A reddish-brown phosphate mineral containing rare-earth metals, (Ce, La, Y, Th)PO4, important as a source of cerium and thorium.
[Greek monazein, to live alone; see monastery + -ITE1.]
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mon·a·zite (mŏn'ə-zīt') ![]() |
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A rare mineral that incorporates the light rare-earth elements (lanthanum, cerium, praseodymium, neodymium, promethium, samarium, europium, gadolinium) and also yttrium. Monazite has a general formula of (La,Ce, Nd)PO4, but Pr, Sm, Eu, Gd, and Y substitute for La, Ce, and Nd in solid solution in minor amounts. The dominant rare-earth element in a particular monazite is denoted by the atomic suffix, such as monazite-(Ce) in which cerium exists in amounts greater than other rare-earth atoms. Monazite-(Ce), monazite-(La), and monazite-(Nd) are officially recognized by the International Mineralogical Association. See also Cerium; Mineral; Rare-earth elements; Yttrium.
The atomic arrangement of monazite is formed of a packing arrangement of (PO4) tetrahedra and distorted (REO9) polyhedra, where RE = the rare-earth elements in the particular monazite mineral. The arrangement is formed of chains of alternating phosphate tetrahedra and RE polyhedra, parallel to the c axis. Monazite is similar in structure and chemistry to the tetragonal mineral xenotime, Y(PO4), that selectively incorporates the heavy rare-earth elements. See also Phosphate minerals.
Monazite is variably green, yellow, brown, or red-brown, and rarely occursin crystals large enough to discern with the unaided eye. Mohs hardness is5–5.5, and the specific gravity is 4.6–5.5, varying withsubstitution of different elements.
Monazite is one of the main ore minerals for the rare-earth elements thatare used in the manufacture of television and computer screens, fluorescentlight bulbs, and highly efficient batteries, among other industrialapplications.
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Environment
Pegmatites, specks in plutonic rocks, and concentrated in heavy-sand placers.
Crystal descriptionUsually in small, red-brown, embedded, opaque, flattened crystals whose skewed monoclinic symmetry is obvious. Also found in sand, in light yellow-brown, transparent, rolled grains.
Physical propertiesYellow to reddish brown. Luster subadamantine to resinous; hardness 5-5Ɖ; specific gravity 4.9-5.3; streak light yellow-brown; fracture conchoidal to uneven; cleavage 1 good, several poor, with well-developed basal parting (especially in stressed embedded crystals). Brittle; transparent to translucent; strong absorption lines in the spectrum (use spectroscope).
CompositionPhosphate of cerium, lanthanum--usually with some yttrium, a little uranium, and considerable amounts of thorium and silica (about 35% Ce 2 O 3 , 35% La 2 O 3 , and 30% P 2 O 5 ).
TestsOn charcoal infusible, but turns gray. After fired grain is moistened with sulfuric acid and reheated, a bluish green flash (phosphorous) can be seen around the assay.
Distinguishing characteristicsThis is a potential future gem, when a locality is found. In color and occurrence, monazite resembles some zircons and some sphenes but is not fluorescent, and the crystal shape is very different. The oblique cleavages and parting make it break into splinters (red-brown fragments) that are rather characteristic. Difficult to identify in sand (use a spectroscope).
OccurrenceMonazite forms small primary grains that are disseminated through many gneisses and granites. Since it is heavy and more resistant to weathering than the rock-making minerals, it frequently persists, along with quartz and other heavy grains, in beach or river sand. Deposits of monazite-rich sands are dug and separated for the recovery of several valuable minerals. The thorium oxide content is high enough to make the monazite valuable as an ore of that substance. Once in strong demand for the manufacture of Welsbach gaslight mantles, where it still has a small role. Commercial deposits of monazite occur in Travancore, India, in Brazil, and along the North Carolina and Florida coasts.
Monazite forms larger crystals in pegmatites, units that may be several inches (10 cm) across. Both Pomba and Divino de Uba, Minas Gerais, Brazil, and some pegmatites in northern Brazil are particularly rich in the mineral, associated with black euxenite, (with all the rare earth elements), polycrase, samarskite, and columbite (see samarskite, p. 173). Similar large brick red crystals are found in Norwegian biotite pegmatites, rich in rare earths, xenotime, fergusonite, and black mica. In the U.S. it has been found in pegmatites in Maine (Standpipe Hill), Connecticut (Norwich), Virginia (Amelia), Colorado (Boulder Co.), and New Mexico (Petaca district). Monazite sands are found from North Carolina to Florida, and in Idaho and California. Small greenish, changeable (alexandritic pinkish) crystals have been found in Llallagua, Bolivia tin mines.
