Sodium tetrasulfide

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Sodium tetrasulfide
WikiNa2S4.png
Names
IUPAC name
Sodium tetrasulfide
Other names
disodiumtetrasulphide, sodium sulfide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.031.628 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 234-805-5
PubChem CID
UNII
  • InChI=1S/2Na.H2S4/c;;1-3-4-2/h;;1-2H/q2*+1;/p-2
    Key: ZLCCLBKPLLUIJC-UHFFFAOYSA-L
  • [Na+].[Na+].[S-]SS[S-]
Properties
Na2S4
Molar mass 174.24g/mol
AppearanceDark red, slightly viscous liquid or yellow crystalline powder
Density 1.268 g/cm3 at 15.5 °C
Melting point 275 °C (527 °F; 548 K)
Soluble in water
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
Stable at room temperature, but can be explosive when heated. Reactions with acids or oxidative agents will create gaseous byproducts that would be hazardous if inhaled.
GHS labelling:
GHS-pictogram-flamme.svg GHS-pictogram-acid.svg GHS-pictogram-skull.svg GHS-pictogram-pollu.svg
Danger
H228, H301, H311, H314, H400
P210, P240, P241, P260, P264, P270, P273, P280, P301+P310, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P322, P330, P361, P363, P370+P378, P391, P405, P501
NFPA 704 (fire diamond)
3
1
1
Not applicable
Safety data sheet (SDS) [1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Sodium tetrasulfide is an inorganic compound with the formula Na2S4. It is a yellow-orange solid that dissolves via hydrolysis in water. [2] It is a precursor to some specialty polymers and intermediates in prototypes of the sodium-sulfur battery.

Contents

Synthesis and structure

It is produced through the reaction between elemental sulfur and sodium hydrosulfide in alcoholic solution: [3]

2NaSH + 4 S → Na2S4 + H2S

The polysulfide anions adopt zig-zag chains of sulfur atoms. The S-S distances are about 2.05 Å and the S-S-S-S dihedral angles are around 90°. [4]

Reactions and applications

Upon treatment with acid, it is converted to hydrogen sulfide and elemental sulfur. Treatment with alkylating agents gives organic polysulfides. In one commercial application, it is used to produce the cross-linking agent bis(triethoxysilylpropyl)tetrasulfide: [5]

Na2S4 + 2 ClC3H6Si(OEt)3 → S4[C3H6Si(OEt)3]2 + 2 NaCl

Sometimes as a mixture with other polysulfides, sodium tetrasulfide is used to produce the polymer called thiokol. The reaction involves alkylation with ethylene chloride:

Na2S4 + C2H4Cl2 → 1/n (C2H4)Sx]n + 2 NaCl

These materials, which have the approximate formula (C2H4)Sx]n (x ~ 4), are highly resistant to degradation by solvents and acids. [6]

Related Research Articles

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Sulfur (or sulphur in British English) is a chemical element with the symbol S and atomic number 16. It is abundant, multivalent and nonmetallic. Under normal conditions, sulfur atoms form cyclic octatomic molecules with a chemical formula S8. Elemental sulfur is a bright yellow, crystalline solid at room temperature.

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<span class="mw-page-title-main">Sodium thiosulfate</span> Chemical compound

Sodium thiosulfate (sodium thiosulphate) is an inorganic compound with the formula Na2S2O3.xH2O. Typically it is available as the white or colorless pentahydrate, Na2S2O3·5H2O. The solid is an efflorescent (loses water readily) crystalline substance that dissolves well in water.

<span class="mw-page-title-main">Polysulfide</span>

Polysulfides are a class of chemical compounds containing chains of sulfur atoms. There are two main classes of polysulfides: inorganic and organic. Among the inorganic polysulfides, there are ones which contain anions, which have the general formula S2−
n
. These anions are the conjugate bases of the hydrogen polysulfides H2Sn. Organic polysulfides generally have the formulae R1SnR2, where R = alkyl or aryl.

