Method for controlling mutual transformation between calcite and vaterite by using calcium source concentration
A technology of calcite and vaterite, applied in the field of biomimetic materials, achieves the effects of high repeatability, fast response speed, and low environmental conditions
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Embodiment 1
[0041] Step 1: inoculate S.pasteurii on the culture medium, and culture it in a shaking incubator at 30°C and 100r / min for 48 hours to obtain a bacterial liquid; wherein, the culture medium includes yeast extract 10~ 30g / L, ammonium sulfate 15g / L, the pH of the medium is 7-9.5;
[0042] Step 2: configure the mixed solution of urea and calcium acetate monohydrate as a nutrient salt solution, wherein the concentration of urea is 0.5mol / L, and the concentration of calcium acetate monohydrate is 0.025mol / L;
[0043] Step 3: Prepare 0.2g / L urease solution (urease activity is 137u / mg), add the urease solution into the nutrient salt solution, and the volume ratio of the nutrient salt solution to the urease solution is 9:1;
[0044] Step 4: Add the bacterial liquid to the mixed solution of urease and nutrient salt, the volume ratio of the bacterial liquid to the mixed solution is 1:10, shake evenly, and stand at 20°C for 72 hours;
[0045] Step 5: Ultrasonic treatment at 20-40°C for 30...
Embodiment 2
[0051] Step 1: inoculate S.pasteurii on the culture medium, and culture it in a shaking incubator at 30°C and 100r / min for 48 hours to obtain a bacterial liquid; wherein, the culture medium includes yeast extract 10~ 30g / L, ammonium sulfate 15g / L, the pH of the medium is 7-9.5;
[0052] Step 2: configure the mixed solution of urea and calcium acetate monohydrate as a nutrient salt solution, wherein the concentration of urea is 0.5mol / L, and the concentration of calcium acetate monohydrate is 0.1mol / L;
[0053] Step 3: Prepare 0.2g / L urease solution (urease activity is 137u / mg), add urease solution into nutrient salt solution, the volume ratio of nutrient salt solution to urease solution is 8:1;
[0054] Step 4: Add the bacterial liquid to the mixed solution of urease and nutrient salt, the volume ratio of the bacterial liquid to the mixed solution is 1:10, shake evenly, and stand at 20°C for 72 hours;
[0055] Step 5: Ultrasonic treatment at 20-40°C for 30min-1h to obtain a s...
Embodiment 3
[0061] Step 1: inoculate S.pasteurii on the culture medium, and culture it in a shaking incubator at 30°C and 100r / min for 48 hours to obtain a bacterial liquid; wherein, the culture medium includes yeast extract 10~ 30g / L, ammonium sulfate 15g / L, the pH of the medium is 7-9.5;
[0062] Step 2: configure the mixed solution of urea and calcium acetate monohydrate as a nutrient salt solution, wherein the concentration of urea is 0.5mol / L, and the concentration of calcium acetate monohydrate is 0.3mol / L;
[0063] Step 3: Prepare 0.2g / L urease solution (urease activity is 110u / mg), add urease solution into nutrient salt solution, the volume ratio of nutrient salt solution to urease solution is 9:1;
[0064] Step 4: Add the bacterial liquid to the mixed solution of urease and nutrient salt, the volume ratio of the bacterial liquid to the mixed solution is 1:10, shake evenly, and stand at 10°C for 72 hours;
[0065] Step 5: Ultrasonic treatment at 20-40°C for 30min-1h to obtain a s...
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