GB1067607A - Chemiluminescent compositions - Google Patents
Chemiluminescent compositionsInfo
- Publication number
- GB1067607A GB1067607A GB4774365A GB4774365A GB1067607A GB 1067607 A GB1067607 A GB 1067607A GB 4774365 A GB4774365 A GB 4774365A GB 4774365 A GB4774365 A GB 4774365A GB 1067607 A GB1067607 A GB 1067607A
- Authority
- GB
- United Kingdom
- Prior art keywords
- substituted
- fluorescent
- anhydride
- isocyanate
- hydroperoxide
- 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.)
- Expired
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
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
A chemiluminescent composition comprises (1) a dicarboxylic acid of formula COOH.(CO)m.(COHOH)m.COOH where m and n are less than 11, (2) an anhydrous hydroperoxide, (3) a specified dehydrating agent, and (4) a fluorescent compound; the fluorescent compound may be omitted if one of the other constituents is itself fluorescent. The dehydrating agent may be (a) a carbodiimide RN=C=NR1 where R and R1 are (normal or substituted) alkyl (C1-C16), aryl, cycloalkyl, heterocyclic, substituted alkyl, substituted aryl, substituted cycloalkyl or substituted heterocyclic, (b) an anhydride of carboxylic acid, (c) an isocyanate, (d) an anhydride of R-substituted carboxylic acid (R as above), or (e) an R-substituted isocyanate. The hydroperoxide may be H2O2 or a perhydrate. The materials may be present in a liquid diluent, or the blended solids may be stored, a diluent being added to initiate the reaction. The reaction may also be initiated by friction, or by the addition of any one component, other than the fluorescent component, to a mixture of the others. One or more components may be contained in, e.g. a dissolvable capsule before use. Light output may be improved by the addition of a small amount of an anhydrous acid catalyst; many examples of suitable organic and inorganic acids are given. Fluorescent materials mentioned, emitting between 330 and 700 millimicron, include anthracenes, anthrenes, naphthacenes, stilbenes etc.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB4774365A GB1067607A (en) | 1965-11-10 | 1965-11-10 | Chemiluminescent compositions |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB4774365A GB1067607A (en) | 1965-11-10 | 1965-11-10 | Chemiluminescent compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1067607A true GB1067607A (en) | 1967-05-03 |
Family
ID=10446100
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4774365A Expired GB1067607A (en) | 1965-11-10 | 1965-11-10 | Chemiluminescent compositions |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1067607A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4313843A (en) * | 1974-04-26 | 1982-02-02 | American Cyanamid Company | Superior oxalate ester chemical lighting system |
| WO1982002899A1 (en) * | 1981-02-26 | 1982-09-02 | Cyanamid Co American | Sulfonated rubrene and aqueous chemiluminescent compositions containing the same |
-
1965
- 1965-11-10 GB GB4774365A patent/GB1067607A/en not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4313843A (en) * | 1974-04-26 | 1982-02-02 | American Cyanamid Company | Superior oxalate ester chemical lighting system |
| WO1982002899A1 (en) * | 1981-02-26 | 1982-09-02 | Cyanamid Co American | Sulfonated rubrene and aqueous chemiluminescent compositions containing the same |
| US4366079A (en) * | 1981-02-26 | 1982-12-28 | American Cyanamid Company | Sulfonated rubrene and aqueous chemiluminescent compositions containing the same |
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