Inorganic antiseptic of RE activated silver carrying matter and its prepn
An inorganic antibacterial agent and technology of antibacterial agent are applied in the field of rare earth activated silver-loaded inorganic antibacterial agent and its preparation field, which can solve the problems of easy discoloration and blackening, easy blackening of antibacterial agent, influence on popularization and use, etc., and achieves good heat resistance. , The effect of good discoloration resistance
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Embodiment 1
[0023] The prepared sodium zirconium hydroxyphosphate 50g was placed in a beaker, and dispersed under electric stirring for 2 hours; Zn(NO 3 ) 2 2.5g, AgNO 3 1.0 g, and respectively made into 10wt% solution with deionized water.
[0024] Adjust the temperature of the water bath at 60°C, place the beaker with the carrier sodium zirconium hydroxyphosphate in the water bath; add silver nitrate solution and zinc nitrate solution in sequence while continuing to stir; then add dilute nitric acid or NaOH solution to adjust its pH The value is 4. Weighed 0.5 g of the rare earth element compound lanthanum nitrate, made it into a 1 wt % solution, added it to the above emulsion, kept the temperature at 60° C., and carried out the ion exchange reaction for 4 hours. Then the emulsion was vacuum filtered, washed three times with deionized water, and the obtained filter cake was calcined at 800° C., and then ground and pulverized to obtain Sample 1.
Embodiment 2
[0026] The prepared sodium zirconium hydroxyphosphate 50g was placed in a beaker and dispersed under electric stirring for 2 hours; respectively weighed Cu(NO 3 ) 2 1.0g, Zu(NO 3 )3.0g, AgNO 3 2.0g, and were made into 10wt% solution with deionized water.
[0027] Adjust the temperature of the water bath at 70°C, place the beaker with the carrier sodium zirconium hydroxyphosphate in the water bath; add silver nitrate solution, copper nitrate solution, and zinc nitrate solution in sequence while continuing to stir; then add dilute nitric acid or NaOH solution , adjust its pH value to 3. Weigh 0.5 g of the rare earth element compound yttrium nitrate, prepare a 1 wt % solution, add it to the above emulsion, keep the temperature at 70° C., and carry out ion exchange reaction for 5 hours. Then the emulsion was vacuum filtered, washed three times with deionized water, and the obtained filter cake was calcined at 700° C., and then ground and pulverized to obtain sample 2.
Embodiment 3
[0029] The prepared sodium zirconium hydroxyphosphate 50g was placed in a beaker and dispersed under electric stirring for 2 hours; respectively weighed Cu(NO 3 ) 2 1.0g, Zu(NO 3 ) 2.0g, AgNO 3 2.0g, and were made into 10wt% solution with deionized water.
[0030] Adjust the temperature of the water bath at 60°C, place the beaker with the carrier sodium zirconium hydroxyphosphate in the water bath; add silver nitrate solution, zinc nitrate solution, and copper nitrate solution in sequence while continuing to stir; then add dilute nitric acid or NaOH solution , adjust its pH value to 4. Weighed 0.5 g of the rare earth element compound lanthanum nitrate, made it into a 1 wt % solution, added it to the above emulsion, kept the temperature at 60° C., and carried out the ion exchange reaction for 4 hours. Then the emulsion was vacuum filtered, washed three times with deionized water, and the obtained filter cake was calcined at a temperature of 800° C., and then ground and pulv...
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