Everything Totally Explained


Ask & we'll explain, totally!
Manganese
Totally Explained


  NEW! All the latest news in the worlds of computer gaming, entertainment, the environment,  
finance, health, politics, science, stocks & shares, technology and much, much, more.  


View this entry using RSS

Everything about Manganese totally explained

Substitutes: Manganese has no satisfactory substitute in its major applications, which are related to metallurgical alloy use. In minor applications, (for example, manganese phosphating), zinc and sometimes vanadium are viable substitutes. In disposable battery manufacture, standard and alkaline cells using manganese will probably eventually be mostly replaced with lithium battery technology.
   The overall level and nature of manganese use in the United States is expected to remain about the same in the near term. No practical technologies exist for replacing manganese with other materials or for using domestic deposits or other accumulations to reduce the complete dependence of the United States on other countries for manganese ore.

Metal alloys

Manganese is essential to iron and steel production by virtue of its sulfur-fixing, deoxidizing, and alloying properties. Steelmaking, including its ironmaking component, has accounted for most manganese demand, presently in the range of 85% to 90% of the total demand. Among a variety of other uses, manganese is a key component of low-cost stainless steel formulations and certain widely used aluminium alloys.
   The metal is very occasionally used in coins; the only United States coins to use manganese were the "wartime" nickel from 1942–1945, and, since 2000, dollar coins. The EU uses manganese in 1 and 2 Euro coins, due to greater and cheaper availability.

History

The origin of the name manganese is complex. In ancient times, two black minerals from Magnesia in what is now modern Greece were both called magnes, but were thought to differ in gender. The male magnes attracted iron, and was the iron ore we now know as lodestone or magnetite, and which probably gave us the term magnet. The female magnes ore didn't attract iron, but was used to decolorize glass. This feminine magnes was later called magnesia, known now in modern times as pyrolusite or manganese dioxide. This mineral is never magnetic (although manganese itself is paramagnetic). In the 16th century, the latter compound was called manganesum (note the two n's instead of one) by glassmakers, possibly as a corruption of two words since alchemists and glassmakers eventually had to differentiate a magnesia negra (the black ore) from magnesia alba (a white ore, also from Magnesia, also useful in glassmaking). Mercati called magnesia negra Manganesa, and finally the metal isolated from it became known as manganese (German: Mangan). The name magnesia eventually was then used to refer only to the white magnesia alba (magnesium oxide), which provided the name magnesium for that free element, when it was eventually isolated, much later.
   Manganese compounds were in use in prehistoric times; paints that were pigmented with manganese dioxide can be traced back 17,000 years. The Egyptians and Romans used manganese compounds in glass-making, to either remove color from glass or add color to it. Manganese can be found in the iron ores used by the Spartans. Some speculate that the exceptional hardness of Spartan steels derives from the inadvertent production of an iron-manganese alloy.
   In the 17th century, German chemist Johann Glauber first produced permanganate, a useful laboratory reagent (although some people believe that it was discovered by Ignites Kaim in 1770). By the mid-18th century, manganese dioxide was in use in the manufacture of chlorine (which it produces when mixed with hydrochloric acid, or commercially with a mixture of dilute sulfuric acid and sodium chloride). The Swedish chemist Scheele was the first to recognize that manganese was an element, and his colleague, Johan Gottlieb Gahn, isolated the pure element in 1774 by reduction of the dioxide with carbon. Around the beginning of the 19th century, scientists began exploring the use of manganese in steelmaking, with patents being granted for its use at the time. In 1816, it was noted that adding manganese to iron made it harder, without making it any more brittle. In 1837, British academic James Couper noted an association between heavy exposure to manganese in mines with a form of Parkinson's Disease. In 1912, manganese phosphating electrochemical conversion coatings for protecting firearms against rust and corrosion were patented in the United States, and have seen widespread use ever since.
   In the 20th century, manganese dioxide has seen wide commercial use as the chief cathodic material for commercial disposable dry cells and dry batteries of both the standard (carbon-zinc) and alkaline type.

Biological role

Manganese is an essential trace nutrient in all forms of life.
   The classes of enzymes that have manganese cofactors are very broad and include such classes as oxidoreductases, transferases, hydrolases, lyases, isomerases, ligases, lectins, and integrins. The reverse transcriptases of many retroviruses (though not lentiviruses such as HIV) contain manganese. The best known manganese-containing polypeptides may be arginase, the diphtheria toxin, and Mn-containing superoxide dismutase (Mn-SOD).
   Mn-SOD is the type of SOD present in eukaryotic mitochondria, and also in most bacteria (this fact is in keeping with the bacterial-origin theory of mitochondria). The Mn-SOD enzyme is probably one of the most ancient, for nearly all organisms living in the presence of oxygen use it to deal with the toxic effects of superoxide, formed from the 1-electron reduction of dioxygen. Exceptions include a few kinds of bacteria such as Lactobacillus plantarum and related lactobacilli, which use a different non-enzymatic mechanism, involving manganese (Mn2+) ions complexed with polyphosphate directly for this task, indicating how this function possibly evolved in aerobic life.
   Manganese is also important in photosynthetic oxygen evolution in chloroplasts in plants, which are also evolutionarily of bacterial origin. The oxygen evolving complex (OEC), a water-oxidizing enzyme contained in chloroplast membrane, and which is involved in the terminal photooxidation of water during the light reactions of photosynthesis, has a metalloenzyme core containing four atoms of manganese For this reason, most broad-spectrum plant fertilizers contain manganese.

