Movatterモバイル変換


[0]ホーム

URL:


Wikipedia

Potassium hydroxide

Potassium hydroxide is aninorganic compound with the formulaKOH, and is commonly calledcaustic potash.

Potassium hydroxide
Crystal structure of KOH
Crystal structure of KOH
Pellets of potassium hydroxide
Pellets of potassium hydroxide
Names
IUPAC name
Potassium hydroxide
Other names
  • Caustic potash
  • Lye
  • Potash lye
  • Potassia
  • Potassium hydrate
  • KOH
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard100.013.802Edit this at Wikidata
EC Number
  • 215-181-3
E numberE525(acidity regulators, ...)
RTECS number
  • TT2100000
UNII
UN number1813
  • InChI=1S/K.H2O/h;1H2/q+1;/p-1 checkY
    Key: KWYUFKZDYYNOTN-UHFFFAOYSA-M checkY
  • InChI=1/K.H2O/h;1H2/q+1;/p-1
    Key: KWYUFKZDYYNOTN-REWHXWOFAT
  • [K+].[OH-]
Properties
KOH
Molar mass56.105 g·mol−1
Appearancewhite solid,deliquescent
Odorodorless
Density2.044 g/cm3 (20 °C)[1]
2.12 g/cm3 (25 °C)[2]
Melting point410[3][4] °C (770 °F; 683 K)
Boiling point1,327 °C (2,421 °F; 1,600 K)
85 g/100 mL (−23.2 °C)
97 g/100 mL (0 °C)
121 g/100 mL (25 °C)
138.3 g/100 mL (50 °C)
162.9 g/100 mL (100 °C)[1][5]
Solubilitysoluble inalcohol,glycerol
insoluble inether, liquidammonia
Solubility inmethanol55 g/100 g (28 °C)[2]
Solubility inisopropanol~14 g / 100 g (28 °C)
Acidity (pKa)14.7[6]
−22.0·10−6 cm3/mol
1.409 (20 °C)
Thermochemistry
65.87 J/mol·K[2]
79.32 J/mol·K[2][7]
−425.8 kJ/mol[2][7]
−380.2 kJ/mol[2]
Hazards
GHS labelling:
GHS05: CorrosiveGHS07: Exclamation mark[8]
Danger
H290,H302,H314[8]
P280,P305+P351+P338,P310[8]
NFPA 704 (fire diamond)
Flash pointnonflammable
Lethal dose or concentration (LD, LC):
273 mg/kg (oral, rat)[10]
NIOSH (US health exposure limits):
PEL (Permissible)
none[9]
REL (Recommended)
C 2 mg/m3[9]
IDLH (Immediate danger)
N.D.[9]
Safety data sheet (SDS)ICSC 0357
Related compounds
Otheranions
Potassium hydrosulfide
Potassium amide
Othercations
Lithium hydroxide
Sodium hydroxide
Rubidium hydroxide
Caesium hydroxide
Related compounds
Potassium oxide
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Along withsodium hydroxide (NaOH), KOH is a prototypicalstrong base. It has many industrial and niche applications, most of which utilize itscaustic nature and its reactivity towardacids. An estimated 700,000 to 800,000tonnes were produced in 2005. KOH is noteworthy as the precursor to most soft and liquidsoaps, as well as numerous potassium-containing chemicals. It is a white solid that is dangerously corrosive.[11]

Properties and structure

edit

KOH exhibits highthermal stability. Because of this high stability and relatively lowmelting point, it is often melt-cast as pellets or rods, forms that have low surface area and convenient handling properties. These pellets become tacky in air because KOH ishygroscopic. Most commercial samples are ca. 90% pure, the remainder being water and carbonates.[11] Itsdissolution in water is stronglyexothermic. Concentrated aqueous solutions are sometimes called potassiumlyes. Even at high temperatures, solid KOH does not dehydrate readily.[12]

Structure

edit

At higher temperatures, solid KOHcrystallizes in theNaClcrystal structure. TheOH group is either rapidly or randomly disordered so that it is effectively a sphericalanion of radius 1.53 Å (betweenCl andF in size). At room temperature, theOH groups are ordered and the environment about theK+ centers is distorted, withK+−OH distances ranging from 2.69 to 3.15 Å, depending on the orientation of the OH group. KOH forms a series of crystallinehydrates, namely the monohydrateKOH ·H2O, the dihydrateKOH · 2H2O and the tetrahydrateKOH · 4H2O.[13]

