Preparation method of antibacterial and antiviral nano water-based slurry
A water-based slurry, anti-virus technology, applied in the fields of botanical equipment and methods, nanotechnology, nanotechnology, etc.
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Embodiment 1
[0020] A method for preparing an antibacterial and antiviral nanocomposite powder aqueous slurry, characterized in that it comprises the following sequential steps:
[0021] (1) Take 0.1mol / L ZnSO 4 aqueous solution and 0.3mol / L NaOH aqueous solution with 50ml each, under the condition of magnetic stirring at 60°C, ZnSO 4 The solution was added dropwise to the NaOH solution. After the dropwise addition, the pH value of the solution was 11, and the water bath was kept warm for 2 hours; after the reaction was completed, the solid was separated by filtration and dried at 60°C to obtain a columnar nano ZnO powder. The average diameter of the prepared ZnO nanoparticles is 20nm-100nm;
[0022] (2) With 1%wt titanate coupling agent YY-2, 0.5%wt coconut oil monoethanolamide sulfosuccinic monoester disodium surfactant, 0.3%wt polyethylene glycol dispersant , mixed with 50%wt polyacrylic acid to form a mixed dispersion;
[0023] (3) Add GO aqueous solution and columnar nano-ZnO to Cu...
Embodiment 2
[0033] (1) Configure blank liquid medium: 0.5g of peptone, 0.25g of yeast extract, 0.25g of sodium chloride in 50ml of water and mix well), sterilize it at 121°C for a certain period of time, and cool to 60°C Afterwards, 20ul of Escherichia coli was added to the liquid medium and cultivated for 24h.
[0034] (2) Prepare sample medium: Add 2mg of nanocomposite powder aqueous slurry to 50ml of medium to prepare sample medium, sterilize at high temperature, and after cooling, take (1) 20ul of medium and transfer it to the next day’s sample culture medium for 24 hours.
[0035] (3) The prepared sample culture medium, physiological saline, petri dish, pipette tip, and LEP small tube are subjected to high-temperature sterilization together. After reaching 70°C, the sample culture medium was taken out and poured into a petri dish.
[0036] (4) Dilute the cultured sample culture medium and blank culture medium in a gradient manner, take 900ul of normal saline in 6 LEP small tubes, use...
Embodiment 3
[0042] Weigh 2 g of the nanocomposite powder water-based slurry in Example 1 into a sterile bottle, add 0.2 ml of parainfluenza virus liquid (1:1280) and mix at room temperature for 1 hour, shake for 4 minutes every 20 minutes, operate 3 times in total, add 4ml Bacterial saline, and immediately mix and shake for 4min. Aspirate the virus liquid for hemagglutination test, the measured virus hemagglutination titer is 1:30, and the virus adsorption and inactivation rate of the material is 100%.
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