Nontronite

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Nontronite
Mineraly.sk - nontronit.jpg
Nontronite from Slovakia
General
Category Phyllosilicates
Smectite group
Formula
(repeating unit)
(CaO0.5,Na)0.3Fe3+2(Si,Al)4O10(OH)2·nH2O
IMA symbol Non [1]
Strunz classification 9.EC.40
Crystal system Monoclinic
Space group C2/m (no. 12)
Identification
ColorYellow, olive-green, green, orange, brown
Crystal habit Earthy masses
Cleavage Perfect basal
Fracture uneven
Mohs scale hardness1.5 to 2
Luster Earthy to dull
Streak Colorless
Specific gravity 2.3
Optical propertiesBiaxial (−)
Refractive index nα = 1.530–1.580; nβ = 1.555–1.612; nγ = 1.560–1.615
Birefringence δ = 0.030–0.035
References [2] [3] [4] [5]

Nontronite is the iron(III) rich member of the smectite group of clay minerals. Nontronites typically have a chemical composition consisting of more than ~30% Fe 2 O 3 and less than ~12% Al 2O3 (ignited basis). Nontronite has very few economic deposits like montmorillonite. [6] [7] Like montmorillonite, nontronite can have variable amounts of adsorbed water associated with the interlayer surfaces and the exchange cations.

A typical structural formula for nontronite is Ca .5(Si 7Al.8Fe.2)(Fe3.5Al.4 Mg .1)O20(OH)4. [8] The dioctahedral sheet of nontronite is composed mainly of trivalent iron (Fe3+) cations, although some substitution by trivalent aluminium (Al3+) and divalent magnesium (Mg2+) does occur. The tetrahedral sheet is composed mainly of silicon (Si4+), but can have substantial (about 1 in 8) substitution of either Fe3+ or Al3+, or combinations of these two cations. Thus, nontronite typically is characterised by having most (usually greater than 60%) of the layer charge located in the tetrahedral sheet. The layer charge is typically balanced by divalent calcium (Ca2+) or magnesium (Mg2+).

Nontronite forms from the weathering of biotite and basalts, precipitation of iron and silicon rich hydrothermal fluids and in deep sea hydrothermal vents. [9] [10] Some evidence suggests that microorganisms may play an important role in their formation. [11] Microorganisms are also involved in reduction of structural iron in nontronite when soils undergo anoxia, and the reduced form of the clay appears to be highly reactive towards certain pollutants, perhaps contributing to the destruction of these compounds in the environment. [12] [13]

The only known commercially viable and operational nontronite mine is located in Canterbury, New Zealand. The mine is operated by Palmer Resources and the finished products are used internationally in industrial applications (pulp & paper, surface coating) and in cosmetics marketed as New Zealand Glacial Clay. [14]

See also

Related Research Articles

<span class="mw-page-title-main">Bentonite</span> Rock type or absorbent swelling clay

Bentonite is an absorbent swelling clay consisting mostly of montmorillonite which can either be Na-montmorillonite or Ca-montmorillonite. Na-montmorillonite has a considerably greater swelling capacity than Ca-montmorillonite.

<span class="mw-page-title-main">Jarosite</span> Alunite supergroup, potassium iron basic sulfate mineral

Jarosite is a basic hydrous sulfate of potassium and ferric iron (Fe-III) with a chemical formula of KFe3(SO4)2(OH)6. This sulfate mineral is formed in ore deposits by the oxidation of iron sulfides. Jarosite is often produced as a byproduct during the purification and refining of zinc and is also commonly associated with acid mine drainage and acid sulfate soil environments.

<span class="mw-page-title-main">Vivianite</span> Phosphate mineral

Vivianite (Fe2+
3
(PO
4
)
2
·8H
2
O
) is a hydrated iron phosphate mineral found in a number of geological environments. Small amounts of manganese Mn2+, magnesium Mg2+, and calcium Ca2+ may substitute for iron Fe2+ in the structure. Pure vivianite is colorless, but the mineral oxidizes very easily, changing the color, and it is usually found as deep blue to deep bluish green prismatic to flattened crystals.
Vivianite crystals are often found inside fossil shells, such as those of bivalves and gastropods, or attached to fossil bone.

<span class="mw-page-title-main">Clay mineral</span> Fine-grained aluminium phyllosilicates

Clay minerals are hydrous aluminium phyllosilicates (e.g. kaolin, Al2Si2O5(OH)4), sometimes with variable amounts of iron, magnesium, alkali metals, alkaline earths, and other cations found on or near some planetary surfaces.

