Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Carbonates aragonite

The carbonate minerals that comprise limestone ate calcite [13397-26-7] (calcium carbonate), which is easily the most abundant mineral type aragonite [14791-73-2] (calcium carbonate) dolomite [17069-72-6] (double carbonate of calcium and magnesium) andmagnesite [13717-31 -5] (magnesium carbonate). Individual limstone types ate further described by many common names (1). Some of this nomenclature is repetitious and overlapping. The following terms ate in common use in Europe and the United States. [Pg.163]

A significant advantage of the PLM is in the differentiation and recognition of various forms of the same chemical substance polymorphic forms, eg, brookite, mtile, and anatase, three forms of titanium dioxide calcite, aragonite and vaterite, all forms of calcium carbonate Eorms I, II, III, and IV of HMX (a high explosive), etc. This is an important appHcation because most elements and compounds possess different crystal forms with very different physical properties. PLM is the only instmment mandated by the U.S. Environmental Protection Agency (EPA) for the detection and identification of the six forms of asbestos (qv) and other fibers in bulk samples. [Pg.333]

Aragonite. Calcium carbonate is a common deposit in shallow tropical waters as a constituent of muds, or in the upper part of coral reefs where it precipitates from carbon dioxide-rich waters supersaturated with carbonate from intense biological photosynthesis and solar heating. Deposits of ooHtic aragonite, CaCO, extending over 250,000 km in water less than 5 m deep ate mined for industrial purposes in the Bahamas for export to the United States (19). [Pg.285]

Strontium Carbonate. Strontium carbonate, SrCO, occurs naturally as strontianite in orthorhombic crystals and as isomorphs with aragonite, CaCO, and witherite, BaCO. There are deposits in the United States in Schoharie County, New York in WestphaUa, Germany and smaller deposits in many other areas. None is economically workable. Strontianite has a specific gravity of 3.7, a Mohs hardness of 3.5, and it is colorless, gray, or reddish in color. [Pg.474]

The choice of selected raw materials is very wide, but they must provide calcium oxide (lime), iron oxide [1309-37-1/, siHca, and aluminum oxide (alumina). Examples of the calcereous (calcium oxide) sources are calcium carbonate minerals (aragonite [14791-73-2] calcite [13397-26-7] limestone [1317-65-3] or mad), seasheUs, or shale. Examples of argillaceous (siHca and alumina) sources are clays, fly ash, mad, shale, and sand. The iron oxide commonly comes from iron ore, clays, or mill scale. Some raw matedals supply more than one ingredient, and the mixture of raw matedals is a function of their chemical composition, as deterrnined by cost and availabiHty. [Pg.322]

The commercial grades of calcium carbonate from natural sources are either calcite, aragonite, or sedimentary chalk. In most precipitated grades aragonite is the predominant crystal stmcture. The essential properties of the two common crystal stmctures are shown in Table 1. [Pg.410]

A wide variety of precipitates form in cooling water systems carbonates, silicates, sulfates, and phosphates are common. Below and slightly above 212°F (100°C), calcite, aragonite, gypsum, hydroxyapatite, magnesium phosphate, anhydrite, and serpentine are commonly encountered (see Table 4.1). [Pg.73]

Of course, freezing of a liquid - or its inverse - are themselves phase transformations, but the scientific study of freezing and melting was not developed until well into the 20th century (Section 9.1.1). Polymorphism also links with metastability thus aragonite, one polymorphic form of calcium carbonate, is under most circumstances metastable to the more familiar form, calcite. [Pg.99]

An increase in carbonate-ion concentration moves the equilibrium in favour of calcium carbonate deposition. Thus one secondary effect of cathodic protection in seawater is the production of OH , which favours the production of CO, , which in turn promotes the deposition of CaCOj. Cathodically protected surfaces in seawater will often develop an aragonite (CaCOj) film. This film is commonly referred to as a calcareous deposit. [Pg.129]

In areas of the system where the heat gradient is less severe, calcium carbonate precipitates in both crystalline and amorphous forms. It may precipitate as a calcite or aragonite sludge, but more usually an aragonite scale is produced. Aragonite is hard and adherent, depositing in FW lines and various boiler surface components such as boiler tubes. [Pg.224]

Calcium carbonate Aragonite CaC03 Low temperature scale. [Pg.267]

Oceanic surface water is everywhere supersaturated with respect to the two solid calcium carbonate species calcite and aragonite. Nevertheless carbonate precipitation is exclusively controlled by biological processes, specifically... [Pg.290]

The detrital rain of carbon-containing particles can be divided into two groups the hard parts comprising calcite and aragonite and the soft tissue containing organic carbon. The composition of the soft tissue shows surprising... [Pg.291]

The solubility of calcite and aragonite increases with increasing pressure and decreasing temperature in such a way that deep waters are undersaturated with respect to calcium carbonate, while surface waters are supersaturated. The level at which the effects of dissolution are first seen on carbonate shells in the sediments is termed the lysocline and coincides fairly well with the depth of the carbonate saturation horizon. The lysocline commonly lies between 3 and 4 km depth in today s oceans. Below the lysocline is the level where no carbonate remains in the sediment this level is termed the carbonate compensation depth. [Pg.292]

Grossman, E. and Ku, T.-L. 1986 Oxygen and carbon isotope fractionation in biogenic aragonite temperature effects. Chemical Geology (Isotope Geoscience Section) 59 59-74. [Pg.209]

The equations governing the age of secondary carbonate deposits stated above assume that all °Th or Pa present in the mineral is formed in situ by radioactive decay of co-precipitated U. Thorium and Pa content at time of formation can often be considered to be negligible in the pure authigenic phase of calcite or aragonite... [Pg.412]


See other pages where Carbonates aragonite is mentioned: [Pg.363]    [Pg.386]    [Pg.3194]    [Pg.153]    [Pg.473]    [Pg.363]    [Pg.386]    [Pg.3194]    [Pg.153]    [Pg.473]    [Pg.40]    [Pg.75]    [Pg.233]    [Pg.273]    [Pg.835]    [Pg.285]    [Pg.410]    [Pg.55]    [Pg.61]    [Pg.120]    [Pg.122]    [Pg.645]    [Pg.716]    [Pg.297]    [Pg.297]    [Pg.199]    [Pg.143]    [Pg.143]    [Pg.367]    [Pg.378]    [Pg.396]    [Pg.397]    [Pg.398]    [Pg.399]    [Pg.416]    [Pg.439]    [Pg.82]    [Pg.405]    [Pg.410]    [Pg.484]   
See also in sourсe #XX -- [ Pg.60 ]




SEARCH



Aragonite

Aragonite carbon enrichment

Aragonite carbonate compensation depth

Calcium carbonate Aragonite

Calcium carbonate Aragonite, Calcite

Calcium carbonate acicular aragonite

Calcium carbonate, analysis aragonite

Calcium carbonates , fillers aragonite

Carbonate minerals aragonite solubility

© 2024 chempedia.info