Reactions

edit

Solubility and desiccating properties

edit

About 112 g of KOHdissolve in 100 mL water at room temperature, which contrasts with 100 g/100 mL for NaOH.[14] Thus on a molar basis, KOH is slightly more soluble than NaOH. Lower molecular-weightalcohols such asmethanol,ethanol, andpropanols are also excellentsolvents. They participate in an acid-base equilibrium. In the case of methanol the potassiummethoxide (methylate) forms:[15]

KOH + CH3OH → CH3OK + H2O

Because of its high affinity for water, KOH serves as adesiccant in the laboratory. It is often used to dry basic solvents, especiallyamines andpyridines.

As a nucleophile in organic chemistry

edit

KOH, like NaOH, serves as a source ofOH, a highlynucleophilic anion that attackspolar bonds in both inorganic and organic materials. Aqueous KOHsaponifiesesters:

KOH + RCOOR' → RCOOK + R'OH

When R is a long chain, the product is called apotassium soap. This reaction is manifested by the "greasy" feel that KOH gives when touched;fats on the skin are rapidly converted to soap andglycerol.

Molten KOH is used to displacehalides and otherleaving groups. The reaction is especially useful foraromatic reagents to give the correspondingphenols.[16]

Reactions with inorganic compounds

edit

Complementary to its reactivity toward acids, KOH attacksoxides. Thus, SiO2 is attacked by KOH to give soluble potassium silicates. KOH reacts withcarbon dioxide to givepotassium bicarbonate:

KOH + CO2 → KHCO3

Manufacture

edit

Historically, KOH was made by addingpotassium carbonate to a strong solution ofcalcium hydroxide (slaked lime). Thesalt metathesis reaction results in precipitation of solidcalcium carbonate, leaving potassium hydroxide in solution:

Ca(OH)2 + K2CO3 → CaCO3 + 2 KOH

Filtering off the precipitated calcium carbonate and boiling down the solution gives potassium hydroxide ("calcinated or caustic potash"). This method of producing potassium hydroxide remained dominant until the late 19th century, when it was largely replaced by the current method of electrolysis ofpotassium chloride solutions.[11] The method is analogous to the manufacture ofsodium hydroxide (seechloralkali process):

2 KCl + 2 H2O → 2 KOH + Cl2 + H2

Hydrogen gas forms as a byproduct on thecathode; concurrently, an anodic oxidation of thechloride ion takes place, formingchlorine gas as a byproduct. Separation of the anodic and cathodic spaces in the electrolysis cell is essential for this process.[17]

Uses

edit

KOH and NaOH can be used interchangeably for a number of applications, although in industry, NaOH is preferred because of its lower cost.

Catalyst for hydrothermal gasification process

edit

In industry, KOH is a good catalyst forhydrothermal gasification process. In this process, it is used to improve the yield of gas and amount of hydrogen in process. For example, production ofcoke (fuel) from coal often produces much coking wastewater. In order to degrade it,supercritical water is used to convert it to the syngas containingcarbon monoxide,carbon dioxide,hydrogen andmethane. Usingpressure swing adsorption, we could separate various gases and then usepower-to-gas technology to convert them to fuel.[18] On the other hand, the hydrothermal gasification process could degrade other waste such as sewage sludge and waste from food factories.

Precursor to other potassium compounds

edit

Many potassium salts are prepared by neutralization reactions involving KOH. The potassium salts ofcarbonate,cyanide,permanganate,phosphate, and various silicates are prepared by treating either the oxides or the acids with KOH.[11] The high solubility ofpotassium phosphate is desirable infertilizers.

Manufacture of soft soaps

edit

Thesaponification offats with KOH is used to prepare the corresponding "potassiumsoaps", which are softer than the more commonsodium hydroxide-derived soaps. Because of their softness and greater solubility, potassium soaps require less water to liquefy, and can thus contain more cleaning agent than liquefied sodium soaps.[19]

As an electrolyte

edit
 
Potassium carbonate, formed from the hydroxide solution leaking from an alkaline battery

Aqueous potassium hydroxide is employed as theelectrolyte inalkaline batteries based onnickel-cadmium,nickel-hydrogen, andmanganese dioxide-zinc. Potassium hydroxide is preferred oversodium hydroxide because its solutions are more conductive.[20] Thenickel–metal hydride batteries in theToyota Prius use a mixture of potassium hydroxide and sodium hydroxide.[21]Nickel–iron batteries also use potassium hydroxide electrolyte.

