimony is a soft (MH 3.0) and brittle semi-metallic element. It is commonly regarded as a metalloid, or by some other authors as either

6795-455: Is amphoteric, with acidic properties predominating; it can be fused with alkali hydroxides (MOH; M = Na, K) or calcium oxide (CaO) to give anionic platinates, such as red Na 2 PtO 3 and green K 2 PtO 3 . The hydrated oxide can be dissolved in hydrochloric acid to give the hexachlormetallate(IV), H 2 PtCl 6 . Like gold, which can form compounds containing the −1 auride ion, platinum can form compounds containing platinide ions, such as

6946-407: Is amphoteric, with acidic properties predominating; it forms anionic hydroxoaurates M[Au(OH) 4 ] , where M = Na, K, ½Ba, Tl; and aurates such as NaAuO 2 . Gold is a constituent of Zintl phases such as M 2 AuBi (M = Li or Na); Li 2 AuM (M = In, Tl, Ge, Pb, Sn) and Ca 5 Au 4 . Roentgenium is expected to be similar to its lighter homologue gold in many ways. It is expected to have

7097-540: Is amphoteric, with basic properties predominating. Silver forms a series of oxoargentates (M 3 AgO 2 , M = Na, K, Rb). It is a constituent of Zintl phases such as Li 2 AgM (M = Al, Ga, In, Tl, Si, Ge, Sn or Pb) and Yb 3 Ag 2 . Gold is a soft metal (MH 2.5–3) that is easily deformed. It has a close-packed face-centred cubic structure (BCN 12). The chemistry of gold is dominated by its +3 valence state; all such compounds of gold feature covalent bonding, as do its stable +1 compounds. Gold oxide (Au 2 O 3 )

7248-428: Is amphoteric; it forms anionic plumbates in strongly basic solutions. Lead forms Zintl phases such as CsPb , Sr 31 Pb 20 , La 5 Pb 3 N and Yb 3 Pb 20 . It has reasonable to good corrosion resistance; in moist air it forms a mixed gray coating of oxide, carbonate and sulfate that hinders further oxidation. Flerovium is expected to be a liquid metal due to spin-orbit coupling "tearing" apart

7399-484: Is commonly regarded as a nonmetal, but is sometimes considered a metalloid or even a heavy metal . Selenium has a hexagonal polyatomic (CN 2) crystalline structure. It is a semiconductor with a band gap of 1.7 eV, and a photoconductor meaning its electrical conductivity increases a million-fold when illuminated. Selenium forms covalent bonds with most other elements, noting it can form ionic selenides with highly electropositive metals. The common oxide of selenium ( SeO 3 )

7550-676: Is ductile. It reacts with moist air to form a thin layer of carbonate that prevents further corrosion. Cadmium is a soft, ductile metal (MH 2.0) that undergoes substantial deformation , under load, at room temperature. Like zinc, it has a crystalline structure (BCN 6+6) that is slightly distorted from the ideal. The halides of cadmium, with the exception of the fluoride, exhibit a substantially covalent nature. The oxides of cadmium in its preferred oxidation state of +2, namely CdO and Cd(OH) 2 , are weakly amphoteric; it forms cadmates in strongly basic solutions. Cadmium forms Zintl phases such as LiCd, RbCd 13 and CsCd 13 . When heated in air to

7701-426: Is even less than that of mercury and is likely only higher than that of flerovium. Solid copernicium is expected to crystallise in a close-packed body-centred cubic structure and have a density of about 14.7 g/cm , decreasing to 14.0 g/cm on melting, which is similar to that of mercury (13.534 g/cm ). Copernicium chemistry is expected to be dominated by the +2 oxidation state, in which it would behave like

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7852-472: Is expected for the Cn /Cn couple. In fact, bulk copernicium may even be an insulator with a band gap of 6.4±0.2 V, which would make it similar to the noble gases such as radon , though copernicium has previously been predicted to be a semiconductor or a noble metal instead. Copernicium oxide (CnO) is expected to be predominantly basic. Aluminium sometimes is or is not counted as a post-transition metal. It has

8003-455: Is expected to be a quite reactive metal. A standard reduction potential of −1.5 V for the Mc /Mc couple is expected. This increased reactivity is consistent with the quasi-closed shell of flerovium and the beginning of a new series of elements with the filling of the loosely bound 7p 3/2 subshell, and is rather different from the relative nobility of bismuth. Like thallium, moscovium should have

8154-421: Is expected to be amphoteric, similar to gold oxide and astatine(III) oxide. Oganesson is expected to be a very poor "noble gas" and may even be metallised by its large atomic radius and the weak binding of the easily removed 7p 3/2 electrons: certainly it is expected to be a quite reactive element that is solid at room temperature and has some similarities to tin , as one effect of the spin–orbit splitting of

8305-632: Is expected to be amphoteric. Germanium is a hard (MH 6), very brittle semi-metallic element. It was originally thought to be a poorly conducting metal but has the electronic band structure of a semiconductor . Germanium is usually considered to be a metalloid rather than a metal. Like carbon (as diamond) and silicon, it has a covalent tetrahedral crystalline structure (BCN 4). Compounds in its preferred oxidation state of +4 are covalent. Germanium forms an amphoteric oxide, GeO 2 and anionic germanates, such as Mg 2 GeO 4 . It forms Zintl phases such as LiGe, K 8 Ge 44 and La 4 Ge 3 . Tin