<span class="mw-page-title-main">Montmorillonite</span> Phyllosilicate group of minerals

Montmorillonite is a very soft phyllosilicate group of minerals that form when they precipitate from water solution as microscopic crystals, known as clay. It is named after Montmorillon in France. Montmorillonite, a member of the smectite group, is a 2:1 clay, meaning that it has two tetrahedral sheets of silica sandwiching a central octahedral sheet of alumina. The particles are plate-shaped with an average diameter around 1 μm and a thickness of 0.96 nm; magnification of about 25,000 times, using an electron microscope, is required to resolve individual clay particles. Members of this group include saponite, nontronite, beidellite, and hectorite.

<span class="mw-page-title-main">Illite</span> Group of non-expanding clay minerals

Illite, also called hydromica or hydromuscovite, is a group of closely related non-expanding clay minerals. Illite is a secondary mineral precipitate, and an example of a phyllosilicate, or layered alumino-silicate. Its structure is a 2:1 sandwich of silica tetrahedron (T) – alumina octahedron (O) – silica tetrahedron (T) layers. The space between this T-O-T sequence of layers is occupied by poorly hydrated potassium cations which are responsible for the absence of swelling. Structurally, illite is quite similar to muscovite with slightly more silicon, magnesium, iron, and water and slightly less tetrahedral aluminium and interlayer potassium. The chemical formula is given as (K,H3O)(Al,Mg,Fe)2(Si,Al)4O10[(OH)2·(H2O)], but there is considerable ion (isomorphic) substitution. It occurs as aggregates of small monoclinic grey to white crystals. Due to the small size, positive identification usually requires x-ray diffraction or SEM-EDS analysis. Illite occurs as an altered product of muscovite and feldspar in weathering and hydrothermal environments; it may be a component of sericite. It is common in sediments, soils, and argillaceous sedimentary rocks as well as in some low grade metamorphic rocks. The iron-rich member of the illite group, glauconite, in sediments can be differentiated by x-ray analysis.

<span class="mw-page-title-main">Smectite</span> Mineral mixture of phyllosilicates

A smectite is a mineral mixture of various swelling sheet silicates (phyllosilicates), which have a three-layer 2:1 (TOT) structure and belong to the clay minerals. Smectites mainly consist of montmorillonite, but can often contain secondary minerals such as quartz and calcite.

<span class="mw-page-title-main">Celadonite</span>

Celadonite is a mica group mineral, a phyllosilicate of potassium, iron in both oxidation states, aluminium and hydroxide with formula K(Mg,Fe2+
)(Fe3+
,Al)[Si
4
O
10
](OH)
2
.

<span class="mw-page-title-main">Ceylonite</span>

Ceylonite and pleonaste or pleonast are dingy blue or grey to black varieties of spinel. Ceylonite, named for the island of Ceylon, is a ferroan spinel with Mg:Fe from 3:1 and 1:1, and little or no ferric iron. Pleonaste is named from the Greek for 'abundant,' for its many crystal forms, and is distinguished chemically by low Mg:Fe ratios of approximately 1:3. It is sometimes used as a gemstone.

<span class="mw-page-title-main">Galaxite</span>

Galaxite, also known as 'mangan-spinel' is an isometric mineral belonging to the spinel group of oxides with the ideal chemical formula Mn2+Al2O4.

<span class="mw-page-title-main">Greigite</span> Iron sulfide mineral of spinel structure

Greigite is an iron sulfide mineral with the chemical formula Fe2+Fe3+2S4. It is the sulfur equivalent of the iron oxide magnetite (Fe3O4). It was first described in 1964 for an occurrence in San Bernardino County, California, and named after the mineralogist and physical chemist Joseph W. Greig (1895–1977).

An AFm phase is an "alumina, ferric oxide, monosubstituted" phase, or aluminate ferrite monosubstituted, or Al2O3, Fe2O3 mono, in cement chemist notation (CCN). AFm phases are important hydration products in the hydration of Portland cements and hydraulic cements.

<span class="mw-page-title-main">Layered double hydroxides</span> Class of ionic solids characterized by a layered structure

Layered double hydroxides (LDH) are a class of ionic solids characterized by a layered structure with the generic layer sequence [AcB Z AcB]n, where c represents layers of metal cations, A and B are layers of hydroxide anions, and Z are layers of other anions and neutral molecules. Lateral offsets between the layers may result in longer repeating periods.

<span class="mw-page-title-main">Mawrth Vallis</span> Valley on Mars

Mawrth Vallis is a valley on Mars, located in the Oxia Palus quadrangle at 22.3°N, 343.5°E with an elevation approximately two kilometers below datum. Situated between the southern highlands and northern lowlands, the valley is a channel formed by massive flooding which occurred in Mars’ ancient past. It is an ancient water outflow channel with light-colored clay-rich rocks.

