DE2853411C2 - - Google Patents
Info
- Publication number
- DE2853411C2 DE2853411C2 DE2853411A DE2853411A DE2853411C2 DE 2853411 C2 DE2853411 C2 DE 2853411C2 DE 2853411 A DE2853411 A DE 2853411A DE 2853411 A DE2853411 A DE 2853411A DE 2853411 C2 DE2853411 C2 DE 2853411C2
- Authority
- DE
- Germany
- Prior art keywords
- tube
- lever
- bis
- component
- anthracene
- 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
- ZHBOFZNNPZNWGB-UHFFFAOYSA-N 9,10-bis(phenylethynyl)anthracene Chemical compound C1=CC=CC=C1C#CC(C1=CC=CC=C11)=C(C=CC=C2)C2=C1C#CC1=CC=CC=C1 ZHBOFZNNPZNWGB-UHFFFAOYSA-N 0.000 claims description 21
- 239000011521 glass Substances 0.000 claims description 21
- 239000003085 diluting agent Substances 0.000 claims description 18
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 claims description 16
- 150000002978 peroxides Chemical class 0.000 claims description 15
- 239000003708 ampul Substances 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 8
- MWPLVEDNUUSJAV-UHFFFAOYSA-N anthracene Chemical compound C1=CC=CC2=CC3=CC=CC=C3C=C21 MWPLVEDNUUSJAV-UHFFFAOYSA-N 0.000 claims description 7
- 239000000463 material Substances 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 3
- 230000001154 acute effect Effects 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 35
- -1 polyethylene Polymers 0.000 description 22
- 239000000243 solution Substances 0.000 description 21
- DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical compound CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 18
- 239000000203 mixture Substances 0.000 description 17
- 238000005452 bending Methods 0.000 description 11
- NIQCNGHVCWTJSM-UHFFFAOYSA-N Dimethyl phthalate Chemical compound COC(=O)C1=CC=CC=C1C(=O)OC NIQCNGHVCWTJSM-UHFFFAOYSA-N 0.000 description 10
- 239000004698 Polyethylene Substances 0.000 description 10
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 10
- 229920000573 polyethylene Polymers 0.000 description 10
- 238000006243 chemical reaction Methods 0.000 description 9
- 239000002904 solvent Substances 0.000 description 8
- IMMCAKJISYGPDQ-UHFFFAOYSA-N 1-chloro-9,10-bis(phenylethynyl)anthracene Chemical compound C12=CC=CC=C2C(C#CC=2C=CC=CC=2)=C2C(Cl)=CC=CC2=C1C#CC1=CC=CC=C1 IMMCAKJISYGPDQ-UHFFFAOYSA-N 0.000 description 7
- 238000000034 method Methods 0.000 description 7
- 229910000831 Steel Inorganic materials 0.000 description 6
- 239000010959 steel Substances 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 5
- TZZLVFUOAYMTHA-UHFFFAOYSA-N bis-(2,4,5-trichloro-6-(pentyloxycarbonyl)phenyl)oxalate Chemical compound CCCCCOC(=O)C1=C(Cl)C(Cl)=CC(Cl)=C1OC(=O)C(=O)OC1=C(Cl)C=C(Cl)C(Cl)=C1C(=O)OCCCCC TZZLVFUOAYMTHA-UHFFFAOYSA-N 0.000 description 5
- 150000001875 compounds Chemical class 0.000 description 5
- FBSAITBEAPNWJG-UHFFFAOYSA-N dimethyl phthalate Natural products CC(=O)OC1=CC=CC=C1OC(C)=O FBSAITBEAPNWJG-UHFFFAOYSA-N 0.000 description 5
- 229960001826 dimethylphthalate Drugs 0.000 description 5
- 239000007850 fluorescent dye Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- YDYTTZZBQVZTPY-UHFFFAOYSA-N 2-chloro-9,10-bis(phenylethynyl)anthracene Chemical compound C=12C=CC=CC2=C(C#CC=2C=CC=CC=2)C2=CC(Cl)=CC=C2C=1C#CC1=CC=CC=C1 YDYTTZZBQVZTPY-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- ABBQHOQBGMUPJH-UHFFFAOYSA-M Sodium salicylate Chemical compound [Na+].OC1=CC=CC=C1C([O-])=O ABBQHOQBGMUPJH-UHFFFAOYSA-M 0.000 description 4
