| 词条 | Gibbsite |
| 释义 |
| name = Gibbsite | boxwidth = | boxbgcolor = | image = Gibbsite-fiu14a.jpg | imagesize = | alt = | caption = Gibbsite from China | category = Hydroxide minerals | formula = Al(OH)3 | molweight = | strunz = 4.FE.10 | dana = | system = Monoclinic | class = Prismatic (2/m) (same H-M symbol) | symmetry = P21/m | unit cell = | color = | colour = | habit = | twinning = | cleavage = | fracture = | tenacity = | mohs = 2.5-3 | luster = | streak = | diaphaneity = | gravity = 2.35 | density = | polish = | opticalprop = | refractive = | birefringence = | pleochroism = | 2V = | dispersion = | extinction = | length fast/slow = | fluorescence = | absorption = | melt = | fusibility = | diagnostic = | solubility = | impurities = | alteration = | other = | prop1 = | prop1text = | references = }} Gibbsite, Al(OH)3, is one of the mineral forms of aluminium hydroxide. It is often designated as γ-Al(OH)3 (but sometimes as α-Al(OH)3.[1]). It is also sometimes called hydrargillite (or hydrargyllite). 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, but sometimes as β-Al(OH)3), doyleite, and nordstrandite. Gibbsite and bayerite are monoclinic, whereas doyleite and nordstrandite are triclinic forms.{{Citation needed|date=January 2013}} StructureThe structure of gibbsite is interesting and analogous to the basic structure of the micas. The basic structure forms stacked sheets of linked octahedrons of aluminium hydroxide. The octahedrons are composed of aluminium ions with a +3 charge bonded to six octahedrally coordinated hydroxides with a -1 charge. Each of the hydroxides is bonded to only two aluminium atoms because one third of the octahedrons are vacant a central aluminium. The result is a neutral sheet since +3/6 = +1/2 (+3 charge on the aluminiums divided by six hydroxide bonds times the number of aluminiums) and -1/2 = -1/2 (-1 charge on the hydroxides divided between only two aluminiums); thus the charges cancel. 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|date=January 2013}} 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.[2] EtymologyGibbsite is named after George Gibbs (1776–1833), an American mineral collector.[3] References1. ^N.N. Greenwood and A. Earnshaw, "Chemistry of Elements", 2nd edition, Butterworth and Heinemann, 1997 2. ^GIBBSITE (Aluminum Hydroxide) 3. ^Gibbsite Mineral Data Further reading
External links{{commons category|Gibbsite}}
4 : Aluminium minerals|Hydroxide minerals|Monoclinic minerals|Luminescent minerals |
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