IL32098A - Fire-fighting foam - Google Patents

Fire-fighting foam

Info

Publication number: IL32098A
Authority: IL; Israel
Prior art keywords: agent; group; derived; composition; foam
Prior art date: 1968-04-29

Application number

IL32098A

Other languages

English (en)

Other versions

IL32098A0 (en

Original Assignee

Ici Ltd

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.)

1968-04-29

Filing date

1969-04-29

Publication date

1972-07-26

1968-04-29 Priority claimed from GB5078768A external-priority patent/GB1270661A/en

1969-04-29 Application filed by Ici Ltd filed Critical Ici Ltd

1969-06-25 Publication of IL32098A0 publication Critical patent/IL32098A0/xx

1972-07-26 Publication of IL32098A publication Critical patent/IL32098A/en

Links

239000006260 foam Substances 0.000 title claims description 95
238000000034 method Methods 0.000 claims description 49
239000003795 chemical substances by application Substances 0.000 claims description 46
239000000203 mixture Substances 0.000 claims description 44
150000001875 compounds Chemical class 0.000 claims description 28
BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims description 22
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 15
-1 polyethylene Polymers 0.000 claims description 15
239000011734 sodium Substances 0.000 claims description 13
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 11
238000005187 foaming Methods 0.000 claims description 11
229910052708 sodium Inorganic materials 0.000 claims description 11
239000002253 acid Substances 0.000 claims description 10
125000000217 alkyl group Chemical group 0.000 claims description 10
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 9
150000001450 anions Chemical class 0.000 claims description 9
150000003839 salts Chemical group 0.000 claims description 8
QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 7
229910052739 hydrogen Inorganic materials 0.000 claims description 7
239000001257 hydrogen Substances 0.000 claims description 7
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
229910052783 alkali metal Inorganic materials 0.000 claims description 6
125000004429 atom Chemical group 0.000 claims description 6
150000001732 carboxylic acid derivatives Chemical group 0.000 claims description 6
150000004985 diamines Chemical class 0.000 claims description 6
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 5
150000001340 alkali metals Chemical class 0.000 claims description 5
229910052700 potassium Inorganic materials 0.000 claims description 5
239000011591 potassium Substances 0.000 claims description 5
229920002153 Hydroxypropyl cellulose Polymers 0.000 claims description 4
229910052799 carbon Inorganic materials 0.000 claims description 4
239000001863 hydroxypropyl cellulose Substances 0.000 claims description 4
235000010977 hydroxypropyl cellulose Nutrition 0.000 claims description 4
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical group OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 claims description 4
125000005207 tetraalkylammonium group Chemical group 0.000 claims description 4
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
150000001721 carbon Chemical group 0.000 claims description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 4
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 4
229910052794 bromium Inorganic materials 0.000 claims 4
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
239000005977 Ethylene Substances 0.000 claims 1
239000004698 Polyethylene Substances 0.000 claims 1
229910052740 iodine Inorganic materials 0.000 claims 1
239000011630 iodine Substances 0.000 claims 1
229920000573 polyethylene Polymers 0.000 claims 1
125000004436 sodium atom Chemical group 0.000 claims 1
229940124530 sulfonamide Drugs 0.000 claims 1
125000000565 sulfonamide group Chemical group 0.000 claims 1
239000004094 surface-active agent Substances 0.000 description 51
238000006243 chemical reaction Methods 0.000 description 21
102000004169 proteins and genes Human genes 0.000 description 20
108090000623 proteins and genes Proteins 0.000 description 20
239000000843 powder Substances 0.000 description 14
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 13
239000000446 fuel Substances 0.000 description 12
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 10
239000000243 solution Substances 0.000 description 9
239000007864 aqueous solution Substances 0.000 description 8
NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical group FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 description 7
239000000126 substance Substances 0.000 description 7
239000013256 coordination polymer Substances 0.000 description 6
239000004088 foaming agent Substances 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
239000000463 material Substances 0.000 description 5
239000004215 Carbon black (E152) Substances 0.000 description 4
UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
150000007513 acids Chemical class 0.000 description 4
125000003277 amino group Chemical group 0.000 description 4
125000000129 anionic group Chemical group 0.000 description 4
239000002585 base Substances 0.000 description 4
229910052731 fluorine Inorganic materials 0.000 description 4
229930195733 hydrocarbon Natural products 0.000 description 4
150000002430 hydrocarbons Chemical class 0.000 description 4
239000007788 liquid Substances 0.000 description 4
229920001296 polysiloxane Polymers 0.000 description 4
235000017557 sodium bicarbonate Nutrition 0.000 description 4
229910000831 Steel Inorganic materials 0.000 description 3
239000003513 alkali Substances 0.000 description 3
239000006265 aqueous foam Substances 0.000 description 3
125000004432 carbon atom Chemical group C* 0.000 description 3
125000002091 cationic group Chemical group 0.000 description 3
230000006378 damage Effects 0.000 description 3
125000001153 fluoro group Chemical group F* 0.000 description 3
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 3
238000005192 partition Methods 0.000 description 3
125000005010 perfluoroalkyl group Chemical group 0.000 description 3
235000015497 potassium bicarbonate Nutrition 0.000 description 3
TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical class [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 3
239000012460 protein solution Substances 0.000 description 3
238000007789 sealing Methods 0.000 description 3
239000010959 steel Substances 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 2
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 2
WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 2
150000001408 amides Chemical class 0.000 description 2
