EP0752900A1 - Procedes et compositions d'extinction des incendies sans danger pour la couche d'ozone - Google Patents
Procedes et compositions d'extinction des incendies sans danger pour la couche d'ozoneInfo
- Publication number
- EP0752900A1 EP0752900A1 EP95913781A EP95913781A EP0752900A1 EP 0752900 A1 EP0752900 A1 EP 0752900A1 EP 95913781 A EP95913781 A EP 95913781A EP 95913781 A EP95913781 A EP 95913781A EP 0752900 A1 EP0752900 A1 EP 0752900A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- fire
- extinguishing
- composition
- compositions
- acid
- 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- Withdrawn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
- 239000000203 mixture Substances 0.000 title claims abstract description 39
- 238000000034 method Methods 0.000 title claims abstract description 29
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 title description 9
- 229910001508 alkali metal halide Inorganic materials 0.000 claims abstract description 6
- 150000008045 alkali metal halides Chemical class 0.000 claims abstract description 6
- 239000003921 oil Substances 0.000 claims abstract description 6
- 150000003505 terpenes Chemical class 0.000 claims abstract description 6
- 235000007586 terpenes Nutrition 0.000 claims abstract description 6
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 claims abstract description 4
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims abstract description 4
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 claims abstract description 4
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 claims abstract description 4
- 239000004202 carbamide Substances 0.000 claims abstract description 4
- 235000019837 monoammonium phosphate Nutrition 0.000 claims abstract description 4
- 239000006012 monoammonium phosphate Substances 0.000 claims abstract description 4
- 235000019198 oils Nutrition 0.000 claims abstract description 4
- 229910000028 potassium bicarbonate Inorganic materials 0.000 claims abstract description 4
- 235000015497 potassium bicarbonate Nutrition 0.000 claims abstract description 4
- 239000011736 potassium bicarbonate Substances 0.000 claims abstract description 4
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 claims abstract description 4
- 150000001875 compounds Chemical class 0.000 claims description 9
- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- 239000000654 additive Substances 0.000 abstract description 13
- 230000000996 additive effect Effects 0.000 abstract description 9
- 239000002253 acid Substances 0.000 abstract description 3
- 230000002000 scavenging effect Effects 0.000 abstract description 2
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 150000002430 hydrocarbons Chemical class 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 description 25
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 9
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 8
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 8
- 229910052794 bromium Inorganic materials 0.000 description 8
- YFMFNYKEUDLDTL-UHFFFAOYSA-N 1,1,1,2,3,3,3-heptafluoropropane Chemical compound FC(F)(F)C(F)C(F)(F)F YFMFNYKEUDLDTL-UHFFFAOYSA-N 0.000 description 6
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- XPDWGBQVDMORPB-UHFFFAOYSA-N Fluoroform Chemical compound FC(F)F XPDWGBQVDMORPB-UHFFFAOYSA-N 0.000 description 4
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 4
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- NEHNMFOYXAPHSD-UHFFFAOYSA-N citronellal Chemical compound O=CCC(C)CCC=C(C)C NEHNMFOYXAPHSD-UHFFFAOYSA-N 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 4
- JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 4
- LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 description 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 3
- 229920004449 Halon® Polymers 0.000 description 3
- MEXUFEQDCXZEON-UHFFFAOYSA-N bromochlorodifluoromethane Chemical compound FC(F)(Cl)Br MEXUFEQDCXZEON-UHFFFAOYSA-N 0.000 description 3
- 239000000460 chlorine Substances 0.000 description 3
- 229910052801 chlorine Inorganic materials 0.000 description 3
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 description 2
- WTARULDDTDQWMU-RKDXNWHRSA-N (+)-β-pinene Chemical compound C1[C@H]2C(C)(C)[C@@H]1CCC2=C WTARULDDTDQWMU-RKDXNWHRSA-N 0.000 description 2
- WTARULDDTDQWMU-IUCAKERBSA-N (-)-Nopinene Natural products C1[C@@H]2C(C)(C)[C@H]1CCC2=C WTARULDDTDQWMU-IUCAKERBSA-N 0.000 description 2
- OYHQOLUKZRVURQ-NTGFUMLPSA-N (9Z,12Z)-9,10,12,13-tetratritiooctadeca-9,12-dienoic acid Chemical compound C(CCCCCCC\C(=C(/C\C(=C(/CCCCC)\[3H])\[3H])\[3H])\[3H])(=O)O OYHQOLUKZRVURQ-NTGFUMLPSA-N 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 2
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 2
- ZQTIKDIHRRLSRV-UHFFFAOYSA-N 1,1,1,2,2,3,3,4,4-nonafluorobutane Chemical compound FC(F)C(F)(F)C(F)(F)C(F)(F)F ZQTIKDIHRRLSRV-UHFFFAOYSA-N 0.000 description 2
- FYIRUPZTYPILDH-UHFFFAOYSA-N 1,1,1,2,3,3-hexafluoropropane Chemical compound FC(F)C(F)C(F)(F)F FYIRUPZTYPILDH-UHFFFAOYSA-N 0.000 description 2
- NSGXIBWMJZWTPY-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropane Chemical compound FC(F)(F)CC(F)(F)F NSGXIBWMJZWTPY-UHFFFAOYSA-N 0.000 description 2
- ZXVZGGVDYOBILI-UHFFFAOYSA-N 1,1,2,2,3,3-hexafluoropropane Chemical compound FC(F)C(F)(F)C(F)F ZXVZGGVDYOBILI-UHFFFAOYSA-N 0.000 description 2
- FPIPGXGPPPQFEQ-UHFFFAOYSA-N 13-cis retinol Natural products OCC=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-UHFFFAOYSA-N 0.000 description 2
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 2
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 2
- 241000723346 Cinnamomum camphora Species 0.000 description 2
- WTEVQBCEXWBHNA-UHFFFAOYSA-N Citral Natural products CC(C)=CCCC(C)=CC=O WTEVQBCEXWBHNA-UHFFFAOYSA-N 0.000 description 2
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 description 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 2
- 239000005642 Oleic acid Substances 0.000 description 2
- WTARULDDTDQWMU-UHFFFAOYSA-N Pseudopinene Natural products C1C2C(C)(C)C1CCC2=C WTARULDDTDQWMU-UHFFFAOYSA-N 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- UWHZIFQPPBDJPM-FPLPWBNLSA-M Vaccenic acid Natural products CCCCCC\C=C/CCCCCCCCCC([O-])=O UWHZIFQPPBDJPM-FPLPWBNLSA-M 0.000 description 2
- 235000021322 Vaccenic acid Nutrition 0.000 description 2
- FPIPGXGPPPQFEQ-BOOMUCAASA-N Vitamin A Natural products OC/C=C(/C)\C=C\C=C(\C)/C=C/C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-BOOMUCAASA-N 0.000 description 2
- OENHQHLEOONYIE-UKMVMLAPSA-N all-trans beta-carotene Natural products CC=1CCCC(C)(C)C=1/C=C/C(/C)=C/C=C/C(/C)=C/C=C/C=C(C)C=CC=C(C)C=CC1=C(C)CCCC1(C)C OENHQHLEOONYIE-UKMVMLAPSA-N 0.000 description 2
- FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 2
- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 2
- TUPZEYHYWIEDIH-WAIFQNFQSA-N beta-carotene Natural products CC(=C/C=C/C=C(C)/C=C/C=C(C)/C=C/C1=C(C)CCCC1(C)C)C=CC=C(/C)C=CC2=CCCCC2(C)C TUPZEYHYWIEDIH-WAIFQNFQSA-N 0.000 description 2
- 235000013734 beta-carotene Nutrition 0.000 description 2
