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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.
Hard water usually contains calcium or magnesium ions. Sodium carbonate is used for removing these ions and replacing them with sodium ions. [16] Sodium carbonate is a water-soluble source of carbonate. The calcium and magnesium ions form insoluble solid precipitates upon treatment with carbonate ions:
The tables below provides information on the variation of solubility of different substances (mostly inorganic compounds) in water with temperature, at one atmosphere pressure. Units of solubility are given in grams of substance per 100 millilitres of water (g/100 ml), unless shown otherwise. The substances are listed in alphabetical order.
Trona (trisodium hydrogendicarbonate dihydrate, also sodium sesquicarbonate dihydrate, Na 2 CO 3 ·NaHCO 3 ·2H 2 O) is a non-marine evaporite mineral. [4] [6] It is mined as the primary source of sodium carbonate in the United States, where it has replaced the Solvay process used in most of the rest of the world for sodium carbonate production.
Lithium, sodium, potassium, rubidium, caesium, and ammonium carbonates are water-soluble salts, but carbonates of 2+ and 3+ ions are often poorly soluble in water. Of the insoluble metal carbonates, CaCO 3 is important because, in the form of scale, it accumulates in and impedes flow through pipes.
The two reactions (2) and (4) describe the equilibrium between bicarbonate ions (HCO 3 −), which are highly soluble in water and calcium carbonate (CaCO 3) salt. According to Le Chatelier's principle , drilling operations and extraction of the oil from the well bore decreases the pressure of the formation and the equilibrium shifts to the ...
Without the presence of dissolved NaOH or KOH, responsible for the high pH (~13.5) of the concrete pore water, the amorphous silica of the reactive aggregates would not be dissolved and the reaction would not evolve. Moreover, the soluble sodium or potassium silicate is very hygroscopic and swells when it absorbs water.
The ammonia from reaction (III) is recycled back to the initial brine solution of reaction (I). The sodium bicarbonate (NaHCO 3) precipitate from reaction (I) is then converted to the final product, sodium carbonate (washing soda: Na 2 CO 3), by calcination (160–230 °C), producing water and carbon dioxide as byproducts: