Silicate minerals are rock-forming minerals made up of silicate groups. They are the largest and most important class of minerals and make up approximately 90 percent of Earth's crust. In mineralogy, the crystalline forms of silica (SiO2) are usually considered to be tectosilicates, and they are classified as such in the Dana classification system (75.1). However, the Nickel–Strunz classification categorizes them as oxide minerals (4.DA). Silica is found in nature as the mineral quartz and its polymorphs. On Earth, a wide variety of silicate minerals occur in an even wider range of combinations as a result of the processes that have been forming and re-working the crust for billions of years. These processes include partial melting, crystallization, fractionation, metamorphism, weathering, and diagenesis.
Living organisms also contribute to this geologic cycle. For example, a type of plankton known as diatoms construct their exoskeletons ("frustules") from silica extracted from seawater. The frustules of dead diatoms are a major constituent of deep ocean sediment, and of diatomaceous earth.
General structure A silicate mineral is generally an inorganic compound consisting of subunits with the formula [SiO2+n]2n−. Although depicted as such, the description of silicates as anions is a simplification. Balancing the charges of the silicate anions are metal cations, Mx+. Typical cations are Mg2+, Fe2+, and Na+. The Si-O-M linkage between the silicates and the metals are strong, polar-covalent bonds. Silicate anions ([SiO2+n]2n−) are invariably colorless, or when crushed to a fine powder, white. The colors of silicate minerals arise from the metal component, commonly iron. In most silicate minerals, silicon is tetrahedral, being surrounded by four oxides. The coordination number of the oxides is variable except when it bridges two silicon centers, in which case the oxide has a coordination number of two. Some silicon centers may be replaced by atoms of other elements, still bound to the four corner oxygen corners. If the substituted atom is not normally tetravalent, it usually contributes extra charge to the anion, which then requires extra cations. For example, in the mineral orthoclase [KAlSi3O8]n, the anion is a tridimensional network of tetrahedra in which all oxygen corners are shared. If all tetrahedra had silicon centers, the anion would be just neutral silica [SiO2]n. Replacement of one in every four silicon atoms by an aluminum atom results in the anion [AlSi3O−8]n, whose charge is neutralized by the potassium cations K+.
Main groups In mineralogy, silicate minerals are classified into seven major groups according to the structure of their silicate anion:
Tectosilicates can only have additional cations if some of the silicon is replaced by an atom of lower valence such as aluminum. Al for Si substitution is common.
Nesosilicates or orthosilicates
Nesosilicates (from Greek νῆσος nēsos 'island'), or orthosilicates, have the orthosilicate ion, present as isolated (insular) [SiO4]4− tetrahedra connected only by interstitial cations. The Nickel–Strunz classification is 09.A –examples include:
