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Natural Gypsum

Gonfiantiiii R, Fontes JC (1963) Oxygen isotopic fractionation in the water of crystallization of gypsum. Nature 200 644-646... [Pg.54]

Gypsum. Natural hydrated calcium sulphate, CaS04. 2H2O, from which PLASTER of PARIS (q.v.) is produced. In England gypsum occurs in the Newark and Tutbury zones of the Keuper Marl, and in the Purbeck Beds of Sussex. It occurs abundantly in USA, Canada, France, USSR and elsewhere. [Pg.148]

Sulfur occurs native in the vicinity of volcanos and hot springs. It is widely distributed in nature as iron pyrites, galena, sphalerite, cinnabar, stibnite, gypsum, epsom salts, celestite, barite, etc. [Pg.38]

Calcium is a metallic element, fifth in abundance in the earth s crust, of which if forms more than 3%. It is an essential constituent of leaves, bones, teeth, and shells. Never found in nature uncombined, it occurs abundantly as limestone, gypsum, and fluorite. Apatite is the fluorophosphate or chlorophosphate of calcium. [Pg.47]

Some commonly used primary nutrient fertilizers are incidentally also rich sources of calcium. Ordinary superphosphate contains monocalcium phosphate and gypsum in amounts equivalent to all of the calcium originally present in the phosphate rock. Triple superphosphate contains soluble monocalcium phosphate equivalent to essentially all the P2 5 product. Other fertilizers rich in calcium are calcium nitrate [10124-37-5] calcium ammonium nitrate [39368-85-9] and calcium cyanamide [156-62-7]. The popular ammonium phosphate-based fertilizers are essentially devoid of calcium, but, in view of the natural calcium content of soils, this does not appear to be a problem. [Pg.242]

World resources of sulfur have been summarized (110,111). Sources, ie, elemental deposits, natural gas, petroleum, pyrites, and nonferrous sulfides are expected to last only to the end of the twenty-first century at the world consumption rate of 55.6 x 10 t/yr of the 1990s. However, vast additional resources of sulfur, in the form of gypsum, could provide much further extension but would require high energy consumption for processing. [Pg.245]

Calcium. Calcium is the fifth most abundant element in the earth s cmst. There is no foreseeable lack of this resource as it is virtually unlimited. Primary sources of calcium are lime materials and gypsum, generally classified as soil amendments (see Calcium compounds). Among the more important calcium amendments are blast furnace slag, calcitic limestone, gypsum, hydrated lime, and precipitated lime. Fertilizers that carry calcium are calcium cyanamide, calcium nitrate, phosphate rock, and superphosphates. In addition, there are several organic carriers of calcium. Calcium is widely distributed in nature as calcium carbonate, chalk, marble, gypsum, fluorspar, phosphate rock, and other rocks and minerals. [Pg.245]

The calcium sulfate [7778-18-9] discharged from the furnace can also be recovered. This is less the practice in the United States where natural gypsum is plentiful and inexpensive than in Europe, where CaSO recovery for use in cement (qv) and self-leveling floors is common. Some CaSO is recovered in the United States, primarily for lower end uses such as road aggregate. [Pg.196]

Soil conditioners are materials that measurably improve the physical characteristics of the soil as a plant growth medium. Typical uses include erosion control, prevention of surface sealing, and improvement of water infiltration and drainage. Many natural materials such as peat and gypsum are used alone or in combination with synthetics for soil conditioning. This article is concerned with synthetic soil conditioners, many of which are introduced as polymeric systems similar to the gels and foams formed in situ by chemical grouts. [Pg.227]

Sulfur constitutes about 0.052 wt % of the earth s cmst. The forms in which it is ordinarily found include elemental or native sulfur in unconsohdated volcanic rocks, in anhydrite over salt-dome stmctures, and in bedded anhydrite or gypsum evaporate basin formations combined sulfur in metal sulfide ores and mineral sulfates hydrogen sulfide in natural gas organic sulfur compounds in petroleum and tar sands and a combination of both pyritic and organic sulfur compounds in coal (qv). [Pg.115]

Neither of these processes has been commercialized, although some aspects of the methodology were incorporated into a plant operated for a short time by the Elcor Company (31). This company, which operated briefly in western Texas in 1968 using natural gypsum, is the only one known to have commercially attempted to recover elemental sulfur from this material by a two-step thermal process. The Elcor plant was shut down shortly after it began operation. Although most technical problems were said to have been solved, production costs were prohibitive. [Pg.120]

