Iron(III) sulfate

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Iron(III) sulfate
Siran zelezity.JPG
Names
IUPAC name
Iron(III) sulfate
Other names
Ferric sulfate
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.030.054 OOjs UI icon edit-ltr-progressive.svg
PubChem CID
RTECS number
  • NO8505000
UNII
  • InChI=1S/2Fe.3H2O4S/c;;3*1-5(2,3)4/h;;3*(H2,1,2,3,4)/q2*+3;;;/p-6 Yes check.svgY
    Key: RUTXIHLAWFEWGM-UHFFFAOYSA-H Yes check.svgY
  • InChI=1/2Fe.3H2O4S/c;;3*1-5(2,3)4/h;;3*(H2,1,2,3,4)/q2*+3;;;/p-6
    Key: RUTXIHLAWFEWGM-CYFPFDDLAR
  • [Fe+3].[Fe+3].[O-]S(=O)(=O)[O-].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O
Properties
Fe2(SO4)3
Molar mass 399.88 g/mol (anhydrous)
489.96 g/mol (pentahydrate)
562.00 g/mol (nonahydrate)
Appearancegrayish-white crystals
Density 3.097 g/cm3 (anhydrous)
1.898 g/cm3 (pentahydrate)
Melting point 480 °C (896 °F; 753 K) (anhydrous)(decomposes)
175 °C (347 °F) (nonahydrate)
256g/L (monohydrate, 293K)
Solubility sparingly soluble in alcohol
negligible in acetone, ethyl acetate
insoluble in sulfuric acid, ammonia
1.814 (anhydrous)
1.552 (nonahydrate)
Hazards
NFPA 704 (fire diamond)
NFPA 704.svgHealth 1: Exposure would cause irritation but only minor residual injury. E.g. turpentineFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
1
0
0
Lethal dose or concentration (LD, LC):
500 mg/kg (oral, rat)
NIOSH (US health exposure limits):
REL (Recommended)
TWA 1 mg/m3 [1]
Related compounds
Other anions
Iron(III) chloride
Iron(III) nitrate
Related compounds
Iron(II) sulfate
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
X mark.svgN  verify  (what is  Yes check.svgYX mark.svgN ?)

Iron(III) sulfate (or ferric sulfate), is a family of inorganic compounds with the formula Fe2(SO4)3(H2O)n. A variety of hydrates are known, including the most commonly encountered form of "ferric sulfate". Solutions are used in dyeing as a mordant, and as a coagulant for industrial wastes. Solutions of ferric sulfate are also used in the processing of aluminum and steel. [2] [3]

Contents

Speciation

The various crystalline forms of Fe2(SO4)3(H2O)n are well-defined, often by X-ray crystallography. The nature of the aqueous solutions is often less certain, but aquo-hydroxo complexes such as [Fe(H2O)6]3+ and [Fe(H2O)5(OH)]2+ are often assumed. [4] Regardless, all such solids and solutions feature ferric ions, each with five unpaired electrons. By virtue of this high spin d5 electronic configuration, these ions are paramagnetic and are weak chromophores.

Production

Ferric sulfate solutions are usually generated from iron wastes. The actual identity of the iron species is often vague, but many applications do not demand high purity materials. It is produced on a large scale by treating sulfuric acid, a hot solution of ferrous sulfate, and an oxidizing agent. Typical oxidizing agents include chlorine, nitric acid, and hydrogen peroxide. [5]

2 FeSO4 + H2SO4 + H2O2 → Fe2(SO4)3 + 2 H2O

Natural occurrences

Iron sulfates occur as a variety of rare (commercially unimportant) minerals. Mikasaite, a mixed iron-aluminium sulfate of chemical formula (Fe3+, Al3+)2(SO4)3 [6] is the name of mineralogical form of iron(III) sulfate. This anhydrous form occurs very rarely and is connected with coal fires. The hydrates are more common, with coquimbite [7] (nonahydrate) as probably the most often met among them. Paracoquimbite is the other, rarely encountered natural nonahydrate. Kornelite (heptahydrate) and quenstedtite (decahydrate) are rarely found. Andradite garnet is a yellow-green example found in Italy. [8] Lausenite (hexa- or pentahydrate) is a doubtful species. All the mentioned natural hydrates are unstable connected with the weathering (aerobic oxidation) of Fe-bearing primary minerals (mainly pyrite and marcasite).