150000001412 amines Chemical class 0.000 description 2
JPNZKPRONVOMLL-UHFFFAOYSA-N azane;octadecanoic acid Chemical class [NH4+].CCCCCCCCCCCCCCCCCC([O-])=O JPNZKPRONVOMLL-UHFFFAOYSA-N 0.000 description 2
150000003841 chloride salts Chemical class 0.000 description 2
239000000470 constituent Substances 0.000 description 2
238000010790 dilution Methods 0.000 description 2
239000012895 dilution Substances 0.000 description 2
230000000694 effects Effects 0.000 description 2
238000011156 evaluation Methods 0.000 description 2
239000011737 fluorine Substances 0.000 description 2
239000003292 glue Substances 0.000 description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
229910052744 lithium Inorganic materials 0.000 description 2
102000035118 modified proteins Human genes 0.000 description 2
108091005573 modified proteins Proteins 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 2
239000007787 solid Substances 0.000 description 2
229910021653 sulphate ion Inorganic materials 0.000 description 2
NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical compound CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
102000009027 Albumins Human genes 0.000 description 1
108010088751 Albumins Proteins 0.000 description 1
239000004254 Ammonium phosphate Substances 0.000 description 1
229910001369 Brass Inorganic materials 0.000 description 1
229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
239000001692 EU approved anti-caking agent Substances 0.000 description 1
102000006395 Globulins Human genes 0.000 description 1
108010044091 Globulins Proteins 0.000 description 1
244000068988 Glycine max Species 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
239000005905 Hydrolysed protein Substances 0.000 description 1
102000011782 Keratins Human genes 0.000 description 1
108010076876 Keratins Proteins 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
239000000654 additive Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000004996 alkyl benzenes Chemical class 0.000 description 1
150000001347 alkyl bromides Chemical class 0.000 description 1
150000001350 alkyl halides Chemical class 0.000 description 1
150000001413 amino acids Chemical class 0.000 description 1
229910000148 ammonium phosphate Inorganic materials 0.000 description 1
235000019289 ammonium phosphates Nutrition 0.000 description 1
150000003863 ammonium salts Chemical class 0.000 description 1
239000001166 ammonium sulphate Substances 0.000 description 1
235000011130 ammonium sulphate Nutrition 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
JVQACSPNYXSVDE-UHFFFAOYSA-N azane;dodecyl hydrogen sulfate;sodium Chemical compound [NH4+].[Na].CCCCCCCCCCCCOS([O-])(=O)=O JVQACSPNYXSVDE-UHFFFAOYSA-N 0.000 description 1
235000010233 benzoic acid Nutrition 0.000 description 1
150000001559 benzoic acids Chemical class 0.000 description 1
125000003180 beta-lactone group Chemical group 0.000 description 1
VEZXCJBBBCKRPI-UHFFFAOYSA-N beta-propiolactone Chemical compound O=C1CCO1 VEZXCJBBBCKRPI-UHFFFAOYSA-N 0.000 description 1
239000008280 blood Substances 0.000 description 1
210000004369 blood Anatomy 0.000 description 1
239000010951 brass Substances 0.000 description 1
235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
235000010980 cellulose Nutrition 0.000 description 1
229920003086 cellulose ether Polymers 0.000 description 1
238000002485 combustion reaction Methods 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
239000012628 flowing agent Substances 0.000 description 1
150000002222 fluorine compounds Chemical class 0.000 description 1
238000009472 formulation Methods 0.000 description 1
239000007789 gas Substances 0.000 description 1
125000001145 hydrido group Chemical group *[H] 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
230000001771 impaired effect Effects 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
150000002596 lactones Chemical class 0.000 description 1
229920002521 macromolecule Polymers 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000004702 methyl esters Chemical class 0.000 description 1
239000004570 mortar (masonry) Substances 0.000 description 1
239000008239 natural water Substances 0.000 description 1
230000007935 neutral effect Effects 0.000 description 1
238000006386 neutralization reaction Methods 0.000 description 1
230000003472 neutralizing effect Effects 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
239000012038 nucleophile Substances 0.000 description 1
230000000269 nucleophilic effect Effects 0.000 description 1
150000002942 palmitic acid derivatives Chemical class 0.000 description 1
SNGREZUHAYWORS-UHFFFAOYSA-N perfluorooctanoic acid Chemical compound OC(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F SNGREZUHAYWORS-UHFFFAOYSA-N 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
229920000233 poly(alkylene oxides) Polymers 0.000 description 1
229920001515 polyalkylene glycol Polymers 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
239000011736 potassium bicarbonate Substances 0.000 description 1
229910000028 potassium bicarbonate Inorganic materials 0.000 description 1
239000001103 potassium chloride Substances 0.000 description 1
235000011164 potassium chloride Nutrition 0.000 description 1
OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
229910052939 potassium sulfate Inorganic materials 0.000 description 1
239000001120 potassium sulphate Substances 0.000 description 1
235000011151 potassium sulphates Nutrition 0.000 description 1
239000012254 powdered material Substances 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
239000003380 propellant Substances 0.000 description 1
229960000380 propiolactone Drugs 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
230000005855 radiation Effects 0.000 description 1
239000013535 sea water Substances 0.000 description 1
125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
239000000344 soap Substances 0.000 description 1
235000013024 sodium fluoride Nutrition 0.000 description 1
239000011775 sodium fluoride Substances 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
239000002904 solvent Substances 0.000 description 1
235000015096 spirit Nutrition 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
150000005621 tetraalkylammonium salts Chemical class 0.000 description 1
CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 1
125000003698 tetramethyl group Chemical group [H]C([H])([H])* 0.000 description 1
230000000007 visual effect Effects 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
- A62D1/0071—Foams
- A62D1/0085—Foams containing perfluoroalkyl-terminated surfactant

