Aluminium hydroxide, Al(OH)3, is found in nature as the mineral gibbsite (also known as hydrargillite) and its three much rarer polymorphs: bayerite, doyleite, and nordstrandite. Aluminium hydroxide is amphoteric, i.e., it has both basic and acidic properties. Closely related are aluminium oxide hydroxide, AlO(OH), and aluminium oxide or alumina (Al2O3), the latter of which is also amphoteric. These compounds together are the major components of the aluminium orebauxite. Aluminium hydroxide also forms a gelatinous precipitate in water.
Al(OH)3 is built up of double layers of hydroxyl groups with aluminium ions occupying two-thirds of the octahedral holes between the two layers.[5][6] Four polymorphs are recognized.[7] All feature layers of octahedral aluminium hydroxide units, with hydrogen bonds between the layers. The polymorphs differ in terms of the stacking of the layers. All forms of Al(OH)3 crystals are hexagonal [disputed – discuss]:
Hydrargillite, once thought to be aluminium hydroxide, is an aluminium phosphate. Nonetheless, both gibbsite and hydrargillite refer to the same polymorphism of aluminium hydroxide, with gibbsite used most commonly in the United States and hydrargillite used more often in Europe. Hydrargillite is named after the Greek words for water (hydra) and clay (argylles).[citation needed]
In bases, it acts as a Lewis acid by binding hydroxide ions:[9]
Al(OH)3 + OH− → [Al(OH)4]−
Production
[edit]Red mud reservoirs (this one in Stade, Germany) contain the corrosive residues from the production of aluminium hydroxide.
Virtually all the aluminium hydroxide used commercially is manufactured by the Bayer process[10] which involves dissolving bauxite in sodium hydroxide at temperatures up to 270 °C (518 °F). The waste solid, bauxite tailings, is removed and aluminium hydroxide is precipitated from the remaining solution of sodium aluminate. This aluminium hydroxide can be converted to aluminium oxide or alumina by calcination.[citation needed]
The residue or bauxite tailings, which is mostly iron oxide, is highly caustic due to residual sodium hydroxide. It was historically stored in lagoons; this led to the Ajka alumina plant accident in 2010 in Hungary, where a dam bursting led to the drowning of nine people. An additional 122 sought treatment for chemical burns. The mud contaminated 40 square kilometres (15 sq mi) of land and reached the Danube. While the mud was considered non-toxic due to low levels of heavy metals, the associated slurry had a pH of 13.[11]
Aluminium hydroxide finds use as a fire retardant filler for polymer applications. It is selected for these applications because it is colorless (like most polymers), inexpensive, and has good fire retardant properties.[12]Magnesium hydroxide and mixtures of huntite and hydromagnesite are used similarly.[13][14][15][16][17] It decomposes at about 180 °C (356 °F), absorbing a considerable amount of heat in the process and giving off water vapour.
