Sodium dithionite explained

Sodium dithionite (also known as sodium hydrosulfite) is a white crystalline powder with a sulfurous odor. Although it is stable in dry air, it decomposes in hot water and in acid solutions.

Structure

The structure has been examined by Raman spectroscopy and single-crystal X-ray diffraction. The dithionite dianion has C symmetry, with almost eclipsed with a 16° O-S-S-O torsional angle. In the dihydrated form, the dithionite anion has gauche 56° O-S-S-O torsional angle.[1]

A weak S-S bond is indicated by the S-S distance of 239 pm, which is elongated by ca. 30 pm relative to a typical S-S bond. Because this bond is fragile, the dithionite anion dissociates in solution into the [SO<sub>2</sub>] radicals, as has been confirmed by EPR spectroscopy. It is also observed that 35S undergoes rapid exchange between S2O42− and SO2 in neutral or acidic solution, consistent with the weak S-S bond in the anion.

Preparation

Sodium dithionite is produced industrially by reduction of sulfur dioxide. Approximately 300,000 tons were produced in 1990.[2] The route using zinc powder is a two-step process:

2SO2 + Zn → ZnS2O4

ZnS2O4 + 2NaOH → Na2S2O4 + Zn(OH)2

The sodium borohydride method obeys the following stoichiometry:

NaBH4 + 8NaOH + 8SO2 → 4Na2S2O4 + NaBO2 + 6H2OEach equivalent of H reduces two equivalents of sulfur dioxide. Formate has also been used as the reductant.

Properties and reactions

Hydrolysis

Sodium dithionite is stable when dry, but aqueous solutions deteriorate due to the following reaction:

2 S2O42− + H2O → S2O32− + 2 HSO3This behavior is consistent with the instability of dithionous acid. Thus, solutions of sodium dithionite cannot be stored for a long period of time.[3]

Anhydrous sodium dithionite decomposes to sodium sulfate and sulfur dioxide above 90 °C in the air. In absence of air, it decomposes quickly above 150 °C to sodium sulfite, sodium thiosulfate, sulfur dioxide and trace amount of sulfur.

Redox reactions

Sodium dithionite is a reducing agent. At pH 7, the potential is -0.66 V compared to the normal hydrogen electrode. Redox occurs with formation of bisulfite:[4]

S2O42- + 2 H2O → 2 HSO3 + 2 e + 2 H+

Sodium dithionite reacts with oxygen:

Na2S2O4 + O2 + H2O → NaHSO4 + NaHSO3These reactions exhibit complex pH-dependent equilibria involving bisulfite, thiosulfate, and sulfur dioxide.

With organic carbonyls

In the presence of aldehydes, sodium dithionite reacts either to form α-hydroxy-sulfinates at room temperature or to reduce the aldehyde to the corresponding alcohol above a temperature of 85 °C.[5] [6] Some ketones are also reduced under similar conditions.

Applications

Industry

Being water-soluble, sodium dithionite is used as a reducing agent in some industrial dyeing processes. In the case of sulfur dyes and vat dyes, an otherwise water-insoluble dye can be reduced into a water-soluble alkali metal salt (e.g. indigo dye).[7]

Sodium dithionite can also be used for water treatment, aquarium water conditioners, gas purification, cleaning, and stripping. It has also been applied as a sulfonating agent. In addition to the textile industry, this compound is used in industries concerned with leather, foods, polymers, photography, and many others, often as a decolourising agent. It is even used domestically as a decoloring agent for white laundry, when it has been accidentally stained by way of a dyed item slipping into the high temperature washing cycle. It is usually available in 5 gram sachets termed hydrosulfite after the antiquated name of the salt.

It is the active ingredient in "Iron Out Rust Stain Remover", a commercial rust product.[8]

Laboratory

Sodium dithionite is often used in physiology experiments as a means of lowering solutions' redox potential (Eo' -0.66 V vs SHE at pH 7).[9] Potassium ferricyanide is usually used as an oxidizing chemical in such experiments (Eo' ~ .436 V at pH 7). In addition, sodium dithionite is often used in soil chemistry experiments to determine the amount of iron that is not incorporated in primary silicate minerals. Hence, iron extracted by sodium dithionite is also referred to as "free iron." The strong affinity of the dithionite ion for bi- and trivalent metal cations (M2+, M3+) allows it to enhance the solubility of iron, and therefore dithionite is a useful chelating agent.

