Sulfur trioxide (alternative spelling sulphur trioxide, also known as nisso sulfan) is the chemical compound with the formula SO3. It has been described as "unquestionably the most important economically" sulfur oxide. It is prepared on an industrial scale as a precursor to sulfuric acid.
|Preferred IUPAC name
|Systematic IUPAC name
Sulfuric anhydride, Sulfur(VI) oxide
3D model (JSmol)
|UN number||UN 1829|
CompTox Dashboard (EPA)
|Molar mass||80.066 g/mol|
|Appearance||Colorless to white crystalline solid which will fume in air. Colorless liquid and gas.|
|Odor||Varies. Vapor is pungent; like sulfur dioxide. Mist is odorless.|
|Density||1.92 g/cm3, liquid|
|Melting point||16.9 °C (62.4 °F; 290.0 K)|
|Boiling point||45 °C (113 °F; 318 K)|
|Reacts to give sulfuric acid|
Std enthalpy of
|Main hazards||Highly corrosive|
|Safety data sheet||ICSC 1202|
|GHS Signal word||Danger|
|P261, P280, P305+P351+P338, P310|
|NFPA 704 (fire diamond)|
|Lethal dose or concentration (LD, LC):|
LC50 (median concentration)
|rat, 4 hr 375 mg/m3|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Sulfur trioxide exists in several forms - gaseous monomer, crystalline trimer, and solid polymer. Sulfur trioxide is a solid at just below room temperature with a relatively narrow liquid range. Gaseous SO3 is the primary precursor to acid rain.
Molecular structure and bondingEdit
The molecule SO3 is trigonal planar. As predicted by VSEPR theory, its structure belongs to the D3h point group. The sulfur atom has an oxidation state of +6 and a formal charge of 0. The S-O bonding is delocalized with all three S-O bond lengths equal at 1.42 Å. The electrical dipole moment of gaseous sulfur trioxide is zero.
Sulfur trioxide undergoes many reactions.
- Hydration and hydrofluorination
SO3 is the anhydride of H2SO4. Thus, it is susceptible to hydration:
- SO3 + H2O → H2SO4 (ΔHf = −200 kJ mol−1) Gaseous sulfur trioxide fumes profusely even in a relatively dry atmosphere owing to formation of a sulfuric acid mist.
- SO3 + HF → FSO3H
SO3 reacts with dinitrogen pentoxide to give the nitronium salt of pyrosulfate:
- 2 SO3 + N2O5 → [NO2]2S2O7
- SO3 + SCl2 → SOCl2 + SO2
- Lewis acid
- Sulfonating agent
Sulfur trioxide is a potent sulfonating agent, i.e. it adds SO3 groups to substrates. Often the substrates are organic. For activated substrates, Lewis base adducts of sulfur trioxide are effective sulfonating agents.
The direct oxidation of sulfur dioxide to sulfur trioxide in air proceeds very slowly:
- SO2 + 1⁄2O2 = SO3 ΔH=-198.4
Industrially SO3 is made by the contact process. Sulfur dioxide is produced by the burning of sulfur or iron pyrite (a sulfide ore of iron). After being purified by electrostatic precipitation, the SO2 is then oxidised by atmospheric oxygen at between 400 and 600 °C over a catalyst. A typical catalyst consists of vanadium pentoxide (V2O5) activated with potassium oxide K2O on kieselguhr or silica support. Platinum also works very well but is too expensive and is poisoned (rendered ineffective) much more easily by impurities. The majority of sulfur trioxide made in this way is converted into sulfuric acid.
- Dehydration at 315 °C:
- 2 NaHSO4 → Na2S2O7 + H2O
- Cracking at 460 °C:
- Na2S2O7 → Na2SO4 + SO3
In contrast, KHSO4 does not undergo the same reaction.
Sulfur trioxide is a reagent in sulfonation reactions. These processes afford detergents, dyes, and pharmaceuticals. Sulfur trioxide is generated in situ from sulfuric acid or is used as a solution in the acid.
B2O3 stabilized Sulfur trioxide was traded by Baker & Adamson under the tradename "Sulfan" in the 20th century.
Structure of SO3Edit
Both liquid and gaseous SO3 exists in an equilibrium between the monomer and the cyclic trimer. The nature of solid SO3 is complex and at least 3 polymorphs are known, with conversion between them being dependent on traces of water.
If SO3 is condensed above 27 °C, then α-SO3 forms, which has a melting point of 62.3 °C. α-SO3 is fibrous in appearance. Structurally, it is the polymer [S(=O)2(μ-O)]n. Each end of the polymer is terminated with OH groups. β-SO3, like the alpha form, is fibrous but of different molecular weight, consisting of an hydroxyl-capped polymer, but melts at 32.5 °C. Both the gamma and the beta forms are metastable, eventually converting to the stable alpha form if left standing for sufficient time. This conversion is caused by traces of water.