Freshly precipitated aluminium hydroxide forms gels, which are the basis for the application of aluminium salts as flocculants in water purification. This gel crystallizes with time. Aluminium hydroxide gels can be dehydrated (e.g. using water-miscible non-aqueous solvents like ethanol) to form an amorphous aluminium hydroxide powder, which is readily soluble in acids. Heating converts it to activated aluminas, which are used as desiccants, adsorbent in gas purification, and catalyst supports.[12]
Under the generic name "algeldrate", aluminium hydroxide is used as an antacid in humans and animals (mainly cats and dogs). It is preferred over other alternatives such as sodium bicarbonate because Al(OH)3, being insoluble, does not increase the pH of stomach above 7, and hence does not trigger secretion of excess acid by the stomach. Brand names include Alu-Cap, Aludrox, Gaviscon or Pepsamar. It reacts with excess acid in the stomach, reducing the acidity of the stomach content,[19][20] which may relieve the symptoms of ulcers, heartburnordyspepsia. Such products can cause constipation, because the aluminium ions inhibit the contractions of smooth muscle cells in the gastrointestinal tract, slowing peristalsis and lengthening the time needed for stool to pass through the colon.[21] Some such products are formulated to minimize such effects through the inclusion of equal concentrations of magnesium hydroxideormagnesium carbonate, which have counterbalancing laxative effects.[22]
This compound is also used to control hyperphosphatemia (elevated phosphate, or phosphorus, levels in the blood) in people and animals suffering from kidney failure. Normally, the kidneys filter excess phosphate out from the blood, but kidney failure can cause phosphate to accumulate. The aluminium salt, when ingested, binds to phosphate in the intestines and reduce the amount of phosphorus that can be absorbed.[23][24]
Precipitated aluminium hydroxide is included as an adjuvant in some vaccines (e.g. anthrax vaccine). One of the well-known brands of aluminium hydroxide adjuvant is Alhydrogel, made by Brenntag Biosector.[25][full citation needed][dead link] Since it absorbs protein well, it also functions to stabilize vaccines by preventing the proteins in the vaccine from precipitating or sticking to the walls of the container during storage. Aluminium hydroxide is sometimes called "alum", a term generally reserved for one of several sulfates.[citation needed]
Vaccine formulations containing aluminium hydroxide stimulate the immune system by inducing the release of uric acid, an immunological danger signal. This strongly attracts certain types of monocytes which differentiate into dendritic cells. The dendritic cells pick up the antigen, carry it to lymph nodes, and stimulate T cells and B cells.[26] It appears to contribute to induction of a good Th2 response, so is useful for immunizing against pathogens that are blocked by antibodies. However, it has little capacity to stimulate cellular (Th1) immune responses, important for protection against many pathogens,[27] nor is it useful when the antigen is peptide-based.[28]
In the 1960s and 1970s it was speculated that aluminium was related to various neurological disorders, including Alzheimer's disease.[29][30] Since then, multiple epidemiological studies have found no connection between exposure to environmental or swallowed aluminium and neurological disorders, though injected aluminium was not looked at in these studies.[31][32][33]
Neural disorders were found in experiments on mice motivated by Gulf War illness (GWI). Aluminium hydroxide injected in doses equivalent to those administered to the United States military, showed increased reactive astrocytes, increased apoptosis of motor neurons and microglial proliferation within the spinal cord and cortex.[34]
^Wells, A. F. (1975), Structural Inorganic Chemistry (4th ed.), Oxford: Clarendon Press
^ abEvans, K. A. (1993). "Properties and uses of aluminium oxides and aluminium hydroxides". In A. J. Downs (ed.). Chemistry of aluminium, gallium, indium, and thallium (1st ed.). London; New York: Blackie Academic & Professional. ISBN9780751401035.
^Hind, AR; Bhargava SK; Grocott SC (1999). "The Surface Chemistry of Bayer Process Solids: A Review". Colloids Surf Physiochem Eng Aspects. 146 (1–3): 359–74. doi:10.1016/S0927-7757(98)00798-5.
^Galbraith, A; Bullock, S; Manias, E; Hunt, B; Richards, A (1999). Fundamentals of pharmacology: a text for nurses and health professionals. Harlow: Pearson. p. 482.
^Papich, Mark G. (2007). "Aluminum Hydroxide and Aluminum Carbonate". Saunders Handbook of Veterinary Drugs (2nd ed.). St. Louis, Mo: Saunders/Elsevier. pp. 15–16. ISBN9781416028888.
^Washington, Neena (2 August 1991). Antacids and Anti Reflux Agents. Boca Raton, FL: CRC Press. p. 10. ISBN978-0-8493-5444-1.
^Plumb, Donald C. (2011). "Aluminum Hydroxide". Plumb's Veterinary Drug Handbook (7th ed.). Stockholm, Wisconsin; Ames, Iowa: Wiley. pp. 36–37. ISBN9780470959640.
^Lifelearn Inc. (1 November 2010). "Aluminum Hydroxide". Know Your Pet. Retrieved 30 June 2017.
