Eureka AIR delivers breakthrough ideas for toughest innovation challenges, trusted by R&D personnel around the world.

Method for synthesizing one-dimensional red long afterglow material

A long afterglow material and long afterglow luminescence technology, applied in the direction of luminescent materials, chemical instruments and methods, etc.

Inactive Publication Date: 2015-02-11
TAIYUAN UNIV OF TECH
View PDF7 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, the amount of CS2 generated by this method is very small, resulting in a very small amount of yttrium hydroxide that can be vulcanized, and the prepared Y2O2 sub>S: Eu3+, Mg2+, Ti4+ Red long afterglow luminescent material only partially luminescent

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Method for synthesizing one-dimensional red long afterglow material
  • Method for synthesizing one-dimensional red long afterglow material
  • Method for synthesizing one-dimensional red long afterglow material

Examples

Experimental program
Comparison scheme
Effect test

Embodiment approach 1

[0045] The raw material yttrium oxide, europium nitrate, magnesium nitrate, butyl titanate, nitric acid, and sodium hydroxide are configured into solutions of corresponding concentrations, and Y(NO 3 ) 3 Solution 20ml, the concentration is 0.05mol / L Eu(NO 3 ) 3 Solution 6ml, the concentration is 0.05mol / L Mg(NO 3 ) 2 Solution 2ml, the concentration is 0.05mol / L of C 16 h 36 o 4 Ti solution 2ml. After mixing the above solutions, add 42 ml of a mixture of absolute ethanol and deionized water (V 去离子水 :V 无水乙醇 =2:1). After fully stirring evenly, add 4mol / L NaOH solution to the solution to adjust the pH value to 13. Put it into a high-pressure reactor, place it in a drying oven, and heat up to 180 o C, constant temperature for 12h. Cool to room temperature, wash with deionized water repeatedly 3~4 times, oC The precursor is obtained by drying. The prepared medicine is put into a small alumina crucible, and then covered with a large crucible, and the interlayer is filled...

Embodiment approach 2

[0047] The raw material yttrium oxide, europium nitrate, magnesium nitrate, butyl titanate, nitric acid, and sodium hydroxide are configured into solutions of corresponding concentrations, and Y(NO 3 ) 3 Solution 20ml, the concentration is 0.05mol / L Eu(NO 3 ) 3 Solution 6ml, the concentration is 0.05mol / L Mg(NO 3 ) 2 Solution 2ml, the concentration is 0.05mol / L of C 16 h 36 o 4 Ti solution 2ml. After mixing the above solutions, add 42 ml of a mixture of absolute ethanol and deionized water (V 去离子水 :V 无水乙醇 =2:1), after fully stirring evenly, add 4mol / L NaOH solution to the solution, adjust the pH value to 13, put it in a high-pressure reaction kettle, put it in a drying box, and raise the temperature to 180 o C, keep the temperature for 12h, cool to room temperature, wash with deionized water repeatedly for 3~4 times, at 60 oC The precursor is obtained by drying. The prepared precursor is put into a small alumina crucible, and then covered with a large crucible, and...

Embodiment approach 3

[0049] The raw material yttrium oxide, europium nitrate, magnesium nitrate, butyl titanate, nitric acid, and sodium hydroxide are configured into solutions of corresponding concentrations, and Y(NO 3 ) 3 Solution 20ml, the concentration is 0.05mol / L Eu(NO 3 ) 3 Solution 6ml, the concentration is 0.05mol / L Mg(NO 3 ) 2 Solution 2ml, the concentration is 0.05mol / L of C 16 h 36 o 4 Ti solution 2ml. After mixing the above solutions, add 42 ml of a mixture of absolute ethanol and deionized water (V 去离子水 :V 无水乙醇 =2:1). After fully stirring evenly, add 4mol / L NaOH solution to the solution to adjust the pH value to 13. Put it into a high-pressure reactor, place it in a drying oven, and heat up to 180 o C, constant temperature for 12h. Cool to room temperature, wash with deionized water repeatedly 3~4 times, oC The precursor is obtained by drying. The prepared medicine is put into a small alumina crucible, and then covered with a large crucible, and the interlayer is filled...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
diameteraaaaaaaaaa
lengthaaaaaaaaaa
diameteraaaaaaaaaa
Login to View More

Abstract

The invention discloses a method for synthesizing a one-dimensional red long afterglow material, and belongs to the technical field of preparation of a phosphor material. The method is characterized by comprising the steps of carrying out hydrothermal reaction on Y3<+>, Eu<3+>, Mg<2+>, and Ti<4+> at the same time to generate a Y(OH)3 precursor doped with Eu<3+>, Mg<2+>, and Ti<4+>, vulcanizing the precursor by mixture of carbon powder and sublimed sulfur to generate a one-dimensional Y2O2S:Eu<3+>, Mg<2+>, and Ti<4+> red long afterglow luminescent material. The red long afterglow luminescent material prepared by the method disclosed by the invention is low in crystallization temperature of the substrate; ions which need to be doped are doped into the substrate at the hydrothermal stage of fabricating the precursor; the good nano tubular structure of a sample can be kept in later vulcanizing and sintering processes; and the physical and chemical properties are stable.

Description

technical field [0001] The invention discloses a method for synthesizing a one-dimensional red long-lasting luminescent material, which belongs to the technical field of phosphorescent material preparation, and specifically relates to a method for combining Y 3+ 、Eu 3+ , Mg 2+ and Ti 4+ At the same time, the hydrothermal reaction produces Eu 3+ , Mg 2+ and Ti 4+ Doped Y(OH) 3 precursor, followed by sulfuration of Y(OH) with a mixture of carbon powder and sublimated sulfur 3 Prebody generation 1D Y 2 o 2 S: Eu 3+ , Mg 2+ , Ti 4+ Red long-lasting glow material approach. Background technique [0002] Rare-earth long-lasting luminescent materials can store energy under sunlight, and then slowly release energy in a dark background to emit light. This feature is widely used in low-light lighting, emergency instructions, architectural decoration and other fields. In recent years, Later, it gradually expanded to high-tech fields such as optical information storage...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Patents(China)
IPC IPC(8): C09K11/84
Inventor 崔彩娥王磊黄平姜国伟武银兰郝虎在
Owner TAIYUAN UNIV OF TECH
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Eureka Blog
Learn More
PatSnap group products