- 239000011648 beta-carotene Substances 0.000 description 2
- 229930006722 beta-pinene Natural products 0.000 description 2
- 229960002747 betacarotene Drugs 0.000 description 2
- GZUXJHMPEANEGY-UHFFFAOYSA-N bromomethane Chemical compound BrC GZUXJHMPEANEGY-UHFFFAOYSA-N 0.000 description 2
- RJCQBQGAPKAMLL-UHFFFAOYSA-N bromotrifluoromethane Chemical compound FC(F)(F)Br RJCQBQGAPKAMLL-UHFFFAOYSA-N 0.000 description 2
- 229930008380 camphor Natural products 0.000 description 2
- 229960000846 camphor Drugs 0.000 description 2
- 229940043350 citral Drugs 0.000 description 2
- 235000000983 citronellal Nutrition 0.000 description 2
- 229930003633 citronellal Natural products 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- LCWMKIHBLJLORW-UHFFFAOYSA-N gamma-carene Natural products C1CC(=C)CC2C(C)(C)C21 LCWMKIHBLJLORW-UHFFFAOYSA-N 0.000 description 2
- WTEVQBCEXWBHNA-JXMROGBWSA-N geranial Chemical compound CC(C)=CCC\C(C)=C\C=O WTEVQBCEXWBHNA-JXMROGBWSA-N 0.000 description 2
- 150000008282 halocarbons Chemical class 0.000 description 2
- UKACHOXRXFQJFN-UHFFFAOYSA-N heptafluoropropane Chemical compound FC(F)C(F)(F)C(F)(F)F UKACHOXRXFQJFN-UHFFFAOYSA-N 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 2
- 235000001510 limonene Nutrition 0.000 description 2
- 229940087305 limonene Drugs 0.000 description 2
- 229940041616 menthol Drugs 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 231100000252 nontoxic Toxicity 0.000 description 2
- 230000003000 nontoxic effect Effects 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- SECPZKHBENQXJG-FPLPWBNLSA-N palmitoleic acid Chemical compound CCCCCC\C=C/CCCCCCCC(O)=O SECPZKHBENQXJG-FPLPWBNLSA-N 0.000 description 2
- GTLACDSXYULKMZ-UHFFFAOYSA-N pentafluoroethane Chemical compound FC(F)C(F)(F)F GTLACDSXYULKMZ-UHFFFAOYSA-N 0.000 description 2
- -1 polypropylene Polymers 0.000 description 2
- 235000011164 potassium chloride Nutrition 0.000 description 2
- 239000001103 potassium chloride Substances 0.000 description 2
- 239000002516 radical scavenger Substances 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- 239000011780 sodium chloride Substances 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- UWHZIFQPPBDJPM-BQYQJAHWSA-N trans-vaccenic acid Chemical compound CCCCCC\C=C\CCCCCCCCCC(O)=O UWHZIFQPPBDJPM-BQYQJAHWSA-N 0.000 description 2
- 235000019155 vitamin A Nutrition 0.000 description 2
- 239000011719 vitamin A Substances 0.000 description 2
- 229940045997 vitamin a Drugs 0.000 description 2
- GRWFGVWFFZKLTI-UHFFFAOYSA-N α-pinene Chemical compound CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 2
- OENHQHLEOONYIE-JLTXGRSLSA-N β-Carotene Chemical compound CC=1CCCC(C)(C)C=1\C=C\C(\C)=C\C=C\C(\C)=C\C=C\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C OENHQHLEOONYIE-JLTXGRSLSA-N 0.000 description 2
- CFSHSCBNZAKMAT-UHFFFAOYSA-N 1,1,1,2,3,4,4,4-octafluorobutane Chemical compound FC(F)(F)C(F)C(F)C(F)(F)F CFSHSCBNZAKMAT-UHFFFAOYSA-N 0.000 description 1
- GRWFGVWFFZKLTI-IUCAKERBSA-N 1S,5S-(-)-alpha-Pinene Natural products CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 1
- 241000566113 Branta sandvicensis Species 0.000 description 1
- 229910000975 Carbon steel Inorganic materials 0.000 description 1
- 241001522296 Erithacus rubecula Species 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-N Fluorane Chemical compound F KRHYYFGTRYWZRS-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 235000021319 Palmitoleic acid Nutrition 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000007853 buffer solution Substances 0.000 description 1