<span class="mw-page-title-main">Triphenylphosphine</span> Chemical compound

Triphenylphosphine (IUPAC name: triphenylphosphane) is a common organophosphorus compound with the formula P(C6H5)3 and often abbreviated to PPh3 or Ph3P. It is widely used in the synthesis of organic and organometallic compounds. PPh3 exists as relatively air stable, colorless crystals at room temperature. It dissolves in non-polar organic solvents such as benzene and diethyl ether.

<span class="mw-page-title-main">Xanthate</span> Salt that is a metal-thioate/O-esters of dithiocarbonate

Xanthate usually refers to a salt with the formula ROCS
2
M+
(R = alkyl; M+ = Na+, K+), thus they are the metal-thioate/O-esters of dithiocarbonate. The name xanthates is derived from Ancient Greek ξανθός xanthos, meaning “yellowish, golden”, and indeed most xanthate salts are yellow. They were discovered and named in 1823 by Danish chemist William Christopher Zeise. These organosulfur compounds are important in two areas: the production of cellophane and related polymers from cellulose and (in mining) for extraction of certain ores. They are also versatile intermediates in organic synthesis. Xanthate can also refer to the O,S-ester of xanthic acid. These esters have the structure ROC(=S)SR′.

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Calcium sulfide is the chemical compound with the formula CaS. This white material crystallizes in cubes like rock salt. CaS has been studied as a component in a process that would recycle gypsum, a product of flue-gas desulfurization. Like many salts containing sulfide ions, CaS typically has an odour of H2S, which results from small amount of this gas formed by hydrolysis of the salt.

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Sodium sulfide is the chemical compound with the formula Na2S, or more commonly its hydrate Na2S·9H2O. Both the anhydrous and the hydrated salts are colorless solids. They are water-soluble, giving strongly alkaline solutions. When exposed to moist air, Na2S and its hydrates emit hydrogen sulfide, an extremely toxic, flammable and corrosive gas which smells like rotten eggs.

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<span class="mw-page-title-main">Sodium hydrosulfide</span> Chemical compound

Sodium hydrosulfide is the chemical compound with the formula NaSH. This compound is the product of the half-neutralization of hydrogen sulfide with sodium hydroxide (NaOH). NaSH and sodium sulfide are used industrially, often for similar purposes. Solid NaSH is colorless. The solid has an odor of H2S owing to hydrolysis by atmospheric moisture. In contrast with sodium sulfide, which is insoluble in organic solvents, NaSH, being a 1:1 electrolyte, is more soluble.

<span class="mw-page-title-main">Disulfur dichloride</span> Chemical compound

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2
S
. Its existence has been disputed; it may be stable below 0 °C or in suitable environments, but is unstable at room temperature, decomposing into metallic mercury and mercury(II) sulfide.

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4−x
O3−
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and related derivatives where organic groups are attached to one or more O or S. Thiophosphates feature tetrahedral phosphorus(V) centers.

<span class="mw-page-title-main">Sodium polysulfide</span> Chemical compound

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References

  1. "Safety Data Sheet, Sodium Tetrasulfide" (PDF). Pfaltz & Bauer.
  2. Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. p. 365.
  3. D. R. Brush (2000). "Sodium Sulfides". Kirk-Othmer Encyclopedia of Chemical Technology. doi:10.1002/0471238961.1915040902211908.a01. ISBN   0471238961.
  4. R. Tegman "The crystal structure of sodium tetrasulphide, Na2S4" Acta Crystallogr. (1973). B29, 1463-1469 doi : 10.1107/S0567740873004735
  5. Thurn, Friedrich; Meyer-Simon, Eugen; Michel, Rudolf "Verfahren zur Herstellung von Organosiliziumverbindungen (Continuous manufacture of bis[3-(triethoxysilyl)propyl] tetrasulfide)" Ger. Offen. (1973), DE 2212239 A1 19731004.
  6. Sulfides, Polysulfides, and Sulfanes" in Ullmann's Encyclopedia of Industrial Chemistry Ludwig Lange and Wolfgang Triebel, 2000, Wiley-VCH, Weinheim. doi : 10.1002/14356007.a25_443