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Iron Basic information

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Iron Chemical Properties

Melting point:
1535 °C(lit.)
Boiling point:
2750 °C(lit.)
7.86 g/mL at 25 °C(lit.)
Flash point:
>230 °F
storage temp. 
H2O: soluble
Specific Gravity
9.71 μΩ-cm
Water Solubility 
Moisture Sensitive
Stable. Reacts slowly with moist air and water. Dust may form an explosive or combustible mixture with air. Incompatible with organic acids, strong oxidizing agents, water, mineral acids.
CAS DataBase Reference
7439-89-6(CAS DataBase Reference)
NIST Chemistry Reference
EPA Substance Registry System
Iron (7439-89-6)

Safety Information

Hazard Codes 
Risk Statements 
Safety Statements 
UN 3264 8/PG 3
WGK Germany 
HS Code 
Hazardous Substances Data
7439-89-6(Hazardous Substances Data)
LD50 oral in rat: 30gm/kg



Iron Usage And Synthesis


Iron has been known to mankind from early civilization. In fact, a period of history, the “iron age,” is named for the widespread use of this metal. For almost a thousand years, it remained as the single most-used metal, and its use in mechanization made the industrial revolution possible.
Iron, after oxygen, silicon and aluminum, is the fourth most abundant element in the earth’s crust. It is the prime constituent of earth’s core along with nickel. Its abundance in the crust is 5.63%. Its concentration in the seawater is about 0.002mg/L. The principal ores of iron are hematite, Fe2O3; pyrite, Fe2S2; ilmenite, FeTiO3; magnetite, Fe3O4; siderite, Fe2CO3; and limonite [FeO(OH)]. It also is found in a number of minerals, such as corundum, as an impurity. It also is found in meteorites.
Iron occurs in every mammalian cell and is vital for life processes. It is bound to various proteins and found in blood and tissues. The iron-porphyrin or heme proteins include hemoglobin, myoglobin and various heme enzymes, such as cytochromes and peroxidases. Also, it occurs in non heme compounds, such as ferritin, siderophilin, and hemosiderin. Hemoglobin, found in the red blood cells, is responsible for transport of oxygen to the tissue cells and constitutes about two-thirds (mass) of all iron present in the human body. An adult human may contain about 4 to 6 grams of iron.

Chemical properties

Gray metal; It should be dissolved in hydrochloric acid, sulfuric acid and dilute nitric acid.

Content analysis

Accurately weigh approximately 200 mg of the sample and transfer it into a 300 ml Erlenmeyer flask, add 50 ml of a dilute sulfuric acid solution (TS-241). Use a plug containing a Bunsen valve (the production method is to insert a glass tube connected with a short segment of rubber tube to the plug. The side of the rubber tube has a long slit while the other side is inserted of a glass rod so that the gas can escape and the air can’t enter). The solution was heated on a steam bath to dissolve the iron. After cooling, dilute with 50 ml of freshly boiled and cooled water. Add 2 drops of the test solution (TS-162) to 0.1 mol/L
Apply cerium sulfate titration to until the red color becomes light blue color. Each ml of 0.1mol/L of high cerium sulfate are equivalent to 5.585 mg of iron (Fe).
The method is the same as that of "reduced iron (01219)”.


Industrial uses of iron as carbon steels are numerous and surpass any 410 IRONother alloys. Carbon steels are alloys of iron containing carbon in varying proportions, usually up to 1.7% carbon. Other metals also are incorporated into carbon steels to produce low-alloy steels. Such metals are usually nickel and chromium and are classified as stainless steel, tool steels, and heat-resistant steels. Non-steel iron alloys such as cast iron, wrought iron, nickel iron and silicon iron also have many important applications. Another important application of iron is as an industrial catalyst. It is used in catalyst compositions in the Haber process for synthesis of ammonia, and in Fischer-Tropsch process for producing synthetic gasoline.The followings are some examples of common applications:

  • pharmaceuticals, pesticides, powder metallurgy and so on;
  • as a hot hydrogen generator, gel propellant, combustion activator, catalyst, water cleaning adsorbent, sintered active agent, etc;used for powder metallurgy products, all kinds of mechanical parts and components products, cemented carbide products, etc;
  • as a reducing agent as well as being used for iron salt manufacturing and electronics industry;
  • as nutritional supplements (iron fortifier),for casting,or as reducing agent;
  • in the electronics industry, powder metallurgy.