Coquimbite crystal structure Coquimbite crystal structure.png
Coquimbite crystal structure

See also

Related Research Articles

<span class="mw-page-title-main">Sulfuric acid</span> Chemical compound (H₂SO₄)

Sulfuric acid or sulphuric acid, known in antiquity as oil of vitriol, is a mineral acid composed of the elements sulfur, oxygen, and hydrogen, with the molecular formula H2SO4. It is a colorless, odorless, and viscous liquid that is miscible with water.

<span class="mw-page-title-main">Ferrous</span> The element iron in its +2 oxidation state

In chemistry, iron(II) refers to the element iron in its +2 oxidation state. The adjective ferrous or the prefix ferro- is often used to specify such compounds, as in ferrous chloride for iron(II) chloride (FeCl2). The adjective ferric is used instead for iron(III) salts, containing the cation Fe3+. The word ferrous is derived from the Latin word ferrum, meaning "iron".

<span class="mw-page-title-main">Iron(II) sulfate</span> Chemical compound

Iron(II) sulfate (British English: iron(II) sulphate) or ferrous sulfate denotes a range of salts with the formula FeSO4·xH2O. These compounds exist most commonly as the heptahydrate (x = 7) but several values for x are known. The hydrated form is used medically to treat or prevent iron deficiency, and also for industrial applications. Known since ancient times as copperas and as green vitriol (vitriol is an archaic name for sulfate), the blue-green heptahydrate (hydrate with 7 molecules of water) is the most common form of this material. All the iron(II) sulfates dissolve in water to give the same aquo complex [Fe(H2O)6]2+, which has octahedral molecular geometry and is paramagnetic. The name copperas dates from times when the copper(II) sulfate was known as blue copperas, and perhaps in analogy, iron(II) and zinc sulfate were known respectively as green and white copperas.

Sulfide (British English also sulphide) is an inorganic anion of sulfur with the chemical formula S2− or a compound containing one or more S2− ions. Solutions of sulfide salts are corrosive. Sulfide also refers to large families of inorganic and organic compounds, e.g. lead sulfide and dimethyl sulfide. Hydrogen sulfide (H2S) and bisulfide (SH) are the conjugate acids of sulfide.

Iron(III) chloride describes the inorganic compounds with the formula FeCl3(H2O)x. Also called ferric chloride, these compounds are some of the most important and commonplace compounds of iron. They are available both in anhydrous and in hydrated forms which are both hygroscopic. They feature iron in its +3 oxidation state. The anhydrous derivative is a Lewis acid, while all forms are mild oxidizing agents. It is used as a water cleaner and as an etchant for metals.

<span class="mw-page-title-main">Zinc sulfate</span> Chemical compound

Zinc sulfate describes a family of inorganic compounds with the formula ZnSO4(H2O)x. All are colorless solids. The most common form includes water of crystallization as the heptahydrate, with the formula ZnSO4·7H2O. As early as the 16th century it was prepared on the large scale, and was historically known as "white vitriol" (the name was used, for example, in 1620s by the collective writing under the pseudonym of Basil Valentine). Zinc sulfate and its hydrates are colourless solids.

