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ca(oh) 2 + h 2 o 2 → cao 2 + 2 h 2 o The octahydrate precipitates upon the reaction of calcium hydroxide with dilute hydrogen peroxide . Upon heating it dehydrates.
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.
Calcium hydroxide is modestly soluble in water, as seen for many dihydroxides. Its solubility increases from 0.66 g/L at 100 °C to 1.89 g/L at 0 °C. [8] Its solubility product K sp of 5.02 × 10 −6 at 25 °C, [1] its dissociation in water is large enough that its solutions are basic according to the following dissolution reaction:
Carbonatation is a slow process that occurs in concrete where lime (CaO, or Ca(OH) 2 ) in the cement reacts with carbon dioxide (CO 2) from the air and forms calcium carbonate. The water in the pores of Portland cement concrete is normally alkaline with a pH in the range of 12.5 to 13.5.
Substance Formula 0 °C 10 °C 20 °C 30 °C 40 °C 50 °C 60 °C 70 °C 80 °C 90 °C 100 °C Barium acetate: Ba(C 2 H 3 O 2) 2: 58.8: 62: 72: 75: 78.5: 77: 75
The less soluble Mg(OH) 2 precipitates because of the common ion effect due to the OH − added by the dissolution of Ca(OH) 2: [7] Mg 2+ + Ca(OH) 2 → Mg(OH) 2 + Ca 2+ For seawater brines, precipitating agents other than Ca(OH) 2 can be utilized, each with their own nuances: Use of Ca(OH) 2 can yield CaSO 4 or CaCO 3, which reduces the final ...
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The alkali–carbonate reaction is an alteration process first suspected in the 1950s in Canada for the degradation of concrete containing dolomite aggregates. [1] [2]Alkali from the cement might react with the dolomite crystals present in the aggregate inducing the production of brucite, (MgOH) 2, and calcite (CaCO 3).