Production Methods

Most iron produced today is from its oxide minerals, hematite and magnetite. The process involves reducing mineral iron with carbon in a blast furIRON 411nace. There are several types of blast furnaces which vary in design and dimensions. The overall processes, however, are more or less the same. One such process is outlined below:
The mixture of ore, coke and limestone is fed into the blast furnace from the top. The materials are preheated to about 200°C in the top most zone. Hematite is partially reduced to magnetite and then to FeO by the ascending stream of carbon monoxide formed at the bottom and mid zones of the furnace resulting from high temperature oxidation of carbon. The ferrous oxide FeO formed at the top zone is reduced to metallic iron at about 700°C in the mid zone by carbon monoxide. A hot air blast at 900°C passes through the entire furnace for a very short time (usually for a few seconds). This prevents any gassolid reaction product from reaching equilibrium. In the temperature zone 700 to 1,200°C ferrous oxide is completely reduced to iron metal by carbon monoxide. Also, more CO is formed by oxidation of carbon by carbon dioxide. Further down the furnace at higher temperatures, around 1,500°C, iron melts, dripping down into the bottom. Also, in this temperature zone acidic silica particles react with basic calcium oxide produced from the decomposition of limestone, producing calcium silicate. The molten waste calcium silicate also drips down into the bottom. In the hottest zone of the blast furnace, between 1,500 to 2,000°C, some carbon dissolves into the molten iron. Also at these temperatures any remaining silicates and phosphates are reduced to silicon and phosphorus, and dissolve into the molten iron. Additionally, other tract metals such as manganese dissolve into the molten iron. The impure iron melt containing about 3 to 4% carbon is called “pig iron”. At the bottom, the molten waste slag floats over the impure pig iron melt that is heavier than the slag melt and immiscible with it. Pig iron is separated from the slag and purified for making different types of steel. Chemical reactions and processes occurring in various temperature zones of blast furnace are summarized below:  production method   Pig iron produced in the blast furnace is purified and converted to steel in a separate furnace, known as a basic-oxygen furnace. Jets of pure oxygen gas at high pressure are blown over and through the pig iron melt. Metal impurities are converted into oxides. Part of the dissolved carbon in the impure iron melt is converted into carbon dioxide gas. Formation of SiO2, CO2, and other metal oxides are exothermic reactions that raise the temperature to sustain the melt. A lime flux (CaO) also is added into the melt, which converts silica into calcium silicate, CaSiO3, and phosphorus into calcium phosphate, Ca3(PO4)2, forming a molten slag immiscible with molten steel. The lighter molten slag is decanted from the heavier molten steel.  


China pyrrhotite-type sulfur pyrite mine has less of mining hills resources. Take the MinXi mine in the DaTian City, Fujian Province and Zhangjiagou mine in Dandong City, Liaoning Province as the representatives; both of them are underground mining mines. The former applies the Housing pile mining method while the later one uses the section mining method. The pit mining process is the same as the method of "phosphate rock." Beneficiation methods include flotation process and flotation-magnetic combined process.


Iron Powder: GRAS (FDA, § 184.1375, 2000); Inhalation of dust can cause pneumoconiosis. Operation personnel should wear overall, wear dust masks and other labor insurance products. Production equipment should be closed, the workshop should be well-ventilated. Be sure to pay attention to dust protection.


Carbonyl iron is elemental iron produced by the decomposition of iron pentacarbonyl as a dark gray powder. When viewed under a microscope having a magnifying power of 500 diameters or greater, it appears as spheres built up with concentric shells. It is stable in dry air.


