CA2095640C - Composition servant a eteindre un incendie et methode de production de cette composition - Google Patents

Composition servant a eteindre un incendie et methode de production de cette composition Download PDF

Info

Publication number: CA2095640C
Authority: CA; Canada
Prior art keywords: chloro; pentafluoropropane; hexafluoropropane; dichloro; chf2
Prior art date: 1990-11-15
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 - Lifetime

Application number

CA002095640A

Other languages

English (en)

Other versions

CA2095640A1 (fr

Inventor

Richard Edward Fernandez

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

EIDP Inc

Original Assignee

EI Du Pont de Nemours and Co

Priority date (The priority date 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 date listed.)

1990-11-15

Filing date

1990-11-15

Publication date

2004-10-19

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=32961126&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CA2095640(C) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1990-11-15 Application filed by EI Du Pont de Nemours and Co filed Critical EI Du Pont de Nemours and Co

1992-05-16 Publication of CA2095640A1 publication Critical patent/CA2095640A1/fr

2004-10-19 Application granted granted Critical

2004-10-19 Publication of CA2095640C publication Critical patent/CA2095640C/fr

2010-11-15 Anticipated expiration legal-status Critical

Status Expired - Lifetime legal-status Critical Current

Links

238000000034 method Methods 0.000 title claims abstract description 29
239000000203 mixture Substances 0.000 title abstract description 18
239000000463 material Substances 0.000 claims description 20
238000002485 combustion reaction Methods 0.000 claims description 15
150000008282 halocarbons Chemical class 0.000 claims description 14
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 11
239000001301 oxygen Substances 0.000 claims description 11
229910052760 oxygen Inorganic materials 0.000 claims description 11
BOUGCJDAQLKBQH-UHFFFAOYSA-N 1-chloro-1,2,2,2-tetrafluoroethane Chemical compound FC(Cl)C(F)(F)F BOUGCJDAQLKBQH-UHFFFAOYSA-N 0.000 claims description 10
GTLACDSXYULKMZ-UHFFFAOYSA-N pentafluoroethane Chemical compound FC(F)C(F)(F)F GTLACDSXYULKMZ-UHFFFAOYSA-N 0.000 claims description 10
OHMHBGPWCHTMQE-UHFFFAOYSA-N 2,2-dichloro-1,1,1-trifluoroethane Chemical compound FC(F)(F)C(Cl)Cl OHMHBGPWCHTMQE-UHFFFAOYSA-N 0.000 claims description 8
LVGUZGTVOIAKKC-UHFFFAOYSA-N 1,1,1,2-tetrafluoroethane Chemical compound FCC(F)(F)F LVGUZGTVOIAKKC-UHFFFAOYSA-N 0.000 claims description 7
RWRIWBAIICGTTQ-UHFFFAOYSA-N difluoromethane Chemical compound FCF RWRIWBAIICGTTQ-UHFFFAOYSA-N 0.000 claims description 6
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 claims description 4
NSGXIBWMJZWTPY-UHFFFAOYSA-N 1,1,1,3,3,3-hexafluoropropane Chemical compound FC(F)(F)CC(F)(F)F NSGXIBWMJZWTPY-UHFFFAOYSA-N 0.000 claims description 4
WXGNWUVNYMJENI-UHFFFAOYSA-N 1,1,2,2-tetrafluoroethane Chemical compound FC(F)C(F)F WXGNWUVNYMJENI-UHFFFAOYSA-N 0.000 claims description 4