- 239000010962 carbon steel Substances 0.000 description 1
- 239000013043 chemical agent Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- SECPZKHBENQXJG-UHFFFAOYSA-N cis-palmitoleic acid Natural products CCCCCCC=CCCCCCCCC(O)=O SECPZKHBENQXJG-UHFFFAOYSA-N 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- KVBKAPANDHPRDG-UHFFFAOYSA-N dibromotetrafluoroethane Chemical compound FC(F)(Br)C(F)(F)Br KVBKAPANDHPRDG-UHFFFAOYSA-N 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 229940102396 methyl bromide Drugs 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 239000011120 plywood Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 235000002639 sodium chloride Nutrition 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 230000002110 toxicologic effect Effects 0.000 description 1
- 231100000027 toxicology Toxicity 0.000 description 1
- 238000010792 warming Methods 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62C—FIRE-FIGHTING
- A62C99/00—Subject matter not provided for in other groups of this subclass
- A62C99/0009—Methods of extinguishing or preventing the spread of fire by cooling down or suffocating the flames
- A62C99/0018—Methods of extinguishing or preventing the spread of fire by cooling down or suffocating the flames using gases or vapours that do not support combustion, e.g. steam, carbon dioxide
-
- A—HUMAN NECESSITIES
- A62—LIFE-SAVING; FIRE-FIGHTING
- A62D—CHEMICAL MEANS FOR EXTINGUISHING FIRES OR FOR COMBATING OR PROTECTING AGAINST HARMFUL CHEMICAL AGENTS; CHEMICAL MATERIALS FOR USE IN BREATHING APPARATUS
- A62D1/00—Fire-extinguishing compositions; Use of chemical substances in extinguishing fires
- A62D1/0028—Liquid extinguishing substances
- A62D1/0057—Polyhaloalkanes
Definitions
- the present invention relates to the field of fire extinguishing compositions and methods, and particularly to compositions and methods employing compositions comprised of hydrofluorocarbons and acid scavenging additives.
- bromine-containing compounds are effective fire fighting agents, those agents containing bromine or chlorine are asserted to be capable of the destruction of the earth's protective ozone layer.
- Halon 1301 has an Ozone Depletion Potential (ODP) rating of 10
- Halon 1211 has an ODP of 3.
- hydrofluorocarbons as extinguishing agents has been proposed only recently, for example as described in U.S. Patent 5,124,053 to Iikubo and Robin. Since the hydro luorocarbons do not contain bromine or chlorine, the compounds have no effect on the stratospheric ozone layer and their ODP is zero. It has been discovered that certain of these compounds, especially those with a higher ratio of hydrogen to fluorine in the molecule, can decompose to some extent in a fire, producing hydrogen fluoride, HF, which is potentially damaging to personnel and equipment if formed in large quantities.
- a method of extinguishing a fire that comprises introducing to the fire a fire extinguishing concentration of an extinguishant composition comprising, and preferably consisting essentially of, a hydrofluorocarbon and an acid-scavenging additive, and maintaining the concentration of the composition until the fire is extinguished.
- Fire extinguishing compositions comprising, or consisting essentially of, a hydrofluorocarbon and an acid-scavenging additive are also provided.
- a further object of the present invention is to provide fire extinguishing compositions comprising blends of hydrofluorocarbons and acid-scavenging additives, which blends are effective and safe in use.
