Wollastonite
| Wollastonite | |
|---|---|
 |
|
| General | |
| Category | Silicate mineral |
| Formula (repeating unit) |
Calcium silicate, CaSiO3 |
| Strunz classification | 9.DG.05 |
| Crystal system | Triclinic Monoclinic polytype exists |
| Crystal class | Pinacoidal (1) H-M symbol: (1) |
| Space group | P1 (1A polytype) |
| Unit cell | a = 7.925 Å, b = 7.32 Å, c = 7.065 Å; α = 90.055°, β = 95.217°, γ = 103.42°; Z = 6 |
| Identification | |
| Color | White, colorless or gray |
| Crystal habit | Rare as tabular crystals—commonly massive in lamellar, radiating, compact and fibrous aggregates. |
| Twinning | Common |
| Cleavage | Perfect in two directions at near 90° |
| Fracture | Splintery to uneven |
| Mohs scale hardness | 4.5 to 5.0 |
| Luster | Vitreous or dull to pearly on cleavage surfaces |
| Streak | White |
| Diaphaneity | Transparent to translucent |
| Specific gravity | 2.86–3.09 |
| Optical properties | Biaxial (-) |
| Refractive index | nα = 1.616–1.640 nβ = 1.628–1.650 nγ = 1.631–1.653 |
| Birefringence | δ = 0.015 max |
| 2V angle | Measured: 36° to 60° |
| Melting point | 1540 °C |
| Solubility | Soluble in HCl, insoluble in water |
| References | [1][2][3][4][5] |
Wollastonite is a calcium inosilicate mineral (CaSiO3) that may contain small amounts of iron, magnesium, and manganese substituting for calcium. It is usually white. It forms when impure limestone or dolostone is subjected to high temperature and pressure sometimes in the presence of silica-bearing fluids as in skarns or contact metamorphic rocks. Associated minerals include garnets, vesuvianite, diopside, tremolite, epidote, plagioclase feldspar, pyroxene and calcite. It is named after the English chemist and mineralogist William Hyde Wollaston (1766–1828).
Some of the properties that make wollastonite so useful are its high brightness and whiteness, low moisture and oil absorption, and low volatile content. Wollastonite is used primarily in ceramics, friction products (brakes and clutches), metalmaking, paint filler, and plastics.
Despite its chemical similarity to the compositional spectrum of the pyroxene group of minerals—where magnesium and iron substitution for calcium ends with diopside and hedenbergite respectively—it is structurally very different, with a third SiO4 tetrahedron[6] in the linked chain (as opposed to two in the pyroxenes).
Contents
Production trends[edit]
World production data for wollastonite is not available for many countries and those that are available frequently are 2 to 3 years old. Estimated world production of crude wollastonite ore was in the range of 530,000 to 550,000 tonnes in 2010. World reserves of wollastonite were estimated to exceed 90 million tonnes, with probable reserves of about 270 million tonnes. However, many large deposits have not been surveyed yet.[7]
In 2010, the major producers were China (300,000 tonnes), India (120,000 t), United States (67,000 t), Mexico (30,000 t) and Finland (16,000).[7] Finland has long been a major European supplier of wollastonite, but in 2003 it was joined by Spain with comparable production volumes. In the United States, wollastonite is mined in Willsboro, New York and Gouverneur, New York. Deposits have also been mined commercially in North Western Mexico.[8]
Uses[edit]
Wollastonite has industrial importance worldwide. It is used in many industries, mostly by tile factories which have incorporated it into the manufacturing of ceramic to improve many aspects, and this is due to its fluxing properties, freedom from volatile constituents, whiteness, and acicular particle shape.[9] In ceramics, wollastonite decreases shrinkage and gas evolution during firing, increases green and fired strength, maintains brightness during firing, permits fast firing, and reduces crazing, cracking, and glaze defects. In metallurgical applications, wollastonite serves as a flux for welding, a source for calcium oxide, a slag conditioner, and to protect the surface of molten metal during the continuous casting of steel. As an additive in paint, it improves the durability of the paint film, acts as a pH buffer, improves its resistance to weathering, reduces gloss, reduces pigment consumption, and acts as a flatting and suspending agent. In plastics, wollastonite improves tensile and flexural strength, reduces resin consumption, and improves thermal and dimensional stability at elevated temperatures. Surface treatments are used to improve the adhesion between the wollastonite and the polymers to which it is added. As a substitute for asbestos in floor tiles, friction products, insulating board and panels, paint, plastics, and roofing products, wollastonite is resistant to chemical attack, inert, stable at high temperatures, and improves flexural and tensile strength.[8] In some industries, it is used in different percentages of impurities, such as its use as a fabricator of mineral wool insulation, or as an ornamental building material.[10]
Plastics and rubber applications were estimated to account for 25% to 35% of U.S. sales in 2009, followed by ceramics with 20% to 25%; paint, 10% to 15%; metallurgical applications, 10% to 15%; friction products, 10% to 15%; and miscellaneous, 10% to 15%. Ceramic applications probably account for 30% to 40% of wollastonite sales worldwide, followed by polymers (plastics and rubber) with 30% to 35% of sales, and paint with 10% to 15% of sales. The remaining sales were for construction, friction products, and metallurgical applications. The price of raw wollastonite varied in 2008 between US$80 and US$500 per tonne depending on the country and size and shape of the powder particles.[8]
Substitutes[edit]