<span class="mw-page-title-main">Gedrite</span>

Gedrite is a crystal belonging to the orthorhombic ferromagnesian subgroup of the amphibole supergroup of the double chain inosilicate minerals with the ideal chemical formula Mg2(Mg3Al2)(Si6Al2)O22(OH)2.

<span class="mw-page-title-main">Chamosite</span> Phyllosilicate mineral member of the chlorite group

Chamosite is the Fe2+end member of the chlorite group. A hydrous aluminium silicate of iron, which is produced in an environment of low to moderate grade of metamorphosed iron deposits, as gray or black crystals in oolitic iron ore. Like other chlorites, it is a product of the hydrothermal alteration of pyroxenes, amphiboles and biotite in igneous rock. The composition of chlorite is often related to that of the original igneous mineral so that more Fe-rich chlorites are commonly found as replacements of the Fe-rich ferromagnesian minerals (Deer et al., 1992).

<span class="mw-page-title-main">Pimelite</span> Nickel-rich smectite deprecated as mineral species in 2006

Pimelite was discredited as a mineral species by the International Mineralogical Association (IMA) in 2006, in an article which suggests that "pimelite" specimens are probably willemseite, or kerolite. This was a mass discreditation, and not based on any re-examination of the type material. Nevertheless, a considerable number of papers have been written, verifying that pimelite is a nickel-dominant smectite. It is always possible to redefine a mineral wrongly discredited.

In geology and mineralogy, a mineral group is a set of mineral species with essentially the same crystal structure and composed of chemically similar elements.

<span class="mw-page-title-main">Coupled substitution</span> Geological process by which two elements simultaneously substitute into a crystal

Coupled substitution is the geological process by which two elements simultaneous substitute into a crystal in order to maintain overall electrical neutrality and keep the charge constant. In forming a solid solution series, ionic size is more important than ionic charge, as this can be compensated for elsewhere in the structure.

The soil matrix is the solid phase of soils, and comprise the solid particles that make up soils. Soil particles can be classified by their chemical composition (mineralogy) as well as their size. The particle size distribution of a soil, its texture, determines many of the properties of that soil, in particular hydraulic conductivity and water potential, but the mineralogy of those particles can strongly modify those properties. The mineralogy of the finest soil particles, clay, is especially important.

References

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  2. Anthony, John W.; Bideaux, Richard A.; Bladh, Kenneth W.; Nichols, Monte C. (2005). "Nontronite" (PDF). Handbook of Mineralogy. Mineral Data Publishing. Retrieved 28 July 2022.
  3. Barthelmy, David (2014). "Nontronite Mineral Data". Webmineral.com. Retrieved 28 July 2022.
  4. Nontronite, Mindat.org , retrieved 28 July 2022
  5. Dainyak, Lidia G.; Zviagina, Bella B.; Rusakov, Viacheslav S.; Drits, Victor A. (2006). "Interpretation of the nontronite-dehydroxylate Mossbauer spectrum using EFG calculations". European Journal of Mineralogy. 18 (6): 753–764. Bibcode:2006EJMin..18..753D. doi:10.1127/0935-1221/2006/0018-0753.
  6. Eggleton, R. A. (1977), Clay minerals, vol. 12, pp. 181–194
  7. Keeling; et al. (2000). "Geology and Characterization of Two Hydrothermal Nontronites from Weathered Metamorphic Rocks at the Uley Graphite Mine, South Australia". Clays and Clay Minerals. 48 (5): 537–548. Bibcode:2000CCM....48..537K. doi:10.1346/CCMN.2000.0480506. S2CID   129598259.
  8. Gates; et al. (2002). "Mountainville nontronite". Clays and Clay Minerals. 50: 223–239. doi:10.1346/000986002760832829. S2CID   95954306.
  9. Bischoff (1972), Clays and Clay Minerals, vol. 20, pp. 217–223
  10. Eggleton, R. A. (1975). "Nontronite topotaxial after hedenbergite". American Mineralogist. 60: 1063–1068.
  11. Kohler; et al. (1994), Clays and Clay Minerals, vol. 42, pp. 680–701
  12. Tor, J., C. Xu, J. M. Stucki, M. Wander, G. K. Sims (2000). "Trifluralin degradation under micro-biologically induced nitrate and Fe(III) reducing conditions". Env. Sci. Tech. 34: 3148–3152.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  13. Xu, J., J. W. Stucki, J. Wu, J. Kostka, and G. K. Sims (2001). "Fate of atrazine and alachlor in redox-treated ferruginous smectite". Env. Tox. & Chem. 20: 2717–2724.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  14. "New Zealand Glacial Clay Fact Sheet". Palmer Resources Limited.