Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Sulfate insoluble barium

Quantitatively, sulfur in a free or combined state is generally determined by oxidizing it to a soluble sulfate, by fusion with an alkaH carbonate if necessary, and precipitating it as insoluble barium sulfate. Oxidation can be effected with such agents as concentrated or fuming nitric acid, bromine, sodium peroxide, potassium nitrate, or potassium chlorate. Free sulfur is normally determined by solution in carbon disulfide, the latter being distilled from the extract. This method is not useful if the sample contains polymeric sulfur. [Pg.124]

In metallic form, barium is very reactive, reacting readily with water to release hydrogen. In aqueous solution it is present as an ion with a +2 charge. Barium acetate, chloride, hydroxide, and nitrate are water-soluble, whereas barium arsenate, chromate, duoride, oxalate, and sulfate are not. Most water-insoluble barium salts dissolve in dilute acids barium sulfate, however, requkes strong sulfuric acid. [Pg.475]

Water-insoluble barium salts are poorly absorbed. In fact, barium sulfate is used as a contrast material for x-ray examination of the gastrointestinal tract based on its limited solubility andlow toxicity (52). Barium sulfate fed to mice at various levels up to 8 ppm dietary Ba ( 1.14 mg/kg-d as Ba " ) for three generations had no significant effects on growth, mortality, morbidity, or reproductive performance (53). [Pg.483]

In humans, inhaled insoluble barium salts are retained in the lung (47,49). Inhalation of high concentrations of the fine dusts of barium sulfate can result in the formation of harmless nodular granules in the lungs, a condition called baritosis (49). Baritosis produces no specific symptoms and no changes in pulmonary function. The nodulates disappear upon cessation of exposure to the barium salt. However, it is possible that barium sulfate may produce benign pneumoconiosis because, unlike barium carbonate, barium sulfate is poorly absorbed (21). [Pg.483]

The classical analytical method of deterruination of barium ion is gravimetric, by precipitating and weighing insoluble barium sulfate. Barium chromate, which is more insoluble than strontium chromate in a slightly acidic solution, gives a fairly good separation of the two elements. [Pg.484]

This equation may be interpreted to mean that any soluble barium salt will react with any soluble sulfate to produce (insoluble) barium sulfate. [Pg.153]

Compounds Soluble—barium nitrate, barium sulfide, barium chloride, barium hydroxide, barium acetate insoluble—barium sulfate... [Pg.65]

Impurities such as heavy metal sulfides are filtered out. Water-soluble sulfur compounds are oxidized to insoluble barium sulfate and removed. The solution is then evaporated to crystaUize barium chloride. [Pg.84]

Barium hydroxide decomposes to barium oxide when heated to 800°C. Reaction with carbon dioxide gives barium carbonate. Its aqueous solution, being highly alkahne, undergoes neutrahzation reactions with acids. Thus, it forms barium sulfate and barium phosphate with sulfuric and phosphoric acids, respectively. Reaction with hydrogen sulfide produces barium sulfide. Precipitation of many insoluble, or less soluble barium salts, may result from double decomposition reaction when Ba(OH)2 aqueous solution is mixed with many solutions of other metal salts. [Pg.87]

In an atmosphere of nitric oxide, thermal decomposition produces barium nitrite, Ba(N02)2. Reactions with soluble metal sulfates or sulfuric acid yield barium sulfate. Many insoluble barium salts, such as the carbonate, oxalate and phosphate of the metal, are precipitated by similar double decomposition reactions. Ba(N03)2 is an oxidizer and reacts vigorously with common reducing agents. The solid powder, when mixed with many other metals such as aluminum or zinc in their finely divided form, or combined with alloys such as... [Pg.88]

Uranium mineral first is digested with hot nitric acid. AH uranium and radium compounds dissolve in the acid. The solution is filtered to separate insoluble residues. The acid extract is then treated with sulfate ions to separate radium sulfate, which is co-precipitated with the sulfates of barium, strontium, calcium, and lead. The precipitate is boiled in an aqueous solution of sodium chloride or sodium hydroxide to form water-soluble salts. The solution is filtered and the residue containing radium is washed with boiling water. This residue also contains sulfates of other alkahne earth metals. The sohd sulfate mixture of radium and other alkahne earth metals is fused with sodium carbonate to convert these metals into carbonates. Treatment with hydrochloric acid converts radium and other carbonates into chlorides, all of which are water-soluble. Radium is separated from this solution as its chloride salt by fractional crystallization. Much of the barium, chemically similar to radium, is removed at this stage. Final separation is carried out by treating radium chloride with hydrobromic acid and isolating the bromide by fractional crystallization. [Pg.785]

