EP1412098A2 - Encapsulated long life electroluminescent phosphor - Google Patents
Encapsulated long life electroluminescent phosphorInfo
- Publication number
- EP1412098A2 EP1412098A2 EP00978609A EP00978609A EP1412098A2 EP 1412098 A2 EP1412098 A2 EP 1412098A2 EP 00978609 A EP00978609 A EP 00978609A EP 00978609 A EP00978609 A EP 00978609A EP 1412098 A2 EP1412098 A2 EP 1412098A2
- Authority
- EP
- European Patent Office
- Prior art keywords
- phosphor
- emission spectra
- coating
- electroluminescent
- electroluminescent phosphor
- 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.)
- Withdrawn
Links
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 title claims abstract description 53
- 238000000034 method Methods 0.000 claims abstract description 27
- 238000000295 emission spectrum Methods 0.000 claims abstract description 26
- 230000008569 process Effects 0.000 claims abstract description 23
- 239000011248 coating agent Substances 0.000 claims abstract description 22
- 238000000576 coating method Methods 0.000 claims abstract description 21
- 239000000203 mixture Substances 0.000 claims abstract description 8
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 claims abstract description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000001301 oxygen Substances 0.000 claims abstract description 7
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 7
- 238000004519 manufacturing process Methods 0.000 claims abstract description 5
- 239000002243 precursor Substances 0.000 claims abstract description 5
- 230000002939 deleterious effect Effects 0.000 claims abstract description 4
- 230000008859 change Effects 0.000 claims abstract description 3
- 239000010949 copper Substances 0.000 claims description 11
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 7
- 229910052802 copper Inorganic materials 0.000 claims description 7
- JLTRXTDYQLMHGR-UHFFFAOYSA-N trimethylaluminium Chemical group C[Al](C)C JLTRXTDYQLMHGR-UHFFFAOYSA-N 0.000 claims description 3
- 229910052984 zinc sulfide Inorganic materials 0.000 description 6
- 229910052782 aluminium Inorganic materials 0.000 description 5
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 239000005083 Zinc sulfide Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- 229910001868 water Inorganic materials 0.000 description 3
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 3
- OGIIWTRTOXDWEH-UHFFFAOYSA-N [O].[O-][O+]=O Chemical compound [O].[O-][O+]=O OGIIWTRTOXDWEH-UHFFFAOYSA-N 0.000 description 2
- 239000012190 activator Substances 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 230000004907 flux Effects 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- FFBHFFJDDLITSX-UHFFFAOYSA-N benzyl N-[2-hydroxy-4-(3-oxomorpholin-4-yl)phenyl]carbamate Chemical compound OC1=C(NC(=O)OCC2=CC=CC=C2)C=CC(=C1)N1CCOCC1=O FFBHFFJDDLITSX-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000005229 chemical vapour deposition Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/02—Use of particular materials as binders, particle coatings or suspension media therefor
- C09K11/025—Use of particular materials as binders, particle coatings or suspension media therefor non-luminescent particle coatings or suspension media
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
- C09K11/08—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
- C09K11/58—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing copper, silver or gold
- C09K11/582—Chalcogenides
- C09K11/584—Chalcogenides with zinc or cadmium
Definitions
- TECHNICAL FIELD This application relates to a process for producing an electroluminescent phosphor, and more particularly, to a process that produces an electroluminescent phosphor with a desired emission spectra.
- Electroluminescent (hereinafter EL) phosphors are used for backlighting in LCD's, in copying machines, for backlighting membrane switches, for automotive dashboard and control switch illumination, for automotive exterior body lighting, for aircraft style information panels, for aircraft information lighting, and for emergency egress lighting.
- EL Electroluminescent
- U.S. Pat. Nos. 3,014,873; 3,076,767; 4,859,361; 5,009,808 and 5,1 10,499 relate to methods for producing EL phosphors. Since EL phosphors are sensitive to moisture it is not uncommon for the phosphors to be coated with a moisture-resistant coating of a metal oxide such as alumina.
