Potassium sulfate

Potassium sulfate
Arcanite
Arcanite
Potassium sulfate
Names
Other names
Potassium sulphate
Identifiers
CAS Number
  • 7778-80-5 checkY
3D model (JSmol)
  • Interactive image
ChEBI
  • CHEBI:32036 checkY
ChEMBL
  • ChEMBL2021424 checkY
ChemSpider
  • 22915 checkY
ECHA InfoCard 100.029.013 Edit this at Wikidata
EC Number
  • 231-915-5
E number E515(i) (acidity regulators, ...)
KEGG
  • D01726 checkY
PubChem CID
  • 24507
RTECS number
  • TT5900000
UNII
  • 1K573LC5TV checkY
CompTox Dashboard (EPA)
  • DTXSID6029701 Edit this at Wikidata
InChI
  • InChI=1S/2K.H2O4S/c;;1-5(2,3)4/h;;(H2,1,2,3,4)/q2*+1;/p-2 checkY
    Key: OTYBMLCTZGSZBG-UHFFFAOYSA-L checkY
  • InChI=1/2K.H2O4S/c;;1-5(2,3)4/h;;(H2,1,2,3,4)/q2*+1;/p-2
    Key: OTYBMLCTZGSZBG-NUQVWONBAU
  • [K+].[K+].[O-]S([O-])(=O)=O
Properties
Chemical formula
K2SO4
Molar mass 174.259 g/mol
Appearance White solid
Odor odorless
Density 2.66 g/cm3[1]
Melting point 1,069[2] °C (1,956 °F; 1,342 K)
Boiling point 1,689 °C (3,072 °F; 1,962 K)
111 g/L (20 °C)
120 g/L (25 °C)
240 g/L (100 °C)
1.32 (120 g/L)
Solubility slightly soluble in glycerol
insoluble in acetone, alcohol, CS2
−67.0·10−6 cm3/mol
1.495
Structure
orthorhombic
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Irritant
GHS labelling:
GHS07: Exclamation mark
Warning
H318
P280, P305+P351+P338, P310
Flash point Non-flammable
Lethal dose or concentration (LD, LC):
6600 mg/kg (oral, rat)[3]
Safety data sheet (SDS) External MSDS
Related compounds
Other anions
Potassium selenate
Potassium tellurate
Other cations
Lithium sulfate
Sodium sulfate
Rubidium sulfate
Caesium sulfate
Related compounds
Potassium hydrogen sulfate
Potassium sulfite
Potassium bisulfite
Potassium persulfate
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 ?)
Infobox references
Chemical compound

Potassium sulfate (US) or potassium sulphate (UK), also called sulphate of potash (SOP), arcanite, or archaically potash of sulfur, is the inorganic compound with formula K2SO4, a white water-soluble solid. It is commonly used in fertilizers, providing both potassium and sulfur.

History

Potassium sulfate (K2SO4) has been known since early in the 14th century. It was studied by Glauber, Boyle, and Tachenius. In the 17th century, it was named arcanuni or sal duplicatum, as it was a combination of an acid salt with an alkaline salt. It was also known as vitriolic tartar and Glaser's salt or sal polychrestum Glaseri after the pharmaceutical chemist Christopher Glaser who prepared it and used medicinally.[4][5]

Known as arcanum duplicatum ("double secret") or panacea duplicata in pre-modern medicine, it was prepared from the residue (caput mortuum) left over from the production of aqua fortis (nitric acid, HNO3) from nitre (potassium nitrate, KNO3) and oil of vitriol (sulphuric acid, H2SO4) via Glauber's process:

2 KNO3 + H2SO4 → 2 HNO3 + K2SO4

The residue was dissolved in hot water, filtered, and evaporated to a cuticle. It was then left to crystallise. It was used as a diuretic and sudorific.[6]

According to Chambers's Cyclopedia, the recipe was purchased for five hundred thalers by Charles Frederick, Duke of Holstein-Gottorp. Schroder, the duke's physician, wrote wonders of its great uses in hypochondriacal cases, continued and intermitting fevers, stone, scurvy, and more.[6]

Natural resources

The mineral form of potassium sulfate, arcanite, is relatively rare. Natural resources of potassium sulfate are minerals abundant in the Stassfurt salt. These are cocrystallizations of potassium sulfate and sulfates of magnesium, calcium, and sodium.

Relevant minerals are:

The potassium sulfate can be separated from some of these minerals, like kainite, because the corresponding salt is less soluble in water.

Kieserite, MgSO4·H2O, can be combined with a solution of potassium chloride to produce potassium sulfate.

Production

Approximately 1.5 million tons were produced in 1985, typically by the reaction of potassium chloride with sulfuric acid, analogous to the Mannheim process for producing sodium sulfate.[7] The process involves intermediate formation of potassium bisulfate, an exothermic reaction that occurs at room temperature:

KCl + H2SO4 → HCl + KHSO4

The second step of the process is endothermic, requiring energy input:

KCl + KHSO4 → HCl + K2SO4

Structure and properties

Two crystalline forms are known. Orthorhombic β-K2SO4 is the common form, but it converts to α-K2SO4 above 583 °C.[7] These structures are complex, although the sulfate adopts the typical tetrahedral geometry.[8]

  • Structure of β-K2SO4.
    Structure of β-K2SO4.
  • Coordination sphere of one of two types of K+ site.
    Coordination sphere of one of two types of K+ site.
  • SO4 environment in β-K2SO4.
    SO4 environment in β-K2SO4.

It does not form a hydrate, unlike sodium sulfate. The salt crystallizes as double six-sided pyramids, classified as rhombic. They are transparent, very hard and have a bitter, salty taste. The salt is soluble in water, but insoluble in solutions of potassium hydroxide (sp. gr. 1.35), or in absolute ethanol.

Uses

The dominant use of potassium sulfate is as a fertilizer. K2SO4 does not contain chloride, which can be harmful to some crops. Potassium sulfate is preferred for these crops, which include tobacco and some fruits and vegetables. Crops that are less sensitive may still require potassium sulfate for optimal growth if the soil accumulates chloride from irrigation water.[9]

The crude salt is also used occasionally in the manufacture of glass. Potassium sulfate is also used as a flash reducer in artillery propellant charges. It reduces muzzle flash, flareback and blast overpressure.

It is sometimes used as an alternative blast media similar to soda in soda blasting as it is harder and similarly water-soluble.[10]

Potassium sulfate can also be used in pyrotechnics in combination with potassium nitrate to generate a purple flame.

A 5% solution of potassium sulfate was used in the beginning of the 20th century as a topical mosquito repellent.[citation needed]

Reactions

Acidification

Potassium hydrogen sulfate (also known as potassium bisulfate), KHSO4, is readily produced by reacting K2SO4 with sulfuric acid. It forms rhombic pyramids, which melt at 197 °C (387 °F). It dissolves in three parts of water at 0 °C (32 °F). The solution behaves much as if its two congeners, K2SO4 and H2SO4, were present side by side of each other uncombined; an excess of ethanol the precipitates normal sulfate (with little bisulfate) with excess acid remaining.

The behavior of the fused dry salt is similar when heated to several hundred degrees; it acts on silicates, titanates, etc., the same way as sulfuric acid that is heated beyond its natural boiling point does. Hence it is frequently used in analytical chemistry as a disintegrating agent. For information about other salts that contain sulfate, see sulfate.

