Barium sulfide
| Identifiers | |
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3D model (JSmol)
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| ChEBI | |
| ChemSpider | |
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| EC Number |
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| E number | Lua error in Module:Wikidata at line 880: attempt to index field 'wikibase' (a nil value). |
| 13627 | |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| BaS | |
| Molar mass | 169.39 g/mol |
| Appearance | white solid |
| Density | 4.25 g/cm3 [1] |
| Melting point | 2,235[2] °C (4,055 °F; 2,508 K) |
| Boiling point | decomposes |
| 2.88 g/100 mL (0 °C) 7.68 g/100 mL (20 °C) 60.3 g/100 mL (100 °C) (reacts) | |
| Solubility | insoluble in alcohol |
Refractive index (nD)
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2.155 |
| Structure | |
| Halite (cubic), cF8 | |
| Fm3m, No. 225 | |
| Octahedral (Ba2+); octahedral (S2−) | |
| Hazards | |
| GHS labelling: | |
| Warning | |
| H315, H319, H335, H400 | |
| P261, P264, P271, P273, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P391, P403+P233, P405, P501 | |
| NFPA 704 (fire diamond) | |
| Lethal dose or concentration (LD, LC): | |
LD50 (median dose)
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226 mg/kg humans |
| Related compounds | |
Other anions
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Barium oxide Barium selenide Barium telluride Barium polonide |
Other cations
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Beryllium sulfide Magnesium sulfide Calcium sulfide Strontium sulfide Radium sulfide |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Barium sulfide is the inorganic compound with the formula BaS. BaS is the barium compound produced on the largest scale.[3] It is an important precursor to other barium compounds including barium carbonate and the pigment lithopone, ZnS/BaSO4.[4] Like other chalcogenides of the alkaline earth metals, BaS is a short wavelength emitter for electronic displays.[5] It is colorless, although like many sulfides, it is commonly obtained in impure colored forms.
Discovery
[edit | edit source]BaS was prepared by the Italian alchemist Vincenzo Cascariolo (also known as Vincentius or Vincentinus Casciarolus or Casciorolus, 1571–1624) via the thermo-chemical reduction of BaSO4 (available as the mineral barite).[6] It is currently manufactured by an improved version of Cascariolo's process using coke in place of flour and charcoal. This kind of conversion is called a carbothermic reaction:
- BaSO4 + 2C → BaS + 2CO2
and also:
- BaSO4 + 4C → BaS + 4CO
The basic method remains in use today. BaS dissolves in water. These aqueous solutions, when treated with sodium carbonate or carbon dioxide, give a white solid of barium carbonate, a source material for many commercial barium compounds.[7]
According to Harvey (1957),[8] in 1603, Vincenzo Cascariolo used barite, found at the bottom of Mount Paterno near Bologna, in one of his non-fruitful attempts to produce gold. After grinding and heating the mineral with charcoal under reducing conditions, he obtained a persistent luminescent material that soon came to be known as Lapis Boloniensis, or Bolognian stone.[9][10] The phosphorescence of the material obtained by Casciarolo made it a curiosity.[11][12][13]
Preparation
[edit | edit source]A modern procedure proceeds from barium carbonate:[14]
- BaCO3 + H2S → BaS + H2O + CO2
BaS crystallizes with the NaCl structure, featuring octahedral Ba2+ and S2− centres.
The observed melting point of barium sulfide is highly sensitive to impurities.[2]
Safety
[edit | edit source]BaS is quite poisonous, as are related sulfides, such as CaS, which evolve toxic hydrogen sulfide upon contact with water. Barium itself is also toxic.
References
[edit | edit source]- ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
- ^ a b Stinn, C., Nose, K., Okabe, T. et al. Metall and Materi Trans B (2017) 48: 2922. https://doi.org/10.1007/s11663-017-1107-5 Archived 1 January 2024 at the Wayback Machine
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- ^ Holleman, A. F.; Wiberg, E. "Inorganic Chemistry" Academic Press: San Diego, 2001. Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value)..
- ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
- ^ F. Licetus, Litheosphorus, sive de lapide Bononiensi lucem in se conceptam ab ambiente claro mox in tenebris mire conservante, Utini, ex typ. N. Schiratti, 1640. See http://www.chem.leeds.ac.uk/delights/texts/Demonstration_21.htm Archived 13 August 2011 at the Wayback Machine
- ^ Lua error in Module:Citation/CS1/Configuration at line 2172: attempt to index field '?' (a nil value).
- ^ Harvey E. Newton (1957). A History of Luminescence: From the Earliest Times until 1900. Memoirs of the American Physical Society, Philadelphia, J. H. FURST Company, Baltimore, Maryland (USA), Vol. 44, Chapter 1, pp. 11-43.
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