Reduced iron is elemental iron obtained by a chemical process in the form of a grayish black powder, all of which should pass through a 100-mesh sieve. It is lusterless or has not more than a slight luster. When viewed under a microscope having a magnifying power of 100 diameters, it appears as an amorphous powder, free from particles having a crystalline structure. It is stable in dry air.

Chemical Properties

Silver-white malleable metal. The only metal that can be tempered. Mechanical properties are altered by impurities, especially carbon.Iron is highly reactive chemically, a strong reducing agent, oxidizes readily in moist air, reacts with steam when hot, t

Physical properties

Pure iron is a silvery-white, hard, but malleable and ductile metal that can be worked andforged into many different shapes, such as rods, wires, sheets, ingots, pipes, framing, and soon. Pure iron is reactive and forms many compounds with other elements. It is an excellentreducing agent. It oxidizes (rusts) in water and moist air and is highly reactive with most acids,releasing hydrogen from the acid. One of its main properties is that it can be magnetized andretain a magnetic field.The iron with a valence of 2 is referred to as “ferrous” in compounds (e.g., ferrous chloride= FeCl2). When the valence is 3, it is called “ferric” (e.g., ferric chloride = FeCl3).Iron’s melting point is 1,535°C, its boiling point is 2,750°C, and its density is 7.873g/cm3.


There are 30 isotopes of iron ranging from Fe-45 to Fe-72. The following arethe four stable isotopes with the percentage of their contribution to the element’s naturalexistence on Earth: Fe-54 = 5.845%, Fe-56 = 91.72%, Fe-57 = 2.2%, and Fe-58 =0.28%. It might be noted that Fe-54 is radioactive but is considered stable because ithas such a long half-life (3.1×10+22 years). The other isotopes are radioactive and areproduced artificially. Their half-lives range from 150 nanoseconds to 1×105 years.

Origin of Name

The name “iron” or “iren” is Anglo-Saxon, and the symbol for iron (Fe) is from ferrum, the Latin word for iron.


Iron is the fourth most abundant element in the Earth s crust (about 5%) and is the ninth most abundant element found in the sun and stars in the universe. The core of the Earth is believed to consist of two layers, or spheres, of iron. The inner core is thought to be molten iron and nickel mixture, and the outer core is a transition phase of iron with the molten magma of the Earth s mantle. Iron s two oxide compounds (ferrous(II) oxide FeO) and (ferric(III) oxide Fe2O3) are the third and seventh most abundant compounds found in the Earth s crust. The most common ore of iron is hematite that appears as black sand on beaches or black seams when exposed in the ground. Small amounts of iron and iron alloys with nickel and cobalt were found in meteorites (siderite) by early humans. This limited supply was used to shape tools and crude weapons. Even though small amounts of iron compounds and alloys are found in nature (iron is not found in its pure metallic state in nature), early humans did not know how to extract iron from ores until well after they knew how to smelt gold, tin, and copper ores. From these metals, they then developed bronze alloy thus the Bronze Age (about 8000 BCE). There are several grades of iron ores, including hematite (brown ferric oxide) and limonite (red ferric oxide). Other ores are pyrites, chromite, magnetite, siderite, and low-grade taconite. Magnetite (Fe3O4) is the magnetic iron mineral/ore found in South Africa, Sweden, and parts of the United States. The lodestone, a form of magnetite, is a natural magnet. Iron ores are found in many countries. Iron is found throughout most of the universe, in most of the stars, and in our sun, and it probably exists on the other planets of our solar system.


