Alkaline earth metal boronates

Beddoes — Rumford — The Royal Institution — Davy — Works — Phosoxygen — Nitrous Oxide — Tanning Agricultural Chemistry — Galvanism — The Alkali Metals — The Alkaline Earth Metals — Boron — Chlorine — Nitrogen Chloride — Fluorine — Phosphorus Compounds — Atomic Weights — Various Researches — Researches on Flame — Electrical Researches — John Davy — Edmimd Davy — Brande — Silliman. 

Chemical Properties. In addition to the reactions Hsted in Table 3, boron trifluoride reacts with alkali or alkaline-earth metal oxides, as well as other inorganic alkaline materials, at 450°C to yield the trimer trifluoroboroxine [13703-95-2] (BOF), MBF, and MF (29) where M is a univalent metal ion. The trimer is stable below — 135°C but disproportionates to B2O2 and BF at higher temperatures (30). 

Boron tnhahdes can be reduced to elemental boron by heating and presence of alkah metals, alkaline-earth metals, or (22—26) such reductions... 

Electrons are not only charged, they also have a characteristic physicists call spin. Pairing two electrons by spin, which has two possible values, up or down, confers additional stability. Bei yllium (Be, atomic number 4) has two spin-paired electrons in its second shell that are easily given up in chemical reactions. Beryllium shares this characteristic with other elements in column two, the alkaline earth metals. These atoms also generally form ionic bonds. Boron... 

Ca3(BN2)2 is readily formed when (distilled) calcium metal is melted in the presence of (layer-type) boron nitride. This reaction provides some insight on how alkaline-earth metals like calcium may act as a catalyst in the phase transformation of layered a-BN into its cubic modification. Instead of metals, nowadays alkaline-earth (Ca, Sr, Ba) nitridoborates can be used as a flux catalyst in high-pressure and high-temperature transformation reactions to produce cubic boron nitride [15]. 

Chemical effects include stable compound formation and ionization, both of which decrease the population of free atoms in the sample vapour and thereby lower the measured absorbance. Examples of compound formation include reactions between alkaline earth metals and oxyanions such as aluminates, silicates and phosphates, as well as the formation of stable oxides of aluminium, vanadium, boron etc. 

Sir Humphry Davy, 1778-1829. British chemist who isolated the alkali and alkaline earth metals and boron, and proved that chlorine is an element. Gay-Lussac and Thenard isolated boron independently at about the same time. 

The formation of a metal structure from free atoms must be associated with ionization, from which it follows that a high ionization energy in an element prevents it. Metallic properties are therefore found in the alkali- and alkaline-earth elements. Boron, the first element in the third group, is hardly metallic in this group the element with the smallest ionic radius loses its metallic character. 

The interaction between sodium and alkaline-earth metal ions and borate has attracted recent attention, particularly from the point of view of association of ions in seawater. Several studies (69, 114,168, 169, 340) have shown that the boron content of seawater (4-5 x 10 4 M) is too low to support appreciable concentrations of polyborate species. The increase in acidity of boric acid in the presence of metal ions results from ion-pair formation ... 

The relationship between the composition and structure of borates and their decomposition in aqueous solution has been reviewed (78, 226,414,417). Borates of the alkali and alkaline-earth metals give an alkaline reaction in solution, as the borates formed by hydrolysis possess a lower boron-to-metal ratio than in the initial material (414). 

Most chalcophile elements (i.e, S and other elements with an affinity for S in nature such as Cu, As, Se, Cd, In, and W), boron, and the halogens are enriched in coal with respect to soil, and this accounts in part for their enrichment in emitted particles. Differences between eastern and western coals are apparent for many elements, especially the alkali and alkaline earth metals, As, and In. This accounts for some of the large plant-to-plant variability that we observe below. 

The characteristics of this group are that the elements possess a valence of 3, and that the oxides, M2O3, have but a weakly developed basic character. Boron, in fact, shows practically no base-forming properties, but forms rather a weak acid. The oxide of aluminum displays both basic and acidic properties that is, it is amphoteric. The remaining elements are more distinctly base-forming than aluminum, without, however, approaching in any way the alkaline earth metals in this respect. 

The tetrahydroborate salts of alkali metals, M[BH4] (M = Li, Na, K),1 are important because they serve as starting materials for the preparation of other boron hydrides2,3 and because they are used frequently as reducing agents.4 The lithium and sodium salts are prepared on a technical scale.5 9 The tetrahydroborate salts of the alkaline earth metals, M[BH4]2 (M = Mg, Ca, Sr, Ba), have not as yet been used extensively however, calcium bis[tetrahydroborate(l-)], Ca(BH4)2,10 is very soluble in tetrahydrofuran (THF) and it therefore has considerable potential application as a substitute for the lithium and sodium salts. 

Rednction of boron trihaUdes to elemental boron can be accomplished by heating with alkali metals, alkaline earth metals, or hydrogen. Under the proper conditions, rednctions of this type can also yield diborane and, under selected conditions, boron subhalides (see below). Metal hydrides also react with boron trihalides to give diborane. Boron nitride and boron carbide have been prepared by the high-temperature reductions of boron trihalides with ammonia and methane, respectively, and deposited on metal substrates by CVD. 

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