Big Chemical Encyclopedia

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

Articles Figures Tables About

Magnesium in nature

Metal complexes of phenols are important in nature and useful in the laboratory. The metals involved usually include iron, aluminum and magnesium. In nature the flavonoids account for most red, blue, and violet -and to some extent yellow - colors. The majority of yellow colors are the result of the presence of carotenoids and aurones. [Pg.43]

Atomic absorption spectroscopy The determination of magnesium in natural samples and cement by atomic absorption spectroscopy is reported [35]. The same technique is used for the analysis of leaf samples of varied origin and nature initially decomposed by fusion with sodium hydroxide in an open system using sodium nitrate as an auxiliary agent to facilitate the mineralization of most of the samples [36]. Another... [Pg.273]

A chemometric method for simultaneous determination of calcium and magnesium in natural waters using Arsenazo III and FIA system was described [5], The concentrations of the analytes were calculated by the H-point standard addition method for ternary mixtures. [Pg.491]

Sloan and Talbot [113] cathodically coupled 26-ply quasi-isotropic T300/ 934 carbon/epoxy laminate coupons to magnesium in natural Pacific sea water at 40°C for 140 days. In the uncoupled state in tapwater or natural sea water, the moisture uptake was -0.85% and calcerous deposit was 0.14% and 0.36%, respectively. For the coupled materials, the moisture uptake was -1.3% and the calcerous deposit was 16%. There was some leaching loss from the coupled material. The shear strengths in four point bend tests showed negligible degradation for the soaked samples, but a 30% reduction was measured for electrically coupled materials. This reduction was correlated to delaminations, reducing the effective specimen width by 20-40%. [Pg.256]

Because magnesium has only three stable isotopes, double-spiking techniques cannot be employed to study magnesium isotopic fractionation by MC-TIMS. However, this is possible using MC-ICP-MS, which yielded clear evidence for isotope fractionation effects for magnesium in Nature [218-220]. However, no such measurements have been conducted so far in humans, although significant isotope fractionation effects similar to those observed for calcium can clearly be expected. [Pg.471]

Boron does not occur free in nature in minerals, it occurs as borates, for example, kernite. Na2B407.4H2O. and borax. Na2B407. IOH2O there are extensive deposits of these in the USA. Boron can be obtained by heating boron trioxide with magnesium ... [Pg.141]

Magnesium sulfate [7487-88-9] MgSO, is found widely in nature as either a double salt or as a hydrate. The more important mineral forms are Hsted in Table 23. [Pg.356]

The recovery of vanadium from these slags is of commercial interest because of the depletion of easily accessible ores and the comparatively low concentrations (ranging from less than 100 ppm to 500 ppm) of vanadium in natural deposits (147,148). In the LILCO appHcations the total ash contained up to 36% 20 (147). Vanadium is of value in the manufacture of high strength steels and specialized titanium alloys used in the aerospace industry (148,149). Magnesium vanadates allow the recovery of vanadium as a significant by-product of fuel use by electric utiUties (see Recycling, nonferrous LffiTALS). [Pg.360]

Forsterite. Pure forsterite is rare in nature. Most natural magnesium orthosiUcates form soHd solutions of fayaUte, Fe2Si04, and forsterite. Forsterite refractories are usually made by calcining magnesium siUcate rock such as dunite, serpentine, or oHvine with sufficient magnesia added to convert all excess siUca to forsterite and all sesquioxides to magnesia spinels. [Pg.26]

Sodium nitrate nitrate [7631-99-4] NaNO, is found in naturally occurring deposits associated with sodium chloride, sodium sulfate, potassium chloride, potassium nitrate, magnesium chloride, and other salts. Accumulations of sodium nitrate have been reported in several countries, but the only ones being commercially exploited are the unique nitrate-rich deposits in Chile, South America. Natural sodium nitrate is also referred to as Chilean saltpeter or Chilean nitrate. [Pg.192]

Calcium [7440-70-2J, Ca, a member of Group 2 (IIA) of the Periodic Table between magnesium and strontium, is classified, together with barium and strontium, as an alkaline-earth metal and is the lightest of the three. Calcium metal does not occur free in nature however, in the form of numerous compounds, it is the fifth most abundant element constituting 3.63% of the earth s cmst. [Pg.399]

Magnesium. This molten salt electrolysis process is the current principal method of magnesium production. The graphite anodes can be either round or rectangular in nature (see Magnesiumand magnesium alloys). [Pg.521]

