Synthetic method of amorphous calcium carbonate
An amorphous calcium carbonate and synthesis method technology, applied in the direction of calcium carbonate/strontium/barium, etc., can solve the problems of poor controllability, and achieve the effect of cheap raw materials, easy access to raw materials, and simple operation
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Embodiment 1
[0030] 0.111 g CaCl 2 Dissolve in 100 ml of deionized water to form solution A, and dissolve 0.018 g of cetyltrimethylammonium bromide in solution A; dissolve 0.424 g of NaCO 3 Dissolve in 100 ml of deionized water to form solution B, and adjust the pH to 11 by adding 0.1 mol / L sodium hydroxide solution; put the two solutions of A and B in the refrigerator at 4°C for 40 minutes, and quickly remove the solution after taking it out B was added to solution A, stirred for 1 minute, and then centrifuged at a speed of 3000 rpm. The separated solid was washed twice with absolute ethanol, and finally dried in cold air at room temperature to obtain the product. X-ray diffraction The obtained product was characterized by XRD, which contained amorphous calcium carbonate and partially crystalline calcium carbonate.
Embodiment 2
[0032] 5.549 g CaCl 2 Dissolve in 100 ml of deionized water to form solution A, and dissolve 0.182 g of cetyltrimethylammonium bromide in solution A; dissolve 1.325 g of NaCO 3 Dissolve in 100 ml of deionized water to form solution B, and adjust the pH to 13 by adding 0.1 mol / L sodium hydroxide solution; put the two solutions of A and B in the refrigerator at 4°C for 60 minutes, and quickly remove the solution after taking it out B was added to solution A, stirred for 1 minute, and then centrifuged at a speed of 5000 rpm. The separated solid was washed twice with absolute ethanol, and finally dried in cold air at room temperature. The XRD pattern of the product was similar to that of Example 1.
Embodiment 3
[0034] 1.110 g CaCl 2 Dissolve in 100 ml of deionized water to form solution A, and dissolve 0.109 g of cetyltrimethylammonium bromide in solution A; dissolve 1.060 g of NaCO 3 Dissolve in 100 ml of deionized water to form solution B, and adjust the pH to 12 by adding 0.1 mol / L sodium hydroxide solution; put the two solutions of A and B in the refrigerator at 4°C for 50 minutes, and quickly remove the solution after taking it out B was added to solution A, stirred for 1 minute, and then centrifuged at a speed of 4000 rpm. The separated solid was washed twice with absolute ethanol, and finally dried in cold air at room temperature. The XRD pattern of the product was similar to that of Example 1.
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