WO1996030461A1 - Solution chimiluminescente amelioree - Google Patents
Solution chimiluminescente amelioree Download PDFInfo
- Publication number
- WO1996030461A1 WO1996030461A1 PCT/BE1996/000034 BE9600034W WO9630461A1 WO 1996030461 A1 WO1996030461 A1 WO 1996030461A1 BE 9600034 W BE9600034 W BE 9600034W WO 9630461 A1 WO9630461 A1 WO 9630461A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- solution
- polymer
- rubrene
- red
- solution according
- Prior art date
Links
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
- C09K11/06—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials
- C09K11/07—Luminescent, e.g. electroluminescent, chemiluminescent materials containing organic luminescent materials having chemically interreactive components, e.g. reactive chemiluminescent compositions
Definitions
- the present invention relates to a particular improvement to the solutions and methods used to obtain light from well-known phenomena relating to chemiluminescence based on the use of peroxyoxalate.
- Chemiluminescence based on the reaction of a peroxyoxalate with hydrogen peroxide and a fluorescent dye is a classic technique that has been widely developed.
- the oxalate is trichloropentoxyphenyl oxalate in an organic solvent, a catalyst being provided in the hydrogen peroxide solution which will be mixed with the oxalate-dye system when the chemiluminescence reaction is to start.
- the most frequently used fluorescent dyes to date are phenylethynylantracene (and its chlorine derivatives) which produce green or yellow-green chemiluminescence, diphenylantracene and its chlorine derivatives, which provide blue or indigo chemiluminescence, and certain derivatives perylene which lead to red or pink chemiluminescence.
- rubrene dye tetraphenylnaphthacene
- rubrene dye lacks stability and rapid degradation is observed in the presence of hydrogen peroxide, which is necessarily added to initiate the chemiluminescence reaction.
- the initial luminosity is therefore not essentially greater than that observed with the dye without polymer, but on the other hand said luminosity, according to the invention, mc-intient for a much longer duration, comparable to calle observed with conventional dyes. We thus pass from an emission duration of a few tens of minutes to several hours, the orange color being maintained.
- the reaction can continue until the oxalate is completely consumed.
- the polymer according to the invention therefore essentially exerts a protective effect against the degradation of rubrene by hydrogen peroxide while this effect is not necessary for the other fluorescent agents.
- the molecular weight of the polyoxyethylene polymer (or polyethylene glycols) will be between 1,000 and 1,000,000, more preferably 50,000 and 300,000.
- the polymer is advantageously present in an amount equivalent to 0.05 to 5% by weight, more particularly from 0.1 to 1%.
- a particularly suitable polymer is polyoxyethylene with an average molecular weight of around 200,000.
- the invention also includes, for said rubrene solutions, means for enhancing the stable chemiluminescence thus obtained, by giving it a color the emission of which is in red-orange, instead of orange. It is well known that the market demand for red chemiluminescence is not sufficiently met.
- Such solid powder solutions are known in the trade: they emit red fluorescence under the action of daylight or any other common lighting.
- the dyes found there have no property of emitting a usable fluorescence such as which in chemiluminescent reactions to peroxyoxalates, otherwise they would have been used for a long time for this purpose.
- Their commercial use in solid solution in polymers ground to emit in the red under the action of ambient light has always been done so far by their incorporation in varnishes, paints, inks, plastic molding materials or other mediums of this genre.
- these solid powder solutions are not used as usual. They do not receive lighting. Suspended in the liquid chemiluminescence substrate, they receive here only the orange chemiluminescent emission which surrounds them, coming from the rubrene, and we note that they re-emit in red with an intensity such as the resulting tint in the eyes of the The observer is a very intense red-orange, and no longer an orange, as with the rubrene alone.
- the powders which can be used according to the invention are varied but the polymers concerned will most often be resins of the urea-formaldehyde, melamine-formaldehyde, sulfonamide, glycerophthalate, vinyl, acrylic, acrylonitrile or polyester type.
- the red fluorescent dyes (generally present at concentrations e.g. 1 to 6% by weight) dissolved in these resins are advantageously chosen from xanthenes, coumarins and naphthalimides. These powders are commercially available and produced in Europe, Canada, the United States and Japan. These powders generally have a particle size between 1 and 25 micrometers. Their solubility in the solvents generally used as chemiluminescent reaction supports such as dibutyl phthalate, dimethyl phthalate, or butyl benzoate, is low e.g. less than 4 grams per liter. For the invention, therefore, a suspension is used, making sure to use these powders with a sufficiently fine particle size to avoid sedimentation of the -ilaborate product.
- Radiant-Magruder TI P, JS, R, K, MP U.Min & Chem. Co FG, FB, NP, FC, FH, FAE
- a mixture of 80 parts by volume of dimethylphthalate and 20 parts of t-butanol is also prepared, in which 25 g of hydrogen peroxide and 60 mg of potassium salicylate are dissolved; this solution constituting the activator.
- chemiluminescence 1 part by volume of activator is mixed at room temperature with 3 parts of colored solution in a common borosilicate glass container, preferably a beaker of approximately 50 ml.
- a common borosilicate glass container preferably a beaker of approximately 50 ml.
- Example 2 an activator solution of identical composition is also prepared and the chemiluminescence reaction is initiated by mixing the two solutions in the same proportion from 1 to 3.
- Example 1 an activator solution of identical composition is also prepared and the chemiluminescence reaction is initiated by mixing the two solutions in the same proportion from 1 to 3, and again, comparative observations are made, in having taken care, here again, to work in identical transparent containers.
