|Appearance||shiny grey solid|
|Standard atomic weight Ar, std(Mg)||[24.304, 24.307] conventional: 24.305|
|Magnesium in the periodic table|
|Atomic number (Z)||12|
|Group||group 2 (alkaline earth metals)|
|Electron configuration||[Ne] 3s2|
|Electrons per shell||2, 8, 2|
|Phase at STP||solid|
|Melting point||923 K (650 °C, 1202 °F)|
|Boiling point||1363 K (1091 °C, 1994 °F)|
|Density (near r.t.)||1.738 g/cm3|
|when liquid (at m.p.)||1.584 g/cm3|
|Heat of fusion||8.48 kJ/mol|
|Heat of vaporization||128 kJ/mol|
|Molar heat capacity||24.869 J/(mol·K)|
|Oxidation states||+1, +2 (a strongly basic oxide)|
|Electronegativity||Pauling scale: 1.31|
|Atomic radius||empirical: 160 pm|
|Covalent radius||141±7 pm|
|Van der Waals radius||173 pm|
|Spectral lines of magnesium|
|Crystal structure||hexagonal close-packed (hcp)|
|Speed of sound thin rod||4940 m/s (at r.t.) (annealed)|
|Thermal expansion||24.8 µm/(m·K) (at 25 °C)|
|Thermal conductivity||156 W/(m·K)|
|Electrical resistivity||43.9 nΩ·m (at 20 °C)|
|Magnetic susceptibility||+13.1·10−6 cm3/mol (298 K)|
|Young's modulus||45 GPa|
|Shear modulus||17 GPa|
|Bulk modulus||35.4 GPa|
|Brinell hardness||44–260 MPa|
|Naming||after Magnesia, Greece|
|Discovery||Joseph Black (1755)|
|First isolation||Humphry Davy (1808)|
|Main isotopes of magnesium|
Magnesium is a chemical element with the symbol Mg and atomic number 12. It is a shiny gray solid which bears a close physical resemblance to the other five elements in the second column (group 2, or alkaline earth metals) of the periodic table: all group 2 elements have the same electron configuration in the outer electron shell and a similar crystal structure.
Magnesium is the ninth most abundant element in the universe. It is produced in large, aging stars from the sequential addition of three helium nuclei to a carbon nucleus. When such stars explode as supernovas, much of the magnesium is expelled into the interstellar medium where it may recycle into new star systems. Magnesium is the eighth most abundant element in the Earth's crust and the fourth most common element in the Earth (after iron, oxygen and silicon), making up 13% of the planet's mass and a large fraction of the planet's mantle. It is the third most abundant element dissolved in seawater, after sodium and chlorine.
Magnesium occurs naturally only in combination with other elements, where it invariably has a +2 oxidation state. The free element (metal) can be produced artificially, and is highly reactive (though in the atmosphere it is soon coated in a thin layer of oxide that partly inhibits reactivity – see passivation). The free metal burns with a characteristic brilliant-white light. The metal is now obtained mainly by electrolysis of magnesium salts obtained from brine, and is used primarily as a component in aluminium-magnesium alloys, sometimes called magnalium or magnelium. Magnesium is less dense than aluminium, and the alloy is prized for its combination of lightness and strength.
Magnesium is the eleventh most abundant element by mass in the human body and is essential to all cells and some 300 enzymes. Magnesium ions interact with polyphosphate compounds such as ATP, DNA, and RNA. Hundreds of enzymes require magnesium ions to function. Magnesium compounds are used medicinally as common laxatives, antacids (e.g., milk of magnesia), and to stabilize abnormal nerve excitation or blood vessel spasm in such conditions as eclampsia.
Elemental magnesium is a gray-white lightweight metal, two-thirds the density of aluminium. Magnesium has the lowest melting (923 K (1,202 °F)) and the lowest boiling point 1,363 K (1,994 °F) of all the alkaline earth metals.
Pure polycrystalline magnesium is brittle and easily fractures along shear bands. It becomes much more ductile when alloyed with small amount of other metals, such as 1% aluminium. Ductility of polycrystalline magnesium can also be significantly improved by reducing its grain size to ca. 1 micron or less.