- Such coating processes have involved reacting the phosphor, via a chemical vapor deposition process, with a coating agent such as, for example, trimethylaluminum and water vapor.
- a coating agent such as, for example, trimethylaluminum and water vapor.
- An example of such a coated phosphor is shown as Sample Number CJ564 in TABLE I and as CJ30 in TABLE II.
- the phosphor coating in the first instance, contains 4.4 weight percent (hereinafter wgt. %) aluminum, has a Y color coordinate of 0.199 on the C.I.E. Chomaticity Diagram (X value, 0.158) and a half-life of 195 hours and, in the second instance, 4.0 wgt.% aluminum, a Y value of 0.203 and a half-life of 256 hours.
- the half-life refers to that period of time when the brightness of the phosphor decreases to V of its brightness at 24 hours.
- a different coating process having many advantages over the TMA/water process comprises reacting a coating agent such as TMA with an oxygen-ozone mixture.
- This latter process is water-free; however, in some instances this process produces undesired emission changes in the phosphor.
- Even though such phosphors have achieved some commercial success in areas where, for example, brightness might be more desirable than a particular emission spectra, it would be an advance in the art to provide a process for achieving a desired emission spectra in a phosphor having a moisture-sensitizing coating applied by an oxygen-ozone process.
- This invention achieves these and other objectives, in one aspect of the invention, by providing a process for making an electroluminescent phosphor having a given emission spectra A, which comprises the steps of manufacturing a beginning electroluminescent phosphor having an emission spectra B, different than A.
- This beginning phosphor has applied thereto a coating to increase the resistance of the beginning phosphor to the deleterious effects of moisture while simultaneously changing the emission spectra of the beginning phosphor from B to emission spectra A.
- the process is water-free and comprises reacting a coating agent with a coating precursor and a mixture of oxygen and ozone.
- Utilization of this method not only provides a phosphor with a desired emission and moisture protection, but, surprisingly, greatly increases the life.
- This invention provides a process for producing an electroluminescent phosphor that has a commercially desirable emission spectra, moisture protection, long life and high brightness.
- the invention is especially suited for zinc sulfide, copper activated phosphors or other zinc sulfide phosphors where copper is a co-activator, for example, with chlorine.
- control phosphors having Sample Numbers of ELB849, ELB875, and ELB826.
- a process for making an electroluminescent phosphor having a given emission spectra A which comprises first, manufacturing a beginning electroluminescent phosphor having an emission spectra B, different than A.
- This beginning phosphor has applied thereto a coating to increase the resistance of the beginning phosphor to the deleterious effects of moisture while simultaneously changing the emission spectra of the beginning phosphor from B to emission spectra A.
- the process is water-free and comprises reacting a coating agent with a coating precursor and a mixture of oxygen and ozone.
- a beginning ZnS.Cu phosphor was prepared by increasing the normal amount of copper contained therein, from 0.032 wgt.% to 0.039 wgt.% (as determined by atomic absorption analysis). This is a significant increase and raised the Y coordinate to about 0.250 while leaving the X coordinate substantially unaffected.
- the phosphor composition of this invention was prepared from materials as follows:
- the beginning phosphor was produced from the above-cited materials by the standard method of heating the zinc sulfide in a furnace to an elevated temperature in the presence of the copper activator and halide fluxes to achieve an electroluminescent phosphor, cooling the phosphor to ambient temperature and washing the phosphor to remove the flux. The resulting ZnS.Cu phosphor was then dried. Phosphors created by this method are generally known.