Iron is the only metal that can be tempered (hardened by heating, then quenching in wateror oil). Iron can become too hard and develop stresses and fractures. This can be corrected byannealing, a process that heats the iron again and then holds it at that temperature until thestresses are eliminated. Iron is a good conductor of electricity and heat. It is easily magnetized,but its magnetic properties are lost at high temperatures. Iron has four allotropic states. Thealpha form exists at room temperatures, while the other three allotropic forms exist at varyinghigher temperatures.Iron is the most important construction metal. It can be alloyed with many other metals tomake a great variety of specialty products. Its most important alloy is steel.An interesting characteristic of iron is that it is the heaviest element that can be formed byfusion of hydrogen in the sun and similar stars. Hydrogen nuclei can be “squeezed” in the sunto form all the elements with atomic numbers below cobalt (27Co), which includes iron. Itrequires the excess fusion energy of supernovas (exploding stars) to form elements with protonnumbers greater than iron (26Fe).


Iron is a relatively abundant element in the universe. It is found in the sun and many types of stars in considerable quantity. It has been suggested that the iron we have here on Earth may have originated in a supernova. Iron is a very difficult element to produce in ordinary nuclear reactions, such as would take place in the sun. Iron is found native as a principal component of a class of iron–nickel meteorites known as siderites, and is a minor constituent of the other two classes of meteorites. The core of the Earth, 2150 miles in radius, is thought to be largely composed of iron with about 10% occluded hydrogen. The metal is the fourth most abundant element, by weight, making up the crust of the Earth. The most common ore is hematite (Fe2O3). Magnetite (Fe3O4) is frequently seen as black sands along beaches and banks of streams. Lodestone is another form of magnetite. Taconite is becoming increasingly important as a commercial ore. Iron is a vital constituent of plant and animal life, and appears in hemoglobin. The pure metal is not often encountered in commerce, but is usually alloyed with carbon or other metals. The pure metal is very reactive chemically, and rapidly corrodes, especially in moist air or at elevated temperatures. It has four allotropic forms,or ferrites, known as α, β, γ, and δ, with transition points at 700, 928, and 1530°C. The α form is magnetic, but when transformed into the β form, the magnetism disappears although the lattice remains unchanged. The relations of these forms are peculiar. Pig iron is an alloy containing about 3% carbon with varying amounts of S, Si, Mn, and P. It is hard, brittle, fairly fusible, and is used to produce other alloys, including steel. Wrought iron contains only a few tenths of a percent of carbon, is tough, malleable, less fusible, and usually has a “fibrous” structure. Carbon steel is an alloy of iron with carbon, with small amounts of Mn, S, P, and Si. Alloy steels are carbon steels with other additives such as nickel, chromium, vanadium, etc. Iron is the cheapest and most abundant, useful, and important of all metals. Natural iron contains four isotopes. Twenty-six other isotopes and isomers, all radioactive, are now recognized.


Alloyed with C, Mn, Cr, Ni, and other elements to form steels. Nutritional supplement in wheat flours, corn meal, grits and other cereal products. 55Fe and 59Fe used in tracer studies; the former in biological studies.


Smelting of iron from its ore occurs in a blast furnace where carbon (coke) and limestoneare heated with the ore that results in the iron in the ore being reduced and converted tomolten iron, called “pig iron.” Melted pig iron still contains some carbon and silicon as wellas some other impurities as it collects in the bottom of the furnace with molten slag floatingatop the iron. Both are tapped and drained off. This process can be continuous since moreingredients can be added as the iron and slag are removed from the bottom of the furnace.This form of iron is not very useful for manufacturing products, given that it is brittle andnot very strong.One of the major advances in the technology of iron smelting was the development of theBessemer process by Henry Bessemer (1813–1898). In this process, compressed air or oxygenis forced through molten pig iron to oxidize (burn out) the carbon and other impurities. Steelis then produced in a forced oxygen furnace, where carbon is dissolved in the iron at very hightemperatures. Variations of hardness and other characteristics of steel can be achieved with theaddition of alloys and by annealing, quench hardening, and tempering the steel.Powder metallurgy (sintering) is the process whereby powdered iron or other metals arecombined together at high pressure without high heat to fit molded forms. This process is usedto produce homogenous (uniform throughout) metal parts.One of the most useful characteristics of iron is its natural magnetism, which it loses athigh temperatures. Magnetism can also be introduced into iron products by electrical induction. Magnets of all sizes and shapes are used in motors, atom smashers, CT scanners, and TV and computer screens, toname a few uses. Super magnets can be formed by addingother elements (see cobalt) tohigh-quality iron.Iron is an important element making up hemoglobinin the blood, which carriesoxygen to the cells of ourbodies. It is also very important as a trace element inthe diet, assisting with theoxidation of foods to produce energy. We need about10 to 18 milligrams of ironeach day, as a trace mineral.Iron is found in liver andmeat products, eggs, shellfish, green leafy vegetables,peas, beans, and whole graincereals. Iron deficiency maycause anemia (low red bloodcell count), weakness, fatigue,headaches, and shortness ofbreath. Excess iron in thediet can cause liver damage,but this is a rare condition.