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)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)

IL32098A 1968-04-29 1969-04-29 Fire-fighting foam IL32098A (en)

Applications Claiming Priority (5)

Application Number	Priority Date	Filing Date	Title
GB5078768A GB1270661A (en)	1968-04-29	1968-04-29	Fire-fighting foams
GB2021468		1968-04-29
GB2161368		1968-05-07
GB4601368		1968-09-27
GB5078668		1968-10-25

Publications (2)

Publication Number	Publication Date
IL32098A0 IL32098A0 (en)	1969-06-25
IL32098A true IL32098A (en)	1972-07-26

Family

ID=27516214

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL32098A IL32098A (en)	1968-04-29	1969-04-29	Fire-fighting foam

Country Status (8)

Country	Link
BE (1)	BE732306A (de)
CH (1)	CH555683A (de)
DE (1)	DE1921928C3 (de)
FR (1)	FR2007254A1 (de)
IE (1)	IE33057B1 (de)
IL (1)	IL32098A (de)
NL (1)	NL6906538A (de)
SE (1)	SE382390B (de)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE765255A (fr) *	1970-04-22	1971-08-30	Ugine Kuhlmann	Composes fluores carboxyles ampholytes
JPS5815146B2 (ja) *	1978-10-14	1983-03-24	ダイキン工業株式会社	泡消火剤用添加剤
DE202014007301U1 (de)	2014-09-13	2015-12-16	Envites Energy Gesellschaft für Umwelttechnik und Energiesysteme mbH	Vorrichtung zur gefahrlosen Beherrschung eines Brandes oder Stoffaustrittes und der Verminderung seiner Ausbreitung und Auswirkungen
CN106075793A (zh) *	2016-06-22	2016-11-09	上海汇友精密化学品有限公司	一种抗冻型水成膜泡沫灭火剂的制备方法