- a further object of the present invention is to provide fire extinguishing compositions which produce reduced amounts of decomposition products compared to other fire extinguishing agents when employed in the extinguishment of fires.
- compositions comprising a hydrofluorocarbon in combination with an acid-scavenging additive provide particularly effective fire extingiiishants at concentrations safe for use. Because the compositions contain no bromine or chlorine, they have an ozone depletion potential of zero.
- compositions produce less decomposition products than the hydrofluorocarbon analogs, and hence are of reduced toxicity with regard to use in a fire scenario.
- the invention relates to methods for extinguishing fires which are improved by using these compositions as the fire extinguishing agents.
- extinguishant compositions may preferably consist essentially of the hydro luorocarbon and the acid-scavenger(s) .
- hydrofluorocarbons useful in accordance with the present invention include trifluoromethane (CF-H), pentafluoroethane (CF CF II) , 1, 1, 1,2-tetrafluoroethane (CF 3 CH 2 F) , 1,1, 1,2,3,3-hexafluoropropane (CF 3 CHFCF 2 H) , 1, 1,1,3,3,3-hexafluoropropane (CF CH CF ) , 1, 1,2,2,3,3-hexafluoropropane (HCF 2 CF 2 CF 2 H) , 1,1, 1,2, 3,3, 3-heptafluoropropane (CF 3 CHFCF_) , 1,1, 1, 2,2,3,3-heptafluoropropane (CF CF.CF H) , 1,1, 1,2,2,3,3,4,4-nonafluorobutane (CF 3 CF 2 CF 2 CF 2 II) , 1, 1,1,2,3,4,4, -octafluorobutane
- hydrofluorocarbons within the present invention are C 3 H 3 F 5 , C 4 I. 3 F 7 . 5 HF 3 F ⁇ , C ⁇ F ⁇ , C 5 H 3 F 9 , C 5 H 4 F B . and C ⁇ I ⁇ .
- Specific terpenes useful in accordance with the present invention include citral, citronellal, limonene, dipentene, menthol, alpha-pinene, beta-pinene, camphor, vitamin A beta-carotene, and isopro ⁇ enyl-1-methylcyclohexene.
- the terpenes preferably comprise from about 0.1% to about 10% by weight of the extinguishing composition.
- Specific unsaturated oils useful in accordance witli the present invention include oleic acid, linoleic acid, palinitoleic acid and vaccenic acid.
- the unsaturated oils preferably comprise from about 0.1% to about 10% by weight of the extinguishing composition.
- alkali metal halides useful in accordance with the present invention include sodium chloride, potassium chloride, sodium bromide and potassium bromide.
- the alkali metal halides preferably comprise from about 0.1% to about 10% by weight of the extinguishing composition.
- a method for extinguishing fires which includes the use of a composition comprised of a hydrofluorocarbon and an acid-scavenging additive as a fire ext nguishing agent.
- the compositions may be applied in the variety of methods employed for other halogenated hydrocarbons, including application in a flooding system, portable system or specialized system.
- the extinguishant is effective in low concentrations, and of course, at high concentrations as well.
- the concentration employed may depend to some extent on the nature of the fire, the combusting material and tiie circumstances of application.
- application rates preferably range from about 1% to about 25% v/v, and more preferably from about 2% and to about 15% v/v, of the hydrofluorocarbon component in the atmosphere.
- the acid-scavenging additives comprise from about 0.1% to about 10% by weight of the composition.
- the relative amounts of the hydrofluorocarbon and the acid-scavenging additive are not critical, but rather are dictated by the characteristics desired for the overall composition. For example, in certain applications there may be a greater need for low toxicity, and in other instances, the emphasis may be on cleanliness of the extinguishment .
- the methods for application of the described fire extinguishing compositions are those known to be useful for the Halon agents. In broad terms, these methods utilize application systems which typically include a supply of agent, a means for releasing or propelling the agent from its container, and one or more discharge nozzles to apply the agent into the hazard or directly onto the burning object.