Lime is among a family of chemicals which are alkaline in nature and contain principally calcium, oxygen and, in some cases, magnesium. In this grouping are included quicklime, dolomitic lime, hydrated lime, dolomitic hydrated lime, limestone, and dolomite. The most commonly used additives are quicklime and hydrated lime, but the dolomitic counterparts of these chemicals (i.e., the high-magnesium forms) are also widely used in wastewater treatment and are generally similar in physical requirements. [Pg.101]

Carbon dioxide and calcium carbonate The effect of carbon dioxide is closely linked with the bicarbonate content. Normal carbonates are rarely found in natural waters but sodium bicarbonate is found in some underground supplies. Calcium bicarbonate is the most important, but magnesium bicarbonate may be present in smaller quantities in general, it may be regarded as having properties similar to those of the calcium compound except that on decomposition by heat it deposits magnesium hydroxide whereas calcium bicarbonate precipitates the carbonate. [Pg.350]

Dissolved mineral salts The principal ions found in water are calcium, magnesium, sodium, bicarbonate, sulphate, chloride and nitrate. A few parts per million of iron or manganese may sometimes be present and there may be traces of potassium salts, whose behaviour is very similar to that of sodium salts. From the corrosion point of view the small quantities of other acid radicals present, e.g. nitrite, phosphate, iodide, bromide and fluoride, have little significance. Larger concentrations of some of these ions, notably nitrite and phosphate, may act as corrosion inhibitors, but the small quantities present in natural waters will have little effect. Some of the minor constituents have other beneficial or harmful effects, e.g. there is an optimum concentration of fluoride for control of dental caries and very low iodide or high nitrate concentrations are objectionable on medical grounds. [Pg.354]

Whilst cathodic protection can be used to protect most metals from aqueous corrosion, it is most commonly applied to carbon steel in natural environments (waters, soils and sands). In a cathodic protection system the sacrificial anode must be more electronegative than the structure. There is, therefore, a limited range of suitable materials available to protect carbon steel. The range is further restricted by the fact that the most electronegative metals (Li, Na and K) corrode extremely rapidly in aqueous environments. Thus, only magnesium, aluminium and zinc are viable possibilities. These metals form the basis of the three generic types of sacrificial anode. [Pg.138]

Magnesium (eighth most abundant element) is found principally as Mg+2 ion in salt deposits, particularly as the slightly soluble carbonate, MgC03, and also in sea water. The element is oxidized by atmospheric oxygen and is not found in an uncombined state in nature. [Pg.373]

Magnesium. Mg, at wt 24.312, at no 12, valence 2. Isotopes 24 (77.4%), 25 (11.5%) 26 (11.1%). Physical properties of 99.9% pure Mg are (riven in the fnllnwino tsKle fRef 10 n 6791 Mg is very abundant in nature, occurring in substantial amounts in many rock-forming minerals such as dolomite, magnesite, olivine, and serpentine. In addition, it is also found in sea water, subterranean brines, and salt beds. [Pg.21]

Magnesium concentration in natural waters and ground-water... [Pg.464]

The extraction of metals fundamentally relies on their availability in nature. Three terms are important while one refers to availability. One is the crustal abundance and the other two are the terms resources and reserves. The average crustal abundance of the most abundant metals, aluminum, iron and magnesium, are 8.1%, 5.0% and 2.1% respectively. Among the rare metals titanium is the most abundant, constituting 0.53% of the Earth s crust No metal can be economically extracted from a source in which its concentration is the same... [Pg.2]


See other pages where Magnesium in nature is mentioned: [Pg.713]    [Pg.354]    [Pg.355]    [Pg.411]    [Pg.412]    [Pg.69]    [Pg.455]    [Pg.713]    [Pg.354]    [Pg.355]    [Pg.411]    [Pg.412]    [Pg.69]    [Pg.455]    [Pg.233]    [Pg.220]    [Pg.313]    [Pg.343]    [Pg.352]    [Pg.13]    [Pg.178]    [Pg.204]    [Pg.459]    [Pg.142]    [Pg.232]    [Pg.660]    [Pg.424]    [Pg.367]    [Pg.125]    [Pg.391]    [Pg.6]    [Pg.555]    [Pg.58]    [Pg.69]    [Pg.91]    [Pg.115]    [Pg.385]    [Pg.440]   
See also in sourсe #XX -- [ Pg.869 ]




SEARCH



© 2024 chempedia.info