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14-1389: Borate ions occur, alone or with other anions, in many borate and borosilicate minerals such as borax , boracite , ulexite (boronatrocalcite) and colemanite . Borates also occur in seawater, where they make an important contribution to the absorption of low frequency sound in seawater. Borates also occur in plants, including almost all fruits. The main borate anions are: In 1905, Burgess and Holt observed that fusing mixtures of boric oxide B 2 O 3 and sodium carbonate Na 2 CO 3 yielded on cooling two crystalline compounds with definite compositions, consistent with anhydrous borax Na 2 B 4 O 7 (which can be written Na 2 O·2B 2 O 3 ) and sodium octaborate Na 2 B 8 O 13 (which can be written Na 2 O·4B 2 O 3 ). Borate anions (and functional groups) consist of trigonal planar BO 3 and/or tetrahedral BO 4 structural units, joined together via shared oxygen atoms (corners) or atom pairs (edges) into larger clusters so as to construct various ions such as [B 2 O 5 ] , [B 3 O 8 ] , [B 4 O 12 ] , [B 5 O 6 (OH) 5 ] , [B 6 O 13 ] , etc. These anions may be cyclic or linear in structure, and can further polymerize into infinite chains, layers, and tridimensional frameworks. The terminal (unshared) oxygen atoms in

28-473: A silicate in which some [SiO 4 ] units are replaced by [BO 4 ] centers, together with additional cations to compensate for the difference in valence states of Si(IV) and B(III). Because this substitution leads to imperfections, the material is slow to crystallise and forms a glass with low coefficient of thermal expansion , thus resistant to cracking when heated, unlike soda glass . Common borate salts include sodium metaborate (NaBO 2 ) and borax. Borax

42-494: A wood preservative or fungicide. Zinc borate is used as a flame retardant . Some borates with large anions and multiple cations, like K 2 Al 2 B 2 O 7 and Cs 3 Zn 6 B 9 O 21 have been considered for applications in nonlinear optics . Borate esters are organic compounds , which are conveniently prepared by the stoichiometric condensation reaction of boric acid with alcohols (or their chalcogen analogs). Metal borate thin films have been grown by

56-947: A mixture of B(OH) 3 , [B(OH) 4 ] , [B 3 O 3 (OH) 4 ] , and [B 5 O 6 (OH) 4 ] . These ions, similarly to the complexed borates mentioned above, are more acidic than boric acid itself. As a result of this, the pH of a concentrated polyborate solution will increase more than expected when diluted with water. A number of metal borates are known. They can be obtained by treating boric acid or boron oxides with metal oxides. Some chemicals contain another anion in addition to borate. These include borate chlorides , borate carbonates , borate nitrates , borate sulfates , borate phosphates . More complex anions can be formed by condensing borate triangles or tetrahedra with other oxyanions to yield materials such as borosulfates , boroselenates , borotellurates , boroantimonates , borophosphates , or boroselenites . Borosilicate glass , also known as pyrex , can be viewed as

70-401: A mixture of both, can be used in borate fusion sample preparation of various samples for analysis by XRF , AAS , ICP-OES and ICP-MS . Borate fusion and energy dispersive X-ray fluorescence spectrometry with polarized excitation have been used in the analysis of contaminated soils. Disodium octaborate tetrahydrate Na 2 B 8 O 13 ·4H 2 O (commonly abbreviated DOT) is used as

84-546: A variety of techniques, including liquid-phase epitaxy (e.g. FeBO 3 , β-BaB 2 O 4 ), electron-beam evaporation (e.g. CrBO 3 , β-BaB 2 O 4 ), pulsed laser deposition (e.g. β-BaB 2 O 4 ,  Eu(BO 2 ) 3 ), and atomic layer deposition (ALD). Growth by ALD was achieved using precursors composed of the tris(pyrazolyl)borate ligand and either ozone or water as the oxidant to deposit CaB 2 O 4 , SrB 2 O 4 , BaB 2 O 4 , Mn 3 (BO 3 ) 2 , and CoB 2 O 4 films. Borate anions are largely in