Iron is a mineral used in food fortification that is necessary for the prevention of anemia, which reduces the hemoglobin concentra- tion and thus the amount of oxygen delivered to the tissues. sources include ferric ammonium sulfate, chloride, fructose, glycerophos- phate, nitrate, phosphate, pyrophosphate and ferrous ammonium sulfate, citrate, sulfate, and sodium iron edta. the ferric form (fe3+) is iron in the highest valence state and the ferrous form (fe2+) is iron in a lower valence state. the iron source should not discolor or add taste and should be stable. iron powders produce low discoloration and rancidity. it is used for fortification in flour, baked goods, pasta, and cereal products.


iron: Symbol Fe. A silvery malleableand ductile metallic transition element;a.n. 26; r.a.m. 55.847; r.d.7.87; m.p. 1535°C; b.p. 2750°C. Themain sources are the ores haematite(Fe2O3), magnetite (Fe3O4), limonite(FeO(OH)nH2O), ilmenite (FeTiO3),siderite (FeCO3), and pyrite (FeS2).The metal is smelted in a blast furnaceto give impure pig iron, whichis further processed to give castiron, wrought iron, and varioustypes of steel. The pure element hasthree crystal forms: alpha-iron, stablebelow 906°C with a body-centredcubicstructure; gamma-iron, stablebetween 906°C and 1403°C with anonmagnetic face-centred-cubicstructure; and delta-iron, which isthe body-centred-cubic form above1403°C. Alpha-iron is ferromagneticup to its Curie point (768°C). The elementhas nine isotopes (mass numbers52–60), and is the fourth mostabundant in the earth’s crust. It is requiredas a trace element (see essentialelement) by living organisms.Iron is quite reactive, being oxidizedby moist air, displacing hydrogenfrom dilute acids, and combiningwith nonmetallic elements. It formsionic salts and numerous complexeswith the metal in the +2 or +3 oxidationstates. Iron(VI) also exists in theferrate ion FeO42-, and the elementalso forms complexes in which its oxidationnumber is zero (e.g. Fe(CO)5).


Wrought iron is a highly refinedform of iron containing 1–3% of slag(mostly iron silicate), which is evenlydistributed throughout the materialin threads and fibres so that the producthas a fibrous structure quite dissimilarto that of crystalline cast iron.Wrought iron rusts less readily thanother forms of metallic iron and itwelds and works more easily. It isused for chains, hooks, tubes, etc.


Metallic element of atomic number 26, group VIII of the periodic table, aw 55.847, valences = 2,3; four stable isotopes, 4 artificially radioactive isotopes.

Production Methods

Iron ore reserves are found worldwide. Areas with more than 1 billion metric tons of reserves include Australia, China, Brazil, Canada, the United States, Venezuela, South Africa, India, the former Soviet Union, Gabon, France, Spain, Sweden, and Algeria. The ore exists in varying grades, ranging from 20 to 70% iron content. North America has been fortunate in its ore deposits. There are commercially usable quantities in 22 U.S. states and in six Canadian provinces. In the United States the most abundant supplies, discovered in the early 1890s, are located in the Lake Superior region around the Mesabi Range. Other large deposits are found in Alabama, Utah, Texas, California, Pennsylvania, and New York. These deposits, particularly the Mesabi Range reserves, seemed inexhaustible in the 1930s when an average of 30 million tons of ore was produced annually from that one range. The tremendous demand for iron ore duringWorldWar II virtually tripled the output of the Mesabi Range and severely depleted its deposits of high-grade ore. The major domestic (U.S.) production is nowfrom crude iron ore, mainly taconite, a low-grade ore composed chiefly of hematite [FeO(OH) ·H2O] and silica found in the Great Lakes region.