- the agents of this invention may be used in total flooding systems in which the agent is introduced into an enclosed region surrounding a fire at a concentration sufficient to extinguish the fire.
- equipment or even rooms may be provided with a source of agent and appropriate piping, valves and controls so as to automatically and/or manually be introduced at appropriate concentrations in the event that fire should break out.
- the fire extinguishant may be pressurized with nitrogen or other inert gas at up to about 600 psig at ambient conditions.
- compositions of the invention may be applied to a fire through the use of conventional portable fire extinguishing equipment. It is usual to increase the pressure in portable fire extinguishers with nitrogen or other inert gases in order to ensure that the agent is completely expelled from the extinguisher. Systems in accordance witli this invention may be conveniently pressurized at any desirable pressure up to about 600 psig at ambient conditions.
- EXAMPLE 1 A test facility with a total internal volume of 1440 cubic feet was constructed from 2x4 lumber and 3/4" plywood. The enclosure was equipped with two 3 foot by 3 foot windows and two standard doors located on opposite walls. The delivery system consisted of a standard Halon cylinder connected to 1" carbon steel pipe via a stainless steel flexhose, terminating in a standard Halon nozzle located 6 inches down from the center of the ceiling.
- a large steel pan was filled with commercial n-heptane and placed in the center of the facility, and the n-heptane was then ignited. Thirty seconds after ignition, the doors to the enclosure were closed and the extinguishing agent released.
- the enclosure atmosphere was sampled after extinguishment of the fire by pulling a sample of the post-extinguishment atmosphere through a buffer solution contained in a polypropylene bubbler equipped with a 70 micron porous polyethylene frit. Fluoride and HF concentrations were determined employing a fluoride ion selective electrode (ISE).
- the post-extinguishment atmosphere was sampled at two locations, one at a height of 6 feet and the second at a height of 2 feet, both sampling points located 2 feet diagonally out from the corner of the enclosure.
- Example 2 The procedure of Example 1 was repeated employing G9 pounds of 1, 1, 1,2, 3,3 ,3-heptafluoropropane (CF CHFCF ) to which had been added 1.0 pounds of dipeutene (1.4 % by weight) . Analysis showed the concentration of HF to be 2403 ppm at the 6 foot location and 1202 ppm at the 2 foot location.
- CF CHFCF 1, 1, 1,2, 3,3 ,3-heptafluoropropane
- This example demonstrates the advantageous effect of the addition of a small amount of an acid-scavenging additive to the hydrofluorocarbon.
- the amount of HF produced was reduced by 32% at the 6 foot location and by 38% at the 2 foot location.
- Example 3 The procedure of Example 1 was repeated employing a small steel pan filled with n-heptane. Analysis of the post-extinguishment atmosphere showed a concentration of HF of 50 ppm at the 6 foot location and 11 ppm at the 2 foot location.
- EXAMPLE 4 The procedure of Example 3 was repeated employing 69 pounds of 1, 1,1,2,3,3,3-heptafluoropropane (CF-CHFCF..,) to which had been added 1.0 pounds of limonene (1.4 % by weight) . Following extinguishment of the fire, analysis showed the concentration of HF to be 32 ppm at the 6 foot location and 7 ppm at the 2 foot location.
- CF-CHFCF.. 1, 1,1,2,3,3,3-heptafluoropropane
- This example demonstrates the advantageous effect of the addition of a small amount of an acid-scavenging additive to the hydrofluorocarbon.
- the amount of HF produced was reduced by 36% at botli locations.
- Desirable results are achieved for combinations of 90% to 99.9% by weight of the 1, 1, 1 , 2,3,3 , 3-heptafluoropropane and of 0.1% to 10.0% of the acid-scavenger.
