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Water beryllium

Beryllium Oxalate. BeryUium oxalate trihydrate [15771 -43-4], BeC204 -3H20, is obtained by evaporating a solution of beryUium hydroxide or oxide carbonate in a slight excess of oxaHc acid. The compound is very soluble in water. Beryllium oxalate is important for the preparation of ultrapure beryllium hydroxide by thermal decomposition above 320°C. The latter is frequentiy used as a standard for spectrographic analysis of beryUium compounds. [Pg.76]

Reflector Steel-water Steel-water Beryllium Steel-water Steel-water... [Pg.277]

Exposure to small amounts of beryllium occurs with ingestion of some foods and drinking water. Beryllium enters the air, water, and soil as a result of natural and human activities. Emissions from burning coal and oil increase beryllium levels in air. Beryllium enters waterways from the wearing away of rocks and soil. Most of the man-made beryllium that enters waterways comes when industry dumps waste water and when beryllium dust in the air from industrial activities settles over water Beryllium, as a chemical component, occurs naturally in soil however, disposal of coal ash, incinerator ash, and industrial wastes may increase the concentration of beryllium in soil. In air, beryllium compounds are present mostly as fine dust particles. The dust eventually settles over land and water. [Pg.266]

When the sample containing Be is fused with NaOH in a nickel crucible, and the cooled melt leached with water, beryllium remains in solution, while the insoluble residue contains Fe, Mn, Ni, Mg, Ti, and some other metal hydroxides. Traces of beryllium have been coprecipitated with Sn(OH)4 as collector, in the presence of EDTA at pH -13 [1]. [Pg.107]

Several compounds of beryllium have important applications. The most commercially important beryllium compound is beryllium oxide (BeO), which is used in high-temperature applications, such as crucibles, microwave ovens, ceramics, and insulators. Beryllium oxide also finds use in gyroscopes and military vehicle armor. Beryllium chloride (BeCl2) is used as a catalyst in the synthesis of organic chemicals. Beryllium hydride (BeH2) is a source of hydrogen gas when mixed with water. Beryllium carbide (Be2C) is a source of neutrons in nuclear reactors. [Pg.104]

The trend of increasing reactivity within the group is shown by the way the alkaline earth metals behave in the presence of water. Beryllium does not react with either water or steam, even when heated red-hot. Magnesium reacts slowly with liquid water and more readily with steam ... [Pg.272]

The lattice spacing is not a critical quantity in the second arrangement. Of course, the total amounts of heavy water, beryllium, and solvent must be kept in such limits as can be obtained from Table I. In addition, one will not want the neutron density in the moderator to exceed substantially the neutron density in the solution. If zero < 1, the neutron density at the tube wall will be less than 10% higher than the average neutron density in the tube. Since K =. 2 for both the Bi and the fluorocarbon solution of Table I, this only gives ro < 5 cm. The ratio of the neutron density difference between surface of cell and surface of tube, divided by the density at the tube is... [Pg.390]

After sintering and leaching out the sodium beryllium fluoride with water, beryllium hydroxide is precipitated by the addition of sodium hydroxide, i.e. [Pg.63]

How many collisions on the average are required with water, heavy water, beryllium, and uranium 238 to reduce neutron energy from 2 MeV to 1 eV ... [Pg.84]

Water. Beryllium is only slightly affected by H2O BeO and Be(OH)2 are insoluble in H2O. The basic carbonate is slightly soluble, the complex fluorides, e.g., Na2Bep4, moderately soluble. Salts (all very toxic) such as [Be(H20)4]S04 exemplify the tetrahedral [Be(H20)4]. ... [Pg.38]

The rapid fission of a mass of or another heavy nucleus is the principle of the atomic bomb, the energy liberated being the destructive power. For useful energy the reaction has to be moderated this is done in a reactor where moderators such as water, heavy water, graphite, beryllium, etc., reduce the number of neutrons and slow those present to the most useful energies. The heat produced in a reactor is removed by normal heat-exchange methods. The neutrons in a reactor may be used for the formation of new isotopes, e.g. the transuranic elements, further fissile materials ( °Pu from or of the... [Pg.44]