<span class="mw-page-title-main">Cerium(IV) sulfate</span> Chemical compound

Cerium(IV) sulfate, also called ceric sulfate, is an inorganic compound. It exists as the anhydrous salt Ce(SO4)2 as well as a few hydrated forms: Ce(SO4)2(H2O)x, with x equal to 4, 8, or 12. These salts are yellow to yellow/orange solids that are moderately soluble in water and dilute acids. Its neutral solutions slowly decompose, depositing the light yellow oxide CeO2. Solutions of ceric sulfate have a strong yellow color. The tetrahydrate loses water when heated to 180-200 °C.

In chemistry, water(s) of crystallization or water(s) of hydration are water molecules that are present inside crystals. Water is often incorporated in the formation of crystals from aqueous solutions. In some contexts, water of crystallization is the total mass of water in a substance at a given temperature and is mostly present in a definite (stoichiometric) ratio. Classically, "water of crystallization" refers to water that is found in the crystalline framework of a metal complex or a salt, which is not directly bonded to the metal cation.

Iron(II) chloride, also known as ferrous chloride, is the chemical compound of formula FeCl2. It is a paramagnetic solid with a high melting point. The compound is white, but typical samples are often off-white. FeCl2 crystallizes from water as the greenish tetrahydrate, which is the form that is most commonly encountered in commerce and the laboratory. There is also a dihydrate. The compound is highly soluble in water, giving pale green solutions.

<span class="mw-page-title-main">Iron(II) sulfide</span> Chemical compound

Iron(II) sulfide or ferrous sulfide is one of a family of chemical compounds and minerals with the approximate formula FeS. Iron sulfides are often iron-deficient non-stoichiometric. All are black, water-insoluble solids.

<span class="mw-page-title-main">Iron(II) hydroxide</span> Chemical compound

Iron(II) hydroxide or ferrous hydroxide is an inorganic compound with the formula Fe(OH)2. It is produced when iron(II) salts, from a compound such as iron(II) sulfate, are treated with hydroxide ions. Iron(II) hydroxide is a white solid, but even traces of oxygen impart a greenish tinge. The air-oxidised solid is sometimes known as "green rust".

<span class="mw-page-title-main">Double salt</span> Type of salt

A double salt is a salt that contains two or more different cations or anions. Examples of double salts include alums (with the general formula MIMIII(SO4)2·12H2O) and Tutton's salts (with the general formula (MI)2MII(SO4)2·6H2O). Other examples include potassium sodium tartrate, ammonium iron(II) sulfate (Mohr's salt), potassium uranyl sulfate (used to discover radioactivity) and bromlite BaCa(CO3)2. The fluorocarbonates contain fluoride and carbonate anions. Many coordination complexes form double salts.

<span class="mw-page-title-main">Iron(III) nitrate</span> Chemical compound

Iron(III) nitrate, or ferric nitrate, is the name used for a series of inorganic compounds with the formula Fe(NO3)3.(H2O)n. Most common is the nonahydrate Fe(NO3)3.(H2O)9. The hydrates are all pale colored, water-soluble paramagnetic salts.

Iron shows the characteristic chemical properties of the transition metals, namely the ability to form variable oxidation states differing by steps of one and a very large coordination and organometallic chemistry: indeed, it was the discovery of an iron compound, ferrocene, that revolutionalized the latter field in the 1950s. Iron is sometimes considered as a prototype for the entire block of transition metals, due to its abundance and the immense role it has played in the technological progress of humanity. Its 26 electrons are arranged in the configuration [Ar]3d64s2, of which the 3d and 4s electrons are relatively close in energy, and thus it can lose a variable number of electrons and there is no clear point where further ionization becomes unprofitable.

<span class="mw-page-title-main">Ammonium iron(II) sulfate</span> Chemical compound

Ammonium iron(II) sulfate, or Mohr's salt, is the inorganic compound with the formula (NH4)2Fe(SO4)2(H2O)6. Containing two different cations, Fe2+ and NH+4, it is classified as a double salt of ferrous sulfate and ammonium sulfate. It is a common laboratory reagent because it is readily crystallized, and crystals resist oxidation by air. Like the other ferrous sulfate salts, ferrous ammonium sulfate dissolves in water to give the aquo complex [Fe(H2O)6]2+, which has octahedral molecular geometry. Its mineral form is mohrite.