- the difference in color compared to that of Examples 1 and 2 is in any case certain in the direction of a shift towards the red.
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP8528721A JPH11502553A (ja) | 1995-03-31 | 1996-03-26 | 改良された化学ルミネセンス溶液 |
US08/945,402 US5824242A (en) | 1995-03-31 | 1996-03-26 | Chemiluminescent solution |
DE69609600T DE69609600T2 (de) | 1995-03-31 | 1996-03-26 | Verbesserte chemilumineszente lösung |
EP96908931A EP0817820B1 (fr) | 1995-03-31 | 1996-03-26 | Solution chimiluminescente amelioree |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE9500289 | 1995-03-31 | ||
BE9500289A BE1009224A6 (fr) | 1995-03-31 | 1995-03-31 | Solution chimiluminescente amelioree. |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1996030461A1 true WO1996030461A1 (fr) | 1996-10-03 |
Family
ID=3888889
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/BE1996/000034 WO1996030461A1 (fr) | 1995-03-31 | 1996-03-26 | Solution chimiluminescente amelioree |
Country Status (6)
Country | Link |
---|---|
US (1) | US5824242A (fr) |
EP (1) | EP0817820B1 (fr) |
JP (1) | JPH11502553A (fr) |
BE (1) | BE1009224A6 (fr) |
DE (1) | DE69609600T2 (fr) |
WO (1) | WO1996030461A1 (fr) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7028687B1 (en) | 1999-08-26 | 2006-04-18 | Precious Life, Llc | Escape hood |
US6267914B1 (en) * | 1999-11-02 | 2001-07-31 | Omniglow Corporation | Variable chemiluminescent process and product |
WO2002002401A1 (fr) | 2000-06-29 | 2002-01-10 | The Night Fun Co. | Dispositif eclaire de signal d'alarme et ballon volant |
US20050288808A1 (en) * | 2004-06-14 | 2005-12-29 | Lopez George A | Computer system for efficient design and manufacture of multiple-component devices |
US20060214141A1 (en) * | 2005-03-23 | 2006-09-28 | Yankielun Norbert E | Luminescent illumination adjunct for night vision |
US20080157039A1 (en) * | 2006-12-30 | 2008-07-03 | Matthew Mark Zuckerman | Nano-polymeric encapsulation of a key reactant to control chemo-fluorescent active reaction period for chemiluminescent paint |
CN101240165B (zh) * | 2007-02-07 | 2012-05-02 | 天津天龙化学发光管有限公司 | 一种草酸酯化学发光体系 |
US20090166595A1 (en) * | 2007-08-01 | 2009-07-02 | Chemical Light, Inc. | Enhanced chemiluminescent lighting formulation and element |
CA2731729C (fr) * | 2008-07-23 | 2016-11-01 | Cyalume Technologies, Inc. | Systeme chimioluminescent activable sous pression utile pour convertir une detection d'intrusion |
WO2012101848A1 (fr) * | 2011-01-27 | 2012-08-02 | 株式会社ルミカ | Liquide oxydant pour élément chimioluminescent et système chimioluminescent le contenant |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0175889A1 (fr) * | 1984-09-24 | 1986-04-02 | American Cyanamid Company | Utilisation de polymères solubles dans l'eau pour les compositions aqueuses chimioluminescentes |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3994820A (en) * | 1972-06-19 | 1976-11-30 | American Cyanamid Company | Polymers in oxalate chemiluminescent systems |
US4016133A (en) * | 1974-03-18 | 1977-04-05 | Sinloihi Co. | Fluorescent colored resin particles and process for preparation thereof |
US4379320A (en) * | 1981-02-19 | 1983-04-05 | American Cyanamid Company | Chemical lighting device |
US4859369A (en) * | 1984-09-24 | 1989-08-22 | American Cyanamid Company | Use of water-soluble polymers in aqueous chemical light formulations |
US4911830A (en) * | 1988-05-26 | 1990-03-27 | Pms Consolidated | Fluorescent pigment concentrates |
BE1002483A6 (fr) * | 1989-06-20 | 1991-02-26 | Continental Photo | Solution chimiluminescente a base de perylene substitue. |
US5173218A (en) * | 1990-12-24 | 1992-12-22 | American Cyanamid Company | Preparation of chemiluminescent vinyl halide or vinylidene halide polymer structures |
-
1995
- 1995-03-31 BE BE9500289A patent/BE1009224A6/fr not_active IP Right Cessation
-
1996
- 1996-03-26 EP EP96908931A patent/EP0817820B1/fr not_active Expired - Lifetime
- 1996-03-26 JP JP8528721A patent/JPH11502553A/ja active Pending
- 1996-03-26 DE DE69609600T patent/DE69609600T2/de not_active Expired - Fee Related
- 1996-03-26 US US08/945,402 patent/US5824242A/en not_active Expired - Lifetime
- 1996-03-26 WO PCT/BE1996/000034 patent/WO1996030461A1/fr active IP Right Grant
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0175889A1 (fr) * | 1984-09-24 | 1986-04-02 | American Cyanamid Company | Utilisation de polymères solubles dans l'eau pour les compositions aqueuses chimioluminescentes |
Also Published As
Publication number | Publication date |
---|---|
US5824242A (en) | 1998-10-20 |
JPH11502553A (ja) | 1999-03-02 |
DE69609600D1 (de) | 2000-09-07 |
EP0817820A1 (fr) | 1998-01-14 |
BE1009224A6 (fr) | 1997-01-07 |
DE69609600T2 (de) | 2001-05-03 |
EP0817820B1 (fr) | 2000-08-02 |
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