8456-499: Is expected to be less reactive than moscovium. The standard reduction potential of the Lv /Lv couple is expected to be around +0.1 V. It should be most stable in the +2 oxidation state; the 7p 3/2 electrons are expected to be so weakly bound that the first two ionisation potentials of livermorium should lie between those of the reactive alkaline earth metals magnesium and calcium . The +4 oxidation state should only be reachable with

8607-553: Is extremely rare and can only be found as a minor phase in low oxygen fugacity environments, such as the interiors of certain volcanoes. Native aluminium has been reported in cold seeps in the northeastern continental slope of the South China Sea . It is possible that these deposits resulted from bacterial reduction of tetrahydroxoaluminate Al(OH) 4 . Although aluminium is a common and widespread element, not all aluminium minerals are economically viable sources of

8758-438: Is found on Earth primarily in rocks in the crust , where it is the third-most abundant element , after oxygen and silicon , rather than in the mantle , and virtually never as the free metal . It is obtained industrially by mining bauxite , a sedimentary rock rich in aluminium minerals. The discovery of aluminium was announced in 1825 by Danish physicist Hans Christian Ørsted . The first industrial production of aluminium

8909-536: Is greatly reduced by aqueous salts, particularly in the presence of dissimilar metals. Aluminium reacts with most nonmetals upon heating, forming compounds such as aluminium nitride (AlN), aluminium sulfide (Al 2 S 3 ), and the aluminium halides (AlX 3 ). It also forms a wide range of intermetallic compounds involving metals from every group on the periodic table. The vast majority of compounds, including all aluminium-containing minerals and all commercially significant aluminium compounds, feature aluminium in

9060-492: Is in fact more basic than that of gallium. Aluminium also bears minor similarities to the metalloid boron in the same group: AlX 3 compounds are valence isoelectronic to BX 3 compounds (they have the same valence electronic structure), and both behave as Lewis acids and readily form adducts . Additionally, one of the main motifs of boron chemistry is regular icosahedral structures, and aluminium forms an important part of many icosahedral quasicrystal alloys, including

9211-523: Is more ductile than gold, silver or copper, thus being the most ductile of pure metals, but it is less malleable than gold. Like gold, platinum is a chalcophile element in terms of its occurrence in the Earth's crust, preferring to form covalent bonds with sulfur. It behaves like a transition metal in its preferred oxidation states of +2 and +4. There is very little evidence of the existence of simple metal ions in aqueous media; most platinum compounds are (covalent) coordination complexes. The oxide (PtO 2 )

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9362-431: Is more evident in period 4–6 post-transition metals, due to inefficient screening of their nuclear charges by their d and (in the case of the period 6 metals) f electron configurations; the screening power of electrons decreases in the sequence s > p > d > f. The reductions in atomic size due to the interjection of the d- and f-blocks are referred to as, respectively, the 'scandide' or ' d-block contraction ', and

9513-500: Is negligible. Aqua regia also dissolves aluminium. Aluminium is corroded by dissolved chlorides , such as common sodium chloride , which is why household plumbing is never made from aluminium. The oxide layer on aluminium is also destroyed by contact with mercury due to amalgamation or with salts of some electropositive metals. As such, the strongest aluminium alloys are less corrosion-resistant due to galvanic reactions with alloyed copper , and aluminium's corrosion resistance

9664-608: Is normally the case for metals in, or in the vicinity of, the p-block. Astatine oxyanions AtO , AtO 3 and AtO 4 are known, oxyanion formation being a tendency of nonmetals. The hydroxide of astatine At(OH) is presumed to be amphoteric. Astatine forms covalent compounds with nonmetals, including hydrogen astatide HAt and carbon tetraastatide CAt 4 . At anions have been reported to form astatides with silver, thallium, palladium and lead. Pruszyński et al. note that astatide ions should form strong complexes with soft metal cations such as Hg , Pd , Ag and Tl ; they list

9815-521: Is not as important. It is a polymer with the formula (AlH 3 ) n , in contrast to the corresponding boron hydride that is a dimer with the formula (BH 3 ) 2 . Aluminium's per-particle abundance in the Solar System is 3.15 ppm (parts per million). It is the twelfth most abundant of all elements and third most abundant among the elements that have odd atomic numbers, after hydrogen and nitrogen. The only stable isotope of aluminium, Al,

9966-409: Is predominantly basic, but amphoteric if dissolved in concentrated aqueous alkali, or fused with potassium hydroxide in air. The yellow polonate(IV) ion PoO 3 is known in aqueous solutions of low Cl concentration and high pH. Polonides such as Na 2 Po, BePo, ZnPo, CdPo and HgPo feature Po anions; except for HgPo these are some of the more stable of the polonium compounds. Livermorium

10117-416: Is quite soft and lacking in strength. In most applications various aluminium alloys are used instead because of their higher strength and hardness. The yield strength of pure aluminium is 7–11 MPa , while aluminium alloys have yield strengths ranging from 200 MPa to 600 MPa. Aluminium is ductile , with a percent elongation of 50-70%, and malleable allowing it to be easily drawn and extruded . It

10268-751: Is slowly oxidized in moist air at ambient conditions; a protective film of oxide prevents further corrosion. Indium is a soft, highly ductile metal (MH 1.0) with a low tensile strength. It has a partially distorted crystalline structure (BCN 4+8) associated with incompletely ionised atoms. The tendency of indium '...to form covalent compounds is one of the more important properties influencing its electrochemical behavior'. The oxides of indium in its preferred oxidation state of +3, namely In 2 O 3 and In(OH) 3 are weakly amphoteric; it forms anionic indates in strongly basic solutions. Indium forms Zintl phases such as LiIn, Na 2 In and Rb 2 In 3 . Indium does not oxidize in air at ambient conditions. Thallium