References

  1. ^ Patnaik, Pradyot (2002). Handbook of Inorganic Chemicals. McGraw-Hill. ISBN 978-0-07-049439-8.
  2. ^ Windholtz, M; Budavari, S, eds. (1983). The Merck Index. Rahway, New Jersey: Merck & Co.
  3. ^ Chambers, Michael. "Potassium sulfate RN: 7778-80-5". ChemIDplus. United States National Library of Medicine.
  4. ^ De Milt, Clara (1942). "Christopher Glaser". Journal of Chemical Education. 19 (2): 53. Bibcode:1942JChEd..19...53D. doi:10.1021/ed019p53.
  5. ^ van Klooster, H. S. (1959). "Three centuries of Rochelle salt". Journal of Chemical Education. 36 (7): 314. Bibcode:1959JChEd..36..314K. doi:10.1021/ed036p314.
  6. ^ a b Public Domain Chambers, Ephraim, ed. (1728). "Arcanum duplicatum". Cyclopædia, or an Universal Dictionary of Arts and Sciences. Vol. 1 (1st ed.). James and John Knapton, et al. p. *125.
  7. ^ a b Schultz, H.; Bauer, G.; Schachl, E.; Hagedorn, F.; Schmittinger, P. (2005). "Potassium Compounds". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a22_039. ISBN 3527306730.
  8. ^ Gaultier, M.; Pannetier, G. (1968). "Structure cristalline de la forme 'basse température' du sulfate de potassium K2SO4-beta" [Crystal structure of the "low temperature" β-form of potassium sulfate]. Bulletin de la Société Chimique de France (in French). 1: 105–112.
  9. ^ United Nations Industrial Development Organization; International Fertilizer Development Center (1998). Fertilizer manual (3rd ed.). Dordrecht, Netherlands: Kluwer Academic. ISBN 978-0-7923-5032-3.
  10. ^ "Super K (Potassium Sulphate)". American Surface Prep. Archived from the original on 9 December 2014. Retrieved 7 December 2014.

External links

  • mindat.org: Arcanite
  • webmineral: Arcanite
  • v
  • t
  • e
H, (pseudo)halogens
chalcogens
  • K2O
  • KOH
  • K2O2
  • KO2
  • KO3
  • K2S
  • KHS
  • K2SO3
  • KHSO3
  • K2SO4
  • KHSO4
  • KHSO5
  • K2S2O3
  • K2S2O5
  • K2S2O7
  • K2S2O8
  • K2Se
  • K2SeO3
  • K2SeO4
  • K2Te
  • K2TeO3
  • K2TeO4
  • K2Po
pnictogens
  • K3N
  • KNH2
  • KN3
  • KNO2
  • KNO3
  • K3P
  • KH2PO3
  • K3PO4
  • K2HPO4
  • KH2PO4
  • KPF6
  • KAsO2
  • K3AsO4
  • K2HAsO4
  • KH2AsO4
B, C group
  • B4K2O7
  • K2CO3
  • KHCO3
  • K2SiO3
  • K2SiF6
  • K2Al2O4
  • K2Al2B2O7
trans metals
  • K2PtCl4
  • K2Pt(CN)4
  • K2TiF6
  • K2PtCl6
  • K2ReCl6
  • K2ZrF6
  • K4Fe(CN)6
  • K3Fe(CN)6
  • K3Fe(C2O4)3
  • K2FeO4
  • K2MnO4
  • KMnO4
  • K3CrO4
  • K2CrO4
  • K3CrO8
  • KCrO3Cl
  • K2Cr2O7
  • K2Cr3O10
  • K2Cr4O13
  • K4Mo2Cl8
organic
  • KHCO2
  • KCH3CO2
  • KCF3CO2
  • K2C2O4
  • KHC2O4
  • KC12H23O2
  • KC18H35O2
  • C3H2K2O4
  • C4H6KO4
  • C5H7KO4
  • v
  • t
  • e
Compounds containing the sulfate group (SO2−4)
H2SO4 He
Li2SO4 BeSO4 B2S2O9
-BO3
+BO3
esters
ROSO3
(RO)2SO2
+CO3
+C2O4
(NH4)2SO4
[N2H5]HSO4
(NH3OH)2SO4
NOHSO4
+NO3
HOSO4 +F Ne
Na2SO4
NaHSO4
MgSO4 Al2(SO4)3
Al2SO4(OAc)4
Si +PO4 SO2−4
HSO3HSO4
(HSO4)2
+SO3
+Cl Ar
K2SO4
KHSO4
CaSO4 Sc2(SO4)3 TiOSO4 VSO4
V2(SO4)3
VOSO4
CrSO4
Cr2(SO4)3
MnSO4 FeSO4
Fe2(SO4)3
CoSO4
Co2(SO4)3
NiSO4
Ni2(SO4)3
CuSO4
Cu2SO4
[Cu(NH3)4(H2O)]SO4
ZnSO4 Ga2(SO4)3 Ge As +SeO3 Br Kr
RbHSO4
Rb2SO4
SrSO4 Y2(SO4)3 Zr(SO4)2 Nb2O2(SO4)3 MoO(SO4)2
MoO2(SO4)
Tc Ru(SO4)2 Rh2(SO4)3 PdSO4 Ag2SO4
AgSO4
CdSO4 In2(SO4)3 SnSO4
Sn(SO4)2
Sb2(SO4)3 Te +IO3 Xe
Cs2SO4
CsHSO4
BaSO4 * Lu2(SO4)3 Hf Ta WO(SO4)2 Re2O5(SO4)2 OsSO4
Os2(SO4)3
Os(SO4)2
IrSO4
Ir2(SO4)3
Pt2(SO4)54– AuSO4
Au2(SO4)3
Hg2SO4
HgSO4
Tl2SO4
Tl2(SO4)3
PbSO4
Pb(SO4)2
Bi2(SO4)3 PoSO4
Po(SO4)2
At Rn
Fr RaSO4 ** Lr Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
 
