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Ruthenium(IV) oxide

From Wikipedia, the free encyclopedia
This article is about RuO2. For RuO4, seeRuthenium tetroxide.
Ruthenium(IV) oxide
Names
IUPAC name
Ruthenium(IV) oxide
Other names
Ruthenium dioxide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.031.660Edit this at Wikidata
EC Number
  • 234-840-6
  • Key: WOCIAKWEIIZHES-UHFFFAOYSA-N
  • InChI=1S/2O.Ru
  • O=[Ru]=O
Properties
RuO2
Molar mass133.0688 g/mol
Appearanceblue-black solid
Density6.97 g/cm3
Boiling point1,200 °C (2,190 °F; 1,470 K) sublimates
insoluble
+162.0·10−6 cm3/mol
Structure
Rutile (tetragonal),tP6
P42/mnm, No. 136
Octahedral (RuIV); trigonal planar (O2−)
Hazards
Flash pointNon-flammable
Related compounds
Otheranions
Ruthenium disulfide
Othercations
Osmium(IV) oxide
Ruthenium tetroxide
Supplementary data page
Ruthenium(IV) oxide (data page)
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound

Ruthenium(IV) oxide is theinorganic compound with the formulaRuO2. This black solid is the most common oxide ofruthenium. It is widely used as anelectrocatalyst for producing chlorine, chlorine oxides, and O2.[1] Like many dioxides, RuO2 adopts therutile structure.[2][3]

Preparation

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It is usually prepared by oxidation ofruthenium trichloride. Nearly stoichiometric single crystals of RuO2 can be obtained bychemical vapor transport, using O2 as the transport agent:[4][5]

RuO2 + O2 ⇌ RuO4

Films of RuO2 can be prepared bychemical vapor deposition (CVD) from volatile ruthenium compounds.[6] RuO2 can also be prepared throughelectroplating from a solution of ruthenium trichloride.[7]

Electrostatically stabilized hydrosols of pristine ruthenium dioxide hydrate have been prepared by exploiting the autocatalytic reduction of ruthenium tetroxide in aqueous solution. The resulting particle populations may be controlled to comprise substantially monodisperse, uniform spheres with diameters in the range 40 nm - 160 nm.[8]

Uses

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Ruthenium(IV) oxide is being used as the main component in the catalyst of the Sumitomo-Deacon process which produceschlorine by the oxidation ofhydrogen chloride.[9][10]

RuO2 can be used as catalyst in many other situations. Noteworthy reactions are theFischer–Tropsch process,Haber–Bosch process, and various manifestations offuel cells.

Aspirational and niche applications

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RuO2 is extensively used for the coating of titanium anodes for the electrolytic production of chlorine and for the preparation ofresistors orintegrated circuits.[11][12] Ruthenium oxide resistors can be used as sensitive thermometers in the temperature range .02 < T < 4 K. It can be also used as active material in supercapacitor because it has very high charge transfer capability. Ruthenium oxide has great capacity to store charge when used in aqueous solutions.[13] Average capacities of ruthenium(IV) oxide have reached 650 F/g when insulfuric acid and annealed at temperatures lower than 200 °C.[14] In attempts to optimise its capacitive properties, prior work has looked at the hydration, crystallinity and particle size of ruthenium oxide.

References

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  1. ^Mills, Andrew (1989). "Heterogeneous redox catalysts for oxygen and chlorine evolution".Chemical Society Reviews.18. Royal Society of Chemistry (RSC): 285.doi:10.1039/cs9891800285.ISSN 0306-0012.
  2. ^Wyckoff, R.W.G..Crystal Structures, Vol. 1. Interscience, John Wiley & Sons: 1963.
  3. ^Wells, A. F. (1975),Structural Inorganic Chemistry (4th ed.), Oxford: Clarendon Press
  4. ^Schäfer, Harald; Schneidereit, Gerd; Gerhardt, Wilfried (1963). "Zur Chemie der Platinmetalle. RuO2 Chemischer Transport, Eigenschaften, thermischer Zerfall".Zeitschrift für anorganische und allgemeine Chemie (in German).319 (5–6). Wiley:327–336.Bibcode:1963ZAACh.319..327S.doi:10.1002/zaac.19633190514.ISSN 0044-2313.
  5. ^Rogers, D. B.; Butler, S. R.; Shannon, R. D. (1972). "Single Crystals of Transition-Metal Dioxides".Inorganic Syntheses. Vol. XIII. pp. 135–145.doi:10.1002/9780470132449.ch27.ISBN 9780470132449.
  6. ^Pizzini, S.; Buzzanca, G.; Mari, C.; Rossi, L.; Torchio, S. (1972). "Preparation, structure and electrical properties of thick ruthenium dioxide films".Materials Research Bulletin.7 (5). Elsevier BV:449–462.doi:10.1016/0025-5408(72)90147-x.ISSN 0025-5408.
  7. ^Lee, S. (2003)."Electrochromism of amorphous ruthenium oxide thin films".Solid State Ionics.165 (1–4):217–221.doi:10.1016/j.ssi.2003.08.035.
  8. ^McMurray, H. N. (1993). "Uniform colloids of ruthenium dioxide hydrate evolved by the surface-catalyzed reduction of ruthenium tetroxide".The Journal of Physical Chemistry.97 (30):8039–8045.doi:10.1021/j100132a038.
  9. ^Vogt, Helmut; Balej, Jan; Bennett, John E.; Wintzer, Peter; Sheikh, Saeed Akbar; Gallone, Patrizio (2000-06-15), "Chlorine Oxides and Chlorine Oxygen Acids",Ullmann's Encyclopedia of Industrial Chemistry, Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA,doi:10.1002/14356007.a06_483,ISBN 3527306730
  10. ^Seki, Kohei (2010-05-29). "Development of RuO2/Rutile-TiO2 Catalyst for Industrial HCl Oxidation Process".Catalysis Surveys from Asia.14 (3–4). Springer Science and Business Media LLC:168–175.doi:10.1007/s10563-010-9091-7.ISSN 1571-1013.S2CID 93115959.
  11. ^De Nora, O. (1970). "Anwendung maßbeständiger aktivierter Titan-Anoden bei der Chloralkali-Elektrolyse".Chemie Ingenieur Technik.42 (4). Wiley:222–226.doi:10.1002/cite.330420417.ISSN 0009-286X.
  12. ^Iles, G.S. (1967)."Ruthenium Oxide Glaze Resistors".Platinum Metals Review.11 (4): 126.doi:10.1595/003214067X114126129.
  13. ^Matthey, Johnson (2002)."Nanocrystalline Ruthenium Supercapacitor Material".Platinum Metals Review.46 (3): 105.doi:10.1595/003214002X463105105a. Archived fromthe original on 2015-09-24. Retrieved2013-09-16.
  14. ^Kim, Il-Hwan; Kim, Kwang-Bum;Electrochem. Solid-State Lett.,2001,4, 5, A62-A64

External links

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Ru(0)
Ru(I)
Ru(II)
Ru(II,III)
Ru(III)
Ru(IV)
Ru(V)
Ru(VI)
Ru(VII)
Ru(VIII)
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