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Hydrofluoric acid

From Wikipedia, the free encyclopedia
Hydrofluoric acid
Names
IUPAC name
Fluorane[1]
Other names
Fluorhydric acid
Hydronium fluoride
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
EC Number
  • 231-634-8
RTECS number
  • MW7875000
UNII
  • InChI=1S/FH/h1H checkY
    Key: KRHYYFGTRYWZRS-UHFFFAOYSA-N checkY
  • InChI=1/FH/h1H
    Key: KRHYYFGTRYWZRS-UHFFFAOYAC
  • F.O
  • [F-].[OH3+]
Properties
HF (aq)
Appearance Colorless liquid
Density 1.15 g/mL (for 48% soln.)
Acidity (pKa) 3.17[2]
Hazards[3]
GHS labelling:
CorrosiveAcute Toxicity
Danger
H280, H300+H310+H330, H314
P260, P262, P264, P270, P271, P280, P284, P301+P310, P301+P330+P331, P302+P350, P303+P361+P353, P304+P340, P305+P351+P338, P310, P320, P321, P322, P330, P361, P363, P403+P233, P405, P410+P403, P501
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 4: Very short exposure could cause death or major residual injury. E.g. VX gasFlammability 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 hazard ACID: Acid
4
0
0
ACID
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Hydrofluoric acid is a solution of hydrogen fluoride (HF) in water. Solutions of HF are colorless, acidic and highly corrosive. A common concentration is 49% (48-52%) but there are also stronger solutions (e.g. 70%) and pure HF has a boiling point near room temperature. It is used to make most fluorine-containing compounds; examples include the commonly used pharmaceutical antidepressant medication fluoxetine (Prozac) and the material PTFE (Teflon). Elemental fluorine is produced from it. It is commonly used to etch glass and silicon wafers.

Uses

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Production of organofluorine compounds

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The principal use of hydrofluoric acid is in organofluorine chemistry. Many organofluorine compounds are prepared using HF as the fluorine source, including Teflon, fluoropolymers, fluorocarbons, and refrigerants such as freon. Many pharmaceuticals contain fluorine.[4]

Production of inorganic fluorides

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Most high-volume inorganic fluoride compounds are prepared from hydrofluoric acid. Foremost are Na3AlF6, cryolite, and AlF3, aluminium trifluoride. A molten mixture of these solids serves as a high-temperature solvent for the production of metallic aluminium. Other inorganic fluorides prepared from hydrofluoric acid include sodium fluoride and uranium hexafluoride.[4]

Etchant, cleaner

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Wet etching tanks

It is used in the semiconductor industry as a major component of Wright etch and buffered oxide etch, which are used to clean silicon wafers. In a similar manner it is also used to etch glass by treatment with silicon dioxide to form gaseous or water-soluble silicon fluorides. It can also be used to polish and frost glass.[5]

SiO2 + 4 HF → SiF4(g) + 2 H2O
SiO2 + 6 HF → H2SiF6 + 2 H2O

A 5% to 9% hydrofluoric acid gel is also commonly used to etch all ceramic dental restorations to improve bonding.[6] For similar reasons, dilute hydrofluoric acid is a component of household rust stain remover, in car washes in "wheel cleaner" compounds, in ceramic and fabric rust inhibitors, and in water spot removers.[5][7] Because of its ability to dissolve iron oxides as well as silica-based contaminants, hydrofluoric acid is used in pre-commissioning boilers that produce high-pressure steam. Hydrofluoric acid is also useful for dissolving rock samples (usually powdered) prior to analysis. In similar manner, this acid is used in acid macerations to extract organic fossils from silicate rocks. Fossiliferous rock may be immersed directly into the acid, or a cellulose nitrate film may be applied (dissolved in amyl acetate), which adheres to the organic component and allows the rock to be dissolved around it.[8]

Oil refining

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In a standard oil refinery process known as alkylation, isobutane is alkylated with low-molecular-weight alkenes (primarily a mixture of propylene and butylene) in the presence of an acid catalyst derived from hydrofluoric acid. The catalyst protonates the alkenes (propylene, butylene) to produce reactive carbocations, which alkylate isobutane. The reaction is carried out at mild temperatures (0 and 30 °C) in a two-phase reaction.

