Preparation method and use of yttrium-doped bismuth stannate nanocrystallines
A technology of bismuth stannate and nanocrystals is applied in the field of inorganic nano-semiconductor material synthesis, which can solve the problem of high cost and achieve the effects of low cost, convenient mass production and reduced energy consumption.
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Embodiment 1
[0032] Take by weighing 1.94028g bismuth nitrate (Bi(NO 3 ) 3 ?5H 2 O) was dissolved in 10mL 1M dilute nitric acid to obtain mixed solution A; 1.13896g sodium stannate (Na 2 SnO 6 ?4H 2 O) Dissolve in 10ml double-distilled water to obtain an aqueous solution of sodium stannate, transfer the aqueous solution of sodium stannate into mixed solution A to obtain mixed solution B, adjust to pH=12 with NaOH solution. Transfer the mixed solution B with pH=12 into a 50mL polytetrafluoroethylene-lined reactor, and keep the temperature at 180°C for 24h. The product was alternately centrifuged and washed with water and ethanol, and dried in vacuum at 60° C. for 12 hours to obtain bismuth stannate nanocrystals.
[0033] Get 0.05g of the bismuth stannate nanocrystals prepared in this example and add them into a 100mL photocatalytic reactor containing 10mg / L tetracycline aqueous solution, and stir in the dark at room temperature for 30 minutes to reach adsorption-desorption equilibrium;...
Embodiment 2
[0035] Take by weighing 1.92087g bismuth nitrate (Bi(NO 3 ) 3 ?5H 2 O) and 0.00766g yttrium nitrate (Y(NO 3 ) 3 ·6H 2 O) was dissolved in 10mL 1M dilute nitric acid to obtain mixed solution A; 1.12757g sodium stannate (Na 2 SnO 6 ?4H 2O) Dissolve in 10ml double distilled water to obtain an aqueous solution of sodium stannate, transfer the aqueous solution of sodium stannate into the above mixed solution A to obtain a mixed solution B, and ultrasonically stir the mixed solution B until it becomes a milky white mixed solution , adjusted to pH=12 with NaOH solution. Transfer the mixed solution with pH=12 into a 50mL polytetrafluoroethylene-lined reactor, and keep the temperature at 180°C for 24h. The product was alternately centrifuged and washed with water and ethanol, and dried in vacuum at 60° C. for 12 hours to obtain yttrium-doped bismuth stannate nanocrystals.
[0036] The yttrium-doped bismuth stannate nanocrystals prepared in this example were used for photocatal...
Embodiment 3
[0038] Take by weighing 1.88207g bismuth nitrate (Bi(NO 3 ) 3 ?5H 2 O) and 0.02298g yttrium nitrate (Y(NO 3 ) 3 ·6H 2 O) was dissolved in 10mL 1M dilute nitric acid to obtain mixed solution A; 1.10479g sodium stannate (Na 2 SnO 6 ?4H 2 O) be dissolved in 10ml double-distilled water to obtain an aqueous solution of sodium stannate, transfer the aqueous solution of sodium stannate to mixed solution A to obtain mixed solution B, and ultrasonically stir mixed solution B until it becomes a milky white mixed solution, Adjust to pH=12 with NaOH solution. Transfer the mixed solution with pH=12 into a 50mL polytetrafluoroethylene-lined reactor, and keep the temperature at 180°C for 24h. The product was alternately centrifuged and washed with water and ethanol, and dried in vacuum at 60° C. for 12 hours to obtain yttrium-doped bismuth stannate nanocrystals.
[0039] The yttrium-doped bismuth stannate nanocrystals prepared in this example were used for photocatalytic degradation...
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