10419-429: Is strongly acidic. Selenium forms a series of anionic selenites and selenates such as Na 2 SeO 3 , Na 2 Se 2 O 5 , and Na 2 SeO 4 , as well as Zintl phases such as Cs 4 Se 16 . Tellurium is a soft (MH 2.25) and brittle semi-metallic element. It is commonly regarded as a metalloid, or by some authors either as a metal or a non-metal. Tellurium has a polyatomic (CN 2) hexagonal crystalline structure. It

10570-422: Is surrounded by six fluorine atoms in a distorted octahedral arrangement, with each fluorine atom being shared between the corners of two octahedra. Such {AlF 6 } units also exist in complex fluorides such as cryolite , Na 3 AlF 6 . AlF 3 melts at 1,290 °C (2,354 °F) and is made by reaction of aluminium oxide with hydrogen fluoride gas at 700 °C (1,300 °F). With heavier halides,

10721-547: Is termed amphoterism and is characteristic of weakly basic cations that form insoluble hydroxides and whose hydrated species can also donate their protons. One effect of this is that aluminium salts with weak acids are hydrolyzed in water to the aquated hydroxide and the corresponding nonmetal hydride: for example, aluminium sulfide yields hydrogen sulfide . However, some salts like aluminium carbonate exist in aqueous solution but are unstable as such; and only incomplete hydrolysis takes place for salts with strong acids, such as

10872-475: Is that of main group elements. A 2003 survey of chemistry books showed that they were treated as either transition metals or main group elements on about a 50/50 basis. The IUPAC Red Book notes that although the group 3−12 elements are commonly referred to as the transition elements, the group 12 elements are not always included. The group 12 elements do not satisfy the IUPAC Gold Book definition of

11023-416: Is that of the preceding noble gas , whereas those of its heavier congeners gallium , indium , thallium , and nihonium also include a filled d-subshell and in some cases a filled f-subshell. Hence, the inner electrons of aluminium shield the valence electrons almost completely, unlike those of aluminium's heavier congeners. As such, aluminium is the most electropositive metal in its group, and its hydroxide

11174-433: Is the eighteenth most abundant nucleus in the universe. It is created almost entirely after fusion of carbon in massive stars that will later become Type II supernovas : this fusion creates Mg, which upon capturing free protons and neutrons, becomes aluminium. Some smaller quantities of Al are created in hydrogen burning shells of evolved stars, where Mg can capture free protons. Essentially all aluminium now in existence

11325-435: Is typical of transition metal compounds. The B-subgroup metals can be subdivided into pseudo metals and hybrid metals . The pseudo metals (groups 12 and 13, including boron) are said to behave more like true metals (groups 1 to 11) than non-metals. The hybrid metals As, Sb, Bi, Te, Po, At — which other authors would call metalloids — partake about equally the properties of both. The pseudo metals can be considered related to

11476-480: Is usually classified as a nonmetal or a metalloid, has been predicted to have a metallic crystalline structure. If so, it would be a post-transition metal. Elements 112–118 ( copernicium , nihonium , flerovium , moscovium , livermorium , tennessine , and oganesson ) may be post-transition metals; insufficient quantities of them have been synthesized to allow sufficient investigation of their actual physical and chemical properties. The diminished metallic nature of

11627-689: Is weakly amphoteric, as is the congener sulfide HgS. It forms anionic thiomercurates (such as Na 2 HgS 2 and BaHgS 3 ) in strongly basic solutions. It forms or is a part of Zintl phases such as NaHg and K 8 In 10 Hg. Mercury is a relatively inert metal, showing little oxide formation at room temperature. Copernicium is expected to be a liquid at room temperature, although experiments have so far not succeeded in determining its boiling point with sufficient precision to prove this. Like its lighter congener mercury, many of its singular properties stem from its closed-shell d s electron configuration as well as strong relativistic effects. Its cohesive energy

11778-411: Is well tolerated by plants and animals. Because of the abundance of these salts, the potential for a biological role for them is of interest, and studies are ongoing. Of aluminium isotopes, only Al is stable. This situation is common for elements with an odd atomic number. It is the only primordial aluminium isotope, i.e. the only one that has existed on Earth in its current form since

11929-459: The -ium spelling as primary, and they list both where it is appropriate. The production of aluminium starts with the extraction of bauxite rock from the ground. The bauxite is processed and transformed using the Bayer process into alumina , which is then processed using the Hall–Héroult process , resulting in the final aluminium. Post-transition metal The metallic elements in

12080-455: The Friedel–Crafts reactions . Aluminium trichloride has major industrial uses involving this reaction, such as in the manufacture of anthraquinones and styrene ; it is also often used as the precursor for many other aluminium compounds and as a reagent for converting nonmetal fluorides into the corresponding chlorides (a transhalogenation reaction ). Aluminium forms one stable oxide with

12231-475: The London Metal Exchange , the oldest industrial metal exchange in the world, in 1978. The output continued to grow: the annual production of aluminium exceeded 50,000,000 metric tons in 2013. The real price for aluminium declined from $ 14,000 per metric ton in 1900 to $ 2,340 in 1948 (in 1998 United States dollars). Extraction and processing costs were lowered over technological progress and

12382-475: The aluminum spelling in his American Dictionary of the English Language . In the 1830s, the -um spelling gained usage in the United States; by the 1860s, it had become the more common spelling there outside science. In 1892, Hall used the -um spelling in his advertising handbill for his new electrolytic method of producing the metal, despite his constant use of the -ium spelling in all