- 230000004913 activation Effects 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 229960004025 sodium salicylate Drugs 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 150000003901 oxalic acid esters Chemical class 0.000 description 3
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- MTZQAGJQAFMTAQ-UHFFFAOYSA-N ethyl benzoate Chemical compound CCOC(=O)C1=CC=CC=C1 MTZQAGJQAFMTAQ-UHFFFAOYSA-N 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000002347 injection Methods 0.000 description 2
- 239000007924 injection Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- XZKOELJOFVHXRS-UHFFFAOYSA-N 1,1,1,2,2,3,3-heptafluoro-3-(1,1,2,2,3,3,3-heptafluoropropoxy)propane Chemical compound FC(F)(F)C(F)(F)C(F)(F)OC(F)(F)C(F)(F)C(F)(F)F XZKOELJOFVHXRS-UHFFFAOYSA-N 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
- DCCXNTCSVXAHAN-UHFFFAOYSA-N 1,5-dichloro-9,10-bis(2-phenylethynyl)anthracene Chemical compound C12=C(Cl)C=CC=C2C(C#CC=2C=CC=CC=2)=C2C(Cl)=CC=CC2=C1C#CC1=CC=CC=C1 DCCXNTCSVXAHAN-UHFFFAOYSA-N 0.000 description 1
- YONGNHJIWAYNLC-UHFFFAOYSA-N 1,8-dichloro-9,10-bis(2-phenylethynyl)anthracene Chemical compound C12=CC=CC(Cl)=C2C(C#CC=2C=CC=CC=2)=C2C(Cl)=CC=CC2=C1C#CC1=CC=CC=C1 YONGNHJIWAYNLC-UHFFFAOYSA-N 0.000 description 1
- GWGADDLVYCILFS-UHFFFAOYSA-N 1-bromo-9,10-bis(2-phenylethynyl)anthracene Chemical compound C12=CC=CC=C2C(C#CC=2C=CC=CC=2)=C2C(Br)=CC=CC2=C1C#CC1=CC=CC=C1 GWGADDLVYCILFS-UHFFFAOYSA-N 0.000 description 1
- YCKSJJIBZGMBEH-UHFFFAOYSA-N 1-fluoro-9,10-bis(2-phenylethynyl)anthracene Chemical compound C12=CC=CC=C2C(C#CC=2C=CC=CC=2)=C2C(F)=CC=CC2=C1C#CC1=CC=CC=C1 YCKSJJIBZGMBEH-UHFFFAOYSA-N 0.000 description 1
- LBPLCAZHVAZWNT-UHFFFAOYSA-N 1-methyl-9,10-bis(2-phenylethynyl)anthracene Chemical compound C12=CC=CC=C2C(C#CC=2C=CC=CC=2)=C2C(C)=CC=CC2=C1C#CC1=CC=CC=C1 LBPLCAZHVAZWNT-UHFFFAOYSA-N 0.000 description 1
- AOPDRZXCEAKHHW-UHFFFAOYSA-N 1-pentoxypentane Chemical compound CCCCCOCCCCC AOPDRZXCEAKHHW-UHFFFAOYSA-N 0.000 description 1
- WEFYTUJDZBLKSR-UHFFFAOYSA-N 5-(2-hydroxyethoxymethyl)nonan-5-ol Chemical compound CCCCC(O)(CCCC)COCCO WEFYTUJDZBLKSR-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 description 1
- BMWRQJKETXKDFV-UHFFFAOYSA-N C(=O)(OC)C1=CC=CC=C1C=1C(=C(C=C(C1Cl)Cl)OC(C(=O)OC1=C(C(=C(C(=C1)Cl)Cl)C1=CC=CC=C1C(=O)OC)Cl)=O)Cl Chemical compound C(=O)(OC)C1=CC=CC=C1C=1C(=C(C=C(C1Cl)Cl)OC(C(=O)OC1=C(C(=C(C(=C1)Cl)Cl)C1=CC=CC=C1C(=O)OC)Cl)=O)Cl BMWRQJKETXKDFV-UHFFFAOYSA-N 0.000 description 1
- CRRVZGNHULMCLN-UHFFFAOYSA-N C(=O)(OCCCCC)C1=CC=CC=C1C1=C(C(=C(C=C1Cl)OC(C(=O)OC1=C(C(=C(C(=C1)Cl)C1=CC=CC=C1C(=O)OCCCCC)Cl)Cl)=O)Cl)Cl Chemical compound C(=O)(OCCCCC)C1=CC=CC=C1C1=C(C(=C(C=C1Cl)OC(C(=O)OC1=C(C(=C(C(=C1)Cl)C1=CC=CC=C1C(=O)OCCCCC)Cl)Cl)=O)Cl)Cl CRRVZGNHULMCLN-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- PURKHUDOTFUVNG-UHFFFAOYSA-N bis(2,3,5-trichloro-6-pentoxycarbonylphenyl) oxalate Chemical compound CCCCCOC(=O)C1=C(Cl)C=C(Cl)C(Cl)=C1OC(=O)C(=O)OC1=C(Cl)C(Cl)=CC(Cl)=C1C(=O)OCCCCC PURKHUDOTFUVNG-UHFFFAOYSA-N 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- MEWGFPPXDVFAOH-UHFFFAOYSA-N bis[2,4,5-trichloro-3-(2-pentoxycarbonylphenyl)phenyl] oxalate Chemical compound C(=O)(OCCCCC)C1=CC=CC=C1C=1C(=C(C=C(C1Cl)Cl)OC(C(=O)OC1=C(C(=C(C(=C1)Cl)Cl)C1=CC=CC=C1C(=O)OCCCCC)Cl)=O)Cl MEWGFPPXDVFAOH-UHFFFAOYSA-N 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 238000007667 floating Methods 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 239000012778 molding material Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- XCRBXWCUXJNEFX-UHFFFAOYSA-N peroxybenzoic acid Chemical compound OOC(=O)C1=CC=CC=C1 XCRBXWCUXJNEFX-UHFFFAOYSA-N 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 230000011664 signaling Effects 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- PFUVRDFDKPNGAV-UHFFFAOYSA-N sodium peroxide Chemical compound [Na+].[Na+].[O-][O-] PFUVRDFDKPNGAV-UHFFFAOYSA-N 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 230000003595 spectral effect Effects 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F21—LIGHTING