YMRMDGSNYHCUCL-UHFFFAOYSA-N 1,2-dichloro-1,1,2-trifluoroethane Chemical compound FC(Cl)C(F)(F)Cl YMRMDGSNYHCUCL-UHFFFAOYSA-N 0.000 claims description 4
XAHBEACGJQDUPF-UHFFFAOYSA-N 1,2-dichloro-1,1,3,3,3-pentafluoropropane Chemical compound FC(F)(F)C(Cl)C(F)(F)Cl XAHBEACGJQDUPF-UHFFFAOYSA-N 0.000 claims description 4
IDSKMUOSMAUASS-UHFFFAOYSA-N 1,2-dichloro-1,2-difluoroethane Chemical compound FC(Cl)C(F)Cl IDSKMUOSMAUASS-UHFFFAOYSA-N 0.000 claims description 4
UHMWWIKRVZTBBR-UHFFFAOYSA-N 1-chloro-1,1,2,2,3-pentafluoropropane Chemical compound FCC(F)(F)C(F)(F)Cl UHMWWIKRVZTBBR-UHFFFAOYSA-N 0.000 claims description 4
JQZFYIGAYWLRCC-UHFFFAOYSA-N 1-chloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)C(F)(F)Cl JQZFYIGAYWLRCC-UHFFFAOYSA-N 0.000 claims description 4
JODPGPKOJGDHSV-UHFFFAOYSA-N 1-chloro-1,1,2,3,3,3-hexafluoropropane Chemical compound FC(F)(F)C(F)C(F)(F)Cl JODPGPKOJGDHSV-UHFFFAOYSA-N 0.000 claims description 4
FXSNEEBOGAOVIM-UHFFFAOYSA-N 1-chloro-1,2,2,3,3-pentafluoropropane Chemical compound FC(F)C(F)(F)C(F)Cl FXSNEEBOGAOVIM-UHFFFAOYSA-N 0.000 claims description 4
JEWUXLHWYRSHJK-UHFFFAOYSA-N 2,2-dichloro-1,1,1,3,3-pentafluoropropane Chemical compound FC(F)C(Cl)(Cl)C(F)(F)F JEWUXLHWYRSHJK-UHFFFAOYSA-N 0.000 claims description 4
SCDLWHGUKGDYQD-UHFFFAOYSA-N 2-chloro-1,1,1,2,3,3-hexafluoropropane Chemical compound FC(F)C(F)(Cl)C(F)(F)F SCDLWHGUKGDYQD-UHFFFAOYSA-N 0.000 claims description 4
COAUHYBSXMIJDK-UHFFFAOYSA-N 3,3-dichloro-1,1,1,2,2-pentafluoropropane Chemical compound FC(F)(F)C(F)(F)C(Cl)Cl COAUHYBSXMIJDK-UHFFFAOYSA-N 0.000 claims description 4
PUFSJRPTJJPPJP-UHFFFAOYSA-N 3-chloro-1,1,1,2,2,3-hexafluoropropane Chemical compound FC(Cl)C(F)(F)C(F)(F)F PUFSJRPTJJPPJP-UHFFFAOYSA-N 0.000 claims description 4
VOPWNXZWBYDODV-UHFFFAOYSA-N Chlorodifluoromethane Chemical compound FC(F)Cl VOPWNXZWBYDODV-UHFFFAOYSA-N 0.000 claims description 4
SUAMPXQALWYDBK-UHFFFAOYSA-N 1,1,1,2,2,3-hexafluoropropane Chemical compound FCC(F)(F)C(F)(F)F SUAMPXQALWYDBK-UHFFFAOYSA-N 0.000 claims description 3
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 claims description 3
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 claims description 3
UJIGKESMIPTWJH-UHFFFAOYSA-N 1,3-dichloro-1,1,2,2,3-pentafluoropropane Chemical compound FC(Cl)C(F)(F)C(F)(F)Cl UJIGKESMIPTWJH-UHFFFAOYSA-N 0.000 claims description 3
LLJWABOOFANACB-UHFFFAOYSA-N 1-chloro-1,1,3,3,3-pentafluoropropane Chemical compound FC(F)(F)CC(F)(F)Cl LLJWABOOFANACB-UHFFFAOYSA-N 0.000 claims description 3
BKWAVXQSZLEURV-UHFFFAOYSA-N 2-chloro-1,1,1,3,3,3-hexafluoropropane Chemical compound FC(F)(F)C(Cl)C(F)(F)F BKWAVXQSZLEURV-UHFFFAOYSA-N 0.000 claims description 3
XTRPJEPJFXGYCI-UHFFFAOYSA-N 3-chloro-1,1,1,2,2-pentafluoropropane Chemical compound FC(F)(F)C(F)(F)CCl XTRPJEPJFXGYCI-UHFFFAOYSA-N 0.000 claims description 3
UKACHOXRXFQJFN-UHFFFAOYSA-N heptafluoropropane Chemical compound FC(F)C(F)(F)C(F)(F)F UKACHOXRXFQJFN-UHFFFAOYSA-N 0.000 claims description 3
OIQOUHIUUREZOM-UHFFFAOYSA-N 1,1-dichloro-1,2-difluoroethane Chemical compound FCC(F)(Cl)Cl OIQOUHIUUREZOM-UHFFFAOYSA-N 0.000 claims description 2
