Gibbsite, Al(OH)3, is one of the mineral forms of aluminium hydroxide. It is often designated as γ-Al(OH)3[2]: 2 (but sometimes as α-Al(OH)3[3]). It is also sometimes called hydrargillite (or hydrargyllite).
| Gibbsite | |
|---|---|
 Gibbsite | |
| General | |
| Category | Hydroxide minerals |
| Formula (repeating unit) | Al(OH)3 |
| IMA symbol | Gbb[1] |
| Strunz classification | 4.FE.10 |
| Crystal system | Monoclinic |
| Crystal class | Prismatic (2/m) (same H-M symbol) |
| Space group | P21/n |
| Identification | |
| Mohs scale hardness | 2.5–3 |
| Specific gravity | 2.35 |
Gibbsite is an important ore of aluminium in that it is one of three main phases that make up the rock bauxite.
Gibbsite has three named structural polymorphs or polytypes: bayerite (designated often as α-Al(OH)3,[2]: 2 but sometimes as β-Al(OH)3)[citation needed], doyleite, and nordstrandite. Gibbsite can be monoclinic or triclinic, while bayerite is monoclinic.[2]: 13 Doyleite and nordstrandite are triclinic forms.[2]: 13
Structure
editThe structure of gibbsite is interesting and analogous to the basic structure of the micas. The basic structure forms stacked sheets of linked octahedra. Each octahedron is composed of an aluminium ion bonded to six hydroxide groups, and each hydroxide group is shared by two aluminium octahedra.[4] One third of the potential octahedral spaces are missing a central aluminium. The result is a neutral sheet: with aluminium as a +3 ion and hydroxide a −1 ion, the net cationic charge of one aluminium per six hydroxides is (+3)/6 = +1/2, and likewise the net anionic charge of one hydroxide per two aluminium atoms is (−1)/2 = −1/2. The lack of a charge on the gibbsite sheets means that there is no charge to retain ions between the sheets and act as a "glue" to keep the sheets together. The sheets are only held together by weak residual bonds and this results in a very soft easily cleaved mineral.[citation needed]
Gibbsite's structure is closely related to the structure of brucite, Mg(OH)2. However the lower charge in brucite's magnesium (+2) as opposed to gibbsite's aluminium (+3) does not require that one third of the octahedrons be vacant of a central ion in order to maintain a neutral sheet. The different symmetry of gibbsite and brucite is due to the different way that the layers are stacked.
It is the gibbsite layer that in a way forms the "floor plan" for the mineral corundum, Al2O3. The basic structure of corundum is identical to gibbsite except the hydroxides are replaced by oxygen. Since oxygen has a charge of −2 the layers are not neutral and require that they must be bonded to other aluminiums above and below the initial layer producing the framework structure that is the structure of corundum.
Gibbsite is interesting for another reason because it is often found as a part of the structure of other minerals. The neutral aluminium hydroxide sheets are found sandwiched between silicate sheets in important clay groups: the illite, kaolinite, and montmorillonite/smectite groups. The individual aluminium hydroxide layers are identical to the individual layers of gibbsite and are referred to as the gibbsite layers.[5]
The lattice parameters for gibbsite depending upon the particular method used to measure or calculate them and are therefore displayed as ranges below. An Al-Al interlayer spacing of 0.484 or 0.494 nm has been reported.[6]
| Crystal system | Molecules per unit cell | Lattice parameters (nm) | Lattice angles (°) | ||||
|---|---|---|---|---|---|---|---|
| a | b | c | |||||
| Monoclinic[7] | 4 | 0.850–0.868 | 0.487–0.508 | 0.922–0.974 | 92.8–94.5 | ||
| Triclinic [2]: 13 | 16 | 1.733 | 1.008 | 0.973 | 94.2 | 92.1 | 90.0 |
Mineralogical properties
edit| α | β | γ |
|---|---|---|
| 1.568 | 1.568 | 1.587 |
Etymology
editGibbsite is named after George Gibbs (1776–1833), an American mineral collector.[8]
References
edit- ^ Warr, L.N. (2021). "IMA–CNMNC approved mineral symbols". Mineralogical Magazine. 85 (3): 291–320. Bibcode:2021MinM...85..291W. doi:10.1180/mgm.2021.43. S2CID 235729616.
- ^ a b c d e f Wefers, Karl; Misra, Chanakya (1987). Oxides and hydroxides of aluminum. Alcoa Research Laboratories. OCLC 894928306.
- ^ N.N. Greenwood and A. Earnshaw, "Chemistry of Elements", 2nd edition, Butterworth and Heinemann, 1997
- ^ Saalfeld, H.; Wedde, M. (1974). "Refinement of the crystal structure of gibbsite, Al(OH)3" (PDF). Zeitschrift für Kristallographie. 139 (1–2): 129–135. Bibcode:1974ZK....139..129S. doi:10.1524/zkri.1974.139.1-2.129.
- ^ Gibbsite on Galleries.com
- ^ Advances in catalysis. Amsterdam. 24 November 2014. pp. 321–325. ISBN 978-0-12-800300-8. OCLC 894277485.
{{cite book}}: CS1 maint: location missing publisher (link) - ^ Gale, Julian D.; Rohl, Andrew L.; Milman, Victor; Warren, Michele C. (2001). "An ab Initio Study of the Structure and Properties of Aluminum Hydroxide: Gibbsite and Bayerite". The Journal of Physical Chemistry B. 105 (42): 10236–10242. doi:10.1021/jp011795e. ISSN 1520-6106.
- ^ Gibbsite Mineral Data on Webmineral.com
Further reading
edit- Hurlbut, Cornelius S.; Klein, Cornelis, 1985, Manual of Mineralogy, 20th ed., ISBN 0-471-80580-7