- F21K—NON-ELECTRIC LIGHT SOURCES USING LUMINESCENCE; LIGHT SOURCES USING ELECTROCHEMILUMINESCENCE; LIGHT SOURCES USING CHARGES OF COMBUSTIBLE MATERIAL; LIGHT SOURCES USING SEMICONDUCTOR DEVICES AS LIGHT-GENERATING ELEMENTS; LIGHT SOURCES NOT OTHERWISE PROVIDED FOR
- F21K2/00—Non-electric light sources using luminescence; Light sources using electrochemiluminescence
- F21K2/06—Non-electric light sources using luminescence; Light sources using electrochemiluminescence using chemiluminescence
-
- 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
-
- 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)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electromagnetism (AREA)
- General Engineering & Computer Science (AREA)
- Luminescent Compositions (AREA)
- Investigating Or Analysing Materials By The Use Of Chemical Reactions (AREA)
- Vessels And Coating Films For Discharge Lamps (AREA)
- Manufacture Of Tobacco Products (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US86177177A | 1977-12-19 | 1977-12-19 | |
| US05/861,772 US4186426A (en) | 1977-12-19 | 1977-12-19 | Emergency lighting device |
| US88812678A | 1978-03-20 | 1978-03-20 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE2853411A1 DE2853411A1 (de) | 1979-08-23 |
| DE2853411C2 true DE2853411C2 (enrdf_load_stackoverflow) | 1988-07-14 |
Family
ID=27420415
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19782853411 Granted DE2853411A1 (de) | 1977-12-19 | 1978-12-11 | Chemischer leuchtstab |
Country Status (13)
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5757992U (enrdf_load_stackoverflow) * | 1980-09-22 | 1982-04-05 | ||
| JPS5757989U (enrdf_load_stackoverflow) * | 1980-09-22 | 1982-04-05 | ||
| JPS5757991U (enrdf_load_stackoverflow) * | 1980-09-22 | 1982-04-05 | ||
| JPS5757990U (enrdf_load_stackoverflow) * | 1980-09-22 | 1982-04-05 | ||
| US4379320A (en) * | 1981-02-19 | 1983-04-05 | American Cyanamid Company | Chemical lighting device |
| US4751616A (en) * | 1987-01-07 | 1988-06-14 | American Cyanamid Company | Double reverse chemiluminescent lighting device |
| DE3824772A1 (de) * | 1988-02-26 | 1989-08-31 | Noggerath Geb | Behaeltnis zur aufnahme von notfall-geraeten |
| US5277173A (en) * | 1992-10-09 | 1994-01-11 | Fred Cantele | Chemiluminiscent disposable laryngoscope |
| JP3595642B2 (ja) * | 1997-02-25 | 2004-12-02 | 能美防災株式会社 | 非常用ライト |
| WO1999016342A1 (fr) * | 1997-09-29 | 1999-04-08 | Laboratoires Piette International S.A. | Element d'eclairage pour examen medical photographique ou visuel |
| US7083294B2 (en) * | 2004-02-18 | 2006-08-01 | Steinberg Benjamin H | Reusable and rechargeable glow device |
| WO2005103196A1 (ja) * | 2004-04-27 | 2005-11-03 | Lumica Corporation | 化学発光組成物 |
| US7617776B1 (en) * | 2004-09-27 | 2009-11-17 | Diffraction, Ltd. | Selective emitting flare nanosensors |
| US20100014275A1 (en) * | 2008-07-21 | 2010-01-21 | Earl Cranor | End cap attachment for chemiluminescent light sticks |
| US20130168620A1 (en) * | 2011-12-30 | 2013-07-04 | Maggilume, LLC | Chemiluminescent system |
| JP6621120B2 (ja) * | 2017-01-16 | 2019-12-25 | 株式会社ルミカ | 化学発光体および化学発光システム、ならびに化学発光体用破割性容器、化学発光用酸化液 |