12533-423: The chemical formula Al 2 O 3 , commonly called alumina . It can be found in nature in the mineral corundum , α-alumina; there is also a γ-alumina phase. Its crystalline form, corundum, is very hard ( Mohs hardness 9), has a high melting point of 2,045 °C (3,713 °F), has very low volatility, is chemically inert, and a good electrical insulator, it is often used in abrasives (such as toothpaste), as

12684-551: The interstellar gas ; if the original Al were still present, gamma ray maps of the Milky Way would be brighter. Overall, the Earth is about 1.59% aluminium by mass (seventh in abundance by mass). Aluminium occurs in greater proportion in the Earth's crust than in the universe at large. This is because aluminium easily forms the oxide and becomes bound into rocks and stays in the Earth's crust , while less reactive metals sink to

12835-510: The periodic table located between the transition metals to their left and the chemically weak nonmetallic metalloids to their right have received many names in the literature, such as post-transition metals , poor metals , other metals , p-block metals and chemically weak metals . The most common name, post-transition metals , is generally used in this article. Physically, these metals are soft (or brittle), have poor mechanical strength, and usually have melting points lower than those of

12986-481: The ' lanthanide contraction '. Relativistic effects also "increase the binding energy", and hence ionisation energy, of the electrons in "the 6s shell in gold and mercury, and the 6p shell in subsequent elements of period 6." Platinum is a moderately hard metal (MH 3.5) of low mechanical strength, with a close-packed face-centred cubic structure (BCN 12). Compared to other metals in this category, it has an unusually high melting point (2042 K v 1338 for gold). Platinum

13137-453: The +2 and +4 oxidation states, similar to platinum. Darmstadtium(IV) oxide (DsO 2 ) should be amphoteric, and darmstadtium(II) oxide (DsO) basic, exactly analogous to platinum. There should also be a +6 oxidation state, similar to platinum. Darmstadtium should be a very noble metal: the standard reduction potential for the Ds /Ds couple is expected to be +1.7 V, more than the +1.52 V for

13288-516: The +3 oxidation state should be reachable. Because of the shell closure at flerovium caused by spin-orbit coupling, nihonium is also one 7p electron short of a closed shell and would hence form a −1 oxidation state; in both the +1 and −1 oxidation states, nihonium should show more similarities to astatine than thallium. The Nh ion is expected to also have some similarities to the Ag ion, particularly in its propensity for complexation. Nihonium oxide (Nh 2 O)

13439-474: The 3.6 L engine. This engine features upgrades to the variable valve timing (VVT) system, two-stage variable valve lift (VVL), a new intake manifold , new valve springs, new piston rings , new fuel injectors , new ignition coils , a cooled Exhaust gas recirculation system, lower internal friction and lower weight. It also features a higher compression ratio, increased from 10.2:1 to 11.3:1. These improvements increase power as well as efficiency, however

13590-526: The 5th century BCE. The ancients are known to have used alum as a dyeing mordant and for city defense. After the Crusades , alum, an indispensable good in the European fabric industry, was a subject of international commerce; it was imported to Europe from the eastern Mediterranean until the mid-15th century. The nature of alum remained unknown. Around 1530, Swiss physician Paracelsus suggested alum

13741-420: The 7p subshell is a "partial role reversal" of groups 14 and 18. Due to the immense polarisability of oganesson, it is expected that not only oganesson(II) fluoride but also oganesson(IV) fluoride should be predominantly ionic, involving the formation of Og and Og cations. Oganesson(II) oxide (OgO) and oganesson(IV) oxide (OgO 2 ) are both expected to be amphoteric, similar to the oxides of tin. Superficially,

13892-522: The 7p subshell, so that its 7s 7p 1/2 valence configuration forms a quasi-closed shell similar to those of mercury and copernicium. Solid flerovium should have a face-centered cubic structure and be a rather dense metal, with a density of around 14 g/cm . Flerovium is expected to have a standard electrode potential of +0.9 V for the Fl /Fl couple. Flerovium oxide (FlO) is expected to be amphoteric, forming anionic flerovates in basic solutions. Arsenic

14043-457: The 7s subshell, roentgenium is expected to have a full s-subshell and a partially filled d-subshell, instead of the free s-electron and full d-subshell of copper, silver, and gold. On the group 12 metals (zinc, cadmium and mercury), Smith observed that, "Textbook writers have always found difficulty in dealing with these elements." There is an abrupt and significant reduction in physical metallic character from group 11 to group 12. Their chemistry

14194-472: The Al–Zn–Mg class. Aluminium has a high chemical affinity to oxygen, which renders it suitable for use as a reducing agent in the thermite reaction. A fine powder of aluminium reacts explosively on contact with liquid oxygen ; under normal conditions, however, aluminium forms a thin oxide layer (~5 nm at room temperature) that protects the metal from further corrosion by oxygen, water, or dilute acid,

14345-466: The Au /Au couple. The group 11 metals are typically categorised as transition metals given they can form ions with incomplete d-shells. Physically, they have the relatively low melting points and high electronegativity values associated with post-transition metals. "The filled d subshell and free s electron of Cu, Ag, and Au contribute to their high electrical and thermal conductivity . Transition metals to

14496-537: The B-subgroup metals are the metals in Groups IB to VIIB of the periodic table, corresponding to groups 11 to 17 using current IUPAC nomenclature. Practically, the group 11 metals (copper, silver and gold) are ordinarily regarded as transition metals (or sometimes as coinage metals, or noble metals) whereas the group 12 metals (zinc, cadmium, and mercury) may or may not be treated as B-subgroup metals depending on if