AYAIRPGAABBRLY-UHFFFAOYSA-N 1-chloro-1,1,2,2,3,3-hexafluoropropane Chemical compound FC(F)C(F)(F)C(F)(F)Cl AYAIRPGAABBRLY-UHFFFAOYSA-N 0.000 claims description 2
CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 abstract description 21
230000000694 effects Effects 0.000 abstract description 15
-1 fluoro-substituted ethane Chemical group 0.000 abstract description 8
238000010792 warming Methods 0.000 abstract description 6
239000005437 stratosphere Substances 0.000 abstract description 4
OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 abstract description 2
239000003795 chemical substances by application Substances 0.000 description 23
UHCBBWUQDAVSMS-UHFFFAOYSA-N fluoroethane Chemical class CCF UHCBBWUQDAVSMS-UHFFFAOYSA-N 0.000 description 15
239000007789 gas Substances 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 7
229910052794 bromium Inorganic materials 0.000 description 7
238000009835 boiling Methods 0.000 description 6
230000000747 cardiac effect Effects 0.000 description 6
239000000446 fuel Substances 0.000 description 6
MEXUFEQDCXZEON-UHFFFAOYSA-N bromochlorodifluoromethane Chemical compound FC(F)(Cl)Br MEXUFEQDCXZEON-UHFFFAOYSA-N 0.000 description 5
229910052801 chlorine Inorganic materials 0.000 description 5
TXEYQDLBPFQVAA-UHFFFAOYSA-N tetrafluoromethane Chemical compound FC(F)(F)F TXEYQDLBPFQVAA-UHFFFAOYSA-N 0.000 description 5
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 4
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
125000001246 bromo group Chemical group Br* 0.000 description 4
239000000460 chlorine Substances 0.000 description 4
239000000123 paper Substances 0.000 description 4
150000003254 radicals Chemical class 0.000 description 4
230000035945 sensitivity Effects 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
UCTWMZQNUQWSLP-VIFPVBQESA-N (R)-adrenaline Chemical compound CNC[C@H](O)C1=CC=C(O)C(O)=C1 UCTWMZQNUQWSLP-VIFPVBQESA-N 0.000 description 3
241000282472 Canis lupus familiaris Species 0.000 description 3
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
RJCQBQGAPKAMLL-UHFFFAOYSA-N bromotrifluoromethane Chemical compound FC(F)(F)Br RJCQBQGAPKAMLL-UHFFFAOYSA-N 0.000 description 3
150000001875 compounds Chemical class 0.000 description 3
230000007613 environmental effect Effects 0.000 description 3
WMIYKQLTONQJES-UHFFFAOYSA-N hexafluoroethane Chemical compound FC(F)(F)C(F)(F)F WMIYKQLTONQJES-UHFFFAOYSA-N 0.000 description 3
239000007788 liquid Substances 0.000 description 3
239000003380 propellant Substances 0.000 description 3
239000002023 wood Substances 0.000 description 3
229930182837 (R)-adrenaline Natural products 0.000 description 2
RFCAUADVODFSLZ-UHFFFAOYSA-N 1-Chloro-1,1,2,2,2-pentafluoroethane Chemical compound FC(F)(F)C(F)(F)Cl RFCAUADVODFSLZ-UHFFFAOYSA-N 0.000 description 2
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
239000004340 Chloropentafluoroethane Substances 0.000 description 2
238000010521 absorption reaction Methods 0.000 description 2
UCTWMZQNUQWSLP-UHFFFAOYSA-N adrenaline Chemical compound CNCC(O)C1=CC=C(O)C(O)=C1 UCTWMZQNUQWSLP-UHFFFAOYSA-N 0.000 description 2
