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Microbiologically induced calcium carbonate precipitation (MICP) is a bio-geochemical process that induces calcium carbonate precipitation within the soil matrix. [1] Biomineralization in the form of calcium carbonate precipitation can be traced back to the Precambrian period. [ 2 ]
At extremely low P CO 2, dissolved CO 2, bicarbonate ion, and carbonate ion largely evaporate from the solution, leaving a highly alkaline solution of calcium hydroxide, which is more soluble than CaCO 3. For P CO 2 = 10 −12 atm, the [Ca 2+][OH −] 2 product is still below the solubility product of Ca(OH) 2 (8 × 10 −6).
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.
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
At the carbonate compensation depth, the rate of dissolution exactly matches the rate of supply of CaCO 3 from above. At steady state this depth, the CCD, is similar to the snowline (the first depth where carbonate-poor sediments occur). The lysocline is the depth interval between the saturation and carbonate compensation depths. [4] [1]
The calcium cycle is a transfer of calcium between dissolved and solid phases. There is a continuous supply of calcium ions into waterways from rocks, organisms, and soils. [1] [2] Calcium ions are consumed and removed from aqueous environments as they react to form insoluble structures such as calcium carbonate and calcium silicate, [1] [3] which can deposit to form sediments or the ...
Calcium carbonate saturation can be determined using the following equation: Ω = ([Ca 2+][CO 3 2−])/K sp. where the numerator ([Ca 2+][CO 3 2−]) denotes the concentration of calcium and carbonate ions and the denominator (K sp) refers to the mineral (solid) phase stoichiometric solubility product of calcium carbonate. [8]
Vaterite, like aragonite, is a metastable phase of calcium carbonate at ambient conditions at the surface of the Earth. As it is less stable than either calcite, the most stable polymorph, [ 5 ] or aragonite, vaterite has a higher solubility than either of these phases.