Rubidium is recovered from its ore lepidolite or pollucite. Mineral lepidolite is a lithium mica having a composition KRbLi(OH,F)Al2Si30io. The ore is opened by fusion with gypsum (potassium sulfate) or with a mixture of barium sulfate and barium carbonate. The fused mass is extracted with hot water to leach out water-soluble alums of cesium, rubidium, and potassium. The solution is filtered to remove insoluble residues. Alums of alkali metals are separated from solution by fractional crystallization. Solubility of rubidium alum or rubidium aluminum sulfate dodecahydrate, RbAl(S04)2 I2H2O falls between potassium and cesium alum. [Pg.796]

Rubidium hydroxide may be obtained as an intermediate in recovering rubidium metal from mineral lepidohte (see Rubidium). In the laboratory it may be prepared by adding barium hydroxide to a solution of rubidium sulfate. The insoluble barium sulfate is separated by filtration ... [Pg.800]

Rubidium acid salts are usually prepared from rubidium carbonate or hydroxide and the appropriate acid in aqueous solution, followed by precipitation of the crystals or evaporation to dryness. Rubidium sulfate is also prepared by the addition of a hot solution of barium hydroxide to a boiling solution of rubidium alum until all the aluminum is precipitated. The pH of the solution is 7.6 when the reaction is complete. Aluminum hydroxide and barium sulfate are removed by filtration, and rubidium sulfate is obtained by concentration and crystallization from the filtrate. Rubidium aluminum sulfate dodecahydrate [7488-54-2] (alum), RbA SO 12H20, is formed by sulfuric acid leaching of lepidolite ore. Rubidium alum is more soluble than cesium alum and less soluble than the other alkali alums. Fractional crystallization of Rb alum removes K, Na, and Li values, but concentrates the cesium value. Rubidium hydroxide, RbOH, is prepared by the reaction of rubidium sulfate and barium hydroxide in solution. The insoluble barium sulfate is removed by filtration. The solution of rubidium hydroxide can be evaporated partially in pure nickel or silver containers. Rubidium hydroxide is usually supplied as a 50% aqueous solution. Rubidium carbonate, Rb2C03, is readily formed by bubbling carbon dioxide through a solution of rubidium hydroxide, followed by evaporation to dryness in a fluorocarbon container. Other rubidium compounds can be formed in the laboratory by means of anion-exchange techniques. Table 4 lists some properties of common rubidium compounds. [Pg.280]

Barium ferrate, BaFe04, like barium sulfate and barium chromate, is insoluble and is the most stable of the ferrates. Dissolve the potassium salt in about ten times its weight of water, filter it through a filter paper... [Pg.95]

Chemically related to barium, radium is recovered from its ores by addition of barium salt, followed by treatment as fur recovery of barium, usually as the sulfate. The sulfates of barium and of radium are insoluble in most chemicals, so they arc transformed into carbonate or sulfide, both of which are readily soluble in HC1. Separation from barium is accomplished by fractional crystallization of the chlorides (or bromides, or hydroxides). Dry, concentrated radium salts are preserved in sealed glass tubes, which are periodically opened by experienced workers to relieve the pressure, The glass tubes are kept m lead shields,... [Pg.1417]

Analytical Methods. Insoluble barium sulfate precipitate, one of the two criteria by which growth of the bacteria was established was determined by standard gravimetric methods. The amount of barium sulfate is directly proportional to the amount of sulfide that has been oxidized by the sulfur bacteria. [Pg.144]

Precipitation of insoluble sulfates of barium, lead and calcium. [Pg.270]

Barium chloride Sulfates, S042- White precipitate of barium sulfate insoluble in warm dilute hydrochloric acid and in dilute nitric acid slightly soluble in boiling hydrochloric acid... [Pg.534]

Zinc oxide (ZnO), which is produced by burning zinc vapor in atmospheric oxygen, is by far the most important compound of zinc. Under the name of zinc white, the oxide is used as a paint pigment. It is also used as a base in the manufacture of enamels and glass, and as a ruler in the fabrication of automobile tires and other kinds of rubber goods. Zinc sulfide (ZnS) is also an important white paint pigment which is used either as such or in the form of lithopone, which is a mixture of zinc sulfide and barium sulfate. This widely used pigment is prepared by the metathetical reaction between zinc sulfate and barium sulfide, a reaction in which both of the products are insoluble ... [Pg.563]