206010003119 arrhythmia Diseases 0.000 description 2
239000011324 bead Substances 0.000 description 2
235000019406 chloropentafluoroethane Nutrition 0.000 description 2
125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 2
229960005139 epinephrine Drugs 0.000 description 2
239000004744 fabric Substances 0.000 description 2
239000011521 glass Substances 0.000 description 2
239000004033 plastic Substances 0.000 description 2
229920003023 plastic Polymers 0.000 description 2
230000005855 radiation Effects 0.000 description 2
239000003507 refrigerant Substances 0.000 description 2
230000002459 sustained effect Effects 0.000 description 2
238000012360 testing method Methods 0.000 description 2
231100000419 toxicity Toxicity 0.000 description 2
230000001988 toxicity Effects 0.000 description 2
239000005436 troposphere Substances 0.000 description 2
206010002091 Anaesthesia Diseases 0.000 description 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
239000004604 Blowing Agent Substances 0.000 description 1
229920004449 Halon® Polymers 0.000 description 1
206010070834 Sensitisation Diseases 0.000 description 1
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 1
208000017379 Undifferentiated connective tissue syndrome Diseases 0.000 description 1
238000009825 accumulation Methods 0.000 description 1
230000002411 adverse Effects 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
230000037005 anaesthesia Effects 0.000 description 1
230000036592 analgesia Effects 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
NEHMKBQYUWJMIP-UHFFFAOYSA-N chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 1
PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
229910001882 dioxygen Inorganic materials 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
229960003072 epinephrine hydrochloride Drugs 0.000 description 1
239000006260 foam Substances 0.000 description 1
239000005337 ground glass Substances 0.000 description 1
230000007774 longterm Effects 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
238000005259 measurement Methods 0.000 description 1
MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 description 1
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical class C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
238000013508 migration Methods 0.000 description 1
230000005012 migration Effects 0.000 description 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
QYSGYZVSCZSLHT-UHFFFAOYSA-N octafluoropropane Chemical compound FC(F)(F)C(F)(F)C(F)(F)F QYSGYZVSCZSLHT-UHFFFAOYSA-N 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
229960004065 perflutren Drugs 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
230000002265 prevention Effects 0.000 description 1
230000003449 preventive effect Effects 0.000 description 1
238000005086 pumping Methods 0.000 description 1
238000011160 research Methods 0.000 description 1
230000008313 sensitization Effects 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
238000012546 transfer Methods 0.000 description 1