Gypsum [13397-24-5] CaSO 2H20, is a naturally occurring mineral found mainly in the western United States and eastern Canada (see Calcium COMPOUNDS, CALCIUM sulfate). The purer deposits require only minimal beneficiation to get a product pure enough for commercial appHcations. Other... [Pg.321]

Calcium sulfate [7778-18-9J, CaSO, ia mineral form is commonly called gypsum and occurs abundandy ia many areas of the wodd. In natural deposits, the main form is the dihydrate. Some anhydrite is also present ia most areas, although to a lesser extent. Mineral composition can be found ia Table 1. [Pg.418]

The natural ore is quarried or mined ia many areas of North America and Europe. Treading North American regions iaclude Canada, Mexico, and ia the United States, California, Texas, Nevada, Iowa, Kansas, Ohio, Indiana, and Michigan. In Europe, Erance, Spain, Italy, the United Kingdom, and Russia have significant deposits of natural gypsum, as does Germany. [Pg.418]

Anhydrite also has several common classifications. Anhydrite I designates the natural rock form. Anhydrite 11 identifies a relatively insoluble form of CaSO prepared by high temperature thermal decomposition of the dihydrate. It has an orthorhombic lattice. Anhydrite 111, a relatively soluble form made by lower temperature decomposition of dihydrate, is quite unstable converting to hemihydrate easily upon exposure to water or free moisture, and has the same crystal lattice as the hemihydrate phase. Soluble anhydrite is readily made from gypsum by dehydration at temperatures of 140—200°C. Insoluble anhydrite can be made by beating the dihydrate, hemihydrate, or soluble anhydrite for about 1 h at 900°C. Conversion can also be achieved at lower temperatures however, longer times are necessary. [Pg.419]

Gypsum is widely distributed naturally as calcium sulfate dihydrate [101012-1-4], CaS04-2H2 0. When partially calcined, the hemihydrate, CaS04 H2 0, is formed (see Calciumcompounds-calciumsulfates). Gypsum has been used in one form since 1756 for making dental casts, and in another form since 1844 for dental impressions (101). [Pg.475]

X-ray evidence shows the material to be completely amorphous as might be expected from such a complex mixture. The specific gravity ranges from 1.05 to 1.10. It is slightly harder than gypsum and therefore just not possible to scratch with a fingernail. Yellow in colour, it is less brittle than other hard natural resins and may therefore be carved or machined with little difficulty. The refractive index is 1.54. [Pg.871]

Traditionally ceramic raw materials have been dug out of the ground and used with little or no treatment or purification. Sand, fireclay, talc, and gypsum are examples. The energy expenditure for producing these materials is therefore small. Some of these materials can be found naturally in high purity. Silica sands (SiO,) with less than 100 ppm (parts per mil-... [Pg.773]

The amount of hardness present in natural surface and groundwaters depends to a large extent on the action of dissolved carbon dioxide in rainwater on the watershed s geological formations (such as limestone, dolomite, gypsum, or magnesite). The dissolved hardness levels remain relatively low because of the sparingly soluble nature of the salts formed. Typically, MU water sources initially contain anywhere from 5... [Pg.221]

The equilibrium constant is small, indicating a slightly soluble salt, as we would expect for a naturally occurring mineral like gypsum. [Pg.1311]


See other pages where Natural Gypsum is mentioned: [Pg.71]    [Pg.785]    [Pg.71]    [Pg.785]    [Pg.75]    [Pg.76]    [Pg.378]    [Pg.406]    [Pg.212]    [Pg.420]    [Pg.425]    [Pg.229]    [Pg.115]    [Pg.120]    [Pg.123]    [Pg.201]    [Pg.406]    [Pg.418]    [Pg.418]    [Pg.418]    [Pg.418]    [Pg.419]    [Pg.419]    [Pg.421]    [Pg.293]    [Pg.470]    [Pg.477]    [Pg.507]    [Pg.1862]    [Pg.108]    [Pg.651]    [Pg.12]    [Pg.494]   
See also in sourсe #XX -- [ Pg.418 ]




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Gypsum

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