Ammonium sulfate

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Ammonium sulfate
Ammonium sulfate.png
Ball-and-stick model of two ammonium cations and one sulfate anion
Names
IUPAC name
Ammonium tetraoxosulfate (VI)
Other names
Ammonium sulfate
Ammonium sulfate (2:1)
Diammonium sulfate
Sulfuric acid diammonium salt
Mascagnite
Actamaster
Dolamin
Identifiers
7783-20-2 YesY
ChemSpider 22944 YesY
Jmol 3D model Interactive image
KEGG D08853 YesY
UNII SU46BAM238 YesY
  • InChI=1S/2H3N.H2O4S/c;;1-5(2,3)4/h2*1H3;(H2,1,2,3,4) YesY
    Key: BFNBIHQBYMNNAN-UHFFFAOYSA-N YesY
  • InChI=1/2H3N.H2O4S/c;;1-5(2,3)4/h2*1H3;(H2,1,2,3,4)
    Key: BFNBIHQBYMNNAN-UHFFFAOYAI
  • O=S(=O)(O)O.N.N
Properties
(NH4)2SO4
Molar mass 132.14 g/mol
Appearance Fine white hygroscopic granules or crystals.
Density 1.769 g/cm3 (20 °C)
Melting point 235 to 280 °C (455 to 536 °F; 508 to 553 K) (decomposes)
70.6 g/100 mL (0 °C)

74.4 g/100 mL (20 °C)
103.8 g/100 mL (100 °C)[1]
Solubility insoluble in acetone, alcohol and ether
79.2% (30 °C)
Vapor pressure {{{value}}}
Related compounds
Other anions
Ammonium thiosulfate
Ammonium sulfite
Ammonium bisulfate
Ammonium persulfate
Other cations
Sodium sulfate
Potassium sulfate
Related compounds
Ammonium iron(II) sulfate
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
YesY verify (what is YesYN ?)
Infobox references

Ammonium sulfate (American English; ammonium tetraoxosulfate (VI) is the IUPAC-recommended spelling;[citation needed] and ammonium sulphate in British English), (NH4)2SO4, is an inorganic salt with a number of commercial uses. The most common use is as a soil fertilizer. It contains 21% nitrogen and 24% sulfur.

Uses

The primary use of ammonium sulfate is as a fertilizer for alkaline soils. In the soil the ammonium ion is released and forms a small amount of acid, lowering the pH balance of the soil, while contributing essential nitrogen for plant growth. The main disadvantage to the use of ammonium sulfate is its low nitrogen content relative to ammonium nitrate, which elevates transportation costs.[2]

It is also used as an agricultural spray adjuvant for water-soluble insecticides, herbicides, and fungicides. There, it functions to bind iron and calcium cations that are present in both well water and plant cells. It is particularly effective as an adjuvant for 2,4-D (amine), glyphosate, and glufosinate herbicides.

Laboratory use

In biochemistry, ammonium sulfate precipitation is a common method for purifying proteins by selective precipitation; Ammonium sulfate is extremely soluble in water and so can make very concentrated solutions, which can "salt out" proteins, causing their precipitation at particular concentrations. This provides a convenient and simple means to fractionate complex protein mixtures.[3] As such, ammonium sulfate is also listed as an ingredient for many United States vaccines per the Center for Disease Control.[4]

In the analysis of rubber lattices, volatile fatty acids are analyzed by precipitating rubber with a 35% ammonium sulfate solution, which leaves a clear liquid from which volatile fatty acids are regenerated with sulfuric acid and then distilled with steam. Selective precipitation with ammonium sulfate, opposite to the usual precipitation technique which uses acetic acid, does not interfere with the determination of volatile fatty acids.[5]

Food additive

As a food additive, ammonium sulfate is considered generally recognized as safe (GRAS) by the U.S. Food and Drug Administration,[6] and in the European Union it is designated by the E number E517. It is used as an acidity regulator in flours and breads.[7][8][9]

Other uses

Ammonium sulfate is used on a small scale in the preparation of other ammonium salts, especially ammonium persulfate.