Classifications

- 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

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Business, Economics & Management (AREA)
Emergency Management (AREA)
Fire-Extinguishing Compositions (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CA002095640A 1990-11-15 1990-11-15 Composition servant a eteindre un incendie et methode de production de cette composition Expired - Lifetime CA2095640C (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
PCT/US1990/006692 WO1992008520A1 (fr)	1990-11-15	1990-11-15	Procede et composition pour l'extinction d'incendies

Publications (2)

Publication Number	Publication Date
CA2095640A1 CA2095640A1 (fr)	1992-05-16
CA2095640C true CA2095640C (fr)	2004-10-19

Family

ID=32961126

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA002095640A Expired - Lifetime CA2095640C (fr)	1990-11-15	1990-11-15	Composition servant a eteindre un incendie et methode de production de cette composition

Country Status (6)

Country	Link
EP (1)	EP0557275B1 (fr)
JP (1)	JP3558630B2 (fr)
CA (1)	CA2095640C (fr)
DE (1)	DE69028119T2 (fr)
ES (1)	ES2090301T3 (fr)
WO (1)	WO1992008520A1 (fr)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5040609A (en) *	1989-10-04	1991-08-20	E. I. Du Pont De Nemours And Company	Fire extinguishing composition and process
AU2002951075A0 (en) *	2002-08-29	2002-09-12	Commonwealth Scientific And Industrial Research Organisation	Twin roll casting of magnesium and magnesium alloys
US8444873B2 (en)	2009-06-12	2013-05-21	Solvay Fluor Gmbh	Refrigerant composition
ES2685512T3 (es)	2011-11-18	2018-10-09	Minimax Gmbh & Co. Kg	Instalación para la extinción o inertización con un agente de extinción sintético líquido

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US1926395A (en) *	1930-07-31	1933-09-12	Frigidaire Corp	Process of preventing fire by nontoxic substances
GB1132636A (en) *	1965-09-22	1968-11-06	Montedison Spa	Improvements in or relating to flame-extinguishing compositions
NL7006794A (fr) *	1969-05-16	1970-11-18
US3844354A (en) *	1973-07-11	1974-10-29	Dow Chemical Co	Halogenated fire extinguishing agent for total flooding system
US4459213A (en) *	1982-12-30	1984-07-10	Secom Co., Ltd.	Fire-extinguisher composition
US4954271A (en) *	1988-10-06	1990-09-04	Tag Investments, Inc.	Non-toxic fire extinguishant

1990
- 1990-11-15 EP EP91901121A patent/EP0557275B1/fr not_active Revoked
- 1990-11-15 WO PCT/US1990/006692 patent/WO1992008520A1/fr not_active Ceased
- 1990-11-15 ES ES91901121T patent/ES2090301T3/es not_active Expired - Lifetime
- 1990-11-15 JP JP50148091A patent/JP3558630B2/ja not_active Expired - Fee Related
- 1990-11-15 CA CA002095640A patent/CA2095640C/fr not_active Expired - Lifetime
- 1990-11-15 DE DE69028119T patent/DE69028119T2/de not_active Revoked

Also Published As

Publication number	Publication date
JPH06501628A (ja)	1994-02-24
DE69028119D1 (de)	1996-09-19
ES2090301T3 (es)	1996-10-16
EP0557275A1 (fr)	1993-09-01
DE69028119T2 (de)	1997-02-20
JP3558630B2 (ja)	2004-08-25
EP0557275A4 (en)	1993-09-29
CA2095640A1 (fr)	1992-05-16
EP0557275B1 (fr)	1996-08-14
WO1992008520A1 (fr)	1992-05-29

Legal Events

Date	Code	Title	Description
1997-10-07	EEER	Examination request
2010-11-15	MKLA	Lapsed
2012-12-02	MKEC	Expiry (correction)	Effective date: 20121202

Publication	Publication Date	Title
US5141654A (en)	1992-08-25	Fire extinguishing composition and process
US5084190A (en)	1992-01-28	Fire extinguishing composition and process
US5040609A (en)	1991-08-20	Fire extinguishing composition and process
US5115868A (en)	1992-05-26	Fire extinguishing composition and process
EP0930918A2 (fr)	1999-07-28	Melanges d'hydrobromocarbures destines a la protection contre les incendies et les explosions
CA2027273A1 (fr)	1991-04-11	Compositions, procedes et systemes d'extinction mettant en oeuvre du bromodifluoromethane
CA2036563A1 (fr)	1991-09-03	Methode d'extinction des feux et compositions utilisant le 2-chloro-1,1,1,2-tetrafluoroethane
JP2580075B2 (ja)	1997-02-12	ヒドロフルオロカーボンを用いる消火方法及び消火用ブレンド
CA2095640C (fr)	2004-10-19	Composition servant a eteindre un incendie et methode de production de cette composition
JP3558631B2 (ja)	2004-08-25	防火方法および防火組成物
CA2449614C (fr)	2004-12-28	Agent extincteur; procede de fabrication
JPH06501629A (ja)	1994-02-24	消火組成物及び方法