CN1185490A - Method for making artificial fluorescent precious stone - Google Patents

Method for making artificial fluorescent precious stone Download PDF

Info

Publication number
CN1185490A
CN1185490A CN 96122295 CN96122295A CN1185490A CN 1185490 A CN1185490 A CN 1185490A CN 96122295 CN96122295 CN 96122295 CN 96122295 A CN96122295 A CN 96122295A CN 1185490 A CN1185490 A CN 1185490A
Authority
CN
China
Prior art keywords
power
base material
substrate material
precious stone
add
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN 96122295
Other languages
Chinese (zh)
Inventor
郑岩
孙焕英
谢玉钧
杜春杰
郑玉宏
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
CHANGCHUN PHYS INST CHINESE
Original Assignee
CHANGCHUN PHYS INST CHINESE
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by CHANGCHUN PHYS INST CHINESE filed Critical CHANGCHUN PHYS INST CHINESE
Priority to CN 96122295 priority Critical patent/CN1185490A/en
Publication of CN1185490A publication Critical patent/CN1185490A/en
Pending legal-status Critical Current

Links

Abstract

A method for making an artificial fluorescent precious stone, uses ZnS as base material, Au and Cu as activation agent which accounts for 1 X (10 to the power -6) - 5 X (10 to the power -6) (in wt.) of said base material, and adds Cu which accounts for (in wt.) 5 X (10 to the power -6) - 5 X (10 to the power -5) of said base material, said added materials can be AuCl3, CuCl2 and CuSO4 etc., common activation agent can be DyCl3, accounting for (in wt.) 1 X (10 to the power -6) - 1 X (10 to the power -5) of the base material, and CsCl as fluxing agent accounting for (in wt.) 0.5-1% of the base material. Said materials are passed through wet grinding by adding distilled water, baking, growing for 5-12 hours by gas-phase transport method at 1050-1200 degree C, HCl gas flow. The obtained precious stone is in hexagonal structure, transparent bright green, 5 hours in after glow and has no radioactivity.

Description

The making method of artificial fluorescent precious stone
The invention belongs to the artificial crystal growth technology.
Hard mass is subjected to people with low basis, high quality and abundant colors to be liked, but the hard mass of fluorescent effect is not arranged at present as yet.
The making method that the purpose of this invention is to provide a kind of artificial fluorescent precious stone, this method technology is simple, the transparent bright green of the jewel of producing, it is also "dead" to reach 5 hours time of persistence.
For achieving the above object, the present invention adopts following technology:
Substrate material adopts ZnS, activator Au, Cu, and the add-on of Au is 1 * 10 of a substrate material weight -6-5 * 10 -6, the add-on of Cu is 5 * 10 of a substrate material weight -5* 10 -5, the adding form can be AuCl 3, CuCl 2, CuSO 4Deng, coactivator Dy, add-on is 1 * 10 of a substrate material weight -6-1 * 10 -5, its effect can improve after-glow brightness, and the adding form can be DyCl 3, fusing assistant CsCl, add-on is the 0.5-1% of substrate material weight, can improve crystalline quality, prolongs time of persistence.Above-mentioned materials adds the distilled water wet grinding, oven dry, and 1050-1200 ℃ of following gas phase axle fortune method grown the HCl air-flow 5-12 hour.The jewel of making belongs to hexagonal structure, emmission spectrum 480-520nm, mohs hardness 4.5-5, refractive index 2.3-2.4, chromatic dispersion 0.157.
Below in conjunction with embodiment the present invention is specified.
Embodiment 1. takes by weighing substrate material ZnS 100g, activator CuSO 4Middle Cu concentration 8 * 10 -6, AuCl 3Middle Au concentration 3 * 10 -6, coactivator DyCl 3The concentration 1 * 10 of middle Dy -6, fusing assistant CsCl 0.5g, adding distil water ground 48 hours, and silica tube is put in 120 ℃ of oven dry, 1100 ℃ of tube furnace temperature, HCl air-flow per minute 0.1L grew 8 hours.
Embodiment 2. takes by weighing substrate material ZnS 100g, activator CuSO 4Middle Cu concentration 5 * 10 -6, AuCl 3Middle Au concentration 5 * 10 -6, coactivator DyCl 3The concentration 2 * 10 of middle Dy -6, fusing assistant CsCl 1g, all the other conditions are with embodiment 1.
Embodiment 3. takes by weighing substrate material ZnS 100g, activator CuSO 4Middle Cu concentration 1 * 10 -5, AuCl 3Middle Au concentration 2 * 10 -6, coactivator DyCl 3The concentration 1 * 10 of middle Dy -5, fusing assistant CsCl 0.8g, all the other conditions are with embodiment 1.