Food industry

edit

In food products, potassium hydroxide acts as a food thickener, pH control agent and food stabilizer. TheFDA considers it generally safe as a direct food ingredient when used in accordance withGood Manufacturing Practices.[22] It is known in theE number system asE525.

Niche applications

edit

Like sodium hydroxide, potassium hydroxide attracts numerous specialized applications, virtually all of which rely on its properties as a strong chemical base with its consequent ability to degrade many materials. For example, in a process commonly referred to as "chemical cremation" or "resomation", potassium hydroxide hastens the decomposition of soft tissues, both animal and human, to leave behind only the bones and other hard tissues.[23]Entomologists wishing to study the fine structure ofinsectanatomy may use a 10% aqueous solution of KOH to apply this process.[24]

In chemical synthesis, the choice between the use of KOH and the use of NaOH is guided by the solubility or keeping quality of the resultingsalt.

The corrosive properties of potassium hydroxide make it a useful ingredient in agents and preparations that clean anddisinfect surfaces and materials that can themselves resistcorrosion by KOH.[17]

KOH is also used for semiconductor chip fabrication (for exampleanisotropic wet etching).

Potassium hydroxide is often the main active ingredient in chemical "cuticle removers" used inmanicure treatments.

Because aggressive bases like KOH damage thecuticle of thehair shaft, potassium hydroxide is used to chemically assist the removal of hair from animal hides. The hides are soaked for several hours in a solution of KOH and water to prepare them for the unhairing stage of thetanning process. This same effect is also used to weaken human hair in preparation for shaving. Preshave products and some shave creams contain potassium hydroxide to force open the hair cuticle and to act as a hygroscopic agent to attract and force water into the hair shaft, causing further damage to the hair. In this weakened state, the hair is more easily cut by a razor blade.

Potassium hydroxide is used to identify some species offungi. A 3–5% aqueous solution of KOH is applied to the flesh of a mushroom and the researcher notes whether or not the color of the flesh changes. Certain species ofgilled mushrooms,boletes,polypores, andlichens[25] are identifiable based on this color-change reaction.[26]

Safety

edit

Potassium hydroxide is acaustic alkali and its solutions range from irritating to skin and other tissue in low concentrations, to highly corrosive in high concentrations. Eyes are particularly vulnerable, and dust or mist is severely irritating to lungs and can causepulmonary edema.[27] Safety considerations are similar tothose of sodium hydroxide.

The caustic effects arise from being highly alkaline, but if potassium hydroxide isneutralised with a non-toxic acid then it becomes a non-toxic potassium salt. It is approved as a food additive under the code E525.