- modified Type 813 i.e., a phosphor having an increased amount of
- TABLE II a standard Type 60 0 production lot (CJ30) which is a Type 813 phosphor treated with TMA/H 2 O coating process 1 is included in TABLE II for comparison. While the flow rates of nitrogen through the TMA 2 container were maintained at 0.75 1/minute, rates of nitrogen flow at the bottom of the reactor 3 were kept at a total of 3.75 1/minute. Also, the oxygen/ozone gas mixture was transported 4 into the reaction vessel at a flow rate of 4.6 1/minute. The resulting data on the coated 5 phosphors are shown in TABLE II. 6 TABLE II
- the initial brightness 1 at 24 hours of TH92A (WNE600) lamp was measured at 15 foot lamberts, which is 40% greater than that obtained with the standard CJ30 lot that was prepared by the TMA/H 2 0 process.
- the half-lives of the lamps were enhanced more than 150%, for example, 256 hours with the standard lot CJ30 versus 663 hours with Lot TH92A.
- the greater the amount of aluminum deposit i.e. the greater the coating thickness, the longer the half-life.
- the half-life of TH93 (NE600) with a coating weight of 4.1 % aluminum was estimated at 1295 hours which is about five times the 256 hours of the standard DJ30 lot.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Luminescent Compositions (AREA)
- Electroluminescent Light Sources (AREA)
Abstract
A process for making an electroluminescent phosphor having a given emission spectra A, comprises the steps of manufacturing a beginning electroluminescent phosphor having an emission spectra B, different than A. A coating is applied to the phosphor having the emission spectra B to increase the resistance of the phosphor to the deleterious effects of moisture and change the emission spectra of the phosphor to emission spectra A. The application of the coating includes the steps of reacting a coating precursor with a mixture of oxygen and ozone.
Description
ENCAPSULATED LONG LIFE ELECTROLUMINESCENT PHOSPHOR 5C OSS REFERENCE TO RELATED APPLICATIONS This application claims priority from provisional application S.N. 60/166,619 filed November 19, 1999.
TECHNICAL FIELD This application relates to a process for producing an electroluminescent phosphor, and more particularly, to a process that produces an electroluminescent phosphor with a desired emission spectra.
BACKGROUND ART Electroluminescent (hereinafter EL) phosphors are used for backlighting in LCD's, in copying machines, for backlighting membrane switches, for automotive dashboard and control switch illumination, for automotive exterior body lighting, for aircraft style information panels, for aircraft information lighting, and for emergency egress lighting. U.S. Pat. Nos. 3,014,873; 3,076,767; 4,859,361; 5,009,808 and 5,1 10,499 relate to methods for producing EL phosphors. Since EL phosphors are sensitive to moisture it is not uncommon for the phosphors to be coated with a moisture-resistant coating of a metal oxide such as alumina. Such coating processes have involved reacting the phosphor, via a chemical vapor deposition process, with a coating agent such as, for example, trimethylaluminum and water vapor. An example of such a coated phosphor is shown as Sample Number CJ564 in TABLE I and as CJ30 in TABLE II. The phosphor coating, in the first instance, contains 4.4 weight percent (hereinafter wgt. %) aluminum, has a Y color coordinate of 0.199 on the C.I.E. Chomaticity Diagram (X value, 0.158) and a half-life of 195 hours and, in the second instance, 4.0 wgt.% aluminum, a Y value of 0.203 and a half-life of 256 hours. As used herein the half-life refers to that period of time when the brightness of the phosphor decreases to V of its brightness at 24 hours.
A different coating process having many advantages over the TMA/water process comprises reacting a coating agent such as TMA with an oxygen-ozone mixture. This latter process is water-free; however, in some instances this process produces undesired emission changes in the phosphor. Even though such phosphors have achieved some commercial success in areas where, for example, brightness might be more desirable than a particular emission spectra,
it would be an advance in the art to provide a process for achieving a desired emission spectra in a phosphor having a moisture-sensitizing coating applied by an oxygen-ozone process.
DISCLOSURE OF THE INVENTION
It is, therefore, an object of the present invention to obviate the disadvantages of the prior art.
It is another object of the present invention to produce electroluminescent phosphors having a commercially desirable emission spectra with very long life and high brightness.