Occurrence

Manganese occurs principally as pyrolusite (MnO2), braunite, (Mn2+Mn3+6SiO12), psilomelane (Ba(Mn2+)(Mn4+)8O16(OH)4), and to a lesser extent as rhodochrosite (MnCO3). Land-based resources are large but irregularly distributed; those of the United States are very low grade and have potentially high extraction costs. Over 80% of the known world manganese resources are found in South Africa and Ukraine. Other important manganese deposits are in China, Australia, Brazil, Gabon, India, and Mexico. US Import Sources (1998-2001): Manganese ore: Gabon, 70%; South Africa, 10%; Australia, 9%; Mexico, 5%; and other, 6%. Ferromanganese: South Africa, 47%; France, 22%; Mexico, 8%; Australia, 8%; and other, 15%. Manganese contained in all manganese imports: South Africa, 31%; Gabon, 21%; Australia, 13%; Mexico, 8%; and other, 27%.
   Manganese is mined in Australia, Burkina Faso and Gabon.
   Vast quantities of manganese exist in manganese nodules on the ocean floor. Attempts to find economically viable methods of harvesting manganese nodules were abandoned in the 1970s. See also .

Isotopes

Naturally occurring manganese is composed of 1 stable isotope; 55Mn. 18 radioisotopes have been characterized with the most stable being 53Mn with a half-life of 3.7 million years, 54Mn with a half-life of 312.3 days, and 52Mn with a half-life of 5.591 days. All of the remaining radioactive isotopes have half lives that are less than 3 hours and the majority of these have half lives that are less than 1 minute. This element also has 3 meta states.
   Manganese is part of the iron group of elements which are thought to be synthesized in large stars shortly before supernova explosion. 53Mn decays to 53Cr with a half-life of 3.7 million years. Because of its relatively short half-life, 53Mn is an extinct radionuclide. Manganese isotopic contents are typically combined with chromium isotopic contents and have found application in isotope geology and radiometric dating. Mn-Cr isotopic ratios reinforce the evidence from 26Al and 107Pd for the early history of the solar system. Variations in 53Cr/52Cr and Mn/Cr ratios from several meteorites indicate an initial 53Mn/55Mn ratio that suggests Mn-Cr isotopic systematics must result from in-situ decay of 53Mn in differentiated planetary bodies. Hence 53Mn provides additional evidence for nucleosynthetic processes immediately before coalescence of the solar system.
   The isotopes of manganese range in atomic weight from 46 u (46Mn) to 65 u (65Mn). The primary decay mode before the most abundant stable isotope, 55Mn, is electron capture and the primary mode after is beta decay.

Precautions

Manganese compounds are less toxic than those of other widespread metals such as nickel and copper. Exposure to manganese dusts and fumes shouldn't exceed the ceiling value of 5 mg/m3 even for short periods because of its toxicity level. Manganese poses a particular risk for children due to its propensity to bind to CH-7 receptors. Manganese poisoning has been linked to impaired motor skills and cognitive disorders. Essentially, chronic exposure to manganese dust has caused miners to go mad.
   Acidic permanganate solutions will oxidize any organic material they come into contact with. The oxidation process can generate enough heat to ignite some organic substances.
   In 2005, a study suggested a possible link between manganese inhalation and central nervous system toxicity in rats. It is hypothesized that long-term exposure to the naturally occurring manganese in shower water puts up to 8.7 million Americans at risk.
   A form of neurodegeneration similar to Parkinson's Disease called "manganism" has been linked to manganese exposure amongst miners and smelters since the early 19th Century. Allegations of inhalation-induced manganism have been made regarding the welding industry. Manganese exposure USA is regulated by Occupational Safety and Health Administration.

Further Information

Get more info on 'Manganese'.


External Link Exchanges

Do you know how hard it is to get a link from a large encyclopaedia? Well we're different and will prove it. To get a link from us just add the following HTML to your site on a relevant page:

    <a href="http://manganese.totallyexplained.com">Manganese Totally Explained</a>

Then simply click through this link from your web page. Our crawlers will verify your link, extract the title of your web page and instantly add a link back to it. If you like you can remove the words Totally Explained and embed the link in article text.
   As long as your link remains in place, we'll keep our link to you right here. Please play fair - our crawlers are watching. Your site must be closely related to this one's topic. Any kind of spamming, dubious practises or removing the link will result in your link from us being dropped and, potentially, your whole site being banned.



Copyright © 2007-8 totallyexplained.com | Licensed under the GNU Free Documentation License | Site Map
This article contains text from the Wikipedia article Manganese (History) and is released under the GFDL | RSS Version