Claims (1)

1, a kind of making method of artificial fluorescent precious stone is characterized in that substrate material adopts ZnS, activator Au, Cu, and the add-on of Au is 1 * 10 of a substrate material weight -5* 10 -6, the add-on of Cu is 5 * 10 of a substrate material weight -6-5 * 10 -5, the adding form can be AuCl 3, CuCl 2, CuSO 4Deng, coactivator Dy, add-on is 1 * 10 of a substrate material weight -6-1 * 10 -5, the adding form can be DyCl 3, fusing assistant CsCl, add-on is the 0.5-1% of substrate material weight, wet grinding, oven dry, 1050-1200 ℃ of following gas phase transport method grown the HCl air-flow 5-12 hour.
CN 96122295 1996-12-17 1996-12-17 Method for making artificial fluorescent precious stone Pending CN1185490A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 96122295 CN1185490A (en) 1996-12-17 1996-12-17 Method for making artificial fluorescent precious stone

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 96122295 CN1185490A (en) 1996-12-17 1996-12-17 Method for making artificial fluorescent precious stone

Publications (1)

Publication Number Publication Date
CN1185490A true CN1185490A (en) 1998-06-24

Family

ID=5127238

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 96122295 Pending CN1185490A (en) 1996-12-17 1996-12-17 Method for making artificial fluorescent precious stone

Country Status (1)

Country Link
CN (1) CN1185490A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1330736C (en) * 2002-09-30 2007-08-08 株式会社东芝 Phosphor for display device, its production method, and color display device using the same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1330736C (en) * 2002-09-30 2007-08-08 株式会社东芝 Phosphor for display device, its production method, and color display device using the same

Similar Documents

Publication Publication Date Title
Ben-Amotz et al. On the factors which determine massive β-carotene accumulation in the halotolerant alga Dunaliella bardawil
Kasperbauer Spectral distribution of light in a tobacco canopy and effects of end-of-day light quality on growth and development
Lichtenthaler et al. The importance of blue light for the development of sun-type chloroplasts
KR100477347B1 (en) Silicate phosphor with a long afterglow and manufacturing method thereof
Withrow et al. Photoperiodic responses of certain greenhouse annuals as influenced by intensity and wavelength of artificial light used to lengthen the daylight period
CN115466620B (en) Sodium europium gallium germanium garnet-based high-efficiency deep red fluorescent powder and preparation method thereof
US2660566A (en) Electroluminescent zinc sulfide phosphor
CN101402862B (en) Producing process for zinc sulfide long-afterglow luminescent powder
CN1185490A (en) Method for making artificial fluorescent precious stone
CN107439242A (en) A kind of control method for shortening plant growing cycle
CN1067097C (en) Preparation of rare earth Al203-B203 green luminescent material
US4316816A (en) Method for preparing copper-aluminum-gold-activated zinc-sulfide phosphors
CN113224222A (en) Preparation method of LED plant lamp light-emitting chip
CN1102170C (en) Combustion process for preparing long-afterglow phosphorescent powder
CN1186103A (en) Green fluorescent powder and preparation thereof
JPH02228389A (en) Self-activating zinc oxide phosphor
CN111849465A (en) Method for preparing high-performance quantum dot powder
Popovic et al. Oxygen‐quenched chlorophyll a fluorescence and electron transport in barley during greening
CN108998017A (en) One kind near-infrared long after glow luminous material of matrix containing silicon spinel and preparation method thereof
US4719387A (en) Infra-red phosphors and fluorescent lamp containing the same
SU1502497A1 (en) Luminescent glass
CN114686228B (en) Red light fluorescent powder and preparation method and application thereof
CN107306681B (en) A kind of control device shortening plant growing cycle
Morais et al. Growth and secondary product formation of in vitro cultures from the liverwort Reboulia hemisphaerica
Randall Luminescence and its Applications

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C01 Deemed withdrawal of patent application (patent law 1993)
WD01 Invention patent application deemed withdrawn after publication