Up-conversion light diffusion micro-sphere for panel display and preparation method thereof
A flat-panel display and light conversion technology, which is applied in the preparation of microspheres and microcapsule preparations, can solve the problem of poor mechanical properties and flame retardancy of the light-diffusing film, the inability to realize the multi-functionality of the light-diffusing film, and the shape and size of the light-diffusing agent. Uncontrollable and other issues, to achieve strong up-conversion luminous performance, good application prospects, and multi-functional effects
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Examples
Embodiment 1
[0032] At 25°C, mix 0.14mol magnesium nitrate, 1.02g composite precipitant (the mass ratio of ammonium bicarbonate, cetyltrimethylammonium bromide, and sodium hydroxide is 1:2:0.5), 4mmol ErCl 3 ·H 2 0. Add 60mL distilled water into the reaction kettle and mix evenly, heat up to 150°C after ultrasonic dispersion for 1h, hydrothermally react for 8h, filter after cooling down to room temperature, wash with 100mL distilled water and 60mL absolute ethanol each time, wash 3 times, at 90 Dry at ℃ for 12h to get Er 2 o 3 - MgO microspheres.
[0033] After mixing 1.5g of melamine with 50mL of absolute ethanol, add 4g of the above-prepared Er 2 o 3 -MgO microspheres, stirred at 25°C for 8h, evaporated ethanol under reduced pressure, dried the solid at 60°C for 10h, and calcined at 550°C for 4h in an air atmosphere, the porous g-C 3 N 4 / Er 2 o 3 -MgO composite microspheres.
[0034] At 25°C, 0.01mol N-(β-aminoethyl)-γ-aminopropyltrimethoxysilane, 80mL distilled water, 10g urea...
Embodiment 2
[0037] At 25°C, mix 0.14mol magnesium nitrate, 1g composite precipitant (the mass ratio of ammonium bicarbonate, cetyltrimethylammonium bromide, and sodium hydroxide is 1:3:0.5), 3mmol Er(NO 3 ) 3 ·5H 2 0, 50mL distilled water, add to the reaction kettle and mix evenly, heat up to 160°C after ultrasonic dispersion for 0.5h, hydrothermally react for 6h, filter after cooling down to room temperature, wash with 100mL distilled water and 60mL absolute ethanol each time, wash 4 times, in Dry at 80°C for 24h to get Er 2 o 3 - MgO microspheres.
[0038] After mixing 3g of dicyandiamide with 80mL of absolute ethanol, add 5g of Er prepared above 2 o 3 -MgO microspheres, stirred at 25°C for 6h, evaporated the ethanol under reduced pressure, dried the obtained solid in vacuum at 70°C for 9h, and calcined at 600°C for 3h in an air atmosphere, the porous g-C 3 N 4 / Er 2 o 3 -MgO composite microspheres.
[0039] At 25°C, 0.012mol N-(β-aminoethyl)-γ-aminopropyltrimethoxysilane, 85m...
Embodiment 3
[0042] At 25°C, mix 0.14mol magnesium nitrate, 1.03g composite precipitant (the mass ratio of ammonium bicarbonate, cetyltrimethylammonium bromide, and sodium hydroxide is 1:3:1.5), 60mL distilled water, 4 mmol ErCl 3 ·H 2 O, add to the reaction kettle and mix well, heat up to 140°C after ultrasonic dispersion for 1.5h, hydrothermal reaction for 5h, filter after cooling down to room temperature, wash with 55mL distilled water and 40mL absolute ethanol each time, wash 3 times, at 100°C Dry for 10h to get Er 2 o 3 - MgO microspheres.
[0043] After mixing 3 g of melamine with 90 mL of absolute ethanol, add 6 g of Er prepared above 2 o 3 -MgO microspheres, stirred at 25°C for 10h, evaporated ethanol under reduced pressure, dried the solid at 50°C for 9h, and calcined at 450°C for 6h in an air atmosphere, the porous g-C 3 N 4 / Er 2 o 3 -MgO composite microspheres.
[0044] At 25°C, 0.01mol N-(β-aminoethyl)-γ-aminopropyltrimethoxysilane, 80mL distilled water, 10g urea, 3g...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com