It tarnishes slightly when exposed to air, although, unlike the heavier alkaline earth metals, an oxygen-free environment is unnecessary for storage because magnesium is protected by a thin layer of oxide that is fairly impermeable and difficult to remove.
Magnesium reacts with water at room temperature, though it reacts much more slowly than calcium, a similar group 2 metal. When submerged in water, hydrogen bubbles form slowly on the surface of the metal – though, if powdered, it reacts much more rapidly. The reaction occurs faster with higher temperatures (see safety precautions). Magnesium's reversible reaction with water can be harnessed to store energy and run a magnesium-based engine. Magnesium also reacts exothermically with most acids such as hydrochloric acid (HCl), producing the metal chloride and hydrogen gas, similar to the HCl reaction with aluminium, zinc, and many other metals.
Magnesium is highly flammable, especially when powdered or shaved into thin strips, though it is difficult to ignite in mass or bulk. Flame temperatures of magnesium and magnesium alloys can reach 3,100 °C (5,610 °F), although flame height above the burning metal is usually less than 300 mm (12 in). Once ignited, such fires are difficult to extinguish, because combustion continues in nitrogen (forming magnesium nitride), carbon dioxide (forming magnesium oxide and carbon), and water (forming magnesium oxide and hydrogen, which also combusts due to heat in the presence of additional oxygen). This property was used in incendiary weapons during the firebombing of cities in World War II, where the only practical civil defense was to smother a burning flare under dry sand to exclude atmosphere from the combustion.
Magnesium may also be used as an igniter for thermite, a mixture of aluminium and iron oxide powder that ignites only at a very high temperature.
Organomagnesium compounds are widespread in organic chemistry. They are commonly found as Grignard reagents. Magnesium can react with haloalkanes to give Grignard reagents. Examples of Grignard reagents are phenylmagnesium bromide and ethylmagnesium bromide. The Grignard reagents function as a common nucleophile, attacking the electrophilic group such as the carbon atom that is present within the polar bond of a carbonyl group.
A prominent organomagnesium reagent beyond Grignard reagents is magnesium anthracene with magnesium forming a 1,4-bridge over the central ring. It is used as a source of highly active magnesium. The related butadiene-magnesium adduct serves as a source for the butadiene dianion.
Source of light
When burning in air, magnesium produces a brilliant-white light that includes strong ultraviolet wavelengths. Magnesium powder (flash powder) was used for subject illumination in the early days of photography. Later, magnesium filament was used in electrically ignited single-use photography flashbulbs. Magnesium powder is used in fireworks and marine flares where a brilliant white light is required. It was also used for various theatrical effects, such as lightning, pistol flashes, and supernatural appearances.
Magnesium is the eighth-most-abundant element in the Earth's crust by mass and tied in seventh place with iron in molarity. It is found in large deposits of magnesite, dolomite, and other minerals, and in mineral waters, where magnesium ion is soluble.
cation is the second-most-abundant cation in seawater (about ⅛ the mass of sodium ions in a given sample), which makes seawater and sea salt attractive commercial sources for Mg. To extract the magnesium, calcium hydroxide is added to seawater to form magnesium hydroxide precipitate.
2 + Ca(OH)
2 → Mg(OH)
2 + CaCl
2 + 2 HCl → MgCl
2 + 2 H
From magnesium chloride, electrolysis produces magnesium.
As of 2013, magnesium alloys consumption was less than one million tonnes per year, compared with 50 million tonnes of aluminum alloys. Their use has been historically limited by the tendency of Mg alloys to corrode, creep at high temperatures, and combust.
The presence of iron, nickel, copper, and cobalt strongly activates corrosion. In more than trace amounts, these metals precipitate as intermetallic compounds, and the precipitate locales function as active cathodic sites that reduce water, causing the loss of magnesium. Controlling the quantity of these metals improves corrosion resistance. Sufficient manganese overcomes the corrosive effects of iron. This requires precise control over composition, increasing costs. Adding a cathodic poison captures atomic hydrogen within the structure of a metal. This prevents the formation of free hydrogen gas, an essential factor of corrosive chemical processes. The addition of about one in three hundred parts arsenic reduces its corrosion rate in a salt solution by a factor of nearly ten.
