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Barium carbonate is the inorganic compound with the formula BaCO 3. Like most alkaline earth metal carbonates, it is a white salt that is poorly soluble in water. It occurs as the mineral known as witherite. In a commercial sense, it is one of the most important barium compounds. [5]
Its aqueous solution, if clear, is guaranteed to be free of carbonate, unlike those of sodium hydroxide and potassium hydroxide, as barium carbonate is insoluble in water. This allows the use of indicators such as phenolphthalein or thymolphthalein (with alkaline colour changes) without the risk of titration errors due to the presence of ...
Other compounds of barium find only niche applications, limited by the toxicity of Ba 2+ ions (barium carbonate is a rat poison), which is not a problem for the insoluble BaSO 4. Barium oxide coating on the electrodes of fluorescent lamps facilitates the release of electrons .
From water solutions of barium chloride, its dihydrate (BaCl 2 ·2H 2 O) can be crystallized as colorless crystals. [2] Barium chloride can in principle be prepared by the reaction between barium hydroxide or barium carbonate with hydrogen chloride. These basic salts react with hydrochloric acid to give hydrated barium chloride.
Barium acetate is generally produced by the reaction of acetic acid with barium carbonate: [2] BaCO 3 + 2 CH 3 COOH → (CH 3 COO) 2 Ba + CO 2 + H 2 O. The reaction is performed in solution and the barium acetate crystalizes out at temperatures above 41 °C. Between 25 and 40 °C, the monohydrate version crystalizes. Alternatively, barium ...
The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.
Barium nitrate is manufactured by two processes that start with the main source material for barium, the carbonate. The first involves dissolving barium carbonate in nitric acid, allowing any iron impurities to precipitate, then filtered, evaporated, and crystallized. The second requires combining barium sulfide with nitric acid. [4]
Barium carbonate is often added to maintain anhydrous and acid-free conditions. In the above reaction, while a mixture of isomeric allylic bromide products are possible, only one is created due to the greater stability of the 4-position radical over the methyl-centered radical.