A kind of preparation method of intercalation type metal oxide antibacterial agent
A technology of oxides and antibacterial agents, applied in the field of preparation of intercalated metal oxide antibacterial agents, can solve the problems of poor biological safety, high sterilization dosage, low toxic and side effects, etc., and achieves long durability, broad-spectrum sterilization, Low usage effect
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[0022] A kind of preparation method of intercalation type metal oxide antibacterial agent of the present invention comprises the following steps:
[0023] (1) Two-dimensional metal oxide synthesis: add 1mol / L~3mol / L manganese salt, tungsten salt or molybdenum salt solution into the autoclave, add reducing agent solution (reducing agent is glutathione, cysteine acid, cysteine hydrochloride, hydrogen peroxide, the concentration of the reducing agent solution is 3mol / L~6mol / L), mix well, adjust the pH value to 4-8 with acetic acid or ammonia water, and then Hydrothermal reaction at 120°C-250°C for 6-18 hours, centrifugal separation, drying at 25°C-100°C to obtain a two-dimensional metal oxide. Wherein, the volume ratio of the manganese salt, tungsten salt or molybdenum salt solution to the reducing agent solution is 1:1.
[0024] (2) Preparation of antibacterial agent: disperse the two-dimensional metal oxide in the mixed solution of water and organic solvent, then add 0.1mmol...
Embodiment 1
[0029] (1) Mix 100mL of 1mol / L ammonium molybdate solution and 100mL of 3mol / L glutathione aqueous solution, use acetic acid to adjust pH=4, react in water at 120°C for 18h, centrifugally wash, and dry at 25°C to obtain MoO x .
[0030] (2) MoO in step (1) x Disperse in water to form a 50mL 10mg / mL dispersion, add 1mL 0.1mmol / L copper nitrate solution and 1mL 0.1mg / mL ELB solution, peel off mechanically at 0-10°C for 0.5h, remove the sample and dry it at 80°C, Preparation of Cu@ELB@MoO x It is an intercalated metal oxide antibacterial agent.
Embodiment 2
[0032] (1) Mix 100mL 3mol / L ammonium molybdate aqueous solution and 100mL 6mol / L cysteine aqueous solution, adjust the pH to 4 with acetic acid, react in water at 250°C for 6h, centrifugally wash, and dry at 100°C to obtain MoO x .
[0033] (2) MoO in step (1) x Disperse in water to form a 50mL 10mg / mL dispersion, add 1mL 1mmol / L zinc nitrate solution and 1mL 10mg / mL ELB solution, peel off mechanically at 0-10°C for 5h, remove the sample and dry it at 80°C to obtain Zn @ELB @MoO x .
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