High-temperature creep and flammability
Research showed that magnesium's tendency to creep at high temperatures is eliminated by the addition of scandium and gadolinium. Flammability is greatly reduced by a small amount of calcium in the alloy. Recent research has indicated that by using rare-earth elements, it may be possible to manufacture magnesium alloys with an ignition temperature higher than magnesium's liquidus and in some cases potentially pushing it close to magnesium's boiling point.
Magnesium forms a variety of compounds important to industry and biology, including magnesium carbonate, magnesium chloride, magnesium citrate, magnesium hydroxide (milk of magnesia), magnesium oxide, magnesium sulfate, and magnesium sulfate heptahydrate (Epsom salts).
Magnesium has three stable isotopes: 24
Mg and 26
Mg. All are present in significant amounts (see table of isotopes above). About 79% of Mg is 24
Mg. The isotope 28
Mg is radioactive and in the 1950s to 1970s was produced by several nuclear power plants for use in scientific experiments. This isotope has a relatively short half-life (21 hours) and its use was limited by shipping times.
The nuclide 26
Mg has found application in isotopic geology, similar to that of aluminium. 26
Mg is a radiogenic daughter product of 26
Al, which has a half-life of 717,000 years. Excessive quantities of stable 26
Mg have been observed in the Ca-Al-rich inclusions of some carbonaceous chondrite meteorites. This anomalous abundance is attributed to the decay of its parent 26
Al in the inclusions, and researchers conclude that such meteorites were formed in the solar nebula before the 26
Al had decayed. These are among the oldest objects in the solar system and contain preserved information about its early history.
It is conventional to plot 26
Mg against an Al/Mg ratio. In an isochron dating plot, the Al/Mg ratio plotted is27
Mg. The slope of the isochron has no age significance, but indicates the initial 26
Al ratio in the sample at the time when the systems were separated from a common reservoir.
World production was approximately 1,100 kt in 2017, with the bulk being produced in China (930 kt) and Russia (60 kt). China is almost completely reliant on the silicothermic Pidgeon process (the reduction of the oxide at high temperatures with silicon, often provided by a ferrosilicon alloy in which the iron is but a spectator in the reactions) to obtain the metal. The process can also be carried out with carbon at approx 2300 °C:
(s) + Si
(s) + 2CaO
(s) → 2Mg
(g) + Ca
(s) + C
(s) → Mg
(g) + CO
In the United States, magnesium is obtained principally with the Dow process, by electrolysis of fused magnesium chloride from brine and sea water. A saline solution containing Mg2+
ions is first treated with lime (calcium oxide) and the precipitated magnesium hydroxide is collected:
(aq) + CaO
(s) + H
2O → Ca2+
(aq) + Mg(OH)
2(s) + 2 HCl → MgCl
2(aq) + 2H
- 2 Cl−
2 (g) + 2
A new process, solid oxide membrane technology, involves the electrolytic reduction of MgO. At the cathode, Mg2+
ion is reduced by two electrons to magnesium metal. The electrolyte is yttria-stabilized zirconia (YSZ). The anode is a liquid metal. At the YSZ/liquid metal anode O2−
is oxidized. A layer of graphite borders the liquid metal anode, and at this interface carbon and oxygen react to form carbon monoxide. When silver is used as the liquid metal anode, there is no reductant carbon or hydrogen needed, and only oxygen gas is evolved at the anode. It has been reported that this method provides a 40% reduction in cost per pound over the electrolytic reduction method. This method is more environmentally sound than others because there is much less carbon dioxide emitted.
The United States has traditionally been the major world supplier of this metal, supplying 45% of world production even as recently as 1995. Today, the US market share is at 7%, with a single domestic producer left, US Magnesium, a Renco Group company in Utah born from now-defunct Magcorp.
The name magnesium originates from the Greek word for locations related to the tribe of the Magnetes, either a district in Thessaly called Magnesia or Magnesia ad Sipylum, now in Turkey. It is related to magnetite and manganese, which also originated from this area, and required differentiation as separate substances. See manganese for this history.
