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Beryllium ceramic production

Heating the ammonium beryllium carbonate solution to 95°C causes nearly quantitative precipitation of beryllium basic carbonate [66104-24-3], Be(OH)2 2BeC03. Evolved carbon dioxide and ammonia are recovered for recycle as the strip solution. Continued heating of the beryllium basic carbonate slurry to 165°C liberates the remaining carbon dioxide and the resulting beryllium hydroxide [13327-32-7] intermediate is recovered by filtration. The hydroxide is the basic raw material for processing into beryllium metal, copper—beryllium and other alloys, and beryllia [1304-56-9] for ceramic products. Approximately 90% of the beryllium content of bertrandite is recovered by this process. [Pg.67]

Beryllium oxide ceramics exhibit the highest thermal conductivity of all the ceramic products and are the best electrical insulators at high temperatures. Despite these exceptional properties, beryllium oxide ceramics have only found limited application due to their high cost and poisonousness. They are manufactured by sintering dry or plastically pressed fine particulate beryllium oxide at 1400 to 1450°C in a hydrogen atmosphere. [Pg.462]

The aqueous beryllium sulfate is separated from the solids by counter-current decantation thickener operations. A beryllium concentrate is produced by a counter-current solvent extraction process (Maddox and Foos 1966). This concentrate is stripped of its beryllium content with aqueous ammonium carbonate. By heating to 70 °C, aluminum and iron are precipitated and then removed by filtration. Precipitation of beryllium basic carbonate occurs when the solution is heated to 95 °C. The carbonate is filtered, deionized water is added, and heating to 165 °C yields a beryllium hydroxide product which is the common input to beryllium-copper alloy, beryllium oxide ceramics, or pure beryllium metal (Table 2.1-2). [Pg.577]

A rapid development of certain specialized industries such as the production of computers, beryllium ceramics, nuclear power engineering, rocket techniques and other complex technologies give rise to the possibility of occupational exposure to beryllium effects. In the vicinity of works producing beryllium, its alloys or salts, and also in coal combustion (where as much as 100 g of beryllium may be present in one ton of certain types of coal), the atmosphere is polluted with this toxic element, which thus leads to the exposure of the population in these localities. The maximal permissible beryllium concentration is as low as 0.002 mg m. ... [Pg.799]

Beryllium, beryllium-containing aUoys, and beryUium oxide ceramic in soHd or massive form present no hazard whatsoever (31). SoHd shapes may be safely handled with bare hands (32) however, care must be taken in the fabrication and processing of beryUium products to avoid inhalation of airborne beryUium particulate matter such as dusts, mists, or fumes in excess of the prescribed workplace exposure limits. Inhalation of fine airborne beryUium may cause chronic beryUium disease, a serious lung disease in certain sensitive individuals. However, the vast majority of people, perhaps as many as 99%, do not react to beryUium exposure at any level (33). The biomedical and environmental aspects of beryUium have been summarized (34). [Pg.69]

Beryllium Sulfate. BeiyUium sulfate tetiahydiate [7787-56-6], BeSO TH O, is produced commeicially in a highly purified state by fiactional crystallization from a berylhum sulfate solution obtained by the reaction of berylhum hydroxide and sulfuric acid. The salt is used primarily for the production of berylhum oxide powder for ceramics. Berylhum sulfate chhydrate [14215-00-0], is obtained by heating the tetrahydrate at 92°C. Anhydrous berylhum sulfate [13510-49-1] results on heating the chbydrate in air to 400°C. Decomposition to BeO starts at about 650°C, the rate is accelerated by heating up to 1450°C. At 750°C the vapor pressure of SO over BeSO is 48.7 kPa (365 mm Hg). [Pg.77]

Feldspar [68476-25-5] - [CERAMICS - OVERVIEW] (Vol 5) - [ALUMINUMCOMPOUNDS - INTRODUCTION] (Vol2) - [CLAYS - USES] (Vol 6) - [BARIUMCOMPOUNDS] (Vol3) - [ENAMELS, PORCELAIN ORVITREOUS] (Vol 9) -as abrasive [ABRASIVES] (Vol 1) -beryl as by-product [BERYLLIUM AND BERYLLIUM ALLOYS] (Vol 4)... [Pg.394]

Beryllium is used commercially in three major forms as a pure metal, as an alloy with other metals, and as a ceramic. The favorable mechanical properties of beryllium, e.g., its specific stiffness, have made it a major component for certain aerospace applications in satellites and spacecraft. As a modulator and reflector of neutrons, beryllium is of interest in fusion reactions and for nuclear devices that have defense applications. When a small amount of beryllium is added to copper, the desirable properties of copper (i.e., thermal and electrical conductivity) are kept but the material is considerably stronger. The superior thermal conductivity of beryllium oxide ceramics has made the product useful for circuit boards and laser tubes. A more complete discussion of the applications of beryllium was recently reviewed [2]. [Pg.261]

Beryllium oxide A compound commonly used in the production of ceramics for electrical applications and whose dust or fumes are toxic. [Pg.2337]

After working with beryllium I moved on to study nuclear reactor fabrication. In this study I worked on determining the surface area, size and shape distributions of uranium dioxide and plutonium dioxide powders used to fabricate fuel rods. Looking back I see that my initiation into powder technology was a baptism of fire since all of these powders were extremely toxic and dangerous. The technology that I studied in those years is currently very applicable to the study of modern ceramic materials and powder metallurgical routes to finished products [1,2]. [Pg.1]


See other pages where Beryllium ceramic production is mentioned: [Pg.196]    [Pg.289]    [Pg.58]    [Pg.96]    [Pg.71]    [Pg.34]    [Pg.249]    [Pg.265]    [Pg.379]    [Pg.54]    [Pg.33]    [Pg.109]   
See also in sourсe #XX -- [ Pg.577 , Pg.578 ]




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