Production

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Hydrofluoric acid was first prepared in 1771, by Carl Wilhelm Scheele.[9] It is now mainly produced by treatment of the mineral fluorite, CaF2, with concentrated sulfuric acid at approximately 265 °C.

CaF2 + H2SO4 → 2 HF + CaSO4

The acid is also a by-product of the production of phosphoric acid from apatite and fluoroapatite. Digestion of the mineral with sulfuric acid at elevated temperatures releases a mixture of gases, including hydrogen fluoride, which may be recovered.[4]

Because of its high reactivity toward glass, hydrofluoric acid is stored in fluorinated plastic (often PTFE) containers.[4][5]

Properties

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In dilute aqueous solution hydrogen fluoride behaves as a weak acid,[10] Infrared spectroscopy has been used to show that, in solution, dissociation is accompanied by formation of the ion pair H3O+·F−.[11] [12]

H2O + HF ⇌ H3O+⋅F− pKa = 3.17

This ion pair has been characterized in the crystalline state at very low temperature.[13] Further association has been characterized both in solution and in the solid state.[citation needed]

HF + F− ⇌ HF−
2 log K = 0.6

It is assumed that polymerization occurs as the concentration increases. This assumption is supported by the isolation of a salt of a tetrameric anion H
3F−
4[14] and by low-temperature X-ray crystallography.[13] The species that are present in concentrated aqueous solutions of hydrogen fluoride have not all been characterized; in addition to HF−
2 which is known[11] the formation of other polymeric species, H
n−1F−
n, is highly likely.

The Hammett acidity function, H0, for 100% HF was first reported as -10.2,[15] while later compilations show -11, comparable to values near -12 for pure sulfuric acid.[16][17]

Acidity

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Unlike other hydrohalic acids, such as hydrochloric acid, hydrogen fluoride is only a weak acid in dilute aqueous solution.[18] This is in part a result of the strength of the hydrogen–fluorine bond, but also of other factors such as the tendency of HF, H
2O, and F−
 anions to form clusters.[19] At high concentrations, HF molecules undergo homoassociation to form polyatomic ions (such as bifluoride, HF−
2) and protons, thus greatly increasing the acidity.[20] This leads to protonation of very strong acids like hydrochloric, sulfuric, or nitric acids when using concentrated hydrofluoric acid solutions.[21] Although hydrofluoric acid is regarded as a weak acid, it is very corrosive, even attacking glass when hydrated.[20]

Dilute solutions are weakly acidic with an acid ionization constant Ka = 6.6×10−4 (or pKa = 3.18),[10] in contrast to corresponding solutions of the other hydrogen halides, which are strong acids (pKa < 0). However concentrated solutions of hydrogen fluoride are much more strongly acidic than implied by this value, as shown by measurements of the Hammett acidity function H0(or "effective pH"). During self ionization of 100% liquid HF the H0 was first measured as −10.2[15] and later compiled as −11, comparable to values near −12 for sulfuric acid.[16][17]

In thermodynamic terms, HF solutions are highly non-ideal, with the activity of HF increasing much more rapidly than its concentration. The weak acidity in dilute solution is sometimes attributed to the high H—F bond strength, which combines with the high dissolution enthalpy of HF to outweigh the more negative enthalpy of hydration of the fluoride ion.[22] Paul Giguère and Sylvia Turrell[11][12] have shown by infrared spectroscopy that the predominant solute species in dilute solution is the hydrogen-bonded ion pair H3O+·F−.[23]

H2O + HF ⇌ H3O+⋅F−

With increasing concentration of HF the concentration of the hydrogen difluoride ion also increases.[11] The reaction

3 HF ⇌ HF−
2 + H2F+

is an example of homoconjugation.

