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Sodium stannate

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Sodium stannate
White powder of sodium stannate
White powder of sodium stannate
Molecular Structure of Sodium Stannate
Names
IUPAC name
disodium dioxido(oxo)tin
Other names
  • Sodium stannate(IV)
  • Sodium tin oxide
  • Disodium stannate
  • Disodium tin trioxide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.031.554 Edit this at Wikidata
EC Number
  • 235-030-5
RTECS number
  • JN6345000
  • InChI=1S/2Na.3O.Sn/q2*+1;;2*-1; checkY
    Key: TVQLLNFANZSCGY-UHFFFAOYSA-N checkY
  • InChI=1S/2Na.3O.Sn/q2*+1;;2*-1;
    Key: UHOVQNZJYSORNB-UHFFFAOYAH
  • [Na+].[Na+].[O-][Sn]([O-])=O
Properties
Na2SnO3 (Anhydrous)

Na2SnO3·3H2O (Trihydrate) Na2Sn(OH)6 (Hexahydroxide)

Molar mass 212.687739 g/mol (Anhydrous)

266.73 g/mol (Trihydrate)

Appearance Colorless hexagonal plate crystal. White Crystalline powder.
Density 4.68 g/cm3
Melting point 140°C (Trihydrate)
277 g/L
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Very hazardous irritant in the cases of eye contact, ingestion, inhalation. Hazardous irritant and permeator by skin contact.
NFPA 704 (fire diamond)
NFPA 704 four-colored diamondHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogen
2
0
0
Flash point 57°C
Lethal dose or concentration (LD, LC):
2132 mg/kg [Mouse]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Sodium Stannate is a hexagonal plate crystalline solid composed of a stannate anion bonded ionically to two sodium cations.

Sodium stannate is primarily used in industries that deal with the electro-deposition of tin onto metal surfaces such as copper. The production processes of tin, tin alloys, mordant, ceramics and glass make use of sodium stannate to some degree as well. It plays an important role as a catalyst in the process of dehydrogenation.

Properties

Sodium stannate is a white to off white powder. It's structure is that of a hexagonal plate crystalline solid. Several other forms of sodium stannate exist such as trihydrated sodium stannate and sodium stannate hexahydroxide. Sodium stannate is relatively stable.

History

A large scale production of alkali metal stannates was innovated by Richard Horn in the late 1970s. Richard Horn's patented process of making alkali metal stannates provided a more efficient and less expensive way to prepare alkali metal stannates at a higher commercial rate.

In today's industries, inorganic stannic, or tin(IV), compounds are used primarily in electrolytic solutions for electroplating tin and tin alloys. Sodium stannate is used fundamentally for the removal of arsenic and lead in the metallurgic industry.[2]

Production

Alkali metal stannate compounds are prepared in an electrochemical process by dissolving a tin anode in the alkali metal hydroxide solution present in an electrodialytic cell. This process forms an alkali metal stannite compound. A permselective ion exchange membrane is used to prevent the sodium stannate migrating to the cathode chamber of the electrolytic cell. The oxidation of the alkali metal stannite with oxygen O2 gas produces an alkali metal stannate.

Hazards

Sodium Stannate is a fairly harmless chemical, but it does have the potential to be dangerous if used incorrectly. It is very hazardous if it comes in contact with eyes, is ingested, or inhaled in large amounts. It is toxic to lungs and mucous membranes. Prolonged or repeated exposure to sodium stannate will cause organ and epithelial damage. If contact with eyes occurs, remove contact lenses and flush immediately. If ingested, drink water and do not induce vomiting. Wash with soap while scrubbing after use. It is not a fire hazard nor is it a carcinogen.

Uses

Sodium stannate is actually a common ingredient that is found in many household products. Many at home hair bleaching kits and dental whitening products prefer to use sodium stannate for its safe bleaching properties. Some facial cleansers and oral pain medicines also contain sodium stannate.

Sodium stannate is also a very effective chemical satbilizer of hydrogen peroxide.[3] This property makes it an ideal chemical to aid in the disinfecting of contact lenses. Hydrogen peroxide can act in harmful ways by being corrosive if it is in an unfavorable concentration. To stabilize the hydrogen peroxide and make it safe to use on contacts, sodium stannate is added to the solution to ensure the safety of your eyes. It aids in both preventing microbe growth and chemicals burning your eyes.

http://chemindustry.ru/Hydrogen_Peroxide_pharma.php

Reactions

Sodium Stannate has been proven in lab to promote aluminum/water reactions that produce hydrogen. When paired with sodium hydroxide, NaOH, sodium stannate can greatly affect hydrogen generation from the aluminum/water system. Also, small amounts of sodium stannate will cause a tremendous decrease in NaOH concentration for optimal performance conditions for the aluminum/water system.[4] This comes at the expense of the experimental apparatus. The sodium stannate can be an excellent catalyst.

Also, sodium stannate can generate superbasic sites on its surface by simple thermal treatment with pure N2.[5] After going through calcinations, or an aerobic heat treatment process performed on metals and other solid materials to induce a thermal decomposition, at 623 K, there are great superbasic sites on sodium stannate. These can be up to 0.254 mmol/g. This property of superbacisity was also further established by employing the “1-hexene as well as cyclohexa-1,4-diene double bond isomerization reactions.”[6] This is because of the better LUMO that is the surface O2-. It has been determined that catalytic efficiency of sodium stannate is related to the property of superbasicity of the sodium stannate.[7]

References

  1. ^ "Sodium stannate trihydrate MSDS". Science Lab. Retrieved 13 November 2012.
  2. ^ "Sodium Stannate". Todini and Co s.p.a. Retrieved 20 October 2012.
  3. ^ "Sodium Stannate Guide". GoodGuide. GoogGuide, Inc. Retrieved 14 November 2012.
  4. ^ Dai, Hong-Bin (1 January 2011). "Reaction of aluminium with alkaline sodium stannate solution as a controlled source of hydrogen". Energy & Environmental Science. 4 (6): 2206. doi:10.1039/C1EE00014D. Retrieved 13 November 2012. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  5. ^ Zhang, Shu-Guo (1 October 2011). "Superbasic sodium stannate as catalyst for dehydrogenation, Michael addition and transesterification reactions". Applied Catalysis A: General. 406 (1–2): 113–118. doi:10.1016/j.apcata.2011.08.015. Retrieved 13 November 2012. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  6. ^ Ibid
  7. ^ Ibid