1969
- 1969-04-16 IE IE506/69A patent/IE33057B1/xx unknown
- 1969-04-28 SE SE6906020A patent/SE382390B/xx unknown
- 1969-04-28 NL NL6906538A patent/NL6906538A/xx unknown
- 1969-04-29 BE BE732306D patent/BE732306A/xx unknown
- 1969-04-29 IL IL32098A patent/IL32098A/en unknown
- 1969-04-29 CH CH662669A patent/CH555683A/de not_active IP Right Cessation
- 1969-04-29 DE DE1921928A patent/DE1921928C3/de not_active Expired
- 1969-04-29 FR FR6913718A patent/FR2007254A1/fr not_active Withdrawn

Also Published As

Publication number	Publication date
IE33057L (en)	1969-10-29
FR2007254A1 (en)	1970-01-02
SE382390B (sv)	1976-02-02
BE732306A (de)	1969-10-29
DE1921928C3 (de)	1979-03-15
IL32098A0 (en)	1969-06-25
IE33057B1 (en)	1974-03-06
DE1921928A1 (de)	1969-11-20
CH555683A (de)	1974-11-15
NL6906538A (de)	1969-10-31
DE1921928B2 (de)	1978-07-13

Publication	Publication Date	Title
US5833874A (en)	1998-11-10	Fire extinguishing gels and methods of preparation and use thereof
EP0568601B1 (de)	1995-08-02	Wässrige, filmbildende, schäumbare lösung als feuerlöschmittelkonzentrat
US4099574A (en)	1978-07-11	Fire-fighting compositions
US4420434A (en)	1983-12-13	Perfluoralkyl anion/perfluoroalkyl cation ion pair complexes
US3258423A (en)	1966-06-28	Method of extinguishing liquid hydrocarbon fires
US3772195A (en)	1973-11-13	Fire extinguishing composition comprising a fluoroaliphatic surfactant fluorine-free surfactant
US4049556A (en)	1977-09-20	Foam fire extinguishing agent
US4472286A (en)	1984-09-18	Perfluoroalkyl anion/perfluoroalkyl cation ion pair complexes
US11577110B2 (en)	2023-02-14	Post-foaming composition for protection against fire and/or heat
CA2351344A1 (en)	2000-06-22	Aqueous foaming compositions, foam compositions, and preparation of foam compositions
US7135125B2 (en)	2006-11-14	Method of extinguishing or retarding fires
EP0120092B1 (de)	1987-04-08	Feuerlöschschaumzusammensetzung
WO2018066538A1 (ja)	2018-04-12	消火薬剤
JP4701470B2 (ja)	2011-06-15	消火薬剤
US4020903A (en)	1977-05-03	Fire-fighting foam compositions
IL32098A (en)	1972-07-26	Fire-fighting foam
EP0109046B1 (de)	1987-02-04	Feuerlöschzusammensetzung
JPH062169B2 (ja)	1994-01-12	水成泡消火薬剤
US20050051752A1 (en)	2005-03-10	Methods using fluorosulfones for extinguishing fire, preventing fire, and reducing or eliminating the flammability of a flammable working fluid
Tuve et al.	1964	A new vapor-securing agent for flammable-liquid fire extinguishment
CN102574783A (zh)	2012-07-11	氟化两性表面活性剂
EP2874713B1 (de)	2016-06-15	Verfahren zur herstellung von fluorierten betainen
CN112774076A (zh)	2021-05-11	一种泡沫灭火剂及其制备方法
AT306528B (de)	1973-04-10	Zusammensetzung zur Herstellung eines Schaumes zur Brandbekämpfung
JPS5838571A (ja)	1983-03-07	消火剤