Rare earth doped yttrium oxide fluorescent nano-fiber and preparation method thereof
A fluorescent nanofiber and rare earth doping technology, applied in the field of fluorescent nanofibers and their preparation, can solve the problems of large particle size, low strength and efficiency, small specific surface area, etc., and achieve easy recovery, easy operation, and large specific surface area. Effect
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example 1
[0030] 1. Preparation of electrospinning solution: 7.5g polyvinyl alcohol (polymerization degree 1788), 4.5g Y (NO 3 ) 3 / Eu(NO 3 ) 3 (atomic ratio Eu:(Y+Eu)=5%) and 67.5 mL of distilled water were mixed, and a homogeneous spinning solution was formed after stirring at 80° C. for a period of time.
[0031] 2. PVA / Y (NO) was prepared by electrospinning of the spinning solution through electrospinning equipment at a voltage of 65KV, the distance between the spinneret and the receiving device was 18cm, the feeding flow rate of the spinning solution was 1mL / 1h, and the electrospinning temperature was 50°C. 3 ) 3 / Eu(NO 3 ) 3 Composite nanofiber precursors.
[0032] 3. The prepared PVA / Y (NO 3 ) 3 / Eu(NO 3 ) 3 The composite nanofiber precursor was dried in a vacuum drying oven (vacuum degree of 0.03 MPa, temperature of 70 °C) for 8 h.
[0033] 4. Y(NO) after drying 3 ) 3 / Eu(NO 3 ) 3 The composite nanofiber precursors were calcined in a muffle furnace at 800 °C for 7...
example 2
[0035] 1. Preparation of electrospinning solution: 2.5g polyvinyl alcohol (polymerization degree 1788), 1.5g Y (NO 3 ) 3 / Er(NO 3 ) 3 (atomic ratio Er:(Y+Er)=10%) and 22.5 mL of distilled water were mixed, and a homogeneous spinning solution was formed after stirring at 80° C. for a period of time.
[0036] 2. PVA / Y (PVA / Y ( NO 3 ) 3 / Er(NO 3 ) 3 Composite nanofiber precursors.
[0037] 3. The prepared PVA / Y (NO 3 ) 3 / Er(NO 3 ) 3 The composite nanofiber precursor was dried in a vacuum drying oven (vacuum degree of 0.02 MPa, temperature of 70 °C) for 8 h.
[0038] 4. PVA / Y(NO) after drying 3 ) 3 / Er(NO 3 ) 3 The composite nanofiber precursors were calcined in a muffle furnace at 800 °C for 7 h. Preparation of Y with a diameter ranging from 200 to 500 nm 2 O 3 :Er fluorescent nanofibers. The weight percent content of yttrium oxide and erbium oxide: 84.2% of yttrium oxide and 15.8% of erbium oxide.
example 3
[0040] 1. Preparation of electrospinning solution: 7.5g polyvinyl alcohol (polymerization degree 1788), 4.5g Y (NO 3 ) 3 / Tb(NO 3 ) 3 (atomic ratio Tb:(Y+Tb)=1%) and 67.5 mL of distilled water were mixed and stirred at 80° C. for a period of time to form a uniform spinning solution.
[0041] 2. PVA / Y (PVA / Y ( NO 3 ) 3 / Tb(NO 3 ) 3 Composite nanofiber precursors.
[0042] 3. The prepared PVA / Y (NO 3 ) 3 / Tb(NO 3 ) 3 The composite nanofiber precursor was dried in a vacuum drying oven (vacuum degree of 0.03 MPa, temperature of 70 °C) for 8 h.
[0043] 4. PVA / Y(NO) after drying 3 ) 3 / Tb(NO 3 ) 3 The composite nanofiber precursors were calcined in a muffle furnace at 800 °C for 7 h. Preparation of Y with a diameter ranging from 100 to 250 nm 2 O 3 : Tb fluorescent nanofibers. The weight percent content of yttrium oxide and terbium oxide: 98.37% of yttrium oxide, 1.63% of terbium oxide.
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