Health and safety

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A hydrofluoric acid burn of the hand
Main article: Hydrofluoric acid burn

In addition to being a highly corrosive liquid, hydrofluoric acid is also a powerful contact poison. Since it can penetrate tissue, poisoning can occur readily through exposure of skin or eyes, inhalation, or ingestion. Symptoms of exposure to hydrofluoric acid may not be immediately evident, and this can provide false reassurance to victims, causing them to delay medical treatment.[24] Despite its irritating vapor, HF may reach dangerous levels without an obvious odor.[5] It interferes with nerve function, meaning that burns may not initially be painful. Accidental exposures can go unnoticed, delaying treatment and increasing the extent and seriousness of the injury.[24] Symptoms of HF exposure include irritation of the eyes, skin, nose, and throat, eye and skin burns, rhinitis, bronchitis, pulmonary edema (fluid buildup in the lungs), and bone damage[25] due to HF strongly interacting with calcium in bones.[26] In a concentrated form, HF can cause severe tissue destruction through lesions and mucous membrane damage, but dilute HF is still dangerous because of its high lipid affinity, leading to cellular death of nerves, blood vessels, tendons, bones, and other tissues.[27]

Hydrofluoric burns are treated with a calcium gluconate gel.

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See also

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References

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  1. ^ Favre, Henri A.; Powell, Warren H., eds. (2014). Nomenclature of Organic Chemistry: IUPAC Recommendations and Preferred Names 2013. Cambridge: The Royal Society of Chemistry. p. 131. ISBN 9781849733069.
  2. ^ Harris, Daniel C. (2010). Quantitative Chemical Analysis (8th international ed.). New York: W. H. Freeman. pp. AP14. ISBN 978-1429263092.
  3. ^ "Hydrofluoric Acid". PubChem. National Institute of Health. Retrieved October 12, 2017.
  4. ^ a b c d Aigueperse, Jean; Mollard, Paul; Devilliers, Didier; Chemla, Marius; Faron, Robert; Romano, René; Cuer, Jean Pierre (2000). "Fluorine Compounds, Inorganic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a11_307. ISBN 3527306730.
  5. ^ a b c d "Hydrogen Fluoride/Hydrofluoric Acid: Systemic Agent". Emergency Response Safety and Health Database. NIOSH - CDC. May 12, 2011. Archived from the original on Dec 7, 2015. Retrieved 2015-12-04.
  6. ^ Craig, Robert (2006). Craig's restorative dental materials. St. Louis, Mo: Mosby Elsevier. ISBN 0-323-03606-6. OCLC 68207297.
  7. ^ Strachan, John (January 1999). "A deadly rinse: The dangers of hydrofluoric acid". Professional Carwashing & Detailing. 23 (1). Archived from the original on April 25, 2012.
  8. ^ Edwards, D. (1982). "Fragmentary non-vascular plant microfossils from the late Silurian of Wales". Botanical Journal of the Linnean Society. 84 (3): 223–256. doi:10.1111/j.1095-8339.1982.tb00536.x.
  9. ^ Greenwood, Norman N.; Earnshaw, Alan (1984). Chemistry of the Elements. Oxford: Pergamon Press. p. 921. ISBN 978-0-08-022057-4.
  10. ^ a b Ralph H. Petrucci; William S. Harwood; Jeffry D. Madura (2007). General chemistry: principles and modern applications. Pearson/Prentice Hall. p. 691. ISBN 978-0-13-149330-8. Retrieved 22 August 2011.
  11. ^ a b c d Giguère, Paul A.; Turrell, Sylvia (1980). "The nature of hydrofluoric acid. A spectroscopic study of the proton-transfer complex H3O+...F−". J. Am. Chem. Soc. 102 (17): 5473. doi:10.1021/ja00537a008.
