Jump to content

Potassium ferrocyanide

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Smokefoot (talk | contribs) at 02:27, 13 February 2016 (no mp or bp, per Talk). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Potassium ferrocyanide
Potassium ferrocyanide trihydrate
Names
IUPAC name
Potassium hexacyanoferrate(II)
Other names
(Yellow) Prussiate of Potash,[1]
Potassium hexacyanoferrate (II) trihydrate,
Tetrapotassium ferrocyanide trihydrate,
Ferrate hexacyano tetrapotassium trihydrate[2]
Identifiers
ECHA InfoCard 100.034.279 Edit this at Wikidata
E number E536 (acidity regulators, ...)
Properties
K4[Fe(CN)6]
Molar mass 368.35 g/mol (anhydrous)
422.388 g/mol (trihydrate)
Appearance Light yellow, crystalline granules
Density 1.85 g/cm3 (trihydrate)
Boiling point (decomposes)
trihydrate
28.9 g/100 mL (20 °C)
Solubility insoluble in ethanol, ether
Hazards
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 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
Flash point Non-flammable
Lethal dose or concentration (LD, LC):
6400 mg/kg (oral, rat)[3]
Related compounds
Other anions
Potassium ferricyanide
Other cations
Sodium ferrocyanide
Prussian blue
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Potassium ferrocyanide is the inorganic compound with formula K4[Fe(CN)6] · 3H2O. It is the potassium salt of the coordination complex [Fe(CN)6]4−. This salt forms lemon-yellow monoclinic crystals.

Synthesis

Modern production

Potassium ferrocyanide is produced industrially from hydrogen cyanide, ferrous chloride, and calcium hydroxide, the combination of which affords Ca2[Fe(CN)6] · 11H2O. This solution is then treated with potassium salts to precipitate the mixed calcium-potassium salt CaK2[Fe(CN)6], which in turn is treated with potassium carbonate to give the tetrapotassium salt.[4]

Historical production

Historically, the compound was manufactured from organically derived nitrogenous carbon sources, iron filings, and potassium carbonate.[5] Common nitrogen and carbon sources were torrified horn, leather scrap, offal, or dried blood.

Chemical reactions

Treatment of potassium ferrocyanide with nitric acid gives H2[Fe(NO)(CN)5]. After neutralization of this intermediate with sodium carbonate, red crystals of sodium nitroprusside can be selectively crystallized.[6]

Upon treatment with chlorine gas, potassium ferrocyanide converts to potassium ferricyanide:

2 K4[Fe(CN)6] + Cl2 → 2 K3[Fe(CN)6] + 2 KCl

This reaction can be used to remove potassium ferrocyanide from a solution.[citation needed]

A famous reaction involves treatment with ferric salts to give Prussian blue. With the approximate composition KFe2(CN)6, this insoluble but deeply coloured material is the blue of blueprinting.

Applications

Potassium ferrocyanide finds many niche applications in industry. It and the related sodium salt are widely used as anticaking agents for both road salt and table salt. The potassium and sodium ferrocyanides are also used in the purification of tin and the separation of copper from molybdenum ores. Potassium ferrocyanide is used in the production of wine and citric acid.[4]

In the laboratory, potassium ferrocyanide is used to determine the concentration of potassium permanganate, a compound often used in titrations based on redox reactions. Potassium ferrocyanide is used in a mixture with potassium ferricyanide and phosphate buffered solution to provide a buffer for beta-galactosidase, which is used to cleave X-Gal, giving a bright blue visualization where an antibody (or other molecule), conjugated to Beta-gal, has bonded to its target.On reacting with Fe(3) it gives a Prussian blue colour.Thus it is used as a identifying reagent for iron in labs.


Potassium ferrocyanide can be used as a fertilizer for plants.[citation needed]

Prior to 1900 AD, before the invention of the Castner process, potassium ferrocyanide was the most important source of alkali metal cyanides.[4] In this historical process, potassium cyanide was produced by decomposing potassium ferrocyanide:[5]

K4[Fe(CN)6] → 4 KCN + FeC2 + N2

Structure

Like other metal cyanides, solid potassium ferrocyanide, both as the hydrate and anhydrous salts, has a complicated polymeric structure. The polymer consists of octahedral [Fe(CN)6]4- centers crosslinked with K+ ions that are bound to the CN ligands.[7] The K+---NC linkages break when the solid is dissolved in water.

Toxicity

Potassium ferrocyanide is nontoxic, and is not decomposed to cyanide in the body. The toxicity in rats is low, with lethal dose (LD50) at 6400 mg/kg.[2]

See also

References

  1. ^ https://play.google.com/books/reader?printsec=frontcover&output=reader&id=gXwPAAAAYAAJ&pg=GBS.PA8
  2. ^ a b "POTASSIUM FERROCYANIDE MSDS Number: P5763 - Effective Date: 12/08/96". J. T. Baker Inc. Retrieved 2012-04-08.
  3. ^ http://chem.sis.nlm.nih.gov/chemidplus/rn/13943-58-3
  4. ^ a b c Gail, E.; Gos, S.; Kulzer, R.; Lorösch, J.; Rubo, A.; Sauer, M.; Kellens, R.; Reddy, J.; Steier, N.; Hasenpusch, W. (October 2011). "Cyano Compounds, Inorganic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a08_159.pub3.{{cite encyclopedia}}: CS1 maint: multiple names: authors list (link)
  5. ^ a b Von Wagner, Rudolf (1897). Manual of chemical technology. New York: D. Appleton & Co. p. 474 & 477.
  6. ^ Seel, F. (1965). "Sodium Nitrosyl Cyanoferrate". In Brauer, G. (ed.). Handbook of Preparative Inorganic Chemistry. Vol. 2 (2nd ed.). New York: Academic Press. p. 1768. LCCN 63-14307.
  7. ^ Willans, M.J.; Wasylishen, R.E.; McDonald, R. "Polymorphism of potassium ferrocyanide trihydrate as studied by solid-state multinuclear NMR spectroscopy and X-ray diffraction" Inorganic Chemistry 2009, volume 48, p4342-4353