Method for preparing medical ultrafine barium sulfate
A technology of ultra-fine barium sulfate and preparation steps, which is applied in the field of preparation of medical ultra-fine barium sulfate, can solve problems such as uneven particle size distribution, low purity, and particle agglomeration, so as to simplify the production process, reduce production costs, and improve production efficiency. quality effect
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example 1
[0019] Weigh 5g of filter paper, cut it into 0.5cm pieces, then weigh 3g of sucrose, 0.5g of peptone, and 15g of agar in sequence, add them to a petri dish filled with 1L of deionized water, and use a concentration of 4mol / L sodium bicarbonate solution Adjust the pH to 7.2, then transfer the mixture to a pressure steam sterilizer, and sterilize it under the condition of 0.08MPa for 20 minutes to obtain a culture medium; inoculate the sporophage cellulobacteria into the above culture medium according to the inoculum size of 4%, and then Move the culture medium to a constant temperature incubator, cultivate it at 30°C for 6 days, rinse the surface of the culture medium with 100mL deionized water, collect the washing liquid, and obtain mycelium suspension; weigh 200g of non-woven fabric, cut it into pieces Add 0.6cm fragments into a reaction kettle filled with 200mL of deionized water, raise the temperature to 40°C, start the stirrer, set the speed at 300r / min, stir at a constant ...
example 2
[0023] Weigh 8g of filter paper, cut it into 1cm pieces, then weigh 4g of sucrose, 0.8g of peptone, and 20g of agar in turn, add them to a petri dish filled with 1.5L of deionized water, and use a concentration of 5mol / L sodium bicarbonate solution Adjust the pH to 7.3, then transfer the mixture to a pressure steam sterilizer, and sterilize it under the condition of 0.09MPa for 25 minutes to obtain a culture medium; inoculate the sporophage cellulobacteria into the above culture medium according to the inoculum size of 5%, and then Move the culture medium to a constant temperature incubator, cultivate it at 32°C for 7 days, rinse the surface of the culture medium with 150mL deionized water, collect the washing liquid, and obtain mycelium suspension; weigh 250g of non-woven fabric, cut it into pieces Add 0.7cm fragments into a reaction kettle filled with 250mL of deionized water, raise the temperature to 42°C, start the stirrer, set the speed at 400r / min, stir at a constant temp...
example 3
[0027] Weigh 10g of filter paper, cut it into 1.5cm pieces, then weigh 5g of sucrose, 1.0g of peptone, and 25g of agar in sequence, add them to a petri dish filled with 2L of deionized water, and use a concentration of 6mol / L sodium bicarbonate solution Adjust the pH to 7.5, then transfer the mixture to a pressure steam sterilizer, and sterilize it under the condition of 0.1 MPa for 30 minutes to obtain a culture medium; inoculate the sporophage cellulobacteria into the above culture medium according to the inoculum size of 6%, and then Move the culture medium to a constant temperature incubator, cultivate it at 35°C for 8 days, rinse the surface of the culture medium with 200mL deionized water, collect the washing liquid, and obtain mycelial suspension; weigh 300g of non-woven fabric, cut it into pieces Add 0.8cm fragments into a reaction kettle filled with 300mL of deionized water, raise the temperature to 45°C, start the stirrer, set the speed at 500r / min, stir at a constant...
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