Minerals chalcedony

Silica concentration in deep ground water in the granitic rock area (e.g., Kamaishi, Japan) is in equilibrium with SiOz mineral (chalcedony) (Fig. 1.27). Based on a coupled fluid flow-dissolution-precipitation kinetics model the relationship between residence time of deep ground water and A/M was derived, and the reasonable values of x is estimated to be more than 40 years (Shikazono and Fujimoto 2001). 

Many natural waters are supersaturated at low temperature, primarily because less stable minerals dissolve more quickly than more stable minerals precipitate. Relatively unstable silica phases such as chalcedony or amorphous silica, for example, may control a fluid s SiC>2 concentration because quartz, the most stable silica mineral, precipitates slowly. 

Several chemical geothermometers are in widespread use. The silica geothermometer (Fournier and Rowe, 1966) works because the solubilities of the various silica minerals (e.g., quartz and chalcedony, Si02) increase monotonically with temperature. The concentration of dissolved silica, therefore, defines a unique equilibrium temperature for each silica mineral. The Na-K (White, 1970) and Na-K-Ca (Fournier and Truesdell, 1973) geothermometers take advantage of the fact that the equilibrium points of cation exchange reactions among various minerals (principally, the feldspars) vary with temperature. 

From a plot of the saturation states of the silica polymorphs (Fig. 23.7), the fluid s equilibrium temperature with quartz is about 100 °C. Quartz, however, is commonly supersaturated in geothermal waters below about 150 °C and so can give erroneously high equilibrium temperatures when applied in geothermometry (Fournier, 1977). Chalcedony is in equilibrium with the fluid at about 76 °C, a temperature consistent with that suggested by the aluminosilicate minerals. 

Fig. 23.7. Calculated saturation indices (log Q/K) of silica minerals for Gjogur hot spring water. Chalcedony is approximately in equilibrium at 80 °C, but quartz is supersaturated at this temperature.

Si02 is one of the most abundant compounds in nature. It forms a number of minerals and several varieties whose names are quite familiar agate, car-nelian, sard, amethyst, chalcedony, flint, and chert. All are composed of Si02 with only small or trace amounts of other elements or compounds included during crystallization. In many cases it is the additional components that impart the peculiar color, optical, or physical properties to these minerals. The names are familiar because since ancient times these minerals were used or commonly set in jewelry. All of the names are varieties of the mineral quartz, the stable form of SiOj, formed at ordinary temperatures and pressures. Si02 also forms several polymorphs, which are mentioned below. 

The optical character of chalcedony is distinct from that expected for the normally uniaxial mineral, quartz, and signals the fibrous nature of a particular sample. The direction of fiber elongation is often parallel to the [1120] crystallographic direction of the quartz structure (Fig. 2.19A), but other fiber directions have also been determined within a single sample (Frondel, 1985). The presence of helically twisted fibers are suspected from the variations in extinction and birefringence noted along the fiber length (Fig. 2.19C). More detailed information on the optical or other physical and chemical properties of quartz and its many varieties can be found in volume 3 of Palache et al. (1962) and in Frondel (1985). 

The spectra of the green laser-induced luminescence represented in Fig. 4.4a, together with their decay time, also allows its association with These luminescence spectra strongly differ from the spectral parameters of all known uranyl minerals. For this reason it is not possible to connect this type of green luminescence with finely dissipated uranyl phases. On the other hand, this luminescence is very similar in such different host minerals as sedimentary apatites, opalites, chalcedony, chert, quartz and barites. Luminescence independence from the minerals structure evidences that it may be connected with uranyl adsorption on the minerals surface, supposedly in the form of (UO2 X nH20)2+. 

Most commonly, zeolites are found in series of sedimentary rocks which contain pyroclastic material and are formed during the devitrification of this material. If the rocks are silica-rich, the zeolite species formed seems dependent upon the bulk composition and burial depth or temperature of formation (Hay, 1966). They are most frequently accompanied by silica in an amorphous or cryptocrystalline form (opal, chalcedony). Analcite and all other compositional intermediates up to the silica-rich clinoptilolite are found in this association. The most comifton clay mineral in such tuffs is montmorillonite. Zeolites are sometimes found with glauconite (Brown, et al . 1969) or celadonite (Hay, 1966 Iijima, 1970 Read and Eisenbacher, 1974) in pelitic layers or acidic eruptive rocks... 

Next to materials of the glass-ceramics type, many varieties of chalcedony, such as agate, carneol, onyx, sardonyx, heliotrope and jasper, exhibit similar changes in hardness resulting from different consolidation of the cryptocrystalline structure of silica among mineral individuals. 

CARNEL1AN. The mineral camelian is a red or reddish-brown chalcedony the word is derived from the Latin word meaning flesh, in reference to the flesh color sometimes exhibited. See also Chalcedony. 

Fossils that have been replaced with minerals are called pseudomorphs. This word means false form, referring to the specimen that has the form of one thing, but the composition of something else. Most fossil pseudomorphs are made of chalcedony (microcrystalline quartz). 

The minerals found in United States coals continue to be studied with the availability of improved instrumental procedures such as x-ray diffraction, infrared absorption, and scanning electron microscopy beyond the traditional optical and chemical mineralogical techniques as applied to thin sections, polished pellets, and isolated particles. The minerals may be grouped into the silicates (kaolinite, illite montmorillonite, and chlorite), the oxides (quartz, chalcedony, hematite) the sulfides (pyrite, marcasite, and sphalerite) the sulfates (jarosite, gypsum, barite, and numerous iron sulfate minerals) the carbonates (ankerite, calcite, dolomite, and siderite) and numerous accessory minerals (apatite, phosphorite, zircon, rutile, chlorides, nitrates, and trace minerals). 

The proof of reversibility in primary mineral weathering would be instances where primary mineral structures have formed under earth-surface conditions. There are reports that secondary quartz can slowly precipitate at room temperature from solutions supersaturated with monosilicic acid. More typically, however, precipitated silica in soils is structurally disordered, in the form of chalcedony or opal. In fact, as long as alumina is present, silica does not precipitate as a separate phase, reacting instead to form aluminosilicates (layer silicates, imogolite, or allophane). 

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