In 1618, a farmer at Epsom in England attempted to give his cows water from a well there. The cows refused to drink because of the water's bitter taste, but the farmer noticed that the water seemed to heal scratches and rashes. The substance became known as Epsom salts and its fame spread. It was eventually recognized as hydrated magnesium sulfate, MgSO
The metal itself was first isolated by Sir Humphry Davy in England in 1808. He used electrolysis on a mixture of magnesia and mercuric oxide. Antoine Bussy prepared it in coherent form in 1831. Davy's first suggestion for a name was magnium, but the name magnesium is now used.
Uses as a metal
Magnesium is the third-most-commonly-used structural metal, following iron and aluminium. The main applications of magnesium are, in order: aluminium alloys, die-casting (alloyed with zinc), removing sulfur in the production of iron and steel, and the production of titanium in the Kroll process. Magnesium is used in super-strong, lightweight materials and alloys. For example, when infused with silicon carbide nanoparticles, it has extremely high specific strength.
Historically, magnesium was one of the main aerospace construction metals and was used for German military aircraft as early as World War I and extensively for German aircraft in World War II. The Germans coined the name "Elektron" for magnesium alloy, a term which is still used today. In the commercial aerospace industry, magnesium was generally restricted to engine-related components, due to fire and corrosion hazards. Currently, magnesium alloy use in aerospace is increasing, driven by the importance of fuel economy. Development and testing of new magnesium alloys continues, notably Elektron 21, which (in test) has proved suitable for aerospace engine, internal, and airframe components. The European Community runs three R&D magnesium projects in the Aerospace priority of Six Framework Program. Recent developments in metallurgy and maufacturing have allowed for the potential for magnesium alloys to act as replacements for aluminium and steel alloys in certain applications.
In the form of thin ribbons, magnesium is used to purify solvents; for example, preparing super-dry ethanol.
- Wright Aeronautical used a magnesium crankcase in the WWII-era Wright R-3350 Duplex Cyclone aviation engine. This presented a serious problem for the earliest models of the Boeing B-29 Superfortress heavy bomber when an in-flight engine fire ignited the engine crankcase. The resulting combustion was as hot as 5,600 °F (3,100 °C) and could sever the wing spar from the fuselage.
- Mercedes-Benz used the alloy Elektron in the bodywork of an early model Mercedes-Benz 300 SLR; these cars competed in the 1955 World Sportscar Championship including a win at the Mille Miglia, and at Le Mans where one was involved in the 1955 Le Mans disaster when spectators were showered with burning fragments of elektron.
- Porsche used magnesium alloy frames in the 917/053 that won Le Mans in 1971, and continues to use magnesium alloys for its engine blocks due to the weight advantage.
- Volkswagen Group has used magnesium in its engine components for many years.
- Mitsubishi Motors uses magnesium for its paddle shifters.
- BMW used magnesium alloy blocks in their N52 engine, including an aluminium alloy insert for the cylinder walls and cooling jackets surrounded by a high-temperature magnesium alloy AJ62A. The engine was used worldwide between 2005 and 2011 in various 1, 3, 5, 6, and 7 series models; as well as the Z4, X1, X3, and X5.
- Chevrolet used the magnesium alloy AE44 in the 2006 Corvette Z06.
Both AJ62A and AE44 are recent developments in high-temperature low-creep magnesium alloys. The general strategy for such alloys is to form intermetallic precipitates at the grain boundaries, for example by adding mischmetal or calcium. New alloy development and lower costs that make magnesium competitive with aluminium will increase the number of automotive applications.
Because of low density and good mechanical and electrical properties, magnesium is widely used for manufacturing of mobile phones, laptop and tablet computers, cameras, and other electronic components.
Magnesium, being readily available and relatively nontoxic, has a variety of uses:
- Magnesium is flammable, burning at a temperature of approximately 3,100 °C (3,370 K; 5,610 °F), and the autoignition temperature of magnesium ribbon is approximately 473 °C (746 K; 883 °F). It produces intense, bright, white light when it burns. Magnesium's high combustion temperature makes it a useful tool for starting emergency fires. Other uses include flash photography, flares, pyrotechnics, fireworks sparklers, and trick birthday candles. Magnesium is also often used to ignite thermite or other materials that require a high ignition temperature.