14647-527: The Dodge Challenger. Single and Twin-turbocharged variants had been planned for 2015. These engines were projected to produce around 420 and 370 hp (313 and 276 kW; 426 and 375 PS), respectively. Direct injection was also planned. Due to the new ownership structure, Fiat has obtained the right to use these engines, and had adopted them in the larger models of Lancia and Fiat brands. For 2016, FCA released an updated version of

14798-418: The United States dollar, and alumina prices. The BRIC countries' combined share in primary production and primary consumption grew substantially in the first decade of the 21st century. China is accumulating an especially large share of the world's production thanks to an abundance of resources, cheap energy, and governmental stimuli; it also increased its consumption share from 2% in 1972 to 40% in 2010. In

14949-514: The United States, Western Europe, and Japan, most aluminium was consumed in transportation, engineering, construction, and packaging. In 2021, prices for industrial metals such as aluminium have soared to near-record levels as energy shortages in China drive up costs for electricity. The names aluminium and aluminum are derived from the word alumine , an obsolete term for alumina , the primary naturally occurring oxide of aluminium . Alumine

15100-455: The Zintl phases BaPt, Ba 3 Pt 2 and Ba 2 Pt, being the first (unambiguous) transition metal to do so. Darmstadtium should be similar to its lighter homologue platinum. It is expected to have a close-packed body-centered cubic structure. It should be a very dense metal, with a density of 26–27 g/cm surpassing all stable elements. Darmstadtium chemistry is expected to be dominated by

15251-578: The aluminium atoms have tetrahedral four-coordination and the other half have trigonal bipyramidal five-coordination. Four pnictides – aluminium nitride (AlN), aluminium phosphide (AlP), aluminium arsenide (AlAs), and aluminium antimonide (AlSb) – are known. They are all III-V semiconductors isoelectronic to silicon and germanium , all of which but AlN have the zinc blende structure. All four can be made by high-temperature (and possibly high-pressure) direct reaction of their component elements. Aluminium alloys well with most other metals (with

15402-449: The astatide formed with mercury as Hg(OH)At. Tennessine , despite being in the halogen column of the periodic table, is expected to go even further towards metallicity than astatine due to its small electron affinity. The −1 state should not be important for tennessine and its major oxidation states should be +1 and +3, with +3 more stable: Ts is expected to behave similarly to Au in halide media. As such, tennessine oxide (Ts 2 O 3 )

15553-443: The case of aluminium , tin, and bismuth, respectively). They can also form Zintl phases (half-metallic compounds formed between highly electropositive metals and moderately electronegative metals or metalloids). The post-transition metals are located on the periodic table between the transition metals to their left and the chemically weak nonmetallic metalloids or nonmetals to their right. Generally included in this category are:

15704-436: The characteristic physical properties of a post-transition metal, with longer-than-expected interatomic distances. Furthermore, as Al is a small and highly charged cation, it is strongly polarizing and bonding in aluminium compounds tends towards covalency ; this behavior is similar to that of beryllium (Be ), and the two display an example of a diagonal relationship . The underlying core under aluminium's valence shell

15855-419: The coordination numbers are lower. The other trihalides are dimeric or polymeric with tetrahedral four-coordinate aluminium centers. Aluminium trichloride (AlCl 3 ) has a layered polymeric structure below its melting point of 192.4 °C (378 °F) but transforms on melting to Al 2 Cl 6 dimers. At higher temperatures those increasingly dissociate into trigonal planar AlCl 3 monomers similar to

16006-428: The core. In the Earth's crust, aluminium is the most abundant metallic element (8.23% by mass ) and the third most abundant of all elements (after oxygen and silicon). A large number of silicates in the Earth's crust contain aluminium. In contrast, the Earth's mantle is only 2.38% aluminium by mass. Aluminium also occurs in seawater at a concentration of 2 μg/kg. Because of its strong affinity for oxygen, aluminium

16157-497: The energy released by the decay of Al was responsible for the melting and differentiation of some asteroids after their formation 4.55 billion years ago. The remaining isotopes of aluminium, with mass numbers ranging from 21 to 43, all have half-lives well under an hour. Three metastable states are known, all with half-lives under a minute. An aluminium atom has 13 electrons, arranged in an electron configuration of [ Ne ] 3s 3p , with three electrons beyond

16308-649: The engine design, but have not been implemented from the factory, remaining "on the shelf" as of 2016. Insiders initially reported that the engine would come in four basic sizes (3.0, 3.3, 3.6, and 4.0 L), each offered in various states of tune . The 3.3 L and 4.0 L have been dropped from the list and a 3.2L added, while Fiat's investor website, as of December 2011, specifies the 3.0 L with Fiat's MultiAir technology. The 3.6 L engine itself has different power ratings in different vehicles, and has higher output 305 hp (227 kW; 309 PS) and 269 pound force-feet (365 N⋅m) of torque when applied in

16459-478: The exception of most alkali metals and group 13 metals) and over 150 intermetallics with other metals are known. Preparation involves heating fixed metals together in certain proportion, followed by gradual cooling and annealing . Bonding in them is predominantly metallic and the crystal structure primarily depends on efficiency of packing. There are few compounds with lower oxidation states. A few aluminium(I) compounds exist: AlF, AlCl, AlBr, and AlI exist in

16610-520: The fact that its nuclei are much lighter, while difference in the unit cell size does not compensate for this difference. The only lighter metals are the metals of groups 1 and 2 , which apart from beryllium and magnesium are too reactive for structural use (and beryllium is very toxic). Aluminium is not as strong or stiff as steel, but the low density makes up for this in the aerospace industry and for many other applications where light weight and relatively high strength are crucial. Pure aluminium