This invention achieves these and other objectives, in one aspect of the invention, by providing a process for making an electroluminescent phosphor having a given emission spectra A, which comprises the steps of manufacturing a beginning electroluminescent phosphor having an emission spectra B, different than A. This beginning phosphor has applied thereto a coating to increase the resistance of the beginning phosphor to the deleterious effects of moisture while simultaneously changing the emission spectra of the beginning phosphor from B to emission spectra A. The process is water-free and comprises reacting a coating agent with a coating precursor and a mixture of oxygen and ozone.
Utilization of this method not only provides a phosphor with a desired emission and moisture protection, but, surprisingly, greatly increases the life.
BEST MODE FOR CARRYING OUT THE INVENTION
For a better under understanding of the present invention, together with other and further objectives, advantages and capabilities thereof, reference is made to the following disclosure and appended claims.
This invention provides a process for producing an electroluminescent phosphor that has a commercially desirable emission spectra, moisture protection, long life and high brightness. The invention is especially suited for zinc sulfide, copper activated phosphors or other zinc sulfide phosphors where copper is a co-activator, for example, with chlorine.
Referring now to TABLE I, in addition to the previously mentioned prior art phosphor coated by a TMAΛvater process (Sample Number CJ 564), there are shown control phosphors having Sample Numbers of ELB849, ELB875, and ELB826. These are standard, uncoated, commercially available phosphors (all having essentially the same composition but coming from different lots) having desired color emission with an X coordinate of about 0.160 and a Y coordinate of about 0.200, which provides a blue-green emission. The small variances shown by the color coordinates are well within commercial tolerance specifications.
However, when these materials are coated by the aforementioned oxygen/ozone process a decided color-shift takes place which is represented by a noticeable change in the Y coordinate. These materials are designated, in TABLE I, by Sample Numbers TH54, which is a coated version of ELB849; TH1 1 1, a coated version of ELB875; and TH53 and TH36, which are coated versions of ELB826 differing only in the amount of the coating. Even though the coated materials have increased life and improved brightness, the color-shift makes them unacceptable to many customers.
TABLE I
Accordingly, this problem has been solved by a process for making an electroluminescent
phosphor having a given emission spectra A, which comprises first, manufacturing a beginning electroluminescent phosphor having an emission spectra B, different than A. This beginning phosphor has applied thereto a coating to increase the resistance of the beginning phosphor to the deleterious effects of moisture while simultaneously changing the emission spectra of the beginning phosphor from B to emission spectra A. The process is water-free and comprises reacting a coating agent with a coating precursor and a mixture of oxygen and ozone.
In particular, a beginning ZnS.Cu phosphor was prepared by increasing the normal amount of copper contained therein, from 0.032 wgt.% to 0.039 wgt.% (as determined by atomic absorption analysis). This is a significant increase and raised the Y coordinate to about 0.250 while leaving the X coordinate substantially unaffected.
Generally, the phosphor composition of this invention was prepared from materials as follows:
The beginning phosphor was produced from the above-cited materials by the standard method of heating the zinc sulfide in a furnace to an elevated temperature in the presence of the copper activator and halide fluxes to achieve an electroluminescent phosphor, cooling the phosphor to ambient temperature and washing the phosphor to remove the flux. The resulting ZnS.Cu phosphor was then dried. Phosphors created by this method are generally known. One such phosphor, having 0.032 wgt.% copper, is a Type 813 electroluminescent
1 phosphor (ZnS.Cu) available from Osram Sylvania, Inc., Towanda, PA.