A saturated solution of ammonium sulfate in heavy water (2H2O) is used as an external standard in sulfur (33S) NMR spectroscopy with shift value of 0 ppm.

Ammonium sulfate has also been used in flame retardant compositions acting much like diammonium phosphate. As a flame retardant, it increases the combustion temperature of the material, decreases maximum weight loss rates, and causes an increase in the production of residue or char.[10] Its flame retardant efficacy can be enhanced by blending it with ammonium sulfamate.[citation needed]

Ammonium sulfate has been used as a wood preservative, but due to its hygroscopic nature, this use has been largely discontinued because of associated problems with metal fastener corrosion, dimensional instability, and finish failures.

Preparation

Ammonium sulfate is made by treating ammonia, often as a by-product from coke ovens, with sulfuric acid:

2 NH3 + H2SO4 → (NH4)2SO4

A mixture of ammonia gas and water vapor is introduced into a reactor that contains a saturated solution of ammonium sulfate and about 2 to 4% of free sulfuric acid at 60 °C. Concentrated sulfuric acid is added to keep the solution acidic, and to retain its level of free acid. The heat of reaction keeps reactor temperature at 60 °C. Dry, powdered ammonium sulfate may be formed by spraying sulfuric acid into a reaction chamber filled with ammonia gas. The heat of reaction evaporates all water present in the system, forming a powdery salt. Approximately 6000M tons were produced in 1981.[2]

Ammonium sulfate also is manufactured from gypsum (CaSO4·2H2O). Finely divided gypsum is added to an ammonium carbonate solution. Calcium carbonate precipitates as a solid, leaving ammonium sulfate in the solution.

(NH4)2CO3 + CaSO4 → (NH4)2SO4 + CaCO3

Ammonium sulfate occurs naturally as the rare mineral mascagnite in volcanic fumaroles and due to coal fires on some dumps.[11]

Properties

Ammonium sulfate becomes ferroelectric at temperatures below -49.5 °C. At room temperature it crystallises in the orthorhombic system, with cell sizes of a = 7.729 Å, b = 10.560 Å, c = 5.951 Å. When chilled into the ferrorelectric state, the symmetry of the crystal changes to space group Pna21.[12]

Reactions

Ammonium sulfate decomposes upon heating above 250 °C, first forming ammonium bisulfate. Heating at higher temperatures results in decomposition into ammonia, nitrogen, sulfur dioxide, and water.[13]

As a salt of a strong acid (H2SO4) and weak base (NH3), its solution is acidic; pH of 0.1 M solution is 5.5. In aqueous solution the reactions are those of NH4+ and SO4−2 ions. For example, addition of barium chloride, precipitates out barium sulfate. The filtrate on evaporation yields ammonium chloride.

Ammonium sulfate forms many double salts (ammonium metal sulfates) when its solution is mixed with equimolar solutions of metal sulfates and the solution is slowly evaporated. With trivalent metal ions, alums such as ferric ammonium sulfate are formed. Double metal sulfates include ammonium cobaltous sulfate, ferrous diammonium sulfate, ammonium nickel sulfate which are known as Tutton's salts and ammonium ceric sulfate.[2] Anhydrous double sulfates of ammonium also occur in the Langbeinites family.

Legislation and Control

In November 2009, a ban on ammonium sulfate, ammonium nitrate and calcium ammonium nitrate fertilizers was imposed in the former Malakand Division—comprising the Upper Dir, Lower Dir, Swat, Chitral and Malakand districts of the North West Frontier Province (NWFP) of Pakistan, by the NWFP government, following reports that they were used by militants to make explosives. In January 2010, these substances were also banned in Afghanistan for the same reason.[14]

See also

Ammonium sulfate precipitation

References

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  2. 2.0 2.1 2.2 Karl-Heinz Zapp "Ammonium Compounds" in Ullmann's Encyclopedia of Industrial Chemistry 2012, Wiley-VCH, Weinheim. doi:10.1002/14356007.a02_243
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  5. ASTM Standard Specification for Rubber Concentrates D 1076-06
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Further reading

External links