16761-442: The formation of the planet. It is therefore a mononuclidic element and its standard atomic weight is virtually the same as that of the isotope. This makes aluminium very useful in nuclear magnetic resonance (NMR), as its single stable isotope has a high NMR sensitivity. The standard atomic weight of aluminium is low in comparison with many other metals. All other isotopes of aluminium are radioactive . The most stable of these

16912-453: The former Chrysler Corporation, which dates back to 1963. The Pentastar engines are made in three different factories: Dundee Engine Plant , Trenton Engine Plant and Saltillo South Engine Plant . The Pentastar engine was introduced at the 2009 New York Auto Show . The engine design allows the use of E85 or 87 octane fuel and features dual variable valve timing. Forced induction , and cylinder deactivation options were engineered into

17063-730: The gas phase after explosion and in stellar absorption spectra. More thoroughly investigated are compounds of the formula R 4 Al 2 which contain an Al–Al bond and where R is a large organic ligand . A variety of compounds of empirical formula AlR 3 and AlR 1.5 Cl 1.5 exist. The aluminium trialkyls and triaryls are reactive, volatile, and colorless liquids or low-melting solids. They catch fire spontaneously in air and react with water, thus necessitating precautions when handling them. They often form dimers, unlike their boron analogues, but this tendency diminishes for branched-chain alkyls (e.g. Pr , Bu , Me 3 CCH 2 ); for example, triisobutylaluminium exists as an equilibrium mixture of

17214-453: The gaseous phase when the respective trihalide is heated with aluminium, and at cryogenic temperatures. A stable derivative of aluminium monoiodide is the cyclic adduct formed with triethylamine , Al 4 I 4 (NEt 3 ) 4 . Al 2 O and Al 2 S also exist but are very unstable. Very simple aluminium(II) compounds are invoked or observed in the reactions of Al metal with oxidants. For example, aluminium monoxide , AlO, has been detected in

17365-485: The group 10 metal platinum ; the group 11 coinage metals copper , silver and gold ; and, more often, the group 12 metals zinc , cadmium and mercury . Similarly, some elements otherwise counted as metalloids or nonmetals are sometimes instead counted as post-transition metals namely germanium , arsenic , selenium , antimony , tellurium , and polonium (of which germanium, arsenic, antimony, and tellurium are usually considered to be metalloids). Astatine , which

17516-581: The group 13–16 metals in periods 4–6 namely gallium , indium and thallium , tin and lead , bismuth , and polonium ; and aluminium , a group 13 metal in period 3. They can be seen at the bottom right in the accompanying plot of electronegativity values and melting points. The boundaries of the category are not necessarily sharp as there is some overlapping of properties with adjacent categories (as occurs with classification schemes generally). Some elements otherwise counted as transition metals are sometimes instead counted as post-transition metals namely

17667-646: The halides, nitrate , and sulfate . For similar reasons, anhydrous aluminium salts cannot be made by heating their "hydrates": hydrated aluminium chloride is in fact not AlCl 3 ·6H 2 O but [Al(H 2 O) 6 ]Cl 3 , and the Al–O bonds are so strong that heating is not sufficient to break them and form Al–Cl bonds instead: All four trihalides are well known. Unlike the structures of the three heavier trihalides, aluminium fluoride (AlF 3 ) features six-coordinate aluminium, which explains its involatility and insolubility as well as high heat of formation . Each aluminium atom

17818-432: The lead atoms. It forms a semi-covalent dioxide PbO 2 ; a covalently bonded sulfide PbS; covalently bonded halides; and a range of covalently bonded organolead compounds such as the lead(II) mercaptan Pb(SC 2 H 5 ) 2 , lead tetra-acetate Pb(CH 3 CO 2 ) 4 , and the once common, anti-knock additive, tetra-ethyl lead (CH 3 CH 2 ) 4 Pb . The oxide of lead in its preferred oxidation state (PbO; +2)

17969-444: The left of group 11 experience interactions between s electrons and the partially filled d subshell that lower electron mobility." Chemically, the group 11 metals in their +1 valence states show similarities to other post-transition metals; they are occasionally classified as such. Copper is a soft metal (MH 2.5–3.0) with low mechanical strength. It has a close-packed face-centred cubic structure (BCN 12). Copper behaves like

18120-433: The low-pressure polymerization of ethene and propene . There are also some heterocyclic and cluster organoaluminium compounds involving Al–N bonds. The industrially most important aluminium hydride is lithium aluminium hydride (LiAlH 4 ), which is used as a reducing agent in organic chemistry . It can be produced from lithium hydride and aluminium trichloride . The simplest hydride, aluminium hydride or alane,

18271-529: The metal remained rare; its cost exceeded that of gold. The first industrial production of aluminium was established in 1856 by French chemist Henri Etienne Sainte-Claire Deville and companions. Deville had discovered that aluminium trichloride could be reduced by sodium, which was more convenient and less expensive than potassium, which Wöhler had used. Even then, aluminium was still not of great purity and produced aluminium differed in properties by sample. Because of its electricity-conducting capacity, aluminium

18422-655: The metal to be isolated from alum was alumium , which Davy suggested in an 1808 article on his electrochemical research, published in Philosophical Transactions of the Royal Society . It appeared that the name was created from the English word alum and the Latin suffix -ium ; but it was customary then to give elements names originating in Latin, so this name was not adopted universally. This name