The alkali metals of Group I are found chiefly as the chlorides (in the earth s crust and in sea water), and also as sulphates and carbonates. Lithium occurs as the aluminatesilicate minerals, spodimene and lepidolite. Of the Group II metals (beryllium to barium) beryllium, the rarest, occurs as the aluminatesilicate, beryl-magnesium is found as the carbonate and (with calcium) as the double carbonate dolomite-, calcium, strontium and barium all occur as carbonates, calcium carbonate being very plentiful as limestone. [Pg.122]

The hydroxide of lithium, although soluble in water, is a weak base owing to the great attraction between the Li" and OH ions (p. 74) the hydroxide of beryllium is really a neutral, insoluble... [Pg.134]

These ion lasers are very inefficient, partly because energy is required first to ionize the atom and then to produce the population inversion. This inefficiency leads to a serious problem of heat dissipation, which is partly solved by using a plasma tube, in which a low-voltage high-current discharge is created in the Ar or Kr gas, made from beryllium oxide, BeO, which is an efficient heat conductor. Water cooling of the tube is also necessary. [Pg.354]

Beryllium Hydride. BeryUium hydride [13597-97-2] is an amorphous, colorless, highly toxic polymeric soHd (H = 18.3%) that is stable to water but hydroly2ed by acid (8). It is insoluble in organic solvents but reacts with tertiary amines at 160°C to form stable adducts, eg, (R3N-BeH2 )2 (9). It is prepared by continuous thermal decomposition of a di-/-butylberylhum-ethyl ether complex in a boiling hydrocarbon (10). [Pg.299]

Beryllium has a high x-ray permeabiUty approximately seventeen times greater than that of aluminum. Natural beryUium contains 100% of the Be isotope. The principal isotopes and respective half-life are Be, 0.4 s Be, 53 d Be, 10 5 Be, stable Be, 2.5 x 10 yr. Beryllium can serve as a neutron source through either the (Oi,n) or (n,2n) reactions. Beryllium has alow (9 x 10 ° m°) absorption cross-section and a high (6 x 10 ° m°) scatter cross-section for thermal neutrons making it useful as a moderator and reflector in nuclear reactors (qv). Such appHcation has been limited, however, because of gas-producing reactions and the reactivity of beryUium toward high temperature water. [Pg.66]

Beryllium fluoride is hygroscopic and highly soluble in water, although its dissolution rate is slow. FluoroberyUates can be readily prepared by crystallization or precipitation from aqueous solution. Compounds containing the BeP ion are the most readily obtained, though compounds containing other fluoroberyUate ions can also be obtained, eg, NH BeF, depending upon conditions. [Pg.75]

BeryUium chloride [7787-47-5], BeCl2, is prepared by heating a mixture of beryUium oxide and carbon in chloride at 600—800°C. At pressures of 2.7—6.7 Pa (0.02—0.05 mm Hg) beryllium chloride sublimes at 350—380°C. It is easily hydrolyzed by water vapor or in aqueous solutions. BeryUium chloride hydrate [14871-75-1] has been obtained by concentrating a saturated aqueous solution of the chloride in a stream of hydrogen chloride. ChloroberyUate compounds have not been isolated from aqueous solutions, but they have been isolated from anhydrous fused salt mixtures. [Pg.75]

Beryllium Nitrate. BeryUium nitrate tetrahydrate [13516-48-0], Be(N02)2 4H2O, is prepared by crystallization from a solution of beryUium hydroxide or beryllium oxide carbonate in a slight excess of dilute nitric acid. After dissolution is complete, the solution is poured into plastic bags and cooled to room temperature. The crystallization is started by seeding. Crystallization from more concentrated acids yields crystals with less water of hydration. On heating above 100°C, beryllium nitrate decomposes with simultaneous loss of water and oxides of nitrogen. Decomposition is complete above 250°C. [Pg.76]

Beryllium potassium fluoride [7787-50-0] M 105.1. Crystd from hot water (25mL/g). [Pg.400]


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See also in sourсe #XX -- [ Pg.59 , Pg.60 ]




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