Mohr's_salt

Ammonium iron(II) sulfate

Ammonium iron(II) sulfate

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.[1] Its mineral form is mohrite.

Quick Facts Names, Identifiers ...

Structure

This compound is a member of a group of double sulfates called Schönites or Tutton's salts. Tutton's salts form monoclinic crystals and have formula M2N(SO4)2·6H2O (M = various monocations). With regards to the bonding, crystals consist of octahedra [Fe(H2O)6]2+ centers, which are hydrogen bonded to sulfate and ammonium.[2]

Structure of ferrous ammonium sulfate with hydrogen bonding network highlighted (N is violet, O is red; S is orange, Fe = large red).

Mohr's salt is named after the German chemist Karl Friedrich Mohr, who made many important advances in the methodology of titration in the 19th century.

Applications

In analytical chemistry, this salt is the preferred source of ferrous ions as the solid has a long shelf life, being resistant to oxidation. This stability extends somewhat to solutions reflecting the effect of pH on the ferrous–ferric redox couple. This oxidation occurs more readily at high pH. The ammonium ions make solutions of Mohr's salt slightly acidic, which slows this oxidation process.[1][3] Sulfuric acid is commonly added to solutions to reduce oxidation to ferric iron.

It is used in the Fricke's dosimeter to measure high doses of gamma rays.[4]

Preparation

Mohr's salt forms upon evaporation of an equimolar mixture of aqueous ferrous sulfate and ammonium sulfate.[5]

Contaminants

Common impurities include magnesium, nickel, manganese, lead, and zinc, many of which form isomorphous salts.[6]


References

  1. Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  2. Ephraim, Fritz (1926). Inorganic Chemistry. tr P. C. L. Thorne. London: Gurney and Jackson. pp. 484–485.
  3. Hickman, C.; Lorrain, S.; Barthe, J.R.; Portal, G. (1986). "Use of Mohr's Salt for High Level Gamma Dosimetry (Up to 108 Gy)". Radiation Protection Dosimetry. 17 (1–4). Oxford Journals: 255–257. doi:10.1093/oxfordjournals.rpd.a079818.
  4. Wildermuth, Egon; Stark, Hans; Friedrich, Gabriele; Ebenhöch, Franz Ludwig; Kühborth, Brigitte; Silver, Jack; Rituper, Rafael (2000). "Iron Compounds". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a14_591. ISBN 978-3-527-30385-4.
  5. Vogel, Arthur I. (1961). A Text-book of Quantitative Inorganic Analysis Including Elementary Instrumental Analysis (3 ed.). Longmans. pp. 281–282.

Share this article:

This article uses material from the Wikipedia article Mohr's_salt, and is written by contributors. Text is available under a CC BY-SA 4.0 International License; additional terms may apply. Images, videos and audio are available under their respective licenses.