Numerous factors may be involved with the toxic substance itself. If the substance is a toxic heavy metal cation, the nature of the anion with which it is associated can be crucial. For example, barium ion, Ba2+, in the form of insoluble barium sulfate, BaS04, is routinely used as an x-ray opaque agent in the gastrointestinal tract for diagnostic purposes (barium enema x-ray). This is a safe procedure however, soluble barium salts such as BaCl2 are deadly poisons when introduced into the gastrointestinal tract. [Pg.137]

When evaluating the health effects of barium compounds, it is important to keep in mind that different barium compounds have different solubilities in water and body fluids and therefore serve as variable sources of the Ba + ion. The Ba + ion and the soluble compounds of barium (notably chloride, nitrate, hydroxide) are generally highly toxic to humans and experimental animals. The insoluble barium compounds (notably sulfate and carbonate) are inefficient sources of the Ba + ion and therefore are generally nontoxic. Throughout the following section (2.2), the health effects by route of exposure of both soluble and insoluble barium compounds are discussed. [Pg.15]

The first chemical work on calabash curare was carried out in 1897 by Boehm (8), who isolated a highly active amorphous material which was named curarine. This was soluble in water and insoluble in ether, so it is probable that Boehm was handling a mixture of crude quaternary alkaloids. Much later (1935), King described (9) the preparation of an equally active amorphous quaternary iodide from the bark of S. toxifera. However, the first isolation of well-characterized crystalline alkaloids was achieved by H. Wieland and his school (10-13). Calabash curares were extracted with methanol, and the water-soluble quaternary alkaloids in the extract were precipitated as the reineckate salts this mixture was then fractionated by adsorption chromatography on alumina. The various reineckate fractions so obtained were converted into the corresponding chlorides by successive treatment with equivalent quantities of silver sulfate and barium chloride some of the quaternary alkaloids then crystallized as the chlorides or as the picrates. C-Curarine1... [Pg.517]

In the gastrointestinal tract the insoluble barium sulfate is still most commonly used, but water-soluble iodi-nated media can be used in special circumstances. [Pg.1849]

For the reaction of potassium sulfate with barium nitrate, the net ionic equation shows that aqueous barium and sulfate ions join to form solid, insoluble barium sulfate. [Pg.305]

The light areas on this X ray of the digestive tract show insoluble barium sulfate. [Pg.535]

Addition of sodium sulfate as a lavage solution may precipitate the very insoluble barium sulfate. As potassium deficiency occurs in acute poisoning, serum potassium and cardiac rhythm must be monitored closely. Administration of intravenous potassium appears beneficial. As renal failure is also a concern, urinary output also must be monitored closely. [Pg.214]

In an aqueous solution, ionic compounds are completely dissociated into ions. For example, an aqueous solution of barium nitrate, Ba(N03)2, contains Ba + ions and NO3 ions. If aqueous solutions of ionic compounds are mixed, some ions may interact to form an insoluble product called a precipitate. For example, if aqueous solutions of barium nitrate and sodium sulfate are mixed, insoluble barium sulfate will precipitate. The complete formula equation for this reaction is written as follows. [Pg.456]

Barium is probably best known in the form of barium sulfate (BaS04). Barium sulfate is a white solid that is insoluble in the human gastrointestinal (GI) tract. It is administered in powdered form as a contrast agent for use in X-ray pictures of the upper and lower GI tracts. Any abnormal growths—cancerous tumors, for example—will clearly show as dark spots in the X-rays against the white background of the BaSCf. [Pg.132]

Side reactions of barium with silicate impurities in the ore have been noted (1,11—13). These reactions can cause appreciable loss of barium values by forming water-insoluble barium compounds (14). For example, barium sulfate can form the orthosilicate... [Pg.477]

Because of its extreme insolubility, barium sulfate is not toxic the usual antidote for poisonous barium compounds is to convert them to barium sulfate by administering sodium or magnesium sulfate. In medicine, barium sulfate is widely used as an x-ray contrast medium (see Imaging TECHNOLOGY X-RAY technology). It is also used in photographic papers, filler for plastics, and in concrete as a radiation shield. Commercially, barium sulfate is sold both as natural barite ore and as a precipitated product. Blanc fixe is also used in making white sidewall rubber tires or in other mbber applications. [Pg.482]


See other pages where Sulfate insoluble barium is mentioned: [Pg.280]    [Pg.141]    [Pg.142]    [Pg.141]    [Pg.65]    [Pg.84]    [Pg.37]    [Pg.807]    [Pg.42]    [Pg.31]    [Pg.409]    [Pg.19]    [Pg.31]    [Pg.245]   
See also in sourсe #XX -- [ Pg.245 ]




SEARCH



Barium sulfate, insolubility

Sulfates barium sulfate

© 2024 chempedia.info