 
Potassium hydroxide spillage, stained red byphenolphthalein

See also

edit

References

edit
  1. ^abLide, D. R., ed. (2005).CRC Handbook of Chemistry and Physics (86th ed.). Boca Raton, Florida: CRC Press. p. 4-80.ISBN 0-8493-0486-5.
  2. ^abcdef"potassium hydroxide".chemister.ru.Archived from the original on 18 May 2014. Retrieved8 May 2018.
  3. ^Otto, H.W; Seward, R.P. (1964)."Phase equilibria in the potassium hydroxide-sodium hydroxide system".J. Chem. Eng. Data.9 (4):507–508.doi:10.1021/je60023a009.
  4. ^Seward, R.P; Martin, K.E. (1949)."The melting point of potassium hydroxide".J. Am. Chem. Soc.71 (10):3564–3565.doi:10.1021/ja01178a530.
  5. ^Seidell, Atherton; Linke, William F. (1952).Solubilities of Inorganic and Organic Compounds. Van Nostrand. Retrieved2014-05-29.
  6. ^Popov, K.; et al. (2002)."7Li,23Na,39K and133Cs NMR comparative equilibrium study of alkali metal cation hydroxide complexes in aqueous solutions. First numerical value for CsOH formation".Inorganic Chemistry Communications.3 (5):223–225.doi:10.1016/S1387-7003(02)00335-0.ISSN 1387-7003. RetrievedOctober 20, 2018.
  7. ^abZumdahl, Steven S. (2009).Chemical Principles 6th Ed. Houghton Mifflin Company. p. A22.ISBN 978-0-618-94690-7.
  8. ^abcSigma-Aldrich Co.,Potassium hydroxide. Retrieved on 2014-05-18.
  9. ^abcNIOSH Pocket Guide to Chemical Hazards."#0523".National Institute for Occupational Safety and Health (NIOSH).
  10. ^Chambers, Michael."ChemIDplus - 1310-58-3 - KWYUFKZDYYNOTN-UHFFFAOYSA-M - Potassium hydroxide [JAN:NF] - Similar structures search, synonyms, formulas, resource links, and other chemical information".chem.sis.nlm.nih.gov.Archived from the original on 12 August 2014. Retrieved8 May 2018.
  11. ^abcdSchultz, Heinz; Bauer, Günter; Schachl, Erich; Hagedorn, Fritz; Schmittinger, Peter (2005). "Potassium Compounds".Ullmann's Encyclopedia of Industrial Chemistry. Weinheim, Germany: Wiley-VCH.doi:10.1002/14356007.a22_039.ISBN 978-3-527-30673-2.
  12. ^Holleman, A. F; Wiberg, E. (2001).Inorganic Chemistry. San Diego: Academic Press.ISBN 978-0-12-352651-9.
  13. ^Wells, A.F. (1984).Structural Inorganic Chemistry. Oxford: Clarendon Press.ISBN 978-0-19-855370-0.
  14. ^Seidell, Atherton; Linke, William F. (1952).Solubilities of Inorganic and Organic Compounds. Van Nostrand. Retrieved2014-05-29.
  15. ^Platonov, Andrew Y.; Kurzin, Alexander V.; Evdokimov, Andrey N. (2009). "Composition of Vapor and Liquid Phases in the Potassium Hydroxide + Methanol Reaction System at 25 °С".J. Solution Chem.39 (3):335–342.doi:10.1007/s10953-010-9505-1.S2CID 97177429.
  16. ^W. W. Hartman (1923)."p-Cresol".Organic Syntheses.3: 37.doi:10.15227/orgsyn.003.0037;Collected Volumes, vol. 1, p. 175.
  17. ^abRömpp Chemie-Lexikon, 9th Ed. (in German)
  18. ^Chen, Fu; Li, Xiaoxiao; Qu, Junfeng; Ma, Jing; Zhu, Qianlin; Zhang, Shaoliang (2020-01-13)."Gasification of coking wastewater in supercritical water adding alkali catalyst".International Journal of Hydrogen Energy.45 (3):1608–1614.Bibcode:2020IJHE...45.1608C.doi:10.1016/j.ijhydene.2019.11.033.ISSN 0360-3199.S2CID 213336330.
  19. ^K. Schumann; K. Siekmann (2005). "Soaps".Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH.doi:10.1002/14356007.a24_247.ISBN 978-3527306732.
  20. ^D. Berndt; D. Spahrbier (2005). "Batteries".Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH.doi:10.1002/14356007.a03_343.ISBN 978-3527306732.
  21. ^"Toyota Prius Hybrid 2010 Model Emergency Response Guide"(PDF). Toyota Motor Corporation. 2009. Archived fromthe original(PDF) on 2012-03-20.
  22. ^"Compound Summary for CID 14797 - Potassium Hydroxide". PubChem.
  23. ^Green, Margaret (January 1952). "A RAPID METHOD FOR CLEARING AND STAINING SPECIMENS FOR THE DEMONSTRATION OF BONE".The Ohio Journal of Science.52 (1):31–33.hdl:1811/3896.
  24. ^Thomas Eisner (2003).For the Love of Insects. Harvard University Press. p. 71.
  25. ^Elix, J.A.; Stocker-Wörgötter, Elfie (2008). "Chapter 7: Biochemistry and secondary metabolites". In Nash III, Thomas H. (ed.).Lichen Biology (2nd ed.). New York:Cambridge University Press. pp. 118–119.ISBN 978-0-521-69216-8.
  26. ^Testing Chemical ReactionsArchived 2009-10-15 at theWayback Machine at MushroomExpert.com
  27. ^"Hazardous Substance Fact Sheet: Potassium Hydroxide"(PDF).New Jersey Department of Health. Retrieved7 October 2024.

External links

edit
Wikimedia Commons has media related toPotassium hydroxide.

[8]ページ先頭

©2009-2025 Movatter.jp