Sodium thiosulphate
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| Sodium thiosulfate | |
|---|---|
| |
| |
| IUPAC name | Sodium thiosulfate |
| Other names | Sodium hyposulfite Hyposulphite of soda |
| Identifiers | |
| CAS number | |
| Properties | |
| Molecular formula | Na2S2O3 |
| Molar mass | 158.09774 g/mol |
| Appearance | White crystals |
| Density | 1.667 g/cm³, solid |
| Melting point |
48.3 °C |
| Boiling point |
Decomposes |
| Solubility in water | Very Soluble |
| Basicity (pKb) | N/A |
| Structure | |
| Coordination geometry | Tetrahedral anion |
| Hazards | |
| MSDS | External MSDS |
| EU classification | Non-toxic. |
| NFPA 704 |
|
| R-phrases | R35: Causes severe burns |
| S-phrases | (S1/2) S26 S37/39 S45 |
| Flash point | Non flammable |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) Infobox disclaimer and references | |
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Overview
Sodium thiosulfate (Na2S2O3) (sometimes spelled thiosulphate) is a colorless crystalline compound that is more familiar as the pentahydrate, Na2S2O3•5H2O, an efflorescent, monoclinic crystalline substance also called sodium hyposulfite or “hypo.”
The thiosulfate anion is tetrahedral in shape and is notionally derived by replacing one of the oxygen atoms by a sulfur atom in a sulfate anion. The S-S distance indicates a single bond, implying that the sulfur bears significant negative charge and the S-O interactions have more double bond character. The first protonation of thiosulfate occurs at sulfur.
Industrial production and laboratory synthesis
On an industrial scale, sodium thiosulfate is produced chiefly from liquid waste products of sodium sulfide or sulfur dye manufacture.[1]
Small scale synthesis is by boiling an aqueous solution of sodium sulfite with sulfur.
As such, the anion S2O32− represents a water-soluble form of elemental sulfur.
Principal reactions and applications
Thiosulfate anion characteristically reacts with dilute acids to produce sulfur, sulfur dioxide and water:[1]
- S2O32−(aq) + 2H+(aq) → S(s) + SO2(g) + H2O(l)
This reaction has been employed to generate colloidal sulfur. When the protonation is conducted at low temperatures, H2S2O3 (thiosulfuric acid) can be obtained. It is a strong acid pKa = 0.6, 1.7.
Iodometry
In analytical chemistry, the most important use becomes from the fact thiosulfate anion reacts stoichiometrically with iodine, reducing it to iodide as it is oxidized to tetrathionate:
- 2 S2O32−(aq) + I2(aq) → S4O62−(aq) + 2 I−(aq)
Due to the quantitative nature of this reaction, as well as the fact that Na2S2O3•5H2O has an excellent shelf-life, it is used as a titrant in iodometry. Na2S2O3•5H2O is also a component of iodine clock experiments.
This particular use can be set up to measure the oxygen content of water through a long series of reactions. It is also used in estimating volumetrically, the concentrations of certain compounds in solution (hydrogen peroxide, for instance), and in estimating the chlorine content in commercial bleaching powder and water.
Photographic processing
The terminal sulfur atom in S2O32− binds to soft metals with high affinity. Thus it dissolves silver halides, e.g. AgBr, which is a component of photographic emulsions:
- 2 S2O32− + AgBr → [Ag(S2O3)2]3−) + Br-
In this application to photographic processing, discovered by John Herschel and used for both film and paper processing, sodium thiosulfate is known as a photographic fixer.
Gold extraction
Sodium thiosulfate is one component of an alternative lixiviant to cyanide for extraction of gold.[2] It forms a strong complex with gold(I) ions, [Au(S2O3)2]3-. The advantage of this approach is that thiosulfate is essentially non-toxic and that <link rel="stylesheet" type="text/css" href="http://en.wikipedia.org/w/index.php?title=User:Lupin/navpop.css&action=raw&ctype=text/css&dontcountme=s">ore types that are refractory to gold cyanidation (e.g. carbonaceous or Carlin type ores) can be leached by thiosulfate. Some problems with this alternative process include the high consumption of thiosulfate, and the lack of a suitable recovery technique, since [Au(S2O3)2]3- does not adsorb to activated carbon, which is the standard technique used in gold cyanidation to separate the gold complex from the ore slurry.
Other uses
Sodium thiosulfate is also used:
- As a component in hand warmers and other chemical heating pads that produce heat by exothermic crystallization of a supercooled solution.
- In Bleach
- In pH testing of bleach substances. The universal indicator and any other liquid pH indicator are destroyed by bleach, rendering them useless for testing the pH. If one first adds sodium thiosulfate to such solutions, it will neutralize the color-removing effects of bleach and allow one to test the pH of bleach solutions with liquid indicators. The relevant reaction is akin to the iodine reaction: thiosulfate reduces the hypochlorite (active ingredient in bleach) and in so doing becomes oxidized to sulfate. The complete reaction is:
- 4 NaClO + Na2S2O3 + 2 NaOH → 4 NaCl + 2 Na2SO4 + H2O
- To dechlorinate tap water for aquariums or treat effluent from waste water treatments prior to release into rivers. The reduction reaction is analogous to the iodine reduction reaction. Treatment of tap water requires between 0.1 grams and 0.3 grams of pentahydrated (crystalline) sodium thiosulfate per 10 liters of water.
- To lower chlorine levels in swimming pools and spas following super chlorination.
- To remove iodine stains, e.g. after the explosion of nitrogen triiodide.
- As an antidote to cyanide poisoning. Thiosulfate acts as a sulfur donor for the conversion for cyanide to thiocyanate (which can then be safely excreted in the urine), catalyzed by the enzyme rhodanase.
- In bacteriological water assessment.
- In the tanning of leather.
- To demonstrate the concept of reaction rate in chemistry classes. The thiosulfate ion can decompose into the sulfite ion and a colloidal suspension of sulfur, which is opaque. The equation for this acid-catalysed reaction is as follows:
S2O32−(aq) → SO32−(aq) + S(s) - To demonstrate the concept of supercooling in physics classes. Melted sodium thiosulfate is very easy to overcool to room temperature and when crystallization is forced, the sudden temperature jump to 48.3°C can be experienced by touch.
- As part of patina recipes for copper alloys.
- Often used in pharmaceutical preparations as an anionic surfactant to aid in dispersion.
- Treatment of calciphylaxis in hemodialysis patients with End-Stage Renal Disease
References
- ↑ 1.0 1.1 Holleman, A. F.; Wiberg, E. "Inorganic Chemistry" Academic Press: San Diego, 2001. ISBN 0-12-352651-5
- ↑ Aylmore, M. G.; Muir, D. M. "Thiosulfate Leaching of Gold - a Review", Minerals Engineering, 2001, 14, 135-174
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Some of the initial content on this page may be incorporated in part from copyleft sources in the public domain including wikis such as Wikipedia and AskDrWiki. Drug information for patients came from the The National Library of Medicine. Infectious disease information may have come from the Centers for Disease Control (CDC). Differential Diagnoses are drawn from clinicians as well as an amalgamation of 3 sources: 1.The Disease Database; 2. Kahan, Scott, Smith, Ellen G. In A Page: Signs and Symptoms. Malden, Massachusetts: Blackwell Publishing, 2004:3; 3. Sailer, Christian, Wasner, Susanne. Differential Diagnosis Pocket. Hermosa Beach, CA: Borm Bruckmeir Publishing LLC, 2002:7 .