2
**. The phosphor was coated by the method disclosed in co-pending patent application Serial
4 No. 09/585,221, the teachings of which are hereby incoφorated by reference. In particular,
5 two 3.5 kg samples of modified Type 813 (i.e., a phosphor having an increased amount of
6 copper), Lot ELB478-50, (see TABLE II) were treated with trimethylaluminum and
7 oxygen/ozone in a 2" diameter fluid bed at 180°C with variation in the amount of aluminum
8 deposited. During the coating treatment of run TH92, 50 g of a thin-coated sample were
9 collected from the fluid bed reactor and labeled as TH92A. Also, a standard Type 60 0 production lot (CJ30) which is a Type 813 phosphor treated with TMA/H2O coating process 1 is included in TABLE II for comparison. While the flow rates of nitrogen through the TMA 2 container were maintained at 0.75 1/minute, rates of nitrogen flow at the bottom of the reactor 3 were kept at a total of 3.75 1/minute. Also, the oxygen/ozone gas mixture was transported 4 into the reaction vessel at a flow rate of 4.6 1/minute. The resulting data on the coated 5 phosphors are shown in TABLE II. 6 TABLE II
As can bee seen from Table II, the lamp results indicated that the new WNE/TNE/NE600 products made from the modified Type 813 phosphor have significantly better brightness and tremendously longer life than those of current products. For example, the initial brightness 1 at 24 hours of TH92A (WNE600) lamp was measured at 15 foot lamberts, which is 40% greater than that obtained with the standard CJ30 lot that was prepared by the TMA/H20 process. Also, the half-lives of the lamps were enhanced more than 150%, for example, 256
hours with the standard lot CJ30 versus 663 hours with Lot TH92A. As usual, the greater the amount of aluminum deposit, i.e. the greater the coating thickness, the longer the half-life. Most impressively, and surprisingly, the half-life of TH93 (NE600) with a coating weight of 4.1 % aluminum, was estimated at 1295 hours which is about five times the 256 hours of the standard DJ30 lot.
Thus there is provided a process for producing an electroluminescent phosphor with an increased efficiency, great life expectancy and desirable emission spectrum.
While there have been shown and described what are at present considered the preferred embodiments of the invention, it will be apparent to those skilled in the art that various changes and modifications can be made herein without departing from the scope of the invention as defined by the appended claims.
Claims
1. A process for making an electroluminescent phosphor having a given emission spectra A, comprising the steps of: manufacturing a beginning electroluminescent phosphor having an emission spectra B, different than A; applying a coating to said phosphor having said emission spectra B to increase the resistance of said phosphor to the deleterious effects of moisture and change the emission spectra of said phosphor to emission spectra A, said application of said coating including the steps of reacting a coating precursor with a mixture of oxygen and ozone.
2. The process of Claim 1 wherein said emission spectra B has a CIE y value of about 0.250 and said emission spectra A has a CIE y value between 0.230 and about 0.200.
3. The process of Claim 2 wherein said phosphor is a ZnS:Cu and contains about 0.39 Wgt.% copper.
4. The process of Claim 1 wherein said coating precursor is trimethylaluminum.
5. An electroluminescent phosphor created by the process disclosed in claim 1.
6. The electroluminescent phosphor of Claim 5 wherein said phosphor has a half-life of greater than 663 hours.
7. The electroluminescent phosphor of Claim 5 wherein said phosphor has a half-life of about 1295 hours.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16661999P | 1999-11-19 | 1999-11-19 | |
| US166619P | 1999-11-19 | ||
| PCT/US2000/031216 WO2001036559A2 (en) | 1999-11-19 | 2000-11-15 | Encapsulated long life electroluminescent phosphor |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP1412098A2 true EP1412098A2 (en) | 2004-04-28 |