- In the form of turnings or ribbons, to prepare Grignard reagents, which are useful in organic synthesis.
- As an additive agent in conventional propellants and the production of nodular graphite in cast iron.
- As a reducing agent to separate uranium and other metals from their salts.
- As a sacrificial (galvanic) anode to protect boats, underground tanks, pipelines, buried structures, and water heaters.
- Alloyed with zinc to produce the zinc sheet used in photoengraving plates in the printing industry, dry-cell battery walls, and roofing.
- As a metal, this element's principal use is as an alloying additive to aluminium with these aluminium-magnesium alloys being used mainly for beverage cans, sports equipment such as golf clubs, fishing reels, and archery bows and arrows.
- Specialty, high-grade car wheels of magnesium alloy are called "mag wheels", although the term is often misapplied to aluminium wheels. Many car and aircraft manufacturers have made engine and body parts from magnesium.
- Magnesium batteries have been commercialized as primary batteries, and are an active topic of research for rechargeable batteries.
|GHS Signal word||Danger|
|H228, H251, H261|
|P210, P231, P235, P410, P422|
|NFPA 704 (fire diamond)|
Magnesium metal and its alloys can be explosive hazards; they are highly flammable in their pure form when molten or in powder or ribbon form. Burning or molten magnesium reacts violently with water. When working with powdered magnesium, safety glasses with eye protection and UV filters (such as welders use) are employed because burning magnesium produces ultraviolet light that can permanently damage the retina of a human eye.
- Mg (s) + 2 H
2O (l) → Mg(OH)
2 (s) + H
Therefore, water cannot extinguish magnesium fires. The hydrogen gas produced intensifies the fire. Dry sand is an effective smothering agent, but only on relatively level and flat surfaces.
- 2 Mg + CO
2 → 2 MgO + C (s)
Hence, carbon dioxide fuels rather than extinguishes magnesium fires.
Magnesium compounds, primarily magnesium oxide (MgO), are used as a refractory material in furnace linings for producing iron, steel, nonferrous metals, glass, and cement. Magnesium oxide and other magnesium compounds are also used in the agricultural, chemical, and construction industries. Magnesium oxide from calcination is used as an electrical insulator in fire-resistant cables.
Magnesium hydride is under investigation as a way to store hydrogen.
Magnesium phosphate is used to fireproof wood used in construction.
Magnesium hexafluorosilicate is used for moth-proofing textiles.
Mechanism of action
The important interaction between phosphate and magnesium ions makes magnesium essential to the basic nucleic acid chemistry of all cells of all known living organisms. More than 300 enzymes require magnesium ions for their catalytic action, including all enzymes using or synthesizing ATP and those that use other nucleotides to synthesize DNA and RNA. The ATP molecule is normally found in a chelate with a magnesium ion.
In the UK, the recommended daily values for magnesium are 300 mg for men and 270 mg for women. In the U.S. the Recommended Dietary Allowances (RDAs) are 400 mg for men ages 19–30 and 420 mg for older; for women 310 mg for ages 19–30 and 320 mg for older.
Numerous pharmaceutical preparations of magnesium and dietary supplements are available. In two human trials magnesium oxide, one of the most common forms in magnesium dietary supplements because of its high magnesium content per weight, was less bioavailable than magnesium citrate, chloride, lactate or aspartate.
An adult body has 22–26 grams of magnesium, with 60% in the skeleton, 39% intracellular (20% in skeletal muscle), and 1% extracellular. Serum levels are typically 0.7–1.0 mmol/L or 1.8–2.4 mEq/L. Serum magnesium levels may be normal even when intracellular magnesium is deficient. The mechanisms for maintaining the magnesium level in the serum are varying gastrointestinal absorption and renal excretion. Intracellular magnesium is correlated with intracellular potassium. Increased magnesium lowers calcium and can either prevent hypercalcemia or cause hypocalcemia depending on the initial level. Both low and high protein intake conditions inhibit magnesium absorption, as does the amount of phosphate, phytate, and fat in the gut. Unabsorbed dietary magnesium is excreted in feces; absorbed magnesium is excreted in urine and sweat.