General Description

A gray lustrous powder. Used in powder metallurgy and as a catalyst in chemical manufacture.

Air & Water Reactions

Highly flammable. May react with water to give off hydrogen, a flammable gas. The heat from this reaction may ignite the hydrogen.

Reactivity Profile

Iron is pyrophoric [Bretherick, 1979 p. 170-1]. A strong reducing agent and therefore incompatible with oxidizing agents. Burns in chlorine gas [Mellor 2, Supp. 1:380 1956]. Reacts with fluorine with incandescence [Mellor 13:314, 315, 1946-1947].


Iron dust from most iron compounds is harmful if inhaled and toxic if ingested. Iron dustand powder (even filings) are flammable and can explode if exposed to an open flame. Asmentioned, excessive iron in the diet may cause liver damage.

Health Hazard

Fire may produce irritating and/or toxic gases. Contact may cause burns to skin and eyes. Contact with molten substance may cause severe burns to skin and eyes. Runoff from fire control may cause pollution.

Fire Hazard

Flammable/combustible material. May be ignited by friction, heat, sparks or flames. Some may burn rapidly with flare burning effect. Powders, dusts, shavings, borings, turnings or cuttings may explode or burn with explosive violence. Substance may be transported in a molten form at a temperature that may be above its flash point. May re-ignite after fire is extinguished.