Phenakite – Be2SiO4 Willemite – Zn2SiO4 Olivine group Forsterite – Mg2SiO4 Fayalite – Fe2SiO4 Tephroite – Mn2SiO4 Garnet group Pyrope – Mg3Al2(SiO4)3 Almandine – Fe3Al2(SiO4)3 Spessartine – Mn3Al2(SiO4)3 Grossular – Ca3Al2(SiO4)3 Andradite – Ca3Fe2(SiO4)3 Uvarovite – Ca3Cr2(SiO4)3 Hydrogrossular – Ca3Al2Si2O8(SiO4)3−m(OH)4m Zircon group Zircon – ZrSiO4 Thorite – (Th,U)SiO4 Hafnon – (Hf,Zr)SiO4 Wollastonite group (pyroxenoid group) Wollastonite – CaSiO₃ Pectolite – NaCa₂Si₃O₈(OH) Serandite – Na(Mn²⁺,Ca)₂Si₃O₈(OH) Nambulite – LiMn₄Si₅O₁₄(OH) Fowlerite – (Ca,Mn)₂Si₃O₈(OH)
Al2SiO5 group Andalusite – Al2SiO5 Kyanite – Al2SiO5 Sillimanite – Al2SiO5 Dumortierite – Al6.5–7BO3(SiO4)3(O,OH)3 Topaz – Al2SiO4(F,OH)2 Staurolite – Fe2Al9(SiO4)4(O,OH)2 Humite group – (Mg,Fe)7(SiO4)3(F,OH)2 Norbergite – Mg3(SiO4)(F,OH)2 Chondrodite – Mg5(SiO4)2(F,OH)2 Humite – Mg7(SiO4)3(F,OH)2 Clinohumite – Mg9(SiO4)4(F,OH)2 Datolite – CaBSiO4(OH) Titanite – CaTiSiO5 Chloritoid – (Fe,Mg,Mn)2Al4Si2O10(OH)4 Mullite (aka Porcelainite) – Al6Si2O13
Sorosilicates
Sorosilicates (from Greek σωρός sōros 'heap, mound') have isolated pyrosilicate anions Si2O6−7, consisting of double tetrahedra with a shared oxygen vertex—a silicon:oxygen ratio of 2:7. The Nickel–Strunz classification is 09.B. Examples include:
Thortveitite – (Sc,Y)2(Si2O7) Hemimorphite (calamine) – Zn4(Si2O7)(OH)2·H2O Lawsonite – CaAl2(Si2O7)(OH)2·H2O Axinite – (Ca,Fe,Mn)3Al2(BO3)(Si4O12)(OH) Ilvaite – CaFeII2FeIIIO(Si2O7)(OH) Epidote group (has both (SiO4)4− and (Si2O7)6− groups} Epidote – Ca2(Al,Fe)3O(SiO4)(Si2O7)(OH) Zoisite – Ca2Al3O(SiO4)(Si2O7)(OH) Tanzanite – Ca2Al3O(SiO4)(Si2O7)(OH) Clinozoisite – Ca2Al3O(SiO4)(Si2O7)(OH) Allanite – Ca(Ce,La,Y,Ca)Al2(FeII,FeIII)O(SiO4)(Si2O7)(OH) Dollaseite-(Ce) – CaCeMg2AlSi3O11F(OH) Vesuvianite (idocrase) – Ca10(Mg,Fe)2Al4(SiO4)5(Si2O7)2(OH)4
Cyclosilicates
Cyclosilicates (from Greek κύκλος kýklos 'circle'), or ring silicates, have three or more tetrahedra linked in a ring. The general formula is (SixO3x)2x−, where one or more silicon atoms can be replaced by other 4-coordinated atom(s). The silicon:oxygen ratio is 1:3. Double rings have the formula (Si2xO5x)2x− or a 2:5 ratio. The Nickel–Strunz classification is 09.C. Possible ring sizes include:
Some example minerals are:
3-member single ring Benitoite – BaTi(Si3O9) 4-member single ring Papagoite – CaCuAlSi2O6(OH)3. 6-member single ring Beryl – Be3Al2(Si6O18) Bazzite – Be3Sc2(Si6O18) Sugilite – KNa2(Fe,Mn,Al)2Li3Si12O30 Tourmaline – (Na,Ca)(Al,Li,Mg)3–(Al,Fe,Mn)6(Si6O18)(BO3)3(OH)4 Pezzottaite – Cs(Be2Li)Al2Si6O18 Osumilite – (K,Na)(Fe,Mg)2(Al,Fe)3(Si,Al)12O30 Cordierite – (Mg,Fe)2Al4Si5O18 Sekaninaite – (Fe+2,Mg)2Al4Si5O18 9-member single ring Eudialyte – Na15Ca6(Fe,Mn)3Zr3SiO(O,OH,H2O)3(Si3O9)2(Si9O27)2(OH,Cl)2 6-member double ring Milarite – K2Ca4Al2Be4(Si24O60)H2O The ring in axinite contains two B and four Si tetrahedra and is highly distorted compared to the other 6-member ring cyclosilicates.
Inosilicates
Inosilicates (from Greek ἴς is [genitive: ἰνός inos] 'fibre'), or chain silicates, have interlocking chains of silicate tetrahedra with either SiO3, 1:3 ratio, for single chains or Si4O11, 4:11 ratio, for double chains. The Nickel–Strunz classification is 09.D – examples include:
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