18573-465: The metal with many uses at the time. During World War I , major governments demanded large shipments of aluminium for light strong airframes; during World War II , demand by major governments for aviation was even higher. By the mid-20th century, aluminium had become a part of everyday life and an essential component of housewares. In 1954, production of aluminium surpassed that of copper , historically second in production only to iron, making it

18724-491: The metal. Almost all metallic aluminium is produced from the ore bauxite (AlO x (OH) 3–2 x ). Bauxite occurs as a weathering product of low iron and silica bedrock in tropical climatic conditions. In 2017, most bauxite was mined in Australia, China, Guinea, and India. The history of aluminium has been shaped by usage of alum . The first written record of alum, made by Greek historian Herodotus , dates back to

18875-485: The monomer and dimer. These dimers, such as trimethylaluminium (Al 2 Me 6 ), usually feature tetrahedral Al centers formed by dimerization with some alkyl group bridging between both aluminium atoms. They are hard acids and react readily with ligands, forming adducts. In industry, they are mostly used in alkene insertion reactions, as discovered by Karl Ziegler , most importantly in "growth reactions" that form long-chain unbranched primary alkenes and alcohols, and in

19026-402: The most electronegative ligands. Livermorium(II) oxide (LvO) should be basic and livermorium(IV) oxide (LvO 2 ) should be amphoteric, analogous to polonium. Astatine is a radioactive element that has never been seen; a visible quantity would immediately be vaporised due to its intense radioactivity. It may be possible to prevent this with sufficient cooling. Astatine is commonly regarded as

19177-506: The most produced non-ferrous metal . During the mid-20th century, aluminium emerged as a civil engineering material, with building applications in both basic construction and interior finish work, and increasingly being used in military engineering, for both airplanes and land armor vehicle engines. Earth's first artificial satellite , launched in 1957, consisted of two separate aluminium semi-spheres joined and all subsequent space vehicles have used aluminium to some extent. The aluminium can

19328-474: The new version no longer supports flex-fuel capability. Aluminium Aluminium (or aluminum in North American English ) is a chemical element ; it has symbol   Al and atomic number  13. Aluminium has a density lower than that of other common metals , about one-third that of steel . It has a great affinity towards oxygen , forming a protective layer of oxide on

19479-614: The next decade, the -um spelling dominated American usage. In 1925, the American Chemical Society adopted this spelling. The International Union of Pure and Applied Chemistry (IUPAC) adopted aluminium as the standard international name for the element in 1990. In 1993, they recognized aluminum as an acceptable variant; the most recent 2005 edition of the IUPAC nomenclature of inorganic chemistry also acknowledges this spelling. IUPAC official publications use

19630-464: The only Group 13 elements to react with air at room temperature, slowly forming the amphoteric oxide Tl 2 O 3 . It forms anionic thallates such as Tl 3 TlO 3 , Na 3 Tl(OH) 6 , NaTlO 2 , and KTlO 2 , and is present as the Tl thallide anion in the compound CsTl. Thallium forms Zintl phases, such as Na 2 Tl, Na 2 K 21 Tl 19 , CsTl and Sr 5 Tl 3 H. Nihonium is expected to have

19781-407: The oxidation state 3+. The coordination number of such compounds varies, but generally Al is either six- or four-coordinate. Almost all compounds of aluminium(III) are colorless. In aqueous solution, Al exists as the hexaaqua cation [Al(H 2 O) 6 ] , which has an approximate K a of 10 . Such solutions are acidic as this cation can act as a proton donor and progressively hydrolyze until

19932-460: The patents he filed between 1886 and 1903. It is unknown whether this spelling was introduced by mistake or intentionally, but Hall preferred aluminum since its introduction because it resembled platinum , the name of a prestigious metal. By 1890, both spellings had been common in the United States, the -ium spelling being slightly more common; by 1895, the situation had reversed; by 1900, aluminum had become twice as common as aluminium ; in

20083-619: The post-transition metals is largely attributable to the increase in nuclear charge going across the periodic table, from left to right. The increase in nuclear charge is partially offset by an increasing number of electrons but as these are spatially distributed each extra electron does not fully screen each successive increase in nuclear charge, and the latter therefore dominates. With some irregularities, atomic radii contract, ionisation energies increase, fewer electrons become available for metallic bonding, and "ions [become] smaller and more polarizing and more prone to covalency." This phenomenon

20234-423: The respective hydrogen chalcogenide . As aluminium is a small atom relative to these chalcogens, these have four-coordinate tetrahedral aluminium with various polymorphs having structures related to wurtzite , with two-thirds of the possible metal sites occupied either in an orderly (α) or random (β) fashion; the sulfide also has a γ form related to γ-alumina, and an unusual high-temperature hexagonal form where half

20385-402: The same structure as diamond, silicon and germanium (BCN 4). This transformation causes ordinary tin to crumble and disintegrate since, as well as being brittle, grey tin occupies more volume due to having a less efficient crystalline packing structure. Tin forms Zintl phases such as Na 4 Sn, BaSn, K 8 Sn 25 and Ca 31 Sn 20 . It has good corrosion resistance in air on account of forming

20536-485: The scale of the economies. However, the need to exploit lower-grade poorer quality deposits and the use of fast increasing input costs (above all, energy) increased the net cost of aluminium; the real price began to grow in the 1970s with the rise of energy cost. Production moved from the industrialized countries to countries where production was cheaper. Production costs in the late 20th century changed because of advances in technology, lower energy prices, exchange rates of

20687-408: The structure of BCl 3 . Aluminium tribromide and aluminium triiodide form Al 2 X 6 dimers in all three phases and hence do not show such significant changes of properties upon phase change. These materials are prepared by treating aluminium with the halogen. The aluminium trihalides form many addition compounds or complexes; their Lewis acidic nature makes them useful as catalysts for