98-401: A weak Brønsted acid , that is, a proton donor, with p K a ~ 9 . However, it more often acts as a Lewis acid , accepting an electron pair from a hydroxide ion produced by the water autoprotolysis : This reaction is very fast, with characteristic time less than 10 μs . Polymeric boron oxoanions are formed in aqueous solution of boric acid at pH 7–10 if the boron concentration

112-523: Is higher than about 0.025 mol/L. The best known of these is the tetraborate ion [B 4 O 7 ] , found in the mineral borax: Other anions observed in solution are triborate(1−) and pentaborate(1−), in equilibrium with boric acid and tetrahydroxyborate according to the following overall reactions: In the pH range 6.8 to 8.0, any alkali salts of "boric oxide" anions with general formula [B x O y (OH) z ](( q ) where 3 x + q = 2 y + z will eventually equilibrate in solution to

126-824: Is severely abraded. It distributes throughout the body and is not retained in tissues, except for bone, and is rapidly excreted in the urine. Borate mineral The Borate Minerals are minerals which contain a borate anion group. The borate (BO 3 ) units may be polymerised similar to the SiO 4 unit of the silicate mineral class. This results in B 2 O 5 , B 3 O 6 , B 2 O 4 anions as well as more complex structures which include hydroxide or halogen anions. The [B(O,OH) 4 ] anion exists as well. Many borate minerals, such as borax , colemanite , and ulexite , are salts : soft, readily soluble, and found in evaporite contexts. However, some, such as boracite , are hard and resistant to weathering, more similar to

140-578: Is soluble in water, so mineral deposits only occur in places with very low rainfall. Extensive deposits were found in Death Valley and shipped with twenty-mule teams from 1883 to 1889. In 1925, deposits were found at Boron , California on the edge of the Mojave Desert . The Atacama Desert in Chile also contains mineable borate concentrations. Lithium metaborate , lithium tetraborate, or

154-521: The silicates . There are over 100 different borate minerals. Borate minerals include: IMA -CNMNC proposes a new hierarchical scheme (Mills et al., 2009). This list uses it to modify the Classification of Nickel–Strunz ( mindat.org , 10 ed, pending publication). Note that although Nickel–Strunz division letters were traditionally based on the number of boron atoms in a mineral's chemical formula (06.A are monoborates, 06.B are diborates, etc.),

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168-711: The borate anions may be capped with hydrogen atoms ( −OH ) or may carry a negative charge ( −O ). The planar BO 3 units may be stacked in the crystal lattice so as to have π-conjugated molecular orbitals , which often results in useful optical properties such as strong harmonics generation, birefringence , and UV transmission . Polymeric borate anions may have linear chains of 2, 3 or 4 trigonal BO 3 structural units, each sharing oxygen atoms with adjacent unit(s). as in LiBO 2 , contain chains of trigonal BO 3 structural units. Other anions contain cycles; for instance, NaBO 2 and KBO 2 contain

182-585: The cyclic [B 3 O 6 ] ion, consisting of a six-membered ring of alternating boron and oxygen atoms with one extra oxygen atom attached to each boron atom. The thermal expansion of crystalline borates is dominated by the fact that BO 3 and BO 4 polyhedra and rigid groups consisting of these polyhedra practically do not change their configuration and size upon heating, but sometimes rotate like hinges, which results in greatly anisotropic thermal expansion including linear negative expansion. In aqueous solution, boric acid B(OH) 3 can act as

196-462: The form of the undissociated acid in aqueous solution at physiological pH. No further metabolism occurs in either animals or plants. In animals, boric acid/borate salts are essentially completely absorbed following oral ingestion. Absorption occurs via inhalation, although quantitative data are unavailable. Limited data indicate that boric acid/salts are not absorbed through intact skin to any significant extent, although absorption occurs through skin that

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