Detection in serum and plasma
Magnesium status may be assessed by measuring serum and erythrocyte magnesium concentrations coupled with urinary and fecal magnesium content, but intravenous magnesium loading tests are more accurate and practical. A retention of 20% or more of the injected amount indicates deficiency. No biomarker has been established for magnesium.
Magnesium concentrations in plasma or serum may be monitored for efficacy and safety in those receiving the drug therapeutically, to confirm the diagnosis in potential poisoning victims, or to assist in the forensic investigation in a case of fatal overdose. The newborn children of mothers who received parenteral magnesium sulfate during labor may exhibit toxicity with normal serum magnesium levels.
Low plasma magnesium (hypomagnesemia) is common: it is found in 2.5–15% of the general population. From 2005 to 2006, 48 percent of the United States population consumed less magnesium than recommended in the Dietary Reference Intake. Other causes are increased renal or gastrointestinal loss, an increased intracellular shift, and proton-pump inhibitor antacid therapy. Most are asymptomatic, but symptoms referable to neuromuscular, cardiovascular, and metabolic dysfunction may occur. Alcoholism is often associated with magnesium deficiency. Chronically low serum magnesium levels are associated with metabolic syndrome, diabetes mellitus type 2, fasciculation, and hypertension.
- Intravenous magnesium is recommended by the ACC/AHA/ESC 2006 Guidelines for Management of Patients With Ventricular Arrhythmias and the Prevention of Sudden Cardiac Death for patients with ventricular arrhythmia associated with torsades de pointes who present with long QT syndrome; and for the treatment of patients with digoxin induced arrhythmias.
- Magnesium sulfate – intravenous – is used for the management of pre-eclampsia and eclampsia.
- Hypomagnesemia, including that caused by alcoholism, is reversible by oral or parenteral magnesium administration depending on the degree of deficiency.
- There is limited evidence that magnesium supplementation may play a role in the prevention and treatment of migraine.
Sorted by type of magnesium salt, other therapeutic applications include:
- Magnesium sulfate, as the heptahydrate called Epsom salts, is used as bath salts, a laxative, and a highly soluble fertilizer.
- Magnesium hydroxide, suspended in water, is used in milk of magnesia antacids and laxatives.
- Magnesium chloride, oxide, gluconate, malate, orotate, glycinate, ascorbate and citrate are all used as oral magnesium supplements.
- Magnesium borate, magnesium salicylate, and magnesium sulfate are used as antiseptics.
- Magnesium bromide is used as a mild sedative (this action is due to the bromide, not the magnesium).
- Magnesium stearate is a slightly flammable white powder with lubricating properties. In pharmaceutical technology, it is used in pharmacological manufacture to prevent tablets from sticking to the equipment while compressing the ingredients into tablet form.
- Magnesium carbonate powder is used by athletes such as gymnasts, weightlifters, and climbers to eliminate palm sweat, prevent sticking, and improve the grip on gymnastic apparatus, lifting bars, and climbing rocks.
Overdose from dietary sources alone is unlikely because excess magnesium in the blood is promptly filtered by the kidneys, and overdose is more likely in the presence of impaired renal function. In spite of this, megadose therapy has caused death in a young child, and severe hypermagnesemia in a woman and a young girl who had healthy kidneys. The most common symptoms of overdose are nausea, vomiting, and diarrhea; other symptoms include hypotension, confusion, slowed heart and respiratory rates, deficiencies of other minerals, coma, cardiac arrhythmia, and death from cardiac arrest.
Function in plants
Plants require magnesium to synthesize chlorophyll, essential for photosynthesis. Magnesium in the center of the porphyrin ring in chlorophyll functions in a manner similar to the iron in the center of the porphyrin ring in heme. Magnesium deficiency in plants causes late-season yellowing between leaf veins, especially in older leaves, and can be corrected by either applying epsom salts (which is rapidly leached), or crushed dolomitic limestone, to the soil.
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