20838-401: The surface when exposed to air. Aluminium visually resembles silver , both in its color and in its great ability to reflect light. It is soft, nonmagnetic , and ductile . It has one stable isotope, Al, which is highly abundant, making aluminium the twelfth-most common element in the universe. The radioactivity of Al leads to it being used in radiometric dating . Chemically, aluminium

20989-600: The transition metals are taken to end at group 11 or group 12. The 'B' nomenclature (as in Groups IB, IIB, and so on) was superseded in 1988 but is still occasionally encountered in more recent literature. The B-subgroup metals show nonmetallic properties; this is particularly apparent in moving from group 12 to group 16. Although the group 11 metals have normal close-packed metallic structures they show an overlap in chemical properties. In their +1 compounds (the stable state for silver; less so for copper) they are typical B-subgroup metals. In their +2 and +3 states their chemistry

21140-455: The transition metals. Being close to the metal-nonmetal border , their crystalline structures tend to show covalent or directional bonding effects, having generally greater complexity or fewer nearest neighbours than other metallic elements. Chemically, they are characterised—to varying degrees—by covalent bonding tendencies, acid-base amphoterism and the formation of anionic species such as aluminates , stannates , and bismuthates (in

21291-536: The two therefore look similar. Aluminium is also good at reflecting solar radiation , although prolonged exposure to sunlight in air adds wear to the surface of the metal; this may be prevented if aluminium is anodized , which adds a protective layer of oxide on the surface. The density of aluminium is 2.70 g/cm , about 1/3 that of steel, much lower than other commonly encountered metals, making aluminium parts easily identifiable through their lightness. Aluminium's low density compared to most other metals arises from

21442-456: The −1, +1, and +5 valence states should also exist, exactly analogous to gold. Roentgenium is similarly expected to be a very noble metal: the standard reduction potential for the Rg /Rg couple is expected to be +1.9 V, more than the +1.52 V for the Au /Au couple. The [Rg(H 2 O) 2 ] cation is expected to be the softest among the metal cations. Due to relativistic stabilisation of

21593-421: Was a crucial strategic resource for aviation . In 1954, aluminium became the most produced non-ferrous metal , surpassing copper . In the 21st century, most aluminium was consumed in transportation, engineering, construction, and packaging in the United States, Western Europe, and Japan. Despite its prevalence in the environment, no living organism is known to metabolize aluminium salts , but this aluminium

21744-461: Was a salt of an earth of alum. In 1595, German doctor and chemist Andreas Libavius experimentally confirmed this. In 1722, German chemist Friedrich Hoffmann announced his belief that the base of alum was a distinct earth. In 1754, German chemist Andreas Sigismund Marggraf synthesized alumina by boiling clay in sulfuric acid and subsequently adding potash . Attempts to produce aluminium date back to 1760. The first successful attempt, however,

21895-494: Was borrowed from French, which in turn derived it from alumen , the classical Latin name for alum , the mineral from which it was collected. The Latin word alumen stems from the Proto-Indo-European root *alu- meaning "bitter" or "beer". British chemist Humphry Davy , who performed a number of experiments aimed to isolate the metal, is credited as the person who named the element. The first name proposed for

22046-422: Was completed in 1824 by Danish physicist and chemist Hans Christian Ørsted . He reacted anhydrous aluminium chloride with potassium amalgam , yielding a lump of metal looking similar to tin. He presented his results and demonstrated a sample of the new metal in 1825. In 1827, German chemist Friedrich Wöhler repeated Ørsted's experiments but did not identify any aluminium. (The reason for this inconsistency

22197-496: Was criticized by contemporary chemists from France, Germany, and Sweden, who insisted the metal should be named for the oxide, alumina, from which it would be isolated. The English name alum does not come directly from Latin, whereas alumine / alumina obviously comes from the Latin word alumen (upon declension , alumen changes to alumin- ). One example was Essai sur la Nomenclature chimique (July 1811), written in French by

22348-517: Was initiated by French chemist Henri Étienne Sainte-Claire Deville in 1856. Aluminium became much more available to the public with the Hall–Héroult process developed independently by French engineer Paul Héroult and American engineer Charles Martin Hall in 1886, and the mass production of aluminium led to its extensive use in industry and everyday life. In the First and Second World Wars, aluminium

22499-418: Was invented in 1956 and employed as a storage for drinks in 1958. Throughout the 20th century, the production of aluminium rose rapidly: while the world production of aluminium in 1900 was 6,800 metric tons, the annual production first exceeded 100,000 metric tons in 1916; 1,000,000 tons in 1941; 10,000,000 tons in 1971. In the 1970s, the increased demand for aluminium made it an exchange commodity; it entered

22650-433: Was only discovered in 1921.) He conducted a similar experiment in the same year by mixing anhydrous aluminium chloride with potassium and produced a powder of aluminium. In 1845, he was able to produce small pieces of the metal and described some physical properties of this metal. For many years thereafter, Wöhler was credited as the discoverer of aluminium. As Wöhler's method could not yield great quantities of aluminium,

22801-580: Was used as the cap of the Washington Monument , completed in 1885. The tallest building in the world at the time, the non-corroding metal cap was intended to serve as a lightning rod peak. The first industrial large-scale production method was independently developed in 1886 by French engineer Paul Héroult and American engineer Charles Martin Hall ; it is now known as the Hall–Héroult process . The Hall–Héroult process converts alumina into metal. Austrian chemist Carl Joseph Bayer discovered

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