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Magnesium carbonate, MgCO3 (archaic name magnesia alba), is an inorganic salt that is a colourless or white solid. Several hydrated and basic forms of magnesium carbonate also exist as minerals.
Forms
The most common magnesium carbonate forms are the anhydrous salt called magnesite (MgCO3), and the di, tri, and pentahydrates known as barringtonite (MgCO3·2H2O), nesquehonite (MgCO3·3H2O), and lansfordite (MgCO3·5H2O), respectively.[6] Some basic forms such as artinite (Mg2CO3(OH)2·3H2O), hydromagnesite (Mg5(CO3)4(OH)2·4H2O), and dypingite (Mg5(CO3)4(OH)2·5H2O) also occur as minerals. All of those minerals are colourless or white.
The dihydrate has a triclinic structure, while the trihydrate has a monoclinic structure.
References to "light" and "heavy" magnesium carbonates actually refer to the magnesium hydroxy carbonates hydromagnesite and dypingite, respectively.[7] The "light" form is precipitated from magnesium solutions using alkali carbonate at "normal temperatures" while the "heavy" may be produced from boiling concentrated solutions followed by precipitation to dryness, washing of the precipitate, and drying at 100 C. [8]
Preparation
Magnesium carbonate is ordinarily obtained by mining the mineral magnesite. Seventy percent of the world's supply is mined and prepared in China.[9]
Magnesium carbonate can be prepared in laboratory by reaction between any soluble magnesium salt and sodium bicarbonate:
If magnesium chloride (or sulfate) is treated with aqueous sodium carbonate, a precipitate of basic magnesium carbonate – a hydrated complex of magnesium carbonate and magnesium hydroxide – rather than magnesium carbonate itself is formed:
High purity industrial routes include a path through magnesium bicarbonate, which can be formed by combining a slurry of magnesium hydroxide and carbon dioxide at high pressure and moderate temperature.[6] The bicarbonate is then vacuum dried, causing it to lose carbon dioxide and a molecule of water:
Mg(OH)2 + 2 CO2 → Mg(HCO3)2
Mg(HCO3)2 → MgCO3 + CO2 + H2O
Chemical properties
With acids
Like many common group 2 metal carbonates, magnesium carbonate reacts with aqueous acids to release carbon dioxide and water:
MgCO3 + 2 HCl → MgCl2 + CO2 + H2O
MgCO3 + H2SO4 → MgSO4 + CO2 + H2O
Decomposition
At high temperatures MgCO3 decomposes to magnesium oxide and carbon dioxide. This process is important in the production of magnesium oxide.[6] This process is called calcining:
MgCO3 → MgO + CO2 (ΔH = +118 kJ/mol)
The decomposition temperature is given as 350°C (662°F).[10][11] However, calcination to the oxide is generally not considered complete below 900°C due to interfering readsorption of liberated carbon dioxide.
The hydrates of the salts lose water at different temperatures during decomposition.[12] For example, in the trihydrate MgCO3·3H2O, which molecular formula may be written as Mg(HCO3)(OH)·2H2O, the dehydration steps occur at 157°C and 179°C as follows:[12]
Mg(HCO3)(OH)·2(H2O) → Mg(HCO3)(OH)·(H2O) + H2O at 157 °C
Because of its low solubility in water and hygroscopic properties, MgCO3 was first added to table salt (NaCl) in 1911 to make it flow more freely. The Morton Salt company adopted the slogan "When it rains it pours", highlighting that its salt, which contained MgCO3, would not stick together in humid weather.[13]
Climber Jan Hojer blows surplus chalk from his hand. Boulder World Cup 2015
Powdered magnesium carbonate, known as climbing chalk or gym chalk is also used as a drying agent on athletes' hands in rock climbing, gymnastics, powerlifting, weightlifting and other sports in which a firm grip is necessary.[9] A variant is liquid chalk.
As a food additive, magnesium carbonate is known as E504. Its only known side effect is that it may work as a laxative in high concentrations.[14]
Magnesium carbonate is used in taxidermy for whitening skulls. It can be mixed with hydrogen peroxide to create a paste, which is spread on the skull to give it a white finish.
In addition, high purity magnesium carbonate is used as an antacid and as an additive in table salt to keep it free flowing. Magnesium carbonate can do this because it does not dissolve in water, only in acid, where it will effervesce (bubble).[16]
Safety
Magnesium carbonate is non-toxic and non-flammable.
↑ Bénézeth, Pascale; Saldi, Giuseppe D.; Dandurand, Jean-Louis; Schott, Jacques (2011). "Experimental determination of the solubility product of magnesite at 50 to 200°C". Chemical Geology. 286 (1–2): 21–31. Bibcode:2011ChGeo.286...21B. doi:10.1016/j.chemgeo.2011.04.016.
↑ J.R. Partington (1951). General and inorganic chemistry, 2nd ed.
1 2 Allf, Bradley (21 May 2018). "The Hidden Environmental Cost of Climbing Chalk". Climbing Magazine. Cruz Bay Publishing. Retrieved 22 May 2018. In fact, China produces 70 percent of the world's magnesite. Most of that production—both mining and processing—is concentrated in a small corner of Liaoning, a hilly industrial province in northeast China between Beijing and North Korea.
↑ British Pharmacopoeia Commission Secretariat (2009). "Index, BP 2009"(PDF). Archived from the original(PDF) on 11 April 2009. Retrieved 31 January 2010.
A carbonate is a salt of carbonic acid,, characterized by the presence of the carbonate ion, a polyatomic ion with the formula CO2−3. The word "carbonate" may also refer to a carbonate ester, an organic compound containing the carbonate groupO=C(−O−)2.
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Weathering is the deterioration of rocks, soils and minerals through contact with water, atmospheric gases, sunlight, and biological organisms. It occurs in situ, and so is distinct from erosion, which involves the transport of rocks and minerals by agents such as water, ice, snow, wind, waves and gravity.
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Sodium carbonate is the inorganic compound with the formula Na2CO3 and its various hydrates. All forms are white, odourless, water-soluble salts that yield alkaline solutions in water. Historically, it was extracted from the ashes of plants grown in sodium-rich soils, and because the ashes of these sodium-rich plants were noticeably different from ashes of wood, sodium carbonate became known as "soda ash". It is produced in large quantities from sodium chloride and limestone by the Solvay process, as well as by carbonating sodium hydroxide which is made using the chloralkali process.
Calcium hydroxide (traditionally called slaked lime) is an inorganic compound with the chemical formula Ca(OH)2. It is a colorless crystal or white powder and is produced when quicklime (calcium oxide) is mixed with water. Annually, approximately 125 million tons of calcium hydroxide are produced worldwide.
Magnesite is a mineral with the chemical formula MgCO 3. Iron, manganese, cobalt, and nickel may occur as admixtures, but only in small amounts.
The Solvay process or ammonia–soda process is the major industrial process for the production of sodium carbonate (soda ash, Na2CO3). The ammonia–soda process was developed into its modern form by the Belgian chemist Ernest Solvay during the 1860s. The ingredients for this are readily available and inexpensive: salt brine (from inland sources or from the sea) and limestone (from quarries). The worldwide production of soda ash in 2005 was estimated at 42 million tonnes, which is more than six kilograms (13 lb) per year for each person on Earth. Solvay-based chemical plants now produce roughly three-quarters of this supply, with the remaining being mined from natural deposits. This method superseded the Leblanc process.
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