- suitable results are obtained for fire extinguishant compositions comprising blends of the foregoing ac d-scavengers and the various other hydrofluorocarbons defined herein, including for example, trifluoromethane, pentafluoroethane, 1,1,1, 2-tetrafluoroethane, 1,1,1,2,3,3-hexafluoropropane, 1,1,1,3,3,3-hexafluoropropane, 1,1,2,2,3, 3-hexafluoropropane, 1,1,1,2,2,3 ,3-heptafluoropropane, 1,1,1,2,2,3,3,4,4-nonafluorobutane, 1,1,1,2,3,4,4,4-octafluorobutane and 1, 1, 1, 1,3,3,
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Abstract
Procédés utilisés pour éteindre un incendie avec des compositions comprenant un hydrofluorocarbone et un additif adsorbant l'acide. Ces compositions d'extinction des incendies contiennent de préférence un ou plusieurs hydrocarbures de formule CxHyFz, dans laquelle (y + z) = (2x + 2), y étant inférieur ou égal à x. L'additif adsorbant l'acide est de préférence sélectionné dans le groupe formé par les terpènes, les huiles non saturées, le bicarbonate de sodium, le bicarbonate de potassium, le phosphate de mono-ammonium, les halogénures de métaux alcalins et l'urée.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US21834794A | 1994-03-28 | 1994-03-28 | |
| PCT/US1995/003490 WO1995026218A1 (fr) | 1994-03-28 | 1995-03-21 | Procedes et compositions d'extinction des incendies sans danger pour la couche d'ozone |
| US218347 | 1998-12-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP0752900A1 true EP0752900A1 (fr) | 1997-01-15 |
Family
ID=22814744
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP95913781A Withdrawn EP0752900A1 (fr) | 1994-03-28 | 1995-03-21 | Procedes et compositions d'extinction des incendies sans danger pour la couche d'ozone |
Country Status (13)
| Country | Link |
|---|---|
| EP (1) | EP0752900A1 (fr) |
| JP (1) | JPH09510891A (fr) |
| KR (1) | KR970702089A (fr) |
| AU (1) | AU2103995A (fr) |
| CA (1) | CA2185910A1 (fr) |
| HU (1) | HU9602662D0 (fr) |
| IL (1) | IL113086A0 (fr) |
| MX (1) | MX9604320A (fr) |
| NO (1) | NO964046L (fr) |
| NZ (1) | NZ283089A (fr) |
| PL (1) | PL316629A1 (fr) |
| WO (1) | WO1995026218A1 (fr) |
| ZA (1) | ZA952385B (fr) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1283203B1 (it) * | 1996-03-07 | 1998-04-16 | Ausimont Spa | Composizioni estinguenti la fiamma |
| IT1282378B1 (it) * | 1996-04-24 | 1998-03-20 | Ausimont Spa | Perfluoroelastomeri a base di diossoli |
| ITMI981506A1 (it) | 1998-06-30 | 1999-12-30 | Ausimont Spa | Manufatti di fluoropolimeri amorfi |
| ITMI981505A1 (it) * | 1998-06-30 | 1999-12-30 | Ausimont Spa | Purificazione di polimeri fluorurati |
| IT1312320B1 (it) | 1999-05-25 | 2002-04-15 | Ausimont Spa | Membrane di polimeri amorfi (per) fluorurati. |
| US7405334B2 (en) | 2003-05-23 | 2008-07-29 | E. I. Du Pont De Nemours And Company | Process for the reduction of acidic contaminates in fluorinated hydrocarbons |
| US20060016608A1 (en) * | 2004-07-21 | 2006-01-26 | Kidde Ip Holdings Limited | Discharge of fire extinguishing agent |
| IT1391013B1 (it) * | 2008-07-01 | 2011-10-27 | Explosafe Int B V | Agenti estinguenti a base di miscele di fluoroiodo-carburi additivati con composti detossificanti. |