The acicular nature of many wollastonite products allows it to compete with other acicular materials, such as ceramic fiber, glass fiber, steel fiber, and several organic fibers, such as aramid, polyethylene, polypropylene, and polytetrafluoroethylene in products where improvements in dimensional stability, flexural modulus, and heat deflection are sought. Wollastonite also competes with several nonfibrous minerals or rocks, such as kaolin, mica, and talc, which are added to plastics to increase flexural strength, and such minerals as barite, calcium carbonate, gypsum, and talc, which impart dimensional stability to plastics. In ceramics, wollastonite competes with carbonates, feldspar, lime, and silica as a source of calcium and silicon. Its use in ceramics depends on the formulation of the ceramic body and the firing method.[7]
Composition[edit]
In a pure CaSiO3, each component forms nearly half of the mineral by weight: 48.3% of CaO and 51.7% of SiO2. In some cases, small amounts of iron (Fe), and manganese (Mn), and lesser amounts of magnesium (Mg) substitute for calcium (Ca) in the mineral formula (e.g., rhodonite).[10] Wollastonite can form a series of solid solutions in the system CaSiO3-FeSiO3, or hydrothermal synthesis of phases in the system MnSiO3-CaSiO3.[9]
Geologic occurrence[edit]
Wollastonite usually occurs as a common constituent of a thermally metamorphosed impure limestone, it also could occur when the silicon is due to metamorphism in contact altered calcareous sediments, or to contamination in the invading igneous rock. In most of these occurrences it is the result of the following reaction between calcite and silica with the loss of carbon dioxide:[9]
- CaCO3 + SiO2 → CaSiO3 + CO2
Wollastonite may also be produced in a diffusion reaction in skarn, it develops when limestone within a sandstone is metamorphosed by a dike, which results in the formation of wollastonite in the sandstone as a result of outward migration of Ca.[9]
Structure[edit]
Wollastonite crystallizes triclinically in space group P1 with the lattice constants a = 7.94 Å, b = 7.32 Å, c = 7.07 Å; α = 90,03°, β = 95,37°, γ = 103,43° and six formula units per unit cell.[11] Wollastonite was once classed structurally among the pyroxene group, because both of these groups have a ratio of Si:O = 1:3. In 1931, Warren and Biscoe showed that the crystal structure of wollastonite differs from minerals of the pyroxene group, and they classified this mineral within a group known as the pyroxenoids.[9] It has been shown that the pyroxenoid chains are more kinked than those of pyroxene group, and exhibit longer repeat distance. The structure of wollastonite contains infinite chains of [SiO4] tetrahedra sharing common vertices, running parallel to the b-axis. The chain motif in wollastonite repeats after three tetrahedra, whereas in pyroxenes only two are needed. The repeat distance in the wollastonite chains is 7.32 Å and equals the length of the crystallographic b-axis.
Molten CaSiO3, maintains a tetrahedral SiO4 local structure, at temperatures up to 2000 ˚C.[12] The nearest neighbour Ca-O coordination decreases from 6.0(2) in the room temperature glass to 5.0(2) in the 1700 ˚C liquid, coincident with an increasing number of longer Ca-O neighbors.[13][14]
Physical and optical properties[edit]
Wollastonite occurs as bladed crystal masses, single crystals can show an acicular particle shape and usually it exhibits a white color, but sometimes cream, grey or very pale green.
The streak of wollastonite is white, its Mohs hardness is 4.5–5 and specific gravity is 2.87–3.09. There are more than one cleavage planes for it, there is a perfect cleavage on {100}, good cleavages on {001}, and {102}, and an imperfect cleavage on {101}. It is common for wollastonite to have a twin axis [010], a composition plane (100), and rarely to have a twin axis [001]. The luster is usually vitreous to pearly. The melting point of wollastonite is about 1540 ˚C.
See also[edit]
References[edit]
This article incorporates public domain material from the United States Geological Survey document: "Wollastonite".
- ^ Wollastonite, Mindat
- ^ Wollastonite, Webmineral
- ^ Wollastonite Mineral galleries
- ^ Wollastonite, Handbook of Mineralogy
- ^ [1]
- ^ William Alexander Deer; Robert Andrew Howie; J. Zussman (1992). An introduction to the rock-forming minerals. Longman Scientific & Technical. ISBN 978-0-470-21809-9.
- ^ a b c Wollastonite, USGS Mineral Commodity Summaries 2011
- ^ a b c Robert L. Virta Wollastonite, USGS 2009 Minerals Yearbook (October 2010)
- ^ a b c d e Deer, Howie and Zussman. Rock Forming Minerals; Single Chain Silicates, Vol. 2A, Second Edition, London, The Geological Society, 1997.
- ^ a b Andrews, R. W. Wollastonite. London, Her Majesty's Stationery Office, 1970.
- ^ Buerger, M. J. (1961). "The crystal structures of wollastonite and pectolite". Proceedings of the National Academy of Sciences. 47 (12): 1884–1888. Bibcode:1961PNAS...47.1884B. doi:10.1073/pnas.47.12.1884. JSTOR 71064.
- ^ Benmore, C.J.; et al. (2010). "Temperature-dependent structural heterogeneity in calcium silicate liquids". Phys. Rev. B (82): 224202. Bibcode:2010PhRvB..82v4202B. doi:10.1103/PhysRevB.82.224202.
- ^ Skinner, L.B.; et al. (2012). "Structure of Molten CaSiO3: Neutron Diffraction Isotope Substitution with Aerodynamic Levitation and Molecular Dynamics Study". J. Phys. Chem. B. 116 (45): 13439–13447. doi:10.1021/jp3066019.
- ^ Eckersley, M.C.; et al. (1988). "Structural ordering in a calcium silicate glass". Nature. 355: 525–527. Bibcode:1988Natur.335..525E. doi:10.1038/335525a0.
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