Alpine crystal cavities sometimes contain small, clear, golden crystals perched on clear quartz, a type that was described under the name of turnerite. This type of monazite is widespread in France, Switzerland, and Austria.
| Wikipedia: Monazite |
| Monazite | |
| General | |
|---|---|
| Category | Phosphate mineral |
| Chemical formula | (Ce,La)PO4 |
| Identification | |
| Color | Reddish brown, brown, pale yellow, pink, gray |
| Crystal habit | Commonly as prismatic or wedge-shaped crystals |
| Crystal system | Monoclinic |
| Twinning | Contact twins common |
| Cleavage | Distinct on [100] poor on [010] |
| Fracture | Conchoidal to uneven |
| Mohs Scale hardness | 5.0 to 5.5 |
| Luster | Resinous, vitreous to adamantine |
| Diaphaneity | Translucent to opaque |
| Specific gravity | 4.6 - 5.7 (4.98–5.43 for Monazite-Ce) |
| Optical properties | Biaxial (+) 2V = 10 – 26° |
| Refractive index | α= 1.770–1.793 β = 1.778–1.800 γ = 1.823–1.860 |
| Pleochroism | Weak |
| Other characteristics | Radioactive if thorium-rich, dull brown cathodoluminescence, paramagnetic |
| References | [1] |
Monazite is a reddish-brown phosphate mineral containing rare earth metals and is an important source of thorium, lanthanum, and cerium. It occurs usually in small isolated crystals. There are actually at least four different kinds of monazite, depending on relative elemental composition of the mineral:
The elements in parentheses are listed in the order in which they are in relative proportion within the mineral, so that lanthanum is the most common rare earth in monazite-La, and so forth. Silica, SiO2, will be present in trace amounts, as will small amounts of uranium. Due to the alpha decay of thorium and uranium, monazite contains a significant amount of helium, which can be extracted by heating.
Monazite is an important ore for thorium, lanthanum, and cerium. It is often found in placer deposits. The deposits in India are particularly rich in monazite. It has a hardness of 5.0 - 5.5 and is relatively dense, about 4.6 to 5.7 g/cm3.
Because of the presence of thorium within monazite, it can be radioactive. If samples are kept, they should be placed away from minerals that can be damaged by radiation. Because of its radioactive nature, the monazite within rocks is a useful tool for dating geological events, such as heating or deformation of the rock.
The name monazite comes from the Greek μοναζειν (to be solitary), in allusion to its isolated crystals. India, Madagascar, and South Africa have large deposits of monazite sands.
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Monazite sand from Brazil was first noticed in sand carried in ship's ballast by Auer von Welsbach in the 1880s. Von Welsbach was looking for a way to obtain thorium for his newly invented incandescent mantles. Monazite sand was quickly adopted as the source of thorium for the mantles and was the foundation of what became the rare earth industry. Monazite sand was also briefly mined in North Carolina, but shortly thereafter the deposits in southern India were found. Brazilian and Indian monazite dominated the industry until the Second World War. Besides the deposits in Brazil and India there are also large deposits in Australia.
Monazite was the only significant source of commercial lanthanides until bastnaesite began to be processed in about 1965. With declining interest in thorium as a potential nuclear fuel in the 1960s and increased concern over the disposal of the radioactive daughter products of thorium, bastnaesite came to displace monazite in the production of lanthanides due to its much lower thorium content. However any future increase in interest in thorium for atomic energy will bring monazite back into commercial use.
Because of their high density monazite minerals will concentrate in alluvial sands when released by the weathering of pegmatites. These so-called placer deposits are often beach or fossil beach sands and contain other heavy minerals of commercial interest such as zircon and ilmenite. Monazite can be isolated as a nearly pure concentrate by the use of gravity, magnetic and electrostatic separation.
Monazite sand deposits are inevitably of the monazite-(Ce) composition. Typically the lanthanides in such monazites contain about 45 - 48 % cerium, about 24% lanthanum, about 17% neodymium, about 5% praseodymium, and minor quantities of samarium, gadolinium, and yttrium. Europium concentrations tend to be low, about 0.05%. South African "rock" monazite, from Steenkampskraal, was processed in the 1950s and early 1960s by the Lindsay Chemical Division of American Potash and Chemical Corporation, at the time the largest producer of lanthanides in the world. Steenkampskraal monazite provided a supply of the complete set of lanthanides. Very low concentrations of the heaviest lanthanides in monazite justified the term "rare" earth for these elements, with prices to match. Thorium content of monazite is variable and sometimes can be up to 20 - 30 %. Monazite from certain carbonatites, or from Bolivian tin veins is essentially thorium-free. However, commercial monazite sands typically contain between 6 and 12% thorium oxide.
The original process for "cracking" monazite so as to extract the thorium and lanthanide content was to heat it with concentrated sulfuric acid to temperatures between 120 and 150 °C for several hours. Variations in the ratio of acid to ore, the extent of heating, and the extent to which water was added afterwards led to several different processes to separate thorium from the lanthanides. One of the processes caused the thorium to precipitate out as a phosphate or pyrophosphate in crude form, leaving a solution of lanthanide sulfates from which the lanthanides could be easily precipitated as a double sodium sulfate. The acid methods led to the generation of considerable acid waste, and loss of the phosphate content of the ore.
A more recent process uses hot sodium hydroxide solution (73 %) at about 140 °C. This process allows the valuable phosphate content of the ore to be recovered as crystalline trisodium phosphate. The lanthanide/thorium hydroxide mixture can be treated with hydrochloric acid to provide a solution of lanthanide chlorides, and an insoluble sludge of the less-basic thorium hydroxide.
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