Relative vapor pressures of solid SO3 are alpha < beta < gamma at identical temperatures, indicative of their relative molecular weights. Liquid sulfur trioxide has a vapor pressure consistent with the gamma form. Thus heating a crystal of α-SO3 to its melting point results in a sudden increase in vapor pressure, which can be forceful enough to shatter a glass vessel in which it is heated. This effect is known as the "alpha explosion".
Along with being an oxidizing agent, sulfur trioxide is highly corrosive. It reacts violently with water to produce highly corrosive sulfuric acid.
- Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. pp. 703–704. ISBN 978-0-08-037941-8.
- "SULFUR TRIOXIDE CAMEO Chemicals NOAA". Cameochemicals.noaa.gov.
- Lerner, L. (2011). Small-Scale Synthesis of Laboratory Reagents with Reaction Modeling. CRC Press. p. 10. ISBN 9781439813133. LCCN 2010038460.
- "Substance:Sulfur trioxide - Learn Chemistry Wiki". Rsc.org.
- "Sulfur trioxide 227692" (PDF). SO3. Archived from the original on 2020-09-01. Retrieved 1 September 2020.
- Thomas Loerting; Klaus R. Liedl (2000). "Toward elimination of descrepancies between theory and experiment: The rate constant of the atmospheric conversion of SO3 to H2SO4". Proceedings of the National Academy of Sciences of the United States of America. 97 (16): 8874–8878. Bibcode:2000PNAS...97.8874L. doi:10.1073/pnas.97.16.8874. PMC 16788. PMID 10922048.
- "The Manufacture of Sulfuric Acid and Superphosphate" (PDF). Chemical Processes in New Zealand.
- Cotton, F. Albert; Wilkinson, Geoffrey; Murillo, Carlos A.; Bochmann, Manfred (1999), Advanced Inorganic Chemistry (6th ed.), New York: Wiley-Interscience, ISBN 0-471-19957-5
- Weil, J. K.; Bistline Jr., R. G.; Stirton, A. J. (1956). "α-Sulfopalmitic Acid". Organic Syntheses. 36: 83. doi:10.15227/orgsyn.036.0083.
- Rondestvedt Jr., Christian S.; Bordwell, F. G. (1954). "Sodium β-Styrenesulfonate and β-Styrenesulfonyl Chloride". Organic Syntheses. 34: 85. doi:10.15227/orgsyn.034.0085.
- Hermann Müller "Sulfuric Acid and Sulfur Trioxide" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim. 2000 doi:10.1002/14356007.a25_635
- K.J. de Vries; P.J. Gellings (May 1969). "The thermal decomposition of potassium and sodium-pyrosulfate". Journal of Inorganic and Nuclear Chemistry. 31 (5): 1307–1313. doi:10.1016/0022-1902(69)80241-1.
- "How to make sulfur trioxide - YouTube". www.youtube.com. Retrieved 1 September 2020.
- Habashi, Fathi; Dugdale, Raymond (June 1973) [1972-11-06]. "The Action of Sulfur Trioxide on Chalcopyrite". Metallurgical and Materials Transactions. B-4 (6): 1553–1556. Bibcode:1973MT......4.1553H. doi:10.1007/BF02668007 (inactive 31 October 2021). p. 1553:
Sulfur trioxide used was pure, colorless liquid SO3 marketed under the trade name Sulfan by Baker and AdamsonCS1 maint: DOI inactive as of October 2021 (link)
- Lovejoy, R. W.; Colwell, J. H.; Eggers, D. F.; Halsey, G. D. (February 1962). "Infrared Spectrum and Thermodynamic Properties of Gaseous Sulfur Trioxide". The Journal of Chemical Physics. 36 (3): 612–617. Bibcode:1962JChPh..36..612L. doi:10.1063/1.1732581.
- Holleman, Arnold Frederik; Wiberg, Egon (2001), Wiberg, Nils (ed.), Inorganic Chemistry, translated by Eagleson, Mary; Brewer, William, San Diego/Berlin: Academic Press/De Gruyter, ISBN 0-12-352651-5
- Westrik, R.; Mac Gillavry, C. H. (1941). "The crystal structure of the ice-like form of sulphur trioxide (γ-modification)". Recueil des Travaux Chimiques des Pays-Bas. 60 (11): 794–810. doi:10.1002/recl.19410601102.
- Merck Index of Chemicals and Drugs, 9th ed. monograph 8775