  12. ^ a b Radu Iftimie; Vibin Thomas; Sylvain Plessis; Patrick Marchand; Patrick Ayotte (2008). "Spectral Signatures and Molecular Origin of Acid Dissociation Intermediates". J. Am. Chem. Soc. 130 (18): 5901–7. doi:10.1021/ja077846o. PMID 18386892.
  13. ^ a b Mootz, D. (1981). "Crystallochemical Correlate to the Anomaly of Hydrofluoric Acid". Angew. Chem. Int. Ed. Engl. 20 (123): 791. doi:10.1002/anie.198107911.
  14. ^ Bunič, Tina; Tramšek, Melita; Goreshnik, Evgeny; Žemva, Boris (2006). "Barium trihydrogen tetrafluoride of the composition Ba(H3F4)2: The first example of homoleptic HF metal environment". Solid State Sciences. 8 (8): 927–931. Bibcode:2006SSSci...8..927B. doi:10.1016/j.solidstatesciences.2006.02.045.
  15. ^ a b Hyman, Herbert H.; Kilpatrick, Martin; Katz, Joseph J. (1957). "The Hammett Acidity Function H0 for Hydrofluoric Acid Solutions". Journal of the American Chemical Society. 79 (14). American Chemical Society (ACS): 3668–3671. doi:10.1021/ja01571a016. ISSN 0002-7863.
  16. ^ a b Jolly, William L. (1984). Modern Inorganic Chemistry. McGraw-Hill. p. 203. ISBN 0-07-032768-8. OCLC 22861992.
  17. ^ a b Cotton, F. A.; Wilkinson, G. (1988). Advanced Inorganic Chemistry (5th ed.). New York: Wiley. p. 109. ISBN 0-471-84997-9. OCLC 16580057.
  18. ^ Wiberg, Egon; Wiberg, Nils; Holleman, Arnold Frederick (2001). Inorganic Chemistry. San Diego: Academic Press. p. 425. ISBN 978-0-12-352651-9.
  19. ^ Clark, Jim (2002). "The acidity of the hydrogen halides". Retrieved 4 September 2011.
  20. ^ a b Chambers, C.; Holliday, A. K. (1975). Modern inorganic chemistry (An intermediate text) (PDF). The Butterworth Group. pp. 328–329. Archived from the original (PDF) on 2013-03-23.
  21. ^ Hannan, Henry J. (2010). Course in chemistry for IIT-JEE 2011. Tata McGraw Hill Education Private Limited. pp. 15–22. ISBN 9780070703360.
  22. ^ C. E. Housecroft and A. G. Sharpe "Inorganic Chemistry" (Pearson Prentice Hall, 2nd ed. 2005), p. 170.
  23. ^ Cotton & Wilkinson (1988), p. 104
  24. ^ a b Yamashita M, Yamashita M, Suzuki M, Hirai H, Kajigaya H (2001). "Ionophoretic delivery of calcium for experimental hydrofluoric acid burns". Crit. Care Med. 29 (8): 1575–8. doi:10.1097/00003246-200108000-00013. PMID 11505130. S2CID 45595073.
  25. ^ "NIOSH Pocket Guide to Chemical Hazards – Hydrogen fluoride". CDC. Retrieved 2015-11-28.
  26. ^ "Hydrofluoric Acid Fact Sheet" (PDF). Department of Environmental Safety, Sustainability & Risk. University of Maryland. Retrieved 11 March 2024. the HF molecule can cause deep tissue damage, including destruction of the bone. ... when fluoride ions bind to calcium and magnesium
  27. ^ Bajraktarova-Valjakova E, Korunoska-Stevkovska V, Georgieva S, Ivanovski K, Bajraktarova-Misevska C, Mijoska A, Grozdanov A (2018). "Hydrofluoric Acid: Burns and Systemic Toxicity, Protective Measures, Immediate and Hospital Medical Treatment". Open Access Macedonian Journal of Medical Sciences. 6 (11): 2257–69. doi:10.3889/oamjms.2018.429 (inactive 1 November 2024). PMC 6290397. PMID 30559898.{{cite journal}}: CS1 maint: DOI inactive as of November 2024 (link)
  28. ^ "How much of the science in Breaking Bad is real?". BBC News. 16 August 2013. Archived from the original on 17 August 2023.
  29. ^ Hare, Jonathan (1 May 2011). "Breaking Bad II – acid bath disposal of bodies". education in chemistry. Royal Society of Chemistry. Archived from the original on 10 June 2023.
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