Agricultural Uses

Among the common and familiar metals, iron (Fe) is one of the essential plant nutrient elements. It has the atomic number of 26 and belongs to Group 8 of the Periodic Table
Iron is required in plants at the rate of 50to 250ppm and is, therefore, a micronutrient. It is mainly involved in biochemical processes which are mostly enzymatic oxidation-reduction reactions. In these reactions electrons are transferred from an electron donor to an electron acceptor.
Iron is also involved in respiration and photosynthesis. Some of the enzymatic involvements of iron are in (a) nitrate reductase activity, (b) reducing cytochrome-C by flavin enzyme, and (c) a protein (derived from iron ferridoxin) participating in photosynthetic electron transport.
Iron is a structural component of porphyrin molecules like cytochromes, hemes, hematin, ferritin, ferrichrome and leghemoglobin. The heme in hemoglobin is also a porphyrin derivative. Physiological processes of plants have shown that chlorophyll is formed from protoporphyrin by removing iron from hemin, whereas in other organisms, iron is introduced into protoporphyrin to form heme.
Iron is necessary for chlorophyll synthesis in plants. As much as 75% of cellular iron is associated with chloroplasts. Iron, which can replace molybdenum, is absorbed by the plant roots as ferrous ions or as complex organic salts and is absorbed by the leaves when applied as foliar sprays. It takes part in the plant’s oxidation- reduction reactions and activates several enzyme systems such as fumaric hydrogenase, catalase and oxydase.
Iron oxide is one of the least soluble minerals in aerated soils. In highly weathered soils, like oxisols and some ultisols, soluble materials leach out whereas the resistant hydrous iron oxides remain. Some oxisols contain up to 80% iron hydrous oxides as clay. Iron is not very soluble in soil solutions or water and, therefore, does not become easily available to plants. In strongly acidic solutions, however, iron is increasingly solubilized and becomes available to plants. In anaerobic conditions, ferrous iron is formed which is more soluble than ferric iron. Therefore, in the iron cycle, iron solubilizes in aerobic conditions and precipitates in anaerobic conditions.
Although soluble mineral iron is barely sufficient in soil, most plants get enough iron through decomposition of organic substances (like humic materials), exudative products from the root and microbial cells, animal manures and polyphenols extracted from leaf surfaces. These react and bind with iron, and facilitate iron solubility, making it more mobile in the form of solution.
The soil type, its characteristics, the nature of extractants used and the agro-ecological conditions dictate the availability of iron. The amount of iron in soils varies from as low as 200ppm to more than 10% as oxides, hydroxides, phosphates or silicates. In Indian soils, for instance, the available iron varies from traces to 386 ppm. The soil iron is progressively depleted by such factors as (a) intensive cultivation (with and without high yielding varieties), (b) adverse nutrient interaction, and (c) a decreased use of animal manures.
When the iron content falls below 50ppm, plants exhibit iron deficiency. This results in interveinal cldomsis (green vein color and yellow interveinal areas) in young leaves, which spreads rapidly to all the green foliage In severe iron deficiency, the leaves turn completely white. Fruit trees, ornamentals and grain sorghum show comparatively stronger symptoms than other crops.
In calcareous soils, the deficiency disease is called chlomis. Acid forming fertilizers used on such soils overcome iron deficiency. Soluble salts of iron added to soils get converted to insoluble hydroxides, oxides and phosphates, and do not assist in correcting iron deficiency. Some other causes for chlorosis are (a) imbalance of the metal ions such as copper and manganese, (b) excess of phosphorus in soils, and (c) a high pH level, lime content, soil moisture, bicarbonate in the rooting medium and cool temperatures.
in alkaline soils, iron forms insoluble salts like phosphates, whereas in acid soils iron salts are soluble, thus becoming available to plants.
In waterlogged soils, oxygen is depleted and ferric compounds are reduced to a more soluble ferrous form. The presence of organic matter in the soil also assists in creating a reducing environment which allows a periodic increase in the ferrous content of the soil. The longer the period of submergence in water, the greater the amount of ferrous iron formed. More than 300ppm of iron is toxic and causes nutritional disorders such as bronzing in rice, which is predominant when rice is grown in a poorly drained submerged soil.
Prolonged spray applications of Cu, Mn or Zn salts on poorly buffered soils can cause iron deficiency; the main cause being dilution of iron with respect to other metals (Cu, Zn, Mn). The iron deficiency in plants can be corrected by applying iron compounds (except ferrous sulphate which is not very effective as it gets oxidized to a ferric form) to the soil or by spraying aqueous salts on leaves. Alternatively, foliar sprays or direct injections of iron salts into the trunks and limbs of plants (iron medicaps) are found to be effective in controlling iron chlorosis. A ferrous sulphate aqueous solution of 4 to 6% at the rate of 30to 50g/acre in the spray can control chlorosis. The remedial chemicals most widely used to control chlorosis are iron chelates containing 6 to 12% iron. For instance, ferrous oxalate, though expensive, is used in the overall improvement of crops, as the quantity required is small.
Soluble iron compounds, diluted in water, are good for soil applications and spraying on foliage. Basic slag, (a by-product of the steel industry, which has oxides of phosphorus, calcium and magnesium as principal constituents) as well as soluble oxides of iron and manganese in small amounts, have a good effect on soil when added directly, in quantities of 560to 1,120kg/ha. Ferrous sulphate (FeSO4?7H2O), a by-product of the steel industry contains 19% Fe and is the most commonly used iron salt in plant nutrition. In an experiment, when 802 kg/ha of it was used on alkaline soils, it increased rice yield from 4,530to 6,042 kg/ha. NPK fertilizers contain iron in the range of 23 ppm to 1.19%. Many chelated products are also available as fertilizers. The iron deficiency can be improved by the addition of organic matter to well-drained soils. The improvement may be due to a better aeration and acceleration of iron reduction from the ferric to the ferrous form.

Purification Methods

Clean it in conc HCl, rinse in de-ionised water, then reagent grade acetone and dry it under vacuum.



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