Biomining ( phytomining) is the concept of extracting metals from ores and other solid materials typically using prokaryotes, fungi or plants (phytoextraction. These organisms secrete organic compounds that chelate metals from the environment. The proposed technology is often aimed at extraction of iron, copper, zinc, gold, uranium, and thorium. Large chemostats of microbes can be grown to leach metals from their media. If it were practical, biomining would be an environmentally friendly alternative to traditional mining.

<span class="mw-page-title-main">Chromium(III) sulfate</span> Chemical compound

Chromium(III) sulfate usually refers to the inorganic compounds with the formula Cr2(SO4)3.x(H2O), where x can range from 0 to 18. Additionally, ill-defined but commercially important "basic chromium sulfates" are known. These salts are usually either violet or green solids that are soluble in water. It is commonly used in tanning leather.

<span class="mw-page-title-main">Ammonium iron(III) sulfate</span> Chemical compound

Ammonium iron(III) sulfate, NH4Fe(SO4)2·12 H2O, or NH4[Fe(H2O)6](SO4)2·6 H2O, also known as ferric ammonium sulfate (FAS) or iron alum, is a double salt in the class of alums, which consists of compounds with the general formula AB(SO4)2 · 12 H2O. It has the appearance of weakly violet, octahedrical crystals. There has been some discussion regarding the origin of the crystals' color, with some ascribing it to impurities in the compound, and others claiming it to be a property of the crystal itself.

<span class="mw-page-title-main">Iron(II) citrate</span> Chemical compound

Ferrous citrate, also known as iron(II) citrate or iron(2+) citrate, describes coordination complexes containing citrate anions with Fe2+ formed in aqueous solution. Although a number of complexes are possible (or even likely), only one complex has been crystallized. That complex is the coordination polymer with the formula [Fe(H2O)6]2+{[Fe(C6H5O7)(H2O)]}2.2H2O, where C6H5O73- is HOC(CH2CO2)2(CO2, i.e., the triple conjugate base of citric acid wherein the three carboxylic acid groups are ionized. Ferrous citrates are all paramagnetic, reflecting the weak crystal field of the carboxylate ligands.

Iron(II) selenate (ferrous selenate) is an inorganic compound with the formula FeSeO4. It has anhydrous and several hydrate forms. The pentahydrate has the structure, [Fe(H2O)4]SeO4•H2O, isomorphous to the corresponding iron(II) sulfate. Heptahydrate is also known, in form of unstable green crystalline solid.

References

  1. NIOSH Pocket Guide to Chemical Hazards. "#0346". National Institute for Occupational Safety and Health (NIOSH).
  2. Ferric sulfate. The Columbia Encyclopedia, Sixth Edition. Retrieved November, 2007.
  3. Wildermuth, Egon; Stark, Hans; Friedrich, Gabriele; Ebenhöch, Franz Ludwig; Kühborth, Brigitte; Silver, Jack; Rituper, Rafael (2000). "Iron Compounds". Ullmann's Encyclopedia of Industrial Chemistry . Weinheim: Wiley-VCH. doi:10.1002/14356007.a14_591. ISBN   978-3527306732.
  4. Grant, M.; Jordan, R. B. (1981). "Kinetics of Solvent Water Exchange on Iron(III)". Inorganic Chemistry. 20: 55–60. doi:10.1021/ic50215a014.
  5. Iron compounds. Encyclopædia Britannica Article. Retrieved November, 2007
  6. Mikasaite
  7. "Minerals Colored by Metal Ions". minerals.gps.caltech.edu. Retrieved 2023-03-01.
  8. "Minerals Colored by Metal Ions". minerals.gps.caltech.edu. Retrieved 2023-03-01.