Barium sulfate, insolubility

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... 

Barite, predominately BaSO, meets the overall requirements for weighting material better than other materials and is used for increasing the density of drilling fluids throughout the world. Commercial barite has a lower specific gravity than pure barium sulfate owing to the presence of associated minerals, such as silica. Barite is virtually insoluble in water and does not react with other mud constituents. Most operators prefer barite that meets API specifications (Table 2) (23). The barite content in mud depends on the desired density but can be as high as 2000 kg/km (700 lb/bbl). 

Most of the heavy-metal impurities present in 2inc salt solutions must be removed before the precipitation reaction, or these form insoluble colored sulfides that reduce the whiteness of the 2inc sulfide pigment. This end is usually achieved by the addition of 2inc metal which reduces most heavy-metal ions to their metallic form. The brightness of 2inc sulfide can be improved by the addition of a small amount of cobalt salts (ca 0.04% on a Co/Zn basis) (20). Barium sulfate [7727-43-7] formed in the first step is isolated and can be used as an extender. 

The fused product contains about 60—85% barium sulfide, unreacted barium sulfate, and impurities present in barite and ash. The soluble barium sulfide is extracted from the mixture with water and separated from the insoluble impurities by filtration. 

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. 

Thiosulfates are generally prepared by treating aqueous solutions of either calcium or barium thiosulfate with the corresponding carbonate or sulfate of the desired metal. The insoluble calcium or barium sulfates or carbonates are filtered and the thiosulfate recovered from the filtrate by vacuum evaporation. 

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. 

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). 

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). 

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. 

According to the flowchart, salts of chloride and sulfate are soluble. Therefore, no precipitate will form unless one of these compounds is included among the exceptions listed in Table 4A - Barium sulfate is one of these exceptions, so it is an insoluble salt. 

The solubility guidelines can be used to design ways of making salts. Suppose that we want to prepare barium sulfate, BaSOq. This substance is opaque to X rays, so it is often used to visualize the intestinal tract. Patients are given a barium cocktail, and then the areas of interest are irradiated. Barium sulfate absorbs the X rays to give a picture of the intestines. Soluble barium salts are poisonous, but BaSOq is insoluble in water, so it can be administered safely. (Only 1.0 X 10" mol dissolves in 1 L ofwaterat25 °C.)... 

C16-0027. Barium sulfate is a relatively insoluble salt used for medical radiographs of the gastrointestinal tract BaSOq (.S ) Ba " (a g) + SOq (a q) The concentration of Ba " ions in a... 

When a substance made up of ions is dissolved in water, the dissolved ions behave independently. That is, they undergo their own characteristic reactions regardless of what other ions may be present. For example, barium ions in solution, Ba2, always react with sulfate ions in solution, S04 , to form an insoluble ionic compound, BaS04(s), no matter what other ions are present in the barium solution. If a solution of barium chloride, BaCK, and a solution of sodium sulfate, Na S04, arc mixed, a white solid, barium sulfate, is produced. The solid can be separated from the solution by filtration, and the resulting solution contains sodium chloride, just as it would if solid NaCl were added to water. In other words, when the two solutions are mixed, the following reaction occurs ... 

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

The bomb method for sulfur determination (ASTM D129) uses sample combustion in oxygen and conversion of the sulfur to barium sulfate, which is determined by mass. This method is suitable for samples containing 0.1 to 5.0% w/w sulfur and can be used for most low-volatility petroleum products. Elements that produce residues insoluble in hydrochloric acid interfere with this method this includes aluminum, calcium, iron, lead, and silicon, plus minerals such as asbestos, mica, and silica, and an alternative method (ASTM D1552) is preferred. This method describes three procedures the sample is first pyrolyzed in either an induction furnace or a resistance furnace the sulfur is then converted to sulfur dioxide, and the sulfur dioxide is either titrated with potassium iodate-starch reagent or is analyzed by infrared spectroscopy. This method is generally suitable for samples containing from 0.06 to 8.0% w/w sulfur that distill at temperatures above 177°C (351°F). 

Compounds Soluble—barium nitrate, barium sulfide, barium chloride, barium hydroxide, barium acetate insoluble—barium sulfate... 

All barium salts, especially the water and acid-soluble compounds, are highly toxic. Barium ion can cause death through ventricular fibrillation of the heart. It is a stimulant to the heart muscle. Intake of a few grams of barium salt can be lethal to humans. The insoluble salts such as barium sulfate, however, have little toxic action. 

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. 

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. 

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... 

Barium sulfate is one of the most insoluble salts of barium. It does not undergo double decomposition reactions in aqueous phase. It dissolves in concentrated H2SO4 to form an acid sulfate which breaks down to BaS04 upon dilution. 

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. 

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 ... 

Before concentration, acid hydrolyzates are neutralized, most commonly with barium carbonate, although such organic bases as methyldioctylamine has been used.81 This step normally causes little loss, except by adsorption on, for example, barium sulfate,82 but the following points are of interest. Neutralization with ammonia has been recommended,83 as the neutral solution may be evaporated directly to dryness without filtration, and the ammonium sulfate formed is insoluble in methyl sulfoxide, a solvent used for trimethyl-silylation. The authors83 also found that, when hydrolyzates are neutralized with ion-exchange resins, the pH of the concentrated solutions may differ by as much as 2 units of pH. D-Fructose has been found to be epimerized by barium carbonate or pyridine, and lead... 

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. 

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... 

Both zinc sulfide and barium sulfate are insoluble in water. To improve the stability of lithopone, a small amount of a cobalt salt is added to the precipitated mixture. The mixture has to be filtered off, dried, and calcined. The calcination is carried out in rotary calciners at temperatures between 600 and 700°C. During calcination, the particle size of zinc sulfide grows from its original size (about 0.1 Jim) to the pigmentary optimal size of 0.4—0.6 Jim. 

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