* La2(SO4)3 Ce2(SO4)3
Ce(SO4)2
Pr2(SO4)3 Nd2(SO4)3 Pm2(SO4)3 Sm2(SO4)3 EuSO4
Eu2(SO4)3
Gd2(SO4)3 Tb2(SO4)3 Dy2(SO4)3 Ho2(SO4)3 Er2(SO4)3 Tm2(SO4)3 Yb2(SO4)3
** Ac2(SO4)3 Th(SO4)2 Pa U2(SO4)3
U(SO4)2
UO2SO4
Np(SO4)2 Pu(SO4)2 Am2(SO4)3 Cm2(SO4)3 Bk Cf2(SO4)3 Es Fm Md No
  • v
  • t
  • e
Sulfides and
disulfides
  • Al2S3
  • As2S2
  • As2S3
  • As2S5
  • As4S4
  • Au2S
  • Au2S3
  • B2S3
  • BaS
  • BeS
  • Bi2S3
  • CS2
  • C3S2
  • C6S6
  • CaS
  • CdS
  • CeS
  • CoS
  • Cr2S3
  • CSSe
  • CSTe
  • CuFeS2
  • CuS
  • D2S
  • Dy2S3
  • Er2S3
  • EuS
  • FeS2
  • GaS
  • H2S
  • HfS2
  • HgS
  • In2S3
  • K2S
  • LaS
  • LiS
  • MgS
  • MoS2
  • MoS3
  • NaHS
  • Na2S
  • NH4HS
  • NiS
  • P4Sx
  • PbS
  • PbS2
  • PSCl3
  • PSI3
  • PtS
  • ReS2
  • Re2S7
  • SiS
  • SrS
  • TlS
  • VS
  • SeS2
  • S2U
  • WS2
  • WS3
  • Sb2S3
  • Sb2S5
  • Sb4S3O3
  • Sm2S3
  • Y2S3
  • ZrS2
  • La
    2
    O
    2
    S
  • Gd
    2
    O
    2
    S
Sulfur halides
  • S2Br2
  • SBr2
  • S2Cl2
  • SCl2
  • SCl4
  • SF2
  • SF4
  • S2F10
  • SF6
  • S2I2
Sulfur oxides
and oxyhalides
  • SO2
  • SO3
  • SOBr2
  • SOCl2
  • SOF2
  • SOF4
  • H2S3O6
  • H2SO3
  • H2SO4
  • H2S2O7
  • H2SO5
Sulfites
  • CdSO3
  • K2SO3
Sulfates
  • Ag2SO4
  • CaSO4
  • CuSO4
  • Cs2SO4
  • Er2(SO4)3
  • Eu2(SO4)3
  • HgSO4
  • K2SO4
  • KAl(SO4)2
  • NaAl(SO4)2
  • RaSO4
  • SnSO4
  • SrSO4
  • Ti(SO4)2
  • Tm2(SO4)3
  • Yb2(SO4)3
  • Zr(SO4)2
Thiocyanates
Organic compounds
  • C2H4S
  • C2H6S3
  • C4H4S
  • C32H66S2
  • CHCl3S
  • C2H3SN
Authority control databases: National Edit this at Wikidata
  • Germany