| DE202020104444U1 (de) | 2020-07-31 | 2020-08-11 | SCHMIETEX ENGINEERING GmbH | Aktivierbare chemische Lichtquelle |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3557233A (en) * | 1968-03-14 | 1971-01-19 | American Cyanamid Co | Aromatic hydrocarbons substituted by phenylethynyl groups |
| DE2029899A1 (de) * | 1970-06-18 | 1971-12-30 | Deutsche Gold- Und Silber-Scheideanstalt Vormals Roessler, 6000 Frankfurt | Verfahren zum Vernetzen von Füllstoffen enthaltendem natürlichem und synthetischem Kautschuk bzw. diese enthaltenden Mischungen |
| US3691085A (en) * | 1970-07-13 | 1972-09-12 | American Cyanamid Co | Method of controlling the lifetime of oxalate ester chemiluminescent reactions |
| US3704231A (en) * | 1971-02-16 | 1972-11-28 | American Cyanamid Co | Chemiluminescent additives |
| US3749679A (en) * | 1971-03-15 | 1973-07-31 | American Cyanamid Co | Carboalkoxy substituted bis-phenyl oxalates as superior chemiluminescent materials |
| US3888786A (en) * | 1972-06-12 | 1975-06-10 | American Cyanamid Co | Chlorinated bis(phenylethynyl)anthracenes as fluorescers in chemiluminescent systems |
| CA1015555A (en) * | 1972-06-12 | 1977-08-16 | American Cyanamid Company | Chlorinated bis(phenylethynyl)anthracenes as fluorescers in chemiluminescent systems |
| US3764796A (en) * | 1972-10-05 | 1973-10-09 | Us Navy | Chemical lighting device |
| US3819925A (en) * | 1973-03-12 | 1974-06-25 | Us Navy | Chemiluminescent device |
| US3900728A (en) * | 1973-04-13 | 1975-08-19 | Gordon B Holcombe | Hand held device for activating a chemiluminescent wand |
| US3813534A (en) * | 1973-09-14 | 1974-05-28 | Us Navy | Chemical lighting device having interlocking ampoules |
| JPS5114778A (ja) * | 1974-07-22 | 1976-02-05 | Bii Horukuumu Goodon | Kagakureikohatsuseibookatsuseikasuru sochi |
-
1978
- 1978-10-03 GR GR57362A patent/GR72790B/el unknown
- 1978-10-09 AU AU40518/78A patent/AU4051878A/en active Pending
- 1978-10-17 GB GB7840913A patent/GB2013704B/en not_active Expired
- 1978-10-25 AR AR274222A patent/AR221068A1/es active
- 1978-11-03 NL NL7810989A patent/NL7810989A/xx not_active Application Discontinuation
- 1978-11-17 NO NO783878A patent/NO147278C/no unknown
- 1978-11-28 BR BR7807812A patent/BR7807812A/pt unknown
- 1978-12-11 DE DE19782853411 patent/DE2853411A1/de active Granted
- 1978-12-18 CH CH1283978A patent/CH636939A5/de not_active IP Right Cessation
- 1978-12-18 SE SE7813006A patent/SE7813006L/xx unknown
- 1978-12-18 IT IT52330/78A patent/IT1111055B/it active
- 1978-12-19 FR FR7835675A patent/FR2412029A1/fr active Granted
- 1978-12-19 JP JP15679178A patent/JPS5491982A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6232234B2 (enrdf_load_stackoverflow) | 1987-07-13 |
| DE2853411A1 (de) | 1979-08-23 |
| AR221068A1 (es) | 1980-12-30 |
| NO147278C (no) | 1983-03-09 |
| JPS5491982A (en) | 1979-07-20 |
| IT7852330A0 (it) | 1978-12-18 |
| GB2013704B (en) | 1982-05-19 |
| AU4051878A (en) | 1980-04-17 |
| CH636939A5 (de) | 1983-06-30 |
| GB2013704A (en) | 1979-08-15 |
| NO147278B (no) | 1982-11-29 |
| SE7813006L (sv) | 1979-06-20 |
| BR7807812A (pt) | 1979-07-31 |
| GR72790B (enrdf_load_stackoverflow) | 1983-12-05 |
| FR2412029A1 (fr) | 1979-07-13 |
| NO783878L (no) | 1979-06-20 |
| IT1111055B (it) | 1986-01-13 |
| NL7810989A (nl) | 1979-06-21 |
| FR2412029B1 (enrdf_load_stackoverflow) | 1983-03-11 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| D2 | Grant after examination | ||
| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |