|Jmol-3D images||Image 1|
|Molar mass||104.6388 g/mol|
|Appearance||white powder or colourless crystals|
|Melting point||1,115 °C (2,039 °F; 1,388 K)|
|Solubility in water||4.47 g/L (25 °C)
10.7 g/L (100 °C)
|Solubility||insoluble in HF, HCl
soluble in other acid and alkali
|Refractive index (nD)||1.650|
|EU Index||Not listed|
|LD50||3700 mg/kg (rat, oral)|
|Other anions||Germanium disulfide
|Other cations||Carbon dioxide
|Related compounds||Germanium monoxide|
|Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)|
|(what is: / ?)|
Germanium dioxide, also called germanium oxide and germania, is the inorganic compound with the chemical formula GeO2. It is the main commercial source of germanium. forms as a passivation layer on pure germanium in contact with atmospheric oxygen.
The two predominant polymorphs of GeO2 are hexagonal and tetragonal. Hexagonal GeO2 has the same structure as β-quartz, germanium having coordination number 4). Tetragonal GeO2 (the mineral argutite) has the rutile-like structure seen in stishovite. In this motif, germanium has the coordination number 6). An amorphous (glassy) form of GeO2 is similar to fused silica.
Germanium dioxide can be prepared in both crystalline and amorphous forms. At ambient pressure the amorphous structure is formed by a network of GeO4 tetrahedra. At elevated pressure up to approximately 9 GPa the germanium average coordination number steadily increases from 4 to around 5 with a corresponding increase in the Ge-O bond distance. At higher pressures, up to approximately 15 GPa, the germanium coordination number increases to 6 and the dense network structure is composed of GeO6 octahedra. When the pressure is subsequently reduced, the structure reverts to the tetrahedral form. At high pressure, the rutile form converts to an orthorhombic CaCl2 form.
The hexagonal (d = 4.29 g/cm3) form of germanium dioxide is more soluble than the rutile (d = 6.27 g/cm3) form and dissolves to form germanic acid, H4GeO4 or Ge(OH)4. GeO2 is only slightly soluble in acid but dissolves more readily in alkali to give germanates.
The refractive index (1.7) of germanium dioxide and optical dispersion properties makes it useful as an optical material for wide-angle lenses and in optical microscope objective lenses. It is transparent in infrared.
A mixture of silicon dioxide and germanium dioxide ("silica-germania") is used as an optical material for optical fibers and optical waveguides. Controlling the ratio of the elements allows precise control of refractive index. Silica-germania glasses have lower viscosity and higher refractive index than pure silica. Germania replaced titania as the silica dopant for silica fiber, eliminating the need for subsequent heat treatment, which made the fibers brittle.
Germanium dioxide is also used as a catalyst in production of polyethylene terephthalate resin, and for production of other germanium compounds. It is used as a feedstock for production of some phosphors and semiconductor materials.
Furthermore germanium dioxide is used in algaculture as an inhibitor of unwanted diatom growth in algal cultures since a contamination with the comparatively fast-growing diatoms often inhibits the growth of or outcompetes the original algae strains. GeO2 is readily taken up by diatoms and leads to silicon being substituted by germanium in biochemical processes within the diatoms, causing a significant reduction of the diatoms' growth rate or even a complete elimination of the contaminating algae practically without affecting non-diatom algal species. For this application the typically used concentration of germanium dioxide in the culture medium is between 1 and 10 mg/l, depending on the stage of the contamination and the species.
Toxicity and medical
Germanium dioxide has low toxicity, but in higher doses it is nephrotoxic.
- Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 0080379419.
- J W E Drewitt, P S Salmon, A C Barnes, S Klotz, H E Fischer, W A Crichton (2010). "Structure of GeO2 glass at pressures up to 8.6 GPa". Physical Review B 81: 014202. Bibcode:2010PhRvB..81a4202D. doi:10.1103/PhysRevB.81.014202.
- M Guthrie, C A Tulk, C J Benmore, J Xu, J L Yarger, D D Klug, J S Tse, H-k Mao, R J Hemley (2004). "Formation and Structure of a Dense Octahedral Glass". Physical Review Letters 93 (11): 115502. Bibcode:2004PhRvL..93k5502G. doi:10.1103/PhysRevLett.93.115502. PMID 15447351.
- Structural evolution of rutile-type and CaCl2-type germanium dioxide at high pressure, J. Haines, J. M.Léger, C.Chateau, A. S.Pereira, Physics and Chemistry of Minerals, 27, 8 ,(2000), 575–582,doi:10.1007/s002690000092
- Egon Wiberg, Arnold Frederick Holleman, (2001) Inorganic Chemistry, Elsevier ISBN 0-12-352651-5
- Robert D. Brown, Jr. (2000). "Germanium". U.S. Geological Survey.
- Chapter Iii: Optical Fiber For Communications
- Thiele, Ulrich K. (2001). "The Current Status of Catalysis and Catalyst Development for the Industrial Process of Poly(ethylene terephthalate) Polycondensation". International Journal of Polymeric Materials 50 (3): 387–394. doi:10.1080/00914030108035115.
- Robert Arthur Andersen (2005). Algal culturing techniques. Elsevier Academic Press.
- Tao, S.H. and Bolger, P.M. (June 1997). "Hazard Assessment of Germanium Supplements". Regulatory Toxicology and Pharmacology 25 (3): 211–219. doi:10.1006/rtph.1997.1098. PMID 9237323.