| US9308406B2 (en) | 2011-10-25 | 2016-04-12 | Kidde Technologies, Inc. | Automatic fire extinguishing system having outlet dimensions sized relative to propellant gas pressure |
| US9192798B2 (en) | 2011-10-25 | 2015-11-24 | Kidde Technologies, Inc. | Automatic fire extinguishing system with gaseous and dry powder fire suppression agents |
| US9302128B2 (en) | 2011-10-25 | 2016-04-05 | Kidde Technologies, Inc. | Automatic fire extinguishing system with internal dip tube |
| US9463341B2 (en) | 2011-10-25 | 2016-10-11 | Kidde Technologies, Inc. | N2/CO2 fire extinguishing system propellant gas mixture |
| US9168406B2 (en) | 2012-03-15 | 2015-10-27 | Kidde Technologies, Inc. | Automatic actuation of a general purpose hand extinguisher |
| WO2016195635A1 (fr) * | 2015-05-29 | 2016-12-08 | Sevo Systems, Inc. | Procédé de distribution d'une composition d'extinction à un incendie |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE789667A (fr) * | 1971-10-08 | 1973-04-04 | Rhone Progil | Composition extinctrice liquide a base d'hydrocarbures halogenes |
| GB8600853D0 (en) * | 1986-01-15 | 1986-02-19 | Thacker D A | Fire extinguishant formulation |
| US4954271A (en) * | 1988-10-06 | 1990-09-04 | Tag Investments, Inc. | Non-toxic fire extinguishant |
| US5124053A (en) * | 1989-08-21 | 1992-06-23 | Great Lakes Chemical Corporation | Fire extinguishing methods and blends utilizing hydrofluorocarbons |
| US5141654A (en) * | 1989-11-14 | 1992-08-25 | E. I. Du Pont De Nemours And Company | Fire extinguishing composition and process |
| US5084190A (en) * | 1989-11-14 | 1992-01-28 | E. I. Du Pont De Nemours And Company | Fire extinguishing composition and process |
-
1995
- 1995-03-21 NZ NZ283089A patent/NZ283089A/en unknown
- 1995-03-21 HU HU9602662A patent/HU9602662D0/hu unknown
- 1995-03-21 WO PCT/US1995/003490 patent/WO1995026218A1/fr not_active Ceased
- 1995-03-21 CA CA002185910A patent/CA2185910A1/fr not_active Abandoned
- 1995-03-21 EP EP95913781A patent/EP0752900A1/fr not_active Withdrawn
- 1995-03-21 PL PL95316629A patent/PL316629A1/xx unknown
- 1995-03-21 MX MX9604320A patent/MX9604320A/es unknown
- 1995-03-21 JP JP7525205A patent/JPH09510891A/ja active Pending
- 1995-03-21 AU AU21039/95A patent/AU2103995A/en not_active Abandoned
- 1995-03-22 IL IL11308695A patent/IL113086A0/xx unknown
- 1995-03-23 ZA ZA952385A patent/ZA952385B/xx unknown
-
1996
- 1996-09-25 KR KR1019960705361A patent/KR970702089A/ko not_active Withdrawn
- 1996-09-26 NO NO964046A patent/NO964046L/no unknown
Non-Patent Citations (1)
| Title |
|---|
| See references of WO9526218A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| AU2103995A (en) | 1995-10-17 |
| NZ283089A (en) | 1997-07-27 |
| NO964046D0 (no) | 1996-09-26 |
| JPH09510891A (ja) | 1997-11-04 |
| PL316629A1 (en) | 1997-02-03 |
| NO964046L (no) | 1996-09-26 |
| IL113086A0 (en) | 1995-06-29 |
| HU9602662D0 (en) | 1996-11-28 |
| CA2185910A1 (fr) | 1995-10-05 |
| ZA952385B (en) | 1995-12-14 |
| KR970702089A (ko) | 1997-05-13 |
| WO1995026218A1 (fr) | 1995-10-05 |
| MX9604320A (es) | 1997-06-28 |
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