Aqueous solutions of sodium dithionite were once used to produce 'Fieser's solution' for the removal of oxygen from a gas stream.[10] Pyrithione can be prepared in a two-step synthesis from 2-bromopyridine by oxidation to the N-oxide with a suitable peracid followed by substitution using sodium dithionite to introduce the thiol functional group.[11]

Photography

It is used in Kodak fogging developer, FD-70. This is used in the second step in processing black and white positive images, for making slides. It is part of the Kodak Direct Positive Film Developing Outfit.[12]

Safety

The wide use of sodium dithionite is attributable in part to its low toxicity at 2.5 g/kg (rats, oral).[2]

See also

External links

Notes and References

  1. J. B.. D. R.. J. T.. P. E.. K. L.. Weinrach. D. S.. D. W.. A structural study of sodium dithionite and its ephemeral dihydrate: A new conformation for the dithionite ion. Journal of Crystallographic and Spectroscopic Research. 22. 3. 291–301. 1992. 10.1007/BF01199531. Meyer. Guy. Michalski. Carter. Grubisha. Bennett. 97124638.
  2. Book: José Jiménez Barberá . Adolf Metzger . Manfred Wolf . Sulfites, Thiosulfates, and Dithionites . Ullmann's Encyclopedia of Industrial Chemistry . 15 June 2000 . Wiley Online Library . 10.1002/14356007.a25_477. 978-3527306732 .
  3. Book: Inorganic Chemistry, 3rd Edition. Chapter 16: The group 16 elements. Catherine E. Housecroft. Alan G. Sharpe. Pearson. 2008. 978-0-13-175553-6. 520.
  4. Mayhew, S. G.. The Redox Potential of Dithionite and SO−2 from Equilibrium Reactions with Flavodoxins, Methyl Viologen and Hydrogen plus Hydrogenase. European Journal of Biochemistry. 2008. 85. 2. 535–547. 10.1111/j.1432-1033.1978.tb12269.x. 648533. free.
  5. J. Org. Chem., 1980, 45 (21), pp 4126–4129, http://pubs.acs.org/doi/abs/10.1021/jo01309a011
  6. Web site: Aldehyde sulfoxylate systemic fungicides. google.com. 27 April 2018. live. https://web.archive.org/web/20180427175353/https://patents.google.com/patent/US5270058A/en. 27 April 2018.
  7. Božič. Mojca. Kokol. Vanja. Ecological alternatives to the reduction and oxidation processes in dyeing with vat and sulphur dyes. Dyes and Pigments. 2008. 76. 2. 299–309. 10.1016/j.dyepig.2006.05.041.
  8. Web site: The Best Rust Removers for Restoring Every Surface . 23 March 2023 .
  9. MAYHEW. Stephen G.. The Redox Potential of Dithionite and SO-2 from Equilibrium Reactions with Flavodoxins, Methyl Viologen and Hydrogen plus Hydrogenase. European Journal of Biochemistry. 85. 2. 1978. 535–547. 0014-2956. 10.1111/j.1432-1033.1978.tb12269.x. 648533. free.
  10. Kenneth L. Williamson "Reduction of Indigo: Sodium Hydrosulfite as a Reducing Agent" J. Chem. Educ., 1989, volume 66, p 359.
  11. Encyclopedia: 1-Hydroxypyridine-2(1H)-thione. David W.. Knight. Jens. Hartung. 15 September 2006. 10.1002/047084289X.rh067.pub2. John Wiley & Sons. Encyclopedia of Reagents for Organic Synthesis. 1-Hydroxypyridine-2(1H)-thione. 978-0471936237.
  12. Web site: Kodak Direct Positive Film 5246 . 125px.com . Kodak . 6 November 2019.
  13. Web site: Sodium dithionite - ipcs inchem . www.inchem.org . 15 June 2018 . Berliln, Germany . 2004 . 17 April 2018 . https://web.archive.org/web/20180417180337/http://www.inchem.org/documents/sids/sids/7775146.pdf . dead .