| EP1412098A4 EP1412098A4 (en) | 2008-04-30 |
Family
ID=22604039
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP00978609A Withdrawn EP1412098A4 (en) | 1999-11-19 | 2000-11-15 | Encapsulated long life electroluminescent phosphor |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP1412098A4 (en) |
| JP (1) | JP2003535153A (en) |
| KR (1) | KR100498686B1 (en) |
| CN (1) | CN1256185C (en) |
| AU (1) | AU1605901A (en) |
| CA (1) | CA2381534A1 (en) |
| HU (1) | HUP0500636A3 (en) |
| WO (1) | WO2001036559A2 (en) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6702959B2 (en) * | 1999-11-19 | 2004-03-09 | Osram Sylvania Inc. | Long life, white light emitting electroluminescent phosphor |
| CA2363532A1 (en) * | 2000-12-18 | 2002-06-18 | Osram Sylvania Inc. | Preparation of high-brightness, long life, moisture resistant electroluminescent phosphor |
| US7698842B2 (en) | 2002-01-31 | 2010-04-20 | Volkswagen Ag | Sign, especially a number plate for a motor vehicle |
| US7833437B2 (en) | 2006-01-26 | 2010-11-16 | Global Tungsten & Powders Corp. | Moisture-resistant electroluminescent phosphor with high initial brightness and method of making |
| US8298666B2 (en) * | 2006-01-26 | 2012-10-30 | Global Tungsten & Powders Corp. | Moisture resistant electroluminescent phosphor with high initial brightness and method of making |
| US8011559B2 (en) * | 2009-11-09 | 2011-09-06 | GM Global Technology Operations LLC | Active material-augmented vibration welding system and method of use |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19849581A1 (en) * | 1997-10-27 | 1999-04-29 | Osram Sylvania Inc | Phosphor particles are coated using an inert gas, a coating precursor and an oxygen-ozone mixture |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4585673A (en) * | 1984-05-07 | 1986-04-29 | Gte Laboratories Incorporated | Method for coating phosphor particles |
| US4825124A (en) * | 1984-05-07 | 1989-04-25 | Gte Laboratories Incorporated | Phosphor particle, fluorescent lamp, and manufacturing method |
| US5196234A (en) * | 1986-08-29 | 1993-03-23 | Gte Products Corporation | Method for preparing zinc orthosilicate phosphor particle |
| US5080928A (en) * | 1990-10-05 | 1992-01-14 | Gte Laboratories Incorporated | Method for making moisture insensitive zinc sulfide based luminescent materials |
| EP0560617A3 (en) * | 1992-03-13 | 1993-11-24 | Kawasaki Steel Co | Method of manufacturing insulating film on semiconductor device and apparatus for carrying out the same |
| US5602445A (en) * | 1995-05-12 | 1997-02-11 | Oregon Graduate Institute Of Science And Technology | Blue-violet phosphor for use in electroluminescent flat panel displays |
-
2000
- 2000-11-15 CN CN00815675.1A patent/CN1256185C/en not_active Expired - Fee Related
- 2000-11-15 CA CA002381534A patent/CA2381534A1/en not_active Abandoned
- 2000-11-15 EP EP00978609A patent/EP1412098A4/en not_active Withdrawn
- 2000-11-15 HU HU0500636A patent/HUP0500636A3/en unknown
- 2000-11-15 AU AU16059/01A patent/AU1605901A/en not_active Abandoned
- 2000-11-15 KR KR10-2002-7000918A patent/KR100498686B1/en not_active IP Right Cessation
- 2000-11-15 WO PCT/US2000/031216 patent/WO2001036559A2/en active IP Right Grant
- 2000-11-15 JP JP2001539040A patent/JP2003535153A/en active Pending
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19849581A1 (en) * | 1997-10-27 | 1999-04-29 | Osram Sylvania Inc | Phosphor particles are coated using an inert gas, a coating precursor and an oxygen-ozone mixture |
Non-Patent Citations (1)
| Title |
|---|
| See also references of WO0136559A2 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2001036559A3 (en) | 2004-02-26 |
| CA2381534A1 (en) | 2001-05-25 |
| HUP0500636A3 (en) | 2008-05-28 |
| EP1412098A4 (en) | 2008-04-30 |
| KR100498686B1 (en) | 2005-07-01 |
| KR20020062913A (en) | 2002-07-31 |
| CN1256185C (en) | 2006-05-17 |
| HUP0500636A2 (en) | 2005-10-28 |
| AU1605901A (en) | 2001-05-30 |
| CN1531466A (en) | 2004-09-22 |
| JP2003535153A (en) | 2003-11-25 |
| WO2001036559A2 (en) | 2001-05-25 |
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